Mlh3 Variant Search Result - Rat Genome Database

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1001 records found for search term Mlh3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155695245	CV1793932	single nucleotide variant	NM_001040108.2(MLH3):c.-3A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005370203]\|MLH3-related disorder [RCV003961002]\|not specified [RCV004050582]	likely benign\|uncertain significance	14	75049658	75049658	Human	1	name , alternate_id
155696409	CV1800720	single nucleotide variant	NM_001040108.2(MLH3):c.-5C>T	not specified [RCV004052555]	uncertain significance	14	75049660	75049660	Human		name
405268754	CV3201078	single nucleotide variant	NM_001040108.2(MLH3):c.*7A>T	MLH3-related disorder [RCV003899188]	likely benign	14	75017075	75017075	Human		name , trait , alternate_id
11634508	CV330629	single nucleotide variant	NM_001040108.2(MLH3):c.-4T>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000348165]\|not specified [RCV002268025]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75049659	75049659	Human	1	name
11664609	CV337252	single nucleotide variant	NM_001040108.2(MLH3):c.-27G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000407543]	uncertain significance	14	75049682	75049682	Human	1	name
598205394	CV3896826	single nucleotide variant	NM_001040108.2(MLH3):c.-15A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005357002]	uncertain significance	14	75049670	75049670	Human	1	name
11634495	CV321383	single nucleotide variant	NM_001040108.2(MLH3):c.*957C>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000283725]\|not provided [RCV004714850]	benign\|likely benign	14	75016125	75016125	Human	1	name
11634553	CV321407	single nucleotide variant	NM_001040108.1(MLH3):c.-204G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000402449]\|not provided [RCV001672502]	benign\|likely benign	14	75051520	75051520	Human	2	name
11634553	CV321407	single nucleotide variant	NM_001040108.1(MLH3):c.-204G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000402449]\|not provided [RCV001672502]	benign\|likely benign	14	75051520	75051521	Human	2	name
11634559	CV330633	single nucleotide variant	NM_001040108.2(MLH3):c.-133C>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000407550]	likely benign	14	75051449	75051449	Human	1	name
11659019	CV330636	single nucleotide variant	NM_001040108.1(MLH3):c.-202A>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000354132]	uncertain significance	14	75051518	75051518	Human	1	name
11634498	CV337229	single nucleotide variant	NM_001040108.2(MLH3):c.*958G>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000328148]\|not provided [RCV004714849]	benign\|likely benign	14	75016124	75016124	Human	1	name
11661025	CV337231	duplication	NM_001040108.2(MLH3):c.*797dup	Lynch syndrome [RCV000372750]	uncertain significance	14	75016284	75016285	Human	1	name
11634464	CV337237	single nucleotide variant	NM_001040108.2(MLH3):c.*772T>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000278070]	uncertain significance	14	75016310	75016310	Human	1	name
11656951	CV337238	single nucleotide variant	NM_001040108.2(MLH3):c.*744A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000337776]	uncertain significance	14	75016338	75016338	Human	1	name
11657572	CV337255	single nucleotide variant	NM_001040108.2(MLH3):c.-120G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000342194]	uncertain significance	14	75051436	75051436	Human	1	name
11651092	CV337260	single nucleotide variant	NM_001040108.2(MLH3):c.-149G>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000296948]	uncertain significance	14	75051465	75051465	Human	1	name
11651674	CV337269	single nucleotide variant	NM_001040108.1(MLH3):c.-208G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000300414]	uncertain significance	14	75051524	75051524	Human	1	name
11657430	CV339177	single nucleotide variant	NM_001040108.2(MLH3):c.*889G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000341396]	uncertain significance	14	75016193	75016193	Human	1	name
28878103	CV872657	single nucleotide variant	NM_001040108.2(MLH3):c.*888C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001116789]	uncertain significance	14	75016194	75016194	Human	1	name
28878106	CV872658	single nucleotide variant	NM_001040108.2(MLH3):c.*884C>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001116790]	uncertain significance	14	75016198	75016198	Human	1	name
28882788	CV872659	single nucleotide variant	NM_001040108.2(MLH3):c.*755T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001118240]	uncertain significance	14	75016327	75016327	Human	1	name
28882792	CV872660	single nucleotide variant	NM_001040108.2(MLH3):c.*646G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001118241]	uncertain significance	14	75016436	75016436	Human	1	name
28882796	CV872661	single nucleotide variant	NM_001040108.2(MLH3):c.*563A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001118242]	uncertain significance	14	75016519	75016519	Human	1	name
28882799	CV872662	single nucleotide variant	NM_001040108.2(MLH3):c.*541A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001118243]	uncertain significance	14	75016541	75016541	Human	1	name
28882802	CV872663	single nucleotide variant	NM_001040108.2(MLH3):c.*187T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001118244]	uncertain significance	14	75016895	75016895	Human	1	name
28889490	CV872673	single nucleotide variant	NM_001040108.2(MLH3):c.-124A>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001120275]	uncertain significance	14	75051440	75051440	Human	1	name
11665214	CV321373	single nucleotide variant	NM_001040108.2(MLH3):c.*3140C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001121567]\|Lynch syndrome [RCV000347337]\|Vanishing white matter disease [RCV000259710]	likely benign	14	75013942	75013942	Human	4	name
11660888	CV321378	single nucleotide variant	NM_001040108.2(MLH3):c.*1452G>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000371401]	uncertain significance	14	75015630	75015630	Human	1	name
11634469	CV321381	single nucleotide variant	NM_001040108.2(MLH3):c.*1376C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000276823]	uncertain significance	14	75015706	75015706	Human	1	name
11634538	CV330601	single nucleotide variant	NM_001040108.2(MLH3):c.*3105C>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000383201]	uncertain significance	14	75013977	75013977	Human	1	name
11648821	CV330608	deletion	NM_001040108.2(MLH3):c.*3048del	Lynch syndrome [RCV000284048]	uncertain significance	14	75014034	75014034	Human	1	name
11634577	CV330612	single nucleotide variant	NM_001040108.2(MLH3):c.*2590T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000403172]	likely benign\|uncertain significance	14	75014492	75014492	Human	1	name
11634540	CV330613	single nucleotide variant	NM_001040108.2(MLH3):c.*2174C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000336427]	likely benign\|uncertain significance	14	75014908	75014908	Human	1	name
11651837	CV330615	single nucleotide variant	NM_001040108.2(MLH3):c.*1990T>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000301410]	uncertain significance	14	75015092	75015092	Human	1	name
11634530	CV330619	single nucleotide variant	NM_001040108.2(MLH3):c.*1347T>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000327103]	likely benign\|uncertain significance	14	75015735	75015735	Human	1	name
11634534	CV330620	deletion	NM_001040108.2(MLH3):c.*1341del	Lynch syndrome [RCV000381745]	likely benign	14	75015741	75015741	Human	1	name
11634535	CV337218	single nucleotide variant	NM_001040108.2(MLH3):c.*3206C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000382067]	uncertain significance	14	75013876	75013876	Human	1	name
11665683	CV337219	single nucleotide variant	NM_001040108.2(MLH3):c.*3148A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001121566]\|Lynch syndrome [RCV000287442]\|Vanishing white matter disease [RCV000356812]\|not provided [RCV001683263]	benign\|likely benign	14	75013934	75013934	Human	4	name
11664211	CV337223	single nucleotide variant	NM_001040108.2(MLH3):c.*2086C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000403722]	uncertain significance	14	75014996	75014996	Human	1	name
11634473	CV337227	single nucleotide variant	NM_001040108.2(MLH3):c.*1877T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000275146]\|not provided [RCV004714848]	benign\|likely benign	14	75015205	75015205	Human	1	name
11666114	CV339151	single nucleotide variant	NM_001040108.2(MLH3):c.*2965C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001116684]\|Lynch syndrome [RCV000339142]\|Vanishing white matter disease [RCV000316823]\|not provided [RCV004703669]	benign\|likely benign	14	75014117	75014117	Human	4	name
11634478	CV339162	single nucleotide variant	NM_001040108.2(MLH3):c.*2417G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000304789]\|not provided [RCV004714847]	benign\|likely benign	14	75014665	75014665	Human	1	name
11634517	CV339163	single nucleotide variant	NM_001040108.2(MLH3):c.*1896A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000356232]\|not provided [RCV004703670]	likely benign	14	75015186	75015186	Human	1	name
11653501	CV339170	deletion	NM_001040108.2(MLH3):c.*1701del	Lynch syndrome [RCV000311505]	uncertain significance	14	75015381	75015381	Human	1	name
11634483	CV339171	single nucleotide variant	NM_001040108.2(MLH3):c.*1237A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000273123]	likely benign\|uncertain significance	14	75015845	75015845	Human	1	name
28893090	CV872632	single nucleotide variant	NM_001040108.2(MLH3):c.*3258T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001121565]	uncertain significance	14	75013824	75013824	Human	1	name
28893094	CV872633	single nucleotide variant	NM_001040108.2(MLH3):c.*3140C>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001121568]	uncertain significance	14	75013942	75013942	Human	1	name
28893097	CV872634	single nucleotide variant	NM_001040108.2(MLH3):c.*3094C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001121569]	uncertain significance	14	75013988	75013988	Human	1	name
28877777	CV872635	single nucleotide variant	NM_001040108.2(MLH3):c.*3047G>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001116683]	uncertain significance	14	75014035	75014035	Human	1	name
28877782	CV872636	single nucleotide variant	NM_001040108.2(MLH3):c.*2679A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001116685]	uncertain significance	14	75014403	75014403	Human	1	name
28877787	CV872637	single nucleotide variant	NM_001040108.2(MLH3):c.*2495C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001116686]	uncertain significance	14	75014587	75014587	Human	1	name
28877789	CV872638	single nucleotide variant	NM_001040108.2(MLH3):c.*2470C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001116687]	uncertain significance	14	75014612	75014612	Human	1	name
28877793	CV872639	single nucleotide variant	NM_001040108.2(MLH3):c.*2469A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001116688]	uncertain significance	14	75014613	75014613	Human	1	name
28882443	CV872640	single nucleotide variant	NM_001040108.2(MLH3):c.*2407T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001118133]	likely benign	14	75014675	75014675	Human	1	name
28882448	CV872641	single nucleotide variant	NM_001040108.2(MLH3):c.*2398C>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001118134]	uncertain significance	14	75014684	75014684	Human	1	name
28882449	CV872642	single nucleotide variant	NM_001040108.2(MLH3):c.*2058G>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001118135]\|not provided [RCV003393855]	benign\|uncertain significance	14	75015024	75015024	Human	1	name
28887586	CV872643	single nucleotide variant	NM_001040108.2(MLH3):c.*1767G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001119672]	likely benign	14	75015315	75015315	Human	1	name
28887589	CV872644	single nucleotide variant	NM_001040108.2(MLH3):c.*1674T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001119673]	uncertain significance	14	75015408	75015408	Human	1	name
28887592	CV872645	single nucleotide variant	NM_001040108.2(MLH3):c.*1628G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001119674]	uncertain significance	14	75015454	75015454	Human	1	name
28887596	CV872646	single nucleotide variant	NM_001040108.2(MLH3):c.*1566G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001119675]	uncertain significance	14	75015516	75015516	Human	1	name
28887598	CV872647	single nucleotide variant	NM_001040108.2(MLH3):c.*1470C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001119676]	uncertain significance	14	75015612	75015612	Human	1	name
28887602	CV872648	single nucleotide variant	NM_001040108.2(MLH3):c.*1448G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001119677]	uncertain significance	14	75015634	75015634	Human	1	name
28887604	CV872649	single nucleotide variant	NM_001040108.2(MLH3):c.*1447C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001119678]	uncertain significance	14	75015635	75015635	Human	1	name
28893342	CV872650	single nucleotide variant	NM_001040108.2(MLH3):c.*1381T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001121660]	uncertain significance	14	75015701	75015701	Human	1	name
28893346	CV872651	single nucleotide variant	NM_001040108.2(MLH3):c.*1312G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001121661]	uncertain significance	14	75015770	75015770	Human	1	name
28893349	CV872652	single nucleotide variant	NM_001040108.2(MLH3):c.*1291G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001121662]	uncertain significance	14	75015791	75015791	Human	1	name
28893354	CV872653	single nucleotide variant	NM_001040108.2(MLH3):c.*1235T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001121663]	uncertain significance	14	75015847	75015847	Human	1	name
28893356	CV872654	single nucleotide variant	NM_001040108.2(MLH3):c.*1159A>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001121664]	uncertain significance	14	75015923	75015923	Human	1	name
28878095	CV872655	single nucleotide variant	NM_001040108.2(MLH3):c.*1110T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001116787]	uncertain significance	14	75015972	75015972	Human	1	name
28878099	CV872656	single nucleotide variant	NM_001040108.2(MLH3):c.*1073A>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001116788]	uncertain significance	14	75016009	75016009	Human	1	name
127247257	CV1102547	single nucleotide variant	NM_001040108.2(MLH3):c.3644-6A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001424658]	likely benign	14	75033496	75033496	Human	1	name
127244908	CV1102548	single nucleotide variant	NM_001040108.2(MLH3):c.3281-8A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001424188]	likely benign	14	75042485	75042485	Human	1	name
127243732	CV1102550	single nucleotide variant	NM_001040108.2(MLH3):c.3280+9G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001434888]\|MLH3-related disorder [RCV003920935]\|not specified [RCV002268487]	likely benign	14	75046367	75046367	Human	1	name , alternate_id
127308259	CV1144829	single nucleotide variant	NM_001040108.2(MLH3):c.3644-5T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001480576]\|not specified [RCV004037207]	likely benign\|uncertain significance	14	75033495	75033495	Human	1	name
151757597	CV1438754	single nucleotide variant	NM_001040108.2(MLH3):c.3570+9T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002007493]	likely benign	14	75039902	75039902	Human	1	name
151881384	CV1499872	single nucleotide variant	NM_001040108.2(MLH3):c.3643+5G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001886531]\|not specified [RCV004041211]	uncertain significance	14	75038335	75038335	Human	1	name
152149697	CV1601411	single nucleotide variant	NM_001040108.2(MLH3):c.3716-4A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002157986]\|Endometrial carcinoma [RCV005008468]\|MLH3-related disorder [RCV004752160]\|not specified [RCV004046395]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75032183	75032183	Human	5	name , alternate_id
152105512	CV1614693	deletion	NM_001040108.2(MLH3):c.3827+9del	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002079554]	likely benign	14	75032059	75032059	Human	1	name
152107182	CV1657264	single nucleotide variant	NM_001040108.2(MLH3):c.3715+8T>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002214975]	likely benign	14	75033411	75033411	Human	1	name
153303007	CV1690063	single nucleotide variant	NM_001040108.2(MLH3):c.4091-6A>T	not specified [RCV002268963]	likely benign	14	75018986	75018986	Human		name
153303021	CV1690074	single nucleotide variant	NM_001040108.2(MLH3):c.3643+8T>C	not specified [RCV002268974]	likely benign	14	75038332	75038332	Human		name
155664804	CV1786655	single nucleotide variant	NM_001040108.2(MLH3):c.3716-1G>A	not provided [RCV004546717]\|not specified [RCV004049748]	pathogenic\|uncertain significance	14	75032180	75032180	Human		name
155733462	CV1788005	single nucleotide variant	NM_001040108.2(MLH3):c.4242+5A>G	not specified [RCV004051957]	uncertain significance	14	75018824	75018824	Human		name
155686213	CV1789807	single nucleotide variant	NM_001040108.2(MLH3):c.3828-5T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005096409]\|not specified [RCV004048169]	likely benign\|uncertain significance	14	75030707	75030707	Human	1	name
156396739	CV1870893	single nucleotide variant	NM_001040108.2(MLH3):c.3465+9G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003068683]	likely benign	14	75041606	75041606	Human	1	name
156283736	CV1877255	single nucleotide variant	NM_001040108.2(MLH3):c.3465+3G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003061161]	uncertain significance	14	75041612	75041612	Human	1	name
155967127	CV1892366	single nucleotide variant	NM_001040108.2(MLH3):c.3281-7T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003074989]	likely benign	14	75042484	75042484	Human	1	name
155957084	CV2033477	single nucleotide variant	NM_001040108.2(MLH3):c.3644-7C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002730984]	likely benign	14	75033497	75033497	Human	1	name
156299273	CV2104844	single nucleotide variant	NM_001040108.2(MLH3):c.3379+4A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002922495]	uncertain significance	14	75042375	75042375	Human	1	name
156324701	CV2134430	single nucleotide variant	NM_001040108.2(MLH3):c.3571-1G>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002963445]\|not specified [RCV004632125]	uncertain significance	14	75038413	75038413	Human	1	name
329363675	CV2425903	single nucleotide variant	NM_001040108.2(MLH3):c.4242+3A>C	not specified [RCV004243272]	uncertain significance	14	75018826	75018826	Human		name
329390024	CV2465720	single nucleotide variant	NM_001040108.2(MLH3):c.3379+5G>T	not specified [RCV004281539]	uncertain significance	14	75042374	75042374	Human		name
401798299	CV2741381	single nucleotide variant	NM_001040108.2(MLH3):c.4011+3A>C	not specified [RCV003322544]	uncertain significance	14	75022992	75022992	Human		name
405006093	CV2852941	single nucleotide variant	NM_001040108.2(MLH3):c.3827+7A>G	not specified [RCV003494135]	likely benign	14	75032061	75032061	Human		name
402479638	CV2889090	single nucleotide variant	NM_001040108.2(MLH3):c.4090+7C>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003506315]	likely benign	14	75022807	75022807	Human	1	name
402472500	CV2917233	single nucleotide variant	NM_001040108.2(MLH3):c.3466-2A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003504916]	uncertain significance	14	75040017	75040017	Human	1	name
405096306	CV2946732	single nucleotide variant	NM_001040108.2(MLH3):c.3465+4G>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003614261]	uncertain significance	14	75041611	75041611	Human	1	name
405107344	CV3014367	single nucleotide variant	NM_001040108.2(MLH3):c.3571-9G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003614818]	likely benign	14	75038421	75038421	Human	1	name
405109793	CV3058905	single nucleotide variant	NM_001040108.2(MLH3):c.3828-7T>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003615332]	uncertain significance	14	75030709	75030709	Human	1	name
405109713	CV3068707	single nucleotide variant	NM_001040108.2(MLH3):c.3827+1G>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003615318]	uncertain significance	14	75032067	75032067	Human	1	name
11634557	CV321389	single nucleotide variant	NM_001040108.2(MLH3):c.3987+7C>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000405862]\|Endometrial carcinoma [RCV005235254]\|not provided [RCV001653544]\|not specified [RCV002268021]	benign\|likely benign	14	75030536	75030536	Human	3	name
11648965	CV330631	duplication	NM_001040108.2(MLH3):c.-63-10dup	Lynch syndrome [RCV000284853]	uncertain significance	14	75049727	75049728	Human	1	name
405702533	CV3392333	single nucleotide variant	NM_001040108.2(MLH3):c.3281-5T>G	not specified [RCV004521207]	uncertain significance	14	75042482	75042482	Human		name
405702594	CV3392342	single nucleotide variant	NM_001040108.2(MLH3):c.3379+3A>G	not specified [RCV004521216]	uncertain significance	14	75042376	75042376	Human		name
405702668	CV3392352	single nucleotide variant	NM_001040108.2(MLH3):c.3644-3T>C	not specified [RCV004521226]	uncertain significance	14	75033493	75033493	Human		name
597636340	CV3556978	single nucleotide variant	NM_001040108.2(MLH3):c.3465+3G>T	not specified [RCV004824516]	uncertain significance	14	75041612	75041612	Human		name
597640983	CV3556999	single nucleotide variant	NM_001040108.2(MLH3):c.3380-2A>G	not specified [RCV004825379]	uncertain significance	14	75041702	75041702	Human		name
597641009	CV3557007	single nucleotide variant	NM_001040108.2(MLH3):c.3987+4A>G	not specified [RCV004825385]	uncertain significance	14	75030539	75030539	Human		name
597636383	CV3557018	single nucleotide variant	NM_001040108.2(MLH3):c.4243-4A>G	not specified [RCV004824524]	likely benign	14	75017205	75017205	Human		name
597641194	CV3557062	single nucleotide variant	NM_001040108.2(MLH3):c.4243-3T>C	not specified [RCV004825417]	uncertain significance	14	75017204	75017204	Human		name
597689963	CV3710973	single nucleotide variant	NM_001040108.2(MLH3):c.3827+5G>A	Endometrial carcinoma [RCV005007298]	uncertain significance	14	75032063	75032063	Human	2	name
597916810	CV3767743	single nucleotide variant	NM_001040108.2(MLH3):c.3280+3A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005114544]	uncertain significance	14	75046373	75046373	Human	1	name
597842201	CV3822039	single nucleotide variant	NM_001040108.2(MLH3):c.3644-8T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005172353]	likely benign	14	75033498	75033498	Human	1	name
597871125	CV3835653	single nucleotide variant	NM_001040108.2(MLH3):c.3570+5A>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005176644]	uncertain significance	14	75039906	75039906	Human	1	name
598124319	CV3881458	single nucleotide variant	NM_001040108.2(MLH3):c.3465+4G>A	not specified [RCV005231883]	likely benign	14	75041611	75041611	Human		name
598187735	CV3989364	single nucleotide variant	NM_001040108.2(MLH3):c.3988-1G>A	not specified [RCV005373609]	uncertain significance	14	75023019	75023019	Human		name
598166808	CV3989421	single nucleotide variant	NM_001040108.2(MLH3):c.4091-1G>A	not specified [RCV005369400]	uncertain significance	14	75018981	75018981	Human		name
13626804	CV528283	single nucleotide variant	NM_001040108.2(MLH3):c.4091-2A>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000779147]\|not specified [RCV004025958]	uncertain significance	14	75018982	75018982	Human	1	name
13626831	CV528725	single nucleotide variant	NM_001040108.2(MLH3):c.3280+8C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000655408]	likely benign	14	75046368	75046368	Human	1	name
13674104	CV536118	single nucleotide variant	NM_001040108.2(MLH3):c.3643+2T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001855348]\|Endometrial carcinoma [RCV005010637]\|not provided [RCV000656579]	likely pathogenic\|uncertain significance	14	75038338	75038338	Human	4	name
14719099	CV652971	single nucleotide variant	NM_001040108.2(MLH3):c.3715+1G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000796021]	uncertain significance	14	75033418	75033418	Human	1	name
14738278	CV652974	single nucleotide variant	NM_001040108.2(MLH3):c.3643+4A>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000804434]\|not specified [RCV004028175]	uncertain significance	14	75038336	75038336	Human	1	name
15103833	CV690090	single nucleotide variant	NM_001040108.2(MLH3):c.3571-9G>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001436697]	likely benign	14	75038421	75038421	Human	1	name
15107474	CV776305	single nucleotide variant	NM_001040108.2(MLH3):c.3281-8A>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000937976]	likely benign	14	75042485	75042485	Human	1	name
38475364	CV940314	single nucleotide variant	NM_001040108.2(MLH3):c.4090+2T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001204244]\|not specified [RCV004033607]	uncertain significance	14	75022812	75022812	Human	1	name
38458111	CV940315	single nucleotide variant	NM_001040108.2(MLH3):c.3379+4A>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001211326]	uncertain significance	14	75042375	75042375	Human	1	name
126734898	CV995963	single nucleotide variant	NM_001040108.2(MLH3):c.3280+4A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001304519]\|not specified [RCV004036313]	uncertain significance	14	75046372	75046372	Human	1	name
127255260	CV1080723	single nucleotide variant	NM_001040108.2(MLH3):c.3380-10T>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001418708]	likely benign	14	75041710	75041710	Human	1	name
127267005	CV1102549	single nucleotide variant	NM_001040108.2(MLH3):c.3280+10T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001429533]	likely benign	14	75046366	75046366	Human	1	name
150469710	CV1219119	deletion	NM_001040108.2(MLH3):c.3465+37del	not provided [RCV001614871]\|not specified [RCV002268538]	benign	14	75041578	75041578	Human		name
150453182	CV1231795	single nucleotide variant	NM_001040108.2(MLH3):c.4012-37G>A	not provided [RCV001648102]	benign	14	75022929	75022929	Human		name
150458349	CV1248919	single nucleotide variant	NM_001040108.2(MLH3):c.3379+38A>G	not provided [RCV001669095]\|not specified [RCV002268552]	benign	14	75042341	75042341	Human		name
150469384	CV1259649	single nucleotide variant	NM_001040108.2(MLH3):c.4090+71A>G	not provided [RCV001683950]	benign	14	75022743	75022743	Human		name
150498624	CV1282163	single nucleotide variant	NM_001040108.2(MLH3):c.3643+27T>C	not provided [RCV001718051]	benign	14	75038313	75038313	Human		name
150493721	CV1282165	single nucleotide variant	NM_001040108.2(MLH3):c.3643+35C>G	not provided [RCV001717065]	benign	14	75038305	75038305	Human		name
150493731	CV1282168	single nucleotide variant	NM_001040108.2(MLH3):c.4242+43T>C	not provided [RCV001717067]	benign	14	75018786	75018786	Human		name
152175176	CV1520736	deletion	NM_001040108.2(MLH3):c.4090+10del	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002184764]	likely benign	14	75022804	75022804	Human	1	name
152077779	CV1531375	single nucleotide variant	NM_001040108.2(MLH3):c.4012-18A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002210823]	likely benign	14	75022910	75022910	Human	1	name
152069057	CV1569872	single nucleotide variant	NM_001040108.2(MLH3):c.3280+20G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002191534]	likely benign	14	75046356	75046356	Human	1	name
152067205	CV1579178	duplication	NM_001040108.2(MLH3):c.4242+14dup	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002074611]	likely benign	14	75018814	75018815	Human	1	name
152132959	CV1585171	single nucleotide variant	NM_001040108.2(MLH3):c.4091-13G>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002083119]	likely benign	14	75018993	75018993	Human	1	name
152098248	CV1627037	single nucleotide variant	NM_001040108.2(MLH3):c.3280+19T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002095155]\|not specified [RCV002268611]	likely benign	14	75046357	75046357	Human	1	name
152101546	CV1645842	single nucleotide variant	NM_001040108.2(MLH3):c.3827+19A>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002173171]	likely benign	14	75032049	75032049	Human	1	name
152055676	CV1662688	single nucleotide variant	NM_001040108.2(MLH3):c.4011+15T>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002146192]\|Endometrial carcinoma [RCV002500326]\|not specified [RCV003321911]	benign\|likely benign	14	75022980	75022980	Human	4	name
153303009	CV1690064	single nucleotide variant	NM_001040108.2(MLH3):c.4012-16C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003101531]\|not specified [RCV002268964]	likely benign	14	75022908	75022908	Human	1	name
153303010	CV1690065	single nucleotide variant	NM_001040108.2(MLH3):c.3988-14C>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003096085]\|not specified [RCV002268965]	likely benign	14	75023032	75023032	Human	1	name
153303011	CV1690066	single nucleotide variant	NM_001040108.2(MLH3):c.3988-35C>T	not specified [RCV002268966]	benign	14	75023053	75023053	Human		name
153303012	CV1690067	single nucleotide variant	NM_001040108.2(MLH3):c.3987+12C>A	not specified [RCV002268967]	likely benign	14	75030531	75030531	Human		name
153303014	CV1690068	duplication	NM_001040108.2(MLH3):c.3828-24dup	not specified [RCV002268968]	likely benign	14	75030725	75030726	Human		name
153303015	CV1690069	single nucleotide variant	NM_001040108.2(MLH3):c.3827+44C>T	not specified [RCV002268969]	benign	14	75032024	75032024	Human		name
153303016	CV1690070	single nucleotide variant	NM_001040108.2(MLH3):c.3827+39A>G	not specified [RCV002268970]	likely benign	14	75032029	75032029	Human		name
153303018	CV1690072	single nucleotide variant	NM_001040108.2(MLH3):c.3644-43G>A	not specified [RCV002268972]	likely benign	14	75033533	75033533	Human		name
153303020	CV1690073	single nucleotide variant	NM_001040108.2(MLH3):c.3643+33A>G	not specified [RCV002268973]	likely benign	14	75038307	75038307	Human		name
153303028	CV1690080	single nucleotide variant	NM_001040108.2(MLH3):c.3465+50C>A	not specified [RCV002268980]	likely benign	14	75041565	75041565	Human		name
153303029	CV1690081	duplication	NM_001040108.2(MLH3):c.3465+37dup	not specified [RCV002268981]	likely benign	14	75041577	75041578	Human		name
155799566	CV1859885	single nucleotide variant	NM_001040108.2(MLH3):c.4091-39A>G	not specified [RCV002466129]	likely benign	14	75019019	75019019	Human		name
155799568	CV1859886	single nucleotide variant	NM_001040108.2(MLH3):c.4090+38C>T	not specified [RCV002466130]	benign	14	75022776	75022776	Human		name
155799577	CV1859890	single nucleotide variant	NM_001040108.2(MLH3):c.3379+40C>T	not provided [RCV004703276]\|not specified [RCV002466134]	likely benign	14	75042339	75042339	Human		name
156375267	CV1871991	single nucleotide variant	NM_001040108.2(MLH3):c.3715+18G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003066662]	likely benign	14	75033401	75033401	Human	1	name
156357397	CV1877627	single nucleotide variant	NM_001040108.2(MLH3):c.4012-15G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003065352]	likely benign	14	75022907	75022907	Human	1	name
156372567	CV1878474	single nucleotide variant	NM_001040108.2(MLH3):c.3571-15T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003066423]	likely benign	14	75038427	75038427	Human	1	name
156416350	CV1904973	single nucleotide variant	NM_001040108.2(MLH3):c.3827+20T>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002610127]	uncertain significance	14	75032048	75032048	Human	1	name
156442313	CV1938542	single nucleotide variant	NM_001040108.2(MLH3):c.4243-10C>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003112654]	likely benign	14	75017211	75017211	Human	1	name
156434537	CV1940077	single nucleotide variant	NM_001040108.2(MLH3):c.4243-15T>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003104493]	likely benign	14	75017216	75017216	Human	1	name
156398717	CV1982046	single nucleotide variant	NM_001040108.2(MLH3):c.3643+16A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002635764]\|not specified [RCV004596558]	likely benign	14	75038324	75038324	Human	1	name
156011452	CV2016694	single nucleotide variant	NM_001040108.2(MLH3):c.3380-17G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002734917]	likely benign	14	75041717	75041717	Human	1	name
156047332	CV2059900	single nucleotide variant	NM_001040108.2(MLH3):c.3716-16A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002796649]	likely benign	14	75032195	75032195	Human	1	name
155975231	CV2150952	single nucleotide variant	NM_001040108.2(MLH3):c.3380-12C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003033618]	likely benign	14	75041712	75041712	Human	1	name
155918055	CV2152491	single nucleotide variant	NM_001040108.2(MLH3):c.3379+20C>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002991759]	likely benign	14	75042359	75042359	Human	1	name
401796031	CV2740091	single nucleotide variant	NM_001040108.2(MLH3):c.3465+37T>C	not specified [RCV003320326]	likely benign	14	75041578	75041578	Human		name
401798301	CV2741382	single nucleotide variant	NM_001040108.2(MLH3):c.3716-24A>G	not specified [RCV003322545]	benign	14	75032203	75032203	Human		name
401798302	CV2741383	single nucleotide variant	NM_001040108.2(MLH3):c.3643+25G>A	not specified [RCV003322546]	likely benign	14	75038315	75038315	Human		name
405006084	CV2852940	single nucleotide variant	NM_001040108.2(MLH3):c.3988-34G>A	not specified [RCV003494134]	likely benign	14	75023052	75023052	Human		name
405006104	CV2852942	single nucleotide variant	NM_001040108.2(MLH3):c.3644-25A>G	not specified [RCV003494136]	likely benign	14	75033515	75033515	Human		name
405006112	CV2852943	single nucleotide variant	NM_001040108.2(MLH3):c.3643+44T>C	not specified [RCV003494137]	likely benign	14	75038296	75038296	Human		name
402481393	CV2898127	single nucleotide variant	NM_001040108.2(MLH3):c.3644-20C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003506528]	likely benign	14	75033510	75033510	Human	1	name
402471236	CV2901203	single nucleotide variant	NM_001040108.2(MLH3):c.4011+10T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003504619]	likely benign	14	75022985	75022985	Human	1	name
405107439	CV3016277	single nucleotide variant	NM_001040108.2(MLH3):c.4243-16T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003614738]	likely benign	14	75017217	75017217	Human	1	name
405108302	CV3035232	single nucleotide variant	NM_001040108.2(MLH3):c.3280+14A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003615031]	likely benign	14	75046362	75046362	Human	1	name
405109540	CV3058050	single nucleotide variant	NM_001040108.2(MLH3):c.4090+18G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003615286]	likely benign	14	75022796	75022796	Human	1	name
405110478	CV3065857	single nucleotide variant	NM_001040108.2(MLH3):c.3715+10T>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003615357]	likely benign	14	75033409	75033409	Human	1	name
405111851	CV3077566	single nucleotide variant	NM_001040108.2(MLH3):c.3715+16C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003615504]	likely benign	14	75033403	75033403	Human	1	name
405122987	CV3131729	single nucleotide variant	NM_001040108.2(MLH3):c.3644-16A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003837593]	likely benign	14	75033506	75033506	Human	1	name
405109078	CV3136705	single nucleotide variant	NM_001040108.2(MLH3):c.3827+11C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003835859]\|not specified [RCV004596609]	benign\|likely benign	14	75032057	75032057	Human	1	name
11634521	CV337240	single nucleotide variant	NM_001040108.2(MLH3):c.4242+13C>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000312351]\|Endometrial carcinoma [RCV005235253]\|not provided [RCV003736709]\|not specified [RCV000584456]	benign\|likely benign	14	75018816	75018816	Human	3	name
11634509	CV339184	single nucleotide variant	NM_001040108.2(MLH3):c.3987+15C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000348406]\|not provided [RCV001573906]\|not specified [RCV000581638]	benign\|likely benign\|uncertain significance	14	75030528	75030528	Human	1	name
11634454	CV339189	single nucleotide variant	NM_001040108.2(MLH3):c.3280+14A>T	Colorectal cancer [RCV005355638]\|Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000264615]\|not specified [RCV004596160]	benign\|likely benign\|uncertain significance	14	75046362	75046362	Human	3	name
407489768	CV3415036	single nucleotide variant	NM_001040108.2(MLH3):c.4242+40T>C	not specified [RCV004597371]	likely benign	14	75018789	75018789	Human		name
407489751	CV3415038	single nucleotide variant	NM_001040108.2(MLH3):c.3465+38C>T	not specified [RCV004597373]	likely benign	14	75041577	75041577	Human		name
597958870	CV3751995	single nucleotide variant	NM_001040108.2(MLH3):c.4011+12C>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005081125]	likely benign	14	75022983	75022983	Human	1	name
597963593	CV3792001	single nucleotide variant	NM_001040108.2(MLH3):c.3827+13A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005139557]	likely benign	14	75032055	75032055	Human	1	name
597866652	CV3802870	single nucleotide variant	NM_001040108.2(MLH3):c.3716-16A>C	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005147657]	likely benign	14	75032195	75032195	Human	1	name
597842076	CV3825643	single nucleotide variant	NM_001040108.2(MLH3):c.3280+18A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005172326]	likely benign	14	75046358	75046358	Human	1	name
597901310	CV3835511	single nucleotide variant	NM_001040108.2(MLH3):c.3988-20A>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005181235]	likely benign	14	75023038	75023038	Human	1	name
597931244	CV3837483	single nucleotide variant	NM_001040108.2(MLH3):c.4242+17C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005185641]	likely benign	14	75018812	75018812	Human	1	name
598124316	CV3881457	single nucleotide variant	NM_001040108.2(MLH3):c.4011+46A>G	not specified [RCV005231882]	likely benign	14	75022949	75022949	Human		name
598124322	CV3881459	single nucleotide variant	NM_001040108.2(MLH3):c.3281-35G>T	not specified [RCV005231884]	likely benign	14	75042512	75042512	Human		name
598226740	CV3895844	single nucleotide variant	NM_001040108.2(MLH3):c.3380-14C>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005362135]	likely benign	14	75041714	75041714	Human	1	name
13499666	CV464361	single nucleotide variant	NM_001040108.2(MLH3):c.3643+10G>A	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000539959]	likely benign	14	75038330	75038330	Human	1	name
13512144	CV485654	single nucleotide variant	NM_001040108.2(MLH3):c.4242+28G>C	not specified [RCV000583246]	likely benign	14	75018801	75018801	Human		name
13512119	CV485655	single nucleotide variant	NM_001040108.2(MLH3):c.3828-15A>C	not specified [RCV000583210]	likely benign	14	75030717	75030717	Human		name
13513043	CV485656	deletion	NM_001040108.2(MLH3):c.3828-24del	not specified [RCV000584449]	likely benign	14	75030726	75030726	Human		name
13511178	CV485657	single nucleotide variant	NM_001040108.2(MLH3):c.3716-10C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002061964]\|not specified [RCV000582048]	likely benign	14	75032189	75032189	Human	1	name
13512113	CV485658	single nucleotide variant	NM_001040108.2(MLH3):c.3571-26G>T	not specified [RCV000583304]	likely benign	14	75038438	75038438	Human		name
13513014	CV485659	single nucleotide variant	NM_001040108.2(MLH3):c.3570+28A>T	not specified [RCV000584520]	benign\|likely benign	14	75039883	75039883	Human		name
28893589	CV876449	single nucleotide variant	NM_001040108.2(MLH3):c.3644-13C>T	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001121763]\|not specified [RCV003493802]	benign\|likely benign	14	75033503	75033503	Human	1	name
28893592	CV876450	single nucleotide variant	NM_001040108.2(MLH3):c.3465+14A>G	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001121765]	uncertain significance	14	75041601	75041601	Human	1	name
150487343	CV1225893	single nucleotide variant	NM_001040108.2(MLH3):c.4243-153A>G	not provided [RCV001618054]	benign	14	75017354	75017354	Human		name
150510112	CV1248517	single nucleotide variant	NM_001040108.2(MLH3):c.3466-157C>T	not provided [RCV001659586]	benign	14	75040172	75040172	Human		name
150468261	CV1259475	single nucleotide variant	NM_001040108.2(MLH3):c.3987+116G>T	not provided [RCV001683774]	benign	14	75030427	75030427	Human		name
150497957	CV1281671	single nucleotide variant	NM_001040108.2(MLH3):c.3280+165G>A	not provided [RCV001717935]	benign	14	75046211	75046211	Human		name
150479102	CV1282169	single nucleotide variant	NM_001040108.2(MLH3):c.4242+126C>T	not provided [RCV001714410]	benign	14	75018703	75018703	Human		name
153303022	CV1690075	microsatellite	NM_001040108.2(MLH3):c.3570+29AT[9]	not specified [RCV002268975]	benign	14	75039847	75039864	Human		name
155265023	CV1695414	microsatellite	NM_001040108.2(MLH3):c.3570+29AT[7]	not specified [RCV002279989]	likely benign	14	75039847	75039868	Human		name
155265025	CV1695417	microsatellite	NM_001040108.2(MLH3):c.3570+29AT[8]	not specified [RCV002279992]	likely benign	14	75039847	75039866	Human		name
150452202	CV1231674	microsatellite	NM_001040108.2(MLH3):c.3570+29AT[22]	not provided [RCV001647980]	benign	14	75039846	75039847	Human		name
150466360	CV1255726	microsatellite	NM_001040108.2(MLH3):c.3570+29AT[21]	not provided [RCV001670360]	benign	14	75039846	75039847	Human		name
150507908	CV1257257	microsatellite	NM_001040108.2(MLH3):c.3465+38CTT[4]	not provided [RCV001678556]\|not specified [RCV002268557]	benign	14	75041563	75041565	Human		name
150479092	CV1282164	microsatellite	NM_001040108.2(MLH3):c.3570+29AT[10]	not provided [RCV001714408]\|not specified [RCV002279976]	benign\|likely benign	14	75039847	75039862	Human		name
155265020	CV1695412	microsatellite	NM_001040108.2(MLH3):c.3570+29AT[24]	not specified [RCV002279987]	likely benign	14	75039846	75039847	Human		name
155265021	CV1695413	microsatellite	NM_001040108.2(MLH3):c.3570+29AT[23]	not specified [RCV002279988]	likely benign	14	75039846	75039847	Human		name
150434924	CV1231213	microsatellite	NM_001040108.2(MLH3):c.3570+124GT[13]	not provided [RCV001643858]	benign	14	75039760	75039761	Human		name
150498808	CV1282284	microsatellite	NM_001040108.2(MLH3):c.3570+124GT[12]	not provided [RCV001718082]	benign	14	75039760	75039763	Human		name
405193450	CV3128488	duplication	NM_001040108.2(MLH3):c.4238_4242+1dup	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003821225]	uncertain significance	14	75018827	75018828	Human	1	name
407486797	CV3457339	deletion	NM_001040108.2(MLH3):c.4012-5_4048del	not specified [RCV004640948]	uncertain significance	14	75022856	75022897	Human		name
155719512	CV1837380	single nucleotide variant	NM_001040108.2(MLH3):c.15G>A (p.Leu5=)	not specified [RCV004057417]	likely benign	14	75049641	75049641	Human		name
155686489	CV1852597	single nucleotide variant	NM_001040108.2(MLH3):c.27A>T (p.Val9=)	not specified [RCV004062251]	likely benign	14	75049629	75049629	Human		name
329364691	CV2425914	single nucleotide variant	NM_001040108.2(MLH3):c.18A>C (p.Ser6=)	not specified [RCV004243283]	likely benign	14	75049638	75049638	Human		name
597640914	CV3556976	single nucleotide variant	NM_001040108.2(MLH3):c.12C>T (p.Cys4=)	not specified [RCV004825367]	likely benign	14	75049644	75049644	Human		name
598201266	CV4007585	duplication	NM_001040108.2(MLH3):c.3466-19_3569dup	Endometrial carcinoma [RCV005398417]	uncertain significance	14	75039911	75039912	Human	2	name
127258029	CV1102556	single nucleotide variant	NM_001040108.2(MLH3):c.45T>G (p.Ser15=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001438004]\|not specified [RCV004038359]	likely benign	14	75049611	75049611	Human	1	name
127312086	CV1144844	single nucleotide variant	NM_001040108.2(MLH3):c.96C>T (p.Asn32=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001481603]\|not specified [RCV004037215]	likely benign	14	75049560	75049560	Human	1	name
155685612	CV1793400	single nucleotide variant	NM_001040108.2(MLH3):c.37T>C (p.Leu13=)	not specified [RCV004048116]	likely benign	14	75049619	75049619	Human		name
155725948	CV1799616	single nucleotide variant	NM_001040108.2(MLH3):c.51G>A (p.Leu17=)	not specified [RCV004051685]	likely benign	14	75049605	75049605	Human		name
155740554	CV1809459	single nucleotide variant	NM_001040108.2(MLH3):c.4A>G (p.Ile2Val)	not specified [RCV004050872]	uncertain significance	14	75049652	75049652	Human		name
155705461	CV1811215	single nucleotide variant	NM_001040108.2(MLH3):c.60C>T (p.Ser20=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003103264]\|not specified [RCV004052724]	likely benign	14	75049596	75049596	Human	1	name
156037182	CV2052582	single nucleotide variant	NM_001040108.2(MLH3):c.1A>G (p.Met1Val)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002796295]	uncertain significance	14	75049655	75049655	Human	1	name
11348637	CV241888	single nucleotide variant	NM_001040108.2(MLH3):c.8A>G (p.Lys3Arg)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000290922]\|Endometrial carcinoma [RCV005235154]\|Endometrial carcinoma [RCV005396759]\|not provided [RCV001573731]\|not specified [RCV000583075]	benign\|likely benign	14	75049648	75049648	Human	4	name
329363720	CV2422474	single nucleotide variant	NM_001040108.2(MLH3):c.54C>T (p.Ala18=)	not specified [RCV004244653]	likely benign	14	75049602	75049602	Human		name
329390053	CV2465735	single nucleotide variant	NM_001040108.2(MLH3):c.90C>G (p.Ala30=)	not specified [RCV004283391]	likely benign	14	75049566	75049566	Human		name
405702923	CV3388926	single nucleotide variant	NM_001040108.2(MLH3):c.63C>T (p.Ser21=)	not specified [RCV004521263]	likely benign	14	75049593	75049593	Human		name
407486984	CV3457376	single nucleotide variant	NM_001040108.2(MLH3):c.72A>G (p.Gln24=)	not specified [RCV004640978]	likely benign	14	75049584	75049584	Human		name
597960008	CV3815469	single nucleotide variant	NM_001040108.2(MLH3):c.4A>T (p.Ile2Phe)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005163403]	uncertain significance	14	75049652	75049652	Human	1	name
15133720	CV769918	single nucleotide variant	NM_001040108.2(MLH3):c.39G>A (p.Leu13=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001392277]\|not specified [RCV004029727]	likely benign	14	75049617	75049617	Human	1	name
26889539	CV841775	single nucleotide variant	NM_001040108.2(MLH3):c.6C>G (p.Ile2Met)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001058280]\|Endometrial carcinoma [RCV005005016]\|not specified [RCV003321792]	uncertain significance	14	75049650	75049650	Human	4	name
38480857	CV936729	single nucleotide variant	NM_001040108.2(MLH3):c.3G>A (p.Met1Ile)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001206491]	uncertain significance	14	75049653	75049653	Human	1	name
127259118	CV1080728	single nucleotide variant	NM_001040108.2(MLH3):c.219T>C (p.Tyr73=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001419701]\|not specified [RCV004038170]	likely benign	14	75049437	75049437	Human	1	name
127297903	CV1123976	single nucleotide variant	NM_001040108.2(MLH3):c.147C>T (p.Thr49=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001460378]\|not specified [RCV004038585]	likely benign	14	75049509	75049509	Human	1	name
152050243	CV1533041	single nucleotide variant	NM_001040108.2(MLH3):c.240G>A (p.Ser80=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002166783]\|not specified [RCV004044968]	likely benign	14	75049416	75049416	Human	1	name
152127909	CV1572160	deletion	NM_001040108.2(MLH3):c.3643+6_3643+12del	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002217661]	likely benign	14	75038328	75038334	Human	1	name
152073151	CV1657406	single nucleotide variant	NM_001040108.2(MLH3):c.126T>G (p.Ala42=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002210247]\|MLH3-related disorder [RCV003893200]\|not specified [RCV004045633]	likely benign	14	75049530	75049530	Human	1	name , alternate_id
155671349	CV1829216	single nucleotide variant	NM_001040108.2(MLH3):c.132G>A (p.Arg44=)	not specified [RCV004058423]	likely benign	14	75049524	75049524	Human		name
155722305	CV1831321	single nucleotide variant	NM_001040108.2(MLH3):c.171T>C (p.Asn57=)	not specified [RCV004060617]	likely benign	14	75049485	75049485	Human		name
155738010	CV1831853	single nucleotide variant	NM_001040108.2(MLH3):c.180G>A (p.Gly60=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003505267]\|not specified [RCV004059317]	likely benign	14	75049476	75049476	Human	1	name
155720156	CV1835739	single nucleotide variant	NM_001040108.2(MLH3):c.129C>A (p.Val43=)	not specified [RCV004058235]	likely benign	14	75049527	75049527	Human		name
155733516	CV1842639	single nucleotide variant	NM_001040108.2(MLH3):c.189T>C (p.Ser63=)	not specified [RCV004060757]	likely benign	14	75049467	75049467	Human		name
155676076	CV1843355	single nucleotide variant	NM_001040108.2(MLH3):c.195T>C (p.Asp65=)	not specified [RCV004061536]	likely benign	14	75049461	75049461	Human		name
155671177	CV1843667	single nucleotide variant	NM_001040108.2(MLH3):c.204A>G (p.Lys68=)	not specified [RCV004059633]	likely benign	14	75049452	75049452	Human		name
155695470	CV1844634	single nucleotide variant	NM_001040108.2(MLH3):c.225C>G (p.Thr75=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005098034]\|not specified [RCV004061942]	likely benign	14	75049431	75049431	Human	1	name
155695490	CV1844640	single nucleotide variant	NM_001040108.2(MLH3):c.225C>T (p.Thr75=)	not specified [RCV004061943]	likely benign	14	75049431	75049431	Human		name
155671560	CV1845633	single nucleotide variant	NM_001040108.2(MLH3):c.258T>C (p.Asn86=)	not specified [RCV004062849]	likely benign	14	75049398	75049398	Human		name
155694474	CV1848101	single nucleotide variant	NM_001040108.2(MLH3):c.243A>G (p.Val81=)	not specified [RCV004063814]	likely benign	14	75049413	75049413	Human		name
155671538	CV1848591	single nucleotide variant	NM_001040108.2(MLH3):c.255G>A (p.Glu85=)	not specified [RCV004062221]	likely benign	14	75049401	75049401	Human		name
155683895	CV1849479	single nucleotide variant	NM_001040108.2(MLH3):c.198A>G (p.Val66=)	not specified [RCV004061669]	likely benign	14	75049458	75049458	Human		name
155685352	CV1850147	single nucleotide variant	NM_001040108.2(MLH3):c.20T>A (p.Val7Asp)	not specified [RCV004060321]	uncertain significance	14	75049636	75049636	Human		name
155706488	CV1850939	single nucleotide variant	NM_001040108.2(MLH3):c.22G>C (p.Glu8Gln)	not specified [RCV004062615]	uncertain significance	14	75049634	75049634	Human		name
155680000	CV1853141	single nucleotide variant	NM_001040108.2(MLH3):c.276C>T (p.Phe92=)	not specified [RCV004064175]	likely benign	14	75049380	75049380	Human		name
155687427	CV1853630	single nucleotide variant	NM_001040108.2(MLH3):c.294A>G (p.Ala98=)	not specified [RCV004065320]	likely benign	14	75049362	75049362	Human		name
155689789	CV1856532	single nucleotide variant	NM_001040108.2(MLH3):c.297T>C (p.Asn99=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005098367]\|not specified [RCV004065422]	likely benign	14	75049359	75049359	Human	1	name
11351311	CV241876	duplication	NM_001040108.2(MLH3):c.4243-37_4243-1dup	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000226357]\|not specified [RCV003321559]	benign\|uncertain significance	14	75017201	75017202	Human	1	name
329364660	CV2425892	single nucleotide variant	NM_001040108.2(MLH3):c.20T>C (p.Val7Ala)	not specified [RCV004243261]	uncertain significance	14	75049636	75049636	Human		name
329363699	CV2425923	single nucleotide variant	NM_001040108.2(MLH3):c.273T>A (p.Gly91=)	not specified [RCV004243292]	likely benign	14	75049383	75049383	Human		name
401776109	CV2724583	single nucleotide variant	NM_001040108.2(MLH3):c.123G>T (p.Val41=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003777165]\|not specified [RCV004331383]	likely benign	14	75049533	75049533	Human	1	name
401776179	CV2724607	single nucleotide variant	NM_001040108.2(MLH3):c.10T>G (p.Cys4Gly)	not specified [RCV004331407]	uncertain significance	14	75049646	75049646	Human		name
401776275	CV2724641	single nucleotide variant	NM_001040108.2(MLH3):c.135G>C (p.Val45=)	not specified [RCV004331441]	likely benign	14	75049521	75049521	Human		name
11634531	CV321382	indel	NM_001040108.2(MLH3):c.957_958delinsAT	Lynch syndrome [RCV000378224]	uncertain significance	14	75016124	75016125	Human		name
405701783	CV3392225	single nucleotide variant	NM_001040108.2(MLH3):c.10T>C (p.Cys4Arg)	not specified [RCV004521104]	uncertain significance	14	75049646	75049646	Human		name
405701925	CV3392245	single nucleotide variant	NM_001040108.2(MLH3):c.147C>G (p.Thr49=)	not specified [RCV004521123]	likely benign	14	75049509	75049509	Human		name
405702050	CV3392264	single nucleotide variant	NM_001040108.2(MLH3):c.192T>C (p.Asp64=)	not specified [RCV004521140]	likely benign	14	75049464	75049464	Human		name
407487091	CV3457394	single nucleotide variant	NM_001040108.2(MLH3):c.186G>C (p.Gly62=)	not specified [RCV004640995]	likely benign	14	75049470	75049470	Human		name
407487144	CV3457405	single nucleotide variant	NM_001040108.2(MLH3):c.210A>G (p.Gly70=)	not specified [RCV004641003]	likely benign	14	75049446	75049446	Human		name
597640903	CV3556968	single nucleotide variant	NM_001040108.2(MLH3):c.207G>A (p.Val69=)	not specified [RCV004825365]	likely benign	14	75049449	75049449	Human		name
597636323	CV3556972	single nucleotide variant	NM_001040108.2(MLH3):c.282A>C (p.Gly94=)	not specified [RCV004824513]	likely benign	14	75049374	75049374	Human		name
597636439	CV3557060	single nucleotide variant	NM_001040108.2(MLH3):c.250T>C (p.Leu84=)	not specified [RCV004824535]	likely benign	14	75049406	75049406	Human		name
597641517	CV3557148	single nucleotide variant	NM_001040108.2(MLH3):c.240G>T (p.Ser80=)	not specified [RCV004825473]	likely benign	14	75049416	75049416	Human		name
597676750	CV3710984	single nucleotide variant	NM_001040108.2(MLH3):c.13T>G (p.Leu5Val)	Endometrial carcinoma [RCV005005706]\|not specified [RCV005377683]	uncertain significance	14	75049643	75049643	Human	2	name
598166570	CV3989357	single nucleotide variant	NM_001040108.2(MLH3):c.231A>G (p.Lys77=)	not specified [RCV005369370]	likely benign	14	75049425	75049425	Human		name
598187893	CV3989408	single nucleotide variant	NM_001040108.2(MLH3):c.282A>G (p.Gly94=)	not specified [RCV005373634]	likely benign	14	75049374	75049374	Human		name
598187932	CV3989417	single nucleotide variant	NM_001040108.2(MLH3):c.240G>C (p.Ser80=)	not specified [RCV005373640]	likely benign	14	75049416	75049416	Human		name
12888065	CV400534	single nucleotide variant	NM_001040108.2(MLH3):c.162G>A (p.Val54=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000470225]\|not specified [RCV004023057]	likely benign	14	75049494	75049494	Human	1	name
15187506	CV725815	single nucleotide variant	NM_001040108.2(MLH3):c.285G>A (p.Glu95=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001491417]\|not specified [RCV004028360]	likely benign	14	75049371	75049371	Human	1	name
15112789	CV784790	single nucleotide variant	NM_001040108.2(MLH3):c.246G>A (p.Gln82=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001395009]\|not specified [RCV004030004]	likely benign	14	75049410	75049410	Human	1	name
126764928	CV1031720	single nucleotide variant	NM_001040108.2(MLH3):c.76G>T (p.Val26Phe)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001341838]\|not specified [RCV004035974]	uncertain significance	14	75049580	75049580	Human	1	name
126745712	CV1031721	single nucleotide variant	NM_001040108.2(MLH3):c.34A>G (p.Lys12Glu)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001337238]	uncertain significance	14	75049622	75049622	Human	1	name
127265782	CV1080727	single nucleotide variant	NM_001040108.2(MLH3):c.825A>G (p.Glu275=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001403652]\|not specified [RCV004037989]	likely benign	14	75048831	75048831	Human	1	name
127249439	CV1102554	single nucleotide variant	NM_001040108.2(MLH3):c.618C>T (p.Asp206=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001425120]\|not specified [RCV004038228]	likely benign	14	75049038	75049038	Human	1	name
127269830	CV1102555	single nucleotide variant	NM_001040108.2(MLH3):c.565T>C (p.Leu189=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001441208]\|not specified [RCV004038390]	likely benign	14	75049091	75049091	Human	1	name
127335217	CV1123973	single nucleotide variant	NM_001040108.2(MLH3):c.948G>A (p.Glu316=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001474095]\|not specified [RCV004037146]	likely benign	14	75048708	75048708	Human	1	name
127291219	CV1123974	single nucleotide variant	NM_001040108.2(MLH3):c.858C>A (p.Thr286=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001475999]\|not specified [RCV004037166]	likely benign	14	75048798	75048798	Human	1	name
127299392	CV1123975	single nucleotide variant	NM_001040108.2(MLH3):c.729A>G (p.Ala243=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001460794]\|not specified [RCV004038593]	likely benign	14	75048927	75048927	Human	1	name
127294784	CV1144840	single nucleotide variant	NM_001040108.2(MLH3):c.816A>G (p.Leu272=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001497068]\|not specified [RCV004037373]	likely benign	14	75048840	75048840	Human	1	name
127305976	CV1144841	single nucleotide variant	NM_001040108.2(MLH3):c.807C>T (p.Asp269=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001500067]\|not specified [RCV004037406]	likely benign	14	75048849	75048849	Human	1	name
127334049	CV1144842	single nucleotide variant	NM_001040108.2(MLH3):c.531T>C (p.Ala177=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001490576]\|not specified [RCV004037307]	likely benign	14	75049125	75049125	Human	1	name
127331555	CV1144843	single nucleotide variant	NM_001040108.2(MLH3):c.510G>A (p.Lys170=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001488886]\|not specified [RCV004037293]	likely benign	14	75049146	75049146	Human	1	name
151890662	CV1405279	single nucleotide variant	NM_001040108.2(MLH3):c.31G>A (p.Ala11Thr)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001888471]\|not specified [RCV004041097]	uncertain significance	14	75049625	75049625	Human	1	name
151846245	CV1434609	single nucleotide variant	NM_001040108.2(MLH3):c.82G>T (p.Glu28Ter)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001922153]\|not specified [RCV004041257]	uncertain significance	14	75049574	75049574	Human	1	name
151768256	CV1445412	single nucleotide variant	NM_001040108.2(MLH3):c.97A>G (p.Ser33Gly)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002025108]	uncertain significance	14	75049559	75049559	Human	1	name
151777948	CV1472317	single nucleotide variant	NM_001040108.2(MLH3):c.98G>A (p.Ser33Asn)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002045866]\|not specified [RCV004046770]	uncertain significance	14	75049558	75049558	Human	1	name
151748040	CV1478750	single nucleotide variant	NM_001040108.2(MLH3):c.71A>G (p.Gln24Arg)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002023062]\|not specified [RCV004641888]	uncertain significance	14	75049585	75049585	Human	1	name
151840398	CV1508197	single nucleotide variant	NM_001040108.2(MLH3):c.585T>G (p.Gly195=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001956677]\|not specified [RCV004044499]	likely benign	14	75049071	75049071	Human	1	name
152053730	CV1573315	single nucleotide variant	NM_001040108.2(MLH3):c.441A>G (p.Thr147=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002207830]\|not specified [RCV004045676]	likely benign	14	75049215	75049215	Human	1	name
152043256	CV1619810	single nucleotide variant	NM_001040108.2(MLH3):c.540C>T (p.Leu180=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002188535]	likely benign	14	75049116	75049116	Human	1	name
152169139	CV1636917	single nucleotide variant	NM_001040108.2(MLH3):c.744T>C (p.Asn248=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002182690]\|not specified [RCV004045064]	likely benign	14	75048912	75048912	Human	1	name
152088593	CV1638936	single nucleotide variant	NM_001040108.2(MLH3):c.564T>G (p.Ser188=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002150287]\|not specified [RCV004641925]	likely benign	14	75049092	75049092	Human	1	name
152107997	CV1643408	single nucleotide variant	NM_001040108.2(MLH3):c.774A>G (p.Leu258=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002096449]\|MLH3-related disorder [RCV003968896]\|not specified [RCV004045867]	likely benign	14	75048882	75048882	Human	1	name , alternate_id
155716037	CV1785076	single nucleotide variant	NM_001040108.2(MLH3):c.30A>C (p.Gln10His)	not specified [RCV004048328]	uncertain significance	14	75049626	75049626	Human		name
155709167	CV1785348	single nucleotide variant	NM_001040108.2(MLH3):c.321G>A (p.Val107=)	not specified [RCV004049009]	likely benign	14	75049335	75049335	Human		name
155664729	CV1787040	single nucleotide variant	NM_001040108.2(MLH3):c.388C>T (p.Leu130=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003505220]\|not specified [RCV004050338]	likely benign	14	75049268	75049268	Human	1	name
155704966	CV1787694	single nucleotide variant	NM_001040108.2(MLH3):c.40C>T (p.Arg14Cys)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005096482]\|not specified [RCV004051328]	uncertain significance	14	75049616	75049616	Human	1	name
155718933	CV1788719	single nucleotide variant	NM_001040108.2(MLH3):c.333C>G (p.Ser111=)	not specified [RCV004047770]	likely benign	14	75049323	75049323	Human		name
155686426	CV1789985	single nucleotide variant	NM_001040108.2(MLH3):c.384A>G (p.Lys128=)	not specified [RCV004048204]	likely benign	14	75049272	75049272	Human		name
155725780	CV1790980	single nucleotide variant	NM_001040108.2(MLH3):c.41G>C (p.Arg14Pro)	not specified [RCV004051875]	uncertain significance	14	75049615	75049615	Human		name
155717124	CV1792158	single nucleotide variant	NM_001040108.2(MLH3):c.32C>T (p.Ala11Val)	not specified [RCV004049496]	uncertain significance	14	75049624	75049624	Human		name
155677211	CV1792844	single nucleotide variant	NM_001040108.2(MLH3):c.360T>C (p.Phe120=)	not specified [RCV004049243]	likely benign	14	75049296	75049296	Human		name
155705598	CV1797231	single nucleotide variant	NM_001040108.2(MLH3):c.411G>A (p.Val137=)	not specified [RCV004051717]	likely benign	14	75049245	75049245	Human		name
155707522	CV1798675	single nucleotide variant	NM_001040108.2(MLH3):c.468T>A (p.Pro156=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005096632]\|not specified [RCV004051989]	likely benign	14	75049188	75049188	Human	1	name
155707529	CV1798676	single nucleotide variant	NM_001040108.2(MLH3):c.468T>C (p.Pro156=)	not specified [RCV004051990]	likely benign	14	75049188	75049188	Human		name
155739592	CV1799093	single nucleotide variant	NM_001040108.2(MLH3):c.492T>C (p.Pro164=)	not specified [RCV004050245]	likely benign	14	75049164	75049164	Human		name
155725626	CV1799577	single nucleotide variant	NM_001040108.2(MLH3):c.519G>A (p.Gln173=)	not specified [RCV004051677]	likely benign	14	75049137	75049137	Human		name
155669062	CV1800013	single nucleotide variant	NM_001040108.2(MLH3):c.546C>T (p.His182=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003096753]\|not specified [RCV004053113]	likely benign	14	75049110	75049110	Human	1	name
155746928	CV1800409	single nucleotide variant	NM_001040108.2(MLH3):c.573T>C (p.Asn191=)	not specified [RCV004053776]	likely benign	14	75049083	75049083	Human		name
155697387	CV1800945	single nucleotide variant	NM_001040108.2(MLH3):c.603C>G (p.Leu201=)	not specified [RCV004052615]	likely benign	14	75049053	75049053	Human		name
155697422	CV1800953	single nucleotide variant	NM_001040108.2(MLH3):c.603C>T (p.Leu201=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003505235]\|not specified [RCV004052617]	likely benign	14	75049053	75049053	Human	1	name
155735455	CV1801662	single nucleotide variant	NM_001040108.2(MLH3):c.462G>A (p.Gln154=)	not specified [RCV004051536]	likely benign	14	75049194	75049194	Human		name
155734262	CV1802246	single nucleotide variant	NM_001040108.2(MLH3):c.489C>T (p.Asp163=)	not specified [RCV004050176]	likely benign	14	75049167	75049167	Human		name
155722913	CV1802699	single nucleotide variant	NM_001040108.2(MLH3):c.514A>C (p.Arg172=)	not specified [RCV004051088]	likely benign	14	75049142	75049142	Human		name
155745245	CV1802731	single nucleotide variant	NM_001040108.2(MLH3):c.534C>G (p.Leu178=)	not specified [RCV004052436]	likely benign	14	75049122	75049122	Human		name
155744098	CV1803316	single nucleotide variant	NM_001040108.2(MLH3):c.564T>A (p.Ser188=)	not specified [RCV004053656]	likely benign	14	75049092	75049092	Human		name
155720448	CV1805391	single nucleotide variant	NM_001040108.2(MLH3):c.480A>G (p.Lys160=)	not specified [RCV004052165]	likely benign	14	75049176	75049176	Human		name
155743696	CV1806918	single nucleotide variant	NM_001040108.2(MLH3):c.561C>T (p.Phe187=)	not specified [RCV004053605]	likely benign	14	75049095	75049095	Human		name
155687074	CV1807352	single nucleotide variant	NM_001040108.2(MLH3):c.58A>G (p.Ser20Gly)	not specified [RCV004054239]	uncertain significance	14	75049598	75049598	Human		name
155705964	CV1807447	single nucleotide variant	NM_001040108.2(MLH3):c.612C>G (p.Thr204=)	not specified [RCV004053292]	likely benign	14	75049044	75049044	Human		name
155730649	CV1808475	single nucleotide variant	NM_001040108.2(MLH3):c.450C>T (p.Asn150=)	not specified [RCV004050825]	likely benign	14	75049206	75049206	Human		name
155731778	CV1808693	single nucleotide variant	NM_001040108.2(MLH3):c.453A>C (p.Leu151=)	not specified [RCV004051391]	likely benign	14	75049203	75049203	Human		name
155740125	CV1809235	single nucleotide variant	NM_001040108.2(MLH3):c.496C>T (p.Leu166=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003102665]\|MLH3-related disorder [RCV003961008]\|not specified [RCV004050306]	likely benign	14	75049160	75049160	Human	1	name , alternate_id
155740371	CV1809360	single nucleotide variant	NM_001040108.2(MLH3):c.498G>A (p.Leu166=)	not specified [RCV004050332]	likely benign	14	75049158	75049158	Human		name
155740382	CV1809367	single nucleotide variant	NM_001040108.2(MLH3):c.498G>T (p.Leu166=)	not specified [RCV004050334]	likely benign	14	75049158	75049158	Human		name
155704206	CV1810647	single nucleotide variant	NM_001040108.2(MLH3):c.57A>G (p.Ile19Met)	not specified [RCV004054108]	uncertain significance	14	75049599	75049599	Human		name
155705324	CV1811171	single nucleotide variant	NM_001040108.2(MLH3):c.609A>G (p.Lys203=)	not specified [RCV004052711]	likely benign	14	75049047	75049047	Human		name
155698041	CV1811875	single nucleotide variant	NM_001040108.2(MLH3):c.65T>C (p.Leu22Ser)	not specified [RCV004054450]	uncertain significance	14	75049591	75049591	Human		name
155716315	CV1812552	single nucleotide variant	NM_001040108.2(MLH3):c.696G>A (p.Glu232=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005097040]\|not specified [RCV004053524]	likely benign	14	75048960	75048960	Human	1	name
155697942	CV1813087	single nucleotide variant	NM_001040108.2(MLH3):c.754T>C (p.Leu252=)	not specified [RCV004056389]	likely benign	14	75048902	75048902	Human		name
155747329	CV1813566	single nucleotide variant	NM_001040108.2(MLH3):c.792A>G (p.Leu264=)	not specified [RCV004054783]	likely benign	14	75048864	75048864	Human		name
155665666	CV1813882	single nucleotide variant	NM_001040108.2(MLH3):c.79G>A (p.Glu27Lys)	not specified [RCV004055365]	uncertain significance	14	75049577	75049577	Human		name
155724879	CV1814735	single nucleotide variant	NM_001040108.2(MLH3):c.91C>G (p.Leu31Val)	not specified [RCV004055074]	uncertain significance	14	75049565	75049565	Human		name
155671117	CV1815588	single nucleotide variant	NM_001040108.2(MLH3):c.714T>C (p.Tyr238=)	not specified [RCV004055304]	likely benign	14	75048942	75048942	Human		name
155679983	CV1815841	single nucleotide variant	NM_001040108.2(MLH3):c.71A>T (p.Gln24Leu)	not specified [RCV004055746]	uncertain significance	14	75049585	75049585	Human		name
155747169	CV1816708	single nucleotide variant	NM_001040108.2(MLH3):c.789G>A (p.Lys263=)	not specified [RCV004054763]	likely benign	14	75048867	75048867	Human		name
155721600	CV1817306	single nucleotide variant	NM_001040108.2(MLH3):c.864G>A (p.Arg288=)	not specified [RCV004056592]	likely benign	14	75048792	75048792	Human		name
155710605	CV1817724	single nucleotide variant	NM_001040108.2(MLH3):c.909T>C (p.Tyr303=)	not specified [RCV004054989]	likely benign	14	75048747	75048747	Human		name
155693024	CV1818096	single nucleotide variant	NM_001040108.2(MLH3):c.957G>A (p.Val319=)	not specified [RCV004056933]	likely benign	14	75048699	75048699	Human		name
155668371	CV1818162	single nucleotide variant	NM_001040108.2(MLH3):c.95A>G (p.Asn32Ser)	not specified [RCV004056947]	uncertain significance	14	75049561	75049561	Human		name
155672675	CV1818476	single nucleotide variant	NM_001040108.2(MLH3):c.969A>G (p.Pro323=)	not specified [RCV004057017]	likely benign	14	75048687	75048687	Human		name
155670085	CV1819100	single nucleotide variant	NM_001040108.2(MLH3):c.708T>C (p.Ser236=)	not specified [RCV004055240]	likely benign	14	75048948	75048948	Human		name
155670398	CV1819170	single nucleotide variant	NM_001040108.2(MLH3):c.70C>T (p.Gln24Ter)	not specified [RCV004055256]	uncertain significance	14	75049586	75049586	Human		name
155670720	CV1819256	single nucleotide variant	NM_001040108.2(MLH3):c.711C>A (p.Gly237=)	not specified [RCV004055271]	likely benign	14	75048945	75048945	Human		name
155718341	CV1819354	single nucleotide variant	NM_001040108.2(MLH3):c.738C>T (p.Asn246=)	not specified [RCV004055969]	likely benign	14	75048918	75048918	Human		name
155697792	CV1820519	single nucleotide variant	NM_001040108.2(MLH3):c.819G>A (p.Arg273=)	not specified [RCV004055532]	likely benign	14	75048837	75048837	Human		name
155714768	CV1820863	single nucleotide variant	NM_001040108.2(MLH3):c.85C>G (p.Leu29Val)	not specified [RCV004056544]	uncertain significance	14	75049571	75049571	Human		name
155700240	CV1821041	single nucleotide variant	NM_001040108.2(MLH3):c.89C>T (p.Ala30Val)	not specified [RCV004054914]	uncertain significance	14	75049567	75049567	Human		name
155692433	CV1821594	single nucleotide variant	NM_001040108.2(MLH3):c.951T>C (p.Tyr317=)	not specified [RCV004056879]	likely benign	14	75048705	75048705	Human		name
155692816	CV1821694	single nucleotide variant	NM_001040108.2(MLH3):c.954T>C (p.Asp318=)	not specified [RCV004056904]	likely benign	14	75048702	75048702	Human		name
155726937	CV1822350	single nucleotide variant	NM_001040108.2(MLH3):c.699T>C (p.Phe233=)	not specified [RCV004055100]	likely benign	14	75048957	75048957	Human		name
155728873	CV1822689	single nucleotide variant	NM_001040108.2(MLH3):c.72A>C (p.Gln24His)	not specified [RCV004599323]	uncertain significance	14	75049584	75049584	Human		name
155708349	CV1823248	single nucleotide variant	NM_001040108.2(MLH3):c.765C>T (p.Asn255=)	not specified [RCV004056496]	likely benign	14	75048891	75048891	Human		name
155666299	CV1823616	single nucleotide variant	NM_001040108.2(MLH3):c.801C>A (p.Leu267=)	not specified [RCV004055382]	likely benign	14	75048855	75048855	Human		name
155742568	CV1823751	single nucleotide variant	NM_001040108.2(MLH3):c.804T>C (p.Ile268=)	not specified [RCV004055406]	likely benign	14	75048852	75048852	Human		name
155712028	CV1824218	single nucleotide variant	NM_001040108.2(MLH3):c.846G>A (p.Lys282=)	not specified [RCV004056167]	likely benign	14	75048810	75048810	Human		name
155698653	CV1824409	single nucleotide variant	NM_001040108.2(MLH3):c.885G>A (p.Arg295=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003103535]\|not specified [RCV004056766]	likely benign	14	75048771	75048771	Human	1	name
155723150	CV1824415	single nucleotide variant	NM_001040108.2(MLH3):c.885G>T (p.Arg295=)	not specified [RCV003321935]	likely benign	14	75048771	75048771	Human		name
155699328	CV1824610	single nucleotide variant	NM_001040108.2(MLH3):c.891G>C (p.Arg297=)	not specified [RCV004054866]	likely benign	14	75048765	75048765	Human		name
155673831	CV1825644	single nucleotide variant	NM_001040108.2(MLH3):c.978T>G (p.Thr326=)	not specified [RCV004057611]	likely benign	14	75048678	75048678	Human		name
155673893	CV1825659	single nucleotide variant	NM_001040108.2(MLH3):c.979C>T (p.Leu327=)	not specified [RCV004057615]	likely benign	14	75048677	75048677	Human		name
155703861	CV1828730	single nucleotide variant	NM_001040108.2(MLH3):c.981G>C (p.Leu327=)	not specified [RCV004057628]	likely benign	14	75048675	75048675	Human		name
155666841	CV1856768	single nucleotide variant	NM_001040108.2(MLH3):c.29A>G (p.Gln10Arg)	not specified [RCV004065477]	uncertain significance	14	75049627	75049627	Human		name
155799585	CV1859894	single nucleotide variant	NM_001040108.2(MLH3):c.367C>T (p.Leu123=)	not specified [RCV002466138]	likely benign	14	75049289	75049289	Human		name
155799588	CV1859895	deletion	NM_001040108.2(MLH3):c.124del (p.Ala42fs)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005051975]\|not provided [RCV002466139]	likely pathogenic	14	75049532	75049532	Human	1	name
155955971	CV1876755	single nucleotide variant	NM_001040108.2(MLH3):c.711C>T (p.Gly237=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003074414]\|not specified [RCV004827927]	likely benign	14	75048945	75048945	Human	1	name
156025525	CV1917562	single nucleotide variant	NM_001040108.2(MLH3):c.843A>G (p.Pro281=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002619611]\|not specified [RCV004069045]	likely benign	14	75048813	75048813	Human	1	name
8558782	CV20597	single nucleotide variant	NM_001040108.2(MLH3):c.70C>G (p.Gln24Glu)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000005897]\|not specified [RCV004018569]	uncertain significance	14	75049586	75049586	Human	1	name
156058435	CV2089967	single nucleotide variant	NM_001040108.2(MLH3):c.414T>G (p.Thr138=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002868024]	likely benign	14	75049242	75049242	Human	1	name
10767232	CV222390	single nucleotide variant	NM_001040108.2(MLH3):c.444G>C (p.Val148=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000331433]\|Endometrial carcinoma [RCV005235116]\|Endometrial carcinoma [RCV005396672]\|MLH3-related disorder [RCV003927885]\|not provided [RCV001711985]\|not specified [RCV000584205]	benign\|likely benign	14	75049212	75049212	Human	5	name , alternate_id
10768480	CV222391	single nucleotide variant	NM_001040108.2(MLH3):c.408T>C (p.Asp136=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000296304]\|Endometrial carcinoma [RCV005396671]\|not provided [RCV003390954]\|not specified [RCV000581807]	benign\|likely benign\|uncertain significance	14	75049248	75049248	Human	4	name
11347884	CV241883	single nucleotide variant	NM_001040108.2(MLH3):c.837C>T (p.Cys279=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000261305]\|Endometrial carcinoma [RCV005396758]\|not specified [RCV002465582]	benign\|likely benign\|uncertain significance	14	75048819	75048819	Human	4	name
11346652	CV241886	single nucleotide variant	NM_001040108.2(MLH3):c.429G>A (p.Gly143=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000388246]\|Endometrial carcinoma [RCV005396757]\|MLH3-related disorder [RCV003907857]\|not provided [RCV004703493]\|not specified [RCV004020772]	benign\|likely benign\|uncertain significance	14	75049227	75049227	Human	5	name , alternate_id
329364719	CV2422464	single nucleotide variant	NM_001040108.2(MLH3):c.435T>C (p.Thr145=)	not specified [RCV004243305]	likely benign	14	75049221	75049221	Human		name
329364727	CV2422469	single nucleotide variant	NM_001040108.2(MLH3):c.378T>C (p.Ser126=)	not specified [RCV004243310]	likely benign	14	75049278	75049278	Human		name
329364646	CV2425884	single nucleotide variant	NM_001040108.2(MLH3):c.44C>T (p.Ser15Phe)	not specified [RCV004243253]	uncertain significance	14	75049612	75049612	Human		name
329363708	CV2425932	single nucleotide variant	NM_001040108.2(MLH3):c.432T>C (p.Thr144=)	not specified [RCV004243301]	likely benign	14	75049224	75049224	Human		name
329390029	CV2465723	single nucleotide variant	NM_001040108.2(MLH3):c.47G>T (p.Gly16Val)	not specified [RCV004281542]	uncertain significance	14	75049609	75049609	Human		name
401776121	CV2724587	single nucleotide variant	NM_001040108.2(MLH3):c.828T>C (p.Ser276=)	not specified [RCV004331387]	likely benign	14	75048828	75048828	Human		name
401776256	CV2724634	single nucleotide variant	NM_001040108.2(MLH3):c.52G>T (p.Ala18Ser)	not specified [RCV004331434]	uncertain significance	14	75049604	75049604	Human		name
401798207	CV2741380	deletion	NM_001040108.2(MLH3):c.4090+39_4090+61del	not specified [RCV003322543]	likely benign	14	75022753	75022775	Human		name
401798220	CV2741388	single nucleotide variant	NM_001040108.2(MLH3):c.47G>A (p.Gly16Asp)	not specified [RCV003322551]	uncertain significance	14	75049609	75049609	Human		name
401895503	CV2784140	single nucleotide variant	NM_001040108.2(MLH3):c.795T>C (p.His265=)	not specified [RCV004366386]	likely benign	14	75048861	75048861	Human		name
401877929	CV2786866	single nucleotide variant	NM_001040108.2(MLH3):c.939A>G (p.Gln313=)	not specified [RCV004366018]	likely benign	14	75048717	75048717	Human		name
405108781	CV3046765	deletion	NM_001040108.2(MLH3):c.4091-13_4091-10del	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003615135]	likely benign	14	75018990	75018993	Human	1	name
405108763	CV3053631	single nucleotide variant	NM_001040108.2(MLH3):c.471A>C (p.Val157=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003615131]	likely benign	14	75049185	75049185	Human	1	name
405702833	CV3388913	single nucleotide variant	NM_001040108.2(MLH3):c.49T>G (p.Leu17Val)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005100767]\|not specified [RCV004521251]	uncertain significance	14	75049607	75049607	Human	1	name
405702843	CV3388914	single nucleotide variant	NM_001040108.2(MLH3):c.520A>C (p.Arg174=)	not specified [RCV004521252]	likely benign	14	75049136	75049136	Human		name
405702850	CV3388915	single nucleotide variant	NM_001040108.2(MLH3):c.540C>G (p.Leu180=)	not specified [RCV004521253]	likely benign	14	75049116	75049116	Human		name
405702861	CV3388917	single nucleotide variant	NM_001040108.2(MLH3):c.552C>T (p.Ser184=)	not specified [RCV004521255]	likely benign	14	75049104	75049104	Human		name
405702910	CV3388924	single nucleotide variant	NM_001040108.2(MLH3):c.621A>T (p.Val207=)	not specified [RCV004521261]	likely benign	14	75049035	75049035	Human		name
405702918	CV3388925	single nucleotide variant	NM_001040108.2(MLH3):c.62C>A (p.Ser21Tyr)	not specified [RCV004521262]	uncertain significance	14	75049594	75049594	Human		name
405702982	CV3388934	single nucleotide variant	NM_001040108.2(MLH3):c.813A>G (p.Leu271=)	not specified [RCV004521271]	likely benign	14	75048843	75048843	Human		name
405702998	CV3388936	single nucleotide variant	NM_001040108.2(MLH3):c.83A>T (p.Glu28Val)	not specified [RCV004521273]	uncertain significance	14	75049573	75049573	Human		name
405703018	CV3388939	single nucleotide variant	NM_001040108.2(MLH3):c.91C>T (p.Leu31Phe)	not specified [RCV004521276]	uncertain significance	14	75049565	75049565	Human		name
405703025	CV3388940	single nucleotide variant	NM_001040108.2(MLH3):c.933G>A (p.Gln311=)	not specified [RCV004521277]	likely benign	14	75048723	75048723	Human		name
405703032	CV3388941	single nucleotide variant	NM_001040108.2(MLH3):c.936C>T (p.Cys312=)	not specified [RCV004521278]	likely benign	14	75048720	75048720	Human		name
11634477	CV339225	single nucleotide variant	NM_001040108.2(MLH3):c.666G>A (p.Lys222=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000274051]\|Endometrial carcinoma [RCV005235258]\|Endometrial carcinoma [RCV005396950]\|not provided [RCV003736710]\|not specified [RCV000582984]	benign\|likely benign	14	75048990	75048990	Human	4	name
407489714	CV3415039	duplication	NM_001040108.2(MLH3):c.3465+36_3465+37dup	not specified [RCV004597374]	likely benign	14	75041577	75041578	Human		name
407486643	CV3457310	single nucleotide variant	NM_001040108.2(MLH3):c.918T>C (p.Tyr306=)	not specified [RCV004640926]	likely benign	14	75048738	75048738	Human		name
407486919	CV3457363	single nucleotide variant	NM_001040108.2(MLH3):c.615A>G (p.Lys205=)	not specified [RCV004640968]	likely benign	14	75049041	75049041	Human		name
407486946	CV3457370	single nucleotide variant	NM_001040108.2(MLH3):c.687A>G (p.Lys229=)	not specified [RCV004640972]	likely benign	14	75048969	75048969	Human		name
407487078	CV3457392	single nucleotide variant	NM_001040108.2(MLH3):c.348A>G (p.Thr116=)	not specified [RCV004640993]	likely benign	14	75049308	75049308	Human		name
597641084	CV3557032	single nucleotide variant	NM_001040108.2(MLH3):c.654A>G (p.Gly218=)	not specified [RCV004825397]	likely benign	14	75049002	75049002	Human		name
597641140	CV3557049	single nucleotide variant	NM_001040108.2(MLH3):c.927T>C (p.Asn309=)	not specified [RCV004825407]	likely benign	14	75048729	75048729	Human		name
597636476	CV3557081	single nucleotide variant	NM_001040108.2(MLH3):c.62C>T (p.Ser21Phe)	not specified [RCV004824542]	uncertain significance	14	75049594	75049594	Human		name
597641263	CV3557084	single nucleotide variant	NM_001040108.2(MLH3):c.507G>A (p.Glu169=)	not specified [RCV004825429]	likely benign	14	75049149	75049149	Human		name
597641544	CV3557157	single nucleotide variant	NM_001040108.2(MLH3):c.621A>G (p.Val207=)	not specified [RCV004825477]	likely benign	14	75049035	75049035	Human		name
597940124	CV3836612	single nucleotide variant	NM_001040108.2(MLH3):c.576T>C (p.Asp192=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005187633]	likely benign	14	75049080	75049080	Human	1	name
598187721	CV3989356	single nucleotide variant	NM_001040108.2(MLH3):c.645T>C (p.Tyr215=)	not specified [RCV005373607]	likely benign	14	75049011	75049011	Human		name
598187744	CV3989365	single nucleotide variant	NM_001040108.2(MLH3):c.86T>C (p.Leu29Pro)	not specified [RCV005373610]	uncertain significance	14	75049570	75049570	Human		name
598166684	CV3989387	single nucleotide variant	NM_001040108.2(MLH3):c.396T>C (p.Ala132=)	not specified [RCV005369385]	likely benign	14	75049260	75049260	Human		name
598187856	CV3989394	single nucleotide variant	NM_001040108.2(MLH3):c.492T>G (p.Pro164=)	not specified [RCV005373628]	likely benign	14	75049164	75049164	Human		name
598166794	CV3989414	single nucleotide variant	NM_001040108.2(MLH3):c.705T>A (p.Leu235=)	not specified [RCV005369398]	likely benign	14	75048951	75048951	Human		name
598166801	CV3989420	single nucleotide variant	NM_001040108.2(MLH3):c.981G>A (p.Leu327=)	not specified [RCV005369399]	likely benign	14	75048675	75048675	Human		name
598188067	CV3989451	single nucleotide variant	NM_001040108.2(MLH3):c.67G>C (p.Gly23Arg)	not specified [RCV005373661]	uncertain significance	14	75049589	75049589	Human		name
598188074	CV3989453	single nucleotide variant	NM_001040108.2(MLH3):c.978T>C (p.Thr326=)	not specified [RCV005373662]	likely benign	14	75048678	75048678	Human		name
12883183	CV399922	single nucleotide variant	NM_001040108.2(MLH3):c.330G>A (p.Ser110=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000461112]\|Endometrial carcinoma [RCV005398676]\|not specified [RCV003321627]	benign\|likely benign	14	75049326	75049326	Human	4	name
12880767	CV400277	single nucleotide variant	NM_001040108.2(MLH3):c.735C>T (p.Tyr245=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000456627]\|Endometrial carcinoma [RCV005235347]\|Endometrial carcinoma [RCV005398674]\|not specified [RCV003321626]	benign\|likely benign	14	75048921	75048921	Human	4	name
12885830	CV400293	single nucleotide variant	NM_001040108.2(MLH3):c.423C>T (p.Ser141=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001119974]\|Endometrial carcinoma [RCV005398675]\|not specified [RCV002268105]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75049233	75049233	Human	4	name
13626805	CV528300	single nucleotide variant	NM_001040108.2(MLH3):c.41G>A (p.Arg14His)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000655381]\|not specified [RCV002268239]	uncertain significance	14	75049615	75049615	Human	1	name
13626826	CV528758	single nucleotide variant	NM_001040108.2(MLH3):c.861T>C (p.Ser287=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000655402]\|MLH3-related disorder [RCV003918095]\|not specified [RCV004025970]	likely benign	14	75048795	75048795	Human	1	name , alternate_id
13626835	CV528842	single nucleotide variant	NM_001040108.2(MLH3):c.402A>G (p.Glu134=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000655412]	likely benign	14	75049254	75049254	Human	1	name
15115839	CV693598	single nucleotide variant	NM_001040108.2(MLH3):c.867A>G (p.Gln289=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001489595]\|Endometrial carcinoma [RCV005392491]\|not specified [RCV004027818]	likely benign	14	75048789	75048789	Human	4	name
15156611	CV739338	single nucleotide variant	NM_001040108.2(MLH3):c.849T>C (p.Asn283=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001408673]\|not specified [RCV004028526]	likely benign	14	75048807	75048807	Human	1	name
15137319	CV739339	single nucleotide variant	NM_001040108.2(MLH3):c.471A>G (p.Val157=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000898783]\|not specified [RCV004028486]	likely benign	14	75049185	75049185	Human	1	name
38477367	CV936727	single nucleotide variant	NM_001040108.2(MLH3):c.61T>C (p.Ser21Pro)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001205058]\|not specified [RCV004033637]	uncertain significance	14	75049595	75049595	Human	1	name
38475450	CV936728	single nucleotide variant	NM_001040108.2(MLH3):c.59G>A (p.Ser20Asn)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001204280]\|not specified [RCV004033609]	uncertain significance	14	75049597	75049597	Human	1	name
126759150	CV1011213	deletion	NM_001040108.2(MLH3):c.405del (p.Asp136fs)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001317981]\|not specified [RCV004034919]	uncertain significance	14	75049251	75049251	Human	1	name
127253585	CV1080724	single nucleotide variant	NM_001040108.2(MLH3):c.2391C>T (p.Arg797=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001418338]\|not specified [RCV004038155]	likely benign	14	75047265	75047265	Human	1	name
127266170	CV1080726	single nucleotide variant	NM_001040108.2(MLH3):c.1710A>G (p.Thr570=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001403797]\|not specified [RCV004037992]	likely benign	14	75047946	75047946	Human	1	name
127270028	CV1102551	single nucleotide variant	NM_001040108.2(MLH3):c.2031G>A (p.Thr677=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001430472]\|not specified [RCV004038288]	likely benign	14	75047625	75047625	Human	1	name
127269951	CV1102552	single nucleotide variant	NM_001040108.2(MLH3):c.1815C>T (p.Ser605=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001430415]\|not specified [RCV004038287]	likely benign	14	75047841	75047841	Human	1	name
127295076	CV1123966	single nucleotide variant	NM_001040108.2(MLH3):c.2331A>T (p.Gly777=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001452400]\|not specified [RCV004038507]	likely benign	14	75047325	75047325	Human	1	name
127333905	CV1123967	single nucleotide variant	NM_001040108.2(MLH3):c.2328T>C (p.Asn776=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001473223]\|MLH3-related disorder [RCV003921000]\|not specified [RCV004037137]	likely benign	14	75047328	75047328	Human	1	name , alternate_id
127310595	CV1123968	single nucleotide variant	NM_001040108.2(MLH3):c.1980C>T (p.Ser660=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001456650]\|not specified [RCV005369883]	likely benign	14	75047676	75047676	Human	1	name
127307379	CV1123969	single nucleotide variant	NM_001040108.2(MLH3):c.1926T>C (p.Phe642=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001463007]\|not specified [RCV004038617]	likely benign	14	75047730	75047730	Human	1	name
127337745	CV1123971	single nucleotide variant	NM_001040108.2(MLH3):c.1077T>C (p.Gly359=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001475834]	likely benign	14	75048579	75048579	Human	1	name
127302557	CV1123972	single nucleotide variant	NM_001040108.2(MLH3):c.1047G>A (p.Lys349=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001454470]	likely benign	14	75048609	75048609	Human	1	name
127331998	CV1144834	single nucleotide variant	NM_001040108.2(MLH3):c.2916G>A (p.Leu972=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001489193]\|not specified [RCV004037295]	likely benign	14	75046740	75046740	Human	1	name
127291191	CV1144835	single nucleotide variant	NM_001040108.2(MLH3):c.2604G>A (p.Lys868=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001496164]\|not specified [RCV004037360]	likely benign	14	75047052	75047052	Human	1	name
127319204	CV1144837	single nucleotide variant	NM_001040108.2(MLH3):c.1887T>C (p.Asn629=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001483769]\|not specified [RCV004037240]	likely benign	14	75047769	75047769	Human	1	name
127322423	CV1144838	single nucleotide variant	NM_001040108.2(MLH3):c.1788T>C (p.Phe596=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001505119]	likely benign	14	75047868	75047868	Human	1	name
127293419	CV1144839	single nucleotide variant	NM_001040108.2(MLH3):c.1569G>A (p.Gln523=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001496779]\|not specified [RCV004037369]	likely benign	14	75048087	75048087	Human	1	name
150481127	CV1222103	deletion	NM_001040108.2(MLH3):c.3280+99_3280+102del	not provided [RCV001616901]	benign	14	75046274	75046277	Human		name
151859608	CV1337338	single nucleotide variant	NM_001040108.2(MLH3):c.281G>A (p.Gly94Glu)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001923832]\|not specified [RCV004641801]	uncertain significance	14	75049375	75049375	Human	1	name
151736985	CV1391600	single nucleotide variant	NM_001040108.2(MLH3):c.2280A>G (p.Gln760=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002041823]\|not specified [RCV004038776]	likely benign\|uncertain significance	14	75047376	75047376	Human	1	name
151883769	CV1432236	single nucleotide variant	NM_001040108.2(MLH3):c.2253A>G (p.Leu751=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002000124]\|not specified [RCV004044354]	likely benign	14	75047403	75047403	Human	1	name
151769627	CV1451016	single nucleotide variant	NM_001040108.2(MLH3):c.121G>A (p.Val41Met)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001929389]\|MLH3-related disorder [RCV003416618]\|not specified [RCV004044319]	uncertain significance	14	75049535	75049535	Human	1	name , alternate_id
151815737	CV1485629	deletion	NM_001040108.2(MLH3):c.826del (p.Ser276fs)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002029404]	uncertain significance	14	75048830	75048830	Human	1	name
151783197	CV1491812	single nucleotide variant	NM_001040108.2(MLH3):c.1608C>A (p.Gly536=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002026461]\|not specified [RCV004046793]	likely benign	14	75048048	75048048	Human	1	name
151762095	CV1496539	single nucleotide variant	NM_001040108.2(MLH3):c.236A>T (p.His79Leu)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001895447]	uncertain significance	14	75049420	75049420	Human	1	name
151770095	CV1504183	single nucleotide variant	NM_001040108.2(MLH3):c.196G>A (p.Val66Ile)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002045164]\|not specified [RCV004046040]	uncertain significance	14	75049460	75049460	Human	1	name
152088138	CV1527283	single nucleotide variant	NM_001040108.2(MLH3):c.1392T>C (p.Ser464=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002093794]\|not specified [RCV004046436]	likely benign	14	75048264	75048264	Human	1	name
152051249	CV1527923	single nucleotide variant	NM_001040108.2(MLH3):c.1458A>G (p.Lys486=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002089187]	likely benign	14	75048198	75048198	Human	1	name
152044501	CV1534474	single nucleotide variant	NM_001040108.2(MLH3):c.1836A>G (p.Val612=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002088386]\|not specified [RCV004045765]	likely benign	14	75047820	75047820	Human	1	name
152067919	CV1547556	single nucleotide variant	NM_001040108.2(MLH3):c.1956T>C (p.Thr652=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002074700]	likely benign	14	75047700	75047700	Human	1	name
152108394	CV1547994	single nucleotide variant	NM_001040108.2(MLH3):c.1908A>G (p.Thr636=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002174017]	likely benign	14	75047748	75047748	Human	1	name
152071460	CV1549129	single nucleotide variant	NM_001040108.2(MLH3):c.2028A>G (p.Arg676=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002091644]\|not specified [RCV004046454]	likely benign	14	75047628	75047628	Human	1	name
152048417	CV1549799	single nucleotide variant	NM_001040108.2(MLH3):c.1281T>C (p.Asp427=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002166549]\|not specified [RCV004047049]	likely benign	14	75048375	75048375	Human	1	name
152088183	CV1562883	single nucleotide variant	NM_001040108.2(MLH3):c.1404A>G (p.Ser468=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002113702]\|not specified [RCV004046484]	likely benign	14	75048252	75048252	Human	1	name
152076643	CV1565934	single nucleotide variant	NM_001040108.2(MLH3):c.2643G>A (p.Lys881=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002075822]\|not specified [RCV004045758]	likely benign	14	75047013	75047013	Human	1	name
152174512	CV1591135	single nucleotide variant	NM_001040108.2(MLH3):c.1875T>C (p.His625=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002184535]\|not specified [RCV004047126]	likely benign	14	75047781	75047781	Human	1	name
152153112	CV1592692	single nucleotide variant	NM_001040108.2(MLH3):c.1155T>C (p.Asp385=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002202284]\|not specified [RCV004045559]	likely benign	14	75048501	75048501	Human	1	name
152081576	CV1607825	single nucleotide variant	NM_001040108.2(MLH3):c.2562G>A (p.Lys854=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002193087]\|not specified [RCV003493922]	likely benign	14	75047094	75047094	Human	1	name
152145213	CV1616470	single nucleotide variant	NM_001040108.2(MLH3):c.2481A>G (p.Ser827=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002120926]\|not specified [RCV004046512]	likely benign	14	75047175	75047175	Human	1	name
152042907	CV1624315	single nucleotide variant	NM_001040108.2(MLH3):c.1761T>C (p.Ser587=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002126317]\|not specified [RCV004046587]	likely benign	14	75047895	75047895	Human	1	name
152056747	CV1647294	single nucleotide variant	NM_001040108.2(MLH3):c.2139A>G (p.Thr713=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002208188]\|not specified [RCV004827878]	likely benign	14	75047517	75047517	Human	1	name
152148582	CV1650778	single nucleotide variant	NM_001040108.2(MLH3):c.1983T>G (p.Thr661=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002157815]\|not specified [RCV004046388]	likely benign	14	75047673	75047673	Human	1	name
152172673	CV1652631	single nucleotide variant	NM_001040108.2(MLH3):c.1107T>C (p.Asn369=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002143856]\|not specified [RCV004046992]	likely benign	14	75048549	75048549	Human	1	name
152049601	CV1656252	single nucleotide variant	NM_001040108.2(MLH3):c.2076A>C (p.Thr692=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002207350]	likely benign	14	75047580	75047580	Human	1	name
152056048	CV1662804	single nucleotide variant	NM_001040108.2(MLH3):c.1494A>G (p.Glu498=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002146241]	likely benign	14	75048162	75048162	Human	1	name
152100202	CV1664086	single nucleotide variant	NM_001040108.2(MLH3):c.1776A>G (p.Arg592=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002078887]	likely benign	14	75047880	75047880	Human	1	name
152054532	CV1665455	single nucleotide variant	NM_001040108.2(MLH3):c.2061T>C (p.Pro687=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002089545]\|not specified [RCV004044924]	likely benign	14	75047595	75047595	Human	1	name
153303023	CV1690076	insertion	NM_001040108.2(MLH3):c.3570+28_3570+29insT	not specified [RCV002268976]	benign	14	75039882	75039883	Human		name
153303031	CV1690082	single nucleotide variant	NM_001040108.2(MLH3):c.2523A>G (p.Gln841=)	not specified [RCV002268982]	likely benign	14	75047133	75047133	Human		name
153303032	CV1690083	single nucleotide variant	NM_001040108.2(MLH3):c.2004A>G (p.Gln668=)	not specified [RCV002268983]	likely benign	14	75047652	75047652	Human		name
153303033	CV1690084	single nucleotide variant	NM_001040108.2(MLH3):c.1479A>G (p.Glu493=)	not specified [RCV002268984]	likely benign	14	75048177	75048177	Human		name
155733694	CV1788064	single nucleotide variant	NM_001040108.2(MLH3):c.116A>G (p.Lys39Arg)	not specified [RCV004049840]	uncertain significance	14	75049540	75049540	Human		name
155725065	CV1790896	single nucleotide variant	NM_001040108.2(MLH3):c.1167T>C (p.Asn389=)	not specified [RCV004051862]	likely benign	14	75048489	75048489	Human		name
155695287	CV1793969	single nucleotide variant	NM_001040108.2(MLH3):c.1161G>A (p.Arg387=)	not specified [RCV004050585]	likely benign	14	75048495	75048495	Human		name
155666962	CV1803118	single nucleotide variant	NM_001040108.2(MLH3):c.1200C>T (p.Ser400=)	not specified [RCV004053036]	likely benign	14	75048456	75048456	Human		name
155731255	CV1808571	deletion	NM_001040108.2(MLH3):c.451del (p.Leu151fs)	not specified [RCV004050850]	uncertain significance	14	75049205	75049205	Human		name
155707493	CV1812435	single nucleotide variant	NM_001040108.2(MLH3):c.1233G>T (p.Val411=)	not specified [RCV004052983]	likely benign	14	75048423	75048423	Human		name
155697755	CV1813055	single nucleotide variant	NM_001040108.2(MLH3):c.1245T>C (p.Thr415=)	not specified [RCV004056381]	likely benign	14	75048411	75048411	Human		name
155701159	CV1818288	single nucleotide variant	NM_001040108.2(MLH3):c.127G>C (p.Val43Leu)	not specified [RCV004056974]	uncertain significance	14	75049529	75049529	Human		name
155730355	CV1819843	single nucleotide variant	NM_001040108.2(MLH3):c.124G>C (p.Ala42Pro)	not specified [RCV004054637]	uncertain significance	14	75049532	75049532	Human		name
155677643	CV1826197	single nucleotide variant	NM_001040108.2(MLH3):c.1347C>T (p.Gly449=)	not specified [RCV004058762]	likely benign	14	75048309	75048309	Human		name
155678064	CV1826302	single nucleotide variant	NM_001040108.2(MLH3):c.1350T>C (p.His450=)	not specified [RCV004058789]	likely benign	14	75048306	75048306	Human		name
155689057	CV1826635	single nucleotide variant	NM_001040108.2(MLH3):c.141G>A (p.Met47Ile)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003774321]\|not specified [RCV004057232]	uncertain significance	14	75049515	75049515	Human	1	name
155689952	CV1826759	single nucleotide variant	NM_001040108.2(MLH3):c.1425A>T (p.Thr475=)	not specified [RCV004057257]	likely benign	14	75048231	75048231	Human		name
155690710	CV1826882	single nucleotide variant	NM_001040108.2(MLH3):c.142G>A (p.Glu48Lys)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005058619]\|not specified [RCV004057794]	uncertain significance	14	75049514	75049514	Human	1	name
155691182	CV1826983	single nucleotide variant	NM_001040108.2(MLH3):c.1434A>G (p.Ala478=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003614148]\|not specified [RCV004057822]	likely benign	14	75048222	75048222	Human	1	name
155684790	CV1827120	single nucleotide variant	NM_001040108.2(MLH3):c.1500G>C (p.Pro500=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003095252]\|not specified [RCV004058545]	likely benign	14	75048156	75048156	Human	1	name
155684797	CV1827122	single nucleotide variant	NM_001040108.2(MLH3):c.1500G>T (p.Pro500=)	not specified [RCV004058546]	likely benign	14	75048156	75048156	Human		name
155684925	CV1827159	single nucleotide variant	NM_001040108.2(MLH3):c.1503T>C (p.Cys501=)	not specified [RCV004058554]	likely benign	14	75048153	75048153	Human		name
155692041	CV1827395	single nucleotide variant	NM_001040108.2(MLH3):c.1515A>G (p.Leu505=)	not specified [RCV004058618]	likely benign	14	75048141	75048141	Human		name
155718472	CV1827775	single nucleotide variant	NM_001040108.2(MLH3):c.1593T>C (p.Ser531=)	not specified [RCV004057377]	likely benign	14	75048063	75048063	Human		name
155704643	CV1828057	single nucleotide variant	NM_001040108.2(MLH3):c.1665A>G (p.Lys555=)	not specified [RCV004059793]	likely benign	14	75047991	75047991	Human		name
155730334	CV1828626	single nucleotide variant	NM_001040108.2(MLH3):c.1752A>G (p.Lys584=)	not specified [RCV004061296]	likely benign	14	75047904	75047904	Human		name
155701455	CV1828669	single nucleotide variant	NM_001040108.2(MLH3):c.1755A>G (p.Lys585=)	not specified [RCV004061309]	likely benign	14	75047901	75047901	Human		name
155676213	CV1829325	single nucleotide variant	NM_001040108.2(MLH3):c.1335A>G (p.Ser445=)	not specified [RCV004058702]	likely benign	14	75048321	75048321	Human		name
155683429	CV1830230	single nucleotide variant	NM_001040108.2(MLH3):c.1488T>C (p.Ser496=)	not specified [RCV004058482]	likely benign	14	75048168	75048168	Human		name
155683627	CV1830264	single nucleotide variant	NM_001040108.2(MLH3):c.148T>G (p.Phe50Val)	not specified [RCV004058493]	uncertain significance	14	75049508	75049508	Human		name
155718517	CV1830429	single nucleotide variant	NM_001040108.2(MLH3):c.155T>C (p.Val52Ala)	not specified [RCV004059119]	uncertain significance	14	75049501	75049501	Human		name
155718684	CV1830455	single nucleotide variant	NM_001040108.2(MLH3):c.1560G>A (p.Glu520=)	not specified [RCV004059128]	likely benign	14	75048096	75048096	Human		name
155719077	CV1830520	single nucleotide variant	NM_001040108.2(MLH3):c.1563T>C (p.Ser521=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003505261]\|not specified [RCV004059150]	likely benign	14	75048093	75048093	Human	1	name
155710874	CV1831136	single nucleotide variant	NM_001040108.2(MLH3):c.1650A>G (p.Gln550=)	not specified [RCV004059720]	likely benign	14	75048006	75048006	Human		name
155711564	CV1831254	single nucleotide variant	NM_001040108.2(MLH3):c.1656G>A (p.Lys552=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003505264]\|not specified [RCV004059745]	likely benign	14	75048000	75048000	Human	1	name
155722477	CV1831368	single nucleotide variant	NM_001040108.2(MLH3):c.1722A>G (p.Val574=)	not specified [RCV004060632]	likely benign	14	75047934	75047934	Human		name
155745665	CV1831495	single nucleotide variant	NM_001040108.2(MLH3):c.1728T>C (p.Ser576=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003614159]\|not specified [RCV004060667]	likely benign	14	75047928	75047928	Human	1	name
155723761	CV1831590	single nucleotide variant	NM_001040108.2(MLH3):c.1731T>C (p.Ala577=)	not specified [RCV004060689]	likely benign	14	75047925	75047925	Human		name
155729980	CV1831679	single nucleotide variant	NM_001040108.2(MLH3):c.1737A>G (p.Thr579=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003100809]\|not specified [RCV004060713]	likely benign	14	75047919	75047919	Human	1	name
155737914	CV1831771	single nucleotide variant	NM_001040108.2(MLH3):c.1806A>G (p.Lys602=)	not specified [RCV004059292]	likely benign	14	75047850	75047850	Human		name
155737948	CV1831800	single nucleotide variant	NM_001040108.2(MLH3):c.1807T>C (p.Leu603=)	not specified [RCV004059298]	likely benign	14	75047849	75047849	Human		name
155737964	CV1831814	single nucleotide variant	NM_001040108.2(MLH3):c.1809A>G (p.Leu603=)	MLH3-related disorder [RCV003896179]\|not specified [RCV004059304]	likely benign	14	75047847	75047847	Human		name , alternate_id
155738330	CV1832004	single nucleotide variant	NM_001040108.2(MLH3):c.1818T>G (p.Thr606=)	not specified [RCV004059362]	likely benign	14	75047838	75047838	Human		name
155738373	CV1832026	single nucleotide variant	NM_001040108.2(MLH3):c.181A>T (p.Met61Leu)	not specified [RCV004059370]	uncertain significance	14	75049475	75049475	Human		name
155738501	CV1832064	single nucleotide variant	NM_001040108.2(MLH3):c.1821C>T (p.Gly607=)	not specified [RCV004059380]	likely benign	14	75047835	75047835	Human		name
155670484	CV1832358	single nucleotide variant	NM_001040108.2(MLH3):c.131G>C (p.Arg44Thr)	not specified [RCV004058363]	uncertain significance	14	75049525	75049525	Human		name
155670582	CV1832381	single nucleotide variant	NM_001040108.2(MLH3):c.1320G>A (p.Leu440=)	not specified [RCV004058368]	likely benign	14	75048336	75048336	Human		name
155711942	CV1833251	single nucleotide variant	NM_001040108.2(MLH3):c.1470T>A (p.Ser490=)	not specified [RCV004058013]	likely benign	14	75048186	75048186	Human		name
155712331	CV1833295	single nucleotide variant	NM_001040108.2(MLH3):c.1473C>T (p.Phe491=)	not specified [RCV004058027]	likely benign	14	75048183	75048183	Human		name
155707879	CV1833497	single nucleotide variant	NM_001040108.2(MLH3):c.1545A>G (p.Pro515=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005058644]\|not specified [RCV004059030]	likely benign	14	75048111	75048111	Human	1	name
155732915	CV1834139	single nucleotide variant	NM_001040108.2(MLH3):c.1050A>G (p.Gln350=)	not specified [RCV004058086]	likely benign	14	75048606	75048606	Human		name
155720802	CV1834491	single nucleotide variant	NM_001040108.2(MLH3):c.170A>G (p.Asn57Ser)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003774469]\|not specified [RCV004060561]	uncertain significance	14	75049486	75049486	Human	1	name
155721392	CV1834567	single nucleotide variant	NM_001040108.2(MLH3):c.1713A>G (p.Leu571=)	not specified [RCV004060584]	likely benign	14	75047943	75047943	Human		name
155721915	CV1834648	single nucleotide variant	NM_001040108.2(MLH3):c.1719A>C (p.Gly573=)	not specified [RCV004060603]	likely benign	14	75047937	75047937	Human		name
155715231	CV1834998	single nucleotide variant	NM_001040108.2(MLH3):c.1798C>A (p.Arg600=)	not specified [RCV004059256]	likely benign	14	75047858	75047858	Human		name
155732834	CV1835465	single nucleotide variant	NM_001040108.2(MLH3):c.1890T>C (p.Tyr630=)	not specified [RCV004060203]	likely benign	14	75047766	75047766	Human		name
155722051	CV1836017	single nucleotide variant	NM_001040108.2(MLH3):c.1308T>C (p.Asn436=)	not specified [RCV004058296]	likely benign	14	75048348	75048348	Human		name
155733274	CV1836064	single nucleotide variant	NM_001040108.2(MLH3):c.1365G>A (p.Glu455=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003505255]\|not specified [RCV004058862]	likely benign	14	75048291	75048291	Human	1	name
155733394	CV1836101	single nucleotide variant	NM_001040108.2(MLH3):c.1368A>G (p.Pro456=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005097472]\|not specified [RCV004058870]	likely benign	14	75048288	75048288	Human	1	name
155722904	CV1836379	single nucleotide variant	NM_001040108.2(MLH3):c.137A>C (p.Asn46Thr)	not specified [RCV004058931]	uncertain significance	14	75049519	75049519	Human		name
155700948	CV1836834	single nucleotide variant	NM_001040108.2(MLH3):c.1452T>C (p.Asn484=)	not specified [RCV004057921]	likely benign	14	75048204	75048204	Human		name
155692393	CV1836890	single nucleotide variant	NM_001040108.2(MLH3):c.1518A>G (p.Glu506=)	not specified [RCV004058638]	likely benign	14	75048138	75048138	Human		name
155692481	CV1836908	single nucleotide variant	NM_001040108.2(MLH3):c.1041T>C (p.Phe347=)	not specified [RCV004058642]	likely benign	14	75048615	75048615	Human		name
155693328	CV1837061	single nucleotide variant	NM_001040108.2(MLH3):c.1525T>C (p.Leu509=)	not specified [RCV004058680]	likely benign	14	75048131	75048131	Human		name
155706384	CV1837151	single nucleotide variant	NM_001040108.2(MLH3):c.1530C>T (p.Ser510=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003774370]\|not specified [RCV004058959]	likely benign	14	75048126	75048126	Human	1	name
155706622	CV1837215	single nucleotide variant	NM_001040108.2(MLH3):c.1533T>C (p.Pro511=)	not specified [RCV004058975]	likely benign	14	75048123	75048123	Human		name
155702064	CV1837560	single nucleotide variant	NM_001040108.2(MLH3):c.1608C>T (p.Gly536=)	not specified [RCV004057457]	likely benign	14	75048048	75048048	Human		name
155723047	CV1837795	single nucleotide variant	NM_001040108.2(MLH3):c.167A>G (p.Asp56Gly)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003100787]\|not specified [RCV004059868]	uncertain significance	14	75049489	75049489	Human	1	name
155724652	CV1838110	single nucleotide variant	NM_001040108.2(MLH3):c.1693C>T (p.Leu565=)	not specified [RCV004059950]	likely benign	14	75047963	75047963	Human		name
155724955	CV1838152	single nucleotide variant	NM_001040108.2(MLH3):c.1695G>A (p.Leu565=)	not specified [RCV004059965]	likely benign	14	75047961	75047961	Human		name
155703408	CV1838446	single nucleotide variant	NM_001040108.2(MLH3):c.1770T>C (p.Cys590=)	not specified [RCV004061399]	likely benign	14	75047886	75047886	Human		name
155745820	CV1838842	single nucleotide variant	NM_001040108.2(MLH3):c.1860A>T (p.Ser620=)	not specified [RCV004060059]	likely benign	14	75047796	75047796	Human		name
155739009	CV1839195	single nucleotide variant	NM_001040108.2(MLH3):c.182T>C (p.Met61Thr)	not specified [RCV004059416]	uncertain significance	14	75049474	75049474	Human		name
155743123	CV1839273	single nucleotide variant	NM_001040108.2(MLH3):c.1833T>C (p.His611=)	not specified [RCV004059433]	likely benign	14	75047823	75047823	Human		name
155743743	CV1839536	single nucleotide variant	NM_001040108.2(MLH3):c.1848A>G (p.Glu616=)	not specified [RCV004060010]	likely benign	14	75047808	75047808	Human		name
155676437	CV1839558	single nucleotide variant	NM_001040108.2(MLH3):c.1962C>T (p.Asp654=)	not specified [RCV004061551]	likely benign	14	75047694	75047694	Human		name
155683008	CV1839884	single nucleotide variant	NM_001040108.2(MLH3):c.197T>C (p.Val66Ala)	not specified [RCV004061636]	uncertain significance	14	75049459	75049459	Human		name
155683426	CV1839944	single nucleotide variant	NM_001040108.2(MLH3):c.1983T>C (p.Thr661=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005097869]\|not specified [RCV004061651]	likely benign	14	75047673	75047673	Human	1	name
155677419	CV1840005	single nucleotide variant	NM_001040108.2(MLH3):c.205G>T (p.Val69Leu)	not specified [RCV004059679]	uncertain significance	14	75049451	75049451	Human		name
155678443	CV1840253	single nucleotide variant	NM_001040108.2(MLH3):c.2076A>G (p.Thr692=)	Endometrial carcinoma [RCV005397420]\|not specified [RCV004060238]	likely benign	14	75047580	75047580	Human	2	name
155720068	CV1840434	single nucleotide variant	NM_001040108.2(MLH3):c.2160T>C (p.Tyr720=)	MLH3-related disorder [RCV003971298]\|not specified [RCV004061073]	likely benign	14	75047496	75047496	Human		name , alternate_id
155721948	CV1840739	single nucleotide variant	NM_001040108.2(MLH3):c.2178T>C (p.Asp726=)	not specified [RCV004061136]	likely benign	14	75047478	75047478	Human		name
155696082	CV1840933	single nucleotide variant	NM_001040108.2(MLH3):c.2268G>A (p.Lys756=)	not specified [RCV004061976]	likely benign	14	75047388	75047388	Human		name
155705604	CV1841089	single nucleotide variant	NM_001040108.2(MLH3):c.2277G>A (p.Arg759=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003505274]\|not specified [RCV004062527]	likely benign	14	75047379	75047379	Human	1	name
155706162	CV1841271	single nucleotide variant	NM_001040108.2(MLH3):c.2289G>A (p.Lys763=)	not specified [RCV004062563]	likely benign	14	75047367	75047367	Human		name
155685906	CV1841313	single nucleotide variant	NM_001040108.2(MLH3):c.237C>G (p.His79Gln)	not specified [RCV004063351]	uncertain significance	14	75049419	75049419	Human		name
155710630	CV1841497	single nucleotide variant	NM_001040108.2(MLH3):c.2394A>G (p.Leu798=)	not specified [RCV004063385]	likely benign	14	75047262	75047262	Human		name
155692399	CV1841539	single nucleotide variant	NM_001040108.2(MLH3):c.2397G>A (p.Glu799=)	not specified [RCV004063397]	likely benign	14	75047259	75047259	Human		name
155726289	CV1841582	single nucleotide variant	NM_001040108.2(MLH3):c.239C>T (p.Ser80Leu)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003505278]\|Endometrial carcinoma [RCV005002837]\|not specified [RCV004063403]	uncertain significance	14	75049417	75049417	Human	4	name
155714548	CV1841896	single nucleotide variant	NM_001040108.2(MLH3):c.2505T>C (p.Asp835=)	not specified [RCV004062038]	likely benign	14	75047151	75047151	Human		name
155693684	CV1842244	single nucleotide variant	NM_001040108.2(MLH3):c.2622C>G (p.Ala874=)	not specified [RCV004062971]	likely benign	14	75047034	75047034	Human		name
155693997	CV1842304	single nucleotide variant	NM_001040108.2(MLH3):c.2629T>C (p.Leu877=)	not specified [RCV004062990]	likely benign	14	75047027	75047027	Human		name
155701132	CV1842334	single nucleotide variant	NM_001040108.2(MLH3):c.2631A>G (p.Leu877=)	not specified [RCV004062996]	likely benign	14	75047025	75047025	Human		name
155701668	CV1842473	single nucleotide variant	NM_001040108.2(MLH3):c.2640G>A (p.Leu880=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003102056]\|not specified [RCV004063508]	likely benign	14	75047016	75047016	Human	1	name
155734203	CV1842812	single nucleotide variant	NM_001040108.2(MLH3):c.1908A>C (p.Thr636=)	not specified [RCV004060803]	likely benign	14	75047748	75047748	Human		name
155744191	CV1842980	single nucleotide variant	NM_001040108.2(MLH3):c.193G>C (p.Asp65His)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003100948]\|not specified [RCV004060951]	uncertain significance	14	75049463	75049463	Human	1	name
155675742	CV1843306	single nucleotide variant	NM_001040108.2(MLH3):c.1959A>G (p.Pro653=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003100960]\|not specified [RCV004061523]	likely benign	14	75047697	75047697	Human	1	name
155675769	CV1843308	single nucleotide variant	NM_001040108.2(MLH3):c.1959A>T (p.Pro653=)	not specified [RCV004061524]	likely benign	14	75047697	75047697	Human		name
155670569	CV1843544	single nucleotide variant	NM_001040108.2(MLH3):c.2040T>C (p.Ser680=)	not specified [RCV004059603]	likely benign	14	75047616	75047616	Human		name
155677210	CV1843799	single nucleotide variant	NM_001040108.2(MLH3):c.2058A>G (p.Glu686=)	not specified [RCV004059663]	likely benign	14	75047598	75047598	Human		name
155718976	CV1844081	single nucleotide variant	NM_001040108.2(MLH3):c.214C>G (p.Arg72Gly)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003101086]\|not specified [RCV004599382]	uncertain significance	14	75049442	75049442	Human	1	name
155718991	CV1844083	single nucleotide variant	NM_001040108.2(MLH3):c.214C>T (p.Arg72Cys)	not specified [RCV004061027]	uncertain significance	14	75049442	75049442	Human		name
155719286	CV1844128	single nucleotide variant	NM_001040108.2(MLH3):c.2151C>T (p.Phe717=)	not specified [RCV004061034]	likely benign	14	75047505	75047505	Human		name
155719472	CV1844162	single nucleotide variant	NM_001040108.2(MLH3):c.2154C>G (p.Pro718=)	not specified [RCV004061045]	likely benign	14	75047502	75047502	Human		name
155719877	CV1844242	single nucleotide variant	NM_001040108.2(MLH3):c.215G>A (p.Arg72His)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003101096]\|not specified [RCV004061062]	uncertain significance	14	75049441	75049441	Human	1	name
155719906	CV1844249	single nucleotide variant	NM_001040108.2(MLH3):c.215G>T (p.Arg72Leu)	not specified [RCV004061064]	uncertain significance	14	75049441	75049441	Human		name
155671487	CV1844388	single nucleotide variant	NM_001040108.2(MLH3):c.2244T>C (p.Ser748=)	not specified [RCV004061895]	likely benign	14	75047412	75047412	Human		name
155716548	CV1844704	single nucleotide variant	NM_001040108.2(MLH3):c.2349T>C (p.Ser783=)	not specified [RCV004063237]	likely benign	14	75047307	75047307	Human		name
155717137	CV1844854	single nucleotide variant	NM_001040108.2(MLH3):c.2358T>C (p.Val786=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005058782]\|not specified [RCV004063282]	likely benign	14	75047298	75047298	Human	1	name
155717208	CV1844877	single nucleotide variant	NM_001040108.2(MLH3):c.1008C>A (p.Leu336=)	not specified [RCV004063288]	likely benign	14	75048648	75048648	Human		name
155685518	CV1844975	single nucleotide variant	NM_001040108.2(MLH3):c.2367C>T (p.Asp789=)	not specified [RCV004063305]	likely benign	14	75047289	75047289	Human		name
155685725	CV1845082	single nucleotide variant	NM_001040108.2(MLH3):c.2374C>T (p.Leu792=)	not specified [RCV004063333]	likely benign	14	75047282	75047282	Human		name
155685784	CV1845108	single nucleotide variant	NM_001040108.2(MLH3):c.2376G>A (p.Leu792=)	not specified [RCV004063340]	likely benign	14	75047280	75047280	Human		name
155678146	CV1845230	single nucleotide variant	NM_001040108.2(MLH3):c.2472C>T (p.Ile824=)	not specified [RCV004063934]	likely benign	14	75047184	75047184	Human		name
155692085	CV1845590	single nucleotide variant	NM_001040108.2(MLH3):c.2589T>G (p.Pro863=)	not specified [RCV004062840]	likely benign	14	75047067	75047067	Human		name
155669515	CV1845687	single nucleotide variant	NM_001040108.2(MLH3):c.2595C>T (p.Asp865=)	not specified [RCV004062864]	likely benign	14	75047061	75047061	Human		name
155693180	CV1845863	single nucleotide variant	NM_001040108.2(MLH3):c.2607A>G (p.Ser869=)	not specified [RCV004062912]	likely benign	14	75047049	75047049	Human		name
155671657	CV1845898	single nucleotide variant	NM_001040108.2(MLH3):c.260C>T (p.Pro87Leu)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003505279]\|not specified [RCV004062922]	uncertain significance	14	75049396	75049396	Human	1	name
155739760	CV1846081	single nucleotide variant	NM_001040108.2(MLH3):c.1923A>G (p.Thr641=)	not specified [RCV004060871]	likely benign	14	75047733	75047733	Human		name
155739773	CV1846086	single nucleotide variant	NM_001040108.2(MLH3):c.1923A>T (p.Thr641=)	not specified [RCV004060872]	likely benign	14	75047733	75047733	Human		name
155740394	CV1846305	single nucleotide variant	NM_001040108.2(MLH3):c.1935A>G (p.Arg645=)	not specified [RCV004060924]	likely benign	14	75047721	75047721	Human		name
155747923	CV1846404	single nucleotide variant	NM_001040108.2(MLH3):c.2007G>A (p.Leu669=)	not specified [RCV004059487]	likely benign	14	75047649	75047649	Human		name
155747990	CV1846463	single nucleotide variant	NM_001040108.2(MLH3):c.2010C>T (p.Pro670=)	not specified [RCV004059499]	likely benign	14	75047646	75047646	Human		name
155668768	CV1846652	single nucleotide variant	NM_001040108.2(MLH3):c.2022T>C (p.Asn674=)	not specified [RCV004059532]	likely benign	14	75047634	75047634	Human		name
155748253	CV1846941	single nucleotide variant	NM_001040108.2(MLH3):c.2118A>G (p.Thr706=)	not specified [RCV004060387]	likely benign	14	75047538	75047538	Human		name
155690762	CV1847217	single nucleotide variant	NM_001040108.2(MLH3):c.2211C>A (p.Ser737=)	not specified [RCV004061764]	likely benign	14	75047445	75047445	Human		name
155698774	CV1847362	single nucleotide variant	NM_001040108.2(MLH3):c.2220C>A (p.Ile740=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003614172]\|MLH3-related disorder [RCV003984259]\|not specified [RCV004061800]	likely benign	14	75047436	75047436	Human	1	name , alternate_id
155671374	CV1847363	single nucleotide variant	NM_001040108.2(MLH3):c.2220C>T (p.Ile740=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003614173]\|not specified [RCV004061801]	likely benign	14	75047436	75047436	Human	1	name
155699608	CV1847595	single nucleotide variant	NM_001040108.2(MLH3):c.2233C>T (p.Leu745=)	not specified [RCV004061847]	likely benign	14	75047423	75047423	Human		name
155699644	CV1847607	single nucleotide variant	NM_001040108.2(MLH3):c.2235A>C (p.Leu745=)	not specified [RCV004061851]	likely benign	14	75047421	75047421	Human		name
155671424	CV1847611	single nucleotide variant	NM_001040108.2(MLH3):c.2235A>G (p.Leu745=)	not specified [RCV004061854]	likely benign	14	75047421	75047421	Human		name
155685331	CV1847885	single nucleotide variant	NM_001040108.2(MLH3):c.2334C>G (p.Val778=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005098083]\|not specified [RCV004062719]	likely benign	14	75047322	75047322	Human	1	name
155716272	CV1847987	single nucleotide variant	NM_001040108.2(MLH3):c.2340C>T (p.Thr780=)	not specified [RCV004062741]	likely benign	14	75047316	75047316	Human		name
155727410	CV1848207	single nucleotide variant	NM_001040108.2(MLH3):c.2445T>C (p.Asp815=)	not specified [RCV004063841]	likely benign	14	75047211	75047211	Human		name
155727778	CV1848473	single nucleotide variant	NM_001040108.2(MLH3):c.2463A>G (p.Ala821=)	not specified [RCV004063904]	likely benign	14	75047193	75047193	Human		name
155678971	CV1848539	single nucleotide variant	NM_001040108.2(MLH3):c.2557C>T (p.Leu853=)	not specified [RCV004062207]	likely benign	14	75047099	75047099	Human		name
155678992	CV1848557	single nucleotide variant	NM_001040108.2(MLH3):c.2559G>A (p.Leu853=)	not specified [RCV004062213]	likely benign	14	75047097	75047097	Human		name
155704162	CV1848966	single nucleotide variant	NM_001040108.2(MLH3):c.2688T>C (p.Phe896=)	not specified [RCV004063652]	likely benign	14	75046968	75046968	Human		name
155672129	CV1849131	single nucleotide variant	NM_001040108.2(MLH3):c.2700A>C (p.Pro900=)	not specified [RCV004063687]	likely benign	14	75046956	75046956	Human		name
155715268	CV1849380	single nucleotide variant	NM_001040108.2(MLH3):c.271G>A (p.Gly91Ser)	not specified [RCV004064007]	uncertain significance	14	75049385	75049385	Human		name
155684185	CV1849541	single nucleotide variant	NM_001040108.2(MLH3):c.1992A>G (p.Lys664=)	not specified [RCV004061680]	likely benign	14	75047664	75047664	Human		name
155747684	CV1849695	single nucleotide variant	NM_001040108.2(MLH3):c.199G>A (p.Glu67Lys)	not specified [RCV004061719]	uncertain significance	14	75049457	75049457	Human		name
155685307	CV1850121	single nucleotide variant	NM_001040108.2(MLH3):c.209G>A (p.Gly70Glu)	not specified [RCV004060317]	uncertain significance	14	75049447	75049447	Human		name
155685402	CV1850171	single nucleotide variant	NM_001040108.2(MLH3):c.2100T>C (p.Gly700=)	not specified [RCV004060326]	likely benign	14	75047556	75047556	Human		name
155685675	CV1850277	single nucleotide variant	NM_001040108.2(MLH3):c.2109A>G (p.Lys703=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005097945]\|not specified [RCV004060349]	likely benign	14	75047547	75047547	Human	1	name
155688527	CV1850391	single nucleotide variant	NM_001040108.2(MLH3):c.2190A>G (p.Thr730=)	not specified [RCV004061176]	likely benign	14	75047466	75047466	Human		name
155690092	CV1850636	single nucleotide variant	NM_001040108.2(MLH3):c.2202T>C (p.Ile734=)	not specified [RCV004061739]	likely benign	14	75047454	75047454	Human		name
155690281	CV1850666	single nucleotide variant	NM_001040108.2(MLH3):c.2205T>G (p.Gly735=)	not specified [RCV004061751]	likely benign	14	75047451	75047451	Human		name
155706862	CV1851043	single nucleotide variant	NM_001040108.2(MLH3):c.2307T>C (p.Asp769=)	not specified [RCV003493954]	likely benign	14	75047349	75047349	Human		name
155707065	CV1851093	single nucleotide variant	NM_001040108.2(MLH3):c.2310A>G (p.Thr770=)	not specified [RCV004062648]	likely benign	14	75047346	75047346	Human		name
155727129	CV1851363	single nucleotide variant	NM_001040108.2(MLH3):c.241G>C (p.Val81Leu)	not specified [RCV004063479]	uncertain significance	14	75049415	75049415	Human		name
155727224	CV1851426	single nucleotide variant	NM_001040108.2(MLH3):c.2424T>C (p.Thr808=)	not specified [RCV004063750]	likely benign	14	75047232	75047232	Human		name
155694010	CV1851559	single nucleotide variant	NM_001040108.2(MLH3):c.2433T>C (p.His811=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003614176]\|not specified [RCV004063791]	likely benign	14	75047223	75047223	Human	1	name
155670356	CV1852065	single nucleotide variant	NM_001040108.2(MLH3):c.264G>T (p.Arg88Ser)	not specified [RCV004063534]	uncertain significance	14	75049392	75049392	Human		name
155670716	CV1852248	single nucleotide variant	NM_001040108.2(MLH3):c.2667A>G (p.Thr889=)	not specified [RCV004063578]	likely benign	14	75046989	75046989	Human		name
155671901	CV1852326	single nucleotide variant	NM_001040108.2(MLH3):c.2673G>A (p.Gly891=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003505280]\|MLH3-related disorder [RCV003896191]\|not specified [RCV004063598]	likely benign	14	75046983	75046983	Human	1	name , alternate_id
155703317	CV1852327	single nucleotide variant	NM_001040108.2(MLH3):c.2673G>T (p.Gly891=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003505281]\|not specified [RCV004063599]	likely benign	14	75046983	75046983	Human	1	name
155703683	CV1852385	single nucleotide variant	NM_001040108.2(MLH3):c.110A>G (p.Glu37Gly)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003102102]\|not specified [RCV004063618]	uncertain significance	14	75049546	75049546	Human	1	name
155686744	CV1852691	single nucleotide variant	NM_001040108.2(MLH3):c.2805C>T (p.Ile935=)	not specified [RCV004062278]	likely benign	14	75046851	75046851	Human		name
155663935	CV1852904	single nucleotide variant	NM_001040108.2(MLH3):c.2823C>T (p.Ala941=)	not specified [RCV004062326]	likely benign	14	75046833	75046833	Human		name
155670235	CV1852949	single nucleotide variant	NM_001040108.2(MLH3):c.2649C>T (p.Ser883=)	not specified [RCV003493957]	likely benign	14	75047007	75047007	Human		name
155679820	CV1853091	single nucleotide variant	NM_001040108.2(MLH3):c.2766A>G (p.Leu922=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005098277]\|not specified [RCV004064159]	likely benign	14	75046890	75046890	Human	1	name
155685901	CV1853302	single nucleotide variant	NM_001040108.2(MLH3):c.2781T>C (p.His927=)	not specified [RCV004064207]	likely benign	14	75046875	75046875	Human		name
155685989	CV1853326	single nucleotide variant	NM_001040108.2(MLH3):c.2784A>G (p.Glu928=)	MLH3-related disorder [RCV003916472]\|not specified [RCV004064212]	likely benign	14	75046872	75046872	Human		name , alternate_id
155683096	CV1853492	single nucleotide variant	NM_001040108.2(MLH3):c.2937T>C (p.Val979=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003102899]\|not specified [RCV004063198]	likely benign	14	75046719	75046719	Human	1	name
155688027	CV1853761	single nucleotide variant	NM_001040108.2(MLH3):c.295A>G (p.Asn99Asp)	not specified [RCV004065356]	uncertain significance	14	75049361	75049361	Human		name
155688363	CV1853817	single nucleotide variant	NM_001040108.2(MLH3):c.2964C>T (p.Ile988=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003614192]\|not specified [RCV004065373]	likely benign	14	75046692	75046692	Human	1	name
155672358	CV1853956	single nucleotide variant	NM_001040108.2(MLH3):c.2730G>A (p.Lys910=)	not specified [RCV004064031]	likely benign	14	75046926	75046926	Human		name
155679144	CV1854160	single nucleotide variant	NM_001040108.2(MLH3):c.2748A>G (p.Thr916=)	not specified [RCV004064096]	likely benign	14	75046908	75046908	Human		name
155679366	CV1854249	single nucleotide variant	NM_001040108.2(MLH3):c.1009T>C (p.Leu337=)	not specified [RCV004064117]	likely benign	14	75048647	75048647	Human		name
155679388	CV1854257	single nucleotide variant	NM_001040108.2(MLH3):c.2754T>C (p.Asp918=)	not specified [RCV004064121]	likely benign	14	75046902	75046902	Human		name
155681587	CV1854574	single nucleotide variant	NM_001040108.2(MLH3):c.2919C>T (p.Pro973=)	not specified [RCV004063151]	likely benign	14	75046737	75046737	Human		name
155664822	CV1855274	single nucleotide variant	NM_001040108.2(MLH3):c.283G>A (p.Glu95Lys)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005098309]\|Endometrial carcinoma [RCV005002839]\|not specified [RCV004062382]	uncertain significance	14	75049373	75049373	Human	4	name
155673123	CV1855586	single nucleotide variant	NM_001040108.2(MLH3):c.2868C>T (p.Asn956=)	not specified [RCV004062462]	likely benign	14	75046788	75046788	Human		name
155673315	CV1855615	single nucleotide variant	NM_001040108.2(MLH3):c.286G>A (p.Ala96Thr)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005098317]\|not specified [RCV004062469]	uncertain significance	14	75049370	75049370	Human	1	name
155673802	CV1855684	single nucleotide variant	NM_001040108.2(MLH3):c.2877A>G (p.Thr959=)	not specified [RCV004062496]	likely benign	14	75046779	75046779	Human		name
155674226	CV1855740	single nucleotide variant	NM_001040108.2(MLH3):c.2880A>G (p.Thr960=)	not specified [RCV004063025]	likely benign	14	75046776	75046776	Human		name
155688987	CV1856428	single nucleotide variant	NM_001040108.2(MLH3):c.2970C>G (p.Ala990=)	not specified [RCV004065402]	likely benign	14	75046686	75046686	Human		name
155689511	CV1856495	single nucleotide variant	NM_001040108.2(MLH3):c.2979A>G (p.Gln993=)	not specified [RCV004065410]	likely benign	14	75046677	75046677	Human		name
156394783	CV1876985	single nucleotide variant	NM_001040108.2(MLH3):c.1998T>C (p.Ser666=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003068466]\|not specified [RCV004070440]	likely benign	14	75047658	75047658	Human	1	name
156346272	CV1892859	single nucleotide variant	NM_001040108.2(MLH3):c.2403T>G (p.Ser801=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003090653]	likely benign	14	75047253	75047253	Human	1	name
156235751	CV2036505	single nucleotide variant	NM_001040108.2(MLH3):c.178G>A (p.Gly60Arg)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002805489]	uncertain significance	14	75049478	75049478	Human	1	name
8558787	CV20602	deletion	NM_001040108.2(MLH3):c.885del (p.His296fs)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000005903]\|Endometrial cancer [RCV000005904]\|not specified [RCV004018570]	pathogenic\|uncertain significance	14	75048771	75048771	Human	2	name
156151462	CV2101387	single nucleotide variant	NM_001040108.2(MLH3):c.2826A>G (p.Thr942=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002890666]\|not specified [RCV004827908]	likely benign	14	75046830	75046830	Human	1	name
11346235	CV241887	single nucleotide variant	NM_001040108.2(MLH3):c.124G>A (p.Ala42Thr)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001119976]\|not specified [RCV004020769]	uncertain significance	14	75049532	75049532	Human	1	name
329364749	CV2422482	single nucleotide variant	NM_001040108.2(MLH3):c.170A>C (p.Asn57Thr)	not specified [RCV004244661]	uncertain significance	14	75049486	75049486	Human		name
329363662	CV2425879	single nucleotide variant	NM_001040108.2(MLH3):c.1173G>A (p.Gln391=)	not specified [RCV004243248]	likely benign	14	75048483	75048483	Human		name
329364648	CV2425885	single nucleotide variant	NM_001040108.2(MLH3):c.1863T>G (p.Thr621=)	not specified [RCV004243254]	likely benign	14	75047793	75047793	Human		name
329364650	CV2425886	single nucleotide variant	NM_001040108.2(MLH3):c.2958T>A (p.Val986=)	not specified [RCV004243255]	likely benign	14	75046698	75046698	Human		name
329363672	CV2425901	single nucleotide variant	NM_001040108.2(MLH3):c.2487G>A (p.Lys829=)	not specified [RCV004243270]	likely benign	14	75047169	75047169	Human		name
329364681	CV2425905	single nucleotide variant	NM_001040108.2(MLH3):c.1266A>G (p.Thr422=)	not specified [RCV004243274]	likely benign	14	75048390	75048390	Human		name
329364693	CV2425915	single nucleotide variant	NM_001040108.2(MLH3):c.247G>T (p.Asp83Tyr)	not specified [RCV004243284]	uncertain significance	14	75049409	75049409	Human		name
329364695	CV2425916	single nucleotide variant	NM_001040108.2(MLH3):c.246G>T (p.Gln82His)	not specified [RCV004243285]	uncertain significance	14	75049410	75049410	Human		name
329364701	CV2425921	single nucleotide variant	NM_001040108.2(MLH3):c.169A>G (p.Asn57Asp)	not specified [RCV004243290]	uncertain significance	14	75049487	75049487	Human		name
329364713	CV2425930	single nucleotide variant	NM_001040108.2(MLH3):c.2616A>G (p.Ser872=)	not specified [RCV004243299]	likely benign	14	75047040	75047040	Human		name
329390035	CV2465726	single nucleotide variant	NM_001040108.2(MLH3):c.202A>G (p.Lys68Glu)	not specified [RCV004281545]	uncertain significance	14	75049454	75049454	Human		name
329390041	CV2465729	single nucleotide variant	NM_001040108.2(MLH3):c.2448T>C (p.Ser816=)	not specified [RCV004281548]	likely benign	14	75047208	75047208	Human		name
329390046	CV2465731	single nucleotide variant	NM_001040108.2(MLH3):c.1311T>C (p.Asp437=)	not specified [RCV004283387]	likely benign	14	75048345	75048345	Human		name
329390063	CV2465740	single nucleotide variant	NM_001040108.2(MLH3):c.166G>A (p.Asp56Asn)	not specified [RCV004283396]	uncertain significance	14	75049490	75049490	Human		name
329390081	CV2465749	single nucleotide variant	NM_001040108.2(MLH3):c.139A>G (p.Met47Val)	not specified [RCV004283405]	uncertain significance	14	75049517	75049517	Human		name
329390090	CV2465754	single nucleotide variant	NM_001040108.2(MLH3):c.130A>G (p.Arg44Gly)	not specified [RCV004283410]	uncertain significance	14	75049526	75049526	Human		name
329390100	CV2465759	single nucleotide variant	NM_001040108.2(MLH3):c.2811A>G (p.Thr937=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005101378]\|not provided [RCV003395725]\|not specified [RCV004283415]	likely benign	14	75046845	75046845	Human	1	name
401775289	CV2724047	single nucleotide variant	NM_001040108.2(MLH3):c.245A>G (p.Gln82Arg)	not specified [RCV004326191]	uncertain significance	14	75049411	75049411	Human		name
401776112	CV2724584	single nucleotide variant	NM_001040108.2(MLH3):c.2259T>G (p.Ser753=)	not specified [RCV004331384]	likely benign	14	75047397	75047397	Human		name
401776133	CV2724591	single nucleotide variant	NM_001040108.2(MLH3):c.2913A>G (p.Val971=)	not specified [RCV004331391]	likely benign	14	75046743	75046743	Human		name
401776157	CV2724599	single nucleotide variant	NM_001040108.2(MLH3):c.235C>G (p.His79Asp)	not specified [RCV004331399]	uncertain significance	14	75049421	75049421	Human		name
401776206	CV2724616	single nucleotide variant	NM_001040108.2(MLH3):c.2931T>C (p.Ser977=)	not specified [RCV004331416]	likely benign	14	75046725	75046725	Human		name
401776257	CV2724635	single nucleotide variant	NM_001040108.2(MLH3):c.1179A>C (p.Ala393=)	not specified [RCV004331435]	likely benign	14	75048477	75048477	Human		name
401795955	CV2740092	single nucleotide variant	NM_001040108.2(MLH3):c.154G>A (p.Val52Ile)	not specified [RCV003320327]	uncertain significance	14	75049502	75049502	Human		name
401855609	CV2753027	single nucleotide variant	NM_001040108.2(MLH3):c.132G>T (p.Arg44Ser)	Endometrial carcinoma [RCV003338082]	uncertain significance	14	75049524	75049524	Human	2	name
401868918	CV2784105	single nucleotide variant	NM_001040108.2(MLH3):c.1113T>C (p.Phe371=)	not specified [RCV004366351]	likely benign	14	75048543	75048543	Human		name
401868928	CV2784108	single nucleotide variant	NM_001040108.2(MLH3):c.1362A>G (p.Thr454=)	not specified [RCV004366354]	likely benign	14	75048294	75048294	Human		name
401868930	CV2784109	single nucleotide variant	NM_001040108.2(MLH3):c.113C>A (p.Ala38Glu)	not specified [RCV004366355]	uncertain significance	14	75049543	75049543	Human		name
401895480	CV2784117	single nucleotide variant	NM_001040108.2(MLH3):c.2005T>C (p.Leu669=)	not specified [RCV004366363]	likely benign	14	75047651	75047651	Human		name
401895485	CV2784122	single nucleotide variant	NM_001040108.2(MLH3):c.1437A>G (p.Ser479=)	not specified [RCV004366368]	likely benign	14	75048219	75048219	Human		name
401895493	CV2784130	single nucleotide variant	NM_001040108.2(MLH3):c.160G>C (p.Val54Leu)	not specified [RCV004366376]	uncertain significance	14	75049496	75049496	Human		name
401895500	CV2784137	single nucleotide variant	NM_001040108.2(MLH3):c.2637A>G (p.Arg879=)	not specified [RCV004366383]	likely benign	14	75047019	75047019	Human		name
401895504	CV2784141	single nucleotide variant	NM_001040108.2(MLH3):c.2772C>T (p.Asn924=)	not specified [RCV004366387]	likely benign	14	75046884	75046884	Human		name
401895510	CV2784147	single nucleotide variant	NM_001040108.2(MLH3):c.2436T>C (p.Ser812=)	not specified [RCV004366393]	likely benign	14	75047220	75047220	Human		name
401897489	CV2787095	single nucleotide variant	NM_001040108.2(MLH3):c.146C>T (p.Thr49Ile)	not specified [RCV004366199]	uncertain significance	14	75049510	75049510	Human		name
402478770	CV2881435	single nucleotide variant	NM_001040108.2(MLH3):c.2646T>C (p.Gly882=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003506213]	likely benign	14	75047010	75047010	Human	1	name
402481020	CV2894003	single nucleotide variant	NM_001040108.2(MLH3):c.2778G>A (p.Lys926=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003506482]\|not specified [RCV004827977]	likely benign	14	75046878	75046878	Human	1	name
402472923	CV2931117	deletion	NM_001040108.2(MLH3):c.552del (p.Ile185fs)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003505013]	uncertain significance	14	75049104	75049104	Human	1	name
405106477	CV3008032	single nucleotide variant	NM_001040108.2(MLH3):c.260C>G (p.Pro87Arg)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003614610]	uncertain significance	14	75049396	75049396	Human	1	name
405109428	CV3060417	single nucleotide variant	NM_001040108.2(MLH3):c.242T>C (p.Val81Ala)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003615265]	uncertain significance	14	75049414	75049414	Human	1	name
405087985	CV3134066	single nucleotide variant	NM_001040108.2(MLH3):c.2415A>G (p.Lys805=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003834604]\|not specified [RCV004366882]	likely benign	14	75047241	75047241	Human	1	name
405252156	CV3177634	single nucleotide variant	NM_001040108.2(MLH3):c.2130A>G (p.Leu710=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003870592]	likely benign	14	75047526	75047526	Human	1	name
11634575	CV321393	single nucleotide variant	NM_001040108.2(MLH3):c.2373G>A (p.Leu791=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000393695]\|not specified [RCV004021616]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75047283	75047283	Human	1	name
11655446	CV337248	single nucleotide variant	NM_001040108.2(MLH3):c.206T>C (p.Val69Ala)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000325990]\|not specified [RCV004824053]	uncertain significance	14	75049450	75049450	Human	1	name
11634569	CV337250	single nucleotide variant	NM_001040108.2(MLH3):c.149T>A (p.Phe50Tyr)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000382973]\|Endometrial carcinoma [RCV001196283]\|Endometrial carcinoma [RCV005396951]\|Hereditary cancer [RCV000415369]\|not provided [RCV004791406]\|not specified [RCV002268024]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75049507	75049507	Human	5	name
11634579	CV339196	single nucleotide variant	NM_001040108.2(MLH3):c.2838C>A (p.Ser946=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000373022]\|not specified [RCV003493561]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75046818	75046818	Human	1	name
405701859	CV3392235	single nucleotide variant	NM_001040108.2(MLH3):c.1314A>G (p.Ala438=)	not specified [RCV004521114]	likely benign	14	75048342	75048342	Human		name
405701893	CV3392241	single nucleotide variant	NM_001040108.2(MLH3):c.1407G>A (p.Lys469=)	not specified [RCV004521119]	likely benign	14	75048249	75048249	Human		name
405701938	CV3392247	single nucleotide variant	NM_001040108.2(MLH3):c.150C>G (p.Phe50Leu)	not specified [RCV004521125]	uncertain significance	14	75049506	75049506	Human		name
405702013	CV3392257	single nucleotide variant	NM_001040108.2(MLH3):c.178G>T (p.Gly60Trp)	not specified [RCV004521135]	uncertain significance	14	75049478	75049478	Human		name
405702021	CV3392258	single nucleotide variant	NM_001040108.2(MLH3):c.1797G>A (p.Gly599=)	not specified [RCV004521136]	likely benign	14	75047859	75047859	Human		name
405702035	CV3392260	single nucleotide variant	NM_001040108.2(MLH3):c.183G>A (p.Met61Ile)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005100764]\|not specified [RCV004521138]	uncertain significance	14	75049473	75049473	Human	1	name
405702068	CV3392266	single nucleotide variant	NM_001040108.2(MLH3):c.195T>G (p.Asp65Glu)	not specified [RCV004521142]	uncertain significance	14	75049461	75049461	Human		name
405702145	CV3392277	single nucleotide variant	NM_001040108.2(MLH3):c.2260T>C (p.Leu754=)	not specified [RCV004521153]	likely benign	14	75047396	75047396	Human		name
405702152	CV3392278	single nucleotide variant	NM_001040108.2(MLH3):c.2265G>A (p.Glu755=)	not specified [RCV004521154]	likely benign	14	75047391	75047391	Human		name
405702196	CV3392284	single nucleotide variant	NM_001040108.2(MLH3):c.2382C>T (p.Asp794=)	not specified [RCV004521160]	likely benign	14	75047274	75047274	Human		name
405702205	CV3392285	single nucleotide variant	NM_001040108.2(MLH3):c.242T>A (p.Val81Glu)	not specified [RCV004521161]	uncertain significance	14	75049414	75049414	Human		name
405702235	CV3392289	single nucleotide variant	NM_001040108.2(MLH3):c.2535T>C (p.Ser845=)	not specified [RCV004521165]	likely benign	14	75047121	75047121	Human		name
405702255	CV3392292	single nucleotide variant	NM_001040108.2(MLH3):c.2565G>A (p.Glu855=)	not specified [RCV004521168]	likely benign	14	75047091	75047091	Human		name
405702269	CV3392294	single nucleotide variant	NM_001040108.2(MLH3):c.258T>G (p.Asn86Lys)	not specified [RCV004521170]	uncertain significance	14	75049398	75049398	Human		name
405702274	CV3392295	single nucleotide variant	NM_001040108.2(MLH3):c.2590T>C (p.Leu864=)	not specified [RCV004521171]	likely benign	14	75047066	75047066	Human		name
405702306	CV3392300	single nucleotide variant	NM_001040108.2(MLH3):c.2850T>C (p.Asn950=)	not specified [RCV004521175]	likely benign	14	75046806	75046806	Human		name
405702357	CV3392307	single nucleotide variant	NM_001040108.2(MLH3):c.2908T>C (p.Leu970=)	not specified [RCV004521182]	likely benign	14	75046748	75046748	Human		name
405702362	CV3392308	single nucleotide variant	NM_001040108.2(MLH3):c.2914T>C (p.Leu972=)	not specified [RCV004521183]	likely benign	14	75046742	75046742	Human		name
405702378	CV3392310	single nucleotide variant	NM_001040108.2(MLH3):c.2943T>C (p.Gly981=)	not specified [RCV004521185]	likely benign	14	75046713	75046713	Human		name
405702387	CV3392311	single nucleotide variant	NM_001040108.2(MLH3):c.2952A>G (p.Ser984=)	not specified [RCV004521186]	likely benign	14	75046704	75046704	Human		name
405702395	CV3392312	single nucleotide variant	NM_001040108.2(MLH3):c.2952A>T (p.Ser984=)	not specified [RCV004521187]	likely benign	14	75046704	75046704	Human		name
407489641	CV3415042	single nucleotide variant	NM_001040108.2(MLH3):c.1950T>C (p.Val650=)	not specified [RCV004597377]	likely benign	14	75047706	75047706	Human		name
407486729	CV3457325	single nucleotide variant	NM_001040108.2(MLH3):c.278G>C (p.Arg93Pro)	not specified [RCV004640938]	uncertain significance	14	75049378	75049378	Human		name
407486765	CV3457332	single nucleotide variant	NM_001040108.2(MLH3):c.1200C>A (p.Ser400=)	not specified [RCV004640943]	likely benign	14	75048456	75048456	Human		name
407486772	CV3457334	single nucleotide variant	NM_001040108.2(MLH3):c.1587A>G (p.Lys529=)	not specified [RCV004640944]	likely benign	14	75048069	75048069	Human		name
407486844	CV3457349	single nucleotide variant	NM_001040108.2(MLH3):c.2184G>A (p.Arg728=)	not specified [RCV004640956]	likely benign	14	75047472	75047472	Human		name
407486850	CV3457350	single nucleotide variant	NM_001040108.2(MLH3):c.2481A>T (p.Ser827=)	not specified [RCV004640957]	likely benign	14	75047175	75047175	Human		name
407486989	CV3457377	single nucleotide variant	NM_001040108.2(MLH3):c.285G>T (p.Glu95Asp)	not specified [RCV004640979]	uncertain significance	14	75049371	75049371	Human		name
407487009	CV3457380	single nucleotide variant	NM_001040108.2(MLH3):c.1917A>G (p.Gln639=)	not specified [RCV004640982]	likely benign	14	75047739	75047739	Human		name
407487033	CV3457384	single nucleotide variant	NM_001040108.2(MLH3):c.1683A>G (p.Gly561=)	not specified [RCV004640986]	likely benign	14	75047973	75047973	Human		name
408384610	CV3504406	duplication	NM_001040108.2(MLH3):c.437dup (p.Thr147fs)	MLH3-related disorder [RCV004731952]	uncertain significance	14	75049218	75049219	Human		name , trait , alternate_id
408377538	CV3508930	single nucleotide variant	NM_001040108.2(MLH3):c.2736C>T (p.Cys912=)	MLH3-related disorder [RCV004751064]\|not specified [RCV004824076]	likely benign	14	75046920	75046920	Human		name , alternate_id
597640909	CV3556971	single nucleotide variant	NM_001040108.2(MLH3):c.253G>A (p.Glu85Lys)	not specified [RCV004825366]	uncertain significance	14	75049403	75049403	Human		name
597636329	CV3556974	single nucleotide variant	NM_001040108.2(MLH3):c.2334C>T (p.Val778=)	not specified [RCV004824514]	likely benign	14	75047322	75047322	Human		name
597636335	CV3556977	single nucleotide variant	NM_001040108.2(MLH3):c.262A>G (p.Arg88Gly)	not specified [RCV004824515]	uncertain significance	14	75049394	75049394	Human		name
597640979	CV3556998	deletion	NM_001040108.2(MLH3):c.903del (p.Glu301fs)	not specified [RCV004825378]	uncertain significance	14	75048753	75048753	Human		name
597640992	CV3557002	single nucleotide variant	NM_001040108.2(MLH3):c.287C>G (p.Ala96Gly)	not specified [RCV004825381]	uncertain significance	14	75049369	75049369	Human		name
597641108	CV3557041	single nucleotide variant	NM_001040108.2(MLH3):c.2442A>G (p.Ser814=)	not specified [RCV004825401]	likely benign	14	75047214	75047214	Human		name
597636459	CV3557073	single nucleotide variant	NM_001040108.2(MLH3):c.257A>C (p.Asn86Thr)	not specified [RCV004824539]	uncertain significance	14	75049399	75049399	Human		name
597641244	CV3557077	single nucleotide variant	NM_001040108.2(MLH3):c.2013C>T (p.Asn671=)	not specified [RCV004825426]	likely benign	14	75047643	75047643	Human		name
597641274	CV3557088	single nucleotide variant	NM_001040108.2(MLH3):c.1626G>A (p.Leu542=)	not specified [RCV004825431]	likely benign	14	75048030	75048030	Human		name
597641284	CV3557090	single nucleotide variant	NM_001040108.2(MLH3):c.2829G>A (p.Gln943=)	not specified [RCV004825433]	likely benign	14	75046827	75046827	Human		name
597636496	CV3557094	single nucleotide variant	NM_001040108.2(MLH3):c.2406T>C (p.Asp802=)	not specified [RCV004824546]	likely benign	14	75047250	75047250	Human		name
597641306	CV3557095	single nucleotide variant	NM_001040108.2(MLH3):c.2841T>C (p.Phe947=)	not specified [RCV004825437]	likely benign	14	75046815	75046815	Human		name
597641312	CV3557096	single nucleotide variant	NM_001040108.2(MLH3):c.246G>C (p.Gln82His)	not specified [RCV004825438]	uncertain significance	14	75049410	75049410	Human		name
597641324	CV3557101	single nucleotide variant	NM_001040108.2(MLH3):c.1977C>T (p.Ala659=)	not specified [RCV004825440]	likely benign	14	75047679	75047679	Human		name
597641342	CV3557104	single nucleotide variant	NM_001040108.2(MLH3):c.1305A>T (p.Thr435=)	not specified [RCV004825443]	likely benign	14	75048351	75048351	Human		name
597641355	CV3557107	single nucleotide variant	NM_001040108.2(MLH3):c.214C>A (p.Arg72Ser)	not specified [RCV004825445]	uncertain significance	14	75049442	75049442	Human		name
597641370	CV3557111	single nucleotide variant	NM_001040108.2(MLH3):c.2145C>G (p.Pro715=)	not specified [RCV004825448]	likely benign	14	75047511	75047511	Human		name
597641383	CV3557113	single nucleotide variant	NM_001040108.2(MLH3):c.2706A>G (p.Ser902=)	not specified [RCV004825450]	likely benign	14	75046950	75046950	Human		name
597641393	CV3557115	single nucleotide variant	NM_001040108.2(MLH3):c.1599T>C (p.Thr533=)	not specified [RCV004825452]	likely benign	14	75048057	75048057	Human		name
597641451	CV3557130	single nucleotide variant	NM_001040108.2(MLH3):c.2910G>A (p.Leu970=)	not specified [RCV004825462]	likely benign	14	75046746	75046746	Human		name
597641524	CV3557149	single nucleotide variant	NM_001040108.2(MLH3):c.227G>C (p.Ser76Thr)	not specified [RCV004825474]	uncertain significance	14	75049429	75049429	Human		name
597641530	CV3557150	single nucleotide variant	NM_001040108.2(MLH3):c.241G>T (p.Val81Leu)	not specified [RCV004825475]	uncertain significance	14	75049415	75049415	Human		name
597641536	CV3557154	single nucleotide variant	NM_001040108.2(MLH3):c.2392T>C (p.Leu798=)	not specified [RCV004825476]	likely benign	14	75047264	75047264	Human		name
597641560	CV3557161	single nucleotide variant	NM_001040108.2(MLH3):c.2127A>C (p.Ile709=)	not specified [RCV004825480]	likely benign	14	75047529	75047529	Human		name
597676740	CV3710983	single nucleotide variant	NM_001040108.2(MLH3):c.155T>G (p.Val52Gly)	Endometrial carcinoma [RCV005005705]	uncertain significance	14	75049501	75049501	Human	2	name
597943993	CV3782728	single nucleotide variant	NM_001040108.2(MLH3):c.292G>A (p.Ala98Thr)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005134268]	uncertain significance	14	75049364	75049364	Human	1	name
597844524	CV3827473	single nucleotide variant	NM_001040108.2(MLH3):c.2961T>C (p.Leu987=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005172744]	likely benign	14	75046695	75046695	Human	1	name
597935856	CV3858915	single nucleotide variant	NM_001040108.2(MLH3):c.1008C>G (p.Leu336=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005207636]	likely benign	14	75048648	75048648	Human	1	name
598166578	CV3989358	single nucleotide variant	NM_001040108.2(MLH3):c.1857A>G (p.Lys619=)	not specified [RCV005369371]	likely benign	14	75047799	75047799	Human		name
598187848	CV3989392	single nucleotide variant	NM_001040108.2(MLH3):c.218A>G (p.Tyr73Cys)	not specified [RCV005373627]	uncertain significance	14	75049438	75049438	Human		name
598187880	CV3989406	single nucleotide variant	NM_001040108.2(MLH3):c.268T>C (p.Tyr90His)	not specified [RCV005373632]	uncertain significance	14	75049388	75049388	Human		name
598187900	CV3989410	single nucleotide variant	NM_001040108.2(MLH3):c.150C>A (p.Phe50Leu)	not specified [RCV005373635]	uncertain significance	14	75049506	75049506	Human		name
598187919	CV3989415	single nucleotide variant	NM_001040108.2(MLH3):c.2154C>T (p.Pro718=)	not specified [RCV005373638]	likely benign	14	75047502	75047502	Human		name
598187926	CV3989416	single nucleotide variant	NM_001040108.2(MLH3):c.1824T>C (p.Phe608=)	not specified [RCV005373639]	likely benign	14	75047832	75047832	Human		name
598166814	CV3989429	single nucleotide variant	NM_001040108.2(MLH3):c.164T>C (p.Ile55Thr)	not specified [RCV005369401]	uncertain significance	14	75049492	75049492	Human		name
598188030	CV3989438	single nucleotide variant	NM_001040108.2(MLH3):c.151C>T (p.Gln51Ter)	not specified [RCV005373655]	uncertain significance	14	75049505	75049505	Human		name
598188037	CV3989443	single nucleotide variant	NM_001040108.2(MLH3):c.2580T>C (p.Asn860=)	not specified [RCV005373656]	likely benign	14	75047076	75047076	Human		name
598166859	CV3989445	single nucleotide variant	NM_001040108.2(MLH3):c.2283T>C (p.Tyr761=)	not specified [RCV005369409]	likely benign	14	75047373	75047373	Human		name
598188061	CV3989449	single nucleotide variant	NM_001040108.2(MLH3):c.2541A>G (p.Arg847=)	not specified [RCV005373660]	likely benign	14	75047115	75047115	Human		name
598166870	CV3989450	single nucleotide variant	NM_001040108.2(MLH3):c.1275T>G (p.Ser425=)	not specified [RCV005369411]	likely benign	14	75048381	75048381	Human		name
598188087	CV3989456	single nucleotide variant	NM_001040108.2(MLH3):c.2136T>C (p.Asp712=)	not specified [RCV005373664]	likely benign	14	75047520	75047520	Human		name
598166908	CV3989466	single nucleotide variant	NM_001040108.2(MLH3):c.1899T>G (p.Pro633=)	not specified [RCV005369419]	likely benign	14	75047757	75047757	Human		name
12883558	CV399728	single nucleotide variant	NM_001040108.2(MLH3):c.1500G>A (p.Pro500=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000461834]\|MLH3-related disorder [RCV003970357]\|not specified [RCV004023056]	benign\|likely benign	14	75048156	75048156	Human	1	name , alternate_id
12889052	CV399738	single nucleotide variant	NM_001040108.2(MLH3):c.119G>A (p.Cys40Tyr)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000472084]\|not specified [RCV004022853]	uncertain significance	14	75049537	75049537	Human	1	name
12880905	CV400506	single nucleotide variant	NM_001040108.2(MLH3):c.2940C>T (p.Thr980=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001425569]\|not specified [RCV004023058]	likely benign	14	75046716	75046716	Human	1	name
598201196	CV4007574	single nucleotide variant	NM_001040108.2(MLH3):c.1533T>G (p.Pro511=)	Endometrial carcinoma [RCV005398406]	likely benign	14	75048123	75048123	Human	2	name
13477629	CV463497	single nucleotide variant	NM_001040108.2(MLH3):c.277C>G (p.Arg93Gly)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001119975]\|not specified [RCV004024418]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75049379	75049379	Human	1	name
13475756	CV464088	single nucleotide variant	NM_001040108.2(MLH3):c.2574C>A (p.Leu858=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000548865]	likely benign	14	75047082	75047082	Human	1	name
13494946	CV464497	single nucleotide variant	NM_001040108.2(MLH3):c.184G>A (p.Gly62Arg)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000559273]\|MLH3-related disorder [RCV003935562]\|not specified [RCV004024415]	likely benign	14	75049472	75049472	Human	1	name , alternate_id
13626834	CV528370	single nucleotide variant	NM_001040108.2(MLH3):c.2241G>A (p.Leu747=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000655411]\|MLH3-related disorder [RCV003918096]\|not specified [RCV004025975]	likely benign	14	75047415	75047415	Human	1	name , alternate_id
13626828	CV528734	single nucleotide variant	NM_001040108.2(MLH3):c.2760T>C (p.Cys920=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000655405]\|not specified [RCV004025971]	likely benign	14	75046896	75046896	Human	1	name
13626827	CV528827	single nucleotide variant	NM_001040108.2(MLH3):c.2547T>C (p.Ser849=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000655404]\|Endometrial carcinoma [RCV005392251]\|MLH3-related disorder [RCV003907921]\|not specified [RCV002268241]	likely benign	14	75047109	75047109	Human	5	name , alternate_id
13803059	CV568279	duplication	NM_001040108.2(MLH3):c.487dup (p.Asp163fs)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000698852]	uncertain significance	14	75049168	75049169	Human	1	name
14733740	CV642727	single nucleotide variant	NM_001040108.2(MLH3):c.277C>T (p.Arg93Ter)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000802408]\|not specified [RCV004028109]	uncertain significance	14	75049379	75049379	Human	1	name
14719832	CV642728	single nucleotide variant	NM_001040108.2(MLH3):c.236A>G (p.His79Arg)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000796376]\|not specified [RCV004027563]	uncertain significance	14	75049420	75049420	Human	1	name
15130834	CV684525	single nucleotide variant	NM_001040108.2(MLH3):c.1002C>T (p.Asp334=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000863502]\|Endometrial carcinoma [RCV005392472]\|not specified [RCV004029338]	likely benign	14	75048654	75048654	Human	4	name
15101740	CV688360	single nucleotide variant	NM_001040108.2(MLH3):c.2874T>C (p.Asn958=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001441653]\|not specified [RCV004027773]	likely benign	14	75046782	75046782	Human	1	name
15155514	CV688361	single nucleotide variant	NM_001040108.2(MLH3):c.2493A>G (p.Pro831=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000868056]\|not specified [RCV004027711]	likely benign	14	75047163	75047163	Human	1	name
15140217	CV688363	single nucleotide variant	NM_001040108.2(MLH3):c.2166C>T (p.His722=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000865139]\|MLH3-related disorder [RCV003892808]\|not specified [RCV004027644]	likely benign	14	75047490	75047490	Human	1	name , alternate_id
15137022	CV688364	single nucleotide variant	NM_001040108.2(MLH3):c.2043T>C (p.Tyr681=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000864596]\|Endometrial carcinoma [RCV005392474]\|MLH3-related disorder [RCV003965684]\|not specified [RCV002268340]	benign\|likely benign	14	75047613	75047613	Human	5	name , alternate_id
15160047	CV688365	single nucleotide variant	NM_001040108.2(MLH3):c.1899T>C (p.Pro633=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001477228]\|not specified [RCV004027744]	likely benign	14	75047757	75047757	Human	1	name
15154333	CV688366	single nucleotide variant	NM_001040108.2(MLH3):c.1794T>C (p.Tyr598=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000867831]\|not specified [RCV004027706]	likely benign	14	75047862	75047862	Human	1	name
15097780	CV688367	single nucleotide variant	NM_001040108.2(MLH3):c.1152C>T (p.Ser384=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001470520]\|Endometrial carcinoma [RCV005392482]\|MLH3-related disorder [RCV004751765]\|not specified [RCV004027754]	likely benign\|uncertain significance	14	75048504	75048504	Human	5	name , alternate_id
15150870	CV688368	single nucleotide variant	NM_001040108.2(MLH3):c.1017C>T (p.Cys339=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001467491]\|Endometrial carcinoma [RCV005392477]\|MLH3-related disorder [RCV003892823]\|not provided [RCV003392646]\|not specified [RCV004027691]	likely benign	14	75048639	75048639	Human	5	name , alternate_id
15188430	CV702991	single nucleotide variant	NM_001040108.2(MLH3):c.1740G>A (p.Glu580=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000953877]\|not specified [RCV004029852]	likely benign	14	75047916	75047916	Human	1	name
15176104	CV725812	single nucleotide variant	NM_001040108.2(MLH3):c.1683A>T (p.Gly561=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001465342]\|not specified [RCV004028338]	likely benign	14	75047973	75047973	Human	1	name
15200891	CV725813	single nucleotide variant	NM_001040108.2(MLH3):c.1671T>C (p.Ala557=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000891038]\|not specified [RCV004028400]	likely benign	14	75047985	75047985	Human	1	name
15098276	CV725814	single nucleotide variant	NM_001040108.2(MLH3):c.1482T>C (p.His494=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000891696]\|not specified [RCV004028410]	likely benign	14	75048174	75048174	Human	1	name
15124038	CV739335	single nucleotide variant	NM_001040108.2(MLH3):c.1470T>C (p.Ser490=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001426084]\|not specified [RCV004028464]	likely benign	14	75048186	75048186	Human	1	name
15184468	CV739336	single nucleotide variant	NM_001040108.2(MLH3):c.1257C>T (p.Asn419=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002068664]\|not specified [RCV004028588]	likely benign	14	75048399	75048399	Human	1	name
15126984	CV739337	single nucleotide variant	NM_001040108.2(MLH3):c.1110T>G (p.Gly370=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001503187]\|not specified [RCV004028468]	likely benign	14	75048546	75048546	Human	1	name
15164141	CV754163	single nucleotide variant	NM_001040108.2(MLH3):c.2193T>C (p.Asp731=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001445341]\|not specified [RCV004029516]	likely benign	14	75047463	75047463	Human	1	name
26895399	CV841774	single nucleotide variant	NM_001040108.2(MLH3):c.285G>C (p.Glu95Asp)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001064005]\|not specified [RCV004030518]	uncertain significance	14	75049371	75049371	Human	1	name
28893878	CV872668	single nucleotide variant	NM_001040108.2(MLH3):c.2128T>C (p.Leu710=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001121870]\|not specified [RCV004032231]	likely benign\|uncertain significance	14	75047528	75047528	Human	1	name
28883490	CV872672	single nucleotide variant	NM_001040108.2(MLH3):c.1125T>C (p.Asp375=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001118459]\|not specified [RCV004032209]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75048531	75048531	Human	1	name
38490772	CV927173	single nucleotide variant	NM_001040108.2(MLH3):c.278G>A (p.Arg93Gln)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001222381]\|Endometrial carcinoma [RCV003142178]\|not specified [RCV004032442]	uncertain significance	14	75049378	75049378	Human	3	name
38493940	CV927174	single nucleotide variant	NM_001040108.2(MLH3):c.127G>A (p.Val43Ile)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001224621]	uncertain significance	14	75049529	75049529	Human	1	name
126745551	CV995978	deletion	NM_001040108.2(MLH3):c.615del (p.Asp206fs)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001296471]\|not specified [RCV004036034]	uncertain significance	14	75049041	75049041	Human	1	name
126729270	CV995980	single nucleotide variant	NM_001040108.2(MLH3):c.244C>T (p.Gln82Ter)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001303540]\|Endometrial carcinoma [RCV005005146]	uncertain significance	14	75049412	75049412	Human	4	name
405232064	CV3144620	single nucleotide variant	NM_001040108.2(MLH3):c.3306T>C (p.Phe1102=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003853073]\|not specified [RCV004828002]	likely benign	14	75042452	75042452	Human	1	name
405247726	CV3159092	single nucleotide variant	NM_001040108.2(MLH3):c.651G>C (p.Leu217Phe)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003869237]	uncertain significance	14	75049005	75049005	Human	1	name
405292819	CV3217526	single nucleotide variant	NM_001040108.2(MLH3):c.4051C>T (p.Leu1351=)	MLH3-related disorder [RCV003964759]	likely benign	14	75022853	75022853	Human		name , trait , alternate_id
405711209	CV3359532	single nucleotide variant	NM_001040108.2(MLH3):c.895A>G (p.Thr299Ala)	not specified [RCV004493880]	uncertain significance	14	75048761	75048761	Human		name
405726871	CV3359560	single nucleotide variant	NM_001040108.2(MLH3):c.928G>A (p.Val310Met)	not specified [RCV004495892]	uncertain significance	14	75048728	75048728	Human		name
405702962	CV3388931	single nucleotide variant	NM_001040108.2(MLH3):c.748C>A (p.Gln250Lys)	not specified [RCV004521268]	uncertain significance	14	75048908	75048908	Human		name
405702970	CV3388932	single nucleotide variant	NM_001040108.2(MLH3):c.788A>T (p.Lys263Met)	not specified [RCV004521269]	uncertain significance	14	75048868	75048868	Human		name
405702976	CV3388933	single nucleotide variant	NM_001040108.2(MLH3):c.789G>T (p.Lys263Asn)	not specified [RCV004521270]	uncertain significance	14	75048867	75048867	Human		name
405702989	CV3388935	single nucleotide variant	NM_001040108.2(MLH3):c.828T>A (p.Ser276Arg)	not specified [RCV004521272]	uncertain significance	14	75048828	75048828	Human		name
405703006	CV3388937	single nucleotide variant	NM_001040108.2(MLH3):c.870G>A (p.Met290Ile)	not specified [RCV004521274]	uncertain significance	14	75048786	75048786	Human		name
405702300	CV3392299	duplication	NM_001040108.2(MLH3):c.2788dup (p.Thr930fs)	not specified [RCV004521174]	uncertain significance	14	75046867	75046868	Human		name
405702439	CV3392320	single nucleotide variant	NM_001040108.2(MLH3):c.308T>C (p.Met103Thr)	not specified [RCV004521194]	uncertain significance	14	75049348	75049348	Human		name
405702451	CV3392322	single nucleotide variant	NM_001040108.2(MLH3):c.3096T>C (p.Ser1032=)	not specified [RCV004521196]	likely benign	14	75046560	75046560	Human		name
405702461	CV3392324	single nucleotide variant	NM_001040108.2(MLH3):c.3102T>A (p.Thr1034=)	not specified [RCV004521198]	likely benign	14	75046554	75046554	Human		name
405702508	CV3392330	single nucleotide variant	NM_001040108.2(MLH3):c.316G>C (p.Ala106Pro)	not specified [RCV004521204]	uncertain significance	14	75049340	75049340	Human		name
405702545	CV3392335	single nucleotide variant	NM_001040108.2(MLH3):c.3315C>T (p.Asp1105=)	not specified [RCV004521209]	likely benign	14	75042443	75042443	Human		name
405702553	CV3392336	single nucleotide variant	NM_001040108.2(MLH3):c.3351G>A (p.Glu1117=)	not specified [RCV004521210]	likely benign	14	75042407	75042407	Human		name
407486675	CV3457315	single nucleotide variant	NM_001040108.2(MLH3):c.934T>G (p.Cys312Gly)	not specified [RCV004640930]	uncertain significance	14	75048722	75048722	Human		name
407518669	CV3457316	single nucleotide variant	NM_001040108.2(MLH3):c.718A>G (p.Ser240Gly)	not specified [RCV004628951]	uncertain significance	14	75048938	75048938	Human		name
407486745	CV3457328	single nucleotide variant	NM_001040108.2(MLH3):c.506A>G (p.Glu169Gly)	not specified [RCV004640940]	uncertain significance	14	75049150	75049150	Human		name
407518698	CV3457354	single nucleotide variant	NM_001040108.2(MLH3):c.839A>G (p.Lys280Arg)	not specified [RCV004628960]	uncertain significance	14	75048817	75048817	Human		name
407486878	CV3457357	single nucleotide variant	NM_001040108.2(MLH3):c.644A>C (p.Tyr215Ser)	not specified [RCV004640962]	uncertain significance	14	75049012	75049012	Human		name
407518707	CV3457367	single nucleotide variant	NM_001040108.2(MLH3):c.3159A>G (p.Gly1053=)	not specified [RCV004628963]	likely benign	14	75046497	75046497	Human		name
407486995	CV3457378	single nucleotide variant	NM_001040108.2(MLH3):c.877A>C (p.Ser293Arg)	not specified [RCV004640980]	uncertain significance	14	75048779	75048779	Human		name
407487083	CV3457393	single nucleotide variant	NM_001040108.2(MLH3):c.488A>G (p.Asp163Gly)	not specified [RCV004640994]	uncertain significance	14	75049168	75049168	Human		name
407487125	CV3457399	single nucleotide variant	NM_001040108.2(MLH3):c.3652C>T (p.Leu1218=)	not specified [RCV004641000]	likely benign	14	75033482	75033482	Human		name
407518714	CV3457401	single nucleotide variant	NM_001040108.2(MLH3):c.677T>C (p.Ile226Thr)	not specified [RCV004628965]	uncertain significance	14	75048979	75048979	Human		name
407518720	CV3457403	single nucleotide variant	NM_001040108.2(MLH3):c.3282G>A (p.Gly1094=)	not specified [RCV004628967]	likely benign	14	75042476	75042476	Human		name
407487138	CV3457404	single nucleotide variant	NM_001040108.2(MLH3):c.4260T>A (p.Thr1420=)	not specified [RCV004641002]	likely benign	14	75017184	75017184	Human		name
407487181	CV3457414	single nucleotide variant	NM_001040108.2(MLH3):c.652G>A (p.Gly218Arg)	not specified [RCV004641010]	uncertain significance	14	75049004	75049004	Human		name
407487191	CV3457416	single nucleotide variant	NM_001040108.2(MLH3):c.958T>C (p.Cys320Arg)	not specified [RCV004641012]	uncertain significance	14	75048698	75048698	Human		name
597640897	CV3556967	single nucleotide variant	NM_001040108.2(MLH3):c.4302A>G (p.Lys1434=)	not specified [RCV004825364]	likely benign	14	75017142	75017142	Human		name
597636351	CV3556984	single nucleotide variant	NM_001040108.2(MLH3):c.804T>G (p.Ile268Met)	not specified [RCV004824518]	uncertain significance	14	75048852	75048852	Human		name
597640930	CV3556987	single nucleotide variant	NM_001040108.2(MLH3):c.908A>G (p.Tyr303Cys)	not specified [RCV004825370]	uncertain significance	14	75048748	75048748	Human		name
597640938	CV3556988	single nucleotide variant	NM_001040108.2(MLH3):c.956T>C (p.Val319Ala)	not specified [RCV004825371]	uncertain significance	14	75048700	75048700	Human		name
597626822	CV3557005	single nucleotide variant	NM_001040108.2(MLH3):c.905T>G (p.Leu302Arg)	Endometrial carcinoma [RCV005003814]\|not specified [RCV004825383]	uncertain significance	14	75048751	75048751	Human	2	name
597641004	CV3557006	single nucleotide variant	NM_001040108.2(MLH3):c.803T>C (p.Ile268Thr)	not specified [RCV004825384]	uncertain significance	14	75048853	75048853	Human		name
597641029	CV3557017	single nucleotide variant	NM_001040108.2(MLH3):c.3825A>G (p.Leu1275=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005358163]\|not specified [RCV004825388]	likely benign	14	75032070	75032070	Human	2	name
597641041	CV3557022	single nucleotide variant	NM_001040108.2(MLH3):c.4044A>G (p.Thr1348=)	not specified [RCV004825390]	likely benign	14	75022860	75022860	Human		name
597641054	CV3557024	single nucleotide variant	NM_001040108.2(MLH3):c.3411G>T (p.Ser1137=)	not specified [RCV004825392]	likely benign	14	75041669	75041669	Human		name
597636398	CV3557027	single nucleotide variant	NM_001040108.2(MLH3):c.647G>A (p.Gly216Glu)	not specified [RCV004824527]	uncertain significance	14	75049009	75049009	Human		name
597641130	CV3557045	single nucleotide variant	NM_001040108.2(MLH3):c.586T>C (p.Ser196Pro)	not specified [RCV004825405]	uncertain significance	14	75049070	75049070	Human		name
597641208	CV3557065	deletion	NM_001040108.2(MLH3):c.1287del (p.Ala430fs)	not specified [RCV004825420]	uncertain significance	14	75048369	75048369	Human		name
597636447	CV3557069	single nucleotide variant	NM_001040108.2(MLH3):c.595C>T (p.Leu199Phe)	not specified [RCV004824537]	uncertain significance	14	75049061	75049061	Human		name
597641221	CV3557071	single nucleotide variant	NM_001040108.2(MLH3):c.766A>G (p.Lys256Glu)	not specified [RCV004825422]	uncertain significance	14	75048890	75048890	Human		name
597641226	CV3557072	single nucleotide variant	NM_001040108.2(MLH3):c.3339A>G (p.Arg1113=)	not specified [RCV004825423]	likely benign	14	75042419	75042419	Human		name
597636482	CV3557083	single nucleotide variant	NM_001040108.2(MLH3):c.494G>A (p.Arg165Lys)	not specified [RCV004824543]	uncertain significance	14	75049162	75049162	Human		name
597636486	CV3557085	single nucleotide variant	NM_001040108.2(MLH3):c.3984G>A (p.Val1328=)	not specified [RCV004824544]	likely benign	14	75030546	75030546	Human		name
597641290	CV3557091	single nucleotide variant	NM_001040108.2(MLH3):c.4215C>T (p.Asp1405=)	not specified [RCV004825434]	likely benign	14	75018856	75018856	Human		name
597641404	CV3557119	single nucleotide variant	NM_001040108.2(MLH3):c.4059C>G (p.Val1353=)	not specified [RCV004825454]	likely benign	14	75022845	75022845	Human		name
597641416	CV3557121	single nucleotide variant	NM_001040108.2(MLH3):c.515G>A (p.Arg172Lys)	not specified [RCV004825456]	uncertain significance	14	75049141	75049141	Human		name
597641433	CV3557126	single nucleotide variant	NM_001040108.2(MLH3):c.460C>T (p.Gln154Ter)	not specified [RCV004825459]	uncertain significance	14	75049196	75049196	Human		name
597641447	CV3557129	single nucleotide variant	NM_001040108.2(MLH3):c.971C>A (p.Ala324Asp)	not specified [RCV004825461]	uncertain significance	14	75048685	75048685	Human		name
597641473	CV3557134	single nucleotide variant	NM_001040108.2(MLH3):c.703C>G (p.Leu235Val)	not specified [RCV004825466]	uncertain significance	14	75048953	75048953	Human		name
597641488	CV3557137	single nucleotide variant	NM_001040108.2(MLH3):c.917A>C (p.Tyr306Ser)	not specified [RCV004825468]	uncertain significance	14	75048739	75048739	Human		name
597641500	CV3557141	single nucleotide variant	NM_001040108.2(MLH3):c.3999A>G (p.Arg1333=)	not specified [RCV004825470]	likely benign	14	75023007	75023007	Human		name
597636573	CV3557152	single nucleotide variant	NM_001040108.2(MLH3):c.4182T>C (p.Ala1394=)	not specified [RCV004824560]	likely benign	14	75018889	75018889	Human		name
597690047	CV3710982	single nucleotide variant	NM_001040108.2(MLH3):c.932A>G (p.Gln311Arg)	Endometrial carcinoma [RCV005007305]	uncertain significance	14	75048724	75048724	Human	2	name
597841530	CV3752849	single nucleotide variant	NM_001040108.2(MLH3):c.600G>C (p.Gln200His)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005086578]	uncertain significance	14	75049056	75049056	Human	1	name
597892302	CV3758938	single nucleotide variant	NM_001040108.2(MLH3):c.936C>G (p.Cys312Trp)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005071294]	uncertain significance	14	75048720	75048720	Human	1	name
597933619	CV3793427	duplication	NM_001040108.2(MLH3):c.1532dup (p.Gln513fs)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005132083]	uncertain significance	14	75048123	75048124	Human	1	name
597946191	CV3841596	single nucleotide variant	NM_001040108.2(MLH3):c.413C>G (p.Thr138Ser)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005189029]	uncertain significance	14	75049243	75049243	Human	1	name
597948274	CV3852464	single nucleotide variant	NM_001040108.2(MLH3):c.644A>G (p.Tyr215Cys)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV005189542]	uncertain significance	14	75049012	75049012	Human	1	name
598124327	CV3881461	duplication	NM_001040108.2(MLH3):c.1729dup (p.Ala577fs)	not provided [RCV005231886]	likely pathogenic	14	75047926	75047927	Human		name
598226733	CV3895843	deletion	NM_001040108.2(MLH3):c.1619del (p.Asn540fs)	Colorectal cancer [RCV005362134]	pathogenic	14	75048037	75048037	Human	2	name
598166593	CV3989360	single nucleotide variant	NM_001040108.2(MLH3):c.683T>C (p.Phe228Ser)	not specified [RCV005369373]	uncertain significance	14	75048973	75048973	Human		name
598187765	CV3989370	single nucleotide variant	NM_001040108.2(MLH3):c.406G>A (p.Asp136Asn)	not specified [RCV005373614]	uncertain significance	14	75049250	75049250	Human		name
598187811	CV3989384	single nucleotide variant	NM_001040108.2(MLH3):c.641T>G (p.Ile214Ser)	not specified [RCV005373621]	uncertain significance	14	75049015	75049015	Human		name
598187836	CV3989389	single nucleotide variant	NM_001040108.2(MLH3):c.992A>T (p.Gln331Leu)	not specified [RCV005373625]	uncertain significance	14	75048664	75048664	Human		name
598166691	CV3989390	single nucleotide variant	NM_001040108.2(MLH3):c.4278C>G (p.Ala1426=)	not specified [RCV005369386]	likely benign	14	75017166	75017166	Human		name
598166699	CV3989393	single nucleotide variant	NM_001040108.2(MLH3):c.3114C>T (p.Asn1038=)	not specified [RCV005369387]	likely benign	14	75046542	75046542	Human		name
598166740	CV3989401	single nucleotide variant	NM_001040108.2(MLH3):c.4170A>T (p.Pro1390=)	not specified [RCV005369392]	likely benign	14	75018901	75018901	Human		name
598187887	CV3989407	single nucleotide variant	NM_001040108.2(MLH3):c.3823T>C (p.Leu1275=)	not specified [RCV005373633]	likely benign	14	75032072	75032072	Human		name
598166785	CV3989411	single nucleotide variant	NM_001040108.2(MLH3):c.437T>C (p.Val146Ala)	not specified [RCV005369397]	uncertain significance	14	75049219	75049219	Human		name
598187907	CV3989412	single nucleotide variant	NM_001040108.2(MLH3):c.3390T>C (p.Asp1130=)	not specified [RCV005373636]	likely benign	14	75041690	75041690	Human		name
598187913	CV3989413	single nucleotide variant	NM_001040108.2(MLH3):c.3027A>C (p.Val1009=)	not specified [RCV005373637]	likely benign	14	75046629	75046629	Human		name
598187951	CV3989422	single nucleotide variant	NM_001040108.2(MLH3):c.3996C>T (p.Ile1332=)	not specified [RCV005373643]	likely benign	14	75023010	75023010	Human		name
598187977	CV3989426	single nucleotide variant	NM_001040108.2(MLH3):c.767A>G (p.Lys256Arg)	not specified [RCV005373647]	uncertain significance	14	75048889	75048889	Human		name
598166819	CV3989432	single nucleotide variant	NM_001040108.2(MLH3):c.544C>G (p.His182Asp)	not specified [RCV005369402]	uncertain significance	14	75049112	75049112	Human		name
598188017	CV3989436	single nucleotide variant	NM_001040108.2(MLH3):c.3669T>C (p.Asp1223=)	not specified [RCV005373653]	likely benign	14	75033465	75033465	Human		name
598166853	CV3989442	single nucleotide variant	NM_001040108.2(MLH3):c.524T>C (p.Ile175Thr)	not specified [RCV005369408]	uncertain significance	14	75049132	75049132	Human		name
598188055	CV3989448	single nucleotide variant	NM_001040108.2(MLH3):c.3916C>T (p.Leu1306=)	not specified [RCV005373659]	likely benign	14	75030614	75030614	Human		name
598201254	CV4007583	single nucleotide variant	NM_001040108.2(MLH3):c.446A>G (p.Tyr149Cys)	Endometrial carcinoma [RCV005398415]	uncertain significance	14	75049210	75049210	Human	2	name
126735626	CV1031706	single nucleotide variant	NM_001040108.2(MLH3):c.3974A>G (p.Lys1325Arg)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001350112]\|MLH3-related disorder [RCV003963236]\|not specified [RCV004036608]	uncertain significance	14	75030556	75030556	Human	1	alternate_id
126924166	CV1048669	single nucleotide variant	NM_001040108.2(MLH3):c.1306A>G (p.Asn436Asp)	Colorectal cancer [RCV005361570]\|Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001366710]\|Endometrial carcinoma [RCV005005211]\|MLH3-related disorder [RCV003908551]\|not specified [RCV004036982]	conflicting interpretations of pathogenicity\|uncertain significance	14	75048350	75048350	Human	5	alternate_id
127329512	CV1144832	single nucleotide variant	NM_001040108.2(MLH3):c.3117G>A (p.Thr1039=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001487451]\|MLH3-related disorder [RCV003908745]\|not specified [RCV004037280]	likely benign	14	75046539	75046539	Human	1	alternate_id
127305830	CV1144836	single nucleotide variant	NM_001040108.2(MLH3):c.2180G>A (p.Ser727Asn)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001500010]\|Endometrial carcinoma [RCV005395040]\|MLH3-related disorder [RCV003900724]\|not specified [RCV004037405]	likely benign\|uncertain significance	14	75047476	75047476	Human	5	alternate_id
127289853	CV1152611	single nucleotide variant	NM_001040108.2(MLH3):c.1384G>A (p.Asp462Asn)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001865966]\|MLH3-related disorder [RCV003416375]\|not provided [RCV001509473]\|not specified [RCV004037912]	uncertain significance	14	75048272	75048272	Human	1	alternate_id
151797997	CV1377269	single nucleotide variant	NM_001040108.2(MLH3):c.3840A>C (p.Lys1280Asn)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001917447]\|MLH3-related disorder [RCV004752090]\|not specified [RCV004039124]	uncertain significance	14	75030690	75030690	Human	1	alternate_id
151771309	CV1431277	single nucleotide variant	NM_001040108.2(MLH3):c.1223C>A (p.Ser408Ter)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001915000]\|Endometrial carcinoma [RCV005397124]\|MLH3-related disorder [RCV003401851]	uncertain significance	14	75048433	75048433	Human	5	alternate_id
151776545	CV1440337	single nucleotide variant	NM_001040108.2(MLH3):c.3676G>A (p.Ala1226Thr)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001874961]\|Endometrial carcinoma [RCV002478196]\|MLH3-related disorder [RCV003401811]\|not specified [RCV004040571]	uncertain significance	14	75033458	75033458	Human	5	alternate_id
151887124	CV1441463	single nucleotide variant	NM_001040108.2(MLH3):c.4155C>T (p.Ser1385=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001962907]\|MLH3-related disorder [RCV003968661]\|not specified [RCV004044369]	likely benign	14	75018916	75018916	Human	1	alternate_id
151788039	CV1495669	single nucleotide variant	NM_001040108.2(MLH3):c.1142G>A (p.Arg381His)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002026936]\|Endometrial carcinoma [RCV005008431]\|MLH3-related disorder [RCV003418343]\|not specified [RCV004046873]	likely benign\|uncertain significance	14	75048514	75048514	Human	5	alternate_id
151796941	CV1505689	single nucleotide variant	NM_001040108.2(MLH3):c.2218A>G (p.Ile740Val)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002047632]\|MLH3-related disorder [RCV003416497]\|not specified [RCV004038937]	uncertain significance	14	75047438	75047438	Human	1	alternate_id
152077010	CV1536309	single nucleotide variant	NM_001040108.2(MLH3):c.3786G>A (p.Pro1262=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002148818]\|MLH3-related disorder [RCV003903562]\|not specified [RCV004047009]	likely benign	14	75032109	75032109	Human	1	alternate_id
152086249	CV1589731	single nucleotide variant	NM_001040108.2(MLH3):c.4026C>T (p.Thr1342=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV002193675]\|MLH3-related disorder [RCV003971156]\|not specified [RCV004047110]	likely benign	14	75022878	75022878	Human	1	alternate_id
9686672	CV171170	single nucleotide variant	NM_001040108.2(MLH3):c.2449A>G (p.Ser817Gly)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000467821]\|Colorectal cancer, non-polyposis [RCV000148625]\|MLH3-related disorder [RCV003927450]\|not provided [RCV001354134]\|not specified [RCV002267888]	likely benign\|uncertain significance	14	75047207	75047207	Human	2	alternate_id
155679001	CV1786814	single nucleotide variant	NM_001040108.2(MLH3):c.3731A>C (p.Gln1244Pro)	MLH3-related disorder [RCV003408234]\|not specified [RCV004049785]	uncertain significance	14	75032164	75032164	Human		alternate_id
155701013	CV1788231	single nucleotide variant	NM_001040108.2(MLH3):c.3186T>C (p.Thr1062=)	MLH3-related disorder [RCV003960995]\|not specified [RCV004048871]	likely benign	14	75046470	75046470	Human		alternate_id
155701642	CV1788326	single nucleotide variant	NM_001040108.2(MLH3):c.3193A>G (p.Ser1065Gly)	MLH3-related disorder [RCV003943355]\|not specified [RCV004048896]	uncertain significance	14	75046463	75046463	Human		alternate_id
155710285	CV1795020	single nucleotide variant	NM_001040108.2(MLH3):c.3246G>C (p.Leu1082=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003099328]\|MLH3-related disorder [RCV003896122]\|not specified [RCV004049335]	likely benign	14	75046410	75046410	Human	1	alternate_id
155674269	CV1828770	single nucleotide variant	NM_001040108.2(MLH3):c.983T>C (p.Ile328Thr)	MLH3-related disorder [RCV004750735]\|not specified [RCV004057640]	uncertain significance	14	75048673	75048673	Human		alternate_id
155731256	CV1838496	single nucleotide variant	NM_001040108.2(MLH3):c.1774A>G (p.Arg592Gly)	MLH3-related disorder [RCV004750738]\|not specified [RCV004061409]	likely benign\|uncertain significance	14	75047882	75047882	Human		alternate_id
155678389	CV1841903	single nucleotide variant	NM_001040108.2(MLH3):c.2506G>A (p.Glu836Lys)	MLH3-related disorder [RCV004750745]\|not specified [RCV004062040]	uncertain significance	14	75047150	75047150	Human		alternate_id
155676068	CV1843354	single nucleotide variant	NM_001040108.2(MLH3):c.1071A>C (p.Leu357Phe)	MLH3-related disorder [RCV004750741]\|not specified [RCV004061535]	uncertain significance	14	75048585	75048585	Human		alternate_id
11348990	CV241878	single nucleotide variant	NM_001040108.2(MLH3):c.2924A>G (p.Asn975Ser)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000268025]\|Endometrial carcinoma [RCV005396756]\|MLH3-related disorder [RCV003907856]\|not provided [RCV004705055]\|not specified [RCV004020771]	benign\|likely benign\|uncertain significance	14	75046732	75046732	Human	5	alternate_id
11348164	CV241881	single nucleotide variant	NM_001040108.2(MLH3):c.1637G>T (p.Arg546Ile)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000234607]\|Endometrial carcinoma [RCV005235152]\|Endometrial carcinoma [RCV005396754]\|MLH3-related disorder [RCV003919927]\|not provided [RCV003237789]\|not specified [RCV002465581]	pathogenic\|benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75048019	75048019	Human	5	alternate_id
11349447	CV241882	single nucleotide variant	NM_001040108.2(MLH3):c.1258G>A (p.Val420Ile)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000405727]\|Endometrial carcinoma [RCV005235151]\|MLH3-related disorder [RCV003919926]\|not provided [RCV001354254]\|not specified [RCV001795360]	benign\|likely benign	14	75048398	75048398	Human	3	alternate_id
11346739	CV241884	single nucleotide variant	NM_001040108.2(MLH3):c.713A>C (p.Tyr238Ser)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000318893]\|MLH3-related disorder [RCV004751388]\|not provided [RCV001354755]\|not specified [RCV003321560]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75048943	75048943	Human	1	alternate_id
329390061	CV2465739	duplication	NM_001040108.2(MLH3):c.3113dup (p.Asn1038fs)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003779768]\|MLH3-related disorder [RCV003396953]\|not specified [RCV004283395]	uncertain significance	14	75046542	75046543	Human	1	alternate_id
401775247	CV2724033	duplication	NM_001040108.2(MLH3):c.1788_1803dup (p.Lys602Ter)	MLH3-related disorder [RCV003420648]\|not specified [RCV004326177]	uncertain significance	14	75047852	75047853	Human		alternate_id
401937631	CV2798891	single nucleotide variant	NM_001040108.2(MLH3):c.565T>G (p.Leu189Val)	MLH3-related disorder [RCV003416721]	uncertain significance	14	75049091	75049091	Human		trait , alternate_id
401912522	CV2800600	single nucleotide variant	NM_001040108.2(MLH3):c.4192C>T (p.Pro1398Ser)	MLH3-related disorder [RCV003399873]	uncertain significance	14	75018879	75018879	Human		trait , alternate_id
401908222	CV2801309	single nucleotide variant	NM_001040108.2(MLH3):c.3692T>G (p.Ile1231Arg)	MLH3-related disorder [RCV003397550]\|not specified [RCV004362821]	uncertain significance	14	75033442	75033442	Human		alternate_id
405285415	CV3212408	single nucleotide variant	NM_001040108.2(MLH3):c.2410T>A (p.Cys804Ser)	MLH3-related disorder [RCV003959014]\|not specified [RCV004828011]	uncertain significance	14	75047246	75047246	Human		alternate_id
11634525	CV321390	single nucleotide variant	NM_001040108.2(MLH3):c.3384T>C (p.Thr1128=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000364858]\|MLH3-related disorder [RCV004751456]\|not specified [RCV004639210]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75041696	75041696	Human	1	alternate_id
11634555	CV321394	single nucleotide variant	NM_001040108.2(MLH3):c.2159A>G (p.Tyr720Cys)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000404396]\|Endometrial carcinoma [RCV005235257]\|Endometrial carcinoma [RCV005396949]\|MLH3-related disorder [RCV003972341]\|not provided [RCV001636891]\|not specified [RCV000582541]	benign\|likely benign	14	75047497	75047497	Human	5	alternate_id
11634493	CV337243	single nucleotide variant	NM_001040108.2(MLH3):c.3440A>T (p.Asn1147Ile)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001094469]\|Endometrial carcinoma [RCV005396946]\|Hereditary cancer [RCV004701405]\|Lynch syndrome [RCV000269033]\|MLH3-related disorder [RCV004751455]\|not provided [RCV002261047]\|not specified [RCV003321583]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75041640	75041640	Human	7	alternate_id
11634462	CV339201	single nucleotide variant	NM_001040108.2(MLH3):c.2825C>T (p.Thr942Ile)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000280903]\|Endometrial carcinoma [RCV005235255]\|Endometrial carcinoma [RCV005396947]\|MLH3-related disorder [RCV003972340]\|not provided [RCV001660644]\|not specified [RCV000583593]	benign\|likely benign	14	75046831	75046831	Human	5	alternate_id
408383312	CV3503788	single nucleotide variant	NM_001040108.2(MLH3):c.2386A>G (p.Asn796Asp)	MLH3-related disorder [RCV004730561]	uncertain significance	14	75047270	75047270	Human		trait , alternate_id
408377496	CV3508229	single nucleotide variant	NM_001040108.2(MLH3):c.2542G>C (p.Glu848Gln)	MLH3-related disorder [RCV004751030]	uncertain significance	14	75047114	75047114	Human		trait , alternate_id
12850357	CV362739	single nucleotide variant	NM_001040108.2(MLH3):c.713A>G (p.Tyr238Cys)	Colorectal cancer [RCV000417245]\|Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001865317]\|MLH3-related disorder [RCV003418105]\|not specified [RCV004022194]	uncertain significance	14	75048943	75048943	Human	3	alternate_id
12888939	CV399719	single nucleotide variant	NM_001040108.2(MLH3):c.4301A>G (p.Lys1434Arg)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000471865]\|Endometrial carcinoma [RCV005010364]\|MLH3-related disorder [RCV003899929]\|not provided [RCV005230405]\|not specified [RCV004022840]	uncertain significance	14	75017143	75017143	Human	5	alternate_id
12889291	CV399908	single nucleotide variant	NM_001040108.2(MLH3):c.3344G>A (p.Arg1115Gln)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000472499]\|Endometrial carcinoma [RCV005398634]\|MLH3-related disorder [RCV003902650]\|not specified [RCV004022845]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75042414	75042414	Human	5	alternate_id
12890367	CV400267	single nucleotide variant	NM_001040108.2(MLH3):c.2911G>A (p.Val971Ile)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001118345]\|Endometrial carcinoma [RCV000763945]\|MLH3-related disorder [RCV003925324]\|not provided [RCV001356029]\|not specified [RCV003321615]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75046745	75046745	Human	3	alternate_id
12891340	CV400295	single nucleotide variant	NM_001040108.2(MLH3):c.359T>C (p.Phe120Ser)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000476413]\|Endometrial carcinoma [RCV005398671]\|MLH3-related disorder [RCV003915315]\|not provided [RCV003736785]\|not specified [RCV004023053]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75049297	75049297	Human	5	alternate_id
12887596	CV400487	single nucleotide variant	NM_001040108.2(MLH3):c.4185C>T (p.His1395=)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000469342]\|Endometrial carcinoma [RCV005355911]\|MLH3-related disorder [RCV003970356]\|not specified [RCV004023054]	likely benign	14	75018886	75018886	Human	3	alternate_id
13495359	CV463486	single nucleotide variant	NM_001040108.2(MLH3):c.2670G>A (p.Met890Ile)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000537080]\|MLH3-related disorder [RCV003952901]\|not specified [RCV003321671]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75046986	75046986	Human	1	alternate_id
13487666	CV464082	single nucleotide variant	NM_001040108.2(MLH3):c.3539G>A (p.Arg1180His)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000531935]\|Endometrial carcinoma [RCV005398872]\|MLH3-related disorder [RCV003952902]\|not specified [RCV002268174]	uncertain significance	14	75039942	75039942	Human	5	alternate_id
13496801	CV464493	single nucleotide variant	NM_001040108.2(MLH3):c.2356G>A (p.Val786Ile)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000560611]\|Endometrial carcinoma [RCV005398871]\|MLH3-related disorder [RCV003935563]\|not specified [RCV003493646]	likely benign\|uncertain significance	14	75047300	75047300	Human	5	alternate_id
13511814	CV485662	single nucleotide variant	NM_001040108.2(MLH3):c.2490T>G (p.Phe830Leu)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001119881]\|Endometrial carcinoma [RCV005392139]\|MLH3-related disorder [RCV003925753]\|not provided [RCV005231134]\|not specified [RCV000582902]	benign\|likely benign\|uncertain significance	14	75047166	75047166	Human	5	alternate_id
13626816	CV528274	single nucleotide variant	NM_001040108.2(MLH3):c.4186G>T (p.Gly1396Trp)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000655392]\|MLH3-related disorder [RCV004751652]\|not specified [RCV004025965]	uncertain significance	14	75018885	75018885	Human	1	alternate_id
13626809	CV528287	single nucleotide variant	NM_001040108.2(MLH3):c.3455G>A (p.Arg1152His)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000655385]\|Endometrial carcinoma [RCV005010635]\|MLH3-related disorder [RCV003403508]\|not provided [RCV003237980]\|not specified [RCV002268240]	uncertain significance	14	75041625	75041625	Human	5	alternate_id
13626819	CV528713	single nucleotide variant	NM_001040108.2(MLH3):c.4150C>G (p.Leu1384Val)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000655395]\|MLH3-related disorder [RCV003403509]\|not specified [RCV004025968]	uncertain significance	14	75018921	75018921	Human	1	alternate_id
13626825	CV528752	single nucleotide variant	NM_001040108.2(MLH3):c.1234A>G (p.Lys412Glu)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000655401]\|MLH3-related disorder [RCV003953213]\|not provided [RCV004792349]\|not specified [RCV002465746]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75048422	75048422	Human	1	alternate_id
13626813	CV528812	single nucleotide variant	NM_001040108.2(MLH3):c.3658G>A (p.Val1220Met)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000655389]\|Endometrial carcinoma [RCV005392249]\|MLH3-related disorder [RCV003392504]\|not specified [RCV004025962]	uncertain significance	14	75033476	75033476	Human	5	alternate_id
13626830	CV528828	single nucleotide variant	NM_001040108.2(MLH3):c.902A>T (p.Glu301Val)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000655407]\|Endometrial carcinoma [RCV005010636]\|MLH3-related disorder [RCV003965418]\|not specified [RCV004025972]	likely benign\|uncertain significance	14	75048754	75048754	Human	5	alternate_id
13812665	CV572913	single nucleotide variant	NM_001040108.2(MLH3):c.2435G>C (p.Ser812Thr)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000689604]\|MLH3-related disorder [RCV003392524]\|not specified [RCV002465754]	conflicting interpretations of pathogenicity\|uncertain significance	14	75047221	75047221	Human	1	alternate_id
13820502	CV572915	single nucleotide variant	NM_001040108.2(MLH3):c.1669G>A (p.Ala557Thr)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000694910]\|Endometrial carcinoma [RCV005010696]\|MLH3-related disorder [RCV003411617]\|not specified [RCV004025223]	uncertain significance	14	75047987	75047987	Human	5	alternate_id
14717711	CV642687	microsatellite	NM_001040108.2(MLH3):c.4150_4151del (p.Leu1384fs)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000795556]\|Endometrial carcinoma [RCV005392400]\|MLH3-related disorder [RCV003947985]\|not specified [RCV004027525]	uncertain significance	14	75018920	75018921	Human		alternate_id
14732204	CV642689	single nucleotide variant	NM_001040108.2(MLH3):c.3694C>T (p.Arg1232Cys)	Colorectal cancer [RCV005359585]\|Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000818189]\|MLH3-related disorder [RCV004751736]\|not specified [RCV004028946]	uncertain significance	14	75033440	75033440	Human	3	alternate_id
14732990	CV642711	single nucleotide variant	NM_001040108.2(MLH3):c.1724A>G (p.His575Arg)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000802098]\|MLH3-related disorder [RCV003411763]\|not specified [RCV004028090]	likely benign\|uncertain significance	14	75047932	75047932	Human	1	alternate_id
14721059	CV642720	single nucleotide variant	NM_001040108.2(MLH3):c.1082A>G (p.Asp361Gly)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000796929]\|MLH3-related disorder [RCV003396386]\|not specified [RCV003321736]	uncertain significance	14	75048574	75048574	Human	1	alternate_id
14738900	CV642722	single nucleotide variant	NM_001040108.2(MLH3):c.808T>G (p.Phe270Val)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000804723]\|MLH3-related disorder [RCV004751718]\|not specified [RCV004028192]	uncertain significance	14	75048848	75048848	Human	1	alternate_id
15129064	CV684526	single nucleotide variant	NM_001040108.2(MLH3):c.394G>A (p.Ala132Thr)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV000863177]\|MLH3-related disorder [RCV003938236]\|not specified [RCV002268339]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	75049262	75049262	Human	1	alternate_id
26890317	CV841728	single nucleotide variant	NM_001040108.2(MLH3):c.4268G>A (p.Arg1423His)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001059150]\|Endometrial carcinoma [RCV005012506]\|MLH3-related disorder [RCV003405269]\|not specified [RCV004031869]	uncertain significance	14	75017176	75017176	Human	5	alternate_id
26885759	CV841738	single nucleotide variant	NM_001040108.2(MLH3):c.3583G>A (p.Val1195Ile)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001054056]\|MLH3-related disorder [RCV004751866]	uncertain significance	14	75038400	75038400	Human	1	alternate_id
26903930	CV841750	single nucleotide variant	NM_001040108.2(MLH3):c.2129T>C (p.Leu710Ser)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001070078]\|MLH3-related disorder [RCV003396725]	uncertain significance	14	75047527	75047527	Human	1	alternate_id
26920785	CV841756	single nucleotide variant	NM_001040108.2(MLH3):c.1651C>T (p.Pro551Ser)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001048532]\|MLH3-related disorder [RCV003413842]\|not specified [RCV004031512]	likely benign\|uncertain significance	14	75048005	75048005	Human	1	alternate_id
38473905	CV927165	single nucleotide variant	NM_001040108.2(MLH3):c.2600A>G (p.Glu867Gly)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001214527]\|MLH3-related disorder [RCV003953584]\|not specified [RCV004033931]	uncertain significance	14	75047056	75047056	Human	1	alternate_id
38464097	CV957303	single nucleotide variant	NM_001040108.2(MLH3):c.958T>G (p.Cys320Gly)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001247345]\|Endometrial carcinoma [RCV005012683]\|MLH3-related disorder [RCV003973162]\|not specified [RCV002268461]	uncertain significance	14	75048698	75048698	Human	5	alternate_id
126760536	CV995961	single nucleotide variant	NM_001040108.2(MLH3):c.3406G>A (p.Glu1136Lys)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001309342]\|Endometrial carcinoma [RCV005012753]\|MLH3-related disorder [RCV003393968]\|Ovarian cancer [RCV003153983]\|not specified [RCV004034202]	benign\|uncertain significance	14	75041674	75041674	Human	7	alternate_id
126734162	CV995964	single nucleotide variant	NM_001040108.2(MLH3):c.3248C>A (p.Thr1083Lys)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV001304390]\|MLH3-related disorder [RCV003405521]\|not specified [RCV004036308]	uncertain significance	14	75046408	75046408	Human	1	alternate_id
150449325	CV1273618	deletion	NM_001040108.2(MLH3):c.3466-186_3466-174del	not provided [RCV001691718]	benign	14	75040189	75040201	Human		name
155799572	CV1859888	insertion	NM_001040108.2(MLH3):c.3570+27_3570+28insTAT	not specified [RCV002466132]	likely benign	14	75039883	75039884	Human		name
153303026	CV1690078	insertion	NM_001040108.2(MLH3):c.3570+27_3570+28insTATAT	not specified [RCV002268978]	likely benign	14	75039883	75039884	Human		name
401798304	CV2741384	microsatellite	NM_001040108.2(MLH3):c.3570+30_3570+31insATTATAT	not specified [RCV003322547]	likely benign	14	75039880	75039881	Human		name
153303024	CV1690077	insertion	NM_001040108.2(MLH3):c.3570+27_3570+28insTATATATAT	not specified [RCV002268977]	likely benign	14	75039883	75039884	Human		name
155799574	CV1859889	insertion	NM_001040108.2(MLH3):c.3570+27_3570+28insTATATATATAT	not specified [RCV002466133]	likely benign	14	75039883	75039884	Human		name
401795954	CV2740090	insertion	NM_001040108.2(MLH3):c.3570+27_3570+28insTATATATATATAT	not specified [RCV003320325]	benign	14	75039883	75039884	Human		name
405110083	CV3078752	single nucleotide variant	NM_001040108.2(MLH3):c.787A>T (p.Lys263Ter)	Colorectal cancer, hereditary nonpolyposis, type 7 [RCV003615412]	uncertain significance	14	75048869	75048869	Human	1	name
405702954	CV3388930	single nucleotide variant	NM_001040108.2(MLH3):c.738C>G (p.Asn246Lys)	not specified [RCV004521267]	uncertain significance	14	75048918	75048918	Human		name

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