Mast4 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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258 records found for search term Mast4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
153350052	CV1694084	single nucleotide variant	NM_001164664.2(MAST4):c.3526-3T>C	MAST4-associated generalized epilepsy [RCV002276489]	uncertain significance	5	67153455	67153455	Human		name , trait
15197423	CV730367	single nucleotide variant	NM_001164664.2(MAST4):c.1357-10T>C	not provided [RCV000890053]	likely benign	5	67110088	67110088	Human		name
8581174	CV115611	single nucleotide variant	NM_001164664.1(MAST4):c.363+8298G>C	Lung cancer [RCV000096134]	uncertain significance	5	66605316	66605316	Human		name
8581175	CV115612	single nucleotide variant	NM_001164664.1(MAST4):c.364-30479A>G	Lung cancer [RCV000096135]	uncertain significance	5	66729230	66729230	Human		name
152978401	CV1671584	single nucleotide variant	NM_001164664.2(MAST4):c.642+55458C>T	MAST-associated epilepsy syndrome [RCV002227689]	uncertain significance	5	66844252	66844252	Human		name
156096239	CV2399061	single nucleotide variant	NM_001164664.2(MAST4):c.642+40075G>A	not specified [RCV004245357]	uncertain significance	5	66828869	66828869	Human		name
616939973	CV4014303	single nucleotide variant	NM_001164664.2(MAST4):c.222C>G (p.Gly74=)	not provided [RCV005413797]	likely benign	5	66596877	66596877	Human		name
156156059	CV2388833	single nucleotide variant	NM_001164664.2(MAST4):c.40C>T (p.Arg14Cys)	not specified [RCV004239684]	uncertain significance	5	66596695	66596695	Human		name
401914923	CV2827794	single nucleotide variant	NM_001164664.2(MAST4):c.336C>T (p.Ser112=)	not provided [RCV003428529]	likely benign	5	66596991	66596991	Human		name
15179593	CV721502	single nucleotide variant	NM_001164664.2(MAST4):c.390C>T (p.Pro130=)	not provided [RCV000885326]	benign	5	66759735	66759735	Human		name
15178884	CV721503	single nucleotide variant	NM_001164664.2(MAST4):c.483G>A (p.Gln161=)	not provided [RCV000885164]	benign	5	66759828	66759828	Human		name
156083581	CV2330699	single nucleotide variant	NM_001164664.2(MAST4):c.101C>T (p.Pro34Leu)	not specified [RCV004185768]	uncertain significance	5	66596756	66596756	Human		name
15128667	CV709973	single nucleotide variant	NM_001164664.2(MAST4):c.2043G>A (p.Leu681=)	not provided [RCV000964124]	benign	5	67131901	67131901	Human		name
8631678	CV86882	single nucleotide variant	NM_001164664.1(MAST4):c.1995C>T (p.Leu665=)	Malignant melanoma [RCV000066973]	not provided	5	67131853	67131853	Human		name
150409861	CV1195996	single nucleotide variant	NM_001164664.2(MAST4):c.400C>T (p.Arg134Trp)	not provided [RCV001572822]	likely benign\|uncertain significance	5	66759745	66759745	Human		name
150548646	CV1294431	single nucleotide variant	NM_001164664.2(MAST4):c.7062A>G (p.Thr2354=)	not provided [RCV001751923]	benign	5	67166241	67166241	Human		name
156183292	CV2243258	single nucleotide variant	NM_001164664.2(MAST4):c.908T>G (p.Val303Gly)	not specified [RCV004110143]	uncertain significance	5	67095671	67095671	Human		name
156268809	CV2305806	single nucleotide variant	NM_001164664.2(MAST4):c.680G>A (p.Arg227Gln)	not specified [RCV004167610]	uncertain significance	5	67054409	67054409	Human		name
156396167	CV2326128	single nucleotide variant	NM_001164664.2(MAST4):c.695A>G (p.Lys232Arg)	not specified [RCV004180402]	uncertain significance	5	67054424	67054424	Human		name
156173569	CV2355188	single nucleotide variant	NM_001164664.2(MAST4):c.692G>A (p.Arg231Gln)	not specified [RCV004198569]	uncertain significance	5	67054421	67054421	Human		name
329396684	CV2455706	single nucleotide variant	NM_001164664.2(MAST4):c.978C>G (p.His326Gln)	not specified [RCV004279006]	uncertain significance	5	67100500	67100500	Human		name
401917708	CV2827795	single nucleotide variant	NM_001164664.2(MAST4):c.3036C>G (p.Ala1012=)	not provided [RCV003429658]	likely benign	5	67145321	67145321	Human		name
401917709	CV2827796	single nucleotide variant	NM_001164664.2(MAST4):c.3519C>T (p.Ile1173=)	not provided [RCV003429659]	likely benign	5	67152860	67152860	Human		name
401917711	CV2827798	single nucleotide variant	NM_001164664.2(MAST4):c.6759C>T (p.Thr2253=)	not provided [RCV003429660]	likely benign	5	67165938	67165938	Human		name
401917712	CV2827799	single nucleotide variant	NM_001164664.2(MAST4):c.7110A>G (p.Glu2370=)	not provided [RCV003429661]	likely benign	5	67166289	67166289	Human		name
401917715	CV2827801	single nucleotide variant	NM_001164664.2(MAST4):c.7659G>C (p.Val2553=)	not provided [RCV003429663]	likely benign	5	67166838	67166838	Human		name
405659096	CV3277985	single nucleotide variant	NM_001164664.2(MAST4):c.988A>G (p.Lys330Glu)	not specified [RCV004416660]	uncertain significance	5	67100510	67100510	Human		name
407472672	CV3456986	single nucleotide variant	NM_001164664.2(MAST4):c.689A>G (p.Asn230Ser)	not specified [RCV004637665]	uncertain significance	5	67054418	67054418	Human		name
597637077	CV3694288	single nucleotide variant	NM_001164664.2(MAST4):c.964C>G (p.Pro322Ala)	not specified [RCV004940927]	uncertain significance	5	67100486	67100486	Human		name
597637245	CV3694295	single nucleotide variant	NM_001164664.2(MAST4):c.734G>A (p.Arg245Gln)	not specified [RCV004940933]	uncertain significance	5	67054463	67054463	Human		name
597637267	CV3694299	single nucleotide variant	NM_001164664.2(MAST4):c.811G>T (p.Ala271Ser)	not specified [RCV004940937]	uncertain significance	5	67090209	67090209	Human		name
598199251	CV3981654	single nucleotide variant	NM_001164664.2(MAST4):c.758A>G (p.His253Arg)	not specified [RCV005375672]	uncertain significance	5	67054487	67054487	Human		name
598177215	CV3981658	single nucleotide variant	NM_001164664.2(MAST4):c.829C>T (p.Arg277Trp)	not specified [RCV005371560]	uncertain significance	5	67090227	67090227	Human		name
598199284	CV3981671	single nucleotide variant	NM_001164664.2(MAST4):c.998G>A (p.Cys333Tyr)	not specified [RCV005375677]	uncertain significance	5	67100520	67100520	Human		name
15181277	CV709974	single nucleotide variant	NM_001164664.2(MAST4):c.7074G>A (p.Pro2358=)	not provided [RCV000974353]	likely benign	5	67166253	67166253	Human		name
15136589	CV735159	single nucleotide variant	NM_001164664.2(MAST4):c.6468C>T (p.Ser2156=)	not provided [RCV000898654]	likely benign	5	67165647	67165647	Human		name
156163565	CV1866806	single nucleotide variant	NM_001164664.2(MAST4):c.2693T>C (p.Ile898Thr)	Infantile spasms [RCV002508178]	likely pathogenic	5	67142496	67142496	Human	2	name
156069336	CV2203778	single nucleotide variant	NM_001164664.2(MAST4):c.1742A>G (p.Tyr581Cys)	not specified [RCV004074420]	uncertain significance	5	67121099	67121099	Human		name
156379421	CV2207965	single nucleotide variant	NM_001164664.2(MAST4):c.2684A>G (p.Asn895Ser)	not specified [RCV004086341]	uncertain significance	5	67142487	67142487	Human		name
156328384	CV2216175	single nucleotide variant	NM_001164664.2(MAST4):c.1079G>A (p.Arg360His)	not specified [RCV004095627]	uncertain significance	5	67102544	67102544	Human		name
156181914	CV2222246	single nucleotide variant	NM_001164664.2(MAST4):c.1100A>G (p.His367Arg)	not specified [RCV004105270]	uncertain significance	5	67102565	67102565	Human		name
156141894	CV2288612	single nucleotide variant	NM_001164664.2(MAST4):c.2526C>G (p.Phe842Leu)	not specified [RCV004152129]	uncertain significance	5	67142146	67142146	Human		name
156185639	CV2292334	single nucleotide variant	NM_001164664.2(MAST4):c.1526G>T (p.Gly509Val)	not specified [RCV004150148]	uncertain significance	5	67114154	67114154	Human		name
156209528	CV2298214	single nucleotide variant	NM_001164664.2(MAST4):c.1360C>T (p.His454Tyr)	not specified [RCV004159862]	uncertain significance	5	67110101	67110101	Human		name
156064766	CV2316234	single nucleotide variant	NM_001164664.2(MAST4):c.1777C>T (p.Arg593Trp)	not specified [RCV004174268]	uncertain significance	5	67130241	67130241	Human		name
156265142	CV2329509	single nucleotide variant	NM_001164664.2(MAST4):c.1198C>A (p.Pro400Thr)	not specified [RCV004180643]	uncertain significance	5	67104417	67104417	Human		name
155916912	CV2366781	single nucleotide variant	NM_001164664.2(MAST4):c.2539G>A (p.Asp847Asn)	not specified [RCV004210773]	uncertain significance	5	67142159	67142159	Human		name
329354315	CV2437755	single nucleotide variant	NM_001164664.2(MAST4):c.1309C>G (p.Arg437Gly)	not specified [RCV004261058]	uncertain significance	5	67104528	67104528	Human		name
329373962	CV2452737	single nucleotide variant	NM_001164664.2(MAST4):c.1636C>A (p.Pro546Thr)	not specified [RCV004275284]	uncertain significance	5	67118726	67118726	Human		name
329373965	CV2452738	single nucleotide variant	NM_001164664.2(MAST4):c.1018A>G (p.Thr340Ala)	not specified [RCV004275285]	uncertain significance	5	67100540	67100540	Human		name
401879055	CV2778122	single nucleotide variant	NM_001164664.2(MAST4):c.1441C>T (p.Arg481Trp)	not specified [RCV004348064]	uncertain significance	5	67110182	67110182	Human		name
405659066	CV3277975	single nucleotide variant	NM_001164664.2(MAST4):c.1666A>G (p.Asn556Asp)	not specified [RCV004416650]	uncertain significance	5	67121023	67121023	Human		name
405659069	CV3277976	single nucleotide variant	NM_001164664.2(MAST4):c.1685G>A (p.Arg562Gln)	not specified [RCV004416651]	uncertain significance	5	67121042	67121042	Human		name
405659072	CV3277977	single nucleotide variant	NM_001164664.2(MAST4):c.1739C>G (p.Ala580Gly)	not specified [RCV004416652]	uncertain significance	5	67121096	67121096	Human		name
405659075	CV3277978	single nucleotide variant	NM_001164664.2(MAST4):c.2065A>G (p.Ile689Val)	not specified [RCV004416653]	uncertain significance	5	67131923	67131923	Human		name
405659078	CV3277979	single nucleotide variant	NM_001164664.2(MAST4):c.2119A>G (p.Ile707Val)	not specified [RCV004416654]	uncertain significance	5	67133539	67133539	Human		name
405659081	CV3277980	single nucleotide variant	NM_001164664.2(MAST4):c.2773G>A (p.Glu925Lys)	not specified [RCV004416655]	uncertain significance	5	67144711	67144711	Human		name
405659236	CV3278013	single nucleotide variant	NM_001164664.2(MAST4):c.1310G>A (p.Arg437Gln)	not specified [RCV004416688]	uncertain significance	5	67104529	67104529	Human		name
405659164	CV3278014	single nucleotide variant	NM_001164664.2(MAST4):c.1386G>T (p.Leu462Phe)	not specified [RCV004416689]	uncertain significance	5	67110127	67110127	Human		name
405659112	CV3278015	single nucleotide variant	NM_001164664.2(MAST4):c.1406T>C (p.Val469Ala)	not specified [RCV004416690]	uncertain significance	5	67110147	67110147	Human		name
407472663	CV3456984	single nucleotide variant	NM_001164664.2(MAST4):c.2897G>A (p.Ser966Asn)	not specified [RCV004637663]	uncertain significance	5	67145182	67145182	Human		name
407472682	CV3456988	single nucleotide variant	NM_001164664.2(MAST4):c.2465G>A (p.Arg822Lys)	not specified [RCV004637667]	uncertain significance	5	67136635	67136635	Human		name
407472694	CV3456993	single nucleotide variant	NM_001164664.2(MAST4):c.1691A>G (p.Lys564Arg)	not specified [RCV004637669]	uncertain significance	5	67121048	67121048	Human		name
597636964	CV3694265	single nucleotide variant	NM_001164664.2(MAST4):c.2398A>G (p.Ile800Val)	not specified [RCV004940906]	uncertain significance	5	67136568	67136568	Human		name
597636969	CV3694266	single nucleotide variant	NM_001164664.2(MAST4):c.2750G>A (p.Arg917Gln)	not specified [RCV004940907]	uncertain significance	5	67144688	67144688	Human		name
597636974	CV3694267	single nucleotide variant	NM_001164664.2(MAST4):c.2431C>T (p.Pro811Ser)	not specified [RCV004940908]	uncertain significance	5	67136601	67136601	Human		name
597637008	CV3694274	single nucleotide variant	NM_001164664.2(MAST4):c.2030C>T (p.Thr677Met)	not specified [RCV004940914]	uncertain significance	5	67131888	67131888	Human		name
597637018	CV3694276	single nucleotide variant	NM_001164664.2(MAST4):c.1078C>T (p.Arg360Cys)	not specified [RCV004940916]	uncertain significance	5	67102543	67102543	Human		name
597637029	CV3694278	single nucleotide variant	NM_001164664.2(MAST4):c.1587G>T (p.Leu529Phe)	not specified [RCV004940918]	uncertain significance	5	67114215	67114215	Human		name
597637061	CV3694285	single nucleotide variant	NM_001164664.2(MAST4):c.1646A>G (p.Asp549Gly)	not specified [RCV004940924]	uncertain significance	5	67118736	67118736	Human		name
597637217	CV3694289	single nucleotide variant	NM_001164664.2(MAST4):c.2395G>A (p.Glu799Lys)	not specified [RCV004940928]	uncertain significance	5	67136565	67136565	Human		name
597637228	CV3694292	single nucleotide variant	NM_001164664.2(MAST4):c.1611C>G (p.Asn537Lys)	not specified [RCV004940930]	uncertain significance	5	67118701	67118701	Human		name
597637250	CV3694296	single nucleotide variant	NM_001164664.2(MAST4):c.1367G>A (p.Arg456His)	not specified [RCV004940934]	uncertain significance	5	67110108	67110108	Human		name
597637256	CV3694297	single nucleotide variant	NM_001164664.2(MAST4):c.1334A>G (p.Lys445Arg)	not specified [RCV004940935]	uncertain significance	5	67104553	67104553	Human		name
597637293	CV3694305	single nucleotide variant	NM_001164664.2(MAST4):c.2726C>T (p.Ser909Leu)	not specified [RCV004940942]	uncertain significance	5	67142529	67142529	Human		name
598177204	CV3981655	single nucleotide variant	NM_001164664.2(MAST4):c.2873C>T (p.Thr958Ile)	not specified [RCV005371558]	uncertain significance	5	67145158	67145158	Human		name
598177241	CV3981662	single nucleotide variant	NM_001164664.2(MAST4):c.2398A>T (p.Ile800Phe)	not specified [RCV005371564]	uncertain significance	5	67136568	67136568	Human		name
598199279	CV3981666	single nucleotide variant	NM_001164664.2(MAST4):c.1268G>T (p.Arg423Leu)	not specified [RCV005375676]	uncertain significance	5	67104487	67104487	Human		name
598177265	CV3981669	single nucleotide variant	NM_001164664.2(MAST4):c.2504A>G (p.Tyr835Cys)	not specified [RCV005371568]	uncertain significance	5	67142124	67142124	Human		name
598177287	CV3981677	single nucleotide variant	NM_001164664.2(MAST4):c.1300A>G (p.Ile434Val)	not specified [RCV005371572]	uncertain significance	5	67104519	67104519	Human		name
598177292	CV3981678	single nucleotide variant	NM_001164664.2(MAST4):c.1508A>G (p.His503Arg)	not specified [RCV005371573]	uncertain significance	5	67114136	67114136	Human		name
598199314	CV3981679	single nucleotide variant	NM_001164664.2(MAST4):c.2220T>G (p.Asp740Glu)	not specified [RCV005375681]	uncertain significance	5	67133640	67133640	Human		name
598199323	CV3981684	single nucleotide variant	NM_001164664.2(MAST4):c.2742T>A (p.Ser914Arg)	not specified [RCV005375682]	uncertain significance	5	67144680	67144680	Human		name
598199332	CV3981686	single nucleotide variant	NM_001164664.2(MAST4):c.1778G>T (p.Arg593Leu)	not specified [RCV005375683]	uncertain significance	5	67130242	67130242	Human		name
8631676	CV86880	single nucleotide variant	NM_001164664.1(MAST4):c.1222G>A (p.Asp408Asn)	Malignant melanoma [RCV000066971]	not provided	5	67104441	67104441	Human		name
8631677	CV86881	single nucleotide variant	NM_001164664.1(MAST4):c.1465G>A (p.Asp489Asn)	Malignant melanoma [RCV000066972]	not provided	5	67114093	67114093	Human		name
156163583	CV1866807	single nucleotide variant	NM_001164664.2(MAST4):c.4412C>T (p.Thr1471Ile)	Infantile spasms [RCV002508179]	uncertain significance	5	67163591	67163591	Human	2	name
156163612	CV1866808	single nucleotide variant	NM_001164664.2(MAST4):c.7655C>G (p.Ser2552Trp)	Infantile spasms [RCV002508180]	likely pathogenic	5	67166834	67166834	Human	2	name
156134837	CV2196051	single nucleotide variant	NM_001164664.2(MAST4):c.6458G>A (p.Ser2153Asn)	not specified [RCV004072293]	uncertain significance	5	67165637	67165637	Human		name
156237502	CV2206899	single nucleotide variant	NM_001164664.2(MAST4):c.4408G>A (p.Val1470Met)	not specified [RCV004083567]	uncertain significance	5	67163587	67163587	Human		name
156108788	CV2211059	single nucleotide variant	NM_001164664.2(MAST4):c.5644G>A (p.Gly1882Ser)	not specified [RCV004088240]	uncertain significance	5	67164823	67164823	Human		name
155967105	CV2216796	single nucleotide variant	NM_001164664.2(MAST4):c.5153T>C (p.Leu1718Pro)	not specified [RCV004083233]	uncertain significance	5	67164332	67164332	Human		name
156332378	CV2218310	single nucleotide variant	NM_001164664.2(MAST4):c.5266G>A (p.Val1756Ile)	not specified [RCV004088495]	uncertain significance	5	67164445	67164445	Human		name
156185560	CV2222629	single nucleotide variant	NM_001164664.2(MAST4):c.3499A>T (p.Ile1167Phe)	not specified [RCV004099453]	uncertain significance	5	67152840	67152840	Human		name
156126993	CV2223735	single nucleotide variant	NM_001164664.2(MAST4):c.4930A>G (p.Thr1644Ala)	not specified [RCV004093821]	uncertain significance	5	67164109	67164109	Human		name
156291429	CV2226321	single nucleotide variant	NM_001164664.2(MAST4):c.5688C>G (p.Phe1896Leu)	not specified [RCV004099559]	likely benign	5	67164867	67164867	Human		name
156277718	CV2230833	single nucleotide variant	NM_001164664.2(MAST4):c.6800G>A (p.Gly2267Glu)	not specified [RCV004092047]	uncertain significance	5	67165979	67165979	Human		name
156253386	CV2232503	single nucleotide variant	NM_001164664.2(MAST4):c.7065C>G (p.Asp2355Glu)	not specified [RCV004099109]	uncertain significance	5	67166244	67166244	Human		name
156051404	CV2238004	single nucleotide variant	NM_001164664.2(MAST4):c.7630G>T (p.Ala2544Ser)	not specified [RCV004111037]	uncertain significance	5	67166809	67166809	Human		name
156055784	CV2243223	single nucleotide variant	NM_001164664.2(MAST4):c.4012A>G (p.Asn1338Asp)	not specified [RCV004110112]	uncertain significance	5	67163191	67163191	Human		name
155984410	CV2247759	single nucleotide variant	NM_001164664.2(MAST4):c.5167G>A (p.Val1723Ile)	not specified [RCV004121229]	uncertain significance	5	67164346	67164346	Human		name
155920067	CV2254984	single nucleotide variant	NM_001164664.2(MAST4):c.6851C>T (p.Ala2284Val)	not specified [RCV004117210]	uncertain significance	5	67166030	67166030	Human		name
156363923	CV2262732	single nucleotide variant	NM_001164664.2(MAST4):c.3596G>A (p.Gly1199Glu)	not specified [RCV004130917]	uncertain significance	5	67153528	67153528	Human		name
156058374	CV2262886	single nucleotide variant	NM_001164664.2(MAST4):c.5230A>G (p.Ser1744Gly)	not specified [RCV004125031]	uncertain significance	5	67164409	67164409	Human		name
155995472	CV2278086	single nucleotide variant	NM_001164664.2(MAST4):c.6560G>A (p.Ser2187Asn)	not specified [RCV004141304]	uncertain significance	5	67165739	67165739	Human		name
155955938	CV2281866	single nucleotide variant	NM_001164664.2(MAST4):c.4913G>A (p.Arg1638Gln)	not specified [RCV004136864]	uncertain significance	5	67164092	67164092	Human		name
156035695	CV2283001	single nucleotide variant	NM_001164664.2(MAST4):c.7232G>A (p.Gly2411Glu)	not specified [RCV004143628]	uncertain significance	5	67166411	67166411	Human		name
156293982	CV2293137	single nucleotide variant	NM_001164664.2(MAST4):c.6493G>A (p.Ala2165Thr)	not specified [RCV004150659]	uncertain significance	5	67165672	67165672	Human		name
155903678	CV2298661	single nucleotide variant	NM_001164664.2(MAST4):c.7444A>C (p.Thr2482Pro)	not specified [RCV004156239]	likely benign	5	67166623	67166623	Human		name
156153606	CV2303841	single nucleotide variant	NM_001164664.2(MAST4):c.7196G>A (p.Arg2399Gln)	not specified [RCV004168134]	uncertain significance	5	67166375	67166375	Human		name
156156773	CV2314405	single nucleotide variant	NM_001164664.2(MAST4):c.3425T>C (p.Ile1142Thr)	not specified [RCV004168523]	uncertain significance	5	67152766	67152766	Human		name
156070932	CV2318942	single nucleotide variant	NM_001164664.2(MAST4):c.5378G>A (p.Arg1793Lys)	not specified [RCV004175833]	uncertain significance	5	67164557	67164557	Human		name
156168344	CV2320078	single nucleotide variant	NM_001164664.2(MAST4):c.4625A>G (p.Asp1542Gly)	not specified [RCV004167929]	uncertain significance	5	67163804	67163804	Human		name
156272922	CV2323460	single nucleotide variant	NM_001164664.2(MAST4):c.6352G>A (p.Glu2118Lys)	not specified [RCV004165673]	uncertain significance	5	67165531	67165531	Human		name
156255839	CV2325795	single nucleotide variant	NM_001164664.2(MAST4):c.5719G>T (p.Ala1907Ser)	not specified [RCV004173681]	uncertain significance	5	67164898	67164898	Human		name
156183153	CV2327949	single nucleotide variant	NM_001164664.2(MAST4):c.3913T>G (p.Leu1305Val)	not specified [RCV004179265]	uncertain significance	5	67162734	67162734	Human		name
156396724	CV2330235	single nucleotide variant	NM_001164664.2(MAST4):c.6821C>T (p.Pro2274Leu)	not specified [RCV004187691]	uncertain significance	5	67166000	67166000	Human		name
156034821	CV2338802	single nucleotide variant	NM_001164664.2(MAST4):c.4227C>G (p.Ile1409Met)	not specified [RCV004182360]	uncertain significance	5	67163406	67163406	Human		name
155920044	CV2343279	single nucleotide variant	NM_001164664.2(MAST4):c.6190G>A (p.Ala2064Thr)	not specified [RCV004194900]	uncertain significance	5	67165369	67165369	Human		name
155928022	CV2349928	single nucleotide variant	NM_001164664.2(MAST4):c.5554G>C (p.Asp1852His)	not specified [RCV004206341]	uncertain significance	5	67164733	67164733	Human		name
156198284	CV2357838	single nucleotide variant	NM_001164664.2(MAST4):c.6437C>T (p.Pro2146Leu)	not specified [RCV004205122]	likely benign	5	67165616	67165616	Human		name
156105099	CV2361127	single nucleotide variant	NM_001164664.2(MAST4):c.3143G>A (p.Cys1048Tyr)	not specified [RCV004216317]	uncertain significance	5	67149437	67149437	Human		name
156160627	CV2361821	single nucleotide variant	NM_001164664.2(MAST4):c.6613A>G (p.Thr2205Ala)	not specified [RCV004223292]	uncertain significance	5	67165792	67165792	Human		name
155930236	CV2366634	single nucleotide variant	NM_001164664.2(MAST4):c.3299T>C (p.Met1100Thr)	not specified [RCV004210647]	uncertain significance	5	67152640	67152640	Human		name
156385186	CV2371726	single nucleotide variant	NM_001164664.2(MAST4):c.5462C>T (p.Pro1821Leu)	not specified [RCV004219007]	likely benign	5	67164641	67164641	Human		name
155937855	CV2373857	single nucleotide variant	NM_001164664.2(MAST4):c.6029A>C (p.Asp2010Ala)	not specified [RCV004224791]	uncertain significance	5	67165208	67165208	Human		name
155992650	CV2379335	single nucleotide variant	NM_001164664.2(MAST4):c.5498G>A (p.Gly1833Asp)	not specified [RCV004223796]	uncertain significance	5	67164677	67164677	Human		name
155938306	CV2380690	single nucleotide variant	NM_001164664.2(MAST4):c.3422C>T (p.Pro1141Leu)	not specified [RCV004218271]	uncertain significance	5	67152763	67152763	Human		name
155904031	CV2385393	single nucleotide variant	NM_001164664.2(MAST4):c.3368G>A (p.Arg1123Gln)	not specified [RCV004231042]	uncertain significance	5	67152709	67152709	Human		name
329373161	CV2439302	single nucleotide variant	NM_001164664.2(MAST4):c.7460C>A (p.Ala2487Asp)	not specified [RCV004249612]	uncertain significance	5	67166639	67166639	Human		name
329399124	CV2439463	single nucleotide variant	NM_001164664.2(MAST4):c.5852C>G (p.Ala1951Gly)	not specified [RCV004249750]	uncertain significance	5	67165031	67165031	Human		name
329398759	CV2442768	single nucleotide variant	NM_001164664.2(MAST4):c.3922C>G (p.Arg1308Gly)	not specified [RCV004251600]	uncertain significance	5	67162743	67162743	Human		name
329380191	CV2444257	single nucleotide variant	NM_001164664.2(MAST4):c.5968G>T (p.Ala1990Ser)	not specified [RCV004263025]	uncertain significance	5	67165147	67165147	Human		name
329389077	CV2448695	single nucleotide variant	NM_001164664.2(MAST4):c.4096G>A (p.Gly1366Arg)	not specified [RCV004259357]	uncertain significance	5	67163275	67163275	Human		name
329391321	CV2452238	single nucleotide variant	NM_001164664.2(MAST4):c.6917G>A (p.Arg2306Lys)	not specified [RCV004278933]	uncertain significance	5	67166096	67166096	Human		name
329398265	CV2464959	single nucleotide variant	NM_001164664.2(MAST4):c.6533A>G (p.Asp2178Gly)	not specified [RCV004284877]	uncertain significance	5	67165712	67165712	Human		name
329388360	CV2466296	single nucleotide variant	NM_001164664.2(MAST4):c.5666T>C (p.Val1889Ala)	not specified [RCV004280222]	likely benign	5	67164845	67164845	Human		name
401726758	CV2674532	single nucleotide variant	NM_001164664.2(MAST4):c.3833T>C (p.Leu1278Pro)	not specified [RCV004291411]	uncertain significance	5	67162654	67162654	Human		name
401741960	CV2677477	single nucleotide variant	NM_001164664.2(MAST4):c.6842C>T (p.Pro2281Leu)	not specified [RCV004289546]	uncertain significance	5	67166021	67166021	Human		name
401736925	CV2679183	single nucleotide variant	NM_001164664.2(MAST4):c.4555G>A (p.Gly1519Ser)	not specified [RCV004285743]	uncertain significance	5	67163734	67163734	Human		name
401741342	CV2680385	single nucleotide variant	NM_001164664.2(MAST4):c.4835G>A (p.Ser1612Asn)	not specified [RCV004288631]	uncertain significance	5	67164014	67164014	Human		name
401741347	CV2680386	single nucleotide variant	NM_001164664.2(MAST4):c.4836C>A (p.Ser1612Arg)	not specified [RCV004288632]	uncertain significance	5	67164015	67164015	Human		name
401722056	CV2680802	single nucleotide variant	NM_001164664.2(MAST4):c.3566A>G (p.Lys1189Arg)	not specified [RCV004293451]	uncertain significance	5	67153498	67153498	Human		name
401753485	CV2684956	single nucleotide variant	NM_001164664.2(MAST4):c.6632C>G (p.Ser2211Cys)	not specified [RCV004296455]	uncertain significance	5	67165811	67165811	Human		name
401745071	CV2693173	single nucleotide variant	NM_001164664.2(MAST4):c.7469G>A (p.Gly2490Asp)	not specified [RCV004293106]	uncertain significance	5	67166648	67166648	Human		name
401773083	CV2698087	single nucleotide variant	NM_001164664.2(MAST4):c.3187G>A (p.Ala1063Thr)	not specified [RCV004302884]	uncertain significance	5	67149481	67149481	Human		name
401776544	CV2703274	single nucleotide variant	NM_001164664.2(MAST4):c.7423G>A (p.Ala2475Thr)	not specified [RCV004315635]	uncertain significance	5	67166602	67166602	Human		name
401758860	CV2705194	single nucleotide variant	NM_001164664.2(MAST4):c.6576C>G (p.His2192Gln)	not specified [RCV004310079]	uncertain significance	5	67165755	67165755	Human		name
401720358	CV2705851	single nucleotide variant	NM_001164664.2(MAST4):c.4464C>A (p.Ser1488Arg)	not specified [RCV004320466]	uncertain significance	5	67163643	67163643	Human		name
401777053	CV2707683	single nucleotide variant	NM_001164664.2(MAST4):c.4803C>A (p.Ser1601Arg)	not specified [RCV004306943]	uncertain significance	5	67163982	67163982	Human		name
401889960	CV2762026	single nucleotide variant	NM_001164664.2(MAST4):c.5272C>T (p.Leu1758Phe)	not specified [RCV004341847]	uncertain significance	5	67164451	67164451	Human		name
401880155	CV2766143	single nucleotide variant	NM_001164664.2(MAST4):c.6899A>G (p.Lys2300Arg)	not specified [RCV004340594]	uncertain significance	5	67166078	67166078	Human		name
401859963	CV2768421	single nucleotide variant	NM_001164664.2(MAST4):c.6386A>C (p.His2129Pro)	not specified [RCV004344313]	uncertain significance	5	67165565	67165565	Human		name
401880144	CV2769943	single nucleotide variant	NM_001164664.2(MAST4):c.6597C>G (p.Asp2199Glu)	not specified [RCV004353780]	uncertain significance	5	67165776	67165776	Human		name
401860591	CV2776108	single nucleotide variant	NM_001164664.2(MAST4):c.7226G>A (p.Gly2409Glu)	not specified [RCV004353210]	uncertain significance	5	67166405	67166405	Human		name
401884573	CV2789723	single nucleotide variant	NM_001164664.2(MAST4):c.5567C>T (p.Ala1856Val)	not specified [RCV004361844]	uncertain significance	5	67164746	67164746	Human		name
401914925	CV2827797	single nucleotide variant	NM_001164664.2(MAST4):c.3545C>T (p.Pro1182Leu)	not provided [RCV003428530]	likely benign	5	67153477	67153477	Human		name
405659084	CV3277981	single nucleotide variant	NM_001164664.2(MAST4):c.3218G>C (p.Ser1073Thr)	not specified [RCV004416656]	uncertain significance	5	67149512	67149512	Human		name
405659090	CV3277983	single nucleotide variant	NM_001164664.2(MAST4):c.4071A>T (p.Lys1357Asn)	not specified [RCV004416658]	uncertain significance	5	67163250	67163250	Human		name
405659094	CV3277984	single nucleotide variant	NM_001164664.2(MAST4):c.4582G>A (p.Asp1528Asn)	not specified [RCV004416659]	uncertain significance	5	67163761	67163761	Human		name
405659104	CV3277988	single nucleotide variant	NM_001164664.2(MAST4):c.5803C>G (p.Pro1935Ala)	not specified [RCV004416663]	uncertain significance	5	67164982	67164982	Human		name
405659107	CV3277989	single nucleotide variant	NM_001164664.2(MAST4):c.5857C>A (p.Pro1953Thr)	not specified [RCV004416664]	uncertain significance	5	67165036	67165036	Human		name
405659110	CV3277990	single nucleotide variant	NM_001164664.2(MAST4):c.5864G>A (p.Cys1955Tyr)	not specified [RCV004416665]	uncertain significance	5	67165043	67165043	Human		name
405659469	CV3277991	single nucleotide variant	NM_001164664.2(MAST4):c.5960C>A (p.Ala1987Asp)	not specified [RCV004416666]	uncertain significance	5	67165139	67165139	Human		name
405659466	CV3277992	single nucleotide variant	NM_001164664.2(MAST4):c.6248C>G (p.Pro2083Arg)	not specified [RCV004416667]	uncertain significance	5	67165427	67165427	Human		name
405659463	CV3277993	single nucleotide variant	NM_001164664.2(MAST4):c.6298G>C (p.Glu2100Gln)	not specified [RCV004416668]	uncertain significance	5	67165477	67165477	Human		name
405659460	CV3277994	single nucleotide variant	NM_001164664.2(MAST4):c.6304A>C (p.Ser2102Arg)	not specified [RCV004416669]	uncertain significance	5	67165483	67165483	Human		name
405659458	CV3277995	single nucleotide variant	NM_001164664.2(MAST4):c.6526C>G (p.Pro2176Ala)	not specified [RCV004416670]	uncertain significance	5	67165705	67165705	Human		name
405659455	CV3277996	single nucleotide variant	NM_001164664.2(MAST4):c.6734G>A (p.Ser2245Asn)	not specified [RCV004416671]	uncertain significance	5	67165913	67165913	Human		name
405659453	CV3277997	single nucleotide variant	NM_001164664.2(MAST4):c.6769C>A (p.Gln2257Lys)	not specified [RCV004416672]	uncertain significance	5	67165948	67165948	Human		name
405659450	CV3277998	single nucleotide variant	NM_001164664.2(MAST4):c.6772A>G (p.Asn2258Asp)	not specified [RCV004416673]	uncertain significance	5	67165951	67165951	Human		name
405659448	CV3277999	single nucleotide variant	NM_001164664.2(MAST4):c.6848A>G (p.Asp2283Gly)	not specified [RCV004416674]	uncertain significance	5	67166027	67166027	Human		name
405659445	CV3278000	single nucleotide variant	NM_001164664.2(MAST4):c.6947C>A (p.Ala2316Glu)	not specified [RCV004416675]	uncertain significance	5	67166126	67166126	Human		name
405659442	CV3278001	single nucleotide variant	NM_001164664.2(MAST4):c.7073C>T (p.Pro2358Leu)	not specified [RCV004416676]	likely benign	5	67166252	67166252	Human		name
405659439	CV3278002	single nucleotide variant	NM_001164664.2(MAST4):c.7096G>A (p.Asp2366Asn)	not specified [RCV004416677]	uncertain significance	5	67166275	67166275	Human		name
405659436	CV3278003	single nucleotide variant	NM_001164664.2(MAST4):c.7112G>A (p.Gly2371Glu)	not specified [RCV004416678]	uncertain significance	5	67166291	67166291	Human		name
405659434	CV3278004	single nucleotide variant	NM_001164664.2(MAST4):c.7123A>G (p.Thr2375Ala)	not specified [RCV004416679]	uncertain significance	5	67166302	67166302	Human		name
405659431	CV3278005	single nucleotide variant	NM_001164664.2(MAST4):c.7199T>G (p.Leu2400Trp)	not specified [RCV004416680]	uncertain significance	5	67166378	67166378	Human		name
405659428	CV3278006	single nucleotide variant	NM_001164664.2(MAST4):c.7304A>G (p.Asn2435Ser)	not specified [RCV004416681]	likely benign	5	67166483	67166483	Human		name
405659426	CV3278007	single nucleotide variant	NM_001164664.2(MAST4):c.7553G>A (p.Ser2518Asn)	not specified [RCV004416682]	uncertain significance	5	67166732	67166732	Human		name
405659423	CV3278008	single nucleotide variant	NM_001164664.2(MAST4):c.7655C>T (p.Ser2552Leu)	not specified [RCV004416683]	uncertain significance	5	67166834	67166834	Human		name
405659419	CV3278009	single nucleotide variant	NM_001164664.2(MAST4):c.7661C>T (p.Thr2554Ile)	not specified [RCV004416684]	uncertain significance	5	67166840	67166840	Human		name
405659417	CV3278010	single nucleotide variant	NM_001164664.2(MAST4):c.7729A>G (p.Asn2577Asp)	not specified [RCV004416685]	uncertain significance	5	67166908	67166908	Human		name
405659414	CV3278011	single nucleotide variant	NM_001164664.2(MAST4):c.7780C>T (p.Pro2594Ser)	not specified [RCV004416686]	uncertain significance	5	67166959	67166959	Human		name
405659318	CV3278012	single nucleotide variant	NM_001164664.2(MAST4):c.7850G>A (p.Ser2617Asn)	not specified [RCV004416687]	uncertain significance	5	67167029	67167029	Human		name
407472621	CV3456973	single nucleotide variant	NM_001164664.2(MAST4):c.5807A>G (p.Lys1936Arg)	not specified [RCV004637654]	uncertain significance	5	67164986	67164986	Human		name
407472626	CV3456974	single nucleotide variant	NM_001164664.2(MAST4):c.4912C>T (p.Arg1638Trp)	not specified [RCV004637655]	uncertain significance	5	67164091	67164091	Human		name
407472632	CV3456975	single nucleotide variant	NM_001164664.2(MAST4):c.6175T>A (p.Ser2059Thr)	not specified [RCV004637656]	uncertain significance	5	67165354	67165354	Human		name
407472638	CV3456976	single nucleotide variant	NM_001164664.2(MAST4):c.6176C>A (p.Ser2059Tyr)	not specified [RCV004637657]	uncertain significance	5	67165355	67165355	Human		name
407469325	CV3456977	single nucleotide variant	NM_001164664.2(MAST4):c.3149A>G (p.Asp1050Gly)	not specified [RCV004636586]	uncertain significance	5	67149443	67149443	Human		name
407469328	CV3456978	single nucleotide variant	NM_001164664.2(MAST4):c.5564G>C (p.Ser1855Thr)	not specified [RCV004636587]	uncertain significance	5	67164743	67164743	Human		name
407472642	CV3456979	single nucleotide variant	NM_001164664.2(MAST4):c.6172A>G (p.Asn2058Asp)	not specified [RCV004637658]	likely benign	5	67165351	67165351	Human		name
407472646	CV3456980	single nucleotide variant	NM_001164664.2(MAST4):c.6530A>G (p.Gln2177Arg)	not specified [RCV004637659]	uncertain significance	5	67165709	67165709	Human		name
407472649	CV3456981	single nucleotide variant	NM_001164664.2(MAST4):c.5327C>G (p.Ala1776Gly)	not specified [RCV004637660]	uncertain significance	5	67164506	67164506	Human		name
407472652	CV3456982	single nucleotide variant	NM_001164664.2(MAST4):c.5198C>T (p.Pro1733Leu)	not specified [RCV004637661]	uncertain significance	5	67164377	67164377	Human		name
407472668	CV3456985	single nucleotide variant	NM_001164664.2(MAST4):c.7184A>G (p.His2395Arg)	not specified [RCV004637664]	uncertain significance	5	67166363	67166363	Human		name
407472677	CV3456987	single nucleotide variant	NM_001164664.2(MAST4):c.5171G>T (p.Arg1724Leu)	not specified [RCV004637666]	uncertain significance	5	67164350	67164350	Human		name
407469331	CV3456989	single nucleotide variant	NM_001164664.2(MAST4):c.7115A>G (p.Lys2372Arg)	not specified [RCV004636588]	uncertain significance	5	67166294	67166294	Human		name
407472688	CV3456990	single nucleotide variant	NM_001164664.2(MAST4):c.7168G>A (p.Gly2390Ser)	not specified [RCV004637668]	likely benign	5	67166347	67166347	Human		name
407469334	CV3456991	single nucleotide variant	NM_001164664.2(MAST4):c.3020C>G (p.Pro1007Arg)	not specified [RCV004636589]	uncertain significance	5	67145305	67145305	Human		name
407469337	CV3456992	single nucleotide variant	NM_001164664.2(MAST4):c.5338C>T (p.Pro1780Ser)	not specified [RCV004636590]	uncertain significance	5	67164517	67164517	Human		name
597636942	CV3694261	single nucleotide variant	NM_001164664.2(MAST4):c.4919C>T (p.Pro1640Leu)	not specified [RCV004940902]	uncertain significance	5	67164098	67164098	Human		name
597636947	CV3694262	single nucleotide variant	NM_001164664.2(MAST4):c.6404C>T (p.Pro2135Leu)	not specified [RCV004940903]	uncertain significance	5	67165583	67165583	Human		name
597636953	CV3694263	single nucleotide variant	NM_001164664.2(MAST4):c.3328A>G (p.Met1110Val)	not specified [RCV004940904]	uncertain significance	5	67152669	67152669	Human		name
597636958	CV3694264	single nucleotide variant	NM_001164664.2(MAST4):c.7124C>T (p.Thr2375Ile)	not specified [RCV004940905]	uncertain significance	5	67166303	67166303	Human		name
597636980	CV3694268	single nucleotide variant	NM_001164664.2(MAST4):c.6354A>T (p.Glu2118Asp)	not specified [RCV004940909]	uncertain significance	5	67165533	67165533	Human		name
597636985	CV3694270	single nucleotide variant	NM_001164664.2(MAST4):c.7694C>G (p.Pro2565Arg)	not specified [RCV004940910]	uncertain significance	5	67166873	67166873	Human		name
597636992	CV3694271	single nucleotide variant	NM_001164664.2(MAST4):c.5476G>A (p.Ala1826Thr)	not specified [RCV004940911]	uncertain significance	5	67164655	67164655	Human		name
597636997	CV3694272	single nucleotide variant	NM_001164664.2(MAST4):c.6218G>A (p.Gly2073Asp)	not specified [RCV004940912]	uncertain significance	5	67165397	67165397	Human		name
597637003	CV3694273	single nucleotide variant	NM_001164664.2(MAST4):c.3550T>G (p.Cys1184Gly)	not specified [RCV004940913]	uncertain significance	5	67153482	67153482	Human		name
597637012	CV3694275	single nucleotide variant	NM_001164664.2(MAST4):c.6543G>T (p.Lys2181Asn)	not specified [RCV004940915]	uncertain significance	5	67165722	67165722	Human		name
597637023	CV3694277	single nucleotide variant	NM_001164664.2(MAST4):c.4534C>T (p.Arg1512Cys)	not specified [RCV004940917]	uncertain significance	5	67163713	67163713	Human		name
597637034	CV3694280	single nucleotide variant	NM_001164664.2(MAST4):c.4931C>G (p.Thr1644Ser)	not specified [RCV004940919]	uncertain significance	5	67164110	67164110	Human		name
597637040	CV3694281	single nucleotide variant	NM_001164664.2(MAST4):c.6883C>G (p.Leu2295Val)	not specified [RCV004940920]	uncertain significance	5	67166062	67166062	Human		name
597637045	CV3694282	single nucleotide variant	NM_001164664.2(MAST4):c.7759C>T (p.Pro2587Ser)	not specified [RCV004940921]	uncertain significance	5	67166938	67166938	Human		name
597637050	CV3694283	single nucleotide variant	NM_001164664.2(MAST4):c.5921C>G (p.Ser1974Cys)	not specified [RCV004940922]	uncertain significance	5	67165100	67165100	Human		name
597637055	CV3694284	single nucleotide variant	NM_001164664.2(MAST4):c.7589C>T (p.Pro2530Leu)	not specified [RCV004940923]	uncertain significance	5	67166768	67166768	Human		name
597637066	CV3694286	single nucleotide variant	NM_001164664.2(MAST4):c.5058C>G (p.Ile1686Met)	not specified [RCV004940925]	uncertain significance	5	67164237	67164237	Human		name
597637072	CV3694287	single nucleotide variant	NM_001164664.2(MAST4):c.7816C>G (p.Arg2606Gly)	not specified [RCV004940926]	uncertain significance	5	67166995	67166995	Human		name
597637222	CV3694291	single nucleotide variant	NM_001164664.2(MAST4):c.5467C>G (p.Pro1823Ala)	not specified [RCV004940929]	uncertain significance	5	67164646	67164646	Human		name
597637233	CV3694293	single nucleotide variant	NM_001164664.2(MAST4):c.7385C>G (p.Ser2462Cys)	not specified [RCV004940931]	uncertain significance	5	67166564	67166564	Human		name
597637239	CV3694294	single nucleotide variant	NM_001164664.2(MAST4):c.7270C>T (p.Pro2424Ser)	not specified [RCV004940932]	uncertain significance	5	67166449	67166449	Human		name
597637262	CV3694298	single nucleotide variant	NM_001164664.2(MAST4):c.7744G>A (p.Val2582Met)	not specified [RCV004940936]	uncertain significance	5	67166923	67166923	Human		name
597637272	CV3694300	single nucleotide variant	NM_001164664.2(MAST4):c.4612G>C (p.Val1538Leu)	not specified [RCV004940938]	uncertain significance	5	67163791	67163791	Human		name
597637282	CV3694303	single nucleotide variant	NM_001164664.2(MAST4):c.7296C>G (p.Asp2432Glu)	not specified [RCV004940940]	uncertain significance	5	67166475	67166475	Human		name
597637288	CV3694304	single nucleotide variant	NM_001164664.2(MAST4):c.4697T>A (p.Leu1566Gln)	not specified [RCV004940941]	uncertain significance	5	67163876	67163876	Human		name
597636928	CV3697753	single nucleotide variant	NM_001164664.2(MAST4):c.4537C>T (p.Pro1513Ser)	not specified [RCV004940900]	uncertain significance	5	67163716	67163716	Human		name
597636934	CV3697754	single nucleotide variant	NM_001164664.2(MAST4):c.5867C>T (p.Pro1956Leu)	not specified [RCV004940901]	likely benign	5	67165046	67165046	Human		name
598221940	CV3893808	single nucleotide variant	NM_001164664.2(MAST4):c.7487C>A (p.Ala2496Asp)	not provided [RCV005257051]	likely benign	5	67166666	67166666	Human		name
598177192	CV3981652	single nucleotide variant	NM_001164664.2(MAST4):c.7087G>A (p.Ala2363Thr)	not specified [RCV005371556]	likely benign	5	67166266	67166266	Human		name
598177199	CV3981653	single nucleotide variant	NM_001164664.2(MAST4):c.7816C>T (p.Arg2606Trp)	not specified [RCV005371557]	uncertain significance	5	67166995	67166995	Human		name
598199258	CV3981657	single nucleotide variant	NM_001164664.2(MAST4):c.6254C>T (p.Ala2085Val)	not specified [RCV005375673]	uncertain significance	5	67165433	67165433	Human		name
598177223	CV3981659	single nucleotide variant	NM_001164664.2(MAST4):c.5592A>C (p.Leu1864Phe)	not specified [RCV005371561]	likely benign	5	67164771	67164771	Human		name
598177229	CV3981660	single nucleotide variant	NM_001164664.2(MAST4):c.5816C>A (p.Thr1939Asn)	not specified [RCV005371562]	uncertain significance	5	67164995	67164995	Human		name
598177236	CV3981661	single nucleotide variant	NM_001164664.2(MAST4):c.6914C>T (p.Pro2305Leu)	not specified [RCV005371563]	uncertain significance	5	67166093	67166093	Human		name
598199266	CV3981663	single nucleotide variant	NM_001164664.2(MAST4):c.7633A>G (p.Ser2545Gly)	not specified [RCV005375674]	likely benign	5	67166812	67166812	Human		name
598199272	CV3981665	single nucleotide variant	NM_001164664.2(MAST4):c.4181G>A (p.Arg1394Gln)	not specified [RCV005375675]	uncertain significance	5	67163360	67163360	Human		name
598177253	CV3981667	single nucleotide variant	NM_001164664.2(MAST4):c.5857C>T (p.Pro1953Ser)	not specified [RCV005371566]	uncertain significance	5	67165036	67165036	Human		name
598177259	CV3981668	single nucleotide variant	NM_001164664.2(MAST4):c.4445G>A (p.Arg1482Gln)	not specified [RCV005371567]	uncertain significance	5	67163624	67163624	Human		name
598177271	CV3981670	single nucleotide variant	NM_001164664.2(MAST4):c.7732G>C (p.Val2578Leu)	not specified [RCV005371569]	uncertain significance	5	67166911	67166911	Human		name
598199292	CV3981672	single nucleotide variant	NM_001164664.2(MAST4):c.5621C>T (p.Pro1874Leu)	not specified [RCV005375678]	uncertain significance	5	67164800	67164800	Human		name
598177276	CV3981673	single nucleotide variant	NM_001164664.2(MAST4):c.6695T>C (p.Leu2232Pro)	not specified [RCV005371570]	likely benign	5	67165874	67165874	Human		name
598199299	CV3981674	single nucleotide variant	NM_001164664.2(MAST4):c.5528T>C (p.Leu1843Pro)	not specified [RCV005375679]	uncertain significance	5	67164707	67164707	Human		name
598199307	CV3981676	single nucleotide variant	NM_001164664.2(MAST4):c.6052G>A (p.Val2018Met)	not specified [RCV005375680]	uncertain significance	5	67165231	67165231	Human		name
598177298	CV3981680	single nucleotide variant	NM_001164664.2(MAST4):c.4824C>A (p.His1608Gln)	not specified [RCV005371574]	uncertain significance	5	67164003	67164003	Human		name
598177304	CV3981681	single nucleotide variant	NM_001164664.2(MAST4):c.4705C>G (p.Leu1569Val)	not specified [RCV005371575]	uncertain significance	5	67163884	67163884	Human		name
598177311	CV3981682	single nucleotide variant	NM_001164664.2(MAST4):c.7487C>G (p.Ala2496Gly)	not specified [RCV005371576]	uncertain significance	5	67166666	67166666	Human		name
598177318	CV3981683	single nucleotide variant	NM_001164664.2(MAST4):c.3445A>G (p.Lys1149Glu)	not specified [RCV005371577]	uncertain significance	5	67152786	67152786	Human		name
598177324	CV3981685	single nucleotide variant	NM_001164664.2(MAST4):c.7525G>T (p.Gly2509Trp)	not specified [RCV005371578]	uncertain significance	5	67166704	67166704	Human		name
617152313	CV4020681	single nucleotide variant	NM_001164664.2(MAST4):c.5345G>A (p.Arg1782Lys)	not provided [RCV005427938]	likely benign	5	67164524	67164524	Human		name
15099651	CV699145	single nucleotide variant	NM_001164664.2(MAST4):c.3391T>A (p.Ser1131Thr)	not provided [RCV000958793]	benign	5	67152732	67152732	Human		name
15175842	CV699146	single nucleotide variant	NM_001164664.2(MAST4):c.6384G>C (p.Arg2128Ser)	not provided [RCV000950683]	benign	5	67165563	67165563	Human		name
15175846	CV699147	single nucleotide variant	NM_001164664.2(MAST4):c.7136A>G (p.Tyr2379Cys)	not provided [RCV000950684]	benign	5	67166315	67166315	Human		name
15167355	CV721504	single nucleotide variant	NM_001164664.2(MAST4):c.4237T>C (p.Phe1413Leu)	not provided [RCV000882830]	likely benign	5	67163416	67163416	Human		name
8631679	CV86883	single nucleotide variant	NM_001164664.1(MAST4):c.3019C>T (p.Pro1007Ser)	Malignant melanoma [RCV000066974]	not provided	5	67145304	67145304	Human		name
40815138	CV970272	single nucleotide variant	NM_001164664.2(MAST4):c.3475C>T (p.Arg1159Trp)	Moyamoya angiopathy [RCV004704507]	likely pathogenic	5	67152816	67152816	Human		name
598128755	CV3886552	microsatellite	NM_001164664.2(MAST4):c.6043CTC[1] (p.Leu2016del)	not provided [RCV005244212]	likely benign	5	67165222	67165224	Human		name
401917714	CV2827800	microsatellite	NM_001164664.2(MAST4):c.7419_7422del (p.Glu2474fs)	not provided [RCV003429662]	uncertain significance	5	67166596	67166599	Human		name

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