Homer2 Variant Search Result - Rat Genome Database

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184 records found for search term Homer2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405007196	CV2926695	single nucleotide variant	NM_004839.4(HOMER2):c.6-8T>C	not provided [RCV003576431]	likely benign	15	82892849	82892849	Human		name
13535322	CV505429	single nucleotide variant	NM_004839.4(HOMER2):c.6-4G>C	not provided [RCV000992157]\|not specified [RCV000602260]	benign	15	82892845	82892845	Human		name
150511963	CV1212881	single nucleotide variant	NM_004839.4(HOMER2):c.5+94G>T	not provided [RCV001598113]	benign	15	82952437	82952437	Human		name
150472508	CV1217192	single nucleotide variant	NM_004839.4(HOMER2):c.6-13T>C	not provided [RCV001615487]	benign	15	82892854	82892854	Human		name
150460512	CV1253118	single nucleotide variant	NM_004839.4(HOMER2):c.5+62C>G	not provided [RCV001669447]	benign	15	82952469	82952469	Human		name
150531414	CV1310847	single nucleotide variant	NM_004839.4(HOMER2):c.*172C>T	not provided [RCV001776581]	likely benign	15	82849543	82849543	Human		name
405037658	CV3130923	single nucleotide variant	NM_004839.4(HOMER2):c.6-19G>A	not provided [RCV003831141]	likely benign	15	82892860	82892860	Human		name
597925298	CV3748584	single nucleotide variant	NM_004839.4(HOMER2):c.5+15G>A	not provided [RCV005075232]	likely benign	15	82952516	82952516	Human		name
150437447	CV1249870	single nucleotide variant	NM_004839.4(HOMER2):c.5+145G>A	not provided [RCV001665784]	benign	15	82952386	82952386	Human		name
156017464	CV2121488	single nucleotide variant	NM_004839.4(HOMER2):c.494+4A>G	not provided [RCV002948609]	uncertain significance	15	82859025	82859025	Human		name
156096792	CV2152196	single nucleotide variant	NM_004839.4(HOMER2):c.162+4C>T	not provided [RCV003020897]	uncertain significance	15	82892681	82892681	Human		name
405238446	CV2891404	single nucleotide variant	NM_004839.4(HOMER2):c.163-8T>G	not provided [RCV003556866]	likely benign	15	82875412	82875412	Human		name
405243403	CV3071855	single nucleotide variant	NM_004839.4(HOMER2):c.387+7C>T	not provided [RCV003737791]	benign	15	82864160	82864160	Human		name
405237693	CV3077726	single nucleotide variant	NM_004839.4(HOMER2):c.762+2T>A	not provided [RCV003736213]	likely benign	15	82852140	82852140	Human		name
405286624	CV3192863	single nucleotide variant	NM_004839.4(HOMER2):c.843+9G>A	HOMER2-related disorder [RCV003981581]	likely benign	15	82851142	82851142	Human		name , trait , alternate_id
597940530	CV3757256	duplication	NM_004839.4(HOMER2):c.763-8dup	not provided [RCV005077441]	benign	15	82851238	82851239	Human		name
13539254	CV505215	single nucleotide variant	NM_004839.4(HOMER2):c.651+9G>A	not provided [RCV002063046]\|not specified [RCV000613026]	benign	15	82854635	82854635	Human		name
13537979	CV505851	single nucleotide variant	NM_004839.4(HOMER2):c.387+6A>T	HOMER2-related disorder [RCV003917908]\|not provided [RCV000992156]\|not specified [RCV000611167]	benign	15	82864161	82864161	Human	1	name , trait , alternate_id
13834401	CV585647	deletion	NM_004839.4(HOMER2):c.763-8del	not provided [RCV000729910]	conflicting interpretations of pathogenicity\|uncertain significance	15	82851239	82851239	Human		name
150330788	CV1172779	single nucleotide variant	NM_004839.4(HOMER2):c.163-21C>T	not provided [RCV001538279]	benign	15	82875425	82875425	Human		name
150431030	CV1235311	single nucleotide variant	NM_004839.4(HOMER2):c.294+67G>A	not provided [RCV001641681]	benign	15	82875206	82875206	Human		name
150464881	CV1252787	single nucleotide variant	NM_004839.4(HOMER2):c.388-25G>A	HOMER2-related disorder [RCV003941064]\|not provided [RCV001670111]	benign	15	82859160	82859160	Human	1	name , trait , alternate_id
150506737	CV1258040	single nucleotide variant	NM_004839.4(HOMER2):c.652-32G>A	not provided [RCV001678257]	benign	15	82852284	82852284	Human		name
150444992	CV1261127	single nucleotide variant	NM_004839.4(HOMER2):c.388-61A>G	not provided [RCV001679801]	benign	15	82859196	82859196	Human		name
150463755	CV1263852	single nucleotide variant	NM_004839.4(HOMER2):c.651+28G>C	not provided [RCV001682553]	benign	15	82854616	82854616	Human		name
150542939	CV1306660	single nucleotide variant	NM_004839.4(HOMER2):c.762+27C>G	not provided [RCV001769724]	likely benign	15	82852115	82852115	Human		name
150542443	CV1307769	single nucleotide variant	NM_004839.4(HOMER2):c.762+35G>A	not provided [RCV001769544]	likely benign	15	82852107	82852107	Human		name
150539398	CV1308758	single nucleotide variant	NM_004839.4(HOMER2):c.495-14T>A	not provided [RCV001766262]	benign\|likely benign	15	82854814	82854814	Human		name
150543491	CV1308998	deletion	NM_004839.4(HOMER2):c.387+41del	not provided [RCV001769911]	likely benign	15	82864126	82864126	Human		name
151750508	CV1335554	single nucleotide variant	NM_004839.4(HOMER2):c.844-43C>A	not provided [RCV001847396]	likely benign	15	82849946	82849946	Human		name
152054067	CV1553737	single nucleotide variant	NM_004839.4(HOMER2):c.495-13C>A	not provided [RCV002146025]	likely benign	15	82854813	82854813	Human		name
152113914	CV1573575	single nucleotide variant	NM_004839.4(HOMER2):c.495-20C>T	not provided [RCV002215871]	benign	15	82854820	82854820	Human		name
152166796	CV1597226	single nucleotide variant	NM_004839.4(HOMER2):c.495-19G>A	not provided [RCV002204519]	likely benign	15	82854819	82854819	Human		name
152064427	CV1612275	single nucleotide variant	NM_004839.4(HOMER2):c.295-15A>G	not provided [RCV002128770]	likely benign	15	82864274	82864274	Human		name
152173281	CV1637739	single nucleotide variant	NM_004839.4(HOMER2):c.651+19G>C	not provided [RCV002162751]	likely benign	15	82854625	82854625	Human		name
153349953	CV1693656	single nucleotide variant	NM_004839.4(HOMER2):c.388-17C>G	not provided [RCV002276389]	likely benign	15	82859152	82859152	Human		name
156222872	CV2005807	single nucleotide variant	NM_004839.4(HOMER2):c.388-16C>T	not provided [RCV002667293]	likely benign	15	82859151	82859151	Human		name
405236153	CV3038031	single nucleotide variant	NM_004839.4(HOMER2):c.163-12G>T	not provided [RCV003712392]	likely benign	15	82875416	82875416	Human		name
405176276	CV3119292	single nucleotide variant	NM_004839.4(HOMER2):c.762+17C>T	not provided [RCV003819577]\|not specified [RCV004801408]	likely benign	15	82852125	82852125	Human		name
405229840	CV3153576	single nucleotide variant	NM_004839.4(HOMER2):c.294+19C>T	not provided [RCV003848641]	likely benign	15	82875254	82875254	Human		name
405082340	CV3166812	single nucleotide variant	NM_004839.4(HOMER2):c.652-18G>A	not provided [RCV003851586]	likely benign	15	82852270	82852270	Human		name
404989673	CV3179995	single nucleotide variant	NM_004839.4(HOMER2):c.495-16C>T	not provided [RCV003881473]	likely benign	15	82854816	82854816	Human		name
596942185	CV3544010	single nucleotide variant	NM_004839.4(HOMER2):c.295-11T>C	not specified [RCV004800000]	likely benign	15	82864270	82864270	Human		name
596943626	CV3544311	single nucleotide variant	NM_004839.4(HOMER2):c.763-15A>T	not specified [RCV004800791]	likely benign	15	82851246	82851246	Human		name
597691858	CV3679506	single nucleotide variant	NM_004839.4(HOMER2):c.388-12T>C	Inborn genetic diseases [RCV004985894]	uncertain significance	15	82859147	82859147	Human	1	name
597936572	CV3759616	single nucleotide variant	NM_004839.4(HOMER2):c.495-15G>A	not provided [RCV005076736]	likely benign	15	82854815	82854815	Human		name
597860212	CV3826012	single nucleotide variant	NM_004839.4(HOMER2):c.651+14A>G	not provided [RCV005174910]	likely benign	15	82854630	82854630	Human		name
616933945	CV4011918	single nucleotide variant	NM_004839.4(HOMER2):c.762+18G>A	not specified [RCV005408467]	likely benign	15	82852124	82852124	Human		name
14745484	CV668045	single nucleotide variant	NM_004839.4(HOMER2):c.844-47C>T	not provided [RCV000843423]	benign	15	82849950	82849950	Human		name
150334227	CV1172778	single nucleotide variant	NM_004839.4(HOMER2):c.763-245T>C	not provided [RCV001539892]	benign	15	82851476	82851476	Human		name
150503743	CV1212544	duplication	NM_004839.4(HOMER2):c.388-179dup	not provided [RCV001595419]	benign	15	82859304	82859305	Human		name
150516207	CV1216478	single nucleotide variant	NM_004839.4(HOMER2):c.762+312C>T	not provided [RCV001608669]	benign	15	82851830	82851830	Human		name
150506852	CV1226447	single nucleotide variant	NM_004839.4(HOMER2):c.294+177G>T	not provided [RCV001635815]	benign	15	82875096	82875096	Human		name
150472520	CV1252258	single nucleotide variant	NM_004839.4(HOMER2):c.162+295A>G	not provided [RCV001671459]	benign	15	82892390	82892390	Human		name
150453928	CV1260584	single nucleotide variant	NM_004839.4(HOMER2):c.162+142C>T	not provided [RCV001681077]	benign	15	82892543	82892543	Human		name
150454454	CV1266009	single nucleotide variant	NM_004839.4(HOMER2):c.494+219A>T	not provided [RCV001692586]	benign	15	82858810	82858810	Human		name
150467299	CV1277547	single nucleotide variant	NM_004839.4(HOMER2):c.294+319T>C	not provided [RCV001710842]	benign	15	82874954	82874954	Human		name
150437983	CV1286634	single nucleotide variant	NM_004839.4(HOMER2):c.651+233T>C	not provided [RCV001724713]	benign	15	82854411	82854411	Human		name
150534651	CV1307897	single nucleotide variant	NM_004839.4(HOMER2):c.762+124G>A	not provided [RCV001757619]	likely benign	15	82852018	82852018	Human		name
155994294	CV2095658	deletion	NM_004839.4(HOMER2):c.6-9_6-8del	not provided [RCV002908308]	likely benign	15	82892849	82892850	Human		name
405166414	CV2957343	deletion	NM_004839.4(HOMER2):c.5+7_5+34del	not provided [RCV003675022]	uncertain significance	15	82952497	82952524	Human		name
151789729	CV1394284	deletion	NM_004839.4(HOMER2):c.388-8_388-3del	not provided [RCV002046985]	uncertain significance	15	82859138	82859143	Human		name
150532520	CV1306796	single nucleotide variant	NM_004839.4(HOMER2):c.93G>A (p.Ala31=)	not provided [RCV001757794]	likely benign	15	82892754	82892754	Human		name
156309090	CV1924963	single nucleotide variant	NM_004839.4(HOMER2):c.66G>A (p.Lys22=)	not provided [RCV002629653]	likely benign	15	82892781	82892781	Human		name
13515796	CV491477	single nucleotide variant	NM_004839.4(HOMER2):c.33G>A (p.Ala11=)	not provided [RCV000594734]	conflicting interpretations of pathogenicity\|uncertain significance	15	82892814	82892814	Human		name
152034145	CV1621484	single nucleotide variant	NM_004839.4(HOMER2):c.153C>T (p.Asp51=)	not provided [RCV002205297]	likely benign	15	82892694	82892694	Human		name
41406528	CV982927	single nucleotide variant	NM_004839.4(HOMER2):c.234C>T (p.Ala78=)	HOMER2-related disorder [RCV004753263]\|not provided [RCV001751549]\|not specified [RCV001288632]	benign\|likely benign	15	82875333	82875333	Human	1	name , trait , alternate_id
126912936	CV1038364	single nucleotide variant	NM_004839.4(HOMER2):c.89A>G (p.Gln30Arg)	not provided [RCV001356917]	likely benign\|uncertain significance	15	82892758	82892758	Human		name
150550302	CV1309184	single nucleotide variant	NM_004839.4(HOMER2):c.969C>T (p.Asp323=)	not provided [RCV001752865]	likely benign	15	82849778	82849778	Human		name
151727001	CV1408070	single nucleotide variant	NM_004839.4(HOMER2):c.80C>T (p.Ala27Val)	not provided [RCV001891851]	uncertain significance	15	82892767	82892767	Human		name
151847757	CV1461968	single nucleotide variant	NM_004839.4(HOMER2):c.29G>A (p.Arg10Gln)	not provided [RCV001936941]	likely benign\|uncertain significance	15	82892818	82892818	Human		name
152109317	CV1563857	single nucleotide variant	NM_004839.4(HOMER2):c.525G>A (p.Glu175=)	not provided [RCV002174129]	likely benign	15	82854770	82854770	Human		name
152069149	CV1570806	single nucleotide variant	NM_004839.4(HOMER2):c.402C>T (p.Asn134=)	not provided [RCV002129373]	likely benign	15	82859121	82859121	Human		name
156081056	CV1883578	single nucleotide variant	NM_004839.4(HOMER2):c.432C>T (p.Ala144=)	not provided [RCV003079868]	likely benign	15	82859091	82859091	Human		name
156201691	CV1925637	single nucleotide variant	NM_004839.4(HOMER2):c.594G>A (p.Glu198=)	not provided [RCV002643654]	benign	15	82854701	82854701	Human		name
156381376	CV1994767	single nucleotide variant	NM_004839.4(HOMER2):c.351G>A (p.Thr117=)	not provided [RCV002653684]	likely benign	15	82864203	82864203	Human		name
329381001	CV2440439	single nucleotide variant	NM_004839.4(HOMER2):c.77C>T (p.Pro26Leu)	Inborn genetic diseases [RCV003175509]\|not provided [RCV005101260]	uncertain significance	15	82892770	82892770	Human	1	name
405092582	CV2859410	single nucleotide variant	NM_004839.4(HOMER2):c.41T>A (p.Phe14Tyr)	not provided [RCV003549887]	uncertain significance	15	82892806	82892806	Human		name
405178190	CV2861206	single nucleotide variant	NM_004839.4(HOMER2):c.915A>G (p.Lys305=)	not provided [RCV003542949]	likely benign	15	82849832	82849832	Human		name
405178561	CV2913084	single nucleotide variant	NM_004839.4(HOMER2):c.711G>A (p.Gln237=)	not provided [RCV003563754]	likely benign	15	82852193	82852193	Human		name
405208890	CV3065541	single nucleotide variant	NM_004839.4(HOMER2):c.55A>G (p.Asn19Asp)	not provided [RCV003731705]	uncertain significance	15	82892792	82892792	Human		name
404993883	CV3132525	single nucleotide variant	NM_004839.4(HOMER2):c.591G>A (p.Val197=)	not provided [RCV003827464]	likely benign	15	82854704	82854704	Human		name
405284069	CV3213564	single nucleotide variant	NM_004839.4(HOMER2):c.732G>A (p.Glu244=)	HOMER2-related disorder [RCV003922138]	likely benign	15	82852172	82852172	Human		name , trait , alternate_id
405271601	CV3219086	single nucleotide variant	NM_004839.4(HOMER2):c.489G>A (p.Thr163=)	HOMER2-related disorder [RCV003971794]	likely benign	15	82859034	82859034	Human		name , trait , alternate_id
405695880	CV3226688	single nucleotide variant	NM_004839.4(HOMER2):c.504C>T (p.Asn168=)	not provided [RCV003993081]	likely benign	15	82854791	82854791	Human		name
596946569	CV3548393	single nucleotide variant	NM_004839.4(HOMER2):c.795C>T (p.Ile265=)	not provided [RCV004810219]	likely benign	15	82851199	82851199	Human		name
597855563	CV3738179	single nucleotide variant	NM_004839.4(HOMER2):c.846G>A (p.Ala282=)	not provided [RCV005066762]	uncertain significance	15	82849901	82849901	Human		name
597957921	CV3754819	single nucleotide variant	NM_004839.4(HOMER2):c.522C>T (p.Ile174=)	not provided [RCV005080669]	likely benign	15	82854773	82854773	Human		name
13516620	CV492438	single nucleotide variant	NM_004839.4(HOMER2):c.363C>T (p.Ile121=)	HOMER2-related disorder [RCV003952988]\|not provided [RCV001696964]\|not specified [RCV000595756]	benign\|likely benign	15	82864191	82864191	Human	1	name , trait , alternate_id
13530359	CV505224	single nucleotide variant	NM_004839.4(HOMER2):c.393C>T (p.Ser131=)	not specified [RCV000600670]	likely benign	15	82859130	82859130	Human		name
13528915	CV505420	single nucleotide variant	NM_004839.4(HOMER2):c.819C>T (p.Cys273=)	HOMER2-related disorder [RCV003917909]\|not provided [RCV000992158]\|not specified [RCV000600162]	benign	15	82851175	82851175	Human	1	name , trait , alternate_id
13537105	CV505844	single nucleotide variant	NM_004839.4(HOMER2):c.981C>T (p.Asp327=)	not provided [RCV000992154]\|not specified [RCV000609934]	benign	15	82849766	82849766	Human		name
126743334	CV1021371	single nucleotide variant	NM_004839.4(HOMER2):c.130A>G (p.Ser44Gly)	Autosomal dominant nonsyndromic hearing loss 68 [RCV001336747]	uncertain significance	15	82892717	82892717	Human	1	name
156435199	CV1940638	single nucleotide variant	NM_004839.4(HOMER2):c.100G>A (p.Val34Ile)	not provided [RCV003104747]	uncertain significance	15	82892747	82892747	Human		name
156415404	CV1958392	single nucleotide variant	NM_004839.4(HOMER2):c.214C>A (p.Gln72Lys)	Inborn genetic diseases [RCV004064515]\|not provided [RCV002589149]	likely benign\|uncertain significance	15	82875353	82875353	Human	1	name
156188827	CV1997949	single nucleotide variant	NM_004839.4(HOMER2):c.1023C>T (p.Thr341=)	not provided [RCV002643251]	likely benign	15	82849724	82849724	Human		name
156243447	CV2148871	single nucleotide variant	NM_004839.4(HOMER2):c.188C>A (p.Pro63Gln)	not provided [RCV003008184]	uncertain significance	15	82875379	82875379	Human		name
404987503	CV2852560	single nucleotide variant	NM_004839.4(HOMER2):c.107A>G (p.Tyr36Cys)	not specified [RCV003489772]	uncertain significance	15	82892740	82892740	Human		name
597691903	CV3679511	single nucleotide variant	NM_004839.4(HOMER2):c.245C>T (p.Ala82Val)	Inborn genetic diseases [RCV004985899]	uncertain significance	15	82875322	82875322	Human	1	name
597691906	CV3679512	single nucleotide variant	NM_004839.4(HOMER2):c.169A>C (p.Ile57Leu)	Inborn genetic diseases [RCV004985900]	uncertain significance	15	82875398	82875398	Human	1	name
597691915	CV3679513	single nucleotide variant	NM_004839.4(HOMER2):c.200T>A (p.Phe67Tyr)	Inborn genetic diseases [RCV004985901]	uncertain significance	15	82875367	82875367	Human	1	name
597914252	CV3740613	single nucleotide variant	NM_004839.4(HOMER2):c.1020C>T (p.Gly340=)	not provided [RCV005073950]	uncertain significance	15	82849727	82849727	Human		name
597914564	CV3740648	single nucleotide variant	NM_004839.4(HOMER2):c.136C>T (p.Arg46Trp)	not provided [RCV005073985]	uncertain significance	15	82892711	82892711	Human		name
597846418	CV3753040	single nucleotide variant	NM_004839.4(HOMER2):c.154G>A (p.Gly52Arg)	not provided [RCV005087265]	uncertain significance	15	82892693	82892693	Human		name
597926113	CV3840648	single nucleotide variant	NM_004839.4(HOMER2):c.134A>G (p.Tyr45Cys)	not provided [RCV005185119]	uncertain significance	15	82892713	82892713	Human		name
598191137	CV3975542	single nucleotide variant	NM_004839.4(HOMER2):c.170T>C (p.Ile57Thr)	Inborn genetic diseases [RCV005354238]	uncertain significance	15	82875397	82875397	Human	1	name
598191147	CV3975546	single nucleotide variant	NM_004839.4(HOMER2):c.137G>A (p.Arg46Gln)	Inborn genetic diseases [RCV005354240]	uncertain significance	15	82892710	82892710	Human	1	name
13529275	CV505843	single nucleotide variant	NM_004839.4(HOMER2):c.1023C>G (p.Thr341=)	HOMER2-related disorder [RCV003962794]\|not provided [RCV001698087]	benign\|likely benign	15	82849724	82849724	Human	1	name , trait , alternate_id
14705796	CV656312	single nucleotide variant	NM_004839.4(HOMER2):c.181A>G (p.Ile61Val)	HOMER2-related disorder [RCV003928296]\|Inborn genetic diseases [RCV002536081]\|not provided [RCV000826310]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	15	82875386	82875386	Human	2	name , trait , alternate_id
34890294	CV916783	duplication	NM_004839.4(HOMER2):c.807dup (p.Met270fs)	Autosomal dominant nonsyndromic hearing loss 68 [RCV001181995]	pathogenic	15	82851186	82851187	Human	1	name
126913727	CV1038363	single nucleotide variant	NM_004839.4(HOMER2):c.430G>A (p.Ala144Thr)	not provided [RCV001357640]	uncertain significance	15	82859093	82859093	Human		name
150493357	CV1267130	single nucleotide variant	NM_004839.4(HOMER2):c.539G>A (p.Arg180Gln)	Inborn genetic diseases [RCV002538613]\|not provided [RCV001688157]	benign\|likely benign\|uncertain significance	15	82854756	82854756	Human	1	name
150532367	CV1307873	single nucleotide variant	NM_004839.4(HOMER2):c.707C>T (p.Thr236Met)	not provided [RCV001757595]	likely benign	15	82852197	82852197	Human		name
150550313	CV1309207	single nucleotide variant	NM_004839.4(HOMER2):c.638G>A (p.Arg213Gln)	Autosomal dominant nonsyndromic hearing loss 68 [RCV005397010]\|not provided [RCV001752888]	benign\|likely benign	15	82854657	82854657	Human	1	name
150550358	CV1309289	single nucleotide variant	NM_004839.4(HOMER2):c.793A>G (p.Ile265Val)	not provided [RCV001752970]	benign\|likely benign	15	82851201	82851201	Human		name
151842358	CV1357663	single nucleotide variant	NM_004839.4(HOMER2):c.702G>C (p.Lys234Asn)	Inborn genetic diseases [RCV004041395]\|not provided [RCV001881509]	uncertain significance	15	82852202	82852202	Human	1	name
151760361	CV1403985	single nucleotide variant	NM_004839.4(HOMER2):c.977T>C (p.Ile326Thr)	not provided [RCV002007788]	uncertain significance	15	82849770	82849770	Human		name
151751130	CV1426697	single nucleotide variant	NM_004839.4(HOMER2):c.799C>A (p.Pro267Thr)	not provided [RCV002006875]	uncertain significance	15	82851195	82851195	Human		name
151748428	CV1442294	single nucleotide variant	NM_004839.4(HOMER2):c.650A>G (p.Lys217Arg)	not provided [RCV002043010]	uncertain significance	15	82854645	82854645	Human		name
151780004	CV1473941	single nucleotide variant	NM_004839.4(HOMER2):c.925C>T (p.Arg309Cys)	not provided [RCV001864874]	uncertain significance	15	82849822	82849822	Human		name
151814322	CV1494823	single nucleotide variant	NM_004839.4(HOMER2):c.815A>G (p.Glu272Gly)	not provided [RCV001954131]	uncertain significance	15	82851179	82851179	Human		name
151759922	CV1503964	single nucleotide variant	NM_004839.4(HOMER2):c.554G>A (p.Arg185Gln)	not provided [RCV002007737]	uncertain significance	15	82854741	82854741	Human		name
152101627	CV1621860	single nucleotide variant	NM_004839.4(HOMER2):c.358A>G (p.Lys120Glu)	HOMER2-related disorder [RCV003951068]\|Inborn genetic diseases [RCV003015329]\|not provided [RCV002115419]	benign\|likely benign\|uncertain significance	15	82864196	82864196	Human	2	name , trait , alternate_id
155726631	CV1773685	single nucleotide variant	NM_004839.4(HOMER2):c.672A>T (p.Gln224His)	not provided [RCV002301473]	uncertain significance	15	82852232	82852232	Human		name
156323036	CV1870850	single nucleotide variant	NM_004839.4(HOMER2):c.727G>A (p.Glu243Lys)	not provided [RCV003063204]	likely benign\|uncertain significance	15	82852177	82852177	Human		name
156376991	CV1896212	single nucleotide variant	NM_004839.4(HOMER2):c.613T>G (p.Ser205Ala)	not provided [RCV003092956]	uncertain significance	15	82854682	82854682	Human		name
156351917	CV1923416	single nucleotide variant	NM_004839.4(HOMER2):c.998G>A (p.Arg333His)	not provided [RCV002650957]	uncertain significance	15	82849749	82849749	Human		name
156445152	CV1945151	single nucleotide variant	NM_004839.4(HOMER2):c.779G>A (p.Arg260Gln)	not provided [RCV003116089]	uncertain significance	15	82851215	82851215	Human		name
156079190	CV1975683	single nucleotide variant	NM_004839.4(HOMER2):c.335T>C (p.Ile112Thr)	not provided [RCV002621486]	likely benign	15	82864219	82864219	Human		name
155996891	CV2109527	single nucleotide variant	NM_004839.4(HOMER2):c.751G>C (p.Glu251Gln)	not provided [RCV002947601]	uncertain significance	15	82852153	82852153	Human		name
156077879	CV2141875	single nucleotide variant	NM_004839.4(HOMER2):c.494G>A (p.Ser165Asn)	not provided [RCV002979156]	uncertain significance	15	82859029	82859029	Human		name
10450108	CV215059	single nucleotide variant	NM_004839.4(HOMER2):c.554G>C (p.Arg185Pro)	Autosomal dominant nonsyndromic hearing loss 68 [RCV000202595]	pathogenic	15	82854741	82854741	Human	1	name
156000857	CV2284410	single nucleotide variant	NM_004839.4(HOMER2):c.797T>C (p.Ile266Thr)	Inborn genetic diseases [RCV002865341]	uncertain significance	15	82851197	82851197	Human	1	name
156006556	CV2288850	single nucleotide variant	NM_004839.4(HOMER2):c.407C>T (p.Thr136Met)	Inborn genetic diseases [RCV002865824]\|not provided [RCV003730295]	uncertain significance	15	82859116	82859116	Human	1	name
156162277	CV2323521	single nucleotide variant	NM_004839.4(HOMER2):c.541G>C (p.Glu181Gln)	Inborn genetic diseases [RCV002929346]	uncertain significance	15	82854754	82854754	Human	1	name
156351565	CV2323783	single nucleotide variant	NM_004839.4(HOMER2):c.505G>A (p.Val169Met)	Inborn genetic diseases [RCV002939954]\|not provided [RCV003777960]	uncertain significance	15	82854790	82854790	Human	1	name
155998936	CV2396334	single nucleotide variant	NM_004839.4(HOMER2):c.578C>T (p.Ser193Leu)	Inborn genetic diseases [RCV002779215]	uncertain significance	15	82854717	82854717	Human	1	name
401728972	CV2673108	single nucleotide variant	NM_004839.4(HOMER2):c.765G>C (p.Glu255Asp)	Inborn genetic diseases [RCV003247650]	uncertain significance	15	82851229	82851229	Human	1	name
401728459	CV2686107	single nucleotide variant	NM_004839.4(HOMER2):c.488C>T (p.Thr163Met)	Inborn genetic diseases [RCV003270612]\|not provided [RCV005102550]	uncertain significance	15	82859035	82859035	Human	1	name
401866125	CV2775427	single nucleotide variant	NM_004839.4(HOMER2):c.587G>C (p.Ser196Thr)	Inborn genetic diseases [RCV003359896]\|not provided [RCV005061328]	uncertain significance	15	82854708	82854708	Human	1	name
401931328	CV2800862	single nucleotide variant	NM_004839.4(HOMER2):c.944T>A (p.Leu315Ter)	HOMER2-related disorder [RCV003391315]	uncertain significance	15	82849803	82849803	Human		name , trait , alternate_id
401936341	CV2802920	single nucleotide variant	NM_004839.4(HOMER2):c.637C>T (p.Arg213Trp)	HOMER2-related disorder [RCV003414209]	uncertain significance	15	82854658	82854658	Human		name , trait , alternate_id
402476391	CV2857272	single nucleotide variant	NM_004839.4(HOMER2):c.499G>A (p.Ala167Thr)	not provided [RCV003543445]	likely benign	15	82854796	82854796	Human		name
405161921	CV2951407	single nucleotide variant	NM_004839.4(HOMER2):c.373A>G (p.Ser125Gly)	not provided [RCV003670790]	uncertain significance	15	82864181	82864181	Human		name
402483752	CV2998157	single nucleotide variant	NM_004839.4(HOMER2):c.974A>G (p.Lys325Arg)	not provided [RCV003686864]	likely benign	15	82849773	82849773	Human		name
405090999	CV3044828	single nucleotide variant	NM_004839.4(HOMER2):c.967G>A (p.Asp323Asn)	not provided [RCV003717817]	likely benign\|uncertain significance	15	82849780	82849780	Human		name
405118880	CV3116042	single nucleotide variant	NM_004839.4(HOMER2):c.896C>T (p.Thr299Ile)	not provided [RCV003814532]	uncertain significance	15	82849851	82849851	Human		name
405234856	CV3155603	single nucleotide variant	NM_004839.4(HOMER2):c.497C>T (p.Ala166Val)	not provided [RCV003853581]	likely benign	15	82854798	82854798	Human		name
405791450	CV3267037	single nucleotide variant	NM_004839.4(HOMER2):c.650A>C (p.Lys217Thr)	Inborn genetic diseases [RCV004399860]\|not provided [RCV005104468]	uncertain significance	15	82854645	82854645	Human	1	name
408384840	CV3506341	single nucleotide variant	NM_004839.4(HOMER2):c.628G>A (p.Glu210Lys)	HOMER2-related disorder [RCV004732159]	uncertain significance	15	82854667	82854667	Human		name , trait , alternate_id
408380022	CV3509613	single nucleotide variant	NM_004839.4(HOMER2):c.506T>C (p.Val169Ala)	HOMER2-related disorder [RCV004753889]	uncertain significance	15	82854789	82854789	Human		name , trait , alternate_id
596920767	CV3534244	single nucleotide variant	NM_004839.4(HOMER2):c.543G>C (p.Glu181Asp)	not specified [RCV004783463]	likely benign	15	82854752	82854752	Human		name
597693151	CV3679505	single nucleotide variant	NM_004839.4(HOMER2):c.644G>A (p.Arg215His)	Inborn genetic diseases [RCV004985893]	uncertain significance	15	82854651	82854651	Human	1	name
597691881	CV3679508	single nucleotide variant	NM_004839.4(HOMER2):c.775C>T (p.Leu259Phe)	Inborn genetic diseases [RCV004985896]	uncertain significance	15	82851219	82851219	Human	1	name
597691888	CV3679509	single nucleotide variant	NM_004839.4(HOMER2):c.920G>A (p.Arg307Gln)	Inborn genetic diseases [RCV004985897]	uncertain significance	15	82849827	82849827	Human	1	name
597691895	CV3679510	single nucleotide variant	NM_004839.4(HOMER2):c.820G>A (p.Glu274Lys)	Inborn genetic diseases [RCV004985898]	uncertain significance	15	82851174	82851174	Human	1	name
597914101	CV3740592	single nucleotide variant	NM_004839.4(HOMER2):c.394A>T (p.Ser132Cys)	not provided [RCV005073929]	uncertain significance	15	82859129	82859129	Human		name
597936869	CV3759858	single nucleotide variant	NM_004839.4(HOMER2):c.601A>G (p.Lys201Glu)	not provided [RCV005076780]	uncertain significance	15	82854694	82854694	Human		name
597920081	CV3781204	single nucleotide variant	NM_004839.4(HOMER2):c.958G>A (p.Glu320Lys)	not provided [RCV005130086]	uncertain significance	15	82849789	82849789	Human		name
597958000	CV3796867	single nucleotide variant	NM_004839.4(HOMER2):c.696G>C (p.Lys232Asn)	not provided [RCV005137765]	uncertain significance	15	82852208	82852208	Human		name
597859009	CV3817099	single nucleotide variant	NM_004839.4(HOMER2):c.702G>T (p.Lys234Asn)	not provided [RCV005146480]	uncertain significance	15	82852202	82852202	Human		name
597897932	CV3826562	single nucleotide variant	NM_004839.4(HOMER2):c.856G>A (p.Asp286Asn)	not provided [RCV005180695]	uncertain significance	15	82849891	82849891	Human		name
598191131	CV3975541	single nucleotide variant	NM_004839.4(HOMER2):c.622C>T (p.Arg208Cys)	Inborn genetic diseases [RCV005354237]	uncertain significance	15	82854673	82854673	Human	1	name
598191140	CV3975543	single nucleotide variant	NM_004839.4(HOMER2):c.749G>A (p.Arg250Gln)	Inborn genetic diseases [RCV005354239]	uncertain significance	15	82852155	82852155	Human	1	name
598248988	CV3975544	single nucleotide variant	NM_004839.4(HOMER2):c.428A>T (p.His143Leu)	Inborn genetic diseases [RCV005345523]	uncertain significance	15	82859095	82859095	Human	1	name
598248993	CV3975545	single nucleotide variant	NM_004839.4(HOMER2):c.403G>A (p.Gly135Arg)	Inborn genetic diseases [RCV005345524]	uncertain significance	15	82859120	82859120	Human	1	name
598198869	CV4007235	single nucleotide variant	NM_004839.4(HOMER2):c.854G>A (p.Arg285Lys)	Autosomal dominant nonsyndromic hearing loss 68 [RCV005398063]	uncertain significance	15	82849893	82849893	Human	1	name
13517605	CV491722	single nucleotide variant	NM_004839.4(HOMER2):c.643C>T (p.Arg215Cys)	not provided [RCV000596644]	conflicting interpretations of pathogenicity\|uncertain significance	15	82854652	82854652	Human		name
13516853	CV492268	single nucleotide variant	NM_004839.4(HOMER2):c.609G>T (p.Gln203His)	HOMER2-related disorder [RCV003915729]\|Inborn genetic diseases [RCV004629250]\|not provided [RCV000596040]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	15	82854686	82854686	Human	2	name , trait , alternate_id
13541793	CV504993	single nucleotide variant	NM_004839.4(HOMER2):c.764A>G (p.Glu255Gly)	not provided [RCV000971947]\|not specified [RCV000616651]	benign\|likely benign	15	82851230	82851230	Human		name
13531710	CV505222	single nucleotide variant	NM_004839.4(HOMER2):c.623G>A (p.Arg208His)	not provided [RCV000957332]\|not specified [RCV000606562]	benign	15	82854672	82854672	Human		name
21066578	CV793555	single nucleotide variant	NM_004839.4(HOMER2):c.350C>T (p.Thr117Met)	not provided [RCV000992155]	uncertain significance	15	82864204	82864204	Human		name
151764183	CV1403112	single nucleotide variant	NM_004839.4(HOMER2):c.1004G>A (p.Gly335Glu)	Inborn genetic diseases [RCV002557859]\|not provided [RCV001914330]	uncertain significance	15	82849743	82849743	Human	1	name
152141789	CV1588575	indel	NM_004839.4(HOMER2):c.495-15_495-14delinsTC	not provided [RCV002200668]	likely benign	15	82854814	82854815	Human		name
156202979	CV2076567	single nucleotide variant	NM_004839.4(HOMER2):c.1031A>T (p.Ter344Leu)	not provided [RCV002852533]	uncertain significance	15	82849716	82849716	Human		name
405124619	CV2889576	single nucleotide variant	NM_004839.4(HOMER2):c.1025A>G (p.Asp342Gly)	HOMER2-related disorder [RCV003966516]\|not provided [RCV003559446]	benign\|likely benign	15	82849722	82849722	Human	1	name , trait , alternate_id
402499107	CV2922810	single nucleotide variant	NM_004839.4(HOMER2):c.1030T>G (p.Ter344Glu)	not provided [RCV003573806]	uncertain significance	15	82849717	82849717	Human		name
405855140	CV3395738	single nucleotide variant	NM_004839.4(HOMER2):c.1022C>A (p.Thr341Asn)	Autosomal dominant nonsyndromic hearing loss 68 [RCV004556001]	uncertain significance	15	82849725	82849725	Human	1	name
408380314	CV3514408	single nucleotide variant	NM_004839.4(HOMER2):c.1016T>A (p.Leu339Gln)	HOMER2-related disorder [RCV004754117]	uncertain significance	15	82849731	82849731	Human		name , trait , alternate_id
597691869	CV3679507	single nucleotide variant	NM_004839.4(HOMER2):c.1001G>A (p.Arg334Gln)	Inborn genetic diseases [RCV004985895]\|not provided [RCV005110354]	uncertain significance	15	82849746	82849746	Human	1	name
597660617	CV3731848	single nucleotide variant	NM_004839.4(HOMER2):c.1031A>G (p.Ter344Trp)	Autosomal dominant nonsyndromic hearing loss 68 [RCV005002070]	likely pathogenic	15	82849716	82849716	Human	1	name
126730615	CV1001324	deletion	NM_004839.4(HOMER2):c.799_803del (p.Pro267fs)	Autosomal dominant nonsyndromic hearing loss 68 [RCV001327994]	pathogenic	15	82851191	82851195	Human	1	name
150542405	CV1307760	insertion	NM_004839.4(HOMER2):c.388-180_388-179insGTTTA	not provided [RCV001769535]	likely benign	15	82859314	82859315	Human		name
597721666	CV3733786	deletion	NM_004839.4(HOMER2):c.1023_1029del (p.Asp342fs)	Autosomal dominant nonsyndromic hearing loss 68 [RCV005053091]	likely pathogenic	15	82849718	82849724	Human	1	name

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