Wipf3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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68 records found for search term Wipf3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405811946	CV3352773	single nucleotide variant	NM_001080529.3(WIPF3):c.5C>T (p.Pro2Leu)	not specified [RCV004482971]	uncertain significance	7	29834729	29834729	Human		name
407524615	CV3487886	single nucleotide variant	NM_001080529.3(WIPF3):c.23C>T (p.Pro8Leu)	not specified [RCV004678489]	uncertain significance	7	29834747	29834747	Human		name
156012906	CV2300375	single nucleotide variant	NM_001080529.3(WIPF3):c.202C>T (p.Arg68Cys)	not specified [RCV004153585]	uncertain significance	7	29875941	29875941	Human		name
156099905	CV2367448	single nucleotide variant	NM_001080529.3(WIPF3):c.167G>A (p.Gly56Glu)	not specified [RCV004211391]	uncertain significance	7	29875906	29875906	Human		name
401737178	CV2718010	single nucleotide variant	NM_001080529.3(WIPF3):c.243A>T (p.Lys81Asn)	not specified [RCV004321951]	uncertain significance	7	29879028	29879028	Human		name
405811835	CV3352770	single nucleotide variant	NM_001080529.3(WIPF3):c.137G>A (p.Arg46Gln)	not specified [RCV004482968]	uncertain significance	7	29875876	29875876	Human		name
407524624	CV3487889	single nucleotide variant	NM_001080529.3(WIPF3):c.259G>A (p.Ala87Thr)	not specified [RCV004678492]	uncertain significance	7	29879044	29879044	Human		name
407524628	CV3487890	single nucleotide variant	NM_001080529.3(WIPF3):c.158T>C (p.Ile53Thr)	not specified [RCV004678493]	uncertain significance	7	29875897	29875897	Human		name
598267248	CV3929734	single nucleotide variant	NM_001080529.3(WIPF3):c.269G>A (p.Arg90Gln)	not specified [RCV005302136]	uncertain significance	7	29879054	29879054	Human		name
598267256	CV3929736	single nucleotide variant	NM_001080529.3(WIPF3):c.263A>G (p.Asn88Ser)	not specified [RCV005302138]	uncertain significance	7	29879048	29879048	Human		name
15120439	CV750612	single nucleotide variant	NM_001080529.3(WIPF3):c.1383A>G (p.Glu461=)	not provided [RCV000918322]	benign	7	29904317	29904317	Human		name
156039442	CV2215205	single nucleotide variant	NM_001080529.3(WIPF3):c.410A>G (p.Asn137Ser)	not specified [RCV004086917]	uncertain significance	7	29883904	29883904	Human		name
156233090	CV2273873	single nucleotide variant	NM_001080529.3(WIPF3):c.635T>C (p.Leu212Pro)	not specified [RCV004132497]	likely benign	7	29884129	29884129	Human		name
156190487	CV2289270	single nucleotide variant	NM_001080529.3(WIPF3):c.755T>G (p.Leu252Arg)	not specified [RCV004152255]	uncertain significance	7	29884249	29884249	Human		name
156070439	CV2295813	single nucleotide variant	NM_001080529.3(WIPF3):c.886C>T (p.Leu296Phe)	not specified [RCV004151734]	uncertain significance	7	29884380	29884380	Human		name
156171849	CV2326741	single nucleotide variant	NM_001080529.3(WIPF3):c.532A>T (p.Thr178Ser)	not specified [RCV004176586]	uncertain significance	7	29884026	29884026	Human		name
156236067	CV2346410	single nucleotide variant	NM_001080529.3(WIPF3):c.721T>C (p.Ser241Pro)	not specified [RCV004203888]	uncertain significance	7	29884215	29884215	Human		name
156016359	CV2360437	single nucleotide variant	NM_001080529.3(WIPF3):c.350T>C (p.Val117Ala)	not specified [RCV004208760]	likely benign	7	29879135	29879135	Human		name
156197947	CV2362746	single nucleotide variant	NM_001080529.3(WIPF3):c.647C>T (p.Ala216Val)	not specified [RCV004208864]	uncertain significance	7	29884141	29884141	Human		name
155927947	CV2366009	single nucleotide variant	NM_001080529.3(WIPF3):c.423C>G (p.Ser141Arg)	not specified [RCV004207610]	uncertain significance	7	29883917	29883917	Human		name
329368827	CV2450430	single nucleotide variant	NM_001080529.3(WIPF3):c.766C>T (p.His256Tyr)	not specified [RCV004265356]	uncertain significance	7	29884260	29884260	Human		name
329367486	CV2456803	single nucleotide variant	NM_001080529.3(WIPF3):c.385C>G (p.Arg129Gly)	not specified [RCV004270774]	uncertain significance	7	29883879	29883879	Human		name
401742543	CV2677616	single nucleotide variant	NM_001080529.3(WIPF3):c.551C>T (p.Pro184Leu)	not specified [RCV004291712]	uncertain significance	7	29884045	29884045	Human		name
401739787	CV2683168	single nucleotide variant	NM_001080529.3(WIPF3):c.649C>T (p.Pro217Ser)	not specified [RCV004286165]	uncertain significance	7	29884143	29884143	Human		name
401758820	CV2705161	single nucleotide variant	NM_001080529.3(WIPF3):c.632A>C (p.Asn211Thr)	not specified [RCV004310054]	uncertain significance	7	29884126	29884126	Human		name
401730425	CV2711300	single nucleotide variant	NM_001080529.3(WIPF3):c.607C>T (p.Pro203Ser)	not specified [RCV004313076]	uncertain significance	7	29884101	29884101	Human		name
401866801	CV2772837	single nucleotide variant	NM_001080529.3(WIPF3):c.743T>C (p.Val248Ala)	not specified [RCV004357622]	uncertain significance	7	29884237	29884237	Human		name
405811948	CV3352772	single nucleotide variant	NM_001080529.3(WIPF3):c.586A>G (p.Ile196Val)	not specified [RCV004482970]	uncertain significance	7	29884080	29884080	Human		name
405811944	CV3352774	single nucleotide variant	NM_001080529.3(WIPF3):c.646G>A (p.Ala216Thr)	not specified [RCV004482972]	uncertain significance	7	29884140	29884140	Human		name
405811942	CV3352775	single nucleotide variant	NM_001080529.3(WIPF3):c.649C>A (p.Pro217Thr)	not specified [RCV004482973]	uncertain significance	7	29884143	29884143	Human		name
405811940	CV3352776	single nucleotide variant	NM_001080529.3(WIPF3):c.653C>G (p.Pro218Arg)	not specified [RCV004482974]	uncertain significance	7	29884147	29884147	Human		name
405811938	CV3352777	single nucleotide variant	NM_001080529.3(WIPF3):c.697A>G (p.Thr233Ala)	not specified [RCV004482975]	uncertain significance	7	29884191	29884191	Human		name
405811937	CV3352778	single nucleotide variant	NM_001080529.3(WIPF3):c.698C>T (p.Thr233Met)	not specified [RCV004482976]	uncertain significance	7	29884192	29884192	Human		name
405811935	CV3352779	single nucleotide variant	NM_001080529.3(WIPF3):c.716C>T (p.Pro239Leu)	not specified [RCV004482977]	uncertain significance	7	29884210	29884210	Human		name
405811933	CV3352780	single nucleotide variant	NM_001080529.3(WIPF3):c.811G>A (p.Gly271Arg)	not specified [RCV004482978]	uncertain significance	7	29884305	29884305	Human		name
405811931	CV3352781	single nucleotide variant	NM_001080529.3(WIPF3):c.911C>T (p.Pro304Leu)	not specified [RCV004482979]	uncertain significance	7	29884405	29884405	Human		name
405811929	CV3352782	single nucleotide variant	NM_001080529.3(WIPF3):c.980C>T (p.Pro327Leu)	not specified [RCV004482980]	uncertain significance	7	29884474	29884474	Human		name
407524592	CV3487878	single nucleotide variant	NM_001080529.3(WIPF3):c.536C>T (p.Pro179Leu)	not specified [RCV004678481]	uncertain significance	7	29884030	29884030	Human		name
407524601	CV3487881	single nucleotide variant	NM_001080529.3(WIPF3):c.650C>A (p.Pro217His)	not specified [RCV004678484]	uncertain significance	7	29884144	29884144	Human		name
407524607	CV3487883	single nucleotide variant	NM_001080529.3(WIPF3):c.632A>G (p.Asn211Ser)	not specified [RCV004678486]	uncertain significance	7	29884126	29884126	Human		name
407524619	CV3487887	single nucleotide variant	NM_001080529.3(WIPF3):c.332C>G (p.Pro111Arg)	not specified [RCV004678490]	uncertain significance	7	29879117	29879117	Human		name
407524622	CV3487888	single nucleotide variant	NM_001080529.3(WIPF3):c.689C>T (p.Pro230Leu)	not specified [RCV004678491]	uncertain significance	7	29884183	29884183	Human		name
597792372	CV3630284	single nucleotide variant	NM_001080529.3(WIPF3):c.506C>T (p.Pro169Leu)	not specified [RCV004876972]	uncertain significance	7	29884000	29884000	Human		name
597792375	CV3630286	single nucleotide variant	NM_001080529.3(WIPF3):c.853G>C (p.Asp285His)	not specified [RCV004876973]	uncertain significance	7	29884347	29884347	Human		name
597739875	CV3630288	single nucleotide variant	NM_001080529.3(WIPF3):c.989C>G (p.Ser330Cys)	not specified [RCV004890419]	uncertain significance	7	29884483	29884483	Human		name
597792380	CV3630290	single nucleotide variant	NM_001080529.3(WIPF3):c.928G>C (p.Ala310Pro)	not specified [RCV004876974]	uncertain significance	7	29884422	29884422	Human		name
598267245	CV3929732	single nucleotide variant	NM_001080529.3(WIPF3):c.337G>T (p.Gly113Cys)	not specified [RCV005302135]	uncertain significance	7	29879122	29879122	Human		name
598267258	CV3929737	single nucleotide variant	NM_001080529.3(WIPF3):c.509A>G (p.Asn170Ser)	not specified [RCV005302139]	likely benign	7	29884003	29884003	Human		name
598267262	CV3929739	single nucleotide variant	NM_001080529.3(WIPF3):c.473C>A (p.Ala158Glu)	not specified [RCV005302140]	uncertain significance	7	29883967	29883967	Human		name
156279629	CV2297723	single nucleotide variant	NM_001080529.3(WIPF3):c.1049C>T (p.Ala350Val)	not specified [RCV004155401]	uncertain significance	7	29884543	29884543	Human		name
156179634	CV2356027	single nucleotide variant	NM_001080529.3(WIPF3):c.1156A>G (p.Thr386Ala)	not specified [RCV004201401]	uncertain significance	7	29888124	29888124	Human		name
401738944	CV2676407	single nucleotide variant	NM_001080529.3(WIPF3):c.1162C>A (p.Leu388Ile)	not specified [RCV004286428]	uncertain significance	7	29888130	29888130	Human		name
401752387	CV2682802	single nucleotide variant	NM_001080529.3(WIPF3):c.1199C>G (p.Pro400Arg)	not specified [RCV004281774]	uncertain significance	7	29888167	29888167	Human		name
401752409	CV2706999	single nucleotide variant	NM_001080529.3(WIPF3):c.1216G>A (p.Gly406Ser)	not specified [RCV004321596]	uncertain significance	7	29888184	29888184	Human		name
405811827	CV3352766	single nucleotide variant	NM_001080529.3(WIPF3):c.1024G>A (p.Ala342Thr)	not specified [RCV004482964]	uncertain significance	7	29884518	29884518	Human		name
405811829	CV3352767	single nucleotide variant	NM_001080529.3(WIPF3):c.1030G>A (p.Ala344Thr)	not specified [RCV004482965]	uncertain significance	7	29884524	29884524	Human		name
405811831	CV3352768	single nucleotide variant	NM_001080529.3(WIPF3):c.1093C>G (p.Arg365Gly)	not specified [RCV004482966]	uncertain significance	7	29884587	29884587	Human		name
405811833	CV3352769	single nucleotide variant	NM_001080529.3(WIPF3):c.1288G>A (p.Asp430Asn)	not specified [RCV004482967]	uncertain significance	7	29889344	29889344	Human		name
405811837	CV3352771	single nucleotide variant	NM_001080529.3(WIPF3):c.1420A>G (p.Asn474Asp)	not specified [RCV004482969]	uncertain significance	7	29904354	29904354	Human		name
407524595	CV3487879	single nucleotide variant	NM_001080529.3(WIPF3):c.1400C>T (p.Ser467Phe)	not specified [RCV004678482]	uncertain significance	7	29904334	29904334	Human		name
407524597	CV3487880	single nucleotide variant	NM_001080529.3(WIPF3):c.1162C>T (p.Leu388Phe)	not specified [RCV004678483]	uncertain significance	7	29888130	29888130	Human		name
407524604	CV3487882	single nucleotide variant	NM_001080529.3(WIPF3):c.1291T>G (p.Phe431Val)	not specified [RCV004678485]	uncertain significance	7	29889347	29889347	Human		name
407524631	CV3487891	single nucleotide variant	NM_001080529.3(WIPF3):c.1221A>T (p.Gln407His)	not specified [RCV004678494]	uncertain significance	7	29888189	29888189	Human		name
597739871	CV3630285	single nucleotide variant	NM_001080529.3(WIPF3):c.1309T>C (p.Tyr437His)	not specified [RCV004890418]	uncertain significance	7	29889365	29889365	Human		name
597739879	CV3630289	single nucleotide variant	NM_001080529.3(WIPF3):c.1034T>C (p.Leu345Ser)	not specified [RCV004890420]	uncertain significance	7	29884528	29884528	Human		name
598233250	CV3929733	single nucleotide variant	NM_001080529.3(WIPF3):c.1448G>A (p.Arg483Gln)	not specified [RCV005295538]	uncertain significance	7	29914512	29914512	Human		name
598267252	CV3929735	single nucleotide variant	NM_001080529.3(WIPF3):c.1061C>T (p.Ser354Phe)	not specified [RCV005302137]	uncertain significance	7	29884555	29884555	Human		name
15177641	CV700029	single nucleotide variant	NM_001080529.3(WIPF3):c.1105G>A (p.Gly369Ser)	not provided [RCV000951090]	benign	7	29888073	29888073	Human		name

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