Wfdc1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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90 records found for search term Wfdc1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597739719	CV3630180	single nucleotide variant	NM_021197.4(WFDC1):c.4C>G (p.Pro2Ala)	not specified [RCV004890386]	uncertain significance	16	84294975	84294975	Human		name
15153484	CV755432	single nucleotide variant	NM_021197.4(WFDC1):c.81C>T (p.His27=)	not provided [RCV000924068]	likely benign	16	84295052	84295052	Human		name
155918853	CV2333081	single nucleotide variant	NM_021197.4(WFDC1):c.16G>A (p.Val6Met)	not provided [RCV004695597]\|not specified [RCV004194376]	uncertain significance	16	84294987	84294987	Human		name
15097938	CV726835	single nucleotide variant	NM_021197.4(WFDC1):c.13G>A (p.Gly5Ser)	not provided [RCV000891619]	likely benign	16	84294984	84294984	Human		name
15199349	CV755433	single nucleotide variant	NM_021197.4(WFDC1):c.168C>A (p.Gly56=)	not provided [RCV000912521]	likely benign	16	84312984	84312984	Human		name
401774081	CV2727726	single nucleotide variant	NM_021197.4(WFDC1):c.32G>A (p.Cys11Tyr)	not specified [RCV004323763]	uncertain significance	16	84295003	84295003	Human		name
401728824	CV2729834	single nucleotide variant	NM_021197.4(WFDC1):c.85G>A (p.Gly29Ser)	not specified [RCV004332841]	likely benign	16	84295056	84295056	Human		name
401877345	CV2769422	single nucleotide variant	NM_021197.4(WFDC1):c.53C>T (p.Ala18Val)	not specified [RCV004357407]	uncertain significance	16	84295024	84295024	Human		name
407524456	CV3490014	single nucleotide variant	NM_021197.4(WFDC1):c.82G>A (p.Ala28Thr)	not specified [RCV004678430]	uncertain significance	16	84295053	84295053	Human		name
407524471	CV3490020	single nucleotide variant	NM_021197.4(WFDC1):c.36G>C (p.Arg12Ser)	not specified [RCV004678435]	uncertain significance	16	84295007	84295007	Human		name
597792212	CV3630178	single nucleotide variant	NM_021197.4(WFDC1):c.76C>T (p.Leu26Phe)	not specified [RCV004876918]	uncertain significance	16	84295047	84295047	Human		name
155962919	CV2308210	single nucleotide variant	NM_021197.4(WFDC1):c.119C>T (p.Pro40Leu)	not specified [RCV004164711]	uncertain significance	16	84295090	84295090	Human		name
156077889	CV2318631	single nucleotide variant	NM_021197.4(WFDC1):c.256G>A (p.Asp86Asn)	not specified [RCV004173530]	uncertain significance	16	84313072	84313072	Human		name
401744153	CV2696946	single nucleotide variant	NM_021197.4(WFDC1):c.268C>G (p.Pro90Ala)	not specified [RCV004292941]	uncertain significance	16	84313084	84313084	Human		name
401779328	CV2718498	single nucleotide variant	NM_021197.4(WFDC1):c.110G>A (p.Arg37Gln)	not specified [RCV004318305]	uncertain significance	16	84295081	84295081	Human		name
401867513	CV2766701	single nucleotide variant	NM_021197.4(WFDC1):c.136A>G (p.Lys46Glu)	not specified [RCV004347308]	uncertain significance	16	84295107	84295107	Human		name
405807797	CV3356626	single nucleotide variant	NM_021197.4(WFDC1):c.176G>A (p.Arg59Gln)	not specified [RCV004480886]	uncertain significance	16	84312992	84312992	Human		name
405807799	CV3356627	single nucleotide variant	NM_021197.4(WFDC1):c.263A>C (p.Glu88Ala)	not specified [RCV004480887]	uncertain significance	16	84313079	84313079	Human		name
407524468	CV3490018	single nucleotide variant	NM_021197.4(WFDC1):c.294C>G (p.Asn98Lys)	not specified [RCV004678434]	uncertain significance	16	84313110	84313110	Human		name
407465423	CV3490019	single nucleotide variant	NM_021197.4(WFDC1):c.277C>T (p.Arg93Trp)	not specified [RCV004688764]	uncertain significance	16	84313093	84313093	Human		name
597739714	CV3630176	single nucleotide variant	NM_021197.4(WFDC1):c.185G>A (p.Arg62Gln)	not specified [RCV004890385]	uncertain significance	16	84313001	84313001	Human		name
597792215	CV3630179	single nucleotide variant	NM_021197.4(WFDC1):c.266G>T (p.Cys89Phe)	not specified [RCV004876919]	uncertain significance	16	84313082	84313082	Human		name
597739723	CV3630181	single nucleotide variant	NM_021197.4(WFDC1):c.227G>A (p.Gly76Asp)	not specified [RCV004890387]	uncertain significance	16	84313043	84313043	Human		name
598233036	CV3933561	single nucleotide variant	NM_021197.4(WFDC1):c.254C>T (p.Ala85Val)	not specified [RCV005295505]	uncertain significance	16	84313070	84313070	Human		name
598267131	CV3933563	single nucleotide variant	NM_021197.4(WFDC1):c.175C>T (p.Arg59Trp)	not specified [RCV005302106]	uncertain significance	16	84312991	84312991	Human		name
156366556	CV2203351	single nucleotide variant	NM_021197.4(WFDC1):c.601C>T (p.Pro201Ser)	not specified [RCV004072581]	uncertain significance	16	84324457	84324457	Human		name
156270744	CV2315605	single nucleotide variant	NM_021197.4(WFDC1):c.503G>A (p.Gly168Asp)	not specified [RCV004169641]	uncertain significance	16	84319512	84319512	Human		name
156159207	CV2361484	single nucleotide variant	NM_021197.4(WFDC1):c.332C>A (p.Pro111Gln)	not specified [RCV004221123]	uncertain significance	16	84313148	84313148	Human		name
401769864	CV2718922	single nucleotide variant	NM_021197.4(WFDC1):c.518G>T (p.Gly173Val)	not specified [RCV004322522]	uncertain significance	16	84319527	84319527	Human		name
401889652	CV2758358	single nucleotide variant	NM_021197.4(WFDC1):c.553C>G (p.Arg185Gly)	not specified [RCV004341707]	uncertain significance	16	84319562	84319562	Human		name
401873087	CV2793198	single nucleotide variant	NM_021197.4(WFDC1):c.473C>T (p.Ser158Leu)	not specified [RCV004360503]	uncertain significance	16	84319482	84319482	Human		name
405807801	CV3356628	single nucleotide variant	NM_021197.4(WFDC1):c.380G>T (p.Gly127Val)	not specified [RCV004480888]	uncertain significance	16	84318314	84318314	Human		name
405807803	CV3356629	single nucleotide variant	NM_021197.4(WFDC1):c.385G>T (p.Gly129Cys)	not specified [RCV004480889]	uncertain significance	16	84318319	84318319	Human		name
405807805	CV3356630	single nucleotide variant	NM_021197.4(WFDC1):c.481G>A (p.Glu161Lys)	not specified [RCV004480890]	uncertain significance	16	84319490	84319490	Human		name
407524462	CV3490016	single nucleotide variant	NM_021197.4(WFDC1):c.578G>A (p.Arg193Gln)	not specified [RCV004678432]	uncertain significance	16	84324434	84324434	Human		name
407524465	CV3490017	single nucleotide variant	NM_021197.4(WFDC1):c.491T>C (p.Ile164Thr)	not specified [RCV004678433]	uncertain significance	16	84319500	84319500	Human		name
597792208	CV3630177	single nucleotide variant	NM_021197.4(WFDC1):c.359C>T (p.Pro120Leu)	not specified [RCV004876917]	uncertain significance	16	84318293	84318293	Human		name
598267127	CV3933560	single nucleotide variant	NM_021197.4(WFDC1):c.514G>A (p.Glu172Lys)	not specified [RCV005302105]	uncertain significance	16	84319523	84319523	Human		name
598233042	CV3933562	single nucleotide variant	NM_021197.4(WFDC1):c.630A>T (p.Glu210Asp)	not specified [RCV005295506]	uncertain significance	16	84326907	84326907	Human		name
15191362	CV703855	single nucleotide variant	NM_021197.4(WFDC1):c.412G>A (p.Val138Met)	not provided [RCV000954753]	benign	16	84318346	84318346	Human		name
15103544	CV726836	single nucleotide variant	NM_021197.4(WFDC1):c.541G>A (p.Val181Ile)	not provided [RCV000892698]	benign	16	84319550	84319550	Human		name
15190780	CV726837	single nucleotide variant	NM_021197.4(WFDC1):c.586C>G (p.Leu196Val)	not provided [RCV000888195]	benign	16	84324442	84324442	Human		name
15196417	CV755434	single nucleotide variant	NM_021197.4(WFDC1):c.577C>T (p.Arg193Ter)	not provided [RCV000911691]	likely benign	16	84324433	84324433	Human		name
401758771	CV2705121	single nucleotide variant	NM_172006.2(WFDC10B):c.-133G>A	not specified [RCV004310024]	uncertain significance	20	45704921	45704921	Human		name
405807813	CV3356634	single nucleotide variant	NM_172006.2(WFDC10B):c.-178G>A	not specified [RCV004480894]	uncertain significance	20	45704966	45704966	Human		name
401765146	CV2712501	single nucleotide variant	NM_080869.2(WFDC12):c.5G>T (p.Gly2Val)	not specified [RCV004307847]	uncertain significance	20	45124443	45124443	Human		name
156146540	CV2218935	single nucleotide variant	NM_172005.2(WFDC13):c.14T>G (p.Leu5Arg)	not specified [RCV004087120]	uncertain significance	20	45702137	45702137	Human		name
156238606	CV2285901	single nucleotide variant	NM_147197.2(WFDC11):c.25A>G (p.Ile9Val)	not specified [RCV004143831]	uncertain significance	20	45650576	45650576	Human		name
15114571	CV717006	single nucleotide variant	NM_172005.2(WFDC13):c.111C>T (p.Pro37=)	not provided [RCV000961700]	benign	20	45704466	45704466	Human		name
8637324	CV92550	single nucleotide variant	NM_080869.1(WFDC12):c.231G>A (p.Leu77=)	Malignant melanoma [RCV000072648]	not provided	20	45124114	45124114	Human		name
156400881	CV2217362	single nucleotide variant	NM_080753.3(WFDC10A):c.13A>G (p.Thr5Ala)	Inborn genetic diseases [RCV002656719]	likely benign	20	45629826	45629826	Human	1	name
156175468	CV2254663	single nucleotide variant	NM_080869.2(WFDC12):c.68G>T (p.Gly23Val)	not specified [RCV004115150]	uncertain significance	20	45124380	45124380	Human		name
156294746	CV2293238	single nucleotide variant	NM_172005.2(WFDC13):c.95T>A (p.Ile32Asn)	not specified [RCV004150741]	uncertain significance	20	45704450	45704450	Human		name
329390660	CV2440302	single nucleotide variant	NM_080869.2(WFDC12):c.95G>A (p.Gly32Glu)	not specified [RCV004262783]	uncertain significance	20	45124250	45124250	Human		name
401781511	CV2726546	single nucleotide variant	NM_080869.2(WFDC12):c.31G>T (p.Val11Leu)	not specified [RCV004328726]	uncertain significance	20	45124417	45124417	Human		name
405807816	CV3356636	single nucleotide variant	NM_172005.2(WFDC13):c.79C>T (p.Arg27Cys)	not specified [RCV004480896]	uncertain significance	20	45702202	45702202	Human		name
405807818	CV3356637	single nucleotide variant	NM_172005.2(WFDC13):c.82G>A (p.Val28Ile)	not specified [RCV004480897]	uncertain significance	20	45702205	45702205	Human		name
407524473	CV3490022	single nucleotide variant	NM_147197.2(WFDC11):c.32T>C (p.Met11Thr)	not specified [RCV004678437]	uncertain significance	20	45650569	45650569	Human		name
407524476	CV3490023	single nucleotide variant	NM_080869.2(WFDC12):c.78G>T (p.Glu26Asp)	not specified [RCV004678438]	uncertain significance	20	45124370	45124370	Human		name
597792220	CV3630184	single nucleotide variant	NM_147197.2(WFDC11):c.55G>A (p.Val19Met)	not specified [RCV004876921]	uncertain significance	20	45650546	45650546	Human		name
597792233	CV3630190	single nucleotide variant	NM_172005.2(WFDC13):c.80G>A (p.Arg27His)	not specified [RCV004876925]	likely benign	20	45702203	45702203	Human		name
156115797	CV2273429	single nucleotide variant	NM_147197.2(WFDC11):c.196T>C (p.Tyr66His)	not specified [RCV004132187]	likely benign	20	45649304	45649304	Human		name
156267294	CV2329665	single nucleotide variant	NM_080753.3(WFDC10A):c.78G>C (p.Lys26Asn)	not specified [RCV004180777]	uncertain significance	20	45629891	45629891	Human		name
156019052	CV2370385	single nucleotide variant	NM_147197.2(WFDC11):c.248C>T (p.Thr83Ile)	not specified [RCV004213283]	uncertain significance	20	45648735	45648735	Human		name
329358767	CV2425368	single nucleotide variant	NM_080869.2(WFDC12):c.269C>T (p.Pro90Leu)	not specified [RCV004251029]	uncertain significance	20	45123913	45123913	Human		name
329360570	CV2439508	single nucleotide variant	NM_080753.3(WFDC10A):c.73G>A (p.Asp25Asn)	not specified [RCV004262447]	uncertain significance	20	45629886	45629886	Human		name
329401084	CV2446098	single nucleotide variant	NM_080753.3(WFDC10A):c.81G>C (p.Lys27Asn)	not specified [RCV004270654]	uncertain significance	20	45629894	45629894	Human		name
329395774	CV2454553	single nucleotide variant	NM_147197.2(WFDC11):c.235A>G (p.Ile79Val)	not specified [RCV004268037]	uncertain significance	20	45649265	45649265	Human		name
401758752	CV2705110	single nucleotide variant	NM_080753.3(WFDC10A):c.55G>T (p.Ala19Ser)	not specified [RCV004310014]	uncertain significance	20	45629868	45629868	Human		name
401884302	CV2761653	single nucleotide variant	NM_080869.2(WFDC12):c.217C>G (p.Pro73Ala)	not specified [RCV004337273]	uncertain significance	20	45124128	45124128	Human		name
405807814	CV3356635	single nucleotide variant	NM_172005.2(WFDC13):c.205G>A (p.Val69Ile)	not specified [RCV004480895]	uncertain significance	20	45704560	45704560	Human		name
407524479	CV3490024	single nucleotide variant	NM_080869.2(WFDC12):c.234A>C (p.Glu78Asp)	not specified [RCV004678439]	uncertain significance	20	45124111	45124111	Human		name
597792226	CV3630187	single nucleotide variant	NM_080869.2(WFDC12):c.266G>T (p.Arg89Met)	not specified [RCV004876923]	uncertain significance	20	45123916	45123916	Human		name
597739738	CV3630188	single nucleotide variant	NM_080869.2(WFDC12):c.205A>G (p.Lys69Glu)	not specified [RCV004890390]	uncertain significance	20	45124140	45124140	Human		name
597792229	CV3630189	single nucleotide variant	NM_080869.2(WFDC12):c.160G>A (p.Asp54Asn)	not specified [RCV004876924]	uncertain significance	20	45124185	45124185	Human		name
597792235	CV3630191	single nucleotide variant	NM_172005.2(WFDC13):c.278A>C (p.Asn93Thr)	not specified [RCV004876926]	uncertain significance	20	45705901	45705901	Human		name
598267144	CV3933566	single nucleotide variant	NM_147197.2(WFDC11):c.161A>C (p.Lys54Thr)	not specified [RCV005302109]	uncertain significance	20	45649339	45649339	Human		name
598267148	CV3933567	single nucleotide variant	NM_147197.2(WFDC11):c.244G>A (p.Glu82Lys)	not specified [RCV005302110]	likely benign	20	45648739	45648739	Human		name
156326516	CV2205780	single nucleotide variant	NM_080753.3(WFDC10A):c.185C>A (p.Ala62Glu)	not specified [RCV004599443]	uncertain significance	20	45630963	45630963	Human		name
155976255	CV2266277	single nucleotide variant	NM_080753.3(WFDC10A):c.193A>G (p.Ile65Val)	not specified [RCV004129110]	uncertain significance	20	45630971	45630971	Human		name
156244382	CV2267364	single nucleotide variant	NM_080869.2(WFDC12):c.331A>G (p.Lys111Glu)	not specified [RCV004134021]	uncertain significance	20	45123851	45123851	Human		name
329352429	CV2453009	single nucleotide variant	NM_080753.3(WFDC10A):c.155A>T (p.His52Leu)	not specified [RCV004277629]	uncertain significance	20	45630933	45630933	Human		name
405807809	CV3356632	single nucleotide variant	NM_080753.3(WFDC10A):c.119T>A (p.Val40Asp)	not specified [RCV004480892]	uncertain significance	20	45630897	45630897	Human		name
405807978	CV3356633	single nucleotide variant	NM_172006.2(WFDC10B):c.103T>C (p.Cys35Arg)	not specified [RCV004480893]	uncertain significance	20	45684949	45684949	Human		name
407487896	CV3490021	single nucleotide variant	NM_080753.3(WFDC10A):c.117A>C (p.Lys39Asn)	not specified [RCV004678436]	uncertain significance	20	45630895	45630895	Human		name
597792217	CV3630182	single nucleotide variant	NM_080753.3(WFDC10A):c.199T>C (p.Cys67Arg)	not specified [RCV004876920]	uncertain significance	20	45630977	45630977	Human		name
597739726	CV3630183	single nucleotide variant	NM_172006.2(WFDC10B):c.124G>T (p.Asp42Tyr)	not specified [RCV004890388]	uncertain significance	20	45684928	45684928	Human		name
597792223	CV3630185	single nucleotide variant	NM_080869.2(WFDC12):c.308C>T (p.Ser103Phe)	not specified [RCV004876922]	uncertain significance	20	45123874	45123874	Human		name
597739731	CV3630186	single nucleotide variant	NM_080869.2(WFDC12):c.311C>T (p.Ser104Phe)	not specified [RCV004890389]	uncertain significance	20	45123871	45123871	Human		name
598267140	CV3933565	single nucleotide variant	NM_172006.2(WFDC10B):c.113G>A (p.Arg38Gln)	not specified [RCV005302108]	uncertain significance	20	45684939	45684939	Human		name

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