Rnf6 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 Rnf6

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15170183	CV744695	single nucleotide variant	NM_005977.4(RNF6):c.193+6A>C	not provided [RCV000905212]	likely benign	13	26219451	26219451	Human		name
597688461	CV3590576	single nucleotide variant	NM_005977.4(RNF6):c.26A>G (p.Asp9Gly)	not specified [RCV004858604]	uncertain significance	13	26219624	26219624	Human		name
598206441	CV3909833	single nucleotide variant	NM_005977.4(RNF6):c.16T>C (p.Ser6Pro)	not specified [RCV005269852]	uncertain significance	13	26219634	26219634	Human		name
15119762	CV753768	single nucleotide variant	NM_005977.4(RNF6):c.249A>G (p.Leu83=)	not provided [RCV000918198]	benign	13	26218551	26218551	Human		name
407513482	CV3479785	single nucleotide variant	NM_005977.4(RNF6):c.67C>T (p.His23Tyr)	not specified [RCV004674139]	uncertain significance	13	26219583	26219583	Human		name
407513489	CV3479789	single nucleotide variant	NM_005977.4(RNF6):c.65A>C (p.His22Pro)	not specified [RCV004674142]	uncertain significance	13	26219585	26219585	Human		name
156169627	CV2337378	single nucleotide variant	NM_005977.4(RNF6):c.235G>A (p.Val79Ile)	not specified [RCV004187823]	uncertain significance	13	26218565	26218565	Human		name
407486890	CV3479781	single nucleotide variant	NM_005977.4(RNF6):c.173A>G (p.His58Arg)	not specified [RCV004665537]	uncertain significance	13	26219477	26219477	Human		name
597755499	CV3590579	single nucleotide variant	NM_005977.4(RNF6):c.270A>C (p.Arg90Ser)	not specified [RCV004847630]	uncertain significance	13	26218530	26218530	Human		name
597688502	CV3590583	single nucleotide variant	NM_005977.4(RNF6):c.236T>C (p.Val79Ala)	not specified [RCV004858608]	uncertain significance	13	26218564	26218564	Human		name
597755507	CV3590585	single nucleotide variant	NM_005977.4(RNF6):c.188C>T (p.Thr63Ile)	not specified [RCV004847632]	uncertain significance	13	26219462	26219462	Human		name
598206456	CV3909836	single nucleotide variant	NM_005977.4(RNF6):c.134A>G (p.Asn45Ser)	not specified [RCV005269855]	uncertain significance	13	26219516	26219516	Human		name
15170175	CV739008	single nucleotide variant	NM_005977.4(RNF6):c.1089A>G (p.Ala363=)	not provided [RCV000905211]	benign	13	26214793	26214793	Human		name
8596883	CV20739	single nucleotide variant	NM_005977.4(RNF6):c.305G>A (p.Arg102Lys)	Esophageal squamous cell carcinoma, somatic [RCV000006054]	pathogenic\|other	13	26215577	26215577	Human	1	name
8596884	CV20740	single nucleotide variant	NM_005977.4(RNF6):c.724G>A (p.Ala242Thr)	Esophageal squamous cell carcinoma, somatic [RCV000006055]	pathogenic\|other	13	26215158	26215158	Human	1	name
8596885	CV20741	single nucleotide variant	NM_005977.4(RNF6):c.731G>A (p.Gly244Asp)	Esophageal squamous cell carcinoma, somatic [RCV000006056]	pathogenic\|other	13	26215151	26215151	Human	1	name
156202321	CV2234484	single nucleotide variant	NM_005977.4(RNF6):c.755G>A (p.Arg252His)	not specified [RCV004100687]	likely benign	13	26215127	26215127	Human		name
156211984	CV2259920	single nucleotide variant	NM_005977.4(RNF6):c.442C>T (p.Arg148Trp)	not specified [RCV004118951]	uncertain significance	13	26215440	26215440	Human		name
156117918	CV2278937	single nucleotide variant	NM_005977.4(RNF6):c.608T>C (p.Val203Ala)	not specified [RCV004145630]	uncertain significance	13	26215274	26215274	Human		name
156192581	CV2289433	single nucleotide variant	NM_005977.4(RNF6):c.820C>T (p.Arg274Trp)	not specified [RCV004152386]	uncertain significance	13	26215062	26215062	Human		name
156396285	CV2326194	single nucleotide variant	NM_005977.4(RNF6):c.592A>G (p.Arg198Gly)	not specified [RCV004180462]	uncertain significance	13	26215290	26215290	Human		name
329362193	CV2448395	single nucleotide variant	NM_005977.4(RNF6):c.957T>G (p.Ser319Arg)	not specified [RCV004256680]	uncertain significance	13	26214925	26214925	Human		name
329364181	CV2467263	single nucleotide variant	NM_005977.4(RNF6):c.352C>T (p.Arg118Trp)	not specified [RCV004285072]	uncertain significance	13	26215530	26215530	Human		name
401751407	CV2716377	single nucleotide variant	NM_005977.4(RNF6):c.962C>G (p.Thr321Ser)	not specified [RCV004325370]	uncertain significance	13	26214920	26214920	Human		name
401725352	CV2721734	single nucleotide variant	NM_005977.4(RNF6):c.865G>A (p.Val289Ile)	not specified [RCV004324475]	uncertain significance	13	26215017	26215017	Human		name
405699167	CV3309527	single nucleotide variant	NM_005977.4(RNF6):c.698G>C (p.Gly233Ala)	not specified [RCV004446795]	uncertain significance	13	26215184	26215184	Human		name
405699173	CV3309528	single nucleotide variant	NM_005977.4(RNF6):c.730G>A (p.Gly244Ser)	not specified [RCV004446796]	uncertain significance	13	26215152	26215152	Human		name
405699180	CV3309529	single nucleotide variant	NM_005977.4(RNF6):c.923A>G (p.Asn308Ser)	not specified [RCV004446797]	likely benign	13	26214959	26214959	Human		name
405699184	CV3309530	single nucleotide variant	NM_005977.4(RNF6):c.959G>A (p.Gly320Asp)	not specified [RCV004446798]	uncertain significance	13	26214923	26214923	Human		name
407486900	CV3479783	single nucleotide variant	NM_005977.4(RNF6):c.542A>G (p.His181Arg)	not specified [RCV004665539]	uncertain significance	13	26215340	26215340	Human		name
597755495	CV3590578	single nucleotide variant	NM_005977.4(RNF6):c.659G>T (p.Arg220Met)	not specified [RCV004847629]	uncertain significance	13	26215223	26215223	Human		name
598206436	CV3909832	single nucleotide variant	NM_005977.4(RNF6):c.587G>A (p.Arg196Gln)	not specified [RCV005269851]	uncertain significance	13	26215295	26215295	Human		name
598206451	CV3909835	single nucleotide variant	NM_005977.4(RNF6):c.860G>A (p.Ser287Asn)	not specified [RCV005269854]	uncertain significance	13	26215022	26215022	Human		name
15196286	CV725432	single nucleotide variant	NM_005977.4(RNF6):c.568A>G (p.Thr190Ala)	not provided [RCV000889735]	likely benign	13	26215314	26215314	Human		name
8627429	CV82573	single nucleotide variant	NM_005977.3(RNF6):c.868A>T (p.Thr290Ser)	Malignant melanoma [RCV000062652]	not provided	13	26215014	26215014	Human		name
155923989	CV2212526	single nucleotide variant	NM_005977.4(RNF6):c.1139A>G (p.Glu380Gly)	not specified [RCV004091409]	uncertain significance	13	26214743	26214743	Human		name
156063021	CV2277326	single nucleotide variant	NM_005977.4(RNF6):c.1328G>A (p.Arg443Gln)	not specified [RCV004142935]	uncertain significance	13	26214554	26214554	Human		name
156300747	CV2306994	single nucleotide variant	NM_005977.4(RNF6):c.1375A>G (p.Thr459Ala)	not specified [RCV004157501]	uncertain significance	13	26214507	26214507	Human		name
156272151	CV2308755	single nucleotide variant	NM_005977.4(RNF6):c.1361G>A (p.Arg454Gln)	not specified [RCV004169076]	uncertain significance	13	26214521	26214521	Human		name
156042464	CV2342229	single nucleotide variant	NM_005977.4(RNF6):c.1021G>C (p.Val341Leu)	not specified [RCV004191808]	uncertain significance	13	26214861	26214861	Human		name
156105896	CV2361351	single nucleotide variant	NM_005977.4(RNF6):c.1664C>A (p.Thr555Asn)	not specified [RCV004218554]	uncertain significance	13	26214218	26214218	Human		name
155995924	CV2393122	single nucleotide variant	NM_005977.4(RNF6):c.1699G>A (p.Gly567Ser)	not specified [RCV004226602]	uncertain significance	13	26214183	26214183	Human		name
401780737	CV2727540	single nucleotide variant	NM_005977.4(RNF6):c.1759C>T (p.Arg587Cys)	not specified [RCV004329732]	uncertain significance	13	26214123	26214123	Human		name
401862712	CV2778974	single nucleotide variant	NM_005977.4(RNF6):c.1502A>G (p.Asp501Gly)	not specified [RCV004348632]	uncertain significance	13	26214380	26214380	Human		name
405699500	CV3309522	single nucleotide variant	NM_005977.4(RNF6):c.1241G>A (p.Arg414Gln)	not specified [RCV004446790]	uncertain significance	13	26214641	26214641	Human		name
405699496	CV3309523	single nucleotide variant	NM_005977.4(RNF6):c.1241G>C (p.Arg414Pro)	not specified [RCV004446791]	uncertain significance	13	26214641	26214641	Human		name
405699493	CV3309524	single nucleotide variant	NM_005977.4(RNF6):c.1682G>A (p.Arg561Gln)	not specified [RCV004446792]	uncertain significance	13	26214200	26214200	Human		name
405699303	CV3309525	single nucleotide variant	NM_005977.4(RNF6):c.1756C>G (p.Leu586Val)	not specified [RCV004446793]	uncertain significance	13	26214126	26214126	Human		name
405699162	CV3309526	single nucleotide variant	NM_005977.4(RNF6):c.2041A>C (p.Ile681Leu)	not specified [RCV004446794]	uncertain significance	13	26213841	26213841	Human		name
407486885	CV3479780	single nucleotide variant	NM_005977.4(RNF6):c.1760G>A (p.Arg587His)	not specified [RCV004665536]	uncertain significance	13	26214122	26214122	Human		name
407486894	CV3479782	single nucleotide variant	NM_005977.4(RNF6):c.1811G>A (p.Arg604His)	not specified [RCV004665538]	uncertain significance	13	26214071	26214071	Human		name
407513479	CV3479784	single nucleotide variant	NM_005977.4(RNF6):c.1378A>G (p.Ile460Val)	not specified [RCV004674138]	uncertain significance	13	26214504	26214504	Human		name
407486905	CV3479786	single nucleotide variant	NM_005977.4(RNF6):c.1672C>T (p.Pro558Ser)	not specified [RCV004665540]	uncertain significance	13	26214210	26214210	Human		name
407513485	CV3479787	single nucleotide variant	NM_005977.4(RNF6):c.1247G>C (p.Ser416Thr)	not specified [RCV004674140]	uncertain significance	13	26214635	26214635	Human		name
407513488	CV3479788	single nucleotide variant	NM_005977.4(RNF6):c.1587G>C (p.Arg529Ser)	not specified [RCV004674141]	uncertain significance	13	26214295	26214295	Human		name
597688441	CV3590573	single nucleotide variant	NM_005977.4(RNF6):c.1681C>G (p.Arg561Gly)	not specified [RCV004858602]	likely benign	13	26214201	26214201	Human		name
597688452	CV3590574	single nucleotide variant	NM_005977.4(RNF6):c.1534C>T (p.His512Tyr)	not specified [RCV004858603]	uncertain significance	13	26214348	26214348	Human		name
597755491	CV3590575	single nucleotide variant	NM_005977.4(RNF6):c.1175G>A (p.Arg392Gln)	not specified [RCV004847628]	uncertain significance	13	26214707	26214707	Human		name
597688481	CV3590580	single nucleotide variant	NM_005977.4(RNF6):c.1906A>G (p.Ile636Val)	not specified [RCV004858606]	uncertain significance	13	26213976	26213976	Human		name
597688491	CV3590581	single nucleotide variant	NM_005977.4(RNF6):c.1577A>G (p.Asp526Gly)	not specified [RCV004858607]	uncertain significance	13	26214305	26214305	Human		name
597755503	CV3590582	single nucleotide variant	NM_005977.4(RNF6):c.1622A>G (p.Gln541Arg)	not specified [RCV004847631]	uncertain significance	13	26214260	26214260	Human		name
597688511	CV3590584	single nucleotide variant	NM_005977.4(RNF6):c.1115T>C (p.Leu372Pro)	not specified [RCV004858609]	uncertain significance	13	26214767	26214767	Human		name
597755511	CV3590586	single nucleotide variant	NM_005977.4(RNF6):c.2018G>A (p.Arg673Gln)	not specified [RCV004847633]	uncertain significance	13	26213864	26213864	Human		name
598206467	CV3905947	single nucleotide variant	NM_005977.4(RNF6):c.1463T>C (p.Met488Thr)	not specified [RCV005269857]	uncertain significance	13	26214419	26214419	Human		name
598206432	CV3909831	single nucleotide variant	NM_005977.4(RNF6):c.1207G>A (p.Val403Met)	not specified [RCV005269850]	uncertain significance	13	26214675	26214675	Human		name
598206461	CV3909837	single nucleotide variant	NM_005977.4(RNF6):c.1165A>G (p.Thr389Ala)	not specified [RCV005269856]	likely benign	13	26214717	26214717	Human		name
15186176	CV725431	single nucleotide variant	NM_005977.4(RNF6):c.1715G>A (p.Arg572Gln)	not provided [RCV000886903]	benign	13	26214167	26214167	Human		name
15161340	CV739007	single nucleotide variant	NM_005977.4(RNF6):c.1625C>A (p.Ala542Asp)	not provided [RCV000903328]	likely benign	13	26214257	26214257	Human		name

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