Rnh1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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60 records found for search term Rnh1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401796942	CV2740110	single nucleotide variant	NM_203387.3(RNH1):c.615-2A>C	Encephalitis, acute, infection-induced, susceptibility to, 12 [RCV003320404]	risk factor	11	498935	498935	Human	1	name
15198859	CV777953	single nucleotide variant	NM_203387.3(RNH1):c.444-10T>C	not provided [RCV000956879]	benign	11	499195	499195	Human		name
598206626	CV3905977	single nucleotide variant	NM_203387.3(RNH1):c.213C>T (p.Val71=)	not specified [RCV005269887]	likely benign	11	500543	500543	Human		name
156171640	CV2198028	single nucleotide variant	NM_203387.3(RNH1):c.49G>A (p.Asp17Asn)	not specified [RCV004077231]	uncertain significance	11	502114	502114	Human		name
156341827	CV2268318	single nucleotide variant	NM_203387.3(RNH1):c.73C>T (p.Pro25Ser)	not specified [RCV004138606]	uncertain significance	11	502090	502090	Human		name
155989407	CV2282718	single nucleotide variant	NM_203387.3(RNH1):c.94G>A (p.Val32Met)	not specified [RCV004141583]	uncertain significance	11	502069	502069	Human		name
401770164	CV2710943	single nucleotide variant	NM_203387.3(RNH1):c.97G>A (p.Val33Ile)	not specified [RCV004310659]	uncertain significance	11	502066	502066	Human		name
401796946	CV2740115	single nucleotide variant	NM_203387.3(RNH1):c.40G>T (p.Glu14Ter)	Encephalitis, acute, infection-induced, susceptibility to, 12 [RCV003320407]	risk factor	11	502123	502123	Human	1	name
401903985	CV2806367	single nucleotide variant	NM_203387.3(RNH1):c.981C>T (p.Ala327=)	not provided [RCV003394661]	likely benign	11	498117	498117	Human		name
156272164	CV2308756	single nucleotide variant	NM_203387.3(RNH1):c.280A>C (p.Asn94His)	not specified [RCV004169077]	uncertain significance	11	499992	499992	Human		name
401796943	CV2740112	single nucleotide variant	NM_203387.3(RNH1):c.279G>T (p.Gln93His)	Encephalitis, acute, infection-induced, susceptibility to, 12 [RCV003320405]	risk factor	11	499993	499993	Human	1	name
597755593	CV3586730	single nucleotide variant	NM_203387.3(RNH1):c.293C>T (p.Thr98Met)	not specified [RCV004847652]	uncertain significance	11	499979	499979	Human		name
598206631	CV3905978	single nucleotide variant	NM_203387.3(RNH1):c.181C>A (p.Leu61Ile)	not specified [RCV005269888]	uncertain significance	11	500575	500575	Human		name
156398628	CV2194690	single nucleotide variant	NM_203387.3(RNH1):c.833G>A (p.Arg278His)	not specified [RCV004075249]	uncertain significance	11	498580	498580	Human		name
156044207	CV2215912	single nucleotide variant	NM_203387.3(RNH1):c.734C>T (p.Ala245Val)	not specified [RCV004096993]	uncertain significance	11	498814	498814	Human		name
156016144	CV2266268	single nucleotide variant	NM_203387.3(RNH1):c.580C>G (p.Leu194Val)	not specified [RCV004129101]	uncertain significance	11	499049	499049	Human		name
156083088	CV2301217	single nucleotide variant	NM_203387.3(RNH1):c.436A>G (p.Lys146Glu)	not specified [RCV004160121]	uncertain significance	11	499836	499836	Human		name
155967301	CV2329901	single nucleotide variant	NM_203387.3(RNH1):c.740T>C (p.Leu247Pro)	not specified [RCV004183356]	uncertain significance	11	498808	498808	Human		name
329368993	CV2424719	single nucleotide variant	NM_203387.3(RNH1):c.307G>A (p.Gly103Arg)	not specified [RCV004248613]	uncertain significance	11	499965	499965	Human		name
329370022	CV2424918	single nucleotide variant	NM_203387.3(RNH1):c.626G>A (p.Cys209Tyr)	Encephalitis, acute, infection-induced, susceptibility to, 12 [RCV003320395]\|not specified [RCV004248794]	risk factor\|uncertain significance	11	498922	498922	Human	1	name
401774347	CV2691703	single nucleotide variant	NM_203387.3(RNH1):c.548A>G (p.Asn183Ser)	not specified [RCV004299165]	uncertain significance	11	499081	499081	Human		name
401735672	CV2695373	single nucleotide variant	NM_203387.3(RNH1):c.541G>T (p.Asp181Tyr)	not specified [RCV004305581]	uncertain significance	11	499088	499088	Human		name
401796944	CV2740113	single nucleotide variant	NM_203387.3(RNH1):c.887T>C (p.Leu296Pro)	Encephalitis, acute, infection-induced, susceptibility to, 12 [RCV003320406]	risk factor	11	498526	498526	Human	1	name
405699407	CV3309568	single nucleotide variant	NM_203387.3(RNH1):c.394C>G (p.Leu132Val)	not specified [RCV004446836]	uncertain significance	11	499878	499878	Human		name
405699419	CV3309570	single nucleotide variant	NM_203387.3(RNH1):c.623G>A (p.Ser208Asn)	not specified [RCV004446838]	likely benign	11	498925	498925	Human		name
405699428	CV3309571	single nucleotide variant	NM_203387.3(RNH1):c.661G>A (p.Gly221Ser)	not specified [RCV004446839]	likely benign	11	498887	498887	Human		name
405699433	CV3309572	single nucleotide variant	NM_203387.3(RNH1):c.815G>A (p.Gly272Asp)	not specified [RCV004446840]	uncertain significance	11	498598	498598	Human		name
405699438	CV3309573	single nucleotide variant	NM_203387.3(RNH1):c.860A>C (p.Lys287Thr)	not specified [RCV004446841]	uncertain significance	11	498553	498553	Human		name
405699447	CV3309575	single nucleotide variant	NM_203387.3(RNH1):c.982G>A (p.Ala328Thr)	not specified [RCV004446843]	uncertain significance	11	498116	498116	Human		name
407513495	CV3479805	single nucleotide variant	NM_203387.3(RNH1):c.527C>T (p.Thr176Met)	not specified [RCV004674146]	uncertain significance	11	499102	499102	Human		name
407486986	CV3479806	single nucleotide variant	NM_203387.3(RNH1):c.829T>C (p.Cys277Arg)	not specified [RCV004665553]	uncertain significance	11	498584	498584	Human		name
407486992	CV3479807	single nucleotide variant	NM_203387.3(RNH1):c.628G>T (p.Gly210Cys)	not specified [RCV004665554]	uncertain significance	11	498920	498920	Human		name
407486997	CV3479808	single nucleotide variant	NM_203387.3(RNH1):c.364G>A (p.Asp122Asn)	not specified [RCV004665555]	uncertain significance	11	499908	499908	Human		name
597755602	CV3586735	single nucleotide variant	NM_203387.3(RNH1):c.478G>A (p.Glu160Lys)	not specified [RCV004847654]	uncertain significance	11	499151	499151	Human		name
597755606	CV3586736	single nucleotide variant	NM_203387.3(RNH1):c.514T>A (p.Phe172Ile)	not specified [RCV004847655]	uncertain significance	11	499115	499115	Human		name
597688693	CV3586739	single nucleotide variant	NM_203387.3(RNH1):c.553G>T (p.Ala185Ser)	not specified [RCV004858628]	uncertain significance	11	499076	499076	Human		name
598206592	CV3905971	single nucleotide variant	NM_203387.3(RNH1):c.628G>A (p.Gly210Ser)	not specified [RCV005269881]	uncertain significance	11	498920	498920	Human		name
598206597	CV3905972	single nucleotide variant	NM_203387.3(RNH1):c.821G>A (p.Gly274Glu)	not specified [RCV005269882]	uncertain significance	11	498592	498592	Human		name
598206608	CV3905974	single nucleotide variant	NM_203387.3(RNH1):c.383C>T (p.Ala128Val)	not specified [RCV005269884]	uncertain significance	11	499889	499889	Human		name
598206621	CV3905976	single nucleotide variant	NM_203387.3(RNH1):c.652G>A (p.Asp218Asn)	not specified [RCV005269886]	uncertain significance	11	498896	498896	Human		name
598206636	CV3905979	single nucleotide variant	NM_203387.3(RNH1):c.665T>C (p.Ile222Thr)	not specified [RCV005269889]	uncertain significance	11	498883	498883	Human		name
156060057	CV2284400	single nucleotide variant	NM_203387.3(RNH1):c.1178C>T (p.Thr393Ile)	not specified [RCV004146738]	uncertain significance	11	495003	495003	Human		name
155967199	CV2329888	single nucleotide variant	NM_203387.3(RNH1):c.1096G>A (p.Gly366Ser)	not specified [RCV004183346]	uncertain significance	11	498002	498002	Human		name
156363703	CV2330014	single nucleotide variant	NM_203387.3(RNH1):c.1103C>T (p.Pro368Leu)	not specified [RCV004185507]	uncertain significance	11	497995	497995	Human		name
156171706	CV2400708	single nucleotide variant	NM_203387.3(RNH1):c.1075C>T (p.Arg359Trp)	not specified [RCV004242379]	uncertain significance	11	498023	498023	Human		name
329391288	CV2452211	single nucleotide variant	NM_203387.3(RNH1):c.1336C>T (p.Arg446Trp)	not specified [RCV004278912]	uncertain significance	11	494741	494741	Human		name
329351950	CV2455521	single nucleotide variant	NM_203387.3(RNH1):c.1214T>C (p.Leu405Pro)	not specified [RCV004276784]	uncertain significance	11	494967	494967	Human		name
401757888	CV2685617	single nucleotide variant	NM_203387.3(RNH1):c.1223A>G (p.Asn408Ser)	not specified [RCV004294626]	uncertain significance	11	494958	494958	Human		name
405699390	CV3309565	single nucleotide variant	NM_203387.3(RNH1):c.1076G>A (p.Arg359Gln)	not specified [RCV004446833]	likely benign	11	498022	498022	Human		name
405699396	CV3309566	single nucleotide variant	NM_203387.3(RNH1):c.1236C>A (p.Asp412Glu)	not specified [RCV004446834]	uncertain significance	11	494945	494945	Human		name
405699400	CV3309567	single nucleotide variant	NM_203387.3(RNH1):c.1256T>C (p.Val419Ala)	not specified [RCV004446835]	uncertain significance	11	494925	494925	Human		name
407487003	CV3479809	single nucleotide variant	NM_203387.3(RNH1):c.1336C>G (p.Arg446Gly)	not specified [RCV004665556]	uncertain significance	11	494741	494741	Human		name
597688652	CV3586733	single nucleotide variant	NM_203387.3(RNH1):c.1237G>A (p.Ala413Thr)	not specified [RCV004858624]	uncertain significance	11	494944	494944	Human		name
597688659	CV3586734	single nucleotide variant	NM_203387.3(RNH1):c.1238C>T (p.Ala413Val)	not specified [RCV004858625]	uncertain significance	11	494943	494943	Human		name
597688670	CV3586737	single nucleotide variant	NM_203387.3(RNH1):c.1130T>G (p.Leu377Trp)	not specified [RCV004858626]	uncertain significance	11	495051	495051	Human		name
597688683	CV3586738	single nucleotide variant	NM_203387.3(RNH1):c.1306G>A (p.Asp436Asn)	not specified [RCV004858627]	uncertain significance	11	494771	494771	Human		name
597755610	CV3586740	single nucleotide variant	NM_203387.3(RNH1):c.1274C>A (p.Pro425Gln)	not specified [RCV004847656]	uncertain significance	11	494907	494907	Human		name
598206602	CV3905973	single nucleotide variant	NM_203387.3(RNH1):c.1067C>G (p.Ala356Gly)	not specified [RCV005269883]	uncertain significance	11	498031	498031	Human		name
40904109	CV976589	single nucleotide variant	NM_203387.3(RNH1):c.1117C>T (p.Arg373Trp)	Encephalitis, acute, infection-induced, susceptibility to, 12 [RCV003320374]\|RNH1-related disorder [RCV001270361]	risk factor\|uncertain significance	11	497981	497981	Human	1	name , trait , alternate_id
40904108	CV976590	indel	NM_203387.3(RNH1):c.682_685delinsCTGGGCCTTGGGCA (p.Ser228fs)	Encephalitis, acute, infection-induced, susceptibility to, 12 [RCV003320373]\|RNH1-related disorder [RCV001270360]	risk factor\|uncertain significance	11	498863	498866	Human		name , trait , alternate_id

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