Spns1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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40 records found for search term Spns1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401903118	CV2807772	single nucleotide variant	NM_032038.3(SPNS1):c.981C>A (p.Leu327=)	not provided [RCV003419270]	likely benign	16	28982371	28982371	Human		name
401911567	CV2807773	single nucleotide variant	NM_032038.3(SPNS1):c.996C>T (p.Thr332=)	not provided [RCV003426646]	likely benign	16	28982386	28982386	Human		name
598263303	CV3919341	single nucleotide variant	NM_032038.3(SPNS1):c.438C>T (p.Pro146=)	not specified [RCV005280477]	likely benign	16	28978038	28978038	Human		name
405737076	CV3323338	single nucleotide variant	NM_032038.3(SPNS1):c.200A>G (p.Tyr67Cys)	not specified [RCV004465110]	uncertain significance	16	28975351	28975351	Human		name
407525685	CV3477934	single nucleotide variant	NM_032038.3(SPNS1):c.112G>A (p.Glu38Lys)	not specified [RCV004679386]	uncertain significance	16	28975263	28975263	Human		name
407511517	CV3477936	single nucleotide variant	NM_032038.3(SPNS1):c.101C>T (p.Pro34Leu)	not specified [RCV004673126]	uncertain significance	16	28975252	28975252	Human		name
407511523	CV3477938	single nucleotide variant	NM_032038.3(SPNS1):c.114G>T (p.Glu38Asp)	not specified [RCV004673128]	likely benign	16	28975265	28975265	Human		name
598239134	CV3919342	single nucleotide variant	NM_032038.3(SPNS1):c.146G>C (p.Arg49Pro)	not specified [RCV005275954]	uncertain significance	16	28975297	28975297	Human		name
15192647	CV703610	single nucleotide variant	NM_032038.3(SPNS1):c.1425C>T (p.Gly475=)	not provided [RCV000955134]	benign	16	28983890	28983890	Human		name
156171961	CV2194179	single nucleotide variant	NM_032038.3(SPNS1):c.742C>T (p.Arg248Cys)	not specified [RCV004077265]	uncertain significance	16	28981548	28981548	Human		name
156023576	CV2233486	single nucleotide variant	NM_032038.3(SPNS1):c.375G>T (p.Lys125Asn)	not specified [RCV004106105]	uncertain significance	16	28977975	28977975	Human		name
155964091	CV2261570	single nucleotide variant	NM_032038.3(SPNS1):c.875T>C (p.Leu292Pro)	not specified [RCV004125902]	uncertain significance	16	28981966	28981966	Human		name
156118605	CV2279084	single nucleotide variant	NM_032038.3(SPNS1):c.818T>A (p.Phe273Tyr)	not specified [RCV004145758]	uncertain significance	16	28981909	28981909	Human		name
156060601	CV2391902	single nucleotide variant	NM_032038.3(SPNS1):c.439G>A (p.Gly147Arg)	not specified [RCV004235770]	likely benign	16	28978039	28978039	Human		name
329375909	CV2441197	single nucleotide variant	NM_032038.3(SPNS1):c.636G>C (p.Met212Ile)	not specified [RCV004263593]	uncertain significance	16	28979444	28979444	Human		name
407511515	CV3477935	single nucleotide variant	NM_032038.3(SPNS1):c.947C>T (p.Ser316Phe)	not specified [RCV004673125]	uncertain significance	16	28982038	28982038	Human		name
597678907	CV3607684	single nucleotide variant	NM_032038.3(SPNS1):c.905G>A (p.Arg302His)	not specified [RCV004857245]	uncertain significance	16	28981996	28981996	Human		name
597678914	CV3607686	single nucleotide variant	NM_032038.3(SPNS1):c.728G>A (p.Arg243Lys)	not specified [RCV004857246]	uncertain significance	16	28981534	28981534	Human		name
598263309	CV3915455	single nucleotide variant	NM_032038.3(SPNS1):c.967C>G (p.Leu323Val)	not specified [RCV005280479]	uncertain significance	16	28982357	28982357	Human		name
598263312	CV3915456	single nucleotide variant	NM_032038.3(SPNS1):c.794G>A (p.Arg265Lys)	not specified [RCV005280480]	uncertain significance	16	28981600	28981600	Human		name
598263301	CV3919340	single nucleotide variant	NM_032038.3(SPNS1):c.554G>T (p.Ser185Ile)	not specified [RCV005280476]	uncertain significance	16	28979264	28979264	Human		name
156316135	CV2193012	single nucleotide variant	NM_032038.3(SPNS1):c.1567G>A (p.Val523Met)	not specified [RCV004069563]	uncertain significance	16	28984279	28984279	Human		name
156377723	CV2211419	single nucleotide variant	NM_032038.3(SPNS1):c.1472G>A (p.Arg491Gln)	not specified [RCV004090327]	uncertain significance	16	28983937	28983937	Human		name
156329295	CV2213810	single nucleotide variant	NM_032038.3(SPNS1):c.1210G>A (p.Asp404Asn)	not specified [RCV004089870]	uncertain significance	16	28982911	28982911	Human		name
155961778	CV2285574	single nucleotide variant	NM_032038.3(SPNS1):c.1060G>A (p.Ala354Thr)	not specified [RCV004141448]	uncertain significance	16	28982450	28982450	Human		name
156291957	CV2296738	single nucleotide variant	NM_032038.3(SPNS1):c.1313T>C (p.Ile438Thr)	not specified [RCV004148644]	uncertain significance	16	28983283	28983283	Human		name
156345880	CV2308933	single nucleotide variant	NM_032038.3(SPNS1):c.1362G>T (p.Leu454Phe)	not specified [RCV004169221]	uncertain significance	16	28983827	28983827	Human		name
156195793	CV2347594	single nucleotide variant	NM_032038.3(SPNS1):c.1549C>T (p.Arg517Cys)	not specified [RCV004200532]	uncertain significance	16	28984261	28984261	Human		name
156103227	CV2352353	single nucleotide variant	NM_032038.3(SPNS1):c.1012G>A (p.Gly338Ser)	not specified [RCV004200823]	uncertain significance	16	28982402	28982402	Human		name
329395676	CV2454458	single nucleotide variant	NM_032038.3(SPNS1):c.1504G>A (p.Glu502Lys)	not specified [RCV004267961]	uncertain significance	16	28984216	28984216	Human		name
401725503	CV2735894	single nucleotide variant	NM_032038.3(SPNS1):c.1550G>A (p.Arg517His)	not provided [RCV003312337]	likely benign	16	28984262	28984262	Human		name
405737060	CV3323336	single nucleotide variant	NM_032038.3(SPNS1):c.1207G>T (p.Ala403Ser)	not specified [RCV004465108]	uncertain significance	16	28982908	28982908	Human		name
405737067	CV3323337	single nucleotide variant	NM_032038.3(SPNS1):c.1561G>A (p.Val521Met)	not specified [RCV004465109]	uncertain significance	16	28984273	28984273	Human		name
407511512	CV3477933	single nucleotide variant	NM_032038.3(SPNS1):c.1402G>A (p.Ala468Thr)	not specified [RCV004673124]	uncertain significance	16	28983867	28983867	Human		name
407511521	CV3477937	single nucleotide variant	NM_032038.3(SPNS1):c.1486G>A (p.Val496Met)	not specified [RCV004673127]	uncertain significance	16	28983951	28983951	Human		name
597768879	CV3607681	single nucleotide variant	NM_032038.3(SPNS1):c.1525C>T (p.Arg509Trp)	not specified [RCV004871127]	uncertain significance	16	28984237	28984237	Human		name
597768884	CV3607682	single nucleotide variant	NM_032038.3(SPNS1):c.1340G>A (p.Arg447Gln)	not specified [RCV004871128]	uncertain significance	16	28983805	28983805	Human		name
597768889	CV3607683	single nucleotide variant	NM_032038.3(SPNS1):c.1047C>G (p.His349Gln)	not specified [RCV004871129]	uncertain significance	16	28982437	28982437	Human		name
597768894	CV3607685	single nucleotide variant	NM_032038.3(SPNS1):c.1393A>G (p.Met465Val)	not specified [RCV004871130]	uncertain significance	16	28983858	28983858	Human		name
598263305	CV3919343	single nucleotide variant	NM_032038.3(SPNS1):c.1034G>A (p.Arg345His)	not specified [RCV005280478]	uncertain significance	16	28982424	28982424	Human		name

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