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71 records found for search term Snx13
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15178047CV779324single nucleotide variantNM_015132.5(SNX13):c.440+10C>Tnot provided [RCV000973570]benign71789035317890353Humanname
155972607CV2309425single nucleotide variantNM_015132.5(SNX13):c.64A>G (p.Ile22Val)not specified [RCV004165567]likely benign71789739517897395Humanname
12896766CV390597duplicationNM_015132.5(SNX13):c.1954-22_1954-21dupnot specified [RCV000455793]benign71781495217814953Humanname
156122470CV2241102single nucleotide variantNM_015132.5(SNX13):c.163T>A (p.Ser55Thr)not specified [RCV004104138]uncertain significance71789339717893397Humanname
156103430CV2313745single nucleotide variantNM_015132.5(SNX13):c.218G>A (p.Gly73Glu)not specified [RCV004157657]uncertain significance71789334217893342Humanname
401781969CV2722366single nucleotide variantNM_015132.5(SNX13):c.158C>G (p.Thr53Arg)not specified [RCV004322775]uncertain significance71789340217893402Humanname
401769564CV2731417single nucleotide variantNM_015132.5(SNX13):c.237A>C (p.Glu79Asp)not specified [RCV004330779]uncertain significance71789162717891627Humanname
401925611CV2828327single nucleotide variantNM_015132.5(SNX13):c.1152A>G (p.Leu384=)not provided [RCV003436663]likely benign71784560817845608Humanname
401925612CV2828328single nucleotide variantNM_015132.5(SNX13):c.1110C>T (p.Cys370=)not provided [RCV003436664]likely benign71784565017845650Humanname
597745249CV3607240single nucleotide variantNM_015132.5(SNX13):c.293A>G (p.Asn98Ser)not specified [RCV004865633]uncertain significance71789157117891571Humanname
598171848CV3911658single nucleotide variantNM_015132.5(SNX13):c.259A>G (p.Thr87Ala)not specified [RCV005284893]uncertain significance71789160517891605Humanname
15172351CV722440single nucleotide variantNM_015132.5(SNX13):c.1254A>G (p.Glu418=)not provided [RCV000883824]benign71783991217839912Humanname
155919479CV2202627single nucleotide variantNM_015132.5(SNX13):c.523G>A (p.Ala175Thr)not specified [RCV004082883]uncertain significance71787570817875708Humanname
156200484CV2237709single nucleotide variantNM_015132.5(SNX13):c.653A>G (p.Lys218Arg)not specified [RCV004100500]uncertain significance71787549117875491Humanname
156113024CV2387977single nucleotide variantNM_015132.5(SNX13):c.882T>G (p.Ile294Met)not specified [RCV004236512]uncertain significance71785092017850920Humanname
329351957CV2455527single nucleotide variantNM_015132.5(SNX13):c.766C>G (p.Arg256Gly)not specified [RCV004276789]uncertain significance71786847817868478Humanname
401763229CV2707598single nucleotide variantNM_015132.5(SNX13):c.839T>C (p.Ile280Thr)not specified [RCV004306539]uncertain significance71785096317850963Humanname
401770036CV2719005single nucleotide variantNM_015132.5(SNX13):c.895A>G (p.Asn299Asp)not specified [RCV004322592]uncertain significance71785090717850907Humanname
401883567CV2757991single nucleotide variantNM_015132.5(SNX13):c.547G>A (p.Asp183Asn)not specified [RCV004339164]uncertain significance71787568417875684Humanname
401868793CV2767344single nucleotide variantNM_015132.5(SNX13):c.775C>A (p.Leu259Ile)not specified [RCV004349506]uncertain significance71786846917868469Humanname
401893941CV2773583single nucleotide variantNM_015132.5(SNX13):c.778C>T (p.Leu260Phe)not specified [RCV004355989]uncertain significance71786846617868466Humanname
401896065CV2777389single nucleotide variantNM_015132.5(SNX13):c.740G>A (p.Arg247Gln)not specified [RCV004354392]uncertain significance71787354117873541Humanname
405732432CV3322550single nucleotide variantNM_015132.5(SNX13):c.508C>G (p.Arg170Gly)not specified [RCV004464512]uncertain significance71787572317875723Humanname
405732442CV3322551single nucleotide variantNM_015132.5(SNX13):c.548A>G (p.Asp183Gly)not specified [RCV004464513]uncertain significance71787568317875683Humanname
407503817CV3484779single nucleotide variantNM_015132.5(SNX13):c.541G>A (p.Glu181Lys)not specified [RCV004670375]uncertain significance71787569017875690Humanname
597745233CV3607236single nucleotide variantNM_015132.5(SNX13):c.848C>T (p.Ser283Phe)not specified [RCV004865630]uncertain significance71785095417850954Humanname
597741027CV3607239single nucleotide variantNM_015132.5(SNX13):c.889A>T (p.Ser297Cys)not specified [RCV004864777]uncertain significance71785091317850913Humanname
598171843CV3911659single nucleotide variantNM_015132.5(SNX13):c.617A>G (p.Lys206Arg)not specified [RCV005284894]uncertain significance71787552717875527Humanname
156268387CV2198899single nucleotide variantNM_015132.5(SNX13):c.1453A>G (p.Ile485Val)not specified [RCV004077932]uncertain significance71783477217834772Humanname
156228101CV2199380single nucleotide variantNM_015132.5(SNX13):c.2572A>T (p.Ile858Phe)not specified [RCV004070953]uncertain significance71779688117796881Humanname
155969634CV2244604single nucleotide variantNM_015132.5(SNX13):c.2240T>C (p.Ile747Thr)not specified [RCV004102326]uncertain significance71780164617801646Humanname
156137069CV2280560single nucleotide variantNM_015132.5(SNX13):c.2293G>A (p.Asp765Asn)not specified [RCV004143046]uncertain significance71780159317801593Humanname
156242578CV2283202single nucleotide variantNM_015132.5(SNX13):c.2776C>T (p.Arg926Cys)not specified [RCV004145880]uncertain significance71779414317794143Humanname
156141805CV2288585single nucleotide variantNM_015132.5(SNX13):c.1412C>G (p.Thr471Ser)not specified [RCV004152105]uncertain significance71783481317834813Humanname
155997112CV2288586single nucleotide variantNM_015132.5(SNX13):c.2817G>A (p.Met939Ile)not specified [RCV004152106]uncertain significance71779410217794102Humanname
156352447CV2323973single nucleotide variantNM_015132.5(SNX13):c.1798C>T (p.Arg600Cys)not specified [RCV004176493]uncertain significance71782155617821556Humanname
155927124CV2345341single nucleotide variantNM_015132.5(SNX13):c.2119G>T (p.Val707Phe)not specified [RCV004198121]uncertain significance71780352617803526Humanname
156146933CV2357972single nucleotide variantNM_015132.5(SNX13):c.1460G>A (p.Arg487Lys)not specified [RCV004209752]uncertain significance71783476517834765Humanname
155937844CV2364926single nucleotide variantNM_015132.5(SNX13):c.2840A>C (p.Gln947Pro)not specified [RCV004222222]uncertain significance71779407917794079Humanname
401728213CV2676012single nucleotide variantNM_015132.5(SNX13):c.2576G>A (p.Arg859Gln)not specified [RCV004282002]uncertain significance71779687717796877Humanname
401757447CV2693007single nucleotide variantNM_015132.5(SNX13):c.1098T>G (p.Phe366Leu)not specified [RCV004306512]uncertain significance71784566217845662Humanname
401748296CV2698342single nucleotide variantNM_015132.5(SNX13):c.1757A>T (p.His586Leu)not specified [RCV004304884]uncertain significance71782159717821597Humanname
401730614CV2711416single nucleotide variantNM_015132.5(SNX13):c.1412C>T (p.Thr471Ile)not specified [RCV004313168]uncertain significance71783481317834813Humanname
401784295CV2721241single nucleotide variantNM_015132.5(SNX13):c.1382A>G (p.Asp461Gly)not specified [RCV004330181]uncertain significance71783484317834843Humanname
401856977CV2759910single nucleotide variantNM_015132.5(SNX13):c.2105A>C (p.Asn702Thr)not specified [RCV004345336]uncertain significance71780354017803540Humanname
401893745CV2762033single nucleotide variantNM_015132.5(SNX13):c.1888A>G (p.Thr630Ala)not specified [RCV004341854]uncertain significance71781624717816247Humanname
401892284CV2776046single nucleotide variantNM_015132.5(SNX13):c.2248A>G (p.Thr750Ala)not specified [RCV004353152]uncertain significance71780163817801638Humanname
401876029CV2789270single nucleotide variantNM_015132.5(SNX13):c.2788A>G (p.Asn930Asp)not specified [RCV004365299]uncertain significance71779413117794131Humanname
405732341CV3322539single nucleotide variantNM_015132.5(SNX13):c.1090G>C (p.Ala364Pro)not specified [RCV004464501]uncertain significance71784567017845670Humanname
405732348CV3322540single nucleotide variantNM_015132.5(SNX13):c.1268G>A (p.Arg423His)not specified [RCV004464502]uncertain significance71783989817839898Humanname
405732356CV3322541single nucleotide variantNM_015132.5(SNX13):c.1418A>G (p.Asn473Ser)not specified [RCV004464503]uncertain significance71783480717834807Humanname
405732365CV3322542single nucleotide variantNM_015132.5(SNX13):c.1531C>T (p.Arg511Cys)not specified [RCV004464504]uncertain significance71783411817834118Humanname
405732376CV3322543single nucleotide variantNM_015132.5(SNX13):c.1719T>A (p.Asp573Glu)not specified [RCV004464505]uncertain significance71782163517821635Humanname
405732385CV3322544single nucleotide variantNM_015132.5(SNX13):c.1762C>T (p.Arg588Cys)not specified [RCV004464506]uncertain significance71782159217821592Humanname
405732393CV3322545single nucleotide variantNM_015132.5(SNX13):c.1982C>T (p.Ala661Val)not specified [RCV004464507]uncertain significance71781491617814916Humanname
405732403CV3322546single nucleotide variantNM_015132.5(SNX13):c.2138G>A (p.Ser713Asn)not specified [RCV004464508]uncertain significance71780350717803507Humanname
405732409CV3322547single nucleotide variantNM_015132.5(SNX13):c.2645T>C (p.Ile882Thr)not specified [RCV004464509]uncertain significance71779427417794274Humanname
405732416CV3322548single nucleotide variantNM_015132.5(SNX13):c.2731T>C (p.Phe911Leu)not specified [RCV004464510]uncertain significance71779418817794188Humanname
405732427CV3322549single nucleotide variantNM_015132.5(SNX13):c.2740G>A (p.Gly914Ser)not specified [RCV004464511]uncertain significance71779417917794179Humanname
407503820CV3484780single nucleotide variantNM_015132.5(SNX13):c.1580C>T (p.Ser527Phe)not specified [RCV004670376]uncertain significance71783406917834069Humanname
407525301CV3484781single nucleotide variantNM_015132.5(SNX13):c.1629A>G (p.Ile543Met)not specified [RCV004679123]uncertain significance71783001617830016Humanname
407503825CV3484782single nucleotide variantNM_015132.5(SNX13):c.1108T>G (p.Cys370Gly)not specified [RCV004670377]uncertain significance71784565217845652Humanname
597741021CV3607233single nucleotide variantNM_015132.5(SNX13):c.2215T>C (p.Ser739Pro)not specified [RCV004864776]uncertain significance71780343017803430Humanname
597745222CV3607234single nucleotide variantNM_015132.5(SNX13):c.1657G>A (p.Val553Ile)not specified [RCV004865628]uncertain significance71782607017826070Humanname
597745227CV3607235single nucleotide variantNM_015132.5(SNX13):c.1217T>C (p.Val406Ala)not specified [RCV004865629]uncertain significance71783994917839949Humanname
597745239CV3607237single nucleotide variantNM_015132.5(SNX13):c.1479G>A (p.Met493Ile)not specified [RCV004865631]uncertain significance71783417017834170Humanname
597745244CV3607238single nucleotide variantNM_015132.5(SNX13):c.1585G>A (p.Asp529Asn)not specified [RCV004865632]uncertain significance71783406417834064Humanname
597745259CV3607242single nucleotide variantNM_015132.5(SNX13):c.1181C>G (p.Thr394Ser)not specified [RCV004865635]uncertain significance71783998517839985Humanname
598171858CV3911656single nucleotide variantNM_015132.5(SNX13):c.2761C>T (p.Pro921Ser)not specified [RCV005284891]uncertain significance71779415817794158Humanname
598171853CV3911657single nucleotide variantNM_015132.5(SNX13):c.1484G>T (p.Arg495Leu)not specified [RCV005284892]uncertain significance71783416517834165Humanname
598171838CV3911660single nucleotide variantNM_015132.5(SNX13):c.1187G>T (p.Gly396Val)not specified [RCV005284895]uncertain significance71783997917839979Humanname