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Variants search result for Homo sapiens
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36 records found for search term Stau1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15165056CV778579single nucleotide variantNM_017453.4(STAU1):c.344+9T>Gnot provided [RCV000948497]benign204915392449153924Humanname
8586514CV121117single nucleotide variantNM_017453.2(STAU1):c.206-4672C>ALung cancer [RCV000101637]uncertain significance204915874349158743Humanname
329359512CV2446300single nucleotide variantNM_017453.4(STAU1):c.52A>C (p.Ser18Arg)not specified [RCV004249434]uncertain significance204916615049166150Humanname
598251113CV3919536single nucleotide variantNM_017453.4(STAU1):c.30C>G (p.Asn10Lys)not specified [RCV005277825]uncertain significance204916617249166172Humanname
156299404CV2310729single nucleotide variantNM_017453.4(STAU1):c.115A>G (p.Thr39Ala)not specified [RCV004157378]likely benign204916608749166087Humanname
329354768CV2449017single nucleotide variantNM_017453.4(STAU1):c.296T>C (p.Met99Thr)not specified [RCV004264094]uncertain significance204915398149153981Humanname
597747156CV3618546single nucleotide variantNM_017453.4(STAU1):c.188C>T (p.Ser63Phe)not specified [RCV004866011]uncertain significance204916601449166014Humanname
598251108CV3919535single nucleotide variantNM_017453.4(STAU1):c.127C>T (p.Pro43Ser)not specified [RCV005277824]uncertain significance204916607549166075Humanname
156056988CV2308968single nucleotide variantNM_017453.4(STAU1):c.302C>A (p.Ser101Tyr)not specified [RCV004169250]uncertain significance204915397549153975Humanname
156104602CV2386972single nucleotide variantNM_017453.4(STAU1):c.337C>T (p.Pro113Ser)not specified [RCV004226729]uncertain significance204915394049153940Humanname
329400315CV2441488single nucleotide variantNM_017453.4(STAU1):c.832A>C (p.Ser278Arg)not specified [RCV004257282]uncertain significance204912322649123226Humanname
401758437CV2694102single nucleotide variantNM_017453.4(STAU1):c.935G>C (p.Gly312Ala)not specified [RCV004302534]uncertain significance204912312349123123Humanname
405739808CV3334322single nucleotide variantNM_017453.4(STAU1):c.545A>G (p.Asn182Ser)not specified [RCV004465535]uncertain significance204913589749135897Humanname
405739816CV3334323single nucleotide variantNM_017453.4(STAU1):c.657G>C (p.Lys219Asn)not specified [RCV004465536]uncertain significance204912454049124540Humanname
407530102CV3485406single nucleotide variantNM_017453.4(STAU1):c.586C>T (p.Arg196Trp)not specified [RCV004681643]uncertain significance204913585649135856Humanname
407530103CV3485407single nucleotide variantNM_017453.4(STAU1):c.850G>A (p.Gly284Arg)not specified [RCV004681644]uncertain significance204912320849123208Humanname
407496098CV3485408single nucleotide variantNM_017453.4(STAU1):c.637A>T (p.Met213Leu)not specified [RCV004668037]uncertain significance204912456049124560Humanname
407496101CV3485409single nucleotide variantNM_017453.4(STAU1):c.308A>C (p.Tyr103Ser)not specified [RCV004668038]uncertain significance204915396949153969Humanname
597747172CV3618550single nucleotide variantNM_017453.4(STAU1):c.305C>T (p.Thr102Ile)not specified [RCV004866014]uncertain significance204915397249153972Humanname
598251120CV3919537single nucleotide variantNM_017453.4(STAU1):c.490C>T (p.Pro164Ser)not specified [RCV005277826]uncertain significance204915160249151602Humanname
156129645CV2279704single nucleotide variantNM_017453.4(STAU1):c.1070C>T (p.Pro357Leu)not specified [RCV004144324]uncertain significance204912002549120025Humanname
156179857CV2298407single nucleotide variantNM_017453.4(STAU1):c.1637C>T (p.Ala546Val)not specified [RCV004162081]uncertain significance204911586349115863Humanname
156079531CV2300931single nucleotide variantNM_017453.4(STAU1):c.1316T>C (p.Phe439Ser)not specified [RCV004158118]uncertain significance204911797049117970Humanname
156245118CV2347213single nucleotide variantNM_017453.4(STAU1):c.1411A>G (p.Ile471Val)not specified [RCV004204684]uncertain significance204911787549117875Humanname
156246371CV2347307single nucleotide variantNM_017453.4(STAU1):c.1028A>C (p.Asn343Thr)not specified [RCV004206786]uncertain significance204912006749120067Humanname
155968785CV2391500single nucleotide variantNM_017453.4(STAU1):c.1448A>G (p.His483Arg)not specified [RCV004239886]uncertain significance204911783849117838Humanname
329375977CV2466326single nucleotide variantNM_017453.4(STAU1):c.1360A>T (p.Met454Leu)not specified [RCV004280246]uncertain significance204911792649117926Humanname
401729565CV2690342single nucleotide variantNM_017453.4(STAU1):c.1346C>A (p.Ala449Asp)not specified [RCV004302338]uncertain significance204911794049117940Humanname
597747151CV3618545single nucleotide variantNM_017453.4(STAU1):c.1331C>T (p.Pro444Leu)not specified [RCV004866010]uncertain significance204911795549117955Humanname
597747162CV3618547single nucleotide variantNM_017453.4(STAU1):c.1590C>G (p.Ile530Met)not specified [RCV004866012]uncertain significance204911716849117168Humanname
597747167CV3618548single nucleotide variantNM_017453.4(STAU1):c.1465C>T (p.Pro489Ser)not specified [RCV004866013]uncertain significance204911782149117821Humanname
597703548CV3618549single nucleotide variantNM_017453.4(STAU1):c.1592G>T (p.Ser531Ile)not specified [RCV004860205]uncertain significance204911716649117166Humanname
598251090CV3919532single nucleotide variantNM_017453.4(STAU1):c.1024C>T (p.Arg342Cys)not specified [RCV005277821]uncertain significance204912007149120071Humanname
598251096CV3919533single nucleotide variantNM_017453.4(STAU1):c.1459A>G (p.Thr487Ala)not specified [RCV005277822]uncertain significance204911782749117827Humanname
598251101CV3919534single nucleotide variantNM_017453.4(STAU1):c.1684G>A (p.Glu562Lys)not specified [RCV005277823]uncertain significance204911581649115816Humanname
598213806CV3919538single nucleotide variantNM_017453.4(STAU1):c.1165G>A (p.Gly389Ser)not specified [RCV005271107]uncertain significance204911835749118357Humanname