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Variants search result for Homo sapiens
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33 records found for search term Gjb5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155930861CV2220926single nucleotide variantNM_005268.4(GJB5):c.26T>C (p.Leu9Pro)not specified [RCV004092625]uncertain significance13475735634757356Humanname
156189063CV2395601single nucleotide variantNM_005268.4(GJB5):c.64C>T (p.Arg22Cys)not specified [RCV004241450]uncertain significance13475739434757394Humanname
401750042CV2695916single nucleotide variantNM_005268.4(GJB5):c.88A>G (p.Ile30Val)not specified [RCV004308191]uncertain significance13475741834757418Humanname
405737373CV3254988single nucleotide variantNM_005268.4(GJB5):c.83T>C (p.Val28Ala)not specified [RCV004390806]uncertain significance13475741334757413Humanname
155992156CV2255786single nucleotide variantNM_005268.4(GJB5):c.199G>A (p.Glu67Lys)not specified [RCV004120161]uncertain significance13475752934757529Humanname
155916665CV2282207single nucleotide variantNM_005268.4(GJB5):c.292C>T (p.Arg98Trp)not specified [RCV004132789]uncertain significance13475762234757622Humanname
156056502CV2371089single nucleotide variantNM_005268.4(GJB5):c.224G>A (p.Arg75His)not specified [RCV004220842]uncertain significance13475755434757554Humanname
405737354CV3254985single nucleotide variantNM_005268.4(GJB5):c.125G>A (p.Arg42His)not specified [RCV004390803]uncertain significance13475745534757455Humanname
597759521CV3684607single nucleotide variantNM_005268.4(GJB5):c.124C>T (p.Arg42Cys)not specified [RCV004925522]uncertain significance13475745434757454Humanname
597707198CV3684608single nucleotide variantNM_005268.4(GJB5):c.148G>A (p.Asp50Asn)not specified [RCV004917068]uncertain significance13475747834757478Humanname
598220617CV3977718single nucleotide variantNM_005268.4(GJB5):c.271G>A (p.Val91Met)not specified [RCV005340480]uncertain significance13475760134757601Humanname
598251835CV3977722single nucleotide variantNM_005268.4(GJB5):c.164C>G (p.Thr55Ser)not specified [RCV005345978]uncertain significance13475749434757494Humanname
156368906CV2193818single nucleotide variantNM_005268.4(GJB5):c.788G>A (p.Arg263His)not specified [RCV004074568]likely benign13475811834758118Humanname
156120288CV2219335single nucleotide variantNM_005268.4(GJB5):c.512A>G (p.Asn171Ser)not specified [RCV004095180]uncertain significance13475784234757842Humanname
156065323CV2287318single nucleotide variantNM_005268.4(GJB5):c.420C>A (p.Ser140Arg)not specified [RCV004146943]uncertain significance13475775034757750Humanname
156293702CV2293096single nucleotide variantNM_005268.4(GJB5):c.548A>G (p.Lys183Arg)not specified [RCV004148836]uncertain significance13475787834757878Humanname
155973313CV2332389single nucleotide variantNM_005268.4(GJB5):c.421G>A (p.Val141Met)not specified [RCV004196121]uncertain significance13475775134757751Humanname
329386588CV2428339single nucleotide variantNM_005268.4(GJB5):c.365A>G (p.Lys122Arg)not specified [RCV004251361]uncertain significance13475769534757695Humanname
329352090CV2452009single nucleotide variantNM_005268.4(GJB5):c.362G>T (p.Gly121Val)not specified [RCV004278746]uncertain significance13475769234757692Humanname
329351812CV2455340single nucleotide variantNM_005268.4(GJB5):c.767A>G (p.His256Arg)not specified [RCV004274842]uncertain significance13475809734758097Humanname
401772332CV2712672single nucleotide variantNM_005268.4(GJB5):c.787C>T (p.Arg263Cys)not specified [RCV004307989]uncertain significance13475811734758117Humanname
401887673CV2772082single nucleotide variantNM_005268.4(GJB5):c.491G>A (p.Cys164Tyr)not specified [RCV004344748]uncertain significance13475782134757821Humanname
401869391CV2772385single nucleotide variantNM_005268.4(GJB5):c.310A>G (p.Arg104Gly)not specified [RCV004355182]uncertain significance13475764034757640Humanname
405737367CV3254987single nucleotide variantNM_005268.4(GJB5):c.586A>G (p.Ile196Val)not specified [RCV004390805]likely benign13475791634757916Humanname
407513310CV3443269single nucleotide variantNM_005268.4(GJB5):c.370C>T (p.Arg124Trp)not specified [RCV004627136]uncertain significance13475770034757700Humanname
407503898CV3443270single nucleotide variantNM_005268.4(GJB5):c.607G>A (p.Val203Met)not specified [RCV004623895]uncertain significance13475793734757937Humanname
407513312CV3443271single nucleotide variantNM_005268.4(GJB5):c.674T>C (p.Met225Thr)not specified [RCV004627137]likely benign13475800434758004Humanname
407513314CV3443272single nucleotide variantNM_005268.4(GJB5):c.563T>G (p.Leu188Arg)not specified [RCV004627138]uncertain significance13475789334757893Humanname
597707179CV3684605single nucleotide variantNM_005268.4(GJB5):c.725A>T (p.Asp242Val)not specified [RCV004917066]uncertain significance13475805534758055Humanname
597707190CV3684606single nucleotide variantNM_005268.4(GJB5):c.361G>A (p.Gly121Ser)not specified [RCV004917067]uncertain significance13475769134757691Humanname
598251820CV3977719single nucleotide variantNM_005268.4(GJB5):c.416C>T (p.Ala139Val)not specified [RCV005345975]uncertain significance13475774634757746Humanname
598251825CV3977720single nucleotide variantNM_005268.4(GJB5):c.724G>A (p.Asp242Asn)not specified [RCV005345976]uncertain significance13475805434758054Humanname
598251830CV3977721single nucleotide variantNM_005268.4(GJB5):c.773C>A (p.Pro258His)not specified [RCV005345977]uncertain significance13475810334758103Humanname