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Variants search result for Homo sapiens
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27 records found for search term Herpud1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329355667CV2445568single nucleotide variantNM_014685.4(HERPUD1):c.22G>A (p.Glu8Lys)not specified [RCV004257611]uncertain significance165693226656932266Humanname
597761063CV3685614single nucleotide variantNM_014685.4(HERPUD1):c.28G>A (p.Val10Ile)not specified [RCV004925827]uncertain significance165693227256932272Humanname
156159793CV2361648single nucleotide variantNM_014685.4(HERPUD1):c.295G>A (p.Ala99Thr)not specified [RCV004221267]likely benign165693547056935470Humanname
407521770CV3437163single nucleotide variantNM_014685.4(HERPUD1):c.283C>T (p.Pro95Ser)not specified [RCV004630481]uncertain significance165693545856935458Humanname
597761033CV3685607single nucleotide variantNM_014685.4(HERPUD1):c.283C>G (p.Pro95Ala)not specified [RCV004925821]uncertain significance165693545856935458Humanname
597761038CV3685608single nucleotide variantNM_014685.4(HERPUD1):c.292A>G (p.Asn98Asp)not specified [RCV004925822]uncertain significance165693546756935467Humanname
401738595CV2676329single nucleotide variantNM_014685.4(HERPUD1):c.980T>G (p.Val327Gly)not specified [RCV004286363]uncertain significance165694220656942206Humanname
405803195CV3273820single nucleotide variantNM_014685.4(HERPUD1):c.316G>A (p.Glu106Lys)not specified [RCV004404316]uncertain significance165693670256936702Humanname
405803197CV3273821single nucleotide variantNM_014685.4(HERPUD1):c.477C>G (p.Phe159Leu)not specified [RCV004404317]uncertain significance165693928256939282Humanname
405803199CV3273822single nucleotide variantNM_014685.4(HERPUD1):c.912C>A (p.His304Gln)not specified [RCV004404318]uncertain significance165694213856942138Humanname
405803203CV3273824single nucleotide variantNM_014685.4(HERPUD1):c.941C>T (p.Pro314Leu)not specified [RCV004404320]likely benign165694216756942167Humanname
407521764CV3437161single nucleotide variantNM_014685.4(HERPUD1):c.485A>G (p.Tyr162Cys)not specified [RCV004630479]uncertain significance165693929056939290Humanname
407521767CV3437162single nucleotide variantNM_014685.4(HERPUD1):c.668A>C (p.Asn223Thr)not specified [RCV004630480]uncertain significance165694000856940008Humanname
407521773CV3437164single nucleotide variantNM_014685.4(HERPUD1):c.553T>C (p.Tyr185His)not specified [RCV004630482]uncertain significance165693935856939358Humanname
597761022CV3685605single nucleotide variantNM_014685.4(HERPUD1):c.935C>T (p.Pro312Leu)not specified [RCV004925819]uncertain significance165694216156942161Humanname
597761027CV3685606single nucleotide variantNM_014685.4(HERPUD1):c.847T>C (p.Phe283Leu)not specified [RCV004925820]uncertain significance165694018756940187Humanname
597761043CV3685609single nucleotide variantNM_014685.4(HERPUD1):c.565A>G (p.Thr189Ala)not specified [RCV004925823]uncertain significance165693990556939905Humanname
597761059CV3685613single nucleotide variantNM_014685.4(HERPUD1):c.838A>G (p.Ile280Val)not specified [RCV004925826]uncertain significance165694017856940178Humanname
597761070CV3685615single nucleotide variantNM_014685.4(HERPUD1):c.964G>A (p.Gly322Ser)not specified [RCV004925828]uncertain significance165694219056942190Humanname
598275118CV3978637single nucleotide variantNM_014685.4(HERPUD1):c.913G>A (p.Val305Ile)not specified [RCV005351763]uncertain significance165694213956942139Humanname
598275120CV3978638single nucleotide variantNM_014685.4(HERPUD1):c.586G>C (p.Val196Leu)not specified [RCV005351764]uncertain significance165693992656939926Humanname
598275122CV3978640single nucleotide variantNM_014685.4(HERPUD1):c.760G>C (p.Val254Leu)not specified [RCV005351765]uncertain significance165694010056940100Humanname
597761049CV3685610single nucleotide variantNM_014685.4(HERPUD1):c.1171A>C (p.Asn391His)not specified [RCV004925824]uncertain significance165694328556943285Humanname
598247685CV3978639single nucleotide variantNM_014685.4(HERPUD1):c.1098T>A (p.Phe366Leu)not specified [RCV005345337]uncertain significance165694321256943212Humanname
598275124CV3978641single nucleotide variantNM_014685.4(HERPUD1):c.1043A>G (p.Asn348Ser)not specified [RCV005351766]uncertain significance165694315756943157Humanname
598275127CV3978642single nucleotide variantNM_014685.4(HERPUD1):c.1045C>A (p.His349Asn)not specified [RCV005351767]uncertain significance165694315956943159Humanname
126908685CV969958deletionNM_014685.4(HERPUD1):c.584_585del (p.Phe195fs)Hereditary breast ovarian cancer syndrome [RCV001374513]pathogenic165693992256939923Human1name