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29 records found for search term Abhd3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597683947CV3585747single nucleotide variantNM_138340.5(ABHD3):c.18G>C (p.Met6Ile)not specified [RCV004858122]uncertain significance182170464821704648Humanname
15194339CV704548single nucleotide variantNM_138340.5(ABHD3):c.819C>T (p.Thr273=)not provided [RCV000955619]benign182165919321659193Humanname
155972890CV2335857single nucleotide variantNM_138340.5(ABHD3):c.250G>A (p.Val84Ile)not specified [RCV004196082]uncertain significance182170366021703660Humanname
156391470CV2382323single nucleotide variantNM_138340.5(ABHD3):c.191G>A (p.Ser64Asn)not specified [RCV004230670]uncertain significance182170371921703719Humanname
407511402CV3477880single nucleotide variantNM_138340.5(ABHD3):c.213C>A (p.Asp71Glu)not specified [RCV004673084]uncertain significance182170369721703697Humanname
407525755CV3478043single nucleotide variantNM_138340.5(ABHD3):c.116G>A (p.Gly39Asp)not specified [RCV004679411]uncertain significance182170455021704550Humanname
597752939CV3585613single nucleotide variantNM_138340.5(ABHD3):c.100T>A (p.Leu34Ile)not specified [RCV004846939]uncertain significance182170456621704566Humanname
597753122CV3585791single nucleotide variantNM_138340.5(ABHD3):c.251T>C (p.Val84Ala)not specified [RCV004847011]uncertain significance182170365921703659Humanname
156315078CV2196740single nucleotide variantNM_138340.5(ABHD3):c.899C>G (p.Ser300Cys)not specified [RCV004069423]uncertain significance182165701921657019Humanname
156134317CV2347013single nucleotide variantNM_138340.5(ABHD3):c.559C>A (p.Pro187Thr)not provided [RCV004695664]|not specified [RCV004204501]uncertain significance182166422721664227Humanname
155995414CV2374999single nucleotide variantNM_138340.5(ABHD3):c.698T>C (p.Ile233Thr)not specified [RCV004230054]uncertain significance182165931421659314Humanname
156084037CV2395115single nucleotide variantNM_138340.5(ABHD3):c.710C>T (p.Thr237Met)not specified [RCV004236793]uncertain significance182165930221659302Humanname
329352348CV2452900single nucleotide variantNM_138340.5(ABHD3):c.530G>A (p.Arg177Lys)not specified [RCV004277540]uncertain significance182168394521683945Humanname
401718973CV2704894single nucleotide variantNM_138340.5(ABHD3):c.697A>T (p.Ile233Phe)not specified [RCV004307469]uncertain significance182165931521659315Humanname
401752714CV2707101single nucleotide variantNM_138340.5(ABHD3):c.311C>T (p.Pro104Leu)not specified [RCV004321684]uncertain significance182170359921703599Humanname
405700883CV3279903single nucleotide variantNM_138340.5(ABHD3):c.376G>A (p.Asp126Asn)not specified [RCV004425385]uncertain significance182170244921702449Humanname
405700944CV3279913single nucleotide variantNM_138340.5(ABHD3):c.628C>T (p.Pro210Ser)not specified [RCV004425395]uncertain significance182166415821664158Humanname
405701018CV3279925single nucleotide variantNM_138340.5(ABHD3):c.739G>A (p.Val247Ile)not specified [RCV004425407]uncertain significance182165927321659273Humanname
407525709CV3477963single nucleotide variantNM_138340.5(ABHD3):c.426C>G (p.Ile142Met)not specified [RCV004679394]uncertain significance182170239921702399Humanname
597753316CV3582411single nucleotide variantNM_138340.5(ABHD3):c.461A>T (p.Glu154Val)not specified [RCV004847052]uncertain significance182170236421702364Humanname
598254802CV3898916single nucleotide variantNM_138340.5(ABHD3):c.586G>A (p.Glu196Lys)not specified [RCV005259789]uncertain significance182166420021664200Humanname
598255721CV3909030single nucleotide variantNM_138340.5(ABHD3):c.307C>T (p.Pro103Ser)not specified [RCV005259958]uncertain significance182170360321703603Humanname
598166199CV3909105single nucleotide variantNM_138340.5(ABHD3):c.487C>G (p.Leu163Val)not specified [RCV005262012]uncertain significance182170233821702338Humanname
598166311CV3909132single nucleotide variantNM_138340.5(ABHD3):c.550C>T (p.Leu184Phe)not specified [RCV005262038]uncertain significance182168392521683925Humanname
156122874CV2227178single nucleotide variantNM_138340.5(ABHD3):c.1112C>G (p.Ser371Cys)not specified [RCV004091787]uncertain significance182165170921651709Humanname
156056412CV2308905single nucleotide variantNM_138340.5(ABHD3):c.1169T>C (p.Met390Thr)not specified [RCV004169197]uncertain significance182165165221651652Humanname
155919375CV2333184single nucleotide variantNM_138340.5(ABHD3):c.1220A>T (p.Glu407Val)not specified [RCV004194473]uncertain significance182165160121651601Humanname
597684718CV3582495single nucleotide variantNM_138340.5(ABHD3):c.1124A>G (p.His375Arg)not specified [RCV004858203]uncertain significance182165169721651697Humanname
598166084CV3909077single nucleotide variantNM_138340.5(ABHD3):c.1088C>T (p.Pro363Leu)not specified [RCV005261986]uncertain significance182165173321651733Humanname