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42 records found for search term Abhd11
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
617153178CV4021152single nucleotide variantNM_148912.4(ABHD11):c.225C>T (p.Ser75=)not provided [RCV005428905]likely benign77373836473738364Humanname
156272632CV2277554single nucleotide variantNM_148912.4(ABHD11):c.50C>G (p.Pro17Arg)not specified [RCV004145241]uncertain significance77373872173738721Humanname
405675559CV3286750single nucleotide variantNM_148912.4(ABHD11):c.76C>T (p.Pro26Ser)not specified [RCV004420558]uncertain significance77373869573738695Humanname
598159483CV3901061single nucleotide variantNM_148912.4(ABHD11):c.73G>T (p.Val25Leu)not specified [RCV005260743]uncertain significance77373869873738698Humanname
155957987CV2282139single nucleotide variantNM_148912.4(ABHD11):c.158G>T (p.Gly53Val)not specified [RCV004138873]uncertain significance77373843173738431Humanname
156124209CV2285741single nucleotide variantNM_148912.4(ABHD11):c.146G>A (p.Arg49Lys)not specified [RCV004141884]likely benign77373844373738443Humanname
156003106CV2288230single nucleotide variantNM_148912.4(ABHD11):c.269C>G (p.Thr90Arg)not specified [RCV004149741]uncertain significance77373772873737728Humanname
401727948CV2675876single nucleotide variantNM_148912.4(ABHD11):c.286C>G (p.His96Asp)not specified [RCV004281880]uncertain significance77373771173737711Humanname
401898040CV2780092single nucleotide variantNM_148912.4(ABHD11):c.201C>A (p.Phe67Leu)not specified [RCV004355753]uncertain significance77373838873738388Humanname
405675609CV3286760single nucleotide variantNM_148912.4(ABHD11):c.214A>G (p.Asn72Asp)not specified [RCV004420568]uncertain significance77373837573738375Humanname
405675613CV3286761single nucleotide variantNM_148912.4(ABHD11):c.242C>T (p.Ala81Val)not specified [RCV004420569]uncertain significance77373834773738347Humanname
156319926CV2197180single nucleotide variantNM_148912.4(ABHD11):c.616G>A (p.Val206Met)not specified [RCV004078970]uncertain significance77373710173737101Humanname
156201811CV2234418single nucleotide variantNM_148912.4(ABHD11):c.815G>A (p.Arg272Gln)not specified [RCV004100632]uncertain significance77373666573736665Humanname
156051623CV2238051single nucleotide variantNM_148912.4(ABHD11):c.635C>T (p.Thr212Ile)not specified [RCV004111078]uncertain significance77373708273737082Humanname
156273166CV2247580single nucleotide variantNM_148912.4(ABHD11):c.563G>T (p.Arg188Leu)not specified [RCV004108881]uncertain significance77373726473737264Humanname
156149350CV2265347single nucleotide variantNM_148912.4(ABHD11):c.457A>G (p.Ile153Val)not specified [RCV004128237]uncertain significance77373737073737370Humanname
156003321CV2293453single nucleotide variantNM_148912.4(ABHD11):c.385G>A (p.Val129Ile)not specified [RCV004152697]likely benign77373761273737612Humanname
155908182CV2302370single nucleotide variantNM_148912.4(ABHD11):c.432G>C (p.Gln144His)not specified [RCV004161122]uncertain significance77373756573737565Humanname
156000835CV2391809single nucleotide variantNM_148912.4(ABHD11):c.451C>T (p.Arg151Cys)not specified [RCV004235689]uncertain significance77373737673737376Humanname
329380723CV2440429single nucleotide variantNM_148912.4(ABHD11):c.401G>A (p.Gly134Glu)not specified [RCV004256364]uncertain significance77373759673737596Humanname
329377256CV2462476single nucleotide variantNM_148912.4(ABHD11):c.620G>A (p.Arg207Gln)not specified [RCV004276657]uncertain significance77373709773737097Humanname
401719184CV2679445single nucleotide variantNM_148912.4(ABHD11):c.563G>A (p.Arg188His)not specified [RCV004285969]likely benign77373726473737264Humanname
401737413CV2695796single nucleotide variantNM_148912.4(ABHD11):c.902T>C (p.Ile301Thr)not specified [RCV004308085]uncertain significance77373657873736578Humanname
401876327CV2770518single nucleotide variantNM_148912.4(ABHD11):c.647A>G (p.Glu216Gly)not specified [RCV004347804]uncertain significance77373707073737070Humanname
401894715CV2785220single nucleotide variantNM_148912.4(ABHD11):c.427C>G (p.Leu143Val)not specified [RCV004356995]uncertain significance77373757073737570Humanname
405675637CV3286765single nucleotide variantNM_148912.4(ABHD11):c.356C>T (p.Pro119Leu)not specified [RCV004420573]uncertain significance77373764173737641Humanname
405675664CV3286771single nucleotide variantNM_148912.4(ABHD11):c.379G>A (p.Val127Ile)not specified [RCV004420579]uncertain significance77373761873737618Humanname
405676339CV3286803single nucleotide variantNM_148912.4(ABHD11):c.619C>T (p.Arg207Trp)not specified [RCV004420611]uncertain significance77373709873737098Humanname
405675791CV3286821single nucleotide variantNM_148912.4(ABHD11):c.842C>T (p.Thr281Met)not specified [RCV004420629]uncertain significance77373663873736638Humanname
407476512CV3476511single nucleotide variantNM_148912.4(ABHD11):c.878G>A (p.Arg293His)not specified [RCV004663494]uncertain significance77373660273736602Humanname
407476847CV3476616single nucleotide variantNM_148912.4(ABHD11):c.894A>G (p.Ile298Met)not specified [RCV004663577]likely benign77373658673736586Humanname
407477136CV3476721single nucleotide variantNM_148912.4(ABHD11):c.648G>C (p.Glu216Asp)not specified [RCV004663647]uncertain significance77373706973737069Humanname
407477376CV3476822single nucleotide variantNM_148912.4(ABHD11):c.791C>G (p.Pro264Arg)not specified [RCV004663719]uncertain significance77373668973736689Humanname
597745019CV3587364single nucleotide variantNM_148912.4(ABHD11):c.541G>A (p.Ala181Thr)not specified [RCV004845367]uncertain significance77373728673737286Humanname
597745462CV3587422single nucleotide variantNM_148912.4(ABHD11):c.504T>A (p.Phe168Leu)not specified [RCV004845425]uncertain significance77373732373737323Humanname
597745675CV3587461single nucleotide variantNM_148912.4(ABHD11):c.824C>A (p.Pro275His)not specified [RCV004845464]uncertain significance77373665673736656Humanname
598160190CV3897362single nucleotide variantNM_148912.4(ABHD11):c.374C>T (p.Pro125Leu)not specified [RCV005260930]uncertain significance77373762373737623Humanname
598168759CV3897462single nucleotide variantNM_148912.4(ABHD11):c.677A>G (p.Asn226Ser)not specified [RCV005262674]uncertain significance77373704073737040Humanname
598158988CV3900921single nucleotide variantNM_148912.4(ABHD11):c.827G>C (p.Arg276Pro)not specified [RCV005260608]uncertain significance77373665373736653Humanname
598159169CV3900967single nucleotide variantNM_148912.4(ABHD11):c.355C>T (p.Pro119Ser)not specified [RCV005260654]uncertain significance77373764273737642Humanname
598159819CV3901153single nucleotide variantNM_148912.4(ABHD11):c.352C>G (p.Leu118Val)not specified [RCV005260834]uncertain significance77373764573737645Humanname
38463997CV961286single nucleotide variantNM_148912.4(ABHD11):c.397A>G (p.Met133Val)not provided [RCV001249410]not provided77373760073737600Humanname