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Variants search result for Homo sapiens
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39 records found for search term Yod1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405802810CV3360013single nucleotide variantNM_018566.4(YOD1):c.81C>T (p.Ala27=)not specified [RCV004478491]likely benign1207050950207050950Humanname
597805064CV3627356single nucleotide variantNM_018566.4(YOD1):c.11C>T (p.Pro4Leu)not specified [RCV004882594]uncertain significance1207051020207051020Humanname
155900835CV2241839single nucleotide variantNM_018566.4(YOD1):c.74A>G (p.Gln25Arg)not specified [RCV004106766]uncertain significance1207050957207050957Humanname
156054679CV2243116single nucleotide variantNM_018566.4(YOD1):c.56C>T (p.Pro19Leu)not specified [RCV004110025]uncertain significance1207050975207050975Humanname
156193286CV2301958single nucleotide variantNM_018566.4(YOD1):c.58G>C (p.Gly20Arg)not specified [RCV004156732]uncertain significance1207050973207050973Humanname
156191707CV2335908single nucleotide variantNM_018566.4(YOD1):c.37C>T (p.His13Tyr)not specified [RCV004196548]uncertain significance1207050994207050994Humanname
155998742CV2373330single nucleotide variantNM_018566.4(YOD1):c.70C>A (p.Gln24Lys)not specified [RCV004220040]uncertain significance1207050961207050961Humanname
329386110CV2428198single nucleotide variantNM_018566.4(YOD1):c.55C>T (p.Pro19Ser)not specified [RCV004251235]uncertain significance1207050976207050976Humanname
405802806CV3360011single nucleotide variantNM_018566.4(YOD1):c.43G>T (p.Ala15Ser)not specified [RCV004478489]uncertain significance1207050988207050988Humanname
405802812CV3360014single nucleotide variantNM_018566.4(YOD1):c.88A>G (p.Lys30Glu)not specified [RCV004478492]uncertain significance1207050943207050943Humanname
405802814CV3360015single nucleotide variantNM_018566.4(YOD1):c.91G>A (p.Ala31Thr)not specified [RCV004478493]uncertain significance1207050940207050940Humanname
597752254CV3627354single nucleotide variantNM_018566.4(YOD1):c.79G>C (p.Ala27Pro)not specified [RCV004892908]uncertain significance1207050952207050952Humanname
598242430CV3934018single nucleotide variantNM_018566.4(YOD1):c.92C>G (p.Ala31Gly)not specified [RCV005297109]uncertain significance1207050939207050939Humanname
156173670CV2194369single nucleotide variantNM_018566.4(YOD1):c.124C>T (p.Arg42Trp)not specified [RCV004079475]uncertain significance1207050907207050907Humanname
155956814CV2281971single nucleotide variantNM_018566.4(YOD1):c.290G>A (p.Cys97Tyr)not specified [RCV004138736]uncertain significance1207050741207050741Humanname
156043020CV2342282single nucleotide variantNM_018566.4(YOD1):c.253G>T (p.Gly85Cys)not specified [RCV004191853]uncertain significance1207050778207050778Humanname
407456609CV3493855single nucleotide variantNM_018566.4(YOD1):c.185G>A (p.Gly62Glu)not specified [RCV004685983]uncertain significance1207050846207050846Humanname
597805070CV3627359single nucleotide variantNM_018566.4(YOD1):c.112C>A (p.Pro38Thr)not specified [RCV004882597]uncertain significance1207050919207050919Humanname
598242408CV3934012single nucleotide variantNM_018566.4(YOD1):c.179T>C (p.Leu60Ser)not specified [RCV005297105]uncertain significance1207050852207050852Humanname
598196063CV3934014single nucleotide variantNM_018566.4(YOD1):c.115G>A (p.Val39Met)not specified [RCV005313449]uncertain significance1207050916207050916Humanname
156186377CV2232650single nucleotide variantNM_018566.4(YOD1):c.539C>G (p.Pro180Arg)not specified [RCV004101322]uncertain significance1207049528207049528Humanname
156087869CV2241359single nucleotide variantNM_018566.4(YOD1):c.453A>T (p.Arg151Ser)not specified [RCV004102493]uncertain significance1207049614207049614Humanname
156054202CV2269564single nucleotide variantNM_018566.4(YOD1):c.640A>G (p.Lys214Glu)not specified [RCV004124666]uncertain significance1207049427207049427Humanname
156059681CV2317001single nucleotide variantNM_018566.4(YOD1):c.549A>C (p.Arg183Ser)not specified [RCV004174498]uncertain significance1207049518207049518Humanname
156334694CV2333420single nucleotide variantNM_018566.4(YOD1):c.598G>A (p.Ala200Thr)not specified [RCV004190126]uncertain significance1207049469207049469Humanname
329382067CV2438411single nucleotide variantNM_018566.4(YOD1):c.614C>A (p.Thr205Lys)not specified [RCV004259568]uncertain significance1207049453207049453Humanname
329392044CV2470322single nucleotide variantNM_018566.4(YOD1):c.761G>C (p.Gly254Ala)not specified [RCV004279716]uncertain significance1207049306207049306Humanname
401887810CV2770463single nucleotide variantNM_018566.4(YOD1):c.590A>G (p.Tyr197Cys)not specified [RCV004358100]uncertain significance1207049477207049477Humanname
405802808CV3360012single nucleotide variantNM_018566.4(YOD1):c.541G>A (p.Glu181Lys)not specified [RCV004478490]uncertain significance1207049526207049526Humanname
407465768CV3493853single nucleotide variantNM_018566.4(YOD1):c.424G>C (p.Val142Leu)not specified [RCV004688858]uncertain significance1207049643207049643Humanname
597805062CV3627355single nucleotide variantNM_018566.4(YOD1):c.601A>G (p.Ile201Val)not specified [RCV004882593]uncertain significance1207049466207049466Humanname
597805065CV3627357single nucleotide variantNM_018566.4(YOD1):c.770A>G (p.Lys257Arg)not specified [RCV004882595]uncertain significance1207049297207049297Humanname
597805067CV3627358single nucleotide variantNM_018566.4(YOD1):c.620A>T (p.Gln207Leu)not specified [RCV004882596]uncertain significance1207049447207049447Humanname
598242414CV3934013single nucleotide variantNM_018566.4(YOD1):c.500A>G (p.Tyr167Cys)not specified [RCV005297106]uncertain significance1207049567207049567Humanname
598196069CV3934015single nucleotide variantNM_018566.4(YOD1):c.944G>T (p.Arg315Leu)not specified [RCV005313450]uncertain significance1207049123207049123Humanname
598242420CV3934016single nucleotide variantNM_018566.4(YOD1):c.856T>G (p.Phe286Val)not specified [RCV005297107]uncertain significance1207049211207049211Humanname
598242425CV3934017single nucleotide variantNM_018566.4(YOD1):c.994G>A (p.Glu332Lys)not specified [RCV005297108]uncertain significance1207049073207049073Humanname
598242435CV3934019single nucleotide variantNM_018566.4(YOD1):c.434C>T (p.Thr145Ile)not specified [RCV005297110]uncertain significance1207049633207049633Humanname
329362466CV2444735single nucleotide variantNM_018566.4(YOD1):c.1031A>G (p.Asn344Ser)not specified [RCV004258987]uncertain significance1207049036207049036Humanname