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Variants search result for Homo sapiens
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35 records found for search term Adrm1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597802377CV3655736single nucleotide variantNM_007002.4(ADRM1):c.25C>A (p.Pro9Thr)not specified [RCV004906546]uncertain significance206230359362303593Humanname
156338451CV2271274single nucleotide variantNM_007002.4(ADRM1):c.97C>A (p.Leu33Met)not specified [RCV004136404]uncertain significance206230366562303665Humanname
597802367CV3655743single nucleotide variantNM_007002.4(ADRM1):c.95C>A (p.Ser32Tyr)not specified [RCV004906551]uncertain significance206230366362303663Humanname
15202907CV705586single nucleotide variantNM_007002.4(ADRM1):c.735G>A (p.Ala245=)not provided [RCV000958102]benign206230770762307707Humanname
15202909CV705587single nucleotide variantNM_007002.4(ADRM1):c.798C>T (p.Asp266=)not provided [RCV000958103]benign206230777062307770Humanname
15159591CV717094single nucleotide variantNM_007002.4(ADRM1):c.945A>G (p.Pro315=)not provided [RCV000969739]benign206230810962308109Humanname
405773111CV3252610single nucleotide variantNM_007002.4(ADRM1):c.204C>A (p.Asn68Lys)not specified [RCV004385494]uncertain significance206230377262303772Humanname
598224023CV3956572single nucleotide variantNM_007002.4(ADRM1):c.116C>G (p.Thr39Ser)not specified [RCV005318162]uncertain significance206230368462303684Humanname
15121433CV742495single nucleotide variantNM_007002.4(ADRM1):c.159C>G (p.Asp53Glu)not provided [RCV000896064]benign206230372762303727Humanname
9686970CV171661single nucleotide variantNM_007002.4(ADRM1):c.653C>A (p.Pro218Gln)Prostate cancer [RCV000149189]pathogenic|uncertain significance206230762562307625Human2name
156157585CV2322582single nucleotide variantNM_007002.4(ADRM1):c.376G>A (p.Glu126Lys)not specified [RCV004182733]uncertain significance206230624262306242Humanname
329394197CV2472375single nucleotide variantNM_007002.4(ADRM1):c.580T>A (p.Leu194Ile)not specified [RCV004285253]uncertain significance206230740962307409Humanname
401743668CV2684756single nucleotide variantNM_007002.4(ADRM1):c.526G>A (p.Gly176Ser)not specified [RCV004293840]uncertain significance206230671962306719Humanname
401740293CV2705960single nucleotide variantNM_007002.4(ADRM1):c.881C>T (p.Pro294Leu)not specified [RCV004320882]uncertain significance206230804562308045Humanname
401752088CV2714056single nucleotide variantNM_007002.4(ADRM1):c.668C>T (p.Ser223Phe)not specified [RCV004315457]uncertain significance206230764062307640Humanname
401768309CV2720064single nucleotide variantNM_007002.4(ADRM1):c.818C>T (p.Thr273Met)not specified [RCV004323637]uncertain significance206230779062307790Humanname
401878657CV2776890single nucleotide variantNM_007002.4(ADRM1):c.674C>T (p.Thr225Ile)not specified [RCV004351714]uncertain significance206230764662307646Humanname
405773275CV3252615single nucleotide variantNM_007002.4(ADRM1):c.358C>T (p.His120Tyr)not specified [RCV004385499]uncertain significance206230622462306224Humanname
405773397CV3252636single nucleotide variantNM_007002.4(ADRM1):c.839C>T (p.Pro280Leu)not specified [RCV004385520]uncertain significance206230781162307811Humanname
405773426CV3252642single nucleotide variantNM_007002.4(ADRM1):c.970G>A (p.Ala324Thr)not specified [RCV004385526]uncertain significance206230813462308134Humanname
407490012CV3431016single nucleotide variantNM_007002.4(ADRM1):c.676C>T (p.Arg226Cys)not specified [RCV004620060]uncertain significance206230764862307648Humanname
407490050CV3431025single nucleotide variantNM_007002.4(ADRM1):c.730C>T (p.Pro244Ser)not specified [RCV004620069]uncertain significance206230770262307702Humanname
597802137CV3655725single nucleotide variantNM_007002.4(ADRM1):c.962C>T (p.Pro321Leu)not specified [RCV004906536]uncertain significance206230812662308126Humanname
597802077CV3659192single nucleotide variantNM_007002.4(ADRM1):c.809T>G (p.Ile270Ser)not specified [RCV004906504]uncertain significance206230778162307781Humanname
597802097CV3659203single nucleotide variantNM_007002.4(ADRM1):c.715G>A (p.Ala239Thr)not specified [RCV004906515]uncertain significance206230768762307687Humanname
597802116CV3659213single nucleotide variantNM_007002.4(ADRM1):c.925C>T (p.Arg309Cys)not specified [RCV004906525]uncertain significance206230808962308089Humanname
598223890CV3956552single nucleotide variantNM_007002.4(ADRM1):c.446C>G (p.Ala149Gly)not specified [RCV005318142]uncertain significance206230631262306312Humanname
15175878CV717095single nucleotide variantNM_007002.4(ADRM1):c.971C>T (p.Ala324Val)not provided [RCV000973054]benign206230813562308135Humanname
156032210CV2218258single nucleotide variantNM_007002.4(ADRM1):c.1199A>G (p.Glu400Gly)not specified [RCV004088453]uncertain significance206230873662308736Humanname
155995413CV2259057single nucleotide variantNM_007002.4(ADRM1):c.1174G>A (p.Gly392Ser)not specified [RCV004120321]uncertain significance206230871162308711Humanname
156003849CV2295773single nucleotide variantNM_007002.4(ADRM1):c.1210A>G (p.Met404Val)not specified [RCV004151701]uncertain significance206230874762308747Humanname
597712218CV3655749single nucleotide variantNM_007002.4(ADRM1):c.1025T>C (p.Met342Thr)not specified [RCV004917915]uncertain significance206230837862308378Humanname
597802062CV3659184single nucleotide variantNM_007002.4(ADRM1):c.1144C>G (p.Gln382Glu)not specified [RCV004906496]uncertain significance206230868162308681Humanname
598223823CV3956542single nucleotide variantNM_007002.4(ADRM1):c.1181C>T (p.Thr394Met)not specified [RCV005318132]uncertain significance206230871862308718Humanname
598223956CV3956562single nucleotide variantNM_007002.4(ADRM1):c.1136A>G (p.Lys379Arg)not specified [RCV005318152]uncertain significance206230867362308673Humanname