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Variants search result for Homo sapiens
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22 records found for search term Id1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329394478CV2469892single nucleotide variantNM_002165.4(ID1):c.15T>G (p.Ser5Arg)not specified [RCV004285362]uncertain significance203160540231605402Humanname
598226473CV3894385single nucleotide variantNM_002165.4(ID1):c.210C>T (p.Asn70=)not provided [RCV005257628]likely benign203160559731605597Humanname
405782250CV3267256single nucleotide variantNM_002165.4(ID1):c.41G>A (p.Gly14Asp)not specified [RCV004397822]uncertain significance203160542831605428Humanname
405782272CV3267260single nucleotide variantNM_002165.4(ID1):c.61G>C (p.Ala21Pro)not specified [RCV004397826]uncertain significance203160544831605448Humanname
405782277CV3267261single nucleotide variantNM_002165.4(ID1):c.80G>T (p.Gly27Val)not specified [RCV004397827]uncertain significance203160546731605467Humanname
155984543CV2241132single nucleotide variantNM_002165.4(ID1):c.173A>G (p.Asp58Gly)not specified [RCV004104163]uncertain significance203160556031605560Humanname
156072712CV2251505single nucleotide variantNM_002165.4(ID1):c.262A>C (p.Lys88Gln)not specified [RCV004117475]uncertain significance203160564931605649Humanname
155990253CV2372023single nucleotide variantNM_002165.4(ID1):c.146C>G (p.Ala49Gly)not specified [RCV004221696]uncertain significance203160553331605533Humanname
329391818CV2453151single nucleotide variantNM_002165.4(ID1):c.217T>C (p.Tyr73His)not specified [RCV004279532]uncertain significance203160560431605604Humanname
405782229CV3267252single nucleotide variantNM_002165.4(ID1):c.104T>A (p.Leu35Gln)not specified [RCV004397818]uncertain significance203160549131605491Humanname
407465925CV3444391single nucleotide variantNM_002165.4(ID1):c.107C>A (p.Ser36Tyr)not specified [RCV004635477]uncertain significance203160549431605494Humanname
597784202CV3683009single nucleotide variantNM_002165.4(ID1):c.111G>C (p.Glu37Asp)not specified [RCV004931616]uncertain significance203160549831605498Humanname
156374192CV2198289single nucleotide variantNM_002165.4(ID1):c.343G>C (p.Val115Leu)not specified [RCV004081844]uncertain significance203160573031605730Humanname
156158901CV2262526single nucleotide variantNM_002165.4(ID1):c.367C>G (p.Leu123Val)not specified [RCV004130742]uncertain significance203160575431605754Humanname
405782234CV3267253single nucleotide variantNM_002165.4(ID1):c.302A>G (p.Tyr101Cys)not specified [RCV004397819]uncertain significance203160568931605689Humanname
405782240CV3267254single nucleotide variantNM_002165.4(ID1):c.359G>T (p.Gly120Val)not specified [RCV004397820]uncertain significance203160574631605746Humanname
405782244CV3267255single nucleotide variantNM_002165.4(ID1):c.419C>A (p.Thr140Lys)not specified [RCV004397821]uncertain significance203160580631605806Humanname
405782255CV3267257single nucleotide variantNM_002165.4(ID1):c.445G>A (p.Asp149Asn)not specified [RCV004397823]uncertain significance203160607131606071Humanname
405782261CV3267258single nucleotide variantNM_002165.4(ID1):c.460T>C (p.Cys154Arg)not specified [RCV004397824]uncertain significance203160608631606086Humanname
407510982CV3444392single nucleotide variantNM_002165.4(ID1):c.358G>A (p.Gly120Ser)not specified [RCV004626314]uncertain significance203160574531605745Humanname
597784198CV3683007single nucleotide variantNM_002165.4(ID1):c.335A>C (p.Glu112Ala)not specified [RCV004931615]uncertain significance203160572231605722Humanname
598257585CV3979038single nucleotide variantNM_002165.4(ID1):c.463C>G (p.Arg155Gly)not specified [RCV005347023]uncertain significance203160608931606089Humanname