Knowledge base for genomic medicine in Japanese
多発性嚢胞腎
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
single nucleotide variantNM_138694.4(PKHD1):c.8518C>T (p.Arg2840Cys)PKHD1Pathogenic/Likely pathogenic65164064251640642GAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_138694.4(PKHD1):c.4330C>T (p.Gln1444Ter)PKHD1Pathogenic/Likely pathogenic65189027851890278GAcriteria provided, multiple submitters, no conflicts-
DeletionNM_138694.4(PKHD1):c.3958_3959del (p.Gly1320fs)PKHD1Pathogenic65189064951890650TCCTcriteria provided, single submitter-
single nucleotide variantNM_138694.4(PKHD1):c.3539G>A (p.Gly1180Glu)PKHD1Likely pathogenic65189297551892975CTcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_138694.4(PKHD1):c.3467C>T (p.Ser1156Leu)PKHD1Pathogenic/Likely pathogenic65189304751893047GAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_138694.4(PKHD1):c.7109+3A>CPKHD1Likely pathogenic65175192851751928TGcriteria provided, single submitter-
single nucleotide variantNM_138694.4(PKHD1):c.2279+5G>APKHD1Likely pathogenic65191495051914950CTcriteria provided, single submitter-
single nucleotide variantNM_138694.4(PKHD1):c.778+1G>CPKHD1Likely pathogenic65193425451934254CGcriteria provided, multiple submitters, no conflicts-
DeletionNM_138694.4(PKHD1):c.3907del (p.Val1303fs)PKHD1Pathogenic65189070151890701ACAcriteria provided, single submitter-
DeletionNM_138694.4(PKHD1):c.10126del (p.Ala3376fs)PKHD1Pathogenic65160921351609213GCGcriteria provided, multiple submitters, no conflicts-