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.3097+2T>CPKHD1Likely pathogenic65190765551907655AGcriteria provided, single submitter-
single nucleotide variantNM_138694.4(PKHD1):c.2140+1G>TPKHD1Likely pathogenic65191787351917873CAcriteria provided, single submitter-
single nucleotide variantNM_138694.4(PKHD1):c.1397G>A (p.Gly466Glu)PKHD1Pathogenic/Likely pathogenic65192323651923236CTcriteria provided, multiple submitters, no conflicts-
DuplicationNM_138694.4(PKHD1):c.1068dup (p.Asn357Ter)PKHD1Pathogenic65192736651927367TTAcriteria provided, single submitter-
single nucleotide variantNM_138694.4(PKHD1):c.708-2A>CPKHD1Likely pathogenic65193432751934327TGcriteria provided, single submitter-
single nucleotide variantNM_138694.4(PKHD1):c.707+2T>CPKHD1Likely pathogenic65193520251935202AGcriteria provided, single submitter-
single nucleotide variantNM_138694.4(PKHD1):c.1095G>A (p.Trp365Ter)PKHD1Likely pathogenic65192734051927340CTcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_138694.4(PKHD1):c.708-1G>APKHD1Likely pathogenic65193432651934326CTcriteria provided, single submitter-
single nucleotide variantNM_138694.4(PKHD1):c.53-1G>APKHD1Likely pathogenic65194805451948054CTcriteria provided, multiple submitters, no conflicts-
InsertionNM_138694.4(PKHD1):c.5895_5896insAC (p.Leu1966fs)PKHD1Likely pathogenic65182468051824681GGGTcriteria provided, single submitter-