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_001009944.3(PKD1):c.8017-2A>GPKD1Pathogenic1621546452154645TCcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_000297.4(PKD2):c.1548+1G>APKD2Pathogenic/Likely pathogenic48896802388968023GAcriteria provided, multiple submitters, no conflicts-
DeletionNM_001009944.3(PKD1):c.11379del (p.Thr3794fs)PKD1Pathogenic1621420802142080TCTcriteria provided, multiple submitters, no conflicts-
DuplicationNM_001009944.3(PKD1):c.2494dup (p.Arg832fs)PKD1Pathogenic1621645292164530CCGcriteria provided, multiple submitters, no conflicts-
DuplicationNM_001009944.3(PKD1):c.755dup (p.Pro253fs)PKD1Pathogenic1621682372168238CCGcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_000297.4(PKD2):c.2286C>A (p.Tyr762Ter)PKD2Pathogenic48898695988986959CAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_001009944.3(PKD1):c.5878C>T (p.Gln1960Ter)PKD1Pathogenic1621592902159290GAcriteria provided, single submitter-
DuplicationNM_000297.4(PKD2):c.538dup (p.Leu180fs)PKD2Pathogenic48892941888929419TTCcriteria provided, single submitter-
DuplicationNM_001009944.3(PKD1):c.2085dup (p.Ala696fs)PKD1Pathogenic1621653902165391CCGcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_001009944.3(PKD1):c.7327G>T (p.Gly2443Ter)PKD1Pathogenic1621565612156561CAcriteria provided, multiple submitters, no conflicts-