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)
DuplicationNM_001009944.3(PKD1):c.8972dup (p.Tyr2991Ter)PKD1Pathogenic1621526102152611GGTcriteria provided, multiple submitters, no conflicts-
DeletionNM_001009944.3(PKD1):c.8333del (p.Gly2778fs)PKD1Pathogenic1621537252153725GCGcriteria provided, single submitter-
DeletionNM_001009944.3(PKD1):c.8017-2_8017-1delPKD1Pathogenic/Likely pathogenic1621546442154645CCTCcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_001009944.3(PKD1):c.7204C>T (p.Arg2402Ter)PKD1Pathogenic1621568112156811GAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_001009944.3(PKD1):c.6727C>T (p.Gln2243Ter)PKD1Pathogenic1621584412158441GAcriteria provided, multiple submitters, no conflicts-
DuplicationNM_001009944.3(PKD1):c.6587_6593dup (p.Gly2199fs)PKD1Pathogenic1621585742158575CCGGCCGCTcriteria provided, single submitter-
IndelNM_001009944.3(PKD1):c.5913delinsACC (p.Ser1972fs)PKD1Likely pathogenic1621592552159255CGGTcriteria provided, single submitter-
DuplicationNM_001009944.3(PKD1):c.4894_4901dup (p.Gly1634_Leu1635insTer)PKD1Likely pathogenic1621602662160267CCCCCTCTATcriteria provided, single submitter-
single nucleotide variantNM_001009944.3(PKD1):c.4444C>T (p.Gln1482Ter)PKD1Pathogenic1621607242160724GAcriteria provided, multiple submitters, no conflicts-
DeletionNM_001009944.3(PKD1):c.3601_3620del (p.Ala1201fs)PKD1Pathogenic1621615482161567GCGCACATCCGCCTGGGCCGCGcriteria provided, single submitter-