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)
DeletionNM_001009944.3(PKD1):c.6583_6589del (p.Cys2195fs)PKD1Pathogenic1621585792158585CGCTGGCACcriteria provided, multiple submitters, no conflictsClinGen:CA645509211
single nucleotide variantNM_001009944.3(PKD1):c.4258G>T (p.Glu1420Ter)PKD1Pathogenic1621609102160910CAcriteria provided, single submitterClinGen:CA394380975
single nucleotide variantNM_001009944.3(PKD1):c.3285C>A (p.Tyr1095Ter)PKD1Pathogenic1621623512162351GTcriteria provided, single submitterClinGen:CA394383399
single nucleotide variantNM_001009944.3(PKD1):c.2932C>T (p.Gln978Ter)PKD1Pathogenic1621632152163215GAcriteria provided, multiple submitters, no conflictsClinGen:CA394385563
single nucleotide variantNM_001009944.3(PKD1):c.2152C>T (p.Gln718Ter)PKD1Pathogenic1621648722164872GAcriteria provided, multiple submitters, no conflictsClinGen:CA394389261
single nucleotide variantNM_001009944.3(PKD1):c.8704C>T (p.Gln2902Ter)PKD1Pathogenic1621533542153354GAcriteria provided, multiple submitters, no conflictsClinGen:CA394362329
DeletionNM_001009944.3(PKD1):c.12230_12239del (p.Ala4077fs)PKD1Likely pathogenic1621404912140500CCAGGACTCGGCcriteria provided, single submitterClinGen:CA658653829
DeletionNM_000297.4(PKD2):c.514del (p.Asp172fs)PKD2Pathogenic48892939688929396CGCcriteria provided, multiple submitters, no conflictsClinGen:CA658657391
single nucleotide variantNM_000297.4(PKD2):c.603G>A (p.Trp201Ter)PKD2Pathogenic48894061788940617GAcriteria provided, single submitterClinGen:CA357628188
single nucleotide variantNM_000297.4(PKD2):c.964C>T (p.Arg322Trp)PKD2Pathogenic/Likely pathogenic48895952388959523CTcriteria provided, multiple submitters, no conflictsClinGen:CA357632796