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_000297.4(PKD2):c.2020-1_2020delPKD2Pathogenic/Likely pathogenic48898305688983057CAGCcriteria provided, multiple submitters, no conflictsClinGen:CA658657395
single nucleotide variantNM_000297.4(PKD2):c.2019+1G>APKD2Pathogenic/Likely pathogenic48897925688979256GAcriteria provided, multiple submitters, no conflictsClinGen:CA357623301
single nucleotide variantNM_000297.4(PKD2):c.1906C>A (p.Gln636Lys)PKD2Likely pathogenic48897914288979142CAcriteria provided, single submitterClinGen:CA220615
single nucleotide variantNM_000297.4(PKD2):c.1898+5G>APKD2Pathogenic/Likely pathogenic48897742488977424GAcriteria provided, multiple submitters, no conflictsClinGen:CA658657394
single nucleotide variantNM_000297.4(PKD2):c.1774C>T (p.Arg592Ter)PKD2Pathogenic48897729588977295CTcriteria provided, multiple submitters, no conflictsClinGen:CA357622723
DeletionNM_000297.4(PKD2):c.1671_1678del (p.Phe558fs)PKD2Pathogenic48897326288973269TACAGTTCATcriteria provided, multiple submitters, no conflictsClinGen:CA658657393
DuplicationNM_000297.4(PKD2):c.1668dup (p.Gln557fs)PKD2Pathogenic/Likely pathogenic48897326188973262TTAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_000297.4(PKD2):c.1548+1G>APKD2Pathogenic/Likely pathogenic48896802388968023GAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_000297.4(PKD2):c.1390C>T (p.Arg464Ter)PKD2Pathogenic48896786488967864CTcriteria provided, multiple submitters, no conflictsClinGen:CA123164,OMIM:173910.0005
single nucleotide variantNM_000297.4(PKD2):c.1325T>A (p.Leu442Ter)PKD2Pathogenic48896779988967799TAcriteria provided, single submitter-