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.8762A>G (p.His2921Arg)PKD1Likely pathogenic1621532962153296TCcriteria provided, single submitterClinGen:CA394362115
single nucleotide variantNM_001009944.3(PKD1):c.7861G>T (p.Glu2621Ter)PKD1Pathogenic1621558682155868CAcriteria provided, single submitterClinGen:CA394367599
DeletionNM_001009944.3(PKD1):c.896_897del (p.Pro299fs)PKD1Pathogenic1621680962168097CAGCcriteria provided, single submitterClinGen:CA658798518
DeletionNM_000297.4(PKD2):c.2284_2287del (p.Tyr762fs)PKD2Pathogenic48898695688986959AGTACAcriteria provided, single submitterClinGen:CA658796448
single nucleotide variantNM_001009944.3(PKD1):c.12035G>A (p.Trp4012Ter)PKD1Pathogenic1621407782140778CTcriteria provided, multiple submitters, no conflictsClinGen:CA7828865
single nucleotide variantNM_001009944.3(PKD1):c.6877C>T (p.Pro2293Ser)PKD1Likely pathogenic1621582912158291GAcriteria provided, single submitterClinGen:CA394372711
single nucleotide variantNM_000297.4(PKD2):c.2533C>T (p.Arg845Ter)PKD2Pathogenic48899597488995974CTcriteria provided, multiple submitters, no conflictsClinGen:CA3004284
single nucleotide variantNM_001009944.3(PKD1):c.6031C>T (p.Gln2011Ter)PKD1Pathogenic1621591372159137GAcriteria provided, multiple submitters, no conflictsClinGen:CA394374645
single nucleotide variantNM_000297.4(PKD2):c.637C>T (p.Arg213Ter)PKD2Pathogenic48894065188940651CTcriteria provided, multiple submitters, no conflictsClinGen:CA10575461
IndelNM_138694.4(PKHD1):c.4352_4356delinsAAGGGGTCA (p.Pro1451fs)PKHD1Pathogenic65189025251890256CAAGGTGACCCCTTcriteria provided, single submitterClinGen:CA658796770