Knowledge base for genomic medicine in Japanese
多発性嚢胞腎
Excelでダウンロード
表のタイトル行が青色の項目は、クリックすることでソートすることができます。
TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DeletionNM_000297.4(PKD2):c.2524del (p.Leu842fs)PKD2Pathogenic48899596488995964GCGcriteria provided, single submitterClinGen:CA645509148
DeletionNM_000297.4(PKD2):c.481_502del (p.Gly161fs)PKD2Pathogenic48892936288929383ACCAGGGCCCGCCGTGCCCCAGCAcriteria provided, single submitterClinGen:CA645509147
DeletionNM_000297.4(PKD2):c.2159del (p.Asn720fs)PKD2Pathogenic48898655988986559GAGcriteria provided, multiple submitters, no conflictsClinGen:CA3004147
single nucleotide variantNM_000297.4(PKD2):c.2523-1G>APKD2Pathogenic48899596388995963GAcriteria provided, single submitterClinGen:CA357627494
DeletionNM_001009944.3(PKD1):c.11912del (p.Pro3971fs)PKD1Pathogenic1621409762140976CGCcriteria provided, single submitterClinGen:CA645509208
single nucleotide variantNM_001009944.3(PKD1):c.11713-1G>APKD1Pathogenic/Likely pathogenic1621411762141176CTcriteria provided, multiple submitters, no conflictsClinGen:CA394330362
DeletionNM_001009944.3(PKD1):c.11538-2delPKD1Pathogenic1621416002141600CTCcriteria provided, single submitterClinGen:CA645509210
single nucleotide variantNM_001009944.3(PKD1):c.11156G>A (p.Arg3719Gln)PKD1Pathogenic1621429552142955CTcriteria provided, multiple submitters, no conflictsClinGen:CA394336677
DeletionNM_001009944.3(PKD1):c.9994del (p.Val3332fs)PKD1Pathogenic1621497012149701ACAcriteria provided, single submitterClinGen:CA645509217
single nucleotide variantNM_001009944.3(PKD1):c.8905C>T (p.Gln2969Ter)PKD1Pathogenic1621528582152858GAcriteria provided, multiple submitters, no conflictsClinGen:CA394361576