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_138694.4(PKHD1):c.778+1G>CPKHD1Likely pathogenic65193425451934254CGcriteria provided, multiple submitters, no conflicts-
DuplicationNM_001009944.3(PKD1):c.11412-2dupPKD1Likely pathogenic1621419082141909CCTcriteria provided, single submitter-
DeletionNM_001009944.3(PKD1):c.10821+1delPKD1Likely pathogenic1621438112143811ACAcriteria provided, single submitter-
single nucleotide variantNM_001009944.3(PKD1):c.8016+2T>CPKD1Likely pathogenic1621553212155321AGcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_001009944.3(PKD1):c.1202-9G>APKD1Pathogenic/Likely pathogenic1621676822167682CTcriteria provided, multiple submitters, no conflicts-
DeletionNM_138694.4(PKHD1):c.3907del (p.Val1303fs)PKHD1Pathogenic65189070151890701ACAcriteria provided, single submitter-
DeletionNM_001009944.3(PKD1):c.8754_8758del (p.Gly2919fs)PKD1Pathogenic1621533002153304AGCCCGAcriteria provided, multiple submitters, no conflicts-
DeletionNM_000297.4(PKD2):c.1320-2delPKD2Pathogenic48896779288967792CACcriteria provided, single submitter-
DeletionNM_000297.4(PKD2):c.473del (p.Glu158fs)PKD2Pathogenic48892935888929358GAGcriteria provided, single submitter-
DeletionNM_138694.4(PKHD1):c.10126del (p.Ala3376fs)PKHD1Pathogenic65160921351609213GCGcriteria provided, multiple submitters, no conflicts-