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_138694.4(PKHD1):c.1205del (p.Phe402fs)PKHD1Likely pathogenic65192475451924754GAGcriteria provided, single submitterClinGen:CA16041070
single nucleotide variantNM_138694.4(PKHD1):c.748C>T (p.Gln250Ter)PKHD1Likely pathogenic65193428551934285GAcriteria provided, single submitterClinGen:CA16041071
single nucleotide variantNM_138694.4(PKHD1):c.603-2A>GPKHD1Likely pathogenic65193587051935870TCcriteria provided, multiple submitters, no conflictsClinGen:CA3853845
DeletionNM_138694.4(PKHD1):c.527+1delPKHD1Likely pathogenic65193826051938260ACAcriteria provided, single submitterClinGen:CA16041072
single nucleotide variantNM_138694.4(PKHD1):c.448+2T>CPKHD1Likely pathogenic65194107251941072AGcriteria provided, single submitterClinGen:CA16041073
DuplicationNM_138694.4(PKHD1):c.156dup (p.Asn53fs)PKHD1Likely pathogenic65194731451947315TTGcriteria provided, single submitterClinGen:CA16041074
DeletionNM_138694.4(PKHD1):c.4_7del (p.Thr2fs)PKHD1Likely pathogenic65194972551949728GCAGTGcriteria provided, single submitterClinGen:CA16041075
DuplicationNM_001009944.3(PKD1):c.11251_11265dup (p.Gln3751_Gln3755dup)PKD1Likely pathogenic1621424842142485CCCTGCAGCCGCACCTGcriteria provided, single submitterClinGen:CA16042936
single nucleotide variantNM_001009944.3(PKD1):c.1523G>T (p.Cys508Phe)PKD1Likely pathogenic1621669172166917CAcriteria provided, single submitterClinGen:CA16042982
DeletionNM_001009944.3(PKD1):c.8369del (p.Pro2790fs)PKD1Pathogenic/Likely pathogenic1621536892153689CGCcriteria provided, multiple submitters, no conflictsClinGen:CA16043003