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)
DuplicationNM_138694.4(PKHD1):c.9723dup (p.Gly3242fs)PKHD1Pathogenic65161269051612691CCAcriteria provided, single submitter-
single nucleotide variantNM_138694.4(PKHD1):c.9619G>A (p.Ala3207Thr)PKHD1Pathogenic/Likely pathogenic65161279551612795CTcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_138694.4(PKHD1):c.9003C>G (p.Tyr3001Ter)PKHD1Pathogenic65161341151613411GCcriteria provided, single submitter-
DeletionNM_138694.4(PKHD1):c.7973_7977del (p.Leu2658fs)PKHD1Pathogenic65171270351712707GCGGCAGcriteria provided, single submitter-
DeletionNM_138694.4(PKHD1):c.7888del (p.Leu2630fs)PKHD1Pathogenic65172071451720714AGAcriteria provided, single submitter-
DeletionNM_138694.4(PKHD1):c.7811_7827del (p.Arg2604fs)PKHD1Pathogenic65172077551720791GGTTAGACAATGTATCACGcriteria provided, single submitter-
DeletionNM_138694.4(PKHD1):c.5665del (p.Glu1889fs)PKHD1Pathogenic65187519351875193TCTcriteria provided, single submitter-
IndelNM_138694.4(PKHD1):c.4492_4494delinsAG (p.Ser1498_Leu1499insTer)PKHD1Pathogenic/Likely pathogenic65189011451890116AGACTcriteria provided, multiple submitters, no conflicts-
DuplicationNM_138694.4(PKHD1):c.2310dup (p.Ser771fs)PKHD1Pathogenic65191338651913387AATcriteria provided, single submitter-
IndelNM_138694.4(PKHD1):c.2176_2177delinsT (p.Gly726fs)PKHD1Pathogenic65191505751915058CCAcriteria provided, single submitter-