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.10377C>G (p.Tyr3459Ter)PKD1Likely pathogenic1621473482147348GCcriteria provided, single submitter-
DeletionNM_001009944.3(PKD1):c.10247del (p.Gly3416fs)PKD1Likely pathogenic1621474782147478TCTcriteria provided, single submitter-
DeletionNM_001009944.3(PKD1):c.9826_9829del (p.Thr3276fs)PKD1Likely pathogenic1621499562149959CGAGTCcriteria provided, single submitter-
single nucleotide variantNM_001009944.3(PKD1):c.9431G>C (p.Gly3144Ala)PKD1Likely pathogenic1621505342150534CGcriteria provided, single submitter-
single nucleotide variantNM_001009944.3(PKD1):c.9298C>T (p.Gln3100Ter)PKD1Pathogenic/Likely pathogenic1621521612152161GAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_001009944.3(PKD1):c.8973C>A (p.Tyr2991Ter)PKD1Pathogenic/Likely pathogenic1621526102152610GTcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_001009944.3(PKD1):c.8933T>C (p.Phe2978Ser)PKD1Likely pathogenic1621528302152830AGcriteria provided, single submitter-
single nucleotide variantNM_001009944.3(PKD1):c.7984C>T (p.Gln2662Ter)PKD1Pathogenic/Likely pathogenic1621553552155355GAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_001009944.3(PKD1):c.7915C>T (p.Arg2639Ter)PKD1Pathogenic1621554242155424GAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_001009944.3(PKD1):c.7856T>G (p.Leu2619Arg)PKD1Likely pathogenic1621558732155873ACcriteria provided, single submitter-