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.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-
single nucleotide variantNM_001009944.3(PKD1):c.7587G>C (p.Lys2529Asn)PKD1Likely pathogenic1621562082156208CGcriteria provided, single submitter-
DeletionNM_001009944.3(PKD1):c.5411del (p.Gly1804fs)PKD1Likely pathogenic1621597572159757GCGcriteria provided, single submitter-
single nucleotide variantNM_001009944.3(PKD1):c.5279G>A (p.Trp1760Ter)PKD1Likely pathogenic1621598892159889CTcriteria provided, single submitter-
single nucleotide variantNM_001009944.3(PKD1):c.4957C>T (p.Gln1653Ter)PKD1Pathogenic/Likely pathogenic1621602112160211GAcriteria provided, multiple submitters, no conflicts-