Knowledge base for genomic medicine in Japanese
血友病A/B
小児・神経疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
single nucleotide variantNM_000132.4(F8):c.733C>T (p.Arg245Trp)F8Pathogenic/Likely pathogenicX154213016154213016GAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_000132.4(F8):c.558C>A (p.Asp186Glu)F8Likely pathogenicX154221254154221254GTcriteria provided, single submitter-
single nucleotide variantNM_000132.4(F8):c.460A>C (p.Thr154Pro)F8Likely pathogenicX154221352154221352TGcriteria provided, single submitter-
single nucleotide variantNM_000132.4(F8):c.143G>A (p.Arg48Lys)F8Likely pathogenicX154250685154250685CTcriteria provided, single submitter-
single nucleotide variantNM_000133.4(F9):c.88+1G>AF9Likely pathogenicX138613012138613012GAcriteria provided, single submitter-
single nucleotide variantNM_000133.4(F9):c.88+5G>TF9Likely pathogenicX138613016138613016GTcriteria provided, single submitter-
DeletionNM_000133.4(F9):c.724-5_731delF9Likely pathogenicX138642888138642900TTTGTTTTCACAGGTcriteria provided, single submitter-
single nucleotide variantNM_000132.4(F8):c.5219+2T>CF8Likely pathogenicX154156844154156844AGcriteria provided, single submitter-
DeletionNM_000133.4(F9):c.521-35_723+84delF9PathogenicX138633185138633506AAATATCAGGTTACTAATTTTTCTTCTATTTTTCTAGTGCCATTTCCATGTGGAAGAGTTTCTGTTTCACAAACTTCTAAGCTCACCCGTGCTGAGACTGTTTTTCCTGATGTGGACTATGTAAATTCTACTGAAGCTGAAACCATTTTGGATAACATCACTCAAAGCACCCAATCATTTAATGACTTCACTCGGGTTGTTGGTGGAGAAGATGCCAAACCAGGTCAATTCCCTTGGCAGGTACTTTATACTGATGGTGTGTCAAAACTGGAGCTCAGCTGGCAAGACACAGGCCAGGTGGGAGACTGAGGCTATTTTACTAGAcriteria provided, single submitter-
ComplexSingle alleleF8Likely pathogenicX154156796154227925nanacriteria provided, single submitter-