Knowledge base for genomic medicine in Japanese
家族性膵がん
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DeletionNM_000059.4(BRCA2):c.6761_6762del (p.Phe2254fs)BRCA2Pathogenic133291525032915251CTTCreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):6989&base_change=del TT,ClinGen:CA024383
single nucleotide variantNM_000059.4(BRCA2):c.6768T>A (p.Cys2256Ter)BRCA2Pathogenic133291526032915260TAreviewed by expert panelClinGen:CA024394
single nucleotide variantNM_000059.4(BRCA2):c.67G>T (p.Asp23Tyr)BRCA2Pathogenic/Likely pathogenic133289066432890664GTcriteria provided, multiple submitters, no conflictsClinGen:CA024413
single nucleotide variantNM_000059.4(BRCA2):c.6800C>A (p.Ser2267Ter)BRCA2Pathogenic133291529232915292CAreviewed by expert panelClinGen:CA024416
DeletionNM_000059.4(BRCA2):c.6809del (p.Gly2270fs)BRCA2Pathogenic133291530032915300TGTreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):7037&base_change=del G,ClinGen:CA024424
single nucleotide variantNM_000059.4(BRCA2):c.681+4A>GBRCA2Pathogenic/Likely pathogenic133290363332903633AGcriteria provided, multiple submitters, no conflictsClinGen:CA024432
DeletionNM_000059.4(BRCA2):c.6814del (p.Arg2272fs)BRCA2Pathogenic133291530232915302GAGreviewed by expert panelClinGen:CA024434
DeletionNM_000059.4(BRCA2):c.6816_6817del (p.Gly2274fs)BRCA2Pathogenic133291530832915309GAAGreviewed by expert panelClinGen:CA024440
single nucleotide variantNM_000059.4(BRCA2):c.682-1G>CBRCA2Pathogenic/Likely pathogenic133290505532905055GCcriteria provided, multiple submitters, no conflictsBreast Cancer Information Core (BIC) (BRCA2):910-1&base_change=G to C,ClinGen:CA024456
DeletionNM_000059.4(BRCA2):c.6833_6837del (p.Ile2278fs)BRCA2Pathogenic133291532132915325CCTTATCreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):7057&base_change=del CTTAT,Breast Cancer Information Core (BIC) (BRCA2):7061&base_change=del TCTTA,ClinGen:CA024468