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.756_759del (p.Asp252fs)BRCA2Pathogenic133290513032905133ACAGTAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):984&base_change=del CAGT,ClinGen:CA025156
DeletionNM_000059.4(BRCA2):c.7593del (p.Ser2533fs)BRCA2Pathogenic133293072132930721GTGreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):7821&base_change=del T,ClinGen:CA025166
single nucleotide variantNM_000059.4(BRCA2):c.7612A>T (p.Lys2538Ter)BRCA2Pathogenic133293074132930741ATreviewed by expert panelClinGen:CA025180
single nucleotide variantNM_000059.4(BRCA2):c.7617+1G>ABRCA2Pathogenic133293074732930747GAreviewed by expert panelClinGen:CA025182
single nucleotide variantNM_000059.4(BRCA2):c.7617+1G>TBRCA2Pathogenic/Likely pathogenic133293074732930747GTcriteria provided, multiple submitters, no conflictsClinGen:CA025183
single nucleotide variantNM_000059.4(BRCA2):c.7617+2T>GBRCA2Pathogenic133293074832930748TGreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):7845+2&base_change=T to G,ClinGen:CA025184
DeletionNM_000059.4(BRCA2):c.7636_7645del (p.Ser2546fs)BRCA2Pathogenic133293189532931904GTTTCTAAACAGreviewed by expert panelClinGen:CA025203
single nucleotide variantNM_000059.4(BRCA2):c.7647C>A (p.Cys2549Ter)BRCA2Pathogenic133293190832931908CAreviewed by expert panelClinGen:CA025210
DeletionNM_000059.4(BRCA2):c.7655_7658del (p.Ile2552fs)BRCA2Pathogenic133293191432931917AAATTAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):7883&base_change=del TTAA,ClinGen:CA025214
DeletionNM_000059.4(BRCA2):c.7671del (p.Glu2558fs)BRCA2Pathogenic133293193232931932CACreviewed by expert panelClinGen:CA025216