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)
DuplicationNM_000059.4(BRCA2):c.7187dup (p.Leu2396fs)BRCA2Pathogenic133292917532929176CCTreviewed by expert panelClinGen:CA024940
single nucleotide variantNM_000059.4(BRCA2):c.71T>A (p.Leu24Ter)BRCA2Pathogenic133289321732893217TAreviewed by expert panelClinGen:CA024957
DeletionNM_000059.4(BRCA2):c.71del (p.Asp23_Leu24insTer)BRCA2Pathogenic133289321532893215ATAreviewed by expert panelClinGen:CA024955
IndelNM_000059.4(BRCA2):c.7210_7216delinsTG (p.Lys2404fs)BRCA2Pathogenic133292920032929206AAAGTCTTGreviewed by expert panelClinGen:CA024964
DeletionNM_000059.4(BRCA2):c.7211_7212del (p.Lys2404fs)BRCA2Pathogenic133292920032929201CAACreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):7439&base_change=del AA,ClinGen:CA024966
DeletionNM_000059.4(BRCA2):c.7224_7227del (p.Pro2409fs)BRCA2Pathogenic133292921432929217CACCTCreviewed by expert panelClinGen:CA024972
DeletionNM_000059.4(BRCA2):c.7226del (p.Pro2409fs)BRCA2Pathogenic133292921532929215ACAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):7454&base_change=del C,ClinGen:CA024977
InsertionNM_000059.4(BRCA2):c.7234_7235insG (p.Thr2412fs)BRCA2Pathogenic133292922432929225AAGreviewed by expert panelClinGen:CA024981
single nucleotide variantNM_000059.4(BRCA2):c.7241C>G (p.Ser2414Ter)BRCA2Pathogenic133292923132929231CGreviewed by expert panelClinGen:CA024987
single nucleotide variantNM_000059.4(BRCA2):c.7261C>T (p.Gln2421Ter)BRCA2Pathogenic133292925132929251CTreviewed by expert panelClinGen:CA025004