Knowledge base for genomic medicine in Japanese
ウィルムス腫瘍
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DuplicationNM_000059.4(BRCA2):c.6652dup (p.Asp2218fs)BRCA2Pathogenic133291514332915144AAGreviewed by expert panelClinGen:CA024258
single nucleotide variantNM_000059.4(BRCA2):c.6656C>G (p.Ser2219Ter)BRCA2Pathogenic133291514832915148CGreviewed by expert panelClinGen:CA024263
DeletionNM_000059.4(BRCA2):c.6658_6661del (p.Glu2220fs)BRCA2Pathogenic133291514932915152CAGAACreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):6886&base_change=del GAAA,ClinGen:CA024265
DeletionNM_000059.4(BRCA2):c.6673del (p.Thr2225fs)BRCA2Pathogenic133291516332915163GAGreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):6901&base_change=del A,ClinGen:CA024273
DeletionNM_000059.4(BRCA2):c.6676_6677del (p.Glu2226fs)BRCA2Pathogenic133291516732915168CAGCreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):6904&base_change=del GA,ClinGen:CA024279
DeletionNM_000059.4(BRCA2):c.6678del (p.Ala2227fs)BRCA2Pathogenic133291516932915169GAGreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):6906&base_change=del A,ClinGen:CA024281
DuplicationNM_000059.4(BRCA2):c.6682dup (p.Val2228fs)BRCA2Pathogenic133291517332915174AAGreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):6910&base_change=ins G,ClinGen:CA024285
DeletionNM_000059.4(BRCA2):c.6684del (p.Glu2229fs)BRCA2Pathogenic133291517632915176TATreviewed by expert panelClinGen:CA024290
DeletionNM_000059.4(BRCA2):c.6688del (p.Ile2230fs)BRCA2Pathogenic133291517832915178GAGreviewed by expert panelClinGen:CA024296
single nucleotide variantNM_000059.4(BRCA2):c.67+1G>ABRCA2Pathogenic133289066532890665GAcriteria provided, multiple submitters, no conflictsBreast Cancer Information Core (BIC) (BRCA2):295+1&base_change=G to A,ClinGen:CA024334