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)
DeletionNM_000059.4(BRCA2):c.8575del (p.Gln2859fs)BRCA2Pathogenic133294518032945180ACAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):8803&base_change=del C,ClinGen:CA025719
DuplicationNM_000059.4(BRCA2):c.8585dup (p.Glu2863fs)BRCA2Pathogenic133294518932945190CCTreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):8813&base_change=ins T,ClinGen:CA025723
single nucleotide variantNM_000059.4(BRCA2):c.8633-2A>GBRCA2Pathogenic133295080532950805AGreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):8861-2&base_change=A to G,ClinGen:CA025749
single nucleotide variantNM_000059.4(BRCA2):c.8677C>T (p.Gln2893Ter)BRCA2Pathogenic133295085132950851CTreviewed by expert panelClinGen:CA025776
DeletionNM_000059.4(BRCA2):c.8680del (p.Gln2894fs)BRCA2Pathogenic133295085432950854GCGreviewed by expert panelClinGen:CA025779
single nucleotide variantNM_000059.4(BRCA2):c.8695C>T (p.Gln2899Ter)BRCA2Pathogenic133295086932950869CTreviewed by expert panelClinGen:CA025783
single nucleotide variantNM_000059.4(BRCA2):c.8754+5G>ABRCA2Pathogenic/Likely pathogenic133295093332950933GAcriteria provided, multiple submitters, no conflictsBreast Cancer Information Core (BIC) (BRCA2):8982+5&base_change=G to A,ClinGen:CA025807
single nucleotide variantNM_000059.4(BRCA2):c.8755-1G>ABRCA2Pathogenic133295345332953453GAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):8983-1&base_change=G to A,ClinGen:CA025812
single nucleotide variantNM_000059.4(BRCA2):c.8869C>T (p.Gln2957Ter)BRCA2Pathogenic133295356832953568CTreviewed by expert panelClinGen:CA025856
DeletionNM_000059.4(BRCA2):c.8904del (p.Val2969fs)BRCA2Pathogenic133295360232953602ACAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):9132&base_change=del C,ClinGen:CA025865