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.8340_8343del (p.Asn2781fs)BRCA2Pathogenic133294454632944549GCTAAGreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):8568&base_change=del TAAC,ClinGen:CA025590
DeletionNM_000059.4(BRCA2):c.8343del (p.Asn2781fs)BRCA2Pathogenic133294455032944550ACAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):8571&base_change=del C,ClinGen:CA025591
DuplicationNM_000059.4(BRCA2):c.8348dup (p.Arg2784fs)BRCA2Pathogenic133294455432944555AACreviewed by expert panelClinGen:CA025592
single nucleotide variantNM_000059.4(BRCA2):c.8363G>A (p.Trp2788Ter)BRCA2Pathogenic133294457032944570GAreviewed by expert panelClinGen:CA025603
single nucleotide variantNM_000059.4(BRCA2):c.8363G>C (p.Trp2788Ser)BRCA2Likely pathogenic133294457032944570GCcriteria provided, multiple submitters, no conflictsClinGen:CA025604
single nucleotide variantNM_000059.4(BRCA2):c.8364G>A (p.Trp2788Ter)BRCA2Pathogenic133294457132944571GAreviewed by expert panelClinGen:CA025605
single nucleotide variantNM_000059.4(BRCA2):c.8377G>A (p.Gly2793Arg)BRCA2Pathogenic/Likely pathogenic133294458432944584GAcriteria provided, multiple submitters, no conflictsClinGen:CA025613
IndelNM_000059.4(BRCA2):c.8394_8396delinsAA (p.Arg2799fs)BRCA2Pathogenic133294460132944603TAGAAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):8622&base_change=del TAG ins AA,ClinGen:CA025623
DeletionNM_000059.4(BRCA2):c.8395del (p.Arg2799fs)BRCA2Pathogenic133294460232944602TATreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):8623&base_change=del A,ClinGen:CA025624
DeletionNM_000059.4(BRCA2):c.8415_8416del (p.Leu2805fs)BRCA2Pathogenic133294462132944622TTATreviewed by expert panelClinGen:CA025631