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)
single nucleotide variantNM_024675.4(PALB2):c.48+2T>GPALB2Likely pathogenic162365242923652429ACcriteria provided, single submitterClinGen:CA10580057
DeletionNM_024675.4(PALB2):c.35del (p.Glu12fs)PALB2Pathogenic162365244423652444CTCcriteria provided, multiple submitters, no conflictsClinGen:CA10580061
DeletionNM_007294.4(BRCA1):c.5328del (p.Thr1777fs)BRCA1Pathogenic174120308441203084TGTreviewed by expert panelClinGen:CA10580487
DeletionNM_007294.4(BRCA1):c.5236del (p.His1746fs)BRCA1Pathogenic174120911041209110TGTreviewed by expert panelClinGen:CA10580492
DeletionNM_007294.4(BRCA1):c.5202del (p.Phe1734fs)BRCA1Pathogenic174120914441209144CACreviewed by expert panelClinGen:CA10580494
DeletionNM_007294.4(BRCA1):c.5176del (p.Arg1726fs)BRCA1Pathogenic174121536741215367CTCreviewed by expert panelClinGen:CA10580497
single nucleotide variantNM_007294.4(BRCA1):c.5135G>A (p.Trp1712Ter)BRCA1Pathogenic174121590841215908CTreviewed by expert panelClinGen:CA10580498
DuplicationNM_007294.4(BRCA1):c.4997dup (p.Tyr1666Ter)BRCA1Pathogenic174121970141219702GGTreviewed by expert panelClinGen:CA10580503
DeletionNM_007294.4(BRCA1):c.4654_4673del (p.Tyr1552fs)BRCA1Pathogenic174122635041226369TAGATCTTGCCTTGGCAAGTATreviewed by expert panelClinGen:CA10580512
single nucleotide variantNM_007294.4(BRCA1):c.4432G>T (p.Glu1478Ter)BRCA1Pathogenic174122855741228557CAreviewed by expert panelClinGen:CA10580519