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_007294.4(BRCA1):c.1227_1230dup (p.Asp411delinsSerTer)BRCA1Pathogenic174124631741246318CCAGCTreviewed by expert panelClinGen:CA10589957
single nucleotide variantNM_007294.4(BRCA1):c.1222A>T (p.Lys408Ter)BRCA1Pathogenic174124632641246326TAreviewed by expert panelClinGen:CA10589958
InsertionNM_007294.4(BRCA1):c.1210_1211insCT (p.Glu404fs)BRCA1Pathogenic174124633741246338TTAGreviewed by expert panelClinGen:CA10589959
DeletionNM_007294.4(BRCA1):c.1209_1210del (p.Glu404fs)BRCA1Pathogenic174124633841246339TCATreviewed by expert panelClinGen:CA10589960
DuplicationNM_007294.4(BRCA1):c.1209dup (p.Glu404Ter)BRCA1Pathogenic174124633841246339CCAreviewed by expert panelClinGen:CA10589961
InsertionNM_007294.4(BRCA1):c.1179_1180insT (p.Gly394fs)BRCA1Pathogenic174124636841246369CCAreviewed by expert panelClinGen:CA10589962
DeletionNM_007294.4(BRCA1):c.1174del (p.Leu392fs)BRCA1Pathogenic174124637441246374AGAreviewed by expert panelClinGen:CA10589963
single nucleotide variantNM_007294.4(BRCA1):c.1171G>T (p.Glu391Ter)BRCA1Pathogenic174124637741246377CAreviewed by expert panelClinGen:CA10589964
DeletionNM_007294.4(BRCA1):c.1140del (p.Val382fs)BRCA1Pathogenic174124640841246408TCTreviewed by expert panelClinGen:CA10589965
DeletionNM_007294.4(BRCA1):c.1125_1132del (p.Asn376fs)BRCA1Pathogenic174124641641246423CTGCTATTTCreviewed by expert panelClinGen:CA10589966