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_007294.4(BRCA1):c.5332G>A (p.Asp1778Asn)BRCA1Pathogenic/Likely pathogenic174120308041203080CTcriteria provided, multiple submitters, no conflictsClinGen:CA003491
single nucleotide variantNM_007294.4(BRCA1):c.5333-1G>ABRCA1Pathogenic/Likely pathogenic174120121241201212CTcriteria provided, multiple submitters, no conflictsClinGen:CA003494
single nucleotide variantNM_007294.4(BRCA1):c.5333-1G>CBRCA1Pathogenic/Likely pathogenic174120121241201212CGcriteria provided, multiple submitters, no conflictsBreast Cancer Information Core (BIC) (BRCA1):5452-1&base_change=G to C,ClinGen:CA003496
single nucleotide variantNM_007294.4(BRCA1):c.5333-2A>CBRCA1Pathogenic174120121341201213TGcriteria provided, single submitterClinGen:CA003497
single nucleotide variantNM_007294.4(BRCA1):c.5333-2A>TBRCA1Pathogenic/Likely pathogenic174120121341201213TAcriteria provided, multiple submitters, no conflictsClinGen:CA003498
single nucleotide variantNM_007294.4(BRCA1):c.5333-3T>GBRCA1Pathogenic174120121441201214ACcriteria provided, single submitterClinGen:CA003499
single nucleotide variantNM_007294.4(BRCA1):c.5335C>T (p.Gln1779Ter)BRCA1Pathogenic174120120941201209GAreviewed by expert panelClinGen:CA003506
single nucleotide variantNM_007294.4(BRCA1):c.5339T>C (p.Leu1780Pro)BRCA1Pathogenic/Likely pathogenic174120120541201205AGcriteria provided, multiple submitters, no conflictsClinGen:CA003508
single nucleotide variantNM_007294.4(BRCA1):c.5341G>T (p.Glu1781Ter)BRCA1Pathogenic174120120341201203CAreviewed by expert panelClinGen:CA003511
DeletionNM_007294.4(BRCA1):c.5341del (p.Glu1781fs)BRCA1Pathogenic174120120341201203TCTreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA1):5460&base_change=del G,ClinGen:CA003510