Annotation Detail
Information
- Associated Genes
- BRCA1
- Associated Variants
-
BRCA1 p.Ser267LysfsTer19 (p.S267Kfs*19)
(
ENST00000591849.5,
ENST00000634433.2,
ENST00000618469.2,
ENST00000586385.5,
ENST00000491747.6,
ENST00000470026.6,
ENST00000644379.2,
ENST00000713676.1,
ENST00000700182.1,
ENST00000476777.6,
ENST00000489037.2,
ENST00000477152.6,
ENST00000644555.2,
ENST00000468300.5,
ENST00000473961.6,
ENST00000493795.5,
ENST00000478531.6,
ENST00000484087.6,
ENST00000494123.6,
ENST00000461574.2,
ENST00000357654.9,
ENST00000591534.5,
ENST00000497488.2,
ENST00000471181.7,
ENST00000493919.6,
ENST00000352993.7 )
BRCA1 p.Ser267LysfsTer19 (p.S267Kfs*19) ( ENST00000352993.7, ENST00000357654.9, ENST00000461574.2, ENST00000468300.5, ENST00000470026.6, ENST00000471181.7, ENST00000473961.6, ENST00000476777.6, ENST00000477152.6, ENST00000478531.6, ENST00000484087.6, ENST00000489037.2, ENST00000491747.6, ENST00000493795.5, ENST00000493919.6, ENST00000494123.6, ENST00000497488.2, ENST00000586385.5, ENST00000591534.5, ENST00000591849.5, ENST00000618469.2, ENST00000634433.2, ENST00000644379.2, ENST00000644555.2, ENST00000700182.1, ENST00000713676.1 )
BRCA1 p.Asp1799Tyr (p.D1799Y) ( ENST00000586385.5, ENST00000618469.2, ENST00000470026.6, ENST00000491747.6, ENST00000713676.1, ENST00000644379.2, ENST00000591849.5, ENST00000634433.2, ENST00000489037.2, ENST00000476777.6, ENST00000493795.5, ENST00000484087.6, ENST00000494123.6, ENST00000478531.6, ENST00000477152.6, ENST00000473961.6, ENST00000644555.2, ENST00000468300.5, ENST00000493919.6, ENST00000352993.7, ENST00000357654.9, ENST00000461574.2, ENST00000591534.5, ENST00000471181.7, ENST00000497488.2 )
BRCA1 p.Asp1799His (p.D1799H) ( ENST00000476777.6, ENST00000489037.2, ENST00000591849.5, ENST00000634433.2, ENST00000491747.6, ENST00000470026.6, ENST00000618469.2, ENST00000586385.5, ENST00000644379.2, ENST00000713676.1, ENST00000461574.2, ENST00000357654.9, ENST00000497488.2, ENST00000471181.7, ENST00000591534.5, ENST00000493919.6, ENST00000352993.7, ENST00000477152.6, ENST00000644555.2, ENST00000468300.5, ENST00000473961.6, ENST00000493795.5, ENST00000478531.6, ENST00000484087.6, ENST00000494123.6 )
BRCA1 p.Asp1799Asn (p.D1799N) ( ENST00000352993.7, ENST00000357654.9, ENST00000468300.5, ENST00000591534.5, ENST00000471181.7, ENST00000591849.5, ENST00000586385.5, ENST00000493795.5, ENST00000491747.6, ENST00000461574.2, ENST00000470026.6, ENST00000473961.6, ENST00000476777.6, ENST00000477152.6, ENST00000478531.6, ENST00000484087.6, ENST00000489037.2, ENST00000493919.6, ENST00000494123.6, ENST00000497488.2, ENST00000618469.2, ENST00000634433.2, ENST00000644379.2, ENST00000644555.2, ENST00000713676.1 )
BRCA1 p.Asp1799Tyr (p.D1799Y) ( ENST00000352993.7, ENST00000357654.9, ENST00000461574.2, ENST00000468300.5, ENST00000470026.6, ENST00000471181.7, ENST00000473961.6, ENST00000476777.6, ENST00000477152.6, ENST00000478531.6, ENST00000484087.6, ENST00000489037.2, ENST00000491747.6, ENST00000493795.5, ENST00000493919.6, ENST00000494123.6, ENST00000497488.2, ENST00000586385.5, ENST00000591534.5, ENST00000591849.5, ENST00000618469.2, ENST00000634433.2, ENST00000644379.2, ENST00000644555.2, ENST00000713676.1 )
BRCA1 p.Asp1799His (p.D1799H) ( ENST00000352993.7, ENST00000357654.9, ENST00000461574.2, ENST00000468300.5, ENST00000470026.6, ENST00000471181.7, ENST00000473961.6, ENST00000476777.6, ENST00000477152.6, ENST00000478531.6, ENST00000484087.6, ENST00000489037.2, ENST00000491747.6, ENST00000493795.5, ENST00000493919.6, ENST00000494123.6, ENST00000497488.2, ENST00000586385.5, ENST00000591534.5, ENST00000591849.5, ENST00000618469.2, ENST00000634433.2, ENST00000644379.2, ENST00000644555.2, ENST00000713676.1 )
BRCA1 p.Asp1799Asn (p.D1799N) ( ENST00000352993.7, ENST00000357654.9, ENST00000461574.2, ENST00000468300.5, ENST00000470026.6, ENST00000471181.7, ENST00000473961.6, ENST00000476777.6, ENST00000477152.6, ENST00000478531.6, ENST00000484087.6, ENST00000489037.2, ENST00000491747.6, ENST00000493795.5, ENST00000493919.6, ENST00000494123.6, ENST00000497488.2, ENST00000586385.5, ENST00000591534.5, ENST00000591849.5, ENST00000618469.2, ENST00000634433.2, ENST00000644379.2, ENST00000644555.2, ENST00000713676.1 ) - Associated Disease
- Malignant neoplasm of breast
- Source Database
- DisGeNET
- Description
- The rare BRCA1 UV c.5332G>A/p.Asp1778Asn was found here for the first time in co-occurrence in trans with the deleterious BRCA1 mutation c.798_799delTT/p.Ser267LysfsX19 in young breast cancer patient.
- Pubmed
- 22684231
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.36
- Year of publication
- 2012
Drugs