BRCA1 c.1396del ;(p.R466Gfs*9)

Variant ID: 17-41246152-CG-C

NM_007294.3(BRCA1):c.1396del;(p.R466Gfs*9)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Addition of triple negativity of breast cancer as an indicator for germline mutations in predisposing genes increases sensitivity of clinical selection criteria.

Bmc Cancer
Hoyer, Juliane J; Vasileiou, Georgia G; Uebe, Steffen S; Wunderle, Marius M; Kraus, Cornelia C; Fasching, Peter A PA; Thiel, Christian T CT; Hartmann, Arndt A; Beckmann, Matthias W MW; Lux, Michael P MP; Reis, André A
Publication Date: 2018-09-26

Variant appearance in text: BRCA1: 1396delC; Arg466Glyfs*9
PubMed Link: 30257646
Variant Present in the following documents:
  • Main text
  • 12885_2018_Article_4821.pdf
View BVdb publication page