BRCA2 c.1041dup ;(p.V348Sfs*10)

Variant ID: 13-32906654-C-CA

NM_000059.3(BRCA2):c.1041dup;(p.V348Sfs*10)

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:

Germline FFPE inherited cancer panel testing in deceased family members: implications for clinical management of unaffected relatives.

European Journal Of Human Genetics : Ejhg
Bennett, Sarah S; Alexander, Elizabeth E; Fraser, Harry H; Bowers, Naomi N; Wallace, Andrew A; Woodward, Emma R ER; Lalloo, Fiona F; Quinn, Anne Marie AM; Huang, Shuwen S; Schlecht, Helene H; Evans, D Gareth DG
Publication Date: 2021-05

Variant appearance in text: BRCA2: 1041dupA
PubMed Link: 33654310
Variant Present in the following documents:
  • 41431_2021_817_MOESM1_ESM.pdf
View BVdb publication page