BRCA2 c.2796C>T ;(p.D932=)

Variant ID: 13-32911288-C-T

NM_000059.3(BRCA2):c.2796C>T;(p.D932=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Functional pre-therapeutic evaluation by genome editing of variants of uncertain significance of essential tumor suppressor genes.

Genome Medicine
Billaud, Amandine A; Chevalier, Louise-Marie LM; Augereau, Paule P; Frenel, Jean-Sebastien JS; Passot, Christophe C; Campone, Mario M; Morel, Alain A
Publication Date: 2021-11-09

Variant appearance in text: BRCA2: 2796C>T; Asp932=
PubMed Link: 34749799
Variant Present in the following documents:
  • 13073_2021_976_MOESM1_ESM.pdf
View BVdb publication page



A pan-cancer analysis of synonymous mutations.

Nature Communications
Sharma, Yogita Y; Miladi, Milad M; Dukare, Sandeep S; Boulay, Karine K; Caudron-Herger, Maiwen M; Groß, Matthias M; Backofen, Rolf R; Diederichs, Sven S
Publication Date: 2019-06-12

Variant appearance in text: BRCA2: 2796C>T
PubMed Link: 31189880
Variant Present in the following documents:
  • 41467_2019_10489_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page