BRCA2 c.2157T>C ;(p.N719=)

Variant ID: 13-32910649-T-C

NM_000059.3(BRCA2):c.2157T>C;(p.N719=)

This variant was identified in 1 publication

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: 2157T>C; Asn719=
PubMed Link: 34749799
Variant Present in the following documents:
  • 13073_2021_976_MOESM1_ESM.pdf
View BVdb publication page