BRCA2 c.317-22C>T

Variant ID: 13-32899191-C-T

NM_000059.3(BRCA2):c.317-22C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic epidemiology of BRCA1- and BRCA2-associated cancer across Latin America.

Npj Breast Cancer
Herzog, Josef S JS; Chavarri-Guerra, Yanin Y; Castillo, Danielle D; Abugattas, Julio J; Villarreal-Garza, Cynthia C; Sand, Sharon S; Clague-Dehart, Jessica J; Alvarez-Gómez, Rosa M RM; Wegman-Ostrosky, Talia T; Mohar, Alejandro A; Mora, Pamela P; Del Toro-Valero, Azucena A; Daneri-Navarro, Adrian A; Rodriguez, Yenni Y; Cruz-Correa, Marcia M; Ashton-Prolla, Patricia P; Alemar, Bárbara B; Mejia, Rosa R; Gallardo, Lenny L; Shaw, Robin R; Yang, Kai K; Cervantes, Aleck A; Tsang, Kevin K; Nehoray, Bita B; Barrera Saldana, Hugo H; Neuhausen, Susan S; Weitzel, Jeffrey N JN
Publication Date: 2021-08-19

Variant appearance in text: BRCA2: 317-22C>T; rs81002794
PubMed Link: 34413315
Variant Present in the following documents:
  • 41523_2021_317_MOESM1_ESM.xlsx, sheet 2
View BVdb publication page



Globally Rare BRCA2 Variants With Founder Haplotypes in the South African Population: Implications for Point-of-Care Testing Based on a Single-Institution BRCA1/2 Next-Generation Sequencing Study.

Frontiers In Oncology
Oosthuizen, Jaco J; Kotze, Maritha J MJ; Van Der Merwe, Nicole N; Myburgh, Ettienne J EJ; Bester, Phillip P; van der Merwe, Nerina C NC
Publication Date: 2020

Variant appearance in text: BRCA2: 317-22C>T; rs81002794
PubMed Link: 33643918
Variant Present in the following documents:
  • Main text
  • fonc-10-619469.pdf
View BVdb publication page