BRCA2 c.969_970insC ;(p.R324Qfs*3)

Variant ID: 13-32906584-A-AC

NM_000059.3(BRCA2):c.969_970insC;(p.R324Qfs*3)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countries.

Journal Of Medical Genetics
Kwong, Ava A; Shin, Vivian Y VY; Ho, John C W JC; Kang, Eunyoung E; Nakamura, Seigo S; Teo, Soo-Hwang SH; Lee, Ann S G AS; Sng, Jen-Hwei JH; Ginsburg, Ophira M OM; Kurian, Allison W AW; Weitzel, Jeffrey N JN; Siu, Man-Ting MT; Law, Fian B F FB; Chan, Tsun-Leung TL; Narod, Steven A SA; Ford, James M JM; Ma, Edmond S K ES; Kim, Sung-Won SW
Publication Date: 2016-01

Variant appearance in text: BRCA2: 969_970insC
PubMed Link: 26187060
Variant Present in the following documents:
  • Main text
View BVdb publication page