BRCA2 c.5082A>G ;(p.R1694=)

Variant ID: 13-32913574-A-G

NM_000059.3(BRCA2):c.5082A>G;(p.R1694=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Prevalence and clinical significance of pathogenic germline BRCA1/2 mutations in Chinese non-small cell lung cancer patients.

Cancer Biology & Medicine
Hu, Xingsheng X; Yang, Dongyong D; Li, Yalun Y; Li, Li L; Wang, Yan Y; Chen, Peng P; Xu, Song S; Pu, Xingxiang X; Zhu, Wei W; Deng, Pengbo P; Ye, Junyi J; Zhang, Hanhan H; Lizaso, Analyn A; Liu, Hao H; Mao, Xinru X; Huang, Hai H; Chu, Qian Q; Hu, Chengping C
Publication Date: 2019-08

Variant appearance in text: BRCA2: 5082A>G; Arg1694=
PubMed Link: 31565484
Variant Present in the following documents:
  • Main text
  • cbm-16-3-556.pdf
View BVdb publication page