Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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