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BRCA2 c.117T>C ;(p.A39=)
Variant ID: 13-32893263-T-C
NM_000059.3(
BRCA2
):c.117T>C;(p.A39=)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Identifying Sequence Variants of 18 Hereditary Ovarian Cancer-Associated Genes in Chinese Epithelial Ovarian Cancer Patients.
Biomed Research International
Wu, Xiao X; Chen, Zhengzheng Z; Ren, Pingping P; Zhao, Xuxu X; Tang, Dongdong D; Geng, Hao H; Xu, Xiaofeng X; Zhao, Weidong W
Publication Date: 2021
Variant appearance in text: BRCA2: A39A
PubMed Link:
34350294
Variant Present in the following documents:
Main text
View BVdb publication page
Identification of pathogenic variants in cancer genes using base editing screens with editing efficiency correction.
Genome Biology
Huang, Changcai C; Li, Guangyu G; Wu, Jiayu J; Liang, Junbo J; Wang, Xiaoyue X
Publication Date: 2021-03-10
Variant appearance in text: BRCA2: A39A
PubMed Link:
33691754
Variant Present in the following documents:
13059_2021_2305_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page