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BRCA2 c.2913A>G ;(p.L971=)
Variant ID: 13-32911405-A-G
NM_000059.3(
BRCA2
):c.2913A>G;(p.L971=)
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:
Sequencing of BRCA1/2-alterations using NGS-based technology: annotation as a challenge.
Oncotarget
Ebner, Silvana S; Winkelmann, Ria R; Martin, Saskia S; Köllermann, Jens J; Wild, Peter J PJ; Demes, Melanie M
Publication Date: 2022
Variant appearance in text: BRCA2: 2913A>G
PubMed Link:
35251494
Variant Present in the following documents:
Main text
oncotarget-13-28213.pdf
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: L971L
PubMed Link:
33691754
Variant Present in the following documents:
13059_2021_2305_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page