BRCA2 c.2001G>C ;(p.L667=)

Variant ID: 13-32910493-G-C

NM_000059.3(BRCA2):c.2001G>C;(p.L667=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: L667L
PubMed Link: 33691754
Variant Present in the following documents:
  • 13059_2021_2305_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page



Inherited predisposition to breast cancer in the Carolina Breast Cancer Study.

Npj Breast Cancer
Walsh, Tom T; Gulsuner, Suleyman S; Lee, Ming K MK; Troester, Melissa A MA; Olshan, Andrew F AF; Earp, H Shelton HS; Perou, Charles M CM; King, Mary-Claire MC
Publication Date: 2021-01-21

Variant appearance in text: BRCA2: 2001G>C
PubMed Link: 33479248
Variant Present in the following documents:
  • 41523_2020_214_MOESM1_ESM.pdf
View BVdb publication page