BRCA2 c.1623A>G ;(p.E541=)

Variant ID: 13-32907238-A-G

NM_000059.3(BRCA2):c.1623A>G;(p.E541=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


TumorNext-Lynch-MMR: a comprehensive next generation sequencing assay for the detection of germline and somatic mutations in genes associated with mismatch repair deficiency and Lynch syndrome.

Oncotarget
Gray, Phillip N PN; Tsai, Pei P; Chen, Daniel D; Wu, Sitao S; Hoo, Jayne J; Mu, Wenbo W; Li, Bing B; Vuong, Huy H; Lu, Hsiao-Mei HM; Batth, Navanjot N; Willett, Sara S; Uyeda, Lisa L; Shah, Swati S; Gau, Chia-Ling CL; Umali, Monalyn M; Espenschied, Carin C; Janicek, Mike M; Brown, Sandra S; Margileth, David D; Dobrea, Lavinia L; Wagman, Lawrence L; Rana, Huma H; Hall, Michael J MJ; Ross, Theodora T; Terdiman, Jonathan J; Cullinane, Carey C; Ries, Savita S; Totten, Ellen E; Elliott, Aaron M AM
Publication Date: 2018-04-17

Variant appearance in text: BRCA2: E541E
PubMed Link: 29755653
Variant Present in the following documents:
  • oncotarget-09-20304-s001.pdf
View BVdb publication page