BRCA2 c.1659A>G ;(p.L553=)

Variant ID: 13-32907274-A-G

NM_000059.3(BRCA2):c.1659A>G;(p.L553=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Toward automation of germline variant curation in clinical cancer genetics.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Ravichandran, Vignesh V; Shameer, Zarina Z; Kemel, Yelena Y; Walsh, Michael M; Cadoo, Karen K; Lipkin, Steven S; Mandelker, Diana D; Zhang, Liying L; Stadler, Zsofia Z; Robson, Mark M; Offit, Kenneth K; Vijai, Joseph J
Publication Date: 2019-09

Variant appearance in text: BRCA2: 1659A>G
PubMed Link: 30787465
Variant Present in the following documents:
  • NIHMS1525468-supplement-Large_Excel_File.xlsx, sheet 6
View BVdb publication page



Prevalence of PALB2 mutations in breast cancer patients in multi-ethnic Asian population in Malaysia and Singapore.

Plos One
Phuah, Sze Yee SY; Lee, Sheau Yee SY; Kang, Peter P; Kang, In Nee IN; Yoon, Sook-Yee SY; Thong, Meow Keong MK; Hartman, Mikael M; Sng, Jen-Hwei JH; Yip, Cheng Har CH; Taib, Nur Aishah Mohd NA; Teo, Soo-Hwang SH
Publication Date: 2013

Variant appearance in text: BRCA2: 1659A>G
PubMed Link: 23977390
Variant Present in the following documents:
  • Main text
  • pone.0073638.pdf
View BVdb publication page