BRCA2 c.1035_1036insT ;(p.N346*)

Variant ID: 13-32906650-A-AT

NM_000059.3(BRCA2):c.1035_1036insT;(p.N346*)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Main implications related to the switch to BRCA1/2 tumor testing in ovarian cancer patients: a proposal of a consensus.

Oncotarget
Capoluongo, Ettore E; Scambia, Giovanni G; Nabholtz, Jean-Marc JM
Publication Date: 2018-04-13

Variant appearance in text: BRCA2: Asn346fs
PubMed Link: 29731958
Variant Present in the following documents:
  • Main text
  • oncotarget-09-19463.pdf
View BVdb publication page



The frequency of cancer predisposition gene mutations in hereditary breast and ovarian cancer patients in Taiwan: From BRCA1/2 to multi-gene panels.

Plos One
Sung, Pi-Lin PL; Wen, Kuo-Chang KC; Chen, Yi-Jen YJ; Chao, Ta-Chung TC; Tsai, Yi-Fang YF; Tseng, Ling-Ming LM; Qiu, Jian-Tai Timothy JT; Chao, Kuan-Chong KC; Wu, Hua-Hsi HH; Chuang, Chi-Mu CM; Wang, Peng-Hui PH; Huang, Chi-Ying F CF
Publication Date: 2017

Variant appearance in text: N/A
PubMed Link: 28961279
Variant Present in the following documents:
View BVdb publication page