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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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