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BRCA2 c.592T>C ;(p.L198=)
Variant ID: 13-32900711-T-C
NM_000059.3(
BRCA2
):c.592T>C;(p.L198=)
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:
Spatial intratumoral heterogeneity and temporal clonal evolution in esophageal squamous cell carcinoma.
Nature Genetics
Hao, Jia-Jie JJ; Lin, De-Chen DC; Dinh, Huy Q HQ; Mayakonda, Anand A; Jiang, Yan-Yi YY; Chang, Chen C; Jiang, Ye Y; Lu, Chen-Chen CC; Shi, Zhi-Zhou ZZ; Xu, Xin X; Zhang, Yu Y; Cai, Yan Y; Wang, Jin-Wu JW; Zhan, Qi-Min QM; Wei, Wen-Qiang WQ; Berman, Benjamin P BP; Wang, Ming-Rong MR; Koeffler, H Phillip HP
Publication Date: 2016-12
Variant appearance in text: BRCA2: L198L
PubMed Link:
27749841
Variant Present in the following documents:
NIHMS814330-supplement-4.xlsx, sheet 1
View BVdb publication page
Gene x Gene interaction between MnSOD and GPX-1 and breast cancer risk: a nested case-control study.
Bmc Cancer
Cox, David G DG; Tamimi, Rulla M RM; Hunter, David J DJ
Publication Date: 2006-08-31
Variant appearance in text: BRCA2: Leu198Leu
PubMed Link:
16945136
Variant Present in the following documents:
Main text
1471-2407-6-217.pdf
View BVdb publication page