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BRCA2 c.2059_2061delinsTAA ;(p.D687*)
Variant ID: 13-32910551-GAT-TAA
NM_000059.3(
BRCA2
):c.2059_2061delinsTAA;(p.D687*)
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:
Prevalence of BRCA1 and BRCA2 Mutations Among Patients With Ovarian, Primary Peritoneal, and Fallopian Tube Cancer in India: A Multicenter Cross-Sectional Study.
Jco Global Oncology
Gupta, Sudeep S; Rajappa, Senthil S; Advani, Suresh S; Agarwal, Amit A; Aggarwal, Shyam S; Goswami, Chanchal C; Palanki, Satya Dattatreya SD; Arya, Devavrat D; Patil, Shekhar S; Kodagali, Rohit R
Publication Date: 2021-06
Variant appearance in text: BRCA2: Asp687ter
PubMed Link:
34101484
Variant Present in the following documents:
go-7-go.21.00051.pdf
View BVdb publication page
Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.
Plos One
LaDuca, Holly H; Farwell, Kelly D KD; Vuong, Huy H; Lu, Hsiao-Mei HM; Mu, Wenbo W; Shahmirzadi, Layla L; Tang, Sha S; Chen, Jefferey J; Bhide, Shruti S; Chao, Elizabeth C EC
Publication Date: 2017
Variant appearance in text: BRCA2: D687*
PubMed Link:
28152038
Variant Present in the following documents:
pone.0170843.s003.xlsx, sheet 1
View BVdb publication page