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BRCA2 c.366dup ;(p.K123*)
Variant ID: 13-32899261-C-CT
NM_000059.3(
BRCA2
):c.366dup;(p.K123*)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Pathogenic germline BRCA1/2 mutations and familial predisposition to gastric cancer.
Jco Precision Oncology
Ichikawa, Hiroshi H; Wakai, Toshifumi T; Nagahashi, Masayuki M; Shimada, Yoshifumi Y; Hanyu, Takaaki T; Kano, Yosuke Y; Muneoka, Yusuke Y; Ishikawa, Takashi T; Takizawa, Kazuyasu K; Tajima, Yosuke Y; Sakata, Jun J; Kobayashi, Takashi T; Kemeyama, Hitoshi H; Yabusaki, Hiroshi H; Nakagawa, Satoru S; Sato, Nobuaki N; Kawasaki, Takashi T; Homma, Keiichi K; Okuda, Shujiro S; Lyle, Stephen S; Takabe, Kazuaki K
Publication Date: 2018
Variant appearance in text: BRCA2: K123fs
PubMed Link:
31608315
Variant Present in the following documents:
Main text
PO.18.00097.pdf
View BVdb publication page