BRAF c.787A>C ;(p.T263P)

Variant ID: 7-140501285-T-G

NM_004333.4(BRAF):c.787A>C;(p.T263P)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Whole Exome Sequencing of SMO, BRAF, PTCH1 and GNAS in Odontogenic Diseases.

In Vivo (Athens, Greece)
Shimura, Michiko M; Nakashiro, Koh-Ichi KI; Sawatani, Yuta Y; Hasegawa, Tomonori T; Kamimura, Ryota R; Izumi, Sayaka S; Komiyama, Yuske Y; Fukumoto, Chonji C; Yagisawa, Shuma S; Yaguchi, Erika E; Hitomi-Koide, Masayo M; Hyodo, Toshiki T; Uchida, Daisuke D; Kawamata, Hitoshi H
Publication Date: 2020

Variant appearance in text: BRAF: T263P
PubMed Link: 33144428
Variant Present in the following documents:
  • Main text
View BVdb publication page



Comprehensive genomic landscape and precision therapeutic approach in biliary tract cancers.

International Journal Of Cancer
Okamura, Ryosuke R; Kurzrock, Razelle R; Mallory, Robert J RJ; Fanta, Paul T PT; Burgoyne, Adam M AM; Clary, Bryan M BM; Kato, Shumei S; Sicklick, Jason K JK
Publication Date: 2021-02-01

Variant appearance in text: BRAF: T263P
PubMed Link: 32700810
Variant Present in the following documents:
  • IJC-148-702-s001.pdf
View BVdb publication page