BRAF c.2112A>G ;(p.R704=)

Variant ID: 7-140439627-T-C

NM_004333.4(BRAF):c.2112A>G;(p.R704=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: BRAF: R704R
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM13_ESM.xlsx, sheet 2
View BVdb publication page



Constitutive activation of the ERK pathway in melanoma and skin melanocytes in Grey horses.

Bmc Cancer
Jiang, Lin L; Campagne, Cécile C; Sundström, Elisabeth E; Sousa, Pedro P; Imran, Saima S; Seltenhammer, Monika M; Pielberg, Gerli G; Olsson, Mats J MJ; Egidy, Giorgia G; Andersson, Leif L; Golovko, Anna A
Publication Date: 2014-11-21

Variant appearance in text: BRAF: 2112A>G
PubMed Link: 25413220
Variant Present in the following documents:
  • Main text
  • 12885_2013_Article_5052.pdf
View BVdb publication page