BRAF c.1192_1193delinsCC ;(p.L398P)

Variant ID: 7-140482942-AA-GG

NM_004333.4(BRAF):c.1192_1193delinsCC;(p.L398P)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Validation of an NGS Panel Designed for Detection of Actionable Mutations in Tumors Common in Latin America.

Journal Of Personalized Medicine
Salvo, Mauricio M; González-Feliú, Evelin E; Toro, Jessica J; Gallegos, Iván I; Maureira, Ignacio I; Miranda-González, Nicolás N; Barajas, Olga O; Bustamante, Eva E; Ahumada, Mónica M; Colombo, Alicia A; Armisén, Ricardo R; Villamán, Camilo C; Ibañez, Carolina C; Bravo, María Loreto ML; Sanhueza, Verónica V; Spencer, M Loreto ML; de Toro, Gonzalo G; Morales, Erik E; Bizama, Carolina C; García, Patricia P; Carrasco, Ana María AM; Gutiérrez, Lorena L; Bermejo, Justo Lorenzo JL; Verdugo, Ricardo A RA; Marcelain, Katherine K
Publication Date: 2021-09-08

Variant appearance in text: BRAF: L398P
PubMed Link: 34575676
Variant Present in the following documents:
  • jpm-11-00899.pdf
View BVdb publication page