BRAF c.1669G>A ;(p.A557T)

Variant ID: 7-140476737-C-T

NM_004333.4(BRAF):c.1669G>A;(p.A557T)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


AMLVaran: a software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting.

Bmc Medical Genomics
Wünsch, Christian C; Banck, Henrik H; Müller-Tidow, Carsten C; Dugas, Martin M
Publication Date: 2020-02-04

Variant appearance in text: BRAF: 1669G>A
PubMed Link: 32019565
Variant Present in the following documents:
  • 12920_2020_668_MOESM8_ESM.xls, sheet 1
  • 12920_2020_668_MOESM7_ESM.xls, sheet 1
View BVdb publication page