BRAF c.113C>T ;(p.A38V)

Variant ID: 7-140624391-G-A

NM_004333.4(BRAF):c.113C>T;(p.A38V)

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:

Rare germline variants in DNA repair-related genes are accountable for papillary thyroid cancer susceptibility.

Endocrine
Mio, Catia C; Verrienti, Antonella A; Pecce, Valeria V; Sponziello, Marialuisa M; Damante, Giuseppe G
Publication Date: 2021-09

Variant appearance in text: BRAF: 113C>T; A38V
PubMed Link: 33821390
Variant Present in the following documents:
  • 12020_2021_Article_2705.pdf
View BVdb publication page