NF1 c.373_374insATGTGT ;(p.R125delinsHVC)

Variant ID: 17-29490288-C-CATGTGT

NM_001042492.2(NF1):c.373_374insATGTGT;(p.R125delinsHVC)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Exploring the somatic NF1 mutational spectrum associated with NF1 cutaneous neurofibromas.

European Journal Of Human Genetics : Ejhg
Thomas, Laura L; Spurlock, Gill G; Eudall, Claire C; Thomas, Nick S NS; Mort, Matthew M; Hamby, Stephen E SE; Chuzhanova, Nadia N; Brems, Hilde H; Legius, Eric E; Cooper, David N DN; Upadhyaya, Meena M
Publication Date: 2012-04

Variant appearance in text: NF1: 373insATGTGT
PubMed Link: 22108604
Variant Present in the following documents:
  • Main text
View BVdb publication page