RET c.1264A>G ;(p.I422V)

Variant ID: 10-43606655-A-G

NM_020975.4(RET):c.1264A>G;(p.I422V)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Somatic variants of potential clinical significance in the tumors of BRCA phenocopies.

Hereditary Cancer In Clinical Practice
Buckingham, Lela L; Mitchell, Rachel R; Maienschein-Cline, Mark M; Green, Stefan S; Hu, Vincent Hong VH; Cobleigh, Melody M; Rotmensch, Jacob J; Burgess, Kelly K; Usha, Lydia L
Publication Date: 2019

Variant appearance in text: RET: I422V
PubMed Link: 31346352
Variant Present in the following documents:
  • Main text
  • 13053_2019_Article_117.pdf
View BVdb publication page