NRAS c.64_65delinsGT ;(p.Q22V)

Variant ID: 1-115258717-TG-AC

NM_002524.4(NRAS):c.64_65delinsGT;(p.Q22V)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Assessment of computational methods for predicting the effects of missense mutations in human cancers.

Bmc Genomics
Gnad, Florian F; Baucom, Albion A; Mukhyala, Kiran K; Manning, Gerard G; Zhang, Zemin Z
Publication Date: 2013

Variant appearance in text: NRAS: Q22V
PubMed Link: 23819521
Variant Present in the following documents:
  • 1471-2164-14-S3-S7-S1.xlsx, sheet 1
View BVdb publication page