RB1 c.1312T>G ;(p.C438G)

Variant ID: 13-48951150-T-G

NM_000321.2(RB1):c.1312T>G;(p.C438G)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome wide SNP comparative analysis between EGFR and KRAS mutated NSCLC and characterization of two models of oncogenic cooperation in non-small cell lung carcinoma.

Bmc Medical Genomics
Blons, Hélène H; Pallier, Karine K; Le Corre, Delphine D; Danel, Claire C; Tremblay-Gravel, Maxime M; Houdayer, Claude C; Fabre-Guillevin, Elizabeth E; Riquet, Marc M; Dessen, Philippe P; Laurent-Puig, Pierre P
Publication Date: 2008-06-12

Variant appearance in text: RB1: c438G
PubMed Link: 18549475
Variant Present in the following documents:
  • Main text
  • 1755-8794-1-25.pdf
View BVdb publication page