EGFR c.2734T>C ;(p.S912P)

Variant ID: 7-55266442-T-C

NM_005228.3(EGFR):c.2734T>C;(p.S912P)

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:

Missense Mutations in Exons 18-24 of EGFR in Hepatocellular Carcinoma Tissues.

Biomed Research International
Panvichian, Ravat R; Tantiwetrueangdet, Anchalee A; Sornmayura, Pattana P; Leelaudomlipi, Surasak S
Publication Date: 2015

Variant appearance in text: EGFR: 2734T>C; S912P
PubMed Link: 26436086
Variant Present in the following documents:
  • Main text
  • BMRI2015-171845.pdf
View BVdb publication page