EPHA2 c.2192C>T ;(p.A731V)

Variant ID: 1-16458692-G-A

NM_004431.3(EPHA2):c.2192C>T;(p.A731V)

This variant was identified in 2 publications

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Study of Caspase 8 mutation in oral cancer and adjacent precancer tissues and implication in progression.

Plos One
Singh, Richa R; Das, Shreya S; Datta, Sila S; Mazumdar, Anjana A; Biswas, Nidhan K NK; Maitra, Arindam A; Majumder, Partha P PP; Ghose, Sandip S; Roy, Bidyut B
Publication Date: 2020

Variant appearance in text: EPHA2: A731V
PubMed Link: 32492030
Variant Present in the following documents:
  • pone.0233058.s001.xlsx, sheet 6
View BVdb publication page


Germ-line and somatic EPHA2 coding variants in lens aging and cataract.

Plos One
Bennett, Thomas M TM; M'Hamdi, Oussama O; Hejtmancik, J Fielding JF; Shiels, Alan A
Publication Date: 2017

Variant appearance in text: EPHA2: A731V
PubMed Link: 29267365
Variant Present in the following documents:
  • Main text
  • pone.0189881.s005.xlsx, sheet 2
  • pone.0189881.s005.xlsx, sheet 3
  • pone.0189881.pdf
  • pone.0189881.s005.xlsx, sheet 1
View BVdb publication page