EPHA2 c.1638C>G ;(p.V546=)

Variant ID: 1-16461007-G-C

NM_004431.3(EPHA2):c.1638C>G;(p.V546=)

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:

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: V546V
PubMed Link: 29267365
Variant Present in the following documents:
  • Main text
  • pone.0189881.s004.xlsx, sheet 3
  • pone.0189881.pdf
  • pone.0189881.s004.xlsx, sheet 1
  • pone.0189881.s004.xlsx, sheet 2
View BVdb publication page