EPHA2 c.2121G>A ;(p.K707=)

Variant ID: 1-16458763-C-T

NM_004431.3(EPHA2):c.2121G>A;(p.K707=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Confirming putative variants at ≤ 5% allele frequency using allele enrichment and Sanger sequencing.

Scientific Reports
Yan, Yan Helen YH; Chen, Sherry X SX; Cheng, Lauren Y LY; Rodriguez, Alyssa Y AY; Tang, Rui R; Cabrera, Karina K; Zhang, David Yu DY
Publication Date: 2021-06-02

Variant appearance in text: EPHA2: 2121G>A
PubMed Link: 34079006
Variant Present in the following documents:
  • 41598_2021_91142_MOESM2_ESM.xlsx, sheet 2
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: K707K
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