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