APOE c.882G>T ;(p.W294C)

Variant ID: 19-45412435-G-T

NM_000041.2(APOE):c.882G>T;(p.W294C)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Apolipoprotein E (APOE) Haplotypes in Healthy Subjects from Worldwide Macroareas: A Population Genetics Perspective for Cardiovascular Disease, Neurodegeneration, and Dementia.

Current Issues In Molecular Biology
Abondio, Paolo P; Bruno, Francesco F; Luiselli, Donata D
Publication Date: 2023-03-31

Variant appearance in text: rs557715042
PubMed Link: 37185708
Variant Present in the following documents:
  • Main text
  • cimb-45-00184.pdf
View BVdb publication page



Global genetic diversity of human apolipoproteins and effects on cardiovascular disease risk.

Journal Of Lipid Research
Zhou, Yitian Y; Mägi, Reedik R; Milani, Lili L; Lauschke, Volker M VM
Publication Date: 2018-10

Variant appearance in text: rs557715042
PubMed Link: 30076208
Variant Present in the following documents:
  • 10.1194_P086710_jlr.P086710-4.xlsx, sheet 3
View BVdb publication page



In silico analyses of deleterious missense SNPs of human apolipoprotein E3.

Scientific Reports
Pires, Allan S AS; Porto, William F WF; Franco, Octavio L OL; Alencar, Sérgio A SA
Publication Date: 2017-05-30

Variant appearance in text: APOE: Trp294Cys; rs557715042
PubMed Link: 28559539
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_1737.pdf
View BVdb publication page