APOE c.40G>A ;(p.A14T)

Variant ID: 19-45409921-G-A

NM_000041.2(APOE):c.40G>A;(p.A14T)

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:

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: Ala14Thr
PubMed Link: 28559539
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_1737.pdf
View BVdb publication page