Bibliome.ai browser hg19
Search
About
Stats
FAQ
APOE c.526C>A ;(p.R176S)
Variant ID: 19-45412079-C-A
NM_000041.2(
APOE
):c.526C>A;(p.R176S)
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: Arg176Ser
PubMed Link:
28559539
Variant Present in the following documents:
Main text
41598_2017_Article_1737.pdf
View BVdb publication page