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APOB c.12669G>A ;(p.E4223=)
Variant ID: 2-21225625-C-T
NM_000384.2(
APOB
):c.12669G>A;(p.E4223=)
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:
Apolipoprotein B Gene Polymorphisms and Dyslipidemia in HIV Infected Adult Zimbabweans.
The Open Aids Journal
Kodogo, Vitaris V; Zhou, Danai Tavonga DT; Oektedalen, Olav O; Duri, Kerina K; Stray-Pedersen, Babill B; Gomo, Exnevia E
Publication Date: 2016
Variant appearance in text: APOB: 12669G>A
PubMed Link:
27790293
Variant Present in the following documents:
TOAIDJ-10-190.pdf
View BVdb publication page
Role of the APOB Gene Polymorphism (c.12669G>A, p. Gln4154Lys) in Coronary Artery Disease in the Indian Punjabi Population.
Balkan Journal Of Medical Genetics : Bjmg
Sharma, R R; Mahajan, M M; Singh, B B; Singh, G G; Singh, P P
Publication Date: 2011-12
Variant appearance in text: APOB: 12669G>A
PubMed Link:
24052710
Variant Present in the following documents:
Main text
bjmg-14-02-35.pdf
View BVdb publication page