APOE c.592C>T ;(p.R198C)

Variant ID: 19-45412145-C-T

NM_000041.2(APOE):c.592C>T;(p.R198C)

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:

Analyses of the mitochondrial mutations in the Chinese patients with sporadic Creutzfeldt-Jakob disease.

European Journal Of Human Genetics : Ejhg
Zhang, Jin J; Zhang, Zhi-Xia ZX; Du, Peng-Chen PC; Zhou, Wei W; Wu, Su-Dong SD; Wang, Qi-Ling QL; Chen, Cao C; Shi, Qi Q; Chen, Chen C; Gao, Chen C; Tian, Chan C; Dong, Xiao-Ping XP
Publication Date: 2015-01

Variant appearance in text: APOE: 592C>T
PubMed Link: 24667788
Variant Present in the following documents:
  • Main text
View BVdb publication page