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FCRL4 c.*464G>A
Variant ID: 1-157544850-C-T
NM_031282.2(
FCRL4
):c.*464G>A
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:
Analysis of the association between Fc receptor family gene polymorphisms and ocular Behçet's disease in Han Chinese.
Scientific Reports
Zhang, Donglei D; Qin, Jieying J; Li, Lin L; Su, Guannan G; Huang, Guo G; Cao, Qingfeng Q; Kijlstra, Aize A; Yang, Peizeng P
Publication Date: 2018-03-19
Variant appearance in text: rs14335
PubMed Link:
29555961
Variant Present in the following documents:
Main text
41598_2018_Article_23222.pdf
View BVdb publication page
Human FcR polymorphism and disease.
Current Topics In Microbiology And Immunology
Li, Xinrui X; Gibson, Andrew W AW; Kimberly, Robert P RP
Publication Date: 2014
Variant appearance in text: rs14335
PubMed Link:
25116105
Variant Present in the following documents:
Main text
978-3-319-07911-0_Chapter_13.pdf
View BVdb publication page