Bibliome.ai browser hg19
Search
About
Stats
FAQ
ANGPTL4 c.201C>G ;(p.S67R)
Variant ID: 19-8429406-C-G
NM_139314.1(
ANGPTL4
):c.201C>G;(p.S67R)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Validation of Polygenic Risk Scores for Coronary Heart Disease in a Middle Eastern Cohort Using Whole Genome Sequencing.
Circulation. Genomic And Precision Medicine
Saad, Mohamad M; El-Menyar, Ayman A; Kunji, Khalid K; Ullah, Ehsan E; Al Suwaidi, Jassim J; Kullo, Iftikhar J IJ
Publication Date: 2022-10-12
Variant appearance in text: rs538554190
PubMed Link:
36252120
Variant Present in the following documents:
Main text
View BVdb publication page
GESPA: classifying nsSNPs to predict disease association.
Bmc Bioinformatics
Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J
Publication Date: 2015-07-25
Variant appearance in text: ANGPTL4: S67R
PubMed Link:
26206375
Variant Present in the following documents:
12859_2015_673_MOESM1_ESM.xls, sheet 2
View BVdb publication page
Identification of rare causal variants in sequence-based studies: methods and applications to VPS13B, a gene involved in Cohen syndrome and autism.
Plos Genetics
Ionita-Laza, Iuliana I; Capanu, Marinela M; De Rubeis, Silvia S; McCallum, Kenneth K; Buxbaum, Joseph D JD
Publication Date: 2014-12
Variant appearance in text: ANGPTL4: Ser67Arg
PubMed Link:
25502226
Variant Present in the following documents:
Main text
pgen.1004729.pdf
View BVdb publication page