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ANGPTL4 c.229G>C ;(p.G77R)
Variant ID: 19-8429434-G-C
NM_139314.1(
ANGPTL4
):c.229G>C;(p.G77R)
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:
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: G77R
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: Gly77Arg
PubMed Link:
25502226
Variant Present in the following documents:
Main text
View BVdb publication page
Phylogenetics applied to genotype/phenotype association and selection analyses with sequence data from angptl4 in humans.
International Journal Of Molecular Sciences
Maxwell, Taylor J TJ; Bendall, Matthew L ML; Staples, Jeffrey J; Jarvis, Todd T; Crandall, Keith A KA
Publication Date: 2010-01-25
Variant appearance in text: ANGPTL4: G77R
PubMed Link:
20162021
Variant Present in the following documents:
Main text
ijms-11-00370.pdf
View BVdb publication page