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.




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