ANGPTL4 c.667G>C ;(p.G223R)

Variant ID: 19-8435945-G-C

NM_139314.1(ANGPTL4):c.667G>C;(p.G223R)

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:

Beyond Rare-Variant Association Testing: Pinpointing Rare Causal Variants in Case-Control Sequencing Study.

Scientific Reports
Lin, Wan-Yu WY
Publication Date: 2016-02-23

Variant appearance in text: ANGPTL4: G223R
PubMed Link: 26903168
Variant Present in the following documents:
  • Main text
  • srep21824.pdf
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: Gly223Arg
PubMed Link: 25502226
Variant Present in the following documents:
  • Main text
  • pgen.1004729.pdf
View BVdb publication page