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ANGPTL4 c.1081G>A ;(p.G361S)
Variant ID: 19-8438630-G-A
NM_139314.1(
ANGPTL4
):c.1081G>A;(p.G361S)
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: G361S
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: Gly361Ser
PubMed Link:
25502226
Variant Present in the following documents:
Main text
pgen.1004729.pdf
View BVdb publication page