Variant ID: 1-230818841-G-T

NM_007357.2(COG2):c.1167-479G>T

This variant was identified in 2 publications




Publications:


A Genome-Wide mQTL Analysis in Human Adipose Tissue Identifies Genetic Variants Associated with DNA Methylation, Gene Expression and Metabolic Traits.

Plos One
P Volkov, AH Olsson, L Gillberg, SW Jørgensen, C Brøns, KF Eriksson, L Groop, PA Jansson, E Nilsson, T Rönn, A Vaag, C Ling
Publication Date: 2016

Variant appearance in text: rs2479131
PubMed Link: 27322064
Variant Present in the following documents:
  • pone.0157776.s014.xlsx
View BVdb publication page



Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.

Nature
Publication Date: 2007-06-07

Variant appearance in text: rs2479131
PubMed Link: 17554300
Variant Present in the following documents:
  • NIHMS4894-supplement-S1.pdf
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000366668.3 c.1167-479G>T - intron_variant - 10/17
ENST00000366669.4 c.1167-479G>T - intron_variant - 10/17
ENST00000468893.2 c.*1025-479G>T - intron_variant,NMD_transcript_variant - 11/18
ENST00000494371.1 n.7503G>T - non_coding_transcript_exon_variant 10/10 -
ENST00000534989.1 c.990-479G>T - intron_variant - 10/17
ENST00000535166.1 c.819-479G>T - intron_variant - 11/18
ENST00000546013.1 c.234-479G>T - intron_variant - 2/9
NM_001145036.2 c.1167-479G>T - intron_variant - 10/17
NM_007357.3 c.1167-479G>T - intron_variant - 10/17