Variant ID: 16-28568678-C-T

NM_138414.3(SGF29):c.-16+3260C>T

This variant was identified in 4 publications




Publications:


Characterizing gene-gene interactions in a statistical epistasis network of twelve candidate genes for obesity.

Biodata Mining
R De, T Hu, JH Moore, D Gilbert-Diamond
Publication Date: 2015

Variant appearance in text: rs151320
PubMed Link: 26715945
Variant Present in the following documents:
  • 13040_2015_77_MOESM3_ESM.xlsx
  • 13040_2015_77_MOESM8_ESM.xlsx
View BVdb publication page



Genome-wide meta-analysis for severe diabetic retinopathy.

Human Molecular Genetics
MA Grassi, A Tikhomirov, S Ramalingam, JE Below, NJ Cox, DL Nicolae
Publication Date: 2011-06-15

Variant appearance in text: rs151320
PubMed Link: 21441570
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic control of individual differences in gene-specific methylation in human brain.

American Journal Of Human Genetics
D Zhang, L Cheng, JA Badner, C Chen, Q Chen, W Luo, DW Craig, M Redman, ES Gershon, C Liu
Publication Date: 2010-03-12

Variant appearance in text: rs151320
PubMed Link: 20215007
Variant Present in the following documents:
  • mmc6.xls
View BVdb publication page



Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.

Nature Genetics
JD Cooper, DJ Smyth, AM Smiles, V Plagnol, NM Walker, JE Allen, K Downes, JC Barrett, BC Healy, JC Mychaleckyj, JH Warram, JA Todd
Publication Date: 2008-12

Variant appearance in text: rs151320
PubMed Link: 18978792
Variant Present in the following documents:
  • NIHMS2312-supplement-Supplementary_.pdf
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000317058.3 c.-16+3260C>T - intron_variant - 1/9
ENST00000564682.1 n.183+3260C>T - intron_variant,non_coding_transcript_variant - 1/2
ENST00000567564.1 c.-16+3260C>T - intron_variant,NMD_transcript_variant - 1/7
ENST00000569581.1 n.178+3260C>T - intron_variant,non_coding_transcript_variant - 1/4
NM_138414.3 c.-16+3260C>T - intron_variant - 1/9