Variant ID: 11-116813979-A-C

NM_025164.6(SIK3):c.454+10781T>G

This variant was identified in 3 publications




Publications:


Effect of Interaction between Early Menarche and Genetic Polymorphisms on Triglyceride.

Oxidative Medicine And Cellular Longevity
HS Lee, S Leem, B Oh, T Park
Publication Date: 2019

Variant appearance in text: rs12292858
PubMed Link: 30931082
Variant Present in the following documents:
  • Main text
View BVdb publication page



Multiple susceptibility loci at chromosome 11q23.3 are associated with plasma triglyceride in East Asians.

Journal Of Lipid Research
B Gombojav, SJ Lee, M Kho, YM Song, K Lee, J Sung
Publication Date: 2016-02

Variant appearance in text: rs12292858
PubMed Link: 26634697
Variant Present in the following documents:
  • Main text
View BVdb publication page



On the analysis of a repeated measure design in genome-wide association analysis.

International Journal Of Environmental Research And Public Health
Y Lee, S Park, S Moon, J Lee, RC Elston, W Lee, S Won
Publication Date: 2014-11-28

Variant appearance in text: rs12292858
PubMed Link: 25464127
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000292055.4 c.280+10781T>G - intron_variant - 3/23
ENST00000375288.1 c.-1426+10781T>G - intron_variant - 3/22
ENST00000375300.1 c.454+10781T>G - intron_variant - 3/23
ENST00000413553.1 c.161+10781T>G - intron_variant - 2/12
ENST00000415541.1 c.434+6870T>G - intron_variant,NMD_transcript_variant - 4/24
ENST00000434315.2 c.-24+6870T>G - intron_variant - 4/24
ENST00000445177.1 c.434+10781T>G - intron_variant - 3/24
ENST00000446921.2 c.454+10781T>G - intron_variant - 3/23
ENST00000485363.1 n.344+10781T>G - intron_variant,non_coding_transcript_variant - 3/4
ENST00000497049.1 n.181+10781T>G - intron_variant,non_coding_transcript_variant - 2/5
ENST00000542607.1 c.280+10781T>G - intron_variant - 3/23
NM_001281748.3 c.-24+6870T>G - intron_variant - 4/24
NM_001281749.3 c.454+10781T>G - intron_variant - 3/23
NM_001366686.2 c.454+10781T>G - intron_variant - 3/24
NM_001366687.1 c.454+10781T>G - intron_variant - 3/4
NM_025164.6 c.454+10781T>G - intron_variant - 3/23