Variant ID: 11-116943354-A-C

NM_025164.6(SIK3):c.273+25505T>G

This variant was identified in 1 publication




Publications:


Genome-wide significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review.

American Journal Of Epidemiology
OA Panagiotou, E Evangelou, JP Ioannidis
Publication Date: 2010-10-15

Variant appearance in text: rs1351452
PMID: 20876667
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000292055.4 c.99+25505T>G - intron_variant - 1/23
ENST00000375288.1 c.-1607+25505T>G - intron_variant - 1/22
ENST00000375300.1 c.273+25505T>G - intron_variant - 1/23
ENST00000415541.1 c.129+25505T>G - intron_variant,NMD_transcript_variant - 1/24
ENST00000434315.2 c.-329+25505T>G - intron_variant - 1/24
ENST00000445177.1 c.253+25505T>G - intron_variant - 1/24
ENST00000446921.2 c.273+25505T>G - intron_variant - 1/23
ENST00000485363.1 n.163+25505T>G - intron_variant,non_coding_transcript_variant - 1/4
ENST00000542607.1 c.99+25505T>G - intron_variant - 1/23
NM_001281748.3 c.-329+25505T>G - intron_variant - 1/24
NM_001281749.3 c.273+25505T>G - intron_variant - 1/23
NM_001366686.2 c.273+25505T>G - intron_variant - 1/24
NM_001366687.1 c.273+25505T>G - intron_variant - 1/4
NM_025164.6 c.273+25505T>G - intron_variant - 1/23
- - TF_binding_site_variant - -
- - TF_binding_site_variant - -
- - TF_binding_site_variant - -
- - TF_binding_site_variant - -
- - TF_binding_site_variant - -
- - TF_binding_site_variant - -