Variant ID: 11-116752219-A-G

NM_025164.6(SIK3):c.866-4461T>C

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: rs7124741
PMID: 20876667
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000292055.4 c.692-4461T>C - intron_variant - 6/23
ENST00000375288.1 c.-1014-4461T>C - intron_variant - 6/22
ENST00000375300.1 c.866-4461T>C - intron_variant - 6/23
ENST00000413553.1 c.573-4461T>C - intron_variant - 5/12
ENST00000415541.1 c.*390-4461T>C - intron_variant,NMD_transcript_variant - 7/24
ENST00000434315.2 c.389-4461T>C - intron_variant - 7/24
ENST00000445177.1 c.846-4461T>C - intron_variant - 6/24
ENST00000446921.2 c.866-4461T>C - intron_variant - 6/23
ENST00000542607.1 c.692-4461T>C - intron_variant - 6/23
NM_001281748.3 c.389-4461T>C - intron_variant - 7/24
NM_001281749.3 c.866-4461T>C - intron_variant - 6/23
NM_001366686.2 c.866-4461T>C - intron_variant - 6/24
NM_025164.6 c.866-4461T>C - intron_variant - 6/23