Variant ID: 13-42875512-C-T

NM_016248.3(AKAP11):c.2630C>T;(p.Ala877Val)

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: AKAP11: Ala877Val
PMID: 20876667
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000025301.2 c.2630C>T p.Ala877Val missense_variant 8/13 -
NM_016248.4 c.2630C>T p.Ala877Val missense_variant 8/13 -