Variant ID: 5-33944889-G-A

NM_016180.3(SLC45A2):c.1457C>T;(p.Ala486Val)

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: MATP: Ala486Val
PMID: 20876667
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000296589.4 c.1457C>T p.Ala486Val missense_variant 7/7 -
ENST00000342059.3 c.1280C>T p.Ala427Val missense_variant 6/6 -
NM_016180.5 c.1457C>T p.Ala486Val missense_variant 7/7 -