Variant ID: 16-89986133-T-A

NM_002386.3(MC1R):c.467T>A;(p.Val156Glu)

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: MC1R: Val156Glu
PMID: 20876667
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000540694.1 n.813T>A - non_coding_transcript_exon_variant 2/2 -
ENST00000555147.1 c.467T>A p.Val156Glu missense_variant 1/1 -
ENST00000555427.1 c.467T>A p.Val156Glu missense_variant 3/4 -
ENST00000556922.1 c.467T>A p.Val156Glu missense_variant 1/5 -
NM_002386.3 c.467T>A p.Val156Glu missense_variant 1/1 -