Variant ID: 15-28483811-C-T

NM_004667.5(HERC2):c.3685G>A;(p.Asp1229Asn)

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: HERC2: Asp1229Asn
PMID: 20876667
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000261609.7 c.3685G>A p.Asp1229Asn missense_variant 24/93 -
NM_004667.5 c.3685G>A p.Asp1229Asn missense_variant 24/93 -