SEC16A c.1108G>A ;(p.G370R)

Variant ID: 9-139370960-C-T

NM_014866.1(SEC16A):c.1108G>A;(p.G370R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome resequencing and bioinformatic analysis of SNP containing candidate genes in the autoimmune vitiligo Smyth line chicken model.

Bmc Genomics
Jang, Hyeon-Min HM; Erf, Gisela F GF; Rowland, Kaylee C KC; Kong, Byung-Whi BW
Publication Date: 2014-08-23

Variant appearance in text: SEC16A: 1108G>A
PubMed Link: 25151476
Variant Present in the following documents:
  • Main text
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