CHTF18 c.2609G>C ;(p.G870A)

Variant ID: 16-846968-G-C

NM_022092.2(CHTF18):c.2609G>C;(p.G870A)

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: CHTF18: G870A
PubMed Link: 25151476
Variant Present in the following documents:
  • Main text
  • 12864_2013_Article_6386.pdf
View BVdb publication page