SEPTIN7 c.77A>G ;(p.N26S)

Variant ID: 7-35872418-A-G

NM_001788.5(SEPTIN7):c.77A>G;(p.N26S)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

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: SEPT7: N26S
PubMed Link: 25151476
Variant Present in the following documents:
  • Main text
View BVdb publication page