Bibliome.ai browser hg19
Search
About
Stats
FAQ
ATP6V0A2 c.757C>T ;(p.P253S)
Variant ID: 12-124220103-C-T
NM_012463.3(
ATP6V0A2
):c.757C>T;(p.P253S)
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: ATP6V0A2: 757C>T; P253S
PubMed Link:
25151476
Variant Present in the following documents:
Main text
View BVdb publication page