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CEP192 c.3938G>C ;(p.C1313S)
Variant ID: 18-13056527-G-C
NM_032142.3(
CEP192
):c.3938G>C;(p.C1313S)
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: CEP192: C1313S
PubMed Link:
25151476
Variant Present in the following documents:
Main text
12864_2013_Article_6386.pdf
12864_2013_6386_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page