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RNF168 c.774T>C ;(p.S258=)
Variant ID: 3-196199632-A-G
NM_152617.3(
RNF168
):c.774T>C;(p.S258=)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
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UCSC Genome Browser
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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: RNF168: S258S
PubMed Link:
25151476
Variant Present in the following documents:
Main text
12864_2013_Article_6386.pdf
View BVdb publication page