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CFH c.2845T>C ;(p.Y949H)
Variant ID: 1-196709811-T-C
NM_000186.3(
CFH
):c.2845T>C;(p.Y949H)
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: CFH: 2845T>C
PubMed Link:
25151476
Variant Present in the following documents:
12864_2013_6386_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page