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FTO c.1008A>G ;(p.Q336=)
Variant ID: 16-53913788-A-G
NM_001080432.2(
FTO
):c.1008A>G;(p.Q336=)
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:
Prevalence of loss-of-function FTO mutations in lean and obese individuals.
Diabetes
Meyre, David D; Proulx, Karine K; Kawagoe-Takaki, Hiroko H; Vatin, Vincent V; Gutiérrez-Aguilar, Ruth R; Lyon, Debbie D; Ma, Marcella M; Choquet, Helene H; Horber, Fritz F; Van Hul, Wim W; Van Gaal, Luc L; Balkau, Beverley B; Visvikis-Siest, Sophie S; Pattou, François F; Farooqi, I Sadaf IS; Saudek, Vladimir V; O'Rahilly, Stephen S; Froguel, Philippe P; Sedgwick, Barbara B; Yeo, Giles S H GS
Publication Date: 2010-01
Variant appearance in text: FTO: Q336Q
PubMed Link:
19833892
Variant Present in the following documents:
Main text
View BVdb publication page