Variant #0000001431 (NC_000016.10:g.53799693T>A, FTO(NM_001080432.2):c.46-10447T>A)

Individual ID 00000296
Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.53799693T>A
Published as -
Reference Y D Apalasamy et al. (2012), dbSNP
DB-ID FTO_000023
dbSNP ID rs7204609
Frequency 70/158
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
FTO NM_001080432.2 +/. - c.46-10447T>A - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000311 DNA ? FTO 30 Nuur Athirah Binti Mohd Daud