Variant #0000001422 (NC_000016.10:g.53810667G>A, NC_000016.10(NM_001080432.2):c.123+450G>A (FTO))

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.53810667G>A
Published as -
Reference Y D Apalasamy et al. (2012), dbSNP
DB-ID FTO_000014
dbSNP ID rs17218700
Frequency 30/158
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
Date created 2020-12-22 16:49:07 +08:00 (CST)
Date last edited 2021-08-29 14:17:28 +08:00 (CST)
Options




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.123+450G>A - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000311 DNA ? FTO 30 Nuur Athirah Binti Mohd Daud