Variant #0000001427 (NC_000016.10:g.53763606T>C, NC_000016.10(NM_001080432.2):c.46-46534T>C (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.53763606T>C |
Published as |
- |
Reference |
Y D Apalasamy et al. (2012), dbSNP |
DB-ID |
FTO_000019 |
dbSNP ID |
rs6499643 |
Frequency |
50/158 |
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 International |
Created by |
Nuur Athirah Binti Mohd Daud |
Date created |
2020-12-23 12:26:18 +08:00 (CST) |
Date last edited |
2021-08-29 12:33:43 +08:00 (CST) |

Variant on transcripts
Screenings
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