Variant #0000001136 (NC_000001.10:g.43395276_43395287del12, SLC2A1(NM_006516.2):c.844_855del12)
| Individual ID |
00001136 |
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.43395276_43395287del12 |
| Reference |
Weber YG1, Storch A, Wuttke TV, Brockmann K, Kempfle J, Maljevic S, Margari L, Kamm C, Schneider SA, Huber SM, Pekrun A, Roebling R, Seebohm G, Koka S, Lang C,(2008) |
| DB-ID |
SLC2A1_000015 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Y Yang |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Y Yang |

Variant on transcripts
Screenings
|