Variant #0000002799 (NC_000015.9:g.68504037_68504039delGAT, CLN6(NM_017882.2):c.460_462delATC)
| Individual ID |
00002799 |
| Chromosome |
15 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.68504037_68504039delGAT |
| Reference |
Wheeler et al. 2002 Am J Hum Genet 70: 537-542;Teixeira et al. 2003 Hum Mut 21: 502-508;Creegan pers comm |
| DB-ID |
CLN6_000024 |
| 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
|