Variant #0000002854 (NC_000008.10:g.1728661G>C, CLN8(NM_018941.3):c.789G>C)
| Individual ID |
00002854 |
| Chromosome |
8 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1728661G>C |
| Reference |
Ranta et al. 2004 Hum Mutat 23:300-305;Mole et al 2005 Neurogenetics 6:107-26 |
| DB-ID |
CLN8_000014 |
| 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
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