Variant #0000002748 (NC_000013.10:g.77569212G>A, CLN5(NM_006493.2):c.335G>A)
| Individual ID |
00002748 |
| Chromosome |
13 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.77569212G>A |
| Reference |
Pineda-Trujillo et al. 2005 Neurology 64:740-742;Cregeen, pers comm |
| DB-ID |
CLN5_000008 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| 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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