Variant #0000002757 (NC_000013.10:g.77570221G>A, CLN5(NM_006493.2):c.671G>A)
| Individual ID |
00002757 |
| Chromosome |
13 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.77570221G>A |
| Reference |
Cregeen, pers comm;Xin et al 2010 Neurology 74:565-71 |
| DB-ID |
CLN5_000017 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
2.0E-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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