Variant #0000002749 (NC_000013.10:g.77569212G>C, CLN5(NM_006493.2):c.335G>C)
| Individual ID |
00002749 |
| 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>C |
| Reference |
Bessa et al. 2006 Mol Genet Mab 89:245-253 |
| DB-ID |
CLN5_000009 |
| 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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