Variant #0000002572 (NC_000011.9:g.1780799G>A, CTSD(NM_001909.4):c.299C>T)
| Individual ID |
00002572 |
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1780799G>A |
| Reference |
Fritchie et al 2008. Acta Neuropathol 117: 201-208 |
| DB-ID |
CTSD_000001 |
| 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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