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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