Variant #0000002989 (NC_000015.10:g.34919C>G, NM_000520.5:c.1395C>G (HEXA))
Individual ID |
00000742 |
Chromosome |
15 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.34919C>G |
Published as |
- |
Reference |
L Y Chan et al.(2011) |
DB-ID |
HEXA_000002 |
dbSNP ID |
rs201604102 |
Frequency |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Nur Aisyah Athirah |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Nur Aisyah Athirah |
Date created |
2021-06-29 15:02:47 +08:00 (CST) |
Date last edited |
2021-09-09 15:08:45 +08:00 (CST) |

Variant on transcripts
Screenings
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