Variant #0000655409 (NC_000005.9:g.74014717T>A, NM_000521.3:c.1338T>A (HEXB))
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.74014717T>A |
| DNA change (hg38) |
g.74718892T>A |
| Published as |
HEXB(NM_000521.4):c.1338T>A (p.(Ser446=)), HEXB(NM_001292004.1):c.663T>A (p.S221=) |
| ISCN |
- |
| DB-ID |
HEXB_000043 See all 2 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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