Variant #0000929634 (NC_000010.10:g.100380410G>A, NM_021828.4:c.1154C>T (HPSE2))
| Chromosome |
10 |
| 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.100380410G>A |
| DNA change (hg38) |
- |
| Published as |
HPSE2(NM_021828.4):c.1154C>T (p.T385I) |
| ISCN |
- |
| DB-ID |
HPSE2_000021 |
| 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) |
0.00065 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2023-07-07 10:10:56 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
|