Variant #0000553758 (NC_000015.9:g.28326863del, NM_000275.2:c.163del (OCA2))
| Chromosome |
15 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.28326863del |
| DNA change (hg38) |
g.28081717del |
| Published as |
OCA2(NM_000275.2):c.163delG (p.(Ala55Leufs*47)), OCA2(NM_000275.2):c.163delG (p.A55Lfs*47), OCA2(NM_000275.3):c.163delG (p.A55Lfs*47) |
| ISCN |
- |
| DB-ID |
OCA2_000026 See all 5 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) |
Retrieve |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-07-08 13:22:38 +02:00 (CEST) |

Variant on transcripts
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