Variant #0000931075 (NC_000019.9:g.46032414del, NM_001017989.2:c.445del (OPA3))
| Chromosome |
19 |
| 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.46032414del |
| DNA change (hg38) |
- |
| Published as |
OPA3(NM_001017989.2):c.445delC (p.L149Wfs*67), OPA3(NM_001017989.3):c.445delC (p.L149Wfs*67) |
| ISCN |
- |
| DB-ID |
OPA3_000011 See all 3 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_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2023-07-07 10:10:56 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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