Variant #0000342773 (NC_000003.11:g.193332592_193332609del, OPA1(NM_015560.2):c.113_130del)
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.193332592_193332609del |
DNA change (hg38) |
g.193614803_193614820del |
Published as |
OPA1:NM_130837.2:c.113_130del (Arg38_Ser43del) |
ISCN |
- |
DB-ID |
OPA1_000082 See all 10 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland; Variant no longer found in the VKGL dataset for this center. |
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 |

Variant on transcripts
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