OPA1 p.Ala166fs
c.496del · VCV4965554
Likely pathogenic
Single submitter
Classification
Likely pathogenic
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
Consequence
frameshift
predicted LoF
gnomAD v4.1
Rare
Conditions
1
OPA1-related disorder
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| Consequence | frameshift | predicted loss-of-function in a LoF-intolerant gene |
|---|---|---|
| NMD | predicted | premature termination codon in exon 4 of 31 |
| Splicing | ||
| SpliceAI | — | not assessed · substitutions only |
| Constraint at this position | ||
| Conservation | phyloP 3.2 | GERP -3.2, phastCons 1 |
Predicted loss-of-function is descriptive, not an applied PVS1 code.
Variant & gene context
- Gene
- OPA1
- Protein
- p.Ala166fs
- Coding
- c.496del
- MANE Select
- NM_130837
- Type
- Deletion
- Location
- chr3:193617225 (GRCh38)
- Gene constraint
- LOEUF 0.503 · pLI 0.92 (gnomAD)
- Structure
- AlphaFold pLDDT 74.02 · 11 PDB
Disease context
OPA1-related disorder
Similar variants
- OPA1 c.1377_1377+4del Pathogenic/Likely pathogenic ★★ same condition
- OPA1 c.2873_2876del Pathogenic/Likely pathogenic ★★ same condition
- OPA1 p.Phe802fs Pathogenic ★★ same condition
- OPA1 p.Ser763fs Pathogenic ★★ same condition
- OPA1 p.Tyr113fs Pathogenic ★★ same condition
- OPA1 p.Val997fs Pathogenic/Likely pathogenic ★★ same condition
- OPA1 c.1036-2del Likely pathogenic ★ same condition
- OPA1 c.1931_1935+18del Likely pathogenic ★ same condition
Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →
Cite Sugi Variant
Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/opa1-p-ala166fs (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown