ACTA1 p.Ile167fs
c.498_528del · rs2102735931 · VCV1323848
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| Consequence | frameshift | predicted loss-of-function |
|---|---|---|
| NMD | predicted | premature termination codon in exon 4 of 7 |
| Splicing | ||
| SpliceAI | — | not assessed · substitutions only |
| Constraint at this position | ||
| Conservation | phyloP 7.8 | GERP 2.6, phastCons 1 |
Predicted loss-of-function is descriptive, not an applied PVS1 code.
Population frequency
No gnomAD frequency available for this variant. This is missing data, not an absence: the variant may or may not be present in gnomAD. Rarity (ACMG PM2) and BA1/BS1 cannot be assessed for it.
Variant & gene context
- Gene
- ACTA1
- Protein
- p.Ile167fs
- Coding
- c.498_528del
- MANE Select
- NM_001100
- dbSNP
- rs2102735931
- Type
- Deletion
- Location
- chr1:229432358 (GRCh38)
- Gene constraint
- LOEUF 0.931 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 95.21 · 5 PDB
- Residue 167
- a β-strand
Similar variants
- ACTA1 p.Asp181fs Pathogenic ★★★ same type
- ACTA1 p.Glu363_Tyr364insTer Likely pathogenic ★★★ same type
- ACTA1 c.809-35del Benign ★★★ same type
- ACTA1 p.Ala146fs Pathogenic/Likely pathogenic ★★ same type
- ACTA1 p.Phe92del Pathogenic/Likely pathogenic ★★ same type
- ACTA1 p.Asn117fs Likely pathogenic ★ same type
- ACTA1 p.Asp313fs Likely pathogenic ★ same type
- ACTA1 p.Gln316fs Likely pathogenic ★ same type
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/acta1-p-ile167fs (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown