ACTG1 p.Arg177=
c.531T>C · rs143851458 · VCV44149
Benign/Likely benign
Multiple submitters
Classification
Benign/Likely benign
ClinVar
Review
Multiple submitters ★★☆☆
ClinVar · 8 submitters
gnomAD v4.1
Rare
rare (popmax 0.247%, mid)
Conditions
2
autosomal dominant nonsyndromic hearing loss 20
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
|---|---|---|
| Constraint at this position | ||
| Conservation | phyloP 1.8 | GERP 0.96, phastCons 1 |
| Overall | ||
| CADD | 12.73 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.247%
Middle Eastern · 15/6,062 alleles
Filtering AF
0.183%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.18%
Overall
0.151%
2,442/1,613,908 alleles · rare
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Middle Easterngrpmax | 0.247% | 404 |
| European (non-Finnish) | 0.19% | 528 |
| Remaining individualsnot grpmax-eligible | 0.142% | 702 |
| Admixed American | 0.11% | 910 |
| African / African-American | 0.0293% | 3,412 |
| Finnishnot grpmax-eligible | 0.0157% | 6,372 |
| Ashkenazi Jewishnot grpmax-eligible | 0.00338% | 29,608 |
| East Asian | 0.00223% | 44,880 |
| South Asian | 0.0011% | 91,090 |
Rarity supports pathogenicity (ACMG PM2); frequency above a disease-specific BA1/BS1 threshold argues against it. A variant frequent in one ancestry group can be near-absent in others, so a single global figure can mislead.
Variant & gene context
- Gene
- ACTG1
- Protein
- p.Arg177=
- Coding
- c.531T>C
- MANE Select
- NM_001614
- dbSNP
- rs143851458
- Type
- single nucleotide variant
- Location
- chr17:81511459 (GRCh38)
- Gene constraint
- LOEUF 0.617 · pLI 0.46 (gnomAD)
- Structure
- AlphaFold pLDDT 95.44 · 11 PDB
- Residue 177
- a β-strand
Similar variants
- ACTG1 p.Ala135Val Pathogenic/Likely pathogenic ★★ same condition
- ACTG1 p.Ala204Gly Likely pathogenic ★★ same condition
- ACTG1 p.Arg183Gln Pathogenic/Likely pathogenic ★★ same condition
- ACTG1 p.Arg183Trp Pathogenic/Likely pathogenic ★★ same condition
- ACTG1 p.Arg206Gln Pathogenic/Likely pathogenic ★★ same condition
- ACTG1 p.Arg210Cys Pathogenic ★★ same condition
- ACTG1 p.Arg254Trp Pathogenic/Likely pathogenic ★★ same condition
- ACTG1 p.Arg335His Pathogenic/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/actg1-p-arg177 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown