TOP3A p.Arg722=
c.2166C>T · rs150782687 · VCV2082644
Benign
Single submitter
Classification
Benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 2 submitters
gnomAD v4.1
Rare
rare (popmax 0.307%, afr)
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 -3.6 | GERP -3.4 |
| Overall | ||
| CADD | 3.579 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.307%
African / African-American · 220/71,704 alleles
Filtering AF
0.274%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.261%
Overall
0.0188%
285/1,513,488 alleles · rare
exomes 158/1,361,196 · genomes 127/152,292 · joint denominator
| Ancestry group | Frequency | 1 in |
|---|---|---|
| African / African-Americangrpmax | 0.307% | 326 |
| Admixed American | 0.0114% | 8,799 |
| Remaining individualsnot grpmax-eligible | 0.00689% | 14,515 |
| European (non-Finnish) | 0.00477% | 20,946 |
| Ashkenazi Jewishnot grpmax-eligible | 0.00429% | 23,320 |
| East Asian | 0.00228% | 43,856 |
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
- TOP3A
- Protein
- p.Arg722=
- Coding
- c.2166C>T
- MANE Select
- NM_004618
- dbSNP
- rs150782687
- Type
- single nucleotide variant
- Location
- chr17:18278336 (GRCh38)
- Gene constraint
- LOEUF 0.737 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 84.14 · 2 PDB
- Residue 722
- a UniProt-annotated variant site (in peob5)
Similar variants
- TOP3A p.Arg722His Uncertain significance ★★ ⚠ same residue
- TOP3A c.990+1G>T Likely pathogenic ★★ same type
- TOP3A p.Arg135Ter Pathogenic/Likely pathogenic ★★ same type
- TOP3A p.Arg177Ter Pathogenic/Likely pathogenic ★★ same type
- TOP3A p.Arg338Ter Pathogenic/Likely pathogenic ★★ same type
- TOP3A p.Ala622Thr Uncertain significance ★★ ⚠ same type
- TOP3A p.Ala642Val Uncertain significance ★★ ⚠ same type
- TOP3A p.Ala941Thr Uncertain significance ★★ ⚠ 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/top3a-p-arg722 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown