ATRIP p.Arg11Lys
c.32G>A · rs757688146 · VCV2071781
Computational evidence
| Protein change | ||
| AlphaMissense | 0.1185 | likely benign |
|---|---|---|
| REVEL | 0.01 | strongly benign-leaning |
| SaProt | LLR -10.71 | damaging |
| ⇒ SaProt calls this damaging; AlphaMissense and REVEL do not. | ||
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
| Constraint at this position | ||
| Conservation | phyloP 4.4 | GERP -1.7, phastCons 1 |
| Regional constraint | o/e 0.95 | unconstrained · MANE · 19 kb · p 0.089 · regional, not allelic |
| Overall | ||
| CADD | 17.19 | PHRED · no single calibrated threshold — expert panels disagree |
AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.
Population frequency
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Finnishnot grpmax-eligible | 0.125% | 801 |
| European (non-Finnish)grpmax | 0.0119% | 8,375 |
| Remaining individualsnot grpmax-eligible | 0.00954% | 10,484 |
| Admixed American | 0.00921% | 10,856 |
| African / African-American | 0.0015% | 66,596 |
Finnish shows a higher raw frequency than the grpmax group above it. gnomAD excludes bottlenecked groups — Finnish, Ashkenazi Jewish, Amish and “Remaining individuals” — from grpmax, because founder effects make their frequencies unrepresentative for filtering. The table is sorted by frequency, so an excluded group can sit above the grpmax row.
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
- ATRIP
- Protein
- p.Arg11Lys
- Coding
- c.32G>A
- MANE Select
- NM_130384
- dbSNP
- rs757688146
- Type
- single nucleotide variant
- Location
- chr3:48446877 (GRCh38)
- Gene constraint
- LOEUF 0.707 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 70.10 · 24 PDB
- Residue 11
- the 'disordered' region
Similar variants
- ATRIP p.Arg11Thr Uncertain significance ★★ ⚠ same residue
- TREX1 p.Met11Arg Uncertain significance ★ same residue
- TREX1 p.Met11Thr Uncertain significance ★ ⚠ same residue
- ATRIP p.Arg11= Likely benign ★ same residue
- TREX1 p.Arg114His Pathogenic/Likely pathogenic ★★ ⚠ same type
- TREX1 p.Arg164Ter Pathogenic/Likely pathogenic ★★ same type
- TREX1 p.Asp18Asn Pathogenic ★★ same type
- TREX1 p.Asp200His 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/atrip-p-arg11lys (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown