AIMP2 p.Thr195=
c.585G>A · rs767064905 · VCV3029218
Likely benign
No assertion criteria
Classification
Likely benign
ClinVar
Review
No assertion criteria ☆☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 0.00898%, sas)
Conditions
1
AIMP2-related disorder
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 -6 | |
| Overall | ||
| CADD | 0.84 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.00898%
South Asian · 8/89,082 alleles
Filtering AF
0.00445%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.00318%
Overall
0.00113%
18/1,598,818 alleles · very rare
| Ancestry group | Frequency | 1 in |
|---|---|---|
| South Asiangrpmax | 0.00898% | 11,135 |
| African / African-American | 0.0027% | 37,035 |
| East Asian | 0.00223% | 44,786 |
| Admixed American | 0.00174% | 57,508 |
| Remaining individualsnot grpmax-eligible | 0.00162% | 61,772 |
| European (non-Finnish) | 0.000426% | 234,794 |
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
- AIMP2
- Protein
- p.Thr195=
- Coding
- c.585G>A
- MANE Select
- NM_006303
- dbSNP
- rs767064905
- Type
- single nucleotide variant
- Location
- chr7:6023313 (GRCh38)
- Gene constraint
- LOEUF 1.107 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 81.65 · 13 PDB
- Residue 195
- the 'interaction with tp53' region; a UniProt-annotated variant site (in hld17)
Disease context
AIMP2-related disorder
Similar variants
- AIMP2 p.Gly42= Likely benign same condition
- AIMP2 p.Ser160= Likely benign same condition
- PMS2 c.-2146C>A Benign ★★★ same type
- PMS2 c.-2559T>A Benign ★★★ same type
- PMS2 c.-323G>T Benign ★★★ same type
- AIMP2 p.Tyr35Ter Likely pathogenic ★★ same type
- AIMP2 p.Ala240Val Uncertain significance ★★ ⚠ same type
- AIMP2 p.Arg215Cys 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/aimp2-p-thr195 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown