TONSL p.Ala1037=
c.3111C>T · rs142494135 · VCV1164478
Benign
Single submitter
Classification
Benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 2 submitters
gnomAD v4.1
Rare
low-frequency (popmax 2.56%, eas)
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 -1.4 | GERP -3.3 |
| Overall | ||
| CADD | 0.511 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
2.56%
East Asian · 1,103/43,084 alleles
Filtering AF
2.43%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 2.38%
Overall
0.198%
3,009/1,521,458 alleles · low-frequency
exomes 2,706/1,369,154 · genomes 303/152,304 · joint denominator
| Ancestry group | Frequency | 1 in |
|---|---|---|
| East Asiangrpmax | 2.56% | 39 |
| South Asian | 1.46% | 69 |
| Finnishnot grpmax-eligible | 0.997% | 100 |
| Remaining individualsnot grpmax-eligible | 0.187% | 535 |
| Middle Eastern | 0.0429% | 2,329 |
| Ashkenazi Jewishnot grpmax-eligible | 0.0208% | 4,804 |
| European (non-Finnish) | 0.00556% | 17,985 |
| African / African-American | 0.00277% | 36,114 |
| Admixed American | 0.00208% | 47,986 |
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
- TONSL
- Protein
- p.Ala1037=
- Coding
- c.3111C>T
- MANE Select
- NM_013432
- dbSNP
- rs142494135
- Type
- single nucleotide variant
- Location
- chr8:144434254 (GRCh38)
- Gene constraint
- LOEUF 1.024 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 76.06 · 3 PDB
- Residue 1037
- a UniProt-annotated variant site (in semdsp; disease phenotype includes immunologic and hematologic abnormalities); a UniProt-annotated variant site (in semdsp); a UniProt-annotated variant site (in semdsp; disease phenotype includes primary aphakia and absent pupils)
Similar variants
- TONSL c.1891-1G>C Pathogenic/Likely pathogenic ★★ same type
- TONSL p.Arg875Ter Pathogenic/Likely pathogenic ★★ same type
- TONSL p.Arg934Trp Pathogenic ★★ ⚠ same type
- TONSL p.Gln177Ter Pathogenic/Likely pathogenic ★★ same type
- TONSL p.Gln511Ter Pathogenic/Likely pathogenic ★★ same type
- TONSL p.Glu487Lys Pathogenic/Likely pathogenic ★★ ⚠ same type
- TONSL c.2775+5G>T Uncertain significance ★★ same type
- TONSL p.Ala1053Ser 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/tonsl-p-ala1037 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown