ARID2 p.Ala1437=
c.4311G>A · rs138606745 · VCV748918
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
ultra-rare (popmax 0.0983%, amr)
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 6.7 | GERP 0.91, phastCons 1 |
| Overall | ||
| CADD | 12.1 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.0983%
Admixed American · 59/60,020 alleles
Filtering AF
0.0782%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.0709%
Overall
0.0106%
171/1,614,064 alleles · ultra-rare
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Admixed Americangrpmax | 0.0983% | 1,017 |
| African / African-American | 0.048% | 2,083 |
| Remaining individualsnot grpmax-eligible | 0.0288% | 3,472 |
| European (non-Finnish) | 0.00441% | 22,692 |
| Ashkenazi Jewishnot grpmax-eligible | 0.00338% | 29,606 |
| South Asian | 0.00329% | 30,360 |
| Finnishnot grpmax-eligible | 0.00312% | 32,005 |
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
- ARID2
- Protein
- p.Ala1437=
- Coding
- c.4311G>A
- MANE Select
- NM_152641
- dbSNP
- rs138606745
- Type
- single nucleotide variant
- Location
- chr12:45852434 (GRCh38)
- Gene constraint
- LOEUF 0.224 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
- Structure
- AlphaFold pLDDT 52.30 · 2 PDB
- Residue 1437
- a UniProt-annotated variant site (in css6)
Similar variants
- ARID2 p.Arg1272Ter Pathogenic ★★ same type
- ARID2 p.Arg1677Ter Pathogenic/Likely pathogenic ★★ same type
- ARID2 p.Arg1754Ter Pathogenic ★★ same type
- ARID2 p.Arg1769Ter Pathogenic ★★ same type
- ARID2 p.Arg274Ter Pathogenic/Likely pathogenic ★★ same type
- ARID2 p.Gln920Ter Pathogenic ★★ same type
- ARID2 p.Ala1335Glu Uncertain significance ★★ ⚠ same type
- ARID2 p.Arg1679Gln 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/arid2-p-ala1437 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown