HBA2 p.Pro115Arg
c.344C>G · rs267607269 · VCV3061293
Uncertain significance
Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 2 submitters
gnomAD v4.1
Absent
absent from gnomAD v4.1
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| REVEL | 0.468 | indeterminate |
|---|---|---|
| Splicing | ||
| SpliceAI | <0.2 | no splice effect predicted · four deltas, not one · how we know |
| Constraint at this position | ||
| Conservation | phyloP 0.29 | |
| Regional constraint | o/e 0.80 | unconstrained · MANE · 125 bp · p 0.14 · regional, not allelic |
| Overall | ||
| CADD | 17.59 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.
Variant & gene context
- Gene
- HBA2
- Protein
- p.Pro115Arg
- Coding
- c.344C>G
- MANE Select
- NM_000517
- dbSNP
- rs267607269
- Type
- single nucleotide variant
- Location
- chr16:173515 (GRCh38)
- Gene constraint
- LOEUF 1.915 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
- Structure
- AlphaFold pLDDT 98.04 · 348 PDB
- Residue 115
- a UniProt-annotated variant site (in nouakchott); a UniProt-annotated variant site (in chiapas); a UniProt-annotated variant site (in melusine); a turn; the globin domain
Similar variants
- HBA2 p.Pro115Leu Conflicting classifications of pathogenicity ★ same residue
- HBA2 p.Pro115Ser Uncertain significance ★ same residue
- HBA2 p.Cys105Arg Likely pathogenic ★★★ same type
- HBA2 p.Leu126Arg Likely pathogenic ★★★ same type
- HBA2 c.*98T>C Uncertain significance ★★★ same type
- HBA2 c.95+27C>T Benign ★★★ same type
- HBA2 c.-24C>G Benign ★★★ same type
- HBA2 c.*107A>G Benign ★★★ 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/hba2-p-pro115arg (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown