STAT5B p.Pro267Ala
c.799C>G · rs760893128 · VCV252678
Computational evidence
| Protein change | ||
| AlphaMissense | 0.093 | likely benign |
|---|---|---|
| REVEL | 0.517 | indeterminate |
| SaProt | LLR -9.31 | tolerated |
| ⇒ AlphaMissense and SaProt both call this tolerated; REVEL is indeterminate. | ||
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
| Constraint at this position | ||
| Conservation | phyloP 8.8 | GERP 1.8, phastCons 1 |
| Regional constraint | o/e 0.09 | constrained · MANE · 549 bp · p 1.7e-11 · regional, not allelic |
| Overall | ||
| CADD | 26.6 | PHRED · no single calibrated threshold — expert panels disagree |
ClinVar classifies this uncertain; the computational predictors unanimously lean tolerated — a triage signal, not a reclassification
AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.
Population frequency
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Finnishnot grpmax-eligible | 1.55% | 65 |
| South Asiangrpmax | 0.128% | 779 |
| Ashkenazi Jewishnot grpmax-eligible | 0.0937% | 1,068 |
| Admixed American | 0.0518% | 1,931 |
| East Asian | 0.0373% | 2,682 |
| Remaining individualsnot grpmax-eligible | 0.0282% | 3,551 |
| Middle Eastern | 0.0249% | 4,016 |
| European (non-Finnish) | 0.0187% | 5,337 |
| African / African-American | 0.0142% | 7,060 |
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
- STAT5B
- Protein
- p.Pro267Ala
- Coding
- c.799C>G
- MANE Select
- NM_012448
- dbSNP
- rs760893128
- Type
- single nucleotide variant
- Location
- chr17:42219346 (GRCh38)
- Gene constraint
- LOEUF 0.277 · pLI 1.00 (gnomAD)
- Structure
- AlphaFold pLDDT 85.90 · 2 PDB
- Residue 267
- the 'required for interaction with nmi' region
Similar variants
- STAT5B p.Pro267Ser Uncertain significance ★★ ⚠ same residue
- STAT5B c.1906+1G>A Likely pathogenic ★★ same type
- STAT5B p.Ala20Glu Uncertain significance ★★ ⚠ same type
- STAT5B p.Ala20Val Uncertain significance ★★ ⚠ same type
- STAT5B p.Ala213Gly Uncertain significance ★★ ⚠ same type
- STAT5B p.Ala213Ser Uncertain significance ★★ ⚠ same type
- STAT5B p.Ala723Thr Uncertain significance ★★ ⚠ same type
- STAT5B p.Ala785Thr 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/stat5b-p-pro267ala (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown