TRAF3IP2 p.Pro533Ser
c.1597C>T · rs2536087647 · VCV1896854
Computational evidence
| Protein change | ||
| AlphaMissense | 0.9917 | likely pathogenic · top 5% in TRAF3IP2 |
|---|---|---|
| REVEL | 0.519 | indeterminate |
| SaProt | LLR -10.20 | damaging |
| ⇒ AlphaMissense and SaProt both call this damaging; REVEL is indeterminate. | ||
| Splicing | ||
| SpliceAI | <0.2 | no splice effect predicted · four deltas, not one · how we know |
| Constraint at this position | ||
| Conservation | phyloP 12 | GERP 2.9, phastCons 1 |
| Regional constraint | o/e 0.62 | unconstrained · MANE · 14 kb · p 3.2e-08 · regional, not allelic |
| Overall | ||
| CADD | 28.1 | PHRED · no single calibrated threshold — expert panels disagree |
ClinVar classifies this uncertain; the computational predictors unanimously lean damaging — a triage signal, not a reclassification
AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.
⚠ Isoform check: AlphaMissense numbered on a different transcript (AM P542S vs ClinVar P533S) — verify the residue.
Population frequency
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
- TRAF3IP2
- Protein
- p.Pro533Ser
- Coding
- c.1597C>T
- MANE Select
- NM_147686
- dbSNP
- rs2536087647
- Type
- single nucleotide variant
- Location
- chr6:111559506 (GRCh38)
- Gene constraint
- LOEUF 0.771 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 53.91 · 1 PDB
- Residue 542 UniProt numbering
- the sefir domain
Disease context
candidiasis, familial, 8 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatmentsFor Chronic mucocutaneous candidiasis (Orphanet):
- Inheritance
- Autosomal dominant, Autosomal recessive
- Onset
- Childhood, Infancy
Similar variants
- TRAF3IP2 p.Pro533= Likely benign ★ same residue
- TRAF3IP2 c.1201+1G>C Likely pathogenic ★★ same condition
- TRAF3IP2 p.Ala328Thr Uncertain significance ★★ ⚠ same condition
- TRAF3IP2 p.Ala36Val Uncertain significance ★★ ⚠ same condition
- TRAF3IP2 p.Ala473Thr Uncertain significance ★★ ⚠ same condition
- TRAF3IP2 p.Asn45Lys Uncertain significance ★★ ⚠ same condition
- TRAF3IP2 p.Gln18His Uncertain significance ★★ ⚠ same condition
- TRAF3IP2 p.Glu479Lys Uncertain significance ★★ ⚠ same condition
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/traf3ip2-p-pro533ser (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown