TRAF3IP2 p.Pro370=
c.1110C>T · VCV4780323
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 2.6 | GERP 0.067, phastCons 1 |
| Overall | ||
| CADD | 6.656 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
| Ancestry group | Frequency | 1 in |
|---|---|---|
| African / African-Americangrpmax | 0.00535% | 18,697 |
| Remaining individualsnot grpmax-eligible | 0.0016% | 62,408 |
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
- TRAF3IP2
- Protein
- p.Pro370=
- Coding
- c.1110C>T
- MANE Select
- NM_147686
- Type
- single nucleotide variant
- Location
- chr6:111575734 (GRCh38)
- Gene constraint
- LOEUF 0.771 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 53.91 · 1 PDB
- Residue 370
- the 'disordered' region
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 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
- TRAF3IP2 p.Gly353Asp 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-pro370 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown