TRAF3IP2 p.Pro335=
c.1005G>T · VCV3653632
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Absent
absent from gnomAD v4.1
Conditions
1
candidiasis, familial, 8
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 -2.4 | GERP -3.8 |
| Overall | ||
| CADD | 0.368 | 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
- TRAF3IP2
- Protein
- p.Pro335=
- Coding
- c.1005G>T
- MANE Select
- NM_147686
- Type
- single nucleotide variant
- Location
- chr6:111580214 (GRCh38)
- Gene constraint
- LOEUF 0.771 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 53.91 · 1 PDB
- Residue 335
- 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 p.Pro335Leu Uncertain significance ★ ⚠ 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-pro335 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown