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TRAF3IP2 p.Pro292=

c.876G>A · rs746125245 · VCV2728282

Likely benign Multiple submitters
Classification
Likely benign
ClinVar
Review
Multiple submitters ★★☆☆
ClinVar · 2 submitters
gnomAD v4.1
Rare
ultra-rare (popmax 0.0104%, nfe)
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
ConservationphyloP -3.8GERP -3.8
Overall
CADD3.439PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes
Grpmax group 0.0104% European (non-Finnish) · 122/1,172,218 alleles
Filtering AF 0.0089% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00833%
Overall 0.00804% 128/1,591,404 alleles · ultra-rare
Ancestry group Frequency 1 in
European (non-Finnish)grpmax 0.0104% 9,608
Admixed American 0.00556% 17,989
Remaining individualsnot grpmax-eligible 0.00326% 30,672
South Asian 0.00114% 87,658

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.Pro292=
Coding
c.876G>A
MANE Select
NM_147686
dbSNP
rs746125245
Type
single nucleotide variant
Location
chr6:111580343 (GRCh38)
Gene constraint
LOEUF 0.771 · pLI <0.01 (gnomAD)
Structure
AlphaFold pLDDT 53.91 · 1 PDB
Full TRAF3IP2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

candidiasis, familial, 8 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Chronic mucocutaneous candidiasis (Orphanet):

Inheritance
Autosomal dominant, Autosomal recessive
Onset
Childhood, Infancy

Similar variants

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-pro292 (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown