TRAF3 p.Ser275=
c.825C>T · rs758246898 · VCV2888041
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 8.48e-05%, nfe)
Conditions
1
herpes simplex encephalitis, susceptibility to, 3
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 0.36 | GERP 2, phastCons 0.42 |
| Overall | ||
| CADD | 10.08 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
8.48e-05%
European (non-Finnish) · 1/1,179,212 alleles
Overall
6.2e-05%
1/1,612,016 alleles · very rare
exomes 1/1,460,200 · genomes 0/151,816 · joint denominator
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
- TRAF3
- Protein
- p.Ser275=
- Coding
- c.825C>T
- MANE Select
- NM_145725
- dbSNP
- rs758246898
- Type
- single nucleotide variant
- Location
- chr14:102897266 (GRCh38)
- Gene constraint
- LOEUF 0.321 · pLI 1.00 (gnomAD)
- Structure
- AlphaFold pLDDT 88.26 · 10 PDB
- Residue 275
- a UniProt-annotated variant site (in imd132b; likely pathogenic; decreased traf3 mrna and protein levels and absence of a truncated traf3 protein in patient cells)
Similar variants
- TRAF3 p.Ser275Phe Uncertain significance ★ ⚠ same residue
- TRAF3 p.Trp344Ter Pathogenic ★★ same condition
- TRAF3 p.Ala188Val Uncertain significance ★★ ⚠ same condition
- TRAF3 p.Ala371Thr Uncertain significance ★★ ⚠ same condition
- TRAF3 p.Ala371Val Uncertain significance ★★ ⚠ same condition
- TRAF3 p.Ala78Val Uncertain significance ★★ ⚠ same condition
- TRAF3 p.Ala90Val Uncertain significance ★★ ⚠ same condition
- TRAF3 p.Arg25Cys 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/traf3-p-ser275 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown