TLR3 p.Arg64Ser
c.192A>T · VCV4734921
Uncertain significance
Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
AlphaMissense
ambiguous
0.3959 · ACMG-weighted
gnomAD v4.1
Absent
absent from gnomAD v4.1
Missense predictors
0/2 damaging
REVEL, SaProt · AlphaMissense indeterminate
Conditions
1
herpes simplex encephalitis, susceptibility to, 1
Computational evidence
| Protein change | ||
| AlphaMissense | 0.3959 | ambiguous |
|---|---|---|
| REVEL | 0.134 | moderately benign-leaning |
| SaProt | LLR -5.08 | tolerated |
| ⇒ REVEL and SaProt both call this tolerated; AlphaMissense is indeterminate. | ||
| Splicing | ||
| SpliceAI | Δ0.29 | donor loss, 26 bp away · masked 0 · deltas |
| Constraint at this position | ||
| Conservation | phyloP 4.1 | GERP 2, phastCons 1 |
| Regional constraint | o/e 0.98 | unconstrained · MANE · 5,926 bp · p 0.74 · regional, not allelic |
| Overall | ||
| CADD | 19.47 | PHRED · no single calibrated threshold — expert panels disagree |
AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.
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
- TLR3
- Protein
- p.Arg64Ser
- Coding
- c.192A>T
- MANE Select
- NM_003265
- Type
- single nucleotide variant
- Location
- chr4:186076811 (GRCh38)
- Gene constraint
- LOEUF 0.796 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 90.64 · 20 PDB
Similar variants
- TLR3 p.Arg64Gly Uncertain significance ★ ⚠ same residue
- TLR3 p.Ala185Val Uncertain significance ★★ ⚠ same condition
- TLR3 p.Ala549Thr Uncertain significance ★★ ⚠ same condition
- TLR3 p.Ala795Val Uncertain significance ★★ ⚠ same condition
- TLR3 p.Ala839Asp Uncertain significance ★★ ⚠ same condition
- TLR3 p.Arg331Gln Uncertain significance ★★ ⚠ same condition
- TLR3 p.Arg331Trp Uncertain significance ★★ ⚠ same condition
- TLR3 p.Arg809Lys 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/tlr3-p-arg64ser (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown