TET3 p.Pro305=
c.915A>T · VCV4873031
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Absent
absent from gnomAD v4.1
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 0.4 | GERP -1.1, phastCons 0.69 |
| Overall | ||
| CADD | 6.45 | 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
- TET3
- Protein
- p.Pro305=
- Coding
- c.915A>T
- MANE Select
- NM_001287491
- Type
- single nucleotide variant
- Location
- chr2:74046832 (GRCh38)
- Gene constraint
- LOEUF 0.213 · pLI 1.00 (gnomAD)
- Structure
- AlphaFold pLDDT 52.49 · 2 PDB
Similar variants
- TET3 p.Pro305Leu Uncertain significance ★ ⚠ same residue
- TET3 p.Arg1034Ter Pathogenic/Likely pathogenic ★★ same type
- TET3 p.Arg1150Ter Pathogenic ★★ same type
- TET3 p.Arg911Gln Likely pathogenic ★★ same type
- TET3 p.Arg1054His Uncertain significance ★★ ⚠ same type
- TET3 p.Arg1688Cys Uncertain significance ★★ ⚠ same type
- TET3 p.Arg1744His Uncertain significance ★★ ⚠ same type
- TET3 p.Arg430Gly Uncertain significance ★★ ⚠ same type
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/tet3-p-pro305 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown