EOGT p.His464=
c.1392C>T · rs762688739 · VCV762735
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
ultra-rare (popmax 0.01%, amr)
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 0.85 | GERP -0.57, phastCons 1 |
| Overall | ||
| CADD | 3.613 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.01%
Admixed American · 6/59,806 alleles
Filtering AF
0.0043%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.00296%
Overall
0.00112%
18/1,612,922 alleles · ultra-rare
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Admixed Americangrpmax | 0.01% | 9,968 |
| Remaining individualsnot grpmax-eligible | 0.0032% | 31,222 |
| European (non-Finnish) | 0.000848% | 117,959 |
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
- EOGT
- Protein
- p.His464=
- Coding
- c.1392C>T
- MANE Select
- NM_001278689
- dbSNP
- rs762688739
- Type
- single nucleotide variant
- Location
- chr3:68978378 (GRCh38)
- Gene constraint
- LOEUF 1.121 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 91.71
Similar variants
- EOGT p.His464Arg Uncertain significance ★ ⚠ same residue
- EOGT c.1335-1G>A Pathogenic/Likely pathogenic ★★ same type
- EOGT c.311+1G>T Pathogenic/Likely pathogenic ★★ same type
- EOGT c.621-2A>T Pathogenic/Likely pathogenic ★★ same type
- EOGT p.Arg149His Uncertain significance ★★ ⚠ same type
- EOGT p.Arg372Trp Uncertain significance ★★ ⚠ same type
- EOGT p.Arg377Trp Uncertain significance ★★ ⚠ same type
- EOGT p.Arg452His 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/eogt-p-his464 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown