EIF2B2 p.Ser262=
c.786C>T · rs773215545 · VCV3013060
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 -0.49 | GERP 0.94, phastCons 0.029 |
| Overall | ||
| CADD | 9.023 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Remaining individualsnot grpmax-eligible | 0.0048% | 20,837 |
| European (non-Finnish)grpmax | 8.47e-05% | 1,180,038 |
Remaining individuals shows a higher raw frequency than the grpmax group above it. gnomAD excludes bottlenecked groups — Finnish, Ashkenazi Jewish, Amish and “Remaining individuals” — from grpmax, because founder effects make their frequencies unrepresentative for filtering. The table is sorted by frequency, so an excluded group can sit above the grpmax row.
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
- EIF2B2
- Protein
- p.Ser262=
- Coding
- c.786C>T
- MANE Select
- NM_014239
- dbSNP
- rs773215545
- Type
- single nucleotide variant
- Location
- chr14:75006669 (GRCh38)
- Gene constraint
- LOEUF 1.25 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 86.82 · 38 PDB
Similar variants
- EIF2B2 c.285-1G>A Likely pathogenic ★★ same type
- EIF2B2 c.832-2A>G Likely pathogenic ★★ same type
- EIF2B2 p.Arg172Ter Pathogenic/Likely pathogenic ★★ same type
- EIF2B2 p.Arg183Ter Pathogenic/Likely pathogenic ★★ same type
- EIF2B2 p.Glu213Gly Pathogenic ★★ ⚠ same type
- EIF2B2 p.Glu304Ter Pathogenic/Likely pathogenic ★★ same type
- EIF2B2 p.Gly200Val Pathogenic/Likely pathogenic ★★ same type
- EIF2B2 p.Lys273Arg Pathogenic/Likely pathogenic ★★ ⚠ 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/eif2b2-p-ser262 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown