EIF2B5 p.Asp613=
c.1839C>T · rs1713735121 · VCV2102388
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 0.00133%, afr)
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 -0.013 | GERP -3.4, phastCons 0.47 |
| Overall | ||
| CADD | 5.77 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.00133%
African / African-American · 1/75,058 alleles
Overall
6.84e-05%
1/1,461,880 alleles · very rare
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
- EIF2B5
- Protein
- p.Asp613=
- Coding
- c.1839C>T
- MANE Select
- NM_003907
- dbSNP
- rs1713735121
- Type
- single nucleotide variant
- Location
- chr3:184143535 (GRCh38)
- Gene constraint
- LOEUF 0.544 · pLI 0.16 (gnomAD)
- Structure
- AlphaFold pLDDT 79.35 · 37 PDB
- Residue 613
- the w2 domain
Similar variants
- EIF2B5 p.Asp613Asn Uncertain significance ⚠ same residue
- EIF2B5 p.Ala403Val Pathogenic/Likely pathogenic ★★ ⚠ same type
- EIF2B5 p.Arg113Cys Pathogenic/Likely pathogenic ★★ ⚠ same type
- EIF2B5 p.Arg113His Pathogenic ★★ ⚠ same type
- EIF2B5 p.Arg121Ter Pathogenic/Likely pathogenic ★★ same type
- EIF2B5 p.Arg136Cys Pathogenic/Likely pathogenic ★★ same type
- EIF2B5 p.Arg136His Pathogenic ★★ same type
- EIF2B5 p.Arg195Cys 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/eif2b5-p-asp613 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown