EDAR p.Cys428Arg
c.1282T>C · rs2470612697 · VCV1714868
Computational evidence
| Protein change | ||
| AlphaMissense | 0.9965 | likely pathogenic ✓ concordant with ClinVar · top 3% in EDAR |
|---|---|---|
| REVEL | 0.783 | moderately pathogenic-leaning |
| SaProt | LLR -10.02 | damaging |
| ⇒ AlphaMissense, REVEL and SaProt all call this damaging. | ||
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
| Constraint at this position | ||
| Conservation | phyloP 11 | GERP 1.8, phastCons 1 |
| Regional constraint | o/e 0.89 | unconstrained · MANE · 34 kb · p 0.0061 · regional, not allelic |
| Overall | ||
| CADD | 28.4 | PHRED · no single calibrated threshold — expert panels disagree |
AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.
Population frequency
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
- EDAR
- Protein
- p.Cys428Arg
- Coding
- c.1282T>C
- MANE Select
- NM_022336
- dbSNP
- rs2470612697
- Type
- single nucleotide variant
- Location
- chr2:108896972 (GRCh38)
- Gene constraint
- LOEUF 0.927 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 67.01 · 1 PDB
- Residue 428
- the death domain
Disease context
autosomal recessive hypohidrotic ectodermal dysplasia — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatmentsAlso linked: ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant
For Hypohidrotic ectodermal dysplasia (Orphanet):
- Inheritance
- Autosomal dominant, Autosomal recessive, X-linked recessive
- Onset
- Infancy, Neonatal
- Prevalence
- 1-9 / 100 000 (Europe)
Similar variants
- EDAR p.Cys428Trp Conflicting classifications of pathogenicity ★ ⚠ same residue
- EDAR p.Cys428Ter Likely pathogenic same residue
- EDAR p.Ala26Val Pathogenic/Likely pathogenic ★★ ⚠ same condition
- EDAR p.Arg25Ter Pathogenic/Likely pathogenic ★★ same condition
- EDAR p.Arg358Ter Pathogenic ★★ same condition
- EDAR p.Arg420Gln Pathogenic/Likely pathogenic ★★ same condition
- EDAR p.Arg89His Pathogenic/Likely pathogenic ★★ ⚠ same condition
- EDAR p.Arg98Trp Pathogenic/Likely pathogenic ★★ 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/edar-p-cys428arg (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown