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EDA p.Ser305Asn

c.914G>A · rs2020227357 · VCV1044137

Uncertain significance Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
AlphaMissense
likely pathogenic
0.9964 · ACMG-weighted
gnomAD v4.1
Absent
absent from gnomAD v4.1
Missense predictors
3/3 damaging
AlphaMissense, REVEL, SaProt
Conditions
1
X-linked hypohidrotic ectodermal dysplasia

Computational evidence

Protein change
AlphaMissense0.9964likely pathogenic · top 7% in EDA
REVEL0.846moderately pathogenic-leaning
SaProtLLR -11.44damaging
⇒ AlphaMissense, REVEL and SaProt all call this damaging.
Splicing
SpliceAIΔ0.20donor gain · deltas
PangolinΔ0.20gain · loss 0.07 · agrees with SpliceAI · independent
Constraint at this position
ConservationphyloP 12GERP 4.8, phastCons 1
Regional constrainto/e 0.62unconstrained · MANE · 419 kb · p 2e-10 · regional, not allelic
Overall
CADD32.0PHRED · no single calibrated threshold — expert panels disagree

ClinVar classifies this uncertain; the computational predictors unanimously lean damaging — a triage signal, not a reclassification

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

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
EDA
Protein
p.Ser305Asn
Coding
c.914G>A
MANE Select
NM_001399
dbSNP
rs2020227357
Type
single nucleotide variant
Location
chrX:70033518 (GRCh38)
Structure
AlphaFold pLDDT 70.59 · 3 PDB
Residue 305
a β-strand; the thd domain
Full EDA gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

X-linked hypohidrotic ectodermal dysplasia — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Hypohidrotic ectodermal dysplasia (Orphanet):

Inheritance
Autosomal dominant, Autosomal recessive, X-linked recessive
Onset
Infancy, Neonatal
Prevalence
1-9 / 100 000 (Europe)

Similar variants

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/eda-p-ser305asn (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown