ITGA3 p.Ile570Val
c.1708A>G · VCV3286714
Computational evidence
| Protein change | ||
| AlphaMissense | 0.2054 | likely benign |
|---|---|---|
| REVEL | 0.073 | moderately benign-leaning |
| SaProt | LLR -7.64 | tolerated |
| ⇒ AlphaMissense, REVEL and SaProt all call this tolerated. | ||
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
| Constraint at this position | ||
| Conservation | phyloP 7.9 | GERP 1.9, phastCons 1 |
| Regional constraint | o/e 0.84 | unconstrained · MANE · 14 kb · p 6.1e-06 · regional, not allelic |
| Overall | ||
| CADD | 22.7 | PHRED · no single calibrated threshold — expert panels disagree |
ClinVar classifies this uncertain; the computational predictors unanimously lean tolerated — a triage signal, not a reclassification
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
- ITGA3
- Protein
- p.Ile570Val
- Coding
- c.1708A>G
- MANE Select
- NM_002204
- Type
- single nucleotide variant
- Location
- chr17:50076359 (GRCh38)
- Gene constraint
- LOEUF 0.69 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 83.88
Disease context
epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatmentsFor Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome (Orphanet):
- Inheritance
- Autosomal recessive
- Onset
- Infancy, Neonatal
Similar variants
- ITGA3 c.2070+1G>A Pathogenic ★★ same condition
- ITGA3 p.Arg274Gln Likely pathogenic ★★ ⚠ same condition
- ITGA3 p.Arg875Ter Likely pathogenic ★★ same condition
- ITGA3 c.*48G>A Uncertain significance ★★ same condition
- ITGA3 c.*96G>A Uncertain significance ★★ same condition
- ITGA3 p.Ala1026Val Uncertain significance ★★ ⚠ same condition
- ITGA3 p.Ala1035Val Uncertain significance ★★ ⚠ same condition
- ITGA3 p.Arg156Trp Uncertain significance ★★ ⚠ 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/itga3-p-ile570val (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown