DAB2IP p.Pro920Leu
c.2759C>T · rs765361316 · VCV545131
Computational evidence
| Protein change | ||
| AlphaMissense | 0.3678 | ambiguous |
|---|---|---|
| REVEL | 0.153 | moderately benign-leaning |
| SaProt | LLR -7.73 | tolerated |
| ⇒ REVEL and SaProt both call this tolerated; AlphaMissense makes no call. | ||
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
| Constraint at this position | ||
| Conservation | phyloP 7.2 | GERP 2.3, phastCons 1 |
| Regional constraint | o/e 0.91 | unconstrained · MANE · 9,835 bp · p 0.021 · regional, not allelic |
| Overall | ||
| CADD | 24.8 | PHRED · no single calibrated threshold — expert panels disagree |
AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.
Population frequency
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Ashkenazi Jewishnot grpmax-eligible | 0.367% | 272 |
| Remaining individualsnot grpmax-eligible | 0.0254% | 3,943 |
| European (non-Finnish)grpmax | 0.00255% | 39,189 |
Ashkenazi Jewish 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
- DAB2IP
- Protein
- p.Pro920Leu
- Coding
- c.2759C>T
- MANE Select
- NM_001395010
- dbSNP
- rs765361316
- Type
- single nucleotide variant
- Location
- chr9:121773287 (GRCh38)
- Gene constraint
- LOEUF 0.407 · pLI 1.00 (gnomAD)
- Structure
- AlphaFold pLDDT 65.74
- Residue 920
- the 'disordered' region; the 'necessary for interaction with akt1' region
Similar variants
- DAB2IP p.Ala816Thr Benign ★★ same type
- DAB2IP p.Arg199= Benign ★★ same type
- DAB2IP p.Arg966His Benign ★★ same type
- DAB2IP p.Asp97= Benign/Likely benign ★★ same type
- DAB2IP p.Lys284= Benign ★★ same type
- DAB2IP p.Pro126= Likely benign ★★ same type
- DAB2IP p.Ser460Leu Benign ★★ ⚠ same type
- DAB2IP p.Ser68= Likely benign ★★ 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/dab2ip-p-pro920leu (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown