ZYX p.Pro210Ser
c.628C>T · VCV3990727
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
AlphaMissense
likely benign
0.0632 · ACMG-weighted
gnomAD v4.1
Absent
absent from gnomAD v4.1
Missense predictors
0/3 damaging
AlphaMissense, REVEL, SaProt
Computational evidence
| Protein change | ||
| AlphaMissense | 0.0632 | likely benign |
|---|---|---|
| REVEL | 0.038 | moderately benign-leaning |
| SaProt | LLR -6.42 | 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 -0.11 | GERP 2.2 |
| Regional constraint | o/e 1.00 | unconstrained · MANE · 9,107 bp · p 0.99 · regional, not allelic |
| Overall | ||
| CADD | 8.524 | PHRED · no single calibrated threshold — expert panels disagree |
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
- ZYX
- Protein
- p.Pro210Ser
- Coding
- c.628C>T
- MANE Select
- NM_003461
- Type
- single nucleotide variant
- Location
- chr7:143382927 (GRCh38)
- Gene constraint
- LOEUF 0.863 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 63.57
- Residue 210
- the 'disordered' region
Similar variants
- ZYX p.Ala400= Benign ★★ same type
- ZYX p.Thr459= Benign ★★ same type
- ZYX p.Thr480= Benign ★★ same type
- ZYX p.Ala107Glu Uncertain significance ★ ⚠ same type
- ZYX p.Ala216Gly Uncertain significance ★ ⚠ same type
- ZYX p.Ala317Val Uncertain significance ★ ⚠ same type
- ZYX p.Ala408Ser Uncertain significance ★ ⚠ same type
- ZYX p.Ala416Val Uncertain significance ★ ⚠ 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/zyx-p-pro210ser (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown