MCM5 p.Pro211=
c.633G>A · rs367908521 · VCV1624498
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
ultra-rare (popmax 0.099%, mid)
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
|---|---|---|
| Constraint at this position | ||
| Conservation | phyloP -15 | GERP -3.1 |
| Overall | ||
| CADD | 0.621 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.099%
Middle Eastern · 6/6,060 alleles
Filtering AF
0.043%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.0295%
Overall
0.00415%
67/1,614,180 alleles · ultra-rare
exomes 60/1,461,830 · genomes 7/152,350 · joint denominator
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Middle Easterngrpmax | 0.099% | 1,010 |
| Remaining individualsnot grpmax-eligible | 0.0048% | 20,834 |
| European (non-Finnish) | 0.00475% | 21,072 |
| East Asian | 0.00446% | 22,439 |
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
- MCM5
- Protein
- p.Pro211=
- Coding
- c.633G>A
- MANE Select
- NM_006739
- dbSNP
- rs367908521
- Type
- single nucleotide variant
- Location
- chr22:35408444 (GRCh38)
- Gene constraint
- LOEUF 0.753 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 78.57 · 27 PDB
Similar variants
- MCM5 p.Pro211Arg Uncertain significance ★ ⚠ same residue
- MCM5 p.Pro211Leu Uncertain significance ★ ⚠ same residue
- MCM5 p.Ala160Val Uncertain significance ★★ ⚠ same type
- MCM5 p.Ala327Val Uncertain significance ★★ ⚠ same type
- MCM5 p.Ala543Thr Uncertain significance ★★ ⚠ same type
- MCM5 p.Ala620Thr Uncertain significance ★★ ⚠ same type
- MCM5 p.Arg138His Uncertain significance ★★ ⚠ same type
- MCM5 p.Arg167Cys 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/mcm5-p-pro211 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown