CLMN p.Asp592=
c.1776C>T · rs144975674 · VCV787953
Benign
Multiple submitters
Classification
Benign
ClinVar
Review
Multiple submitters ★★☆☆
ClinVar · 3 submitters
gnomAD v4.1
Rare
low-frequency (popmax 2.07%, afr)
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 -10 | GERP -4.9 |
| Overall | ||
| CADD | 0.117 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
2.07%
African / African-American · 1,552/75,006 alleles
Filtering AF
1.98%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 1.95%
Overall
0.107%
1,723/1,614,120 alleles · low-frequency
exomes 823/1,461,884 · genomes 900/152,236 · joint denominator
| Ancestry group | Frequency | 1 in |
|---|---|---|
| African / African-Americangrpmax | 2.07% | 48 |
| Admixed American | 0.115% | 870 |
| Remaining individualsnot grpmax-eligible | 0.114% | 880 |
| Middle Eastern | 0.0165% | 6,062 |
| European (non-Finnish) | 0.00237% | 42,144 |
| East Asian | 0.00223% | 44,886 |
| South Asian | 0.0011% | 91,076 |
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
- CLMN
- Protein
- p.Asp592=
- Coding
- c.1776C>T
- MANE Select
- NM_024734
- dbSNP
- rs144975674
- Type
- single nucleotide variant
- Location
- chr14:95203573 (GRCh38)
- Gene constraint
- LOEUF 0.755 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 52.84
- Residue 592
- the 'disordered' region
Similar variants
- CLMN p.Asp592Glu Uncertain significance ★ ⚠ same residue
- CLMN c.2511+10C>T Benign ★★ same type
- CLMN c.886-4G>T Likely benign ★★ same type
- CLMN p.Glu276Lys Likely benign ★★ same type
- CLMN p.Glu357Lys Benign ★★ same type
- CLMN p.Glu771Ala Likely benign ★★ same type
- CLMN p.His518= Benign ★★ same type
- CLMN p.Ile900Phe 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/clmn-p-asp592 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown