CCDC112 p.Thr186=
c.558A>G · rs146955785 · VCV788985
Benign
Single submitter
Classification
Benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
rare (popmax 0.404%, 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 1.3 | GERP 0.76, phastCons 1 |
| Overall | ||
| CADD | 8.644 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.404%
African / African-American · 299/74,010 alleles
Filtering AF
0.366%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.352%
Overall
0.0201%
320/1,595,484 alleles · rare
| Ancestry group | Frequency | 1 in |
|---|---|---|
| African / African-Americangrpmax | 0.404% | 248 |
| Remaining individualsnot grpmax-eligible | 0.0194% | 5,145 |
| Middle Eastern | 0.0167% | 5,982 |
| Admixed American | 0.00523% | 19,104 |
| South Asian | 0.00113% | 88,578 |
| European (non-Finnish) | 0.000342% | 292,457 |
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
- CCDC112
- Protein
- p.Thr186=
- Coding
- c.558A>G
- MANE Select
- NM_001040440
- dbSNP
- rs146955785
- Type
- single nucleotide variant
- Location
- chr5:115275576 (GRCh38)
- Gene constraint
- LOEUF 0.875 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 82.18
Similar variants
- CCDC112 p.Ala165Val Uncertain significance ★ ⚠ same type
- CCDC112 p.Ala299Ser Uncertain significance ★ ⚠ same type
- CCDC112 p.Ala434Pro Uncertain significance ★ ⚠ same type
- CCDC112 p.Ala68Pro Uncertain significance ★ same type
- CCDC112 p.Arg391Cys Uncertain significance ★ ⚠ same type
- CCDC112 p.Arg391His Uncertain significance ★ ⚠ same type
- CCDC112 p.Arg391Leu Uncertain significance ★ ⚠ same type
- CCDC112 p.Arg393Leu 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/ccdc112-p-thr186 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown