C2CD2 p.Val429=
c.1287C>T · rs77424551 · VCV777621
Benign
Single submitter
Classification
Benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
rare (popmax 0.949%, afr)
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| Splicing | ||
| SpliceAI | <0.2 | all four deltas below 0.2 · G>T here scores Δ0.21 · evaluated, not missing |
|---|---|---|
| Constraint at this position | ||
| Conservation | phyloP -2.1 | GERP -4.2 |
| Overall | ||
| CADD | 0.617 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.949%
African / African-American · 712/75,002 alleles
Filtering AF
0.892%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.868%
Overall
0.0469%
757/1,613,990 alleles · rare
| Ancestry group | Frequency | 1 in |
|---|---|---|
| African / African-Americangrpmax | 0.949% | 105 |
| Remaining individualsnot grpmax-eligible | 0.0304% | 3,289 |
| Admixed American | 0.02% | 5,001 |
| Middle Eastern | 0.0167% | 6,006 |
| East Asian | 0.00223% | 44,882 |
| South Asian | 0.0022% | 45,538 |
| European (non-Finnish) | 0.000847% | 117,997 |
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
- C2CD2
- Protein
- p.Val429=
- Coding
- c.1287C>T
- MANE Select
- NM_015500
- dbSNP
- rs77424551
- Type
- single nucleotide variant
- Location
- chr21:41907023 (GRCh38)
- Gene constraint
- LOEUF 0.924 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 62.52
Similar variants
- C2CD2 p.Pro104= Benign ★★ same type
- C2CD2 p.Ala123Val Uncertain significance ★ ⚠ same type
- C2CD2 p.Ala136Gly Uncertain significance ★ ⚠ same type
- C2CD2 p.Ala146Val Uncertain significance ★ ⚠ same type
- C2CD2 p.Ala189Thr Uncertain significance ★ ⚠ same type
- C2CD2 p.Ala207Val Uncertain significance ★ ⚠ same type
- C2CD2 p.Ala345Val Uncertain significance ★ ⚠ same type
- C2CD2 p.Ala466Thr 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/c2cd2-p-val429 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown