CD320 p.Gly112Ser
c.334G>A · rs948576208 · VCV848693
Computational evidence
| Protein change | ||
| AlphaMissense | 0.1075 | likely benign |
|---|---|---|
| REVEL | 0.145 | moderately benign-leaning |
| SaProt | LLR -6.44 | tolerated |
| ⇒ AlphaMissense, REVEL and SaProt all call this tolerated. | ||
| Splicing | ||
| SpliceAI | Δ0.54 | acceptor gain · deltas |
| Pangolin | Δ0.21 | gain · loss 0.00 · agrees with SpliceAI · independent |
| Constraint at this position | ||
| Conservation | phyloP -0.2 | GERP -0.46 |
| Regional constraint | o/e 1.03 | unconstrained · MANE · 5,824 bp · p 0.57 · regional, not allelic |
| Overall | ||
| CADD | 14.73 | PHRED · no single calibrated threshold — expert panels disagree |
ClinVar classifies this uncertain; the computational predictors unanimously lean tolerated — a triage signal, not a reclassification
AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.
Population frequency
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Admixed Americangrpmax | 0.00764% | 13,096 |
| East Asian | 0.00238% | 41,962 |
| Remaining individualsnot grpmax-eligible | 0.00165% | 60,654 |
| South Asian | 0.00117% | 85,372 |
| European (non-Finnish) | 0.000433% | 230,904 |
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
- CD320
- Protein
- p.Gly112Ser
- Coding
- c.334G>A
- MANE Select
- NM_016579
- dbSNP
- rs948576208
- Type
- single nucleotide variant
- Location
- chr19:8304023 (GRCh38)
- Gene constraint
- LOEUF 1.488 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 64.61 · 6 PDB
Similar variants
- CD320 p.Arg129Leu Uncertain significance ★★ ⚠ same condition
- CD320 p.Arg138Ser Uncertain significance ★★ ⚠ same condition
- CD320 p.Arg254Gln Uncertain significance ★★ ⚠ same condition
- CD320 p.Arg258His Uncertain significance ★★ ⚠ same condition
- CD320 p.Asn170Ser Uncertain significance ★★ ⚠ same condition
- CD320 p.Asp143Asn Uncertain significance ★★ ⚠ same condition
- CD320 p.Asp160Asn Uncertain significance ★★ ⚠ same condition
- CD320 p.Gly166Val Uncertain significance ★★ ⚠ same condition
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/cd320-p-gly112ser (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown