CFB p.Arg150Gln
c.449_450delinsAG · VCV3622826
Uncertain significance
Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| Splicing | ||
| SpliceAI | — | not assessed · substitutions only |
|---|---|---|
| Constraint at this position | ||
| Conservation | phyloP 6.7 | GERP 1.7, phastCons 1 |
Variant & gene context
- Gene
- CFB
- Protein
- p.Arg150Gln
- Coding
- c.449_450delinsAG
- MANE Select
- NM_001710
- Type
- Indel
- Location
- chr6:31947157 (GRCh38)
- Gene constraint
- LOEUF 0.719 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 86.54 · 28 PDB
- Residue 150
- the sushi 2 domain
Similar variants
- CFB p.Arg150= Benign/Likely benign ★★ same residue
- CFB p.Arg150Ter Uncertain significance ★ same residue
- CFB c.1855+2_1855+3delinsAC Uncertain significance ★ same type
- CFB p.Arg32Ter Uncertain significance ★ same type
- CFB p.Glu243_Gly244delinsGlyVal Uncertain significance ★ same type
- CFB p.Lys357Ala 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/cfb-p-arg150gln (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown