CD36 c.(?_-183
Pathogenic
Single submitter
Classification
Pathogenic
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
Conditions
1
platelet-type bleeding disorder 10
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type. |
Variant & gene context
- Gene
- CD36
- Coding
- c.(?_-183
- MANE Select
- NM_001001548 · reported on NM_001001547
- Type
- Deletion
- Gene constraint
- LOEUF 1.953 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
- Structure
- AlphaFold pLDDT 94.14 · 1 PDB
Similar variants
- CD36 p.Ile399fs Pathogenic/Likely pathogenic ★★ same condition
- CD36 p.Ile410_Ile413del Pathogenic/Likely pathogenic ★★ same condition
- CD36 p.Lys213fs Pathogenic/Likely pathogenic ★★ same condition
- CD36 p.Lys223fs Pathogenic/Likely pathogenic ★★ same condition
- CD36 c.818+1_818+9del Likely pathogenic ★ same condition
- CD36 p.Gln171fs Likely pathogenic ★ same condition
- CD36 p.Lys36fs Likely pathogenic ★ same condition
- CD36 p.Thr197fs Likely pathogenic ★ 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/cd36-c-minus-183 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown