LDLR p.Val853Asp
c.2558T>A · VCV3537738
Uncertain significance
Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
AlphaMissense
likely benign
0.0912 · ACMG-weighted
gnomAD v4.1
Absent
absent from gnomAD v4.1
Missense predictors
1/3 damaging
AlphaMissense, REVEL, SaProt
Conditions
1
Cardiovascular phenotype
Computational evidence
| Protein change | ||
| AlphaMissense | 0.0912 | likely benign |
|---|---|---|
| REVEL | 0.903 | moderately pathogenic-leaning |
| SaProt | LLR -7.78 | tolerated |
| ⇒ REVEL calls this damaging; AlphaMissense and SaProt do not. | ||
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
| Constraint at this position | ||
| Conservation | phyloP 7.7 | GERP 1.4, phastCons 1 |
| Regional constraint | o/e 1.00 | unconstrained · MANE · 42 kb · p 0.91 · regional, not allelic |
| Overall | ||
| CADD | 29.3 | PHRED · no single calibrated threshold — expert panels disagree |
AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.
Population frequency
gnomAD v4.1 · exomes + genomes
Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.
Variant & gene context
- Gene
- LDLR
- Protein
- p.Val853Asp
- Coding
- c.2558T>A
- MANE Select
- NM_000527
- Type
- single nucleotide variant
- Location
- chr19:11131291 (GRCh38)
- Gene constraint
- LOEUF 1.091 · pLI <0.01 · ClinGen HI 3/3 (gnomAD)
- Structure
- AlphaFold pLDDT 75.81 · 36 PDB
- Residue 853
- the 'required for mylip-triggered down-regulation of ldlr' region
Similar variants
- LDLR p.Val853= Likely benign ★ same residue
- LDLR p.Val853Leu Uncertain significance ★★ ⚠ same residue
- LDLR c.1061-1G>C Pathogenic/Likely pathogenic ★★ same condition
- LDLR c.1186+1G>T Pathogenic ★★ same condition
- LDLR c.1186+2T>G Pathogenic/Likely pathogenic ★★ same condition
- LDLR c.1586+1G>A Pathogenic/Likely pathogenic ★★ same condition
- LDLR c.1587-1G>A Pathogenic/Likely pathogenic ★★ same condition
- LDLR c.1587-2A>G Pathogenic/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/ldlr-p-val853asp (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown