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CD320 p.Arg151Cys

c.451C>T · rs769150463 · VCV1018004

Uncertain significance Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
AlphaMissense
likely pathogenic
0.5674 · ACMG-weighted
gnomAD v4.1
Rare
very rare (popmax 0.00112%, sas)
Missense predictors
2/2 damaging
AlphaMissense, SaProt · REVEL no call
Conditions
1
methylmalonic acidemia due to transcobalamin receptor defect

Computational evidence

Protein change
AlphaMissense0.5674likely pathogenic
REVEL0.638indeterminate
SaProtLLR -12.78damaging
⇒ AlphaMissense and SaProt both call this damaging; REVEL makes no call.
Splicing
SpliceAI—not assessed · no allele here is in the release
Constraint at this position
ConservationphyloP 3.3GERP 0.94, phastCons 1
Regional constrainto/e 1.03unconstrained · MANE · 5,824 bp · p 0.57 · regional, not allelic
Overall
CADD24.0PHRED · no single calibrated threshold — expert panels disagree

ClinVar classifies this uncertain; the computational predictors unanimously lean damaging — a triage signal, not a reclassification

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

Population frequency

gnomAD v4.1 · exomes + genomes
Grpmax group 0.00112% South Asian · 1/89,478 alleles
Overall 0.000125% 2/1,605,936 alleles · very rare exomes 2/1,453,562 · genomes 0/152,374 · joint denominator
Ancestry group Frequency 1 in
South Asiangrpmax 0.00112% 89,478
European (non-Finnish) 8.5e-05% 1,176,743

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.Arg151Cys
Coding
c.451C>T
MANE Select
NM_016579
dbSNP
rs769150463
Type
single nucleotide variant
Location
chr19:8303906 (GRCh38)
Gene constraint
LOEUF 1.488 · pLI <0.01 (gnomAD)
Structure
AlphaFold pLDDT 64.61 · 6 PDB
Residue 151
the ldl-receptor class a 2 domain
Full CD320 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

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-arg151cys (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown