Send feedback

CD320 p.Gly112Ser

c.334G>A · rs948576208 · VCV848693

Uncertain significance Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
AlphaMissense
likely benign
0.1075 · ACMG-weighted
gnomAD v4.1
Rare
very rare (popmax 0.00764%, amr)
Missense predictors
0/3 damaging
AlphaMissense, REVEL, SaProt
Conditions
1
methylmalonic acidemia due to transcobalamin receptor defect

Computational evidence

Protein change
AlphaMissense0.1075likely benign
REVEL0.145moderately benign-leaning
SaProtLLR -6.44tolerated
⇒ AlphaMissense, REVEL and SaProt all call this tolerated.
Splicing
SpliceAIΔ0.54acceptor gain · deltas
PangolinΔ0.21gain · loss 0.00 · agrees with SpliceAI · independent
Constraint at this position
ConservationphyloP -0.2GERP -0.46
Regional constrainto/e 1.03unconstrained · MANE · 5,824 bp · p 0.57 · regional, not allelic
Overall
CADD14.73PHRED · 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

gnomAD v4.1 · exomes + genomes
Grpmax group 0.00764% Admixed American · 4/52,386 alleles
Filtering AF 0.00258% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0015%
Overall 0.000767% 12/1,565,034 alleles · very rare
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
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-gly112ser (accessed [today's date]).

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