Send feedback

ACAN p.Pro110=

c.330G>C · rs373654303 · VCV2888098

Likely benign Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Absent
absent from gnomAD v4.1

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI<0.2all four deltas below 0.2 · G>T here scores Δ0.22 · evaluated, not missing
Constraint at this position
ConservationphyloP -12GERP -3.5
Overall
CADD0.078PHRED · no single calibrated threshold — expert panels disagree

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
ACAN
Protein
p.Pro110=
Coding
c.330G>C
MANE Select
NM_001369268
dbSNP
rs373654303
Type
single nucleotide variant
Location
chr15:88838922 (GRCh38)
Gene constraint
LOEUF 0.377 · pLI 1.00 (gnomAD)
Structure
AlphaFold pLDDT 53.32 · 4 PDB
Residue 110
a disulfide bond; a turn; the ig-like v-type domain; the 'g1-a' region
Full ACAN 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/acan-p-pro110 (accessed [today's date]).

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