Send feedback

APTX p.Gly240=

c.720G>A · rs2489448574 · VCV3025174

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/SpliceAI carries the signal.
Splicing
SpliceAIΔ0.23donor gain · deltas
Constraint at this position
ConservationphyloP -0.81GERP -0.19
Overall
CADD5.609PHRED · 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
APTX
Protein
p.Gly240=
Coding
c.720G>A
MANE Select
NM_001195248
dbSNP
rs2489448574
Type
single nucleotide variant
Location
chr9:32984681 (GRCh38)
Gene constraint
LOEUF 0.973 · pLI <0.01 (gnomAD)
Structure
AlphaFold pLDDT 81.52 · 11 PDB
Residue 240
the hit domain; an α-helix
Full APTX 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/aptx-p-gly240 (accessed [today's date]).

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