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WAC p.Ser481Ter

c.1440dup · VCV4820587

Pathogenic Single submitter
Classification
Pathogenic
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
Consequence
nonsense (stop-gain)
predicted LoF
gnomAD v4.1
Rare
Conditions
1
Paediatric disorders

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Consequencenonsense (stop-gain)predicted loss-of-function in a haploinsufficient gene (ClinGen)
NMDpredictedpremature termination codon in exon 11 of 14
Splicing
SpliceAI—not assessed · substitutions only
Constraint at this position
ConservationphyloP 12GERP 1.5, phastCons 1

Predicted loss-of-function is descriptive, not an applied PVS1 code.

Variant & gene context

Gene
WAC
Protein
p.Ser481Ter
Coding
c.1440dup
MANE Select
NM_016628
Type
Duplication
Location
chr10:28614567 (GRCh38)
Gene constraint
LOEUF 0.248 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure
AlphaFold pLDDT 55.71
Residue 481
a UniProt-annotated variant site (found in a patient with severe intellectual disability; likely pathogenic); the 'disordered' region
Full WAC gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Paediatric disorders

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/wac-p-ser481ter (accessed [today's date]).

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