Is CLN3 p.Ser151Asn (c.452G>A) pathogenic?

CLN3 p.Ser151Asn (c.452G>A) is classified Uncertain significance in CLN3 (ClinVar, Single submitter, 1 submitter; last evaluated 2022-10-26). AlphaMissense: likely pathogenic (0.6047); Absent from gnomAD v4.1; Associated with Inborn genetic diseases.

What condition is associated with CLN3 p.Ser151Asn (c.452G>A)?

CLN3 p.Ser151Asn (c.452G>A) is associated with Inborn genetic diseases (ClinVar).

How common is CLN3 p.Ser151Asn (c.452G>A) in the general population?

CLN3 p.Ser151Asn (c.452G>A) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about CLN3 p.Ser151Asn (c.452G>A)?

AlphaMissense predicts likely pathogenic (score 0.6047) — an in-silico prediction, not a clinical call.

CLN3 p.Ser151Asn

c.452G>A · rs2506491530 · VCV2319517

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely pathogenic

0.6047 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

2/2 damaging

AlphaMissense, SaProt · REVEL no call

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.6047	likely pathogenic
REVEL	0.373	indeterminate
SaProt	LLR -10.16	damaging
⇒ 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
Conservation	phyloP 7.6	GERP 1.7, phastCons 1
Regional constraint	o/e 0.93	unconstrained · MANE · 14 kb · p 0.08 · regional, not allelic
Overall
CADD	26.2	PHRED · 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

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: CLN3
Protein: p.Ser151Asn
Coding: c.452G>A
MANE Select: NM_001042432
dbSNP: rs2506491530
Type: single nucleotide variant
Location: chr16:28487464 (GRCh38)
Gene constraint: LOEUF 1.022 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Structure: AlphaFold pLDDT 81.81

Full CLN3 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Inborn genetic diseases — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

CLN3 p.Ser151Cys Uncertain significance ★ ⚠ same residue
CLN3 c.1056+1G>T Likely pathogenic ★★ same condition
CLN3 p.Ala59Thr Pathogenic/Likely pathogenic ★★ same condition
CLN3 p.Arg89Ter Pathogenic/Likely pathogenic ★★ same condition
CLN3 p.Val330Ile Pathogenic/Likely pathogenic ★★ ⚠ same condition
CLN3 c.-2C>G Uncertain significance ★★ same condition
CLN3 p.Ala103Val Uncertain significance ★★ ⚠ same condition
CLN3 p.Ala248Thr Uncertain significance ★★ ⚠ same condition

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/cln3-p-ser151asn (accessed [today's date]).

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