Is SYN1 p.Ile369= (c.1107C>T) pathogenic?

SYN1 p.Ile369= (c.1107C>T) is classified Conflicting classifications of pathogenicity in SYN1 (ClinVar, Conflicting submitters, 10 submitters; last evaluated 2026-01-13). Rare (popmax 0.218%, nfe); Associated with epilepsy, X-linked 1, with variable learning disabilities and behavior disorders.

How common is SYN1 p.Ile369= (c.1107C>T) in the general population?

SYN1 p.Ile369= (c.1107C>T) is rare (popmax 0.218%, nfe) (gnomAD).

SYN1 p.Ile369=

Q: What condition is associated with SYN1 p.Ile369= (c.1107C>T)?

SYN1 p.Ile369= (c.1107C>T) is associated with epilepsy, X-linked 1, with variable learning disabilities and behavior disorders (ClinVar).

Q: How is X-linked epilepsy-learning disabilities-behavior disorders syndrome inherited?

Typically X-linked recessive (Orphanet). A genetic counselor can assess individual risk for a family.

c.1107C>T · rs150248483 · VCV96363

Conflicting classifications of pathogenicity Conflicting submitters

Classification

Conflicting classifications of pathogenicity

ClinVar

Review

Conflicting submitters ★☆☆☆

ClinVar · 10 submitters

gnomAD v4.1

Rare

rare (popmax 0.218%, nfe)

Conditions

epilepsy, X-linked 1, with variable learning disabilities and behavior disorders

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 2.6	phastCons 1
Overall
CADD	4.328	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.218% European (non-Finnish) · 1,946/891,638 alleles

Filtering AF 0.21% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.207%

Overall 0.167% 2,008/1,203,169 alleles · rare exomes 1,894/1,091,124 · genomes 114/112,045 · joint denominator

Ancestry group	Frequency	1 in
European (non-Finnish)grpmax	0.218%	458
Remaining individualsnot grpmax-eligible	0.0718%	1,392
African / African-American	0.028%	3,567
Admixed American	0.0222%	4,505
Finnishnot grpmax-eligible	0.00434%	23,066

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: SYN1
Protein: p.Ile369=
Coding: c.1107C>T
MANE Select: NM_006950
dbSNP: rs150248483
Type: single nucleotide variant
Location: chrX:47576182 (GRCh38)
Structure: AlphaFold pLDDT 69.86
Residue 369: the 'c; actin-binding and synaptic-vesicle binding' region

Full SYN1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

epilepsy, X-linked 1, with variable learning disabilities and behavior disorders — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For X-linked epilepsy-learning disabilities-behavior disorders syndrome (Orphanet):

Inheritance: X-linked recessive
Onset: Childhood

Similar variants

SYN1 c.528-2A>T Pathogenic/Likely pathogenic ★★ same condition
SYN1 c.838-2A>G Likely pathogenic ★★ same condition
SYN1 p.Arg234Ter Pathogenic ★★ same condition
SYN1 p.Arg420Gln Likely pathogenic ★★ ⚠ same condition
SYN1 p.Arg422Ter Pathogenic ★★ same condition
SYN1 p.Gln483Ter Pathogenic ★★ same condition
SYN1 p.Gln555Ter Pathogenic ★★ same condition
SYN1 p.Glu121Ter Pathogenic/Likely pathogenic ★★ 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/syn1-p-ile369 (accessed [today's date]).

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