Is SIM1 p.Gln483= (c.1449G>A) pathogenic?

SIM1 p.Gln483= (c.1449G>A) is classified Likely benign in SIM1 (ClinVar, No assertion criteria, 1 submitter; last evaluated 2024-03-15). Very rare (popmax 0.00891%, eas); Associated with SIM1-related disorder.

What condition is associated with SIM1 p.Gln483= (c.1449G>A)?

SIM1 p.Gln483= (c.1449G>A) is associated with SIM1-related disorder (ClinVar).

How common is SIM1 p.Gln483= (c.1449G>A) in the general population?

SIM1 p.Gln483= (c.1449G>A) is very rare (popmax 0.00891%, eas) (gnomAD).

SIM1 p.Gln483=

c.1449G>A · VCV3351424

Likely benign No assertion criteria

Classification

Likely benign

ClinVar

Review

No assertion criteria ☆☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 0.00891%, eas)

Conditions

SIM1-related disorder

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	<0.2	no splice effect predicted · four deltas, not one · how we know
Constraint at this position
Conservation	phyloP 1.4	GERP -0.74, phastCons 1
Overall
CADD	8.639	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00891% East Asian · 4/44,884 alleles

Filtering AF 0.00298% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0018%

Overall 0.000681% 11/1,614,136 alleles · very rare exomes 11/1,461,770 · genomes 0/152,366 · joint denominator

Ancestry group	Frequency	1 in
East Asiangrpmax	0.00891%	11,221
South Asian	0.0022%	45,541
Remaining individualsnot grpmax-eligible	0.0016%	62,508
European (non-Finnish)	0.000339%	294,986

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: SIM1
Protein: p.Gln483=
Coding: c.1449G>A
MANE Select: NM_005068
Type: single nucleotide variant
Location: chr6:100393608 (GRCh38)
Gene constraint: LOEUF 0.332 · pLI 1.00 · ClinGen HI 0/3 (gnomAD)
Structure: AlphaFold pLDDT 60.70
Residue 483: the single-minded c-terminal domain

Full SIM1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

SIM1-related disorder

Similar variants

SIM1 p.Gln483Arg Uncertain significance ⚠ same residue
SIM1 p.Arg374Trp Uncertain significance ★★ ⚠ same condition
SIM1 p.Ser199Cys Uncertain significance ★★ same condition
SIM1 p.Gly480Ter Likely pathogenic ★ same condition
SIM1 c.-468+6T>A Uncertain significance ★ same condition
SIM1 p.Ala484Ser Uncertain significance ★ ⚠ same condition
SIM1 p.Asn608Asp Uncertain significance ★ ⚠ same condition
SIM1 p.Lys287Arg 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/sim1-p-gln483 (accessed [today's date]).

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