Is IDS p.Val311= (c.933C>T) pathogenic?

IDS p.Val311= (c.933C>T) is classified Likely benign in IDS (ClinVar, Multiple submitters, 3 submitters; last evaluated 2025-12-03). Ultra-rare (popmax 0.0178%, eas); Associated with mucopolysaccharidosis type 2.

What condition is associated with IDS p.Val311= (c.933C>T)?

IDS p.Val311= (c.933C>T) is associated with mucopolysaccharidosis type 2 (ClinVar).

How common is IDS p.Val311= (c.933C>T) in the general population?

IDS p.Val311= (c.933C>T) is ultra-rare (popmax 0.0178%, eas) (gnomAD).

How is Mucopolysaccharidosis type 2 inherited?

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

IDS p.Val311=

c.933C>T · rs782608372 · VCV990715

Likely benign Multiple submitters

Classification

Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 3 submitters

gnomAD v4.1

Rare

ultra-rare (popmax 0.0178%, eas)

Conditions

mucopolysaccharidosis type 2

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 -2.8	GERP -3.2
Overall
CADD	0.186	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0178% East Asian · 6/33,755 alleles

Filtering AF 0.00766% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00527%

Overall 0.00116% 14/1,207,703 alleles · ultra-rare exomes 13/1,095,903 · genomes 1/111,800 · joint denominator

Ancestry group	Frequency	1 in
East Asiangrpmax	0.0178%	5,626
Remaining individualsnot grpmax-eligible	0.00421%	23,757
South Asian	0.00352%	28,395
Admixed American	0.00218%	45,783
European (non-Finnish)	0.000336%	297,725

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: IDS
Protein: p.Val311=
Coding: c.933C>T
MANE Select: NM_000202
dbSNP: rs782608372
Type: single nucleotide variant
Location: chrX:149490387 (GRCh38)
Structure: AlphaFold pLDDT 93.39 · 2 PDB
Residue 311: an α-helix

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

Disease context

mucopolysaccharidosis type 2 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Mucopolysaccharidosis type 2 (Orphanet):

Inheritance: X-linked recessive
Onset: Childhood
Prevalence: 1-9 / 1 000 000 (Europe)

Similar variants

IDS p.Val311Leu Conflicting classifications of pathogenicity ★ ⚠ same residue
IDS p.Val311Phe Uncertain significance ★ ⚠ same residue
IDS c.1006+1G>C Pathogenic ★★ same condition
IDS c.1006+1G>T Pathogenic ★★ same condition
IDS c.1007-133A>G Likely pathogenic ★★ same condition
IDS c.1007-1G>A Pathogenic ★★ same condition
IDS c.1007-2A>C Pathogenic/Likely pathogenic ★★ same condition
IDS c.1007-8T>G 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/ids-p-val311 (accessed [today's date]).

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