Is CASK p.Val112= (c.336G>A) pathogenic?

CASK p.Val112= (c.336G>A) is classified Benign in CASK (ClinVar, Single submitter, 1 submitter; last evaluated 2024-04-08). Very rare (popmax 0.00351%, afr); Associated with Intellectual disability, CASK-related, X-linked.

What condition is associated with CASK p.Val112= (c.336G>A)?

CASK p.Val112= (c.336G>A) is associated with Intellectual disability, CASK-related, X-linked (ClinVar).

How common is CASK p.Val112= (c.336G>A) in the general population?

CASK p.Val112= (c.336G>A) is very rare (popmax 0.00351%, afr) (gnomAD).

CASK p.Val112=

c.336G>A · VCV3680198

Benign Single submitter

Classification

Benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 0.00351%, afr)

Conditions

Intellectual disability, CASK-related, X-linked

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 -0.24	GERP -3.8, phastCons 0.44
Overall
CADD	6.908	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00351% African / African-American · 2/56,922 alleles

Filtering AF 0.000583% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.000218%

Overall 0.000167% 2/1,197,370 alleles · very rare exomes 0/1,085,435 · genomes 2/111,935 · joint denominator

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: CASK
Protein: p.Val112=
Coding: c.336G>A
MANE Select: NM_001367721
Type: single nucleotide variant
Location: chrX:41745544 (GRCh38)
Structure: AlphaFold pLDDT 79.45 · 22 PDB
Residue 112: the protein kinase domain; a UniProt-annotated variant site (found in a patient with epilepsy and pontocerebellar hypoplasia; likely pathogenic)

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

Disease context

Intellectual disability, CASK-related, X-linked — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

CASK p.Val112Met Uncertain significance ★ ⚠ same residue
GPR34 p.Met112Thr Uncertain significance ★ ⚠ same residue
CASK p.Arg489Gln Pathogenic/Likely pathogenic ★★ same condition
CASK p.Ala359Val Uncertain significance ★★ ⚠ same condition
CASK p.Ala833Thr Uncertain significance ★★ ⚠ same condition
CASK p.Arg130Cys Uncertain significance ★★ ⚠ same condition
CASK p.Arg572His Uncertain significance ★★ ⚠ same condition
CASK p.Arg61Trp 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/cask-p-val112 (accessed [today's date]).

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