Is CIC p.Val2098Met (c.6292G>A) pathogenic?

CIC p.Val2098Met (c.6292G>A) is classified Uncertain significance in CIC (ClinVar, Multiple submitters, 2 submitters; last evaluated 2022-10-01). AlphaMissense: ambiguous (0.4938); Ultra-rare (popmax 0.0324%, nfe); Associated with intellectual developmental disorder, autosomal dominant 45.

What condition is associated with CIC p.Val2098Met (c.6292G>A)?

CIC p.Val2098Met (c.6292G>A) is associated with intellectual developmental disorder, autosomal dominant 45 (ClinVar).

How common is CIC p.Val2098Met (c.6292G>A) in the general population?

CIC p.Val2098Met (c.6292G>A) is ultra-rare (popmax 0.0324%, nfe) (gnomAD).

What do computational predictors say about CIC p.Val2098Met (c.6292G>A)?

AlphaMissense predicts ambiguous (score 0.4938) — an in-silico prediction, not a clinical call.

CIC p.Val2098Met

c.6292G>A · rs202242046 · VCV1325506

Uncertain significance Multiple submitters

Classification

Uncertain significance

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

AlphaMissense

ambiguous

0.4938 · ACMG-weighted

gnomAD v4.1

Rare

ultra-rare (popmax 0.0324%, nfe)

Conditions

intellectual developmental disorder, autosomal dominant 45

Computational evidence

Protein change
AlphaMissense	0.4938	ambiguous
REVEL	0.207	benign-leaning
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 12	GERP 1.5, phastCons 1
Overall
CADD	26.7	PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

⚠ Isoform check: AlphaMissense numbered on a different transcript (AM V1189M vs ClinVar V2098M) — verify the residue.

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0324% European (non-Finnish) · 382/1,179,778 alleles

Filtering AF 0.0297% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0286%

Overall 0.0244% 393/1,612,624 alleles · ultra-rare

Ancestry group	Frequency	1 in
European (non-Finnish)grpmax	0.0324%	3,088
Remaining individualsnot grpmax-eligible	0.00961%	10,404
African / African-American	0.004%	24,975
East Asian	0.00223%	44,876
Finnishnot grpmax-eligible	0.00159%	63,064

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: CIC
Protein: p.Val2098Met
Coding: c.6292G>A
MANE Select: NM_005984 · reported on NM_001386298
dbSNP: rs202242046
Type: single nucleotide variant
Location: chr19:42293051 (GRCh38)
Structure: AlphaFold pLDDT 75.09

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

Disease context

intellectual developmental disorder, autosomal dominant 45 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

CIC c.3179+1G>T Pathogenic ★★ same condition
CIC c.5903-2A>G Likely pathogenic ★★ same condition
CIC p.Asn1136Ser Likely pathogenic ★★ same condition
CIC p.Gln1134Ter Pathogenic ★★ same condition
CIC p.Gln1799Ter Likely pathogenic ★★ same condition
CIC p.Ala1761Val Uncertain significance ★★ ⚠ same condition
CIC p.Ala2064Thr Uncertain significance ★★ ⚠ same condition
CIC p.Ala2463Thr 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/cic-p-val2098met (accessed [today's date]).

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