Is CDKN1C p.Val98Phe (c.292G>T) pathogenic?

CDKN1C p.Val98Phe (c.292G>T) is classified Uncertain significance in CDKN1C (ClinVar, Single submitter, 1 submitter; last evaluated 2022-09-06). AlphaMissense: likely benign (0.2674); No allele count reported in gnomAD v4.1 (AN 1,525,796); Associated with Beckwith-Wiedemann syndrome.

What condition is associated with CDKN1C p.Val98Phe (c.292G>T)?

CDKN1C p.Val98Phe (c.292G>T) is associated with Beckwith-Wiedemann syndrome (ClinVar).

How common is CDKN1C p.Val98Phe (c.292G>T) in the general population?

CDKN1C p.Val98Phe (c.292G>T) is no allele count reported in gnomAD v4.1 (AN 1,525,796) (gnomAD).

What do computational predictors say about CDKN1C p.Val98Phe (c.292G>T)?

AlphaMissense predicts likely benign (score 0.2674) — an in-silico prediction, not a clinical call.

CDKN1C p.Val98Phe

c.292G>T · rs2133785299 · VCV1522308

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.2674 · ACMG-weighted

gnomAD v4.1

Not reported

no allele count reported in gnomAD v4.1 (AN 1,525,796)

Missense predictors

1/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

Beckwith-Wiedemann syndrome

Computational evidence

Protein change
AlphaMissense	0.2674	likely benign
REVEL	0.123	moderately benign-leaning
SaProt	LLR -11.18	damaging
⇒ SaProt calls this damaging; AlphaMissense and REVEL do not.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 2.2	GERP -1.6, phastCons 1
Overall
CADD	18.78	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 V109F vs ClinVar V98F) — verify the residue.

Population frequency

gnomAD v4.1 · exomes + genomes

No allele count reported in gnomAD v4.1 (AN 1,525,796). This is missing data, not an absence: the variant may or may not be present in gnomAD. Rarity (ACMG PM2) and BA1/BS1 cannot be assessed for it.

Variant & gene context

Gene: CDKN1C
Protein: p.Val98Phe
Coding: c.292G>T
MANE Select: NM_001122630
dbSNP: rs2133785299
Type: single nucleotide variant
Location: chr11:2885165 (GRCh38)
Gene constraint: LOEUF 1.943 · pLI <0.01 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 63.93

Full CDKN1C gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Beckwith-Wiedemann syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

CDKN1C p.Val98Ala Uncertain significance ★ ⚠ same residue
CDKN1C p.Val98Ile Uncertain significance ★ ⚠ same residue
CDKN1C p.Val98Leu Uncertain significance ★ ⚠ same residue
CDKN1C p.Val98= Likely benign ★ same residue
CDKN1C p.Asp263Asn Pathogenic ★★ ⚠ same condition
CDKN1C p.Cys19Ter Pathogenic/Likely pathogenic ★★ same condition
CDKN1C p.Gln219Ter Pathogenic ★★ same condition
CDKN1C p.Gln221Ter 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/cdkn1c-p-val98phe (accessed [today's date]).

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