Is CDKN1C p.Ala37= (c.111C>T) pathogenic?

CDKN1C p.Ala37= (c.111C>T) is classified Likely benign in CDKN1C (ClinVar, Multiple submitters, 2 submitters; last evaluated 2024-02-04). Ultra-rare (popmax 0.0137%, eas); Associated with Beckwith-Wiedemann syndrome.

What condition is associated with CDKN1C p.Ala37= (c.111C>T)?

CDKN1C p.Ala37= (c.111C>T) is associated with Beckwith-Wiedemann syndrome (ClinVar).

How common is CDKN1C p.Ala37= (c.111C>T) in the general population?

CDKN1C p.Ala37= (c.111C>T) is ultra-rare (popmax 0.0137%, eas) (gnomAD).

CDKN1C p.Ala37=

c.111C>T · rs769255937 · VCV1146771

Likely benign Multiple submitters

Classification

Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

gnomAD v4.1

Rare

ultra-rare (popmax 0.0137%, eas)

Conditions

Beckwith-Wiedemann syndrome

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 0.84	GERP -2.3, phastCons 0.38
Overall
CADD	9.591	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0137% East Asian · 6/43,852 alleles

Filtering AF 0.0059% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00401%

Overall 0.000502% 8/1,595,122 alleles · ultra-rare

Ancestry group	Frequency	1 in
East Asiangrpmax	0.0137%	7,309
European (non-Finnish)	0.00017%	586,558

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: CDKN1C
Protein: p.Ala37=
Coding: c.111C>T
MANE Select: NM_001122630
dbSNP: rs769255937
Type: single nucleotide variant
Location: chr11:2885346 (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.Ala37Val Uncertain significance ★★ ⚠ same residue
CDKN1C p.Ala37Asp Uncertain significance ★ ⚠ 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
CDKN1C p.Gln230Ter Pathogenic ★★ same condition
CDKN1C p.Glu119Ter 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-ala37 (accessed [today's date]).

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