Is CDKN2A p.Glu10Ter (c.28G>T) pathogenic?

CDKN2A p.Glu10Ter (c.28G>T) is classified Pathogenic in CDKN2A (ClinVar, Single submitter, 1 submitter; last evaluated 2022-05-30). Absent from gnomAD v4.1; Associated with familial melanoma.

What condition is associated with CDKN2A p.Glu10Ter (c.28G>T)?

CDKN2A p.Glu10Ter (c.28G>T) is associated with familial melanoma (ClinVar).

How common is CDKN2A p.Glu10Ter (c.28G>T) in the general population?

CDKN2A p.Glu10Ter (c.28G>T) is absent from gnomAD v4.1 (gnomAD).

How is Familial melanoma inherited?

Typically Autosomal dominant, Multigenic/multifactorial (Orphanet). A genetic counselor can assess individual risk for a family.

CDKN2A p.Glu10Ter

c.28G>T · rs2131113914 · VCV2000887

Pathogenic Single submitter

Classification

Pathogenic

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

Consequence

nonsense (stop-gain)

predicted LoF

gnomAD v4.1

Absent

absent from gnomAD v4.1

Conditions

familial melanoma

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Consequence	nonsense (stop-gain)	predicted loss-of-function in a haploinsufficient gene (ClinGen)
NMD	predicted	premature termination codon in exon 1 of 3
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 0.075	GERP 2, phastCons 0.22
Overall
CADD	35.0	PHRED · no single calibrated threshold — expert panels disagree

Predicted loss-of-function is descriptive, not an applied PVS1 code.

Population frequency

gnomAD v4.1 · exomes + genomes

Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.

Variant & gene context

Gene: CDKN2A
Protein: p.Glu10Ter
Coding: c.28G>T
MANE Select: NM_000077
dbSNP: rs2131113914
Type: single nucleotide variant
Location: chr9:21974800 (GRCh38)
Gene constraint: LOEUF 0.791 · pLI 0.62 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 77.02 · 5 PDB
Residue 10: the 'interaction with cdk5rap3 and mdm2' region

Full CDKN2A gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

familial melanoma — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Familial melanoma (Orphanet):

Inheritance: Autosomal dominant, Multigenic/multifactorial
Onset: Adult
Prevalence: 1-9 / 100 000 (Europe)

Similar variants

CDKN2A p.Arg10Gly Uncertain significance ★★ same residue
CDKN2A p.Glu10Lys Uncertain significance ★★ ⚠ same residue
CDKN2A p.Arg10= Benign/Likely benign ★★ same residue
CDKN2A p.Glu10= Likely benign ★ same residue
CDKN2A p.Glu10fs Pathogenic ★ same residue
CDKN2A p.Arg10Gln Uncertain significance ★ same residue
CDKN2A p.Arg10Trp Uncertain significance ★ same residue
CDKN2A p.Glu10Ala Uncertain significance ★ ⚠ same residue

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/cdkn2a-p-glu10ter (accessed [today's date]).

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