Is CDKN2A p.Phe5Tyr (c.14T>A) pathogenic?

CDKN2A p.Phe5Tyr (c.14T>A) is classified Uncertain significance in CDKN2A (ClinVar, Multiple submitters, 2 submitters; last evaluated 2023-03-02). Absent from gnomAD v4.1; Associated with hereditary neoplastic syndrome.

What condition is associated with CDKN2A p.Phe5Tyr (c.14T>A)?

CDKN2A p.Phe5Tyr (c.14T>A) is associated with hereditary neoplastic syndrome, familial melanoma (ClinVar).

How common is CDKN2A p.Phe5Tyr (c.14T>A) in the general population?

CDKN2A p.Phe5Tyr (c.14T>A) is absent from gnomAD v4.1 (gnomAD).

CDKN2A p.Phe5Tyr

c.14T>A · rs2131149044 · VCV1436758

Uncertain significance Multiple submitters

Classification

Uncertain significance

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

gnomAD v4.1

Absent

absent from gnomAD v4.1

Conditions

hereditary neoplastic syndrome

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
REVEL	0.276	benign-leaning
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 5	GERP 0.34, phastCons 1
Overall
CADD	20.5	PHRED · no single calibrated threshold — expert panels disagree

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.Phe5Tyr
Coding: c.14T>A
MANE Select: NM_000077 · reported on NM_058195
dbSNP: rs2131149044
Type: single nucleotide variant
Location: chr9:21994318 (GRCh38)
Gene constraint: LOEUF 0.791 · pLI 0.62 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 77.02 · 5 PDB
Residue 5: a β-strand; the 'interaction with cdk5rap3 and mdm2' region

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

Disease context

hereditary neoplastic syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: familial melanoma

Similar variants

CDKN2A p.Ala5Glu Uncertain significance ★★ ⚠ same residue
CDKN2A p.Ala5Thr Uncertain significance ★★ same residue
CDKN2A p.Ala5Val Uncertain significance ★★ ⚠ same residue
CDKN2A p.Phe5Ile Uncertain significance ★★ same residue
CDKN2A p.Phe5Leu Uncertain significance ★★ same residue
CDKN2A p.Ala5= Benign/Likely benign ★★ same residue
CDKN2A p.Phe5= Benign/Likely benign ★★ same residue
CDKN2A p.Phe5Ser 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-phe5tyr (accessed [today's date]).

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