Is CDKN2A p.Gly6Trp (c.15_16delinsCT) pathogenic?

CDKN2A p.Gly6Trp (c.1516delinsCT) is classified Uncertain significance in CDKN2A (ClinVar, Single submitter, 1 submitter; last evaluated 2025-04-29). Absent from gnomAD; Associated with familial melanoma.

What condition is associated with CDKN2A p.Gly6Trp (c.15_16delinsCT)?

CDKN2A p.Gly6Trp (c.15_16delinsCT) is associated with familial melanoma (ClinVar).

How common is CDKN2A p.Gly6Trp (c.15_16delinsCT) in the general population?

CDKN2A p.Gly6Trp (c.15_16delinsCT) is absent from gnomAD (gnomAD).

How is Familial melanoma inherited?

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

CDKN2A p.Gly6Trp

c.15_16delinsCT · rs2131114105 · VCV1508121

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Not reported

no gnomAD frequency available for this variant

Conditions

familial melanoma

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	—	not assessed · substitutions only
Constraint at this position
Conservation	phyloP 0.075	GERP -0.94, phastCons 0.006
Regional constraint	o/e 1.13	unconstrained · MANE · 6,595 bp · p 0.04 · regional, not allelic
Region caveats
Repeat context	tandem	GGCTCCATGCTGCTCCCCGCCGCC simple repeat · ambiguous alignment · confidence, not pathogenicity

Population frequency

dbSNP / gnomAD

No gnomAD frequency available for this variant. 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: CDKN2A
Protein: p.Gly6Trp
Coding: c.15_16delinsCT
MANE Select: NM_000077
dbSNP: rs2131114105
Type: Indel
Location: chr9:21974812 (GRCh38)
Gene constraint: LOEUF 0.791 · pLI 0.62 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 77.02 · 5 PDB
Residue 6: 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

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.Gly6Ala Uncertain significance ★★ ⚠ same residue
CDKN2A p.Gly6Arg Uncertain significance ★★ ⚠ same residue
CDKN2A p.Gly6Val Uncertain significance ★★ ⚠ same residue
CDKN2A p.Gly6Glu Conflicting classifications of pathogenicity ★ ⚠ same residue
CDKN2A p.Gly6= Likely benign ★ same residue
CDKN2A p.Ala68Leu Likely pathogenic ★★ same condition
CDKN2A p.Arg128fs Likely pathogenic ★★ same condition
CDKN2A p.Ala85Phe 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/cdkn2a-p-gly6trp (accessed [today's date]).

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