Melanoma-pancreatic cancer syndrome: genes and variants

Melanoma-pancreatic cancer syndrome is linked to 1 analyzed protein (CDKN2A). 11 DNA variants are known to cause it; 22 more are uncertain, and 0 of those already look disease-causing on computable evidence.

Last updated 2026-09-30. Research information, not medical advice.

Genes linked to Melanoma-pancreatic cancer syndrome

Known disease-causing variants in Melanoma-pancreatic cancer syndrome

VariantPositionProtein partClinical label
CDKN2A S73R73Disease-causing (★★)
CDKN2A R82L82Disease-causing (★★)
CDKN2A R98Q98Disease-causing (★★)
CDKN2A V46G46Interaction with CDK5RAP3 and MDM2Disease-causing (★★)
CDKN2A M48I48Interaction with CDK5RAP3 and MDM2Disease-causing (★★)
CDKN2A S52I52Interaction with CDK5RAP3 and MDM2Disease-causing (★★)
CDKN2A Q70H70Disease-causing (★★)
CDKN2A A76L76Disease-causing (★★)
CDKN2A L86M86Disease-causing (★★)
CDKN2A R87W87Disease-causing (★★)
CDKN2A G125R125Disease-causing (★★)

Which prediction tools work for Melanoma-pancreatic cancer syndrome

How often each tool ranks a disease-causing variant above a harmless one (AUROC × 100).

Same protein, different disease

Diseases related to Melanoma-pancreatic cancer syndrome

Frequently asked questions

Which genes are linked to Melanoma-pancreatic cancer syndrome?

In CATVariant, Melanoma-pancreatic cancer syndrome is linked to 1 analyzed protein: CDKN2A (Tumor suppressor ARF).

How many genetic variants are linked to Melanoma-pancreatic cancer syndrome?

34 variants: 11 are classified as disease-causing (pathogenic or likely pathogenic) in ClinVar and 22 are of uncertain significance or have conflicting reports.

Which uncertain variants in Melanoma-pancreatic cancer syndrome look disease-causing?

None of the uncertain variants currently reaches the likely-pathogenic range on computable evidence alone.

Which variant effect predictor works best for Melanoma-pancreatic cancer syndrome?

Among tools not trained on clinical labels, SIFT separates this disease's known disease-causing variants from harmless ones best (AUROC 0.72, based on 8 disease-causing and 33 harmless variants).

About this data

Variant–disease links come from ClinVar, Open Targets and UniProt, pooled from the latest public CATVariant analysis of each human protein. Evidence scores use the ACMG/AMP Bayesian points scale with computable criteria only (position among known disease variants, rarity in gnomAD, calibrated predictors, deep mutational scanning); there is no family or patient data, so they prioritise variants for expert review and never classify them.

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