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Variant (rsID / SNP)

rs886049715

CDK4

rs886049715 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDK4. Location: chromosome 12, position 58,145,077. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CDK4Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
12:58145077
Cytoband
12q14.1
HGVS
NM_000075.4(CDK4):c.267A>G (p.Val89=)
Allele change
Synonymous_V89V

Associated conditions / phenotypes

Melanoma, cutaneous malignant, susceptibility to, 3|Familial melanoma

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.