Annotation Detail
Information
- Associated Genes
- CDK4 LOC130008148
- Associated Variants
-
CDK4 p.Asn41Ser (p.N41S)
(
ENST00000312990.10,
ENST00000549606.5,
ENST00000257904.11 )
CDK4 p.Asn41Ser (p.N41S) ( ENST00000257904.11, ENST00000312990.10, ENST00000549606.5 ) - Associated Disease
- Melanoma, cutaneous malignant, susceptibility to, 3
- Source Database
- ClinVar
- Description
- NM_000075.4(CDK4):c.122A>G (p.Asn41Ser) AND Melanoma, cutaneous malignant, susceptibility to, 3
- ClinVar Allele ID
- 139534
- ClinVar RefSeq Alternation Syntax
- NM_000075.4:c.122A>G
- Clinical Significance Description
- Conflicting interpretations of pathogenicity
- Clinical Significance Last Update
- 2023-11-07
- Clinical Significance Review Status
- criteria provided, conflicting interpretations
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000662895
- ClinVar Disease
- Melanoma, cutaneous malignant, susceptibility to, 3
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs