P18R (p.Pro18Arg) variant of CCND1 (G1/S-specific cyclin-D1)
P18R (p.Pro18Arg) in CCND1 (G1/S-specific cyclin-D1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
P18R (p.Pro18Arg) variant details
- p.Pro18Arg
- NCI-TCGA Cosmic COSV5712
- cosmic curated COSV57122
- Ensembl rs2120080068
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.246
- REVEL 0.10
- CADD 18.90
- PolyPhen-2 0.00
- SIFT 0.80
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available