R14W (p.Arg14Trp) variant of CCND3 (G1/S-specific cyclin-D3)
R14W (p.Arg14Trp) in CCND3 (G1/S-specific cyclin-D3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data and structural context.
R14W (p.Arg14Trp) variant details
- p.Arg14Trp
- cosmic curated COSV65912
- ExAC rs762507772
- TOPMed rs762507772
- gnomAD rs762507772
- Missense
- Variant Prioritization Score for Impact Estimate 0.445
- REVEL 0.18
- CADD 32.00
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 7.4e-05)
- Structural context available