N21D (p.Asn21Asp) variant of CCND1 (G1/S-specific cyclin-D1)
N21D (p.Asn21Asp) 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 0.34 / 1. The record also includes population frequency data and structural context.
N21D (p.Asn21Asp) variant details
- p.Asn21Asp
- rs766170770
- NCI-TCGA Cosmic COSV9991
- cosmic curated COSV99919
- ExAC rs766170770
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.341
- REVEL 0.15
- CADD 23.20
- PolyPhen-2 0.27
- SIFT 0.37
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available