P78L (p.Pro78Leu) variant of CD79A (P11912)
P78L (p.Pro78Leu) in CD79A (P11912) 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 0.16 / 1. The record also includes population frequency data and structural context.
P78L (p.Pro78Leu) variant details
- p.Pro78Leu
- NCI-TCGA Cosmic COSV5573
- cosmic curated COSV55738
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.164
- REVEL 0.10
- CADD 16.80
- PolyPhen-2 0.27
- SIFT 0.04
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available