P21L (p.Pro21Leu) variant of CD3D (P04234)
P21L (p.Pro21Leu) in CD3D (P04234) 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 0.06 / 1. The record also includes population frequency data and structural context.
P21L (p.Pro21Leu) variant details
- p.Pro21Leu
- NCI-TCGA Cosmic COSV5267
- cosmic curated COSV52676
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.0596
- REVEL 0.04
- CADD 2.77
- PolyPhen-2 0.02
- SIFT 0.41
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the HGDP:YAKUT population (allele frequency 0.04)
- Structural context available