P42L (p.Pro42Leu) variant of TNFRSF13B (O14836)
P42L (p.Pro42Leu) in TNFRSF13B (O14836) 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 0.30 / 1. The record also includes population frequency data.
P42L (p.Pro42Leu) variant details
- p.Pro42Leu
- rs770198071
- NCI-TCGA Cosmic COSV9989
- cosmic curated COSV99891
- ExAC rs770198071
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.302
- REVEL 0.26
- CADD 9.14
- PolyPhen-2 0.38
- SIFT 0.22
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the REMAINING population (allele frequency 1.7e-05)