S97T (p.Ser97Thr) variant of LRP2 (P98164)
S97T (p.Ser97Thr) in LRP2 (P98164) 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 0.72 / 1. The record also includes structural context.
S97T (p.Ser97Thr) variant details
- p.Ser97Thr
- rs1468975390
- NCI-TCGA Cosmic COSV5556
- cosmic curated COSV55560
- TOPMed rs1468975390
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.72
- AlphaMissense 0.13
- MetaLR 0.92
- MetaSVM 0.94
- PolyPhen-2 0.92
- SIFT 0.08
- MutPred 0.63
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available