P9T (p.Pro9Thr) variant of MET (P08581)
P9T (p.Pro9Thr) in MET (P08581) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Renal cell carcinoma. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes structural context.
P9T (p.Pro9Thr) variant details
- p.Pro9Thr
- rs2116578170
- ClinGen CA368968185
- cosmic curated COSV59256
- ClinVar RCV002019146
- Uncertain significance
- Renal cell carcinoma
- Missense
- Variant Prioritization Score for Impact Estimate 0.344
- AlphaMissense 0.12
- MetaLR 0.29
- MetaSVM -0.67
- PolyPhen-2 0.10
- SIFT 0.16
- EVE 0.09
- ClinVar: Uncertain significance (Renal cell carcinoma)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available