T37M (p.Thr37Met) variant of F11 (Coagulation factor XI)
T37M (p.Thr37Met) in F11 (Coagulation factor XI) 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 0.55 / 1. The record also includes population frequency data and structural context.
T37M (p.Thr37Met) variant details
- p.Thr37Met
- rs1377806811
- cosmic curated COSV10510
- TOPMed rs1377806811
- gnomAD rs1377806811
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.554
- AlphaMissense 0.09
- MetaLR 0.80
- MetaSVM 0.28
- PolyPhen-2 1.00
- SIFT 0.00
- EVE 0.20
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available