T39M (p.Thr39Met) variant of F10 (Coagulation factor X)
T39M (p.Thr39Met) in F10 (Coagulation factor X) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
T39M (p.Thr39Met) variant details
- p.Thr39Met
- ExAC rs775307863
- TOPMed rs775307863
- gnomAD rs775307863
- Missense
- Variant Prioritization Score for Impact Estimate 0.396
- REVEL 0.50
- CADD 11.00
- PolyPhen-2 0.01
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available