T78A (p.Thr78Ala) variant of F13B (Coagulation factor XIII B chain)
T78A (p.Thr78Ala) in F13B (Coagulation factor XIII B chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data and structural context.
T78A (p.Thr78Ala) variant details
- p.Thr78Ala
- TOPMed rs1249711828
- gnomAD rs1249711828
- Missense
- Variant Prioritization Score for Impact Estimate 0.0649
- REVEL 0.06
- CADD 0.00
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available