P94S (p.Pro94Ser) variant of F13B (Coagulation factor XIII B chain)
P94S (p.Pro94Ser) in F13B (Coagulation factor XIII B chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.73 / 1. The record also includes population frequency data and structural context.
P94S (p.Pro94Ser) variant details
- p.Pro94Ser
- TOPMed rs906803283
- gnomAD rs906803283
- Missense
- Variant Prioritization Score for Impact Estimate 0.731
- REVEL 0.70
- CADD 26.10
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available