T77A (p.Thr77Ala) variant of F13B (Coagulation factor XIII B chain)
T77A (p.Thr77Ala) in F13B (Coagulation factor XIII B chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
T77A (p.Thr77Ala) variant details
- p.Thr77Ala
- TOPMed rs546919954
- Missense
- Variant Prioritization Score for Impact Estimate 0.351
- REVEL 0.30
- CADD 23.40
- PolyPhen-2 0.93
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 6.3e-06)
- Structural context available