Y38C (p.Tyr38Cys) variant of F13B (Coagulation factor XIII B chain)
Y38C (p.Tyr38Cys) in F13B (Coagulation factor XIII B chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
Y38C (p.Tyr38Cys) variant details
- p.Tyr38Cys
- gnomAD rs1199651158
- Missense
- Variant Prioritization Score for Impact Estimate 0.388
- REVEL 0.39
- CADD 24.60
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available