C118S (p.Cys118Ser) variant of F13B (Coagulation factor XIII B chain)
C118S (p.Cys118Ser) in F13B (Coagulation factor XIII B chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.78 / 1. The record also includes population frequency data and structural context.
C118S (p.Cys118Ser) variant details
- p.Cys118Ser
- Ensembl rs1048993590
- Missense
- Variant Prioritization Score for Impact Estimate 0.782
- REVEL 0.90
- CADD 24.00
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-06)
- Structural context available