L18V (p.Leu18Val) variant of F13B (Coagulation factor XIII B chain)
L18V (p.Leu18Val) in F13B (Coagulation factor XIII B chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
L18V (p.Leu18Val) variant details
- p.Leu18Val
- gnomAD rs1183401714
- Missense
- Variant Prioritization Score for Impact Estimate 0.196
- REVEL 0.05
- CADD 19.20
- PolyPhen-2 0.07
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available