V132M (p.Val132Met) variant of F13B (Coagulation factor XIII B chain)
V132M (p.Val132Met) in F13B (Coagulation factor XIII B chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
V132M (p.Val132Met) variant details
- p.Val132Met
- gnomAD rs1399927293
- Missense
- Variant Prioritization Score for Impact Estimate 0.205
- REVEL 0.07
- CADD 15.90
- Most common in the Latino/Admixed American population (allele frequency 6.6e-05)
- Structural context available