M49I (p.Met49Ile) variant of F13B (Coagulation factor XIII B chain)
M49I (p.Met49Ile) in F13B (Coagulation factor XIII B chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
M49I (p.Met49Ile) variant details
- p.Met49Ile
- ExAC rs776286731
- TOPMed rs776286731
- gnomAD rs776286731
- Missense
- Variant Prioritization Score for Impact Estimate 0.466
- REVEL 0.31
- CADD 24.70
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the Latino/Admixed American population (allele frequency 6.7e-05)
- Structural context available