D138N (p.Asp138Asn) variant of F13B (Coagulation factor XIII B chain)
D138N (p.Asp138Asn) in F13B (Coagulation factor XIII B chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
D138N (p.Asp138Asn) variant details
- p.Asp138Asn
- ExAC rs765498516
- TOPMed rs765498516
- gnomAD rs765498516
- Missense
- Variant Prioritization Score for Impact Estimate 0.117
- REVEL 0.08
- CADD 15.20
- PolyPhen-2 0.01
- SIFT 0.15
- Most common in the Latino/Admixed American population (allele frequency 6.6e-05)
- Structural context available