H29Q (p.His29Gln) variant of F13B (Coagulation factor XIII B chain)
H29Q (p.His29Gln) in F13B (Coagulation factor XIII B chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
H29Q (p.His29Gln) variant details
- p.His29Gln
- Ensembl rs900935516
- Missense
- Variant Prioritization Score for Impact Estimate 0.0895
- REVEL 0.06
- CADD 9.65
- PolyPhen-2 0.02
- SIFT 0.41
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available