G117A (p.Gly117Ala) variant of F13B (Coagulation factor XIII B chain)
G117A (p.Gly117Ala) in F13B (Coagulation factor XIII B chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data and structural context.
G117A (p.Gly117Ala) variant details
- p.Gly117Ala
- gnomAD rs1655875490
- Missense
- Variant Prioritization Score for Impact Estimate 0.139
- REVEL 0.05
- CADD 9.10
- PolyPhen-2 0.17
- SIFT 0.30
- Most common in the Latino/Admixed American population (allele frequency 6.6e-05)
- Structural context available