R138G (p.Arg138Gly) variant of F13A1 (Coagulation factor XIII A chain)
R138G (p.Arg138Gly) in F13A1 (Coagulation factor XIII A chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
R138G (p.Arg138Gly) variant details
- p.Arg138Gly
- gnomAD rs1424720526
- Missense
- Variant Prioritization Score for Impact Estimate 0.317
- REVEL 0.31
- MetaLR 0.34
- MetaSVM -0.71
- CADD 23.00
- PolyPhen-2 0.06
- SIFT 0.14
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Structural context available