P16S (p.Pro16Ser) variant of F13A1 (Coagulation factor XIII A chain)
P16S (p.Pro16Ser) in F13A1 (Coagulation factor XIII A chain) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.48 / 1. The record also includes population frequency data and structural context.
P16S (p.Pro16Ser) variant details
- p.Pro16Ser
- NCI-TCGA Cosmic COSV5355
- NCI-TCGA Cosmic COSV5356
- Ensembl rs2113207212
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.481
- REVEL 0.31
- MetaLR 0.53
- MetaSVM 0.11
- CADD 24.10
- PolyPhen-2 0.77
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available