P16S (p.Pro16Ser) variant of GNA13 (Q14344)
P16S (p.Pro16Ser) in GNA13 (Q14344) 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 0.62 / 1. The record also includes population frequency data.
P16S (p.Pro16Ser) variant details
- p.Pro16Ser
- rs781422742
- ExAC rs781422742
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.624
- REVEL 0.62
- MetaLR 0.64
- MetaSVM 0.37
- CADD 24.20
- PolyPhen-2 1.00
- SIFT 0.20
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)