V10A (p.Val10Ala) variant of SRSF2 (Q01130)
V10A (p.Val10Ala) in SRSF2 (Q01130) 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 0.57 / 1. The record also includes population frequency data.
V10A (p.Val10Ala) variant details
- p.Val10Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.565
- REVEL 0.50
- CADD 29.20
- PolyPhen-2 0.84
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)