S2R (p.Ser2Arg) variant of SRSF2 (Q01130)
S2R (p.Ser2Arg) 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 0.22 / 1. The record also includes population frequency data.
S2R (p.Ser2Arg) variant details
- p.Ser2Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.22
- REVEL 0.17
- CADD 23.00
- PolyPhen-2 0.94
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available