Y37N (p.Tyr37Asn) variant of SRSF2 (Q01130)
Y37N (p.Tyr37Asn) in SRSF2 (Q01130) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.83 / 1. The record also includes population frequency data and published literature.
Y37N (p.Tyr37Asn) variant details
- p.Tyr37Asn
- gnomAD 17-76737052-A-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.828
- REVEL 0.93
- CADD 32.00
- SIFT 0.01
- Population evidence available
- Literature evidence available