Q13H (p.Gln13His) variant of SRC (P12931)
Q13H (p.Gln13His) in SRC (P12931) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
Q13H (p.Gln13His) variant details
- p.Gln13His
- gnomAD 20-37384192-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.269
- REVEL 0.21
- MetaLR 0.24
- MetaSVM -0.77
- CADD 22.50
- PolyPhen-2 0.00
- SIFT 0.05
- Population evidence available
- Structural context available
- SRC SH3 domain domainome 1.0: score -0.0545
- Literature evidence available