Q36H (p.Gln36His) variant of SRC (P12931)
Q36H (p.Gln36His) in SRC (P12931) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data, experimental measurements, and structural context.
Q36H (p.Gln36His) variant details
- p.Gln36His
- gnomAD rs55962640
- Missense
- Variant Prioritization Score for Impact Estimate 0.349
- REVEL 0.14
- CADD 22.20
- PolyPhen-2 0.36
- SIFT 0.31
- Population evidence available
- Structural context available
- SRC SH3 domain domainome 1.0: score -0.112