P38T (p.Pro38Thr) variant of SRC (P12931)
P38T (p.Pro38Thr) in SRC (P12931) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data, experimental measurements, and structural context.
P38T (p.Pro38Thr) variant details
- p.Pro38Thr
- TOPMed rs2070410985
- Missense
- Variant Prioritization Score for Impact Estimate 0.43
- REVEL 0.25
- CADD 25.40
- PolyPhen-2 1.00
- SIFT 0.04
- Population evidence available
- Structural context available
- SRC SH3 domain domainome 1.0: score -0.945