P38H (p.Pro38His) variant of SRC (P12931)
P38H (p.Pro38His) in SRC (P12931) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
P38H (p.Pro38His) variant details
- p.Pro38His
- gnomAD 20-37384266-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.491
- REVEL 0.31
- MetaLR 0.50
- MetaSVM -0.08
- CADD 27.40
- PolyPhen-2 1.00
- SIFT 0.00
- Population evidence available
- Structural context available
- SRC SH3 domain domainome 1.0: score -0.945
- Literature evidence available