R15P (p.Arg15Pro) variant of SRC (P12931)
R15P (p.Arg15Pro) 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, published literature, and structural context.
R15P (p.Arg15Pro) variant details
- p.Arg15Pro
- gnomAD 20-37384197-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.43
- REVEL 0.26
- MetaLR 0.25
- MetaSVM -0.57
- CADD 23.30
- PolyPhen-2 0.04
- SIFT 0.17
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- SRC SH3 domain domainome 1.0: score -0.372
- Literature evidence available