Q36P (p.Gln36Pro) variant of SRC (P12931)
Q36P (p.Gln36Pro) in SRC (P12931) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
Q36P (p.Gln36Pro) variant details
- p.Gln36Pro
- gnomAD 20-37384260-A-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.369
- REVEL 0.24
- MetaLR 0.22
- MetaSVM -0.78
- CADD 22.40
- PolyPhen-2 0.10
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)
- Structural context available
- SRC SH3 domain domainome 1.0: score -0.112
- Literature evidence available