Q13R (p.Gln13Arg) variant of SRC (P12931)
Q13R (p.Gln13Arg) in SRC (P12931) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data, experimental measurements, and structural context.
Q13R (p.Gln13Arg) variant details
- p.Gln13Arg
- TOPMed rs1250842919
- gnomAD rs1250842919
- Missense
- Variant Prioritization Score for Impact Estimate 0.256
- REVEL 0.15
- CADD 22.50
- PolyPhen-2 0.02
- SIFT 0.10
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- SRC SH3 domain domainome 1.0: score -0.0545