A11T (p.Ala11Thr) variant of SRC (P12931)
A11T (p.Ala11Thr) in SRC (P12931) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data, experimental measurements, and structural context.
A11T (p.Ala11Thr) variant details
- p.Ala11Thr
- TOPMed rs1318197870
- gnomAD rs1318197870
- Missense
- Variant Prioritization Score for Impact Estimate 0.27
- REVEL 0.09
- CADD 22.50
- PolyPhen-2 0.01
- SIFT 0.45
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- SRC SH3 domain domainome 1.0: score -1.08