p.Gly28 Ala31del variant of SRC (P12931)
p.Gly28 Ala31del in SRC (P12931) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
p.Gly28 Ala31del variant details
- gnomAD 20-37384228-CGGCG
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.204
- CADD 17.40
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)
- Structural context available
- SRC SH3 domain domainome 1.0: score -0.128
- Literature evidence available