G28G (p.Gly28Gly) variant of SRC (P12931)
G28G (p.Gly28Gly) in SRC (P12931) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
G28G (p.Gly28Gly) variant details
- p.Gly28Gly
- rs2147049683
- gnomAD 20-37384237-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.112
- CADD 4.40
- Most common in the Finnish in Finland (FIN) population (allele frequency 2.4e-05)
- Structural context available
- SRC SH3 domain domainome 1.0: score -0.128
- Literature evidence available