G26G (p.Gly26Gly) variant of SRC (P12931)
G26G (p.Gly26Gly) in SRC (P12931) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
G26G (p.Gly26Gly) variant details
- p.Gly26Gly
- rs2147049619
- gnomAD 20-37384231-C-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0877
- CADD 1.00
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)
- Structural context available
- SRC SH3 domain domainome 1.0: score -0.0804
- Literature evidence available