N23N (p.Asn23Asn) variant of SRC (P12931)
N23N (p.Asn23Asn) in SRC (P12931) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
N23N (p.Asn23Asn) variant details
- p.Asn23Asn
- rs754332476
- gnomAD 20-37384222-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.277
- CADD 7.45
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- SRC SH3 domain domainome 1.0: score -0.878
- Literature evidence available