N4H (p.Asn4His) variant of SRC (P12931)
N4H (p.Asn4His) in SRC (P12931) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data, experimental measurements, and structural context.
N4H (p.Asn4His) variant details
- p.Asn4His
- gnomAD rs1320051629
- Missense
- Variant Prioritization Score for Impact Estimate 0.343
- REVEL 0.16
- CADD 22.20
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- SRC SH3 domain domainome 1.0: score -0.384