R39M (p.Arg39Met) variant of LCK (Tyrosine-protein kinase Lck)
R39M (p.Arg39Met) in LCK (Tyrosine-protein kinase Lck) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
R39M (p.Arg39Met) variant details
- p.Arg39Met
- rs1234158033
- gnomAD 1-32274226-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.329
- CADD 15.30
- Most common in the Finnish in Finland (FIN) population (allele frequency 2.1e-05)
- Structural context available
- LCK SH3 domain domainome 1.0: score -0.468
- Literature evidence available