L18L (p.Leu18Leu) variant of RET (P07949)
L18L (p.Leu18Leu) in RET (P07949) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data, published literature, and structural context.
L18L (p.Leu18Leu) variant details
- p.Leu18Leu
- rs2132498926
- gnomAD 10-43077310-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.314
- CADD 14.70
- Most common in the Finnish in Finland (FIN) population (allele frequency 3.8e-05)
- Structural context available
- Literature evidence available