p.Leu18 Leu19del variant of RET (P07949)
p.Leu18 Leu19del in RET (P07949) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data, published literature, and structural context.
p.Leu18 Leu19del variant details
- rs768132465
- gnomAD 10-43077301-TTGCT
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.465
- CADD 18.70
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available
- Literature evidence available