p.Leu14 Leu15insTrp variant of RET (P07949)
p.Leu14 Leu15insTrp in RET (P07949) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data, published literature, and structural context.
p.Leu14 Leu15insTrp variant details
- rs2132498515
- gnomAD 10-43077301-T-TGG
- Inframe Insertion
- Variant Prioritization Score for Impact Estimate 0.451
- CADD 16.80
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available