p.Pro20dup variant of RET (P07949)
p.Pro20dup in RET (P07949) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes population frequency data, published literature, and structural context.
p.Pro20dup variant details
- rs1064796534
- gnomAD 10-43077314-T-TGC
- Inframe Insertion
- Variant Prioritization Score for Impact Estimate 0.489
- CADD 22.40
- Most common in the 1KG:IBS population (allele frequency 0.017)
- Structural context available
- Literature evidence available