P20P (p.Pro20Pro) variant of RET (P07949)
P20P (p.Pro20Pro) in RET (P07949) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data, published literature, and structural context.
P20P (p.Pro20Pro) variant details
- p.Pro20Pro
- rs1263991822
- gnomAD 10-43077318-G-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.433
- CADD 14.90
- Most common in the Non-Finnish European population (allele frequency 2.3e-05)
- Structural context available
- Literature evidence available