P11P (p.Pro11Pro) variant of MCCC2 (Q9HCC0)
P11P (p.Pro11Pro) in MCCC2 (Q9HCC0) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data, published literature, and structural context.
P11P (p.Pro11Pro) variant details
- p.Pro11Pro
- rs770765635
- gnomAD 5-71587458-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.131
- CADD 7.13
- Most common in the Finnish in Finland (FIN) population (allele frequency 2.8e-05)
- Structural context available
- Literature evidence available