P17P (p.Pro17Pro) variant of MCCC2 (Q9HCC0)
P17P (p.Pro17Pro) in MCCC2 (Q9HCC0) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data, published literature, and structural context.
P17P (p.Pro17Pro) variant details
- p.Pro17Pro
- rs1390205513
- gnomAD 5-71587476-C-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.259
- CADD 6.72
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available