P14P (p.Pro14Pro) variant of MCM2 (P49736)
P14P (p.Pro14Pro) in MCM2 (P49736) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
P14P (p.Pro14Pro) variant details
- p.Pro14Pro
- rs376102107
- gnomAD 3-127599353-G-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0863
- CADD 0.80
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available
- Literature evidence available