S13S (p.Ser13Ser) variant of MCM2 (P49736)
S13S (p.Ser13Ser) in MCM2 (P49736) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data, published literature, and structural context.
S13S (p.Ser13Ser) variant details
- p.Ser13Ser
- rs1201891506
- gnomAD 3-127599350-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.226
- CADD 9.80
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available