S7S (p.Ser7Ser) variant of MCM2 (P49736)
S7S (p.Ser7Ser) in MCM2 (P49736) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data, published literature, and structural context.
S7S (p.Ser7Ser) variant details
- p.Ser7Ser
- rs1207593703
- gnomAD 3-127599332-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.246
- CADD 10.50
- Most common in the Latino/Admixed American population (allele frequency 4.5e-05)
- Structural context available
- Literature evidence available