S9S (p.Ser9Ser) variant of NOD2 (Q9HC29)
S9S (p.Ser9Ser) in NOD2 (Q9HC29) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data, published literature, and structural context.
S9S (p.Ser9Ser) variant details
- p.Ser9Ser
- rs1385280748
- gnomAD 16-50697270-T-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.138
- CADD 6.08
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available