S35S (p.Ser35Ser) variant of CHD2 (O14647)
S35S (p.Ser35Ser) in CHD2 (O14647) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data, published literature, and structural context.
S35S (p.Ser35Ser) variant details
- p.Ser35Ser
- rs1279999895
- gnomAD 15-92924363-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.432
- CADD 13.20
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available