S14S (p.Ser14Ser) variant of CHD2 (O14647)
S14S (p.Ser14Ser) in CHD2 (O14647) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data, published literature, and structural context.
S14S (p.Ser14Ser) variant details
- p.Ser14Ser
- rs1163731878
- gnomAD 15-92901279-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.418
- CADD 13.70
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available
- Literature evidence available