S37S (p.Ser37Ser) variant of CHD2 (O14647)
S37S (p.Ser37Ser) in CHD2 (O14647) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
S37S (p.Ser37Ser) variant details
- p.Ser37Ser
- rs371078680
- gnomAD 15-92924369-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.154
- CADD 10.40
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available