S77N (p.Ser77Asn) variant of ADNP (Q9H2P0)
S77N (p.Ser77Asn) in ADNP (Q9H2P0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.76 / 1. The record also includes population frequency data and structural context.
S77N (p.Ser77Asn) variant details
- p.Ser77Asn
- gnomAD rs1981180832
- Missense
- Variant Prioritization Score for Impact Estimate 0.756
- CADD 24.30
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available