P110S (p.Pro110Ser) variant of ADNP (Q9H2P0)
P110S (p.Pro110Ser) in ADNP (Q9H2P0) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of ADNP-related disorder. The record also includes structural context.
P110S (p.Pro110Ser) variant details
- p.Pro110Ser
- rs2515592592
- ClinGen CA408979406
- ClinVar RCV003405875
- Uncertain significance
- ADNP-related disorder
- Missense
- ClinVar: Uncertain significance (ADNP-related disorder)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available