D108N (p.Asp108Asn) variant of SOS2 (Son of sevenless homolog 2)
D108N (p.Asp108Asn) in SOS2 (Son of sevenless homolog 2) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of SOS2-related disorder; not provided. The record also includes structural context.
D108N (p.Asp108Asn) variant details
- p.Asp108Asn
- rs1566477432
- ClinGen CA389649875
- ClinVar RCV000681069
- ClinVar RCV003392517
- Uncertain significance
- SOS2-related disorder; not provided
- Missense
- ClinVar: Uncertain significance (SOS2-related disorder; not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available