Q2L (p.Gln2Leu) variant of SOS2 (Son of sevenless homolog 2)
Q2L (p.Gln2Leu) 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 Cardiovascular phenotype. The record also includes structural context.
Q2L (p.Gln2Leu) variant details
- p.Gln2Leu
- rs2503347322
- ClinGen CA389657731
- ClinVar RCV004517240
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available