S77G (p.Ser77Gly) variant of MTOR (P42345)
S77G (p.Ser77Gly) in MTOR (P42345) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes variant effect predictions and structural context.
S77G (p.Ser77Gly) variant details
- p.Ser77Gly
- rs2100984049
- ClinGen CA338404778
- ClinVar RCV001767572
- Ensembl rs2100984049
- Uncertain significance
- not provided
- Missense
- MutPred 0.24
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available