R77G (p.Arg77Gly) variant of SPTBN2 (O15020)
R77G (p.Arg77Gly) in SPTBN2 (O15020) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided.
R77G (p.Arg77Gly) variant details
- p.Arg77Gly
- rs200956071
- ClinVar RCV004592418
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance