S37G (p.Ser37Gly) variant of TNNC1 (P63316)
S37G (p.Ser37Gly) in TNNC1 (P63316) 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 structural context.
S37G (p.Ser37Gly) variant details
- p.Ser37Gly
- rs2471444670
- ClinGen CA353169049
- ClinVar RCV003129367
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available