S37N (p.Ser37Asn) variant of TNNC1 (P63316)
S37N (p.Ser37Asn) in TNNC1 (P63316) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S37N (p.Ser37Asn) variant details
- p.Ser37Asn
- NCI-TCGA Cosmic COSV5176
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available