S47A (p.Ser47Ala) variant of TTN (Titin)
S47A (p.Ser47Ala) in TTN (Titin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
S47A (p.Ser47Ala) variant details
- p.Ser47Ala
- NCI-TCGA Cosmic COSV5988
- cosmic curated COSV59886
- NCI-TCGA Cosmic COSV6002
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.