S146C (p.Ser146Cys) variant of IFT172 (Q9UG01)
S146C (p.Ser146Cys) in IFT172 (Q9UG01) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S146C (p.Ser146Cys) variant details
- p.Ser146Cys
- NCI-TCGA Cosmic COSV5313
- NCI-TCGA Cosmic COSV5314
- cosmic curated COSV53140
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available