S56I (p.Ser56Ile) variant of CETP (P11597)
S56I (p.Ser56Ile) in CETP (P11597) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S56I (p.Ser56Ile) variant details
- p.Ser56Ile
- NCI-TCGA Cosmic COSV9957
- cosmic curated COSV99570
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available