N41S (p.Asn41Ser) variant of CETP (P11597)
N41S (p.Asn41Ser) 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.
N41S (p.Asn41Ser) variant details
- p.Asn41Ser
- NCI-TCGA Cosmic COSV5236
- cosmic curated COSV52363
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available