C27T (p.Cys27Thr) variant of NPC2 (P61916)
C27T (p.Cys27Thr) in NPC2 (P61916) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
C27T (p.Cys27Thr) variant details
- p.Cys27Thr
- NCI-TCGA Cosmic COSV5314
- cosmic curated COSV53143
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available