P39L (p.Pro39Leu) variant of APOL1 (Apolipoprotein L1)
P39L (p.Pro39Leu) in APOL1 (Apolipoprotein L1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P39L (p.Pro39Leu) variant details
- p.Pro39Leu
- NCI-TCGA Cosmic COSV1000
- cosmic curated COSV10004
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available