P9L (p.Pro9Leu) variant of ABCG5 (Q9H222)
P9L (p.Pro9Leu) in ABCG5 (Q9H222) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
P9L (p.Pro9Leu) variant details
- p.Pro9Leu
- NCI-TCGA Cosmic COSV5321
- cosmic curated COSV53213
- Variant assessed as somatic; moderate impact.
- Missense
- SIFT 0.21
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available