P138L (p.Pro138Leu) variant of ABCA3 (Q99758)
P138L (p.Pro138Leu) in ABCA3 (Q99758) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P138L (p.Pro138Leu) variant details
- p.Pro138Leu
- NCI-TCGA Cosmic COSV5705
- cosmic curated COSV57051
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available