F36V (p.Phe36Val) variant of ABCC9 (O60706)
F36V (p.Phe36Val) in ABCC9 (O60706) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F36V (p.Phe36Val) variant details
- p.Phe36Val
- NCI-TCGA Cosmic COSV9968
- cosmic curated COSV99684
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available