I119T (p.Ile119Thr) variant of ABCC9 (O60706)
I119T (p.Ile119Thr) 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.
I119T (p.Ile119Thr) variant details
- p.Ile119Thr
- NCI-TCGA Cosmic COSV5396
- cosmic curated COSV53965
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available