I14T (p.Ile14Thr) variant of CHM (P24386)
I14T (p.Ile14Thr) in CHM (P24386) 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.
I14T (p.Ile14Thr) variant details
- p.Ile14Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.53
- MetaSVM 0.14
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available