A19T (p.Ala19Thr) variant of CHD2 (O14647)
A19T (p.Ala19Thr) in CHD2 (O14647) 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.
A19T (p.Ala19Thr) variant details
- p.Ala19Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.48
- MetaSVM -0.46
- SIFT 0.09
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available