S23P (p.Ser23Pro) variant of CHD2 (O14647)
S23P (p.Ser23Pro) 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.
S23P (p.Ser23Pro) variant details
- p.Ser23Pro
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.73
- MetaSVM 0.59
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available