S20= variant of CHD2 (O14647)
S20= in CHD2 (O14647) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; low impact. The record also includes structural context.
S20= variant details
- NCI-TCGA TCGA novel
- Variant assessed as somatic; low impact.
- Missense
- UniProt: Variant assessed as somatic; low impact.
- Structural context available