S23L (p.Ser23Leu) variant of CHD2 (O14647)
S23L (p.Ser23Leu) in CHD2 (O14647) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S23L (p.Ser23Leu) variant details
- p.Ser23Leu
- NCI-TCGA Cosmic COSV5912
- cosmic curated COSV59120
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available