D39H (p.Asp39His) variant of PRMT5 (O14744)
D39H (p.Asp39His) in PRMT5 (O14744) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D39H (p.Asp39His) variant details
- p.Asp39His
- NCI-TCGA Cosmic COSV5354
- cosmic curated COSV53546
- NCI-TCGA Cosmic COSV9936
- Ensembl rs2139254728
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available