H368D (p.His368Asp) variant of RPGR (Q92834)
H368D (p.His368Asp) in RPGR (Q92834) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
H368D (p.His368Asp) variant details
- p.His368Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available