N176K (p.Asn176Lys) variant of RPGR (Q92834)
N176K (p.Asn176Lys) in RPGR (Q92834) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
N176K (p.Asn176Lys) variant details
- p.Asn176Lys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available