Q82D (p.Gln82Asp) variant of LHCGR (P22888)
Q82D (p.Gln82Asp) in LHCGR (P22888) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
Q82D (p.Gln82Asp) variant details
- p.Gln82Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available