V61D (p.Val61Asp) variant of LHCGR (P22888)
V61D (p.Val61Asp) in LHCGR (P22888) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V61D (p.Val61Asp) variant details
- p.Val61Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available