N110D (p.Asn110Asp) variant of LHCGR (P22888)
N110D (p.Asn110Asp) 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.
N110D (p.Asn110Asp) variant details
- p.Asn110Asp
- NCI-TCGA Cosmic COSV5429
- NCI-TCGA Cosmic COSV9968
- cosmic curated COSV99684
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available