K77Q (p.Lys77Gln) variant of LHCGR (P22888)
K77Q (p.Lys77Gln) 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.
K77Q (p.Lys77Gln) variant details
- p.Lys77Gln
- NCI-TCGA Cosmic COSV5430
- cosmic curated COSV54300
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available