L53Q (p.Leu53Gln) variant of CYP11B1 (P15538)
L53Q (p.Leu53Gln) in CYP11B1 (P15538) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
L53Q (p.Leu53Gln) variant details
- p.Leu53Gln
- NCI-TCGA Cosmic COSV5283
- cosmic curated COSV52830
- Ensembl rs1586561962
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available