S37R (p.Ser37Arg) variant of SLCO1B1 (Q9Y6L6)
S37R (p.Ser37Arg) in SLCO1B1 (Q9Y6L6) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
S37R (p.Ser37Arg) variant details
- p.Ser37Arg
- NCI-TCGA Cosmic COSV5701
- 1000Genomes rs1349344368
- gnomAD rs1349344368
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.30
- MetaSVM -0.49
- SIFT 0.02
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available