Q16R (p.Gln16Arg) variant of HSD3B2 (P26439)
Q16R (p.Gln16Arg) in HSD3B2 (P26439) 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.
Q16R (p.Gln16Arg) variant details
- p.Gln16Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.28
- MetaSVM -0.80
- SIFT 0.18
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available