P136S (p.Pro136Ser) variant of HSD17B3 (P37058)
P136S (p.Pro136Ser) in HSD17B3 (P37058) 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.
P136S (p.Pro136Ser) variant details
- p.Pro136Ser
- NCI-TCGA Cosmic COSV6455
- cosmic curated COSV64557
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.42
- MetaSVM -0.57
- SIFT 0.18
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available