R17P (p.Arg17Pro) variant of SDHD (O14521)
R17P (p.Arg17Pro) in SDHD (O14521) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R17P (p.Arg17Pro) variant details
- p.Arg17Pro
- NCI-TCGA Cosmic COSV5477
- cosmic curated COSV54778
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available