R27T (p.Arg27Thr) variant of SDHD (O14521)
R27T (p.Arg27Thr) in SDHD (O14521) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
R27T (p.Arg27Thr) variant details
- p.Arg27Thr
- NCI-TCGA Cosmic COSV5477
- cosmic curated COSV54778
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available