P29S (p.Pro29Ser) variant of SDHC (Q99643)
P29S (p.Pro29Ser) in SDHC (Q99643) 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 variant effect predictions and structural context.
P29S (p.Pro29Ser) variant details
- p.Pro29Ser
- NCI-TCGA Cosmic COSV6136
- cosmic curated COSV61369
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- MetaLR 0.90
- MetaSVM 0.92
- SIFT 0.06
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available