S4P (p.Ser4Pro) variant of SDHAF2 (Q9NX18)
S4P (p.Ser4Pro) in SDHAF2 (Q9NX18) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary pheochromocytoma and paraganglioma. The record also includes structural context.
S4P (p.Ser4Pro) variant details
- p.Ser4Pro
- NCI-TCGA Cosmic COSV5709
- cosmic curated COSV57099
- Uncertain significance
- Hereditary pheochromocytoma and paraganglioma
- Missense
- ClinVar: Uncertain significance (Hereditary pheochromocytoma and paraganglioma)
- UniProt: Uncertain significance
- Structural context available