A2P (p.Ala2Pro) variant of SDHB (P21912)
A2P (p.Ala2Pro) in SDHB (P21912) 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.
A2P (p.Ala2Pro) variant details
- p.Ala2Pro
- NCI-TCGA Cosmic COSV6496
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available