A29V (p.Ala29Val) variant of SDHB (P21912)
A29V (p.Ala29Val) in SDHB (P21912) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact in the context of in PPGL4. The record also includes structural context.
A29V (p.Ala29Val) variant details
- p.Ala29Val
- NCI-TCGA Cosmic COSV1009
- Ensembl rs2101541610
- Variant assessed as somatic; moderate impact.
- in PPGL4
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in PPGL4)
- Structural context available