P40S (p.Pro40Ser) variant of SDHAF2 (Q9NX18)
P40S (p.Pro40Ser) in SDHAF2 (Q9NX18) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P40S (p.Pro40Ser) variant details
- p.Pro40Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available