R18S (p.Arg18Ser) variant of SDHAF2 (Q9NX18)
R18S (p.Arg18Ser) 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.
R18S (p.Arg18Ser) variant details
- p.Arg18Ser
- NCI-TCGA TCGA novel
- gnomAD rs1590764725
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available