S29F (p.Ser29Phe) variant of ABCG8 (Q9H221)
S29F (p.Ser29Phe) in ABCG8 (Q9H221) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S29F (p.Ser29Phe) variant details
- p.Ser29Phe
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available