P12S (p.Pro12Ser) variant of ABCG8 (Q9H221)
P12S (p.Pro12Ser) 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.
P12S (p.Pro12Ser) variant details
- p.Pro12Ser
- NCI-TCGA Cosmic COSV5321
- cosmic curated COSV53212
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available