P92Q (p.Pro92Gln) variant of G6PD (P11413)
P92Q (p.Pro92Gln) in G6PD (P11413) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
P92Q (p.Pro92Gln) variant details
- p.Pro92Gln
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available