E53D (p.Glu53Asp) variant of F9 (Coagulation factor IX)
E53D (p.Glu53Asp) in F9 (Coagulation factor IX) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact in the context of in HEMB. The record also includes structural context.
E53D (p.Glu53Asp) variant details
- p.Glu53Asp
- cosmic curated COSV10804
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- in HEMB
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in HEMB)
- Structural context available