A101D (p.Ala101Asp) variant of MCCC1 (Q96RQ3)
A101D (p.Ala101Asp) in MCCC1 (Q96RQ3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A101D (p.Ala101Asp) variant details
- p.Ala101Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available