D68G (p.Asp68Gly) variant of DNMT3A (Q9Y6K1)
D68G (p.Asp68Gly) in DNMT3A (Q9Y6K1) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
D68G (p.Asp68Gly) variant details
- p.Asp68Gly
- rs2465823019
- ClinGen CA346084157
- ClinVar RCV003223015
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available