H69Q (p.His69Gln) variant of NKX2-1 (Homeobox protein Nkx-2.1)
H69Q (p.His69Gln) in NKX2-1 (Homeobox protein Nkx-2.1) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes population frequency data and structural context.
H69Q (p.His69Gln) variant details
- p.His69Gln
- TOPMed rs1312450089
- gnomAD rs1312450089
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Population evidence available
- Structural context available