P19T (p.Pro19Thr) variant of NKX2-1 (Homeobox protein Nkx-2.1)
P19T (p.Pro19Thr) in NKX2-1 (Homeobox protein Nkx-2.1) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not provided. The record also includes population frequency data and structural context.
P19T (p.Pro19Thr) variant details
- p.Pro19Thr
- cosmic curated COSV61388
- ExAC rs776752141
- TOPMed rs776752141
- gnomAD rs776752141
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- UniProt: Uncertain significance
- Population evidence available
- Structural context available