G97D (p.Gly97Asp) variant of NPHS2 (Podocin)
G97D (p.Gly97Asp) in NPHS2 (Podocin) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance in the context of in NPHS2. The record also includes structural context.
G97D (p.Gly97Asp) variant details
- p.Gly97Asp
- NCI-TCGA TCGA novel
- TOPMed rs1674274310
- Uncertain significance
- in NPHS2
- Missense
- EBI: uncertain significance (in NPHS2)
- UniProt: Uncertain significance (in NPHS2)
- Structural context available