G96A (p.Gly96Ala) variant of TNFRSF9 (Q07011)
G96A (p.Gly96Ala) in TNFRSF9 (Q07011) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes structural context.
G96A (p.Gly96Ala) variant details
- p.Gly96Ala
- Ensembl rs1639851645
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available