T67M (p.Thr67Met) variant of PPP2R5D (Q14738)
T67M (p.Thr67Met) in PPP2R5D (Q14738) 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.
T67M (p.Thr67Met) variant details
- p.Thr67Met
- rs2532471813
- ClinGen CA364179688
- ClinVar RCV003691309
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available