T77N (p.Thr77Asn) variant of SPTA1 (P02549)
T77N (p.Thr77Asn) in SPTA1 (P02549) is a missense change. Clinical records from ClinVar and UniProt describe it as conflicting interpretations in the context of not specified; not provided.
T77N (p.Thr77Asn) variant details
- p.Thr77Asn
- ESP rs372828197
- ExAC rs372828197
- TOPMed rs372828197
- gnomAD rs372828197
- Conflicting interpretations
- not specified; not provided
- Missense
- ClinVar: Conflicting classifications of pathogenicity (not specified; not provided)
- UniProt: Conflicting interpretations