A12P (p.Ala12Pro) variant of HSPG2 (P98160)
A12P (p.Ala12Pro) in HSPG2 (P98160) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance.
A12P (p.Ala12Pro) variant details
- p.Ala12Pro
- 1000Genomes rs529434165
- TOPMed rs529434165
- gnomAD rs529434165
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance