P36T (p.Pro36Thr) variant of SLC2A1 (P11166)
P36T (p.Pro36Thr) in SLC2A1 (P11166) 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.
P36T (p.Pro36Thr) variant details
- p.Pro36Thr
- rs2525034790
- ClinGen CA339964745
- ClinVar RCV002293805
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available