P16T (p.Pro16Thr) variant of SLC2A4 (P14672)
P16T (p.Pro16Thr) in SLC2A4 (P14672) is a missense change. The record also includes structural context.
P16T (p.Pro16Thr) variant details
- p.Pro16Thr
- TOPMed rs1170001111
- gnomAD rs1170001111
- Missense
- Structural context available