V101L (p.Val101Leu) variant of SLC2A2 (P11168)
V101L (p.Val101Leu) in SLC2A2 (P11168) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes structural context.
V101L (p.Val101Leu) variant details
- p.Val101Leu
- 1000Genomes rs1800572
- ESP rs1800572
- ExAC rs1800572
- TOPMed rs1800572
- Benign
- Missense
- EBI: Benign (in dbSNP:rs1800572)
- UniProt: Benign (in dbSNP:rs1800572)
- Structural context available