P36R (p.Pro36Arg) variant of SLC2A1 (P11166)
P36R (p.Pro36Arg) in SLC2A1 (P11166) is a missense change. Clinical records from ClinVar and UniProt describe it as likely pathogenic in the context of Seizure. The record also includes structural context.
P36R (p.Pro36Arg) variant details
- p.Pro36Arg
- NCI-TCGA Cosmic COSV6528
- Likely pathogenic
- Seizure
- Missense
- ClinVar: Likely pathogenic (Seizure)
- UniProt: Likely pathogenic
- Structural context available