L436H (p.Leu436His) variant of SLC6A1 (P30531)
L436H (p.Leu436His) in SLC6A1 (P30531) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely pathogenic in the context of Epilepsy with myoclonic atonic seizures. The available variant effect predictions contribute to a CATVariant prioritization score of 0.86 / 1. The record also includes published literature and structural context.
L436H (p.Leu436His) variant details
- p.Leu436His
- rs2124932154
- ClinGen CA351791292
- ClinVar RCV003444243
- Ensembl rs2124932154
- Likely pathogenic
- Epilepsy with myoclonic atonic seizures
- Missense
- Variant Prioritization Score for Impact Estimate 0.858
- AlphaMissense 0.98
- MetaLR 0.81
- MetaSVM 0.93
- PolyPhen-2 1.00
- SIFT 0.00
- EVE 0.81
- ClinVar: Likely pathogenic (Epilepsy with myoclonic atonic seizures)
- EBI: Likely pathogenic
- UniProt: Likely pathogenic
- Structural context available
- Cited in: SLC6A1-Related Neurodevelopmental Disorder. (PMID 36780407)