M641I (p.Met641Ile) variant of GRIN1 (Q05586)
M641I (p.Met641Ile) in GRIN1 (Q05586) is a missense change. Clinical records from ClinVar and UniProt describe it as likely pathogenic in the context of Neurodevelopmental disorder with or without hyperkinetic movements and seizures. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes published literature and structural context.
M641I (p.Met641Ile) variant details
- p.Met641Ile
- rs1060500046
- Likely pathogenic
- Neurodevelopmental disorder with or without hyperkinetic movements and seizures
- Missense
- Variant Prioritization Score for Impact Estimate 0.464
- AlphaMissense 1.00
- MetaLR 0.30
- MetaSVM -0.39
- PolyPhen-2 0.99
- SIFT 0.01
- EVE 0.53
- ClinVar: Likely pathogenic (Neurodevelopmental disorder with or without hyperkinetic movemen)
- UniProt: Likely pathogenic (in NDHMSD)
- Structural context available
- Cited in: GRIN1 mutations cause encephalopathy with infantile-onset epilepsy, and hyperkinetic and stereotyped movement disorders. (PMID 25864721)
- Cited in: De novo GRIN variants in M3 helix associated with neurological disorders control channel gating of NMDA receptor. (PMID 38538865)