ClinVar Miner

List of variants in gene GRIN1 reported as likely pathogenic for Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant

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Gene type:
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Total variants: 16
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NM_007327.4(GRIN1):c.1667A>G (p.Gln556Arg)
NM_007327.4(GRIN1):c.1847A>G (p.Asn616Ser) rs1564363665
NM_007327.4(GRIN1):c.1858G>A (p.Gly620Arg) rs797045047
NM_007327.4(GRIN1):c.1858G>C (p.Gly620Arg) rs797045047
NM_007327.4(GRIN1):c.1922T>C (p.Met641Thr) rs1588732344
NM_007327.4(GRIN1):c.1939T>C (p.Tyr647His)
NM_007327.4(GRIN1):c.2231G>A (p.Cys744Tyr) rs1554770444
NM_007327.4(GRIN1):c.2381G>A (p.Arg794Gln) rs781053477
NM_007327.4(GRIN1):c.2417C>A (p.Ala806Glu) rs1554770589
NM_007327.4(GRIN1):c.2444G>A (p.Gly815Glu)
NM_007327.4(GRIN1):c.2452A>C (p.Met818Leu) rs1554770628
NM_007327.4(GRIN1):c.2500G>C (p.Glu834Gln) rs1588735834
NM_007327.4(GRIN1):c.2530C>T (p.Arg844Cys) rs1554770667
NM_007327.4(GRIN1):c.352G>A (p.Val118Met) rs1588686286
NM_007327.4(GRIN1):c.448G>A (p.Val150Met)
NM_007327.4(GRIN1):c.679G>C (p.Asp227His)

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