ClinVar Miner

List of variants in gene GRIN2A reported as likely pathogenic for Epilepsy, focal, with speech disorder and with or without mental retardation

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Total variants: 8
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NM_000833.5(GRIN2A):c.1936A>G (p.Thr646Ala) rs1555492758
NM_001134407.3(GRIN2A):c.1553G>A (p.Arg518His) rs397518470
NM_001134407.3(GRIN2A):c.1673G>C (p.Trp558Ser) rs1555493585
NM_001134407.3(GRIN2A):c.2069C>T (p.Thr690Met) rs1445802934
NM_001134407.3(GRIN2A):c.2452G>A (p.Ala818Thr) rs1555483699
NM_001134407.3(GRIN2A):c.2453C>A (p.Ala818Glu) rs751455326
NM_001134407.3(GRIN2A):c.292C>T (p.Leu98Phe)
NM_001134407.3(GRIN2A):c.4375A>G (p.Ser1459Gly) rs869312681

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