ClinVar Miner

List of variants in gene GRIN2A reported as uncertain significance for History of neurodevelopmental disorder

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Total variants: 14
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HGVS dbSNP
NM_000833.5(GRIN2A):c.1249G>T (p.Val417Phe)
NM_000833.5(GRIN2A):c.3032G>A (p.Arg1011Gln) rs1163766811
NM_000833.5(GRIN2A):c.3647G>C (p.Ser1216Thr) rs367543134
NM_000833.5(GRIN2A):c.3898A>G (p.Arg1300Gly) rs372353067
NM_000833.5(GRIN2A):c.3909C>G (p.Asp1303Glu)
NM_001134407.3(GRIN2A):c.1738A>G (p.Ser580Gly)
NM_001134407.3(GRIN2A):c.1739G>T (p.Ser580Ile) rs1567332765
NM_001134407.3(GRIN2A):c.2627T>C (p.Ile876Thr) rs199784503
NM_001134407.3(GRIN2A):c.2752C>T (p.Pro918Ser)
NM_001134407.3(GRIN2A):c.3827C>G (p.Ala1276Gly) rs145063086
NM_001134407.3(GRIN2A):c.422C>A (p.Thr141Lys)
NM_001134407.3(GRIN2A):c.547T>A (p.Phe183Ile) rs587780353
NM_001134407.3(GRIN2A):c.890G>A (p.Gly297Asp)
NM_001134407.3(GRIN2A):c.904G>A (p.Ala302Thr)

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