ClinVar Miner

List of variants in gene GRIN1 studied for Inborn genetic diseases

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Total variants: 11
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HGVS dbSNP
NM_007327.4(GRIN1):c.1382A>G (p.Asp461Gly) rs955781126
NM_007327.4(GRIN1):c.1643G>A (p.Arg548Gln) rs1554770044
NM_007327.4(GRIN1):c.1645A>C (p.Ser549Arg) rs1554770046
NM_007327.4(GRIN1):c.1852G>C (p.Gly618Arg)
NM_007327.4(GRIN1):c.1858G>C (p.Gly620Arg) rs797045047
NM_007327.4(GRIN1):c.1958C>G (p.Ala653Gly) rs1554770258
NM_007327.4(GRIN1):c.1979C>T (p.Pro660Leu) rs1328780843
NM_007327.4(GRIN1):c.2420C>T (p.Thr807Ile) rs1554770590
NM_007327.4(GRIN1):c.2443G>A (p.Gly815Arg) rs797044925
NM_007327.4(GRIN1):c.2530C>T (p.Arg844Cys) rs1554770667
NM_007327.4(GRIN1):c.344G>A (p.Arg115His)

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