ClinVar Miner

List of variants in gene GRIN1 reported as likely pathogenic

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Gene type:
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Total variants: 33
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HGVS dbSNP
NM_007327.4(GRIN1):c.1595C>A (p.Pro532His) rs1064795158
NM_007327.4(GRIN1):c.1607A>G (p.Gln536Arg) rs1064795337
NM_007327.4(GRIN1):c.1667A>G (p.Gln556Arg)
NM_007327.4(GRIN1):c.1670C>T (p.Pro557Leu) rs878853143
NM_007327.4(GRIN1):c.1744C>A (p.Arg582Ser)
NM_007327.4(GRIN1):c.1847A>G (p.Asn616Ser) rs1564363665
NM_007327.4(GRIN1):c.1852G>C (p.Gly618Arg)
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.1910C>T (p.Ala637Val) rs1554770221
NM_007327.4(GRIN1):c.1922T>C (p.Met641Thr) rs1588732344
NM_007327.4(GRIN1):c.1924A>C (p.Ile642Leu) rs1064795455
NM_007327.4(GRIN1):c.1939T>C (p.Tyr647His)
NM_007327.4(GRIN1):c.1949A>T (p.Asn650Ile) rs1131691590
NM_007327.4(GRIN1):c.1974C>G (p.Asp658Glu) rs1064795712
NM_007327.4(GRIN1):c.1979C>T (p.Pro660Leu) rs1328780843
NM_007327.4(GRIN1):c.2008C>A (p.Pro670Thr) rs1057520055
NM_007327.4(GRIN1):c.2021A>T (p.Asn674Ile)
NM_007327.4(GRIN1):c.2062T>C (p.Ser688Pro) rs1131691576
NM_007327.4(GRIN1):c.2063C>A (p.Ser688Tyr)
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.2441C>A (p.Ala814Asp) rs1131691870
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.2531G>T (p.Arg844Leu) rs1564365418
NM_007327.4(GRIN1):c.329C>T (p.Thr110Ile) rs1064794987
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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