ClinVar Miner

List of variants in gene GRIN1 reported by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 39
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HGVS dbSNP
NM_007327.4(GRIN1):c.1005T>C (p.Thr335=) rs145176345
NM_007327.4(GRIN1):c.1012G>A (p.Val338Met) rs140672142
NM_007327.4(GRIN1):c.1044C>T (p.Phe348=) rs143483243
NM_007327.4(GRIN1):c.1198-3C>A rs200368768
NM_007327.4(GRIN1):c.1198-3del rs762423431
NM_007327.4(GRIN1):c.1331C>T (p.Pro444Leu) rs200225692
NM_007327.4(GRIN1):c.1355C>T (p.Pro452Leu) rs1564361971
NM_007327.4(GRIN1):c.1382A>G (p.Asp461Gly) rs955781126
NM_007327.4(GRIN1):c.1513C>T (p.Leu505=) rs139637382
NM_007327.4(GRIN1):c.1548G>A (p.Pro516=) rs75783429
NM_007327.4(GRIN1):c.1584G>A (p.Glu528=) rs116006955
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.1809G>C (p.Leu603=) rs141249927
NM_007327.4(GRIN1):c.1829C>G (p.Ser610Cys) rs1564363645
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.1995G>C (p.Thr665=) rs200127557
NM_007327.4(GRIN1):c.2223G>C (p.Ser741=) rs767848286
NM_007327.4(GRIN1):c.2241G>C (p.Val747=) rs116354349
NM_007327.4(GRIN1):c.2244G>C (p.Thr748=) rs79570612
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.2511C>T (p.Tyr837=) rs1478532319
NM_007327.4(GRIN1):c.2530C>T (p.Arg844Cys) rs1554770667
NM_007327.4(GRIN1):c.344G>A (p.Arg115His)
NM_007327.4(GRIN1):c.467G>A (p.Arg156His) rs762490192
NM_007327.4(GRIN1):c.474C>T (p.Tyr158=) rs1564345160
NM_007327.4(GRIN1):c.525G>A (p.Ala175=) rs77812749
NM_007327.4(GRIN1):c.669C>G (p.Ala223=) rs766714775
NM_007327.4(GRIN1):c.693A>C (p.Val231=) rs201818201
NM_007327.4(GRIN1):c.705C>T (p.Ala235=) rs201343933
NM_007327.4(GRIN1):c.768G>C (p.Gly256=) rs141473515
NM_007327.4(GRIN1):c.789A>G (p.Pro263=) rs6293
NM_007327.4(GRIN1):c.855G>A (p.Val285=) rs1126442
NM_007327.4(GRIN1):c.879C>T (p.His293=) rs746040843
NM_007327.4(GRIN1):c.888C>T (p.Leu296=) rs770334644

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