ClinVar Miner

List of variants in gene GRIN1 studied for not specified

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Gene type:
ClinVar version:
Total variants: 92
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HGVS dbSNP
NM_007327.4(GRIN1):c.*9G>A rs1057523226
NM_007327.4(GRIN1):c.-16C>T rs1163701181
NM_007327.4(GRIN1):c.-24G>A rs955395023
NM_007327.4(GRIN1):c.-29G>A rs150851773
NM_007327.4(GRIN1):c.-35C>A rs200150234
NM_007327.4(GRIN1):c.1005T>C (p.Thr335=) rs145176345
NM_007327.4(GRIN1):c.1044C>T (p.Phe348=) rs143483243
NM_007327.4(GRIN1):c.105G>A (p.Thr35=) rs144566508
NM_007327.4(GRIN1):c.1076G>A (p.Arg359His) rs141704101
NM_007327.4(GRIN1):c.1114-5C>T rs1554769139
NM_007327.4(GRIN1):c.1179G>A (p.Gln393=) rs769342069
NM_007327.4(GRIN1):c.1198-6C>T rs1057521991
NM_007327.4(GRIN1):c.1198-7C>T rs202163066
NM_007327.4(GRIN1):c.1339+7GCGCGGGGCAGGGCGCGGG[3] rs761110882
NM_007327.4(GRIN1):c.1431C>T (p.His477=) rs1057522926
NM_007327.4(GRIN1):c.1437G>A (p.Val479=) rs797045604
NM_007327.4(GRIN1):c.1461G>A (p.Gln487=) rs1554769757
NM_007327.4(GRIN1):c.1467+17G>A rs771374825
NM_007327.4(GRIN1):c.1467+19del rs1301624435
NM_007327.4(GRIN1):c.1467+8G>A rs10747050
NM_007327.4(GRIN1):c.1468-17G>C rs750423610
NM_007327.4(GRIN1):c.1497T>C (p.Asn499=) rs748264026
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.1632+14G>A rs200337681
NM_007327.4(GRIN1):c.1701G>A (p.Gly567=) rs1554770070
NM_007327.4(GRIN1):c.1751+13C>T rs770248563
NM_007327.4(GRIN1):c.1809G>C (p.Leu603=) rs141249927
NM_007327.4(GRIN1):c.1864+17C>T rs199730840
NM_007327.4(GRIN1):c.1865-13C>T rs201908310
NM_007327.4(GRIN1):c.1989C>T (p.Arg663=) rs1030685877
NM_007327.4(GRIN1):c.2013+19G>A rs1043866330
NM_007327.4(GRIN1):c.2013+20G>T rs1199869217
NM_007327.4(GRIN1):c.2014-20C>T rs778196740
NM_007327.4(GRIN1):c.2022C>T (p.Asn674=) rs1057522019
NM_007327.4(GRIN1):c.2097G>C (p.Leu699=) rs143865216
NM_007327.4(GRIN1):c.2121G>A (p.Glu707=) rs774389234
NM_007327.4(GRIN1):c.2133C>T (p.Tyr711=) rs760691794
NM_007327.4(GRIN1):c.2171+14G>A rs377411804
NM_007327.4(GRIN1):c.2172-12C>T rs775639156
NM_007327.4(GRIN1):c.2232C>T (p.Cys744=) rs749966599
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.2333+9C>A rs201316377
NM_007327.4(GRIN1):c.2334-18A>T rs185685295
NM_007327.4(GRIN1):c.237C>T (p.Cys79=) rs200529044
NM_007327.4(GRIN1):c.2412C>G (p.Ala804=) rs149053552
NM_007327.4(GRIN1):c.2443+14C>T rs986727477
NM_007327.4(GRIN1):c.2443+15A>G rs201269307
NM_007327.4(GRIN1):c.2444-14G>A rs191352124
NM_007327.4(GRIN1):c.2499C>T (p.Ile833=) rs146086141
NM_007327.4(GRIN1):c.255C>T (p.Ser85=) rs797045605
NM_007327.4(GRIN1):c.258+18C>T rs202160831
NM_007327.4(GRIN1):c.2589+6G>T rs200395927
NM_007327.4(GRIN1):c.2700+11G>C rs199870929
NM_007327.4(GRIN1):c.2700+8G>A rs201887636
NM_007327.4(GRIN1):c.2799C>T (p.Ser933=) rs201012245
NM_007327.4(GRIN1):c.297C>T (p.Asn99=) rs1234541526
NM_007327.4(GRIN1):c.333C>T (p.Ala111=) rs76325634
NM_007327.4(GRIN1):c.351C>A (p.Pro117=) rs772616726
NM_007327.4(GRIN1):c.357G>A (p.Leu119=) rs201475721
NM_007327.4(GRIN1):c.387G>A (p.Ser129=) rs199799811
NM_007327.4(GRIN1):c.387G>C (p.Ser129=) rs199799811
NM_007327.4(GRIN1):c.394-11G>A rs75081117
NM_007327.4(GRIN1):c.394-13C>T rs757225081
NM_007327.4(GRIN1):c.394-19G>A rs371244693
NM_007327.4(GRIN1):c.394-4G>A rs202180269
NM_007327.4(GRIN1):c.426G>A (p.Pro142=) rs201424528
NM_007327.4(GRIN1):c.525G>A (p.Ala175=) rs77812749
NM_007327.4(GRIN1):c.570+10G>A rs200924771
NM_007327.4(GRIN1):c.570+12C>T rs201869639
NM_007327.4(GRIN1):c.570+13G>A rs200081727
NM_007327.4(GRIN1):c.570+16G>A rs201978748
NM_007327.4(GRIN1):c.570+20G>A rs760668899
NM_007327.4(GRIN1):c.571-19A>C rs1554767318
NM_007327.4(GRIN1):c.571-4G>A rs201740054
NM_007327.4(GRIN1):c.614C>T (p.Thr205Met) rs201592328
NM_007327.4(GRIN1):c.630G>A (p.Glu210=) rs1057522916
NM_007327.4(GRIN1):c.63G>A (p.Ala21=) rs759756646
NM_007327.4(GRIN1):c.66C>T (p.Cys22=) rs148688400
NM_007327.4(GRIN1):c.693A>C (p.Val231=) rs201818201
NM_007327.4(GRIN1):c.696C>T (p.Tyr232=) rs200390848
NM_007327.4(GRIN1):c.747C>T (p.Val249=) rs199802957
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.793+12G>A rs200668900
NM_007327.4(GRIN1):c.793+15T>C rs200522831
NM_007327.4(GRIN1):c.855G>A (p.Val285=) rs1126442
NM_007327.4(GRIN1):c.864G>A (p.Val288=) rs770852927
NM_007327.4(GRIN1):c.930C>T (p.Gly310=) rs1057523802
NM_007327.4(GRIN1):c.968+10dup rs777548072

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