ClinVar Miner

List of variants in gene GRIN1 reported as likely benign for not specified

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_007327.4(GRIN1):c.1467+8G>A rs10747050 0.95319
NM_007327.4(GRIN1):c.789A>G (p.Pro263=) rs6293 0.23665
NM_007327.4(GRIN1):c.855G>A (p.Val285=) rs1126442 0.23587
NM_007327.4(GRIN1):c.2241G>C (p.Val747=) rs116354349 0.01638
NM_007327.4(GRIN1):c.2244G>C (p.Thr748=) rs79570612 0.01637
NM_007327.4(GRIN1):c.1584G>A (p.Glu528=) rs116006955 0.00510
NM_007327.4(GRIN1):c.258+18C>T rs202160831 0.00130
NM_007327.4(GRIN1):c.570+10G>A rs200924771 0.00078
NM_007327.4(GRIN1):c.1632+14G>A rs200337681 0.00065
NM_007327.4(GRIN1):c.2799C>T (p.Ser933=) rs201012245 0.00026
NM_007327.4(GRIN1):c.2444-14G>A rs191352124 0.00024
NM_007327.4(GRIN1):c.1005T>C (p.Thr335=) rs145176345 0.00023
NM_007327.4(GRIN1):c.394-19G>A rs371244693 0.00021
NM_007327.4(GRIN1):c.793+15T>C rs200522831 0.00011
NM_007327.4(GRIN1):c.2333+9C>A rs201316377 0.00006
NM_007327.4(GRIN1):c.570+13G>A rs200081727 0.00005
NM_007327.4(GRIN1):c.-24G>A rs955395023 0.00004
NM_007327.4(GRIN1):c.1076G>A (p.Arg359His) rs141704101 0.00004
NM_007327.4(GRIN1):c.1179G>A (p.Gln393=) rs769342069 0.00004
NM_007327.4(GRIN1):c.570+12C>T rs201869639 0.00004
NM_007327.4(GRIN1):c.2700+11G>C rs199870929 0.00003
NM_007327.4(GRIN1):c.351C>A (p.Pro117=) rs772616726 0.00003
NM_007327.4(GRIN1):c.426G>A (p.Pro142=) rs201424528 0.00003
NM_007327.4(GRIN1):c.793+12G>A rs200668900 0.00003
NM_007327.4(GRIN1):c.2013+19G>A rs1043866330 0.00002
NM_007327.4(GRIN1):c.630G>A (p.Glu210=) rs1057522916 0.00002
NM_007327.4(GRIN1):c.1467+17G>A rs771374825 0.00001
NM_007327.4(GRIN1):c.1751+13C>T rs770248563 0.00001
NM_007327.4(GRIN1):c.2013+20G>T rs1199869217 0.00001
NM_007327.4(GRIN1):c.2121G>A (p.Glu707=) rs774389234 0.00001
NM_007327.4(GRIN1):c.2171+14G>A rs377411804 0.00001
NM_007327.4(GRIN1):c.2334-18A>T rs185685295 0.00001
NM_007327.4(GRIN1):c.237C>T (p.Cys79=) rs200529044 0.00001
NM_007327.4(GRIN1):c.2443+14C>T rs986727477 0.00001
NM_007327.4(GRIN1):c.357G>A (p.Leu119=) rs201475721 0.00001
NM_007327.4(GRIN1):c.394-13C>T rs757225081 0.00001
NM_007327.4(GRIN1):c.747C>T (p.Val249=) rs199802957 0.00001
NM_007327.4(GRIN1):c.*9G>A rs1057523226
NM_007327.4(GRIN1):c.-16C>T rs1163701181
NM_007327.4(GRIN1):c.-29G>A rs150851773
NM_007327.4(GRIN1):c.1114-5C>T rs1554769139
NM_007327.4(GRIN1):c.1198-6C>T rs1057521991
NM_007327.4(GRIN1):c.1431C>T (p.His477=) rs1057522926
NM_007327.4(GRIN1):c.1461G>A (p.Gln487=) rs1554769757
NM_007327.4(GRIN1):c.1467+19del rs1301624435
NM_007327.4(GRIN1):c.1468-17G>C rs750423610
NM_007327.4(GRIN1):c.1497T>C (p.Asn499=) rs748264026
NM_007327.4(GRIN1):c.1701G>A (p.Gly567=) rs1554770070
NM_007327.4(GRIN1):c.1989C>T (p.Arg663=) rs1030685877
NM_007327.4(GRIN1):c.2014-20C>T rs778196740
NM_007327.4(GRIN1):c.2022C>T (p.Asn674=) rs1057522019
NM_007327.4(GRIN1):c.2133C>T (p.Tyr711=) rs760691794
NM_007327.4(GRIN1):c.2172-12C>T rs775639156
NM_007327.4(GRIN1):c.2443+15A>G rs201269307
NM_007327.4(GRIN1):c.2700+8G>A rs201887636
NM_007327.4(GRIN1):c.333C>T (p.Ala111=) rs76325634
NM_007327.4(GRIN1):c.555G>A (p.Glu185=)
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.63G>A (p.Ala21=) rs759756646
NM_007327.4(GRIN1):c.930C>T (p.Gly310=) rs1057523802
NM_007327.4(GRIN1):c.968+10dup rs777548072

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