ClinVar Miner

List of variants in gene GRIN1 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 121
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HGVS dbSNP gnomAD frequency
NM_007327.4(GRIN1):c.1468-219_1468-218del rs1412493529 0.05931
NM_007327.4(GRIN1):c.259-203G>A rs78889075 0.03332
NM_007327.4(GRIN1):c.394-32A>G rs200424067 0.00935
NM_007327.4(GRIN1):c.1340-18_1340-17insGTA rs199804460 0.00721
NM_007327.4(GRIN1):c.672-147C>T rs117627988 0.00520
NM_007327.4(GRIN1):c.672-148G>A rs117281178 0.00520
NM_007327.4(GRIN1):c.393+156G>A rs115185273 0.00423
NM_007327.4(GRIN1):c.394-38G>A rs201269024 0.00409
NM_007327.4(GRIN1):c.394-267A>G rs13299928 0.00388
NM_007327.4(GRIN1):c.394-215G>A rs542878283 0.00347
NM_007327.4(GRIN1):c.394-307G>A rs537004900 0.00276
NM_007327.4(GRIN1):c.2333+56C>T rs569694173 0.00235
NM_007327.4(GRIN1):c.1198-176T>C rs189008213 0.00227
NM_007327.4(GRIN1):c.672-215C>T rs144887370 0.00226
NM_007327.4(GRIN1):c.671+168G>A rs564114356 0.00213
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.1864+17C>T rs199730840 0.00039
NM_007327.4(GRIN1):c.2412C>G (p.Ala804=) rs149053552 0.00039
NM_007327.4(GRIN1):c.2799C>T (p.Ser933=) rs201012245 0.00026
NM_007327.4(GRIN1):c.693A>C (p.Val231=) rs201818201 0.00025
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.105G>A (p.Thr35=) rs144566508 0.00021
NM_007327.4(GRIN1):c.394-19G>A rs371244693 0.00021
NM_007327.4(GRIN1):c.2214C>T (p.Phe738=) rs367543116 0.00018
NM_007327.4(GRIN1):c.2097G>C (p.Leu699=) rs143865216 0.00016
NM_007327.4(GRIN1):c.633G>A (p.Ala211=) rs150405897 0.00016
NM_007327.4(GRIN1):c.1012G>A (p.Val338Met) rs140672142 0.00015
NM_007327.4(GRIN1):c.403C>T (p.Leu135=) rs200400213 0.00015
NM_007327.4(GRIN1):c.1340C>A (p.Pro447His) rs587780348 0.00014
NM_007327.4(GRIN1):c.793+15T>C rs200522831 0.00011
NM_007327.4(GRIN1):c.1865-13C>T rs201908310 0.00009
NM_007327.4(GRIN1):c.1995G>C (p.Thr665=) rs200127557 0.00009
NM_007327.4(GRIN1):c.513C>T (p.His171=) rs144687877 0.00009
NM_007327.4(GRIN1):c.610G>A (p.Val204Met) rs140422926 0.00009
NM_007327.4(GRIN1):c.66C>T (p.Cys22=) rs148688400 0.00009
NM_007327.4(GRIN1):c.2328C>T (p.Ile776=) rs200088954 0.00008
NM_007327.4(GRIN1):c.1198-7C>T rs202163066 0.00006
NM_007327.4(GRIN1):c.2333+9C>A rs201316377 0.00006
NM_007327.4(GRIN1):c.696C>T (p.Tyr232=) rs200390848 0.00006
NM_007327.4(GRIN1):c.467G>A (p.Arg156His) rs762490192 0.00005
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.159C>T (p.His53=) rs147818786 0.00004
NM_007327.4(GRIN1):c.2499C>T (p.Ile833=) rs146086141 0.00004
NM_007327.4(GRIN1):c.507C>T (p.Asp169=) rs199720207 0.00004
NM_007327.4(GRIN1):c.570+12C>T rs201869639 0.00004
NM_007327.4(GRIN1):c.*8C>T rs200191444 0.00003
NM_007327.4(GRIN1):c.1011C>A (p.Arg337=) rs138950430 0.00003
NM_007327.4(GRIN1):c.1045G>T (p.Ala349Ser) rs148008303 0.00003
NM_007327.4(GRIN1):c.2589+6G>T rs200395927 0.00003
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.387G>C (p.Ser129=) rs199799811 0.00003
NM_007327.4(GRIN1):c.426G>A (p.Pro142=) rs201424528 0.00003
NM_007327.4(GRIN1):c.614C>T (p.Thr205Met) rs201592328 0.00003
NM_007327.4(GRIN1):c.793+12G>A rs200668900 0.00003
NM_007327.4(GRIN1):c.1776C>T (p.Asn592=) rs369596145 0.00002
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.*14C>T rs1225218254 0.00001
NM_007327.4(GRIN1):c.1149C>T (p.Gly383=) rs138398771 0.00001
NM_007327.4(GRIN1):c.1467+17G>A rs771374825 0.00001
NM_007327.4(GRIN1):c.152A>G (p.Lys51Arg) rs767000671 0.00001
NM_007327.4(GRIN1):c.1751+13C>T rs770248563 0.00001
NM_007327.4(GRIN1):c.1806C>T (p.Thr602=) rs1039715252 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.258+19G>A rs1447155507 0.00001
NM_007327.4(GRIN1):c.297C>T (p.Asn99=) rs1234541526 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.822C>T (p.Gly274=) rs753815068 0.00001
NM_007327.4(GRIN1):c.864G>A (p.Val288=) rs770852927 0.00001
NM_007327.4(GRIN1):c.*9G>A rs1057523226
NM_007327.4(GRIN1):c.-16C>T rs1163701181
NM_007327.4(GRIN1):c.-288CCG[5] rs763024426
NM_007327.4(GRIN1):c.-29G>A rs150851773
NM_007327.4(GRIN1):c.1114-5C>T rs1554769139
NM_007327.4(GRIN1):c.1198-231C>G rs186486522
NM_007327.4(GRIN1):c.1198-231dup rs571318041
NM_007327.4(GRIN1):c.1198-6C>T rs1057521991
NM_007327.4(GRIN1):c.1340-17C>A rs555815195
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.1467+223T>C rs928746317
NM_007327.4(GRIN1):c.1468-17G>C rs750423610
NM_007327.4(GRIN1):c.1497T>C (p.Asn499=) rs748264026
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.2232C>T (p.Cys744=) rs749966599
NM_007327.4(GRIN1):c.2443+15A>G rs201269307
NM_007327.4(GRIN1):c.2481G>A (p.Gly827=) rs200393867
NM_007327.4(GRIN1):c.2562C>T (p.Ala854=) rs773955784
NM_007327.4(GRIN1):c.2700+8G>A rs201887636
NM_007327.4(GRIN1):c.333C>T (p.Ala111=) rs76325634
NM_007327.4(GRIN1):c.387G>A (p.Ser129=) rs199799811
NM_007327.4(GRIN1):c.394-22_394-20delinsACT rs1588694679
NM_007327.4(GRIN1):c.394-247_394-188del rs1564344525
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.78C>T (p.Ile26=) rs2131186471
NM_007327.4(GRIN1):c.930C>T (p.Gly310=) rs1057523802
NM_007327.4(GRIN1):c.968+10dup rs777548072
NM_007327.4(GRIN1):c.968+218G>A rs143877162

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