ClinVar Miner

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

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 126
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HGVS dbSNP
NC_000009.11:g.(?_140033939)_(140034216_?)dup
NC_000009.11:g.(?_140059618)_(140062314_?)dup
NM_007327.4(GRIN1):c.1005T>C (p.Thr335=) rs145176345
NM_007327.4(GRIN1):c.1011C>A (p.Arg337=) rs138950430
NM_007327.4(GRIN1):c.1012G>A (p.Val338Met) rs140672142
NM_007327.4(GRIN1):c.1012G>T (p.Val338Leu)
NM_007327.4(GRIN1):c.1045G>T (p.Ala349Ser) rs148008303
NM_007327.4(GRIN1):c.105G>A (p.Thr35=) rs144566508
NM_007327.4(GRIN1):c.1114-8A>G rs779390664
NM_007327.4(GRIN1):c.1114-8dup
NM_007327.4(GRIN1):c.1197+7G>A rs1588721709
NM_007327.4(GRIN1):c.1197+8C>T
NM_007327.4(GRIN1):c.1206G>A (p.Thr402=) rs548201762
NM_007327.4(GRIN1):c.1245G>A (p.Leu415=) rs527709893
NM_007327.4(GRIN1):c.1254G>A (p.Gly418=) rs1003725607
NM_007327.4(GRIN1):c.1257A>G (p.Thr419=) rs201557285
NM_007327.4(GRIN1):c.1263G>A (p.Lys421=)
NM_007327.4(GRIN1):c.1299G>C (p.Lys433Asn)
NM_007327.4(GRIN1):c.1331C>T (p.Pro444Leu) rs200225692
NM_007327.4(GRIN1):c.1339+9G>T rs1588727336
NM_007327.4(GRIN1):c.1340-1G>T
NM_007327.4(GRIN1):c.1344C>T (p.Arg448=) rs200574152
NM_007327.4(GRIN1):c.1398G>A (p.Leu466=)
NM_007327.4(GRIN1):c.1422C>T (p.Tyr474=)
NM_007327.4(GRIN1):c.1431C>T (p.His477=) rs1057522926
NM_007327.4(GRIN1):c.1440A>G (p.Ala480=) rs1439433425
NM_007327.4(GRIN1):c.1449G>A (p.Lys483=) rs778957098
NM_007327.4(GRIN1):c.1467+7_1467+14del
NM_007327.4(GRIN1):c.1468-10C>T rs1226232806
NM_007327.4(GRIN1):c.1488G>A (p.Lys496=)
NM_007327.4(GRIN1):c.1500G>C (p.Gly500=)
NM_007327.4(GRIN1):c.152A>G (p.Lys51Arg) rs767000671
NM_007327.4(GRIN1):c.1572G>T (p.Ala524=)
NM_007327.4(GRIN1):c.1575G>A (p.Gln525=)
NM_007327.4(GRIN1):c.159C>T (p.His53=) rs147818786
NM_007327.4(GRIN1):c.1621C>T (p.Leu541=)
NM_007327.4(GRIN1):c.1641C>T (p.Pro547=)
NM_007327.4(GRIN1):c.1650G>A (p.Thr550=) rs1588731007
NM_007327.4(GRIN1):c.1650G>T (p.Thr550=)
NM_007327.4(GRIN1):c.1671G>C (p.Pro557=) rs1348812038
NM_007327.4(GRIN1):c.1751+8C>G
NM_007327.4(GRIN1):c.1776C>T (p.Asn592=) rs369596145
NM_007327.4(GRIN1):c.180C>T (p.Leu60=)
NM_007327.4(GRIN1):c.1818C>T (p.Ala606=)
NM_007327.4(GRIN1):c.1830C>T (p.Ser610=)
NM_007327.4(GRIN1):c.192C>T (p.Ser64=)
NM_007327.4(GRIN1):c.1995G>C (p.Thr665=) rs200127557
NM_007327.4(GRIN1):c.2052G>A (p.Val684=)
NM_007327.4(GRIN1):c.2097G>C (p.Leu699=) rs143865216
NM_007327.4(GRIN1):c.2171+10G>C
NM_007327.4(GRIN1):c.2178G>A (p.Leu726=)
NM_007327.4(GRIN1):c.2214C>T (p.Phe738=) rs367543116
NM_007327.4(GRIN1):c.2217G>A (p.Glu739=)
NM_007327.4(GRIN1):c.2223G>C (p.Ser741=) rs767848286
NM_007327.4(GRIN1):c.2232C>T (p.Cys744=) rs749966599
NM_007327.4(GRIN1):c.2235C>T (p.Asp745=) rs200518957
NM_007327.4(GRIN1):c.2253G>A (p.Glu751=) rs1219774135
NM_007327.4(GRIN1):c.2265C>T (p.Arg755=) rs748101281
NM_007327.4(GRIN1):c.2298C>T (p.Ser766=) rs138298331
NM_007327.4(GRIN1):c.2313C>T (p.Asn771=) rs201881481
NM_007327.4(GRIN1):c.2320C>T (p.Leu774=)
NM_007327.4(GRIN1):c.2333+6T>C
NM_007327.4(GRIN1):c.2352C>T (p.Phe784=)
NM_007327.4(GRIN1):c.2412C>G (p.Ala804=) rs149053552
NM_007327.4(GRIN1):c.2414del (p.Pro805fs)
NM_007327.4(GRIN1):c.2424T>C (p.Leu808=)
NM_007327.4(GRIN1):c.2443+7T>G
NM_007327.4(GRIN1):c.2444-10C>T rs200762696
NM_007327.4(GRIN1):c.2445G>A (p.Gly815=) rs367543117
NM_007327.4(GRIN1):c.2488C>T (p.Leu830=) rs746335646
NM_007327.4(GRIN1):c.2499C>T (p.Ile833=) rs146086141
NM_007327.4(GRIN1):c.2515C>A (p.Arg839=)
NM_007327.4(GRIN1):c.2532C>T (p.Arg844=)
NM_007327.4(GRIN1):c.2535G>A (p.Arg845=)
NM_007327.4(GRIN1):c.255C>T (p.Ser85=) rs797045605
NM_007327.4(GRIN1):c.2583C>T (p.Asn861=)
NM_007327.4(GRIN1):c.259-10G>A rs1161777906
NM_007327.4(GRIN1):c.259-9T>C rs1554766108
NM_007327.4(GRIN1):c.2595A>G (p.Arg865=) rs770728444
NM_007327.4(GRIN1):c.2598G>A (p.Lys866=)
NM_007327.4(GRIN1):c.2690C>T (p.Ser897Phe)
NM_007327.4(GRIN1):c.2718C>T (p.Arg906=)
NM_007327.4(GRIN1):c.2799C>T (p.Ser933=) rs201012245
NM_007327.4(GRIN1):c.286C>T (p.Pro96Ser)
NM_007327.4(GRIN1):c.303C>T (p.His101=)
NM_007327.4(GRIN1):c.351C>G (p.Pro117=) rs772616726
NM_007327.4(GRIN1):c.351C>T (p.Pro117=) rs772616726
NM_007327.4(GRIN1):c.360G>A (p.Gly120=)
NM_007327.4(GRIN1):c.36G>C (p.Leu12=) rs747107321
NM_007327.4(GRIN1):c.378C>T (p.Ser126=) rs1588686368
NM_007327.4(GRIN1):c.381C>T (p.Ile127=)
NM_007327.4(GRIN1):c.387G>C (p.Ser129=) rs199799811
NM_007327.4(GRIN1):c.394-4G>A rs202180269
NM_007327.4(GRIN1):c.403C>T (p.Leu135=) rs200400213
NM_007327.4(GRIN1):c.420C>T (p.Thr140=) rs771424493
NM_007327.4(GRIN1):c.426G>A (p.Pro142=) rs201424528
NM_007327.4(GRIN1):c.451T>C (p.Trp151Arg)
NM_007327.4(GRIN1):c.513C>T (p.His171=)
NM_007327.4(GRIN1):c.528T>A (p.Ala176=) rs1588694991
NM_007327.4(GRIN1):c.546G>A (p.Thr182=) rs77854056
NM_007327.4(GRIN1):c.570+4A>T rs200019763
NM_007327.4(GRIN1):c.571-5C>T
NM_007327.4(GRIN1):c.609C>T (p.Asn203=)
NM_007327.4(GRIN1):c.621G>C (p.Leu207=)
NM_007327.4(GRIN1):c.630G>A (p.Glu210=) rs1057522916
NM_007327.4(GRIN1):c.633G>A (p.Ala211=) rs150405897
NM_007327.4(GRIN1):c.63G>A (p.Ala21=) rs759756646
NM_007327.4(GRIN1):c.654C>T (p.Val218=)
NM_007327.4(GRIN1):c.669C>G (p.Ala223=) rs766714775
NM_007327.4(GRIN1):c.66C>T (p.Cys22=) rs148688400
NM_007327.4(GRIN1):c.696C>T (p.Tyr232=) rs200390848
NM_007327.4(GRIN1):c.705C>A (p.Ala235=)
NM_007327.4(GRIN1):c.705C>T (p.Ala235=) rs201343933
NM_007327.4(GRIN1):c.738G>A (p.Val246=)
NM_007327.4(GRIN1):c.780C>T (p.Arg260=) rs3181450
NM_007327.4(GRIN1):c.78C>T (p.Ile26=)
NM_007327.4(GRIN1):c.802G>A (p.Gly268Arg)
NM_007327.4(GRIN1):c.819C>T (p.Asn273=) rs1255557713
NM_007327.4(GRIN1):c.888C>T (p.Leu296=) rs770334644
NM_007327.4(GRIN1):c.912G>A (p.Pro304=) rs202240473
NM_007327.4(GRIN1):c.968+10G>A
NM_007327.4(GRIN1):c.968+10dup rs777548072
NM_007327.4(GRIN1):c.968+7G>A
NM_007327.4(GRIN1):c.969-5C>T
NM_007327.4(GRIN1):c.996T>C (p.Asp332=)
NM_007327.4(GRIN1):c.9C>T (p.Thr3=)

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