ClinVar Miner

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

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Gene type:
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Total variants: 40
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HGVS dbSNP
NM_007327.4(GRIN1):c.1197+7G>A rs1588721709
NM_007327.4(GRIN1):c.1206G>A (p.Thr402=) rs548201762
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.1344C>T (p.Arg448=) rs200574152
NM_007327.4(GRIN1):c.1431C>T (p.His477=) rs1057522926
NM_007327.4(GRIN1):c.1449G>A (p.Lys483=) rs778957098
NM_007327.4(GRIN1):c.1468-10C>T rs1226232806
NM_007327.4(GRIN1):c.1513C>T (p.Leu505=) rs139637382
NM_007327.4(GRIN1):c.152A>G (p.Lys51Arg) rs767000671
NM_007327.4(GRIN1):c.159C>T (p.His53=) rs147818786
NM_007327.4(GRIN1):c.1650G>A (p.Thr550=) rs1588731007
NM_007327.4(GRIN1):c.1671G>C (p.Pro557=) rs1348812038
NM_007327.4(GRIN1):c.1776C>T (p.Asn592=) rs369596145
NM_007327.4(GRIN1):c.1806C>T (p.Thr602=) rs1039715252
NM_007327.4(GRIN1):c.2097G>C (p.Leu699=) rs143865216
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.231G>A (p.Ser77=) rs1219867246
NM_007327.4(GRIN1):c.2328C>T (p.Ile776=) rs200088954
NM_007327.4(GRIN1):c.2444-10C>T rs200762696
NM_007327.4(GRIN1):c.2472C>A (p.Ile824=)
NM_007327.4(GRIN1):c.258+18C>T rs202160831
NM_007327.4(GRIN1):c.258+19G>A rs1447155507
NM_007327.4(GRIN1):c.259-203G>A rs78889075
NM_007327.4(GRIN1):c.2799C>T (p.Ser933=) rs201012245
NM_007327.4(GRIN1):c.357G>A (p.Leu119=) rs201475721
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.394-22_394-20delinsACT rs1588694679
NM_007327.4(GRIN1):c.394-32A>G rs200424067
NM_007327.4(GRIN1):c.420C>T (p.Thr140=) rs771424493
NM_007327.4(GRIN1):c.528T>A (p.Ala176=) rs1588694991
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.672-147C>T rs117627988
NM_007327.4(GRIN1):c.672-148G>A rs117281178
NM_007327.4(GRIN1):c.819C>T (p.Asn273=) rs1255557713
NM_007327.4(GRIN1):c.912G>A (p.Pro304=) rs202240473
NM_007327.4(GRIN1):c.968+10dup rs777548072

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