ClinVar Miner

List of variants in gene GRIN1 reported as benign

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Gene type:
ClinVar version:
Total variants: 57
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HGVS dbSNP
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.1098C>G (p.Ile366Met) rs778196924
NM_007327.4(GRIN1):c.1108A>G (p.Thr370Ala) rs746527135
NM_007327.4(GRIN1):c.1131G>A (p.Arg377=)
NM_007327.4(GRIN1):c.1149C>T (p.Gly383=) rs138398771
NM_007327.4(GRIN1):c.1168C>G (p.Arg390Gly)
NM_007327.4(GRIN1):c.1198-3del rs762423431
NM_007327.4(GRIN1):c.1198-7C>T rs202163066
NM_007327.4(GRIN1):c.1335C>T (p.Gly445=)
NM_007327.4(GRIN1):c.1340-38G>A rs41290007
NM_007327.4(GRIN1):c.1340C>A (p.Pro447His) rs587780348
NM_007327.4(GRIN1):c.1467+160G>A rs11146026
NM_007327.4(GRIN1):c.1467+182C>T rs143767330
NM_007327.4(GRIN1):c.1467+202T>C rs10870200
NM_007327.4(GRIN1):c.1467+8G>A rs10747050
NM_007327.4(GRIN1):c.1468-219_1468-204del rs36070681
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.154C>G (p.Arg52Gly) rs950054021
NM_007327.4(GRIN1):c.1584G>A (p.Glu528=) rs116006955
NM_007327.4(GRIN1):c.1632+17_1632+23del
NM_007327.4(GRIN1):c.1716G>A (p.Val572=)
NM_007327.4(GRIN1):c.1809G>C (p.Leu603=) rs141249927
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.22A>C (p.Thr8Pro)
NM_007327.4(GRIN1):c.2328C>T (p.Ile776=) rs200088954
NM_007327.4(GRIN1):c.2333+9C>A rs201316377
NM_007327.4(GRIN1):c.2334G>A (p.Lys778=)
NM_007327.4(GRIN1):c.237C>T (p.Cys79=) rs200529044
NM_007327.4(GRIN1):c.246C>T (p.Leu82=) rs192006771
NM_007327.4(GRIN1):c.258+235C>T rs2301363
NM_007327.4(GRIN1):c.2614C>G (p.Pro872Ala)
NM_007327.4(GRIN1):c.394-11G>A rs75081117
NM_007327.4(GRIN1):c.394-139C>A rs11146023
NM_007327.4(GRIN1):c.394-176_394-175insA rs71387806
NM_007327.4(GRIN1):c.394-188_394-130del rs1564344660
NM_007327.4(GRIN1):c.507C>T (p.Asp169=) rs199720207
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+263G>C rs9411312
NM_007327.4(GRIN1):c.571-1141G>A rs10870198
NM_007327.4(GRIN1):c.614C>T (p.Thr205Met) rs201592328
NM_007327.4(GRIN1):c.672-106A>C rs28507734
NM_007327.4(GRIN1):c.672-134A>G rs28514863
NM_007327.4(GRIN1):c.672-267_672-229del rs755849037
NM_007327.4(GRIN1):c.672-330A>G rs115011370
NM_007327.4(GRIN1):c.672-80A>G rs28687864
NM_007327.4(GRIN1):c.693A>C (p.Val231=) rs201818201
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.855G>A (p.Val285=) rs1126442
NM_007327.4(GRIN1):c.968+274A>G rs73571550
NM_007327.4(GRIN1):c.969-177G>A rs28408401
NM_007327.4(GRIN1):c.992C>T (p.Ala331Val)

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