ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 26
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HGVS dbSNP
NM_007327.4(GRIN1):c.1005T>C (p.Thr335=) rs145176345
NM_007327.4(GRIN1):c.1098C>G (p.Ile366Met) rs778196924
NM_007327.4(GRIN1):c.1340-38G>A rs41290007
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.1548G>A (p.Pro516=) rs75783429
NM_007327.4(GRIN1):c.1584G>A (p.Glu528=) rs116006955
NM_007327.4(GRIN1):c.2328C>T (p.Ile776=) rs200088954
NM_007327.4(GRIN1):c.258+235C>T rs2301363
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.570+263G>C rs9411312
NM_007327.4(GRIN1):c.571-1141G>A rs10870198
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.768G>C (p.Gly256=) rs141473515
NM_007327.4(GRIN1):c.789A>G (p.Pro263=) rs6293
NM_007327.4(GRIN1):c.968+274A>G rs73571550
NM_007327.4(GRIN1):c.969-177G>A rs28408401

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