ClinVar Miner

List of variants in gene GRIN1 reported as uncertain significance for not provided

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Gene type:
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Total variants: 23
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HGVS dbSNP
NM_007327.4(GRIN1):c.1012G>A (p.Val338Met) rs140672142
NM_007327.4(GRIN1):c.1045G>T (p.Ala349Ser) rs148008303
NM_007327.4(GRIN1):c.1108A>G (p.Thr370Ala) rs746527135
NM_007327.4(GRIN1):c.1331C>T (p.Pro444Leu) rs200225692
NM_007327.4(GRIN1):c.1339C>T (p.Pro447Ser)
NM_007327.4(GRIN1):c.1340C>T (p.Pro447Leu) rs587780348
NM_007327.4(GRIN1):c.1765T>C (p.Phe589Leu) rs1564363549
NM_007327.4(GRIN1):c.1974C>G (p.Asp658Glu) rs1064795712
NM_007327.4(GRIN1):c.2008C>T (p.Pro670Ser) rs1057520055
NM_007327.4(GRIN1):c.2122A>C (p.Lys708Gln) rs1564364339
NM_007327.4(GRIN1):c.2199G>A (p.Ser733=) rs1554770437
NM_007327.4(GRIN1):c.2223G>C (p.Ser741=) rs767848286
NM_007327.4(GRIN1):c.237C>A (p.Cys79Ter) rs200529044
NM_007327.4(GRIN1):c.2417C>T (p.Ala806Val) rs1554770589
NM_007327.4(GRIN1):c.2442C>T (p.Ala814=) rs773708731
NM_007327.4(GRIN1):c.2589+6G>T rs200395927
NM_007327.4(GRIN1):c.505G>A (p.Asp169Asn) rs886039622
NM_007327.4(GRIN1):c.705C>T (p.Ala235=) rs201343933
NM_007327.4(GRIN1):c.759G>A (p.Glu253=) rs1064797354
NM_007327.4(GRIN1):c.780C>T (p.Arg260=) rs3181450
NM_007327.4(GRIN1):c.879_880insCTCGAT (p.Glu294_Leu295insLeuAsp) rs1554768765
NM_007327.4(GRIN1):c.947A>G (p.Lys316Arg) rs1554768797
Single allele

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