ClinVar Miner

List of variants in gene GRIN1 reported as uncertain significance for Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant

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Total variants: 82
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HGVS dbSNP
NC_000009.12:g.(?_137139467)_(137139764_?)dup
NC_000009.12:g.(?_137139467)_(137167862_?)dup
NM_007327.4(GRIN1):c.1037G>A (p.Arg346Gln)
NM_007327.4(GRIN1):c.1076G>A (p.Arg359His) rs141704101
NM_007327.4(GRIN1):c.1113C>T (p.His371=) rs150508714
NM_007327.4(GRIN1):c.1114-3C>T
NM_007327.4(GRIN1):c.1169G>A (p.Arg390Gln)
NM_007327.4(GRIN1):c.1198-2del rs1212517874
NM_007327.4(GRIN1):c.1198-3C>T rs200368768
NM_007327.4(GRIN1):c.1248T>A (p.Ser416Arg)
NM_007327.4(GRIN1):c.1255A>G (p.Thr419Ala)
NM_007327.4(GRIN1):c.1339+15C>T
NM_007327.4(GRIN1):c.1339C>T (p.Pro447Ser)
NM_007327.4(GRIN1):c.1343G>A (p.Arg448His)
NM_007327.4(GRIN1):c.1359G>C (p.Gln453His)
NM_007327.4(GRIN1):c.1376G>A (p.Cys459Tyr)
NM_007327.4(GRIN1):c.1382A>G (p.Asp461Gly) rs955781126
NM_007327.4(GRIN1):c.1403G>A (p.Arg468Gln)
NM_007327.4(GRIN1):c.1452C>A (p.Phe484Leu)
NM_007327.4(GRIN1):c.1468-8C>A
NM_007327.4(GRIN1):c.1483A>G (p.Lys495Glu)
NM_007327.4(GRIN1):c.1516C>T (p.Leu506Phe) rs778079350
NM_007327.4(GRIN1):c.1538T>A (p.Ile513Asn)
NM_007327.4(GRIN1):c.1647C>T (p.Ser549=) rs1052601804
NM_007327.4(GRIN1):c.1761C>T (p.Gly587=)
NM_007327.4(GRIN1):c.1913G>C (p.Gly638Ala)
NM_007327.4(GRIN1):c.1927A>G (p.Ile643Val) rs1554770243
NM_007327.4(GRIN1):c.1961T>C (p.Phe654Ser)
NM_007327.4(GRIN1):c.1964T>A (p.Leu655Gln) rs1564363923
NM_007327.4(GRIN1):c.1971G>A (p.Leu657=) rs1564363935
NM_007327.4(GRIN1):c.1979C>T (p.Pro660Leu) rs1328780843
NM_007327.4(GRIN1):c.1A>T (p.Met1Leu) rs780712950
NM_007327.4(GRIN1):c.2172-3C>T
NM_007327.4(GRIN1):c.2172-5G>A rs1588734042
NM_007327.4(GRIN1):c.2188A>C (p.Ile730Leu)
NM_007327.4(GRIN1):c.2314G>C (p.Val772Leu) rs1060500045
NM_007327.4(GRIN1):c.2333+3G>A rs962894112
NM_007327.4(GRIN1):c.2334-10C>A
NM_007327.4(GRIN1):c.238G>A (p.Glu80Lys) rs748041860
NM_007327.4(GRIN1):c.2414C>T (p.Pro805Leu) rs1588735247
NM_007327.4(GRIN1):c.2442C>T (p.Ala814=) rs773708731
NM_007327.4(GRIN1):c.2444G>A (p.Gly815Glu)
NM_007327.4(GRIN1):c.2479G>A (p.Gly827Arg) rs1451230055
NM_007327.4(GRIN1):c.2500G>C (p.Glu834Gln) rs1588735834
NM_007327.4(GRIN1):c.2516G>A (p.Arg839Gln)
NM_007327.4(GRIN1):c.2531G>T (p.Arg844Leu) rs1564365418
NM_007327.4(GRIN1):c.2534G>A (p.Arg845Gln) rs1405592274
NM_007327.4(GRIN1):c.2589+6G>T rs200395927
NM_007327.4(GRIN1):c.2654C>T (p.Ser885Phe)
NM_007327.4(GRIN1):c.2689T>A (p.Ser897Thr)
NM_007327.4(GRIN1):c.2700+6G>A
NM_007327.4(GRIN1):c.2700+8G>T rs201887636
NM_007327.4(GRIN1):c.2700G>A (p.Thr900=) rs1588739764
NM_007327.4(GRIN1):c.2716C>A (p.Arg906Ser) rs200007767
NM_007327.4(GRIN1):c.2720G>C (p.Gly907Ala)
NM_007327.4(GRIN1):c.2805T>A (p.His935Gln)
NM_007327.4(GRIN1):c.334G>A (p.Gly112Ser)
NM_007327.4(GRIN1):c.344G>A (p.Arg115His)
NM_007327.4(GRIN1):c.35T>C (p.Leu12Pro)
NM_007327.4(GRIN1):c.387G>A (p.Ser129=) rs199799811
NM_007327.4(GRIN1):c.41_43del (p.Ser14del)
NM_007327.4(GRIN1):c.421G>A (p.Val141Met)
NM_007327.4(GRIN1):c.448G>A (p.Val150Met)
NM_007327.4(GRIN1):c.466C>A (p.Arg156Ser)
NM_007327.4(GRIN1):c.467G>A (p.Arg156His) rs762490192
NM_007327.4(GRIN1):c.505G>A (p.Asp169Asn) rs886039622
NM_007327.4(GRIN1):c.510C>A (p.Asp170Glu) rs765185253
NM_007327.4(GRIN1):c.524C>T (p.Ala175Val) rs200577112
NM_007327.4(GRIN1):c.570G>A (p.Lys190=)
NM_007327.4(GRIN1):c.610G>A (p.Val204Met)
NM_007327.4(GRIN1):c.631G>A (p.Ala211Thr) rs768760751
NM_007327.4(GRIN1):c.711G>A (p.Met237Ile)
NM_007327.4(GRIN1):c.734A>T (p.Tyr245Phe) rs893141433
NM_007327.4(GRIN1):c.747C>A (p.Val249=)
NM_007327.4(GRIN1):c.794-11T>A
NM_007327.4(GRIN1):c.799C>A (p.Leu267Ile)
NM_007327.4(GRIN1):c.907G>T (p.Asp303Tyr) rs200758208
NM_007327.4(GRIN1):c.955C>A (p.Pro319Thr)
NM_007327.4(GRIN1):c.957G>A (p.Pro319=) rs766888803
NM_007327.4(GRIN1):c.989A>G (p.Tyr330Cys)
NM_007327.4(GRIN1):c.992C>A (p.Ala331Glu)
NM_007327.4(GRIN1):c.993G>A (p.Ala331=)

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