ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 135
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HGVS dbSNP gnomAD frequency
NM_007327.4(GRIN1):c.2444-14G>A rs191352124 0.00024
NM_007327.4(GRIN1):c.1012G>A (p.Val338Met) rs140672142 0.00015
NM_007327.4(GRIN1):c.705C>T (p.Ala235=) rs201343933 0.00011
NM_007327.4(GRIN1):c.610G>A (p.Val204Met) rs140422926 0.00009
NM_007327.4(GRIN1):c.1339C>T (p.Pro447Ser) rs763222643 0.00007
NM_007327.4(GRIN1):c.1076G>A (p.Arg359His) rs141704101 0.00004
NM_007327.4(GRIN1):c.1045G>T (p.Ala349Ser) rs148008303 0.00003
NM_007327.4(GRIN1):c.1382A>G (p.Asp461Gly) rs955781126 0.00003
NM_007327.4(GRIN1):c.2589+6G>T rs200395927 0.00003
NM_007327.4(GRIN1):c.505G>A (p.Asp169Asn) rs886039622 0.00002
NM_007327.4(GRIN1):c.1108A>G (p.Thr370Ala) rs746527135 0.00001
NM_007327.4(GRIN1):c.1247G>A (p.Ser416Asn) rs1833513036 0.00001
NM_007327.4(GRIN1):c.1485G>C (p.Lys495Asn) rs779906300 0.00001
NM_007327.4(GRIN1):c.160G>A (p.Gly54Ser) rs2538508186 0.00001
NM_007327.4(GRIN1):c.2014-5T>G rs1159926920 0.00001
NM_007327.4(GRIN1):c.237C>T (p.Cys79=) rs200529044 0.00001
NM_007327.4(GRIN1):c.2442C>T (p.Ala814=) rs773708731 0.00001
NM_007327.4(GRIN1):c.2681G>A (p.Arg894His) rs1833804499 0.00001
NM_007327.4(GRIN1):c.2690C>T (p.Ser897Phe) rs764554048 0.00001
NM_007327.4(GRIN1):c.368C>A (p.Thr123Asn) rs1564340685 0.00001
NM_007327.4(GRIN1):c.521G>A (p.Arg174Gln) rs758521939 0.00001
NM_007327.4(GRIN1):c.570+18G>A rs200220418 0.00001
NM_007327.4(GRIN1):c.691G>C (p.Val231Leu) rs1472478100 0.00001
NM_007327.4(GRIN1):c.700G>A (p.Ala234Thr) rs1464941427 0.00001
NM_007327.4(GRIN1):c.845G>A (p.Ser282Asn) rs1320100124 0.00001
NM_007327.4(GRIN1):c.907G>A (p.Asp303Asn) rs200758208 0.00001
NM_007327.4(GRIN1):c.996T>A (p.Asp332Glu) rs1833354106 0.00001
NM_007327.4(GRIN1):c.*301A>G
NM_007327.4(GRIN1):c.1004C>G (p.Thr335Ser) rs2538608046
NM_007327.4(GRIN1):c.1007G>T (p.Gly336Val) rs2538608073
NM_007327.4(GRIN1):c.1016A>G (p.Glu339Gly) rs1833355374
NM_007327.4(GRIN1):c.103A>G (p.Thr35Ala) rs2131186563
NM_007327.4(GRIN1):c.1114G>C (p.Val372Leu)
NM_007327.4(GRIN1):c.1125T>A (p.Asn375Lys)
NM_007327.4(GRIN1):c.1126G>T (p.Asp376Tyr) rs2538610058
NM_007327.4(GRIN1):c.1236G>T (p.Lys412Asn)
NM_007327.4(GRIN1):c.1237C>T (p.Pro413Ser) rs2538623973
NM_007327.4(GRIN1):c.1255A>C (p.Thr419Pro) rs763133592
NM_007327.4(GRIN1):c.1271T>C (p.Phe424Ser) rs1236518931
NM_007327.4(GRIN1):c.1312G>A (p.Gly438Arg)
NM_007327.4(GRIN1):c.1334G>A (p.Gly445Asp) rs147435860
NM_007327.4(GRIN1):c.1340C>T (p.Pro447Leu) rs587780348
NM_007327.4(GRIN1):c.1359G>C (p.Gln453His) rs1374644440
NM_007327.4(GRIN1):c.1366T>C (p.Tyr456His) rs2538626520
NM_007327.4(GRIN1):c.1445G>T (p.Gly482Val) rs2131292828
NM_007327.4(GRIN1):c.1448A>G (p.Lys483Arg)
NM_007327.4(GRIN1):c.1452C>A (p.Phe484Leu) rs1833532800
NM_007327.4(GRIN1):c.1468G>A (p.Val490Met)
NM_007327.4(GRIN1):c.1483A>C (p.Lys495Gln) rs1833574504
NM_007327.4(GRIN1):c.1555A>G (p.Ile519Val) rs2538634543
NM_007327.4(GRIN1):c.1567C>T (p.Arg523Cys) rs2131296364
NM_007327.4(GRIN1):c.1569C>A (p.Arg523=) rs1833579629
NM_007327.4(GRIN1):c.1570G>C (p.Ala524Pro) rs954781478
NM_007327.4(GRIN1):c.1579A>C (p.Ile527Leu) rs2131296416
NM_007327.4(GRIN1):c.1583A>G (p.Glu528Gly)
NM_007327.4(GRIN1):c.1616C>A (p.Thr539Asn) rs2131296564
NM_007327.4(GRIN1):c.1616C>T (p.Thr539Ile) rs2131296564
NM_007327.4(GRIN1):c.1687T>G (p.Trp563Gly) rs2538637096
NM_007327.4(GRIN1):c.1752C>A (p.Ser584Arg)
NM_007327.4(GRIN1):c.1762C>T (p.Arg588Trp)
NM_007327.4(GRIN1):c.1765T>C (p.Phe589Leu) rs1564363549
NM_007327.4(GRIN1):c.1786G>A (p.Glu596Lys)
NM_007327.4(GRIN1):c.1795G>C (p.Asp599His)
NM_007327.4(GRIN1):c.183T>A (p.Asn61Lys) rs779776822
NM_007327.4(GRIN1):c.1848C>G (p.Asn616Lys) rs2538639584
NM_007327.4(GRIN1):c.1864+6G>T rs2538639727
NM_007327.4(GRIN1):c.1888C>T (p.Arg630Cys) rs2538640396
NM_007327.4(GRIN1):c.1902G>A (p.Met634Ile) rs2131299071
NM_007327.4(GRIN1):c.1946C>T (p.Ala649Val) rs2538640891
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.2039_2042del (p.Ile680fs) rs1564364189
NM_007327.4(GRIN1):c.2051T>C (p.Val684Ala) rs2538642803
NM_007327.4(GRIN1):c.2054A>G (p.Lys685Arg) rs1292632620
NM_007327.4(GRIN1):c.2070T>G (p.Asp690Glu)
NM_007327.4(GRIN1):c.2072T>G (p.Ile691Ser)
NM_007327.4(GRIN1):c.2080C>T (p.Arg694Trp) rs146204733
NM_007327.4(GRIN1):c.2081G>A (p.Arg694Gln)
NM_007327.4(GRIN1):c.209A>G (p.Asn70Ser)
NM_007327.4(GRIN1):c.2105T>C (p.Met702Thr) rs2131300169
NM_007327.4(GRIN1):c.2122A>C (p.Lys708Gln) rs1564364339
NM_007327.4(GRIN1):c.2129A>G (p.Asn710Ser) rs2538643174
NM_007327.4(GRIN1):c.2138G>A (p.Ser713Asn) rs2538643232
NM_007327.4(GRIN1):c.2141C>A (p.Ala714Glu)
NM_007327.4(GRIN1):c.2172C>T (p.Asn724=) rs2131301112
NM_007327.4(GRIN1):c.2199G>A (p.Ser733=) rs1554770437
NM_007327.4(GRIN1):c.2204T>G (p.Val735Gly) rs2538645065
NM_007327.4(GRIN1):c.2215G>C (p.Glu739Gln) rs2538645128
NM_007327.4(GRIN1):c.2302T>G (p.Trp768Gly) rs2538645685
NM_007327.4(GRIN1):c.230C>T (p.Ser77Leu) rs2131187092
NM_007327.4(GRIN1):c.2327T>C (p.Ile776Thr) rs2131301519
NM_007327.4(GRIN1):c.2341G>A (p.Glu781Lys)
NM_007327.4(GRIN1):c.237C>A (p.Cys79Ter) rs200529044
NM_007327.4(GRIN1):c.2386C>G (p.Gln796Glu) rs2131302611
NM_007327.4(GRIN1):c.2417C>T (p.Ala806Val) rs1554770589
NM_007327.4(GRIN1):c.2442C>G (p.Ala814=) rs773708731
NM_007327.4(GRIN1):c.2444-16G>A rs896361924
NM_007327.4(GRIN1):c.2468G>A (p.Gly823Asp) rs2131303171
NM_007327.4(GRIN1):c.2473G>C (p.Val825Leu)
NM_007327.4(GRIN1):c.2560G>T (p.Ala854Ser) rs2131303448
NM_007327.4(GRIN1):c.2576G>A (p.Arg859Gln) rs2131303507
NM_007327.4(GRIN1):c.2589+5G>A rs2131303553
NM_007327.4(GRIN1):c.2690C>G (p.Ser897Cys) rs764554048
NM_007327.4(GRIN1):c.2693_2694del (p.Lys898fs) rs2538658423
NM_007327.4(GRIN1):c.2705C>G (p.Thr902Ser) rs2131314853
NM_007327.4(GRIN1):c.2723C>G (p.Ala908Gly) rs2131314946
NM_007327.4(GRIN1):c.2756G>C (p.Arg919Pro)
NM_007327.4(GRIN1):c.2815T>C (p.Ter939Arg) rs2131315142
NM_007327.4(GRIN1):c.284C>A (p.Pro95Gln)
NM_007327.4(GRIN1):c.362T>C (p.Leu121Pro) rs2538516794
NM_007327.4(GRIN1):c.415C>T (p.Arg139Cys) rs1832493628
NM_007327.4(GRIN1):c.416G>A (p.Arg139His) rs747555101
NM_007327.4(GRIN1):c.430T>G (p.Tyr144Asp) rs2131217127
NM_007327.4(GRIN1):c.44G>C (p.Cys15Ser)
NM_007327.4(GRIN1):c.508G>C (p.Asp170His)
NM_007327.4(GRIN1):c.536G>A (p.Arg179His)
NM_007327.4(GRIN1):c.5G>A (p.Ser2Asn) rs1832047745
NM_007327.4(GRIN1):c.679G>A (p.Asp227Asn) rs869312865
NM_007327.4(GRIN1):c.722C>T (p.Thr241Met) rs1228808440
NM_007327.4(GRIN1):c.734A>T (p.Tyr245Phe) rs893141433
NM_007327.4(GRIN1):c.759G>A (p.Glu253=) rs1064797354
NM_007327.4(GRIN1):c.784G>A (p.Ala262Thr) rs2538595748
NM_007327.4(GRIN1):c.794-9C>T rs2131272367
NM_007327.4(GRIN1):c.794G>A (p.Gly265Asp) rs2131272421
NM_007327.4(GRIN1):c.83A>T (p.Asn28Ile)
NM_007327.4(GRIN1):c.879C>G (p.His293Gln) rs746040843
NM_007327.4(GRIN1):c.879_880insCTCGAT (p.His293_Glu294insLeuAsp) rs1554768765
NM_007327.4(GRIN1):c.892_894del (p.Lys298del) rs1455640330
NM_007327.4(GRIN1):c.943T>G (p.Trp315Gly)
NM_007327.4(GRIN1):c.947A>G (p.Lys316Arg) rs1554768797
NM_007327.4(GRIN1):c.955C>A (p.Pro319Thr) rs1833266868
NM_007327.4(GRIN1):c.955C>T (p.Pro319Ser) rs1833266868
NM_007327.4(GRIN1):c.962T>G (p.Phe321Cys) rs2538598027
NM_007327.4(GRIN1):c.980C>A (p.Ser327Tyr)
Single allele

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