ClinVar Miner

List of variants in gene GRIN1 reported as uncertain significance by GeneDx

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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_007327.4(GRIN1):c.1382A>G (p.Asp461Gly) rs955781126 0.00003
NM_007327.4(GRIN1):c.505G>A (p.Asp169Asn) rs886039622 0.00002
NM_007327.4(GRIN1):c.1485G>C (p.Lys495Asn) rs779906300 0.00001
NM_007327.4(GRIN1):c.2014-5T>G rs1159926920 0.00001
NM_007327.4(GRIN1):c.2690C>T (p.Ser897Phe) rs764554048 0.00001
NM_007327.4(GRIN1):c.700G>A (p.Ala234Thr) rs1464941427 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.1004C>G (p.Thr335Ser)
NM_007327.4(GRIN1):c.103A>G (p.Thr35Ala) rs2131186563
NM_007327.4(GRIN1):c.1237C>T (p.Pro413Ser)
NM_007327.4(GRIN1):c.1255A>C (p.Thr419Pro)
NM_007327.4(GRIN1):c.1271T>C (p.Phe424Ser) rs1236518931
NM_007327.4(GRIN1):c.1359G>C (p.Gln453His) rs1374644440
NM_007327.4(GRIN1):c.1483A>C (p.Lys495Gln)
NM_007327.4(GRIN1):c.1555A>G (p.Ile519Val)
NM_007327.4(GRIN1):c.1567C>T (p.Arg523Cys) rs2131296364
NM_007327.4(GRIN1):c.1570G>C (p.Ala524Pro)
NM_007327.4(GRIN1):c.1579A>C (p.Ile527Leu) rs2131296416
NM_007327.4(GRIN1):c.160G>A (p.Gly54Ser)
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)
NM_007327.4(GRIN1):c.183T>A (p.Asn61Lys) rs779776822
NM_007327.4(GRIN1):c.1888C>T (p.Arg630Cys)
NM_007327.4(GRIN1):c.1902G>A (p.Met634Ile) rs2131299071
NM_007327.4(GRIN1):c.1946C>T (p.Ala649Val)
NM_007327.4(GRIN1):c.2080C>T (p.Arg694Trp) rs146204733
NM_007327.4(GRIN1):c.2129A>G (p.Asn710Ser)
NM_007327.4(GRIN1):c.2172C>T (p.Asn724=) rs2131301112
NM_007327.4(GRIN1):c.2204T>G (p.Val735Gly)
NM_007327.4(GRIN1):c.2302T>G (p.Trp768Gly)
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.237C>A (p.Cys79Ter) rs200529044
NM_007327.4(GRIN1):c.2386C>G (p.Gln796Glu) rs2131302611
NM_007327.4(GRIN1):c.2442C>G (p.Ala814=) rs773708731
NM_007327.4(GRIN1):c.2468G>A (p.Gly823Asp) rs2131303171
NM_007327.4(GRIN1):c.2560G>T (p.Ala854Ser) rs2131303448
NM_007327.4(GRIN1):c.2690C>G (p.Ser897Cys) rs764554048
NM_007327.4(GRIN1):c.2693_2694del (p.Lys898fs)
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.2815T>C (p.Ter939Arg) rs2131315142
NM_007327.4(GRIN1):c.362T>C (p.Leu121Pro)
NM_007327.4(GRIN1):c.368C>A (p.Thr123Asn)
NM_007327.4(GRIN1):c.415C>T (p.Arg139Cys)
NM_007327.4(GRIN1):c.5G>A (p.Ser2Asn)
NM_007327.4(GRIN1):c.679G>A (p.Asp227Asn)
NM_007327.4(GRIN1):c.691G>C (p.Val231Leu)
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.784G>A (p.Ala262Thr)
NM_007327.4(GRIN1):c.794-9C>T rs2131272367
NM_007327.4(GRIN1):c.794G>A (p.Gly265Asp) rs2131272421
NM_007327.4(GRIN1):c.845G>A (p.Ser282Asn)
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.947A>G (p.Lys316Arg) rs1554768797
NM_007327.4(GRIN1):c.962T>G (p.Phe321Cys)

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