List of variants in gene L1CAM reported as uncertain significance for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 121

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HGVS	dbSNP	gnomAD frequency
NC_000023.11:g.153859456A>G	rs868935535	0.00267
NM_001278116.2(L1CAM):c.2302G>A (p.Val768Ile)	rs36021462	0.00178
NM_001278116.2(L1CAM):c.630C>T (p.His210=)	rs28933683	0.00031
NM_001278116.2(L1CAM):c.3192G>T (p.Ser1064=)	rs142563956	0.00028
NM_001278116.2(L1CAM):c.963C>T (p.Ala321=)	rs145823218	0.00021
NM_001278116.2(L1CAM):c.256G>A (p.Val86Met)	rs149309725	0.00017
NM_001278116.2(L1CAM):c.3057T>G (p.Asp1019Glu)	rs200815347	0.00012
NM_001278116.2(L1CAM):c.1993C>G (p.Leu665Val)	rs199592861	0.00010
NM_001278116.2(L1CAM):c.3434G>A (p.Arg1145His)	rs952497509	0.00007
NM_001278116.2(L1CAM):c.618C>A (p.Asp206Glu)	rs201474883	0.00007
NM_001278116.2(L1CAM):c.1107C>T (p.Asn369=)	rs200768501	0.00006
NM_001278116.2(L1CAM):c.2872+9G>A	rs398123363	0.00005
NM_001278116.2(L1CAM):c.367G>A (p.Ala123Thr)	rs782752037	0.00004
NM_001278116.2(L1CAM):c.386G>A (p.Arg129Gln)	rs200809259	0.00004
NM_001278116.2(L1CAM):c.2308G>A (p.Asp770Asn)	rs148516831	0.00003
NM_001278116.2(L1CAM):c.3523G>A (p.Glu1175Lys)	rs1064796541	0.00003
NM_001278116.2(L1CAM):c.385C>T (p.Arg129Trp)	rs201978087	0.00003
NM_001278116.2(L1CAM):c.1249G>A (p.Ala417Thr)	rs782331927	0.00002
NM_001278116.2(L1CAM):c.1379+3G>A	rs782455321	0.00002
NM_001278116.2(L1CAM):c.1387G>A (p.Glu463Lys)	rs202175564	0.00002
NM_001278116.2(L1CAM):c.1433C>A (p.Ala478Asp)	rs1298830102	0.00002
NM_001278116.2(L1CAM):c.1962C>T (p.Asp654=)	rs201372074	0.00002
NM_001278116.2(L1CAM):c.1978G>A (p.Glu660Lys)	rs200688598	0.00002
NM_001278116.2(L1CAM):c.202C>T (p.Arg68Cys)	rs1172761444	0.00002
NM_001278116.2(L1CAM):c.3326G>A (p.Arg1109His)	rs782420127	0.00002
NM_001278116.2(L1CAM):c.603C>T (p.Ser201=)	rs782223025	0.00002
NM_001278116.2(L1CAM):c.1180G>A (p.Val394Met)	rs782477425	0.00001
NM_001278116.2(L1CAM):c.1418G>A (p.Arg473His)	rs782516225	0.00001
NM_001278116.2(L1CAM):c.1841C>T (p.Pro614Leu)	rs1557091552	0.00001
NM_001278116.2(L1CAM):c.1880C>T (p.Thr627Met)	rs398123360	0.00001
NM_001278116.2(L1CAM):c.1894C>G (p.Arg632Gly)	rs782367123	0.00001
NM_001278116.2(L1CAM):c.2179G>A (p.Glu727Lys)	rs1386982536	0.00001
NM_001278116.2(L1CAM):c.219T>C (p.Gly73=)	rs1443862182	0.00001
NM_001278116.2(L1CAM):c.2722G>A (p.Glu908Lys)	rs199822230	0.00001
NM_001278116.2(L1CAM):c.2758C>T (p.His920Tyr)	rs2064701743	0.00001
NM_001278116.2(L1CAM):c.3118G>A (p.Glu1040Lys)	rs1557090130	0.00001
NM_001278116.2(L1CAM):c.3449A>G (p.Lys1150Arg)	rs1391080419	0.00001
NM_001278116.2(L1CAM):c.3654G>C (p.Gln1218His)	rs1369743518	0.00001
NM_001278116.2(L1CAM):c.591T>C (p.Asn197=)	rs375862497	0.00001
NM_001278116.2(L1CAM):c.666G>A (p.Lys222=)	rs782615469	0.00001
NM_001278116.2(L1CAM):c.726G>T (p.Leu242=)	rs200813995	0.00001
NM_001278116.2(L1CAM):c.860G>A (p.Arg287His)	rs200402620	0.00001
NM_001278116.2(L1CAM):c.1021A>C (p.Ser341Arg)	rs398123359
NM_001278116.2(L1CAM):c.1066G>T (p.Val356Phe)
NM_001278116.2(L1CAM):c.1118T>C (p.Val373Ala)
NM_001278116.2(L1CAM):c.1123+5G>A	rs1557092385
NM_001278116.2(L1CAM):c.1205C>G (p.Thr402Ser)	rs1222808372
NM_001278116.2(L1CAM):c.122C>G (p.Ser41Cys)
NM_001278116.2(L1CAM):c.1234C>G (p.Leu412Val)
NM_001278116.2(L1CAM):c.124C>T (p.Pro42Ser)
NM_001278116.2(L1CAM):c.1292C>A (p.Ala431Glu)	rs782779421
NM_001278116.2(L1CAM):c.1310T>C (p.Met437Thr)
NM_001278116.2(L1CAM):c.1316T>C (p.Val439Ala)	rs797044634
NM_001278116.2(L1CAM):c.1411G>A (p.Asp471Asn)	rs1603275442
NM_001278116.2(L1CAM):c.1414G>A (p.Glu472Lys)
NM_001278116.2(L1CAM):c.1445T>C (p.Leu482Pro)	rs1064794246
NM_001278116.2(L1CAM):c.1469_1474del (p.Asn490_Asp491del)	rs1085307881
NM_001278116.2(L1CAM):c.1475C>T (p.Thr492Ile)	rs2148496683
NM_001278116.2(L1CAM):c.1633C>T (p.Pro545Ser)	rs782513182
NM_001278116.2(L1CAM):c.1678C>T (p.Leu560Phe)	rs1414810082
NM_001278116.2(L1CAM):c.170G>A (p.Cys57Tyr)	rs1057517755
NM_001278116.2(L1CAM):c.1900T>C (p.Ser634Pro)	rs2148495976
NM_001278116.2(L1CAM):c.1972G>A (p.Ala658Thr)	rs2064725346
NM_001278116.2(L1CAM):c.2006C>G (p.Pro669Arg)
NM_001278116.2(L1CAM):c.2029C>T (p.Leu677Phe)
NM_001278116.2(L1CAM):c.2042C>T (p.Pro681Leu)	rs1557091354
NM_001278116.2(L1CAM):c.20A>G (p.Tyr7Cys)
NM_001278116.2(L1CAM):c.2137+5_2137+6insGGCAGGTGT	rs398123361
NM_001278116.2(L1CAM):c.2209C>G (p.Pro737Ala)
NM_001278116.2(L1CAM):c.2234C>T (p.Ala745Val)	rs2148495200
NM_001278116.2(L1CAM):c.2249A>C (p.Tyr750Ser)	rs1064794855
NM_001278116.2(L1CAM):c.2249A>G (p.Tyr750Cys)	rs1064794855
NM_001278116.2(L1CAM):c.2260T>A (p.Trp754Arg)	rs2148495173
NM_001278116.2(L1CAM):c.2279G>A (p.Arg760Gln)
NM_001278116.2(L1CAM):c.2311C>T (p.Pro771Ser)
NM_001278116.2(L1CAM):c.2343C>G (p.Phe781Leu)	rs369046420
NM_001278116.2(L1CAM):c.2368G>C (p.Ala790Pro)
NM_001278116.2(L1CAM):c.23T>A (p.Val8Glu)	rs886044768
NM_001278116.2(L1CAM):c.2416T>C (p.Tyr806His)	rs2064716073
NM_001278116.2(L1CAM):c.2516_2517delinsAT (p.Ala839Asp)	rs2148494375
NM_001278116.2(L1CAM):c.2539G>A (p.Gly847Arg)	rs2148494337
NM_001278116.2(L1CAM):c.2581_2589del (p.His861_Lys863del)
NM_001278116.2(L1CAM):c.2593C>T (p.His865Tyr)
NM_001278116.2(L1CAM):c.2607C>A (p.Asp869Glu)
NM_001278116.2(L1CAM):c.2648G>C (p.Ser883Thr)
NM_001278116.2(L1CAM):c.2739C>T (p.Thr913=)
NM_001278116.2(L1CAM):c.2748A>T (p.Gly916=)
NM_001278116.2(L1CAM):c.2849G>A (p.Gly950Asp)	rs886044872
NM_001278116.2(L1CAM):c.2852A>G (p.Tyr951Cys)
NM_001278116.2(L1CAM):c.2854G>A (p.Val952Met)
NM_001278116.2(L1CAM):c.2900C>T (p.Ser967Phe)
NM_001278116.2(L1CAM):c.2978T>C (p.Leu993Pro)	rs2148493621
NM_001278116.2(L1CAM):c.3014T>C (p.Ile1005Thr)	rs398123365
NM_001278116.2(L1CAM):c.3020G>A (p.Arg1007Gln)
NM_001278116.2(L1CAM):c.3046+5G>C
NM_001278116.2(L1CAM):c.3095G>A (p.Ser1032Asn)	rs2148493445
NM_001278116.2(L1CAM):c.3140T>C (p.Phe1047Ser)	rs2148493416
NM_001278116.2(L1CAM):c.3182C>A (p.Ala1061Asp)
NM_001278116.2(L1CAM):c.31CTC[2] (p.Leu13del)	rs2064809071
NM_001278116.2(L1CAM):c.3226A>T (p.Thr1076Ser)
NM_001278116.2(L1CAM):c.3341C>T (p.Pro1114Leu)
NM_001278116.2(L1CAM):c.3352G>C (p.Ala1118Pro)
NM_001278116.2(L1CAM):c.3427A>G (p.Ile1143Val)
NM_001278116.2(L1CAM):c.3473A>G (p.Asp1158Gly)
NM_001278116.2(L1CAM):c.3476C>T (p.Thr1159Ile)	rs2064682571
NM_001278116.2(L1CAM):c.3500C>T (p.Pro1167Leu)	rs2064682269
NM_001278116.2(L1CAM):c.3550G>A (p.Glu1184Lys)	rs1557089371
NM_001278116.2(L1CAM):c.3583C>G (p.Leu1195Val)
NM_001278116.2(L1CAM):c.3587A>G (p.Asn1196Ser)	rs2148492028
NM_001278116.2(L1CAM):c.3592G>C (p.Asp1198His)	rs1557089353
NM_001278116.2(L1CAM):c.3613G>A (p.Asp1205Asn)
NM_001278116.2(L1CAM):c.407C>T (p.Pro136Leu)
NM_001278116.2(L1CAM):c.452G>A (p.Gly151Glu)	rs1064796291
NM_001278116.2(L1CAM):c.457T>A (p.Ser153Thr)	rs2148499026
NM_001278116.2(L1CAM):c.595C>T (p.Leu199Phe)
NM_001278116.2(L1CAM):c.641C>T (p.Pro214Leu)
NM_001278116.2(L1CAM):c.707T>C (p.Ile236Thr)
NM_001278116.2(L1CAM):c.76+4A>T	rs2148502509
NM_001278116.2(L1CAM):c.769G>A (p.Gly257Arg)	rs2148498281
NM_001278116.2(L1CAM):c.895C>A (p.Leu299Met)
NM_001278116.2(L1CAM):c.985G>A (p.Val329Met)	rs2148497835

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