ClinVar Miner

List of variants in gene TSEN54 reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 150
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HGVS dbSNP gnomAD frequency
NM_207346.3(TSEN54):c.83C>T (p.Ser28Leu) rs201089582 0.00116
NM_207346.3(TSEN54):c.766G>A (p.Gly256Ser) rs200015685 0.00049
NM_207346.3(TSEN54):c.1114G>A (p.Val372Met) rs200434678 0.00045
NM_207346.3(TSEN54):c.537G>A (p.Pro179=) rs113016401 0.00044
NM_207346.3(TSEN54):c.1313G>A (p.Arg438Gln) rs200228117 0.00041
NM_207346.3(TSEN54):c.1136G>A (p.Arg379Gln) rs201948434 0.00038
NM_207346.3(TSEN54):c.984T>C (p.Ala328=) rs776960594 0.00028
NM_207346.3(TSEN54):c.1063C>T (p.His355Tyr) rs727504183 0.00024
NM_207346.3(TSEN54):c.1079C>T (p.Ala360Val) rs368377822 0.00019
NM_207346.3(TSEN54):c.827G>T (p.Gly276Val) rs777546135 0.00018
NM_207346.3(TSEN54):c.623+4A>G rs1346057234 0.00016
NM_207346.3(TSEN54):c.991G>A (p.Glu331Lys) rs773368581 0.00016
NM_207346.3(TSEN54):c.622C>T (p.Arg208Trp) rs147165460 0.00015
NM_207346.3(TSEN54):c.946C>T (p.Arg316Cys) rs377207901 0.00014
NM_207346.3(TSEN54):c.1057C>T (p.Arg353Trp) rs200540627 0.00013
NM_207346.3(TSEN54):c.437C>A (p.Thr146Asn) rs201623351 0.00013
NM_207346.3(TSEN54):c.753G>T (p.Met251Ile) rs375386151 0.00012
NM_207346.3(TSEN54):c.1252+6C>T rs977124000 0.00010
NM_207346.3(TSEN54):c.1173G>C (p.Gln391His) rs577958629 0.00009
NM_207346.3(TSEN54):c.668C>T (p.Pro223Leu) rs767591488 0.00008
NM_207346.3(TSEN54):c.1035G>C (p.Lys345Asn) rs376308638 0.00007
NM_207346.3(TSEN54):c.468+8C>T rs117456384 0.00007
NM_207346.3(TSEN54):c.881G>A (p.Arg294Gln) rs150805182 0.00006
NM_207346.3(TSEN54):c.1430+5G>A rs367823640 0.00005
NM_207346.3(TSEN54):c.709C>T (p.Pro237Ser) rs745470927 0.00005
NM_207346.3(TSEN54):c.802C>T (p.Pro268Ser) rs757862450 0.00005
NM_207346.3(TSEN54):c.988C>T (p.Arg330Trp) rs748429211 0.00005
NM_207346.3(TSEN54):c.153G>C (p.Gln51His) rs755967065 0.00004
NM_207346.3(TSEN54):c.1088A>G (p.Gln363Arg) rs371709232 0.00003
NM_207346.3(TSEN54):c.1181A>G (p.Gln394Arg) rs560589823 0.00003
NM_207346.3(TSEN54):c.1415G>A (p.Arg472Gln) rs151332020 0.00003
NM_207346.3(TSEN54):c.1469G>A (p.Arg490Gln) rs141950888 0.00003
NM_207346.3(TSEN54):c.176G>A (p.Arg59Gln) rs886043563 0.00003
NM_207346.3(TSEN54):c.587G>A (p.Gly196Glu) rs377382148 0.00003
NM_207346.3(TSEN54):c.1159C>T (p.Arg387Trp) rs941059094 0.00002
NM_207346.3(TSEN54):c.370-2A>G rs762922379 0.00002
NM_207346.3(TSEN54):c.851C>T (p.Ala284Val) rs1298711128 0.00002
NM_207346.3(TSEN54):c.914A>G (p.Asn305Ser) rs776796485 0.00002
NM_207346.3(TSEN54):c.989G>A (p.Arg330Gln) rs769945102 0.00002
NM_207346.3(TSEN54):c.1000G>A (p.Ala334Thr) rs886042169 0.00001
NM_207346.3(TSEN54):c.1078G>A (p.Ala360Thr) rs374200799 0.00001
NM_207346.3(TSEN54):c.1135C>T (p.Arg379Trp) rs761392770 0.00001
NM_207346.3(TSEN54):c.1186C>T (p.Arg396Trp) rs542013784 0.00001
NM_207346.3(TSEN54):c.1276G>A (p.Val426Met) rs747473434 0.00001
NM_207346.3(TSEN54):c.1527C>T (p.Asp509=) rs201415896 0.00001
NM_207346.3(TSEN54):c.1552T>C (p.Phe518Leu) rs749096965 0.00001
NM_207346.3(TSEN54):c.158A>G (p.Glu53Gly) rs1180659663 0.00001
NM_207346.3(TSEN54):c.181G>A (p.Glu61Lys) rs1438493791 0.00001
NM_207346.3(TSEN54):c.195G>A (p.Leu65=) rs768783066 0.00001
NM_207346.3(TSEN54):c.197T>C (p.Leu66Pro) rs1388222262 0.00001
NM_207346.3(TSEN54):c.200C>T (p.Ala67Val) rs1326441166 0.00001
NM_207346.3(TSEN54):c.277T>C (p.Ser93Pro) rs113994151 0.00001
NM_207346.3(TSEN54):c.278C>T (p.Ser93Phe) rs1289867668 0.00001
NM_207346.3(TSEN54):c.284C>T (p.Ala95Val) rs1385660656 0.00001
NM_207346.3(TSEN54):c.367T>A (p.Cys123Ser) rs1484028244 0.00001
NM_207346.3(TSEN54):c.394G>A (p.Asp132Asn) rs750942705 0.00001
NM_207346.3(TSEN54):c.506G>A (p.Arg169Gln) rs768076552 0.00001
NM_207346.3(TSEN54):c.745A>C (p.Ser249Arg) rs761784110 0.00001
NM_207346.3(TSEN54):c.909C>G (p.Phe303Leu) rs199874361 0.00001
NM_207346.3(TSEN54):c.932G>A (p.Arg311His) rs773833320 0.00001
NM_207346.3(TSEN54):c.949G>A (p.Ala317Thr) rs201125812 0.00001
NM_207346.3(TSEN54):c.964C>G (p.Leu322Val) rs587784480 0.00001
NM_207346.3(TSEN54):c.1028A>C (p.Gln343Pro) rs994403512
NM_207346.3(TSEN54):c.1039_1041delinsTAC (p.Lys347Tyr) rs1568003520
NM_207346.3(TSEN54):c.1052G>A (p.Arg351Gln)
NM_207346.3(TSEN54):c.1060G>C (p.Glu354Gln)
NM_207346.3(TSEN54):c.1061A>G (p.Glu354Gly)
NM_207346.3(TSEN54):c.1062_1091del (p.His355_Glu364del)
NM_207346.3(TSEN54):c.1064A>G (p.His355Arg)
NM_207346.3(TSEN54):c.1068C>A (p.His356Gln)
NM_207346.3(TSEN54):c.1078G>C (p.Ala360Pro)
NM_207346.3(TSEN54):c.1091A>G (p.Glu364Gly)
NM_207346.3(TSEN54):c.1105G>A (p.Asp369Asn)
NM_207346.3(TSEN54):c.1107_1112dup (p.Pro370_Glu371insAspPro)
NM_207346.3(TSEN54):c.110C>G (p.Ser37Trp)
NM_207346.3(TSEN54):c.1111G>A (p.Glu371Lys) rs398124621
NM_207346.3(TSEN54):c.1120_1122delinsGGC (p.Arg374Gly) rs1555644694
NM_207346.3(TSEN54):c.1121G>A (p.Arg374Gln)
NM_207346.3(TSEN54):c.1130G>T (p.Ser377Ile)
NM_207346.3(TSEN54):c.1160G>A (p.Arg387Gln) rs1055536776
NM_207346.3(TSEN54):c.1162C>T (p.Arg388Trp)
NM_207346.3(TSEN54):c.1163G>C (p.Arg388Pro) rs796181199
NM_207346.3(TSEN54):c.1175G>C (p.Arg392Thr)
NM_207346.3(TSEN54):c.1183C>G (p.Arg395Gly) rs572964665
NM_207346.3(TSEN54):c.1187G>A (p.Arg396Gln)
NM_207346.3(TSEN54):c.1190C>T (p.Ala397Val)
NM_207346.3(TSEN54):c.1239G>C (p.Gln413His) rs2147013922
NM_207346.3(TSEN54):c.1270A>G (p.Ile424Val)
NM_207346.3(TSEN54):c.1294C>T (p.Leu432Phe)
NM_207346.3(TSEN54):c.1300G>C (p.Asp434His)
NM_207346.3(TSEN54):c.1309_1310delinsAT (p.Ala437Ile) rs2147015701
NM_207346.3(TSEN54):c.1372G>A (p.Val458Met)
NM_207346.3(TSEN54):c.1388A>C (p.Lys463Thr)
NM_207346.3(TSEN54):c.1414C>T (p.Arg472Trp)
NM_207346.3(TSEN54):c.1419G>A (p.Met473Ile)
NM_207346.3(TSEN54):c.1429G>A (p.Gly477Arg)
NM_207346.3(TSEN54):c.1439A>G (p.Glu480Gly)
NM_207346.3(TSEN54):c.143C>T (p.Ser48Leu) rs1479320072
NM_207346.3(TSEN54):c.145G>A (p.Ala49Thr)
NM_207346.3(TSEN54):c.1462C>G (p.Leu488Val) rs2147019398
NM_207346.3(TSEN54):c.1503C>G (p.Ile501Met)
NM_207346.3(TSEN54):c.151C>G (p.Gln51Glu)
NM_207346.3(TSEN54):c.1520A>G (p.His507Arg)
NM_207346.3(TSEN54):c.1522G>A (p.Gly508Ser) rs2053477029
NM_207346.3(TSEN54):c.1564C>G (p.Gln522Glu)
NM_207346.3(TSEN54):c.1575dup (p.His526fs)
NM_207346.3(TSEN54):c.175C>G (p.Arg59Gly)
NM_207346.3(TSEN54):c.197_198delinsGT (p.Leu66Arg)
NM_207346.3(TSEN54):c.200C>G (p.Ala67Gly)
NM_207346.3(TSEN54):c.211G>A (p.Val71Met)
NM_207346.3(TSEN54):c.221+1G>A rs2147005854
NM_207346.3(TSEN54):c.221+6_221+7del rs2147005865
NM_207346.3(TSEN54):c.222-7T>A rs1555643725
NM_207346.3(TSEN54):c.289A>C (p.Lys97Gln)
NM_207346.3(TSEN54):c.290_292del (p.Lys97_Phe98delinsIle) rs750645536
NM_207346.3(TSEN54):c.302C>G (p.Thr101Ser) rs373908614
NM_207346.3(TSEN54):c.315A>T (p.Ser105=)
NM_207346.3(TSEN54):c.369+4dup
NM_207346.3(TSEN54):c.370-6T>G rs2147007790
NM_207346.3(TSEN54):c.370G>A (p.Gly124Ser) rs770694652
NM_207346.3(TSEN54):c.383T>A (p.Leu128His) rs2147007841
NM_207346.3(TSEN54):c.427C>A (p.Leu143Met)
NM_207346.3(TSEN54):c.536C>G (p.Pro179Arg) rs376310114
NM_207346.3(TSEN54):c.536C>T (p.Pro179Leu) rs376310114
NM_207346.3(TSEN54):c.547C>A (p.Gln183Lys)
NM_207346.3(TSEN54):c.568G>T (p.Val190Leu) rs79508780
NM_207346.3(TSEN54):c.613T>A (p.Ser205Thr)
NM_207346.3(TSEN54):c.614C>T (p.Ser205Phe)
NM_207346.3(TSEN54):c.634AAG[1] (p.Lys213del) rs794727939
NM_207346.3(TSEN54):c.636G>T (p.Lys212Asn) rs2147012981
NM_207346.3(TSEN54):c.688A>G (p.Ser230Gly)
NM_207346.3(TSEN54):c.691C>T (p.Pro231Ser) rs972897786
NM_207346.3(TSEN54):c.707A>G (p.Gln236Arg) rs200904080
NM_207346.3(TSEN54):c.718T>C (p.Cys240Arg)
NM_207346.3(TSEN54):c.734C>T (p.Pro245Leu) rs1276301439
NM_207346.3(TSEN54):c.752T>G (p.Met251Arg)
NM_207346.3(TSEN54):c.802C>G (p.Pro268Ala) rs757862450
NM_207346.3(TSEN54):c.803C>G (p.Pro268Arg) rs2147013200
NM_207346.3(TSEN54):c.806G>C (p.Gly269Ala) rs2147013208
NM_207346.3(TSEN54):c.820G>T (p.Gly274Trp)
NM_207346.3(TSEN54):c.823G>C (p.Val275Leu) rs1040846492
NM_207346.3(TSEN54):c.858C>G (p.Asn286Lys)
NM_207346.3(TSEN54):c.888G>C (p.Trp296Cys)
NM_207346.3(TSEN54):c.901A>G (p.Ile301Val)
NM_207346.3(TSEN54):c.937A>T (p.Thr313Ser)
NM_207346.3(TSEN54):c.946C>G (p.Arg316Gly)
NM_207346.3(TSEN54):c.949G>T (p.Ala317Ser) rs201125812
NM_207346.3(TSEN54):c.959C>G (p.Pro320Arg) rs189860274
NM_207346.3(TSEN54):c.971C>T (p.Pro324Leu)
NM_207346.3(TSEN54):c.977A>C (p.Asn326Thr)

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