ClinVar Miner

List of variants in gene VCL studied for not provided

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Gene type:
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Total variants: 103
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HGVS dbSNP
NC_000010.11:g.74083685_74083688del
NM_014000.2(VCL):c.-264A>G
NM_014000.2(VCL):c.-386A>G
NM_014000.2(VCL):c.1015C>T (p.Arg339Cys) rs759961842
NM_014000.2(VCL):c.1157A>G (p.Lys386Arg) rs200342284
NM_014000.2(VCL):c.1177-158_1177-157insCA
NM_014000.2(VCL):c.1192C>T (p.Pro398Ser) rs201528612
NM_014000.2(VCL):c.1195A>C (p.Asn399His) rs377228795
NM_014000.2(VCL):c.1198G>T (p.Gly400Cys) rs201361282
NM_014000.2(VCL):c.1225C>T (p.Arg409Ter) rs202005455
NM_014000.2(VCL):c.1229G>A (p.Gly410Asp) rs1064796607
NM_014000.2(VCL):c.1237G>A (p.Ala413Thr) rs146278697
NM_014000.2(VCL):c.1238C>T (p.Ala413Val) rs794729190
NM_014000.2(VCL):c.1292T>G (p.Ile431Ser) rs766192312
NM_014000.2(VCL):c.1294C>G (p.Leu432Val) rs144146254
NM_014000.2(VCL):c.1297C>T (p.Arg433Cys) rs139559937
NM_014000.2(VCL):c.1298G>A (p.Arg433His) rs754046223
NM_014000.2(VCL):c.1346G>A (p.Arg449Gln) rs755234443
NM_014000.2(VCL):c.1353-233C>T
NM_014000.2(VCL):c.1403C>T (p.Thr468Met) rs147957747
NM_014000.2(VCL):c.1535G>A (p.Arg512His) rs367568441
NM_014000.2(VCL):c.1542C>T (p.Val514=) rs7904077
NM_014000.2(VCL):c.1555A>C (p.Ile519Leu) rs141033098
NM_014000.2(VCL):c.1583G>A (p.Arg528His) rs746095066
NM_014000.2(VCL):c.1607C>A (p.Pro536His) rs200624351
NM_014000.2(VCL):c.1626C>T (p.Leu542=) rs150402791
NM_014000.2(VCL):c.1652T>C (p.Leu551Pro) rs1057524278
NM_014000.2(VCL):c.1671C>T (p.Asp557=) rs137877092
NM_014000.2(VCL):c.169-290A>G
NM_014000.2(VCL):c.1708C>T (p.Arg570Ter) rs794729191
NM_014000.2(VCL):c.1743+229C>T
NM_014000.2(VCL):c.1744-1G>T rs1057524654
NM_014000.2(VCL):c.1788A>C (p.Ser596=) rs199582103
NM_014000.2(VCL):c.1798A>C (p.Ser600Arg) rs397517236
NM_014000.2(VCL):c.1819A>C (p.Lys607Gln) rs794729192
NM_014000.2(VCL):c.1863C>G (p.Asn621Lys) rs746293391
NM_014000.2(VCL):c.1872+197G>C
NM_014000.2(VCL):c.1872+199A>C
NM_014000.2(VCL):c.1907A>G (p.His636Arg) rs71579374
NM_014000.2(VCL):c.1928C>T (p.Thr643Met) rs150643310
NM_014000.2(VCL):c.1940C>T (p.Ala647Val) rs534449109
NM_014000.2(VCL):c.2000C>T (p.Thr667Met) rs794729187
NM_014000.2(VCL):c.2022+167C>T
NM_014000.2(VCL):c.2050A>T (p.Arg684Trp) rs730880249
NM_014000.2(VCL):c.2069C>A (p.Ala690Asp) rs1057524826
NM_014000.2(VCL):c.2131+64C>T
NM_014000.2(VCL):c.2237C>A (p.Pro746His) rs746821947
NM_014000.2(VCL):c.224C>T (p.Pro75Leu) rs373830664
NM_014000.2(VCL):c.2267T>C (p.Ile756Thr) rs1554818898
NM_014000.2(VCL):c.2365G>A (p.Glu789Lys) rs745419923
NM_014000.2(VCL):c.2387C>T (p.Pro796Leu) rs1364541925
NM_014000.2(VCL):c.238A>C (p.Lys80Gln) rs775532257
NM_014000.2(VCL):c.2428G>A (p.Asp810Asn) rs751458490
NM_014000.2(VCL):c.2434+159G>A
NM_014000.2(VCL):c.2434+48C>T
NM_014000.2(VCL):c.2435-1G>A rs794729188
NM_014000.2(VCL):c.2435-59C>A
NM_014000.2(VCL):c.2453T>A (p.Leu818Gln) rs794727192
NM_014000.2(VCL):c.248A>T (p.Asn83Ile) rs1554816646
NM_014000.2(VCL):c.2521G>C (p.Asp841His) rs150385900
NM_014000.2(VCL):c.2528C>T (p.Pro843Leu) rs764302249
NM_014000.2(VCL):c.2539C>T (p.Pro847Ser) rs372711612
NM_014000.2(VCL):c.2559+18T>C
NM_014000.2(VCL):c.2652G>A (p.Glu884=) rs371187988
NM_014000.2(VCL):c.2745+151T>C
NM_014000.2(VCL):c.2760C>T (p.Ala920=)
NM_014000.2(VCL):c.2801C>T (p.Ala934Val) rs16931179
NM_014000.2(VCL):c.2823_2824delinsGT (p.Pro942Ser) rs1060502196
NM_014000.2(VCL):c.2827C>G (p.Pro943Ala) rs71579375
NM_014000.2(VCL):c.2828_2829del (p.Pro943fs) rs781036800
NM_014000.2(VCL):c.2852C>G (p.Pro951Arg) rs368570586
NM_014000.2(VCL):c.2862_2864del (p.Leu955del) rs397517237
NM_014000.2(VCL):c.2893C>T (p.Pro965Ser) rs749236817
NM_014000.2(VCL):c.2905G>A (p.Ala969Thr) rs199751261
NM_014000.2(VCL):c.292G>A (p.Asp98Asn) rs794729193
NM_014000.2(VCL):c.2950-22C>G
NM_014000.2(VCL):c.2950-50C>T
NM_014000.2(VCL):c.2969C>T (p.Ala990Val) rs150595117
NM_014000.2(VCL):c.3008G>A (p.Arg1003Gln) rs1085307604
NM_014000.2(VCL):c.3019G>C (p.Gly1007Arg) rs1554819630
NM_014000.2(VCL):c.3163C>T (p.Arg1055Ter) rs727505159
NM_014000.2(VCL):c.32G>A (p.Ser11Asn) rs777811020
NM_014000.2(VCL):c.379G>A (p.Asp127Asn) rs1554816666
NM_014000.2(VCL):c.404T>C (p.Ile135Thr) rs373744314
NM_014000.2(VCL):c.500-236A>G
NM_014000.2(VCL):c.500-281T>C
NM_014000.2(VCL):c.50C>A (p.Ala17Glu) rs794729189
NM_014000.2(VCL):c.562C>T (p.Arg188Ter) rs397517244
NM_014000.2(VCL):c.565G>T (p.Val189Leu) rs151045204
NM_014000.2(VCL):c.571T>C (p.Leu191=)
NM_014000.2(VCL):c.590C>T (p.Thr197Ile) rs189242810
NM_014000.2(VCL):c.610G>C (p.Val204Leu) rs727504585
NM_014000.2(VCL):c.622+158G>A
NM_014000.2(VCL):c.622+191C>T
NM_014000.2(VCL):c.622+211T>C
NM_014000.2(VCL):c.623-83T>C
NM_014000.2(VCL):c.676G>A (p.Ala226Thr) rs146910007
NM_014000.2(VCL):c.688C>T (p.Arg230Cys) rs139312390
NM_014000.2(VCL):c.695T>A (p.Phe232Tyr) rs200956572
NM_014000.2(VCL):c.736C>T (p.Arg246Cys) rs794729194
NM_014000.2(VCL):c.784-60G>A
NM_014000.2(VCL):c.875-24T>A rs1908339
NM_014000.2(VCL):c.875-324dup

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