ClinVar Miner

List of variants in gene DCTN1 reported by GeneDx

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Gene type:
ClinVar version:
Total variants: 87
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HGVS dbSNP gnomAD frequency
NM_004082.5(DCTN1):c.1701+56dup rs3216580 0.21850
NM_004082.5(DCTN1):c.359-80G>A rs3213672 0.19555
NM_004082.5(DCTN1):c.3699+160T>C rs741788 0.12053
NM_004082.5(DCTN1):c.2016-23C>T rs909177 0.11913
NM_004082.5(DCTN1):c.1128-55C>T rs740277 0.11747
NM_004082.5(DCTN1):c.280-42A>G rs3815241 0.10342
NM_004082.5(DCTN1):c.3610-20C>G rs2268427 0.09345
NM_004082.5(DCTN1):c.3530-41C>A rs2268426 0.09221
NM_004082.5(DCTN1):c.844-32G>T rs13420292 0.08786
NM_004082.5(DCTN1):c.3610-92C>T rs60453234 0.07664
NM_001190836.2(DCTN1):c.-18-2145T>C rs13411165 0.07636
NM_004082.5(DCTN1):c.1393-22A>C rs13429740 0.07357
NM_004082.5(DCTN1):c.280-34A>T rs13388914 0.06435
NM_004082.5(DCTN1):c.393+103T>G rs72659368 0.04309
NM_004082.5(DCTN1):c.2886+83A>G rs28706943 0.04275
NM_004082.5(DCTN1):c.1393-35C>T rs13416427 0.04269
NM_004082.5(DCTN1):c.3610-65G>A rs61601276 0.04257
NM_004082.5(DCTN1):c.433-259G>A rs56747190 0.04256
NM_004082.5(DCTN1):c.3530-128T>C rs10153548 0.04250
NM_004082.5(DCTN1):c.433-226A>G rs61676484 0.04244
NM_004082.5(DCTN1):c.1605A>G (p.Thr535=) rs13429423 0.04117
NM_004082.5(DCTN1):c.859C>A (p.Leu287Met) rs13420401 0.03855
NM_004082.5(DCTN1):c.1855-225C>T rs2268425 0.02899
NM_004082.5(DCTN1):c.1855-233C>A rs116513775 0.02845
NM_004082.5(DCTN1):c.3610-62G>T rs57084028 0.02813
NM_004082.5(DCTN1):c.454-127T>C rs10179490 0.02201
NM_004082.5(DCTN1):c.2448A>G (p.Ala816=) rs1130484 0.01851
NM_004082.5(DCTN1):c.1484G>A (p.Arg495Gln) rs17721059 0.01316
NM_004082.5(DCTN1):c.1288-3C>T rs72466490 0.01285
NM_004082.5(DCTN1):c.34-11G>T rs73948789 0.01216
NM_004082.5(DCTN1):c.1701+82G>T rs112487792 0.00769
NM_004082.5(DCTN1):c.1854+52A>G rs56943021 0.00721
NM_004082.5(DCTN1):c.393+152T>C rs72659369 0.00678
NM_004082.5(DCTN1):c.3529+5G>A rs72466494 0.00644
NM_004082.5(DCTN1):c.3197-21C>G rs60419532 0.00627
NM_004082.5(DCTN1):c.586A>G (p.Ile196Val) rs55862001 0.00462
NM_004082.5(DCTN1):c.1855-143C>T rs116081661 0.00349
NM_004082.5(DCTN1):c.3746C>T (p.Thr1249Ile) rs72466496 0.00287
NM_004082.5(DCTN1):c.3146G>A (p.Arg1049Gln) rs72659383 0.00166
NM_004082.5(DCTN1):c.280-3C>T rs114364621 0.00094
NM_004082.5(DCTN1):c.2805C>G (p.Ile935Met) rs145130328 0.00029
NM_004082.5(DCTN1):c.1997C>T (p.Thr666Met) rs143914684 0.00010
NM_004082.5(DCTN1):c.100G>C (p.Glu34Gln) rs151052060 0.00008
NM_004082.5(DCTN1):c.3010C>G (p.Leu1004Val) rs758387062 0.00006
NM_004082.5(DCTN1):c.2647A>T (p.Ser883Cys) rs747769504 0.00004
NM_004082.5(DCTN1):c.3640C>T (p.Arg1214Cys) rs759373031 0.00004
NM_004082.5(DCTN1):c.673C>T (p.Arg225Trp) rs371723224 0.00004
NM_004082.5(DCTN1):c.824G>A (p.Arg275His) rs375266113 0.00004
NM_004082.5(DCTN1):c.439A>G (p.Thr147Ala) rs371437767 0.00003
NM_004082.5(DCTN1):c.2244C>G (p.Asp748Glu) rs751069902 0.00002
NM_004082.5(DCTN1):c.1238A>G (p.Gln413Arg) rs745458066 0.00001
NM_004082.5(DCTN1):c.1523A>G (p.Glu508Gly) rs148449665 0.00001
NM_004082.5(DCTN1):c.2511C>T (p.Val837=) rs377519506 0.00001
NM_004082.5(DCTN1):c.427C>T (p.Arg143Ter) rs781290307 0.00001
NM_004082.5(DCTN1):c.521C>T (p.Ser174Leu) rs1064797035 0.00001
NM_004082.5(DCTN1):c.557C>T (p.Pro186Leu) rs916359967 0.00001
NM_004082.5(DCTN1):c.1060G>T (p.Ala354Ser) rs1350015363
NM_004082.5(DCTN1):c.1061C>G (p.Ala354Gly)
NM_004082.5(DCTN1):c.1392+129_1392+130dup rs58901202
NM_004082.5(DCTN1):c.1392+129_1392+131dup rs58901202
NM_004082.5(DCTN1):c.1392+148del rs58901202
NM_004082.5(DCTN1):c.1392+185G>T rs189187061
NM_004082.5(DCTN1):c.1504C>T (p.Arg502Cys) rs145958900
NM_004082.5(DCTN1):c.156T>G (p.Phe52Leu) rs886039227
NM_004082.5(DCTN1):c.1719G>T (p.Leu573Phe)
NM_004082.5(DCTN1):c.1854+139C>T rs34598987
NM_004082.5(DCTN1):c.1915C>T (p.Arg639Trp)
NM_004082.5(DCTN1):c.200G>T (p.Gly67Val) rs886039228
NM_004082.5(DCTN1):c.2427T>G (p.Asp809Glu) rs1573152954
NM_004082.5(DCTN1):c.2653C>A (p.Pro885Thr)
NM_004082.5(DCTN1):c.2680A>G (p.Asn894Asp) rs1437825772
NM_004082.5(DCTN1):c.2785G>A (p.Ala929Thr)
NM_004082.5(DCTN1):c.279+1G>T rs1393363759
NM_004082.5(DCTN1):c.279G>C (p.Gln93His)
NM_004082.5(DCTN1):c.2986A>G (p.Thr996Ala) rs1558935430
NM_004082.5(DCTN1):c.3293C>T (p.Ser1098Phe)
NM_004082.5(DCTN1):c.3609+244C>A rs114798160
NM_004082.5(DCTN1):c.3659C>A (p.Pro1220His) rs1276978486
NM_004082.5(DCTN1):c.3700-47C>G rs114222011
NM_004082.5(DCTN1):c.3799G>A (p.Glu1267Lys) rs146083590
NM_004082.5(DCTN1):c.394-12C>G
NM_004082.5(DCTN1):c.415-142_415-140del rs57641394
NM_004082.5(DCTN1):c.415-675A>G rs2075743
NM_004082.5(DCTN1):c.432+1G>T rs1235693710
NM_004082.5(DCTN1):c.454-147_454-145del rs35914551
NM_004082.5(DCTN1):c.575C>T (p.Ala192Val)
NM_004082.5(DCTN1):c.627G>T (p.Pro209=) rs147673066

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