ClinVar Miner

List of variants in gene DCTN1 reported as benign for not provided

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Total variants: 48
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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.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.3529+5G>A rs72466494 0.00644
NM_004082.5(DCTN1):c.586A>G (p.Ile196Val) rs55862001 0.00462
NM_004082.5(DCTN1):c.3746C>T (p.Thr1249Ile) rs72466496 0.00287
NM_004082.5(DCTN1):c.3594C>T (p.Thr1198=) rs115689748 0.00250
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.3498G>A (p.Thr1166=) rs142030960 0.00086
NM_004082.5(DCTN1):c.1998G>A (p.Thr666=) rs149900553 0.00061
NM_004082.5(DCTN1):c.2805C>G (p.Ile935Met) rs145130328 0.00029
NM_004082.5(DCTN1):c.40A>G (p.Ser14Gly) rs758320436 0.00010
NM_004082.5(DCTN1):c.3573G>A (p.Gln1191=) rs137966704 0.00009
NM_004082.5(DCTN1):c.3519C>T (p.Arg1173=) rs146094433 0.00002
NM_004082.5(DCTN1):c.1392+148del rs58901202
NM_004082.5(DCTN1):c.1854+139C>T rs34598987
NM_004082.5(DCTN1):c.2432C>G (p.Pro811Arg) rs150928856
NM_004082.5(DCTN1):c.3609+244C>A rs114798160
NM_004082.5(DCTN1):c.3799G>A (p.Glu1267Lys) rs146083590
NM_004082.5(DCTN1):c.415-142_415-140del rs57641394
NM_004082.5(DCTN1):c.415-675A>G rs2075743
NM_004082.5(DCTN1):c.454-147_454-145del rs35914551
NM_004082.5(DCTN1):c.627G>T (p.Pro209=) rs147673066

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