ClinVar Miner

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

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Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_004082.5(DCTN1):c.3610-20C>G rs2268427 0.09345
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.2448A>G (p.Ala816=) rs1130484 0.01851
NM_004082.5(DCTN1):c.1484G>A (p.Arg495Gln) rs17721059 0.01316
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.2805C>G (p.Ile935Met) rs145130328 0.00029
NM_004082.5(DCTN1):c.558G>A (p.Pro186=) rs201078804 0.00028
NM_004082.5(DCTN1):c.837G>A (p.Ala279=) rs72466489 0.00020
NM_004082.5(DCTN1):c.2019C>T (p.Ala673=) rs372482596 0.00016
NM_004082.5(DCTN1):c.3501C>T (p.His1167=) rs569997015 0.00012
NM_004082.5(DCTN1):c.1997C>T (p.Thr666Met) rs143914684 0.00010
NM_004082.5(DCTN1):c.3212-10G>A rs201516838 0.00010
NM_004082.5(DCTN1):c.159C>T (p.Ala53=) rs759530214 0.00005
NM_004082.5(DCTN1):c.2952C>G (p.Ala984=) rs371241720 0.00004
NM_004082.5(DCTN1):c.442C>T (p.Arg148Trp) rs148810193 0.00003
NM_004082.5(DCTN1):c.1288-9G>A rs201425449 0.00002
NM_004082.5(DCTN1):c.3699+16G>A rs747490958 0.00002
NM_004082.5(DCTN1):c.2679C>T (p.Cys893=) rs1253918840 0.00001
NM_004082.5(DCTN1):c.3123C>G (p.Ser1041=) rs769629500 0.00001
NM_004082.5(DCTN1):c.3621C>T (p.Leu1207=) rs1032786897 0.00001
NM_004082.5(DCTN1):c.42C>T (p.Ser14=) rs535554555 0.00001
NM_004082.5(DCTN1):c.876C>T (p.Arg292=) rs762389920 0.00001
NM_004082.5(DCTN1):c.1122G>C (p.Leu374=) rs1573162746
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+185G>T rs189187061
NM_004082.5(DCTN1):c.1455G>A (p.Leu485=)
NM_004082.5(DCTN1):c.1500G>A (p.Gln500=) rs1573159627
NM_004082.5(DCTN1):c.1530T>G (p.Val510=)
NM_004082.5(DCTN1):c.2112A>G (p.Glu704=) rs2103630069
NM_004082.5(DCTN1):c.2432C>G (p.Pro811Arg) rs150928856
NM_004082.5(DCTN1):c.2535A>C (p.Ala845=) rs1573152114
NM_004082.5(DCTN1):c.2583A>G (p.Leu861=) rs2104415066
NM_004082.5(DCTN1):c.2769G>A (p.Pro923=)
NM_004082.5(DCTN1):c.280-34_280-12dup rs762313810
NM_004082.5(DCTN1):c.2835C>T (p.Leu945=) rs138305126
NM_004082.5(DCTN1):c.2982C>G (p.Val994=)
NM_004082.5(DCTN1):c.3492A>G (p.Thr1164=) rs1197164602
NM_004082.5(DCTN1):c.3516T>G (p.Thr1172=)
NM_004082.5(DCTN1):c.3700-47C>G rs114222011
NM_004082.5(DCTN1):c.3753A>C (p.Ser1251=)
NM_004082.5(DCTN1):c.3799G>A (p.Glu1267Lys) rs146083590
NM_004082.5(DCTN1):c.627G>T (p.Pro209=) rs147673066
NM_004082.5(DCTN1):c.858G>C (p.Ala286=) rs151107870
NM_004082.5(DCTN1):c.999C>G (p.Asp333Glu) rs200952455

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