ClinVar Miner

List of variants in gene DCTN1 reported as likely benign for amyotrophic lateral sclerosis type 1

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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NM_004082.4(DCTN1):c.1251C>T (p.Ser417=) rs1553465163
NM_004082.4(DCTN1):c.2205T>G (p.Leu735=) rs773099597
NM_004082.4(DCTN1):c.2217T>G (p.Pro739=) rs1553464448
NM_004082.4(DCTN1):c.2238G>A (p.Leu746=) rs1553464441
NM_004082.4(DCTN1):c.2254-10A>G rs954787850
NM_004082.4(DCTN1):c.2254-5C>T rs746514094
NM_004082.4(DCTN1):c.2544T>C (p.Ala848=) rs1371265373
NM_004082.4(DCTN1):c.288A>G (p.Val96=) rs1553466396
NM_004082.4(DCTN1):c.2952C>G (p.Ala984=) rs371241720
NM_004082.4(DCTN1):c.3069C>T (p.Ile1023=) rs780292959
NM_004082.4(DCTN1):c.3132G>C (p.Thr1044=) rs375157202
NM_004082.4(DCTN1):c.3312C>T (p.Ile1104=) rs777452161
NM_004082.4(DCTN1):c.3597C>T (p.Val1199=) rs767954436
NM_004082.4(DCTN1):c.42C>T (p.Ser14=) rs535554555
NM_004082.4(DCTN1):c.654G>A (p.Glu218=) rs758731839
NM_004082.4(DCTN1):c.759C>T (p.Ile253=) rs1553465355

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