ClinVar Miner

List of variants in gene DCTN1 reported as uncertain significance for amyotrophic lateral sclerosis type 1

Included ClinVar conditions (2):
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ClinVar version:
Total variants: 126
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HGVS dbSNP
NM_004082.4(DCTN1):c.1102G>A (p.Ala368Thr) rs1034996844
NM_004082.4(DCTN1):c.1127+6G>A rs951022782
NM_004082.4(DCTN1):c.1128-3C>G
NM_004082.4(DCTN1):c.1129A>C (p.Met377Leu) rs570863800
NM_004082.4(DCTN1):c.1217G>A (p.Arg406Lys) rs1040712616
NM_004082.4(DCTN1):c.1225C>T (p.Arg409Trp)
NM_004082.4(DCTN1):c.1255G>A (p.Ala419Thr) rs922032527
NM_004082.4(DCTN1):c.1288-10C>G
NM_004082.4(DCTN1):c.1288-6A>G rs1236101222
NM_004082.4(DCTN1):c.1316T>C (p.Met439Thr)
NM_004082.4(DCTN1):c.1324A>G (p.Met442Val) rs763480310
NM_004082.4(DCTN1):c.1364G>A (p.Arg455His) rs763277715
NM_004082.4(DCTN1):c.1388A>G (p.Asp463Gly) rs1558941192
NM_004082.4(DCTN1):c.1393-7G>A
NM_004082.4(DCTN1):c.142_143delinsAT (p.Gly48Ile)
NM_004082.4(DCTN1):c.1430A>G (p.Asn477Ser)
NM_004082.4(DCTN1):c.1435C>T (p.Arg479Cys) rs1558940606
NM_004082.4(DCTN1):c.1481C>T (p.Ala494Val)
NM_004082.4(DCTN1):c.1486G>C (p.Val496Leu)
NM_004082.4(DCTN1):c.1526C>T (p.Thr509Met)
NM_004082.4(DCTN1):c.1584+5A>G
NM_004082.4(DCTN1):c.1595G>A (p.Arg532Gln) rs759306485
NM_004082.4(DCTN1):c.1606A>C (p.Asn536His) rs1553464927
NM_004082.4(DCTN1):c.167A>G (p.Lys56Arg) rs566433112
NM_004082.4(DCTN1):c.1706T>A (p.Ile569Asn) rs1553464828
NM_004082.4(DCTN1):c.1752C>A (p.His584Gln) rs1345909454
NM_004082.4(DCTN1):c.1780G>C (p.Asp594His)
NM_004082.4(DCTN1):c.1784G>A (p.Ser595Asn) rs1243051229
NM_004082.4(DCTN1):c.1793G>A (p.Arg598Gln)
NM_004082.4(DCTN1):c.1807C>A (p.His603Asn) rs1558939544
NM_004082.4(DCTN1):c.1816G>A (p.Val606Ile) rs375778151
NM_004082.4(DCTN1):c.1928G>A (p.Arg643Gln) rs555733849
NM_004082.4(DCTN1):c.1936G>T (p.Ala646Ser)
NM_004082.4(DCTN1):c.1997C>T (p.Thr666Met) rs143914684
NM_004082.4(DCTN1):c.2002C>T (p.His668Tyr) rs764443534
NM_004082.4(DCTN1):c.2005C>T (p.Arg669Cys) rs150746209
NM_004082.4(DCTN1):c.2006G>A (p.Arg669His)
NM_004082.4(DCTN1):c.2016-6C>A
NM_004082.4(DCTN1):c.2083C>T (p.His695Tyr)
NM_004082.4(DCTN1):c.2209G>A (p.Glu737Lys) rs377183051
NM_004082.4(DCTN1):c.2278A>G (p.Met760Val) rs754780894
NM_004082.4(DCTN1):c.2290G>A (p.Val764Ile) rs753618444
NM_004082.4(DCTN1):c.232T>C (p.Tyr78His) rs1558948987
NM_004082.4(DCTN1):c.2339T>C (p.Ile780Thr) rs374163967
NM_004082.4(DCTN1):c.2353C>T (p.Arg785Trp) rs121909344
NM_004082.4(DCTN1):c.2357A>G (p.Asp786Gly) rs752889408
NM_004082.4(DCTN1):c.2384G>A (p.Arg795His)
NM_004082.4(DCTN1):c.2411G>A (p.Arg804Gln)
NM_004082.4(DCTN1):c.2427T>G (p.Asp809Glu)
NM_004082.4(DCTN1):c.2467G>A (p.Val823Ile)
NM_004082.4(DCTN1):c.2477C>T (p.Thr826Met) rs766585070
NM_004082.4(DCTN1):c.2480T>C (p.Leu827Pro) rs1470946965
NM_004082.4(DCTN1):c.2540C>G (p.Ala847Gly)
NM_004082.4(DCTN1):c.2551C>G (p.Leu851Val)
NM_004082.4(DCTN1):c.2629-7C>A rs1278207608
NM_004082.4(DCTN1):c.2633A>G (p.Tyr878Cys) rs778201974
NM_004082.4(DCTN1):c.2647A>T (p.Ser883Cys) rs747769504
NM_004082.4(DCTN1):c.2731dup (p.Glu911fs)
NM_004082.4(DCTN1):c.2747G>A (p.Arg916Gln) rs375079576
NM_004082.4(DCTN1):c.2779C>T (p.Arg927Trp)
NM_004082.4(DCTN1):c.279+1G>T rs1393363759
NM_004082.4(DCTN1):c.2836G>A (p.Glu946Lys)
NM_004082.4(DCTN1):c.2872T>G (p.Ser958Ala)
NM_004082.4(DCTN1):c.2879A>G (p.Lys960Arg)
NM_004082.4(DCTN1):c.2883T>G (p.Ile961Met)
NM_004082.4(DCTN1):c.2909A>G (p.Asn970Ser) rs568812456
NM_004082.4(DCTN1):c.2974G>A (p.Glu992Lys) rs768409522
NM_004082.4(DCTN1):c.2986A>G (p.Thr996Ala) rs1558935430
NM_004082.4(DCTN1):c.3017G>A (p.Arg1006Gln) rs752882353
NM_004082.4(DCTN1):c.3029+6G>T rs754143116
NM_004082.4(DCTN1):c.3127C>T (p.Arg1043Cys) rs140066692
NM_004082.4(DCTN1):c.3128G>A (p.Arg1043His) rs776489779
NM_004082.4(DCTN1):c.3137A>G (p.Glu1046Gly) rs145857843
NM_004082.4(DCTN1):c.3158C>T (p.Pro1053Leu)
NM_004082.4(DCTN1):c.3172A>T (p.Thr1058Ser)
NM_004082.4(DCTN1):c.3199G>T (p.Glu1067Ter) rs376996779
NM_004082.4(DCTN1):c.3215C>G (p.Ala1072Gly) rs780875333
NM_004082.4(DCTN1):c.3217A>G (p.Ile1073Val)
NM_004082.4(DCTN1):c.3241G>A (p.Val1081Met) rs764028925
NM_004082.4(DCTN1):c.3254G>A (p.Gly1085Glu) rs1274754432
NM_004082.4(DCTN1):c.3382C>G (p.Pro1128Ala)
NM_004082.4(DCTN1):c.3425A>G (p.Glu1142Gly)
NM_004082.4(DCTN1):c.3449G>A (p.Arg1150His) rs771822061
NM_004082.4(DCTN1):c.3533C>T (p.Ala1178Val) rs775442446
NM_004082.4(DCTN1):c.3545C>T (p.Ser1182Leu)
NM_004082.4(DCTN1):c.3556A>G (p.Met1186Val) rs1477782343
NM_004082.4(DCTN1):c.3557T>C (p.Met1186Thr) rs145819459
NM_004082.4(DCTN1):c.3643C>T (p.Pro1215Ser)
NM_004082.4(DCTN1):c.3652A>G (p.Thr1218Ala) rs886070472
NM_004082.4(DCTN1):c.3712C>G (p.Gln1238Glu)
NM_004082.4(DCTN1):c.3728T>C (p.Val1243Ala)
NM_004082.4(DCTN1):c.3759G>A (p.Ala1253=) rs886056328
NM_004082.4(DCTN1):c.3760G>T (p.Ala1254Ser)
NM_004082.4(DCTN1):c.376G>A (p.Ala126Thr) rs1553466338
NM_004082.4(DCTN1):c.3776G>A (p.Arg1259Gln)
NM_004082.4(DCTN1):c.3778C>T (p.His1260Tyr) rs1375787578
NM_004082.4(DCTN1):c.3781C>T (p.Arg1261Trp)
NM_004082.4(DCTN1):c.3803A>G (p.Gln1268Arg) rs751431467
NM_004082.4(DCTN1):c.3824G>A (p.Arg1275His) rs560344779
NM_004082.4(DCTN1):c.40A>G (p.Ser14Gly) rs758320436
NM_004082.4(DCTN1):c.414+1G>A rs576198476
NM_004082.4(DCTN1):c.419C>T (p.Pro140Leu) rs147939455
NM_004082.4(DCTN1):c.424G>C (p.Ala142Pro)
NM_004082.4(DCTN1):c.427C>T (p.Arg143Ter) rs781290307
NM_004082.4(DCTN1):c.439A>G (p.Thr147Ala) rs371437767
NM_004082.4(DCTN1):c.442C>T (p.Arg148Trp) rs148810193
NM_004082.4(DCTN1):c.446G>A (p.Arg149Gln) rs149447433
NM_004082.4(DCTN1):c.458C>T (p.Thr153Met)
NM_004082.4(DCTN1):c.45C>T (p.Gly15=)
NM_004082.4(DCTN1):c.460C>T (p.Arg154Cys) rs141670992
NM_004082.4(DCTN1):c.557C>T (p.Pro186Leu) rs916359967
NM_004082.4(DCTN1):c.559G>T (p.Ala187Ser) rs960727301
NM_004082.4(DCTN1):c.569C>T (p.Pro190Leu) rs765192491
NM_004082.4(DCTN1):c.59C>T (p.Ala20Val) rs773420384
NM_004082.4(DCTN1):c.626C>T (p.Pro209Leu) rs112725508
NM_004082.4(DCTN1):c.629T>G (p.Leu210Arg) rs1558943273
NM_004082.4(DCTN1):c.638C>T (p.Pro213Leu) rs754827026
NM_004082.4(DCTN1):c.673C>T (p.Arg225Trp) rs371723224
NM_004082.4(DCTN1):c.694G>C (p.Glu232Gln)
NM_004082.4(DCTN1):c.742C>G (p.Leu248Val)
NM_004082.4(DCTN1):c.821G>A (p.Arg274Gln)
NM_004082.4(DCTN1):c.823C>T (p.Arg275Cys) rs775294408
NM_004082.4(DCTN1):c.824G>A (p.Arg275His) rs375266113
NM_004082.4(DCTN1):c.833A>T (p.Glu278Val) rs1553465344
NM_004082.4(DCTN1):c.843+5G>T rs757238618
NM_004082.4(DCTN1):c.851A>G (p.Lys284Arg)

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