ClinVar Miner

List of variants in gene DYNC1H1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 96
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HGVS dbSNP gnomAD frequency
NM_001376.5(DYNC1H1):c.7410G>A (p.Ala2470=) rs139109090 0.00548
NM_001376.5(DYNC1H1):c.10293C>T (p.Asn3431=) rs75075497 0.00332
NM_001376.5(DYNC1H1):c.1587C>T (p.Asn529=) rs138418906 0.00302
NM_001376.5(DYNC1H1):c.5298G>T (p.Leu1766=) rs149395439 0.00286
NM_001376.5(DYNC1H1):c.7239G>T (p.Leu2413=) rs138407720 0.00175
NM_001376.5(DYNC1H1):c.5001C>T (p.Asn1667=) rs117199211 0.00137
NM_001376.5(DYNC1H1):c.8304G>A (p.Pro2768=) rs77113510 0.00132
NM_001376.5(DYNC1H1):c.13764G>A (p.Thr4588=) rs35079638 0.00088
NM_001376.5(DYNC1H1):c.10065T>C (p.Ser3355=) rs80096622 0.00087
NM_001376.5(DYNC1H1):c.2719-6C>T rs199763298 0.00078
NM_001376.5(DYNC1H1):c.5985C>T (p.Ala1995=) rs140841480 0.00059
NM_001376.5(DYNC1H1):c.10440G>A (p.Lys3480=) rs138887857 0.00056
NM_001376.5(DYNC1H1):c.8784A>G (p.Gln2928=) rs149753029 0.00056
NM_001376.5(DYNC1H1):c.10908+10G>A rs201277756 0.00045
NM_001376.5(DYNC1H1):c.7203A>C (p.Lys2401Asn) rs150888094 0.00032
NM_001376.5(DYNC1H1):c.5971G>A (p.Asp1991Asn) rs151001016 0.00030
NM_001376.5(DYNC1H1):c.7192C>T (p.Arg2398Cys) rs141525226 0.00030
NM_001376.5(DYNC1H1):c.1704T>C (p.Leu568=) rs192959810 0.00021
NM_001376.5(DYNC1H1):c.13808G>T (p.Ser4603Ile) rs200731839 0.00020
NM_001376.5(DYNC1H1):c.4176T>C (p.Gly1392=) rs112261870 0.00020
NM_001376.5(DYNC1H1):c.10522C>A (p.Leu3508Ile) rs149496322 0.00019
NM_001376.5(DYNC1H1):c.13683G>A (p.Thr4561=) rs192742245 0.00017
NM_001376.5(DYNC1H1):c.2025T>C (p.Asn675=) rs140154194 0.00017
NM_001376.5(DYNC1H1):c.369C>T (p.Pro123=) rs372944247 0.00016
NM_001376.5(DYNC1H1):c.8478A>G (p.Ala2826=) rs117846737 0.00016
NM_001376.5(DYNC1H1):c.8502A>G (p.Gln2834=) rs146220233 0.00016
NM_001376.5(DYNC1H1):c.12102+6G>A rs377669980 0.00014
NM_001376.5(DYNC1H1):c.12075C>T (p.Leu4025=) rs373636519 0.00013
NM_001376.5(DYNC1H1):c.13349C>T (p.Thr4450Met) rs146087540 0.00013
NM_001376.5(DYNC1H1):c.10887C>T (p.Phe3629=) rs141133453 0.00012
NM_001376.5(DYNC1H1):c.12939C>T (p.Pro4313=) rs151172467 0.00011
NM_001376.5(DYNC1H1):c.13113C>T (p.Asp4371=) rs372518648 0.00011
NM_001376.5(DYNC1H1):c.2211T>A (p.Val737=) rs149902566 0.00010
NM_001376.5(DYNC1H1):c.7317C>T (p.His2439=) rs200197781 0.00010
NM_001376.5(DYNC1H1):c.7758C>T (p.Ala2586=) rs145487328 0.00010
NM_001376.5(DYNC1H1):c.13404G>A (p.Thr4468=) rs17541692 0.00008
NM_001376.5(DYNC1H1):c.6795C>T (p.Tyr2265=) rs200339812 0.00008
NM_001376.5(DYNC1H1):c.8199C>T (p.Val2733=) rs770775119 0.00008
NM_001376.5(DYNC1H1):c.12031A>G (p.Thr4011Ala) rs753650013 0.00006
NM_001376.5(DYNC1H1):c.10203C>T (p.Asn3401=) rs369455947 0.00005
NM_001376.5(DYNC1H1):c.12345C>T (p.Ser4115=) rs774128776 0.00005
NM_001376.5(DYNC1H1):c.5326G>A (p.Ala1776Thr) rs200722698 0.00005
NM_001376.5(DYNC1H1):c.5874C>T (p.Asp1958=) rs142726284 0.00005
NM_001376.5(DYNC1H1):c.10941G>A (p.Pro3647=) rs374214760 0.00004
NM_001376.5(DYNC1H1):c.11873G>T (p.Gly3958Val) rs150118849 0.00004
NM_001376.5(DYNC1H1):c.4484A>G (p.Asn1495Ser) rs566164007 0.00004
NM_001376.5(DYNC1H1):c.5970C>T (p.Tyr1990=) rs751526144 0.00004
NM_001376.5(DYNC1H1):c.6909C>T (p.Phe2303=) rs138326082 0.00004
NM_001376.5(DYNC1H1):c.11460+4G>A rs201518717 0.00003
NM_001376.5(DYNC1H1):c.1296A>G (p.Val432=) rs767564445 0.00003
NM_001376.5(DYNC1H1):c.13651G>A (p.Ala4551Thr) rs145366078 0.00003
NM_001376.5(DYNC1H1):c.6904G>A (p.Val2302Ile) rs561339487 0.00003
NM_001376.5(DYNC1H1):c.7308G>A (p.Ala2436=) rs754446530 0.00003
NM_001376.5(DYNC1H1):c.8292G>A (p.Thr2764=) rs376429387 0.00003
NM_001376.5(DYNC1H1):c.8427G>A (p.Ala2809=) rs534435923 0.00003
NM_001376.5(DYNC1H1):c.10833G>C (p.Arg3611=) rs35143882 0.00002
NM_001376.5(DYNC1H1):c.12480G>A (p.Thr4160=) rs531519870 0.00002
NM_001376.5(DYNC1H1):c.12951G>A (p.Thr4317=) rs141273501 0.00002
NM_001376.5(DYNC1H1):c.13242G>A (p.Glu4414=) rs772150327 0.00002
NM_001376.5(DYNC1H1):c.13314C>T (p.Cys4438=) rs750291750 0.00002
NM_001376.5(DYNC1H1):c.3765C>T (p.Thr1255=) rs150953878 0.00002
NM_001376.5(DYNC1H1):c.5424A>G (p.Leu1808=) rs770425304 0.00002
NM_001376.5(DYNC1H1):c.7113C>T (p.Thr2371=) rs745348478 0.00002
NM_001376.5(DYNC1H1):c.7437C>T (p.Phe2479=) rs757950114 0.00002
NM_001376.5(DYNC1H1):c.10356C>T (p.Ala3452=) rs758827732 0.00001
NM_001376.5(DYNC1H1):c.12879C>T (p.Asp4293=) rs772763192 0.00001
NM_001376.5(DYNC1H1):c.1542T>C (p.Ala514=) rs1178479635 0.00001
NM_001376.5(DYNC1H1):c.2487T>C (p.Leu829=) rs1222196177 0.00001
NM_001376.5(DYNC1H1):c.4215C>T (p.Ser1405=) rs748713162 0.00001
NM_001376.5(DYNC1H1):c.432G>A (p.Ser144=) rs533327200 0.00001
NM_001376.5(DYNC1H1):c.4419T>C (p.Tyr1473=) rs747519168 0.00001
NM_001376.5(DYNC1H1):c.4542+6G>A rs375822798 0.00001
NM_001376.5(DYNC1H1):c.5327C>T (p.Ala1776Val) rs201902137 0.00001
NM_001376.5(DYNC1H1):c.5907G>A (p.Ser1969=) rs758999145 0.00001
NM_001376.5(DYNC1H1):c.8344-4A>G rs200913985 0.00001
NM_001376.5(DYNC1H1):c.10713C>T (p.Asp3571=) rs1177988460
NM_001376.5(DYNC1H1):c.11511C>T (p.His3837=)
NM_001376.5(DYNC1H1):c.12564G>A (p.Ala4188=) rs370064490
NM_001376.5(DYNC1H1):c.13203C>T (p.Thr4401=) rs138022242
NM_001376.5(DYNC1H1):c.13812+63C>T
NM_001376.5(DYNC1H1):c.150C>G (p.Ala50=) rs372404851
NM_001376.5(DYNC1H1):c.2085G>A (p.Thr695=) rs755760078
NM_001376.5(DYNC1H1):c.2085G>T (p.Thr695=)
NM_001376.5(DYNC1H1):c.4203T>C (p.Ile1401=)
NM_001376.5(DYNC1H1):c.5004G>A (p.Glu1668=)
NM_001376.5(DYNC1H1):c.5046G>A (p.Glu1682=)
NM_001376.5(DYNC1H1):c.5209A>G (p.Thr1737Ala) rs1064797192
NM_001376.5(DYNC1H1):c.5811T>C (p.Asp1937=)
NM_001376.5(DYNC1H1):c.6348G>A (p.Glu2116=)
NM_001376.5(DYNC1H1):c.6406-4G>A rs374602014
NM_001376.5(DYNC1H1):c.6759C>T (p.Ile2253=) rs1595615114
NM_001376.5(DYNC1H1):c.6871G>A (p.Val2291Met)
NM_001376.5(DYNC1H1):c.7146G>A (p.Leu2382=) rs2152581549
NM_001376.5(DYNC1H1):c.7863C>T (p.Asn2621=)
NM_001376.5(DYNC1H1):c.8214C>T (p.Tyr2738=)
NM_001376.5(DYNC1H1):c.8280A>C (p.Pro2760=)

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