ClinVar Miner

List of variants in gene DYNC1H1 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 94
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HGVS dbSNP gnomAD frequency
NM_001376.5(DYNC1H1):c.8304G>A (p.Pro2768=) rs77113510 0.00132
NM_001376.5(DYNC1H1):c.10065T>C (p.Ser3355=) rs80096622 0.00087
NM_001376.5(DYNC1H1):c.5310C>T (p.Gly1770=) rs34013442 0.00078
NM_001376.5(DYNC1H1):c.12258C>T (p.Thr4086=) rs141242095 0.00059
NM_001376.5(DYNC1H1):c.5985C>T (p.Ala1995=) rs140841480 0.00059
NM_001376.5(DYNC1H1):c.5294C>T (p.Ala1765Val) rs150687712 0.00058
NM_001376.5(DYNC1H1):c.8784A>G (p.Gln2928=) rs149753029 0.00056
NM_001376.5(DYNC1H1):c.1173A>G (p.Gln391=) rs17540735 0.00049
NM_001376.5(DYNC1H1):c.4509C>T (p.Ser1503=) rs116089522 0.00046
NM_001376.5(DYNC1H1):c.6762C>T (p.Ile2254=) rs150603103 0.00046
NM_001376.5(DYNC1H1):c.13181C>T (p.Thr4394Met) rs149300055 0.00042
NM_001376.5(DYNC1H1):c.4296C>G (p.Gly1432=) rs150374820 0.00037
NM_001376.5(DYNC1H1):c.5718A>C (p.Gly1906=) rs139070737 0.00035
NM_001376.5(DYNC1H1):c.9762+9T>G rs376545350 0.00033
NM_001376.5(DYNC1H1):c.-13C>G rs537857759 0.00026
NM_001376.5(DYNC1H1):c.11862C>T (p.Asp3954=) rs140543419 0.00021
NM_001376.5(DYNC1H1):c.1704T>C (p.Leu568=) rs192959810 0.00021
NM_001376.5(DYNC1H1):c.4176T>C (p.Gly1392=) rs112261870 0.00020
NM_001376.5(DYNC1H1):c.261C>T (p.Asp87=) rs75113705 0.00019
NM_001376.5(DYNC1H1):c.885G>A (p.Pro295=) rs34287672 0.00019
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.10332C>T (p.Ile3444=) rs145087182 0.00014
NM_001376.5(DYNC1H1):c.1308C>T (p.Asp436=) rs147531912 0.00014
NM_001376.5(DYNC1H1):c.12075C>T (p.Leu4025=) rs373636519 0.00013
NM_001376.5(DYNC1H1):c.12333G>A (p.Lys4111=) rs373520665 0.00012
NM_001376.5(DYNC1H1):c.7071G>A (p.Ser2357=) rs375808105 0.00012
NM_001376.5(DYNC1H1):c.657G>A (p.Gln219=) rs374440380 0.00011
NM_001376.5(DYNC1H1):c.11139A>G (p.Leu3713=) rs143642514 0.00010
NM_001376.5(DYNC1H1):c.13557G>A (p.Ala4519=) rs35546990 0.00010
NM_001376.5(DYNC1H1):c.7758C>T (p.Ala2586=) rs145487328 0.00010
NM_001376.5(DYNC1H1):c.13515+8C>T rs200901713 0.00009
NM_001376.5(DYNC1H1):c.13515+9G>A rs374678076 0.00009
NM_001376.5(DYNC1H1):c.13782G>A (p.Lys4594=) rs147580834 0.00009
NM_001376.5(DYNC1H1):c.2283A>G (p.Pro761=) rs202008601 0.00007
NM_001376.5(DYNC1H1):c.2376C>T (p.Cys792=) rs35092963 0.00007
NM_001376.5(DYNC1H1):c.3804+9C>T rs377635872 0.00007
NM_001376.5(DYNC1H1):c.11295G>A (p.Thr3765=) rs372847973 0.00005
NM_001376.5(DYNC1H1):c.12345C>T (p.Ser4115=) rs774128776 0.00005
NM_001376.5(DYNC1H1):c.12588C>T (p.Tyr4196=) rs749876358 0.00005
NM_001376.5(DYNC1H1):c.13407G>A (p.Val4469=) rs1445271324 0.00005
NM_001376.5(DYNC1H1):c.4843T>C (p.Leu1615=) rs375058473 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.1911C>T (p.His637=) rs376398498 0.00004
NM_001376.5(DYNC1H1):c.3419C>T (p.Thr1140Met) rs587780331 0.00004
NM_001376.5(DYNC1H1):c.6909C>T (p.Phe2303=) rs138326082 0.00004
NM_001376.5(DYNC1H1):c.7431C>T (p.Pro2477=) rs375687099 0.00004
NM_001376.5(DYNC1H1):c.939C>T (p.Thr313=) rs572233805 0.00004
NM_001376.5(DYNC1H1):c.10401T>A (p.Ala3467=) rs184264124 0.00003
NM_001376.5(DYNC1H1):c.10548C>T (p.Tyr3516=) rs760532492 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.11461-3C>T rs776752310 0.00002
NM_001376.5(DYNC1H1):c.1545A>G (p.Ala515=) rs145784659 0.00002
NM_001376.5(DYNC1H1):c.3414C>T (p.Asn1138=) rs772761222 0.00002
NM_001376.5(DYNC1H1):c.6339G>A (p.Arg2113=) rs776544497 0.00002
NM_001376.5(DYNC1H1):c.11130C>T (p.Ser3710=) rs749713831 0.00001
NM_001376.5(DYNC1H1):c.12705G>A (p.Pro4235=) rs199792795 0.00001
NM_001376.5(DYNC1H1):c.13539C>G (p.Gly4513=) rs1165803933 0.00001
NM_001376.5(DYNC1H1):c.2754C>T (p.Gly918=) rs543139363 0.00001
NM_001376.5(DYNC1H1):c.4510G>A (p.Val1504Ile) rs761695197 0.00001
NM_001376.5(DYNC1H1):c.4543-5A>C rs903101532 0.00001
NM_001376.5(DYNC1H1):c.4752G>A (p.Lys1584=) rs1436095321 0.00001
NM_001376.5(DYNC1H1):c.4959C>T (p.His1653=) rs773425996 0.00001
NM_001376.5(DYNC1H1):c.6882G>A (p.Glu2294=) rs772596156 0.00001
NM_001376.5(DYNC1H1):c.8262C>T (p.Ala2754=) rs758178917 0.00001
NM_001376.5(DYNC1H1):c.8754C>T (p.His2918=) rs758989267 0.00001
NM_001376.5(DYNC1H1):c.11058C>T (p.Val3686=)
NM_001376.5(DYNC1H1):c.1110A>C (p.Thr370=)
NM_001376.5(DYNC1H1):c.11866-4A>G rs766735095
NM_001376.5(DYNC1H1):c.11942-20_11947dup rs745960214
NM_001376.5(DYNC1H1):c.12399+10T>G rs1033442950
NM_001376.5(DYNC1H1):c.12564G>A (p.Ala4188=) rs370064490
NM_001376.5(DYNC1H1):c.1761G>A (p.Arg587=)
NM_001376.5(DYNC1H1):c.1854T>C (p.Ser618=)
NM_001376.5(DYNC1H1):c.3090T>C (p.Pro1030=)
NM_001376.5(DYNC1H1):c.3642C>T (p.Ile1214=) rs778273904
NM_001376.5(DYNC1H1):c.36C>G (p.Gly12=) rs373527972
NM_001376.5(DYNC1H1):c.3819A>G (p.Pro1273=) rs996115621
NM_001376.5(DYNC1H1):c.4185+21G>A
NM_001376.5(DYNC1H1):c.4185+25A>C
NM_001376.5(DYNC1H1):c.4911G>A (p.Leu1637=)
NM_001376.5(DYNC1H1):c.5079T>C (p.Thr1693=)
NM_001376.5(DYNC1H1):c.5343G>T (p.Val1781=)
NM_001376.5(DYNC1H1):c.6222-9_6222-7del rs747347010
NM_001376.5(DYNC1H1):c.6420C>T (p.Ser2140=)
NM_001376.5(DYNC1H1):c.7218G>A (p.Glu2406=)
NM_001376.5(DYNC1H1):c.7227T>C (p.Ala2409=)
NM_001376.5(DYNC1H1):c.7758C>G (p.Ala2586=) rs145487328
NM_001376.5(DYNC1H1):c.819G>A (p.Gln273=)
NM_001376.5(DYNC1H1):c.8508-8C>G
NM_001376.5(DYNC1H1):c.8574C>T (p.Phe2858=)

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