ClinVar Miner

List of variants in gene DYNC1H1 reported as uncertain significance by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 221
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001376.5(DYNC1H1):c.11366T>C (p.Ile3789Thr) rs775444653 0.00015
NM_001376.5(DYNC1H1):c.8584G>A (p.Asp2862Asn) rs139461837 0.00013
NM_001376.5(DYNC1H1):c.-3A>G rs369550020 0.00010
NM_001376.5(DYNC1H1):c.3334-4T>C rs368422942 0.00007
NM_001376.5(DYNC1H1):c.13072G>A (p.Ala4358Thr) rs547205132 0.00006
NM_001376.5(DYNC1H1):c.623C>T (p.Pro208Leu) rs556010695 0.00006
NM_001376.5(DYNC1H1):c.10292A>G (p.Asn3431Ser) rs764127291 0.00005
NM_001376.5(DYNC1H1):c.6029C>T (p.Pro2010Leu) rs747348966 0.00005
NM_001376.5(DYNC1H1):c.13303G>A (p.Val4435Ile) rs767195767 0.00004
NM_001376.5(DYNC1H1):c.2869-3C>T rs750614475 0.00004
NM_001376.5(DYNC1H1):c.3571C>T (p.Arg1191Cys) rs774198261 0.00004
NM_001376.5(DYNC1H1):c.6857+5G>A rs371934648 0.00004
NM_001376.5(DYNC1H1):c.7116C>A (p.Asp2372Glu) rs377242217 0.00004
NM_001376.5(DYNC1H1):c.7193G>A (p.Arg2398His) rs912429154 0.00004
NM_001376.5(DYNC1H1):c.12496G>A (p.Val4166Ile) rs202107738 0.00003
NM_001376.5(DYNC1H1):c.12788G>A (p.Arg4263His) rs762441496 0.00003
NM_001376.5(DYNC1H1):c.13651G>A (p.Ala4551Thr) rs145366078 0.00003
NM_001376.5(DYNC1H1):c.161C>T (p.Ala54Val) rs772070566 0.00003
NM_001376.5(DYNC1H1):c.2768C>T (p.Thr923Met) rs760518511 0.00003
NM_001376.5(DYNC1H1):c.5197A>G (p.Ile1733Val) rs138287354 0.00003
NM_001376.5(DYNC1H1):c.851C>T (p.Ala284Val) rs774677904 0.00003
NM_001376.5(DYNC1H1):c.12797A>G (p.Asn4266Ser) rs760229878 0.00002
NM_001376.5(DYNC1H1):c.2374T>G (p.Cys792Gly) rs752495590 0.00002
NM_001376.5(DYNC1H1):c.4075-5G>A rs750127672 0.00002
NM_001376.5(DYNC1H1):c.4597C>G (p.Leu1533Val) rs775825001 0.00002
NM_001376.5(DYNC1H1):c.6704G>A (p.Arg2235His) rs765956720 0.00002
NM_001376.5(DYNC1H1):c.7225G>A (p.Ala2409Thr) rs566204008 0.00002
NM_001376.5(DYNC1H1):c.8442G>C (p.Glu2814Asp) rs762494017 0.00002
NM_001376.5(DYNC1H1):c.9797A>T (p.Lys3266Met) rs765825369 0.00002
NM_001376.5(DYNC1H1):c.10241A>G (p.Asn3414Ser) rs1555411393 0.00001
NM_001376.5(DYNC1H1):c.10743A>C (p.Lys3581Asn) rs768668529 0.00001
NM_001376.5(DYNC1H1):c.10832G>A (p.Arg3611Gln) rs760957660 0.00001
NM_001376.5(DYNC1H1):c.10970G>C (p.Gly3657Ala) rs761427653 0.00001
NM_001376.5(DYNC1H1):c.11795C>T (p.Ala3932Val) rs752716582 0.00001
NM_001376.5(DYNC1H1):c.11897C>T (p.Pro3966Leu) rs879254021 0.00001
NM_001376.5(DYNC1H1):c.12112A>C (p.Asn4038His) rs1271427633 0.00001
NM_001376.5(DYNC1H1):c.12115A>G (p.Thr4039Ala) rs774809334 0.00001
NM_001376.5(DYNC1H1):c.1260T>G (p.Phe420Leu) rs1367292809 0.00001
NM_001376.5(DYNC1H1):c.13204G>A (p.Val4402Met) rs977186240 0.00001
NM_001376.5(DYNC1H1):c.13297G>A (p.Asp4433Asn) rs749297332 0.00001
NM_001376.5(DYNC1H1):c.13408C>T (p.Pro4470Ser) rs150906249 0.00001
NM_001376.5(DYNC1H1):c.1360C>T (p.Pro454Ser) rs1362114769 0.00001
NM_001376.5(DYNC1H1):c.13652C>T (p.Ala4551Val) rs1181756021 0.00001
NM_001376.5(DYNC1H1):c.13682C>T (p.Thr4561Met) rs1376784009 0.00001
NM_001376.5(DYNC1H1):c.13750G>A (p.Ala4584Thr) rs544608488 0.00001
NM_001376.5(DYNC1H1):c.13771C>T (p.Arg4591Cys) rs765362140 0.00001
NM_001376.5(DYNC1H1):c.2294T>C (p.Val765Ala) rs1001125376 0.00001
NM_001376.5(DYNC1H1):c.2369G>A (p.Arg790Gln) rs371431746 0.00001
NM_001376.5(DYNC1H1):c.2393G>A (p.Arg798Gln) rs768932305 0.00001
NM_001376.5(DYNC1H1):c.2504G>A (p.Arg835His) rs1463717963 0.00001
NM_001376.5(DYNC1H1):c.2584C>T (p.Arg862Cys) rs865971340 0.00001
NM_001376.5(DYNC1H1):c.265G>A (p.Gly89Ser) rs749973847 0.00001
NM_001376.5(DYNC1H1):c.3015+3A>G rs1057522534 0.00001
NM_001376.5(DYNC1H1):c.3444+3G>A rs1475876803 0.00001
NM_001376.5(DYNC1H1):c.3572G>A (p.Arg1191His) rs1003718521 0.00001
NM_001376.5(DYNC1H1):c.3583C>T (p.Arg1195Cys) rs767427937 0.00001
NM_001376.5(DYNC1H1):c.370G>A (p.Val124Met) rs749548033 0.00001
NM_001376.5(DYNC1H1):c.3955G>A (p.Val1319Met) rs370976687 0.00001
NM_001376.5(DYNC1H1):c.4264G>A (p.Val1422Ile) rs760230019 0.00001
NM_001376.5(DYNC1H1):c.4543-5A>C rs903101532 0.00001
NM_001376.5(DYNC1H1):c.4657G>A (p.Gly1553Ser) rs767868450 0.00001
NM_001376.5(DYNC1H1):c.4851A>C (p.Glu1617Asp) rs1060502204 0.00001
NM_001376.5(DYNC1H1):c.6502G>A (p.Val2168Ile) rs1567010429 0.00001
NM_001376.5(DYNC1H1):c.6857+4C>T rs374773368 0.00001
NM_001376.5(DYNC1H1):c.7262C>T (p.Thr2421Met) rs770803375 0.00001
NM_001376.5(DYNC1H1):c.8876A>G (p.Tyr2959Cys) rs797045536 0.00001
NM_001376.5(DYNC1H1):c.92A>G (p.Gln31Arg) rs1043956265 0.00001
NM_001376.5(DYNC1H1):c.994T>C (p.Tyr332His) rs764842673 0.00001
NM_001376.5(DYNC1H1):c.10267G>A (p.Ala3423Thr)
NM_001376.5(DYNC1H1):c.1026T>G (p.Asn342Lys)
NM_001376.5(DYNC1H1):c.10473A>C (p.Lys3491Asn)
NM_001376.5(DYNC1H1):c.10549G>A (p.Ala3517Thr) rs2152592178
NM_001376.5(DYNC1H1):c.10640T>G (p.Ile3547Ser)
NM_001376.5(DYNC1H1):c.1072_1078dup (p.Ile360fs)
NM_001376.5(DYNC1H1):c.10738C>G (p.Leu3580Val)
NM_001376.5(DYNC1H1):c.107A>G (p.Lys36Arg)
NM_001376.5(DYNC1H1):c.10933T>A (p.Leu3645Met)
NM_001376.5(DYNC1H1):c.1117C>A (p.Pro373Thr)
NM_001376.5(DYNC1H1):c.11221C>T (p.Arg3741Cys) rs2048610848
NM_001376.5(DYNC1H1):c.11543G>A (p.Gly3848Asp) rs754712755
NM_001376.5(DYNC1H1):c.11630A>C (p.His3877Pro)
NM_001376.5(DYNC1H1):c.11683A>T (p.Thr3895Ser)
NM_001376.5(DYNC1H1):c.11806G>T (p.Val3936Leu) rs780676515
NM_001376.5(DYNC1H1):c.11858C>T (p.Ala3953Val)
NM_001376.5(DYNC1H1):c.11915_11917dup (p.Tyr3972_Leu3973insHis)
NM_001376.5(DYNC1H1):c.11933C>T (p.Thr3978Ile)
NM_001376.5(DYNC1H1):c.11950G>C (p.Gly3984Arg)
NM_001376.5(DYNC1H1):c.11989C>T (p.Arg3997Trp) rs1399236395
NM_001376.5(DYNC1H1):c.11990G>A (p.Arg3997Gln)
NM_001376.5(DYNC1H1):c.12076G>A (p.Asp4026Asn)
NM_001376.5(DYNC1H1):c.12211A>G (p.Ile4071Val) rs797044851
NM_001376.5(DYNC1H1):c.12215-4C>T rs1174367006
NM_001376.5(DYNC1H1):c.12247G>T (p.Ala4083Ser)
NM_001376.5(DYNC1H1):c.12269C>T (p.Ser4090Leu)
NM_001376.5(DYNC1H1):c.12457G>T (p.Val4153Leu) rs2048667081
NM_001376.5(DYNC1H1):c.12494C>T (p.Pro4165Leu) rs1567022806
NM_001376.5(DYNC1H1):c.12677C>A (p.Thr4226Lys)
NM_001376.5(DYNC1H1):c.12869G>A (p.Gly4290Glu) rs1555412242
NM_001376.5(DYNC1H1):c.12982G>A (p.Glu4328Lys)
NM_001376.5(DYNC1H1):c.13042A>C (p.Met4348Leu) rs879254327
NM_001376.5(DYNC1H1):c.13060G>T (p.Asp4354Tyr) rs1449580462
NM_001376.5(DYNC1H1):c.13106C>T (p.Thr4369Met) rs1290022379
NM_001376.5(DYNC1H1):c.13132C>T (p.Arg4378Trp)
NM_001376.5(DYNC1H1):c.13166A>G (p.His4389Arg) rs1206639344
NM_001376.5(DYNC1H1):c.1318A>G (p.Arg440Gly) rs1566997890
NM_001376.5(DYNC1H1):c.13265A>C (p.Lys4422Thr) rs1463058227
NM_001376.5(DYNC1H1):c.13294G>A (p.Ala4432Thr) rs1567025587
NM_001376.5(DYNC1H1):c.13384C>T (p.Arg4462Trp) rs879253914
NM_001376.5(DYNC1H1):c.13484C>G (p.Ala4495Gly)
NM_001376.5(DYNC1H1):c.13710CAA[3] (p.Asn4573del) rs1013209915
NM_001376.5(DYNC1H1):c.13730T>C (p.Leu4577Pro) rs1567026417
NM_001376.5(DYNC1H1):c.13747A>G (p.Thr4583Ala)
NM_001376.5(DYNC1H1):c.13775G>C (p.Trp4592Ser)
NM_001376.5(DYNC1H1):c.13777G>A (p.Val4593Ile) rs750566844
NM_001376.5(DYNC1H1):c.13784A>G (p.Gln4595Arg) rs2048787955
NM_001376.5(DYNC1H1):c.13785_13788del (p.Asn4597fs) rs2048787913
NM_001376.5(DYNC1H1):c.13844G>A (p.Arg4615His)
NM_001376.5(DYNC1H1):c.1384C>T (p.Arg462Cys)
NM_001376.5(DYNC1H1):c.13864G>A (p.Val4622Met)
NM_001376.5(DYNC1H1):c.1462-3T>C
NM_001376.5(DYNC1H1):c.1477C>A (p.Gln493Lys) rs1298953581
NM_001376.5(DYNC1H1):c.1688G>A (p.Arg563Gln)
NM_001376.5(DYNC1H1):c.1748G>A (p.Arg583Lys) rs2047932366
NM_001376.5(DYNC1H1):c.182C>T (p.Ala61Val)
NM_001376.5(DYNC1H1):c.2081A>T (p.Asn694Ile)
NM_001376.5(DYNC1H1):c.2102A>C (p.Asp701Ala)
NM_001376.5(DYNC1H1):c.2156C>T (p.Thr719Ile) rs775702816
NM_001376.5(DYNC1H1):c.223C>T (p.His75Tyr)
NM_001376.5(DYNC1H1):c.2288C>T (p.Ala763Val) rs1358924141
NM_001376.5(DYNC1H1):c.2357G>A (p.Arg786His)
NM_001376.5(DYNC1H1):c.2401A>G (p.Ile801Val)
NM_001376.5(DYNC1H1):c.2536A>G (p.Lys846Glu)
NM_001376.5(DYNC1H1):c.2678A>G (p.Tyr893Cys) rs2141275840
NM_001376.5(DYNC1H1):c.277GAA[2] (p.Glu95del) rs913021962
NM_001376.5(DYNC1H1):c.2807T>G (p.Val936Gly)
NM_001376.5(DYNC1H1):c.2833G>A (p.Val945Ile) rs2141276701
NM_001376.5(DYNC1H1):c.2851G>A (p.Gly951Arg) rs2141276704
NM_001376.5(DYNC1H1):c.2861A>G (p.Lys954Arg)
NM_001376.5(DYNC1H1):c.2999A>G (p.Gln1000Arg)
NM_001376.5(DYNC1H1):c.3016-5G>T
NM_001376.5(DYNC1H1):c.3016-6G>A
NM_001376.5(DYNC1H1):c.3026A>G (p.His1009Arg)
NM_001376.5(DYNC1H1):c.3063T>A (p.Asn1021Lys)
NM_001376.5(DYNC1H1):c.3088C>T (p.Pro1030Ser)
NM_001376.5(DYNC1H1):c.3184G>A (p.Asp1062Asn) rs2048038347
NM_001376.5(DYNC1H1):c.319A>G (p.Ile107Val)
NM_001376.5(DYNC1H1):c.3680G>A (p.Arg1227Gln) rs2048071941
NM_001376.5(DYNC1H1):c.3734A>G (p.Gln1245Arg) rs2141282700
NM_001376.5(DYNC1H1):c.3758G>A (p.Arg1253His)
NM_001376.5(DYNC1H1):c.4054G>A (p.Val1352Ile)
NM_001376.5(DYNC1H1):c.4074+5A>G rs1567005739
NM_001376.5(DYNC1H1):c.4140T>G (p.Tyr1380Ter) rs1567006190
NM_001376.5(DYNC1H1):c.4231C>T (p.Arg1411Cys) rs1567006266
NM_001376.5(DYNC1H1):c.4289C>A (p.Thr1430Asn) rs1171366952
NM_001376.5(DYNC1H1):c.4572A>T (p.Glu1524Asp) rs2048144507
NM_001376.5(DYNC1H1):c.4768G>C (p.Asp1590His) rs200700087
NM_001376.5(DYNC1H1):c.47T>C (p.Leu16Ser)
NM_001376.5(DYNC1H1):c.4841C>T (p.Ala1614Val)
NM_001376.5(DYNC1H1):c.4937A>G (p.Asn1646Ser) rs2141288481
NM_001376.5(DYNC1H1):c.5121G>C (p.Lys1707Asn)
NM_001376.5(DYNC1H1):c.5176A>G (p.Ile1726Val)
NM_001376.5(DYNC1H1):c.5215A>G (p.Ile1739Val)
NM_001376.5(DYNC1H1):c.5240C>G (p.Ala1747Gly)
NM_001376.5(DYNC1H1):c.53T>C (p.Val18Ala)
NM_001376.5(DYNC1H1):c.5405C>T (p.Pro1802Leu)
NM_001376.5(DYNC1H1):c.5459A>G (p.Asp1820Gly)
NM_001376.5(DYNC1H1):c.5471C>T (p.Ser1824Phe)
NM_001376.5(DYNC1H1):c.568G>A (p.Glu190Lys) rs1566996419
NM_001376.5(DYNC1H1):c.5773C>T (p.Arg1925Trp)
NM_001376.5(DYNC1H1):c.580C>G (p.Leu194Val)
NM_001376.5(DYNC1H1):c.5875G>A (p.Glu1959Lys)
NM_001376.5(DYNC1H1):c.6101A>G (p.Lys2034Arg)
NM_001376.5(DYNC1H1):c.6278T>C (p.Leu2093Ser)
NM_001376.5(DYNC1H1):c.6353G>A (p.Arg2118Gln) rs1060502207
NM_001376.5(DYNC1H1):c.6485C>T (p.Ser2162Leu)
NM_001376.5(DYNC1H1):c.6511C>T (p.His2171Tyr) rs1060502208
NM_001376.5(DYNC1H1):c.6595_6596del (p.Val2199fs)
NM_001376.5(DYNC1H1):c.6606G>C (p.Met2202Ile)
NM_001376.5(DYNC1H1):c.6618+5C>T rs777017923
NM_001376.5(DYNC1H1):c.6718G>T (p.Ala2240Ser)
NM_001376.5(DYNC1H1):c.6736G>A (p.Gly2246Ser)
NM_001376.5(DYNC1H1):c.6767C>A (p.Pro2256His)
NM_001376.5(DYNC1H1):c.685G>A (p.Val229Ile)
NM_001376.5(DYNC1H1):c.6871G>A (p.Val2291Met)
NM_001376.5(DYNC1H1):c.7072C>T (p.Arg2358Cys) rs879254019
NM_001376.5(DYNC1H1):c.7174G>A (p.Asp2392Asn)
NM_001376.5(DYNC1H1):c.7214G>T (p.Gly2405Val)
NM_001376.5(DYNC1H1):c.7400G>T (p.Arg2467Leu)
NM_001376.5(DYNC1H1):c.7439C>T (p.Pro2480Leu) rs1229845145
NM_001376.5(DYNC1H1):c.7450G>T (p.Glu2484Ter)
NM_001376.5(DYNC1H1):c.752G>A (p.Arg251His) rs794727634
NM_001376.5(DYNC1H1):c.7549T>C (p.Tyr2517His) rs1567012503
NM_001376.5(DYNC1H1):c.7561A>G (p.Ile2521Val)
NM_001376.5(DYNC1H1):c.7615-4G>A
NM_001376.5(DYNC1H1):c.7625G>A (p.Ser2542Asn)
NM_001376.5(DYNC1H1):c.7625G>C (p.Ser2542Thr)
NM_001376.5(DYNC1H1):c.7679A>G (p.His2560Arg) rs1567012734
NM_001376.5(DYNC1H1):c.7729C>T (p.His2577Tyr)
NM_001376.5(DYNC1H1):c.7732G>A (p.Glu2578Lys) rs749628606
NM_001376.5(DYNC1H1):c.8056A>T (p.Met2686Leu)
NM_001376.5(DYNC1H1):c.8081G>A (p.Arg2694His)
NM_001376.5(DYNC1H1):c.816A>C (p.Leu272Phe) rs1555407950
NM_001376.5(DYNC1H1):c.8287C>T (p.Arg2763Trp)
NM_001376.5(DYNC1H1):c.829T>G (p.Phe277Val) rs1057518935
NM_001376.5(DYNC1H1):c.8339C>G (p.Ser2780Cys)
NM_001376.5(DYNC1H1):c.8444C>T (p.Thr2815Ile)
NM_001376.5(DYNC1H1):c.8461C>G (p.Leu2821Val) rs2048366964
NM_001376.5(DYNC1H1):c.8568G>T (p.Lys2856Asn)
NM_001376.5(DYNC1H1):c.8599A>G (p.Met2867Val)
NM_001376.5(DYNC1H1):c.8637_8638insTATA (p.Asp2880fs)
NM_001376.5(DYNC1H1):c.8650G>A (p.Val2884Ile)
NM_001376.5(DYNC1H1):c.874C>T (p.Arg292Trp) rs2047850664
NM_001376.5(DYNC1H1):c.889G>A (p.Val297Ile)
NM_001376.5(DYNC1H1):c.9496G>A (p.Gly3166Ser) rs1393341368
NM_001376.5(DYNC1H1):c.9554A>G (p.Asn3185Ser)
NM_001376.5(DYNC1H1):c.9579G>T (p.Glu3193Asp)
NM_001376.5(DYNC1H1):c.9607G>A (p.Val3203Met) rs1567017825
NM_001376.5(DYNC1H1):c.9691G>T (p.Val3231Leu) rs1567017900
NM_001376.5(DYNC1H1):c.9762+4T>C
NM_001376.5(DYNC1H1):c.9762+4T>G
NM_001376.5(DYNC1H1):c.9827T>G (p.Met3276Arg)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.