ClinVar Miner

List of variants in gene combination DYNC1H1, LOC126862060 reported by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 48
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001376.5(DYNC1H1):c.9468+108T>C rs4906173 0.34566
NM_001376.5(DYNC1H1):c.8928A>G (p.Leu2976=) rs8010870 0.14754
NM_001376.5(DYNC1H1):c.9138G>T (p.Ser3046=) rs34338935 0.00261
NM_001376.5(DYNC1H1):c.9264-8T>G rs368432468 0.00123
NM_001376.5(DYNC1H1):c.9264-29C>G rs17512607 0.00093
NM_001376.5(DYNC1H1):c.9049-36G>A rs118014540 0.00080
NM_001376.5(DYNC1H1):c.9048+31G>A rs186161486 0.00061
NM_001376.5(DYNC1H1):c.9468+43C>T rs147162427 0.00061
NM_001376.5(DYNC1H1):c.9171G>A (p.Gln3057=) rs201041097 0.00023
NM_001376.5(DYNC1H1):c.9093G>A (p.Thr3031=) rs145208135 0.00019
NM_001376.5(DYNC1H1):c.9324A>G (p.Glu3108=) rs142338762 0.00011
NM_001376.5(DYNC1H1):c.9263+38C>T rs370223723 0.00010
NM_001376.5(DYNC1H1):c.9402G>A (p.Pro3134=) rs145095254 0.00006
NM_001376.5(DYNC1H1):c.9049-19G>T rs369055747 0.00003
NM_001376.5(DYNC1H1):c.9189C>T (p.His3063=) rs373124911 0.00003
NM_001376.5(DYNC1H1):c.9075G>A (p.Glu3025=) rs777623931 0.00002
NM_001376.5(DYNC1H1):c.9178C>T (p.Arg3060Cys) rs773658296 0.00002
NM_001376.5(DYNC1H1):c.9263+4C>T rs375319205 0.00002
NM_001376.5(DYNC1H1):c.8887-13T>G rs766982598 0.00001
NM_001376.5(DYNC1H1):c.8954G>C (p.Cys2985Ser) rs1269870036 0.00001
NM_001376.5(DYNC1H1):c.9049G>A (p.Val3017Met) rs879254170 0.00001
NM_001376.5(DYNC1H1):c.9077A>G (p.Tyr3026Cys) rs1032073396 0.00001
NM_001376.5(DYNC1H1):c.9210G>A (p.Pro3070=) rs201817995 0.00001
NM_001376.5(DYNC1H1):c.9232C>T (p.Arg3078Trp) rs2503805342 0.00001
NM_001376.5(DYNC1H1):c.9249A>G (p.Pro3083=) rs1555410963 0.00001
NM_001376.5(DYNC1H1):c.8929C>T (p.Arg2977Trp) rs2503804194
NM_001376.5(DYNC1H1):c.8945G>T (p.Arg2982Leu) rs2048463341
NM_001376.5(DYNC1H1):c.8972C>T (p.Ala2991Val) rs2503804353
NM_001376.5(DYNC1H1):c.9049-5C>T rs1555410928
NM_001376.5(DYNC1H1):c.9057T>A (p.Gly3019=) rs778613903
NM_001376.5(DYNC1H1):c.9069A>G (p.Gly3023=) rs532073330
NM_001376.5(DYNC1H1):c.9092C>T (p.Thr3031Met) rs879253956
NM_001376.5(DYNC1H1):c.9109del (p.Ala3037fs)
NM_001376.5(DYNC1H1):c.9127A>G (p.Met3043Val)
NM_001376.5(DYNC1H1):c.9142G>A (p.Glu3048Lys) rs1555410941
NM_001376.5(DYNC1H1):c.9182A>G (p.Asn3061Ser) rs2503805212
NM_001376.5(DYNC1H1):c.9242C>T (p.Thr3081Ile) rs1555410958
NM_001376.5(DYNC1H1):c.9265T>C (p.Cys3089Arg)
NM_001376.5(DYNC1H1):c.9275A>G (p.Asn3092Ser) rs2503805771
NM_001376.5(DYNC1H1):c.9280T>C (p.Phe3094Leu) rs2152589291
NM_001376.5(DYNC1H1):c.9320A>G (p.Lys3107Arg)
NM_001376.5(DYNC1H1):c.9333T>A (p.Ser3111Arg) rs879254260
NM_001376.5(DYNC1H1):c.9335A>G (p.Lys3112Arg) rs374952401
NM_001376.5(DYNC1H1):c.9363C>G (p.Ile3121Met) rs547968657
NM_001376.5(DYNC1H1):c.9371A>C (p.Asp3124Ala) rs2152589337
NM_001376.5(DYNC1H1):c.9402G>T (p.Pro3134=) rs145095254
NM_001376.5(DYNC1H1):c.9449T>G (p.Val3150Gly) rs2152589394
NM_001376.5(DYNC1H1):c.9463C>T (p.His3155Tyr) rs2503806489

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.