ClinVar Miner

List of variants in gene DYNC1H1 reported as uncertain significance for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 60
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001376.5(DYNC1H1):c.13440C>T (p.Ser4480=) rs150286673 0.00103
NM_001376.5(DYNC1H1):c.4515G>A (p.Ser1505=) rs186932188 0.00016
NM_001376.5(DYNC1H1):c.8502A>G (p.Gln2834=) rs146220233 0.00016
NM_001376.5(DYNC1H1):c.3156+5G>A rs200905961 0.00015
NM_001376.5(DYNC1H1):c.7758C>T (p.Ala2586=) rs145487328 0.00010
NM_001376.5(DYNC1H1):c.5655T>A (p.Thr1885=) rs538791873 0.00009
NM_001376.5(DYNC1H1):c.11520A>G (p.Leu3840=) rs369351359 0.00006
NM_001376.5(DYNC1H1):c.13072G>A (p.Ala4358Thr) rs547205132 0.00006
NM_001376.5(DYNC1H1):c.2737G>A (p.Val913Ile) rs372740994 0.00005
NM_001376.5(DYNC1H1):c.4484A>G (p.Asn1495Ser) rs566164007 0.00004
NM_001376.5(DYNC1H1):c.8637+9C>T rs202042156 0.00004
NM_001376.5(DYNC1H1):c.10548C>T (p.Tyr3516=) rs760532492 0.00003
NM_001376.5(DYNC1H1):c.11460+4G>A rs201518717 0.00003
NM_001376.5(DYNC1H1):c.13261G>A (p.Ala4421Thr) rs376492799 0.00003
NM_001376.5(DYNC1H1):c.13278C>T (p.Asp4426=) rs777098264 0.00002
NM_001376.5(DYNC1H1):c.407G>A (p.Arg136Gln) rs996476189 0.00002
NM_001376.5(DYNC1H1):c.10241A>G (p.Asn3414Ser) rs1555411393 0.00001
NM_001376.5(DYNC1H1):c.10832G>A (p.Arg3611Gln) rs760957660 0.00001
NM_001376.5(DYNC1H1):c.11785G>A (p.Val3929Met) rs867293260 0.00001
NM_001376.5(DYNC1H1):c.12759C>T (p.Gly4253=) rs529010293 0.00001
NM_001376.5(DYNC1H1):c.1318A>C (p.Arg440=) rs1566997890 0.00001
NM_001376.5(DYNC1H1):c.13413C>T (p.Ala4471=) rs776463183 0.00001
NM_001376.5(DYNC1H1):c.3084T>G (p.Asp1028Glu) rs775528195 0.00001
NM_001376.5(DYNC1H1):c.3804G>A (p.Thr1268=) rs757595764 0.00001
NM_001376.5(DYNC1H1):c.4542+6G>A rs375822798 0.00001
NM_001376.5(DYNC1H1):c.7190G>A (p.Arg2397Gln) rs751820545 0.00001
NM_001376.5(DYNC1H1):c.8876A>G (p.Tyr2959Cys) rs797045536 0.00001
NM_001376.5(DYNC1H1):c.9975C>T (p.Cys3325=) rs1274600876 0.00001
NM_001376.5(DYNC1H1):c.10380C>T (p.Ala3460=) rs1555411404
NM_001376.5(DYNC1H1):c.10745G>T (p.Arg3582Leu) rs866994746
NM_001376.5(DYNC1H1):c.11045G>A (p.Arg3682Gln) rs1555411755
NM_001376.5(DYNC1H1):c.11245C>A (p.Leu3749Ile) rs1555411787
NM_001376.5(DYNC1H1):c.1151T>C (p.Ile384Thr)
NM_001376.5(DYNC1H1):c.11992C>T (p.Pro3998Ser) rs2152596268
NM_001376.5(DYNC1H1):c.12181G>A (p.Glu4061Lys) rs797045530
NM_001376.5(DYNC1H1):c.12428G>A (p.Arg4143His) rs867634752
NM_001376.5(DYNC1H1):c.13308G>T (p.Gln4436His)
NM_001376.5(DYNC1H1):c.13548G>C (p.Val4516=) rs1555412737
NM_001376.5(DYNC1H1):c.223C>T (p.His75Tyr)
NM_001376.5(DYNC1H1):c.2971A>G (p.Met991Val) rs1057518524
NM_001376.5(DYNC1H1):c.3795G>T (p.Lys1265Asn) rs1555408996
NM_001376.5(DYNC1H1):c.4140T>G (p.Tyr1380Ter) rs1567006190
NM_001376.5(DYNC1H1):c.4250T>C (p.Met1417Thr)
NM_001376.5(DYNC1H1):c.4289C>A (p.Thr1430Asn) rs1171366952
NM_001376.5(DYNC1H1):c.4580T>C (p.Leu1527Pro) rs879254213
NM_001376.5(DYNC1H1):c.4797_4798delinsTC (p.Arg1599_Ser1600delinsSerPro) rs2141287072
NM_001376.5(DYNC1H1):c.60C>G (p.Ala20=) rs1555407002
NM_001376.5(DYNC1H1):c.631C>G (p.Pro211Ala) rs1555407907
NM_001376.5(DYNC1H1):c.6406-4G>C rs374602014
NM_001376.5(DYNC1H1):c.6468G>A (p.Leu2156=) rs797045531
NM_001376.5(DYNC1H1):c.6857+6T>G rs1555409996
NM_001376.5(DYNC1H1):c.6997C>T (p.Leu2333Phe) rs1131691358
NM_001376.5(DYNC1H1):c.7072C>T (p.Arg2358Cys) rs879254019
NM_001376.5(DYNC1H1):c.7746C>T (p.Tyr2582=) rs797045533
NM_001376.5(DYNC1H1):c.7851G>A (p.Val2617=) rs1041508059
NM_001376.5(DYNC1H1):c.7884A>G (p.Pro2628=) rs797045534
NM_001376.5(DYNC1H1):c.791G>A (p.Arg264Gln) rs713993043
NM_001376.5(DYNC1H1):c.8209_8210insT (p.Asp2737fs)
NM_001376.5(DYNC1H1):c.948_952del (p.Phe316_Asp317insTer) rs1555407963
NM_001376.5(DYNC1H1):c.9960G>T (p.Ala3320=) rs746026558

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.