ClinVar Miner

List of variants in gene KIF21A reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 55
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001173464.2(KIF21A):c.*472A>G rs11171674 0.29577
NM_001173464.2(KIF21A):c.*237A>G rs11171675 0.29569
NM_017641.3(KIF21A):c.-313G>A rs11835359 0.06971
NM_001173464.2(KIF21A):c.*418A>G rs77242017 0.06929
NM_001173464.2(KIF21A):c.4768C>T (p.Leu1590=) rs2271477 0.05003
NM_001173464.2(KIF21A):c.3711G>T (p.Glu1237Asp) rs75223821 0.04314
NM_001173464.2(KIF21A):c.1880G>T (p.Gly627Val) rs79089655 0.03351
NM_017641.3(KIF21A):c.-165G>T rs111306046 0.03008
NM_001173464.2(KIF21A):c.1335G>T (p.Thr445=) rs61740919 0.01740
NM_001173464.2(KIF21A):c.1628A>G (p.Lys543Arg) rs149219011 0.00766
NM_001173464.2(KIF21A):c.1469+10A>G rs73266501 0.00562
NM_001173464.2(KIF21A):c.2541A>G (p.Lys847=) rs145897823 0.00402
NM_001173464.2(KIF21A):c.*447A>G rs74088336 0.00401
NM_001173464.2(KIF21A):c.4542C>G (p.Ser1514=) rs11171689 0.00359
NM_017641.3(KIF21A):c.-210C>T rs113038492 0.00288
NM_001173464.2(KIF21A):c.3149A>G (p.Asn1050Ser) rs142268373 0.00239
NM_001173464.2(KIF21A):c.1240G>C (p.Gly414Arg) rs78616703 0.00229
NM_001173464.2(KIF21A):c.903T>A (p.Leu301=) rs78806233 0.00220
NM_001173464.2(KIF21A):c.3332T>C (p.Val1111Ala) rs150294289 0.00179
NM_001173464.2(KIF21A):c.*707A>G rs536139187 0.00159
NM_001173464.2(KIF21A):c.1713-11C>G rs142304324 0.00142
NM_001173464.2(KIF21A):c.-19A>G rs139423015 0.00135
NM_001173464.2(KIF21A):c.3118C>T (p.Leu1040=) rs79512568 0.00135
NM_001173464.2(KIF21A):c.3641C>G (p.Pro1214Arg) rs149075970 0.00092
NM_001173464.2(KIF21A):c.*812T>C rs532231850 0.00090
NM_017641.3(KIF21A):c.-240G>C rs562588358 0.00089
NM_017641.3(KIF21A):c.-257C>A rs529777052 0.00088
NM_001173464.2(KIF21A):c.4515T>G (p.Ser1505Arg) rs62000373 0.00087
NM_001173464.2(KIF21A):c.2487+5A>T rs376142046 0.00083
NM_001173464.2(KIF21A):c.*645T>G rs554887830 0.00071
NM_001173464.2(KIF21A):c.1038A>G (p.Ala346=) rs148354450 0.00064
NM_001173464.2(KIF21A):c.975T>C (p.Asp325=) rs143790968 0.00045
NM_001173464.2(KIF21A):c.3959G>A (p.Arg1320Lys) rs142879430 0.00044
NM_001173464.2(KIF21A):c.4536T>C (p.Thr1512=) rs144103791 0.00042
NM_001173464.2(KIF21A):c.2684C>T (p.Pro895Leu) rs149718388 0.00039
NM_001173464.2(KIF21A):c.3111C>T (p.Ala1037=) rs145404005 0.00036
NM_001173464.2(KIF21A):c.1776G>A (p.Ser592=) rs143782701 0.00031
NM_001173464.2(KIF21A):c.2660C>T (p.Ala887Val) rs145318959 0.00027
NM_001173464.2(KIF21A):c.4044A>G (p.Lys1348=) rs201297981 0.00022
NM_001173464.2(KIF21A):c.608A>G (p.Gln203Arg) rs149328427 0.00021
NM_001173464.2(KIF21A):c.1804-15C>T rs376342352 0.00016
NM_001173464.2(KIF21A):c.2305A>G (p.Thr769Ala) rs200645253 0.00014
NM_001173464.2(KIF21A):c.4562T>G (p.Met1521Arg) rs142038295 0.00009
NM_001173464.2(KIF21A):c.1160A>G (p.Asn387Ser) rs745692702 0.00006
NM_001173464.2(KIF21A):c.1886G>T (p.Ser629Ile) rs765856120 0.00004
NM_001173464.2(KIF21A):c.2310+10A>G rs201113357 0.00003
NM_001173464.2(KIF21A):c.-31C>T rs554379231 0.00001
NM_001173464.2(KIF21A):c.1104T>G (p.Ala368=) rs187327535 0.00001
NM_001173464.2(KIF21A):c.3842G>A (p.Arg1281His) rs747176706 0.00001
NM_001173464.2(KIF21A):c.3960-11C>T rs201115347 0.00001
NM_001173464.2(KIF21A):c.578G>A (p.Arg193His) rs770064077 0.00001
NM_001173464.2(KIF21A):c.*690del rs34373131
NM_001173464.2(KIF21A):c.1458C>A (p.Ile486=) rs200512673
NM_017641.3(KIF21A):c.-195A>G rs532130145
NM_017641.3(KIF21A):c.-411G>A rs145372857

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.