ClinVar Miner

List of variants in gene KIF21A reported as benign for hereditary skeletal muscle disorder

Included ClinVar conditions (591):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
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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.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.1038A>G (p.Ala346=) rs148354450 0.00041
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.1886G>T (p.Ser629Ile) rs765856120 0.00004
NM_001173464.2(KIF21A):c.2310+10A>G rs201113357 0.00003
NM_001173464.2(KIF21A):c.1160A>G (p.Asn387Ser) rs745692702 0.00002
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_001173464.2(KIF21A):c.3301C>A (p.Leu1101Ile)
NM_017641.3(KIF21A):c.-195A>G rs532130145
NM_017641.3(KIF21A):c.-411G>A rs145372857

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