ClinVar Miner

List of variants in gene KIF5A reported as benign

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Gene type:
ClinVar version:
Total variants: 77
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HGVS dbSNP gnomAD frequency
NM_004984.4(KIF5A):c.2910-83A>G rs775247 0.99188
NM_004984.4(KIF5A):c.2993-217G>A rs809593 0.89528
NM_004984.4(KIF5A):c.1717-129G>A rs11172254 0.45208
NM_004984.4(KIF5A):c.714+93T>C rs10783832 0.44388
NM_004984.4(KIF5A):c.714+161A>G rs10783833 0.44255
NM_004984.4(KIF5A):c.445+22A>G rs775322 0.41472
NM_004984.4(KIF5A):c.1717-152C>G rs1678542 0.41355
NM_004984.4(KIF5A):c.3020+235C>G rs2888334 0.27833
NM_004984.4(KIF5A):c.2992+218G>C rs10783834 0.27821
NM_004984.4(KIF5A):c.36+42C>A rs775250 0.25466
NM_004984.4(KIF5A):c.2992+175C>G rs775248 0.25365
NM_004984.4(KIF5A):c.36+5C>T rs775249 0.25100
NM_004984.4(KIF5A):c.2993-267A>G rs11172256 0.19121
NM_004984.4(KIF5A):c.2539-69G>A rs775245 0.12403
NM_004984.4(KIF5A):c.819+94G>C rs2620678 0.03641
NM_004984.4(KIF5A):c.129+310C>T rs73346031 0.02913
NM_004984.4(KIF5A):c.*163C>T rs77345621 0.02715
NM_004984.4(KIF5A):c.445+73A>G rs75527218 0.02640
NC_000012.12:g.57549736C>T rs79749420 0.02376
NM_004984.4(KIF5A):c.292-170G>A rs115447581 0.01971
NM_004984.4(KIF5A):c.2957C>T (p.Pro986Leu) rs113247976 0.01241
NM_004984.4(KIF5A):c.*394A>G rs114621289 0.00866
NM_004984.4(KIF5A):c.2023+18C>T rs192960012 0.00832
NM_004984.4(KIF5A):c.820-19G>T rs181688415 0.00736
NM_004984.4(KIF5A):c.396+14G>A rs17119769 0.00700
NM_004984.4(KIF5A):c.2769G>A (p.Arg923=) rs35225609 0.00394
NM_004984.4(KIF5A):c.446-18T>C rs188999300 0.00237
NM_004984.4(KIF5A):c.2088+21G>A rs200230112 0.00225
NM_004984.4(KIF5A):c.1293+9G>A rs201749114 0.00222
NM_004984.4(KIF5A):c.*425C>T rs180971201 0.00198
NM_004984.4(KIF5A):c.2433+19G>A rs114929380 0.00170
NM_004984.4(KIF5A):c.2839A>G (p.Thr947Ala) rs150672943 0.00117
NM_004984.4(KIF5A):c.714+8G>A rs199624091 0.00101
NM_004984.4(KIF5A):c.2418G>A (p.Thr806=) rs113155897 0.00100
NM_004984.4(KIF5A):c.2199-4G>A rs201366820 0.00077
NM_004984.4(KIF5A):c.2272G>A (p.Glu758Lys) rs140281678 0.00074
NM_004984.4(KIF5A):c.1419G>A (p.Leu473=) rs139091551 0.00070
NM_004984.4(KIF5A):c.1105C>T (p.Arg369Trp) rs140929639 0.00056
NM_004984.4(KIF5A):c.2403C>T (p.Phe801=) rs149934878 0.00054
NM_004984.4(KIF5A):c.2412C>T (p.Asp804=) rs145062338 0.00038
NM_004984.4(KIF5A):c.471C>T (p.His157=) rs143178113 0.00034
NM_004984.4(KIF5A):c.60C>T (p.Asn20=) rs200876187 0.00021
NM_004984.4(KIF5A):c.2832C>T (p.Ile944=) rs114935472 0.00020
NM_004984.4(KIF5A):c.1294-10C>A rs530832211 0.00019
NM_004984.4(KIF5A):c.2040G>A (p.Val680=) rs117670788 0.00016
NM_004984.4(KIF5A):c.292-5G>A rs201917057 0.00016
NM_004984.4(KIF5A):c.152G>A (p.Arg51His) rs773336059 0.00010
NM_004984.4(KIF5A):c.2023+14A>G rs750746685 0.00009
NM_004984.4(KIF5A):c.820-9C>A rs185306438 0.00007
NM_004984.4(KIF5A):c.715-20A>G rs201888198 0.00006
NM_004984.4(KIF5A):c.1368G>A (p.Leu456=) rs769470445 0.00005
NM_004984.4(KIF5A):c.1281G>A (p.Gln427=) rs771610789 0.00004
NM_004984.4(KIF5A):c.341G>A (p.Arg114Gln) rs144277716 0.00004
NM_004984.4(KIF5A):c.2217G>C (p.Gln739His) rs755813386 0.00002
NM_004984.4(KIF5A):c.2538+8T>G rs377005699 0.00002
NM_004984.4(KIF5A):c.2993-12T>C rs542701424 0.00002
NM_004984.4(KIF5A):c.2024-8T>G rs190187837 0.00001
NM_004984.4(KIF5A):c.531G>A (p.Pro177=) rs771476833 0.00001
NM_004984.4(KIF5A):c.*36+95dup rs35104895
NM_004984.4(KIF5A):c.1058C>G (p.Thr353Arg)
NM_004984.4(KIF5A):c.1087C>T (p.Leu363=)
NM_004984.4(KIF5A):c.1118-8del
NM_004984.4(KIF5A):c.1176G>A (p.Glu392=) rs75907338
NM_004984.4(KIF5A):c.1548G>A (p.Val516=)
NM_004984.4(KIF5A):c.2089-11del
NM_004984.4(KIF5A):c.2756-43A>C rs775246
NM_004984.4(KIF5A):c.2992+12dup rs576635518
NM_004984.4(KIF5A):c.3020+215C>G
NM_004984.4(KIF5A):c.3020+22del rs751099911
NM_004984.4(KIF5A):c.397-16_397-14del rs375316447
NM_004984.4(KIF5A):c.589+20del rs2140161312
NM_004984.4(KIF5A):c.714+59_714+60del rs371727146
NM_004984.4(KIF5A):c.714+60del rs371727146
NM_004984.4(KIF5A):c.714+60dup rs371727146
NM_004984.4(KIF5A):c.715-225dup rs558633353
NM_004984.4(KIF5A):c.820-3del rs1349311406
NM_004984.4(KIF5A):c.968+8G>T

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