ClinVar Miner

List of variants in gene KIF1B reported by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP gnomAD frequency
NM_001365951.3(KIF1B):c.1777+10C>T rs3753037 0.26503
NM_001365951.3(KIF1B):c.720+17C>T rs1339458 0.25792
NM_001365951.3(KIF1B):c.285C>G (p.Ala95=) rs12402052 0.24010
NM_001365951.3(KIF1B):c.5301C>A (p.Thr1767=) rs11121552 0.23676
NM_001365951.3(KIF1B):c.4299A>G (p.Pro1433=) rs12125492 0.08850
NM_001365951.3(KIF1B):c.1180+18C>T rs41274456 0.03074
NM_001365951.3(KIF1B):c.2115+6207G>A rs75760005 0.02849
NM_001365951.3(KIF1B):c.608+8dup rs139613776 0.01962
NM_001365951.3(KIF1B):c.363+6A>C rs114084418 0.01751
NM_001365951.3(KIF1B):c.4798G>A (p.Val1600Met) rs77172218 0.01096
NM_001365951.3(KIF1B):c.2115+6956A>G rs148481786 0.00525
NM_001365951.3(KIF1B):c.4158G>A (p.Ser1386=) rs116302604 0.00481
NM_001365951.3(KIF1B):c.2970C>A (p.Ile990=) rs78611156 0.00200
NM_001365951.3(KIF1B):c.*2T>C rs148690591 0.00185
NM_001365951.3(KIF1B):c.2115+6625G>A rs145248590 0.00129
NM_001365951.3(KIF1B):c.2115+5958G>A rs150181429 0.00050
NM_001365951.3(KIF1B):c.2551T>A (p.Leu851Met) rs139572764 0.00046
NM_001365951.3(KIF1B):c.4356A>G (p.Thr1452=) rs150358670 0.00038
NM_001365951.3(KIF1B):c.2604C>T (p.Asp868=) rs145846362 0.00031
NM_001365951.3(KIF1B):c.2115+7081C>T rs376558549 0.00029
NM_001365951.3(KIF1B):c.2115+6313G>A rs374263753 0.00028
NM_001365951.3(KIF1B):c.1771G>A (p.Gly591Arg) rs145266399 0.00024
NM_001365951.3(KIF1B):c.1014C>T (p.Tyr338=) rs150411706 0.00019
NM_001365951.3(KIF1B):c.2985C>T (p.Ile995=) rs150904940 0.00018
NM_001365951.3(KIF1B):c.3131G>A (p.Ser1044Asn) rs769602520 0.00016
NM_001365951.3(KIF1B):c.4855C>G (p.Pro1619Ala) rs146177892 0.00016
NM_001365951.3(KIF1B):c.4946+10C>T rs374982816 0.00014
NM_001365951.3(KIF1B):c.4820G>A (p.Cys1607Tyr) rs145969842 0.00013
NM_001365951.3(KIF1B):c.2593A>C (p.Ser865Arg) rs140015591 0.00011
NM_001365951.3(KIF1B):c.5238C>T (p.Asn1746=) rs146436697 0.00009
NM_001365951.3(KIF1B):c.1557T>C (p.Asp519=) rs146364486 0.00007
NM_001365951.3(KIF1B):c.107-8T>A rs749389756 0.00006
NM_001365951.3(KIF1B):c.4668C>T (p.Ser1556=) rs765541693 0.00006
NM_001365951.3(KIF1B):c.3959G>A (p.Arg1320Gln) rs371798689 0.00004
NM_001365951.3(KIF1B):c.1122G>A (p.Glu374=) rs774770887 0.00003
NM_001365951.3(KIF1B):c.1867C>T (p.Arg623Cys) rs150271500 0.00003
NM_001365951.3(KIF1B):c.4281C>T (p.Ser1427=) rs148438684 0.00003
NM_001365951.3(KIF1B):c.4683C>T (p.Ser1561=) rs751084365 0.00002
NM_001365951.3(KIF1B):c.1435-9C>T rs200798756 0.00001
NM_001365951.3(KIF1B):c.1515-5C>T rs776534234 0.00001
NM_001365951.3(KIF1B):c.1680A>G (p.Gln560=) rs765720258 0.00001
NM_001365951.3(KIF1B):c.3513+7G>T rs1174031782 0.00001
NM_001365951.3(KIF1B):c.1194C>T (p.Ile398=)
NM_001365951.3(KIF1B):c.1195G>A (p.Asp399Asn)
NM_001365951.3(KIF1B):c.1256A>G (p.Tyr419Cys)
NM_001365951.3(KIF1B):c.1263A>G (p.Leu421=)
NM_001365951.3(KIF1B):c.1590+6A>G
NM_001365951.3(KIF1B):c.184-6_184-5del rs138324955
NM_001365951.3(KIF1B):c.1968T>C (p.Pro656=) rs1332046524
NM_001365951.3(KIF1B):c.2115+5919C>T
NM_001365951.3(KIF1B):c.2115+5921C>T
NM_001365951.3(KIF1B):c.2115+6104G>A
NM_001365951.3(KIF1B):c.2115+6327C>T
NM_001365951.3(KIF1B):c.2115+6400G>T
NM_001365951.3(KIF1B):c.2115+6485del
NM_001365951.3(KIF1B):c.2115+6587G>A
NM_001365951.3(KIF1B):c.2115+6733T>C
NM_001365951.3(KIF1B):c.2115+6813C>A
NM_001365951.3(KIF1B):c.2115+6912A>G
NM_001365951.3(KIF1B):c.2115+6940_2115+6942del
NM_001365951.3(KIF1B):c.2115+7077A>G
NM_001365951.3(KIF1B):c.2115+7132C>G
NM_001365951.3(KIF1B):c.2115+7188T>C
NM_001365951.3(KIF1B):c.2115+7213C>T
NM_001365951.3(KIF1B):c.2275T>C (p.Phe759Leu)
NM_001365951.3(KIF1B):c.253G>A (p.Ala85Thr)
NM_001365951.3(KIF1B):c.285C>T (p.Ala95=)
NM_001365951.3(KIF1B):c.3044-10del rs758417740
NM_001365951.3(KIF1B):c.3157C>T (p.Arg1053Cys)
NM_001365951.3(KIF1B):c.3198A>G (p.Gly1066=)
NM_001365951.3(KIF1B):c.3560A>G (p.Lys1187Arg)
NM_001365951.3(KIF1B):c.3830G>A (p.Gly1277Asp)
NM_001365951.3(KIF1B):c.3934C>T (p.Arg1312Cys)
NM_001365951.3(KIF1B):c.430-9del rs771477893
NM_001365951.3(KIF1B):c.4479G>A (p.Gln1493=) rs1638533963
NM_001365951.3(KIF1B):c.4662T>C (p.Phe1554=)
NM_001365951.3(KIF1B):c.5096+7A>G
NM_001365951.3(KIF1B):c.5234T>G (p.Ile1745Ser)
NM_001365951.3(KIF1B):c.525A>T (p.Gly175=)
NM_001365951.3(KIF1B):c.865-4G>T

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