ClinVar Miner

List of variants in gene KIF1B reported as uncertain significance for not provided

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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_001365951.3(KIF1B):c.2115+6753A>G rs41274462 0.01960
NM_001365951.3(KIF1B):c.2115+7031T>C rs149267056 0.00320
NM_001365951.3(KIF1B):c.2115+6625G>A rs145248590 0.00129
NM_001365951.3(KIF1B):c.3645G>A (p.Pro1215=) rs147318592 0.00092
NM_001365951.3(KIF1B):c.2115+6581G>A rs41274460 0.00089
NM_001365951.3(KIF1B):c.2551T>A (p.Leu851Met) rs139572764 0.00046
NM_001365951.3(KIF1B):c.2618C>T (p.Thr873Ile) rs121908162 0.00040
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.2115+6835C>T rs140733878 0.00026
NM_001365951.3(KIF1B):c.2159C>T (p.Thr720Ile) rs41274468 0.00024
NM_001365951.3(KIF1B):c.4211T>C (p.Val1404Ala) rs200561798 0.00022
NM_001365951.3(KIF1B):c.4516G>A (p.Glu1506Lys) rs754226097 0.00014
NM_001365951.3(KIF1B):c.1594C>G (p.Pro532Ala) rs201500946 0.00013
NM_001365951.3(KIF1B):c.146C>A (p.Ser49Tyr) rs143654307 0.00009
NM_001365951.3(KIF1B):c.899A>G (p.Lys300Arg) rs373698346 0.00009
NM_001365951.3(KIF1B):c.1769G>A (p.Ser590Asn) rs768672234 0.00006
NM_001365951.3(KIF1B):c.2001G>A (p.Leu667=) rs543345616 0.00006
NM_001365951.3(KIF1B):c.2115+6205C>T rs771399291 0.00006
NM_001365951.3(KIF1B):c.2115+6A>T rs149407490 0.00006
NM_001365951.3(KIF1B):c.2675+3A>G rs200684032 0.00006
NM_001365951.3(KIF1B):c.4265G>A (p.Arg1422His) rs149417293 0.00006
NM_001365951.3(KIF1B):c.4810G>A (p.Val1604Ile) rs769092155 0.00004
NM_001365951.3(KIF1B):c.2115+6805C>G rs377168351 0.00003
NM_001365951.3(KIF1B):c.2605G>A (p.Glu869Lys) rs370243199 0.00002
NM_001365951.3(KIF1B):c.3119A>G (p.Tyr1040Cys) rs751434716 0.00002
NM_001365951.3(KIF1B):c.3925A>G (p.Lys1309Glu) rs772177176 0.00002
NM_001365951.3(KIF1B):c.5039G>A (p.Arg1680Gln) rs775552504 0.00002
NM_001365951.3(KIF1B):c.5053G>A (p.Glu1685Lys) rs764494187 0.00002
NM_001365951.3(KIF1B):c.5423G>A (p.Arg1808His) rs770215708 0.00002
NM_001365951.3(KIF1B):c.1010A>G (p.Asn337Ser) rs759806939 0.00001
NM_001365951.3(KIF1B):c.1751G>T (p.Arg584Leu) rs1169892801 0.00001
NM_001365951.3(KIF1B):c.2115+6376A>G rs1314929841 0.00001
NM_001365951.3(KIF1B):c.2115+7126C>T rs1035620392 0.00001
NM_001365951.3(KIF1B):c.3625C>G (p.Leu1209Val) rs1320246121 0.00001
NM_001365951.3(KIF1B):c.4444C>T (p.Arg1482Trp) rs1461624745 0.00001
NM_001365951.3(KIF1B):c.4633A>G (p.Ile1545Val) rs148387809 0.00001
NM_001365951.3(KIF1B):c.4849C>T (p.Arg1617Trp) rs765259892 0.00001
NM_001365951.3(KIF1B):c.5014G>C (p.Ala1672Pro) rs909290817 0.00001
NM_001365951.3(KIF1B):c.5036C>G (p.Ala1679Gly) rs776751303 0.00001
NM_001365951.3(KIF1B):c.5063A>G (p.Asn1688Ser) rs866721796 0.00001
GRCh37/hg19 1p36.22(chr1:10371763-10401671)x1
NM_001365951.3(KIF1B):c.1109G>A (p.Arg370His) rs764203468
NM_001365951.3(KIF1B):c.1171A>G (p.Ile391Val) rs754483212
NM_001365951.3(KIF1B):c.1434+5G>A rs1064797106
NM_001365951.3(KIF1B):c.1487G>A (p.Arg496His) rs1418377932
NM_001365951.3(KIF1B):c.1515-18T>G rs375149695
NM_001365951.3(KIF1B):c.1624C>G (p.Leu542Val) rs1557694736
NM_001365951.3(KIF1B):c.2043-10_2043-9del rs58344165
NM_001365951.3(KIF1B):c.2115+12G>C rs746838721
NM_001365951.3(KIF1B):c.2115+5955_2115+5958dup rs1569771586
NM_001365951.3(KIF1B):c.2115+7148C>T
NM_001365951.3(KIF1B):c.2115+7154C>G rs866635609
NM_001365951.3(KIF1B):c.2386G>A (p.Asp796Asn) rs1057523099
NM_001365951.3(KIF1B):c.2612A>G (p.Glu871Gly)
NM_001365951.3(KIF1B):c.3079C>T (p.Arg1027Ter) rs886042662
NM_001365951.3(KIF1B):c.3148G>C (p.Ala1050Pro) rs77581495
NM_001365951.3(KIF1B):c.3304G>A (p.Gly1102Arg) rs751916846
NM_001365951.3(KIF1B):c.3644C>A (p.Pro1215Gln) rs369255811
NM_001365951.3(KIF1B):c.4066C>T (p.Arg1356Cys) rs1231187230
NM_001365951.3(KIF1B):c.430-9del rs771477893
NM_001365951.3(KIF1B):c.4508A>T (p.His1503Leu) rs1224742258
NM_001365951.3(KIF1B):c.4570A>G (p.Lys1524Glu) rs2102350303
NM_001365951.3(KIF1B):c.4576C>G (p.Leu1526Val)
NM_001365951.3(KIF1B):c.4586C>T (p.Ser1529Leu) rs781051649
NM_001365951.3(KIF1B):c.5079T>C (p.Ile1693=)

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