ClinVar Miner

List of variants in gene KIF1A reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 78
Download table as spreadsheet
HGVS dbSNP
NM_001244008.1(KIF1A):c.1684+17G>A rs574718771
NM_001244008.1(KIF1A):c.1A>G (p.Met1Val)
NM_001244008.1(KIF1A):c.2088C>T (p.Asn696=) rs758111969
NM_001244008.1(KIF1A):c.2494C>T (p.Pro832Ser) rs757726053
NM_001244008.1(KIF1A):c.2688C>T (p.Asp896=) rs1553632633
NM_001244008.1(KIF1A):c.2750_2751insTGAGGAGGAGGA (p.Glu916_Glu917insAspGluGluGlu) rs878988727
NM_001244008.1(KIF1A):c.3296A>G (p.Asn1099Ser)
NM_001244008.1(KIF1A):c.3759G>A (p.Pro1253=)
NM_001244008.1(KIF1A):c.4069C>T (p.Arg1357Trp) rs886042271
NM_001244008.1(KIF1A):c.420C>T (p.Tyr140=) rs1300729090
NM_001244008.1(KIF1A):c.4520G>A (p.Arg1507Gln)
NM_001244008.1(KIF1A):c.4554C>T (p.Ser1518=) rs775395101
NM_001244008.1(KIF1A):c.4694A>G (p.Asn1565Ser)
NM_001244008.1(KIF1A):c.4955G>A (p.Arg1652Gln) rs376658420
NM_004321.7(KIF1A):c.1038-6A>G rs1064796903
NM_004321.7(KIF1A):c.1063C>T (p.Arg355Cys) rs1225233710
NM_004321.7(KIF1A):c.1180+517G>A rs1553635398
NM_004321.7(KIF1A):c.1237C>T (p.Arg413Cys) rs374011613
NM_004321.7(KIF1A):c.1436A>T (p.Asp479Val) rs879253947
NM_004321.7(KIF1A):c.1551-4G>A rs376897164
NM_004321.7(KIF1A):c.1624G>A (p.Val542Ile) rs373891682
NM_004321.7(KIF1A):c.1636G>A (p.Asp546Asn) rs375972461
NM_004321.7(KIF1A):c.1809G>A (p.Glu603=) rs879254322
NM_004321.7(KIF1A):c.1829C>T (p.Ala610Val) rs765812659
NM_004321.7(KIF1A):c.1835C>T (p.Thr612Met) rs760338913
NM_004321.7(KIF1A):c.1966G>T (p.Ala656Ser) rs780686801
NM_004321.7(KIF1A):c.2039C>T (p.Ser680Phe) rs1553633725
NM_004321.7(KIF1A):c.2242C>G (p.Gln748Glu) rs369410320
NM_004321.7(KIF1A):c.2506G>T (p.Gly836Cys) rs761671317
NM_004321.7(KIF1A):c.2509G>A (p.Gly837Arg) rs768702963
NM_004321.7(KIF1A):c.2555+863G>A rs1064796756
NM_004321.7(KIF1A):c.2555+899G>A rs763933124
NM_004321.7(KIF1A):c.2555+996G>A rs192102667
NM_004321.7(KIF1A):c.2631C>T (p.Gly877=) rs751977290
NM_004321.7(KIF1A):c.2674+5G>A rs200583714
NM_004321.7(KIF1A):c.2707G>A (p.Val903Ile) rs763669401
NM_004321.7(KIF1A):c.2750A>G (p.His917Arg) rs201846946
NM_004321.7(KIF1A):c.2764C>T (p.Gln922Ter) rs1426121066
NM_004321.7(KIF1A):c.2798G>T (p.Arg933Leu) rs375775494
NM_004321.7(KIF1A):c.2857G>A (p.Val953Met) rs371233697
NM_004321.7(KIF1A):c.2899+10C>A rs190997558
NM_004321.7(KIF1A):c.3027G>A (p.Ala1009=) rs200149062
NM_004321.7(KIF1A):c.3042C>G (p.Ala1014=) rs370286749
NM_004321.7(KIF1A):c.3191T>C (p.Ile1064Thr) rs35698242
NM_004321.7(KIF1A):c.3296C>T (p.Ser1099Leu) rs763750448
NM_004321.7(KIF1A):c.3313C>T (p.Arg1105Trp) rs772443183
NM_004321.7(KIF1A):c.3343G>A (p.Ala1115Thr) rs368057315
NM_004321.7(KIF1A):c.3371C>G (p.Pro1124Arg) rs377389267
NM_004321.7(KIF1A):c.3390C>T (p.His1130=) rs375829173
NM_004321.7(KIF1A):c.3583C>G (p.Arg1195Gly) rs201684653
NM_004321.7(KIF1A):c.3617C>T (p.Pro1206Leu) rs1085307567
NM_004321.7(KIF1A):c.3625G>A (p.Asp1209Asn) rs371252476
NM_004321.7(KIF1A):c.3676G>A (p.Gly1226Arg) rs879253904
NM_004321.7(KIF1A):c.3728C>T (p.Ala1243Val) rs876661146
NM_004321.7(KIF1A):c.3905G>A (p.Arg1302His) rs537708830
NM_004321.7(KIF1A):c.3946T>A (p.Ser1316Thr) rs200855792
NM_004321.7(KIF1A):c.3994G>A (p.Val1332Met) rs879253922
NM_004321.7(KIF1A):c.41C>T (p.Pro14Leu) rs879253976
NM_004321.7(KIF1A):c.4208C>T (p.Thr1403Ile) rs371831198
NM_004321.7(KIF1A):c.4241C>T (p.Pro1414Leu) rs867230401
NM_004321.7(KIF1A):c.4301C>T (p.Ala1434Val) rs141441058
NM_004321.7(KIF1A):c.4405C>T (p.His1469Tyr) rs528171871
NM_004321.7(KIF1A):c.4468C>T (p.Arg1490Trp) rs201139273
NM_004321.7(KIF1A):c.4478C>T (p.Ser1493Leu) rs201825284
NM_004321.7(KIF1A):c.4624G>A (p.Asp1542Asn) rs200141437
NM_004321.7(KIF1A):c.4668C>A (p.Asp1556Glu) rs184939069
NM_004321.7(KIF1A):c.4712G>A (p.Arg1571Gln) rs761974755
NM_004321.7(KIF1A):c.4726G>A (p.Val1576Ile) rs757070178
NM_004321.7(KIF1A):c.4784G>A (p.Arg1595His) rs756912340
NM_004321.7(KIF1A):c.4799G>A (p.Arg1600Gln) rs780828140
NM_004321.7(KIF1A):c.4828G>A (p.Asp1610Asn) rs199574770
NM_004321.7(KIF1A):c.4852G>A (p.Val1618Met) rs200511467
NM_004321.7(KIF1A):c.4864G>A (p.Ala1622Thr) rs879253903
NM_004321.7(KIF1A):c.4865C>T (p.Ala1622Val) rs199804623
NM_004321.7(KIF1A):c.502G>A (p.Val168Met) rs1057519241
NM_004321.7(KIF1A):c.536A>G (p.Glu179Gly) rs879253948
NM_004321.7(KIF1A):c.720+5G>C rs377502239
NM_004321.7(KIF1A):c.850G>A (p.Ala284Thr) rs756136593

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.