ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 50
Download table as spreadsheet
HGVS dbSNP
NM_001244008.1(KIF1A):c.2721_2723GGA[9] (p.Glu916_Glu917del) rs10594016
NM_004321.7(KIF1A):c.1336G>C (p.Glu446Gln) rs777894370
NM_004321.7(KIF1A):c.1636G>A (p.Asp546Asn) rs375972461
NM_004321.7(KIF1A):c.1835C>T (p.Thr612Met) rs760338913
NM_004321.7(KIF1A):c.203C>T (p.Ala68Val) rs550027484
NM_004321.7(KIF1A):c.2061C>T (p.Asn687=) rs758111969
NM_004321.7(KIF1A):c.2105G>A (p.Arg702Gln) rs774604596
NM_004321.7(KIF1A):c.2448C>T (p.Tyr816=) rs199996308
NM_004321.7(KIF1A):c.2505C>T (p.Thr835=) rs370648599
NM_004321.7(KIF1A):c.2595C>G (p.Pro865=) rs140783695
NM_004321.7(KIF1A):c.2605C>T (p.Arg869Cys) rs864309570
NM_004321.7(KIF1A):c.2651G>A (p.Arg884His) rs772779524
NM_004321.7(KIF1A):c.2655G>C (p.Val885=) rs186881889
NM_004321.7(KIF1A):c.2801C>T (p.Ser934Leu) rs764873243
NM_004321.7(KIF1A):c.2916_2918CCT[2] (p.Leu975del) rs1167417315
NM_004321.7(KIF1A):c.2943C>T (p.Ala981=) rs368682964
NM_004321.7(KIF1A):c.3042C>G (p.Ala1014=) rs370286749
NM_004321.7(KIF1A):c.3072C>T (p.Asn1024=) rs1380599495
NM_004321.7(KIF1A):c.311C>T (p.Ser104Phe) rs1553639010
NM_004321.7(KIF1A):c.3165C>T (p.Ile1055=) rs201981364
NM_004321.7(KIF1A):c.3365C>T (p.Thr1122Met) rs374873057
NM_004321.7(KIF1A):c.3377C>T (p.Pro1126Leu) rs374244985
NM_004321.7(KIF1A):c.3585C>T (p.Arg1195=) rs144520412
NM_004321.7(KIF1A):c.3595G>A (p.Val1199Met) rs797045652
NM_004321.7(KIF1A):c.3701A>G (p.Asp1234Gly) rs747271930
NM_004321.7(KIF1A):c.3914G>A (p.Arg1305His) rs755301795
NM_004321.7(KIF1A):c.408C>G (p.Asp136Glu) rs761179236
NM_004321.7(KIF1A):c.4252G>A (p.Glu1418Lys) rs769965899
NM_004321.7(KIF1A):c.4282G>A (p.Ala1428Thr) rs572923181
NM_004321.7(KIF1A):c.4301C>T (p.Ala1434Val) rs141441058
NM_004321.7(KIF1A):c.4335C>T (p.Asn1445=) rs771217469
NM_004321.7(KIF1A):c.4362+4G>C rs772449700
NM_004321.7(KIF1A):c.4413C>T (p.His1471=) rs375640417
NM_004321.7(KIF1A):c.4475C>T (p.Pro1492Leu) rs200902828
NM_004321.7(KIF1A):c.4478C>T (p.Ser1493Leu) rs201825284
NM_004321.7(KIF1A):c.4510C>T (p.Pro1504Ser) rs916993059
NM_004321.7(KIF1A):c.4586G>A (p.Arg1529Gln) rs191428830
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.4714G>A (p.Val1572Ile) rs774256831
NM_004321.7(KIF1A):c.4718+1G>C rs797045653
NM_004321.7(KIF1A):c.4740G>A (p.Gly1580=) rs143815273
NM_004321.7(KIF1A):c.4789G>A (p.Val1597Met) rs769279843
NM_004321.7(KIF1A):c.5019C>T (p.Ala1673=) rs745898229
NM_004321.7(KIF1A):c.560C>T (p.Thr187Ile) rs370623844
NM_004321.7(KIF1A):c.609-8C>T rs775915390
NM_004321.7(KIF1A):c.666C>T (p.Asn222=) rs797045654
NM_004321.7(KIF1A):c.829_849del (p.Thr277_Ser283del) rs1057518407
NM_004321.7(KIF1A):c.849C>T (p.Ser283=) rs187442951
NM_004321.7(KIF1A):c.883-3C>T rs111507743

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.