ClinVar Miner

List of variants in gene KIF1A reported as likely benign by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 34
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HGVS dbSNP
NM_004321.7(KIF1A):c.*1005G>A rs58502378
NM_004321.7(KIF1A):c.*1187C>T rs3732342
NM_004321.7(KIF1A):c.*1237C>T rs3732341
NM_004321.7(KIF1A):c.*1685G>C rs3732340
NM_004321.7(KIF1A):c.*1686G>C rs142220621
NM_004321.7(KIF1A):c.*1694C>T rs3732339
NM_004321.7(KIF1A):c.*1743G>A rs3732338
NM_004321.7(KIF1A):c.*1823C>T rs7566538
NM_004321.7(KIF1A):c.*2257C>T rs11547136
NM_004321.7(KIF1A):c.*2543C>T rs141926687
NM_004321.7(KIF1A):c.*2576A>G rs79286402
NM_004321.7(KIF1A):c.*3038T>A rs116352370
NM_004321.7(KIF1A):c.*3494T>C rs4613
NM_004321.7(KIF1A):c.*3596C>T rs143001518
NM_004321.7(KIF1A):c.1476A>G (p.Pro492=) rs35663732
NM_004321.7(KIF1A):c.183+15C>T rs73102676
NM_004321.7(KIF1A):c.184-10C>T rs7594776
NM_004321.7(KIF1A):c.2208C>T (p.Ala736=) rs35945835
NM_004321.7(KIF1A):c.234C>T (p.Gly78=) rs61744930
NM_004321.7(KIF1A):c.2358C>T (p.Ala786=) rs62637652
NM_004321.7(KIF1A):c.2448C>T (p.Tyr816=) rs199996308
NM_004321.7(KIF1A):c.2674+13C>T rs116600932
NM_004321.7(KIF1A):c.2676C>T (p.Ala892=) rs116297894
NM_004321.7(KIF1A):c.2769C>T (p.Ser923=) rs73102625
NM_004321.7(KIF1A):c.2979C>T (p.His993=) rs35664935
NM_004321.7(KIF1A):c.3338-8C>T rs56024577
NM_004321.7(KIF1A):c.3549T>C (p.His1183=) rs184931664
NM_004321.7(KIF1A):c.3598+11T>C rs56847463
NM_004321.7(KIF1A):c.3840G>A (p.Pro1280=) rs2241683
NM_004321.7(KIF1A):c.393C>T (p.Asn131=) rs35139906
NM_004321.7(KIF1A):c.4016-8C>T rs1529663
NM_004321.7(KIF1A):c.4509C>A (p.Thr1503=) rs76974316
NM_004321.7(KIF1A):c.4586G>A (p.Arg1529Gln) rs191428830
NM_004321.7(KIF1A):c.991T>C (p.Leu331=) rs1063353

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