ClinVar Miner

List of variants in gene KIF1B reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_001365951.3(KIF1B):c.3423-15del rs3215996 0.03458
NM_001365951.3(KIF1B):c.608+8dup rs139613776 0.01962
NM_001365951.3(KIF1B):c.*4325G>A rs141688466 0.00419
NM_001365951.3(KIF1B):c.5020G>A (p.Glu1674Lys) rs143669846 0.00317
NM_001365951.3(KIF1B):c.*4113C>T rs192312673 0.00285
NM_001365951.3(KIF1B):c.*3930C>T rs549049444 0.00216
NM_001365951.3(KIF1B):c.*3035G>A rs41301987 0.00126
NM_001365951.3(KIF1B):c.3645G>A (p.Pro1215=) rs147318592 0.00092
NM_001365951.3(KIF1B):c.*1238G>A rs539372635 0.00058
NM_001365951.3(KIF1B):c.1435-15C>T rs371838261 0.00044
NM_001365951.3(KIF1B):c.*2019C>T rs185749715 0.00037
NM_001365951.3(KIF1B):c.2604C>T (p.Asp868=) rs145846362 0.00031
NM_001365951.3(KIF1B):c.*1117C>T rs182518399 0.00022
NM_001365951.3(KIF1B):c.3636G>A (p.Pro1212=) rs140229905 0.00019
NM_001365951.3(KIF1B):c.*4238G>T rs544754092 0.00017
NM_001365951.3(KIF1B):c.1955C>T (p.Thr652Ile) rs142881321 0.00017
NM_001365951.3(KIF1B):c.4967G>A (p.Arg1656Gln) rs373439616 0.00017
NM_001365951.3(KIF1B):c.4338A>G (p.Leu1446=) rs143112560 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.*3418C>T rs559140260 0.00008
NM_001365951.3(KIF1B):c.5409-15G>A rs371830018 0.00007
NM_001365951.3(KIF1B):c.*4041C>G rs539967376 0.00006
NM_001365951.3(KIF1B):c.*1715G>T rs755083691 0.00004
NM_001365951.3(KIF1B):c.4282G>A (p.Gly1428Ser) rs754234374 0.00004
NM_001365951.3(KIF1B):c.-127G>A rs528568887 0.00001
NM_001365951.3(KIF1B):c.4155G>T (p.Leu1385Phe) rs760253167 0.00001
NM_001365951.3(KIF1B):c.4544G>A (p.Arg1515His) rs375130478 0.00001
NM_001365951.3(KIF1B):c.*3352G>C rs567769024
NM_001365951.3(KIF1B):c.*375A>G rs554239975
NM_001365951.3(KIF1B):c.*4127dup rs548680591
NM_001365951.3(KIF1B):c.*4279dup rs531640427
NM_001365951.3(KIF1B):c.168C>T (p.Tyr56=) rs530566864
NM_001365951.3(KIF1B):c.184-6_184-5del rs138324955
NM_001365951.3(KIF1B):c.4977T>C (p.Ser1659=) rs778240671

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