ClinVar Miner

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

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Gene type:
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Total variants: 38
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HGVS dbSNP
NM_001365951.3(KIF1B):c.*1238G>A
NM_001365951.3(KIF1B):c.*3352G>C
NM_001365951.3(KIF1B):c.*4041C>G
NM_001365951.3(KIF1B):c.*4238G>T
NM_001365951.3(KIF1B):c.1435-15C>T
NM_001365951.3(KIF1B):c.4282G>A (p.Gly1428Ser)
NM_001365951.3(KIF1B):c.429+7A>G
NM_001365951.3(KIF1B):c.4338A>G (p.Leu1446=) rs143112560
NM_001365951.3(KIF1B):c.4544G>A (p.Arg1515His)
NM_001365951.3(KIF1B):c.4967G>A (p.Arg1656Gln)
NM_001365951.3(KIF1B):c.5409-15G>A
NM_015074.3(KIF1B):c.*1117C>T rs182518399
NM_015074.3(KIF1B):c.*1715G>T rs755083691
NM_015074.3(KIF1B):c.*2019C>T rs185749715
NM_015074.3(KIF1B):c.*3035G>A rs41301987
NM_015074.3(KIF1B):c.*3418C>T rs559140260
NM_015074.3(KIF1B):c.*375A>G rs554239975
NM_015074.3(KIF1B):c.*3930C>T rs549049444
NM_015074.3(KIF1B):c.*4113C>T rs192312673
NM_015074.3(KIF1B):c.*4127dup rs548680591
NM_015074.3(KIF1B):c.*4279dup rs531640427
NM_015074.3(KIF1B):c.*4325G>A rs141688466
NM_015074.3(KIF1B):c.-127G>A rs528568887
NM_015074.3(KIF1B):c.168C>T (p.Tyr56=) rs530566864
NM_015074.3(KIF1B):c.1817C>T (p.Thr606Ile) rs142881321
NM_015074.3(KIF1B):c.184-6_184-5del rs138324955
NM_015074.3(KIF1B):c.2455A>C (p.Ser819Arg) rs140015591
NM_015074.3(KIF1B):c.2466C>T (p.Asp822=) rs145846362
NM_015074.3(KIF1B):c.3285-15del rs3215996
NM_015074.3(KIF1B):c.3498G>A (p.Pro1166=) rs140229905
NM_015074.3(KIF1B):c.3507G>A (p.Pro1169=) rs147318592
NM_015074.3(KIF1B):c.4017G>T (p.Leu1339Phe) rs760253167
NM_015074.3(KIF1B):c.4682G>A (p.Cys1561Tyr) rs145969842
NM_015074.3(KIF1B):c.4839T>C (p.Ser1613=) rs778240671
NM_015074.3(KIF1B):c.4882G>A (p.Glu1628Lys) rs143669846
NM_015074.3(KIF1B):c.608+8dup rs139613776
NM_183416.4(KIF1B):c.-260C>T rs149705989
NM_183416.4(KIF1B):c.-26_-25TA[7] rs34063243

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