ClinVar Miner

List of variants in gene KIF1B reported as benign for embryonal neoplasm

Included ClinVar conditions (54):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_001365951.3(KIF1B):c.*2042C>T rs1536262 0.55000
NM_015074.3(KIF1B):c.*5019T>C rs3748581 0.53815
NM_001365951.3(KIF1B):c.*3911A>G rs1138791 0.35950
NM_001365951.3(KIF1B):c.*2247G>A rs1002076 0.32846
NM_001365951.3(KIF1B):c.1777+10C>T rs3753037 0.26503
NM_001365951.3(KIF1B):c.285C>G (p.Ala95=) rs12402052 0.24010
NM_001365951.3(KIF1B):c.5301C>A (p.Thr1767=) rs11121552 0.23676
NM_001365951.3(KIF1B):c.*1159G>A rs4240913 0.09825
NM_001365951.3(KIF1B):c.*1133C>T rs4240912 0.09823
NM_001365951.3(KIF1B):c.4299A>G (p.Pro1433=) rs12125492 0.08850
NM_001365951.3(KIF1B):c.*2661A>T rs6694522 0.03958
NM_001365951.3(KIF1B):c.*1361A>T rs2847347 0.03872
NM_001365951.3(KIF1B):c.*4392A>G rs72867441 0.03534
NM_001365951.3(KIF1B):c.4946+9C>T rs72867431 0.03521
NM_001365951.3(KIF1B):c.1365G>A (p.Thr455=) rs17034660 0.03490
NM_001365951.3(KIF1B):c.3398A>G (p.Tyr1133Cys) rs2297881 0.03425
NM_001365951.3(KIF1B):c.*3154A>G rs41310365 0.03073
NM_001365951.3(KIF1B):c.-80+1G>T rs140240544 0.02890
NM_001365951.3(KIF1B):c.*1118G>A rs7544928 0.02869
NM_001365951.3(KIF1B):c.-136C>T rs181820595 0.02054
NM_001365951.3(KIF1B):c.*2698G>A rs115172954 0.01866
NM_001365951.3(KIF1B):c.363+6A>C rs114084418 0.01751
NM_001365951.3(KIF1B):c.*2869C>T rs3748580 0.01676
NM_001365951.3(KIF1B):c.5432C>T (p.Pro1811Leu) rs61999305 0.01293
NM_001365951.3(KIF1B):c.4798G>A (p.Val1600Met) rs77172218 0.01096
NM_001365951.3(KIF1B):c.*4267A>G rs77474900 0.01073
NM_001365951.3(KIF1B):c.*712G>A rs146717943 0.01069
NM_001365951.3(KIF1B):c.4086T>C (p.Asp1362=) rs116089798 0.01068
NM_001365951.3(KIF1B):c.*279C>T rs78490707 0.00800
NM_001365951.3(KIF1B):c.3864+6A>C rs114266141 0.00716
NM_001365951.3(KIF1B):c.4055+6A>G rs76519832 0.00707
NM_001365951.3(KIF1B):c.*4894T>C rs77885116 0.00664
NM_001365951.3(KIF1B):c.*1503C>T rs116167243 0.00570
NM_001365951.3(KIF1B):c.*3742T>C rs78868210 0.00563
NM_001365951.3(KIF1B):c.*3341C>T rs139210251 0.00535
NM_001365951.3(KIF1B):c.5250A>G (p.Ala1750=) rs75413741 0.00415
NM_001365951.3(KIF1B):c.*2732G>C rs190725532 0.00331
NM_001365951.3(KIF1B):c.2330A>G (p.Asn777Ser) rs117525287 0.00228
NM_001365951.3(KIF1B):c.*2895G>A rs184232081 0.00197
NM_001365951.3(KIF1B):c.*2T>C rs148690591 0.00185
NM_001365951.3(KIF1B):c.4596C>T (p.Pro1532=) rs147066476 0.00150
NM_001365951.3(KIF1B):c.*3690C>A rs540616562 0.00140
NM_001365951.3(KIF1B):c.*4958G>A rs150497684 0.00133
NM_001365951.3(KIF1B):c.3259+9A>G rs149566646 0.00118
NM_001365951.3(KIF1B):c.3885A>C (p.Thr1295=) rs139159572 0.00092
NM_001365951.3(KIF1B):c.*1986C>G rs557129908 0.00054
NM_001365951.3(KIF1B):c.*3948G>A rs553404052 0.00026
NM_001365951.3(KIF1B):c.*3988G>A rs571451087 0.00014
NM_001365951.3(KIF1B):c.3423-15A>T rs200470260 0.00005
NM_001365951.3(KIF1B):c.2245T>C (p.Trp749Arg) rs551543997 0.00004
NM_001365951.3(KIF1B):c.*2012C>T rs181454124 0.00003
NM_001365951.3(KIF1B):c.*2321A>G rs567547345 0.00003
NM_001365951.3(KIF1B):c.*249CA[15] rs111663673
NM_001365951.3(KIF1B):c.*2740C>A rs144047666
NM_001365951.3(KIF1B):c.*3857G>A rs536529721

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