ClinVar Miner

List of variants in gene KIF1B reported as uncertain significance for adrenal gland neoplasm

Included ClinVar conditions (53):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_001365951.3(KIF1B):c.315T>C (p.Tyr105=) rs144889528 0.00009
NM_001365951.3(KIF1B):c.215G>A (p.Arg72His) rs761343609 0.00008
NM_001365951.3(KIF1B):c.*3644dup rs775451005 0.00007
NM_001365951.3(KIF1B):c.*2032T>A rs190108168 0.00005
NM_001365951.3(KIF1B):c.2115+6545C>A rs1299989581 0.00004
NM_001365951.3(KIF1B):c.2611G>A (p.Glu871Lys) rs763122049 0.00004
NM_001365951.3(KIF1B):c.1705A>G (p.Ile569Val) rs374848403 0.00003
NM_001365951.3(KIF1B):c.5203A>G (p.Ser1735Gly) rs775692548 0.00003
NM_001365951.3(KIF1B):c.3434G>A (p.Arg1145His) rs373663596 0.00002
NM_001365951.3(KIF1B):c.5225G>A (p.Arg1742His) rs768058092 0.00002
NM_001365951.3(KIF1B):c.*1104C>T rs886044995 0.00001
NM_001365951.3(KIF1B):c.1038-5del rs886044976 0.00001
NM_001365951.3(KIF1B):c.2115+6476T>C rs764466176 0.00001
NM_001365951.3(KIF1B):c.2174C>T (p.Ala725Val) rs773852256 0.00001
NM_001365951.3(KIF1B):c.445A>G (p.Ile149Val) rs1051917954 0.00001
NM_001365951.3(KIF1B):c.4601T>G (p.Leu1534Arg) rs1011009249 0.00001
NM_001365951.3(KIF1B):c.5176C>T (p.Arg1726Cys) rs754479325 0.00001
NM_001365951.3(KIF1B):c.*1363dup rs567435289
NM_001365951.3(KIF1B):c.*249CA[13] rs111663673
NM_001365951.3(KIF1B):c.*249CA[14] rs111663673
NM_001365951.3(KIF1B):c.*249CA[17] rs111663673
NM_001365951.3(KIF1B):c.*249CA[18] rs111663673
NM_001365951.3(KIF1B):c.*249CA[19] rs111663673
NM_001365951.3(KIF1B):c.*281_*282dup rs886044986
NM_001365951.3(KIF1B):c.*281_*286del rs886044990
NM_001365951.3(KIF1B):c.*2978dup rs145348144
NM_001365951.3(KIF1B):c.*454CT[1] rs886044993
NM_001365951.3(KIF1B):c.*4664_*4665insG rs571589510
NM_001365951.3(KIF1B):c.2115+6012C>G
NM_001365951.3(KIF1B):c.2115+7115C>A
NM_001365951.3(KIF1B):c.2115+7270G>A
NM_001365951.3(KIF1B):c.2115+7343G>A
NM_001365951.3(KIF1B):c.3163G>T (p.Gly1055Cys) rs2102315795
NM_001365951.3(KIF1B):c.3290A>G (p.Lys1097Arg)
NM_001365951.3(KIF1B):c.4321A>T (p.Ile1441Phe)
NM_001365951.3(KIF1B):c.5300C>G (p.Thr1767Ser)
NM_001365951.3(KIF1B):c.883-10_883-7del rs886044975

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