ClinVar Miner

List of variants in gene TBC1D24 reported as benign for Myoclonic epilepsy, familial infantile

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Total variants: 28
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HGVS dbSNP
NM_001199107.2(TBC1D24):c.*1160G>A rs7201970
NM_001199107.2(TBC1D24):c.*1575C>T rs4786286
NM_001199107.2(TBC1D24):c.*1659G>A rs115543208
NM_001199107.2(TBC1D24):c.*1691G>A rs77858505
NM_001199107.2(TBC1D24):c.*1814G>C rs28668740
NM_001199107.2(TBC1D24):c.*188C>T rs62040717
NM_001199107.2(TBC1D24):c.*2395A>G rs11543247
NM_001199107.2(TBC1D24):c.*2529A>T rs565226115
NM_001199107.2(TBC1D24):c.*2598G>C rs13336179
NM_001199107.2(TBC1D24):c.*2625dup rs35944492
NM_001199107.2(TBC1D24):c.*2910A>T rs4786287
NM_001199107.2(TBC1D24):c.*3408C>T rs9935554
NM_001199107.2(TBC1D24):c.*36G>T rs73490289
NM_001199107.2(TBC1D24):c.*3712C>T rs185371000
NM_001199107.2(TBC1D24):c.*3715C>T rs55778555
NM_001199107.2(TBC1D24):c.*385C>T
NM_001199107.2(TBC1D24):c.*389C>A rs189378766
NM_001199107.2(TBC1D24):c.*4067C>T rs74003014
NM_001199107.2(TBC1D24):c.*4120T>C
NM_001199107.2(TBC1D24):c.*4479C>T rs1135527
NM_001199107.2(TBC1D24):c.*56C>T rs76267944
NM_001199107.2(TBC1D24):c.*732A>G rs4075481
NM_001199107.2(TBC1D24):c.*836C>T rs4075480
NM_001199107.2(TBC1D24):c.-31T>C rs13339105
NM_001199107.2(TBC1D24):c.1143-6C>T rs73490287
NM_001199107.2(TBC1D24):c.1440G>A (p.Ser480=) rs12373107
NM_001199107.2(TBC1D24):c.1509C>T (p.Ser503=) rs189089167
NM_001199107.2(TBC1D24):c.207T>C (p.Pro69=) rs13339237

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