ClinVar Miner

List of variants in gene TBC1D24 reported as benign for not provided

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_001199107.2(TBC1D24):c.*188C>T rs62040717 0.06494
NM_001199107.2(TBC1D24):c.*56C>T rs76267944 0.03630
NM_001199107.2(TBC1D24):c.-116+73C>T rs534611598 0.02428
NM_001199107.2(TBC1D24):c.1440G>A (p.Ser480=) rs12373107 0.02286
NM_001199107.2(TBC1D24):c.1302+32C>T rs9938969 0.02259
NM_001199107.2(TBC1D24):c.1302+138C>T rs9939054 0.02136
NM_001199107.2(TBC1D24):c.1303-157T>C rs9931334 0.02123
NM_001199107.2(TBC1D24):c.1302+158T>C rs9931326 0.02120
NM_001199107.2(TBC1D24):c.1302+134C>T rs9939052 0.02116
NM_001199107.2(TBC1D24):c.1526-24G>A rs4074464 0.02079
NM_001199107.2(TBC1D24):c.1509C>T (p.Ser503=) rs189089167 0.01110
NM_001199107.2(TBC1D24):c.885C>G (p.Phe295Leu) rs72768728 0.00609
NM_001199107.2(TBC1D24):c.1302+38C>T rs9938971 0.00481
NM_001199107.2(TBC1D24):c.1500G>A (p.Ala500=) rs201059992 0.00334
NM_001199107.2(TBC1D24):c.1326C>T (p.Tyr442=) rs184639841 0.00324
NM_001199107.2(TBC1D24):c.1196C>T (p.Thr399Met) rs61731477 0.00306
NM_001199107.2(TBC1D24):c.1427C>A (p.Ala476Asp) rs202216463 0.00304
NM_001199107.2(TBC1D24):c.663C>T (p.Pro221=) rs148670169 0.00019
NM_001199107.2(TBC1D24):c.414G>A (p.Val138=) rs1015174831 0.00001
NM_001199107.2(TBC1D24):c.*36G>T rs73490289
NM_020705.2:c.+1C>T

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