ClinVar Miner

List of variants in gene TBC1D24 reported as uncertain significance by Ambry Genetics

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Total variants: 19
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HGVS dbSNP
NM_001199107.2(TBC1D24):c.*1C>T
NM_001199107.2(TBC1D24):c.1171C>G (p.Pro391Ala) rs1435411888
NM_001199107.2(TBC1D24):c.1327G>A (p.Glu443Lys) rs141399869
NM_001199107.2(TBC1D24):c.1570C>T (p.Arg524Trp) rs78644690
NM_001199107.2(TBC1D24):c.1642G>A (p.Val548Met) rs201649140
NM_001199107.2(TBC1D24):c.169C>T (p.Arg57Cys) rs202162520
NM_001199107.2(TBC1D24):c.229_240ATCGTGGGCAAG[1] (p.77_80IVGK[1]) rs761918906
NM_001199107.2(TBC1D24):c.242T>C (p.Ile81Thr) rs1347306529
NM_001199107.2(TBC1D24):c.343C>T (p.Arg115Cys) rs372531999
NM_001199107.2(TBC1D24):c.381C>A (p.Asp127Glu) rs1376844321
NM_001199107.2(TBC1D24):c.457G>A (p.Glu153Lys) rs376712059
NM_001199107.2(TBC1D24):c.470G>A (p.Arg157His) rs1301489148
NM_001199107.2(TBC1D24):c.641G>A (p.Arg214His) rs200324356
NM_001199107.2(TBC1D24):c.680G>T (p.Arg227Leu) rs756181906
NM_001199107.2(TBC1D24):c.829G>A (p.Ala277Thr) rs754019727
NM_001199107.2(TBC1D24):c.845C>G (p.Pro282Arg) rs747538224
NM_001199107.2(TBC1D24):c.871G>A (p.Ala291Thr) rs375307187
NM_001199107.2(TBC1D24):c.878G>A (p.Arg293His) rs199700840
NM_001199107.2(TBC1D24):c.965G>A (p.Ser322Asn) rs1567412410

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