ClinVar Miner

List of variants in gene TBC1D24 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 40
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HGVS dbSNP
NM_001199107.1(TBC1D24):c.1022G>A (p.Arg341His) rs754727069
NM_001199107.1(TBC1D24):c.1028A>C (p.Glu343Ala) rs188124777
NM_001199107.1(TBC1D24):c.1126G>C (p.Gly376Arg) rs796053408
NM_001199107.1(TBC1D24):c.116C>A (p.Ala39Glu) rs773916549
NM_001199107.1(TBC1D24):c.1196C>T (p.Thr399Met) rs61731477
NM_001199107.1(TBC1D24):c.1207-16C>G rs201618854
NM_001199107.1(TBC1D24):c.1207-6C>G rs749626631
NM_001199107.1(TBC1D24):c.1253T>C (p.Phe418Ser) rs776176742
NM_001199107.1(TBC1D24):c.1303-5C>G rs1468286638
NM_001199107.1(TBC1D24):c.1327G>A (p.Glu443Lys) rs141399869
NM_001199107.1(TBC1D24):c.1367C>T (p.Pro456Leu) rs200641000
NM_001199107.1(TBC1D24):c.1453G>A (p.Ala485Thr) rs774586263
NM_001199107.1(TBC1D24):c.1457G>A (p.Arg486His) rs796053405
NM_001199107.1(TBC1D24):c.1510G>A (p.Asp504Asn) rs767925237
NM_001199107.1(TBC1D24):c.1526G>T (p.Gly509Val) rs796053406
NM_001199107.1(TBC1D24):c.1590C>G (p.Cys530Trp) rs1060502501
NM_001199107.1(TBC1D24):c.1633A>G (p.Ile545Val) rs773874436
NM_001199107.1(TBC1D24):c.1642G>A (p.Val548Met) rs201649140
NM_001199107.1(TBC1D24):c.169C>T (p.Arg57Cys) rs202162520
NM_001199107.1(TBC1D24):c.170G>A (p.Arg57His) rs370100394
NM_001199107.1(TBC1D24):c.178C>T (p.Arg60Trp) rs373914077
NM_001199107.1(TBC1D24):c.20A>G (p.Asn7Ser) rs765897138
NM_001199107.1(TBC1D24):c.340G>A (p.Val114Met) rs368575199
NM_001199107.1(TBC1D24):c.343C>T (p.Arg115Cys) rs372531999
NM_001199107.1(TBC1D24):c.344G>A (p.Arg115His) rs201174513
NM_001199107.1(TBC1D24):c.379G>A (p.Asp127Asn) rs750962753
NM_001199107.1(TBC1D24):c.578C>T (p.Ala193Val) rs750266156
NM_001199107.1(TBC1D24):c.605C>T (p.Ser202Leu) rs796053400
NM_001199107.1(TBC1D24):c.676G>A (p.Ala226Thr) rs796053401
NM_001199107.1(TBC1D24):c.776C>T (p.Pro259Leu) rs779398267
NM_001199107.1(TBC1D24):c.816C>A (p.Phe272Leu) rs796053402
NM_001199107.1(TBC1D24):c.820A>G (p.Arg274Gly) rs760591932
NM_001199107.1(TBC1D24):c.829G>T (p.Ala277Ser) rs754019727
NM_001199107.1(TBC1D24):c.871G>A (p.Ala291Thr) rs375307187
NM_001199107.1(TBC1D24):c.878G>A (p.Arg293His) rs199700840
NM_001199107.1(TBC1D24):c.890G>A (p.Arg297His) rs760666914
NM_001199107.1(TBC1D24):c.920A>C (p.Asn307Thr) rs761934676
NM_001199107.1(TBC1D24):c.983G>T (p.Arg328Met) rs796053404
NM_020705.2(TBC1D24):c.1472T>C (p.Met491Thr) rs367710709
NM_020705.2(TBC1D24):c.793G>A (p.Val265Met) rs772768393

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