ClinVar Miner

List of variants in gene TBC1D24 reported as uncertain significance for not provided

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Total variants: 64
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HGVS dbSNP
NM_001199107.2(TBC1D24):c.-4C>T rs202124579
NM_001199107.2(TBC1D24):c.1015A>G (p.Asn339Asp) rs574768683
NM_001199107.2(TBC1D24):c.1022G>A (p.Arg341His) rs754727069
NM_001199107.2(TBC1D24):c.1028A>C (p.Glu343Ala) rs188124777
NM_001199107.2(TBC1D24):c.1038C>T (p.Ser346=) rs377697825
NM_001199107.2(TBC1D24):c.1039G>A (p.Val347Met) rs371031447
NM_001199107.2(TBC1D24):c.1072C>A (p.Pro358Thr)
NM_001199107.2(TBC1D24):c.1125C>T (p.His375=) rs749163517
NM_001199107.2(TBC1D24):c.1126G>C (p.Gly376Arg) rs796053408
NM_001199107.2(TBC1D24):c.1137G>A (p.Leu379=) rs1243475474
NM_001199107.2(TBC1D24):c.1207-16C>G rs201618854
NM_001199107.2(TBC1D24):c.1207-6C>G rs749626631
NM_001199107.2(TBC1D24):c.1253T>C (p.Phe418Ser) rs776176742
NM_001199107.2(TBC1D24):c.1303-5C>G rs1468286638
NM_001199107.2(TBC1D24):c.1327G>A (p.Glu443Lys) rs141399869
NM_001199107.2(TBC1D24):c.1367C>A (p.Pro456Gln) rs200641000
NM_001199107.2(TBC1D24):c.1367C>T (p.Pro456Leu) rs200641000
NM_001199107.2(TBC1D24):c.13G>C (p.Gly5Arg) rs772570554
NM_001199107.2(TBC1D24):c.1411G>A (p.Ala471Thr) rs377448015
NM_001199107.2(TBC1D24):c.1425C>T (p.Pro475=) rs370869383
NM_001199107.2(TBC1D24):c.1453G>A (p.Ala485Thr) rs774586263
NM_001199107.2(TBC1D24):c.1457G>A (p.Arg486His) rs796053405
NM_001199107.2(TBC1D24):c.1473C>G (p.Pro491=) rs370427146
NM_001199107.2(TBC1D24):c.1490T>C (p.Met497Thr) rs367710709
NM_001199107.2(TBC1D24):c.1510G>A (p.Asp504Asn) rs767925237
NM_001199107.2(TBC1D24):c.1525+6C>T rs758013935
NM_001199107.2(TBC1D24):c.1525G>A (p.Gly509Arg) rs749994791
NM_001199107.2(TBC1D24):c.1526G>T (p.Gly509Val) rs796053406
NM_001199107.2(TBC1D24):c.1544C>T (p.Ala515Val) rs267607105
NM_001199107.2(TBC1D24):c.1554C>T (p.Ile518=)
NM_001199107.2(TBC1D24):c.1590C>G (p.Cys530Trp) rs1060502501
NM_001199107.2(TBC1D24):c.1606del (p.Gln536fs) rs1567414972
NM_001199107.2(TBC1D24):c.1620C>T (p.Ser540=) rs781723084
NM_001199107.2(TBC1D24):c.1633A>G (p.Ile545Val) rs773874436
NM_001199107.2(TBC1D24):c.1642G>A (p.Val548Met) rs201649140
NM_001199107.2(TBC1D24):c.1674C>T (p.Thr558=) rs750341354
NM_001199107.2(TBC1D24):c.1675C>T (p.Gln559Ter) rs1253505916
NM_001199107.2(TBC1D24):c.169C>T (p.Arg57Cys) rs202162520
NM_001199107.2(TBC1D24):c.170G>A (p.Arg57His) rs370100394
NM_001199107.2(TBC1D24):c.178C>T (p.Arg60Trp) rs373914077
NM_001199107.2(TBC1D24):c.179G>A (p.Arg60Gln) rs200226466
NM_001199107.2(TBC1D24):c.20A>G (p.Asn7Ser) rs765897138
NM_001199107.2(TBC1D24):c.285C>T (p.Phe95=) rs774354974
NM_001199107.2(TBC1D24):c.340G>A (p.Val114Met) rs368575199
NM_001199107.2(TBC1D24):c.343C>T (p.Arg115Cys) rs372531999
NM_001199107.2(TBC1D24):c.344G>A (p.Arg115His) rs201174513
NM_001199107.2(TBC1D24):c.379G>A (p.Asp127Asn) rs750962753
NM_001199107.2(TBC1D24):c.389_391del (p.Phe130del) rs1418389627
NM_001199107.2(TBC1D24):c.578C>T (p.Ala193Val) rs750266156
NM_001199107.2(TBC1D24):c.605C>T (p.Ser202Leu) rs796053400
NM_001199107.2(TBC1D24):c.606G>A (p.Ser202=)
NM_001199107.2(TBC1D24):c.676G>A (p.Ala226Thr) rs796053401
NM_001199107.2(TBC1D24):c.702G>A (p.Val234=) rs188739853
NM_001199107.2(TBC1D24):c.776C>T (p.Pro259Leu) rs779398267
NM_001199107.2(TBC1D24):c.793G>A (p.Val265Met) rs772768393
NM_001199107.2(TBC1D24):c.816C>A (p.Phe272Leu) rs796053402
NM_001199107.2(TBC1D24):c.820A>G (p.Arg274Gly) rs760591932
NM_001199107.2(TBC1D24):c.829G>T (p.Ala277Ser) rs754019727
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.890G>A (p.Arg297His) rs760666914
NM_001199107.2(TBC1D24):c.920A>C (p.Asn307Thr) rs761934676
NM_001199107.2(TBC1D24):c.972A>C (p.Ser324=) rs886043654
NM_001199107.2(TBC1D24):c.983G>T (p.Arg328Met) rs796053404

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