ClinVar Miner

List of variants in gene TBC1D24 reported as likely benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 105
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HGVS dbSNP
NM_001199107.2(TBC1D24):c.1008T>C (p.His336=)
NM_001199107.2(TBC1D24):c.1020C>T (p.Phe340=)
NM_001199107.2(TBC1D24):c.1026G>A (p.Ser342=) rs370244846
NM_001199107.2(TBC1D24):c.102A>G (p.Glu34=) rs1178639246
NM_001199107.2(TBC1D24):c.1038C>T (p.Ser346=) rs377697825
NM_001199107.2(TBC1D24):c.1071C>T (p.Val357=) rs760897479
NM_001199107.2(TBC1D24):c.1110C>T (p.Phe370=) rs1555501404
NM_001199107.2(TBC1D24):c.1119G>T (p.Leu373=)
NM_001199107.2(TBC1D24):c.1125C>T (p.His375=) rs749163517
NM_001199107.2(TBC1D24):c.1137G>A (p.Leu379=) rs1243475474
NM_001199107.2(TBC1D24):c.1142+7C>A
NM_001199107.2(TBC1D24):c.1143-5G>A
NM_001199107.2(TBC1D24):c.1143-5G>T rs754105574
NM_001199107.2(TBC1D24):c.117G>A (p.Ala39=)
NM_001199107.2(TBC1D24):c.1196C>T (p.Thr399Met) rs61731477
NM_001199107.2(TBC1D24):c.1207-7C>T
NM_001199107.2(TBC1D24):c.1209G>A (p.Val403=)
NM_001199107.2(TBC1D24):c.1260C>A (p.Gly420=)
NM_001199107.2(TBC1D24):c.1278G>A (p.Gly426=) rs377748101
NM_001199107.2(TBC1D24):c.1281C>T (p.Thr427=) rs200089341
NM_001199107.2(TBC1D24):c.1302+9G>A
NM_001199107.2(TBC1D24):c.1327G>A (p.Glu443Lys) rs141399869
NM_001199107.2(TBC1D24):c.1341C>A (p.Ile447=) rs372317366
NM_001199107.2(TBC1D24):c.1341C>T (p.Ile447=) rs372317366
NM_001199107.2(TBC1D24):c.1350C>T (p.Pro450=) rs375320196
NM_001199107.2(TBC1D24):c.1353G>A (p.Glu451=) rs1231827471
NM_001199107.2(TBC1D24):c.1367C>T (p.Pro456Leu) rs200641000
NM_001199107.2(TBC1D24):c.1383C>T (p.Ala461=)
NM_001199107.2(TBC1D24):c.1392C>T (p.Thr464=) rs199865687
NM_001199107.2(TBC1D24):c.1410C>A (p.Ser470=)
NM_001199107.2(TBC1D24):c.1410C>G (p.Ser470=)
NM_001199107.2(TBC1D24):c.1410C>T (p.Ser470=) rs553497128
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.1437C>T (p.Leu479=)
NM_001199107.2(TBC1D24):c.1446C>T (p.Phe482=)
NM_001199107.2(TBC1D24):c.144C>T (p.His48=)
NM_001199107.2(TBC1D24):c.1467C>T (p.Asn489=) rs779963634
NM_001199107.2(TBC1D24):c.1482C>T (p.Thr494=)
NM_001199107.2(TBC1D24):c.1500G>C (p.Ala500=)
NM_001199107.2(TBC1D24):c.1503G>A (p.Gly501=) rs368735897
NM_001199107.2(TBC1D24):c.1521C>T (p.Ile507=)
NM_001199107.2(TBC1D24):c.1525+7G>A rs1041091510
NM_001199107.2(TBC1D24):c.1548C>T (p.Leu516=) rs1555501692
NM_001199107.2(TBC1D24):c.1570C>T (p.Arg524Trp) rs78644690
NM_001199107.2(TBC1D24):c.1581A>G (p.Thr527=)
NM_001199107.2(TBC1D24):c.1590C>T (p.Cys530=) rs1060502501
NM_001199107.2(TBC1D24):c.1620C>T (p.Ser540=) rs781723084
NM_001199107.2(TBC1D24):c.1642G>A (p.Val548Met) rs201649140
NM_001199107.2(TBC1D24):c.178C>T (p.Arg60Trp) rs373914077
NM_001199107.2(TBC1D24):c.192C>T (p.Cys64=) rs878854271
NM_001199107.2(TBC1D24):c.210C>T (p.Asp70=) rs373872223
NM_001199107.2(TBC1D24):c.213C>T (p.Ala71=) rs778212970
NM_001199107.2(TBC1D24):c.225C>T (p.Ser75=) rs201220026
NM_001199107.2(TBC1D24):c.22T>C (p.Cys8Arg) rs77585883
NM_001199107.2(TBC1D24):c.243C>T (p.Ile81=) rs745405784
NM_001199107.2(TBC1D24):c.264C>T (p.Ser88=)
NM_001199107.2(TBC1D24):c.273G>A (p.Pro91=)
NM_001199107.2(TBC1D24):c.27C>T (p.Phe9=) rs759193465
NM_001199107.2(TBC1D24):c.297G>A (p.Thr99=) rs767766165
NM_001199107.2(TBC1D24):c.327C>T (p.Arg109=) rs754551693
NM_001199107.2(TBC1D24):c.333G>A (p.Glu111=) rs749237671
NM_001199107.2(TBC1D24):c.344G>A (p.Arg115His) rs201174513
NM_001199107.2(TBC1D24):c.378C>T (p.Pro126=) rs765624033
NM_001199107.2(TBC1D24):c.384C>T (p.Ile128=)
NM_001199107.2(TBC1D24):c.438C>T (p.Ile146=)
NM_001199107.2(TBC1D24):c.447C>T (p.Ala149=) rs755794991
NM_001199107.2(TBC1D24):c.456C>T (p.Phe152=)
NM_001199107.2(TBC1D24):c.465C>T (p.Ala155=) rs1596968205
NM_001199107.2(TBC1D24):c.48C>T (p.Asp16=) rs555276293
NM_001199107.2(TBC1D24):c.492C>G (p.Pro164=) rs369172908
NM_001199107.2(TBC1D24):c.493G>A (p.Gly165Ser) rs200926225
NM_001199107.2(TBC1D24):c.495C>G (p.Gly165=)
NM_001199107.2(TBC1D24):c.507C>T (p.Ile169=) rs529104933
NM_001199107.2(TBC1D24):c.519C>T (p.Phe173=) rs763534843
NM_001199107.2(TBC1D24):c.534G>A (p.Ser178=) rs144714321
NM_001199107.2(TBC1D24):c.546G>A (p.Thr182=) rs182825122
NM_001199107.2(TBC1D24):c.630G>A (p.Ala210=) rs776459372
NM_001199107.2(TBC1D24):c.648G>C (p.Leu216=) rs571126287
NM_001199107.2(TBC1D24):c.64C>T (p.Leu22=)
NM_001199107.2(TBC1D24):c.651T>C (p.Phe217=) rs750100459
NM_001199107.2(TBC1D24):c.690C>T (p.Asp230=) rs749531792
NM_001199107.2(TBC1D24):c.702G>A (p.Val234=) rs188739853
NM_001199107.2(TBC1D24):c.702G>C (p.Val234=) rs188739853
NM_001199107.2(TBC1D24):c.726C>T (p.Arg242=) rs772786813
NM_001199107.2(TBC1D24):c.732G>A (p.Ala244=)
NM_001199107.2(TBC1D24):c.785C>T (p.Ser262Leu) rs201060500
NM_001199107.2(TBC1D24):c.786G>A (p.Ser262=)
NM_001199107.2(TBC1D24):c.792C>T (p.Ser264=) rs769290045
NM_001199107.2(TBC1D24):c.813G>A (p.Thr271=) rs527719763
NM_001199107.2(TBC1D24):c.816C>T (p.Phe272=)
NM_001199107.2(TBC1D24):c.828C>T (p.Ile276=)
NM_001199107.2(TBC1D24):c.855G>T (p.Leu285=)
NM_001199107.2(TBC1D24):c.864A>G (p.Lys288=) rs777237669
NM_001199107.2(TBC1D24):c.870C>T (p.Phe290=)
NM_001199107.2(TBC1D24):c.90T>C (p.Thr30=) rs575173753
NM_001199107.2(TBC1D24):c.94C>T (p.Leu32=)
NM_001199107.2(TBC1D24):c.951C>T (p.Thr317=) rs766745103
NM_001199107.2(TBC1D24):c.965+10C>T rs756687194
NM_001199107.2(TBC1D24):c.965+7C>T
NM_001199107.2(TBC1D24):c.965+8G>A rs372247100
NM_001199107.2(TBC1D24):c.969G>A (p.Val323=) rs1054785696
NM_001199107.2(TBC1D24):c.983+7C>T rs778459711
NM_001199107.2(TBC1D24):c.984-5C>T
NM_001199107.2(TBC1D24):c.984-7C>T

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