ClinVar Miner

List of variants in gene TBC1D24 reported as likely benign for not specified

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Gene type:
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Total variants: 80
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HGVS dbSNP
NM_001199107.2(TBC1D24):c.*2G>A rs780054979
NM_001199107.2(TBC1D24):c.-115-17T>C rs891836551
NM_001199107.2(TBC1D24):c.-116+13G>C rs1057522733
NM_001199107.2(TBC1D24):c.-116+3G>T rs998707315
NM_001199107.2(TBC1D24):c.-119G>C rs1230756942
NM_001199107.2(TBC1D24):c.-121G>A rs1057521709
NM_001199107.2(TBC1D24):c.-134G>C rs1346593000
NM_001199107.2(TBC1D24):c.-137_-135GAG[1] rs1010877040
NM_001199107.2(TBC1D24):c.-15G>A rs201377976
NM_001199107.2(TBC1D24):c.-15G>C rs201377976
NM_001199107.2(TBC1D24):c.-30C>T rs371415659
NM_001199107.2(TBC1D24):c.-7C>T rs199852092
NM_001199107.2(TBC1D24):c.-99C>G rs540861763
NM_001199107.2(TBC1D24):c.1002C>T (p.Ala334=) rs184389316
NM_001199107.2(TBC1D24):c.1026G>A (p.Ser342=) rs370244846
NM_001199107.2(TBC1D24):c.1038C>T (p.Ser346=) rs377697825
NM_001199107.2(TBC1D24):c.1125C>T (p.His375=) rs749163517
NM_001199107.2(TBC1D24):c.1142+14G>A rs745904419
NM_001199107.2(TBC1D24):c.1143-6C>T rs73490287
NM_001199107.2(TBC1D24):c.1206+13C>T rs376162122
NM_001199107.2(TBC1D24):c.1302+14A>C rs528462687
NM_001199107.2(TBC1D24):c.1305G>C (p.Leu435=) rs774088745
NM_001199107.2(TBC1D24):c.1326C>T (p.Tyr442=) rs184639841
NM_001199107.2(TBC1D24):c.1425C>T (p.Pro475=) rs370869383
NM_001199107.2(TBC1D24):c.1427C>A (p.Ala476Asp) rs202216463
NM_001199107.2(TBC1D24):c.1440G>A (p.Ser480=) rs12373107
NM_001199107.2(TBC1D24):c.1449G>C (p.Leu483=) rs753258278
NM_001199107.2(TBC1D24):c.1467C>T (p.Asn489=) rs779963634
NM_001199107.2(TBC1D24):c.1482C>G (p.Thr494=) rs373862230
NM_001199107.2(TBC1D24):c.1500G>A (p.Ala500=) rs201059992
NM_001199107.2(TBC1D24):c.1503G>A (p.Gly501=) rs368735897
NM_001199107.2(TBC1D24):c.1509C>T (p.Ser503=) rs189089167
NM_001199107.2(TBC1D24):c.1525+17G>A rs537260143
NM_001199107.2(TBC1D24):c.1525+6C>T rs758013935
NM_001199107.2(TBC1D24):c.1526-13G>A rs766052989
NM_001199107.2(TBC1D24):c.1545G>A (p.Ala515=) rs747350771
NM_001199107.2(TBC1D24):c.1570C>T (p.Arg524Trp) rs78644690
NM_001199107.2(TBC1D24):c.1620C>T (p.Ser540=) rs781723084
NM_001199107.2(TBC1D24):c.1641C>A (p.Ala547=) rs553215090
NM_001199107.2(TBC1D24):c.1642G>A (p.Val548Met) rs201649140
NM_001199107.2(TBC1D24):c.179G>A (p.Arg60Gln) rs200226466
NM_001199107.2(TBC1D24):c.207T>C (p.Pro69=) rs13339237
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.27C>T (p.Phe9=) rs759193465
NM_001199107.2(TBC1D24):c.297G>A (p.Thr99=) rs767766165
NM_001199107.2(TBC1D24):c.312C>T (p.Tyr104=) rs754301066
NM_001199107.2(TBC1D24):c.327C>A (p.Arg109=) rs754551693
NM_001199107.2(TBC1D24):c.327C>T (p.Arg109=) rs754551693
NM_001199107.2(TBC1D24):c.330C>T (p.Gly110=) rs779117497
NM_001199107.2(TBC1D24):c.441C>T (p.Asp147=) rs149371169
NM_001199107.2(TBC1D24):c.447C>T (p.Ala149=) rs755794991
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.492C>T (p.Pro164=) rs369172908
NM_001199107.2(TBC1D24):c.493G>A (p.Gly165Ser) rs200926225
NM_001199107.2(TBC1D24):c.546G>A (p.Thr182=) rs182825122
NM_001199107.2(TBC1D24):c.561G>T (p.Val187=) rs1555501246
NM_001199107.2(TBC1D24):c.570C>T (p.Tyr190=) rs917806963
NM_001199107.2(TBC1D24):c.579G>T (p.Ala193=) rs1394269760
NM_001199107.2(TBC1D24):c.641G>A (p.Arg214His) rs200324356
NM_001199107.2(TBC1D24):c.648G>C (p.Leu216=) rs571126287
NM_001199107.2(TBC1D24):c.651T>C (p.Phe217=) rs750100459
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.785C>T (p.Ser262Leu) rs201060500
NM_001199107.2(TBC1D24):c.792C>T (p.Ser264=) rs769290045
NM_001199107.2(TBC1D24):c.843C>G (p.Ser281=) rs1555501311
NM_001199107.2(TBC1D24):c.867G>A (p.Ala289=) rs1328290571
NM_001199107.2(TBC1D24):c.885C>G (p.Phe295Leu) rs72768728
NM_001199107.2(TBC1D24):c.903G>A (p.Gln301=) rs776739391
NM_001199107.2(TBC1D24):c.90T>C (p.Thr30=) rs575173753
NM_001199107.2(TBC1D24):c.948C>T (p.Ile316=) rs1057522754
NM_001199107.2(TBC1D24):c.951C>T (p.Thr317=) rs766745103
NM_001199107.2(TBC1D24):c.965+8G>A rs372247100
NM_001199107.2(TBC1D24):c.983+15_983+16del rs1064794673
NM_001199107.2(TBC1D24):c.984-5C>G rs535021783

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