ClinVar Miner

List of variants in gene TBC1D24 reported as likely benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 26
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HGVS dbSNP
NM_001199107.2(TBC1D24):c.-7C>T rs199852092
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.1302+14A>C rs528462687
NM_001199107.2(TBC1D24):c.1425C>T (p.Pro475=) rs370869383
NM_001199107.2(TBC1D24):c.1467C>T (p.Asn489=) rs779963634
NM_001199107.2(TBC1D24):c.1503G>A (p.Gly501=) rs368735897
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.1642G>A (p.Val548Met) rs201649140
NM_001199107.2(TBC1D24):c.179G>A (p.Arg60Gln) rs200226466
NM_001199107.2(TBC1D24):c.213C>T (p.Ala71=) rs778212970
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.327C>T (p.Arg109=) rs754551693
NM_001199107.2(TBC1D24):c.330C>T (p.Gly110=) rs779117497
NM_001199107.2(TBC1D24):c.641G>A (p.Arg214His) rs200324356
NM_001199107.2(TBC1D24):c.702G>A (p.Val234=) rs188739853
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.903G>A (p.Gln301=) rs776739391
NM_001199107.2(TBC1D24):c.90T>C (p.Thr30=) rs575173753
NM_001199107.2(TBC1D24):c.951C>T (p.Thr317=) rs766745103

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