ClinVar Miner

List of variants in gene TBC1D24 reported as likely benign by Ambry Genetics

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Total variants: 15
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HGVS dbSNP
NM_001199107.1(TBC1D24):c.1002C>T (p.Ala334=) rs184389316
NM_001199107.1(TBC1D24):c.1074C>T (p.Pro358=) rs75961715
NM_001199107.1(TBC1D24):c.1503G>A (p.Gly501=) rs368735897
NM_001199107.1(TBC1D24):c.1641C>A (p.Ala547=) rs553215090
NM_001199107.1(TBC1D24):c.204G>A (p.Thr68=) rs201374999
NM_001199107.1(TBC1D24):c.285C>T (p.Phe95=) rs774354974
NM_001199107.1(TBC1D24):c.396C>T (p.Pro132=)
NM_001199107.1(TBC1D24):c.441C>T (p.Asp147=) rs149371169
NM_001199107.1(TBC1D24):c.447C>T (p.Ala149=) rs755794991
NM_001199107.1(TBC1D24):c.493G>A (p.Gly165Ser) rs200926225
NM_001199107.1(TBC1D24):c.546G>A (p.Thr182=) rs182825122
NM_001199107.1(TBC1D24):c.813G>A (p.Thr271=)
NM_001199107.1(TBC1D24):c.951C>T (p.Thr317=) rs766745103
NM_020705.2(TBC1D24):c.1308C>T (p.Tyr436=) rs184639841
NM_020705.2(TBC1D24):c.1482G>A (p.Ala494=) rs201059992

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