List of variants in gene TBC1D24 reported as not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001199107.2(TBC1D24):c.169C>T (p.Arg57Cys)	rs202162520	0.00121
NM_001199107.2(TBC1D24):c.1008del (p.His336fs)	rs398122967	0.00005
NM_001199107.2(TBC1D24):c.724C>T (p.Arg242Cys)	rs398122965	0.00003
NM_001199107.2(TBC1D24):c.119G>T (p.Arg40Leu)	rs760474458	0.00001
NM_001199107.2(TBC1D24):c.533C>T (p.Ser178Leu)	rs483352866	0.00001
NM_001199107.2(TBC1D24):c.679C>T (p.Arg227Trp)	rs748302886	0.00001
NM_001199107.2(TBC1D24):c.1142+272T>C	rs2141874790
NM_001199107.2(TBC1D24):c.208G>T (p.Asp70Tyr)	rs587777147
NM_001199107.2(TBC1D24):c.404C>T (p.Pro135Leu)	rs1057519630
NM_001199107.2(TBC1D24):c.752del (p.Phe251fs)	rs766769998

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