List of variants in gene TBC1D24 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_001199107.2(TBC1D24):c.-7C>T	rs199852092	0.00126
NM_001199107.2(TBC1D24):c.1570C>T (p.Arg524Trp)	rs78644690	0.00035
NM_001199107.2(TBC1D24):c.179G>A (p.Arg60Gln)	rs200226466	0.00031
NM_001199107.2(TBC1D24):c.1038C>T (p.Ser346=)	rs377697825	0.00026
NM_001199107.2(TBC1D24):c.1503G>A (p.Gly501=)	rs368735897	0.00018
NM_001199107.2(TBC1D24):c.1302+14A>C	rs528462687	0.00009
NM_001199107.2(TBC1D24):c.1642G>A (p.Val548Met)	rs201649140	0.00009
NM_001199107.2(TBC1D24):c.1425C>T (p.Pro475=)	rs370869383	0.00008
NM_001199107.2(TBC1D24):c.243C>T (p.Ile81=)	rs745405784	0.00006
NM_001199107.2(TBC1D24):c.1125C>T (p.His375=)	rs749163517	0.00005
NM_001199107.2(TBC1D24):c.1142+14G>A	rs745904419	0.00004
NM_001199107.2(TBC1D24):c.330C>T (p.Gly110=)	rs779117497	0.00004
NM_001199107.2(TBC1D24):c.90T>C (p.Thr30=)	rs575173753	0.00003
NM_001199107.2(TBC1D24):c.951C>T (p.Thr317=)	rs766745103	0.00003
NM_001199107.2(TBC1D24):c.1467C>T (p.Asn489=)	rs779963634	0.00002
NM_001199107.2(TBC1D24):c.213C>T (p.Ala71=)	rs778212970	0.00002
NM_001199107.2(TBC1D24):c.297G>A (p.Thr99=)	rs767766165	0.00002
NM_001199107.2(TBC1D24):c.1545G>A (p.Ala515=)	rs747350771	0.00001
NM_001199107.2(TBC1D24):c.27C>T (p.Phe9=)	rs759193465	0.00001
NM_001199107.2(TBC1D24):c.1410C>A (p.Ser470=)	rs553497128
NM_001199107.2(TBC1D24):c.327C>T (p.Arg109=)	rs754551693
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

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