List of variants in gene TBC1D24 reported as likely benign by Illumina Laboratory Services, Illumina

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.*4278C>G	rs74462094	0.00822
NM_001199107.2(TBC1D24):c.885C>G (p.Phe295Leu)	rs72768728	0.00609
NM_001199107.2(TBC1D24):c.*3235T>G	rs187125185	0.00402
NM_001199107.2(TBC1D24):c.*3370C>T	rs79502522	0.00360
NM_001199107.2(TBC1D24):c.1500G>A (p.Ala500=)	rs201059992	0.00334
NM_001199107.2(TBC1D24):c.1326C>T (p.Tyr442=)	rs184639841	0.00324
NM_001199107.2(TBC1D24):c.*3218T>G	rs564761307	0.00216
NM_001199107.2(TBC1D24):c.441C>T (p.Asp147=)	rs149371169	0.00200
NM_001199107.2(TBC1D24):c.1002C>T (p.Ala334=)	rs184389316	0.00160
NM_001199107.2(TBC1D24):c.*3750C>T	rs189487145	0.00155
NM_001199107.2(TBC1D24):c.169C>T (p.Arg57Cys)	rs202162520	0.00121
NM_001199107.2(TBC1D24):c.*622C>T	rs181012332	0.00100
NM_001199107.2(TBC1D24):c.*1233C>T	rs74621956	0.00066
NM_001199107.2(TBC1D24):c.204G>A (p.Thr68=)	rs201374999	0.00038
NM_001199107.2(TBC1D24):c.22T>C (p.Cys8Arg)	rs77585883	0.00024
NM_001199107.2(TBC1D24):c.1074C>T (p.Pro358=)	rs75961715	0.00021
NM_001199107.2(TBC1D24):c.*2001A>G	rs529770652	0.00020
NM_001199107.2(TBC1D24):c.*4677G>A	rs145113614	0.00019
NM_001199107.2(TBC1D24):c.663C>T (p.Pro221=)	rs148670169	0.00019
NM_001199107.2(TBC1D24):c.*1259G>A	rs545082961	0.00012
NM_001199107.2(TBC1D24):c.1642G>A (p.Val548Met)	rs201649140	0.00009
NM_001199107.2(TBC1D24):c.965+11G>A	rs568663296	0.00002
NM_001199107.2(TBC1D24):c.*2540del	rs58172016
NM_001199107.2(TBC1D24):c.2850_2851del	rs376511845
NM_001199107.2(TBC1D24):c.*36G>A	rs73490289
NM_001199107.2(TBC1D24):c.*3959G>A	rs550975150

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