List of variants in gene VAC14 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_018052.5(VAC14):c.358A>G (p.Ile120Val)	rs145208697	0.00454
NM_018052.5(VAC14):c.880C>T (p.Leu294=)	rs146617185	0.00256
NM_018052.5(VAC14):c.612G>A (p.Ser204=)	rs144822178	0.00179
NM_018052.5(VAC14):c.1896G>A (p.Thr632=)	rs146202088	0.00076
NM_018052.5(VAC14):c.1761C>T (p.His587=)	rs200282045	0.00039
NM_018052.5(VAC14):c.492T>C (p.Ile164=)	rs113251587	0.00028
NM_018052.5(VAC14):c.873C>T (p.Arg291=)	rs200285981	0.00018
NM_018052.5(VAC14):c.2124C>T (p.Ser708=)	rs140883176	0.00016
NM_018052.5(VAC14):c.2244C>T (p.Tyr748=)	rs147699666	0.00009
NM_018052.5(VAC14):c.894C>T (p.Ser298=)	rs142446813	0.00005
NM_018052.5(VAC14):c.378C>T (p.Gly126=)	rs574284363	0.00002
NM_018052.5(VAC14):c.1320G>T (p.Thr440=)
NM_018052.5(VAC14):c.1356G>A (p.Ser452=)
NM_018052.5(VAC14):c.138C>A (p.Thr46=)
NM_018052.5(VAC14):c.2115G>A (p.Pro705=)	rs2278983
NM_018052.5(VAC14):c.2186+825G>A

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