List of variants in gene CACNB4 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000726.5(CACNB4):c.599-15G>A	rs41270209	0.00314
NM_000726.5(CACNB4):c.311G>T (p.Cys104Phe)	rs1805031	0.00074
NM_000726.5(CACNB4):c.771G>A (p.Thr257=)	rs2293219	0.00008
NM_000726.5(CACNB4):c.1233C>A (p.Thr411=)
NM_000726.5(CACNB4):c.699+15T>G
NM_000726.5(CACNB4):c.700-469G>A

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