ClinVar Miner

List of variants in gene CACNA1G reported as likely pathogenic 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_018896.5(CACNA1G):c.1103C>T (p.Ser368Phe)	rs1160501227
NM_018896.5(CACNA1G):c.4601G>A (p.Gly1534Asp)	rs1598588782

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