List of variants in gene CACNA1C reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_000719.7(CACNA1C):c.617+17G>A	rs1544515	0.27035
NM_000719.7(CACNA1C):c.3786C>T (p.Phe1262=)	rs216008	0.20673
NM_000719.7(CACNA1C):c.5292C>T (p.Asn1764=)	rs72552065	0.04512
NM_000719.7(CACNA1C):c.5680+15C>T	rs114036394	0.01782
NM_000719.7(CACNA1C):c.5649G>A (p.Pro1883=)	rs56270948	0.01676
NM_000719.7(CACNA1C):c.5383G>A (p.Gly1795Arg)	rs111298509	0.01614
NM_000719.7(CACNA1C):c.171C>T (p.Asp57=)	rs34419050	0.01584
NM_000719.7(CACNA1C):c.213G>A (p.Ala71=)	rs113869350	0.01399
NM_000719.7(CACNA1C):c.5604A>G (p.Gln1868=)	rs11062316	0.00963
NM_000719.7(CACNA1C):c.771C>T (p.Val257=)	rs112315742	0.00908
NM_000719.7(CACNA1C):c.371+17G>A	rs78645318	0.00797
NM_000719.7(CACNA1C):c.5097C>T (p.Ala1699=)	rs113595214	0.00709
NM_000719.7(CACNA1C):c.3114G>C (p.Leu1038=)	rs114139824	0.00585
NM_000719.7(CACNA1C):c.3387G>A (p.Thr1129=)	rs188224114	0.00525
NM_000719.7(CACNA1C):c.5064C>T (p.Ser1688=)	rs139872789	0.00449
NM_000719.7(CACNA1C):c.5091+18G>A	rs143343491	0.00423
NM_000719.7(CACNA1C):c.2449C>T (p.Pro817Ser)	rs112532048	0.00279
NM_000719.7(CACNA1C):c.1176G>T (p.Gly392=)	rs1051360	0.00209
NM_000719.7(CACNA1C):c.1794C>T (p.Gly598=)	rs116491041	0.00200
NM_000719.7(CACNA1C):c.5665C>T (p.Arg1889Cys)	rs185788586	0.00182
NM_000719.7(CACNA1C):c.1669+10G>A	rs576194052	0.00175
NM_000719.7(CACNA1C):c.4624-9C>T	rs377568567	0.00163
NM_000719.7(CACNA1C):c.3780C>A (p.Gly1260=)	rs201258230	0.00131
NM_000719.7(CACNA1C):c.1074G>A (p.Gln358=)	rs139842134	0.00113
NM_000719.7(CACNA1C):c.4956+17G>A	rs200706151	0.00103
NM_000719.7(CACNA1C):c.3049-10C>T	rs186741807	0.00093
NM_000719.7(CACNA1C):c.846C>T (p.Tyr282=)	rs200847105	0.00027
NM_000719.7(CACNA1C):c.5478G>A (p.Ala1826=)	rs200283756	0.00023
NM_000719.7(CACNA1C):c.5593G>A (p.Glu1865Lys)	rs200231105	0.00012
NM_000719.7(CACNA1C):c.5445-586_5445-584delinsTGG	rs71441836
NM_000719.7(CACNA1C):c.5680+11C>T	rs66611965

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