List of variants in gene CACNA1I reported as benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_021096.4(CACNA1I):c.2157T>C (p.Ile719=)	rs5757761	0.65495
NM_021096.4(CACNA1I):c.1866C>T (p.Cys622=)	rs58955204	0.01712
NM_021096.4(CACNA1I):c.1503C>T (p.Leu501=)	rs57911777	0.00809
NM_021096.4(CACNA1I):c.2610C>T (p.Asp870=)	rs61708088	0.00619
NM_021096.4(CACNA1I):c.777G>A (p.Pro259=)	rs149938037	0.00609
NM_021096.4(CACNA1I):c.2529C>T (p.Val843=)	rs143888179	0.00551
NM_021096.4(CACNA1I):c.5268T>C (p.His1756=)	rs59305953	0.00514
NM_021096.4(CACNA1I):c.4269C>T (p.Leu1423=)	rs55968092	0.00433
NM_021096.4(CACNA1I):c.5056-5C>T	rs146526127	0.00407
NM_021096.4(CACNA1I):c.3810C>T (p.Val1270=)	rs184194154	0.00367
NM_021096.4(CACNA1I):c.819C>T (p.Gly273=)	rs111404878	0.00307
NM_021096.4(CACNA1I):c.1599G>A (p.Ala533=)	rs60658758	0.00279
NM_021096.4(CACNA1I):c.489C>T (p.Val163=)	rs60795524	0.00200
NM_021096.4(CACNA1I):c.4500C>T (p.Asn1500=)	rs142211910	0.00032
NM_021096.4(CACNA1I):c.1296C>T (p.Gly432=)
NM_021096.4(CACNA1I):c.1747G>A (p.Ala583Thr)
NM_021096.4(CACNA1I):c.3579G>C (p.Gln1193His)
NM_021096.4(CACNA1I):c.5285C>T (p.Pro1762Leu)
NM_021096.4(CACNA1I):c.5401C>A (p.Leu1801Met)

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