List of variants in gene CACNA1A reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001127222.2(CACNA1A):c.6657T>C (p.His2219=)	rs16051	0.67380
NM_001127222.2(CACNA1A):c.3310G>A (p.Gly1104Ser)	rs16027	0.07737
NM_001127222.2(CACNA1A):c.6342C>G (p.Thr2114=)	rs16049	0.00467
NM_001127222.2(CACNA1A):c.1357G>A (p.Ala453Thr)	rs41276886	0.00451
NM_001127222.2(CACNA1A):c.5067+20G>A	rs184517632	0.00390
NM_001127222.2(CACNA1A):c.7262C>T (p.Pro2421Leu)	rs573961089	0.00130
NM_001127222.2(CACNA1A):c.1518T>C (p.Val506=)	rs16009	0.00114
NM_001127222.2(CACNA1A):c.1199-17G>C	rs190836274	0.00034
NM_001127222.2(CACNA1A):c.1983T>C (p.Phe661=)	rs368033271	0.00016
NM_001127222.2(CACNA1A):c.7328C>T (p.Ala2443Val)	rs763414737	0.00013
NM_001127222.2(CACNA1A):c.6061G>A (p.Glu2021Lys)	rs202002033	0.00010
NM_001127222.2(CACNA1A):c.6527-16C>T	rs752985059	0.00007
NM_001127222.2(CACNA1A):c.3601AAG[1] (p.Lys1202del)	rs772989979

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