List of variants in gene SCN4A 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000334.4(SCN4A):c.1796A>G (p.His599Arg)	rs187401185	0.00343
NM_000334.4(SCN4A):c.355G>A (p.Val119Ile)	rs41280110	0.00232
NM_000334.4(SCN4A):c.248T>C (p.Leu83Pro)	rs147352060	0.00141
NM_000334.4(SCN4A):c.1462G>A (p.Ala488Thr)	rs185941768	0.00059
NM_000334.4(SCN4A):c.952T>C (p.Trp318Arg)	rs199676994	0.00059
NM_000334.4(SCN4A):c.999C>T (p.Asn333=)	rs149726115	0.00056
NM_000334.4(SCN4A):c.1653C>T (p.Cys551=)	rs201199086	0.00026
NM_000334.4(SCN4A):c.1710C>T (p.Ile570=)	rs760067411	0.00005
NM_000334.4(SCN4A):c.364C>T (p.Arg122Cys)	rs150158100	0.00005
NM_000334.4(SCN4A):c.1575C>T (p.Ser525=)	rs376538198	0.00001
NM_000334.4(SCN4A):c.1038G>A (p.Gly346=)
NM_000334.4(SCN4A):c.1473G>A (p.Leu491=)
NM_000334.4(SCN4A):c.483-5C>A	rs191547933
NM_000334.4(SCN4A):c.704-6G>C	rs368225907

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