List of variants in gene SELENON reported 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
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_020451.3(SELENON):c.1645G>A (p.Val549Met)	rs147131452	0.00268
NM_020451.3(SELENON):c.1715C>A (p.Thr572Asn)	rs183272965	0.00124
NM_020451.3(SELENON):c.415G>A (p.Ala139Thr)	rs201692549	0.00054
NM_020451.3(SELENON):c.943G>A (p.Gly315Ser)	rs121908188	0.00030
NM_020451.3(SELENON):c.4G>T (p.Gly2Cys)	rs982364753	0.00028
NM_020451.3(SELENON):c.1A>G (p.Met1Val)	rs121908184	0.00005
NM_020451.3(SELENON):c.988C>T (p.Arg330Trp)	rs1489695877	0.00002
NM_020451.3(SELENON):c.872G>A (p.Arg291Gln)	rs199564797	0.00001
NM_020451.3(SELENON):c.402_403+2del	rs773670891
NM_020451.3(SELENON):c.713dup (p.Asn238fs)	rs368104077

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