"Clinical Genetics, Academic Medical Center"[submitter] AND "SELENON"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 130284	NM_020451.3(SELENON):c.409A>G (p.Thr137Ala)	SELENON (T137A +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 95963	NM_020451.3(SELENON):c.425G>A (p.Cys142Tyr)	SELENON (C142Y +1 more)	Single nucleotide variant (missense variant)	SEPN1-related disorder +3 more	GBenign
Select item 95967	NM_020451.3(SELENON):c.981C>T (p.Arg327=)	SELENON	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 212146	NM_020451.3(SELENON):c.1092+6C>G	SELENON	Single nucleotide variant (intron variant)	not specified +3 more	GBenign/Likely benign
Select item 95956	NM_020451.3(SELENON):c.1173T>C (p.Pro391=)	SELENON	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 95959	NM_020451.3(SELENON):c.1506C>A (p.Asn502Lys)	SELENON (N502K +1 more)	Single nucleotide variant (missense variant)	SEPN1-related disorder +3 more	GBenign

ClinVar