"Genome-Nilou Lab"[submitter] AND "ALG8"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 96088	NM_024079.4(ALG8):c.*20A>G	ALG8	Single nucleotide variant	ALG8 congenital disorder of glycosylation +3 more	GBenign
Select item 1188963	NM_024079.5(ALG8):c.898+139C>T	ALG8	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 96092	NM_024079.5(ALG8):c.665A>G (p.Asn222Ser)	ALG8 (N222S)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 261680	NM_024079.5(ALG8):c.478+35A>T	ALG8	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 1188964	NM_024079.5(ALG8):c.174+30del	ALG8	Deletion (intron variant)	not provided +1 more	GBenign
Select item 261685	NM_024079.5(ALG8):c.95+23G>T	ALG8, LOC130006492	Single nucleotide variant (intron variant)	not specified +2 more	GBenign

ClinVar