List of variants in gene ALG12 reported as likely benign for ALG12-congenital disorder of glycosylation

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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
NM_024105.4(ALG12):c.1068C>T (p.Ala356=)	rs371321442
NM_024105.4(ALG12):c.1299C>T (p.Leu433=)	rs150614794
NM_024105.4(ALG12):c.207C>T (p.Leu69=)	rs765297992
NM_024105.4(ALG12):c.240C>T (p.Pro80=)	rs773878720
NM_024105.4(ALG12):c.469+13C>T	rs78916708
NM_024105.4(ALG12):c.48G>C (p.Leu16=)	rs143508665
NM_024105.4(ALG12):c.55G>A (p.Ala19Thr)	rs138266806
NM_024105.4(ALG12):c.57C>T (p.Ala19=)	rs763942380
NM_024105.4(ALG12):c.631C>T (p.Arg211Cys)	rs144665682
NM_024105.4(ALG12):c.645G>A (p.Pro215=)	rs12167668
NM_024105.4(ALG12):c.698G>A (p.Arg233Gln)	rs114264124
NM_024105.4(ALG12):c.867C>T (p.His289=)	rs147801200
NM_024105.4(ALG12):c.939C>T (p.Ile313=)	rs114335781

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