List of variants in gene SLC35A1 reported as uncertain significance for congenital disorder of glycosylation type II

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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: 16

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HGVS	dbSNP	gnomAD frequency
NM_006416.5(SLC35A1):c.890T>G (p.Leu297Arg)	rs201507608	0.00010
NM_006416.5(SLC35A1):c.1007G>A (p.Gly336Asp)	rs200065902	0.00004
NM_006416.5(SLC35A1):c.1000G>A (p.Val334Ile)	rs768492481	0.00001
NM_006416.5(SLC35A1):c.171G>T (p.Leu57Phe)	rs76193993	0.00001
NM_006416.5(SLC35A1):c.379T>A (p.Cys127Ser)	rs1242388466	0.00001
NM_006416.5(SLC35A1):c.569T>C (p.Phe190Ser)	rs763621828	0.00001
NM_006416.5(SLC35A1):c.475C>T (p.Gln159Ter)
NM_006416.5(SLC35A1):c.523TTA[1] (p.Leu176del)
NM_006416.5(SLC35A1):c.639G>A (p.Met213Ile)
NM_006416.5(SLC35A1):c.699T>G (p.Ile233Met)	rs150233994
NM_006416.5(SLC35A1):c.757G>C (p.Ala253Pro)	rs1484245900
NM_006416.5(SLC35A1):c.763G>C (p.Val255Leu)	rs550275644
NM_006416.5(SLC35A1):c.7G>A (p.Ala3Thr)
NM_006416.5(SLC35A1):c.855T>G (p.Ile285Met)
NM_006416.5(SLC35A1):c.883A>C (p.Ile295Leu)	rs2127977717
NM_006416.5(SLC35A1):c.908C>G (p.Thr303Ser)	rs2127978566

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