"Baylor Genetics"[submitter] AND "SLC35C1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 304736	NM_018389.5(SLC35C1):c.29G>A (p.Arg10Lys)	SLC35C1 (R10K)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases +2 more	GConflicting classifications of pathogenicity
Select item 1028108	NM_018389.5(SLC35C1):c.184C>G (p.Leu62Val)	SLC35C1 (L49V +1 more)	Single nucleotide variant (missense variant)	Leukocyte adhesion deficiency type II	GUncertain significance
Select item 965658	NM_018389.5(SLC35C1):c.375C>G (p.Ile125Met)	SLC35C1 (I112M +1 more)	Single nucleotide variant (missense variant)	Leukocyte adhesion deficiency type II	GUncertain significance
Select item 304742	NM_018389.5(SLC35C1):c.748G>A (p.Gly250Arg)	SLC35C1 (G250R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1028109	NM_018389.5(SLC35C1):c.969G>C (p.Trp323Cys)	SLC35C1 (W310C +1 more)	Single nucleotide variant (missense variant)	Leukocyte adhesion deficiency type II	GUncertain significance
Select item 1032799	NM_018389.5(SLC35C1):c.997G>A (p.Gly333Ser)	SLC35C1 (G333S +1 more)	Single nucleotide variant (missense variant)	Leukocyte adhesion deficiency type II	GUncertain significance

ClinVar