Related gene-specific medical variations for Gene (Select 55343) - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2428634	NM_018389.5(SLC35C1):c.847G>A (p.Val283Met)	SLC35C1 (V270M +1 more)	Single nucleotide variant (missense variant)	Leukocyte adhesion deficiency type II	GUncertain significance
Select item 1283904	NM_001145265.1(SLC35C1):c.-154G>A	LOC130005624, SLC35C1	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 877526	NM_018389.5(SLC35C1):c.-615G>C	LOC130005625, SLC35C1	Single nucleotide variant (5 prime UTR variant +1 more)	Leukocyte adhesion deficiency type II	GUncertain significance
Select item 304728	NM_018389.5(SLC35C1):c.-481G>A	LOC130005625, SLC35C1	Single nucleotide variant (5 prime UTR variant +1 more)	Leukocyte adhesion deficiency type II	GUncertain significance
Select item 304727	NM_018389.5(SLC35C1):c.-518C>A	LOC130005625, SLC35C1	Single nucleotide variant (5 prime UTR variant +1 more)	Leukocyte adhesion deficiency type II	GUncertain significance
Select item 304726	NM_018389.5(SLC35C1):c.-546_-540dup	LOC130005625, SLC35C1	Duplication (5 prime UTR variant +1 more)	Congenital disorder of glycosylation	GUncertain significance
Select item 304725	NM_018389.5(SLC35C1):c.-569C>T	LOC130005625, SLC35C1	Single nucleotide variant (5 prime UTR variant +1 more)	Leukocyte adhesion deficiency type II	GUncertain significance
Select item 161533	NM_018389.5(SLC35C1):c.556G>A (p.Asp186Asn)	SLC35C1 (D173N +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance