SLC35F2[gene] - ClinVar

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Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 148976	GRCh38/hg38 11q14.3-22.3(chr11:91086659-109595582)x1	LOC130006596, LOC130006597 +387 more	Copy number loss	See cases	GPathogenic
Select item 59772	GRCh38/hg38 11q22.1-25(chr11:100348599-135040246)x3	AASDHPPT, ABCG4 +1199 more	Copy number gain	See cases	GPathogenic
Select item 147281	GRCh38/hg38 11q22.3(chr11:107479091-108222532)x1	ACAT1, ALKBH8 +28 more	Copy number loss	See cases	GPathogenic
Select item 151258	GRCh38/hg38 11q22.3(chr11:107656034-107998014)x3	ELMOD1, LOC126861330 +10 more	Copy number gain	See cases	GLikely benign
Select item 157225	CM000673.1:g.107653081_107683596dup	SLC35F2	Duplication	Gestational diabetes mellitus uncontrolled	Gnot provided
Select item 157226	NC_000011.10:g.107788298_107799502dup	SLC35F2	Duplication	Gestational diabetes mellitus uncontrolled	Gnot provided
Select item 3164414	NM_017515.5(SLC35F2):c.1063A>G (p.Ile355Val)	SLC35F2 (I355V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319619	NM_017515.5(SLC35F2):c.1057A>G (p.Ile353Val)	SLC35F2 (I353V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164413	NM_017515.5(SLC35F2):c.1016C>T (p.Thr339Met)	SLC35F2 (T339M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164412	NM_017515.5(SLC35F2):c.1012C>T (p.Arg338Cys)	SLC35F2 (R338C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360043	NM_017515.5(SLC35F2):c.953A>G (p.Tyr318Cys)	SLC35F2 (Y318C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601086	NM_017515.5(SLC35F2):c.871G>A (p.Val291Ile)	SLC35F2 (V291I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265510	NM_017515.5(SLC35F2):c.848T>C (p.Ile283Thr)	SLC35F2 (I283T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207029	NM_017515.5(SLC35F2):c.796G>A (p.Val266Met)	SLC35F2 (V266M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305369	NM_017515.5(SLC35F2):c.780A>T (p.Lys260Asn)	SLC35F2 (K260N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318858	NM_017515.5(SLC35F2):c.715A>G (p.Ile239Val)	SLC35F2 (I239V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483182	NM_017515.5(SLC35F2):c.650A>T (p.Glu217Val)	SLC35F2 (E217V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210409	NM_017515.5(SLC35F2):c.502G>A (p.Val168Met)	SLC35F2 (V168M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510035	NM_017515.5(SLC35F2):c.275C>T (p.Ala92Val)	SLC35F2 (A92V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164415	NM_017515.5(SLC35F2):c.16C>T (p.Pro6Ser)	LOC130006688, SLC35F2 (P6S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2671625	Single allele	AASDHPPT, ABCG4 +275 more	Duplication	not provided	GPathogenic
Select item 1807688	GRCh37/hg19 11q22.1-22.3(chr11:101371503-109306519)x1	ACAT1, ALKBH8 +47 more	Copy number loss	not provided	GPathogenic
Select item 1704646	GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3	MAML2, MAP3K11 +955 more	Copy number gain	MISSED ABORTION	GPathogenic
Select item 1340355	GRCh37/hg19 11q22.3(chr11:107582884-107838385)x3	RAB39A, SLC35F2	Copy number gain	not provided	GLikely benign
Select item 1340004	GRCh37/hg19 11q14.1-23.3(chr11:85422071-118022671)x1	AASDHPPT, ACAT1 +182 more	Copy number loss	not provided	GUncertain significance
Select item 1075501	NC_000011.9:g.(?_94153285)_(111965700_?)del	FDXACB1, FUT4 +94 more	Deletion	Ataxia-telangiectasia syndrome	GPathogenic
Select item 997825	Single allele	MMP13, MMP20 +904 more	Deletion	Intellectual disability	GPathogenic
Select item 973579	NC_000011.9:g.104288964_134937416dup	VSIG2, VWA5A +259 more	Duplication	Distal trisomy 11q	GPathogenic
Select item 815468	GRCh37/hg19 11q22.3-23.3(chr11:105699599-114524876)x1	AASDHPPT, ACAT1 +68 more	Copy number loss	not provided	GPathogenic
Select item 815462	GRCh37/hg19 11q22.3-23.2(chr11:103320065-114349787)x1	AASDHPPT, ACAT1 +76 more	Copy number loss	not provided	GPathogenic
Select item 688419	GRCh37/hg19 11q22.3(chr11:107546688-108077391)x3	ACAT1, CUL5 +4 more	Copy number gain	not provided	GUncertain significance
Select item 688050	GRCh37/hg19 11q22.3-23.3(chr11:104101411-116680918)x1	AASDHPPT, ACAT1 +80 more	Copy number loss	not provided	GPathogenic
Select item 563885	GRCh37/hg19 11q13.4-23.3(chr11:71588805-116680918)x3	AAMDC, AASDHPPT +261 more	Copy number gain	not provided	GPathogenic
Select item 441904	GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)	AAMDC, AASDHPPT +1289 more	Copy number gain	See cases	GPathogenic
Select item 441903	GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3	SLC37A4, SNORD26 +1289 more	Copy number gain	See cases	GPathogenic
Select item 441837	GRCh37/hg19 11q14.2-22.3(chr11:88152458-109414650)x1	AASDHPPT, ACAT1 +95 more	Copy number loss	See cases	GPathogenic
Select item 394232	GRCh37/hg19 11q22.3(chr11:107537206-107925627)x3	CUL5, ELMOD1 +3 more	Copy number gain	See cases	GLikely benign
Select item 221844	GRCh37/hg19 11q22.3(chr11:107554267-108004957)x3	SLN, ACAT1 +3 more	Copy number gain	Premature ovarian failure	GBenign

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Items: 38