"PreventionGenetics, part of Exact Sciences"[submitter] AND "SLIT2"[ge - ClinVar

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Items: 45

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 712547	NM_004787.4(SLIT2):c.27G>C (p.Leu9=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder +1 more	GBenign
Select item 3031972	NM_004787.4(SLIT2):c.57C>A (p.Ile19=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder	GLikely benign
Select item 2634892	NM_004787.4(SLIT2):c.104C>T (p.Ser35Leu)	SLIT2 (S35L)	Single nucleotide variant (missense variant)	SLIT2-related disorder	GUncertain significance
Select item 2631823	NM_004787.4(SLIT2):c.260T>G (p.Met87Arg)	SLIT2 (M87R)	Single nucleotide variant (missense variant)	SLIT2-related disorder	GUncertain significance
Select item 745030	NM_004787.4(SLIT2):c.275G>A (p.Ser92Asn)	SLIT2 (S92N)	Single nucleotide variant (missense variant)	SLIT2-related disorder +1 more	GLikely benign
Select item 2634630	NM_004787.4(SLIT2):c.486G>C (p.Gln162His)	SLIT2 (Q162H)	Single nucleotide variant (missense variant)	SLIT2-related disorder	GUncertain significance
Select item 3050734	NM_004787.4(SLIT2):c.612-10T>C	SLIT2	Single nucleotide variant (intron variant)	SLIT2-related disorder	GLikely benign
Select item 3059102	NM_004787.4(SLIT2):c.776-967G>T	SLIT2	Single nucleotide variant (intron variant)	SLIT2-related disorder	GBenign
Select item 2752949	NM_004787.4(SLIT2):c.919T>C (p.Leu307=)	SLIT2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1469174	NM_004787.4(SLIT2):c.934A>G (p.Ile312Val)	SLIT2 (I312V +1 more)	Single nucleotide variant (missense variant)	SLIT2-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 775950	NM_004787.4(SLIT2):c.1044C>T (p.Arg348=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder +1 more	GBenign
Select item 3061601	NM_004787.4(SLIT2):c.1065C>T (p.Leu355=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder	GLikely benign
Select item 731090	NM_004787.4(SLIT2):c.1209A>G (p.Leu403=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder +1 more	GBenign/Likely benign
Select item 2906386	NM_004787.4(SLIT2):c.1233C>T (p.Ile411=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder +1 more	GLikely benign
Select item 2634793	NM_004787.4(SLIT2):c.1505C>T (p.Ala502Val)	SLIT2 (A494V +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 779875	NM_004787.4(SLIT2):c.1584G>A (p.Pro528=)	SLIT2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 717490	NM_004787.4(SLIT2):c.1620C>G (p.Leu540=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder +1 more	GBenign
Select item 1600438	NM_004787.4(SLIT2):c.1671T>C (p.Leu557=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder +1 more	GBenign
Select item 2040594	NM_004787.4(SLIT2):c.1678T>C (p.Leu560=)	SLIT2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2706141	NM_004787.4(SLIT2):c.1875T>C (p.Ser625=)	SLIT2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1601160	NM_004787.4(SLIT2):c.1956T>C (p.Thr652=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder +1 more	GBenign/Likely benign
Select item 2053014	NM_004787.4(SLIT2):c.2142C>T (p.Asp714=)	SLIT2	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 724945	NM_004787.4(SLIT2):c.2144-8C>T	SLIT2	Single nucleotide variant (intron variant)	SLIT2-related disorder +1 more	GLikely benign
Select item 3053940	NM_004787.4(SLIT2):c.2172T>G (p.Leu724=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder	GLikely benign
Select item 2632225	NM_004787.4(SLIT2):c.2519T>C (p.Val840Ala)	SLIT2 (V832A +2 more)	Single nucleotide variant (missense variant)	SLIT2-related disorder	GUncertain significance
Select item 3055501	NM_004787.4(SLIT2):c.2547T>C (p.Ser849=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder	GLikely benign
Select item 3035918	NM_004787.4(SLIT2):c.2700T>C (p.Thr900=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder	GLikely benign
Select item 1950435	NM_004787.4(SLIT2):c.2703C>T (p.Pro901=)	SLIT2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3029737	NM_004787.4(SLIT2):c.2767C>T (p.Leu923=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder	GLikely benign
Select item 3030912	NM_004787.4(SLIT2):c.2850+3A>C	SLIT2	Single nucleotide variant (intron variant)	SLIT2-related disorder	GLikely benign
Select item 3052013	NM_004787.4(SLIT2):c.3171A>G (p.Pro1057=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder	GLikely benign
Select item 2159902	NM_004787.4(SLIT2):c.3204C>T (p.Tyr1068=)	SLIT2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3051488	NM_004787.4(SLIT2):c.3219C>T (p.Cys1073=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder	GLikely benign
Select item 725747	NM_004787.4(SLIT2):c.3220G>C (p.Asp1074His)	SLIT2 (D1066H +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3031150	NM_004787.4(SLIT2):c.3234C>T (p.Asp1078=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder	GLikely benign
Select item 719034	NM_004787.4(SLIT2):c.3288C>T (p.Asn1096=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder +1 more	GBenign
Select item 2143589	NM_004787.4(SLIT2):c.3309C>T (p.Pro1103=)	SLIT2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2076174	NM_004787.4(SLIT2):c.3336G>A (p.Glu1112=)	SLIT2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3052989	NM_004787.4(SLIT2):c.3592C>T (p.Leu1198=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder	GLikely benign
Select item 3030929	NM_004787.4(SLIT2):c.3669T>C (p.Ser1223=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder	GLikely benign
Select item 770351	NM_004787.4(SLIT2):c.4049G>A (p.Ser1350Asn)	SLIT2 (S1350N +2 more)	Single nucleotide variant (missense variant)	SLIT2-related disorder +1 more	GBenign/Likely benign
Select item 1584925	NM_004787.4(SLIT2):c.4137-4G>A	SLIT2	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 775213	NM_004787.4(SLIT2):c.4253C>T (p.Ala1418Val)	SLIT2 (A1418V +2 more)	Single nucleotide variant (missense variant)	SLIT2-related disorder +1 more	GBenign/Likely benign
Select item 2043554	NM_004787.4(SLIT2):c.4542C>T (p.Asp1514=)	SLIT2	Single nucleotide variant (synonymous variant)	SLIT2-related disorder +1 more	GLikely benign
Select item 3034384	NM_004787.4(SLIT2):c.*10C>T	SLIT2	Single nucleotide variant (3 prime UTR variant)	SLIT2-related disorder	GLikely benign

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Items: 45