Related gene-specific medical variations for Gene (Select 6586) - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2656055	NM_003062.4(SLIT3):c.2559G>A (p.Ala853=)	SLIT3, SLIT3-AS2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656054	NM_003062.4(SLIT3):c.2805T>C (p.Pro935=)	SLIT3, SLIT3-AS2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2582364	NM_003062.4(SLIT3):c.691C>T (p.Arg231Ter)	SLIT3 (R231*)	Single nucleotide variant (nonsense)	SLIT3-related anomalies of the kidney and urinary tract	GUncertain significance
Select item 2582303	NM_003062.4(SLIT3):c.1604C>A (p.Thr535Asn)	SLIT3 (T535N)	Single nucleotide variant (missense variant)	SLIT3-related anomalies of the kidney and urinary tract	GUncertain significance
Select item 2517535	NM_003062.4(SLIT3):c.1145A>G (p.Gln382Arg)	LOC126807586, SLIT3 (Q382R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2498992	NM_003062.4(SLIT3):c.2643C>T (p.Ile881=)	SLIT3, SLIT3-AS2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2469848	NM_003062.4(SLIT3):c.1105G>A (p.Glu369Lys)	LOC126807586, SLIT3 (E369K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2441892	NM_003062.4(SLIT3):c.2045G>A (p.Arg682Gln)	SLIT3 (R682Q)	Single nucleotide variant (missense variant)	SLIT3-related anomalies of the kidney and urinary tract	GUncertain significance
Select item 2441867	NM_003062.4(SLIT3):c.2393T>C (p.Met798Thr)	SLIT3 (M798T)	Single nucleotide variant (missense variant)	SLIT3-related anomalies of the kidney and urinary tract	GUncertain significance
Select item 2441796	NM_003062.4(SLIT3):c.2483+1967A>G	SLIT3, SLIT3-AS2	Single nucleotide variant (non-coding transcript variant +1 more)	SLIT3-related anomalies of the kidney and urinary tract	GUncertain significance
Select item 2380260	NM_003062.4(SLIT3):c.2621C>T (p.Ala874Val)	SLIT3-AS2, SLIT3 (A874V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2378207	NM_003062.4(SLIT3):c.583C>T (p.Arg195Cys)	LOC126807587, SLIT3 (R195C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2241457	NM_003062.4(SLIT3):c.2531A>G (p.Asn844Ser)	LOC126807585, SLIT3 +1 more (N844S)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1302224	NM_003062.4(SLIT3):c.558-14G>C	LOC126807587, SLIT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 780981	NM_003062.4(SLIT3):c.2555+9C>T	LOC126807585, SLIT3 +1 more	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 769672	NM_003062.4(SLIT3):c.1112= (p.Val371=)	LOC126807586, SLIT3	Variation (no sequence alteration)	not provided	GBenign
Select item 769671	NM_003062.4(SLIT3):c.2533G>A (p.Asp845Asn)	LOC126807585, SLIT3 +1 more (D845N)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 723995	NM_003062.4(SLIT3):c.2719+9C>T	SLIT3-AS2, SLIT3	Single nucleotide variant (intron variant)	not provided	GBenign