"SLIT3-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2635824	NM_003062.4(SLIT3):c.10_17del	SLIT3	Deletion (3 prime UTR variant)	SLIT3-related disorder	GUncertain significance
Select item 2656043	NM_003062.4(SLIT3):c.4506G>A (p.Thr1502=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2635033	NM_003062.4(SLIT3):c.4455G>T (p.Gln1485His)	SLIT3 (Q1485H +1 more)	Single nucleotide variant (missense variant)	SLIT3-related disorder	GUncertain significance
Select item 2656046	NM_003062.4(SLIT3):c.4053G>A (p.Val1351=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2206469	NM_003062.4(SLIT3):c.4044G>T (p.Lys1348Asn)	SLIT3 (K1348N +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3040777	NM_003062.4(SLIT3):c.3903C>T (p.Gly1301=)	SLIT3	Single nucleotide variant (synonymous variant)	SLIT3-related disorder	GBenign
Select item 711944	NM_003062.4(SLIT3):c.3505G>C (p.Val1169Leu)	SLIT3 (V1169L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3047769	NM_003062.4(SLIT3):c.3088C>T (p.Leu1030=)	SLIT3	Single nucleotide variant (synonymous variant)	SLIT3-related disorder	GLikely benign
Select item 3029294	NM_003062.4(SLIT3):c.2991A>G (p.Pro997=)	SLIT3	Single nucleotide variant (synonymous variant)	SLIT3-related disorder	GLikely benign
Select item 3034009	NM_003062.4(SLIT3):c.2333C>A (p.Thr778Lys)	SLIT3 (T778K)	Single nucleotide variant (missense variant)	SLIT3-related disorder	GUncertain significance
Select item 726060	NM_003062.4(SLIT3):c.2169G>A (p.Pro723=)	SLIT3	Single nucleotide variant (synonymous variant)	SLIT3-related disorder +1 more	GLikely benign
Select item 3047539	NM_003062.4(SLIT3):c.1804C>T (p.Arg602Cys)	SLIT3 (R602C)	Single nucleotide variant (missense variant)	SLIT3-related disorder	GLikely benign
Select item 3024729	NM_003062.4(SLIT3):c.1481G>C (p.Arg494Thr)	SLIT3 (R494T)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2656062	NM_003062.4(SLIT3):c.1323C>T (p.Cys441=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3046000	NM_003062.4(SLIT3):c.937C>T (p.Arg313Cys)	SLIT3 (R313C)	Single nucleotide variant (missense variant)	SLIT3-related disorder	GLikely benign
Select item 3056199	NM_003062.4(SLIT3):c.699A>G (p.Arg233=)	SLIT3	Single nucleotide variant (synonymous variant)	SLIT3-related disorder	GLikely benign