Related gene-specific medical variations for Gene (Select 6585) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3320486	NM_003061.3(SLIT1):c.224G>A (p.Arg75Gln)	ARHGAP19-SLIT1, SLIT1 (R75Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2640735	NM_003061.3(SLIT1):c.252C>A (p.Leu84=)	ARHGAP19-SLIT1, SLIT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2527970	NM_003061.3(SLIT1):c.131C>A (p.Thr44Lys)	ARHGAP19-SLIT1, SLIT1 (T44K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478937	NM_003061.3(SLIT1):c.76G>C (p.Ala26Pro)	ARHGAP19-SLIT1, SLIT1 (A26P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346226	NM_003061.3(SLIT1):c.43C>T (p.Arg15Trp)	ARHGAP19-SLIT1, SLIT1 (R15W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326757	NM_003061.3(SLIT1):c.26C>T (p.Ser9Phe)	ARHGAP19-SLIT1, SLIT1 (S9F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274367	NM_003061.3(SLIT1):c.334G>C (p.Glu112Gln)	ARHGAP19-SLIT1, SLIT1 (E112Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2268822	NM_003061.3(SLIT1):c.211A>T (p.Asn71Tyr)	ARHGAP19-SLIT1, SLIT1 (N71Y)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2243812	NM_003061.3(SLIT1):c.326A>G (p.Lys109Arg)	ARHGAP19-SLIT1, SLIT1 (K109R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance