Cxcl3 Variant Search Result - Rat Genome Database

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12 records found for search term Cxcl3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155903887	CV2298701	single nucleotide variant	NM_002090.3(CXCL3):c.5C>G (p.Ala2Gly)	not specified [RCV004156276]	uncertain significance	4	74038607	74038607	Human		name
156042744	CV2261482	single nucleotide variant	NM_002090.3(CXCL3):c.11C>G (p.Ala4Gly)	not specified [RCV004130101]	uncertain significance	4	74038601	74038601	Human		name
329375112	CV2431380	single nucleotide variant	NM_002090.3(CXCL3):c.94G>T (p.Ala32Ser)	not specified [RCV004254549]	uncertain significance	4	74038518	74038518	Human		name
329375115	CV2431381	single nucleotide variant	NM_002090.3(CXCL3):c.95C>T (p.Ala32Val)	not specified [RCV004254550]	uncertain significance	4	74038517	74038517	Human		name
598236648	CV3956179	single nucleotide variant	NM_002090.3(CXCL3):c.50G>T (p.Arg17Leu)	not specified [RCV005320478]	uncertain significance	4	74038562	74038562	Human		name
401888764	CV2764660	single nucleotide variant	NM_002090.3(CXCL3):c.188G>A (p.Arg63Lys)	not specified [RCV004341463]	likely benign	4	74038326	74038326	Human		name
405665579	CV3243221	single nucleotide variant	NM_002090.3(CXCL3):c.173A>G (p.Gln58Arg)	not specified [RCV004367574]	uncertain significance	4	74038341	74038341	Human		name
407473325	CV3419968	single nucleotide variant	NM_002090.3(CXCL3):c.125G>A (p.Arg42His)	not specified [RCV004616191]	uncertain significance	4	74038389	74038389	Human		name
597655234	CV3661786	single nucleotide variant	NM_002090.3(CXCL3):c.250G>T (p.Ala84Ser)	not specified [RCV004911027]	uncertain significance	4	74038151	74038151	Human		name
597655243	CV3661787	single nucleotide variant	NM_002090.3(CXCL3):c.191C>T (p.Ser64Phe)	not specified [RCV004911028]	uncertain significance	4	74038323	74038323	Human		name
598236638	CV3956177	single nucleotide variant	NM_002090.3(CXCL3):c.244A>C (p.Lys82Gln)	not specified [RCV005320476]	likely benign	4	74038157	74038157	Human		name
598236644	CV3956178	single nucleotide variant	NM_002090.3(CXCL3):c.106T>C (p.Ser36Pro)	not specified [RCV005320477]	likely benign	4	74038408	74038408	Human		name