Spcs2 Variant Search Result - Rat Genome Database

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13 records found for search term Spcs2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405716747	CV3326656	single nucleotide variant	NM_014752.3(SPCS2):c.40A>G (p.Ser14Gly)	not specified [RCV004462607]	likely benign	11	74949325	74949325	Human		name
597767941	CV3608110	single nucleotide variant	NM_014752.3(SPCS2):c.47G>T (p.Gly16Val)	not specified [RCV004870934]	uncertain significance	11	74949332	74949332	Human		name
401868402	CV2781261	single nucleotide variant	NM_014752.3(SPCS2):c.194A>G (p.Lys65Arg)	not specified [RCV004352294]	uncertain significance	11	74965113	74965113	Human		name
405716737	CV3326655	single nucleotide variant	NM_014752.3(SPCS2):c.284C>G (p.Ala95Gly)	not specified [RCV004462606]	uncertain significance	11	74965848	74965848	Human		name
407525569	CV3481619	single nucleotide variant	NM_014752.3(SPCS2):c.148A>G (p.Lys50Glu)	not specified [RCV004679320]	uncertain significance	11	74965067	74965067	Human		name
597767951	CV3608113	single nucleotide variant	NM_014752.3(SPCS2):c.278T>C (p.Phe93Ser)	not specified [RCV004870936]	uncertain significance	11	74965842	74965842	Human		name
329377302	CV2442726	single nucleotide variant	NM_014752.3(SPCS2):c.563A>G (p.Glu188Gly)	not specified [RCV004266859]	uncertain significance	11	74976925	74976925	Human		name
329392108	CV2470384	single nucleotide variant	NM_014752.3(SPCS2):c.412A>G (p.Ser138Gly)	not specified [RCV004273421]	uncertain significance	11	74969617	74969617	Human		name
401734920	CV2706585	single nucleotide variant	NM_014752.3(SPCS2):c.551A>G (p.Gln184Arg)	not specified [RCV004319170]	uncertain significance	11	74976913	74976913	Human		name
401769992	CV2710794	single nucleotide variant	NM_014752.3(SPCS2):c.372G>T (p.Met124Ile)	not specified [RCV004308723]	uncertain significance	11	74969577	74969577	Human		name
407525567	CV3481618	single nucleotide variant	NM_014752.3(SPCS2):c.620C>T (p.Ala207Val)	not specified [RCV004679319]	uncertain significance	11	74976982	74976982	Human		name
597742646	CV3608111	single nucleotide variant	NM_014752.3(SPCS2):c.337G>A (p.Val113Ile)	not specified [RCV004865123]	uncertain significance	11	74965901	74965901	Human		name
597767946	CV3608112	single nucleotide variant	NM_014752.3(SPCS2):c.596A>G (p.His199Arg)	not specified [RCV004870935]	uncertain significance	11	74976958	74976958	Human		name