Pop4 Variant Search Result - Rat Genome Database

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26 records found for search term Pop4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405668431	CV3369810	single nucleotide variant	NM_006627.3(POP4):c.8G>A (p.Ser3Asn)	not specified [RCV004514646]	uncertain significance	19	29608657	29608657	Human		name
407482161	CV3461097	single nucleotide variant	NM_006627.3(POP4):c.80C>A (p.Ala27Asp)	not specified [RCV004664717]	uncertain significance	19	29610428	29610428	Human		name
155931788	CV2293698	single nucleotide variant	NM_006627.3(POP4):c.207G>T (p.Lys69Asn)	not specified [RCV004154989]	uncertain significance	19	29610555	29610555	Human		name
156096562	CV2310193	single nucleotide variant	NM_006627.3(POP4):c.158G>T (p.Arg53Leu)	not specified [RCV004163298]	uncertain significance	19	29610506	29610506	Human		name
329369129	CV2424734	single nucleotide variant	NM_006627.3(POP4):c.122G>A (p.Arg41His)	not specified [RCV004248628]	likely benign	19	29610470	29610470	Human		name
401780423	CV2674018	single nucleotide variant	NM_006627.3(POP4):c.116C>T (p.Thr39Met)	not specified [RCV004293383]	likely benign	19	29610464	29610464	Human		name
405668421	CV3369808	single nucleotide variant	NM_006627.3(POP4):c.116C>G (p.Thr39Arg)	not specified [RCV004514644]	uncertain significance	19	29610464	29610464	Human		name
405668426	CV3369809	single nucleotide variant	NM_006627.3(POP4):c.239A>C (p.Gln80Pro)	not specified [RCV004514645]	uncertain significance	19	29610587	29610587	Human		name
407525231	CV3461096	single nucleotide variant	NM_006627.3(POP4):c.254G>A (p.Arg85Gln)	not specified [RCV004653987]	uncertain significance	19	29610602	29610602	Human		name
407525219	CV3461098	single nucleotide variant	NM_006627.3(POP4):c.238C>G (p.Gln80Glu)	not specified [RCV004653988]	uncertain significance	19	29610586	29610586	Human		name
597778532	CV3580790	single nucleotide variant	NM_006627.3(POP4):c.185C>T (p.Thr62Ile)	not specified [RCV004853029]	uncertain significance	19	29610533	29610533	Human		name
597778857	CV3580796	single nucleotide variant	NM_006627.3(POP4):c.181T>G (p.Phe61Val)	not specified [RCV004853034]	uncertain significance	19	29610529	29610529	Human		name
598159036	CV3900933	single nucleotide variant	NM_006627.3(POP4):c.145G>A (p.Asp49Asn)	not specified [RCV005260620]	uncertain significance	19	29610493	29610493	Human		name
598159046	CV3900935	single nucleotide variant	NM_006627.3(POP4):c.118C>T (p.Pro40Ser)	not specified [RCV005260622]	uncertain significance	19	29610466	29610466	Human		name
156054084	CV2308639	single nucleotide variant	NM_006627.3(POP4):c.619C>T (p.Arg207Trp)	not specified [RCV004167193]	uncertain significance	19	29615336	29615336	Human		name
156065715	CV2348896	single nucleotide variant	NM_006627.3(POP4):c.529A>T (p.Ile177Phe)	not specified [RCV004203332]	likely benign	19	29615246	29615246	Human		name
329378001	CV2436105	single nucleotide variant	NM_006627.3(POP4):c.328A>C (p.Ile110Leu)	not specified [RCV004249351]	uncertain significance	19	29611905	29611905	Human		name
329398222	CV2464307	single nucleotide variant	NM_006627.3(POP4):c.409G>A (p.Gly137Arg)	not specified [RCV004276263]	uncertain significance	19	29612163	29612163	Human		name
329353508	CV2466796	single nucleotide variant	NM_006627.3(POP4):c.620G>A (p.Arg207Gln)	not specified [RCV004280744]	uncertain significance	19	29615337	29615337	Human		name
401872693	CV2764294	single nucleotide variant	NM_006627.3(POP4):c.646G>A (p.Gly216Arg)	not specified [RCV004336826]	uncertain significance	19	29615363	29615363	Human		name
597778527	CV3580789	single nucleotide variant	NM_006627.3(POP4):c.401A>T (p.Asp134Val)	not specified [RCV004853028]	uncertain significance	19	29612155	29612155	Human		name
597778534	CV3580791	single nucleotide variant	NM_006627.3(POP4):c.638A>C (p.Lys213Thr)	not specified [RCV004853030]	uncertain significance	19	29615355	29615355	Human		name
597778538	CV3580792	single nucleotide variant	NM_006627.3(POP4):c.647G>T (p.Gly216Val)	not specified [RCV004853031]	uncertain significance	19	29615364	29615364	Human		name
597778546	CV3580795	single nucleotide variant	NM_006627.3(POP4):c.319A>G (p.Lys107Glu)	not specified [RCV004853033]	uncertain significance	19	29611896	29611896	Human		name
598159030	CV3900932	single nucleotide variant	NM_006627.3(POP4):c.608G>A (p.Arg203Gln)	not specified [RCV005260619]	uncertain significance	19	29615325	29615325	Human		name
598159041	CV3900934	single nucleotide variant	NM_006627.3(POP4):c.608G>C (p.Arg203Pro)	not specified [RCV005260621]	uncertain significance	19	29615325	29615325	Human		name

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