Mapk11 Variant Search Result - Rat Genome Database

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20 records found for search term Mapk11

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15171134	CV731435	single nucleotide variant	NM_002751.7(MAPK11):c.611-7C>T	not provided [RCV000883598]	benign	22	50266618	50266618	Human		name
401922012	CV2819751	single nucleotide variant	NM_002751.7(MAPK11):c.882C>T (p.Asp294=)	not provided [RCV003433335]	likely benign	22	50265454	50265454	Human		name
407494326	CV3446655	single nucleotide variant	NM_002751.7(MAPK11):c.306G>A (p.Val102=)	not specified [RCV004642966]	likely benign	22	50267482	50267482	Human		name
156250976	CV2232245	single nucleotide variant	NM_002751.7(MAPK11):c.229C>T (p.His77Tyr)	not specified [RCV004105030]	uncertain significance	22	50267837	50267837	Human		name
401757193	CV2692855	single nucleotide variant	NM_002751.7(MAPK11):c.133C>T (p.Arg45Trp)	not specified [RCV004306391]	uncertain significance	22	50267933	50267933	Human		name
156125676	CV2237645	single nucleotide variant	NM_002751.7(MAPK11):c.637A>G (p.Met213Val)	not specified [RCV004106574]	uncertain significance	22	50266585	50266585	Human		name
156135679	CV2245619	single nucleotide variant	NM_002751.7(MAPK11):c.793A>C (p.Met265Leu)	not specified [RCV004111512]	uncertain significance	22	50265630	50265630	Human		name
156107864	CV2390180	single nucleotide variant	NM_002751.7(MAPK11):c.940C>T (p.Pro314Ser)	not specified [RCV004240563]	uncertain significance	22	50265396	50265396	Human		name
329388528	CV2469360	single nucleotide variant	NM_002751.7(MAPK11):c.755C>T (p.Ser252Leu)	not specified [RCV004280998]	uncertain significance	22	50266233	50266233	Human		name
401746701	CV2690951	single nucleotide variant	NM_002751.7(MAPK11):c.975G>C (p.Glu325Asp)	not specified [RCV004300976]	uncertain significance	22	50265361	50265361	Human		name
401760116	CV2694928	single nucleotide variant	NM_002751.7(MAPK11):c.995G>A (p.Arg332His)	not specified [RCV004301317]	uncertain significance	22	50265341	50265341	Human		name
405811674	CV3285054	single nucleotide variant	NM_002751.7(MAPK11):c.481G>A (p.Asp161Asn)	not specified [RCV004408590]	uncertain significance	22	50267141	50267141	Human		name
405811676	CV3285055	single nucleotide variant	NM_002751.7(MAPK11):c.541G>A (p.Gly181Ser)	not specified [RCV004408591]	uncertain significance	22	50267003	50267003	Human		name
405811678	CV3285056	single nucleotide variant	NM_002751.7(MAPK11):c.671C>G (p.Pro224Arg)	not specified [RCV004408592]	uncertain significance	22	50266551	50266551	Human		name
407469148	CV3446656	single nucleotide variant	NM_002751.7(MAPK11):c.910G>T (p.Ala304Ser)	not specified [RCV004636527]	uncertain significance	22	50265426	50265426	Human		name
598176502	CV3985305	single nucleotide variant	NM_002751.7(MAPK11):c.845T>C (p.Ile282Thr)	not specified [RCV005371424]	uncertain significance	22	50265491	50265491	Human		name
598198112	CV3985306	single nucleotide variant	NM_002751.7(MAPK11):c.484T>C (p.Cys162Arg)	not specified [RCV005375508]	uncertain significance	22	50267138	50267138	Human		name
156274930	CV2279868	single nucleotide variant	NM_002751.7(MAPK11):c.1048C>T (p.Pro350Ser)	not specified [RCV004144462]	uncertain significance	22	50264995	50264995	Human		name
156194126	CV2322063	single nucleotide variant	NM_002751.7(MAPK11):c.1008G>C (p.Glu336Asp)	not specified [RCV004173807]	uncertain significance	22	50265328	50265328	Human		name
405811672	CV3285053	single nucleotide variant	NM_002751.7(MAPK11):c.1060C>G (p.Pro354Ala)	not specified [RCV004408589]	uncertain significance	22	50264983	50264983	Human		name

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