St3gal4 Variant Search Result - Rat Genome Database

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31 records found for search term St3gal4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8652669	CV129244	single nucleotide variant	NM_001254757.1(ST3GAL4):c.-61+7149C>T	Lung cancer [RCV000109731]	uncertain significance	11	126362991	126362991	Human		name
11551031	CV254057	single nucleotide variant	NM_001254757.2(ST3GAL4):c.252C>T (p.Tyr84=)	not provided [RCV004706700]\|not specified [RCV000252516]	benign	11	126407321	126407321	Human	2	name
11551031	CV254057	single nucleotide variant	NM_001254757.2(ST3GAL4):c.252C>T (p.Tyr84=)	not provided [RCV004706700]\|not specified [RCV000252516]	benign	11	126407321	126407322	Human	2	name
155921083	CV2350610	single nucleotide variant	NM_001254757.2(ST3GAL4):c.80G>A (p.Arg27Gln)	not specified [RCV004204953]	uncertain significance	11	126406536	126406536	Human		name
156226300	CV2352730	single nucleotide variant	NM_001254757.2(ST3GAL4):c.43C>G (p.Leu15Val)	not specified [RCV004198752]	uncertain significance	11	126406499	126406499	Human		name
11542969	CV254058	single nucleotide variant	NM_001254757.2(ST3GAL4):c.423C>T (p.Tyr141=)	not provided [RCV004706701]\|not specified [RCV000241833]	benign	11	126408180	126408180	Human		name
11546558	CV254059	single nucleotide variant	NM_001254757.2(ST3GAL4):c.439T>C (p.Leu147=)	not provided [RCV004706702]\|not specified [RCV000246620]	benign	11	126408308	126408308	Human	24	name
407517234	CV3475074	single nucleotide variant	NM_001254757.2(ST3GAL4):c.46G>T (p.Val16Phe)	not specified [RCV004675574]	uncertain significance	11	126406502	126406502	Human		name
156181752	CV2338149	single nucleotide variant	NM_001254757.2(ST3GAL4):c.134C>T (p.Pro45Leu)	not specified [RCV004184180]	uncertain significance	11	126406975	126406975	Human		name
329351631	CV2459204	single nucleotide variant	NM_001254757.2(ST3GAL4):c.110T>C (p.Phe37Ser)	not specified [RCV004272646]	uncertain significance	11	126406951	126406951	Human		name
401727845	CV2678510	single nucleotide variant	NM_001254757.2(ST3GAL4):c.191G>A (p.Arg64Gln)	not specified [RCV004292524]	uncertain significance	11	126407260	126407260	Human		name
401856313	CV2754598	single nucleotide variant	NM_001254757.2(ST3GAL4):c.239C>T (p.Thr80Met)	not specified [RCV004339275]	uncertain significance	11	126407308	126407308	Human		name
405720329	CV3323442	single nucleotide variant	NM_001254757.2(ST3GAL4):c.121G>A (p.Glu41Lys)	not specified [RCV004463043]	uncertain significance	11	126406962	126406962	Human		name
405720337	CV3323443	single nucleotide variant	NM_001254757.2(ST3GAL4):c.235A>G (p.Lys79Glu)	not specified [RCV004463044]	uncertain significance	11	126407304	126407304	Human		name
407517228	CV3475072	single nucleotide variant	NM_001254757.2(ST3GAL4):c.160A>C (p.Lys54Gln)	not specified [RCV004675572]	uncertain significance	11	126407001	126407001	Human		name
407517231	CV3475073	single nucleotide variant	NM_001254757.2(ST3GAL4):c.157A>C (p.Ser53Arg)	not specified [RCV004675573]	likely benign	11	126406998	126406998	Human		name
597745931	CV3608591	single nucleotide variant	NM_001254757.2(ST3GAL4):c.190C>T (p.Arg64Trp)	not specified [RCV004865762]	uncertain significance	11	126407259	126407259	Human		name
598175512	CV3923079	single nucleotide variant	NM_001254757.2(ST3GAL4):c.134C>A (p.Pro45Gln)	not specified [RCV005285501]	uncertain significance	11	126406975	126406975	Human		name
598175529	CV3923082	single nucleotide variant	NM_001254757.2(ST3GAL4):c.292C>T (p.Leu98Phe)	not specified [RCV005285503]	uncertain significance	11	126407585	126407585	Human		name
598175544	CV3923084	single nucleotide variant	NM_001254757.2(ST3GAL4):c.253G>A (p.Glu85Lys)	not specified [RCV005285505]	uncertain significance	11	126407322	126407322	Human		name
156035108	CV2208055	single nucleotide variant	NM_001254757.2(ST3GAL4):c.389G>A (p.Arg130Gln)	not specified [RCV004086747]	uncertain significance	11	126408146	126408146	Human		name
401718226	CV2700244	single nucleotide variant	NM_001254757.2(ST3GAL4):c.355C>T (p.Arg119Cys)	not specified [RCV004310912]	uncertain significance	11	126408112	126408112	Human		name
405720344	CV3323444	single nucleotide variant	NM_001254757.2(ST3GAL4):c.598A>G (p.Ile200Val)	not specified [RCV004463045]	uncertain significance	11	126408467	126408467	Human		name
405720351	CV3323445	single nucleotide variant	NM_001254757.2(ST3GAL4):c.674A>G (p.Asn225Ser)	not specified [RCV004463046]	uncertain significance	11	126409314	126409314	Human		name
597745935	CV3608592	single nucleotide variant	NM_001254757.2(ST3GAL4):c.632G>A (p.Arg211Gln)	not specified [RCV004865763]	uncertain significance	11	126409272	126409272	Human		name
597745940	CV3608593	single nucleotide variant	NM_001254757.2(ST3GAL4):c.388C>T (p.Arg130Trp)	not specified [RCV004865764]	uncertain significance	11	126408145	126408145	Human		name
598175506	CV3923078	single nucleotide variant	NM_001254757.2(ST3GAL4):c.623A>C (p.Lys208Thr)	not specified [RCV005285500]	uncertain significance	11	126408492	126408492	Human		name
598213992	CV3923080	single nucleotide variant	NM_001254757.2(ST3GAL4):c.910A>G (p.Met304Val)	not specified [RCV005271068]	uncertain significance	11	126413643	126413643	Human		name
598175519	CV3923081	single nucleotide variant	NM_001254757.2(ST3GAL4):c.562G>A (p.Val188Ile)	not specified [RCV005285502]	uncertain significance	11	126408431	126408431	Human		name
598175537	CV3923083	single nucleotide variant	NM_001254757.2(ST3GAL4):c.469G>A (p.Gly157Ser)	not specified [RCV005285504]	uncertain significance	11	126408338	126408338	Human		name
598175551	CV3923085	single nucleotide variant	NM_001254757.2(ST3GAL4):c.988C>A (p.Leu330Ile)	not specified [RCV005285506]	uncertain significance	11	126414033	126414033	Human		name

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