Utp18 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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49 records found for search term Utp18

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155997467	CV2250557	single nucleotide variant	NM_016001.3(UTP18):c.11A>G (p.Glu4Gly)	not specified [RCV004129205]	uncertain significance	17	51260595	51260595	Human		name
156022572	CV2223231	single nucleotide variant	NM_016001.3(UTP18):c.66G>T (p.Lys22Asn)	not specified [RCV004104063]	uncertain significance	17	51260650	51260650	Human		name
155919491	CV2360280	single nucleotide variant	NM_016001.3(UTP18):c.47G>A (p.Gly16Glu)	not specified [RCV004208621]	uncertain significance	17	51260631	51260631	Human		name
401769048	CV2686487	single nucleotide variant	NM_016001.3(UTP18):c.94G>A (p.Gly32Arg)	not specified [RCV004290640]	likely benign	17	51260678	51260678	Human		name
407529137	CV3487800	single nucleotide variant	NM_016001.3(UTP18):c.28A>G (p.Lys10Glu)	not specified [RCV004680748]	uncertain significance	17	51260612	51260612	Human		name
156383942	CV2361756	single nucleotide variant	NM_016001.3(UTP18):c.257C>T (p.Ala86Val)	not specified [RCV004223231]	uncertain significance	17	51260841	51260841	Human		name
401885386	CV2768126	single nucleotide variant	NM_016001.3(UTP18):c.230G>A (p.Arg77His)	not specified [RCV004350147]	uncertain significance	17	51260814	51260814	Human		name
405801288	CV3348479	single nucleotide variant	NM_016001.3(UTP18):c.137C>T (p.Ser46Phe)	not specified [RCV004477742]	uncertain significance	17	51260721	51260721	Human		name
405801292	CV3348481	single nucleotide variant	NM_016001.3(UTP18):c.175G>A (p.Ala59Thr)	not specified [RCV004477744]	uncertain significance	17	51260759	51260759	Human		name
407529135	CV3487799	single nucleotide variant	NM_016001.3(UTP18):c.223C>T (p.Arg75Trp)	not specified [RCV004680747]	uncertain significance	17	51260807	51260807	Human		name
597697333	CV3623401	single nucleotide variant	NM_016001.3(UTP18):c.178G>A (p.Ala60Thr)	not specified [RCV004885256]	uncertain significance	17	51260762	51260762	Human		name
598204813	CV3933065	single nucleotide variant	NM_016001.3(UTP18):c.161C>A (p.Pro54Gln)	not specified [RCV005290753]	uncertain significance	17	51260745	51260745	Human		name
598239361	CV3933067	single nucleotide variant	NM_016001.3(UTP18):c.199G>A (p.Glu67Lys)	not specified [RCV005296576]	uncertain significance	17	51260783	51260783	Human		name
156188419	CV2226766	single nucleotide variant	NM_016001.3(UTP18):c.337C>T (p.Pro113Ser)	not specified [RCV004101985]	uncertain significance	17	51260921	51260921	Human		name
156121852	CV2276050	single nucleotide variant	NM_016001.3(UTP18):c.482G>A (p.Arg161Gln)	not specified [RCV004141726]	uncertain significance	17	51266208	51266208	Human		name
156138066	CV2280634	single nucleotide variant	NM_016001.3(UTP18):c.544C>T (p.Leu182Phe)	not specified [RCV004143108]	uncertain significance	17	51266270	51266270	Human		name
155941136	CV2294204	single nucleotide variant	NM_016001.3(UTP18):c.638A>T (p.Asp213Val)	not specified [RCV004149563]	uncertain significance	17	51273377	51273377	Human		name
156390453	CV2373413	single nucleotide variant	NM_016001.3(UTP18):c.638A>G (p.Asp213Gly)	not specified [RCV004220113]	uncertain significance	17	51273377	51273377	Human		name
329357714	CV2427812	single nucleotide variant	NM_016001.3(UTP18):c.364G>C (p.Gly122Arg)	not specified [RCV004252589]	uncertain significance	17	51263295	51263295	Human		name
401728893	CV2673082	single nucleotide variant	NM_016001.3(UTP18):c.757C>T (p.Arg253Trp)	not specified [RCV004284069]	uncertain significance	17	51275911	51275911	Human		name
401766899	CV2680186	single nucleotide variant	NM_016001.3(UTP18):c.968A>G (p.Tyr323Cys)	not specified [RCV004286665]	uncertain significance	17	51277260	51277260	Human		name
401760766	CV2706086	single nucleotide variant	NM_016001.3(UTP18):c.688T>A (p.Ser230Thr)	not specified [RCV004314777]	uncertain significance	17	51273427	51273427	Human		name
405801294	CV3348482	single nucleotide variant	NM_016001.3(UTP18):c.466A>G (p.Met156Val)	not specified [RCV004477745]	uncertain significance	17	51266192	51266192	Human		name
405801295	CV3348483	single nucleotide variant	NM_016001.3(UTP18):c.604C>T (p.Arg202Trp)	not specified [RCV004477746]	uncertain significance	17	51268886	51268886	Human		name
405801297	CV3348484	single nucleotide variant	NM_016001.3(UTP18):c.911G>A (p.Ser304Asn)	not specified [RCV004477747]	uncertain significance	17	51277203	51277203	Human		name
407529133	CV3487798	single nucleotide variant	NM_016001.3(UTP18):c.406C>T (p.Pro136Ser)	not specified [RCV004680746]	uncertain significance	17	51263337	51263337	Human		name
597799335	CV3623397	single nucleotide variant	NM_016001.3(UTP18):c.304G>A (p.Asp102Asn)	not specified [RCV004879626]	uncertain significance	17	51260888	51260888	Human		name
597799337	CV3623398	single nucleotide variant	NM_016001.3(UTP18):c.853A>G (p.Asn285Asp)	not specified [RCV004879627]	uncertain significance	17	51277145	51277145	Human		name
597697324	CV3623399	single nucleotide variant	NM_016001.3(UTP18):c.561A>C (p.Gln187His)	not specified [RCV004885255]	uncertain significance	17	51268843	51268843	Human		name
597799339	CV3623400	single nucleotide variant	NM_016001.3(UTP18):c.774G>T (p.Gln258His)	not specified [RCV004879628]	uncertain significance	17	51275928	51275928	Human		name
597799345	CV3623405	single nucleotide variant	NM_016001.3(UTP18):c.719A>G (p.Asn240Ser)	not specified [RCV004879631]	uncertain significance	17	51275873	51275873	Human		name
598239355	CV3933066	single nucleotide variant	NM_016001.3(UTP18):c.338C>G (p.Pro113Arg)	not specified [RCV005296575]	uncertain significance	17	51260922	51260922	Human		name
598239368	CV3933068	single nucleotide variant	NM_016001.3(UTP18):c.482G>C (p.Arg161Pro)	not specified [RCV005296577]	uncertain significance	17	51266208	51266208	Human		name
598204818	CV3933069	single nucleotide variant	NM_016001.3(UTP18):c.890C>T (p.Pro297Leu)	not specified [RCV005290754]	uncertain significance	17	51277182	51277182	Human		name
598239374	CV3933070	single nucleotide variant	NM_016001.3(UTP18):c.317T>C (p.Leu106Ser)	not specified [RCV005296578]	uncertain significance	17	51260901	51260901	Human		name
8636247	CV91471	single nucleotide variant	NM_016001.2(UTP18):c.403C>T (p.Pro135Ser)	Malignant melanoma [RCV000071569]	not provided	17	51263334	51263334	Human		name
156175684	CV2205264	single nucleotide variant	NM_016001.3(UTP18):c.1534A>G (p.Asn512Asp)	not specified [RCV004079889]	uncertain significance	17	51293933	51293933	Human		name
156179326	CV2229536	single nucleotide variant	NM_016001.3(UTP18):c.1105G>A (p.Ala369Thr)	not specified [RCV004103074]	uncertain significance	17	51280097	51280097	Human		name
156213220	CV2257355	single nucleotide variant	NM_016001.3(UTP18):c.1502T>G (p.Leu501Trp)	not specified [RCV004125447]	uncertain significance	17	51288202	51288202	Human		name
156038996	CV2261174	single nucleotide variant	NM_016001.3(UTP18):c.1287A>C (p.Leu429Phe)	not specified [RCV004128064]	uncertain significance	17	51285327	51285327	Human		name
156368613	CV2267043	single nucleotide variant	NM_016001.3(UTP18):c.1403C>G (p.Ala468Gly)	not specified [RCV004131680]	uncertain significance	17	51288103	51288103	Human		name
156260244	CV2381111	single nucleotide variant	NM_016001.3(UTP18):c.1280A>G (p.Tyr427Cys)	not specified [RCV004225143]	uncertain significance	17	51285320	51285320	Human		name
329386667	CV2428373	single nucleotide variant	NM_016001.3(UTP18):c.1654C>T (p.His552Tyr)	not specified [RCV004253181]	uncertain significance	17	51296972	51296972	Human		name
401719229	CV2705014	single nucleotide variant	NM_016001.3(UTP18):c.1144A>G (p.Asn382Asp)	not specified [RCV004309612]	uncertain significance	17	51280419	51280419	Human		name
401892158	CV2775972	single nucleotide variant	NM_016001.3(UTP18):c.1514C>T (p.Pro505Leu)	not specified [RCV004344988]	uncertain significance	17	51293913	51293913	Human		name
405801468	CV3348477	single nucleotide variant	NM_016001.3(UTP18):c.1007T>C (p.Val336Ala)	not specified [RCV004477740]	uncertain significance	17	51277299	51277299	Human		name
405801286	CV3348478	single nucleotide variant	NM_016001.3(UTP18):c.1153G>A (p.Val385Ile)	not specified [RCV004477741]	likely benign	17	51280428	51280428	Human		name
407529141	CV3487802	single nucleotide variant	NM_016001.3(UTP18):c.1445A>G (p.Asn482Ser)	not specified [RCV004680750]	uncertain significance	17	51288145	51288145	Human		name
598239379	CV3933073	single nucleotide variant	NM_016001.3(UTP18):c.1230T>G (p.Asp410Glu)	not specified [RCV005296579]	uncertain significance	17	51285270	51285270	Human		name

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