Zscan18 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

56 records found for search term Zscan18

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156077044	CV2375078	single nucleotide variant	NM_001145543.2(ZSCAN18):c.-11G>A	not specified [RCV004230126]	uncertain significance	19	58090278	58090278	Human		name
8637095	CV92321	single nucleotide variant	NM_001145542.1(ZSCAN18):c.721+37C>T	Malignant melanoma [RCV000072419]	not provided	19	58088651	58088651	Human		name
156182733	CV2243118	single nucleotide variant	NM_001145543.2(ZSCAN18):c.50C>T (p.Pro17Leu)	not specified [RCV004110027]	uncertain significance	19	58090218	58090218	Human		name
156166381	CV2330127	single nucleotide variant	NM_001145543.2(ZSCAN18):c.39C>G (p.Ser13Arg)	not specified [RCV004185617]	uncertain significance	19	58090229	58090229	Human		name
156350631	CV2316242	single nucleotide variant	NM_001145543.2(ZSCAN18):c.146G>A (p.Arg49His)	not specified [RCV004174275]	uncertain significance	19	58090122	58090122	Human		name
405676227	CV3355062	single nucleotide variant	NM_001145543.2(ZSCAN18):c.184G>A (p.Gly62Arg)	not specified [RCV004487689]	uncertain significance	19	58090084	58090084	Human		name
597748573	CV3646232	single nucleotide variant	NM_001145543.2(ZSCAN18):c.101C>T (p.Pro34Leu)	not specified [RCV004892152]	uncertain significance	19	58090167	58090167	Human		name
156073091	CV2325403	single nucleotide variant	NM_001145543.2(ZSCAN18):c.824G>A (p.Gly275Glu)	not specified [RCV004177768]	uncertain significance	19	58086188	58086188	Human		name
156186225	CV2332509	single nucleotide variant	NM_001145543.2(ZSCAN18):c.881A>C (p.Glu294Ala)	not specified [RCV004196230]	uncertain significance	19	58085337	58085337	Human		name
156037109	CV2332510	single nucleotide variant	NM_001145543.2(ZSCAN18):c.882G>C (p.Glu294Asp)	not specified [RCV004196231]	uncertain significance	19	58085336	58085336	Human		name
156089665	CV2344469	single nucleotide variant	NM_001145543.2(ZSCAN18):c.950C>G (p.Pro317Arg)	not specified [RCV004195213]	uncertain significance	19	58085268	58085268	Human		name
156216291	CV2347974	single nucleotide variant	NM_001145543.2(ZSCAN18):c.662A>T (p.Glu221Val)	not specified [RCV004197661]	uncertain significance	19	58086989	58086989	Human		name
329360306	CV2446667	single nucleotide variant	NM_001145543.2(ZSCAN18):c.536C>T (p.Pro179Leu)	not specified [RCV004251553]	uncertain significance	19	58088705	58088705	Human		name
329395864	CV2454661	single nucleotide variant	NM_001145543.2(ZSCAN18):c.994G>T (p.Ala332Ser)	not specified [RCV004268119]	uncertain significance	19	58085224	58085224	Human		name
401743605	CV2684744	single nucleotide variant	NM_001145543.2(ZSCAN18):c.800G>A (p.Arg267Gln)	not specified [RCV004293832]	likely benign	19	58086212	58086212	Human		name
405676193	CV3355055	single nucleotide variant	NM_001145543.2(ZSCAN18):c.948T>A (p.Asp316Glu)	not specified [RCV004487682]	uncertain significance	19	58085270	58085270	Human		name
405676198	CV3355056	single nucleotide variant	NM_001145543.2(ZSCAN18):c.956C>T (p.Ser319Leu)	not specified [RCV004487683]	uncertain significance	19	58085262	58085262	Human		name
405676233	CV3355063	single nucleotide variant	NM_001145543.2(ZSCAN18):c.353A>G (p.Lys118Arg)	not specified [RCV004487690]	uncertain significance	19	58089915	58089915	Human		name
405676239	CV3355064	single nucleotide variant	NM_001145543.2(ZSCAN18):c.509G>A (p.Ser170Asn)	not specified [RCV004487691]	uncertain significance	19	58088732	58088732	Human		name
405676244	CV3355065	single nucleotide variant	NM_001145543.2(ZSCAN18):c.566C>T (p.Pro189Leu)	not specified [RCV004487692]	likely benign	19	58087392	58087392	Human		name
407487728	CV3421010	single nucleotide variant	NM_001145543.2(ZSCAN18):c.471G>A (p.Met157Ile)	not specified [RCV004603826]	uncertain significance	19	58088770	58088770	Human		name
597748555	CV3646228	single nucleotide variant	NM_001145543.2(ZSCAN18):c.609G>C (p.Lys203Asn)	not specified [RCV004892148]	uncertain significance	19	58087349	58087349	Human		name
597748564	CV3646230	single nucleotide variant	NM_001145543.2(ZSCAN18):c.937G>A (p.Ala313Thr)	not specified [RCV004892150]	uncertain significance	19	58085281	58085281	Human		name
597748568	CV3646231	single nucleotide variant	NM_001145543.2(ZSCAN18):c.976G>A (p.Glu326Lys)	not specified [RCV004892151]	uncertain significance	19	58085242	58085242	Human		name
597748576	CV3646233	single nucleotide variant	NM_001145543.2(ZSCAN18):c.907G>C (p.Glu303Gln)	not specified [RCV004892153]	uncertain significance	19	58085311	58085311	Human		name
597748586	CV3646235	single nucleotide variant	NM_001145543.2(ZSCAN18):c.452G>C (p.Gly151Ala)	not specified [RCV004892155]	uncertain significance	19	58088789	58088789	Human		name
598200749	CV3942196	single nucleotide variant	NM_001145543.2(ZSCAN18):c.955T>C (p.Ser319Pro)	not specified [RCV005314110]	uncertain significance	19	58085263	58085263	Human		name
598276385	CV3942197	single nucleotide variant	NM_001145543.2(ZSCAN18):c.503G>T (p.Ser168Ile)	not specified [RCV005305519]	uncertain significance	19	58088738	58088738	Human		name
155917664	CV2199048	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1250A>T (p.Glu417Val)	not specified [RCV004080450]	uncertain significance	19	58084968	58084968	Human		name
156229106	CV2199461	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1165G>A (p.Gly389Ser)	not specified [RCV004071019]	likely benign	19	58085053	58085053	Human		name
156236740	CV2235599	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1408G>A (p.Ala470Thr)	not specified [RCV004111754]	uncertain significance	19	58084810	58084810	Human		name
155973936	CV2235600	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1409C>A (p.Ala470Glu)	not specified [RCV004111755]	uncertain significance	19	58084809	58084809	Human		name
156156156	CV2238379	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1334G>A (p.Gly445Asp)	not specified [RCV004113449]	uncertain significance	19	58084884	58084884	Human		name
156195297	CV2251833	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1083C>G (p.Asp361Glu)	not specified [RCV004119821]	uncertain significance	19	58085135	58085135	Human		name
155989008	CV2285547	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1396G>A (p.Glu466Lys)	not specified [RCV004141425]	uncertain significance	19	58084822	58084822	Human		name
156279082	CV2297586	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1298G>A (p.Ser433Asn)	not specified [RCV004155288]	uncertain significance	19	58084920	58084920	Human		name
156072519	CV2328796	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1324G>A (p.Ala442Thr)	not specified [RCV004178021]	uncertain significance	19	58084894	58084894	Human		name
156341451	CV2368411	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1157C>G (p.Ser386Cys)	not specified [RCV004219179]	uncertain significance	19	58085061	58085061	Human		name
155907004	CV2379189	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1489G>A (p.Val497Met)	not specified [RCV004235977]	uncertain significance	19	58084729	58084729	Human		name
401889461	CV2756597	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1393A>G (p.Lys465Glu)	not specified [RCV004345120]	uncertain significance	19	58084825	58084825	Human		name
401855389	CV2757299	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1096A>C (p.Lys366Gln)	not specified [RCV004338887]	uncertain significance	19	58085122	58085122	Human		name
401896044	CV2777312	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1486A>G (p.Ser496Gly)	not specified [RCV004354327]	uncertain significance	19	58084732	58084732	Human		name
405676203	CV3355057	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1124A>T (p.Glu375Val)	not specified [RCV004487684]	uncertain significance	19	58085094	58085094	Human		name
405676208	CV3355058	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1204G>C (p.Ala402Pro)	not specified [RCV004487685]	uncertain significance	19	58085014	58085014	Human		name
405676213	CV3355059	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1209C>A (p.Asp403Glu)	not specified [RCV004487686]	uncertain significance	19	58085009	58085009	Human		name
405676218	CV3355060	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1241C>T (p.Ala414Val)	not specified [RCV004487687]	uncertain significance	19	58084977	58084977	Human		name
405676223	CV3355061	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1456G>T (p.Ala486Ser)	not specified [RCV004487688]	uncertain significance	19	58084762	58084762	Human		name
407487724	CV3421008	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1294C>T (p.His432Tyr)	not specified [RCV004603825]	uncertain significance	19	58084924	58084924	Human		name
407499680	CV3421009	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1032C>A (p.Asp344Glu)	not specified [RCV004606935]	uncertain significance	19	58085186	58085186	Human		name
407487733	CV3421011	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1478C>T (p.Pro493Leu)	not specified [RCV004603827]	uncertain significance	19	58084740	58084740	Human		name
597748550	CV3646227	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1096A>G (p.Lys366Glu)	not specified [RCV004892147]	uncertain significance	19	58085122	58085122	Human		name
597748559	CV3646229	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1297A>G (p.Ser433Gly)	not specified [RCV004892149]	uncertain significance	19	58084921	58084921	Human		name
597748581	CV3646234	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1004C>T (p.Pro335Leu)	not specified [RCV004892154]	uncertain significance	19	58085214	58085214	Human		name
597748590	CV3646236	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1033T>C (p.Ser345Pro)	not specified [RCV004892156]	likely benign	19	58085185	58085185	Human		name
597748595	CV3646237	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1036G>A (p.Ala346Thr)	not specified [RCV004892157]	uncertain significance	19	58085182	58085182	Human		name
598276384	CV3942195	single nucleotide variant	NM_001145543.2(ZSCAN18):c.1312C>T (p.Arg438Trp)	not specified [RCV005305518]	uncertain significance	19	58084906	58084906	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message