Zscan18 Variant Search Result - Rat Genome Database

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56 records found for search term Zscan18

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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

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