Usp47 Variant Search Result - Rat Genome Database

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83 records found for search term Usp47

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8626918	CV82062	single nucleotide variant	NM_017944.3(USP47):c.2887+16G>A	Malignant melanoma [RCV000062141]	not provided	11	11943128	11943128	Human		name
401909418	CV2816453	single nucleotide variant	NM_001282659.2(USP47):c.3583+5T>A	not provided [RCV003397930]	likely benign	11	11950487	11950487	Human		name
8652606	CV129181	single nucleotide variant	NM_001282659.1(USP47):c.1387-1922A>G	Lung cancer [RCV000109668]	uncertain significance	11	11927512	11927512	Human		name
401909417	CV2816452	single nucleotide variant	NM_001282659.2(USP47):c.309C>T (p.Asn103=)	not provided [RCV003397929]	likely benign	11	11884532	11884532	Human		name
401889473	CV2756612	single nucleotide variant	NM_001282659.2(USP47):c.283G>A (p.Ala95Thr)	not specified [RCV004345134]	uncertain significance	11	11884506	11884506	Human		name
405800984	CV3338358	single nucleotide variant	NM_001282659.2(USP47):c.286A>C (p.Asn96His)	not specified [RCV004477557]	uncertain significance	11	11884509	11884509	Human		name
156193100	CV2296928	single nucleotide variant	NM_001282659.2(USP47):c.439A>G (p.Ser147Gly)	not specified [RCV004149076]	uncertain significance	11	11892049	11892049	Human		name
156180988	CV2327783	single nucleotide variant	NM_001282659.2(USP47):c.394A>G (p.Arg132Gly)	not specified [RCV004179128]	uncertain significance	11	11892004	11892004	Human		name
401877652	CV2761248	single nucleotide variant	NM_001282659.2(USP47):c.712A>G (p.Arg238Gly)	not specified [RCV004341125]	uncertain significance	11	11902833	11902833	Human		name
401876477	CV2767602	single nucleotide variant	NM_001282659.2(USP47):c.691A>G (p.Ile231Val)	not specified [RCV004343747]	uncertain significance	11	11902812	11902812	Human		name
405800917	CV3338347	single nucleotide variant	NM_001282659.2(USP47):c.448G>A (p.Val150Ile)	not specified [RCV004477546]	uncertain significance	11	11892058	11892058	Human		name
15184039	CV737805	single nucleotide variant	NM_001282659.2(USP47):c.3330T>G (p.Leu1110=)	not provided [RCV000908189]	benign	11	11948540	11948540	Human		name
156324266	CV2198627	single nucleotide variant	NM_001282659.2(USP47):c.1291A>G (p.Ser431Gly)	not specified [RCV004075643]	uncertain significance	11	11922796	11922796	Human		name
156244540	CV2207296	single nucleotide variant	NM_001282659.2(USP47):c.1061G>A (p.Arg354Gln)	not specified [RCV004088010]	uncertain significance	11	11920247	11920247	Human		name
155982232	CV2208709	single nucleotide variant	NM_001282659.2(USP47):c.2150A>G (p.Tyr717Cys)	not specified [RCV004084900]	uncertain significance	11	11938329	11938329	Human		name
155971364	CV2242905	single nucleotide variant	NM_001282659.2(USP47):c.1255G>A (p.Ala419Thr)	not specified [RCV004107494]	uncertain significance	11	11922760	11922760	Human		name
155998618	CV2260998	single nucleotide variant	NM_001282659.2(USP47):c.1859T>G (p.Met620Arg)	not specified [RCV004125875]	uncertain significance	11	11933925	11933925	Human		name
155969272	CV2262092	single nucleotide variant	NM_001282659.2(USP47):c.2164G>A (p.Val722Ile)	not specified [RCV004126558]	uncertain significance	11	11938343	11938343	Human		name
156258816	CV2277776	single nucleotide variant	NM_001282659.2(USP47):c.1189A>C (p.Met397Leu)	not specified [RCV004147208]	uncertain significance	11	11920465	11920465	Human		name
156046983	CV2315651	single nucleotide variant	NM_001282659.2(USP47):c.1850C>T (p.Ala617Val)	not specified [RCV004169683]	uncertain significance	11	11933916	11933916	Human		name
156175626	CV2355705	single nucleotide variant	NM_001282659.2(USP47):c.2023C>A (p.Leu675Met)	not specified [RCV004199067]	uncertain significance	11	11936456	11936456	Human		name
156335684	CV2363153	single nucleotide variant	NM_001282659.2(USP47):c.1565G>A (p.Ser522Asn)	not specified [RCV004211275]	uncertain significance	11	11930090	11930090	Human		name
155928695	CV2369545	single nucleotide variant	NM_001282659.2(USP47):c.2392C>T (p.His798Tyr)	not specified [RCV004214966]	uncertain significance	11	11942413	11942413	Human		name
155939896	CV2378889	single nucleotide variant	NM_001282659.2(USP47):c.2501A>G (p.Asp834Gly)	not specified [RCV004231323]	uncertain significance	11	11942522	11942522	Human		name
156156492	CV2393492	single nucleotide variant	NM_001282659.2(USP47):c.2199C>G (p.Ile733Met)	not specified [RCV004228981]	uncertain significance	11	11940434	11940434	Human		name
156224539	CV2395192	single nucleotide variant	NM_001282659.2(USP47):c.2657A>G (p.Glu886Gly)	not specified [RCV004236860]	uncertain significance	11	11942678	11942678	Human		name
329375372	CV2439947	single nucleotide variant	NM_001282659.2(USP47):c.1442G>C (p.Gly481Ala)	not specified [RCV004260428]	uncertain significance	11	11929489	11929489	Human		name
329352926	CV2468028	single nucleotide variant	NM_001282659.2(USP47):c.2332G>A (p.Glu778Lys)	not specified [RCV004273647]	uncertain significance	11	11942353	11942353	Human		name
401733288	CV2713038	single nucleotide variant	NM_001282659.2(USP47):c.1751G>A (p.Arg584His)	not specified [RCV004316598]	uncertain significance	11	11933103	11933103	Human		name
401856215	CV2761314	single nucleotide variant	NM_001282659.2(USP47):c.2482G>A (p.Asp828Asn)	not specified [RCV004341181]	uncertain significance	11	11942503	11942503	Human		name
401899942	CV2765752	single nucleotide variant	NM_001282659.2(USP47):c.2432A>G (p.Gln811Arg)	not specified [RCV004335755]	uncertain significance	11	11942453	11942453	Human		name
405800910	CV3338343	single nucleotide variant	NM_001282659.2(USP47):c.1787C>G (p.Pro596Arg)	not specified [RCV004477542]	uncertain significance	11	11933853	11933853	Human		name
405800911	CV3338344	single nucleotide variant	NM_001282659.2(USP47):c.2134A>G (p.Ile712Val)	not specified [RCV004477543]	likely benign	11	11938313	11938313	Human		name
405800913	CV3338345	single nucleotide variant	NM_001282659.2(USP47):c.2168C>A (p.Thr723Lys)	not specified [RCV004477544]	uncertain significance	11	11938347	11938347	Human		name
405800919	CV3338348	single nucleotide variant	NM_001282659.2(USP47):c.2937T>A (p.Asn979Lys)	not specified [RCV004477547]	uncertain significance	11	11942958	11942958	Human		name
405800986	CV3338359	single nucleotide variant	NM_001282659.2(USP47):c.1139T>C (p.Met380Thr)	not specified [RCV004477558]	uncertain significance	11	11920415	11920415	Human		name
405800988	CV3338360	single nucleotide variant	NM_001282659.2(USP47):c.1186G>C (p.Asp396His)	not specified [RCV004477559]	uncertain significance	11	11920462	11920462	Human		name
407528952	CV3487683	single nucleotide variant	NM_001282659.2(USP47):c.1960G>A (p.Gly654Arg)	not specified [RCV004680648]	uncertain significance	11	11936393	11936393	Human		name
407528954	CV3487684	single nucleotide variant	NM_001282659.2(USP47):c.2864A>T (p.Asp955Val)	not specified [RCV004680649]	uncertain significance	11	11942885	11942885	Human		name
597799065	CV3623180	single nucleotide variant	NM_001282659.2(USP47):c.2255G>A (p.Arg752His)	not specified [RCV004879515]	uncertain significance	11	11940490	11940490	Human		name
597696774	CV3623181	single nucleotide variant	NM_001282659.2(USP47):c.2036C>T (p.Thr679Met)	not specified [RCV004885194]	uncertain significance	11	11936469	11936469	Human		name
597799069	CV3623183	single nucleotide variant	NM_001282659.2(USP47):c.2237G>A (p.Arg746His)	not specified [RCV004879517]	uncertain significance	11	11940472	11940472	Human		name
597696787	CV3623184	single nucleotide variant	NM_001282659.2(USP47):c.2369A>G (p.His790Arg)	not specified [RCV004885195]	uncertain significance	11	11942390	11942390	Human		name
597696797	CV3623185	single nucleotide variant	NM_001282659.2(USP47):c.2219T>C (p.Met740Thr)	not specified [RCV004885196]	uncertain significance	11	11940454	11940454	Human		name
597799071	CV3623188	single nucleotide variant	NM_001282659.2(USP47):c.1243A>G (p.Thr415Ala)	not specified [RCV004879518]	uncertain significance	11	11922748	11922748	Human		name
597799076	CV3623190	single nucleotide variant	NM_001282659.2(USP47):c.2404A>G (p.Ile802Val)	not specified [RCV004879520]	uncertain significance	11	11942425	11942425	Human		name
597799080	CV3623192	single nucleotide variant	NM_001282659.2(USP47):c.2263A>G (p.Ser755Gly)	not specified [RCV004879522]	uncertain significance	11	11940498	11940498	Human		name
598238832	CV3932923	single nucleotide variant	NM_001282659.2(USP47):c.1060C>T (p.Arg354Trp)	not specified [RCV005296482]	uncertain significance	11	11920246	11920246	Human		name
598238844	CV3932927	single nucleotide variant	NM_001282659.2(USP47):c.1346A>T (p.Asn449Ile)	not specified [RCV005296484]	uncertain significance	11	11922851	11922851	Human		name
598204527	CV3932928	single nucleotide variant	NM_001282659.2(USP47):c.2003A>G (p.Lys668Arg)	not specified [RCV005290706]	uncertain significance	11	11936436	11936436	Human		name
598204532	CV3932929	single nucleotide variant	NM_001282659.2(USP47):c.2504A>G (p.Asp835Gly)	not specified [RCV005290707]	uncertain significance	11	11942525	11942525	Human		name
598238850	CV3932930	single nucleotide variant	NM_001282659.2(USP47):c.2383C>A (p.Leu795Met)	not specified [RCV005296485]	uncertain significance	11	11942404	11942404	Human		name
156236900	CV2206738	single nucleotide variant	NM_001282659.2(USP47):c.3878C>T (p.Ala1293Val)	not specified [RCV004083428]	uncertain significance	11	11955149	11955149	Human		name
156241428	CV2213929	single nucleotide variant	NM_001282659.2(USP47):c.3983A>G (p.His1328Arg)	not specified [RCV004083655]	uncertain significance	11	11956090	11956090	Human		name
156381614	CV2215088	single nucleotide variant	NM_001282659.2(USP47):c.3302G>A (p.Gly1101Glu)	not specified [RCV004084855]	uncertain significance	11	11948512	11948512	Human		name
155988914	CV2234260	single nucleotide variant	NM_001282659.2(USP47):c.3056A>T (p.Tyr1019Phe)	not specified [RCV004106333]	uncertain significance	11	11943077	11943077	Human		name
155976774	CV2246071	single nucleotide variant	NM_001282659.2(USP47):c.3800A>C (p.Asp1267Ala)	not specified [RCV004113980]	uncertain significance	11	11955071	11955071	Human		name
155984781	CV2270621	single nucleotide variant	NM_001282659.2(USP47):c.3338A>G (p.Asn1113Ser)	not specified [RCV004137837]	uncertain significance	11	11948548	11948548	Human		name
155923161	CV2347455	single nucleotide variant	NM_001282659.2(USP47):c.3692G>A (p.Ser1231Asn)	not specified [RCV004200407]	uncertain significance	11	11952849	11952849	Human		name
155904325	CV2385475	single nucleotide variant	NM_001282659.2(USP47):c.3632G>A (p.Arg1211Gln)	not specified [RCV004233122]	uncertain significance	11	11952789	11952789	Human		name
155962458	CV2388242	single nucleotide variant	NM_001282659.2(USP47):c.3986G>T (p.Arg1329Leu)	not specified [RCV004234700]	uncertain significance	11	11956093	11956093	Human		name
401753123	CV2674786	single nucleotide variant	NM_001282659.2(USP47):c.3332T>C (p.Leu1111Ser)	not specified [RCV004294065]	uncertain significance	11	11948542	11948542	Human		name
401889517	CV2756649	single nucleotide variant	NM_001282659.2(USP47):c.3418A>T (p.Ile1140Phe)	not specified [RCV004345166]	uncertain significance	11	11949958	11949958	Human		name
401870696	CV2766274	single nucleotide variant	NM_001282659.2(USP47):c.4027T>C (p.Tyr1343His)	not specified [RCV004342530]	uncertain significance	11	11956134	11956134	Human		name
405800921	CV3338349	single nucleotide variant	NM_001282659.2(USP47):c.3226C>T (p.Arg1076Trp)	not specified [RCV004477548]	uncertain significance	11	11948079	11948079	Human		name
405800923	CV3338350	single nucleotide variant	NM_001282659.2(USP47):c.3359T>G (p.Phe1120Cys)	not specified [RCV004477549]	uncertain significance	11	11949899	11949899	Human		name
405800925	CV3338351	single nucleotide variant	NM_001282659.2(USP47):c.3397C>T (p.Arg1133Trp)	not specified [RCV004477550]	uncertain significance	11	11949937	11949937	Human		name
405800927	CV3338352	single nucleotide variant	NM_001282659.2(USP47):c.3409G>A (p.Glu1137Lys)	not specified [RCV004477551]	uncertain significance	11	11949949	11949949	Human		name
405800928	CV3338353	single nucleotide variant	NM_001282659.2(USP47):c.3443G>A (p.Gly1148Asp)	not specified [RCV004477552]	uncertain significance	11	11949983	11949983	Human		name
405800930	CV3338354	single nucleotide variant	NM_001282659.2(USP47):c.3455G>C (p.Ser1152Thr)	not specified [RCV004477553]	uncertain significance	11	11949995	11949995	Human		name
405800932	CV3338355	single nucleotide variant	NM_001282659.2(USP47):c.3512T>C (p.Leu1171Ser)	not specified [RCV004477554]	uncertain significance	11	11950411	11950411	Human		name
405800980	CV3338356	single nucleotide variant	NM_001282659.2(USP47):c.3673G>A (p.Val1225Ile)	not specified [RCV004477555]	uncertain significance	11	11952830	11952830	Human		name
405800982	CV3338357	single nucleotide variant	NM_001282659.2(USP47):c.3884T>C (p.Ile1295Thr)	not specified [RCV004477556]	uncertain significance	11	11955155	11955155	Human		name
407528956	CV3487685	single nucleotide variant	NM_001282659.2(USP47):c.3071G>A (p.Gly1024Asp)	not specified [RCV004680650]	uncertain significance	11	11943092	11943092	Human		name
407528959	CV3487686	single nucleotide variant	NM_001282659.2(USP47):c.3394G>A (p.Val1132Ile)	not specified [RCV004680651]	uncertain significance	11	11949934	11949934	Human		name
597799067	CV3623182	single nucleotide variant	NM_001282659.2(USP47):c.3591G>C (p.Glu1197Asp)	not specified [RCV004879516]	uncertain significance	11	11952748	11952748	Human		name
597696806	CV3623187	single nucleotide variant	NM_001282659.2(USP47):c.3895G>C (p.Asp1299His)	not specified [RCV004885197]	uncertain significance	11	11956002	11956002	Human		name
597799074	CV3623189	single nucleotide variant	NM_001282659.2(USP47):c.3398G>A (p.Arg1133Gln)	not specified [RCV004879519]	uncertain significance	11	11949938	11949938	Human		name
597799078	CV3623191	single nucleotide variant	NM_001282659.2(USP47):c.3326A>T (p.Gln1109Leu)	not specified [RCV004879521]	uncertain significance	11	11948536	11948536	Human		name
597696816	CV3623193	single nucleotide variant	NM_001282659.2(USP47):c.3371C>T (p.Ala1124Val)	not specified [RCV004885198]	uncertain significance	11	11949911	11949911	Human		name
598204510	CV3932922	single nucleotide variant	NM_001282659.2(USP47):c.3707G>A (p.Arg1236Gln)	not specified [RCV005290703]	uncertain significance	11	11952864	11952864	Human		name
598238837	CV3932924	single nucleotide variant	NM_001282659.2(USP47):c.3883A>G (p.Ile1295Val)	not specified [RCV005296483]	uncertain significance	11	11955154	11955154	Human		name
598204516	CV3932925	single nucleotide variant	NM_001282659.2(USP47):c.3577C>A (p.Leu1193Ile)	not specified [RCV005290704]	uncertain significance	11	11950476	11950476	Human		name

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