Rnf20 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

191 records found for search term Rnf20

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15170297	CV759847	single nucleotide variant	NM_019592.7(RNF20):c.2752-9T>C	not provided [RCV000927671]	likely benign	9	101562237	101562237	Human		name
156368600	CV2193730	single nucleotide variant	NM_019592.7(RNF20):c.38C>T (p.Pro13Leu)	not specified [RCV004074493]	uncertain significance	9	101535461	101535461	Human		name
156001250	CV2378792	single nucleotide variant	NM_019592.7(RNF20):c.41G>C (p.Gly14Ala)	not specified [RCV004231241]	uncertain significance	9	101535464	101535464	Human		name
8689440	CV139350	single nucleotide variant	NM_019592.7(RNF20):c.247C>T (p.Gln83Ter)	not provided [RCV000122608]	not provided	9	101540320	101540320	Human		name
155927742	CV2285239	single nucleotide variant	NM_019592.7(RNF20):c.152T>G (p.Leu51Arg)	not specified [RCV004145437]	uncertain significance	9	101540225	101540225	Human		name
401911053	CV2826246	single nucleotide variant	NM_019592.7(RNF20):c.1695T>C (p.Asp565=)	not provided [RCV003425726]	likely benign	9	101552547	101552547	Human		name
405697995	CV3313209	single nucleotide variant	NM_019592.7(RNF20):c.222G>C (p.Glu74Asp)	not specified [RCV004446585]	uncertain significance	9	101540295	101540295	Human		name
597687364	CV3590340	single nucleotide variant	NM_019592.7(RNF20):c.245G>A (p.Arg82Gln)	not specified [RCV004858485]	uncertain significance	9	101540318	101540318	Human		name
598204685	CV3909567	single nucleotide variant	NM_019592.7(RNF20):c.226A>G (p.Ile76Val)	not specified [RCV005269586]	uncertain significance	9	101540299	101540299	Human		name
15115991	CV711674	single nucleotide variant	NM_019592.7(RNF20):c.1881A>G (p.Lys627=)	not provided [RCV000961956]	benign	9	101552733	101552733	Human		name
156242016	CV2261983	single nucleotide variant	NM_019592.7(RNF20):c.601C>T (p.Leu201Phe)	not specified [RCV004126474]	uncertain significance	9	101540948	101540948	Human		name
156204108	CV2331607	single nucleotide variant	NM_019592.7(RNF20):c.544C>T (p.Arg182Cys)	not specified [RCV004184243]	uncertain significance	9	101540891	101540891	Human		name
156193092	CV2350475	single nucleotide variant	NM_019592.7(RNF20):c.310A>G (p.Ile104Val)	not specified [RCV004204842]	uncertain significance	9	101540502	101540502	Human		name
156057912	CV2396404	single nucleotide variant	NM_019592.7(RNF20):c.706A>C (p.Thr236Pro)	not specified [RCV004242123]	uncertain significance	9	101544844	101544844	Human		name
329400606	CV2438553	single nucleotide variant	NM_019592.7(RNF20):c.548G>A (p.Arg183Gln)	not specified [RCV004261735]	uncertain significance	9	101540895	101540895	Human		name
401767938	CV2678112	single nucleotide variant	NM_019592.7(RNF20):c.752C>G (p.Ser251Cys)	not specified [RCV004296626]	uncertain significance	9	101546824	101546824	Human		name
405698001	CV3313210	single nucleotide variant	NM_019592.7(RNF20):c.305A>G (p.Glu102Gly)	not specified [RCV004446586]	uncertain significance	9	101540497	101540497	Human		name
405698007	CV3313211	single nucleotide variant	NM_019592.7(RNF20):c.647A>C (p.Glu216Ala)	not specified [RCV004446587]	uncertain significance	9	101544785	101544785	Human		name
405698012	CV3313212	single nucleotide variant	NM_019592.7(RNF20):c.730C>T (p.Arg244Cys)	not specified [RCV004446588]	uncertain significance	9	101544868	101544868	Human		name
405698018	CV3313213	single nucleotide variant	NM_019592.7(RNF20):c.806C>T (p.Ser269Phe)	not specified [RCV004446589]	uncertain significance	9	101546878	101546878	Human		name
405698022	CV3313214	single nucleotide variant	NM_019592.7(RNF20):c.883G>T (p.Val295Phe)	not specified [RCV004446590]	uncertain significance	9	101546955	101546955	Human		name
597687377	CV3590342	single nucleotide variant	NM_019592.7(RNF20):c.379C>T (p.Leu127Phe)	not specified [RCV004858486]	uncertain significance	9	101540571	101540571	Human		name
597687395	CV3590345	single nucleotide variant	NM_019592.7(RNF20):c.621C>G (p.Asn207Lys)	not specified [RCV004858488]	uncertain significance	9	101540968	101540968	Human		name
597755088	CV3590351	single nucleotide variant	NM_019592.7(RNF20):c.371G>A (p.Arg124Gln)	not specified [RCV004847531]	uncertain significance	9	101540563	101540563	Human		name
598204681	CV3909566	single nucleotide variant	NM_019592.7(RNF20):c.632A>C (p.Asn211Thr)	not specified [RCV005269585]	uncertain significance	9	101544770	101544770	Human		name
598204704	CV3909570	single nucleotide variant	NM_019592.7(RNF20):c.587A>G (p.Gln196Arg)	not specified [RCV005269589]	uncertain significance	9	101540934	101540934	Human		name
15130145	CV751290	single nucleotide variant	NM_019592.7(RNF20):c.676G>A (p.Ala226Thr)	not provided [RCV000919955]	likely benign	9	101544814	101544814	Human		name
8633155	CV88368	single nucleotide variant	NM_019592.6(RNF20):c.718C>T (p.Gln240Ter)	Malignant melanoma [RCV000068460]	not provided	9	101544856	101544856	Human		name
156070694	CV2204061	single nucleotide variant	NM_019592.7(RNF20):c.2447T>C (p.Ile816Thr)	not specified [RCV004076528]	uncertain significance	9	101560865	101560865	Human		name
156145820	CV2218839	single nucleotide variant	NM_019592.7(RNF20):c.1856G>A (p.Arg619Gln)	not specified [RCV004085080]	uncertain significance	9	101552708	101552708	Human		name
155939551	CV2225565	single nucleotide variant	NM_019592.7(RNF20):c.2642G>A (p.Arg881Gln)	not specified [RCV004100944]	uncertain significance	9	101561223	101561223	Human		name
156298107	CV2247001	single nucleotide variant	NM_019592.7(RNF20):c.1586C>T (p.Pro529Leu)	not specified [RCV004114567]	uncertain significance	9	101552438	101552438	Human		name
156113612	CV2261459	single nucleotide variant	NM_019592.7(RNF20):c.1331C>T (p.Thr444Ile)	not specified [RCV004130082]	uncertain significance	9	101551742	101551742	Human		name
156264563	CV2289895	single nucleotide variant	NM_019592.7(RNF20):c.2900A>C (p.Asn967Thr)	not specified [RCV004150553]	uncertain significance	9	101562394	101562394	Human		name
156120037	CV2354135	single nucleotide variant	NM_019592.7(RNF20):c.1694A>G (p.Asp565Gly)	not specified [RCV004206572]	uncertain significance	9	101552546	101552546	Human		name
155928459	CV2360035	single nucleotide variant	NM_019592.7(RNF20):c.1691G>C (p.Arg564Pro)	not specified [RCV004212870]	uncertain significance	9	101552543	101552543	Human		name
156261586	CV2381393	single nucleotide variant	NM_019592.7(RNF20):c.1049G>A (p.Arg350Gln)	not specified [RCV004227442]	uncertain significance	9	101547475	101547475	Human		name
155999453	CV2396423	single nucleotide variant	NM_019592.7(RNF20):c.1111G>T (p.Val371Leu)	not specified [RCV004242139]	uncertain significance	9	101550624	101550624	Human		name
329356452	CV2430757	single nucleotide variant	NM_019592.7(RNF20):c.1528A>G (p.Lys510Glu)	not specified [RCV004253938]	uncertain significance	9	101552260	101552260	Human		name
329354468	CV2448231	single nucleotide variant	NM_019592.7(RNF20):c.1123G>A (p.Val375Ile)	not specified [RCV004263437]	uncertain significance	9	101550636	101550636	Human		name
329397608	CV2466140	single nucleotide variant	NM_019592.7(RNF20):c.2417A>G (p.Glu806Gly)	not specified [RCV004279793]	uncertain significance	9	101560835	101560835	Human		name
329380354	CV2466578	single nucleotide variant	NM_019592.7(RNF20):c.1009G>C (p.Glu337Gln)	not specified [RCV004274110]	uncertain significance	9	101547435	101547435	Human		name
329388298	CV2468866	single nucleotide variant	NM_019592.7(RNF20):c.1604A>G (p.Glu535Gly)	not specified [RCV004280169]	uncertain significance	9	101552456	101552456	Human		name
401761494	CV2702362	single nucleotide variant	NM_019592.7(RNF20):c.1601C>T (p.Ala534Val)	not specified [RCV004316889]	uncertain significance	9	101552453	101552453	Human		name
401746063	CV2734351	single nucleotide variant	NM_019592.7(RNF20):c.1690C>G (p.Arg564Gly)	not specified [RCV004332533]	uncertain significance	9	101552542	101552542	Human		name
401861174	CV2769553	single nucleotide variant	NM_019592.7(RNF20):c.2068A>G (p.Lys690Glu)	not specified [RCV004351205]	uncertain significance	9	101554742	101554742	Human		name
401862198	CV2775192	single nucleotide variant	NM_019592.7(RNF20):c.1304G>C (p.Arg435Thr)	not specified [RCV004346537]	uncertain significance	9	101551715	101551715	Human		name
401874715	CV2781180	single nucleotide variant	NM_019592.7(RNF20):c.1096G>A (p.Glu366Lys)	not specified [RCV004352228]	uncertain significance	9	101550609	101550609	Human		name
405697977	CV3313206	single nucleotide variant	NM_019592.7(RNF20):c.1577C>T (p.Thr526Ile)	not specified [RCV004446582]	uncertain significance	9	101552429	101552429	Human		name
405697983	CV3313207	single nucleotide variant	NM_019592.7(RNF20):c.2044A>C (p.Lys682Gln)	not specified [RCV004446583]	uncertain significance	9	101554718	101554718	Human		name
405697988	CV3313208	single nucleotide variant	NM_019592.7(RNF20):c.2066A>C (p.Lys689Thr)	not specified [RCV004446584]	uncertain significance	9	101554740	101554740	Human		name
407486437	CV3479678	single nucleotide variant	NM_019592.7(RNF20):c.1601C>G (p.Ala534Gly)	not specified [RCV004665461]	uncertain significance	9	101552453	101552453	Human		name
407508727	CV3479679	single nucleotide variant	NM_019592.7(RNF20):c.2612C>T (p.Thr871Ile)	not specified [RCV004672137]	uncertain significance	9	101561193	101561193	Human		name
407486443	CV3479680	single nucleotide variant	NM_019592.7(RNF20):c.2555A>T (p.Glu852Val)	not specified [RCV004665462]	uncertain significance	9	101561136	101561136	Human		name
407486450	CV3479681	single nucleotide variant	NM_019592.7(RNF20):c.2462A>G (p.Lys821Arg)	not specified [RCV004665463]	uncertain significance	9	101560880	101560880	Human		name
597755070	CV3590341	single nucleotide variant	NM_019592.7(RNF20):c.2701A>G (p.Asn901Asp)	not specified [RCV004847526]	uncertain significance	9	101561961	101561961	Human		name
597687404	CV3590346	single nucleotide variant	NM_019592.7(RNF20):c.1577C>A (p.Thr526Asn)	not specified [RCV004858489]	uncertain significance	9	101552429	101552429	Human		name
597755077	CV3590347	single nucleotide variant	NM_019592.7(RNF20):c.1552G>T (p.Ala518Ser)	not specified [RCV004847528]	uncertain significance	9	101552404	101552404	Human		name
597687410	CV3590348	single nucleotide variant	NM_019592.7(RNF20):c.1229A>G (p.His410Arg)	not specified [RCV004858490]	uncertain significance	9	101550742	101550742	Human		name
597755082	CV3590349	single nucleotide variant	NM_019592.7(RNF20):c.2684C>A (p.Thr895Asn)	not specified [RCV004847529]	uncertain significance	9	101561944	101561944	Human		name
597755085	CV3590350	single nucleotide variant	NM_019592.7(RNF20):c.2414T>A (p.Leu805Gln)	not specified [RCV004847530]	uncertain significance	9	101560832	101560832	Human		name
598204692	CV3909568	single nucleotide variant	NM_019592.7(RNF20):c.1855C>T (p.Arg619Trp)	not specified [RCV005269587]	uncertain significance	9	101552707	101552707	Human		name
598204697	CV3909569	single nucleotide variant	NM_019592.7(RNF20):c.1600G>A (p.Ala534Thr)	not specified [RCV005269588]	uncertain significance	9	101552452	101552452	Human		name
15195922	CV723230	single nucleotide variant	NM_019592.7(RNF20):c.2539C>T (p.Leu847Phe)	not provided [RCV000889637]	likely benign	9	101561120	101561120	Human		name
8626625	CV81769	single nucleotide variant	NM_019592.6(RNF20):c.2770T>G (p.Cys924Gly)	Malignant melanoma [RCV000061847]	not provided	9	101562264	101562264	Human		name
21072320	CV792718	single nucleotide variant	NM_207396.3(RNF207):c.1109+1G>A	Long QT syndrome [RCV000991411]	likely pathogenic	1	6211119	6211119	Human	2	name
156383137	CV2361425	single nucleotide variant	NM_031297.7(RNF208):c.4C>T (p.Pro2Ser)	not specified [RCV004221070]	uncertain significance	9	137221209	137221209	Human		name
401882308	CV2781650	single nucleotide variant	NM_207396.3(RNF207):c.5C>G (p.Ser2Trp)	not specified [RCV004354852]	uncertain significance	1	6206540	6206540	Human		name
405698236	CV3313230	single nucleotide variant	NM_031297.7(RNF208):c.17G>T (p.Gly6Val)	not specified [RCV004446606]	uncertain significance	9	137221196	137221196	Human		name
155922858	CV2347396	single nucleotide variant	NM_031297.7(RNF208):c.94G>A (p.Ala32Thr)	not specified [RCV004207236]	uncertain significance	9	137221119	137221119	Human		name
405698225	CV3313228	single nucleotide variant	NM_207396.3(RNF207):c.74G>A (p.Cys25Tyr)	not specified [RCV004446604]	uncertain significance	1	6206609	6206609	Human		name
597687509	CV3590369	single nucleotide variant	NM_031297.7(RNF208):c.49C>T (p.Leu17Phe)	not specified [RCV004858501]	uncertain significance	9	137221164	137221164	Human		name
15162768	CV732536	single nucleotide variant	NM_207396.3(RNF207):c.519G>A (p.Leu173=)	not provided [RCV000903627]	likely benign	1	6209164	6209164	Human		name
156125885	CV2223617	single nucleotide variant	NM_207396.3(RNF207):c.101G>A (p.Arg34His)	not specified [RCV004093754]	uncertain significance	1	6206636	6206636	Human		name
155978159	CV2247002	single nucleotide variant	NM_207396.3(RNF207):c.221G>A (p.Gly74Glu)	not specified [RCV004114568]	uncertain significance	1	6207408	6207408	Human		name
156152431	CV2307630	single nucleotide variant	NM_031297.7(RNF208):c.287G>A (p.Arg96Gln)	not specified [RCV004168048]	uncertain significance	9	137220926	137220926	Human		name
156051657	CV2324133	single nucleotide variant	NM_031297.7(RNF208):c.281T>A (p.Leu94Gln)	not specified [RCV004178416]	uncertain significance	9	137220932	137220932	Human		name
156157668	CV2363731	single nucleotide variant	NM_207396.3(RNF207):c.179G>A (p.Cys60Tyr)	not specified [RCV004218719]	uncertain significance	1	6206714	6206714	Human		name
156270423	CV2398676	single nucleotide variant	NM_207396.3(RNF207):c.230C>T (p.Pro77Leu)	not specified [RCV004240024]	uncertain significance	1	6207417	6207417	Human		name
329372286	CV2443092	single nucleotide variant	NM_207396.3(RNF207):c.136G>A (p.Ala46Thr)	not specified [RCV004253678]	uncertain significance	1	6206671	6206671	Human		name
329391017	CV2447625	single nucleotide variant	NM_207396.3(RNF207):c.277G>A (p.Val93Met)	not specified [RCV004258428]	uncertain significance	1	6207464	6207464	Human		name
401758292	CV2678327	single nucleotide variant	NM_207396.3(RNF207):c.220G>A (p.Gly74Arg)	not specified [RCV004290316]	uncertain significance	1	6207407	6207407	Human		name
401878851	CV2770373	single nucleotide variant	NM_207396.3(RNF207):c.257T>C (p.Val86Ala)	not specified [RCV004358022]	uncertain significance	1	6207444	6207444	Human		name
405698034	CV3313216	single nucleotide variant	NM_207396.3(RNF207):c.117C>G (p.Asp39Glu)	not specified [RCV004446592]	uncertain significance	1	6206652	6206652	Human		name
405698179	CV3313219	single nucleotide variant	NM_207396.3(RNF207):c.134G>A (p.Cys45Tyr)	not specified [RCV004446595]	uncertain significance	1	6206669	6206669	Human		name
405698204	CV3313224	single nucleotide variant	NM_207396.3(RNF207):c.290G>C (p.Arg97Pro)	not specified [RCV004446600]	uncertain significance	1	6207477	6207477	Human		name
405698240	CV3313231	single nucleotide variant	NM_031297.7(RNF208):c.283C>A (p.Pro95Thr)	not specified [RCV004446607]	uncertain significance	9	137220930	137220930	Human		name
407508741	CV3479690	single nucleotide variant	NM_207396.3(RNF207):c.160A>G (p.Thr54Ala)	not specified [RCV004672141]	uncertain significance	1	6206695	6206695	Human		name
407486487	CV3479692	single nucleotide variant	NM_031297.7(RNF208):c.295C>T (p.Arg99Cys)	not specified [RCV004665469]	uncertain significance	9	137220918	137220918	Human		name
597687439	CV3590356	single nucleotide variant	NM_207396.3(RNF207):c.200C>T (p.Thr67Met)	not specified [RCV004858493]	uncertain significance	1	6207387	6207387	Human		name
597755107	CV3590359	single nucleotide variant	NM_207396.3(RNF207):c.163G>A (p.Asp55Asn)	not specified [RCV004847536]	uncertain significance	1	6206698	6206698	Human		name
597755116	CV3590367	single nucleotide variant	NM_031297.7(RNF208):c.160C>T (p.Pro54Ser)	not specified [RCV004847538]	uncertain significance	9	137221053	137221053	Human		name
598204716	CV3909572	single nucleotide variant	NM_207396.3(RNF207):c.104C>T (p.Pro35Leu)	not specified [RCV005269591]	uncertain significance	1	6206639	6206639	Human		name
598204770	CV3909580	single nucleotide variant	NM_207396.3(RNF207):c.277G>T (p.Val93Leu)	not specified [RCV005269599]	uncertain significance	1	6207464	6207464	Human		name
598204802	CV3909585	single nucleotide variant	NM_207396.3(RNF207):c.233T>C (p.Val78Ala)	not specified [RCV005269604]	uncertain significance	1	6207420	6207420	Human		name
156126575	CV2234400	single nucleotide variant	NM_207396.3(RNF207):c.811G>A (p.Glu271Lys)	not specified [RCV004100619]	uncertain significance	1	6210233	6210233	Human		name
156050712	CV2237833	single nucleotide variant	NM_031297.7(RNF208):c.389C>T (p.Ser130Leu)	not specified [RCV004109072]	uncertain significance	9	137220824	137220824	Human		name
156243760	CV2242981	single nucleotide variant	NM_031297.7(RNF208):c.569G>T (p.Arg190Leu)	not specified [RCV004107861]	uncertain significance	9	137220644	137220644	Human		name
156184878	CV2251620	single nucleotide variant	NM_207396.3(RNF207):c.356G>A (p.Cys119Tyr)	not specified [RCV004117853]	uncertain significance	1	6208912	6208912	Human		name
156147099	CV2289327	single nucleotide variant	NM_207396.3(RNF207):c.834G>T (p.Glu278Asp)	not specified [RCV004152301]	uncertain significance	1	6210256	6210256	Human		name
156085691	CV2295272	single nucleotide variant	NM_207396.3(RNF207):c.969C>G (p.Ile323Met)	not specified [RCV004158645]	uncertain significance	1	6210896	6210896	Human		name
155972619	CV2335818	single nucleotide variant	NM_031297.7(RNF208):c.401C>T (p.Ser134Leu)	not specified [RCV004196053]	uncertain significance	9	137220812	137220812	Human		name
155969121	CV2339386	single nucleotide variant	NM_031297.7(RNF208):c.759C>A (p.Asn253Lys)	not specified [RCV004191609]	uncertain significance	9	137220454	137220454	Human		name
156196156	CV2347667	single nucleotide variant	NM_207396.3(RNF207):c.844C>T (p.His282Tyr)	not specified [RCV004200600]	uncertain significance	1	6210266	6210266	Human		name
156387664	CV2372816	single nucleotide variant	NM_031297.7(RNF208):c.682G>A (p.Gly228Arg)	not specified [RCV004221999]	uncertain significance	9	137220531	137220531	Human		name
156146775	CV2381809	single nucleotide variant	NM_031297.7(RNF208):c.769G>A (p.Ala257Thr)	not specified [RCV004232255]	uncertain significance	9	137220444	137220444	Human		name
329372289	CV2443093	single nucleotide variant	NM_207396.3(RNF207):c.664A>G (p.Ile222Val)	not specified [RCV004253679]	uncertain significance	1	6209450	6209450	Human		name
401768385	CV2716509	single nucleotide variant	NM_031297.7(RNF208):c.571C>G (p.Arg191Gly)	not specified [RCV004327596]	uncertain significance	9	137220642	137220642	Human		name
401764639	CV2721430	single nucleotide variant	NM_207396.3(RNF207):c.986A>C (p.His329Pro)	not specified [RCV004322169]	uncertain significance	1	6210913	6210913	Human		name
405698210	CV3313225	single nucleotide variant	NM_207396.3(RNF207):c.515T>G (p.Leu172Trp)	not specified [RCV004446601]	uncertain significance	1	6209160	6209160	Human		name
405698216	CV3313226	single nucleotide variant	NM_207396.3(RNF207):c.571G>A (p.Val191Met)	not specified [RCV004446602]	uncertain significance	1	6209287	6209287	Human		name
405698221	CV3313227	single nucleotide variant	NM_207396.3(RNF207):c.673C>G (p.Leu225Val)	not specified [RCV004446603]	uncertain significance	1	6209459	6209459	Human		name
405698230	CV3313229	single nucleotide variant	NM_207396.3(RNF207):c.785T>C (p.Leu262Pro)	not specified [RCV004446605]	uncertain significance	1	6209955	6209955	Human		name
405698244	CV3313232	single nucleotide variant	NM_031297.7(RNF208):c.326G>A (p.Arg109His)	not specified [RCV004446608]	uncertain significance	9	137220887	137220887	Human		name
405698249	CV3313233	single nucleotide variant	NM_031297.7(RNF208):c.404C>T (p.Ala135Val)	not specified [RCV004446609]	uncertain significance	9	137220809	137220809	Human		name
405698263	CV3313235	single nucleotide variant	NM_031297.7(RNF208):c.599G>A (p.Gly200Asp)	not specified [RCV004446611]	uncertain significance	9	137220614	137220614	Human		name
407486477	CV3479686	single nucleotide variant	NM_207396.3(RNF207):c.742G>C (p.Gly248Arg)	not specified [RCV004665467]	uncertain significance	1	6209528	6209528	Human		name
407508744	CV3479691	single nucleotide variant	NM_031297.7(RNF208):c.370C>T (p.Arg124Trp)	not specified [RCV004672142]	uncertain significance	9	137220843	137220843	Human		name
407486492	CV3479693	single nucleotide variant	NM_031297.7(RNF208):c.331G>T (p.Ala111Ser)	not specified [RCV004665470]	uncertain significance	9	137220882	137220882	Human		name
407486500	CV3479694	single nucleotide variant	NM_031297.7(RNF208):c.412G>A (p.Gly138Ser)	not specified [RCV004665471]	uncertain significance	9	137220801	137220801	Human		name
597755099	CV3590357	single nucleotide variant	NM_207396.3(RNF207):c.404G>T (p.Arg135Leu)	not specified [RCV004847534]	uncertain significance	1	6208960	6208960	Human		name
597755111	CV3590363	single nucleotide variant	NM_207396.3(RNF207):c.376C>T (p.Arg126Cys)	not specified [RCV004847537]	uncertain significance	1	6208932	6208932	Human		name
597687480	CV3590365	single nucleotide variant	NM_207396.3(RNF207):c.380G>A (p.Cys127Tyr)	not specified [RCV004858498]	uncertain significance	1	6208936	6208936	Human		name
597687500	CV3590368	single nucleotide variant	NM_031297.7(RNF208):c.754C>T (p.Arg252Trp)	not specified [RCV004858500]	uncertain significance	9	137220459	137220459	Human		name
597755119	CV3590370	single nucleotide variant	NM_031297.7(RNF208):c.718C>G (p.Arg240Gly)	not specified [RCV004847539]	uncertain significance	9	137220495	137220495	Human		name
597755123	CV3590371	single nucleotide variant	NM_031297.7(RNF208):c.452A>C (p.Asn151Thr)	not specified [RCV004847540]	uncertain significance	9	137220761	137220761	Human		name
597755128	CV3590372	single nucleotide variant	NM_031297.7(RNF208):c.314T>C (p.Leu105Pro)	not specified [RCV004847541]	uncertain significance	9	137220899	137220899	Human		name
598204732	CV3909574	single nucleotide variant	NM_207396.3(RNF207):c.437G>A (p.Gly146Asp)	not specified [RCV005269593]	uncertain significance	1	6208993	6208993	Human		name
598204765	CV3909579	single nucleotide variant	NM_207396.3(RNF207):c.299A>G (p.Asn100Ser)	not specified [RCV005269598]	uncertain significance	1	6207486	6207486	Human		name
598204776	CV3909581	single nucleotide variant	NM_207396.3(RNF207):c.977G>T (p.Arg326Leu)	not specified [RCV005269600]	uncertain significance	1	6210904	6210904	Human		name
598204790	CV3909583	single nucleotide variant	NM_207396.3(RNF207):c.949A>C (p.Met317Leu)	not specified [RCV005269602]	uncertain significance	1	6210876	6210876	Human		name
598204814	CV3909587	single nucleotide variant	NM_207396.3(RNF207):c.322C>G (p.Gln108Glu)	not specified [RCV005269606]	uncertain significance	1	6207509	6207509	Human		name
598204822	CV3909588	single nucleotide variant	NM_031297.7(RNF208):c.328G>A (p.Val110Met)	not specified [RCV005269607]	uncertain significance	9	137220885	137220885	Human		name
598204828	CV3909589	single nucleotide variant	NM_031297.7(RNF208):c.568C>T (p.Arg190Cys)	not specified [RCV005269608]	uncertain significance	9	137220645	137220645	Human		name
598204835	CV3909590	single nucleotide variant	NM_031297.7(RNF208):c.755G>A (p.Arg252Gln)	not specified [RCV005269609]	uncertain significance	9	137220458	137220458	Human		name
598204842	CV3909591	single nucleotide variant	NM_031297.7(RNF208):c.563C>T (p.Thr188Ile)	not specified [RCV005269610]	uncertain significance	9	137220650	137220650	Human		name
598204851	CV3909592	single nucleotide variant	NM_031297.7(RNF208):c.695A>G (p.Glu232Gly)	not specified [RCV005269611]	uncertain significance	9	137220518	137220518	Human		name
150476256	CV1263618	single nucleotide variant	NM_207396.3(RNF207):c.1718A>G (p.Asn573Ser)	not provided [RCV001685141]	benign	1	6218354	6218354	Human	4	name
156158846	CV2236147	single nucleotide variant	NM_207396.3(RNF207):c.1439C>T (p.Ser480Leu)	not specified [RCV004114291]	uncertain significance	1	6212373	6212373	Human		name
156359626	CV2257837	single nucleotide variant	NM_207396.3(RNF207):c.1606C>T (p.Pro536Ser)	not specified [RCV004127886]	uncertain significance	1	6213137	6213137	Human		name
156157185	CV2262382	single nucleotide variant	NM_207396.3(RNF207):c.1006A>G (p.Ser336Gly)	not specified [RCV004128831]	uncertain significance	1	6210933	6210933	Human		name
156254857	CV2280926	single nucleotide variant	NM_207396.3(RNF207):c.1488G>T (p.Trp496Cys)	not specified [RCV004145169]	uncertain significance	1	6212687	6212687	Human		name
156271276	CV2290301	single nucleotide variant	NM_207396.3(RNF207):c.1496C>T (p.Ala499Val)	not specified [RCV004154736]	uncertain significance	1	6212695	6212695	Human		name
156007845	CV2299780	single nucleotide variant	NM_207396.3(RNF207):c.1873G>A (p.Asp625Asn)	not specified [RCV004148938]	uncertain significance	1	6219375	6219375	Human		name
156058222	CV2305227	single nucleotide variant	NM_207396.3(RNF207):c.1269C>G (p.His423Gln)	not specified [RCV004171157]	uncertain significance	1	6212026	6212026	Human		name
156060540	CV2305414	single nucleotide variant	NM_207396.3(RNF207):c.1426G>T (p.Val476Leu)	not specified [RCV004165140]	uncertain significance	1	6212360	6212360	Human		name
156278425	CV2325048	single nucleotide variant	NM_207396.3(RNF207):c.1070G>A (p.Gly357Glu)	not specified [RCV004175590]	uncertain significance	1	6211079	6211079	Human		name
156360929	CV2329707	single nucleotide variant	NM_207396.3(RNF207):c.1246G>C (p.Glu416Gln)	not specified [RCV004180812]	uncertain significance	1	6212003	6212003	Human		name
156080898	CV2337607	single nucleotide variant	NM_207396.3(RNF207):c.1370C>T (p.Ser457Leu)	not specified [RCV004181171]	uncertain significance	1	6212304	6212304	Human		name
156045468	CV2340180	single nucleotide variant	NM_207396.3(RNF207):c.1435G>A (p.Ala479Thr)	not specified [RCV004192414]	uncertain significance	1	6212369	6212369	Human		name
155910795	CV2366658	single nucleotide variant	NM_207396.3(RNF207):c.1075C>T (p.Arg359Cys)	not specified [RCV004210665]	uncertain significance	1	6211084	6211084	Human		name
156263463	CV2374392	single nucleotide variant	NM_207396.3(RNF207):c.1130C>T (p.Pro377Leu)	not specified [RCV004231912]	uncertain significance	1	6211887	6211887	Human		name
156090249	CV2375183	single nucleotide variant	NM_207396.3(RNF207):c.1426G>A (p.Val476Met)	not specified [RCV004230223]	uncertain significance	1	6212360	6212360	Human		name
156070978	CV2381354	single nucleotide variant	NM_207396.3(RNF207):c.1705G>A (p.Asp569Asn)	not specified [RCV004227409]	uncertain significance	1	6218341	6218341	Human		name
329361281	CV2436856	single nucleotide variant	NM_207396.3(RNF207):c.1202C>T (p.Thr401Met)	not specified [RCV004260247]	uncertain significance	1	6211959	6211959	Human		name
329365792	CV2441052	single nucleotide variant	NM_207396.3(RNF207):c.1136C>T (p.Ala379Val)	not specified [RCV004261420]	likely benign	1	6211893	6211893	Human		name
329392896	CV2469049	single nucleotide variant	NM_207396.3(RNF207):c.1589T>C (p.Ile530Thr)	not specified [RCV004274293]	uncertain significance	1	6213120	6213120	Human		name
401731606	CV2674430	single nucleotide variant	NM_207396.3(RNF207):c.1393G>A (p.Gly465Arg)	not specified [RCV004289294]	uncertain significance	1	6212327	6212327	Human		name
401757763	CV2707956	single nucleotide variant	NM_207396.3(RNF207):c.1745G>C (p.Gly582Ala)	not specified [RCV004309220]	uncertain significance	1	6219247	6219247	Human		name
401896952	CV2785438	single nucleotide variant	NM_207396.3(RNF207):c.1711A>G (p.Arg571Gly)	not specified [RCV004362979]	uncertain significance	1	6218347	6218347	Human		name
401864637	CV2791203	single nucleotide variant	NM_207396.3(RNF207):c.1210C>T (p.Arg404Trp)	not specified [RCV004356847]	uncertain significance	1	6211967	6211967	Human		name
401860782	CV2794514	single nucleotide variant	NM_207396.3(RNF207):c.1744G>A (p.Gly582Arg)	not provided [RCV003387682]	uncertain significance	1	6219246	6219246	Human		name
405698026	CV3313215	single nucleotide variant	NM_207396.3(RNF207):c.1076G>A (p.Arg359His)	not specified [RCV004446591]	uncertain significance	1	6211085	6211085	Human		name
405698041	CV3313217	single nucleotide variant	NM_207396.3(RNF207):c.1205T>G (p.Leu402Arg)	not specified [RCV004446593]	uncertain significance	1	6211962	6211962	Human		name
405698045	CV3313218	single nucleotide variant	NM_207396.3(RNF207):c.1294C>T (p.Arg432Trp)	not specified [RCV004446594]	uncertain significance	1	6212051	6212051	Human		name
405698184	CV3313220	single nucleotide variant	NM_207396.3(RNF207):c.1522G>C (p.Glu508Gln)	not specified [RCV004446596]	uncertain significance	1	6212721	6212721	Human		name
405698190	CV3313221	single nucleotide variant	NM_207396.3(RNF207):c.1558C>A (p.Leu520Met)	not specified [RCV004446597]	uncertain significance	1	6213089	6213089	Human		name
405698196	CV3313222	single nucleotide variant	NM_207396.3(RNF207):c.1604C>T (p.Thr535Met)	not specified [RCV004446598]	uncertain significance	1	6213135	6213135	Human		name
407508731	CV3479682	single nucleotide variant	NM_207396.3(RNF207):c.1264G>A (p.Glu422Lys)	not specified [RCV004672138]	uncertain significance	1	6212021	6212021	Human		name
407486456	CV3479683	single nucleotide variant	NM_207396.3(RNF207):c.1189G>A (p.Val397Ile)	not specified [RCV004665464]	uncertain significance	1	6211946	6211946	Human		name
407486470	CV3479685	single nucleotide variant	NM_207396.3(RNF207):c.1505G>A (p.Arg502Gln)	not specified [RCV004665466]	likely benign	1	6212704	6212704	Human		name
407508734	CV3479687	single nucleotide variant	NM_207396.3(RNF207):c.1028G>A (p.Arg343Gln)	not specified [RCV004672139]	uncertain significance	1	6211037	6211037	Human		name
407508737	CV3479688	single nucleotide variant	NM_207396.3(RNF207):c.1871G>A (p.Gly624Asp)	not specified [RCV004672140]	uncertain significance	1	6219373	6219373	Human		name
407486482	CV3479689	single nucleotide variant	NM_207396.3(RNF207):c.1079G>A (p.Arg360Gln)	not specified [RCV004665468]	uncertain significance	1	6211088	6211088	Human		name
597755092	CV3590352	single nucleotide variant	NM_207396.3(RNF207):c.1274G>A (p.Arg425His)	not specified [RCV004847532]	uncertain significance	1	6212031	6212031	Human		name
597755095	CV3590353	single nucleotide variant	NM_207396.3(RNF207):c.1849A>G (p.Arg617Gly)	not specified [RCV004847533]	uncertain significance	1	6219351	6219351	Human		name
597687419	CV3590354	single nucleotide variant	NM_207396.3(RNF207):c.1039G>A (p.Ala347Thr)	not specified [RCV004858491]	uncertain significance	1	6211048	6211048	Human		name
597755104	CV3590358	single nucleotide variant	NM_207396.3(RNF207):c.1447G>A (p.Ala483Thr)	not specified [RCV004847535]	likely benign	1	6212381	6212381	Human		name
597687447	CV3590360	single nucleotide variant	NM_207396.3(RNF207):c.1802C>T (p.Pro601Leu)	not specified [RCV004858494]	likely benign	1	6219304	6219304	Human		name
597687455	CV3590361	single nucleotide variant	NM_207396.3(RNF207):c.1838T>C (p.Met613Thr)	not specified [RCV004858495]	uncertain significance	1	6219340	6219340	Human		name
597687463	CV3590362	single nucleotide variant	NM_207396.3(RNF207):c.1386G>T (p.Glu462Asp)	not specified [RCV004858496]	uncertain significance	1	6212320	6212320	Human		name
597687472	CV3590364	single nucleotide variant	NM_207396.3(RNF207):c.1576T>C (p.Tyr526His)	not specified [RCV004858497]	uncertain significance	1	6213107	6213107	Human		name
597687490	CV3590366	single nucleotide variant	NM_207396.3(RNF207):c.1799C>T (p.Ala600Val)	not specified [RCV004858499]	uncertain significance	1	6219301	6219301	Human		name
598204710	CV3909571	single nucleotide variant	NM_207396.3(RNF207):c.1387A>T (p.Ile463Phe)	not specified [RCV005269590]	uncertain significance	1	6212321	6212321	Human		name
598204740	CV3909575	single nucleotide variant	NM_207396.3(RNF207):c.1253C>T (p.Thr418Met)	not specified [RCV005269594]	uncertain significance	1	6212010	6212010	Human		name
598204746	CV3909576	single nucleotide variant	NM_207396.3(RNF207):c.1724C>T (p.Ala575Val)	not specified [RCV005269595]	uncertain significance	1	6218360	6218360	Human		name
598204752	CV3909577	single nucleotide variant	NM_207396.3(RNF207):c.1295G>T (p.Arg432Leu)	not specified [RCV005269596]	uncertain significance	1	6212052	6212052	Human		name
598204759	CV3909578	single nucleotide variant	NM_207396.3(RNF207):c.1255C>T (p.Pro419Ser)	not specified [RCV005269597]	uncertain significance	1	6212012	6212012	Human		name
598204797	CV3909584	single nucleotide variant	NM_207396.3(RNF207):c.1741C>G (p.Pro581Ala)	not specified [RCV005269603]	uncertain significance	1	6219243	6219243	Human		name
598204807	CV3909586	single nucleotide variant	NM_207396.3(RNF207):c.1033G>A (p.Glu345Lys)	not specified [RCV005269605]	uncertain significance	1	6211042	6211042	Human		name
329846371	CV2524694	deletion	NM_207396.3(RNF207):c.1889_1892del (p.Arg630fs)	not provided [RCV003228177]	uncertain significance	1	6219388	6219391	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