Daxx Variant Search Result - Rat Genome Database

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63 records found for search term Daxx

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156053039	CV2388503	single nucleotide variant	NM_001141969.2(DAXX):c.-84G>A	not specified [RCV004237356]	likely benign	6	33322893	33322893	Human		name
401866423	CV2775545	single nucleotide variant	NM_001141969.2(DAXX):c.-63C>T	not specified [RCV004350716]	uncertain significance	6	33322872	33322872	Human		name
8632020	CV87226	single nucleotide variant	NM_001141969.1(DAXX):c.210C>T (p.Phe70=)	Malignant melanoma [RCV000067317]	not provided	6	33321565	33321565	Human		name
155921910	CV2350742	single nucleotide variant	NM_001141969.2(DAXX):c.77A>C (p.His26Pro)	not specified [RCV004207083]	uncertain significance	6	33321849	33321849	Human		name
156073072	CV2240631	single nucleotide variant	NM_001141969.2(DAXX):c.238G>C (p.Asp80His)	not specified [RCV004119271]	uncertain significance	6	33321537	33321537	Human		name
156072296	CV2289922	single nucleotide variant	NM_001141969.2(DAXX):c.130C>A (p.Pro44Thr)	not specified [RCV004150574]	uncertain significance	6	33321796	33321796	Human		name
401760656	CV2706038	single nucleotide variant	NM_001141969.2(DAXX):c.236C>T (p.Ala79Val)	not specified [RCV004314738]	uncertain significance	6	33321539	33321539	Human		name
401877900	CV2757680	single nucleotide variant	NM_001141969.2(DAXX):c.290C>T (p.Ser97Phe)	not specified [RCV004334789]	uncertain significance	6	33321485	33321485	Human		name
598251787	CV3963439	single nucleotide variant	NM_001141969.2(DAXX):c.276G>C (p.Gln92His)	not specified [RCV005323129]	uncertain significance	6	33321499	33321499	Human		name
15169131	CV721990	single nucleotide variant	NM_001141969.2(DAXX):c.1317C>T (p.Asp439=)	not provided [RCV000883204]	benign	6	33320159	33320159	Human		name
156136917	CV2210332	single nucleotide variant	NM_001141969.2(DAXX):c.344G>A (p.Arg115Gln)	not specified [RCV004089488]	uncertain significance	6	33321431	33321431	Human		name
156336890	CV2228606	single nucleotide variant	NM_001141969.2(DAXX):c.766C>T (p.Arg256Cys)	not specified [RCV004092834]	uncertain significance	6	33321009	33321009	Human		name
155946939	CV2262499	single nucleotide variant	NM_001141969.2(DAXX):c.640G>C (p.Glu214Gln)	not specified [RCV004128929]	uncertain significance	6	33321135	33321135	Human		name
156396425	CV2326267	single nucleotide variant	NM_001141969.2(DAXX):c.488A>C (p.His163Pro)	not specified [RCV004180519]	uncertain significance	6	33321287	33321287	Human		name
156044997	CV2397179	single nucleotide variant	NM_001141969.2(DAXX):c.308C>T (p.Ala103Val)	not specified [RCV004238719]	uncertain significance	6	33321467	33321467	Human		name
401724924	CV2715028	single nucleotide variant	NM_001141969.2(DAXX):c.860G>A (p.Gly287Glu)	not specified [RCV004322340]	uncertain significance	6	33320915	33320915	Human		name
401883481	CV2754329	single nucleotide variant	NM_001141969.2(DAXX):c.350G>A (p.Arg117Gln)	not specified [RCV004334505]	likely benign	6	33321425	33321425	Human		name
405689023	CV3246387	single nucleotide variant	NM_001141969.2(DAXX):c.485C>T (p.Thr162Ile)	not specified [RCV004372957]	uncertain significance	6	33321290	33321290	Human		name
405689029	CV3246388	single nucleotide variant	NM_001141969.2(DAXX):c.607C>T (p.Arg203Trp)	not specified [RCV004372958]	uncertain significance	6	33321168	33321168	Human		name
405689035	CV3246389	single nucleotide variant	NM_001141969.2(DAXX):c.827A>G (p.Asn276Ser)	not specified [RCV004372959]	uncertain significance	6	33320948	33320948	Human		name
407453057	CV3430143	single nucleotide variant	NM_001141969.2(DAXX):c.608G>A (p.Arg203Gln)	not specified [RCV004608811]	uncertain significance	6	33321167	33321167	Human		name
407453063	CV3430146	single nucleotide variant	NM_001141969.2(DAXX):c.305C>T (p.Ser102Leu)	not specified [RCV004608814]	uncertain significance	6	33321470	33321470	Human		name
597800460	CV3651770	single nucleotide variant	NM_001141969.2(DAXX):c.916C>G (p.Arg306Gly)	not specified [RCV004905695]	uncertain significance	6	33320859	33320859	Human		name
597800454	CV3655277	single nucleotide variant	NM_001141969.2(DAXX):c.736T>C (p.Ser246Pro)	not specified [RCV004905692]	uncertain significance	6	33321039	33321039	Human		name
598251758	CV3963434	single nucleotide variant	NM_001141969.2(DAXX):c.647A>G (p.Asp216Gly)	not specified [RCV005323124]	uncertain significance	6	33321128	33321128	Human		name
598251771	CV3963436	single nucleotide variant	NM_001141969.2(DAXX):c.383A>G (p.Asn128Ser)	not specified [RCV005323126]	uncertain significance	6	33321392	33321392	Human		name
13463001	CV439678	deletion	NM_001141969.2(DAXX):c.1178del (p.Lys393fs)	Metastatic pancreatic neuroendocrine tumours [RCV000515528]	likely pathogenic	6	33320453	33320453	Human		name
13462997	CV439684	single nucleotide variant	NM_001141969.2(DAXX):c.850C>T (p.Pro284Ser)	Metastatic pancreatic neuroendocrine tumours [RCV000515521]	likely pathogenic	6	33320925	33320925	Human		name
156123134	CV2233945	single nucleotide variant	NM_001141969.2(DAXX):c.1198G>C (p.Gly400Arg)	not specified [RCV004104291]	uncertain significance	6	33320433	33320433	Human		name
329391400	CV2448518	single nucleotide variant	NM_001141969.2(DAXX):c.1066G>A (p.Val356Met)	not specified [RCV004259203]	uncertain significance	6	33320565	33320565	Human		name
401721130	CV2673611	single nucleotide variant	NM_001141969.2(DAXX):c.1901A>C (p.Lys634Thr)	not specified [RCV004282346]	uncertain significance	6	33319419	33319419	Human		name
401767169	CV2681497	single nucleotide variant	NM_001141969.2(DAXX):c.1817G>T (p.Gly606Val)	not specified [RCV004292031]	uncertain significance	6	33319503	33319503	Human		name
401743467	CV2715488	single nucleotide variant	NM_001141969.2(DAXX):c.1042G>A (p.Val348Ile)	not specified [RCV004326585]	likely benign	6	33320589	33320589	Human		name
401737730	CV2718192	single nucleotide variant	NM_001141969.2(DAXX):c.2114G>A (p.Arg705Gln)	not specified [RCV004315888]	likely benign	6	33319046	33319046	Human		name
405688979	CV3246378	single nucleotide variant	NM_001141969.2(DAXX):c.1247G>A (p.Gly416Asp)	not specified [RCV004372948]	uncertain significance	6	33320384	33320384	Human		name
405688991	CV3246380	single nucleotide variant	NM_001141969.2(DAXX):c.1318G>A (p.Asp440Asn)	not specified [RCV004372950]	uncertain significance	6	33320158	33320158	Human		name
405688996	CV3246381	single nucleotide variant	NM_001141969.2(DAXX):c.1417G>A (p.Gly473Ser)	not specified [RCV004372951]	uncertain significance	6	33320059	33320059	Human		name
405689000	CV3246382	single nucleotide variant	NM_001141969.2(DAXX):c.1511A>G (p.Asn504Ser)	not specified [RCV004372952]	uncertain significance	6	33319809	33319809	Human		name
405689005	CV3246383	single nucleotide variant	NM_001141969.2(DAXX):c.1610C>T (p.Pro537Leu)	not specified [RCV004372953]	uncertain significance	6	33319710	33319710	Human		name
405689010	CV3246384	single nucleotide variant	NM_001141969.2(DAXX):c.1958G>A (p.Arg653Lys)	not specified [RCV004372954]	likely benign	6	33319202	33319202	Human		name
405689013	CV3246385	single nucleotide variant	NM_001141969.2(DAXX):c.2014C>T (p.Pro672Ser)	not specified [RCV004372955]	likely benign	6	33319146	33319146	Human		name
405689018	CV3246386	single nucleotide variant	NM_001141969.2(DAXX):c.2113C>T (p.Arg705Trp)	not specified [RCV004372956]	likely benign	6	33319047	33319047	Human		name
407453055	CV3430142	single nucleotide variant	NM_001141969.2(DAXX):c.1490T>C (p.Met497Thr)	not specified [RCV004608810]	likely benign	6	33319830	33319830	Human		name
407453061	CV3430145	single nucleotide variant	NM_001141969.2(DAXX):c.1187C>T (p.Ala396Val)	not specified [RCV004608813]	uncertain significance	6	33320444	33320444	Human		name
407453065	CV3430147	single nucleotide variant	NM_001141969.2(DAXX):c.1918G>A (p.Gly640Arg)	not specified [RCV004608815]	uncertain significance	6	33319402	33319402	Human		name
407453067	CV3430148	single nucleotide variant	NM_001141969.2(DAXX):c.2105C>T (p.Ser702Phe)	not specified [RCV004608816]	likely benign	6	33319055	33319055	Human		name
597800462	CV3651771	single nucleotide variant	NM_001141969.2(DAXX):c.1244C>T (p.Ser415Phe)	not specified [RCV004905696]	uncertain significance	6	33320387	33320387	Human		name
597800448	CV3655274	single nucleotide variant	NM_001141969.2(DAXX):c.1805A>C (p.Glu602Ala)	not specified [RCV004905689]	uncertain significance	6	33319515	33319515	Human		name
597800450	CV3655275	single nucleotide variant	NM_001141969.2(DAXX):c.1708G>C (p.Glu570Gln)	not specified [RCV004905690]	uncertain significance	6	33319612	33319612	Human		name
597800452	CV3655276	single nucleotide variant	NM_001141969.2(DAXX):c.1335G>C (p.Glu445Asp)	not specified [RCV004905691]	likely benign	6	33320141	33320141	Human		name
597800456	CV3655278	single nucleotide variant	NM_001141969.2(DAXX):c.1240G>A (p.Asp414Asn)	not specified [RCV004905693]	uncertain significance	6	33320391	33320391	Human		name
597800458	CV3655279	single nucleotide variant	NM_001141969.2(DAXX):c.1581A>G (p.Ile527Met)	not specified [RCV004905694]	likely benign	6	33319739	33319739	Human		name
598251752	CV3963433	single nucleotide variant	NM_001141969.2(DAXX):c.2092C>T (p.Leu698Phe)	not specified [RCV005323123]	uncertain significance	6	33319068	33319068	Human		name
598251765	CV3963435	single nucleotide variant	NM_001141969.2(DAXX):c.1111C>T (p.Arg371Trp)	not specified [RCV005323125]	uncertain significance	6	33320520	33320520	Human		name
598251777	CV3963437	single nucleotide variant	NM_001141969.2(DAXX):c.2120C>T (p.Ser707Phe)	not specified [RCV005323127]	uncertain significance	6	33319040	33319040	Human		name
598251782	CV3963438	single nucleotide variant	NM_001141969.2(DAXX):c.1670T>C (p.Leu557Pro)	not specified [RCV005323128]	likely benign	6	33319650	33319650	Human		name
598251798	CV3963441	single nucleotide variant	NM_001141969.2(DAXX):c.2146C>T (p.Arg716Trp)	not specified [RCV005323131]	uncertain significance	6	33319014	33319014	Human		name
598251803	CV3963442	single nucleotide variant	NM_001141969.2(DAXX):c.1318G>T (p.Asp440Tyr)	not specified [RCV005323132]	uncertain significance	6	33320158	33320158	Human		name
598251809	CV3963443	single nucleotide variant	NM_001141969.2(DAXX):c.1990T>C (p.Cys664Arg)	not specified [RCV005323133]	likely benign	6	33319170	33319170	Human		name
15137971	CV710450	single nucleotide variant	NM_001141969.2(DAXX):c.1123G>A (p.Val375Ile)	not provided [RCV000965709]	benign	6	33320508	33320508	Human		name
15191260	CV721989	single nucleotide variant	NM_001141969.2(DAXX):c.1457C>G (p.Ala486Gly)	not provided [RCV000888329]	benign	6	33320019	33320019	Human		name
13462996	CV439686	deletion	NM_001141969.2(DAXX):c.801_824del (p.Arg269_Asn276del)	Metastatic pancreatic neuroendocrine tumours [RCV000515520]	likely pathogenic	6	33320951	33320974	Human		name
13462998	CV439680	microsatellite	NM_001141969.2(DAXX):c.329_330del (p.Leu109_Ser110insTer)	Metastatic pancreatic neuroendocrine tumours [RCV000515523]	likely pathogenic	6	33321445	33321446	Human		name

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