Tead2 Variant Search Result - Rat Genome Database

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37 records found for search term Tead2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156087894	CV2290628	single nucleotide variant	NM_001256660.2(TEAD2):c.26C>T (p.Ala9Val)	not specified [RCV004149164]	uncertain significance	19	49360050	49360050	Human		name
401727558	CV2678376	single nucleotide variant	NM_001256660.2(TEAD2):c.13C>T (p.Arg5Trp)	not specified [RCV004292405]	uncertain significance	19	49360063	49360063	Human		name
329386455	CV2456020	single nucleotide variant	NM_001256660.2(TEAD2):c.50C>T (p.Thr17Met)	not specified [RCV004272925]	uncertain significance	19	49360026	49360026	Human		name
597773729	CV3612711	single nucleotide variant	NM_001256660.2(TEAD2):c.41G>A (p.Ser14Asn)	not specified [RCV004872128]	uncertain significance	19	49360035	49360035	Human		name
156330373	CV2210608	single nucleotide variant	NM_001256660.2(TEAD2):c.109G>A (p.Gly37Arg)	not specified [RCV004083758]	uncertain significance	19	49359967	49359967	Human		name
156365421	CV2272109	single nucleotide variant	NM_001256660.2(TEAD2):c.137G>A (p.Ser46Asn)	not specified [RCV004124894]	uncertain significance	19	49359939	49359939	Human		name
407517858	CV3486079	single nucleotide variant	NM_001256660.2(TEAD2):c.225G>C (p.Lys75Asn)	not specified [RCV004675760]	uncertain significance	19	49359851	49359851	Human		name
155922896	CV2217507	single nucleotide variant	NM_001256660.2(TEAD2):c.646A>C (p.Thr216Pro)	not specified [RCV004090049]	uncertain significance	19	49348804	49348804	Human		name
156199399	CV2237545	single nucleotide variant	NM_001256660.2(TEAD2):c.728C>T (p.Pro243Leu)	not specified [RCV004106486]	uncertain significance	19	49348722	49348722	Human		name
155915836	CV2274416	single nucleotide variant	NM_001256660.2(TEAD2):c.584C>T (p.Pro195Leu)	not specified [RCV004136786]	uncertain significance	19	49351321	49351321	Human		name
156009070	CV2294300	single nucleotide variant	NM_001256660.2(TEAD2):c.610G>A (p.Glu204Lys)	not specified [RCV004151429]	uncertain significance	19	49348840	49348840	Human		name
156325114	CV2335164	single nucleotide variant	NM_001256660.2(TEAD2):c.653C>T (p.Ser218Leu)	not specified [RCV004184694]	uncertain significance	19	49348797	49348797	Human		name
156135656	CV2379940	single nucleotide variant	NM_001256660.2(TEAD2):c.946G>A (p.Gly316Ser)	not specified [RCV004222086]	uncertain significance	19	49343374	49343374	Human		name
329397320	CV2460145	single nucleotide variant	NM_001256660.2(TEAD2):c.433A>G (p.Ile145Val)	not specified [RCV004273250]	uncertain significance	19	49355359	49355359	Human		name
405765536	CV3328322	single nucleotide variant	NM_001256660.2(TEAD2):c.326G>C (p.Arg109Pro)	not specified [RCV004469376]	uncertain significance	19	49357286	49357286	Human		name
405765542	CV3328323	single nucleotide variant	NM_001256660.2(TEAD2):c.542T>C (p.Val181Ala)	not specified [RCV004469377]	uncertain significance	19	49351363	49351363	Human		name
405765549	CV3328324	single nucleotide variant	NM_001256660.2(TEAD2):c.674G>A (p.Arg225Gln)	not specified [RCV004469378]	uncertain significance	19	49348776	49348776	Human		name
405765557	CV3328325	single nucleotide variant	NM_001256660.2(TEAD2):c.884G>A (p.Arg295His)	not specified [RCV004469379]	uncertain significance	19	49347227	49347227	Human		name
407517855	CV3486078	single nucleotide variant	NM_001256660.2(TEAD2):c.745T>A (p.Ser249Thr)	not specified [RCV004675759]	uncertain significance	19	49348705	49348705	Human		name
597773719	CV3612709	single nucleotide variant	NM_001256660.2(TEAD2):c.673C>T (p.Arg225Trp)	not specified [RCV004872126]	uncertain significance	19	49348777	49348777	Human		name
597773725	CV3612710	single nucleotide variant	NM_001256660.2(TEAD2):c.629C>T (p.Ser210Leu)	not specified [RCV004872127]	uncertain significance	19	49348821	49348821	Human		name
598164074	CV3923894	single nucleotide variant	NM_001256660.2(TEAD2):c.504G>T (p.Trp168Cys)	not specified [RCV005283229]	uncertain significance	19	49355183	49355183	Human		name
598164086	CV3923897	single nucleotide variant	NM_001256660.2(TEAD2):c.923C>T (p.Ala308Val)	not specified [RCV005283231]	uncertain significance	19	49343397	49343397	Human		name
598210796	CV3923898	single nucleotide variant	NM_001256660.2(TEAD2):c.826C>T (p.Arg276Trp)	not specified [RCV005291903]	uncertain significance	19	49347285	49347285	Human		name
598210803	CV3923899	single nucleotide variant	NM_001256660.2(TEAD2):c.572T>C (p.Leu191Ser)	not specified [RCV005291904]	uncertain significance	19	49351333	49351333	Human		name
598210820	CV3923901	single nucleotide variant	NM_001256660.2(TEAD2):c.703G>C (p.Val235Leu)	not specified [RCV005291906]	uncertain significance	19	49348747	49348747	Human		name
598164092	CV3923902	single nucleotide variant	NM_001256660.2(TEAD2):c.670G>A (p.Ala224Thr)	not specified [RCV005283232]	uncertain significance	19	49348780	49348780	Human		name
598210827	CV3923903	single nucleotide variant	NM_001256660.2(TEAD2):c.404C>T (p.Thr135Ile)	not specified [RCV005291907]	uncertain significance	19	49355388	49355388	Human		name
15176560	CV705154	single nucleotide variant	NM_001256660.2(TEAD2):c.677G>C (p.Gly226Ala)	not provided [RCV000950852]	benign	19	49348773	49348773	Human		name
15171521	CV705155	single nucleotide variant	NM_001256660.2(TEAD2):c.348G>T (p.Gln116His)	not provided [RCV000949848]	benign	19	49357264	49357264	Human		name
15148383	CV716595	single nucleotide variant	NM_001256660.2(TEAD2):c.637C>T (p.Pro213Ser)	not provided [RCV000967534]	benign	19	49348813	49348813	Human		name
401898282	CV2791169	single nucleotide variant	NM_001256660.2(TEAD2):c.1216G>A (p.Val406Ile)	not specified [RCV004356525]	uncertain significance	19	49342464	49342464	Human		name
405765530	CV3328321	single nucleotide variant	NM_001256660.2(TEAD2):c.1174C>A (p.His392Asn)	not specified [RCV004469375]	uncertain significance	19	49342506	49342506	Human		name
407519698	CV3486077	single nucleotide variant	NM_001256660.2(TEAD2):c.1153G>A (p.Glu385Lys)	not specified [RCV004676648]	uncertain significance	19	49342527	49342527	Human		name
597773731	CV3612712	single nucleotide variant	NM_001256660.2(TEAD2):c.1339C>T (p.Arg447Cys)	not specified [RCV004872129]	uncertain significance	19	49341341	49341341	Human		name
597773737	CV3612713	single nucleotide variant	NM_001256660.2(TEAD2):c.1316G>A (p.Arg439His)	not specified [RCV004872130]	uncertain significance	19	49341364	49341364	Human		name
598210810	CV3923900	single nucleotide variant	NM_001256660.2(TEAD2):c.1304C>T (p.Ser435Phe)	not specified [RCV005291905]	uncertain significance	19	49341376	49341376	Human		name

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