iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs3679788	snp	C/T	0.492188	0.0620098	intron-variant	Tdrd3	Mm_Celera	14:87521930	TTGAGTTATGACTTA[C/T]AAAGAGCTTATTATG	219249
rs3680448	snp	A/T	0.492188	0.0620098	intron-variant	Tdrd3	Mm_Celera	14:87522014	AAAAATTGTGATCAT[A/T]TAATCTTTTTAAATG	219249
rs3680634	snp	A/G	0.492188	0.0620098	intron-variant	Tdrd3	GRCm38.p3	14:87522094	TAAGCACTTATCTTA[A/G]AAGACTTAGGTTAAA	219249
rs3696103	snp	C/T	0.492188	0.0620098	intron-variant	Tdrd3	Mm_Celera	14:87522289	CTTACCTCCCTTCTC[C/T]GCCTCTCTTCTTCCT	219249
rs3707983	snp	A/C/T	0.473373	0.11227	intron-variant	Tdrd3	GRCm38.p3	14:87463728	AATTATAAGAGATAG[A/C/T]GTAGTTTGAATGCTT	219249
rs3709345	snp	A/C/G	0.5	0	intron-variant	Tdrd3	GRCm38.p3	14:87463970	CAGAACTATCTGAGC[A/C/G]AGTTGCCTATGGAGC	219249
rs4138641	snp	A/G	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87463522	tgtgtgtgtgtgtgt[A/G]tgtTATATCTCATGA	219249
rs6171492	snp	C/T	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87465738	TAACAGAAACTACCA[C/T]GGTGAGCTCAGCCTT	219249
rs6172038	snp	C/T	0.345679	0.230967	intron-variant	Tdrd3	Mm_Celera	14:87465854	CATTTCCAGTTAGGC[C/T]TCAAAGAATGATATT	219249
rs6172101	snp	C/T	0.345679	0.230967	intron-variant	Tdrd3	Mm_Celera	14:87465886	TCATTGCTCTGGATG[C/T]CACTTCTGCTTTCAG	219249
rs6172605	snp	A/G	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87465942	AGGTCAGCGTGCTTG[A/G]GGGAGGCAGCTCCAC	219249
rs6256136	snp	A/T	0.497778	0.0332592	intron-variant	Tdrd3	Mm_Celera	14:87522410	TTACAGCTTAGATTG[A/T]GCTTCTGCTGTCTGA	219249
rs6312952	snp	A/C	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87526002	TCGTTCATGAAGAAA[A/C]ATTTTCCTAACATGG	219249
rs6313026	snp	C/T	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87526063	ACATTCGTCATCATT[C/T]CTGTGTTATAATGAT	219249
rs6313059	snp	A/G	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87526087	TAATGATAACATATT[A/G]TCCATCTGTAGCCAT	219249
rs6325899	snp	A/G	0.444444	0.157135	intron-variant	Tdrd3	Mm_Celera	14:87526106	ATCTGTAGCCATAGA[A/G]TTTAAGAGTAGAATA	219249
rs6326580	snp	A/G	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87526275	AAGTGCTGCCATGCC[A/G]AGANACTGGCATGCT	219249
rs6326588	snp	G/T	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87526279	GCTGCCATGCCNAGA[G/T]ACTGGCATGCTTTCT	219249
rs6327046	snp	C/G	0.49827	0.0293608	intron-variant	Tdrd3	Mm_Celera	14:87526332	GCATCAGATCTCACC[C/G]TTCCTTATGCTGTGA	219249
rs6327158	snp	A/G	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87526391	AGGGAGGTGACCAAC[A/G]GGTGAGAAGCACTGG	219249
rs6327652	snp	G/T	0.497778	0.0332592	intron-variant	Tdrd3	GRCm38.p3	14:87526482	ATGTTTTAACACTCA[G/T]TAAAATAGCTACTAA	219249
rs13468107	snp	A/G			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	Tdrd3	Mm_Celera	14:87416798	CGTCCCCGAGCCTGA[A/G]CAGCTAACCATGGCC	219249
rs13482288	snp	A/G	0.499541	0.0151446	intron-variant	Tdrd3	Mm_Celera	14:87427815	GGACAGTTCTGCTTT[A/G]TGTTTTGGTCACCTT	219249
rs29125324	snp	A/G	0.492188	0.0620098	intron-variant	Tdrd3	GRCm38.p3	14:87467686	AGGAAACGCTAGGAC[A/G]CTTGTCTGCTTTCTC	219249
rs29135435	snp	C/T	0.415225	0.187619	intron-variant	Tdrd3	GRCm38.p3	14:87467896	CACCAAGACCATGAG[C/T]GTCTGAGCACACTGG	219249
rs29137449	snp	A/G	0.497778	0.0332592	intron-variant	Tdrd3	GRCm38.p3	14:87467910	AAGAGATGTGCAGCC[A/G]CCAAGACCATGAGTG	219249
rs29151390	snp	G/T	0.415225	0.187619	intron-variant	Tdrd3	GRCm38.p3	14:87467103	TCACAACTCATCCCA[G/T]AGTTTGAAAGCCAAC	219249
rs29151954	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Tdrd3	GRCm38.p3	14:87470576	TAAAGGTCAGTTACT[C/T]GATATGATCAAGAAA	219249
rs29157411	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Tdrd3	GRCm38.p3	14:87469776	TATGCACACATGTAT[A/G]TAAAATGCCAAAATT	219249
rs29164938	snp	A/G	0.408163	0.193609	intron-variant	Tdrd3	GRCm38.p3	14:87467067	AGAGAGAAAAGCTAC[A/G]ACTATGAATAGCCCT	219249
rs29167125	snp	A/G	0.5	0	intron-variant	Tdrd3	GRCm38.p3	14:87469087	CAACAAAGCAAGCCA[A/G]GCTCTCAAAGAAACA	219249
rs29167739	snp	C/T	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87472483	TAAACAGTGAATTTC[C/T]GGAAAAGATTTTCTG	219249
rs29170427	snp	C/G	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87467625	CCCCAAACTCAGAGA[C/G]TTTAGGTTCCAGTGC	219249
rs29173564	snp	A/G	0.429688	0.173817	intron-variant	Tdrd3	GRCm38.p3	14:87468050	CAGAGCAAGTTTGAT[A/G]CCATTAAGTGTTAGT	219249
rs29174378	snp	C/T	0.5	0	intron-variant	Tdrd3	GRCm38.p3	14:87467426	CACATATACTATATA[C/T]ACATGTGTAATATAC	219249
rs29174447	snp	C/T	0.484429	0.0868505	intron-variant	Tdrd3	GRCm38.p3	14:87472544	AAGTACAGCTGCTAA[C/T]CTGTTGGGGAAAAAA	219249
rs29176746	snp	C/T	0.5	0	intron-variant	Tdrd3	GRCm38.p3	14:87467995	ATGGAAAAGCTACCC[C/T]TAAAACTATTTGGCA	219249
rs29181122	snp	C/T	0.444444	0.157135	intron-variant	Tdrd3	GRCm38.p3	14:87466898	GTCCTAAGGCCCACA[C/T]GGTAAGAGGAAAGAA	219249
rs29189765	snp	C/T	0.5	0	intron-variant	Tdrd3	GRCm38.p3	14:87467331	TTTCCCAAGGATTTA[C/T]TTTTATTTATGTGTA	219249
rs29190304	snp	C/T	0.375	0.216506	intron-variant	Tdrd3	GRCm38.p3	14:87467435	AAATATATACACATA[C/T]ACTATATATACATGT	219249
rs29195979	snp	A/G	0.375	0.216506	intron-variant	Tdrd3	GRCm38.p3	14:87467412	ATACATGTGTAATAT[A/G]CATATATATTTTAAT	219249
rs29209418	snp	C/T	0.375	0.216506	intron-variant	Tdrd3	GRCm38.p3	14:87467452	TTTTATGTATATCTA[C/T]TAAATATATACACAT	219249
rs29212875	snp	C/T	0.345679	0.230967	intron-variant	Tdrd3	GRCm38.p3	14:87467819	TCACTGCTCTGAACA[C/T]AGCCTCGTTCTGCCG	219249
rs29214728	snp	C/T	0.444444	0.157135	intron-variant	Tdrd3	GRCm38.p3	14:87472011	TCAATGACACAATTT[C/T]CCTATCTTTAATTGT	219249
rs29216979	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Tdrd3	GRCm38.p3	14:87469623	GAAACAAGGAAACAC[A/G]AATGGCCAATAAGTA	219249
rs29223221	snp	A/G	0.465374	0.126941	intron-variant, utr-variant-5-prime	Tdrd3	GRCm38.p3	14:87471697	AAAGGAATGCTTCCT[A/G]TTCAAACAGCAACTT	219249
rs30112014	snp	A/T	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87491133	GCCTTTCCTTCTCAG[A/T]GCAGCAGGCAGATGA	219249
rs30114582	snp	A/T	0.49827	0.0293608	intron-variant	Tdrd3	Mm_Celera	14:87487444	AGGAGAAAGTTTTGA[A/T]GTTGCATTCTGAGAA	219249
rs30125356	snp	C/T	0.48	0.0979796	intron-variant	Tdrd3	Mm_Celera	14:87435996	ACCAGAAGTCCAGTC[C/T]AATAACAAACTCCAA	219249
rs30126297	snp	A/G	0.5	0	intron-variant, downstream-variant-500B	Tdrd3, Gm33076	Mm_Celera	14:87532718	GACCAGGCTGGCCTC[A/G]AACTCAGAAATTCGC	219249
rs30139609	snp	C/T	0.444444	0.157135	intron-variant	Tdrd3	Mm_Celera	14:87498797	GAGTCTTGCTGATGG[C/T]TTATGGAGGGCAACC	219249
rs30141580	snp	A/G	0.359862	0.224567	intron-variant	Tdrd3	Mm_Celera	14:87541355	CACACAGATCAAAGA[A/G]GAGTTGCTGCATAAC	219249
rs30142554	snp	A/G	0.432133	0.171253	intron-variant	Tdrd3	Mm_Celera	14:87425054	GCTGAGTTCAGTTTC[A/G]AGGACTTGTTATAAG	219249
rs30148376	snp	A/C	0.498615	0.0262793	intron-variant	Tdrd3	Mm_Celera	14:87486759	GACTGATATTCTAAA[A/C]TTTCTGTGACTGTGT	219249
rs30157636	snp	C/T	0.48	0.0979796	intron-variant	Tdrd3	Mm_Celera	14:87428974	AATAGTTATTGGTAA[C/T]ATTTTAAGCAAAAGT	219249
rs30164565	snp	G/T	0.444444	0.157135	missense, nc-transcript-variant	Tdrd3	Mm_Celera	14:87506292	ATGAATAGTGAAGCT[G/T]TTAGTGGTCTAAAAA	219249
rs30169419	snp	C/T	0.493827	0.0552116	intron-variant	Tdrd3	Mm_Celera	14:87539647	TGATGCAGCTTCCAG[C/T]TGACAGTATGATGTG	219249
rs30187699	snp	C/G	0.444444	0.157135	intron-variant	Tdrd3	Mm_Celera	14:87496210	AGGTCCATCCATTTG[C/G]CTAGGAATTTCATAA	219249
rs30194760	snp	C/T	0.42	0.183303	intron-variant	Tdrd3	Mm_Celera	14:87427664	AATATACAGACTGGA[C/T]TGAGTGAGGCACACA	219249
rs30204367	snp	G/T	0.5	0	utr-variant-3-prime, intron-variant	Tdrd3	Mm_Celera	14:87513121	TATATGGTGGTCTCA[G/T]AGAGCCCAGGCTGTA	219249
rs30204718	snp	C/T	0.497041	0.0383476	utr-variant-3-prime, intron-variant	Tdrd3	Mm_Celera	14:87512368	GTGTTTGATAGCACT[C/T]TCTTGACTTTCTATA	219249
rs30211295	snp	C/G	0.444444	0.157135	intron-variant	Tdrd3	Mm_Celera	14:87427218	AGGCTGGCCTCTAAC[C/G]CAGAGATCCGGACTG	219249
rs30213406	snp	C/T	0.375	0.216506	intron-variant	Tdrd3	Mm_Celera	14:87475228	AGACACACAGACAAG[C/T]GTGCATACACTCTTG	219249
rs30246836	snp	C/T	0.375	0.216506	intron-variant	Tdrd3	Mm_Celera	14:87483777	CACTTGTGTGGTAAA[C/T]ATTTGGAGTTTGTAA	219249
rs30250081	snp	C/T	0.444444	0.157135	intron-variant	Tdrd3	Mm_Celera	14:87462382	TTGGCAGGCCCCTGC[C/T]AAGTAAGGATCCCTT	219249
rs30253057	snp	A/T	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87529033	ATCTGATGCTGTCTG[A/T]CCTCCGTGGACACTG	219249
rs30253915	snp	A/C	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87435099	AGACTGCCTGAGGCT[A/C]AATTGAAGAGTTTTG	219249
rs30255494	snp	A/T	0.48	0.0979796	intron-variant	Tdrd3	Mm_Celera	14:87424864	TAAAACATTTAGTGA[A/T]TTTGGAAAATTTAGG	219249
rs30264767	snp	A/G	0.375	0.216506	intron-variant	Tdrd3	Mm_Celera	14:87517767	CTTTGATAAGTTAGT[A/G]TCTGTATGAGTGCTA	219249
rs30271730	snp	A/G	0.49827	0.0293608	intron-variant	Tdrd3	Mm_Celera	14:87492109	GTGGGAGCAGAGTGA[A/G]GAGGATGCTGAGGGA	219249
rs30274061	snp	C/T	0.444444	0.157135	intron-variant	Tdrd3	Mm_Celera	14:87488040	CCACTCCTGCCTCCC[C/T]GCCCTAGCATTCCCC	219249
rs30287755	snp	A/G	0.5	0	intron-variant, nc-transcript-variant	Tdrd3, Gm33076	GRCm38.p3	14:87533086	AAGAAAACCTTAGCG[A/G]TGTTAGTCCGCACAG	219249
rs30292111	snp	A/G	0.444444	0.157135	intron-variant	Tdrd3	Mm_Celera	14:87492255	TGATTTCAGGCTATC[A/G]GTGATTTAAAAACTA	219249
rs30298686	snp	A/T	0.48	0.0979796	intron-variant	Tdrd3	Mm_Celera	14:87436019	AACTCCAAACGTGAA[A/T]CAGTAGCACCTGCTC	219249
rs30298887	snp	G/T	0.345679	0.230967	intron-variant	Tdrd3	Mm_Celera	14:87424605	GATTCTAGTTTTCAG[G/T]CTTACACACATGAAT	219249
rs30301102	snp	A/G	0.375	0.216506	intron-variant	Tdrd3	Mm_Celera	14:87483648	AGACAATTTGGGTGT[A/G]TGTCATGGGTAAGGG	219249
rs30304310	snp	A/G	0.486111	0.0821678	intron-variant	Tdrd3	Mm_Celera	14:87460673	TAAGTATGTTTTTTA[A/G]ATTAAACATTAGCTG	219249
rs30308235	snp	A/G	0.375	0.216506	intron-variant	Tdrd3	Mm_Celera	14:87485969	TAAGAGCTTATTCTA[A/G]TATAGCATAAGCTTT	219249
rs30308553	snp	C/T	0.497041	0.0383476	intron-variant	Tdrd3	Mm_Celera	14:87511001	TCACACTGATTTCCA[C/T]GTTATAGAGAAGTTT	219249
rs30309035	snp	C/T	0.493827	0.0552116	intron-variant	Tdrd3	Mm_Celera	14:87494379	ATTTGGTTTGCAGCT[C/T]AGCTCTTTCTATGCA	219249
rs30315555	snp	A/G	0.444444	0.157135	missense, nc-transcript-variant	Tdrd3	Mm_Celera	14:87506023	CAGAAGAGAGGATCA[A/G]GTGTGACAGGCCATA	219249
rs30318497	snp	C/T	0.484429	0.0868505	downstream-variant-500B, intron-variant	Tdrd3	Mm_Celera	14:87515302	AAGATAGTTGATGCA[C/T]TATGGAAAATACATG	219249
rs30334404	snp	A/G	0.444444	0.157135	intron-variant	Tdrd3	Mm_Celera	14:87426660	GGAGTTTTGAAGGGG[A/G]AAAGCATATGCTAAG	219249
rs30338134	snp	G/T	0.498615	0.0262793	intron-variant	Tdrd3	Mm_Celera	14:87492635	GTTGATGGAGAGGGG[G/T]CAGAGACTGTGCTAG	219249
rs30349569	snp	A/G	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87422199	TCTGGCTGCCAGCCT[A/G]GATCTTGCTGTGTAG	219249
rs30363450	snp	C/T	0.444444	0.157135	intron-variant	Tdrd3	Mm_Celera	14:87462330	AATATTAAGACATGT[C/T]CTATGGGCGTGTGGT	219249
rs30376895	snp	A/G	0.375	0.216506	intron-variant	Tdrd3	Mm_Celera	14:87423049	GGCCTAGTATGTACT[A/G]TAACCTCAGTAGGGT	219249
rs30383032	snp	A/T	0.5	0	intron-variant	Tdrd3	GRCm38.p3	14:87527516	TGATTTGTGTTCTAT[A/T]TTAAGAAATTTAGCT	219249
rs30383196	snp	C/T	0.484429	0.0868505	intron-variant	Tdrd3	Mm_Celera	14:87523178	GTGAGAATTATGATG[C/T]TTTAAGATTTCAGTC	219249
rs30383393	snp	A/G	0.444444	0.157135	intron-variant	Tdrd3	Mm_Celera	14:87431028	GATGGGAGTTGAGAA[A/G]TTCATTAATCTCTGT	219249
rs30385006	snp	C/T	0.444444	0.157135	intron-variant	Tdrd3	Mm_Celera	14:87426717	GTGTAGATTTGGCTA[C/T]GTGTCCTGTGTTTGA	219249
rs30388828	snp	A/G	0.359862	0.224567	intron-variant	Tdrd3	Mm_Celera	14:87459677	GCTGAATTTGACTTG[A/G]TCTCTGAACTATCCC	219249
rs30389597	snp	A/C	0.498615	0.0262793	intron-variant	Tdrd3	Mm_Celera	14:87486378	CCAGCAAGATATGGG[A/C]AGGACCAAGGCCAAG	219249
rs30401584	snp	C/T	0.432133	0.171253	intron-variant, nc-transcript-variant	Tdrd3, Gm33076	Mm_Celera	14:87533268	GGCTGTCACTCTGTG[C/T]TACAATGTTGTCCTT	219249
rs30424996	snp	A/G	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87511182	GAAGATAGAAGCCAG[A/G]CGAATTGAATCCTGC	219249
rs30431148	snp	G/T	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87441003	AAGATATTAGGTGTA[G/T]TCTCCCAGGGACAGG	219249
rs30432689	snp	A/G	0.5	0	intron-variant	Tdrd3	Mm_Celera	14:87483965	TCGGGAGTTGCAGTT[A/G]TTTTAAATCCTTGAA	219249
rs30433063	snp	G/T	0.33241	0.236027	intron-variant	Tdrd3	Mm_Celera	14:87538730	CTGAATTAATTTTTA[G/T]AAAGCACACACAGAG	219249
rs30442105	snp	C/T	0.475309	0.108333	intron-variant	Tdrd3	Mm_Celera	14:87523647	GACGATTTTTATCAC[C/T]GTGGGCTTGGCCTCC	219249
rs30442203	snp	C/T	0.459184	0.136902	intron-variant	Tdrd3	Mm_Celera	14:87487298	GGAAGGTAGGCTAAC[C/T]TGAAAACAACATTAA	219249

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