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
rs4036	snp	A/G	0.20752	0.246364	utr-variant-3-prime, downstream-variant-500B, missense	TCEB2, SRRM2	GRCh38.p7	16:2771524	TCTTGGGGTTCCCTC[A/G]TTGAACATGCTGTCA	6923
rs8017	snp	C/T	0.499352	0.0179917	utr-variant-3-prime, downstream-variant-500B, missense	TCEB2, SRRM2	GRCh38.p7	16:2771572	CAGCTTGTGTTTCTG[C/T]TCTTGGCCATCGTCT	6923
rs8843	snp	A/G	0.0107246	0.0724382	intron-variant, utr-variant-3-prime, nc-transcript-variant	TCEB2, SRRM2	GRCh38.p7	16:2771250	TATAAGGTGTTCTTG[A/G]AAGGAAGGGGCAGGA	6923
rs916947	snp	A/G	0.415891	0.18703	intron-variant	TCEB2	GRCh38.p7	16:2774983	ACCAGGCTCTATGCT[A/G]TGTATCACCGAAACC	6923
rs1050195	snp	C/T	0	0	intron-variant, utr-variant-3-prime, nc-transcript-variant	TCEB2, SRRM2	GRCh38.p7	16:2771334	CAACTTTTCATGTTT[C/T]TTAAAGGCATTTTGG	6923
rs1058855	snp	C/G	0.412416	0.190055	utr-variant-3-prime, downstream-variant-500B, intron-variant	TCEB2, SRRM2	GRCh38.p7	16:2771762	GACCTGGGTTGCCCT[C/G]AGACCCAAGCCATTG	6923
rs2009509	snp	C/G	0.48155	0.0942576	intron-variant	TCEB2	GRCh38.p7	16:2774929	ATTTGGATTTTGCCA[C/G]TTTTCAGGTTCAGTA	6923
rs2285877	snp	C/T	0.411914	0.190483	intron-variant	TCEB2	GRCh38.p7	16:2772173	CTGCAGATGATCACA[C/T]GTGAACACCAAGGCC	6923
rs2335454	snp	C/G	0.471863	0.115225	upstream-variant-2KB	TCEB2	GRCh38.p7	16:2778156	GAGAGAGGGGTGGAA[C/G]GTGGAGGTGCGATTT	6923
rs2335455	snp	C/T	0.459004	0.137176	upstream-variant-2KB	TCEB2	GRCh38.p7	16:2778172	GTGGAGGTGCGATTT[C/T]TGCCTCGGCATCTAG	6923
rs3066059	in-del	-/TTG			upstream-variant-2KB	TCEB2	GRCh38.p7	16:2778363	TAATTCTAGTTATTG[-/TTG]CTACTTTTGACTTGT	6923
rs3094772	snp	C/T	0.441295	0.160954	intron-variant	TCEB2	GRCh38.p7	16:2775815	CCTATCTCCAGATAG[C/T]TCAGTGGCTCCTCAA	6923
rs3094774	snp	C/T	0.328497	0.237357	intron-variant	TCEB2	GRCh38.p7	16:2775593	TTGGGACTTGCCCCA[C/T]GTAGGGCCTCTCCCA	6923
rs3094776	snp	A/T	0.409382	0.192607	intron-variant	TCEB2	GRCh38.p7	16:2775275	CATTTTTTTTTTTTT[A/T]AAAAAGAAGCAACCA	6923
rs3094782	snp	C/T	0.452103	0.147154	intron-variant	TCEB2	GRCh38.p7	16:2774187	GCTGGAGTGCAGTGG[C/T]GCCATCTCAGCCCAC	6923
rs3094784	snp	A/T	0.416708	0.186302	intron-variant	TCEB2	GRCh38.p7	16:2774025	TCAGGCTGGTCTCAA[A/T]CTCCTGACCTCAGGC	6923
rs3094785	snp	C/G	0.416545	0.186448	intron-variant	TCEB2	GRCh38.p7	16:2773767	TGCAGATGAGAAAAT[C/G]AAGGCTAAGGAAGGT	6923
rs3094789	snp	C/G	0.426966	0.176587	intron-variant	TCEB2	GRCh38.p7	16:2772835	AGAGAGCCAGAGCCT[C/G]AGAGCGTGGGAAGCA	6923
rs3112684	snp	C/T	0.416708	0.186302	intron-variant	TCEB2	GRCh38.p7	16:2773138	CCCACAGCTTTTCTC[C/T]TGTGCTTTCTTCCAG	6923
rs3112685	snp	C/T	0.0349115	0.127424	intron-variant	TCEB2	GRCh38.p7	16:2773265	GGGGAGGTGGGGTGC[C/T]CCAGCGCTATCTAGT	6923
rs3112686	snp	C/T	0.416055	0.186885	intron-variant	TCEB2	GRCh38.p7	16:2773569	GGAACAACATGATGA[C/T]GGGTTGAGCTGCACC	6923
rs3112687	snp	C/T	0.416382	0.186593	intron-variant	TCEB2	GRCh38.p7	16:2773922	GCTCTTGGCACTCCC[C/T]TGCTCTCTTCAGACA	6923
rs3112688	snp	C/T	0.416708	0.186302	intron-variant	TCEB2	GRCh38.p7	16:2774539	CCTAGCCTGAACTTA[C/T]GGAACGGAAAGGTGG	6923
rs3214191	in-del	-/G	0.439031	0.163607	utr-variant-3-prime, intron-variant	TCEB2	GRCh38.p7	16:2771988	AAGCCGTGCAGTGAG[-/G]ACCCCCAAGAGGCCC	6923
rs5815134	in-del	-/G	0.45235	0.146814	intron-variant	TCEB2	GRCh38.p7	16:2774821	TCTAAAGCTTGGGCA[-/G]GGGTGGGGTATGGCT	6923
rs7192849	snp	C/T	0.000340086	0.0130356	utr-variant-3-prime, intron-variant	TCEB2	GRCh38.p7	16:2771956	CAGACTCCCAAATCT[C/T]TTTTATTGGGGGAAA	6923
rs9888947	snp	A/C			intron-variant	TCEB2	GRCh38.p7	16:2772537	atctctactaaaaat[A/C]caaaaaaaaaaaaaa	6923
rs9925824	snp	A/G	0.472709	0.11358	upstream-variant-2KB	TCEB2	GRCh38.p7	16:2777972	GCATCGCCCCAAGTT[A/G]CATTTACATGAGAGT	6923
rs9928614	snp	A/G	0	0	intron-variant	TCEB2	GRCh38.p7	16:2776331	CCAGCTCTAGAATCT[A/G]AACAATGCACTTGGG	6923
rs11551731	snp	A/G			intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	TCEB2, SRRM2	GRCh38.p7	16:2771023	TTTCACAGGAACAAA[A/G]AAAAAAAAAAGGGGA	6923
rs11552264	snp	A/C			synonymous-codon	TCEB2	GRCh38.p7	16:2777095	CCGGCGCCACAAGAC[A/C]ACCATCTTCACGGAC	6923
rs11552265	snp	A/G			synonymous-codon	TCEB2	GRCh38.p7	16:2772050	CAGCCCGCCAGAGCT[A/G]CCCGATGTGATGAAG	6923
rs11552266	snp	A/G			synonymous-codon	TCEB2	GRCh38.p7	16:2775470	GGCCCCAGCCACAGT[A/G]GGGCTGGCCTTCCGG	6923
rs11552267	snp	C/G			missense	TCEB2	GRCh38.p7	16:2777063	CCAAGGAGTCCAGCA[C/G]GGTGTTCGAACTGAA	6923
rs11646257	snp	A/T	0	0	intron-variant	TCEB2	GRCh38.p7	16:2773170	TAGGAGACCCATCTC[A/T]GCTTGGCTCAGggtt	6923
rs12925110	snp	A/G	0.247905	0.249991	intron-variant	TCEB2	GRCh38.p7	16:2774696	AAAACACAGCTCTAT[A/G]ACCTCTCTTCAAGTT	6923
rs34102909	in-del	-/G			upstream-variant-2KB	TCEB2	GRCh38.p7	16:2778030	GCAGAGACACCCCAG[-/G]CTGGGTCGTGCTGGG	6923
rs34213102	snp	C/G	0.248755	0.249997	intron-variant	TCEB2	GRCh38.p7	16:2774211	CTCCAGCCTAGACAA[C/G]GGAGTGCGACTCTGT	6923
rs34426974	in-del	-/G			intron-variant	TCEB2	GRCh38.p7	16:2774213	CAGCCTAGACAACGG[-/G]AGTGCGACTCTGTCT	6923
rs34923755	in-del	-/G			intron-variant	TCEB2	GRCh38.p7	16:2774089	CAAAGATTAGCTGGG[-/G]CGTGGTGGCACATGC	6923
rs34936144	in-del	-/A	0	0	intron-variant	TCEB2	GRCh38.p7	16:2772560	AAAAAAAAAAAAAAA[-/A]TTAGCCGGGCATGGT	6923
rs34944074	in-del	-/TCT	0	0	intron-variant	TCEB2	GRCh38.p7	16:2772858	GGCTCTCTATGTTCT[-/TCT]GTAAGTTCTTTCCTA	6923
rs35716651	in-del	-/C			intron-variant	TCEB2	GRCh38.p7	16:2774882	AGATGTGGCAGTCCC[-/C]AGCAGATGACCTAAC	6923
rs58283332	snp	A/G	0.00760445	0.0611915	intron-variant	TCEB2	GRCh38.p7	16:2775648	GGAAGTCAGAGGAGG[A/G]AAGAGAGAGTTCCCT	6923
rs63744561	snp	G/T	0.458775	0.137524	upstream-variant-2KB	TCEB2	GRCh38.p7	16:2778171	GGTGGAGGTGCGATT[G/T]TTGCCTCGGCATCTA	6923
rs66684270	in-del	AG/C	0.5	0	intron-variant	TCEB2	GRCh38.p7	16:2774211	CTCCAGCCTAGACAA[AG/C]GGAGTGCGACTCTGT	6923
rs73474764	snp	A/G	0.0244538	0.107838	intron-variant	TCEB2	GRCh38.p7	16:2775312	CAAACACATTGTGAA[A/G]GGATATTGCCAGCCC	6923
rs73474767	snp	A/G	0.118933	0.212888	intron-variant	TCEB2	GRCh38.p7	16:2776597	AAGGAGTGTCCGGGG[A/G]GACAGCGTGATTCCG	6923
rs73496400	snp	A/C/G	0.0241781	0.107266	intron-variant	TCEB2	GRCh38.p7	16:2772115	CATCTGTGGAGGAAG[A/C/G]AGCAGAGCTGCAGGG	6923
rs73496401	snp	A/C/G	0.0245261	0.107994	intron-variant	TCEB2	GRCh38.p7	16:2772128	AGCAGCAGAGCTGCA[A/C/G]GGGGGTATTCCAGCT	6923
rs73496402	snp	C/G	0.0825414	0.185628	intron-variant	TCEB2	GRCh38.p7	16:2772718	TCAAAAAAAAAAAAT[C/G]AAACTAGACTATCTA	6923
rs73498307	snp	A/C	0.5	0	intron-variant	TCEB2	GRCh38.p7	16:2773291	CTAGTGGGTAGAGGC[A/C]TGGGATACGGCTCCA	6923
rs74340202	snp	G/T			utr-variant-3-prime, intron-variant	TCEB2	GRCh38.p7	16:2771987	TGGGCCTCTTGGGGG[G/T]CCTCACTGCACGGCT	6923
rs74349088	snp	C/G	0.00318978	0.0398085	intron-variant	TCEB2	GRCh38.p7	16:2772927	AATGGCTGGCTGCTT[C/G]TGGACTTTCAGGGTC	6923
rs74788235	snp	A/G	0.00119737	0.0244387	intron-variant	TCEB2	GRCh38.p7	16:2774990	GTGATACATAGCATA[A/G]AGCCTGGTATGATGT	6923
rs75028454	snp	C/T	0.00993419	0.0697739	intron-variant	TCEB2	GRCh38.p7	16:2775767	TGGGACTTTAGAATC[C/T]GGTTTTATCCAAATT	6923
rs75586278	snp	G/T	0.0123036	0.0774623	intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	TCEB2, SRRM2	GRCh38.p7	16:2771114	ATGCAGATGGGAGTT[G/T]GGGGAGGGGAGGATA	6923
rs76132205	snp	C/T	0.00993419	0.0697739	intron-variant	TCEB2	GRCh38.p7	16:2773093	TTCCCTGTCTTGTCC[C/T]TACTGTCACCCCAAC	6923
rs76369032	snp	G/T			missense	TCEB2	GRCh38.p7	16:2776998	GACGAGCAGCGGCTG[G/T]ACAAGGTGGGTCCCG	6923
rs76875659	snp	C/G	0.0103295	0.0711199	utr-variant-3-prime, downstream-variant-500B	TCEB2, SRRM2	GRCh38.p7	16:2771415	AGAAATGCAGGAACT[C/G]GGTCTGTAGACTGTT	6923
rs77177311	snp	C/T	0.0123036	0.0774623	intron-variant	TCEB2	GRCh38.p7	16:2776330	TCCAGCTCTAGAATC[C/T]GAACAATGCACTTGG	6923
rs77319255	snp	A/G	0.00159617	0.0282053	intron-variant	TCEB2	GRCh38.p7	16:2775044	GTCAGCATCCTAACC[A/G]TGGCTCCCTACGTGA	6923
rs77657733	snp	A/G	0.0119091	0.0762411	intron-variant	TCEB2	GRCh38.p7	16:2774370	CATCTGTTGGGCACT[A/G]GCAGCAGGCCAGACC	6923
rs78044346	snp	A/G	0.5	0	upstream-variant-2KB	TCEB2	GRCh38.p7	16:2777728	CTGCTGTTGGGCTTA[A/G]GGATGGCCCGGGCGA	6923
rs78292378	snp	C/T	0.000141513	0.00841049	utr-variant-3-prime, intron-variant	TCEB2	GRCh38.p7	16:2771988	GGGCCTCTTGGGGGT[C/T]CTCACTGCACGGCTT	6923
rs78617860	snp	C/T	0.0140508	0.0826316	intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	TCEB2, SRRM2	GRCh38.p7	16:2771022	CTCCCCTTTTTTTTT[C/T]CTTTGTTCCTGTGAA	6923
rs78880023	snp	A/T	0.0107246	0.0724382	intron-variant	TCEB2	GRCh38.p7	16:2776546	GAGTGGGACCTGACT[A/T]TCTTTGCATTCACTG	6923
rs79638577	snp	A/C	0.000197697	0.00994029	utr-variant-3-prime, downstream-variant-500B, missense	TCEB2, SRRM2	GRCh38.p7	16:2771597	TCGTCTGGGAGTGGA[A/C]ATGCAGGCTATGGGG	6923
rs79886307	snp	C/T	0.000691654	0.0185836	utr-variant-3-prime, downstream-variant-500B, missense	TCEB2, SRRM2	GRCh38.p7	16:2771507	GGACCTGTGTGGGTC[C/T]GTCTTGGGGTTCCCT	6923
rs111748580	snp	A/G	0.5	0	intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	TCEB2, SRRM2	GRCh38.p7	16:2771099	TTGGGGTGGGAGGGA[A/G]TGCAGATGGGAGTTG	6923
rs111815759	in-del	-/C/G	7.07139e-05	0.00594575	intron-variant	TCEB2	GRCh38.p7	16:2772127	AGCAGCAGAGCTGCA[-/C/G]GGGGGGTATTCCAGC	6923
rs111838652	snp	A/G	0.5	0	intron-variant	TCEB2	GRCh38.p7	16:2776346	GAACAATGCACTTGG[A/G]CGACAACCTCACAAT	6923
rs112074102	snp	C/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	TCEB2, SRRM2	GRCh38.p7	16:2771152	GGATACCCCAGCCTG[C/G]AGTCAGGGCCAGGGA	6923
rs113014227	snp	C/T	0.0729998	0.176553	intron-variant	TCEB2	GRCh38.p7	16:2772588	GGTGGCGGGCACCTA[C/T]AGTCCCAGCTTCTCG	6923
rs113444190	snp	A/T			splice-acceptor-variant	TCEB2	GRCh38.p7	16:2777129	ATGAGGAACACGTCC[A/T]GGGGGCGGCGGGCCG	6923
rs113808096	snp	A/C	0.5	0	intron-variant	TCEB2	GRCh38.p7	16:2773126	ACAGCAAACAAACCC[A/C]CAGCTTTTCTCCTGT	6923
rs114055328	snp	A/G	0.00993419	0.0697739	intron-variant	TCEB2	GRCh38.p7	16:2772786	CCCATCATGACCTGA[A/G]TACCACCAAGTCCTT	6923
rs114353713	snp	A/T	0.00993419	0.0697739	intron-variant	TCEB2	GRCh38.p7	16:2772957	CCAACTCAGGTCACC[A/T]CCTCAGATGAACCTC	6923
rs114543103	snp	C/T	0.0123036	0.0774623	upstream-variant-2KB	TCEB2	GRCh38.p7	16:2778176	AGGTGCGATTTTTGC[C/T]TCGGCATCTAGAGAG	6923
rs114919702	snp	A/C	0.0130921	0.0798413	upstream-variant-2KB	TCEB2	GRCh38.p7	16:2778237	ACTGTGGCCATGGGC[A/C]GTTAACCTCATCAAA	6923
rs114920757	snp	C/T	0.00676609	0.0577691	intron-variant	TCEB2	GRCh38.p7	16:2772452	TCCCTTCACACACTT[C/T]GGGAGGCCGAGACGG	6923
rs115550678	snp	C/T	0.0479149	0.147179	upstream-variant-2KB	TCEB2	GRCh38.p7	16:2777394	CGCCATTTTAAGTGA[C/T]CTGGAAGCGGGCGGT	6923
rs116010376	snp	A/G	0.00835141	0.0640778	upstream-variant-2KB	TCEB2	GRCh38.p7	16:2778516	ACCTGTCTCTTCTTC[A/G]TGACGTGAGTCATGA	6923
rs116130595	snp	A/T	0.0569829	0.158885	intron-variant	TCEB2	GRCh38.p7	16:2775159	CAGTGGAAGCCACAC[A/T]CAGAGTAACATGCAG	6923
rs116313732	snp	A/C	0.0733688	0.176922	intron-variant	TCEB2	GRCh38.p7	16:2774543	GCCTGAACTTATGGA[A/C]CGGAAAGGTGGAGCT	6923
rs116345411	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	TCEB2	GRCh38.p7	16:2779251	CAAACCCCAGCTCCT[A/G]CCGGCAAAGCCCGGG	6923
rs116444725	snp	A/G	0.00993419	0.0697739	intron-variant	TCEB2	GRCh38.p7	16:2772993	CACGCACCCCCAAAA[A/G]TCAAGACATCCTGAC	6923
rs116768536	snp	A/G	0.0130921	0.0798413	intron-variant	TCEB2	GRCh38.p7	16:2773991	TCCCAGCACTTTGGG[A/G]GGCTGGGATGTATGG	6923
rs116928678	snp	C/T	1.69746e-05	0.00291325	intron-variant, utr-variant-3-prime, nc-transcript-variant	TCEB2, SRRM2	GRCh38.p7	16:2771381	CAGCAAGAGCAACTT[C/T]TTCTGTCAAATAAAA	6923
rs117834573	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB	TCEB2	GRCh38.p7	16:2778216	CAGCCCTGGGCTCCG[C/T]TGCTGACTGTGGCCA	6923
rs117842792	snp	C/T	0.00358779	0.0422022	intron-variant	TCEB2	GRCh38.p7	16:2774416	CTCAACACCACCTTG[C/T]TGTGAAGCCAGTCTC	6923
rs118113051	snp	G/T	0.0178098	0.0926698	intron-variant	TCEB2	GRCh38.p7	16:2776588	CTCCACCCGAAGGAG[G/T]GTCCGGGGGGACAGC	6923
rs138251122	in-del	-/A	0.248755	0.249997	intron-variant	TCEB2	GRCh38.p7	16:2774208	CTCCAGCCTAGACAA[-/A]CGGAGTGCGACTCTG	6923
rs138264981	snp	C/G	0.00557542	0.0525036	intron-variant	TCEB2	GRCh38.p7	16:2775153	ACAGGGCAGTGGAAG[C/G]CACACACAGAGTAAC	6923
rs138405434	snp	A/G/T	0.000428277	0.0146278	utr-variant-3-prime, downstream-variant-500B, missense, stop-gained	TCEB2, SRRM2	GRCh38.p7	16:2771588	TCTTGGCCATCGTCT[A/G/T]GGAGTGGACATGCAG	6923
rs138732435	snp	C/T	6.70455e-05	0.00578949	missense	TCEB2	GRCh38.p7	16:2775535	CGCCCAGTGTCTTGC[C/T]ATCATCCAAGAGTTG	6923
rs138809828	snp	C/T	0.000798403	0.0199641	intron-variant	TCEB2	GRCh38.p7	16:2775827	TGAGCTATCTGGAGA[C/T]AGGCAGACCTGGCTT	6923
rs138948846	snp	C/T	0.00161182	0.0283427	intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	TCEB2, SRRM2	GRCh38.p7	16:2771007	GAGGGCTCCCTTTCC[C/T]TCCCCTTTTTTTTTT	6923
rs139350354	snp	A/C	0.000912888	0.021345	utr-variant-3-prime, intron-variant	TCEB2	GRCh38.p7	16:2771948	CAACCAGGCAGACTC[A/C]CAAATCTCTTTTATT	6923
rs139427741	snp	C/T	0.000399281	0.0141238	intron-variant	TCEB2	GRCh38.p7	16:2773166	CAGCTAGGAGACCCA[C/T]CTCTGCTTGGCTCAG	6923

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