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
rs173041	snp	A/G			intron-variant, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55172838	TACGACCAGGGCTTA[A/G]AGTTTCGTACCACCT	166979
rs173042	snp	G/T	0	0	missense, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55172979	CCCTCCGAGGCGCGG[G/T]GCGCTCCAGTTTCCA	166979
rs182858	snp	A/G	0.490007	0.0699769	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137248	TAATTGCCTGTGGCA[A/G]TTTCTAGAAGGTCCT	166979
rs186762	snp	A/G	0	0	intron-variant	CDC20B	GRCh38.p7	5:55135248	tctttctctctctGT[A/G]TATATATATATATAG	166979
rs191396	snp	G/T	0.289039	0.246933	intron-variant	CDC20B	GRCh38.p7	5:55143685	TCAAAGTGATTATCT[G/T]GTTTTAAAAACCAAA	166979
rs193104	snp	G/T	0	0	intron-variant	CDC20B	GRCh38.p7	5:55131457	ttttttgctgatttg[G/T]gtttctcttccattt	166979
rs193105	snp	C/T	0.299916	0.244966	intron-variant, downstream-variant-500B	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55170174	GACTTCACTGAAAAT[C/T]TGGGGACACATTGTA	166979
rs233625	snp	A/G	0.48178	0.0936921	intron-variant	CDC20B	GRCh38.p7	5:55157548	TTTGAAAACTTACGT[A/G]TATATCTCCTGTCAA	166979
rs336061	snp	A/G	0	0	intron-variant	CDC20B	GRCh38.p7	5:55120340	AGAGAAAGAGAGCTT[A/G]TTGGGGGCATAGGCT	166979
rs336062	snp	C/T	0.282105	0.24793	intron-variant	CDC20B	GRCh38.p7	5:55121058	GTTCAGAAAATAAAA[C/T]TGCCTTCTATTTATT	166979
rs336071	snp	A/T	0.261608	0.24973	intron-variant	CDC20B	GRCh38.p7	5:55146202	ctgaagctcagcttc[A/T]gtgattggcggagac	166979
rs336072	snp	A/G	0.26078	0.249767	intron-variant	CDC20B	GRCh38.p7	5:55145737	agaggaggaggagga[A/G]gaagaAAGAAGAAAG	166979
rs336073	snp	C/T	0.480931	0.0957637	intron-variant	CDC20B	GRCh38.p7	5:55144757	TGTATATAACTGTGA[C/T]GATTGTCAGTACTAG	166979
rs336074	snp	G/T	0.280328	0.248154	intron-variant	CDC20B	GRCh38.p7	5:55144191	TTCTGCAATAGAAAG[G/T]GGGAGAGAGGCAAAG	166979
rs336075	snp	A/G	0.26078	0.249767	intron-variant	CDC20B	GRCh38.p7	5:55144122	CAAAGCAAGCATCCC[A/G]TAATGTTTTCCTTGC	166979
rs336076	snp	A/G	0.481087	0.0953875	intron-variant	CDC20B	GRCh38.p7	5:55144064	CCATAGTTTTAAATG[A/G]TAGTGGAAAGAGTAT	166979
rs336077	snp	C/T	0.262159	0.249704	intron-variant	CDC20B	GRCh38.p7	5:55141562	tgtttacattcttcg[C/T]gactcagtgagtata	166979
rs336078	snp	A/G	0.262159	0.249704	intron-variant	CDC20B	GRCh38.p7	5:55141069	aacatGACCTTTGGC[A/G]TAGTTCTGAACCTGA	166979
rs336079	snp	C/T	0.282632	0.247861	intron-variant	CDC20B	GRCh38.p7	5:55138225	TGTAGTGAGCCGAAA[C/T]CACGCCACTGCACTC	166979
rs336080	snp	C/T	0.282632	0.247861	intron-variant	CDC20B	GRCh38.p7	5:55137776	CTATATTCACTCCCA[C/T]AGTGTTTGTTCTTGT	166979
rs336081	snp	C/T	0.488184	0.0759499	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137565	GACTAATTGAGAGGC[C/T]CTCTGAATACTCTAT	166979
rs336082	snp	A/G	0.299664	0.245017	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159611	GGCAATCAAATACCA[A/G]GTGAATACAGTCAAA	166979
rs336083	snp	A/T	0.481473	0.0944461	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159189	GTCTCTAAAAAAGAA[A/T]TTTAATTAGCTGGTT	166979
rs336084	snp	A/T	0.299916	0.244966	intron-variant	CDC20B	GRCh38.p7	5:55156954	ATATGAGAACACACA[A/T]GAAACGGAAGGATTA	166979
rs336085	snp	A/G	0.471673	0.115589	intron-variant	CDC20B	GRCh38.p7	5:55156046	GCCATGTGGAACTGT[A/G]AGTCCATTAAATCTC	166979
rs336086	snp	A/T			intron-variant	CDC20B	GRCh38.p7	5:55154852	actaacaaatgagta[A/T]ttaaatacaatttat	166979
rs336087	snp	A/G	0.471004	0.116864	intron-variant	CDC20B	GRCh38.p7	5:55154174	ccttggatgtgctgg[A/G]gtgttgtcccattac	166979
rs336088	snp	C/T	0.278133	0.248412	intron-variant	CDC20B	GRCh38.p7	5:55152425	aataaacactccctc[C/T]gattcatatatccca	166979
rs336089	snp	C/T	0.330249	0.23677	intron-variant	CDC20B	GRCh38.p7	5:55149445	tgatgagtgtttggg[C/T]tgtctgcaccttctt	166979
rs336090	snp	C/T	0.262159	0.249704	intron-variant	CDC20B	GRCh38.p7	5:55148673	tctcactttgtcgcc[C/T]aggctggagtgcagc	166979
rs336099	snp	C/G	0.325799	0.238232	intron-variant, downstream-variant-500B	CDC20B	GRCh38.p7	5:55135984	tgctctctagcttgg[C/G]tgacagagtgagact	166979
rs336100	snp	C/T	0.326035	0.238157	intron-variant	CDC20B	GRCh38.p7	5:55135012	cattagagttcattc[C/T]tgatgttatgtattc	166979
rs336101	snp	A/G	0.33875	0.233717	intron-variant	CDC20B	GRCh38.p7	5:55134373	GCAGTTTTGCCCTCA[A/G]CTACAGGTTTTCATA	166979
rs336102	snp	A/G	0.282632	0.247861	intron-variant	CDC20B	GRCh38.p7	5:55134146	GTTTGAACTTAGTAT[A/G]GTCTTTTGATGAGAA	166979
rs336103	snp	A/G	0.282632	0.247861	intron-variant	CDC20B	GRCh38.p7	5:55131360	GTTCTATTTTAATTG[A/G]TCTTAGCTTTTTGGC	166979
rs336104	snp	G/T			intron-variant	CDC20B	GRCh38.p7	5:55131327	TATCTCTTTGTATTG[G/T]GTTTTGTCGTCATTT	166979
rs336105	snp	A/G	0.490007	0.0699769	intron-variant	CDC20B	GRCh38.p7	5:55130447	gagaaCCCCATGGTC[A/G]CCTTGTTATCCTGCT	166979
rs336106	snp	A/G	0.489434	0.0719116	intron-variant	CDC20B	GRCh38.p7	5:55130420	TGCTTCTAAGACCTG[A/G]CTCTACTTACACATA	166979
rs336114	snp	C/T	0.277867	0.248442	intron-variant	CDC20B	GRCh38.p7	5:55167894	Taaattagccaggtg[C/T]ggtagcacacacctg	166979
rs336115	snp	C/T	0.446902	0.154045	utr-variant-5-prime, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173093	GTCTTGACGCCTAAT[C/T]GTCAAACCCCTGGAG	166979
rs336116	snp	A/G	0.438386	0.164349	upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55174247	TTTTTTTTTTTTTTG[A/G]ATCACTGACCCTTTT	166979
rs368003	snp	A/G	0	0	intron-variant, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55172794	AACTAGGCACCTTCA[A/G]AATATAACTAAATTA	166979
rs369527	snp	A/G			upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159266	actttgggaggccta[A/G]atgggaggatcactt	166979
rs381852	snp	C/T	0.308378	0.243088	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55164133	ATGGGCTCCTCTGGC[C/T]TCCAGAACTTCACAA	166979
rs382402	snp	G/T	0.322607	0.239224	synonymous-codon	CDC20B	GRCh38.p7	5:55124971	AGCCCAGCATCATGT[G/T]GGAACACTTCGCCAC	166979
rs384818	snp	C/T	0.289683	0.24683	intron-variant	CDC20B	GRCh38.p7	5:55115997	AGGGGCCTGCATTGT[C/T]GTTATAAATGTAAAC	166979
rs389075	snp	C/T	0.336017	0.234736	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113759	CTTGAAAAACACTTA[C/T]TAAAATCTCACTATA	166979
rs390074	snp	G/T			intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137205	ATTTGGAGCTCTCAG[G/T]GCtttctttcttttt	166979
rs391112	snp	G/T	0.281841	0.247964	intron-variant	CDC20B	GRCh38.p7	5:55117261	GTCATGATTTTTTTT[G/T]GGGGGAAAATTTCAG	166979
rs396335	snp	C/T	0.0711525	0.174681	downstream-variant-500B	CDC20B	GRCh38.p7	5:55112678	TAATTTGTCAATATA[C/T]ATTTTTATTTTTCCT	166979
rs402018	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55153165	tggaacctttgcctt[C/T]tgggcttaagccatc	166979
rs403881	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55153236	atagccagaccttgt[C/T]tcataaaaaaaaaaa	166979
rs409095	snp	A/G	0.390651	0.206682	intron-variant	CDC20B	GRCh38.p7	5:55139704	CATCAGTTTCTCGAC[A/G]TGCTTATATCACACT	166979
rs417992	snp	C/T	0.323197	0.239044	intron-variant	CDC20B	GRCh38.p7	5:55139707	GTGATATAAGCATGT[C/T]GAGAAACTGATGAAA	166979
rs423074	snp	C/T	0	0	missense, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55172952	CCCACAGCATCTCCT[C/T]TTCCGTGCGGACCCT	166979
rs423451	snp	A/G	0	0	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162322	aatcgcttgaaccca[A/G]aggcagaggttgcag	166979
rs424203	snp	A/G	0.376195	0.215812	intron-variant	CDC20B	GRCh38.p7	5:55116469	ATTTATTTATTTTGA[A/G]ACAGGGTCTCACTCT	166979
rs426722	snp	G/T	0	0	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162126	aaaggccgggcgcgg[G/T]ggctcacgcctgtaa	166979
rs433328	snp	A/T	0.34303	0.232046	intron-variant	CDC20B	GRCh38.p7	5:55123737	AAACAAAACAAAAAA[A/T]TAGTTGAAAACCCAA	166979
rs434658	snp	A/G	0.481932	0.0933148	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163076	tttgaagcacggagc[A/G]tacattaatctggca	166979
rs436282	snp	C/T	0.481932	0.0933148	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162935	aggcccgtatatcaa[C/T]cctggctcaaccact	166979
rs444527	snp	C/T	0.321308	0.239615	missense	CDC20B	GRCh38.p7	5:55114271	AGTCCAGACCAGACC[C/T]GGGTGTTTTCTGCTG	166979
rs903887	snp	C/T	0.282632	0.247861	intron-variant	CDC20B	GRCh38.p7	5:55125463	TTAGATATTTATTTC[C/T]TTTTTCTATGTCTAA	166979
rs903888	snp	C/G	0.297382	0.245469	intron-variant	CDC20B	GRCh38.p7	5:55125344	CCTGTATATAAACTA[C/G]TCTTTGGGAAAATCT	166979
rs963748	snp	C/T	0.367708	0.220556	intron-variant	CDC20B	GRCh38.p7	5:55146134	TGAGTCCCTACATCT[C/T]AAACTGCAACCTAAC	166979
rs1021580	snp	C/T	0.305591	0.243741	missense	CDC20B	GRCh38.p7	5:55143638	TTTCTTGTAGGATCC[C/T]GCAAAGAACAACTGA	166979
rs1047689	snp	A/G	0.000155552	0.0088177	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55164231	TGAGAATGCCATTGC[A/G]TTTCTAATAGAACAG	166979
rs1335673	snp	A/G	0.315273	0.241329	intron-variant	CDC20B	GRCh38.p7	5:55150222	TTTAAAAATGGTAAC[A/G]TAGGATAATAGTGAA	166979
rs1393163	snp	A/C	0	0	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55136777	TTGGGAGCCAGAATT[A/C]TGTGTGAGAATCCTC	166979
rs1414365	snp	G/T	0.0558544	0.157504	intron-variant	CDC20B	GRCh38.p7	5:55126642	TTAAAAAGAAGCAGT[G/T]AAACTAAATCACTAG	166979
rs1414366	snp	C/T	0.0372196	0.131242	intron-variant	CDC20B	GRCh38.p7	5:55126885	TGAATTGGAAATGTG[C/T]CCCAGAGAGCTTAAC	166979
rs1501829	snp	C/T	0.0103295	0.0711199	intron-variant	CDC20B	GRCh38.p7	5:55146296	taggaattggaagtg[C/T]gtaggagccggcctg	166979
rs1692473	snp	G/T			intron-variant	CDC20B	GRCh38.p7	5:55126427	taggctggagttcag[G/T]ggcgtgatctcagct	166979
rs1692474	snp	C/T	0.332337	0.236052	intron-variant	CDC20B	GRCh38.p7	5:55126185	ATGTATTTAAGTAAT[C/T]TGATGTAAACTTGAG	166979
rs1697945	snp	A/C	0.297382	0.245469	intron-variant	CDC20B	GRCh38.p7	5:55125597	AGACATTATCCACTG[A/C]TTAGGAATCATATTG	166979
rs2062703	snp	C/T	0	0	intron-variant	CDC20B	GRCh38.p7	5:55142529	TAAGACTTCCTTTTC[C/T]TTCCTCTTATCCTTT	166979
rs2270910	snp	C/G	0.234401	0.249513	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55160906	ATCCTAAACAATTTG[C/G]GGGGGACTATAACCT	166979
rs2407932	snp	A/G	0.300673	0.244811	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55164768	AATCCTTATATATGT[A/G]TGCTTGTTTTGTGTA	166979
rs2645032	snp	C/T	0.0197687	0.0974348	intron-variant	CDC20B	GRCh38.p7	5:55122078	CTTAATTAGTGGGAG[C/T]AGAAGTGTGGAGCAT	166979
rs2783480	snp	C/T	0.0368353	0.130617	intron-variant	CDC20B	GRCh38.p7	5:55132886	CTTTCCAAGTTCTAA[C/T]GATCTTCCAAGACCC	166979
rs2783487	snp	C/T	0.490007	0.0699769	intron-variant	CDC20B	GRCh38.p7	5:55121565	TGCTCTCATAAAGTA[C/T]ATTGTAATGAATACA	166979
rs2935260	snp	A/T	0.363776	0.222609	intron-variant	CDC20B	GRCh38.p7	5:55149052	TCTCCACTGGTAAAC[A/T]CTTAGTCTCTGTCTC	166979
rs2937583	snp	C/T	0.366885	0.220993	intron-variant	CDC20B	GRCh38.p7	5:55148793	aaaaccctgtacata[C/T]ggtttcatacatagt	166979
rs2937584	snp	A/G	0.0414363	0.137845	intron-variant	CDC20B	GRCh38.p7	5:55142898	TTTGAAGGAATCCAT[A/G]TTTCAGTTCGAAAGC	166979
rs2937585	snp	A/G	0.0376037	0.131863	intron-variant	CDC20B	GRCh38.p7	5:55121402	TAATCAGGATATAAC[A/G]ACACGATGGAATATT	166979
rs2992406	snp	A/G	0.363359	0.222822	intron-variant	CDC20B	GRCh38.p7	5:55149155	ggaaatgtaaactaa[A/G]ccacaccaaagcacc	166979
rs3068520	in-del	-/A	0	0	intron-variant	CDC20B	GRCh38.p7	5:55144011	AAAAAAAAAAAAAAA[-/A]CCAGATTTGCACATT	166979
rs3104230	snp	G/T	0.0325213	0.123301	missense	CDC20B	GRCh38.p7	5:55114292	AGAGTGCTGCACCTG[G/T]CTTTGAGTCCAGACC	166979
rs3104237	snp	A/G	0.380138	0.213458	intron-variant	CDC20B	GRCh38.p7	5:55145323	TCTGCAGATTGAAAG[A/G]GAGCCCAGATTTTTT	166979
rs3105152	snp	C/G	0.0387552	0.1337	intron-variant, downstream-variant-500B	CDC20B	GRCh38.p7	5:55136426	GATTACAGGCCTGTG[C/G]TACCACACCTGGCCA	166979
rs3105153	snp	A/G	0.0376037	0.131863	intron-variant	CDC20B	GRCh38.p7	5:55115410	TGAGAAGTACTGCCT[A/G]TTGTTGCCTCATCTC	166979
rs3111178	snp	C/T	0.0414363	0.137845	intron-variant	CDC20B	GRCh38.p7	5:55152436	aatcggagggagtgt[C/T]tattttagtttcatc	166979
rs3111179	snp	C/T	0.467946	0.122472	intron-variant	CDC20B	GRCh38.p7	5:55153129	CTATAGTCCCAGCTG[C/T]TCAGGAGACTGAGGT	166979
rs3111197	snp	C/G	0.0372196	0.131242	intron-variant	CDC20B	GRCh38.p7	5:55132159	ACATTTTTTGAAAAT[C/G]CATCCTTCTTAGTTG	166979
rs3111198	snp	A/T	0.152778	0.230321	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55136576	AAAAAAAAAAAAAAA[A/T]TAGGACAAGCCATAA	166979
rs3111199	snp	C/G	0.0387552	0.1337	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137339	TTTCCTACCAGCTTT[C/G]GGCAAAGAGGTACAC	166979
rs3747725	snp	A/G	0.215144	0.247558	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55166162	TGCATTCACGTTAGG[A/G]GCATGAGCAGAACTG	166979
rs4547887	snp	C/T	0.00159617	0.0282053	intron-variant, splice-acceptor-variant	CDC20B	GRCh38.p7	5:55137637	TGCCACTAAAGTGAT[C/T]TATGGGAAGGGGAGA	166979
rs5867963	in-del	-/G			intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137493	AATTACTTGGCTTAT[-/G]GTGGGATCTGTTTCA	166979
rs5867965	in-del	-/TCTCTT	0.245916	0.249967	intron-variant	CDC20B	GRCh38.p7	5:55145769	TCTCCTCCTCTCTTC[-/TCTCTT]TCTCTTTGTCTCTCT	166979

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