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
rs7189	snp	C/T	0.142609	0.225759	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	MRPL12, HGS	GRCh38.p7	17:81701867	CTCCCAGGGGAAGCC[C/T]CCAGCCCTGTGGGTC	9146
rs1128805	snp	C/T	0.185184	0.241452	upstream-variant-2KB, utr-variant-3-prime	MRPL12, HGS	GRCh38.p7	17:81701634	CCCAGGCCATGCTCA[C/T]GTCCGGAGTAACACT	9146
rs1139303	snp	A/G			upstream-variant-2KB, downstream-variant-500B	MRPL12, HGS	GRCh38.p7	17:81702235	gggaggctgaggccc[A/G]agaatcgcttgaacc	9146
rs3088017	snp	A/G	0.0582	0.160352	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	MRPL12, HGS	GRCh38.p7	17:81701969	CCAGGCCACACCCAG[A/G]CACCACAGCCAGCTC	9146
rs3205137	snp	C/T	0.375598	0.21616	intron-variant, utr-variant-5-prime, upstream-variant-2KB	ARL16, HGS	GRCh38.p7	17:81682274	ACTCGGAGCGAGACT[C/T]CGTCTCAAAAAATAA	9146
rs4074682	snp	C/T	0.00319258	0.0398258	intron-variant	HGS	GRCh38.p7	17:81690763	TTCCCACCTGGGGGG[C/T]TCTACAGCCCCGGCC	9146
rs6565620	snp	C/T	0.16911	0.236552	intron-variant	HGS	GRCh38.p7	17:81691070	CCATCTGGATTCTTA[C/T]CCTCGAGGCATCTTC	9146
rs6565621	snp	C/T	0.378372	0.214524	intron-variant	HGS	GRCh38.p7	17:81698382	cgcccttctcggcct[C/T]ccaaagtgctgggat	9146
rs7208144	snp	A/G	0.469247	0.120128	intron-variant	HGS	GRCh38.p7	17:81687778	CTCCCCTTCTGTCCC[A/G]ACCTGTGGGCCAGAC	9146
rs7214125	snp	A/G	0.359787	0.224604	intron-variant, upstream-variant-2KB	HGS, MIR6786	GRCh38.p7	17:81692597	TGGCAGGGCATCCCA[A/G]CGCCATTCCTGCCTT	9146
rs7215738	snp	C/T	0.16846	0.236329	intron-variant, upstream-variant-2KB	HGS, MIR6786	GRCh38.p7	17:81692817	gaaatcccgtctcta[C/T]tttttaagtatttta	9146
rs7216239	snp	C/T	0.140242	0.224618	intron-variant, upstream-variant-2KB	HGS, MIR6786	GRCh38.p7	17:81693157	ACTGACCTGTTTGCC[C/T]CTTCTTGGGTGGGGC	9146
rs7218012	snp	A/G	0.000994431	0.0222761	intron-variant	HGS	GRCh38.p7	17:81695079	GGAGGTGAGGGGGCC[A/G]CTCCCGGCATTCCTA	9146
rs7406440	snp	A/G	0.104149	0.203046	intron-variant	HGS	GRCh38.p7	17:81699482	ccaggctggagtgca[A/G]tggtgcgacgtcagc	9146
rs7406945	snp	C/T	0.238749	0.249747	intron-variant	HGS	GRCh38.p7	17:81699478	tcgcccaggctggag[C/T]gcagtggtgcgacgt	9146
rs7503637	snp	A/G	0.193653	0.243567	intron-variant, utr-variant-5-prime, upstream-variant-2KB	ARL16, HGS	GRCh38.p7	17:81682485	CTGACCTCGTGATTC[A/G]CCCACCTCAGCTTCC	9146
rs8066889	snp	G/T	0.340396	0.233095	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ARL16, HGS	GRCh38.p7	17:81683798	GCTCGGCGCCGCGGC[G/T]CAAGGCCCGCCCACC	9146
rs8067764	snp	A/C/G/T	0.00161663	0.0283849	intron-variant, missense	HGS	GRCh38.p7	17:81701244	TACGTCTGCTCACAG[A/C/G/T]GGGAGACGCATACCC	9146
rs8070488	snp	C/T	0.338152	0.233943	synonymous-codon	HGS	GRCh38.p7	17:81696901	CAGCACCTTCAGCCC[C/T]GCCGGCTCGGTGGAG	9146
rs8073335	snp	C/T	0.0023933	0.0345097	intron-variant	HGS	GRCh38.p7	17:81686033	cctcccaagctcaaa[C/T]gatcgtcccacctca	9146
rs8074828	snp	C/G	0.172028	0.23753	intron-variant	HGS	GRCh38.p7	17:81690106	TGCGTTGCAGCTGCC[C/G]AGAGTGAGGAAGGGG	9146
rs8080080	snp	C/T	0.02016	0.0983543	intron-variant	HGS	GRCh38.p7	17:81690541	GCCGCTGGGAAGGGC[C/T]GCCCGGGGCATTGCT	9146
rs8080624	snp	C/G	0.387302	0.208921	intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ARL16, HGS	GRCh38.p7	17:81683645	TGAGTCCCCGCCCCA[C/G]TCCGGGTGCCCCCCG	9146
rs8081820	snp	A/G	0.00119737	0.0244387	intron-variant	HGS	GRCh38.p7	17:81687582	GCTGTTTTGGAGAGC[A/G]AGGGCTTCATGCTTT	9146
rs9890692	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	ARL16, HGS	GRCh38.p7	17:81683980	GCGTGCGCGCACTGG[A/G]GGGAAAAGGCGGAAG	9146
rs11541091	snp	C/T			synonymous-codon, utr-variant-5-prime	HGS	GRCh38.p7	17:81687078	CAGACCATGGAGGAG[C/T]TGAAGGACCTGCTGA	9146
rs11867435	snp	A/G	0.298905	0.24517	intron-variant	HGS	GRCh38.p7	17:81688202	GCGAGGCCAGGCTGC[A/G]CTCTAACCGGGGGAG	9146
rs11867543	snp	C/T	0.165853	0.235413	intron-variant	HGS	GRCh38.p7	17:81688016	TGAGCCGGTTCGCTC[C/T]TCTGGGGTGAGGCAG	9146
rs11870742	snp	A/G	0	0	intron-variant	HGS	GRCh38.p7	17:81698233	gcccgggaagtggag[A/G]ttgcagtgagccgag	9146
rs11871678	snp	A/G	0.138886	0.22395	intron-variant	HGS	GRCh38.p7	17:81687255	TCGCACTCATGAGTC[A/G]GAGAGACAGGGCCGT	9146
rs12450153	snp	A/G	0.284733	0.247575	intron-variant	HGS	GRCh38.p7	17:81688955	AGGGAGGAGGGCGGT[A/G]GCCTGGAGCCAGGGA	9146
rs12451387	snp	A/G	0.280845	0.24809	intron-variant	HGS	GRCh38.p7	17:81690643	CTGGTGGGGCGGGAA[A/G]CGTGTGGTCCTGACT	9146
rs12452113	snp	A/G	0.409212	0.192748	intron-variant	HGS	GRCh38.p7	17:81688221	TAACCGGGGGAGAGG[A/G]TGGCTGCAGGGGGTC	9146
rs12452184	snp	C/T	0.499891	0.00738737	intron-variant	HGS	GRCh38.p7	17:81697396	TTCCCCAGTCAGCTT[C/T]TGTGTTTTGTGACAT	9146
rs12936025	snp	C/T	0.331874	0.236213	intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ARL16, HGS	GRCh38.p7	17:81682531	ACAGGAGTAAGCCAC[C/T]GCGCCCGGCCCAAAG	9146
rs12937833	snp	C/T	0.152001	0.229992	intron-variant, upstream-variant-2KB	HGS, MIR6786	GRCh38.p7	17:81692885	GCTTGGTGGCAGATG[C/T]CTGTAGTCCCAGCTA	9146
rs12937971	snp	C/T			intron-variant	HGS	GRCh38.p7	17:81699594	ccatgcccagctagt[C/T]tttgtatttttatta	9146
rs12946356	snp	C/T	0.164219	0.234823	intron-variant, upstream-variant-2KB	HGS, MIR6786	GRCh38.p7	17:81692829	CTACTTTTTAAGTAT[C/T]TTATACTTAAAATTT	9146
rs12946662	snp	C/T	0.152667	0.230274	intron-variant, upstream-variant-2KB	HGS, MIR6786	GRCh38.p7	17:81692312	CTCCCTGTCTCGCTC[C/T]GTGGACATTTCTGGG	9146
rs12949340	snp	A/G	0.177503	0.239258	intron-variant	HGS	GRCh38.p7	17:81689097	ACAGCCTGTTTCAGA[A/G]TGGCAGGACTCCTGG	9146
rs12951171	snp	C/T	0.134418	0.221677	synonymous-codon	HGS	GRCh38.p7	17:81696850	GCCCGCAGCCGGAGG[C/T]GTGCTCTACCAGCCC	9146
rs12952375	snp	C/T	0.178144	0.239451	intron-variant	HGS	GRCh38.p7	17:81690077	ACACCTTCACTTGGG[C/T]GCACGGTCACTGCTG	9146
rs34033471	snp	C/T	0.153332	0.230554	intron-variant	HGS	GRCh38.p7	17:81691270	TGGCGTTGAGACTCC[C/T]GGGAGCATGTCCAGG	9146
rs34043613	in-del	-/T			intron-variant	HGS	GRCh38.p7	17:81690422	GGTGGAGACGTGGCT[-/T]GAGGGCCTTTAGAGT	9146
rs34159103	in-del	-/T			intron-variant	HGS	GRCh38.p7	17:81690493	AGGAAGGAAGTCCCT[-/T]CCTCAGGCCTCGGCA	9146
rs34203932	snp	A/G	0.178785	0.239642	intron-variant	HGS	GRCh38.p7	17:81690810	GCCGTGCACAAGGCC[A/G]CCGTCCCTGCTGGGC	9146
rs34264473	snp	C/T	0.197082	0.244335	intron-variant	HGS	GRCh38.p7	17:81687527	TGGGAGGGCTCTGAG[C/T]GGGGGCTTGTAAGAT	9146
rs34276461	snp	A/G	0.19646	0.2442	intron-variant	HGS	GRCh38.p7	17:81687753	AAGAGTGTCCCATGT[A/G]GTCAGGCTGCTCCCC	9146
rs34340361	snp	G/T	0.011272	0.0742224	synonymous-codon, downstream-variant-500B	HGS, MIR6786	GRCh38.p7	17:81693920	GGAGCCCATGCCCTC[G/T]GCCTCCTCAGCGCCC	9146
rs34384005	snp	A/G	0.13802	0.223518	synonymous-codon	HGS	GRCh38.p7	17:81695037	TGCACAGCCTGGGGA[A/G]GGGCACGCAGCCCCC	9146
rs34467268	in-del	-/G			upstream-variant-2KB, intron-variant	ARL16, HGS	GRCh38.p7	17:81684335	GAGGGTCCGCGCAGG[-/G]CGCCAGGGGCGCTCG	9146
rs34709589	snp	A/G	0.198014	0.244535	upstream-variant-2KB, intron-variant	ARL16, HGS	GRCh38.p7	17:81685135	CACTTGGCTTGGAGC[A/G]AGGGGCCTGGAGTCT	9146
rs34730558	snp	C/T	0.154993	0.231244	upstream-variant-2KB, intron-variant	ARL16, HGS	GRCh38.p7	17:81685457	CCCTGCCCATCAGCA[C/T]GCTCAGGAGGATTCT	9146
rs34764239	in-del	-/T			intron-variant	HGS	GRCh38.p7	17:81698865	CTGAGGTCAGGAGTT[-/T]GGAGACTGGCCTGGC	9146
rs34784238	snp	G/T	0.202035	0.245356	intron-variant	HGS	GRCh38.p7	17:81691382	CGTACGGGGTGGTTC[G/T]GGGCCGGGTGGCGCA	9146
rs34815730	snp	A/G	0.343106	0.232016	intron-variant, upstream-variant-2KB	ARL16, HGS	GRCh38.p7	17:81683151	AAACCACGATGCAAA[A/G]AGAACAATACAACCG	9146
rs34844749	in-del	-/T	0.279195	0.248289	intron-variant	HGS	GRCh38.p7	17:81697618	CTGTTTTGCCCTTTA[-/T]CAGATGTCTCTTGGG	9146
rs34868130	snp	A/C/G	0.00780263	0.0619736	synonymous-codon, missense	HGS	GRCh38.p7	17:81695806	GTTCCACAATGGCGA[A/C/G]TCTGAGGAGAGCCAC	9146
rs34876268	snp	A/G	0.199254	0.244796	intron-variant	HGS	GRCh38.p7	17:81687707	TGTGGACTGTGATGC[A/G]GTGGGGATGCTGTTG	9146
rs34897798	snp	C/T	0.215581	0.247619	upstream-variant-2KB, synonymous-codon, utr-variant-3-prime	MRPL12, HGS	GRCh38.p7	17:81701522	GATGGCACCCTCTGG[C/T]GGTCCCCCCCAGCAG	9146
rs34975185	snp	A/G	0.179105	0.239737	upstream-variant-2KB, intron-variant	ARL16, HGS	GRCh38.p7	17:81685235	GGGACTCCAAGGGAC[A/G]GGTGATAGGGTTCTT	9146
rs35078912	snp	C/T	0.033273	0.124617	synonymous-codon	HGS	GRCh38.p7	17:81694844	TCTGGCTGAGGACAT[C/T]GACCCTGAGGTAAGG	9146
rs35108781	snp	C/T	0.00358184	0.0421674	synonymous-codon	HGS	GRCh38.p7	17:81695980	GCTGGAGCTGCTCAA[C/T]CAGCTGGACGAGCGC	9146
rs35172594	snp	A/C			intron-variant	HGS	GRCh38.p7	17:81699066	AGCGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA	9146
rs35477855	in-del	-/G			intron-variant	HGS	GRCh38.p7	17:81690572	CTCGCTCGTGCTGGG[-/G]TCCTCTCTGGGTCCG	9146
rs35569308	snp	A/G	0.179744	0.239925	upstream-variant-2KB, intron-variant	ARL16, HGS	GRCh38.p7	17:81685119	GCCCTTATTTCCAAA[A/G]CACTTGGCTTGGAGC	9146
rs35618583	snp	A/G	0.177824	0.239355	intron-variant	HGS	GRCh38.p7	17:81691219	TTTTTCCTTGCCCTT[A/G]CTTTTAACTTACCTT	9146
rs35646762	snp	C/T	0.163892	0.234703	intron-variant	HGS	GRCh38.p7	17:81695719	CTGGGTGCCTCCATC[C/T]CAGGCCCCACCAGGG	9146
rs35821128	snp	A/G	0.24449	0.249939	upstream-variant-2KB, intron-variant	ARL16, HGS	GRCh38.p7	17:81684344	CGCAGGGCGCCAGGG[A/G]CGCTCGGCGACCTCG	9146
rs35976578	in-del	-/C			intron-variant	HGS	GRCh38.p7	17:81699065	AGCGAGACTCCGTCT[-/C]CAAAAAAAAAAAAAA	9146
rs36074783	snp	C/T	0.186421	0.24178	intron-variant	HGS	GRCh38.p7	17:81695451	TCTGTGGACCTAACA[C/T]GGACCTGAATATTCC	9146
rs55837949	snp	A/G	0.39047	0.206821	intron-variant	HGS	GRCh38.p7	17:81701196	CTTCACGGTTTAGCA[A/G]TGGGACCCCTGGCCC	9146
rs55842573	snp	C/T	0.139564	0.224285	intron-variant	HGS	GRCh38.p7	17:81697553	CCGTCAGTCCCATTG[C/T]TGGCCGTTCGGCTGA	9146
rs56058441	snp	G/T	0.133334	0.221109	missense	HGS	GRCh38.p7	17:81701105	CAGCAGCCCTACATC[G/T]CGGGGCAGCAGCCCA	9146
rs56141149	snp	G/T	0.186421	0.24178	intron-variant	HGS	GRCh38.p7	17:81697413	GTGTTTTGTGACATC[G/T]ACTGTCCCAAGAGCA	9146
rs56210089	snp	A/C/G	7.36241e-05	0.00606685	intron-variant	HGS	GRCh38.p7	17:81701232	GGGATTGTCCCGTAC[A/C/G]TCTGCTCACAGGGGG	9146
rs56267991	snp	C/T	0.0655868	0.168795	intron-variant	HGS	GRCh38.p7	17:81689719	GCAGGGGGCGCTGCA[C/T]GAGCTGCCTTGGACC	9146
rs57366978	snp	A/G	0.287085	0.247234	intron-variant	HGS	GRCh38.p7	17:81691250	ATTTTCCCCAAAACG[A/G]TGGCTGGCGTTGAGA	9146
rs58038388	snp	C/T	0.0452528	0.143452	intron-variant	HGS	GRCh38.p7	17:81688371	ACACCACGCTGCCAC[C/T]GTCAGGCCTGCCGGG	9146
rs58150169	snp	C/T	0.0821764	0.185298	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	MRPL12, HGS	GRCh38.p7	17:81701782	CTCCCTTGTCCTCAG[C/T]CTACTGCAGTCCCTG	9146
rs58168109	snp	G/T	0.0228589	0.104436	intron-variant	HGS	GRCh38.p7	17:81701140	CCAGCAGGTGAGCCA[G/T]TCCCGGGGCCTCACA	9146
rs58432187	snp	A/C			intron-variant	HGS	GRCh38.p7	17:81688671	GGCGCCTGGAGTGTC[A/C]TGCGACCCTCACCCC	9146
rs58744152	snp	C/G	0.0256215	0.110247	intron-variant	HGS	GRCh38.p7	17:81686575	TCACGCTGAGGGAGA[C/G]ACAGGAGATAGGGGA	9146
rs58903919	in-del	-/TGCCC			intron-variant	HGS	GRCh38.p7	17:81696203	TGCCCTGCCCTGCCC[-/TGCCC]AGGACCCTCTGCCTG	9146
rs59387473	in-del	-/C	0	0	intron-variant	HGS	GRCh38.p7	17:81697363	TGCCCCCCCCCCCCC[-/C]GCCTTTAATCTAGAG	9146
rs59761257	in-del	-/TGCCCTGCCC			intron-variant	HGS	GRCh38.p7	17:81696194	TGCCCTGCCCTGCCC[-/TGCCCTGCCC]AGGACCCTCTGCCTG	9146
rs60761605	snp	C/T	0.0256215	0.110247	intron-variant	HGS	GRCh38.p7	17:81686236	GCACCTGGCAGCAGA[C/T]GAGCTTTTCTCATCT	9146
rs61156089	snp	A/C/T	0.000456425	0.0150998	intron-variant	HGS	GRCh38.p7	17:81688661	CGAGGCCTCTGGCGC[A/C/T]TGGAGTGTCCTGCGA	9146
rs62077175	snp	G/T	0.172674	0.237741	intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ARL16, HGS	GRCh38.p7	17:81682538	TAAGCCACCGCGCCC[G/T]GCCCAAAGTAGCTTT	9146
rs62077177	snp	A/G	0.0452528	0.143452	intron-variant	HGS	GRCh38.p7	17:81687609	CTTTCCTGGGCAGAG[A/G]AGGAAAAGCCCTCCA	9146
rs62077179	snp	C/T	0.0111196	0.0737302	intron-variant	HGS	GRCh38.p7	17:81688989	CCGTGCATGTGAGGG[C/T]GGGTTCAGACCGGCT	9146
rs62077181	snp	G/T	0.0322583	0.122835	intron-variant	HGS	GRCh38.p7	17:81690241	GCCGAGAGAGTGAGT[G/T]TGGGCGGCCGCCAGG	9146
rs62077183	snp	A/C/T	0.172687	0.238702	intron-variant, upstream-variant-2KB	HGS, MIR6786	GRCh38.p7	17:81691910	GAGAAGCTGCGGGGC[A/C/T]GCGGCCAGTGCCTCA	9146
rs62077184	snp	C/T	0.488965	0.0734569	intron-variant	HGS	GRCh38.p7	17:81700245	GTAGTGGCGTACGCC[C/T]GTAATCCCAGCTACT	9146
rs62077185	snp	A/T	0.5	0	intron-variant	HGS	GRCh38.p7	17:81700674	CAGCCCCTTCTCCCA[A/T]GGCACTCATTCCCTC	9146
rs62622513	snp	C/T	0.000827953	0.0203296	intron-variant, upstream-variant-2KB	ARL16, HGS	GRCh38.p7	17:81682943	CTACACACAGCAAGG[C/T]TGGGGACTGGACGTC	9146
rs66508304	snp	A/C	0.178144	0.239451	intron-variant	HGS	GRCh38.p7	17:81686176	GCTCAAGCAATCCTC[A/C]TGCCTTGGCCTCCCA	9146
rs66717663	in-del	-/A	0	0	intron-variant	HGS	GRCh38.p7	17:81699082	AAAAAAAAAAAAAAA[-/A]TCCATGAGTTAATTC	9146
rs67606182	snp	C/T	0.202035	0.245356	intron-variant	HGS	GRCh38.p7	17:81687268	TCGGAGAGACAGGGC[C/T]GTGAGCCCCAATCCA	9146
rs67703038	snp	C/T	0.153332	0.230554	intron-variant	HGS	GRCh38.p7	17:81686229	AGCCACTGCACCTGG[C/T]AGCAGATGAGCTTTT	9146

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