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
rs2019	snp	A/G	0.0637235	0.166737	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	BTRC	GRCh38.p7	10:101557061	TGGAGTGCACTGGCC[A/G]TCCCTCAGATTTGTC	8945
rs14249	snp	A/T	0	0	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	BTRC	GRCh38.p7	10:101556922	GTTAGGAGGGGAGGT[A/T]ACACTTTAAAATACG	8945
rs16405	in-del	-/TCCACTGTT	0.495521	0.0471118	utr-variant-3-prime, cds-indel, nc-transcript-variant	BTRC	GRCh38.p7	10:101553963	TATCATGTCTGAGAA[-/TCCACTGTT]GCCACAGGGTCACTT	8945
rs720356	snp	A/G	0	0	intron-variant	BTRC	GRCh38.p7	10:101386524	AGTACACTTTGGCCA[A/G]AAAACCTGGTTTGGA	8945
rs720357	snp	A/G	0	0	intron-variant	BTRC	GRCh38.p7	10:101386571	CCCACATGCTACTTA[A/G]AAAAAGAGTTTTTAT	8945
rs959754	snp	C/T	0.00597247	0.0543191	intron-variant	BTRC	GRCh38.p7	10:101379688	GCACTCGTTTTTTTA[C/T]GGCCTGTTACAGTCT	8945
rs1045232	snp	C/T	0.385932	0.209815	utr-variant-3-prime, nc-transcript-variant	BTRC	GRCh38.p7	10:101556044	CATTTGTACATGTCC[C/T]TTGGCAAAATTCTTT	8945
rs1045316	snp	A/T			utr-variant-3-prime, nc-transcript-variant	BTRC	GRCh38.p7	10:101553366	AAGATGTCTTCTATC[A/T]TTTGTGAATGATTGG	8945
rs1045324	snp	A/G	0.383439	0.21141	utr-variant-3-prime, nc-transcript-variant	BTRC	GRCh38.p7	10:101553863	GAGTGTCCTCCTCTC[A/G]CATGAGCCAGATCAG	8945
rs2270439	snp	A/C/G/T	0.00842043	0.0643732	missense, nc-transcript-variant	BTRC	GRCh38.p7	10:101550817	CTGCCCAAGCTGAAC[A/C/G/T]CCCCCGTTCCCCTTC	8945
rs3051299	snp	C/T	0.479583	0.0989539	intron-variant	BTRC	GRCh38.p7	10:101385618	TTCTTTCTTCTTCTT[C/T]TTTTTTTTTTTTTTT	8945
rs3095797	snp	G/T	0.381308	0.21274	intron-variant	BTRC	GRCh38.p7	10:101540015	tgcatttgtaactta[G/T]aatatataaaagaat	8945
rs3095798	snp	A/G	0.383439	0.21141	intron-variant	BTRC	GRCh38.p7	10:101539510	TATTGATATACATCA[A/G]CAACATGTAGTGCCA	8945
rs3095799	snp	C/T	0.383632	0.211288	intron-variant	BTRC	GRCh38.p7	10:101538819	CTCAGGTGATCCATC[C/T]GCCTTGACCTCCCAA	8945
rs3095800	snp	A/G	0.381113	0.21286	intron-variant	BTRC	GRCh38.p7	10:101537050	ATAAAAAACCCAAGA[A/G]ATCAAAATTCAAGAT	8945
rs3127231	snp	A/C	0.32885	0.23724	intron-variant	BTRC	GRCh38.p7	10:101541777	attgctggtataaac[A/C]ccacttgttcatgag	8945
rs3127232	snp	A/C	0.197703	0.244469	intron-variant	BTRC	GRCh38.p7	10:101543123	cctcaggtgatccac[A/C]cacctcggcctccca	8945
rs3127233	snp	G/T	0.383439	0.21141	intron-variant	BTRC	GRCh38.p7	10:101543910	accatcttttaagat[G/T]tttttgtttgtttgt	8945
rs3127234	snp	A/G	0.381697	0.212499	intron-variant	BTRC	GRCh38.p7	10:101544355	actttaacatttcat[A/G]tatgcaggtacactg	8945
rs3127235	snp	C/T	0.405082	0.196086	intron-variant	BTRC	GRCh38.p7	10:101544802	ggtgtctcacacctg[C/T]aatcccagcactttg	8945
rs3127236	snp	C/G	0.00636936	0.0560724	intron-variant	BTRC	GRCh38.p7	10:101545088	ctagattgacagtgt[C/G]tttcagcactttaat	8945
rs3127237	snp	C/G	0.0023933	0.0345097	intron-variant	BTRC	GRCh38.p7	10:101546042	ggagacttcagcacc[C/G]cctatcagtaatgga	8945
rs3127238	snp	G/T	0.383632	0.211288	intron-variant	BTRC	GRCh38.p7	10:101546819	caaagaagacaTAAT[G/T]TACTAATATCAGAAA	8945
rs3127239	snp	C/T	0.204189	0.245767	intron-variant	BTRC	GRCh38.p7	10:101551756	GGGCTGTCCTCAGCT[C/T]CTCTTTCTCTCACAG	8945
rs3127240	snp	C/T	0.00636936	0.0560724	intron-variant	BTRC	GRCh38.p7	10:101552322	gcctcctgagtaccg[C/T]gggcacacaacacca	8945
rs3127241	snp	C/G	0.383439	0.21141	intron-variant	BTRC	GRCh38.p7	10:101553091	AGTGAATGTTCTTTT[C/G]TCTTCAAGCAAGTAA	8945
rs3127242	snp	C/T	0.383632	0.211288	utr-variant-3-prime, nc-transcript-variant	BTRC	GRCh38.p7	10:101553842	TGAGAAGAAAGTGTA[C/T]GAAGAGAGTGTCCTC	8945
rs3127243	snp	A/G	0.5	0	intron-variant	BTRC	GRCh38.p7	10:101532784	TGTGTGTGTGTGTGT[A/G]TGTGTGCGCGTGTGC	8945
rs3127244	snp	A/G	0.382085	0.212258	downstream-variant-500B	BTRC	GRCh38.p7	10:101557695	GCAATTTCCAGAGGG[A/G]CTCCAACAAGCTGTA	8945
rs3213772	snp	C/T	0	0	intron-variant	BTRC	GRCh38.p7	10:101533127	CTCTGCTCTGTTCTT[C/T]GTCATAGATAGTAAT	8945
rs3830978	in-del	-/TAT			intron-variant	BTRC	GRCh38.p7	10:101364137	TGGTAAGATGCTTAT[-/TAT]GACAACTATTGTGCT	8945
rs3923214	snp	A/G			intron-variant	BTRC	GRCh38.p7	10:101474296	GGTTTTGTATTTGTT[A/G]AGGTCAGGTGTATTT	8945
rs4130785	snp	A/G	0.381308	0.21274	intron-variant	BTRC	GRCh38.p7	10:101474636	gtggctggcaataga[A/G]aacagaaatcccaga	8945
rs4151059	snp	C/T	0.00144861	0.0268739	synonymous-codon, nc-transcript-variant	BTRC	GRCh38.p7	10:101534722	CATTGTGAAGCAGTT[C/T]TGCACTTGCGTTTCA	8945
rs4151060	snp	G/T	0.055559	0.157139	missense, nc-transcript-variant	BTRC	GRCh38.p7	10:101538342	GACCCCCGTGCTCCT[G/T]CAGGGACACTCTGTC	8945
rs4244343	snp	G/T	0.0652144	0.168387	intron-variant	BTRC	GRCh38.p7	10:101449757	TTCATTTTGCCTTGC[G/T]TATTTCTCTACTTTG	8945
rs4244344	snp	G/T	0.0930568	0.194599	intron-variant	BTRC	GRCh38.p7	10:101461365	TGAACTCATTTTCAG[G/T]TGGATTGTTGTTTTT	8945
rs4244345	snp	C/T	0.424503	0.179021	intron-variant	BTRC	GRCh38.p7	10:101500453	TGGCCCTAATGGAGA[C/T]CAGTTGGTGTATATA	8945
rs4244346	snp	A/G	0.364193	0.222396	intron-variant	BTRC	GRCh38.p7	10:101551871	TGAGTAACGTGAGGG[A/G]CAGCACTCACCTCAC	8945
rs4297403	snp	C/T	0.362313	0.223351	intron-variant	BTRC	GRCh38.p7	10:101469767	CCTTTCTACTTATTT[C/T]CTGCACCACCAATGG	8945
rs4301726	snp	A/T	0.421526	0.181876	intron-variant	BTRC	GRCh38.p7	10:101478867	tcgcttgaaccccgg[A/T]ggcggaggttgcagt	8945
rs4326718	snp	A/G	0.383824	0.211166	intron-variant	BTRC	GRCh38.p7	10:101476001	tactggagaatcttg[A/G]cagacatgtccttag	8945
rs4382828	snp	C/T			intron-variant	BTRC	GRCh38.p7	10:101469750	ggaatgtctcttgtt[C/T]tcctttctacttatt	8945
rs4387286	snp	A/G	0.0865458	0.189163	intron-variant	BTRC	GRCh38.p7	10:101461036	GACTCTCGAGTAGCT[A/G]GGATTACAGGCACCC	8945
rs4421690	snp	C/T	0.00597247	0.0543191	intron-variant	BTRC	GRCh38.p7	10:101387763	ggcgcgatctctgct[C/T]actgcaaactctgcc	8945
rs4429005	snp	C/T	0.081446	0.184634	intron-variant	BTRC	GRCh38.p7	10:101494610	TCTCATTTTCCCTCC[C/T]TGATTCAAGGAACTT	8945
rs4431957	snp	C/T	0.381503	0.21262	intron-variant	BTRC	GRCh38.p7	10:101460925	GTTGTTGTTTTGAGA[C/T]GGAACCTTGCTCTGT	8945
rs4436485	snp	C/G	0.329084	0.237162	intron-variant	BTRC	GRCh38.p7	10:101485604	AACTACCGTGTTTCT[C/G]TAAATTTCTTCAGTG	8945
rs4451650	snp	A/G	0.397813	0.201621	intron-variant	BTRC	GRCh38.p7	10:101445515	GACATAGTGATTGGA[A/G]ACAGTTCACTTCACC	8945
rs4485040	snp	C/T	0.0652144	0.168387	intron-variant	BTRC	GRCh38.p7	10:101451247	CTTCCTCTTTAAGAG[C/T]ACTTCTCCTTTTAAT	8945
rs4485041	snp	C/T	0.200801	0.245111	intron-variant	BTRC	GRCh38.p7	10:101464587	CTAATATCTGTCATT[C/T]AGTGTTGAGATCCAA	8945
rs4612729	snp	C/T	0.497855	0.0326773	intron-variant	BTRC	GRCh38.p7	10:101438885	TGACCAAAATCTCTT[C/T]TGTATTCCCTACTCT	8945
rs4615960	snp	A/G	0.363359	0.222822	intron-variant	BTRC	GRCh38.p7	10:101438198	TTGGGAGGCCAAGGA[A/G]GGCAGATCACAAAGT	8945
rs4639864	snp	C/G	0	0	intron-variant	BTRC	GRCh38.p7	10:101470290	tttgatgagaagttt[C/G]taatagttggatgaa	8945
rs4917939	snp	A/G	0.366679	0.221102	intron-variant	BTRC	GRCh38.p7	10:101387402	ATTCTACAGTGCTGT[A/G]GAACACTAGGACTTA	8945
rs4917940	snp	C/T	0.359998	0.2245	intron-variant	BTRC	GRCh38.p7	10:101427425	CCAGCCTGTGTACAG[C/T]ATTTCTTATAACAAT	8945
rs4917941	snp	C/T	0.0023933	0.0345097	intron-variant	BTRC	GRCh38.p7	10:101518916	agcaagttaaaacaa[C/T]acgtatttattaatt	8945
rs4919541	snp	A/G	0.368938	0.219895	intron-variant	BTRC	GRCh38.p7	10:101394301	TTAGATCTAATTGCC[A/G]ATGACTAATATAATG	8945
rs4919542	snp	G/T	0.0652144	0.168387	intron-variant	BTRC	GRCh38.p7	10:101410115	tgttttaattgtaac[G/T]TCAAAAGCTTTTGAG	8945
rs4919544	snp	A/G	0.365024	0.221967	intron-variant	BTRC	GRCh38.p7	10:101431238	CGCGCCACCACGCCT[A/G]GCTAATTTTTGTATT	8945
rs4919545	snp	A/G	0.366679	0.221102	intron-variant	BTRC	GRCh38.p7	10:101431367	CAGGCAAGAACCACC[A/G]CACACAGACCCCTCA	8945
rs4919546	snp	G/T	0.497416	0.0358495	intron-variant	BTRC	GRCh38.p7	10:101442118	ATGACATAATGTAGC[G/T]GCATATCAGAGTGGC	8945
rs4919547	snp	C/G			intron-variant	BTRC	GRCh38.p7	10:101442282	TCTCTCTCTCTCTCT[C/G]TGTCTCTGTGTGTAT	8945
rs4919548	snp	A/C	0.497359	0.0362457	intron-variant	BTRC	GRCh38.p7	10:101449568	AAAAAATCTGTCCAA[A/C]ACACATAATCGTGAA	8945
rs4919549	snp	A/G	0.497151	0.037632	intron-variant	BTRC	GRCh38.p7	10:101460668	AGAATGACACAGTAC[A/G]TTTTTTATCTCTCAG	8945
rs4919550	snp	C/T	0.0821764	0.185298	intron-variant	BTRC	GRCh38.p7	10:101513021	TAACCATTATATCTC[C/T]CATACACTCTAATAT	8945
rs4919551	snp	C/G	0.332799	0.23589	utr-variant-3-prime, nc-transcript-variant	BTRC	GRCh38.p7	10:101553789	TTCCCATCTACTCCC[C/G]TACGCCCCTTCAACC	8945
rs4919552	snp	A/G	0.495368	0.0478996	utr-variant-3-prime, nc-transcript-variant	BTRC	GRCh38.p7	10:101555421	AAAGGAGATCGGGGC[A/G]ACCCCTGCAGATGTG	8945
rs5025835	snp	A/T			intron-variant	BTRC	GRCh38.p7	10:101505113	CACCTGAGTATATAT[A/T]TATATATATATATGT	8945
rs5787430	in-del	-/T	0.396364	0.202676	intron-variant	BTRC	GRCh38.p7	10:101417010	AAATTGTTTTTTTTT[-/T]CATAAACCACTTGAG	8945
rs5787432	in-del	-/AGG	0.00597247	0.0543191	intron-variant	BTRC	GRCh38.p7	10:101462114	AGCAAAACAAAAGAC[-/AGG]AGGAAACCCTTGATT	8945
rs5787433	in-del	-/TTC	0.00716266	0.059414	intron-variant	BTRC	GRCh38.p7	10:101469476	GTTATTACATATTCA[-/TTC]ATGAAGGGAAAAGAG	8945
rs5787434	in-del	-/G			intron-variant	BTRC	GRCh38.p7	10:101469633	AAGTTTTCATACAGT[-/G]GAATTTTACAGATAT	8945
rs5787436	in-del	-/TCTC			intron-variant	BTRC	GRCh38.p7	10:101527788	CTCTCTCTCTCTCTC[-/TCTC]ACATACACACACACA	8945
rs5787437	in-del	-/AC			intron-variant	BTRC	GRCh38.p7	10:101527796	CTCTCTCTCTCACAT[-/AC]ACACACACACACACA	8945
rs5787439	in-del	-/GC/GCGC	0.345835	0.231793	intron-variant	BTRC	GRCh38.p7	10:101532797	TGTGTGTGCGCGTGT[-/GC/GCGC]GCGCGCGCGCGCGCT	8945
rs6421336	snp	G/T			intron-variant	BTRC	GRCh38.p7	10:101415491	tttattttattttat[G/T]ttatgttatgttatg	8945
rs6584422	snp	C/T	0.402454	0.198136	intron-variant	BTRC	GRCh38.p7	10:101402573	GAAAATAATTCCTAT[C/T]TTAAAAATTCTATAT	8945
rs6584423	snp	A/G	0.497881	0.0324789	intron-variant	BTRC	GRCh38.p7	10:101431316	TCCTGACCTCAGGTA[A/G]TCCACCCATCTCGGC	8945
rs6584424	snp	A/G	0.495927	0.0449436	intron-variant	BTRC	GRCh38.p7	10:101489279	TTCCCAGAATCAAGA[A/G]TAAAAGCAACCCAGA	8945
rs6584427	snp	G/T	0.0023933	0.0345097	intron-variant	BTRC	GRCh38.p7	10:101509085	GGGCGCTAGCCCTTC[G/T]GGGTTCCTTTTCTTT	8945
rs6584428	snp	A/G	0.0818113	0.184966	intron-variant, upstream-variant-2KB	BTRC	GRCh38.p7	10:101514483	ttttttttttgagaa[A/G]gctctgtcacccaat	8945
rs6584429	snp	C/G	0.388555	0.208093	intron-variant	BTRC	GRCh38.p7	10:101521877	CTCTGCCAGGTATGT[C/G]TACAAGTGTTTGTAA	8945
rs6584430	snp	A/G	0.414173	0.18854	intron-variant	BTRC	GRCh38.p7	10:101521919	GCTATGATGATAAGA[A/G]AACTAGATCTCCAGC	8945
rs7072719	snp	A/T	0.376592	0.215579	intron-variant	BTRC	GRCh38.p7	10:101385743	CAGACACACACACAC[A/T]CATATGTTTTGTACA	8945
rs7073902	snp	A/C	0.0869089	0.189476	intron-variant	BTRC	GRCh38.p7	10:101532136	GAAGAATATTTTATA[A/C]ATATAGATAGTAGCC	8945
rs7074011	snp	A/G	0.0788843	0.182262	intron-variant	BTRC	GRCh38.p7	10:101386613	AAAAAGTATTGTGGA[A/G]Tacttcttcttttta	8945
rs7079033	snp	C/G	0.0217236	0.101931	intron-variant	BTRC	GRCh38.p7	10:101415165	gtgccctatataggt[C/G]taccattttttatct	8945
rs7082055	snp	A/G	0.319856	0.240042	intron-variant	BTRC	GRCh38.p7	10:101428164	GGATGACAGGGAGAA[A/G]GAAATTATAAGTTTA	8945
rs7082104	snp	C/G	0.497182	0.037434	intron-variant	BTRC	GRCh38.p7	10:101458435	ggcggtgttatacaa[C/G]tgtatgtttttgtca	8945
rs7082129	snp	A/G	0.381113	0.21286	intron-variant	BTRC	GRCh38.p7	10:101428444	GGTGAGGAAACGTTG[A/G]AAACAGTGAACAAAG	8945
rs7084859	snp	C/T	0.031825	0.122064	intron-variant	BTRC	GRCh38.p7	10:101551884	GGGCAGCACTCACCT[C/T]ACGGAACCCTGTGAA	8945
rs7085932	snp	A/C	0.497329	0.0364438	intron-variant	BTRC	GRCh38.p7	10:101401051	GTAGTGTAGTTATTT[A/C]AAATAATATTTAATA	8945
rs7087443	snp	C/T	0.0023933	0.0345097	intron-variant	BTRC	GRCh38.p7	10:101508400	GTTCACTAATCAGAT[C/T]TGACATGTTTATGAG	8945
rs7088165	snp	A/G	0.00666659	0.0573485	missense, nc-transcript-variant	BTRC	GRCh38.p7	10:101534782	GATCGTTCCATTGCT[A/G]TATGGGATATGGCCT	8945
rs7088533	snp	A/G			intron-variant	BTRC	GRCh38.p7	10:101505143	tgtatatatatgtat[A/G]tatatatgtatatgt	8945
rs7088547	snp	A/G			intron-variant	BTRC	GRCh38.p7	10:101505149	tatatgtatatatat[A/G]tgtatatgtatatat	8945
rs7088890	snp	A/G			intron-variant	BTRC	GRCh38.p7	10:101505139	tatgtgtatatatat[A/G]tatatatatatgtat	8945
rs7088899	snp	A/G			intron-variant	BTRC	GRCh38.p7	10:101505157	tatatatatgtatat[A/G]tatatatatatatat	8945
rs7090670	snp	A/C	0.497613	0.0344622	intron-variant	BTRC	GRCh38.p7	10:101364700	TACACCAAACTGTTA[A/C]TGTGGTTATTTGTGA	8945

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