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
rs179685	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KMT2B	GRCh38.p7	19:35721913	AAAGGCAGGTTCTGA[G/T]GGTTCCCCGCAATGC	9757
rs179686	snp	A/G	0.00190231	0.0307821	missense, upstream-variant-2KB, nc-transcript-variant	KMT2B	GRCh38.p7	19:35721608	TGTGGCTGTGGTGGC[A/G]GTAGTGCCTGGGGCA	9757
rs231590	snp	C/G	0	0	intron-variant	KMT2B	GRCh38.p7	19:35734380	GGCACAGGGTGGGGC[C/G]TTGTGTCCAAGTCCA	9757
rs231591	snp	C/T	0.497804	0.0330613	missense	KMT2B	GRCh38.p7	19:35733804	ACCTGGGGAGGACCA[C/T]CTTCCGGAAGTGGCA	9757
rs231592	snp	C/T	0.471388	0.116136	intron-variant	KMT2B	GRCh38.p7	19:35728308	CCAGGGAATCTCACC[C/T]GGGTTCCACCACCCT	9757
rs231593	snp	C/T	0.00597247	0.0543191	intron-variant	KMT2B	GRCh38.p7	19:35726873	cctcagcctcccgag[C/T]agctgagattacagg	9757
rs231594	snp	C/T	0.00189947	0.0307591	intron-variant	KMT2B	GRCh38.p7	19:35723286	GAATGAGGTCACGCC[C/T]CAGCTACTCACACAC	9757
rs231595	snp	A/G	0.0063344	0.0559203	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	KMT2B	GRCh38.p7	19:35723272	CCCAGCTACTCACAC[A/G]CAGCACTGCTTCTTG	9757
rs1051909	snp	C/T	0.0376037	0.131863	downstream-variant-500B, utr-variant-3-prime, intron-variant	IGFLR1, KMT2B	GRCh38.p7	19:35738738	AGCCCATCCAGCAAT[C/T]GCCCCCTTTCTGCCC	9757
rs1052491	snp	A/G	0.180913	0.240265	synonymous-codon, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	ZBTB32, KMT2B	GRCh38.p7	19:35716608	CGGCTGTCCCAGCCT[A/G]GCCTCCATGCAGGCG	9757
rs1131995	snp	A/C			utr-variant-3-prime, nc-transcript-variant	IGFLR1, KMT2B	GRCh38.p7	19:35738854	GGTGGGAACCCCCCC[A/C]CAATAAAGTCTGTCA	9757
rs1268319	snp	A/G	0.0221141	0.102801	intron-variant	KMT2B	GRCh38.p7	19:35736329	ATTTAAAATACTGGA[A/G]AATTGTATTTTGCAC	9757
rs2234371	snp	A/G	0.298323	0.245301	intron-variant, upstream-variant-2KB, nc-transcript-variant	ZBTB32, KMT2B	GRCh38.p7	19:35716084	TGGTACAGTGAGTTG[A/G]CGCTGGGATTCCTGG	9757
rs2234372	snp	G/T	0	0	synonymous-codon, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	ZBTB32, KMT2B	GRCh38.p7	19:35716140	CCCCACAGGCGCACT[G/T]GCAACCTGTGCGGGT	9757
rs2234373	snp	A/G	0.0201234	0.0982687	missense, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	ZBTB32, KMT2B	GRCh38.p7	19:35716175	AGGACAAGGCAGGCT[A/G]CCCACCTCGCCCGCA	9757
rs2234374	snp	A/G	0.0061701	0.0551995	synonymous-codon, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	ZBTB32, KMT2B	GRCh38.p7	19:35716200	CCCGCACCCTCCCCC[A/G]GCCCCTCCTGCTCGG	9757
rs2234375	snp	C/G	0.20105	0.245166	intron-variant, upstream-variant-2KB, utr-variant-3-prime	ZBTB32, KMT2B	GRCh38.p7	19:35716434	TGGCCAGCTTTCGCC[C/G]CCTTCTTCCTTCCTT	9757
rs2234376	snp	C/T	0.00188754	0.0306628	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	ZBTB32, KMT2B	GRCh38.p7	19:35716802	TTAAAGAACGAAAAG[C/T]GGGCCGGCTCGGCTT	9757
rs2242519	snp	C/G	0.00195722	0.0312215	missense, nc-transcript-variant	KMT2B	GRCh38.p7	19:35721107	CTCCACCACGTGCCC[C/G]AACTCCTCCATCTAC	9757
rs2242520	snp	A/G	0.386966	0.209142	intron-variant	KMT2B	GRCh38.p7	19:35730150	AACTGTGGGGTACAC[A/G]GTTCCTTCCCCACCT	9757
rs2242521	snp	A/G	0.134802	0.221877	intron-variant	KMT2B	GRCh38.p7	19:35731116	CTTTTGGACGACTGC[A/G]GGGAGTAGAGTGCTT	9757
rs2242522	snp	G/T	0.496751	0.0401712	intron-variant	KMT2B	GRCh38.p7	19:35738053	TTCCCTGTTCATCCT[G/T]CCCTGCAGATCAGCC	9757
rs2280743	snp	C/T	0.405429	0.195811	intron-variant	KMT2B	GRCh38.p7	19:35735098	CAGTCCTGCTGTGTT[C/T]GGGAAACTGGAAGTG	9757
rs2293684	snp	A/G	6.64651e-05	0.00576438	intron-variant, downstream-variant-500B	KMT2B	GRCh38.p7	19:35728899	CAGCAGGTACTGGGA[A/G]GTGGGGGTCCAGAAG	9757
rs2293685	snp	C/T			intron-variant	KMT2B	GRCh38.p7	19:35736143	gtaatctcagctact[C/T]gggagactgaggcag	9757
rs3787051	snp	C/T	0.292266	0.246401	intron-variant	KMT2B	GRCh38.p7	19:35727056	TAGCTGCCTCCACTA[C/T]GCCCCTGTTTTGGGC	9757
rs3848662	snp	G/T	0.229136	0.249128	intron-variant	KMT2B	GRCh38.p7	19:35725155	TGACTGTGTCATCGA[G/T]AAGCCAGGTGGGTCT	9757
rs3848663	snp	A/G	0.294064	0.246086	intron-variant	KMT2B	GRCh38.p7	19:35734719	TGGCGGTGGAGTGGT[A/G]GAGTTTTCTGTTGGT	9757
rs3848664	snp	C/T	0.0829062	0.185956	downstream-variant-500B, utr-variant-3-prime, intron-variant	IGFLR1, KMT2B	GRCh38.p7	19:35738742	CATCCAGCAATCGCC[C/T]CCTTTCTGCCCTGGG	9757
rs3888030	snp	A/C	0.0191108	0.0958655	intron-variant	KMT2B	GRCh38.p7	19:35725367	TTCACAGACCCCCAG[A/C]TCTCTGTCGGTCCTC	9757
rs4358062	snp	G/T	0	0	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	IGFLR1, KMT2B	GRCh38.p7	19:35739024	AGTCATGGGGTCTGT[G/T]ACGGCTTCAGAACAA	9757
rs4806198	snp	C/T	0.294576	0.245994	intron-variant	KMT2B	GRCh38.p7	19:35731122	GACGACTGCAGGGAG[C/T]AGAGTGCTTACAGCT	9757
rs7247731	snp	C/T	0.175254	0.238565	intron-variant	KMT2B	GRCh38.p7	19:35718778	ACCTGTGGGCCGCCC[C/T]GCCGGGCCTCGCAAC	9757
rs7258564	snp	A/T	0	0	intron-variant	KMT2B	GRCh38.p7	19:35734034	GGGGAGCCTCTGGCC[A/T]TGTGGGAGAAACAGA	9757
rs8106959	snp	A/G	0.245061	0.249951	intron-variant	KMT2B	GRCh38.p7	19:35728624	TGTCCAAGCTGGCAC[A/G]AGAGGGCCTGGCTTA	9757
rs10402837	snp	A/G	0.239902	0.249796	intron-variant	KMT2B	GRCh38.p7	19:35726909	gaatcgcttgaaccc[A/G]ggaggcggaggttgc	9757
rs11084828	snp	C/T	0.28807	0.247084	intron-variant, upstream-variant-2KB	KMT2B	GRCh38.p7	19:35722559	CACACACTCCGATTT[C/T]TCCCCCAGGGTCCCG	9757
rs11348412	in-del	-/G	0.0140439	0.0826118	intron-variant	KMT2B	GRCh38.p7	19:35724631	TGCTCATTGTGTCCT[-/G]CCTAGAGCTGCCACT	9757
rs11380823	in-del	-/G	0	0	intron-variant	KMT2B	GRCh38.p7	19:35728500	CGGTGGGGGCCCGGA[-/G]GGGGTACCTGCTGGA	9757
rs11539593	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, intron-variant	IGFLR1, KMT2B	GRCh38.p7	19:35738748	GCAATCGCCCCCTTT[C/T]TGCCCTGGGGGCCCA	9757
rs11670414	snp	C/T	0.26654	0.249452	synonymous-codon, nc-transcript-variant	KMT2B	GRCh38.p7	19:35727577	CCAGGTGCTCCAGGG[C/T]CTGCTGAGCTCCAAG	9757
rs11670996	snp	A/C			missense	KMT2B	GRCh38.p7	19:35732977	CGGCGCCTCCCCTGG[A/C]TAATGGCAGCCAGCC	9757
rs11672164	snp	A/G	0.292523	0.246357	intron-variant	KMT2B	GRCh38.p7	19:35725142	GGAAGAACCTCGATG[A/G]CTGTGTCATCGAGAA	9757
rs12459634	snp	C/T	0.398393	0.201195	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	IGFLR1, KMT2B	GRCh38.p7	19:35739273	CAGCAAAGTTCTTTA[C/T]TGGGTGTTAAGCCCA	9757
rs12463059	snp	C/T	0.225005	0.248747	upstream-variant-2KB, downstream-variant-500B	KMT2B, ZBTB32	GRCh38.p7	19:35717547	GGGCCTCGGGGGTCC[C/T]GGGGCCCGAGCCCGC	9757
rs12610493	snp	A/C	0	0	intron-variant	KMT2B	GRCh38.p7	19:35733578	ATGCGGCTCATCCTT[A/C]TCGGGCTCGCCCTCC	9757
rs12610518	snp	A/C	0	0	intron-variant	KMT2B	GRCh38.p7	19:35733742	CTGTCCTTCCCCTTC[A/C]TGACAGGTCTCTTCT	9757
rs12981566	snp	C/T	0.0189856	0.0955633	downstream-variant-500B, upstream-variant-2KB	ZBTB32, KMT2B	GRCh38.p7	19:35717440	CACCGTGCCAAGCCG[C/T]CGCCAGGTCGCGCCT	9757
rs12984350	snp	A/T	0.0433465	0.140692	intron-variant	KMT2B	GRCh38.p7	19:35735011	GTGCGGGACACAGAC[A/T]TGTTAGCAAGGGCAG	9757
rs16970648	snp	C/T	0.151001	0.229563	intron-variant	KMT2B	GRCh38.p7	19:35726432	GGCTTTAGCACAGAC[C/T]CTCTTTTCTCATGGC	9757
rs16970649	snp	C/T	0.195877	0.244071	missense	KMT2B	GRCh38.p7	19:35731956	CAGATGTTCTTGTCC[C/T]TGGAGCTCCTGAGCG	9757
rs17776911	snp	C/T	0.296873	0.245566	intron-variant	KMT2B	GRCh38.p7	19:35734072	ATGACATTTCGCCTC[C/T]ACGTGGGATCCTTTT	9757
rs28373672	snp	A/G	0.454182	0.144256	intron-variant, upstream-variant-2KB	KMT2B	GRCh38.p7	19:35722170	TCACCACGCCTGGCT[A/G]ATTTTTGTATTTTTA	9757
rs34014681	snp	A/G	0.0221895	0.102968	synonymous-codon, nc-transcript-variant	KMT2B	GRCh38.p7	19:35723964	AGCAGGGGGGCCCCC[A/G]GGCTCCGAGTCATCC	9757
rs34031911	snp	G/T	0.254105	0.249966	intron-variant	KMT2B	GRCh38.p7	19:35718798	GGCCTCGCAACCTCC[G/T]GGTTTCTCCAGGGCC	9757
rs34078597	in-del	-/G			frameshift-variant, nc-transcript-variant	KMT2B	GRCh38.p7	19:35727555	GGGCCCTCCAGGGGG[-/G]CCTGCGCCAGGTGCT	9757
rs34083627	in-del	-/G			intron-variant, upstream-variant-2KB	KMT2B	GRCh38.p7	19:35722728	AGAGGGTAGGTGGGG[-/G]AGACTGGACAGCCAT	9757
rs34125691	in-del	-/G			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	ZBTB32, KMT2B	GRCh38.p7	19:35717021	CATAATAAAGAGTTT[-/G]CCTGTGCCCTCCCTT	9757
rs34234254	snp	A/G	0.022776	0.104256	intron-variant	KMT2B	GRCh38.p7	19:35730192	CACTTAGGGACCCCC[A/G]TGGCCCCCAGGCCTG	9757
rs34241915	in-del	-/A			frameshift-variant, upstream-variant-2KB, nc-transcript-variant	KMT2B	GRCh38.p7	19:35721691	TTGCGGGCGTGGGTT[-/A]CCTTGCCGCTGTCTG	9757
rs34515466	in-del	-/A	0	0	intron-variant	KMT2B	GRCh38.p7	19:35727004	AAAAAAAAAAAAAAA[-/A]GCCTCATCCTCAAGG	9757
rs34743105	in-del	-/C			intron-variant	KMT2B	GRCh38.p7	19:35723720	TCCTACTAAGTCCCC[-/C]TGTTCCCGCAGGCCG	9757
rs34763514	in-del	-/C			intron-variant	KMT2B	GRCh38.p7	19:35723684	CTCTCCCAGTGTCCC[-/C]ATGTCCCTGGCTGAG	9757
rs34827551	in-del	-/T	0.253824	0.249971	downstream-variant-500B, upstream-variant-2KB	ZBTB32, KMT2B	GRCh38.p7	19:35717140	CAGCGGGATGGACAC[-/T]TTCTTCCACCCCCGA	9757
rs34836941	in-del	-/G			intron-variant	KMT2B	GRCh38.p7	19:35725920	GAGCAGAGGTTGGGG[-/G]ATCCTCTTAAGAATT	9757
rs34980546	snp	A/G	0.00221627	0.0332148	synonymous-codon	KMT2B	GRCh38.p7	19:35730452	CTTACCAATGAGCAC[A/G]TTGATGGCATCGGGT	9757
rs35021476	in-del	-/G			frameshift-variant	KMT2B	GRCh38.p7	19:35737697	GTGCTCCCTGAGGGG[-/G]CCACCTGTGATGAGG	9757
rs35284788	in-del	-/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	IGFLR1, KMT2B	GRCh38.p7	19:35738928	GTAGGAACCCCACTT[-/T]CTACACACCCACCCA	9757
rs35920945	in-del	-/C			intron-variant	KMT2B	GRCh38.p7	19:35730285	CTGTTCAGACTTCCC[-/C]TGGCATCCACCTCCC	9757
rs36062432	snp	G/T	0.471655	0.115624	missense	KMT2B	GRCh38.p7	19:35736754	ATGTGGGCCAGTCCG[G/T]TTTGGGGCCTGGTTC	9757
rs55836857	in-del	-/T			intron-variant, upstream-variant-2KB	KMT2B	GRCh38.p7	19:35722004	CTGTCCCTATCTTCC[-/T]TTTTTTTTTTTTTTT	9757
rs56792854	snp	C/G	0.154993	0.231244	intron-variant	KMT2B	GRCh38.p7	19:35737488	GGAGTTGGAGACCAG[C/G]GTAGGCAACATGGCA	9757
rs57143153	in-del	-/ATCAGGGTCTGG			intron-variant	KMT2B	GRCh38.p7	19:35724898	TGGATCAGGGTCTGG[-/ATCAGGGTCTGG]GTCCAGTAGGCTGGG	9757
rs57853545	snp	C/G	0.0182019	0.0936463	intron-variant	KMT2B	GRCh38.p7	19:35737507	GGCAACATGGCAAAA[C/G]CCCATCTCTAAAATA	9757
rs58103380	snp	C/T	0.113685	0.209567	intron-variant	KMT2B	GRCh38.p7	19:35729587	CTCTCACTACATCCC[C/T]GTGAGGTTAGAATTC	9757
rs58280237	snp	C/T	0.000381265	0.0138017	intron-variant	KMT2B	GRCh38.p7	19:35730336	CTTTGCCACCCCCTC[C/T]TCCAGGAAATTGTGA	9757
rs59075654	snp	A/C/G	0.00874735	0.0655527	intron-variant	KMT2B	GRCh38.p7	19:35735726	TCAGCCTGTCCCAAA[A/C/G]TGAGCCCTCCACCTG	9757
rs60207923	snp	C/T	0.000830107	0.0203559	missense, utr-variant-5-prime, nc-transcript-variant	KMT2B	GRCh38.p7	19:35719862	CAGATGTGGCTCCTA[C/T]CCCCCCAAAGACCCC	9757
rs61351824	snp	A/C/G	0.411428	0.266864	intron-variant	KMT2B	GRCh38.p7	19:35732210	CACCAACCCTCCCCC[A/C/G]ACAGGAAGTCCATCT	9757
rs61740785	snp	C/T	0.000248674	0.0111479	synonymous-codon, nc-transcript-variant	KMT2B	GRCh38.p7	19:35728124	TGCGTTCGGCTGGTT[C/T]GACGCCCACGACCCC	9757
rs61743066	snp	C/T	0.000364848	0.0135015	synonymous-codon, missense	KMT2B	GRCh38.p7	19:35738107	TAAGCGCAACATCGA[C/T]GCGGGGGAGATGGTC	9757
rs61746997	snp	C/G	0.00139317	0.0263561	missense, nc-transcript-variant	KMT2B	GRCh38.p7	19:35724681	AGCCGGCCCCGCAAA[C/G]CTACCCTGCAGCCTG	9757
rs61746999	snp	C/T	0.0014994	0.0273396	synonymous-codon, nc-transcript-variant	KMT2B	GRCh38.p7	19:35724686	GCCCCGCAAACCTAC[C/T]CTGCAGCCTGTGTTG	9757
rs66747537	snp	A/G	0.295854	0.245759	intron-variant	KMT2B	GRCh38.p7	19:35729529	GAAGAGTGCCCATTG[A/G]TTGAACCTGGGCTGC	9757
rs73048513	snp	C/T	0.0865458	0.189163	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	ZBTB32, KMT2B	GRCh38.p7	19:35716991	TAACAGTAGGGGAGA[C/T]TGTCGATCTCATCAC	9757
rs73048518	snp	A/G	0.0799831	0.183287	intron-variant	KMT2B	GRCh38.p7	19:35726612	TTCCTGGAACCTCAC[A/G]TCTCCATTGAGCGGT	9757
rs73590576	snp	G/T	0.185788	0.241613	intron-variant	KMT2B	GRCh38.p7	19:35718879	GCTCGGGTTGAACAG[G/T]AGTGGGATGAAGGCC	9757
rs73590580	snp	C/T	0.00595561	0.0542433	intron-variant	KMT2B	GRCh38.p7	19:35727685	CAGCCCTGCTAACTT[C/T]CCCGCTTTGCAGTGT	9757
rs73590585	snp	A/G	0.227729	0.249006	synonymous-codon	KMT2B	GRCh38.p7	19:35732846	GGTCCTTGGGGCTGC[A/G]GGGGACAGGGCCCGG	9757
rs73590591	snp	A/G	0.181978	0.240568	intron-variant	KMT2B	GRCh38.p7	19:35735520	GGCCTTGACTTCTGT[A/G]TATGCTCACTCCCAG	9757
rs73590594	snp	C/T	0.0252325	0.109451	intron-variant	KMT2B	GRCh38.p7	19:35736237	GCCTGGGAGACAGAA[C/T]GAGACTTTGTCTCAA	9757
rs73590598	snp	C/T	0.229519	0.24916	intron-variant	KMT2B	GRCh38.p7	19:35737766	GTGTGAGCTGGGGGG[C/T]GGGTGGTGGTCTGGA	9757
rs73928306	snp	C/T	0.0174175	0.0916809	intron-variant	KMT2B	GRCh38.p7	19:35730927	AACAAACCTACAGAT[C/T]TCTGTTCCCCGCTCC	9757
rs74723295	snp	C/G	3.41268e-05	0.00413064	intron-variant	KMT2B	GRCh38.p7	19:35730879	TCAGGTGTGGCTTTG[C/G]CTCTGTCTTCTTCCT	9757
rs74785939	snp	C/T			missense, utr-variant-5-prime, nc-transcript-variant	KMT2B	GRCh38.p7	19:35723202	ACACAGGACCCACAG[C/T]CCTGCACACGTAGGC	9757
rs75055738	snp	C/G/T	0.039522	0.134904	intron-variant	KMT2B	GRCh38.p7	19:35729395	TCCCTACCTGGCATC[C/G/T]TTTCACTGCCAGGCT	9757
rs75245933	snp	A/G	0.0391387	0.134304	intron-variant	KMT2B	GRCh38.p7	19:35728519	GTACCTGCTGGAGCC[A/G]AGGTGTCAGGGAAGG	9757
rs75291651	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2B	GRCh38.p7	19:35737373	GGGAGGAGACACTAG[A/G]TCACTTGAAGAGTTA	9757
rs76025946	snp	A/G	0.0266528	0.112321	synonymous-codon, nc-transcript-variant	KMT2B	GRCh38.p7	19:35720457	AGAAGAGAAGAAAGA[A/G]GAAGAAGAAAAAGAC	9757
rs76288067	snp	A/G			missense, nc-transcript-variant	KMT2B	GRCh38.p7	19:35720083	GCAGAAGCAGCTGTG[A/G]CAATCCCCAAACCTG	9757

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