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
rs111680	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118447986	AGTCCTGCCTACATA[A/T]GTATAAAATGACCTC	4297
rs111681	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118447988	TCCTGCCTACATATG[A/T]ATAAAATGACCTCTT	4297
rs125315	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118441562	GTTATTTTCAGTCTA[C/G]GTGGTATATTCCTGT	4297
rs471239	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118449309	acaactgtaatacca[C/G]cactgtgggaggctg	4297
rs471380	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118453272	agctatttcagaggc[A/T]tcatggggataaaag	4297
rs471406	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118453270	ctatttcagaggcat[C/T]atggggataaaagcc	4297
rs472368	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118453140	atcaggtagcagcta[A/G]aggtggacgtggggt	4297
rs474155	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118468058	TGGAAAGGACAAAAA[A/G]CAAAAGCTTCTGCTT	4297
rs474257	snp	C/T	0.00676609	0.0577691	intron-variant	KMT2A	GRCh38.p7	11:118468021	AATTTTAACCTGCTC[C/T]ATAAAAAAAAAAAGG	4297
rs475993	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118452761	ctgtaatcccagcta[A/C]ttgggaggctgaggc	4297
rs476767	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118452690	gccgagatggcgcca[A/C]tgcactccagcctgg	4297
rs476793	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118452685	gatggcgccactgca[A/C]tccagcctgggcagt	4297
rs476868	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118452654	agagtgagactccat[C/T]tcaaaaaTTTTACCA	4297
rs477101	snp	A/G	0.00755907	0.0610114	intron-variant	KMT2A	GRCh38.p7	11:118492703	AAAAGAAGAAGAACC[A/G]CATGGATCACTTTAC	4297
rs477106	snp	A/C	0.4661	0.125701	intron-variant	KMT2A	GRCh38.p7	11:118492709	AGAAGAACCGCATGG[A/C]TCACTTTACCTCAGA	4297
rs477901	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118449137	AATGTGGGCTTCTCA[C/G]AATGTGATGGCAAAC	4297
rs478056	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118467585	ACAAATTAGCAGGTT[C/T]ATCTCTTAAATTTAA	4297
rs478923	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118469752	GCTGTTTCTGCTTTT[A/T]GACATTGACTTAGCT	4297
rs480925	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118444300	CAAACATTGTCCCTA[A/G]ATTATTGCCCTTAAT	4297
rs487396	snp	A/C	0.104938	0.20361	intron-variant	KMT2A	GRCh38.p7	11:118463423	ATGCATTTCACAAAG[A/C]CATCTGGGGATTTCC	4297
rs488696	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118442807	CCTGGAAACTAAAGT[C/T]AAACTACTTTTTCCA	4297
rs490330	snp	C/G	0.225766	0.248823	intron-variant	KMT2A	GRCh38.p7	11:118506821	ATGTAACAAAATGTA[C/G]TTCCATCCATGGGCA	4297
rs490946	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118509377	ATGTACTGGAAGAAC[A/C]CTGCACCGAGAGACA	4297
rs490968	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118509365	AACACTGCACCGAGA[A/G]ACAGGTGCGCCAAGT	4297
rs492927	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118463421	TGGGAAATCCCCAGA[A/T]GTCTTTGTGAAATGC	4297
rs493699	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118486324	GGAAGGATTCACACC[A/C]AAATATTAAAAGTGT	4297
rs493992	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118456332	aaaGGTTCATttttt[A/T]aatttttagtagaga	4297
rs495132	snp	C/T	0.412917	0.189626	intron-variant	KMT2A	GRCh38.p7	11:118465212	tttcactctgtcacc[C/T]agctatagtgcagtg	4297
rs496223	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118486537	TGGCAGATACCTCTT[G/T]GGCTTATTACTTACC	4297
rs497209	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118464949	tactacaaaaatgcc[A/C]aggaaagcttcacca	4297
rs497242	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118464939	ttcctgggcattttt[C/G]tactaaagctttggt	4297
rs497478	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118444324	ATCCACAAGGTTTTA[C/G]TGCTTATAATTAAAG	4297
rs498268	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118444256	AAGTGGTCAATCCTC[A/G]TGGATGGACAGAAGT	4297
rs498362	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118444230	GAAGTTGAATATGGG[C/G]ATGTGTAAATATTTC	4297
rs498684	snp	A/G	0.485255	0.0845871	intron-variant	KMT2A	GRCh38.p7	11:118446245	tcccagctacttggg[A/G]ggctgaggcatgaga	4297
rs499189	snp	A/T	0.384401	0.210799	intron-variant	KMT2A	GRCh38.p7	11:118486899	attttttaaattttt[A/T]aaaatttttttgaga	4297
rs500041	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118474436	ctgcaaataccactg[C/G]ctccaccatactttt	4297
rs500043	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118509345	TTGGCCCACATTGGA[C/T]TGAAACTTGGCGCAC	4297
rs500084	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118458876	GAACTAACAAAATTA[C/T]TGAGAACAACTAAAG	4297
rs500839	snp	A/T	0.0198	0.0975087	intron-variant	KMT2A	GRCh38.p7	11:118509393	GTTCTTCCAGTACAT[A/T]TTGTGTGATCACCTG	4297
rs502935	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118478740	ATGCATGAACATATT[C/T]TAAGAGAGAGTGAGA	4297
rs503076	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118478692	CAAGGTATCTCCAAT[G/T]TTTCCTGAATTGTCA	4297
rs503106	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118478678	TGTTTCCTGAATTGT[C/T]ATAATTTTGTTGGGT	4297
rs503691	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118461928	TGCTGCAAAAAAGTC[C/T]TCCTTTCACTGCACT	4297
rs503782	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118461892	GAGCAACAGGCTTCT[C/G]ATCTTGCTCCATCAC	4297
rs507291	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118478988	atagtaggtatatat[A/T]tttatggtatacata	4297
rs514924	snp	C/T	0.409382	0.192607	intron-variant	KMT2A	GRCh38.p7	11:118476148	GGAGGCCGAGGCGGG[C/T]AGATCACCTGAGGTC	4297
rs515934	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118465013	caaagtttgcccttt[G/T]tttgatgagaggaat	4297
rs516511	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118468002	CAAAATAGGTTAAAC[A/C]AATCCTTTTTTTTTT	4297
rs516676	snp	G/T	0	0	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525456	CTTAATTCTTGTTAT[G/T]GGTGTAAAAACAGAG	4297
rs517989	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118441889	AAGGTGAGCAAAGAG[A/G]TGAGAATTAAGTCAA	4297
rs518835	snp	A/G	3.56347e-05	0.00422091	missense	KMT2A	GRCh38.p7	11:118482090	CCTCCTCACTCACCT[A/G]ATTCTGGTGGTGGAG	4297
rs520124	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118496852	catctttaaaatgaa[A/G]ataataacgcttacc	4297
rs521816	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118441448	TACACATAGTTCTGA[A/G]AACCTACAGAATCCC	4297
rs524103	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118454957	ATATTCGCTAGGGTA[C/G]ACAGGAAAGGCTTCT	4297
rs524616	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118498551	CTTTTTTTTTTTTTT[A/T]AAAGCAACTAAAGCT	4297
rs524936	snp	A/G	0.416055	0.186885	intron-variant	KMT2A	GRCh38.p7	11:118471206	ATTGAAGAGCAGCGT[A/G]TTCAAATTTGTTCAA	4297
rs525174	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118446857	CAGATTCTCAGCGCT[C/G]CATGATCTTGCTAGC	4297
rs525177	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118446863	CTCAGCGCTGCATGA[G/T]CTTGCTAGCCTGTAT	4297
rs525549	snp	A/T	0.361684	0.223667	intron-variant	KMT2A	GRCh38.p7	11:118487353	GCATGCTATTCTCTA[A/T]TTTATATTTTAGGAA	4297
rs526168	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118441037	TGAGCTATTTAGTCC[A/C]AACttttcattttac	4297
rs528056	snp	C/T	0.400504	0.199621	intron-variant	KMT2A	GRCh38.p7	11:118447192	TAAAAAATTTAACCC[C/T]GTATACCTTATGTCG	4297
rs529378	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118486917	CCTAGCTTGGAtttt[C/T]ttattttttaaattt	4297
rs529862	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118471642	ATATATGCTCTTCAT[G/T]GTTTAATTTCTATAC	4297
rs530044	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118458272	caacatagtgaaacc[C/T]tctttctataaaaaa	4297
rs530300	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118478935	AACTTCTTAAAAAAA[A/G]AAATTTCATATGAGg	4297
rs531076	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118478906	Ggccaagcactgtgg[C/G]tcatgtttgtaatcc	4297
rs531723	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118459036	TGATTCATTGAAATT[G/T]GTTTTGTAATTGAAG	4297
rs532198	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118478743	CATATGCATGAACAT[A/T]TTCTAAGAGAGAGTG	4297
rs532536	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118459109	agagtcttgctctgt[C/T]acccaggctggagtg	4297
rs533942	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118478578	GAGCTACAgtctgat[A/T]tggtagccactagtt	4297
rs535327	snp	A/G	0.419135	0.184101	intron-variant	KMT2A	GRCh38.p7	11:118471070	CCACTGAGTTCAGTG[A/G]TCTTATTCTGATGTG	4297
rs536256	snp	C/T	0.489434	0.0719116	intron-variant	KMT2A	GRCh38.p7	11:118456606	TCATGCCTGTAATCC[C/T]AGCACTTTGGGAGGC	4297
rs537975	snp	C/T	0.479744	0.0985793	intron-variant	KMT2A	GRCh38.p7	11:118492154	GAGAAATTTGGACTT[C/T]ATACTCTGAAGGTGA	4297
rs538421	snp	C/T	0.0607341	0.163335	intron-variant	KMT2A	GRCh38.p7	11:118460440	aaatagctgggtgtg[C/T]tggtgcatgcctgtg	4297
rs538739	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118461877	ATGTGCTTAAGGAGA[A/G]TGATGGAGCAAGATG	4297
rs542117	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118467851	CCTTATTTTGTTCTT[A/G]TTTTATGTGGATTTT	4297
rs542195	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118469097	ctgcacccactaact[C/G]gtcatctagcattag	4297
rs542416	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118467426	GAAAAGGCTGAAATT[C/T]TCCTCTTCCAAGACA	4297
rs542534	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118498191	TATATCAATACTTGT[G/T]GGCTAACTACCCTGA	4297
rs543370	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118455874	tgtgaaaccccatct[C/G]tacaaagaaaaacac	4297
rs543872	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118468048	AATTAGAGGTAAGCA[C/G]AAGCTTTTGCTTTTT	4297
rs543875	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118444229	AAGTTGAATATGGGC[A/G]TGTGTAAATATTTCT	4297
rs545991	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118467040	AATTTAAGGAACACA[A/G]ACTACAGTAATTTTT	4297
rs546434	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118462516	ACTTTTACCCAAGAA[C/T]TTTCTTTGCACTTGA	4297
rs547745	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118455116	ttcatgtgagcccaa[C/G]agtttgaggctgcag	4297
rs552045	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118451398	aattttcttttctgt[C/T]ctcttttgagacaga	4297
rs552054	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118451405	ttttctgttctcttt[A/T]gagacagagtcttgc	4297
rs552738	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118461891	AGCAACAGGCTTCTC[A/G]TCTTGCTCCATCACT	4297
rs552991	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118451509	tctcgtgcctcagcc[C/T]cctgagtagctgaga	4297
rs554423	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118469074	tatacatgtgccatg[A/C]tggtgcgctgcaccc	4297
rs555878	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118486334	TAATCCAACCACACT[C/T]TTAATATTTTGGTGT	4297
rs555954	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118486307	GTGTGAATCCTTCCA[A/G]ATTGTTTTCTAGATA	4297
rs557465	snp	G/T	0	0	missense	KMT2A	GRCh38.p7	11:118501693	ATTTCAGCTGTGTTT[G/T]GACTCTCTTTGATGA	4297
rs557988	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118441705	TTATACTGAGCATTA[A/G]AAATTCAGTCTTTAG	4297
rs558086	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118453535	tgtgtagacagagaa[A/G]gcagtgaaaagtaga	4297
rs561775	snp	C/T	0.418814	0.184396	intron-variant	KMT2A	GRCh38.p7	11:118470497	GCAGAGAAACCATGT[C/T]TCATTTCTCAAATAA	4297
rs562780	snp	A/G	0.292953	0.246282	intron-variant	KMT2A	GRCh38.p7	11:118491699	GTCCTCTGAAGAATG[A/G]GAGAGAGGAAGAAGA	4297
rs562795	snp	C/T	0.027022	0.113052	intron-variant	KMT2A	GRCh38.p7	11:118464967	catgatggagcagga[C/T]tctggtgaagctttc	4297
rs562884	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118464936	ctgggcatttttcta[C/G]taaagctttggttaa	4297

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