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
rs209022	snp	A/C	0.483199	0.0901004	intron-variant	KMT2C	GRCh38.p7	7:152278759	ATATTTCATAATAAC[A/C]TAAGTTTTATGTTAC	58508
rs466821	snp	C/G	0	0	intron-variant	KMT2C	GRCh38.p7	7:152216148	TCTCAACTGGTGGTC[C/G]CAGATCGACCATCAC	58508
rs594178	snp	C/T	0.248979	0.249998	synonymous-codon, nc-transcript-variant	KMT2C	GRCh38.p7	7:152248130	TGATGATGAAAATGA[C/T]GACTCTGTCTCAGAT	58508
rs887184	snp	A/C	0.48	0.0979796	intron-variant	KMT2C	GRCh38.p7	7:152406148	CCATTTTTGATATCT[A/C]AAATCTTTCATCATA	58508
rs887185	snp	C/T	0.486111	0.0821678	intron-variant	KMT2C	GRCh38.p7	7:152405142	ACATTTTTGGTGggg[C/T]gtggtgcctcatgcc	58508
rs910356	snp	C/T	0.375	0.216506	intron-variant	KMT2C	GRCh38.p7	7:152406132	ATATGGCTGACTAAA[C/T]TATGATGAAAGATTT	58508
rs940235	snp	G/T			intron-variant	KMT2C	GRCh38.p7	7:152283961	ATGTTATTGCTTTTT[G/T]CTATCTTTTTTTGAG	58508
rs1053342	snp	A/C	0	0	utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB	KMT2C, LOC731075	GRCh38.p7	7:152134957	CAGATTTAGAAGATC[A/C]CCATTTACAAATAAA	58508
rs1054694	snp	A/G	0	0	synonymous-codon, nc-transcript-variant	KMT2C	GRCh38.p7	7:152162765	GGAAAAAGGGAAAAA[A/G]AAAAGAACAAGAAAG	58508
rs1055978	snp	A/T	0.0707826	0.174302	intron-variant	KMT2C	GRCh38.p7	7:152369032	cctggccCTTAACTA[A/T]TTTTTTTTTTTAACC	58508
rs1057736	snp	A/T	0	0	intron-variant	KMT2C	GRCh38.p7	7:152159197	TGACACCACTCTATC[A/T]TCCCTACTTATTTAA	58508
rs1060764	snp	A/G	0.375	0.216506	intron-variant	KMT2C	GRCh38.p7	7:152244387	CTGGCCCATTTTTCA[A/G]CATTTTTATAGGTGT	58508
rs1060765	snp	C/T	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152244381	CATTTTTCAGCATTT[C/T]TATAGGTGTATGTAC	58508
rs1060766	snp	A/G	0.00481925	0.0488508	intron-variant	KMT2C	GRCh38.p7	7:152244373	AGCATTTTTATAGGT[A/G]TATGTACTTTGCGAC	58508
rs1060767	snp	A/G	0.375	0.216506	intron-variant	KMT2C	GRCh38.p7	7:152244367	TTTATAGGTGTATGT[A/G]CTTTGCGACCTGGGT	58508
rs1060768	snp	A/C	0.277778	0.248452	intron-variant	KMT2C	GRCh38.p7	7:152244327	TGATTATTGACACTG[A/C]CACATATTGTAATCA	58508
rs1060769	snp	A/G	0	0	intron-variant	KMT2C	GRCh38.p7	7:152244280	AACATCAAGCTAATG[A/G]CCCTACCCTAGACCA	58508
rs1060770	snp	C/T	0.0187777	0.0950591	intron-variant	KMT2C	GRCh38.p7	7:152244219	CTGTAACCCTGAAAG[C/T]GGAGTTCTGAACTAG	58508
rs1060771	snp	C/T	0	0	intron-variant	KMT2C	GRCh38.p7	7:152244213	CCCTGAAAGCGGAGT[C/T]CTGAACTAGAGAAAT	58508
rs1060772	snp	A/C	0	0	intron-variant	KMT2C	GRCh38.p7	7:152244159	TAAAAATGCATTAAA[A/C]TGAATACTGTAAGGA	58508
rs1060773	snp	G/T	0	0	intron-variant	KMT2C	GRCh38.p7	7:152244157	AAAATGCATTAAACT[G/T]AATACTGTAAGGAAT	58508
rs1060774	snp	A/G	0	0	intron-variant	KMT2C	GRCh38.p7	7:152244150	ATTAAACTGAATACT[A/G]TAAGGAATGCTCTTT	58508
rs1077139	snp	C/T	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152406153	CCAGCCCATTTTTGA[C/T]ATCTCAAATCTTTCA	58508
rs1133176	snp	A/G	0	0	intron-variant	KMT2C	GRCh38.p7	7:152294159	GATGTGGCTGGGCAT[A/G]GTGGCTCACACCTGT	58508
rs1133177	snp	A/G	0	0	intron-variant	KMT2C	GRCh38.p7	7:152294142	tggctcacacctgta[A/G]tcccagcactttggg	58508
rs1134342	snp	A/G			intron-variant	KMT2C	GRCh38.p7	7:152369148	tttagtggagacagg[A/G]ttttgccatgttggc	58508
rs1137721	snp	A/G	0.473634	0.111748	intron-variant	KMT2C	GRCh38.p7	7:152301320	agatggagtttcacc[A/G]tgtgggccaggctgg	58508
rs1137877	snp	C/T	0	0	intron-variant	KMT2C	GRCh38.p7	7:152244455	GCCTCAAGCGATCCT[C/T]CCATCTCGGGTCTCC	58508
rs1137878	snp	A/G	0.277778	0.248452	intron-variant	KMT2C	GRCh38.p7	7:152244307	TATTGTAATCAACTC[A/G]GTAGATTTTAGAACA	58508
rs1138663	snp	G/T	0.307671	0.243257	intron-variant	KMT2C	GRCh38.p7	7:152226311	TGGGAGGCGGAGGTT[G/T]TAGTGAGCTGAGATC	58508
rs1138664	snp	C/T	0.307423	0.243316	intron-variant	KMT2C	GRCh38.p7	7:152226310	GGGAGGCGGAGGTTT[C/T]AGTGAGCTGAGATCA	58508
rs1318346	snp	A/T	0.375	0.216506	intron-variant	KMT2C	GRCh38.p7	7:152406098	AGACAAAATAGTTTT[A/T]AAAAAAATTCTAGGA	58508
rs1328763	snp	A/T	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152412840	TTTTATAGATCTGAA[A/T]AAAGTAATTTCTTGA	58508
rs1623137	snp	A/T	0.184445	0.241252	intron-variant	KMT2C	GRCh38.p7	7:152247876	TTCCAATATCTTTTC[A/T]GTCAATATCATTAAA	58508
rs1640148	snp	C/T	0.5	0	intron-variant, utr-variant-5-prime	KMT2C	GRCh38.p7	7:152286337	cccaagcaggatgaa[C/T]acaaagaaaaccaca	58508
rs1640149	snp	G/T	0.46875	0.121031	intron-variant, upstream-variant-2KB	KMT2C	GRCh38.p7	7:152286389	ctgctgaaaaccaaa[G/T]ataaagagaaaatcc	58508
rs1730337	snp	C/G/T	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152289979	atctcagctcacttc[C/G/T]gtctcctgggttcaa	58508
rs1807595	snp	A/C/G	0.58	0.116619	intron-variant	KMT2C	GRCh38.p7	7:152412265	AATTAGCCGGGCATC[A/C/G]TGGCAGGAACCTGTA	58508
rs1807596	snp	A/G	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152412326	gaatggcttgaaccc[A/G]ggaggcggaggttgc	58508
rs1808264	snp	A/G	0.459184	0.136902	intron-variant	KMT2C	GRCh38.p7	7:152405931	GCGCACATGATCTTG[A/G]CTCACTGCAACCTCT	58508
rs1808265	snp	C/T	0.42	0.183303	intron-variant	KMT2C	GRCh38.p7	7:152405919	TTGACTCACTGCAAC[C/T]TCTGCCTCCCAGGTT	58508
rs1808266	snp	A/G	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152405404	TACAAAAATTAGCCA[A/G]GTGTGGTGGTGCATG	58508
rs1808267	snp	C/T	0.35503	0.226867	intron-variant	KMT2C	GRCh38.p7	7:152405371	TATAATCCCAGCTAC[C/T]TGGGAGGCTGAGGCA	58508
rs1808268	snp	G/T	0.489796	0.070696	intron-variant	KMT2C	GRCh38.p7	7:152405235	CTAAATTTAGATCTG[G/T]TGAGTTTGAAATGAT	58508
rs1810525	snp	C/T	0.486111	0.0821678	intron-variant	KMT2C	GRCh38.p7	7:152405107	CACCCGCCTTGGCCT[C/T]CCAAAATGGCAGGAT	58508
rs1810527	snp	A/C/T	0.000399281	0.0141238	intron-variant	KMT2C	GRCh38.p7	7:152405944	AGTCAAGATCATGTG[A/C/T]GCCATTGCACTCCAA	58508
rs1810528	snp	A/G	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152406064	GTATGTAAAACTACA[A/G]AGTAATAGCTTGATA	58508
rs1810802	snp	G/T			intron-variant	KMT2C	GRCh38.p7	7:152405898	ctcccaggttcaagc[G/T]attctcctccctcag	58508
rs1819336	snp	C/T	0.46875	0.121031	intron-variant	KMT2C	GRCh38.p7	7:152403410	gtgattctcctgcct[C/T]agcctcccaagtagc	58508
rs1819337	snp	C/T	0	0	intron-variant	KMT2C	GRCh38.p7	7:152403386	aagtagctgggatta[C/T]aggcacatggcacca	58508
rs1831136	snp	A/G	0	0	intron-variant	KMT2C	GRCh38.p7	7:152409892	TATACCTGAATCAGT[A/G]TTCTTTCAGAGACTT	58508
rs1831203	snp	C/G			intron-variant	KMT2C	GRCh38.p7	7:152408182	tcatgcctcagcctc[C/G]caagtggctgagatt	58508
rs1831205	snp	A/G	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152408171	CCTCCCAGGTGGCTG[A/G]GATTACAGGCACACG	58508
rs1831206	snp	C/T			intron-variant	KMT2C	GRCh38.p7	7:152408067	CTCCTGACCTTGTGA[C/T]CTGCCCACCTCGGCC	58508
rs1832353	snp	C/G	0	0	intron-variant	KMT2C	GRCh38.p7	7:152238257	CTTCAAGGACTGGCA[C/G]AGCCATCAACCAATG	58508
rs1833118	snp	A/G	0.059645	0.162065	intron-variant	KMT2C	GRCh38.p7	7:152412926	TTTAGTGGGATTCCT[A/G]TATCATTGTAGATTT	58508
rs1833119	snp	C/T	0.46281	0.131194	intron-variant	KMT2C	GRCh38.p7	7:152412699	CAAGACCACTGTGCA[C/T]TTAAGCTAGTTTATT	58508
rs1833120	snp	C/T	0.48	0.0979796	intron-variant	KMT2C	GRCh38.p7	7:152412635	ACGTTGTTTCTTTTT[C/T]TGTTGTTTGGTGTCA	58508
rs1833121	snp	A/G	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152407791	AGTTGTTTTGGGCAC[A/G]TATTTTCAACTTCTA	58508
rs1854367	snp	A/G	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152412754	CCCACCACAATATTT[A/G]AAGTGTTTAAATCAT	58508
rs1854368	snp	C/T	0.0233068	0.105405	intron-variant	KMT2C	GRCh38.p7	7:152412683	TTAAGCTAGTTTATT[C/T]GTTTATTAAAACAAA	58508
rs1961880	snp	C/G	0.46875	0.121031	intron-variant	KMT2C	GRCh38.p7	7:152405099	aagcaagccacccgc[C/G]ttggccttccaaagt	58508
rs1961881	snp	C/G			intron-variant	KMT2C	GRCh38.p7	7:152405308	CTGGAGTAGTGGCTC[C/G]ATCTCTGCTCACTGC	58508
rs1961882	snp	A/G	0	0	intron-variant	KMT2C	GRCh38.p7	7:152405127	agtgccgggattaca[A/G]gcatgaggcaccacg	58508
rs1961883	snp	A/G	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152405402	gacatgcaccaccac[A/G]cctggctaatttttg	58508
rs1961884	snp	C/T	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152405358	CAAGTGATTCTCATG[C/T]CTCAGCCTCCCAAGT	58508
rs1964159	snp	C/T	0	0	intron-variant	KMT2C	GRCh38.p7	7:152245117	CTAAACCATTTGTTG[C/T]TGCAACAAATCTTTC	58508
rs1972226	snp	A/T	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152412408	CAACATTAAAAAAAT[A/T]TTTTTTTGAGAGGGA	58508
rs1986374	snp	A/G	0	0	intron-variant	KMT2C	GRCh38.p7	7:152305941	ttctcaatgctactg[A/G]ggtgtcattgtttct	58508
rs1986375	snp	A/C/G	0.0607341	0.163335	intron-variant	KMT2C	GRCh38.p7	7:152306170	TCTACAGTTACTTAG[A/C/G]TGAGTTCTTTCCCTC	58508
rs1987049	snp	C/T	0.030665	0.119967	intron-variant	KMT2C	GRCh38.p7	7:152257304	tGAAAATAAGAGCAA[C/T]ATATCTTCTTATTCT	58508
rs2001482	snp	A/G	0.0197687	0.0974348	intron-variant	KMT2C	GRCh38.p7	7:152405942	GGAGTGCAATGGCGC[A/G]CATGATCTTGACTCA	58508
rs2003991	snp	C/T			intron-variant	KMT2C	GRCh38.p7	7:152405928	catgtgatcttggct[C/T]actgcaacttccgcc	58508
rs2013440	snp	C/T			intron-variant	KMT2C	GRCh38.p7	7:152318457	accccctccccattt[C/T]tactaaaaatacaaa	58508
rs2013442	snp	C/T			intron-variant	KMT2C	GRCh38.p7	7:152318455	ccaccccctccccat[C/T]tttactaaaaataca	58508
rs2024151	snp	C/G	0.284209	0.247648	intron-variant	KMT2C	GRCh38.p7	7:152410891	tcagcctcccaagta[C/G]ctggggccgtgggga	58508
rs2026700	snp	A/G	0	0	intron-variant	KMT2C	GRCh38.p7	7:152406120	ATAGTTTAGTCAGCC[A/G]TATTTTTCCTAGAAT	58508
rs2038262	snp	C/G	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152404862	gttttgttttgtttt[C/G]ttttttgagataggg	58508
rs2038263	snp	A/G	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152405056	gggtttcttcatgtt[A/G]cccagctggtctcaa	58508
rs2077625	snp	A/G	0.48	0.0979796	intron-variant	KMT2C	GRCh38.p7	7:152405852	GAATTACAGCCATGC[A/G]CCACCATGCCTAGCT	58508
rs2078405	snp	A/G	0.0267878	0.112589	intron-variant	KMT2C	GRCh38.p7	7:152227371	CCAAAGTTGTTACAG[A/G]TATGTTTTATAATCT	58508
rs2078626	snp	C/T	0.375	0.216506	intron-variant	KMT2C	GRCh38.p7	7:152405489	gtcccatgtgatctg[C/T]ccaccttggcctccc	58508
rs2078659	snp	C/T	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152413199	acctcactacagcct[C/T]gacctcctgggttca	58508
rs2078660	snp	A/T	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152413329	catgctgcacagact[A/T]gttgagctcctgagc	58508
rs2078661	snp	A/G	0.5	0	intron-variant	KMT2C	GRCh38.p7	7:152413356	gagctcaagcaatcc[A/G]cccgcctcagcctcc	58508
rs2098219	snp	C/T			intron-variant	KMT2C	GRCh38.p7	7:152216696	CATGGAAACATTAAG[C/T]TCATAGAATAATTGT	58508
rs2108907	snp	A/G			intron-variant	KMT2C	GRCh38.p7	7:152431529	aacttccgcctccca[A/G]gttcaagtgattctc	58508
rs2108908	snp	G/T	0.448066	0.152544	intron-variant	KMT2C	GRCh38.p7	7:152415704	TTTAGTAGAAATGGG[G/T]TTTCACTATGTTGGC	58508
rs2144090	snp	A/G	0.444444	0.157135	intron-variant	KMT2C	GRCh38.p7	7:152406162	TGAGATATCAAAAAT[A/G]GGCTGGGTGCAGCTG	58508
rs2192029	snp	C/G			intron-variant	KMT2C	GRCh38.p7	7:152210320	GCACCACCACATACA[C/G]AAAGCTTTCTAATCA	58508
rs2240819	snp	C/T	0.132476	0.220654	intron-variant	KMT2C	GRCh38.p7	7:152145312	TGAAAAGAAGCAAAG[C/T]AGACACAAAGTCACC	58508
rs2259334	snp	A/G	0.375	0.216506	intron-variant	KMT2C	GRCh38.p7	7:152244913	TGAAAGGAAAAATAC[A/G]AAAAACTAAACTTTA	58508
rs2270234	snp	C/G	4.9423e-05	0.00497082	missense, nc-transcript-variant	KMT2C	GRCh38.p7	7:152177655	TGTGTCTAGGGCCCG[C/G]AAAGTCTGGCCGGGG	58508
rs2302478	snp	C/T	0.00021446	0.010353	synonymous-codon, intron-variant, nc-transcript-variant	KMT2C	GRCh38.p7	7:152220563	CCTTGAATGCTCTGA[C/T]TGGATGTCTGGAGGG	58508
rs2360208	snp	C/T	0.408163	0.193609	intron-variant	KMT2C	GRCh38.p7	7:152412160	cctgccttggcctcc[C/T]aaactgctgggatta	58508
rs2360210	snp	A/G	0.453575	0.145111	intron-variant	KMT2C	GRCh38.p7	7:152386065	gagtctcattctgtc[A/G]ctcgggctggagtgc	58508
rs2360211	snp	A/G			intron-variant	KMT2C	GRCh38.p7	7:152384069	TCTacatgcacacgc[A/G]cctacacacacgcac	58508
rs2360212	snp	A/G	0.305934	0.243663	intron-variant	KMT2C	GRCh38.p7	7:152384057	CGCGCCTACACACAC[A/G]CACACACACACAGAC	58508
rs2360213	snp	C/T			intron-variant	KMT2C	GRCh38.p7	7:152384036	acacacagacacaca[C/T]GTCTGCCTCTCGGAT	58508
rs2360214	snp	C/T	0	0	intron-variant	KMT2C	GRCh38.p7	7:152383911	AAAAGTTGCTGCTCC[C/T]GTCCTAGCAGCACAA	58508

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