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
rs1868	snp	C/G	0.225005	0.248747	intron-variant	KAT2B	GRCh38.p7	3:20148918	TACAGCAGTCAAGTA[C/G]TTTAATCTAACTTCT	8850
rs939851	snp	C/T	0.0952156	0.196321	intron-variant	KAT2B	GRCh38.p7	3:20086259	GCCTGGGTGACAGAG[C/T]GAGACACTGTCTCAA	8850
rs966898	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20142085	CTCTCAGCTAACACC[A/G]TGGGGATGAATTAGT	8850
rs977162	snp	A/G	0.249886	0.25	intron-variant	KAT2B	GRCh38.p7	3:20150014	AAGTAGGCTATGATC[A/G]ACGAGATCTGCTAGA	8850
rs1046039	snp	A/T			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20154259	ttaaaaattaatatt[A/T]tCTTATAGATATTGT	8850
rs1061636	snp	C/G	0.264632	0.249571	intron-variant	KAT2B	GRCh38.p7	3:20149235	CCATATTTTTGGAGA[C/G]AGCCAGAGTCTTCTG	8850
rs1062974	snp	A/T			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20154262	aaaattaatattttC[A/T]TATAGATATTGTGCA	8850
rs1124376	snp	A/G	0.152334	0.230133	intron-variant	KAT2B	GRCh38.p7	3:20067054	GAGACAACATGGGGT[A/G]AAACACTGAGAAGCA	8850
rs1138710	snp	A/C	0	0	intron-variant	KAT2B	GRCh38.p7	3:20149456	agctgtgattgcacc[A/C]ctgcacttcagcctg	8850
rs1610186	snp	G/T	0.444	0.157683	intron-variant	KAT2B	GRCh38.p7	3:20067152	TCCCAGTACAAAGTA[G/T]ATTTTTATTTCTTTT	8850
rs1879775	snp	A/T	0.254105	0.249966	intron-variant	KAT2B	GRCh38.p7	3:20081607	GCCCACCAAAAGGAA[A/T]AAACTTTGCCACAGC	8850
rs1915919	snp	C/T	0.400325	0.199756	intron-variant	KAT2B	GRCh38.p7	3:20042389	ATGAGAACAGGACAC[C/T]GACTGTAGTAGGCAG	8850
rs1915920	snp	A/G	0.172351	0.237636	intron-variant	KAT2B	GRCh38.p7	3:20042513	taaagaacttatgta[A/G]tcaaacaccacctgt	8850
rs1915921	snp	A/G	0.123798	0.215808	intron-variant	KAT2B	GRCh38.p7	3:20042583	CTTGGTGGCCTTGGC[A/G]TTTCGCAGCCAAAGT	8850
rs1915922	snp	C/T	0.311123	0.242413	intron-variant	KAT2B	GRCh38.p7	3:20042587	GTGGCCTTGGCGTTT[C/T]GCAGCCAAAGTGGGC	8850
rs1915923	snp	C/T	0.499965	0.00419314	intron-variant	KAT2B	GRCh38.p7	3:20047156	actagggtgggagga[C/T]cacctgagcccactg	8850
rs1986917	snp	C/G	0.45889	0.13735	intron-variant	KAT2B	GRCh38.p7	3:20077030	ATGTTCTTTGGAGCT[C/G]TGGTTTTGTGTAGTC	8850
rs2001650	snp	G/T	0.0923359	0.194016	intron-variant	KAT2B	GRCh38.p7	3:20041059	GCAACAAAACCCCAA[G/T]GTAGCCCGGGAGCTC	8850
rs2068477	snp	C/T	0.490943	0.0666801	intron-variant	KAT2B	GRCh38.p7	3:20151086	AAGACTCATCAAATC[C/T]CACACTAAATGTCCC	8850
rs2068668	snp	C/T	0.123105	0.215401	intron-variant	KAT2B	GRCh38.p7	3:20151209	TTGAATAAAGCCTAT[C/T]TTGGTTAGAGTGTAT	8850
rs2140084	snp	C/T	0.485118	0.0849685	intron-variant	KAT2B	GRCh38.p7	3:20076109	atcatgagccccttt[C/T]gatcatacctgagtt	8850
rs2140085	snp	A/C	0.216649	0.247765	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136623	AAAACTTTTATATTA[A/C]TATTCAGCAAGTGAT	8850
rs2293139	snp	A/G	0.0948562	0.196037	intron-variant	KAT2B	GRCh38.p7	3:20095016	ACATTATTTGCATAC[A/G]TTAGCCACCAGCCCA	8850
rs2293140	snp	C/T	0.499918	0.00638925	intron-variant	KAT2B	GRCh38.p7	3:20095119	AAGACTTCAGTCCTA[C/T]AGGAGTTCAGAAATT	8850
rs2293141	snp	A/T	0.499923	0.00618962	intron-variant	KAT2B	GRCh38.p7	3:20095153	TCTTATTACCAGTGA[A/T]CTTAAAGGATTGATG	8850
rs2293142	snp	G/T	0.434253	0.168969	intron-variant	KAT2B	GRCh38.p7	3:20095191	TGATGAAAGAGGACC[G/T]TCCACTTAAAAATGG	8850
rs2293143	snp	A/C	0.000161214	0.00897669	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20095402	AGTTTATTTCTATCT[A/C]TTTAAGGTGAGATTT	8850
rs2365361	snp	A/G	0.369754	0.219451	intron-variant	KAT2B	GRCh38.p7	3:20082305	CTCCCAGAGTGTTGG[A/G]ATTACAGGCTTGAGC	8850
rs2365362	snp	A/T	0.254105	0.249966	intron-variant	KAT2B	GRCh38.p7	3:20082385	ACTTTAGTAAATTTA[A/T]CATTAATATAATACC	8850
rs2365363	snp	A/T	0.451483	0.148002	intron-variant	KAT2B	GRCh38.p7	3:20085143	TTGCTTGAGCCCAGG[A/T]GTTTGAGACTAGCCT	8850
rs2365364	snp	A/T	0.490673	0.0676508	intron-variant	KAT2B	GRCh38.p7	3:20085199	TATGTCTATTAATTT[A/T]AAAAAAAAGTTTATA	8850
rs2365365	snp	A/T	0.490673	0.0676508	intron-variant	KAT2B	GRCh38.p7	3:20085200	ATGTCTATTAATTTA[A/T]AAAAAAAGTTTATAA	8850
rs2365367	snp	C/T	0.482979	0.0906686	intron-variant	KAT2B	GRCh38.p7	3:20074585	CTATCAGGGTTCTTT[C/T]ACTTCACACAGCAGA	8850
rs2365368	snp	C/G	0.497558	0.0348586	intron-variant	KAT2B	GRCh38.p7	3:20076202	aactgggacaaagac[C/G]aagtatatttcatac	8850
rs2365369	snp	A/G	0.497558	0.0348586	intron-variant	KAT2B	GRCh38.p7	3:20076232	ctataccacaAACAT[A/G]TATTTTAATATATAT	8850
rs2365370	snp	A/G	0.239326	0.249772	intron-variant	KAT2B	GRCh38.p7	3:20077488	GTAGCCACTGGCCAC[A/G]TGAAATGTGTTTACT	8850
rs2365371	snp	A/C	0.242488	0.249887	intron-variant	KAT2B	GRCh38.p7	3:20077651	ttgggttaatgtatt[A/C]ttaaaattatttcta	8850
rs2365375	snp	A/G	0.369958	0.21934	intron-variant	KAT2B	GRCh38.p7	3:20089544	tagctgagattacag[A/G]cgtgcgccaccatgc	8850
rs2365785	snp	C/T	0.441841	0.160303	intron-variant	KAT2B	GRCh38.p7	3:20093273	tctcactgtgggcaa[C/T]tggtactcaattctg	8850
rs2365790	snp	C/T	0.409721	0.192325	intron-variant	KAT2B	GRCh38.p7	3:20049127	GGCCTCTCAAAGTGC[C/T]GGGATTACAGGTGTG	8850
rs2365792	snp	A/G	0.439502	0.163061	intron-variant	KAT2B	GRCh38.p7	3:20111264	TTTACAGGTAAGGAA[A/G]GAAAGGCTAAATAGC	8850
rs2365793	snp	A/G	0.0944967	0.195752	intron-variant	KAT2B	GRCh38.p7	3:20111902	AAGAAACATTCCAAG[A/G]GGATGGGAGAAAAGA	8850
rs2365794	snp	C/T	0.432063	0.171327	intron-variant	KAT2B	GRCh38.p7	3:20114810	ATGTTAAGGTGATTG[C/T]CACAGATAATTAGGG	8850
rs2623075	snp	C/T	0.0962929	0.197165	intron-variant	KAT2B	GRCh38.p7	3:20066652	GTGATCCTCCCACCT[C/T]GGCATCCCAAAGTGC	8850
rs2623077	snp	A/G	0.469247	0.120128	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069989	AATTCTCTGTAATGA[A/G]CCATCCACCTCTTCA	8850
rs2623079	snp	C/G	0.472709	0.11358	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069953	TGCAAAGATCTCAGA[C/G]GCCATGTTCTTGAAG	8850
rs2661376	snp	A/G	0.0839998	0.186933	intron-variant	KAT2B	GRCh38.p7	3:20150654	CTTCCTCTGGCCTTC[A/G]TAGAGTTTTTTCAAT	8850
rs2661377	snp	C/T	0.12932	0.218944	intron-variant	KAT2B	GRCh38.p7	3:20145588	AGACAGTGAGGTTAT[C/T]CCTTTAATAAAAAAA	8850
rs2661378	snp	G/T	0.225301	0.248777	intron-variant	KAT2B	GRCh38.p7	3:20143517	ctcagtaataggatt[G/T]ctgtgtggaatggta	8850
rs2661379	snp	A/T	0.0988009	0.199095	intron-variant	KAT2B	GRCh38.p7	3:20139230	TAAGAACACATTTTT[A/T]AAAAAAAAGAAGTCT	8850
rs2686313	snp	A/C	0.266819	0.249434	intron-variant	KAT2B	GRCh38.p7	3:20132845	AAACTATAAATTTGT[A/C]CCCTTCATCCATAAT	8850
rs2686314	snp	A/G	0.142947	0.22592	intron-variant	KAT2B	GRCh38.p7	3:20146582	GGAAGACATAAAAGG[A/G]TAACATTTGCTGCCT	8850
rs2686315	snp	A/G	0.0785177	0.181917	intron-variant	KAT2B	GRCh38.p7	3:20146516	GGCAATAAAGCTTTC[A/G]AAGTTACTGCATTCT	8850
rs2686316	snp	A/T	0.237303	0.249677	intron-variant	KAT2B	GRCh38.p7	3:20145846	CCAAAAGCCTACAGT[A/T]GTTAAAGCTTTACTA	8850
rs2686317	snp	A/G	0.245346	0.249957	intron-variant	KAT2B	GRCh38.p7	3:20145689	ACACAACCATGACAT[A/G]AGCCATCACACTGAC	8850
rs2686318	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20144846	gttgtgccattgcac[C/T]ccagtctgggtgaca	8850
rs2686320	snp	C/T	0.497749	0.0334707	intron-variant	KAT2B	GRCh38.p7	3:20071881	CAGAAGGGAAACCCA[C/T]AGAACCGAAGAAGTT	8850
rs2686321	snp	G/T	0.497749	0.0334707	intron-variant	KAT2B	GRCh38.p7	3:20071810	GGCACACTTGCAGGC[G/T]CCTCCAAGACTTCTG	8850
rs2686322	snp	C/T	0.497749	0.0334707	intron-variant, utr-variant-5-prime	KAT2B	GRCh38.p7	3:20071613	GTAGCCAAGAGTGAA[C/T]ATGATGTAGCCTTCT	8850
rs2686323	snp	A/G	0.499325	0.0183582	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069775	ttgggaggccaaggc[A/G]ggtggatcatgaggt	8850
rs2886463	snp	C/T	0.454664	0.143571	intron-variant	KAT2B	GRCh38.p7	3:20092667	tgatccctttatcat[C/T]atataatgccctttt	8850
rs2929389	snp	A/G	0.468349	0.121752	intron-variant	KAT2B	GRCh38.p7	3:20069144	CTCTCATGTTCATAC[A/G]CAATGAATATGTCAA	8850
rs2929390	snp	A/G	0.468349	0.121752	intron-variant	KAT2B	GRCh38.p7	3:20068969	CCACCCTTATTGTGG[A/G]CCAACCTCTCTTAGT	8850
rs2929391	snp	C/T	0.46974	0.119223	intron-variant	KAT2B	GRCh38.p7	3:20068713	CACTGACTCATTCTT[C/T]CAACAATATTTATTG	8850
rs2929392	snp	C/G	0.46974	0.119223	intron-variant	KAT2B	GRCh38.p7	3:20068579	AATGAGTAAATTATA[C/G]AATATACTGGAGAAT	8850
rs2929393	snp	C/T	0.357451	0.225731	intron-variant	KAT2B	GRCh38.p7	3:20068531	AGAAAGAAAAAAGGA[C/T]GAGTACAGGGAACTT	8850
rs2929394	snp	A/C	0.497984	0.0316851	intron-variant	KAT2B	GRCh38.p7	3:20068409	TAGGTATCTAGTATA[A/C]GGGAAACACAGCTAG	8850
rs2929395	snp	C/T	0.499203	0.0199521	intron-variant	KAT2B	GRCh38.p7	3:20068149	AATTAGTCGGCATGG[C/T]GGTGCACACCTGTAA	8850
rs2929396	snp	A/G	0.469247	0.120128	intron-variant	KAT2B	GRCh38.p7	3:20068141	GGCATGGTGGTGCAC[A/G]CCTGTAATCCCAGCT	8850
rs2929398	snp	C/T	0.18325	0.240924	intron-variant	KAT2B	GRCh38.p7	3:20058562	CTCAGGAGAACAAAA[C/T]TGCCTGGGATTGAGA	8850
rs2929399	snp	C/T	0.095934	0.196885	intron-variant	KAT2B	GRCh38.p7	3:20058559	AGGAGAACAAAACTG[C/T]CTGGGATTGAGATAG	8850
rs2929400	snp	C/T	0.093777	0.195178	intron-variant	KAT2B	GRCh38.p7	3:20055274	AATTTGTTGAGTAAA[C/T]GGAAAAAGTTGACAT	8850
rs2929401	snp	C/T	0.498437	0.0279115	intron-variant	KAT2B	GRCh38.p7	3:20055243	Atatcactgtctcca[C/T]attacagctgcgaaa	8850
rs2929402	snp	A/G	0.488302	0.0755777	intron-variant	KAT2B	GRCh38.p7	3:20054618	ACAAACCTCGCAAAA[A/G]GCTGCACAAGCCAAG	8850
rs2929403	snp	C/T	0.093777	0.195178	intron-variant	KAT2B	GRCh38.p7	3:20054422	CAAAATAAATGCATC[C/T]ATCTCCTTCACATCT	8850
rs2929404	snp	A/G	0.186737	0.241863	intron-variant	KAT2B	GRCh38.p7	3:20053074	ACTTAACTATGAGTA[A/G]GTGTTGTTCCAGCTC	8850
rs2929405	snp	C/T	0.0916144	0.193427	intron-variant	KAT2B	GRCh38.p7	3:20052150	GCTGGCATTTAAGAA[C/T]AGACTGGAATGAGGC	8850
rs2929406	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20052070	GCAGGTAACCACATG[C/T]ACAATTAGATGCTAG	8850
rs2929407	snp	A/T	0.0429648	0.14013	intron-variant	KAT2B	GRCh38.p7	3:20044423	TTTATTTATTTATTT[A/T]TTTTTTTAGGGAGAA	8850
rs2929408	snp	G/T	0.357024	0.225933	intron-variant	KAT2B	GRCh38.p7	3:20041477	AGTAGCGCCCGCCGC[G/T]CTGGGCTGTCACTTT	8850
rs2948078	snp	C/T	0.0448719	0.142907	intron-variant	KAT2B	GRCh38.p7	3:20049856	ATTTGGCACCTTCTA[C/T]AGCCTGAGTAGGTGT	8850
rs2948081	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038055	CACTTTGAATAGGTC[C/T]TGAAACCACGGGCCT	8850
rs2948082	snp	C/T	0.497933	0.032082	intron-variant	KAT2B	GRCh38.p7	3:20054287	GGGTCTGCCACCATA[C/T]GCAGCTAATTTTTGT	8850
rs2948083	snp	A/G	0.167484	0.23599	intron-variant	KAT2B	GRCh38.p7	3:20055481	AATTCCTCTAGATAC[A/G]TGCCCAGGAAATCCT	8850
rs2948084	snp	A/G	0.488666	0.0744214	intron-variant	KAT2B	GRCh38.p7	3:20055975	TGGTAGTTAATTTCT[A/G]TTTATTGCTGAGGAG	8850
rs2948085	snp	C/T	0.188	0.24219	intron-variant	KAT2B	GRCh38.p7	3:20056627	AGGAAAAGAGAAATA[C/T]GGTCAAAGAGAAACT	8850
rs2948086	snp	G/T	0.1652	0.235179	intron-variant	KAT2B	GRCh38.p7	3:20057674	TCCAGGGTACTAGTT[G/T]CTAGGCCCCAGTGTC	8850
rs2948087	snp	C/T	0.17138	0.237316	intron-variant	KAT2B	GRCh38.p7	3:20057723	CCTTTTCAGGGGTAA[C/T]GCATGCTTAGGTTTG	8850
rs2948088	snp	C/T	0.105924	0.204309	intron-variant	KAT2B	GRCh38.p7	3:20058166	ATGGCACTCATAAAT[C/T]AAGGTATTCAGCCAG	8850
rs2948094	snp	C/T	0.497776	0.0332724	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070116	CTACATCAGCATCCC[C/T]ATAGCTACATCCCCC	8850
rs2948095	snp	C/T	0.462253	0.132093	intron-variant	KAT2B	GRCh38.p7	3:20069093	TCTTGTTAATGTATT[C/T]TGTTAGTCTGACTGA	8850
rs2948096	snp	C/T	0.476746	0.10529	intron-variant	KAT2B	GRCh38.p7	3:20068142	CGGCATGGTGGTGCA[C/T]ACCTGTAATCCCAGC	8850
rs2948097	snp	C/T	0.497959	0.0318836	intron-variant	KAT2B	GRCh38.p7	3:20063934	aaaactaggtatctg[C/T]gtgcacaagaatgaa	8850
rs3021408	snp	C/T	0.482842	0.0910197	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072338	ACATTTACAAGACTC[C/T]TCGGCCTAAAAATGG	8850
rs3062235	in-del	-/GAGA			intron-variant	KAT2B	GRCh38.p7	3:20096971	agagagagagagaga[-/GAGA]aagagagtgggggaa	8850
rs3086993	in-del	-/GT	0	0	intron-variant	KAT2B	GRCh38.p7	3:20065571	ATAAGAGCATTGACT[-/GT]TTTTTAAAGGACACA	8850
rs3749180	snp	G/T	0.482893	0.0909217	intron-variant	KAT2B	GRCh38.p7	3:20072497	GTCTCACGCTACAAT[G/T]AACTCGTTATACTTT	8850
rs3749182	snp	A/G	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20072093	GCTACAGCTCACGCA[A/G]CTGACCCACACACTT	8850
rs3749184	snp	A/G	0.138546	0.223781	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153688	ATAGAAAAGTGAGAC[A/G]TCTGCCATTCCCAAC	8850
rs3749185	snp	A/G	0.00318978	0.0398085	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153731	AACTAATATACAACC[A/G]TATAAATGAAGGCCA	8850

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