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
rs473654	snp	C/T	0.26818	0.249338	intron-variant	SPSB1	GRCh38.p7	1:9351608	CTGGACTCGCCACCT[C/T]CCCTGGAACTGCAGC	80176
rs478103	snp	C/T	0.219648	0.248151	intron-variant	SPSB1	GRCh38.p7	1:9342344	GACAAGTCCAGAAAC[C/T]GTGTGCATCAGCCTG	80176
rs478552	snp	A/G	0.330249	0.23677	intron-variant	SPSB1	GRCh38.p7	1:9298420	aacgaatgaatgaat[A/G]agtgaacgaatgaat	80176
rs479043	snp	G/T	0.459347	0.136653	intron-variant	SPSB1	GRCh38.p7	1:9342461	GATCCCAGTGGCTTG[G/T]CAATTCGCTGATAGC	80176
rs482215	snp	C/T	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9347904	TGGGGAAAGGACACT[C/T]CTACACACTGTGGGT	80176
rs483823	snp	C/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9353154	AGAGCTGCATGGAGC[C/G]GGGGTGCAGAGTACC	80176
rs483934	snp	C/T	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9347744	ACCAAACCCTATAGG[C/T]CTGCACAGGGACATG	80176
rs483936	snp	C/G	0.453939	0.144598	intron-variant	SPSB1	GRCh38.p7	1:9347741	AAACCCTATAGGCCT[C/G]CACAGGGACATGAGG	80176
rs504357	snp	A/G	0.348354	0.22984	intron-variant	SPSB1	GRCh38.p7	1:9340093	CACAGACCATCACCC[A/G]GGAGCTTGCTGGAAA	80176
rs504358	snp	C/G	0.476052	0.106772	intron-variant	SPSB1	GRCh38.p7	1:9340096	CCAGCAAGCTCCTGG[C/G]TGATGGTCTGTGGGC	80176
rs507656	snp	C/G	0.498673	0.0257246	intron-variant	SPSB1	GRCh38.p7	1:9318653	AGGCACCAGCCACAC[C/G]GTCTGGCTTTGGTCA	80176
rs510666	snp	A/G	0.0287284	0.116357	intron-variant	SPSB1	GRCh38.p7	1:9343616	AGAAATGAAAATGTC[A/G]CTGTGTTTAGAGTGA	80176
rs513170	snp	C/T	0.0228947	0.104514	intron-variant	SPSB1	GRCh38.p7	1:9343872	catgaacccaggagg[C/T]ggagctttcagtgag	80176
rs515748	snp	A/C	0	0	intron-variant	SPSB1	GRCh38.p7	1:9361197	ttagagatggggtat[A/C]actatgttgcctagg	80176
rs522526	snp	C/T	0.457853	0.138915	intron-variant	SPSB1	GRCh38.p7	1:9315146	GGCTGAGAAGCTCAG[C/T]GGGGCTGGGACAAGA	80176
rs525476	snp	A/G	0.481932	0.0933148	intron-variant	SPSB1	GRCh38.p7	1:9315527	TCACATTCACATTCA[A/G]CTCCCACCCCGTCAT	80176
rs531796	snp	A/G	0.426813	0.17674	intron-variant	SPSB1	GRCh38.p7	1:9306366	CCTCCTCCAGGCTGG[A/G]CATCACAAAGGAAAA	80176
rs536073	snp	A/C	0.445328	0.156035	intron-variant	SPSB1	GRCh38.p7	1:9319471	GCCTCGGAGCCTCTC[A/C]TCCCACCCCTGTACT	80176
rs536211	snp	C/G	0.423257	0.180228	intron-variant	SPSB1	GRCh38.p7	1:9349407	ACTCACCTACCCCCA[C/G]TCCTGGCCCGGCACA	80176
rs543576	snp	C/T	0.375598	0.21616	intron-variant	SPSB1	GRCh38.p7	1:9365216	acagtggcacaatca[C/T]agcttactgcagcct	80176
rs544264	snp	C/T	0.219947	0.248187	intron-variant	SPSB1	GRCh38.p7	1:9344958	GTGCCAAGGCCTGAA[C/T]GGGAGCCAGTGACAC	80176
rs547506	snp	C/T	0.43221	0.171171	intron-variant	SPSB1	GRCh38.p7	1:9301947	ttggcagaagcactg[C/T]gtgcagggaagacga	80176
rs552230	snp	G/T	0.430136	0.173352	intron-variant	SPSB1	GRCh38.p7	1:9362816	CAGGCGCTATTTCTG[G/T]GAGCAGAAGCCTGAG	80176
rs553161	snp	A/G	0.270892	0.249126	intron-variant	SPSB1	GRCh38.p7	1:9362918	GCTATGCCCATCCCC[A/G]GGAAGCTTAGGCGCT	80176
rs554020	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9302639	agtctttggcctggg[A/C]ctgggaatgaccacg	80176
rs557573	snp	C/T	0.234692	0.249531	intron-variant	SPSB1	GRCh38.p7	1:9316737	TCCGGGGCGGTCTCC[C/T]CTGGAGAAGCAGCCG	80176
rs563317	snp	C/G	0.493477	0.0567349	intron-variant	SPSB1	GRCh38.p7	1:9297889	agacagatctttcac[C/G]catacgttgagaaat	80176
rs563347	snp	A/G	0.166832	0.235761	intron-variant	SPSB1	GRCh38.p7	1:9297901	cacgcatacgttgag[A/G]aatagatttgtgagg	80176
rs564709	snp	C/T	0.252421	0.249988	intron-variant	SPSB1	GRCh38.p7	1:9322226	AGACGATGCTGGTAC[C/T]CTACTCAGCCTGATG	80176
rs577685	snp	A/G	0.499995	0.00159744	intron-variant	SPSB1	GRCh38.p7	1:9302900	atcccctagggaccc[A/G]ctagcgaaattgttg	80176
rs581587	snp	A/G	0.34146	0.23267	intron-variant	SPSB1	GRCh38.p7	1:9306793	CAATCCCCATTACCT[A/G]GGACCACTTCTGACT	80176
rs602386	snp	C/G	0.391583	0.206044	intron-variant	SPSB1	GRCh38.p7	1:9345864	TATTTTTATATCCCT[C/G]CTTGAGGGGTCCCTC	80176
rs603590	snp	A/G	0.495671	0.0463237	intron-variant	SPSB1	GRCh38.p7	1:9318805	TGTCCCCCACTATAT[A/G]CAGTGAGTCCTTGGA	80176
rs617018	snp	C/T	0.445592	0.155704	intron-variant	SPSB1	GRCh38.p7	1:9318043	GGAAAGGGGAATGAG[C/T]GCAGCTGCTTCCTCT	80176
rs617901	snp	C/T	0.0248432	0.108648	intron-variant	SPSB1	GRCh38.p7	1:9317880	AAACTCCCACCAAAG[C/T]GACCCGCCAATCTGC	80176
rs618432	snp	A/G	0.0547245	0.156101	intron-variant	SPSB1	GRCh38.p7	1:9351159	aaatcaatgggcatg[A/G]atgtgtttcaataaa	80176
rs619224	snp	A/G	0.00597247	0.0543191	intron-variant	SPSB1	GRCh38.p7	1:9351037	ATTCCTGGACATGGC[A/G]CTCAGGACAGGGGGT	80176
rs619282	snp	A/G	0.276267	0.248616	intron-variant	SPSB1	GRCh38.p7	1:9351001	CCACCCACAGGTACC[A/G]AGTAACATTCACAGG	80176
rs619928	snp	C/T	0.484701	0.0861117	intron-variant	SPSB1	GRCh38.p7	1:9298622	gtaaccagttatccc[C/T]gaacaatctaattat	80176
rs621655	snp	A/G	0.357664	0.225629	intron-variant	SPSB1	GRCh38.p7	1:9365968	TGCGCGGCCCTGCTC[A/G]CCCGCTTCGCCAGAG	80176
rs621846	snp	A/G	0.493748	0.0555599	intron-variant	SPSB1	GRCh38.p7	1:9298184	aagtaagaatttcac[A/G]ggtttcctgtctatt	80176
rs622662	snp	C/G	0.493477	0.0567349	intron-variant	SPSB1	GRCh38.p7	1:9298026	tactgccacttggcc[C/G]ctgcactccaaatgc	80176
rs624927	snp	A/G	0.460813	0.134379	intron-variant	SPSB1	GRCh38.p7	1:9337484	GTTTGGGGACAGGAA[A/G]CCCTCTTTGGGGGGA	80176
rs628739	snp	C/T	0.453575	0.145111	intron-variant	SPSB1	GRCh38.p7	1:9311150	AAAAACCCTTTATCC[C/T]GCGCTGTCTAGACAC	80176
rs629524	snp	A/C	0.499954	0.00479211	intron-variant	SPSB1	GRCh38.p7	1:9311040	CACACTGACCAGCTC[A/C]AAATTGGCCCGATAG	80176
rs630075	snp	C/T	0.499961	0.0043928	intron-variant	SPSB1	GRCh38.p7	1:9310852	CTTCCCCAAGCTTCA[C/T]AAATGCAAGGCAACC	80176
rs631824	snp	C/T	0.0248432	0.108648	intron-variant	SPSB1	GRCh38.p7	1:9343865	ccaggaggcggagct[C/T]tcagtgagccgagat	80176
rs643762	snp	A/T	0.376989	0.215346	intron-variant	SPSB1	GRCh38.p7	1:9343512	GAGCCCAAATGTCCA[A/T]CAATGGATGCATGGA	80176
rs644728	snp	C/T	0.219947	0.248187	intron-variant	SPSB1	GRCh38.p7	1:9343244	GGAAGTGACAGAGGT[C/T]TCTTTTAGGGGTGAT	80176
rs658738	snp	G/T	0.459118	0.137002	intron-variant	SPSB1	GRCh38.p7	1:9342459	AGGATCCCAGTGGCT[G/T]GTCAATTCGCTGATA	80176
rs662553	snp	A/G	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9348236	TTAAAAAAAGTTGCc[A/G]cggtggctcacgcct	80176
rs663419	snp	A/G	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9348026	acccaggaggcggag[A/G]ttgcagtgagccgag	80176
rs664347	snp	A/G	0.282895	0.247826	intron-variant	SPSB1	GRCh38.p7	1:9347797	TGTGCAAAACGCCCA[A/G]CAATCACCCAGCAAC	80176
rs664623	snp	C/T	0.253824	0.249971	intron-variant	SPSB1	GRCh38.p7	1:9322298	GAACCTCAGTTTCCC[C/T]ACCTGCAAACCGAGG	80176
rs664730	snp	A/G	0.00914312	0.0669923	intron-variant	SPSB1	GRCh38.p7	1:9347724	GTCCCCAGCATCTTC[A/G]TCCTCATGTCCCTGT	80176
rs672453	snp	C/T	0.496937	0.0390173	intron-variant	SPSB1	GRCh38.p7	1:9301724	gagtggcagtccatg[C/T]tgctgagcccatgca	80176
rs732590	snp	C/T	0.439363	0.163222	intron-variant	SPSB1	GRCh38.p7	1:9329172	CTGCAGTGCCCCTCA[C/T]ACTGCTTCATACAAC	80176
rs732591	snp	A/G	0.409382	0.192607	intron-variant	SPSB1	GRCh38.p7	1:9329159	CACACTGCTTCATAC[A/G]ACTGCCCTTAGGTGT	80176
rs732592	snp	A/G	0.402454	0.198136	intron-variant	SPSB1	GRCh38.p7	1:9329112	TGGGAGGCTGTCCCC[A/G]CCACCCTGTCCCCCA	80176
rs733096	snp	C/T	0.179744	0.239925	intron-variant	SPSB1	GRCh38.p7	1:9341235	TGGTGGGGAGTGGTG[C/T]GTGTACCGTGCCTCT	80176
rs733892	snp	C/T	0.210605	0.246877	intron-variant	SPSB1	GRCh38.p7	1:9354338	AGGAGCCTGTGGGGG[C/T]GCCTGGGCGGGAGGC	80176
rs733893	snp	C/T	0.385359	0.210185	intron-variant	SPSB1	GRCh38.p7	1:9354950	GGGAGGAAAGTCCGA[C/T]GCTAGGATGCCTCGT	80176
rs909511	snp	C/T	0.401392	0.198948	intron-variant	SPSB1	GRCh38.p7	1:9329403	TGACCTACCCACCAC[C/T]GGGTGTCACCTCCCC	80176
rs926247	snp	A/G	0.4087	0.193169	intron-variant	SPSB1	GRCh38.p7	1:9333949	TACTGGGACAAAAGC[A/G]AAAAAATGAGAAGGA	80176
rs926248	snp	C/T	0.164873	0.23506	intron-variant	SPSB1	GRCh38.p7	1:9317937	TGGCACACAGGGGCC[C/T]TTAACAAACTCGCGG	80176
rs926249	snp	A/G	0.188316	0.242271	intron-variant	SPSB1	GRCh38.p7	1:9317805	GGAAATCACCTACAT[A/G]AGGCTCTGAAACTGT	80176
rs926250	snp	C/T	0.460589	0.13473	intron-variant	SPSB1	GRCh38.p7	1:9314316	TTGTATATTTAGGAG[C/T]GGGAGGGAGGAAGGA	80176
rs1005246	snp	A/G	0.211212	0.246973	intron-variant	SPSB1	GRCh38.p7	1:9364340	CAGCCAGGCCAGACC[A/G]CAGGCTGCGATAAGC	80176
rs1008678	snp	C/T	0.0146672	0.084371	intron-variant	SPSB1	GRCh38.p7	1:9321152	TTTCCAGCTTTGTGT[C/T]TTGGGGGGATTTTTT	80176
rs1008679	snp	C/T	0.208779	0.246578	intron-variant	SPSB1	GRCh38.p7	1:9321027	CCAGCCAGAATCCCC[C/T]GCACAGCAACTCCCA	80176
rs1033377	snp	C/T	0.46137	0.133501	intron-variant	SPSB1	GRCh38.p7	1:9319302	GCACACATGTCCACA[C/T]GCTGACCCGCAGCCC	80176
rs1294020	snp	A/G	0.4087	0.193169	intron-variant	SPSB1	GRCh38.p7	1:9335202	ACAACATTCTTTTGA[A/G]GCACAAAGATACCTT	80176
rs1294021	snp	G/T	0.0236746	0.106192	intron-variant	SPSB1	GRCh38.p7	1:9333929	AATGAGAAGGAATGT[G/T]GCGGAGCATCCCTGG	80176
rs1294022	snp	C/G	0.412416	0.190055	intron-variant	SPSB1	GRCh38.p7	1:9333023	GGGCAGAAGCTCAGT[C/G]AGCACTTGCTGGTGG	80176
rs1294023	snp	C/T	0.329783	0.236927	intron-variant	SPSB1	GRCh38.p7	1:9332029	TCTGTAATTCAAACA[C/T]GTACAAAAGAGTCAC	80176
rs1294024	snp	A/G	0.436408	0.16659	intron-variant	SPSB1	GRCh38.p7	1:9354433	AGAGAGGCCAAGGAG[A/G]GCAGCCTGGTTTGGG	80176
rs1294025	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9353791	agctgggattacagg[C/T]gcccaccaccacgcc	80176
rs1294027	snp	C/T	0.265453	0.249522	intron-variant	SPSB1	GRCh38.p7	1:9352255	AAGGACGGCTTCACC[C/T]TGACGTGGGACATCC	80176
rs1294028	snp	C/T	0.43555	0.167544	intron-variant	SPSB1	GRCh38.p7	1:9304575	ACTAGTTACCGAAGC[C/T]TACCCATGCCACCTT	80176
rs1294030	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9301127	cagccaaatcatcag[A/G]cacagcccatggatc	80176
rs1294031	snp	A/G	0.301429	0.244653	intron-variant	SPSB1	GRCh38.p7	1:9301115	caggcacagcccatg[A/G]atcagtatataatca	80176
rs1294032	snp	A/G	0.499741	0.0113788	intron-variant	SPSB1	GRCh38.p7	1:9300377	gcaggttgcacagca[A/G]cctggacctgttgca	80176
rs1294033	snp	C/T	0.0402882	0.136092	intron-variant	SPSB1	GRCh38.p7	1:9300240	caggcccacgaggca[C/T]tgtgcctctttcttg	80176
rs1294034	snp	A/T	0.16911	0.236552	intron-variant	SPSB1	GRCh38.p7	1:9300177	tcaccttagagggga[A/T]accttcacaggcctg	80176
rs1294035	snp	C/T	0.16846	0.236329	intron-variant	SPSB1	GRCh38.p7	1:9300149	ctgacactactggac[C/T]ccgagaaatttcact	80176
rs1294036	snp	A/G	0.163236	0.234461	intron-variant	SPSB1	GRCh38.p7	1:9299628	gctgggtgtggtggc[A/G]catgcctgtaatccc	80176
rs1294037	snp	C/T	0.448708	0.151707	intron-variant	SPSB1	GRCh38.p7	1:9299573	agaattgcttgaacc[C/T]gggaggcggaggttg	80176
rs1294038	snp	A/C	0.078151	0.181571	intron-variant	SPSB1	GRCh38.p7	1:9309146	GCCCACCGACGACCC[A/C]TGGGCCTGGCATTTG	80176
rs1294039	snp	C/T	0.0260105	0.111035	intron-variant	SPSB1	GRCh38.p7	1:9308979	CTGCCAGGGGCTGGG[C/T]GGGCACCAGGCCTGC	80176
rs1294040	snp	C/T	0.45946	0.136478	intron-variant	SPSB1	GRCh38.p7	1:9308150	CCCCTTTGGGCCTGA[C/T]ATGTCTTGGAAAACA	80176
rs1294041	snp	C/T	0.155325	0.23138	intron-variant	SPSB1	GRCh38.p7	1:9307289	accaaatgccactga[C/T]ctgttcactttaaaa	80176
rs1294042	snp	A/G	0.486	0.0824865	intron-variant	SPSB1	GRCh38.p7	1:9306426	CTATAGACAGACCCC[A/G]GTCCATGCACCTCCC	80176
rs1294044	snp	C/T	0.497502	0.035255	intron-variant	SPSB1	GRCh38.p7	1:9306340	GAAAACTGGTTATCC[C/T]TCCCACTCCAGCTCT	80176
rs1294045	snp	G/T	0.459233	0.136827	intron-variant	SPSB1	GRCh38.p7	1:9319682	GGCCGGGCCAGACGA[G/T]CAGGCTTGGCCTCCC	80176
rs1294046	snp	C/T	0.499946	0.00519141	intron-variant	SPSB1	GRCh38.p7	1:9319634	AGCCGGAACGGAATA[C/T]CAGCCCGGTACGGAA	80176
rs1294047	snp	A/G	0.498503	0.0273153	intron-variant	SPSB1	GRCh38.p7	1:9319206	ACCTCCTCTTTTGTT[A/G]TTGTTACTGTTGttt	80176
rs1294048	snp	C/T	0.495671	0.0463237	intron-variant	SPSB1	GRCh38.p7	1:9318913	tgtgagccactgcgc[C/T]cggccCTACCACGTC	80176
rs1294049	snp	C/T	0.499839	0.00898417	intron-variant	SPSB1	GRCh38.p7	1:9318876	ACTCACTGCAGGACA[C/T]CGCAGGCTGGACTCC	80176
rs1294050	snp	G/T	0.471388	0.116136	intron-variant	SPSB1	GRCh38.p7	1:9314417	GGGAAGATGGGCACC[G/T]GGCTGCCCACTTGTG	80176
rs1294051	snp	C/G	0.231111	0.249285	intron-variant	SPSB1	GRCh38.p7	1:9313592	TCTCCCCCAGCAGCC[C/G]GGGCCCACCCCTCCC	80176

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