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
rs10076	snp	C/T	0.167484	0.23599	intron-variant	RCBTB2	GRCh38.p7	13:48505367	ATGTATTTCTAGTGA[C/T]CAATTCAAATTAGTA	1102
rs11861	snp	C/G	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48505141	GCTGCGTGACTAGCA[C/G]TAGGCTGCGTGACTA	1102
rs751334	snp	A/G	0.0387552	0.1337	intron-variant	RCBTB2	GRCh38.p7	13:48506228	AGACCTGACAGGGAC[A/G]GAGGCCAACGCCGGG	1102
rs752663	snp	G/T			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534833	TAGACTAAAAATTTA[G/T]ACTCTGAGAGAGTAT	1102
rs877938	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48512678	TCAATAAGATTATGT[A/T]GACTTCTATAGTAGT	1102
rs877939	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48512677	CAATAAGATTATGTA[G/T]ACTTCTATAGTAGTC	1102
rs943278	snp	A/G	0.499218	0.0197529	intron-variant	RCBTB2	GRCh38.p7	13:48496038	AGACAACGTATAAGC[A/G]AGTATTTATATAATG	1102
rs943279	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48493315	GAGAGAGAGAGAGAG[A/T]GTGTGTGTGTGTGTG	1102
rs943281	snp	C/T	0.0402882	0.136092	intron-variant	RCBTB2	GRCh38.p7	13:48514153	aattgcaagcatcac[C/T]actcttgcactttgg	1102
rs943282	snp	C/T	0.0596104	0.162024	intron-variant	RCBTB2	GRCh38.p7	13:48517696	ATCTTTTCTGAATAA[C/T]CTTCATGGCACTATT	1102
rs943283	snp	C/G	0.499218	0.0197529	intron-variant	RCBTB2	GRCh38.p7	13:48517929	CGTCCAATGACTAGT[C/G]TCCTTAAAAGAAGAC	1102
rs943284	snp	A/G	0.48692	0.0798058	intron-variant	RCBTB2	GRCh38.p7	13:48517982	AGGGAAGAAGGCCAG[A/G]TGACAACAGACACAG	1102
rs977097	snp	C/G	0	0	downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488811	GGAAAGCCCACCCTA[C/G]ACCACAAATAGCTGA	1102
rs2026580	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48495629	TAATATGTATTAAGC[A/C]CCTAAATTAAAGACA	1102
rs2148515	snp	A/G	0.296109	0.245711	intron-variant	RCBTB2	GRCh38.p7	13:48511279	ATAGCAGTTTTCCAT[A/G]TCATTAAAAATTCTT	1102
rs2274400	snp	C/G/T	0.0358264	0.128972	intron-variant	RCBTB2	GRCh38.p7	13:48521886	GCTCCAAGGGCATGA[C/G/T]TTTTTTCTAACCTTG	1102
rs2406934	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48493313	CACACACACACACAC[A/T]CACTCTCTCTCTCTC	1102
rs2897588	snp	C/G	0.499218	0.0197529	intron-variant	RCBTB2	GRCh38.p7	13:48514318	TGGTTCATGTCCCAG[C/G]TGGGATGGAGCAAGA	1102
rs3085589	in-del	-/AC	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48493259	cacacacacacacac[-/AC]tcttctctctctcac	1102
rs3085593	in-del	-/C/CTC/CTCTCTCC/CTCTCTCT/CTCTCTCTCC			intron-variant	RCBTB2	GRCh38.p7	13:48493341	tctctctctctctct[lengthTooLong]tctcttctctctctc	1102
rs3215827	in-del	-/T	0.4021	0.198407	intron-variant	RCBTB2	GRCh38.p7	13:48515485	ACCTAATTTCCATGC[-/T]TTTTTTTTTAACCTT	1102
rs3990837	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48495626	TATGTCTTTAATTTA[A/G]GGGCTTAATACATAT	1102
rs5803440	in-del	-/T			frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512802	TGTTTGTTTGACAGA[-/T]TAGTAGAGATATGAC	1102
rs6561447	snp	C/T	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48508693	acaggcgtgagtgcc[C/T]ggccCATCCATGATT	1102
rs6561448	snp	C/T	0.397452	0.201886	intron-variant	RCBTB2	GRCh38.p7	13:48510190	AATAACCCTATCCTT[C/T]TCAACTGGCAAATTT	1102
rs6561449	snp	C/G	0.0162398	0.0886349	intron-variant	RCBTB2	GRCh38.p7	13:48510222	CATGTAGCTGAGTGA[C/G]CAGCTTTATACCCCA	1102
rs6561450	snp	C/T	0.00713116	0.0592851	intron-variant	RCBTB2	GRCh38.p7	13:48511981	CTGATGTGGCAAACA[C/T]GGTTTTTAAACAAGA	1102
rs6561451	snp	C/G	0.00707995	0.0590749	intron-variant	RCBTB2	GRCh38.p7	13:48512206	TCAGTAAATGAAACA[C/G]ATTAATTTATAAACT	1102
rs6561452	snp	C/G	0.0295753	0.118402	intron-variant	RCBTB2	GRCh38.p7	13:48512462	TTTTCCAGCATTTGG[C/G]GATTTTTCTTATTGC	1102
rs6561453	snp	A/G	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48512463	TTTCCAGCATTTGGG[A/G]ATTTTTCTTATTGCA	1102
rs6561454	snp	A/G	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48512505	TACTACAGCAACAGA[A/G]AAGGAACAATACCTC	1102
rs6561455	snp	A/G	0.0729998	0.176553	intron-variant	RCBTB2	GRCh38.p7	13:48518349	AAGACCTTGCCCTAA[A/G]AAGGACACCTTCTGT	1102
rs6561456	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48518472	GCAAAAAAAAAAAAa[A/T]atatatatatatata	1102
rs6561457	snp	C/G	0.397452	0.201886	intron-variant	RCBTB2	GRCh38.p7	13:48523751	CAGAAGGGAAATCTT[C/G]CTAATGTGCTAAAAT	1102
rs7316991	snp	A/T	0.116138	0.211142	intron-variant	RCBTB2	GRCh38.p7	13:48491429	TAAGCCCTCAGTGAT[A/T]AACAGGGAAAATTCA	1102
rs7317090	snp	A/G	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48513145	ATAAGTTTTTAATAA[A/G]GAGCAGAGAAAAGGC	1102
rs7319069	snp	C/T	0.135825	0.222405	intron-variant	RCBTB2	GRCh38.p7	13:48491688	GTGTCTGGAGTTAGG[C/T]GGCTGGGCAGTTTGA	1102
rs7319392	snp	A/T	0.444444	0.157135	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499144	cacacacacacacac[A/T]ctctctctctctctc	1102
rs7321483	snp	C/T	0.00723129	0.0596938	intron-variant	RCBTB2	GRCh38.p7	13:48496164	ATTTCTCCAGGAGGC[C/T]GGCAGCTGGAAGCAA	1102
rs7322110	snp	A/G	0.151001	0.229563	intron-variant	RCBTB2	GRCh38.p7	13:48513402	aaatataaccttata[A/G]tcaccccccaaaagg	1102
rs7322265	snp	C/T	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48513408	aaccttataatcacc[C/T]cccaaaaggccctca	1102
rs7322788	snp	C/T	0.0349115	0.127424	intron-variant	RCBTB2	GRCh38.p7	13:48526175	CCTTTACCAAGGACA[C/T]GGAAATTCAATAAAC	1102
rs7322855	snp	C/T	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48513735	TTCAAATAAtaaata[C/T]agctgtcttataatt	1102
rs7323517	snp	C/T	0.116488	0.211364	intron-variant	RCBTB2	GRCh38.p7	13:48491188	TATGAACATTACACA[C/T]GATAGTCTTTTCTTC	1102
rs7324752	snp	C/T	0.116138	0.211142	intron-variant	RCBTB2	GRCh38.p7	13:48491123	CTCTCCAAGCTACTG[C/T]AGGTAATTTATAAAA	1102
rs7325162	snp	A/G	0.030278	0.119257	intron-variant	RCBTB2	GRCh38.p7	13:48531630	agagcaataaggcct[A/G]agtggtggaagtggg	1102
rs7325962	snp	C/T	0.406986	0.194565	intron-variant	RCBTB2	GRCh38.p7	13:48492967	attcaaaaccaaatt[C/T]ctgatatttccccca	1102
rs7326934	snp	C/G	0.364193	0.222396	intron-variant	RCBTB2	GRCh38.p7	13:48496376	GCATCCTGATTTACA[C/G]TTGCTCACTCAGCCA	1102
rs7330657	snp	A/G	0.0263992	0.111815	intron-variant	RCBTB2	GRCh38.p7	13:48523659	GAAGAAAGAGGGAGA[A/G]AAGAGAAAAAAGAAG	1102
rs7331860	snp	C/T	0.0162398	0.0886349	intron-variant	RCBTB2	GRCh38.p7	13:48532814	CCCCGGAACCTAGCT[C/T]TTAACTCCCGCCAGC	1102
rs7332828	snp	A/G	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48511713	GTTTTTAATACATTG[A/G]TATCTTTGCCAGCGA	1102
rs7332852	snp	C/T	0.0387552	0.1337	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501298	CTGTGCTAGCCTCAC[C/T]ATAGACCTTTTTGGT	1102
rs7333474	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48518474	AAAAAAAAAAAAAAA[A/T]ATATATATATATATA	1102
rs7334590	snp	G/T	0.00716407	0.0594198	synonymous-codon, missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511772	ACAGTGGACGTACCC[G/T]CTGGACACGGATGCC	1102
rs7981750	snp	C/T	0.143284	0.226079	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489785	CAGCCAGCTGAATAA[C/T]GGAACATTTGGGCCA	1102
rs7981773	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48519914	ctgagcatccctaat[C/T]caaaaatctgaatcc	1102
rs7984198	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48508010	TTCTGGGAAAGATTT[A/T]AAAAGGTTTCCCTTG	1102
rs7984309	snp	C/T	0.0825414	0.185628	intron-variant	RCBTB2	GRCh38.p7	13:48516516	tgtcttctccctatg[C/T]ctgttcacatcatct	1102
rs7984753	snp	G/T	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48508311	GAATACGCCCGTGAT[G/T]GAGTGCCTGGTTGAA	1102
rs7987935	snp	A/G	0.140919	0.224948	intron-variant	RCBTB2	GRCh38.p7	13:48529950	GACTGGAGTGCAATG[A/G]TGTGATCATGACTCA	1102
rs7987986	snp	C/T	0.0240643	0.107019	intron-variant	RCBTB2	GRCh38.p7	13:48530108	tttgccatgttgtcc[C/T]ggctggtctctaact	1102
rs7988584	snp	A/G/T	0.00874735	0.0655527	intron-variant	RCBTB2	GRCh38.p7	13:48508647	gacctcaggtgatcc[A/G/T]cccgccttggcctcc	1102
rs7988909	snp	C/T	0.00678886	0.0578648	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501702	AATATAATTGTTGAA[C/T]GAATTACTTTTCTCA	1102
rs7989808	snp	C/G	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48502197	TAAAATTAAAAAGCA[C/G]TCAAATAAGGATAgg	1102
rs7990414	snp	C/T	0.039522	0.134904	intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48517503	AAGTCCTCAAACTTT[C/T]AAGTTTCCTTCTGAT	1102
rs7995216	snp	A/G	0.197703	0.244469	intron-variant	RCBTB2	GRCh38.p7	13:48524200	GTTTGTGCACTACAC[A/G]TGGAGATTACCTTAC	1102
rs7996186	snp	C/G	0.0644693	0.167566	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533368	TCACCCCCACCTTCT[C/G]CAGGGTTATGTTCTC	1102
rs7997110	snp	C/T	0.228494	0.249073	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533105	GGCCCGGCGCCGCGA[C/T]GAGTTGGCGCCTCCC	1102
rs8001241	snp	A/G	0.397633	0.201754	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533517	GCCCCTCTATCTGGG[A/G]GCTCCGATCACTTCA	1102
rs8002023	snp	A/G	0.0162398	0.0886349	intron-variant	RCBTB2	GRCh38.p7	13:48519549	CTGGGATTCCAATGC[A/G]TGTGTTTTCTTTAAT	1102
rs9316381	snp	A/G	0.327445	0.237702	intron-variant	RCBTB2	GRCh38.p7	13:48494283	ATTTGCCTGGCTCAA[A/G]TAAGCAAGAAATGGG	1102
rs9316382	snp	A/G	0.499218	0.0197529	intron-variant	RCBTB2	GRCh38.p7	13:48495279	ATGGTGGGATTGTGG[A/G]TGATTTTTATTTTCT	1102
rs9316383	in-del	-/AAGGA	0.364193	0.222396	intron-variant	RCBTB2	GRCh38.p7	13:48495987	AGAAGCCATAAAGGA[-/AAGGA]TTTATAGCTCTGATT	1102
rs9316384	snp	G/T	0.222035	0.248431	intron-variant	RCBTB2	GRCh38.p7	13:48500233	TCATATTGGATTAGG[G/T]CCCACCCTAGTGACC	1102
rs9316385	snp	C/T	0.397633	0.201754	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503605	GCCAAGATCCAAGAT[C/T]GTGCCACTGCACTCT	1102
rs9316386	snp	A/G	0.315273	0.241329	intron-variant	RCBTB2	GRCh38.p7	13:48505515	TTGTTGAAAAGAATG[A/G]TGCTGATTGAGAAGC	1102
rs9316387	snp	G/T	0.222333	0.248464	intron-variant	RCBTB2	GRCh38.p7	13:48514287	TCCCTTTGTCCAGCA[G/T]CTCTGCCATAGACAC	1102
rs9316388	snp	A/G	0.32768	0.237625	intron-variant	RCBTB2	GRCh38.p7	13:48515087	TATGTTTTGGATACC[A/G]TAAAACATGAATGTA	1102
rs9316389	snp	A/G	0.0948562	0.196037	intron-variant	RCBTB2	GRCh38.p7	13:48517011	CCAGACCACATTCCC[A/G]GTAAGGTTGATTTAA	1102
rs9316390	snp	G/T	0.0955749	0.196603	intron-variant	RCBTB2	GRCh38.p7	13:48517783	gccattcaacccaCT[G/T]CAGCTCCTCTCTGGG	1102
rs9316391	snp	A/G	0.095934	0.196885	intron-variant	RCBTB2	GRCh38.p7	13:48517978	gtctgttgtcatctg[A/G]ccttcttccctgtgc	1102
rs9316392	snp	A/G	0.166832	0.235761	intron-variant	RCBTB2	GRCh38.p7	13:48519447	ATCATTTGTAGACAG[A/G]TATGTAAGAGCTGGC	1102
rs9316393	snp	C/T	0.328148	0.237472	intron-variant	RCBTB2	GRCh38.p7	13:48520790	TTAAATATACTGTAT[C/T]TTAAATTGAATTGCA	1102
rs9316394	snp	C/T	0.499218	0.0197529	intron-variant	RCBTB2	GRCh38.p7	13:48526428	GTAGTCCCAGCTACT[C/T]GGGAGGCTAAGATAG	1102
rs9316395	snp	A/T	0.49925	0.0193545	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533826	TGAGTGGGTTTTGGT[A/T]AAATGCTCAACAATT	1102
rs9316396	snp	A/G	0.335559	0.234904	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533874	CCTGTGAAGTAAGCT[A/G]CTTGCTTTTATACTG	1102
rs9331951	snp	C/T	0.0349115	0.127424	intron-variant	RCBTB2	GRCh38.p7	13:48524935	TTACATTTTATAACT[C/T]TAGTATTTTTATAAT	1102
rs9331952	snp	A/G	0.0127383	0.0787839	intron-variant	RCBTB2	GRCh38.p7	13:48524640	CAAAAGTTTTTGGAG[A/G]GAATGCTCCCAGCCA	1102
rs9331953	snp	C/G	0.00676609	0.0577691	intron-variant	RCBTB2	GRCh38.p7	13:48524442	TGAATAAAATGGAGG[C/G]AATGATTAacctgtt	1102
rs9331954	snp	C/T	0.0244538	0.107838	intron-variant	RCBTB2	GRCh38.p7	13:48524431	GAGGCAATGATTAac[C/T]tgtttcatttggata	1102
rs9331955	snp	A/T	0.00478085	0.0486577	intron-variant	RCBTB2	GRCh38.p7	13:48524144	TTTTCTTTATTATGT[A/T]TGCATCACATTGAAA	1102
rs9331956	snp	A/G	0.0341408	0.126114	intron-variant	RCBTB2	GRCh38.p7	13:48523968	CTTACATTTCATTCA[A/G]TTTGAATCCTGCATG	1102
rs9331957	snp	C/T	0.039522	0.134904	intron-variant	RCBTB2	GRCh38.p7	13:48523918	AATTTCCATGACATA[C/T]ATACAATTATGTCTT	1102
rs9331958	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48523777	CAAAAGCCCAGGATC[A/G]GTTTTTCATGATTTT	1102
rs9331959	snp	C/G	0.0644693	0.167566	intron-variant	RCBTB2	GRCh38.p7	13:48523651	TTCTCTTCTCTCCCT[C/G]TTTCTTCTCCTCTCC	1102
rs9331960	snp	C/T	0.00716266	0.059414	intron-variant	RCBTB2	GRCh38.p7	13:48523617	tattttttattcCAG[C/T]AAACTTGGGGCAAAT	1102
rs9331961	snp	C/T	0.00478085	0.0486577	intron-variant	RCBTB2	GRCh38.p7	13:48523606	cCAGTAAACTTGGGG[C/T]AAATATGGAAAAAGT	1102
rs9331962	snp	A/G	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48523582	AAAAAGTGTTTCCTG[A/G]TAGGGTGAGGCAGAA	1102
rs9331963	snp	C/T	0.0228947	0.104514	intron-variant	RCBTB2	GRCh38.p7	13:48523451	TGTGGGTTATAGCAA[C/T]GAAGGAATCGTCTGC	1102
rs9331964	snp	G/T	0.00398564	0.0444627	intron-variant	RCBTB2	GRCh38.p7	13:48523062	ATATCTTTTTTACTT[G/T]TTTCCAAATGTTAGA	1102

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