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
rs11333	snp	A/T	0	0	utr-variant-3-prime, nc-transcript-variant	RNF138	GRCh38.p7	18:32130552	TGTTCTTCTAGTTAT[A/T]TTAAAGAAAGCATAA	51444
rs593234	snp	C/T	0.24019	0.249807	intron-variant	RNF138	GRCh38.p7	18:32099959	TCACTAGAGCTGCAA[C/T]TATTCTTGTGTGATG	51444
rs684359	snp	A/G	0.0562307	0.157967	intron-variant	RNF138	GRCh38.p7	18:32129018	GTGTGTGTAATGTGT[A/G]TCAAGATGTGTAATG	51444
rs684693	snp	C/T	0.0577344	0.159793	intron-variant	RNF138	GRCh38.p7	18:32101283	tacagtgagccaaga[C/T]tgcgtgtgccactgc	51444
rs865450	snp	C/T	0.0391387	0.134304	intron-variant	RNF138	GRCh38.p7	18:32097557	ggtgggatcttggtt[C/T]actgtaacctccacc	51444
rs1054667	snp	A/C	0.490007	0.0699769	utr-variant-3-prime, nc-transcript-variant	RNF138	GRCh38.p7	18:32131298	AAATGATTGTTTAAA[A/C]TTTCCCCTCTTTTTG	51444
rs1059390	snp	A/T	0	0	synonymous-codon, nc-transcript-variant	RNF138	GRCh38.p7	18:32129169	TGCTGTTGAAGAATC[A/T]TTTCAAGTAAACATC	51444
rs1114052	snp	A/C	0	0	intron-variant	RNF138	GRCh38.p7	18:32126996	TTGAGTTTACTCTCC[A/C]CCTCCTGTACTATAG	51444
rs1814795	snp	C/T	0.446771	0.154211	intron-variant	RNF138	GRCh38.p7	18:32122606	AGGTGGGCGGATCAC[C/T]TGAGCTCAGGAGTTC	51444
rs2010813	snp	A/G	0.496681	0.0405994	intron-variant	RNF138	GRCh38.p7	18:32128336	tgaggtcagcagttc[A/G]agaccagcctggcca	51444
rs2048245	snp	C/T	0.489434	0.0719116	intron-variant	RNF138	GRCh38.p7	18:32111644	TGTACATATGAGTAG[C/T]CTAACTTATTTAATA	51444
rs2136405	snp	A/T			intron-variant	RNF138	GRCh38.p7	18:32096920	ACAAAGCAAGACCCA[A/T]CTCTACAAAAAAATT	51444
rs3760567	snp	A/G	0.0283406	0.115616	upstream-variant-2KB, utr-variant-3-prime	RNF138, RNF125	GRCh38.p7	18:32090021	gaggccaaggtgggc[A/G]gatcgctggaggcca	51444
rs3760568	snp	A/G	0.424193	0.179323	upstream-variant-2KB	RNF138	GRCh38.p7	18:32091758	GAAAACTTCCTGAAA[A/G]GCCCAATGTATTTGA	51444
rs3834614	in-del	-/TTAT			upstream-variant-2KB	RNF138	GRCh38.p7	18:32091671	GTAACAAATATTTGT[-/TTAT]AACACATCTTGACAA	51444
rs3962083	snp	C/T	0	0	intron-variant	RNF138	GRCh38.p7	18:32127621	AAATTCAAATATATG[C/T]AAAATTTAGGTGCGC	51444
rs3980843	snp	A/G	0	0	intron-variant	RNF138	GRCh38.p7	18:32127312	TGTAAAAATGAATTC[A/G]TAAAGCAAAATGGAT	51444
rs3980844	in-del	-/TT			utr-variant-3-prime, nc-transcript-variant	RNF138	GRCh38.p7	18:32131379	TATGGGGAAAAGTTT[-/TT]ATTTTTAATATTACT	51444
rs4239373	snp	C/T	0.440884	0.161442	intron-variant	RNF138	GRCh38.p7	18:32122124	cacccgcctcagcct[C/T]gcaaagtgctgggat	51444
rs4239374	snp	C/T	0.197082	0.244335	intron-variant	RNF138	GRCh38.p7	18:32122262	GTGAACTGAGTGTCA[C/T]TGGAATGGTGCCTTT	51444
rs4799327	snp	A/G	0.287085	0.247234	intron-variant	RNF138	GRCh38.p7	18:32095029	ATCAACTTATTGTAC[A/G]TAGACAGTTCTGCCT	51444
rs4799328	snp	A/T	0.288906	0.246954	intron-variant	RNF138	GRCh38.p7	18:32122387	TTTTATAAAGGAAAA[A/T]TGAATAACCAGTTTA	51444
rs4799630	snp	A/G	0.287867	0.247116	intron-variant	RNF138	GRCh38.p7	18:32094606	CATTACCCATCTGAC[A/G]TGAAAAAAAAAACGT	51444
rs4799631	snp	A/G	0.441158	0.161117	intron-variant	RNF138	GRCh38.p7	18:32097902	tatgtatatgtgtat[A/G]tatgtgtatttgtgt	51444
rs4799632	snp	C/T	0.496714	0.0404017	intron-variant	RNF138	GRCh38.p7	18:32100930	TTAAATTAAAATAAA[C/T]GCTCAGAAAAATGGT	51444
rs5823831	snp	A/C	0.451483	0.148002	intron-variant	RNF138	GRCh38.p7	18:32121143	TGTCTCAAAAAAAAA[A/C]AAAACAAAAAAAAAG	51444
rs7228516	snp	C/T	0.0158469	0.0875917	intron-variant	RNF138	GRCh38.p7	18:32111069	acaggcgtgagccac[C/T]gtgcccggcAAAGCC	51444
rs7229437	snp	C/T	0.289165	0.246913	intron-variant	RNF138	GRCh38.p7	18:32118230	ggcattcttcatata[C/T]tctggatagtaatcc	51444
rs7229690	snp	A/G	0.00454277	0.047442	missense, intron-variant, nc-transcript-variant	RNF138	GRCh38.p7	18:32111885	AAAATATAATGAGGA[A/G]GTTTTCTGGTAGCTG	51444
rs7234604	snp	C/T	0.196771	0.244268	intron-variant	RNF138	GRCh38.p7	18:32110659	TCTAGATCCCAGATA[C/T]ATATGTCTGTAATTT	51444
rs7238559	snp	C/G	0.489837	0.0705577	intron-variant	RNF138	GRCh38.p7	18:32095830	TACTAAGTACTGTTT[C/G]TCTGGAGACTTAATA	51444
rs7243277	snp	C/T	0.0345262	0.126772	intron-variant	RNF138	GRCh38.p7	18:32126500	ATGTCTAAGATTTCT[C/T]ACTGTGTTAGATTAA	51444
rs7505481	snp	A/C	0.089084	0.191327	intron-variant	RNF138	GRCh38.p7	18:32121148	caaaaaaaaacaaaa[A/C]aaaaaaaaagcagat	51444
rs8085407	snp	C/T	0.44651	0.154543	intron-variant	RNF138	GRCh38.p7	18:32102490	acaggcgtgagccac[C/T]gtgcctggccCTTTT	51444
rs8095867	snp	A/G	0.44252	0.159487	upstream-variant-2KB, intron-variant	RNF138	GRCh38.p7	18:32092596	CCCGGCGCGTGCGGC[A/G]GTAGCGTCTCTGCGT	51444
rs8096674	snp	C/T	0.0158469	0.0875917	utr-variant-3-prime, nc-transcript-variant	RNF138	GRCh38.p7	18:32129712	ACTATAAGAAAATTG[C/T]ATTTATATAACATTT	51444
rs9953463	snp	C/T	0.447032	0.153878	intron-variant	RNF138	GRCh38.p7	18:32099096	TGGGAGAATGCGTAA[C/T]GGAAATTCGTCTAGC	51444
rs9954966	snp	A/C	0.0298908	0.118541	intron-variant	RNF138	GRCh38.p7	18:32096658	AAACTGAGGATTCAG[A/C]TCATCTGCAAATGAT	51444
rs9962021	snp	A/G	0.0260105	0.111035	intron-variant	RNF138	GRCh38.p7	18:32116071	gaggcgatgatgatg[A/G]taggtcctcattgag	51444
rs9963611	snp	C/T	0.0295035	0.117819	intron-variant	RNF138	GRCh38.p7	18:32095194	tttttttttgagaca[C/T]ggtcttattctgttg	51444
rs9964804	snp	C/T	0.185788	0.241613	intron-variant	RNF138	GRCh38.p7	18:32120587	GTAATTGATTTTCTA[C/T]TGTTGAACCTATTCT	51444
rs9967305	snp	A/C	0.0295035	0.117819	intron-variant	RNF138	GRCh38.p7	18:32105751	AAGTTAAAAAATTTC[A/C]ATATCGGAAGACCAC	51444
rs9967524	snp	A/T	0.497749	0.0334707	intron-variant	RNF138	GRCh38.p7	18:32096907	GGCTATTAAAAAAAA[A/T]TTTTTTGTAGAGATG	51444
rs10048285	snp	A/G	0.490063	0.0697833	intron-variant	RNF138	GRCh38.p7	18:32125746	AGACTAGCCTGGGCA[A/G]CATAGTGAGACCCTG	51444
rs10048287	snp	C/G	0.490007	0.0699769	intron-variant	RNF138	GRCh38.p7	18:32125761	ACATAGTGAGACCCT[C/G]TCTATTTAAAAATAA	51444
rs10647693	in-del	-/CTG	0.440746	0.161604	intron-variant	RNF138	GRCh38.p7	18:32107349	GCTGGTCTCGAACTC[-/CTG]AGCTCAGGCAGTCCG	51444
rs10663913	in-del	-/AAAAG	0.4444	0.15719	intron-variant	RNF138	GRCh38.p7	18:32128081	CTCAAAAAAGAAAAG[-/AAAAG]TAGGTGATCTAATTA	51444
rs10775450	snp	C/T	0.441568	0.160629	intron-variant	RNF138	GRCh38.p7	18:32105920	TGAAGCAAAGCACAT[C/T]AAAACATAGCTGAAT	51444
rs10853418	snp	C/T	0.489434	0.0719116	intron-variant	RNF138	GRCh38.p7	18:32118664	TGAAACCTTGTCTCT[C/T]CCAAAAATAGAAAAA	51444
rs10853419	snp	A/G	0.489259	0.0724914	intron-variant	RNF138	GRCh38.p7	18:32118702	GGCGTGGTGGTGCGC[A/G]CCTGTAATCCCAGCT	51444
rs11081743	snp	C/T	0.34989	0.229177	intron-variant	RNF138	GRCh38.p7	18:32101231	ttttttttttttttt[C/T]aaagacagagtctgg	51444
rs11081744	snp	C/T	0.000798403	0.0199641	intron-variant	RNF138	GRCh38.p7	18:32105804	TGATGGACTGAATGT[C/T]GTCTGTTCTACTTGC	51444
rs11081745	snp	A/C	0.133777	0.221342	intron-variant	RNF138	GRCh38.p7	18:32118753	AGAATTCCTTGAACC[A/C]GGGAGGCCAAGGTTG	51444
rs11081746	snp	C/G	0.490784	0.0672522	intron-variant	RNF138	GRCh38.p7	18:32124689	GAGAGCGTTATTTTT[C/G]TGTTATTCTGAATTA	51444
rs11307731	in-del	-/T	0.446771	0.154211	intron-variant	RNF138	GRCh38.p7	18:32113368	CAGCCAGGAACTTAA[-/T]TTTTTTTTAAGTGCT	51444
rs11375175	in-del	-/A	0	0	intron-variant	RNF138	GRCh38.p7	18:32103876	AGGCTGAGGCAGGAG[-/A]ATGGTGTGAACCCTG	51444
rs11441456	in-del	-/T	0.442249	0.159814	intron-variant	RNF138	GRCh38.p7	18:32094208	TTTTCTTTTTTTTTT[-/T]GAGGTGAGGTTCTAT	51444
rs11661197	snp	G/T	0.48955	0.071525	intron-variant	RNF138	GRCh38.p7	18:32116732	AATTTTTTGATTTTT[G/T]GGGGTGGGGGGGTGG	51444
rs11663518	snp	A/C	0	0	intron-variant	RNF138	GRCh38.p7	18:32110326	TGTTAATTGGTAATG[A/C]CTTCTAGTGCTGCTT	51444
rs11663563	snp	A/G	0.489608	0.0713316	intron-variant	RNF138	GRCh38.p7	18:32110463	GTTGTAGATACTTTT[A/G]TTATTTCGTGAGTGA	51444
rs12326277	snp	A/G	0	0	intron-variant	RNF138	GRCh38.p7	18:32124024	GAAGTTAGCAGTTTA[A/G]AAATAGAAAATGCAG	51444
rs12326287	snp	A/G			intron-variant	RNF138	GRCh38.p7	18:32124198	GATGCTTGATCCTCA[A/G]AATGTTTTCGAGTAT	51444
rs12326443	snp	C/T	0.127944	0.218179	upstream-variant-2KB	RNF138	GRCh38.p7	18:32091282	CTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTG	51444
rs12455044	snp	A/G	0.439406	0.163173	intron-variant	RNF138	GRCh38.p7	18:32112688	ACGCTGTCTAAAAAA[A/G]AAGAAGAAGAAAGAA	51444
rs12458837	snp	G/T	0.439502	0.163061	intron-variant	RNF138	GRCh38.p7	18:32105283	ttttagtagagacag[G/T]tttcaccatgttggc	51444
rs12458851	snp	C/G	0.439918	0.162576	intron-variant	RNF138	GRCh38.p7	18:32105480	TTTGGAACTTTTTAT[C/G]TTTGATAGACGTGAC	51444
rs12604223	snp	C/T	0.440195	0.162252	intron-variant	RNF138	GRCh38.p7	18:32123776	TCCTGCCTCAGCCTC[C/T]CAAGTATCTGGTATT	51444
rs12605137	snp	C/T	0.49681	0.0398085	intron-variant	RNF138	GRCh38.p7	18:32107051	TGTCTCCTATGGCTA[C/T]TGGGCCACTGGATTA	51444
rs12606789	snp	G/T	0.126564	0.217402	intron-variant	RNF138	GRCh38.p7	18:32114966	GTTCTCATTTTACTT[G/T]ACTTGTTAGTGTCAA	51444
rs12607933	snp	A/G	0.126909	0.217598	intron-variant	RNF138	GRCh38.p7	18:32099533	CCAATCTCCCGTGTA[A/G]CTGGAACTACAGGCA	51444
rs12608245	snp	G/T	0.126909	0.217598	intron-variant	RNF138	GRCh38.p7	18:32126028	AACTTTGGCTAGAGT[G/T]TAATTACTGAAGGTT	51444
rs12955597	snp	C/T			intron-variant	RNF138	GRCh38.p7	18:32102196	ccTTCTTTTAGtttc[C/T]ttttttttttttttt	51444
rs12961683	snp	G/T			intron-variant	RNF138	GRCh38.p7	18:32121220	ttcaatcctggccag[G/T]tgtggtggctcatgc	51444
rs12962037	snp	A/G			intron-variant	RNF138	GRCh38.p7	18:32098565	TAATTATATAATAAA[A/G]GTTGAggccgggcgc	51444
rs12962038	snp	G/T			intron-variant	RNF138	GRCh38.p7	18:32098569	TATATAATAAAGGTT[G/T]Aggccgggcgcagtg	51444
rs12962040	snp	C/G			intron-variant	RNF138	GRCh38.p7	18:32098579	AGGTTGAggccgggc[C/G]cagtggctcacgcct	51444
rs12962043	snp	A/G			intron-variant	RNF138	GRCh38.p7	18:32098582	TTGAggccgggcgca[A/G]tggctcacgcctgtc	51444
rs12962902	snp	G/T			intron-variant	RNF138	GRCh38.p7	18:32107112	AATTCACTTTCCttt[G/T]ttccttttttttttt	51444
rs12963443	snp	A/G	0.00676609	0.0577691	intron-variant	RNF138	GRCh38.p7	18:32125121	ATGAACCGGGAACTC[A/G]TTCCTGCGCAGTAGC	51444
rs12965634	snp	A/G	0.0410537	0.137264	intron-variant	RNF138	GRCh38.p7	18:32113267	tttgccatattgctc[A/G]ggctggtcttgaacc	51444
rs12966132	snp	G/T	0.375	0.216506	upstream-variant-2KB, utr-variant-3-prime	RNF138, RNF125	GRCh38.p7	18:32089992	ggctcaggcctgtaa[G/T]tccagcactttggga	51444
rs12967984	snp	A/G			intron-variant	RNF138	GRCh38.p7	18:32092897	CACGTGTGAGTAGAC[A/G]CCCCCTCCCCCTCGC	51444
rs12968984	snp	G/T			intron-variant	RNF138	GRCh38.p7	18:32108669	tatatgtaAtttttg[G/T]tttgtttggttttta	51444
rs12968986	snp	G/T	0	0	intron-variant	RNF138	GRCh38.p7	18:32108674	gtaAtttttgttttg[G/T]ttggtttttaaatag	51444
rs12969755	snp	A/G	0	0	intron-variant	RNF138	GRCh38.p7	18:32096497	AAGTGGTCACCGAGT[A/G]AGGTATATAAATGGA	51444
rs12969756	snp	G/T	0	0	intron-variant	RNF138	GRCh38.p7	18:32096500	TGGTCACCGAGTGAG[G/T]TATATAAATGGAAAG	51444
rs12970529	snp	G/T			intron-variant	RNF138	GRCh38.p7	18:32096473	ATGGAGCTAAAGCTG[G/T]GGGTGTCGAAGTGGT	51444
rs13381692	snp	G/T	0.0329836	0.124112	downstream-variant-500B	RNF138	GRCh38.p7	18:32131781	TTTTATGAAGTGTCT[G/T]CGGAGCAAGATTTTC	51444
rs16962689	snp	C/G	0.0158469	0.0875917	intron-variant	RNF138	GRCh38.p7	18:32110655	GTATTCTAGATCCCA[C/G]ATATATATGTCTGTA	51444
rs16962691	snp	C/T	0.0298908	0.118541	intron-variant	RNF138	GRCh38.p7	18:32111152	AAATTTCCCTACTTC[C/T]GGACCAAATAACCAA	51444
rs16962693	snp	A/C	0.0611083	0.163768	intron-variant	RNF138	GRCh38.p7	18:32111200	GATAACTTTGGGTAA[A/C]ACCTAACTTTGGGTA	51444
rs16962696	snp	A/C	0.00993419	0.0697739	intron-variant	RNF138	GRCh38.p7	18:32111578	TCTAGTCCAGTTATC[A/C]GTCTTACTCTCTGAT	51444
rs16962698	snp	C/G	0.00993419	0.0697739	intron-variant	RNF138	GRCh38.p7	18:32112358	GGAACTCTCTAGCTC[C/G]TCACTTTACTTATGT	51444
rs16962699	snp	A/G	0.192401	0.243274	intron-variant	RNF138	GRCh38.p7	18:32112911	AATTCAGTGAGCAAA[A/G]CTGGTTGCTATTTCA	51444
rs16962700	snp	A/C	0.123105	0.215401	intron-variant	RNF138	GRCh38.p7	18:32113559	CTTCTCCATCTCTAC[A/C]TTTAATGAACAGAAA	51444
rs16962701	snp	C/G	0.289424	0.246872	intron-variant	RNF138	GRCh38.p7	18:32115148	GGTGTTTGTCTTGTT[C/G]AGCATATCTCCAGCT	51444
rs16962717	snp	A/T	0.0596104	0.162024	intron-variant	RNF138	GRCh38.p7	18:32123139	TTGAAGTAAAAAAGT[A/T]CACAAATTCTTGAGT	51444
rs16962718	snp	A/G	0.0162398	0.0886349	intron-variant	RNF138	GRCh38.p7	18:32124170	CTGAAATTCAGAAGT[A/G]TTAAAACTCAGTGAT	51444
rs16962721	snp	C/T	0.00517822	0.0506191	intron-variant	RNF138	GRCh38.p7	18:32127690	ATTATTAAATTCTCA[C/T]TGTAAGAAAGATTGC	51444
rs17719020	snp	G/T	0.0429648	0.14013	intron-variant	RNF138	GRCh38.p7	18:32109023	ATTTATGCGCTCTAA[G/T]GGATATTGCCACCCA	51444

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