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
rs13151	snp	C/G	0.224738	0.24872	missense, nc-transcript-variant	RNF149	GRCh38.p7	2:101281950	TGATGGTGGACTGCT[C/G]TCATCACTTCCGTCA	284996
rs750783	snp	A/G	0.482459	0.0919928	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant, intron-variant	SNORD89, RNF149	GRCh38.p7	2:101272844	TGGGGACAATCACCT[A/G]TTCCTGAAGGTCTAT	284996
rs935065	snp	C/T	0.171057	0.237209	intron-variant	RNF149	GRCh38.p7	2:101282668	GGGACAGCTAGAAAC[C/T]TTATTTGATTAATAC	284996
rs1192792	snp	A/G	0.0923359	0.194016	intron-variant, utr-variant-3-prime	RNF149	GRCh38.p7	2:101280201	AATAATAATAATAAT[A/G]ATGATGATGATGATG	284996
rs1192793	snp	C/T	0.266	0.249487	intron-variant, utr-variant-3-prime	RNF149	GRCh38.p7	2:101281409	TCTCTACGTGGGGGA[C/T]GACTATTTTCATTTT	284996
rs1192794	snp	A/G	0.270892	0.249126	intron-variant, missense	RNF149	GRCh38.p7	2:101281760	ATAGCTCAAACTCGA[A/G]CAATCCTCCCACCTT	284996
rs1192795	snp	C/T	0.152001	0.229992	intron-variant	RNF149	GRCh38.p7	2:101284038	CCCACAAAGGCTCAT[C/T]CTCTCATCTAAGCTA	284996
rs1192796	snp	C/T	0.265727	0.249505	intron-variant	RNF149	GRCh38.p7	2:101285798	TACAAAACTAGCATA[C/T]ATACATTCTGTGGTG	284996
rs1192797	snp	C/T	0.268724	0.249298	intron-variant	RNF149	GRCh38.p7	2:101287074	CGCCTGTAATCCCAA[C/T]ATTTTGGGAGGCCGA	284996
rs1192808	snp	A/G	0.480853	0.0959518	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF149	GRCh38.p7	2:101275643	agacggggtttcacc[A/G]ttttagccgggatgg	284996
rs1192809	snp	A/G	0.264906	0.249555	intron-variant, utr-variant-3-prime	RNF149	GRCh38.p7	2:101278358	CTGCATGTTCCCCAG[A/G]CTGGCCTCATGCGAT	284996
rs1192828	snp	A/C	0.303438	0.244222	intron-variant	RNF149	GRCh38.p7	2:101295658	agtgcgagaccccat[A/C]tcaaaaaaaaaaaaa	284996
rs1660711	snp	A/G	0.47666	0.105476	downstream-variant-500B	RNF149	GRCh38.p7	2:101271029	cttgcttgtagtagg[A/G]gaggaaacggcaggg	284996
rs1660713	snp	A/G	0.266	0.249487	intron-variant	RNF149	GRCh38.p7	2:101289490	GGAGGGCGGATCATG[A/G]GGTCAGGAGATTGAG	284996
rs1726733	snp	A/T	0	0	intron-variant, utr-variant-3-prime	RNF149	GRCh38.p7	2:101281511	AAGACCCTGTCTCTT[A/T]AAAAAAAAAAAAAAA	284996
rs2056717	snp	A/G	0.473359	0.112298	intron-variant	RNF149	GRCh38.p7	2:101303817	GTTACAAAGAGGTAT[A/G]AGAAATCCCTCCTAT	284996
rs2177997	snp	C/T	0.476052	0.106772	intron-variant	RNF149	GRCh38.p7	2:101302340	ACCAAATTCACCTGC[C/T]AGGGAATCTCTTTAT	284996
rs3828194	snp	C/T	0.489186	0.0727321	intron-variant	RNF149	GRCh38.p7	2:101294923	GAAGTCAGGTAATGA[C/T]GGATAACTCTGAATT	284996
rs4851415	snp	C/T	0.250168	0.25	intron-variant	RNF149	GRCh38.p7	2:101287944	TACAATTTCTGTACA[C/T]AAAATGAACCCTTTT	284996
rs4851416	snp	A/G	0.499121	0.020948	intron-variant, upstream-variant-2KB	RNF149, MIR5696, LOC105373512	GRCh38.p7	2:101307542	AACTCAAGACTCAGG[A/G]AATCTGACTGGCAGT	284996
rs5832957	in-del	-/A/AA			downstream-variant-500B, nc-transcript-variant	RNF149	GRCh38.p7	2:101271617	GCACCACTGCACTCA[-/A/AA]AAAAAAAAAAAAAAA	284996
rs6543026	snp	C/T	0.231482	0.249313	upstream-variant-2KB, intron-variant	RNF149, LOC105373512	GRCh38.p7	2:101310495	TGCTTGTATGTATTA[C/T]GTTTGTACATTCATG	284996
rs6710491	snp	C/G	0.0130921	0.0798413	upstream-variant-2KB, intron-variant	SNORD89, RNF149	GRCh38.p7	2:101273500	ttttttttttgacag[C/G]gtctcactcttgccc	284996
rs6711606	snp	G/T	0.243633	0.249919	intron-variant	RNF149	GRCh38.p7	2:101305708	GGGGTGAGGGGGGTA[G/T]GAACAGGGAGGGAGA	284996
rs6713930	snp	A/G	0.354665	0.227036	upstream-variant-2KB, intron-variant	SNORD89, RNF149	GRCh38.p7	2:101273965	AAGCTTTTAAATTAA[A/G]GAACACTATGTTTGA	284996
rs6715956	snp	A/G	0.35574	0.226537	intron-variant	RNF149	GRCh38.p7	2:101282969	TGGCTGTGACATCAC[A/G]ATACCCAAACTCCTG	284996
rs6721662	snp	A/G	0.283158	0.247791	intron-variant	RNF149	GRCh38.p7	2:101305725	AACAGGGAGGGAGAG[A/G]GAGAGGAGGGGGAGA	284996
rs6737919	snp	C/T	0.354665	0.227036	intron-variant, downstream-variant-500B	RNF149	GRCh38.p7	2:101277760	GCCAACAAGAAAAAT[C/T]GGTAAACATCTTCAT	284996
rs6755716	snp	C/G	0.00557542	0.0525036	intron-variant	RNF149	GRCh38.p7	2:101294676	CACTCCTTTGGGTCT[C/G]GCAAGGGACTAAGAG	284996
rs7565185	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant, nc-transcript-variant	SNORD89, RNF149	GRCh38.p7	2:101274077	TTAAGAGAAACACCC[A/G]TCAAATTTATTGCAG	284996
rs7567834	snp	C/G	0.378372	0.214524	upstream-variant-2KB, intron-variant	RNF149, LOC105373512	GRCh38.p7	2:101310184	TAAAAGGCCCAAAGG[C/G]CCTCAGGCTTAAATT	284996
rs7568067	snp	A/G	0.378174	0.214642	upstream-variant-2KB, intron-variant	RNF149, LOC105373512	GRCh38.p7	2:101310349	ACTTCTTTCTCCCAT[A/G]ACCTGCTCCTGGCTC	284996
rs7587202	snp	C/T	0.0422008	0.138995	intron-variant, downstream-variant-500B	RNF149	GRCh38.p7	2:101277680	aggcatgagccaccg[C/T]gcccggctAACAGAA	284996
rs7598254	snp	A/G	0.0130921	0.0798413	downstream-variant-500B, intron-variant	RNF149	GRCh38.p7	2:101271765	AAAAAGAAGACAGCA[A/G]TGAGTAACATCTTAG	284996
rs8179876	snp	C/T	0.030665	0.119967	intron-variant	RNF149	GRCh38.p7	2:101289233	AGGATTATCTAAATA[C/T]GGTTGAAAAGGAAAA	284996
rs10186000	snp	C/T	0.473266	0.112482	intron-variant	RNF149	GRCh38.p7	2:101300620	GGAGTTTGACACCAG[C/T]CTGGGCAATATGGCA	284996
rs10496352	snp	A/G	0.0126979	0.078662	upstream-variant-2KB, intron-variant	SNORD89, RNF149	GRCh38.p7	2:101273911	TCTAGAGATATGACC[A/G]TAATTATTCCAACCT	284996
rs10496353	snp	C/T	0.47614	0.106587	intron-variant	RNF149	GRCh38.p7	2:101300997	CCACCCTTCCTTAAT[C/T]GGCACATGAGACCAA	284996
rs10706805	in-del	-/A	0.409212	0.192748	upstream-variant-2KB, intron-variant	RNF149, MIR5696, LOC105373512	GRCh38.p7	2:101309276	CAAATACATTTTGTG[-/A]AAAAAAAAAAAAAAA	284996
rs11123868	snp	A/G	0.491675	0.0639777	missense, upstream-variant-2KB, nc-transcript-variant	RNF149, MIR5696, LOC105373512	GRCh38.p7	2:101308564	CGGCGGCGCGAAGCC[A/G]GCGTCGGGGCTCGCG	284996
rs11340908	in-del	-/T	0.497855	0.0326773	intron-variant	RNF149	GRCh38.p7	2:101304858	TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCAC	284996
rs11422564	in-del	-/A	0.205417	0.245993	intron-variant, downstream-variant-500B	RNF149	GRCh38.p7	2:101278051	TATTATGAAGTATAC[-/A]AAAATCACTTCACAC	284996
rs11537547	snp	C/G	0.00092525	0.0214888	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF149, MIR5696, LOC105373512	GRCh38.p7	2:101308472	TCTCGAGTGGTTCTC[C/G]GCCGTGGTAAACATC	284996
rs11537548	snp	C/T	0	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF149	GRCh38.p7	2:101276921	AATTGGCTGCTATGG[C/T]TCTGTAAAAACCAGT	284996
rs11537549	snp	A/G			missense, upstream-variant-2KB, nc-transcript-variant	RNF149, MIR5696, LOC105373512	GRCh38.p7	2:101308366	AAGGAGGGCGCGCAT[A/G]GCCTGGTGGGCGTCC	284996
rs11692685	snp	A/C			intron-variant, utr-variant-3-prime	RNF149	GRCh38.p7	2:101278430	ttacaagtgtgagcc[A/C]ccatgtccagccTGA	284996
rs11903744	snp	A/G	0.330714	0.236612	downstream-variant-500B	RNF149	GRCh38.p7	2:101271071	GCCTCCGTCAGGAAC[A/G]TGCGGGTCAGGCAGC	284996
rs12327984	snp	A/G	0.039522	0.134904	intron-variant, utr-variant-3-prime	RNF149	GRCh38.p7	2:101280881	ttcaaaaaaatttaa[A/G]aagttagctagatgt	284996
rs12611674	snp	C/G	0.030665	0.119967	utr-variant-3-prime, intron-variant	RNF149	GRCh38.p7	2:101271927	TTTACACCTAATTTT[C/G]AGTAGCACACTAAAT	284996
rs12612035	snp	A/G	0.470132	0.118498	intron-variant, utr-variant-3-prime	RNF149	GRCh38.p7	2:101280833	AATTTAAAAAATGCA[A/G]TGAGTCTAGACAACA	284996
rs12616551	snp	C/T	0.030665	0.119967	intron-variant	RNF149	GRCh38.p7	2:101285411	CTGCATGACCTCAGG[C/T]GAGTTATTTAGCTTC	284996
rs12617343	snp	C/T	0.478104	0.102316	intron-variant	RNF149	GRCh38.p7	2:101300903	GGCACGGGCACCTTG[C/T]GGGCCCTACTCTTGC	284996
rs12620272	snp	A/G	0.0310518	0.120672	intron-variant	RNF149	GRCh38.p7	2:101292489	CTGCAATTTCCggcc[A/G]ggcgtggtggctcac	284996
rs12621632	snp	C/T	0.472989	0.113031	intron-variant, utr-variant-3-prime	RNF149	GRCh38.p7	2:101280863	ATGGTGAGACTTCAT[C/T]ACTTCAAAAAAATTT	284996
rs12621727	snp	A/G	0.00938946	0.0678717	utr-variant-3-prime, intron-variant	RNF149	GRCh38.p7	2:101272390	CAAGTCTCCAGCTGC[A/G]TGGCTGATTATGACA	284996
rs12622282	snp	C/T	0.030665	0.119967	utr-variant-3-prime, intron-variant	RNF149	GRCh38.p7	2:101271897	CGATTTTTATTCTTA[C/T]AGTGTACATATACAT	284996
rs12712092	snp	C/G	0.482609	0.0916147	downstream-variant-500B	RNF149	GRCh38.p7	2:101270819	AAAACACTGAACTCA[C/G]AGCCAACACCATCAC	284996
rs12712093	snp	C/T	0.481627	0.0940692	intron-variant	RNF149	GRCh38.p7	2:101284542	GCCAAGATCACGCCA[C/T]TGAACTCCAGCCTCG	284996
rs12712094	snp	A/C	0.481627	0.0940692	intron-variant	RNF149	GRCh38.p7	2:101284587	CTGTCTCAAAAAAAA[A/C]CAAACAAATCATAAT	284996
rs12993198	snp	A/T			downstream-variant-500B, intron-variant	RNF149	GRCh38.p7	2:101275426	ccggccCTCCCCTAG[A/T]ATTTCtttttttttt	284996
rs12993457	snp	A/G	0.474272	0.110462	intron-variant	RNF149	GRCh38.p7	2:101305898	AGAGTGAGTCACTCT[A/G]TGCAGAACACTGAGC	284996
rs13017536	snp	C/T	0.474903	0.109173	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF149	GRCh38.p7	2:101275676	TCGATCTCCTGACCT[C/T]GTGATCCGCCCGCCT	284996
rs13031025	snp	A/G	0.476052	0.106772	intron-variant	RNF149	GRCh38.p7	2:101301049	AAATGACTGGATTTC[A/G]TCACAGAAACTCAAA	284996
rs13389242	snp	C/T	0.000399281	0.0141238	intron-variant	RNF149	GRCh38.p7	2:101291370	tggccaagctggtct[C/T]gaactcctgacctcg	284996
rs13395927	snp	C/T			intron-variant	RNF149	GRCh38.p7	2:101292972	GCCATGAGATGTGAt[C/T]ttttttttttttttt	284996
rs13400007	snp	C/T	0	0	intron-variant	RNF149	GRCh38.p7	2:101294370	CTGATTTTAATTTGT[C/T]TGAAGAAGCAACCAC	284996
rs13410929	snp	C/T	0.0364509	0.129988	intron-variant	RNF149	GRCh38.p7	2:101297488	cagcttcctgagcag[C/T]tgggaccacaggcac	284996
rs17020684	snp	C/T	0.268724	0.249298	intron-variant	RNF149	GRCh38.p7	2:101287645	TAACTTTCTACATGA[C/T]ATGATCAACTTATAC	284996
rs17025374	snp	C/T	0.189576	0.242588	intron-variant	RNF149	GRCh38.p7	2:101299765	ACACGTTCACATTTA[C/T]GTCTCACTTGAAGCA	284996
rs17025378	snp	C/G	0.253544	0.249975	intron-variant	RNF149	GRCh38.p7	2:101303077	CCCACCCTCTGTGAG[C/G]CTATGAGGTGCCATT	284996
rs17190139	snp	A/G	0.0524604	0.153226	intron-variant	RNF149	GRCh38.p7	2:101294830	TTAAATAATATAAGC[A/G]AAAATCAAGATTATG	284996
rs17190412	snp	C/T	0.498908	0.0233371	intron-variant	RNF149	GRCh38.p7	2:101306311	ATGGCACACTAACCT[C/T]TTTTCTTTGACAGAA	284996
rs17190440	snp	A/G	0.0260105	0.111035	intron-variant	RNF149	GRCh38.p7	2:101306418	TCTTGTGCAAACGCA[A/G]CCTGGGTACCGTGAC	284996
rs17856945	snp	A/C	0	0	missense, nc-transcript-variant	RNF149	GRCh38.p7	2:101281986	TGGTAAAGCTAGACT[A/C]AAATTTGCAGCTGGA	284996
rs28626790	snp	C/T	0.000623268	0.0176422	intron-variant	RNF149	GRCh38.p7	2:101289084	AGGAAAGTGTTACTA[C/T]ATTCTTGGTACACAG	284996
rs34103366	in-del	-/T	0.49703	0.0384237	intron-variant	RNF149	GRCh38.p7	2:101292973	CCATGAGATGTGATC[-/T]TTTTTTTTTTTTTTT	284996
rs34268551	in-del	-/G			intron-variant, upstream-variant-2KB	RNF149, MIR5696, LOC105373512	GRCh38.p7	2:101307520	TAATTTTAAAATTTT[-/G]GATCGTAACTCAAGA	284996
rs34632783	in-del	-/C	0.226484	0.248892	intron-variant	RNF149	GRCh38.p7	2:101277505	GCGATTCTCCTGCCT[-/C]AGCCTCCTGGGTAGC	284996
rs34671786	snp	A/T	0.00398564	0.0444627	intron-variant	RNF149	GRCh38.p7	2:101287904	TAGGTGTGAAGTATA[A/T]TTAAAATTCATCAGA	284996
rs34737780	in-del	-/G	0.481703	0.0938806	intron-variant	RNF149	GRCh38.p7	2:101297547	TTTTTTTTTAGAGAT[-/G]GGGGTCTCACTATGT	284996
rs34738132	in-del	-/T			intron-variant, utr-variant-3-prime	RNF149	GRCh38.p7	2:101279500	AGAAGGCAAAGTTAG[-/T]TTTTCTTTCTGGAGT	284996
rs35054162	in-del	-/G			intron-variant	RNF149	GRCh38.p7	2:101285586	GTGTCTTCTGTGTAA[-/G]GGCCCTGTGACCATC	284996
rs35208977	in-del	-/G			intron-variant	RNF149	GRCh38.p7	2:101296524	AGACACCCACAGAAT[-/G]GAGACAGAATAAAAG	284996
rs35341790	in-del	-/G			intron-variant	RNF149	GRCh38.p7	2:101302475	GCAATATTATGTTTT[-/G]GGACAATTTGTCTTG	284996
rs35379583	in-del	-/C	0.481473	0.0944461	intron-variant	RNF149	GRCh38.p7	2:101282985	ATACCCAAACTCCTG[-/C]CCAGCCTAGCTCCAA	284996
rs35448871	in-del	-/A			intron-variant	RNF149	GRCh38.p7	2:101294899	TATGAATTATCTTTT[-/A]AAAAGCAAAATTCAG	284996
rs35758721	snp	A/G			intron-variant, utr-variant-3-prime	RNF149	GRCh38.p7	2:101280935	GCTACTTGGGAGGCA[A/G]AGGTGGCAGGATTGG	284996
rs35779324	in-del	-/G			intron-variant	RNF149	GRCh38.p7	2:101300241	CAACAAAATATATTT[-/G]GGGATGGTGACCAGC	284996
rs35820810	snp	C/T			upstream-variant-2KB, intron-variant	RNF149, MIR5696, LOC105373512	GRCh38.p7	2:101309078	TGGCAGAGGCCTTGT[C/T]TAAGTCGTTTCAAAG	284996
rs35878898	in-del	-/G			nc-transcript-variant, downstream-variant-500B	RNF149	GRCh38.p7	2:101271214	CAAAATCACAATATT[-/G]GGTGTTTACTTGAAA	284996
rs35994862	in-del	-/A			intron-variant	RNF149	GRCh38.p7	2:101296621	CAAAATGAATTATTT[-/A]AAAAATCACGTGGGG	284996
rs56156633	snp	A/G			intron-variant, utr-variant-3-prime	RNF149	GRCh38.p7	2:101281646	GCTGGGACTACAGGA[A/G]AATGCCACCATACCT	284996
rs56199522	snp	C/T			intron-variant	RNF149	GRCh38.p7	2:101295369	TAATAGAATAAATCA[C/T]TAAGAACTATTCCCC	284996
rs56736067	snp	C/T	0.222333	0.248464	intron-variant	RNF149	GRCh38.p7	2:101303829	TCTTATACCTCTTTG[C/T]AACCTCCCCTGCCAC	284996
rs57202124	snp	A/G	0.0130921	0.0798413	downstream-variant-500B, intron-variant	RNF149	GRCh38.p7	2:101275413	TGAGCCACCGCGCCC[A/G]GCCCTCCCCTAGTAT	284996
rs57224969	in-del	-/T			intron-variant	RNF149	GRCh38.p7	2:101303297	TTTTTTTTTTTTTTT[-/T]GTATTTTTAGTAGAG	284996
rs58511902	in-del	-/AA	0.332568	0.235971	intron-variant	RNF149	GRCh38.p7	2:101302982	GAGACACTTGTCTCT[-/AA]AAAAAAAAAAAAAAC	284996
rs59154104	in-del	-/TT			downstream-variant-500B, intron-variant	RNF149	GRCh38.p7	2:101275458	TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTCGC	284996
rs59164698	in-del	-/TT			intron-variant	RNF149	GRCh38.p7	2:101303282	CTCAACGTTGGCTCA[-/TT]TTTTTTTTTTTTTTG	284996
rs59230666	snp	A/G	0.000399281	0.0141238	intron-variant	RNF149	GRCh38.p7	2:101305966	TCTTTAAATTGTTTC[A/G]TTGGTCTTTTCTCTC	284996

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