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
rs1317843	snp	C/T	0.341235	0.232758	intron-variant	LRSAM1	GRCh38.p7	9:127490007	AAAGTGACCTCGGCC[C/T]AGGAGGAGGCGGTCC	90678
rs1317844	snp	C/T	0.183886	0.241099	intron-variant	LRSAM1	GRCh38.p7	9:127490033	GGTCCTCCTCTTAGA[C/T]CCTCCCTCATGTGAC	90678
rs1539564	snp	C/T	0.45866	0.137698	intron-variant	LRSAM1	GRCh38.p7	9:127491652	GCCCTGGAGGATGTG[C/T]GCCTGGGGGCCTAAA	90678
rs1539567	snp	C/T	0.345853	0.230894	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479887	GCTGCCGCTCTGCGT[C/T]GAGGTGGCGCTGGTG	90678
rs1539568	snp	A/G	0.488218	0.0758443	intron-variant	LRSAM1	GRCh38.p7	9:127479830	ACTGCTCCTGCAGCC[A/G]GAGGTAGGGGTCCTG	90678
rs1539569	snp	A/G	0.345065	0.23122	intron-variant	LRSAM1	GRCh38.p7	9:127479543	GCCACTGGCTGGGGG[A/G]TGCAGCCAGGCTGGA	90678
rs1547840	snp	A/T	0.471673	0.115589	intron-variant	LRSAM1	GRCh38.p7	9:127490028	ATGAGGGAGGGTCTA[A/T]GAGGAGGACCGCCTC	90678
rs1547841	snp	C/G	0.394538	0.203982	intron-variant	LRSAM1	GRCh38.p7	9:127489971	AGGCGTCAGGACCAC[C/G]GTGGCTCACAGCTCC	90678
rs2243464	snp	A/T	0.458545	0.137872	intron-variant	LRSAM1	GRCh38.p7	9:127486087	TGTGGTTCATCGCTT[A/T]GCCGAGTGCCTGCCA	90678
rs2243509	snp	C/G	0.432944	0.170387	intron-variant	LRSAM1	GRCh38.p7	9:127454771	CTGCCAAGGGTGCTT[C/G]TCCCCTGTAGACTGA	90678
rs2243608	snp	C/T	0.493013	0.058691	intron-variant	LRSAM1	GRCh38.p7	9:127464630	TCTCGACATCTAGTA[C/T]GAGTTCTGGACACTT	90678
rs2243663	snp	A/G	0.493837	0.055168	intron-variant	LRSAM1	GRCh38.p7	9:127460173	cctggctaatttttt[A/G]tattttagtagagac	90678
rs2243767	snp	C/T	0.484801	0.0858387	intron-variant	LRSAM1	GRCh38.p7	9:127459109	CCACCTCGGATGGCC[C/T]TAGTGAGACCAGGCA	90678
rs2243784	snp	A/G	0.49306	0.0584955	intron-variant	LRSAM1	GRCh38.p7	9:127458677	CTGTGGAGTACCACT[A/G]TCAATATTTTATCGC	90678
rs2243898	snp	C/G	0.492188	0.0620098	intron-variant	LRSAM1	GRCh38.p7	9:127457711	GAAGAGGAGGGACGC[C/G]CAGGTGATCTGGAAG	90678
rs2243903	snp	C/T	0.49263	0.0602539	intron-variant	LRSAM1	GRCh38.p7	9:127457464	CTGAGCGCCTGCTCC[C/T]TTTGGGCTGCCTCTT	90678
rs2243906	snp	C/T	0.484948	0.0854709	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127457390	GAGTCTGGCAACCAT[C/T]AAGGTACTGGGCCCT	90678
rs2244218	snp	G/T	0.449345	0.150869	intron-variant	LRSAM1	GRCh38.p7	9:127454672	GTAGGCCTCCGCACT[G/T]CCCCCAACAAGCCGT	90678
rs2244331	snp	G/T	0.455621	0.142197	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453841	AAGAACTAGAAAGAC[G/T]CAGCCCCTCACCTCA	90678
rs2244468	snp	A/G	0.493703	0.0557558	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453000	GGTCAGGACTTGAGA[A/G]ACCACGGTTCCAGGC	90678
rs2244624	snp	A/G	0.492533	0.0606443	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451229	CTTTGCACGCGCGGC[A/G]GGGCCGAGGGATGCT	90678
rs2245461	snp	A/G	0.44858	0.151875	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503809	GCAGCTGAGGCTGAT[A/G]GGGGTAAATGCTCAG	90678
rs2245645	snp	A/G	0.00597247	0.0543191	intron-variant	LRSAM1	GRCh38.p7	9:127502151	CCTCCGGCAGGGGCC[A/G]GCGGAATAGGCCTCC	90678
rs2245677	snp	A/G	0.455024	0.143057	intron-variant	LRSAM1	GRCh38.p7	9:127489233	GGAAACTCAGGGTGC[A/G]ATGCCGGAAGTGCAT	90678
rs2246000	snp	A/G	0.487432	0.0782705	intron-variant	LRSAM1	GRCh38.p7	9:127486865	TTCATAATAGCAACT[A/G]TTTTTTCCCAGTGAG	90678
rs2246011	snp	C/T	0.499902	0.00698814	intron-variant	LRSAM1	GRCh38.p7	9:127486606	CCCCCTTTCCTGATA[C/T]GTGACACTGTGCTTA	90678
rs2246267	snp	C/T	0.395087	0.203592	intron-variant	LRSAM1	GRCh38.p7	9:127484381	TGCCACATTTTCTTT[C/T]TTTCTTTTTTCCTTG	90678
rs2246270	snp	C/T	0.394904	0.203722	intron-variant	LRSAM1	GRCh38.p7	9:127484285	TTTTTTTTTTTCCTG[C/T]TTCTTTATTTCTAAA	90678
rs2246375	snp	G/T	0.456095	0.141508	intron-variant	LRSAM1	GRCh38.p7	9:127483508	TTTAAATAAATGTTG[G/T]TGATCCATATGCTGT	90678
rs2246579	snp	A/T	0.486725	0.0803809	intron-variant	LRSAM1	GRCh38.p7	9:127481976	CAGAAAAAAAATCTA[A/T]ATTTCTGGAAAGAAA	90678
rs2246600	snp	A/G	0.458084	0.138567	intron-variant	LRSAM1	GRCh38.p7	9:127481567	AGAGCAGCTTTGAGG[A/G]GAGAATGTCTTGTGA	90678
rs2247303	snp	A/G	0.492679	0.0600586	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451019	CGCTAACCCAGGCCA[A/G]TGGGGCGAAACGCCC	90678
rs2247310	snp	C/G	0.493599	0.0562105	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450831	GAAGAGTTAGTGTCT[C/G]TGCAGAGGGAGCCCC	90678
rs2247322	snp	A/T	0.493523	0.0565391	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450597	AAGGTACCTAGTACT[A/T]GTTCAGTGGCTCAGG	90678
rs2248725	snp	C/T	0.454904	0.143228	intron-variant	LRSAM1	GRCh38.p7	9:127498509	CAGCAGTCCTCAGGA[C/T]CGGCTGCTTCTCACT	90678
rs2248822	snp	A/C	0.349407	0.229396	intron-variant	LRSAM1	GRCh38.p7	9:127497339	GATCCAGCCAGGTAC[A/C]AGCACAGCTCCAGCC	90678
rs2249052	snp	A/T	0.458084	0.138567	intron-variant	LRSAM1	GRCh38.p7	9:127495881	ATGTATTATGTTATA[A/T]ATATTCAAACCCTTC	90678
rs2249282	snp	C/G	0.394904	0.203722	intron-variant	LRSAM1	GRCh38.p7	9:127493531	CTTTCTCAAGGCTGT[C/G]CGTGGCCCCTATTGT	90678
rs2249290	snp	C/T	0.451109	0.148509	intron-variant	LRSAM1	GRCh38.p7	9:127493289	CTGGTCTCCAACTCC[C/T]GGGCTCAAACGATCT	90678
rs2249649	snp	A/G	0.396364	0.202676	intron-variant	LRSAM1	GRCh38.p7	9:127478701	AAGAGCCCCTCCTAC[A/G]GTGCCATGCACACAG	90678
rs2249791	snp	A/G	0.398174	0.201356	intron-variant	LRSAM1	GRCh38.p7	9:127478040	ctgggcaacaagagc[A/G]aaactccgtctcaaa	90678
rs2249803	snp	A/G	0.456095	0.141508	intron-variant	LRSAM1	GRCh38.p7	9:127477621	caggcatggtggtgc[A/G]tgcctgcagtctcag	90678
rs2249936	snp	C/G	0.449853	0.150196	intron-variant	LRSAM1	GRCh38.p7	9:127476366	GCCTGGGCAATGTGG[C/G]GAGACCCTGTCTCTA	90678
rs2249940	snp	A/G	0.487241	0.0788465	intron-variant	LRSAM1	GRCh38.p7	9:127476261	TCGGCTCGCTGGGAC[A/G]CATGGATTAGTGAAA	90678
rs2250020	snp	C/T	0.457853	0.138915	intron-variant	LRSAM1	GRCh38.p7	9:127475881	gagtagctgggatta[C/T]agggatgcgccacca	90678
rs2250021	snp	C/T	0.457853	0.138915	intron-variant	LRSAM1	GRCh38.p7	9:127475843	tctcccgggttcaag[C/T]gattctcctgcctca	90678
rs2250024	snp	A/T	0.487177	0.0790385	intron-variant	LRSAM1	GRCh38.p7	9:127475745	aagattttattattt[A/T]tttatttttttttga	90678
rs2250161	snp	C/T	0.456622	0.140738	intron-variant	LRSAM1	GRCh38.p7	9:127475077	ATTATTATTATTTTA[C/T]AGTTCAGCAAGAATT	90678
rs2250184	snp	C/G	0.4582	0.138394	intron-variant	LRSAM1	GRCh38.p7	9:127474310	TCTTGCTCCATCACC[C/G]AGGCTGGAGTGCAGT	90678
rs2250267	snp	A/G	0.487889	0.0768691	intron-variant	LRSAM1	GRCh38.p7	9:127473964	GCTGCACGCATACAT[A/G]TGTGTGTGTGCGTGT	90678
rs2250271	snp	A/G	0.00475057	0.0485048	intron-variant	LRSAM1	GRCh38.p7	9:127473739	TGGCAGTGGGAGCGG[A/G]TGTCTCTGGGTACCT	90678
rs2253411	snp	C/G	0.431621	0.171796	intron-variant	LRSAM1	GRCh38.p7	9:127470630	TGTCCATTAGGAGTA[C/G]AATGGATAACTAAAC	90678
rs2253414	snp	A/T	0.431473	0.171952	intron-variant	LRSAM1	GRCh38.p7	9:127470611	aacctggaaacagct[A/T]taatgtccattagga	90678
rs2253639	snp	A/G	0.492484	0.0608394	intron-variant	LRSAM1	GRCh38.p7	9:127469138	ATCCTACAGATCCAC[A/G]AGGAAAAGACATTAG	90678
rs2253669	snp	A/G	0.490398	0.0686206	intron-variant	LRSAM1	GRCh38.p7	9:127468235	GAGAAGAGAGATGGG[A/G]GAAGCCAAAGACAGT	90678
rs2253806	snp	A/G	0.491834	0.0633738	intron-variant	LRSAM1	GRCh38.p7	9:127467373	ctgctggtgcagctc[A/G]cctcaatatcttatc	90678
rs2253811	snp	A/C	0.456685	0.140646	intron-variant	LRSAM1	GRCh38.p7	9:127467285	aaacagttccaggtg[A/C]aggggcttaaactat	90678
rs2253898	snp	A/G	0.465788	0.126237	intron-variant	LRSAM1	GRCh38.p7	9:127466983	GTCTGGGCAATGGGA[A/G]TGAGACCCTGTCTCA	90678
rs2253928	snp	C/G	0.493013	0.058691	intron-variant	LRSAM1	GRCh38.p7	9:127466290	CTCCAGCCTGCCACA[C/G]AGCAAGACTCTGTCT	90678
rs2253929	snp	C/T	0.492918	0.0590819	intron-variant	LRSAM1	GRCh38.p7	9:127466232	GAGAATTGCTTGAAC[C/T]GGGGAGGCAAAGGTT	90678
rs2253930	snp	A/G	0.4661	0.125701	intron-variant	LRSAM1	GRCh38.p7	9:127466216	CGGGAGGCTGAGGCA[A/G]GAGAATTGCTTGAAC	90678
rs2254041	snp	C/T	0.492966	0.0588865	intron-variant	LRSAM1	GRCh38.p7	9:127466165	AATACAAAAATTAGC[C/T]GGGTGTGGTGGCGCA	90678
rs2254164	snp	A/T	0.465892	0.126058	intron-variant	LRSAM1	GRCh38.p7	9:127464800	GGTGTACCCCATCAC[A/T]CTTGGCTAATTTTTT	90678
rs2254437	snp	A/G	0.49306	0.0584955	intron-variant	LRSAM1	GRCh38.p7	9:127462648	AAGAAAGTTGTCGGT[A/G]GGGGAACAACACAGT	90678
rs2254541	snp	A/G	0.332106	0.236133	intron-variant	LRSAM1	GRCh38.p7	9:127461475	CTGAGAGCCAGGGCC[A/G]TATGGCCGTATGGGG	90678
rs2255483	snp	A/G	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127460339	GTGTGTCATCCTGCT[A/G]GCCTTGCTCACCTCG	90678
rs2265685	snp	C/T	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127458382	cgacagagcgagact[C/T]cgtctcaaaaacaaa	90678
rs2265687	snp	A/G	0.030665	0.119967	intron-variant	LRSAM1	GRCh38.p7	9:127469435	agattgtgccactgc[A/G]ctccagtctggatga	90678
rs2265688	snp	A/G	0.488241	0.0757703	intron-variant	LRSAM1	GRCh38.p7	9:127500318	GTGAGCCGAGATCGC[A/G]CCACTGAACTCCAGC	90678
rs2488899	snp	A/T	0.493837	0.055168	intron-variant	LRSAM1	GRCh38.p7	9:127459419	agatggtgtttcgcc[A/T]tgttggcctgactgg	90678
rs2488900	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127466494	tatatatatatatat[A/T]ttttttttttttttt	90678
rs2488901	snp	C/T	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127466531	TTTTTTTTTTTTTTT[C/T]CACTAGAGATGGGGT	90678
rs2488902	snp	C/T	0.432357	0.171014	intron-variant	LRSAM1	GRCh38.p7	9:127498806	gctcacacctgtaat[C/T]ccagcactttgggag	90678
rs2488903	snp	A/G	0.489665	0.0711382	intron-variant	LRSAM1	GRCh38.p7	9:127499797	cagtggcgtgtgcct[A/G]tagtcccagatacgc	90678
rs2491101	snp	C/T	0.455502	0.142369	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452970	TGAGCACCAAGCAGT[C/T]GGGCAAATCCCATAG	90678
rs2798428	snp	C/T	0.487305	0.0786545	intron-variant	LRSAM1	GRCh38.p7	9:127494926	ATGATGGTTATGAAC[C/T]ATGCTCCTCTGAGCG	90678
rs2798429	snp	C/T	0.455144	0.142885	intron-variant	LRSAM1	GRCh38.p7	9:127494912	CCATGCTCCTCTGAG[C/T]GGGTGGACAGCACTT	90678
rs2798430	snp	A/T	0.449091	0.151204	intron-variant	LRSAM1	GRCh38.p7	9:127458600	TTTTTAATTTAATTT[A/T]ATTTTATTTTGTTTT	90678
rs2806714	snp	A/C	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127468834	aaaaaaaaaaaaaaa[A/C]aaaaatcagccaggc	90678
rs2995822	snp	A/G	0.455858	0.141853	intron-variant	LRSAM1	GRCh38.p7	9:127472355	CTTTTAAAAAACATT[A/G]AAGAGGCTGGGCATG	90678
rs2995823	snp	A/G	0.486984	0.079614	intron-variant	LRSAM1	GRCh38.p7	9:127472368	TTAAAGAGGCTGGGC[A/G]TGGTGACTCACACCT	90678
rs3053015	in-del	-/TC	0.375	0.216506	intron-variant	LRSAM1	GRCh38.p7	9:127489560	GCCACTCTGCAAGTC[-/TC]TGAGAGAGCAGGTCC	90678
rs3053020	in-del	-/GT/TG			intron-variant	LRSAM1	GRCh38.p7	9:127479096	AGGATGCAGCAGACT[-/GT/TG]GCGTGTAAGAGGAAG	90678
rs3802358	snp	C/T	0.248416	0.249995	intron-variant	LRSAM1	GRCh38.p7	9:127497377	CAGAGCCCACACATA[C/T]GGCTGGAGCCCTGCC	90678
rs3802360	snp	C/T	0.00163535	0.0285482	intron-variant	LRSAM1	GRCh38.p7	9:127497215	AGACTGTGGCCTGGG[C/T]GGGAGCCCGCTAAAT	90678
rs3802361	snp	A/G	0.00954246	0.0684118	intron-variant	LRSAM1	GRCh38.p7	9:127496131	GGACAGCGGCCTTGC[A/G]TGCCCCTCCCCTCCA	90678
rs3808831	snp	A/G	0.242488	0.249887	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452135	GTCCAGCCTAGATGC[A/G]GGGGGAGGGCCACAC	90678
rs3808832	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	RPL12, LRSAM1	GRCh38.p7	9:127451550	CAGCGCACCGCGGTG[C/T]CCTGCTTGCCAGCCG	90678
rs3808833	snp	A/C/T	0.0205649	0.0992992	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451369	GAGGCCAAGGTGCAA[A/C/T]TTCCTTCGGTCGTCC	90678
rs3808834	snp	C/T	0.000308732	0.0124206	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451322	CGACACCAGCCGCCT[C/T]CACCATGCCGCCGAA	90678
rs3840733	in-del	-/C	0.247265	0.249985	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452325	AAACAGCCCTCCCCC[-/C]ATCCGTCCCTGATGA	90678
rs3935304	snp	A/G	0.318174	0.240525	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503966	CAGAGGTGCACGTTG[A/G]TTATGCATTTTCCGG	90678
rs4836563	snp	A/G	0.257176	0.249897	intron-variant	LRSAM1	GRCh38.p7	9:127492401	TTTCCAAGAGCAGGC[A/G]CAGGAGTGAAGCAGG	90678
rs4836564	snp	A/G	0.284471	0.247612	intron-variant	LRSAM1	GRCh38.p7	9:127493227	CCACCATGCCTGGCA[A/G]ATTTTTTTATTTTTT	90678
rs4837153	snp	C/T	0.316	0.241131	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451143	CAGAAAGGCTGAGGC[C/T]TGGCCGGGGCGGCGC	90678
rs4837154	snp	G/T	0.245346	0.249957	intron-variant	LRSAM1	GRCh38.p7	9:127457130	CCCTTGAAGATCCAG[G/T]TTTTAAGGAAGGGCA	90678
rs4837155	snp	C/T	0.0433465	0.140692	intron-variant	LRSAM1	GRCh38.p7	9:127469593	ATACTTTGACAAACC[C/T]ACTAAAATGGCCAGA	90678
rs5900748	in-del	-/A	0.394538	0.203982	intron-variant	LRSAM1	GRCh38.p7	9:127491007	ACAAGCACGTCCATG[-/A]CCCCAGGAACGCGAG	90678
rs7019372	snp	C/T	0.0128825	0.0792169	intron-variant	LRSAM1	GRCh38.p7	9:127501175	CCCCACCCGCCTGCC[C/T]TGCCTGTGGCCACCC	90678
rs7023786	snp	A/G	0.0501905	0.150254	intron-variant	LRSAM1	GRCh38.p7	9:127477906	tacagaaaatcagcc[A/G]ggtgtggtggtgggt	90678

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