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
rs15834	snp	G/T	0.282632	0.247861	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462504	TATATAAACAAAATA[G/T]CCATATCTGATTTTT	84708
rs366074	snp	C/G	0.305685	0.24372	intron-variant	LNX1	GRCh38.p7	4:53565967	AGAATAAAAAGAAAC[C/G]AGCAAAGCCTCCAAG	84708
rs716251	snp	A/T	0.265727	0.249505	intron-variant	LNX1	GRCh38.p7	4:53555893	GTAGAAGAGAAAATT[A/T]TTAAGTGGTATAAGG	84708
rs727943	snp	A/C	0.248784	0.253684	intron-variant	LNX1	GRCh38.p7	4:53556272	AGGAACACCTGCAGC[A/C]CCCCCCTCCACAAAA	84708
rs750695	snp	A/G	0.499631	0.0135733	intron-variant	LNX1	GRCh38.p7	4:53637601	TTGTTTCATTACTAC[A/G]GAATTTCATCACTTC	84708
rs769072	snp	A/C	0	0	intron-variant	LNX1	GRCh38.p7	4:53530816	CAAATTACATAGTGT[A/C]TAGAATTTGCTTTAA	84708
rs907505	snp	A/G	0	0	intron-variant	LNX1	GRCh38.p7	4:53637616	ccctttggcatctta[A/G]aagtgatgaaatTCT	84708
rs907506	snp	G/T	0.0825414	0.185628	intron-variant	LNX1	GRCh38.p7	4:53531376	TTTTCCAGAGCCACA[G/T]TCCTCTCATCTATAA	84708
rs907509	snp	A/C	0.418007	0.185132	intron-variant	LNX1	GRCh38.p7	4:53587231	CTTTCTGTGTTTACC[A/C]TTTCCTCCATTTTGT	84708
rs907510	snp	G/T	0.28052	0.24813	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603251	GACTCCTCACTGCAT[G/T]TGAGGACCTACTCAT	84708
rs907511	snp	G/T	0.38286	0.211774	intron-variant	LNX1	GRCh38.p7	4:53572599	GAAATTTGGAAGATG[G/T]TGTTTATCCTGGTTC	84708
rs925477	snp	C/T	0.38286	0.211774	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596501	TGTTTATAATGGTCA[C/T]GAGACCTATATCTTA	84708
rs925664	snp	A/C	0.00835141	0.0640778	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519046	ATGAGGCATGCAGCA[A/C]TGATAAATGGCCCTG	84708
rs932038	snp	A/G	0.0267878	0.112589	intron-variant	LNX1	GRCh38.p7	4:53585079	TTCACTTCCAGGTAC[A/G]GGTTTTCAAAGGGAC	84708
rs932039	snp	A/G	0.220843	0.248294	intron-variant	LNX1	GRCh38.p7	4:53585008	CCATCTGGACTACCC[A/G]GGAAGACAATTGGAA	84708
rs932040	snp	A/T	0.35574	0.226537	intron-variant	LNX1	GRCh38.p7	4:53582727	GCATCATCAACAATT[A/T]AAAAAAAAACAAAAA	84708
rs959094	snp	C/T	0.460813	0.134379	intron-variant	LNX1	GRCh38.p7	4:53617402	TCCCAAAGTAAATTT[C/T]CTTTTCTGGATATTA	84708
rs967018	snp	A/G	0.128632	0.218563	intron-variant	LNX1	GRCh38.p7	4:53478244	TCTAAGTGGTTCTTT[A/G]GTGGGTTGATCCGGT	84708
rs979006	snp	A/G	0.247905	0.249991	intron-variant	LNX1	GRCh38.p7	4:53586711	AAGAAGGGCAAAGGC[A/G]AAGAGAACAAGAGTA	84708
rs1002824	snp	A/C	0.391769	0.205917	intron-variant	LNX1	GRCh38.p7	4:53579813	AGTTGCCAGAATAAA[A/C]CACATACTCCACTAG	84708
rs1013928	snp	A/C	0.499784	0.0103811	intron-variant	LNX1	GRCh38.p7	4:53649344	GTCAATCCCACAAGG[A/C]GACTACTATTACAAT	84708
rs1014056	snp	C/T	0.337841	0.23406	intron-variant, utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53459823	TCTTAAGAGGCTGCA[C/T]CACAAAAGGCAACAA	84708
rs1015801	snp	A/G	0.240478	0.249819	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595381	AGTCAACAGGCATGT[A/G]AGGACATGAAGCAGT	84708
rs1022187	snp	C/G	0.306431	0.243548	intron-variant	LNX1	GRCh38.p7	4:53651408	TGGGCATTGAATTCA[C/G]TTCAACAAATGTCGA	84708
rs1028000	snp	C/T	0.354665	0.227036	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594364	GGTCATTTTTCTCTG[C/T]AACTTCTGCGGCCTA	84708
rs1036379	snp	A/G	0.117188	0.211804	intron-variant	LNX1	GRCh38.p7	4:53553659	CATGGAGGTCTGCGG[A/G]TGAGGGCATGTGGGG	84708
rs1040084	snp	A/G	0.361684	0.223667	intron-variant	LNX1	GRCh38.p7	4:53544057	GTCTTCTTCACCTTC[A/G]CTGTCCTATTTTTGA	84708
rs1077966	snp	C/T	0.251296	0.249997	intron-variant	LNX1	GRCh38.p7	4:53651174	TGGACTTGGTGTAAG[C/T]AAATGTTCACTCAAC	84708
rs1125349	snp	A/G	0.499776	0.0105807	intron-variant	LNX1	GRCh38.p7	4:53649343	TGTCAATCCCACAAG[A/G]CGACTACTATTACAA	84708
rs1126328	snp	C/T	0.268452	0.249318	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595556	TTAGGAGCAAGCCTC[C/T]TTTGCAGTCAACATA	84708
rs1212751	snp	A/G	0	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510973	AGATTATGCCATTAA[A/G]AAACCATTGCACTTT	84708
rs1347406	snp	A/G	0.402277	0.198272	intron-variant	LNX1	GRCh38.p7	4:53586320	CACGTGACTGTCAAA[A/G]GCAGTCATAAGCAAG	84708
rs1369351	snp	C/T	0.269267	0.249256	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596785	CATCCCTGACTTCCC[C/T]CTATTATAATGACAA	84708
rs1369352	snp	C/G	0.370772	0.218893	intron-variant	LNX1	GRCh38.p7	4:53530885	TGAGTCACTATGCCT[C/G]GCCTCATTTTACAAT	84708
rs1369353	snp	A/G	0.447032	0.153878	intron-variant	LNX1	GRCh38.p7	4:53530794	TGTAATTTGACCCTG[A/G]AATACTTAAACAAAA	84708
rs1369354	snp	A/C	0.403334	0.197456	intron-variant	LNX1	GRCh38.p7	4:53581807	ATCAAAAACAAGATG[A/C]GTGATATGGTTTGGC	84708
rs1369355	snp	C/T	0.402806	0.197864	intron-variant	LNX1	GRCh38.p7	4:53580693	CACCTAATGCCACTA[C/T]ATATTTTTGCATTTT	84708
rs1398157	snp	A/C	0.0209421	0.100162	intron-variant	LNX1	GRCh38.p7	4:53524716	TTTAGGGGAAATAAA[A/C]ATAGTTGAGCCATTT	84708
rs1398158	snp	A/G	0.0912534	0.193131	intron-variant	LNX1	GRCh38.p7	4:53526202	AAACCCCATCACTGG[A/G]CACGGCACACTGCTC	84708
rs1399241	snp	C/T	0.455977	0.141681	intron-variant	LNX1	GRCh38.p7	4:53483140	ATCTCGAGAACAGCA[C/T]GGGAAAGACCCACCC	84708
rs1435210	snp	C/T	0.0869089	0.189476	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513277	ATGTATTATGCTTTA[C/T]GGATGTGGTCTCATT	84708
rs1435211	snp	A/G	0.275464	0.2487	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513278	TGTATTATGCTTTAT[A/G]GATGTGGTCTCATTT	84708
rs1435212	snp	C/G	0.0894459	0.191631	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513353	ATGAAGATATGGACA[C/G]TAGAAGGGAGAAATG	84708
rs1435213	snp	A/C	0.0955749	0.196603	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514905	GAACATTTAACTGAC[A/C]AATTAGGCTAAACAT	84708
rs1435214	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53590733	TGTAACCAAAGGTCA[A/G]CAGGCAGCCAGTCCA	84708
rs1435215	snp	C/T	0.334871	0.235153	intron-variant	LNX1	GRCh38.p7	4:53545367	TTCACACCTTTATAA[C/T]TCAGTAGGGCCAGGT	84708
rs1435216	snp	C/T	0.0275645	0.114116	intron-variant	LNX1	GRCh38.p7	4:53545221	TCCTAGTTTGTATAA[C/T]TATTTTCCCATTGAA	84708
rs1435217	snp	C/T	0.0275645	0.114116	intron-variant	LNX1	GRCh38.p7	4:53545210	ATAACTATTTTCCCA[C/T]TGAAGTAGGCATAAG	84708
rs1435218	snp	A/G	0.159951	0.233219	intron-variant	LNX1	GRCh38.p7	4:53535732	GCAGGGAATAGACTA[A/G]GAAGTACATGGCATA	84708
rs1435219	snp	C/T	0.45692	0.1403	intron-variant	LNX1	GRCh38.p7	4:53535682	AGCCAAGAAACTCAA[C/T]TCATTTCCCTGGCTC	84708
rs1435220	snp	A/G	0.333952	0.235483	intron-variant	LNX1	GRCh38.p7	4:53535586	ACATTTACCTCTGAG[A/G]ACATTAATGCAGAGT	84708
rs1435221	snp	C/T	0.44651	0.154543	intron-variant	LNX1	GRCh38.p7	4:53532609	GAGGAGAATTTCCTA[C/T]GGGGACTATCAAAAT	84708
rs1435222	snp	A/G	0.489492	0.0717183	intron-variant	LNX1	GRCh38.p7	4:53530223	TGTATATTTTAAAAC[A/G]TTACTTAAAAATAAT	84708
rs1435223	snp	A/T	0.31503	0.241394	intron-variant	LNX1	GRCh38.p7	4:53530046	TAATTTTTACTTGAT[A/T]AAACATATCAAACTT	84708
rs1435224	snp	C/T	0.0901694	0.192235	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510076	GACAAGCAAATGTTT[C/T]ATCTGCTTAGAAAGA	84708
rs1435225	snp	C/T	0.380333	0.213338	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577610	CTGGTCAACATAGCA[C/T]GACCCCATCTTTAAA	84708
rs1464028	snp	A/C	0.406814	0.194704	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594657	TAGCAGTTGGTTTTA[A/C]CCCCCAAGATCAAAC	84708
rs1467156	snp	G/T	0.497121	0.0378299	intron-variant	LNX1	GRCh38.p7	4:53472685	gtttttttttttttt[G/T]ttgttgttgttgttg	84708
rs1477873	snp	A/C	0.0532157	0.154195	intron-variant	LNX1	GRCh38.p7	4:53644659	AGTCACCTGACATGG[A/C]ATCCCGCTCCCTCCT	84708
rs1477875	snp	A/G	0.302435	0.244439	intron-variant	LNX1	GRCh38.p7	4:53626338	GGTTGCATAACCCTC[A/G]TATAATAAATATACT	84708
rs1477876	snp	C/T	0.279195	0.248289	intron-variant	LNX1	GRCh38.p7	4:53616053	AGAGTCTTGGAAGGA[C/T]GGGGGTGGTGAGGAG	84708
rs1514387	snp	A/C	0.126909	0.217598	intron-variant	LNX1	GRCh38.p7	4:53483865	ATAGCAGGCAGGAAG[A/C]AAATATCTCCACCAC	84708
rs1514388	snp	A/C	0.126909	0.217598	intron-variant	LNX1	GRCh38.p7	4:53483851	GAAAATATCTCCACC[A/C]CCATTGTCTGAGTCA	84708
rs1514389	snp	C/G	0.128288	0.218372	intron-variant	LNX1	GRCh38.p7	4:53483832	TTGTCTGAGTCAATG[C/G]AAAAGAGCATGGAAT	84708
rs1541967	snp	G/T	0.468949	0.12067	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515952	ATTTACCATGAGGTT[G/T]AAAGATTCGCACAAA	84708
rs1546526	snp	A/G	0.293551	0.246177	intron-variant	LNX1	GRCh38.p7	4:53633084	GATTTAAGCAGCTAA[A/G]AAGTGATGATGTTGG	84708
rs1546527	snp	C/G	0.445855	0.155373	intron-variant	LNX1	GRCh38.p7	4:53631120	CTTAACTCCATGGGC[C/G]ACTTCCTCCTCCTCT	84708
rs1567654	snp	A/G	0.421209	0.182174	intron-variant	LNX1	GRCh38.p7	4:53582010	AAAATTTAAGGTGCA[A/G]AAAAATTCAGTAATC	84708
rs1812717	snp	C/T	0.474634	0.109726	intron-variant	LNX1	GRCh38.p7	4:53526887	AAACATCGTGAGCCT[C/T]CTGTGGAGCCAGCTG	84708
rs1858389	snp	A/C	0.0908922	0.192833	intron-variant	LNX1	GRCh38.p7	4:53524782	CAGTAGCTGGATGTT[A/C]AATTCCTCAGTTCCT	84708
rs1865509	snp	C/T	0.0887219	0.191022	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512976	CCAACTCCATCTCCA[C/T]GGCCAAACCCTGGAG	84708
rs1865510	snp	A/G	0.208779	0.246578	intron-variant	LNX1	GRCh38.p7	4:53488659	TCCAAAAACTCAATC[A/G]ATTCCTGTCTTTACC	84708
rs1903827	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53634600	TTTCCTCTGGGAGTA[C/T]CATCTCTACTGGTGG	84708
rs1913484	snp	A/G	0.43978	0.162738	intron-variant	LNX1	GRCh38.p7	4:53544157	TTGAGAGCAGTACAT[A/G]GAAATTAGTAAGCAC	84708
rs1913485	snp	A/G	0.43655	0.16643	intron-variant	LNX1	GRCh38.p7	4:53544264	CAGTGGTGCCATCTC[A/G]GCTCACTGCAGCCTC	84708
rs1913486	snp	A/C	0.327445	0.237702	intron-variant	LNX1	GRCh38.p7	4:53544426	TCTCAAACTACTGAA[A/C]TCAGGTGATCCACCC	84708
rs1965112	snp	A/G	0.349452	0.229367	intron-variant	LNX1	GRCh38.p7	4:53620628	GAAATCCGGGACTTC[A/G]GTGCATCCATCAGTG	84708
rs1972815	snp	A/G	0.324382	0.238678	intron-variant	LNX1	GRCh38.p7	4:53620367	gatcccactcccagc[A/G]tttgtaattctttac	84708
rs1978767	snp	A/G	0.334182	0.235401	intron-variant	LNX1	GRCh38.p7	4:53534601	agactagagtacagt[A/G]gtgtgaccatagctc	84708
rs1991972	snp	A/C	0.487113	0.0792303	intron-variant	LNX1	GRCh38.p7	4:53636286	ACAAAACTTCATTGT[A/C]TTGAAAAAATTAGCA	84708
rs1991973	snp	A/G	0.499295	0.0187567	intron-variant	LNX1	GRCh38.p7	4:53636319	CACCTCCTTCCACAC[A/G]TCACTGTGGTAAGAA	84708
rs1996005	snp	A/T	0.294576	0.245994	intron-variant	LNX1	GRCh38.p7	4:53640828	AACCTCTTGTGAGAA[A/T]TAGTCAATGCACAAT	84708
rs2033618	snp	A/G	0.00478085	0.0486577	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602631	TTACACGTGGTGACT[A/G]AACTAATGAAGTAGC	84708
rs2048511	snp	C/T	0.283684	0.24772	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595776	GATCCCCCCATGAAG[C/T]TTGGCGTTCTCAAGG	84708
rs2048709	snp	C/T	0.338363	0.233863	intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460228	GCATGAGTTTTTATA[C/T]AGTTACTAACGATTG	84708
rs2048710	snp	A/G	0.363985	0.222503	intron-variant	LNX1	GRCh38.p7	4:53540466	CTTGTAAGAAAGCTT[A/G]TTAAAAATAAGTGTT	84708
rs2082768	snp	A/G	0.0391387	0.134304	intron-variant	LNX1	GRCh38.p7	4:53564544	aataattattcccca[A/G]agatgtccagctcct	84708
rs2082769	snp	C/T	0.0391387	0.134304	intron-variant	LNX1	GRCh38.p7	4:53564548	attattccccagaga[C/T]gtccagctcctaatc	84708
rs2099452	snp	C/T	0.227959	0.249026	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592914	GCCGGCTCTGGTGCT[C/T]GACCTCAGGGGAGCT	84708
rs2099453	snp	C/T	0.494855	0.0504572	intron-variant	LNX1	GRCh38.p7	4:53564319	ACAGAGTTCCAACAG[C/T]CACCTGCTAGCCCTT	84708
rs2117596	snp	A/G	0.0898077	0.191933	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511450	ACTAAGTACTCTCAG[A/G]TGGTGATGGGTGATG	84708
rs2117597	snp	A/G	0.0894459	0.191631	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511521	CCCTTTTCAACCAAA[A/G]CACAAGCTTTGGAGG	84708
rs2117598	snp	A/C	0.0894459	0.191631	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511808	TTCTGATAGGGTATC[A/C]TCTGCAAAGGTCACC	84708
rs2117599	snp	A/G	0.478271	0.101943	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599120	TGGCATGTGAACCAG[A/G]GCAATTCATCTTGAA	84708
rs2117600	snp	A/G	0.487432	0.0782705	intron-variant	LNX1	GRCh38.p7	4:53551507	GTATATGAATCCTCA[A/G]CTGATAAGGAGAAAA	84708
rs2117601	snp	A/G	0.43309	0.17023	intron-variant	LNX1	GRCh38.p7	4:53551705	aaggtcaaaccaccc[A/G]gctgatctcaagtca	84708
rs2137896	snp	C/G	0.0505692	0.150756	intron-variant	LNX1	GRCh38.p7	4:53482600	tgattttccattcct[C/G]tgttacttcacttaa	84708
rs2164265	snp	A/G	0.275464	0.2487	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511373	AGGACAAGAACATAC[A/G]GTAAACCCTGGGTTG	84708
rs2164266	snp	G/T	0.288646	0.246995	intron-variant	LNX1	GRCh38.p7	4:53630096	ATTAAAAAAAGGTGG[G/T]GGGGGCATGCGGGTG	84708
rs2164267	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53636590	GTGTCAAAACAGTTA[C/T]ACAAAATGACCAGCA	84708

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