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
rs13828	snp	C/T	0	0	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615739	AATTTCAACGCGTTC[C/T]ATGAACGCTTATCAG	9972
rs727557	snp	G/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17663342	tcacagttcacttta[G/T]cctcgaactcctggg	9972
rs942467	snp	A/G	0.0838651	0.186813	synonymous-codon	NUP153	GRCh38.p7	6:17629385	TATAGACCCAGAATC[A/G]GATGACACACCTATT	9972
rs942468	snp	C/T	0.0345262	0.126772	intron-variant	NUP153	GRCh38.p7	6:17641859	ttctttttctttctt[C/T]tttttttctgagaca	9972
rs942469	snp	C/T	0.00517822	0.0506191	intron-variant	NUP153	GRCh38.p7	6:17638479	CTAGGCTGGATTATT[C/T]TGTGGAACTAGAAAA	9972
rs1006066	snp	C/G	0.172674	0.237741	intron-variant	NUP153	GRCh38.p7	6:17679884	ttcctgaggtggact[C/G]tctgcaaccttggtt	9972
rs1065057	snp	C/T	0.431863	0.17154	synonymous-codon	NUP153	GRCh38.p7	6:17688567	ATTGTGCCAGGGTGG[C/T]TACAAAGATACTTCA	9972
rs1535816	snp	C/T	0.0275645	0.114116	intron-variant	NUP153	GRCh38.p7	6:17702841	TATTACCCTTATAAC[C/T]CTTCAGTTATTTGAG	9972
rs1830818	snp	A/C	0.164873	0.23506	intron-variant	NUP153	GRCh38.p7	6:17623829	TTTCTAGGGATGCAT[A/C]TATTAGCCAATAAAT	9972
rs1854009	snp	A/G	0.0729998	0.176553	intron-variant	NUP153	GRCh38.p7	6:17677090	CCTTAAAAATAAGGA[A/G]TAAGTATATAACTAA	9972
rs1886327	snp	A/G	0.0275645	0.114116	intron-variant	NUP153	GRCh38.p7	6:17634858	gattggaccaccccC[A/G]CCTCCCCTGCTGATA	9972
rs1886328	snp	A/C	0.301681	0.2446	intron-variant	NUP153	GRCh38.p7	6:17634792	GGAATGGAGGACATA[A/C]AATTAAAGACGTTGA	9972
rs1969915	snp	A/G	0.163564	0.234582	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704174	CTCCAGAGTAGCTGG[A/G]ACTACAGGCGCCCGC	9972
rs2006705	snp	C/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17678046	taataagattgcttc[C/T]aatgtttcaccatta	9972
rs2009377	snp	C/T	0.376791	0.215463	intron-variant	NUP153	GRCh38.p7	6:17641270	GCCAGGCACGGGGGC[C/T]CGTGCCTGTAATCCC	9972
rs2057539	snp	C/T	0.172028	0.23753	intron-variant	NUP153	GRCh38.p7	6:17703413	GCGCCAGACCTCTCA[C/T]TGTTTCTTACTCCAA	9972
rs2228375	snp	A/G	0.368983	0.21987	missense	NUP153	GRCh38.p7	6:17675015	CTTGGGAATTCTTCA[A/G]TCCTTAAAACCAGTC	9972
rs2228376	snp	A/C	0.0142229	0.0831214	synonymous-codon, intron-variant	NUP153	GRCh38.p7	6:17639985	TCCTTTTAGACCTGC[A/C]GAAATCCTGAAAGAA	9972
rs2228377	snp	A/C	0.00287128	0.0377809	missense, intron-variant	NUP153	GRCh38.p7	6:17639956	AAGGAAGTGTTCTAG[A/C]TATTCTGAAAAGCCC	9972
rs2228378	snp	C/T	0.0125264	0.0781428	synonymous-codon	NUP153	GRCh38.p7	6:17628941	ATTCTCTTTTGGCAA[C/T]GTGGAGCCTGCCTCT	9972
rs2228379	snp	A/G	0.012541	0.0781871	missense	NUP153	GRCh38.p7	6:17624573	TTTGGCTCTGGAACA[A/G]CTCCTAATTCTAGTA	9972
rs2229508	snp	A/T	0.0188505	0.095236	synonymous-codon, intron-variant	NUP153	GRCh38.p7	6:17639958	AGAAGGAAGTGTTCT[A/T]GATATTCTGAAAAGC	9972
rs2229509	snp	C/T	0.0293737	0.117576	synonymous-codon	NUP153	GRCh38.p7	6:17637727	TGCTGCTCAGCCCAC[C/T]GCAACAAGCCCAGTA	9972
rs2274136	snp	C/T	0.330221	0.23678	missense, utr-variant-3-prime, intron-variant	NUP153	GRCh38.p7	6:17632830	TGCTGCTACTTGAAG[C/T]AGGTACTGAACTTCC	9972
rs2328133	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17642380	TCAGTAACAAAAAGA[A/C]AAACTGTTCAATGGG	9972
rs2328134	snp	C/T	0.0275645	0.114116	intron-variant	NUP153	GRCh38.p7	6:17694223	gtggtatgtgatcag[C/T]aagtattgattgaat	9972
rs2328135	snp	C/T			upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17707097	ACGGGGAAGGAGATC[C/T]CCGGGGCGCCGCAGA	9972
rs2876454	snp	A/G	0.117188	0.211804	intron-variant	NUP153	GRCh38.p7	6:17651676	caaagtagatttcaa[A/G]acaaaaaatatttcc	9972
rs3076077	in-del	-/CT	0	0	intron-variant	NUP153	GRCh38.p7	6:17641844	AGACAGAGCGAGACT[-/CT]GTCTCAGAAAAAAAG	9972
rs3076080	snp	C/T	0.438526	0.164189	intron-variant	NUP153	GRCh38.p7	6:17663260	acacacacacacaca[C/T]aTATATATATATATA	9972
rs3777711	snp	C/T	0.167809	0.236103	utr-variant-3-prime	NUP153	GRCh38.p7	6:17616025	CAGATAACCCCAGCA[C/T]AAAGTACAATCCAGT	9972
rs3777712	snp	C/T	0.498415	0.0281103	intron-variant	NUP153	GRCh38.p7	6:17616325	ATACATTTTCTGCTA[C/T]ACCTAACACACACGC	9972
rs3777713	snp	C/G	0.303187	0.244277	intron-variant	NUP153	GRCh38.p7	6:17650089	tccacttgtgctaaa[C/G]gcagagtagcttcta	9972
rs3777714	snp	C/T	0.172997	0.237846	intron-variant	NUP153	GRCh38.p7	6:17650215	GGATGGGAGAGGACA[C/T]TTGGAAAATGGGAAG	9972
rs3777715	snp	G/T	0.225005	0.248747	intron-variant	NUP153	GRCh38.p7	6:17676970	ACTAGACAGTGTACC[G/T]TGCTAGGGGAAAAAA	9972
rs3836949	in-del	-/G	0.498392	0.028309	intron-variant	NUP153	GRCh38.p7	6:17616282	GTCGGGTGGGGGGGG[-/G]AGTAGACTCACATTG	9972
rs4052817	in-del	-/TG/TGT	0	0	intron-variant	NUP153	GRCh38.p7	6:17649575	ATATACTACAGTTGT[-/TG/TGT]ACTAATATGAAACAT	9972
rs4142294	snp	C/T	0.259674	0.249813	intron-variant	NUP153	GRCh38.p7	6:17665574	ATTCATATACCTATG[C/T]ACATAAATATACACA	9972
rs4142295	snp	A/G	0.499673	0.0127754	intron-variant	NUP153	GRCh38.p7	6:17665656	AATGACTTTTCACAC[A/G]CATGCATGCATACAA	9972
rs4236171	snp	C/T	0.0345262	0.126772	intron-variant	NUP153	GRCh38.p7	6:17638934	GAAAAATTGAATCCT[C/T]CTAAATCCTGTTGTA	9972
rs4236172	snp	C/G	0.318174	0.240525	intron-variant	NUP153	GRCh38.p7	6:17639232	ACAGGTGCATGCCAG[C/G]ACGCCCAGCTAATTT	9972
rs4367384	snp	C/G	0.302686	0.244385	intron-variant	NUP153	GRCh38.p7	6:17667404	GAGGAACTTGGTATT[C/G]CAAGAAATGTTTTCA	9972
rs4370366	snp	A/C/T	0.0391387	0.134304	intron-variant	NUP153	GRCh38.p7	6:17646293	GCTCACTGCAACCTC[A/C/T]GCCTCCCGGGTTCAC	9972
rs4579347	snp	A/G	0.0410537	0.137264	intron-variant	NUP153	GRCh38.p7	6:17680053	catgtcaattcctgc[A/G]ctttgcctaataaaa	9972
rs4613811	snp	C/T	0.225005	0.248747	intron-variant	NUP153	GRCh38.p7	6:17666390	cgtggtggcatgcgc[C/T]tgtaatcccggctat	9972
rs4712307	snp	A/G	0.00557542	0.0525036	intron-variant	NUP153	GRCh38.p7	6:17686697	AAGTTAAGAAAAAAA[A/G]ACAGTACTATAGAAA	9972
rs4716165	snp	A/C	0.318896	0.240319	intron-variant	NUP153	GRCh38.p7	6:17618292	gtcctacactcataa[A/C]aactacaggtagcca	9972
rs4716166	snp	A/G	0.226484	0.248892	intron-variant	NUP153	GRCh38.p7	6:17623802	TTTATATAAAAGCAG[A/G]CAAAACTACATTTTC	9972
rs4716167	snp	C/T	0.497959	0.0318836	intron-variant	NUP153	GRCh38.p7	6:17627359	GCTCATAGCTATTTG[C/T]TGAATTCCATACTTT	9972
rs4716168	snp	C/T	0.303187	0.244277	intron-variant	NUP153	GRCh38.p7	6:17643229	tgtaatcccagcact[C/T]tgagacgcctaggcg	9972
rs4716169	snp	A/T	0.498611	0.0263212	intron-variant	NUP153	GRCh38.p7	6:17652574	aatattagaaaaaaa[A/T]atccagtcttcataa	9972
rs4716170	snp	A/G	0.0345262	0.126772	intron-variant	NUP153	GRCh38.p7	6:17653583	aataaatttatttac[A/G]aaaagacctgaacaa	9972
rs4716171	snp	A/G	0.0345262	0.126772	intron-variant	NUP153	GRCh38.p7	6:17653688	gaacaagtgaaacca[A/G]tacatggtggaaaaa	9972
rs4716172	snp	A/G	0.00795532	0.062565	intron-variant	NUP153	GRCh38.p7	6:17661512	TTAGGTTTTCAGCAT[A/G]CATTTTGAAAGAACT	9972
rs4716173	snp	C/T	0.499673	0.0127754	intron-variant	NUP153	GRCh38.p7	6:17670865	gcccaggctggagtg[C/T]ggtggcacaatctcg	9972
rs4716174	snp	A/G	0.499683	0.0125759	intron-variant	NUP153	GRCh38.p7	6:17670958	tgggattacaggcac[A/G]tccaactgcaaccgg	9972
rs4716175	snp	C/G	0.0341408	0.126114	intron-variant	NUP153	GRCh38.p7	6:17700027	TCATCACAAACAAAA[C/G]ACCTACTTTGCATTA	9972
rs6459561	snp	C/T	0.316968	0.240864	intron-variant	NUP153	GRCh38.p7	6:17657420	aaaaaaaaaaatagc[C/T]agccttggtggtgca	9972
rs6899967	snp	C/T	0.329317	0.237084	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708584	caatctcaggtgatc[C/T]gcccacggcctccca	9972
rs6901119	snp	C/T	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17671825	ccagcctggccaaca[C/T]ggtaaaaccctgtct	9972
rs6905654	snp	A/G	0.00693259	0.0584657	missense	NUP153	GRCh38.p7	6:17637155	GCCAAAAACATACCT[A/G]GTTTCTCAGACATAC	9972
rs6906499	snp	C/G	0.405507	0.195748	missense	NUP153	GRCh38.p7	6:17665248	ACTCACACTGCACTT[C/G]TTATCTATTCTTTGA	9972
rs6913539	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17657394	ctaaaataaaaaaat[A/T]aaaaaataaaaaaaa	9972
rs6913856	snp	A/G	0.0345262	0.126772	intron-variant	NUP153	GRCh38.p7	6:17691175	GGAAAGGTATAGGTA[A/G]CAACTGGGAAGCATG	9972
rs6913935	snp	G/T	0.499642	0.0133738	intron-variant	NUP153	GRCh38.p7	6:17644214	CTTTTGAGGATCTAG[G/T]TTTTAAAAATTCCCA	9972
rs6914067	snp	C/T	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17666429	ctgaggcaggagaat[C/T]gtttgaacccggagg	9972
rs6914251	snp	A/C	0.0244538	0.107838	intron-variant	NUP153	GRCh38.p7	6:17690708	ATGACTCAGTAGGTA[A/C]AGAAAACAATAAAAT	9972
rs6917438	snp	A/G	0.227369	0.248974	intron-variant	NUP153	GRCh38.p7	6:17631738	ttgggaggccgaggc[A/G]ggtggatcacgaagt	9972
rs6918123	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17657393	actaaaataaaaaaa[A/T]aaaaaaataaaaaaa	9972
rs6919027	snp	C/T	0.0197687	0.0974348	intron-variant	NUP153	GRCh38.p7	6:17696943	ctggcaggtggtgtc[C/T]gcctgtaatcccagc	9972
rs6919957	snp	C/T	0.172028	0.23753	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632434	AATTTTTTTTCCCAC[C/T]TGGAGAAAAGATACC	9972
rs6926424	snp	C/T	0.0345262	0.126772	intron-variant	NUP153	GRCh38.p7	6:17646407	gagatggggtttcac[C/T]gtgttagccaggatg	9972
rs6927877	snp	A/C	0.226779	0.248919	intron-variant	NUP153	GRCh38.p7	6:17647415	accaacagaaataaa[A/C]cagcaattaaaggac	9972
rs6928465	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17664369	tttaaataggagaat[A/T]gtatgatatgtgaat	9972
rs6929659	snp	A/G	0.499502	0.0157669	intron-variant	NUP153	GRCh38.p7	6:17665126	CATCACTAATTCACA[A/G]CCTTTATGTGTTATA	9972
rs6930231	snp	C/T	0.225301	0.248777	intron-variant	NUP153	GRCh38.p7	6:17682172	tgcatacaaaagtta[C/T]gtttacactacacta	9972
rs6933829	snp	A/C	0.226484	0.248892	intron-variant	NUP153	GRCh38.p7	6:17622141	CAGTTATGCTGCTAC[A/C]CAGAGTCAAGAGTTT	9972
rs6935037	snp	A/G	0.330714	0.236612	intron-variant	NUP153	GRCh38.p7	6:17665771	tgtcacccagaccac[A/G]gctcactgtaggtga	9972
rs6936033	snp	C/T	0.165853	0.235413	intron-variant	NUP153	GRCh38.p7	6:17682977	caagaagcaactcct[C/T]atccattcgagtttg	9972
rs6936057	snp	A/G	0.00517822	0.0506191	intron-variant	NUP153	GRCh38.p7	6:17662616	gaaaagaatataatt[A/G]ggaagtttccttccc	9972
rs6936505	snp	A/G	0.227074	0.248947	intron-variant	NUP153	GRCh38.p7	6:17635191	ctcggctcactgcaa[A/G]ctccacctcccagat	9972
rs6938643	snp	C/T	0.465263	0.127129	intron-variant	NUP153	GRCh38.p7	6:17663258	acacacacacacaca[C/T]acaTATATATATATA	9972
rs6938802	snp	C/G	0.195526	0.243993	intron-variant	NUP153	GRCh38.p7	6:17688193	ACATCAGAGCTTGCA[C/G]TCTTAACTGATATAG	9972
rs6939367	snp	C/T	0.0205511	0.0992634	intron-variant	NUP153	GRCh38.p7	6:17665554	TAATGGAACCTAAGG[C/T]ATGTATTCATATACC	9972
rs7739638	snp	A/G	0.0248432	0.108648	intron-variant	NUP153	GRCh38.p7	6:17658648	ggtcattcaccattt[A/G]aagaaaattggaaag	9972
rs7740055	snp	C/T	0.331642	0.236293	intron-variant	NUP153	GRCh38.p7	6:17664179	tgaaccttgaaaaca[C/T]tatgctaagtgGCTA	9972
rs7740061	snp	C/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17672065	tagaaacaagccaat[C/T]ttagatttttataga	9972
rs7740284	snp	A/G			downstream-variant-500B	NUP153	GRCh38.p7	6:17614649	ctggggggggggggg[A/G]gtgcagttctgggaa	9972
rs7742319	snp	A/G	0.0452528	0.143452	upstream-variant-2KB, nc-transcript-variant, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707237	TGGTTAAGTAGGCAG[A/G]AAGTAAGCAGACAGT	9972
rs7742356	snp	A/G	0.17332	0.23795	upstream-variant-2KB, nc-transcript-variant, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707304	GAAAAAAAAATCTGT[A/G]GTTGAAAAATAAAGT	9972
rs7742489	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17667731	aaaaagaaaagaaaa[A/G]aaagaaaaaTCCAAC	9972
rs7743000	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17668047	AGATGATGATGTGCA[A/G]TGAGGACTTTAGTTT	9972
rs7745019	snp	A/G	0.172351	0.237636	intron-variant	NUP153	GRCh38.p7	6:17656084	GTGGCGTACGCTTGT[A/G]ATCCCAGCTACTCAG	9972
rs7745148	snp	A/T	0.00835141	0.0640778	intron-variant	NUP153	GRCh38.p7	6:17680073	gcctaataaaaaaaa[A/T]tcctactggcttttt	9972
rs7745349	snp	A/T	0.26518	0.249539	intron-variant	NUP153	GRCh38.p7	6:17686329	agaaagccatgatat[A/T]gctgatactgacttt	9972
rs7747119	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17668062	ATGAGGACTTTAGTT[C/T]ACTGAACtttttttt	9972
rs7754076	snp	A/G	0.0345262	0.126772	intron-variant	NUP153	GRCh38.p7	6:17693105	CCATGATTTTCACCT[A/G]TACTGTTTTTCTCTG	9972
rs7754546	snp	A/G	0.0248432	0.108648	intron-variant	NUP153	GRCh38.p7	6:17663233	TAAAAAGAAAAAAAT[A/G]cacacacacacacac	9972
rs7755660	snp	A/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17657948	attttatattatttt[A/G]gactgtggaaatgat	9972
rs7757195	snp	C/T	0.225005	0.248747	intron-variant	NUP153	GRCh38.p7	6:17684568	tgctttcatattatc[C/T]tttgtgtgtttacta	9972

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