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
rs1745	snp	A/G	0.423881	0.179625	utr-variant-3-prime	TMF1	GRCh38.p7	3:69021306	TTCACTGGGGGTCTT[A/G]GAACGTATGTCCCAT	7110
rs15780	snp	A/C	0.449091	0.151204	utr-variant-3-prime	TMF1	GRCh38.p7	3:69021248	TATATGTATAGGAAA[A/C]AACAGTGTATAGAGG	7110
rs937858	snp	A/C	0.40108	0.199185	intron-variant	TMF1	GRCh38.p7	3:69033722	CATTGGTAATGACTT[A/C]AGAATTTCATGATTC	7110
rs937859	snp	A/G	0.454295	0.144096	intron-variant	TMF1	GRCh38.p7	3:69033506	TGCAGAAGCTCTTCC[A/G]TCTTGTTTATAGAAT	7110
rs1044302	snp	A/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69020190	ATGTTCAGGAAATTT[A/T]TTTTCTCCATCTCTT	7110
rs1053555	snp	G/T	0.480931	0.0957637	utr-variant-3-prime	TMF1	GRCh38.p7	3:69021412	GTCAGCTTGATTTTT[G/T]TGTGTGTGTAATATT	7110
rs1246013	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69042047	ttattttatttattt[A/T]tttttttgatacaaa	7110
rs1344931	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69033286	ATTCAGTTCTTTTTT[A/T]TTTTTTTTTTTGATA	7110
rs1463957	snp	A/G	0.470618	0.117591	intron-variant	TMF1	GRCh38.p7	3:69044846	TAGATCCCCAACTAG[A/G]TATTGCCTAATTGTT	7110
rs1532918	snp	C/G	0.190055	0.242717	missense	TMF1	GRCh38.p7	3:69033557	GAGAAGAATCTTTCT[C/G]ATAGGCTTGGTAACT	7110
rs2055685	snp	C/G	0.45479	0.161862	intron-variant	TMF1	GRCh38.p7	3:69034911	ATTCAGCAAATGCTA[C/G]GTGTGACAGTAATCC	7110
rs2271118	snp	A/G	0.305759	0.243703	intron-variant	TMF1	GRCh38.p7	3:69044447	ACACATTTTCTGGAA[A/G]CCTGTATACTTTGTA	7110
rs2271119	snp	C/T	0.44546	0.155869	intron-variant	TMF1	GRCh38.p7	3:69044240	TTTTAGTATTAGAGA[C/T]TTAAAACGTATTTGA	7110
rs2271120	snp	A/G	0.378045	0.214719	intron-variant	TMF1	GRCh38.p7	3:69042565	CCCTGTAAAATAGAC[A/G]GAAATTTGTGCTGCC	7110
rs2271121	snp	A/C	0.41979	0.183497	intron-variant	TMF1	GRCh38.p7	3:69035010	TTTGTGTTTTGGAAA[A/C]CTGTGACAGTACCTG	7110
rs2271122	snp	C/T	0.385359	0.210185	intron-variant	TMF1	GRCh38.p7	3:69035283	TTCATCAAGCAATTC[C/T]AAAACTGTATGTATA	7110
rs2279936	snp	A/G	0.29432	0.24604	intron-variant	TMF1	GRCh38.p7	3:69025779	TCCATTACCAGGTTC[A/G]AACAAAAATGGTTCT	7110
rs2292199	snp	C/T	0.32291	0.239132	synonymous-codon	TMF1	GRCh38.p7	3:69047463	TATCTTGGTTTCTTC[C/T]ACACCAATAAATGAA	7110
rs2314230	snp	C/T	0.45946	0.136478	intron-variant	TMF1	GRCh38.p7	3:69045743	CAGGGCAAGACTCCG[C/T]CTCAAAAAATAAATA	7110
rs2314231	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69046520	AATCTGGCACTTTTT[A/T]AAAAAATTAAGTAAT	7110
rs3732628	snp	A/G	0.459914	0.13578	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049284	GAGGCTGAGGTGGGA[A/G]GATCATCTGAGCCCA	7110
rs3736422	snp	C/T	9.93772e-05	0.00704831	missense	TMF1	GRCh38.p7	3:69038670	CTCAGAGCAGCTTCC[C/T]GTGCCTCACTATCCT	7110
rs3772976	snp	A/G	0.395453	0.203331	intron-variant	TMF1	GRCh38.p7	3:69024259	ATAAAAATATTTAAT[A/G]TGTGTGTGGTTTTTT	7110
rs3772977	snp	C/T	0.178144	0.239451	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050785	CTGACTTTTCAATGA[C/T]GTAAAATTAAGAACA	7110
rs3817105	snp	A/G	0.448452	0.152042	intron-variant	TMF1	GRCh38.p7	3:69044226	ATTTAAAACGTATTT[A/G]AAGAAAACTGTGTTA	7110
rs3836333	in-del	-/ATTT			intron-variant	TMF1	GRCh38.p7	3:69024421	GAGATAAATCCAATT[-/ATTT]GTTTGAAAACATTCA	7110
rs4855351	snp	A/G	0.467337	0.123551	upstream-variant-2KB	TMF1	GRCh38.p7	3:69054106	GAACAGAAAACTGCC[A/G]TATCTAAGTCAAAAA	7110
rs4855352	snp	A/G	0.467744	0.122832	upstream-variant-2KB	TMF1	GRCh38.p7	3:69054142	AATGAGAACACATAC[A/G]TGTTCTCATATTAAA	7110
rs6549177	snp	A/G	0.0670745	0.170406	intron-variant	TMF1	GRCh38.p7	3:69037322	ACACGCTGAAACCCC[A/G]TGTCTACTAAAAATA	7110
rs6549178	snp	G/T	0.47614	0.106587	intron-variant	TMF1	GRCh38.p7	3:69042057	TATTTATTTTTTTGA[G/T]ACAAAGTCTCACTCT	7110
rs6765571	snp	A/G	0.45645	0.140991	intron-variant	TMF1	GRCh38.p7	3:69031571	tattaggcaatgtgt[A/G]caaaggacctttcta	7110
rs6767963	snp	C/T	0.00557542	0.0525036	intron-variant	TMF1	GRCh38.p7	3:69031333	aaaaagaaaaaaagc[C/T]aacaggaaggactca	7110
rs6801855	snp	C/T	0.0607341	0.163335	intron-variant	TMF1	GRCh38.p7	3:69031628	tctacattatatcaa[C/T]aaaaattttcaattg	7110
rs7375020	snp	A/G	0.487432	0.0782705	intron-variant	TMF1	GRCh38.p7	3:69024766	AAAAGAGGTATCCTG[A/G]TTCAAAATGCTTGAG	7110
rs7426611	snp	C/T	0.0123036	0.0774623	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049570	TTCTCAAATTCTAAA[C/T]TATGTCAGAAATTAC	7110
rs7429868	snp	C/T	0.0577344	0.159793	intron-variant	TMF1	GRCh38.p7	3:69030784	aaaacagggacgaca[C/T]aaaatgttggcaagg	7110
rs7612705	snp	C/T	0.0748431	0.178382	intron-variant	TMF1	GRCh38.p7	3:69025212	CTTCCCTTTATTCTG[C/T]TGGGAAAGAGCTGCT	7110
rs8179890	snp	A/G	0.0228355	0.104385	utr-variant-3-prime	TMF1	GRCh38.p7	3:69022510	GGATAGGTACCAAAA[A/G]GTACCACATTTTATA	7110
rs9809889	snp	G/T	0.488786	0.0740357	intron-variant	TMF1	GRCh38.p7	3:69038261	CAGGAGTTAAATGGA[G/T]TCTCTCAAAATTATA	7110
rs9811018	snp	C/T	0.00380945	0.0434766	synonymous-codon	TMF1	GRCh38.p7	3:69038905	AAGTTCATCCATGTC[C/T]ACCTGAAGACGGCCA	7110
rs9813514	snp	A/G	0.397271	0.202018	intron-variant	TMF1	GRCh38.p7	3:69031030	aatggttaaatatac[A/G]tggtacatactatgg	7110
rs9813815	snp	A/G	0.021333	0.101051	intron-variant	TMF1	GRCh38.p7	3:69031231	ttagtgattgccaga[A/G]atttgggacaaggga	7110
rs9826616	snp	A/C	0.405255	0.195948	intron-variant	TMF1	GRCh38.p7	3:69026621	GTAAAACTCAGTCTC[A/C]AAAACAAACAAACAA	7110
rs9855731	snp	A/G	0.254664	0.249956	intron-variant	TMF1	GRCh38.p7	3:69028046	GTAATTCATGCCATG[A/G]TAAGTCAATCTCAAA	7110
rs9862298	snp	C/T	0.487432	0.0782705	intron-variant	TMF1	GRCh38.p7	3:69023610	TAAGCACACTTGATA[C/T]AAAATTTAGTCTCTT	7110
rs9985501	snp	C/T	0.0444908	0.142359	intron-variant	TMF1	GRCh38.p7	3:69042489	TAAATCCCAGAGTTA[C/T]ACACTTTGAATGTCT	7110
rs10681795	in-del	-/T			intron-variant	TMF1	GRCh38.p7	3:69024823	TTTTTTTTTTTTTTT[-/T]CAGATTATGGAATAA	7110
rs10707788	in-del	-/G	0.468249	0.121932	downstream-variant-500B, upstream-variant-2KB	UBA3, TMF1	GRCh38.p7	3:69054291	GGGGGGCGGGGGGGG[-/G]TGGATCACCTGAGGT	7110
rs10865643	snp	A/G	0.415235	0.18761	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050595	CAAATATCCTTATAT[A/G]TAAAACCTATATTCT	7110
rs11128108	snp	C/T	0.443598	0.158176	intron-variant	TMF1	GRCh38.p7	3:69036694	TGTAAATGTTTTACA[C/T]ATACAAAACTTAAAA	7110
rs11128109	snp	C/T	0.44768	0.153045	intron-variant	TMF1	GRCh38.p7	3:69037312	ATCCTGGCTAACACG[C/T]TGAAACCCCATGTCT	7110
rs11128110	snp	A/G	0.448963	0.151372	intron-variant	TMF1	GRCh38.p7	3:69044164	TCTGAATCTTCTTGT[A/G]TCACATTTTCCCAAT	7110
rs11318005	in-del	-/A	0.488606	0.0746142	intron-variant	TMF1	GRCh38.p7	3:69027680	AATAGCTGATGAACT[-/A]AAAAAAAAAAAAAAA	7110
rs11338290	in-del	-/T	0.390277	0.206936	intron-variant	TMF1	GRCh38.p7	3:69028724	AGGAAGAACAGAGGG[-/T]TAAAAAATACTAACC	7110
rs11447014	in-del	-/T			intron-variant	TMF1	GRCh38.p7	3:69032613	TTTTTTTTTTTTTTT[-/T]GAGATGCAGTCTCGC	7110
rs11557640	snp	A/G			missense	TMF1	GRCh38.p7	3:69027959	TTAGAAATTTAAAGA[A/G]TGAAAGTTGAACAAG	7110
rs12054469	snp	C/G	0.428182	0.17536	intron-variant	TMF1	GRCh38.p7	3:69042086	CTGTCGCCCAGGCTG[C/G]AGTACAGTGGCGTGA	7110
rs12489922	snp	C/T	0.462034	0.132445	upstream-variant-2KB	TMF1	GRCh38.p7	3:69053849	ACCATCTAAAACTAT[C/T]TATTCAGCTCTCAGA	7110
rs12636843	snp	C/T	0.0372196	0.131242	downstream-variant-500B, upstream-variant-2KB	UBA3, TMF1	GRCh38.p7	3:69054241	AAAAACATggtcagg[C/T]atggtggctcatgcc	7110
rs13063094	snp	A/T	0.409891	0.192184	intron-variant	TMF1	GRCh38.p7	3:69027000	TTTATTTATTTATTT[A/T]TTTTTATTTTTTTGA	7110
rs13068103	snp	A/G/T			intron-variant	TMF1	GRCh38.p7	3:69040751	ACATGGTGAAACCCC[A/G/T]TCTCTACTAAAAATA	7110
rs13071583	snp	A/T	0.445592	0.155704	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050957	AGATCCCTGAAAGAT[A/T]AAGCTCAATGAAACT	7110
rs13073272	snp	A/G	0.487177	0.0790385	intron-variant	TMF1	GRCh38.p7	3:69034024	TTCATCATGTTGCTC[A/G]GGCTGGCCTCGAACT	7110
rs13073502	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69034166	GTTAGATTGTGTAAT[A/C]CAGTATCTAAATAAG	7110
rs13079161	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69041982	TTCAGTATCCATTTG[G/T]AATGATTTATTTCAT	7110
rs13084180	snp	A/T	0.117188	0.211804	intron-variant	TMF1	GRCh38.p7	3:69045961	ctagagcggattagg[A/T]gggaggactgcttga	7110
rs13094896	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69034445	gccactgcactcctg[C/G]ctgggcaacagagca	7110
rs13095343	snp	C/G	0	0	intron-variant	TMF1	GRCh38.p7	3:69041932	CACGTTTTCCAAAGG[C/G]TCCTCTCTCCCAGGA	7110
rs13099820	snp	A/G	0.400325	0.199756	intron-variant	TMF1	GRCh38.p7	3:69035522	GCCTTTTTGGAAAAC[A/G]TTATAATATGTTTAA	7110
rs13319158	snp	G/T	0.067446	0.170804	intron-variant	TMF1	GRCh38.p7	3:69051044	GTCACACATTTTCCG[G/T]CTAATACCTCCGGCA	7110
rs17005231	snp	C/T	0.0154538	0.0865337	intron-variant	TMF1	GRCh38.p7	3:69030105	TAATGATGCAAGTAG[C/T]CACACTTAAAACTGA	7110
rs17005239	snp	A/G	0.0217236	0.101931	intron-variant	TMF1	GRCh38.p7	3:69031898	GTACCAGTTTCTAGC[A/G]TTCATTTATTGCTAA	7110
rs17005254	snp	A/C	0.480223	0.0974544	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049788	ATAATCAGGATCTTA[A/C]AAATGGTATATTCGT	7110
rs17048274	snp	A/G	0.0431256	0.140367	intron-variant	TMF1	GRCh38.p7	3:69023330	CAAATCCTGAAAAAT[A/G]TATTTGTTTACAATT	7110
rs28372813	snp	C/T	0.0111196	0.0737302	upstream-variant-2KB, utr-variant-5-prime	TMF1	GRCh38.p7	3:69052378	CTCCCGGATGTGACG[C/T]CAACGTTCTTCTGTT	7110
rs28480268	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69028471	TCTGAGTTTCACTCA[G/T]AAACCAAACCAAAAG	7110
rs34091520	in-del	-/AC	0.344147	0.231595	intron-variant	TMF1	GRCh38.p7	3:69031417	TGTTTAGAACTTAAT[-/AC]ACACACACACACACA	7110
rs34175383	snp	A/G	0.442791	0.15916	intron-variant	TMF1	GRCh38.p7	3:69051739	ACCAAAGAAAGACAA[A/G]GGGGAACCTGGATCT	7110
rs34206158	snp	C/G/T	0.00113433	0.0237884	synonymous-codon	TMF1	GRCh38.p7	3:69047880	TGTAGTCTCTTGTCT[C/G/T]GAGCTCGCTGAGCTC	7110
rs34224196	in-del	-/T			intron-variant	TMF1	GRCh38.p7	3:69044469	AAATGTGTAACATTA[-/T]TTCACATTTGCAGAA	7110
rs34283375	in-del	-/T			intron-variant	TMF1	GRCh38.p7	3:69039713	GATGGTAAAGAAGTA[-/T]TAAACTCAAATGATA	7110
rs34428015	snp	C/T	0.0101778	0.0706068	missense	TMF1	GRCh38.p7	3:69047362	ACTAGAGTTACCTTG[C/T]AAACATCTTCCTTCT	7110
rs34504690	in-del	-/A			intron-variant	TMF1	GRCh38.p7	3:69046901	AATAATTAAAATCTT[-/A]AATTATCATTTAATA	7110
rs34547039	in-del	-/C			intron-variant	TMF1	GRCh38.p7	3:69028193	ATTCTCTAATGTATG[-/C]CCTAAGAGCTGAGTG	7110
rs34778745	in-del	-/A	0.5	0	intron-variant	TMF1	GRCh38.p7	3:69033292	GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	7110
rs34917634	snp	A/G	0.00870681	0.0654033	missense	TMF1	GRCh38.p7	3:69038653	TAGCTTTCATTTCAC[A/G]GCTCAGAGCAGCTTC	7110
rs34956334	in-del	-/AA	0.379354	0.213933	intron-variant	TMF1	GRCh38.p7	3:69046303	TGGACTCAAAAAAAT[-/AA]AGTCTTACCTGAGTT	7110
rs35069139	in-del	-/G			utr-variant-3-prime	TMF1	GRCh38.p7	3:69021973	CAGGCATGAGCCACA[-/G]GCACCTGGCCGTAAA	7110
rs35347565	in-del	-/T	0.15698	0.23205	utr-variant-3-prime	TMF1	GRCh38.p7	3:69021685	TTAAATAAGAGTTTG[-/T]TTTTTTTTTTTTTGA	7110
rs35447207	snp	C/G	0.000832237	0.020382	missense	TMF1	GRCh38.p7	3:69047417	CAGCAGGTTCACACT[C/G]CTCAGCCACCTTGTC	7110
rs35708142	in-del	-/A			intron-variant	TMF1	GRCh38.p7	3:69040432	GGGAGATGTAGACTG[-/A]AAGAATTTAGGAGCA	7110
rs35783734	snp	A/G	0.00884184	0.0658995	synonymous-codon	TMF1	GRCh38.p7	3:69023240	ATTTTTTACATCTTC[A/G]AGATCTAATCGAAGT	7110
rs35856064	snp	A/G	0.000873377	0.0208788	missense	TMF1	GRCh38.p7	3:69028261	CAAGTGTTCTTACAT[A/G]TTCATCTTTTAGGTT	7110
rs35933614	in-del	-/C			intron-variant	TMF1	GRCh38.p7	3:69027606	TCCAATCTTTTGGTT[-/C]CCCTGGGCCTCATTT	7110
rs35970969	snp	A/G	0.0256215	0.110247	intron-variant	TMF1	GRCh38.p7	3:69029540	ACTTCCGCCTCCCGG[A/G]TGTAAGCGATTCTCA	7110
rs36000302	in-del	-/A			intron-variant	TMF1	GRCh38.p7	3:69027756	TGTTGGGCTTCATTC[-/A]AAAATCATCCTGGGC	7110
rs41291189	snp	A/G	0.101282	0.200955	intron-variant	TMF1	GRCh38.p7	3:69025727	CCTATGTTAATTAAG[A/G]AAGTTCACACAGTTA	7110
rs41291191	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69029518	GGTGGGATCTTGGCT[A/C]ACTGCAACTTCCGCC	7110
rs41291193	snp	C/T	1.6563e-05	0.00287771	synonymous-codon	TMF1	GRCh38.p7	3:69035032	CAGTACCTGCTGAAG[C/T]TCACCGATCTCATGG	7110
rs41291195	snp	G/T	0.00993419	0.0697739	intron-variant	TMF1	GRCh38.p7	3:69039115	AATATATATTTTTTT[G/T]AGACAAAGTCTCGCT	7110

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