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
rs1138860	snp	C/G	0.340784	0.232934	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621736	ACTGCACTCCAGCCT[C/G]GGTGACAGAGCAAGA	55159
rs1138861	snp	A/C	0.456332	0.141164	utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621703	CCATCTCAAAAAAAA[A/C]AAACAAACAAAAAAA	55159
rs1802616	snp	A/C			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668314	AAAGAAACCATTGAC[A/C]AGAGCTGAAGTGGGA	55159
rs3202910	snp	A/C	0.161267	0.233723	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621707	GACTCCATCTCAAAA[A/C]AAACAAACAAACAAA	55159
rs3205212	snp	A/C	0	0	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623503	CCTTGAAGGGACTAA[A/C]CATCGTCTTGGTACT	55159
rs3208607	snp	C/T	0	0	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668689	ATTCTTCCTGATGAC[C/T]CTAGAAAACCCAACT	55159
rs3208608	snp	C/T	0.1128	0.208988	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668698	GATGACTCTAGAAAA[C/T]CCAACTGAATGGTAT	55159
rs3208609	snp	C/T	0.131038	0.219882	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668770	GTGTTGAAGAACATT[C/T]GTGTACGCTTTTTGA	55159
rs3208610	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668777	AGAACATTCGTGTAC[A/G]CTTTTTGACTCCAAG	55159
rs3208611	snp	G/T	0	0	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668781	CATTCGTGTACGCTT[G/T]TTGACTCCAAGAACT	55159
rs3923862	snp	C/G	0.202959	0.245534	intron-variant	RFWD3	GRCh38.p7	16:74658924	AAAAATTAGCCGGGC[C/G]TGGTGGCACACACCT	55159
rs4072450	snp	C/G	0.347914	0.230028	intron-variant	RFWD3	GRCh38.p7	16:74632736	GAGCTACTTGAAAAA[C/G]TAGTTTGAATTGCCC	55159
rs4243108	snp	C/T	0.3512	0.228601	intron-variant	RFWD3	GRCh38.p7	16:74658555	TTCAGAAGTTATAAG[C/T]GATTAGTCCTGGGAA	55159
rs4271617	snp	C/T	0.336017	0.234736	intron-variant	RFWD3	GRCh38.p7	16:74640373	ctggtctcgaacttc[C/T]gaccttgtgatccgc	55159
rs4286131	snp	C/G	0.335788	0.23482	intron-variant	RFWD3	GRCh38.p7	16:74642143	CCTTTTTAAAtttga[C/G]acagagtcttgctct	55159
rs4287593	snp	C/T	0.336017	0.234736	intron-variant	RFWD3	GRCh38.p7	16:74642652	GTGTACCACTACACA[C/T]GGATAATTTTTTTCA	55159
rs4346229	snp	C/G	0.199873	0.244923	intron-variant	RFWD3	GRCh38.p7	16:74640109	TCCTTGTGGCTAAGG[C/G]GGGACTACTGTAGCC	55159
rs4395097	snp	C/T	0.206029	0.246103	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668532	TGTTCCCTTGGCAGA[C/T]GTCAAGTGAGAAAAT	55159
rs4402594	snp	C/T	0.462909	0.131034	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667462	AATCTCAAACCGCTG[C/T]AAGGGATCTGAGCTA	55159
rs4448975	snp	A/G	0.207253	0.246318	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668356	CAGGAAAGAAGAGTA[A/G]AAAGGGATATTCTTA	55159
rs4462623	snp	C/T	0.3512	0.228601	intron-variant	RFWD3	GRCh38.p7	16:74658528	CCACACTGAGAAATT[C/T]ATCTCAAGAAATTCA	55159
rs4500770	snp	A/T	0.414245	0.188477	intron-variant	RFWD3	GRCh38.p7	16:74624532	tcccaagtagctggg[A/T]ttacagacatccacc	55159
rs4531752	snp	C/T	0.202035	0.245356	intron-variant	RFWD3	GRCh38.p7	16:74634962	GCCTGACCAAAATGT[C/T]AAAACCCCATTTCAA	55159
rs4544266	snp	A/C	0.362941	0.223034	intron-variant	RFWD3	GRCh38.p7	16:74627095	AGTCTTGGAGACAGC[A/C]GAGCTGTGGGATGAT	55159
rs4558441	snp	A/G	0.0252325	0.109451	intron-variant	RFWD3	GRCh38.p7	16:74628149	TCTCAAGGTGGCTCA[A/G]TGACCTAGAGCTGGC	55159
rs4564599	snp	C/T	0.335101	0.23507	intron-variant	RFWD3	GRCh38.p7	16:74635343	ATGGTGGCATGCACC[C/T]GTAGTCTCAACTACT	55159
rs4887780	snp	A/G	0.499946	0.00519141	downstream-variant-500B	RFWD3	GRCh38.p7	16:74620991	taaaaaaaaaaaaaa[A/G]aaaaaaggccgggtg	55159
rs4887781	snp	C/G	0.394904	0.203722	downstream-variant-500B	RFWD3	GRCh38.p7	16:74621252	ACTGCACTCCAGCTA[C/G]GGCTACAGAGCAAGA	55159
rs4887782	snp	C/T	0.00398564	0.0444627	intron-variant	RFWD3	GRCh38.p7	16:74627682	gggtacctgccagta[C/T]aaacaagtttcctgt	55159
rs4887783	snp	C/G	0.451109	0.148509	utr-variant-5-prime	RFWD3	GRCh38.p7	16:74666845	CTCGGTAGTTACCTC[C/G]GCCGCACTCCGAATG	55159
rs4888262	snp	C/T	0.494848	0.0504932	synonymous-codon	RFWD3	GRCh38.p7	16:74636560	CTGACTTTGATGTGA[C/T]GTAAGTTTTTGCAAG	55159
rs4888263	snp	A/G	0.201418	0.245234	intron-variant	RFWD3	GRCh38.p7	16:74636923	TTACCACGTTGGCCG[A/G]GCTGGTCTTGAACTC	55159
rs4888264	snp	G/T	0.447938	0.152711	intron-variant	RFWD3	GRCh38.p7	16:74647734	GTAGCTGGGATTATA[G/T]GCGCCTGCCAACATA	55159
rs4888265	snp	C/T	0.446902	0.154045	intron-variant	RFWD3	GRCh38.p7	16:74649839	CCCCTCTGTTTGTCA[C/T]TGATTTGTCAGGTCA	55159
rs4888266	snp	C/T	0.352504	0.228019	intron-variant	RFWD3	GRCh38.p7	16:74653906	AAGATTTTTTGACCT[C/T]TTAAAAAAAGAAATG	55159
rs4888267	snp	A/G	0.449599	0.150533	intron-variant	RFWD3	GRCh38.p7	16:74654008	AAAATCCACAATTTA[A/G]AAGTGTTCAATTCAG	55159
rs4888268	snp	A/G	0.194902	0.243853	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664489	GGAGCTGTGGCCCAC[A/G]CCTATAATCCCAGCA	55159
rs4888269	snp	G/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664530	CTGAGGCAGGTAGCT[G/T]GAGACCAGGAGTTGG	55159
rs4888270	snp	A/G	0.351635	0.228408	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664678	CCCTTGAACCCGGAG[A/G]GTGGAGGTTACATTG	55159
rs4888271	snp	A/T	0.471863	0.115225	intron-variant	RFWD3	GRCh38.p7	16:74666220	GATAGATAGATAGAT[A/T]GATTGATTAGATACA	55159
rs4888272	snp	A/C	0.333491	0.235646	intron-variant	RFWD3	GRCh38.p7	16:74666342	TAATACAAGTCTTTA[A/C]TCCACAGTTTCCGTG	55159
rs4888273	snp	A/G	0.208779	0.246578	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668764	GTAACTGTGTTGAAG[A/G]ACATTCGTGTACGCT	55159
rs5817920	in-del	-/A	0.375	0.216506	intron-variant	RFWD3	GRCh38.p7	16:74635472	ACTCCATCTCAAAAG[-/A]AAAAAAAAAAATCAA	55159
rs6564152	snp	A/T	0.336017	0.234736	intron-variant	RFWD3	GRCh38.p7	16:74624821	ggcaatacagcaaga[A/T]tccaatctctacaag	55159
rs6564153	snp	A/C	0.336017	0.234736	intron-variant	RFWD3	GRCh38.p7	16:74624825	atacagcaagaatcc[A/C]atctctacaagaaaa	55159
rs6564154	snp	C/T	0.334871	0.235153	intron-variant	RFWD3	GRCh38.p7	16:74651691	GAATACAAAATGCCA[C/T]TACAAAGTGACTAAC	55159
rs6564155	snp	C/G	0.32955	0.237006	intron-variant	RFWD3	GRCh38.p7	16:74660686	AAGACACAATCTGAA[C/G]AACAGCCAATCTCTA	55159
rs7184754	snp	C/T	0.352721	0.227922	intron-variant	RFWD3	GRCh38.p7	16:74633966	atccagcctggaaga[C/T]agaactagatcttct	55159
rs7185722	snp	A/G	0.341685	0.232581	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621950	AAATCACTCACGATC[A/G]TATGAATTTGCTTCC	55159
rs7187928	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74630269	catggctaacatttt[A/T]ttgtattttcagtag	55159
rs7188581	snp	A/T	0.453697	0.14494	intron-variant	RFWD3	GRCh38.p7	16:74639003	tggtatttatgtatc[A/T]aaacatagaaaaggt	55159
rs7188880	snp	A/T	0.494569	0.0518282	synonymous-codon, intron-variant	RFWD3	GRCh38.p7	16:74630912	GCAACAGCTCCAGAC[A/T]GGACGTCCAGCATTA	55159
rs7190555	snp	A/G			synonymous-codon	RFWD3	GRCh38.p7	16:74636508	AGGGTGAGCAGCTCA[A/G]GACCCATGCTTGGGA	55159
rs7190631	snp	A/G	0.332568	0.235971	intron-variant	RFWD3	GRCh38.p7	16:74648711	cgggaggcagaggtt[A/G]ttgtggtgagctgag	55159
rs7191665	snp	G/T	0.448066	0.152544	intron-variant	RFWD3	GRCh38.p7	16:74655050	ccaagttatccagaa[G/T]atctagctaagacaa	55159
rs7191863	snp	C/G	0.0618563	0.164627	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664845	GGTGACTCCCATACT[C/G]GACAGCAGAAATACA	55159
rs7191921	snp	A/C/T			missense	RFWD3	GRCh38.p7	16:74636483	TTGTGCTTGTGCTGG[A/C/T]CCTGGCTGGAGGGTG	55159
rs7193541	snp	C/T	0.471681	0.115575	missense, intron-variant	RFWD3	GRCh38.p7	16:74630845	CGTCATATACCAGAA[C/T]TGAACCATTGGCCAG	55159
rs7193959	snp	A/T	0.351418	0.228505	intron-variant	RFWD3	GRCh38.p7	16:74631071	AGAACACACTCATAC[A/T]CCCAAACTATCTGGA	55159
rs7195499	snp	C/G	0.348574	0.229746	intron-variant	RFWD3	GRCh38.p7	16:74660075	TAACAATAATAAAAA[C/G]AAGAAGAAAGAGAAA	55159
rs7196362	snp	A/G	0.103438	0.202533	intron-variant	RFWD3	GRCh38.p7	16:74640955	aaataaataaaaTTC[A/G]CAAAGGTATGAAAAA	55159
rs7199068	snp	C/G	0.466618	0.124806	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664365	CATTAAGCAACTCAG[C/G]CTTCAGGAAGACAAA	55159
rs7201075	snp	C/T	0.219648	0.248151	intron-variant	RFWD3	GRCh38.p7	16:74640822	cgggtgcctgtagtc[C/T]cagctactcgtaagg	55159
rs7201320	snp	G/T	0.448195	0.152377	intron-variant	RFWD3	GRCh38.p7	16:74660160	ATCCAGGCTCCAATA[G/T]CAGTGCTAACTCCTC	55159
rs7203192	snp	C/T	0.0217236	0.101931	intron-variant	RFWD3	GRCh38.p7	16:74650356	gtagattcagggctt[C/T]tttttttttttggca	55159
rs7203847	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74630272	ggctaacattttttt[G/T]tattttcagtagaga	55159
rs7204804	snp	C/T	0.338069	0.233974	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623523	TCCCTTCAAGGATAC[C/T]TAAGTGACAGGACAA	55159
rs7205838	snp	A/C	0.450357	0.149522	intron-variant	RFWD3	GRCh38.p7	16:74639002	atggtatttatgtat[A/C]taaacatagaaaagg	55159
rs7342706	snp	G/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74666994	GGGTCCCCCGATAGC[G/T]GAAGCAGCGGTGCTC	55159
rs7342732	snp	A/C	0.351635	0.228408	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664818	TCAACTGCTAGAAAC[A/C]CACATAGGGCGGGTG	55159
rs7499887	snp	A/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662481	ATGTCAATAAACAAA[A/T]ACATGAAAAAAATTA	55159
rs8044278	snp	G/T	0.217851	0.247924	intron-variant	RFWD3	GRCh38.p7	16:74634667	gtgctgggattacag[G/T]catgagccactgtgc	55159
rs8047350	snp	A/C	0.403334	0.197456	intron-variant	RFWD3	GRCh38.p7	16:74645346	tctctgctagagata[A/C]ctcatggatataTag	55159
rs8049056	snp	C/G	0.354665	0.227036	intron-variant	RFWD3	GRCh38.p7	16:74640336	ttcttagtagagaca[C/G]ggtttcatcatgttg	55159
rs8050262	snp	C/T	0.478685	0.10101	intron-variant	RFWD3	GRCh38.p7	16:74627261	tgttacaaatgtgtt[C/T]aatacagttgttacc	55159
rs8050624	snp	A/G	0.353371	0.227628	intron-variant	RFWD3	GRCh38.p7	16:74652792	CTCCTGGAATAACAA[A/G]GCATACTCCAGTTTG	55159
rs8052269	snp	A/G	0.140919	0.224948	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622624	GGTCAGAAGTGTTTT[A/G]TAATAAAAACGATAA	55159
rs8052367	snp	A/G	0.453209	0.145623	intron-variant	RFWD3	GRCh38.p7	16:74624969	actccagcctggacc[A/G]agtaagatactgtca	55159
rs8052923	snp	C/T	0.35207	0.228214	intron-variant	RFWD3	GRCh38.p7	16:74646207	tagcaagaccttgtc[C/T]ctgttaaaaatttaa	55159
rs8055784	snp	C/T	0.333722	0.235565	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663523	gaggccagactggtg[C/T]aggctgaataaatgg	55159
rs8056556	snp	C/G	0.0178098	0.0926698	intron-variant	RFWD3	GRCh38.p7	16:74656716	gcctgcttcagcccc[C/G]caaagtgctgggatt	55159
rs8057095	snp	G/T	0.0854556	0.188216	intron-variant	RFWD3	GRCh38.p7	16:74645726	TTATGCAGCCCATGA[G/T]CATAGTCACAAATAt	55159
rs8058133	snp	A/T	0.450734	0.149016	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623587	TTGATGCCCACTCAC[A/T]TCCTAGATGATGAGA	55159
rs8058261	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74646559	ttgggaggccaaggc[A/G]ggcggatcatgaagt	55159
rs8058880	snp	G/T	0.0659589	0.169201	intron-variant	RFWD3	GRCh38.p7	16:74650420	AGTACTTCCTAAGTG[G/T]CATGAGTATTTCTGA	55159
rs8058922	snp	G/T	0.408511	0.193324	missense	RFWD3	GRCh38.p7	16:74661181	TTGATGTTCTCCACA[G/T]TGTCTTCTCCCAAGA	55159
rs8059780	snp	A/C	0.450609	0.149185	intron-variant	RFWD3	GRCh38.p7	16:74641385	ccaggctggtctcca[A/C]ctcctgacctcagat	55159
rs8060923	snp	A/G	0.209388	0.246679	intron-variant	RFWD3	GRCh38.p7	16:74634823	AAAAAAAAAGGGGGG[A/G]AGGGGGGCGCAGGTA	55159
rs8061670	snp	C/T	0.409382	0.192607	intron-variant	RFWD3	GRCh38.p7	16:74656733	aaagtgctgggatta[C/T]aggcatgagccactg	55159
rs8061942	snp	C/T	0.448708	0.151707	intron-variant	RFWD3	GRCh38.p7	16:74657464	ttcactgacatcacc[C/T]AGGttttctttttct	55159
rs8062783	snp	C/T	0.448708	0.151707	intron-variant	RFWD3	GRCh38.p7	16:74657366	cagtttcctgaatta[C/T]gaaaaagttgatcct	55159
rs9746765	snp	C/T	0.336474	0.234568	intron-variant	RFWD3	GRCh38.p7	16:74656305	agtgagaccttgtct[C/T]gccaaaaaaaaaaaa	55159
rs9922003	snp	C/G	0.0228947	0.104514	intron-variant	RFWD3	GRCh38.p7	16:74639282	gcctcaagtgatcca[C/G]ctgcctcagcctccc	55159
rs9922052	snp	A/C	0.0166325	0.0896639	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74666987	CTTCAATGGGTCCCC[A/C]GATAGCTGAAGCAGC	55159
rs9922988	snp	C/T	0.450231	0.149691	intron-variant	RFWD3	GRCh38.p7	16:74635136	atacaaaaaattagc[C/T]gggtgtggtggcggg	55159
rs9923145	snp	A/G	0.450357	0.149522	intron-variant	RFWD3	GRCh38.p7	16:74652268	GAAGCAGGTATAGCA[A/G]ATAAGGGGGGGAGAC	55159
rs9925807	snp	C/G	0.208169	0.246476	intron-variant	RFWD3	GRCh38.p7	16:74645815	tggagtgtagcggca[C/G]aatctcggctcactg	55159
rs9927167	snp	A/C	0.0123036	0.0774623	intron-variant	RFWD3	GRCh38.p7	16:74640774	gaaaccccgtctcta[A/C]taaaaatacaaaaaa	55159
rs9927222	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74632006	TTCAAAGAAACAGGA[A/C]ACATACAGTTTTGTA	55159
rs9929355	snp	A/C	0.00953873	0.0683987	intron-variant	RFWD3	GRCh38.p7	16:74654141	acaagcagtcatttc[A/C]cCTCCTATTTGgtag	55159

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