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
rs15242	snp	A/G	0	0	utr-variant-3-prime	RFWD2	GRCh38.p7	1:175945046	AAATCCAAAACCCAT[A/G]ATGACTTTGGGGAGA	64326
rs471534	snp	A/G	0.406986	0.194565	intron-variant, upstream-variant-2KB	RFWD2	GRCh38.p7	1:176176141	TGATAATGTAAAAAT[A/G]TAAGCAAAAATAAAT	64326
rs484695	snp	A/G	0	0	intron-variant	RFWD2	GRCh38.p7	1:176173308	atttggtttttttga[A/G]acaaagtctcgcact	64326
rs501142	snp	C/T	0.396364	0.202676	intron-variant	RFWD2	GRCh38.p7	1:176187056	TACAGTACCTAAAAA[C/T]TACTATCAAATCAGT	64326
rs513354	snp	C/T	0.396	0.202938	intron-variant	RFWD2	GRCh38.p7	1:176160946	attagcttagttata[C/T]aagaaggaatcaggg	64326
rs520661	snp	A/G	0.39979	0.200158	intron-variant	RFWD2	GRCh38.p7	1:176160140	GTGTTTCTTCAATTC[A/G]AAGCCAAAAAGGAAA	64326
rs539723	snp	C/G	0.0614824	0.164198	upstream-variant-2KB	RFWD2	GRCh38.p7	1:176207523	AAGACGGGAACGTAG[C/G]GGGCGGAAACTCTCG	64326
rs542742	snp	C/T	0.396546	0.202545	intron-variant	RFWD2	GRCh38.p7	1:176171538	ggaaaagttcttgaa[C/T]gaaattaaaagtgct	64326
rs553852	snp	A/T	0.407158	0.194426	intron-variant	RFWD2	GRCh38.p7	1:176149602	AGGCAAAATCAAACA[A/T]CTGAAAACAAAAAAA	64326
rs559341	snp	A/C	0.307423	0.243316	intron-variant	RFWD2	GRCh38.p7	1:176174906	ATTAAAGGTTTCCTA[A/C]AATATCTTAGGGTAG	64326
rs569788	snp	A/T	0.436241	0.166776	upstream-variant-2KB	RFWD2	GRCh38.p7	1:176208462	GTCTCAAAAAAAAAA[A/T]TTTTTTTCATTTGCC	64326
rs580978	snp	A/G	0.407845	0.193868	intron-variant	RFWD2	GRCh38.p7	1:176205997	CCCATCCTTTGAAAT[A/G]GAAGAAGATATTTAC	64326
rs596859	snp	A/G	0.406296	0.19512	intron-variant	RFWD2	GRCh38.p7	1:176198811	caaagatcaaaacag[A/G]catttcacaaaagat	64326
rs598177	snp	C/T	0.306927	0.243432	intron-variant	RFWD2	GRCh38.p7	1:176160774	aaagccaagaaacaa[C/T]agatgctgacgaggc	64326
rs598855	snp	C/T	0.146985	0.227789	intron-variant	RFWD2	GRCh38.p7	1:176172730	TATACTAAAAAATGT[C/T]TTCTAAGTTATTTTC	64326
rs599326	snp	G/T	0.307423	0.243316	intron-variant	RFWD2	GRCh38.p7	1:176172598	GCCTGGTAAAGTAAT[G/T]GAGCATATGTTATAT	64326
rs602933	snp	A/G	0.307423	0.243316	intron-variant	RFWD2	GRCh38.p7	1:176153616	tttattcaacatggt[A/G]atggaagtcttggct	64326
rs611883	snp	A/T	0.406986	0.194565	intron-variant	RFWD2	GRCh38.p7	1:176172061	GACTCTGTCTCAAAA[A/T]TAATTAAATAAAGTT	64326
rs613965	snp	A/G	0.117537	0.212022	intron-variant	RFWD2	GRCh38.p7	1:176153467	ttgctgaacttgttt[A/G]tcagcttaagaagct	64326
rs617078	snp	C/G	0.396364	0.202676	intron-variant	RFWD2	GRCh38.p7	1:176152786	TCTGAACCCAAGTAG[C/G]GGAAACACACATAAA	64326
rs646754	snp	C/T	0.116138	0.211142	intron-variant, upstream-variant-2KB	RFWD2	GRCh38.p7	1:176177485	ATTTAAAATAAACCA[C/T]AAAAGACAATCCCCA	64326
rs659279	snp	A/G	0.396364	0.202676	intron-variant	RFWD2	GRCh38.p7	1:176168419	tccttcctTTCCCCC[A/G]TACTCCCCCCACCCA	64326
rs668154	snp	C/G	0.399968	0.200024	intron-variant	RFWD2	GRCh38.p7	1:176162118	ATGAGATAGGGATTT[C/G]AATGTTGTTGAGAGT	64326
rs670143	snp	A/G	0.413083	0.189483	upstream-variant-2KB	RFWD2	GRCh38.p7	1:176207359	AGACGCTCAGGGCGC[A/G]CCCTCGGGGTCGGGG	64326
rs678516	snp	A/C			intron-variant	RFWD2	GRCh38.p7	1:176173319	ttgtctcaaaaaaac[A/C]aaatgaaaaaaaaaa	64326
rs681027	snp	C/G	0	0	intron-variant	RFWD2	GRCh38.p7	1:176155662	ttcttgggtttcatg[C/G]aacaagaggatctgt	64326
rs704825	snp	A/C	0.307423	0.243316	intron-variant	RFWD2	GRCh38.p7	1:176151973	TTTTTTTTTTTGCAT[A/C]AGACTTTCTAAGCAG	64326
rs704827	snp	A/G	0.405776	0.195535	intron-variant	RFWD2	GRCh38.p7	1:176162550	ATGAGTATCTTTCTT[A/G]CCATATTGTCCCCTC	64326
rs704828	snp	A/G	0.116488	0.211364	intron-variant	RFWD2	GRCh38.p7	1:176163156	GTTTAAGTTATAACT[A/G]TAAGACAGTAGGGAG	64326
rs704829	snp	C/G	0.407158	0.194426	intron-variant	RFWD2	GRCh38.p7	1:176181016	AGGGCACAAGCTGGA[C/G]GCAGCAAATGGGCAA	64326
rs704830	snp	C/T	0.307919	0.243198	intron-variant	RFWD2	GRCh38.p7	1:176192736	TCATATTTTCTTATA[C/T]TGTAATAGAAATTCC	64326
rs791743	snp	C/T	0.400147	0.19989	intron-variant	RFWD2	GRCh38.p7	1:176184306	GCACTAATTACTCAC[C/T]TGTGGGGATAGGTTG	64326
rs791744	snp	A/G	0.407674	0.194008	intron-variant	RFWD2	GRCh38.p7	1:176184522	GATTATGTTACAGTC[A/G]TATTTTTTTTCTTGA	64326
rs791746	snp	A/G	0.395818	0.203069	intron-variant	RFWD2	GRCh38.p7	1:176173798	gtttcaccatgttgg[A/G]taggctggtctcgaa	64326
rs791747	snp	C/T	0.406296	0.19512	intron-variant	RFWD2	GRCh38.p7	1:176196849	GAGCTCAAGACCAGC[C/T]AGGGCAACACAGTGA	64326
rs791748	snp	A/C	0.146985	0.227789	intron-variant	RFWD2	GRCh38.p7	1:176150891	TCTTTTCTTGAAATT[A/C]TTCCTTTAAAAAGAT	64326
rs791749	snp	A/G	0	0	intron-variant	RFWD2	GRCh38.p7	1:176168244	TGGTGAAATCCTGTC[A/G]CTACTAAAGATACAA	64326
rs791750	snp	C/T	0.415727	0.187175	intron-variant	RFWD2	GRCh38.p7	1:176168135	AGGAGGCGGAGGTTG[C/T]GGTGAGCCGAGATCG	64326
rs791751	snp	A/C	0.410399	0.191761	intron-variant	RFWD2	GRCh38.p7	1:176168042	AATTGAATTTTCTTA[A/C]CTCTCTAATGAATAA	64326
rs791752	snp	A/T	0.397633	0.201754	intron-variant	RFWD2	GRCh38.p7	1:176166991	CTTCTTTTATTTTCC[A/T]TAGGTAACCATTGTT	64326
rs791753	snp	G/T	0.407158	0.194426	intron-variant	RFWD2	GRCh38.p7	1:176166018	GGTATATAAGATTTT[G/T]TGGTAAAATTCAATG	64326
rs791793	snp	A/C			intron-variant	RFWD2	GRCh38.p7	1:176160146	CTTCAATTCGAAGCC[A/C]AAAAGGAAACCAAGA	64326
rs791794	snp	A/C			intron-variant	RFWD2	GRCh38.p7	1:176160157	AGCCCAAAAGGAAAC[A/C]AAGACTAATGCTGGC	64326
rs791800	snp	C/T	0.408188	0.193589	intron-variant	RFWD2	GRCh38.p7	1:176202664	ATAGGGAGAGCCCTG[C/T]CTCAAAAAAAGGAAA	64326
rs791801	snp	G/T	0.408017	0.193729	intron-variant	RFWD2	GRCh38.p7	1:176190921	CAAAGGTTAAATACT[G/T]AAAAATAATAATATT	64326
rs796933	snp	C/G	0.307423	0.243316	intron-variant	RFWD2	GRCh38.p7	1:176149581	GATTTTGCCTGAAAT[C/G]TTCCATAGAAATATA	64326
rs796934	snp	C/T	0.308908	0.242961	intron-variant	RFWD2	GRCh38.p7	1:176168251	GCCAACATGGTGAAA[C/T]CCTGTCACTACTAAA	64326
rs812066	snp	C/T	0.0364509	0.129988	intron-variant	RFWD2	GRCh38.p7	1:176196655	aaactatggcttcac[C/T]agtaagttccaccaa	64326
rs813180	snp	A/G	0.399432	0.200425	intron-variant	RFWD2	GRCh38.p7	1:176197006	GTTACGGGTTAAATT[A/G]TATTTCCATCCCTCG	64326
rs813776	snp	C/G			intron-variant	RFWD2	GRCh38.p7	1:176173210	cagctactagggagg[C/G]tgaggcaggagaatc	64326
rs944365	snp	C/T	0.396364	0.202676	intron-variant	RFWD2	GRCh38.p7	1:176121442	ATCTGTCAACAACAA[C/T]AACAGCAGCAGCTAA	64326
rs998631	snp	A/G	0.116138	0.211142	intron-variant	RFWD2	GRCh38.p7	1:176071912	TTTTCCCTTGCCTTT[A/G]TTAGAGGCTTGTCAG	64326
rs1053035	snp	A/C	0	0	utr-variant-3-prime	RFWD2	GRCh38.p7	1:175944952	CCCAGCCAACTCTCC[A/C]CCATCAATGTAACTC	64326
rs1053045	snp	C/T	0	0	utr-variant-3-prime	RFWD2	GRCh38.p7	1:175944879	ATAGGGAAACAAATT[C/T]TTTTGAATAAAAATA	64326
rs1143376	snp	A/G			intron-variant, downstream-variant-500B, utr-variant-3-prime	RFWD2, SCARNA3	GRCh38.p7	1:175968050	tgaaatcctgtctct[A/G]ctgaaaacacaaaaa	64326
rs1155229	snp	A/G	0.44768	0.153045	intron-variant	RFWD2	GRCh38.p7	1:175959152	ttaacctaatattaa[A/G]ccaactttacattcg	64326
rs1330863	snp	C/T	0.084728	0.187577	intron-variant	RFWD2	GRCh38.p7	1:176133672	AAATGCACCGTACTG[C/T]CACAATTTCATAAAA	64326
rs1357337	snp	A/G	0.406123	0.195258	intron-variant	RFWD2	GRCh38.p7	1:175961801	TTTGTGACCTAATCT[A/G]TGAAGCCTTTCTTAT	64326
rs1357338	snp	C/T	0.1652	0.235179	intron-variant	RFWD2	GRCh38.p7	1:175961750	CTCTCTTCTTACTTC[C/T]TCAGTTGCCCCTTTG	64326
rs1509753	snp	C/T	0.0310518	0.120672	intron-variant	RFWD2	GRCh38.p7	1:176178328	gcaacatggcaaaac[C/T]ctgtctctacaaaaa	64326
rs1522637	snp	C/T	0.309401	0.24284	intron-variant	RFWD2	GRCh38.p7	1:175954461	attaacttttcattt[C/T]aatacttttttacct	64326
rs1704032	snp	C/T	0	0	intron-variant	RFWD2	GRCh38.p7	1:176190964	AGAGCCAGGCACAAT[C/T]TAGAGTCATTTAGAA	64326
rs1770643	snp	C/T	0.407158	0.194426	intron-variant	RFWD2	GRCh38.p7	1:176158833	ggcaacatggtaaaa[C/T]cctgtctctactaaa	64326
rs1831447	snp	C/G	0.309894	0.242719	intron-variant	RFWD2	GRCh38.p7	1:176106611	tatgcccccacccag[C/G]aattgacccagtgca	64326
rs1974142	snp	C/G	0.396182	0.202807	intron-variant	RFWD2	GRCh38.p7	1:176106566	gatcagctggcaaca[C/G]ccagattgattaact	64326
rs2039230	snp	C/T	0.409721	0.192325	intron-variant	RFWD2	GRCh38.p7	1:176205655	TACCAATATCTAAAA[C/T]CCAATAAAAATTCCA	64326
rs2039231	snp	A/G	0.445064	0.156365	intron-variant	RFWD2	GRCh38.p7	1:176109268	TCTTTCTTCATTTCT[A/G]TAGTTCTATTGCTGT	64326
rs2039232	snp	C/T	0.307671	0.243257	intron-variant	RFWD2	GRCh38.p7	1:176142391	atattaaataaatgg[C/T]ctaaatacacaatta	64326
rs2039233	snp	G/T	0.0174175	0.0916809	intron-variant	RFWD2	GRCh38.p7	1:176090938	AAAGAAACCCACAGT[G/T]AGACACACTAAGGTG	64326
rs2457418	snp	A/C	0.395087	0.203592	intron-variant	RFWD2	GRCh38.p7	1:176196033	GAAACATGGATTATT[A/C]AGAAGTATGTTGTTT	64326
rs2481626	snp	A/T	0.116138	0.211142	intron-variant	RFWD2	GRCh38.p7	1:176124869	ctggtgggaatgtaa[A/T]ttagtacaaccacta	64326
rs2481627	snp	A/C	0.40595	0.195396	intron-variant	RFWD2	GRCh38.p7	1:176123031	CAAACTAGTCAAATA[A/C]ACCACGTTGTGTAAT	64326
rs2481628	snp	A/G	0.396727	0.202413	intron-variant	RFWD2	GRCh38.p7	1:176117505	TGTTGATAGTTTTTT[A/G]TGTAAGGCTTATTTA	64326
rs2481629	snp	C/G	0.149999	0.229128	intron-variant	RFWD2	GRCh38.p7	1:176116276	CTCCTACCTCAGCCT[C/G]TCAAGTAGCTGGCCC	64326
rs2481630	snp	A/G	0.407502	0.194147	intron-variant	RFWD2	GRCh38.p7	1:176114275	TGTAGATTGGTTTGT[A/G]TCTGTTTCTGAACGG	64326
rs2481631	snp	A/G	0.410568	0.191619	intron-variant	RFWD2	GRCh38.p7	1:176114178	GCCTTAAATTGAAAT[A/G]TACCGTAGGAACTTg	64326
rs2481632	snp	A/G	0.116488	0.211364	intron-variant	RFWD2	GRCh38.p7	1:176113546	ATTAACACTACTTTG[A/G]AATTTCTAGCAAATC	64326
rs2481633	snp	A/G	0.396	0.202938	intron-variant	RFWD2	GRCh38.p7	1:176113080	ctgtcatatgttcca[A/G]caaccccactgctgg	64326
rs2481634	snp	C/G	0.40733	0.194287	intron-variant	RFWD2	GRCh38.p7	1:176113064	caaccccactgctgg[C/G]tatatatccaaaaga	64326
rs2481635	snp	A/C	0.288646	0.246995	intron-variant	RFWD2	GRCh38.p7	1:176111301	TCTCACACACACACA[A/C]AAAATAAATAAAAAT	64326
rs2481636	snp	C/T	0.146985	0.227789	intron-variant	RFWD2	GRCh38.p7	1:176108912	GTTGGACAGGATGGT[C/T]TCGATCTCTTGACCT	64326
rs2481637	snp	A/G	0.116138	0.211142	intron-variant	RFWD2	GRCh38.p7	1:176099779	ggaaccctctacagc[A/G]gctgtgtagacaagg	64326
rs2481638	snp	C/T	0.0364509	0.129988	intron-variant	RFWD2	GRCh38.p7	1:176097933	tttccttttaaaaaa[C/T]atttgatcaaagtgt	64326
rs2481639	snp	C/T	0.307423	0.243316	intron-variant	RFWD2	GRCh38.p7	1:176095473	aggctggtctggatc[C/T]ggactcaagcaatct	64326
rs2481640	snp	A/G	0.150667	0.229419	intron-variant	RFWD2	GRCh38.p7	1:176091693	GTTCGATTGTTACCT[A/G]TTCTATCACTGTGCT	64326
rs2481641	snp	G/T	0.444666	0.15686	intron-variant	RFWD2	GRCh38.p7	1:176089646	AGTGAAGCAGTGCTT[G/T]AAAATATGACTCTTA	64326
rs2481642	snp	C/T	0.446771	0.154211	intron-variant	RFWD2	GRCh38.p7	1:176089167	TAGCTGGGGTCCTGC[C/T]ACTGTGCCCGGCTGA	64326
rs2481643	snp	A/T	0.0360663	0.129354	intron-variant	RFWD2	GRCh38.p7	1:176088990	tttttttttggagac[A/T]gagttttgctcttgt	64326
rs2481644	snp	A/G	0.116488	0.211364	intron-variant	RFWD2	GRCh38.p7	1:176084406	GTGGCCATTTTCACA[A/G]TATTGATTCTTCCTA	64326
rs2481645	snp	C/G	0.0622301	0.165053	intron-variant	RFWD2	GRCh38.p7	1:176083896	ATGGCTGTATTGTAC[C/G]TAAAACATGTCTCTA	64326
rs2481646	snp	C/T	0.391769	0.205917	intron-variant	RFWD2	GRCh38.p7	1:176083461	TGTAACCTCATAAGT[C/T]AAAATCAATTACTAT	64326
rs2481647	snp	A/T	0.406468	0.194981	intron-variant	RFWD2	GRCh38.p7	1:176081540	ATTATTGTTATTATT[A/T]TTTTTCCAAGGAATT	64326
rs2481648	snp	C/T	0.116838	0.211584	intron-variant	RFWD2	GRCh38.p7	1:176080446	ataggctgtattttt[C/T]tgttttctgttatca	64326
rs2481649	snp	A/G	0.116138	0.211142	intron-variant	RFWD2	GRCh38.p7	1:176078766	tttcttgtagatttt[A/G]gagattaggcctttg	64326
rs2481650	snp	A/G	0.116138	0.211142	intron-variant	RFWD2	GRCh38.p7	1:176078384	ctttccccattgctt[A/G]tttttgttgattttg	64326
rs2481651	snp	A/G	0.406123	0.195258	intron-variant	RFWD2	GRCh38.p7	1:176078273	acctaccagtgccat[A/G]ctgttttggttattg	64326
rs2481652	snp	A/G	0.149665	0.228982	intron-variant	RFWD2	GRCh38.p7	1:176078095	ggtattttaaggata[A/G]cattggatctgtaaa	64326
rs2481653	snp	G/T	0.307919	0.243198	intron-variant	RFWD2	GRCh38.p7	1:176074985	TACTTTGGAGCAACA[G/T]ATTAGCATTCTTACT	64326
rs2481654	snp	C/T	0.0626037	0.165477	intron-variant	RFWD2	GRCh38.p7	1:176074584	GTTTGGAAATACTTA[C/T]AAATTGTGGTTAGAT	64326
rs2481655	snp	G/T	0.391769	0.205917	intron-variant	RFWD2	GRCh38.p7	1:176072685	CTTTTAATATGTTCC[G/T]TATTGTAGAGTGCTT	64326

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