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
rs887	snp	C/T	0.367913	0.220446	utr-variant-3-prime, intron-variant, downstream-variant-500B	EML6, RTN4	GRCh38.p7	2:54971932	CACCAATGTTTTAAC[C/T]CACATATATCATACA	400954
rs1022	snp	C/T	0	0	utr-variant-3-prime, intron-variant, downstream-variant-500B	EML6, RTN4	GRCh38.p7	2:54971937	TCATGCACCAATGTT[C/T]TAACTCACATATATC	400954
rs15028	snp	A/C	0.084364	0.187256	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	EML6, RTN4	GRCh38.p7	2:54972374	TTAGATTCAGTCCAT[A/C]GATTCTGTGACAAAA	400954
rs15029	snp	A/T	0.149999	0.229128	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	EML6, RTN4	GRCh38.p7	2:54972306	TTTTGTAATTAATAA[A/T]TTCTTGCATAACAAT	400954
rs149381	snp	A/G	0.00318978	0.0398085	intron-variant	EML6	GRCh38.p7	2:54784610	ttaactactaatagc[A/G]tgctgttgacaagaa	400954
rs164854	snp	A/G	0.178785	0.239642	intron-variant	EML6	GRCh38.p7	2:54765145	TTCTAAAACTTCTAC[A/G]ATCACTTAAATTTAA	400954
rs164855	snp	A/G	0.234692	0.249531	intron-variant	EML6	GRCh38.p7	2:54792514	GTAAATGTTGATAGC[A/G]GCTATATTTGTGATT	400954
rs164941	snp	A/G	0.0626037	0.165477	intron-variant	EML6	GRCh38.p7	2:54766455	tatataaacaaaatt[A/G]taagaaaacactgga	400954
rs164942	snp	C/G	0.195197	0.246425	intron-variant	EML6	GRCh38.p7	2:54789147	TTTTTGTTTGTTTAC[C/G]CAAGTATCTTCCAGA	400954
rs164943	snp	G/T	0.499693	0.0123764	intron-variant	EML6	GRCh38.p7	2:54792732	TTGAAGTATTTTTTA[G/T]ACCTAATACTATGGG	400954
rs165048	snp	C/T	0.41833	0.184838	intron-variant	EML6	GRCh38.p7	2:54790062	AGGGAGATCTAAGAA[C/T]AGTCAGCATTAAGTA	400954
rs165049	snp	C/T	0.106633	0.204807	intron-variant	EML6	GRCh38.p7	2:54790159	GTAATGACTAGTGAT[C/T]TTTATAAGAGAGATT	400954
rs165050	snp	C/G	0.411914	0.190483	intron-variant	EML6	GRCh38.p7	2:54790918	TTTTAGTAGAGACGG[C/G]GTTTCACCATGTTAG	400954
rs165051	snp	C/G	0.389903	0.207189	intron-variant	EML6	GRCh38.p7	2:54792586	ACTGTTGCGTATCTG[C/G]ATTACTGTGGTGGTT	400954
rs165052	snp	G/T	0.497211	0.037236	intron-variant	EML6	GRCh38.p7	2:54794621	TAGGAAAACTTATCT[G/T]ACCAATGGCCCTTGC	400954
rs165053	snp	A/G	0.48498	0.0853497	intron-variant	EML6	GRCh38.p7	2:54794754	TTAAACAAGTGTTCA[A/G]CTTACAAAAATTGTA	400954
rs165054	snp	C/T	0.241914	0.249869	intron-variant	EML6	GRCh38.p7	2:54794784	ACGACATTACGCTTA[C/T]GTGACAAGTGTAATA	400954
rs168507	snp	C/T	0.489259	0.0724914	intron-variant	EML6	GRCh38.p7	2:54737077	tcccacattcaaatt[C/T]caccaattgtcccaa	400954
rs168508	snp	C/G	0.436123	0.166908	intron-variant	EML6	GRCh38.p7	2:54735787	CTCTTATAAACACTT[C/G]AACAGATTTTCAAAA	400954
rs168530	snp	C/T	0	0	intron-variant	EML6	GRCh38.p7	2:54760850	TCCCAGATTCTTTTT[C/T]TAGTaaaaaaaaaaa	400954
rs171349	snp	A/G	0.413416	0.189196	intron-variant	EML6	GRCh38.p7	2:54789024	AAGAATAAAAAGCAA[A/G]AAGATAGCAAACCTG	400954
rs173304	snp	C/G	0.151334	0.229706	intron-variant	EML6	GRCh38.p7	2:54741079	GCTGTGATCGTGTGG[C/G]CTGCACTGTCATTTA	400954
rs181348	snp	C/T	0.474634	0.109726	intron-variant	EML6	GRCh38.p7	2:54730068	GCTTACTGCAACCTC[C/T]GCCTCCTGGGCCAAA	400954
rs187122	snp	A/T	0.0426619	0.140095	intron-variant	EML6, LOC105374667	GRCh38.p7	2:54750005	CATCAAGGAAAAAAA[A/T]TGATCTGGACCTAGT	400954
rs187140	snp	A/G			intron-variant	EML6	GRCh38.p7	2:54797367	atggtctggccttga[A/G]acctctctcaaacct	400954
rs189569	snp	A/C	0	0	intron-variant	EML6	GRCh38.p7	2:54789435	aggaaaatggcgtga[A/C]cccgggaggccggag	400954
rs241662	snp	A/G	0.358728	0.225118	intron-variant	EML6	GRCh38.p7	2:54725899	TTGTGTGGGCTGGCT[A/G]GTAGGATTTTGTGAT	400954
rs241868	snp	C/T	0	0	intron-variant	EML6	GRCh38.p7	2:54760856	AGTCTGTCCCAGATT[C/T]TTTTTTTAGTaaaaa	400954
rs354194	snp	C/T	0.127944	0.218179	intron-variant	EML6	GRCh38.p7	2:54769619	ACTCATCAAGTTGTA[C/T]ACTTTAAATACATAC	400954
rs354195	snp	C/T	0.436692	0.166271	intron-variant	EML6	GRCh38.p7	2:54738187	aggcagagcagtgaa[C/T]gaaacagccctgccc	400954
rs354196	snp	C/T	0.41141	0.19091	intron-variant	EML6	GRCh38.p7	2:54739270	atctcaaacatcagg[C/T]atattcatccctact	400954
rs354197	snp	C/T	0.432357	0.171014	intron-variant	EML6	GRCh38.p7	2:54740185	CTCCTACACATACAC[C/T]GAAACTCTCACAGCT	400954
rs354198	snp	C/T	0.499368	0.0177603	intron-variant	EML6	GRCh38.p7	2:54740833	AACCCCTCACATACA[C/T]AAACAGGGCCAGTCA	400954
rs354199	snp	A/G	0.484066	0.0878235	intron-variant	EML6	GRCh38.p7	2:54741258	catcaaagccaggag[A/G]ccagttagtactcta	400954
rs354200	snp	A/G	0.485528	0.0838238	intron-variant	EML6	GRCh38.p7	2:54743106	ctgaactgaataaac[A/G]agtaaatcattatct	400954
rs354201	snp	A/G	0.485118	0.0849685	intron-variant	EML6	GRCh38.p7	2:54743217	tgagtgcaactgtgt[A/G]tgtgcgtgcaccctg	400954
rs354202	snp	C/T	0.077417	0.180873	intron-variant	EML6	GRCh38.p7	2:54743806	ATTTAATGTAAATGT[C/T]ATATGTGTTTTATAA	400954
rs354203	snp	C/G	0.0138799	0.0821421	intron-variant	EML6	GRCh38.p7	2:54743925	CACTAGTCAAATTTA[C/G]CTTCCTTCCTCTATT	400954
rs354204	snp	C/T	0.282105	0.24793	intron-variant	EML6	GRCh38.p7	2:54744248	CATTATGGGTCCTTC[C/T]TTTCCCCACAAAAGA	400954
rs354205	snp	C/T	0.193028	0.243422	intron-variant, downstream-variant-500B	EML6, LOC105374667	GRCh38.p7	2:54745339	GAAGGCACTATCCCA[C/T]CTGGATCTCCATCCA	400954
rs354206	snp	A/G	0.195837	0.244062	intron-variant, downstream-variant-500B	EML6, LOC105374667	GRCh38.p7	2:54745713	gttcactgcagccac[A/G]atttcctgggctcaa	400954
rs354235	snp	A/C	0.496279	0.0429702	intron-variant	EML6	GRCh38.p7	2:54737157	acattctcttatata[A/C]ctgcattgctacaat	400954
rs354236	snp	A/C	0.436265	0.166749	intron-variant	EML6	GRCh38.p7	2:54735692	AGTCAAAATACCTTA[A/C]GCACAAACATTCAAA	400954
rs354237	snp	G/T	0.437824	0.164991	intron-variant	EML6	GRCh38.p7	2:54732759	ATATAAAAATCTATA[G/T]GTCACTCATTAGCTC	400954
rs354238	snp	C/T	0.439641	0.162899	intron-variant	EML6	GRCh38.p7	2:54732653	GATTATTTCCATTTC[C/T]GGATCCCCAAACATT	400954
rs354239	snp	C/T	0.36021	0.224397	intron-variant	EML6	GRCh38.p7	2:54727687	AGAATTAGAAACGAA[C/T]AAGTTTTGATATTCA	400954
rs354240	snp	C/T	0.00438332	0.0466095	intron-variant	EML6	GRCh38.p7	2:54726922	TAGTTCAGTGAACTG[C/T]CACATTAATATTATT	400954
rs354241	snp	G/T	0.361684	0.223667	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	EML6	GRCh38.p7	2:54724751	cgGGCTCCGGCCCCC[G/T]GGAGAGGCTCTCGGG	400954
rs354242	snp	C/G	0.362313	0.223351	upstream-variant-2KB, intron-variant	EML6	GRCh38.p7	2:54724316	TGTTTCCCTAATAAG[C/G]GAGGGCGAATATGCA	400954
rs354944	snp	A/G	0.364609	0.222182	intron-variant	EML6	GRCh38.p7	2:54795816	TGAAAACGCTGATGA[A/G]TGCAGAGGCATAGAT	400954
rs354945	snp	C/G	0.243347	0.249911	intron-variant	EML6	GRCh38.p7	2:54796069	TTTAAAACTTTCTCA[C/G]AGAAAAATTATAACA	400954
rs354946	snp	C/G	0.256149	0.255089	intron-variant	EML6	GRCh38.p7	2:54796886	CAGGTAGTCACAAGG[C/G]GGGGATCCTTTAAAA	400954
rs354947	snp	A/G	0.228842	0.249103	intron-variant	EML6	GRCh38.p7	2:54797546	ggtttcctagtgcat[A/G]taaagtcatgtttat	400954
rs354948	snp	G/T	0.228547	0.249078	intron-variant	EML6	GRCh38.p7	2:54797672	cttcagcTAAGGTCT[G/T]TGGGAAGTGGTTGGT	400954
rs354949	snp	C/T	0.227369	0.248974	intron-variant	EML6	GRCh38.p7	2:54797822	gcaagttacttgact[C/T]ctctgggcttcagtg	400954
rs354950	snp	G/T	0.186737	0.241863	intron-variant	EML6	GRCh38.p7	2:54798146	tcttcttgtctttaa[G/T]ttttctatgtagtat	400954
rs723975	snp	A/G	0.250168	0.25	intron-variant	EML6	GRCh38.p7	2:54865789	TCCAATGCTTTCACC[A/G]ATATTTGATTTACAT	400954
rs733916	snp	A/G	0.221444	0.248364	synonymous-codon	EML6	GRCh38.p7	2:54928414	CATCAGGGCTGTGTC[A/G]GCGCCGCCCACCGTG	400954
rs755229	snp	A/G	0.498871	0.0237351	intron-variant	EML6	GRCh38.p7	2:54929159	GAGTTGTGAAAAACC[A/G]TCTTCCATTCTAACC	400954
rs755230	snp	A/T	0.499663	0.0129749	intron-variant	EML6	GRCh38.p7	2:54929262	CAGGTGGGTTTGGCA[A/T]TTCCAGCCTATCCCA	400954
rs868699	snp	C/T	0.039522	0.134904	intron-variant	EML6	GRCh38.p7	2:54759043	ACAAGAATACTGGGT[C/T]GTGTGCTGAGTGCCA	400954
rs868700	snp	A/T	0.454664	0.143571	intron-variant	EML6	GRCh38.p7	2:54759014	CAAGCACTCCATCCC[A/T]ATTTTTTGTTTTCAA	400954
rs881427	snp	C/T	0.334642	0.235236	intron-variant	EML6	GRCh38.p7	2:54948145	AGAGGAGTACGCCAG[C/T]TCTTGGTGACGTGGG	400954
rs891745	snp	A/G	0.499732	0.0115784	intron-variant	EML6	GRCh38.p7	2:54852554	AATTCCACCAGTACA[A/G]GGGCATTTGGAATTC	400954
rs891777	snp	C/T	0.248188	0.249993	intron-variant	EML6	GRCh38.p7	2:54897986	CCGTGCCACCAAAAC[C/T]GGCAAAGTGGATCTA	400954
rs891778	snp	A/G	0.256061	0.249927	intron-variant	EML6	GRCh38.p7	2:54897275	GAAGTGAAAAGCCTT[A/G]GTCAAGCATAAAACA	400954
rs919669	snp	C/T	0.289424	0.246872	intron-variant	EML6	GRCh38.p7	2:54890277	TAGAGACAAACATCA[C/T]AAATATTAGCAAACA	400954
rs930184	snp	C/T	0.00279162	0.0372561	intron-variant	EML6	GRCh38.p7	2:54831163	ACTCTGCTCTCTAAG[C/T]ACATGTTTTGGTTTC	400954
rs930185	snp	A/G	0.243919	0.249926	intron-variant	EML6	GRCh38.p7	2:54830824	GGATTAGTTGACTTA[A/G]ATGCACATTTTTGTA	400954
rs930493	snp	A/G	0.495445	0.0475058	intron-variant	EML6	GRCh38.p7	2:54831061	AGCTTGCAAGTACCC[A/G]TAAGAGCAATTTTTT	400954
rs974916	snp	C/T	0.462144	0.132269	intron-variant	EML6	GRCh38.p7	2:54776107	CAGCCTCACAGGGgt[C/T]caacctgccttattt	400954
rs980644	snp	C/T	0.45692	0.1403	intron-variant	EML6	GRCh38.p7	2:54757287	tatttaagagcaaga[C/T]ccctgaaagcaaatt	400954
rs993362	snp	A/G	0.25801	0.249872	intron-variant	EML6	GRCh38.p7	2:54826037	ATTCAGACTGTGCCC[A/G]GGTGGCAGGAAATTC	400954
rs993541	snp	A/T	0.477515	0.103619	intron-variant	EML6	GRCh38.p7	2:54851060	atcctgaatgaggta[A/T]cattcccatgcattg	400954
rs997198	snp	A/T	0.401924	0.198543	intron-variant	EML6	GRCh38.p7	2:54894714	ATGCTGAGAACGTGC[A/T]TAATCTTGCTTAGGG	400954
rs998230	snp	C/G	0.495521	0.0471118	intron-variant	EML6	GRCh38.p7	2:54894793	ACCAGAGTTTTCCAT[C/G]TCATATATTTAGGAA	400954
rs1006632	snp	G/T	0	0	intron-variant	EML6	GRCh38.p7	2:54898382	GCTCAGTCTATAGAA[G/T]AGCTTCAAGCAGAGT	400954
rs1159853	snp	G/T	0.0482946	0.147699	intron-variant	EML6	GRCh38.p7	2:54741754	gacatctgggataat[G/T]tgagcatgaattata	400954
rs1238352	snp	A/C	0	0	intron-variant	EML6	GRCh38.p7	2:54806698	tgttattaATTAACC[A/C]CCATGTGATAGACCC	400954
rs1347816	snp	C/T	0.39979	0.200158	intron-variant	EML6	GRCh38.p7	2:54851057	ctgaatgaggtatca[C/T]tcccatgcattgtta	400954
rs1347817	snp	C/T	0.463774	0.129618	intron-variant	EML6	GRCh38.p7	2:54802490	ATAGGCACATGCCAC[C/T]ATGTCTGGCTAATTT	400954
rs1371019	snp	C/T	0.126564	0.217402	intron-variant	EML6	GRCh38.p7	2:54865730	TTGAGTATTCCTTAT[C/T]TGAAATGTTTGGGAT	400954
rs1371020	snp	A/G	0.306927	0.243432	intron-variant	EML6	GRCh38.p7	2:54860750	gaagccgctgcaagt[A/G]cctacaagtccatat	400954
rs1371021	snp	A/G	0.453818	0.144769	intron-variant	EML6	GRCh38.p7	2:54855393	AGCATCATCCTCTTG[A/G]TGCTGTCCTAAAAGT	400954
rs1432104	snp	A/G	0.437965	0.164831	intron-variant	EML6	GRCh38.p7	2:54888862	GATATTTGCCTAAAT[A/G]AGCTGAAAACTTATG	400954
rs1438814	snp	A/T	0.364609	0.222182	intron-variant	EML6	GRCh38.p7	2:54840602	AAGAACATTCAAAGA[A/T]GGGATATATTCATTC	400954
rs1438815	snp	C/T	0.347473	0.230215	intron-variant	EML6	GRCh38.p7	2:54840579	ATTCATTCCTTTATT[C/T]CAGAAATTTTTATTC	400954
rs1438816	snp	A/G	0.321053	0.23969	intron-variant	EML6	GRCh38.p7	2:54781942	GTGGCTCACACCTGT[A/G]ATCCCAGCACTTTGG	400954
rs1438817	snp	A/G	0.204189	0.245767	intron-variant	EML6	GRCh38.p7	2:54893814	GCCAGCAAAACAACC[A/G]TTACAGTTGCATACC	400954
rs1438818	snp	C/T	0.492435	0.0610346	intron-variant	EML6	GRCh38.p7	2:54893522	GCCTCTGTAACAGTA[C/T]TAAGATGTGGGAACT	400954
rs1465672	snp	C/G	0.234982	0.249549	intron-variant	EML6	GRCh38.p7	2:54840075	AGCATTATCAGGAAG[C/G]AAAGAGTTAATGATT	400954
rs1465673	snp	A/C	0.478271	0.101943	intron-variant	EML6	GRCh38.p7	2:54839917	AAATATCGACATTAA[A/C]TATATATCTATATAT	400954
rs1510613	snp	A/G	0.492727	0.0598633	intron-variant	EML6	GRCh38.p7	2:54744493	GGATTTTAGACATAC[A/G]GACTTATAAAAAAGT	400954
rs1510614	snp	C/T	0.475348	0.108251	intron-variant	EML6, LOC105374667	GRCh38.p7	2:54747760	ATTGATTTCATCCCA[C/T]GTTATTTATCCTTAA	400954
rs1541892	snp	A/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	EML6	GRCh38.p7	2:54827974	CTACTGTGGATGACA[A/T]AAATCAAGCAATTAA	400954
rs1549839	snp	G/T	0.110167	0.207236	intron-variant	EML6	GRCh38.p7	2:54837356	gaggaaataacagca[G/T]agaaagtttgtatta	400954
rs1549840	snp	A/G	0.45692	0.1403	intron-variant	EML6	GRCh38.p7	2:54835976	GCCGCCCGCGGGACT[A/G]GAGAATAGGATGTGC	400954
rs1560567	snp	C/G	0	0	intron-variant	EML6	GRCh38.p7	2:54900228	ATGCACTAGAACTAT[C/G]AGGTGTACTGAGAGG	400954
rs1614026	snp	A/G	0.178144	0.239451	intron-variant	EML6	GRCh38.p7	2:54765620	ACAGAAAACTTAGCC[A/G]GACATAGGGCGGGTG	400954
rs1624761	snp	C/T			intron-variant	EML6	GRCh38.p7	2:54789401	cgcctgtagtcccag[C/T]tactcgggaggctga	400954

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