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
rs15647	snp	A/C	0	0	synonymous-codon	DTL	GRCh38.p7	1:212100943	GTCTGAAATGGTAGG[A/C]AAAGAGAATAGTTCC	51514
rs1017979	snp	C/T	0.0777841	0.181223	intron-variant	DTL	GRCh38.p7	1:212073614	ATATAACTGGAGTTG[C/T]GAAAATGCAACACTA	51514
rs1017980	snp	A/T	0.00755907	0.0610114	intron-variant	DTL	GRCh38.p7	1:212074059	TTGTTAAAAAAAAAA[A/T]TTTTTTTTCCAACAT	51514
rs1062417	snp	A/C	0	0	intron-variant, nc-transcript-variant	DTL, RPL21P28	GRCh38.p7	1:212051497	AAAAAAAAATAAAGG[A/C]CCTCTGGGCTACaaa	51514
rs1316904	snp	A/C	0.152019	0.23	intron-variant	DTL	GRCh38.p7	1:212054409	aaaaccacaCACACA[A/C]AAAAAAAAAAAACAC	51514
rs1316905	snp	A/C	0.0236746	0.106192	intron-variant	DTL	GRCh38.p7	1:212054411	aaCCACACACACAAA[A/C]AAAAAAAAAACACCA	51514
rs1387814	snp	C/G	0.394904	0.203722	utr-variant-3-prime	DTL	GRCh38.p7	1:212103962	CTATCTATACTAAAA[C/G]GCTATTGCTTTTTAT	51514
rs1387815	snp	A/C	0.385359	0.210185	utr-variant-3-prime	DTL	GRCh38.p7	1:212103765	GAATTCAAACCCCAA[A/C]TTGATTTCATAAAAC	51514
rs1387816	snp	G/T	0	0	intron-variant	DTL	GRCh38.p7	1:212069388	ATCTTAGTAGCCTGG[G/T]TATTCCTCATCTATA	51514
rs1574212	snp	A/G	0.137187	0.223099	intron-variant	DTL	GRCh38.p7	1:212055309	ccgtgagcatcaagg[A/G]gtctcccatggctat	51514
rs1578991	snp	C/T	0.417683	0.185425	intron-variant	DTL	GRCh38.p7	1:212037761	cctcggtcatagtgg[C/T]ggtgggctaaatcaa	51514
rs1578992	snp	G/T	0.495291	0.0482933	intron-variant	DTL	GRCh38.p7	1:212037832	cctaccaccacccag[G/T]tcaaaaacaatcaca	51514
rs1578993	snp	G/T	0.493293	0.0575177	intron-variant	DTL	GRCh38.p7	1:212037942	tttttattttacaat[G/T]atttgtattcattca	51514
rs1586660	snp	C/G	0.135484	0.22223	intron-variant	DTL	GRCh38.p7	1:212093189	ccttcttcaatgccc[C/G]ggtgctcagacctct	51514
rs1806360	snp	A/G	0.495095	0.0492773	intron-variant	DTL	GRCh38.p7	1:212097507	tacttgtttggttct[A/G]ttgttaaaactttcc	51514
rs2014029	snp	C/T	0.268995	0.249277	intron-variant	DTL	GRCh38.p7	1:212075594	TCTTTCTTGAAGTAG[C/T]CATACTATACCCTAG	51514
rs2130503	snp	A/G	0.499824	0.00938333	intron-variant	DTL	GRCh38.p7	1:212096179	tcatagtagccttga[A/G]tgatcttttgtattt	51514
rs2130504	snp	G/T	0	0	intron-variant	DTL	GRCh38.p7	1:212074186	CAATTACATGTGTGT[G/T]GTATAGTTTCTTGAT	51514
rs2153037	snp	C/T	0.046775	0.145601	intron-variant	DTL	GRCh38.p7	1:212050468	AGGAGAGGAAATAAA[C/T]TTATAATCAATTTTA	51514
rs2200944	snp	C/G	0.0879971	0.190408	intron-variant	DTL	GRCh38.p7	1:212069647	GCCTCCTGGGTTCAA[C/G]CAATTCTCCTGCCTC	51514
rs2248191	snp	C/T	0.268995	0.249277	intron-variant	DTL	GRCh38.p7	1:212068506	GAATTCTGATGATGA[C/T]TCTTATGAAATGATC	51514
rs2251398	snp	A/G	0.495368	0.0478996	intron-variant	DTL	GRCh38.p7	1:212072450	TATCCTCTGTTTCAA[A/G]AATTATTAGGAAATT	51514
rs2358436	snp	A/C	0.387453	0.208822	intron-variant	DTL	GRCh38.p7	1:212054407	GTAAAACCACACACA[A/C]AAAAAAAAAAAAAAC	51514
rs2358439	snp	G/T	0.135484	0.22223	intron-variant	DTL	GRCh38.p7	1:212074153	TAAGTTTTAATTATA[G/T]GTACATAATTATGTA	51514
rs2358440	snp	A/G	0.499824	0.00938333	intron-variant	DTL	GRCh38.p7	1:212097447	gtctttgttgaattg[A/G]gttaattcaagagcc	51514
rs2884454	snp	A/C	0.0154538	0.0865337	intron-variant	DTL	GRCh38.p7	1:212054410	aaaCCACACACACAA[A/C]AAAAAAAAAAACACC	51514
rs2884455	snp	A/C			intron-variant	DTL	GRCh38.p7	1:212054412	aCCACACACACAAAA[A/C]AAAAAAAAACACCAA	51514
rs2884457	snp	A/G	0.495291	0.0482933	intron-variant	DTL	GRCh38.p7	1:212072838	GCACGATCTTGGCTC[A/G]CTGCAAGCTCCGCCT	51514
rs2884458	snp	A/C			intron-variant	DTL	GRCh38.p7	1:212084931	gctcagattcattat[A/C]tatgatgtagtattt	51514
rs2932543	snp	G/T	0	0	utr-variant-3-prime	DTL	GRCh38.p7	1:212103005	TATTTTTCATCTTGT[G/T]TTAGTGGACCAAAGC	51514
rs2932544	snp	G/T	0	0	synonymous-codon	DTL	GRCh38.p7	1:212102928	AATCTATAATTCTGT[G/T]GAGTGTGCAGGACCA	51514
rs2932545	snp	G/T	0.00330578	0.0405211	missense	DTL	GRCh38.p7	1:212102921	AATTCTGTGGAGTGT[G/T]CAGGACCACACAAGT	51514
rs2932546	snp	C/G			intron-variant	DTL	GRCh38.p7	1:212083293	gctgtcacgagaaca[C/G]catgggaaagacctg	51514
rs2932547	snp	C/G			intron-variant	DTL	GRCh38.p7	1:212083388	tcaggtggggacaca[C/G]ccaaaccatatcaGG	51514
rs2932548	snp	A/G			intron-variant	DTL	GRCh38.p7	1:212083431	ACATAATGGGGCCAA[A/G]GGATAGTGTAAATGT	51514
rs2932549	snp	G/T			intron-variant	DTL	GRCh38.p7	1:212083454	GTAAATGTGGTACTA[G/T]CACTGGATtgaggat	51514
rs2932550	snp	C/G			intron-variant	DTL	GRCh38.p7	1:212083457	AATGTGGTACTATCA[C/G]TGGATtgaggataaa	51514
rs2932551	snp	C/G			intron-variant	DTL	GRCh38.p7	1:212081859	tatcaaacaacatgt[C/G]caaatggaactccag	51514
rs2970588	snp	A/C	0.078151	0.181571	intron-variant, upstream-variant-2KB	INTS7, DTL	GRCh38.p7	1:212033830	ctcatgcctgtaaat[A/C]ccagcactttggaag	51514
rs2970590	snp	A/G	0.0722614	0.17581	intron-variant	DTL	GRCh38.p7	1:212041811	GACCGCGCCCGGCCT[A/G]TTGCATTCTTTTAGT	51514
rs2970591	snp	A/G	0.0777841	0.181223	intron-variant	DTL	GRCh38.p7	1:212046881	ACTGTCTTCCACAAC[A/G]GTTGAATTAATTTAC	51514
rs2970592	snp	A/G	0.499998	0.000998401	intron-variant	DTL	GRCh38.p7	1:212047505	TCTACCCTTTCCCCT[A/G]TCAAAGTTACTGCTT	51514
rs2970593	snp	A/G	0.499897	0.00718776	intron-variant, nc-transcript-variant	DTL, RPL21P28	GRCh38.p7	1:212051873	TTTTGAACAGTACCC[A/G]TTCCCTTGATGTCTA	51514
rs2970594	snp	G/T	0.0722614	0.17581	intron-variant, upstream-variant-2KB	DTL, RPL21P28	GRCh38.p7	1:212052620	ccacactccagcctg[G/T]gcaacagagcgagac	51514
rs2970595	snp	A/T	0.487432	0.0782705	intron-variant, upstream-variant-2KB	DTL, RPL21P28	GRCh38.p7	1:212052740	TACCCATATATATAT[A/T]TTTTTtttcaattac	51514
rs2970596	snp	C/T	0.0718919	0.175435	intron-variant	DTL	GRCh38.p7	1:212057155	gaggctccaagatcc[C/T]cacatggatataatt	51514
rs2970597	snp	A/G	0.0777841	0.181223	intron-variant	DTL	GRCh38.p7	1:212057656	ccataatgataaaaa[A/G]taccagagaaaggaa	51514
rs2970598	snp	C/G	0.0722614	0.17581	intron-variant	DTL	GRCh38.p7	1:212057780	ctttccatttgaaaa[C/G]tacagactgggcaaa	51514
rs2993546	snp	A/T	0.078151	0.181571	intron-variant, upstream-variant-2KB	DTL, RPL21P28	GRCh38.p7	1:212053945	atcttaaattacttg[A/T]cttacaaagagccag	51514
rs2993547	snp	A/G	0.00795532	0.062565	intron-variant, nc-transcript-variant	DTL, RPL21P28	GRCh38.p7	1:212052001	ATTCGCCAAAATGAC[A/G]AACACAAAGGGAAAG	51514
rs2993548	snp	C/G	0.00676609	0.0577691	intron-variant	DTL	GRCh38.p7	1:212043789	aggctagaatgcaat[C/G]gcacgatcttggctc	51514
rs2993549	snp	A/G	0.0777841	0.181223	intron-variant	DTL	GRCh38.p7	1:212042488	GCTGAAATTGTAGGA[A/G]TCTAAAATGTCAATA	51514
rs3010011	snp	C/G	0	0	intron-variant	DTL	GRCh38.p7	1:212093482	cgcggaaagctactt[C/G]tgctcagtggaacct	51514
rs3010012	snp	A/T	0	0	intron-variant	DTL	GRCh38.p7	1:212085206	taactctaaatataG[A/T]TGACTCTCTATATCT	51514
rs3010013	snp	C/G			intron-variant	DTL	GRCh38.p7	1:212081896	gcctccctgacatgt[C/G]catttgggtgtttaa	51514
rs3010014	snp	C/T	0.0777841	0.181223	intron-variant	DTL	GRCh38.p7	1:212055503	ggaatgaggtcgctg[C/T]gtgtggctcccaatt	51514
rs3010015	snp	C/G	0.0722614	0.17581	intron-variant	DTL	GRCh38.p7	1:212055311	gtccgtgagcatcaa[C/G]gggtctcccatggct	51514
rs3010016	snp	C/T	0.135484	0.22223	intron-variant, upstream-variant-2KB	DTL, RPL21P28	GRCh38.p7	1:212053747	aatacaaaaattagc[C/T]gggtgtggtggcatg	51514
rs3010017	snp	C/G	0.0722614	0.17581	intron-variant	DTL	GRCh38.p7	1:212050246	ACTACCTACAAAAAC[C/G]CCCACAAAACACTAA	51514
rs3010018	snp	A/C	0.0777841	0.181223	intron-variant	DTL	GRCh38.p7	1:212050022	CACTGTACCAAGCTA[A/C]TTTTCTGTTTTCTTA	51514
rs3010019	snp	A/G	0.0777841	0.181223	intron-variant	DTL	GRCh38.p7	1:212048628	ATTCAGACACCACTG[A/G]TAAGTTTTTCCCTAG	51514
rs3010020	snp	G/T	0.0777841	0.181223	intron-variant	DTL	GRCh38.p7	1:212048177	AAAAAACAAAAAACA[G/T]GCCATTTAAACCAAA	51514
rs3010021	snp	A/T	0.0517044	0.152246	intron-variant	DTL	GRCh38.p7	1:212047998	GGTTGAACAATGGTA[A/T]TGTAGCTGTTTATAA	51514
rs3010022	snp	C/T	0.0777841	0.181223	intron-variant	DTL	GRCh38.p7	1:212044082	TTAGTTTTTGAGAGA[C/T]AGTCTCGCTATGTCA	51514
rs3010023	snp	C/T	0.5	0	intron-variant	DTL	GRCh38.p7	1:212042477	AGGAATCTAAAATGT[C/T]AATAGCAGCAATTAT	51514
rs3010024	snp	A/C	0.5	0.00019968	intron-variant	DTL	GRCh38.p7	1:212041762	AGCACTTCGGGAGGC[A/C]GAGGCAGGCGGACCA	51514
rs3014308	snp	G/T	0	0	utr-variant-3-prime, downstream-variant-500B	DTL	GRCh38.p7	1:212104944	TGTTCATTAAAATGT[G/T]TATTCCCAAAGTTAT	51514
rs3070845	in-del	-/AAAT			intron-variant	DTL	GRCh38.p7	1:212069215	TTAAAACTAATAAAT[-/AAAT]GATAGTTTTAAAAAG	51514
rs3135474	snp	C/T	0.0717896	0.175331	missense	DTL	GRCh38.p7	1:212100297	CCAAAGCCCCCAGGG[C/T]AAAGTGCAATCCATC	51514
rs3215984	in-del	-/G	0.384401	0.210799	upstream-variant-2KB, intron-variant, utr-variant-5-prime	INTS7, DTL	GRCh38.p7	1:212036025	TGAGTTCAGAATTGG[-/G]AGTCGGCCCTGGTCG	51514
rs3738449	snp	A/G	0.495291	0.0482933	intron-variant	DTL	GRCh38.p7	1:212066721	ATCTAAGTCAGTCTG[A/G]GGAGAAAAGTCGTTT	51514
rs3839029	in-del	-/T	0.111694	0.208258	intron-variant	DTL	GRCh38.p7	1:212080576	TATTTTGAATCTTGA[-/T]TGAAATTTCTTAATT	51514
rs4093391	snp	G/T	0	0	intron-variant	DTL	GRCh38.p7	1:212079993	TATTCTAGATCTTGG[G/T]CCCAAGCCTTTTATG	51514
rs4093392	snp	A/G	0.394904	0.203722	intron-variant	DTL	GRCh38.p7	1:212079927	TGGCCACTGGTACCA[A/G]AGCTGTTCCCCAGCA	51514
rs4093393	snp	G/T	0	0	intron-variant	DTL	GRCh38.p7	1:212079906	TTCCCCAGCATTTGT[G/T]TATATAATTTCTCTA	51514
rs4093394	snp	A/T	0	0	intron-variant	DTL	GRCh38.p7	1:212079878	CTATTTCAGTCACTA[A/T]AGAGAAAGAAAAAAA	51514
rs4309042	snp	A/G	0.0456336	0.143994	intron-variant	DTL	GRCh38.p7	1:212065807	GCCTCCCAGGTTCAC[A/G]CCATTCTCCTGCCTC	51514
rs4394721	snp	C/T	0.384401	0.210799	intron-variant	DTL	GRCh38.p7	1:212056129	aggggctcaagaatt[C/T]gcccacccacctggc	51514
rs4396170	snp	C/T	0.00472811	0.0483911	intron-variant	DTL	GRCh38.p7	1:212056108	accactccacacctc[C/T]tgcccaggggctcaa	51514
rs4397712	snp	A/G	0.0722614	0.17581	intron-variant	DTL	GRCh38.p7	1:212065348	ATTAAGCAGAAAGTG[A/G]TTTTTTTTTTTACAA	51514
rs4951436	snp	G/T	0.114738	0.210248	intron-variant	DTL	GRCh38.p7	1:212062815	GATAGTCTACAAAAT[G/T]TAAACTGAAATATAT	51514
rs4951437	snp	A/G	0.0722614	0.17581	intron-variant	DTL	GRCh38.p7	1:212064321	cactgacaacatcct[A/G]tgcctgagtggtaca	51514
rs4951565	snp	C/T	0.0517044	0.152246	intron-variant	DTL	GRCh38.p7	1:212087945	TTTCTCCTGCCCTAC[C/T]TTTCCCAGCCGGCAC	51514
rs5780672	in-del	-/T			intron-variant	DTL	GRCh38.p7	1:212069169	CTCACCTTTTTTTTT[-/T]CCTCAAAACTTTAAA	51514
rs5780675	in-del	-/T	0.11963	0.213316	intron-variant, downstream-variant-500B	DTL, MIR3122	GRCh38.p7	1:212078026	ATTGGAAATCTGTTG[-/T]TTTTTTTTTCCTAAC	51514
rs5780676	in-del	-/A	0.0788843	0.182262	intron-variant	DTL	GRCh38.p7	1:212090479	GGCTTTGTGACTGAG[-/A]AATAAATAAATACCC	51514
rs6540717	snp	A/T	0.0777841	0.181223	intron-variant	DTL	GRCh38.p7	1:212095700	tgtgtatattaaact[A/T]tccctgcatccctgg	51514
rs6540718	snp	A/C	0.0222566	0.103116	missense	DTL	GRCh38.p7	1:212101071	GACAGAGCGGAAAGA[A/C]ATTGCCAAGCCCGGT	51514
rs6656826	snp	A/G	0.0770498	0.180522	intron-variant	DTL	GRCh38.p7	1:212074343	CAAAGGCCTTTTTAA[A/G]ATTTTGTTTCAGGGA	51514
rs6657728	snp	C/T	0.464523	0.128375	intron-variant	DTL	GRCh38.p7	1:212082353	caaggagttttgtta[C/T]aaaggaaagaagaga	51514
rs6658972	snp	A/G	0.0722614	0.17581	intron-variant, downstream-variant-500B	DTL, MIR3122	GRCh38.p7	1:212077761	TAGGGATCTGAAGAT[A/G]TATATGCTGTGTAAA	51514
rs6670844	snp	A/G	0.418169	0.184985	intron-variant	DTL	GRCh38.p7	1:212061840	gaatgataaataacc[A/G]gaggctggaaagtga	51514
rs6672030	snp	A/G	0.0777841	0.181223	intron-variant	DTL	GRCh38.p7	1:212087068	ACTCCTAGCATAATT[A/G]TTCTAAGGACCTACT	51514
rs6674117	snp	A/G	0.00795532	0.062565	intron-variant	DTL	GRCh38.p7	1:212049344	TATTAACATATTTAA[A/G]TAGTTAGGTATGCTT	51514
rs6675701	snp	A/G	0.135825	0.222405	intron-variant	DTL	GRCh38.p7	1:212088350	GTAATGAAACTTAAC[A/G]AACATTGTTTAATAA	51514
rs6676589	snp	A/G	0.0737376	0.17729	intron-variant	DTL	GRCh38.p7	1:212085419	tgaacatcttttcat[A/G]tgcttattggccatt	51514
rs6683980	snp	C/T	0.0777841	0.181223	intron-variant	DTL	GRCh38.p7	1:212099788	tctggtatgttcctg[C/T]gatagttcttggagc	51514
rs6689563	snp	C/G	0.077417	0.180873	intron-variant	DTL	GRCh38.p7	1:212099451	gttggccaggctagt[C/G]ttgaactcctgacct	51514
rs6690787	snp	A/C	0.145305	0.227022	intron-variant	DTL	GRCh38.p7	1:212081916	gtcagggaggcattt[A/C]gatgtttaattctgc	51514
rs7355066	snp	C/T			intron-variant	DTL	GRCh38.p7	1:212046390	ataccaacccatcac[C/T]taggtattaagccca	51514

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