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
rs724909	snp	A/C	0.483995	0.0880135	intron-variant	SCAF11	GRCh38.p7	12:45929928	AGTAAAAACTGTTTC[A/C]ATTTTTGACTGTGTT	9169
rs735351	snp	A/T	0.417683	0.185425	intron-variant	SCAF11	GRCh38.p7	12:45935409	AGGCTGAGTTCCGGA[A/T]CTTACTGCCTTACCC	9169
rs764192	snp	A/C	0.193966	0.243639	intron-variant	SCAF11	GRCh38.p7	12:45969244	ACTTCTGATTCCCCG[A/C]GGCTTGAGGTACCCA	9169
rs997307	snp	A/G	0.474634	0.109726	intron-variant	SCAF11	GRCh38.p7	12:45953341	TATGAAATTTCTTAA[A/G]AGATTATATTAATGC	9169
rs997308	snp	C/T	0.0228947	0.104514	intron-variant	SCAF11	GRCh38.p7	12:45953538	AACAGAGTGAGATCC[C/T]ATCTCTGAAACATAG	9169
rs1012642	snp	C/T	0.472147	0.114677	intron-variant	SCAF11	GRCh38.p7	12:45959496	TTAGAAGGCTGAAGA[C/T]ACTTATTCCTGATCC	9169
rs1047878	snp	A/T			utr-variant-3-prime, intron-variant	SCAF11	GRCh38.p7	12:45921265	gccgggcatgatggc[A/T]cacgcctgtaatccc	9169
rs1062905	snp	A/T	0.417683	0.185425	intron-variant	SCAF11	GRCh38.p7	12:45923221	TTAATGTTATTTCTA[A/T]TGCATCACTAAAAGA	9169
rs1291620	snp	C/T	0.00358779	0.0422022	intron-variant	SCAF11	GRCh38.p7	12:45941841	gggtctgcttattca[C/T]gaatgtttttcaata	9169
rs1291621	snp	A/G	0.0119091	0.0762411	intron-variant	SCAF11	GRCh38.p7	12:45947038	GTGTTATAAATTAGT[A/G]ATAGGTTGAATTAAT	9169
rs1291622	snp	C/G	0.0119091	0.0762411	intron-variant	SCAF11	GRCh38.p7	12:45951300	CTAGCCAATTAAATT[C/G]TTTGAAATATGGGAA	9169
rs1291623	snp	A/T	0.00279162	0.0372561	intron-variant	SCAF11	GRCh38.p7	12:45955636	TTAACTAATACTTAC[A/T]CTATTTTTAAGTTAT	9169
rs1291624	snp	C/G/T	0.5	0	intron-variant	SCAF11	GRCh38.p7	12:45972881	ATATATATATATATA[C/G/T]ATATATATATAGATA	9169
rs1291626	snp	C/T	0	0	utr-variant-3-prime, intron-variant	SCAF11	GRCh38.p7	12:45921655	AAAGATCATACTTTA[C/T]ATTTTAACCTGACAG	9169
rs1291627	snp	A/T	0.0119091	0.0762411	intron-variant	SCAF11	GRCh38.p7	12:45932636	TTAAGTATATATTAT[A/T]TATCTAGCACCATCT	9169
rs1291628	snp	G/T	0.188	0.24219	intron-variant	SCAF11	GRCh38.p7	12:45932793	AAAGCGTGATTCAGC[G/T]GACAGCACGCAGGTA	9169
rs1366023	snp	C/T	0.193028	0.243422	intron-variant	SCAF11	GRCh38.p7	12:45986378	GAGACCAGCAGGCCT[C/T]AGTTAATAGATTGAA	9169
rs1366024	snp	A/G	0.469049	0.120489	utr-variant-3-prime, intron-variant	SCAF11	GRCh38.p7	12:45919855	AACTTGTTTGCAAAA[A/G]CTAAATGGTATAAAA	9169
rs1427749	snp	C/G	0.215446	0.2476	intron-variant	SCAF11	GRCh38.p7	12:45976333	acagtaagatatttt[C/G]agagagcccacattc	9169
rs1549591	snp	G/T	0.209388	0.246679	upstream-variant-2KB	SCAF11	GRCh38.p7	12:45993430	CCTTAATTTGAACTT[G/T]ATATTGTATTCTATT	9169
rs1802104	snp	C/T			synonymous-codon	SCAF11	GRCh38.p7	12:45926827	ATTTGGTAGAATTGA[C/T]AGAGATAGTTACTCT	9169
rs1978598	snp	C/G	0.200182	0.244986	intron-variant	SCAF11	GRCh38.p7	12:45984023	CTTTTAAAGTTTATA[C/G]TTATTCCTTTTTGTA	9169
rs2022104	snp	A/G			intron-variant	SCAF11	GRCh38.p7	12:45972557	ttgctgtcgcatcca[A/G]gctgaagtgcatggc	9169
rs2408438	snp	C/T	0	0	intron-variant	SCAF11	GRCh38.p7	12:45935894	TTTCCTGAAGATCGT[C/T]TCACAAATCCACCCT	9169
rs2408439	snp	C/T			intron-variant	SCAF11	GRCh38.p7	12:45935895	TTCCTGAAGATCGTT[C/T]CACAAATCCACCCTA	9169
rs2408440	snp	C/T			intron-variant	SCAF11	GRCh38.p7	12:45935896	TCCTGAAGATCGTTT[C/T]ACAAATCCACCCTAC	9169
rs2408441	snp	A/G			intron-variant	SCAF11	GRCh38.p7	12:45935897	CCTGAAGATCGTTTC[A/G]CAAATCCACCCTACT	9169
rs2408442	snp	A/G			intron-variant	SCAF11	GRCh38.p7	12:45935900	GAAGATCGTTTCACA[A/G]ATCCACCCTACTTGT	9169
rs2897932	snp	A/C			intron-variant	SCAF11	GRCh38.p7	12:45935898	CTGAAGATCGTTTCA[A/C]AAATCCACCCTACTT	9169
rs4144983	snp	A/G	0.406468	0.194981	intron-variant	SCAF11	GRCh38.p7	12:45976284	TCAACGTCTTGTGTC[A/G]TTCCACCTTCATTTC	9169
rs4768099	snp	G/T	0.204803	0.245881	intron-variant	SCAF11	GRCh38.p7	12:45958639	TGAATTCCTTGAAAC[G/T]AAATATAATCATAGT	9169
rs4768100	snp	A/T	0.417034	0.18601	intron-variant	SCAF11	GRCh38.p7	12:45965191	ATAAGTGAATTTTTT[A/T]AAAAAAGATAGATAC	9169
rs4768670	snp	G/T	0.418169	0.184985	intron-variant	SCAF11	GRCh38.p7	12:45948084	TTTAATTCTTTTTAT[G/T]TTGTGTTATTTTTTA	9169
rs4768671	snp	C/T	0.215446	0.2476	intron-variant	SCAF11	GRCh38.p7	12:45958780	GGATTCTGACATACC[C/T]AAAGACTTTTTACTT	9169
rs5797955	in-del	-/T			intron-variant	SCAF11	GRCh38.p7	12:45969229	ATTTTAACAGTTGCT[-/T]GGGTACCTCAAGCCT	9169
rs5797956	in-del	-/A			upstream-variant-2KB	SCAF11	GRCh38.p7	12:45993793	CAAAAAAAAAAAAAA[-/A]GAAAAAGAAAAAAAA	9169
rs6582578	snp	C/T	0.19459	0.243782	intron-variant	SCAF11	GRCh38.p7	12:45941341	taatgttctgatata[C/T]gtacacattgtgaaa	9169
rs6582580	snp	A/T	0.253264	0.249979	intron-variant	SCAF11	GRCh38.p7	12:45987945	GTCTATGTACTAGGA[A/T]TTCATACATTAAGTT	9169
rs7298703	snp	C/G	0.482609	0.0916147	intron-variant	SCAF11	GRCh38.p7	12:45957610	ATTTTATACAAAATG[C/G]GTGATTTTGTATAAA	9169
rs7306229	snp	C/T	0.474091	0.11083	intron-variant	SCAF11	GRCh38.p7	12:45941049	TTAGTCTTAAACATT[C/T]TGCCTGAACTCAAGA	9169
rs7309711	snp	C/T	0.189261	0.242509	intron-variant	SCAF11	GRCh38.p7	12:45932499	GTTCTGCCATCATTC[C/T]TAGAGGGTGAATGCC	9169
rs7315715	snp	A/G			intron-variant, upstream-variant-2KB	SCAF11	GRCh38.p7	12:45961347	ATAAAACAAAAAGCA[A/G]ACAGAAGGTGTTATT	9169
rs7315731	snp	A/T	0.49644	0.0420383	missense	SCAF11	GRCh38.p7	12:45927731	TCTTGAATATTATTG[A/T]AATCTTCATTCCCAA	9169
rs7964761	snp	C/G	0.0154538	0.0865337	intron-variant	SCAF11	GRCh38.p7	12:45952109	ATTTTAATATTCTAT[C/G]ACTTAATATTTTCCC	9169
rs7965539	snp	A/T	0.192088	0.2432	intron-variant	SCAF11	GRCh38.p7	12:45935781	ATCCAGTTCAAAAGC[A/T]GTTTCACATATTTCT	9169
rs7967208	snp	A/G	0.493568	0.0563433	intron-variant	SCAF11	GRCh38.p7	12:45954293	ctggagtgcagtggc[A/G]ctatcatgggtcact	9169
rs7968005	snp	C/T	0.0107246	0.0724382	intron-variant	SCAF11	GRCh38.p7	12:45948779	CTTATAACAGAGATA[C/T]GAACACAGATTTGTA	9169
rs7968469	snp	C/T	0.0111196	0.0737302	intron-variant	SCAF11	GRCh38.p7	12:45958138	ttaaactcctgggct[C/T]gagtgatccaccctc	9169
rs7971936	snp	G/T	0.253264	0.249979	intron-variant	SCAF11	GRCh38.p7	12:45959342	TAAAAAGATTTTAAC[G/T]TCAGGCTATCCCTTG	9169
rs7972499	snp	G/T	0.19459	0.243782	intron-variant	SCAF11	GRCh38.p7	12:45987482	GCTGATCTCACAGAA[G/T]ATAAATCACAGTGAA	9169
rs7973329	snp	C/T	0.215446	0.2476	intron-variant	SCAF11	GRCh38.p7	12:45987423	ATTCATTAACTTACA[C/T]TGAAGGCATTGTTCA	9169
rs10492249	snp	C/T	0.0150606	0.0854603	downstream-variant-500B	SCAF11	GRCh38.p7	12:45919033	CCATGATGCGAATGA[C/T]TGGTACAAATCCAAG	9169
rs10506264	snp	C/T	0.194902	0.243853	intron-variant	SCAF11	GRCh38.p7	12:45957866	TTTTTAATCACTTCT[C/T]GGCAACTGTGGGAAA	9169
rs10683271	snp	G/T			intron-variant	SCAF11	GRCh38.p7	12:45972901	atatatagatatata[G/T]atatatagatatata	9169
rs10785592	snp	A/G	0.475081	0.108804	intron-variant	SCAF11	GRCh38.p7	12:45984158	TTACCTTAATAAAAA[A/G]AAAAAGGGATTACTT	9169
rs10785593	snp	C/T	0.46865	0.121211	intron-variant	SCAF11	GRCh38.p7	12:45990241	ATTCCGAAACTTTGT[C/T]AGCCCTCGCGTCGCC	9169
rs10785594	snp	C/T	0.468349	0.121752	intron-variant	SCAF11	GRCh38.p7	12:45990247	AAACTTTGTCAGCCC[C/T]CGCGTCGCCCTAGGC	9169
rs10785595	snp	C/T	0.46865	0.121211	intron-variant	SCAF11	GRCh38.p7	12:45990248	AACTTTGTCAGCCCT[C/T]GCGTCGCCCTAGGCC	9169
rs10880867	snp	A/G	0.418007	0.185132	utr-variant-3-prime, intron-variant	SCAF11	GRCh38.p7	12:45920609	AGTATTAAAAAGAGA[A/G]AAAAAAAAAAACCCA	9169
rs10880868	snp	C/T	0.284619	0.247591	synonymous-codon	SCAF11	GRCh38.p7	12:45928666	ACCTGGGGCATCACA[C/T]CCAGAATTGTCTGAT	9169
rs10880869	snp	C/T	0.147321	0.227941	intron-variant	SCAF11	GRCh38.p7	12:45932365	CAATATAAGGTAAGA[C/T]TCTGGAGTAGGAGAA	9169
rs10880870	snp	C/T	0.11275	0.208956	intron-variant	SCAF11	GRCh38.p7	12:45944297	TTTAACCACAGAAGT[C/T]CAGAGATCAAAACAA	9169
rs10880871	snp	C/G	0.47023	0.118317	intron-variant	SCAF11	GRCh38.p7	12:45946955	TCTAGCAGAAGGGAT[C/G]TGAATCATTCTTCAC	9169
rs10880872	snp	C/T	0.197703	0.244469	intron-variant	SCAF11	GRCh38.p7	12:45951196	CACAGTTTTCAGTTA[C/T]TTTGGACTTAAGGTT	9169
rs10880873	snp	C/T	0.416871	0.186156	intron-variant	SCAF11	GRCh38.p7	12:45966041	GGAATATTTCCCACT[C/T]TTAGCCTATGTGTGC	9169
rs10880874	snp	A/T	0.416871	0.186156	intron-variant	SCAF11	GRCh38.p7	12:45966049	TCCCACTCTTAGCCT[A/T]TGTGTGCAACATTAG	9169
rs10880875	snp	C/T	0.470618	0.117591	intron-variant	SCAF11	GRCh38.p7	12:45967236	AAAAAAAAAACAACC[C/T]ACAATTAATATTTTA	9169
rs10880876	snp	A/C			intron-variant	SCAF11	GRCh38.p7	12:45972914	TATATATATAGATAT[A/C]TATATAGATATATAG	9169
rs10880877	snp	G/T	0.0807149	0.183963	intron-variant	SCAF11	GRCh38.p7	12:45972921	ATAGATATATATATA[G/T]ATATATAGATATATA	9169
rs10880878	snp	G/T			intron-variant	SCAF11	GRCh38.p7	12:45972929	ATATATAGATATATA[G/T]ATATATATAGATATA	9169
rs10880879	snp	C/T	0.483199	0.0901004	intron-variant	SCAF11	GRCh38.p7	12:45974120	GTATATATGTTTATA[C/T]TATACTGTAGTCCAT	9169
rs10880880	snp	A/G	0.470618	0.117591	intron-variant	SCAF11	GRCh38.p7	12:45981523	TTCTCCCATTTTCTG[A/G]GGAATAAATATAATC	9169
rs10880881	snp	C/T	0	0	intron-variant	SCAF11	GRCh38.p7	12:45985299	TTGATCAACCCCCTG[C/T]ATGTGGCCAGTTTCC	9169
rs11183237	snp	A/T	0.0107246	0.0724382	utr-variant-3-prime, intron-variant	SCAF11	GRCh38.p7	12:45920014	GCACACCTCCTTAGT[A/T]GTTTTAGATTAGAAC	9169
rs11183240	snp	A/C	0.0460142	0.144533	intron-variant	SCAF11	GRCh38.p7	12:45932291	CATTCAAACCCAAAC[A/C]ACTTCTTGGCTTTCT	9169
rs11183241	snp	C/T	0.493154	0.0581045	intron-variant	SCAF11	GRCh38.p7	12:45936415	CCAAAGTGCTGGGAT[C/T]ACAGGCATGAGCCAC	9169
rs11183242	snp	C/T	0.0463947	0.145069	intron-variant	SCAF11	GRCh38.p7	12:45938357	AGCCGGGCATGATGG[C/T]GGGCACCTGTAATCC	9169
rs11183243	snp	A/G	0.474634	0.109726	intron-variant	SCAF11	GRCh38.p7	12:45942475	AATGTACCAGATCAC[A/G]TTACTCCTGAAAACA	9169
rs11183244	snp	C/T	0.00636936	0.0560724	intron-variant	SCAF11	GRCh38.p7	12:45944976	AATAAGGCCACAGTA[C/T]GAGCTGGTCAACACC	9169
rs11183245	snp	C/T	0.0078325	0.0620878	synonymous-codon	SCAF11	GRCh38.p7	12:45945250	CTTGAAGTGGATACA[C/T]AGTAAGTTACTTTTT	9169
rs11183246	snp	A/G			intron-variant	SCAF11	GRCh38.p7	12:45954769	TTAACTTTTTTCATA[A/G]AGACAGGGTCTCACT	9169
rs11183247	snp	G/T	0.00478085	0.0486577	intron-variant	SCAF11	GRCh38.p7	12:45959776	AATTTATTAATAGAT[G/T]GCTCTCTTGTTACTG	9169
rs11183248	snp	A/G	0.195214	0.243923	intron-variant, upstream-variant-2KB	SCAF11	GRCh38.p7	12:45960850	ATTAGCTGCATTCCA[A/G]TTGTTAATGTTCTTA	9169
rs11183249	snp	C/T	0.0463947	0.145069	intron-variant, upstream-variant-2KB	SCAF11	GRCh38.p7	12:45961154	ACAggaattagaaaa[C/T]cagttctaaattcac	9169
rs11183250	snp	A/T	0.0460142	0.144533	intron-variant, upstream-variant-2KB	SCAF11	GRCh38.p7	12:45961483	TTATTAACTTTTTTT[A/T]AAAAAGTATGCATTT	9169
rs11183251	snp	A/G	0.406296	0.19512	intron-variant	SCAF11	GRCh38.p7	12:45962868	TGATAAATTAAATCT[A/G]TGAGGGCCTAATTTA	9169
rs11183253	snp	C/T	0.00438332	0.0466095	intron-variant	SCAF11	GRCh38.p7	12:45968255	ATTTTCAGTAAACTT[C/T]GCTTTTCTGATTATT	9169
rs11183254	snp	A/C			intron-variant	SCAF11	GRCh38.p7	12:45972856	AAAGCCAGTATATAT[A/C]TATATATCGATATAT	9169
rs11183255	snp	G/T			intron-variant	SCAF11	GRCh38.p7	12:45972857	AAGCCAGTATATATA[G/T]ATATATCGATATATA	9169
rs11183256	snp	A/C			intron-variant	SCAF11	GRCh38.p7	12:45972864	TATATATATATATAT[A/C]GATATATATATATAT	9169
rs11183257	snp	G/T			intron-variant	SCAF11	GRCh38.p7	12:45972865	ATATATATATATATC[G/T]ATATATATATATATA	9169
rs11183258	snp	G/T			intron-variant	SCAF11	GRCh38.p7	12:45972873	ATATATCGATATATA[G/T]ATATATAGATATATA	9169
rs11183259	snp	G/T			intron-variant	SCAF11	GRCh38.p7	12:45972885	ATATATATATAGATA[G/T]ATATATAGATATATA	9169
rs11183260	snp	G/T			intron-variant	SCAF11	GRCh38.p7	12:45972893	ATAGATATATATATA[G/T]ATATATATATATATA	9169
rs11183261	snp	G/T			intron-variant	SCAF11	GRCh38.p7	12:45972903	ATATAGATATATATA[G/T]ATATAGATATATATA	9169
rs11183262	snp	G/T	0.444444	0.157135	intron-variant	SCAF11	GRCh38.p7	12:45972915	ATATATATAGATATA[G/T]ATATAGATATATAGA	9169
rs11183263	snp	G/T			intron-variant	SCAF11	GRCh38.p7	12:45972919	ATATAGATATATATA[G/T]AGATATATAGATATA	9169
rs11183264	snp	G/T			intron-variant	SCAF11	GRCh38.p7	12:45972923	AGATATATATATAGA[G/T]ATATAGATATATATA	9169
rs11183265	snp	G/T			intron-variant	SCAF11	GRCh38.p7	12:45972931	ATATAGATATATAGA[G/T]ATATATAGATATATA	9169
rs11183266	snp	G/T			intron-variant	SCAF11	GRCh38.p7	12:45972935	AGATATATAGATATA[G/T]ATAGATATATATATA	9169

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