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
rs1054108	snp	C/T	0	0	utr-variant-3-prime	TRIM55	GRCh38.p7	8:66174731	AATAGCCCCAAACTG[C/T]AATTCCATATGACTT	84675
rs2357669	snp	C/G	0.0948562	0.196037	intron-variant	TRIM55	GRCh38.p7	8:66127704	gctgggcatggtggc[C/G]ggcacctataatctc	84675
rs2357670	snp	C/G	0	0	intron-variant	TRIM55	GRCh38.p7	8:66137384	CATGAGTCACTGAGG[C/G]AGATGTTACCACAAT	84675
rs2357671	snp	A/T	0.399611	0.200291	intron-variant	TRIM55	GRCh38.p7	8:66138784	ATCATGGTACCTATC[A/T]TATAGAGTTACTATG	84675
rs2446433	snp	A/G	0.0364509	0.129988	intron-variant	TRIM55	GRCh38.p7	8:66155896	AGCAATTCTCCTCAG[A/G]AAGAGGTCTTGAGGC	84675
rs2469280	snp	A/T	0	0	intron-variant	TRIM55	GRCh38.p7	8:66131265	AACATACACAACTTT[A/T]AGAATTCATTACTAC	84675
rs2469281	snp	A/C	0	0	intron-variant	TRIM55	GRCh38.p7	8:66137755	TGGCACATAATCAAC[A/C]CTGAAAAAAAAAAAA	84675
rs2884229	snp	A/C	0.0240643	0.107019	intron-variant	TRIM55	GRCh38.p7	8:66148286	GATGGTACTGGAGAT[A/C]CTTCAGCCACACAAC	84675
rs3739333	snp	A/T			upstream-variant-2KB	TRIM55	GRCh38.p7	8:66111146	TTTTCCATGTTGCAA[A/T]AGATTTTTTTTCTTT	84675
rs3924870	snp	A/G			intron-variant	TRIM55	GRCh38.p7	8:66116515	gggagggtaaggtag[A/G]aggatctcttgaacc	84675
rs4299985	snp	C/G	0	0	intron-variant	TRIM55	GRCh38.p7	8:66118023	ATACAAAAAAACTTA[C/G]CCGGGTGTGGTGGCG	84675
rs4317551	snp	A/C	0	0	intron-variant	TRIM55	GRCh38.p7	8:66117966	GATCAGGAGATCGAG[A/C]CCATCCTGGCTAACA	84675
rs4348478	snp	C/G	0.0448719	0.142907	intron-variant	TRIM55	GRCh38.p7	8:66118304	AGAAGGAGTGATTAT[C/G]AAATGAACAAAAGAT	84675
rs4366069	snp	A/G	0.354019	0.227333	intron-variant	TRIM55	GRCh38.p7	8:66133639	TGAAACTGGAAGTCC[A/G]TGCAATTTTCTTACA	84675
rs4434604	snp	A/G	0.0451921	0.143366	synonymous-codon, intron-variant, splice-acceptor-variant	TRIM55	GRCh38.p7	8:66152378	CCTTACCTTACCAGA[A/G]GATGAAGATGAAGAA	84675
rs4477003	snp	C/G	0	0	intron-variant	TRIM55	GRCh38.p7	8:66118042	GGTGTGGTGGCGGGC[C/G]CCTGTAGTCCCAGCT	84675
rs4737766	snp	A/G	0.031825	0.122064	intron-variant	TRIM55	GRCh38.p7	8:66141206	CATGAATTTACTGTG[A/G]TAATGAAGAAGGATT	84675
rs4737767	snp	C/T	0.0433465	0.140692	intron-variant	TRIM55	GRCh38.p7	8:66159984	gtctgtggctttccc[C/T]ttcatttcttttaat	84675
rs6472251	snp	A/G	0.354235	0.227234	upstream-variant-2KB, intron-variant	TRIM55	GRCh38.p7	8:66125699	ATTGAAAGGACTAAG[A/G]TAATTCTCTAAAGAT	84675
rs6472252	snp	C/G	0.263535	0.249633	intron-variant	TRIM55	GRCh38.p7	8:66144700	AGAGGGGAGGTGTAT[C/G]GCTCCGAATTGGTCT	84675
rs6472253	snp	C/T	0.0955749	0.196603	intron-variant	TRIM55	GRCh38.p7	8:66145635	CTTTAAAAAATCTAC[C/T]TTAAGCATAGTGAAT	84675
rs6472254	snp	C/T	0.335788	0.23482	intron-variant	TRIM55	GRCh38.p7	8:66153061	GAAATAAATAGCATA[C/T]AGAGTAAGAAATAAA	84675
rs6472255	snp	A/T	0.336474	0.234568	intron-variant	TRIM55	GRCh38.p7	8:66162905	gatcattttgttaat[A/T]tttgtgtagatgaga	84675
rs6472256	snp	A/G	0.336474	0.234568	intron-variant	TRIM55	GRCh38.p7	8:66162920	atttgtgtagatgag[A/G]taaggatcaaagttt	84675
rs6982063	snp	A/G	0.0193772	0.0965046	intron-variant	TRIM55	GRCh38.p7	8:66153237	TTCTATGGATTTGTC[A/G]TTTGATGAGATTGTG	84675
rs6986947	snp	C/T	0.154329	0.23097	intron-variant	TRIM55	GRCh38.p7	8:66115842	cttttaattaagata[C/T]aacatgtaaaggcct	84675
rs6988195	snp	A/T	0.35445	0.227135	upstream-variant-2KB	TRIM55	GRCh38.p7	8:66110674	CTGTGTCCTGCGGAC[A/T]ATCAGGCTTTGCATT	84675
rs6990486	snp	A/G	0.146314	0.227484	intron-variant	TRIM55	GRCh38.p7	8:66172845	ATCCAGGCGGAATTC[A/G]CTATTTGCTCAAATT	84675
rs6990624	snp	C/G	0.336474	0.234568	intron-variant	TRIM55	GRCh38.p7	8:66165856	TGTAGGAGAGGGTAA[C/G]ATTTTTTTAACAAGT	84675
rs6996265	snp	A/G	0.336474	0.234568	intron-variant	TRIM55	GRCh38.p7	8:66174115	CCCTTTCTAAACCCA[A/G]TTCCTAGAGGTTTCA	84675
rs6998258	snp	A/G	0.121369	0.214369	utr-variant-5-prime, intron-variant, upstream-variant-2KB	TRIM55	GRCh38.p7	8:66127154	ACAATGTCCTCCACC[A/G]AGAGAAACGTAAAGG	84675
rs6998761	snp	A/G	0.335559	0.234904	intron-variant	TRIM55	GRCh38.p7	8:66149402	AAGAACAGAAGATTG[A/G]AAAACCATTGATTCA	84675
rs6999100	snp	C/T	0.477345	0.103991	intron-variant	TRIM55	GRCh38.p7	8:66170497	gacattttgtttatc[C/T]gcttctccaaggatg	84675
rs7006903	snp	A/G	0.266	0.249487	upstream-variant-2KB	TRIM55	GRCh38.p7	8:66110924	AAAAAATTCAGCAAC[A/G]GCTGCACAACATTGT	84675
rs7008138	snp	A/C	0.0629771	0.165899	intron-variant	TRIM55	GRCh38.p7	8:66128851	AAAGCAAAGAAAAAA[A/C]AATCTAGTAAATACT	84675
rs7008578	snp	A/G	0.354019	0.227333	intron-variant	TRIM55	GRCh38.p7	8:66129150	TGTTGATTGTGAATA[A/G]CATCGTGATAGCATT	84675
rs7010547	snp	G/T	0.184203	0.241186	intron-variant	TRIM55	GRCh38.p7	8:66172934	TTTGTTGTTGTTGTT[G/T]TTTGCATAAGCCATA	84675
rs7350113	snp	C/T	0.0189856	0.0955633	intron-variant	TRIM55	GRCh38.p7	8:66167360	TAATTCTTCACAATC[C/T]AGTTCTTTTTTCAGG	84675
rs7460583	snp	C/G	0	0	intron-variant	TRIM55	GRCh38.p7	8:66119355	TGCTTCAAACCATAT[C/G]GGTTTTTTATTTCCT	84675
rs7818902	snp	A/T	0.335559	0.234904	intron-variant	TRIM55	GRCh38.p7	8:66151143	TAGGAGGCATGTGGG[A/T]TAGATATTGCAGCAC	84675
rs7820617	snp	C/T	0.273318	0.24891	intron-variant	TRIM55	GRCh38.p7	8:66163310	tttcttcattgtgct[C/T]actttgggtttaatt	84675
rs7822243	snp	C/T	0.335788	0.23482	intron-variant	TRIM55	GRCh38.p7	8:66157153	CATGCTTCAAGGCTG[C/T]GATCCACTGAGCCCA	84675
rs7825257	snp	A/C	0.474903	0.109173	intron-variant	TRIM55	GRCh38.p7	8:66138330	ATTTTATAAATGGTA[A/C]TATGTGGTATTTTTC	84675
rs7826464	snp	C/T	0.336474	0.234568	intron-variant	TRIM55	GRCh38.p7	8:66157662	AGGCTCACTTGCTGA[C/T]CTGTAAACTACATTC	84675
rs7827407	snp	A/G	0.336474	0.234568	intron-variant	TRIM55	GRCh38.p7	8:66161557	cttttttctagttct[A/G]tgaagaatgatggtg	84675
rs7827692	snp	A/C	0.0256215	0.110247	intron-variant	TRIM55	GRCh38.p7	8:66161740	ttcatgtccttggtt[A/C]ggtatattcctaagg	84675
rs7828111	snp	C/G	0.273049	0.248935	intron-variant	TRIM55	GRCh38.p7	8:66161776	tttttttttttgcaa[C/G]tattgtgaaaggggt	84675
rs7830926	snp	C/T	0.333261	0.235728	intron-variant	TRIM55	GRCh38.p7	8:66139876	TCATATATAACAGTA[C/T]AGAAAGTAcagtcat	84675
rs7831234	snp	A/G	0.270892	0.249126	intron-variant	TRIM55	GRCh38.p7	8:66140160	tgtgatgctcacaca[A/G]tggaactgcctaagg	84675
rs7832842	snp	A/G	0.0509478	0.151255	intron-variant	TRIM55	GRCh38.p7	8:66155460	TTCTTATACATGGTA[A/G]TAGAAGCTGTGTGCG	84675
rs7834423	snp	C/T	0.354235	0.227234	intron-variant	TRIM55	GRCh38.p7	8:66123067	tctgaagcctgctac[C/T]cggaagcttcttctg	84675
rs7834526	snp	C/G	0.0955749	0.196603	intron-variant	TRIM55	GRCh38.p7	8:66150807	gagtagctgggatta[C/G]aggcacctgccacca	84675
rs7835214	snp	C/T	0.271432	0.24908	intron-variant	TRIM55	GRCh38.p7	8:66172144	GTGTAAAGTGCTTTA[C/T]GTGTATTACTTTATT	84675
rs7835340	snp	A/G	0.336017	0.234736	intron-variant	TRIM55	GRCh38.p7	8:66140334	CACTGCCTCCCTTAT[A/G]TATTCCTGTATTCAC	84675
rs7835948	snp	C/T	0.350327	0.228986	intron-variant	TRIM55	GRCh38.p7	8:66131808	gtaacagaactaaga[C/T]gcaactcaagtaggt	84675
rs7838125	snp	C/T	0.264632	0.249571	intron-variant	TRIM55	GRCh38.p7	8:66123299	tgatgtcttatgtct[C/T]cctgaaacttataaa	84675
rs7838500	snp	A/G	0.335559	0.234904	intron-variant	TRIM55	GRCh38.p7	8:66151294	ACCTTTTGGCCCAGA[A/G]GTCCCATTTCTGAAA	84675
rs7838582	snp	C/T	0.153997	0.230832	intron-variant	TRIM55	GRCh38.p7	8:66114446	TTAGACCCATTTAAT[C/T]GGGGGGAAATTCACG	84675
rs7839635	snp	G/T	0.121022	0.21416	intron-variant	TRIM55	GRCh38.p7	8:66138039	TCCAGGCCCTGGCTC[G/T]GTAACTGGAGCAGTC	84675
rs7840087	snp	A/G	0.0295035	0.117819	intron-variant	TRIM55	GRCh38.p7	8:66141339	ACCTCCGCTTCTTGA[A/G]AGTGGCTTGGCCTAA	84675
rs7841890	snp	A/G	0.0509478	0.151255	intron-variant	TRIM55	GRCh38.p7	8:66157294	AGTTCTTGGTGTTTG[A/G]GGAAGGGCCTTTCAC	84675
rs7842707	snp	A/G	0.335788	0.23482	intron-variant	TRIM55	GRCh38.p7	8:66157538	CTAGGCTTACCTTGA[A/G]TATTTAGGATGTGGT	84675
rs7842761	snp	C/T	0.336474	0.234568	intron-variant	TRIM55	GRCh38.p7	8:66157743	CTGGTGCTTTCCTTA[C/T]ATCCATGTACACAGT	84675
rs7843038	snp	C/T	0.273049	0.248935	intron-variant	TRIM55	GRCh38.p7	8:66157920	TGATGGACAGGACCA[C/T]TACTTTTTGTTAGAT	84675
rs7843077	snp	C/T	0.482008	0.0931261	intron-variant	TRIM55	GRCh38.p7	8:66124338	CTTCCTGCTGCTTAA[C/T]TTATTAAGTGTTAAA	84675
rs7843605	snp	A/G	0.242285	0.249881	missense, intron-variant	TRIM55	GRCh38.p7	8:66152419	GCGGAGAAGGAGAAA[A/G]AGAAGGAGAAGGAGA	84675
rs7844591	snp	A/G	0.0182019	0.0936463	intron-variant	TRIM55	GRCh38.p7	8:66145653	AAGCATAGTGAATTT[A/G]GGttttgtttttttt	84675
rs7845017	snp	A/G	0.143284	0.226079	intron-variant	TRIM55	GRCh38.p7	8:66145986	cttgagaaagtgaca[A/G]ctctgctgggtttca	84675
rs7845334	snp	A/G	0.35445	0.227135	upstream-variant-2KB	TRIM55	GRCh38.p7	8:66112601	AAAGACATTCTATGT[A/G]ATCTTCTTCCCTCTC	84675
rs7846184	snp	C/G	0.26271	0.249677	upstream-variant-2KB, intron-variant	TRIM55	GRCh38.p7	8:66113119	AAAAGTACGACAAGG[C/G]GGGGCGGTGGAATCG	84675
rs9643575	snp	A/C	0.39979	0.200158	intron-variant	TRIM55	GRCh38.p7	8:66140081	TGTCCTAGGAGCAAT[A/C]GATTGTGCTATACAA	84675
rs9694082	snp	C/G	0.335788	0.23482	intron-variant	TRIM55	GRCh38.p7	8:66154545	ATTTGAGTTCACTCT[C/G]CTGGTGCATGGTGAC	84675
rs10092687	snp	C/T	0.353371	0.227628	intron-variant	TRIM55	GRCh38.p7	8:66132841	AGGAATATGGGAAAT[C/T]GTTCTCAGTGTATAC	84675
rs10093091	snp	A/G	0.336474	0.234568	intron-variant	TRIM55	GRCh38.p7	8:66170016	TGTGTTTCTTTAGGA[A/G]CCAAGAAGGTAACAT	84675
rs10093753	snp	A/G	0.0901694	0.192235	intron-variant	TRIM55	GRCh38.p7	8:66164358	TTGTCACTGTTCTGT[A/G]GGGCTCTATTTTTAG	84675
rs10099957	snp	A/G	0.270892	0.249126	intron-variant	TRIM55	GRCh38.p7	8:66143295	CACGTGTGCAAGCTA[A/G]TGCTGAGCTTTCAGG	84675
rs10101457	snp	A/G	0.353587	0.22753	intron-variant	TRIM55	GRCh38.p7	8:66131282	gaattcattactact[A/G]ggcctctgaagagaa	84675
rs10104916	snp	G/T	0.335559	0.234904	intron-variant	TRIM55	GRCh38.p7	8:66156427	CATCAAGCAGTCCAT[G/T]TATATTATTTCCGAG	84675
rs10105164	snp	C/T	0.198014	0.244535	intron-variant	TRIM55	GRCh38.p7	8:66173032	AAGGAAGGAGTTGGA[C/T]GTGTAAAAATAGGTG	84675
rs10107870	snp	A/T	0.303438	0.244222	intron-variant	TRIM55	GRCh38.p7	8:66169896	TTGCCTGAATTTTTT[A/T]AAAATTTTTTATTCT	84675
rs10109602	snp	A/C	0.271432	0.24908	intron-variant	TRIM55	GRCh38.p7	8:66133743	ATTAGCGTCTTACAG[A/C]GGCACATCAGCACGT	84675
rs10109794	snp	G/T	0.117886	0.21224	intron-variant	TRIM55	GRCh38.p7	8:66133702	TCTCAAGTAATTGAC[G/T]TCCACCTAGCAACTT	84675
rs10112988	snp	A/G	0.130351	0.219509	intron-variant	TRIM55	GRCh38.p7	8:66167950	gggtggggtcatgcc[A/G]tattgcccaggctgg	84675
rs10113208	snp	C/T	0.296619	0.245615	intron-variant	TRIM55	GRCh38.p7	8:66134480	GAGGCTGGAGGGGGG[C/T]GATCTAGCTACTCCT	84675
rs10113256	snp	A/G	0.0898077	0.191933	intron-variant	TRIM55	GRCh38.p7	8:66167934	taaaagttttttgta[A/G]gggtggggtcatgcc	84675
rs10630107	in-del	-/GGGTC	0.477004	0.104734	intron-variant	TRIM55	GRCh38.p7	8:66171970	GTCTTTTCTTATTGG[-/GGGTC]GGTGCTATTGTATAT	84675
rs10957366	snp	C/G	0.482459	0.0919928	intron-variant	TRIM55	GRCh38.p7	8:66117705	ATCAGTTAAGAGGGT[C/G]GGGTGGAGGAGAAGT	84675
rs10957367	snp	A/C	0.251296	0.249997	intron-variant	TRIM55	GRCh38.p7	8:66147813	aaaaaaaaaaaaaaa[A/C]aaaaCCACAAAATCT	84675
rs10957368	snp	G/T	0.129664	0.219133	intron-variant	TRIM55	GRCh38.p7	8:66173067	ATTCTGTCAGGATAA[G/T]GTTTATTTTACTTCA	84675
rs11409958	in-del	-/G	0.354881	0.226936	upstream-variant-2KB	TRIM55	GRCh38.p7	8:66112552	GGATTGAATAACTTT[-/G]TTAAAATTAAACATA	84675
rs11455977	in-del	-/C			intron-variant	TRIM55	GRCh38.p7	8:66114082	CTCGAAGGAGAGACA[-/C]CCCCCCCCCCCATTA	84675
rs11780171	snp	C/G	0.289683	0.24683	intron-variant	TRIM55	GRCh38.p7	8:66122196	GCTAAAGGGAAAAGT[C/G]AAGCTGGGAACTGTT	84675
rs11782822	snp	C/T	0	0	intron-variant	TRIM55	GRCh38.p7	8:66165165	AATATTCATATTTTC[C/T]TAAGCCAGGATGGAC	84675
rs11985436	snp	C/T	0.0509478	0.151255	intron-variant	TRIM55	GRCh38.p7	8:66156439	CATTTATATTATTTC[C/T]GAGTCACCGTTCTCA	84675
rs11985860	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM55	GRCh38.p7	8:66151716	gggcgtggtggcgta[C/T]gcctgtaatcccagc	84675
rs11986216	snp	A/G	0.333261	0.235728	intron-variant	TRIM55	GRCh38.p7	8:66141924	ATGAATATAATTAGA[A/G]TTGTTTAAATACCAT	84675
rs11986805	snp	A/G	0.354019	0.227333	intron-variant	TRIM55	GRCh38.p7	8:66124865	cttatcttcacaggc[A/G]tggtacgaaggacag	84675
rs11986876	snp	A/G	0.0452528	0.143452	downstream-variant-500B	TRIM55	GRCh38.p7	8:66175587	TGCATCTTCATACAG[A/G]CAAATTAATTTTGAA	84675
rs11987000	snp	C/T	0.135484	0.22223	intron-variant	TRIM55	GRCh38.p7	8:66118155	gcctgggggacagag[C/T]gagactccgtctcaa	84675
rs11988053	snp	G/T	0.354019	0.227333	upstream-variant-2KB, intron-variant, utr-variant-5-prime	TRIM55	GRCh38.p7	8:66113265	GCTCTGGGGCTCTGC[G/T]CTCCTCGGATTACGC	84675

Full records

It may take some time, please wait.