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
rs10606	snp	A/G	0.303741	0.244155	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456601	CGGCACGCGCCTTCC[A/G]GTGCCAGTGGTGGAC	10612
rs1057364	snp	C/T	0	0	intron-variant	TRIM3	GRCh38.p7	11:6471558	CTGAAGGACCTGGCC[C/T]ACAGTGTGCCCAGAG	10612
rs1060067	snp	C/T			missense, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458091	GTGGCTGGCCGCCCT[C/T]TCTCCTGCCCCAACC	10612
rs1060069	snp	C/G/T	0.00321672	0.0399767	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456787	GGTGCTCAATCTGGG[C/G/T]GCACTGCTCACCACG	10612
rs1060070	snp	A/G	0	0	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456687	TCGCTCACTGTCACT[A/G]CCAAAGACAAGGACG	10612
rs1137113	snp	C/T			synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465638	ATGGACAAGCAGTTC[C/T]TGGTATGCAGCATCT	10612
rs1137114	snp	C/G			missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457019	AGAAGGTGTTGCAAA[C/G]CCAGCTGGACACACT	10612
rs2303491	snp	A/C	0.209084	0.246629	intron-variant	TRIM3	GRCh38.p7	11:6457151	GTAGGTGCTGTGGGC[A/C]TCTGTGTCCTCTGTC	10612
rs2306897	snp	A/C/T	0.000133129	0.00815776	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450903	ATACCTGCAAAGTGG[A/C/T]GGTCAGTGGCCCCAC	10612
rs2344827	snp	A/G	0.295088	0.245901	intron-variant	TRIM3	GRCh38.p7	11:6464439	ctgattctccaaacT[A/G]TAACAGATTCCATAT	10612
rs2555165	snp	C/T	0.0248432	0.108648			GRCh38.p7	11:6474145	ATCCGGCTCGCCGGC[C/T]CGCCGGCTCCCTAGC	10612
rs2555166	snp	C/T					GRCh38.p7	11:6461190	CActgggcatggtgg[C/T]tcatgcctgtaatcc	10612
rs2555167	snp	A/G	0.015066	0.0854751			GRCh38.p7	11:6457891	GGAGGGGACAAAGAA[A/G]TGTGATGTCTAGCCA	10612
rs2634204	snp	C/T	0.0418186	0.138422	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449991	GACTCCCCATAGCTC[C/T]TGGGAGGAGAGCAAG	10612
rs2723617	snp	A/G	0.0441095	0.141807	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475297	ACTGGAGCATCTTGT[A/G]CTATGTGCTGAACTC	10612
rs2723627	snp	A/G	0.0256215	0.110247	intron-variant	TRIM3	GRCh38.p7	11:6464944	gtgagccgagatcgt[A/G]ccactacactccacc	10612
rs2723628	snp	A/G	0	0	intron-variant	TRIM3	GRCh38.p7	11:6465061	catacccaatgccta[A/G]aacagggtctggcac	10612
rs2723630	snp	C/T	0.0414363	0.137845	intron-variant	TRIM3	GRCh38.p7	11:6468309	gtacaatgtgtctct[C/T]tgatgtccaggtaga	10612
rs2723634	snp	C/G	0.0256215	0.110247	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473239	ACAGGAGAACCAGAG[C/G]GGTCCTTTCCTACAA	10612
rs2723636	snp	C/T	0.445893	0.155325	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448827	TGGTGACTGGGTGAG[C/T]CTGGACTGTGGTCCC	10612
rs2723637	snp	A/G	0.209084	0.246629	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448352	GCTGGGAAGGATTGT[A/G]GGGTTGGGGGGGTGA	10612
rs2723647	snp	C/T	0.456332	0.141164	intron-variant	TRIM3	GRCh38.p7	11:6458833	ACTTGTCAGGGGTCA[C/T]ACAGTATAACAGGTG	10612
rs2723650	snp	C/T	0.00398564	0.0444627	intron-variant	TRIM3	GRCh38.p7	11:6453647	TTATCAGCTCTTCTG[C/T]GAAAACTCCCTCATT	10612
rs2723663	snp	A/C	0.499598	0.0141716	intron-variant	TRIM3	GRCh38.p7	11:6462280	tgcccactagaacat[A/C]ctctgagagcaggga	10612
rs2859516	snp	C/T			intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473349	cgccccTTCCATCCT[C/T]TGGTACCCACAGGCC	10612
rs3830325	in-del	-/G			intron-variant	TRIM3	GRCh38.p7	11:6451243	CAGCTGGACACCAGG[-/G]TAAGTAAAGTGACAG	10612
rs4758106	snp	C/G	0.498182	0.0300969	intron-variant	TRIM3	GRCh38.p7	11:6461483	cttccattacccccc[C/G]caccactctgccatc	10612
rs4758419	snp	C/G	0.298905	0.24517	intron-variant	TRIM3	GRCh38.p7	11:6466871	TGCTGTAATGTTCTT[C/G]TTACTTCTCTGCTTT	10612
rs7123791	snp	C/T	0.0908922	0.192833	intron-variant	TRIM3	GRCh38.p7	11:6472770	GAGACCTCTGCTTAA[C/T]ATAAGGAAGCTTTTC	10612
rs7129720	snp	C/T	0.0256215	0.110247	intron-variant	TRIM3	GRCh38.p7	11:6453973	GGCTCCTAGCAGTGG[C/T]GACATAGAGGGCAGG	10612
rs7932604	snp	C/T	0.0539704	0.155153	intron-variant	TRIM3	GRCh38.p7	11:6452338	CTAAGCTTTCTGGCT[C/T]TTCCTTCATAGTCAA	10612
rs7933690	snp	A/G	0.0119091	0.0762411	intron-variant	TRIM3	GRCh38.p7	11:6453478	cttcagggatctcac[A/G]gtctagtgggggaga	10612
rs7936920	snp	A/G	0.480618	0.0965156	intron-variant	TRIM3	GRCh38.p7	11:6453870	GAGAGGAGGAGGGGG[A/G]TCAGACCTCATCAGG	10612
rs7945770	snp	A/G/T	0.0670712	0.171961	intron-variant	TRIM3	GRCh38.p7	11:6452762	AAGGTACAGTTTAGC[A/G/T]GTGAGGTAATGCCCC	10612
rs7950251	snp	A/G	0.144632	0.226711	intron-variant	TRIM3	GRCh38.p7	11:6454097	CTGAAACAATGGGGA[A/G]gccaggtgcagtggc	10612
rs10128723	snp	A/C	0.00486615	0.0490856	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456833	TCCACCTCAAGGACC[A/C]GTTCCAGCTGTGCAT	10612
rs10665333	in-del	-/A/AA/AAA	0	0	intron-variant	TRIM3	GRCh38.p7	11:6454403	AAAAAAAAAAAAAAA[-/A/AA/AAA]CTATGAGGAAGTTCA	10612
rs10839566	snp	A/G	0.469544	0.119585	intron-variant	TRIM3	GRCh38.p7	11:6463257	AAATTAAAATGAAAA[A/G]TTACATTAAAAAATT	10612
rs11040895	snp	G/T	0	0	intron-variant	TRIM3	GRCh38.p7	11:6457501	GAATATCTCATTCCA[G/T]AGTTGCTGAGGGTGG	10612
rs11040896	snp	A/G	0.469642	0.119404	intron-variant	TRIM3	GRCh38.p7	11:6463049	ATCTCTACTAAAAAT[A/G]CAAAAATTAACCGGA	10612
rs11040897	snp	A/G	0.299916	0.244966	intron-variant	TRIM3	GRCh38.p7	11:6463078	GATGTGGTGGCGTGC[A/G]CCTGTAGTCCCAGCT	10612
rs11601210	snp	C/G	0.287085	0.247234	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475447	TTTCTCAACTCTATA[C/G]TTCTCCCATGCAGTC	10612
rs11601975	snp	C/T	0.285257	0.247501	intron-variant	TRIM3	GRCh38.p7	11:6471486	CAATGAAATTCATGG[C/T]CATCTCCCCCAACAT	10612
rs11603021	snp	A/G	0.284471	0.247612	intron-variant	TRIM3	GRCh38.p7	11:6463881	CTTGAATGGACAGGA[A/G]AACTGAGGCCATTTC	10612
rs11603308	snp	A/G	0.315516	0.241263	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475103	TTCCAGAGGTGGGGA[A/G]AATCCTGAAAAATTC	10612
rs11605141	snp	C/T	0.305436	0.243776	intron-variant	TRIM3	GRCh38.p7	11:6457154	AGAGGACACAGATGC[C/T]CACAGCACCTACCGA	10612
rs11605777	snp	C/T	0.473909	0.111197	intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473556	AACCCCGCGCTCCCC[C/T]AAGGAACCATCACCC	10612
rs11605881	snp	A/G	0.286303	0.24735	intron-variant, utr-variant-5-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474370	GGAATATGCTAGTCT[A/G]TCGGCTGACCAGGAA	10612
rs11607223	snp	C/G	0.264358	0.249587	intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473678	CGCCTCACGTGGGCA[C/G]AGAGAGGCACAGCTT	10612
rs11607224	snp	A/G	0.264358	0.249587	intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473685	CGTGGGCAGAGAGAG[A/G]CACAGCTTTTGAAAA	10612
rs11821001	snp	C/G	0.0111196	0.0737302	intron-variant	TRIM3	GRCh38.p7	11:6452423	ACACAAGATGAACGA[C/G]AGCCAGGAGCAGCCT	10612
rs12280082	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6461090	tttgtatttttagta[A/G]agatggggttttgtc	10612
rs12294726	snp	C/G	0.309648	0.24278	intron-variant, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474634	AAGTGGAAAATAATT[C/G]TAACAGTTTACAGGG	10612
rs12419488	snp	A/G	0.02016	0.0983543	intron-variant	TRIM3	GRCh38.p7	11:6467864	actctggcaagctgt[A/G]agaattgaagacaaa	10612
rs12790018	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6463212	tctgtctcaaaaaaa[A/C]aaaaacaaaaacaaa	10612
rs12790725	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6463225	aacaaaaacaaaaac[A/C]aaaaacaaaCCaaaa	10612
rs12807424	snp	A/T	0.0314385	0.121371	intron-variant	TRIM3	GRCh38.p7	11:6461980	atttcacctcatccc[A/T]ctttactcctcactt	10612
rs13343175	snp	C/T	0.306683	0.243489	intron-variant	TRIM3	GRCh38.p7	11:6456225	TCATTCAGAGGTCAT[C/T]TTGAACCTCCCTTCC	10612
rs16913704	snp	C/T	0.0425829	0.139564	intron-variant	TRIM3	GRCh38.p7	11:6452623	CTACTAAGCTCTTCT[C/T]TGGCTGACCAGCACA	10612
rs16913732	snp	A/T	0.32627	0.238082	intron-variant	TRIM3	GRCh38.p7	11:6454709	TAGAAATAGGGTAGG[A/T]GTAAAGGACGACTGG	10612
rs16913748	snp	A/G	0.302114	0.244508	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457389	CTCGAACGCTGCACT[A/G]ATCTGGGCCAGGGCC	10612
rs17821052	snp	G/T	0.295343	0.245854	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450492	TAAAATAGAGAGGAG[G/T]CTTGTGGAAGAGGAA	10612
rs34252093	in-del	-/T			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475697	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCCCGC	10612
rs34253484	snp	A/G	0.440927	0.161391	intron-variant	TRIM3	GRCh38.p7	11:6452943	GACTAATGACCAAGT[A/G]CCACCCTCCGCCCTA	10612
rs34438642	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6468082	TGAGCTCAGGAGTTC[A/G]AGATCAGTCTGGGCA	10612
rs34910224	in-del	-/C			intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473494	ACCACCACCACCACC[-/C]TCGGCCGCAGCGTTC	10612
rs34965324	in-del	-/C			intron-variant	TRIM3	GRCh38.p7	11:6467185	ATGCTGTGAGAAAGA[-/C]ACACTTTTGATTGAG	10612
rs35040531	in-del	-/C			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450381	CATCACTGTATCTCC[-/C]AGCTTCTAGCATACT	10612
rs35117064	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475280	CAACCTCTTATCCAC[C/T]TGAGTTCAGCACATA	10612
rs35345984	in-del	-/G			intron-variant	TRIM3	GRCh38.p7	11:6468946	GCTGTGCCTTATGTT[-/G]TGTGTAAGGGTGGGC	10612
rs35484484	in-del	-/T			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475680	CTTCAGGTCTCAGCT[-/T]TTTTTTTTTTTTTTT	10612
rs35562657	in-del	-/C			intron-variant	TRIM3	GRCh38.p7	11:6450789	GGAAGTGGGATCTCC[-/C]AGAGCCAAGATATAG	10612
rs35587539	in-del	-/T			intron-variant	TRIM3	GRCh38.p7	11:6456009	TACATTCTATCTTTT[-/T]CAGTAGCCTGTAGCT	10612
rs35638708	in-del	-/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449789	AACACAACTCTTGAT[-/T]CCATCTCAAATCCCT	10612
rs35717222	snp	A/G	0.284471	0.247612	intron-variant	TRIM3	GRCh38.p7	11:6462533	CCACCTCAGCCTCCC[A/G]ATTAGCTAGAACTAC	10612
rs41275188	snp	A/C	0.000694839	0.0186262	intron-variant	TRIM3	GRCh38.p7	11:6457257	GCAATAACACCATCA[A/C]AATGGACGATGGTAG	10612
rs41275190	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6457531	GCTTTGCCGAACTTT[C/T]CCTTCTCCCTGGGGA	10612
rs41275192	snp	C/T	0.0409577	0.137118	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458257	GCATACTGGACAGGA[C/T]AGCGTCAGGCTCTGG	10612
rs55664515	snp	C/T	0.287346	0.247195	intron-variant	TRIM3	GRCh38.p7	11:6464941	GCAGTGAGCCGAGAT[C/T]GTGCCACTACACTCC	10612
rs55996316	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6453385	TTGCTTCCTTAATAT[C/G]TCTAGAATCTGCTGG	10612
rs56024253	snp	C/G	0.114036	0.209795	intron-variant	TRIM3	GRCh38.p7	11:6468489	GCCTGGCACAAGAGA[C/G]GGGAGCCAGCAAAGG	10612
rs56046525	snp	C/G/T	0.00266112	0.0363806	intron-variant	TRIM3	GRCh38.p7	11:6457680	CCACCAGCCCAGGAC[C/G/T]CTGCCCAGTGCCTAC	10612
rs56146361	snp	C/T	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6474034	CCCCGCCCGCCGCCG[C/T]GGAGGCCCCGCCCAC	10612
rs56202623	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6453251	AGCTATCTCAAACAT[C/G]TGCAAAAGTGAATTC	10612
rs56716552	snp	C/T	0.319856	0.240042	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448323	TGGCTGTGTGCTGGG[C/T]AGAGGTCATTCCCTC	10612
rs56752241	snp	C/T	0.00279162	0.0372561	intron-variant	TRIM3	GRCh38.p7	11:6461972	TCTCTCCAATTTCAC[C/T]TCATCCCACTTTACT	10612
rs58121083	snp	A/G	0.00795532	0.062565	intron-variant	TRIM3	GRCh38.p7	11:6468742	CATGGCAGGGATTTG[A/G]TCATGAAGGGTGGCA	10612
rs58262951	in-del	-/AT	0.428182	0.17536	intron-variant	TRIM3	GRCh38.p7	11:6455268	TTCCTAATTTTACAC[-/AT]GAGTTAACTGAAGCT	10612
rs58804533	snp	A/G	0.285257	0.247501	intron-variant	TRIM3	GRCh38.p7	11:6471717	CAAATTGCTACAGCA[A/G]CAAACTGGAGGAAGT	10612
rs59935341	snp	C/T	0.0607341	0.163335	intron-variant	TRIM3	GRCh38.p7	11:6472590	TTCTCTCGGCAAGAA[C/T]GCCATTGTCTCCTAA	10612
rs60487402	snp	A/C/G	0.039204	0.134763	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475301	TCAGCACATAGCACA[A/C/G]GATGCTCCAGTGCTT	10612
rs60616451	snp	C/T	0.287346	0.247195	intron-variant	TRIM3	GRCh38.p7	11:6471923	AAAAGGCAGAGGTTA[C/T]ACATGATGCTTTTAC	10612
rs60959926	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6459906	CTGTAACAATAAACA[C/T]CCAGGTTGAGGTCAC	10612
rs61148475	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6467797	GATTTTATCCTAAGT[C/T]GGAGGGGGGGATGAT	10612
rs61613299	snp	C/T	0.209084	0.246629	intron-variant	TRIM3	GRCh38.p7	11:6455231	TCATTTAACACTCCC[C/T]GCAACCCTATCAGAT	10612
rs61758091	snp	C/T	1.65999e-05	0.00288091	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457460	CTAAGGCAATTGCTG[C/T]GGACAGCTGTGGCAA	10612
rs61876782	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6455436	ACTACAAGAAACAGA[A/G]GGAAAAAAAGGCACA	10612
rs61876783	snp	A/G/T	4.94222e-05	0.00497078	missense, synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456147	ACCTTGTAAATTGGT[A/G/T]AATTCACCTTTCTCC	10612
rs61876784	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6457072	GAGCAGACTGGCACA[G/T]GGGGAGTCTCTGTGA	10612
rs61876785	snp	C/G	0.150667	0.229419	intron-variant	TRIM3	GRCh38.p7	11:6459524	TTACGTTTCTGTTAG[C/G]AGGAGAAAGGGCAAG	10612

Full records

It may take some time, please wait.