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
rs2879	snp	A/T	0	0	utr-variant-3-prime	TRIM33	GRCh38.p7	1:114392931	AGCTAATGTATTAAA[A/T]AACCATGAAAAGAAA	51592
rs1113207	snp	C/T	0.416382	0.186593	intron-variant	TRIM33	GRCh38.p7	1:114490890	CAGCACAGATGAAGG[C/T]GAAGGTCAGCCACAT	51592
rs1125002	snp	A/G	0.0209421	0.100162	utr-variant-3-prime	TRIM33	GRCh38.p7	1:114395553	TTTTTGGAAAGTGAG[A/G]AATAGCAGCAGTATA	51592
rs1146149	snp	A/C	0.00676609	0.0577691	intron-variant	TRIM33	GRCh38.p7	1:114457356	gacatcttctggtcc[A/C]aaaatcctagtggtt	51592
rs1230794	snp	C/T	0.00716266	0.059414	intron-variant	TRIM33	GRCh38.p7	1:114409768	aataccttcacagta[C/T]catctatactgatgt	51592
rs1230795	snp	C/T	0	0	intron-variant	TRIM33	GRCh38.p7	1:114405313	CTTCTAACCAGTGCA[C/T]AGTATTTCTATAAAA	51592
rs2092510	snp	C/G	0.00716266	0.059414	intron-variant	TRIM33	GRCh38.p7	1:114448938	tctagtctttgtgtt[C/G]tttgacctcctttcc	51592
rs2143583	snp	A/C	0.368938	0.219895	intron-variant	TRIM33	GRCh38.p7	1:114446589	TTCCATTTTACATCT[A/C]CTGTTGGCTTTTTAA	51592
rs2179657	snp	C/G/T	0.0159017	0.0877405	synonymous-codon	TRIM33	GRCh38.p7	1:114402772	GCAGGGGTTAAGCCC[C/G/T]GTGGACCAAAGGGTA	51592
rs2336578	snp	A/C	0.00597247	0.0543191	intron-variant	TRIM33	GRCh38.p7	1:114503951	tgcttctgctgcgga[A/C]gaaagtggaagaaga	51592
rs2336579	snp	A/G	0.00517822	0.0506191	intron-variant	TRIM33	GRCh38.p7	1:114470764	actaggctaactggc[A/G]caagaggcctagcat	51592
rs2336580	snp	A/G	0.194278	0.243711	intron-variant	TRIM33	GRCh38.p7	1:114460781	GTTTTATAGAGAGAG[A/G]GGGACTGAGGAAAGC	51592
rs2336581	snp	A/C	0.00980368	0.0693234	intron-variant	TRIM33	GRCh38.p7	1:114460618	ATTAAAGACATCAGC[A/C]CCGTAGGAGAGGTTT	51592
rs2336582	snp	A/C	0	0	intron-variant	TRIM33	GRCh38.p7	1:114460602	CCGTAGGAGAGGTTT[A/C]CCaaaaaaaaaaaaa	51592
rs2878746	snp	A/G	0.0788843	0.182262	intron-variant	TRIM33	GRCh38.p7	1:114461066	gagccactgagcttg[A/G]cCCCGGCCTCTGGTA	51592
rs2878747	snp	A/C	0	0	intron-variant	TRIM33	GRCh38.p7	1:114460695	ctggagaagggcaga[A/C]caatagagaaataat	51592
rs3077592	in-del	-/GT			intron-variant	TRIM33	GRCh38.p7	1:114414069	CACGAATTTAAAAAC[-/GT]GTGTGTGTGTGTGTG	51592
rs3789615	snp	C/T	0.480064	0.0978296	intron-variant	TRIM33	GRCh38.p7	1:114398704	GGCACCCAAATTACA[C/T]CAGCAATAAAGAGAC	51592
rs3789616	snp	A/C	0.0869089	0.189476	intron-variant	TRIM33	GRCh38.p7	1:114398911	CTCAAAAAAAAAAAA[A/C]AAAACAAAACAAAAC	51592
rs3789617	snp	A/C	0.475613	0.107697	intron-variant	TRIM33	GRCh38.p7	1:114398931	CAAAACAAAACAAAA[A/C]AAAAAACAAAAAACT	51592
rs3789618	snp	C/T	0.0174175	0.0916809	intron-variant	TRIM33	GRCh38.p7	1:114411773	ATAACCTCCAACAGA[C/T]AGGTGCTAACTGAAG	51592
rs3789619	snp	A/C	0.329783	0.236927	intron-variant	TRIM33	GRCh38.p7	1:114416324	CATAAGTGAAACACT[A/C]AATATACTACAAAAC	51592
rs3789620	snp	C/T	0.0119091	0.0762411	intron-variant	TRIM33	GRCh38.p7	1:114420198	GATACTTTTCTTCGG[C/T]TGAAAGGGGCAAAAG	51592
rs3789621	snp	C/T			intron-variant	TRIM33	GRCh38.p7	1:114428276	CAAAAAAATTTTGTG[C/T]CACCAGTGCCACCTC	51592
rs3789622	snp	C/T	0	0	intron-variant	TRIM33	GRCh38.p7	1:114444145	CAGAGGCAAAAATCA[C/T]GGTGTGGGCTCATGA	51592
rs3827735	snp	A/C	0.422787	0.180679	intron-variant	TRIM33	GRCh38.p7	1:114510087	CATTTAATCCATAGT[A/C]CTCCTCTCTCCTATC	51592
rs4839009	snp	C/T	0.00716266	0.059414	intron-variant	TRIM33	GRCh38.p7	1:114428170	GTTAAAAATAGTGTC[C/T]TCCTATTAGATTAAT	51592
rs4839379	snp	G/T	0.00676609	0.0577691	intron-variant	TRIM33	GRCh38.p7	1:114499473	GGGGTAAGGAAAAAA[G/T]TTTTCTCCTGAGAAT	51592
rs5777192	in-del	-/A	0.5	0	intron-variant	TRIM33	GRCh38.p7	1:114398011	AAGGATACCAGAGTC[-/A]AAAAAAAAAAAGGGA	51592
rs6537825	snp	A/G	0.192464	0.243289	missense	TRIM33	GRCh38.p7	1:114405659	ATATCTGCAGGTTCA[A/G]TTTTCACATGGTTTT	51592
rs6537826	snp	C/T	0.416545	0.186448	intron-variant	TRIM33	GRCh38.p7	1:114414632	TAGGTTGATGCCTTA[C/T]AATTTCCCCTTTGAG	51592
rs6537827	snp	C/T	0.416708	0.186302	intron-variant	TRIM33	GRCh38.p7	1:114423190	gatataacgataatt[C/T]GGTCCACAGAAAAAG	51592
rs6537828	snp	C/G	0.414905	0.187899	intron-variant	TRIM33	GRCh38.p7	1:114445096	agggtatgtgaccat[C/G]aacacacatcaataa	51592
rs6537829	snp	A/T	0.0119091	0.0762411	intron-variant	TRIM33	GRCh38.p7	1:114467533	CTTGTTACACCAATA[A/T]TTACAAGTCAAGCAG	51592
rs6537831	snp	A/G	0.00478085	0.0486577	intron-variant	TRIM33	GRCh38.p7	1:114473046	caaatcatgaggtca[A/G]gagatagagaccatc	51592
rs6537832	snp	A/G	0.41833	0.184838	intron-variant	TRIM33	GRCh38.p7	1:114473793	AAAACAAAGAGCAAA[A/G]CAATCAacgtagatc	51592
rs6537833	snp	C/G	0.416382	0.186593	intron-variant	TRIM33	GRCh38.p7	1:114492087	agcatctcccagttt[C/G]acctcagctgggaat	51592
rs6656393	snp	G/T	0.41833	0.184838	intron-variant	TRIM33	GRCh38.p7	1:114426978	ATATACAGAGTAGAC[G/T]CTCAACTTTCTTAAG	51592
rs6656726	snp	A/G	0.368733	0.220005	intron-variant	TRIM33	GRCh38.p7	1:114457438	gcattaactgagact[A/G]aatctatgactgaag	51592
rs6658339	snp	C/T	0.0205511	0.0992634	intron-variant	TRIM33	GRCh38.p7	1:114430101	TAAAATAAGGTAAAA[C/T]ACACAAATGACTCAA	51592
rs6658383	snp	A/G	0.416545	0.186448	intron-variant	TRIM33	GRCh38.p7	1:114496521	GGGATGTGGCATCAC[A/G]AGGCatagtaaataa	51592
rs6660859	snp	C/T	0.0788843	0.182262	intron-variant	TRIM33	GRCh38.p7	1:114496277	AAATGAGTTGTGTAA[C/T]TTGAATTTTAGCATT	51592
rs6660911	snp	C/G	0.0267878	0.112589	intron-variant	TRIM33	GRCh38.p7	1:114418184	caaggcagtaggaga[C/G]agagtgagtgcagag	51592
rs6660976	snp	C/T	0	0	intron-variant, upstream-variant-2KB	TRIM33	GRCh38.p7	1:114466370	gcaagaaagggttta[C/T]ttggcaggcctgggt	51592
rs6661053	snp	C/T	0.416708	0.186302	intron-variant	TRIM33	GRCh38.p7	1:114496497	ACATGTCCCATCAAA[C/T]GAAAACATGGGATGT	51592
rs6666770	snp	A/G	0.414576	0.188188	intron-variant	TRIM33	GRCh38.p7	1:114490111	aaaaaaaaaGaaaag[A/G]aaaggaaagaaaaaa	51592
rs6667058	snp	G/T	0.416382	0.186593	intron-variant	TRIM33	GRCh38.p7	1:114430251	CTTTTTTCTTTTTCT[G/T]TTTTTCATTTTGGAG	51592
rs6668327	snp	C/T	0.415563	0.18732	intron-variant	TRIM33	GRCh38.p7	1:114447634	AGCCCTAAGACTATA[C/T]GTATAGATAATGGTG	51592
rs6670743	snp	C/T	0.416218	0.186739	intron-variant	TRIM33	GRCh38.p7	1:114468862	AGCGAGTGTGCAACA[C/T]CACGAGGGAAAAGAA	51592
rs6671365	snp	C/T	0.416382	0.186593	intron-variant	TRIM33	GRCh38.p7	1:114484409	TTTGCAAGAATTATA[C/T]TGGTCATCCTTTTCA	51592
rs6671587	snp	A/G	0.418169	0.184985	intron-variant	TRIM33	GRCh38.p7	1:114442045	GGAACCAAATACTCA[A/G]TATCAGTCTCATACA	51592
rs6672519	snp	C/T	0.387074	0.209071	intron-variant	TRIM33	GRCh38.p7	1:114408598	gtataaaggggttca[C/T]tgtaatattctactt	51592
rs6673841	snp	A/T			intron-variant	TRIM33	GRCh38.p7	1:114475689	tccatctcaaaataa[A/T]aataaaTGTTTAACA	51592
rs6675600	snp	C/T	0.416382	0.186593	intron-variant	TRIM33	GRCh38.p7	1:114450138	ggctcacgcctgtaa[C/T]cccagctacttggga	51592
rs6677898	snp	C/T	0.0832709	0.186283	intron-variant	TRIM33	GRCh38.p7	1:114406016	TAAACTGTTAAGCTA[C/T]TGATTGGGAAGTGAG	51592
rs6682018	snp	C/T	0.0663309	0.169604	intron-variant	TRIM33	GRCh38.p7	1:114427468	TACTTGAATTTCTGC[C/T]ATTTTGGGTAATAAA	51592
rs6685174	snp	A/T	0	0	intron-variant	TRIM33	GRCh38.p7	1:114449477	aaaatacagataaaa[A/T]atgtaacaatattag	51592
rs6688160	snp	A/G	0.0209421	0.100162	intron-variant	TRIM33	GRCh38.p7	1:114452289	acatggtgaaacccc[A/G]tctctactaaaaata	51592
rs6688348	snp	A/T	0.0980852	0.198549	intron-variant	TRIM33	GRCh38.p7	1:114450273	tcaaaaaaagagaaT[A/T]CTAGATTGAAAACCT	51592
rs6690560	snp	C/G	0.416218	0.186739	intron-variant	TRIM33	GRCh38.p7	1:114434781	AAGAGATATAATTCA[C/G]GTATATATAATTTAC	51592
rs6691089	snp	A/T	0.5	0	intron-variant	TRIM33	GRCh38.p7	1:114426523	ttttttttttttttt[A/T]aaaaaaaagggcaac	51592
rs6691166	snp	A/G	0.118698	0.212744	missense	TRIM33	GRCh38.p7	1:114510877	GAGGAGGCCGCGGCC[A/G]CCCCCCCGTCGTCGG	51592
rs6692002	snp	C/T	0.416382	0.186593	intron-variant	TRIM33	GRCh38.p7	1:114430211	ACTACTTTGCCTTTA[C/T]GTACATCACATTTTA	51592
rs6693073	snp	C/T	0.0955749	0.196603	intron-variant	TRIM33	GRCh38.p7	1:114486113	aacccccatctctac[C/T]aaaaatacaaaaact	51592
rs6694561	snp	C/T	0.0410537	0.137264	intron-variant	TRIM33	GRCh38.p7	1:114466446	gactggccctttaca[C/T]gttcctgggagatga	51592
rs6694768	snp	C/T	0.415727	0.187175	intron-variant	TRIM33	GRCh38.p7	1:114410798	AAAAAAGGGCACAGT[C/T]AACAGTACATATGAG	51592
rs6695458	snp	C/T	0	0	intron-variant	TRIM33	GRCh38.p7	1:114491434	gttcctgcaagcctc[C/T]ggtcacaaaattttc	51592
rs6696058	snp	A/G	0.0178098	0.0926698	intron-variant	TRIM33	GRCh38.p7	1:114449420	gacagatgaggggac[A/G]tctgggagtgtggca	51592
rs6696993	snp	A/G	0.416382	0.186593	intron-variant	TRIM33	GRCh38.p7	1:114487839	gaagcggagcttgca[A/G]tgagccgagattgcg	51592
rs6700078	snp	C/T	0.0209421	0.100162	intron-variant	TRIM33	GRCh38.p7	1:114503230	tcatgcctgtaatac[C/T]aacactttgggaggc	51592
rs6700446	snp	A/C	0.0832709	0.186283	intron-variant	TRIM33	GRCh38.p7	1:114428625	TTGGTTTTTCTGGAC[A/C]ATATTTTTCCTAAGG	51592
rs6703214	snp	C/G	0.084728	0.187577	intron-variant	TRIM33	GRCh38.p7	1:114473782	GAGCTATACAGAAAA[C/G]AAAGAGCAAAGCAAT	51592
rs6703485	snp	A/G	0.416382	0.186593	intron-variant	TRIM33	GRCh38.p7	1:114491647	gtctttacaaaaaat[A/G]taaaaaattagctgg	51592
rs6703862	snp	C/T	0	0	intron-variant	TRIM33	GRCh38.p7	1:114474401	agcaaggccccattt[C/T]tacaaattaaaaaaa	51592
rs7511633	snp	A/G	0.416218	0.186739	intron-variant	TRIM33	GRCh38.p7	1:114456655	GAGAGATCCCAATTT[A/G]CACTTACTCTATCAC	51592
rs7512590	snp	A/G	0.0562907	0.15804	intron-variant	TRIM33	GRCh38.p7	1:114420491	AACTAGCCTTTTAGC[A/G]AAAGTGATATTAATC	51592
rs7514446	snp	C/T	0.0930568	0.194599	intron-variant	TRIM33	GRCh38.p7	1:114419933	ATATCTTTTAAAACT[C/T]TTACATAAGCCCATT	51592
rs7515983	snp	A/G	0.0832709	0.186283	intron-variant	TRIM33	GRCh38.p7	1:114418041	tcacactgctataaa[A/G]atactacctgagact	51592
rs7516184	snp	G/T	0.0788843	0.182262	intron-variant	TRIM33	GRCh38.p7	1:114418244	ttgtgagaacagcat[G/T]agggaaaccaccgcc	51592
rs7516386	snp	C/T	0.368938	0.219895	intron-variant	TRIM33	GRCh38.p7	1:114436467	AATATTTTCAGAGAG[C/T]ttttttgtttgtttt	51592
rs7519209	snp	A/G	0.416545	0.186448	intron-variant	TRIM33	GRCh38.p7	1:114443214	TAGTGAAACCCCATC[A/G]CTACTAAAAATACAA	51592
rs7520209	snp	C/T	0.351853	0.228311	intron-variant	TRIM33	GRCh38.p7	1:114477088	AAACATTCTGTCAAT[C/T]TGTCAAAAGAATATT	51592
rs7521944	snp	A/G	0.00438332	0.0466095	intron-variant	TRIM33	GRCh38.p7	1:114473757	AACCAATGAACAACA[A/G]TAAATACATGAGCTA	51592
rs7523112	snp	C/T	0.416545	0.186448	intron-variant	TRIM33	GRCh38.p7	1:114423478	atatgctataaagta[C/T]agcttttgaaactat	51592
rs7524365	snp	C/T	0.0460142	0.144533	intron-variant	TRIM33	GRCh38.p7	1:114443622	AACTATCTTACTCTT[C/T]AATAAAAATATCTGA	51592
rs7527168	snp	A/G	0.0437281	0.141251	intron-variant	TRIM33	GRCh38.p7	1:114467178	GACTAAACTAAGGCA[A/G]TATTAAAGGAAATGT	51592
rs7528577	snp	C/G	0.418169	0.184985	intron-variant	TRIM33	GRCh38.p7	1:114484816	gttgcagtgagccca[C/G]atcgcaccactgcac	51592
rs7529160	snp	C/T	0.0448719	0.142907	intron-variant	TRIM33	GRCh38.p7	1:114485426	ATCATCACTTCTTAT[C/T]CCTTTGCCTGGTATG	51592
rs7532456	snp	A/C	0.0460142	0.144533	intron-variant	TRIM33	GRCh38.p7	1:114456389	TGGTGCCAATGAATT[A/C]TTTGTACAATAATCC	51592
rs7533214	snp	C/T	0.0209421	0.100162	intron-variant	TRIM33	GRCh38.p7	1:114481308	aCacaaaattaaaac[C/T]ataggccagatgtgg	51592
rs7535520	snp	A/G	0.415891	0.18703	intron-variant	TRIM33	GRCh38.p7	1:114504927	CTCTTCTTTCTGTTT[A/G]CTGTGAGATACAGTC	51592
rs7535529	snp	C/G	0.0832709	0.186283	intron-variant	TRIM33	GRCh38.p7	1:114504956	TCACAAAGACAACGG[C/G]GGGACAAATGAAAAA	51592
rs7536927	snp	C/T	0.0737376	0.17729	intron-variant	TRIM33	GRCh38.p7	1:114423344	taagataaaactctg[C/T]tgaagaagtagaagt	51592
rs7538458	snp	A/C	0.0209421	0.100162	intron-variant	TRIM33	GRCh38.p7	1:114479353	cacgaaatgaatcaa[A/C]ccaaacacatcacag	51592
rs7538540	snp	A/C	0.084728	0.187577	intron-variant	TRIM33	GRCh38.p7	1:114509488	AAAAAGAAAAATCCC[A/C]AAATATTCTGAAGTC	51592
rs7540369	snp	A/G	0.0652144	0.168387	intron-variant	TRIM33	GRCh38.p7	1:114441547	AGACGTGATGACAAC[A/G]TACAATTATTTCAAA	51592
rs7540802	snp	A/G	0.0689305	0.172377	intron-variant	TRIM33	GRCh38.p7	1:114401098	ctggagtgcagtggc[A/G]cgatctcggctcact	51592
rs7541954	snp	C/T	0.416382	0.186593	intron-variant	TRIM33	GRCh38.p7	1:114429264	GCAATCTTGCCTCAC[C/T]GCAACCTCCACCTCC	51592
rs7544790	snp	A/G	0.418162	0.188639	intron-variant	TRIM33	GRCh38.p7	1:114481360	gcactttgggaagcc[A/G]aggtggtggatcacg	51592
rs7544820	snp	A/G	0.0174175	0.0916809	intron-variant	TRIM33	GRCh38.p7	1:114423431	taaaataatgcaaag[A/G]tttttttaactttat	51592

Full records

It may take some time, please wait.