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
rs870371	snp	C/T	0.188631	0.242351	intron-variant	TRIM9	GRCh38.p7	14:51022724	AGGAGAGGATGCCCA[C/T]AGCCTTGGGTAGCCA	114088
rs873913	snp	A/G	0.318656	0.240388	intron-variant	TRIM9	GRCh38.p7	14:51004874	ACGTCTAATTCCCAA[A/G]GTTTCTTTCTGTTTC	114088
rs873914	snp	G/T	0.499995	0.00159744	intron-variant	TRIM9	GRCh38.p7	14:51005127	ATAACCCTGAACGCA[G/T]GTTTTGAGTCCATGC	114088
rs873915	snp	A/C	0.44768	0.153045	intron-variant	TRIM9	GRCh38.p7	14:51005906	CTCTCTTATTAGCTA[A/C]GGATTTAACTGACCC	114088
rs875204	snp	A/G	0.29278	0.246313	intron-variant	TRIM9	GRCh38.p7	14:51027510	TGACTGGAGGGATTC[A/G]CAGGACAGATTCCTG	114088
rs875205	snp	A/T	0.471292	0.116318	intron-variant	TRIM9	GRCh38.p7	14:51027781	GAGCAGGCAATAATA[A/T]GAGAGGCATATTTTA	114088
rs875206	snp	A/C	0.36021	0.224397	intron-variant	TRIM9	GRCh38.p7	14:51027936	ACACTTAGATGTTTC[A/C]GTACAGAAGTAAAAT	114088
rs875207	snp	A/G	0.471004	0.116864	intron-variant	TRIM9	GRCh38.p7	14:51027950	CAGTACAGAAGTAAA[A/G]TTGATTTGGTTACAC	114088
rs882413	snp	C/T	0.3742	0.216966	intron-variant	TRIM9	GRCh38.p7	14:51028680	AATATCCAAGAAATC[C/T]GAATGTCACTGCTTA	114088
rs882414	snp	C/T	0.473174	0.112665	intron-variant	TRIM9	GRCh38.p7	14:51028413	GCTTATAAATGTGAT[C/T]AAAATACCAACCTAT	114088
rs882415	snp	A/T	0.473174	0.112665	intron-variant	TRIM9	GRCh38.p7	14:51028403	GTGATTAAAATACCA[A/T]CCTATAAAAACAATG	114088
rs883690	snp	A/G	0.380138	0.213458	utr-variant-3-prime, nc-transcript-variant	TRIM9	GRCh38.p7	14:50976642	CCAGGGTTCTGGCCT[A/G]TCCTAATTATAGAGC	114088
rs883897	snp	C/T	0.191461	0.24305	intron-variant	TRIM9	GRCh38.p7	14:51020890	TCACCATGTGACTGT[C/T]GCAAACTGTTCACCA	114088
rs885251	snp	C/G	0.494855	0.0504572	intron-variant	TRIM9	GRCh38.p7	14:50990995	GGTATTTTAAGCTTT[C/G]TTAAGTGTGGCATTA	114088
rs946621	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM9	GRCh38.p7	14:51027580	TGCCTCTTGGAGCCT[A/G]AATACATAGAGCAAA	114088
rs946623	snp	A/G	0.191461	0.24305	intron-variant	TRIM9	GRCh38.p7	14:51020636	TGGCTTTCACGCATC[A/G]CTGGGATGCCACATC	114088
rs1016302	snp	C/T	0	0	downstream-variant-500B	TRIM9	GRCh38.p7	14:50975228	AGTTTTTATCTATTG[C/T]GGATGACAATTCACC	114088
rs1049371	snp	C/T	0.310386	0.242597	utr-variant-3-prime, nc-transcript-variant	TRIM9	GRCh38.p7	14:50975952	CATTCACAGCCTAAT[C/T]TTCTGGAGTAGTCCA	114088
rs1538616	snp	A/G	0.111928	0.208413	intron-variant	TRIM9	GRCh38.p7	14:50988754	GAGAATTGCTTGTTT[A/G]GTTAAGCTGGGATCA	114088
rs1556926	snp	A/G	0.467132	0.12391	intron-variant	TRIM9	GRCh38.p7	14:51029303	AGCCATCAAGCTGCC[A/G]GTGCTTGTTTGCCGC	114088
rs1556927	snp	G/T	0.498547	0.0269177	intron-variant	TRIM9	GRCh38.p7	14:51029178	TTGTCCCAGTTTATC[G/T]CTATCCAATATTTGT	114088
rs1556928	snp	A/G	0.372794	0.217765	intron-variant	TRIM9	GRCh38.p7	14:51029082	CTTCTGCCTGGGCAC[A/G]CTCAGCAGCTTGGGC	114088
rs1556929	snp	C/G	0.325563	0.238307	intron-variant	TRIM9	GRCh38.p7	14:51028980	CGTCCTCCACAGTCA[C/G]TCCCAGGGTAAGTGC	114088
rs1953874	snp	C/G	0.271432	0.24908	intron-variant	TRIM9	GRCh38.p7	14:51019223	CAGTATTCCAACAGT[C/G]AGCAGAGCACACTGG	114088
rs1953880	snp	C/T	0.464203	0.128908	intron-variant	TRIM9	GRCh38.p7	14:51013346	CCAGAAATAAACTCT[C/T]ACATACTTGCTCAAA	114088
rs1953881	snp	C/T	0.464203	0.128908	intron-variant	TRIM9	GRCh38.p7	14:51013162	gatcaaagaactaaa[C/T]acaaaacctaaaact	114088
rs1953882	snp	A/G	0.464309	0.12873	intron-variant	TRIM9	GRCh38.p7	14:51012971	ccaacagtatgaaat[A/G]tttgaaaatcatata	114088
rs1953883	snp	C/G	0.283684	0.24772	intron-variant	TRIM9	GRCh38.p7	14:51012853	tgattagcagcgagg[C/G]tacacaaacagccga	114088
rs1953887	snp	C/G	0.282895	0.247826	intron-variant	TRIM9	GRCh38.p7	14:51008398	TCTTTTTAACTGTTT[C/G]TTTTGAAATACACAA	114088
rs1953888	snp	C/T	0.040671	0.13668	intron-variant	TRIM9	GRCh38.p7	14:51008281	AAACCAGGAAGTTGA[C/T]ACTTAACAGTGTGTG	114088
rs1953889	snp	A/T	0.197703	0.244469	intron-variant	TRIM9	GRCh38.p7	14:51007954	TGTATGCTTTTATCA[A/T]AGAGAGATTATATAA	114088
rs1953890	snp	A/G	0.198634	0.244666	intron-variant	TRIM9	GRCh38.p7	14:51007746	TTTTTGAAATAGTGT[A/G]TAGATTGGAAATAAG	114088
rs1953891	snp	A/G	0.225893	0.248835	intron-variant	TRIM9	GRCh38.p7	14:51023169	TTTTGATAAATTTAA[A/G]TGATAAATATTTATC	114088
rs1953892	snp	A/G	0.492823	0.0594727	intron-variant	TRIM9	GRCh38.p7	14:51020286	GATACAGGCCTCCAC[A/G]GCTCGCTCGCTCTCC	114088
rs1953893	snp	A/G	0.313082	0.241911	intron-variant	TRIM9	GRCh38.p7	14:51019970	TGAGTGTGTACTTAC[A/G]CAGTCTTTATAATCT	114088
rs1959529	snp	C/G	0.493748	0.0555599	intron-variant	TRIM9	GRCh38.p7	14:51016754	CTTTGGCACCAGGGA[C/G]CAGTTTCATGGAAGA	114088
rs1959532	snp	A/G/T	0.00279162	0.0372561	intron-variant	TRIM9	GRCh38.p7	14:51003576	GTTTTAATTACACAT[A/G/T]ACATCATGTATTTCA	114088
rs1959533	snp	A/T	0.404559	0.196498	intron-variant	TRIM9	GRCh38.p7	14:50985194	AAGGCTGATTTCAGC[A/T]AAGCTAGACTTGTGT	114088
rs1959534	snp	C/T	0.498392	0.028309	intron-variant	TRIM9	GRCh38.p7	14:50984831	AATGTACTGAAATAT[C/T]GTTACAGTCTTTGTA	114088
rs1959535	snp	A/G	0.103082	0.202275	intron-variant	TRIM9	GRCh38.p7	14:50980071	TCCAATTTCTCATGC[A/G]TGTGGTTTAGGTGCA	114088
rs1959536	snp	A/C	0.215747	0.247642	intron-variant	TRIM9	GRCh38.p7	14:50980053	TGGTTTAGGTGCAAC[A/C]AAAGTGCTTCTTATT	114088
rs2039795	snp	C/T	0.289165	0.246913	intron-variant	TRIM9	GRCh38.p7	14:51011035	TGGCCTTCCAGGTCC[C/T]CCACCATCCACGCAA	114088
rs2105230	snp	C/T	0.233818	0.249476	intron-variant	TRIM9	GRCh38.p7	14:51005990	AAGAAAGTAGGTTTG[C/T]AGTTGGCTTTTACGT	114088
rs2275460	snp	A/G	0.252421	0.249988	intron-variant	TRIM9	GRCh38.p7	14:50987416	GAAAAGCTAACTTTA[A/G]TATTGTAAGTTCAGA	114088
rs2275461	snp	A/G	0.0310518	0.120672	intron-variant	TRIM9	GRCh38.p7	14:50987380	ACTCTTGGAGGTATT[A/G]AATTAAAACTTGCCA	114088
rs2275462	snp	A/C	0.476929	0.104895	missense, nc-transcript-variant	TRIM9	GRCh38.p7	14:50979498	GGTCCTCCTCGACTT[A/C]AATAGAAAAAACTTG	114088
rs2275463	snp	C/G	0.134494	0.221717	intron-variant, utr-variant-3-prime	TRIM9	GRCh38.p7	14:50979251	TGAAGGAGAGGAGGA[C/G]AGAAAGGGATCAGCA	114088
rs2297889	snp	A/T	0.40118	0.19911	intron-variant	TRIM9	GRCh38.p7	14:51009076	TGCAAGTGAAAGGTA[A/T]GTCCTTGCATCCCCC	114088
rs2356732	snp	C/T	0.313082	0.241911	intron-variant	TRIM9	GRCh38.p7	14:51027106	GCACAGTGCATGATG[C/T]GTGCTTAATAAATGC	114088
rs2356733	snp	A/G	0.450859	0.148847	intron-variant	TRIM9	GRCh38.p7	14:51027243	CTGCCTCCCAGGTTC[A/G]AGCGATTCTCCTGCC	114088
rs2884018	snp	A/C	0.450734	0.149016	intron-variant	TRIM9	GRCh38.p7	14:51027261	CGATTCTCCTGCCTC[A/C]GCCTCCCGAATAGCT	114088
rs2999394	snp	A/G	0.490836	0.0670685	intron-variant	TRIM9	GRCh38.p7	14:51093311	TAACTACTGAAAGAG[A/G]AAAGGGCTTGAATTC	114088
rs3007082	snp	C/T	0.233527	0.249457	intron-variant	TRIM9	GRCh38.p7	14:51089863	TTGACTGGTGAGACA[C/T]TGACTCTGTTTGACA	114088
rs3007083	snp	G/T	0.271702	0.249056	intron-variant	TRIM9	GRCh38.p7	14:51091822	TTTTAACATTCTTTT[G/T]TGGCAGGTAGATATC	114088
rs3007084	snp	C/T			intron-variant	TRIM9	GRCh38.p7	14:51093755	GAGCGTGCCTAGCGG[C/T]CCTGGGCACTGGCGC	114088
rs3029459	in-del	-/CCAA			intron-variant	TRIM9	GRCh38.p7	14:51005555	GAAATCTATTCTCAA[-/CCAA]ACAGTAAAGCCCTTG	114088
rs3029461	in-del	-/A	0.399253	0.200558	intron-variant	TRIM9	GRCh38.p7	14:51007801	AACACATATTAAACC[-/A]AAAAAAAAAAAAAAA	114088
rs3742326	snp	C/T	0.0592355	0.161582	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TRIM9	GRCh38.p7	14:50976987	TAACTTAATTTTTTA[C/T]GTAGGTGAGTTATAT	114088
rs3813398	snp	C/G	0.485324	0.0843964	intron-variant, utr-variant-3-prime	TRIM9	GRCh38.p7	14:50997105	ATCCCGGTGAGGTGG[C/G]GGGGTGATTTCTTTG	114088
rs3829761	snp	A/G	0.386694	0.20932	utr-variant-5-prime, nc-transcript-variant	TRIM9	GRCh38.p7	14:51095209	GCCCATTGGGCGGGG[A/G]GCAAGAGATCGAAGC	114088
rs3900632	snp	G/T	0.140242	0.224618	intron-variant	TRIM9	GRCh38.p7	14:51023632	AAATCAAATAAAAAG[G/T]TTATATCCAGCATTT	114088
rs4077264	snp	A/G	0.240765	0.249829	intron-variant	TRIM9	GRCh38.p7	14:51063859	tttttagtgtcaagc[A/G]gattgaaacaagatt	114088
rs4077265	snp	A/T	0.445592	0.155704	intron-variant	TRIM9	GRCh38.p7	14:51064135	ctgatatttgatgtg[A/T]atgttagctgtaggc	114088
rs4077266	snp	G/T	0.322245	0.239334	intron-variant	TRIM9	GRCh38.p7	14:51064679	TCTATAGGATTTTTT[G/T]TGTGTGTGATATCCT	114088
rs4131106	snp	G/T			intron-variant	TRIM9	GRCh38.p7	14:51072051	TTCCTTCCTTCCCGG[G/T]GTTCTCTGGGCTGCC	114088
rs4243567	snp	C/T	0.377977	0.21476	intron-variant	TRIM9	GRCh38.p7	14:51033241	GGGACTACAGGTGTG[C/T]GCCACCACACCTGGC	114088
rs4243568	snp	C/T	0.485799	0.0830599	intron-variant	TRIM9	GRCh38.p7	14:51056436	CAAAATAAGCAAATT[C/T]ATCATGAAATAATCC	114088
rs4243569	snp	A/G	0.482831	0.0910472	intron-variant	TRIM9	GRCh38.p7	14:51069428	TATCTAGAGGCCAGG[A/G]ATACAGTTCAACATC	114088
rs4268677	snp	A/T	0.498253	0.0295011	intron-variant	TRIM9	GRCh38.p7	14:51077616	CCAGGCTTGTCTCAA[A/T]CTCCTGTCCTCAGGT	114088
rs4337215	snp	C/G	0.145642	0.227177	intron-variant	TRIM9	GRCh38.p7	14:51077185	TCCTTTGCAGTTGGC[C/G]AACAAGCACTGATTT	114088
rs4343172	snp	C/T	0.39979	0.200158	intron-variant	TRIM9	GRCh38.p7	14:51083489	TTCTCAAACTCCTTC[C/T]GCCTCAGCCTCCCAA	114088
rs4354845	snp	A/G	0.0566069	0.158427	intron-variant	TRIM9	GRCh38.p7	14:51074334	TAAATAATGGTATGT[A/G]AAAATCTAACAATCA	114088
rs4357855	snp	G/T	0.0150606	0.0854603	intron-variant	TRIM9	GRCh38.p7	14:51036266	TATGTATTTACACCA[G/T]AGAAATTGGCAAACA	114088
rs4375571	snp	C/T	0.433963	0.169285	intron-variant	TRIM9	GRCh38.p7	14:51048220	GGAAAATTCAGTGCA[C/T]GGGCAATCTCTGCCT	114088
rs4389065	snp	A/G	0.493386	0.0571263	intron-variant	TRIM9	GRCh38.p7	14:51074890	ATGAAAGATGCCGCA[A/G]CTACATGGTTCATCT	114088
rs4400967	snp	A/G	0.326035	0.238157	intron-variant	TRIM9	GRCh38.p7	14:51081822	atggcagagacgcat[A/G]gagtaaggtactagg	114088
rs4418980	snp	C/G	0.0577344	0.159793	intron-variant	TRIM9	GRCh38.p7	14:51035623	AGAACGCTATACCAC[C/G]CGGAAGAACATGGTG	114088
rs4426259	snp	C/G	0.397633	0.201754	intron-variant	TRIM9	GRCh38.p7	14:51083575	AATACTTTGCAGCAG[C/G]ATTCTTCACACGTCT	114088
rs4444245	snp	A/C	0.49089	0.0668743	intron-variant	TRIM9	GRCh38.p7	14:51084351	AAGTAAAAAGTAGAG[A/C]AAATTCTATTTAATA	114088
rs4447338	snp	C/T	0.398174	0.201356	intron-variant	TRIM9	GRCh38.p7	14:51083358	CTGGGCTCAAGTGAC[C/T]CTCCTGCCTCAGGAG	114088
rs4450305	snp	C/T	0.397633	0.201754	intron-variant	TRIM9	GRCh38.p7	14:51083529	ATTACAGGTGTGAGG[C/T]ACCATGCCCAGCAGA	114088
rs4479142	snp	C/T	0.432742	0.184336	intron-variant	TRIM9	GRCh38.p7	14:51064179	TTAGAACATAGACTG[C/T]GTATATTGACTATGA	114088
rs4480710	snp	C/G	0.398534	0.201091	intron-variant	TRIM9	GRCh38.p7	14:51059365	AAATGCAGGCCATCC[C/G]TTAAAATATACAGAT	114088
rs4496046	snp	C/T	0.397994	0.201489	intron-variant	TRIM9	GRCh38.p7	14:51083406	ACTACAGGCATGCGC[C/T]ACCATGCCCAGCTAA	114088
rs4505215	snp	A/G	0.286825	0.247273	intron-variant	TRIM9	GRCh38.p7	14:51074728	CGCCCAGGATAAGGG[A/G]GCAGAGCTCAAAGCT	114088
rs4516123	snp	A/G	0.325091	0.238456	intron-variant	TRIM9	GRCh38.p7	14:51066273	cttcaaccaattccc[A/G]tcagacttttcatcc	114088
rs4516135	snp	A/G	0.482083	0.0929373	intron-variant	TRIM9	GRCh38.p7	14:51035352	GTGGAAACTTGAGGG[A/G]TGAATAAGAAGTCTA	114088
rs4526941	snp	A/G	0.485799	0.0830599	intron-variant	TRIM9	GRCh38.p7	14:51056117	TGTACAAAAGCAAAC[A/G]TCTACAATGGTACAA	114088
rs4530045	snp	A/G	0.386504	0.209444	intron-variant	TRIM9	GRCh38.p7	14:51057500	CCTATCTTTTATATT[A/G]TATCTGCTAAAATAA	114088
rs4539521	snp	A/G	0.497329	0.0364438	intron-variant	TRIM9	GRCh38.p7	14:51041240	ATGAAAATAAATCTC[A/G]CCATGGGAATTAGTT	114088
rs4551942	snp	A/T	0.499999	0.000599041	intron-variant	TRIM9	GRCh38.p7	14:51026944	AACAATTCTGAATTC[A/T]GAAATGCTGCCAGTT	114088
rs4606614	snp	C/T	0.17654	0.238964	intron-variant	TRIM9	GRCh38.p7	14:51063252	ATATACTGGAGTAGG[C/T]GGAATAAAAAATTCG	114088
rs4609754	snp	C/T	0.177503	0.239258	intron-variant	TRIM9	GRCh38.p7	14:51052207	AATTATCTCAATATA[C/T]ATTTTTCCAAAATCA	114088
rs4609755	snp	C/G	0.446249	0.154875	utr-variant-5-prime, nc-transcript-variant	TRIM9	GRCh38.p7	14:51095476	GCAGCGAGTGGGCTG[C/G]CGGAGGGGGCTGGGG	114088
rs4616215	snp	C/T	0.0248432	0.108648	intron-variant	TRIM9	GRCh38.p7	14:51053426	AGTTCATTCAGTACT[C/T]AGTTTGTATCAGTTT	114088
rs4617764	snp	C/T	0.485866	0.0828688	intron-variant	TRIM9	GRCh38.p7	14:51056237	CCAGAAATTGGTCTA[C/T]AATCAGCAATTCTTT	114088
rs4624086	snp	C/T	0.00914312	0.0669923	intron-variant	TRIM9	GRCh38.p7	14:51070169	aaatgctgtctagca[C/T]tcctaagcacaagaa	114088
rs4898678	snp	A/C	0.0919752	0.193722	intron-variant	TRIM9	GRCh38.p7	14:50999308	TGAAAATGACACAGG[A/C]ACTGAAAAGGCAAAG	114088
rs4898679	snp	C/T	0.0103295	0.0711199	intron-variant	TRIM9	GRCh38.p7	14:51036123	CTTTTTGCCATGCCC[C/T]GAGGCAAAAAGTGGC	114088
rs4898680	snp	A/C	0.499994	0.00179711	intron-variant	TRIM9	GRCh38.p7	14:51060082	ATAAATCACCTCCTG[A/C]CTGGAATACTTCAGA	114088

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