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
rs3660780	snp	C/T	0.408163	0.193609	intron-variant	Trim2	Mm_Celera	3:84289227	CTGGAGGGACACGGA[C/T]TTAGTTCACAGCAAT	80890
rs3675100	snp	A/G	0.408163	0.193609	intron-variant	Trim2	Mm_Celera	3:84289369	GAGGTACTTCACACC[A/G]TTGGCATTCCAGACA	80890
rs3675686	snp	C/T	0.408163	0.193609	intron-variant	Trim2	Mm_Celera	3:84289434	GCATTAAAATCTTTA[C/T]AGTAGCTGAAGAGAT	80890
rs3680022	snp	C/T	0.48	0.0979796	intron-variant	Trim2	Mm_Celera	3:84283987	TTTGTCACACTCAGT[C/T]CTGTGAAACTGCTGC	80890
rs3680611	snp	C/T	0.48	0.0979796	intron-variant	Trim2	Mm_Celera	3:84284030	CCCATCGGAACTCTC[C/T]GGAACAGAGACATTG	80890
rs3680673	snp	C/T	0.48	0.0979796	intron-variant	Trim2	Mm_Celera	3:84284064	CTGCTTCTCTCGCTC[C/T]GCCTCTAGCTCTCGG	80890
rs3681950	snp	A/C	0.5	0	intron-variant	Trim2	Mm_Celera	3:84284253	AACCAGCGGCTGAAG[A/C]TGTCTAGTCGGCAAG	80890
rs3681991	snp	A/G	0.5	0	intron-variant	Trim2	Mm_Celera	3:84284277	CGGCAAGTGAGACGG[A/G]GCAGAGTCCCCGTCC	80890
rs3682638	snp	C/T	0.5	0	intron-variant	Trim2	Mm_Celera	3:84284388	TGCATTGAGTCTTGA[C/T]TGATGTAACTGAGAG	80890
rs6170577	snp	C/T	0.495868	0.0452663	intron-variant	Trim2	Mm_Celera	3:84208491	GTGATGTGCTGACAA[C/T]GGGCCACTTTGCAGA	80890
rs6171085	snp	C/T	0.495868	0.0452663	intron-variant	Trim2	Mm_Celera	3:84208576	TAATCTGTCCTCACA[C/T]GGGCTCTATCTGCTG	80890
rs6171566	snp	A/G	0.5	0	intron-variant	Trim2	Mm_Celera	3:84208620	TGCGCTTAAGGAAAG[A/G]AAAATGCCATAGACT	80890
rs6171620	snp	C/T	0.5	0	intron-variant	Trim2	Mm_Celera	3:84208660	TCTAGAGCGCTGACA[C/T]CCACAGTGTGGTTGG	80890
rs6172685	snp	C/G/T	0.5	0	intron-variant	Trim2	GRCm38.p3	3:84208822	TTTAGCAATTGGGGG[C/G/T]GGGGAGGGATGTCAA	80890
rs6183172	snp	A/G	0.431413	0.172016	intron-variant, upstream-variant-2KB	Trim2	Mm_Celera	3:84221652	TAACCAATATTTCAG[A/G]ATCAAAGGCATACAT	80890
rs6250901	snp	A/T	0.5	0	intron-variant	Trim2	Mm_Celera	3:84256477	TACAGTGTGTTAGGC[A/T]AAATGGAAACAGTGA	80890
rs6251402	snp	C/T	0.5	0	intron-variant	Trim2	Mm_Celera	3:84192671	CCCATGGTAGAGAAC[C/T]GCTATATTCTAAGTG	80890
rs6264062	snp	A/C	0.5	0	intron-variant	Trim2	Mm_Celera	3:84192718	TTTTTTTCTTCCAAC[A/C]ACATAAACTTTGAAG	80890
rs6264132	snp	C/T	0.5	0	intron-variant	Trim2	Mm_Celera	3:84192767	AACTCTTGTAAGTTT[C/T]CAAGTTCCTTCAGGT	80890
rs6264666	snp	C/T	0.5	0	intron-variant	Trim2	Mm_Celera	3:84192887	TTAGTTTCTCTCATA[C/T]AGGACATGNCTACTA	80890
rs6264679	snp	A/G	0.5	0	intron-variant	Trim2	Mm_Celera	3:84192896	CTCATANAGGACATG[A/G]CTACTATATTCATTT	80890
rs6306184	snp	A/G	0.5	0	utr-variant-3-prime	Trim2	GRCm38.p3	3:84162181	AAATACAGTGAACAC[A/G]CACAGGTACCCAGGT	80890
rs6319349	snp	C/T	0.432133	0.171253	intron-variant	Trim2, LOC105244477	Mm_Celera	3:84239995	CTTGTTTCTGGCCGT[C/T]ACTTGCTTTTGCATT	80890
rs6319926	snp	C/T	0.48	0.0979796	intron-variant	Trim2, LOC105244477	Mm_Celera	3:84240105	AAGCAGCATTTTAGC[C/T]GGGCAGTGGTGGCAC	80890
rs6320332	snp	A/G	0.5	0	utr-variant-3-prime	Trim2	GRCm38.p3	3:84162525	TCCATCTCCAGCACC[A/G]CAAAACAAAGAACCA	80890
rs6320903	snp	A/G	0.5	0	utr-variant-3-prime	Trim2	Mm_Celera	3:84162624	cacgccattaatccc[A/G]gcacttgggagtcag	80890
rs13468633	snp	A/G	0.375	0.216506	utr-variant-3-prime	Trim2	GRCm38.p3	3:84160522	TCTGTCTTGAAACAC[A/G]GGAGAAACAAGACTC	80890
rs29974785	snp	A/G	0.5	0	intron-variant	Trim2	GRCm38.p3	3:84295153	TGTGCAGGTATGCAT[A/G]TGGCTGTGTGTGTGT	80890
rs29979513	snp	G/T	0.429688	0.173817	intron-variant	Trim2	GRCm38.p3	3:84179467	AGACAGTCCTGCATC[G/T]TGAAGGAAACTCCTG	80890
rs30005821	snp	A/C/T	0.5	0	intron-variant	Trim2	GRCm38.p3	3:84206986	CCCTGACAGCTCCAG[A/C/T]GCCATGCTTGCCTGC	80890
rs30013276	snp	A/T	0.336735	0.234472	intron-variant	Trim2	GRCm38.p3	3:84196340	AGAGCCCATCACTCT[A/T]GGGTTGCCAGCCCTC	80890
rs30013756	snp	A/C	0.444444	0.157135	intron-variant	Trim2	GRCm38.p3	3:84297960	CCTCTTCCTACTCCT[A/C]TTTTTCCTCTCTCTC	80890
rs30014459	snp	C/T	0.444444	0.157135	intron-variant	Trim2, LOC105244477	Mm_Celera	3:84237921	TGGATTCAGGATCAC[C/T]GTGGAAACACATTTT	80890
rs30014552	snp	G/T	0.5	0	intron-variant	Trim2	GRCm38.p3	3:84176707	TGCCACTGGGAGGCC[G/T]TAGGGTCCCGCGGAA	80890
rs30016168	snp	C/T	0.444444	0.157135	intron-variant	Trim2	Mm_Celera	3:84180700	CTTGGGACCAGTGAA[C/T]GTGCCTGTGAGTGGG	80890
rs30017331	snp	C/T	0.5	0	intron-variant	Trim2	GRCm38.p3	3:84301001	ATCAACCTAATTGTG[C/T]ACTGACAGATGAATG	80890
rs30028673	snp	C/G	0.5	0	intron-variant	Trim2	Mm_Celera	3:84217577	TGTGTGTGTGTGTGT[C/G]TGTCTCTCTCTCTCT	80890
rs30058368	snp	A/G	0.444444	0.157135	intron-variant	Trim2	Mm_Celera	3:84176751	CAGGGGCACAGCCCT[A/G]AAGGAGGCTGTGGGA	80890
rs30065815	snp	A/G	0.32	0.24	intron-variant	Trim2	GRCm38.p3	3:84297229	AATGAGAAGGGTAGC[A/G]AAAGAGATGGCTCCG	80890
rs30102191	snp	A/T	0.444444	0.157135	intron-variant	Trim2	Mm_Celera	3:84219837	AGGAGGAGGAGGGAG[A/T]GGAAAAAAAAAAAAC	80890
rs30105795	snp	C/T	0.444444	0.157135	intron-variant	Trim2, LOC105244477	Mm_Celera	3:84239591	ATAAAGCCACCAATA[C/T]ATACACAGAGGACCT	80890
rs30106803	snp	A/T	0.375	0.216506	intron-variant	Trim2	GRCm38.p3	3:84301524	CGGAACAGAAACAAT[A/T]CAGAGCCAAGTCAAA	80890
rs30106940	snp	C/T	0.375	0.216506	intron-variant	Trim2	Mm_Celera	3:84203598	CTTTCTTTCTTTTTT[C/T]CTTCCTTCCTTCCTT	80890
rs30107260	snp	C/T	0.48	0.0979796	intron-variant	Trim2	Mm_Celera	3:84287966	GATCTCCACAGTAAA[C/T]TTCTGGCAGTTAACT	80890
rs30107436	snp	C/T	0.444444	0.157135	intron-variant	Trim2	Mm_Celera	3:84226019	GACAGAGCACCCCAA[C/T]TGAAGACATGTTTTG	80890
rs30108568	snp	C/T	0.475309	0.108333	intron-variant, nc-transcript-variant	Trim2, LOC105244477	GRCm38.p3	3:84247040	GCTCTGGGGCAGAAA[C/T]GATGGCATGTCATGG	80890
rs30112009	snp	C/G	0.497778	0.0332592	intron-variant, upstream-variant-2KB, utr-variant-5-prime	Trim2	Mm_Celera	3:84220919	GCAGCGAGCTGCAAA[C/G]AGATTCGCGGGTGGC	80890
rs30113011	snp	A/G	0.5	0	synonymous-codon	Trim2	Mm_Celera	3:84192180	GGTGGAGTGGATGTC[A/G]TCCACAATGCTGGCC	80890
rs30113286	snp	C/T	0.5	0	intron-variant	Trim2	Mm_Celera	3:84195310	AGGAAATTTGAACCT[C/T]CCAAGGGAAGACTGA	80890
rs30114801	snp	A/G	0.484429	0.0868505	intron-variant	Trim2	GRCm38.p3	3:84197935	GGAACACAGCCTAGC[A/G]CCAAATATGTAATAG	80890
rs30116254	snp	C/G	0.391111	0.206368	intron-variant	Trim2	Mm_Celera	3:84171422	ATTTCTCCGTACAAG[C/G]AGTGCAGAGTTAACA	80890
rs30116345	snp	A/G	0.5	0	intron-variant	Trim2	GRCm38.p3	3:84294302	ACAAAAGAACCTCAC[A/G]GGCAGAGAACACGCG	80890
rs30157558	snp	C/T	0.5	0	intron-variant	Trim2	GRCm38.p3	3:84304143	AGAACTCTGAAATCC[C/T]CCCGGGATCCAGACC	80890
rs30162778	snp	A/G	0.444444	0.157135	intron-variant	Trim2	GRCm38.p3	3:84282982	GCAAAACATTCATTC[A/G]CATAAAATAAACCTG	80890
rs30167337	snp	C/T	0.486111	0.0821678	intron-variant, upstream-variant-2KB, utr-variant-5-prime	Trim2	Mm_Celera	3:84221289	AAACAATGCAGATTG[C/T]TTGAAATGTAAAATC	80890
rs30174164	snp	C/T	0.32	0.24	intron-variant	Trim2	GRCm38.p3	3:84202669	CACATGGAGCAAAAC[C/T]AGAACTATAAGCACA	80890
rs30201352	snp	C/T	0.444444	0.157135	intron-variant	Trim2	Mm_Celera	3:84296245	ACTTGTTTACACAGT[C/T]GAAAGCACACCTTTT	80890
rs30203713	snp	C/T	0.5	0	intron-variant, utr-variant-3-prime	Trim2	Mm_Celera	3:84191527	TAAGAGAAGAAAGGA[C/T]TCTACCAACAGCAAA	80890
rs30205406	snp	A/G	0.375	0.216506	intron-variant	Trim2	Mm_Celera	3:84175844	GAGCTTCCTGTACCT[A/G]TGGCCGTTATATGGA	80890
rs30208583	snp	C/T	0.375	0.216506	upstream-variant-2KB	Trim2	GRCm38.p3	3:84306906	GTCATCATGTCTTAA[C/T]ACAGCAATAGAAAAG	80890
rs30213317	snp	C/T	0.375	0.216506	intron-variant	Trim2	Mm_Celera	3:84301613	TATCTTGAATTATTT[C/T]GCCACCCAACAAAGA	80890
rs30222717	snp	G/T	0.444444	0.157135	intron-variant	Trim2	Mm_Celera	3:84283881	GCTGTCTTCTTGGGG[G/T]GCTTGACTGGGTACA	80890
rs30253491	snp	A/T	0.444444	0.157135	intron-variant	Trim2	GRCm38.p3	3:84195727	TGTAAACTTTTTTTT[A/T]AAAAAAATGTCTTCC	80890
rs30253608	snp	A/G	0.465374	0.126941	utr-variant-3-prime	Trim2	Mm_Celera	3:84164501	ACGATCTTTGATCAA[A/G]CCCAGGAAATTTGGG	80890
rs30253614	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Trim2	Mm_Celera	3:84213906	ATGAAATTTCTTAAG[C/T]CAACACTTTTAAGCT	80890
rs30253966	snp	C/T	0.387812	0.208586	intron-variant	Trim2	Mm_Celera	3:84267208	GCATTCTGAAGGCAT[C/T]TATCTGTTTCCTATC	80890
rs30256554	snp	A/G	0.375	0.216506	intron-variant	Trim2	GRCm38.p3	3:84186365	CCCCTGATTCCAATC[A/G]TCATCTAGAATTCCT	80890
rs30257661	snp	C/T	0.487535	0.077957	intron-variant	Trim2	Mm_Celera	3:84295483	TGGCTGTGGTGTGCG[C/T]CAGTGGTAGGCTGCT	80890
rs30261540	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	Trim2	Mm_Celera	3:84270814	GCCAAGGGGAGGGAG[A/G]GGCTGTGGTATCAAG	80890
rs30271449	snp	C/T	0.345679	0.230967	intron-variant, nc-transcript-variant	Trim2, LOC105244477	Mm_Celera	3:84242193	CTATGTGACAGTTTC[C/T]CCATTTAGATTCATG	80890
rs30276535	snp	C/T	0.444444	0.157135	intron-variant	Trim2	GRCm38.p3	3:84194326	TGGTAGTATCCATGA[C/T]AGTAACAGGCTCCAC	80890
rs30308351	snp	C/T	0.48	0.0979796	intron-variant	Trim2	GRCm38.p3	3:84180210	GAGAGAATGCATGCA[C/T]GCATGCACACACGCA	80890
rs30309737	snp	C/G	0.401235	0.199068	intron-variant	Trim2	Mm_Celera	3:84216793	AGCTTTGTGGCACTC[C/G]TGGGTCAGTATTAGT	80890
rs30315309	snp	A/C/T	0.444444	0.157135	intron-variant	Trim2	GRCm38.p3	3:84189666	AGGGGAGGCAGGCTG[A/C/T]GGGTAAAGACAGAAC	80890
rs30316058	snp	A/G	0.33241	0.236027	intron-variant	Trim2	Mm_Celera	3:84215956	ACTGTGACAAAGCAT[A/G]CTTGTTGTGAATGCT	80890
rs30330167	snp	A/G	0.32	0.24	intron-variant	Trim2	Mm_Celera	3:84254019	TGACCAAAGACACAC[A/G]GGGAAGCTAACAAGA	80890
rs30350924	snp	C/T	0.487535	0.077957	intron-variant	Trim2, LOC105244477	Mm_Celera	3:84237565	TGGCTGGCACAGCAT[C/T]CATGCAACTCAGCAC	80890
rs30354653	snp	A/C	0.375	0.216506	intron-variant, upstream-variant-2KB	Trim2, Gm6525	Mm_Celera	3:84172961	AGTACAGAAATATAC[A/C]TCAAAGTTCAAAGCA	80890
rs30356937	snp	C/T	0.375	0.216506	intron-variant	Trim2	Mm_Celera	3:84203595	TTTCTTTCTTTCTTT[C/T]TTCCTTCCTTCCTTC	80890
rs30357914	snp	C/T	0.46875	0.121031	intron-variant	Trim2	GRCm38.p3	3:84296619	CCTTATAACAGCCTG[C/T]GGTGATCAGGATGGC	80890
rs30367455	snp	A/C	0.495	0.0497494	intron-variant	Trim2, LOC105244477	Mm_Celera	3:84237665	GTAACGTCACCATCA[A/C]TGCCCAGAAGAATAT	80890
rs30401094	snp	A/T	0.415225	0.187619	intron-variant	Trim2	GRCm38.p3	3:84296103	TAAATGAGTCACTTT[A/T]TAAGTGTTGCACAAA	80890
rs30401288	snp	A/G	0.387812	0.208586	intron-variant	Trim2	Mm_Celera	3:84216389	AGGAGAGAAGGCTGC[A/G]TCTGCAATCCTGAGA	80890
rs30402502	snp	C/T	0.444444	0.157135	intron-variant	Trim2	GRCm38.p3	3:84282914	CCAGTTCTGGGGGAT[C/T]CAATGCCCTCTGAGG	80890
rs30408162	snp	G/T	0.5	0	intron-variant	Trim2	GRCm38.p3	3:84176147	AGAAGGAAGTAATGT[G/T]GTGGCAACTAAACAC	80890
rs30409046	snp	A/G	0.444444	0.157135	intron-variant	Trim2, LOC105244477	Mm_Celera	3:84231464	AGTGTCTGTAATGTG[A/G]AGGGCACCGTGCTGG	80890
rs30412313	snp	A/T	0.444444	0.157135	intron-variant, downstream-variant-500B	Trim2, Gm6525	Mm_Celera	3:84175200	CAGAAATTATATATA[A/T]AAAAAAAAAAAGACC	80890
rs30414100	snp	C/T	0.444444	0.157135	intron-variant	Trim2	Mm_Celera	3:84189611	TAACAAACTGTGCAG[C/T]AGCACTCTCAGGCCC	80890
rs30451174	snp	A/C/G	0.444444	0.157135	intron-variant	Trim2	GRCm38.p3	3:84171751	TCTGACCTCACCCCA[A/C/G]CAAGCCTTAGAAGTG	80890
rs30452598	snp	C/G	0.444444	0.157135	intron-variant	Trim2	Mm_Celera	3:84296806	TCTCTGCTTCCCTCT[C/G]CAGTTATTAGCAACC	80890
rs30453058	snp	A/G	0.497778	0.0332592	intron-variant	Trim2, LOC105244477	Mm_Celera	3:84230126	TAATAAGAGGATGGC[A/G]ACTAATCTTGGTTGA	80890
rs30453060	snp	G/T	0.375	0.216506	intron-variant	Trim2	Mm_Celera	3:84284910	TATCATTTTTTGGGA[G/T]AGGGGAAGCTATGTT	80890
rs30455933	snp	A/G	0.444444	0.157135	intron-variant	Trim2	GRCm38.p3	3:84183549	TTGAGTTCCAGGCCA[A/G]ACTGGTCTACAGTAA	80890
rs30458062	snp	C/T	0.375	0.216506	downstream-variant-500B	Trim2	Mm_Celera	3:84159950	AAGAATAGACATACA[C/T]ACTTACCATCAAGCT	80890
rs30460365	snp	C/T	0.375	0.216506	intron-variant	Trim2	Mm_Celera	3:84203594	CTTTCTTTCTTTCTT[C/T]TTTCCTTCCTTCCTT	80890
rs30460922	snp	C/T	0.493827	0.0552116	intron-variant	Trim2	GRCm38.p3	3:84304457	CACCTCCAGGCTAGG[C/T]TTGGTGACTTGGGTC	80890
rs30463736	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Trim2, LOC105244477	Mm_Celera	3:84226786	CTCCATGCCTCTTTG[C/T]TCAGCGGAGAAACCA	80890
rs30470829	snp	A/C/G	0.456747	0.140554	intron-variant, upstream-variant-2KB	Trim2	GRCm38.p3	3:84221503	GTTTCAGTTAAGGAT[A/C/G]GAGAAACCTGACAAA	80890
rs30495308	snp	C/T	0.429688	0.173817	upstream-variant-2KB, intron-variant	Trim2	Mm_Celera	3:84271494	GGCAGCTCATTGTGC[C/T]GAGTCTCTAATCTCA	80890
rs30498405	snp	G/T	0.5	0	intron-variant	Trim2	Mm_Celera	3:84279469	ACTGTAGAAGGCTAA[G/T]CAGTATCTCTGGCTT	80890

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