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
rs6153696	snp	A/C/T	0.5	0	intron-variant	Ddb2	GRCm38.p3	2:91216427	ggtcaagactagctt[A/C/T]gtctatgtagcaaat	107986
rs6243999	snp	C/T	0.5	0	intron-variant	Ddb2	Mm_Celera	2:91221836	ttttgttttgttttt[C/T]gagacagggtttctc	107986
rs6331228	snp	C/T	0.5	0	intron-variant	Ddb2	Mm_Celera	2:91233135	tttgggtatgaactg[C/T]cccctccctgaccca	107986
rs13462681	snp	C/T			synonymous-codon, nc-transcript-variant	Ddb2	Mm_Celera	2:91234240	ATTCCGAAAAGCTGC[C/T]CCCTTTGACAGGAGG	107986
rs27386972	snp	C/T	0.484429	0.0868505	upstream-variant-2KB, nc-transcript-variant	Ddb2, A330069E16Rik	GRCm38.p3	2:91237270	GCCGTAAACCCTGCA[C/T]GCTGGAGGCGGAGCC	107986
rs27386973	snp	C/G	0.124444	0.216185	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	Ddb2, A330069E16Rik	Mm_Celera	2:91236960	CACCTTCGCGCCAAA[C/G]GCTCCTCCGGGCTGC	107986
rs27386974	snp	C/T	0.48	0.0979796	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	Ddb2, A330069E16Rik	GRCm38.p3	2:91236825	GAGCCATGACGTACT[C/T]GGTGAAGAGATATCA	107986
rs27386975	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB	Ddb2, A330069E16Rik	Mm_Celera	2:91236674	CGGAAAGCTAAGGCA[A/G]CAGCACAGGCCGTAC	107986
rs27386976	snp	C/T	0.493827	0.0552116	intron-variant, upstream-variant-2KB	Ddb2, A330069E16Rik	GRCm38.p3	2:91236481	AATAAAACCAGTCGG[C/T]AGCGTGTGGCTCAGT	107986
rs27386977	snp	A/T	0.231111	0.249285	intron-variant, upstream-variant-2KB	Ddb2, A330069E16Rik	Mm_Celera	2:91236452	TAAAACTCTCTGCTG[A/T]CAATGAACTGGCCAA	107986
rs27386978	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Ddb2, A330069E16Rik	Mm_Celera	2:91236207	TCCTTATAGCCCCAG[A/G]TTCAAGTCCTGGTAA	107986
rs27386979	snp	G/T	0.124444	0.216185	intron-variant, upstream-variant-2KB	Ddb2, A330069E16Rik	Mm_Celera	2:91235244	GGAGTTGAGGGACAA[G/T]CTTTTTTGTTGTTGT	107986
rs27386980	snp	C/T	0.124444	0.216185	intron-variant	Ddb2	Mm_Celera	2:91235001	AAATCTCAGGAAAGG[C/T]TCCCCCTGAAAACCC	107986
rs27386981	snp	A/T	0.32	0.24	intron-variant	Ddb2	Mm_Celera	2:91234602	ACTATCTGCAATGTA[A/T]GTGAACTAATCCTGG	107986
rs27386982	snp	A/G	0.32	0.24	intron-variant	Ddb2	Mm_Celera	2:91234549	ATGTCTGGCCCCTTT[A/G]TATACAGGCAATAAG	107986
rs27386983	snp	C/T	0.345679	0.230967	intron-variant	Ddb2	Mm_Celera	2:91228332	GAGGCAAGCCTGATT[C/T]TACAAAATGAGTTCC	107986
rs27386984	snp	A/G	0.244898	0.249948	intron-variant	Ddb2	Mm_Celera	2:91226895	CTGACGCCCTCTTCC[A/G]GCGCATCTGAAGACA	107986
rs27386985	snp	C/G	0.444444	0.157135	intron-variant	Ddb2	Mm_Celera	2:91223476	GCTAAGGGAAGAAGT[C/G]TGCCATAAGTGAAGC	107986
rs27386986	snp	C/T	0.142012	0.225474	intron-variant	Ddb2	Mm_Celera	2:91219204	ACTTTATCACATTTC[C/T]GGCTTACATTCTCAC	107986
rs27386987	snp	G/T	0.142012	0.225474	intron-variant	Ddb2	Mm_Celera	2:91218975	GACAGCACCGAGGCA[G/T]CAACACCAAGGCCAG	107986
rs27386988	snp	C/T	0.142012	0.225474	intron-variant	Ddb2	Mm_Celera	2:91218652	CTGTCTTCCCTGTGC[C/T]GGGCCAAAGTGACAG	107986
rs27386989	snp	A/C	0.142012	0.225474	intron-variant	Ddb2	Mm_Celera	2:91217476	TCACTGTGACAACTC[A/C]AGTATCAAGTATTTG	107986
rs27386990	snp	A/G	0.142012	0.225474	intron-variant	Ddb2	Mm_Celera	2:91217016	GGTGGTGAGAAAGAC[A/G]GGGCACATAAGGAAG	107986
rs27386991	snp	A/G	0.48	0.0979796	utr-variant-3-prime, intron-variant	Acp2, Ddb2	GRCm38.p3	2:91212157	GATACCACTGTCTCC[A/G]AGATATATTTACTGC	107986
rs27386992	snp	C/T	0.42	0.183303	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	Acp2, Ddb2	Mm_Celera	2:91211824	TCCCACAGTATCCCT[C/T]GTCACAAGTGTCCCT	107986
rs27386993	snp	A/G	0.444444	0.157135	utr-variant-3-prime, intron-variant, downstream-variant-500B	Acp2, Ddb2	Mm_Celera	2:91211522	TTTCTGACATCCAAG[A/G]AGCACTCTTACCAGG	107986
rs27386994	snp	C/T	0.18	0.24	utr-variant-3-prime, intron-variant, downstream-variant-500B	Acp2, Ddb2	Mm_Celera	2:91211232	TGGCTATCAAGAACT[C/T]GGGTCATCCAACAGC	107986
rs27386995	snp	C/T	0.197531	0.244432	utr-variant-3-prime, intron-variant, downstream-variant-500B	Acp2, Ddb2	Mm_Celera	2:91211105	GCCTTGCTCTTCCAC[C/T]GAGCCTTGCTCTTTA	107986
rs29500162	snp	A/C	0.48	0.0979796	intron-variant	Ddb2	Mm_Celera	2:91215463	ATATATATATATATT[A/C]TCTTTATATATATAT	107986
rs29874434	snp	A/T	0.5	0	intron-variant	Ddb2	GRCm38.p3	2:91229047	CAGGTGGATCAAAAG[A/T]TCAAGATCAGCCAGG	107986
rs29910435	snp	A/C	0.375	0.216506	intron-variant	Ddb2	Mm_Celera	2:91230632	TTTTGATTTTTTTAA[A/C]ACTTTTTTTTTTTTT	107986
rs29921011	snp	C/T	0.444444	0.157135	intron-variant	Ddb2	Mm_Celera	2:91226794	AATGAAACAGTGGGG[C/T]TGGGGAGATGGCTCA	107986
rs32916553	snp	A/C	0.48	0.0979796	intron-variant	Ddb2	Mm_Celera	2:91215465	ATATATATATATTCT[A/C]TTTATATATATATAT	107986
rs33118915	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Ddb2, A330069E16Rik	GRCm38.p3	2:91236584	AGGCGACAGAAGCCA[A/G]GAACTGCTTCAGAAG	107986
rs33224091	snp	A/C	0.444444	0.157135	intron-variant, upstream-variant-2KB	Ddb2, A330069E16Rik	Mm_Celera	2:91235928	TAAAAATAAGCCGGG[A/C]ATGGTGGCACACGCC	107986
rs33267132	snp	A/G	0.444444	0.157135	intron-variant	Ddb2	Mm_Celera	2:91225700	GCTGGGATTAAAGGC[A/G]TGCACCACTACACCC	107986
rs33577681	snp	A/C	0	0	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Ddb2, A330069E16Rik	Mm_Celera	2:91237096	CCCCGGACTGCCCCA[A/C]CCCCTCGGGCACGGC	107986
rs33653743	snp	A/T	0.5	0	intron-variant	Ddb2	GRCm38.p3	2:91230818	ATCTCCAATTTTGGA[A/T]CTTTTGAAAGTTAGG	107986
rs33890055	snp	G/T	0.444444	0.157135	upstream-variant-2KB, intron-variant	Ddb2, A330069E16Rik	GRCm38.p3	2:91238799	GGAAAACAAAACAAA[G/T]AAATAAGTAAACCCA	107986
rs48414158	snp	A/G			intron-variant	Ddb2	Mm_Celera	2:91222790	AAAAATGACAAGGAC[A/G]TATGGAATAGCCACA	107986
rs211776265	snp	C/T			intron-variant	Ddb2	Mm_Celera	2:91219761	AACCAACCAACCAAG[C/T]CAGGAATAGGAGCAC	107986
rs211848360	snp	A/T			intron-variant	Ddb2	Mm_Celera	2:91233643	ATTCAAGCTACATCG[A/T]GAAATTCTATCTCAA	107986
rs211866635	snp	A/G			intron-variant, upstream-variant-2KB	Ddb2, A330069E16Rik	Mm_Celera	2:91235729	ATCCTAGCACTCAGA[A/G]GCTGCAGCATACTTG	107986
rs212041350	snp	A/C			intron-variant	Ddb2	Mm_Celera	2:91221621	AGAAACACAAGGAAG[A/C]TACAATACCACCTCC	107986
rs212080992	in-del	-/AAC			upstream-variant-2KB	Ddb2	GRCm38.p3	2:91238962	AAAACAAACAAACAA[-/AAC]AACAACAACAACAAC	107986
rs212176234	in-del	-/AAAG			intron-variant	Ddb2	Mm_Celera	2:91220274	GGGAGGGAGGAAAGA[-/AAAG]AAAGAAAGAGAGAGA	107986
rs212463329	snp	C/G			intron-variant	Ddb2	Mm_Celera	2:91214682	TGTTTACTATTATTG[C/G]CAAGCAACCTTATTT	107986
rs212509095	in-del	-/AAAAAAAA			upstream-variant-2KB, intron-variant	Ddb2, A330069E16Rik	Mm_Celera	2:91237648	AAATAAATAAATCTT[-/AAAAAAAA]AAAAAAAAAAAAAAA	107986
rs213142545	snp	A/G			intron-variant	Ddb2	Mm_Celera	2:91223567	GCTGCACAAGTACGC[A/G]ACTGAGTTCAACACC	107986
rs213163106	snp	A/G			upstream-variant-2KB, intron-variant	Ddb2, A330069E16Rik	Mm_Celera	2:91238362	AGCACCAATAATGGG[A/G]ATGTCCTAAGATGTG	107986
rs213201293	snp	C/G			intron-variant	Ddb2	Mm_Celera	2:91224569	TTTTGTGTTATTTTT[C/G]TTTGGCTCTTTAAAA	107986
rs213507097	snp	A/G			intron-variant	Ddb2	Mm_Celera	2:91215546	ACACATTAAATAAAT[A/G]ATATTTAAGAGAAAA	107986
rs213542044	in-del	-/TG			intron-variant, upstream-variant-2KB	Ddb2, A330069E16Rik	Mm_Celera	2:91235281	TTTTGGTTGTTTGTT[-/TG]TTTTTATTTTTCAAG	107986
rs213556552	snp	C/T			intron-variant	Ddb2	Mm_Celera	2:91217273	TGAACCAAAGAGGGG[C/T]GAGGGGATGGGGCGT	107986
rs213585153	snp	A/T			intron-variant	Ddb2	Mm_Celera	2:91232770	ATATACCTCAGCTGC[A/T]AAAAGCACTCGTTGC	107986
rs213694435	snp	C/T			intron-variant	Ddb2	Mm_Celera	2:91226864	TTCTAATCCCAGAAA[C/T]CACCCATAATGAGAT	107986
rs213736436	snp	C/T			upstream-variant-2KB	Ddb2	Mm_Celera	2:91239130	TACACTTTGTTTTGG[C/T]GTGCTTCATGTGTCT	107986
rs213758284	snp	A/G			intron-variant	Ddb2	GRCm38.p3	2:91220412	agcaagcaagcaagc[A/G]agcgagcTGGTCATA	107986
rs213826874	snp	A/C			intron-variant	Ddb2	Mm_Celera	2:91225854	GTACCACCACTGCCC[A/C]ACCTCTTTTTATTTT	107986
rs213996702	snp	C/T			utr-variant-3-prime, intron-variant	Acp2, Ddb2	Mm_Celera	2:91213267	AAGCGGATTTGAGTT[C/T]GAGGCCAGCCTGGTC	107986
rs214044175	snp	A/G			upstream-variant-2KB, nc-transcript-variant	Ddb2, A330069E16Rik	Mm_Celera	2:91238218	ATACAATATGTGTGT[A/G]TCAAAAGTAATGTAT	107986
rs214059032	snp	A/G			intron-variant	Ddb2	Mm_Celera	2:91221966	GCGTGCGCCACCACC[A/G]CCTGGCTTCATCTTG	107986
rs214184635	snp	A/G			intron-variant	Ddb2	Mm_Celera	2:91231002	GCAAAGTAAGACCCC[A/G]TCTTAAAAATAAGAA	107986
rs214186297	snp	A/G			intron-variant	Ddb2	GRCm38.p3	2:91220257	GGAAAAGGAGGAGGA[A/G]GAGGGAGGGAGGAAA	107986
rs214380804	snp	C/G			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	Ddb2, A330069E16Rik	Mm_Celera	2:91236968	CGCCAAACGCTCCTC[C/G]GGGCTGCTTTACTTT	107986
rs214997137	snp	A/C			intron-variant	Ddb2	Mm_Celera	2:91220387	AAGAAAGAAAGAAAG[A/C]AAGCAAGCAAGCAAG	107986
rs215579750	snp	G/T			intron-variant, upstream-variant-2KB	Ddb2, A330069E16Rik	Mm_Celera	2:91235897	CTTCAAGGAAGAGAG[G/T]TAAATCAGAGTATAA	107986
rs215624924	snp	A/G			intron-variant	Ddb2	Mm_Celera	2:91226963	TGGGCCTGAGCAAGC[A/G]CAGTTGACCGAAGGG	107986
rs216063902	in-del	-/TT			intron-variant	Ddb2	Mm_Celera	2:91230635	TGATTTTTTTAAAAC[-/TT]TTTTTTTTTTTTAAT	107986
rs216173882	snp	A/G			intron-variant	Ddb2	Mm_Celera	2:91224851	GCCTCTTAAGTGCTG[A/G]GATTAAAAGCATGAC	107986
rs216197389	in-del	-/T			intron-variant	Ddb2	Mm_Celera	2:91226303	AAGAAAAGTAAATAA[-/T]TTTAAAAAAGCATCT	107986
rs216266876	snp	A/T			intron-variant	Ddb2	Mm_Celera	2:91231312	ATATCCAAAAAATTT[A/T]AGACTTACATTTTTT	107986
rs216409623	snp	A/C			upstream-variant-2KB, intron-variant	Ddb2, A330069E16Rik	Mm_Celera	2:91238623	AAAAAAAAAAAATTA[A/C]AAGCTGGTCAGTGGT	107986
rs216497417	snp	A/G			intron-variant	Ddb2	Mm_Celera	2:91219401	TGCCTAGTATGCACA[A/G]GGCCCTGGGTTTGAC	107986
rs216831095	snp	A/G			intron-variant	Ddb2	Mm_Celera	2:91233384	GCTGTGAGGTGAGCA[A/G]CAAGCACTGCTCCAC	107986
rs216933305	snp	A/G			utr-variant-3-prime, intron-variant	Acp2, Ddb2	Mm_Celera	2:91212232	CTCCACTGCAGCCTC[A/G]GATAGGGCCAGGCTT	107986
rs216962091	snp	A/C			intron-variant	Ddb2	Mm_Celera	2:91223566	TGCTGCACAAGTACG[A/C]AACTGAGTTCAACAC	107986
rs216975718	snp	C/G			upstream-variant-2KB, nc-transcript-variant	Ddb2, A330069E16Rik	Mm_Celera	2:91237947	TCACATCTCAGCAAC[C/G]ACATGGTGGCTCACA	107986
rs217128290	snp	C/T			intron-variant	Ddb2	Mm_Celera	2:91217579	AGGGCTGTGAAAGAG[C/T]ACAGAAAGAGTTGAC	107986
rs217214003	snp	C/T			intron-variant	Ddb2	Mm_Celera	2:91228978	TGACAATGATGACGA[C/T]AAGAAAGAAAAAAGA	107986
rs217220589	snp	A/G			utr-variant-3-prime, intron-variant	Acp2, Ddb2	Mm_Celera	2:91213591	TCTCTTTTTTTAACA[A/G]CTCATAGGTCAAGAA	107986
rs217383458	snp	C/T			intron-variant	Ddb2	Mm_Celera	2:91228330	CAGAGGCAAGCCTGA[C/T]TTTACAAAATGAGTT	107986
rs217523611	snp	C/T			intron-variant	Ddb2	Mm_Celera	2:91225821	CCTCTGCCTCCCAAA[C/T]ACTGGGGTTAATGGC	107986
rs217689020	snp	A/G			intron-variant	Ddb2	Mm_Celera	2:91223521	TGACCCTTATCAATA[A/G]AACAAGAGGGAGGGT	107986
rs217842234	snp	A/G			intron-variant	Ddb2	Mm_Celera	2:91218011	TTCTCAACCTTATGG[A/G]ACAGCCCAGAATAAT	107986
rs218383380	snp	C/T			intron-variant	Ddb2	Mm_Celera	2:91229909	CAAAAACAAAAGCAG[C/T]TCGGTCTGGCACAAA	107986
rs218439549	snp	C/T			intron-variant	Ddb2	Mm_Celera	2:91231515	CCAACACCTTAGAGA[C/T]TGAACATAAATCTTA	107986
rs218496861	snp	A/G			intron-variant	Ddb2	Mm_Celera	2:91221991	ATCTTGTGCATTCTT[A/G]ATGGCAATGCAATTC	107986
rs218712313	snp	A/G			synonymous-codon, nc-transcript-variant	Ddb2	Mm_Celera	2:91234192	CACAGCCAGGGTACT[A/G]GGATGAGTCGGGTGC	107986
rs218736667	snp	A/G			intron-variant	Ddb2	Mm_Celera	2:91223999	TTAAACAACTAGAAA[A/G]ATGAACAAAATACAT	107986
rs218768234	snp	C/G			intron-variant	Ddb2	Mm_Celera	2:91220802	ATTTCAGGACATCAC[C/G]GCTGCCCCCCATCCC	107986
rs218775477	snp	C/T			upstream-variant-2KB, nc-transcript-variant	Ddb2, A330069E16Rik	Mm_Celera	2:91237156	GTAACGTGTGCAGCT[C/T]ACAGGGAGGGTTTTT	107986
rs218797052	snp	A/G			intron-variant	Ddb2	Mm_Celera	2:91225233	TGGGATTAAAGGTGT[A/G]TGCTACCACTGCCTG	107986
rs218833358	snp	A/G			intron-variant, upstream-variant-2KB	Ddb2, A330069E16Rik	Mm_Celera	2:91236287	CTCAGAGCTAACATA[A/G]CCGAGAGGCTATGAA	107986
rs219014716	snp	A/G			intron-variant	Ddb2	Mm_Celera	2:91222290	GGCTGTTCTTACAGA[A/G]GACCTGGGTTCAATT	107986
rs219058476	snp	A/C			utr-variant-3-prime, intron-variant	Acp2, Ddb2	Mm_Celera	2:91213737	GTGGGAGGGAAAAAC[A/C]AACTCTGCCCACTGT	107986
rs219080744	snp	A/T			intron-variant	Ddb2	Mm_Celera	2:91227505	ACAGATAAATCTTTT[A/T]AAAAATGTACTCTAC	107986
rs219129892	snp	A/G			utr-variant-3-prime, intron-variant	Acp2, Ddb2	Mm_Celera	2:91212810	TCCAGCCAAATCAGT[A/G]GGTTCCAGGTACAGT	107986
rs219151307	snp	C/T			intron-variant	Ddb2	Mm_Celera	2:91224931	TGTTTATTTTTCCAT[C/T]TTGGGGTATGTGTGT	107986
rs219358600	snp	A/G			utr-variant-3-prime, intron-variant	Acp2, Ddb2	Mm_Celera	2:91213803	AATAAAAGTGGTTTT[A/G]GTTTTTAAAAGACTT	107986

Full records

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