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
rs3661743	snp	A/G	0.48	0.0979796	intron-variant	Dtx2	Mm_Celera	5:136019811	GTGGAACTTTGTAGA[A/G]CAGGCTGACCTCAAA	74198
rs3661767	snp	C/T	0.48	0.0979796	intron-variant	Dtx2	Mm_Celera	5:136019829	GGCTGACCTCAAACT[C/T]AGAGATCCACCTGCC	74198
rs3662806	snp	C/T	0.5	0	intron-variant	Dtx2	Mm_Celera	5:136019955	CTTTAGCCCAGCCCC[C/T]GTTGGGTGTGTGGCT	74198
rs3665722	snp	G/T	0.5	0	intron-variant, upstream-variant-2KB	Dtx2	Mm_Celera	5:136013889	GTACTGTGTGCACAT[G/T]CTTGCCTGGTGCCGG	74198
rs3666316	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Dtx2	Mm_Celera	5:136013990	CTCTGGAAGAGCAGC[C/T]ATTGCTTTTAACTGT	74198
rs3704201	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Dtx2	Mm_Celera	5:136014237	GAAATCCGCCTGCCT[C/T]TGCCTCCCAAGAGCT	74198
rs4136167	snp	A/G	0.5	0	intron-variant	Dtx2	Mm_Celera	5:136020064	CTGGGGGCAGAGCCT[A/G]GAGGCAGTGGTTGGT	74198
rs6220833	snp	A/G	0.5	0	intron-variant	Dtx2	GRCm38.p3	5:136009673	ggggtcagctctcac[A/G]ccccggggctggctc	74198
rs6221958	snp	A/T	0.5	0	intron-variant	Dtx2	Mm_Celera	5:136009946	tcaaaagaacaaaAG[A/T]AAAGGTTTTCTTTAG	74198
rs6222444	snp	A/G	0.5	0	intron-variant	Dtx2	Mm_Celera	5:136009997	TGTGTGTGAGTAAAT[A/G]CTGTGTCTTTTTCTA	74198
rs6343532	snp	C/G	0.5	0	intron-variant	Dtx2	Mm_Celera	5:135995973	TCAGGATTGACTTCA[C/G]TTGGTCAAGGTGTCA	74198
rs29500922	snp	A/G	0.48	0.0979796	intron-variant	Dtx2	Mm_Celera	5:135997381	CTTCTTCACCCTTCC[A/G]TTTCAAACACAAGTC	74198
rs29525988	snp	C/T	0.5	0	intron-variant	Dtx2	Mm_Celera	5:136028144	TCACTGAAGTGTCCT[C/T]GGAAGTGCTGGCAGT	74198
rs29526427	snp	C/G/T	0.5	0	intron-variant	Dtx2	GRCm38.p3	5:136019567	AAGAGGTAGAAACAG[C/G/T]TTAGGGAAGGGTGGA	74198
rs29528303	snp	A/G	0.5	0	intron-variant	Dtx2	Mm_Celera	5:136024258	CTCATCCCCACGCCC[A/G]AGATCTTTCTTTATC	74198
rs29528847	snp	C/T	0.444444	0.157135	intron-variant	Dtx2	Mm_Celera	5:135999554	GCATAGAGTATCAAA[C/T]TTTGATCGACACTCC	74198
rs29541873	snp	A/G	0.444444	0.157135	intron-variant	Dtx2	Mm_Celera	5:136003779	CCAGGCTGGTCAGCC[A/G]GCTGCCTCCCAGGAT	74198
rs29543430	snp	C/T	0.5	0	intron-variant	Dtx2	Mm_Celera	5:136029307	TATGGTGTCGCATAC[C/T]TGTGTAGTTTGGAAG	74198
rs29570031	snp	C/T	0.48	0.0979796	intron-variant	Dtx2	Mm_Celera	5:136018736	CAGAGTCCTTGTCTC[C/T]TATTCTCAGCTGCAT	74198
rs29625577	snp	C/G	0.5	0	intron-variant	Dtx2	Mm_Celera	5:136016301	CAGCCAAGGGAGGGT[C/G]AGTGGTACTAGGTGA	74198
rs29628798	snp	C/T	0.5	0	intron-variant	Dtx2	Mm_Celera	5:136023203	TGTCTAGCCCAGTGC[C/T]TCAACCTCCTGACTG	74198
rs29630431	snp	C/T	0.375	0.216506	intron-variant	Dtx2	GRCm38.p3	5:136030352	TCAGGCCTTTGTACA[C/T]GGTGTACTTTGTCTA	74198
rs29636384	snp	G/T	0.444444	0.157135	intron-variant	Dtx2	Mm_Celera	5:136003119	GGCGGCACCTGGGTG[G/T]TTTGCTTTTCTTGGA	74198
rs29686390	snp	C/T	0.5	0	intron-variant	Dtx2	Mm_Celera	5:136020493	CACATGTACTTGTAT[C/T]TGCTGATTCGTGTGC	74198
rs29728166	snp	A/G	0.48	0.0979796	intron-variant	Dtx2	Mm_Celera	5:136018046	GATCCAGCTCTGGTC[A/G]TCAGGCCTGGCGGCA	74198
rs29730009	snp	A/T	0.5	0	intron-variant	Dtx2	Mm_Celera	5:136025080	AGCCTACTCATTTCC[A/T]AATTGAGAGCGGTGG	74198
rs29732642	snp	A/G	0.5	0	intron-variant	Dtx2	Mm_Celera	5:136019526	CCTTGGCTGCATGTC[A/G]CCATAGCTAAAGGAA	74198
rs29778385	snp	A/G	0.375	0.216506	intron-variant	Dtx2	Mm_Celera	5:136017328	ATGCGCTCCCTTACC[A/G]CACTGCAAGTGCAGA	74198
rs29817701	snp	A/G	0.5	0	intron-variant	Dtx2	Mm_Celera	5:136022413	TGAGTATGAGTGTGG[A/G]TGGATCCAGAGGACT	74198
rs32247734	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136019696	GAGAGGACAGGAAGC[C/T]CCATCACACGAGGCT	74198
rs32247735	snp	A/T			intron-variant	Dtx2	Mm_Celera	5:136020168	TGAGAAGGTTTTGTA[A/T]TCTTCACATTTCATC	74198
rs32247736	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136020290	TGTTCTCAAAGTAGA[A/G]CTCTACCAAACCCAG	74198
rs32247737	snp	C/T	0.5	0	intron-variant	Dtx2	Mm_Celera	5:136020674	CAGGTGGGCCATAAA[C/T]CTCCATGTGTAACTC	74198
rs32247738	snp	C/T	0.5	0	intron-variant	Dtx2	Mm_Celera	5:136020937	CTGTGACTTCAGGTT[C/T]CTCTTGGGGCCTCTG	74198
rs32247739	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136021135	TGCGTAGTGTACGAT[A/G]CTGACTTTGCCACTG	74198
rs32247740	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136021395	TTTCTTTTGCATGTA[C/T]TTATTTAGTGTGTAG	74198
rs32247741	snp	A/C			intron-variant	Dtx2	Mm_Celera	5:136023488	ATACCAAAACAGAGA[A/C]ACAAAGAGTCACTTA	74198
rs32247742	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136023638	TTAAGGGGGATACAC[C/T]GTCATTCTTAGCAAG	74198
rs32247743	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136023743	AACTGAGTTTGTGTT[A/G]GTAAGTAGGCCCCTA	74198
rs32248634	snp	A/G	0.444444	0.157135	intron-variant	Dtx2	Mm_Celera	5:136023779	GCACTTGGGTAGTTA[A/G]ATGTGCAAACTTATG	74198
rs32248635	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136023802	AACTTATGGGCAGGC[A/G]CGTCACATACAGCCT	74198
rs32248636	snp	A/G			intron-variant	Dtx2	GRCm38.p3	5:136023994	ACAGTGACAAAAGGC[A/G]TGGTCCTTGGTGTTC	74198
rs32248637	snp	C/T	0.5	0	intron-variant	Dtx2	Mm_Celera	5:136024553	ATGTGGGGTCTCACC[C/T]ACAATGTGTACAGTG	74198
rs32248638	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136025240	TGGCTAAGAAGCCAG[A/G]GCATCCATTCCTGGA	74198
rs32248639	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136025258	ATCCATTCCTGGAAG[A/G]AGGGCCTTTGGAATC	74198
rs32248640	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136025672	GACTTGTCTCGGTTT[A/G]AAGACGTGCTACAGA	74198
rs32248641	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136025679	CTCGGTTTAAAGACG[C/T]GCTACAGAAGGCAGC	74198
rs32248642	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136025992	CCAAGTGGCTCTAGC[A/G]AAGAGTCAAGGGAAG	74198
rs32248643	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136026038	AGCCAGCGCTGCTGG[A/G]ACTACCTCCTGTTGC	74198
rs32249115	snp	C/T			upstream-variant-2KB	Dtx2	Mm_Celera	5:135992819	CGTGAATTCAGTTGA[C/T]TTAAGGCAGATTTAG	74198
rs32249116	snp	A/T			upstream-variant-2KB	Dtx2	Mm_Celera	5:135993089	ATGCCTTAGGTTTGA[A/T]CCCAGGACTCACGTG	74198
rs32249117	snp	C/G			upstream-variant-2KB	Dtx2	Mm_Celera	5:135993822	ACACTGCTGAGGCCA[C/G]GCCTCCTTGACTTCT	74198
rs32249118	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	Dtx2	Mm_Celera	5:135994932	CGGAGGTCGGCGGTC[C/T]TCTCAACCTGTTCCT	74198
rs32249119	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:135995459	GTGTCAGACTGGGTC[C/T]CTGGGGCACTTTGGG	74198
rs32249120	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:135995543	GTTGCCCGCGTTAGC[C/T]TTGCCTCCACAGTGG	74198
rs32249121	snp	A/T			intron-variant	Dtx2	Mm_Celera	5:135996050	TCTCTGGTGTGTTGA[A/T]TTCCTTCATGGACCA	74198
rs32249122	snp	A/T			utr-variant-5-prime, intron-variant	Dtx2	Mm_Celera	5:135996346	TTTGCCGGGTTCTTG[A/T]TTGCTGTTCCTATCA	74198
rs32249123	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:135997766	AGTGTTCATTTCTTT[A/G]TTTGCACAAACCTCT	74198
rs32249594	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136026301	GTGGTCTGGGAGGCA[C/T]TGGTACCCTTCCTTG	74198
rs32249595	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136026787	TTGGGTGATGGGCTT[A/G]TCACCCAGGACAACT	74198
rs32249596	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136027154	AATGATGGTAACTGA[A/G]GCTCCTTTCAGCTCT	74198
rs32249597	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136027274	AGACCTGTAGCCACA[A/G]ACCAGTTTTTGAGAC	74198
rs32249598	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136027436	TTGCCAGTGGCCAGA[A/G]TGTAAGTGTATGCAG	74198
rs32249599	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136027740	GGTCTCATGGCCCAG[C/T]TCTTGGTTATAAACC	74198
rs32249600	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136027754	GCTCTTGGTTATAAA[C/T]CTGTAGCCATGGCTG	74198
rs32249601	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136028003	GATCGCTCAGCTAAC[A/G]AGCCCAGTGGGCTTG	74198
rs32249602	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136028996	GGCAGGACTTTGTAC[C/T]TTGTGCTGGCTCACT	74198
rs32249603	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136030067	AGTCAGACAAACAAA[C/T]GCGTCTCTCTTGGGT	74198
rs32249794	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:135997790	AACCTCTGCTGGGTG[C/T]CAGACGAGATCTCTG	74198
rs32249795	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:135997838	TGGGCGGAAAGACAG[A/G]TGCACCAGTTAGTGA	74198
rs32249796	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:135997894	GAGCTAAGGTGAATC[A/G]TGAGGTGAACCCCTC	74198
rs32249797	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:135998098	GAACAACTGAGTGAC[C/T]GTGGAGTGGAGAGGC	74198
rs32249798	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:135998184	TCAAAGATGTGCATA[C/T]CCAGGAACCTGGTCT	74198
rs32249799	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:135998217	AGTGTGCTTGTGGTT[C/T]TGTGCAGCCTTTACA	74198
rs32249800	snp	A/C			intron-variant	Dtx2	Mm_Celera	5:135998553	GGGCTGTCTCCATAA[A/C]TGAGCGCCAATTCAA	74198
rs32249801	snp	A/G			intron-variant	Dtx2	GRCm38.p3	5:135999390	CCTGCATCTAGATCC[A/G]TGCACACACAGAGTT	74198
rs32249802	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136000673	CTGCCTTAATACTCA[C/T]GCATTGTTCTCCGTG	74198
rs32249803	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136000685	TCACGCATTGTTCTC[C/T]GTGCATGTCTGCTTT	74198
rs32250574	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136001395	CTGAGTCATCTCATT[A/G]CCCATTATGGTTTTG	74198
rs32250575	snp	C/T			intron-variant	Dtx2	GRCm38.p3	5:136001526	GTGCAGGTGCAGTTG[C/T]AGGTGCTACGGTGCA	74198
rs32250576	snp	G/T			intron-variant	Dtx2	Mm_Celera	5:136001836	GCGATTTGTCTGTCT[G/T]TGTCTCCAACTGTGC	74198
rs32250577	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136001857	CCAACTGTGCCCTGC[A/G]CCATCTTGATCTCTA	74198
rs32250578	snp	C/T	0.444444	0.157135	intron-variant	Dtx2	Mm_Celera	5:136001924	ATTGTTGGTTTTAGT[C/T]TTTCTCCAAGTTTGC	74198
rs32250579	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136002829	AGCAGCTTGCTGCTA[A/G]TTTTTTTCCTTTTCT	74198
rs32250580	snp	G/T			intron-variant	Dtx2	Mm_Celera	5:136004243	AGCTGAGGTTAGGTG[G/T]GCTCCCCGGTAGATG	74198
rs32250581	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136004549	TTCTCCACCCTCCTC[C/T]GCACCAATTTTTAAT	74198
rs32250582	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136004926	GAGGCTTTCTTAGCC[C/T]CTGAAAAGTCTCTTC	74198
rs32250583	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136005042	AGATGACTTAGAAAA[C/T]GGCTCAAAGAATAAA	74198
rs32250654	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136030387	ACACCACTGAGGTCC[A/G]CTTGCCTTGTGGAGA	74198
rs32250655	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136030434	CGTCAGCCATGTTGA[C/T]CTCTCCCGCCATCTG	74198
rs32250656	snp	C/T			synonymous-codon	Dtx2	Mm_Celera	5:136030599	AGGCCATGAAGACTG[C/T]GGGACTATACTCATT	74198
rs32250657	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136030696	TCTTCCTGCCCAGCA[C/T]TCTCTCAGCATCTGT	74198
rs32250658	snp	C/T			intron-variant	Dtx2	Mm_Celera	5:136030766	GGAGTGATGGGAGTC[C/T]TTCCTTCACCTCTCT	74198
rs32250659	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136030860	AGCACTATGTTGGAG[A/G]CTGGAGAATTGGGGG	74198
rs32250660	snp	G/T			intron-variant	Dtx2	Mm_Celera	5:136031173	GCATCATGCTGTCCT[G/T]TTCCTTTCACAGGGA	74198
rs32250661	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136031333	AGACTCAACCTGAAC[A/G]GCAGCTCCAGGGAGG	74198
rs32250662	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136031440	TCAGCAAGGACTTAG[A/G]GTCGAGGAAGAGGCT	74198
rs32250663	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136031484	AATAGCTGACTTGTG[A/G]GCTTGGATATAGGCC	74198
rs32251504	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136031854	TGGCTTTCATGTGGA[A/G]ATCGTAAAACAGCTC	74198
rs32251505	snp	A/G			intron-variant	Dtx2	Mm_Celera	5:136031957	GCCATCTTGCTAGCC[A/G]CCTTGTCTTCATCCC	74198

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