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
rs3021894	snp	A/G	0.71875	0.0826797	intron-variant	Pafah1b1	GRCm38.p3	11:74704843	GGTATGTGTTCTCCC[A/G]TGACAGCTTTCAGTT	18472
rs3023299	in-del	-/T			upstream-variant-2KB	Pafah1b1	Mm_Celera	11:74724975	GTCTTTCTGTGGATT[-/T]CAGTTTCCAGAATCT	18472
rs3023300	snp	C/T	0.4352	0.167931	intron-variant	Pafah1b1	GRCm38.p3	11:74709216	TCAGCCTCCAAGAGC[C/T]GGGGTGTGTTCTACT	18472
rs3023301	snp	C/T	0.382461	0.212024	intron-variant	Pafah1b1	GRCm38.p3	11:74709010	CTGGTGACTGCCTTT[C/T]CCAGCTGTTTGCTAT	18472
rs3023302	in-del	-/TAGT			intron-variant	Pafah1b1	Mm_Celera	11:74708404	CATAAGTGTGGATAA[-/TAGT]TAGAAACCAGTTGAG	18472
rs3023303	snp	A/G	0.444444	0.157135	intron-variant	Pafah1b1	GRCm38.p3	11:74708366	ACTTTTATAACTTAT[A/G]AGCAGTTGCTGTGAG	18472
rs3023304	in-del	-/AAAC			intron-variant	Pafah1b1	Mm_Celera	11:74708315	TCATACCCTAGAGAA[-/AAAC]AAACATCTTGGGGCT	18472
rs3023305	snp	A/G	0.444444	0.157135	intron-variant	Pafah1b1	GRCm38.p3	11:74704701	AGTCAAGAAATAGTG[A/G]CTGGGCAGTGGTGGC	18472
rs3023306	in-del	-/ACACAC			intron-variant	Pafah1b1	Mm_Celera	11:74704574	AAAAACAAAAAACAA[-/ACACAC]ACACACACACACACA	18472
rs3023307	snp	C/T	0.5	0	intron-variant	Pafah1b1	GRCm38.p3	11:74704476	GACTCGTGTTTGATT[C/T]CCAGAAGCCACATGT	18472
rs3023308	snp	C/T	0.5	0	intron-variant	Pafah1b1	GRCm38.p3	11:74704447	GTTGGCTCATACTAT[C/T]TTACTCCAATCCAGG	18472
rs3023309	snp	C/T	0.399209	0.200591	intron-variant	Pafah1b1	GRCm38.p3	11:74701116	CCAGGCATGTTGATG[C/T]ATTCCTGTAATCCAG	18472
rs3667338	snp	C/T	0.489796	0.070696	intron-variant	Pafah1b1	Mm_Celera	11:74721280	TTGTGATTTTTAAAA[C/T]TGATTCCATCAAATT	18472
rs3679167	snp	A/G	0.5	0	intron-variant	Pafah1b1	GRCm38.p3	11:74701956	AAGCAATGAGCGGAC[A/G]CTTGGAAAAATCTGA	18472
rs3679320	snp	A/G	0.444444	0.157135	intron-variant	Pafah1b1	GRCm38.p3	11:74702038	CTCTTAGTTTTATCT[A/G]ATTAGGTATTTTGCA	18472
rs3691128	snp	G/T	0.433884	0.169371	utr-variant-3-prime, nc-transcript-variant	Pafah1b1	GRCm38.p3	11:74675986	GCTAGACAGTGAGCT[G/T]CTGTCAGAGCCTAAT	18472
rs3692341	snp	C/T	0.495	0.0497494	utr-variant-3-prime, nc-transcript-variant	Pafah1b1	Mm_Celera	11:74676172	GTTATGTCATTGTTT[C/T]TGTTAACCTTTCAAA	18472
rs4139851	snp	A/T	0.5	0	intron-variant	Pafah1b1	GRCm38.p3	11:74702148	ctctctctctctctc[A/T]cacacacacacacac	18472
rs4140077	snp	C/T	0.489796	0.070696	intron-variant	Pafah1b1	Mm_Celera	11:74721225	CAGGACAGCCAGGGA[C/T]ACACAGAGAAACCCT	18472
rs6173900	snp	A/G	0.5	0	intron-variant	Pafah1b1	GRCm38.p3	11:74701738	TTCAAAGACAAGTtg[A/G]ctcaaacctccaatc	18472
rs6362714	snp	C/G	0.498615	0.0262793	intron-variant	Pafah1b1	Mm_Celera	11:74697723	AGACACTATGGCAAA[C/G]TAAAGGATTATTTTT	18472
rs6363729	snp	A/G	0.444444	0.157135	intron-variant	Pafah1b1	Mm_Celera	11:74697882	tgtagagatggctca[A/G]ccatctgctcctctg	18472
rs6364260	snp	A/G	0.498615	0.0262793	intron-variant	Pafah1b1	GRCm38.p3	11:74697960	TTTGTAATGAGATCC[A/G]ATGCCCTCTTCTGGG	18472
rs8236871	snp	C/T	0.1472	0.227886	intron-variant	Pafah1b1	GRCm38.p3	11:74682068	TAGAATGCATTGTTA[C/T]AGAAAATAAATCTAT	18472
rs8236872	snp	A/G	0.142012	0.225474	intron-variant	Pafah1b1	GRCm38.p3	11:74682176	GCATTTACCTTTTTG[A/G]ATCAGATAGACTTGT	18472
rs8236873	snp	C/T	0.459184	0.136902	intron-variant	Pafah1b1	GRCm38.p3	11:74682192	TTGGCATCTTCATTG[C/T]GCATTTACCTTTTTG	18472
rs8236874	snp	A/G	0.142012	0.225474	intron-variant	Pafah1b1	GRCm38.p3	11:74699177	CCTGGGCTACCTGAA[A/G]TCTTATCACAAAAGA	18472
rs8237703	snp	A/G	0.42	0.183303	intron-variant	Pafah1b1	Mm_Celera	11:74709180	TTCTTAGTGTTATGG[A/G]TTTTACTAATTCCTG	18472
rs8237704	snp	C/T	0.595041	0.156807	intron-variant	Pafah1b1	GRCm38.p3	11:74701133	TAAACATTGTTTTCT[C/T]gccaggcatgttgat	18472
rs8237707	in-del	-/T	0.42	0.183303	intron-variant	Pafah1b1	GRCm38.p3	11:74701054	ggccagcttgggctc[-/T]atTTTCTATTTTGTT	18472
rs8239484	snp	A/G	0.375	0.216506	upstream-variant-2KB	Pafah1b1	Mm_Celera	11:74725256	AATACTGTAAAAATC[A/G]CTTGGGAAGCTGCAG	18472
rs8239485	snp	C/T	0.375	0.216506	upstream-variant-2KB	Pafah1b1	Mm_Celera	11:74725374	AGTATAAAATAAACC[C/T]AGTAGCCAAACAAAG	18472
rs8239486	snp	G/T	0.375	0.216506	upstream-variant-2KB	Pafah1b1	Mm_Celera	11:74725475	GCCTCAGGAGCATCC[G/T]TTTTATAAAAAACAA	18472
rs8239487	snp	A/T	0.32	0.24	intron-variant, nc-transcript-variant	Pafah1b1	Mm_Celera	11:74723716	GCTTGAACCCTCAGC[A/T]GCCTGAGTAGCCCAC	18472
rs8239488	snp	A/G	0.32	0.24	intron-variant, nc-transcript-variant	Pafah1b1	GRCm38.p3	11:74723404	CCCCGGTGCGGTGGT[A/G]GTCCAGCCTCTGCAT	18472
rs8239489	snp	G/T	0.32	0.24	intron-variant, nc-transcript-variant	Pafah1b1	GRCm38.p3	11:74723378	TGCATTCAGTAAAGA[G/T]CTGCAGCATCCACCC	18472
rs8239492	in-del	-/T	0.375	0.216506	intron-variant	Pafah1b1	Mm_Celera	11:74679686	CACTAAAACCAGTCC[-/T]TTTTTTTCTTTTTTC	18472
rs8239493	snp	A/G	0.188366	0.242283	utr-variant-3-prime, nc-transcript-variant	Pafah1b1	GRCm38.p3	11:74676896	GAGTTGTATTCTCCA[A/G]ACTGTTGGACTGTGT	18472
rs8254301	snp	C/T	0.165289	0.235211	upstream-variant-2KB	Pafah1b1	Mm_Celera	11:74724591	ATCCCTTGGGAAGCT[C/T]CCCTTTTGCTCTAAA	18472
rs8254302	snp	C/T	0.152778	0.230321	upstream-variant-2KB	Pafah1b1	Mm_Celera	11:74724706	CACTGGCATTTCGGC[C/T]CCTGCTGGCTAGAGC	18472
rs8254303	snp	A/G	0.152778	0.230321	upstream-variant-2KB	Pafah1b1	Mm_Celera	11:74724842	GGCAGAAGAGCTGTT[A/G]AGGTTAAAAGGCAGA	18472
rs8254310	snp	A/G	0.496528	0.0415217	utr-variant-5-prime, nc-transcript-variant	Pafah1b1	GRCm38.p3	11:74699410	TAATTCAAATCCAGG[A/G]ATCACAACTTTTGAT	18472
rs8254311	snp	C/T	0.152778	0.230321	intron-variant	Pafah1b1	GRCm38.p3	11:74699044	CTCACTCTGTAGACC[C/T]GGCTGGCCTCGAACT	18472
rs8254312	snp	A/G	0.142012	0.225474	intron-variant	Pafah1b1	GRCm38.p3	11:74697909	GTTGCTGGGATTTGA[A/G]CTCACGACCTTCAGA	18472
rs8254313	snp	C/T	0.142012	0.225474	intron-variant	Pafah1b1	GRCm38.p3	11:74697822	TGTAGGGGATCTGAA[C/T]TCAGGTCCTAAGACT	18472
rs8254314	snp	A/G	0.142012	0.225474	intron-variant	Pafah1b1	GRCm38.p3	11:74697800	CCTAAGACTTGGATG[A/G]CAAGCAGTTTTCTCA	18472
rs8254315	snp	C/T	0.142012	0.225474	intron-variant	Pafah1b1	Mm_Celera	11:74697758	ccctagcTTGTTTGT[C/T]TTAATCTAGGATGTT	18472
rs8254316	snp	A/T	0.142012	0.225474	intron-variant	Pafah1b1	Mm_Celera	11:74697740	AATCTAGGATGTTAT[A/T]AAAAAATAATCCTTT	18472
rs8254317	in-del	-/T	0.142012	0.225474	intron-variant	Pafah1b1	Mm_Celera	11:74697705	TGCCATAGTGTCTCT[-/T]NATCGTTTATCAGTA	18472
rs8254318	in-del	-/T	0.142012	0.225474	intron-variant	Pafah1b1	Mm_Celera	11:74697704	GCCATAGTGTCTCTN[-/T]ATCGTTTATCAGTAA	18472
rs8254319	snp	C/T	0.152778	0.230321	intron-variant	Pafah1b1	GRCm38.p3	11:74697681	ATCAGTAAAGAATGG[C/T]TTAAGCGAAGAATCG	18472
rs8254320	snp	A/C	0.152778	0.230321	intron-variant	Pafah1b1	GRCm38.p3	11:74697658	AAGAATCGTCATTGG[A/C]CATTAAATCTAGGGG	18472
rs8254321	snp	A/C	0.486111	0.0821678	intron-variant	Pafah1b1	GRCm38.p3	11:74689720	GTAAGACACATAGTG[A/C]TCTTTTTTCAGTTAC	18472
rs8254322	snp	C/T	0.429688	0.173817	intron-variant	Pafah1b1	GRCm38.p3	11:74682212	TGCATAATCGTATTA[C/T]TTCTTTGGCATCTTC	18472
rs8254323	in-del	-/G	0.32	0.24	intron-variant	Pafah1b1	Mm_Celera	11:74682035	AAACCAGTCAGTGCT[-/G]GGGGGTAGGGTCTTA	18472
rs8254326	snp	C/T	0.110727	0.207612	utr-variant-3-prime, nc-transcript-variant	Pafah1b1	GRCm38.p3	11:74675029	ATAGAATTGTGTACT[C/T]GGATGGTTGTTGATT	18472
rs8254327	snp	A/G	0.110727	0.207612	utr-variant-3-prime, nc-transcript-variant	Pafah1b1	GRCm38.p3	11:74674906	TGTAGACATGACCTG[A/G]AGAATAGTTGCTTTT	18472
rs8254328	snp	A/T	0.49948	0.0161206	utr-variant-3-prime, nc-transcript-variant	Pafah1b1	Mm_Celera	11:74674871	TGACATCTTGCACTT[A/T]AGGAGACTAAGACCG	18472
rs8254329	snp	A/G	0.497778	0.0332592	intron-variant	Pafah1b1	GRCm38.p3	11:74681977	GGAGAAAGCTCTTAC[A/G]GACTTGTTTACTTTT	18472
rs8254330	in-del	-/T	0.152778	0.230321	intron-variant	Pafah1b1	Mm_Celera	11:74681885	ctagatagagttaca[-/T]ncagactggtgtgag	18472
rs8254331	in-del	-/A	0.152778	0.230321	intron-variant	Pafah1b1	Mm_Celera	11:74681884	tagatagagttacan[-/A]cagactggtgtgagt	18472
rs13461650	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	Pafah1b1	GRCm38.p3	11:74724178	CTCGAGCCCCGGAAC[A/G]GCCGAGGAGCCCGCC	18472
rs13461651	snp	C/T	0.336735	0.234472	utr-variant-3-prime, nc-transcript-variant	Pafah1b1	Mm_Celera	11:74674482	AAACCCAGTGTGTTG[C/T]TTAATCTAGATGGTG	18472
rs13461652	snp	C/T			utr-variant-3-prime, nc-transcript-variant	Pafah1b1	Mm_Celera	11:74674412	ATTGCAAGAAAGGTT[C/T]TGGGTTTTTTCCAGT	18472
rs16798119	snp	A/G	0.117188	0.211804	intron-variant	Pafah1b1	GRCm38.p3	11:74689754	TAAGTTATAACTTCC[A/G]AGGcattggttctca	18472
rs26904621	snp	C/T	0.231111	0.249285	intron-variant	Pafah1b1	Mm_Celera	11:74716736	AAAGCCTTATACCTG[C/T]AAAATATCCAATGCA	18472
rs26904622	snp	C/T	0.124444	0.216185	intron-variant	Pafah1b1	Mm_Celera	11:74716701	TTAGATATTGTCTGA[C/T]AACCCCTACTCAAAT	18472
rs26904623	snp	C/T	0.493827	0.0552116	intron-variant	Pafah1b1	Mm_Celera	11:74715760	TCTGTGTTAAAAGCA[C/T]ATATATAAGGCCCTA	18472
rs26904624	snp	C/T	0.277778	0.248452	intron-variant	Pafah1b1	Mm_Celera	11:74714512	TACCTACTAGCTATA[C/T]AGAACATACAAATTA	18472
rs26904625	snp	A/G	0.132653	0.220748	intron-variant	Pafah1b1	Mm_Celera	11:74713895	TGTGGTTTAAGAATT[A/G]TCAAGGAGgccgggt	18472
rs26904626	snp	C/T	0.260355	0.249785	intron-variant	Pafah1b1	Mm_Celera	11:74713887	TTAAAAACTGTGGTT[C/T]AAGAATTATCAAGGA	18472
rs26904627	snp	C/G	0.444444	0.157135	intron-variant	Pafah1b1	Mm_Celera	11:74713861	AAAAAGAAAACGAGG[C/G]AGGAAAGGACTTAAA	18472
rs26904628	snp	A/T	0.401235	0.199068	intron-variant	Pafah1b1	Mm_Celera	11:74713099	AGAATTTTGGAGTCA[A/T]GCAACAAAAGTTTAA	18472
rs26904629	snp	A/G	0.124444	0.216185	intron-variant	Pafah1b1	Mm_Celera	11:74712923	TTAAGTTAGTCCCAT[A/G]TTTTGTGTTGCTTAT	18472
rs26904630	snp	G/T	0.495868	0.0452663	intron-variant	Pafah1b1	Mm_Celera	11:74709397	GTTTCTCTTATACTC[G/T]ACACCAAGCAGGATG	18472
rs26904631	snp	C/T	0.387812	0.208586	intron-variant	Pafah1b1	Mm_Celera	11:74709374	TTTATTTCTAGCAGT[C/T]TATCTGAGTTTCTCT	18472
rs26904632	snp	G/T	0.277778	0.248452	intron-variant	Pafah1b1	Mm_Celera	11:74708694	GATGTGAGCTAAATG[G/T]ATTTATTATGTCTTG	18472
rs26904633	snp	C/T	0.231111	0.249285	intron-variant	Pafah1b1	Mm_Celera	11:74707727	GTGGAGTAGGAAGGG[C/T]CTTTAAACAAGTCTG	18472
rs26904634	snp	C/T	0.375	0.216506	intron-variant	Pafah1b1	Mm_Celera	11:74707057	AACAGAAAACATCCA[C/T]GTAAGGGGCTGTGGA	18472
rs26904635	snp	C/T	0.345679	0.230967	intron-variant	Pafah1b1	Mm_Celera	11:74707044	CTTAGGCATGAACAA[C/T]AGAAAACATCCATGT	18472
rs26904636	snp	A/G	0.444444	0.157135	intron-variant	Pafah1b1	Mm_Celera	11:74706840	AGACAAACTCAACTA[A/G]AATGGTCTATAATTA	18472
rs26904637	snp	C/T	0.444444	0.157135	intron-variant	Pafah1b1	Mm_Celera	11:74706665	AAACCTTTTTTCTTT[C/T]AAAACACTGGCATGT	18472
rs26904638	snp	C/T	0.32	0.24	intron-variant	Pafah1b1	GRCm38.p3	11:74706192	TTTGTAATGTGGTCT[C/T]AGAAAGCAAATACAC	18472
rs26904639	snp	A/G	0.32	0.24	intron-variant	Pafah1b1	GRCm38.p3	11:74706059	CACTGCACTGGAATT[A/G]TATGCTATGATAGCT	18472
rs26904640	snp	G/T	0.375	0.216506	intron-variant	Pafah1b1	Mm_Celera	11:74705809	ACAAATGTGATAGTG[G/T]TTTTTTTTTAAGATT	18472
rs26904641	snp	C/T	0.142012	0.225474	intron-variant	Pafah1b1	Mm_Celera	11:74704936	ATGGGACATACACTG[C/T]TTTCTAAAAATAATT	18472
rs26904642	snp	C/T	0.260355	0.249785	intron-variant	Pafah1b1	Mm_Celera	11:74704243	CTTGGCACACTGCTT[C/T]AAACACTCTGGAATA	18472
rs26904643	snp	A/G	0.401235	0.199068	intron-variant	Pafah1b1	Mm_Celera	11:74704232	GTACAGGCACGCTTG[A/G]CACACTGCTTTAAAC	18472
rs26904644	snp	A/G	0.277778	0.248452	intron-variant	Pafah1b1	Mm_Celera	11:74704227	TTCATGTACAGGCAC[A/G]CTTGGCACACTGCTT	18472
rs26904645	snp	C/T	0.132653	0.220748	intron-variant	Pafah1b1	Mm_Celera	11:74703207	TGGAATACGCACTCT[C/T]ATATTGCTTAACTTT	18472
rs26904646	snp	C/G	0.152778	0.230321	intron-variant	Pafah1b1	Mm_Celera	11:74702450	CTGGGTTTTTTCCCT[C/G]CACCAAGAATCACTT	18472
rs26904647	snp	A/C	0.35503	0.226867	intron-variant	Pafah1b1	GRCm38.p3	11:74701231	CTGCCAGTTAAGATG[A/C]CTAAACATTGATGTG	18472
rs26904648	snp	A/G	0.429688	0.173817	intron-variant	Pafah1b1	Mm_Celera	11:74700529	GAGAGGAAGAAAGGC[A/G]AACTGTGTCTAGTAT	18472
rs26904649	snp	G/T	0.484429	0.0868505	intron-variant	Pafah1b1	Mm_Celera	11:74699789	TCCTGGCCCCGTAAG[G/T]GTTTCAGACATAGGT	18472
rs26904650	snp	A/T	0.142012	0.225474	intron-variant	Pafah1b1	Mm_Celera	11:74699248	TTGTCTTTACCACCC[A/T]AAGCCTAGTTAATCA	18472
rs26904651	snp	A/C	0.304688	0.243945	intron-variant	Pafah1b1	Mm_Celera	11:74698701	TCACTTTGCTTTAAA[A/C]TCAAACATGACAAAT	18472
rs26904652	snp	A/G	0.260355	0.249785	intron-variant	Pafah1b1	Mm_Celera	11:74698519	TCACGCCCTGCTCAT[A/G]TCTCTGTTTCTTGAA	18472
rs26904653	snp	C/G	0.415225	0.187619	intron-variant	Pafah1b1	Mm_Celera	11:74693468	GTCCAATGTGGCAGG[C/G]CCTATGAAATCTAAC	18472
rs26904654	snp	C/T	0.197531	0.244432	intron-variant	Pafah1b1	GRCm38.p3	11:74689275	TGACTATGAAGCTTA[C/T]GGTAGTCCAGAACTT	18472
rs26904655	snp	C/T	0.277778	0.248452	intron-variant	Pafah1b1	Mm_Celera	11:74685560	TAGATACTGCAGCAC[C/T]GAACTCTGGCTTCTA	18472

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