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
rs6336113	snp	A/G	0.5	0	intron-variant	Plcg2	Mm_Celera	8:117511611	ctccatggcctctgc[A/G]tcagctcctgcctcc	234779
rs6336591	snp	A/G	0.5	0	intron-variant	Plcg2	Mm_Celera	8:117511682	aacagactgtgattc[A/G]ggntatataagccaa	234779
rs6336594	snp	A/G	0.5	0	intron-variant	Plcg2	Mm_Celera	8:117511685	agactgtgattcngg[A/G]tatataagccaaaga	234779
rs6337314	snp	A/G	0.5	0	intron-variant	Plcg2	Mm_Celera	8:117511857	TGCCCCTTCTGTATC[A/G]GAGCAGCNGAACAAC	234779
rs6337732	snp	C/T	0.5	0	intron-variant	Plcg2	Mm_Celera	8:117511865	CTGTATCNGAGCAGC[C/T]GAACAACGGATGCNG	234779
rs6337773	snp	A/T	0.5	0	intron-variant	Plcg2	Mm_Celera	8:117511879	CNGAACAACGGATGC[A/T]GTTGGCGTTTTGGTT	234779
rs6360944	snp	A/T	0.5	0	intron-variant	Plcg2	Mm_Celera	8:117598732	ACACAGATTCTAATT[A/T]AAAAAATCTTCCAAA	234779
rs6374408	snp	A/G	0.375	0.216506	intron-variant	Plcg2	Mm_Celera	8:117598862	TGCCGCTGCCTCGTA[A/G]CTTTGTGTAGGAAAA	234779
rs13480011	snp	A/G	0.303361	0.244239	intron-variant	Plcg2	Mm_Celera	8:117545016	TTAAAACTCAGTAGC[A/G]AGCTGACAGACAGTT	234779
rs31562224	snp	A/G	0.132653	0.220748	intron-variant	Plcg2	Mm_Celera	8:117546016	AAGATACATTACAGG[A/G]AGACACAGCAAAAGG	234779
rs31562227	snp	A/G	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117546089	AATATAAGGGCCACT[A/G]TAGCATTGAACTTGA	234779
rs31562230	snp	A/G	0.244898	0.249948	intron-variant	Plcg2	Mm_Celera	8:117546839	TACCACTGTGTGCTC[A/G]TGGTTGCCAGCATAC	234779
rs31562233	snp	A/G	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117546877	CCGTGGAAGCAGGAG[A/G]CATGAACGCTCTCTT	234779
rs31563106	snp	C/T	0.32	0.24	intron-variant	Plcg2	Mm_Celera	8:117546892	GCATGAACGCTCTCT[C/T]CTGTTGGCTCTTAGT	234779
rs31563109	snp	A/G	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117546927	TCTCTAGAACTGCGG[A/G]GTCACTTTCTCACCA	234779
rs31563112	snp	A/G	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117547029	CATGCATTCACACAT[A/G]TGTACTCTTGCCCGT	234779
rs31563925	snp	A/G	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117547577	AGAGGTGGCCGGAAT[A/G]TCATCCCCGGTAGCT	234779
rs31563928	snp	C/T	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117547591	TATCATCCCCGGTAG[C/T]TGACGTAACTTTGAC	234779
rs31563931	snp	C/G	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117547853	ACAGGCTTCTCCCCT[C/G]TAGGTACCGGATCCT	234779
rs31564714	snp	C/T	0.18	0.24	intron-variant	Plcg2	Mm_Celera	8:117548089	AAGGAGGTGGGAGCA[C/T]GTGTGTGCACGTGTG	234779
rs31564717	snp	C/T	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117548225	AGAGAGAGCCATGCT[C/T]TAGGTGTGAAGGATA	234779
rs31564720	snp	C/T	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117548713	CTACAAGCAGGAAGC[C/T]CAGCCACGAGCCCCA	234779
rs31564722	snp	A/G	0.231111	0.249285	intron-variant	Plcg2	Mm_Celera	8:117551143	AAGGGAACCCTCCAT[A/G]TACACACACAATCAT	234779
rs31565535	snp	A/G	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117551480	TGTGCCGTTTGTGTC[A/G]TGTTGGTGCCTGTAC	234779
rs31565537	snp	A/G	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117551532	TGAGGTCTGGATGGC[A/G]CATTTTGGGCAGACG	234779
rs31565540	snp	C/T	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117552298	GTTTCTACACTTAGT[C/T]TAAACTCCATTAGGA	234779
rs31565543	snp	A/G	0.231111	0.249285	intron-variant	Plcg2	Mm_Celera	8:117552707	GAGTTGGATGAACCC[A/G]GGACTGTGGAGTCTG	234779
rs31566275	snp	A/T	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117552744	CAACTCTAGGTTCTT[A/T]TCCTAGCCTTAGGTC	234779
rs31566278	snp	A/G	0.391111	0.206368	intron-variant	Plcg2	Mm_Celera	8:117552890	TCAGCTTTGCAGATG[A/G]TCATGTCTTAACGGC	234779
rs31566281	snp	C/T	0.391111	0.206368	intron-variant	Plcg2	Mm_Celera	8:117552910	GTCTTAACGGCACAC[C/T]CTCATAGATGGAGAG	234779
rs31566375	snp	A/C	0.231111	0.249285	intron-variant	Plcg2	Mm_Celera	8:117538692	TACAGAGCTGGCCCA[A/C]TGCCTCACTGTCACA	234779
rs31566377	snp	C/T	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117538928	TCGGAGCAAGGCTTT[C/T]GTGTGGGGCACTCGA	234779
rs31566380	snp	C/T	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117538989	CCTCTAGAGCTTTCT[C/T]CTCCCTCATCCTGAA	234779
rs31566383	snp	C/T	0.32	0.24	intron-variant	Plcg2	Mm_Celera	8:117539153	TCCAAGTACAGCGAC[C/T]TGAGTGTAGGTCCCC	234779
rs31566565	snp	C/T	0.32	0.24	synonymous-codon	Plcg2	Mm_Celera	8:117556048	AGCCAAGGCTGTCCG[C/T]CACAAGGCAGAATGT	234779
rs31566568	snp	C/T	0.32	0.24	intron-variant	Plcg2	Mm_Celera	8:117556200	AGATCATACTTCATG[C/T]CTGCTAATGCATGCT	234779
rs31566571	snp	A/G	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117556413	ATGAAGGTAGTTAAC[A/G]TGGTCACTGAGAGAT	234779
rs31566934	snp	C/T	0.152778	0.230321	intron-variant	Plcg2	Mm_Celera	8:117580346	CGCCTATGAGGTGTG[C/T]GGACTCCTCAGTGAA	234779
rs31566937	snp	C/T	0.277778	0.248452	intron-variant	Plcg2	Mm_Celera	8:117581002	CAAAACATCAAAAGC[C/T]CTCTTAAATAACCTA	234779
rs31566940	snp	C/T	0.165289	0.235211	intron-variant	Plcg2	Mm_Celera	8:117581342	TGATGAAGCATGGGC[C/T]TATTTCTGCTGATAC	234779
rs31566943	snp	A/G	0.165289	0.235211	intron-variant	Plcg2	Mm_Celera	8:117581490	GCTTAGGTAGCTATC[A/G]TGCACATCTTATTGG	234779
rs31566975	snp	C/T	0.231111	0.249285	intron-variant	Plcg2	Mm_Celera	8:117562680	AGTGGGAACTGGTTA[C/T]GGTTCTGAGGAACAC	234779
rs31566978	snp	A/G	0.32	0.24	intron-variant	Plcg2	Mm_Celera	8:117562898	GGGTCTGCAAGGGAT[A/G]TGGAAGGGGAGGCGC	234779
rs31566981	snp	C/T	0.132653	0.220748	intron-variant	Plcg2	Mm_Celera	8:117562980	CAAGCCACACTTGTG[C/T]GGATTCCGTTGCATT	234779
rs31567214	snp	A/G	0.231111	0.249285	intron-variant	Plcg2	Mm_Celera	8:117553046	GGAAGTGTCAGTCAC[A/G]GATGTGAAGGGCTTG	234779
rs31567217	snp	C/G	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117553078	TGATGCAGCCTCCAG[C/G]CCTGGGAAGTGTGAC	234779
rs31567220	snp	A/G	0.32	0.24	intron-variant	Plcg2	Mm_Celera	8:117553168	GATGGATGGAGAACT[A/G]GTTCCTAGCCCTCAA	234779
rs31567222	snp	C/G	0.231111	0.249285	intron-variant	Plcg2	Mm_Celera	8:117553357	GAGTGCTGACTCACG[C/G]TCCAGCAACAGGGAG	234779
rs31567416	snp	C/T	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117539840	TATCTTCTGGCCTTA[C/T]ACTTTGAGACACTAA	234779
rs31567419	snp	A/C	0.32	0.24	intron-variant	Plcg2	Mm_Celera	8:117540041	TAGCTGGAACTTGAC[A/C]TTGGCAGTGCTCTGT	234779
rs31567422	snp	A/T	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117540642	TGCTCAGCACTAAAG[A/T]ATTTTTTATTGGCAT	234779
rs31567484	snp	C/T	0.32	0.24	intron-variant	Plcg2	Mm_Celera	8:117557154	ATAAACTTACATATC[C/T]GGAGATGGGATTTCT	234779
rs31567487	snp	A/G	0.231111	0.249285	intron-variant	Plcg2	Mm_Celera	8:117557401	ATGATTGAGAGGTAC[A/G]CAACCCACTGGCATC	234779
rs31567490	snp	C/T	0.391111	0.206368	intron-variant	Plcg2	Mm_Celera	8:117557431	CATCCTCCTTTGTTC[C/T]AGGGTCTTCGGGAAT	234779
rs31567493	snp	C/G/T	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117557533	GTGGCTAAGAACTCT[C/G/T]CAGTGCTCCACATAA	234779
rs31567706	snp	A/G	0.152778	0.230321	intron-variant	Plcg2	Mm_Celera	8:117581522	GGTTCTGGACCCAAG[A/G]CCTCAGGATGGCGTG	234779
rs31567709	snp	C/T	0.277778	0.248452	intron-variant	Plcg2	Mm_Celera	8:117582038	AAAAGTGACATCTGG[C/T]TGGGCAATAGATTGG	234779
rs31567712	snp	A/C	0.165289	0.235211	intron-variant	Plcg2	Mm_Celera	8:117582133	CTGCTAAGAGGAACA[A/C]AGACACATACTAGTT	234779
rs31567864	snp	C/T	0.231111	0.249285	intron-variant	Plcg2	Mm_Celera	8:117563310	CTCACTTCCTGAGGG[C/T]ATGGTGAAGCAGCCC	234779
rs31567867	snp	C/T	0.32	0.24	intron-variant	Plcg2	Mm_Celera	8:117563369	TGGGGGTCCAGACCC[C/T]GAAGAATGTGCAGTT	234779
rs31567870	snp	A/G	0.260355	0.249785	intron-variant	Plcg2	Mm_Celera	8:117563426	CCTAAACAGCTGCAA[A/G]TAGCAGGGCCCTTGA	234779
rs31567873	snp	C/T	0.391111	0.206368	intron-variant	Plcg2	Mm_Celera	8:117563608	TTGTGAGGTTAGCCG[C/T]GTTTGGAGGCACACA	234779
rs31568244	snp	A/G	0.32	0.24	intron-variant	Plcg2	Mm_Celera	8:117554634	TACTATGAGTTTTAG[A/G]AATTGTGTCCCAAGA	234779
rs31568246	snp	C/T	0.132653	0.220748	intron-variant	Plcg2	Mm_Celera	8:117555064	AGTTGAAGCGAGTGG[C/T]ATTTGGGGCTGTTGG	234779
rs31568249	snp	C/T	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117555116	ACAAGCAGAATTAGT[C/T]ACTGGCATGGGTGGT	234779
rs31568251	snp	A/G/T	0.132653	0.220748	intron-variant	Plcg2	GRCm38.p3	8:117555196	TGCTATGATAGAGTA[A/G/T]TCTGGGTCTTATCCC	234779
rs31568305	snp	A/G	0.165289	0.235211	intron-variant	Plcg2	Mm_Celera	8:117540698	GCGTAACCCATTATG[A/G]CATGTTCATACATGA	234779
rs31568308	snp	A/G	0.142012	0.225474	intron-variant	Plcg2	Mm_Celera	8:117540839	TGACTAGTGGGTTTA[A/G]TTAGGGTTAGTTACA	234779
rs31568310	snp	A/C	0.32	0.24	intron-variant	Plcg2	Mm_Celera	8:117540897	GTGGCTACACCACTA[A/C]AGAAAATGTCTCTTA	234779
rs31568313	snp	A/C	0.142012	0.225474	intron-variant	Plcg2	Mm_Celera	8:117541620	AGCTGACTCTGATTT[A/C]AGTTCGATAGCAAGG	234779
rs31568356	snp	A/G	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117557577	TAGTGTTGAGCCTTG[A/G]CCTTTGGCGTGAAGA	234779
rs31568358	snp	C/T	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117557579	GTGTTGAGCCTTGAC[C/T]TTTGGCGTGAAGAGG	234779
rs31568361	snp	A/C	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117557667	TGAATCTTTCTGTGA[A/C]TATCTGCAAGCATAT	234779
rs31568435	snp	C/G	0.197531	0.244432	intron-variant	Plcg2	Mm_Celera	8:117582264	CAAAGCCTTGCTTTT[C/G]TCTGCCTTTTTTCCT	234779
rs31568438	snp	C/T	0.277778	0.248452	intron-variant	Plcg2	Mm_Celera	8:117582615	CCAGCTCATCTTTGG[C/T]TCTATCCTTCCCAGA	234779
rs31568441	snp	A/G	0.165289	0.235211	intron-variant	Plcg2	Mm_Celera	8:117582809	ACAAACACTTTGACC[A/G]TAAGGTAGAAACTGG	234779
rs31568594	snp	C/T	0.152778	0.230321	intron-variant	Plcg2	Mm_Celera	8:117524990	CGGTAGCAGCCTAGC[C/T]TTGTGTTCCGGTGGC	234779
rs31568597	snp	A/G	0.142012	0.225474	intron-variant	Plcg2	GRCm38.p3	8:117536311	TGTGAGCACATGTCC[A/G]GGCTGTGTGGAGCTG	234779
rs31568599	snp	C/T	0.444444	0.157135	intron-variant	Plcg2	Mm_Celera	8:117536400	GAGCTGGTGTGAGCA[C/T]GTGTCCAGGCTGTGT	234779
rs31568601	snp	C/G	0.132653	0.220748	intron-variant	Plcg2	Mm_Celera	8:117536405	GGTGTGAGCATGTGT[C/G]CAGGCTGTGTGGAGC	234779
rs31568666	snp	A/G	0.260355	0.249785	intron-variant	Plcg2	Mm_Celera	8:117564288	ATGAAGAAGCACAGG[A/G]TGTGCAGGCAACAGG	234779
rs31568669	snp	A/G	0.260355	0.249785	intron-variant	Plcg2	Mm_Celera	8:117564421	GGAATGAAGATCCAG[A/G]GAGTCAAATCTGCTT	234779
rs31568672	snp	C/T	0.132653	0.220748	intron-variant	Plcg2	Mm_Celera	8:117564583	TACTCCTGTTAGGTA[C/T]GTGTTTCTAGAGATG	234779
rs31568936	snp	G/T	0.197531	0.244432	intron-variant	Plcg2	Mm_Celera	8:117587925	AAGAATGAAATTATA[G/T]CATTTACATGTGGAG	234779
rs31568939	snp	A/C/T	0.277778	0.248452	intron-variant	Plcg2	Mm_Celera	8:117589014	GATCTGATCTGCTGC[A/C/T]GACTGTCAATGCAGC	234779
rs31568942	snp	A/T	0.336735	0.234472	intron-variant	Plcg2	Mm_Celera	8:117589378	GACCTGCTTGCCTTC[A/T]GCCTTCTGGTCTTGT	234779
rs31569134	snp	A/C	0.165289	0.235211	intron-variant	Plcg2	Mm_Celera	8:117582886	ACAGCCTCAATGACG[A/C]TACTCCAGGAACCAC	234779
rs31569137	snp	A/G	0.165289	0.235211	intron-variant	Plcg2	Mm_Celera	8:117582940	ATAGCCATGTATGTG[A/G]CTAAGAAAATGGCCC	234779
rs31569140	snp	A/T	0.165289	0.235211	intron-variant	Plcg2	Mm_Celera	8:117583257	AATATTTTATAATGA[A/T]TGGCTCACTAGAAGG	234779
rs31569143	snp	C/T	0.165289	0.235211	intron-variant	Plcg2	Mm_Celera	8:117583294	TCAGGAAGTGTGTCA[C/T]GTTCTGCAAGTCTGT	234779
rs31569214	snp	C/T	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117555348	ACACAGCAGAGACAA[C/T]CCACTAAGATATGTT	234779
rs31569217	snp	C/G	0.231111	0.249285	intron-variant	Plcg2	Mm_Celera	8:117555604	GTTCTAAACCTGTCA[C/G]TTGACCAGTTCATCG	234779
rs31569219	snp	C/T	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117555809	TTGGTTTCCTGTCCA[C/T]ACTCAGGAGAATTGG	234779
rs31569222	snp	G/T	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117555857	GACTCTGGTCAGAGA[G/T]GGACTCACAGCTGTC	234779
rs31569224	snp	C/T	0.32	0.24	intron-variant	Plcg2	Mm_Celera	8:117557689	CAAGCATATAAATAT[C/T]TGTTCATATACATTC	234779
rs31569227	snp	C/T	0.124444	0.216185	intron-variant	Plcg2	Mm_Celera	8:117557809	ACACCTTCCCACATA[C/T]ACCACTCTTTCTTCT	234779
rs31569229	snp	A/G	0.231111	0.249285	intron-variant	Plcg2	Mm_Celera	8:117557931	TCAGCCACAGGTGGA[A/G]TCTTGTTACCAAGCA	234779
rs31569230	snp	A/G	0.260355	0.249785	intron-variant	Plcg2	Mm_Celera	8:117558237	TCTGGGGTTGACGGT[A/G]ACCCAGAATGATTGA	234779
rs31569232	snp	C/T	0.32	0.24	intron-variant	Plcg2	Mm_Celera	8:117558295	CTCCTGTCGTGCTGC[C/T]GAGGTGACATTTGAC	234779
rs31569296	snp	C/G	0.132653	0.220748	intron-variant	Plcg2	Mm_Celera	8:117541843	TTCTGGGTGTTGGCT[C/G]TATCTTGGACTGGGT	234779

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