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
rs4223630	snp	A/T	0.21875	0.248039	intron-variant	Plcg1	Mm_Celera	2:160762712	TGCCCATGGCTGGGT[A/T]CACTACCCAGCCTGA	18803
rs4223631	snp	C/T	0.21875	0.248039	intron-variant	Plcg1	Mm_Celera	2:160762723	GGGTACACTACCCAG[C/T]CTGAAAGATACAGGG	18803
rs4223632	snp	C/G	0.21875	0.248039	intron-variant	Plcg1	Mm_Celera	2:160762867	GAACAGCAGCTCTAT[C/G]GGGTGTTGTACTGGG	18803
rs4223633	snp	A/G	0.21875	0.248039	intron-variant	Plcg1	Mm_Celera	2:160762868	AACAGCAGCTCTATG[A/G]GGTGTTGTACTGGGA	18803
rs4223634	snp	C/T	0.21875	0.248039	intron-variant	Plcg1	Mm_Celera	2:160762889	TGTACTGGGAGAGGG[C/T]ACTGTCAAGAAGGGT	18803
rs4223635	snp	A/G	0.172336	0.23763	intron-variant	Plcg1	Mm_Celera	2:160762976	TGACAAAGACGACTC[A/G]ATATGCTTCCCCTTA	18803
rs6219572	snp	C/T	0.244898	0.249948	intron-variant	Plcg1	Mm_Celera	2:160764427	ACAGCTTGGTTAACA[C/T]TGCTTTGCACCCATT	18803
rs6220109	snp	C/T	0.5	0	intron-variant	Plcg1	Mm_Celera	2:160764517	GAGAAATACTGTTGT[C/T]AGGGCTTTGCTCCCT	18803
rs6221697	snp	A/G	0.5	0	intron-variant	Plcg1	Mm_Celera	2:160758282	GCACCCAAAAGAACA[A/G]ACTCAAGACAGGATT	18803
rs6234534	snp	A/G	0.5	0	intron-variant	Plcg1	Mm_Celera	2:160764834	TGCCCCTAACAGAGA[A/G]AGCTGGGGCCTCACT	18803
rs6235637	snp	C/T	0.5	0	intron-variant	Plcg1	Mm_Celera	2:160765044	CTTAGAGGCTTTCCC[C/T]ACCTAGGATATAAAT	18803
rs13476878	snp	C/T	0.495605	0.0466686	intron-variant	Plcg1	Mm_Celera	2:160769245	TTGGTACCCAAAGCC[C/T]TTCCCTGGAGTGCCT	18803
rs27303530	snp	C/T	0.231111	0.249285	synonymous-codon, intron-variant	Plcg1, Zhx3	Mm_Celera	2:160774531	TTCCTCTTTCAGTAC[C/T]TCAGATGGTCCTTCC	18803
rs27303531	snp	C/T	0.124444	0.216185	intron-variant	Plcg1, Zhx3	Mm_Celera	2:160773135	TAAGAGACTAGGAAC[C/T]AGGCAGGGTGGTAGT	18803
rs27303532	snp	A/T	0.231111	0.249285	intron-variant	Plcg1, Zhx3	Mm_Celera	2:160771872	TCCTGTCACTCACCT[A/T]GCCCATCATCCTGGC	18803
rs27303533	snp	C/T	0.124444	0.216185	intron-variant	Plcg1, Zhx3	Mm_Celera	2:160771668	CCATGGCAGCTACAA[C/T]GTGTACAGTCCCCAG	18803
rs27303534	snp	A/G	0.42	0.183303	intron-variant, utr-variant-3-prime	Plcg1, Zhx3	GRCm38.p3	2:160771442	GCTATTTGCTCAGAA[A/G]TGTCAGGCGGAAGGT	18803
rs27303535	snp	A/G	0.32	0.24	intron-variant, utr-variant-3-prime	Plcg1, Zhx3	Mm_Celera	2:160771352	TCTGGGTCTAGGTAT[A/G]TGCAATCTGAATTGT	18803
rs27303536	snp	C/T	0.391111	0.206368	intron-variant, utr-variant-3-prime	Plcg1, Zhx3	GRCm38.p3	2:160771048	AGAACACAAGACAAG[C/T]CTGGCACAAAATGTG	18803
rs27303537	snp	A/G	0.124444	0.216185	intron-variant, utr-variant-3-prime	Plcg1, Zhx3	GRCm38.p3	2:160770952	ATTACAGTTAACTAA[A/G]GAGAATGGTTAGCAT	18803
rs27303538	snp	C/T	0.165289	0.235211	intron-variant, utr-variant-3-prime	Plcg1, Zhx3	GRCm38.p3	2:160770611	TGCCAGGAACTCTGA[C/T]CTGCAGGTCTTTGTG	18803
rs27303539	snp	C/T	0.32	0.24	intron-variant, utr-variant-3-prime	Plcg1, Zhx3	GRCm38.p3	2:160770533	ATCTGTCCAGTGATG[C/T]CCAGCACCTCTGGAT	18803
rs27303540	snp	C/T	0.32	0.24	intron-variant	Plcg1, Zhx3	Mm_Celera	2:160770264	AGAGGTAAGTGGGGC[C/T]ATGATGACACATCCT	18803
rs27303541	snp	C/T	0.32	0.24	intron-variant	Plcg1, Zhx3	Mm_Celera	2:160770191	CCTGGAAGTTGACCA[C/T]TGCTTCTTGGTTTTC	18803
rs27303542	snp	A/G	0.244898	0.249948	intron-variant	Plcg1, Zhx3	Mm_Celera	2:160770082	GTTCCAGGGCCCTGG[A/G]TTACAAAAAAAAGCC	18803
rs27303543	snp	A/G	0.32	0.24	intron-variant	Plcg1	Mm_Celera	2:160769843	TTCTGTTCTCTGAAG[A/G]AAAACAATCACTCAC	18803
rs27303544	snp	C/T	0.32	0.24	intron-variant	Plcg1	Mm_Celera	2:160769720	CATGAAGCTCAAATG[C/T]ACATCAGTTGTACGA	18803
rs27303545	snp	G/T	0.32	0.24	intron-variant	Plcg1	Mm_Celera	2:160769494	TGTCCACCAAGTAAC[G/T]TAATGTTTCTGTTCC	18803
rs27303546	snp	C/T	0.197531	0.244432	intron-variant	Plcg1	Mm_Celera	2:160769471	GCTGCTCTCTGTGTC[C/T]TGCATAATGTCCACC	18803
rs27303547	snp	A/G	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160769362	CTTGTTTCTTACCTG[A/G]ACAATCTTGCCATTA	18803
rs27303548	snp	C/T	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160769201	ATCTGCCAACCTACA[C/T]CCCAACTCCTCTGTC	18803
rs27303549	snp	C/T	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160768822	CATCTAGGGAAAGGA[C/T]TCCCAACACTAACAC	18803
rs27303550	snp	A/G	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160768521	AGATGTCCTAGGGCC[A/G]GCAGGGAGGAAGGGA	18803
rs27303551	snp	A/C	0.32	0.24	intron-variant	Plcg1	Mm_Celera	2:160768441	TCACCTAGAGGACAA[A/C]ACGAGTCTCCAACCA	18803
rs27303552	snp	C/T	0.152778	0.230321	intron-variant	Plcg1	Mm_Celera	2:160768297	TAGGATTTCCTTGGC[C/T]GGCTTCCCAGAAAGT	18803
rs27303553	snp	C/T	0.152778	0.230321	intron-variant	Plcg1	Mm_Celera	2:160768165	GATAGGATGAGCTGA[C/T]CAAAGACCTTTATGT	18803
rs27303554	snp	C/T	0.142012	0.225474	intron-variant	Plcg1	Mm_Celera	2:160767811	AGATAGTACGATCGT[C/T]AGTTCTGTCATTAGT	18803
rs27303555	snp	G/T	0.152778	0.230321	intron-variant	Plcg1	Mm_Celera	2:160766980	GCTTTATCCTAGGCA[G/T]TTTACCTTCAACTCA	18803
rs27303556	snp	A/G	0.142012	0.225474	intron-variant	Plcg1	Mm_Celera	2:160766882	ACGTAATAGACTTCC[A/G]CCCACTGGACATGTC	18803
rs27303557	snp	A/G	0.152778	0.230321	intron-variant	Plcg1	Mm_Celera	2:160766811	AAGACCAAGATGTGT[A/G]GACAGGAGCTAGGGG	18803
rs27303558	snp	A/G	0.142012	0.225474	intron-variant	Plcg1	Mm_Celera	2:160765271	ACCTGAGCTGGCCTT[A/G]GGAAAGAGCAGATCA	18803
rs27303559	snp	C/T	0.152778	0.230321	intron-variant	Plcg1	Mm_Celera	2:160764368	ACCCATCTTGGTGCC[C/T]CGTGGCTGTCTTGCC	18803
rs27303560	snp	C/T	0.32	0.24	synonymous-codon	Plcg1	Mm_Celera	2:160759872	CATGTGGATCTGCGG[C/T]AGCCAGCTTGTAGCA	18803
rs27303561	snp	A/G	0.152778	0.230321	synonymous-codon	Plcg1	Mm_Celera	2:160759830	TAAGGGCCAGAGGCT[A/G]GACTCCTCCAATTAT	18803
rs27303562	snp	A/G	0.152778	0.230321	synonymous-codon	Plcg1	Mm_Celera	2:160759803	CCGGCTGCAGCTCTC[A/G]CGCATCTACCCTAAG	18803
rs27303563	snp	A/G	0.21875	0.248039	intron-variant	Plcg1	Mm_Celera	2:160758725	TCCATTGAGCCTGGC[A/G]AAGCATTTGTAGATG	18803
rs27303564	snp	C/T	0.152778	0.230321	intron-variant	Plcg1	Mm_Celera	2:160758319	GATGGGCTTAGGAAA[C/T]GTTGAGCATTAAGTA	18803
rs27303565	snp	C/T	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160756324	TGGGTGGCCAAGAAT[C/T]TCCCTGGAGAAAACC	18803
rs27303566	snp	C/T	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160756250	GTGCACTTACTCTTA[C/T]TGGACCTCAGCCCTG	18803
rs27303567	snp	A/G	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160756237	GCTCCACAGGGCTGT[A/G]CACTTACTCTTACTG	18803
rs27303568	snp	C/T	0.231111	0.249285	intron-variant	Plcg1	Mm_Celera	2:160756164	TTAGGGTCTTCTTGG[C/T]TTTGACCTTTTCTTT	18803
rs27303569	snp	G/T	0.231111	0.249285	intron-variant	Plcg1	Mm_Celera	2:160756126	TGGCACACTGTCCAG[G/T]CATTCCCTTCGTTAT	18803
rs27303570	snp	A/G	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160756099	TGGGTAGTAAGTAGA[A/G]CAGGGGCCAGATGGC	18803
rs27303571	snp	C/T	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160756073	CTTCAGAGTGATCCC[C/T]GTGTCTTCCATGGGT	18803
rs27303572	snp	C/T	0.32	0.24	intron-variant	Plcg1	Mm_Celera	2:160755293	TGCAAGGGTCTTGGA[C/T]CAGTGTTGTGGTTTT	18803
rs27303573	snp	C/T	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160754751	TGCTGACTGTCCTGT[C/T]ATTGTGAAGGGCTGA	18803
rs27303574	snp	C/T	0.32	0.24	synonymous-codon	Plcg1	Mm_Celera	2:160754653	GGTGCGGAAACGCAA[C/T]GAGCCTAACTCATAT	18803
rs27303575	snp	C/T	0.124444	0.216185	synonymous-codon	Plcg1	Mm_Celera	2:160754572	TTTCAGGTGGTACCA[C/T]GCAAGCCTGACTAGA	18803
rs27303576	snp	A/G	0.124444	0.216185	missense	Plcg1	Mm_Celera	2:160753932	CTCACTGAGTACTGC[A/G]TAGAGACTGGGGCTC	18803
rs27303577	snp	C/T	0.124444	0.216185	synonymous-codon	Plcg1	Mm_Celera	2:160753865	GAGTGAGAAGTGGTT[C/T]CACGGGAAGCTCGGG	18803
rs27303578	snp	C/T	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160753811	TGGGTATCTTTGCTG[C/T]CATCCTGTCTAGGCC	18803
rs27303579	snp	A/C	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160753788	CTGAATGAGAACGTG[A/C]CAGTCACTGGGTATC	18803
rs27303580	snp	A/G	0.32	0.24	intron-variant	Plcg1	Mm_Celera	2:160753359	CCTTATTAAGGTGTG[A/G]CATCGTTGCCAGGAG	18803
rs27303581	snp	G/T	0.231111	0.249285	intron-variant	Plcg1	Mm_Celera	2:160753174	TTACTGTCCTGGCCC[G/T]TTGCCTTCAGGTACC	18803
rs27303582	snp	A/G	0.132653	0.220748	intron-variant	Plcg1	Mm_Celera	2:160752885	GCACTGAAAGGATCC[A/G]CAAGCTGCACTGGGG	18803
rs27303583	snp	C/T	0.32	0.24	intron-variant	Plcg1	Mm_Celera	2:160752223	TGAGTAAGCCTCTTT[C/T]TGCTCATCCAACCCT	18803
rs27303584	snp	A/G	0.188366	0.242283	missense	Plcg1	Mm_Celera	2:160751644	ACAGGACTGGAGAGC[A/G]TCCGGAGCATTGCCA	18803
rs27303585	snp	A/T	0.32	0.24	intron-variant	Plcg1	Mm_Celera	2:160751595	TAGACGGGGGCCCTT[A/T]GTCAGCCAGTGCCAG	18803
rs27303586	snp	C/T	0.42	0.183303	intron-variant	Plcg1	Mm_Celera	2:160751309	CCTGCTTTGGAGTGG[C/T]TTTGGTGCCATTACT	18803
rs27303587	snp	C/T	0.244898	0.249948	intron-variant	Plcg1	Mm_Celera	2:160751124	GGCTTGACTGGCAGT[C/T]TTGCTCTGTACTATG	18803
rs27303588	snp	C/T	0.345679	0.230967	intron-variant	Plcg1	Mm_Celera	2:160751112	CTCCTCCTAAGGGGC[C/T]TGACTGGCAGTTTTG	18803
rs27303589	snp	A/T	0.231111	0.249285	intron-variant	Plcg1	Mm_Celera	2:160750536	TTTTCCTGGAGCCTC[A/T]GGAGTGTGCTCAGCA	18803
rs27303590	snp	C/T	0.498615	0.0262793	intron-variant	Plcg1	Mm_Celera	2:160750514	TTCTGTCCCTCTCTC[C/T]GAGTTCTTTTCCTGG	18803
rs27303591	snp	C/T	0.32	0.24	intron-variant	Plcg1	Mm_Celera	2:160750429	TCCAAGCTGCTATGC[C/T]TAGAGGGTAGAGTGC	18803
rs27303592	snp	C/T	0.231111	0.249285	intron-variant	Plcg1	Mm_Celera	2:160749929	GGGTGGAGAGAGCAG[C/T]GTGATTTTTATGACA	18803
rs27303593	snp	A/C	0.142012	0.225474	intron-variant	Plcg1	Mm_Celera	2:160749577	TAGGAAAGGAGGAGT[A/C]TGCTTAACCCTTCTG	18803
rs27303594	snp	C/T	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160749203	TTTGGGCTATGTTCT[C/T]TGTTTAAAATTGCAT	18803
rs27303595	snp	C/T	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160749125	CTGTTAGACACTGTC[C/T]GACCATTCTGGGTGT	18803
rs27303596	snp	C/T	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160749095	ACACAACCAAGATCA[C/T]ACTGCTGTAGAGGGC	18803
rs27303597	snp	A/G	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160748644	CCTGCTCTGACCTAG[A/G]GTTTCCCCAGTGTCC	18803
rs27303598	snp	C/G	0.231111	0.249285	intron-variant	Plcg1	Mm_Celera	2:160748612	GGCAGGAAGCCATGG[C/G]ATGTGTAGAGGAGTG	18803
rs27303599	snp	A/G	0.231111	0.249285	intron-variant	Plcg1	Mm_Celera	2:160748501	TGGACTTCTAGGTGT[A/G]ACTGGCAATGCAGCC	18803
rs27303600	snp	A/T	0.197531	0.244432	intron-variant	Plcg1	Mm_Celera	2:160748143	GTAAGAATCGTCTTC[A/T]TGTGGTTAAAACTGT	18803
rs27303601	snp	A/G	0.231111	0.249285	intron-variant	Plcg1	Mm_Celera	2:160748018	GCCCTTGGTTCAGCC[A/G]CTGCTCTGCTCACAG	18803
rs27303602	snp	A/G	0.231111	0.249285	synonymous-codon	Plcg1	Mm_Celera	2:160747893	TGTCATCCTCTATGG[A/G]ATGGAATTCCGCTTG	18803
rs27303603	snp	A/G	0.197531	0.244432	synonymous-codon	Plcg1	Mm_Celera	2:160747866	CTTCCGGCCAGATCA[A/G]TCACACTGCTTTGTC	18803
rs27303604	snp	A/G	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160747688	GAGGAAGGAGGGTGT[A/G]GAAGTGAGTGAGGAG	18803
rs27303605	snp	A/G	0.132653	0.220748	intron-variant	Plcg1	Mm_Celera	2:160747683	GCCCTGAGGAAGGAG[A/G]GTGTGGAAGTGAGTG	18803
rs27303606	snp	G/T	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160747644	GTTCGGTCTGTGTCA[G/T]AAAGGGTTGCTCTTT	18803
rs27303607	snp	C/T	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160747427	GACCCTGCTCTTTTC[C/T]GGGTCTGAGTGTGTA	18803
rs27303608	snp	G/T	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160747369	AGCTGGGTCTGCGTA[G/T]GTATTGTGTTAGAAA	18803
rs27303609	snp	G/T	0.42	0.183303	intron-variant	Plcg1	Mm_Celera	2:160747157	TTGTAACTGAGATAA[G/T]GATACCAAGCTGCAC	18803
rs27303610	snp	A/G	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160747095	CTCAGGCTCGTGTAC[A/G]TGCCTCACCTTGGCT	18803
rs27303611	snp	A/G	0.231111	0.249285	intron-variant	Plcg1	Mm_Celera	2:160747018	CTTTAGTGGTCACTC[A/G]CTAACAGTTGCTCTG	18803
rs27303612	snp	C/T	0.244898	0.249948	intron-variant	Plcg1	Mm_Celera	2:160746784	CTGGCTAAGGAACAG[C/T]CCCCTTTTTGTGGGG	18803
rs27303613	snp	A/G	0.231111	0.249285	intron-variant	Plcg1	Mm_Celera	2:160745420	ATACACACCATCCAT[A/G]TGTGCACGTATATAT	18803
rs27303614	snp	A/C	0.244898	0.249948	intron-variant	Plcg1	Mm_Celera	2:160745161	CTGTCAGGTCCTTCT[A/C]GTCTGCTTCTGACTT	18803
rs27303615	snp	A/G	0.132653	0.220748	intron-variant	Plcg1	Mm_Celera	2:160745085	TAGGAATGAGCCTGG[A/G]CTCTCTGTTTGTCCT	18803
rs27303616	snp	C/T	0.231111	0.249285	intron-variant	Plcg1	Mm_Celera	2:160745055	AGGTAGTCTCTTCCC[C/T]GTGGTGGCAGTTTCT	18803
rs27303617	snp	A/G	0.124444	0.216185	intron-variant	Plcg1	Mm_Celera	2:160744954	ACACAGTCATTCCTG[A/G]CATACAGAAGGTCTC	18803

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