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
rs6206809	snp	A/C	0.48	0.0979796	intron-variant	Pcgf6	Mm_Celera	19:47045201	CTTGAGAAGAAAAGT[A/C]ACGACTTTAAAGCTA	71041
rs6207258	snp	A/G	0.5	0	intron-variant	Pcgf6	GRCm38.p3	19:47045257	AAAACaaataattca[A/G]cagttaaaagtactt	71041
rs6207896	snp	C/T	0.5	0	intron-variant	Pcgf6	Mm_Celera	19:47045400	catttacatcgtaca[C/T]gcttataacatacat	71041
rs30317981	snp	A/G	0.444444	0.157135	upstream-variant-2KB	Pcgf6	GRCm38.p3	19:47052803	CCACTTCTGGTCCTG[A/G]ACTGAGCTCTCTGCT	71041
rs30318013	snp	C/T	0.375	0.216506	intron-variant	Pcgf6	GRCm38.p3	19:47046500	CCACAGGTCCTGACT[C/T]CAATTCCCAGCTCAA	71041
rs30363113	snp	C/T	0.444444	0.157135	intron-variant	Pcgf6	Mm_Celera	19:47050129	GGGGTCCCAAACCCT[C/T]TCAACATCCTGCAGA	71041
rs30363910	snp	C/T	0.5	0	intron-variant	Pcgf6	GRCm38.p3	19:47035686	CTGTGAGTTCAAGAC[C/T]AGCCTGGTCTACAGA	71041
rs30365659	snp	C/T	0.5	0	intron-variant	Pcgf6	GRCm38.p3	19:47046853	GATGAAACAATCTGC[C/T]TAAGGTCACAAAGTA	71041
rs30407812	snp	C/T	0.5	0	intron-variant	Pcgf6	GRCm38.p3	19:47041780	TGGTGGTGGCCAACA[C/T]CTTTAATCCCAGCAC	71041
rs30407954	snp	A/G	0.5	0	upstream-variant-2KB	Pcgf6	GRCm38.p3	19:47051149	CTCTAGATGCCATGT[A/G]TTCTTGAATTAGGAG	71041
rs30414237	snp	A/C/T	0.497041	0.0383476	upstream-variant-2KB	Pcgf6	GRCm38.p3	19:47052848	ACACATGAAGACTTA[A/C/T]GGCTCAAACTCCTGG	71041
rs30519778	snp	C/G	0.5	0	downstream-variant-500B	Pcgf6	Mm_Celera	19:47033245	CCTGCAGGCCCTGCT[C/G]GTCACTCCCTGAACC	71041
rs30670880	snp	A/G/T	0.444444	0.157135	intron-variant	Pcgf6	GRCm38.p3	19:47037398	GGGCAGCGGTGGCAC[A/G/T]CGCCTTTAATCCCAG	71041
rs30752496	snp	A/G	0.5	0	intron-variant	Pcgf6	GRCm38.p3	19:47048437	GCCCCAAGTACACAT[A/G]TGGTACACATGCACA	71041
rs30759107	snp	C/T	0.48	0.0979796	intron-variant	Pcgf6	GRCm38.p3	19:47046541	TAAGAGATCTGGTGC[C/T]CTCTTTTGGCATGCA	71041
rs30812470	snp	C/T	0.444444	0.157135	intron-variant	Pcgf6	Mm_Celera	19:47040893	CAAGAATGCTCTGGG[C/T]TCTGCCTGCTGAGCA	71041
rs30852407	snp	C/T	0.465374	0.126941	intron-variant	Pcgf6	GRCm38.p3	19:47048608	TCCAGCAGATCTAGC[C/T]GTCTGTGCCTGATAC	71041
rs30902318	snp	A/C	0.444444	0.157135	upstream-variant-2KB	Pcgf6	GRCm38.p3	19:47052971	CTCTTGTCTCTAACA[A/C]GCCAAATGACAAAAG	71041
rs30937916	snp	A/G	0.5	0	intron-variant	Pcgf6	GRCm38.p3	19:47043236	GCAGCACGTACACAG[A/G]TTTGAAATGAAGTTT	71041
rs31005739	snp	A/C	0.459184	0.136902	intron-variant, downstream-variant-500B	Pcgf6	GRCm38.p3	19:47037152	GGCAGCACTCCTAAT[A/C]CCTGAGCCATATCTT	71041
rs31045283	snp	A/C	0.5	0	intron-variant	Pcgf6	GRCm38.p3	19:47035629	AGAAAATGGGCACAC[A/C]ACTTTTATTTCAGCA	71041
rs31183928	snp	A/C	0.375	0.216506	intron-variant	Pcgf6	Mm_Celera	19:47046359	TGTCGAGAACCCCCC[A/C]CACACACACACACAA	71041
rs31207973	snp	G/T	0.5	0	upstream-variant-2KB	Pcgf6	GRCm38.p3	19:47051431	TAAGCCAAGTATGGT[G/T]ACCTACTTATTAATT	71041
rs31236067	snp	A/G	0.493827	0.0552116	intron-variant	Pcgf6	Mm_Celera	19:47042824	AAGTTAATCAAAACA[A/G]TATTTTAAATTACAT	71041
rs36274604	snp	A/T	0.396694	0.202437	intron-variant	Pcgf6	Mm_Celera	19:47046153	TCTCTCTCCTAGGCC[A/T]CACGTGGCAAGGAGA	71041
rs36275961	snp	A/T	0.231111	0.249285	intron-variant	Pcgf6	Mm_Celera	19:47049203	TACACAAGTCAGCTG[A/T]GACATCTGAGCCCAA	71041
rs36303163	snp	C/T	0.244898	0.249948	intron-variant	Pcgf6	Mm_Celera	19:47039246	AATAACATGCAAGGT[C/T]TGACGTTTTCTAATT	71041
rs36315339	snp	A/C/G	0.231111	0.249285	utr-variant-3-prime, nc-transcript-variant	Pcgf6	GRCm38.p3	19:47034172	TTTGAAGTTCAGAAT[A/C/G]GGACAGGAACTTGTA	71041
rs36324771	snp	C/T	0.5	0	upstream-variant-2KB	Pcgf6	Mm_Celera	19:47051108	TCAGTATTTTACTTG[C/T]ACCAGTTTATTCATG	71041
rs36331276	snp	A/T	0.124444	0.216185	downstream-variant-500B	Pcgf6	Mm_Celera	19:47033289	GAGTTAGTTATCATC[A/T]GTGAAAGAGAAGCTG	71041
rs36340644	snp	A/G	0.165289	0.235211	synonymous-codon, nc-transcript-variant, missense	Pcgf6	Mm_Celera	19:47042778	TACCTTAAAATGTCC[A/G]GTGTCTTCATTAGCA	71041
rs36341351	snp	A/G	0.152778	0.230321	synonymous-codon, nc-transcript-variant, utr-variant-3-prime	Pcgf6	GRCm38.p3	19:47040062	ACAAGCTGGATCAAG[A/G]CCCATTTTTCTTCTA	71041
rs36346155	snp	A/T	0.142012	0.225474	intron-variant	Pcgf6	Mm_Celera	19:47038506	TTGGTAATCTTTACC[A/T]TTATTCCAGTATTTT	71041
rs36365082	snp	A/G	0.142012	0.225474	intron-variant	Pcgf6	Mm_Celera	19:47042004	AAACGAAACAACCCT[A/G]ACCTTTCCTTAATAA	71041
rs36371102	snp	C/T	0.497778	0.0332592	intron-variant	Pcgf6	GRCm38.p3	19:47046175	GCAAGGAGAGGGAGT[C/T]CTGCCAAGTGGATAC	71041
rs36389887	snp	A/G	0.5	0	upstream-variant-2KB	Pcgf6	Mm_Celera	19:47051468	TTGAGTAGGCAGAAT[A/G]TTAGAGCCAAGGAAT	71041
rs36416970	snp	C/T	0.132653	0.220748	utr-variant-3-prime, nc-transcript-variant	Pcgf6	Mm_Celera	19:47034496	CACACAATGCTAGGG[C/T]TCTGGTGACAACAGA	71041
rs36420388	snp	C/T	0.165289	0.235211	intron-variant	Pcgf6	Mm_Celera	19:47041666	GTATTGCATCAACCA[C/T]TCATCTCTCTAAATG	71041
rs36434407	snp	A/G	0.132653	0.220748	downstream-variant-500B	Pcgf6	Mm_Celera	19:47033381	GAGTGTGACAACACC[A/G]GATAAATGCCTATTC	71041
rs36509129	snp	A/G	0.152778	0.230321	intron-variant	Pcgf6	Mm_Celera	19:47036707	GGAAGGTAATTAGAT[A/G]AAGGATCTCTACTCC	71041
rs36562722	snp	A/C	0.336735	0.234472	utr-variant-3-prime, nc-transcript-variant	Pcgf6	GRCm38.p3	19:47034433	TTATGAGTGCTGTTT[A/C]CATAGTCTTTAGTGT	71041
rs36607151	snp	A/G	0.336735	0.234472	intron-variant	Pcgf6	Mm_Celera	19:47034698	GTCCTGAAGAGGGGA[A/G]AAGGATATTTTATAG	71041
rs36624720	snp	C/T	0.132653	0.220748	intron-variant	Pcgf6	Mm_Celera	19:47044799	GCACAAGCTGCATTC[C/T]GGGACACTCTTGGGC	71041
rs36711363	snp	A/T	0.165289	0.235211	intron-variant	Pcgf6	Mm_Celera	19:47036670	ATTCCTAGTATAGAG[A/T]ACTAAAGATATGGGG	71041
rs36739023	snp	C/T	0.391111	0.206368	utr-variant-3-prime, nc-transcript-variant	Pcgf6	GRCm38.p3	19:47033888	ACAGAAACATTAACA[C/T]GGAACCAGATCATTT	71041
rs36770384	snp	C/G	0.32	0.24	intron-variant, downstream-variant-500B	Pcgf6	Mm_Celera	19:47047839	ACTAAACCTCTTCTA[C/G]CCCGAGTGGCCTCCA	71041
rs36786861	snp	C/T	0.142012	0.225474	intron-variant	Pcgf6	Mm_Celera	19:47038053	CCAGTCTAAGCTGCA[C/T]ACTGAGACCTTAACT	71041
rs36793772	snp	A/G	0.444444	0.157135	intron-variant	Pcgf6	GRCm38.p3	19:47046157	TCTCCTAGGCCACAC[A/G]TGGCAAGGAGAGGGA	71041
rs36833042	snp	C/T	0.152778	0.230321	intron-variant	Pcgf6	Mm_Celera	19:47042181	AACTTCAGCCAAAAA[C/T]GTTAAATATACAAGT	71041
rs36862493	snp	A/G	0.444444	0.157135	intron-variant	Pcgf6	GRCm38.p3	19:47045776	CTTTGAAATTCCAAA[A/G]ATAAGCAAATGGTAA	71041
rs36887446	snp	A/T	0.244898	0.249948	intron-variant	Pcgf6	Mm_Celera	19:47038066	CATACTGAGACCTTA[A/T]CTAACAGCCAGCCAG	71041
rs36895593	snp	A/G	0.336735	0.234472	downstream-variant-500B	Pcgf6	Mm_Celera	19:47033319	GATGGCGAACTCTGC[A/G]GTTACCCACTGTCGG	71041
rs36922454	snp	G/T	0.32	0.24	intron-variant	Pcgf6	Mm_Celera	19:47048291	AGAACGTGAACTTGA[G/T]GCCGGACTGCATTTT	71041
rs36934944	snp	C/T	0.132653	0.220748	utr-variant-3-prime, nc-transcript-variant	Pcgf6	Mm_Celera	19:47034229	GCACCCGAGGTTTAA[C/T]AGACTGGCTCTGAAC	71041
rs36941662	snp	A/G	0.231111	0.249285	intron-variant	Pcgf6	Mm_Celera	19:47048967	TTTAAAACACCATTC[A/G]GAAATGCGAACTATG	71041
rs36966412	snp	A/G	0.493827	0.0552116	intron-variant	Pcgf6	Mm_Celera	19:47044068	AATCTTTGGGGAGTG[A/G]CTACTAAAGCTGAGG	71041
rs36968460	snp	A/T	0.35503	0.226867	utr-variant-3-prime, nc-transcript-variant	Pcgf6	Mm_Celera	19:47034109	ACAGGAGACAGTCTC[A/T]GCCTCAGAGCTGAGG	71041
rs37007136	snp	A/G	0.244898	0.249948	synonymous-codon, nc-transcript-variant	Pcgf6	GRCm38.p3	19:47049072	GTAGGGGGTCAGCTC[A/G]ACAAGGTTTATCAGG	71041
rs37008235	snp	C/T	0.336735	0.234472	intron-variant	Pcgf6	Mm_Celera	19:47035203	TTAAGTGGTCAAGAA[C/T]TTCTGAACTGAAACA	71041
rs37013672	snp	A/T	0.32	0.24	intron-variant	Pcgf6	Mm_Celera	19:47035452	GATCTGTTCAAGAAA[A/T]AAAATGCTGGGATGG	71041
rs37039121	snp	A/G	0.297521	0.245442	intron-variant	Pcgf6	Mm_Celera	19:47040883	GTGGTGCTGGCAAGA[A/G]TGCTCTGGGTTCTGC	71041
rs37054592	snp	C/T	0.132653	0.220748	utr-variant-3-prime, nc-transcript-variant	Pcgf6	Mm_Celera	19:47034272	TGTTCTGAAGGAAAC[C/T]ACCCAGCCCATGCAG	71041
rs37067668	snp	A/G	0.152778	0.230321	intron-variant	Pcgf6	Mm_Celera	19:47040989	TCCAGTAAAAGGGCA[A/G]TCGCCTTAGATTTCT	71041
rs37112616	snp	A/G	0.244898	0.249948	intron-variant, downstream-variant-500B	Pcgf6	Mm_Celera	19:47037132	ATAGGTTCTCTGTGC[A/G]AACAGGCAGCACTCC	71041
rs37149729	snp	C/T	0.244898	0.249948	intron-variant	Pcgf6	Mm_Celera	19:47036149	TTTTGTATTTCCCTG[C/T]CATAGTTCAGAAATG	71041
rs37166577	snp	C/G	0.231111	0.249285	downstream-variant-500B	Pcgf6	Mm_Celera	19:47033356	CCGCAGAGCAGAGCA[C/G]AGCATCAGTGAGTGT	71041
rs37173032	snp	A/G	0.277778	0.248452	intron-variant	Pcgf6	Mm_Celera	19:47041690	CTAAATGTCACACTA[A/G]GGTGGGCAGCTGAGC	71041
rs37183784	snp	C/T	0.473373	0.11227	intron-variant	Pcgf6	GRCm38.p3	19:47044231	GCAGGGCCTTGATAT[C/T]CAGCTGAGGCTAGCT	71041
rs37191463	snp	A/T	0.165289	0.235211	intron-variant	Pcgf6	Mm_Celera	19:47034949	AAGACAGAATCTTCC[A/T]GTAAGGCCCAGGCTG	71041
rs37219555	snp	C/T	0.152778	0.230321	intron-variant	Pcgf6	Mm_Celera	19:47048761	CACTGGCAACAATGA[C/T]TTTAAATGTGGATAC	71041
rs37284974	snp	G/T	0.197531	0.244432	intron-variant	Pcgf6	Mm_Celera	19:47036598	ATATCTCTATTATAG[G/T]CCTATATGATGGTTA	71041
rs37302488	snp	G/T	0.486111	0.0821678	intron-variant	Pcgf6	GRCm38.p3	19:47039308	CAAAAGAACTGGAAT[G/T]TAGGCCTAGAAACCT	71041
rs37331100	snp	C/T	0.132653	0.220748	intron-variant	Pcgf6	Mm_Celera	19:47039992	CACTCTTTCTCCATC[C/T]GTCAAAGGTCATCCT	71041
rs37408038	snp	A/G	0.486111	0.0821678	intron-variant	Pcgf6	GRCm38.p3	19:47043934	GGCTTGGAACTAAAA[A/G]AAAGCGCCACCATGC	71041
rs37430409	snp	C/G	0.142012	0.225474	intron-variant	Pcgf6	Mm_Celera	19:47039933	CTGAATTAACAGTCT[C/G]AGTCATCTACATCAT	71041
rs37467723	snp	A/T	0.244898	0.249948	intron-variant	Pcgf6	Mm_Celera	19:47049788	CCTTCAAAATATCCA[A/T]TCTAAAGAAAACACT	71041
rs37481022	snp	A/G	0.32	0.24	intron-variant, downstream-variant-500B	Pcgf6	Mm_Celera	19:47047903	CAGCACCTCAACAAC[A/G]GTTTGTTCTTTAATC	71041
rs37489603	snp	A/G	0.46281	0.131194	intron-variant	Pcgf6	GRCm38.p3	19:47044669	TGTGTGTGCTACTGT[A/G]GGATACGGATCCCAG	71041
rs37502789	snp	C/T	0.165289	0.235211	intron-variant	Pcgf6	Mm_Celera	19:47038374	ATGAGCTCAATAGCA[C/T]TGCCTAGCAAATATG	71041
rs37516938	snp	A/G	0.336735	0.234472	synonymous-codon, nc-transcript-variant, missense	Pcgf6	GRCm38.p3	19:47040098	TTTTTCTACATGCCC[A/G]ATAGTTGCTTCTCCT	71041
rs37529265	snp	A/T	0.231111	0.249285	intron-variant	Pcgf6	Mm_Celera	19:47049191	TATATTCCAACTTAC[A/T]CAAGTCAGCTGTGAC	71041
rs37529970	snp	A/T	0.260355	0.249785	intron-variant	Pcgf6	Mm_Celera	19:47042721	ATCTGATTCAGAATT[A/T]ATACCTACAGAATCC	71041
rs37537140	snp	C/T	0.142012	0.225474	intron-variant	Pcgf6	Mm_Celera	19:47036459	GATCTCGAAATTACT[C/T]CAGTGCACACATAAG	71041
rs37554185	snp	A/G	0.260355	0.249785	downstream-variant-500B	Pcgf6	Mm_Celera	19:47033375	ATCAGTGAGTGTGAC[A/G]ACACCGGATAAATGC	71041
rs37629828	snp	G/T	0.124444	0.216185	intron-variant, downstream-variant-500B	Pcgf6	Mm_Celera	19:47047753	CAGGCAGCAAGTGCC[G/T]TCTCTTGGTACTGGT	71041
rs37690916	snp	G/T	0.260355	0.249785	utr-variant-3-prime, nc-transcript-variant	Pcgf6	GRCm38.p3	19:47034001	CATTCACAGCCACAC[G/T]GAGGGAATTTTGTGA	71041
rs37704344	snp	C/T	0.260355	0.249785	intron-variant	Pcgf6	Mm_Celera	19:47049700	GCCAACACTACAAGG[C/T]CTCATTTCAAAACAA	71041
rs37797194	snp	C/T	0.124444	0.216185	downstream-variant-500B	Pcgf6	Mm_Celera	19:47033120	TCCCTGCATGACAAC[C/T]GGAATAAGACAACCA	71041
rs37878162	snp	A/G	0.142012	0.225474	intron-variant	Pcgf6	Mm_Celera	19:47040330	TTGTAATAGAAAGGC[A/G]TGTTAGTTAACTTTA	71041
rs37898367	snp	A/G	0.260355	0.249785	intron-variant	Pcgf6	Mm_Celera	19:47049899	CCCTTAAACCTGCCT[A/G]GTCTCCCCACATTAC	71041
rs37913140	snp	C/T	0.165289	0.235211	intron-variant	Pcgf6	Mm_Celera	19:47044058	ACTGCAAAGGAATCT[C/T]TGGGGAGTGACTACT	71041
rs37984911	snp	A/G	0.35503	0.226867	utr-variant-3-prime, nc-transcript-variant	Pcgf6	GRCm38.p3	19:47034063	ACCTCATATTTGTTT[A/G]AGGGATGTTAGTTAA	71041
rs38036821	snp	A/G	0.132653	0.220748	utr-variant-3-prime, nc-transcript-variant	Pcgf6	Mm_Celera	19:47034452	AGTCTTTAGTGTAGC[A/G]AATACATTCTATTGT	71041
rs38115606	snp	A/G	0.142012	0.225474	intron-variant	Pcgf6	Mm_Celera	19:47038455	TCTAGGATCTGGAAC[A/G]CTTAAACAAAGACAC	71041
rs38125682	snp	C/G	0.142012	0.225474	intron-variant	Pcgf6	Mm_Celera	19:47042006	ACGAAACAACCCTGA[C/G]CTTTCCTTAATAAAA	71041
rs38143286	snp	A/T	0.336735	0.234472	intron-variant	Pcgf6	Mm_Celera	19:47035296	GTGTGTTGACTCTCA[A/T]ATAAGCATAGGTAAC	71041
rs38144428	snp	C/T	0.426035	0.177515	intron-variant	Pcgf6	Mm_Celera	19:47046134	GTGCTTGTTACCAAG[C/T]GAGTCTCTCTCCTAG	71041
rs38158598	snp	C/T	0.336735	0.234472	downstream-variant-500B	Pcgf6	Mm_Celera	19:47033182	CTCCCTCTGCTGAGC[C/T]TTCATTGGCATCCTC	71041
rs38214835	snp	C/T	0.277778	0.248452	intron-variant	Pcgf6	Mm_Celera	19:47042532	AAAATTACCAATCAA[C/T]GGGGCATGTGGCTTT	71041
rs38236562	snp	C/T	0.473373	0.11227	intron-variant	Pcgf6	Mm_Celera	19:47044125	AAGGCTTCTGCTGCA[C/T]TAATAGTGGTTTTGT	71041

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