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
rs6307298	snp	C/T	0.456747	0.140554	intron-variant	Nsmce1	GRCm38.p3	7:125478175	GCTCTGTGCCACCAG[C/T]GCAGCAGGAGAGGCC	67711
rs6307345	snp	C/G	0.415225	0.187619	intron-variant	Nsmce1	GRCm38.p3	7:125478203	GCCCAGCTGAAACCA[C/G]AGCGCCTCACCTTGC	67711
rs6321026	snp	A/G	0.49827	0.0293608	intron-variant	Nsmce1	Mm_Celera	7:125478449	CCACTATAGGGCACC[A/G]CATACCACAGGGCTC	67711
rs13463793	snp	C/T			synonymous-codon	Nsmce1	GRCm38.p3	7:125469035	CTGCCACGGCCTCCT[C/T]ATCCAGGTACTGCAG	67711
rs13463794	snp	C/T	0.444444	0.157135	synonymous-codon	Nsmce1	GRCm38.p3	7:125471253	CTCTTGCAGCTGGAA[C/T]TGATCGTTGACTCAG	67711
rs13463796	snp	C/T			missense	Nsmce1	Mm_Celera	7:125486412	GGCGCTTCCTCCAGC[C/T]GCTCATGACCCACGG	67711
rs31392387	snp	C/G	0.188366	0.242283	intron-variant, upstream-variant-2KB	Nsmce1	Mm_Celera	7:125487815	AACTACCTACCATGC[C/G]TGTCTCAGATGTTTC	67711
rs31423805	snp	A/T	0.32	0.24	upstream-variant-2KB	Nsmce1	Mm_Celera	7:125492004	GCATAAGAGACGATC[A/T]CACACACACACACAC	67711
rs31648559	snp	A/G	0.498615	0.0262793	intron-variant	Nsmce1	GRCm38.p3	7:125481509	CTTAAAGAATGTTGT[A/G]TGTGAGAGACTGAGT	67711
rs31790313	snp	A/G	0.375	0.216506	intron-variant	Nsmce1	Mm_Celera	7:125475632	GTGAGCAGGCTCTGG[A/G]CTGACCCCGGGGCTG	67711
rs32135114	snp	G/T	0.459184	0.136902	intron-variant	Nsmce1	GRCm38.p3	7:125480569	GAGTTAACTTTCTTT[G/T]CCTCTATCATGTATC	67711
rs32356264	snp	A/G	0.18	0.24	intron-variant	Nsmce1	Mm_Celera	7:125485006	AAGCTTCAGTAGGCC[A/G]CCCTGCTCAAGGCCT	67711
rs32986684	snp	C/T	0.124444	0.216185	downstream-variant-500B	Nsmce1	Mm_Celera	7:125467550	ACGAAGCAATGGCAC[C/T]CAGAGCCAGCCAAAG	67711
rs32986687	snp	A/G	0.132653	0.220748	downstream-variant-500B	Nsmce1	Mm_Celera	7:125467562	CACCCAGAGCCAGCC[A/G]AAGAGACATCTGCCC	67711
rs32986690	snp	A/G	0.277778	0.248452	utr-variant-3-prime	Nsmce1	GRCm38.p3	7:125467714	AACAAAGGAGGCACG[A/G]CAGTCCTAAATGGAC	67711
rs32986693	snp	C/G	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125467865	ATAGAACAGCACAGA[C/G]ACACACAATGAGCAG	67711
rs32986954	snp	A/G	0.497778	0.0332592	intron-variant	Nsmce1	GRCm38.p3	7:125470072	TCCCGGGTCCATACT[A/G]GTGGCCAGCTTCCTG	67711
rs32986957	snp	C/T	0.489796	0.070696	intron-variant	Nsmce1	GRCm38.p3	7:125470083	TACTAGTGGCCAGCT[C/T]CCTGAACCTCCTTCT	67711
rs32986960	snp	C/T	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125470212	AGCCTCCTAGTGGAC[C/T]ATCCAGCTGCATAAT	67711
rs32986963	snp	A/G	0.497778	0.0332592	intron-variant	Nsmce1	GRCm38.p3	7:125470278	CCTTAGCAAAGGGAG[A/G]CTGCATTTCTGAGGC	67711
rs32987266	snp	C/T	0.48	0.0979796	intron-variant	Nsmce1	GRCm38.p3	7:125472916	CAAAGGGAGAGGGCA[C/T]GTGTTACACATCCCA	67711
rs32987269	snp	G/T	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125472985	CTCTAACACAGTGAA[G/T]GCATACGGCCAGCTT	67711
rs32987272	snp	C/T	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125473063	GTATACCTGTTTTCA[C/T]TTATTAAAATAATGT	67711
rs32987485	snp	A/C	0.391111	0.206368	intron-variant	Nsmce1	GRCm38.p3	7:125467893	CAGCAGGACCAATGG[A/C]CTGATCACACAGTAC	67711
rs32987486	snp	A/G	0.408163	0.193609	intron-variant	Nsmce1	GRCm38.p3	7:125468042	CATCCCTGTCCCTGG[A/G]TGGCTATAAGGACAG	67711
rs32987489	snp	C/T	0.459184	0.136902	intron-variant	Nsmce1	GRCm38.p3	7:125468156	GGTCACTAACGATGA[C/T]CTTCATGCTCAGAGA	67711
rs32987492	snp	C/T	0.459184	0.136902	intron-variant	Nsmce1	GRCm38.p3	7:125468433	ATGACCATGGACAAG[C/T]ACATCTCTCAACTTC	67711
rs32987726	snp	A/G	0.444444	0.157135	intron-variant	Nsmce1	GRCm38.p3	7:125470336	CGGATCAAGGAACCA[A/G]ATGCCTAGGAAGGCT	67711
rs32987728	snp	C/T	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125470455	CCCAGAGGTGCTCTC[C/T]CAACCGCGACCCCTA	67711
rs32987731	snp	A/C/T	0.426035	0.177515	intron-variant	Nsmce1	Mm_Celera	7:125470486	CTGCCTGAGCCTGTG[A/C/T]CTTCCTTCACCAGAT	67711
rs32987985	snp	C/T	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125473373	AAACAGACACCATGC[C/T]ACCATTTATGTTACT	67711
rs32987987	snp	C/T	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125473425	AGAAAGAAGACTCAT[C/T]TAAAGGGTCAGTCTC	67711
rs32987990	snp	A/C	0.132653	0.220748	intron-variant	Nsmce1	Mm_Celera	7:125473428	AAGAAGACTCATCTA[A/C]AGGGTCAGTCTCACT	67711
rs32987993	snp	C/G	0.48	0.0979796	intron-variant	Nsmce1	GRCm38.p3	7:125473650	AGTTAAATGAAAAAT[C/G]AGTATCAGCTATTAA	67711
rs32988315	snp	C/T	0.489796	0.070696	intron-variant	Nsmce1	Mm_Celera	7:125468505	GAGGGTTTAACCTTC[C/T]AGGCCCCAACTTAAT	67711
rs32988318	snp	A/G	0.231111	0.249285	intron-variant	Nsmce1	Mm_Celera	7:125468566	GAGTCCCTGGTGGGA[A/G]ATAGAGGCATACAGT	67711
rs32988321	snp	A/C	0.32	0.24	intron-variant	Nsmce1	Mm_Celera	7:125468593	CAGTTTTGTAGTAGG[A/C]CAAGTAGCAACATGT	67711
rs32988323	snp	A/C	0.489796	0.070696	intron-variant	Nsmce1	GRCm38.p3	7:125468622	GTATCGCACACTTTA[A/C]GATCAAGAGAAGCAT	67711
rs32988324	snp	C/T	0.444444	0.157135	intron-variant	Nsmce1	Mm_Celera	7:125470626	AGATTTTTTTCAGGA[C/T]TCCCATTAAACCCTT	67711
rs32988327	snp	C/T	0.32	0.24	intron-variant	Nsmce1	GRCm38.p3	7:125471000	GGGAACACAGGCTCT[C/T]CTCTCAGAGGTCATG	67711
rs32988330	snp	C/T	0.48	0.0979796	intron-variant	Nsmce1	GRCm38.p3	7:125471014	TCCTCTCAGAGGTCA[C/T]GGAAAGCTTACAATA	67711
rs32988333	snp	A/G	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125471053	CCCACAGACAGGCCG[A/G]GCTCAACTGCTAGCA	67711
rs32988686	snp	A/C	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125473673	GCTATTAAGTGGAAA[A/C]CAATGATGCGGGAGG	67711
rs32988689	snp	G/T	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125473683	GGAAAACAATGATGC[G/T]GGAGGAGGAAGCCAG	67711
rs32988692	snp	A/T	0.497778	0.0332592	intron-variant	Nsmce1	GRCm38.p3	7:125473780	TTTCCCATGACACAC[A/T]CTGCTGGGCATGTAA	67711
rs32988966	snp	C/G	0.231111	0.249285	synonymous-codon	Nsmce1	Mm_Celera	7:125471230	TGTAGAAGAAGCAAA[C/G]CCAGTTTCTGAGTCA	67711
rs32988971	snp	A/T	0.489796	0.070696	intron-variant	Nsmce1	GRCm38.p3	7:125471392	AGGTGCTAGGTATCC[A/T]ATGTGCACACAGGTT	67711
rs32989005	snp	A/G	0.48	0.0979796	intron-variant	Nsmce1	GRCm38.p3	7:125468638	GATCAAGAGAAGCAT[A/G]TTATAAGCCAGAGAA	67711
rs32989007	snp	G/T	0.231111	0.249285	intron-variant	Nsmce1	Mm_Celera	7:125468707	TATAGAAGATCAGTA[G/T]GGAGCCTGGTTGTCC	67711
rs32989010	snp	C/T	0.497778	0.0332592	intron-variant	Nsmce1	GRCm38.p3	7:125468720	TATGGAGCCTGGTTG[C/T]CCAAGATAATCAAAA	67711
rs32989013	snp	G/T	0.32	0.24	intron-variant	Nsmce1	Mm_Celera	7:125468776	GACTGAGTCGTAGGG[G/T]ACCCTGCAAAGCAGA	67711
rs32989225	snp	C/T	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125475016	AAAGCCTCTCTTAGT[C/T]ACTCCAGATGGCCTG	67711
rs32989228	snp	C/G	0.497778	0.0332592	intron-variant	Nsmce1	GRCm38.p3	7:125475042	GCCTGCACAGCTCTC[C/G]GTGGTGCCCTCTAAT	67711
rs32989231	snp	C/G	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125475270	AAGCTGGCCAGCTCT[C/G]GGGTCTCTCTTGTGC	67711
rs32989335	snp	C/T	0.48	0.0979796	intron-variant	Nsmce1	GRCm38.p3	7:125473843	TCCCAGGTACCAACT[C/T]TGAAAGACTGATACT	67711
rs32989338	snp	C/T	0.48	0.0979796	intron-variant	Nsmce1	GRCm38.p3	7:125473855	ACTTTGAAAGACTGA[C/T]ACTAATTCTGACAAG	67711
rs32989341	snp	A/T	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125473904	GCCACTGTAATAGAA[A/T]CAACATGGCTTCCCA	67711
rs32989506	snp	C/T	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125484843	AAGTTCCTCTTCCAC[C/T]GCTGTTCAGGCAAAG	67711
rs32989508	snp	A/G	0.48	0.0979796	intron-variant	Nsmce1	GRCm38.p3	7:125484989	CGCCAGCAAGCACTG[A/G]CAAGCTTCAGTAGGC	67711
rs32989513	snp	C/T	0.497041	0.0383476	intron-variant	Nsmce1	GRCm38.p3	7:125485050	GCTTCTGCGAATTAG[C/T]TCCCTCCCGGGATGT	67711
rs32989524	snp	C/T	0.21875	0.248039	intron-variant	Nsmce1	Mm_Celera	7:125480476	TTTAAATATTTAAAG[C/T]GTTAAAGTAACCTTA	67711
rs32989526	snp	A/T	0.473373	0.11227	intron-variant	Nsmce1	GRCm38.p3	7:125480480	AATATTTAAAGTGTT[A/T]AAGTAACCTTATATG	67711
rs32989531	snp	C/T	0.260355	0.249785	intron-variant	Nsmce1	GRCm38.p3	7:125481280	CAGTGATGCAGGCCT[C/T]ATAAACTAAGGGCAT	67711
rs32989533	snp	A/G	0.408163	0.193609	intron-variant	Nsmce1	GRCm38.p3	7:125481291	GCCTCATAAACTAAG[A/G]GCATAGGCACTCCCT	67711
rs32989694	snp	C/T	0.497778	0.0332592	intron-variant	Nsmce1	GRCm38.p3	7:125471443	ATTCTCCACACACTG[C/T]AGACAGCCTAGGAGC	67711
rs32989697	snp	A/G	0.497778	0.0332592	intron-variant	Nsmce1	GRCm38.p3	7:125471464	GCCTAGGAGCACCAC[A/G]AAATGGTTAAACTAG	67711
rs32989700	snp	A/G	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125471591	AGAACGTCTTAGCCA[A/G]GTGTGTGGCACATGG	67711
rs32989703	snp	A/G	0.497778	0.0332592	intron-variant	Nsmce1	GRCm38.p3	7:125471603	CCAGGTGTGTGGCAC[A/G]TGGGCTGAGCACACT	67711
rs32989756	snp	C/T	0.391111	0.206368	intron-variant	Nsmce1	GRCm38.p3	7:125468860	GTATCAGCCAGCACC[C/T]AACAGTACCCTGGGA	67711
rs32989758	snp	A/G	0.375	0.216506	intron-variant	Nsmce1	GRCm38.p3	7:125468975	GTATATAGTAACAGT[A/G]GAGGTCCAGTGGGCT	67711
rs32989761	snp	A/G	0.231111	0.249285	intron-variant	Nsmce1	Mm_Celera	7:125469273	TCCCAGCCAACCAAT[A/G]TCAGCAAAGTCCCCT	67711
rs32989974	snp	A/C	0.132653	0.220748	intron-variant	Nsmce1	Mm_Celera	7:125475301	TACCACTCAGCATCA[A/C]GGTCATTGTTCTGCC	67711
rs32989977	snp	C/T	0.459184	0.136902	intron-variant	Nsmce1	GRCm38.p3	7:125475310	GCATCAAGGTCATTG[C/T]TCTGCCTTTATTGCT	67711
rs32989980	snp	C/T	0.375	0.216506	intron-variant	Nsmce1	Mm_Celera	7:125475372	GCAAACCTGCAGAGC[C/T]ACACATGCCCCGAAC	67711
rs32989983	snp	A/G	0.497778	0.0332592	intron-variant	Nsmce1	GRCm38.p3	7:125475433	CAGGCATGAAATCCT[A/G]CTGTGAAAGATTTAA	67711
rs32990014	snp	A/G	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125473907	ACTGTAATAGAAACA[A/G]CATGGCTTCCCAGGG	67711
rs32990017	snp	G/T	0.473373	0.11227	intron-variant	Nsmce1	Mm_Celera	7:125473948	TTACACACTCAGGAA[G/T]GAAGGAGGATGTGTC	67711
rs32990020	snp	A/G	0.473373	0.11227	intron-variant	Nsmce1	Mm_Celera	7:125473959	GGAAGGAAGGAGGAT[A/G]TGTCCGGCGCTGGCT	67711
rs32990023	snp	A/C	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125473996	CAAGGAGGAACTGGC[A/C]CTGAACAGATGAACT	67711
rs32990286	snp	C/G	0.48	0.0979796	intron-variant	Nsmce1	GRCm38.p3	7:125485252	GAACGCTTCCCTCTT[C/G]TCCACTCCTCCAAGT	67711
rs32990289	snp	A/G	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125485336	CATGTTATTGTTCTC[A/G]TTGTTAAAATTAGAA	67711
rs32990292	snp	A/G	0.5	0	intron-variant	Nsmce1	GRCm38.p3	7:125485369	ACAGAAAGGGAAACA[A/G]AACTGCAGAACAAAA	67711
rs32990296	snp	A/G	0.408163	0.193609	intron-variant	Nsmce1	GRCm38.p3	7:125481321	TTCTCATCACAGTTC[A/G]CTCAGTCAGGGCAGA	67711
rs32990299	snp	A/G	0.459184	0.136902	intron-variant	Nsmce1	GRCm38.p3	7:125481402	GACTTTATATAACAC[A/G]ACATCTTGGGACGAG	67711
rs32990301	snp	A/C	0.391111	0.206368	intron-variant	Nsmce1	GRCm38.p3	7:125481477	AATGACAGGCTAAAG[A/C]TAATTTTACGTAACA	67711
rs32990446	snp	C/T	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125471650	AAACCGTCCAGTGAG[C/T]GCCTCATTAAAGTGC	67711
rs32990449	snp	C/G	0.231111	0.249285	intron-variant	Nsmce1	Mm_Celera	7:125471766	TAAGGCCTGTCACTC[C/G]CTGTGAGACCCAGGA	67711
rs32990452	snp	A/G	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125471788	GACCCAGGAAGCTGG[A/G]AAGCATGACAGTGGC	67711
rs32990494	snp	C/T	0.231111	0.249285	intron-variant	Nsmce1	Mm_Celera	7:125469334	GTCAGACAATGGAGG[C/T]GAAGGTCTTCTTACC	67711
rs32990497	snp	C/T	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125469349	CGAAGGTCTTCTTAC[C/T]CTCCAGATCTCAGAA	67711
rs32990499	snp	A/G	0.32	0.24	intron-variant	Nsmce1	Mm_Celera	7:125469408	CCCATCTTCACAGCC[A/G]CCCTACAAGCTAGTC	67711
rs32990502	snp	A/G	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125469436	GTCACAGTTGGTGTC[A/G]TCAGCAAGAGAAGAC	67711
rs32990596	snp	C/G	0.497778	0.0332592	intron-variant	Nsmce1	GRCm38.p3	7:125475696	AGGCTGTGATCATGA[C/G]ACTGTAATTAATGCA	67711
rs32990598	snp	C/T	0.142012	0.225474	intron-variant	Nsmce1	Mm_Celera	7:125475712	ACTGTAATTAATGCA[C/T]CGTGCAGCCTGCTGG	67711
rs32990601	snp	A/G	0.124444	0.216185	intron-variant	Nsmce1	Mm_Celera	7:125476106	ACATTGGCATGCACG[A/G]CATCAGTTCAGTCAT	67711
rs32990686	snp	A/G	0.132653	0.220748	intron-variant	Nsmce1	Mm_Celera	7:125474089	CCAGCCCCAAGTCAT[A/G]CTTAGAACAATTTAT	67711
rs32990689	snp	C/G	0.152778	0.230321	intron-variant	Nsmce1	GRCm38.p3	7:125474106	TTAGAACAATTTATA[C/G]AGAGACAGGTAGAGA	67711
rs32990692	snp	C/T	0.426035	0.177515	intron-variant	Nsmce1	GRCm38.p3	7:125474143	GTCTGTCCTCTTGGG[C/T]AGATGGGAGACTTAC	67711
rs32990984	snp	C/T	0.391111	0.206368	intron-variant	Nsmce1	GRCm38.p3	7:125485386	ACTGCAGAACAAAAG[C/T]GAACACCTGTAGTCA	67711
rs32990986	snp	A/G	0.260355	0.249785	intron-variant	Nsmce1	Mm_Celera	7:125485387	CTGCAGAACAAAAGC[A/G]AACACCTGTAGTCAA	67711

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