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
rs4223811	snp	C/T	0.165289	0.235211	utr-variant-3-prime	Mynn	GRCm38.p3	3:30618441	TAACCAGAAAAAGAT[C/T]AGCTGAACATTTTAT	80732
rs4223812	snp	A/G	0.165289	0.235211	utr-variant-3-prime	Mynn	GRCm38.p3	3:30618282	TGGTCATAATTTACC[A/G]TGAAAATGCTATAGC	80732
rs4223813	snp	A/C	0.165289	0.235211	utr-variant-3-prime	Mynn	GRCm38.p3	3:30618190	GTTCTGTGACTTGGA[A/C]CCAAAGAGGGAGGAT	80732
rs4223814	snp	A/T	0.244898	0.249948	utr-variant-3-prime	Mynn	Mm_Celera	3:30619539	TTCAGATTGGAT[A/T]	80732
rs4223815	snp	C/T	0.244898	0.249948	utr-variant-3-prime	Mynn	Mm_Celera	3:30619551	ATTAACTCTCTACAC[C/T]AATTTTAAAAATATC	80732
rs4223816	snp	A/T	0.35124	0.228584	utr-variant-3-prime	Mynn	Mm_Celera	3:30619577	ATATCCTAGGCTAAT[A/T]GTTGTACTGTCTTTA	80732
rs4223817	snp	A/G	0.244898	0.249948	utr-variant-3-prime	Mynn	Mm_Celera	3:30619618	ATTGGAGTTTAATAA[A/G]AGTACCCATGCCCAC	80732
rs4223818	snp	C/T	0.244898	0.249948	utr-variant-3-prime	Mynn	Mm_Celera	3:30619627	TAATAAGAGTACCCA[C/T]GCCCACTCCAGTTTG	80732
rs4223819	snp	A/C	0.244898	0.249948	utr-variant-3-prime	Mynn	Mm_Celera	3:30619637	ACCCATGCCCACTCC[A/C]GTTTGCTGTGCTGAA	80732
rs4223820	snp	A/C	0.244898	0.249948	utr-variant-3-prime	Mynn	Mm_Celera	3:30619657	GCTGTGCTGAATCAG[A/C]TGTGCTGGGGCAGAT	80732
rs4223821	snp	G/T	0.244898	0.249948	utr-variant-3-prime	Mynn	Mm_Celera	3:30619674	GTGCTGGGGCAGATA[G/T]TTGATAGAGAAGCCT	80732
rs4223822	snp	A/G	0.244898	0.249948	utr-variant-3-prime	Mynn	Mm_Celera	3:30619722	TGGACCAAACACTGA[A/G]AGCTGCCTCCCAAGC	80732
rs4223823	snp	A/T	0.244898	0.249948	utr-variant-3-prime	Mynn	Mm_Celera	3:30619758	TTGGTGCTCTGTCTT[A/T]GAGAAGCACTTGAAA	80732
rs4223824	snp	A/G	0.35124	0.228584	utr-variant-3-prime	Mynn	Mm_Celera	3:30619770	CTTTGAGAAGCACTT[A/G]AAATGACGTTCTGGA	80732
rs4223825	snp	C/T	0.408163	0.193609	utr-variant-3-prime	Mynn	Mm_Celera	3:30619833	ATTTTTAATCTGTTA[C/T]TGAATTAAAAATACC	80732
rs4223826	snp	A/G	0.408163	0.193609	utr-variant-3-prime	Mynn	Mm_Celera	3:30619836	TTTAATCTGTTATTG[A/G]ATTAAAAATACCACC	80732
rs4223827	snp	G/T	0.35124	0.228584	utr-variant-3-prime	Mynn	Mm_Celera	3:30619864	ACCAAATAAAAAGAT[G/T]AATTCTGCATTTTCA	80732
rs4223828	snp	A/C	0.30839	0.243086	downstream-variant-500B	Mynn	Mm_Celera	3:30619893	CACTCACTATTTTGA[A/C]TAACAATGAGATGGA	80732
rs4223829	snp	G/T	0.35124	0.228584	downstream-variant-500B	Mynn	Mm_Celera	3:30619906	GACTAACAATGAGAT[G/T]GAGATATTAGGACAT	80732
rs4223830	snp	C/T	0.44898	0.258145	downstream-variant-500B	Mynn	Mm_Celera	3:30619941	TTCTTTGTTTCTTTT[C/T]TACTTGAGGCAGGTT	80732
rs4223831	snp	C/G	0.277778	0.248452	downstream-variant-500B	Mynn	Mm_Celera	3:30619977	ATGTATCACTCTGTT[C/G]AGATTGGAT	80732
rs6299406	snp	C/G	0.5	0	upstream-variant-2KB	Mynn, Actrt3	GRCm38.p3	3:30600458	agttctgggatGCTC[C/G]GCTCCCCTCCTTCCC	80732
rs6299422	snp	G/T	0.5	0	upstream-variant-2KB	Mynn, Actrt3	GRCm38.p3	3:30600477	CCCCTCCTTCCCCTT[G/T]TCTTTTCTCCGTTCA	80732
rs13469476	snp	A/G			utr-variant-3-prime	Mynn	Mm_Celera	3:30617436	ATTCTGGAGAAAACC[A/G]GTGCTCAGATCCATT	80732
rs13469477	snp	C/T	0.231111	0.249285	missense	Mynn	Mm_Celera	3:30616578	ATCCAGATTGCAGTG[C/T]AGATGACCATGCTGT	80732
rs13477040	snp	C/T	0.448558	0.151903	upstream-variant-2KB	Mynn	GRCm38.p3	3:30602043	GTAGAAAGCCCACCT[C/T]CCTCCCACGTTGCGC	80732
rs30653329	snp	A/G	0.188366	0.242283	utr-variant-3-prime	Mynn	Mm_Celera	3:30618674	CAAGAAGATTAAACA[A/G]GATTCCAAAAGCTGC	80732
rs30858880	snp	C/T	0.5	0	intron-variant	Mynn	GRCm38.p3	3:30610196	ATCTTGCTGTATAGC[C/T]CAGGCTGGTTGCAGA	80732
rs30949246	snp	A/G	0.432133	0.171253	intron-variant	Mynn	GRCm38.p3	3:30609241	GAGAGAGCACGCAGG[A/G]TAAGCCTCACAGGAC	80732
rs30955726	snp	A/G	0.277778	0.248452	intron-variant	Mynn	GRCm38.p3	3:30604753	CAGAGGAAGACACGC[A/G]GAATCGTCTGCGGCT	80732
rs31557465	snp	C/T	0.197531	0.244432	intron-variant	Mynn	Mm_Celera	3:30608931	ATTTTTTTTTCCTAA[C/T]ATGATATCATTGCTC	80732
rs36241083	snp	C/T	0.124444	0.216185	utr-variant-3-prime	Mynn	Mm_Celera	3:30617189	AAACAAAATCTACAG[C/T]AATATCAACTTCGAA	80732
rs36276030	snp	A/G	0.152778	0.230321	intron-variant	Mynn	Mm_Celera	3:30604458	ACCTATCCAAAGCTT[A/G]AATCAAGCCAGAGGC	80732
rs36303765	snp	C/T	0.231111	0.249285	utr-variant-5-prime	Mynn	Mm_Celera	3:30602546	GGCCCTAGTAGACTT[C/T]TAGCGTCCTATCTCC	80732
rs36336408	snp	A/G	0.231111	0.249285	synonymous-codon	Mynn	Mm_Celera	3:30607784	CTTGTGTGGAAAGGC[A/G]TTTACCCAGTGCAAC	80732
rs36358755	snp	G/T	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30606625	GGGATGATGGGACAT[G/T]TGCACGGTCACAGTG	80732
rs36388272	snp	A/T	0.124444	0.216185	intron-variant	Mynn	Mm_Celera	3:30616159	GATTGATTTACTTTG[A/T]TGCCCTTCTGCACTT	80732
rs36399924	snp	C/T	0.244898	0.249948	intron-variant	Mynn	Mm_Celera	3:30608660	TTGGTTTTTGAAGAT[C/T]CTTCTTTCTCAGCTT	80732
rs36401062	snp	A/C	0.124444	0.216185	utr-variant-3-prime	Mynn	Mm_Celera	3:30617953	TGGGTGTAGCGAGTT[A/C]AGCATCGCCCGTCCT	80732
rs36410763	snp	A/G	0.124444	0.216185	synonymous-codon	Mynn	Mm_Celera	3:30616783	TGGGTACTCGGAACC[A/G]CAGTTGATTTTTTTA	80732
rs36454669	snp	C/T	0.124444	0.216185	utr-variant-3-prime	Mynn	Mm_Celera	3:30619509	ATCTTACAGAAATGG[C/T]ACATGTCAAAGCAGT	80732
rs36457490	snp	A/T	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30604580	GGTCCTTAGCCACCA[A/T]ATAAAAGCAGTTTTG	80732
rs36459536	snp	C/G	0.124444	0.216185	missense	Mynn	Mm_Celera	3:30607126	AGATGGAGGATTTCG[C/G]TTTCATTGCTAGTCC	80732
rs36466816	snp	A/T	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30612186	ATAGCAAGATTTGAA[A/T]TGTCACTTGAATTTG	80732
rs36580575	snp	C/G	0.124444	0.216185	utr-variant-3-prime	Mynn	Mm_Celera	3:30617287	GTCTATGAAAATTTA[C/G]ATACTGAGGAAGAAT	80732
rs36583226	snp	C/T	0.124444	0.216185	intron-variant	Mynn	Mm_Celera	3:30615418	ACTGCAGTGAGTCTC[C/T]TCATAGTCCATTTAA	80732
rs36679406	snp	A/G	0.32	0.24	intron-variant	Mynn	GRCm38.p3	3:30616413	TACGTGCTGTGTAGT[A/G]TCAGTGCAAACTTCA	80732
rs36722814	snp	C/T	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30608896	CTTCAAACTTTATGA[C/T]TTTAGCAAGTAAAAC	80732
rs36729783	snp	A/G	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30608638	CGTTACATGCTCCTA[A/G]ATTTCATTGGTTTTT	80732
rs36737794	snp	A/T	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30615444	TTTAATACCTATGGG[A/T]TACACATAGCTGCAG	80732
rs36772969	snp	A/G	0.124444	0.216185	utr-variant-3-prime	Mynn	Mm_Celera	3:30619510	TCTTACAGAAATGGC[A/G]CATGTCAAAGCAGTT	80732
rs36775575	snp	A/G	0.244898	0.249948	intron-variant	Mynn	Mm_Celera	3:30612094	CAAAGTGTACTGGTC[A/G]GAGTCTTTTTTGGAA	80732
rs36852208	snp	A/G	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30615819	TTGCAAACAGAGGGC[A/G]TTTTGATGAGTCACA	80732
rs36860953	snp	A/C	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30606063	AGATGGCTAAATGTC[A/C]ATTTTTATTAACAAG	80732
rs36862600	snp	C/T	0.132653	0.220748	intron-variant	Mynn	Mm_Celera	3:30611398	TGTATACGTGACCTC[C/T]GGATTGCTTTACTTA	80732
rs36870511	snp	C/T	0.124444	0.216185	utr-variant-3-prime	Mynn	Mm_Celera	3:30617422	AGAGTGAATTCAGTA[C/T]TCTGGAGAAAACCAG	80732
rs37003041	snp	A/G	0.132653	0.220748	intron-variant	Mynn	Mm_Celera	3:30602974	GTGTGTCCTCCTCCG[A/G]AGAGTGATGGAACCT	80732
rs37030180	snp	G/T	0.32	0.24	intron-variant	Mynn	Mm_Celera	3:30615117	TCAACATCCTGGCAG[G/T]ATAGGAAGCCAGACT	80732
rs37052890	snp	A/G	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30611946	CTCTGGTGAGTAAGA[A/G]TGTGGATGGGGAGTT	80732
rs37070162	snp	A/G	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30615924	AAGCATGCACTGTTG[A/G]CTATCTAACGAGGCT	80732
rs37075439	snp	A/G	0.231111	0.249285	utr-variant-3-prime	Mynn	Mm_Celera	3:30618132	GTTCAGGACTGCACC[A/G]GAACAGGCTCGCAGT	80732
rs37084778	snp	A/G	0.244898	0.249948	intron-variant	Mynn	Mm_Celera	3:30604233	TTTCCTTTGGTCTTC[A/G]TGTCCCTCAGGCCCT	80732
rs37107474	snp	C/T	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30612560	CCATACAGGTCTGTG[C/T]TGAGGGAGAACGCAT	80732
rs37122592	snp	A/T	0.32	0.24	intron-variant	Mynn	Mm_Celera	3:30613717	CGTTTCAACACTGGA[A/T]ACTAGATCTGTGTTT	80732
rs37150376	snp	A/G	0.32	0.24	utr-variant-3-prime	Mynn	Mm_Celera	3:30618025	TTGATTTCACTTTGC[A/G]TTTTAAGTTCAGTTT	80732
rs37158048	snp	A/C/G	0.231111	0.249285	synonymous-codon	Mynn	GRCm38.p3	3:30607151	TAGTCCCTCTTCTAC[A/C/G]GAAATATCTAGTATT	80732
rs37171711	snp	A/G	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30607987	TCTTCAGCCCATACA[A/G]ATGACATTAGCATAC	80732
rs37204018	snp	C/T	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30613505	TTGTGTGTCAGCTAG[C/T]AATTTTTTAAATACT	80732
rs37226476	snp	C/T	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30613422	CTAAGTGTGTAGGGT[C/T]TCTCATCTCACAGTC	80732
rs37232270	snp	A/G	0.32	0.24	downstream-variant-500B	Mynn	Mm_Celera	3:30620274	TAAGCAGAAATGCTG[A/G]GTGGTGGCTCACAGG	80732
rs37243319	snp	C/T	0.124444	0.216185	intron-variant	Mynn	Mm_Celera	3:30613406	TTAAGTAAAAGTGTA[C/T]CTAAGTGTGTAGGGT	80732
rs37244870	snp	A/G	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30616401	CCCTGTTCTTGATAC[A/G]TGCTGTGTAGTATCA	80732
rs37274346	snp	A/T	0.32	0.24	intron-variant	Mynn	Mm_Celera	3:30613681	TCTCTATTGTGCTGG[A/T]CCTTAGCATGATGAG	80732
rs37361619	snp	C/T	0.231111	0.249285	utr-variant-3-prime	Mynn	Mm_Celera	3:30617152	TGACCTGGGGTTTTT[C/T]GTTGTTCTCTCCTTG	80732
rs37374697	snp	C/T	0.231111	0.249285	synonymous-codon	Mynn	Mm_Celera	3:30607334	GAAGGCCTTCAGTTC[C/T]CAGAAACCAGGGCAG	80732
rs37422288	snp	A/T	0.244898	0.249948	intron-variant	Mynn	Mm_Celera	3:30612833	ACATTTGCATTAAAT[A/T]GAGTAGATATATCAA	80732
rs37466730	snp	A/G	0.32	0.24	utr-variant-3-prime	Mynn	Mm_Celera	3:30617833	ATCAGTTTGTTTACC[A/G]TTTTATATTTGAGTT	80732
rs37470403	snp	A/C	0.132653	0.220748	intron-variant	Mynn	Mm_Celera	3:30610770	CGCATTGGCGCCATG[A/C]ATGTTGGAGTCATTG	80732
rs37491282	snp	A/T	0.244898	0.249948	intron-variant	Mynn	Mm_Celera	3:30612642	CATTGTGGAGTATCT[A/T]GTATCTAGTATAACT	80732
rs37498522	snp	C/T	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30616352	CTGGGCTTGGAATGT[C/T]TACACTCATGTGTGT	80732
rs37513107	snp	A/G	0.32	0.24	downstream-variant-500B	Mynn	Mm_Celera	3:30620204	CAGGAAATGTACAAA[A/G]ATAATTCTGTCCACT	80732
rs37542174	snp	A/C	0.231111	0.249285	missense	Mynn	Mm_Celera	3:30607240	ATCGGGAGAAATCAG[A/C]AGTCTCCACGGACTC	80732
rs37545302	snp	A/G	0.260355	0.249785	intron-variant	Mynn	Mm_Celera	3:30615530	CCTGGATGTAATGTC[A/G]GAGATCTGACTATAT	80732
rs37559115	snp	A/G	0.32	0.24	downstream-variant-500B	Mynn	Mm_Celera	3:30620240	AAAGGCGAGAAAGCC[A/G]AGATCAGTAGCTGTA	80732
rs37591023	snp	C/T	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30604505	TAAGGGTCTTAACCG[C/T]TGGGCTCCAGAGGTG	80732
rs37710630	snp	C/T	0.124444	0.216185	downstream-variant-500B	Mynn	Mm_Celera	3:30620342	GAGAGAAAGGGCCAT[C/T]CATCGTTCACCTGGG	80732
rs38008975	snp	A/T	0.297521	0.245442	intron-variant	Mynn	Mm_Celera	3:30606887	TACATTCTATAAATT[A/T]GTTACTTAGTTTAAA	80732
rs38054137	snp	C/T	0.124444	0.216185	utr-variant-3-prime	Mynn	Mm_Celera	3:30616882	GGTAAGGTGCAGAGT[C/T]GTGTTAACTAACCCC	80732
rs38142517	snp	A/G/T	0.231111	0.249285	synonymous-codon	Mynn	GRCm38.p3	3:30607127	GATGGAGGATTTCGC[A/G/T]TTCATTGCTAGTCCC	80732
rs38209895	snp	A/G	0.244898	0.249948	intron-variant	Mynn	Mm_Celera	3:30615023	TCATTATTGTCCATA[A/G]TGCATTGAGGATGAC	80732
rs38243510	snp	C/T	0.132653	0.220748	utr-variant-3-prime	Mynn	Mm_Celera	3:30618641	TACCTATAATCACAG[C/T]ATTCTGGGAAGTTAA	80732
rs38345253	snp	C/T	0.244898	0.249948	intron-variant	Mynn	Mm_Celera	3:30608603	ACTCAGGCCAATTTT[C/T]ACATATTACCACCAC	80732
rs38364597	snp	A/G	0.142012	0.225474	intron-variant	Mynn	Mm_Celera	3:30616259	TGACTGCGTAGTCAA[A/G]CAAGCCTGAGAAGAG	80732
rs38367535	snp	G/T	0.244898	0.249948	utr-variant-5-prime	Mynn	Mm_Celera	3:30602559	TTTTAGCGTCCTATC[G/T]CCGGTGTCCCCAATG	80732
rs38484787	snp	A/G	0.231111	0.249285	intron-variant	Mynn	Mm_Celera	3:30615165	TTGCTGACATTAGAT[A/G]CTTGGTTTACTGTAC	80732
rs38515421	snp	A/G	0.32	0.24	utr-variant-3-prime	Mynn	Mm_Celera	3:30619137	ACGTGCGTGCACTTT[A/G]TGAGAATCTGGGAGT	80732
rs38699250	snp	G/T	0.231111	0.249285	downstream-variant-500B	Mynn	Mm_Celera	3:30620076	GTACCACTCTCTACA[G/T]TAATCCCTCGAGACA	80732
rs39268738	snp	C/T	0.231111	0.249285	utr-variant-3-prime	Mynn	GRCm38.p3	3:30617384	TTAAAACCCAGAAAA[C/T]GTGTGTAAATTTGTG	80732
rs39307382	snp	C/T	0.124444	0.216185	utr-variant-3-prime	Mynn	Mm_Celera	3:30618256	CTGCAGGTGTCTTCC[C/T]ATTTCTTAAAGCTAT	80732
rs39483723	snp	C/T	0.231111	0.249285	utr-variant-3-prime	Mynn	Mm_Celera	3:30617947	TTCCCCTGGGTGTAG[C/T]GAGTTCAGCATCGCC	80732

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