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
rs31922156	snp	A/G	0.244898	0.249948	utr-variant-3-prime	Trim12a	Mm_Celera	7:104299987	CCTTCTTGCTGAGTG[A/G]AATCTTCCCTTAACA	76681
rs31922158	snp	C/T	0.336735	0.234472	utr-variant-3-prime	Trim12a	Mm_Celera	7:104300124	TGCATTGCCATCTAT[C/T]GGTGGCCTAGAGTTT	76681
rs31922160	snp	G/T	0.444444	0.157135	intron-variant	Trim12a	Mm_Celera	7:104300405	AAGGAGAGACTTCAA[G/T]CAGTGACAGTTAGGA	76681
rs31922163	snp	A/T	0.5	0	intron-variant	Trim12a	GRCm38.p3	7:104300869	CTGTGACCTCTGAAA[A/T]GGGGTAAAAATTTAC	76681
rs31922675	snp	A/C	0.5	0	intron-variant	Trim12a	GRCm38.p3	7:104304591	GAAGCCTGCTTCATC[A/C]TCTTCTTGTATGGGA	76681
rs31922678	snp	C/T	0.444444	0.157135	intron-variant	Trim12a	GRCm38.p3	7:104304595	cctgcttcatcatct[C/T]cttgtatgggaatgg	76681
rs31922680	snp	G/T	0.444444	0.157135	intron-variant	Trim12a	GRCm38.p3	7:104304646	CTCTTAGGGAATCTT[G/T]GATAGCCTTTTAGTG	76681
rs31922683	snp	G/T	0.142012	0.225474	intron-variant	Trim12a	GRCm38.p3	7:104304694	AACACACAGACCTCT[G/T]GTCAGCTTTCCTCAG	76681
rs31923026	snp	C/T	0.48	0.0979796	intron-variant	Trim12a	GRCm38.p3	7:104300991	AACAGTCATTTCCCA[C/T]CTGAGATGGTTATAT	76681
rs31923029	snp	A/T	0.46875	0.121031	intron-variant	Trim12a	GRCm38.p3	7:104301004	CACCTGAGATGGTTA[A/T]ATCACCAGTAGCTGG	76681
rs31923174	snp	C/T	0.32	0.24	upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316846	GAACCACGGTCCTTG[C/T]GGATGCTGGGCTAGT	76681
rs31923176	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316917	TGATGAGGTCATAAG[C/T]CTCACTGTTGTTCTT	76681
rs31923179	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316979	TTGATGTTCCCATTC[C/T]TCTGAAATGTTAATA	76681
rs31923182	snp	A/T	0.444444	0.157135	upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104317081	GGCTAGAAATCACTA[A/T]GTGTTTAGAGTGTTT	76681
rs31923915	snp	C/T	0.244898	0.249948	intron-variant	Trim12a	GRCm38.p3	7:104305650	GCATAAGCCATCATA[C/T]GTGCCATTACATTCT	76681
rs31923918	snp	A/G	0.132653	0.220748	intron-variant	Trim12a	GRCm38.p3	7:104305687	AACTCCCTGGCAGAA[A/G]TTAAACACTGATCAC	76681
rs31923920	snp	C/G	0.165289	0.235211	intron-variant	Trim12a	GRCm38.p3	7:104305745	ATCTTCTTCTGTAGA[C/G]TCAGTTTCAGAAGGC	76681
rs31923923	snp	C/T	0.32	0.24	intron-variant	Trim12a	GRCm38.p3	7:104305796	TCCCTTCTGACCAAG[C/T]ATCCTCTGTGGTGCC	76681
rs31924285	snp	C/T	0.32	0.24	upstream-variant-2KB, nc-transcript-variant	Trim12a, Gm15133	Mm_Celera	7:104317306	GGCAGAATTCCACTC[C/T]CAACTCTGCAAAGAT	76681
rs31924288	snp	C/T	0.444444	0.157135	upstream-variant-2KB, nc-transcript-variant	Trim12a, Gm15133	Mm_Celera	7:104317346	CATTTAGTCTGCCAT[C/T]ACCCTCTGACCTCAG	76681
rs31924291	snp	C/T	0.375	0.216506	upstream-variant-2KB, nc-transcript-variant	Trim12a, Gm15133	Mm_Celera	7:104317349	TTAGTCTGCCATTAC[C/T]CTCTGACCTCAGTGA	76681
rs31924802	snp	C/G	0.124444	0.216185	intron-variant	Trim12a	GRCm38.p3	7:104301577	CTTCAAAATGCTTAG[C/G]CAATATGGAGACTCA	76681
rs31924865	snp	C/T	0.42	0.183303	missense, intron-variant	Trim12a	GRCm38.p3	7:104306049	TCCAGTTTTCAAATT[C/T]TTTCTTATCTGCCAT	76681
rs31924868	snp	A/G	0.142012	0.225474	intron-variant	Trim12a	Mm_Celera	7:104306212	CTACCTTTCTTTTAA[A/G]GGATTGTGATATGAA	76681
rs31924871	snp	C/T	0.152778	0.230321	intron-variant	Trim12a	Mm_Celera	7:104306355	TTGGTCTGGGAAGTT[C/T]ACAGAAACCCAGGAA	76681
rs31925064	snp	G/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Gm15133, Trim12a	Mm_Celera	7:104317502	ATTCCCATGGAACAC[G/T]ATTTGAGAGGAAATA	76681
rs31925069	snp	A/G	0.48	0.0979796	intron-variant, upstream-variant-2KB	Gm15133, Trim12a	Mm_Celera	7:104317619	AACACTTGTGAGTTT[A/G]TACTCCAGGTATTCT	76681
rs31925072	snp	A/G	0.5	0	nc-transcript-variant, upstream-variant-2KB	Gm15133, Trim12a	Mm_Celera	7:104317660	CCAAAGCATGGCCAC[A/G]GTTTTGAATGGGCTG	76681
rs31925665	snp	A/T	0.48	0.0979796	intron-variant	Trim12a	GRCm38.p3	7:104301996	TGCAAGCACACAGGG[A/T]GAATTACAATAGAGT	76681
rs31925668	snp	G/T	0.444444	0.157135	intron-variant	Trim12a	Mm_Celera	7:104302632	ACACAAGGAGCTGAT[G/T]ACTGCAAGGGATAGT	76681
rs31925671	snp	C/T	0.444444	0.157135	intron-variant	Trim12a	Mm_Celera	7:104302637	AGGAGCTGATTACTG[C/T]AAGGGATAGTCTGAA	76681
rs31925754	snp	G/T	0.408163	0.193609	intron-variant	Trim12a	GRCm38.p3	7:104312521	AGATTCAATCAATTA[G/T]GAGACATGATCAAGC	76681
rs31925757	snp	A/T	0.48	0.0979796	intron-variant	Trim12a	GRCm38.p3	7:104312579	CACTTAAAAGAATCA[A/T]ACAAGCTGGCCGGTG	76681
rs31925760	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313087	TGAATACCATCACTC[C/T]TACAGTGTCATGTCA	76681
rs31925763	snp	A/C	0.375	0.216506	intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314086	TTGAGAAAGCAAAAC[A/C]CACAAAATCAACCTT	76681
rs31925915	snp	G/T	0.444444	0.157135	nc-transcript-variant, upstream-variant-2KB	Gm15133, Trim12a	Mm_Celera	7:104317723	TGGATTCTACTTGCT[G/T]CCGTGTAAGTACTCT	76681
rs31926354	snp	A/C	0.142012	0.225474	intron-variant	Trim12a	Mm_Celera	7:104302894	GTCTGTGACTTCTTC[A/C]GTTAGGCTTTGAGAC	76681
rs31926357	snp	C/T	0.124444	0.216185	intron-variant	Trim12a	Mm_Celera	7:104303911	CTGGTGTCATAAATG[C/T]CCATGGATCCAATAG	76681
rs31926360	snp	A/G	0.142012	0.225474	intron-variant	Trim12a	Mm_Celera	7:104303917	TCATAAATGCCCATG[A/G]ATCCAATAGATCTCC	76681
rs31926363	snp	A/G	0.132653	0.220748	intron-variant	Trim12a	Mm_Celera	7:104303972	TCTCTACAAATTCAT[A/G]AAAATAAAATTCCAC	76681
rs31926458	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314253	AGGTAGAAAGAGGCT[A/G]TTGCAGTCATGTGCT	76681
rs31926461	snp	C/T	0.48	0.0979796	intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314368	GAAACCTTACAAAAG[C/T]TGGCACTTTGGGGGA	76681
rs31927056	snp	C/G	0.124444	0.216185	intron-variant	Trim12a	Mm_Celera	7:104303993	AAAATTCCACTCCTT[C/G]TTATTTGTGCATGCA	76681
rs31927059	snp	A/C	0.297521	0.245442	intron-variant	Trim12a	Mm_Celera	7:104304015	GTGCATGCAGTGATC[A/C]TTCCAGCCTCTGAAA	76681
rs31927062	snp	A/G	0.124444	0.216185	intron-variant	Trim12a	Mm_Celera	7:104304057	AAGAGTTCAGGAAGA[A/G]CTCACTGTCATCACC	76681
rs31927239	snp	A/G	0.48	0.0979796	intron-variant, upstream-variant-2KB	Trim12a, Gm15133	Mm_Celera	7:104314702	TGTCAAACAGGGTCG[A/G]TGACTAAATAACAGG	76681
rs31927242	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Trim12a, Gm15133	Mm_Celera	7:104314728	ACAGGCTCTCAGTCT[C/T]TGTTACTAAACTGAG	76681
rs31927835	snp	C/G	0.336735	0.234472	intron-variant	Trim12a	GRCm38.p3	7:104304088	AGGAAGACCACAGCA[C/G]CAGAGAGGAAGGGCA	76681
rs31927838	snp	C/T	0.132653	0.220748	intron-variant	Trim12a	GRCm38.p3	7:104304111	GAAGGGCAATGGCTT[C/T]CATGCCTTCTGACTC	76681
rs31927841	snp	A/G	0.124444	0.216185	synonymous-codon	Trim12a	GRCm38.p3	7:104304204	ATGTTCCACATCTGA[A/G]ATGAAGTCTTCTAGC	76681
rs31928095	snp	A/C	0.444444	0.157135	intron-variant, nc-transcript-variant	Trim12a, Gm15133	Mm_Celera	7:104315087	TGTCATAGACAACAA[A/C]GTTCTGGATCTCGTC	76681
rs31928098	snp	G/T	0.444444	0.157135	intron-variant	Trim12a, Gm15133	Mm_Celera	7:104315113	TCGTCGACAAGGTAC[G/T]ATTCAAAATTACAGA	76681
rs31928101	snp	A/G	0.444444	0.157135	intron-variant	Trim12a, Gm15133	Mm_Celera	7:104315305	GATAAACTCACCCAA[A/G]CAAAAGCAATGTTCT	76681
rs31928744	snp	C/T	0.244898	0.249948	missense	Trim12a	GRCm38.p3	7:104304244	TGCTGAGCATGCTCA[C/T]TTTCAGACTCTGCCA	76681
rs31928747	snp	A/G	0.244898	0.249948	missense	Trim12a	GRCm38.p3	7:104304269	CTGCCAGGTTGTTGA[A/G]AATGTCTTCCTTCTC	76681
rs31928749	snp	C/T	0.375	0.216506	missense	Trim12a	GRCm38.p3	7:104304275	GGTTGTTGAGAATGT[C/T]TTCCTTCTCTTGCCT	76681
rs31928751	snp	C/T	0.5	0	missense	Trim12a	GRCm38.p3	7:104304323	TCTTCTCCTCAGAGT[C/T]CATGATATCCCTCAT	76681
rs31928753	snp	C/T	0.5	0	missense	Trim12a	GRCm38.p3	7:104304355	CGTTTAAACTCTGAC[C/T]GAACATTCTGCACAT	76681
rs31928824	snp	A/G	0.444444	0.157135	intron-variant	Trim12a, Gm15133	Mm_Celera	7:104315340	TCAAAGTCTTCAAAA[A/G]TCTGCCCCCTAAAAT	76681
rs31929522	snp	G/T	0.244898	0.249948	downstream-variant-500B	Trim12a	Mm_Celera	7:104299855	CTAGATAAAAATACC[G/T]CTGCTGTCTGGCCTG	76681
rs31929661	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316771	TCCCTTAGCCTCCCC[A/G]GTGCTGGGATCATGA	76681
rs31929663	snp	G/T	0.444444	0.157135	upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316811	GTTGTTGTTCAGTTT[G/T]GCTTTTGACTTCAGT	76681
rs31929956	snp	A/G	0.152778	0.230321	intron-variant	Trim12a	GRCm38.p3	7:104304410	ATAAGAAAAGGGAGA[A/G]CCATTAAGTTTGTCA	76681
rs31930285	snp	C/G	0.18	0.24	utr-variant-3-prime	Trim12a	Mm_Celera	7:104299924	TTGTTTTATTTTCGG[C/G]TCACACATTAATAAA	76681
rs31930288	snp	A/G	0.46281	0.131194	utr-variant-3-prime	Trim12a	Mm_Celera	7:104299931	ATTTTCGGGTCACAC[A/G]TTAATAAAAGTTTCT	76681
rs31930291	snp	C/G	0.277778	0.248452	utr-variant-3-prime	Trim12a	Mm_Celera	7:104299948	TAATAAAAGTTTCTC[C/G]TGTTTCTTTTGAGTT	76681
rs211712734	snp	C/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316274	TCAAGAATGCCACAC[C/T]CCTAATCTTTCCTGA	76681
rs211751499	snp	G/T			utr-variant-3-prime, missense	Trim12a	Mm_Celera	7:104300305	CCACTTCTGCCTGGA[G/T]GAAAGATCTCCCCTT	76681
rs211992562	in-del	-/TTC			cds-indel	Trim12a	GRCm38.p3	7:104301138	CAGGGGCTCGGAACT[-/TTC]TTCTTTGTTCCCTGG	76681
rs212078216	snp	G/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313473	ACACTCCCAAAGACA[G/T]CGGCATACGCATGGA	76681
rs212312591	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104310306	ATAGCTGGGCCTTGA[C/G]GTAGATCAATTCCCA	76681
rs212678214	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309754	CACTAGGGTCATCCT[C/T]ATAGATTCCAGAAAG	76681
rs212876991	snp	G/T			missense	Trim12a	Mm_Celera	7:104307151	TGCTAAACTGGTAAC[G/T]AATTCGGCACACAGG	76681
rs213052059	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104308119	CCTGCCTCTGCCTCC[C/G]AAGTGCTGGGTTTAA	76681
rs213196247	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309974	acctttctgggtctc[C/T]ggattatagttcaat	76681
rs213360521	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104308765	AACCCAGTAGCTGAC[C/T]CAGATAGGTACAGAC	76681
rs213469132	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104311440	TTGAATCTGTAGATT[C/G]CTTTTGCTAGGATGA	76681
rs213940468	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104310334	CCAGTTTTGTGAGGA[A/G]CAGACATATTGATTT	76681
rs214022401	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104309049	AAGCTGTTGTTCTAT[G/T]TGCTGGGCTGCCTTG	76681
rs214046500	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104307474	cacctccatgagatt[A/C]ccgaaccatacaggt	76681
rs214250301	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301971	TGTTAAATCCAGATC[C/T]ACAGCCACATGCAAG	76681
rs214600454	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104301676	AACTAAGACTAATAT[A/C]TTCCCAGTGTCTCAG	76681
rs214771022	snp	C/G			intron-variant	Trim12a	Mm_Celera	7:104303307	gaatttataagccag[C/G]cgcaattaaatgtcc	76681
rs215340827	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104302023	GAGTTAAGAGTACCC[C/T]AATTTTTTAATCCCT	76681
rs215928680	snp	C/G			intron-variant	Trim12a	Mm_Celera	7:104300690	TACAGGCACTGGAGA[C/G]AACTTTGTGCAGAAG	76681
rs216208660	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104307944	aaagaggaaatggat[A/C]aattccttaaagaaa	76681
rs216404109	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301521	AAAAGTGTGTGGAAA[A/G]TATTCACATGAATGT	76681
rs216416382	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104305957	TTGCCAAGGTCCCTC[C/T]TGGGCATCAGGTTGA	76681
rs216472497	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104305530	gtacctacctagacc[A/C]ggttttaccttgtag	76681
rs217171792	snp	A/G			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104317178	AGCTACCATGTCTCT[A/G]TCTTTTCTACATTTT	76681
rs217656564	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301723	AGCTTGGTGTGCCCT[A/G]TGGACACAAGGATAC	76681
rs217721583	snp	C/T			intron-variant	Trim12a	Mm_Celera	7:104303127	ggccttgtaggtctg[C/T]cactgcgggcatggg	76681
rs217821303	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104310430	CTTCACCAACATTAG[A/C]TGTCACTTTTGTTAT	76681
rs217944221	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104312758	AACCAAACAAACAAA[A/C]AAAAAAGAATCATAC	76681
rs217963401	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301592	CCAATATGGAGACTC[A/G]CAAATAACATCTGAT	76681
rs218112553	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301885	CAATGTCTTCTAGCC[C/T]CAGAAGAAAATAGTG	76681
rs218365640	snp	A/G			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316956	CACAATTGCTTACAA[A/G]TAATGCTTTGATGTT	76681
rs218575388	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104312133	agaatcagagccatc[A/G]tacctaattaagtgc	76681
rs218908406	snp	A/G			intron-variant	Trim12a	Mm_Celera	7:104302494	aataaaaaaagaaaa[A/G]aaaagaaaagaaaaa	76681
rs219057059	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104305898	GGAGTATCAAGGTTT[A/C]TTGGCCTCATAAACT	76681

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