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
rs6302440	snp	C/T	0.359862	0.224567	intron-variant	Fbxo18	Mm_Celera	2:11752470	AGCGCTTCTCTGCAA[C/T]GACACTCCAACAGCA	50755
rs13469410	snp	C/T	0.32	0.24	synonymous-codon, nc-transcript-variant	Fbxo18	Mm_Celera	2:11767431	TACTAAGAAGACACC[C/T]CGCCATCGTTTGTTC	50755
rs27099229	snp	C/T	0.32	0.24	upstream-variant-2KB, intron-variant	Fbxo18, Ankrd16	Mm_Celera	2:11779441	ACTTAATGAAATGCC[C/T]GCCTTCAAGTTATTT	50755
rs27099230	snp	C/G	0.32	0.24	upstream-variant-2KB, intron-variant	Fbxo18, Ankrd16	Mm_Celera	2:11779401	GTCTAATTCCTAAGA[C/G]CCTGTGAACTTCTTT	50755
rs27099231	snp	A/T	0.391111	0.206368	upstream-variant-2KB, intron-variant	Fbxo18, Ankrd16	Mm_Celera	2:11779174	AGACATCTTGCTAAA[A/T]TTCCTGTTCACGATT	50755
rs27099232	snp	A/C	0.244898	0.249948	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Fbxo18, Ankrd16	Mm_Celera	2:11778541	CAGATCTGCTCTAAG[A/C]CTGAACCTGGGTCTT	50755
rs27099233	snp	C/T	0.124444	0.216185	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Fbxo18, Ankrd16	Mm_Celera	2:11778088	ATTCCCAGAAGCTGT[C/T]CGGTGGAGAGCAGAC	50755
rs27099234	snp	C/T	0.231111	0.249285	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Fbxo18, Ankrd16	Mm_Celera	2:11778060	CAGCTACCACCGGAG[C/T]AGCCCAGCAAACATT	50755
rs27099235	snp	A/G	0.244898	0.249948	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Fbxo18, Ankrd16	Mm_Celera	2:11777762	TTCGCCACCGCGGAG[A/G]AGGCGAAGGAAACTT	50755
rs27099236	snp	A/T	0.124444	0.216185	upstream-variant-2KB	Fbxo18, Ankrd16	Mm_Celera	2:11777739	GAGAGCCACGCCCCG[A/T]CTGTGCTTTCGCCAC	50755
rs27099237	snp	C/G	0.444444	0.157135	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Fbxo18, Ankrd16	Mm_Celera	2:11777541	CCCAGACAGCGAGCA[C/G]AGACGACTGCAGACT	50755
rs27099238	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Fbxo18, Ankrd16	Mm_Celera	2:11776987	CTAGTTCCTCGAAAG[A/G]AAGCCAACAAAGCGG	50755
rs27099239	snp	A/C	0.231111	0.249285	intron-variant, upstream-variant-2KB	Fbxo18, Ankrd16	Mm_Celera	2:11776820	TCCTCGTCTCTAAAA[A/C]CTGAATGCTACCTAT	50755
rs27099240	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB	Fbxo18, Ankrd16	Mm_Celera	2:11776617	GCAAGACCACGTGAA[A/G]TCATTTGTAAGGAAG	50755
rs27099241	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB	Fbxo18, Ankrd16	Mm_Celera	2:11776300	TACAAGGGAATTGAA[A/G]GCCTCCAAAGACCTT	50755
rs27099242	snp	C/T	0.124444	0.216185	intron-variant, upstream-variant-2KB	Fbxo18, Ankrd16	Mm_Celera	2:11776210	CCCTTGATCCCTCAA[C/T]GACATCTAAGTACCA	50755
rs27099243	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB	Fbxo18, Ankrd16	Mm_Celera	2:11775988	GAGCTGGCTTTGGTG[A/G]TAATTTCTACAAGTT	50755
rs27099244	snp	C/T	0.244898	0.249948	intron-variant, upstream-variant-2KB	Fbxo18, Ankrd16	Mm_Celera	2:11775884	GATTATTTTAAGAGG[C/T]TCTGTAGAACACCCA	50755
rs27099245	snp	A/G	0.32	0.24	intron-variant	Fbxo18	Mm_Celera	2:11775699	ATGGCTGCTCTAATA[A/G]TTTTTCATACACTGA	50755
rs27099246	snp	A/G	0.142012	0.225474	intron-variant	Fbxo18	Mm_Celera	2:11775551	GGAGAAGGCCGGAGA[A/G]CAGAAGTTGGGTAGC	50755
rs27099247	snp	A/G	0.231111	0.249285	intron-variant	Fbxo18	Mm_Celera	2:11775542	GCAAGAGTTGGAGAA[A/G]GCCGGAGAACAGAAG	50755
rs27099248	snp	A/G	0.231111	0.249285	intron-variant	Fbxo18	Mm_Celera	2:11775478	GCCAAGGGTAGCTAG[A/G]CATGGAGATTGTCAG	50755
rs27099249	snp	A/C	0.473373	0.11227	intron-variant	Fbxo18	Mm_Celera	2:11775299	AATGTGTGACAGAAA[A/C]GTTTCCTTTCTTCAG	50755
rs27099250	snp	C/T	0.18	0.24	intron-variant	Fbxo18	Mm_Celera	2:11775186	AAATATAATTAGGAC[C/T]GTTACAAGAATCTCC	50755
rs27099251	snp	C/T	0.32	0.24	intron-variant	Fbxo18	Mm_Celera	2:11774827	AGATGGGCTGAACGG[C/T]TCATTCTGTGTTCCT	50755
rs27099252	snp	A/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11774457	TTTGCTACGGGGAGT[A/G]TGATAGGAAAGGATA	50755
rs27099253	snp	C/T	0.32	0.24	intron-variant	Fbxo18	Mm_Celera	2:11773995	GGTGTGTTTTCGACT[C/T]TAGGCCCAGAAAGCT	50755
rs27099254	snp	C/T	0.231111	0.249285	intron-variant	Fbxo18	Mm_Celera	2:11773725	TTAGCTCCTAAGCAA[C/T]AGCACCAGGGGCTGG	50755
rs27099255	snp	A/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11773562	GGCTGTGGTGGCTTC[A/G]ACTATCTCACAGTTC	50755
rs27099256	snp	A/C	0.244898	0.249948	intron-variant	Fbxo18	Mm_Celera	2:11772761	GGTTATTGCAACAAA[A/C]GTTATGCTAATTATT	50755
rs27099257	snp	C/G	0.132653	0.220748	intron-variant	Fbxo18	Mm_Celera	2:11772738	GTCATTCTATGTTTG[C/G]AGCTATTGGTTATTG	50755
rs27099258	snp	A/G	0.197531	0.244432	intron-variant	Fbxo18	Mm_Celera	2:11772601	TGAGTACTTAAGATT[A/G]CTGCTTTAAAAAGAA	50755
rs27099259	snp	C/T	0.21875	0.248039	intron-variant	Fbxo18	Mm_Celera	2:11772081	TCTCATTCACATACT[C/T]AGAATGGAAAATCTA	50755
rs27099260	snp	C/T	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11772049	CTACAAACACTTTTA[C/T]CACAGCAAGCAATAA	50755
rs27099261	snp	A/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11772028	CAATCCTGTGTTCCC[A/G]TGTTCCTACAAACAC	50755
rs27099262	snp	G/T	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11771997	GACAGGAAGTACACA[G/T]CAGGCCAACTGCAGC	50755
rs27099263	snp	A/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11771866	AGCTCTGGGCAGTCA[A/G]TTTGATCTTAGAGCT	50755
rs27099264	snp	A/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11771844	AGGAAGGAAGGAAGC[A/G]CTGGGTAGCTCTGGG	50755
rs27099265	snp	C/T	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11771796	GCAGCACTACCATGT[C/T]AGGCACCACAACAGA	50755
rs27099266	snp	A/C	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11771780	ATCTCATTCAGAAGG[A/C]GCAGCACTACCATGT	50755
rs27099267	snp	C/T	0.124444	0.216185	intron-variant	Fbxo18	GRCm38.p3	2:11771749	TGCCTAAAAGGATAC[C/T]GGAGACCTTATGGCC	50755
rs27099268	snp	A/T	0.132653	0.220748	intron-variant	Fbxo18	Mm_Celera	2:11771730	TTACTTGCATACACA[A/T]TAATGCCTAAAAGGA	50755
rs27099269	snp	G/T	0.408163	0.193609	intron-variant	Fbxo18	Mm_Celera	2:11771364	TGCCTAGCATGCACA[G/T]ACTATAAGGCCCCAG	50755
rs27099270	snp	C/G	0.132653	0.220748	intron-variant	Fbxo18	Mm_Celera	2:11770760	GAAACAGGGAAGAGA[C/G]CATAAGGGGCAAAGG	50755
rs27099271	snp	A/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11770745	AAGGGCCCAAGAGAG[A/G]AAACAGGGAAGAGAC	50755
rs27099272	snp	A/C	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11770656	AGTTGTCCAGCCTAT[A/C]AACACTGCATACTGC	50755
rs27099273	snp	A/C	0.32	0.24	missense, utr-variant-5-prime, nc-transcript-variant	Fbxo18	GRCm38.p3	2:11769888	ACTCCGGGCCAAATG[A/C]TGGCAGTCGACCACT	50755
rs27099274	snp	A/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11769539	TGACTGCAGAACACC[A/G]ACTGACTGTGGGCCA	50755
rs27099275	snp	A/T	0.244898	0.249948	intron-variant	Fbxo18	Mm_Celera	2:11769444	AAAAGAAGCGAGTGC[A/T]CTGTAGGAGGGAACA	50755
rs27099276	snp	A/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11769079	CAGGGAAACACTTTA[A/G]TAGGCTCTGAGAAAT	50755
rs27099277	snp	C/T	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11768529	CATCAACTATAATTG[C/T]TCCACAGCAGTTTAA	50755
rs27099278	snp	C/G	0.152778	0.230321	missense, nc-transcript-variant	Fbxo18	Mm_Celera	2:11767605	CATGTCACCCTCAGC[C/G]TCCTGACAGCTGTCC	50755
rs27099279	snp	G/T	0.32	0.24	synonymous-codon, nc-transcript-variant	Fbxo18	GRCm38.p3	2:11767449	TGTCTTCTTAGTAAC[G/T]CCATCCCACTGGCCG	50755
rs27099280	snp	C/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11766680	GGCATAGAAGAGAAC[C/G]GGTTATTAAGACCAA	50755
rs27099281	snp	C/T	0.231111	0.249285	intron-variant	Fbxo18	Mm_Celera	2:11766567	TCTAGAACGATTAGG[C/T]AAAAAAGGAGAGAAG	50755
rs27099282	snp	A/G	0.152778	0.230321	intron-variant	Fbxo18	Mm_Celera	2:11766285	ATGCTACAAAATAAC[A/G]TACTAATTGTACCAC	50755
rs27099283	snp	A/C	0.244898	0.249948	intron-variant	Fbxo18	Mm_Celera	2:11766237	AGATAGAGATCTAAG[A/C]TAGTGTGAAGACTGT	50755
rs27099284	snp	A/G	0.231111	0.249285	intron-variant	Fbxo18	Mm_Celera	2:11766208	AAGCTCAATGTATGG[A/G]TGCCTGAGATCTAAG	50755
rs27099285	snp	A/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11765524	TAACAATAATTAAAA[A/G]CCCTCGGCTAGATCA	50755
rs27099286	snp	C/T	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11765473	AGCTACTCTGGGATA[C/T]GCAGTGAAACTGCAC	50755
rs27099287	snp	A/C	0.444444	0.157135	intron-variant	Fbxo18	Mm_Celera	2:11765138	ACACAACACAACTTA[A/C]CCGACACCGTGGAAA	50755
rs27099288	snp	C/T	0.244898	0.249948	intron-variant	Fbxo18	Mm_Celera	2:11765126	AGTAAGACGAAGACA[C/T]AACACAACTTAACCG	50755
rs27099289	snp	G/T	0.231111	0.249285	intron-variant	Fbxo18	Mm_Celera	2:11764930	TGAGCTACCCACAAC[G/T]TAAATCAGGCTTTCC	50755
rs27099290	snp	A/T	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Fbxo18	Mm_Celera	2:11764123	GAGGTTCAGCACACA[A/T]AGGTCCGAATCCTTT	50755
rs27099291	snp	A/G	0.32	0.24	intron-variant	Fbxo18	Mm_Celera	2:11763192	AAGAAGAGCCACGTT[A/G]AGGGCTAGAGAGATG	50755
rs27099292	snp	C/T	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11763152	TCAATTTCTCTGCCC[C/T]TTTCAAATTACCCAG	50755
rs27099293	snp	C/G	0.244898	0.249948	missense, nc-transcript-variant	Fbxo18	Mm_Celera	2:11762910	TCTCGGTGACATCTG[C/G]CATGGTCACTGTGGA	50755
rs27099294	snp	A/G	0.197531	0.244432	intron-variant	Fbxo18	Mm_Celera	2:11762824	CTCCCATCCTCCAGG[A/G]TGTTACCTATTGCTG	50755
rs27099295	snp	C/T	0.408163	0.193609	intron-variant	Fbxo18	Mm_Celera	2:11762803	CTTGCCACGCTATCC[C/T]AGCATCTCCCATCCT	50755
rs27099296	snp	A/C	0.142012	0.225474	intron-variant	Fbxo18	Mm_Celera	2:11762679	AAGAACATAGAAACT[A/C]GGTGAAGAAATCTTA	50755
rs27099297	snp	G/T	0.391111	0.206368	intron-variant	Fbxo18	Mm_Celera	2:11762443	TATCCCTCTGAAATC[G/T]GACTTCTGAATATGT	50755
rs27099298	snp	C/T	0.391111	0.206368	intron-variant	Fbxo18	Mm_Celera	2:11761984	CATAACTGCCTACCA[C/T]CCACACTTGGGATTT	50755
rs27099299	snp	A/C	0.32	0.24	intron-variant	Fbxo18	Mm_Celera	2:11761779	GTGGGCTACAACATA[A/C]ACCAGCTGAGAAACT	50755
rs27099300	snp	C/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11761480	CACCAGAACTACCGA[C/G]TGTATAAGAAGAGAC	50755
rs27099301	snp	C/T	0.231111	0.249285	intron-variant	Fbxo18	Mm_Celera	2:11760789	TGCACTGTTGCTATG[C/T]GTAAGGTCACACAAA	50755
rs27099302	snp	A/T	0.391111	0.206368	intron-variant	Fbxo18	Mm_Celera	2:11759519	GGACACTCTAAGATC[A/T]GGGCACAAGTGACTC	50755
rs27099303	snp	C/T	0.132653	0.220748	intron-variant	Fbxo18	Mm_Celera	2:11759450	GCAGCAGGGAGGGAT[C/T]ACAGCTAGAAAATAA	50755
rs27099304	snp	C/G	0.32	0.24	intron-variant	Fbxo18	Mm_Celera	2:11759393	CTGCAGGCCACTGCA[C/G]GTGTTTAATAAATGT	50755
rs27099305	snp	C/T	0.21875	0.248039	intron-variant	Fbxo18	Mm_Celera	2:11759391	CACTGCAGGCCACTG[C/T]AGGTGTTTAATAAAT	50755
rs27099306	snp	A/G	0.231111	0.249285	intron-variant	Fbxo18	Mm_Celera	2:11758602	TTGAAAGAGGTGGGA[A/G]ACCAGAAGCAAGAAC	50755
rs27099307	snp	A/G	0.32	0.24	intron-variant	Fbxo18	Mm_Celera	2:11758249	GAAAACAGTAACCAC[A/G]CGATGTGACAGCAGC	50755
rs27099308	snp	A/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11757708	TATTGAGCTTCACAG[A/G]CATTGTGCTATGGAC	50755
rs27099309	snp	C/T	0.391111	0.206368	intron-variant	Fbxo18	Mm_Celera	2:11757297	TGTGAGTACTCCTCA[C/T]AGAAGCAGATGCCAC	50755
rs27099310	snp	A/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11756865	AGATCTCAAGTGCTC[A/G]GAGGGCGAGAGGCTG	50755
rs27099311	snp	C/T	0.32	0.24	intron-variant	Fbxo18	Mm_Celera	2:11756746	GGAAGAGGCGGGACC[C/T]TGAGACCATACTTCT	50755
rs27099312	snp	C/T	0.391111	0.206368	intron-variant	Fbxo18	Mm_Celera	2:11756580	CAGGACATCTTCTAC[C/T]GGACACAGGAAAGCT	50755
rs27099313	snp	A/C	0.124444	0.216185	missense, nc-transcript-variant	Fbxo18	Mm_Celera	2:11756465	TGGCGTCAAAAGAGG[A/C]AAGCAAAGGTTTGCT	50755
rs27099314	snp	A/G	0.391111	0.206368	intron-variant	Fbxo18	Mm_Celera	2:11756366	CTCTTACATAATCAT[A/G]ACGCTGTCTCTACGG	50755
rs27099315	snp	C/T	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11756031	TAAAAATTTCCATTC[C/T]AATAGCATAACATCT	50755
rs27099316	snp	A/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11755915	TTTTCCACAGGGCAG[A/G]CTTTCTATTTTACCA	50755
rs27099317	snp	A/G	0.391111	0.206368	intron-variant	Fbxo18	Mm_Celera	2:11755490	AAAGCAACATGAATG[A/G]CCTGTGGCTTTATCT	50755
rs27099318	snp	C/T	0.32	0.24	intron-variant	Fbxo18	Mm_Celera	2:11755446	CAAGGTTAAGTCTGA[C/T]AGTATACAATGCTAA	50755
rs27099319	snp	C/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11755330	ACAGATGGCTCTTCC[C/G]TACTTGTCTAATTTG	50755
rs27099320	snp	C/T	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11752274	TTCCCTTTCTTACCA[C/T]TGTCTTCAGCTTCTT	50755
rs27099321	snp	C/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11751861	CTCCTGGGAAAAGGA[C/G]GTGAGACTTCCAAAG	50755
rs27099322	snp	A/G	0.391111	0.206368	intron-variant	Fbxo18	Mm_Celera	2:11751623	TATAGAGCACAAGGA[A/G]CTTTGGTGGGAAATA	50755
rs27099323	snp	C/T	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11751433	GTTTATTTACGTTAT[C/T]CACAAATTTACTCTT	50755
rs27099324	snp	C/G	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11751312	CGCCAGGGGCTCACT[C/G]CACAGGACTGTCTCA	50755
rs27099325	snp	C/T	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11750661	TGAGGGACACAAAGG[C/T]GTGGCAGTGCTTCAT	50755
rs27099326	snp	A/C	0.124444	0.216185	intron-variant	Fbxo18	Mm_Celera	2:11750290	AATCTGAGAGGTGTA[A/C]GTACAACGACCAAAT	50755

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