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
rs6238463	snp	A/C	0.375	0.216506	intron-variant	Ahctf1	Mm_Celera	1:179775618	AGAAATCACTAAAGT[A/C]AAAATTAGATAAGTG	226747
rs6290121	snp	A/G	0.444444	0.157135	intron-variant	Ahctf1	GRCm38.p3	1:179751558	AATGCTTAGTTCCAG[A/G]TTCACTTTGGCTTCC	226747
rs6290143	snp	A/G	0.429688	0.173817	intron-variant	Ahctf1	GRCm38.p3	1:179751576	CACTTTGGCTTCCAC[A/G]GAGGCTAATGAGCCT	226747
rs6290155	snp	C/T	0.5	0	intron-variant	Ahctf1	Mm_Celera	1:179751585	TTCCACNGAGGCTAA[C/T]GAGCCTGCTCTAACA	226747
rs6290746	snp	C/T	0.5	0	intron-variant	Ahctf1	Mm_Celera	1:179751690	cagagtcttgccaca[C/T]agcccaaggtggcct	226747
rs6354974	snp	A/T	0.444444	0.157135	intron-variant	Ahctf1	GRCm38.p3	1:179760844	CCTGGGCAAGTCTGC[A/T]CTGCATGCAGTTCCG	226747
rs6356510	snp	C/T	0.475309	0.108333	intron-variant	Ahctf1	GRCm38.p3	1:179761139	GCAAAGTCTCAAATG[C/T]CCCAGAATAGTTTTT	226747
rs6357059	snp	A/C	0.5	0	intron-variant	Ahctf1	Mm_Celera	1:179761295	ccacgtaagctacat[A/C]canccccAGTCAGAT	226747
rs6357062	snp	C/T	0.48	0.0979796	intron-variant	Ahctf1	GRCm38.p3	1:179761298	CGTAAGCTACATCCA[C/T]CCCCAGTCAGATGAG	226747
rs13471301	snp	A/T	0.244898	0.249948	missense	Ahctf1	GRCm38.p3	1:179748643	GAATTGGTGTCAGAT[A/T]TATCTTCTCAGTTTG	226747
rs13471302	snp	C/T			synonymous-codon	Ahctf1	Mm_Celera	1:179752519	AAAAGATCCATCAGC[C/T]GCAGTCTCAGACCTG	226747
rs13471303	snp	C/T	0.297521	0.245442	missense	Ahctf1	Mm_Celera	1:179752565	TGACATCTAAGAGGA[C/T]ACCTACAAAGAAGTC	226747
rs30462187	snp	C/T	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179772360	AGAGTGCTCATCTAT[C/T]TAGTATGCACCAGCC	226747
rs30467541	snp	C/T	0.492188	0.0620098	intron-variant	Ahctf1	GRCm38.p3	1:179756222	GGCATTTGTGAATGA[C/T]GCAAAACATGATAAC	226747
rs30552463	snp	C/T	0.359862	0.224567	intron-variant	Ahctf1	GRCm38.p3	1:179767413	TGTTGGAAACAACTA[C/T]AGCTAATGGAAAAGA	226747
rs30566728	snp	A/T	0.46875	0.121031	intron-variant	Ahctf1	GRCm38.p3	1:179756598	GCAGATAGCATTAGC[A/T]CTAGAGTAGCTGCCA	226747
rs30603659	snp	C/T	0.401235	0.199068	intron-variant	Ahctf1	GRCm38.p3	1:179773949	TACAATGGCTATCAA[C/T]CACTACCACCATCTG	226747
rs30651778	snp	A/T	0.387812	0.208586	intron-variant	Ahctf1	GRCm38.p3	1:179790903	CCACTGCTAGTGACA[A/T]CATGGCTCTTATCTT	226747
rs30698227	snp	A/C	0.359862	0.224567	intron-variant	Ahctf1	GRCm38.p3	1:179756573	TGATGATGTCATGAT[A/C]GTTACAATAGCAGAT	226747
rs30752204	snp	C/T	0.487535	0.077957	intron-variant	Ahctf1	GRCm38.p3	1:179785368	TATGTGTGTGGCTGA[C/T]TGCCAACTAAAAGGT	226747
rs30764981	snp	C/T	0.487535	0.077957	intron-variant	Ahctf1	GRCm38.p3	1:179790600	CAGGATAAAATCATA[C/T]CATACTAGCTATCAC	226747
rs30853128	snp	A/G	0.475309	0.108333	intron-variant	Ahctf1	Mm_Celera	1:179759060	AGCAAAAAATATTTG[A/G]CTGAGTTGACAAAGA	226747
rs30904605	snp	C/T	0.48	0.0979796	missense, downstream-variant-500B	Ahctf1	GRCm38.p3	1:179753456	GAAACCATGTCATCA[C/T]TCTGGCTGGTATTTA	226747
rs30935257	snp	A/G	0.484429	0.0868505	intron-variant	Ahctf1	Mm_Celera	1:179755842	ACTCTTACTCTGTAT[A/G]CGTTCAACAATGTGT	226747
rs30948345	snp	A/G	0.48	0.0979796	synonymous-codon, nc-transcript-variant	Ahctf1	GRCm38.p3	1:179753818	AGGTGCTGCAGAGTC[A/G]CTTGCCTCAGCTTCT	226747
rs31028142	snp	A/G	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179771113	TCTGGGCACCCCACC[A/G]CTACCCCCAACCCCA	226747
rs31093006	snp	A/G	0.359862	0.224567	intron-variant	Ahctf1	GRCm38.p3	1:179774880	AATATTCAGTATACA[A/G]CAATAGAGGAAGGCA	226747
rs31109591	snp	C/T	0.444444	0.157135	intron-variant	Ahctf1	GRCm38.p3	1:179757518	TTTGCTCTTTCATGT[C/T]CCAAAAGAAAGTATG	226747
rs31147130	snp	A/G	0.456747	0.140554	intron-variant	Ahctf1	GRCm38.p3	1:179760609	TAGCATTAATTTCAC[A/G]CTTAGCTCAGAAGAA	226747
rs31283404	snp	A/G	0.465374	0.126941	intron-variant	Ahctf1	GRCm38.p3	1:179767711	GTGAGTATGAGTACA[A/G]TTCAGGCACCCAGTG	226747
rs31311753	snp	A/G	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179776923	CTGGCCTGCAAGGCA[A/G]TAGAATCCAGATCTT	226747
rs31347114	snp	C/T	0.487535	0.077957	intron-variant	Ahctf1	GRCm38.p3	1:179770386	TTCTCCGTGACTGAA[C/T]CTATCTGATATAATG	226747
rs31351677	snp	C/G	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179771165	ATAGCTTTTGCTGTT[C/G]TGGAATCCACTCTAG	226747
rs31382745	snp	C/T	0.387812	0.208586	intron-variant	Ahctf1	GRCm38.p3	1:179760785	ATTACTAGCGACTAT[C/T]TAAGTATTTTAGTGG	226747
rs31384542	snp	A/C	0.297521	0.245442	intron-variant	Ahctf1	GRCm38.p3	1:179795975	TTATTACATAAACTA[A/C]TGTAAATCCCTCCTG	226747
rs31418801	snp	A/T	0.444444	0.157135	intron-variant	Ahctf1	GRCm38.p3	1:179771443	ACTTAGCATGAACAG[A/T]ACACTGGACCAAAAT	226747
rs31434005	snp	A/G	0.5	0	intron-variant	Ahctf1	Mm_Celera	1:179762015	ACTTAGACAATCCCC[A/G]TCATTGAAAAATAGC	226747
rs31452862	snp	C/T	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179747822	CCTCCATCCCTATAT[C/T]GACAGAGGCACTTGG	226747
rs31473274	snp	C/T	0.46875	0.121031	intron-variant	Ahctf1	GRCm38.p3	1:179755719	ATTCCAGACAAAAAG[C/T]TAGATTCATATAACT	226747
rs31488960	snp	A/G	0.465374	0.126941	intron-variant	Ahctf1	GRCm38.p3	1:179760528	CTTCTCCCTTTTGGC[A/G]GGTCTAACAGGACTC	226747
rs31518140	snp	C/T	0.415225	0.187619	intron-variant	Ahctf1	GRCm38.p3	1:179761921	AGCAAGTACTCTATC[C/T]GTGCATTACTGCTGA	226747
rs31523974	snp	C/T	0.489796	0.070696	intron-variant	Ahctf1	Mm_Celera	1:179758319	AGTATATAAATTACA[C/T]GTCAGGCATTTTACA	226747
rs31552749	snp	C/T	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179773879	GGGAAAACTACACAT[C/T]TTAGATAAAGAAGGG	226747
rs31564574	snp	C/G	0.455	0.143091	intron-variant	Ahctf1	GRCm38.p3	1:179771691	TGGCAGTTACAGTCT[C/G]TCTGTGTCGATTCGA	226747
rs31612611	snp	G/T	0.475309	0.108333	intron-variant	Ahctf1	GRCm38.p3	1:179762393	AAGAAGGCAAGCCAC[G/T]TTCATAAGCTGACAT	226747
rs31647853	snp	A/C	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179764706	TAATGTGGAAAAAAA[A/C]CAAAAACCAAAACCA	226747
rs31659605	snp	G/T	0.375	0.216506	missense, downstream-variant-500B	Ahctf1	GRCm38.p3	1:179753463	TGTCATCATTCTGGC[G/T]GGTATTTACAGTCTC	226747
rs31722991	snp	A/G	0.492188	0.0620098	intron-variant	Ahctf1	GRCm38.p3	1:179756108	CAATCATCCAAATAG[A/G]TACAGATGTTTTCTC	226747
rs31797886	snp	C/T	0.475309	0.108333	intron-variant	Ahctf1	GRCm38.p3	1:179762350	CATACAAGCTGTCAT[C/T]AAATCTTACCTGCTT	226747
rs31817540	snp	C/T	0.415225	0.187619	intron-variant	Ahctf1	GRCm38.p3	1:179749042	ATCCCATGTGGCCTG[C/T]GAGTCTCCATTTCTA	226747
rs31902175	snp	A/G/T	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179764831	GAAGGTTACAAATTC[A/G/T]AGGCCACTCTGAGCT	226747
rs31902182	snp	A/T	0.487535	0.077957	intron-variant	Ahctf1	GRCm38.p3	1:179760638	AACACAAATCATGTT[A/T]AGAGGTTGAGATTTC	226747
rs31903135	snp	C/T	0.432133	0.171253	missense, nc-transcript-variant	Ahctf1	GRCm38.p3	1:179762572	TCACGGGTGAAGGAG[C/T]ACCTTCTGACTTAAA	226747
rs31928546	snp	C/T	0.387812	0.208586	intron-variant	Ahctf1	GRCm38.p3	1:179775160	CTTGGTGAAAGGCAC[C/T]ATGTATTTGTCTTAT	226747
rs31929290	snp	A/T	0.444444	0.157135	intron-variant	Ahctf1	GRCm38.p3	1:179757624	CTGCTCCGTCCCCTC[A/T]CCCTTCCCCTGCCCT	226747
rs31971334	snp	A/C	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179794892	AATATGCACACACAC[A/C]CCCCAAACAAAATGT	226747
rs32011260	snp	G/T	0.290657	0.246672	intron-variant	Ahctf1	GRCm38.p3	1:179765239	TACCAGTCACTACCA[G/T]TTTGGGTTTGTTTTC	226747
rs32014292	snp	A/C	0.487535	0.077957	intron-variant	Ahctf1	GRCm38.p3	1:179767323	ACCTGAAACCCTTAG[A/C]AGCTGTCTCCAGAGT	226747
rs32020851	snp	A/G	0.487535	0.077957	intron-variant	Ahctf1	GRCm38.p3	1:179785441	TTGTATTATTTCTCA[A/G]AAGAAACAAGAAGAA	226747
rs32034146	snp	C/G	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179760838	AGTAGGCCTGGGCAA[C/G]TCTGCACTGCATGCA	226747
rs32044532	snp	C/T	0.475309	0.108333	intron-variant	Ahctf1	GRCm38.p3	1:179780746	GTGAGGCAATGAAGA[C/T]ACAAAAACTAGAATG	226747
rs32046816	snp	A/C	0.444444	0.157135	intron-variant	Ahctf1	GRCm38.p3	1:179792760	GTCCTCTGACCCTCA[A/C]ATGTACACCATGACA	226747
rs32078279	snp	A/G	0.32	0.24	intron-variant	Ahctf1	GRCm38.p3	1:179802429	TTCTAAAGAATCCAC[A/G]CTCTTTAAAAAATGT	226747
rs32090783	snp	C/T	0.48	0.0979796	downstream-variant-500B, intron-variant	Ahctf1, Gm1305	GRCm38.p3	1:179744594	CACATGTGGCAAGAC[C/T]TACTTTTAAGATAAA	226747
rs32099146	snp	A/C	0.444444	0.157135	intron-variant	Ahctf1	GRCm38.p3	1:179761865	TATCCAGAACAGCTA[A/C]GTGTCTGTCAATACA	226747
rs32123384	snp	C/T	0.391111	0.206368	intron-variant	Ahctf1	GRCm38.p3	1:179756351	GAGATGATTTTCACC[C/T]GTGTTTGCCACCATA	226747
rs32156895	snp	C/T	0.32	0.24	intron-variant	Ahctf1	GRCm38.p3	1:179798693	TGCACCACCACCACC[C/T]GGCCCCTTATGAGTT	226747
rs32173950	snp	C/T	0.475309	0.108333	intron-variant	Ahctf1	GRCm38.p3	1:179797326	TTTTATTCTCAGCTA[C/T]ACAAACTACCTACTT	226747
rs32179725	snp	A/G	0.48	0.0979796	intron-variant	Ahctf1	GRCm38.p3	1:179774323	TTAGGTTCATCAGGC[A/G]TGCACGACAGACACT	226747
rs32208066	snp	C/T	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179771211	CTATGTAGACAAGGC[C/T]GCCCTTGGACTTGAG	226747
rs32223507	snp	A/T	0.444444	0.157135	intron-variant	Ahctf1	GRCm38.p3	1:179764666	AGACGGAACCTCTTC[A/T]CCTCAAACCAATAAA	226747
rs32226370	snp	C/T	0.465374	0.126941	intron-variant	Ahctf1	GRCm38.p3	1:179772236	TTTACTCTTGCTTAA[C/T]TATGAAAACTAAAAT	226747
rs32226935	snp	A/G	0.32	0.24	intron-variant	Ahctf1	GRCm38.p3	1:179762461	TTATTTAGTCTTGAC[A/G]TTTTACTATGGTAGG	226747
rs32230434	snp	C/T	0.444444	0.157135	intron-variant	Ahctf1	GRCm38.p3	1:179757642	CTTCCCCTGCCCTTC[C/T]CCACTCTCTCCAACA	226747
rs32243143	snp	A/G	0.32	0.24	intron-variant	Ahctf1	Mm_Celera	1:179771734	CCCAGAGACTCATGG[A/G]CTAACATGTGCTCAC	226747
rs32262309	snp	C/T	0.465374	0.126941	intron-variant	Ahctf1	GRCm38.p3	1:179770772	GACCCTACATTTCTT[C/T]TGAAGTTCATACTGG	226747
rs32266872	snp	A/C	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179761883	GTCTGTCAATACAGC[A/C]CACCACACTCTATAG	226747
rs32302393	snp	C/T	0.484429	0.0868505	missense, downstream-variant-500B	Ahctf1	GRCm38.p3	1:179753483	TTTACAGTCTCTGCA[C/T]GTGGTTCCTTAACAG	226747
rs32315768	snp	A/G	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179797507	CCAGTCTCAGAAGGC[A/G]AAGACATTCAAATCT	226747
rs32330734	snp	A/C	0.487535	0.077957	intron-variant	Ahctf1	GRCm38.p3	1:179767267	CACAGTTAATAGGAT[A/C]TGTCCTCTGAGTTAA	226747
rs32363444	snp	A/C	0.487535	0.077957	intron-variant	Ahctf1	GRCm38.p3	1:179790506	AAATCTGGGTTAAGG[A/C]GAAACTGTTTTTACA	226747
rs32375796	snp	C/G	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179771148	AGACAGGATCTCATT[C/G]TATAGCTTTTGCTGT	226747
rs32382692	snp	A/T	0.487535	0.077957	intron-variant	Ahctf1	GRCm38.p3	1:179784543	ACACTGAGCTATATA[A/T]TCTCAGTCAGTCCTT	226747
rs32400718	snp	C/T	0.391111	0.206368	intron-variant	Ahctf1	GRCm38.p3	1:179757177	TCTGCAGCTCCTGTG[C/T]ATCAGTCTCAATCTT	226747
rs32402518	snp	A/T	0.493827	0.0552116	intron-variant	Ahctf1	GRCm38.p3	1:179796561	AATTAAAAAAAATTA[A/T]GCATATATCCTAAAC	226747
rs32407184	snp	A/G	0.497778	0.0332592	intron-variant	Ahctf1	GRCm38.p3	1:179748077	CTGGCAAGCACTTTA[A/G]TTTTAAACCTTGACT	226747
rs32422936	snp	A/G	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179770377	CCTTTCATTTTCTCC[A/G]TGACTGAATCTATCT	226747
rs32424340	snp	C/T	0.375	0.216506	synonymous-codon, nc-transcript-variant	Ahctf1	GRCm38.p3	1:179776029	GTCATTATGATCTAG[C/T]AGCCAAAATCCTTGA	226747
rs32425436	snp	C/T	0.46875	0.121031	intron-variant	Ahctf1	GRCm38.p3	1:179759348	TGCTAGTGTATACTT[C/T]AAGGTAACCTTACAC	226747
rs32439477	snp	C/T	0.492188	0.0620098	intron-variant	Ahctf1	Mm_Celera	1:179764588	AAACTATTTTCATAT[C/T]AGCATTTAGTGAAAT	226747
rs32476239	snp	C/T	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179772361	GAGTGCTCATCTATT[C/T]AGTATGCACCAGCCT	226747
rs32482229	snp	G/T	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179756142	TATGTCATAATTTTA[G/T]AGCCCAATTAAAAAG	226747
rs32498434	snp	A/G	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179771219	ACAAGGCCGCCCTTG[A/G]ACTTGAGATCTGTCT	226747
rs32498442	snp	A/G	0.444444	0.157135	intron-variant	Ahctf1	GRCm38.p3	1:179756136	CTCAGATATGTCATA[A/G]TTTTATAGCCCAATT	226747
rs32505334	snp	A/C	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179755748	CTCAAAAAGCAAAGA[A/C]TTACCTAGACTTAAA	226747
rs32545224	snp	C/T	0.32	0.24	intron-variant	Ahctf1	GRCm38.p3	1:179771735	CCAGAGACTCATGGA[C/T]TAACATGTGCTCACC	226747
rs32547688	snp	C/T	0.375	0.216506	intron-variant	Ahctf1	GRCm38.p3	1:179765012	AACCATATGGTGGCT[C/T]ACAACCACCCATAAT	226747
rs32553084	snp	A/G	0.487535	0.077957	intron-variant	Ahctf1	GRCm38.p3	1:179760593	TAGGTGAAAAAACCC[A/G]TAGCATTAATTTCAC	226747
rs32572812	snp	C/T	0.492188	0.0620098	intron-variant	Ahctf1	GRCm38.p3	1:179748988	CACAAAGCTACTGAA[C/T]ATTAGTTTGACCCTC	226747
rs32575544	snp	A/G	0.484429	0.0868505	missense, downstream-variant-500B	Ahctf1	GRCm38.p3	1:179753544	AATGTGCAGCCTTTG[A/G]GACTATCACTGCTCC	226747

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