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
rs6185108	snp	C/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77357795	ACAGTCTTCCCTTTA[C/G]TTTAATACATAAATA	78514
rs6185186	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77357834	AATGTATTTAATAAA[C/T]AGCTTTCCTTACTGT	78514
rs6185625	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77357856	CCTTACTGTTGCTAC[A/G]TAGTGTATAATGGAA	78514
rs6186131	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77357963	taacagccccacggg[C/T]tcatatatttgaang	78514
rs6186140	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77357977	gntcatatatttgaa[C/T]gtttgggcccccgtg	78514
rs6211445	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77332485	GAGAATGGCTTCCTC[A/G]GAGCTGTATCACCTA	78514
rs6211992	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77332608	TTTGAGACCTTGATA[C/T]GGNGAGCAAGCAGGG	78514
rs6211997	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77332611	GAGACCTTGATANGG[C/T]GAGCAAGCAGGGCAC	78514
rs6212029	snp	G/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77332630	CAAGCAGGGCACCAG[G/T]CTTTACTGGGAAGGC	78514
rs6289772	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77456309	GGACTGGCCTCAAAC[A/G]TTCTTTCAAGTTTTC	78514
rs6289856	snp	A/G	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77456361	AGCACCTTACACTGT[A/G]GCTACAAGTAAGTAA	78514
rs6290853	snp	A/G	0.46875	0.121031	intron-variant	Arhgap10	GRCm38.p3	8:77456508	CGCTAGGAACAGCTC[A/G]TGGGCCAACAGTATC	78514
rs6292365	snp	C/T	0.459184	0.136902	intron-variant	Arhgap10	GRCm38.p3	8:77450194	GAAACCCTTGACGCT[C/T]CATTGCTGAGTTCAC	78514
rs6292366	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77450195	AAACCCTTGACGCTN[C/T]ATTGCTGAGTTCACG	78514
rs6292988	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77450332	CCAGACCTGAGTTCT[A/G]GCCACCCTCACAAGA	78514
rs6293019	snp	C/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77450356	CACAAGACAAGAAAT[C/G]CAGACATAAGGCTCA	78514
rs6293472	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77450386	AAAAAGCATCCTTCC[A/G]CTCTCTCNGTCCTGC	78514
rs6293481	snp	G/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77450394	TCCTTCCNCTCTCTC[G/T]GTCCTGCCTTCAGCT	78514
rs6293540	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77450436	TACATGCAAGTCAAA[A/G]GCTCTTGCTAACACA	78514
rs6293568	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77450455	CTTGCTAACACAAAG[C/T]ACAAGNGCCACCCAG	78514
rs6293579	snp	A/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77450461	AACACAAAGNACAAG[A/T]GCCACCCAGCCTTCG	78514
rs6308440	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77332282	GCTGCTTGCCTAAAA[C/T]GATTCAGATGCTACT	78514
rs6386455	snp	G/T	0.429688	0.173817	intron-variant	Arhgap10	Mm_Celera	8:77420425	ACATAAAGGTCTATC[G/T]CCATGCCTGTAACAG	78514
rs6386905	snp	C/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77420479	GGCGGGGGGGCTGTG[C/G]CCCTCACTGGGGTGA	78514
rs6386974	snp	C/T	0.290657	0.246672	intron-variant	Arhgap10	Mm_Celera	8:77420525	AACAGGGCCTCCCAA[C/T]GGTTTAGATGTTTCT	78514
rs6387986	snp	C/T	0.375	0.216506	synonymous-codon	Arhgap10	Mm_Celera	8:77420694	GAGCTTGCACACATA[C/T]TCAAGCGAGAGCTCG	78514
rs6388493	snp	C/T	0.304688	0.243945	intron-variant	Arhgap10	Mm_Celera	8:77420810	CAAGCTGGAGGTCAA[C/T]GGCCTGGTGCTGGCC	78514
rs6389100	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77420964	AAGAGCTTGATGACC[C/T]NCAAAGACTGAAGAT	78514
rs6389102	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77420965	AGAGCTTGATGACCN[C/T]CAAAGACTGAAGATT	78514
rs6389524	snp	A/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77420992	GATTAAGGAAAACAC[A/T]TCTTCCTGGAACAGT	78514
rs13479846	snp	A/T	0.375	0.216506	synonymous-codon, intron-variant	Arhgap10	Mm_Celera	8:77259128	TCTGGGTGAAGGAGG[A/T]GTTCCAGCTGGGTTG	78514
rs32532686	snp	A/G	0.265928	0.249492	intron-variant	Arhgap10	GRCm38.p3	8:77349009	AGAATGAACTACCTC[A/G]TAAGCTGAAAGGCAA	78514
rs32534714	snp	A/C	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77400736	AACTGTGGCTCCTTC[A/C]GATCCCACGCCTAGG	78514
rs32536777	snp	C/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77286450	AGAAAGCACTTCATT[C/G]GTTAGTTTCAGAGGA	78514
rs32538134	snp	C/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77478400	GTTGTCAGGTGCCTG[C/G]TCTAAAACCAAAGAA	78514
rs32542727	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77280701	AAAAGTCTATGCTGG[A/G]AGGCCAGGAAGCCAG	78514
rs32545086	snp	A/C	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77287407	CACAAACAGCTACCA[A/C]ACCATAGTGGCCTCT	78514
rs32548374	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77278741	AAGCATAAGACAAAT[C/T]GTGGGCCCTGAGTAA	78514
rs32548786	snp	G/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77410798	GCCTAGCATAGGAAG[G/T]AGTCTTCTCTTCTAA	78514
rs32556657	snp	A/T	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77280015	CCAGAAGCCAAGGAT[A/T]CCTAGACTGCCATTC	78514
rs32556769	snp	C/T	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77451819	AGGCTCCGCCATCAG[C/T]GGTCAGGAAACGGAA	78514
rs32565587	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77351112	AGTTCACCAGCTACC[A/G]GCTTCATTTCATTCC	78514
rs32566013	snp	A/C	0.465374	0.126941	intron-variant	Arhgap10	GRCm38.p3	8:77470451	ACTATCTAACTATCG[A/C]CAGCTCTGATTGCTC	78514
rs32566365	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77334311	ATGAGAAGAGAAAGG[A/G]AAGCTACTTAAGGGA	78514
rs32568156	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77342174	GGACCAAGGGATCAT[A/G]GAGAGCCAAGCCACA	78514
rs32572495	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77331357	CCGTGGCTAAGTCAT[A/G]TCCGCTCTCTAAGCC	78514
rs32573254	snp	C/T	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77444705	TCTTCACTCTGAGCA[C/T]CCTCTATACTGAGCC	78514
rs32573795	snp	A/G	0.493827	0.0552116	intron-variant	Arhgap10	GRCm38.p3	8:77482290	TCCTTTAACCATACT[A/G]TACAGACAGCACAAA	78514
rs32575619	snp	G/T	0.33241	0.236027	intron-variant	Arhgap10	Mm_Celera	8:77314962	TTGGTTATTCCTGTA[G/T]ACTTCTGGCAGCTCC	78514
rs32577176	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484696	GGGCATGGTGGTACA[C/T]GCCTTTAATCCCAGC	78514
rs32577381	snp	C/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77321493	ACCAACGACCCCGAG[C/G]CTTACTCAAAGGTGG	78514
rs32578334	snp	C/T	0.33241	0.236027	intron-variant	Arhgap10	GRCm38.p3	8:77490901	ACACATGCTCTTTAT[C/T]CTTAGGTGTGTGGTG	78514
rs32579538	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77349063	CAGGTAGATGCTACC[A/G]GCTTTGCACAAGTGA	78514
rs32582343	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77509841	CTTGACATTGTTATG[A/G]GCTGAGGTGGGGAAA	78514
rs32583244	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77354753	CTCCCAGCCTCCCAC[C/T]GGGCCACCCATCAGA	78514
rs32585101	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77472169	ATATATATATACACA[C/T]ATATACATATACACA	78514
rs32585804	snp	G/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77479883	GTTGTTGTTGTTGTT[G/T]TTTTTAAATATAGCC	78514
rs32587577	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77435705	ATCCACAGTTCTGGG[A/G]TTCTACCTGAGCTCG	78514
rs32587955	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77490409	TCACATGATTTTTAA[C/T]AGACACTTTTAAACT	78514
rs32589562	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77443006	CTTTTGTGTAGTTTT[A/G]TATCAGGTTTTCGGA	78514
rs32591453	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77444558	GCGCTGAGCGCATCC[A/G]CTCAAGAAGACCAAA	78514
rs32593254	snp	A/T	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77465421	CCCCACAGGCCTGAA[A/T]CTACCTTCCCCTACT	78514
rs32595629	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77338503	CTAGCACTCTTCCCA[C/T]TGGCTGACTCCTAGC	78514
rs32596259	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77310485	ACAAGTCTCCCAAAA[A/G]AGAAATTTAAGCTGT	78514
rs32598934	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77357065	TCAAAGACCAGCAAG[C/T]ACAGGAATTATCAAT	78514
rs32603497	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77428181	GCCCTCCCCAGAAGC[A/G]ACTGTGACAGACCTG	78514
rs32603831	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77371455	GCTGGGGAGATGGTT[C/T]AGTAAGCGAACTTAT	78514
rs32604318	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77367815	AGAAACACACAGAGA[C/T]GAAGTTAAGAATGTC	78514
rs32614335	snp	A/G	0.493827	0.0552116	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485355	AACCAGTTACTCCAC[A/G]GACCACGAGAAACAG	78514
rs32615022	snp	A/C	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77328863	GACAGACCACCACAG[A/C]GTAAGGCCTGAACAG	78514
rs32617658	snp	G/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77509515	GAGGAAGAGGAAGAG[G/T]GAAAAGAAAATAGGG	78514
rs32620956	snp	A/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77428851	TCTTACTAAGACTTT[A/T]ACATTTTCATAAAAA	78514
rs32621134	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77357025	CTTGCAGGGGGCAGG[A/G]AGGACTGTATGCCTT	78514
rs32623142	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77410080	AAAATGGAAGCTATC[A/G]CTAAGGAGAACTGCC	78514
rs32623496	snp	A/G	0.46875	0.121031	intron-variant	Arhgap10	GRCm38.p3	8:77508069	TCACATTAATATGTC[A/G]ATGGCATCCCGCTCC	78514
rs32627264	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77304677	CGGTCGTGAGAACGC[A/G]TGTAAGAAGGTAACC	78514
rs32627635	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77321443	TGAGCATACATCACC[C/T]CCCAAAGCAGAGCCT	78514
rs32631717	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77352148	GTGGTCCCCAACCCC[C/T]TTGGGGCTGGATATC	78514
rs32633665	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77336953	AAACATATTTATCAG[C/T]TAAGGAACAGGCTTT	78514
rs32635041	snp	A/T	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77464941	AATAGATCTTTTTTT[A/T]AAAAAAGTGCCTTAC	78514
rs32635049	snp	C/T	0.345679	0.230967	intron-variant	Arhgap10	Mm_Celera	8:77408946	ACTACACACACCAAA[C/T]AGCTTTATCTAAAAT	78514
rs32637461	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77333415	AAAGACAGAGCCAGC[A/G]TTTCTTCATTACCCT	78514
rs32644816	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77262910	TGGAGAATAGGAAAC[A/G]TTGATGAGAGGAGAT	78514
rs32645327	snp	A/C/G	0.625	0.125	intron-variant	Arhgap10	GRCm38.p3	8:77477025	ATGTTGAAGCCCTAC[A/C/G]CCCCTTCTCCCCAGT	78514
rs32646960	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77426068	GGGACTAGAGGTGTG[C/T]GCCACTGTGCCCTGT	78514
rs32650619	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77277508	TCAGAGCTGTTATAG[C/T]GTGGATATTGAATGT	78514
rs32650977	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77442479	TGAGATAGTCAACCC[A/G]GCTGGTTCCAATAAC	78514
rs32651306	snp	G/T	0.401235	0.199068	intron-variant	Arhgap10	GRCm38.p3	8:77358791	GACTGCAGAAAGCCT[G/T]CGGGAAAGACAAAAG	78514
rs32651894	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77344871	GCATTCAATAATCTG[C/T]ATTTTCCTTAACAAT	78514
rs32655111	snp	G/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77484317	TCAATCTCATACTTA[G/T]GCTCCCAATTTTCTA	78514
rs32655825	snp	A/C	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77371697	TCCCAGGTCTGCTCT[A/C]CACCCCTTACGCACA	78514
rs32655921	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77337143	TGAGGGCGCTGGCAG[C/T]GAGGCTGAAGAGATC	78514
rs32659469	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77508147	TTTTTTTTTTTTTTT[C/T]TCTCTTTTGATAGAA	78514
rs32660734	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77443289	TTTATACCATTTATG[A/G]TGTAAATTCACATTC	78514
rs32664122	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77455270	TGCTTTCACATAACG[C/T]AGAAGCACCTGCCAG	78514
rs32667461	snp	C/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77429737	AAAGCTGGATGGGGT[C/G]CATCCCAGATCTCTG	78514
rs32670959	snp	A/G	0.387812	0.208586	intron-variant	Arhgap10	Mm_Celera	8:77329413	TACAGGGCTAGGTTC[A/G]GAGAAAATCAAGATG	78514
rs32689698	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77450237	AAAGCGCCAGGCCCT[C/T]GGAGCACACTGAATG	78514
rs32693085	snp	C/T	0.495868	0.0452663	intron-variant	Arhgap10	GRCm38.p3	8:77510656	GGTGTAGGCCAGGAC[C/T]GCCCACCAGCTCTGG	78514
rs32693201	snp	G/T	0.493827	0.0552116	intron-variant	Arhgap10	Mm_Celera	8:77408798	ACAACTAGTCTTCAG[G/T]GAATTTACTCATGGG	78514

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