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
rs6154888	snp	A/G	0.5	0	intron-variant	Arhgef37	Mm_Celera	18:61507381	AAAGTAGATCCAGAA[A/G]GCATACAGCCCCATT	328967
rs6154937	snp	C/G	0.5	0	intron-variant	Arhgef37	Mm_Celera	18:61507404	GCCCCATTTCCTCCT[C/G]ACTTGGCACTCTGCT	328967
rs29538984	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Arhgef37	Mm_Celera	18:61513362	ACTTGATCTTTGACA[A/G]AGACGCCAAAAATAT	328967
rs29551807	snp	C/T	0.304688	0.243945	utr-variant-3-prime	Arhgef37	GRCm38.p3	18:61494089	TTCTTCTACCCAGAA[C/T]CAGGAAATCACACCA	328967
rs29555751	snp	A/G	0.345679	0.230967	intron-variant	Arhgef37	GRCm38.p3	18:61508125	AAAATAAAAGCAAAT[A/G]CATTCAGCCAGGGGG	328967
rs29558132	snp	A/G	0.444444	0.157135	intron-variant	Arhgef37	Mm_Celera	18:61502066	AAACATCTCTCCATA[A/G]GGGAAGGAAGAGAAC	328967
rs29564966	snp	C/T	0.408163	0.193609	intron-variant	Arhgef37	Mm_Celera	18:61521889	GAATCCGGTTACTTA[C/T]AGGGAGAAGGTGGGA	328967
rs29567133	snp	C/T	0.375	0.216506	intron-variant, missense	Arhgef37	GRCm38.p3	18:61505650	TGCCTATCAGGGGAA[C/T]GGGAGGAGATACTGC	328967
rs29567842	snp	C/G	0.492188	0.0620098	intron-variant	Arhgef37	Mm_Celera	18:61502361	ACTGGGAGAGAGTCA[C/G]GACACTACATGTCTA	328967
rs29571872	snp	C/T	0.444444	0.157135	intron-variant	Arhgef37	Mm_Celera	18:61515580	CTGGAACTCACACTG[C/T]AGACCAGGCTGGCCT	328967
rs29572508	snp	C/T	0.375	0.216506	intron-variant	Arhgef37	Mm_Celera	18:61515473	CAGGTTAGCCTTGAA[C/T]TCATAGCAATTCCCC	328967
rs29574262	snp	A/G	0.444444	0.157135	intron-variant	Arhgef37	GRCm38.p3	18:61518819	GATATGAAAGGAGTC[A/G]CAGCATCTTCTCCGT	328967
rs29575194	snp	G/T	0.444444	0.157135	intron-variant	Arhgef37	GRCm38.p3	18:61506163	TAACTGTTCTTGCAG[G/T]GAACCTGGGTTTGGT	328967
rs29582459	snp	A/G	0.375	0.216506	intron-variant, utr-variant-5-prime	Arhgef37	GRCm38.p3	18:61511934	GGAACAGAGGCATGG[A/G]AGCAGGAATACCTGA	328967
rs29588358	snp	A/G	0.375	0.216506	intron-variant	Arhgef37	Mm_Celera	18:61520794	AAACAAAACAAAAAA[A/G]CAACAACAAAAAACA	328967
rs29623808	snp	A/G	0.444444	0.157135	intron-variant	Arhgef37	Mm_Celera	18:61508430	CAACCTGAGAGGTGG[A/G]TGCATCCAGCCACTC	328967
rs29666140	snp	C/T	0.375	0.216506	upstream-variant-2KB, utr-variant-5-prime, intron-variant	Arhgef37	GRCm38.p3	18:61536539	TCTGGGAAGCTCCAC[C/T]GTCTGCTGTGCACGC	328967
rs29670090	snp	A/G	0.5	0	utr-variant-3-prime	Arhgef37	GRCm38.p3	18:61493994	TGTGTCCTACGTCTT[A/G]GGCCTCACATCTACC	328967
rs29676133	snp	C/T	0.444444	0.157135	intron-variant	Arhgef37	GRCm38.p3	18:61511653	CCAGGCCTGGTCCTC[C/T]TCTGCTAAGCCTCCT	328967
rs29677805	snp	C/T	0.5	0	intron-variant	Arhgef37	GRCm38.p3	18:61524931	ACGATAATGTCAGTG[C/T]GTCCCTGCCCCTTTC	328967
rs29678217	snp	A/C/T	0.5	0	downstream-variant-500B	Arhgef37	GRCm38.p3	18:61493623	TATGGAAGTGTAAGC[A/C/T]GAATAAACCCTTTCC	328967
rs29721172	snp	C/T	0.444444	0.157135	utr-variant-3-prime	Arhgef37	GRCm38.p3	18:61494108	GAAATCACACCATCC[C/T]TCACCTACCCAGAGC	328967
rs29724734	snp	C/G	0.375	0.216506	intron-variant	Arhgef37	GRCm38.p3	18:61522149	AAATCCCAACACCCA[C/G]GTGAAAGCTCACAAC	328967
rs29724778	snp	C/T	0.387812	0.208586	intron-variant	Arhgef37	GRCm38.p3	18:61507847	AGCATATACTGACCA[C/T]CACTCCATCAGCTGG	328967
rs29726428	snp	A/G	0.408163	0.193609	intron-variant	Arhgef37	Mm_Celera	18:61502203	TCTGTCAGATGCCGC[A/G]TGGAAAACCTCAGAA	328967
rs29726904	snp	A/C	0.375	0.216506	intron-variant	Arhgef37	Mm_Celera	18:61520786	ACAAAACAAAACAAA[A/C]CAAAAAAACAACAAC	328967
rs29736832	snp	A/G	0.459184	0.136902	intron-variant	Arhgef37	GRCm38.p3	18:61522864	CATCAAGTTCGGCGT[A/G]TCCAGCATGGAAGGA	328967
rs29768417	snp	A/G	0.444444	0.157135	intron-variant	Arhgef37	GRCm38.p3	18:61501241	ATAAAAATCTATCTC[A/G]AACACACACACACAC	328967
rs29769211	snp	C/T	0.444444	0.157135	intron-variant	Arhgef37	GRCm38.p3	18:61508154	GGCGGTAGCACACAC[C/T]CTTAATCCCAGCACT	328967
rs29810875	snp	A/C	0.444444	0.157135	intron-variant	Arhgef37	GRCm38.p3	18:61518906	ACGTTTAATATTTCT[A/C]TACTGTCACTCCATA	328967
rs29819092	snp	A/T	0.5	0	intron-variant, utr-variant-5-prime	Arhgef37	Mm_Celera	18:61512206	AATGGGCTTTTTTTT[A/T]ATTTCCTTTTTTTTA	328967
rs29823325	snp	A/G	0.444444	0.157135	downstream-variant-500B, utr-variant-3-prime	Arhgef37	GRCm38.p3	18:61493790	ACACTGTTGGCTTGG[A/G]CATGAGGGGTGGCAC	328967
rs29860691	snp	A/G	0.444444	0.157135	intron-variant	Arhgef37	GRCm38.p3	18:61508622	TCCCTGAAGCACCCC[A/G]AAACGCAAGTCCCTA	328967
rs29864862	snp	G/T	0.375	0.216506	intron-variant	Arhgef37	Mm_Celera	18:61511862	GCAACTCACACAATT[G/T]TTAAAAGAATTTAAT	328967
rs29868105	snp	A/G	0.5	0	intron-variant	Arhgef37	GRCm38.p3	18:61517691	AAAGAGGGAGGGAAG[A/G]AGAGAGGGAGGAATG	328967
rs29874985	snp	C/T	0.375	0.216506	intron-variant	Arhgef37	Mm_Celera	18:61502415	CTCCTGGGGTCAGGC[C/T]GTTCTGCTCTTCTCT	328967
rs29876081	snp	A/G	0.32	0.24	intron-variant	Arhgef37	Mm_Celera	18:61528189	TAAATAAATAAATAA[A/G]TAAATAAATAAAATT	328967
rs29878560	snp	C/T	0.459184	0.136902	intron-variant	Arhgef37	GRCm38.p3	18:61506697	AAACAGTATAAACTG[C/T]ATGTGGTGGCACAGG	328967
rs29883182	snp	C/T	0.444444	0.157135	intron-variant	Arhgef37	GRCm38.p3	18:61508520	CACATATCAGGCAAG[C/T]ACCTGGTCAGCAGAA	328967
rs29912625	snp	A/G	0.444444	0.157135	intron-variant	Arhgef37	GRCm38.p3	18:61518807	AGACCCCCGGATGAT[A/G]TGAAAGGAGTCACAG	328967
rs29923398	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Arhgef37	GRCm38.p3	18:61514018	GCTAGAAAATGCATC[C/T]CCATCCTTTCTCCTT	328967
rs29923874	snp	A/C/G	0.5	0	intron-variant	Arhgef37	GRCm38.p3	18:61519769	GTTTCTCTGGATAGC[A/C/G]CTAGCTGTTCTGGAA	328967
rs29953315	snp	C/T	0.444444	0.157135	intron-variant	Arhgef37	GRCm38.p3	18:61514781	ACTGACAGCAACACT[C/T]TCCTAAAGCCATTCT	328967
rs29958745	snp	G/T	0.375	0.216506	upstream-variant-2KB, utr-variant-5-prime	Arhgef37	GRCm38.p3	18:61536775	ACAATGGGTTTCTTC[G/T]GTGCTGCGAGCAGAA	328967
rs29966227	snp	A/G	0.46875	0.121031	intron-variant	Arhgef37	Mm_Celera	18:61521990	TGAGATCATTCTGAC[A/G]CTTGGTACCACGGTC	328967
rs29983239	snp	A/G	0.387812	0.208586	utr-variant-3-prime	Arhgef37	GRCm38.p3	18:61494561	GCAACATTCATCCTA[A/G]ACATGAGAGAGGAAA	328967
rs30014687	snp	A/G	0.375	0.216506	intron-variant, utr-variant-5-prime	Arhgef37	GRCm38.p3	18:61511976	TCCATCCACATGTCG[A/G]AAGCAGAGAGAGAGA	328967
rs30014723	snp	C/T	0.359862	0.224567	utr-variant-3-prime	Arhgef37	GRCm38.p3	18:61493929	CCTCATGACATACAT[C/T]CTTACCACATCCCAC	328967
rs30017012	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	Arhgef37	Mm_Celera	18:61512258	TATGAGTACACCATC[C/G]CTCTCTTCAGACACC	328967
rs30021032	snp	A/C	0.387812	0.208586	synonymous-codon	Arhgef37	GRCm38.p3	18:61505705	GAGCTGAAGGTCCCT[A/C]GCTAGGCTGCAGTAC	328967
rs30026050	snp	C/G	0.444444	0.157135	intron-variant	Arhgef37	Mm_Celera	18:61498554	CCCCAGCTCTCATCA[C/G]GACCAGGGCTGCCTT	328967
rs30055894	snp	A/G	0.387812	0.208586	intron-variant	Arhgef37	GRCm38.p3	18:61506529	CTGTCTGTAAGTAAA[A/G]TCATATGTGCGAGGG	328967
rs30066078	snp	A/G	0.5	0	downstream-variant-500B, utr-variant-3-prime	Arhgef37	GRCm38.p3	18:61493658	AACTGCTTCTTGGTC[A/G]TGATGTTTGTGCAGG	328967
rs30107545	snp	A/G	0.375	0.216506	intron-variant	Arhgef37	GRCm38.p3	18:61522150	AATCCCAACACCCAG[A/G]TGAAAGCTCACAACC	328967
rs30112387	snp	C/G	0.32	0.24	intron-variant	Arhgef37	GRCm38.p3	18:61536375	GCCTGACCCCAACAA[C/G]AACAACCTCGCGCAC	328967
rs30112832	snp	C/T	0.375	0.216506	intron-variant	Arhgef37	GRCm38.p3	18:61516722	TCTGAATTTTTGACA[C/T]TTGAGGCTATCTATT	328967
rs30116970	snp	C/T	0.375	0.216506	intron-variant	Arhgef37	GRCm38.p3	18:61532267	CACCCACCGGGATAA[C/T]GGTGTCATGACTGTT	328967
rs30125744	snp	A/G	0.444444	0.157135	intron-variant	Arhgef37	GRCm38.p3	18:61524517	TCGGAGGCCCAGAAT[A/G]AGGAAAAGTTCACTT	328967
rs30155333	snp	C/T	0.444444	0.157135	intron-variant	Arhgef37	Mm_Celera	18:61500800	TACTAACAAAGAGTC[C/T]GGATTATGAACCAGG	328967
rs30160882	snp	A/G	0.484429	0.0868505	intron-variant	Arhgef37	Mm_Celera	18:61496518	TTCATAACCCATACC[A/G]GTCATCCCTTTAAAG	328967
rs30165104	snp	A/T	0.5	0	intron-variant	Arhgef37	GRCm38.p3	18:61510405	TAAAGAGATGACTGC[A/T]TTTTTTTTTTTTAAT	328967
rs30175119	snp	A/G	0.5	0	downstream-variant-500B	Arhgef37	GRCm38.p3	18:61493607	TGGTGATGAACAGCA[A/G]TATGGAAGTGTAAGC	328967
rs30205003	snp	A/G	0.375	0.216506	intron-variant	Arhgef37	Mm_Celera	18:61523085	TTTCAGCCGGCTCCA[A/G]CTCCTTCCTTGTCTG	328967
rs30214853	snp	G/T	0.375	0.216506	intron-variant	Arhgef37	GRCm38.p3	18:61522151	ATCCCAACACCCAGG[G/T]GAAAGCTCACAACCA	328967
rs30223266	snp	A/G	0.375	0.216506	intron-variant	Arhgef37	Mm_Celera	18:61521474	AGACTAGGTGTGGGT[A/G]GGGGGGTGGGGTGTC	328967
rs30227705	snp	C/T	0.304688	0.243945	intron-variant	Arhgef37	GRCm38.p3	18:61503446	TAGCGAGTCAGATGA[C/T]GACAGGGAAGCACAG	328967
rs30258066	snp	A/G	0.5	0	downstream-variant-500B	Arhgef37	GRCm38.p3	18:61493609	GTGATGAACAGCAGT[A/G]TGGAAGTGTAAGCCG	328967
rs30268529	snp	A/T	0.375	0.216506	intron-variant	Arhgef37	Mm_Celera	18:61520837	CAAAAACAAAAGACA[A/T]GGGGCTGGAGAGATG	328967
rs30269548	snp	C/T	0.32	0.24	intron-variant	Arhgef37	Mm_Celera	18:61516101	ACTCATGGATGAAAT[C/T]GTCAAGAAATGTGAA	328967
rs30271517	snp	C/T	0.375	0.216506	intron-variant	Arhgef37	Mm_Celera	18:61503571	GAACTGCCACCTAGT[C/T]CCTCCCATACCAACT	328967
rs30307935	snp	C/T	0.375	0.216506	synonymous-codon, utr-variant-5-prime, intron-variant	Arhgef37	GRCm38.p3	18:61508790	CTTGGTAATCCTCTG[C/T]AGAGGGATCACAAGG	328967
rs36268503	snp	C/T	0.444444	0.157135	intron-variant	Arhgef37	Mm_Celera	18:61495569	AGGGAGTTAGCTTAT[C/T]CGTCCAGACCCGTTT	328967
rs36338755	snp	A/G	0.408163	0.193609	intron-variant	Arhgef37	Mm_Celera	18:61524188	GTGTCTGAACAATGC[A/G]AGAGGTCAAACAACA	328967
rs36350403	snp	A/C	0.345679	0.230967	intron-variant	Arhgef37	Mm_Celera	18:61521040	ACAAAACAAAAAAAA[A/C]ATTACTTTGTTCCTG	328967
rs36360580	snp	C/T	0.32	0.24	intron-variant	Arhgef37	Mm_Celera	18:61535162	TTACTGAACGTATGT[C/T]ACGGTATCTTTGACT	328967
rs36369173	snp	C/T	0.260355	0.249785	intron-variant	Arhgef37	Mm_Celera	18:61506861	GTCCAGGCTCACTTG[C/T]TTCCTAGCTGTGTGG	328967
rs36401607	snp	C/T	0.391111	0.206368	intron-variant	Arhgef37	Mm_Celera	18:61497311	GGAAAGAGTTCTCAG[C/T]ACACGTGGCCCTATC	328967
rs36413021	snp	A/G	0.32	0.24	intron-variant	Arhgef37	GRCm38.p3	18:61525786	ATCGTGTCTTCCTGT[A/G]ACATACTTACCATGA	328967
rs36467043	snp	C/T	0.260355	0.249785	intron-variant	Arhgef37	Mm_Celera	18:61506223	ATCTGTAATTCCAGT[C/T]CCAAAAGACCGTTGA	328967
rs36527865	snp	A/G	0.35503	0.226867	intron-variant	Arhgef37	Mm_Celera	18:61521593	TAACCCTGGCCTGAG[A/G]ACAGCCACAGACCCT	328967
rs36533534	snp	A/C	0.391111	0.206368	intron-variant	Arhgef37	Mm_Celera	18:61505787	CTGAGGAAAACCTGA[A/C]TCCAGGGCCAACAGA	328967
rs36572894	snp	A/G	0.231111	0.249285	intron-variant	Arhgef37	Mm_Celera	18:61498010	TCACAAGGAGGTGAT[A/G]GAAGGAGCAGTCACT	328967
rs36584354	snp	G/T	0.21875	0.248039	intron-variant	Arhgef37	Mm_Celera	18:61535627	CAGCCGTGTTTGATC[G/T]GATTATCGGCATCAG	328967
rs36587536	snp	A/G	0.396694	0.202437	intron-variant	Arhgef37	Mm_Celera	18:61501461	ACATGAGGGAGGGAA[A/G]CTTCAGCACACTGCA	328967
rs36588789	snp	G/T	0.444444	0.157135	utr-variant-5-prime, intron-variant	Arhgef37	Mm_Celera	18:61536445	CGGCATCCTGTCGCC[G/T]TCGCCGGGCTGGACT	328967
rs36603689	snp	C/T	0.497041	0.0383476	intron-variant	Arhgef37	Mm_Celera	18:61495672	AAGTTCTCTATGGCT[C/T]GTTGTCATCCCCTAC	328967
rs36607470	snp	C/T	0.473373	0.11227	intron-variant	Arhgef37	Mm_Celera	18:61503617	TCCACCGCAAGTTTG[C/T]GCGTGGTGGTCTGTG	328967
rs36617035	snp	C/T	0.391111	0.206368	intron-variant	Arhgef37	Mm_Celera	18:61497836	GCTCCTATTCATCAC[C/T]GTGACTCTCATTTAG	328967
rs36619272	snp	C/T	0.426035	0.177515	intron-variant	Arhgef37	Mm_Celera	18:61526048	ACCCAGATTTCTTCA[C/T]TGGGCTCAGCTAAGT	328967
rs36619731	snp	A/G	0.497041	0.0383476	intron-variant	Arhgef37	Mm_Celera	18:61506165	ACTGTTCTTGCAGTG[A/G]ACCTGGGTTTGGTTC	328967
rs36622126	snp	G/T	0.444444	0.157135	intron-variant	Arhgef37	Mm_Celera	18:61498505	TGAAGTTCATCCCTG[G/T]GCCCTCTAGTGGCCG	328967
rs36636431	snp	C/T	0.132653	0.220748	intron-variant	Arhgef37	Mm_Celera	18:61526330	GTGATTTTTCTAAGG[C/T]TCCAGGACCATCTTT	328967
rs36650883	snp	A/G	0.132653	0.220748	intron-variant	Arhgef37	Mm_Celera	18:61498674	CCGCTTCCCAGGTGG[A/G]TAGAGTCTTCACACC	328967
rs36672336	snp	A/G	0.391111	0.206368	intron-variant	Arhgef37	Mm_Celera	18:61495250	TACTGTATGGCTGAC[A/G]TAGTTCTAACACTTT	328967
rs36722802	snp	C/T	0.48	0.0979796	intron-variant	Arhgef37	Mm_Celera	18:61496048	GGGACCCTTTGTAGT[C/T]CCTGAGATGTATTAT	328967
rs36745451	snp	C/G/T	0.391111	0.206368	intron-variant	Arhgef37	GRCm38.p3	18:61500250	CCAGGCCTTAGCCAT[C/G/T]TGGAATCCTCAGAGG	328967
rs36750549	snp	C/T	0.165289	0.235211	intron-variant	Arhgef37	Mm_Celera	18:61520355	GCACCTGTCTTTTAA[C/T]TGTGATCCACCATAC	328967
rs36766174	snp	G/T	0.473373	0.11227	intron-variant	Arhgef37	Mm_Celera	18:61495246	TAATTACTGTATGGC[G/T]GACATAGTTCTAACA	328967
rs36772770	snp	C/G	0.260355	0.249785	intron-variant	Arhgef37	Mm_Celera	18:61506393	ATGGGCTTGGCCTTT[C/G]GACCCTGCAGGGCTC	328967
rs36825180	snp	A/G	0.459184	0.136902	intron-variant	Arhgef37	Mm_Celera	18:61502650	CAGTCTTTGCCTTGC[A/G]AGTCTTGAATCACAG	328967

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