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
rs6233379	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90975241	CCTCATCGGTTACTA[C/T]GTAGTAATGTAGTAT	66795
rs6235066	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90975583	tattttctttattta[C/T]atttcaaatgttatc	66795
rs6235598	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90975676	acccacccttgcctc[C/T]ccatcctggcattcc	66795
rs6257910	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:91028608	gtttttgctatcctc[A/G]gtttttCCCTATCTC	66795
rs6258402	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:91094734	GTGTACATTTGGCTC[C/T]GTTTCCGTAACTGTT	66795
rs6258859	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:91094816	CTTTTAACCCTTCTG[C/T]GTATGGGGAAAACTG	66795
rs6258901	snp	A/C	0.5	0	intron-variant	Atg10	Mm_Celera	13:91094844	CTGGTTTTCTTTAAG[A/C]GCTTTTGAGTGAACA	66795
rs6272767	snp	C/T	0.21875	0.248039	intron-variant	Atg10	Mm_Celera	13:91135311	ATCATTTGCACTTAT[C/T]GTCATATCTATACTT	66795
rs6273924	snp	A/C	0.290657	0.246672	intron-variant	Atg10	Mm_Celera	13:91135504	GGGCAGTGGGCATAT[A/C]GGAAGACAGGCTTCT	66795
rs6274417	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90956800	aatgctgaacttctg[C/T]agcataaaatgctct	66795
rs6274497	snp	A/G	0.290657	0.246672	intron-variant	Atg10	Mm_Celera	13:91135607	CTTCAGGGAGTTTAC[A/G]ATGGGTTGTTTTCGT	66795
rs6274536	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:90956859	gtatcattcttcttc[A/G]aatcatggaccctga	66795
rs6275013	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90956919	ttttgaactcatgct[C/T]ttagagttctttccc	66795
rs6275085	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:90956965	gtcctgaaggtcaca[A/G]cnttctaccattttg	66795
rs6275086	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:90956967	cctgaaggtcacanc[A/G]ttctaccattttgct	66795
rs6276675	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90957249	gcaggaaccatgtca[C/T]gctgtcccttccatg	66795
rs6288319	snp	C/T	0.456747	0.140554	intron-variant	Atg10	GRCm38.p3	13:91135890	CCTCTGCAAAAGAAA[C/T]GGAATGTCAGTAATG	66795
rs6288428	snp	A/G	0.359862	0.224567	intron-variant	Atg10	Mm_Celera	13:91135969	GTAATTCCCTTGCAA[A/G]TGTTCGCTGGTAATT	66795
rs6310977	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90997902	aaacttgtatagcca[C/T]gatggaaatcaatat	66795
rs6311488	snp	A/C	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90997999	ACCAAAGGACCCTCC[A/C]TCTTACCACAAGGAC	66795
rs29221652	snp	G/T	0.459184	0.136902	intron-variant	Atg10	GRCm38.p3	13:91005214	GTTGAAAGATGAGAA[G/T]TACTTCAATTCTAAT	66795
rs29223118	snp	C/G	0.265928	0.249492	intron-variant	Atg10, Gm35245	Mm_Celera	13:90964373	TGTTACTAAATCACA[C/G]TGTATACCACAATGA	66795
rs29223712	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91151894	GTGATAAGAAGGAAG[A/G]GATAAGGGTTCCACT	66795
rs29223880	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90946542	GTAAAAATCATATGG[C/T]ATTGACATTAAAACA	66795
rs29223928	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90947539	GGAGACAGGAATGGG[C/T]GGGATCTGGTGGAGG	66795
rs29224249	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90981652	GGAAAGTGAAGGCTA[C/T]AGGAGAAACAGATCC	66795
rs29224276	snp	A/C	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91040670	TGGGATGATATCATT[A/C]ACTATGAAGTCTGCT	66795
rs29224525	snp	C/G/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91158149	GAAGCCCAAGGTCAG[C/G/T]CCGCTCAACTGAGAT	66795
rs29224904	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:91063802	TTTCCTCTTTCTCCA[C/T]ATCCTCTCCAGCATT	66795
rs29225051	snp	C/T	0.304688	0.243945	intron-variant	Atg10	Mm_Celera	13:91095025	GCACAGAGTAGATGG[C/T]AGACGCAGGTCAGAG	66795
rs29225083	snp	C/G	0.391111	0.206368	intron-variant	Atg10	GRCm38.p3	13:91139177	TGTCAGACTCTGACA[C/G]TAGTCAGCCTCCGAA	66795
rs29225142	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91216163	GCTGAAGTGTCACTT[A/G]AGTCTGTGAGCTTAA	66795
rs29225399	snp	C/T	0.304688	0.243945	intron-variant	Atg10	Mm_Celera	13:90976489	TCCAGTTTTATAGAG[C/T]TGTTTTTCAATTGTT	66795
rs29225573	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Atg10	GRCm38.p3	13:91166320	CACTATATCTTAAAA[A/G]CAGTCCCTGAAAGAA	66795
rs29225585	snp	A/T	0.492188	0.0620098	intron-variant	Atg10	GRCm38.p3	13:91082048	TAGAGAAACTGTTGA[A/T]GGGTGTCTATTTGGC	66795
rs29225657	snp	A/G	0.391111	0.206368	intron-variant	Atg10	Mm_Celera	13:90957418	TCAGTAGGTCCTGTA[A/G]AACTGAAAGACACAA	66795
rs29225975	snp	A/G	0.32	0.24	intron-variant, nc-transcript-variant	Atg10, Gm35245	Mm_Celera	13:90970428	GTAGAAATTTCGGAG[A/G]ATCTCTCTCTGCCTA	66795
rs29226115	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90988447	AACGCTACGTGGACA[A/G]TACTTCATACCAAAC	66795
rs29226151	snp	A/C	0.304688	0.243945	intron-variant	Atg10	Mm_Celera	13:91112501	TTGAATTTATATGTT[A/C]ATTTTACTGACTTCT	66795
rs29226156	snp	A/G	0.444444	0.157135	intron-variant, downstream-variant-500B	Atg10	Mm_Celera	13:90937002	GCTGCCTATATTCAA[A/G]TCCCAGTCCCACCCC	66795
rs29227050	snp	A/T	0.277778	0.248452	intron-variant	Atg10, Gm35245	Mm_Celera	13:90963682	CGCGTAAGTCAAAGG[A/T]CACAGTTTCTTCTCC	66795
rs29227270	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91076829	TTCCCACAAGCTCAC[A/G]TTTGCTTAATACATG	66795
rs29227384	snp	A/G	0.48	0.0979796	intron-variant	Atg10	Mm_Celera	13:90947017	TGTGGATCAAGGGGA[A/G]CACTCCTCCATAAAC	66795
rs29227835	snp	C/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91180209	CAGCTACAAGGATAA[C/T]AGGCAACTACTGAGT	66795
rs29228090	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:90942523	GAATAAAAAGACACT[A/G]ACTACAATATGTACT	66795
rs29228170	snp	A/G	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91058706	CAGGCAAATGGATGG[A/G]ACTAGAAAATATCAT	66795
rs29228232	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91119307	TGTTCACAAAGGCAA[C/T]ACAGGTCTGGGGTTC	66795
rs29228426	snp	G/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91126647	ACTTCTACCTTGACT[G/T]AGCAGCACAGTGGAG	66795
rs29228656	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:91080301	TTAACAGTGGTTCAA[A/G]CAATATGAACTAACC	66795
rs29228722	snp	C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91198885	CATAACACACACACA[C/T]ATATATATATGAAAT	66795
rs29228833	snp	A/G	0.42	0.183303	intron-variant	Atg10	GRCm38.p3	13:91036575	TTGGGTGCATTTTAC[A/G]TTCTATATCCTGGCT	66795
rs29228900	snp	A/G	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91075970	AATTCTGACACTGAT[A/G]TGTATGTGTCCTGGA	66795
rs29229243	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91017273	AGCATGACACTACCC[A/G]GTCAAAATTCTACCA	66795
rs29229362	snp	C/T	0.48	0.0979796	intron-variant	Atg10	GRCm38.p3	13:91034934	ACACATATACACACA[C/T]ACACACAGATGTGTG	66795
rs29229411	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90982808	CAAGGCCCTGGAAGC[A/G]CAAAGGGTTTTGGGG	66795
rs29229439	snp	A/T	0.32	0.24	intron-variant	Atg10	GRCm38.p3	13:91169760	AGCAAGTTTGCAAGG[A/T]TGCATGGGGAGAGTT	66795
rs29229742	snp	C/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91063273	GAGAGGGGTTGAAAG[C/T]GTTGAACATTTCCTG	66795
rs29230000	snp	C/T	0.387812	0.208586	intron-variant	Atg10	GRCm38.p3	13:91049176	CTTAATTTTATTGTG[C/T]CTTTATAAGCAGAAA	66795
rs29230101	snp	A/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90947272	GCATAATGAAGTATT[A/T]CTCAGCTGTGAAAAA	66795
rs29230296	snp	C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91114320	AGGAACTGCTCTGAC[C/T]CTTCCTAGCCAAGGT	66795
rs29231074	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91042289	TTATGGGATGTGGAA[C/T]AGTCGGCAGGTGGAC	66795
rs29231153	snp	A/G	0.493827	0.0552116	intron-variant	Atg10	GRCm38.p3	13:91112478	CACATAAAAATACTC[A/G]TCCTAGTTTGAATTT	66795
rs29231456	snp	A/C	0.391111	0.206368	intron-variant	Atg10	GRCm38.p3	13:91156008	CTTGGAAGCTTGCTA[A/C]TTATGACTCAATTCT	66795
rs29231458	snp	A/T	0.277778	0.248452	intron-variant, nc-transcript-variant	Atg10, Gm35245	Mm_Celera	13:90971296	ACAATAGAGTTAATT[A/T]TAAATTTGGCAAATT	66795
rs29231487	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91185798	ACAAGCAAAACACCA[C/T]CCAACACAACTGACT	66795
rs29231694	snp	C/T	0.387812	0.208586	intron-variant	Atg10	GRCm38.p3	13:91048040	GCAAGAGAGCCCATA[C/T]AGCCTCTTTAAAAGG	66795
rs29231947	snp	C/G	0.444444	0.157135	intron-variant, downstream-variant-500B	Atg10	Mm_Celera	13:90936863	GTGATCCGAGGTTTT[C/G]TGAAGATCTCTCACC	66795
rs29232019	snp	A/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91159412	AAGCATTTATTAGAT[A/T]TATATGCTATGTGTG	66795
rs29233172	snp	C/T	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91099556	TGCCATTCCCTCACA[C/T]CACCCATCTTCCTGC	66795
rs29233258	snp	A/C	0.290657	0.246672	intron-variant	Atg10	Mm_Celera	13:90981468	TGGTCATCACACTGA[A/C]GAAAGCCTCAATGCT	66795
rs29233368	snp	C/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91123028	AGAGTCCAAGAGAGC[C/T]CAGAAAACAATGCAG	66795
rs29233674	snp	A/G	0.391111	0.206368	intron-variant	Atg10	GRCm38.p3	13:91156097	TTAATATCATTCCTG[A/G]CTGGAGAGTAAACTA	66795
rs29233868	snp	A/C	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91113413	ATGCATAAGACATGA[A/C]CAGGTAAAGTCACAC	66795
rs29233891	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91122866	ATATATATATATATA[C/T]ATACATATATATATA	66795
rs29234038	snp	C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91206761	AGGGAAATACTTGAG[C/T]ATATCAGGCTTTTTT	66795
rs29234441	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91181059	ATGGGCTTCATTCTA[C/T]GTGTTTAATGCCAGC	66795
rs29234960	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91219573	GAGTTGGGGGTGTGT[C/T]CAGGAATAAAAGGGC	66795
rs29235103	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91179708	ACCAGGAAGAAGCAC[A/G]TGTGCCAAGCTGCCA	66795
rs29235466	snp	C/T	0.429688	0.173817	intron-variant	Atg10	Mm_Celera	13:91193314	TGCTTCCTCGGAGTG[C/T]ATGCACAGCTGCCAG	66795
rs29235936	snp	G/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:91120403	AATTTTATTTGTAAT[G/T]CATTTTTTACACTCC	66795
rs29236062	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90948688	TGACTCTGATTATGG[A/G]GTATAGCGGTTAAGG	66795
rs29236321	snp	A/G	0.497778	0.0332592	intron-variant	Atg10	GRCm38.p3	13:91157747	AATACCATAAATAAA[A/G]ATCCAAATTACTTCT	66795
rs29236478	snp	A/T	0.375	0.216506	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Atg10	Mm_Celera	13:91224202	CCAGGGTATCTGCAC[A/T]CCCTTCCCCACACGC	66795
rs29236575	snp	A/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91067082	CATAGAAAAAGATAA[A/G]GAAGGACACTTCATA	66795
rs29236811	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90949921	CAGACCAAGTAGGTG[C/T]CTTAGTTAAGGTTAT	66795
rs29237019	snp	A/G	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91179717	AAGCACATGTGCCAA[A/G]CTGCCACACTCGGAA	66795
rs29237125	snp	G/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91071985	GAAGCCCTAGACAAC[G/T]TAGCAAATTACAATA	66795
rs29237126	snp	A/C	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91000313	AAGGGCTGCCTTGAT[A/C]ATGGTATCTGTTTAC	66795
rs29237303	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91192357	TCCCAGTGTAATCAA[A/G]TTACTATGTTGTGGA	66795
rs29237570	snp	A/C	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90972715	CAATGGCTGCCCCCC[A/C]AAATATTCTCAAAAG	66795
rs29237584	snp	C/T	0.465374	0.126941	intron-variant	Atg10	GRCm38.p3	13:91077831	GCCATTATCTCTTCT[C/T]CCTTTCATACTGACT	66795
rs29237789	snp	C/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91184584	GGGTCAGCAAGCTGA[C/G]CTGTTCTCATGATAC	66795
rs29238088	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:91059911	GCTGGCCCTGGTAGT[A/G]TGAGCACAGGAGAGA	66795
rs29238337	snp	A/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91155913	AATTTAAAGTTTTTT[A/T]AAAAATTAGAGAAAG	66795
rs29238578	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:90947235	TCAACAGAAGAATGA[A/G]TAAATACACATTGGT	66795
rs29238833	snp	A/C	0.401235	0.199068	intron-variant	Atg10, Gm35245	Mm_Celera	13:90966163	TAAATGAAGCTGCCA[A/C]GTTACTCTGTTCAGT	66795
rs29239293	snp	C/T	0.492188	0.0620098	intron-variant	Atg10	GRCm38.p3	13:91116392	CCATGATGGTAACAT[C/T]AGAAACAAAGACCTC	66795
rs29239393	snp	C/T	0.336735	0.234472	intron-variant	Atg10, Gm35245	Mm_Celera	13:90967206	ATAATAATTAAAAGA[C/T]TTAATGCTCAGGTTG	66795
rs29239454	snp	C/T	0.277778	0.248452	intron-variant	Atg10	Mm_Celera	13:91009944	GTTCTGAAGAAGCAG[C/T]GGCAACCTATAAAGC	66795
rs29239943	snp	G/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91201095	GATAGAAATAAAAGA[G/T]TAGCTTTGAAGACAT	66795

Full records

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