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
rs31031084	snp	C/G	0.444444	0.157135	intron-variant, utr-variant-5-prime	Atg16l2	GRCm38.p3	7:101301789	CCTCGGGAACCGTGA[C/G]GGCGCCGCTGCCCTG	73683
rs31050069	snp	A/G	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101297622	TACACACACTGACCC[A/G]GCCTCCACAGCACTA	73683
rs31054881	snp	G/T	0.401235	0.199068	intron-variant	Atg16l2	GRCm38.p3	7:101298545	AACACTGCAATATCA[G/T]GATGGTTACATGATA	73683
rs31092392	snp	G/T	0.415225	0.187619	intron-variant	Atg16l2	GRCm38.p3	7:101300380	GGGAATATCTGTATC[G/T]GGCAAAGCCTCATCA	73683
rs31096715	snp	C/T	0.5	0	intron-variant	Atg16l2	GRCm38.p3	7:101299522	GGGCCCCAGCACCTA[C/T]ATTAAAGAACCTGGC	73683
rs31137827	snp	C/G	0.444444	0.157135	intron-variant, utr-variant-5-prime	Atg16l2	GRCm38.p3	7:101301625	ACGGCCTGAAAGAAG[C/G]ACTCGACAAAACCAT	73683
rs31153367	snp	C/T	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101296465	CACATCCTAGGGAAG[C/T]TCCCCAATACTAGAG	73683
rs31154377	snp	A/G	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101294935	ACCTGGGGCAGAATG[A/G]AGAGACACACTGAGA	73683
rs31154515	snp	A/C	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101299202	AAAGCTTGAGAAGCC[A/C]TTCGCTTTCTCTTGG	73683
rs31156061	snp	A/G	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101298186	TTCTTTCTCCTCAGG[A/G]CCTGAGGAGCAAGCC	73683
rs31197356	snp	C/T	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101299307	GGTCCAGACCTTGGA[C/T]CCCCATCAGTGACAC	73683
rs31199870	snp	C/T	0.429688	0.173817	upstream-variant-2KB	Atg16l2	GRCm38.p3	7:101302555	AAAGGACTCTTAAGC[C/T]CTGGAAAGAACAAGT	73683
rs31201903	snp	A/T	0.444444	0.157135	utr-variant-3-prime, nc-transcript-variant	Atg16l2	GRCm38.p3	7:101288432	AGCTGTGTTACCTTG[A/T]ATGACAATCTTTTCT	73683
rs31274721	snp	A/G	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101297931	GCCAGACTCAGTCCT[A/G]GAGCCCTGGGTTGAG	73683
rs31285149	snp	A/C	0.444444	0.157135	utr-variant-3-prime, nc-transcript-variant	Atg16l2	GRCm38.p3	7:101288600	AGAAAAAAAAAAAAA[A/C]CAAAATAAAACAAAA	73683
rs31290730	snp	A/C	0.444444	0.157135	intron-variant	Atg16l2	GRCm38.p3	7:101292064	CTGCAAATCTTAAGT[A/C]ATAACCCTTTAACCC	73683
rs31360757	snp	A/G	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101290536	GCTAGAGTGCCTCCC[A/G]GGACTTTGCTTGCAC	73683
rs31429827	snp	C/T	0.375	0.216506	utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant	Atg16l2	GRCm38.p3	7:101302066	CGCAAAGCTCCAGCC[C/T]GAGCAGGGGGGCGGA	73683
rs31434310	snp	A/G	0.401235	0.199068	intron-variant	Atg16l2	GRCm38.p3	7:101298456	TAGCGGTAGAAACAG[A/G]TTAGTGGTTGCCAAG	73683
rs31453644	snp	A/G	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101295762	CCCATCTGGTCTCAA[A/G]TGTGAACACACTTTG	73683
rs31470059	snp	A/C	0.444444	0.157135	intron-variant, nc-transcript-variant	Atg16l2	GRCm38.p3	7:101292211	GGAAAGGCCCTGGAC[A/C]TCACTAGATCAGGTC	73683
rs31489276	snp	A/G	0.375	0.216506	intron-variant	Atg16l2	Mm_Celera	7:101294740	AATAAATCTTAAAAA[A/G]AAAAAAAAAGATGCA	73683
rs31492844	snp	C/G	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101298993	CAACATTCTCAGACC[C/G]GACCCTGCTTACCTC	73683
rs31514042	snp	A/G	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101297793	GGGGCTGCAAGGGAT[A/G]TGAGTTCTAGTTCCC	73683
rs31527299	snp	C/T	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101297323	TTCCTGACAAGGAAG[C/T]CCAGGCTGAGATAAG	73683
rs31540414	snp	C/T	0.387812	0.208586	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Atg16l2	GRCm38.p3	7:101302167	TCGGGGAGATCTGGA[C/T]ACCTCAAAGCAGGTG	73683
rs31585777	snp	A/T	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101298258	GCCTGGAGAGGGGGA[A/T]CCTGTGCAGCCAGGT	73683
rs31596351	snp	A/G/T	0.444444	0.157135	intron-variant, utr-variant-5-prime	Atg16l2	GRCm38.p3	7:101301723	ACCAGAGCTGGAAAC[A/G/T]GCAGGCAAGCCAATG	73683
rs31596368	snp	C/T	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101296322	GTGATAAACGCTAGC[C/T]GCTAAGTATTGGCTT	73683
rs31597989	snp	A/G	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101294819	AGGAAGCCTTACAGG[A/G]GGTGCCGGTCCCTTC	73683
rs31647995	snp	A/G	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101295983	TTGGAAGTAGAGAAT[A/G]GGGTAACACTGCCTC	73683
rs31663137	snp	C/G	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101296711	TACACCTTTTAACCA[C/G]GCGAGTCCAGATTGC	73683
rs31680040	snp	A/T	0.375	0.216506	downstream-variant-500B	Atg16l2	GRCm38.p3	7:101286138	AGAAAAAGAAAAATT[A/T]AAAAAACAAGAAAAT	73683
rs31751928	snp	C/T	0.444444	0.157135	intron-variant, synonymous-codon, utr-variant-3-prime, downstream-variant-500B	Atg16l2	GRCm38.p3	7:101290017	CATCCAACCAGCAGG[C/T]GGTTTGAGAAGCCTC	73683
rs31757586	snp	A/G	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101297432	TCCTTTATTTTCTCG[A/G]TGCACCTGCAGTAGA	73683
rs31772081	snp	C/G	0.387812	0.208586	intron-variant	Atg16l2	GRCm38.p3	7:101298624	GCACACTGGGGAGAG[C/G]CCCTCAAATGTCTTC	73683
rs31785638	snp	A/G	0.391111	0.206368	utr-variant-3-prime, nc-transcript-variant	Atg16l2	GRCm38.p3	7:101286333	ATCTGGCTGCAATGA[A/G]CCTCTGCATTTATTT	73683
rs31785640	snp	A/G	0.359862	0.224567	utr-variant-3-prime, nc-transcript-variant	Atg16l2	GRCm38.p3	7:101286778	GAACAACCTTCTGCC[A/G]TGCATGGATTTGCCT	73683
rs31785642	snp	G/T	0.415225	0.187619	utr-variant-3-prime, nc-transcript-variant	Atg16l2	GRCm38.p3	7:101286807	CTGCCATAATCTAAG[G/T]CTCAGCCCTCAACTT	73683
rs31786714	snp	C/T	0.401235	0.199068	utr-variant-3-prime, nc-transcript-variant	Atg16l2	GRCm38.p3	7:101287018	TCTAGAGACTGTCTA[C/T]AGGGCACTGGAGGGG	73683
rs31786717	snp	A/G	0.124444	0.216185	utr-variant-3-prime, nc-transcript-variant	Atg16l2	Mm_Celera	7:101287236	CATAACAGCCTGGAA[A/G]ACATTATGACTTCCC	73683
rs31786720	snp	A/G	0.444444	0.157135	intron-variant, downstream-variant-500B	Atg16l2	GRCm38.p3	7:101290142	AACATGGAAGTTTGC[A/G]TGTGGAAGTTTTCAG	73683
rs31787646	snp	A/G	0.432133	0.171253	intron-variant	Atg16l2	GRCm38.p3	7:101298896	CTCTGCAGCTATAAC[A/G]TCATGGAGGACTGAC	73683
rs31787649	snp	A/G	0.124444	0.216185	intron-variant	Atg16l2	Mm_Celera	7:101300531	GTTCACCTCTGCCAG[A/G]GACAAAGTCTGGACC	73683
rs31787651	snp	A/G	0.124444	0.216185	intron-variant	Atg16l2	Mm_Celera	7:101300551	AAGTCTGGACCCAGA[A/G]CATGTTGAAATAAAC	73683
rs31789036	snp	A/C	0.297521	0.245442	intron-variant, utr-variant-5-prime	Atg16l2	Mm_Celera	7:101301729	GCTGGAAACAGCAGG[A/C]AAGCCAATGCGGAGA	73683
rs31789039	snp	A/G	0.408163	0.193609	intron-variant, utr-variant-5-prime	Atg16l2	GRCm38.p3	7:101301771	GGTTCCAAGACGCAA[A/G]GCCCTCGGGAACCGT	73683
rs31789043	snp	A/C	0.124444	0.216185	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Atg16l2	Mm_Celera	7:101302198	CTGCTGCGGCCCAGC[A/C]AAAACCCTCAGTCCC	73683
rs31789878	snp	A/G	0.444444	0.157135	upstream-variant-2KB	Atg16l2	GRCm38.p3	7:101302571	CTGGAAAGAACAAGT[A/G]GACATGGTCTGATGA	73683
rs31789881	snp	A/C	0.336735	0.234472	upstream-variant-2KB	Atg16l2	GRCm38.p3	7:101302727	TCCGTGGGAGGAGCA[A/C]GATTTAGAGGTCCAG	73683
rs31790714	snp	C/G	0.124444	0.216185	upstream-variant-2KB	Atg16l2	GRCm38.p3	7:101302793	CGTTTATCTGGAAAA[C/G]CCCAGGCTCAGAGGA	73683
rs31790717	snp	C/G	0.444444	0.157135	upstream-variant-2KB	Atg16l2	GRCm38.p3	7:101303706	CCTGCTGGAAGTCTG[C/G]CTCTGCTCACACATC	73683
rs31810988	snp	A/T	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101296361	ACACATTATCTCTAC[A/T]CGTGTCTAGTGACCT	73683
rs31854185	snp	A/G	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101297442	TCTCGGTGCACCTGC[A/G]GTAGATATTTAACCT	73683
rs31900407	snp	C/T	0.444444	0.157135	intron-variant	Atg16l2	GRCm38.p3	7:101295030	AAGCTCATGCTCACT[C/T]GCTCAAGGCAGGAAC	73683
rs31904496	snp	C/T	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101298815	TGAATGAAGAATCCC[C/T]GAAAGTAGATTTGTG	73683
rs31922750	snp	A/C	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101298810	AGGAGTGAATGAAGA[A/C]TCCCTGAAAGTAGAT	73683
rs31995850	snp	C/G	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101299206	CTTGAGAAGCCATTC[C/G]CTTTCTCTTGGGGTA	73683
rs32047806	snp	A/G	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101299227	TCTTGGGGTAGTTGG[A/G]AGCCAACCAGAGAAC	73683
rs32047914	snp	G/T	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101297585	ATTAGCTGGCACTTG[G/T]CATGCTTTGCCCCAA	73683
rs32076995	snp	C/T	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101296616	CTGAAGGAGGTGCTT[C/T]GCAGATGGGGCACCA	73683
rs32085620	snp	A/G	0.444444	0.157135	synonymous-codon, nc-transcript-variant	Atg16l2	GRCm38.p3	7:101290704	AACCCGGCCCTGCAC[A/G]GGGATGACCTGGATG	73683
rs32089014	snp	A/C/G	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101298994	AACATTCTCAGACCG[A/C/G]ACCCTGCTTACCTCA	73683
rs32093326	snp	G/T	0.444444	0.157135	utr-variant-3-prime, nc-transcript-variant	Atg16l2	GRCm38.p3	7:101287407	TAAAATTAAAAAAAT[G/T]TTTGAACAGTCTTAT	73683
rs32107396	snp	A/G	0.5	0	utr-variant-3-prime, nc-transcript-variant	Atg16l2	GRCm38.p3	7:101288222	AAAAAGTTGTATAAA[A/G]AGAGAGGATGTGGGT	73683
rs32134687	snp	C/T	0.444444	0.157135	intron-variant	Atg16l2	GRCm38.p3	7:101295067	TTGACTCCTTGCAGA[C/T]TAGGAGAGGATGACA	73683
rs32175381	snp	A/G	0.444444	0.157135	utr-variant-3-prime, nc-transcript-variant	Atg16l2	GRCm38.p3	7:101287693	TGGCTCTTCCTCAAG[A/G]GAACTGAAGGGGCAG	73683
rs32283208	snp	G/T	0.375	0.216506	intron-variant	Atg16l2	Mm_Celera	7:101291649	CAGGAGCCACTACAT[G/T]TGGTGGCTGTAAGGT	73683
rs32316975	snp	A/G	0.444444	0.157135	utr-variant-3-prime, nc-transcript-variant	Atg16l2	GRCm38.p3	7:101289108	GCCAGATTTCCACAA[A/G]TTCTGAGCTATTACA	73683
rs32327244	snp	G/T	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101296739	TGCCTCCCCAGGGGC[G/T]TGGCCCAGAGTTTTC	73683
rs32327866	snp	A/C	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101297435	TTTATTTTCTCGGTG[A/C]ACCTGCAGTAGATAT	73683
rs32427383	snp	A/C	0.375	0.216506	intron-variant	Atg16l2	GRCm38.p3	7:101297902	ACTTAGAACAAGACC[A/C]CGGGAGAGCAGGAGC	73683
rs32476970	snp	C/G	0.444444	0.157135	utr-variant-3-prime, nc-transcript-variant	Atg16l2	GRCm38.p3	7:101287601	CCCTTTCATATAGTT[C/G]TGCTTTGTGATGCTA	73683
rs32502309	snp	A/G	0.375	0.216506	intron-variant, nc-transcript-variant	Atg16l2	GRCm38.p3	7:101292344	ATGCTGTGGGACAAA[A/G]TCTCCTTACTGAGGG	73683
rs45867447	snp	C/T			intron-variant	Atg16l2	Mm_Celera	7:101293027	ACGGCACATAGATTT[C/T]TGTTTGAGGCCAGCC	73683
rs46567132	snp	C/T			intron-variant	Atg16l2	GRCm38.p3	7:101293636	GGGTCTCTGCAAACC[C/T]GAGTTTCAAACCTGT	73683
rs46805561	snp	C/T			upstream-variant-2KB	Atg16l2	GRCm38.p3	7:101303901	GTATGTGTGTGTGCA[C/T]GTGCACGAGTGCAGG	73683
rs46821685	snp	A/G			intron-variant	Atg16l2	GRCm38.p3	7:101294268	CTTTTTTGAGCTTCA[A/G]TTTCCCAACTGATCA	73683
rs46885605	snp	A/G			intron-variant	Atg16l2	GRCm38.p3	7:101294779	CAGGTACCAAAGGAT[A/G]GACAGAGCAAGGCTG	73683
rs46958136	snp	A/G			intron-variant	Atg16l2	Mm_Celera	7:101294200	ATGGATACAGGAAGC[A/G]TTACGGATGGCATTA	73683
rs47302408	snp	A/G			intron-variant	Atg16l2	GRCm38.p3	7:101294643	CAGCAACCACATGGT[A/G]GCTCACAACCGCCCA	73683
rs47663285	snp	C/T			intron-variant	Atg16l2	GRCm38.p3	7:101293562	TCCTCATACATGGCT[C/T]CTTGTGCCCACTCCC	73683
rs47709370	snp	C/T			upstream-variant-2KB	Atg16l2	Mm_Celera	7:101302639	CTCAGCGATAGGGTT[C/T]TTGCTAACCCTGCGC	73683
rs48067240	snp	A/G			intron-variant	Atg16l2	GRCm38.p3	7:101294016	AGAAAAGCATCCAGC[A/G]AAGCCTGCTGACATG	73683
rs48786271	snp	G/T			intron-variant	Atg16l2	Mm_Celera	7:101293528	AAAAAAGTGGGCAGG[G/T]CTGGCTGCACCCCAT	73683
rs48798267	snp	C/T			intron-variant	Atg16l2	GRCm38.p3	7:101294116	ACAGTAAACAAGGTC[C/T]GCAACGCAGCCTGAC	73683
rs48846671	snp	A/G			upstream-variant-2KB	Atg16l2	GRCm38.p3	7:101302501	AGTGGGGGTTTATGA[A/G]GGACCAACTAAGACC	73683
rs48913943	snp	A/T			upstream-variant-2KB	Atg16l2	GRCm38.p3	7:101304124	TTGAATGGTAGGGGA[A/T]TCAAAGAGTATGGTG	73683
rs49434386	snp	C/T			intron-variant	Atg16l2	GRCm38.p3	7:101294318	GCCCTCAGTCCCCTA[C/T]GAACAAGGACAGAGC	73683
rs49708089	snp	G/T			upstream-variant-2KB	Atg16l2	GRCm38.p3	7:101303831	TAGGAAGTCATGTTG[G/T]GGCAGGTTTTTTAAT	73683
rs49895241	snp	C/G			intron-variant	Atg16l2	GRCm38.p3	7:101294176	AGCCCAGCAGACACA[C/G]ACAGGGTGATGGATA	73683
rs50130768	snp	C/T			intron-variant	Atg16l2	GRCm38.p3	7:101293630	CTCTGAGGGTCTCTG[C/T]AAACCTGAGTTTCAA	73683
rs50424494	snp	A/G			intron-variant	Atg16l2	Mm_Celera	7:101294741	AATAAATCTTAAAAA[A/G]AAAAAAAAGATGCAC	73683
rs50539513	snp	A/T			intron-variant	Atg16l2	GRCm38.p3	7:101293847	ATTCCTATCAGCACC[A/T]CAGGCATGTGGCCCA	73683
rs50791501	snp	G/T			intron-variant	Atg16l2	GRCm38.p3	7:101300306	CTGGGATGGCTGCAG[G/T]AGCCCAGGGGTCTTG	73683
rs50851308	snp	A/G			intron-variant	Atg16l2	GRCm38.p3	7:101293542	GGCTGGCTGCACCCC[A/G]TTCTTCCTCATACAT	73683
rs52040021	snp	C/T			intron-variant	Atg16l2	GRCm38.p3	7:101290875	CTGACAAAACTACTG[C/T]CCCTTCCCACTGTGG	73683
rs211795054	snp	C/G			intron-variant	Atg16l2	Mm_Celera	7:101292860	CATACTGCAGGCCAG[C/G]CTTCCAGAGTTGGTG	73683
rs211812030	snp	A/G			upstream-variant-2KB	Atg16l2	Mm_Celera	7:101304248	GCTATGGAGTCATCC[A/G]CTGGGGCATGGGGGG	73683
rs211812186	snp	C/T			intron-variant	Atg16l2	Mm_Celera	7:101292050	CCCAAATAACCACTC[C/T]GCAAATCTTAAGTAA	73683

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