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
rs891655	snp	A/G	0.0681886	0.171594	intron-variant	ATG16L2	GRCh38.p7	11:72817928	AATTCAGCAAACACA[A/G]GAGTACCCGTCACTG	89849
rs891657	snp	G/T	0.0150606	0.0854603	intron-variant	ATG16L2	GRCh38.p7	11:72829180	CCTGTGAGCTAACTT[G/T]ACAGATGAGGAAACA	89849
rs919600	snp	C/T	0.00676609	0.0577691	intron-variant	ATG16L2	GRCh38.p7	11:72818748	TATAGCAACTGTCAA[C/T]AGATGTTGAGAGAAT	89849
rs1045315	snp	C/G	0	0	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841516	ACCAGCCTCCCAGCA[C/G]CCCCTACCCCAGCCC	89849
rs1045372	snp	A/C	0	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72836863	ATGGAATCCAGCACC[A/C]CAGTGCACAGGTCAG	89849
rs1062909	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838452	CAGTCCCTAAATTAC[G/T]GATCATGTGCACTCG	89849
rs1062910	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838373	TCTTCAAGTGGCTTT[G/T]GCTCATCTGATTGAG	89849
rs1126205	snp	A/C	0.379942	0.213577	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812749	TCCCTTTAGAACTGG[A/C]GGACTCTTGGGTGCT	89849
rs1298094	snp	A/C	0	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838251	AGTCCAATTTTTCCC[A/C]ATAAGGTTTCACTTT	89849
rs1320730	snp	A/T	0	0	intron-variant	ATG16L2	GRCh38.p7	11:72817678	CTTGTTTTAGGCTTT[A/T]CATGTAGCATCACTT	89849
rs1801886	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838230	AAATTGGACTGCCCT[G/T]AATTTAGCACCAATT	89849
rs1807188	snp	A/G	0.00335007	0.0407899	intron-variant	ATG16L2	GRCh38.p7	11:72817223	ATAGGTTGGGGCTCA[A/G]AGTTGGGAGGTGCTT	89849
rs1808621	snp	C/T	0.00676609	0.0577691	intron-variant	ATG16L2	GRCh38.p7	11:72817364	GGGTGGTGGTGCACG[C/T]TCCAGGAGGCTGAGG	89849
rs1864651	snp	G/T	0.0108365	0.0728068	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821524	GCGTCCCTGTGCAAG[G/T]TCCCAAACCTGTGTG	89849
rs1864652	snp	G/T	0.000271186	0.0116413	utr-variant-5-prime, intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821576	AAGGGGGCGGGCAGG[G/T]GAGCAGCCGACTCCC	89849
rs2282613	snp	C/T	0.495351	0.0479864	intron-variant	ATG16L2	GRCh38.p7	11:72819151	AATGAGGTGGGCTGT[C/T]CTTCCTGTCTTCCTG	89849
rs2303969	snp	A/G	0.477684	0.103247	intron-variant	ATG16L2	GRCh38.p7	11:72825227	GTCTGCACAGGCACC[A/G]GTAAGAGGGCCCGTG	89849
rs3214595	in-del	-/C	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72825523	TCTATCTGGAATATT[-/C]TGTGGGCAGTGACTA	89849
rs3765638	snp	A/G	0.331874	0.236213	intron-variant	ATG16L2	GRCh38.p7	11:72826027	CTCCAGCCCAGGCCC[A/G]CAGAACAGACCCAGC	89849
rs3814729	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838441	AATATACTGTACGAG[C/T]GCACATGATCAGTAA	89849
rs3862793	snp	C/T	0.00716266	0.059414	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827096	GTCTTGGGAGGACAC[C/T]GGGTTCTGGGCCTCA	89849
rs3862794	snp	A/G	0.38821	0.208322	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827555	ATAAAAGTGGTAACT[A/G]AATGGAAAAAGGTAC	89849
rs3862795	snp	A/G	0.00755907	0.0610114	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827661	GCAAAGCTAGAGGCC[A/G]GGCGTGGTGGCTCAT	89849
rs4245436	snp	C/T	0.00159617	0.0282053	intron-variant	ATG16L2	GRCh38.p7	11:72816279	GCCACCGCGCCCGGC[C/T]GGGGATTATTTTTAA	89849
rs4944014	snp	C/T	0.403334	0.197456	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72816135	AGGCGCCTGCCACCA[C/T]GCCTGGCTAATTTTT	89849
rs4944806	snp	A/G	0.00557542	0.0525036	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822666	CCCCCATGTGGTCGG[A/G]GCCCACGAGACACCT	89849
rs4944808	snp	A/G	0.00279162	0.0372561	intron-variant	ATG16L2	GRCh38.p7	11:72834218	GAAAAACAACTTCAC[A/G]ATGAACAAAATAAAT	89849
rs6592491	snp	A/G	0.00676609	0.0577691	intron-variant	ATG16L2	GRCh38.p7	11:72831487	TCTAGCCTGGGCAAC[A/G]AGAGTGAAACTCCAT	89849
rs6592492	snp	A/G	0.00557542	0.0525036	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837551	ACAGGAGCGGACAGC[A/G]GACAGTCAGCACCTG	89849
rs7110183	snp	C/T	0.221439	0.248363	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839990	gaggaagaaagcaaa[C/T]gaggcaaatgtagAG	89849
rs7120156	snp	A/C	0.0770498	0.180522	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821088	ACTCACATTCCCCTG[A/C]CCAGCCTGGAGGGTG	89849
rs7924575	snp	C/T	0	0	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815140	GCTGGTGGATGCTGG[C/T]TGAGCCCAGCGAAGT	89849
rs7936074	snp	C/T	0.0130921	0.0798413	intron-variant	ATG16L2	GRCh38.p7	11:72831642	AGCAGCCACCAGGGG[C/T]CACCAGCTGCCTAGT	89849
rs7939267	snp	A/G	0.0792508	0.182605	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815291	GGAAGTCTAACCACA[A/G]TCCCTGCGGCTCTCT	89849
rs7940683	snp	C/T	0.0444908	0.142359	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842035	CAAGATCGGCAAACA[C/T]GTTCCTTCTTCCTCT	89849
rs7950432	snp	A/C	0.00716266	0.059414	intron-variant	ATG16L2	GRCh38.p7	11:72832256	GAGCCCTTCTCTCCC[A/C]CAAAACCTTCCCTTC	89849
rs10751215	snp	C/T	0.489142	0.0728777	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815042	CTCAGGCTCTGCCGC[C/T]GACAGGCGACGCTGG	89849
rs10751216	snp	C/T	0.489259	0.0724914	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815078	GCTTATGGAACACCT[C/T]CCTGTCAGCCTACCC	89849
rs10898880	snp	A/C	0.48955	0.071525	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814066	AGCACCAGCGGCTCT[A/C]GAACTCGGCCCGGGC	89849
rs10898881	snp	A/G	0.492037	0.0625946	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815973	GCTGGGGAAGTTGGG[A/G]TTATTTATTTATTTA	89849
rs10898882	snp	C/G	0.00716266	0.059414	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827899	GATTGCGCCACTGCC[C/G]TCCAGCCTGGGCGAC	89849
rs10898883	snp	A/C	0.0955749	0.196603	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72827957	AAACCAAAACCAAAA[A/C]CAAAACAAAACAAAA	89849
rs11235600	snp	C/T			utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814494	GCGCGCTGGAAACGC[C/T]ACATCGTGCGGCAGC	89849
rs11235601	snp	G/T	0.426478	0.186327	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814897	CGGGCAGTCCCCGGG[G/T]TAGGGGCTTGATCAG	89849
rs11235602	snp	C/T	0.00716266	0.059414	intron-variant	ATG16L2	GRCh38.p7	11:72820427	TAATCTGTTTTCCAC[C/T]TCTACTACTTGAATT	89849
rs11235603	snp	C/T	0.00179026	0.0298651	utr-variant-5-prime, intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821663	GCCCACCTGTCCGCC[C/T]CCAGATGGCCTACCA	89849
rs11235604	snp	C/T	0.0136909	0.0815967	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822491	AGGGCCAAGCAGGCG[C/T]GGGTGTCCCAGGAGC	89849
rs11235605	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72834725	gtagctgggattaca[C/G]gtacccaccaccaca	89849
rs11430316	in-del	-/T	0.00676609	0.0577691	intron-variant	ATG16L2	GRCh38.p7	11:72834897	CCATCATTCCATTCC[-/T]TTTACAATTGAGGAT	89849
rs11600601	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72819877	cagcctcccgagtag[C/T]tgggactacaggcgc	89849
rs11602724	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72819898	ctacaggcgcccgcc[A/C]ccatgcccggctaat	89849
rs11604683	snp	C/T	0.172674	0.237741	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827501	TGGCTCTTGGTCCAA[C/T]GCTGGACTCCGCCTG	89849
rs11605818	snp	A/G	0.0119091	0.0762411	intron-variant	ATG16L2	GRCh38.p7	11:72835207	TTTCACTGGCAGGGA[A/G]GTCAGAAGACGGAAA	89849
rs11824212	snp	C/T	0.0825414	0.185628	intron-variant	ATG16L2	GRCh38.p7	11:72831337	catagtgaaaccttg[C/T]ctctactaaaaatac	89849
rs12271465	snp	C/T	0.0138799	0.0821421	intron-variant	ATG16L2	GRCh38.p7	11:72819186	TGCCCCCCAGTCGTT[C/T]TCACACATGCTGGAA	89849
rs12293084	snp	A/G	0.0126979	0.078662	intron-variant	ATG16L2	GRCh38.p7	11:72829233	TACCCAGGTCCAGCA[A/G]TCGGGGCAGAGCCAG	89849
rs12794689	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72825122	GCAGGGGTCCAGGCA[G/T]AGGTGAGAACACCTG	89849
rs12808532	snp	C/T	0.0246875	0.108325	splice-acceptor-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840960	CATGAAGGCTTTTTT[C/T]TAAGGGAGAAAACCA	89849
rs34006101	in-del	-/G			intron-variant	ATG16L2	GRCh38.p7	11:72835798	TGTTCCCCAGACTGG[-/G]AGTGTAATGGCACAA	89849
rs34065651	in-del	-/A			intron-variant	ATG16L2	GRCh38.p7	11:72830523	GAGACACACAAAAAA[-/A]CCTTAGTGCAGCCTC	89849
rs34132493	in-del	-/A			intron-variant	ATG16L2	GRCh38.p7	11:72825834	CTGGAGAGGGGGTGT[-/A]CCTGGGGAGTCAGAG	89849
rs34325800	in-del	-/T			intron-variant	ATG16L2	GRCh38.p7	11:72817400	TAATATTTGTATTTT[-/T]AGTAGAGACGGGGTT	89849
rs34384997	in-del	-/A			intron-variant	ATG16L2	GRCh38.p7	11:72830597	CCTGGTCTTCCCGAA[-/A]GGGCTGGGATTACAG	89849
rs34683629	in-del	-/CATT/CATTCATT	0	0	intron-variant	ATG16L2	GRCh38.p7	11:72830803	ATTCATTCATTCATT[-/CATT/CATTCATT]TACTCATTTAGAGAT	89849
rs34696027	snp	G/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823011	CTGAGCCCCACCCCA[G/T]AGGCTGCCAGGGTCT	89849
rs34732465	in-del	-/T	0.499968	0.00399348	intron-variant	ATG16L2	GRCh38.p7	11:72833932	AATTTTTTTTTTTTT[-/T]CAGGAAAATATTCCC	89849
rs34789461	in-del	-/A			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837346	TACTTTTGGTCAAAA[-/A]TCCCATGGGGACATT	89849
rs34976675	in-del	-/G			intron-variant	ATG16L2	GRCh38.p7	11:72831684	TTCCCGTTTCCAGGG[-/G]ACACATGGCTGGGGA	89849
rs35220889	in-del	-/C			intron-variant	ATG16L2	GRCh38.p7	11:72833072	CAGATGCCCCTATCC[-/C]TGTGCTCCTACTGCC	89849
rs35333793	in-del	-/C			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842134	TAAAGGCTGTTTCCC[-/C]TGTGATGAACTAAGT	89849
rs35388270	in-del	-/G			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815115	GGGGGCATCAGGGGG[-/G]CCCCGGGCTGCTGGT	89849
rs35407315	in-del	-/GTCT	0.319856	0.240042	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828155	AGCTTTCAAATCAAA[-/GTCT]GTCTAAGTTCCTCGA	89849
rs35499071	in-del	-/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840268	ACTCAATACATATTT[-/T]GCTGAATGAATGAAG	89849
rs35634761	in-del	-/G			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828243	CCCCAGCGATCCAGG[-/G]CCCTGGGGTTCCTCC	89849
rs35740958	snp	A/G	0.00118199	0.0242817	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826801	CCGGACAGTGAAGGA[A/G]TGGGACCTCGGCCGT	89849
rs35868740	snp	C/T	0.00199481	0.0315187	intron-variant	ATG16L2	GRCh38.p7	11:72819814	ACAGTCGCGTCATCT[C/T]GGCTCGCTGCAACCT	89849
rs56060052	snp	G/T	0.020002	0.0979842	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836507	CGTATTTCTTTTTTT[G/T]CCCATGGGAAAAGCA	89849
rs56071001	snp	A/C	0.105924	0.204309	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827939	TGTCTCAAAACAAAA[A/C]CAAAACCAAAACCAA	89849
rs56088156	snp	C/T	0.00914312	0.0669923	intron-variant	ATG16L2	GRCh38.p7	11:72832523	GCGGGAAGGCTGTTC[C/T]TCCCTCCAGCCTCTT	89849
rs56148078	snp	A/C	0.275999	0.248644	intron-variant	ATG16L2	GRCh38.p7	11:72818313	TCTTGGCTTCTCTTT[A/C]ACCATGCTCTCCTGG	89849
rs57674996	in-del	-/ATCT			utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829594	TTTTTATCTCTATCT[-/ATCT]CCTCACTTTTTCTCC	89849
rs58682117	snp	C/T	0.34526	0.23114	intron-variant	ATG16L2	GRCh38.p7	11:72819955	TTTCACCATGTTAGC[C/T]AGGATGGTTTTGATC	89849
rs58718333	snp	A/G			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813592	TCTGGCCCTGAGTCA[A/G]GATGCTGGGGTGCTG	89849
rs59059938	snp	C/T	0.0825414	0.185628	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840778	CATCCTTGTTTGGCA[C/T]AGTCAGTAACAACAC	89849
rs59348649	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72816237	CGCCCGCCTCGGCCT[C/T]CCAGAGCGCTGGGAA	89849
rs59748827	in-del	-/A			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841364	AAAAAAAAAAAAAAA[-/A]GCAAATGCAGTTTTT	89849
rs60091261	in-del	-/A			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841341	GAGACTCTGTCTCCA[-/A]AAAAAAAAAAAAAAA	89849
rs61049260	snp	C/T	0.0387552	0.1337	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841137	CCCACCACTGCACTC[C/T]AGCCTGGGTGACAGA	89849
rs61348171	snp	A/C			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815568	GAGAGATCTGGAGGG[A/C]TGAAATCAGACTGAA	89849
rs61738587	snp	A/G	0.00314142	0.0395075	missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825333	AGGTCAATGCTGTTC[A/G]TTTTGGCCCCAACAG	89849
rs61894254	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814947	GCAGTGAAAGAACGC[A/G]GGACTTGTCCAGAGC	89849
rs61894255	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72834601	TTTTTTTTTTTTTTG[G/T]AGACAGAGTCTTGCT	89849
rs61894256	snp	A/G	0.5	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837464	TGATTTCTTAACCAA[A/G]GAAAAAAAAAAAAAA	89849
rs67634043	in-del	-/ATTC			intron-variant	ATG16L2	GRCh38.p7	11:72830789	TTTCCTTGCTATTCA[-/ATTC]TTCATTCATTTACTC	89849
rs71062791	in-del	-/CTCACCACCACCTCTC	0	0	intron-variant	ATG16L2	GRCh38.p7	11:72835437	TCACCACGAACTCTT[-/CTCACCACCACCTCTC]CTCACCACCACCTCT	89849
rs71477744	snp	C/G	0.00517822	0.0506191	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823911	GATCTGGGTCACCCT[C/G]GTCTCCTGATCTTGG	89849
rs71477745	snp	C/T	0.00478085	0.0486577	intron-variant	ATG16L2	GRCh38.p7	11:72834129	GAAACTTAAAAGTTG[C/T]AGGATTTGGGGATAA	89849
rs71477746	snp	A/G	0.5	0	intron-variant	ATG16L2	GRCh38.p7	11:72835439	AGGTGGTGGTGAGGA[A/G]AGGTGGTGGTGAGAA	89849
rs71477747	snp	C/T	0.5	0	intron-variant	ATG16L2	GRCh38.p7	11:72835833	AGCTCACCGCAACCT[C/T]TGCCTCGCAGGTTCA	89849
rs72969813	snp	C/G	0.0293117	0.117459	intron-variant	ATG16L2	GRCh38.p7	11:72828842	TGTGTGTGCCCTCCC[C/G]TCTGACCCCCCGTTT	89849

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