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
rs1620	snp	A/G	0.0318976	0.122194	intron-variant	FCHSD2	GRCh38.p7	11:73009815	catgctttttttctt[A/G]ctgttttttgaattc	9873
rs152997	snp	A/G	0.0988009	0.199095	intron-variant	FCHSD2	GRCh38.p7	11:72909380	ggtggaggttgtagc[A/G]agccgagatcacgcc	9873
rs429574	snp	A/G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72909351	GCTCAATGTTGCCCA[A/G/T]GCTGGAGTGCAGTGG	9873
rs479093	snp	C/T	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:72974529	AGCACTgctgttcaa[C/T]agagttttctaagat	9873
rs493315	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72970906	AAGGCAATACCAAGA[A/G]GCCAAGTGCAGAAGC	9873
rs494413	snp	C/T	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:72977628	ctgccgaagcgagca[C/T]GCtctcacaccagtt	9873
rs508532	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72981137	TACTGTACATTAACT[A/C]ATTTTCTTCCTCATG	9873
rs509597	snp	C/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72975511	taggagagaagattt[C/G]gaaatgttctcaaca	9873
rs537980	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72980199	CCCCCTCTTCAAACC[C/T]CAAACTTACCCCTTC	9873
rs555773	snp	A/G	0.0988009	0.199095	intron-variant	FCHSD2	GRCh38.p7	11:72973166	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA	9873
rs560258	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72973637	GGGGTCACCTGGGAG[A/G]TTTCCACTGTACTGA	9873
rs573529	snp	G/T	0.137187	0.223099	intron-variant	FCHSD2	GRCh38.p7	11:72976504	aggctggtctcaaac[G/T]cttggactcaagtga	9873
rs593301	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72980296	AAGCAGTGTTGAAAC[C/T]GCTGCACTGGTTTCT	9873
rs593753	snp	C/T	0.297128	0.245518	intron-variant	FCHSD2	GRCh38.p7	11:72980395	CAGATTATCCAGTTA[C/T]GGGGGCTCATCAGAG	9873
rs640283	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72971714	TCTTCCCCAGAATCT[C/T]CAGATAAGAATGCAG	9873
rs658164	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72977623	atgtgctgccgaagc[A/G]agcatgctctcacac	9873
rs671766	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72972713	ACCAATGTAGCAGGG[A/G]AAGAATCTATTACCC	9873
rs724673	snp	C/T	0.333952	0.235483	intron-variant	FCHSD2	GRCh38.p7	11:73084663	CCCATGCCAGTAATC[C/T]CAATGCTTTGGGAGG	9873
rs898384	snp	C/T	0.0854556	0.188216	intron-variant	FCHSD2	GRCh38.p7	11:72985604	CTTCTATTATTTCCA[C/T]CATTAAAAGTACTTC	9873
rs975261	snp	A/G	0.0869089	0.189476	intron-variant	FCHSD2	GRCh38.p7	11:72953443	TGTTTTACAAGGAGT[A/G]CTAGTGTCAAATAAG	9873
rs994305	snp	A/G	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72886273	GTATTTCCCAATACT[A/G]AACTCACATCTCCTT	9873
rs1025411	snp	C/G	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72955104	gttagcagtctgtga[C/G]acctgacgctctcca	9873
rs1031706	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72975044	TTTTTGGAATTAATG[C/T]TTAGCCAGAAAAACC	9873
rs1045315	snp	C/G	0	0	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841516	ACCAGCCTCCCAGCA[C/G]CCCCTACCCCAGCCC	9873
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	9873
rs1062909	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838452	CAGTCCCTAAATTAC[G/T]GATCATGTGCACTCG	9873
rs1062910	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838373	TCTTCAAGTGGCTTT[G/T]GCTCATCTGATTGAG	9873
rs1065100	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73078633	TTTTTTTTTTTTATC[A/G]GAATAGTTGTTATTT	9873
rs1290092	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72857649	cagcctggccaacat[A/G]gtgaaacccccgtct	9873
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	9873
rs1299173	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72890947	TTCATTCTACAATTT[G/T]GCTGCTTTCTATATT	9873
rs1367698	snp	C/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72863831	CCTTATCAGTACTTA[C/G]TATAGTCAGTCTTTT	9873
rs1367699	snp	A/C	0.225005	0.248747	intron-variant	FCHSD2	GRCh38.p7	11:72863755	TTTTAATTTCCATTT[A/C]TCTGATAATGTTGAT	9873
rs1380574	snp	C/T	0.097727	0.198275	intron-variant	FCHSD2	GRCh38.p7	11:73085166	CCTTAAACCTAAAGA[C/T]TCATGCTTATTCAAG	9873
rs1380575	snp	C/T	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:73085383	TAACCATTTTGGAAC[C/T]AGGAGTCAACTGAAA	9873
rs1460035	snp	A/G	0.0284301	0.115788	intron-variant	FCHSD2	GRCh38.p7	11:73015315	ATAATACTTATTTTA[A/G]AAAAATATATGTGTT	9873
rs1612659	snp	A/G	0.42574	0.177808	intron-variant	FCHSD2	GRCh38.p7	11:73124258	gtccccccatcccac[A/G]ataggccctggtgtg	9873
rs1614447	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72890881	AAAAACAAACTTTAT[G/T]GAGATAATTAGGaat	9873
rs1619988	snp	C/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73128398	CACCACTACCTTTTT[C/G/T]GTTTGTTGGCAAGGA	9873
rs1783598	snp	A/G	0.342806	0.232136	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140418	TAGGAAGACCTAGAC[A/G]TGGATTGAGCTTGTG	9873
rs1785207	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72898275	ATAAAATGTAACTCT[C/T]CTGATGATTTTCATA	9873
rs1785208	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72897337	CAGACACAACTATCC[C/T]TTTTTTTTTTTTTTT	9873
rs1785209	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72882282	cctgtcttttattac[A/C]agtaaaaaaattagc	9873
rs1785215	snp	A/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72890838	AGAATTTAGAGAGAA[A/T]TAAAATAGTTTTGTG	9873
rs1785216	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72888504	ATCCGTCTCATTCTT[G/T]GCCTTCACATCCTGC	9873
rs1785217	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72920955	CAAGAATATATATAC[A/C]AGAGGCATTCAGGAT	9873
rs1785218	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72851980	ctcctgggctcaagc[A/C]atcttcctgcctcag	9873
rs1785219	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72852002	CTGCCTCAGCCTCCC[A/G]AATAGATGGGACTAT	9873
rs1790279	snp	A/C	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72977390	ACAATCAACAAAGTG[A/C]AGAGACAGCCCATGG	9873
rs1790285	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72924821	TACATAATTACATGG[A/G]AATCATAGTAATAAT	9873
rs1790286	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72918344	aattgaaaaagaaga[A/G]ttaaaattacctctc	9873
rs1791053	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73134430	caagctggagcacag[G/T]ggtgtgatcatggct	9873
rs1791054	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73134317	atgcctggctaattt[G/T]gtattttttgtagag	9873
rs1801886	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838230	AAATTGGACTGCCCT[G/T]AATTTAGCACCAATT	9873
rs1835644	snp	C/G	0.0988009	0.199095	intron-variant	FCHSD2	GRCh38.p7	11:72948162	AAATTTGCCAGGTCT[C/G]GTGGCACATGCCTGT	9873
rs1982038	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72844500	TCCCTGACAGCAGCA[A/G]TCCACCAGCATCAGC	9873
rs1982585	snp	C/T	0.499053	0.0217445	intron-variant	FCHSD2	GRCh38.p7	11:73071429	GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	9873
rs1989449	snp	C/T	0.282105	0.24793	intron-variant	FCHSD2	GRCh38.p7	11:73084945	CCTCCTTCTTACTCT[C/T]ATGTCTTTGGTCTTT	9873
rs2003368	snp	A/G	0.377582	0.214995	intron-variant	FCHSD2	GRCh38.p7	11:73129061	ACATGGTGAAATCTC[A/G]TCTCTACTAAAAATA	9873
rs2032351	snp	C/G/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73045152	ttttttcatgtgttt[C/G/T]ttggctgcataaatg	9873
rs2043156	snp	C/G	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:72874614	AGAATGTAGTGAATA[C/G]TTCTCTCTTTTCTGC	9873
rs2060071	snp	A/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72932315	CCAACTCATTTCCAC[A/T]CTGCAGCTAGGAGGA	9873
rs2060072	snp	C/T	0.0588605	0.161139	intron-variant	FCHSD2	GRCh38.p7	11:72896192	ACTAAATTTCTGATG[C/T]ATGATCTTTCCCTGT	9873
rs2060073	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72857572	acacacctgtagtcc[C/T]agctactccggaggc	9873
rs2187494	snp	A/G	0.443195	0.158668	intron-variant	FCHSD2	GRCh38.p7	11:73094558	TATTTATTCTTAAAT[A/G]GAGTAAAGCTCAGTA	9873
rs2276379	snp	A/G	0.499053	0.0217445	intron-variant	FCHSD2	GRCh38.p7	11:73047308	CTTCCCTATCATTTA[A/G]GTATGTAGCTTCTAC	9873
rs2365906	snp	A/G	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72854437	TCTGTCTACCTATCT[A/G]TCTATCTGGTTAgag	9873
rs2365907	snp	G/T	0.00756178	0.0610554	intron-variant	FCHSD2	GRCh38.p7	11:72878553	ctgtgatagcttgtt[G/T]tactaggaagaaagt	9873
rs2365908	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72880991	atttttatggctgag[A/G]ctttaaggccacagg	9873
rs2365909	snp	A/C	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72881074	cagcaaaggaaacaa[A/C]agagttaacagatga	9873
rs2366252	snp	C/G	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73034956	GCAGGTGACATTTAT[C/G]CTATAGTACTTTAGC	9873
rs2366256	snp	A/G	0.369754	0.219451	intron-variant	FCHSD2	GRCh38.p7	11:73109675	ACTTTTTCCCTTTCC[A/G]CTTTGGATGCTCTTT	9873
rs2446746	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72981874	TGGTCCTAGCTACAT[A/G]GGAGGCTGAGGCAAG	9873
rs2886599	snp	A/C	0.190205	0.242744	intron-variant	FCHSD2	GRCh38.p7	11:73010226	TTCATTCAATGAATT[A/C]TTCCATTACAGAATT	9873
rs3018279	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73131701	ttttttttttttgga[A/G]acatagtctgggttg	9873
rs3018280	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73131691	ttggaaacatagtct[G/T]ggttggtggcctaaa	9873
rs3018281	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73131550	tgcccAGATATTTTT[G/T]GTAGTAAtttttatt	9873
rs3039677	in-del	-/CT	0.0341408	0.126114	intron-variant	FCHSD2	GRCh38.p7	11:72985692	GAGAAAGTCCTGGGA[-/CT]CTCTGCCCTGTATGA	9873
rs3040733	in-del	-/TATTA			intron-variant	FCHSD2	GRCh38.p7	11:73033994	GGTATTAAAATTGTC[-/TATTA]TATTTTCATGATTTC	9873
rs3133221	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73128012	GAAAAAGACCATTTC[A/C]AAAAAAAAAAAAAAA	9873
rs3207374	snp	A/G	0.0429648	0.14013	intron-variant	FCHSD2	GRCh38.p7	11:72924833	CTCTGGTTATGTTAC[A/G]TAATTACATGGAAAT	9873
rs3207375	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72924762	AATGGTGTCATCTAG[C/T]GGTGTAAGCACTATA	9873
rs3217361	in-del	-/GGG	0.372547	0.217904	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843362	CAAAACAAGTTTACA[-/GGG]CACACAATTTAGACA	9873
rs3223742	microsatellite	(CA)20/21/22/23/24/27	0.683178	0.165982	intron-variant	FCHSD2	GRCh38.p7	11:72959855	GGTATATTGATATNA[(CA)20/21/22/23/24/27]CCTAGAAACTTAAAA	9873
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	9873
rs3814730	snp	A/G	0.222333	0.248464	intron-variant	FCHSD2	GRCh38.p7	11:72844508	AGCAGCAATCCACCA[A/G]CATCAGCCACCCACA	9873
rs3862796	snp	C/T	0.297128	0.245518	intron-variant	FCHSD2	GRCh38.p7	11:72994477	TTAAATAATTTACTC[C/T]GAGTCACACGGCAAG	9873
rs3903492	snp	A/G	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72956524	agagaaattaatgct[A/G]ttgattataagtcaa	9873
rs4102512	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72994592	CTcacggtgaaaccc[C/T]gtctctactaaaaat	9873
rs4329714	snp	A/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72965562	AAACTCAATATTTTC[A/T]TGTATTTATTTCTGA	9873
rs4373969	snp	A/G	0.0182019	0.0936463	intron-variant	FCHSD2	GRCh38.p7	11:72914101	ctcgctgcaaactgc[A/G]cttcctgggttcaag	9873
rs4394861	snp	C/T	0.457271	0.139781	intron-variant	FCHSD2	GRCh38.p7	11:73089925	AAAAGCCTACCCTTA[C/T]CAGATGTTAAAAATT	9873
rs4400839	snp	G/T	0.361474	0.223771	intron-variant	FCHSD2	GRCh38.p7	11:72964620	CTTCTATCATCATCA[G/T]CAGCAGCAGAATCTT	9873
rs4465389	snp	A/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72954197	cagtagatgtgggga[A/T]ttttttttttttttt	9873
rs4480564	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72932177	TTATTGATTCCACTT[C/T]TTAAATATTTACCAA	9873
rs4515995	snp	A/G	0.404035	0.196909	intron-variant	FCHSD2	GRCh38.p7	11:72976750	cagaatcaaatccat[A/G]catctacagtgaact	9873
rs4578418	snp	G/T	0.143284	0.226079	intron-variant	FCHSD2	GRCh38.p7	11:72980647	CTAATTTGCAATCAT[G/T]TATATATGTATGTGT	9873
rs4594026	snp	A/G	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72964552	TTTTGTTGCCTTTTC[A/G]TCTGGAGTCTAGCAG	9873
rs4643105	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72964505	AACAGTACACATCTG[C/T]CTTCTTCATTCCTTA	9873
rs4944015	snp	A/G	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72846162	TACTCATGATGAGTA[A/G]GCTGCTCCTCCTTTT	9873

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