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
rs3727	snp	C/T	0.0279526	0.114869	utr-variant-3-prime	FEM1C	GRCh38.p7	5:115521013	ATACAGTACTTCTTT[C/T]GAAAAAATACACAAT	56929
rs166281	snp	A/C	0.0228947	0.104514	intron-variant	FEM1C	GRCh38.p7	5:115529745	GAAAGAGATCTTAGA[A/C]CACGTTAACACCAAT	56929
rs256938	snp	A/C	0.460589	0.13473	intron-variant	FEM1C	GRCh38.p7	5:115532640	TTATAATCAGTATAT[A/C]TATAACTGTTTCCTG	56929
rs256939	snp	C/T	0.48435	0.0870631	intron-variant	FEM1C	GRCh38.p7	5:115532541	ATGCCTTTTTTTTTT[C/T]CCCTCTGTTTTCTAA	56929
rs256940	snp	A/G	0.383053	0.211653	intron-variant	FEM1C	GRCh38.p7	5:115530494	aaaaccagtaaggat[A/G]aagatttgaacatta	56929
rs256956	snp	G/T	0.491936	0.0629843	intron-variant	FEM1C	GRCh38.p7	5:115541325	TTTTCCAGAGGAAGT[G/T]TAAAAATCCCACAAA	56929
rs256957	snp	A/G	0.0260105	0.111035	intron-variant	FEM1C	GRCh38.p7	5:115542223	AAATTATACACAATC[A/G]AAAACCGGAGCCCTT	56929
rs256958	snp	A/G	0.21695	0.247806	intron-variant	FEM1C	GRCh38.p7	5:115542368	TGCTATATTTAATGC[A/G]TGTTCTTATAAAAGG	56929
rs256959	snp	C/T	0.495016	0.0496707	upstream-variant-2KB	FEM1C	GRCh38.p7	5:115545833	ATTTGATGCTAAAAC[C/T]TACGTTGCATTAAAC	56929
rs372702	snp	A/G	0.45946	0.136478	intron-variant	FEM1C	GRCh38.p7	5:115526911	CCTTCTGGGAGTCTA[A/G]AATTTTGGGTATGAG	56929
rs813761	snp	A/G	0.486855	0.0799975	intron-variant	FEM1C	GRCh38.p7	5:115536030	aacttaagacagaaa[A/G]gagattactggttgc	56929
rs2161346	snp	A/G	0.000798403	0.0199641	intron-variant	FEM1C	GRCh38.p7	5:115538561	TATGTAGTAGAATGC[A/G]GTTAGATGTCACAGT	56929
rs3776801	snp	A/G	0.173965	0.238157	utr-variant-3-prime	FEM1C	GRCh38.p7	5:115523956	TGTGAATTTTATACA[A/G]TTGAAAGTCTTTTTT	56929
rs3776802	snp	C/G	0.172028	0.23753	utr-variant-3-prime	FEM1C	GRCh38.p7	5:115523909	AAAGTAGAAACAGGG[C/G]GGAAACTTGAGAAGA	56929
rs3984997	snp	C/G			utr-variant-3-prime	FEM1C	GRCh38.p7	5:115523129	AAGTTATCTTTAAAG[C/G]TATACATAAGCTTGA	56929
rs3984998	snp	A/G			utr-variant-3-prime	FEM1C	GRCh38.p7	5:115523133	TATCTTTAAAGGTAT[A/G]CATAAGCTTGAAGAA	56929
rs5870659	in-del	-/A	0	0	intron-variant	FEM1C	GRCh38.p7	5:115529253	GACATACAACACAGC[-/A]AAACTGCTGAAAACT	56929
rs5870660	in-del	-/A/AA	0.431916	0.171483	intron-variant	FEM1C	GRCh38.p7	5:115535284	TAAAAAAAAAAAAAA[-/A/AA]CAAACACAGAATGAG	56929
rs6868540	snp	C/G	0.0471551	0.14613	upstream-variant-2KB	FEM1C	GRCh38.p7	5:115545076	CCTCTCGGATTTTCG[C/G]GGTGCTCCCTTAGGG	56929
rs6871805	snp	A/G			intron-variant	FEM1C	GRCh38.p7	5:115528077	TCGAAAAAATACAAA[A/G]TATATTTATTTTGAA	56929
rs6878790	snp	C/T	0.482831	0.0910472	upstream-variant-2KB	FEM1C	GRCh38.p7	5:115546504	GACCTGTCTCTCTCA[C/T]CTAATTCAATAAGAT	56929
rs6893854	snp	A/T	0.457737	0.139088	intron-variant	FEM1C	GRCh38.p7	5:115530224	atgccctttgcaaaa[A/T]ctaaatattaagaag	56929
rs6894123	snp	A/G	0.457271	0.139781	intron-variant	FEM1C	GRCh38.p7	5:115530179	atatgggtagaaaat[A/G]atctttagaagtgaa	56929
rs7712026	snp	A/G	0.18134	0.240387	downstream-variant-500B	FEM1C	GRCh38.p7	5:115520610	AATAATATATTTATG[A/G]TATACTTCTGATCAC	56929
rs7730778	snp	A/C/G	0.0170251	0.090679	intron-variant	FEM1C	GRCh38.p7	5:115542197	TGCTTTTAGTTTATT[A/C/G]CAATCAACAAAAATT	56929
rs7736971	snp	A/T	0.00874735	0.0655527	intron-variant	FEM1C	GRCh38.p7	5:115528564	AGATCATCTCATTAT[A/T]GATTTGAAATAATCC	56929
rs10043328	snp	A/C			intron-variant	FEM1C	GRCh38.p7	5:115543820	CCACACACCCCCCCC[A/C]CCCCCAAAGAAAAGG	56929
rs10053572	snp	C/G	0.452965	0.145963	intron-variant	FEM1C	GRCh38.p7	5:115541847	GCATGCTTGTACATA[C/G]ACAAGTATGCTTGTA	56929
rs10077232	snp	A/T			intron-variant	FEM1C	GRCh38.p7	5:115530041	tttaatttaaacatt[A/T]aaaagacagaaactg	56929
rs11330098	in-del	-/A			utr-variant-3-prime	FEM1C	GRCh38.p7	5:115521092	GCAAAAAAAAAAAAA[-/A]GAAAAAGAAAAAAAG	56929
rs11960440	snp	G/T	0.00517822	0.0506191	intron-variant	FEM1C	GRCh38.p7	5:115530616	aaatactgaccatat[G/T]cttggccgtaaggca	56929
rs12110084	snp	C/G/T	0.0187777	0.0950591	intron-variant	FEM1C	GRCh38.p7	5:115527351	TATTGAATCTTTCCA[C/G/T]AAGTTTATCCTGTTT	56929
rs12110088	snp	A/C	0.0134861	0.0810011	intron-variant	FEM1C	GRCh38.p7	5:115527515	CTGACTATCGATGTT[A/C]ATTTGTTTAAAATAA	56929
rs12187973	snp	G/T	0.480853	0.0959518	utr-variant-3-prime	FEM1C	GRCh38.p7	5:115522740	TCACAGGTAAACTGA[G/T]TTTTTCTCAAATCAA	56929
rs13162494	snp	A/G	0.0693013	0.172766	intron-variant, missense	FEM1C	GRCh38.p7	5:115529571	aggaagatgaGCCAC[A/G]TGGAAGCCTGGAGAT	56929
rs13177180	snp	A/G	0.455621	0.142197	upstream-variant-2KB, utr-variant-5-prime	FEM1C	GRCh38.p7	5:115544896	TAggcgcggggcggg[A/G]cgtcgcggccggggt	56929
rs13356084	snp	C/G	0.469247	0.120128	intron-variant, upstream-variant-2KB	FEM1C	GRCh38.p7	5:115544270	TCACCCCCCACCCCC[C/G]GCCAAGGGATGATCC	56929
rs13357862	snp	C/T	0.454061	0.144427	upstream-variant-2KB	FEM1C	GRCh38.p7	5:115546756	ACACATGCACGCACA[C/T]GCACACACACACAAA	56929
rs17137954	snp	C/T	0.0603597	0.1629	intron-variant	FEM1C	GRCh38.p7	5:115527583	AAACACTCTTTTGTA[C/T]TAAGGACCTCTACTA	56929
rs17137960	snp	A/C	0.0138799	0.0821421	intron-variant	FEM1C	GRCh38.p7	5:115537456	GAGGATTCACAGTTC[A/C]AAATCCAATCTCCAG	56929
rs17137963	snp	G/T	0.0138799	0.0821421	intron-variant	FEM1C	GRCh38.p7	5:115540133	GGAAAAATCCTCTCT[G/T]GCTGCTAAATCACAT	56929
rs17472710	snp	A/T	0.102726	0.202016	intron-variant	FEM1C	GRCh38.p7	5:115532223	TAATGCTACTGCTTC[A/T]CAAATAAGTTCTTAC	56929
rs17852534	snp	A/G/T	0.000115638	0.00760302	synonymous-codon	FEM1C	GRCh38.p7	5:115525025	TAATAAGCTGCTGGC[A/G/T]GTCATTGGGCTTAAA	56929
rs33910606	in-del	-/C	0.499515	0.0155675	intron-variant	FEM1C	GRCh38.p7	5:115543812	ACTCCATCCCACACA[-/C]CCCCCCCACCCCCAA	56929
rs34179881	snp	C/T			utr-variant-3-prime	FEM1C	GRCh38.p7	5:115521332	CTTTTCCCATATAAC[C/T]TAAACAATTTTCCCA	56929
rs34470526	in-del	-/A			intron-variant	FEM1C	GRCh38.p7	5:115534343	ATGTTCAACTGTGAA[-/A]GCTTAGGTGCCTAGG	56929
rs34984849	in-del	-/T			utr-variant-3-prime	FEM1C	GRCh38.p7	5:115522872	TACCTGAATCTTTTT[-/T]AGTACTTTTCACTTA	56929
rs35045234	in-del	-/G			intron-variant	FEM1C	GRCh38.p7	5:115533031	GTATGAATTTTATTG[-/G]CATGTAAATAAGTCA	56929
rs36043124	in-del	-/A			intron-variant	FEM1C	GRCh38.p7	5:115540498	ATACTGATACTGGGG[-/A]AAAAAATGACTTAGA	56929
rs55797760	snp	C/T	0.297382	0.245469	intron-variant	FEM1C	GRCh38.p7	5:115542283	TAGCCAACAAATCCA[C/T]ATCTGTTTAATCTAG	56929
rs55820160	snp	A/C	0.173643	0.238054	intron-variant	FEM1C	GRCh38.p7	5:115539429	GCTCTGAGAAGGACT[A/C]ACCTAATCACTACAG	56929
rs55825428	snp	C/T	0.336245	0.234652	intron-variant, upstream-variant-2KB	FEM1C	GRCh38.p7	5:115544366	GCCCCCTCCCAATCT[C/T]CTCCATCGACCACAA	56929
rs56001355	snp	C/T			intron-variant	FEM1C	GRCh38.p7	5:115531217	ATGAATAAATTATAT[C/T]TAATATAAAACCAAA	56929
rs56087439	in-del	-/A	0.488057	0.0763479	intron-variant	FEM1C	GRCh38.p7	5:115542564	CTCCAAGGTTGTTCT[-/A]AAAAAAAAAAAAACA	56929
rs56110877	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	FEM1C	GRCh38.p7	5:115544916	GCGGCCGGGGTGGGG[C/T]GACGGGGAGGGGGCG	56929
rs56212105	snp	A/G	0.237303	0.249677	intron-variant	FEM1C	GRCh38.p7	5:115530624	ACCATATTCTTGGCC[A/G]TAAGGCAAGTCTCAA	56929
rs57829926	snp	C/T	0.0158469	0.0875917	upstream-variant-2KB	FEM1C	GRCh38.p7	5:115545221	GCACTCAGAGTTCCA[C/T]GTGGCTGGGGAGGCC	56929
rs57948082	snp	A/G	0.0150606	0.0854603	intron-variant	FEM1C	GRCh38.p7	5:115538629	ACAAACAAGCAAACA[A/G]ACAAACCACTCCAGT	56929
rs58132177	snp	C/T			intron-variant	FEM1C	GRCh38.p7	5:115534860	GTGATACCTACGCTG[C/T]TGGTCCTTGAGTAGC	56929
rs58762176	snp	A/G	0.00478085	0.0486577	intron-variant	FEM1C	GRCh38.p7	5:115527685	TTTTCTCTATTCAGA[A/G]TAGCACAAAATCAAG	56929
rs58897289	in-del	-/A			intron-variant	FEM1C	GRCh38.p7	5:115528002	AAAAAAAAAAAAAAA[-/A]GGTAGCAAAAGCCAA	56929
rs60413296	snp	C/T			intron-variant	FEM1C	GRCh38.p7	5:115539778	TGCTCTTTGTATATC[C/T]TAAGTCTAACAGCCT	56929
rs60640600	snp	A/C	0.173643	0.238054	intron-variant	FEM1C	GRCh38.p7	5:115539430	CTCTGAGAAGGACTC[A/C]CCTAATCACTACAGA	56929
rs62371181	snp	C/T	0.5	0	intron-variant	FEM1C	GRCh38.p7	5:115533275	CTTTATTTTCTTTTA[C/T]GCCATGTCTATGTTT	56929
rs72817107	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FEM1C	GRCh38.p7	5:115524118	TTCACAAACAATATA[C/T]TATATGGTATATTTA	56929
rs72817110	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1C	GRCh38.p7	5:115537354	TGAAACGTAACTTCT[A/G]TCTTAAGCTCATGTT	56929
rs72817112	snp	C/G	0.0471551	0.14613	upstream-variant-2KB	FEM1C	GRCh38.p7	5:115545602	GAAATTTCAGAAAAT[C/G]TGATTAGTTTTGGAG	56929
rs72817114	snp	A/G	0.0123036	0.0774623	upstream-variant-2KB	FEM1C	GRCh38.p7	5:115545823	AACCTCTGGAATTTG[A/G]TGCTAAAACCTACGT	56929
rs73251202	snp	A/C	0.0174175	0.0916809	utr-variant-3-prime	FEM1C	GRCh38.p7	5:115522472	ATTTACCTTTTCTTA[A/C]TGGTGAAATCAAATT	56929
rs73253004	snp	A/C	0.0170251	0.090679	utr-variant-3-prime	FEM1C	GRCh38.p7	5:115523802	TAAAGCACTTATGGT[A/C]ACTGCAAATGGTAAC	56929
rs73253005	snp	A/G	0.15207	0.230021	synonymous-codon	FEM1C	GRCh38.p7	5:115524464	CTTCTCATCCAGCAA[A/G]TCACTAGCAGTTTGT	56929
rs73253008	snp	C/G	0.0205511	0.0992634	intron-variant	FEM1C	GRCh38.p7	5:115535602	GAAGAAGAAGAAGAA[C/G]AAGTGTTGGAGAGGG	56929
rs73253009	snp	A/T	0.0166325	0.0896639	intron-variant	FEM1C	GRCh38.p7	5:115535645	GGAACTCTTCTTACA[A/T]TGCTGACAGGAATGT	56929
rs73253014	snp	A/C	0.127944	0.218179	upstream-variant-2KB	FEM1C	GRCh38.p7	5:115546768	ACACGCACACACACA[A/C]AAAAAATTAGTCAGG	56929
rs73780315	snp	A/G	0.124144	0.21601	intron-variant	FEM1C	GRCh38.p7	5:115535051	TCCTCTTTACTCTAA[A/G]TTTAACCATATGCCA	56929
rs73780316	snp	A/G	0.0648419	0.167978	intron-variant	FEM1C	GRCh38.p7	5:115537981	TGGGGAATTAAATAA[A/G]ATTTTTCTTTAGCAT	56929
rs73780317	snp	A/C	0.00478085	0.0486577	intron-variant	FEM1C	GRCh38.p7	5:115540004	ATGTACTGACATTTT[A/C]TTTCCTCAGAACCAT	56929
rs74327648	snp	G/T	0.021333	0.101051	utr-variant-3-prime	FEM1C	GRCh38.p7	5:115524216	TGATATCAATCAAGC[G/T]AAATGAATGCTGGTG	56929
rs74395157	snp	C/G	0.00199481	0.0315187	intron-variant	FEM1C	GRCh38.p7	5:115530795	AAGCCCAATGAAAAT[C/G]AGAAAATTTTTTTAA	56929
rs74621288	snp	A/C	0.120326	0.21374	intron-variant	FEM1C	GRCh38.p7	5:115540778	CTCCAATAACATAGG[A/C]TTTTAAAACATATCC	56929
rs74713184	in-del	-/AA			intron-variant	FEM1C	GRCh38.p7	5:115542576	TCTAAAAAAAAAAAA[-/AA]CAAAACAAAAAGCTA	56929
rs74858537	snp	C/T	0.0310518	0.120672	utr-variant-3-prime	FEM1C	GRCh38.p7	5:115523530	GATCTGTTTCCCAAA[C/T]TTAGCACACAATAAT	56929
rs74863613	snp	C/T	0.0263992	0.111815	intron-variant	FEM1C	GRCh38.p7	5:115538273	GCTAGCAATCCTTGC[C/T]ACATGCCTACATGAA	56929
rs74911277	in-del	-/AA			intron-variant	FEM1C	GRCh38.p7	5:115531536	ATGATTCACTGTGCA[-/AA]TCTAACTCAGGGACT	56929
rs75167304	snp	C/T	0.0494327	0.149241	downstream-variant-500B	FEM1C	GRCh38.p7	5:115520628	TACTTCTGATCACAG[C/T]AAACCAATTAAAAAA	56929
rs75209410	snp	C/T	0.0154538	0.0865337	intron-variant	FEM1C	GRCh38.p7	5:115536372	CAGTCCTCATCTCTC[C/T]TTCTTCAGCCTACTA	56929
rs75422580	snp	A/G	0.02016	0.0983543	upstream-variant-2KB	FEM1C	GRCh38.p7	5:115545711	TGTAAAGTCAATGAG[A/G]TCAGGTTCTTGAGCT	56929
rs75479409	snp	C/G	0.0126979	0.078662	intron-variant	FEM1C	GRCh38.p7	5:115526169	CCTGGCCAGACTGCT[C/G]TTTAATATATCTAAG	56929
rs75650190	snp	C/G	0.000399281	0.0141238	intron-variant	FEM1C	GRCh38.p7	5:115538862	CCACAGATCCACATC[C/G]CAATAAACTTTCTGC	56929
rs75667088	snp	A/T	0.00119737	0.0244387	utr-variant-3-prime	FEM1C	GRCh38.p7	5:115523554	CAATAATTTCAGTGG[A/T]TTAGAGAAAGAAACC	56929
rs75771482	snp	A/G	0.5	0	utr-variant-5-prime, upstream-variant-2KB	FEM1C	GRCh38.p7	5:115544709	CACGCCCCGCCACCC[A/G]AGCTGCCTCCCGCCC	56929
rs75900621	snp	C/T	0.103082	0.202275	downstream-variant-500B	FEM1C	GRCh38.p7	5:115520778	ACATAGAAGTATTAA[C/T]AATAAATGCTATCTT	56929
rs76214589	snp	C/T	0	0	intron-variant	FEM1C	GRCh38.p7	5:115526039	TGGTCTTTTTTTTTT[C/T]CTTTAGAGACCAGGT	56929
rs76237597	snp	C/T	0.109814	0.206997	intron-variant	FEM1C	GRCh38.p7	5:115537501	ATGGATATTTCCCTA[C/T]TGGACTCAATTTGCA	56929
rs76370883	snp	C/T	0.0170251	0.090679	intron-variant	FEM1C	GRCh38.p7	5:115526639	TGCCGACCTCTGGTA[C/T]TTACATACAATGTTT	56929
rs76559752	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FEM1C	GRCh38.p7	5:115522633	TACCTAATGTGACTG[C/T]TTGCATTGATGACTC	56929
rs76722274	snp	C/T	0.00953873	0.0683987	intron-variant	FEM1C	GRCh38.p7	5:115537155	TTCATCTGGGTCTCT[C/T]CCTATCTCTTCCACT	56929
rs76767872	snp	A/G	0.5	0	intron-variant	FEM1C	GRCh38.p7	5:115528001	TGAGACTTCGTCTCA[A/G]AAAAAAAAAAAAAAA	56929
rs76942975	snp	A/T	0.0138799	0.0821421	intron-variant	FEM1C	GRCh38.p7	5:115536617	GCACTAGAAGAAGGA[A/T]TCTCTGCTTAGAATG	56929
rs76956480	snp	C/T			upstream-variant-2KB	FEM1C	GRCh38.p7	5:115546856	GGCTATAGTGAGCCA[C/T]GATCACACCACTGTG	56929

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