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
rs3712699	snp	A/G	0.5	0	intron-variant	Fancl	GRCm38.p3	11:26405627	CTGCGTGTGGTGCTC[A/G]TTGCTGTTTCTGCTT	67030
rs3719024	snp	A/G	0.5	0	intron-variant	Fancl	GRCm38.p3	11:26470846	GGATGGCATGTGTCC[A/G]CTGACATGATCTACA	67030
rs4228630	snp	G/T	0.375	0.216506	missense, nc-transcript-variant	Fancl	GRCm38.p3	11:26387223	CAGGCTTGCTTCTGC[G/T]TCGTCCATGGCGCAC	67030
rs4228631	snp	G/T	0.487535	0.077957	missense, nc-transcript-variant	Fancl	GRCm38.p3	11:26387219	CTTGCTTCTGCTTCG[G/T]CCATGGCGCACAGGA	67030
rs4228632	snp	A/T	0.21875	0.248039	utr-variant-5-prime, nc-transcript-variant	Fancl	Mm_Celera	11:26387138	TCGGCGGGAAAAACT[A/T]ACTGGTGGGTACGCT	67030
rs4228633	snp	A/G	0.21875	0.248039	utr-variant-5-prime, nc-transcript-variant	Fancl	GRCm38.p3	11:26387112	ACGCTGCCCTGACCT[A/G]GACAATGAACTGGGC	67030
rs4228634	snp	A/T	0.21875	0.248039	upstream-variant-2KB	Fancl	Mm_Celera	11:26387046	AAAGGAAGATCACTC[A/T]CAAGTCCACAGGCCT	67030
rs4228635	snp	A/C	0.21875	0.248039	upstream-variant-2KB	Fancl	GRCm38.p3	11:26386976	AAAACTAGCAAAATC[A/C]TCTTGTTGATTTCAT	67030
rs4228636	snp	C/T	0.21875	0.248039	upstream-variant-2KB	Fancl	GRCm38.p3	11:26386973	ACTAGCAAAATCCTC[C/T]TGTTGATTTCATTGA	67030
rs4228637	snp	C/G	0.314099	0.241643	upstream-variant-2KB	Fancl	GRCm38.p3	11:26386971	TAGCAAAATCCTCTT[C/G]TTGATTTCATTGAAG	67030
rs4228638	snp	C/T	0.21875	0.248039	upstream-variant-2KB	Fancl	GRCm38.p3	11:26386923	GCTGACTTTCCTACT[C/T]TGACAGGGCATTTAC	67030
rs4228639	snp	A/T	0.21875	0.248039	upstream-variant-2KB	Fancl	Mm_Celera	11:26386878	ATACTGTTTTTACCC[A/T]GAACCTGCCCCATCA	67030
rs6281835	snp	G/T	0.5	0	intron-variant	Fancl	Mm_Celera	11:26452124	TAGGAACTAGCCTCA[G/T]TATAAACAGATGTGA	67030
rs6282412	snp	A/G	0.5	0	intron-variant	Fancl	Mm_Celera	11:26452272	ATTTGTAAAGTAAAC[A/G]AGTaaataaaactgc	67030
rs6282489	snp	C/T	0.5	0	intron-variant	Fancl	Mm_Celera	11:26452303	cagttaataaatgga[C/T]caggaatatganaag	67030
rs6282507	snp	A/G	0.5	0	intron-variant	Fancl	Mm_Celera	11:26452315	ggancaggaatatga[A/G]aagacaattttcata	67030
rs6296040	snp	A/G	0.5	0	intron-variant	Fancl	GRCm38.p3	11:26452443	tccagtaagaatgtc[A/G]gtcatcaagaaacct	67030
rs6317700	snp	C/T	0.5	0	intron-variant	Fancl	GRCm38.p3	11:26454188	aagtcaccctccgcc[C/T]ggcaggactctggag	67030
rs6318136	snp	C/G	0.5	0	intron-variant	Fancl	Mm_Celera	11:26454246	tctgtacacagctca[C/G]tgccccacaAAAAGC	67030
rs6318678	snp	A/G	0.5	0	intron-variant	Fancl	Mm_Celera	11:26454343	tcttgtgtgtgccta[A/G]aatatcttgttaata	67030
rs6332056	snp	C/T	0.5	0	intron-variant	Fancl	GRCm38.p3	11:26454457	aaaagtccatagact[C/T]tcaactgtgggctcc	67030
rs6332119	snp	C/T	0.5	0	intron-variant	Fancl	GRCm38.p3	11:26454494	attgcaagcaagtta[C/T]atactttctcactcc	67030
rs6333143	snp	C/G	0.5	0	intron-variant	Fancl	GRCm38.p3	11:26454661	tccagaattgccatc[C/G]aaagcacacacagct	67030
rs6333193	snp	C/T	0.5	0	intron-variant	Fancl	Mm_Celera	11:26454700	aggctcaagacagtt[C/T]cactttatagctgtc	67030
rs6333715	snp	A/T	0.5	0	intron-variant	Fancl	GRCm38.p3	11:26454796	agtagaggctgtatc[A/T]taactattggngtct	67030
rs6333736	snp	C/T	0.5	0	intron-variant	Fancl	GRCm38.p3	11:26454807	tatcntaactattgg[C/T]gtctgtagctatact	67030
rs6334157	snp	A/C	0.5	0	intron-variant	Fancl	GRCm38.p3	11:26454827	gtagctatactgacc[A/C]tgccacatagccagc	67030
rs26827368	snp	C/T	0.124444	0.216185	intron-variant	Fancl	GRCm38.p3	11:26460958	CTTTTAGCTCTTCTT[C/T]CTGCCTCAAGCAATG	67030
rs26827369	snp	C/T	0.444444	0.157135	intron-variant	Fancl	Mm_Celera	11:26460928	CAGCCAAGTTTTAGA[C/T]ACATTCTGCATTTAC	67030
rs26827370	snp	C/T	0.48	0.0979796	intron-variant	Fancl	GRCm38.p3	11:26460895	TTTTCTATTAGTTTC[C/T]TTATTGTTCAGCTTA	67030
rs26827371	snp	A/T	0.444444	0.157135	intron-variant	Fancl	GRCm38.p3	11:26460771	ATAATTAACCAATTA[A/T]AATGTATTTGTCAAG	67030
rs26827372	snp	A/G	0.124444	0.216185	intron-variant	Fancl	Mm_Celera	11:26460486	TTCTCACTACATTAT[A/G]GTAATAGCTGCTTAT	67030
rs26827373	snp	G/T	0.391111	0.206368	intron-variant	Fancl	Mm_Celera	11:26459940	AGATGAAATTTCTTT[G/T]TGTGGATTCAACTAT	67030
rs26827374	snp	C/T	0.46875	0.121031	intron-variant	Fancl	Mm_Celera	11:26459501	TCCTGATAATGCAGA[C/T]GAGTGACAATGACTG	67030
rs26827375	snp	C/T	0.165289	0.235211	intron-variant	Fancl	GRCm38.p3	11:26452949	TGTAAATCTAGTATC[C/T]GGTCTGTTGCTCGTG	67030
rs26827376	snp	C/G	0.444444	0.157135	intron-variant	Fancl	GRCm38.p3	11:26436223	AGCAAACAGGATTAA[C/G]TAGTAGTAACTGGAA	67030
rs26827377	snp	A/G	0.18	0.24	intron-variant	Fancl	GRCm38.p3	11:26435506	TTTAGGCTTGTGAGA[A/G]TTCAGATAATTAACC	67030
rs26827378	snp	A/G	0.5	0	intron-variant	Fancl	GRCm38.p3	11:26435333	GTGTTGTTGTGTGTA[A/G]GCACTGGGTTGTTGT	67030
rs26827379	snp	A/G	0.5	0	intron-variant	Fancl	GRCm38.p3	11:26435109	CACTAGGTCAGGGTT[A/G]ACAGTTGACAGTACC	67030
rs26827380	snp	A/G	0.277778	0.248452	intron-variant	Fancl	GRCm38.p3	11:26434995	AGAAACTGGTGTTAT[A/G]TACAAAGAAGGTGAT	67030
rs26827381	snp	G/T	0.21875	0.248039	intron-variant	Fancl	GRCm38.p3	11:26434742	ATTGTCTAGATATCT[G/T]TAGGCAAGCATGTAG	67030
rs26827382	snp	G/T	0.345679	0.230967	intron-variant	Fancl	GRCm38.p3	11:26434080	CCTCAGTTCATAGCA[G/T]GAGCACCGATACTGA	67030
rs26827383	snp	C/G	0.375	0.216506	intron-variant	Fancl	GRCm38.p3	11:26433396	AAAAAAATGTTAAAG[C/G]TATGTTTCCTCTTCC	67030
rs26827384	snp	A/G	0.124444	0.216185	intron-variant	Fancl	GRCm38.p3	11:26425918	AACCAAGACTGGCCA[A/G]TTGAAGATCCTCAGG	67030
rs26827385	snp	C/T	0.391111	0.206368	intron-variant	Fancl	GRCm38.p3	11:26425041	AAGGCCATCTATACT[C/T]AGAGCCATCAAAACA	67030
rs26827386	snp	C/T	0.444444	0.157135	intron-variant	Fancl	GRCm38.p3	11:26424729	TTAGTGCCTGGCTTT[C/T]TTCAAGAGAGATTTA	67030
rs26827387	snp	A/T	0.375	0.216506	intron-variant	Fancl	GRCm38.p3	11:26424533	CTGTGTGATGAGCAC[A/T]GCTCCCAGGGTGTGT	67030
rs26827388	snp	C/T	0.124444	0.216185	intron-variant	Fancl	GRCm38.p3	11:26424415	GAATACAGTACTGAT[C/T]TGAGCTACACAACTC	67030
rs26827389	snp	A/T	0.444444	0.157135	intron-variant	Fancl	GRCm38.p3	11:26423626	GGGCAGAGTGTGAGA[A/T]TTTGAGTGCCTCTGT	67030
rs26827390	snp	A/G	0.21875	0.248039	intron-variant	Fancl	GRCm38.p3	11:26423545	AACAAGGGTCTTTCT[A/G]TGTCTTCATTCAGGT	67030
rs26827391	snp	A/T	0.48	0.0979796	intron-variant	Fancl	GRCm38.p3	11:26423354	ATGCCCACATGGGAC[A/T]TTTAGGTGTAATATC	67030
rs26827392	snp	C/T	0.408163	0.193609	intron-variant	Fancl	GRCm38.p3	11:26423320	GCCAGGAGACGGCTT[C/T]AGTAGTGACTCTTTT	67030
rs26827393	snp	C/G	0.444444	0.157135	intron-variant	Fancl	GRCm38.p3	11:26423314	AGTGATGCCAGGAGA[C/G]GGCTTTAGTAGTGAC	67030
rs26827394	snp	A/G	0.391111	0.206368	intron-variant	Fancl	GRCm38.p3	11:26423150	TTTGGGGAGTCATCA[A/G]TCACTTGTATTTCAG	67030
rs26827395	snp	G/T	0.444444	0.157135	intron-variant	Fancl	GRCm38.p3	11:26423107	CACTGAAATGTAAAG[G/T]ACGCCAGGACATCCA	67030
rs26827396	snp	A/G	0.132653	0.220748	intron-variant	Fancl	GRCm38.p3	11:26422779	ACCATTGTTCTGGGA[A/G]CATCTTTTGCATCTT	67030
rs26827397	snp	A/T	0.124444	0.216185	intron-variant	Fancl	GRCm38.p3	11:26422755	AATAGCTCCAGACAC[A/T]ATGATGTTACCATTG	67030
rs26827398	snp	C/T	0.497778	0.0332592	intron-variant	Fancl	GRCm38.p3	11:26422566	TTTGAATATTTTCAC[C/T]GTTTAGAAGTGCTCG	67030
rs26827399	snp	C/G	0.391111	0.206368	intron-variant	Fancl	GRCm38.p3	11:26421956	ATAGGATTAATTTGA[C/G]TGTGTGAACTAACAC	67030
rs26827400	snp	A/G	0.132653	0.220748	intron-variant	Fancl	GRCm38.p3	11:26421886	TATATTTTGTGCAAA[A/G]GAGAAATTTATTGCT	67030
rs26827401	snp	C/T	0.497778	0.0332592	intron-variant	Fancl	GRCm38.p3	11:26421564	CCTTGAGTTCTTCAT[C/T]CATCTGGGTGATGAG	67030
rs26827402	snp	A/G	0.444444	0.157135	intron-variant	Fancl	GRCm38.p3	11:26420977	AAACTGGAGTTTTAT[A/G]CTTTAGAAATCCCTC	67030
rs26827403	snp	C/T	0.46281	0.131194	intron-variant	Fancl	GRCm38.p3	11:26420884	CCACTTTCCTCTGTT[C/T]CAGCCGGTGCACTTA	67030
rs26827404	snp	A/G	0.391111	0.206368	intron-variant	Fancl	GRCm38.p3	11:26420792	TCTCCTGTGTTAAAA[A/G]GAAATGCCCATATTT	67030
rs26827405	snp	A/T	0.336735	0.234472	intron-variant	Fancl	GRCm38.p3	11:26420509	GCTCTTGATTCTCAC[A/T]TTAGTAGTTACAGAT	67030
rs26827406	snp	C/T	0.260355	0.249785	intron-variant	Fancl	GRCm38.p3	11:26420440	CAAGAGATACACACA[C/T]ATTAGGTCTAGTTTG	67030
rs26827407	snp	C/T	0.391111	0.206368	intron-variant	Fancl	GRCm38.p3	11:26420319	TACATACCTCCATCG[C/T]CTCTCTCTGTGCTGT	67030
rs26827408	snp	A/G	0.165289	0.235211	intron-variant	Fancl	GRCm38.p3	11:26420279	TGCTCAACCATAAGA[A/G]TGGAATGTCAAAGGT	67030
rs26827409	snp	A/G	0.408163	0.193609	intron-variant	Fancl	GRCm38.p3	11:26420273	AGTTGATGCTCAACC[A/G]TAAGAGTGGAATGTC	67030
rs26827410	snp	A/C	0.408163	0.193609	intron-variant	Fancl	GRCm38.p3	11:26420044	TTACATGAAAGGACA[A/C]CGCTTTGAGGCTAGA	67030
rs26827411	snp	A/G	0.444444	0.157135	intron-variant	Fancl	GRCm38.p3	11:26419993	CACTTGTGCTGAGTT[A/G]ATGAAAGAAAAGAAA	67030
rs26827412	snp	C/T	0.244898	0.249948	intron-variant	Fancl	GRCm38.p3	11:26417241	TGCTGTGTGAATGGA[C/T]TGTGAGAAGCATGGA	67030
rs26827413	snp	A/G	0.197531	0.244432	intron-variant	Fancl	GRCm38.p3	11:26416451	GCACCTTAAACTACC[A/G]CATGGAACTTACCAT	67030
rs26827414	snp	G/T	0.46875	0.121031	intron-variant	Fancl	GRCm38.p3	11:26416319	TTGAGGCGAATCCTA[G/T]AATGAAATTGATTGA	67030
rs26827415	snp	C/T	0.21875	0.248039	intron-variant	Fancl	GRCm38.p3	11:26413945	CCAGGTTGGAAAGTG[C/T]GATTAAACAGGTTAG	67030
rs26827416	snp	A/G	0.46875	0.121031	intron-variant	Fancl	GRCm38.p3	11:26413911	GTAGGCTGCAGCACT[A/G]TGTCCAGTAGTCTTT	67030
rs26827417	snp	A/G	0.408163	0.193609	intron-variant	Fancl	GRCm38.p3	11:26413380	TACAAAAGGTACAAA[A/G]GAATGCAATGCTGTT	67030
rs26827418	snp	A/G	0.5	0	intron-variant	Fancl	GRCm38.p3	11:26411396	AAGTGCAGCTGCCCT[A/G]TGAGATGCAGGAAGT	67030
rs26827419	snp	A/G	0.18	0.24	intron-variant	Fancl	GRCm38.p3	11:26411164	GCTAATAGCAACGGC[A/G]TGTAGATGTGTACTT	67030
rs26827420	snp	C/T	0.46875	0.121031	intron-variant	Fancl	GRCm38.p3	11:26410766	GGGTGCAGCTTCTCA[C/T]TGTGCTCCTTAGAAA	67030
rs26827421	snp	A/G	0.473373	0.11227	intron-variant	Fancl	GRCm38.p3	11:26396349	GCTGTTTTCGTGTCC[A/G]TGGTGAATTTCCTAC	67030
rs26827422	snp	C/T	0.5	0	intron-variant	Fancl	GRCm38.p3	11:26395409	TTTGTGTCATAGCTC[C/T]GCGGACTGGGGCCAC	67030
rs26827423	snp	C/T	0.297521	0.245442	intron-variant	Fancl	GRCm38.p3	11:26395363	CTGTTCTCCTTGGCT[C/T]CATCATTACCTTTGC	67030
rs26827424	snp	A/G	0.42	0.183303	intron-variant	Fancl	GRCm38.p3	11:26392930	CCTCCTTCCAATACA[A/G]TACTGCTTTGCATAA	67030
rs26827425	snp	A/T	0.46281	0.131194	intron-variant	Fancl	GRCm38.p3	11:26392871	TAGTTCTGTGGTTGC[A/T]TGTTTTCCACTGTGT	67030
rs26827426	snp	G/T	0.473373	0.11227	intron-variant	Fancl	GRCm38.p3	11:26392810	GGTTGGACTACACCA[G/T]GATTGAGTGAGCTGG	67030
rs26827427	snp	A/T	0.396694	0.202437	intron-variant	Fancl	GRCm38.p3	11:26392790	CAAGGAGTTCTACTT[A/T]GGCTGGTTGGACTAC	67030
rs26827428	snp	A/G	0.375	0.216506	intron-variant	Fancl	GRCm38.p3	11:26392735	AATTTAGCTGTACCC[A/G]TGAAACTACTTTTCT	67030
rs26827429	snp	A/G	0.197531	0.244432	intron-variant	Fancl	Mm_Celera	11:26389819	CTTTAAGAGGATCTG[A/G]TAGATGCTTCGGTAT	67030
rs26827430	snp	C/T	0.46281	0.131194	intron-variant	Fancl	GRCm38.p3	11:26389691	TGTTATACGGAACAG[C/T]TTTCCCATCTTACTT	67030
rs26827431	snp	A/T	0.42	0.183303	intron-variant	Fancl	Mm_Celera	11:26388964	GTTCTTTGGGCCATT[A/T]CACATTCACTTATAT	67030
rs26827432	snp	A/G	0.473373	0.11227	intron-variant	Fancl	Mm_Celera	11:26388457	TCTTAAGCACTGTCT[A/G]AAAGCTATCCAGCAC	67030
rs26827433	snp	A/G	0.473373	0.11227	intron-variant	Fancl	Mm_Celera	11:26388386	TTAGACCGGAAATAC[A/G]TTAGCCTTCGATGTA	67030
rs26827434	snp	C/T	0.46281	0.131194	intron-variant	Fancl	Mm_Celera	11:26388103	ATGAGTTAGCCACCT[C/T]TTGCTTAACTGTTGA	67030
rs26827435	snp	A/G	0.5	0	intron-variant	Fancl	Mm_Celera	11:26387936	GCTGAGCAGATACCA[A/G]ATTTTCTAAATAGTA	67030
rs26827436	snp	C/T	0.132653	0.220748	intron-variant	Fancl	Mm_Celera	11:26387911	GTGTTGAAGCAACAA[C/T]CTCTAGAATGCTGAG	67030
rs26827437	snp	A/T	0.489796	0.070696	intron-variant	Fancl	GRCm38.p3	11:26387582	TTACTACACTTACGA[A/T]TTTGATTTATAGAGC	67030
rs26827438	snp	A/G	0.142012	0.225474	intron-variant	Fancl	Mm_Celera	11:26387358	CCTGTCACTCGTGGC[A/G]AAGCCTGACCGCGGC	67030
rs26827439	snp	A/G	0.244898	0.249948	synonymous-codon, nc-transcript-variant	Fancl	Mm_Celera	11:26387259	CCATTTCCCGCTGCT[A/G]CTTCCTCAGAACCGG	67030
rs26827440	snp	A/G	0.426035	0.177515	upstream-variant-2KB	Fancl	GRCm38.p3	11:26386847	TAGTCCAGAGCAAAC[A/G]CAAGAACAGGAGAGG	67030

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