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
rs3023445	snp	C/T			utr-variant-3-prime	Ccnf	GRCm38.p3	17:24223673	TACCCTTCTGTGTCC[C/T]GTTGTCTCCGGGAGC	12449
rs3023446	snp	C/T	0.3848	0.210544	utr-variant-3-prime	Ccnf	GRCm38.p3	17:24223671	CCCTTCTGTGTCCTG[C/T]TGTCTCCGGGAGCAT	12449
rs3678863	snp	A/G	0.408163	0.193609	intron-variant	Ccnf	Mm_Celera	17:24244179	ACGACTACAGCAGGG[A/G]CATGAGTCATTCTGT	12449
rs3679391	snp	A/G	0.408163	0.193609	intron-variant	Ccnf	Mm_Celera	17:24244214	AATATATCAGAACTG[A/G]AATTACTCAGTTTTC	12449
rs3679485	snp	A/G	0.408163	0.193609	intron-variant	Ccnf	Mm_Celera	17:24244271	GGCTTCCATGAGAAG[A/G]TGACTCACATCTGAG	12449
rs3691006	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Ccnf, Mir6965	GRCm38.p3	17:24240987	ACAGTGCTGACTGAT[C/T]ACGGCAGAAATGAGG	12449
rs3692227	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Ccnf, Mir6965	Mm_Celera	17:24241187	CAGATCACAGAGCCC[A/G]AGACAAACCTCAAGG	12449
rs3692229	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Ccnf, Mir6965	GRCm38.p3	17:24241189	GATCACAGAGCCCGA[A/G]ACAAACCTCAAGGGA	12449
rs3692817	snp	G/T	0.5	0	intron-variant, upstream-variant-2KB	Ccnf, Mir6965	Mm_Celera	17:24241267	CACCTCCATCACTTA[G/T]CCTCCAAGCTGTCCT	12449
rs4139614	snp	C/T	0.5	0	intron-variant	Ccnf	Mm_Celera	17:24244398	TGAGCTCTCCAGTTT[C/T]CGGTCTCTTTCAGGG	12449
rs4139618	snp	C/G	0.5	0	intron-variant	Ccnf	Mm_Celera	17:24244399	GAGCTCTCCAGTTTC[C/G]GGTCTCTTTCAGGGG	12449
rs6243977	snp	A/T	0.5	0	intron-variant	Ccnf	Mm_Celera	17:24238271	GACTCAAAAACAGCA[A/T]AAAGATTAAATAGAA	12449
rs13459672	snp	C/T			utr-variant-3-prime	Ccnf	GRCm38.p3	17:24223354	TTGTATCCATGTGAC[C/T]GTATCTCTGCACTGA	12449
rs13459673	snp	C/T	0.375	0.216506	missense	Ccnf	GRCm38.p3	17:24223914	ACAGTGACAAGGACA[C/T]GCACCTGGCTTCCTG	12449
rs13459674	snp	A/G	0.375	0.216506	missense	Ccnf	GRCm38.p3	17:24226575	GCTGACTTGTGCAGT[A/G]CAATAGGAGTAAAAC	12449
rs13459675	snp	C/T			synonymous-codon	Ccnf	GRCm38.p3	17:24223985	GTGTCGTCCCCCAAA[C/T]TCCCCAGAGAGCGGT	12449
rs13459676	snp	C/T			synonymous-codon	Ccnf	GRCm38.p3	17:24224995	AATCAGGAGGAGACA[C/T]TGCTAGGCAGCCTTC	12449
rs13459677	snp	C/T			synonymous-codon	Ccnf	GRCm38.p3	17:24244533	CAGTGTGTGGGCATC[C/T]GCCAGCTTCCAGGAG	12449
rs13459678	snp	C/G	0.444444	0.157135	synonymous-codon	Ccnf	Mm_Celera	17:24224081	CATGGGGGGCTCTCC[C/G]CAATCTACCTCAGTG	12449
rs13459679	snp	A/G			synonymous-codon	Ccnf	GRCm38.p3	17:24225068	TTGCAGGAAGCGAGA[A/G]AACAGCCTTCAGGAG	12449
rs29497480	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Ccnf, Mir5134	GRCm38.p3	17:24235580	CATAGGTCCTGGGAA[C/T]TGAACTCAGGGTTTC	12449
rs29499473	snp	C/T	0.375	0.216506	intron-variant	Ccnf	Mm_Celera	17:24246321	CAGACAACTTGGCAA[C/T]TGTGAAAGATTTCTG	12449
rs29500388	snp	A/G	0.375	0.216506	utr-variant-3-prime	Ccnf	GRCm38.p3	17:24223772	TGGTCACTGAGCTCA[A/G]TGTCCTGACAGCTTG	12449
rs29500670	snp	C/T	0.32	0.24	intron-variant	Ccnf	GRCm38.p3	17:24236826	AAACAATGGAAGATT[C/T]GTGACATCAAGTTTG	12449
rs29502478	snp	C/T	0.375	0.216506	intron-variant	Ccnf	Mm_Celera	17:24248612	TGATGGCAGTCCCAA[C/T]ACTCCAGAGGTAAAA	12449
rs29540104	snp	C/G	0	0	intron-variant, upstream-variant-2KB	Ccnf, Mir5134	GRCm38.p3	17:24236396	AAAAGTTGTATTTTA[C/G]CTTCAGAAATCGGAG	12449
rs33048445	snp	A/G	0.375	0.216506	intron-variant	Ccnf	Mm_Celera	17:24227049	ATGACTGCTTCATTC[A/G]GAGATGTCCAGAGTG	12449
rs33081401	snp	C/T	0.32	0.24	intron-variant, downstream-variant-500B	Ccnf, Mir5134	Mm_Celera	17:24234210	CTTCCTCGCAAAGGA[C/T]ACTGGGATTGAAATT	12449
rs33088667	snp	A/G	0.32	0.24	intron-variant, upstream-variant-2KB	Ccnf, Mir5134	Mm_Celera	17:24236553	ATTCAGGGCTAGTCT[A/G]AGCTACAACAGGACT	12449
rs33106953	snp	A/T	0.444444	0.157135	upstream-variant-2KB	Ccnf	Mm_Celera	17:24252569	TCAGTTGATCAGTTG[A/T]CTTTTTTTTTTTTTT	12449
rs33125495	snp	G/T	0.375	0.216506	intron-variant	Ccnf	GRCm38.p3	17:24238966	AAACCTCTGACAGTC[G/T]TAGACATGAACACAA	12449
rs33136780	snp	A/G	0.375	0.216506	upstream-variant-2KB	Ccnf	Mm_Celera	17:24252962	TTGTGACCTAGAAGT[A/G]TAAGACAAATAAATT	12449
rs33152038	snp	A/G	0.375	0.216506	downstream-variant-500B, upstream-variant-2KB	Ccnf, 1600002H07Rik	Mm_Celera	17:24222834	CAGGCTTCAGCAGAC[A/G]CCCCAGGTGTTGAGG	12449
rs33158489	snp	A/G	0.444444	0.157135	intron-variant	Ccnf	GRCm38.p3	17:24226938	TATCAACGGTCAGAC[A/G]GACAAAGGTCCATTG	12449
rs33169247	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Ccnf, Mir5134	Mm_Celera	17:24235753	TGCGCACAGAACCTC[C/T]GGAACCCACTCATCT	12449
rs33174569	snp	G/T	0.5	0	intron-variant	Ccnf	Mm_Celera	17:24239523	TAGGGGCCAGAGATA[G/T]CTCAGAGGTTTAGGA	12449
rs33180378	snp	G/T	0.375	0.216506	intron-variant	Ccnf	Mm_Celera	17:24248714	AAAAACCACTCTTGG[G/T]GCTGGAGAGATAGCA	12449
rs33221762	snp	A/G	0.375	0.216506	intron-variant	Ccnf	GRCm38.p3	17:24248874	TACTGCATGCACATG[A/G]TGTATACAAGTTATG	12449
rs33273241	snp	A/G	0.375	0.216506	intron-variant	Ccnf	Mm_Celera	17:24226992	TTGACCCAGAAATGG[A/G]ATACTCAATTGAGAA	12449
rs33278010	snp	C/T	0.32	0.24	synonymous-codon	Ccnf	GRCm38.p3	17:24231884	CACAGCCTCTCTAAT[C/T]GTCAGAATCTCTTTG	12449
rs33282036	snp	A/C	0.375	0.216506	intron-variant	Ccnf	GRCm38.p3	17:24227310	AACTCACTCTGTAGA[A/C]CTGGCTGGCTTTGAA	12449
rs33282352	snp	C/G	0.375	0.216506	intron-variant	Ccnf	Mm_Celera	17:24239935	GACATCTGTCAACAA[C/G]AGAAAGTTATCCTCA	12449
rs33286786	snp	A/G	0.375	0.216506	intron-variant	Ccnf	Mm_Celera	17:24239704	GACAAGCATATGTAT[A/G]TAAATAAGTAAAAAC	12449
rs33309135	snp	C/G	0.444444	0.157135	intron-variant	Ccnf	GRCm38.p3	17:24226953	AGACAAAGGTCCATT[C/G]AAACACCAACACACA	12449
rs33316055	snp	A/G	0.32	0.24	synonymous-codon	Ccnf	Mm_Celera	17:24231809	CCCTTCCAGGGCGGA[A/G]ATGATCTCCCCCATC	12449
rs33335541	snp	A/G	0.32	0.24	intron-variant	Ccnf	GRCm38.p3	17:24236610	CAAGTACAAGCACTG[A/G]CATTTGGATCCAGAA	12449
rs33348082	snp	A/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Ccnf, Mir5134	GRCm38.p3	17:24236014	CCAAAATTTTACTTG[A/T]AATTTCAGATGAAAG	12449
rs33352118	snp	C/T	0.375	0.216506	intron-variant	Ccnf	Mm_Celera	17:24246711	TTCATAGGAGAAAAA[C/T]GGATAAATAAAGGGA	12449
rs33359023	snp	A/T	0.375	0.216506	intron-variant	Ccnf	Mm_Celera	17:24246955	AAATTGCTAAATAAA[A/T]TTTGTCTGGTTTTGT	12449
rs33379980	snp	A/T	0.375	0.216506	intron-variant	Ccnf	Mm_Celera	17:24248936	AAAAAAAAAAAAGAT[A/T]AAACCACGCAATTCT	12449
rs33386536	snp	A/G	0.375	0.216506	intron-variant	Ccnf	GRCm38.p3	17:24246582	ATTCTGACACACAGC[A/G]TTTCCCTATTTCCCA	12449
rs33414417	snp	A/C	0.32	0.24	intron-variant	Ccnf	Mm_Celera	17:24244094	GGGGGTCTCAGACAG[A/C]GGGCCTGGTCACTGG	12449
rs33430360	snp	A/T	0.375	0.216506	intron-variant	Ccnf	GRCm38.p3	17:24239599	CACATCAGGTGGCTC[A/T]CAAGTGCCTGTAACT	12449
rs33464932	snp	A/G	0.444444	0.157135	intron-variant	Ccnf	Mm_Celera	17:24248525	ATTCTGGACTAAAAA[A/G]GCACTTCTGGACCAT	12449
rs33500352	snp	A/G	0.375	0.216506	intron-variant	Ccnf	Mm_Celera	17:24248582	AGGTAAGGAAGAGCC[A/G]GGTAAGATGGTCACT	12449
rs33516921	snp	A/G	0.375	0.216506	intron-variant	Ccnf	Mm_Celera	17:24239800	GTTTAAAGCCTAGGC[A/G]GTCCTGCCCCAAGGT	12449
rs33526137	snp	A/G	0.32	0.24	intron-variant, downstream-variant-500B	Ccnf, Mir5134	GRCm38.p3	17:24234125	CAGGCTCTGGGTCCC[A/G]AGACTGTGTGGGGGA	12449
rs33585643	snp	A/T	0.375	0.216506	intron-variant	Ccnf	GRCm38.p3	17:24248885	CATGGTGTATACAAG[A/T]TATGCAGGCAAAACA	12449
rs33594489	snp	C/G	0.444444	0.157135	intron-variant	Ccnf	GRCm38.p3	17:24230305	GACGACAGATTCAGA[C/G]TCGGACTCACCACTT	12449
rs33635863	snp	C/T	0.375	0.216506	intron-variant	Ccnf	Mm_Celera	17:24248548	TGGACCATGCTGAGC[C/T]AAGTAAGGCACTGTC	12449
rs33648783	snp	C/T	0	0	intron-variant, upstream-variant-2KB	Ccnf, Mir5134	Mm_Celera	17:24236394	CCAAAAGTTGTATTT[C/T]ACCTTCAGAAATCGG	12449
rs33658626	snp	C/T	0.375	0.216506	missense	Ccnf	Mm_Celera	17:24226749	CGGCCGTCAGAGAGA[C/T]TTGTCTGTAGTCTTT	12449
rs33664820	snp	C/T	0.375	0.216506	intron-variant	Ccnf	Mm_Celera	17:24246624	CAGCGTGAGTATAAA[C/T]TGCTATCTCCTTAGG	12449
rs33666307	snp	A/C	0.444444	0.157135	intron-variant	Ccnf	Mm_Celera	17:24239005	GACAAGAGATCAGCC[A/C]GGACCATCTGTTGAT	12449
rs33680096	snp	A/C	0.444444	0.157135	downstream-variant-500B	Ccnf	Mm_Celera	17:24223118	CAGATGACCCAGGCC[A/C]CGTTGACTTGGAGCT	12449
rs33685094	snp	C/T	0.444444	0.157135	intron-variant	Ccnf	Mm_Celera	17:24230292	TCCAGTGTTGAGAGA[C/T]GACAGATTCAGACTC	12449
rs33705056	snp	C/T	0.375	0.216506	intron-variant	Ccnf	Mm_Celera	17:24227002	AATGGGATACTCAAT[C/T]GAGAAGCCAGATTCA	12449
rs33886857	snp	A/G	0.375	0.216506	intron-variant	Ccnf	Mm_Celera	17:24227399	TCATAAAACTTAAAC[A/G]ATCAGAGTGGGTAGA	12449
rs45656682	snp	C/G			intron-variant	Ccnf	Mm_Celera	17:24250099	TTGACCAAGGGACTT[C/G]CATAGCATAGACTGG	12449
rs45682217	snp	A/G			intron-variant, upstream-variant-2KB	Ccnf, Mir6965	Mm_Celera	17:24242879	AGACCAGGGCAGGAC[A/G]GAAGCTCTTTCCTCA	12449
rs45709832	snp	C/T			intron-variant	Ccnf	GRCm38.p3	17:24231106	GAACTCAGAAATTCA[C/T]CTGCCCTTGACTCCC	12449
rs45791827	snp	A/T			intron-variant	Ccnf	Mm_Celera	17:24244005	GAAAATCCTATGCTG[A/T]GTTAGTTTCTCAGCT	12449
rs45830230	snp	C/T			intron-variant, upstream-variant-2KB	Ccnf, Mir6965	Mm_Celera	17:24242061	ACTTTAAACGGCCCA[C/T]GGAACGTGCTTCAGG	12449
rs45835889	snp	C/T			intron-variant, upstream-variant-2KB	Ccnf, Mir5134	GRCm38.p3	17:24234804	ATCTCAATCCCTGCT[C/T]ATAGGCAGTGGGTAC	12449
rs45856256	snp	C/G			intron-variant	Ccnf	GRCm38.p3	17:24236966	CATCAAATTACTAAA[C/G]AGCTCACCCGCTCAC	12449
rs45861457	snp	C/T			intron-variant	Ccnf	GRCm38.p3	17:24239391	TTGTGACAGCAGCAG[C/T]ACTGAGAATTAAGAG	12449
rs45867292	snp	A/T			intron-variant	Ccnf	GRCm38.p3	17:24238937	TGAGCCATCTTACTA[A/T]TAACATTTTCTGTAA	12449
rs45874666	snp	A/G			intron-variant	Ccnf	Mm_Celera	17:24232948	AGTACTAACAATCAG[A/G]AACACTCTGTTCCAG	12449
rs45884175	snp	C/T			intron-variant	Ccnf	Mm_Celera	17:24250259	GCAAAATCACCCCTT[C/T]CTAGCACCGTGGACC	12449
rs45910340	snp	A/G			intron-variant	Ccnf	Mm_Celera	17:24245438	CGCTCCAAAAACTGT[A/G]CAACAGTCCAAAGAT	12449
rs45945353	snp	A/G			intron-variant	Ccnf	Mm_Celera	17:24244702	TCAGCATGGTAAAGA[A/G]CTCAACTTCCATGTA	12449
rs45989186	snp	C/T			intron-variant, upstream-variant-2KB	Ccnf, Mir6965	Mm_Celera	17:24241692	CGGCCCCACTCAGGC[C/T]ATATTTATTTCATAT	12449
rs46051542	snp	A/G			intron-variant	Ccnf	Mm_Celera	17:24233110	GCCTATCTGAAGAAG[A/G]CCCGGGATGCGGTAA	12449
rs46075176	snp	A/G			intron-variant	Ccnf	Mm_Celera	17:24226930	CATGTGTCTATCAAC[A/G]GTCAGACGGACAAAG	12449
rs46104481	snp	C/G			intron-variant	Ccnf	Mm_Celera	17:24230691	AAATTAAATATAAAT[C/G]TAAAGTCAAGATAAA	12449
rs46141393	snp	G/T			intron-variant	Ccnf	Mm_Celera	17:24243157	TCCTTAGAACCTATA[G/T]CCAAGTGTCAAGGGC	12449
rs46159122	snp	A/T			intron-variant	Ccnf	Mm_Celera	17:24237977	GGACTCTCTCTGAGG[A/T]TCGTGCTCACGTGTC	12449
rs46279886	snp	A/G			intron-variant	Ccnf	Mm_Celera	17:24244622	TGTGAGAATCACTGA[A/G]GGACTTCCCAAATCC	12449
rs46339049	snp	A/G			intron-variant	Ccnf	Mm_Celera	17:24246986	TTAAAAACAAAATAA[A/G]ACAAACAACTATGAA	12449
rs46377222	snp	C/T			intron-variant	Ccnf	Mm_Celera	17:24245202	ACGGTGCTGACACTT[C/T]CAGGGATATGATAAC	12449
rs46396963	snp	A/G			intron-variant	Ccnf	GRCm38.p3	17:24236935	ATCAATCAATGTGGA[A/G]CGGAAATACTTTCTT	12449
rs46400275	snp	A/G			intron-variant	Ccnf	GRCm38.p3	17:24238516	GTTTGTCAAAGGGGT[A/G]AAGATCCACAGGCTG	12449
rs46474250	snp	A/C			intron-variant, upstream-variant-2KB	Ccnf, Mir6965	GRCm38.p3	17:24241160	CCTAGCCTACACCTG[A/C]AAAGGGACCCACAGA	12449
rs46519417	snp	A/G			intron-variant	Ccnf	GRCm38.p3	17:24232629	ACTGCATCTGAGTAC[A/G]AAGAATGCAAACATA	12449
rs46545142	snp	C/G			intron-variant	Ccnf	Mm_Celera	17:24226237	TCTCCCTGAAAGTAA[C/G]AGAGATAAAACAAGA	12449
rs46556986	snp	C/T			intron-variant	Ccnf	Mm_Celera	17:24232388	CATGGCACAGTCTAC[C/T]CTAGCTGTTCTCTCC	12449
rs46577676	snp	C/T			upstream-variant-2KB	Ccnf	Mm_Celera	17:24252629	TTTCAGTTTCTATTA[C/T]TTATTGGAGGCGGGT	12449
rs46587970	snp	A/G			intron-variant	Ccnf	Mm_Celera	17:24237633	AAATGGCGCATCGAT[A/G]GCCTTGGAGTCAGAT	12449
rs46698558	snp	A/C			intron-variant	Ccnf	Mm_Celera	17:24245217	TCAGGGATATGATAA[A/C]CTTGACGATACGTTT	12449
rs46712483	snp	A/G			intron-variant	Ccnf	Mm_Celera	17:24250024	TACTGCATTCTAAGT[A/G]TTAGTCACTATGGCC	12449

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