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
rs6224195	snp	A/G	0.5	0	intron-variant	Phf14	Mm_Celera	6:11959570	ATTTGCCATCAGTAG[A/G]AAACATTCAGACCCT	75725
rs6238110	snp	A/G	0.48	0.0979796	intron-variant	Phf14	Mm_Celera	6:12041245	ACAGACAGCTCAGGT[A/G]TTTGACAGTTAATTG	75725
rs6239240	snp	A/T	0.5	0	intron-variant	Phf14	Mm_Celera	6:12041493	AGAGGCCATATATCA[A/T]AAAAATGTGGTGGAG	75725
rs6239757	snp	A/G	0.5	0	intron-variant	Phf14	GRCm38.p3	6:12041582	cacacacacgcacac[A/G]cacacacacacacac	75725
rs6347458	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	Ndufa4, Phf14	Mm_Celera	6:11907145	ACCTTTCTCCCTGAT[C/G]TCTGCCACCTTCTGC	75725
rs6347510	snp	A/C	0.5	0	intron-variant, upstream-variant-2KB	Ndufa4, Phf14	Mm_Celera	6:11907181	GCAACCTCACCTCCA[A/C]CCCAGNTAGAGGCTT	75725
rs6347522	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	Ndufa4, Phf14	Mm_Celera	6:11907187	TCACCTCCANCCCAG[C/G]TAGAGGCTTCAAGCA	75725
rs6347574	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Ndufa4, Phf14	Mm_Celera	6:11907219	TCAGGTCATCCCAAC[A/G]ACAGAATGTAACCCC	75725
rs6357013	snp	A/G	0.5	0	intron-variant	Phf14	Mm_Celera	6:12094120	CTCTGAGCTACACTC[A/G]GTGTGATGTGCTGCC	75725
rs6357497	snp	A/G	0.5	0	intron-variant	Phf14	Mm_Celera	6:12094201	TAATGAATGTTCTAA[A/G]TGGTGATAGAAGAGG	75725
rs6357570	snp	C/T	0.5	0	intron-variant	Phf14	Mm_Celera	6:12094253	CTAAATAAGCTTAGG[C/T]TTCAGGACAAGAATC	75725
rs6360634	snp	A/G	0.5	0	utr-variant-5-prime, upstream-variant-2KB	Ndufa4, Phf14	Mm_Celera	6:11907414	AAGATTAGGACACAC[A/G]CTAAGCCGCTTCTGC	75725
rs6382415	snp	C/T	0.5	0	intron-variant	Phf14	Mm_Celera	6:11914500	ACCTAAGGGCTTATT[C/T]TCAACAAGTATGTAA	75725
rs6383530	snp	A/G	0.5	0	intron-variant	Phf14	Mm_Celera	6:11914712	ttgagaacTTCTCTA[A/G]AGACTACGAGCAAAT	75725
rs6384149	snp	G/T	0.290657	0.246672	intron-variant	Phf14	Mm_Celera	6:11914812	AGAGAAGCTGACCTC[G/T]TAAGCTGCATAGTTG	75725
rs6384628	snp	A/C	0.290657	0.246672	intron-variant	Phf14	Mm_Celera	6:11914836	ATAGTTGTGTGGTTA[A/C]ATATTTATTATTTTG	75725
rs6384755	snp	A/C	0.5	0	intron-variant	Phf14	Mm_Celera	6:11914915	GTCAGCAGAGGAGTC[A/C]GTTGGGAAAAGAAGA	75725
rs29825809	snp	G/T	0.32	0.24	intron-variant	Phf14	Mm_Celera	6:11935212	ATTCTTATCTTTAGG[G/T]AAAGGAAAACTCATT	75725
rs29828062	snp	A/G	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12026548	CAATTCAAATGCTAC[A/G]TTCCTTGCCTTATGT	75725
rs29828134	snp	A/T	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12044121	AAACTCTCTTATACA[A/T]TTCTTTTCATTGTGG	75725
rs29829988	snp	A/G	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12019894	CTCTGAACCCTCATA[A/G]AAAAGCTGTGCATAG	75725
rs29872812	snp	A/C	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12078832	AGTTTCAGGAAAACT[A/C]ACACCCTCTTCTGTA	75725
rs29873254	snp	A/G	0.432133	0.171253	intron-variant	Phf14	Mm_Celera	6:12057793	GTTGGCCAGTTTAGT[A/G]ACTTTATTAGTTGAG	75725
rs29874037	snp	C/T	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12055563	GAGCCACCTGTCTTT[C/T]TCTCCTCTTCCTCTC	75725
rs29876496	snp	C/G	0.475309	0.108333	intron-variant	Phf14	Mm_Celera	6:12017539	AATAGAAGGACTTAG[C/G]TTGTTCTTAGAGATC	75725
rs29876779	snp	G/T	0.484429	0.0868505	intron-variant	Phf14	Mm_Celera	6:12014114	TGGAGGATTACTGTT[G/T]TAGTAGAGGTGGGTC	75725
rs29877478	snp	A/G	0.444444	0.157135	intron-variant	Phf14	Mm_Celera	6:12085484	AAGCTAGAGACAGTT[A/G]TGTGCTGTCCAACAT	75725
rs29879141	snp	A/C	0.444444	0.157135	intron-variant	Phf14	Mm_Celera	6:12019982	AGCCAGTTTAGCCAA[A/C]TCAATGAGCTCCACA	75725
rs29883523	snp	C/T	0.465374	0.126941	intron-variant	Phf14	Mm_Celera	6:12061028	GTGGAGTATAATCTG[C/T]GACTGACCCTATCCA	75725
rs29920988	snp	C/T	0.48	0.0979796	intron-variant, downstream-variant-500B	Phf14	Mm_Celera	6:12081534	CTAAGTAGAAAAGGG[C/T]TTTGTTGTTGTCCTC	75725
rs29922374	snp	A/C	0.32	0.24	intron-variant	Phf14	Mm_Celera	6:12022746	GTATACGTGTGTACA[A/C]ATGGATGTGTAAATG	75725
rs29923961	snp	A/G	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12054764	AGTTACAGCTGTTTG[A/G]GGGTTTGTTGTTGTT	75725
rs29923995	snp	A/T	0.444444	0.157135	intron-variant	Phf14	Mm_Celera	6:12013568	AGTCACTGTGTTATT[A/T]TTTGGTTTTACTTTA	75725
rs29924927	snp	C/T	0.33241	0.236027	intron-variant	Phf14	Mm_Celera	6:12055769	TAGCAATGGCATTGC[C/T]TCAGCTCTGGTAGAG	75725
rs29925607	snp	A/T	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12069807	ATCTAAAAATAAAAA[A/T]TGGAAAGTTTCAGAA	75725
rs29927002	snp	C/G	0.32	0.24	intron-variant, utr-variant-3-prime	Phf14	Mm_Celera	6:12040118	ATTTTACTTGTTGAA[C/G]CTAAATGTGAAGCTA	75725
rs29930528	snp	C/T	0.32	0.24	intron-variant	Phf14	Mm_Celera	6:12068810	TATTTATGAAGTAGA[C/T]CTCTTATATCAGGAT	75725
rs29961451	snp	C/G	0.429688	0.173817	intron-variant	Phf14	Mm_Celera	6:12035565	AAGATTTTTAAAAAT[C/G]TAGACGCTTATATAT	75725
rs29971659	snp	A/C	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12057417	TTTTTTTGAGGCAGT[A/C]TGTCATTTGGCTTGG	75725
rs29972325	snp	C/T	0.493827	0.0552116	intron-variant	Phf14	Mm_Celera	6:12077114	TCACTCTTTTCCACC[C/T]AGAGTACTAGACCAT	75725
rs29973990	snp	A/G	0.33241	0.236027	intron-variant	Phf14	Mm_Celera	6:12051405	CTGTACCATGCTGTG[A/G]ATGCCACATGTGACA	75725
rs29975697	snp	A/G	0.475309	0.108333	intron-variant	Phf14	Mm_Celera	6:12017012	CATCGTCTAAGAGAC[A/G]GATGCCTGTTAGCTT	75725
rs29977575	snp	A/G	0.32	0.24	intron-variant	Phf14	Mm_Celera	6:12021730	AGTAATACGTCATAA[A/G]CTTGGTACCAGTTTA	75725
rs29982279	snp	C/T	0.46875	0.121031	intron-variant	Phf14	Mm_Celera	6:12058639	CTTTTCCTTGTCCTT[C/T]GAAGGCTATTTAAAT	75725
rs30011241	snp	C/T	0.290657	0.246672	intron-variant	Phf14	Mm_Celera	6:12034792	CCTTGCCGTGCCTCA[C/T]CAGACATGCAGTGCC	75725
rs30022344	snp	A/C	0.32	0.24	intron-variant	Phf14	Mm_Celera	6:12068662	GCACCTTGAACTTAG[A/C]TATAATAATCCCAGC	75725
rs30024040	snp	A/G	0.493827	0.0552116	intron-variant	Phf14	Mm_Celera	6:12077354	ATTAAGAGCATGCCT[A/G]TGTGCATTCCAGTAC	75725
rs30060707	snp	G/T	0.277778	0.248452	intron-variant	Phf14	Mm_Celera	6:12037783	CTTAGTAGTAATGAT[G/T]CAGTAATGATTAATC	75725
rs30066659	snp	G/T	0.444444	0.157135	intron-variant, utr-variant-3-prime	Phf14	Mm_Celera	6:12040601	ATTTATTGATTTTAT[G/T]GCACTAGAAAAAATA	75725
rs30067515	snp	G/T	0.345679	0.230967	intron-variant	Phf14	Mm_Celera	6:12017210	TATGCAATACCTAGT[G/T]GTGTGACCTGTCACA	75725
rs30073446	snp	G/T	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12026708	AGAGGTTTATTTTCT[G/T]GTGTGTGGAGCAGGG	75725
rs30074804	snp	G/T	0.444444	0.157135	intron-variant	Phf14	Mm_Celera	6:12035711	GTTGTTGTTGTTGTT[G/T]TTGTTTTTGTTTTGA	75725
rs30113390	snp	C/T	0.32	0.24	intron-variant	Phf14	Mm_Celera	6:12068127	TAATTAGCTACAGGG[C/T]CCTGGGGAAATCAGT	75725
rs30115135	snp	C/T	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12078116	GTCATAGTGATGCCT[C/T]AGCTTCCAGACGTAT	75725
rs30116985	snp	C/T	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12043278	GTTATCAATATCCAT[C/T]TGTAATGAGGAATTT	75725
rs30117474	snp	C/G	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12082291	TTATAGAAGACTGGA[C/G]TTTGGCTTCTAGCAT	75725
rs30121353	snp	A/C/T	0.375	0.216506	intron-variant	Phf14	GRCm38.p3	6:12076333	TGTATAACCACTGTA[A/C/T]AATTTCCAGAACCAG	75725
rs30123599	snp	A/G	0.375	0.216506	intron-variant	Phf14	GRCm38.p3	6:12021979	TGTGTGTGTGTGTGC[A/G]TGTTCTACCTAGCTT	75725
rs30124635	snp	G/T	0.32	0.24	intron-variant	Phf14	Mm_Celera	6:12030172	CTAGCATTACCGCAA[G/T]ATCTTTTCTATTATT	75725
rs30124920	snp	A/T	0.492188	0.0620098	intron-variant	Phf14	Mm_Celera	6:12014068	GATCAAATGTCCCTC[A/T]CAAAAGTTGGTCTCT	75725
rs30125234	snp	C/G	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12069504	TTCCCCTCTGAAAAC[C/G]CCCTATCCCCTCCCC	75725
rs30163992	snp	A/G	0.455	0.143091	intron-variant	Phf14	Mm_Celera	6:12026486	ACATCTGCTTGAAAA[A/G]GCCCATCTTCCTTCC	75725
rs30164759	snp	C/G	0.444444	0.157135	intron-variant	Phf14	Mm_Celera	6:12018573	AGATACCATAGAGAC[C/G]CACATGGAGACTGAC	75725
rs30165336	snp	G/T	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12034492	AGATTGCATCTTTCT[G/T]CTGTAAGAAGAGCTC	75725
rs30168601	snp	A/G	0.492188	0.0620098	intron-variant	Phf14	Mm_Celera	6:12013088	AAGTAATGAATTCAG[A/G]CTTGTACCATCTCAC	75725
rs30169863	snp	A/G	0.345679	0.230967	intron-variant	Phf14	Mm_Celera	6:12053058	ATCTGTAATCTGAGT[A/G]CCCCTACAGTCAGGT	75725
rs30169896	snp	A/T	0.375	0.216506	intron-variant, downstream-variant-500B	Phf14	Mm_Celera	6:12081466	CTCAAATGTTTTTTT[A/T]AAAGAAAGAAATTGT	75725
rs30208393	snp	A/C	0.401235	0.199068	intron-variant	Phf14	Mm_Celera	6:12062286	CTCAGGGTTTCCAGC[A/C]ATGCACTGACGCGTT	75725
rs30211786	snp	C/G	0.391111	0.206368	intron-variant	Phf14	Mm_Celera	6:12036016	ATCGATATTTATATT[C/G]TTCATGTAGCAAAAG	75725
rs30216666	snp	G/T	0.387812	0.208586	intron-variant	Phf14	Mm_Celera	6:12027162	GGTAACTAACTCATA[G/T]TCTTCAGGTCCTGTC	75725
rs30253579	snp	A/G	0.444444	0.157135	intron-variant	Phf14	Mm_Celera	6:12063697	CTGGAATAGTTATGT[A/G]TAGTTCATTGTTTTC	75725
rs30263542	snp	G/T	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12051999	TCCCTCCCATTTTGG[G/T]GGGTATTTCAGCTAA	75725
rs30266356	snp	G/T	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12036113	AGTTCCAATCCTCAG[G/T]TCCCATATATAAATT	75725
rs30267271	snp	A/G	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12027041	ACCCCAGGCAGGAGG[A/G]GAGAGCTGTAAGGAG	75725
rs30267463	snp	A/G	0.5	0	intron-variant	Phf14	Mm_Celera	6:12074011	ACTGTTGAGTGTTTA[A/G]TGACTTACTAGATTG	75725
rs30267608	snp	A/G	0.345679	0.230967	intron-variant	Phf14	Mm_Celera	6:12064925	TATGCTAAAATAAAA[A/G]TTTGGTTAAATACAG	75725
rs30268190	snp	A/G	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12019938	TAATTATGTGCTGGA[A/G]ACAGGAGAGTCCTGG	75725
rs30271417	snp	A/G	0.5	0	intron-variant	Phf14	Mm_Celera	6:12065980	ACATCTTTAATTATA[A/G]TCTCTTTAATTTTTT	75725
rs30313504	snp	A/G	0	0	intron-variant	Phf14	Mm_Celera	6:12042841	ATTGACCTCCTAGCC[A/G]TTATCTCCTTTATCT	75725
rs30313724	snp	A/G	0.32	0.24	intron-variant	Phf14	Mm_Celera	6:12068661	TGCACCTTGAACTTA[A/G]CTATAATAATCCCAG	75725
rs30314559	snp	A/T	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12082382	TATACACACATGCAC[A/T]CATGCATACACATGC	75725
rs30317417	snp	A/G	0	0	intron-variant	Phf14	Mm_Celera	6:12042658	TAAGGAATGCGAACA[A/G]AGACGGGATTTACAA	75725
rs30317587	snp	C/T	0.32	0.24	intron-variant	Phf14	Mm_Celera	6:12021168	AACTGCTACTGAGGC[C/T]GCACCTTTACCAACC	75725
rs30317897	snp	C/G	0.32	0.24	intron-variant, utr-variant-3-prime	Phf14	Mm_Celera	6:12039736	GCCAGTGGGACTTAC[C/G]TGCTCTGTGCTACCC	75725
rs30319449	snp	A/G	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:11918766	ACCATGGATATATGA[A/G]AAACTGTCTCCAAAG	75725
rs30326000	snp	C/T	0.444444	0.157135	intron-variant	Phf14	Mm_Celera	6:12016905	AAAGTATGATGCAGA[C/T]CACGCCTGTTTCCTG	75725
rs30351621	snp	C/T	0.391111	0.206368	intron-variant	Phf14	Mm_Celera	6:12015504	GACTTCACAGATGGG[C/T]TTTTGTTTTTTCTCA	75725
rs30361253	snp	C/T	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12083362	CCTACACTAGGACAT[C/T]GACATCGAACCGCCT	75725
rs30361883	snp	C/T	0.444444	0.157135	intron-variant	Phf14	Mm_Celera	6:12016797	AATCATTGTCTTAAT[C/T]TTATTGTCCAAGTTA	75725
rs30363804	snp	A/G	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12066870	ATGGCTGCTGGGAGT[A/G]CAAACTTGTACAGAC	75725
rs30364914	snp	C/T	0.5	0	intron-variant	Phf14	Mm_Celera	6:12025242	TTGAGGTCCTTGATC[C/T]ACTTGGACTTGAGCT	75725
rs30365581	snp	C/T	0.46875	0.121031	intron-variant	Phf14	Mm_Celera	6:12038499	TTCGTGGTCTGTGGT[C/T]GAGTTTGGCGTGGTA	75725
rs30368219	snp	C/T	0.444444	0.157135	intron-variant	Phf14	Mm_Celera	6:12024283	CCAGAGGCCTCCAGT[C/T]TCTTAAGGGTTAAGT	75725
rs30369567	snp	C/T	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12055602	CTTCTGTTTCATTCT[C/T]TTCCCTATCTCTCAC	75725
rs30369777	snp	A/G	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12050931	ACAATAACAACGGCT[A/G]TTGTATATTGTTACT	75725
rs30411749	snp	C/T	0.455	0.143091	intron-variant	Phf14	Mm_Celera	6:12051496	GCCTTTGAAAAGTTG[C/T]CAGCATCCTTCTGCC	75725
rs30412208	snp	G/T	0.465374	0.126941	intron-variant	Phf14	Mm_Celera	6:12088419	GGGTTTGGAAAGTTT[G/T]TGAGGGGAGAGCAGA	75725
rs30416908	snp	C/T	0.345679	0.230967	intron-variant	Phf14	Mm_Celera	6:12072216	TAGCCCATCATGTGG[C/T]GTTAGTCTTAATAAA	75725
rs30418132	snp	C/T	0.375	0.216506	intron-variant	Phf14	Mm_Celera	6:12052136	GTTCAATTTCCTGAC[C/T]GTCCGTGCATCTCCC	75725
rs30418275	snp	G/T	0.489796	0.070696	intron-variant	Phf14	Mm_Celera	6:12075780	AGCATAGCACGGTTA[G/T]GAAAGTAAAAGCCAC	75725

Full records

It may take some time, please wait.