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
rs6370710	snp	A/T	0.5	0	intron-variant	Gtf2h2	Mm_Celera	13:100466190	ctgactccatgatag[A/T]agtgccattcgggtc	23894
rs13466278	snp	G/T	0.497778	0.0332592	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	Gtf2h2	GRCm38.p3	13:100492489	GGCTGGAGTGAGGCG[G/T]ACAGGAGAAGAAGCC	23894
rs29228276	snp	C/G	0.375	0.216506	intron-variant	Gtf2h2	GRCm38.p3	13:100464072	AAGTGCCTGCATCTA[C/G]TCACAGCTTGAGGCC	23894
rs29229040	snp	A/G	0.429688	0.173817	intron-variant	Gtf2h2	GRCm38.p3	13:100483681	GTATTTTTCTTGGGG[A/G]AAGCAAACAAGAACT	23894
rs29229155	snp	A/G/T	0.49827	0.0293608	intron-variant	Gtf2h2	GRCm38.p3	13:100485514	TCATTTAAGGAATAG[A/G/T]CTATTTTACAAAAAG	23894
rs29230283	snp	C/T	0.493827	0.0552116	upstream-variant-2KB	Gtf2h2	Mm_Celera	13:100493916	GTAGTCTCAGTATAA[C/T]TATGACTAATATTCC	23894
rs29232899	snp	G/T	0.375	0.216506	upstream-variant-2KB	Gtf2h2	GRCm38.p3	13:100493840	TGCTGGAACAGGGGG[G/T]TTTTATTAAAACTTT	23894
rs29233052	snp	C/G	0.444444	0.157135	intron-variant	Gtf2h2	GRCm38.p3	13:100473074	TTCCTGGCAGAGGCA[C/G]GCAGATCTCTAAGCT	23894
rs29238759	snp	C/T	0.429688	0.173817	intron-variant	Gtf2h2	GRCm38.p3	13:100487566	ATAAACCAAGACAAC[C/T]ACTTTTTCAAGTTCT	23894
rs29239067	snp	C/T	0.493827	0.0552116	intron-variant	Gtf2h2	Mm_Celera	13:100464894	TTATGCTGAGAAACA[C/T]ACCCAGCTTCTACTT	23894
rs29241000	snp	C/T	0.375	0.216506	intron-variant	Gtf2h2	GRCm38.p3	13:100480792	CTCAATGTCTCTAGA[C/T]ATAATAGTAACAAAA	23894
rs29242052	snp	A/G	0.484429	0.0868505	intron-variant	Gtf2h2	GRCm38.p3	13:100487037	AAACCAAAAAAATTA[A/G]TGGATCCATTTGGAG	23894
rs29242782	snp	A/T	0.375	0.216506	intron-variant	Gtf2h2	Mm_Celera	13:100463959	GACAGACAGACAGAC[A/T]GACTGACTATTTTTC	23894
rs29244850	snp	C/T	0.493827	0.0552116	intron-variant, nc-transcript-variant	Gtf2h2	GRCm38.p3	13:100461929	CAGGATGCTGCTTCA[C/T]GGTGTAAATTTTCTA	23894
rs29246967	snp	C/T	0.444444	0.157135	upstream-variant-2KB	Gtf2h2	GRCm38.p3	13:100494114	TGGCCTGGGCTGTAT[C/T]ATAAGACCTCGTGTA	23894
rs29247358	snp	G/T	0.5	0	intron-variant	Gtf2h2	GRCm38.p3	13:100487793	GTGTTGGACTTTCTA[G/T]AACAGGAGTTCCTGA	23894
rs29495269	snp	A/G	0.444444	0.157135	intron-variant	Gtf2h2	Mm_Celera	13:100491694	TGGAGCACACCTTTA[A/G]TCCCAGCACTCGGAA	23894
rs29495560	snp	A/T	0.375	0.216506	intron-variant	Gtf2h2	GRCm38.p3	13:100480804	AGATATAATAGTAAC[A/T]AAAAAATTAAAGCCA	23894
rs29509999	snp	A/T	0.493827	0.0552116	intron-variant	Gtf2h2	GRCm38.p3	13:100461413	GCTCCTCCCTTGGAT[A/T]AATGCCATCGCCATT	23894
rs29511010	snp	A/T	0.375	0.216506	intron-variant	Gtf2h2	GRCm38.p3	13:100488343	TTATACAATCCCTGG[A/T]TCACCCAGAACAAAG	23894
rs29511395	snp	C/T	0.493827	0.0552116	intron-variant	Gtf2h2	GRCm38.p3	13:100486361	TACCAAAAATAGGTA[C/T]ATAATCTGGTTCCCT	23894
rs29516623	snp	A/G	0.5	0	upstream-variant-2KB	Gtf2h2	GRCm38.p3	13:100494192	TGTGTGTGTGTCCAT[A/G]GCTGGCTGGCACAAT	23894
rs29528018	snp	A/C	0.444444	0.157135	intron-variant	Gtf2h2	Mm_Celera	13:100491779	TTCCAGGACTGCCAA[A/C]ACTACACAGAGAAAC	23894
rs29534817	snp	G/T	0.375	0.216506	intron-variant	Gtf2h2	GRCm38.p3	13:100485153	CACTGTGGCAGTGGG[G/T]TTTGAGGTCTTCTCT	23894
rs29548950	snp	C/G	0.444444	0.157135	intron-variant	Gtf2h2	Mm_Celera	13:100460679	ACATCGTGTCTCTCT[C/G]TGTGTGTGTGTGTGT	23894
rs29549238	snp	A/T	0.5	0	intron-variant	Gtf2h2	GRCm38.p3	13:100473254	CTTTAACATTTTTTT[A/T]AAAAGATAGCTCAGC	23894
rs29570180	snp	C/G	0.375	0.216506	intron-variant	Gtf2h2	Mm_Celera	13:100480718	CTACCAAAGTTTCTA[C/G]AGATGAAAATATATA	23894
rs29582841	snp	A/G	0.493827	0.0552116	intron-variant	Gtf2h2	GRCm38.p3	13:100461201	TAAAGCCAACCCATA[A/G]TTTTCCTTATTTTAA	23894
rs29626228	snp	C/T	0.32	0.24	intron-variant	Gtf2h2	GRCm38.p3	13:100465336	ACATCTATACATGAC[C/T]ACAGGGCAAGCTGAT	23894
rs29721134	snp	C/T	0.444444	0.157135	intron-variant	Gtf2h2	GRCm38.p3	13:100487488	GGGGTCACCACAACA[C/T]GAGGAACTGTATTAA	23894
rs29725123	snp	A/G	0.375	0.216506	intron-variant, downstream-variant-500B	Gtf2h2	Mm_Celera	13:100476150	CATAGAATCTCCTAG[A/G]GCTGGAAGTGCAGGC	23894
rs29725922	snp	C/T	0.493827	0.0552116	downstream-variant-500B, nc-transcript-variant	Gtf2h2	GRCm38.p3	13:100459987	TTTAACACCACTTTC[C/T]TAAGCAAGATGTGTA	23894
rs29762567	snp	A/G	0.444444	0.157135	intron-variant	Gtf2h2	Mm_Celera	13:100491852	TTTCTGTTCAGGATG[A/G]GCATAGTGGAATACA	23894
rs29776868	snp	A/G	0.444444	0.157135	intron-variant	Gtf2h2	Mm_Celera	13:100472670	GCGGTGGTGGCGCAT[A/G]CCTTTAATCCCAGCA	23894
rs29777127	snp	A/C	0.487535	0.077957	downstream-variant-500B	Gtf2h2	GRCm38.p3	13:100459707	CGCCTCGAGTTTTGA[A/C]GTAATGTTTTTTTTG	23894
rs29804283	snp	G/T	0.375	0.216506	intron-variant	Gtf2h2	Mm_Celera	13:100491856	TGTTCAGGATGGGCA[G/T]AGTGGAATACACCTG	23894
rs29806169	snp	A/T	0.375	0.216506	intron-variant	Gtf2h2	GRCm38.p3	13:100477363	CAGCCAGGACTACAC[A/T]GTAGTACCCTGTCTC	23894
rs29829638	snp	C/G	0.493827	0.0552116	downstream-variant-500B	Gtf2h2	GRCm38.p3	13:100459570	ACTGGAGCCACAGAC[C/G]AGGGTCTGAGGTAAA	23894
rs29858779	snp	C/T	0.493827	0.0552116	intron-variant	Gtf2h2	GRCm38.p3	13:100461524	GTATCCCTACTGCTT[C/T]AACTCTTGATGTACA	23894
rs29859613	snp	G/T	0.444444	0.157135	intron-variant	Gtf2h2	GRCm38.p3	13:100472904	GATGCCTGTGGCTTT[G/T]TTTTTTCAGGACGGG	23894
rs29864172	snp	A/T	0.444444	0.157135	intron-variant	Gtf2h2	GRCm38.p3	13:100487500	ACACGAGGAACTGTA[A/T]TAAAAGTTCACAGCA	23894
rs29865345	snp	A/G	0.456747	0.140554	intron-variant	Gtf2h2	GRCm38.p3	13:100487914	CAAACCTTAAAGCAC[A/G]GAGCCATCCTGTCAG	23894
rs29897091	snp	C/T	0.5	0	intron-variant	Gtf2h2	GRCm38.p3	13:100477992	ACTACCACCCATCTT[C/T]CTTCTTCCTCCTCTC	23894
rs29910570	snp	C/T	0.375	0.216506	intron-variant	Gtf2h2	GRCm38.p3	13:100463008	CCTTTCGTCAGCCAT[C/T]ATCCTTTTCTGGATG	23894
rs29956618	snp	A/G	0.444444	0.157135	intron-variant	Gtf2h2	GRCm38.p3	13:100472855	ACGGTATGTACCCTA[A/G]ATGAGTACACCAAGG	23894
rs29959104	snp	C/T	0.487535	0.077957	intron-variant	Gtf2h2	GRCm38.p3	13:100462801	AACTGGAGGCAACTG[C/T]CTTGTCTCAGCTTTC	23894
rs29962375	snp	A/T	0.444444	0.157135	upstream-variant-2KB	Gtf2h2	GRCm38.p3	13:100494452	GTTAAAAAAGATTTA[A/T]TTAGGGCTGGTGAGA	23894
rs30011036	snp	A/T	0.32	0.24	intron-variant	Gtf2h2	GRCm38.p3	13:100470571	CTCACTCTGTAGACC[A/T]GGCTGGCCTCGAACT	23894
rs30011550	snp	A/G	0.487535	0.077957	intron-variant	Gtf2h2	GRCm38.p3	13:100492094	ACCGGGGAGAAGTTA[A/G]AAGTCCCCACGCCGC	23894
rs30065524	snp	C/G	0.444444	0.157135	intron-variant	Gtf2h2	Mm_Celera	13:100460677	TAACATCGTGTCTCT[C/G]TCTGTGTGTGTGTGT	23894
rs30079034	snp	A/G	0.32	0.24	intron-variant	Gtf2h2	GRCm38.p3	13:100466938	AGAGACATTTCCCAC[A/G]TTTACTATTGCTTTA	23894
rs30093608	snp	A/G	0.487535	0.077957	intron-variant	Gtf2h2	GRCm38.p3	13:100484359	CTGACATCTCGACAA[A/G]AAATTTGATGACAAG	23894
rs45632553	snp	C/G			intron-variant	Gtf2h2	Mm_Celera	13:100471600	CGCCTCAGCTCCAAA[C/G]TTTGTCTCTGTAACT	23894
rs45784298	snp	A/G	0.132653	0.220748	intron-variant	Gtf2h2	Mm_Celera	13:100465446	TGAAATGCTAAGTTT[A/G]GTTGATATACATAGG	23894
rs45862824	snp	A/C	0.444444	0.157135	intron-variant	Gtf2h2	GRCm38.p3	13:100486437	TATATTTGACAGCAA[A/C]ATAGGAATCTAGTTC	23894
rs45923861	snp	A/G	0.459184	0.136902	intron-variant	Gtf2h2	GRCm38.p3	13:100490656	TTCCTATCTGAAACC[A/G]CAGACAGGGAACTAA	23894
rs46107415	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100491796	CTACACAGAGAAACC[A/G]TCTCCAAATTAATTA	23894
rs46139245	snp	A/G			downstream-variant-500B, nc-transcript-variant	Gtf2h2	Mm_Celera	13:100459943	GCTCTTAACCAATGA[A/G]CCATCTCTCCAGCCC	23894
rs46287394	snp	C/T	0.124444	0.216185	intron-variant	Gtf2h2	Mm_Celera	13:100461352	AAGTGGTGACCCATA[C/T]CTTCAACAATTTCCC	23894
rs46311585	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100471586	ATGGTCCATCCTTTC[A/G]CCTCAGCTCCAAACT	23894
rs46476130	snp	C/T			intron-variant	Gtf2h2	Mm_Celera	13:100471916	TCTGTATCCATTTCT[C/T]TGTTGAGGAACATCT	23894
rs46513567	snp	A/G	0.497778	0.0332592	intron-variant	Gtf2h2	GRCm38.p3	13:100490672	CAGACAGGGAACTAA[A/G]GCCAGAACGTTATTC	23894
rs46547215	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100474334	CTCCCTGAAACAGAC[A/G]TCATCATCATCTCCA	23894
rs46576434	snp	A/C	0.297521	0.245442	intron-variant	Gtf2h2	GRCm38.p3	13:100467552	ATGTGCATAAAAATG[A/C]TTTCAAGAGTTAAAT	23894
rs46582440	snp	G/T	0.444444	0.157135	intron-variant	Gtf2h2	Mm_Celera	13:100486785	GATTGTAGGTATGTA[G/T]GTAACTCCAGCTCTC	23894
rs46608877	snp	A/C	0.396694	0.202437	intron-variant	Gtf2h2	GRCm38.p3	13:100490279	CAGTGTATTCAGTAA[A/C]TATTCTATGAAAATA	23894
rs46638226	snp	C/T	0.124444	0.216185	intron-variant	Gtf2h2	GRCm38.p3	13:100462870	ATCATCTTTTATTTA[C/T]CTTTTCCCTACAGCA	23894
rs46762020	snp	A/G	0.142012	0.225474	intron-variant	Gtf2h2	Mm_Celera	13:100472917	TTGTTTTTTCAGGAC[A/G]GGCTGGTATATACCT	23894
rs46825392	snp	C/T	0.124444	0.216185	intron-variant	Gtf2h2	Mm_Celera	13:100484138	GTACCAACACCCAAA[C/T]GTCAGTCTCCTGGTT	23894
rs46866097	snp	A/C/T	0.132653	0.220748	intron-variant	Gtf2h2	Mm_Celera	13:100464295	AGGAAAAATTTAGAA[A/C/T]GTTTAAAAATACAAT	23894
rs46893124	snp	C/T	0.124444	0.216185	upstream-variant-2KB	Gtf2h2	Mm_Celera	13:100493926	TATAACTATGACTAA[C/T]ATTCCAATCACATAT	23894
rs46983253	snp	C/T	0.459184	0.136902	intron-variant	Gtf2h2	GRCm38.p3	13:100485886	GATGAAGAATGTGTA[C/T]TTAAATAAGCATATT	23894
rs46993797	snp	A/T			intron-variant	Gtf2h2	Mm_Celera	13:100467553	TGTGCATAAAAATGA[A/T]TTCAAGAGTTAAATA	23894
rs47059268	snp	G/T			upstream-variant-2KB	Gtf2h2	Mm_Celera	13:100493251	AGACGAAGGGCACCA[G/T]TCTCTGACTTTTTTT	23894
rs47090194	snp	A/T			intron-variant	Gtf2h2	GRCm38.p3	13:100471656	TTCTAAGAAGGGGCA[A/T]AGTGTCCACACTTCG	23894
rs47137869	snp	C/T	0.124444	0.216185	intron-variant	Gtf2h2	Mm_Celera	13:100488664	AGCTGTGTCCAGATA[C/T]AACCAGCAGAGAGGC	23894
rs47172508	snp	A/G	0.132653	0.220748	downstream-variant-500B, intron-variant	Gtf2h2	Mm_Celera	13:100468099	TGTGGATGACTTGGT[A/G]GCTGAAATCACTCCA	23894
rs47243128	snp	C/T	0.32	0.24	intron-variant	Gtf2h2	Mm_Celera	13:100489403	AGTTAAAAAGAAATA[C/T]GAAGGACGGTCACAG	23894
rs47267312	snp	A/G	0.124444	0.216185	intron-variant	Gtf2h2	Mm_Celera	13:100461602	TGTTTCTAGGATCCT[A/G]CTGTGAGGTGTGACT	23894
rs47473006	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100486400	CAAAGAATATATGTC[C/T]CATTTTAAAAGAAAA	23894
rs47501953	snp	C/T	0.124444	0.216185	intron-variant	Gtf2h2	Mm_Celera	13:100461709	AATGAGTCCTCTGTC[C/T]TGTAAATCTGAACCC	23894
rs47522121	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100491577	GGGGTAGGAAATAGG[A/G]GGTTTTCGGAGGGGA	23894
rs47535026	snp	C/T	0.124444	0.216185	upstream-variant-2KB	Gtf2h2	Mm_Celera	13:100492710	AGTGGTGCCCAAGAG[C/T]GTAACTGCCTTCCAG	23894
rs47765990	snp	C/T	0.132653	0.220748	downstream-variant-500B, intron-variant	Gtf2h2	Mm_Celera	13:100468120	AATCACTCCAAAAGG[C/T]AGAGCCCTGGTACCT	23894
rs47811480	snp	A/G	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Gtf2h2	Mm_Celera	13:100468952	AATACAGCCAGGACA[A/G]CAATGGAGAGAGTCA	23894
rs48038280	snp	A/C	0.152778	0.230321	intron-variant	Gtf2h2	Mm_Celera	13:100483401	CATATCCATTAATAT[A/C]CACTTAAAATGAATA	23894
rs48053410	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100471655	ATTCTAAGAAGGGGC[A/G]TAGTGTCCACACTTC	23894
rs48078881	snp	G/T	0.497778	0.0332592	intron-variant	Gtf2h2	GRCm38.p3	13:100490827	CTGATGGGAGGTGAC[G/T]CGGAAATAAAAGATA	23894
rs48129644	snp	C/T	0.124444	0.216185	intron-variant	Gtf2h2	Mm_Celera	13:100461385	TGCCATAACCTGAGT[C/T]GGACCCAGCACAGCT	23894
rs48131566	snp	A/G			intron-variant	Gtf2h2	GRCm38.p3	13:100486729	GAGCAGACCGACACT[A/G]AACTTGGCGAGATGT	23894
rs48227727	snp	A/G	0.132653	0.220748	intron-variant	Gtf2h2	Mm_Celera	13:100467964	AACAAAGATGTGCAG[A/G]TGAAAGCACTGACTA	23894
rs48278015	snp	A/G	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Gtf2h2	Mm_Celera	13:100468982	ATGAACAAAGACATC[A/G]CAGTCCACACAAAAA	23894
rs48374668	snp	A/C	0.132653	0.220748	upstream-variant-2KB	Gtf2h2	Mm_Celera	13:100493751	CCACCTTAATAAAAC[A/C]CTTTTCTCTGTCATT	23894
rs48424100	snp	A/G	0.132653	0.220748	downstream-variant-500B, intron-variant	Gtf2h2	Mm_Celera	13:100468148	CCTGACAGTGTAAAG[A/G]AGGAACTCCTACAGA	23894
rs48430764	snp	C/T	0.497778	0.0332592	intron-variant	Gtf2h2	GRCm38.p3	13:100481798	TTTTTCTTAGTTCTA[C/T]GTACTGCTGTGGATT	23894
rs48472378	snp	C/T	0.124444	0.216185	upstream-variant-2KB	Gtf2h2	Mm_Celera	13:100493117	AATAAGAGGATTCCC[C/T]CAATAAAATAAAAAT	23894
rs48483158	snp	A/G	0.124444	0.216185	intron-variant	Gtf2h2	Mm_Celera	13:100461729	AATCTGAACCCACAA[A/G]AACGGTTAAGGCACT	23894
rs48501402	snp	C/T			intron-variant	Gtf2h2	GRCm38.p3	13:100480487	CAAATGAAAGCAGAA[C/T]GCCTGACTTGAAGCA	23894
rs48573948	snp	G/T	0.132653	0.220748	intron-variant	Gtf2h2	Mm_Celera	13:100467324	TGAGGCCACATGACC[G/T]CAGAAAAAGGTGCAT	23894
rs48737507	snp	A/G			intron-variant	Gtf2h2	Mm_Celera	13:100471809	CTCACTCAGGATGAT[A/G]CCCTCCAGATACATC	23894

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