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
rs6362847	snp	A/G	0.5	0	intron-variant, downstream-variant-500B	Phf10, LOC106740, Gm34975	Mm_Celera	17:14947309	GGAGAACTATGGTAA[A/G]GGAGAGAAGTAGTCA	72057
rs6363331	snp	A/G	0.336735	0.234472	intron-variant, downstream-variant-500B	Phf10, LOC106740, Gm34975	Mm_Celera	17:14947364	GAATGTAGTCAAGTA[A/G]GAAATACACGAAGCA	72057
rs6381806	snp	C/T	0.5	0	intron-variant, nc-transcript-variant	Phf10, LOC106740, Gm34975	GRCm38.p3	17:14948488	GGGCAGCAGGAGAAG[C/T]GGGAGAGAGGCCACT	72057
rs6381841	snp	A/G	0.5	0	intron-variant, nc-transcript-variant	Phf10, LOC106740, Gm34975	Mm_Celera	17:14948517	CTGTGGCCCTTTGTA[A/G]AGATGCTACAGTTCA	72057
rs13467682	snp	A/G			downstream-variant-500B, missense, intron-variant	1600012H06Rik, Phf10, Gm34975	Mm_Celera	17:14946361	TGCTTGGATATGACC[A/G]TGGAGCTTGTTTCTA	72057
rs13467683	snp	A/C			missense	Phf10	Mm_Celera	17:14956046	AGCGACGAGATTTAT[A/C]TCACAAGGAGAAACT	72057
rs33228777	snp	A/C	0.492188	0.0620098	intron-variant, upstream-variant-2KB, nc-transcript-variant	Phf10, LOC106740, Gm34975	GRCm38.p3	17:14949232	ACTAGATGAGTGATA[A/C]TATGGATAGTTCTTC	72057
rs46537917	snp	C/T	0.152778	0.230321	utr-variant-3-prime, intron-variant	1600012H06Rik, Phf10, Gm34975	Mm_Celera	17:14945384	CCAATGCAGTGTGAA[C/T]GTTAGTGCATGGCCA	72057
rs46587921	snp	A/G/T	0.260355	0.249785	intron-variant, upstream-variant-2KB, nc-transcript-variant	Phf10, LOC106740, Gm34975	GRCm38.p3	17:14948992	CAGCTTGAAGTACCC[A/G/T]AATAGTTAGGCACAT	72057
rs47920577	snp	A/G	0.277778	0.248452	intron-variant	Phf10, Gm34975	Mm_Celera	17:14946981	TTGCCTAAATTTAGT[A/G]CTCTGTGCTCCATCA	72057
rs49125623	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14959203	ACATTTGTGGAGGCC[A/G]GAATGGACCATGAGA	72057
rs50685880	snp	A/G	0.260355	0.249785	intron-variant	Phf10, Gm34975	Mm_Celera	17:14946954	TACTCCATAAACAGC[A/G]TTAAACTTGTGTTGC	72057
rs51386858	snp	C/G	0.260355	0.249785	intron-variant, upstream-variant-2KB, nc-transcript-variant	Phf10, LOC106740, Gm34975	Mm_Celera	17:14950037	GTATACCAGCTATCT[C/G]CCAAAGGTTATACAA	72057
rs107601100	snp	C/T			utr-variant-3-prime, intron-variant	1600012H06Rik, Phf10, Gm34975	GRCm38.p3	17:14945712	CCTTTTTTTATAGAG[C/T]ACTATACGGTGTTAA	72057
rs107608485	snp	A/C			intron-variant	Phf10	GRCm38.p3	17:14956962	CAATTTTAAGATTTG[A/C]AATTCTTGGGCCGGG	72057
rs107614267	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14958600	ATAATGTTGCAAGGT[A/G]TATTGTTGGTGGAAA	72057
rs107695948	snp	A/C			intron-variant	Phf10	Mm_Celera	17:14955186	TTTAGACGCCCCCCC[A/C]AAAGAAAATAAGTAT	72057
rs107797477	snp	C/T			utr-variant-3-prime, intron-variant	1600012H06Rik, Phf10, Gm34975	GRCm38.p3	17:14945564	ACTATTCTAACAGTG[C/T]TCTCTCTCTCTCTCC	72057
rs107798515	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14953153	GAACAATGTCATCAA[A/G]TGCAACAGTTAGATA	72057
rs108106922	snp	A/G			intron-variant, nc-transcript-variant	Phf10, LOC106740, Gm34975	Mm_Celera	17:14948612	CCTCACAGACAAAGT[A/G]AAGACCAGCACTGAG	72057
rs108295388	snp	A/C			intron-variant	Phf10	Mm_Celera	17:14960513	TGGCTTGACACCGTT[A/C]ATTTTAAGCACTATT	72057
rs108518315	snp	C/T			intron-variant	Phf10	Mm_Celera	17:14958666	AGGTCCTTAAAAAGT[C/T]TGAAGACAGAATCAA	72057
rs108829103	snp	A/C			intron-variant	Phf10	Mm_Celera	17:14959767	TTCATAGTACCCTTC[A/C]GCTTACAACTGGCCC	72057
rs211901379	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14955725	GTCCCCAGTACTACA[A/G]ACGATAAAGATCTAT	72057
rs211968638	in-del	-/AAAAAACAAAAAC			intron-variant	Phf10	Mm_Celera	17:14958371	TAAGACCCTGTCTCA[-/AAAAAACAAAAAC]AAAAACAAAAACAAA	72057
rs212041130	snp	G/T			intron-variant	Phf10	Mm_Celera	17:14956356	TAGATGCTAACTCCA[G/T]TCCTGAGGTCACAGA	72057
rs212077580	snp	C/T			utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB, intron-variant	1600012H06Rik, Phf10, Wdr27, Gm34975	Mm_Celera	17:14944678	ATTGACAAACTGTTG[C/T]TGTGCTGGTGATTTA	72057
rs212521340	snp	A/C			intron-variant	Phf10	Mm_Celera	17:14957722	GGACAATAAGCAATA[A/C]TTTTATTTCTTTATA	72057
rs212663425	snp	A/T			intron-variant, upstream-variant-2KB, nc-transcript-variant	Phf10, LOC106740, Gm34975	Mm_Celera	17:14948902	TACCGTCCTACAAGT[A/T]GAGGGTAAGCACCAG	72057
rs212663549	snp	G/T			intron-variant	Phf10	Mm_Celera	17:14958559	CCTTATGTCTTTCTG[G/T]ACGCCTATCAGCAAA	72057
rs212702474	snp	A/G			intron-variant, upstream-variant-2KB, downstream-variant-500B	Phf10, LOC106740, Gm34975	Mm_Celera	17:14950751	CAAAGGTTCCTTGGA[A/G]TCAGGACCCAGTGGA	72057
rs213028764	snp	A/C			intron-variant	Phf10	Mm_Celera	17:14959211	GGAGGCCGGAATGGA[A/C]CATGAGATCCTCCAG	72057
rs213109376	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14951837	AAAGTTGGGTTCATC[A/G]TTATTTACTTCCATA	72057
rs213239528	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14952933	TTTTTCGCAATCAGA[A/G]TATTTTTCTCCCCAA	72057
rs213543405	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14959897	AACACTTTGTGATAA[A/G]CTCATAGGAGATATA	72057
rs213712050	snp	C/G			intron-variant	Phf10	Mm_Celera	17:14960762	CCACCAGGGAGGACC[C/G]GCACGTGGCGGGGGC	72057
rs214020999	snp	C/T			intron-variant	Phf10	Mm_Celera	17:14955550	ACATCTCAAAACATT[C/T]GCCAGTCTACACACG	72057
rs214236702	snp	C/T			utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB, intron-variant	1600012H06Rik, Phf10, Wdr27, Gm34975	Mm_Celera	17:14944851	ATTCAAGAAGAAATA[C/T]TTCAAATTAAGTTGC	72057
rs214250477	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14954503	AGACAAGCTCAGTGT[A/G]CTGCTCTTACCCACC	72057
rs214370360	snp	A/T			intron-variant	Phf10, Gm34975	Mm_Celera	17:14947180	TCTAAATTATTTTTT[A/T]AAAAATAGACAATAT	72057
rs214451354	in-del	-/AAAAAC			intron-variant	Phf10	Mm_Celera	17:14958372	AAGACCCTGTCTCAA[-/AAAAAC]AAAAACAAAAACAAA	72057
rs214573176	snp	C/T			intron-variant	Phf10	Mm_Celera	17:14957284	ATACATGCAAATGTA[C/T]ACATGGCAATTTCTA	72057
rs214847927	snp	A/G			missense	Phf10	GRCm38.p3	17:14961166	CACCGGCCCGGGGAc[A/G]gcgccgccccgggcc	72057
rs214900500	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14956452	GGTATGATGTTACAC[A/G]CCTATAGTCTTAGAA	72057
rs214991618	in-del	-/TTC			downstream-variant-500B, intron-variant, cds-indel	1600012H06Rik, Phf10, Gm34975	Mm_Celera	17:14945984	GAAAACACCAGCTCA[-/TTC]TATACTTCCCCCAAA	72057
rs215206818	snp	C/T			intron-variant	Phf10	Mm_Celera	17:14958623	GGTGGAAATGCAGAC[C/T]GGTACTACTGCTATG	72057
rs215245341	snp	G/T			intron-variant, upstream-variant-2KB, downstream-variant-500B	Phf10, LOC106740, Gm34975	Mm_Celera	17:14950774	CCAGTGGAGTCGCAA[G/T]TTTTTAAATGACAGA	72057
rs215377291	snp	C/G			intron-variant	Phf10	Mm_Celera	17:14960680	ACGTTCCAGGTAAGG[C/G]CCTCCCCTCCGCACC	72057
rs215609090	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14958005	ACATCACATCCAAAA[A/G]GTAGCTCAGAATGAA	72057
rs215833496	in-del	-/AA			intron-variant, upstream-variant-2KB, nc-transcript-variant	Phf10, LOC106740, Gm34975	Mm_Celera	17:14950280	GTATGCCCTGCACTC[-/AA]AAAAAAAAAAAGTTC	72057
rs215835980	in-del	-/T			intron-variant	Phf10	Mm_Celera	17:14956480	AACTTACTCTGCCCC[-/T]TTAAGAACCTGGTGA	72057
rs215882985	snp	C/T			intron-variant	Phf10	Mm_Celera	17:14951467	GTACACATGTTATCA[C/T]ACTGTGTATGCATCA	72057
rs215913449	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14960061	ACTATAAATTTCAAT[A/G]AAGGCCCACGGAAGG	72057
rs215953044	snp	C/T			intron-variant	Phf10	Mm_Celera	17:14953059	GCCACACACCCGAGG[C/T]GTGGTGACTTGTGCA	72057
rs216003016	in-del	-/T			intron-variant	Phf10	Mm_Celera	17:14960378	TAGAAATCATTCCCC[-/T]TTTCACTCTTCAAGA	72057
rs216281066	in-del	-/CACTCTC			intron-variant	Phf10	Mm_Celera	17:14953695	CCACTGCTGTCACGT[-/CACTCTC]CACTCTGCATGTGTG	72057
rs216378255	in-del	-/A			intron-variant	Phf10	Mm_Celera	17:14958450	AATAGACATTTCTCC[-/A]AAAACATAAATCAAA	72057
rs216439772	snp	A/C			intron-variant	Phf10	Mm_Celera	17:14957363	ACTTCCGGCTCTTGC[A/C]GAGGCTGAGCATTCG	72057
rs216449760	in-del	-/AAA			intron-variant	Phf10	Mm_Celera	17:14955346	TAAATGTTATCTTGT[-/AAA]AAAAAAAAAAATCAA	72057
rs216457969	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14953502	TGAGAACTGGTCTCC[A/G]GAATGAAGTCTACTG	72057
rs216476474	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14957667	AAGTCACAGACAACT[A/G]GAAAAGCAGAAATTC	72057
rs216723052	snp	C/T			intron-variant	Phf10	Mm_Celera	17:14956309	ATTAGGGCAGCTCAT[C/T]AAGAATGGCTTCCTA	72057
rs216908180	snp	G/T			utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB, intron-variant	1600012H06Rik, Phf10, Wdr27, Gm34975	Mm_Celera	17:14944666	CTGGCAGCAAGTATT[G/T]ACAAACTGTTGCTGT	72057
rs216913592	in-del	-/TC			intron-variant	Phf10	Mm_Celera	17:14960000	GCTTAAACTCCTATT[-/TC]TTTTTTTTAAATCAA	72057
rs216962942	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14958719	CTAGTTATATACCAG[A/G]GTATTAAGAACAGGG	72057
rs216997713	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14959187	TTTGCTCTCTATACA[A/G]ACATTTGTGGAGGCC	72057
rs217146900	in-del	-/AG			intron-variant	Phf10	Mm_Celera	17:14953531	TGCTGGAAGCAAAGC[-/AG]AGATTCTGAAACAAG	72057
rs217156523	snp	A/T			intron-variant	Phf10	Mm_Celera	17:14955606	CCTACTGCTGGGAAG[A/T]GCCTGTTGGCATTGA	72057
rs217342762	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14960744	TGCGAGCAGTCAGAG[A/G]CCCCACCAGGGAGGA	72057
rs217436837	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14953760	ATCCTCATTTCACAG[A/G]CGCTTCCCGAGGATA	72057
rs217448155	snp	C/G			intron-variant	Phf10	Mm_Celera	17:14954349	CCATGTGCACAGGCT[C/G]TGAAGGAAGGCAATG	72057
rs217756039	snp	G/T			intron-variant, nc-transcript-variant	Phf10, LOC106740, Gm34975	Mm_Celera	17:14948811	GGTAGCACTAACATA[G/T]TATAGATATTAATTA	72057
rs217765880	in-del	-/G			intron-variant, nc-transcript-variant	Phf10, LOC106740, Gm34975	Mm_Celera	17:14947997	GTCCTGGACATCAGT[-/G]GAAAAAAAACGCTAG	72057
rs217846668	snp	A/C			intron-variant, downstream-variant-500B	Phf10, LOC106740, Gm34975	Mm_Celera	17:14947337	TCACTATGACATGTA[A/C]TCGGACAAGGAGAAT	72057
rs217905585	snp	C/T			upstream-variant-2KB	Phf10	GRCm38.p3	17:14962270	AGCACTCAGGTTGAA[C/T]GGAACCCAGTCAGGC	72057
rs217940750	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14953866	CTCCTGACCTCACCA[A/G]CAGGCCTTCACTTCC	72057
rs217972376	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14954604	TTTCAGAAAGAAGAA[A/G]AGGAAGGAGGGTGGA	72057
rs217980960	in-del	-/GAGA			intron-variant, upstream-variant-2KB, nc-transcript-variant	Phf10, LOC106740, Gm34975	Mm_Celera	17:14949908	CCTACTTCTCAAGGG[-/GAGA]GAGAGGCAGACAGAA	72057
rs218272450	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14956569	CCTCTATAGTAGGCC[A/G]CCTCTATAGTAGGCT	72057
rs218307490	snp	C/T			intron-variant	Phf10	Mm_Celera	17:14957401	GCACCACATCAGGTA[C/T]CTCACAACTGTCCTA	72057
rs218340039	snp	A/G			intron-variant, downstream-variant-500B	Phf10, LOC106740, Gm34975	Mm_Celera	17:14947477	TACACCTAAACTACC[A/G]AGGCAAGGAAGGGAT	72057
rs218608796	snp	C/T			intron-variant	Phf10	Mm_Celera	17:14951549	GCACATGTGTGCAAA[C/T]GTGGGTAAAGTCCAT	72057
rs218627083	in-del	-/G			downstream-variant-500B, intron-variant, frameshift-variant	1600012H06Rik, Phf10, Gm34975	Mm_Celera	17:14946174	CACACAAGATAATGT[-/G]GGGTTTTGTTTTTTT	72057
rs218633416	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14952818	CCTTGAATAGTAAAT[A/G]TGTAAAAACTACTAA	72057
rs218749368	in-del	-/G			intron-variant	Phf10	Mm_Celera	17:14951263	TTATGAAAAGTGAAT[-/G]TTAAAAATTCATAGC	72057
rs219006466	snp	C/T			intron-variant, upstream-variant-2KB, nc-transcript-variant	Phf10, LOC106740, Gm34975	Mm_Celera	17:14949873	CATCCCCTTGCACCA[C/T]GACAGCTGCTCACCT	72057
rs219038388	snp	G/T			intron-variant	Phf10	Mm_Celera	17:14951010	CAGCTTCAATGTTTT[G/T]CATACCATGAGAATG	72057
rs219341804	snp	A/C			intron-variant	Phf10	Mm_Celera	17:14953209	CGACTACTTTAAGAC[A/C]CTGTACAGCATGTAC	72057
rs219370298	snp	G/T			intron-variant	Phf10	Mm_Celera	17:14953785	AGGATACCAAGCTCC[G/T]GGGCCATGTGCCACA	72057
rs221129557	in-del	-/C			intron-variant	Phf10	Mm_Celera	17:14960236	AGTGAAGTGATCACA[-/C]TAAGAGCCAGGTAGC	72057
rs221277200	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14958863	ATGAACCTTGAAGAT[A/G]CTATGGTTATGGGTA	72057
rs221550148	snp	C/T			intron-variant	Phf10	Mm_Celera	17:14960456	AAGTTGAAAGATAAT[C/T]AAATTTCTTAGTATG	72057
rs221583739	snp	G/T			intron-variant	Phf10	Mm_Celera	17:14960797	TCGGCTGGCCGGGTC[G/T]GTGGGTGTGAAACCA	72057
rs221731236	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14958257	AGCACAAAATAAAAG[A/G]GAAATGGACAGCTGG	72057
rs221775889	snp	C/T			intron-variant	Phf10	Mm_Celera	17:14956536	ACCTCTATAGTAGGC[C/T]ACCTCTATAGTAGGC	72057
rs222010114	snp	C/G			intron-variant	Phf10	Mm_Celera	17:14960318	TCATTATGTCTCCAG[C/G]ACCTAGGAATTTACT	72057
rs222349664	snp	C/G			missense	Phf10	Mm_Celera	17:14959485	ATTCGCCTCCTTTTA[C/G]ATGGATGGGTCCCAT	72057
rs222427509	in-del	-/A			intron-variant	Phf10	Mm_Celera	17:14953745	TGAGGAGAGGAGAGG[-/A]TCCTCATTTCACAGG	72057
rs222648016	snp	A/G			intron-variant	Phf10	Mm_Celera	17:14959356	GTTTCTGCTGCCTGG[A/G]ATAGGCAGGAGAAGA	72057
rs222685487	snp	C/T			intron-variant	Phf10	Mm_Celera	17:14960175	ACCAGCTGTGTGCTG[C/T]AAGCTTCTCCCCAGT	72057

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