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
rs13463820	snp	A/G			utr-variant-3-prime, nc-transcript-variant	Rnf126	Mm_Celera	10:79758637	AAGGGTGACCAGCAG[A/G]CCCAGGAACAAACTG	70294
rs211826670	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79762405	CACCCCACAGACAGG[A/G]GACAACAGTGGGACC	70294
rs211920979	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79761397	ACTAGGCCAGCCTCT[C/T]GGCCCCCCACAGATG	70294
rs212316850	snp	A/T			intron-variant	Rnf126	Mm_Celera	10:79759891	TCTGATTGTTTTAGA[A/T]GGGAGAACAAGCAGA	70294
rs212430060	snp	C/T			downstream-variant-500B	Rnf126, Fgf22	Mm_Celera	10:79758043	CACCCCAGACTATGA[C/T]AGGGTAGGAGGCAGC	70294
rs212804454	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79766036	CCCAGGCTTCCACCT[C/T]GAAGGGCAGGAGCAG	70294
rs213000510	in-del	-/TGCC			utr-variant-3-prime, nc-transcript-variant	Rnf126	Mm_Celera	10:79758867	AAGACGGACTGAAGG[-/TGCC]TGCCTGCTGGGGACA	70294
rs213216165	snp	C/T			upstream-variant-2KB	Rnf126	Mm_Celera	10:79767589	GAATCCGCCTAGGAA[C/T]TTGGCGTGAGCCTGG	70294
rs214184112	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79764120	AGCCAGCCACTACCC[A/G]TCTCGCCAGCCTATG	70294
rs214953556	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79762623	AAATGCCCAGGTCCC[C/T]CAGCCCCCAGCCCCA	70294
rs215176868	snp	A/G			synonymous-codon, nc-transcript-variant, missense	Rnf126	Mm_Celera	10:79760896	ACACACTGGGCACTC[A/G]AGCCCTGAGCCTGCA	70294
rs215227439	snp	C/T			upstream-variant-2KB	Rnf126	Mm_Celera	10:79767724	AGTTTCTCCGGCATA[C/T]GGGATTGGATGTAGA	70294
rs215341047	snp	C/G			intron-variant	Rnf126	Mm_Celera	10:79766309	AGGGTCCTCAGGATA[C/G]ATATGTCCAAAGCTA	70294
rs215601744	snp	A/T			intron-variant	Rnf126	Mm_Celera	10:79761244	GTGCAGCTCTGGTAC[A/T]GGCCACTGTGCACCC	70294
rs215648628	snp	G/T			intron-variant	Rnf126	Mm_Celera	10:79760074	CAAAGACTGAAGGAA[G/T]GACCATCCAGAGACT	70294
rs215696800	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79760251	TATCCACTGGACAGA[A/G]CACAGGGTCCCCAAT	70294
rs216543281	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79765680	AGGTTCACCTGGCAC[C/T]CCACATACCACTCTC	70294
rs216651033	snp	A/C			intron-variant	Rnf126	Mm_Celera	10:79764320	CCCTGGACCCATGAG[A/C]AGGTAAAACAAGGAG	70294
rs219536351	snp	C/T			upstream-variant-2KB	Rnf126	Mm_Celera	10:79767924	ATTTCCCAGCTTCCT[C/T]CCCCTCATTTAGCCT	70294
rs220052741	snp	C/T			utr-variant-3-prime, nc-transcript-variant	Rnf126	Mm_Celera	10:79759020	TGGCGGGCGGGCAGG[C/T]GGGCGGTGCTGGGGC	70294
rs220173850	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79760370	CTCCCTGAGACTAAG[C/T]CATCAAAGAAAACAT	70294
rs220684724	snp	C/G			upstream-variant-2KB	Rnf126	Mm_Celera	10:79768468	GAGGGTACATTGCAA[C/G]CAGAGTTTTGAAGAA	70294
rs220955897	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79764864	CCAAGGTTGTGCTCG[A/G]GCTACAGCTGACAAT	70294
rs220966230	snp	C/G			intron-variant	Rnf126	Mm_Celera	10:79763686	GCAGCTAATGCCAAG[C/G]GTCACCATGCCCTGC	70294
rs221145665	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79764668	AGTAAGATATATTTA[C/T]ATTACAATTTATAAC	70294
rs221311982	snp	C/T			downstream-variant-500B	Rnf126	Mm_Celera	10:79758267	CGTATGTAGGCCTGC[C/T]GTCATACATGCTGCA	70294
rs221467378	in-del	-/GCAGAGGCTTCAAA			upstream-variant-2KB	Rnf126	Mm_Celera	10:79768660	GTCTACTGTGGTGAG[-/GCAGAGGCTTCAAA]GCAGCCCCTCAGTCG	70294
rs221776323	snp	A/C			intron-variant	Rnf126	Mm_Celera	10:79763309	AGCCCACTCGGCACT[A/C]TGACACGTGAAGCCT	70294
rs222236958	snp	C/T			downstream-variant-500B	Rnf126	Mm_Celera	10:79758162	GAAAGCAGTGACCAC[C/T]TTAGGCCGTAGGGGT	70294
rs222279207	in-del	-/TACT			intron-variant	Rnf126	Mm_Celera	10:79763966	ACCTCTGCTCTGCCC[-/TACT]CTACTCTGTACAGGA	70294
rs222596976	snp	C/G			upstream-variant-2KB	Rnf126	Mm_Celera	10:79768110	TAAAAACAGTGCCGG[C/G]CAGAAGGGAGTATCA	70294
rs222696768	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79762930	CAATGGTAGGACGTG[A/G]ACAGCTAGGGACCCA	70294
rs222710171	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79761826	ACTATTTCACAGGGA[C/T]TCCTGGTAGGCAGAG	70294
rs222939295	snp	C/T			upstream-variant-2KB	Rnf126	GRCm38.p3	10:79767056	CGGAAGCCAGAGACC[C/T]GGGTCCAGTGTGTGG	70294
rs222967402	snp	C/T			upstream-variant-2KB	Rnf126	Mm_Celera	10:79767245	GAAGAGTGCGGAAGT[C/T]CAGGGACAGCGCGAA	70294
rs223009237	snp	G/T			intron-variant	Rnf126	Mm_Celera	10:79764980	GGTGTCTCTGGCGGT[G/T]AACTCAGGTGTCTGA	70294
rs223167420	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79760517	CCAGGGCCAGGAAGC[A/G]GGAGTGGGTGGGTTG	70294
rs223170907	in-del	-/CTCTTCTT			upstream-variant-2KB	Rnf126	Mm_Celera	10:79767883	CCTAAGAGACTCCTC[-/CTCTTCTT]CTCTTCTTCGAACCA	70294
rs223341358	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79761705	TGCAGCCCACACTGG[C/T]CTCCAATGCAGTAAC	70294
rs223659066	in-del	-/A			upstream-variant-2KB	Rnf126	Mm_Celera	10:79767834	GTTAGGGCTATCCCT[-/A]AAAAAAAAAAAAAAA	70294
rs223662988	in-del	-/GCC			cds-indel	Rnf126	Mm_Celera	10:79758968	GGCCCGCCAGGTACT[-/GCC]GGCCGCCACGGGCAG	70294
rs226485007	snp	A/T			upstream-variant-2KB	Rnf126	Mm_Celera	10:79768683	CTCAGTCGTTTAAAC[A/T]CGCCAATATTCAATG	70294
rs227064289	snp	A/G			upstream-variant-2KB	Rnf126	Mm_Celera	10:79767313	CAGACATGGAAGCAG[A/G]AGAAGTCAGAGATGG	70294
rs227105560	snp	A/G			synonymous-codon, nc-transcript-variant	Rnf126	GRCm38.p3	10:79762162	GGGCTGCCGGGCCCC[A/G]TACCGATGCCGAGAC	70294
rs227159754	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79765160	ACACGCCTTTAATCT[C/T]AGTACTTGAGAGGCA	70294
rs227190346	in-del	-/GGCGGGCG			utr-variant-3-prime, nc-transcript-variant	Rnf126	Mm_Celera	10:79759006	CTAGTCCACAGCCAT[-/GGCGGGCG]GGCAGGCGGGCGGTG	70294
rs227211774	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79760956	ACACGGGGAGGTCCC[C/T]GGGGACTCTGTCCAC	70294
rs227950538	snp	G/T			intron-variant	Rnf126	Mm_Celera	10:79762385	GCAGAGGCAGAGTCC[G/T]TGACCACCCCACAGA	70294
rs227983908	in-del	-/GAAG			upstream-variant-2KB	Rnf126	Mm_Celera	10:79767360	GGGCTACGTGGGGGA[-/GAAG]GAAGACTTTTTGGCA	70294
rs228329255	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79763941	CTGGCCACAGCGTTA[C/T]TGTCTGCAGACCTCT	70294
rs228529944	in-del	-/A			intron-variant	Rnf126	Mm_Celera	10:79760350	CTAACCAGTATCCCC[-/A]AGAGCTCCCTGAGAC	70294
rs228599571	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79760723	CTTGGCATGCAAGCA[A/G]GACGGATGTCTGGGC	70294
rs228699421	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79759685	CCTTTAGTCCCAGCA[C/T]TTGGGAGGCAGAGGC	70294
rs228797497	snp	A/C			intron-variant	Rnf126	Mm_Celera	10:79765080	ACCCACAGACCTGCC[A/C]CTGCTCCCTGTCCCA	70294
rs229087712	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79760733	AAGCAGGACGGATGT[C/T]TGGGCCTGCGCTGGA	70294
rs229498631	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79762023	AGTGGAGTGTGCTTG[C/T]CTCCCATGTCTGTGT	70294
rs229594681	snp	G/T			intron-variant	Rnf126	Mm_Celera	10:79759956	GCTCACCACCATCTG[G/T]ACAGCTACAGTGTAC	70294
rs229595521	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79763821	CTGTAGGATATCACA[A/G]GACATAGGGTCCCCT	70294
rs229950661	snp	G/T			upstream-variant-2KB	Rnf126	Mm_Celera	10:79767595	GCCTAGGAATTTGGC[G/T]TGAGCCTGGAGGCGG	70294
rs230080371	snp	A/T			upstream-variant-2KB	Rnf126	Mm_Celera	10:79768779	TTCCCAATCAAGCCA[A/T]TGCTGTGTCATTGGG	70294
rs230927844	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79759652	AGAGTTTCTGATTGC[A/G]GGCAATGGTGGCGTA	70294
rs231588366	in-del	-/ACACACACACACACACACACACAC			upstream-variant-2KB	Rnf126	Mm_Celera	10:79768855	TGGGAGCCTTCTCAT[-/ACACACACACACACACACACACAC]ACACACACACACACA	70294
rs232190720	in-del	-/G			intron-variant	Rnf126	Mm_Celera	10:79760945	GAGGCATGCCAACAC[-/G]GGGAGGTCCCCGGGG	70294
rs233649947	snp	C/G			upstream-variant-2KB	Rnf126	Mm_Celera	10:79767805	GACTTGGTTGCCTTG[C/G]CAATGGCTTAAGTTG	70294
rs233705678	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79766399	AAAGCCACACTGAAG[C/T]CTTAGCACAAGGCCT	70294
rs233756744	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79765853	CGCCCTGAAGAATGT[C/T]ATGGTGTCACCATCC	70294
rs233757448	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79764124	AGCCACTACCCGTCT[C/T]GCCAGCCTATGTATC	70294
rs233773270	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79762626	TGCCCAGGTCCCTCA[A/G]CCCCCAGCCCCAGGC	70294
rs234005511	snp	G/T			intron-variant	Rnf126	Mm_Celera	10:79761263	CACTGTGCACCCTAG[G/T]ACAGCAGGCATTCTT	70294
rs234107205	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79760311	TGAAGGGGTTTGCAG[C/T]CCATAGGAGGACAAT	70294
rs234782448	snp	C/G			upstream-variant-2KB	Rnf126	Mm_Celera	10:79767469	GGCAACCTGGGGTAG[C/G]TTATAACCTGTAGGC	70294
rs235345935	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79761675	TGCAGACCACCTCAC[A/G]AGATAGGCTTGCTCT	70294
rs235824423	snp	A/G			downstream-variant-500B	Rnf126, Fgf22	Mm_Celera	10:79758070	CAGCGATCCCAGCAC[A/G]GGGCTGAAGTAAGAT	70294
rs236284368	snp	G/T			intron-variant	Rnf126	Mm_Celera	10:79764688	CAATTTATAACAGTA[G/T]CGTAATTATAGATAC	70294
rs236447228	snp	A/T			intron-variant	Rnf126	Mm_Celera	10:79762945	GACAGCTAGGGACCC[A/T]TGTAGGGACAGCAAG	70294
rs236581230	snp	A/G			upstream-variant-2KB	Rnf126	Mm_Celera	10:79768080	TACATACACTTATGT[A/G]CACCTGATAATCTGT	70294
rs236658689	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79760113	TGGGGATCCACCCCA[C/T]AAACCACCAACCCCA	70294
rs236771606	in-del	-/A			intron-variant	Rnf126	Mm_Celera	10:79761654	AAGAGACAGTGTCAC[-/A]GGGCCTGCAGACCAC	70294
rs237016617	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79762435	CAGTAAGAAGCCACC[A/G]ACCTGCAGGCTGGGA	70294
rs238158505	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79766118	CACCTTTCCAGGAGC[A/G]AGCCTCAAACCTGGG	70294
rs238706952	snp	C/T			downstream-variant-500B	Rnf126	Mm_Celera	10:79758169	GTGACCACTTTAGGC[C/T]GTAGGGGTGTTCTGG	70294
rs239891316	in-del	-/G			upstream-variant-2KB	Rnf126	Mm_Celera	10:79767390	AACCTGCGTGGGACA[-/G]GGCCTCGGGGAAGCC	70294
rs240066736	snp	C/T			upstream-variant-2KB	Rnf126	Mm_Celera	10:79768151	ATACACATCAGGTGT[C/T]CCACAAACACCCGAG	70294
rs240299234	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79764880	GCTACAGCTGACAAT[C/T]GACCCTGTGCTGAGA	70294
rs240311817	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79763720	ACTCTGGTTACTCTG[C/T]TCCTGAGAGCAGCTG	70294
rs240476437	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79761712	CACACTGGCCTCCAA[C/T]GCAGTAACCAGACCA	70294
rs240583313	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79760681	TAAGGTGGGAGTTGT[A/G]TCTGTCAGGCTTAGG	70294
rs240705790	snp	C/T			downstream-variant-500B	Rnf126	Mm_Celera	10:79758276	GCCTGCCGTCATACA[C/T]GCTGCAAGTCCATCA	70294
rs240987921	snp	C/T			upstream-variant-2KB	Rnf126	Mm_Celera	10:79768566	CCTGCTTTCTGTCCC[C/T]ATTCCCACCCATTCC	70294
rs241048655	snp	C/T			upstream-variant-2KB	Rnf126	Mm_Celera	10:79767421	TCCGCGACCAAAGGG[C/T]GGGGCCTTCGTGGGG	70294
rs241149247	in-del	-/CCAC			intron-variant	Rnf126	Mm_Celera	10:79762359	AGTGAGCCTGCCGCT[-/CCAC]CCCACAGACAGCAGA	70294
rs241546502	snp	C/T			upstream-variant-2KB	Rnf126	GRCm38.p3	10:79767080	TGTGTGGGGCGGAGC[C/T]TGGGGGCGAAGCGGC	70294
rs242106044	in-del	-/A			intron-variant	Rnf126	Mm_Celera	10:79764201	GGGGACCCTGTCTGT[-/A]GGAGTGTCTCTGCCC	70294
rs242126033	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79759413	GGGCAGTCTGGGTCC[A/G]GGTTGAGGATCCAAG	70294
rs242799578	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79765142	CGGTCAGGTGGTGGC[A/G]GAACACGCCTTTAAT	70294
rs242842021	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79761849	AGGCAGAGGCCATGG[A/G]GCATGCATGACCCAA	70294
rs242901952	snp	C/T			intron-variant	Rnf126	Mm_Celera	10:79760730	TGCAAGCAGGACGGA[C/T]GTCTGGGCCTGCGCT	70294
rs243055838	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79764339	TAAAACAAGGAGGCA[A/G]GCTGCAGGTGCCTGC	70294
rs243447365	snp	A/G			intron-variant	Rnf126	Mm_Celera	10:79762053	TGTCCCAGTGGTAGC[A/G]AAGCCCTCACCAGCT	70294
rs243828371	snp	A/T			upstream-variant-2KB	Rnf126	Mm_Celera	10:79768734	GCTCAGGGTAGTTGA[A/T]AAGTTATGGGGCAGT	70294

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