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
rs3708868	snp	C/T	0.48	0.0979796	intron-variant	Sh3gl3	Mm_Celera	7:82278398	GGATGCTTACCGTGT[C/T]AGAGCACTGTCTGTG	20408
rs3721231	snp	A/G	0.48	0.0979796	intron-variant	Sh3gl3	GRCm38.p3	7:82281830	CCCTTGGAAGCAGAC[A/G]CCATCTCTGCTGGTT	20408
rs6212517	snp	A/G	0.426035	0.177515	intron-variant	Sh3gl3	Mm_Celera	7:82281860	TCACATACAGCTCAC[A/G]TCCTAGGAGGCAGAG	20408
rs6212591	snp	C/T	0.32	0.24	intron-variant	Sh3gl3	Mm_Celera	7:82281902	ACTCCTGACCGTGAC[C/T]GAGATAATCCAGTTT	20408
rs6212613	snp	A/G	0.396694	0.202437	intron-variant	Sh3gl3	GRCm38.p3	7:82281919	AGATAATCCAGTTTG[A/G]ATCTGACTTGCCTTC	20408
rs6213614	snp	C/G	0.484757	0.0859605	intron-variant	Sh3gl3	GRCm38.p3	7:82282101	GAAGGATTCCAGATG[C/G]AGTTCTAGGTTGCAT	20408
rs6213682	snp	A/G	0.32	0.24	intron-variant	Sh3gl3	Mm_Celera	7:82282146	GAGAGCATAGTTGGT[A/G]TGACTCCCACTCACG	20408
rs6294891	snp	A/G	0.5	0	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82301125	GGGGAGCTGATGGAG[A/G]TTGGGGGTTGCANAT	20408
rs6294905	snp	C/T	0.5	0	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82301138	AGNTTGGGGGTTGCA[C/T]ATGTGAGGCTCCCGT	20408
rs6295397	snp	A/G	0.5	0	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82301191	AGAGCTCCATCTGAT[A/G]TCTCCTGCCCCAGTC	20408
rs6295950	snp	A/G	0.5	0	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82301283	TGGACCCTCAGTGCT[A/G]CCACACTCTGGGGAG	20408
rs6309174	snp	C/T	0.5	0	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82301367	AGCTCAGAGCACTTC[C/T]GGAGCCNCCTTGACC	20408
rs6309193	snp	A/G	0.345679	0.230967	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82301374	AGCACTTCNGGAGCC[A/G]CCTTGACCCAGAGTT	20408
rs6309268	snp	G/T	0.290657	0.246672	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82301429	ATCCTCTGGGTGTAA[G/T]CGAGGAAACCTTTCC	20408
rs6309684	snp	A/G	0.5	0	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82301460	ATGCTGTAGGCCACT[A/G]TCCCCTCTCTCCAGG	20408
rs6309711	snp	C/T	0.5	0	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82301480	CTCTCTCCAGGTCTC[C/T]CCCTGTCTAGGAAGA	20408
rs31106453	snp	A/T	0.5	0	intron-variant	Sh3gl3	GRCm38.p3	7:82277960	GATGCCAGGTCTCAG[A/T]GTAGAGCCAGCGTGG	20408
rs31140752	snp	C/T	0.359862	0.224567	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82302712	CCTGATTGTTTCACA[C/T]GCCACATGGAACACC	20408
rs31142630	snp	A/G	0.444444	0.157135	intron-variant	Sh3gl3	GRCm38.p3	7:82264888	GATGTTTGAAAGCCC[A/G]AAACTGTCATCCTCG	20408
rs31154038	snp	A/C	0.375	0.216506	downstream-variant-500B	Sh3gl3	Mm_Celera	7:82307690	AGGTTTTCAAACAGT[A/C]CCATTGTGGATGCTA	20408
rs31163289	snp	A/G	0.359862	0.224567	intron-variant	Sh3gl3	Mm_Celera	7:82285138	GACACCAGGTAAGCT[A/G]GTCATCCCGAGTGGG	20408
rs31185511	snp	C/T	0.5	0	intron-variant, splice-donor-variant	Sh3gl3, Gm36061	Mm_Celera	7:82302719	GTTTCACATGCCACA[C/T]GGAACACCGTTGTAC	20408
rs31186307	snp	A/G	0.375	0.216506	intron-variant	Sh3gl3	Mm_Celera	7:82287497	GCTGTATCCTGTTAT[A/G]TAGGTGCTAGGAACT	20408
rs31198927	snp	C/T	0.444444	0.157135	intron-variant	Sh3gl3	GRCm38.p3	7:82274730	GGCTATGTGGCGTGT[C/T]CCTGCAACAAACAGA	20408
rs31222040	snp	A/G	0.375	0.216506	downstream-variant-500B	Sh3gl3	Mm_Celera	7:82307576	TACCGATCTACACAC[A/G]GTACATCCCCTTCTC	20408
rs31249267	snp	C/T	0.32	0.24	intron-variant	Sh3gl3	Mm_Celera	7:82270193	GCCAGAACTAATAAA[C/T]ACTCAGTGCTTGAGT	20408
rs31249893	snp	A/G	0.375	0.216506	intron-variant	Sh3gl3	Mm_Celera	7:82272980	TTGTAATCTGAATTG[A/G]TTAACACAGATCCCC	20408
rs31250267	snp	A/G	0.32	0.24	intron-variant, upstream-variant-2KB	Sh3gl3, Gm36061	Mm_Celera	7:82296515	CCCGCATCCGTTCAG[A/G]TGCTGGCAGTCAGGG	20408
rs31277879	snp	C/G	0.375	0.216506	intron-variant	Sh3gl3	Mm_Celera	7:82269468	CTGTACATTTTACAA[C/G]ATGCCTGAGTTACCT	20408
rs31289295	snp	C/T	0.444444	0.157135	intron-variant	Sh3gl3	GRCm38.p3	7:82284903	GTCAGTGTGCACAGT[C/T]CTCATGCTCACTCCC	20408
rs31307419	snp	A/G	0.493827	0.0552116	intron-variant, upstream-variant-2KB	Sh3gl3, Gm36061	GRCm38.p3	7:82296688	CAGCATGAGCATTTA[A/G]TATTTCCTCTACTGA	20408
rs31323643	snp	A/C	0.5	0	intron-variant	Sh3gl3	Mm_Celera	7:82283024	AGGTCCTTCTTCAAG[A/C]CTGCAGCTCTTCTGG	20408
rs31336043	snp	C/T	0.290657	0.246672	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82298407	GCTGAATGATGTCTG[C/T]CCCAACATGTTTAGG	20408
rs31375296	snp	A/G	0.375	0.216506	intron-variant	Sh3gl3	Mm_Celera	7:82260658	CATTAGAACCGACAT[A/G]TCAGCTGTGATACAG	20408
rs31399850	snp	C/T	0.375	0.216506	intron-variant	Sh3gl3	GRCm38.p3	7:82269510	TACGTGTGAGAAGAC[C/T]GTGTCTAGAGTACAT	20408
rs31401623	snp	A/G	0.444444	0.157135	intron-variant	Sh3gl3	GRCm38.p3	7:82281052	TGGAAATTAGACTAT[A/G]GGGGGAGATGGCAGG	20408
rs31403986	snp	A/G	0.444444	0.157135	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82297363	ACAAAGCATGGACCA[A/G]GTTATACTGGAAGGG	20408
rs31425551	snp	C/T	0.5	0	intron-variant	Sh3gl3	Mm_Celera	7:82270994	ACAGAGCCCGTGCCT[C/T]TGCATTTTCATAGTT	20408
rs31434298	snp	C/T	0.35503	0.226867	intron-variant	Sh3gl3	GRCm38.p3	7:82282180	ACGATATTTGTGAAC[C/T]GCACATGCACGATCA	20408
rs31468982	snp	A/C	0.375	0.216506	intron-variant	Sh3gl3	Mm_Celera	7:82280326	TCATGTGCTTTGACT[A/C]TGAAAGGCTAGCTTG	20408
rs31472555	snp	A/C	0.375	0.216506	intron-variant, upstream-variant-2KB	Sh3gl3, Gm36061	Mm_Celera	7:82296927	TAGCTTTGGGAGTCA[A/C]AATAGAACTTGGTGG	20408
rs31494222	snp	A/T	0.375	0.216506	intron-variant	Sh3gl3	GRCm38.p3	7:82265272	TTAAAGGCGTGCGCC[A/T]CCACTGCCTGACTGG	20408
rs31506556	snp	C/G	0.444444	0.157135	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	GRCm38.p3	7:82302319	TCATCGCAGGTTGCT[C/G]ATTAAGGAAAACTAG	20408
rs31527827	snp	C/T	0.487535	0.077957	intron-variant	Sh3gl3	GRCm38.p3	7:82291832	TAAGCTCAGATGTTT[C/T]CAGGTGAGGCTTGTG	20408
rs31541120	snp	C/T	0.48	0.0979796	intron-variant	Sh3gl3	GRCm38.p3	7:82270243	CTGCCTACTACCTCC[C/T]CAGGGAAAGTTGCTG	20408
rs31545330	snp	A/G	0.444444	0.157135	intron-variant	Sh3gl3	Mm_Celera	7:82271714	TAGAGACAGGGTCTC[A/G]CCATGCACCCTTGGC	20408
rs31554422	snp	A/G	0.444444	0.157135	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82297150	TAGCATAGTTCCAGG[A/G]AACTGTATGAACACA	20408
rs31572880	snp	C/T	0.375	0.216506	intron-variant	Sh3gl3	GRCm38.p3	7:82269387	TAACGCACAGCACAG[C/T]AGGACTATCCGAGAG	20408
rs31613456	snp	A/G	0.244898	0.249948	intron-variant	Sh3gl3	Mm_Celera	7:82286844	CTGTTTCCCACTGAA[A/G]TTACAGCTGAACTGT	20408
rs31621264	snp	C/T	0.475309	0.108333	intron-variant	Sh3gl3	GRCm38.p3	7:82288487	AATCACAAGAGTACC[C/T]AGCAGACGCAACTTA	20408
rs31652992	snp	C/T	0.375	0.216506	upstream-variant-2KB	Sh3gl3	Mm_Celera	7:82259397	ACCTTTCCCGCTGTG[C/T]TGCACACTGAAATGT	20408
rs31656371	snp	C/T	0.375	0.216506	intron-variant	Sh3gl3	Mm_Celera	7:82286696	TCCTTCACTTTCCCA[C/T]GCACGCTGCCCACCC	20408
rs31676001	snp	C/G/T	0.444444	0.157135	intron-variant	Sh3gl3	GRCm38.p3	7:82274641	TCATTTGAACTTTGG[C/G/T]CTTGTCGCCATCTTT	20408
rs31691584	snp	G/T	0.444444	0.157135	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82298112	CTGAGTTAGAAATGC[G/T]CTTGAGCTGGGTGTG	20408
rs31693531	snp	A/G	0.375	0.216506	downstream-variant-500B	Sh3gl3	Mm_Celera	7:82307620	GAAAGCTTCCTGCCT[A/G]CTGGTAAGTTCACTC	20408
rs31702707	snp	G/T	0.375	0.216506	intron-variant	Sh3gl3	Mm_Celera	7:82293690	TGCCAGTGTGTGTCT[G/T]CGCCTGGTGTCACGC	20408
rs31702905	snp	A/G	0.444444	0.157135	intron-variant	Sh3gl3	Mm_Celera	7:82271826	TCTGAAAAGCCTGCA[A/G]ACAGGAGAGGGCCTT	20408
rs31733868	snp	G/T	0.48	0.0979796	intron-variant	Sh3gl3	GRCm38.p3	7:82272470	CTTCTAATTGGCAAG[G/T]AAACAGCTGTGAATT	20408
rs31771434	snp	A/G	0.5	0	intron-variant	Sh3gl3	GRCm38.p3	7:82289147	TCGTTGATAAATATG[A/G]AAATCTTTATTACCT	20408
rs31793164	snp	C/T	0.375	0.216506	intron-variant	Sh3gl3	Mm_Celera	7:82284997	GAGATCTGACTTGTC[C/T]CCCCCCACCCCCATG	20408
rs31805047	snp	C/T	0.48	0.0979796	intron-variant	Sh3gl3	Mm_Celera	7:82274409	AACTGGCAGTTTTAT[C/T]CTGGAAACCTGCAAG	20408
rs31806259	snp	C/T	0.493827	0.0552116	intron-variant, upstream-variant-2KB	Sh3gl3, Gm36061	GRCm38.p3	7:82296504	GGGACAGGAGTCCCG[C/T]ATCCGTTCAGATGCT	20408
rs31827342	snp	C/G	0.375	0.216506	intron-variant	Sh3gl3	Mm_Celera	7:82284996	AGAGATCTGACTTGT[C/G]CCCCCCCACCCCCAT	20408
rs31838704	snp	C/G	0.375	0.216506	intron-variant	Sh3gl3	GRCm38.p3	7:82269502	TATGTGGTTACGTGT[C/G]AGAAGACTGTGTCTA	20408
rs31856040	snp	G/T	0.375	0.216506	upstream-variant-2KB	Sh3gl3	GRCm38.p3	7:82259609	CATTCAGGCTGTTGG[G/T]GTGCTGCTAACTCTT	20408
rs31856236	snp	A/G	0.290657	0.246672	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82297362	TACAAAGCATGGACC[A/G]GGTTATACTGGAAGG	20408
rs31871939	snp	A/G	0.475309	0.108333	intron-variant, upstream-variant-2KB	Sh3gl3, Gm36061	GRCm38.p3	7:82296645	TGTGTCTTTGAGTAC[A/G]TGTCATCCTTAACAT	20408
rs31880334	snp	C/T	0.444444	0.157135	intron-variant	Sh3gl3	Mm_Celera	7:82278408	CGTGTCAGAGCACTG[C/T]CTGTGGCTGTGAGCA	20408
rs31888608	snp	C/T	0.497041	0.0383476	intron-variant	Sh3gl3	GRCm38.p3	7:82282831	GGGCGAAGCCTGCGA[C/T]GGGCGGTTTTGATTT	20408
rs31891396	snp	A/G	0.444444	0.157135	intron-variant	Sh3gl3	Mm_Celera	7:82278518	CCAGCACGTGTATAG[A/G]AAAAGTGTTTGCCGA	20408
rs31903222	snp	G/T	0.375	0.216506	intron-variant	Sh3gl3	GRCm38.p3	7:82270451	AAAACGGCTGCACAG[G/T]TGTCAGCATTGAGCT	20408
rs31915174	snp	A/G	0.48	0.0979796	intron-variant	Sh3gl3	Mm_Celera	7:82274117	TGAAAACTGCACTCG[A/G]TTACTATATTATATG	20408
rs31938236	snp	A/G	0.375	0.216506	intron-variant	Sh3gl3	GRCm38.p3	7:82280740	TTCTGATGCAGCATT[A/G]GTGACTGTCATAGGT	20408
rs31939581	snp	C/T	0.375	0.216506	intron-variant	Sh3gl3	GRCm38.p3	7:82294960	AGAAACTCAATTCTC[C/T]CAGGCGGTGGGGTCT	20408
rs31966787	snp	A/G	0.32	0.24	intron-variant	Sh3gl3	Mm_Celera	7:82274067	AACCAAGGTTTCTGC[A/G]TGGGCTCGGCAACCA	20408
rs31978122	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Sh3gl3, Gm36061	Mm_Celera	7:82296788	CTGAGCCCTTTGCTG[C/T]TGTCCAAGCTGAAGG	20408
rs31988129	snp	A/G	0.375	0.216506	intron-variant	Sh3gl3	Mm_Celera	7:82280254	AGAAATCCTAAGCAC[A/G]GGACTGGGCAGTCAC	20408
rs32004190	snp	C/T	0.375	0.216506	upstream-variant-2KB	Sh3gl3	Mm_Celera	7:82259464	TCTAGGAGTCAGGTC[C/T]TGAATGATCTGCCTC	20408
rs32043442	snp	C/T	0.5	0	synonymous-codon	Sh3gl3	Mm_Celera	7:82270837	GCAGGTGAAGGCCAC[C/T]GGCTACCCACAGACG	20408
rs32069559	snp	A/G	0.444444	0.157135	intron-variant	Sh3gl3	GRCm38.p3	7:82283279	TTGCTCATCCTTTCT[A/G]ATGTATGTATTTGTG	20408
rs32092673	snp	C/T	0.48	0.0979796	upstream-variant-2KB	Sh3gl3	GRCm38.p3	7:82259766	TTTTCTCATTAGTAG[C/T]TGTTGTGGTGTGCGT	20408
rs32096058	snp	A/G	0.48	0.0979796	intron-variant	Sh3gl3	Mm_Celera	7:82274075	TTTCTGCGTGGGCTC[A/G]GCAACCACACAGTCT	20408
rs32097612	snp	C/G	0.5	0	intron-variant	Sh3gl3	GRCm38.p3	7:82280342	TGAAAGGCTAGCTTG[C/G]CAACTTCAATGCCAG	20408
rs32119786	snp	C/T	0.444444	0.157135	intron-variant	Sh3gl3	GRCm38.p3	7:82270549	GTGATTTGGAGACAA[C/T]ATGGTCTGTAATGTT	20408
rs32135451	snp	C/G	0.48	0.0979796	intron-variant	Sh3gl3	GRCm38.p3	7:82270105	CTAATCCTTCCCAAA[C/G]GGTTCTGACAACTGG	20408
rs32135794	snp	C/T	0.375	0.216506	intron-variant	Sh3gl3	GRCm38.p3	7:82270440	TGTCCCTGGCAAAAA[C/T]GGCTGCACAGGTGTC	20408
rs32142061	snp	A/G	0.375	0.216506	intron-variant	Sh3gl3	Mm_Celera	7:82292412	AGGGCTGTCACACCT[A/G]TTACACACACATCCT	20408
rs32152498	snp	C/T	0.444444	0.157135	intron-variant	Sh3gl3	Mm_Celera	7:82278213	GTGCTCTGTCCTTGG[C/T]GACTTCCTGCTTATG	20408
rs32160618	snp	C/T	0.375	0.216506	intron-variant	Sh3gl3	Mm_Celera	7:82271207	ACAGGTATGCATGTG[C/T]ACAGGTATGCATGTG	20408
rs32165639	snp	A/G	0.444444	0.157135	intron-variant	Sh3gl3	GRCm38.p3	7:82264004	TCATTGCAAAAGAAA[A/G]AAAGGGGCTGTAGCC	20408
rs32165730	snp	A/C	0.444444	0.157135	intron-variant	Sh3gl3	Mm_Celera	7:82268675	AAGAAAGTCCTCTAT[A/C]CTGTTCGGAAAGATC	20408
rs32181310	snp	C/T	0.375	0.216506	upstream-variant-2KB	Sh3gl3	Mm_Celera	7:82259289	CTCTTATTGTACAGA[C/T]AGCCACAAAGGATAG	20408
rs32186227	snp	C/G	0.444444	0.157135	intron-variant	Sh3gl3	Mm_Celera	7:82274677	CCCAGACAGTTTTAA[C/G]AGTGTAGCCACCGAG	20408
rs32249767	snp	C/T	0.375	0.216506	intron-variant	Sh3gl3	Mm_Celera	7:82265258	CCCAAGTGCTGGGAT[C/T]AAAGGCGTGCGCCAC	20408
rs32266570	snp	C/T	0.304688	0.243945	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82297222	CCCTGAAGCGCTGGT[C/T]GATGGCACTTTCCTT	20408
rs32275726	snp	A/T	0.5	0	intron-variant, nc-transcript-variant	Sh3gl3, Gm36061	Mm_Celera	7:82297078	TATAGATATTAATTT[A/T]AAAAAATATTATAGA	20408
rs32291381	snp	A/G	0.48	0.0979796	intron-variant	Sh3gl3	Mm_Celera	7:82274291	ATATAACACAACGAC[A/G]TCATACTTTGGGGTG	20408
rs32309956	snp	C/T	0.5	0	intron-variant	Sh3gl3	Mm_Celera	7:82274554	TTCGGCGCTGAAGGT[C/T]CAGGCGCCCTCTTGT	20408
rs32331967	snp	A/G	0.375	0.216506	intron-variant	Sh3gl3	GRCm38.p3	7:82282191	GAACTGCACATGCAC[A/G]ATCAAGTTATTCACC	20408
rs32352835	snp	C/T	0.375	0.216506	intron-variant	Sh3gl3	Mm_Celera	7:82273071	CCTTGGTGCCAGTTT[C/T]CAGACCTGATTTTCC	20408

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