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
rs6200236	snp	C/G	0.46281	0.131194	intron-variant	Llgl2	GRCm38.p3	11:115847383	TGGTCTCGGGTGTGG[C/G]CTGCCTCACTCACAG	217325
rs6214169	snp	A/G	0.5	0	intron-variant	Llgl2	GRCm38.p3	11:115847679	CCTCGCGCTTTGTAT[A/G]GACAGCCTTCCTGGC	217325
rs6214642	snp	A/G	0.5	0	intron-variant	Llgl2	GRCm38.p3	11:115847792	TTGTTAGATCTCTCA[A/G]TAGACGGTCTCTGCA	217325
rs6214685	snp	C/T	0.5	0	intron-variant	Llgl2	GRCm38.p3	11:115847820	GCAAAAGCCCCTCCT[C/T]CCATCCCTTCCTTCA	217325
rs6215142	snp	A/T	0.5	0	intron-variant	Llgl2	GRCm38.p3	11:115847874	GCTGGAGTTCCTGAC[A/T]CTTGTGGCCCNGTGT	217325
rs6215167	snp	A/G	0.5	0	intron-variant	Llgl2	GRCm38.p3	11:115847885	TGACNCTTGTGGCCC[A/G]GTGTGGGGACAGTTT	217325
rs6287775	snp	A/G	0.5	0	intron-variant	Llgl2	Mm_Celera	11:115852095	GAGAGCCCGCCCTTA[A/G]ACCTAGCCCAACTTC	217325
rs6288219	snp	C/T	0.5	0	missense, nc-transcript-variant	Llgl2	Mm_Celera	11:115852139	CCCAGGCTGTGAATA[C/T]CAAGNCTGAGCGGAC	217325
rs6288223	snp	A/G	0.5	0	missense, nc-transcript-variant	Llgl2	Mm_Celera	11:115852144	GCTGTGAATANCAAG[A/G]CTGAGCGGACGGGCC	217325
rs6288315	snp	C/T	0.493827	0.0552116	synonymous-codon, nc-transcript-variant	Llgl2	GRCm38.p3	11:115852203	ACGGAAGATTGAGGC[C/T]CGCTCCGCGGAGGAC	217325
rs6288881	snp	C/T	0.304688	0.243945	intron-variant	Llgl2	Mm_Celera	11:115852334	GGGAGACACTCATGG[C/T]GTGAGGCCACGGAGA	217325
rs6289322	snp	A/G	0.290657	0.246672	intron-variant	Llgl2	Mm_Celera	11:115852379	CATGAGGAAGTGGGC[A/G]GATGGGTACTTCCGG	217325
rs6289422	snp	A/G	0.359862	0.224567	intron-variant	Llgl2	Mm_Celera	11:115852425	GCAGAGCTGCTGCCC[A/G]GGACCCTCAGAGCGG	217325
rs13467394	snp	A/G	0.444444	0.157135	synonymous-codon, nc-transcript-variant	Llgl2	GRCm38.p3	11:115850276	CGATGATCCGCGGCT[A/G]GGCATCCAGAAGATT	217325
rs13467395	snp	C/T	0.48	0.0979796	synonymous-codon, nc-transcript-variant	Llgl2	GRCm38.p3	11:115844864	TCTGCTGGATGACAA[C/T]AGCCTGCACCTGTGG	217325
rs13467396	snp	G/T	0.444444	0.157135	missense, nc-transcript-variant	Llgl2	GRCm38.p3	11:115850112	CCAGCGAGAACCTCA[G/T]TGCCCAGGGTGAGGA	217325
rs13467397	snp	A/G			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	Llgl2	GRCm38.p3	11:115855538	GCCAGCCCAAGCCGG[A/G]CCAGGGGCTGCCAGT	217325
rs27001640	snp	C/G	0.345679	0.230967	downstream-variant-500B	Llgl2	Mm_Celera	11:115855994	CTCCTAAGGTCCCAG[C/G]AACAAACTGAGACCT	217325
rs27001641	snp	A/G	0.5	0	downstream-variant-500B	Llgl2	Mm_Celera	11:115855923	TTTGAATCACCAAGC[A/G]TTGCTAACTTTCCAG	217325
rs27001642	snp	G/T	0.489796	0.070696	downstream-variant-500B	Llgl2	Mm_Celera	11:115855804	GGACCCGTGCTTCTC[G/T]GTGCTTCTGGTCCAT	217325
rs27001643	snp	A/G	0.124444	0.216185	downstream-variant-500B	Llgl2	Mm_Celera	11:115855783	GTCTTCACTTTAACA[A/G]CCTGAGGACCCGTGC	217325
rs27001644	snp	C/T	0.497778	0.0332592	intron-variant, downstream-variant-500B	Llgl2	GRCm38.p3	11:115855463	GTCTGTGTCCTTCCA[C/T]AGCAGAATGACTGGG	217325
rs27001645	snp	C/T	0.132653	0.220748	missense, nc-transcript-variant, downstream-variant-500B	Llgl2	Mm_Celera	11:115855224	ATCCTCACCGCGTGG[C/T]TGTGGGTTGCAGGCT	217325
rs27001646	snp	C/G	0.124444	0.216185	missense, nc-transcript-variant, downstream-variant-500B	Llgl2	Mm_Celera	11:115855220	TGGCATCCTCACCGC[C/G]TGGCTGTGGGTTGCA	217325
rs27001647	snp	A/G	0.497778	0.0332592	intron-variant, nc-transcript-variant	Llgl2	GRCm38.p3	11:115854689	CAAGATAGTCTGGGA[A/G]CAGGAGTGGACAGTT	217325
rs27001648	snp	A/G	0.48	0.0979796	intron-variant	Llgl2	GRCm38.p3	11:115854477	CCAATCAAACAGGTC[A/G]ACCTCACCCATTCCT	217325
rs27001649	snp	A/G	0.489796	0.070696	intron-variant	Llgl2	GRCm38.p3	11:115854427	ACTCCTTCCCTTGCC[A/G]CTGCCAGTCCAGACC	217325
rs27001650	snp	C/T	0.497778	0.0332592	intron-variant	Llgl2	GRCm38.p3	11:115854382	GGCCCAGAGGCTCCT[C/T]CTGAGGCATCTGCTA	217325
rs27001651	snp	C/T	0.277778	0.248452	intron-variant	Llgl2	Mm_Celera	11:115854369	AGGTGAGGACGAAGG[C/T]CCAGAGGCTCCTCCT	217325
rs27001652	snp	A/G	0.391111	0.206368	synonymous-codon, nc-transcript-variant	Llgl2	GRCm38.p3	11:115854257	CAAGTGGCTGGTTGA[A/G]CCCCGGTGTTTGGTG	217325
rs27001653	snp	C/T	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115854221	ATCACCTTCGGAGTT[C/T]GAGCGCTTTTCTCTC	217325
rs27001654	snp	C/T	0.124444	0.216185	intron-variant	Llgl2	Mm_Celera	11:115854182	CTCAGGGCTCTTCTG[C/T]CTCTCCCCAGGTTTC	217325
rs27001655	snp	A/G	0.391111	0.206368	intron-variant	Llgl2	GRCm38.p3	11:115853698	GTGCGACTCATGTCC[A/G]ACTACCATGTGTGCC	217325
rs27001656	snp	A/G	0.231111	0.249285	intron-variant	Llgl2	Mm_Celera	11:115853687	AGTCTGGTTATGTGC[A/G]ACTCATGTCCAACTA	217325
rs27001657	snp	C/T	0.48	0.0979796	intron-variant	Llgl2	GRCm38.p3	11:115853671	TGGGTGGGAAGACCA[C/T]AGTCTGGTTATGTGC	217325
rs27001658	snp	A/G	0.48	0.0979796	intron-variant	Llgl2	GRCm38.p3	11:115853604	CCAAAGGTCAGAGCT[A/G]GGAATACCAAGGCTG	217325
rs27001659	snp	A/G	0.497041	0.0383476	intron-variant	Llgl2	GRCm38.p3	11:115853544	AGTAAGGGCCACAGG[A/G]TCACAGAAAATAAGG	217325
rs27001660	snp	A/G	0.124444	0.216185	intron-variant	Llgl2	Mm_Celera	11:115853519	ACAAGGACAGCTGGG[A/G]TTGCATTGGAGTAAG	217325
rs27001661	snp	C/T	0.48	0.0979796	intron-variant	Llgl2	GRCm38.p3	11:115853499	CAGCCCCTGGGTGGA[C/T]ACAAACAAGGACAGC	217325
rs27001662	snp	C/T	0.132653	0.220748	intron-variant	Llgl2	Mm_Celera	11:115853441	CAATTCAAGGTGCCA[C/T]GTGACAGGGTCCCCT	217325
rs27001663	snp	C/T	0.497778	0.0332592	intron-variant	Llgl2	GRCm38.p3	11:115853213	GTGGTGTCACCAAGC[C/T]ACCCATCATAGCCCT	217325
rs27001664	snp	C/T	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115853093	GTCTACGCCTTTTCC[C/T]TGCGCGTGCCTCCTG	217325
rs27001665	snp	C/T	0.391111	0.206368	synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115853032	TACTGTTTTGGCAGG[C/T]TCCCGCCACTGTCCC	217325
rs27001666	snp	A/G	0.497778	0.0332592	intron-variant	Llgl2	GRCm38.p3	11:115852956	GTAGCAAGGCTGGGT[A/G]GAAGCCCGGGTTGCT	217325
rs27001667	snp	C/T	0.426035	0.177515	intron-variant	Llgl2	GRCm38.p3	11:115852778	AGGGAACTGAATCTT[C/T]AAAAAGCTTGCCAGC	217325
rs27015768	snp	A/G	0.391111	0.206368	intron-variant	Llgl2	GRCm38.p3	11:115852655	GCTGTGTCCCTGCAA[A/G]GGCAGAGCTGTCCTC	217325
rs27015769	snp	A/G	0.489796	0.070696	intron-variant	Llgl2	GRCm38.p3	11:115852365	GATGGGCTCTCTGCC[A/G]TGAGGAAGTGGGCGG	217325
rs27015770	snp	A/G	0.124444	0.216185	intron-variant	Llgl2	Mm_Celera	11:115852316	GTAGGACACATCCCT[A/G]GTGGGAGACACTCAT	217325
rs27015771	snp	A/G	0.375	0.216506	missense, nc-transcript-variant	Llgl2	Mm_Celera	11:115852210	ATTGAGGCTCGCTCC[A/G]CGGAGGACTCCTTCA	217325
rs27015772	snp	A/G	0.197531	0.244432	synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115852119	CAACTTCCTGCAGGC[A/G]CAGGCCCAGGCTGTG	217325
rs27015773	snp	A/G	0.391111	0.206368	intron-variant	Llgl2	GRCm38.p3	11:115852002	GAATCTCTTACTTGC[A/G]CAAAAGTCCTCTTGG	217325
rs27015774	snp	A/G	0.124444	0.216185	intron-variant	Llgl2	Mm_Celera	11:115851951	TGTTCCTTTCCCTCC[A/G]TGAAATGCTCGAAGG	217325
rs27015775	snp	C/G	0.426035	0.177515	intron-variant	Llgl2	GRCm38.p3	11:115851521	TAACCCATGGAATTC[C/G]AGAAAGTCTGGTGTT	217325
rs27015776	snp	C/T	0.124444	0.216185	intron-variant	Llgl2	Mm_Celera	11:115851338	TACTTATGTTAGAGT[C/T]AAGTCCCGAGCAAAT	217325
rs27015777	snp	C/T	0.48	0.0979796	synonymous-codon, nc-transcript-variant	Llgl2	GRCm38.p3	11:115851107	ATTCCGTCGGATGCG[C/T]CGCAGCAGAGTGTCC	217325
rs27015778	snp	C/T	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115851056	GGAGGGCCCTCTGTC[C/T]CGAGTAAAGTCCCTC	217325
rs27015779	snp	A/G	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115850583	AGTCCTTTGCTGACC[A/G]GGCTGTCTAGCCTCT	217325
rs27015780	snp	C/T	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115850498	CCCCAGAGTGATGAC[C/T]GTTCCGCCTCCAGAA	217325
rs27015781	snp	A/G	0.444444	0.157135	synonymous-codon, nc-transcript-variant	Llgl2	GRCm38.p3	11:115849565	CGAGGAGGAACTGGT[A/G]GTCATTGACCTGCAG	217325
rs27015782	snp	A/G	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115849372	CGCGAGGCCTTGGTC[A/G]TGGCACTTCAGCTTA	217325
rs27015783	snp	A/G	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115848765	ACAAGACAAGGGTTG[A/G]CATAGACCCTGGGAG	217325
rs27015784	snp	A/G	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115848737	CCAGCAAGGGTTGGC[A/G]TACAGAAAACAGACA	217325
rs27015785	snp	A/G	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115848613	ATGCCAGTCCAGCTT[A/G]GCGAGAGGGTCCTGG	217325
rs27015786	snp	C/T	0.48	0.0979796	intron-variant	Llgl2	Mm_Celera	11:115848605	CTGGATTTATGCCAG[C/T]CCAGCTTAGCGAGAG	217325
rs27015787	snp	C/G	0.493827	0.0552116	intron-variant	Llgl2	GRCm38.p3	11:115847582	TCAAGGTGACACTTT[C/G]TTTTAGGTCCCTTTC	217325
rs27015788	snp	C/T	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115846916	CATGGCACTCCCTTG[C/T]CTAGGTTGCCAGAGG	217325
rs27015789	snp	A/G	0.48	0.0979796	intron-variant	Llgl2	GRCm38.p3	11:115845096	CATCTCGTGCTCTGG[A/G]ACTCCTTTAAGACAG	217325
rs27015790	snp	C/T	0.48	0.0979796	intron-variant	Llgl2	GRCm38.p3	11:115845039	ATCTCTTGGGTCCTG[C/T]TGAACCCTTGGCAGT	217325
rs27015791	snp	C/G	0.495868	0.0452663	intron-variant	Llgl2	GRCm38.p3	11:115844785	GCCCTGAAGAACTAA[C/G]GCTGCTCTCTGTAGC	217325
rs27015792	snp	A/G	0.473373	0.11227	intron-variant	Llgl2	GRCm38.p3	11:115842662	GCTCCTTGCACACCA[A/G]CGGTGAAAAAGGCCC	217325
rs27015793	snp	C/T	0.142012	0.225474	intron-variant	Llgl2	Mm_Celera	11:115842619	ATGCTTTGACATCAG[C/T]TGTTGGCATTCGCAC	217325
rs27015794	snp	G/T	0.142012	0.225474	intron-variant	Llgl2	Mm_Celera	11:115841805	TGATACAAGTGAGCC[G/T]TGGCCGCTTGACTGC	217325
rs27015795	snp	A/G	0.142012	0.225474	intron-variant	Llgl2	Mm_Celera	11:115840483	TGGCCTCAGAGGCCA[A/G]AAATCTGAAAATGTG	217325
rs27015796	snp	G/T	0.492188	0.0620098	intron-variant	Llgl2	GRCm38.p3	11:115839795	ACAAGAGTCTTAGCT[G/T]CTGTGGAAGGGACAC	217325
rs27015797	snp	A/G	0.142012	0.225474	intron-variant	Llgl2	Mm_Celera	11:115839244	CCCCTGACAGACACT[A/G]CAGGGTCCCCAAAGC	217325
rs27015798	snp	A/G	0.142012	0.225474	intron-variant	Llgl2	GRCm38.p3	11:115838918	AGGTGCCTGCGCTGG[A/G]CTGCTGCAGAATAAC	217325
rs27015799	snp	C/T	0.142012	0.225474	intron-variant	Llgl2	Mm_Celera	11:115838832	GAACATTGTTTGGGG[C/T]CTGCTTGCCCCTCTG	217325
rs27015800	snp	A/G	0.142012	0.225474	intron-variant	Llgl2	Mm_Celera	11:115838690	CTGTCTACCACTTGT[A/G]CCCTCTTAGCACACT	217325
rs27015801	snp	A/G	0.142012	0.225474	intron-variant	Llgl2	Mm_Celera	11:115838636	CTTATGGGCAGCATC[A/G]AGTAGCATGGTTTGC	217325
rs27015802	snp	A/C	0.142012	0.225474	intron-variant	Llgl2	Mm_Celera	11:115837994	TCGCCCGCCACACGA[A/C]AGATGCCCAAACAGC	217325
rs27015803	snp	A/T	0.142012	0.225474	intron-variant	Llgl2	Mm_Celera	11:115837785	GTGTCCACCGAGTGC[A/T]TGGCTAAACGCCACA	217325
rs27015804	snp	A/G	0.231111	0.249285	intron-variant	Llgl2	Mm_Celera	11:115837580	GTGCCCGGTCACTCT[A/G]ACCATTTTGATGAGA	217325
rs27015805	snp	C/T	0.336735	0.234472	intron-variant	Llgl2	Mm_Celera	11:115836708	TACTCCACCTTAACC[C/T]CTGATCCGTACAGTC	217325
rs27015806	snp	G/T	0.244898	0.249948	intron-variant	Llgl2	Mm_Celera	11:115836366	AGGGAATCGGTCACG[G/T]GTGCTGGGTGGAACC	217325
rs27015807	snp	A/G	0.231111	0.249285	intron-variant	Llgl2	Mm_Celera	11:115836175	CAGAAGTTTGATGTA[A/G]GGTGCCCAGCTCACC	217325
rs27015808	snp	G/T	0.231111	0.249285	intron-variant	Llgl2	Mm_Celera	11:115836156	CACCTCCTAGAGCCG[G/T]GTCCAGAAGTTTGAT	217325
rs27015809	snp	A/G	0.231111	0.249285	intron-variant	Llgl2	Mm_Celera	11:115835800	GAGGATTGAGCCCAA[A/G]CCATCTCAGTAACCA	217325
rs27015810	snp	A/G	0.231111	0.249285	intron-variant	Llgl2	Mm_Celera	11:115835682	TCTGCTTTGATCTAT[A/G]TCCGAAGTAGATTGT	217325
rs27015811	snp	C/T	0.124444	0.216185	intron-variant	Llgl2	Mm_Celera	11:115835567	AAGGAAGCTGGGCCT[C/T]GGAAGGCTAAAGAGT	217325
rs27015812	snp	C/T	0.244898	0.249948	intron-variant	Llgl2	Mm_Celera	11:115834430	CTCCAGGAACCAAGG[C/T]CTCACTGTCTCCCTG	217325
rs27015813	snp	C/T	0.475309	0.108333	intron-variant	Llgl2	GRCm38.p3	11:115833475	CAGCGTTCAGCGAGC[C/T]GGCGGCTATGTTTGC	217325
rs27015814	snp	A/G	0.484429	0.0868505	intron-variant	Llgl2	GRCm38.p3	11:115833455	TGTCTACCTGACCCT[A/G]CATGCAGCGTTCAGC	217325
rs27015815	snp	A/G	0.231111	0.249285	intron-variant	Llgl2	Mm_Celera	11:115833193	AACTGGGGAGCCCCA[A/G]TCTTAAATCCAGAGT	217325
rs27015816	snp	A/G	0.5	0	intron-variant, nc-transcript-variant	Llgl2	GRCm38.p3	11:115832840	TGGCCGAAGTCTGGG[A/G]CCTGTTTTCACTCCA	217325
rs27015817	snp	G/T	0.429688	0.173817	intron-variant	Llgl2	Mm_Celera	11:115832644	CCCTAGAGTCCGCTG[G/T]TCTCTTTCCTTTCCC	217325
rs27015818	snp	A/G	0.124444	0.216185	intron-variant	Llgl2	Mm_Celera	11:115832451	AGGGGGTCTGGAACA[A/G]TGCTGGTCACAGCAA	217325
rs27015819	snp	A/G	0.48	0.0979796	intron-variant	Llgl2	GRCm38.p3	11:115832074	ATAATTAGCTCTCCT[A/G]TAATAGCCATTCCTC	217325
rs27015820	snp	G/T	0.42	0.183303	intron-variant	Llgl2	GRCm38.p3	11:115831637	GGCTAGGCAGGATCA[G/T]CCCCTATCAGACTTC	217325
rs27015821	snp	A/G	0.48	0.0979796	intron-variant	Llgl2	GRCm38.p3	11:115831407	TGAACACATAGGGCC[A/G]AGAGGCTGACCAGTA	217325
rs27015822	snp	C/T	0.231111	0.249285	intron-variant	Llgl2	Mm_Celera	11:115831356	GGTGGGGTTATGTGG[C/T]GGTATCCTAGGCAAA	217325

Full records

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