iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

Llgl2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs261956275	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115849166	GCCTCACCTTGCTTT[A/G]GGCCTACCAGGCAAA	217325
rs262054170	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115850504	AGTGATGACTGTTCC[A/G]CCTCCAGAAATGAGA	217325
rs262066741	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115853459	GACAGGGTCCCCTGG[A/C]TGTCCCTAAGGCACC	217325
rs262190675	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115853161	GGGTAAGTGGTGGAT[A/G]GGAAAACACAGAGGG	217325
rs262215023	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115825984	GGAGGCGTGCTGTCC[A/G]TCCACCATGCTGGCC	217325
rs262260735	snp	A/C			intron-variant	Llgl2	GRCm38.p3	11:115850439	ATCGTCAGGAGCACA[A/C]CCTCTGCTTTTCCTA	217325
rs262281464	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115844406	AGATGCTTGTCTGGG[A/T]GGACCCCTTGCTCCC	217325
rs262298349	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115848790	TGGGAGACTAGGGAA[C/T]TGTCCAGGAAGGAGA	217325
rs262311915	in-del	-/G			intron-variant	Llgl2	Mm_Celera	11:115835503	AGCACCTGAGGGAGT[-/G]GGGGCAGAGTGTGGC	217325
rs262380940	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115845758	GCTCGCCTTTAATGC[C/T]AGCACTTGGGAGGCA	217325
rs262421900	snp	C/T			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115822242	CTATCTAAGGCCTTA[C/T]GGCTGGTTGGTGCCA	217325
rs262427675	in-del	-/CCCCC			intron-variant	Llgl2	GRCm38.p3	11:115844265	AATTGCCTTCCCCAA[-/CCCCC]CCCCCACACACACAC	217325
rs262528932	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115827356	GAAGAACCTGACTAG[A/G]TCTGACAGACAGACC	217325
rs262607899	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115843659	CCCCCCTTGACTTGT[A/G]TACTTGATTGTAGGG	217325
rs262716704	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115838872	AGGCACCCACTAGTA[A/G]CCACACCCCAGTGTG	217325
rs262737285	in-del	-/G			intron-variant	Llgl2	Mm_Celera	11:115833623	GCGCTGAAAGTCAAA[-/G]CCACCCACTCACAGC	217325
rs262792850	in-del	-/T			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115824949	ACCGCGCTGTAGCTC[-/T]TAGAGGGTTTTCACC	217325
rs262829368	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115842712	GAAACCTAGACCTGG[C/T]CACCAGGGTGGCTGG	217325
rs262829534	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115826722	AGCAGGCATCCACAA[A/G]GCAGAATTTGTTAAT	217325
rs262967381	snp	A/C			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823417	AGTTTGTGCTAAAAA[A/C]TATAGCTATTGGCTA	217325
rs263011010	snp	A/T			upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823102	TTCTGCTGTGGTTCA[A/T]TACTTACAGGGGCCC	217325
rs263086811	snp	A/G			missense, nc-transcript-variant	Llgl2	GRCm38.p3	11:115847027	TACAGCCGAGGCCTC[A/G]TCGTCATCTGGGACC	217325
rs263119752	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115846606	GCCCAGATTAGCCTC[C/G]ACTAAGTGTACAACT	217325
rs263188910	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115838516	TGGAGTTAGGGATGG[C/T]TGTGTCCCATCATGT	217325
rs263220634	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115851303	CTCAGCTATCTCCAT[C/T]CAGAAAGCCATAGAT	217325
rs263287910	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115843500	GATCTGGAGAGAGCC[A/G]GTCTTACCCTGCTTC	217325
rs263288438	snp	A/C			intron-variant	Llgl2	GRCm38.p3	11:115845548	GTGAGCTACCCAGTG[A/C]CTTGAGTGTGGGCCA	217325
rs263315145	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115835421	CTCAAGGACCATTCC[C/T]CTGATACTGTCCCCA	217325
rs263409468	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115848640	CTGGCTTAGATGTGG[C/T]CAATCGAAGTCTGGG	217325
rs263417140	in-del	-/A			intron-variant	Llgl2	Mm_Celera	11:115850438	CATCGTCAGGAGCAC[-/A]ACCTCTGCTTTTCCT	217325
rs263429301	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115841479	GAGTTTGAGATTGGA[A/G]ATGTAAGGTGAGGCC	217325
rs263494979	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115842661	AGCTCCTTGCACACC[A/T]ACGGTGAAAAAGGCC	217325
rs263518154	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115834394	TTAGAGCATCAACCA[C/G]GGGGAGAGACAGGCC	217325
rs263619123	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115840366	AGTGGTCACAGTCCT[C/T]GGGACTCTGAAGGAA	217325
rs263688838	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115838082	CTCACACAAAACGGG[A/G]ACGCTGCCCTAGCTA	217325
rs264186843	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115844642	TGGAAGGGATGGGGG[G/T]GGGGGAGCTGGACTC	217325
rs264224183	in-del	-/TGTGTGTGTG			intron-variant	Llgl2	GRCm38.p3	11:115840895	TAAGTTGTTTTGACT[-/TGTGTGTGTG]TGTGTGTGTGTGTGT	217325
rs264408709	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115840076	GAGCCTATGTCCCTT[A/G]TTTTGCTTTTGAGAG	217325
rs264487111	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115837953	AGCGTGTCGTGGGCA[A/T]TGCGTGCAACAACAG	217325
rs264521771	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115834441	AAGGCCTCACTGTCT[C/T]CCTGTCCTGGGCCCT	217325
rs264553233	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115829814	CCTGACTATCTGCCC[C/T]TGAGGGATCTGAACC	217325
rs264601865	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115826910	CTGGGGTGTGGGAGG[A/G]CAGAAGGGGTGCTGC	217325
rs264668263	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115832257	TCTCAGGTGGCCTCC[A/G]CCTGAGCTGATGTGT	217325
rs264687410	in-del	-/A			intron-variant	Llgl2	Mm_Celera	11:115828427	CCGCTGTACAAGGTT[-/A]AGACTTGCCAAGAGG	217325
rs264693286	in-del	-/G			intron-variant	Llgl2	GRCm38.p3	11:115854028	GTTGGGGGAGTGGGA[-/G]GGGGGTCTCAGGCAC	217325
rs264745028	in-del	-/TTTTTG			intron-variant	Llgl2	GRCm38.p3	11:115851436	GAGGAGAGGGGTTTT[-/TTTTTG]TTTTTTTTTTTTTTT	217325
rs264778277	in-del	-/G			intron-variant	Llgl2	GRCm38.p3	11:115828894	CTTTCAGGGGCCTCT[-/G]CAAAGTAGCCATGGG	217325
rs264784794	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115829697	GTAAGAAAAGGAAAT[G/T]ACCAAATCATTGCCC	217325
rs264794077	snp	A/C			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	Mm_Celera	11:115822960	ACGCCCCCACCCCCA[A/C]CCCCCTTGGAACTCA	217325
rs264927063	snp	A/G			synonymous-codon, intron-variant	Llgl2	Mm_Celera	11:115851161	CCCCACAGGCGAGGT[A/G]AGGCCCCAGGCTCAG	217325
rs264987889	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115853594	AGCCTTAGACCCAAA[A/G]GTCAGAGCTAGGAAT	217325
rs264996445	in-del	-/CCTC			intron-variant	Llgl2	Mm_Celera	11:115830022	CAAGGGAGCTCCTGA[-/CCTC]CCTCCCCTCTTTGCT	217325
rs265030141	in-del	-/TGAAGTCAG			intron-variant	Llgl2	Mm_Celera	11:115826849	GATTTTGTGACCTTT[-/TGAAGTCAG]TGGAGCTGAAGATCA	217325
rs265087952	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115846415	ATAAAATTATCCTCT[G/T]AGGGGAGTGGGTTGA	217325
rs265305738	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115826217	GGGAAGATGTCTACA[A/G]ACTGGGGGGCCAAAC	217325
rs265403835	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115842827	GGGTGATCGCACGCA[C/G]ATAACCTGGAAAGCT	217325
rs265509040	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115847476	GTACCCGCTGTGACT[G/T]CCTCAGGGAACTGCA	217325
rs265571822	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115846045	TCTTCTGGCATCTCT[A/G]GGCACCACACACACA	217325
rs265583248	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115837890	ACAGTGGCTACTCAC[C/G]GTGTGGTCACATCTG	217325
rs265667790	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115841948	GTGGTAATGGGGAAA[A/T]GGCTAAATTAAGAGC	217325
rs265677677	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115833741	CTGTTTTCTTTATTC[G/T]GTACAGATAGAATGT	217325
rs265729153	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115839626	TGCTCTGGATTACAG[G/T]GGGGAGGGGACAGGA	217325
rs265844130	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115837108	CACCCTCCTCACTGG[C/T]GATGTCTGGGGCCTG	217325
rs266001854	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115843710	GTCCAAGCTAGTTGT[A/G]TAGTCTTTTGTCCAC	217325
rs266061536	in-del	-/T			intron-variant	Llgl2	Mm_Celera	11:115841118	CAGCCCCGGGAAAGA[-/T]TTTTTTTTATGTTTA	217325
rs266212353	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115838391	GTGGACAGGTTTCAT[G/T]GCTCTATTTATTTTA	217325
rs266223041	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115830459	TCTCCTGATAGCTAA[G/T]GCTAGAGAAGGAAGT	217325
rs386863875	in-del	-/A			intron-variant, downstream-variant-500B	Llgl2	Mm_Celera	11:115855435	CCTGCCCACCTACTG[-/A]TCCTGACCTACTGTC	217325
rs386936698	in-del	-/AACT			intron-variant	Llgl2	Mm_Celera	11:115846454	CTCTCTAGACACTCT[-/AACT]GTCTCAGACATTGCT	217325
rs386946235	in-del	-/CT			intron-variant	Llgl2	Mm_Celera	11:115851535	CAGAAAGTCTGGTGT[-/CT]TAGTCAGGGTTTCTA	217325
rs386984448	in-del	-/CA			intron-variant	Llgl2	Mm_Celera	11:115825386	CTGGCCTTGAACTCA[-/CA]GAGATCCACCTGCCT	217325
rs387126009	in-del	-/T			intron-variant	Llgl2	Mm_Celera	11:115845619	TAGCCTGGGAACTCT[-/T]AAGTAAAACCATCTA	217325
rs387170196	in-del	-/T			intron-variant	Llgl2	Mm_Celera	11:115829598	AAGTCTTTTTTTTTT[-/T]CCAGGAAGGTGTCAA	217325
rs387258429	in-del	-/G			intron-variant	Llgl2	Mm_Celera	11:115854033	GGGAGTGGGAGGGGG[-/G]TCTCAGGCACTGCCA	217325
rs387260926	in-del	-/TCCCTC			intron-variant	Llgl2	Mm_Celera	11:115827032	CTCTCCCTCTCCCTC[-/TCCCTC]CCTCTCTCCCTCTTC	217325
rs387340814	in-del	-/GT			intron-variant	Llgl2	Mm_Celera	11:115846794	TTTGTGTGTGTGTGT[-/GT]TAATATATAGATACC	217325
rs387379523	in-del	-/AACAAAAACACAAAA			intron-variant	Llgl2	Mm_Celera	11:115825860	AAAAAAAGAACAAAA[-/AACAAAAACACAAAA]TTTAGTCTCTCTTAT	217325
rs387448619	in-del	-/CTGTCTGTCTGT			intron-variant	Llgl2	Mm_Celera	11:115827102	TGTCTGTCTGTCTGT[-/CTGTCTGTCTGT]GTCTTCTGTTTCTGT	217325
rs387589113	snp	C/G			intron-variant	Llgl2	GRCm38.p3	11:115852862	CAGATTTCTGAGTTC[C/G]AGGACAGCCAGGGCT	217325
rs387647087	in-del	-/ATTCT			intron-variant	Llgl2	Mm_Celera	11:115830350	ACTAAATAGACTTCT[-/ATTCT]GTTCACAGCCAGCTT	217325
rs387712422	in-del	-/G			intron-variant	Llgl2	Mm_Celera	11:115828772	CCACGCTTTCGGGGG[-/G]CCCCTTCCCGGGCAC	217325
rs387732944	in-del	-/T			intron-variant	Llgl2	Mm_Celera	11:115825896	TAAATTTTATTTTTT[-/T]GTGTGTGCGTAGGTA	217325
rs387744941	in-del	-/A			intron-variant	Llgl2	Mm_Celera	11:115846188	GCTTTCATTAAAAAA[-/A]TGTCCTTTGGGCTAG	217325
rs387756606	in-del	-/AAAC			downstream-variant-500B	Llgl2	Mm_Celera	11:115855998	TAAGGTCCCAGGAAC[-/AAAC]TGAGACCTTATCTGC	217325
rs387782401	in-del	-/CCT			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115822408	TAAGAACCCACACCT[-/CCT]ATCCCTCTACTCTGG	217325
rs387784611	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115826993	CGGGAAAGCCGGGGT[A/G]AAGGATTGAGACTCA	217325
rs387842202	in-del	-/G			intron-variant	Llgl2	GRCm38.p3	11:115850442	TCAGGAGCACAACCT[-/G]CTGCTTTTCCTAGCA	217325
rs387900803	in-del	-/AG			downstream-variant-500B	Llgl2	Mm_Celera	11:115855860	GAGAGAGAGAGAGAG[-/AG]GGAGAGAGAGAGAGA	217325
rs578374373	snp	C/T			downstream-variant-500B	Llgl2	GRCm38.p3	11:115856037	TTCACCCTGGGGGAA[C/T]GAGTGGGTTTATTGG	217325
rs578617749	snp	A/T			intron-variant	Llgl2	GRCm38.p3	11:115837303	GGAGGGTGCAGTGTG[A/T]GTGTGTGTGGAGGGG	217325
rs578724658	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115829421	CCTGGAGATCTCCAC[G/T]TCCTCCTACCCAGGC	217325
rs578989816	snp	A/C			intron-variant	Llgl2	GRCm38.p3	11:115829604	TTTTTTTTTTCCAGG[A/C]AGGTGTCAAGGGGTG	217325
rs578991008	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115846004	ATGGTAGTGCATAAC[C/T]CCAGTTCCAGGGGGA	217325
rs579018465	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115854032	GGGGAGTGGGAGGGG[A/G]GTCTCAGGCACTGCC	217325
rs579173288	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115846022	AGTTCCAGGGGGATC[C/T]GCTGCCCTCTTCTGG	217325
rs579318014	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115837502	AATTCAGAGATCTAC[C/T]TGCCTCCACCTAACG	217325
rs579536814	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115826255	CAGGACAAGCCTCAT[G/T]ATCTTATTTTATGTT	217325
rs579701094	snp	A/T			intron-variant	Llgl2	GRCm38.p3	11:115840871	CAATACAGCTATTAG[A/T]AAGTTGTTTTGACTT	217325
rs579747350	snp	A/T			intron-variant	Llgl2	GRCm38.p3	11:115826965	CCTGACACTTGAAAG[A/T]TCACTTATTCCTCGG	217325
rs579946436	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115831304	GAAAGTAGCAGGGAG[A/G]GGACAGTTGTAGACT	217325
rs580008679	snp	A/T			intron-variant	Llgl2	GRCm38.p3	11:115851675	AGAGGCTGTGGAGGG[A/T]GCTGCTTACTGGCTT	217325
rs580063799	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115831721	AAGGCCTGGGGTGGG[G/T]GAGGGGGCTTTCTGA	217325
rs580179064	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115846718	CTGGCACCTGAGTTT[A/G]CGTGTGTGTGTGTGT	217325
rs580265792	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115850393	TGGTTGGGTGGTTTG[G/T]GGGGGGAGACGGGAA	217325
rs580372789	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115830009	AGGGCTCCTCGGGCC[A/G]AGGGAGCTCCTGACC	217325
rs580383560	snp	G/T			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	GRCm38.p3	11:115822412	AACCCACACCTCCTA[G/T]CCCTCTACTCTGGGC	217325
rs580664158	snp	A/T			intron-variant	Llgl2	GRCm38.p3	11:115841131	AGATTTTTTTTATGT[A/T]TATTTTTTTATTTTT	217325
rs580786973	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115844279	ACCCCCCCCCCACAC[A/G]CACACACCCGTCCTG	217325
rs580878228	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115829419	AACCTGGAGATCTCC[A/G]CGTCCTCCTACCCAG	217325
rs581060272	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115836068	GTATACAGATTGTCT[C/T]CTGCAACAGGACAGC	217325
rs581353583	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115837314	TGTGAGTGTGTGTGG[A/G]GGGGGGGGTGGATAA	217325
rs581583191	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115835947	GGGTTCTGTTCTACT[C/T]TTCCATTTGAGAAGT	217325
rs581622650	snp	C/G			intron-variant	Llgl2	GRCm38.p3	11:115827083	TGTGTGTGTGTGTGT[C/G]TGTCTGTCTGTCTGT	217325
rs581770001	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115846010	GTGCATAACTCCAGT[C/T]CCAGGGGGATCTGCT	217325
rs581934579	snp	A/C			intron-variant	Llgl2	GRCm38.p3	11:115846024	TTCCAGGGGGATCTG[A/C]TGCCCTCTTCTGGCA	217325
rs581985752	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115830176	AATCCCACCACCAAG[A/G]TTGAGGCAGCCCTCC	217325
rs582050524	snp	C/G			intron-variant	Llgl2	GRCm38.p3	11:115829465	CCACGTGAGACAGGG[C/G]TCACCCCTGTGCAGT	217325
rs582142282	snp	A/C			intron-variant	Llgl2	GRCm38.p3	11:115839161	TGCAGGCAGGTGGAT[A/C]TGCCCCTCCTCCCTC	217325
rs582275460	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115846446	GACAGGGTCTCTCTA[G/T]ACACTCTAACTGTCT	217325
rs582379841	snp	A/G			downstream-variant-500B	Llgl2	GRCm38.p3	11:115856042	CCTGGGGGAACGAGT[A/G]GGTTTATTGGATTTC	217325
rs582712965	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115830003	GGTCTGAGGGCTCCT[C/T]GGGCCAAGGGAGCTC	217325
rs582822369	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115845746	AGTTGTGGTGACGCT[C/T]GCCTTTAATGCCAGC	217325
rs582853243	snp	A/C			intron-variant	Llgl2	GRCm38.p3	11:115838053	TAGGCCTTTCCACAG[A/C]GCCAGCAAGATGCCT	217325
rs583092150	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115850394	GGTTGGGTGGTTTGG[G/T]GGGGGAGACGGGAAC	217325
rs583156574	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115835951	TCTGTTCTACTTTTC[C/T]ATTTGAGAAGTATCG	217325
rs583355314	snp	A/T			intron-variant	Llgl2	GRCm38.p3	11:115831707	CTTATCTGGGGTAGA[A/T]GGCCTGGGGTGGGGG	217325
rs583391503	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115831732	TGGGGGAGGGGGCTT[C/T]CTGAACTGAGCCAGG	217325
rs583422455	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115852476	CAGAAACCAGAGCCA[A/G]CACCTGGCTTGATAG	217325
rs583758055	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115841066	ACTCGGGACCTTTGG[A/G]AGAGCAGTCGGCGCT	217325
rs584000133	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115842460	CTGACTGGAGTCTGG[A/G]AGCTGACTCCTTCTG	217325
rs584122236	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115846720	GGCACCTGAGTTTGC[A/G]TGTGTGTGTGTGTGT	217325
rs584229066	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115829420	ACCTGGAGATCTCCA[C/T]GTCCTCCTACCCAGG	217325
rs584381464	snp	A/G			downstream-variant-500B	Llgl2	GRCm38.p3	11:115855861	GAGAGAGAGAGAGAG[A/G]GAGAGAGAGAGAGAG	217325
rs584486706	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115836076	ATTGTCTCCTGCAAC[A/G]GGACAGCTTGTGGTT	217325
rs584725371	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115829472	AGACAGGGGTCACCC[C/T]TGTGCAGTTGCTCTC	217325
rs584824995	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115837321	GTGTGTGGAGGGGGG[G/T]GTGGATAAAGCAGGA	217325
rs584839009	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115852867	TTCTGAGTTCGAGGA[C/T]AGCCAGGGCTACACA	217325
rs585033629	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115846025	TCCAGGGGGATCTGC[C/T]GCCCTCTTCTGGCAT	217325
rs585089883	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115827219	CCTCAAATAAGCGCA[A/G]TCACACTTATTAAAC	217325
rs585103452	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115845862	GAGAAACCCTGTCTC[A/G]AAAACACCAAAAAAA	217325
rs585194683	snp	C/G			intron-variant	Llgl2	GRCm38.p3	11:115846011	TGCATAACTCCAGTT[C/G]CAGGGGGATCTGCTG	217325
rs585429994	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115830278	CGATGCCATAACCTT[C/T]CCGAGGTGATTTCCA	217325
rs585681458	snp	C/G			intron-variant	Llgl2	GRCm38.p3	11:115825376	TGTAGACTAGGCTGG[C/G]CTTGAACTCAGAGAT	217325
rs585693430	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115838250	GGAACTGGAGCCATA[C/T]AGCCGGGCCTTGGTT	217325
rs585796722	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115839188	CCTCCTCCCTCCTCC[C/T]TCCTGAGGCCCTCAG	217325
rs585944796	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115841110	CCATCTCTCCAGCCC[C/T]GGGAAAGATTTTTTT	217325
rs586206964	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115846454	CTCTCTAGACACTCT[A/G]ACTGTCTCAGACATT	217325
rs586255338	snp	A/C			intron-variant	Llgl2	GRCm38.p3	11:115851339	ACTTATGTTAGAGTT[A/C]AGTCCCGAGCAAATA	217325
rs586351866	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115842484	CCTTCTGCACACTGC[A/G]GATTTAGCTCAGTAA	217325
rs586384689	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115847509	GAGGAATCCCCCCCT[C/T]ACAGGCTGACTTGTG	217325
rs586505096	snp	C/G			intron-variant	Llgl2	GRCm38.p3	11:115828417	GAACTGGATGCCGCT[C/G]TACAAGGTTAAGACT	217325
rs586521959	snp	C/G			intron-variant	Llgl2	GRCm38.p3	11:115830006	CTGAGGGCTCCTCGG[C/G]CCAAGGGAGCTCCTG	217325
rs586634802	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115836055	ATGCGGAGGGCTTGT[A/G]TACAGATTGTCTCCT	217325
rs586972982	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115845777	ACTTGGGAGGCAGAC[A/G]TAGGCGGATTTCTGA	217325
rs587113240	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115826362	TGTGGTGTGGGTGCT[A/G]GGAATGGACCTTACG	217325
rs587233120	snp	A/C			intron-variant	Llgl2	GRCm38.p3	11:115827014	TTGAGACTCACTCTC[A/C]CTCTCTCCCTCTCCC	217325
rs587456216	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115833364	CGGTTTAGATAAGAA[A/G]CACCCCCCCTTCCCC	217325
rs864275935	snp	A/C			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	GRCm38.p3	11:115822951	CTGACAGTGACGCCC[A/C]CACCCCCACCCCCCT	217325
rs864293898	snp	A/T			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	GRCm38.p3	11:115822896	GCACACCCTCTTGCC[A/T]GGCCACTGTGCTTTC	217325

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