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
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
rs27015823	snp	A/G	0.231111	0.249285	intron-variant	Llgl2	Mm_Celera	11:115831253	TATGTGGCCGGTAAT[A/G]CCTGTCACCGAGGTC	217325
rs27015824	snp	A/C	0.132653	0.220748	intron-variant	Llgl2	Mm_Celera	11:115831233	CTTAGCCCTGCCCTA[A/C]ACCTTATGTGGCCGG	217325
rs27015825	snp	A/G	0.124444	0.216185	intron-variant	Llgl2	Mm_Celera	11:115831034	TGTGTGGTGAGACCC[A/G]ACGGAGCGGCCTTCC	217325
rs27015826	snp	C/T	0.231111	0.249285	intron-variant	Llgl2	Mm_Celera	11:115830939	TTTTTTGAGTCCTGT[C/T]GCTAGAGGGTCAGAA	217325
rs27015827	snp	G/T	0.231111	0.249285	intron-variant	Llgl2	Mm_Celera	11:115830911	CAGGACGGGCTCAAG[G/T]GATGAGGAAGGCTTT	217325
rs27015828	snp	C/G	0.231111	0.249285	intron-variant	Llgl2	Mm_Celera	11:115830244	TTGGTCCTATGTACC[C/G]TGCAGATAAACCAGA	217325
rs27015829	snp	G/T	0.124444	0.216185	intron-variant	Llgl2	Mm_Celera	11:115830108	CCTGTATCGGGTGGC[G/T]TCCAGTTAACTGAGG	217325
rs27015830	snp	A/T	0.165289	0.235211	intron-variant	Llgl2	Mm_Celera	11:115830014	TCCTCGGGCCAAGGG[A/T]GCTCCTGACCTCCCC	217325
rs27015831	snp	A/G	0.244898	0.249948	intron-variant	Llgl2	Mm_Celera	11:115829702	AAAAGGAAATGACCA[A/G]ATCATTGCCCAGAGG	217325
rs27015832	snp	A/G	0.231111	0.249285	intron-variant	Llgl2	Mm_Celera	11:115829330	GCCCACAGCTCCTGG[A/G]CAGATGGGCCCGGCT	217325
rs27015833	snp	A/G	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115829291	CCTGAGCTATTTAAG[A/G]CCTTTCTTCTAGAGG	217325
rs27015834	snp	A/G	0.459184	0.136902	intron-variant	Llgl2	GRCm38.p3	11:115829188	GAGAGCAGGACTGTT[A/G]CTGGGCATGGCTCCA	217325
rs27015835	snp	C/T	0.124444	0.216185	intron-variant	Llgl2	Mm_Celera	11:115829156	AGGCGAGCTTGAATC[C/T]CACAGTTGTGCTCCT	217325
rs27015836	snp	A/G	0.124444	0.216185	intron-variant	Llgl2	Mm_Celera	11:115828727	GAAGAGGGTTAAGTG[A/G]ACATCTGGGAGATTT	217325
rs27015837	snp	C/T	0.124444	0.216185	intron-variant	Llgl2	Mm_Celera	11:115828628	TAGGATGAGGTTGGC[C/T]TAGGACCAGGTAACT	217325
rs27015838	snp	A/G	0.493827	0.0552116	intron-variant	Llgl2	GRCm38.p3	11:115828584	CTGCTGGGGACAACA[A/G]TTCGTGTTTAAGGAC	217325
rs27015839	snp	C/T	0.336735	0.234472	intron-variant	Llgl2	Mm_Celera	11:115828551	AGACTGGCATGATCC[C/T]CTCTTCCTGGTCACT	217325
rs27015840	snp	A/G	0.231111	0.249285	intron-variant	Llgl2	Mm_Celera	11:115828463	TTTCGAGCTAAAGAC[A/G]TGAGAAGGCAAGACA	217325
rs27015841	snp	A/C	0.260355	0.249785	intron-variant	Llgl2	Mm_Celera	11:115828328	AATATGGCTAATAAT[A/C]ATGCATTTGCAAATG	217325
rs29382351	snp	C/T	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115845006	TACCTTATTGTCCCT[C/T]AGTGCTAGGGTGGGC	217325
rs29384680	snp	A/G	0.48	0.0979796	intron-variant	Llgl2	GRCm38.p3	11:115833920	CACATCTGAAAAGGA[A/G]CATTTCTAGATGCCC	217325
rs29385113	snp	C/T	0.5	0	intron-variant, downstream-variant-500B	Llgl2	Mm_Celera	11:115855319	ATGGGAAGGCGGTCC[C/T]TAAAAGAACTGCCAC	217325
rs29392650	snp	A/G	0.5	0	intron-variant, nc-transcript-variant	Llgl2	Mm_Celera	11:115825139	GTTGTGCTGTGGCCT[A/G]CCTAAAAGAAGGCAA	217325
rs29393209	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	Llgl2	GRCm38.p3	11:115824763	ACACCTTTAGGCGAT[C/G]GTATTGAGTCCCAGT	217325
rs29396400	snp	G/T	0.5	0	intron-variant	Llgl2	Mm_Celera	11:115825659	GGCTGCACCTCTCCA[G/T]TGACAGACTGGTATA	217325
rs29401399	snp	C/G	0.5	0	intron-variant	Llgl2	GRCm38.p3	11:115843256	CCAGCCCCAACCCTG[C/G]GGGATCATGGGGATT	217325
rs29401535	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Llgl2	GRCm38.p3	11:115824843	AGTGAAAAATTGCCA[A/G]AGAAAGTGTGCTATG	217325
rs29402704	snp	G/T	0.444444	0.157135	intron-variant	Llgl2	Mm_Celera	11:115825647	CCTTGAGGCAATGGC[G/T]GCACCTCTCCATTGA	217325
rs29403618	snp	A/G	0.5	0	intron-variant	Llgl2	Mm_Celera	11:115827154	TTCACTCTACACTCC[A/G]TCTAGGGGTAGGGCA	217325
rs29409653	snp	A/G	0.5	0	intron-variant	Llgl2	GRCm38.p3	11:115826397	CTGGAAAAGTTGCAA[A/G]TGGTCTTCACTGTTG	217325
rs29411116	snp	A/C	0.5	0	upstream-variant-2KB	Llgl2	GRCm38.p3	11:115824026	GTATGTAAATCGCGA[A/C]GGCTCCGCCTCCCTC	217325
rs29415527	snp	A/G	0.5	0	intron-variant	Llgl2	GRCm38.p3	11:115835072	ATTTCTGAGACGGGG[A/G]TCTCACCATGTAGCC	217325
rs29418088	snp	C/T	0.5	0	intron-variant, nc-transcript-variant	Llgl2	GRCm38.p3	11:115825125	GTGGAAAGAACCGAG[C/T]TGTGCTGTGGCCTGC	217325
rs29423095	snp	A/G	0.5	0	intron-variant, nc-transcript-variant	Llgl2	GRCm38.p3	11:115825114	AGGAAATGTTTGTGG[A/G]AAGAACCGAGTTGTG	217325
rs29426011	snp	A/G	0.5	0	intron-variant	Llgl2	GRCm38.p3	11:115833502	TTGCTTTCTCTTTCC[A/G]TCTAGAGTGGAATGA	217325
rs29430098	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Llgl2	GRCm38.p3	11:115824790	CAGTCTGTTTTGTAC[A/G]CCGATGAGTGGGGGT	217325
rs29432867	snp	A/G	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115825420	CCTCTCAAGTGCTGG[A/G]ATCAAAGGTGTGCTA	217325
rs29432947	snp	A/G	0.444444	0.157135	intron-variant	Llgl2	Mm_Celera	11:115835486	GGAGGGGGGGGGGGG[A/G]AGAGCACCTGAGGGA	217325
rs29434667	snp	C/T	0.5	0	synonymous-codon, nc-transcript-variant	Llgl2	GRCm38.p3	11:115849655	CACCTGCTCCCACCA[C/T]GTCTCCAACATCCCC	217325
rs29439039	snp	C/T	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115835431	ATTCCCCTGATACTG[C/T]CCCCAAGGAAAAAGC	217325
rs29442956	snp	C/T	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115826278	TTTATGTTAGATTCC[C/T]GTGTATGTGTGCACA	217325
rs29444962	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Llgl2	GRCm38.p3	11:115825055	CGCAACCTCTAGAGA[C/T]CCAGTGTTAAAGTCC	217325
rs29445258	snp	A/C	0.5	0	intron-variant	Llgl2	Mm_Celera	11:115827141	CAGGCTTACTCCATT[A/C]ACTCTACACTCCGTC	217325
rs29459578	snp	C/T	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115826050	AGGTGCCCTTACCTG[C/T]TGAGCCATCTTGCCA	217325
rs29460770	snp	A/G/T	0.5	0	intron-variant	Llgl2	GRCm38.p3	11:115826341	ATCAGAGCCACAGGC[A/G/T]CTTTATGTGGTGTGG	217325
rs29461364	snp	A/G	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115844648	GGATGGGGGTGGGGG[A/G]GCTGGACTCTTCCCT	217325
rs29463594	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Llgl2	GRCm38.p3	11:115824732	GGGAGCCTTTATATT[C/T]CCAGAGCGACTTTGG	217325
rs29468230	snp	C/G	0.5	0	upstream-variant-2KB	Llgl2	GRCm38.p3	11:115823925	GAGCGGCCCCGCTCT[C/G]GAGACTCCCAGGATG	217325
rs29468657	snp	C/T	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115844987	TTCTTTTCTGGCTAC[C/T]CCTTACCTTATTGTC	217325
rs29468867	snp	C/T	0.5	0	intron-variant	Llgl2	GRCm38.p3	11:115825512	GGTAGTTTTCTTGAG[C/T]CATTTCACACAGAAT	217325
rs29470532	snp	C/T	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115825444	TGTGCTAAACTGCTG[C/T]TCCCTCCCCCACCTC	217325
rs29471579	snp	C/T	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115826134	AAAGCTCAAATGAGC[C/T]TGTCCATTACAATGG	217325
rs29477369	snp	C/T	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115844614	CTGCTGCCTTCTTAA[C/T]CCTCACATCTTCTGG	217325
rs29479130	snp	C/G	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115844983	CCCTTTCTTTTCTGG[C/G]TACTCCTTACCTTAT	217325
rs29483006	snp	C/T	0.444444	0.157135	intron-variant	Llgl2	GRCm38.p3	11:115842262	CCTGCCCTGTCTACC[C/T]ACCCTGTCATCCTCA	217325
rs29486611	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	Llgl2	GRCm38.p3	11:115824214	GGACCTTTTGGGGTG[C/G]GAACCACTAGGGGCG	217325
rs45670422	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115826494	GTTATAGAAACACGC[A/G]CATTCAGAAAGCGAG	217325
rs45785335	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115829075	GGGCTGGGGCAGGGT[G/T]GGGGTGGGAGGGTGT	217325
rs45808380	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115846112	GAAGTAAAAATTTTT[A/T]AAATTATTTAAAACA	217325
rs45895538	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115825835	ATACAGAGAAACCCT[A/G]TGTTGGAAAAAAAAA	217325
rs45942189	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115848836	CCAATGAGCATGAGC[C/T]GAGGTCCTTGGGGTG	217325
rs46069735	snp	A/T			intron-variant, nc-transcript-variant	Llgl2	GRCm38.p3	11:115854601	CCTCTCAGGCTGCTG[A/T]GTGGGGGTACACCTG	217325
rs46080585	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115848957	CACCCTCTCCATGTG[G/T]TTGCTGGGAATTGAA	217325
rs46121379	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115854125	CCCCTGGGAGGGAGG[C/T]CCTGTCTCAGCCACA	217325
rs46136657	snp	C/T			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	GRCm38.p3	11:115822787	ACTGCTCTCAGGGGC[C/T]GTGCCAGCTGTCTCT	217325
rs46412750	snp	A/C			intron-variant, nc-transcript-variant	Llgl2	GRCm38.p3	11:115854984	GCCAGGGACAAGCCT[A/C]TCAGGGACCCCACTG	217325
rs46474931	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115847412	AGAAGCAGAATCTGG[A/G]CCCAGAGAGGTTCGG	217325
rs46506889	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115825457	TGCTCCCTCCCCCAC[C/T]TCCCCCAAACCCCCT	217325
rs46591692	snp	G/T			intron-variant, downstream-variant-500B	Llgl2	GRCm38.p3	11:115855342	ACTGCCACCCCTCCA[G/T]GGCCCAACAGGCCTC	217325
rs46615790	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115850965	CTGGGACCTTGTGAC[C/T]CTGTAGCGTTGATGG	217325
rs46742046	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115848435	CCTTTGGGTCCCTTG[A/G]CCTTATTATCCTTCT	217325
rs46810261	snp	C/T			missense, nc-transcript-variant	Llgl2	GRCm38.p3	11:115854328	GCAATGGCACAGGCC[C/T]CAAAATGACCTCCTC	217325
rs46903229	snp	C/T			intron-variant, downstream-variant-500B	Llgl2	GRCm38.p3	11:115855334	TTAAAAGAACTGCCA[C/T]CCCTCCAGGGCCCAA	217325
rs46963260	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115852883	AGCCAGGGCTACACA[G/T]AGAAACCCTGTCTCA	217325
rs46972037	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115847348	TTGTCTTCTGCCTGA[A/G]AAGCACCTGTGGGCT	217325
rs47166327	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115848400	GAAGACCTCTGTGTA[A/G]ATGTTCCCTAACCTG	217325
rs47295561	snp	C/T			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	GRCm38.p3	11:115822272	ATGGGAACCCAAGAT[C/T]CCCCATCCTTGGCTC	217325
rs47361206	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115851728	TGCTTTCTTGTAGAA[C/T]CCAGGACCACCAGCC	217325
rs47378810	snp	C/G			intron-variant	Llgl2	GRCm38.p3	11:115853254	TGCCTCTTCCCCACC[C/G]CCCTCCTCTGTAGCC	217325
rs47490418	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115846652	CACCTGATCTTTCTA[C/T]CTCCTAAGTTTGAGG	217325
rs47505892	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115853551	GCCACAGGATCACAG[A/G]AAATAAGGAAGGGAT	217325
rs47587491	snp	A/C			intron-variant	Llgl2	GRCm38.p3	11:115826935	TGCTGCCTCTTCTAG[A/C]CTTGACACCTCTTCC	217325
rs48385240	snp	C/T			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	GRCm38.p3	11:115822987	CTCAGGACTTGTTTT[C/T]AGAGGCCCAGGACTT	217325
rs48393020	snp	A/C/G			downstream-variant-500B	Llgl2	Mm_Celera	11:115856219	ACTTGGTTGAGGAAC[A/C/G]CCCCCCTCCCCCAGT	217325
rs48435693	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115854000	TGGAGGCACGGCCTG[G/T]GGCCTCTGTGAGGTT	217325
rs48493619	snp	C/T			synonymous-codon, nc-transcript-variant	Llgl2	GRCm38.p3	11:115852227	GGAGGACTCCTTCAC[C/T]GGCTTTGTCCGGACC	217325
rs48570630	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115848872	TGCTTCCTCCAGATG[C/T]TCCTGCCTGAGTCTT	217325
rs48648953	snp	A/G			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	GRCm38.p3	11:115823264	TCCAATCTTGGTCCT[A/G]CCCTGAGGACCAACA	217325
rs48796866	snp	A/G			intron-variant, nc-transcript-variant	Llgl2	GRCm38.p3	11:115854644	CTAGCCTGGGGTAAA[A/G]GAGGAGAGGGGCTGA	217325
rs48921986	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115848389	GATGCAAAAATGAAG[A/G]CCTCTGTGTAGATGT	217325
rs49063018	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115825325	TCATTCAGACAGGGT[G/T]TTTCTGTGTAGCCCT	217325
rs49111612	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115851702	GCTTGCTCCTCATGG[C/T]TTGCTCAGCCTGCTT	217325
rs49159109	snp	A/G			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	Mm_Celera	11:115822851	CCATTGGGGTCTGTG[A/G]TCCTAGGTGTCTTCT	217325
rs49209607	snp	G/T			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	Mm_Celera	11:115822755	CTCTGGGGATGGCTT[G/T]CTCTGGGGGGGCCTG	217325
rs49269514	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115851795	CCATATCAACCACTA[A/G]TTAAGAAAATTCTCT	217325
rs49374356	snp	C/T			downstream-variant-500B	Llgl2	Mm_Celera	11:115856226	TGAGGAACACCCCCC[C/T]CCCCCAGTTTAGCTC	217325
rs49470756	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115846159	CAGCAACTTAAATTC[C/T]AGTAAATGTTACTTG	217325
rs49630878	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115853470	CTGGATGTCCCTAAG[A/G]CACCAGCAGTGTTCA	217325
rs49861931	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115847845	CCTTCAACCTTCCCA[A/G]AGAGGTGCTGTTGGC	217325
rs49875795	snp	C/T			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	Llgl2	GRCm38.p3	11:115855614	AGCTCCCACCGGGGC[C/T]GCCCCTCCTGGGCCC	217325
rs49957800	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115852849	AGGCAGTGGCAGGCA[G/T]ATTTCTGAGTTCGAG	217325
rs49987535	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115848925	GGGAGACCCTAGGCC[C/T]GTGTTTGCTTCTTTC	217325
rs50104470	snp	A/C			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	GRCm38.p3	11:115823445	CTATAGGGGCTGACA[A/C]CCCCCTTGAACCTCA	217325
rs50207240	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115846195	ATTAAAAAATGTCCT[C/T]TGGGCTAGGCAGATG	217325
rs50222919	snp	A/T			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	GRCm38.p3	11:115823077	CAAAGCCATTAAAAA[A/T]ATATATATTTTCTGC	217325
rs50308350	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115846111	TGAAGTAAAAATTTT[A/T]TAAATTATTTAAAAC	217325
rs50331554	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115826121	AATAAATAAAGGGAA[A/G]GCTCAAATGAGCCTG	217325
rs50350725	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115828016	AGTATCCCGAAGCCA[C/T]AGTCTGTGACAGGGC	217325
rs50422700	snp	C/G			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	GRCm38.p3	11:115822958	TGACGCCCCCACCCC[C/G]ACCCCCCTTGGAACT	217325
rs50464005	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115848574	GATTTGGCCCAACTC[A/G]GGCACATCTGTGTTG	217325
rs50497423	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115848975	GCTGGGAATTGAACT[C/T]GGGACCTCTGGAAGA	217325
rs50531054	snp	C/T			synonymous-codon, nc-transcript-variant	Llgl2	GRCm38.p3	11:115848282	CCAGCAGACGGCCTT[C/T]GACTTCACCTCCCGT	217325
rs50645089	snp	A/C			intron-variant	Llgl2	GRCm38.p3	11:115849968	AGACACCCTGTCTGA[A/C]GTAGCCCTCACCAGG	217325
rs50709734	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115849963	ACCCCAGACACCCTG[G/T]CTGAAGTAGCCCTCA	217325
rs50722275	snp	C/T			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	GRCm38.p3	11:115822807	CAGCTGTCTCTCATA[C/T]AGGACTCACCTGGAT	217325
rs50753338	snp	C/T			intron-variant, nc-transcript-variant	Llgl2	GRCm38.p3	11:115854657	AAGGAGGAGAGGGGC[C/T]GAGGGTGAGTGAGAG	217325
rs50959062	snp	C/T			intron-variant, nc-transcript-variant	Llgl2	GRCm38.p3	11:115854742	TCCAGCGCTCCCTCC[C/T]TTAACCCCTGTAATG	217325
rs51117706	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115849936	ATGGTAGGTGGGAGC[A/G]GAACCCTGGAGACCC	217325
rs51124894	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115847443	GGCTTGGCCCAAAGC[C/T]ACACAGCTGGTTTTC	217325
rs51180307	snp	A/G			synonymous-codon, nc-transcript-variant	Llgl2	GRCm38.p3	11:115854323	CAATGGCAATGGCAC[A/G]GGCCTCAAAATGACC	217325
rs51517729	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115848956	TCACCCTCTCCATGT[A/G]TTTGCTGGGAATTGA	217325
rs51589173	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115844358	ATGACCACTGCTATC[C/T]ACCCCCACCCTGTGC	217325
rs51594471	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115852971	GGAAGCCCGGGTTGC[C/T]GGCCCCACTCAACCC	217325
rs51597519	snp	A/C			intron-variant	Llgl2	GRCm38.p3	11:115848372	AGTTTGGGTGCTGGG[A/C]AGATGCAAAAATGAA	217325
rs51796552	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115846090	ACATAAAATAATTAC[A/G]TCTAATGAAGTAAAA	217325
rs51881985	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115848099	GGCTTTGCCCTGTAT[A/G]CTCCATCAGGTCCCA	217325
rs52022512	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115843253	AGCCCAGCCCCAACC[C/T]TGGGGGATCATGGGG	217325
rs52063266	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115848532	TTCCAGGCCACACCT[C/T]TTGCCTGTCCCAATC	217325
rs52164743	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115827044	CTCTCCCTCCCTCTC[C/T]CCCTCTTCCCCTCTC	217325
rs52210538	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115825954	TGTGTGTTTGTGTAG[A/G]CCAAAGGACAAGTTG	217325
rs52214477	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115850375	GTGGGGTTGAGGGCA[A/G]AGTGGTTGGGTGGTT	217325
rs52248501	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115825899	AATTTTATTTTTTGT[A/G]TGTGCGTAGGTATGT	217325
rs52251351	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115825904	TATTTTTTGTGTGTG[C/T]GTAGgtatgtgtgtg	217325
rs52258492	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115850404	TTTGGGGGGGGAGAC[A/G]GGAACCCCTGCCCGA	217325
rs52299503	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115851472	TTGGTTTGCACTGCA[A/C]CCTACCATACAAATA	217325
rs52343147	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115846776	TACACGTGCATGCAT[A/G]TGTTTGTGTGTGTGT	217325
rs52425596	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115827043	CCTCTCCCTCCCTCT[C/T]TCCCTCTTCCCCTCT	217325
rs52440277	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115846786	TGCATATGTTTGTGT[A/G]TGTGTGTGTTAATAT	217325
rs52517177	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115825853	TTGGAAAAAAAAAAA[A/G]AACAAAATTTAGTCT	217325
rs52566544	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115826988	TTCCTCGGGAAAGCC[A/G]GGGTGAAGGATTGAG	217325
rs107622177	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115852832	TAATCCCAGCACTTA[A/G]GAGGCAGTGGCAGGC	217325
rs107820921	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115831471	CCCCAGCGCCCTTGA[C/T]CTCAGCATCTTGTAT	217325
rs107837872	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115852840	GCACTTAGGAGGCAG[A/T]GGCAGGCAGATTTCT	217325
rs211718294	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115842061	GCTTGTCCCACACAG[C/T]CTGTGTGATTTCTCT	217325
rs211734870	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115833019	CTAAAAATGTGAAAT[C/T]CCTAGTCTCTCTCCC	217325
rs211760105	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115833829	AGGAAATAGGGTCTC[A/G]CTTTGTACCCTTCAT	217325
rs211798863	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115826483	GGAAATCCATTGTTA[C/T]AGAAACACGCACATT	217325
rs212042866	in-del	-/C			intron-variant	Llgl2	Mm_Celera	11:115830190	GGTTGAGGCAGCCCT[-/C]CCCTGTCCATCACAC	217325
rs212102043	in-del	-/GA			downstream-variant-500B	Llgl2	Mm_Celera	11:115855827	GGTCCATCTCCAGCC[-/GA]GAGAGAGAGAGAGAG	217325
rs212139734	snp	C/T			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115825070	TCCAGTGTTAAAGTC[C/T]ATTCTGAGCTAGATG	217325
rs212203769	snp	A/G			downstream-variant-500B	Llgl2	Mm_Celera	11:115856038	TCACCCTGGGGGAAC[A/G]AGTGGGTTTATTGGA	217325
rs212213488	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115855145	ATGTGGGGACATGGG[A/G]GATGAGGCCACCCGT	217325
rs212255111	snp	A/G			missense, nc-transcript-variant	Llgl2	Mm_Celera	11:115853882	GGTGACATCCAGGTG[A/G]TCTCAATGCCCCTGC	217325
rs212340937	in-del	-/TTCTA			intron-variant	Llgl2	Mm_Celera	11:115830346	TCTCACTAAATAGAC[-/TTCTA]TTCTGTTCACAGCCA	217325
rs212485429	snp	A/G/T			intron-variant	Llgl2	Mm_Celera	11:115841294	TGGATGCTGGGAATC[A/G/T]AACACAGATCCTCTG	217325
rs212499235	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115853442	AATTCAAGGTGCCAC[A/G]TGACAGGGTCCCCTG	217325
rs212639422	snp	C/T			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115850737	GGGGCACGAGCGCCT[C/T]GCCGCCCGCCCGGGG	217325
rs212754486	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115845741	TGGCTAGTTGTGGTG[A/G]CGCTCGCCTTTAATG	217325
rs212878699	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115849433	CAGATTGATGGCTCC[A/T]GCTCCCCAGCCTGGA	217325
rs212892644	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115837552	AGATTAAAGGCTCAC[A/G]GTATACCCCACTGTG	217325
rs212975610	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115843273	GGATCATGGGGATTC[A/G]AAGGACTCGCCTATA	217325
rs213060904	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115851377	TTGTTGTCTGAGTCA[C/G]GTCACTGTTGCTGAG	217325
rs213108630	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115843787	CCCTGGGACAACTTC[C/T]CTGAAGTCCTGGACA	217325
rs213114867	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115835099	AGCCCTGACTGGCCT[A/G]GAACTCACAGAGATC	217325
rs213126576	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115827762	TCTCCGTCTGCCCTG[A/C]CTCAGAGAAAACTGG	217325
rs213149523	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115835755	TCTCCAGGGCATGTC[C/T]GTAGGTGCAATTCTG	217325
rs213360147	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115838780	ACTACCTCAGGGGCT[A/G]GACGGACGTCCTGGT	217325
rs213362108	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115850171	CCGGGAGCCTGGGAG[C/T]CAGGGGTGCAGGGAC	217325
rs213372358	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115847736	ACAGTGCCCACTGAG[A/G]ACACAAGGATCGTGG	217325
rs213482046	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115830810	TTGACCTGGGCTTTG[A/G]AGGTCAAGCTCGGGT	217325
rs213520444	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115831331	GACTGGGGCGAGGGA[A/G]CATTTGAGCGGTGGG	217325
rs213658715	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115828382	ACCAAAGAAGAGGGC[A/G]GGATGTGCCACAATG	217325
rs213685144	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115825786	GCTCGAGGCCAGCCT[A/G]GTCTACAGAATGAGT	217325
rs213702667	in-del	-/CCCCGA/CCCGA/CGA			downstream-variant-500B	Llgl2	Mm_Celera	11:115856227	AGGAACACCCCCCTC[-/CCCCGA/CCCGA/CGA]CCCCAGTTTAGCTCT	217325
rs213716239	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115849357	CAGCAGCAGCCTCGT[C/T]GCGAGGCCTTGGTCG	217325
rs214072616	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115834723	GATTCTGGCCCCAGG[A/G]AGCTGTGGGTCTGGG	217325
rs214077303	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115826532	GCAGAAGGGGATTCC[G/T]TTGCCTGTCGTCTTT	217325
rs214234701	snp	A/C			downstream-variant-500B	Llgl2	Mm_Celera	11:115855803	AGGACCCGTGCTTCT[A/C]TGTGCTTCTGGTCCA	217325
rs214277425	in-del	-/CAAAT			intron-variant	Llgl2	Mm_Celera	11:115838971	CACCACCACACCTCC[-/CAAAT]CAAATAAATGGTGTG	217325
rs214311599	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115829843	CCGGGAGATGGCTCA[C/T]GGGCTGGGCTGGTTT	217325
rs214351591	snp	A/G			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823269	TCTTGGTCCTGCCCT[A/G]AGGACCAACAGCTGG	217325
rs214558851	snp	A/G			synonymous-codon, nc-transcript-variant	Llgl2	GRCm38.p3	11:115852212	TGAGGCTCGCTCCGC[A/G]GAGGACTCCTTCACT	217325
rs214632803	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115841332	AGTCTCTTAATGGAC[C/T]AGCCATCACTCCAGT	217325
rs214770091	in-del	-/AACA			downstream-variant-500B	Llgl2	Mm_Celera	11:115855995	TCCTAAGGTCCCAGG[-/AACA]AACTGAGACCTTATC	217325
rs214774499	snp	A/C			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115850271	TACAGCGATGATCCG[A/C]GGCTAGGCATCCAGA	217325
rs214809699	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115833891	GTGACCTAGGTTACA[C/T]GTGTGCCACCATGCA	217325
rs215005898	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115852104	CCCTTAGACCTAGCC[C/T]AACTTCCTGCAGGCG	217325
rs215019029	in-del	-/ATTG			intron-variant	Llgl2	Mm_Celera	11:115833238	AGTCTTGGCCCTTTA[-/ATTG]ATTGATTACAGAGCT	217325
rs215039176	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115849033	ACCTCTCCAGCCCCC[C/T]CCTCCCCTCTTATTG	217325
rs215081408	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115842275	CCCACCCTGTCATCC[C/T]CAGGGATCCCCTAAA	217325
rs215203734	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115830037	ACCTCCCCTCTTTGC[A/T]GGTTCTTAGTTCCTG	217325
rs215272016	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115835799	TGAGGATTGAGCCCA[A/G]ACCATCTCAGTAACC	217325
rs215402360	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115827848	AGAGGCTCCTTTGGG[C/T]GTGGGGACAGGGAAG	217325
rs215442670	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115828402	GTGCCACAATGGATA[A/G]AACTGGATGCCGCTG	217325
rs215460218	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115845765	TTTAATGCCAGCACT[C/T]GGGAGGCAGACATAG	217325
rs215502955	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115837618	CATGGTGAAGCATCT[A/G]GTCCAATGACGAGTA	217325
rs215667363	snp	A/G			intron-variant, nc-transcript-variant	Llgl2	Mm_Celera	11:115825246	GATGTCTCAACAAAT[A/G]AGTCAGGTAATTTTC	217325
rs215701163	in-del	-/GAAAAAAAACAAAAAAC			intron-variant	Llgl2	GRCm38.p3	11:115825847	CTGTGTTGGAAAAAA[-/GAAAAAAAACAAAAAAC]AAAAAGAACAAAATT	217325
rs215787882	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115843911	ATCTCCTGCCACAAA[A/G]TCCTCCCCCTAGGCT	217325
rs215798366	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115825807	CAGAATGAGTTCCAG[A/G]ATATCCAATGCTATA	217325
rs215973448	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115830675	TGACCTGGAACTCAC[C/T]TTGCACAGTGAGCCA	217325
rs215975258	snp	A/C			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823423	TGCTAAAAACTATAG[A/C]TATTGGCTATAGGGG	217325
rs215980151	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115846196	TTAAAAAATGTCCTT[A/T]GGGCTAGGCAGATGG	217325
rs215999311	in-del	-/T			intron-variant, downstream-variant-500B	Llgl2	Mm_Celera	11:115855431	CCTTCCCTGCCCACC[-/T]ACTGTCCTGACCTAC	217325
rs216008725	snp	A/G			upstream-variant-2KB	Llgl2	Mm_Celera	11:115824025	TGTATGTAAATCGCG[A/G]AGGCTCCGCCTCCCT	217325
rs216031250	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115838035	CAGCTTCTAAACCAG[G/T]TCTAGGCCTTTCCAC	217325
rs216143732	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115852764	GTCCATTTTAGAGGA[A/G]GGAACTGAATCTTTA	217325
rs216264140	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115844962	CAGGGTAAGAGCATA[A/G]TGGCCCCCTTTCTTT	217325
rs216311687	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115840943	TTTTTTTAATTAATT[A/T]ATTTATTTATATGTA	217325
rs216358728	snp	A/C			intron-variant, nc-transcript-variant	Llgl2	Mm_Celera	11:115832777	CACCACCCTCCCCCA[A/C]GGCTGGAATGTTCAG	217325
rs216376521	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115827675	GAGATGGGTGTTGCC[C/T]ATCAGCCACTGTACT	217325
rs216529179	in-del	-/CCC			intron-variant	Llgl2	GRCm38.p3	11:115826457	AAAAAAAAAAAAAAA[-/CCC]GAGGGAATGGAAATC	217325
rs216534504	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115850370	GCAGGGTGGGGTTGA[A/G]GGCAGAGTGGTTGGG	217325
rs216571705	snp	C/T			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115850668	GGCGGCCGAGCATGC[C/T]GTGGAGCAGGTGGAG	217325
rs216589984	snp	A/G			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115822468	TGGAGTTTGCAGAAG[A/G]CAGAGCCCAGAGGCC	217325
rs216637286	in-del	-/TTTTC			intron-variant	Llgl2	Mm_Celera	11:115834248	TATGTTTTTTTTTTT[-/TTTTC]CTTTCAGAAAACAGG	217325
rs216697344	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115844994	CTGGCTACTCCTTAC[C/T]TTATTGTCCCTCAGT	217325
rs216707534	snp	A/C			intron-variant, nc-transcript-variant	Llgl2	Mm_Celera	11:115854993	AAGCCTCTCAGGGAC[A/C]CCACTGGTAAAGGAG	217325
rs216741349	snp	A/G			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	Llgl2	Mm_Celera	11:115855490	TGGGACAGCACCCAG[A/G]CTGTGGGATGATCAC	217325
rs216742623	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115849057	CTTATTGCGCCGGCT[A/G]CCTAGAGCTACCCCT	217325
rs216752801	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115840019	GGCTTGGCCTCCTCT[A/G]AGGAGTCAGCTCATG	217325
rs216870249	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115849385	TCGTGGCACTTCAGC[G/T]TATTGCTCTTATTTT	217325
rs216904755	in-del	-/CTGCCGCAG			intron-variant	Llgl2	Mm_Celera	11:115829963	TGGTGATTCAAATGA[-/CTGCCGCAG]CTCCTTCTTGGTGTC	217325
rs216971473	snp	C/G			intron-variant	Llgl2	GRCm38.p3	11:115827079	TGTGTGTGTGTGTGT[C/G]TGTCTGTCTGTCTGT	217325
rs217097297	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115846257	GAACACTAGACTTCA[C/G]TTCCCAACACCCACA	217325
rs217098762	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115852622	CTGATTTTTCCCTGC[A/T]GGCTGTGAGCGGTGT	217325
rs217101658	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115847141	CCCGATCGATCCCAG[C/T]CTCTCATCTCTTCCT	217325
rs217188953	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115846788	CATATGTTTGTGTGT[A/G]TGTGTGTTAATATAT	217325
rs217347238	snp	A/G			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115824216	ACCTTTTGGGGTGCG[A/G]ACCACTAGGGGCGGC	217325
rs217471081	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115845591	GGGCCCCAGTAAGGA[C/T]TATTTGCCATGTCTA	217325
rs217532976	snp	C/T			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823205	TGCCCAGGGCTGTGA[C/T]CATGGAGTTGATGGA	217325
rs217629134	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115847811	ACGGTCTCTGCAAAA[G/T]CCCCTCCTTCCATCC	217325
rs217944101	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115848763	AGACAAGACAAGGGT[A/T]GACATAGACCCTGGG	217325
rs217975202	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115849108	AAGCAGTTCACATGC[A/G]GAGGCCGCTCTGTGG	217325
rs217975448	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115841585	TGTTGTTGTTGTTTT[A/G]TAGTTGTTTGATTTT	217325
rs218311945	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115846387	CACACACATGTGTAC[A/G]TGATTAAAAACAATA	217325
rs218373136	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115839077	GTGTCAGATGACAAC[C/T]ACACAGAGAGGCCAA	217325
rs218375325	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115842562	AGTCAGTGCCGTAGG[A/G]TAGGTAGCTGTTGGG	217325
rs218393392	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115843209	GCAGAGCTCAGAGCC[C/T]CCTTTCCCTGATTGA	217325
rs218400656	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115840090	TGTTTTGCTTTTGAG[A/G]GAGCCTTGGTCCCTC	217325
rs218445722	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115834945	GAAACCCTGGCCTGG[A/G]CTCCTCCCCAGGGGC	217325
rs218514827	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115835680	CGTCTGCTTTGATCT[A/G]TGTCCGAAGTAGATT	217325
rs218656317	snp	A/C/G			intron-variant	Llgl2	Mm_Celera	11:115843624	GTTACTCACGTCCCC[A/C/G]TTCCCCCCCCCCCCG	217325
rs218706229	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115842603	CCAGGCCTGCTGAGC[A/G]ATGCTTTGACATCAG	217325
rs218723728	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115835999	TCCAAAGACATCTTT[C/T]CTGCTTATGAACGAA	217325
rs218759991	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115836920	GTAAAGTCAGATTCC[A/G]GAGTACTTGAGACCC	217325
rs218927887	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115838116	CCATGAGGGTTACCT[A/G]TCCTTGGCCAGGAGT	217325
rs218965585	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115830706	CAGGGGTCCGCCTCC[C/T]GGAACTCGCTGTGAG	217325
rs219076133	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115838225	TGGGTGTTAACAGTG[G/T]TTGGGGCAGGGAACT	217325
rs219091914	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115831262	GGTAATACCTGTCAC[C/T]GAGGTCCTGAGTAGG	217325
rs219105751	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115830374	CCAGCTTTCTGTTGC[A/G]GGTCTGAGCCCCTTC	217325
rs219201208	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115837427	ACTTTTTTGAAGACA[A/G]GGTCTCATTATGTAG	217325
rs219249850	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115829093	GGTGGGAGGGTGTCC[A/G]ATAGATCAGTGACAT	217325
rs219261602	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115836789	CTTAGGGAGGGGAAG[A/G]GCTGAGGGCCTCACA	217325
rs219720706	in-del	-/TC			intron-variant	Llgl2	Mm_Celera	11:115842471	TGGAAGCTGACTCCT[-/TC]TCTGCACACTGCGGA	217325
rs219724091	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115837811	CCACAGAATCAAAGG[C/T]GCATGGGCTGTTGTC	217325
rs219846924	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115853550	GGCCACAGGATCACA[A/G]AAAATAAGGAAGGGA	217325
rs219879779	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115825277	TTTTCTCTTTAAATA[C/T]TTATTTGTTTGTTTG	217325
rs220024764	in-del	-/T			intron-variant	Llgl2	Mm_Celera	11:115845618	CTAGCCTGGGAACTC[-/T]TAAGTAAAACCATCT	217325
rs220041020	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115834364	CTCCTGTTCCCATTA[G/T]GGTAACTGGTGGCAT	217325
rs220098160	snp	A/G			intron-variant, downstream-variant-500B	Llgl2	Mm_Celera	11:115855307	TGCCAGGGAGGGATG[A/G]GAAGGCGGTCCTTAA	217325
rs220206119	in-del	-/T			intron-variant	Llgl2	Mm_Celera	11:115849099	TTCCTTGACAAGCAG[-/T]TCACATGCAGAGGCC	217325
rs220447099	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115839527	GAGAACTGCAGAGCG[G/T]TGGTCCACCTTCTTG	217325
rs220478400	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115840319	CCTGACTGGGTGCCT[A/G]TTCTCAACTGGCCTT	217325
rs220515657	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115831974	AGCAGTGACCAGGCA[C/T]CTGGTCCCAAACTGC	217325
rs220608956	snp	C/T			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115824624	GCTTAGTTCTTACCT[C/T]TGCCATCTGGGCGCT	217325
rs220705711	in-del	-/TTA			intron-variant	Llgl2	Mm_Celera	11:115827226	TAAGCGCAATCACAC[-/TTA]TTAAACATCTCTCTC	217325
rs220795877	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115835293	CAGGTACAAAACTTT[C/T]AGCCCTGCCTGCTTT	217325
rs220796096	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115826741	GAATTTGTTAATTTT[C/T]CTTGAAGCATGGAAA	217325
rs220831827	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115827374	TGACAGACAGACCCT[C/G]CGACCTTGTGGGGAG	217325
rs220847423	in-del	-/CC			intron-variant	Llgl2	Mm_Celera	11:115826249	GGCCTACAGGACAAG[-/CC]TCATGATCTTATTTT	217325
rs220962316	snp	C/T			downstream-variant-500B	Llgl2	Mm_Celera	11:115855979	GTCTGTCTGTCCCTC[C/T]TCCTAAGGTCCCAGG	217325
rs220973022	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115835486	AGGAGGGGGGGGGGG[A/G]AGAGCACCTGAGGGA	217325
rs221000466	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115849935	CATGGTAGGTGGGAG[A/C]GGAACCCTGGAGACC	217325
rs221040933	snp	A/G			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	Mm_Celera	11:115822848	AGGCCATTGGGGTCT[A/G]TGATCCTAGGTGTCT	217325
rs221089624	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115845720	CTCATTTAAAGATGA[A/G]AGAAGTGGCTAGTTG	217325
rs221116842	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115850441	CGTCAGGAGCACAAC[C/T]TCTGCTTTTCCTAGC	217325
rs221152710	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115830822	TTGAAGGTCAAGCTC[C/G]GGTCCTCATGCTTTT	217325
rs221152826	snp	C/G			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823559	CATACCACTTTACTA[C/G]TGGGTCTGAAACCTG	217325
rs221190961	snp	A/G			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115824514	AGAGACACCGTTCCC[A/G]GACCCTTGTGCGAGG	217325
rs221252233	in-del	-/C			intron-variant	Llgl2	Mm_Celera	11:115828773	CACGCTTTCGGGGGG[-/C]CCCTTCCCGGGCACT	217325
rs221277274	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115845941	GAGAGGTGGCTCAGA[A/G]CAATGTCTGTTTTTG	217325
rs221310634	in-del	-/T			intron-variant	Llgl2	GRCm38.p3	11:115851441	AGGGGTTTTTTTTTG[-/T]TTTTTTTTTTTTTTT	217325
rs221328554	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115828156	GTGACTAGAGAAGAC[C/T]ATGCCTAGCTAATCC	217325
rs221435157	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115848051	TTCAGGCCTTGGGAT[C/T]CCTCAGCCTCCCGAC	217325
rs221667919	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115834183	GGACAGCCCCGCTTC[C/T]GCCAACCCACTGCAC	217325
rs221711931	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115830396	AGCCCCTTCACGGGG[G/T]GGGGGTGGGGGGGTC	217325
rs221769350	in-del	-/C			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115824553	CGCAGAGCGGGGCGA[-/C]CCGGCTTCCTGTGAC	217325
rs221887627	snp	A/T			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823555	TTCCCATACCACTTT[A/T]CTAGTGGGTCTGAAA	217325
rs221894986	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115826589	AGGCATCAGATGACT[A/G]TGAATCCTACCTTCC	217325
rs221964792	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115827446	TGAGACTCCTGAGCT[A/G]GGTACCACGGGAGGC	217325
rs221983937	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115848651	GTGGTCAATCGAAGT[C/T]TGGGTGGGGTAGCAG	217325
rs222040370	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115851873	GGTTCTCTCCTCTCA[A/G]ATGACGTTCACCTGT	217325
rs222047008	in-del	-/AGTGGGGTTGCTAAGCACCCT			intron-variant	Llgl2	Mm_Celera	11:115838339	TTTCCTCTTCCGTGA[-/AGTGGGGTTGCTAAGCACCCT]AATGGAGGCTGGTGC	217325
rs222109327	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115852949	AGATTCGGTAGCAAG[A/G]CTGGGTGGAAGCCCG	217325
rs222142518	snp	A/T			downstream-variant-500B	Llgl2	Mm_Celera	11:115855940	TGCTAACTTTCCAGG[A/T]GTAGGGGTGACTATG	217325
rs222188003	snp	A/G			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115822143	TGAGCAGTGCCTCTG[A/G]CTGCTGCCAGCCCAT	217325
rs222345223	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115845783	GAGGCAGACATAGGC[A/G]GATTTCTGAGTTCAA	217325
rs222427568	snp	A/G			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115824495	TGCGGGGGACACAGT[A/G]AGCAGAGACACCGTT	217325
rs222437625	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115849264	CAAACATTAGGAAGA[A/G]TTTCCCAGTGGCTTG	217325
rs222470067	snp	C/T			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115849691	GCTATGGGAACGCAT[C/T]ATCGCCGCGGGCAGC	217325
rs222673668	in-del	-/TG			intron-variant	Llgl2	Mm_Celera	11:115844642	GGAAGGGATGGGGGT[-/TG]GGGGGAGCTGGACTC	217325
rs222763776	snp	C/G			missense, intron-variant	Llgl2	Mm_Celera	11:115851179	GCCCCAGGCTCAGAG[C/G]AGCCATCTACAGGAC	217325
rs222789648	in-del	-/CGG			intron-variant	Llgl2	Mm_Celera	11:115830846	GCTTTTGCAAGATAA[-/CGG]CTTTTCTGGCTGAGC	217325
rs222822817	snp	A/G			upstream-variant-2KB, synonymous-codon, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115822062	GGCTGACGCTGTGGC[A/G]ACGTTCCGAAAAAAC	217325
rs222940827	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115826112	TCAGAGAAAAATAAA[C/T]AAAGGGAAGGCTCAA	217325
rs222958192	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115846308	TTAGCTCCAGCTCCC[A/T]CGGGGTCTGCTGCCT	217325
rs223115469	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115851666	AGCGGATGCAGAGGC[C/T]GTGGAGGGTGCTGCT	217325
rs223115600	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115845204	TGTTCCCTGCTGCCT[A/G]TAAAGTGGTTATGTC	217325
rs223157565	snp	C/T			missense, nc-transcript-variant	Llgl2	Mm_Celera	11:115843365	GCCCTTGGCTATAGC[C/T]CTTCGCTGCGCATCC	217325
rs223207519	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115849207	GTATGGCAGAGAATA[A/C]ACTTACCACCCCTCC	217325
rs223339405	snp	C/T			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	Mm_Celera	11:115822899	CACCCTCTTGCCTGG[C/T]CACTGTGCTTTCAAG	217325
rs223349435	snp	A/G			synonymous-codon, nc-transcript-variant	Llgl2	GRCm38.p3	11:115848276	CAACGGCCAGCAGAC[A/G]GCCTTCGACTTCACC	217325
rs223349737	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115839764	ACACTCAGGGGACTC[C/T]GAACCTTGAAAGTTT	217325
rs223360813	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115842653	CTGTCTGTAGCTCCT[C/T]GCACACCAACGGTGA	217325
rs223371724	snp	A/G			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823461	CCCCCTTGAACCTCA[A/G]GCTCCAGCGGCCCCT	217325
rs223489259	in-del	-/G			intron-variant	Llgl2	Mm_Celera	11:115837314	GTGAGTGTGTGTGGA[-/G]GGGGGGGGTGGATAA	217325
rs223623080	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115852415	AATCACATAGGCAGA[G/T]CTGCTGCCCAGGACC	217325
rs223636773	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115847896	GCCCAGTGTGGGGAC[A/G]GTTTAGGAGGCCACT	217325
rs223692293	snp	A/G			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823258	CAAGATTCCAATCTT[A/G]GTCCTGCCCTGAGGA	217325
rs223859091	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115826022	TGGAACTCAGGTCAT[A/C]AGGCTTGTCTCCAGG	217325
rs223872236	snp	A/G			missense, nc-transcript-variant	Llgl2	Mm_Celera	11:115844501	CCTTCCAGATATGGC[A/G]CCCCCGGGGTAGAGT	217325
rs223913483	in-del	-/TGCT			intron-variant	Llgl2	Mm_Celera	11:115828186	CCTGGACTGTCCCTC[-/TGCT]TGCTTAGTCATTGAT	217325
rs223960283	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115837057	GGTAACCCGGGTTTC[C/T]TTCTGTACATCATAG	217325
rs224256146	in-del	-/CTAA			intron-variant	Llgl2	Mm_Celera	11:115846452	GTCTCTCTAGACACT[-/CTAA]CTGTCTCAGACATTG	217325
rs224413448	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115838397	AGGTTTCATGGCTCT[A/G]TTTATTTTAGTTTGT	217325
rs224621606	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115842769	TGACCCCTCCGGGAT[A/G]TTCTCCAGCCATTTT	217325
rs224761772	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115834656	GGTGACCCTGGGCTT[A/G]GACAGCTGTAGGCCT	217325
rs225352395	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115842167	TGAACAGGGACTGGG[A/G]CTGGCTGGGGCCCTC	217325
rs225373506	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115838912	AGGCCTAGGTGCCTG[C/G]GCTGGACTGCTGCAG	217325
rs225484916	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115846325	GGGGTCTGCTGCCTT[A/G]GGCCTCTACTGACAG	217325
rs225516210	snp	C/T			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115844897	CCTGAAGGTCAAGGG[C/T]GGGGTGTCAGAGCTG	217325
rs225529727	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115838315	TTGATTAGCCTGTCT[A/G]TTCCTCAGTTTCCTC	217325
rs225552140	snp	C/G			intron-variant	Llgl2	GRCm38.p3	11:115845338	TTCCCCCTTCCTGGA[C/G]AGCAGATATCTCATC	217325
rs225557569	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115836617	TGGTCCCCAAATAAC[A/G]TGTGACCCCTGGATC	217325
rs225596487	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115843559	TGAGAATTTAGCACC[G/T]CGAGCTGTGTGTCCT	217325
rs225701898	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115837149	AGAATTGTCCTGGGC[A/G]CTGTAGTTAGCAGCA	217325
rs225766689	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115837999	CGCCACACGACAGAT[A/G]CCCAAACAGCTTACA	217325
rs225830836	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115841495	ATGTAAGGTGAGGCC[C/T]GAGGTTGGCCTCCCT	217325
rs225893434	in-del	-/TT			intron-variant	Llgl2	Mm_Celera	11:115827920	GACTAGAGCCCTCTC[-/TT]GAGGGACTTGGCTTG	217325
rs225919195	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115832640	CCTTCCCTAGAGTCC[G/T]CTGGTCTCTTTCCTT	217325
rs225921992	snp	C/G			downstream-variant-500B	Llgl2	Mm_Celera	11:115855903	GAGAACTCCCTCTTA[C/G]AGTATTTGAATCACC	217325
rs225961141	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115825800	TGGTCTACAGAATGA[A/G]TTCCAGGATATCCAA	217325
rs226001756	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115833254	TTGATTGATTACAGA[A/G]CTGAGGATGAAGGGC	217325
rs226214806	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115835869	TATGCCTTTTATTTG[A/G]GGCTTTGGTTTGGGC	217325
rs226239461	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115840395	AAGTAAGAGATGGGG[A/G]ATGCCCAACCTTTGC	217325
rs226263294	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115837109	ACCCTCCTCACTGGC[A/G]ATGTCTGGGGCCTGT	217325
rs226278080	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115832133	TGGAGTTAGTCATAC[A/T]TGGGGGTCAGCTCTG	217325
rs226492026	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115834101	CCCGACCTGGGTATT[C/T]CTGCTAAAACTGCCC	217325
rs226539752	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115830159	TCCTGCATCCAAAGA[C/G]TAATCCCACCACCAA	217325
rs226593272	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115838464	ATGGGCACCACATGC[A/G]TGGCTGGTGCTTCCA	217325
rs226725543	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115830623	GTCATTCCTCAGGTA[C/G]TGGCCACCTTGGGTT	217325
rs226759691	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115831069	GGCCCTGCCTCTGGC[C/T]GGCTGGCTTTTTCAT	217325
rs226775616	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115837779	ACACGTGTGTCCACC[A/G]AGTGCTTGGCTAAAC	217325
rs226923858	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115829530	GAAAGGCCAGGGTAG[A/G]GGGTGGGGGTGGGGC	217325
rs226963388	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115853180	AAACACAGAGGGCCC[A/G]ATCTTGGGCTAGGGA	217325
rs226967831	snp	A/C/G			intron-variant, nc-transcript-variant	Llgl2	Mm_Celera	11:115854955	CCAGAGGAAGCCAGG[A/C/G]ATGCTTTTTGTGGGC	217325
rs227007294	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115835639	CACCCAGCAATCTGG[A/G]GCCGCTTGGGGATAA	217325
rs227007752	snp	C/T			intron-variant, downstream-variant-500B	Llgl2	Mm_Celera	11:115855446	TACTGTCCTGACCTA[C/T]TGTCTGTGTCCTTCC	217325
rs227042546	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115827578	CTGCTCTCTCCCTCC[A/T]CCTGAGCCCGGGCAT	217325
rs227167690	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115828315	AGGACAGGAAATAAA[C/T]ATGGCTAATAATCAT	217325
rs227216020	in-del	-/AGG			intron-variant	Llgl2	GRCm38.p3	11:115848140	CCGCTTGTGACTATC[-/AGG]AGTTGTACAGGAGCC	217325
rs227227120	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115828082	TCTGAGTGGCCTTTG[C/T]CTGTGTCTTGAGAGC	217325
rs227328630	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115850606	TAGCCTCTGCTGAGC[A/T]ATCTGCCACCCCCAC	217325
rs227370659	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115852529	AGTATGGACTTACTT[A/G]GACACAGCACCTAAC	217325
rs227533250	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115847519	CCCCTCACAGGCTGA[C/T]TTGTGGTTACATTGG	217325
rs227641004	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115832328	ACCTGGTCCCCACAT[C/T]TTCCTGAGGTTCTCT	217325
rs227674024	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115837435	GAAGACAAGGTCTCA[G/T]TATGTAGCCTTGGCT	217325
rs227755130	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115834912	AACAAGGTAAGGATG[C/G]GGTGAGGGAGGGCAG	217325
rs227765602	in-del	-/A			intron-variant	Llgl2	Mm_Celera	11:115846182	TTACTTGCTTTCATT[-/A]AAAAAATGTCCTTTG	217325
rs227791061	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115829073	TTGGGCTGGGGCAGG[C/G]TGGGGGTGGGAGGGT	217325
rs227798445	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115852627	TTTTCCCTGCTGGCT[C/G]TGAGCGGTGTCTGCT	217325
rs227799800	in-del	-/CAG			intron-variant	Llgl2	Mm_Celera	11:115839201	CCCTCCTGAGGCCCT[-/CAG]CAGCTTCTGGGAGCT	217325
rs227802318	in-del	-/T			intron-variant	Llgl2	GRCm38.p3	11:115829588	GTCTTTCTTTAAGTC[-/T]TTTTTTTTTTCCAGG	217325
rs227822354	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115829749	TCCACACACAAAGCA[C/T]AGATCTGTGTGGAAA	217325
rs227824776	snp	C/T			upstream-variant-2KB, missense	Llgl2, Tsen54	Mm_Celera	11:115822620	CTCTGCAGCCTCAAG[C/T]GCTTGACCTACCAGA	217325
rs227939592	in-del	-/TGTGTGTGTGTGTGTGTA			intron-variant	Llgl2	Mm_Celera	11:115846743	GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGTGTA]TACACGTGCATGCAT	217325
rs227940293	snp	C/G			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823171	AACCCTGGTGGGCCA[C/G]AGAGCACATGGGAGA	217325
rs227980611	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115830516	AACTTTCATTTTATA[C/T]ATCTTTAGGTGTATG	217325
rs228017959	snp	C/T			upstream-variant-2KB	Llgl2	Mm_Celera	11:115823711	TTGTGCTTTCAAGTC[C/T]GCTGCCTGCATGGAG	217325
rs228092612	in-del	-/AT			intron-variant	Llgl2	Mm_Celera	11:115846379	CACAAGGGCACACAC[-/AT]GTGTACATGATTAAA	217325
rs228097519	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115830676	GACCTGGAACTCACC[G/T]TGCACAGTGAGCCAC	217325
rs228108110	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115851337	ATACTTATGTTAGAG[G/T]TAAGTCCCGAGCAAA	217325
rs228124799	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115831277	CGAGGTCCTGAGTAG[A/G]GGATACGAGGAGAAA	217325
rs228197738	in-del	-/T			intron-variant	Llgl2	Mm_Celera	11:115838751	CCACTGAAGACTAGC[-/T]TAAGGGAACAGGGAC	217325
rs228200859	snp	A/C			intron-variant	Llgl2	GRCm38.p3	11:115826457	AAAAAAAAAAAAAAA[A/C]CCGAGGGAATGGAAA	217325
rs228248584	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115826821	AGGGGACTTGCAAAA[C/T]CAGTGCTGTCTTGAT	217325
rs228452651	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115837954	GCGTGTCGTGGGCAA[G/T]GCGTGCAACAACAGA	217325
rs228505849	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115826914	GGTGTGGGAGGACAG[A/G]AGGGGTGCTGCCTCT	217325
rs228514321	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115829817	GACTATCTGCCCTTG[A/T]GGGATCTGAACCGGG	217325
rs228593054	in-del	-/AG			intron-variant	Llgl2	Mm_Celera	11:115830967	AAAGATTCTTCAGAC[-/AG]AGCAGTGGCAGCCAG	217325
rs228731539	snp	A/G			downstream-variant-500B	Llgl2	Mm_Celera	11:115856152	ATACAGAGGCACATG[A/G]CCTGGTGGGTGCAAG	217325
rs228872915	snp	C/G			intron-variant	Llgl2	GRCm38.p3	11:115848498	CTCCCAGGTGGAGAC[C/G]CAGTCTGGAAGGCCA	217325
rs229048613	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115827473	AGGCTGGAGAAGCTG[A/C]CTCTGCCTCTGCAAG	217325
rs229063764	snp	A/G			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115822390	TTACTGGCTAAGAGT[A/G]GTTAAGAACCCACAC	217325
rs229192578	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115851344	TGTTAGAGTTAAGTC[C/T]CGAGCAAATATGCAC	217325
rs229218697	snp	A/G			intron-variant, nc-transcript-variant	Llgl2	Mm_Celera	11:115854670	GCTGAGGGTGAGTGA[A/G]AGGCAAGATAGTCTG	217325
rs229310615	in-del	-/AGG			intron-variant	Llgl2	Mm_Celera	11:115829566	ATAAGAGAGAGAGAA[-/AGG]AGGAGTCTTTCTTTA	217325
rs229330646	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115826170	TGCTGTGTGGCTCAC[A/G]CCTGTAATCCCAGCA	217325
rs229371718	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115849388	TGGCACTTCAGCTTA[C/T]TGCTCTTATTTTGCA	217325
rs229439605	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115843737	CCACAGCAGGGGGTG[A/T]CTGGGATACAGGTGG	217325
rs229462315	in-del	-/A			intron-variant	Llgl2	Mm_Celera	11:115830408	GGTGGGGGTGGGGGG[-/A]GTCCTTGTCACTGGT	217325
rs229658052	snp	C/G			intron-variant, downstream-variant-500B	Llgl2	GRCm38.p3	11:115855429	CACCTTCCCTGCCCA[C/G]CTACTGTCCTGACCT	217325
rs229692412	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115846288	TCAGGTGGCTCACAG[C/T]CATCTTAGCTCCAGC	217325
rs229703638	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115849319	CTCCGGGCCTCTTGT[C/T]AGGCTCTGAGGGGCA	217325
rs229726951	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115846824	CCATGTCTTGTTCTA[C/T]ATGACCCTCACTGTG	217325
rs229730491	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115838124	GTTACCTGTCCTTGG[A/C]CAGGAGTTGTGACCA	217325
rs229766827	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115838689	GCTGTCTACCACTTG[G/T]ACCCTCTTAGCACAC	217325
rs229767871	snp	A/T			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115822444	CTCCTGAAGCACTCA[A/T]CCAAGCCATGGAGTT	217325
rs229880108	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115852438	CCAGGACCCTCAGAG[C/T]GGTACTCATTCAGTT	217325
rs229928670	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115846525	CCTGCCTCTGCCTCC[C/T]AGTGCTGGGATCAAA	217325
rs230002156	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115852067	CCCTTAGCATTGATC[A/G]AGTGAGTGTCCTGAG	217325
rs230119421	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115850204	AAGCTAGGATGCGCC[C/G]TGGCCACTCACAGGC	217325
rs230136129	in-del	-/TG			intron-variant	Llgl2	Mm_Celera	11:115846781	GTGCATGCATATGTT[-/TG]TGTGTGTGTGTGTTA	217325
rs230146104	snp	G/T			upstream-variant-2KB, synonymous-codon, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115822065	TGACGCTGTGGCGAC[G/T]TTCCGAAAAAACAGC	217325
rs230269352	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115833841	CTCACTTTGTACCCT[C/T]CATGGCTTTAAACCC	217325
rs230343805	snp	A/G/T			intron-variant	Llgl2	GRCm38.p3	11:115845797	CGGATTTCTGAGTTC[A/G/T]AGGCCAGCCTGGTCT	217325
rs230389431	in-del	-/AGGCAACC			intron-variant	Llgl2	Mm_Celera	11:115827411	CTTCCTAGTTTTCTA[-/AGGCAACC]AGGAGCAGCTGCTGA	217325
rs230405074	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115850580	CTGAGTCCTTTGCTG[A/G]CCGGGCTGTCTAGCC	217325
rs230480840	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115828392	AGGGCAGGATGTGCC[A/G]CAATGGATAGAACTG	217325
rs230560971	in-del	-/TC			intron-variant	Llgl2	Mm_Celera	11:115851534	CCAGAAAGTCTGGTG[-/TC]TTAGTCAGGGTTTCT	217325
rs230714198	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115840654	CTGTGAGTTTGAGGC[C/T]AGCTTGCTTGGTCTA	217325
rs230714886	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115828800	CACTGCTCGAACATT[C/G]TGAGTAGCTGAAAGT	217325
rs230732595	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115847748	GAGGACACAAGGATC[G/T]TGGTCCCGGGTTGGG	217325
rs230990639	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115841813	GTGAGCCTTGGCCGC[G/T]TGACTGCTGTCCTAG	217325
rs231058538	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115840137	TAAGATGCCCTGGGG[A/G]CGGGGGCACACTGCA	217325
rs231111716	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115841305	AATCTAACACAGATC[C/G]TCTGGGAGAGGAGTC	217325
rs231428349	snp	C/G			upstream-variant-2KB	Llgl2	Mm_Celera	11:115823952	GATGCGCTCCTGCCC[C/G]GTCGGCTCGGCCTAG	217325
rs231441895	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115843292	GACTCGCCTATAGGC[C/T]CAGCCCACATGCTTC	217325
rs231470264	in-del	-/TAC			intron-variant	Llgl2	GRCm38.p3	11:115826440	GCCCCAAGACCCTTT[-/TAC]AAAAAAAAAAAAAAA	217325
rs231493924	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115836934	CGGAGTACTTGAGAC[C/T]CTGAAGAGTCTTATC	217325
rs231558663	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115843789	CTGGGACAACTTCTC[C/T]GAAGTCCTGGACAAC	217325
rs231563823	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115835229	GTCTCTCCCTGGCTA[C/G]AAATGACTGAGAGTT	217325
rs231579346	in-del	-/TTTTTTTTTGTTTTT			intron-variant	Llgl2	GRCm38.p3	11:115851432	TGTGGAGGAGAGGGG[-/TTTTTTTTTGTTTTT]TTTTTTTTTTTTGGT	217325
rs231592423	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115835774	GGTGCAATTCTGACA[C/T]TTTTGGTACTGAGGA	217325
rs231613067	in-del	-/ACTA			intron-variant	Llgl2	Mm_Celera	11:115830069	TCTAACCAGCGGACT[-/ACTA]ACTAAGCACTCCCAA	217325
rs231731832	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115829203	GCTGGGCATGGCTCC[A/C]GCACCTCCTGTCCCT	217325
rs231922431	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115830820	CTTTGAAGGTCAAGC[C/T]CGGGTCCTCATGCTT	217325
rs231923812	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115839892	CACCCAGGCTTCCTA[A/G]TTCCTCCTTGTTTCC	217325
rs231986508	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115842861	CATGTCCATGAACAC[G/T]CGGGGAAGTGTTCAT	217325
rs232114159	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115853488	CCAGCAGTGTTCAGC[C/T]CCTGGGTGGATACAA	217325
rs232371764	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115839702	GAAAGGCCACCTCAC[C/T]CTTTAGGGACCTAAC	217325
rs232602509	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115837912	TCACATCTGGGAGTG[A/C]CACCCTGAAGGTCAG	217325
rs232621624	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115843673	TATACTTGATTGTAG[A/G]GCCCTGGGTGACTAC	217325
rs232815514	in-del	-/GGCTTCGGCCGGCCAGAGCT			intron-variant	Llgl2	Mm_Celera	11:115841922	ATTCTACATTCCAAA[-/GGCTTCGGCCGGCCAGAGCT]GCCACTGCTGGTGGT	217325
rs232833679	in-del	-/TATGCTAGAGA			intron-variant	Llgl2	Mm_Celera	11:115830456	ATTCTCCTGATAGCT[-/TATGCTAGAGA]AAGGCTAGAGAAGGA	217325
rs232884974	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115829917	CCATCTTTAGAAGCT[A/G]GGGTGGAGAAGCCCA	217325
rs232901821	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115841996	TCTCTATCTCTTCTC[A/C]AGGCTTCAGTAACCT	217325
rs232934935	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115833808	AAGGCCTCCTTAGGG[A/G]GTGGCAGGAAATAGG	217325
rs233036852	in-del	-/TGT			intron-variant	Llgl2	Mm_Celera	11:115843462	GGCCAAGGTGATCTC[-/TGT]TATGTGTATGTGGGG	217325
rs233049986	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115838528	TGGCTGTGTCCCATC[A/G]TGTGGGTGCTGGAAC	217325
rs233156137	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115831250	CCTTATGTGGCCGGT[A/C]ATACCTGTCACCGAG	217325
rs233301984	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115845569	GTGTGGGCCACGGCC[C/T]TCTCCTGGGCCCCAG	217325
rs233320748	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115851550	TTAGTCAGGGTTTCT[A/T]CTGTTGTGATGAACA	217325
rs233353122	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115837280	CTCCTCTGAGAATGT[C/T]TAGAATGGGAGGGTG	217325
rs233390001	snp	C/T			downstream-variant-500B	Llgl2	Mm_Celera	11:115855897	GGTTCAGAGAACTCC[C/T]TCTTAGAGTATTTGA	217325
rs233563728	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115828660	AGTCAAGCTGCCTAG[C/T]TGTCTCTGGCACACT	217325
rs233582871	snp	A/G			downstream-variant-500B	Llgl2	Mm_Celera	11:115856247	AGTTTAGCTCTGGCT[A/G]TCCTAGGACTCGCTC	217325
rs233625888	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115841144	GTTTATTTTTTTATT[G/T]TTTGTTTTTATTTTT	217325
rs233723046	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115827941	GACTTGGCTTGGTAT[G/T]CTCAGGGTAAATAGT	217325
rs233756213	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115828404	GCCACAATGGATAGA[A/G]CTGGATGCCGCTGTA	217325
rs233792974	snp	A/G			intron-variant, nc-transcript-variant	Llgl2	Mm_Celera	11:115832732	GAGCGCCTGCACCCC[A/G]GGAGCCGTAGCTGCT	217325
rs233813051	snp	C/T			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115849637	CTTGCACTGTTCCGC[C/T]ATCACCTGCTCCCAC	217325
rs233874903	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115834395	TAGAGCATCAACCAC[G/T]GGGAGAGACAGGCCC	217325
rs233893040	in-del	-/TGTGTGTGTGTGTGTGTGTGTA			intron-variant	Llgl2	Mm_Celera	11:115846739	GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGTGTGTGTA]TACACGTGCATGCAT	217325
rs233914717	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115851002	ACGACATTCCACTTC[C/T]TCAAGGTGCACACTT	217325
rs233989463	snp	A/G			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	Llgl2	Mm_Celera	11:115855493	GACAGCACCCAGGCT[A/G]TGGGATGATCACACA	217325
rs234081407	snp	G/T			intron-variant, splice-donor-variant	Llgl2	Mm_Celera	11:115825254	AACAAATGAGTCAGG[G/T]AATTTTCTTTTCTCT	217325
rs234214534	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115833231	TAAGCAAAGTCTTGG[A/C]CCTTTAATTGATTGA	217325
rs234260778	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115827702	TACTACCTGCCCTCG[A/C]CAGTCTCTGATCCGT	217325
rs234392408	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115826540	GGATTCCTTTGCCTG[C/T]CGTCTTTTCTTCACA	217325
rs234511205	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115830759	TCTCTCAGCCTCTGC[C/G]CGGAGGTTACAGGCA	217325
rs234561184	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115828351	TGCAAATGACACCAG[C/T]TATAGGGTTGGGAGA	217325
rs234607108	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115829342	TGGGCAGATGGGCCC[C/G]GCTTGGCTACACCTT	217325
rs234647485	snp	A/T			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115824252	TCGGCTCGGGAGGAT[A/T]CGAGTCCCCTGGGTT	217325
rs234743103	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115830096	CCAACTTTTGCACCT[A/G]TATCGGGTGGCGTCC	217325
rs235239803	in-del	-/CGGGAAAGC			intron-variant	Llgl2	Mm_Celera	11:115826977	AGTTCACTTATTCCT[-/CGGGAAAGC]CGGGAAAGCCGGGGT	217325
rs235307610	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115849092	TCATCTCTTCCTTGA[C/T]AAGCAGTTCACATGC	217325
rs235369342	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115843215	CTCAGAGCCCCCTTT[C/T]CCTGATTGAGCTGTG	217325
rs235415266	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115849162	CGCTGCCTCACCTTG[C/G]TTTAGGCCTACCAGG	217325
rs235565492	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115853454	CACGTGACAGGGTCC[C/T]CTGGATGTCCCTAAG	217325
rs235740804	in-del	-/G			intron-variant	Llgl2	Mm_Celera	11:115831320	GGACAGTTGTAGACT[-/G]GGGCGAGGGAGCATT	217325
rs235780968	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115836517	TCAGCAAAGGGATAA[A/G]CCTTGGTTCCTGTGT	217325
rs235806257	in-del	-/GT			intron-variant	Llgl2	Mm_Celera	11:115846719	GGCACCTGAGTTTGC[-/GT]GTGTGTGTGTGTGTG	217325
rs235817702	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115833073	TTTTGATTGTCCCCA[A/G]AGGGTGACAGTTCCC	217325
rs235859637	in-del	-/TT			intron-variant	Llgl2	GRCm38.p3	11:115850393	GGTTGGGTGGTTTGG[-/TT]GGGGGGAGACGGGAA	217325
rs235885181	snp	C/T			synonymous-codon, nc-transcript-variant	Llgl2	GRCm38.p3	11:115847200	CAGCTGGCAGCGGGA[C/T]GGCTGCCTGATTGTC	217325
rs235980869	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115851396	ACTGTTGCTGAGATG[C/G]AACACTGTGCCCAAA	217325
rs236017795	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115845743	GCTAGTTGTGGTGAC[A/G]CTCGCCTTTAATGCC	217325
rs236032141	snp	G/T			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823525	ACCGGTTGGGGGTTC[G/T]CCATTACGTTTTCGT	217325
rs236085528	in-del	-/C			intron-variant	Llgl2	Mm_Celera	11:115836990	AGGGGAATGCTGTAT[-/C]CCCCGAGGGGCTTTG	217325
rs236146536	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115850499	CCCAGAGTGATGACT[A/G]TTCCGCCTCCAGAAA	217325
rs236226747	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115845231	TGTCATAGCTTGAGC[A/G]AGATGCTCTGAAGCC	217325
rs236279011	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115828518	CCCAAAGTGTGGCCC[C/T]GGGGATACAACTGGA	217325
rs236304007	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115844275	CCCAACCCCCCCCCC[A/C]CACACACACACCCGT	217325
rs236307166	snp	A/G			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115850680	TGCTGTGGAGCAGGT[A/G]GAGGCTGACCTGCTG	217325
rs236394557	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115827289	GAGAAAAAGGAGTAT[A/G]GGGGAAATTTGGAGT	217325
rs236610733	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115840528	GACTTCCCTGAGGAT[A/G]CGAAGTCAGAATATT	217325
rs236625469	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115826570	ACAGTACCTCACTCA[C/T]CCCAGGCATCAGATG	217325
rs236648141	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115841681	TGACTTTCATGCCTT[C/T]GCTCCCCCTGAGTGC	217325
rs236677965	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115851667	GCGGATGCAGAGGCT[A/G]TGGAGGGTGCTGCTT	217325
rs236682976	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115833457	TCTACCTGACCCTAC[A/G]TGCAGCGTTCAGCGA	217325
rs236684867	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115842617	CAATGCTTTGACATC[A/G]GCTGTTGGCATTCGC	217325
rs236691713	in-del	-/GGCG			intron-variant	Llgl2	GRCm38.p3	11:115835474	TCCAGCCTGGGAGGA[-/GGCG]GGGGGGGGGGGAAGA	217325
rs236777576	in-del	-/TTCTGT			intron-variant	Llgl2	Mm_Celera	11:115827106	CTGTCTGTCTGTGTC[-/TTCTGT]TTCTGTTCTCCACCC	217325
rs236833393	snp	C/T			intron-variant, nc-transcript-variant	Llgl2	Mm_Celera	11:115825210	CAGTGCAAAGACCGG[C/T]AGGAGGACAGTGGAG	217325
rs236954466	snp	A/T			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115822395	GGCTAAGAGTAGTTA[A/T]GAACCCACACCTCCT	217325
rs237074234	snp	A/G			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823299	GGTGGTGGTAGGAGG[A/G]TGGCTGAGAGTCCTG	217325
rs237217305	snp	C/T			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	Llgl2	Mm_Celera	11:115855622	CCGGGGCCGCCCCTC[C/T]TGGGCCCTGTCTGTC	217325
rs237244153	in-del	-/TG			intron-variant	Llgl2	GRCm38.p3	11:115827061	CTCTTCCCCTCTCCC[-/TG]TGTGTGTGTGTGTGT	217325
rs237269800	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115849467	TTGTCTACAGGCCAG[A/T]CGGGACTGGCTGCCT	217325
rs237382377	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115852670	AGGCAGAGCTGTCCT[A/C]GGTTTAGGATCACCT	217325
rs237434949	snp	C/T			synonymous-codon, nc-transcript-variant	Llgl2	GRCm38.p3	11:115847026	CTACAGCCGAGGCCT[C/T]GTCGTCATCTGGGAC	217325
rs237502440	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115848535	CAGGCCACACCTTTT[A/G]CCTGTCCCAATCCCT	217325
rs237609567	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115834184	GACAGCCCCGCTTCT[A/G]CCAACCCACTGCACG	217325
rs237753787	snp	C/T			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115850839	CTTGGCTCTGCACTC[C/T]GAGTGGCGGCTTGTG	217325
rs237800247	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115845080	GTGTTCAGGCTACCA[C/T]CATCTCGTGCTCTGG	217325
rs237829443	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115843496	GTGAGATCTGGAGAG[A/G]GCCAGTCTTACCCTG	217325
rs238010651	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115830386	TGCAGGTCTGAGCCC[C/T]TTCACGGGGTGGGGG	217325
rs238031731	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115848615	GCCAGTCCAGCTTAG[C/T]GAGAGGGTCCTGGCT	217325
rs238067492	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115841358	CCAGTCCCTAATTTG[C/T]TTTGTTTTGTTGATA	217325
rs238114608	in-del	-/CC			intron-variant	Llgl2	GRCm38.p3	11:115843627	ACTCACGTCCCCGTT[-/CC]CCCCCCCCCCGTCCC	217325
rs238183210	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115846413	CAATAAAATTATCCT[C/T]TGAGGGGAGTGGGTT	217325
rs238220061	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115838417	TTTTAGTTTGTTTCC[A/T]ATATGTATGCATGTT	217325
rs238249628	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115839213	CCTCAGCAGCTTCTG[A/G]GAGCTCTCCTCTCAG	217325
rs238268761	in-del	-/GAC			intron-variant, nc-transcript-variant	Llgl2	GRCm38.p3	11:115854954	CCAGAGGAAGCCAGG[-/GAC]AATGCTTTTTGTGGG	217325
rs238286420	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115852483	CAGAGCCAGCACCTG[C/G]CTTGATAGCCTTGCT	217325
rs238381290	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115827831	AGAATTCTTGAGCTA[C/G]GAGAGGCTCCTTTGG	217325
rs238465999	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115846216	TAGGCAGATGGCTCC[A/G]TAGTTAAGTACTTTC	217325
rs238508118	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115838049	GTTCTAGGCCTTTCC[A/C]CAGAGCCAGCAAGAT	217325
rs238569761	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115843650	CCCCGTCCCCCCCCC[C/T]TGACTTGTATACTTG	217325
rs238638041	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115836011	TTTTCTGCTTATGAA[C/T]GAACCAGGAGAGTGT	217325
rs238743221	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115837854	GGAATTCCTCATGTG[C/T]AGGTTAGGGTCCGCG	217325
rs238774231	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115838238	TGGTTGGGGCAGGGA[A/T]CTGGAGCCATATAGC	217325
rs238779657	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115829726	CCAGAGGTGGCTCTC[A/T]GGCTGGTTCCACACA	217325
rs238825607	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115828602	CGTGTTTAAGGACTG[C/G]TAGGAGACCCTAGGA	217325
rs238836440	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115836724	CTGATCCGTACAGTC[C/T]AAGGCCTGGCTCTGT	217325
rs238851334	snp	C/T			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115824498	GGGGGACACAGTGAG[C/T]AGAGACACCGTTCCC	217325
rs238871618	in-del	-/C			intron-variant	Llgl2	Mm_Celera	11:115831455	CCCACCCCCACCCCA[-/C]CCCCAGCGCCCTTGA	217325
rs239019015	snp	A/G			downstream-variant-500B	Llgl2	Mm_Celera	11:115856071	TCCTAGTAGAACACA[A/G]GTGAGGGGTAACCTC	217325
rs239032586	snp	A/T			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	Mm_Celera	11:115822813	TCTCTCATATAGGAC[A/T]CACCTGGATGGAACC	217325
rs239122235	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115831432	CCAGTAACTCTCAGC[A/G]AGGCTTCCCCACCCC	217325
rs239181827	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115834390	GGCATTAGAGCATCA[A/G]CCACGGGGAGAGACA	217325
rs239220625	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115835401	TGATGTTGCAGCCCT[G/T]TGGCCTCAAGGACCA	217325
rs239220680	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115826779	TTAGCCCCATTGAAG[C/T]CTTTTAGGTAGACAC	217325
rs239270294	in-del	-/A			intron-variant	Llgl2	Mm_Celera	11:115826521	CGAGAAGCAAGGCAG[-/A]AGGGGATTCCTTTGC	217325
rs239412339	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115846312	CTCCAGCTCCCACGG[A/G]GTCTGCTGCCTTGGG	217325
rs239643365	in-del	-/TATCCGGAGC			intron-variant	Llgl2	Mm_Celera	11:115839545	TCCACCTTCTTGTTT[-/TATCCGGAGC]TAGAGTTCTCTGGGG	217325
rs239681463	in-del	-/GGGG			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115824872	GCTTTTGCTCGGTTT[-/GGGG]GGGGGGGGGGGTTGG	217325
rs239899618	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115840057	TGTCCAGGGAAAGTC[A/C]TGGGAGCCTATGTCC	217325
rs239953406	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115844035	TCAACCTTACCCCAG[C/T]GGTTAATCATTACCA	217325
rs239957352	in-del	-/TTTTTT			intron-variant	Llgl2	Mm_Celera	11:115841393	GTCTCTAAATTCTGA[-/TTTTTT]TTTTTTTTTTACACT	217325
rs240054812	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115827375	GACAGACAGACCCTC[C/T]GACCTTGTGGGGAGC	217325
rs240203402	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115849050	CTCCCCTCTTATTGC[G/T]CCGGCTACCTAGAGC	217325
rs240252116	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115842393	TTTCTCCTGCTGTCG[C/T]CAGGGCTTATCTCTC	217325
rs240275220	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115835873	CCTTTTATTTGGGGC[C/T]TTGGTTTGGGCTTCC	217325
rs240346991	snp	C/G			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115850032	GTTCTGGGACGCCTC[C/G]GGTGTGTGCTTACGT	217325
rs240384001	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115850442	GTCAGGAGCACAACC[G/T]CTGCTTTTCCTAGCA	217325
rs240469757	snp	C/T			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115824563	GGCGACCCGGCTTCC[C/T]GTGACCCGGCGTCGC	217325
rs240481075	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115842572	GTAGGGTAGGTAGCT[A/G]TTGGGAAGCAGAAGC	217325
rs240515252	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115834140	TCCCCTGCATGTCCA[A/G]TTGAGGCACCGATCA	217325
rs240662878	in-del	-/A			intron-variant	Llgl2	Mm_Celera	11:115836822	CTTTGTCTAGGGGGT[-/A]AATGGGAGGGAGGAG	217325
rs240671601	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115831210	CATGCTCTTCCACCC[A/G]CCTGACCCTTAGCCC	217325
rs240680226	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115845776	CACTTGGGAGGCAGA[C/G]ATAGGCGGATTTCTG	217325
rs240710995	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115852984	GCTGGCCCCACTCAA[C/T]CCCCAGGGTTGGGGG	217325
rs240742858	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115837747	GTAAACAGAGCCAGC[A/G]TGACGTGAAGGGCTG	217325
rs240746219	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115847524	CACAGGCTGACTTGT[A/G]GTTACATTGGAATAA	217325
rs240893892	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115829626	CAAGGGGTGGACCAG[A/G]CTTATATGGGCCCAG	217325
rs241093221	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115828630	GGATGAGGTTGGCCT[A/G]GGACCAGGTAACTCA	217325
rs241118639	snp	C/T			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115822324	AAGTCTTTTTCCTCT[C/T]TCACCTAAGTCCTGG	217325
rs241188045	snp	A/T			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823560	ATACCACTTTACTAG[A/T]GGGTCTGAAACCTGA	217325
rs241455365	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115846052	GCATCTCTGGGCACC[A/G]CACACACATGCTAAA	217325
rs241588383	snp	C/T			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115851113	TCGGATGCGTCGCAG[C/T]AGAGTGTCCAGTCAT	217325
rs241626093	in-del	-/GGA			intron-variant	Llgl2	Mm_Celera	11:115835484	GGAGGAGGGGGGGGG[-/GGA]AGAGCACCTGAGGGA	217325
rs241812479	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115845900	aaacaaaaacaaaaa[A/C]aaaaacaaaaCTGAA	217325
rs242067604	snp	C/T			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115855085	AAAGGAAATCCAGAG[C/T]ACGCTGGAGGGGGAC	217325
rs242105791	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115851880	TCCTCTCAGATGACG[G/T]TCACCTGTGTCAAGG	217325
rs242142390	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115852345	ATGGCGTGAGGCCAC[A/G]GAGAGATGGGCTCTC	217325
rs242145179	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115846066	CACACACACATGCTA[A/T]ACTCATATACATAAA	217325
rs242182024	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115846340	GGGCCTCTACTGACA[C/G]TGACACTCATGTGCA	217325
rs242414269	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115849406	CTCTTATTTTGCACA[C/T]GGCAAGCAGTGCAGA	217325
rs242448805	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115850158	CCGCAAGGTGAGGCC[A/G]GGAGCCTGGGAGTCA	217325
rs242485292	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115843767	GTTTCAGCAGGGAGG[C/T]TCCACCCTGGGACAA	217325
rs242491046	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115849273	GGAAGAATTTCCCAG[C/T]GGCTTGTAGCTGCTC	217325
rs242526194	snp	A/G			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115849700	ACGCATCATCGCCGC[A/G]GGCAGCCGCCAGAAC	217325
rs242526376	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115842663	CTCCTTGCACACCAA[C/T]GGTGAAAAAGGCCCA	217325
rs242562991	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115843592	GAGCACAGAATGGGT[A/T]TATCTTCTCTTCTCT	217325
rs242701781	in-del	-/TTCGCCATTACGTT			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823522	GTAACCGGTTGGGGG[-/TTCGCCATTACGTT]TTCGTTCCCATACCA	217325
rs242787976	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115846894	GGTCCCCACTGTTGC[A/G]TGAGTTCATGGCACT	217325
rs242792665	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115850424	CCCCTGCCCGAGGGC[A/G]TCGTCAGGAGCACAA	217325
rs242833160	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115844364	ACTGCTATCCACCCC[C/G]ACCCTGTGCCCCTGA	217325
rs242865598	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115839776	CTCCGAACCTTGAAA[A/G]TTTACAAGAGTCTTA	217325
rs242933398	in-del	-/G			intron-variant	Llgl2	Mm_Celera	11:115831724	GCCTGGGGTGGGGGA[-/G]GGGGCTTTCTGAACT	217325
rs243027431	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115832381	ATTTGATGTTTCTAC[A/T]GTGAGCCTAGACAAC	217325
rs243046155	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115836858	TGCACCAATTGAGAC[C/G]TCAAGGTTCTGAGGG	217325
rs243115962	in-del	-/GGCTCTCCCA			intron-variant	Llgl2	GRCm38.p3	11:115847104	GCTGTCTGGAAGGGC[-/GGCTCTCCCA]GGCCCATGTGCAGAC	217325
rs243138308	snp	A/G			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115822198	CCAGACCCTGAAATG[A/G]GTCTGAGGTGCAGAA	217325
rs243178893	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115826189	GTAATCCCAGCACTC[A/C]TAGGACTGAGGTGGG	217325
rs243316564	in-del	-/TTTAAGCA			intron-variant	Llgl2	Mm_Celera	11:115830887	CTAAAATGTGATCAC[-/TTTAAGCA]TTTACGACCAGGACG	217325
rs243337422	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115835070	TTATTTCTGAGACGG[G/T]GATCTCACCATGTAG	217325
rs243503442	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115837509	AGATCTACTTGCCTC[C/T]ACCTAACGCCAACCC	217325
rs243514236	snp	A/C/T			intron-variant, downstream-variant-500B	Llgl2	Mm_Celera	11:115855431	CCTTCCCTGCCCACC[A/C/T]ACTGTCCTGACCTAC	217325
rs243845512	snp	C/T			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823556	TCCCATACCACTTTA[C/T]TAGTGGGTCTGAAAC	217325
rs243932801	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115851984	AGGCAAGTTCTCCTC[A/G]GGGAATCTCTTACTT	217325
rs243982020	in-del	-/CTCTCC			intron-variant	Llgl2	GRCm38.p3	11:115827017	AGACTCACTCTCACT[-/CTCTCC]CTCTCCCTCTCCCTC	217325
rs244099637	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115847466	TGGTTTTCTGGTACC[C/T]GCTGTGACTGCCTCA	217325
rs244332604	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115851753	CCAGCCTAGGGGATG[A/G]CACCACCCACAGTGG	217325
rs244391429	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115837981	CAGAACAGTGGCATC[A/G]CCCGCCACACGACAG	217325
rs244504406	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115837116	TCACTGGCGATGTCT[A/G]GGGCCTGTTGTGCTG	217325
rs244509142	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115845977	GACCCAGGTTCAGTT[C/T]CAAGCACCCACATGG	217325
rs244639173	in-del	-/T			intron-variant	Llgl2	Mm_Celera	11:115843618	CTCTGGTTACTCACG[-/T]TCCCCGTTCCCCCCC	217325
rs244716594	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115836698	CTGGTTCTCCTACTC[C/T]ACCTTAACCCCTGAT	217325
rs244732648	in-del	-/CC			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823444	CTATAGGGGCTGACA[-/CC]ACCCCCTTGAACCTC	217325
rs244737672	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115834672	GACAGCTGTAGGCCT[A/G]GGTGATCCTGGGCCT	217325
rs244842262	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115837229	CACAAAATGTCTCCA[A/G]CCATTGTCAGTTGAC	217325
rs244842410	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115828399	GATGTGCCACAATGG[A/G]TAGAACTGGATGCCG	217325
rs244876715	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115829005	GCAGGGGTGGTCTCA[C/T]ATCCGCCACTCAGGA	217325
rs244925060	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115841840	CTAGGCTGCTCAGGG[A/G]GTGGGGCCTCCTACT	217325
rs244934300	snp	A/G			downstream-variant-500B	Llgl2	Mm_Celera	11:115856174	GGGTGCAAGCAATTA[A/G]GGCATAGTTGGTAGC	217325
rs245197167	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115825803	TCTACAGAATGAGTT[C/T]CAGGATATCCAATGC	217325
rs245245611	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115830531	CATCTTTAGGTGTAT[A/G]TGCATGTTCATGCCT	217325
rs245256741	in-del	-/T			intron-variant	Llgl2	Mm_Celera	11:115839646	GGGGACAGGACACTC[-/T]TCTTGGCGGCTCCAC	217325
rs245348236	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115842770	GACCCCTCCGGGATG[C/T]TCTCCAGCCATTTTC	217325
rs245353599	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115833869	CCCTTGATGCTCTGT[C/T]TCCCCAGTGACCTAG	217325
rs245406423	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115839589	TGCTTGGGGTATCCC[C/G]AGGCTCTACCTGCTG	217325
rs245452623	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115831779	TCCTCCTCTAAGAAG[A/G]GGTGGGGTATTTTCA	217325
rs245492604	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115825296	TTTGTTTGTTTGTTT[A/G]TTGGTTGGTTGATTC	217325
rs245535302	in-del	-/TGAGGCCACGGAGAGATGGGCTCTCTGCCA			intron-variant	Llgl2	Mm_Celera	11:115852336	GAGACACTCATGGCG[lengthTooLong]TGAGGAAGTGGGCGG	217325
rs245680799	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115838031	ATCCCAGCTTCTAAA[A/C]CAGTTCTAGGCCTTT	217325
rs245702186	in-del	-/T			intron-variant	Llgl2	Mm_Celera	11:115836062	GGGCTTGTATACAGA[-/T]TGTCTCCTGCAACAG	217325
rs245758309	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115828157	TGACTAGAGAAGACC[A/G]TGCCTAGCTAATCCC	217325
rs246005334	in-del	-/C			intron-variant	Llgl2	Mm_Celera	11:115837172	AGCAGCACCCTAGTT[-/C]TGGCCAGATGCCAGT	217325
rs246020132	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115845182	CTTTCCCTTGCCTCC[C/T]AGTTCATGTTCCCTG	217325
rs246068523	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115837080	CATCATAGAATGCCT[A/G]AGCAGGGTTTCTCAC	217325
rs246107311	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115849053	CCCTCTTATTGCGCC[A/G]GCTACCTAGAGCTAC	217325
rs246155315	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115826644	CTCACTTAGCCACTC[C/T]GGGCCTGGGTTTCCC	217325
rs246226637	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115849381	TTGGTCGTGGCACTT[C/G]AGCTTATTGCTCTTA	217325
rs246279251	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115826542	ATTCCTTTGCCTGTC[A/G]TCTTTTCTTCACACA	217325
rs246345092	in-del	-/TTTTT			intron-variant	Llgl2	Mm_Celera	11:115834237	TTCTGGATTTTTATG[-/TTTTT]TTTTTTTTTTTCTTT	217325
rs246356393	snp	A/G			downstream-variant-500B	Llgl2	Mm_Celera	11:115855950	CCAGGAGTAGGGGTG[A/G]CTATGCAGCGTCTGT	217325
rs246461590	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115846243	TTTCTACTCTTGAAG[A/T]ACACTAGACTTCACT	217325
rs246462381	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115852531	TATGGACTTACTTGG[A/G]CACAGCACCTAACCT	217325
rs246606782	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115830664	GGATCTCTCACTGAC[C/T]TGGAACTCACCTTGC	217325
rs246828828	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115853188	AGGGCCCGATCTTGG[A/G]CTAGGGAGTGTGGTG	217325
rs246994263	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115829806	CCCTGAGTCCTGACT[A/G]TCTGCCCTTGAGGGA	217325
rs246995751	snp	C/T			upstream-variant-2KB, synonymous-codon	Llgl2, Tsen54	Mm_Celera	11:115822650	AGTGGGGATGTTCCC[C/T]TGATCTTTGCTCTAG	217325
rs247006400	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115827649	TAGAGTTTAGGCAGG[A/G]GATAGGAGAGGAGAT	217325
rs247030030	snp	C/T			missense, intron-variant	Llgl2	Mm_Celera	11:115851208	ACCATACAGCTCTCC[C/T]TCAGGATCTGAATCC	217325
rs247032842	snp	A/G			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823196	GGGAGAGCATGCCCA[A/G]GGCTGTGATCATGGA	217325
rs247064402	in-del	-/CCT			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	GRCm38.p3	11:115822405	AGTTAAGAACCCACA[-/CCT]CCTATCCCTCTACTC	217325
rs247079317	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115845370	GCAGCTGTCCCTGTC[A/G]CAGGGCTGCCCCCAG	217325
rs247186657	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115850621	TATCTGCCACCCCCA[C/T]CTCAGGTGCTGGTGC	217325
rs247428651	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115840456	CTGCTTAAGAGCTGA[C/T]GGGGCAGGTCGTGGC	217325
rs247451345	in-del	-/CCC			intron-variant	Llgl2	Mm_Celera	11:115829598	AGTCTTTTTTTTTTT[-/CCC]CCAGGAAGGTGTCAA	217325
rs247534044	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115849216	AGAATACACTTACCA[C/T]CCCTCCCTTGACATC	217325
rs247614381	in-del	-/A			intron-variant	Llgl2	Mm_Celera	11:115829687	GCTGATAGTGGTAAG[-/A]AAAGGAAATGACCAA	217325
rs247621469	snp	C/G			intron-variant	Llgl2	GRCm38.p3	11:115827075	CCTGTGTGTGTGTGT[C/G]TGTGTGTCTGTCTGT	217325
rs247629170	in-del	-/A			intron-variant	Llgl2	Mm_Celera	11:115829367	ACCTTGTTTGCATGG[-/A]GGACAGATTAGCTCA	217325
rs247675045	in-del	-/G			intron-variant	Llgl2	Mm_Celera	11:115839589	GCTTGGGGTATCCCC[-/G]AGGCTCTACCTGCTG	217325
rs247696056	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115842655	GTCTGTAGCTCCTTG[A/C]ACACCAACGGTGAAA	217325
rs247864958	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115838374	TAATGGAGGCTGGTG[C/T]AGTGGACAGGTTTCA	217325
rs247925402	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115830409	GGTGGGGGTGGGGGG[C/G]TCCTTGTCACTGGTC	217325
rs247933407	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115847979	CTTCTCACCACTGCA[G/T]TTGGGAAGAAATGGG	217325
rs247975359	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115840365	GAGTGGTCACAGTCC[G/T]TGGGACTCTGAAGGA	217325
rs248184227	in-del	-/TA			intron-variant	Llgl2	Mm_Celera	11:115844012	CCAGAGCCTTGTTAT[-/TA]TATAGTTCAACCTTA	217325
rs248226317	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115841565	CAAATGTACTTTCTT[C/T]CTTTTGTTGTTGTTG	217325
rs248226508	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115849107	CAAGCAGTTCACATG[C/T]AGAGGCCGCTCTGTG	217325
rs248258204	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115842574	AGGGTAGGTAGCTGT[A/T]GGGAAGCAGAAGCCC	217325
rs248266487	in-del	-/CAC			downstream-variant-500B	Llgl2	Mm_Celera	11:115856218	TACTTGGTTGAGGAA[-/CAC]CCCCCTCCCCCAGTT	217325
rs248336710	snp	A/C/T			intron-variant	Llgl2	Mm_Celera	11:115828086	AGTGGCCTTTGCCTG[A/C/T]GTCTTGAGAGCAGAA	217325
rs248460711	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115832177	CCTATGCAGTGGTGA[C/T]CGTGGGTAAGTTGCT	217325
rs248468650	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115841272	GAGACTGGTGTGAGC[C/T]GCCATGTGGATGCTG	217325
rs248507776	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115842031	TCAGCCAAGGCCTCG[A/C]AGGGCCCCGGGAGAG	217325
rs248575330	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115836223	GGAGTTTGTCATGAC[A/G]CCTGCCCCTGGAAGC	217325
rs248613921	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115846305	ATCTTAGCTCCAGCT[C/G]CCACGGGGTCTGCTG	217325
rs248618290	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115837794	GAGTGCTTGGCTAAA[C/G]GCCACAGAATCAAAG	217325
rs248643772	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115838181	GGGGACCAAGTCTAG[C/G]TCAGGGGCTGGGTGC	217325
rs248791710	in-del	-/GCCCA			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	Mm_Celera	11:115823003	GAGGCCCAGGACTTG[-/GCCCA]GGTTAGGAGAAAGGA	217325
rs248927817	snp	A/T			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115825058	AACCTCTAGAGATCC[A/T]GTGTTAAAGTCCATT	217325
rs249053190	snp	A/G			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115853419	ATTGCTTGTGGTGTC[A/G]GAGGAGCAATTCAAG	217325
rs249068098	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115851371	GCACAGTTGTTGTCT[G/T]AGTCAGGTCACTGTT	217325
rs249107722	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115848502	CAGGTGGAGACGCAG[C/T]CTGGAAGGCCATCTT	217325
rs249180879	snp	A/T			intron-variant	Llgl2	GRCm38.p3	11:115830981	ACAGCAGTGGCAGCC[A/T]GAGGAGCCAGGAAAG	217325
rs249197613	snp	C/T			downstream-variant-500B	Llgl2	Mm_Celera	11:115856098	CCTCCCCTCAACAGG[C/T]CACCCCTGAAAAGCC	217325
rs249231278	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115845838	TTCCAGGACAGCCAG[A/G]GCTACACAGAGAAAC	217325
rs249296859	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115849895	TAGGGGACTTTAGTG[A/G]CTACTTTCCCTGTTC	217325
rs249438574	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115836531	AACCTTGGTTCCTGT[A/G]TGCTGTGGGTGAGGC	217325
rs249477698	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115844339	TGACTGAGTGCGCCC[A/G]GCCATGACCACTGCT	217325
rs249478011	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115828381	AACCAAAGAAGAGGG[C/T]AGGATGTGCCACAAT	217325
rs249498428	in-del	-/AC			intron-variant, downstream-variant-500B	Llgl2	Mm_Celera	11:115855432	CTTCCCTGCCCACCT[-/AC]TGTCCTGACCTACTG	217325
rs249502375	in-del	-/GGA			intron-variant	Llgl2	Mm_Celera	11:115837312	AGTGTGAGTGTGTGT[-/GGA]GGGGGGGGTGGATAA	217325
rs249509178	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115835952	CTGTTCTACTTTTCC[A/G]TTTGAGAAGTATCGG	217325
rs249514896	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115845037	TCATCTCTTGGGTCC[C/T]GTTGAACCCTTGGCA	217325
rs249549112	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115836916	GAGGGTAAAGTCAGA[C/T]TCCGGAGTACTTGAG	217325
rs249556903	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115852633	CTGCTGGCTGTGAGC[A/G]GTGTCTGCTGTGTCC	217325
rs249620079	in-del	-/AC			intron-variant	Llgl2	Mm_Celera	11:115829655	AGGAATGTTCTCCTG[-/AC]AGGGGAATTTTGGGG	217325
rs249626596	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115842629	ATCAGCTGTTGGCAT[C/T]CGCACCTCCTGTCTG	217325
rs249805657	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115831283	CCTGAGTAGGGGATA[C/T]GAGGAGAAAGTAGCA	217325
rs250046333	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115829829	TTGAGGGATCTGAAC[C/T]GGGAGATGGCTCACG	217325
rs250084917	in-del	-/TGGGGA			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115824882	GGTTTGGGGGGGGGG[-/TGGGGA]GTTGGTGGACACACT	217325
rs250385495	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115837946	GTCAGGCAGCGTGTC[A/G]TGGGCAATGCGTGCA	217325
rs250418774	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115826526	AGCAAGGCAGAAGGG[A/G]ATTCCTTTGCCTGTC	217325
rs250429635	in-del	-/C			intron-variant	Llgl2	Mm_Celera	11:115833367	TTTAGATAAGAAGCA[-/C]CCCCCCTTCCCCAGT	217325
rs250498517	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115827522	ACTGGCAGCTCGCCC[C/T]GCTCTGGTTCTGGGA	217325
rs250550651	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115834206	CACTGCACGGAGGGA[A/G]GCTGTGAAGTTTCTC	217325
rs250583168	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115835282	TCTACCTATGACAGG[C/T]ACAAAACTTTCAGCC	217325
rs250616412	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115835785	GACATTTTTGGTACT[A/G]AGGATTGAGCCCAAA	217325
rs250651631	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115827832	GAATTCTTGAGCTAG[G/T]AGAGGCTCCTTTGGG	217325
rs250657500	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115844273	TCCCCAACCCCCCCC[A/C]CACACACACACACCC	217325
rs250676586	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115830862	CTTTTCTGGCTGAGC[C/T]AACCCCTAGCCTAAA	217325
rs250748365	in-del	-/TG			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823386	CCCAGTTTGTTACTC[-/TG]AGCCCCTCACCCCTA	217325
rs250832599	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115854090	ATGTGGAGCTCTGTC[A/G]GGCAGGCTCTGTCCC	217325
rs250874297	in-del	-/A			intron-variant	Llgl2	Mm_Celera	11:115846448	AGGGTCTCTCTAGAC[-/A]ACTCTAACTGTCTCA	217325
rs250915888	in-del	-/A			intron-variant	Llgl2	Mm_Celera	11:115852398	GGTACTTCCGGTGGG[-/A]AAATCACATAGGCAG	217325
rs250961748	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115830821	TTTGAAGGTCAAGCT[C/T]GGGTCCTCATGCTTT	217325
rs250995525	snp	A/G			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115824501	GGACACAGTGAGCAG[A/G]GACACCGTTCCCAGA	217325
rs250997511	snp	G/T			intron-variant	Llgl2	GRCm38.p3	11:115831403	GCTGTGAACACATAG[G/T]GCCAAGAGGCTGACC	217325
rs251035357	snp	A/G			intron-variant, nc-transcript-variant	Llgl2	Mm_Celera	11:115825222	CGGCAGGAGGACAGT[A/G]GAGGAAAAGATGTCT	217325
rs251037860	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115849333	TCAGGCTCTGAGGGG[C/T]ACCGGTGTCAGCAGC	217325
rs251165287	in-del	-/TGTGTGTGTCTGTC			intron-variant	Llgl2	GRCm38.p3	11:115827079	GTGTGTGTGTGTGTG[-/TGTGTGTGTCTGTC]TGTCTGTCTGTCTGT	217325
rs251183841	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115835454	GAAAAAGCTTTCTCT[G/T]CAGGCTCCAGCCTGG	217325
rs251237109	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115827456	GAGCTGGGTACCACG[A/G]GAGGCTGGAGAAGCT	217325
rs251245655	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115853498	TCAGCCCCTGGGTGG[A/G]TACAAACAAGGACAG	217325
rs251260174	in-del	-/TTTTTTT			intron-variant	Llgl2	Mm_Celera	11:115841392	GTCTCTAAATTCTGA[-/TTTTTTT]TTTTTTTTTTTTTTT	217325
rs251413498	in-del	-/T			intron-variant	Llgl2	Mm_Celera	11:115825890	TACATTTAAATTTTA[-/T]TTTTTTGTGTGTGCG	217325
rs251460686	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115840178	GACCCTAGCAGCCAG[C/T]CGCAGCCTAGGGACA	217325
rs251490868	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115841326	GAGAGGAGTCTCTTA[A/G]TGGACTAGCCATCAC	217325
rs251493746	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115831921	GTCCCCCACAAGGTC[A/G]CTGAGCCCTGCAGGT	217325
rs251524886	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115833112	GGTCCCTGGTGTTTG[A/G]TTTGGAAGTGGCTTG	217325
rs251532887	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115841537	TAGTAAAGACACTTC[A/C]CTGTGGCAGAACCAA	217325
rs251592493	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115833257	ATTGATTACAGAGCT[G/T]AGGATGAAGGGCCTT	217325
rs251612508	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115850582	GAGTCCTTTGCTGAC[C/T]GGGCTGTCTAGCCTC	217325
rs251654304	snp	A/G			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115844900	GAAGGTCAAGGGCGG[A/G]GTGTCAGAGCTGCAG	217325
rs251733565	in-del	-/T			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115822270	CATGGGAACCCAAGA[-/T]TCCCCCATCCTTGGC	217325
rs251764881	in-del	-/G			downstream-variant-500B	Llgl2	Mm_Celera	11:115856030	GCCAGAGTTCACCCT[-/G]GGGGAACGAGTGGGT	217325
rs251866097	in-del	-/C			intron-variant	Llgl2	Mm_Celera	11:115830291	TTTCCGAGGTGATTT[-/C]CAGTGTATTCTACCT	217325
rs251884911	snp	A/C			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115822446	CCTGAAGCACTCATC[A/C]AAGCCATGGAGTTTG	217325
rs251916065	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115836952	GAAGAGTCTTATCCA[C/T]GGCAGCCACTCGCCC	217325
rs251967056	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115837607	GAGAACAGGATCATG[G/T]TGAAGCATCTAGTCC	217325
rs251967179	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115828618	TAGGAGACCCTAGGA[C/T]GAGGTTGGCCTAGGA	217325
rs251993573	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115840009	GCTCAGGCCTGGCTT[A/G]GCCTCCTCTAAGGAG	217325
rs251995518	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115854189	CTCTTCTGCCTCTCC[C/T]CAGGTTTCTATCTGA	217325
rs252246335	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115845647	CTACCTGTTCCCCAG[G/T]TGCGTCTCAGTCAAC	217325
rs252357127	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115851596	CTTGGGGAGGAAAGG[A/G]CTTATTTGGCTCACA	217325
rs252357466	in-del	-/AC			intron-variant	Llgl2	Mm_Celera	11:115826374	CTGGGAATGGACCTT[-/AC]ACGTCTTCTGGAAAA	217325
rs252358269	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115845198	AGTTCATGTTCCCTG[C/T]TGCCTGTAAAGTGGT	217325
rs252364835	snp	C/T			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115850728	CCGCTGGAAGGGGCA[C/T]GAGCGCCTCGCCGCC	217325
rs252394958	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115845778	CTTGGGAGGCAGACA[C/T]AGGCGGATTTCTGAG	217325
rs252431902	snp	A/G			upstream-variant-2KB	Llgl2	Mm_Celera	11:115823961	CTGCCCCGTCGGCTC[A/G]GCCTAGGAGGCGGGG	217325
rs252451778	in-del	-/CAGGA			intron-variant	Llgl2	Mm_Celera	11:115839466	CCTGAGCCCAGGTAG[-/CAGGA]CAGGACAGGACAGGA	217325
rs252641268	in-del	-/T			intron-variant	Llgl2	Mm_Celera	11:115838254	TGGAGCCATATAGCC[-/T]GGGCCTTGGTTCTGA	217325
rs252642071	in-del	-/T			intron-variant	Llgl2	GRCm38.p3	11:115847502	TGCACAGAGGAATCC[-/T]CCCCCTCACAGGCTG	217325
rs252732779	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115828445	ACTTGCCAAGAGGAC[A/G]GCTTTCGAGCTAAAG	217325
rs252842497	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115845906	aaacaaaaacaaaaa[A/C]aaaaCTGAACAAggg	217325
rs252853531	snp	C/T			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115851011	CACTTCCTCAAGGTG[C/T]ACACTTCACCCCAGT	217325
rs252970804	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115825276	CTTTTCTCTTTAAAT[A/G]TTTATTTGTTTGTTT	217325
rs252992852	snp	A/C/G			intron-variant	Llgl2	Mm_Celera	11:115825848	CTGTGTTGGAAAAAA[A/C/G]AAAAGAACAAAATTT	217325
rs253116292	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115852333	TGGGAGACACTCATG[A/G]CGTGAGGCCACGGAG	217325
rs253119767	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115848759	AAACAGACAAGACAA[A/G]GGTTGACATAGACCC	217325
rs253150692	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115852703	GTGGAGATTCTCATG[A/G]GAGTGTGGGAGTTCT	217325
rs253250512	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115835713	AGGTCCGAGACAGCA[A/G]CAGGATCCTTTCTCC	217325
rs253315709	snp	A/G			intron-variant, downstream-variant-500B	Llgl2	Mm_Celera	11:115855325	AGGCGGTCCTTAAAA[A/G]AACTGCCACCCCTCC	217325
rs253335965	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115827741	CCAGTTTCTTTGAGA[C/T]GGCTTTCTCCGTCTG	217325
rs253499290	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115843700	CTACCACGTTGTCCA[A/G]GCTAGTTGTATAGTC	217325
rs253511680	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115850355	CAGGTAGCAGGCTGG[A/G]CAGGGTGGGGTTGAG	217325
rs253527718	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115835642	CCAGCAATCTGGAGC[C/T]GCTTGGGGATAATTA	217325
rs253539064	in-del	-/CGCT			intron-variant	Llgl2	Mm_Celera	11:115828967	AGGGCCCTGCCCTGC[-/CGCT]CGCTCTAGCCGTGGG	217325
rs253623363	snp	A/C			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115853122	TGCAGAAAGAAGAAC[A/C]GATGAACCTGTCCGG	217325
rs253685643	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115847710	AACGTCCCAGGCTCC[C/T]GCCCAGGGAGACAGT	217325
rs253834119	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115838616	AGCCCCATGTTCAAT[C/T]GCTTCTTATGGGCAG	217325
rs253860771	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115833233	AGCAAAGTCTTGGCC[C/G]TTTAATTGATTGATT	217325
rs253866036	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115830700	GAGCCACAGGGGTCC[G/T]CCTCCCGGAACTCGC	217325
rs253892866	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115826069	GCCATCTTGCCAGCC[A/C]TAAAATAACCTTCAA	217325
rs253920064	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115826541	GATTCCTTTGCCTGT[C/T]GTCTTTTCTTCACAC	217325
rs254023051	snp	C/T			intron-variant	Llgl2	GRCm38.p3	11:115845573	GGGCCACGGCCTTCT[C/T]CTGGGCCCCAGTAAG	217325
rs254056592	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115837347	CAGGAAAGTGAGCAT[C/T]CAGGAGGACTGTGGG	217325
rs254102854	in-del	-/T			intron-variant	Llgl2	Mm_Celera	11:115834238	TTCTGGATTTTTATG[-/T]TTTTTTTTTTCTTTC	217325
rs254186980	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115825776	AGATCTCTGAGCTCG[A/G]GGCCAGCCTGGTCTA	217325
rs254304949	snp	C/T			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	Mm_Celera	11:115822869	CTAGGTGTCTTCTGT[C/T]TGTAGGGACGTGCAC	217325
rs254345937	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115829184	CCTAGAGAGCAGGAC[G/T]GTTGCTGGGCATGGC	217325
rs254348698	snp	A/C			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	GRCm38.p3	11:115823448	TAGGGGCTGACAACC[A/C]CCTTGAACCTCAGGC	217325
rs254425260	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115832950	TCCCACCAATCCCCA[C/T]GCCCCACCCCACCCA	217325
rs254469358	snp	C/T			upstream-variant-2KB	Llgl2	Mm_Celera	11:115823917	TGGTTGGAGAGCGGC[C/T]CCGCTCTGGAGACTC	217325
rs254641809	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115826865	GAAGTCAGTGGAGCT[A/G]AAGATCAGAATTTTA	217325
rs254687936	in-del	-/ACA			intron-variant	Llgl2	Mm_Celera	11:115842930	AACTGTACACTGTGC[-/ACA]ACACCCCTTTAATCC	217325
rs254756525	in-del	-/C			intron-variant	Llgl2	Mm_Celera	11:115833836	GGGTCTCACTTTGTA[-/C]CCCTTCATGGCTTTA	217325
rs254882777	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115845300	CTTTCCCCAGGGCTG[A/G]TAAAGCCATTGCATC	217325
rs254884751	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115836598	CTTTAGTATGCTCCA[C/T]TTGTGGTCCCCAAAT	217325
rs254907600	in-del	-/AC			intron-variant	Llgl2	GRCm38.p3	11:115848099	GGCTTTGCCCTGTAT[-/AC]TCCATCAGGTCCCAG	217325
rs254922958	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115837136	CTGTTGTGCTGAGAG[A/G]ATTGTCCTGGGCGCT	217325
rs254929159	in-del	-/CA			intron-variant	Llgl2	Mm_Celera	11:115825384	GGCTGGCCTTGAACT[-/CA]CAGAGATCCACCTGC	217325
rs254938898	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115826934	GTGCTGCCTCTTCTA[G/T]ACTTGACACCTCTTC	217325
rs255226057	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115840529	ACTTCCCTGAGGATG[A/C]GAAGTCAGAATATTC	217325
rs255232477	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115850402	GGTTTGGGGGGGGAG[A/G]CGGGAACCCCTGCCC	217325
rs255273688	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115832441	AGGTACATTCAGGGG[C/G]TCTGGAACAGTGCTG	217325
rs255313349	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115833470	ACATGCAGCGTTCAG[C/T]GAGCTGGCGGCTATG	217325
rs255514539	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115847325	GCTTCTGTGTAGAGG[A/G]TCTAACCTTGTCTTC	217325
rs255553371	snp	A/C			intron-variant	Llgl2	GRCm38.p3	11:115847838	ATCCCTTCCTTCAAC[A/C]TTCCCAGAGAGGTGC	217325
rs255643187	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115849032	CACCTCTCCAGCCCC[C/T]TCCTCCCCTCTTATT	217325
rs255702950	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115849307	TCCCTGACTGAGCTC[A/C]GGGCCTCTTGTCAGG	217325
rs255773390	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115843610	TCTTCTCTTCTCTGG[C/T]TACTCACGTCCCCGT	217325
rs255799728	in-del	-/CCAC			downstream-variant-500B	Llgl2	Mm_Celera	11:115856217	TACTTGGTTGAGGAA[-/CCAC]CACCCCCCTCCCCCA	217325
rs255800073	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115827145	CTTACTCCATTCACT[C/T]TACACTCCGTCTAGG	217325
rs256016821	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115830261	GCAGATAAACCAGAC[A/G]CCGATGCCATAACCT	217325
rs256054928	snp	C/T			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	GRCm38.p3	11:115823535	GGTTCGCCATTACGT[C/T]TTCGTTCCCATACCA	217325
rs256202247	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115846549	GATCAAAGGTGTGTA[C/T]TACCACACTCGATTT	217325
rs256254914	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115838473	ACATGCGTGGCTGGT[C/G]CTTCCAGAGATCAGA	217325
rs256357907	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115850226	CTCACAGGCATCCCC[A/G]TCCCTTGGCAGGTGG	217325
rs256395111	snp	A/G			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115822136	AGATGATTGAGCAGT[A/G]CCTCTGGCTGCTGCC	217325
rs256401402	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115843816	CAACACCTGGTATTC[C/T]TGATGTCTAACCTAC	217325
rs256435796	in-del	-/TTGTGTGTGTGTGTGT			intron-variant	Llgl2	GRCm38.p3	11:115840885	GTAAGTTGTTTTGAC[-/TTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTT	217325
rs256596399	snp	C/G/T			intron-variant, downstream-variant-500B	Llgl2	Mm_Celera	11:115855433	TTCCCTGCCCACCTA[C/G/T]TGTCCTGACCTACTG	217325
rs256638621	snp	G/T			downstream-variant-500B	Llgl2	Mm_Celera	11:115855960	GGGTGACTATGCAGC[G/T]TCTGTCTGTCTGTCC	217325
rs256855485	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115830394	TGAGCCCCTTCACGG[C/G]GTGGGGGTGGGGGGG	217325
rs256896709	snp	A/T			upstream-variant-2KB, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115823558	CCATACCACTTTACT[A/T]GTGGGTCTGAAACCT	217325
rs256938883	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115840939	GATTTTTTTTTAATT[A/T]ATTAATTTATTTATA	217325
rs257010708	snp	C/T			missense, nc-transcript-variant	Llgl2	Mm_Celera	11:115849519	CCTGTTCTCCAGCCT[C/T]TGATGACCCCTACGC	217325
rs257053354	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115852507	CCTTGCTCCACTGAG[C/T]ACTACAAGTATGGAC	217325
rs257092257	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115852962	AGGCTGGGTGGAAGC[C/T]CGGGTTGCTGGCCCC	217325
rs257200901	snp	C/T			downstream-variant-500B	Llgl2	Mm_Celera	11:115856126	GCCTTTATGAGAACT[C/T]CTCTGTAGTAATACA	217325
rs257414412	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115825306	TGTTTATTGGTTGGT[A/T]GATTCATTCAGACAG	217325
rs257496176	in-del	-/TTCAA			intron-variant	Llgl2	Mm_Celera	11:115837484	TAGACCAGGCTAGCC[-/TTCAA]TTCAGAGATCTACTT	217325
rs257522690	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115837274	GTTGCTCTCCTCTGA[A/G]AATGTCTAGAATGGG	217325
rs257564012	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115850939	GCAGGGCATCCATCC[A/G]GGGCTTGGGACTGGG	217325
rs257565740	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115829056	TGGCCTCACACAGGA[G/T]GTTGGGCTGGGGCAG	217325
rs257601291	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115829744	CTGGTTCCACACACA[A/C]AGCATAGATCTGTGT	217325
rs257602119	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115845088	GCTACCACCATCTCG[C/T]GCTCTGGAACTCCTT	217325
rs257637164	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115838433	ATATGTATGCATGTT[A/T]TGCCTTCATGTATGT	217325
rs257672496	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115830588	GTGTTTGTGGTAGGG[C/T]GGACAGGTCTCCTTC	217325
rs257805020	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115830992	AGCCAGAGGAGCCAG[G/T]AAAGGGCCAAACGAG	217325
rs257846636	snp	C/T			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	Mm_Celera	11:115822814	CTCTCATATAGGACT[C/T]ACCTGGATGGAACCG	217325
rs257927354	snp	C/T			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115843349	CCCACACCAGCCCAG[C/T]GCCCTTGGCTATAGC	217325
rs258011773	in-del	-/C			intron-variant	Llgl2	Mm_Celera	11:115845889	AAACAAAACAAAACA[-/C]AAAACAAAAACAAAA	217325
rs258023907	in-del	-/G			intron-variant	Llgl2	Mm_Celera	11:115835036	GGCATCCCCTAGGAA[-/G]GAGGTATATTGTTAT	217325
rs258026153	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115826796	TTTTAGGTAGACACC[C/T]GGCCGGCTGAGGGGA	217325
rs258044838	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115835600	GACAGGGTGTGACAG[A/G]GCTCATTAGCTTCCC	217325
rs258080531	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115827559	CTTATCTCCCTCAGT[C/G]ATACTGCTCTCTCCC	217325
rs258154836	in-del	-/TC			intron-variant	Llgl2	Mm_Celera	11:115846677	TTGAGGATTATAGTG[-/TC]TCTCATCATAGTGTC	217325
rs258213305	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115828294	TTTTCTTCCTTTCAA[A/G]TGGGCAGGACAGGAA	217325
rs258354420	in-del	-/C			intron-variant	Llgl2	GRCm38.p3	11:115847501	ACTGCACAGAGGAAT[-/C]CCCCCCTCACAGGCT	217325
rs258651033	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115843053	AAAATGATATATGTG[C/T]GTAACTATACATGTG	217325
rs258660802	in-del	-/GTTTTTTTTTGTTTTTT			intron-variant	Llgl2	GRCm38.p3	11:115851431	GTGTGGAGGAGAGGG[-/GTTTTTTTTTGTTTTTT]TTTTTTTTTTTGGTT	217325
rs258694059	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115834913	ACAAGGTAAGGATGC[A/G]GTGAGGGAGGGCAGG	217325
rs258862267	in-del	-/G			intron-variant	Llgl2	GRCm38.p3	11:115828767	GCTTCCCACGCTTTC[-/G]GGGGGCCCCTTCCCG	217325
rs258939125	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115846324	CGGGGTCTGCTGCCT[C/T]GGGCCTCTACTGACA	217325
rs258968642	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115838240	GTTGGGGCAGGGAAC[C/T]GGAGCCATATAGCCG	217325
rs259088117	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115827376	ACAGACAGACCCTCC[G/T]ACCTTGTGGGGAGCC	217325
rs259196260	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115839706	GGCCACCTCACCCTT[C/T]AGGGACCTAACTAAG	217325
rs259270926	snp	C/T			downstream-variant-500B	Llgl2	Mm_Celera	11:115856054	AGTGGGTTTATTGGA[C/T]TTCCTAGTAGAACAC	217325
rs259294841	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115836744	CCTGGCTCTGTAAGA[C/T]GTGAATTGGTAAGGC	217325
rs259310964	snp	A/T			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115850047	CGGTGTGTGCTTACG[A/T]CTGCTCTACAAACTG	217325
rs259344817	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115850479	GGGTGCTAGATTAGC[A/G]TGACCCCAGAGTGAT	217325
rs259400952	snp	A/T			intron-variant	Llgl2	Mm_Celera	11:115844107	TCAGGGCAAGGCCGC[A/T]GGGGGTGCCCCCCTA	217325
rs259521408	snp	A/G			intron-variant	Llgl2	GRCm38.p3	11:115848035	CTGGAGACTGGCCTC[A/G]TTCAGGCCTTGGGAT	217325
rs259563526	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115854523	CCTAGTGGTCCCTAA[C/T]CCTCATTGTCTGCCC	217325
rs259600859	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115848921	CCCAGGGAGACCCTA[G/T]GCCTGTGTTTGCTTC	217325
rs259736165	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115849243	CATCAGGGTGTCAGT[C/T]AAGGCCAAACATTAG	217325
rs259738021	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115842533	TTGGGCCCTGCTTCA[A/G]CCTACTGCAGCAGAG	217325
rs259749850	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115839724	GGACCTAACTAAGGC[A/G]GGGGATTACTAGCAT	217325
rs259755249	snp	C/T			synonymous-codon, nc-transcript-variant	Llgl2	GRCm38.p3	11:115848258	CTGCATCTCAGTGGT[C/T]CACAACGGCCAGCAG	217325
rs259769101	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115833943	AGATGCCCAGTCAGA[G/T]CTCAGGGAGCTAGCT	217325
rs259795649	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115840465	AGCTGACGGGGCAGG[G/T]CGTGGCCTCAGAGGC	217325
rs259866706	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115833811	GCCTCCTTAGGGAGT[A/G]GCAGGAAATAGGGTC	217325
rs259910005	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115826458	AAAAAAAAAAAAAAC[A/C]CGAGGGAATGGAAAT	217325
rs259999310	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115837778	TACACGTGTGTCCAC[C/T]GAGTGCTTGGCTAAA	217325
rs260060841	snp	A/G			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115825044	CCTTATGTCGACGCA[A/G]CCTCTAGAGATCCAG	217325
rs260060860	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115832095	GCCATTCCTCATGGA[C/T]GCCTTTATAAGCCCC	217325
rs260138192	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115829466	CACGTGAGACAGGGG[C/T]CACCCCTGTGCAGTT	217325
rs260210788	snp	C/G			upstream-variant-2KB	Llgl2	Mm_Celera	11:115823651	CTTACTAGACAGCCG[C/G]GGGAGGGAAGTGAAG	217325
rs260249403	snp	A/G			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115824572	GCTTCCTGTGACCCG[A/G]CGTCGCCAGCGGCGT	217325
rs260329449	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115835807	GAGCCCAAACCATCT[A/C]AGTAACCAAGCCATC	217325
rs260392892	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115828339	TAATCATGCATTTGC[A/G]AATGACACCAGCTAT	217325
rs260407081	in-del	-/AG			intron-variant	Llgl2	Mm_Celera	11:115833204	CCCAGTCTTAAATCC[-/AG]AGTCTTTTCATAAGC	217325
rs260417239	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115828636	GGTTGGCCTAGGACC[A/G]GGTAACTCAGTCAAG	217325
rs260484294	snp	G/T			missense, nc-transcript-variant	Llgl2	Mm_Celera	11:115853801	CGGCGAGTCGGTGTC[G/T]CCCACTTTGGCAGCT	217325
rs260520422	snp	C/T			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115822350	CCTGGGCTTGCTCAG[C/T]AGAAAGGAATTGATT	217325
rs260604758	snp	A/T			downstream-variant-500B	Llgl2	Mm_Celera	11:115855929	TCACCAAGCGTTGCT[A/T]ACTTTCCAGGAGTAG	217325
rs260649786	snp	G/T			intron-variant	Llgl2	Mm_Celera	11:115851341	TTATGTTAGAGTTAA[G/T]TCCCGAGCAAATATG	217325
rs260831198	snp	A/G			synonymous-codon, nc-transcript-variant	Llgl2	Mm_Celera	11:115855088	GGAAATCCAGAGCAC[A/G]CTGGAGGGGGACCGG	217325
rs260839498	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115828119	GGACCATGTAGATTC[C/T]ACCTCAGCATCTTTA	217325
rs260857001	in-del	-/TC			intron-variant	Llgl2	Mm_Celera	11:115827082	GTGTGTGTGTGTGTG[-/TC]TGTCTGTCTGTCTGT	217325
rs261004004	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115834151	TCCAGTTGAGGCACC[A/G]ATCAAGAAATTCCAC	217325
rs261036158	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115826573	GTACCTCACTCATCC[C/T]AGGCATCAGATGACT	217325
rs261121894	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115838944	ATAACACACCCCCCT[A/C]AGAACCCTCCCCACC	217325
rs261182190	in-del	-/AAAA			intron-variant	Llgl2	Mm_Celera	11:115825841	GAAACCCTGTGTTGG[-/AAAA]AAAAAAAAAAAGAAC	217325
rs261313825	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115851918	AAATTAGCCAGCACA[A/G]TCATCCTATTATTTT	217325
rs261340826	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115846067	ACACACACATGCTAA[A/G]CTCATATACATAAAA	217325
rs261351160	in-del	-/T			intron-variant	Llgl2	Mm_Celera	11:115850388	AGAGTGGTTGGGTGG[-/T]TTTGGGGGGGGAGAC	217325
rs261367754	snp	A/C			intron-variant	Llgl2	Mm_Celera	11:115846373	TGCCTACACAAGGGC[A/C]CACACATGTGTACAT	217325
rs261369181	snp	C/T			intron-variant	Llgl2	Mm_Celera	11:115830781	TTACAGGCACACACC[C/T]CCACCCCAGCTCTTT	217325
rs261399414	snp	C/G			intron-variant	Llgl2	Mm_Celera	11:115835477	CAGCCTGGGAGGAGG[C/G]GGGGGGGGAAGAGCA	217325
rs261429258	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115827463	GTACCACGGGAGGCT[A/G]GAGAAGCTGACTCTG	217325
rs261479514	snp	A/G			intron-variant, upstream-variant-2KB	Llgl2	Mm_Celera	11:115824393	GTCTTTTCCTGTTCC[A/G]CCCCCCGGATTACCA	217325
rs261581452	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115833336	CCCAACCTTCAGGCT[A/G]TCTTTCCAGCCTCGG	217325
rs261647826	snp	C/T			upstream-variant-2KB, utr-variant-3-prime	Llgl2, Tsen54	Mm_Celera	11:115822792	TCTCAGGGGCCGTGC[C/T]AGCTGTCTCTCATAT	217325
rs261667084	in-del	-/C			intron-variant	Llgl2	Mm_Celera	11:115841892	TTATCCCCCACCCCA[-/C]CCCCCAGTCCTCCAA	217325
rs261751201	snp	C/T			intron-variant, downstream-variant-500B	Llgl2	Mm_Celera	11:115855427	GGCACCTTCCCTGCC[C/T]ACCTACTGTCCTGAC	217325
rs261777156	snp	A/G			intron-variant	Llgl2	Mm_Celera	11:115828794	CCCGGGCACTGCTCG[A/G]ACATTCTGAGTAGCT	217325
rs261793594	snp	C/T			upstream-variant-2KB, intron-variant, downstream-variant-500B	Llgl2, Tsen54	Mm_Celera	11:115822403	GTAGTTAAGAACCCA[C/T]ACCTCCTATCCCTCT	217325
rs261937253	snp	C/T			synonymous-codon, nc-transcript-variant, downstream-variant-500B	Llgl2	Mm_Celera	11:115855231	CCGCGTGGCTGTGGG[C/T]TGCAGGCTCAGCAAT	217325

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