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

Rnf213

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs6210692	snp	C/T	0.5	0	missense	Rnf213	Mm_Celera	11:119408883	GCCAGCCTGGGCATC[C/T]CCTGGACACAGAGAA	672511
rs6211180	snp	A/G	0.444444	0.157135	missense	Rnf213	GRCm38.p3	11:119408952	GCGGCAGCCCTCTGC[A/G]GGGTCAGGCTGCAGA	672511
rs6211207	snp	A/G	0.5	0	missense	Rnf213	Mm_Celera	11:119408970	GTCAGGCTGCAGAAC[A/G]CACCGACGCTCAGAG	672511
rs6286851	snp	C/T	0.5	0	intron-variant	Rnf213	Mm_Celera	11:119464263	TCGGTCTAGCACTTT[C/T]GATCTAGCACCTTCT	672511
rs6288046	snp	A/C	0.48	0.0979796	intron-variant	Rnf213	GRCm38.p3	11:119464496	CTCTCATAAGCTACA[A/C]CCCTTAAAGGGGTGA	672511
rs6382383	snp	C/G	0.5	0	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475759	agacatcccagaaga[C/G]ggtatcagatctcat	672511
rs6382408	snp	A/G	0.5	0	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475778	atcagatctcattac[A/G]gatgtttgtgagcca	672511
rs6382901	snp	A/G	0.5	0	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475862	cactcataaccactg[A/G]gctatctctccagtc	672511
rs6382950	snp	C/T	0.5	0	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475885	ctccagtcccCACCC[C/T]GAANCTTTTAAAATA	672511
rs6382954	snp	C/T	0.5	0	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475889	agtcccCACCCNGAA[C/T]CTTTTAAAATAAGAT	672511
rs6382999	snp	C/T	0.5	0	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475927	AGAAGAAAGGGGCTT[C/T]CTGCAAACTGAACTC	672511
rs6384044	snp	G/T	0.5	0	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476047	ttttttttttttttt[G/T]ttttGGTGTGATTTC	672511
rs6384090	snp	C/T	0.5	0	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119476070	GTGATTTCACACAAA[C/T]GAGGGCATTCTAGAA	672511
rs6384210	snp	G/T	0.304688	0.243945	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476131	TTCATAGGTGTTGGT[G/T]TGTGCAGCAGCTGGA	672511
rs6384687	snp	C/T	0.304688	0.243945	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476155	AGCTGGAGTGGCTGA[C/T]GGTAGCACTGGGCAC	672511
rs6396556	snp	A/G	0.456747	0.140554	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119470683	CTGAGCACATCCATC[A/G]TCCACACTACGCATA	672511
rs13459989	snp	A/G	0.486111	0.0821678	utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119486265	AAAGTGTGGGCACAG[A/G]CTGGATTCAAGGCCT	672511
rs13459990	snp	G/T	0.46281	0.131194	utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119486369	CTTAAGTCTGATGAA[G/T]GATTGTCAGTCAACT	672511
rs13459991	snp	A/T	0.375	0.216506	utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119486533	GGGTAGTCAATTTTT[A/T]AAATTTTTTTACTTA	672511
rs13459992	snp	C/G/T	0.497041	0.0383476	utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119486721	CATGTAAACCCACCA[C/G/T]GAGCCACTGCCAACC	672511
rs27015052	snp	C/T	0.277778	0.248452	downstream-variant-500B, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119487627	TTCTGTGACAGTGTT[C/T]CTGCTGTAGTATCCA	672511
rs27015053	snp	C/G	0.473373	0.11227	utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119487094	AGAGTACCTGTCCTC[C/G]GATGTCTGCATCCCA	672511
rs27015054	snp	A/C	0.48	0.0979796	synonymous-codon, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119486146	ACGAAAATGGGACCG[A/C]CAATCAAGGTAGAGC	672511
rs27015055	snp	C/T	0.46281	0.131194	synonymous-codon, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119486014	TCACAGCCTCAAGGA[C/T]ACTCTAGTAAGTTAC	672511
rs27015056	snp	C/T	0.48	0.0979796	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119485981	GATGTTACAAAAACT[C/T]TCTCTTGTTCCTTGA	672511
rs27015057	snp	A/C	0.49827	0.0293608	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119485677	ATCATGTCTCGGGTT[A/C]TAAAACAGCCCTCTG	672511
rs27015058	snp	G/T	0.486111	0.0821678	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119485249	ACACTCATCAGCTAT[G/T]TGTGTATGGCACAAT	672511
rs27015059	snp	A/G	0.49827	0.0293608	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119485196	TCTTTTCATTTGTAC[A/G]TCCCGACTCTGAGGC	672511
rs27015060	snp	G/T	0.497778	0.0332592	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119485134	GTAAAGGCACAGTTA[G/T]CCCTCTCTGCCAAGT	672511
rs27015061	snp	A/G	0.489796	0.070696	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119484376	AAGTCAGAGGTTAGG[A/G]ACATGGCCCAGTAGG	672511
rs27015062	snp	A/G	0.48	0.0979796	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119484140	TGCCTTGGATACTTT[A/G]TAGATTTGGTTTGCT	672511
rs27015063	snp	A/G	0.277778	0.248452	synonymous-codon, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119483735	AGAACAGCGGCTGCG[A/G]CTGAACAAAGTGAGT	672511
rs27015064	snp	C/T	0.486111	0.0821678	synonymous-codon, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119483702	TGCTCTCTGGCAGTT[C/T]CTATCTGCACATAAG	672511
rs27015065	snp	A/G	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119483588	GCTCAAGACAGAAAT[A/G]GGGGAATGTGCCTAT	672511
rs27015066	snp	C/T	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119483459	ATCAGTAGACTGACA[C/T]ATGCTCTATGATGTC	672511
rs27015067	snp	A/G	0.277778	0.248452	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119483434	TCTGCCCTGTACACC[A/G]TATACTTGGATCAGT	672511
rs27015068	snp	C/T	0.277778	0.248452	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119483326	TCAGCATGACCCTTG[C/T]CAAAAGCTCCTGCTT	672511
rs27015069	snp	A/G	0.49827	0.0293608	missense, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119482958	AACTTAGCAATCAGT[A/G]CCATCAGCGGACAGC	672511
rs27015070	snp	C/T	0.49827	0.0293608	missense, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119482947	GCTCACTCCCTAACT[C/T]AGCAATCAGTACCAT	672511
rs27015071	snp	C/G	0.277778	0.248452	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119482816	GCCTGCATCAGGCTA[C/G]TGCCTTCTGGAGAGC	672511
rs27015072	snp	C/T	0.277778	0.248452	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119482719	TCACAGTTATGTGTG[C/T]TGTGGCTAAACAGCC	672511
rs27015073	snp	C/T	0.277778	0.248452	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119482542	GCTCCAGCTGCATCA[C/T]AGCTACTGTGAACAT	672511
rs27015074	snp	G/T	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119482287	CTTGAATAGCTGGGT[G/T]CTGCTACTGAGTCAC	672511
rs27015075	snp	C/T	0.260355	0.249785	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119482253	CCTGGGGCAACACTG[C/T]GGGCTTTACCAGAAA	672511
rs27015076	snp	A/G	0.5	0	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119482083	TGCAGTGACTCCCTT[A/G]GTGAATGAGCTATCC	672511
rs27015077	snp	A/G	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119481612	GGTTTTTCTGCAATT[A/G]TTAATAGCACCACCA	672511
rs27015078	snp	C/G	0.32	0.24	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119481542	CAAGCTCTTTGGACT[C/G]TCTGCACCTCAGTCC	672511
rs27015079	snp	C/T	0.260355	0.249785	synonymous-codon, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119481311	ACGGCAGATCAGCAG[C/T]CGGTTCCTACAGGGC	672511
rs27015080	snp	A/G	0.277778	0.248452	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119480650	GTATTAGATGGGATG[A/G]CCATGTCTGTGAGCC	672511
rs27015081	snp	A/G	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119479673	GTCACAGTTCAGGTA[A/G]GACTCTATTCAAGCT	672511
rs27015082	snp	A/G	0.244898	0.249948	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119479480	AAAATGTACAAGCTC[A/G]CTAGCATTCCTTAGG	672511
rs27015083	snp	A/G	0.231111	0.249285	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119479346	CTGAAAGCCATTTGT[A/G]GGTACTTAGAGAAAG	672511
rs27015084	snp	A/C	0.35503	0.226867	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119479334	AAGAGTGTAACCCTG[A/C]AAGCCATTTGTGGGT	672511
rs27015085	snp	A/G	0.432133	0.171253	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119479255	AGGATTTAGTCCTCA[A/G]GGCAGTTCTACCCAT	672511
rs27015086	snp	C/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Rnf213, LOC102639982	Mm_Celera	11:119477930	TCTCACATATCCAGC[C/T]AGTCACACAAACACA	672511
rs27015087	snp	C/T	0.32	0.24	intron-variant, nc-transcript-variant	Rnf213, LOC102639982	Mm_Celera	11:119477829	GTGTCAGTGCTGTGA[C/T]TTCTCTCAGGGTGGT	672511
rs27015088	snp	A/G	0.444444	0.157135	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	GRCm38.p3	11:119477784	TGACCCTGAGCACCA[A/G]TGTCGGGTATTCACA	672511
rs27015089	snp	G/T	0.32	0.24	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119477770	GGTGATCTTTGAGGT[G/T]ACCCTGAGCACCAGT	672511
rs27015090	snp	C/T	0.32	0.24	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119477706	GAGGTGCAGCAATCC[C/T]GTCGGACCCAGGAAC	672511
rs27015091	snp	A/G	0.231111	0.249285	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119477609	AGCAAACATTATTCA[A/G]CGCGTGAACATTTGT	672511
rs27015092	snp	C/G	0.336735	0.234472	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119477499	AATAACACATAGGTC[C/G]GTCAGTAGTCATCAG	672511
rs27015093	snp	A/G	0.32	0.24	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119477430	AATATTAGTAGCAGG[A/G]AACTCAAGAAGGCCT	672511
rs27015094	snp	A/G	0.495	0.0497494	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	GRCm38.p3	11:119477307	CTCCAGAAGGTACGA[A/G]GGACTCCTGCTTGAC	672511
rs27015095	snp	A/T	0.444444	0.157135	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476870	AGGTGGAAGGAAAGC[A/T]GTGATTGTGGCATCT	672511
rs27015096	snp	C/G	0.495868	0.0452663	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119476642	TCTTTACCCATCATC[C/G]CTGGGGAGGGACTCC	672511
rs27015097	snp	A/G	0.32	0.24	synonymous-codon, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476506	AACCAAAGGATGCAG[A/G]AACAACTGGGAGAAG	672511
rs27015098	snp	C/G	0.32	0.24	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476402	TACCTGGTACTTACC[C/G]TATGCAGGATGCTAT	672511
rs27015099	snp	A/G	0.486111	0.0821678	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119476260	ACAGCAATGGAATCA[A/G]AGGAACTGTCTGAAG	672511
rs27015100	snp	C/T	0.444444	0.157135	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119474843	TCTAAGCATTTAAAT[C/T]TATCAAGGAAGGACA	672511
rs27015101	snp	C/T	0.231111	0.249285	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119474777	ACAGTTTCTCCTAGT[C/T]GGCTTTTTTTGAGCA	672511
rs27015102	snp	A/G	0.492188	0.0620098	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119474677	ATCACACAAGAATCA[A/G]TCATTAGCCTTGCTT	672511
rs27015103	snp	C/T	0.42	0.183303	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119474637	AGTGCAAACCTATTG[C/T]GTGGGAGACACATGC	672511
rs27015104	snp	C/T	0.231111	0.249285	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119474090	GATGCTGGTGTCTTG[C/T]TCTTCTGCCCTCTCC	672511
rs27015105	snp	C/T	0.475309	0.108333	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119474072	GAAGTCATCCTCTGA[C/T]TTGATGCTGGTGTCT	672511
rs27015106	snp	A/C	0.231111	0.249285	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473998	GCTGATGTTTTAGAT[A/C]ATCCCACAGCCAGCT	672511
rs27015107	snp	C/T	0.244898	0.249948	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473813	AGTCTGGTTTTCTTC[C/T]TAACTGATACCAACT	672511
rs27015108	snp	A/G	0.244898	0.249948	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473681	AGCCTAATCTCCAAC[A/G]TGGCAAGGAATAGGA	672511
rs27015109	snp	A/T	0.260355	0.249785	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473344	TTCTAATGTTCACCT[A/T]GTCTTCTCTTCCTTT	672511
rs27015110	snp	A/G	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473267	GTTCCCTCGGGGCAT[A/G]GAGCCCTACCTCCAA	672511
rs27015111	snp	A/T	0.124444	0.216185	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473092	ATTTTATGCAGCCAC[A/T]TTAAGCTGAGTCTTA	672511
rs27015112	snp	C/T	0.244898	0.249948	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119472944	TGTTCTACCAGACCT[C/T]GGATCCCAATTATTG	672511
rs27015113	snp	C/T	0.260355	0.249785	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119472668	GACACAGGAGTTAGA[C/T]AGAATGCTACTCCTG	672511
rs27015114	snp	C/T	0.231111	0.249285	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119472584	ATGCCTTGGTTTGTG[C/T]GAGGGGTAGGTTCTA	672511
rs27015115	snp	C/T	0.124444	0.216185	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119472162	CAATCTCTGCACATG[C/T]CACCTAACTTGAACT	672511
rs27015116	snp	C/T	0.32	0.24	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119472140	AACACACTGAGCCAG[C/T]ATCTGCCAATCTCTG	672511
rs27015117	snp	A/G	0.132653	0.220748	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119471909	CTAACTTGTGCCTCA[A/G]ACACTATTGTCCTTC	672511
rs27015118	snp	A/G	0.336735	0.234472	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119471848	CTGGGAATCAGCCCT[A/G]GACATCAGCACTGCT	672511
rs27015119	snp	A/G	0.124444	0.216185	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119471675	GCAGGGTTGTTACAC[A/G]GCAGCTCTTATGCAT	672511
rs27015120	snp	C/T	0.124444	0.216185	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119471597	TTAGGAGTGTCCACC[C/T]TGTCCCCATATCACT	672511
rs27015121	snp	A/G	0.5	0	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119471105	GCCTGCTAAGCAGCA[A/G]GCTACCAGGCTGCAG	672511
rs27015122	snp	A/G	0.244898	0.249948	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119470752	CTTCTAGGGAGGTGC[A/G]AAGGCTGTGTCATAC	672511
rs27015123	snp	C/T	0.459184	0.136902	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119470050	ATCCTTGAGGCTGCA[C/T]AGTCAATGCCCTCCT	672511
rs27015124	snp	C/T	0.124444	0.216185	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119469709	TACAGTCTGGGTGGC[C/T]CTCCAATGGAGAGGC	672511
rs27015125	snp	C/T	0.152778	0.230321	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119469190	GAGTCCTAAGCACTG[C/T]GTTAGTCAGGCTTCT	672511
rs27015126	snp	A/G	0.375	0.216506	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119468225	ACTACTAAAGCATAA[A/G]CTATGAGATTCTACT	672511
rs27015127	snp	A/G	0.152778	0.230321	synonymous-codon, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119468029	GGCCTTGTACACAGA[A/G]GTGGCTGCTTTGTAC	672511
rs27015128	snp	A/G	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119467683	TGATACTGATGTCAA[A/G]GTTTTTAGACGTCTG	672511
rs27015129	snp	C/G	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119467527	TAGTGGCTGGAACGG[C/G]TGCAATGACACTTGA	672511
rs27015130	snp	A/G	0.444444	0.157135	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119467476	GACACTGTACTAGAA[A/G]TCAGACTTTCATGGT	672511
rs27015131	snp	A/G	0.497041	0.0383476	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119467428	TTACATACATCAAAT[A/G]ATGGAGTGAGCAACT	672511
rs27015132	snp	A/C	0.297521	0.245442	missense, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119467227	CTGCTCCAATTGCAG[A/C]AGGACCACGTAAGCC	672511
rs27015133	snp	A/G	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119467119	GGCTCTGTCTCAGAA[A/G]TCCTTCCAAGTCTCT	672511
rs27015134	snp	A/G	0.375	0.216506	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119467032	GCAAGTAACTATAAA[A/G]TCTGTACAGGCCCTT	672511
rs27015135	snp	A/G	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119466997	CTCCTGGCCTCAATC[A/G]AGTGCTGTGAATGGA	672511
rs27015136	snp	C/T	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119466985	CAAATTTTATGTCTC[C/T]TGGCCTCAATCAAGT	672511
rs27015137	snp	A/G	0.32	0.24	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119466867	TTCCTGGTACTCAGA[A/G]CTCACTTCTTCCTGT	672511
rs27015138	snp	C/T	0.345679	0.230967	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119466855	ACTGTAGCACCTTTC[C/T]TGGTACTCAGAGCTC	672511
rs27015139	snp	A/C	0.345679	0.230967	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119466832	AGAAGTGTGGCTTTT[A/C]AGGCCTCACTGTAGC	672511
rs27015140	snp	A/G	0.277778	0.248452	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119466746	TGTTTCTGCCCTACC[A/G]GCAATTGTGTCCTTT	672511
rs27015141	snp	C/T	0.165289	0.235211	missense, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119466244	GCTGAAGACAAGCGG[C/T]GCTTCCTGAAGCATG	672511
rs27015142	snp	A/T	0.297521	0.245442	missense, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119466234	CACAGAACTGGCTGA[A/T]GACAAGCGGCGCTTC	672511
rs27015143	snp	C/G	0.165289	0.235211	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119466184	GTCTTCATAGCAGGT[C/G]TCTGTCACTGTCCCT	672511
rs27015144	snp	C/T	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119465870	ATGCCTTAGTCTCTA[C/T]GCCCTCATTCCTCAG	672511
rs27015145	snp	C/G	0.396694	0.202437	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119465852	GCTTGCTGGTGTGAA[C/G]TAATGCCTTAGTCTC	672511
rs27015146	snp	A/C	0.5	0	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119465574	CTCATCACTGTGGAC[A/C]CTTTCAATCACCCTT	672511
rs27015147	snp	A/G	0.165289	0.235211	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119464921	GGCTGCAGCGTGCCG[A/G]ACACAGACCCGGCCT	672511
rs27015148	snp	C/T	0.165289	0.235211	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119464914	GTGCTGGGGCTGCAG[C/T]GTGCCGGACACAGAC	672511
rs27015149	snp	C/T	0.165289	0.235211	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119464623	TGCAGGAACACAGAA[C/T]TGGGCCTGCTGGCAC	672511
rs27015150	snp	A/G	0.297521	0.245442	intron-variant	Rnf213	Mm_Celera	11:119464303	TGGCCTGTGTTTTTT[A/G]AATGTGGGCAGGGTC	672511
rs27015151	snp	A/G	0.375	0.216506	missense	Rnf213	GRCm38.p3	11:119463609	TCTCCATTTGATGAT[A/G]TTGTTGACCAGACTC	672511
rs27015152	snp	C/T	0.197531	0.244432	intron-variant	Rnf213	Mm_Celera	11:119463537	CTTTGTACCATGATA[C/T]GAACTATAGTCCCCT	672511
rs27015153	snp	A/C	0.497041	0.0383476	synonymous-codon	Rnf213	GRCm38.p3	11:119463415	TGAGAAGAGTGTCAT[A/C]GATACACTGCTGTCC	672511
rs27015154	snp	C/T	0.297521	0.245442	intron-variant	Rnf213	Mm_Celera	11:119463261	AAGTATTGGGCAACA[C/T]ATTCTACAATTCTTC	672511
rs27015155	snp	C/T	0.297521	0.245442	intron-variant	Rnf213	Mm_Celera	11:119462776	TCTGCCTGGCTTAGC[C/T]GCCAGTGAGGCCTAG	672511
rs27015156	snp	A/G	0.396694	0.202437	intron-variant	Rnf213	Mm_Celera	11:119462605	TGAGATTCAGCTTGT[A/G]CCCTGCCACTCATCC	672511
rs27015157	snp	G/T	0.21875	0.248039	intron-variant	Rnf213	Mm_Celera	11:119462399	TGGTTTCAGAGAACT[G/T]CCATAAGTAATGCCA	672511
rs27015158	snp	A/C	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119460979	CGTGGCTGGTTCCCA[A/C]TACTTGGCTGGAAGG	672511
rs27015159	snp	A/G	0.124444	0.216185	intron-variant	Rnf213	Mm_Celera	11:119460965	AGTCTCATCTTTACC[A/G]TGGCTGGTTCCCAAT	672511
rs27015160	snp	A/G	0.345679	0.230967	intron-variant	Rnf213	Mm_Celera	11:119460892	GACACCTTCTACCTG[A/G]TAATCTTAGGATGCT	672511
rs27015161	snp	C/G	0.297521	0.245442	intron-variant	Rnf213	Mm_Celera	11:119460283	ATTCAGTTGCAGGAA[C/G]AGGTATGCAGTTAAC	672511
rs27015162	snp	G/T	0.336735	0.234472	missense	Rnf213	Mm_Celera	11:119460010	GGGGACTGAGAGCCA[G/T]ATTCCTGAGCTGAGT	672511
rs27015163	snp	C/T	0.32	0.24	intron-variant	Rnf213	Mm_Celera	11:119459198	TGGGGAAGGGGCAGG[C/T]TGTCAAGGTCAGGAG	672511
rs27015164	snp	A/G	0.142012	0.225474	synonymous-codon	Rnf213	Mm_Celera	11:119458837	GAAGAATCTGTCCAC[A/G]CCACTGGAGCTCGTC	672511
rs27015165	snp	A/G	0.132653	0.220748	intron-variant	Rnf213	Mm_Celera	11:119458671	AACGCACTGGGACTC[A/G]GGATTCAGGGCGTCT	672511
rs27015166	snp	A/G	0.244898	0.249948	intron-variant	Rnf213	Mm_Celera	11:119458630	AAGTAACGGAGCAGT[A/G]AATAGTTCTCGAGCC	672511
rs27015167	snp	C/T	0.486111	0.0821678	synonymous-codon	Rnf213	GRCm38.p3	11:119447238	TTTGCTAAACAGGTA[C/T]ACTGCCATCAATGAA	672511
rs27030168	snp	C/T	0.497041	0.0383476	intron-variant	Rnf213	GRCm38.p3	11:119447192	CCAGCCAGCTCCTAA[C/T]ATGGGTTTGTTTGCA	672511
rs27030169	snp	C/G	0.152778	0.230321	intron-variant	Rnf213	Mm_Celera	11:119446945	CAGTTTTCCACCACT[C/G]TGCTACAATGATAGC	672511
rs27030170	snp	A/G	0.260355	0.249785	intron-variant	Rnf213	Mm_Celera	11:119446266	TCACACACAGCCTCA[A/G]AAAAAACTCTTCCCA	672511
rs27030171	snp	A/T	0.5	0	intron-variant	Rnf213	GRCm38.p3	11:119446216	GCCAAGTATGTTTTC[A/T]GTGCTTGTCCAGAAA	672511
rs27030172	snp	G/T	0.444444	0.157135	intron-variant	Rnf213	GRCm38.p3	11:119446209	AGCCTCTGCCAAGTA[G/T]GTTTTCTGTGCTTGT	672511
rs27030173	snp	C/T	0.473373	0.11227	missense	Rnf213	GRCm38.p3	11:119446175	ACTTTGACGATGGCA[C/T]CCGTAGCGCGCAGCT	672511
rs27030174	snp	C/T	0.486111	0.0821678	intron-variant	Rnf213	GRCm38.p3	11:119446089	GAACTCACCCACTAA[C/T]CTATTCCCTTTCTCC	672511
rs27030175	snp	A/G	0.495868	0.0452663	intron-variant	Rnf213	GRCm38.p3	11:119446031	TGTGGCCCTGGCCTC[A/G]CCCATGCCTCAAGGA	672511
rs27030176	snp	G/T	0.244898	0.249948	intron-variant	Rnf213	Mm_Celera	11:119445886	GTTGTGGGTCGTGTC[G/T]AGGCGTCCCGCTCTG	672511
rs27030177	snp	C/T	0.142012	0.225474	intron-variant	Rnf213	Mm_Celera	11:119445816	CACCCTTGTCAGGTG[C/T]GTTGGCAGAGCTGTA	672511
rs27030178	snp	A/G	0.473373	0.11227	intron-variant	Rnf213	GRCm38.p3	11:119445792	CTGCTAGCTCCATTC[A/G]TTAGGGCTCACCCTT	672511
rs27030179	snp	C/T	0.336735	0.234472	intron-variant	Rnf213	Mm_Celera	11:119445622	AACGCTCATCTCCCT[C/T]TTTGCAGATCACCAC	672511
rs27030180	snp	C/G	0.456747	0.140554	intron-variant	Rnf213	GRCm38.p3	11:119444984	CTGCTCAGCAACACT[C/G]AAAGTTTAGGAACGA	672511
rs27030181	snp	C/G	0.18	0.24	intron-variant	Rnf213	Mm_Celera	11:119444944	ACAGGGCACTCACTG[C/G]TTCCCTCCTAACTGC	672511
rs27030182	snp	C/T	0.398438	0.258522	intron-variant	Rnf213	GRCm38.p3	11:119444942	GGACAGGGCACTCAC[C/T]GGTTCCCTCCTAACT	672511
rs27030183	snp	A/G	0.244898	0.249948	intron-variant	Rnf213	Mm_Celera	11:119444344	GAAGGCTTCAGGGTC[A/G]GTATAGCCAGAGCAG	672511
rs27030184	snp	A/C	0.152778	0.230321	intron-variant	Rnf213	Mm_Celera	11:119444310	GAGACAGAAGGCTGC[A/C]ATGGAAATAGACCAG	672511
rs27030185	snp	C/T	0.260355	0.249785	intron-variant	Rnf213	Mm_Celera	11:119443981	CCAGTGTGCGTGTAG[C/T]TTAGAAAGGCAGCAT	672511
rs27030186	snp	A/G	0.244898	0.249948	synonymous-codon	Rnf213	Mm_Celera	11:119443110	GAACATTAACCGGGT[A/G]AAGATTTGCATGGAG	672511
rs27030187	snp	C/T	0.132653	0.220748	synonymous-codon	Rnf213	Mm_Celera	11:119442552	CATCTTTGTGTCCCG[C/T]GGCAGTCCCAACGAG	672511
rs27030188	snp	A/G	0.260355	0.249785	synonymous-codon	Rnf213	Mm_Celera	11:119442381	GGTGGTGTTGGATGA[A/G]GTTGGGCTGGCTGAA	672511
rs27030189	snp	C/T	0.132653	0.220748	synonymous-codon	Rnf213	Mm_Celera	11:119442165	GGGGAAGCCCGGCAG[C/T]TCCAAATCCCTTGCC	672511
rs27030190	snp	A/G	0.456747	0.140554	missense	Rnf213	GRCm38.p3	11:119441675	TCTCTGTGAATCCCA[A/G]TGAGACTTGTGTGAT	672511
rs27030191	snp	C/T	0.244898	0.249948	synonymous-codon	Rnf213	Mm_Celera	11:119441544	GCGGCAGCTGGTCTA[C/T]CGTGTTCATGCTCTG	672511
rs27030192	snp	A/C	0.244898	0.249948	missense	Rnf213	Mm_Celera	11:119440407	ATTTCAGTATGAAAA[A/C]GGCTCTGTGGAAGGC	672511
rs27030193	snp	A/G	0.142012	0.225474	intron-variant	Rnf213	Mm_Celera	11:119440064	TCTAAACCCTTAGCA[A/G]GCAAAAGTTTCCAGT	672511
rs27030194	snp	G/T	0.260355	0.249785	intron-variant	Rnf213	Mm_Celera	11:119439844	TTGGTATCCAAGTGT[G/T]CAGGGAAGGCGTATT	672511
rs27030195	snp	A/G	0.142012	0.225474	intron-variant	Rnf213	Mm_Celera	11:119439840	CTTGTTGGTATCCAA[A/G]TGTTCAGGGAAGGCG	672511
rs27030196	snp	A/G	0.132653	0.220748	intron-variant	Rnf213	Mm_Celera	11:119439772	ATAAGCCTAAGGTGC[A/G]TAGATGTTAGTAAAT	672511
rs27030197	snp	A/G	0.486111	0.0821678	intron-variant	Rnf213	Mm_Celera	11:119439183	GAAGATTAGTGTCCT[A/G]ACCAGGTTTGTTAGA	672511
rs27030198	snp	C/T	0.489796	0.070696	missense	Rnf213	Mm_Celera	11:119438060	ATATGGCGTCGGAGC[C/T]CGGGTCATTTATACC	672511
rs27030199	snp	A/G	0.142012	0.225474	synonymous-codon	Rnf213	Mm_Celera	11:119437751	AAGCGCACTGCTGCC[A/G]TTCTTGAAGGAGAAA	672511
rs27030200	snp	C/T	0.132653	0.220748	intron-variant	Rnf213	Mm_Celera	11:119437429	TTGCGCCGTCAGTAG[C/T]CAGGAAAAGGGCAAA	672511
rs27030201	snp	C/T	0.497778	0.0332592	intron-variant	Rnf213	GRCm38.p3	11:119437331	GCTGTTTGTTTCCTT[C/T]CATCCTGTCCTCTCT	672511
rs27030202	snp	C/G	0.152778	0.230321	intron-variant	Rnf213	Mm_Celera	11:119437121	CCTTCTCTAGCAAGG[C/G]TGACTCTGATGAAGC	672511
rs27030203	snp	A/G	0.152778	0.230321	intron-variant	Rnf213	Mm_Celera	11:119437118	CTTCCTTCTCTAGCA[A/G]GGCTGACTCTGATGA	672511
rs27030204	snp	G/T	0.429688	0.173817	synonymous-codon	Rnf213	GRCm38.p3	11:119436585	CTTGTGTGGCCACTC[G/T]GAGGTGTTGCCAGCT	672511
rs27030205	snp	C/T	0.444444	0.157135	synonymous-codon	Rnf213	Mm_Celera	11:119436579	CCTGATCTTGTGTGG[C/T]CACTCGGAGGTGTTG	672511
rs27030206	snp	A/G	0.444444	0.157135	missense	Rnf213	GRCm38.p3	11:119436397	GAGCCCAGCCTAATG[A/G]GCAAGCTTCAGGTTA	672511
rs27030207	snp	A/G	0.277778	0.248452	missense	Rnf213	GRCm38.p3	11:119436308	TCGTACAAGCTACCA[A/G]TGCCTGTGAAAGCAA	672511
rs27030208	snp	A/G	0.142012	0.225474	missense	Rnf213	Mm_Celera	11:119436295	ACTGTCCAGGACCTC[A/G]TACAAGCTACCAGTG	672511
rs27030209	snp	A/G	0.32	0.24	intron-variant	Rnf213	GRCm38.p3	11:119435356	TGTGGAGAAGAGATG[A/G]CCAACAGATATTCTT	672511
rs27030210	snp	A/G	0.429688	0.173817	synonymous-codon	Rnf213	GRCm38.p3	11:119435022	CTCCACAGAGGAACT[A/G]AAGGAACTTTTAAAT	672511
rs27030211	snp	A/T	0.244898	0.249948	intron-variant	Rnf213	Mm_Celera	11:119434430	TTTCTCTCTCATCAC[A/T]AATAAACCCAGATGC	672511
rs27030212	snp	C/T	0.46875	0.121031	intron-variant	Rnf213	GRCm38.p3	11:119434361	CTTGAGGCTCCCTAA[C/T]GCTCGTTCTGTTATT	672511
rs27030213	snp	C/T	0.396694	0.202437	intron-variant	Rnf213	GRCm38.p3	11:119433911	GTCATCCTCAGAAAT[C/T]GTAAACGACCATTAA	672511
rs27030214	snp	C/G	0.152778	0.230321	intron-variant	Rnf213	Mm_Celera	11:119433833	GGATGGCTGGAAGGA[C/G]CATGCCTATGAAAAG	672511
rs27030215	snp	A/G	0.444444	0.157135	intron-variant	Rnf213	GRCm38.p3	11:119433755	ATTGTGCGTGGGAAT[A/G]TGTGCTCTCTCTTGA	672511
rs27030216	snp	C/T	0.142012	0.225474	intron-variant	Rnf213	Mm_Celera	11:119433340	CAAGACCTTGGTGTC[C/T]GGTTATAGTTTCACT	672511
rs27030217	snp	A/G	0.277778	0.248452	intron-variant	Rnf213	Mm_Celera	11:119433187	CTATGTTTAAGTGAT[A/G]TTACGTAGTCAAGAC	672511
rs27030218	snp	C/T	0.142012	0.225474	intron-variant	Rnf213	Mm_Celera	11:119431869	CATGTTTTACTCAGA[C/T]GGTGTCTCGCTCCTT	672511
rs27030219	snp	C/G	0.42	0.183303	missense	Rnf213	Mm_Celera	11:119431730	AGACGGAGCTTGTTG[C/G]CTGGCTGCACAAGGC	672511
rs27030220	snp	C/T	0.35503	0.226867	synonymous-codon	Rnf213	Mm_Celera	11:119431695	GCCTCGCCAGCGCTG[C/T]TTGGAGGAGCTTGCC	672511
rs27030221	snp	A/G	0.5	0	intron-variant	Rnf213	GRCm38.p3	11:119431386	CTATGGTGAGAAACA[A/G]ATTTCAAAGACCATG	672511
rs27030222	snp	C/T	0.49827	0.0293608	synonymous-codon	Rnf213	GRCm38.p3	11:119430713	AGCTTTGGGTGTGAC[C/T]GGTGACTTCAGTGTT	672511
rs27030223	snp	C/T	0.142012	0.225474	missense	Rnf213	Mm_Celera	11:119430397	CTCTGGATAAGGACC[C/T]CAGAGAGTTGAAGGT	672511
rs27030224	snp	C/T	0.297521	0.245442	synonymous-codon	Rnf213	Mm_Celera	11:119430384	GAGTCACTGAATACT[C/T]TGGATAAGGACCCCA	672511
rs27030225	snp	A/G	0.473373	0.11227	intron-variant	Rnf213	GRCm38.p3	11:119429722	TGTTTGTTTTCTTAG[A/G]GAAGCAGCTAGAGGA	672511
rs27030226	snp	A/G	0.142012	0.225474	intron-variant	Rnf213	Mm_Celera	11:119429692	AGGAAAGATGCCCAT[A/G]TTCTGCAGTGGTTGT	672511
rs27030227	snp	A/G	0.5	0	intron-variant	Rnf213	GRCm38.p3	11:119429033	AAGAGACAGACAGCC[A/G]ACCTGCAGTCTCAGT	672511
rs27030228	snp	C/T	0.297521	0.245442	intron-variant	Rnf213	Mm_Celera	11:119429001	CTGGCAGACACAGCT[C/T]ATCTACCTTGCTGAG	672511
rs27030229	snp	A/G	0.444444	0.157135	intron-variant	Rnf213	Mm_Celera	11:119428961	GCCCTCTTCCCTTGC[A/G]CGTCCCCGCCCTCTT	672511
rs27030230	snp	C/T	0.495868	0.0452663	intron-variant	Rnf213	Mm_Celera	11:119428958	CCCGCCCTCTTCCCT[C/T]GCGCGTCCCCGCCCT	672511
rs27030231	snp	A/G	0.260355	0.249785	missense	Rnf213	Mm_Celera	11:119428055	AGGCCTGTGATGTGA[A/G]GAGCTTGCTGAAAAG	672511
rs27030232	snp	C/G	0.260355	0.249785	intron-variant	Rnf213	Mm_Celera	11:119427426	AGCGCCGCCGGAGCA[C/G]GAGGAGTCATCAGGG	672511
rs27030233	snp	A/G	0.260355	0.249785	intron-variant	Rnf213	Mm_Celera	11:119427382	GAGTAGCAGTGCACC[A/G]GTCAAGTGCTGTCTC	672511
rs27030234	snp	C/T	0.297521	0.245442	intron-variant	Rnf213	Mm_Celera	11:119427323	ATCTAAGTTGTAAGT[C/T]TCACAGAGATGGGGA	672511
rs27030235	snp	C/T	0.35503	0.226867	intron-variant	Rnf213	Mm_Celera	11:119426875	GCTTTTATCATAGAG[C/T]TGCTGCAGTTTCTTG	672511
rs27030236	snp	A/T	0.142012	0.225474	intron-variant	Rnf213	Mm_Celera	11:119426809	TGGACAGCACTCACA[A/T]TCGAAGCTCCTCCTG	672511
rs27030237	snp	C/T	0.142012	0.225474	intron-variant	Rnf213	Mm_Celera	11:119426759	TTATGGAACCATTAA[C/T]GTGTGTGGACTTAGA	672511
rs27030238	snp	C/T	0.459184	0.136902	intron-variant	Rnf213	GRCm38.p3	11:119426718	CAAGGATCTGTGGCC[C/T]TCCTCTTTATTCTCT	672511
rs27030239	snp	A/G	0.260355	0.249785	intron-variant	Rnf213	Mm_Celera	11:119426314	TCACGGTAAGGTGCT[A/G]GGTTAGGCACTAAAA	672511
rs27030240	snp	C/T	0.142012	0.225474	synonymous-codon	Rnf213	Mm_Celera	11:119426109	GGAGCCTGTGTTTGA[C/T]GTGGATGAGATCTTC	672511
rs27030241	snp	A/C	0.297521	0.245442	intron-variant	Rnf213	Mm_Celera	11:119425837	CTCAGTTAGCCTGGG[A/C]TTGGCCTTGCTTTTT	672511
rs27030242	snp	G/T	0.297521	0.245442	intron-variant	Rnf213	Mm_Celera	11:119425742	ACAGCCGGCTTCCTA[G/T]CCTCTTCTGTAACTA	672511
rs27030243	snp	A/G	0.244898	0.249948	intron-variant	Rnf213	Mm_Celera	11:119425679	GTCTGCAGTCAGCGC[A/G]GAATGGCTGCAGGCC	672511
rs27030244	snp	A/G	0.345679	0.230967	intron-variant	Rnf213	Mm_Celera	11:119425648	GCAGCTCTAGAGTAA[A/G]CAACTCAGTGGACTT	672511
rs27030245	snp	A/G	0.429688	0.173817	intron-variant	Rnf213	GRCm38.p3	11:119425030	CCAGGATCATTTGTC[A/G]GAGAGATTGTGCTGT	672511
rs27030246	snp	C/T	0.297521	0.245442	intron-variant	Rnf213	Mm_Celera	11:119425011	TATGTGGAGAGCTAG[C/T]TTCCCAGGATCATTT	672511
rs27030247	snp	C/T	0.152778	0.230321	intron-variant	Rnf213	Mm_Celera	11:119424888	TGCCGGGTTGCGTTC[C/T]TTTCTGTTAATTCTT	672511
rs27030248	snp	A/G	0.260355	0.249785	intron-variant	Rnf213	Mm_Celera	11:119424360	CCTGCTTGTTCTGAG[A/G]CCCTACTGCATTGGC	672511
rs27030249	snp	A/C	0.142012	0.225474	missense	Rnf213	Mm_Celera	11:119424276	GTGAGCTCTGCCTGC[A/C]AGGTCACTAGCCTTT	672511
rs27030250	snp	C/T	0.35503	0.226867	synonymous-codon	Rnf213	GRCm38.p3	11:119424206	CAGTCAGTGTCGTGA[C/T]GGAGGACTCCATGAC	672511
rs27030251	snp	C/T	0.444444	0.157135	synonymous-codon	Rnf213	GRCm38.p3	11:119424176	TCCCCGTTTGCAGAT[C/T]TCCTTCTTCTGCAGC	672511
rs27030252	snp	A/G	0.152778	0.230321	missense	Rnf213	Mm_Celera	11:119423029	CGGCTGGTGGAGATC[A/G]GCTTCCCAGAGAAGC	672511
rs27030253	snp	C/T	0.297521	0.245442	intron-variant	Rnf213	Mm_Celera	11:119422761	GTGACAGTGAGGATC[C/T]GAGAGCCGTATTGTT	672511
rs27030254	snp	C/T	0.152778	0.230321	intron-variant	Rnf213	Mm_Celera	11:119421966	AAGGCTCATCCCGAG[C/T]TGGCAAAAGGAAACG	672511
rs27030255	snp	A/G	0.260355	0.249785	intron-variant	Rnf213	Mm_Celera	11:119421680	CCTTTGCTGTGAGGT[A/G]ATGGAGATACAGTGT	672511
rs27030256	snp	C/T	0.297521	0.245442	intron-variant	Rnf213	Mm_Celera	11:119421309	TCCCTCTCTTGTGTC[C/T]ACAGCATACTGACGA	672511
rs27030257	snp	C/T	0.46875	0.121031	missense	Rnf213	Mm_Celera	11:119420101	TACAGATCTACTTGA[C/T]TGAGTGTTTGACCCT	672511
rs27030258	snp	A/G	0.132653	0.220748	intron-variant	Rnf213	Mm_Celera	11:119419448	TTCACGGTACTTCCC[A/G]AGTCCTGGCTTCCAT	672511
rs27030259	snp	C/T	0.486111	0.0821678	intron-variant	Rnf213	GRCm38.p3	11:119419258	CAAAGGCAGCTTTGT[C/T]TTCCACACAGCTCTG	672511
rs27030260	snp	A/C	0.497041	0.0383476	intron-variant	Rnf213	GRCm38.p3	11:119419102	TGTCCAGAGGCCTTT[A/C]TTTTCTTGGCTCAAT	672511
rs27030261	snp	A/G	0.46875	0.121031	missense	Rnf213	GRCm38.p3	11:119418153	CGCTCCTGGCTCAGC[A/G]TGGTCCCTCTTGAAA	672511
rs27030262	snp	A/G	0.32	0.24	intron-variant	Rnf213	GRCm38.p3	11:119417994	ACTTTCGTTTCCCAC[A/G]AAGCATTGCAACCCT	672511
rs27030263	snp	C/T	0.244898	0.249948	intron-variant	Rnf213	Mm_Celera	11:119417808	CCTGATGCAGGCTGA[C/T]CACAGCGACAGGGAT	672511
rs27030264	snp	G/T	0.297521	0.245442	synonymous-codon	Rnf213	Mm_Celera	11:119416642	GGACAAAGCACCCAC[G/T]AGGTAAGCTGAAGAG	672511
rs27030265	snp	A/C	0.260355	0.249785	intron-variant	Rnf213	Mm_Celera	11:119416234	ATTCTCTCAGCTGTG[A/C]AGTGTAGGAGAGGAC	672511
rs27030266	snp	C/T	0.473373	0.11227	intron-variant	Rnf213	GRCm38.p3	11:119415992	GCGTCTCAGCGTCCA[C/T]GGAAGCCGGGATGGG	672511
rs27030267	snp	C/T	0.489796	0.070696	missense	Rnf213	GRCm38.p3	11:119415214	AAAAGGACCTGGATT[C/T]GCTGTGCTATCTCCT	672511
rs27030268	snp	A/G	0.473373	0.11227	missense	Rnf213	GRCm38.p3	11:119415199	AATTTACTGTACCCA[A/G]AAAGGACCTGGATTC	672511
rs27030269	snp	C/T	0.277778	0.248452	intron-variant	Rnf213	Mm_Celera	11:119414863	CTAGGATACCACCTC[C/T]GCACATTCCCGAGCT	672511
rs27030270	snp	G/T	0.408163	0.193609	intron-variant	Rnf213	Mm_Celera	11:119414766	AGGGGTTTCCTCTGT[G/T]CACCGCCTCCAGGAT	672511
rs27030271	snp	G/T	0.5	0	missense	Rnf213	GRCm38.p3	11:119414530	TCATGACTCAATTCC[G/T]GCAGTTTTACTCGGT	672511
rs27030272	snp	G/T	0.277778	0.248452	missense	Rnf213	GRCm38.p3	11:119414378	GAGGTCCACTGGGTT[G/T]TTCCAGCAAGCCAAG	672511
rs27030273	snp	A/T	0.297521	0.245442	intron-variant	Rnf213	GRCm38.p3	11:119413790	CTTACCTGGGCAGAC[A/T]CTCAGCTAGGTCAGA	672511
rs27030274	snp	C/T	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119413647	GATTTAGAGCTCACT[C/T]ATGTAAAATGAATGA	672511
rs27030275	snp	A/C	0.32	0.24	intron-variant	Rnf213	GRCm38.p3	11:119413106	AAGGATACAAAACTA[A/C]ACTTCCCTTTGTCCT	672511
rs27030276	snp	A/T	0.5	0	intron-variant	Rnf213	Mm_Celera	11:119412374	TTCTCAGTGCTGACA[A/T]TGGAACTCAGGGTCT	672511
rs27030277	snp	A/T	0.48	0.0979796	intron-variant	Rnf213	GRCm38.p3	11:119412039	GTCCCTGTGTTCTTC[A/T]GCCTTGCACCCATGT	672511
rs27030278	snp	G/T	0.42	0.183303	intron-variant	Rnf213	GRCm38.p3	11:119410891	CAGTGAGTATCTAGG[G/T]ATTGGAGCTGCCGCT	672511
rs27030279	snp	C/T	0.244898	0.249948	missense	Rnf213	Mm_Celera	11:119410735	AGTGCGTTTAACCCA[C/T]GGGATACAGTCACTG	672511
rs27030280	snp	C/G	0.408163	0.193609	missense	Rnf213	GRCm38.p3	11:119409515	CCTGTAGCCTCCAAG[C/G]ACGGAGACCAGGTAG	672511
rs27030281	snp	C/G	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119407074	CTCATCCTGCACAGC[C/G]CAATCCTAGCTTGGC	672511
rs27030282	snp	C/T	0.48	0.0979796	intron-variant	Rnf213	Mm_Celera	11:119406756	GGGCTAACATTTGTC[C/T]TAGGGATACCACTAG	672511
rs27030283	snp	C/T	0.408163	0.193609	intron-variant	Rnf213	Mm_Celera	11:119406734	CTCTCTGTACCCATC[C/T]GCCTCAGGGCTAACA	672511
rs27030284	snp	C/T	0.408163	0.193609	intron-variant	Rnf213	Mm_Celera	11:119406175	GGAATCTGCTCCGTG[C/T]CACTGCTGAGTCCTT	672511
rs27030285	snp	A/C	0.408163	0.193609	intron-variant	Rnf213	Mm_Celera	11:119406146	ACTGGGCAGCCGGCT[A/C]GAACTGGCTAAAGGG	672511
rs27030286	snp	A/G	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119405529	TGTAAGGAGGTGGCT[A/G]CGACTAGACCTTCAC	672511
rs27030287	snp	C/T	0.444444	0.157135	intron-variant	Rnf213	Mm_Celera	11:119405464	GTGTCCCTATACCTC[C/T]TGCCATTGGCCATGG	672511
rs27030288	snp	A/C	0.408163	0.193609	intron-variant	Rnf213	GRCm38.p3	11:119404974	CTGTCTGGTGATTGG[A/C]TTGTGAGGCCCTTTG	672511
rs27030289	snp	A/G	0.493827	0.0552116	missense	Rnf213	GRCm38.p3	11:119402542	CTCAAGAACGACAAT[A/G]CCTTGGTGGTGTCAT	672511
rs27030290	snp	C/G/T	0.473373	0.11227	intron-variant	Rnf213	GRCm38.p3	11:119394478	AAATCAGGATGTGCA[C/G/T]GGCGCTAGCCTAGGG	672511
rs27030291	snp	G/T	0.277778	0.248452	intron-variant	Rnf213	Mm_Celera	11:119391069	TCTAGTCCAGGCTTC[G/T]CAGTTTCCTGAGCAG	672511
rs27030292	snp	A/G	0.152778	0.230321	upstream-variant-2KB, intron-variant	Mir1932, Rnf213	GRCm38.p3	11:119390376	GTGGGCCGGCGGCTC[A/G]TGGCCCCTGTGGTCA	672511
rs27030293	snp	A/G	0.277778	0.248452	upstream-variant-2KB, intron-variant	Mir1932, Rnf213	Mm_Celera	11:119390338	GATGCTGTTTCATTG[A/G]GTGCCGGTCCTGCTA	672511
rs27030294	snp	C/T	0.244898	0.249948	upstream-variant-2KB, utr-variant-5-prime	Mir1932, Rnf213	GRCm38.p3	11:119389988	AGCGGCTGTAGTCGC[C/T]CTGGACAAGCGAGCT	672511
rs27030295	snp	C/T	0.444444	0.157135	upstream-variant-2KB, utr-variant-5-prime	Mir1932, Rnf213	GRCm38.p3	11:119389867	GTCTGGGGCTAGAGG[C/T]TTGAACCTATCAATG	672511
rs27030296	snp	A/G	0.297521	0.245442	upstream-variant-2KB, utr-variant-5-prime	Mir1932, Rnf213	Mm_Celera	11:119389773	GCAACCTGTAGGTGA[A/G]CACTCTTGCTGTCCT	672511
rs27030297	snp	A/C	0.277778	0.248452	upstream-variant-2KB	Rnf213	Mm_Celera	11:119387813	CTTTGCTGTTACTAA[A/C]GCTGATTGCACAACA	672511
rs27030298	snp	C/T	0.277778	0.248452	upstream-variant-2KB	Rnf213	Mm_Celera	11:119387753	ACCCCAGTGTGGTAG[C/T]GTGGCTCTAACAGGC	672511
rs29384406	snp	C/T	0.444444	0.157135	intron-variant	Rnf213	GRCm38.p3	11:119400246	TGGGAAGGAAAAATT[C/T]GACTTCCAAGGATTC	672511
rs29387298	snp	A/G	0.444444	0.157135	synonymous-codon	Rnf213	GRCm38.p3	11:119416510	ATGTGACCGTTGGCT[A/G]GGTATCTTACCCCTC	672511
rs29387325	snp	A/G	0.5	0	intron-variant	Rnf213	Mm_Celera	11:119396259	ACAGGCTGAGGCAAG[A/G]TCCGAGGAGGAATCG	672511
rs29388577	snp	A/C	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119463126	AACAACAAAAAAAAA[A/C]CAGAGCCTAGTTTTA	672511
rs29388937	snp	C/G	0.32	0.24	intron-variant	Rnf213	GRCm38.p3	11:119435290	TGAAGTAGGGTAGAC[C/G]CTATGAGCAGCAGGT	672511
rs29389259	snp	A/G	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119430035	GAGAGCCAGTGCTAC[A/G]CAGAAAATCTGTCTC	672511
rs29390295	snp	A/C/T	0.375	0.216506	synonymous-codon	Rnf213	GRCm38.p3	11:119430242	AGCCGTGATTAAGCT[A/C/T]CCCAATTCCTCCTCC	672511
rs29391068	snp	A/G	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119398326	CAGGCTGCAGGCTCA[A/G]TGGGGCAGCTGGGTC	672511
rs29391667	snp	G/T	0.32	0.24	intron-variant	Rnf213	GRCm38.p3	11:119417636	CATGTTGTGCTGTGG[G/T]GCATCATGGTGAACC	672511
rs29394620	snp	C/T	0.32	0.24	missense	Rnf213	GRCm38.p3	11:119430520	TTGCTGAAGTTGATG[C/T]CATCTTCAAAGACTT	672511
rs29394994	snp	A/G	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119449623	TTTAACCACCACCCA[A/G]GGCCACATGATTGCT	672511
rs29396404	snp	A/G	0.32	0.24	intron-variant	Rnf213	GRCm38.p3	11:119417562	CACGACCCCTGCCAT[A/G]ATGCCCAGGGTACCA	672511
rs29397191	snp	A/G	0.444444	0.157135	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119485964	ACCACTGGCCTGGCT[A/G]TGATGTTACAAAAAC	672511
rs29397232	snp	G/T	0.444444	0.157135	intron-variant	Rnf213	GRCm38.p3	11:119424064	ACTTGCACAGTATGT[G/T]TGCTCACAGAGACAG	672511
rs29398181	snp	C/T	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119409631	AACCTGTCATGACAG[C/T]CCAGTGTTTACGAGG	672511
rs29398199	snp	C/T	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119447768	AACACACCAGCCTTA[C/T]CTTCATTCCCCTTTG	672511
rs29398338	snp	C/T	0.375	0.216506	synonymous-codon	Rnf213	GRCm38.p3	11:119430293	CTGCCTGAGCCCTGA[C/T]ATCCGAGAAATGGCA	672511
rs29399167	snp	C/T	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119431802	TTGCCTGGGTCCTGC[C/T]AGCGGCACCAGCTGG	672511
rs29399794	snp	C/T	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119449518	TGTAAGGGAATCAAC[C/T]CCTCTTAAGTTACCC	672511
rs29400573	snp	A/G	0.444444	0.157135	intron-variant	Rnf213	GRCm38.p3	11:119437246	TTTCTTTCCTCTGGG[A/G]GTGCTGCTGGCTTCT	672511
rs29401722	snp	A/C	0.444444	0.157135	intron-variant	Rnf213	GRCm38.p3	11:119450952	CCATCTGGGAGCCAG[A/C]TCTGTATTGGCCTTT	672511
rs29401772	snp	C/G	0.444444	0.157135	intron-variant	Rnf213	GRCm38.p3	11:119448066	AGACTTCGGGGTACT[C/G]ATCACTCTTTTAGCA	672511
rs29402396	snp	A/T	0.32	0.24	utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119486763	TCACCGGACAGAGAG[A/T]GGAGAAGGATGAGCG	672511
rs29404702	snp	A/G	0.444444	0.157135	intron-variant	Rnf213	GRCm38.p3	11:119464590	ACATGGAGTTGTCCT[A/G]AGTTAGGTCAACTCA	672511
rs29404997	snp	C/T	0.444444	0.157135	intron-variant	Rnf213	Mm_Celera	11:119439557	ACCTGGGGCCGGAAC[C/T]TGAAAGACATCAAAG	672511
rs29406043	snp	C/T	0.32	0.24	intron-variant	Rnf213	GRCm38.p3	11:119435289	CTGAAGTAGGGTAGA[C/T]CCTATGAGCAGCAGG	672511
rs29406496	snp	C/T	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119448340	AGGCGTGGTGGCGCA[C/T]CTCTTTAATCCCAGC	672511
rs29406945	snp	C/T	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119400709	GCTGGAGAGATGGCT[C/T]AGCAGTCAAGAGCAC	672511
rs29407894	snp	A/G	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119462948	CTTCAGGAGACAGAG[A/G]AGCAGGGCCTCAGCA	672511
rs29408749	snp	G/T	0.375	0.216506	synonymous-codon	Rnf213	GRCm38.p3	11:119408923	GGAGGATGGCTTCGT[G/T]CACACTGAGGGCAGC	672511
rs29409815	snp	A/G	0.444444	0.157135	synonymous-codon	Rnf213	GRCm38.p3	11:119416495	GTGCATAGACGAGAG[A/G]TGTGACCGTTGGCTG	672511
rs29410251	snp	A/G	0.375	0.216506	missense	Rnf213	GRCm38.p3	11:119449277	GAGACAAGCCAGTCA[A/G]AGGAATTGGCAGAGG	672511
rs29410259	snp	A/G	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119448122	GGGGGCTGGAGAGTT[A/G]GATTCAGAGATTAAG	672511
rs29410410	snp	A/G	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119449077	TAGAGCCCAGGCTAG[A/G]GGATGCCTGAGCCTG	672511
rs29411065	snp	C/T	0.5	0	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119484500	CATGGTGGCTCACAA[C/T]CACCCGTAATGAGAT	672511
rs29411947	snp	A/G	0.444444	0.157135	intron-variant	Rnf213	Mm_Celera	11:119422380	TCTGTAGACCAGGCT[A/G]GCCTCAAACTCAGAA	672511
rs29412264	snp	C/T	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119416824	ACATTTCAGTGCCAA[C/T]GACAACACGGGTGCT	672511
rs29412384	snp	C/G	0.32	0.24	intron-variant	Rnf213	Mm_Celera	11:119400662	AAATGTGTGGGGAAA[C/G]AAGGTCAAATAGGAA	672511
rs29413982	snp	C/T	0.375	0.216506	missense	Rnf213	GRCm38.p3	11:119449812	AGAATGAGAGCTGTG[C/T]GCGCAACATGAGAAG	672511
rs29415165	snp	G/T	0.375	0.216506	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119467909	GAAATGTAGTTCAGT[G/T]TAAGGGCCTGATAAG	672511
rs29416057	snp	G/T	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119429414	CAGAAGAGGGTGTCA[G/T]ATCCCATTATGGATG	672511
rs29416206	snp	A/G	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119400690	GAAAGGTAAGACCTC[A/G]GGGGCTGGAGAGATG	672511
rs29416316	snp	A/C	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119431035	TCCTTGCTCTCTTTT[A/C]AATTCATGGCCTCTT	672511
rs29419578	snp	C/T	0.375	0.216506	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119481547	TCTTTGGACTGTCTG[C/T]ACCTCAGTCCCCTGG	672511
rs29421729	snp	C/G	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119414130	CCTCCCAAGTGCTGG[C/G]ATTAAAGGCATGCAC	672511
rs29422391	snp	A/G	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119412288	TGTGTTGGGAGGGCA[A/G]GGGAGACAGGTGGAG	672511
rs29424827	snp	A/G	0.375	0.216506	synonymous-codon	Rnf213	GRCm38.p3	11:119408806	TCTGGACATGCCTCC[A/G]AGTCCTGGATCTCAC	672511
rs29426020	snp	C/G	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119416277	CTGCTCTGGGGATTC[C/G]TTGAGGGTTGCTTTA	672511
rs29426880	snp	C/T	0.5	0	intron-variant	Rnf213	GRCm38.p3	11:119400146	GCCATAGATAAACAC[C/T]TTACATGATCCCCCA	672511
rs29427863	snp	A/G	0.444444	0.157135	intron-variant	Rnf213	GRCm38.p3	11:119412224	TGTGTGTGTGAGTGC[A/G]TGTGTGTGCACACGT	672511
rs29429703	snp	G/T	0.444444	0.157135	intron-variant	Rnf213	Mm_Celera	11:119395098	AAAGACACAGATGGG[G/T]TTCCTTTGGGGTCCC	672511
rs29430244	snp	C/T	0.32	0.24	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119467039	ACTATAAAATCTGTA[C/T]AGGCCCTTTCTAGGC	672511
rs29430271	snp	A/C	0.32	0.24	synonymous-codon	Rnf213	GRCm38.p3	11:119436081	GAAGGGAGATGTCAT[A/C]CAGCTCCTGGGAGCC	672511
rs29430355	snp	G/T	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119429233	TTGCCCTTAATGGAT[G/T]CAATGTAAATCAGGT	672511
rs29430979	snp	A/C	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119407413	TGGGAATGACTCTGA[A/C]CTTGTAATCCTCCTG	672511
rs29431093	snp	A/T	0.32	0.24	intron-variant	Rnf213	GRCm38.p3	11:119434914	TGCAGGAACTAACTT[A/T]TAAATGTGTGCTGCC	672511
rs29431644	snp	C/T	0.32	0.24	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119478179	ATCCCACCTATAAGC[C/T]AGCTTCTTTAAGCTC	672511
rs29431750	snp	C/T	0.444444	0.157135	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119482370	TTTTTTTCTATTTTA[C/T]CTCTAAAACTTTCTC	672511
rs29433394	snp	A/G	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119463223	ACCAAAATACTATCC[A/G]AATATCCCTTCCCTC	672511
rs29433885	snp	A/G	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119409271	GTCTCCACACTCCCT[A/G]GGACTTGCTCCTTGG	672511
rs29434215	snp	A/T	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119448222	GGATCTGATGTCTTC[A/T]TCTGACCTACAAGGA	672511
rs29435997	snp	G/T	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119417116	GCATCAAATCTATAC[G/T]TTTTTCTTTTGCGAG	672511
rs29438045	snp	C/T	0.375	0.216506	utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119487093	GAGAGTACCTGTCCT[C/T]CGATGTCTGCATCCC	672511
rs29438567	snp	C/T	0.375	0.216506	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119485787	GTGAGTTCCAGGACA[C/T]CCAGGGATACACAGA	672511
rs29439453	snp	G/T	0.375	0.216506	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119485674	TTTATCATGTCTCGG[G/T]TTATAAAACAGCCCT	672511
rs29441149	snp	C/T	0.444444	0.157135	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119464821	TATCGCGTATTTTTT[C/T]CCCAGTACATTCTAT	672511
rs29442692	snp	C/T	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119448342	GCGTGGTGGCGCATC[C/T]CTTTAATCCCAGCAC	672511
rs29442775	snp	A/C	0.32	0.24	intron-variant, nc-transcript-variant	Rnf213, LOC102639982	GRCm38.p3	11:119478061	TTCCTCAATCTGTCG[A/C]TCGACAGATGGGCTG	672511
rs29442777	snp	C/T	0.32	0.24	intron-variant	Rnf213	GRCm38.p3	11:119435242	TGGGTCTGCAGGATG[C/T]AGTACCCCGATTCAC	672511
rs29442843	snp	C/T	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119430140	TGAGATAAATAACCC[C/T]CACCCTTTAATTCTG	672511
rs29443613	snp	C/T	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119416832	GTGCCAACGACAACA[C/T]GGGTGCTTTGTGTGC	672511
rs29444176	snp	A/C	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119453354	AGGGGACGGGCAGAA[A/C]GGGCACAGAAGGCCT	672511
rs29446055	snp	A/G	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119444943	GACAGGGCACTCACT[A/G]GTTCCCTCCTAACTG	672511
rs29446148	snp	A/G	0.32	0.24	intron-variant	Rnf213	GRCm38.p3	11:119435261	ACCCCGATTCACAAC[A/G]CCAGAGACATATCTG	672511
rs29446538	snp	C/T	0.375	0.216506	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119485628	TTTCCTTATAAAGCG[C/T]CTACAGAGAAGACTA	672511
rs29446782	snp	C/T	0.444444	0.157135	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	GRCm38.p3	11:119464693	GGTAGTTGCTACCAA[C/T]GATACAGTTTAAATA	672511
rs29449697	snp	A/C	0.375	0.216506	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119485641	CGTCTACAGAGAAGA[A/C]TACAAGCAAGAGTCT	672511
rs29450070	snp	A/G	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119413862	AGCCATACCCTCCAG[A/G]CCCATAGCTCCTCGT	672511
rs29451771	snp	C/T	0.32	0.24	synonymous-codon	Rnf213	GRCm38.p3	11:119442951	CAGGGGCCTGGACGG[C/T]GCTGAGTCCCGTTAC	672511
rs29452369	snp	A/G/T	0.32	0.24	intron-variant	Rnf213	GRCm38.p3	11:119445361	CTGGTTTATAAGAAG[A/G/T]GGCATTTGTGGTGAG	672511
rs29452489	snp	G/T	0.32	0.24	intron-variant	Rnf213	Mm_Celera	11:119401009	TCAGGGGGAGGTATT[G/T]AAAAATGCCATCCAG	672511
rs29452829	snp	A/G	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119407599	CAGCCCTGGCTGCTG[A/G]TCCTTAGGCCAACAA	672511
rs29453035	snp	A/G	0.444444	0.157135	intron-variant	Rnf213	GRCm38.p3	11:119399136	CCCTAGGGAGAAAGA[A/G]GGGAAGGAACCGAGT	672511
rs29453507	snp	C/G	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119448341	GGCGTGGTGGCGCAT[C/G]TCTTTAATCCCAGCA	672511
rs29456796	snp	C/T	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119449365	GTGACGTGAGTCCGG[C/T]TTTTGCCATTAGCTA	672511
rs29457038	snp	A/G	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119402070	CCAACCACAGAAGGT[A/G]CAGATCAGAAGAGAT	672511
rs29458008	snp	A/G	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119416805	CCAGAGCTGGGGGTG[A/G]CGTACATTTCAGTGC	672511
rs29458078	snp	C/T	0.444444	0.157135	synonymous-codon	Rnf213	GRCm38.p3	11:119416513	TGACCGTTGGCTGGG[C/T]ATCTTACCCCTCCTG	672511
rs29458574	snp	A/G	0.32	0.24	intron-variant, nc-transcript-variant	Rnf213, LOC102639982	GRCm38.p3	11:119478064	CTCAATCTGTCGCTC[A/G]ACAGATGGGCTGAGA	672511
rs29462861	snp	A/C	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119431264	TAGGTGGTGGCTGGC[A/C]TTGAACTCACAGAGA	672511
rs29463342	snp	A/G	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119395433	CCATGGGCTGAAGGA[A/G]GCCAGCCTGGTTTGA	672511
rs29464591	snp	A/G	0.32	0.24	intron-variant	Rnf213	GRCm38.p3	11:119417228	AAGCCTTGACACTAA[A/G]TAGAACTTAGAAGAA	672511
rs29465752	snp	C/T	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119409613	TGTCAGCATGGCTTC[C/T]TCAACCTGTCATGAC	672511
rs29467245	snp	C/T	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119463166	ATTAGGAGGCTGATA[C/T]AGAATTGTGGAGTTC	672511
rs29467595	snp	A/G	0.375	0.216506	missense	Rnf213	GRCm38.p3	11:119449331	GAGGAGATGAAAAAG[A/G]CCTCTGACCCAAGAA	672511
rs29470853	snp	G/T	0.32	0.24	intron-variant	Rnf213	GRCm38.p3	11:119430784	TGCTGAGGGGTGAGG[G/T]CTTGGGTTGGGTAGG	672511
rs29470861	snp	A/C	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119429264	TATCCTCAAATTCAC[A/C]CAGATCCACCTACCT	672511
rs29473365	snp	A/G	0.32	0.24	synonymous-codon	Rnf213	GRCm38.p3	11:119441286	GGCCCAGCACAAGCT[A/G]GATACCATCTTGTTC	672511
rs29473642	snp	A/T	0.375	0.216506	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119474903	GATGGCATTAGTTTT[A/T]AAAAAAGATTAATTT	672511
rs29473839	snp	C/G	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119411918	GGCTTTGAAGGTGCC[C/G]TTTCAGAGAAGGGCC	672511
rs29474535	snp	A/T	0.375	0.216506	missense	Rnf213	GRCm38.p3	11:119408898	CCCTGGACACAGAGA[A/T]CATGCCAATGGAGGA	672511
rs29475110	snp	A/C	0.375	0.216506	synonymous-codon	Rnf213	GRCm38.p3	11:119430254	GCTCCCCAATTCCTC[A/C]TCCTACAAAAGGGAG	672511
rs29476378	snp	A/G	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119429627	ACTTTTTACTCAGTT[A/G]TGTACCCAGTTTCCT	672511
rs29478196	snp	C/T	0.375	0.216506	intron-variant	Rnf213	Mm_Celera	11:119448098	TGGTGCAATTAAAAA[C/T]CCAGGTTAGGGGGCT	672511
rs29479530	snp	C/T	0.32	0.24	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119480283	TGTTCCCCTCCATGG[C/T]CTGCTCTTATAGAGC	672511
rs29481470	snp	C/G	0.5	0	intron-variant	Rnf213	GRCm38.p3	11:119396394	TCTTACTGATTTTCC[C/G]ATTCACTGAGAGAGG	672511
rs29483114	snp	G/T	0.444444	0.157135	intron-variant	Rnf213	Mm_Celera	11:119396053	TGCTAAGGCAAACAC[G/T]CGAAAGGACATGAGA	672511
rs29484564	snp	G/T	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119416421	TGGGCCATCCTCCCC[G/T]CACCGACTCCTTCAT	672511
rs29484689	snp	C/T	0.5	0	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119484505	TGGCTCACAATCACC[C/T]GTAATGAGATCTGAC	672511
rs29485936	snp	A/G	0.375	0.216506	intron-variant	Rnf213	GRCm38.p3	11:119448611	TCCACACACGTGCAC[A/G]TGGGTGCACACATAC	672511
rs29486917	snp	A/C	0.32	0.24	intron-variant	Rnf213	GRCm38.p3	11:119417184	CTGGTAAGTTTATGG[A/C]AGTGGGGGTAGAATT	672511
rs33881733	snp	G/T	0.444444	0.157135	intron-variant	Rnf213	GRCm38.p3	11:119464529	TGCCTCTATTCTATG[G/T]GGACCCACCAGCTGC	672511
rs45852983	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119474969	CCAGAAGAGAGAATC[C/T]GAGCCCATTACAAGT	672511
rs45892383	snp	G/T			intron-variant	Rnf213	GRCm38.p3	11:119446427	TCATGTGGAAGCTGG[G/T]TGTGGCGATGCACAC	672511
rs46094580	snp	C/T			intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119484535	CGGCCTCTTCTGGTG[C/T]GTCTGAAGACAGCTA	672511
rs46139804	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119422876	GTCCAGGTCAGCCTC[A/G]AGCTCTTGGACTTCA	672511
rs46174607	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119416098	ACCCCCCTCCCCCTC[A/G]AGCACAGTGACCCCA	672511
rs46317948	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119446255	GGAACCAACACTCAC[A/G]CACAGCCTCAGAAAA	672511
rs46591095	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119427938	CCCTGGCATGGAGCA[C/T]GTTCAGAGAGAGGCA	672511
rs46623852	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119446555	AAATCAAGAAGGGCT[A/G]CTCCTAAGGAAAGAT	672511
rs46726092	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119446309	ATGTCATGAACAACA[C/T]GTTAACAAGAATATT	672511
rs46766676	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119393753	CCCAGAACCCACAAA[A/G]TGGCTTCCAGCCTCT	672511
rs46864886	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119397064	ATTCTCACCTCTGGG[A/G]CACCACGTGTGAATG	672511
rs46898729	snp	A/G			intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119484536	GGCCTCTTCTGGTGT[A/G]TCTGAAGACAGCTAC	672511
rs47105082	snp	G/T			intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119475517	AGTCTCTCTTGTTAT[G/T]GCTGCTACTCTGCAT	672511
rs47258239	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119446460	CAATGCTGGGGAGGC[A/G]GAGCCATATGATCCT	672511
rs47437361	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119444575	GGGGTGGAGAAATGG[C/T]TTAACAGGTAGGAGC	672511
rs47726509	snp	C/G			intron-variant	Rnf213	GRCm38.p3	11:119397200	AGAGAATGTGTCCCT[C/G]AGAGGGAATGGGGTG	672511
rs47768276	snp	C/T			synonymous-codon	Rnf213	GRCm38.p3	11:119414411	CCGCATCCTCGATAG[C/T]ACAAGAAAGGAACTG	672511
rs47787756	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119446374	GAAAAAGCTAGAGTT[C/T]TAGAGGCTAGCAAGA	672511
rs47816842	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119417113	AAGGCATCAAATCTA[C/T]ACTTTTTTCTTTTGC	672511
rs48103957	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119397471	CTGCCTCTGCCTCCC[A/G]AGTGCTGGGATTAAA	672511
rs48168383	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119444581	GAGAAATGGCTTAAC[A/G]GGTAGGAGCACTGGC	672511
rs48355634	snp	C/G			intron-variant	Rnf213	GRCm38.p3	11:119444566	GAATGTTTAGGGGTG[C/G]AGAAATGGCTTAACA	672511
rs48515784	snp	G/T			intron-variant	Rnf213	GRCm38.p3	11:119444568	ATGTTTAGGGGTGGA[G/T]AAATGGCTTAACAGG	672511
rs48750033	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119447493	TTCTTACCCAGTCAC[A/G]GTTAGCTGTGTATGG	672511
rs48795606	snp	A/G			intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119484964	AAATGGGGCATGGTG[A/G]CACATACCTATAATC	672511
rs48865087	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119396286	ATCGTGATGTCTGGA[A/G]GGAGTGTAAAAAAGG	672511
rs49422403	snp	A/T			synonymous-codon, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119481284	ACAAGAGTTTGATCT[A/T]GAGAAGATCCAACGG	672511
rs49485569	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119435905	TCATGGTTCCCTTTC[C/T]CCCAGGTCTTCAGCA	672511
rs49532120	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119444673	TAACACTAGTTCCAG[A/G]GGATTCAATGCTTTC	672511
rs49932641	snp	G/T			intron-variant	Rnf213	GRCm38.p3	11:119433288	CAGATTCAATATATG[G/T]TCAGTGTTCTTAGCA	672511
rs50042663	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119415685	TAGCTGTGGAGCCTT[C/T]TCTCCAGCCCCAGTA	672511
rs50060792	snp	A/G			intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119475524	CTTGTTATGGCTGCT[A/G]CTCTGCATATTCAAG	672511
rs50203152	snp	C/T			synonymous-codon	Rnf213	GRCm38.p3	11:119449735	TCAGTGTTCACAGTT[C/T]CTAGATACCACCAGA	672511
rs50371454	snp	A/T			intron-variant	Rnf213	GRCm38.p3	11:119447491	ATTTCTTACCCAGTC[A/T]CAGTTAGCTGTGTAT	672511
rs50590886	snp	G/T			intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119474640	GCAAACCTATTGTGT[G/T]GGAGACACATGCCAA	672511
rs50686853	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119446473	GCGGAGCCATATGAT[C/T]CTTGGGGACAGTGAC	672511
rs50722163	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119431782	TGGCCAGCCCGTGCA[C/T]GGGCTTGCCTGGGTC	672511
rs51002610	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119398055	CATTGTGGTGGGAAG[C/T]ATGGCAGCGTGCAGG	672511
rs51176930	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119403846	GCAGATCTACCGCTA[C/T]ACTACCACCTTCCAC	672511
rs51190426	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119398064	GGGAAGTATGGCAGC[A/G]TGCAGGCAGACAACT	672511
rs51253289	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119445223	CAGGGGTCACGTATC[C/T]GATTTGTAACAGAAT	672511
rs51812500	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119414325	ACCCATCCTTCTGTC[C/T]CCTCAGACTGGCATC	672511
rs52046127	snp	A/C/G			intron-variant	Rnf213	GRCm38.p3	11:119447507	CAGTTAGCTGTGTAT[A/C/G]GTGGTTGCACATACT	672511
rs52283718	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119435668	AAAAAAAAAAAAAAA[A/C]AAAAACAAAAAAAAC	672511
rs52292907	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119410687	CATGTGTGCATGCAC[C/T]CTGGCAGCCAGTGTT	672511
rs52464696	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119468547	AACTCTTTTTGCTTC[C/T]TTTTTTTTTTTTTTT	672511
rs107801412	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119455475	AGGTTATTCATCTCA[A/G]GCTCCTAGATAACAC	672511
rs107849735	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119435674	AAAAAAAAAAAAAAA[A/C]AAAAAAAACAAAAAG	672511
rs107889848	snp	G/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476031	GAAAGCCTGGTTTTT[G/T]TTTTTTTTTTTTTTT	672511
rs107894051	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119435677	AAAAAAAAAAAACAA[A/C]AAAAACAAAAAGAGA	672511
rs108132013	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119455141	GCTCAGCCTCTCCTA[G/T]CTCATCTGTCTTCTA	672511
rs108395638	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119435683	AAAAAACAAAAAAAA[A/C]AAAAAGAGAAAAAGA	672511
rs108829774	snp	G/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119468569	TTTTTTTTTTTTTTT[G/T]GGTTTTTTGAGACAG	672511
rs108887146	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119412078	GAACCCTTGCTAAAT[C/T]CCTTTCTTCTCCCTC	672511
rs211762289	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119433822	GCCTCAGGGAAGGAT[A/G]GCTGGAAGGACCATG	672511
rs211763968	snp	A/C			intron-variant	Rnf213	GRCm38.p3	11:119445850	AGAACTGGTTAATGA[A/C]CTGGAAGGCTGAGTC	672511
rs211833629	snp	A/G			missense	Rnf213	GRCm38.p3	11:119436016	TACTGTTGCCCTGAC[A/G]GGGGCATCTTCATGA	672511
rs211836694	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119427266	AAATCCCAGAGATTC[A/G]CCTGCTTCTGCGAGT	672511
rs211854155	in-del	-/A			intron-variant	Rnf213	Mm_Celera	11:119428603	CATTTGCCAGAGGTT[-/A]ATCAGTCTGACTTTT	672511
rs211868850	snp	C/T			utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119487195	CAGCTCAGCCCCACA[C/T]GTCTTGCTGTAAGGC	672511
rs211871464	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119434576	GTGCTGGGGGTGGGG[C/G]ATAGACAGACACTTC	672511
rs211897007	snp	C/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119472116	TGACTTGGGAGGACA[C/G]TCAGGTCCAACACAC	672511
rs211944358	snp	A/T			missense	Rnf213	GRCm38.p3	11:119414400	CAAGCCAAGAACCGC[A/T]TCCTCGATAGTACAA	672511
rs211947263	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119427923	GCTCCCTCCACATGG[C/T]CCTGGCATGGAGCAC	672511
rs211953607	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119478969	TACCCAGTCTTAATG[A/G]GATTGTTAGGCTATT	672511
rs212002293	snp	A/C			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119479811	AGAGCTGCTATGAGT[A/C]GGAACATGGCTGTAT	672511
rs212020769	in-del	-/TT			intron-variant	Rnf213	Mm_Celera	11:119456915	TGGGGGTTGAATCTG[-/TT]CTCGGGCTGGAGAGA	672511
rs212021851	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473331	GAAGATTAGCCTCTT[C/T]TAATGTTCACCTAGT	672511
rs212022848	in-del	-/C			intron-variant	Rnf213	Mm_Celera	11:119420965	GCTAGCGGACTTTTT[-/C]ACTGTCTTTTCACTG	672511
rs212024339	snp	C/T			intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119464794	AGATCCATGGTGATA[C/T]TAAGGACTCTATATC	672511
rs212025330	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119415018	CCTCCATGTTCACAC[A/G]TCCTTCCCTCCTGGG	672511
rs212091495	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119472549	TAAACGGCACACAAT[C/T]AAGCTTGCCAAATAT	672511
rs212092533	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119455139	CAGCTCAGCCTCTCC[G/T]AGCTCATCTGTCTTC	672511
rs212106832	snp	A/G			upstream-variant-2KB, intron-variant	Mir1932, Rnf213	Mm_Celera	11:119390387	GCTCATGGCCCCTGT[A/G]GTCACAGTCCCTGAA	672511
rs212112826	snp	C/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119465348	GGTATATAGTCATGA[C/G]TTGCCTGATGGTGTC	672511
rs212148307	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119404020	TTTATCTGCCCAATC[A/G]TCAGCTCTCCTGTAT	672511
rs212201158	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	Mir1932, Rnf213	Mm_Celera	11:119389473	CCAAACAAAAAGACA[C/T]AGGTAGGAGGATCAG	672511
rs212205665	in-del	-/AAAAA			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119465264	AGAAAACAAACAAAC[-/AAAAA]AAAAAAAACAAAGTT	672511
rs212209187	in-del	-/A			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119484352	CTTTATGATTAAAAG[-/A]AAAAAAAAAAGTCAG	672511
rs212381805	snp	A/G			synonymous-codon	Rnf213	GRCm38.p3	11:119437640	TCTCTACGTGAACAC[A/G]CTGCATACAAAACTA	672511
rs212413965	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119447094	TGGGATGTGAGCCCA[C/T]TTCATCCTAAGGGTG	672511
rs212455513	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119429196	GGGGCAGGCCTGGTG[A/G]CTGAGCCCTTGTGTA	672511
rs212456309	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119482217	CACTGTTTCTAAAGA[C/T]GGCATCTTCAGCATA	672511
rs212471026	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119418596	GTTTGCCTGAGTTTA[C/T]CAATAGCTTTTTCAA	672511
rs212494649	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119428774	CTGTGCCTCTTCCCT[C/T]GCACGTCCCCGCCCT	672511
rs212494694	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119438178	GGTTAAGCACTCCTA[G/T]CCCACACTATTTATT	672511
rs212522007	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119455752	CAGGTCTGCATCTGC[C/T]GTCTTTCCTGAGGGA	672511
rs212634224	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119392496	CTGGGGGGGGGGGGG[A/G]GAGACAGTGTGAAAC	672511
rs212647206	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119467369	GACGGGTCTGGGCTT[C/T]TCTCTTATACCAGAA	672511
rs212647563	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475144	CTCTGTGTAGCCCTG[A/G]CTGTCCTGGAACTCA	672511
rs212654999	in-del	-/AGAGAC			intron-variant	Rnf213	Mm_Celera	11:119431330	AAGAGAGACAGGCAG[-/AGAGAC]AGAGACAGAGATGGA	672511
rs212745910	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119457377	CCGAACAGTGGTGGC[A/G]CACACCTTTAATCCC	672511
rs212757953	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119449161	GGGACAAGAAGCCTG[A/G]CAAGTCCCACTCTGG	672511
rs212791503	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119394000	AGCCTTGCTGGCTCA[A/G]TGTAGAGGAAGCCCT	672511
rs212801627	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119474575	TGTTCTCAAATCACC[A/G]TGCACAAGGTCCTGT	672511
rs212814847	snp	C/G			intron-variant	Rnf213	GRCm38.p3	11:119406310	GCCCCCGAGTCCACA[C/G]CCACGTACCCATCAT	672511
rs212872634	in-del	-/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119470007	CCAGATCTAACCAGA[-/T]TGACAGCCAAGACTA	672511
rs212875741	snp	G/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119481582	ATTCTCCAGTCTCTA[G/T]GGGACTTAGCATTTG	672511
rs212919656	in-del	-/A			intron-variant	Rnf213	Mm_Celera	11:119440007	CCTTGATTGTGTTAG[-/A]AAAATGCATCTTTGT	672511
rs212921847	snp	A/G			missense	Rnf213	Mm_Celera	11:119440315	CCTGCCATGGACCCA[A/G]TGGAGTTCTGCAGTG	672511
rs213043997	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119421250	ATGGGTTCTGGGGAT[C/G]AGACTCAGGTCTTCT	672511
rs213081858	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119430914	GGTTTCAGGCCATCC[A/G]TCGGGGGATCAGTAG	672511
rs213128721	snp	A/G			missense, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119483933	GAGGCAGGCCTAGAC[A/G]CCTTCCTCCTGGAGC	672511
rs213165158	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119439352	AGGTCCATCCCCTTA[C/T]GAAAACACATGAGGC	672511
rs213169567	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119423345	GTCATGATGGAGATC[C/G]TAGTCATATACAGGG	672511
rs213199031	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119396531	AAACTCTACTGGACT[A/G]GACTGCTGGTCTGCC	672511
rs213232740	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119460456	GAAACCCCTATGCTT[C/T]TGCCCCTCCACACCT	672511
rs213232782	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119469878	GGCAAAGGAGCACAA[A/G]GAGCTCTCCCTGGAC	672511
rs213289168	snp	C/G			intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119469177	CAGTGGTGGTACAGA[C/G]TCCTAAGCACTGTGT	672511
rs213291787	in-del	-/T			intron-variant	Rnf213	Mm_Celera	11:119397521	GCCCCACAGCAACTC[-/T]TTTTTTTTTTTAATT	672511
rs213310768	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119461134	TAAAAGATTCAGAAA[A/G]TAGCCAACACAAAGA	672511
rs213505817	snp	A/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119483301	CCTGTTGGAAAGTGT[A/T]GCATGGGAATCAGCA	672511
rs213531286	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119485438	AGGCGGGTGCTGAGA[A/G]TCATTCCCAAGCTCT	672511
rs213536160	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119451537	TTGTTTCCAGCTTTC[A/G]CCTCACACCTTGGTC	672511
rs213537998	in-del	-/TTT			intron-variant	Rnf213	Mm_Celera	11:119453538	ATTTTTTTCTTTTTC[-/TTT]TTTTTTTTTTTTAAA	672511
rs213546248	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119432687	AGGAGTCAGATCCCT[C/T]TGAGCAGGAGGTATA	672511
rs213576568	in-del	-/TT			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119481378	AACTAGCTAATGTGC[-/TT]AGTTATGTCAAAAGT	672511
rs213597045	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119408503	TCTTGCAGAGGACCC[A/G]GGCTCAATTCCCAGC	672511
rs213610648	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119426608	TGTTGGCACACTTTG[A/G]TCAAGTCGGGGTTCG	672511
rs213648088	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119433361	TAGTTTCACTTACAA[C/T]TACTGCCCAAAACTC	672511
rs213655005	in-del	-/ATAC			intron-variant	Rnf213	Mm_Celera	11:119395949	GTTTTGCTAGGGCAA[-/ATAC]ATGAGGGAGTGTTTT	672511
rs213765444	in-del	-/GGG			intron-variant	Rnf213	Mm_Celera	11:119434487	GGCTTCTGGAGCAGT[-/GGG]GGAAGCCTGACTGGT	672511
rs213793531	snp	A/T			intron-variant	Rnf213	Mm_Celera	11:119450772	ACACCAGGAGAGTAC[A/T]TTATTGTCTATGGTT	672511
rs213831310	in-del	-/T			intron-variant	Rnf213	Mm_Celera	11:119444729	AGCATCCGCCCCCCC[-/T]CCCCAACATGCAGCA	672511
rs213858469	snp	A/T			missense	Rnf213	Mm_Celera	11:119462215	GCTCATCCCTGGGCA[A/T]ATGATGTGCCCCTAC	672511
rs213869893	snp	A/T			intron-variant	Rnf213	Mm_Celera	11:119397533	ACTCTTTTTTTTTTT[A/T]ATTTTTTTTTTAATT	672511
rs213870285	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119413349	TATTTTTTTTAAGAT[C/T]GGCCTTGGCCGTATA	672511
rs213889363	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119453902	GTTTATGTAGCTGTT[C/T]ACAGAGGTAAGAACA	672511
rs213893747	snp	A/C			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119478173	GTTACTATCCCACCT[A/C]TAAGCCAGCTTCTTT	672511
rs213950797	snp	A/G			upstream-variant-2KB	Rnf213	Mm_Celera	11:119387931	GGCCCCTGTATTTGC[A/G]GTTCTGAGCTGCAGT	672511
rs214029691	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119454961	ACAATAACCAATTTT[C/T]TTAACTCCCTACCAG	672511
rs214069078	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119445217	CTTTCACAGGGGTCA[C/T]GTATCCGATTTGTAA	672511
rs214117316	in-del	-/TTAA			intron-variant	Rnf213	Mm_Celera	11:119453734	GCTCCAGACCTGTAT[-/TTAA]TTTTTTAAATTTTAT	672511
rs214141287	in-del	-/C			intron-variant	Rnf213	Mm_Celera	11:119424856	TCTGCCTCAGTTACA[-/C]CCCCCACGAGCCGCA	672511
rs214156538	in-del	-/ACAC			intron-variant	Rnf213	Mm_Celera	11:119423432	TGGAGGGACGGACGG[-/ACAC]ACACACACACACACA	672511
rs214173465	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119428708	AGGGCACCTCATGAG[C/T]ACTAGGTCGGTCAGG	672511
rs214214660	snp	A/G			missense	Rnf213	Mm_Celera	11:119434793	ATCAACAGCAGGGGC[A/G]TCTACGTTATTGAGG	672511
rs214252822	snp	C/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119478787	TTCTCCACTTCCTGG[C/G]CCCCATTTGACACTG	672511
rs214257397	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119414148	TAAAGGCATGCACCA[C/G]CACCGCCCGGCAGGC	672511
rs214280609	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119416184	TCAGGCGGCCTTCCC[C/T]GGGCAGCCCTTGCAT	672511
rs214299956	snp	A/C			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119480662	ATGGCCATGTCTGTG[A/C]GCCTCTTCTTCCCCT	672511
rs214341531	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119456081	CAGCCTGGATAATGG[C/T]TCCTTTTTGTGGCAG	672511
rs214364496	in-del	-/TTT			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119484311	AGCAGGCTTCTTTGG[-/TTT]TTTGTATTCTATTTG	672511
rs214376614	in-del	-/GCACTTAGTACATACCAA			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119482804	TCTGGAGTGCTGCCT[-/GCACTTAGTACATACCAA]GCATCAGGCTAGTGC	672511
rs214377649	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119400985	AAAAGGGGTGAAATG[A/G]AAGATGCTTCAGGGG	672511
rs214448361	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119456761	CCACCTGGGGATGGA[A/C]ACAGTCTTCGATGCC	672511
rs214463678	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119471865	ACATCAGCACTGCTT[A/G]TACTCTTTCTTTTTT	672511
rs214520883	in-del	-/A			intron-variant	Rnf213	Mm_Celera	11:119425942	TGTTTCTCTCATTTC[-/A]AAAACTAATAAGACA	672511
rs214544837	snp	C/G			missense, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119479867	TCTGCTCAACAGATG[C/G]GCTGAGAAAGCTGTT	672511
rs214565418	in-del	-/T			intron-variant	Rnf213	Mm_Celera	11:119461219	ATTTAAAATGTTTTA[-/T]TTTTTCAATTATTTT	672511
rs214603952	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119448162	TAGAGGACCTGCCTA[A/C]ACCCATGTGTTGGAT	672511
rs214615696	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119481722	TAACGGCCATGGCAT[A/G]CCTGTCATTTTAGCC	672511
rs214626327	snp	C/T			missense	Rnf213	GRCm38.p3	11:119402618	AGGAGGTCCTACTCT[C/T]GTCCACAGACCCAGG	672511
rs214647082	in-del	-/C			intron-variant	Rnf213	Mm_Celera	11:119391230	CTTTCTCCTCCTCCG[-/C]CCCCCCCATTTTGTT	672511
rs214718945	snp	C/G			missense, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119466265	CTGAAGCATGTTGAG[C/G]AGTTCTGCACACGCG	672511
rs214762506	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119418691	TGAGACACACAGAGA[A/G]CATGGATCTATCAGG	672511
rs214841162	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119408290	TAGTGCACGGGTGTC[A/G]TGTTTGGGAAGCCTG	672511
rs214881676	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119407620	AGGCCAACAACTCAC[C/T]CTGTAAGGTGCCTGT	672511
rs214884032	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119391271	TTGTTTGTTTGTTTG[G/T]TTTTTTGGCCTTCAA	672511
rs214940765	snp	C/T			synonymous-codon	Rnf213	Mm_Celera	11:119458762	TGCAGCAATGGCCTG[C/T]GCTGAAATGCTCAAG	672511
rs214948401	snp	A/G			missense, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473405	GCCACGTGTTGGGGA[A/G]CCCACAGTCCAGTGG	672511
rs214950161	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119404296	GGCAGTGCGCAGGCA[C/G]ACATGGTGCTGGAGG	672511
rs214977190	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119457625	TGCCAACCATTAAAA[C/G]AGCATTATCTGAGTT	672511
rs215082792	snp	C/T			nc-transcript-variant, intron-variant	Mir1932, Rnf213	Mm_Celera	11:119390514	AGTCTCCGACCCCAT[C/T]AACTCTCGGGTTGCG	672511
rs215089790	snp	A/C/T			intron-variant	Rnf213	Mm_Celera	11:119439200	CCAGGTTTGTTAGAA[A/C/T]TAGAACCGGGAGGAA	672511
rs215109477	in-del	-/CC			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119467094	AACTCCCAAAGATGG[-/CC]CCCCCGCGGGCTCTG	672511
rs215159314	in-del	-/AT			intron-variant	Rnf213	Mm_Celera	11:119435238	CCATGGGTCTGCAGG[-/AT]ATGTAGTACCCCGAT	672511
rs215174948	snp	G/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119465448	TGTCTGCACAGCAGA[G/T]GGCCCCAGTGATGCA	672511
rs215199541	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119450344	TGATTCTTAGAGATG[C/T]ACTCCTGGTGGTATT	672511
rs215211399	snp	G/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119484225	AACTCAACTCACTCT[G/T]TAGATCAGGCTAGAT	672511
rs215216499	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119429930	TTCCCCTACACTAAG[A/G]AGGAGAGGTGACGCC	672511
rs215299876	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119438389	GCTGAGCAAACCATG[A/G]TGAGCTGACCAGTAA	672511
rs215340656	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119425237	ATGTGTGCCTGCATG[A/C]ATGCCAGCCATGGCA	672511
rs215345526	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119409691	ATGGAGCTCCCATGC[C/T]AGAGAGAAGCAGGAA	672511
rs215380907	snp	A/T			intron-variant	Rnf213	Mm_Celera	11:119423782	ATTTTTTATATTATA[A/T]TGAATGTTTTATCCA	672511
rs215387532	snp	C/G			intron-variant	Rnf213	GRCm38.p3	11:119395465	TGTGACCTGGCTTCA[C/G]TGGCGGCCACCCTAT	672511
rs215395360	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476643	CTTTACCCATCATCG[C/T]TGGGGAGGGACTCCT	672511
rs215453337	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119412007	TGCTGCTTCCATTTT[A/G]CTGGGGTTTTCAGAA	672511
rs215470265	snp	C/G			missense, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119468075	AGCCTCCATCCAGAA[C/G]CAAAGGTGAGCAGCC	672511
rs215504961	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119451842	TCCCACTGCCTCCCA[G/T]CCCAGCTCCAACCAC	672511
rs215589403	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119453333	GTACATAGGGGCAGT[C/T]AGAGAAGGGGACGGG	672511
rs215626278	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119444810	CCACAGCACCCCACC[A/C]CACCCCCACACACGC	672511
rs215641646	snp	C/T			synonymous-codon	Rnf213	Mm_Celera	11:119442798	CACGCATGCTGTCCT[C/T]AGGAACTTCAGTGGT	672511
rs215720912	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119467435	CATCAAATAATGGAG[C/T]GAGCAACTGAGTAGC	672511
rs215724552	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119394202	TGCATTTGCCAGGAG[A/G]CTGGGGTGGGGGCGA	672511
rs215733553	snp	A/T			intron-variant	Rnf213	Mm_Celera	11:119445266	TATGAAGTATCAACA[A/T]AAATAACTTTTATAG	672511
rs215744481	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119478238	CCTGTATGTGACTTA[C/T]TTCACTTATTAAAGT	672511
rs215796166	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475247	GTGCACCACCACGCC[C/T]GGCTAAGGATGGCAT	672511
rs215837557	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119431908	CCCGCTTGCTGTGAA[G/T]AGCTGAAGGCCTTTT	672511
rs215895124	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119414329	ATCCTTCTGTCCCCT[C/T]AGACTGGCATCAGTA	672511
rs215922949	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119478860	TTTCAGTATATTACT[A/G]ATTGGTTTTTCCCTG	672511
rs215928969	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119413392	TGGCATTGCTGGTGC[C/G]CTTCTTTCCTCCCGT	672511
rs215950011	snp	C/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119472502	ACACCATCACACGTG[C/G]CTTGTTTTTGTTTTT	672511
rs216001565	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119470039	GCATCATAGGCATCC[C/T]TGAGGCTGCATAGTC	672511
rs216004709	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119401124	GGCCCTACAAACCTG[C/T]GTTAGTGCTGCAGTG	672511
rs216053828	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119455026	GATTTCTCCCAACTG[G/T]TCCTCCCTCGGTTCC	672511
rs216060692	in-del	-/TGTG			intron-variant	Rnf213	Mm_Celera	11:119412432	TTTATCACGTTTATT[-/TGTG]TGTGTGTGTGTTTCT	672511
rs216061447	in-del	-/GG			intron-variant	Rnf213	Mm_Celera	11:119392483	CACCTTCGGGTGCCT[-/GG]GGGGGGGGGGGAGAG	672511
rs216135803	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119454162	TACTTTTTCAAAAGG[G/T]GGTGCTAGGAATCCA	672511
rs216168524	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119461387	CAGAAATCCGCCTAC[C/T]TCTGCCTCCCAAGTA	672511
rs216185951	snp	C/T			synonymous-codon	Rnf213	Mm_Celera	11:119440542	AGACTGTGAGGCGTC[C/T]ATCTTTTGCAAGTCA	672511
rs216273038	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119437504	AATGAAGCTGCTAAG[A/C]AGTGGCGGTGCACAG	672511
rs216306892	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119446839	GTGTGTGGTATGAGC[A/G]TAGTAAGTGCGTGTA	672511
rs216307803	in-del	-/TG			intron-variant	Rnf213	Mm_Celera	11:119394957	TTATTGCCAGGTAAC[-/TG]TGGGGCGGAGCCTAG	672511
rs216323607	snp	G/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119480686	TTCCCCTCACCTTGA[G/T]GCTACAGCTAAGACT	672511
rs216352491	snp	C/T			intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119469241	CTAATTATTATTAGA[C/T]CTTTTCTTTATTTAC	672511
rs216355915	in-del	-/C			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119482719	TCACAGTTATGTGTG[-/C]TGTGGCTAAACAGCC	672511
rs216358621	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119433687	CTACTATTGCCGACC[C/T]CAAGGGCTTTGGCAA	672511
rs216439994	snp	A/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119474491	GAAAAATCCTTTTTT[A/T]AAATAAAAAGAGGGG	672511
rs216460042	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119404574	TGTGCACATTCTCAG[G/T]GGGGAGGGATTAGTG	672511
rs216498899	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119481541	TCAAGCTCTTTGGAC[C/T]GTCTGCACCTCAGTC	672511
rs216500666	snp	C/T			synonymous-codon, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473487	CCGGCTACTCACTCA[C/T]TTGGCTATGCTTGTG	672511
rs216518079	snp	G/T			intron-variant	Rnf213	GRCm38.p3	11:119396627	TAGGCCGCCAGCAGG[G/T]CTACGTGAGGGCGGA	672511
rs216538589	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119391975	GTGCGTGAGAGGGAG[A/G]TGCCATGACCAGAGG	672511
rs216551558	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119426644	CGCCCTGGGCTTTCA[C/T]AGGTGCGTGACAGCA	672511
rs216579155	snp	C/T			utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119486893	CAAACAAAGCACTTT[C/T]CAGTTCTCATGTCTT	672511
rs216579260	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119428935	CCCGCCCTCTTCCCT[C/T]GCACGTCCCCGCCCT	672511
rs216624452	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119461861	CCTATAGACCCTTAC[C/T]TACTACTCACCACTG	672511
rs216625149	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119472000	GCTATCACTGGTCCT[A/G]AATGCAATGTGGCTG	672511
rs216629278	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119448284	GTCAAATACTCATGT[A/C]CATAAAAACTAATTA	672511
rs216650871	in-del	-/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119478807	ATTTGACACTGGCTG[-/T]TTTTTTCACTGGCCT	672511
rs216736682	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119463491	GAGTTCCCTTCTTCC[C/T]GTAAAGGTCAAAACC	672511
rs216740743	snp	A/G			upstream-variant-2KB	Rnf213	Mm_Celera	11:119388106	TTGAGAGAAGGAGAT[A/G]CCATGGTTGCTAGAG	672511
rs216772358	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119448576	AAGAGAGAACCAGCG[A/G]TCACAGATCACCTTC	672511
rs216773366	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119438497	AGACAGACAGTGTAA[C/T]ATGTGAGTTGTAAGG	672511
rs216840868	in-del	-/TGGTGTGACC			intron-variant	Rnf213	Mm_Celera	11:119464474	AGCCACACCCCTTAA[-/TGGTGTGACC]TGCCAGCTCTCATAA	672511
rs216869706	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119439321	AGGAGACAACCTTAA[A/C]TTACAACTGGTTCTT	672511
rs216886476	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475380	ATTCCTGTCCAGCTG[A/G]GCCAAAGAAAGTCCT	672511
rs216894337	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119407658	GCTGGCAGGCTCACT[G/T]GGGCCTCACCACAGG	672511
rs216924402	in-del	-/GAGCAGTG			intron-variant	Rnf213	Mm_Celera	11:119407264	GCAAAGTAGGGTGAA[-/GAGCAGTG]GAGACTCAGGACTTG	672511
rs216993711	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119408402	GCCTCGCCTCCTGAC[A/G]TCTCCTCAGCTCTGC	672511
rs216999104	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119468192	GTAGAAACCTTACTA[A/G]AGGAAAGCTCTGTCT	672511
rs217023446	in-del	-/AT			intron-variant	Rnf213	Mm_Celera	11:119398175	TTCTTTGAACTGCAC[-/AT]GTTTTACTTTGGAAA	672511
rs217035311	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119433787	TCAGGAAGTCATACA[A/G]AATGGCATGTTGGGT	672511
rs217047124	snp	G/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475846	AAGAGCAGTTGGCGG[G/T]CACTCATAACCACTG	672511
rs217058166	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119396361	AGAGCTAGCTGGGCA[A/G]TGCTTGCTGCTCTCC	672511
rs217068898	snp	A/G			synonymous-codon, utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119469003	CATCCTCCTCTGTGG[A/G]CACAACCAAATTTTG	672511
rs217133355	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119395635	CCGAGACTCACCCTA[C/T]CCTGCTCCTGCCTAC	672511
rs217171653	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119427235	AACTCTCTTTTTGTA[C/G]AACAGGCTAGCCTTG	672511
rs217297714	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119428328	GTGTGTGTGTGTGTG[C/T]GTATGTGCACTTAGG	672511
rs217300936	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119432599	TTTTATTTATTTTTT[A/C]TGTGTATGGGCATTT	672511
rs217322517	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119432035	ATATGCGTGCCACAT[C/T]TACGTCTGGTGCCAG	672511
rs217338638	snp	A/T			intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119477513	CCGTCAGTAGTCATC[A/T]GAAGAGAATTGAGGG	672511
rs217356895	snp	A/C			upstream-variant-2KB, utr-variant-5-prime	Mir1932, Rnf213	Mm_Celera	11:119389454	ACCCAAACCAACCAA[A/C]CAACCAAACAAAAAG	672511
rs217426305	snp	C/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119471000	AGTGACACTACTGAA[C/G]GGGAAAGACATCCCA	672511
rs217466904	snp	C/T			intron-variant, nc-transcript-variant	Rnf213, LOC102639982	Mm_Celera	11:119478095	AACTGTTCCAATCAC[C/T]GTCTTTCTGTCCACA	672511
rs217467739	snp	C/T			synonymous-codon, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119470173	AGACCTGCTAGTTCA[C/T]GCCAGGACTTGGAGG	672511
rs217570061	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119398084	GGCAGACAACTGTCA[A/C]AAAGCAGTTTTCTAA	672511
rs217649976	in-del	-/GTGCCT			cds-indel	Rnf213	Mm_Celera	11:119436308	TCGTACAAGCTACCA[-/GTGCCT]GTGAAAGCAAGGCTG	672511
rs217653668	snp	A/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119465712	AAAAAAGAATTCTTT[A/T]AAAAAGGGAGGGGGA	672511
rs217719479	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119428726	TAGGTCGGTCAGGGA[A/G]CTCTAGGCTTTCTTT	672511
rs217727434	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119399918	AATCAGAAGGAAGGC[C/T]TAGACTGTTCCATCA	672511
rs217737321	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119445297	TTGGGAGCACCACAA[C/T]ATGAGGAGCTGTATT	672511
rs217763961	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119398737	TTTATTTTGAGACGG[C/G]ATCTCATTGGATAGC	672511
rs217796502	snp	C/T			upstream-variant-2KB	Rnf213	Mm_Celera	11:119387882	CTCTGGTAGGTACAG[C/T]ATGAAGGCTGCCAGA	672511
rs217831035	snp	A/G			upstream-variant-2KB	Rnf213	Mm_Celera	11:119387554	GAAGAGATAAGGAAG[A/G]GGGGACTATAATTCA	672511
rs217832575	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119401324	TTCGAGGCCAGCCTG[G/T]TCTACAGAGTGAGTT	672511
rs217838270	in-del	-/CC			intron-variant	Rnf213	Mm_Celera	11:119448491	ATAAATGTCGGGTTA[-/CC]GCCTGTAGAGCTGAG	672511
rs217864153	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119400521	TGAAATAAGTTTGGA[C/T]ACAGGACCTGATAAA	672511
rs217904302	snp	A/C			downstream-variant-500B, intron-variant	Mir1932, Rnf213	Mm_Celera	11:119390675	CAGAACTTTTGCGAG[A/C]CAGATGTCTGCCCTC	672511
rs217918529	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119466647	GTGTGTCACATGTGT[A/G]TGTGTTGTAAGGTTA	672511
rs217921201	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119457256	ACATTGTTTGAGATG[A/G]GGGCTGAGCTATACA	672511
rs217928979	snp	C/G			upstream-variant-2KB	Rnf213	Mm_Celera	11:119388150	GGTGAAGAGCAGAGT[C/G]CTGACGCCCAGAGCG	672511
rs217980453	snp	A/C			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119470632	TAATCCATCTAATTT[A/C]TCTTTGCTTTCTAAA	672511
rs218002430	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119462566	TTTTAGTGGGGAGGG[A/C]TGGAGTGGTGCTGGA	672511
rs218062933	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119471221	ATGGAATGAGGCAAA[A/G]CAGGATTCTTTCCCA	672511
rs218070620	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119427421	GCCTGAGCGCCGCCG[G/T]AGCACGAGGAGTCAT	672511
rs218072257	snp	A/G			missense	Rnf213	Mm_Celera	11:119436434	TGCAATCCCTCGTGT[A/G]CATGAGTGCCTTCCT	672511
rs218132236	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119456770	GATGGAAACAGTCTT[A/C]GATGCCTGGATATGG	672511
rs218173112	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119463980	TAGATATCCTGACAG[C/T]AAAGATCAAATTTGT	672511
rs218219269	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119428406	CTCTTTCACTATATT[C/T]AGTGAGACAGGGTCC	672511
rs218220471	in-del	-/T			utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119487237	TTGAACTAGGCATTA[-/T]TTTTTTTTTCTGTCA	672511
rs218354561	snp	C/T			intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119483247	CCATGCCATACTAGG[C/T]TTCTGAGTAAGACCA	672511
rs218382638	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119420779	ACTCACTCTGTAGAC[C/T]AGGCTGGCCTCGAAC	672511
rs218398140	snp	A/G			intron-variant, nc-transcript-variant	Rnf213, LOC102639982	Mm_Celera	11:119465170	CATGTAGTTCATACA[A/G]CGAAAGCATTTCTGA	672511
rs218425982	in-del	-/T			intron-variant	Rnf213	Mm_Celera	11:119461819	TTCGTCAGCAGCCAC[-/T]GAGACAATGGGTGCT	672511
rs218436883	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119456828	TAGGACAGTGTAAAC[A/G]GTTCTCAGTGCCACC	672511
rs218442827	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119430759	AACTTTGTAAGTTGT[C/T]TGCTGGCTCTGCTGA	672511
rs218457408	snp	A/C/G			intron-variant	Rnf213	GRCm38.p3	11:119418704	GAACATGGATCTATC[A/C/G]GGCTGGGTGATGGTC	672511
rs218556046	snp	C/T			downstream-variant-500B, intron-variant	Mir1932, Rnf213	Mm_Celera	11:119390781	AGCCTCCCCTGTCCC[C/T]GAAGCTGCAGCGAGA	672511
rs218587772	snp	C/G			upstream-variant-2KB, utr-variant-5-prime	Mir1932, Rnf213	Mm_Celera	11:119389999	TCGCTCTGGACAAGC[C/G]AGCTAGGCCGGCGCC	672511
rs218669253	snp	A/C			missense	Rnf213	Mm_Celera	11:119458814	CCCAAGGCTTGGTTA[A/C]AGCTTGTGAAGAATC	672511
rs218734416	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119437867	GCTCCCCGATTCTGA[C/G]TGCCTCCCTACGCAT	672511
rs218806035	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119429448	GTGAGACACCATGTG[A/G]TTGCTGGGATTTGAA	672511
rs218811782	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119450565	CTTAAGTGAACCTGG[A/G]TCATGGCTATGTGGT	672511
rs218826882	in-del	-/A			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119471385	CGCCATCATATATTT[-/A]AAAAAAAAATTAGGC	672511
rs218874729	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119460274	TCAGTAAGCATTCAG[G/T]TGCAGGAACAGGTAT	672511
rs218878816	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119438756	GACTCATATCAGGGC[C/T]ATTTGAGTGATGTTT	672511
rs218892777	in-del	-/AG			intron-variant	Rnf213	Mm_Celera	11:119455699	CTCTCAGCACTCGTC[-/AG]AGGCTGGTGCAGCCA	672511
rs218913042	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119394781	AGGGACCAGCCACAC[A/G]ATGGTATAGTATAGA	672511
rs218990071	in-del	-/CCA			intron-variant	Rnf213	Mm_Celera	11:119411266	GATTAGAGGTGTGAG[-/CCA]CCACCACTGCCCGGT	672511
rs219061227	in-del	-/TATTATTAT			intron-variant	Rnf213	Mm_Celera	11:119392641	AGCCTTTCTTTTTTC[-/TATTATTAT]TATTATTATTATTAT	672511
rs219102049	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119457944	CTGAGGACCACCAGC[C/T]CAGGGGTGGTGACAT	672511
rs219124512	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119485861	GGGCTCCCAGACCAG[C/T]ACAGGAGCTCAGCCC	672511
rs219129068	snp	A/G/T			intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119467557	AGTTAGCCAGTGTCT[A/G/T]TAACGGAGCCCCTGA	672511
rs219139768	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119432084	CAGATCCCCTGAAAC[C/T]GAGGTTACCATTGGT	672511
rs219151201	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119426547	CTGTCCTGCTGTTCA[C/T]ATCCGCAATGTGTGG	672511
rs219199863	snp	C/T			synonymous-codon	Rnf213	Mm_Celera	11:119458855	ACTGGAGCTCGTCTG[C/T]TCCGAAGGGTACTTG	672511
rs219221528	snp	C/T			synonymous-codon	Rnf213	Mm_Celera	11:119431707	CTGCTTGGAGGAGCT[C/T]GCCCGGCAGACGGAG	672511
rs219285314	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119461416	TACTGGGATTAAAGG[C/T]GTGCCCCACCACTGC	672511
rs219287362	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119413172	TCGGTCTGGCTCCAA[C/T]GTGTACATGTATGTG	672511
rs219313184	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119425535	GAACTACTTTGAGTA[C/T]ATGTCAAATATTATT	672511
rs219320383	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119485371	TATAAGTCTGTCAAC[A/G]CTTTAGTGTCTGCTC	672511
rs219342179	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119483625	GCATTTGGATTCCGT[A/G]ATGCACATGGATGAC	672511
rs219406593	in-del	-/AAC			intron-variant	Rnf213	Mm_Celera	11:119435681	AAAAAAAACAAAAAA[-/AAC]AAAAAGAGAAAAAGA	672511
rs219406964	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119461526	GTTGTTGTTGTTGAG[A/G]TAAGGTCTCACTATG	672511
rs219461572	snp	A/T			intron-variant	Rnf213	Mm_Celera	11:119460745	GAAGCCAGGTTCAGA[A/T]GAACACAGTGCAGTG	672511
rs219491377	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119453496	GAAACCCCTTGCTAC[C/T]CACATGATCTACAAT	672511
rs219519918	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119453860	GTGTGGTTTATGTAG[C/T]TTTTCACAGAGGTGG	672511
rs219521619	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119451950	CCTGACTGACCTGAC[C/T]GGGAGAAAGCCGACT	672511
rs219541894	in-del	-/TGGCACTTACC			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476380	TATTGAACTCTCTAT[-/TGGCACTTACC]TGGTACTTACCCTAT	672511
rs219564521	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119462097	TCACTTTCTTGGGTT[C/T]TAGGTTTGGTATTCA	672511
rs219580532	in-del	-/GC			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119466163	GGCTTAAGGCCTCTA[-/GC]TGGTGTCTTCATAGC	672511
rs219582073	in-del	-/TTCTTAACCACTGAGCCA			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475041	ACTACTCTTCCAGTG[-/TTCTTAACCACTGAGCCA]TCCTCCAGTGAAGAT	672511
rs219678164	in-del	-/GCTCGTCTCTGCCTG			intron-variant	Rnf213	Mm_Celera	11:119462754	CTCAGTAACCCTGCA[-/GCTCGTCTCTGCCTG]GCTTAGCCGCCAGTG	672511
rs219694157	snp	A/T			utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119486532	AGGGTAGTCAATTTT[A/T]TAAATTTTTTTACTT	672511
rs219718155	snp	C/T			utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119486681	AGGTGCTGATAAAAG[C/T]TGTAAAGCCTCATGA	672511
rs219777636	in-del	-/GCACAGAAG			intron-variant	Rnf213	Mm_Celera	11:119431080	AAAAAGGTCATAAGA[-/GCACAGAAG]GAAGGAAGGTCATCT	672511
rs219793185	snp	C/T			downstream-variant-500B, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119487581	GCACAAGTACACGTG[C/T]GCACACAGTTTCTTT	672511
rs219815478	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119413481	GAGCTCCATGCCCAG[C/T]CCAGCCCAGGGTTCC	672511
rs219828686	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119453398	AAAATTGGCGTGCCT[C/T]ACTTGTCTCCTGCTT	672511
rs219846106	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119426687	CGCAGTGTCATACAC[A/G]ATAAACTCATTGTCC	672511
rs219857462	snp	G/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119478381	GACCTGATGCCCTCT[G/T]CTGGCATGCAGACAA	672511
rs219859320	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119426672	GCATGTCTGGTGCAT[C/G]GCAGTGTCATACACG	672511
rs219907278	snp	C/T			intron-variant, nc-transcript-variant	Rnf213, LOC102639982	Mm_Celera	11:119477850	TCAGGGTGGTTTTGG[C/T]TGAGGTAGCTTGGGT	672511
rs219960335	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119425967	AAGACATTACTATGT[A/C]TCGTTTGACACATTT	672511
rs219989240	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119427301	TAAATGTATTTAAAA[C/T]CTTGTCATCTAAGTT	672511
rs220044142	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119454287	CTGTACTGAAATGCT[A/G]TCTAGTATATCATCC	672511
rs220094461	snp	G/T			missense	Rnf213	GRCm38.p3	11:119414427	ACAAGAAAGGAACTG[G/T]TGAAAGGGAAGAAGC	672511
rs220124790	snp	C/T			intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119464950	CTGGGTTAGCCCTAG[C/T]CCTGGGAGACATAGC	672511
rs220126845	in-del	-/CCAG			intron-variant	Rnf213	Mm_Celera	11:119445940	TCTCATAAAAGCTTC[-/CCAG]CCAGCATGGTCCTTA	672511
rs220141418	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119428820	CCCGCCCTCTTCCCT[C/T]GCGCGTCCCCGCCCT	672511
rs220141741	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119412518	GGACAATTTATTAGG[A/G]GTGACAGCAGGGACC	672511
rs220145345	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119415774	AGATGTCTGCCCTAA[A/G]CTTGCTGAGTGCTGG	672511
rs220154298	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119454308	TATATCATCCACATA[A/G]GCAAGTGCTCCAGTA	672511
rs220188765	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119464068	GCTGGGAGCTCATCT[A/G]TGGTCTGGAGAAGCT	672511
rs220220255	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119428517	CAGGGTGGAACAGCC[A/G]GGCTGTCATGCCTAC	672511
rs220226732	in-del	-/T			intron-variant	Rnf213	Mm_Celera	11:119463841	AGATAGTTTCTGCAG[-/T]TTGTCTGACATGGAA	672511
rs220240997	in-del	-/AAAAA			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119465747	AGTTTTCTATGATTC[-/AAAAA]AAAAAAAAAAATACA	672511
rs220262403	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119455203	CTGCGAGCCCCTCAT[A/C]CCCTTTACTCTGCCT	672511
rs220327158	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119445563	CCTCCTCATGTTTCT[C/T]TGTTCTGTCTTGAGA	672511
rs220341823	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119456528	GGGAAAGGAACAGAC[A/C]CTCAAGGCTACAGTA	672511
rs220387005	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119453689	AAGACCTCTGGAAGA[A/G]CAGTCACTGCTCTTA	672511
rs220447941	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119456920	GTTGAATCTGTTCTC[A/G]GGCTGGAGAGACAGC	672511
rs220472396	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119480452	TCTGATGACTGTAGC[A/G]TGTGTCAAGTTGACA	672511
rs220518268	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119448650	ACACTCACATGAGTA[C/T]AATTCAATTAACATA	672511
rs220520136	in-del	-/TC			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119466793	GAAGAGAACAGGAAG[-/TC]AGAAATCAGAGCAAT	672511
rs220546724	in-del	-/AGG			intron-variant	Rnf213	Mm_Celera	11:119444002	AGGCAGCATTCTAGC[-/AGG]AGGACCAGGGACATA	672511
rs220549206	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119403563	TGGTGGCTGGAGAGG[A/G]CTCCATAGTTAAGTG	672511
rs220554996	in-del	-/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119471381	AATCGCCATCATATA[-/T]TTTAAAAAAAAAATT	672511
rs220557660	snp	A/C			missense, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119480890	TAGCCTACACAATAA[A/C]ATGGTCTACACGGTG	672511
rs220596350	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119448425	GAGTGAGTTCCAGGA[C/T]AGCCAGGGCTACACA	672511
rs220596930	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119415642	ACAGCTGTGAGCCCC[A/G]GATTCTCTGCAAGAG	672511
rs220605607	snp	A/G			downstream-variant-500B, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119487830	AGGCCCCTTAGGAAT[A/G]GGAAACAAAGGCAGG	672511
rs220751256	in-del	-/GT			intron-variant	Rnf213	Mm_Celera	11:119454890	GGGCAGGAAGTGTTC[-/GT]GTGTGTGTGTGTGTG	672511
rs220754495	snp	C/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119482908	GCCCAACCCTAACCC[C/G]AGCCTTCCATTTTAT	672511
rs220755104	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119447684	CTTGTCTACCTTAGG[C/T]GAGCACTGCATCTGA	672511
rs220776898	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475980	CAGTCTGCATTCATT[A/G]CAGGAATTTGCTATT	672511
rs220802724	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119414945	GCAAGTGCTCCTGGG[C/T]GTGCTCCCTGCTCTG	672511
rs220803639	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119456374	AGACACAGAGCTGCA[G/T]GGAACACTCAGGGCC	672511
rs220956791	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119419502	GAAGTCAAACGTGAT[C/T]GTATGACTTCCTGTT	672511
rs220963685	snp	A/T			synonymous-codon, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119480830	CATCCTTCCAAGGCG[A/T]CAGGGCCTAGGCCTC	672511
rs221006041	in-del	-/G			intron-variant	Rnf213	Mm_Celera	11:119450852	AGAGCCTGTGTGGGA[-/G]GGCTGAAGTACCACA	672511
rs221045559	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119455438	CAAAATGGGTCATGC[A/G]TCATCACATCCTGAT	672511
rs221068969	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119404826	TCCATGGGATCTGTC[A/G]CCCTCTTGTGGCCCC	672511
rs221089841	in-del	-/A			intron-variant	Rnf213	Mm_Celera	11:119426414	GGTGAGGTGTGAGGC[-/A]AAAAAGTGTGACTGC	672511
rs221098905	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119408135	GCTCCCACGTGGTTA[G/T]GAGGAGGGTCTCTTT	672511
rs221148265	in-del	-/A			intron-variant	Rnf213	Mm_Celera	11:119429881	GAGAATAATTAGTTG[-/A]AAGCCAGCCTGCCTA	672511
rs221183224	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119474806	CAAAAGCCAGCACTG[C/T]TCATTGAGCTGACAG	672511
rs221187278	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119408677	GGAGTGCCGGGGTCA[C/T]GGAGACTCTAAGGAG	672511
rs221199296	in-del	-/CC			intron-variant	Rnf213	Mm_Celera	11:119391227	TTTCTTTCTCCTCCT[-/CC]CCGCCCCCCCATTTT	672511
rs221202991	snp	A/C			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119481786	GGATGCCCTCGAGTC[A/C]CTCGGCACAGAGGCC	672511
rs221205594	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119418392	GTTAGAGCAAAAGCC[C/T]GAGTCTCATCCTCAG	672511
rs221244997	snp	G/T			splice-acceptor-variant	Rnf213	Mm_Celera	11:119449723	TTGTTTTCTTCCTCA[G/T]TGTTCACAGTTCCTA	672511
rs221331728	snp	A/T			synonymous-codon	Rnf213	Mm_Celera	11:119443509	CATTGGCTACCATTC[A/T]GATGCCTGTGCCTCT	672511
rs221357652	in-del	-/C			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119465263	AAGAAAACAAACAAA[-/C]AAAAAAAAAAAAACA	672511
rs221360646	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119412409	ATTTTAAATAACTTT[A/G]AAAATATTTTATCAC	672511
rs221381061	snp	C/G/T			intron-variant	Rnf213	Mm_Celera	11:119395746	CGGGGGGGGGGGGGG[C/G/T]TTGATCCGAGAAAAA	672511
rs221386033	in-del	-/AC			intron-variant	Rnf213	Mm_Celera	11:119456931	TCTCGGGCTGGAGAG[-/AC]AGCTCTGGGGGTTGA	672511
rs221399718	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119452218	TTCTGTTATATTTTA[C/T]GTTTGAGTGTTTTGC	672511
rs221412243	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119400289	GGAATTATAAATGAA[A/G]ATTTCAAAGGAGAAA	672511
rs221474303	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119453579	ATTTATTATATGTAA[A/G]TACACTGTAGCTATC	672511
rs221479129	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119484592	TTGTACAAGTGTAGG[A/G]GCTTGTGTTTAGATA	672511
rs221527633	snp	A/T			intron-variant	Rnf213	GRCm38.p3	11:119445913	TCTGCCCCTGTACCC[A/T]CTACTCTATCCCTCT	672511
rs221562020	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119448731	GCTAAGTTATAGAAG[A/G]TTCCAGTGACTGTTC	672511
rs221587151	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119445424	AAAGCAGGGAGGAGA[C/T]TAAGTCATCTGTCAG	672511
rs221613668	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476918	TATTCAGGGTGCAGG[A/G]GGGCAAACCCTACAA	672511
rs221613698	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119485469	ATGAAGAGCAGTGGT[A/G]CTTGTACCTCCCAAG	672511
rs221652157	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119482615	GTCCAGTGCTTTCCA[C/T]AAAGGAAAGCAGGAC	672511
rs221722394	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473049	GCAAGCCTCTTCTCT[A/G]ATGCCTTCTTGGGGG	672511
rs221761096	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119472337	AGACCAGGCTGGCCT[C/T]GAACTCAGAAATCCA	672511
rs221761713	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119480040	GTCACACCCAGCACC[A/G]TGCAAGCTCTCTAGG	672511
rs221792625	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119407993	CATTTAACTGGGGCT[A/G]GCTTACAGGTTCAGA	672511
rs221810566	in-del	-/C			intron-variant	Rnf213	Mm_Celera	11:119402776	GTTTCCTGATGTGAT[-/C]CGCACTGGAGCCTGG	672511
rs221875723	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475467	TGGAAGTTGAGGACA[A/G]CTTTTGGGAGTTGGT	672511
rs221877551	snp	A/G			synonymous-codon	Rnf213	Mm_Celera	11:119443257	CACCCACCGAGTCAA[A/G]TGCCGAGTGCACACT	672511
rs222068185	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119412336	CCCCAGCCTGTGGCT[G/T]TACTCAGTGTAGCCT	672511
rs222073373	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119449590	ATGGCTGGTGGGGTT[C/T]ACTGTAACTTTGCCA	672511
rs222093155	in-del	-/CGGGTTG			intron-variant	Rnf213	Mm_Celera	11:119424875	CACGAGCCGCACTGC[-/CGGGTTG]CGGGTTGCGTTCCTT	672511
rs222093352	snp	A/T			intron-variant	Rnf213	Mm_Celera	11:119405602	AATAACCCTGCCCTG[A/T]GTGAAGGCTGTCATA	672511
rs222094669	in-del	-/TG			intron-variant	Rnf213	Mm_Celera	11:119394555	GAAAGAGAAACTGGA[-/TG]TGTGTGTGTGTGTGG	672511
rs222131464	snp	G/T			intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119477687	GAGTAGGTTGGGAAG[G/T]TCTGAGGTGCAGCAA	672511
rs222138584	in-del	-/T			intron-variant	Rnf213	Mm_Celera	11:119429331	CAGCCAGCTTCTGAC[-/T]TTTTTTTTTTAATAA	672511
rs222163081	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119393329	ATTTGTGTGAAGCGC[C/G]AACTGTTCAGATTCC	672511
rs222209870	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119398242	GCTCTTGCCCTTGTC[C/T]TTGCTCAGCAGAGGG	672511
rs222220930	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119414745	GGACCTTATGCCCTC[C/T]TCCTCAGGGGTTTCC	672511
rs222224372	snp	A/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119470291	CACATTTGCCTTTGG[A/T]GGCTTACAGGACCCA	672511
rs222247337	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119448460	ACCCTGTCTCGAAAA[A/G]CAATAAAAATAAACA	672511
rs222256699	snp	A/G			synonymous-codon	Rnf213	Mm_Celera	11:119441613	GCTGAATGACTCTGC[A/G]GAAAAGCTCTACATC	672511
rs222307485	snp	A/G			missense	Rnf213	Mm_Celera	11:119402668	GAGGAGTCCGATTCC[A/G]ATGCCTCCTGGACCA	672511
rs222347480	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119401765	CTGCCTCTGCCTCCC[A/G]AGTGCTGGGATTAAA	672511
rs222348914	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119415443	AGACCAGGCTGGCCT[C/T]GAACTCAGAAATCCG	672511
rs222362192	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119448687	CAGGTTGAGATTATG[C/T]CTTGTTTATAAATGA	672511
rs222425112	snp	A/G			missense	Rnf213	Mm_Celera	11:119441156	TTCTTAGTGACCTCA[A/G]GCGTGGTAGTGTGGA	672511
rs222444026	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119445346	GAAGGTTGGGAACCA[C/T]TGGTTTATAAGAAGA	672511
rs222446372	in-del	-/AC			intron-variant	Rnf213	Mm_Celera	11:119423433	TGGAGGGACGGACGG[-/AC]ACACACACACACACA	672511
rs222458229	in-del	-/G			intron-variant	Rnf213	Mm_Celera	11:119431517	CCAGGCTCTTGCTAT[-/G]GGTTGGCTGCTCCTG	672511
rs222499999	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119439599	GCTGGGCGTGGTGGC[A/G]CACGCCTTTAATCCC	672511
rs222522903	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119446606	TTCAAAACTCATACA[A/C]ACGTTCATGCGCATA	672511
rs222539216	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119396966	TGGGACAGTGTCTCC[A/G]TACAGAGGACCTGAG	672511
rs222573498	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119431369	AGACAGGTCTGGTAG[C/T]ACTATGGTGAGAAAC	672511
rs222574039	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119410450	GCTGGGGCTGGGTGG[C/T]GCCTCCTTTCTAGCT	672511
rs222585428	snp	A/G			intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119469461	GCTCTGGGGGTACTA[A/G]TTAGTTCATATTGTT	672511
rs222667464	snp	A/G			intron-variant	Rnf213	GRCm38.p3	11:119433919	CAGAAATTGTAAACG[A/G]CCATTAAGAAACTAC	672511
rs222692976	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119437083	AAGAGGTCCCCTCTC[C/T]CAGATACTGCCCACT	672511
rs222699807	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476093	TTCTAGAAGGCTGCC[A/G]CTATCTTAGCATCTA	672511
rs222725408	snp	A/C			intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119469422	CTAGGCCATCTTCTG[A/C]TACATATGCAGATAG	672511
rs222740664	snp	A/T			synonymous-codon, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119481218	ACGGGATCTGAATCC[A/T]CTGATCCTCTCCAAC	672511
rs222741084	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119479135	TTGGATTCCTGTCCA[A/G]AAATGACTCTTCACT	672511
rs222788900	snp	G/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119468430	CCTGGGATTACAGGT[G/T]TGCATTACCACACCA	672511
rs222790863	snp	A/C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476754	GAACTACTACCCTAC[A/C/T]GAGAGACCCACTAGG	672511
rs222813817	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119433000	TACACCCTGGGACCT[A/G]TGGGTGGAAGGCGTG	672511
rs222836345	in-del	-/CCCAGCAGGCGGCTGCAC			cds-indel	Rnf213	Mm_Celera	11:119410225	CAGCAGCTGTGAAAA[-/CCCAGCAGGCGGCTGCAC]CCCAGCAGGCGGCTG	672511
rs222861417	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119401595	GGAAAATTTGCCTTT[A/G]TACTATCTATTTACA	672511
rs222887603	snp	A/C			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119481766	TTTCCTGGGTTCTCT[A/C]TGTTGGATGCCCTCG	672511
rs222925003	in-del	-/AAA			intron-variant	Rnf213	Mm_Celera	11:119397133	TTAAAAACTAAATCT[-/AAA]AAAAAAAAAAAAAAG	672511
rs222963959	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119407509	GGTCCCGGGGACTGA[A/C]TGAACCCAGGGCCTC	672511
rs222977538	snp	A/C			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119471287	GGTATGCTGTGGGCC[A/C]TGTGTCACACAGTTC	672511
rs222980399	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119474750	AGTTGACCATGGACC[A/G]TGTCCATGCACACAG	672511
rs222996607	snp	C/G			upstream-variant-2KB	Rnf213	Mm_Celera	11:119388442	ACACCACCACACACA[C/G]AGATGGTAACAGGGT	672511
rs223036903	snp	C/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119478523	TGGTTGAGTGTCTTC[C/G]TTTGTGATATACACC	672511
rs223096581	in-del	-/G			intron-variant	Rnf213	GRCm38.p3	11:119394570	TGTGTGTGTGTGTGT[-/G]GGGGGGTCTCCGTTC	672511
rs223108336	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119467520	AGCAAACTAGTGGCT[A/G]GAACGGGTGCAATGA	672511
rs223124363	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119463113	TGCAAAACAAAACAA[A/C]AACAAAAAAAAAACA	672511
rs223168492	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119400539	AGGACCTGATAAAAC[C/T]GCCATTTCCTGAAAA	672511
rs223201812	snp	A/C			intron-variant	Rnf213	GRCm38.p3	11:119396383	CTGCTCTCCAGTCTT[A/C]CTGATTTTCCCATTC	672511
rs223323928	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119397214	TCAGAGGGAATGGGG[C/T]GATTTTTATAATGGA	672511
rs223395151	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473831	ACTGATACCAACTAG[C/T]TTTTTGCATTATGAG	672511
rs223460193	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119433318	AAAAGCAGGACGTGG[A/G]TCAAACCAAGACCTT	672511
rs223490609	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119445169	CAAGAGAGAACAATG[G/T]CTGACACCATGTCAA	672511
rs223504668	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119396741	CTCCCCTTTACTAGA[C/T]GTTCTATGGAAAACC	672511
rs223531763	snp	A/T			intron-variant	Rnf213	Mm_Celera	11:119395923	TTTGGAGAGTCAGTT[A/T]TGTTGGATGGTGTTT	672511
rs223549530	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119434017	CCACATGGTGGCTCA[C/G]AACCTTGCATTACTC	672511
rs223600770	snp	C/T			downstream-variant-500B, intron-variant	Mir1932, Rnf213	Mm_Celera	11:119390843	CCCATCTGCTTTTTT[C/T]TTAGTCTAGCCCGGG	672511
rs223656857	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119405478	CTTGCCATTGGCCAT[A/G]GACTCTCAAAGGTGC	672511
rs223671207	snp	A/G			missense, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119465953	TCAGAGAGGAAGGTC[A/G]CTTCCTTAGGACATA	672511
rs223695790	snp	A/G			missense	Rnf213	Mm_Celera	11:119437669	TAAAAGCAAAGCTAC[A/G]TGACGAGACGGTCCC	672511
rs223697094	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119444054	TGGGTGGAAAGAAGG[A/G]GATATCGGAATTTCT	672511
rs223723155	snp	G/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119472400	GGCATGTGCTAGCAC[G/T]ACCCGGCGTTTATTT	672511
rs223757528	snp	A/T			intron-variant	Rnf213	Mm_Celera	11:119432843	AGCTCTTGTCTACAC[A/T]GGGTGTTTTTTTATA	672511
rs223813289	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119406446	GGTGGAGCACCAGGC[C/T]GTGCAGTAGGAACTG	672511
rs223828954	in-del	-/AT			intron-variant	Rnf213	Mm_Celera	11:119423595	ACACACACACATTAC[-/AT]ATATATATATGAGTA	672511
rs223855479	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119438867	TGTCTTGGATAATCC[A/G]TGTTGGTCAGCTGGG	672511
rs223861339	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119444903	TGACTTCATGGAGGG[A/G]CAGCAGTCCACAGAG	672511
rs223861656	snp	A/T			intron-variant	Rnf213	Mm_Celera	11:119432391	AATTAAATTACTTTT[A/T]AAAAATATTTATTTA	672511
rs223903610	snp	C/T			intron-variant	Rnf213	GRCm38.p3	11:119393027	GGCAGTCACGTGACA[C/T]GAGGCTGAGCTTTAT	672511
rs223912248	snp	A/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119469812	AGCAAGAGGAAGATG[A/T]ACTCAATAGTAATGT	672511
rs223921076	snp	A/G			missense, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119477103	AGCCAAGATGAGCGC[A/G]TCAGCTCCAACCCTG	672511
rs223923433	snp	C/T			synonymous-codon, downstream-variant-500B, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119469048	CTTGGCCTTCTATCC[C/T]GTCAACATGGCGGTA	672511
rs223939039	in-del	-/A			upstream-variant-2KB	Mir1932, Rnf213	Mm_Celera	11:119389084	TAAATAAGTGCAATT[-/A]AAAAAAAAACTTTAA	672511
rs223951838	in-del	-/CA			intron-variant	Rnf213	Mm_Celera	11:119412223	GTGTGTGTGTGAGTG[-/CA]TGTGTGTGCACACGT	672511
rs224052702	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119439460	GTTGGCAAGATGACC[C/T]TGGATAACAAGTATT	672511
rs224071670	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119429670	TGACAAAGCCAAGGC[A/G]GAGGAGAGGAAAGAT	672511
rs224116873	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119461673	GAGCTGCCATGTGGG[G/T]AATGGGTATCAAACC	672511
rs224124178	in-del	-/AG			intron-variant	Rnf213	Mm_Celera	11:119448562	TCCCTCCACGAGGGA[-/AG]AGAGAACCAGCGGTC	672511
rs224225234	in-del	-/GTGTGCT			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473631	GCCTGTGGGTTATAA[-/GTGTGCT]GCTCATGCCTCGTCT	672511
rs224234627	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119467655	TATATCTATGGCTTA[C/T]TCTGCTCCTGACTGA	672511
rs224307380	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475519	TCTCTCTTGTTATGG[C/T]TGCTACTCTGCATAT	672511
rs224351976	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119459148	AAGTTACAATGTAGG[C/G]AAAGTAGAAGGGACC	672511
rs224369153	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119395876	AGACAGAGTCCCCCA[C/T]GAGGGAGTGTAAAGT	672511
rs224406405	snp	G/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119468264	TTTTTCTTCAGTGCT[G/T]GGGATACTGGTGTGT	672511
rs224488033	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119400882	TTAAAAAAAAAAAAA[A/G]AAAGAAAGGTAAGAC	672511
rs224488899	snp	C/T			nc-transcript-variant, intron-variant	Mir1932, Rnf213	Mm_Celera	11:119390502	AGCCTGGCCCTGAGT[C/T]TCCGACCCCATTAAC	672511
rs224498867	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119460539	AGCATACTGGTGGCG[C/G]CGGCAGCAGCCACAG	672511
rs224562992	snp	A/T			upstream-variant-2KB	Mir1932, Rnf213	Mm_Celera	11:119389084	TAAATAAGTGCAATT[A/T]AAAAAAAAACTTTAA	672511
rs224565961	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119393502	CTAAGTAAGACGGGA[A/G]CCTTGTCCCAGCCCT	672511
rs224593692	snp	C/T			upstream-variant-2KB	Rnf213	Mm_Celera	11:119387905	CTGCCAGAGTGTCAC[C/T]ACAGGCAAAGGGCCC	672511
rs224601445	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119449707	CAGCACAGTAGAATT[C/G]TTGTTTTCTTCCTCA	672511
rs224618355	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119391211	GGTTTGAGAAGCAGA[A/G]CTTTCTTTCTCCTCC	672511
rs224684419	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119432262	TTATTCTGAAACTCG[C/G]TCTGTAGACCAGGCT	672511
rs224732295	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119437237	TTGTTGCAGTTTCTT[C/T]CCTCTGGGAGTGCTG	672511
rs224762082	snp	A/G			missense	Rnf213	GRCm38.p3	11:119436068	GCCAGCTGACAGAGA[A/G]GGGAGATGTCATACA	672511
rs224779619	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119429913	GTATTCAGACTTTGT[C/T]TTTCCCCTACACTAA	672511
rs224790573	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119424518	CTAGGTGTGGTGGCA[C/T]GTGCCTTTAATCCTA	672511
rs224811297	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119470389	TCTGAGAAAAGAGGG[A/G]ACTCTGAGCTACACT	672511
rs224842667	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119428693	TTTCCCACCATAGGC[A/G]GGGCACCTCATGAGC	672511
rs224883129	in-del	-/TAAG			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476942	CCTACAAGGAACTGT[-/TAAG]TATAACAGAAAGCAG	672511
rs224901103	snp	A/C			missense	Rnf213	Mm_Celera	11:119430461	CCCTTGTTATGACAA[A/C]TTCTACACACTCTAT	672511
rs224901524	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119425899	AAATGCCAGGATTAT[C/T]GATAAGTACCACCAT	672511
rs224907491	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119418609	TATCAATAGCTTTTT[C/T]AACTTCTATCTTAAT	672511
rs224955745	snp	G/T			intron-variant	Rnf213	GRCm38.p3	11:119432761	TCTGGAAGAGCAGCC[G/T]GTGCTTTAGCCACTG	672511
rs224990858	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119429013	GCTTATCTACCTTGC[C/T]GAGTAAGAGACAGAC	672511
rs224992141	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119461561	TCTGGCTATCCTGGA[A/G]CTCACTATTTAAGTC	672511
rs225045294	snp	A/G			synonymous-codon, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119466240	ACTGGCTGAAGACAA[A/G]CGGCGCTTCCTGAAG	672511
rs225057464	snp	A/C			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119465412	TGATGTCCAGGCTAT[A/C]GTTGCTCTGTAAGTG	672511
rs225090953	snp	C/T			synonymous-codon	Rnf213	Mm_Celera	11:119420085	TTTGGGGAGAACCTG[C/T]TACAGATCTACTTGA	672511
rs225108831	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119433961	AAGAATGGGTCAGCC[A/C]CTGTGGCTTTTGCAG	672511
rs225150576	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119468502	TTTTTTTTTTTTTTT[C/T]AGGGTATCATGTAGT	672511
rs225154319	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119456715	GAAATCATTAAGAAT[C/T]TAGCCTTGTTTGATT	672511
rs225164239	snp	A/G			synonymous-codon, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119467987	CTGCAGAAGCCCCAA[A/G]CCCCAGCAGACAGCC	672511
rs225200591	in-del	-/CGACTTTTAATGTTCCCT			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473223	TGACAACGACGACGA[-/CGACTTTTAATGTTCCCT]CGACTTTTAATGTTC	672511
rs225227722	snp	G/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119471207	ATACTTCCTTGTCCA[G/T]GGAATGAGGCAAAGC	672511
rs225241426	snp	A/C/G			utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119486752	ACTCACTGAGATCAC[A/C/G]GGACAGAGAGTGGAG	672511
rs225261696	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119457087	TTGGTTACCTGTATA[C/T]ATGCTTGTGCGCACA	672511
rs225279055	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119459848	TGTACACAGGGAAAG[C/T]GCCCTCCTATCCATT	672511
rs225328624	in-del	-/TTTTTTT			intron-variant	Rnf213	Mm_Celera	11:119415709	CCCAGTATCATTACC[-/TTTTTTT]TTTTTTTTTTTTTTG	672511
rs225363385	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119451236	TGGTCTTTGGGATTC[A/G]GAGTCAAGTTGGTAG	672511
rs225384457	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119464145	TTTCCACCATGGGCC[C/T]GTGAGTGTGGCCCAG	672511
rs225400236	snp	C/T			upstream-variant-2KB	Mir1932, Rnf213	Mm_Celera	11:119388568	TTCATGGCATGCCCT[C/T]CATGACTCCTTTCTC	672511
rs225475930	in-del	-/A			intron-variant	Rnf213	Mm_Celera	11:119464511	ACCCTTAAAGGGGTG[-/A]ATTGCCTCTATTCTA	672511
rs225515480	snp	A/G			downstream-variant-500B, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119487636	AGTGTTTCTGCTGTA[A/G]TATCCAGTAGGGTTC	672511
rs225587420	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119485669	TCTGCTTTATCATGT[C/T]TCGGGTTATAAAACA	672511
rs225599214	snp	C/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119484971	GCATGGTGGCACATA[C/G]CTATAATCACAGCAC	672511
rs225615411	snp	A/G			missense	Rnf213	Mm_Celera	11:119456236	GTGGCACAGCAGCAA[A/G]AACTCCTGCAGAGCT	672511
rs225885148	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119455363	TTTAAAGGGCCAGAT[A/G]CACAAAATAAATCAT	672511
rs225911023	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	Mir1932, Rnf213	Mm_Celera	11:119389971	GAAGGCCGTGGGCAC[A/G]CAGCGGCTGTAGTCG	672511
rs225920740	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119432443	ATAGCTGTCTTCAGA[A/C]ACACCAGAACAGCGA	672511
rs225947416	snp	A/G			missense	Rnf213	Mm_Celera	11:119418118	AGATGGCCCTGCTGC[A/G]CGTGGATGAGTACCT	672511
rs225957088	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119431870	ATGTTTTACTCAGAC[A/G]GTGTCTCGCTCCTTT	672511
rs225977258	snp	A/G			missense, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119465055	TGACACAGTTAGAGA[A/G]GAAGGCGTTCCTAAC	672511
rs225989011	in-del	-/ATGTATGT			intron-variant	Rnf213	Mm_Celera	11:119431986	TGTAACAGTGATTTC[-/ATGTATGT]ATGTATGTATGTATG	672511
rs226001543	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119429367	TTATTTATTATTATA[C/T]CTAAGTACACTTTAG	672511
rs226023277	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119427074	TGCGTCACATGCCCA[G/T]TTGTTTCATGGATTT	672511
rs226027715	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119425101	CAGTGTGTGAGGAGA[A/G]GGCTCCAAGAAATGT	672511
rs226105434	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119412869	TTTTTTATTTTGTGT[A/G]TGTGTACGTGTGTAC	672511
rs226133455	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119427474	ACCCAGGCTCTGATC[C/T]GTGTGCTCTCCTTCT	672511
rs226135289	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119414153	GCATGCACCAGCACC[A/G]CCCGGCAGGCTTTAA	672511
rs226151763	snp	A/T			intron-variant	Rnf213	Mm_Celera	11:119457846	ACTCAAGCCATGCAG[A/T]ATCCTGGAGGCAGGA	672511
rs226180193	in-del	-/TGCTGC			intron-variant	Rnf213	Mm_Celera	11:119396504	AGGTTATGCCACCAT[-/TGCTGC]TGCTGCTGCTGAAAC	672511
rs226181298	in-del	-/GTATGTAC			intron-variant	Rnf213	Mm_Celera	11:119432007	TATGTATGTATGTAT[-/GTATGTAC]GTATGTATGTATATA	672511
rs226184591	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119426272	GTGGAGGGACCCGCA[C/T]AGGCAGGGCTGCTCT	672511
rs226197581	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119461805	TGTGGCCATGACTGT[G/T]CGTCAGCAGCCACTG	672511
rs226207714	in-del	-/CG			intron-variant	Rnf213	Mm_Celera	11:119435243	GGTCTGCAGGATGTA[-/CG]GTACCCCGATTCACA	672511
rs226236192	in-del	-/AT			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119477023	TGTCTGAATTCCAGA[-/AT]ATTCTGTTTCATTCT	672511
rs226288311	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119428990	TTCCCTCGACTCTGG[A/C]AGACACAGCTTATCT	672511
rs226301013	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119414989	TGGCACAGTCACCCC[A/G]CCTCTGAGTGTGCCC	672511
rs226327602	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119453789	TGTGCATATAAGTGC[A/G]CATGCATGAGGAGGC	672511
rs226352053	in-del	-/AC			intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119464892	AGTCATGTGTGTCAG[-/AC]ATCCAGGTGCTGGGG	672511
rs226360134	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119454978	TAACTCCCTACCAGC[C/T]CTCCTTCCAGTTTCC	672511
rs226362642	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119453181	AACAGAACTCTAGTC[C/T]TCTGCAAGAGCAGTA	672511
rs226383558	in-del	-/A			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119478395	TGCTGGCATGCAGAC[-/A]AGTATGCACAGAGTA	672511
rs226387743	in-del	-/A			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119465696	GAAGAAAATATTAAT[-/A]AAAAAAGAATTCTTT	672511
rs226409513	in-del	-/C			intron-variant	Rnf213	Mm_Celera	11:119432805	CTCCTCCCCATTTAG[-/C]CTCCTCCTCCAGAAG	672511
rs226421801	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119446800	ATTGCAAGTTAAAGG[A/G]CAATAACTAGATAGA	672511
rs226429745	in-del	-/TTTGCCATGTTC			intron-variant	Rnf213	Mm_Celera	11:119431050	CAATTCATGGCCTCT[-/TTTGCCATGTTC]TTTAAAAAGGTCATA	672511
rs226450885	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119455558	GCAACCAGTCCTCCT[C/T]GTGGAACCACAAGGT	672511
rs226451504	in-del	-/ACACAC			intron-variant	Rnf213	Mm_Celera	11:119446620	CACGTTCATGCGCAT[-/ACACAC]ACACACGCGCGCGCA	672511
rs226458771	in-del	-/GAT			intron-variant	Rnf213	Mm_Celera	11:119398820	TCACCTGGCCATTTA[-/GAT]GATGATGATGATTTT	672511
rs226466219	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119466909	CAAATGGAACTAAAA[C/T]GCCTTATTTTCTTCC	672511
rs226475753	in-del	-/A			intron-variant	Rnf213	Mm_Celera	11:119448443	CAGGGCTACACAGAG[-/A]AACCCTGTCTCGAAA	672511
rs226479271	in-del	-/C			intron-variant	Rnf213	GRCm38.p3	11:119416913	AGGCAGAGGCAGGGG[-/C]CAGGGGCCAGGGGCC	672511
rs226500203	snp	C/G			utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119486857	TCTCTCCCCAGCACT[C/G]CAAGTGGGAATAGGG	672511
rs226519799	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119447892	AAATACCCGTGCCTC[A/G]TGCACCTTTACTAAT	672511
rs226627897	in-del	-/T			intron-variant	Rnf213	Mm_Celera	11:119432849	TGTCTACACTGGGTG[-/T]TTTTTTATAACACCC	672511
rs226634684	snp	A/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119478826	TTTCACTGGCCTTCT[A/G]CCTGGGGGTGAGATA	672511
rs226654565	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119456997	TTCCCAAAACTCACA[C/T]CAGGCAGCTGCTCAC	672511
rs226715483	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119422439	GGGATCAAAGGCGTG[C/T]GCCTCCACTGCCTGG	672511
rs226719270	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119481937	GGAGATCCTTCCAGT[C/T]CACTTAAGTACATTG	672511
rs226731717	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119481521	GCCTCCTGGCTGTGG[C/T]GATCTCAAGCTCTTT	672511
rs226831759	snp	A/C			missense	Rnf213	Mm_Celera	11:119430382	CAGAGTCACTGAATA[A/C]TCTGGATAAGGACCC	672511
rs226856644	in-del	-/TTGT			intron-variant	Rnf213	Mm_Celera	11:119463912	AAGGTGGGCTGTGGG[-/TTGT]TTGTTTGTTTGTTTG	672511
rs226882693	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119451018	CTGGAAGCTGGTGGT[A/G]CTGGCTCCTCTCTGT	672511
rs226971286	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119460588	ACACAAGCTCCACAT[C/T]CTTTCTCCCTACACT	672511
rs227006587	snp	C/T			synonymous-codon, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119482966	AATCAGTACCATCAG[C/T]GGACAGCTACAGTCC	672511
rs227023256	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119419788	AGTCCTCCGATAGTA[C/T]AGCAAGTGCTTTTGA	672511
rs227137139	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119420390	TTGGGTTGGAGGGAG[A/G]GAGGGAGGTGGTAGG	672511
rs227149838	in-del	-/G			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119467357	CTCTGATGGTAAGAC[-/G]GGTCTGGGCTTCTCT	672511
rs227249572	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119459360	AAGCACCTTCCAGTT[A/G]CCTTGTCTGCAGCCC	672511
rs227272809	snp	G/T			synonymous-codon	Rnf213	Mm_Celera	11:119410254	TGCACCCCAGCAGGC[G/T]GCTGCACCGGAGCCT	672511
rs227287153	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119408332	AATGTCCACAGGGGG[A/C]CCCAGGTGTGTCCCA	672511
rs227287529	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119422969	TGTCAGTTTGCTTTA[C/T]TTTTCTACCTTGTGG	672511
rs227315983	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119407167	TCTGGAGTTGAGGGC[A/G]TCTCCACAAATGGTC	672511
rs227346007	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119418504	TGGGGTGGGGGTGGT[A/G]GTGGCGTGTAGATTT	672511
rs227392100	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119409345	TGGTGCCTACTGAAG[C/T]CAGAGCCAGAGCATT	672511
rs227403974	in-del	-/C			intron-variant	Rnf213	Mm_Celera	11:119451176	TAATATGTTTAAAAT[-/C]CATAAACTCCATCTC	672511
rs227411280	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119457228	AGGAGATCAGCGCAC[A/G]TCTTCAATGCGAACA	672511
rs227442875	snp	C/G			intron-variant	Rnf213	Mm_Celera	11:119461070	AGGAAGGCTGACCCT[C/G]ACCAAGGTCAACATT	672511
rs227446575	snp	A/T			intron-variant	Rnf213	Mm_Celera	11:119450345	GATTCTTAGAGATGT[A/T]CTCCTGGTGGTATTA	672511
rs227474912	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119451845	CACTGCCTCCCATCC[C/T]AGCTCCAACCACATC	672511
rs227497328	snp	C/T			synonymous-codon	Rnf213	Mm_Celera	11:119448782	TGTGCATATTGATGA[C/T]CTCCGCAGATCAACA	672511
rs227535999	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119451383	GTCTTCTGAATGGCA[G/T]GCCTTGGAGCCCGTT	672511
rs227539661	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119458173	CCAGGGGATTTTCCA[A/G]TTTTCTTTTCTACAC	672511
rs227539809	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119448549	TAGTTCTCCAGGCTC[C/T]CTCCACGAGGGAAGA	672511
rs227553778	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119451292	CTCTGTAGCTTTGTC[A/C]GTGGCTGCCTCTCAC	672511
rs227570162	in-del	-/A			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473739	ATCCATTTCTTTTTT[-/A]ATTATTAATATTTTT	672511
rs227626764	snp	A/T			intron-variant	Rnf213	Mm_Celera	11:119445105	AGCACACCCTCAGGA[A/T]ATTGGAGTCTGTGGT	672511
rs227702502	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119483171	CCAGTATTGCCGGTA[C/T]TCAGGAGGAAGAGGC	672511
rs227704442	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119426558	TTCACATCCGCAATG[C/T]GTGGTGTGGCCTTTG	672511
rs227713418	snp	A/C			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119478140	GCAGTCACTGGAGAA[A/C]AGTGGAGAAGAACGG	672511
rs227765735	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119411132	TGGTGGAAAATAAGT[A/G]TTTCTTTTTAAAATT	672511
rs227812578	snp	A/C			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119478573	TCATCTGCTAATGGG[A/C]ATCTAAGTTGAAACT	672511
rs227816383	snp	G/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476222	CTGTTCTTAGTAGTT[G/T]GGTTCTGAATGGCTT	672511
rs227830383	snp	C/T			synonymous-codon, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119483730	AAGTCAGAACAGCGG[C/T]TGCGACTGAACAAAG	672511
rs227830489	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475828	TGAACTCACGACCTT[C/T]GGAAGAGCAGTTGGC	672511
rs227880449	in-del	-/GCGCGCGCGCGC			intron-variant	Rnf213	Mm_Celera	11:119428328	TGTGTGTGTGTGTGT[-/GCGCGCGCGCGC]GTATGTGCACTTAGG	672511
rs227890376	in-del	-/CTT			intron-variant	Rnf213	Mm_Celera	11:119456099	TTTTTGTGGCAGTAA[-/CTT]CTTCTGTAGATTTAA	672511
rs227930809	snp	C/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119471526	TCAATCAATTTGGGA[C/T]TCAAACTCAGTTTTA	672511
rs227943194	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119413241	CATCAGATCCCCCAG[A/C]ACTGGACATGCAGGC	672511
rs227953333	in-del	-/T			intron-variant	Rnf213	Mm_Celera	11:119393870	AATAAAGATATAAAA[-/T]TAAAAGAAAAGCGAG	672511
rs227959236	in-del	-/GAGGACCT			intron-variant	Rnf213	Mm_Celera	11:119396971	CAGTGTCTCCGTACA[-/GAGGACCT]GAGTTCATTCCGGCA	672511
rs227963431	in-del	-/TT			intron-variant	Rnf213	Mm_Celera	11:119453539	ATTTTTTTCTTTTTC[-/TT]TTTTTTTTTTAAAGA	672511
rs227977248	snp	A/C			intron-variant	Rnf213	Mm_Celera	11:119452945	AGATGCTGAGCTTGG[A/C]AGAATCTGTGCTTCG	672511
rs228169476	snp	G/T			intron-variant	Rnf213	Mm_Celera	11:119453862	GTGGTTTATGTAGTT[G/T]TTCACAGAGGTGGTG	672511
rs228188141	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119401868	GGCTAGAAATAATTC[A/G]TACGCAATTTCCTCA	672511
rs228259907	snp	C/G			utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119486803	GCTGGAACTAGAGTG[C/G]GCTGTGGAGTACTTG	672511
rs228262432	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119412963	TGGCCAAGGTTAGCA[A/G]AGAGCCAAGTCAGAC	672511
rs228328856	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119399777	TCATTTGCAAAGATG[C/T]TGTGACCAAGCCAAT	672511
rs228328914	snp	C/T			intron-variant	Rnf213	Mm_Celera	11:119414049	TTTCTCTGTGTAGCC[C/T]TGGCTGTCCTGGAAC	672511
rs228374170	snp	A/G			intron-variant	Rnf213	Mm_Celera	11:119414140	GCTGGGATTAAAGGC[A/G]TGCACCAGCACCGCC	672511
rs228403551	snp	C/T			synonymous-codon	Rnf213	Mm_Celera	11:119446167	CCAGGCAGACTTTGA[C/T]GATGGCACCCGTAGC	672511
rs228416957	snp	G/T			intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119478762	GCTCAACTAGCAATG[G/T]TATTCCTTTTTCTCC	672511

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