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

Cpne1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs262992947	in-del	-/ACTTTTGTT			intron-variant	Cpne1	Mm_Celera	2:156078853	TGCATCGTCTCATGA[-/ACTTTTGTT]ACTTTTATTACTGGG	266692
rs262999842	snp	C/T			intron-variant	Cpne1	Mm_Celera	2:156073787	CTACCCTGCCACCTC[C/T]TGTCCACTCACATTC	266692
rs263035437	snp	A/G			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156107319	ACAGAGCCAATCTAC[A/G]TACAAGAAACACCAT	266692
rs263052005	snp	A/G			intron-variant	Cpne1	Mm_Celera	2:156094351	ACTTAAGGATCTTTC[A/G]TTCTGCACTACTACT	266692
rs263086082	snp	A/G			intron-variant	Cpne1	Mm_Celera	2:156075458	ACAACACTGATGGGG[A/G]CCAACCTAGTCACTA	266692
rs263191926	snp	A/G			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156104789	TCTACCATGTGGGTC[A/G]TAGTTAAAACTCAGA	266692
rs263235369	snp	A/C			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156111514	CGCAGGCCGCGAGGC[A/C]ACCCGATGCTGGCCG	266692
rs263255385	snp	C/T			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156100129	TTTAATCCCAGCACC[C/T]AGGAGGCAGAGGCAA	266692
rs263264698	snp	C/T			intron-variant	Cpne1	Mm_Celera	2:156090472	GTCCTGTACCTGAGG[C/T]TGAAATGTTTCCTTC	266692
rs263451387	snp	A/C			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156110329	GCCTTGTGAAATCAC[A/C]TAAACACAAACATTT	266692
rs263468331	snp	A/G			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156099408	GCTCCAGGCCAGGGA[A/G]GGCTTCATAGTGAGA	266692
rs263570450	snp	C/G			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156101767	GAATGACGGACTGGC[C/G]CTAGAATCAGAGGTG	266692
rs263579495	in-del	-/A			downstream-variant-500B, intron-variant	Rbm12, Cpne1	Mm_Celera	2:156094407	CAGTTTTATACTCCG[-/A]AATACAATGCTCTTT	266692
rs263584197	snp	A/G			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156102607	ACAGAGTGAGTTCCA[A/G]GACAGCCAGGGCTAC	266692
rs263666764	snp	C/T			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156101564	ATAAATCAAATACAG[C/T]CACATTATATATTTA	266692
rs263679163	snp	A/C			intron-variant	Cpne1	Mm_Celera	2:156088028	GACCACTATTAATGA[A/C]TTCAGCCTCACCTGA	266692
rs263904669	snp	C/T			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156100355	TACTTGTAATTCTAT[C/T]ACTATTAGTTAAAGG	266692
rs263997856	snp	C/T			intron-variant	Cpne1	Mm_Celera	2:156090061	GTTCACCAAGACATT[C/T]ATCACCCTGGTTTCC	266692
rs264007112	in-del	-/GTATGATGATCAACAAA			intron-variant	Cpne1	Mm_Celera	2:156089582	GGGGAAAACATAAGT[-/GTATGATGATCAACAAA]GTTGAGTTCCAAAGA	266692
rs264063158	snp	A/G			utr-variant-3-prime	Cpne1	Mm_Celera	2:156072240	AATCACAGTAAATCG[A/G]ATCTCTGTTGGGAAG	266692
rs264208209	snp	A/T			intron-variant	Cpne1	Mm_Celera	2:156089291	GGCATTTTTATTTGC[A/T]TTGCCATCATTAAAT	266692
rs264241713	snp	C/T			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156099019	AAGAACTATCTGAGG[C/T]TGCAGAGGTGACTCA	266692
rs264262619	snp	A/G			intron-variant	Cpne1	Mm_Celera	2:156086445	GCAGGATCTCATAGA[A/G]CATGCAAAGCCCTCC	266692
rs264320824	snp	C/T			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156106742	CCAAGTAAGAACAAA[C/T]ACAAGGTATGGGCCT	266692
rs264450106	snp	G/T			intron-variant	Cpne1	Mm_Celera	2:156085674	TTGAGTCAACCAAGA[G/T]TTTACATAATGAAAA	266692
rs264736332	snp	A/T			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156110615	CAAAAATTACAGCTC[A/T]AACTATCCAAAAAGC	266692
rs264769222	snp	C/T			intron-variant	Cpne1	Mm_Celera	2:156082281	ATCTGCAGAGTCTTG[C/T]TAGCTGCCTACTCAG	266692
rs264905556	snp	C/T			intron-variant	Cpne1	Mm_Celera	2:156093190	CAAGCTCTGTTGTGA[C/T]TCAAGGGATGCGGAA	266692
rs264915016	snp	C/T			intron-variant	Cpne1	Mm_Celera	2:156083647	ATCAGGCCCTTTTCA[C/T]CTGAATGAATGCATA	266692
rs264978555	snp	A/C			intron-variant	Cpne1	Mm_Celera	2:156076624	ATGGTCTCTGTAGAC[A/C]AGGCTGGCCTTGAAC	266692
rs265104175	in-del	-/A			utr-variant-3-prime	Cpne1	Mm_Celera	2:156071888	ATAGATATATTTTTT[-/A]AAAGGGTAACATATA	266692
rs265111541	in-del	-/GT			intron-variant	Cpne1	Mm_Celera	2:156078245	CACCTGAGAGGGGGC[-/GT]GTGTGTGTGGATAAA	266692
rs265124681	snp	A/C			synonymous-codon, intron-variant	Rbm12, Cpne1	Mm_Celera	2:156097658	GGTCATAGGTGGCAC[A/C]GAAGGGACTGGGGGA	266692
rs265137959	snp	C/T			downstream-variant-500B	Cpne1	Mm_Celera	2:156071671	CTTATACAGCAAACA[C/T]TGTACCCAGTGAGCA	266692
rs265254937	snp	G/T			intron-variant	Cpne1	Mm_Celera	2:156075378	CAACAAGAGAATGAA[G/T]GTCCTGGATTTTAGG	266692
rs265351232	snp	A/C			intron-variant	Cpne1	Mm_Celera	2:156081778	TTAACAGCAGAAAGC[A/C]CCAAGAAACTCAATG	266692
rs265399645	snp	G/T			intron-variant	Cpne1	Mm_Celera	2:156082822	TTTAGAACCCTGGGA[G/T]AGCTTCCCAGTGCAT	266692
rs265502818	snp	A/T			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156105093	ATGTGCCATCATTTT[A/T]AAAAATAGCGATTTA	266692
rs265546974	snp	A/T			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156105282	ATAAAATAAATCTTT[A/T]TAAAAAATTAATGAT	266692
rs265617563	snp	A/T			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156109402	AGCTAGCTTTAAACG[A/T]AAAACTCTGCAAACC	266692
rs265652410	snp	A/G			synonymous-codon, intron-variant	Rbm12, Cpne1	Mm_Celera	2:156097880	CATGCTTGGAGGAGC[A/G]GTTCCTACGCTGGCT	266692
rs265717716	snp	A/G			utr-variant-3-prime	Cpne1	Mm_Celera	2:156073111	GTAGCACCTTCCATC[A/G]TGTTCATAGTCAGCC	266692
rs265774312	snp	A/G			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156100764	CTGGCTTGCACAAGA[A/G]CCTGCACTCATGTGC	266692
rs265986088	snp	C/T			intron-variant	Cpne1	Mm_Celera	2:156088535	ATGGAATAGCTGGGG[C/T]CATAGAACCATAGAC	266692
rs266130021	snp	C/T			utr-variant-3-prime, intron-variant	Rbm12, Cpne1	Mm_Celera	2:156095239	AGCCAACCAATGCTC[C/T]GTGTTATAGAAACCA	266692
rs386849762	in-del	-/GTTC			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156105151	GCGCACTGACTGTTC[-/GTTC]CTCCAGAAGTCCTGA	266692
rs386857933	in-del	-/A			utr-variant-3-prime	Cpne1	Mm_Celera	2:156072901	AAAAAAGTAAAAAAA[-/A]TCAAGACTATACTCC	266692
rs386880810	in-del	-/TACA			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156099838	TCTCTCTCTCACACA[-/TACA]CACACAACATACAAA	266692
rs386943363	in-del	-/T			intron-variant	Cpne1	Mm_Celera	2:156092483	TACGCTACACTAAGT[-/T]ATTACTCTCTGTAAG	266692
rs386954401	snp	A/G			intron-variant	Cpne1	GRCm38.p3	2:156085026	CTTCAGATGGCTCAG[A/G]CTGTCCTCCTGCCTT	266692
rs386967386	in-del	-/CA			utr-variant-3-prime	Cpne1	Mm_Celera	2:156072001	ATAAAAGCTCTAACA[-/CA]TACAGTTTGTGAACA	266692
rs386984090	snp	A/G			upstream-variant-2KB	Rbm12, Cpne1	GRCm38.p3	2:156112391	AACCAAAAAAGAAAG[A/G]AAGAAAGAAAGAAAG	266692
rs387011828	in-del	-/A			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156107898	TCTATTAAAAAAAAA[-/A]GTGATAGGAGAAGGC	266692
rs387044900	in-del	-/TGTGAAGAACAGGAA			intron-variant	Cpne1	Mm_Celera	2:156083435	ATGGACAGCAAGCTA[-/TGTGAAGAACAGGAA]CCCTACTTATAACAG	266692
rs387056749	in-del	-/GGGATTAAGTTAGACCTAAAAT			intron-variant	Cpne1	Mm_Celera	2:156074351	GACCTTAGACCTCAT[-/GGGATTAAGTTAGACCTAAAAT]CAGCCCATCTTGGCT	266692
rs387060511	snp	A/G			intron-variant	Cpne1	GRCm38.p3	2:156080584	TGAACACCACCTCCC[A/G]TCAGTTCTCTCAAGA	266692
rs387061985	in-del	-/T			utr-variant-3-prime	Cpne1	Mm_Celera	2:156073193	TCAAACTTTGTCTTT[-/T]CAAAGTATGTGACTG	266692
rs387142939	in-del	-/TT			intron-variant	Cpne1	Mm_Celera	2:156086796	GCCCCTCATTTTTTT[-/TT]ATGTTCTTTTCCCAG	266692
rs387173173	in-del	-/CTAAGCTGCGTGGG			downstream-variant-500B	Cpne1	Mm_Celera	2:156071773	TAAATACATGCAAAG[-/CTAAGCTGCGTGGG]AAAGCCCGACTCCAG	266692
rs387200946	in-del	-/A			intron-variant	Cpne1	Mm_Celera	2:156092996	GTTCTGGAAAAAAAA[-/A]TTGTCTGACGAGAGG	266692
rs387241193	in-del	-/GACA			utr-variant-3-prime	Cpne1	Mm_Celera	2:156072027	AACAGGTTACTGAGA[-/GACA]AGGAAATGTGTATGA	266692
rs387265855	in-del	-/A			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156099967	CAGCTCCAGGAAAAA[-/A]GGAGCGCCCTTTCCT	266692
rs387327297	in-del	-/ACCCGAG			intron-variant	Cpne1	Mm_Celera	2:156074635	TGCACAAGCCCAGAG[-/ACCCGAG]CTACATCCACAAACC	266692
rs387342152	in-del	-/TTT			utr-variant-3-prime	Cpne1	Mm_Celera	2:156073263	AGACCAAAGGGATCT[-/TTT]ACTCAACAAGCCCAA	266692
rs387346034	in-del	-/A			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156105662	ACAATTAAAAAAAAA[-/A]TCCCAAGTATTATTC	266692
rs387392367	in-del	-/TTACAACATGACCAA			intron-variant	Cpne1	GRCm38.p3	2:156087467	TTATTAAAGGTCCAA[-/TTACAACATGACCAA]GTCCAAGTTCTTCTA	266692
rs387400887	snp	A/G			upstream-variant-2KB	Rbm12, Cpne1	GRCm38.p3	2:156112520	AGAAAGAAAGAAAGA[A/G]AGAGAAAGAAAGAGA	266692
rs387404075	in-del	-/C			utr-variant-3-prime	Cpne1	Mm_Celera	2:156073143	CAGTTCAGCTCGCCC[-/C]GGAGGAAAGGACAAC	266692
rs387425685	in-del	-/N			intron-variant	Cpne1	Mm_Celera	2:156090819	AAAAAATAACTATTT[-/N]TTTAACATGAAAAGG	266692
rs387450890	in-del	-/CCTTGA			cds-indel	Cpne1	Mm_Celera	2:156072628	CCAGCTACTCCAGGA[-/CCTTGA]GTTGTAAAATGTAAA	266692
rs387524151	in-del	-/TTTTTT			intron-variant	Cpne1	Mm_Celera	2:156084602	TTTTTTTTTTTTTTT[-/TTTTTT]CTGCTCAGATTTCCT	266692
rs387565075	in-del	-/TG			downstream-variant-500B	Cpne1	Mm_Celera	2:156071571	CTGAGGACAACTCTG[-/TG]GAGCTAGTTCTCTCT	266692
rs387567394	in-del	-/T			utr-variant-3-prime	Cpne1	Mm_Celera	2:156071887	ATAGATATATTTTTT[-/T]AAAAGGGTAACATAT	266692
rs387605146	in-del	-/TC			intron-variant	Cpne1	Mm_Celera	2:156090867	AGATCCTACCATATC[-/TC]CTTAAGGAAAAAAAA	266692
rs387664945	snp	A/G			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156110233	AACATAAAATTATAC[A/G]TTACAATCCACAGTG	266692
rs387666927	in-del	-/TCC			cds-indel	Cpne1	Mm_Celera	2:156073510	ATTGGAGCCTACTCC[-/TCC]ACGGGTGCCTATGCC	266692
rs387698694	in-del	-/A			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156099508	TCATAAAGCTCAAAA[-/A]CCCACCCCCAGCACC	266692
rs387737970	in-del	-/CCT			intron-variant	Cpne1	Mm_Celera	2:156088267	TATACTAACTGTTCT[-/CCT]TTAGTGCTCACAGGT	266692
rs387753419	in-del	-/A			intron-variant	Cpne1	Mm_Celera	2:156075906	GGGTCTTCACAAAAA[-/A]CGGCCTGGGAAGCTC	266692
rs387770553	in-del	-/AGCTACATG			upstream-variant-2KB	Rbm12, Cpne1	Mm_Celera	2:156113077	ATCTTAAATTCTATG[-/AGCTACATG]GAGTGGCTCACAACC	266692
rs387829807	in-del	-/A			intron-variant	Rbm12, Cpne1	Mm_Celera	2:156107238	AAAAGGGGGGGGGGA[-/A]GAAATGTTGAAAGCC	266692
rs387839116	in-del	-/T			utr-variant-3-prime	Cpne1	Mm_Celera	2:156073175	ACAAGTTTACTTAAT[-/T]ATTCAAACTTTGTCT	266692
rs387890744	in-del	-/AA			intron-variant	Cpne1	Mm_Celera	2:156086053	TCTGGGGGAAAAAAA[-/AA]TATCCACTATTTTAT	266692
rs387898476	in-del	-/A			downstream-variant-500B	Cpne1	Mm_Celera	2:156071694	GTGAGCAACTTGCAA[-/A]TGTCCCCTCTATGCT	266692
rs578349716	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156088912	GAACTTCTGCTTTCA[C/T]CTTAACCTGTTACAA	266692
rs578477027	snp	A/G			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156102653	CTGGGAAAAAAAAAA[A/G]AAAAGAAAAAAAAAG	266692
rs578843734	snp	A/G			upstream-variant-2KB	Rbm12, Cpne1	GRCm38.p3	2:156112475	AAGAAAGAAAGAAAG[A/G]AAGAAAGAAAGAAAG	266692
rs578911157	snp	G/T			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156103987	GAGATTTATTTGAAC[G/T]TAATTCCCCAAAAAA	266692
rs578968969	snp	A/G			intron-variant	Cpne1	GRCm38.p3	2:156083377	TTCACCCACAGGATT[A/G]AGCCCATTCTCCAGC	266692
rs579005687	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156090357	GCTGAGTTTTATGTC[C/T]TAACCTTTAACGAAC	266692
rs579432142	snp	A/G			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156102708	GAAAAGAAAAGAAAA[A/G]AAAAGAAAAGAAAAG	266692
rs579455514	snp	C/T			missense, intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156096125	TATTGCGGGACCGGG[C/T]ATTGCGGGACCGGGC	266692
rs579525593	snp	A/G			upstream-variant-2KB	Rbm12, Cpne1	GRCm38.p3	2:156112530	AAAGAAAGAGAAAGA[A/G]AGAGAGAGAAAGAAA	266692
rs579550207	snp	G/T			intron-variant	Cpne1	GRCm38.p3	2:156087016	GTCATGGTACAGAAG[G/T]AGCAGGGCCCACAAG	266692
rs579601312	snp	A/G			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156107511	TCAAAAAAAAGTATT[A/G]TTATACAGGTATGGA	266692
rs579963878	snp	A/T			intron-variant	Cpne1	GRCm38.p3	2:156093705	AAGACCATCGCAGTA[A/T]TGGAGAGGCTTTCCA	266692
rs579998213	snp	A/C			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156108264	GAGGCAGGCGGATTT[A/C]TGAGTTCGAGGCCAG	266692
rs580046236	snp	A/G			upstream-variant-2KB	Rbm12, Cpne1	GRCm38.p3	2:156113380	AGAGAGAGAGAGAGC[A/G]CATGCGCGCGGGCAA	266692
rs580115601	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156075133	ACACACACACACACA[C/T]GAGGTTATAGAACCT	266692
rs580153369	snp	A/G			upstream-variant-2KB	Rbm12, Cpne1	GRCm38.p3	2:156112943	GAGAGAGAAAGGAAG[A/G]AAGGAAGGAAGGAAG	266692
rs580156233	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156086784	GAAAAATTATGTGCC[C/T]CTCATTTTTTTTTAT	266692
rs580522237	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156084577	GTTCAAAAAGGTTCC[C/T]ATGTTTTTTTTTTTT	266692
rs580587321	snp	C/T			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156108240	TTTAATCCCAGCACT[C/T]GGGAGGCAGAGGCAG	266692
rs580626573	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156080181	ACACCGTAATTCTAG[C/T]TCTCGGGGAAACACA	266692
rs580713933	snp	A/G			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156102663	AAAAAAAAAAGAAAA[A/G]AAAAGAAAAGAAAAG	266692
rs581106061	snp	C/G			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156102436	TGGAGTGTCTGAAGA[C/G]AGCTACAGTGTACTT	266692
rs581112481	snp	C/T			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156108333	CAGAGAGAAACCCTG[C/T]CTCAAAAAAAAAAAA	266692
rs581260786	snp	A/C			intron-variant	Cpne1	GRCm38.p3	2:156088052	CACCTGACATCCTTC[A/C]GTCGAGGGAGGAGGC	266692
rs581363468	snp	A/G			synonymous-codon, intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156096182	GGGCATTGCGGGACC[A/G]GGCATTGCGGGACCA	266692
rs581500766	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156083352	GCTCCCACTGGGCTG[C/T]TCTTTCTGATTCACC	266692
rs581775084	snp	A/G			intron-variant	Cpne1	GRCm38.p3	2:156084881	CTTTAAATTATCTGT[A/G]ATCTGTAGCTTTTCA	266692
rs581791218	snp	G/T			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156111459	CCACTAAGCGTGCAG[G/T]CGTTTTCATCGCAAT	266692
rs581821225	snp	A/C			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156107542	TGTTCTGCCTAGATA[A/C]TGCATATCTGTGTAT	266692
rs582227906	snp	A/G			upstream-variant-2KB	Rbm12, Cpne1	GRCm38.p3	2:156112516	AGAAAGAAAGAAAGA[A/G]AGAAAGAGAAAGAAA	266692
rs582230310	snp	A/G			upstream-variant-2KB	Rbm12, Cpne1	GRCm38.p3	2:156112467	AAGAAAGAAAGAAAG[A/G]AAGAAAGAAAGAAAG	266692
rs582234059	snp	C/T			utr-variant-3-prime	Cpne1	GRCm38.p3	2:156072652	GTAAAATGTAAAAGG[C/T]AGTCTGGGCAAAGTG	266692
rs582346916	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156083445	AAGCTACCCTACTTA[C/T]AACAGACACTCAGTA	266692
rs582604530	snp	A/G			intron-variant	Cpne1	GRCm38.p3	2:156085158	GAGGCTTTCATTTCA[A/G]CTTCCCTGAATATCA	266692
rs582693144	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156074763	CTAACCCACAAAGTT[C/T]TAGGCCATCCTAGCC	266692
rs582840968	snp	A/G			upstream-variant-2KB	Rbm12, Cpne1	GRCm38.p3	2:156112556	AGAAAAGAAAGAAAG[A/G]AAGAAAGAAAAAGGA	266692
rs582845951	snp	A/G			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156102733	GAAAAGAAAAGAAAA[A/G]AGAAAAAAACCTTAA	266692
rs582943445	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156089043	CTTCTCCAGTGTGCA[C/T]GCTGCTCGGTCAGCA	266692
rs583153949	snp	C/T			downstream-variant-500B	Cpne1	GRCm38.p3	2:156071609	TTTACATGGCTCCTA[C/T]GAGTAGAATTTACAT	266692
rs583155970	snp	A/C			downstream-variant-500B, intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156094393	TACCACTTTCATTTC[A/C]GTTTTATACTCCGAA	266692
rs583227350	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156087032	AGCAGGGCCCACAAG[C/T]AGTAGGTCAGTCTCT	266692
rs583380758	snp	C/T			upstream-variant-2KB	Rbm12, Cpne1	GRCm38.p3	2:156113383	GAGAGAGAGAGCGCA[C/T]GCGCGCGGGCAAATA	266692
rs583413193	snp	C/T			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156108286	CGAGGCCAGCCTGGT[C/T]TATAGAGTGAGTTCC	266692
rs583492186	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156086785	AAAAATTATGTGCCC[C/T]TCATTTTTTTTTATG	266692
rs583531304	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156076498	AGCTTTACCAACAAA[C/T]AAACAAACAAACAAA	266692
rs583622229	snp	A/G			upstream-variant-2KB	Rbm12, Cpne1	GRCm38.p3	2:156113319	GTGTGTGTGTGCGAG[A/G]GAGAGAGAGAGAGAG	266692
rs583900963	snp	C/G			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156101655	GTTACACTGCAGACC[C/G]AACCAGAGCTTTGTT	266692
rs583995568	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156087807	CTTTATAGTAGAAAA[C/T]CTAGCCCAGAGAGAA	266692
rs584005160	snp	A/G			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156108241	TTAATCCCAGCACTC[A/G]GGAGGCAGAGGCAGG	266692
rs584134108	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156088886	AGAAAGCAGCTATCT[C/T]CGAGGATAGTGAACT	266692
rs584252071	snp	C/T			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156102610	GAGTGAGTTCCAGGA[C/T]AGCCAGGGCTACATT	266692
rs584360187	snp	A/G			intron-variant	Cpne1	GRCm38.p3	2:156088888	AAAGCAGCTATCTTC[A/G]AGGATAGTGAACTTC	266692
rs584462738	snp	C/T			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156109311	ATAAATTTTTATTCA[C/T]TTATACTTCAAAATA	266692
rs584548796	snp	A/G			upstream-variant-2KB	Rbm12, Cpne1	GRCm38.p3	2:156112471	AAGAAAGAAAGAAAG[A/G]AAGAAAGAAAGAAAG	266692
rs584562775	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156084575	CTGTTCAAAAAGGTT[C/T]CCATGTTTTTTTTTT	266692
rs584673921	snp	A/G			intron-variant	Cpne1	GRCm38.p3	2:156088385	ACAGGCTAGAAAACA[A/G]TGACTCTCTTCTGAG	266692
rs584800510	snp	C/T			upstream-variant-2KB	Rbm12, Cpne1	GRCm38.p3	2:156112249	CAAAAGCTTGAACCT[C/T]TTTTTGACTATTGAA	266692
rs584907795	snp	A/G			intron-variant	Cpne1	GRCm38.p3	2:156080371	AGCACCTACACTGGC[A/G]GCTTCCAACAGTCTG	266692
rs584945961	snp	C/T			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156103191	TATACATAAATAAAA[C/T]AGACTCTCAGGAAAC	266692
rs585063902	snp	A/G			intron-variant	Cpne1	GRCm38.p3	2:156086048	TCTCCTCTGGGGGAA[A/G]AAAAAATATCCACTA	266692
rs585079968	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156083362	GGCTGTTCTTTCTGA[C/T]TCACCCACAGGATTG	266692
rs585230068	snp	A/G			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156102693	GAAAAGAAAAGAAAA[A/G]AAAAGAAAAGAAAAG	266692
rs585331985	snp	A/G			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156104156	CGTCTCACAAAAAAA[A/G]TATTTTTCCAGCAAA	266692
rs585526583	snp	A/G			missense, intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156096088	CACCAGGTATTGCGG[A/G]ACCAGGTATTGCGGG	266692
rs585551842	snp	C/T			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156108232	CGCACGCCTTTAATC[C/T]CAGCACTCGGGAGGC	266692
rs585874766	snp	A/G			upstream-variant-2KB	Rbm12, Cpne1	GRCm38.p3	2:156112922	AGAGAGAGAGAGAGA[A/G]AGAGAGAGAGAGAAA	266692
rs586084993	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156093157	CCAGAGGGCAGAGCA[C/T]TTAGTTACATTTCAC	266692
rs586183285	snp	A/G			intron-variant	Cpne1	GRCm38.p3	2:156085168	TTTCAGCTTCCCTGA[A/G]TATCACAGCAAGGTG	266692
rs586227950	snp	A/G			intron-variant	Cpne1	GRCm38.p3	2:156074848	AGGACAAAGAATTTG[A/G]TTTAAATATATATGT	266692
rs586236144	snp	A/G			intron-variant	Cpne1	GRCm38.p3	2:156087458	CAAGAGCTGTTATTA[A/G]AGGTCCAATTACAAC	266692
rs586287690	snp	A/G			intron-variant	Cpne1	GRCm38.p3	2:156089143	AGGATGATTTTAAGT[A/G]CCAGCCTTTAAAAGT	266692
rs586427076	snp	C/T			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156108329	GCTACAGAGAGAAAC[C/T]CTGCCTCAAAAAAAA	266692
rs586709930	snp	A/G			upstream-variant-2KB	Rbm12, Cpne1	GRCm38.p3	2:156113390	AGAGCGCATGCGCGC[A/G]GGCAAATAAGAGGGA	266692
rs586717457	snp	A/G			intron-variant	Cpne1	GRCm38.p3	2:156079542	TCCCAGCCTGGGAAA[A/G]CTGCATACTGCACAC	266692
rs586791750	snp	A/G			intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156102377	AATCCCAGCAACCAC[A/G]TGGTGGCTCACAACC	266692
rs587052461	snp	A/G			utr-variant-3-prime	Cpne1	GRCm38.p3	2:156071897	TTTTTTAAAAGGGTA[A/G]CATATATAAAAATAA	266692
rs587201495	snp	A/C			intron-variant	Cpne1	GRCm38.p3	2:156076511	AATAAACAAACAAAC[A/C]AACAAAAAGAAAAAA	266692
rs587220767	snp	A/G			upstream-variant-2KB	Rbm12, Cpne1	GRCm38.p3	2:156113362	AGAGAGAGAGAGAGA[A/G]AGAGAGAGAGAGAGA	266692
rs587390596	snp	C/T			intron-variant	Cpne1	GRCm38.p3	2:156088046	CAGCCTCACCTGACA[C/T]CCTTCCGTCGAGGGA	266692
rs587469209	snp	A/G/T			synonymous-codon, intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156096152	GGGCATTGCGGGACC[A/G/T]GGCATTGCGGGACCG	266692
rs864267563	snp	A/G			intron-variant	Cpne1	GRCm38.p3	2:156092771	CCAAAAGAAAAATAA[A/G]CACTAATAAAAACTC	266692
rs864271776	snp	A/T			intron-variant	Cpne1	GRCm38.p3	2:156093603	AGCAAATTGTGTTTG[A/T]GAGTTATCAAGTGAT	266692
rs864284134	snp	A/T			downstream-variant-500B, intron-variant	Rbm12, Cpne1	GRCm38.p3	2:156094583	ATGAACAAATTTTAA[A/T]CTCCCTAAACTAAAT	266692

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