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

Trim12a

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs31922156	snp	A/G	0.244898	0.249948	utr-variant-3-prime	Trim12a	Mm_Celera	7:104299987	CCTTCTTGCTGAGTG[A/G]AATCTTCCCTTAACA	76681
rs31922158	snp	C/T	0.336735	0.234472	utr-variant-3-prime	Trim12a	Mm_Celera	7:104300124	TGCATTGCCATCTAT[C/T]GGTGGCCTAGAGTTT	76681
rs31922160	snp	G/T	0.444444	0.157135	intron-variant	Trim12a	Mm_Celera	7:104300405	AAGGAGAGACTTCAA[G/T]CAGTGACAGTTAGGA	76681
rs31922163	snp	A/T	0.5	0	intron-variant	Trim12a	GRCm38.p3	7:104300869	CTGTGACCTCTGAAA[A/T]GGGGTAAAAATTTAC	76681
rs31922675	snp	A/C	0.5	0	intron-variant	Trim12a	GRCm38.p3	7:104304591	GAAGCCTGCTTCATC[A/C]TCTTCTTGTATGGGA	76681
rs31922678	snp	C/T	0.444444	0.157135	intron-variant	Trim12a	GRCm38.p3	7:104304595	cctgcttcatcatct[C/T]cttgtatgggaatgg	76681
rs31922680	snp	G/T	0.444444	0.157135	intron-variant	Trim12a	GRCm38.p3	7:104304646	CTCTTAGGGAATCTT[G/T]GATAGCCTTTTAGTG	76681
rs31922683	snp	G/T	0.142012	0.225474	intron-variant	Trim12a	GRCm38.p3	7:104304694	AACACACAGACCTCT[G/T]GTCAGCTTTCCTCAG	76681
rs31923026	snp	C/T	0.48	0.0979796	intron-variant	Trim12a	GRCm38.p3	7:104300991	AACAGTCATTTCCCA[C/T]CTGAGATGGTTATAT	76681
rs31923029	snp	A/T	0.46875	0.121031	intron-variant	Trim12a	GRCm38.p3	7:104301004	CACCTGAGATGGTTA[A/T]ATCACCAGTAGCTGG	76681
rs31923174	snp	C/T	0.32	0.24	upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316846	GAACCACGGTCCTTG[C/T]GGATGCTGGGCTAGT	76681
rs31923176	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316917	TGATGAGGTCATAAG[C/T]CTCACTGTTGTTCTT	76681
rs31923179	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316979	TTGATGTTCCCATTC[C/T]TCTGAAATGTTAATA	76681
rs31923182	snp	A/T	0.444444	0.157135	upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104317081	GGCTAGAAATCACTA[A/T]GTGTTTAGAGTGTTT	76681
rs31923915	snp	C/T	0.244898	0.249948	intron-variant	Trim12a	GRCm38.p3	7:104305650	GCATAAGCCATCATA[C/T]GTGCCATTACATTCT	76681
rs31923918	snp	A/G	0.132653	0.220748	intron-variant	Trim12a	GRCm38.p3	7:104305687	AACTCCCTGGCAGAA[A/G]TTAAACACTGATCAC	76681
rs31923920	snp	C/G	0.165289	0.235211	intron-variant	Trim12a	GRCm38.p3	7:104305745	ATCTTCTTCTGTAGA[C/G]TCAGTTTCAGAAGGC	76681
rs31923923	snp	C/T	0.32	0.24	intron-variant	Trim12a	GRCm38.p3	7:104305796	TCCCTTCTGACCAAG[C/T]ATCCTCTGTGGTGCC	76681
rs31924285	snp	C/T	0.32	0.24	upstream-variant-2KB, nc-transcript-variant	Trim12a, Gm15133	Mm_Celera	7:104317306	GGCAGAATTCCACTC[C/T]CAACTCTGCAAAGAT	76681
rs31924288	snp	C/T	0.444444	0.157135	upstream-variant-2KB, nc-transcript-variant	Trim12a, Gm15133	Mm_Celera	7:104317346	CATTTAGTCTGCCAT[C/T]ACCCTCTGACCTCAG	76681
rs31924291	snp	C/T	0.375	0.216506	upstream-variant-2KB, nc-transcript-variant	Trim12a, Gm15133	Mm_Celera	7:104317349	TTAGTCTGCCATTAC[C/T]CTCTGACCTCAGTGA	76681
rs31924802	snp	C/G	0.124444	0.216185	intron-variant	Trim12a	GRCm38.p3	7:104301577	CTTCAAAATGCTTAG[C/G]CAATATGGAGACTCA	76681
rs31924865	snp	C/T	0.42	0.183303	missense, intron-variant	Trim12a	GRCm38.p3	7:104306049	TCCAGTTTTCAAATT[C/T]TTTCTTATCTGCCAT	76681
rs31924868	snp	A/G	0.142012	0.225474	intron-variant	Trim12a	Mm_Celera	7:104306212	CTACCTTTCTTTTAA[A/G]GGATTGTGATATGAA	76681
rs31924871	snp	C/T	0.152778	0.230321	intron-variant	Trim12a	Mm_Celera	7:104306355	TTGGTCTGGGAAGTT[C/T]ACAGAAACCCAGGAA	76681
rs31925064	snp	G/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Gm15133, Trim12a	Mm_Celera	7:104317502	ATTCCCATGGAACAC[G/T]ATTTGAGAGGAAATA	76681
rs31925069	snp	A/G	0.48	0.0979796	intron-variant, upstream-variant-2KB	Gm15133, Trim12a	Mm_Celera	7:104317619	AACACTTGTGAGTTT[A/G]TACTCCAGGTATTCT	76681
rs31925072	snp	A/G	0.5	0	nc-transcript-variant, upstream-variant-2KB	Gm15133, Trim12a	Mm_Celera	7:104317660	CCAAAGCATGGCCAC[A/G]GTTTTGAATGGGCTG	76681
rs31925665	snp	A/T	0.48	0.0979796	intron-variant	Trim12a	GRCm38.p3	7:104301996	TGCAAGCACACAGGG[A/T]GAATTACAATAGAGT	76681
rs31925668	snp	G/T	0.444444	0.157135	intron-variant	Trim12a	Mm_Celera	7:104302632	ACACAAGGAGCTGAT[G/T]ACTGCAAGGGATAGT	76681
rs31925671	snp	C/T	0.444444	0.157135	intron-variant	Trim12a	Mm_Celera	7:104302637	AGGAGCTGATTACTG[C/T]AAGGGATAGTCTGAA	76681
rs31925754	snp	G/T	0.408163	0.193609	intron-variant	Trim12a	GRCm38.p3	7:104312521	AGATTCAATCAATTA[G/T]GAGACATGATCAAGC	76681
rs31925757	snp	A/T	0.48	0.0979796	intron-variant	Trim12a	GRCm38.p3	7:104312579	CACTTAAAAGAATCA[A/T]ACAAGCTGGCCGGTG	76681
rs31925760	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313087	TGAATACCATCACTC[C/T]TACAGTGTCATGTCA	76681
rs31925763	snp	A/C	0.375	0.216506	intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314086	TTGAGAAAGCAAAAC[A/C]CACAAAATCAACCTT	76681
rs31925915	snp	G/T	0.444444	0.157135	nc-transcript-variant, upstream-variant-2KB	Gm15133, Trim12a	Mm_Celera	7:104317723	TGGATTCTACTTGCT[G/T]CCGTGTAAGTACTCT	76681
rs31926354	snp	A/C	0.142012	0.225474	intron-variant	Trim12a	Mm_Celera	7:104302894	GTCTGTGACTTCTTC[A/C]GTTAGGCTTTGAGAC	76681
rs31926357	snp	C/T	0.124444	0.216185	intron-variant	Trim12a	Mm_Celera	7:104303911	CTGGTGTCATAAATG[C/T]CCATGGATCCAATAG	76681
rs31926360	snp	A/G	0.142012	0.225474	intron-variant	Trim12a	Mm_Celera	7:104303917	TCATAAATGCCCATG[A/G]ATCCAATAGATCTCC	76681
rs31926363	snp	A/G	0.132653	0.220748	intron-variant	Trim12a	Mm_Celera	7:104303972	TCTCTACAAATTCAT[A/G]AAAATAAAATTCCAC	76681
rs31926458	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314253	AGGTAGAAAGAGGCT[A/G]TTGCAGTCATGTGCT	76681
rs31926461	snp	C/T	0.48	0.0979796	intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314368	GAAACCTTACAAAAG[C/T]TGGCACTTTGGGGGA	76681
rs31927056	snp	C/G	0.124444	0.216185	intron-variant	Trim12a	Mm_Celera	7:104303993	AAAATTCCACTCCTT[C/G]TTATTTGTGCATGCA	76681
rs31927059	snp	A/C	0.297521	0.245442	intron-variant	Trim12a	Mm_Celera	7:104304015	GTGCATGCAGTGATC[A/C]TTCCAGCCTCTGAAA	76681
rs31927062	snp	A/G	0.124444	0.216185	intron-variant	Trim12a	Mm_Celera	7:104304057	AAGAGTTCAGGAAGA[A/G]CTCACTGTCATCACC	76681
rs31927239	snp	A/G	0.48	0.0979796	intron-variant, upstream-variant-2KB	Trim12a, Gm15133	Mm_Celera	7:104314702	TGTCAAACAGGGTCG[A/G]TGACTAAATAACAGG	76681
rs31927242	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Trim12a, Gm15133	Mm_Celera	7:104314728	ACAGGCTCTCAGTCT[C/T]TGTTACTAAACTGAG	76681
rs31927835	snp	C/G	0.336735	0.234472	intron-variant	Trim12a	GRCm38.p3	7:104304088	AGGAAGACCACAGCA[C/G]CAGAGAGGAAGGGCA	76681
rs31927838	snp	C/T	0.132653	0.220748	intron-variant	Trim12a	GRCm38.p3	7:104304111	GAAGGGCAATGGCTT[C/T]CATGCCTTCTGACTC	76681
rs31927841	snp	A/G	0.124444	0.216185	synonymous-codon	Trim12a	GRCm38.p3	7:104304204	ATGTTCCACATCTGA[A/G]ATGAAGTCTTCTAGC	76681
rs31928095	snp	A/C	0.444444	0.157135	intron-variant, nc-transcript-variant	Trim12a, Gm15133	Mm_Celera	7:104315087	TGTCATAGACAACAA[A/C]GTTCTGGATCTCGTC	76681
rs31928098	snp	G/T	0.444444	0.157135	intron-variant	Trim12a, Gm15133	Mm_Celera	7:104315113	TCGTCGACAAGGTAC[G/T]ATTCAAAATTACAGA	76681
rs31928101	snp	A/G	0.444444	0.157135	intron-variant	Trim12a, Gm15133	Mm_Celera	7:104315305	GATAAACTCACCCAA[A/G]CAAAAGCAATGTTCT	76681
rs31928744	snp	C/T	0.244898	0.249948	missense	Trim12a	GRCm38.p3	7:104304244	TGCTGAGCATGCTCA[C/T]TTTCAGACTCTGCCA	76681
rs31928747	snp	A/G	0.244898	0.249948	missense	Trim12a	GRCm38.p3	7:104304269	CTGCCAGGTTGTTGA[A/G]AATGTCTTCCTTCTC	76681
rs31928749	snp	C/T	0.375	0.216506	missense	Trim12a	GRCm38.p3	7:104304275	GGTTGTTGAGAATGT[C/T]TTCCTTCTCTTGCCT	76681
rs31928751	snp	C/T	0.5	0	missense	Trim12a	GRCm38.p3	7:104304323	TCTTCTCCTCAGAGT[C/T]CATGATATCCCTCAT	76681
rs31928753	snp	C/T	0.5	0	missense	Trim12a	GRCm38.p3	7:104304355	CGTTTAAACTCTGAC[C/T]GAACATTCTGCACAT	76681
rs31928824	snp	A/G	0.444444	0.157135	intron-variant	Trim12a, Gm15133	Mm_Celera	7:104315340	TCAAAGTCTTCAAAA[A/G]TCTGCCCCCTAAAAT	76681
rs31929522	snp	G/T	0.244898	0.249948	downstream-variant-500B	Trim12a	Mm_Celera	7:104299855	CTAGATAAAAATACC[G/T]CTGCTGTCTGGCCTG	76681
rs31929661	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316771	TCCCTTAGCCTCCCC[A/G]GTGCTGGGATCATGA	76681
rs31929663	snp	G/T	0.444444	0.157135	upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316811	GTTGTTGTTCAGTTT[G/T]GCTTTTGACTTCAGT	76681
rs31929956	snp	A/G	0.152778	0.230321	intron-variant	Trim12a	GRCm38.p3	7:104304410	ATAAGAAAAGGGAGA[A/G]CCATTAAGTTTGTCA	76681
rs31930285	snp	C/G	0.18	0.24	utr-variant-3-prime	Trim12a	Mm_Celera	7:104299924	TTGTTTTATTTTCGG[C/G]TCACACATTAATAAA	76681
rs31930288	snp	A/G	0.46281	0.131194	utr-variant-3-prime	Trim12a	Mm_Celera	7:104299931	ATTTTCGGGTCACAC[A/G]TTAATAAAAGTTTCT	76681
rs31930291	snp	C/G	0.277778	0.248452	utr-variant-3-prime	Trim12a	Mm_Celera	7:104299948	TAATAAAAGTTTCTC[C/G]TGTTTCTTTTGAGTT	76681
rs211712734	snp	C/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316274	TCAAGAATGCCACAC[C/T]CCTAATCTTTCCTGA	76681
rs211751499	snp	G/T			utr-variant-3-prime, missense	Trim12a	Mm_Celera	7:104300305	CCACTTCTGCCTGGA[G/T]GAAAGATCTCCCCTT	76681
rs211992562	in-del	-/TTC			cds-indel	Trim12a	GRCm38.p3	7:104301138	CAGGGGCTCGGAACT[-/TTC]TTCTTTGTTCCCTGG	76681
rs212078216	snp	G/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313473	ACACTCCCAAAGACA[G/T]CGGCATACGCATGGA	76681
rs212312591	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104310306	ATAGCTGGGCCTTGA[C/G]GTAGATCAATTCCCA	76681
rs212678214	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309754	CACTAGGGTCATCCT[C/T]ATAGATTCCAGAAAG	76681
rs212876991	snp	G/T			missense	Trim12a	Mm_Celera	7:104307151	TGCTAAACTGGTAAC[G/T]AATTCGGCACACAGG	76681
rs213052059	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104308119	CCTGCCTCTGCCTCC[C/G]AAGTGCTGGGTTTAA	76681
rs213196247	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309974	acctttctgggtctc[C/T]ggattatagttcaat	76681
rs213360521	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104308765	AACCCAGTAGCTGAC[C/T]CAGATAGGTACAGAC	76681
rs213469132	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104311440	TTGAATCTGTAGATT[C/G]CTTTTGCTAGGATGA	76681
rs213940468	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104310334	CCAGTTTTGTGAGGA[A/G]CAGACATATTGATTT	76681
rs214022401	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104309049	AAGCTGTTGTTCTAT[G/T]TGCTGGGCTGCCTTG	76681
rs214046500	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104307474	cacctccatgagatt[A/C]ccgaaccatacaggt	76681
rs214250301	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301971	TGTTAAATCCAGATC[C/T]ACAGCCACATGCAAG	76681
rs214600454	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104301676	AACTAAGACTAATAT[A/C]TTCCCAGTGTCTCAG	76681
rs214771022	snp	C/G			intron-variant	Trim12a	Mm_Celera	7:104303307	gaatttataagccag[C/G]cgcaattaaatgtcc	76681
rs215340827	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104302023	GAGTTAAGAGTACCC[C/T]AATTTTTTAATCCCT	76681
rs215928680	snp	C/G			intron-variant	Trim12a	Mm_Celera	7:104300690	TACAGGCACTGGAGA[C/G]AACTTTGTGCAGAAG	76681
rs216208660	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104307944	aaagaggaaatggat[A/C]aattccttaaagaaa	76681
rs216404109	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301521	AAAAGTGTGTGGAAA[A/G]TATTCACATGAATGT	76681
rs216416382	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104305957	TTGCCAAGGTCCCTC[C/T]TGGGCATCAGGTTGA	76681
rs216472497	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104305530	gtacctacctagacc[A/C]ggttttaccttgtag	76681
rs217171792	snp	A/G			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104317178	AGCTACCATGTCTCT[A/G]TCTTTTCTACATTTT	76681
rs217656564	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301723	AGCTTGGTGTGCCCT[A/G]TGGACACAAGGATAC	76681
rs217721583	snp	C/T			intron-variant	Trim12a	Mm_Celera	7:104303127	ggccttgtaggtctg[C/T]cactgcgggcatggg	76681
rs217821303	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104310430	CTTCACCAACATTAG[A/C]TGTCACTTTTGTTAT	76681
rs217944221	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104312758	AACCAAACAAACAAA[A/C]AAAAAAGAATCATAC	76681
rs217963401	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301592	CCAATATGGAGACTC[A/G]CAAATAACATCTGAT	76681
rs218112553	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301885	CAATGTCTTCTAGCC[C/T]CAGAAGAAAATAGTG	76681
rs218365640	snp	A/G			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316956	CACAATTGCTTACAA[A/G]TAATGCTTTGATGTT	76681
rs218575388	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104312133	agaatcagagccatc[A/G]tacctaattaagtgc	76681
rs218908406	snp	A/G			intron-variant	Trim12a	Mm_Celera	7:104302494	aataaaaaaagaaaa[A/G]aaaagaaaagaaaaa	76681
rs219057059	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104305898	GGAGTATCAAGGTTT[A/C]TTGGCCTCATAAACT	76681
rs219556992	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309285	TTGTGGCATGGGGAA[A/G]CACAAGTCTATGTCT	76681
rs219561333	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104305586	GTACACAAGACCAGT[A/C]TTTAACTTACAGATA	76681
rs219565471	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309603	TGTCCTAGCATCAGC[C/T]TGGGCTTTTTAGGGA	76681
rs219639012	snp	A/G			intron-variant	Trim12a	Mm_Celera	7:104306426	ACTAAATATCTACTC[A/G]GAAAATGATTCCCCA	76681
rs219660153	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104308485	catccaggaaatctg[G/T]gaaaccatgaaaaga	76681
rs219691982	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104307575	AGCCTGTTAGCCCAG[A/G]GAGATCTCCATTCTC	76681
rs219794600	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104310179	CCACACTTTATGACA[A/T]CTAGGTTGTTTCCAG	76681
rs220217862	snp	C/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	Trim12a, Gm15133	Mm_Celera	7:104315554	TGACTGAGGAAGTTA[C/T]CCTCATATCAGCATT	76681
rs220250119	snp	A/G			utr-variant-3-prime, missense	Trim12a	Mm_Celera	7:104300380	CATGGCGGAGGGAGG[A/G]AGACCCTAAAAGGAG	76681
rs220309793	snp	A/C			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104317013	ATGAAAAACCCTTTA[A/C]CTTTTTTTTTTTTTT	76681
rs220400890	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104301874	AGAGAAAGATTCAAT[G/T]TCTTCTAGCCCCAGA	76681
rs220448858	snp	A/G			intron-variant	Trim12a	Mm_Celera	7:104300905	TAATTGCATGCAAAG[A/G]CACTGTAAAGTCCTT	76681
rs220652926	snp	A/T			intron-variant	Trim12a, Gm15133	Mm_Celera	7:104315114	CGTCGACAAGGTACG[A/T]TTCAAAATTACAGAT	76681
rs220792975	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309111	CAAGTGGGTGTCTAC[A/G]GCACACATGTGCCAT	76681
rs221004558	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104308152	CCATGCACCACCATT[G/T]CCCAGCCATATAGAG	76681
rs221048319	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104301712	CCCTGGTTGCCAGCT[G/T]GGTGTGCCCTGTGGA	76681
rs221401110	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104300954	GAAGAGTTGGAAACC[C/G]TAACAGGGTCCTTTA	76681
rs221537520	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104310513	TGCTTTTTCGTGATG[A/G]CTAAGAATGTTGAAC	76681
rs221600188	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104305174	TCAGGAGAGGATACT[A/G]GGACCTCCAGAACTA	76681
rs222303378	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104312787	ACAAACCCAATCAAC[C/T]AACCAACAACAACAA	76681
rs223630796	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309531	CTTTCAGTGAGCTGT[A/G]TGGATGTTGTCTTTG	76681
rs223658493	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310008	CATTTACTTAACAGG[C/T]AATATCCACATATAG	76681
rs223963352	snp	A/G			intron-variant	Trim12a	Mm_Celera	7:104303212	agatgaaaatgtaga[A/G]ctctcagttcctcct	76681
rs224156371	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104308639	cttacagaataccaa[C/T]tagattggagcagaa	76681
rs224157052	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104307459	ttctggcttcttctc[C/G]acctccatgagatta	76681
rs224209222	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309492	CTTTGCTCACTGCCA[A/G]GGGTGGTGGTGGGGA	76681
rs224466461	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104302097	TCTCTACCATAGAAT[C/G]TAATCTATTCTCAAT	76681
rs224472684	snp	A/G			intron-variant	Trim12a	Mm_Celera	7:104300511	AAATTGAGCAGAAAA[A/G]GTCTTTTTTTTTTTT	76681
rs224546691	snp	G/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104317043	TTTTTTGGAGGCAGA[G/T]ATTTACTCTATATTC	76681
rs224980838	snp	C/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	Mm_Celera	7:104314811	CTCTTTAGAAAACTT[C/T]CTCGTGTTGTATTGA	76681
rs225055503	snp	A/G			intron-variant	Trim12a	Mm_Celera	7:104300656	TCTTGGTTATTAATA[A/G]AAGGCTAAGAAGAAA	76681
rs225157652	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104312829	AAGACAAAAACAAAT[A/T]CCCTAATATACGCTA	76681
rs225438702	snp	A/C			downstream-variant-500B	Trim12a	Mm_Celera	7:104299806	CTAACACCTTTAATC[A/C]TTAAGGAAATCAGAG	76681
rs225677506	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104305794	TATCCCTTCTGACCA[A/C]GCATCCTCTGTGGTG	76681
rs225713860	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104308186	TTTTAAAAGGAAACA[A/G]ATAAATCTCTTAAAG	76681
rs225847757	snp	A/C/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104317137	ACTAATTTGTCAAAC[A/C/T]CTTGAGTTCAGGGAC	76681
rs225870297	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301391	CTTACATTCTCAGAA[C/T]CATGGTGCTTGCCCT	76681
rs225892051	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301775	ATAGGGTATGGGAAA[A/G]AAAAGGATAGTTGAT	76681
rs225992312	snp	C/T			stop-lost, synonymous-codon	Trim12a	Mm_Celera	7:104300838	AATTTTTACTTACCC[C/T]AGTAGCGATGAGCCT	76681
rs226233665	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104312882	ATCCATTTGTGTTGA[C/T]CAACTACTCCTGGGC	76681
rs226418591	snp	A/T			intron-variant	Trim12a	Mm_Celera	7:104300824	ATTAAGATGCTGCAA[A/T]TTTTTACTTACCCTA	76681
rs226578377	snp	A/T			intron-variant	Trim12a	Mm_Celera	7:104302867	CATATGCCTCACTTC[A/T]GTTTTGCTTTTGTCT	76681
rs226695937	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310409	AATTTTTCTCTTGCT[C/T]GACATCTTCACCAAC	76681
rs226873914	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104311347	GGTCTTTTTTTTTTC[C/T]TTTTTTTCCATATAA	76681
rs226925653	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104312908	TGGGCATGGGGCTTG[C/T]CTTGGAGGGTCATTG	76681
rs226985789	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309072	CTGCCTTGTCTGACC[A/G]CAGTGGGAGAGCAAG	76681
rs227096607	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309947	ACCTCCTAGAACTCT[C/T]CTCTGTATCTAACCT	76681
rs227257383	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104312096	acttaactgtatgaa[A/G]actctactgctgtac	76681
rs227680999	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310068	GTCTGTGTTACCTCA[C/T]CCAGGAAGGCTTTTT	76681
rs227909337	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104309591	AAAACCACCCTCTGT[C/G]CTAGCATCAGCTTGG	76681
rs228707405	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301886	AATGTCTTCTAGCCC[C/T]AGAAGAAAATAGTGT	76681
rs229234178	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104305784	AATGACCCAGTATCC[A/C]TTCTGACCAAGCATC	76681
rs229348781	in-del	-/ACAC			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316939	TTGTTCTTGCTGTGG[-/ACAC]ACACAATTGCTTACA	76681
rs229466342	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104307835	acctccaaagcacag[C/T]gcacccactgcagaa	76681
rs229524902	snp	C/T			missense	Trim12a	GRCm38.p3	7:104301160	GTTCCCTGGCGATGG[C/T]TTTGGGCTTCTTCAT	76681
rs229724476	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309766	CCTTATAGATTCCAG[A/G]AAGTTTCCACATCAC	76681
rs229749184	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104310308	AGCTGGGCCTTGAGG[A/T]AGATCAATTCCCAGT	76681
rs229831743	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309798	ccacaaatgccctct[A/G]attcaactgtctctc	76681
rs229998313	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104308161	ACCATTTCCCAGCCA[G/T]ATAGAGGTCTTTTAA	76681
rs230106136	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104308870	AGGATAGGAACTCCA[C/G]AGGAAGACCAACAGA	76681
rs230108380	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104310007	tcatttacttaacag[A/G]caatatccacatata	76681
rs230441104	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301747	AGGATACCTATCCTC[C/T]TCCTACACTCCCATA	76681
rs231008713	snp	C/T			utr-variant-3-prime	Trim12a	Mm_Celera	7:104299964	TGTTTCTTTTGAGTT[C/T]GTGGCTGCCTTCTTG	76681
rs231429171	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104305711	TGATCACATATCCAT[G/T]ACCCACCCATTCCCA	76681
rs231549459	snp	A/T			intron-variant	Trim12a	Mm_Celera	7:104303069	tatgcttggcccaac[A/T]aagtggcacttttag	76681
rs231615240	snp	A/G			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104317222	TCTGTTTCTTCCTAA[A/G]GTCTGTCTGGGAATT	76681
rs231653507	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301888	TGTCTTCTAGCCCCA[A/G]AAGAAAATAGTGTGA	76681
rs231709820	snp	C/T			intron-variant	Trim12a	Mm_Celera	7:104303605	cttttttaaaagatt[C/T]atttattttatgtat	76681
rs231791462	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104301849	TTTTTGTAAATCTAA[A/C]TATAACAACAGAGAA	76681
rs231932250	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301683	ACTAATATATTCCCA[A/G]TGTCTCAGGAAAACC	76681
rs231948652	snp	A/C			missense	Trim12a	Mm_Celera	7:104306963	TTTGTGACCACGGTG[A/C]TCCTGAGATCGCTCA	76681
rs231991272	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104302000	AGCACACAGGGTGAA[C/T]TACAATAGAGTTAAG	76681
rs232046355	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104312767	AACAAACAAAAAAGA[A/G]TCATACAAACCCAAT	76681
rs232075739	snp	A/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313776	AAGAGGGGAGCACAC[A/G]TCTCAGCAAATTCAG	76681
rs232176156	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104312941	ATACCCAGCAACACA[C/T]CATTGGAGAAACCTG	76681
rs232505919	snp	A/C			intron-variant	Trim12a, Gm15133	Mm_Celera	7:104315164	ACTAAATCTGGACAA[A/C]AGGCATCTTTAAAGT	76681
rs232899912	snp	A/T			intron-variant	Trim12a, Gm15133	Mm_Celera	7:104315204	TTGTTGTTGTTGTTG[A/T]GGAGGCACCTCCCTC	76681
rs232931106	snp	A/G			utr-variant-3-prime, missense	Trim12a	Mm_Celera	7:104300279	TAAAACCAGTCCCTG[A/G]CTTTTCTTCACCACT	76681
rs233484201	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310599	TAGATCTGTGCCTGT[C/T]TTTAATTGGATTATA	76681
rs233838843	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104307593	GATCTCCATTCTCCT[A/G]CCCACTCTCAGCCCA	76681
rs233876989	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309064	GTGCTGGGCTGCCTT[A/G]TCTGACCACAGTGGG	76681
rs234181733	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309935	ATATACATGCTTACC[C/T]CCTAGAACTCTCCTC	76681
rs234580910	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104312903	actcctgggcatggg[A/G]cttgtcttggagggt	76681
rs235177632	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104308439	CCTCAGTCAAAGAAA[A/T]TGTTAAAGCTAAAAC	76681
rs235722104	snp	C/G/T			intron-variant	Trim12a	GRCm38.p3	7:104309581	CTCTTCGTGGAAAAC[C/G/T]ACCCTCTGTCCTAGC	76681
rs235743129	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104312158	aagtgccacccttat[A/G]tggaatatataagtc	76681
rs236407121	snp	G/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104317116	TAGTTTCTAATTCCT[G/T]GGAATACTAATTTGT	76681
rs236719767	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104307547	TTCTGGGCCAAGCCA[A/T]GCTGCCCTAAGCAGC	76681
rs236895545	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309136	TGCCATGCACTGAAA[A/G]GCAGGTCTGTGGGTG	76681
rs237174010	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301624	TTTCAGGTTCTCTTG[A/G]AGAAATTCAAAACAG	76681
rs237252777	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301790	AAAAAGGATAGTTGA[C/T]CAAACCTGCATCAAA	76681
rs237258786	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104305909	GTTTATTGGCCTCAT[A/C]AACTCCCAGGAAGTA	76681
rs237297166	snp	C/T			intron-variant	Trim12a	Mm_Celera	7:104302701	taattgaggggcaga[C/T]aaagtgatgaataag	76681
rs237885319	snp	A/G			intron-variant	Trim12a	Mm_Celera	7:104300483	GTAAAAGAGTTCTAG[A/G]TTAATCGACTTGAAA	76681
rs238005866	in-del	-/TAA			intron-variant	Trim12a	GRCm38.p3	7:104301670	ACAACAAACTAAGAC[-/TAA]TATATTCCCAGTGTC	76681
rs238063636	snp	C/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	Mm_Celera	7:104314829	CGTGTTGTATTGACC[C/G]CAACCATAAAACTGT	76681
rs238127766	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104312902	TACTCCTGGGCATGG[A/G]GCTTGTCTTGGAGGG	76681
rs238167114	snp	C/T			intron-variant, nc-transcript-variant	Trim12a, Gm15133	Mm_Celera	7:104315096	CAACAAAGTTCTGGA[C/T]CTCGTCGACAAGGTA	76681
rs238253662	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104310459	ATTGATCTAACTATT[A/C]TGACAGGTATAAGAT	76681
rs238386059	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104310338	TTTTGTGAGGAGCAG[A/C]CATATTGATTTCCAT	76681
rs238498825	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104310023	CAATATCCACATATA[A/G]GTGAATATACACCGT	76681
rs238949348	snp	G/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104317034	TTTTTTTTTTTTTTT[G/T]GAGGCAGATATTTAC	76681
rs239002968	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104300930	GTCCTTTTCTTCTGT[A/G]GATAAGGGGAAGAGT	76681
rs239235408	snp	A/T			intron-variant	Trim12a, Gm15133	Mm_Celera	7:104315136	ATTACAGATTGTGAA[A/T]CGGAAGGGGGAGACT	76681
rs239476467	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104312334	ACATCATTTTATCAA[A/T]AGATTATTATCATAC	76681
rs239627063	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104301527	GTGTGGAAAGTATTC[A/C]CATGAATGTTATGTG	76681
rs239818705	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309701	CTGACTACAAAAGAT[A/G]GCCAGTTCAGACTCT	76681
rs239872838	snp	C/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316837	TCAGTGATTGAACCA[C/T]GGTCCTTGTGGATGC	76681
rs240301512	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104305591	CAAGACCAGTATTTA[A/C]CTTACAGATATCTGT	76681
rs240328561	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104312103	tgtatgaagactcta[A/C]tgctgtacctagcta	76681
rs240475639	snp	C/T			intron-variant	Trim12a	Mm_Celera	7:104305969	CTCTTGGGCATCAGG[C/T]TGACACCCTTAGGAA	76681
rs240625932	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104305563	atagttgacctagta[A/C]ttgctatgtacacaa	76681
rs240666781	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104311457	TTTTGCTAGGATGAC[A/G]ATGTTTACTAGTTCA	76681
rs241179360	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104310552	AACTGTTTCTCAGCT[A/T]TTAGAGATTTTTCTA	76681
rs241217626	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309463	TAAGAACCAACACCA[C/T]CAACAAGGTGTCTCT	76681
rs241619986	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104305546	GGTTTTACCTTGTAG[C/T]CATAGTTGACCTAGT	76681
rs241759535	snp	A/C/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313364	ATATGTAAATATAAT[A/C/G]AATAAATAAATCTTA	76681
rs242046833	snp	C/T			intron-variant	Trim12a	Mm_Celera	7:104303282	cttgatgataatgga[C/T]tgagcctctgaattt	76681
rs242109786	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104307470	tctccacctccatga[C/G]attaccgaaccatac	76681
rs242742669	snp	A/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313468	ACAGGACACTCCCAA[A/T]GACAGCGGCATACGC	76681
rs242775444	snp	G/T			intron-variant	Trim12a, Gm15133	Mm_Celera	7:104315205	TGTTGTTGTTGTTGA[G/T]GAGGCACCTCCCTCA	76681
rs242804891	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309095	AGAGCAAGTGTGGTG[A/G]CAAGTGGGTGTCTAC	76681
rs243194721	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104302072	AACTCTTCAATTCCC[A/C]CAACCCATCTCTCTA	76681
rs243371264	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104308027	tttTATTTTGttttg[C/T]tttttgatacagggt	76681
rs243431701	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301970	CTGTTAAATCCAGAT[C/T]CACAGCCACATGCAA	76681
rs243461848	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104305786	TGACCCAGTATCCCT[C/T]CTGACCAAGCATCCT	76681
rs243512804	snp	G/T			intron-variant	Trim12a	Mm_Celera	7:104300660	GGTTATTAATAAAAG[G/T]CTAAGAAGAAAGTGT	76681
rs243550382	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104301398	TCTCAGAACCATGGT[G/T]CTTGCCCTCTAAAAT	76681
rs243762225	snp	C/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104316805	TTTGCTGTTGTTGTT[C/T]AGTTTTGCTTTTGAC	76681
rs244221330	snp	G/T			intron-variant	Trim12a	Mm_Celera	7:104300672	AAGGCTAAGAAGAAA[G/T]TGTACAGGCACTGGA	76681
rs244394466	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301764	CCTACACTCCCATAG[A/G]GTATGGGAAAAAAAA	76681
rs244608598	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309048	AAAGCTGTTGTTCTA[C/T]GTGCTGGGCTGCCTT	76681
rs244641827	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309538	TGAGCTGTGTGGATG[C/T]TGTCTTTGGCAATGG	76681
rs244732007	in-del	-/A			intron-variant	Trim12a	GRCm38.p3	7:104301939	AGACACATCCTATCT[-/A]CCAAAAAAAAAGGAC	76681
rs244918226	snp	A/T			missense	Trim12a	Mm_Celera	7:104300846	CTTACCCTAGTAGCG[A/T]TGAGCCTCTGTGACC	76681
rs245255964	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104311349	TCTTTTTTTTTTCTT[C/T]TTTTTCCATATAAAG	76681
rs245273330	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104312918	GCTTGTCTTGGAGGG[C/T]CATTGATATACCCAG	76681
rs245889198	snp	C/T			intron-variant	Trim12a	Mm_Celera	7:104306592	caagcCATTAAGGTA[C/T]CGCTCCCAACCCTCA	76681
rs245905184	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104310196	TAGGTTGTTTCCAGT[G/T]TCTGGTTATTATAAA	76681
rs246475388	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104308506	catgaaaagacccaa[A/C]ctaagaataatagca	76681
rs247168150	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104308308	AACTGAGGAAATCCT[A/T]AAAATGGCAAACCTG	76681
rs247347851	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309965	CTGTATCTAACCTTT[C/T]TGGGTCTCTGGATTA	76681
rs248109184	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104308130	CTCCGAAGTGCTGGG[A/T]TTAAAGCCATGCACC	76681
rs248236284	snp	A/C			missense	Trim12a	GRCm38.p3	7:104307205	ATTTGATGGATTCAA[A/C]GTACAACGTGATGCA	76681
rs248372073	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309942	TGCTTACCTCCTAGA[A/G]CTCTCCTCTGTATCT	76681
rs248401715	snp	C/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313722	aaatgataatggatg[C/G]acacacctcagcatt	76681
rs248408632	snp	C/T			intron-variant	Trim12a	Mm_Celera	7:104300642	CCTGCAACTCCTCCT[C/T]TTGGTTATTAATAAA	76681
rs248504130	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104301748	GGATACCTATCCTCC[A/T]CCTACACTCCCATAG	76681
rs248509680	snp	A/C/G			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104316407	CATGAGGATCAGGAG[A/C/G]TCAAAGCCATCCTCA	76681
rs248522791	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104312841	AATACCCTAATATAC[C/G]CTACAAAGAAACAAT	76681
rs248542670	snp	A/T			utr-variant-3-prime, missense	Trim12a	Mm_Celera	7:104300304	ACCACTTCTGCCTGG[A/T]TGAAAGATCTCCCCT	76681
rs248638360	snp	A/T			intron-variant	Trim12a, Gm15133	Mm_Celera	7:104315170	TCTGGACAACAGGCA[A/T]CTTTAAAGTAGTTTT	76681
rs248801198	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104310427	CATCTTCACCAACAT[G/T]AGCTGTCACTTTTGT	76681
rs248933810	snp	A/C/T			intron-variant	Trim12a	GRCm38.p3	7:104312745	AAACCAACCAACCAA[A/C/T]CAAACAAACAAACAA	76681
rs249356861	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104301353	TCTCCTTCAAATTAC[A/T]TTCAACGAAGTGTTG	76681
rs249588059	snp	G/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	Mm_Celera	7:104314792	AACTTTCCTAATGCT[G/T]CAACTCTTTAGAAAA	76681
rs249690944	snp	C/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104317010	GTTATGAAAAACCCT[C/T]TACCTTTTTTTTTTT	76681
rs249922715	in-del	-/C			intron-variant	Trim12a	GRCm38.p3	7:104302071	AACTCTTCAATTCCC[-/C]ACAACCCATCTCTCT	76681
rs250070070	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310424	TGACATCTTCACCAA[C/T]ATTAGCTGTCACTTT	76681
rs250176314	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310295	CCAAGAGTGGTATAG[C/T]TGGGCCTTGAGGTAG	76681
rs250369359	snp	A/G			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104317153	CTTGAGTTCAGGGAC[A/G]AGAGGCAGGAGCTAC	76681
rs250683534	snp	C/G			intron-variant	Trim12a	Mm_Celera	7:104302968	ACTTTTCACACATAT[C/G]TCATGGACTTCCCTT	76681
rs250765626	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104305583	TATGTACACAAGACC[A/G]GTATTTAACTTACAG	76681
rs250806868	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104305722	CCATTACCCACCCAT[C/T]CCCAAGTATCTTCTT	76681
rs250881463	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104307559	CCAAGCTGCCCTAAG[C/T]AGCCTGTTAGCCCAG	76681
rs251108662	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104309235	GTGTGCCTATGGCCC[A/T]CCTGTACTTTGGGGA	76681
rs251467796	snp	A/G/T			intron-variant	Trim12a	GRCm38.p3	7:104307685	AAGTATATCCACCAG[A/G/T]GTCATGCCACACCAG	76681
rs251546941	snp	C/G			intron-variant	Trim12a	Mm_Celera	7:104302294	GAAAACAGGAATTAA[C/G]ACTTCTCATTAAGAT	76681
rs251691672	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309769	TATAGATTCCAGAAA[A/G]TTTCCACATCACCCC	76681
rs251738738	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104310322	GTAGATCAATTCCCA[A/G]TTTTGTGAGGAGCAG	76681
rs251784172	snp	A/C			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104317074	AAGCCTGGGCTAGAA[A/C]TCACTAAGTGTTTAG	76681
rs251831089	snp	A/C/G			intron-variant	Trim12a	GRCm38.p3	7:104300975	GGGTCCTTTAAAGAT[A/C/G]AACAGTCATTTCCCA	76681
rs251978967	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104311479	ACTAGTTCATCCTAC[A/G]AATCCCTAAGGATGG	76681
rs252168000	snp	A/G			intron-variant	Trim12a	Mm_Celera	7:104306328	AAGAAGGCAAACAGG[A/G]ACAAAATCAACTTGG	76681
rs252235286	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104308484	acatccaggaaatct[A/G]ggaaaccatgaaaag	76681
rs252603284	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104312127	ctagctagaatcaga[A/G]ccatcgtacctaatt	76681
rs252653123	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309592	AAACCACCCTCTGTC[C/T]TAGCATCAGCTTGGG	76681
rs252768835	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309873	ctacttctatcccta[C/T]cagccccctgtccac	76681
rs253561237	in-del	-/TTTT			intron-variant	Trim12a	GRCm38.p3	7:104310077	CCTCACCCAGGAAGG[-/TTTT]CTTTTTTTCTAACTG	76681
rs253619799	snp	C/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104317129	CTTGGAATACTAATT[C/T]GTCAAACTCTTGAGT	76681
rs253655745	snp	A/G			utr-variant-3-prime, synonymous-codon	Trim12a	Mm_Celera	7:104300292	TGGCTTTTCTTCACC[A/G]CTTCTGCCTGGATGA	76681
rs253701692	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301697	AGTGTCTCAGGAAAA[C/T]CCTGGTTGCCAGCTT	76681
rs253732677	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104302007	AGGGTGAATTACAAT[A/G]GAGTTAAGAGTACCC	76681
rs253740661	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301380	GTTGGGAAGGTCTTA[C/T]ATTCTCAGAACCATG	76681
rs254038854	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104308750	TTTACTGAGAGGCTC[A/C]ACCCAGTAGCTGACC	76681
rs254383731	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104301870	CAACAGAGAAAGATT[C/G]AATGTCTTCTAGCCC	76681
rs254499528	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301638	GAAGAAATTCAAAAC[A/G]GTTGGAAAAGATGAG	76681
rs254611467	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104311309	CAGTTCTTTTATTGT[A/T]TAGCATTGTTTTAGC	76681
rs255360516	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301660	AAAGATGAGGACAAC[A/G]AACTAAGACTAATAT	76681
rs255502366	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310031	ACATATAGGTGAATA[C/T]ACACCGTATTTGTCT	76681
rs255650269	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104310507	CTAATTTGCTTTTTC[C/G]TGATGGCTAAGAATG	76681
rs255988892	snp	A/G			intron-variant	Trim12a	Mm_Celera	7:104302823	aaaaaagagtcaatt[A/G]GAAGTTAGGGCAATA	76681
rs256020178	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309785	TTTCCACATCACCCC[A/G]CAAATGCCCTCTGAT	76681
rs256024929	snp	A/G			intron-variant	Trim12a	Mm_Celera	7:104300721	TCACAGGAGAGGCAG[A/G]ACATTGCAGGAGCAT	76681
rs256055555	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104312703	caccagggctacacg[A/C]agaaaccctgtcttc	76681
rs256287809	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104311346	GGGTCTTTTTTTTTT[C/T]TTTTTTTTCCATATA	76681
rs256419780	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104312906	CCTGGGCATGGGGCT[G/T]GTCTTGGAGGGTCAT	76681
rs256610727	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301771	TCCCATAGGGTATGG[A/G]AAAAAAAAGGATAGT	76681
rs256925726	snp	C/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313044	TAAAAGAATTTAAAA[C/T]GTTTTTAAAAATAAA	76681
rs257341189	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310078	CCTCACCCAGGAAGG[C/T]TTTTTTTCTAACTGC	76681
rs257761197	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301814	CATCAAAAAGCATTA[C/T]GTGCAGAGAGTCAAG	76681
rs258006970	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104309262	GGGAGAAGTGTAGGT[C/G]TTTGGACTTGTGGCA	76681
rs258227024	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104305788	ACCCAGTATCCCTTC[A/T]GACCAAGCATCCTCT	76681
rs258352443	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104308162	CCATTTCCCAGCCAT[A/G]TAGAGGTCTTTTAAA	76681
rs258608741	snp	A/C			nc-transcript-variant, upstream-variant-2KB	Gm15133, Trim12a	Mm_Celera	7:104317645	ATTCTCATTCTTCAA[A/C]CAAAGCATGGCCACG	76681
rs258674311	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104311490	CTACAAATCCCTAAG[C/G]ATGGAAGATCTTTCC	76681
rs258697877	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104307845	cacagcgcacccact[A/G]cagaagaccctggat	76681
rs258708070	snp	A/C			missense	Trim12a	GRCm38.p3	7:104307211	TGGATTCAAAGTACA[A/C]CGTGATGCAGCCTTG	76681
rs258908885	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309483	AAGGTGTCTCTTTGC[C/T]CACTGCCAAGGGTGG	76681
rs259273193	snp	C/T			intron-variant	Trim12a	Mm_Celera	7:104305992	CTTAGGAAGGGTCCC[C/T]ACTTGCCTCCCAGTA	76681
rs259860666	snp	A/G			intron-variant	Trim12a	Mm_Celera	7:104303093	cttttaggaggcttg[A/G]tcttgttggaatacg	76681
rs259984186	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104300939	TTCTGTGGATAAGGG[A/G]AAGAGTTGGAAACCG	76681
rs260082611	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309103	TGTGGTGGCAAGTGG[A/G]TGTCTACAGCACACA	76681
rs260105900	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104301539	TTCACATGAATGTTA[A/T]GTGTGAGAAATATAT	76681
rs260166801	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104312925	TTGGAGGGTCATTGA[C/T]ATACCCAGCAACACA	76681
rs260311007	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104302073	ACTCTTCAATTCCCA[A/C]AACCCATCTCTCTAC	76681
rs260517633	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104308035	TGttttgttttttga[G/T]acagggtttctctgg	76681
rs260800422	snp	C/G			intron-variant	Trim12a	Mm_Celera	7:104300723	ACAGGAGAGGCAGGA[C/G]ATTGCAGGAGCATTA	76681
rs261066672	snp	A/T			intron-variant	Trim12a	Mm_Celera	7:104300893	AATTTACAATATTAA[A/T]TGCATGCAAAGGCAC	76681
rs261701116	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309734	ATCCTCTATTACTGA[A/G]TCCTCACTAGGGTCA	76681
rs262048736	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309498	TCACTGCCAAGGGTG[A/G]TGGTGGGGACTACTC	76681
rs262708359	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104310402	TGAGGGGAATTTTTC[A/T]CTTGCTTGACATCTT	76681
rs263036837	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104312856	GCTACAAAGAAACAA[A/T]CAAACATGGAATCCA	76681
rs263065637	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309066	GCTGGGCTGCCTTGT[C/T]TGACCACAGTGGGAG	76681
rs263097660	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104308311	TGAGGAAATCCTTAA[A/G]ATGGCAAACCTGGGA	76681
rs263344230	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104308551	ccaaggcccagaaag[A/T]actctctcaacaaaa	76681
rs263539383	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104301927	TGCAAACATACAAGA[A/C]ACATCCTATCTACCA	76681
rs263570091	snp	G/T			intron-variant	Trim12a	Mm_Celera	7:104306905	ACCCTCCAACCCCCC[G/T]CCTTACCTTGTACTC	76681
rs263593991	snp	A/G			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104317042	TTTTTTTGGAGGCAG[A/G]TATTTACTCTATATT	76681
rs263707377	snp	A/T			intron-variant	Trim12a	Mm_Celera	7:104300507	CTTGAAATTGAGCAG[A/T]AAAAGTCTTTTTTTT	76681
rs263774598	snp	A/G			intron-variant	Trim12a, Gm15133	Mm_Celera	7:104315138	TACAGATTGTGAATC[A/G]GAAGGGGGAGACTAA	76681
rs263839627	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104305842	CCAGCTCAGGTGTGA[A/T]ACACTGACTCTGCAT	76681
rs264058895	snp	A/T			downstream-variant-500B	Trim12a	Mm_Celera	7:104299757	TTTTTTTTTAATGTG[A/T]TCCCCTGTATTCCTG	76681
rs264118230	snp	G/T			intron-variant	Trim12a	Mm_Celera	7:104302315	TCATTAAGATAAAGG[G/T]GTTGTGGGGGGGAGA	76681
rs264142112	snp	C/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	Mm_Celera	7:104317079	TGGGCTAGAAATCAC[C/T]AAGTGTTTAGAGTGT	76681
rs264161884	snp	C/G			missense	Trim12a	GRCm38.p3	7:104301154	TTCTTTGTTCCCTGG[C/G]GATGGCTTTGGGCTT	76681
rs264337342	snp	A/C			intron-variant, nc-transcript-variant	Trim12a, Gm15133	Mm_Celera	7:104315081	AATGACTGTCATAGA[A/C]AACAAAGTTCTGGAT	76681
rs264820367	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104310005	TATCATTTACTTAAC[A/G]GGCAATATCCACATA	76681
rs265471230	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104309478	CCAACAAGGTGTCTC[G/T]TTGCTCACTGCCAAG	76681
rs265604936	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104309920	ttccccttcccaggg[A/T]tatacatgcttacct	76681
rs265670379	snp	C/T			intron-variant	Trim12a	Mm_Celera	7:104303003	GCCGTACATTTTTTT[C/T]TCTCTCTCTCATTAT	76681
rs265839418	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104308150	AGCCATGCACCACCA[C/T]TTCCCAGCCATATAG	76681
rs265932239	snp	A/G			intron-variant	Trim12a	Mm_Celera	7:104300645	GCAACTCCTCCTCTT[A/G]GTTATTAATAAAAGG	76681
rs265988952	snp	C/G			downstream-variant-500B	Trim12a	Mm_Celera	7:104299630	CTGGGAGGGAATGGG[C/G]ATGGAGACACTTGAG	76681
rs266086249	snp	G/T			intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104315188	TTAAAGTAGTTTTTT[G/T]TTGTTGTTGTTGTTG	76681
rs266149777	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310596	GTTTAGATCTGTGCC[C/T]GTCTTTAATTGGATT	76681
rs578337194	snp	C/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313134	CAAGAACAAAGATGA[C/T]GATTTATGGGGCATT	76681
rs578429284	snp	A/G			upstream-variant-2KB, nc-transcript-variant	Trim12a, Gm15133	GRCm38.p3	7:104317376	GTGAAAAGGATGAAG[A/G]TGACCAGGTGAGCAA	76681
rs578487434	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104301242	CAGTGACCCCCAACT[A/C]CCACAGATTCCTCTC	76681
rs578514007	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104308524	AAGAATAATAGCAAG[A/T]GAGTTCCAGCTCCAA	76681
rs578541329	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104305870	CATCTCCAACCAGGG[G/T]AACCAGTAGGGAGGA	76681
rs578550520	snp	A/T			missense	Trim12a	GRCm38.p3	7:104307172	GGCACACAGGGCAAA[A/T]GAACACTTTCTTATC	76681
rs578564014	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104302729	AAGAGAAAGATTTGT[G/T]GGAATGAGTCAGAAA	76681
rs578597531	snp	A/G			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104316101	TGACCACCACAGTGG[A/G]GAGCCTGATAACAGG	76681
rs578636135	snp	A/G			downstream-variant-500B	Trim12a	GRCm38.p3	7:104299494	GGGGCAGGGGGAAGG[A/G]GAAAGGGCTCAGAGA	76681
rs578637784	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104313030	GGGGAAAAATATAAT[A/G]AAAGAATTTAAAACG	76681
rs578899438	snp	A/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314878	ACTATATTTTTCTAC[A/T]GTTTTGAATCATAAT	76681
rs578941090	snp	G/T			upstream-variant-2KB, nc-transcript-variant	Trim12a, Gm15133	GRCm38.p3	7:104317314	TCCACTCTCAACTCT[G/T]CAAAGATTAGACTTT	76681
rs578948090	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104311270	TATAATACAACTTGA[A/T]ATCAGAGATGGTGAT	76681
rs578948694	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104308986	TGTAGCAGATGTGCA[A/G]CTTGACCTTCATGTG	76681
rs578953787	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104301493	TTAAAACAAACCATA[A/T]CTAATGCCTGAAAAA	76681
rs578962693	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104305674	ACATTCTGCTTTTAA[C/T]TCCCTGGCAGAAGTT	76681
rs578996417	snp	A/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313191	GAGTGTTCCACAAGA[A/T]GATGAAGCAGGGGCT	76681
rs578999642	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104307394	CTCAGGTGCCTATGT[G/T]ATTGGGATGGTGAAA	76681
rs579007041	snp	A/T			downstream-variant-500B	Trim12a	GRCm38.p3	7:104299625	CTAACCTGGGAGGGA[A/T]TGGGCATGGAGACAC	76681
rs579054612	snp	A/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104315896	CTGGGAATGAGGTTC[A/T]GTTGACATAGTGCTT	76681
rs579089505	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104310250	TGCAAATGTCCTTGT[A/G]GTATGGTGGAGCTTC	76681
rs579110714	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104302672	AGTTTATTGAGGCAG[A/C]AAACAATGACATCTA	76681
rs579124130	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301405	ACCATGGTGCTTGCC[C/T]TCTAAAATTAAACAG	76681
rs579167228	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104306315	AGAAACTTTTGAAAA[C/G]AAGGCAAACAGGAAC	76681
rs579178889	snp	A/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314676	GCTGAAGTTATTCCC[A/G]GGCTTGGGACTGTCA	76681
rs579185164	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104308780	CCAGATAGGTACAGA[C/G]ACCCACAGCCAAACA	76681
rs579200474	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104311556	TGAAGTTTTTATCAT[A/T]CAAGTCTTTCACTTA	76681
rs579223484	snp	G/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314881	ATATTTTTCTACAGT[G/T]TTGAATCATAATATG	76681
rs579464631	snp	A/G/T			intron-variant	Trim12a	GRCm38.p3	7:104304450	GCGTGTGAATTGTTG[A/G/T]TTTTGTTTTGTTTTT	76681
rs579517552	snp	A/C			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313883	ATACTTGGCCTCAGG[A/C]AAGTAGACAAAAAAT	76681
rs579529701	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104300767	AAGCAACATGAGGCC[A/T]AACAGAAACATAAGC	76681
rs579572063	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104308054	GGGTTTCTCTGGATA[A/G]CCCTGCCTGTAATGG	76681
rs579575555	snp	A/G			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104316239	GAATCTTGAAAGCTT[A/G]CACCCATGCCATACC	76681
rs579578588	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310648	ATTGGATTTGGGTTT[C/T]TGATATCTAATCTTT	76681
rs579590302	snp	A/G			synonymous-codon	Trim12a	GRCm38.p3	7:104306954	GAGAGCTGTTTTGTG[A/G]CCACGGTGCTCCTGA	76681
rs579594768	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104309374	GTTTAAAACCACTTT[G/T]GCCACCAAGCCAGGT	76681
rs579613385	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301931	AACATACAAGACACA[C/T]CCTATCTACCAAAAA	76681
rs579707305	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104307931	GATAGAGGCCTTTAA[A/G]GAGGAAATGGATAAA	76681
rs579726264	snp	G/T			utr-variant-3-prime	Trim12a	GRCm38.p3	7:104300026	ACCCACCTGATGTAA[G/T]TGACAGCCCTTAGCT	76681
rs579736302	snp	A/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313604	ATGAAATTAGAAATC[A/G]CCAAAAGAGAGATTT	76681
rs580029301	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104302573	GGGGCGGGGAGGTGA[G/T]AATCCTCACAACTGA	76681
rs580038711	snp	A/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104316727	ACTCTTCTTCCTTTC[A/T]GATAGCCTGACCCTA	76681
rs580041722	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310954	AGGTGTCCATAGGTG[C/T]GTGAATATATGTCTG	76681
rs580048113	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104305221	TGAGCTACCATGTGG[A/T]TGTAGGGAACCAAAT	76681
rs580067158	snp	A/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104315021	ATCACACAAAAACGC[A/T]GTAAAAAGCAGAGGC	76681
rs580106581	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310683	TTCTTTATTAAACCT[C/T]TATCAGATATGGTGT	76681
rs580109729	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309854	TCCCCTAACCTGATC[C/T]GTCCTACTTCTATCC	76681
rs580138999	snp	G/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104316348	GGCTTTGGGGCCATT[G/T]TTATTCAAACCGGCA	76681
rs580153122	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104304952	ATCTGATGTCCTCTT[C/G]TGACTTCCATGGGAA	76681
rs580211622	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104311749	CATACGTAGCTACTA[A/C]ATTCCTTCTCCTTGG	76681
rs580215891	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104306613	CCAACCCTCATCTTA[C/T]TTACTTTGACACCTA	76681
rs580311095	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104302268	TTCTCCACACCCTAG[A/G]TAGAAACAGAGAAAA	76681
rs580573688	snp	C/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314958	TCATTCAAACGGGTC[C/T]GATCCGGTAAAGAAC	76681
rs580581821	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104309806	GCCCTCTGATTCAAC[G/T]GTCTCTCCCTGCATT	76681
rs580633450	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104305412	TCTACCCATCCATCT[A/T]TCCTTCCTTCCTTCC	76681
rs580668254	snp	A/T			downstream-variant-500B	Trim12a	GRCm38.p3	7:104299509	AGAAAGGGCTCAGAG[A/T]GAACAAGGAGGGGCC	76681
rs580688429	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104310972	GAATATATGTCTGCA[A/T]CTTCAATTCAGTTCC	76681
rs580695119	snp	C/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314554	TCTTATTGAGTTGCT[C/G]ATGATGGCCATCAAT	76681
rs580701249	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104308531	ATAGCAAGAGAGTTC[A/C]AGCTCCAAGGCCCAG	76681
rs580701801	snp	A/C/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313091	TACCATCACTCTTAC[A/C/T]GTGTCATGTCAAAGA	76681
rs580745028	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104310123	AAATTTCATGATGCC[A/G]TTTTTAAAACACGCA	76681
rs580772610	snp	C/T			synonymous-codon	Trim12a	GRCm38.p3	7:104307296	GACAGGACAGGTCAC[C/T]TCCTCCTTTAAATTC	76681
rs580783331	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104301315	AGAGGTAGAGAGATG[C/G]CAGTCACATGAATAC	76681
rs580824540	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104302633	CACAAGGAGCTGATT[A/C]CTGCAAGGGATAGTC	76681
rs580885636	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104310137	CATTTTTAAAACACG[A/C]AAGTAATACCAGATT	76681
rs581038173	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104308522	CTAAGAATAATAGCA[A/T]GAGAGTTCCAGCTCC	76681
rs581093296	snp	A/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314313	CTGTCGGAAGAGCTG[A/G]AGACCAGTCTGGGCA	76681
rs581205353	snp	A/G			upstream-variant-2KB, nc-transcript-variant	Trim12a, Gm15133	GRCm38.p3	7:104317320	CTCAACTCTGCAAAG[A/G]TTAGACTTTACATTT	76681
rs581211808	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104311299	ATACTTCCAGCAGTT[C/T]TTTTATTGTATAGCA	76681
rs581246973	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104312970	TGATTTTTAAATTTT[A/C]AGAGAGTAGGCATGA	76681
rs581279747	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104311168	TCGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC	76681
rs581326916	snp	C/T			missense	Trim12a	GRCm38.p3	7:104307096	TTGAACATTTTGAGC[C/T]TCTCTACTATGTTGG	76681
rs581358240	snp	C/G			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104317242	GTCTGGGAATTAAAA[C/G]TATTAAATACCCAGA	76681
rs581360120	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104308390	ATGGAAGAAAGAAAC[C/T]CAGATGTAGAAGATA	76681
rs581366451	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104305522	CTACCTACGTACCTA[C/T]CTAGACCCGGTTTTA	76681
rs581419756	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301083	CAATCACGGAGCATA[A/G]CTCTCCTCACCTTGC	76681
rs581421580	snp	A/C			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314285	CTGACACTACAGAGA[A/C]TTGGAAGTGGGGCTG	76681
rs581663283	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104305935	AAGTAAAGACCCCAG[A/G]AGCTTCTTGCCAAGG	76681
rs581691507	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104312610	GTGGTGCACACCTTT[A/C]ATCCCAGCACTTGGG	76681
rs581758426	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104311519	CCATCTTGTGATACC[C/T]TTTTCAGATTCTTCA	76681
rs581761600	snp	G/T			missense	Trim12a	GRCm38.p3	7:104307072	TTCTGCTCCTCTTCT[G/T]GGCTGGGCTTGAACA	76681
rs581782176	snp	A/G			upstream-variant-2KB, intron-variant, utr-variant-5-prime	Trim12a, Gm15133	GRCm38.p3	7:104315797	CACCAGAATGTCTTG[A/G]AGGTTCCTATTTGGC	76681
rs581813781	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309434	ACTGCCATCTGCTCT[A/G]CCCCTGACTGATGTA	76681
rs581875612	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104302187	GGAGAAATTATGTTC[C/G]CCTTGAAAACTAAAT	76681
rs581877544	snp	A/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314945	TCCCGTGAAAAGGTC[A/G]TTCAAACGGGTCTGA	76681
rs581987854	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104302735	AAGATTTGTGGGAAT[A/G]AGTCAGAAATAAGAT	76681
rs581996815	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104310619	ATTGGATTATACTTT[A/T]AATTATATTGTTAAT	76681
rs582191369	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104309023	GAACAACTGGAATGG[A/G]GGCTATCTAAAAGCT	76681
rs582216181	snp	A/G			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104316071	GCACTCACAGTTCCT[A/G]TGGGTTAGAGTTCAT	76681
rs582217513	snp	C/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104316127	ACAGGCAGGGAGACA[C/T]GGTGCTGGAGCAGAA	76681
rs582246305	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104302689	AACAATGACATCTAA[C/T]TGAGGGGCAGACAAA	76681
rs582276509	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301751	TACCTATCCTCCTCC[C/T]ACACTCCCATAGGGT	76681
rs582340204	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104305863	GACTCTGCATCTCCA[A/G]CCAGGGTAACCAGTA	76681
rs582366972	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301407	CATGGTGCTTGCCCT[C/T]TAAAATTAAACAGTT	76681
rs582400850	snp	A/G			downstream-variant-500B	Trim12a	GRCm38.p3	7:104299631	TGGGAGGGAATGGGC[A/G]TGGAGACACTTGAGA	76681
rs582429084	snp	C/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313242	AAGAGCACCCGACTG[C/T]TCTTCCGAAGGTCCG	76681
rs582434846	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104307901	AAATGAATCTAAATT[C/G]AATCTTATAAAGATG	76681
rs582593018	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104311660	TTTTCAGTTCACTTG[C/T]CATTTATATAGAGCT	76681
rs582606087	snp	G/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314701	CTGTCAAACAGGGTC[G/T]ATGACTAAATAACAG	76681
rs582610242	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104308941	ACTAAAGAATATACA[A/C]TGGCTGGGACCTATG	76681
rs582644956	snp	C/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314934	TAAAGTGAAACTCCC[C/G]TGAAAAGGTCATTCA	76681
rs582750379	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310655	TTGGGTTTTTGATAT[C/T]TAATCTTTTGAGTTC	76681
rs582829253	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104306395	AGAATCTAGGAGTAG[A/G]AAGAAAATAATAAGG	76681
rs582836785	snp	A/C			synonymous-codon	Trim12a	GRCm38.p3	7:104306957	AGCTGTTTTGTGACC[A/C]CGGTGCTCCTGAGAT	76681
rs582898956	snp	C/G			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104316334	TTCAAAAGATCTTAG[C/G]CTTTGGGGCCATTGT	76681
rs582913119	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104304502	TTCCAGACAGGGTTT[C/T]TCTGTGTAGCCCTGC	76681
rs582991677	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104312351	GATTATTATCATACT[C/G]TAGTAACTGACTCCA	76681
rs583000811	snp	A/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313135	AAGAACAAAGATGAT[A/G]ATTTATGGGGCATTA	76681
rs583006682	snp	A/T			utr-variant-5-prime	Trim12a	GRCm38.p3	7:104307348	GTTGCTGTGATCCTG[A/T]GTATGACTGTCCTGA	76681
rs583008906	snp	C/T			downstream-variant-500B	Trim12a	GRCm38.p3	7:104299608	AAAGGAATGTAAATG[C/T]GCTAACCTGGGAGGG	76681
rs583146163	snp	A/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313618	CACCAAAAGAGAGAT[A/T]TGGAAAAAATTTCAC	76681
rs583165669	snp	A/G			utr-variant-3-prime	Trim12a	GRCm38.p3	7:104300032	CTGATGTAAGTGACA[A/G]CCCTTAGCTATGGCC	76681
rs583324208	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104307976	ACAGGAACATACAAT[C/T]AGAGGTGGTTTTTCG	76681
rs583367011	snp	C/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104316957	ACAATTGCTTACAAA[C/T]AATGCTTTGATGTTC	76681
rs583373161	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310970	GTGAATATATGTCTG[C/T]ATCTTCAATTCAGTT	76681
rs583379484	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104305243	GAACCAAATTCAAGT[C/T]CTCTGCAAGAGCAAG	76681
rs583389430	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104308405	TCAGATGTAGAAGAT[A/T]CAAGAGAAGAAATTG	76681
rs583400703	snp	G/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104315022	TCACACAAAAACGCA[G/T]TAAAAAGCAGAGGCT	76681
rs583488906	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104302629	AATACACAAGGAGCT[A/G]ATTACTGCAAGGGAT	76681
rs583536450	snp	A/G			missense	Trim12a	GRCm38.p3	7:104301126	ATGCCTTGCAGGTCA[A/G]GGGCTCGGAACTTTC	76681
rs583553056	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104312199	GAATCTACCTTGAAA[A/T]GTTTAAAGGAGATAG	76681
rs583561022	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104306696	CTGTAAAAACACTTG[C/T]TCTTGTTCTAGAGTT	76681
rs583588631	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104310718	AAAATCTTTTCCCAT[G/T]TTTTGTCCAATTGGT	76681
rs583657242	snp	A/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314290	ACTACAGAGACTTGG[A/G]AGTGGGGCTGTCGGA	76681
rs583660798	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104305203	TAGAATTATGGATAG[A/T]TATGAGCTACCATGT	76681
rs583734078	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104302285	AGAAACAGAGAAAAC[A/C]GGAATTAACACTTCT	76681
rs583900089	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104309808	CCTCTGATTCAACTG[A/T]CTCTCCCTGCATTCT	76681
rs583989381	snp	A/T			missense	Trim12a	GRCm38.p3	7:104307087	GGGCTGGGCTTGAAC[A/T]TTTTGAGCCTCTCTA	76681
rs583993713	snp	A/C			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314963	CAAACGGGTCTGATC[A/C]GGTAAAGAACCACAG	76681
rs584051647	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104312654	TGGATTTCTGAGTTC[C/G]AGGCCAGCCTGGTCT	76681
rs584131049	snp	A/G			downstream-variant-500B	Trim12a	GRCm38.p3	7:104299560	AGCCAGACCTACCTG[A/G]CTGTTGCTAGGTTAA	76681
rs584141544	snp	A/C			missense	Trim12a	GRCm38.p3	7:104307311	CTCCTCCTTTAAATT[A/C]TTCATGAATTGTGAA	76681
rs584154092	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104300768	AGCAACATGAGGCCT[A/G]ACAGAAACATAAGCT	76681
rs584168914	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104308267	CAAGACCTGAAAGTC[A/G]AAATGGAAGCAATAA	76681
rs584212031	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104302651	GCAAGGGATAGTCTG[A/T]AAATGAGTTTATTGA	76681
rs584231267	snp	C/G			intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104315261	AGAGGCCGGCAGCCC[C/G]TCCCCCTTTCCCTCC	76681
rs584236897	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310147	ACACGCAAGTAATAC[C/T]AGATTGTATGAATGT	76681
rs584313077	snp	G/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314320	AAGAGCTGAAGACCA[G/T]TCTGGGCAACATAAA	76681
rs584321201	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301229	CTGCAATCCCTCCCA[A/G]TGACCCCCAACTCCC	76681
rs584347083	snp	A/C			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313106	AGTGTCATGTCAAAG[A/C]CAGAGGTCATGACAA	76681
rs584535990	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104308523	TAAGAATAATAGCAA[G/T]AGAGTTCCAGCTCCA	76681
rs584614683	snp	A/G			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104316079	AGTTCCTATGGGTTA[A/G]AGTTCATGACCACCA	76681
rs584618089	snp	C/T			upstream-variant-2KB, nc-transcript-variant	Trim12a, Gm15133	GRCm38.p3	7:104317343	TTACATTTAGTCTGC[C/T]ATTACCCTCTGACCT	76681
rs584625993	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104311365	TTTTTCCATATAAAG[A/T]TGAAAATTGTCCTTT	76681
rs584634539	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104305869	GCATCTCCAACCAGG[G/T]TAACCAGTAGGGAGG	76681
rs584660120	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104312985	AAGAGAGTAGGCATG[A/G]AATTGGGTGAGTAAT	76681
rs584667743	snp	A/C			missense	Trim12a	GRCm38.p3	7:104307171	CGGCACACAGGGCAA[A/C]TGAACACTTTCTTAT	76681
rs584692407	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104308955	ACTGGCTGGGACCTA[C/T]GCCTCCTCGCTCATA	76681
rs584697394	snp	A/G			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104317262	AAATACCCAGACTAT[A/G]ATCTAACTCTGCATG	76681
rs584709854	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104302714	GACAAAGTGATGAAT[A/C]AGAGAAAGATTTGTG	76681
rs584814405	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104302665	GAAAATGAGTTTATT[A/G]AGGCAGAAAACAATG	76681
rs584837249	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104311189	CCTCTGCCTCCCAAG[G/T]GCTGAGACTAACGGC	76681
rs584844155	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104305541	GACCCGGTTTTACCT[A/T]GTAGCCATAGTTGAC	76681
rs584855676	snp	C/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104315894	AGCTGGGAATGAGGT[C/T]CTGTTGACATAGTGC	76681
rs584895680	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104311087	TTTTTTTGGTTTTTC[A/G]AGACAGGGTTTCTCT	76681
rs584911590	snp	C/T			intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104315270	CAGCCCGTCCCCCTT[C/T]CCCTCCCCCGCTTTT	76681
rs584931312	snp	A/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314855	ACTGTGGTCTTTGCT[A/T]CCTCTTAACTATATT	76681
rs585130199	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310192	CAACTAGGTTGTTTC[C/T]AGTGTCTGGTTATTA	76681
rs585168433	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104305416	CCCATCCATCTTTCC[A/T]TCCTTCCTTCCTTCC	76681
rs585215936	snp	A/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314650	GAAAATATCTGAAGG[A/G]GAAGGAAATAGCTGA	76681
rs585219990	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104308754	CTGAGAGGCTCAACC[C/T]AGTAGCTGACCCAGA	76681
rs585224722	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104308016	TTGTTTGTTTGTTTT[A/G]TTTTGTTTTGTTTTT	76681
rs585271473	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104311381	TGAAAATTGTCCTTT[C/G]AAAGCCTGTAAAGAA	76681
rs585275730	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104301330	CCAGTCACATGAATA[C/T]AATCATGTCTCCTTC	76681
rs585314586	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104306713	CTTGTTCTAGAGTTT[A/G]TCGCCCCTGGTAGAT	76681
rs585321922	snp	A/C			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314926	GAGATATCTAAAGTG[A/C]AACTCCCGTGAAAAG	76681
rs585421049	snp	A/C			utr-variant-3-prime	Trim12a	GRCm38.p3	7:104300012	TTAACATGGTCTTTA[A/C]CCACCTGATGTAAGT	76681
rs585473966	snp	A/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313407	AGAAGATGAAGCAGA[A/G]AAGAAAGCAGAGAGG	76681
rs585576615	snp	C/T			utr-variant-3-prime	Trim12a	GRCm38.p3	7:104300148	AGAGTTTTGCCAGTA[C/T]TTAGGACTCAAAAGT	76681
rs585587011	snp	A/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313823	AGAGGGAAGCCTGCC[A/G]GGACTACATTACACA	76681
rs585651812	snp	G/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104316205	AGAGAGAGAATGGTG[G/T]TGGTGGTCAGAATCT	76681
rs585659987	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104310636	ATTATATTGTTAATT[G/T]GATTTGGGTTTTTGA	76681
rs585661470	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104312205	ACCTTGAAAAGTTTA[A/G]AGGAGATAGTTGTTC	76681
rs585689714	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104302745	GGAATGAGTCAGAAA[C/T]AAGATATGCCTAACT	76681
rs585705532	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309063	TGTGCTGGGCTGCCT[C/T]GTCTGACCACAGTGG	76681
rs585802931	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104307910	TAAATTGAATCTTAT[A/G]AAGATGATAGAGGCC	76681
rs585813731	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104301916	TGAACATATATTGCA[A/G]ACATACAAGACACAT	76681
rs585864569	snp	C/T			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104316337	AAAAGATCTTAGGCT[C/T]TGGGGCCATTGTTAT	76681
rs585947588	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104304511	GGGTTTCTCTGTGTA[G/T]CCCTGCCTGTCCTGG	76681
rs586040639	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104311527	TGATACCCTTTTCAG[A/T]TTCTTCAAAGACTTG	76681
rs586149447	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104301491	TCTTAAAACAAACCA[A/T]ATCTAATGCCTGAAA	76681
rs586178784	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104306412	AGAAAATAATAAGGA[A/C]TAAATATCTACTCAG	76681
rs586213803	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310660	TTTTTGATATCTAAT[C/T]TTTTGAGTTCTTTAT	76681
rs586273965	snp	C/T			downstream-variant-500B	Trim12a	GRCm38.p3	7:104299606	TAAAAGGAATGTAAA[C/T]GTGCTAACCTGGGAG	76681
rs586321537	snp	C/T			downstream-variant-500B	Trim12a	GRCm38.p3	7:104299610	AGGAATGTAAATGTG[C/T]TAACCTGGGAGGGAA	76681
rs586343927	snp	A/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313174	ATCAGTATACTTCTT[A/G]TGAGTGTTCCACAAG	76681
rs586350407	snp	C/T			utr-variant-5-prime	Trim12a	GRCm38.p3	7:104307369	ACTGTCCTGACTCCT[C/T]GCACTTCTGCTCAGG	76681
rs586409398	snp	C/T			missense, intron-variant	Trim12a	GRCm38.p3	7:104306010	TTGCCTCCCAGTAAG[C/T]TCTATCCTTCTGAAG	76681
rs586417699	snp	A/C			intron-variant, nc-transcript-variant	Trim12a, Gm15133	GRCm38.p3	7:104315038	TAAAAAGCAGAGGCT[A/C]TGATCCAGCTTTGCT	76681
rs586464086	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104302188	GAGAAATTATGTTCG[A/C]CTTGAAAACTAAATC	76681
rs586505809	snp	C/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314952	AAAAGGTCATTCAAA[C/T]GGGTCTGATCCGGTA	76681
rs586510248	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309805	TGCCCTCTGATTCAA[C/T]TGTCTCTCCCTGCAT	76681
rs586579482	snp	C/T			missense	Trim12a	GRCm38.p3	7:104301130	CTTGCAGGTCAGGGG[C/T]TCGGAACTTTCTTTG	76681
rs586601187	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104310148	CACGCAAGTAATACC[A/G]GATTGTATGAATGTG	76681
rs586614677	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104302654	AGGGATAGTCTGAAA[A/G]TGAGTTTATTGAGGC	76681
rs586762203	snp	A/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314487	GATTGAAAAGTACCC[A/T]ATCACTGAACTAAGT	76681
rs586774262	snp	A/G			intron-variant	Trim12a	GRCm38.p3	7:104310971	TGAATATATGTCTGC[A/G]TCTTCAATTCAGTTC	76681
rs586779933	snp	A/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104314291	CTACAGAGACTTGGA[A/G]GTGGGGCTGTCGGAA	76681
rs586786755	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104305386	TCTTTCTCTATCTAT[C/T]TATCTATCTATCTAC	76681
rs586802329	snp	C/G			intron-variant	Trim12a	GRCm38.p3	7:104310136	CCATTTTTAAAACAC[C/G]CAAGTAATACCAGAT	76681
rs586842544	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104302630	ATACACAAGGAGCTG[A/T]TTACTGCAAGGGATA	76681
rs586953322	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104309829	CCTGCATTCTCTTCC[C/T]CCATCCCTTTCCCCT	76681
rs586965432	snp	A/C			intron-variant	Trim12a	GRCm38.p3	7:104305418	CATCCATCTTTCCTT[A/C]CTTCCTTCCTTCCTT	76681
rs586972712	snp	C/G			upstream-variant-2KB, intron-variant	Trim12a, Gm15133	GRCm38.p3	7:104316680	ATAACTCTGTAGTTT[C/G]AATTTATTTCACATA	76681
rs586978807	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310738	GTCCAATTGGTGGTG[C/T]CCTCTGCCTAACAGA	76681
rs586986190	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104305209	TATGGATAGTTATGA[G/T]CTACCATGTGGATGT	76681
rs587146695	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104312599	GCTGGCCGGTGGTGG[C/T]GCACACCTTTCATCC	76681
rs587198179	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104308503	AACCATGAAAAGACC[C/T]AAACTAAGAATAATA	76681
rs587345531	snp	A/G			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104315019	TTATCACACAAAAAC[A/G]CAGTAAAAAGCAGAG	76681
rs587352996	snp	G/T			intron-variant	Trim12a	GRCm38.p3	7:104302291	AGAGAAAACAGGAAT[G/T]AACACTTCTCATTAA	76681
rs587357986	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104311147	ACTTTGTAGATCAGG[C/T]TGGCCTCGAACTCAG	76681
rs587434920	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104312863	AGAAACAATCAAACA[C/T]GGAATCCATTTGTGT	76681
rs587438234	snp	C/T			missense	Trim12a	GRCm38.p3	7:104307088	GGCTGGGCTTGAACA[C/T]TTTGAGCCTCTCTAC	76681
rs587461252	snp	G/T			intron-variant, upstream-variant-2KB	Trim12a, Gm15133	GRCm38.p3	7:104313953	TGAGAAAGACCCAAG[G/T]AAAATGTAATGAACA	76681
rs587465885	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104308355	CAACAGATGCAAGCA[C/T]CACCAACAGAATACA	76681
rs587484306	snp	A/T			intron-variant	Trim12a	GRCm38.p3	7:104300778	GGCCTAACAGAAACA[A/T]AAGCTCTGCAAGACA	76681
rs587499004	snp	C/T			synonymous-codon	Trim12a	GRCm38.p3	7:104307071	TTTCTGCTCCTCTTC[C/T]GGGCTGGGCTTGAAC	76681
rs864256058	snp	C/T			intron-variant	Trim12a	GRCm38.p3	7:104310641	ATTGTTAATTGGATT[C/T]GGGTTTTTGATATCT	76681
rs864275013	snp	C/T			missense	Trim12a	GRCm38.p3	7:104302245	CCCATACATACCGTT[C/T]TATGATGTTCTCCAC	76681
rs864281626	snp	C/T			downstream-variant-500B	Trim12a	GRCm38.p3	7:104299735	AAATTAAACAAAGGA[C/T]TGTGCTTTTTTTTTT	76681
rs864283882	snp	A/C/T			utr-variant-3-prime, missense	Trim12a	GRCm38.p3	7:104300346	GGTGAGGGTCCAAAG[A/C/T]TGTGTGCGAAAATTT	76681
rs864285125	in-del	-/TA			intron-variant	Trim12a	GRCm38.p3	7:104310223	TAAATAAAGCTGCAC[-/TA]TACATAGTTGTGCAA	76681
rs864297369	in-del	-/T			intron-variant	Trim12a	GRCm38.p3	7:104308026	TTTTATTTTGTTTTG[-/T]TTTTTTGATACAGGG	76681
rs864305283	snp	C/T			synonymous-codon	Trim12a	GRCm38.p3	7:104304159	CTGCAGCCTTACCTG[C/T]AGTATTTCTATGTCT	76681