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

Usp19

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs13475028	snp	C/T	0.375	0.216506	upstream-variant-2KB, missense	Usp19, Lamb2	GRCm38.p3	9:108489547	GCTCAGGGTGCCATC[C/T]GGGGAGCAGTGGTTG	71472
rs13475029	snp	C/T			upstream-variant-2KB, synonymous-codon	Usp19, Lamb2	Mm_Celera	9:108489255	CGAGCAGATCCAGCG[C/T]CTAGCCAGTGAGATT	71472
rs30166363	snp	G/T	0.5	0	intron-variant	Usp19	GRCm38.p3	9:108493980	TCTGTTTTTTTTTTT[G/T]TTTTGTGTGTGTGTG	71472
rs33640744	snp	C/T	0.375	0.216506	intron-variant	Usp19	Mm_Celera	9:108500600	GTTCTGATGTGTATT[C/T]GAGATATTCCCTATC	71472
rs45841050	snp	A/G	0.197531	0.244432	intron-variant	Usp19	GRCm38.p3	9:108491542	TCACTTTGGATGGAG[A/G]GAGCCCGAATCCACA	71472
rs45859985	snp	G/T	0.197531	0.244432	intron-variant	Usp19	GRCm38.p3	9:108493941	AGAGAGGGTACCACT[G/T]GCCGGACCAGAGCTA	71472
rs46040097	snp	C/T	0.18	0.24	intron-variant	Usp19	GRCm38.p3	9:108496025	TGAGTGTCCTGTGAG[C/T]GGATAGTTAAGATTT	71472
rs46156673	snp	A/G	0.32	0.24	synonymous-codon	Usp19	GRCm38.p3	9:108496379	CCTGTTTCAGGGCCA[A/G]TACAAGTCAAAGCTG	71472
rs46338515	snp	A/G	0.35503	0.226867	intron-variant	Usp19	GRCm38.p3	9:108500984	GATTGAAGGCTGTCT[A/G]CAGGAGGTCAAGACT	71472
rs47400315	snp	C/T	0.197531	0.244432	intron-variant	Usp19	GRCm38.p3	9:108492098	TCTCTACTTGTCTGG[C/T]GGTGACTAAGCAGCC	71472
rs47459327	snp	C/T	0.18	0.24	intron-variant	Usp19	GRCm38.p3	9:108493487	CCCTCTCTCCTGGTA[C/T]GTTCCAGTTGCGTGT	71472
rs48307923	snp	C/T	0.124444	0.216185	intron-variant, downstream-variant-500B	Usp19	Mm_Celera	9:108501719	GTCTCTCTGTCTAAA[C/T]GCCGCTGCTGTCTGC	71472
rs48760352	snp	A/G	0.124444	0.216185	intron-variant	Usp19	Mm_Celera	9:108499751	TCCTGTTCGGTGAGC[A/G]ATGAGTGAGGCCTGC	71472
rs48923636	snp	C/T	0.231111	0.249285	intron-variant	Usp19	GRCm38.p3	9:108497828	CAGGACTAAGCCCTC[C/T]GTGGTGCCGTGAAGC	71472
rs49493566	snp	A/C	0.197531	0.244432	synonymous-codon	Usp19	GRCm38.p3	9:108493188	GATTGTTAAGCTGCG[A/C]GTGGGAACAGGTCCC	71472
rs49981711	snp	C/G	0.231111	0.249285	utr-variant-3-prime, intron-variant, downstream-variant-500B	Usp19	GRCm38.p3	9:108502173	TGCCTTCAGTGCTGC[C/G]TGTTTGGTTCTCAGT	71472
rs50320341	snp	C/T			synonymous-codon	Usp19	Mm_Celera	9:108495911	GGCCCTATGGAAGGG[C/T]ACTCACCAAGCCTTT	71472
rs50460722	snp	C/T	0.165289	0.235211	upstream-variant-2KB, intron-variant	Usp19, Lamb2	Mm_Celera	9:108489138	GTCATGCAGGAGAGA[C/T]TGTTAAGCCCTTGCC	71472
rs50614059	snp	C/T	0.244898	0.249948	synonymous-codon	Usp19	GRCm38.p3	9:108498828	CCTTCTGAGCTCCAG[C/T]TGGTGACCCCTGTGG	71472
rs50922789	snp	G/T	0.244898	0.249948	intron-variant	Usp19	GRCm38.p3	9:108500681	TGTCCCTACTGAAAC[G/T]TCAGGCTCTTCTGTG	71472
rs51201795	snp	C/T	0.197531	0.244432	upstream-variant-2KB, intron-variant	Usp19, Lamb2	GRCm38.p3	9:108488942	GTACTTGAGTCTCGG[C/T]GTCTGCAATGGACAT	71472
rs212027787	snp	C/G			intron-variant, downstream-variant-500B	Usp19, Lamb2	GRCm38.p3	9:108490998	GGGCCGTGCCAGCCC[C/G]GACATCTCGAGCCTC	71472
rs212567353	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108492261	TCCAGCGTTGTGGGT[C/T]TCTGTAGATACCCAG	71472
rs212659025	snp	C/G			intron-variant	Usp19	Mm_Celera	9:108494284	AGATTGGGTTGCAGG[C/G]TTGGTGGGTGGGCAT	71472
rs213512879	snp	C/G			intron-variant	Usp19	GRCm38.p3	9:108500633	AGATGGCTGCTGCCT[C/G]GATTGGCTGTCACAC	71472
rs213634771	snp	G/T			intron-variant	Usp19	Mm_Celera	9:108499079	GGTGAGCACTGATGA[G/T]TGTGCTTTGTCTTAG	71472
rs213702387	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108491066	ATGCTACCCCTGTGG[C/T]CGGCCTCTCTGTTTT	71472
rs213828957	snp	A/G			upstream-variant-2KB, intron-variant	Usp19, Lamb2	GRCm38.p3	9:108489613	TGACTTCCTTAGGAC[A/G]AGGTGATGGGCATGT	71472
rs214645188	in-del	-/GGCTTTTCCAGAGTGCCTAC			intron-variant	Usp19	Mm_Celera	9:108492739	AGGAGAGGTAGGAGG[-/GGCTTTTCCAGAGTGCCTAC]GGCTTCCCTTATCAC	71472
rs214645914	snp	A/G			missense	Usp19	GRCm38.p3	9:108494157	CCGGTTATGGTCCAG[A/G]ACAGAGACCCTGAGC	71472
rs214786243	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108493335	TCCAGGTTACTTTTG[C/T]CACTCTTTTTACAGA	71472
rs214976468	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108497619	CTGCACTTATGTATT[C/T]TTTTCTTCTCTGGAT	71472
rs215799465	snp	G/T			synonymous-codon	Usp19	Mm_Celera	9:108499195	CCGTGAGCAGCGGCT[G/T]GAGGACAAAGGTGCC	71472
rs216085205	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108492222	CCACAACTGCCTTGA[C/T]CTAGCACTTCCTCAG	71472
rs216232291	snp	A/T			intron-variant	Usp19	Mm_Celera	9:108491492	GCTAGTACTAGGTCT[A/T]CGTTCCATCTCCACC	71472
rs216313224	snp	G/T			intron-variant	Usp19	Mm_Celera	9:108501085	TGCTTGATCTGGAAC[G/T]TGGGGGCTTACACCC	71472
rs217058650	in-del	-/G			intron-variant	Usp19	Mm_Celera	9:108491607	AGAGCTGATGATGAA[-/G]GAAGGAACCTGGAGA	71472
rs217601266	snp	A/G			synonymous-codon	Usp19	GRCm38.p3	9:108494231	TGATCCTACAGCCTT[A/G]GTGGAGGGTAACATG	71472
rs218577956	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108495320	CCCGATTGCTCTTCC[A/G]AAGGTCTGGAGTTCA	71472
rs218717825	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108496600	GACTGAAGTCAGAGG[C/T]GTTTGTGTGCACAGG	71472
rs218973861	snp	A/G			intron-variant	Usp19	GRCm38.p3	9:108497690	TCCTTATGGAGGGTC[A/G]GTGAGGTTGATGCCT	71472
rs218992266	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108499035	ACTGCACTGAAGTGT[C/T]GGGAAGGCTGTTCCC	71472
rs219239034	snp	A/T			upstream-variant-2KB, synonymous-codon	Usp19, Lamb2	Mm_Celera	9:108489273	AGCCAGTGAGATTGC[A/T]GAACGCGTCCGAAGC	71472
rs219321484	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108497772	ATATTCCTCTTTTAG[C/T]CCACATATCATGTCC	71472
rs219435214	in-del	-/TTT			intron-variant	Usp19	Mm_Celera	9:108491687	GGAGTCCACTCCTCA[-/TTT]TTTTTTTTTTTTTCG	71472
rs219497611	snp	G/T			intron-variant, utr-variant-3-prime	Usp19	Mm_Celera	9:108501582	GGCAGAGTATCCTAG[G/T]GTGTGTGTCCATCCA	71472
rs219771531	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108491670	TCACCGTGTCTTAAA[A/G]CTGGAGTCCACTCCT	71472
rs219788361	snp	A/G			utr-variant-3-prime, intron-variant, downstream-variant-500B	Usp19	Mm_Celera	9:108502099	GAGGGTGGGAACCTC[A/G]CAAGTTGTGACCTCT	71472
rs219827560	snp	A/G			intron-variant	Usp19	GRCm38.p3	9:108492345	GTAGCCTCACAGTGC[A/G]CATGGCTGCCTCAGC	71472
rs219904437	snp	C/G			intron-variant	Usp19	Mm_Celera	9:108499573	TTGCTGCTTCTGACT[C/G]CTCCTCTGTCGCTCA	71472
rs220488470	snp	A/G			upstream-variant-2KB, intron-variant	Usp19, Lamb2	GRCm38.p3	9:108490020	CCACTGAATTAGTAT[A/G]CCGACCCTGCCTCTT	71472
rs220584907	in-del	-/T			downstream-variant-500B	Usp19	Mm_Celera	9:108502618	CAGCCCAGCTCACTC[-/T]TAACTTCAGTCATAC	71472
rs220877115	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108496748	CGATCTCTCCTGGTG[A/G]CTTCTGTTCCTCAGT	71472
rs220897932	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108494607	TTTGTCCTTCCTCTT[C/T]CTCTGCTCTGCCTCT	71472
rs220904313	snp	G/T			intron-variant	Usp19	Mm_Celera	9:108492800	GTATTGGGGTGGGGG[G/T]GGGGGTCCTGTCTCT	71472
rs220933935	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108491576	AGGTGGGAAACAGAT[C/T]AGGCCTCCGTGGCTC	71472
rs221014964	snp	C/T			missense	Usp19	GRCm38.p3	9:108493777	AGGGCTGTTCACCTC[C/T]GCAGAGGGCCAGAAG	71472
rs221135509	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108493503	GTTCCAGTTGCGTGT[A/G]TGGGAGTTGGGGATA	71472
rs222054656	in-del	-/GTGTGTGTGTG			intron-variant	Usp19	GRCm38.p3	9:108493980	TCTGTTTTTTTTTTT[-/GTGTGTGTGTG]TGTGTGTGTGTGTGT	71472
rs222124457	snp	A/G			upstream-variant-2KB, intron-variant	Usp19, Lamb2	Mm_Celera	9:108489968	AGTGGGTTGGGCGAA[A/G]CCCTCTGGATGGGGT	71472
rs223316563	snp	C/G			downstream-variant-500B	Usp19	GRCm38.p3	9:108502644	CATACCCTTGCCTAT[C/G]GAGTAAATGGTGCTG	71472
rs224068850	in-del	-/T			intron-variant	Usp19	Mm_Celera	9:108497246	TTGTTCTTTTAAACA[-/T]TTTTTATGAGTGTTG	71472
rs224444504	snp	G/T			intron-variant	Usp19	Mm_Celera	9:108497861	AGCTGGAGAAAGGTC[G/T]CACCACATGCCATAT	71472
rs224538581	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108493953	ACTGGCCGGACCAGA[A/G]CTAATCTTGCCTCTG	71472
rs224614046	snp	A/G			synonymous-codon	Usp19	Mm_Celera	9:108495131	CCTGACAGGCCAGGA[A/G]GAAGCCAGGGCTGTG	71472
rs225431972	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108497502	TTTTTTTCTTTTTTT[C/T]TGAGACAGAGTTTCT	71472
rs225551206	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108492425	CCTTGTAGGCAGGGA[A/G]CAGATCACTTGGCCT	71472
rs225607168	snp	C/T			downstream-variant-500B	Usp19	Mm_Celera	9:108502350	CAACATGTTATGGCT[C/T]CCTCCCCGCCCTCCT	71472
rs225758728	snp	C/T			synonymous-codon	Usp19	Mm_Celera	9:108493426	GGCTCGCAAGGGTGG[C/T]CTTCTACAGCTAGTA	71472
rs225855718	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108491845	CACCCGCCTCCACTC[C/T]TAATCTTTAAGGCTG	71472
rs225897307	snp	A/T			upstream-variant-2KB, downstream-variant-500B	Usp19, Lamb2	GRCm38.p3	9:108490574	GGCGGAGGACCTTTA[A/T]ACACGCCATCAGCTG	71472
rs225953914	snp	C/T			downstream-variant-500B	Usp19	Mm_Celera	9:108502800	GTAGACTAGGCTAGC[C/T]TTGAACTCAGAGATC	71472
rs226112041	snp	C/G			synonymous-codon	Usp19	Mm_Celera	9:108498770	CACGTTGCTTTCAAC[C/G]AGCTCTCTGGAGGCT	71472
rs226623763	snp	A/G			synonymous-codon	Usp19	Mm_Celera	9:108494839	ACCAGAGCAGTGTAC[A/G]TTCTGTTTCACGGCC	71472
rs226806119	in-del	-/CCCTCCT			intron-variant	Usp19	Mm_Celera	9:108495968	GCTCACCCCCCCCCC[-/CCCTCCT]CACACACACACACCT	71472
rs227023380	snp	A/C			intron-variant	Usp19	GRCm38.p3	9:108498087	TGGGGGCAGTCACTG[A/C]TGCCTGCCCTTGCTG	71472
rs227083340	snp	G/T			intron-variant	Usp19	Mm_Celera	9:108495295	TGAGATGGCTTAGTG[G/T]GTAAGAGCACCCGAT	71472
rs227146963	snp	C/T			synonymous-codon	Usp19	Mm_Celera	9:108496213	GACTGTGGACTCGGA[C/T]GGGCGGCCCGATGAG	71472
rs227205785	snp	A/C			missense	Usp19	GRCm38.p3	9:108494178	GACCCTGAGCCTGAG[A/C]AAGAAGACCAAGTCA	71472
rs227277962	snp	A/G			intron-variant	Usp19	GRCm38.p3	9:108492891	GGCTTTCCACCTGAG[A/G]GACGTGGCTAAGATT	71472
rs227321552	snp	C/T			synonymous-codon	Usp19	Mm_Celera	9:108499418	TGAAGATCCAGGCTC[C/T]GCTGGTGAGGCTGCC	71472
rs227510732	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108499043	GAAGTGTTGGGAAGG[C/T]TGTTCCCACCAGAGT	71472
rs227819425	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108500436	TATATAAACACGATG[C/T]CACCAGTGTGCACAA	71472
rs228129513	in-del	-/A			intron-variant	Usp19	Mm_Celera	9:108491405	TATTTTTATCACCCC[-/A]CTCTCCCCTAAGGGA	71472
rs228425247	snp	C/G			upstream-variant-2KB, intron-variant	Usp19, Lamb2	Mm_Celera	9:108489099	CAGTCTGAGACCCCA[C/G]AATACCAAGATTGTG	71472
rs228756747	snp	G/T			intron-variant	Usp19	Mm_Celera	9:108492041	CCCTTCTGCTGCTCT[G/T]ACTATTCCTTGGTCT	71472
rs229152634	snp	C/G			intron-variant, downstream-variant-500B	Usp19, Lamb2	GRCm38.p3	9:108491006	CCAGCCCCGACATCT[C/G]GAGCCTCGCGGCGTG	71472
rs229196533	in-del	-/T			downstream-variant-500B	Usp19	Mm_Celera	9:108502717	CAAGTAGTCTTTTTG[-/T]TTTTTTTGTTTTTAT	71472
rs230072691	in-del	-/AAAAA			intron-variant	Usp19	Mm_Celera	9:108495444	TATAATAAATAAATT[-/AAAAA]AAAAAAAAAAAAAAA	71472
rs230961843	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108493292	ACCCCGAGAACAGGG[C/T]TACCTTTGAGTGCTC	71472
rs231368936	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108494294	GCAGGGTTGGTGGGT[A/G]GGCATGGAGTAGTAC	71472
rs231464160	snp	A/C/T			intron-variant	Usp19	Mm_Celera	9:108495968	TGCTCACCCCCCCCC[A/C/T]CACACACACACACCT	71472
rs231491494	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108497786	GTCCACATATCATGT[C/T]CTGCCCCATCTCAGT	71472
rs232079372	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108500296	GGGAGGCCTAACAGG[C/T]TAGTTGGGGGACAGA	71472
rs232084244	snp	A/G			synonymous-codon	Usp19	Mm_Celera	9:108499144	TGTGAATACCCACAC[A/G]CCCCAGTTCTTCATC	71472
rs232567478	snp	A/C			intron-variant	Usp19	GRCm38.p3	9:108492360	GCATGGCTGCCTCAG[A/C]TGGTGAGAATCCTGC	71472
rs232848670	snp	C/T			missense	Usp19	Mm_Celera	9:108498957	CCTATCGAAGGTTGT[C/T]CCTTGCTTGCTGGTG	71472
rs232996141	snp	A/T			upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime	Usp19, Lamb2	GRCm38.p3	9:108490664	AAGCTGCCCTTCACC[A/T]AGAGCTCCCACTCTT	71472
rs233027103	snp	C/T			upstream-variant-2KB, intron-variant	Usp19, Lamb2	Mm_Celera	9:108489763	TTTGTTAAACCTGGG[C/T]CTTTCTGTGGCAGGT	71472
rs233117720	snp	A/C/G			intron-variant	Usp19	GRCm38.p3	9:108491173	GGCAGCATCCTAGCC[A/C/G]GGGCGTTGGTCTGCG	71472
rs233160681	snp	G/T			synonymous-codon	Usp19	Mm_Celera	9:108493369	TCGGCAGTGGGGTGG[G/T]GTCTTCTTTGCTGAA	71472
rs233307144	snp	A/G			intron-variant	Usp19	GRCm38.p3	9:108492915	TAAGATTAATGAGAT[A/G]GGAGTGTCTGGGGTC	71472
rs234153763	snp	C/T			synonymous-codon	Usp19	Mm_Celera	9:108493860	GTCTGACTCAGCTAC[C/T]CAGGTAAGAGTTAGG	71472
rs234192813	snp	C/T			synonymous-codon	Usp19	Mm_Celera	9:108495683	CTGCTTCATGAATAG[C/T]GTCATTCAGTCTTTG	71472
rs235670029	in-del	-/A			intron-variant	Usp19	Mm_Celera	9:108496831	ACTCGTGTGACCCCC[-/A]TGTCACCTCTGCATC	71472
rs235769710	snp	C/T			synonymous-codon	Usp19	Mm_Celera	9:108497164	GAACCTGCGCCTAGC[C/T]GAGGTACCTGTCCTT	71472
rs235832715	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108492299	GGCCTGAAGCACTTG[C/T]CACTGCTTGAATTAT	71472
rs236238799	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108497729	TTTGTCTCAGGTTCT[C/T]TAAAGTGCTTTCTGC	71472
rs236438649	snp	A/G			downstream-variant-500B	Usp19	Mm_Celera	9:108502647	ACCCTTGCCTATGGA[A/G]TAAATGGTGCTGGGC	71472
rs237545753	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108499557	CATGGTGGAGGGAAA[C/T]TTGCTGCTTCTGACT	71472
rs237735678	snp	C/G			intron-variant	Usp19	Mm_Celera	9:108495283	GCTGGGGGCTGGTGA[C/G]ATGGCTTAGTGGGTA	71472
rs237805024	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108496601	ACTGAAGTCAGAGGC[A/G]TTTGTGTGCACAGGT	71472
rs238422285	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108497639	CTTCTCTGGATAAGG[C/T]GTTTGCTAGTAATCC	71472
rs238737578	snp	A/G			missense	Usp19	Mm_Celera	9:108493574	AGAAGAAACCTCTGG[A/G]AACCCAAGAGCTGGT	71472
rs238754595	snp	G/T			intron-variant, utr-variant-3-prime	Usp19	GRCm38.p3	9:108501514	AACTCTGGGCTCTGA[G/T]CCTCAGTGTATGTAT	71472
rs238885262	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108492825	GTCTCTTCCTCCTCT[A/G]TCCTGGTTTGATGGG	71472
rs238969014	snp	G/T			upstream-variant-2KB, downstream-variant-500B	Usp19, Lamb2	GRCm38.p3	9:108490588	ATACACGCCATCAGC[G/T]GTAGGCTACCAGCAG	71472
rs239042029	snp	A/C			intron-variant	Usp19	GRCm38.p3	9:108491823	GATTAAAGGCGTGCG[A/C]CACCACCACCCGCCT	71472
rs239774542	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108491501	AGGTCTACGTTCCAT[C/T]TCCACCCTCACTAGT	71472
rs240123978	snp	C/T			synonymous-codon	Usp19	Mm_Celera	9:108493474	TCTGCTCACGTGGCC[C/T]TCTCTCCTGGTATGT	71472
rs240139707	snp	C/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	Usp19	Mm_Celera	9:108502149	TTAGTAGGCCTTGGC[C/T]TTTCCAGCTGCCTTC	71472
rs240869370	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108496058	CACTAACACTTTGGC[C/T]TCTTCATCTAGGCCA	71472
rs241220385	snp	A/G			missense	Usp19	Mm_Celera	9:108493804	GAAGGGGAAGGGTCC[A/G]TGGATGGCCCCGGCC	71472
rs241274924	snp	A/C			synonymous-codon, intron-variant	Usp19	GRCm38.p3	9:108494681	CCACACCATCTTCCG[A/C]TGGCAGGTGAAGCTC	71472
rs241356441	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108499258	GTACCACCTGCTCTG[C/T]GCAGCTATGTGACCA	71472
rs241798508	snp	C/T			upstream-variant-2KB, intron-variant	Usp19, Lamb2	GRCm38.p3	9:108490246	AGAAAGGTGGGCTTG[C/T]GTGAGAAAAGACTTG	71472
rs242124978	in-del	-/CTGCTGA			intron-variant	Usp19	Mm_Celera	9:108499763	AGCAATGAGTGAGGC[-/CTGCTGA]CTGTGGACAGGGCAC	71472
rs242260699	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108492251	AGTGCAGCCTTCCAG[C/T]GTTGTGGGTTTCTGT	71472
rs242671764	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108494254	GTAACATGGGGACTG[A/G]GCAGGCGGGCCCCCA	71472
rs242916470	snp	G/T			intron-variant	Usp19	Mm_Celera	9:108499055	AGGCTGTTCCCACCA[G/T]AGTGGACAGGTGAGC	71472
rs243148133	in-del	-/AG			intron-variant	Usp19	Mm_Celera	9:108499791	CAGGGCACAGGTATC[-/AG]GGGGCAGCCTGGGCT	71472
rs243563862	in-del	-/AGG			upstream-variant-2KB, intron-variant	Usp19, Lamb2	Mm_Celera	9:108489129	TTCCCAAGGTCATGC[-/AGG]AGGAGAGACTGTTAA	71472
rs244044045	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108493294	CCCGAGAACAGGGCT[A/G]CCTTTGAGTGCTCTG	71472
rs244099301	snp	C/T			synonymous-codon	Usp19	Mm_Celera	9:108494138	CAGGAATGACCCAGT[C/T]GCCCCGGTTATGGTC	71472
rs244413460	in-del	-/AT			intron-variant	Usp19	Mm_Celera	9:108500536	CCCTGGCTCTCCCTC[-/AT]AGTCTCCATATGCTG	71472
rs244549061	snp	A/G			synonymous-codon	Usp19	Mm_Celera	9:108498182	CCAGCGGAAGCAGCA[A/G]TCAGAAGAAGAAAAG	71472
rs244965511	snp	A/C			intron-variant	Usp19	Mm_Celera	9:108492042	CCTTCTGCTGCTCTG[A/C]CTATTCCTTGGTCTC	71472
rs245115800	snp	A/G			downstream-variant-500B	Usp19	Mm_Celera	9:108502833	CCTACCTCTGCATCC[A/G]AGTGCTGGGACTGAA	71472
rs245171938	snp	A/G			upstream-variant-2KB, synonymous-codon	Usp19, Lamb2	Mm_Celera	9:108488756	TCGTCGGCAGGCAGA[A/G]GAGGCACAGCAGCGA	71472
rs245396729	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108497503	TTTTTTCTTTTTTTT[C/T]GAGACAGAGTTTCTC	71472
rs245441673	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108491580	GGGAAACAGATCAGG[C/T]CTCCGTGGCTCAGAG	71472
rs245517801	snp	A/C			intron-variant	Usp19	Mm_Celera	9:108495970	CTCACCCCCCCCCCC[A/C]CACACACACACCTTG	71472
rs246391602	in-del	-/CCC			intron-variant	Usp19	GRCm38.p3	9:108495958	GGTGAGTTGTGCTCA[-/CCC]CCCCCCCCCCCACAC	71472
rs246504591	snp	A/G			intron-variant	Usp19	GRCm38.p3	9:108492132	GAGAGTGAAGGAAGC[A/G]GAGCAGGCTGCTCAG	71472
rs246578844	snp	A/C			intron-variant	Usp19	Mm_Celera	9:108492907	GACGTGGCTAAGATT[A/C]ATGAGATGGGAGTGT	71472
rs246599928	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108497873	GTCGCACCACATGCC[A/G]TATGTGTGTCCTTTC	71472
rs246941426	in-del	-/TTTT			downstream-variant-500B	Usp19	Mm_Celera	9:108502716	CAAGTAGTCTTTTTG[-/TTTT]TTTTTTTTGTTTTTA	71472
rs246999115	snp	C/T			downstream-variant-500B	Usp19	Mm_Celera	9:108502562	CAGGAGGCAGTGGGT[C/T]GCATTCCATGTCAAG	71472
rs248215675	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108491880	GAGAGAGATCGATCC[C/T]TCTTTAGGTGGAAAC	71472
rs248892333	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108497744	CTAAAGTGCTTTCTG[C/T]CCCAGGGCAAGCATA	71472
rs249135133	in-del	-/TG			intron-variant	Usp19	Mm_Celera	9:108493978	CTCTGTTTTTTTTTT[-/TG]TGTGTGTGTGTGTGT	71472
rs249402415	snp	C/G			intron-variant	Usp19	Mm_Celera	9:108491588	GATCAGGCCTCCGTG[C/G]CTCAGAGCTGATGAT	71472
rs249417279	in-del	-/GCGTTGTGGGTTTCTGTAGATACCCAGGAG			intron-variant	Usp19	GRCm38.p3	9:108492250	CAGTGCAGCCTTCCA[lengthTooLong]GCGTGGCCTGAAGCA	71472
rs249449420	snp	A/G			intron-variant	Usp19	GRCm38.p3	9:108497425	GTCGGTGCTTGTAAT[A/G]CTGAGCCATTTTTCC	71472
rs249497945	snp	C/G			intron-variant	Usp19	GRCm38.p3	9:108496775	CAGTCTAGTGCTTTA[C/G]CACTGAAGTTTGCTG	71472
rs249688181	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108500336	TTCAGGTCTACAGAA[C/T]TTATAGACTGGGTTC	71472
rs249982085	snp	C/T			intron-variant, downstream-variant-500B	Usp19, Lamb2	Mm_Celera	9:108491027	TCGCGGCGTGCTCGG[C/T]CTACCGATGCCGACC	71472
rs250072553	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108492304	GAAGCACTTGCCACT[A/G]CTTGAATTATTTATT	71472
rs250579257	snp	C/T			synonymous-codon	Usp19	GRCm38.p3	9:108499156	CACGCCCCAGTTCTT[C/T]ATCTATAAAATTGAT	71472
rs250683073	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108499565	AGGGAAACTTGCTGC[C/T]TCTGACTCCTCCTCT	71472
rs250697920	snp	C/G			upstream-variant-2KB, intron-variant	Usp19, Lamb2	Mm_Celera	9:108489973	GTTGGGCGAAGCCCT[C/G]TGGATGGGGTAGGGG	71472
rs250755209	snp	A/G			utr-variant-3-prime, intron-variant, downstream-variant-500B	Usp19	GRCm38.p3	9:108502077	GGAATTTGGGGGGAC[A/G]TGATTTGAGGGTGGG	71472
rs250876530	snp	A/G			intron-variant	Usp19	GRCm38.p3	9:108492432	GGCAGGGAGCAGATC[A/G]CTTGGCCTTGGCAGT	71472
rs251446371	snp	A/G			synonymous-codon	Usp19	Mm_Celera	9:108494905	TCAGCGCTGGGGGGG[A/G]CTGGAGGCCCCTGCT	71472
rs251619852	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108492367	TGCCTCAGCTGGTGA[A/G]AATCCTGCCCATTAG	71472
rs251678284	snp	G/T			synonymous-codon	Usp19	Mm_Celera	9:108493408	TTCTTGCACCAAAGT[G/T]CAGGCTCGCAAGGGT	71472
rs251862751	snp	A/G			synonymous-codon	Usp19	Mm_Celera	9:108493575	GAAGAAACCTCTGGG[A/G]ACCCAAGAGCTGGTG	71472
rs251958844	snp	A/G			synonymous-codon	Usp19	GRCm38.p3	9:108494431	GAAGGGCCCGGATTC[A/G]GTGGTGGTGCACGTG	71472
rs252047638	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108495792	TCTGTCTCTTACACC[A/G]CTACTTGACTGTTCC	71472
rs252552530	in-del	-/TT			intron-variant	Usp19	Mm_Celera	9:108491688	GGAGTCCACTCCTCA[-/TT]TTTTTTTTTTTCGAG	71472
rs253016623	snp	C/G			intron-variant	Usp19	Mm_Celera	9:108491301	TGTGAATCGGGCCTC[C/G]GTGTAAGGAGGAAAC	71472
rs253156281	snp	A/G			upstream-variant-2KB, synonymous-codon	Usp19, Lamb2	Mm_Celera	9:108489905	GGCAGCATCTACAGC[A/G]GAAGAAACAGCAGGC	71472
rs253381976	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108495308	TGGGTAAGAGCACCC[A/G]ATTGCTCTTCCGAAG	71472
rs253707782	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108499032	GGTACTGCACTGAAG[C/T]GTTGGGAAGGCTGTT	71472
rs253733723	in-del	-/T			intron-variant	Usp19	Mm_Celera	9:108495441	CATATAATAAATAAA[-/T]TTAAAAAAAAAAAAA	71472
rs254545419	in-del	-/C			intron-variant	Usp19	GRCm38.p3	9:108495959	GGTGAGTTGTGCTCA[-/C]CCCCCCCCCCACACA	71472
rs254992782	snp	C/G			intron-variant	Usp19	GRCm38.p3	9:108492252	GTGCAGCCTTCCAGC[C/G]TTGTGGGTTTCTGTA	71472
rs255031900	snp	A/G			upstream-variant-2KB, intron-variant	Usp19, Lamb2	Mm_Celera	9:108490256	GCTTGCGTGAGAAAA[A/G]ACTTGAACTATTTCT	71472
rs255139957	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108494261	GGGGACTGGGCAGGC[A/G]GGCCCCCAGATTGGG	71472
rs255293083	snp	C/G/T			downstream-variant-500B	Usp19	GRCm38.p3	9:108502752	AGACAGGGTTTTTCT[C/G/T]TGTGTAGCCCTGACT	71472
rs256507200	snp	C/G			intron-variant	Usp19	Mm_Celera	9:108497472	TCTTTTTTTCCTTTT[C/G]TTTTTTTCTTTTTCT	71472
rs256516955	snp	G/T			intron-variant	Usp19	Mm_Celera	9:108496625	CACAGGTGTGGTGTT[G/T]CGAGGATAAGTGAGG	71472
rs256670807	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108495285	TGGGGGCTGGTGAGA[C/T]GGCTTAGTGGGTAAG	71472
rs257012591	in-del	-/TT			intron-variant	Usp19	Mm_Celera	9:108497480	CCTTTTCTTTTTTTC[-/TT]TTTTTCTTTTTTTCT	71472
rs257140962	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108498637	GTTCCAAGTGTGACA[C/T]CAGTGGGTCAGAGTT	71472
rs257654055	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108492058	CTATTCCTTGGTCTC[C/T]CTCTCTGCTGCCTGA	71472
rs257851661	snp	A/G			intron-variant	Usp19	GRCm38.p3	9:108491831	GCGTGCGCCACCACC[A/G]CCCGCCTCCACTCCT	71472
rs258001488	snp	C/T			upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime	Usp19, Lamb2	Mm_Celera	9:108490657	CTCCCCAAAGCTGCC[C/T]TTCACCAAGAGCTCC	71472
rs258310513	snp	C/G			intron-variant	Usp19	GRCm38.p3	9:108492839	TATCCTGGTTTGATG[C/G]GGAGAAAAAGATCCA	71472
rs258623483	in-del	-/GGCT			intron-variant	Usp19	Mm_Celera	9:108493289	GTACCCCGAGAACAG[-/GGCT]GGCTACCTTTGAGTG	71472
rs258718671	snp	C/T			missense	Usp19	Mm_Celera	9:108494220	GCACTTGGGGCTGAT[C/T]CTACAGCCTTGGTGG	71472
rs258759316	snp	C/T			synonymous-codon	Usp19	GRCm38.p3	9:108498917	TAGCACCAGTGGACT[C/T]TCTTCTGAGATGCTG	71472
rs258818566	snp	A/G			missense	Usp19	Mm_Celera	9:108500213	AGACCCCCCAGGGCA[A/G]GTCACTCTGAACACC	71472
rs259133082	snp	G/T			intron-variant	Usp19	GRCm38.p3	9:108497678	GAGGCCCTCCGTTCC[G/T]TATGGAGGGTCAGTG	71472
rs259593820	in-del	-/GGC			utr-variant-5-prime, downstream-variant-500B	Usp19, Lamb2	Mm_Celera	9:108490767	TGAAGCAGCGGCGAA[-/GGC]GGCGGCGGTGGCGGA	71472
rs260101023	snp	G/T			synonymous-codon	Usp19	Mm_Celera	9:108496210	AGAGACTGTGGACTC[G/T]GACGGGCGGCCCGAT	71472
rs260223880	snp	C/T			utr-variant-5-prime, downstream-variant-500B	Usp19, Lamb2	Mm_Celera	9:108490776	CGGCGAAGGCGGCGG[C/T]GGCGGAGGAGCCGGG	71472
rs260366849	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108493118	ACCCCTCTGATCTCT[A/G]CCCCTCTCTCCCTGT	71472
rs260409251	snp	A/G			intron-variant	Usp19	GRCm38.p3	9:108499262	CACCTGCTCTGCGCA[A/G]CTATGTGACCATGGT	71472
rs260727153	in-del	-/TTTT			intron-variant	Usp19	Mm_Celera	9:108493969	CTAATCTTGCCTCTG[-/TTTT]TTTTTTTGTGTGTGT	71472
rs260976290	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108496432	TACGGTGGGTTCCCC[A/G]AGAGAGATGCCCCCT	71472
rs261172125	snp	A/G			upstream-variant-2KB, intron-variant	Usp19, Lamb2	Mm_Celera	9:108490018	TTCCACTGAATTAGT[A/G]TACCGACCCTGCCTC	71472
rs261431214	snp	A/G			synonymous-codon	Usp19	Mm_Celera	9:108492660	GCCGCCAGGACTGGA[A/G]GAGGCCACTAGTAAG	71472
rs261535399	snp	A/C			intron-variant	Usp19	Mm_Celera	9:108494983	GTTAGGACCTCCCCG[A/C]GACTTCACACATGCT	71472
rs261575998	snp	C/T			upstream-variant-2KB, synonymous-codon	Usp19, Lamb2	Mm_Celera	9:108489586	AACACAGAGCAGACC[C/T]TGCAGCGGGTATGAC	71472
rs261648638	in-del	-/G			intron-variant, downstream-variant-500B	Usp19, Lamb2	Mm_Celera	9:108490902	TCTCGCTCGGTGAGT[-/G]GTGTGGGCCTCAAGT	71472
rs263625727	snp	A/G			synonymous-codon	Usp19	Mm_Celera	9:108493836	CCAGGGTGATGCCCC[A/G]TCTTTCCTGTCTGAC	71472
rs263734432	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108494730	CCCGTCACTGCTGCC[C/T]TCACTTGGGCTCCCA	71472
rs263768226	snp	A/G			intron-variant, utr-variant-3-prime	Usp19	Mm_Celera	9:108501522	GCTCTGAGCCTCAGT[A/G]TATGTATCTGGTGGG	71472
rs264145324	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108497040	TCTTCCTGTGCCCCA[C/T]GCTGACTTGACCTTT	71472
rs264314019	snp	C/G/T			intron-variant	Usp19	GRCm38.p3	9:108500340	GGTCTACAGAATTTA[C/G/T]AGACTGGGTTCTTCG	71472
rs264587589	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108491963	AAGCAGACTAGATGC[C/T]TTAGTACCAGAGCCT	71472
rs264699243	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108493945	AGGGTACCACTGGCC[A/G]GACCAGAGCTAATCT	71472
rs265335894	in-del	-/T			downstream-variant-500B	Usp19	Mm_Celera	9:108502439	TCAGCACATTTTCTC[-/T]TGGTTATTGTAGAAC	71472
rs265725838	snp	A/G			intron-variant	Usp19	GRCm38.p3	9:108492913	GCTAAGATTAATGAG[A/G]TGGGAGTGTCTGGGG	71472
rs266006150	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108498058	GGGGCCAGCCTGATG[C/T]CACAGGGCCCTGGTG	71472
rs266042861	snp	C/T			downstream-variant-500B	Usp19	Mm_Celera	9:108502587	GTCAAGTGAGGAAGT[C/T]GGGAACACTGAATGC	71472
rs387215435	in-del	-/TGTGGGTTTCTGTAGATACCCAGGAGGCGT			intron-variant	Usp19	GRCm38.p3	9:108492254	GCAGCCTTCCAGCGT[lengthTooLong]GGCCTGAAGCACTTG	71472
rs387579446	in-del	-/GT			splice-acceptor-variant	Usp19	Mm_Celera	9:108494013	TGTGTGTGTGTGTGT[-/GT]AGGTTGAGGCTGAGG	71472
rs578484521	snp	C/G			downstream-variant-500B	Usp19	GRCm38.p3	9:108502436	GGGTCAGCACATTTT[C/G]TCTTGGTTATTGTAG	71472
rs579808320	snp	A/T			intron-variant	Usp19	GRCm38.p3	9:108491768	ACCAGGCTGGCCTCG[A/T]ACTCAGAAAATCCGC	71472
rs581639800	snp	A/C			intron-variant	Usp19	GRCm38.p3	9:108497467	TGTATTCTTTTTTTC[A/C]TTTTCTTTTTTTCTT	71472
rs582277356	snp	A/G			downstream-variant-500B	Usp19	GRCm38.p3	9:108502731	GTTTTTTTTGTTTTT[A/G]TTTTGAGACAGGGTT	71472
rs582756832	snp	A/G			intron-variant	Usp19	GRCm38.p3	9:108491612	TGATGATGAAGGAAG[A/G]AACCTGGAGACAGGG	71472
rs583076158	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108491734	TGTAGCCCTGGCTGT[C/T]CTGGAACTCACTCTG	71472
rs583598438	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108491824	ATTAAAGGCGTGCGC[C/T]ACCACCACCCGCCTC	71472
rs584837415	snp	A/G			intron-variant	Usp19	GRCm38.p3	9:108494006	TGTGTGTGTGTGTGT[A/G]TGTGTGTAGGTTGAG	71472
rs585866654	snp	A/G			intron-variant	Usp19	GRCm38.p3	9:108491732	TGTGTAGCCCTGGCT[A/G]TCCTGGAACTCACTC	71472
rs586857874	snp	C/G			intron-variant	Usp19	GRCm38.p3	9:108491758	CACTCTGTAGACCAG[C/G]CTGGCCTCGAACTCA	71472
rs587019997	snp	A/T			intron-variant	Usp19	GRCm38.p3	9:108495444	TATAATAAATAAATT[A/T]AAAAAAAAAAAAAAA	71472
rs587318687	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108491830	GGCGTGCGCCACCAC[C/T]ACCCGCCTCCACTCC	71472
rs864259212	snp	A/G			intron-variant, missense	Usp19	GRCm38.p3	9:108501219	TTTGGCAGGAGCTCG[A/G]GGCCGAGGAGGAGAT	71472
rs864283328	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108500722	ACACTGTTCCGTAGG[C/T]CCATGAGCACAGTCA	71472
rs864292024	snp	C/T			utr-variant-3-prime	Usp19	GRCm38.p3	9:108502273	CATTTTGGAAGTGAC[C/T]GCTGCTGTTTAAATA	71472