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

Gm35339

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs13459188	snp	G/T	0.410009	0.192086	missense, upstream-variant-2KB	Maf1, Sharpin, Gm35339	Mm_Celera	15:76352871	GAGCCAGGGTGGTGA[G/T]GATGAGAGTCCTCTG	102638882
rs13462858	snp	G/T			utr-variant-3-prime, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76354080	CCCATGCTGTGGCTG[G/T]ATTAAACAGCACGGG	102638882
rs32409698	snp	C/T	0.5	0	intron-variant	Gm35339	Mm_Celera	15:76363475	CTCCCCTGTCTCCCC[C/T]ACCCCCACCCCCAAC	102638882
rs45845677	snp	A/G	0.132653	0.220748	utr-variant-3-prime, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76353989	TGACACCGTCCTGGC[A/G]CTGCCCAAGGCTATA	102638882
rs46094393	snp	A/G	0.231111	0.249285	intron-variant, utr-variant-3-prime	Gm35339	Mm_Celera	15:76358460	AAATAGGCATAGGCC[A/G]ACCACCGATCTCCAC	102638882
rs46206701	snp	G/T	0.132653	0.220748	synonymous-codon	Gm35339	Mm_Celera	15:76361238	GTTGCCTGACATCAC[G/T]GGTAACCTCCGAATC	102638882
rs46455368	snp	C/G	0.124444	0.216185	splice-donor-variant, downstream-variant-500B	Gm35339	Mm_Celera	15:76358631	GGGTCTGACCTGATG[C/G]TAGGTATGAAATCAG	102638882
rs46787577	snp	C/T	0.132653	0.220748	intron-variant	Gm35339	Mm_Celera	15:76361350	CACCTCCACGTATCC[C/T]GACTTAGTCCCAGAA	102638882
rs46912452	snp	C/T	0.124444	0.216185	intron-variant, stop-gained	Gm35339	Mm_Celera	15:76360141	CTCTTCCTAGTTTCC[C/T]AAGCTAAACTGCCCA	102638882
rs47833967	snp	C/T			missense, downstream-variant-500B	Gm35339	Mm_Celera	15:76358944	ATTCCACCCACCTAC[C/T]GGAGGGTGCATAGCC	102638882
rs48380182	snp	C/G	0.152778	0.230321	missense, intron-variant	Gm35339	Mm_Celera	15:76357424	AGCCAAGGAGAAGCC[C/G]GTGCCCTCACCCTCA	102638882
rs48662147	snp	A/G	0.132653	0.220748	intron-variant	Gm35339	Mm_Celera	15:76363440	TAAGTAGACGCAGGC[A/G]TAAGAGCTGGACCCT	102638882
rs49441528	snp	C/G	0.142012	0.225474	synonymous-codon	Gm35339	Mm_Celera	15:76363253	AAGGCCCAATGCTGT[C/G]CTGCGGCCGCGCCGG	102638882
rs49885607	snp	A/G	0.124444	0.216185	synonymous-codon	Gm35339	Mm_Celera	15:76361620	TTCCTGTCCCAGGCA[A/G]GAGCTCAAGAAGCTG	102638882
rs49918178	snp	G/T	0.152778	0.230321	downstream-variant-500B	Gm35339	Mm_Celera	15:76364167	AAGTGGGTCTCAGCA[G/T]AATATTCTCTGCAGT	102638882
rs50356037	snp	A/G	0.244898	0.249948	missense	Gm35339	Mm_Celera	15:76363714	AAGATACATACCCTG[A/G]TGCCTTCAGTTGACC	102638882
rs51314694	snp	A/T	0.132653	0.220748	synonymous-codon, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76353350	TTTCAGCTATAACCC[A/T]GATCTAGACTCCGAC	102638882
rs51422423	snp	A/C	0.132653	0.220748	missense, downstream-variant-500B	Gm35339	Mm_Celera	15:76360727	GAAGCCAGACACAGA[A/C]GTAGGCACTCTAGGT	102638882
rs52291421	snp	A/G	0.32	0.24	intron-variant	Gm35339	Mm_Celera	15:76361891	CCCGAGTTTTTGAAA[A/G]CAGAATCTTCCTTCC	102638882
rs52531626	snp	A/G	0.142012	0.225474	downstream-variant-500B	Gm35339	Mm_Celera	15:76363907	TGTGGGCATGCTTGT[A/G]GAGGCCAAAAATTGC	102638882
rs52704950	snp	A/G			synonymous-codon	Gm35339	Mm_Celera	15:76363187	ggaggaggaggagga[A/G]gaggaggaagaggag	102638882
rs108461097	snp	A/C			intron-variant	Gm35339	Mm_Celera	15:76363483	TCTCCCCCACCCCCA[A/C]CCCCAACCTCAGCCT	102638882
rs212183811	snp	C/G			synonymous-codon, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76353595	ATCCAGTGGCTCCAC[C/G]TACACACCCTCAGAG	102638882
rs212626193	in-del	-/AGGAGA			cds-indel	Gm35339	Mm_Celera	15:76363120	GATCATCGATGGGAG[-/AGGAGA]AGGAGGAGGAGGGGA	102638882
rs213242060	snp	C/T			intron-variant	Gm35339	Mm_Celera	15:76358161	ACTATGGGGTGTTAC[C/T]ACATTCTCAATCCAG	102638882
rs213457986	snp	A/G			intron-variant	Gm35339	Mm_Celera	15:76362420	TGGTTGTGAGCCACC[A/G]TGTGGTTGCTAGGAT	102638882
rs213551377	snp	A/G			synonymous-codon	Gm35339	Mm_Celera	15:76361416	CTGAGTGCAGGACCC[A/G]ACGCAGAAGGAGTTT	102638882
rs213677825	snp	A/G			intron-variant	Gm35339	Mm_Celera	15:76359747	GCCTGAGCCAGGAGT[A/G]TGTCACCAGCGTTTG	102638882
rs213812031	snp	C/G			downstream-variant-500B	Gm35339	Mm_Celera	15:76364248	AAGGGCTTATGCTTC[C/G]CTCTTTCCTTCATTC	102638882
rs214550599	in-del	-/A			intron-variant	Gm35339	Mm_Celera	15:76361384	ACCACGGTCCACCCC[-/A]CCCACCCCCCCTGCT	102638882
rs214594528	snp	C/T			synonymous-codon, upstream-variant-2KB	Gm35339	Mm_Celera	15:76355878	ATTCCCCACCTCTAG[C/T]ATCATCTCAGATCTG	102638882
rs214627656	snp	C/T			intron-variant, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76353830	TAAAGGCCTACTGTG[C/T]GCCAACTTCTGCCTA	102638882
rs214815900	snp	G/T			intron-variant, missense	Gm35339	Mm_Celera	15:76360060	GGAGAGAATGTGTGC[G/T]TGCAGTCAGTGCTCA	102638882
rs214959893	snp	C/T			synonymous-codon	Gm35339	Mm_Celera	15:76358280	GCCCTTCGGCTATTA[C/T]AAGAGATCAGAACCT	102638882
rs215763249	snp	A/G			downstream-variant-500B	Gm35339	Mm_Celera	15:76363924	AGGCCAAAAATTGCT[A/G]TCAAAGTGTTTATTG	102638882
rs215886193	snp	C/T			intron-variant	Gm35339	Mm_Celera	15:76362625	GATGTTTCAAAGGTA[C/T]AGGTGCAAGAGTCCT	102638882
rs216674805	snp	A/T			intron-variant, missense, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76353334	CTCTGCTGTTTTCTC[A/T]TTTCAGCTATAACCC	102638882
rs216960585	snp	A/G			intron-variant	Gm35339	Mm_Celera	15:76357886	CTGCGTCCTGGAAAC[A/G]AAGCTCTATCTGCTT	102638882
rs216993792	snp	C/G			synonymous-codon, upstream-variant-2KB	Gm35339	Mm_Celera	15:76356250	AGGAGAGGTAACTCT[C/G]GGTTGCTGGACCGAA	102638882
rs217265399	in-del	-/C			intron-variant, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76353744	TGGCTGTGGCCATGG[-/C]ACTATCCTCGGGAGC	102638882
rs218208697	in-del	-/CCTT			intron-variant	Gm35339	Mm_Celera	15:76361948	CTTCCTTCCTTCCTC[-/CCTT]CCTTCCTTCCTTTTG	102638882
rs218898313	snp	C/T			intron-variant, synonymous-codon	Gm35339	Mm_Celera	15:76360221	CCATGGTTCTGAAGA[C/T]GCTCCCTGGTAATGT	102638882
rs219739943	snp	A/G			missense	Gm35339	Mm_Celera	15:76363264	CTGTGCTGCGGCCGC[A/G]CCGGGAACGCTGGTG	102638882
rs219772633	snp	A/G			intron-variant	Gm35339	Mm_Celera	15:76361879	CCCCGAGTTACCCCC[A/G]AGTTTTTGAAAACAG	102638882
rs220615169	snp	C/T			synonymous-codon, upstream-variant-2KB	Gm35339	Mm_Celera	15:76356508	GGTCCACCTGGTGTC[C/T]GCTACTACAGGACGA	102638882
rs220782493	snp	A/G			missense, downstream-variant-500B	Gm35339	Mm_Celera	15:76360543	AGCAGTGGTCAAGGC[A/G]CCGAAAGCATTCTTC	102638882
rs220836499	snp	C/T			missense, upstream-variant-2KB	Gm35339	Mm_Celera	15:76356689	CGTCCACCTCCACCT[C/T]CAGCGCCGCAGCCCT	102638882
rs220868574	snp	A/G			downstream-variant-500B, missense, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76354569	GGCTAATAGAAACAG[A/G]CAACCTCTATTCATC	102638882
rs221192488	snp	C/T			downstream-variant-500B, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76354427	GTGGGGCGGGGCCTG[C/T]GTCGTGGGGCGGGGC	102638882
rs221429815	snp	C/G			missense	Gm35339	Mm_Celera	15:76361711	GTTGAGGACTTGAAA[C/G]TTGAATCCAAGGCCA	102638882
rs221927884	in-del	-/CCCAGC			intron-variant	Gm35339	Mm_Celera	15:76357606	AGTGGCTAGAGGGCA[-/CCCAGC]CCCAGCGGGGCTCTT	102638882
rs222069841	snp	A/C			missense, utr-variant-3-prime	Gm35339	Mm_Celera	15:76360351	CCCAACTCTGTGGTA[A/C]TGCGGCAAATGTGGT	102638882
rs222101652	snp	G/T			downstream-variant-500B	Gm35339	Mm_Celera	15:76364353	TTTTGTTTTGGTTTG[G/T]TTTTGGTTTTTTGTT	102638882
rs222311441	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76354194	TTATTGGGCCTGTAC[A/G]CTCCAGCTCTAAGGG	102638882
rs224104370	in-del	-/ACGGACGGA			intron-variant	Gm35339	Mm_Celera	15:76357109	CCTGGGGGGTGGGGG[-/ACGGACGGA]CTCCTGCACTATCCT	102638882
rs224682502	in-del	-/CCCTGATTCTACTGGT			intron-variant, upstream-variant-2KB	Gm35339	Mm_Celera	15:76355043	CCTAGAGATACTGGG[-/CCCTGATTCTACTGGT]CCTTATGAGTTTCCC	102638882
rs226057579	snp	A/T			intron-variant, downstream-variant-500B	Gm35339	Mm_Celera	15:76360753	TAGGTCCTCATGGGG[A/T]GGGTGAGATTGGTGC	102638882
rs226309486	in-del	-/TGAG			downstream-variant-500B	Gm35339	Mm_Celera	15:76364126	GATGCTTCAGTTGTT[-/TGAG]TGTTTTCCTTTATGT	102638882
rs226676212	snp	A/C			synonymous-codon	Gm35339	Mm_Celera	15:76357287	GCGCATCACTGCAGG[A/C]TTTGAGGATCCAGAG	102638882
rs226744822	snp	C/T			missense	Gm35339	Mm_Celera	15:76362850	CTATGGAGCAGGTGA[C/T]GTCTATTGTATCCAT	102638882
rs226948689	snp	C/T			intron-variant, downstream-variant-500B	Gm35339	Mm_Celera	15:76358643	ATGGTAGGTATGAAA[C/T]CAGGCCCAGGCTCTG	102638882
rs226987422	snp	A/G			missense	Gm35339	Mm_Celera	15:76359154	GCCATAGACCTGGAC[A/G]CATCAATCGACTACA	102638882
rs227025006	snp	C/T			synonymous-codon	Gm35339	Mm_Celera	15:76357761	CTATGGAGACCTGGT[C/T]TTCTCACTAGGCTCC	102638882
rs227315826	snp	A/G			intron-variant, upstream-variant-2KB	Maf1, Sharpin, Gm35339	Mm_Celera	15:76353036	GAACAGAAGGGCCCC[A/G]AGCCATGTGGTCCTT	102638882
rs227373585	snp	C/T			intron-variant	Gm35339	Mm_Celera	15:76361795	TGGGCCAAGGGCTGG[C/T]GGTTCACCTACTGGA	102638882
rs227738901	snp	A/G			intron-variant	Gm35339	Mm_Celera	15:76362272	TTGTTTTTGTTTTTC[A/G]AAACAGGGTTTCTCT	102638882
rs227797584	snp	C/T			synonymous-codon	Gm35339	Mm_Celera	15:76361208	AGTGAACATTCTAAA[C/T]TCCCTGCTGAGGTTG	102638882
rs228274986	in-del	-/TTTG			intron-variant	Gm35339	Mm_Celera	15:76362197	TGGTTTTTTTGTTTC[-/TTTG]TTTGTTTGTTTGTTT	102638882
rs228329990	snp	A/G			intron-variant	Gm35339	Mm_Celera	15:76362231	TGTTTTTTCGAGACA[A/G]GGTTTTTTGGTTTTT	102638882
rs228875634	snp	C/T			intron-variant, upstream-variant-2KB	Gm35339	Mm_Celera	15:76355100	CTCGTGCCTCCATTG[C/T]TCACACGTACATCTG	102638882
rs228996855	snp	G/T			intron-variant, upstream-variant-2KB	Maf1, Sharpin, Gm35339	Mm_Celera	15:76352582	TCTGGGGATCAATCT[G/T]TCAGAGATCACTATC	102638882
rs229237178	snp	C/T			downstream-variant-500B, intron-variant	Maf1, Gm35339	Mm_Celera	15:76354735	TTCCTCAGGCTTTAT[C/T]CAGTCCTCAAGGTGT	102638882
rs230488062	in-del	-/G			intron-variant	Gm35339	Mm_Celera	15:76358109	AAAGGCCTCTTGGGA[-/G]TGTATGAGTTCTCTA	102638882
rs230521694	in-del	-/CC			frameshift-variant, intron-variant	Gm35339	Mm_Celera	15:76357462	CTAATCTTAGTTCTG[-/CC]CCCTAGGTCTGTGCT	102638882
rs230559514	snp	G/T			intron-variant	Gm35339	Mm_Celera	15:76359864	GCAAAGTTCAGTGGG[G/T]CCAGTTGTTCAAGAT	102638882
rs230811577	in-del	-/GCA			intron-variant	Gm35339	Mm_Celera	15:76358070	CAGTGGCAGCCTGGG[-/GCA]GCAGGGTTTGCATAG	102638882
rs231410229	in-del	-/C			intron-variant	Gm35339	Mm_Celera	15:76363482	TCTCCCCCACCCCCA[-/C]CCCCCAACCTCAGCC	102638882
rs231991929	snp	C/G			intron-variant	Gm35339	Mm_Celera	15:76362483	GCTCTTAACCACTGA[C/G]CCATCTCGCCAGCCC	102638882
rs232027595	snp	A/G			missense	Gm35339	Mm_Celera	15:76361466	TGCTCCTGGCCTGCA[A/G]CCTGGACGTCCTTGA	102638882
rs233075299	snp	C/T			intron-variant, upstream-variant-2KB	Gm35339	Mm_Celera	15:76356019	GTCAGGCTGGCAGCT[C/T]TTGCAGCCCTTCTCT	102638882
rs233132381	snp	G/T			downstream-variant-500B	Gm35339	Mm_Celera	15:76364335	TTTGCAGTCTGCTGG[G/T]TTTTTTGTTTTGGTT	102638882
rs233618741	snp	C/T			missense	Gm35339	Mm_Celera	15:76361736	AGGCCACCATACGCA[C/T]CCAGTGTCAACAGAA	102638882
rs233936207	snp	A/G			downstream-variant-500B	Gm35339	Mm_Celera	15:76363999	CTCTACATAGTCATT[A/G]CTGGGGCTCGCTATG	102638882
rs234059798	snp	A/C			missense, downstream-variant-500B	Gm35339	Mm_Celera	15:76360693	CTTCCCAAACTTCGG[A/C]GACAGAGCCAGAACA	102638882
rs234133965	snp	C/T			missense	Gm35339	Mm_Celera	15:76357926	TTGTGTCTGAAGGCC[C/T]CTGATGTGATCAGTG	102638882
rs234461497	snp	C/T			intron-variant, synonymous-codon	Gm35339	Mm_Celera	15:76360125	ATCCCGCAAGACTAC[C/T]CTCTTCCTAGTTTCC	102638882
rs234489235	snp	C/T			synonymous-codon	Gm35339	Mm_Celera	15:76361257	AACCTCCGAATCCGG[C/T]TGCAGGCCAAACTCT	102638882
rs234729789	snp	A/T			downstream-variant-500B	Gm35339	Mm_Celera	15:76364168	AGTGGGTCTCAGCAG[A/T]ATATTCTCTGCAGTT	102638882
rs235249816	snp	A/G			intron-variant	Gm35339	Mm_Celera	15:76359225	GGGGCTTTGGTGGTC[A/G]TGTTTTATTCTTACT	102638882
rs235881300	snp	A/G			synonymous-codon, upstream-variant-2KB	Gm35339	Mm_Celera	15:76356529	TACAGGACGAACTGT[A/G]AGTTCACTGCTGTTG	102638882
rs236049260	snp	A/C			synonymous-codon, utr-variant-3-prime	Gm35339	Mm_Celera	15:76360302	CCTCTACATCTAGCT[A/C]CGTTCTCGGCCCATC	102638882
rs236230751	in-del	-/CCCCCA			intron-variant	Gm35339	GRCm38.p3	15:76363471	AATGCTCCCCTGTCT[-/CCCCCA]CCCCCACCCCCAACC	102638882
rs236369297	snp	G/T			missense	Gm35339	Mm_Celera	15:76363222	TACCTGTCTCACTCC[G/T]ACGACGCCACCAGCT	102638882
rs237435362	snp	C/G			synonymous-codon, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76353700	CAGGGCAGAGGAGAC[C/G]AGCACCATGGAGGAA	102638882
rs237540666	in-del	-/G			utr-variant-3-prime	Gm35339	Mm_Celera	15:76363731	GCCTTCAGTTGACCT[-/G]GGGGACAGATAGCCA	102638882
rs237608087	snp	A/C			intron-variant	Gm35339	Mm_Celera	15:76358195	TCTTTTCTCCTGGCT[A/C]CGTCTCACTCCAGCT	102638882
rs237641023	snp	C/T			intron-variant, downstream-variant-500B	Gm35339	Mm_Celera	15:76359046	CACCTTCTAACTCCT[C/T]GTATACCCTAGCTTC	102638882
rs238389471	snp	A/G			missense, downstream-variant-500B	Gm35339	Mm_Celera	15:76360384	CAAGCAGAGGTCAGC[A/G]GTCTTGGCTCCCTAG	102638882
rs238414395	snp	C/T			intron-variant	Gm35339	Mm_Celera	15:76359242	GTTTTATTCTTACTT[C/T]CTATCCCTCCCCAGG	102638882
rs239502500	snp	A/C			missense	Gm35339	Mm_Celera	15:76362667	TCACTCCCCTCTAGG[A/C]GGATACCTTGGAGCA	102638882
rs239959039	snp	A/G			downstream-variant-500B, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76354386	TTAGATGGAACCTGG[A/G]AGTTTGTGGGGGCGG	102638882
rs239981106	snp	A/G			intron-variant	Gm35339	Mm_Celera	15:76363337	ACCGAAGGAAGGTCT[A/G]AACTAAATCCTCTCC	102638882
rs240019683	snp	C/T			intron-variant	Gm35339	Mm_Celera	15:76362079	TCTGCCTCCCAAGCA[C/T]GGGATTAAAGGCCTG	102638882
rs240120961	snp	A/G			missense, downstream-variant-500B	Gm35339	Mm_Celera	15:76360584	CGAAATAAACTATTC[A/G]GTTTGCTCCGACTGA	102638882
rs240160371	snp	C/T			synonymous-codon	Gm35339	Mm_Celera	15:76359168	CGCATCAATCGACTA[C/T]ATGAAGAATAGGGTG	102638882
rs241035454	snp	A/G			missense, downstream-variant-500B	Gm35339	Mm_Celera	15:76358711	CTTTCCTGTACCAGG[A/G]CATAAACCCGGAAAG	102638882
rs241144351	snp	C/T			missense, upstream-variant-2KB	Gm35339	Mm_Celera	15:76356737	AGCCATCTTACAGAT[C/T]CTCGAAGTGCATTCG	102638882
rs241167474	snp	C/T			downstream-variant-500B, intron-variant	Maf1, Gm35339	Mm_Celera	15:76354699	CTAGCATTATTCGGG[C/T]ACCCCTCTAGAAAAC	102638882
rs241361901	snp	A/G			intron-variant	Gm35339	Mm_Celera	15:76361829	CTATTGCCTTCTTCA[A/G]AAAACCATGAGTGGT	102638882
rs241481127	in-del	-/AT			utr-variant-3-prime	Gm35339	Mm_Celera	15:76363834	TATATAAACACACAC[-/AT]ATATATTTATTTACT	102638882
rs242376406	in-del	-/AAAC			intron-variant	Gm35339	Mm_Celera	15:76359645	AGAAGCTCTGTCTCA[-/AAAC]AAACAAACAAACAAA	102638882
rs242954394	snp	A/C			intron-variant, upstream-variant-2KB	Maf1, Sharpin, Gm35339	Mm_Celera	15:76352591	CAATCTGTCAGAGAT[A/C]ACTATCGTGGGCCTC	102638882
rs243547696	snp	G/T			synonymous-codon, upstream-variant-2KB	Gm35339	Mm_Celera	15:76356286	AATCTCTGAGAAAGT[G/T]AGCCATTTGCTGGCT	102638882
rs243921124	snp	A/G			synonymous-codon	Gm35339	Mm_Celera	15:76357365	TTGTGACCACCGACC[A/G]CAGGATGACCCTATG	102638882
rs243922979	snp	C/T			synonymous-codon	Gm35339	Mm_Celera	15:76357506	TAAGATATTTGCCTG[C/T]TCCAGCCTGGATTGC	102638882
rs244341322	snp	A/G			missense, downstream-variant-500B	Gm35339	Mm_Celera	15:76360713	GAGCCAGAACACTGG[A/G]AGCCAGACACAGACG	102638882
rs244663049	snp	A/C			missense	Gm35339	Mm_Celera	15:76363560	AGCAGGGAGCTGACT[A/C]CTGATGGTTCTCTCC	102638882
rs245122032	in-del	-/CTCCCGC			intron-variant	Gm35339	Mm_Celera	15:76361345	AGGGCACCTCCACGT[-/CTCCCGC]ATCCTGACTTAGTCC	102638882
rs245145577	snp	A/C			downstream-variant-500B	Gm35339	Mm_Celera	15:76363922	GGAGGCCAAAAATTG[A/C]TGTCAAAGTGTTTAT	102638882
rs245179744	snp	C/T			intron-variant	Gm35339	Mm_Celera	15:76362490	ACCACTGACCCATCT[C/T]GCCAGCCCAGCAAAA	102638882
rs245436830	snp	A/C/T			intron-variant, stop-gained, synonymous-codon	Gm35339	Mm_Celera	15:76360059	TGGAGAGAATGTGTG[A/C/T]GTGCAGTCAGTGCTC	102638882
rs245751913	snp	C/T			downstream-variant-500B, utr-variant-5-prime, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76354476	AGCAACAGCTGCTGG[C/T]TGCTTTTCAGTTACT	102638882
rs245852275	in-del	-/T			intron-variant	Gm35339	Mm_Celera	15:76362184	TTTTTTTGGTTTTGG[-/T]TTTTTTTGTTTCTTT	102638882
rs246038493	snp	A/G			missense	Gm35339	Mm_Celera	15:76360886	CCCTCCAATTTGGAC[A/G]CTCATTCTTGGAAGA	102638882
rs246219502	snp	A/G			intron-variant	Gm35339	Mm_Celera	15:76357849	TATAGTGAGGTCAAG[A/G]TAGGGAAGGTGGGAC	102638882
rs246250749	snp	A/G			intron-variant, upstream-variant-2KB	Gm35339	Mm_Celera	15:76356119	GCCAAAATGACCTTC[A/G]CCTCTCCTGCAGGTC	102638882
rs246984632	snp	C/T			downstream-variant-500B	Gm35339	Mm_Celera	15:76364095	AGGCATGTGCCACCG[C/T]CCCAGGGCCTATTTT	102638882
rs247182544	snp	A/G			intron-variant, missense, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76353286	TCTTTGCAGCTGGGC[A/G]TGCACATGTGTATGG	102638882
rs247877160	snp	G/T			intron-variant	Gm35339	Mm_Celera	15:76363461	GCTGGACCCTAATGC[G/T]CCCCTGTCTCCCCCA	102638882
rs249383073	snp	C/T			missense	Gm35339	Mm_Celera	15:76359335	GCTACCATAAAGCCC[C/T]ACAGGGTGAGACCTT	102638882
rs249628003	snp	A/T			intron-variant	Gm35339	Mm_Celera	15:76362301	CTGTGTAGTCCTGGC[A/T]GTCCTGGAACTCACT	102638882
rs250553234	snp	C/T			downstream-variant-500B	Gm35339	Mm_Celera	15:76364207	AATGATTGAAACAGG[C/T]GGCATTTGAGGAAAA	102638882
rs251204024	snp	A/C			intron-variant, downstream-variant-500B	Gm35339	Mm_Celera	15:76360498	GTCACATGTTTCTTC[A/C]TGTCCCTCTGCAGGC	102638882
rs251696324	snp	G/T			intron-variant	Gm35339	Mm_Celera	15:76358197	TTTTCTCCTGGCTAC[G/T]TCTCACTCCAGCTTC	102638882
rs251746228	snp	C/T			synonymous-codon, upstream-variant-2KB	Gm35339	Mm_Celera	15:76356688	GCGTCCACCTCCACC[C/T]CCAGCGCCGCAGCCC	102638882
rs252253018	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76354046	GTGGATGTCCACTCA[C/T]CCCTGCAGGCTCCTA	102638882
rs253027220	snp	G/T			downstream-variant-500B	Gm35339	Mm_Celera	15:76364348	GGTTTTTTTGTTTTG[G/T]TTTGGTTTTGGTTTT	102638882
rs253304194	snp	A/G			synonymous-codon	Gm35339	Mm_Celera	15:76358021	TCTACGCGGAGCAGC[A/G]AGCCTCAGGTCTGCT	102638882
rs253654866	snp	G/T			missense	Gm35339	Mm_Celera	15:76361209	GTGAACATTCTAAAT[G/T]CCCTGCTGAGGTTGT	102638882
rs254146285	snp	A/G			synonymous-codon, downstream-variant-500B	Gm35339	Mm_Celera	15:76358618	ACGTTTGGTCTATGG[A/G]TCTGACCTGATGGTA	102638882
rs254769530	snp	C/T			intron-variant, upstream-variant-2KB	Gm35339	Mm_Celera	15:76355014	TCTCTGTGAGGTTTC[C/T]ACTTGGGCTCTTCCC	102638882
rs254995733	in-del	-/TC			intron-variant, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76353571	ATCCTAAGTCCGCTG[-/TC]TCTCTCCCATCCAGT	102638882
rs255175531	snp	A/C			synonymous-codon, upstream-variant-2KB	Gm35339	Mm_Celera	15:76356394	ACCATTAGCACAGCT[A/C]TCCGCACCAGTGCTC	102638882
rs255424668	snp	C/T			synonymous-codon, upstream-variant-2KB	Gm35339	Mm_Celera	15:76355313	TGGGAGCAGGCAAAG[C/T]TGAAGCCTCCTGTCA	102638882
rs255676660	in-del	-/CC			intron-variant, upstream-variant-2KB	Gm35339	GRCm38.p3	15:76355837	GAGCTGAGTCCACTG[-/CC]CCCCCCACCTCCCTC	102638882
rs256183379	snp	A/G			synonymous-codon, utr-variant-3-prime	Gm35339	Mm_Celera	15:76360347	CGTCCCCAACTCTGT[A/G]GTACTGCGGCAAATG	102638882
rs256443462	snp	A/G			intron-variant, downstream-variant-500B	Gm35339	Mm_Celera	15:76359049	CTTCTAACTCCTCGT[A/G]TACCCTAGCTTCTAG	102638882
rs256485081	snp	A/T			missense	Gm35339	Mm_Celera	15:76357747	GCCTTCGCCAGCAAC[A/T]ATGGAGACCTGGTTT	102638882
rs257312614	in-del	-/C			intron-variant	Gm35339	Mm_Celera	15:76361388	GGTCCACCCCACCCA[-/C]CCCCCCCTGCTCCTG	102638882
rs257349455	snp	C/T			synonymous-codon, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76353703	GGCAGAGGAGACCAG[C/T]ACCATGGAGGAAGAC	102638882
rs258122657	snp	A/G			downstream-variant-500B, utr-variant-5-prime, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76354542	GACTGTCTGTGGTAG[A/G]CATGGAGGACAGGCT	102638882
rs258834564	snp	G/T			intron-variant	Gm35339	Mm_Celera	15:76362234	TTTTTCGAGACAGGG[G/T]TTTTTGGTTTTTTTG	102638882
rs259433651	snp	A/C			missense	Gm35339	Mm_Celera	15:76363400	AGGAGGCCAAGGCAC[A/C]AGACTTTGGTGTGTT	102638882
rs259474742	snp	A/G			intron-variant	Gm35339	Mm_Celera	15:76362080	CTGCCTCCCAAGCAT[A/G]GGATTAAAGGCCTGA	102638882
rs259505561	snp	A/G			synonymous-codon	Gm35339	Mm_Celera	15:76360947	TTATTTTGTGGTCCA[A/G]AACTGGTTCAAAAAA	102638882
rs260320939	snp	A/G			intron-variant, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76353549	CCTGGGGCAGCCTGG[A/G]AAAGGAGATCCTAAG	102638882
rs260355066	snp	A/G			missense	Gm35339	Mm_Celera	15:76361756	TGTCAACAGAAGCTT[A/G]AAGACATTTATCTCC	102638882
rs260571172	snp	C/G			synonymous-codon, upstream-variant-2KB	Gm35339	Mm_Celera	15:76356933	CCACAGGTTTCTTCC[C/G]GTGATGGGGCACTCA	102638882
rs260591289	snp	C/T			downstream-variant-500B, intron-variant	Maf1, Gm35339	Mm_Celera	15:76354701	AGCATTATTCGGGCA[C/T]CCCTCTAGAAAACAG	102638882
rs260650605	snp	A/G			downstream-variant-500B, upstream-variant-2KB	Maf1, Gm35339	Mm_Celera	15:76354412	GGCGGGGCCTGCGTC[A/G]TGGGGCGGGGCCTGC	102638882
rs261505822	snp	A/G			missense, downstream-variant-500B	Gm35339	Mm_Celera	15:76358821	ATGATTGTCGGGCAG[A/G]CTGCATTTAGCAATG	102638882
rs261935665	snp	C/T			missense, intron-variant	Gm35339	Mm_Celera	15:76357406	CTGGTGAGCATGGAA[C/T]GGAGCCAAGGAGAAG	102638882
rs264113439	snp	A/T			intron-variant	Gm35339	Mm_Celera	15:76359216	GCAGTTCCAGGGGCT[A/T]TGGTGGTCGTGTTTT	102638882
rs264206948	snp	A/G			missense	Gm35339	Mm_Celera	15:76362669	ACTCCCCTCTAGGCG[A/G]ATACCTTGGAGCAGT	102638882
rs264283619	snp	G/T			intron-variant	Gm35339	Mm_Celera	15:76362242	GACAGGGTTTTTTGG[G/T]TTTTTTGTTTTGTTT	102638882
rs264684300	snp	A/G			intron-variant, upstream-variant-2KB	Gm35339	Mm_Celera	15:76355088	CTGGCAGAAGAGCTC[A/G]TGCCTCCATTGCTCA	102638882
rs264909852	snp	A/G			intron-variant	Gm35339	Mm_Celera	15:76361840	TTCAGAAAACCATGA[A/G]TGGTGCCCGCAGGAA	102638882
rs265963026	snp	A/G			synonymous-codon, downstream-variant-500B	Gm35339	Mm_Celera	15:76360631	GGAGGAGGAAGAGGA[A/G]GAGAGAAGAAAGGAA	102638882
rs266245929	snp	C/T			intron-variant	Gm35339	Mm_Celera	15:76363469	CTAATGCTCCCCTGT[C/T]TCCCCCACCCCCACC	102638882
rs387002890	in-del	-/C			intron-variant, upstream-variant-2KB	Gm35339	Mm_Celera	15:76355844	GTCCACTGCCCCCCC[-/C]ACCTCCCTCCCCACC	102638882
rs387459452	in-del	-/CTTTTCTTTT			intron-variant	Gm35339	Mm_Celera	15:76362155	CTTTTCTTTTCTTTT[-/CTTTTCTTTT]TCTTTTTCTTTTTTT	102638882
rs387896384	in-del	-/TCCTTCCT			intron-variant	Gm35339	Mm_Celera	15:76361947	CCTTCCTTCCTTCCT[-/TCCTTCCT]CCCTTCCTTCCTTTT	102638882
rs578432086	snp	C/T			intron-variant	Gm35339	GRCm38.p3	15:76357104	AGATGGCCTGGGGGG[C/T]GGGGGCTCCTGCACT	102638882
rs579634983	snp	A/G			synonymous-codon	Gm35339	GRCm38.p3	15:76363175	GGAGGAGGAGGAGGA[A/G]GAGGAGGAGGAGGAG	102638882
rs580215971	snp	A/G			intron-variant	Gm35339	GRCm38.p3	15:76361379	AACCCACCACGGTCC[A/G]CCCCACCCACCCCCC	102638882
rs580680187	snp	A/G			intron-variant	Gm35339	GRCm38.p3	15:76358057	GTCTACTTGGCTGCA[A/G]TGGCAGCCTGGGGCA	102638882
rs581142441	snp	C/T			intron-variant, upstream-variant-2KB	Maf1, Gm35339	GRCm38.p3	15:76353567	AGGAGATCCTAAGTC[C/T]GCTGTCTCTCCCATC	102638882
rs581850809	snp	A/G			synonymous-codon	Gm35339	GRCm38.p3	15:76363178	GGAGGAGGAGGAGGA[A/G]GAGGAGGAGGAGGAG	102638882
rs582233576	snp	A/G			missense	Gm35339	GRCm38.p3	15:76363125	TCGATGGGAGAGGAG[A/G]AGGAGGAGGAGGGGA	102638882
rs582575160	snp	A/G			intron-variant	Gm35339	GRCm38.p3	15:76362107	CTGAGCCAATTGCCC[A/G]GCTTTTTTCTTTTCT	102638882
rs583691626	snp	C/T			intron-variant	Gm35339	GRCm38.p3	15:76362137	TTTTCTTTTCTTTTC[C/T]TTTCTTTTCTTTTCT	102638882
rs584602920	snp	C/T			intron-variant, upstream-variant-2KB	Gm35339	GRCm38.p3	15:76355064	TTCTACTGGTCCTTA[C/T]GAGTTTCCCTGGCAG	102638882
rs584980921	snp	C/T			intron-variant	Gm35339	GRCm38.p3	15:76362136	CTTTTCTTTTCTTTT[C/T]TTTTCTTTTCTTTTC	102638882
rs585281520	snp	A/G			intron-variant	Gm35339	GRCm38.p3	15:76358117	CTTGGGAGTGTATGA[A/G]TTCTCTACACTCCCA	102638882
rs585728249	snp	A/G			synonymous-codon	Gm35339	GRCm38.p3	15:76363166	GGAAGAGGAGGAGGA[A/G]GAGGAGGAGGAGGAG	102638882
rs864284125	snp	A/T			utr-variant-3-prime, upstream-variant-2KB	Maf1, Gm35339	GRCm38.p3	15:76354341	TCACTTTGCTGCAGC[A/T]CATTTGTTTCCAATA	102638882