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

Psen2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs258315197	snp	C/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180264525	TTGTACATGCCTCAG[C/T]GCCAATAACTAAACA	19165
rs258376999	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180241325	AGCATCAAAACACGG[A/G]GCTGCCTCAGTACCT	19165
rs258396512	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180235988	GATGAACTGGATAAC[A/G]GAAACAAGAGGACCA	19165
rs258439988	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180233462	ACCCTCCTGCAGGTG[A/G]CGACCTCAGTGTTAT	19165
rs258444730	snp	A/G			downstream-variant-500B	Psen2	Mm_Celera	1:180226974	CCCCTCTCACTACAC[A/G]GCGGAGAACAAAGGG	19165
rs258456804	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180228269	GTCTGTTATCCCATC[C/G]CTGACACACATGTGG	19165
rs258462185	in-del	-/CCCCCCCCCG			intron-variant	Psen2	Mm_Celera	1:180250804	CTAGGGAAGGGTTTC[-/CCCCCCCCCG]CCCCCCAAACAGGGT	19165
rs258604962	in-del	-/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264800	TTTGTTTATCTTCTG[-/T]TTTTTCTCCCCCACG	19165
rs258638853	in-del	-/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257448	GCTCAACATCTTGAA[-/T]TTTTTTCCTTAACAC	19165
rs258665893	snp	C/T			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247529	ATTCAGCCTAGGTAT[C/T]TCCTAGGAGGGCAGA	19165
rs258728943	snp	A/C			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255967	TACGCTCCTTCCAAG[A/C]CCCAGTTCTGGGCCG	19165
rs258741616	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180236742	CCCACTTTCCAATGT[A/G]GCCACATTGGGTAAA	19165
rs258769730	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180232337	CTTCAGGAAGATGGG[C/T]CATTGTGTCACACTG	19165
rs259008990	in-del	-/AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG/CA			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259117	CACACACACACACAC[lengthTooLong]AGAGCCTTTATATTT	19165
rs259292029	snp	A/G			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258906	GTCGGAGGTGTGGTG[A/G]TTTGAATATGCTTGG	19165
rs259460493	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180239791	TAGCTAATCTTTGTT[A/G]TATAAGCCAATCTAA	19165
rs259465069	snp	A/G			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258949	GCCACTATAAGAGGA[A/G]TGCCCTTATTGGAGG	19165
rs259514364	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180231718	TTCACTTATCCCAGG[G/T]TCCTCAAGGCTCGCC	19165
rs259547039	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180231793	ATACTCTGTTGTATG[A/G]AATTACCATATTTCA	19165
rs259585316	in-del	-/TGTTG			intron-variant	Psen2	Mm_Celera	1:180252055	TGTTTTGTTTTGTTT[-/TGTTG]TTGTTGTTGTTGTTG	19165
rs259702483	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262499	ATAGTTTTGAGTCCT[A/G]TAACTAAGGGGGTTT	19165
rs259707357	in-del	-/ATCTTTGTC			intron-variant	Psen2	Mm_Celera	1:180230356	TCCAAGTAAGAAATA[-/ATCTTTGTC]GTCTAGAACTACTTT	19165
rs259724792	snp	A/T			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246744	CACAGGACTTCTGCA[A/T]GGTTCTCAATAATGT	19165
rs259828245	snp	A/C			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260620	AGAGAATCAATTCTA[A/C]TTTAGAGAAATTTGT	19165
rs259907440	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180235452	GGTGGGCCACATGAC[C/T]ATGTGATGGACCCAC	19165
rs259956051	in-del	-/A			intron-variant	Psen2	Mm_Celera	1:180231739	AGGCTCGCCCATATC[-/A]ACGTGGGTCAGAGTT	19165
rs259969799	snp	A/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264272	TCCCTCCTTCACCCT[A/T]TCCCACCCGACCATG	19165
rs259984836	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180227815	CCGAACGGCCACAGA[C/T]ATGTGCTGTCTCTTA	19165
rs259993493	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180252834	ACAGGAAGGCGGTCA[C/G]CCTTTCATCCCCTTC	19165
rs260018397	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180250551	CAGTGGCCCCGGCAG[G/T]AAAGAGATTTCGGAA	19165
rs260057757	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180239576	ATTGCTGCTGCTGCT[A/G]CCTCCACCACCACCA	19165
rs260077355	snp	A/T			intron-variant	Psen2	GRCm38.p3	1:180239792	AGCTAATCTTTGTTG[A/T]ATAAGCCAATCTAAT	19165
rs260079732	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180251034	CTTGAAATACCTGGG[A/T]TGGAGCAATTTTTCT	19165
rs260122801	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180231634	CCCACTCTATTTTAC[A/G]TCTGTGACTTTGCCT	19165
rs260144916	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180240329	ATACTTAAGGGGGCA[A/G]AGACCCAGGCAGGAC	19165
rs260225285	in-del	-/C			intron-variant	Psen2	Mm_Celera	1:180250362	GGGACTAAGGACCTA[-/C]CTACCCTCTGCCGAC	19165
rs260259575	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180233116	CAAATACATGTATAA[A/T]CCCACATCCCTCTGA	19165
rs260318970	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180237835	CAGGAACATGTCCTG[G/T]GACTCCTTTCCATGG	19165
rs260366368	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180249548	GCTTTGAACTTCTGA[C/T]CCTTCTGCCTCCACC	19165
rs260369033	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180230165	AAGCAACACTGGCAA[A/T]AATGGTGCTCAGTGA	19165
rs260423499	in-del	-/AA			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254443	GTGATAACCACTGGG[-/AA]AAAAATGGCTCTTTA	19165
rs260509345	in-del	-/C			intron-variant	Psen2	Mm_Celera	1:180238541	AAGATTGAAAATAAG[-/C]CCCAGAGAGAAGGTC	19165
rs260670189	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180234465	TCCTGCACCATGCCT[A/G]CCTGCACGCTGCCAT	19165
rs260715783	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259980	TGAGATATCTACAAA[A/G]CATACTTCTGGGATA	19165
rs260717292	snp	C/T			downstream-variant-500B	Psen2	Mm_Celera	1:180226828	TTGTCCCAATACCTC[C/T]CAATGCCCTGTTATG	19165
rs260781181	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257148	TCCCAGCACCGGAAA[A/G]GCAGAGACAGGCACA	19165
rs260910537	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180256783	TCGGGGTGAGGGCAG[A/G]GAGGGGTTGTGATCG	19165
rs260959940	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180248930	CTGGTACAGGAACTC[C/G]CTCCTCCTCCCCCTC	19165
rs261073495	in-del	-/A			intron-variant	Psen2	Mm_Celera	1:180230679	TAAAAATGTAACCAT[-/A]AGGGGTTAGAGAGAG	19165
rs261136894	in-del	-/CT			intron-variant	Psen2	Mm_Celera	1:180252258	TCCAGACCCAAGGGC[-/CT]TCTGAGCCCCTCTCA	19165
rs261177407	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180252193	GGGATTAAAGACGTG[C/T]GCCACCACCACCCAG	19165
rs261190701	snp	G/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262708	GCTCTCCTCGGGGAG[G/T]ACAGACTGTCTGTGG	19165
rs261198433	in-del	-/G			intron-variant	Psen2	Mm_Celera	1:180236570	TACATCAGAATGAAA[-/G]GGAAGTCCAGGCAAG	19165
rs261225498	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180252928	TGTCGCCCTAAGGAG[A/G]CCTTAACTTTCCTGA	19165
rs261251831	snp	A/G			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254644	TGACACAGCGGCAGC[A/G]GCAGCCTCTGGCAGC	19165
rs261258767	snp	A/G			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258543	TAATGTTTAGACTTC[A/G]TAAAATACAAAAAGA	19165
rs261275546	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244761	CACTGCACACTGTGT[C/T]TGTGTAGTCTATTAC	19165
rs261337566	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180244482	AGCCCACTGCACACT[A/G]TGACTGTGTAGCCCA	19165
rs261448006	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180229348	AGGTATTTTTAAATA[A/C]ACTTGTGAAGCAGGC	19165
rs261634543	snp	C/T			utr-variant-3-prime, nc-transcript-variant	Psen2	Mm_Celera	1:180227178	TGGTCAGGGTGATGG[C/T]GCCTCCTGGTTCCCA	19165
rs261674687	in-del	-/G			intron-variant	Psen2	Mm_Celera	1:180233496	AAGACCCTCATCTTT[-/G]GTTAAGATAGAATAT	19165
rs261981339	snp	A/G			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254422	TAGTACGTTTTTATA[A/G]TAACTGTGATAACCA	19165
rs261994452	snp	A/C			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258207	CTTGTTGATCTCATC[A/C]ATGAGGCCTGTGTTC	19165
rs262053593	snp	G/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180256798	GGAGGGGTTGTGATC[G/T]CAGGATCGGTCTGTG	19165
rs262086893	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180249065	TCGCTGCAGTATATT[A/G]CTGCAATTGCTGGTT	19165
rs262125034	in-del	-/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180256678	CCTTCTCCTGATTGA[-/T]TTTTTTCCAGAGTGC	19165
rs262151789	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180241764	CTGCACATGGTGACT[A/G]TGTAGCCCACTGCAC	19165
rs262251608	in-del	-/GC			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255617	ACTAGCTCTTGCTTT[-/GC]CGAGTTCCTTCGGTT	19165
rs262307302	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180253846	TATATACATGTAGCA[A/C]TGTCCAAATCCTGTG	19165
rs262337151	snp	C/T			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246072	CCGGAGCTCTAGCCT[C/T]GAATAAGTAAACCCT	19165
rs262376864	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180250047	ACCCCTAAGGGCCGG[C/T]CTGCAAGGCCTCTGT	19165
rs262412262	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180239416	TGCCTTAGGGTGGGT[C/T]TGTGAGGGTATTTCT	19165
rs262519944	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180248336	CAAGATAATTCTCAA[A/G]GGCTCATCTCCTAGG	19165
rs262614835	snp	C/T			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247943	TGGCAGAGCCTGCCA[C/T]GCCTGAGGCCTTGGG	19165
rs262644733	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180237414	ACTTAAGGACTGTCC[A/G]CGGTCACCAGCTCAG	19165
rs262709334	snp	C/T			missense, nc-transcript-variant	Psen2	Mm_Celera	1:180240911	GCGTAGCGGTCCGGG[C/T]CCTCTTCACAGTCTT	19165
rs262744865	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180232876	GGGCATGCTGCAGGC[A/G]ATTCTCCACTCTAAG	19165
rs263106405	in-del	-/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180265084	GGGAGGTTGTCCATC[-/G]GGTCTACAAAAGGCA	19165
rs263283853	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180249739	CCTACCGATTTTTCT[C/T]CTCTTGAGATAAGGT	19165
rs263369461	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180240221	GCTCACAGTTCTCTG[A/T]ATTATATTTATTAAG	19165
rs263412064	in-del	-/T			intron-variant	Psen2	Mm_Celera	1:180232389	CCAGACCTTCCCCTC[-/T]CTACCTTTCCTGTCT	19165
rs263460699	snp	G/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180263031	TGTGAAGTGAAAATT[G/T]GCACCCAGGAAGGAA	19165
rs263472156	snp	C/T			synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180245701	GGCTGACATCAAGGA[C/T]GTCCGCTCATCACAC	19165
rs263507826	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180234982	CCACCAGGCCCAAGC[A/G]ACCTACCGTACACAG	19165
rs263536574	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180236057	AGATACTTCCATCCA[C/T]CCTTCCCTTTGACCA	19165
rs263569898	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180228456	CATCAGAGCCTCCAG[A/G]CTACTGCTGGGGTTG	19165
rs263579712	in-del	-/T			intron-variant	Psen2	Mm_Celera	1:180250726	CAAAAGGTCACCTTC[-/T]GGGGTCACATGGCTA	19165
rs263595182	in-del	-/C			intron-variant	Psen2	Mm_Celera	1:180241575	CAGGCCATCTCAGCA[-/C]ATGGTTACCCCATCT	19165
rs263674770	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244196	TGTGATTGTGTAGCC[C/T]ACTGCACACTGTGAC	19165
rs263704935	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180232239	CCCCACAGTCTCCAC[C/T]GGGCCCTTCCTGGGT	19165
rs263729083	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180233937	AGGCTCGGAAGTCTT[C/T]CTTCCCGAAGCCTCA	19165
rs263822885	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180238464	AGATCCAAAGGAGAA[C/G]CCAACTCACAGGCTT	19165
rs263855050	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180230710	GGCTGTGGTTAAAAA[A/C]CGCTTGAAGAGGTCC	19165
rs263868168	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180238197	GATAGCCCAGAGGGT[A/G]AAGGTGCTTGCTGCC	19165
rs263888198	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180230343	GAACGTCACTGCCTC[C/T]AAGTAAGAAATAATC	19165
rs263924424	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259322	GCTGCTCTGCTTCTT[C/T]TTCCTGCATGTTTTT	19165
rs263936257	snp	C/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262856	AGACAGCTGCAGAGG[C/G]AAGACCCCTCAGATA	19165
rs264070038	snp	A/C			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264609	ACGACATTACCATAG[A/C]GATCCCTGTAGAGAC	19165
rs264129400	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259373	TCTCTCCTCTCCTGC[A/G]CACACTCCTAAAGCA	19165
rs264220766	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180253681	CCCAACCAGGGCTAC[A/G]CACCAAAACCCTGTC	19165
rs264240001	in-del	-/CTAC			intron-variant	Psen2	Mm_Celera	1:180241593	GGTTACCCCATCTGG[-/CTAC]CTACCTACCTGAACC	19165
rs264341566	in-del	-/C			intron-variant	Psen2	Mm_Celera	1:180230943	TGTCAACTAACCAGA[-/C]CCCCCCCCAGAGCTC	19165
rs264380276	snp	A/T			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258787	TTCTCACGAGGTAGA[A/T]GAACAGATGAGCAAA	19165
rs264501858	snp	G/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261443	CAATTTCTAGTCTTG[G/T]ATAATTTCACCTCTT	19165
rs264508119	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260375	CTCTGATTCTCTAGG[C/T]TAATCTTAAGTCCTG	19165
rs264527987	snp	A/G			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255902	GGGTTCTGGAGGCAG[A/G]AAGGGACGCGAGGGC	19165
rs264561845	in-del	-/AG			intron-variant	Psen2	Mm_Celera	1:180230835	TGCAGGCAAACTAAC[-/AG]ATTTGCAGGGCAAAT	19165
rs264581941	in-del	-/T			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258522	TTTAAAAATTAGGTA[-/T]TTTTTTAATGTTTAG	19165
rs264615881	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180232982	ATCACAGGCTCTATA[C/T]TCAGATAGCGGCCAC	19165
rs264649574	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180230199	GCTTGGTGAACTGCA[A/T]CTTTAAAAACGTGTC	19165
rs264669168	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180234109	GGCTGCTTGATGAGC[A/G]GCAAATGTGGGCAGT	19165
rs264685767	snp	A/T			downstream-variant-500B	Psen2	Mm_Celera	1:180226538	GGGCAGTAGCTTCTG[A/T]GGTCTCACGTCCCCA	19165
rs264724141	in-del	-/C			utr-variant-3-prime, nc-transcript-variant	Psen2	Mm_Celera	1:180227438	CGACACGTTTTTATT[-/C]TTTTTTTTTTTTTCT	19165
rs264863762	in-del	-/GGGTG			intron-variant	Psen2	Mm_Celera	1:180238659	AGCACAGAAGACAGT[-/GGGTG]GGGGGGGGGCGTACA	19165
rs264933651	snp	C/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257518	GCATGAACGGAGGTC[C/T]GAAATCTCCCTCTTC	19165
rs264949717	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180249600	GTATGAACCTCTACA[C/T]CCAGTTCACGATGTA	19165
rs265008304	in-del	-/T			intron-variant	Psen2	Mm_Celera	1:180252535	GGGTAGTTTACTTTG[-/T]CTTCAGATTTATAAG	19165
rs265013111	in-del	-/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180257896	CTTGAAAAAGCCCAA[-/T]TGTGCTGTAATGGAG	19165
rs265038298	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244996	ATCTATTCATCCATC[C/T]GTGTGTGGACACATA	19165
rs265040531	in-del	-/CAGATATAT			intron-variant	Psen2	Mm_Celera	1:180254245	TATGTCTGTCTAGAA[-/CAGATATAT]CTGTGTAGTACATTT	19165
rs265071982	snp	C/T			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246978	GCCACTCTTAGAATT[C/T]GTGTGATCTTCAAGT	19165
rs265092117	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180251190	TCTCACTGTATATAG[C/T]TCTGGCTGTCCTGGA	19165
rs265214528	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180248704	GGAAGATCTGGGCAT[C/T]TGATGCAGGGGGGTA	19165
rs265231292	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180238059	AACCAGGGTCTAAAA[C/G]CTGGTGGCACAGTTA	19165
rs265301646	in-del	-/AGA			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261539	CCTGGCTTAATACAG[-/AGA]AGATTACACAGGACA	19165
rs265382540	snp	C/T			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254815	GCTTCCAGCTCAGTC[C/T]GCACCTCCACTCACC	19165
rs265575900	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180250406	AGGGCTGGAAACAGA[A/T]GTTGATTAGCTGAAC	19165
rs265664456	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246137	GACAAATGGCACATC[A/G]ACAGAGGATGAAGGA	19165
rs265713040	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180237193	GGTCCAAATGTCAGG[C/G]AGCTCACTGGCCGCT	19165
rs265732480	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180241140	AGGGTCAGAGCTAGC[C/T]TGCATAGCCACAGAA	19165
rs265749688	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180233081	ACACACAGGAGCTAC[C/G]GGTAAGTAGGAACAT	19165
rs265793566	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261896	GATGCAGCCATCTGC[A/G]GCATCCCTCTAAAAC	19165
rs265853918	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180238726	AGTGCCAGAGAGCAC[A/G]AAGAGGCAATCTATT	19165
rs265869997	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180231070	AGGAGAAGCTCTTGG[C/T]TCTGTGGAAGCTCAA	19165
rs265888086	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260561	GATAGATGGATGGAT[A/G]GATGGATAGATAGAT	19165
rs265933343	snp	A/C			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180265457	GTGATATAGAAGAAT[A/C]ACTTAGATAAGGTGA	19165
rs265939691	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180229293	GGAGAGACCACTGGG[A/G]CTGCAGGCTGCGGTG	19165
rs266108827	in-del	-/TTCTTC			cds-indel	Psen2	Mm_Celera	1:180227450	ATTCTTTTTTTTTTT[-/TTCTTC]TTCTTCTTTTGTAAG	19165
rs266203795	snp	A/C			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259662	TCCTCACTGCCTGCA[A/C]ATTGCCATACACTCT	19165
rs266231710	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180232472	CCAAGCCTACCTCGG[A/G]GTCTTTGTACCAGCT	19165
rs386890771	in-del	-/C			intron-variant	Psen2	Mm_Celera	1:180251421	GAGCTATTTCCCCCC[-/C]TCTATGAACAGCAGG	19165
rs386940532	in-del	-/TT			intron-variant	Psen2	Mm_Celera	1:180249435	GATTTTTTTTTTTTT[-/TT]GGCTTTGTATTTTTC	19165
rs386973685	in-del	-/A			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264453	GTAAGAAAAAAAAAA[-/A]TCTACCCCAAAACAC	19165
rs387011325	in-del	-/TT			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258596	TTCATCTTTTTTTTT[-/TT]CTAATACCCCTTTGG	19165
rs387033382	in-del	-/ATCTG			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261963	TTCCCTCGATGCCTG[-/ATCTG]TAAGCCTAAGGCAAA	19165
rs387096876	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	Psen2	Mm_Celera	1:180227451	TTCTTTTTTTTTTTT[-/T]CTTCTTCTTCTTTTG	19165
rs387107960	in-del	-/CACACACACACACACACACACACA			intron-variant	Psen2	Mm_Celera	1:180248241	ACACACACACACACA[-/CACACACACACACACACACACACA]GAGTCCGGACTGTGC	19165
rs387181854	in-del	-/NNCTATCTATCT			intron-variant	Psen2	GRCm38.p3	1:180244972	TCTATCTATCTATCT[-/NNCTATCTATCT]ATCTATCTATCTATT	19165
rs387186065	snp	A/T			intron-variant	Psen2	GRCm38.p3	1:180244735	CCACTGCACACTGTG[A/T]CTGTGTAGCCCACTG	19165
rs387196316	in-del	-/C			intron-variant	Psen2	GRCm38.p3	1:180251416	GGCAGGAGCTATTTC[-/C]CCCCCTCTATGAACA	19165
rs387262772	in-del	-/CT			intron-variant	Psen2	Mm_Celera	1:180252262	AGACCCAAGGGCTCT[-/CT]GAGCCCCTCTCAGTC	19165
rs387344111	in-del	-/C			intron-variant	Psen2	Mm_Celera	1:180250810	AAGGGTTTCCCCCCC[-/C]AAACAGGGTACGCCC	19165
rs387352580	in-del	-/TCTCTCTGTCTCTCTGTCTCTCTGTCTCTCTGTCTCTGTC			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263158	CTCTCTGTCTCTCTG[lengthTooLong]TCTCTCTCTCTCTCT	19165
rs387491024	in-del	-/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180257897	TTGAAAAAGCCCAAT[-/T]GTGCTGTAATGGAGG	19165
rs387506147	in-del	-/TCTCTCTCAC			intron-variant	Psen2, Gm31728	Mm_Celera	1:180263210	GTCTCTCTCTCTCTC[-/TCTCTCTCAC]ACACACACAGATAGA	19165
rs387519305	in-del	-/TA			intron-variant	Psen2	Mm_Celera	1:180249361	ACACACACACACACA[-/TA]GGACTTGGAAAACTA	19165
rs387548472	in-del	-/GG			intron-variant	Psen2	Mm_Celera	1:180238672	TGGGTGGGGGGGGGG[-/GG]CGTACAGTTTAAAAG	19165
rs387600664	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244736	CACTGCACACTGTGA[C/T]TGTGTAGCCCACTGC	19165
rs387607749	in-del	-/A			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260987	GGGGCTGAGAGAAAA[-/A]TGTCTGGGAGGATTA	19165
rs387631877	in-del	-/TTA			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246996	GTGATCTTCAAGTGA[-/TTA]GACAGGGTCCCTTCA	19165
rs387636899	in-del	-/TT			intron-variant	Psen2	Mm_Celera	1:180251152	TTTTTTCCTTTCTTT[-/TT]GTTTTGTTTTTTGAG	19165
rs387663004	in-del	-/TCGGACAAC			intron-variant	Psen2	Mm_Celera	1:180248068	TGTTGTGGTAAGTAC[-/TCGGACAAC]ACAGTTCAAGAGTTT	19165
rs387716525	in-del	-/A			upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180264115	CACACAAACAAACAG[-/A]AAAAAAAAAATGGAG	19165
rs387762532	in-del	-/CACACACACA			intron-variant	Psen2	Mm_Celera	1:180253304	ACAGACACACACACA[-/CACACACACA]GTGTTATGGTTCCTT	19165
rs387852025	in-del	-/A			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264125	AACAGAAAAAAAAAA[-/A]TGGAGAGCAAAGCTT	19165
rs387860040	in-del	-/C			intron-variant	Psen2	Mm_Celera	1:180243580	TAGCCCACTGCACAC[-/C]TGTGATTGTGTAGCC	19165
rs578283075	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180243875	ACTGTGTAGCCCACT[A/G]CACACTGTGACTGTG	19165
rs578305797	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180237003	AGAGGCGAGAGTCCT[A/G]AGGGTCTGCTGACCC	19165
rs578306794	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180250816	TTTCCCCCCCAAACA[A/G]GGTACGCCCTGCGAC	19165
rs578634970	snp	A/T			intron-variant	Psen2	GRCm38.p3	1:180237669	AGCACGGTCATTCCC[A/T]TGCTGTTCCTAGTTT	19165
rs578637970	snp	C/G			intron-variant	Psen2	GRCm38.p3	1:180253275	ACACACACACACACA[C/G]ACACACACAGACACA	19165
rs578824101	snp	C/G			intron-variant	Psen2	GRCm38.p3	1:180244530	GTAGCCCACCGCACA[C/G]TGTGACTGTGTAGCC	19165
rs578827168	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180242147	TGTGACTGTGTAGCC[C/T]ACTGCACATGGTGAC	19165
rs578834681	snp	C/G			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263195	TGTCTCTCTGTCTCT[C/G]TCTCTCTCTCTCTCT	19165
rs578876516	snp	C/G			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263181	TCTCTCTGTCTCTCT[C/G]TCTCTCTGTCTCTGT	19165
rs578906402	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180241840	CATACACTGTGATTG[C/T]GTAGCCCACTGCACA	19165
rs579188713	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180228697	TATGGTGAGTGAGAT[C/T]CAAGCCTCCCACTCC	19165
rs579214315	snp	C/G			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263173	TCTCTCTGTCTCTCT[C/G]TCTCTCTGTCTCTCT	19165
rs579232663	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244571	TGTGATTGTGTAGCC[C/T]ACTGCACACTGTGAC	19165
rs579250243	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180241807	TAGCCCACTGCACAT[G/T]GTGACTGTGTAGCCC	19165
rs579399899	snp	C/G			intron-variant	Psen2	GRCm38.p3	1:180253293	ACACACAGACACACA[C/G]ACACACACACAGTGT	19165
rs579432747	snp	A/C			intron-variant	Psen2	GRCm38.p3	1:180237504	CTGAGAAGGAAGGGA[A/C]GGCGTGGCCTTTATA	19165
rs579461656	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180243958	GCCCACTGCACACTG[G/T]GACTGTGTAGCCCAC	19165
rs579585678	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180233207	CTAAGCCACTGTCCA[C/T]GAACCCCAGAGGGAA	19165
rs579609815	snp	G/T			intron-variant, upstream-variant-2KB	Psen2	GRCm38.p3	1:180247819	TTTGAGAACTGGCTG[G/T]CTGTCATATCTTAAA	19165
rs579718469	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180242277	CTGTGTAGCCCACCG[C/T]ACACTGTGACTGTGT	19165
rs579722620	snp	A/T			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263214	CTCTCTCTCTCTCTC[A/T]CTCACACACACACAG	19165
rs579971194	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244676	TTGTGTAGCCCACTG[C/T]ACACTGTGACTGTGT	19165
rs579998301	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180231469	ATGCTCATACAGACA[C/T]GTATGCACACCCAAA	19165
rs580011578	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244728	GTGTAGCCCACTGCA[C/T]ACTGTGACTGTGTAG	19165
rs580015069	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180230430	AGCTTTCACACTGAC[C/T]GGTTGAACCCCTCCA	19165
rs580093070	snp	A/T			intron-variant	Psen2	GRCm38.p3	1:180243635	CCACTGCACACTGTG[A/T]TTGTGTAGCCCACTG	19165
rs580202488	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180243949	GACTGTGTAGCCCAC[C/T]GCACACTGGGACTGT	19165
rs580493704	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180243925	TTTGTGTAGTCCACT[G/T]TACACTGTGACTGTG	19165
rs580622260	snp	C/T			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180260517	TAGAATGTATACATA[C/T]ATAAACATACATATA	19165
rs580651500	snp	C/G			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263125	AGTCTCTCTCTCTCT[C/G]TCTCTCTGTCTCTCT	19165
rs580654890	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180240158	CCCATGGGGCAGGGG[G/T]GGGGTGGGGTGGGGG	19165
rs580708670	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180241585	CAGCACATGGTTACC[C/T]CATCTGGCTACCTAC	19165
rs580815173	snp	C/G			intron-variant	Psen2	GRCm38.p3	1:180243738	CTGTACACTGTGACT[C/G]TGTAGCCCACCACAT	19165
rs581044645	snp	A/T			intron-variant	Psen2	GRCm38.p3	1:180243685	CCACTGCACACTGTG[A/T]TTGTGTAGTCCACTT	19165
rs581063594	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180244000	ACTGTGTAGCCCACC[A/G]CATACTGTGACTGTG	19165
rs581188526	snp	A/C			intron-variant	Psen2	GRCm38.p3	1:180236348	CAGAGGCAGAGGCAT[A/C]TCTGAGTTTGAGGCC	19165
rs581188797	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180249365	CACACACACACAGGA[C/T]TTGGAAAACTATTAC	19165
rs581212208	snp	A/C			intron-variant	Psen2	GRCm38.p3	1:180249317	AAATGTTCTTATAAA[A/C]ATCTGAATTTCACAC	19165
rs581272880	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180234935	AGCACTTGAGACACC[A/G]CTCCATCAATGAGCC	19165
rs581305545	snp	A/T			intron-variant	Psen2	GRCm38.p3	1:180243785	CCACTGCACACTGTG[A/T]CTGTGTAGCCCACTG	19165
rs581325336	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244511	CACCGCACACTGTGA[C/T]TGTGTAGCCCACCGC	19165
rs581473096	snp	C/G			intron-variant	Psen2	GRCm38.p3	1:180253243	AGACACACACACACA[C/G]ACACACACACACACA	19165
rs581605926	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244024	GACTGTGTAGCCCAC[C/T]GCACACTGTGACTGT	19165
rs581736382	snp	C/G			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263197	TCTCTCTGTCTCTGT[C/G]TCTCTCTCTCTCTCT	19165
rs581749036	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180241826	ACTGTGTAGCCCACC[A/G]TACACTGTGATTGCG	19165
rs581755059	snp	C/G			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263175	TCTCTGTCTCTCTGT[C/G]TCTCTGTCTCTCTGT	19165
rs581872465	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180242162	CACTGCACATGGTGA[C/T]TGTGTAGCCCACTGC	19165
rs581969000	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180244531	TAGCCCACCGCACAC[G/T]GTGACTGTGTAGCCC	19165
rs581986057	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180243851	CTGTGTAGCCCACTG[C/T]ACACTGTGACTGTGT	19165
rs581997529	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180243878	GTGTAGCCCACTGCA[C/T]ACTGTGACTGTGTAG	19165
rs582148864	snp	C/G			intron-variant	Psen2	GRCm38.p3	1:180253277	ACACACACACACAGA[C/G]ACACACAGACACACA	19165
rs582174774	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180239560	TGAGTGCATCTACTC[C/T]ATTGCTGCTGCTGCT	19165
rs582381092	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180241862	CACTGCACACTGTGA[C/T]TGTGTAGCCCACTGC	19165
rs582444075	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180243926	TTGTGTAGTCCACTG[C/T]ACACTGTGACTGTGT	19165
rs582527264	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180237508	GAAGGAAGGGACGGC[A/G]TGGCCTTTATAACCT	19165
rs582538625	snp	C/G			intron-variant	Psen2	GRCm38.p3	1:180253229	AGACACACACACACA[C/G]ACACACACACACAGA	19165
rs582558699	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244630	GTAGCCCACTGCACA[C/T]TGTGACTGTGTAGCC	19165
rs582559428	snp	C/G			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263185	TCTGTCTCTCTGTCT[C/G]TCTGTCTCTGTCTCT	19165
rs582566392	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180230451	AACCCCTCCACCCTT[C/T]CTTTAGAGCCCTGTC	19165
rs582570102	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244724	GACTGTGTAGCCCAC[C/T]GCACACTGTGACTGT	19165
rs582698113	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180228822	CCACGAGTGCCCACA[C/T]CCACCACACAGCCCA	19165
rs582862955	snp	A/C			upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180264897	GTGTGTGTATGCATG[A/C]GTGTGTGCGTGTGTG	19165
rs582932202	snp	A/C			intron-variant	Psen2	GRCm38.p3	1:180239583	CTGCTGCTGCCTCCA[A/C]CACCACCACCGCTGC	19165
rs583018530	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180243707	AGTCCACTTCACACT[A/G]TGACTGTGTAGCCCA	19165
rs583084289	snp	C/T			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263036	AGTGAAAATTTGCAC[C/T]CAGGAAGGAAGTAAA	19165
rs583115432	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180231725	ATCCCAGGGTCCTCA[A/G]GGCTCGCCCATATCA	19165
rs583214654	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180253317	ACAGTGTTATGGTTC[C/T]TTCTCTCCTCTCTCA	19165
rs583304697	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180243961	CACTGCACACTGGGA[C/T]TGTGTAGCCCACTGC	19165
rs583364283	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180243950	ACTGTGTAGCCCACT[A/G]CACACTGGGACTGTG	19165
rs583614168	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180243636	CACTGCACACTGTGA[C/T]TGTGTAGCCCACTGC	19165
rs583664661	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180240159	CCATGGGGCAGGGGT[G/T]GGGTGGGGTGGGGGT	19165
rs583669221	snp	A/G			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180260557	TATAGATAGATGGAT[A/G]GATGGATGGATAGAT	19165
rs583806314	snp	A/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180264868	TCATTAACTTTTTAC[A/T]TGCGTGAGTGTGTGT	19165
rs583854057	snp	A/T			intron-variant	Psen2	GRCm38.p3	1:180249327	ATAAACATCTGAATT[A/T]CACACACACACACAC	19165
rs583865045	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180234556	GTCCTTATAAGAGTT[A/G]CCTTGGTCGTGGTGT	19165
rs583926886	snp	A/T			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263216	CTCTCTCTCTCTCTC[A/T]CACACACACACAGAT	19165
rs584147850	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180241806	GTAGCCCACTGCACA[C/T]GGTGACTGTGTAGCC	19165
rs584371161	snp	C/T			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263131	TCTCTCTCTGTCTCT[C/T]TGTCTCTCTGTCTCT	19165
rs584377779	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180236558	TACTTCTGACAGTAC[A/G]TCAGAATGAAAGGGA	19165
rs584425589	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180244500	ACTGTGTAGCCCACC[A/G]CACACTGTGACTGTG	19165
rs584434588	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244549	GACTGTGTAGCCCAC[C/T]GTACACTGTGATTGT	19165
rs584486899	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244524	GACTGTGTAGCCCAC[C/T]GCACACTGTGACTGT	19165
rs584677244	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180243874	GACTGTGTAGCCCAC[C/T]GCACACTGTGACTGT	19165
rs584715511	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180243786	CACTGCACACTGTGA[C/T]TGTGTAGCCCACTGC	19165
rs585059351	snp	C/G			intron-variant	Psen2	GRCm38.p3	1:180235289	GTTGCTTGACGCACA[C/G]CACACACACACACAC	19165
rs585135949	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180243751	CTGTGTAGCCCACCA[C/T]ATACTGTGATTGTGT	19165
rs585197572	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180244457	AGCCCACTGCACACT[A/G]TGACTGTGTAGCCCA	19165
rs585317631	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180241827	CTGTGTAGCCCACCA[C/T]ACACTGTGATTGCGT	19165
rs585321558	snp	C/T			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263179	TGTCTCTCTGTCTCT[C/T]TGTCTCTCTGTCTCT	19165
rs585403994	snp	C/G			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263189	TCTCTCTGTCTCTCT[C/G]TCTCTGTCTCTCTCT	19165
rs585463303	snp	A/T			intron-variant	Psen2	GRCm38.p3	1:180239572	CTCCATTGCTGCTGC[A/T]GCTGCCTCCACCACC	19165
rs585519662	snp	A/T			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263212	CTCTCTCTCTCTCTC[A/T]CTCTCACACACACAC	19165
rs585574127	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180242196	TGGTGACTGTGTAGC[C/T]CACTGCACATGGTGA	19165
rs585757396	snp	C/G			intron-variant	Psen2	GRCm38.p3	1:180253285	ACACAGACACACACA[C/G]ACACACAGACACACA	19165
rs585774278	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180243932	AGTCCACTGTACACT[A/G]TGACTGTGTAGCCCA	19165
rs585849136	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180230687	GTAACCATAGGGGTT[A/G]GAGAGAGGGCTGTGG	19165
rs585859292	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180244725	ACTGTGTAGCCCACT[A/G]CACACTGTGACTGTG	19165
rs586011099	snp	A/C			intron-variant	Psen2	GRCm38.p3	1:180230353	GCCTCCAAGTAAGAA[A/C]TAATCTTTGTCGTCT	19165
rs586262445	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180237635	TGTTGGGACTGGCCC[C/T]ATGACATGTACTGAC	19165
rs586326790	snp	A/C			intron-variant	Psen2	GRCm38.p3	1:180239658	ACTAAAGGCCAGCAG[A/C]TCTCTTGGAACCTTG	19165
rs586363923	snp	A/T			intron-variant	Psen2	GRCm38.p3	1:180243885	CCACTGCACACTGTG[A/T]CTGTGTAGCCCACTG	19165
rs586390565	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180243594	CCTGTGATTGTGTAG[C/T]CCACTGCACACGGTG	19165
rs586398330	snp	A/C			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263340	GAAATTGACAAGTCG[A/C]TTATAAATGTTTAAA	19165
rs586403278	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180229054	AAAAAAAAAAAAAAA[A/G]AGAAAAAAAAAAAGG	19165
rs586479483	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180237500	CAGCCTGAGAAGGAA[A/G]GGACGGCGTGGCCTT	19165
rs586527713	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180264894	TGTGTGTGTGTATGC[A/G]TGCGTGTGTGCGTGT	19165
rs586555553	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180241116	CTTAGAAGACGGTGG[C/T]GGTGGAGGAGGGTCA	19165
rs586681443	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180243732	AGCCCACTGTACACT[A/G]TGACTGTGTAGCCCA	19165
rs586725516	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180232126	CAAAAGGCAATATGT[C/T]TTCCTTGTTCCTCGG	19165
rs586890714	snp	C/G			intron-variant	Psen2	GRCm38.p3	1:180236345	AGGCAGAGGCAGAGG[C/G]ATCTCTGAGTTTGAG	19165
rs586894629	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180249363	CACACACACACACAG[A/G]ACTTGGAAAACTATT	19165
rs586906170	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180243661	CACTGCACACTGTGA[C/T]TGTGTAGCCCACTGC	19165
rs586954552	snp	C/G			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263123	ACAGTCTCTCTCTCT[C/G]TGTCTCTCTGTCTCT	19165
rs587089530	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180243953	GTGTAGCCCACTGCA[C/T]ACTGGGACTGTGTAG	19165
rs587132079	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180240165	GGCAGGGGTGGGGTG[G/T]GGTGGGGGTGGGGAG	19165
rs587136091	snp	A/C			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180261982	GCCTAAGGCAAATGG[A/C]CCTTCTCCTCTCCTA	19165
rs587144583	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180234565	AGAGTTGCCTTGGTC[A/G]TGGTGTCTGTTCACA	19165
rs587177495	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244636	CACTGCACACTGTGA[C/T]TGTGTAGCCCACTGC	19165
rs587466562	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180247980	CCACGGCCCCACATC[A/G]AAGTTATCCTTAAGC	19165
rs587558381	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180243753	GTGTAGCCCACCACA[C/T]ACTGTGATTGTGTAG	19165
rs864309366	snp	A/T			missense, nc-transcript-variant	Psen2	GRCm38.p3	1:180238943	ACGCTGATCATGATG[A/T]GGGTGTTAAGCACGG	19165

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