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 |