SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4229465 | snp | C/T | 0.287335 | 0.247197 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84918795 | TTGGCCGTTTGGGGC[C/T]GTTCTTCCTCCTAGG | 68497 |
rs4229466 | snp | A/G | 0.21875 | 0.248039 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84918724 | AGGGGGTCAGTGTGT[A/G]TGTGTGACTAGACCT | 68497 |
rs4229467 | snp | C/G | 0.21875 | 0.248039 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84918689 | TTTTAAGCTCTAGTC[C/G]TAGCACTTTTTCAGA | 68497 |
rs4229468 | snp | C/T | 0.21875 | 0.248039 | utr-variant-3-prime, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84918559 | GGTTTTCTATTCTTC[C/T]AGTTCACTCTCCTGA | 68497 |
rs13467237 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84920064 | GACCAGACTGGGTAA[A/G]GCATCACCTCTTCTC | 68497 |
rs13467238 | snp | G/T | 0.231111 | 0.249285 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84919850 | GATCATTAATCTATA[G/T]GGAATTTGCTAAGCT | 68497 |
rs13467239 | snp | A/C | 0.231111 | 0.249285 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84919915 | TACAAAAGGATGTCT[A/C]TAAGGTGACAGAACT | 68497 |
rs13467240 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84920135 | TTCTGTTGGAAAGCC[C/T]GCATGTGAGACCCTT | 68497 |
rs13467241 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84920056 | TGGGTAATGCATCAC[A/G]TCTTCTCATCAGTGG | 68497 |
rs13467242 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84919739 | CGCTTCTCTCGTGGG[C/G]AAGGGCCGTGTCCAG | 68497 |
rs13481567 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Arel1 | GRCm38.p3 | 12:84923416 | TACTTGCTGCTCTAT[A/G]AATTTCAACATTGTA | 68497 |
rs45650444 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84967493 | AAATGTAAACATGTA[C/G]TTTGAGACTAGAAAT | 68497 |
rs45654899 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84935599 | GCCATTGGAATGTGC[C/T]CACACTCATACACAC | 68497 |
rs45661481 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84949648 | ACAGTCTATTAGCTC[A/G]GTGTGGAGATCAGGT | 68497 |
rs45681659 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84922840 | GACTCTCTTGTTCTC[A/G]ACTCCTAAGGCCTTT | 68497 |
rs45690552 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84918860 | GCTGAGAGGCAGCAG[A/G]GTAGTGGCTAAATGA | 68497 |
rs45707446 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84936071 | CCCAGAGTCCTGTCC[C/T]TGTGCACGGGTGAGG | 68497 |
rs45714058 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84960343 | TCGTGTGCACATAGC[C/T]GAACATGCATAAATA | 68497 |
rs45760068 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84939387 | GATACTACTTCTCTT[A/C]TTTGGAAAGAACACA | 68497 |
rs45780212 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84944203 | TGTGCGTCAAGGTTT[G/T]AAGAGAGAGAGAGGT | 68497 |
rs45829377 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84955976 | ATTCAGCTGAGACAA[G/T]GTCCTTAGCGTAGAA | 68497 |
rs45841138 | snp | C/T | 0.152778 | 0.230321 | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947674 | TCTACTTTCTGTTGG[C/T]CCCACTTTCATACAA | 68497 |
rs45864042 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Arel1 | Mm_Celera | 12:84924486 | TGGCAGAAGCATCTG[C/T]TCCCACACATTCCTC | 68497 |
rs45867054 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84958337 | AAAGAAAGCTGAGAA[C/T]GGAAATCCCAGACCC | 68497 |
rs45907252 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Arel1 | Mm_Celera | 12:84939116 | TATCTGGCACAAAGG[A/C]AGGAATCACACATGG | 68497 |
rs45988810 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Arel1 | Mm_Celera | 12:84924177 | TGTGGTAAAACTGTA[C/T]GCTGTATCAGCCTGA | 68497 |
rs46004732 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969368 | GGTGTCTGGGTAATA[C/T]AGGTGCTGTGATGAT | 68497 |
rs46082628 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971045 | CAGATATAGACTCGG[C/T]GCTTCCTTGTTTGTT | 68497 |
rs46165476 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84956821 | AAAGCTAAAACATGG[A/G]CATGTTCAAACAGTC | 68497 |
rs46184860 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84918639 | AACCTGGCATGCTAG[C/T]TGCCCCAGCTGGGCT | 68497 |
rs46221596 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Arel1 | Mm_Celera | 12:84924895 | TCTGTTGAGAATCTT[A/G]CAGGTGAATAACCTG | 68497 |
rs46222386 | snp | C/G | 0.231111 | 0.249285 | downstream-variant-500B | Arel1 | Mm_Celera | 12:84918043 | ACTCTGTTCACAGCA[C/G]ATTGCTTCCTGCTTC | 68497 |
rs46279685 | snp | A/G | 0.277778 | 0.248452 | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947149 | TAGATAGAAACTATA[A/G]TAAATATGAATAAAG | 68497 |
rs46282918 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947576 | AATGTATTCATTAAG[C/T]TCTTTAAGGCCCAAA | 68497 |
rs46380964 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84918293 | CTTGGTACTCATGAC[C/T]GGTCTCCTTCAAGGA | 68497 |
rs46395927 | snp | C/T | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84960498 | ATTCAGACCTAACCC[C/T]GACTCTAATTGGAAT | 68497 |
rs46473294 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84941588 | AAGCCTCTCCAGATA[A/T]TAATAATTCCCAAGT | 68497 |
rs46535343 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84940356 | AACCCGCAGTCCCAC[A/G]GGCCGATGTGCAGGG | 68497 |
rs46670485 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84924998 | TACAAAGACAGAAAA[C/T]GGGCATTCCTAGCCT | 68497 |
rs46681976 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84924554 | AGACTTGGGAAGTTG[A/G]CATCAGACACTGCAG | 68497 |
rs46691549 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84961722 | CTGATGGAACCCAAC[A/G]TTTACTTTTATAGTT | 68497 |
rs46700332 | snp | A/G | 0.375 | 0.216506 | intron-variant | Arel1 | Mm_Celera | 12:84932985 | TGTTATGTAAATGTT[A/G]TCATACACAGTTCCT | 68497 |
rs46713480 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84934555 | AAAAAGACCAAGTCA[C/T]AGCTTTCAACTCACC | 68497 |
rs46718782 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Arel1 | Mm_Celera | 12:84962532 | CCTAAGCAAGTCCAC[A/G]TCCCTTAAGTCTCTT | 68497 |
rs46746979 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84944256 | GACAGGAAAGTGCCT[A/G]CCTGCCTCTGACAAT | 68497 |
rs46749175 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84937400 | TTCAAACACTCTTCA[A/T]ATGACTTAGTGGAGA | 68497 |
rs46755709 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84959219 | ACAGCACCAACTCTG[A/G]GGAGAGGTCATATGC | 68497 |
rs46755958 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84955160 | CTTCCCATTCTACTA[A/T]ACCTCTTCTAAAAAC | 68497 |
rs46791886 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84949004 | AAAGCTAAAATCAGG[A/G]CTACAAATTCCTCCA | 68497 |
rs46815474 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948160 | CCAAAAGATAAGCAC[C/T]ATTATTCTCACAGGT | 68497 |
rs46838977 | snp | C/T | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84921991 | CTAGTCAGCAGAGGA[C/T]TGCCCAGGGGAAGGG | 68497 |
rs46866198 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84952454 | ACACAAAATGCTAAA[C/T]AAACCAGAACAGAAG | 68497 |
rs46889211 | snp | C/T | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84924213 | TCTACAGGCAGTGAC[C/T]GGACTCCCTCAAGTT | 68497 |
rs46892225 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84919512 | CCTTGTCTGTCCCCA[A/G]TGGCTTCACCGCTCC | 68497 |
rs46893973 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84950100 | TTCATCTCTCTCTGT[C/T]CACTCATGTGGATCT | 68497 |
rs46926252 | snp | A/G | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84967405 | GTTACTCCATTTAAA[A/G]TCACCAGGTTAGATT | 68497 |
rs46964661 | snp | A/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971435 | TTTTGTTTTGCTTAT[A/T]ATGTCTTAGGTCTGT | 68497 |
rs46971672 | snp | A/G | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84966151 | CTGGCCAGAAAGTAC[A/G]ATGAGCACAAAATGC | 68497 |
rs46977075 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84954851 | TACAGGGAACCCTTA[A/G]TGCTGCTGGCATCAG | 68497 |
rs46978710 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Arel1 | Mm_Celera | 12:84952352 | TTTCCCAGTTAACTC[A/C]CAAAAGCAGCAGACA | 68497 |
rs47001244 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84922065 | GCTGAACTTTTAACT[A/G]CTTCCCTTTAGCTCT | 68497 |
rs47001891 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84945377 | TGGCACACAGCCTCG[A/G]TGACTGTCATGGGTT | 68497 |
rs47016525 | snp | G/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947768 | ACAACTTACTTCCAA[G/T]TTAGCTGACATTCCT | 68497 |
rs47029615 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84931437 | CAGCACACCGGAGAC[C/T]ATGAACAGGCACAGA | 68497 |
rs47035108 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84919572 | CACAGCTGGCAGGCT[A/C]TGTCCCAGTCTGTTG | 68497 |
rs47065178 | snp | C/T | 0.244898 | 0.249948 | missense, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84927330 | TGTCAGTGAACCGGG[C/T]GAAGAGCTGACTGGT | 68497 |
rs47080019 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84923945 | GTATCCAAGTTAGAG[A/C]CAGACTGCTACTATG | 68497 |
rs47080340 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84930975 | TATAGTCTCAGGAGA[C/T]GGTTCTGCCTTGCTG | 68497 |
rs47092456 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84943486 | AGCCTACCAGCTCTA[A/G]TCTCGTGCCTTAACG | 68497 |
rs47097458 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Arel1 | Mm_Celera | 12:84952235 | CAGCACAGACTATTA[C/T]CAGCCTTCAGGATTT | 68497 |
rs47111728 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84956704 | ACAGATGACGTGTTC[C/T]TGCAATATCTCTCTT | 68497 |
rs47221476 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B | Arel1 | Mm_Celera | 12:84918063 | CTTCCTGCTTCCAAG[A/G]ACACATAAAGCATCT | 68497 |
rs47299548 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84924653 | GCCACCGAGGGGCAT[A/G]TGAAGAAGTCCCAAA | 68497 |
rs47360836 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969169 | TAGAGACCTGAAAGT[C/T]TAGTAAGAGTTCTGA | 68497 |
rs47367496 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Arel1 | Mm_Celera | 12:84961462 | GGCTTGCCTCTTGAG[A/T]TCTTGTTTTTAAACT | 68497 |
rs47375800 | snp | A/C | 0.5 | 0 | intron-variant | Arel1 | Mm_Celera | 12:84925594 | TCAGCGTCACTCAGT[A/C]CTCTGCAGAGTCTTT | 68497 |
rs47396440 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84967719 | AGAAGGACTAAAGTA[A/G]TTCTTTCCCTCACGA | 68497 |
rs47400190 | snp | C/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947207 | TCTGTTCTTTTCTTA[C/G]CTCAGATGCCTAAAG | 68497 |
rs47400230 | snp | C/T | 0.32 | 0.24 | utr-variant-5-prime, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84951363 | TGAAAGAGGCATCTG[C/T]TCTGGAACCAGGATC | 68497 |
rs47416294 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84961411 | TCTTCTTCCTACTGA[A/G]CTCTAGGTCTTTATA | 68497 |
rs47416950 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84943567 | CAAATAGACTATGGC[A/G]CTCTGCCTAAGGGCT | 68497 |
rs47419561 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84931980 | ACACGCCGTCCCAAT[C/G]CTCTAGTCTGACAGT | 68497 |
rs47433953 | snp | A/C | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84961434 | TCTTTATAGACTCTA[A/C]ATGGAAGCCCTTGGC | 68497 |
rs47465940 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84957566 | TCCTGCTGAATCCCC[A/G]CTTCTTCCTAGCAAG | 68497 |
rs47496978 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84922764 | TTTCTAACAGGAACG[A/T]TATGAAGAACTTTGA | 68497 |
rs47501314 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84945185 | CTCGTCTTAGAACAT[C/T]TGAGTAAGGCCTGAG | 68497 |
rs47505475 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Arel1 | Mm_Celera | 12:84931939 | GGTGAAGGTCAATCC[C/T]GACCTGACACCGTGA | 68497 |
rs47509337 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84944193 | TATATCTGATTGTGC[G/T]TCAAGGTTTTAAGAG | 68497 |
rs47510631 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84940721 | CAGCTCTATTCTAGC[A/C]TCAGTGCTAACCCAA | 68497 |
rs47519110 | snp | G/T | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84918150 | ACTCATTTAGCTCTT[G/T]ATTATTGTAGGCATT | 68497 |
rs47527710 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948131 | CACATCTTACCCTAC[A/G]AACCTAACTGTGACC | 68497 |
rs47528088 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84940153 | AAGGAATGAACCACG[A/G]ACCTACCAGGCTGAA | 68497 |
rs47530187 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Arel1 | Mm_Celera | 12:84924473 | ATGCTCTTTCATATG[A/G]CAGAAGCATCTGCTC | 68497 |
rs47566634 | snp | A/C/G | 0.132653 | 0.220748 | intron-variant | Arel1 | GRCm38.p3 | 12:84945376 | CTGGCACACAGCCTC[A/C/G]ATGACTGTCATGGGT | 68497 |
rs47566976 | snp | G/T | 0.244898 | 0.249948 | synonymous-codon, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84935101 | ATGGCACACAATTTT[G/T]GTTTTGGAAGGAACC | 68497 |
rs47573719 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84937419 | ACTTAGTGGAGAACT[A/G]TGGTTTGGGGCTTTG | 68497 |
rs47591557 | snp | C/T | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84923975 | GGCCCCAACGTGTGA[C/T]GCACAAGGAGACGGG | 68497 |
rs47605539 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84943829 | GTCATGCTAGCATCA[A/T]GAAAGCAAAGTGAAC | 68497 |
rs47612852 | snp | A/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84970552 | ATGTGCCAGAGGAAA[A/T]CCAGAATGTACTGTC | 68497 |
rs47633677 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84941150 | GTGGGCTTTCCGGCT[A/C]CATTTACTATACTAA | 68497 |
rs47664824 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84935208 | TGTTGCTTTGAGAAA[C/T]GGCTTTGTTTTTCTT | 68497 |
rs47670626 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948882 | CTGAACCATGAAAAA[A/G]AATGAAGTAATAGAA | 68497 |
rs47692430 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84938817 | AGGCATTCAGGCAAA[C/T]GAGACTGATAATGCA | 68497 |
rs47740967 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84934074 | CCCAGGCTGTCACTT[C/T]AGAGTTTCCATTACT | 68497 |
rs47751117 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84956664 | CTGGGCACTGGGGCA[A/T]GCAGAAGACGCCAAA | 68497 |
rs47764556 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84927646 | GATCCAGGAAATGGA[C/T]ACTGTGGTTCTGCAG | 68497 |
rs47771059 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84952341 | GAGTAAGATACTTTC[C/T]CAGTTAACTCCCAAA | 68497 |
rs47781974 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84950990 | TACTGTTCTCCAGCC[A/G]ATAGACATTGTGGAA | 68497 |
rs47872561 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969573 | GTCAGTGTCATGCAG[C/T]AAGAAAATCACAAGC | 68497 |
rs47897920 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84933708 | ATAGGATTTCCAGTA[A/G]TCTCATTTTTGTGAG | 68497 |
rs47900331 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969472 | GAGAGGGAGTGAACT[A/G]CAGCCAGTCAAACGC | 68497 |
rs48009942 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84960266 | GGCTGCAGAGATGGC[A/G]CTGCCATGTCAGTTG | 68497 |
rs48030889 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84963682 | ATGAGGAAGTGAATG[A/G]AGTCAGGGAACACTG | 68497 |
rs48041802 | snp | G/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971589 | GGGAAAAGTCCAAGA[G/T]AGTCCCATTTTATAA | 68497 |
rs48090054 | snp | C/T | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84920961 | TGCTCCCAGTTACAG[C/T]ACTATGAGGCATGAA | 68497 |
rs48112355 | snp | A/G | 0.46281 | 0.131194 | synonymous-codon, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84930392 | AGTGGCTGCTAGGAT[A/G]TTCCTTTCTTTACAG | 68497 |
rs48159456 | snp | C/T | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84962339 | AGAACCCAGAACACG[C/T]TCCTTGGGACAAAGC | 68497 |
rs48167189 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Arel1 | Mm_Celera | 12:84934064 | CCTACTGACACCCAG[A/G]CTGTCACTTCAGAGT | 68497 |
rs48285998 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Arel1 | Mm_Celera | 12:84931691 | GCTCAGCACAAGGTC[C/T]GCCTTACCTTTGTTC | 68497 |
rs48303875 | snp | A/G | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84930151 | TCTGCTGACCTTCAG[A/G]GTGACTTTGGAATGA | 68497 |
rs48320241 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84946238 | ACTATTTTAGTTTCC[A/G]TTCATGGAATAACTC | 68497 |
rs48331573 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84919523 | CCCAGTGGCTTCACC[A/G]CTCCTTTGCCTTAGC | 68497 |
rs48344817 | snp | A/C | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972227 | CAATGTCCCACTGAT[A/C]ACTTCCTTGTGTTGA | 68497 |
rs48361660 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Arel1 | Mm_Celera | 12:84949865 | AGAAAGGCCCCTCTA[C/T]ATTGACTGGAGTGAG | 68497 |
rs48378925 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84923660 | TGAGGCACACCCTCA[A/C]GAACGCAGCAGTCTT | 68497 |
rs48395501 | snp | C/G | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84949685 | CTGTCCCAAGTTACT[C/G]TGTTGTATAACAAAG | 68497 |
rs48396275 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Arel1 | Mm_Celera | 12:84923838 | ACCACAAACAAGATA[A/G]GTTCAAATCCTAAGC | 68497 |
rs48397372 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Arel1 | Mm_Celera | 12:84929890 | AGCACCGACCAGAGA[C/G]CTGATGTCTGTCAGT | 68497 |
rs48404893 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84919559 | CAAAGATCACCACCA[C/T]AGCTGGCAGGCTCTG | 68497 |
rs48404972 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Arel1 | Mm_Celera | 12:84966934 | TTTTTCCAAGTTGAC[C/T]ACTTGGTATAGTATT | 68497 |
rs48436944 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84956598 | CCCCAAATCACAGAA[A/C]GCTGGTGTGCTGCCG | 68497 |
rs48466747 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Arel1 | Mm_Celera | 12:84923101 | AAATGTGAAATCACC[A/G]TTACTTAGATATGTA | 68497 |
rs48477600 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972121 | AAGACTGGGCTTCTT[C/T]GTGTTTAAGATTTTC | 68497 |
rs48509622 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84918360 | CCCAAGTACCTATGT[C/T]ACAAAGCACAAACAA | 68497 |
rs48562577 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Arel1 | Mm_Celera | 12:84922863 | AGGCCTTTCATTCAG[C/T]TGACCATAAAAATGG | 68497 |
rs48578409 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84959195 | GAAACCTAGACTTGG[A/G]AGAGAATGACAGCAC | 68497 |
rs48598468 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84922236 | TTGGCTCAAGAGCCA[A/G]CATGTTACTTAGCAG | 68497 |
rs48601625 | snp | A/C | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84945257 | ATCCTTTCCTCTAAC[A/C]TCACAGCCCTAGAGG | 68497 |
rs48610312 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84962651 | CATTCCACTTCAGTC[G/T]GGACCAGTGCACTAA | 68497 |
rs48644189 | snp | A/C | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969485 | CTGCAGCCAGTCAAA[A/C]GCCCGAGTCCCATAA | 68497 |
rs48700930 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Arel1 | Mm_Celera | 12:84925211 | GCAGAGGCACTATCA[A/G]AGCTAATGAAGTTTA | 68497 |
rs48703917 | snp | A/T | 0.396694 | 0.202437 | intron-variant | Arel1 | Mm_Celera | 12:84944903 | CATTAAAGCAAACCA[A/T]CCAACAAATTCTAAG | 68497 |
rs48705348 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84934866 | AGGCACTACCAGATA[C/T]AGCCAAGGAGGCTCA | 68497 |
rs48708048 | snp | C/T | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84958985 | GTCATGGTGGCAGTG[C/T]CAGCTGTCCCTGCAA | 68497 |
rs48710338 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948861 | TTCAACTTTGTACCC[A/G]TAATTCTGAACCATG | 68497 |
rs48756574 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969350 | ACACAGGTCGGTCCT[A/G]GTGGTGTCTGGGTAA | 68497 |
rs48767808 | snp | A/C | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84957344 | TCCTATCATAGAGAT[A/C]ATCTGGATACTACAC | 68497 |
rs48807561 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84944402 | ACAAGTTAGGATTTA[C/T]TATCTTCACCTCCTT | 68497 |
rs48827872 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84957392 | CTACCTCCCTGCCTT[C/T]GGTTTTTTTCTCAAG | 68497 |
rs48834815 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Arel1 | Mm_Celera | 12:84941614 | CAAGTTCCTGGGAGG[A/G]ACTGAAAACAAGGGA | 68497 |
rs48845248 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84945224 | CTTGCAAACTCACTG[G/T]TCTGACCTTTCTAAA | 68497 |
rs48847619 | snp | G/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969611 | ACTGACCTCTGAGCG[G/T]CTAGGGCACAGCTTC | 68497 |
rs48868346 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84944411 | GATTTACTATCTTCA[C/T]CTCCTTAGCATAACT | 68497 |
rs48897436 | snp | C/G | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84955115 | CCTGGTTTTGAGACA[C/G]GGCCTCTCTACATAG | 68497 |
rs48989210 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84950697 | ACTGAATCTATTCAA[A/C]CCAATTTACCCCTCT | 68497 |
rs49023244 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84924754 | ATTAGTTGTGAGGTC[A/G]GTTATTTTAAGGACC | 68497 |
rs49042514 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84920216 | CACAGAGATCTTCAA[A/G]GGACCAACGAAGTGA | 68497 |
rs49055498 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84929177 | TCTAAGCATGGTAGG[A/G]AATCCCCATGACCAC | 68497 |
rs49128668 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84965537 | GGAGAGCAAGCTCTA[A/G]GCAGCAAGAACCACA | 68497 |
rs49147678 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84920410 | GGTTAAGGTCAGTGG[C/T]TATGCTTGTTAACAT | 68497 |
rs49164105 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84940698 | AAATGCTGCCTCCTC[A/G]GTGTCCCCAGCTCTA | 68497 |
rs49164140 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84944912 | AAACCATCCAACAAA[G/T]TCTAAGTGCTTGCTG | 68497 |
rs49169713 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84962507 | CTAATGAAGCTTAAG[A/G]TGACCAGAACCTAAG | 68497 |
rs49188437 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84957326 | CTAGATGCTTACACA[A/T]GGTCCTATCATAGAG | 68497 |
rs49202083 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84944360 | CTAATCTACACCTCC[A/G]TGGGTGTGACAGTTC | 68497 |
rs49214443 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84935548 | GGAGAGAAAGACATT[C/T]CACAAAGCTGCTCTC | 68497 |
rs49228582 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84919238 | TTCTGAGTGAGTGCC[C/T]CATGGAAAATAGTGG | 68497 |
rs49239004 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84964244 | TTTATTTCTCTTGGC[G/T]TCTTCTTTTATTTTT | 68497 |
rs49264940 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84943214 | AACTGTGTGAGGGTA[C/T]GTTCTGGCACAAGTG | 68497 |
rs49287246 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84940805 | TCATACACCAAACTT[C/T]GTCCTACCTCGTGGA | 68497 |
rs49293846 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84952505 | AATAAGTTGGCAGAC[A/T]TTTATAATTAAAAAT | 68497 |
rs49295651 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84951642 | CTCACGCTCCTCAAA[C/T]GCCCCAGGCTTTCAG | 68497 |
rs49304099 | snp | C/T | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84921922 | TAAGAACTGCTAAGG[C/T]GGCTTTGTCATTACA | 68497 |
rs49320126 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84933980 | AGCGGTGGGGACCTC[C/T]AGTTCCATGCATGCT | 68497 |
rs49363556 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84967783 | ATTCAACACAGTCAA[A/G]ACCATGCTACCTTCC | 68497 |
rs49385055 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969636 | AGCTTCAACATCGGT[A/G]AAACAAAGGTATCAA | 68497 |
rs49471674 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84950077 | ACTGCTGCCTGTCTC[A/G]CCATTTCTTCATCTC | 68497 |
rs49473107 | snp | G/T | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84934374 | TGAGGTGGACACATT[G/T]CGTTCAACAATATTC | 68497 |
rs49489549 | snp | A/G | 0.231111 | 0.249285 | utr-variant-5-prime, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84970960 | CAGGAGTGCGGCGTG[A/G]ACATGGTGAGCGGAG | 68497 |
rs49500709 | snp | A/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948920 | AGTATTTAGAGAAAA[A/G]GGATTTAAGAAAACA | 68497 |
rs49553426 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84943410 | GCAAAAGAACATCTG[C/T]TCAGTGTCTTCCAGG | 68497 |
rs49559973 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84952763 | GAAAAAGCAAGCTCA[A/T]CATTGTTCATATAGT | 68497 |
rs49560555 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84966496 | AATTAATGGCTAGAG[A/C]CATTTCAAAGGTAAA | 68497 |
rs49572842 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84967508 | GTTTGAGACTAGAAA[A/T]AATATCTCTACATTA | 68497 |
rs49709348 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84945435 | CCTACACTACTCTCC[A/G]TAGCCACACCTCACA | 68497 |
rs49728627 | snp | G/T | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84925576 | TTAGGCACGGATGCT[G/T]CATCAGCGTCACTCA | 68497 |
rs49780250 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84964079 | GGCTAAGGTTTGACC[C/T]GCTTGCTCCTTCCAG | 68497 |
rs49800045 | snp | C/T | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84940526 | ACCCGTGTCCACCTG[C/T]TCCTTTCAGTTTTCA | 68497 |
rs49817487 | snp | A/G | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972225 | AACAATGTCCCACTG[A/G]TCACTTCCTTGTGTT | 68497 |
rs49819271 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972137 | GTGTTTAAGATTTTC[A/G]GAACAAGAGAGTGGT | 68497 |
rs49823934 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84952760 | AATGAAAAAGCAAGC[A/T]CATCATTGTTCATAT | 68497 |
rs49864662 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Arel1 | Mm_Celera | 12:84958996 | AGTGCCAGCTGTCCC[A/T]GCAAGTCAGGAGGCT | 68497 |
rs49934155 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Arel1 | Mm_Celera | 12:84924369 | CTCAGGCAGTGAACG[A/G]TGCTGATGCAACAGG | 68497 |
rs49997184 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84921962 | GAAAGAAATAAAATA[A/G]CTGCGTCTGTGTTCT | 68497 |
rs50014817 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84963615 | CGTGTACAGGGCATG[A/G]AAGAAGCTGTATTCC | 68497 |
rs50044950 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84924382 | CGGTGCTGATGCAAC[A/G]GGAAGGTACTACGGT | 68497 |
rs50084407 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84941542 | CTTCCTCAAAGCTAT[C/G]TACCCAGTAAACCAA | 68497 |
rs50098281 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972557 | TAACAACCTCTTCAC[A/G]GCCTCTTACACGTGG | 68497 |
rs50113141 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Arel1 | Mm_Celera | 12:84924143 | GAAACAGAAGGCAAA[A/C]GACAAGACATGGAGA | 68497 |
rs50121265 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969885 | CATATTCTCCCTCTC[C/T]CATTAAGGACTGCAC | 68497 |
rs50217426 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84950190 | GGCTAATCCAGCTCT[G/T]ATCCTGCAGCCTAAC | 68497 |
rs50217925 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Arel1 | Mm_Celera | 12:84941995 | CCACATTACAGCGAC[G/T]ACAGAACAGACTGGC | 68497 |
rs50240702 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84939141 | ACATGGACAGATGCT[C/T]TTCGGGATGAAGTAA | 68497 |
rs50243317 | snp | A/T | 0.231111 | 0.249285 | utr-variant-5-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84951331 | TGGGCTCCTCTAGCG[A/T]AAGATGTAACCAATG | 68497 |
rs50254268 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84949739 | TTTTATCAGCAGCAA[C/T]TGACTCCAACTTGAG | 68497 |
rs50311585 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84921073 | TCCCACCCATTACCG[C/T]AGTGGTAGTCAAGGC | 68497 |
rs50337707 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84926733 | CATAAACGGAAGCCT[C/G]TAAAAGTCTGTGGTT | 68497 |
rs50349644 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84963225 | AAAACAATAATAGGA[A/G]CTTTTGGCTCTATTT | 68497 |
rs50354307 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84949510 | ATGAAGAATTAGTTC[A/T]AAACTGTTCTGCTAG | 68497 |
rs50361709 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947234 | AAAGTTCAAGAGTTT[C/T]GCAGAGGGAACAACC | 68497 |
rs50389109 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84966867 | TTGTAGGGTATGTTA[A/G]GCAGCCATACTCTAA | 68497 |
rs50465524 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84935673 | CAGTGAAAGCAAAAT[C/G]AAAGGGCGTGAGACA | 68497 |
rs50468279 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84943598 | TAGGGTCTACTGACC[A/G]TTCTCAGAAGGCAGC | 68497 |
rs50522881 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84941702 | ACTCAGAAACCATGA[C/T]GGGTATGGAGACAGA | 68497 |
rs50529356 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84934798 | CACTTTCTGCTTCAC[C/G]AAGAGCATCCCTGTG | 68497 |
rs50543030 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84951867 | TAAAGACTTTATGTC[C/T]GCCTAGGCATGCCAC | 68497 |
rs50558826 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84922414 | GCAGCTTTTCTCCCA[C/T]TCTCGGATGTGTTGT | 68497 |
rs50566481 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84954727 | ACTCAACCTAAGCAT[C/T]GCTACCCGTTTCCAG | 68497 |
rs50585495 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84918690 | CTGAAAAAGTGCTAC[A/G]ACTAGAGCTTAAAAT | 68497 |
rs50609383 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84949268 | ATCCAATACATTTTA[G/T]CCCCACTGCTGAAGA | 68497 |
rs50648115 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Arel1 | Mm_Celera | 12:84925674 | GGCTGTAGGGGCTTC[C/T]GAGTCCTGGTCTCTC | 68497 |
rs50652819 | snp | A/G | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84955180 | CTTCTAAAAACAAAA[A/G]CTAGAAAACTCAAAA | 68497 |
rs50660416 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84944821 | CAACAAATCTTACCC[G/T]TCAAGGGAATTCTTT | 68497 |
rs50675553 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84957565 | CTCCTGCTGAATCCC[C/T]GCTTCTTCCTAGCAA | 68497 |
rs50679606 | snp | A/T | 0.231111 | 0.249285 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84919114 | TCTCGTGATCCTGGG[A/T]ACAGGAGGGCTCAGA | 68497 |
rs50683245 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84941125 | ACCATGAAACAGAAA[C/G]TGGGCTGGCGTGGGC | 68497 |
rs50698223 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84962374 | AACAATCAGCCACAT[A/G]TCATTCTGGTGTGAC | 68497 |
rs50704590 | snp | A/G | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84927349 | GAGCTGACTGGTGGT[A/G]TCAAACAGTGCTTTG | 68497 |
rs50738895 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84957286 | CAAAGCCTTAAGCAT[G/T]CTATACTCCTATCAG | 68497 |
rs50784827 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84920040 | GCTGCACTTCTCCTG[A/G]CCACTGATGAGAAGA | 68497 |
rs50810535 | snp | A/C | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969238 | ACACATGAACACTCA[A/C]GTGGTGTAACCTTTC | 68497 |
rs50831762 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84949884 | GACTGGAGTGAGTTA[A/G]ACCACAGGAGCACAG | 68497 |
rs50914659 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84918313 | TCCTTCAAGGACACC[A/G]AAAAGCCAAAAGCCA | 68497 |
rs50963317 | snp | C/G | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84948966 | GAGAAGTCATCCAAC[C/G]TAATTATGAGGAATC | 68497 |
rs50963652 | snp | A/G | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84964055 | CAAACTCTCTCACTC[A/G]TTTTAACTGGCTAAG | 68497 |
rs50992447 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948217 | CCTAGAAAAGTTAAG[C/T]TGATGAGGCTCTCCT | 68497 |
rs51008848 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947574 | CCAATGTATTCATTA[A/G]GCTCTTTAAGGCCCA | 68497 |
rs51019952 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969934 | GAGCACTGTTCCCCA[C/T]CACATTCCAGGCTTG | 68497 |
rs51026503 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84956833 | TGGGCATGTTCAAAC[A/G]GTCATACACATTTTA | 68497 |
rs51071492 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84924410 | GGTCTCGTGAGCAAT[C/T]CTTTAATTCTTCTCC | 68497 |
rs51167451 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84950949 | TGGCAGACTGCCACC[A/C]TCAAAGCCAGTGTAC | 68497 |
rs51173007 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Arel1 | Mm_Celera | 12:84952281 | TTCTCTTTCTTAGGC[A/G]CAGATACAGGACTAC | 68497 |
rs51280693 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Arel1 | Mm_Celera | 12:84928014 | TCTAAAGAGAACCCT[C/G]AAGAGCAGCACTGCC | 68497 |
rs51303900 | snp | G/T | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84944092 | CCCGCACTCAGAGAC[G/T]AGACATCTAAAGATT | 68497 |
rs51395300 | snp | G/T | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84944063 | TTGTTTTCCCCCAAT[G/T]CGTACATCAGCATCC | 68497 |
rs51408592 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84952101 | GCTTCATAACACTCA[C/G]ACATTCAGGGACCAA | 68497 |
rs51416028 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84919824 | TTCTCACTGGCTCAA[A/G]TTCAAGAGAAAGCTT | 68497 |
rs51427866 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84952086 | TTACCAAGTAAAGTC[A/G]CTTCATAACACTCAC | 68497 |
rs51443429 | snp | A/C/G | 0.231111 | 0.249285 | intron-variant | Arel1 | GRCm38.p3 | 12:84954124 | AGTTGCTATTTCTGA[A/C/G]GAATATTAATTTTGG | 68497 |
rs51462079 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84924312 | CCACTATTCACACTC[C/G]ACTAGCTAAGACTTC | 68497 |
rs51524895 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84943905 | TTCGTGACATTACCA[A/G]ATCAGACAAACGGAT | 68497 |
rs51587503 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947072 | CCACAATGCACATTC[C/T]ATACACATACACAAC | 68497 |
rs51611260 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84963641 | ATTCCAGGAACTCTA[C/T]GTGTGTGGAAAAAAC | 68497 |
rs51725233 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84949074 | AAGCCAAAGCAGAGG[C/T]GGTGCCAGCTATCTA | 68497 |
rs51769195 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Arel1 | Mm_Celera | 12:84964547 | TCTGTGATCAGGTAG[C/T]CGTGGACTACTCGAG | 68497 |
rs51793759 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972080 | TCTCTGTATCGGTAA[A/G]GACTGGGTAAACAGT | 68497 |
rs51834223 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84939356 | CAAACACGGAGGCCG[A/G]AAAGACCACAAAAGC | 68497 |
rs51856827 | snp | A/T | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84918821 | GCCAAGCAGCCATGT[A/T]CCCAGCTGGAAGCCC | 68497 |
rs51917402 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84950227 | GTAGCAGTAGCCCCA[A/G]TGTCCAGCATGTTCA | 68497 |
rs51963744 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84963323 | ATGTGAGATCCCAAG[A/G]TAACCCTCCAGTACC | 68497 |
rs52005819 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Arel1 | Mm_Celera | 12:84949229 | CAAAATGATAACAGA[C/T]ATACACATTCTAAAC | 68497 |
rs52048985 | snp | A/G | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84952246 | ATTACCAGCCTTCAG[A/G]ATTTCCAGTGCATAT | 68497 |
rs52054945 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Arel1 | Mm_Celera | 12:84963533 | ATGCTGCTTTAGCTT[C/G]AATTCCTATAAAAGG | 68497 |
rs52059736 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Arel1 | Mm_Celera | 12:84944899 | CTCGCATTAAAGCAA[A/G]CCATCCAACAAATTC | 68497 |
rs52161077 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972317 | CCTCCTAAACTTGTG[A/G]TTTGAGTCCTTTTTG | 68497 |
rs52442849 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84922092 | CTCTGCTTCCAGTTG[A/C]ACAGATAAACTAAAA | 68497 |
rs52526445 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84946430 | GTAACTGATATGAGA[C/G]AAAAACTAATCTTAA | 68497 |
rs52594746 | snp | C/G | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84964700 | CAGCCCAGTGGGGTA[C/G]AAGTTTGCAATTCTC | 68497 |
rs52603928 | snp | A/C | 0.32 | 0.24 | intron-variant | Arel1 | Mm_Celera | 12:84966192 | AGCATTTTAACACTA[A/C]TATCAAAGTGCACCT | 68497 |
rs52626231 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Arel1 | Mm_Celera | 12:84929490 | GCAGTAAGCTGTAAA[C/T]AGAACTCATGAGTCT | 68497 |
rs52626874 | snp | A/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971813 | CTTCGAACATGCTAG[A/T]ATGATATTCCCATTA | 68497 |
rs52632506 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Arel1 | Mm_Celera | 12:84921490 | GCCAATGATTCCTAA[C/T]TAGTGTGGGATTTCA | 68497 |
rs52636153 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Arel1 | Mm_Celera | 12:84968187 | AAGTGCACAAGGATG[C/T]AGTCTGTCTGTCTCT | 68497 |
rs107711878 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84922449 | AATGCTCACACTACA[A/G]CAAAATACCCCAGGG | 68497 |
rs108000831 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84928866 | AAATTCAATTCCCAA[C/T]AACCACATGAAGGCT | 68497 |
rs108294465 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84922344 | GAAGCTTTAGTTTCT[C/T]GAAGACCATGCCAAG | 68497 |
rs211708173 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84965431 | TCTCTCTCATTCAGG[A/G]ATTACAGCCATTTGT | 68497 |
rs211740625 | in-del | -/TTGT | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971051 | AGACTCGGTGCTTCC[-/TTGT]TTGTTTGTTTGTTTG | 68497 |
rs211743193 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84922124 | GATGGGGGAGGGGGG[C/T]GCGGGGAAAGAGAGA | 68497 |
rs211809365 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84921549 | CACAGTATTAATAAA[C/T]CCACACCACTTACAC | 68497 |
rs211875785 | in-del | -/CA | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969552 | TCTGAACCCAGTAAC[-/CA]ACTAGGTCAGTGTCA | 68497 |
rs211960592 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84930071 | GATATAGTCAAATAC[A/G]GAAGAGCTTCTTAGC | 68497 |
rs211990420 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84938612 | CTGCCATATCACCAT[C/T]ACGCTACAATCTGAA | 68497 |
rs212015293 | in-del | -/TG | | | intron-variant | Arel1 | Mm_Celera | 12:84945499 | CCCAGGTCAGAAACT[-/TG]ACACTCGCATATATA | 68497 |
rs212016763 | in-del | -/G | | | intron-variant | Arel1 | Mm_Celera | 12:84940774 | ATTGGCACTGGGGGC[-/G]GGGGGCGACTCAGGG | 68497 |
rs212054039 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84939495 | CCCCCGACCTCCACA[A/T]GAGAACTGTGGCCTG | 68497 |
rs212057635 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947196 | ATTGTCAACTGTCTG[C/T]TCTTTTCTTACCTCA | 68497 |
rs212163135 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84931014 | CTCCAGGATGCCTGG[C/T]CCTTGAGCTTCCAAA | 68497 |
rs212211142 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84941189 | GGCTCCTCCCACCTT[C/T]CCTTTTACCCTTTTC | 68497 |
rs212257534 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84949335 | TTAGGGCTGGAGAGA[C/T]GGCTCAGTGGTTAAG | 68497 |
rs212323507 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948680 | AGGGCATGTTTACAA[A/G]ATACTGAGGCAGGAG | 68497 |
rs212330893 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84931663 | GAAGACTGAGCAGCC[C/G]AGAGCCGAGTCTGCT | 68497 |
rs212333694 | in-del | -/G | | | intron-variant | Arel1 | Mm_Celera | 12:84927779 | AGAAGCTGGGTCTTT[-/G]GGGGAGCTTGAAGAG | 68497 |
rs212382885 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84957869 | GAGGATCTGAGCTTG[A/G]TTCCCAGCACCCAGT | 68497 |
rs212405680 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84942593 | AGGGAGGAAGGAAGG[A/G]AGGAAGGAAGGAAGG | 68497 |
rs212446239 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84957082 | TTCAACATGGAATTT[A/T]CCAACAGCCAACACC | 68497 |
rs212500127 | in-del | -/G | | | intron-variant | Arel1 | Mm_Celera | 12:84923987 | GATGCACAAGGAGAC[-/G]GGGCCCACCTTTCAG | 68497 |
rs212537368 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84951242 | TGTGTCCCAGGAAGC[A/G]AAGAGTCAAGTGGTT | 68497 |
rs212539381 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84943368 | CTCTTCAACGCCACC[A/G]GACAGCCGAGGATCA | 68497 |
rs212540589 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961256 | GAGATCTGCTTGCTT[C/T]TGTCTTCCACATGCT | 68497 |
rs212606471 | snp | C/T | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969846 | CAAAACCAAACACTG[C/T]CCAGTTTCGCTTTCT | 68497 |
rs212722577 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84965951 | TCTTCCAAATAGCTT[G/T]ACCATTTACACCTGA | 68497 |
rs212777916 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Arel1 | Mm_Celera | 12:84924054 | CCGATACTGAGCCAG[C/T]AGGTTTAAATAGAAG | 68497 |
rs212842148 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84932248 | CTTGATGCCAAAGTG[A/G]CCTTGCTTCAGCTTC | 68497 |
rs212902015 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84923261 | TCTCTGGAATCTCAG[C/T]ACACAGCTCATAGTT | 68497 |
rs212932564 | snp | A/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972149 | TTCGGAACAAGAGAG[A/T]GGTCATTAGAACCTT | 68497 |
rs212988608 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84960540 | AAAATCACTGTACCT[A/C]ACTGAAATTTTAAAA | 68497 |
rs212995139 | snp | C/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971632 | CAGAACCTTGCCGGG[C/T]GGTGGTGGCACACGC | 68497 |
rs213046862 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84925542 | CTCCATCACAATGGC[C/T]AATCCCTCCCAGACC | 68497 |
rs213056409 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84968468 | TAATCTCCCACCCCC[A/C]AAAAACGGCTAAATG | 68497 |
rs213215485 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84944498 | AAACACAGAGGAGCA[A/G]GCAGACAGATGCCTC | 68497 |
rs213231041 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84956581 | CTTCTGAGTGGGCAA[-/T]CCCCCAAATCACAGA | 68497 |
rs213275073 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84943907 | CGTGACATTACCAGA[C/T]CAGACAAACGGATGG | 68497 |
rs213320770 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84962371 | GGAAACAATCAGCCA[C/T]ATATCATTCTGGTGT | 68497 |
rs213336473 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84960344 | CGTGTGCACATAGCC[A/G]AACATGCATAAATAA | 68497 |
rs213367893 | in-del | -/CTCAG | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948054 | AAAGGTTGGACTTGT[-/CTCAG]TGAATGAGGGCTGCT | 68497 |
rs213394593 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84959496 | ATCAGATGTCTTCTC[A/G]TGACCTCCATGGATA | 68497 |
rs213410037 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84968325 | TAAATACCGGTGGGC[A/G]GTGGTGGCACACGCC | 68497 |
rs213454543 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84967254 | GGTTTTTTTGTGAAG[A/G]CTAGAAGAAGGTGAC | 68497 |
rs213536941 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84923152 | CACTCTGTGACACTA[C/T]AGATATGTAAACACA | 68497 |
rs213580473 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84922423 | CTCCCATTCTCGGAT[A/G]TGTTGTCTCCAATGC | 68497 |
rs213582029 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84931517 | CATTCTGAACTGCTA[C/T]TGGTACATACTGATA | 68497 |
rs213625378 | in-del | -/AT | | | intron-variant | Arel1 | Mm_Celera | 12:84923082 | GCTAACTTTGGGCTG[-/AT]ACAAAATGTGAAATC | 68497 |
rs213664713 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84933831 | CCATATTCATTACAA[C/T]CTTCAAGCCTGTTAG | 68497 |
rs213709812 | in-del | -/ATTT | | | intron-variant | Arel1 | Mm_Celera | 12:84955556 | TCATATATTTTAAAG[-/ATTT]ATTTAATTTATGTTT | 68497 |
rs213843410 | in-del | -/TATATATATATATATG | | | intron-variant | Arel1 | Mm_Celera | 12:84963977 | ACACATGCATATATA[-/TATATATATATATATG]TATGTATATATTTAA | 68497 |
rs213905330 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84932503 | TAAATACCGTCCGGG[A/C]GTGGTGGCGCACACC | 68497 |
rs214058072 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84933648 | GGAAGGGCAAACGAA[C/T]GAGGGAATTTGAAGC | 68497 |
rs214101297 | in-del | -/AG | | | intron-variant | Arel1 | Mm_Celera | 12:84953350 | TTTTGTTTGAGATAT[-/AG]AGTCTCATGTAGCTC | 68497 |
rs214204437 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84952835 | AAAGACTTTAGAAGG[A/G]TGGTGGGAGACATTC | 68497 |
rs214254003 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84952289 | CTTAGGCGCAGATAC[A/T]GGACTACTTAATCAG | 68497 |
rs214257182 | snp | C/T | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84970081 | GCCCTGAGTTTGGTT[C/T]GCCCAGGATCTGGTT | 68497 |
rs214320568 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961947 | TCCTGGGTTCTATAG[C/T]TTTAAAGTCTTTGCC | 68497 |
rs214374586 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961551 | CATGAATCTGGAGTT[C/T]CCAGCAGTTGTGAGC | 68497 |
rs214375177 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84935681 | GCAAAATCAAAGGGC[A/G]TGAGACAGGTGCACA | 68497 |
rs214452567 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84955401 | TATTCTTAGAACAAC[A/T]AAGAATTTTATTTAA | 68497 |
rs214452638 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84946137 | ATACTCCTGCAAATA[C/T]AACCAAAATATATTA | 68497 |
rs214512098 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84954053 | AGTACACATTCTTAA[C/T]CACGGAGCCATCTCT | 68497 |
rs214591646 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84943280 | AGATAGGGAGGCAAA[C/T]AGGAACTCGACAACA | 68497 |
rs214737989 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84927537 | TGTTTCTTTAATGCA[A/G]CTCACTTATATGGTG | 68497 |
rs214740886 | snp | C/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971441 | TTTGCTTATAATGTC[C/T]TAGGTCTGTGTTGCA | 68497 |
rs214817357 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Arel1 | Mm_Celera | 12:84935068 | TGGCTGCCCACACGT[C/T]AACACCAGAGTAGAA | 68497 |
rs214871933 | in-del | -/TGTTC | | | intron-variant | Arel1 | Mm_Celera | 12:84933107 | ACCAATGTCCCTTTT[-/TGTTC]TGTTTTGTTTTTTCA | 68497 |
rs214888583 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84944641 | CTCACTTGGGTGTTA[C/T]TAGGACTTAGTGGGC | 68497 |
rs214985620 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84961923 | CACCGAGTCATTTAT[C/G]CAGCTCTGTCCTGGG | 68497 |
rs215161889 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84968786 | TTATAGGGTTGCAGA[A/C]CCCTTCAGCTCTTGG | 68497 |
rs215198546 | in-del | -/AAAT | | | intron-variant | Arel1 | Mm_Celera | 12:84961617 | CCCTGGAAAAGCAGA[-/AAAT]GTTCATAACTCGAAG | 68497 |
rs215246749 | in-del | -/C | | | intron-variant | Arel1 | Mm_Celera | 12:84939522 | CCTGGATCTGCCCCT[-/C]CCCCAATAAATAAGT | 68497 |
rs215284735 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84964514 | GACAGGGCCCCGTGT[C/T]CCCACCCCACAGCAG | 68497 |
rs215294512 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84944612 | TGTCAAATGGAGAGA[A/G]TACTCACAGGCACCT | 68497 |
rs215309292 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84962764 | TGTGTGTGTGTGGGG[C/G]GGGGGGTGCCTGTGG | 68497 |
rs215372094 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972238 | TGATCACTTCCTTGT[A/G]TTGAGTCTTTATTTT | 68497 |
rs215458462 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84926603 | TGTCCTGGAAGAGAA[C/T]TTCCAGGTCTCTCTC | 68497 |
rs215521309 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84935566 | CAAAGCTGCTCTCTA[A/C]TCTCTCTGTGCATAC | 68497 |
rs215527517 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972439 | GAAACTTGCTATGTA[A/G]ACCAGACCTCGAATT | 68497 |
rs215585546 | in-del | -/G | | | intron-variant | Arel1 | Mm_Celera | 12:84960132 | AGTGTGTCTGACACA[-/G]CCTTCTGATTTCACA | 68497 |
rs215660387 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84928936 | AATAAATAAATCTTT[A/T]AAAAAAAGTGTGGAC | 68497 |
rs215723243 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84938348 | ATGCCAGAAATATTT[A/G]TGTCCTTTAAAAAGC | 68497 |
rs215723276 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Arel1 | Mm_Celera | 12:84927909 | AAAGTTCTTGCTCCA[A/G]TCTGAGATGGAAAAG | 68497 |
rs215741101 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84924579 | CTGCAGCCCTGATAC[A/G]AACTTGCTACAGAAC | 68497 |
rs215781280 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84937086 | AATGCTACAGCCACT[A/C]TGGAAAAGAGTTTAG | 68497 |
rs215817627 | in-del | -/CC | | | intron-variant | Arel1 | Mm_Celera | 12:84939479 | GACTTTACATGCTGT[-/CC]CCCCCGACCTCCACA | 68497 |
rs215923723 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84951449 | TACACACACACACAC[C/T]ACCACCACCACCACC | 68497 |
rs215932259 | in-del | -/CA | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84918718 | AATGAGAGGTCTAGT[-/CA]CACACACACACTGAC | 68497 |
rs216101376 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84957808 | GCCAACTAACTAAGA[A/G]TGAGTGTGAGGGGCC | 68497 |
rs216166721 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84956868 | TAGGACCAAAAGGCT[C/T]CTTGGTTCTCTCCTG | 68497 |
rs216236456 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84965329 | AGTCTACGGGGAGGA[A/G]AGGCAGAGATTTATG | 68497 |
rs216238575 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84953012 | TATATATACATACAC[A/C]TTAATAAAAATATTA | 68497 |
rs216298222 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84964614 | GATCCTGACAAGCCG[C/T]CTCCCTCCACAAGTC | 68497 |
rs216300824 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84920013 | CAGACGGCTTGTGTG[A/G]GCCACTTTCTAGCTG | 68497 |
rs216437150 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84936989 | TATTTGGGAAATGCA[A/G]GTTAAACCTACACTC | 68497 |
rs216488085 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84945900 | ATGGAAGAAAGTGGT[A/G]GCATACTGTTGGCCA | 68497 |
rs216492431 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84935811 | GCCAGGCGGCGGTAG[C/T]GCATGCCTTTAATAC | 68497 |
rs216550434 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84945538 | ATGCCCTGTCTCCAC[A/G]CATTTTCAAAAAGCC | 68497 |
rs216604242 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84946088 | TATTTGGGGAGATAT[A/T]TTCTTCTGTGACGTA | 68497 |
rs216673639 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84954028 | GACTGACCTCGTCCT[C/T]GGGGAAAGCAGTACA | 68497 |
rs216720198 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947736 | GCTTAAGAAACATGG[C/T]GAACATACTACTCAA | 68497 |
rs216852880 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84940439 | CCATTAGTACAGAAG[A/G]GGGAGAGAACCACTT | 68497 |
rs216895603 | in-del | -/CAG | | | intron-variant | Arel1 | Mm_Celera | 12:84941988 | ACACAAACCACATTA[-/CAG]CGACTACAGAACAGA | 68497 |
rs216923757 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84927413 | CCCAATCCAAAGCTG[-/A]AAAAGTATAATGAAA | 68497 |
rs216964138 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947824 | TGTCTCACTCTAAGC[C/T]TGAAGACTAACAGTA | 68497 |
rs217005905 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947122 | TATCCTCATAAGCAT[C/T]CAGTCTAATTATAGA | 68497 |
rs217055236 | in-del | -/CAAACAAA | | | intron-variant | Arel1 | Mm_Celera | 12:84966703 | GGCTGTATAAACAAG[-/CAAACAAA]CAAACAAATGAAGTT | 68497 |
rs217081698 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84967231 | TATGTGTGTGTGTGT[A/G]TGTATGTGGTTTTTT | 68497 |
rs217250700 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84941146 | TGGCGTGGGCTTTCC[A/G]GCTCCATTTACTATA | 68497 |
rs217314199 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84940080 | CCTAGATCCTACCCT[A/T]CCTTACCAGAAAAGG | 68497 |
rs217334767 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948567 | CCCTTCCTTTGGGAG[C/T]CTACACACACACTGG | 68497 |
rs217514020 | in-del | -/TA | | | intron-variant | Arel1 | Mm_Celera | 12:84950747 | AAGTGTGTGTGCATG[-/TA]TATATATATTCAATA | 68497 |
rs217535989 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84927634 | ACACAGGTCAGAGAT[C/G]CAGGAAATGGACACT | 68497 |
rs217542779 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84932388 | TAGAGGTGTGGCCTT[G/T]TTGACAGGAAGAAGG | 68497 |
rs217615654 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84943079 | ACTTACCTACCTCCC[C/G]CTTCGTGTTGTGAAC | 68497 |
rs217627069 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84931689 | CTGCTCAGCACAAGG[C/T]CTGCCTTACCTTTGT | 68497 |
rs217629125 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84921491 | CCAATGATTCCTAAT[A/T]AGTGTGGGATTTCAA | 68497 |
rs217686021 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84942618 | GGAAGGAAGGACGGA[A/C]GGACGGACGGACACT | 68497 |
rs217718867 | in-del | -/C | | | intron-variant | Arel1 | Mm_Celera | 12:84943096 | TTCGTGTTGTGAACT[-/C]CTTACAGGCAGATTT | 68497 |
rs217901764 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84952942 | AACCACCTACAACTC[C/T]AAATCCAGGGGATCT | 68497 |
rs217935953 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84953716 | AAATCAGGACCTTTG[A/G]AAGAGCAGCCGGTGC | 68497 |
rs217971495 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84940921 | AACTATGCAGATGAG[-/A]AAGCAGCCGAAAGAC | 68497 |
rs218026002 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84922627 | CTGATGATACTGACA[A/C]TAGCGGTTTCCTTAC | 68497 |
rs218078218 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84921894 | CTAGGTGTTTCTGAC[A/G]AGTATGCCTAGTTAA | 68497 |
rs218103161 | snp | A/T | | | downstream-variant-500B | Arel1 | Mm_Celera | 12:84918120 | TGTAAGCATTGTCCC[A/T]CCCCCCACTCAAACA | 68497 |
rs218154977 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84927077 | ATAATAGCTTAATTA[C/T]TATAAGTGAGTAAAG | 68497 |
rs218283335 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84955468 | ACAATATATCTGAAG[A/G]AGCAAATAAATTATT | 68497 |
rs218329664 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84965062 | TTATGTGTGTGAGTG[G/T]TTTGCCTGCATGTAT | 68497 |
rs218354011 | in-del | -/G | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84970396 | CGGAGGGAGAACATT[-/G]GGGGGGGATGTCCTC | 68497 |
rs218377469 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84964546 | TTCTGTGATCAGGTA[A/G]CCGTGGACTACTCGA | 68497 |
rs218416895 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84942779 | CAGGCAGAGCTGAGT[A/G]TGTGGAAGGAGACCG | 68497 |
rs218434045 | snp | A/C | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947928 | GAACTTAGCCTAACA[A/C]AAAACCACTAACTTA | 68497 |
rs218466598 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84949605 | GATCACTGACCCACA[C/T]CCTCCACCACAGTAG | 68497 |
rs218485300 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84955901 | AACAAGATGGAATGT[-/A]AAAAAAAAAAAAAAG | 68497 |
rs218490676 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947442 | CAGGCTAACCTCAAA[C/T]TTACAGAGTTCCACC | 68497 |
rs218520644 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84949017 | GGACTACAAATTCCT[A/C]CAGCTTTTTTGTTAT | 68497 |
rs218542693 | in-del | -/GGGAGAT | | | intron-variant | Arel1 | Mm_Celera | 12:84953076 | AGAAGAGGAGGGCTG[-/GGGAGAT]GCTCAGCAGTTAAGA | 68497 |
rs218613161 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84928697 | ATCCCAGCAACCACA[A/T]GGTGGCTTACAATCA | 68497 |
rs218870723 | in-del | -/CA | | | intron-variant | Arel1 | Mm_Celera | 12:84960299 | TGCTGCTCTCGTATG[-/CA]CATACACATACATAA | 68497 |
rs218903249 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84951754 | GGCGTGGGAAGCATG[C/G]GGAGAGAACTGAGAC | 68497 |
rs218936950 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84930838 | CTGGAAGATTGAACC[A/G]GCTCACTAGGCTTGG | 68497 |
rs218941552 | in-del | -/AC | | | intron-variant | Arel1 | Mm_Celera | 12:84926097 | ATATAAGCAGGCAAA[-/AC]ACACACATACACACA | 68497 |
rs218974634 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84950956 | CTGCCACCCTCAAAG[C/T]CAGTGTACAATGTGA | 68497 |
rs218983246 | in-del | -/GC | | | intron-variant | Arel1 | Mm_Celera | 12:84935435 | CTCAAAAAACAAAAA[-/GC]CAAAAAAGTGCCAGG | 68497 |
rs218995771 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84921817 | CAGACAGATGAGTAC[A/C]CTAGGTACTGAAGCA | 68497 |
rs219094227 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84930114 | ATAGGAAGACATTAC[A/T]TACCGACTCCAACAA | 68497 |
rs219190385 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84958598 | GTGGGACAAGTCTTT[C/T]GTCTGCATTACATCA | 68497 |
rs219206169 | in-del | -/CCG | | | intron-variant | Arel1 | Mm_Celera | 12:84922389 | GAGCAGCCTGAGGAA[-/CCG]CTGTAGACTGCAGCT | 68497 |
rs219299415 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84965592 | ATTACAGTTTGACTG[C/T]AATGTGGAATTCTGG | 68497 |
rs219375811 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84921836 | GGTACTGAAGCAGAA[C/T]CTCTGAAGTTGGATT | 68497 |
rs219519151 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84949413 | ACATGGTGGCTCACA[A/G]CCATCTGTAATGGGA | 68497 |
rs219585212 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84949954 | GGAAAGGGTGCCCCT[C/T]TCTCACTTGAACCAC | 68497 |
rs219599144 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84959319 | ATTTAAGATTAGGAA[A/T]TTGAGGGACCCTGTC | 68497 |
rs219603664 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84960840 | GTAAGGAGTTTGTTC[A/T]TGAGTGCTGGGTAGT | 68497 |
rs219656825 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84960055 | GCAGCACTTTTCCAG[A/G]GGAGCCAGGTTTAAT | 68497 |
rs219740236 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84964703 | CCCAGTGGGGTAGAA[G/T]TTTGCAATTCTCTCT | 68497 |
rs219745682 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84953736 | GCAGCCGGTGCTCTT[-/A]AACTGCTGAGCCATC | 68497 |
rs219760589 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84943528 | TCTGCCACGCCCGAT[-/A]GGGGCCCTGTGCCAT | 68497 |
rs219773178 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84925655 | AGCAGCCTAGAGGGA[C/T]CCGGGCTGTAGGGGC | 68497 |
rs219792330 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84923488 | GAAAAGACTCATATA[C/T]ATTTTTAAAAATTTC | 68497 |
rs219846379 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Arel1 | Mm_Celera | 12:84931753 | GGGGATGATTTTCAG[A/G]TAGAATTCCTTCACA | 68497 |
rs219851153 | in-del | -/GTGTGTGTGTGTGTGTGTGT | | | intron-variant | Arel1 | Mm_Celera | 12:84930661 | ATATTTATTTATTTA[-/GTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 68497 |
rs219898471 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84931169 | CCACTGAGCCAACTT[C/G]CTGGCCCCTAGTTTG | 68497 |
rs219970434 | in-del | -/TTAC | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947533 | CAGTTTCTAAAACAT[-/TTAC]TTAATTACCAGTATA | 68497 |
rs220021422 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84928184 | CCAACTGGCTCCATG[C/T]AGCCAGGTGGGCAGA | 68497 |
rs220113448 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84937196 | TTATAAAAAAACCTA[C/T]ACATGAGTGTTAACA | 68497 |
rs220131705 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84945682 | AAAGAATGTTTACAG[C/T]CACAGGGCACTTTTG | 68497 |
rs220191047 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84953143 | CCCAGCAATCACCTG[A/G]TGGCTCACAACCATC | 68497 |
rs220260679 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84950692 | GAAACACTGAATCTA[C/T]TCAAACCAATTTACC | 68497 |
rs220300775 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84962471 | AAGCCACATTCCTCA[C/G]CAGTTCAATTAAAAC | 68497 |
rs220345605 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84930315 | CAGCTCTACAGGTAC[A/C]CGCCCCCATGGCTCA | 68497 |
rs220412731 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84940546 | TTCAGTTTTCAGTTC[C/T]GGTCTTAGAAACACA | 68497 |
rs220416321 | in-del | -/CAAG | | | intron-variant | Arel1 | Mm_Celera | 12:84966700 | CCAAGGCTGTATAAA[-/CAAG]CAAACAAATGAAGTT | 68497 |
rs220448787 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84965661 | TTTTGTGATATCCAA[A/G]TCTGTAGTTTAGTAA | 68497 |
rs220451223 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84933920 | TACAGCATAAGGGAC[C/T]AACAGTGATTTTTAT | 68497 |
rs220470506 | in-del | -/GTAT | | | intron-variant | Arel1 | Mm_Celera | 12:84927592 | CCTATAGATTCCAAG[-/GTAT]GTATTCTGGTCACTA | 68497 |
rs220572614 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84943442 | CTCCTTAAAGCCACC[C/T]CAGGAGACAAAGCAG | 68497 |
rs220629256 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84942854 | AGACCAGTCTGCTGA[C/G]CCTGTTGTCTATCAC | 68497 |
rs220654322 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84931859 | TACAAACACCAAAGC[C/T]TTGTCTATATTTTCA | 68497 |
rs220764010 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84929568 | ACAAAGCAAGGCTAC[A/G]TAGGGAGCCATGCCA | 68497 |
rs220839797 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84939145 | GGACAGATGCTCTTC[A/G]GGATGAAGTAAAATA | 68497 |
rs220927954 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84962412 | ATTCCAGAAGGTCAT[C/T]CTGTCTAGTTTAAGC | 68497 |
rs220956345 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84958744 | AATTTGATTTGAGAG[C/T]CTATGATATTAACCA | 68497 |
rs220981052 | snp | A/C | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971783 | AAACAAACAAACAAA[A/C]AAAGAATTCAGAACC | 68497 |
rs220981210 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84961854 | AAGTTACAGGTGTGA[A/C]GCGCCTGACAAGGTA | 68497 |
rs221033962 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84966528 | TGAGGGCCTCTGGCT[A/G]TAACTCAGTTGGTAG | 68497 |
rs221036881 | snp | A/C | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84970618 | CCCTCGTCCCCTCTT[A/C]TCTCGCTCGCCTTCA | 68497 |
rs221283057 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972035 | TTTAAAAAAAAAAAA[-/T]AAAAATAAATAAAGA | 68497 |
rs221285533 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84959911 | GTCTTGGGAACTATG[A/T]AGACCAGGCAGGCCT | 68497 |
rs221298860 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961029 | GGAACTGCTAGTTCA[C/T]AGGAGAAGCATATTT | 68497 |
rs221372118 | in-del | -/ACTG | | | intron-variant | Arel1 | Mm_Celera | 12:84924277 | TTTTCACTCTCTGTT[-/ACTG]ACTTTCAGGGCTCAC | 68497 |
rs221408944 | in-del | -/CCTGCCTGA | | | intron-variant | Arel1 | Mm_Celera | 12:84935370 | TCTGTGAGTTCAAGG[-/CCTGCCTGA]TCTACATGGTGAACT | 68497 |
rs221459437 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84963902 | GTACACTAGCTCCAG[A/G]GGATCTGATGCCCTT | 68497 |
rs221477270 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84920943 | ATACTGTGGGGAGGC[A/G]CATGCTCCCAGTTAC | 68497 |
rs221480089 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84930258 | AGGAGCAAGCAAGCA[C/G]CAAGGTTCATCATGA | 68497 |
rs221522174 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84929454 | TACATAAAATTTTTT[G/T]GGGTGTTTTTTTGGA | 68497 |
rs221582514 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84923609 | ATGGGCTTTCTTGCC[G/T]CACCACTAACAGAAG | 68497 |
rs221594527 | in-del | -/GTGTGTGTGTGTGT | | | intron-variant | Arel1 | GRCm38.p3 | 12:84930662 | ATATTTATTTATTTA[-/GTGTGTGTGTGTGT]GTGTGTGTGTGTGTT | 68497 |
rs221684110 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84927049 | TCCAATAGCCACAGG[C/T]GTTTTTCTTTGGATA | 68497 |
rs221687457 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84941386 | TATAGTTTAGAATGG[A/G]CTTTGAGACCCCCAT | 68497 |
rs221700044 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84961821 | CCTAAGCCGGGTTTC[A/C]TCAGGTCCCCTGCCG | 68497 |
rs221748637 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84926055 | TGCTTTCTACTCAGT[A/G]GGCACTGGATGTATC | 68497 |
rs221750995 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84935877 | GTAGAAGACCAGCCT[A/G]GTCTACAGAGTGGGT | 68497 |
rs221794990 | snp | C/G | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84970416 | GGGATGTCCTCCATC[C/G]CTATTACATTCCTCT | 68497 |
rs221836116 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84935254 | TTTCTGCACCAAACA[A/G]AATGAGAAAGAACTG | 68497 |
rs221995780 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84938786 | TGTGGCAAATGAAGT[A/G]GACAGTCTCTGAATG | 68497 |
rs222059603 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84937399 | CTTCAAACACTCTTC[A/T]TATGACTTAGTGGAG | 68497 |
rs222062428 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84924380 | AACGGTGCTGATGCA[A/G]CAGGAAGGTACTACG | 68497 |
rs222081319 | in-del | -/TGTGTGTGTGTGTG | | | intron-variant | Arel1 | Mm_Celera | 12:84936687 | ATCACGAAAGGAAAA[-/TGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 68497 |
rs222137525 | in-del | -/C | | | intron-variant | Arel1 | Mm_Celera | 12:84939732 | GGGACCTGAACAGTG[-/C]CTCGTGAGGTCAAAC | 68497 |
rs222142691 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84932604 | GAGTTCCAGGACAGA[C/T]AGGGCTATACAGAGA | 68497 |
rs222171339 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84945751 | TGGACAAGGGTAGCT[A/G]TACTCATGGCTAGTC | 68497 |
rs222182274 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84955740 | CCACAAGAGCAGCAC[A/G]TGATCTTAACCACCA | 68497 |
rs222234653 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84954510 | CTATACAGAGAAACC[C/T]TGTCTCAAAAAACAA | 68497 |
rs222307428 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972466 | AATTTTTAGGGCTCT[A/G]TCTGCCTCTCTCTCC | 68497 |
rs222313091 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84967792 | AGTCAAAACCATGCT[A/G]CCTTCCATCCCTATC | 68497 |
rs222375400 | snp | C/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972075 | CAGTTTCTCTGTATC[C/G]GTAAGGACTGGGTAA | 68497 |
rs222470757 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84965491 | CTCAACACTCACACA[A/C]ACACCCAAACCCCGA | 68497 |
rs222523881 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84964906 | CATGGGCCATGGCTT[A/G]TATAGCGGTCACAGG | 68497 |
rs222582575 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84944685 | TAGAACTGCAGTGAG[C/T]TTTCAGTCTTTGTGC | 68497 |
rs222687491 | snp | A/G | | | upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84970902 | GCCGGAAAGAGCGTG[A/G]GGATGACGTAAAGTG | 68497 |
rs222951000 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84942644 | ACACTGTAATGTGTA[C/G]AAAGGAGCTTCTAGA | 68497 |
rs222982183 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84933044 | TGCCTTAGACATGTT[C/T]TGCCTTGAACTACAT | 68497 |
rs223044353 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84943463 | GACAAAGCAGAGCAC[A/G]TGCCGTAAGCCTACC | 68497 |
rs223098902 | in-del | -/GC | | | intron-variant | Arel1 | Mm_Celera | 12:84927694 | TGGTGTGAACTGTAG[-/GC]GCTCACCCCCATGTC | 68497 |
rs223216320 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84929016 | AGGTTTTTTTCTCTC[-/T]TTTTTTCTTTTTTTT | 68497 |
rs223409692 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84962838 | TTGTTTTTTACAGAT[A/C]AGTTCTCTCAGCAGA | 68497 |
rs223486184 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84936110 | ATAACTACGATACCA[A/T]GCTTGTGAATTAAAG | 68497 |
rs223504982 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84967714 | CACTAAGAAGGACTA[A/C]AGTAATTCTTTCCCT | 68497 |
rs223552425 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84966769 | ATACACTAGACCTTT[A/T]CTTTAAAAACAACAA | 68497 |
rs223704485 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84919731 | CCACATGCCTGGACA[C/T]GGCCCTTCCCCACGA | 68497 |
rs223705313 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84931073 | GCAGTGAGTGCTGGG[A/G]CCATGTGCAACACAC | 68497 |
rs223755439 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84930364 | CAATGTTCTTGTGCA[A/G]GGAACGGATGAAAGT | 68497 |
rs223755944 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84941281 | ACTCATTATGCAGAC[C/T]AGGCTGGCCAGAACT | 68497 |
rs223810448 | snp | C/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971836 | TCCCATTATAAAGAA[C/T]ACTCAAGGGGCTGGT | 68497 |
rs223838960 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84940569 | GAAACACAGCGAGAG[A/T]CATGTTTATAAACAT | 68497 |
rs223884127 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84946545 | TGTAACAAAGCCTGC[A/G]ACCCCAGCCCTGTGG | 68497 |
rs223940131 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84945890 | AGAGGCAAAGATGGA[A/G]GAAAGTGGTAGCATA | 68497 |
rs224007393 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84953605 | TATTTACTATTATAC[A/G]TAAGTACACTGTAGC | 68497 |
rs224033997 | in-del | -/GGC | | | intron-variant | Arel1 | Mm_Celera | 12:84954858 | ACCCTTAGTGCTGCT[-/GGC]GGCATCAGAGACTAT | 68497 |
rs224040165 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84950246 | CAGCATGTTCACATC[-/T]TTTTTTTTTTAGATT | 68497 |
rs224061482 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84950433 | CATCTCTCCAGCCCC[C/T]GAACATTGATTTTTT | 68497 |
rs224071994 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84952840 | CTTTAGAAGGATGGT[G/T]GGAGACATTCCTCAG | 68497 |
rs224103590 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84949653 | CTATTAGCTCGGTGT[A/G]GAGATCAGGTTGCGC | 68497 |
rs224140826 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84960694 | GTTACAGACAGTTGT[A/G]AGCTGCCATGTGGGT | 68497 |
rs224180435 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84960000 | CTTGTTAAAAATAAG[A/G]CTCTTAAGGCATGGC | 68497 |
rs224185356 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84940997 | CTCATTGTGGCCCAC[A/T]CCTTTAATCCAAATA | 68497 |
rs224240309 | in-del | -/CTTTC | | | intron-variant | Arel1 | Mm_Celera | 12:84925606 | AGTACTCTGCAGAGT[-/CTTTC]CTTTCCTTCACTGCA | 68497 |
rs224255026 | snp | A/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948236 | TGAGGCTCTCCTGTA[A/T]AAGTGATTCTTGGGG | 68497 |
rs224372729 | in-del | -/AAGGAA | | | intron-variant | Arel1 | Mm_Celera | 12:84968051 | GATTTAAAATAAAAG[-/AAGGAA]AAAAAAAAAAAAAAA | 68497 |
rs224429663 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84951957 | ATTAAAACTCTGGGC[C/T]GGCATGGTAGTATGA | 68497 |
rs224591123 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84924803 | CCATAGCTAGAAGTG[C/T]TTATTCACAAAAACC | 68497 |
rs224755820 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972602 | TTTTTAGCATATATT[A/G]TACATAACAATAGAT | 68497 |
rs224786620 | snp | C/T | | | downstream-variant-500B | Arel1 | Mm_Celera | 12:84917761 | TTTAATCCCAGCATT[C/T]GGGAGGCAAAGGCAG | 68497 |
rs224800513 | in-del | -/CTCCAG | | | intron-variant | Arel1 | Mm_Celera | 12:84957902 | GCGGCTCACAACTTC[-/CTCCAG]CTCCAGCTCCAGAGG | 68497 |
rs224869636 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84918995 | GTCCTGATGCCAGGT[A/C]CCAAACCCCGAGGAT | 68497 |
rs224968498 | in-del | -/G | | | intron-variant | Arel1 | Mm_Celera | 12:84936352 | CCCTGGTACTGAGGA[-/G]GGGGCAGACACAACA | 68497 |
rs225029904 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84943501 | GTCTCGTGCCTTAAC[A/G]TCCCCATCCTCTCTG | 68497 |
rs225088342 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84943019 | TCCCATCAGTTAGGG[C/G]TTCCTTCTTTTGGGC | 68497 |
rs225123966 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972582 | CGTGGTTTGTTTTTG[-/TT]TTTTTTTTTAGCATA | 68497 |
rs225150107 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84949878 | TATATTGACTGGAGT[A/G]AGTTAGACCACAGGA | 68497 |
rs225178693 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84956555 | ACCCTCCTCTGTCCC[A/G]TGACATAATACTTCT | 68497 |
rs225181068 | in-del | -/ACAG | | | intron-variant | Arel1 | Mm_Celera | 12:84929276 | CGCCCTGGACAAAAC[-/ACAG]ACAAACAAAACCATC | 68497 |
rs225205818 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84945625 | AGAGAAGCTACAGCT[A/G]TAGTTGGGCTAAATG | 68497 |
rs225206470 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84949360 | GTTAAGAGCACTGAC[G/T]GCTCTTCCAGAGGTC | 68497 |
rs225216786 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84937461 | GGGCTGTGCATCCCT[G/T]GCTGGCTAAGGAAGA | 68497 |
rs225240769 | in-del | -/GAAACACAAGGA | | | splice-acceptor-variant | Arel1 | Mm_Celera | 12:84934401 | TTCTTCTCATTCTCT[-/GAAACACAAGGA]GTAAGGTTTGAAATA | 68497 |
rs225255660 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84964941 | TTTCCAGGAGCTGGT[G/T]CTCCCTCTCCACTGT | 68497 |
rs225255752 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84955239 | CTTTTCCCTCTCCTA[C/T]GGTTGGAGAACAGGC | 68497 |
rs225286027 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84946386 | CATTTACATTGTTTT[A/C]TTCTTGTTTTGTTTT | 68497 |
rs225412588 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84921517 | TTCAAAAAAACAAAA[A/C]AAAACAAAACAAAAA | 68497 |
rs225415097 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84930616 | TTTCCAAATACATAC[C/T]TGCCAGGAATACATA | 68497 |
rs225426473 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84938944 | AATGTCCTATTATTT[C/T]TGTGGATACCAAACT | 68497 |
rs225486595 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84929914 | TGTCAGTCTCCCCCA[C/T]AGTTGCATGCCTCTA | 68497 |
rs225505631 | snp | C/G | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947337 | AAGTCTACCACTAAG[C/G]TACACTCCTAACCCT | 68497 |
rs225553167 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84925902 | CCATTTACACCTTCA[A/G]CCTTAAAAATAATCA | 68497 |
rs225613491 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84935172 | AGATTCACAGAATGA[A/G]CTGTGAAGACTTGGT | 68497 |
rs225740078 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84962497 | AAAACTTAGCCTAAT[A/G]AAGCTTAAGATGACC | 68497 |
rs225760683 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961174 | CCAGATTTTACTCAT[G/T]CTCATAGCTGATCCT | 68497 |
rs225817085 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84928246 | GTAGGGCATAGCATT[C/T]CTGAGATGACCCCAG | 68497 |
rs225866078 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84926814 | AACAGAAAGCTGACT[C/T]ATACCCAATGCTAAG | 68497 |
rs225897226 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84924513 | CCTCTATCACCCAAG[C/T]ACACAGATGGAAAGA | 68497 |
rs225943442 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84959167 | TAAGCCAGTAAAACT[C/T]ACAATCTTAGGAGAA | 68497 |
rs226005591 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84957841 | TGGTTAAGAGAGCTC[A/G]TTGCTATGTAGAGAG | 68497 |
rs226020205 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84925132 | GTTGGGATCAAAGTG[C/T]GTCATCACACTCAGC | 68497 |
rs226096409 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Arel1 | Mm_Celera | 12:84934278 | TTGAGAAGAGCTCAT[A/G]TGCATGGGAGGAAGA | 68497 |
rs226104449 | in-del | -/AGAAGGCGGC | | | intron-variant | Arel1 | Mm_Celera | 12:84934947 | CTGGACGGGGAAGAG[-/AGAAGGCGGC]ACTCACCTCGTGAAT | 68497 |
rs226124333 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84953282 | TAATGGTTGACATCT[C/T]TTGGAATACATGTAA | 68497 |
rs226170264 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84922039 | CTCTCAGGTCTAGCC[C/T]CCTTTCGTGGGCTGA | 68497 |
rs226174120 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84952306 | GACTACTTAATCAGA[C/T]TTTACAGTCCAGACG | 68497 |
rs226199069 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84963060 | GCCGGCCTTTATCTC[C/T]GGATTCTCCTGCATC | 68497 |
rs226243120 | in-del | -/TTTTCTTGAAGA | | | intron-variant | Arel1 | Mm_Celera | 12:84924447 | AAACCACTCATGGCC[-/TTTTCTTGAAGA]TGCTCTTTCATATGG | 68497 |
rs226387861 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84952019 | ACGCAGGATGAGCAC[A/G]AGTCCCAAGACCAAA | 68497 |
rs226394503 | in-del | -/AGA | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84920312 | GTGGTGAACGTGGAC[-/AGA]AGGTGAGGTAAGAAC | 68497 |
rs226432879 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84951169 | AAAAGAAAAGAAAAA[A/G]AAAAGGCCAAAAAGT | 68497 |
rs226434389 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961876 | GACAAGGTAGTGGGA[C/T]GGGACCTGCAAGAAC | 68497 |
rs226445642 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84964269 | ATTTTTTTAAGCTCC[-/T]TTTTTTATATATTCA | 68497 |
rs226448422 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84956145 | CCCAGCACTCTGGAG[C/G]CAGAGGCGGGCGGAT | 68497 |
rs226494681 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84968106 | GGCTTTTCTTTCAGT[C/T]CCTGAATTTAAAAGC | 68497 |
rs226499324 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84954437 | GGAGGCAGAGGCAGG[C/T]GGATCTCTGAGTTCA | 68497 |
rs226576149 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84963858 | CCGAGTCCAGTTCCC[C/G]GCACCCATGCCAGGT | 68497 |
rs226619810 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84926426 | CACCTGTCAAAGAAA[C/T]GAAAACGTCTTTGAC | 68497 |
rs226676739 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84925411 | TATCAAATTTAAGGA[C/G]AGCCTGTGCTACAGA | 68497 |
rs226705590 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84931489 | GTGATGAAGACAGAA[G/T]ACACTGGGAACACAT | 68497 |
rs226753229 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948011 | AGAGTATGACCTCTG[C/T]AGATGACCAGGTTGC | 68497 |
rs226788176 | in-del | -/AC | | | intron-variant | Arel1 | Mm_Celera | 12:84946350 | TAGATTTATATATAT[-/AC]AACTTTTAAAAATTT | 68497 |
rs226823044 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84957325 | TCTAGATGCTTACAC[A/T]TGGTCCTATCATAGA | 68497 |
rs226831311 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84941127 | CATGAAACAGAAACT[A/G]GGCTGGCGTGGGCTT | 68497 |
rs226872480 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84923352 | AAATACTCATTAGTC[A/T]ATTAATATCAATAAT | 68497 |
rs227118934 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961068 | CAAGAAACGACCCAG[C/T]TGCTTCCCCAGGCAG | 68497 |
rs227156588 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84929317 | GATTTAAAAGTTAGA[A/C]TTGTTTTATTTTTCT | 68497 |
rs227172485 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84960341 | ACTCGTGTGCACATA[C/G]CCGAACATGCATAAA | 68497 |
rs227174136 | snp | C/T | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969545 | CGAACACCTCTGAAC[C/T]CAGTAACACTAGGTC | 68497 |
rs227187184 | in-del | -/CAGGTTCTTCCC | | | intron-variant | Arel1 | Mm_Celera | 12:84950665 | TTCCTACCAGCTGCA[-/CAGGTTCTTCCC]CAGGCCTCTCTGAAA | 68497 |
rs227233873 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84936933 | AAAGATGATAACATA[A/G]CTGTCAGATGAGCAC | 68497 |
rs227254837 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84968052 | GATTTAAAATAAAAG[-/A]AAAAAAAAAAAAAAC | 68497 |
rs227270432 | in-del | -/ATAA | | | intron-variant | Arel1 | Mm_Celera | 12:84923372 | TATCAATAATACTTG[-/ATAA]ATAAATATTAATGAC | 68497 |
rs227343357 | in-del | -/C | | | intron-variant | Arel1 | Mm_Celera | 12:84930318 | CTCTACAGGTACACG[-/C]CCCCATGGCTCACCG | 68497 |
rs227383463 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84924614 | GTCTAGTAGCTGTTT[C/G]TTCCTTAACACACAC | 68497 |
rs227385596 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84934446 | GCAACCTGACCTTCT[A/G]ATGGTCACTTCATGT | 68497 |
rs227409867 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84922734 | CTGTCCTGGAACTCC[A/C]GAGTGCAGGAAGGAT | 68497 |
rs227459696 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84933477 | GGCCAGCCTGGCCTA[C/T]AGAGCAAGTTCCAGG | 68497 |
rs227522983 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84962566 | AGTCTCTTTGCATCA[G/T]TCTCTTTAAAACAAA | 68497 |
rs227553755 | in-del | -/TTC | | | intron-variant | Arel1 | Mm_Celera | 12:84968272 | GTCTCCAGATGGTTT[-/TTC]TTTTTTTAATAATTG | 68497 |
rs227593395 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84964505 | CAGGAGGAGGACAGG[G/T]CCCCGTGTCCCCACC | 68497 |
rs227745873 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84928366 | GAAGAGAGGTGGAAC[C/T]GGAGATTCCAGGCAC | 68497 |
rs227798998 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84927498 | CTTGTAGCATTCTCC[C/T]GTCCTTCTCTCTAGT | 68497 |
rs227851508 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84936628 | AGTGGAGAAAAGTCT[C/T]TAGGATCCAGAATTA | 68497 |
rs227885327 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84964522 | CCCGTGTCCCCACCC[C/G]ACAGCAGCTTCTGTG | 68497 |
rs227931887 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84963482 | AGAAATACCTGCCCA[A/T]GCAGTGCTTCCCCAA | 68497 |
rs227952319 | snp | G/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972096 | GACTGGGTAAACAGT[G/T]AATTTAATGAAGACT | 68497 |
rs227954461 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961931 | CATTTATGCAGCTCT[G/T]TCCTGGGTTCTATAG | 68497 |
rs227956130 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84953242 | TAATAATTTTTTTTT[-/A]AAAATCAGAGGAAAA | 68497 |
rs228013319 | snp | C/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971357 | GCTAAGTAGAAACAT[C/T]TGATGTACTGGTTTC | 68497 |
rs228090360 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84925290 | ACATAACTCCACAAT[A/G]TAACAAAAACATATT | 68497 |
rs228162980 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84927610 | ATTCTGGTCACTAAG[A/C]TAACAGAAACACAGG | 68497 |
rs228282992 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84922941 | GAGGCAGAGACAGGC[A/G]GATTTCTGAGTTCGA | 68497 |
rs228286528 | in-del | -/ATATATATATAT | | | intron-variant | Arel1 | Mm_Celera | 12:84963970 | TACTGACACACATGC[-/ATATATATATAT]ATATATATATGTATG | 68497 |
rs228311009 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84965021 | TCAACCTGATGCGCT[A/G]TGTTGCTGGCCCTCC | 68497 |
rs228338586 | in-del | -/C | | | intron-variant | Arel1 | Mm_Celera | 12:84937291 | AAACAAATACCCATA[-/C]CACTGAATGGTACCC | 68497 |
rs228369436 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84931427 | GAGTGAGCTCCAGCA[C/T]ACCGGAGACTATGAA | 68497 |
rs228417457 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84970962 | GGAGTGCGGCGTGAA[A/C]ATGGTGAGCGGAGTG | 68497 |
rs228451026 | snp | C/G | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969847 | AAAACCAAACACTGC[C/G]CAGTTTCGCTTTCTC | 68497 |
rs228526975 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972581 | ACGTGGTTTGTTTTT[-/G]GTTTTTTTTTAGCAT | 68497 |
rs228642736 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84939783 | GTTTATGATTACACT[A/G]ATAGAACTGGCCAGA | 68497 |
rs228672974 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84936304 | GTAAGTGGAGGAGAG[C/T]AGTGCCTGTGATCTG | 68497 |
rs228676556 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84928564 | GAAGCCAGAGGCCTC[A/G]AATCACTGCAATGAG | 68497 |
rs228718080 | in-del | -/TGTG | | | intron-variant | Arel1 | Mm_Celera | 12:84961489 | ACTTGTATGAATATT[-/TGTG]TGTGTGTGTGTGATA | 68497 |
rs228730802 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84935490 | GAGGCACCCTGCCAG[C/T]ATGCTGACCTACGTG | 68497 |
rs228747591 | snp | A/C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84937591 | AATGGAAAATAGAAA[A/C/T]GCATGAAATTCAAGA | 68497 |
rs228790395 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84934562 | CCAAGTCACAGCTTT[C/T]AACTCACCACTAAGG | 68497 |
rs228793111 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84945307 | TGCTCCAAGTCTCCC[C/T]AAGGTCACATCCTGA | 68497 |
rs228847041 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84944518 | ACAGATGCCTCCATC[C/T]TTCAGTCAGATTCAT | 68497 |
rs228920103 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84939279 | CCCTCCAGAGCTATC[A/G]GACTGACTACTCAGC | 68497 |
rs228972800 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84938343 | GTACAATGCCAGAAA[C/T]ATTTGTGTCCTTTAA | 68497 |
rs228975002 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84930813 | GGTTCTCTTCTTTCA[C/T]CACATGGGTCTGGAA | 68497 |
rs228993440 | in-del | -/G | | | intron-variant | Arel1 | Mm_Celera | 12:84922892 | GGTGTTTAGCCAGGC[-/G]GTGGTGGCACACACC | 68497 |
rs229034289 | snp | A/G | | | intron-variant, utr-variant-5-prime | Arel1 | Mm_Celera | 12:84946868 | AACCAGGAAGGCATG[A/G]TGCTCAAGAAGGAGC | 68497 |
rs229092133 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84945948 | ACACTTTTGAACTCA[C/T]GGGAGCTATGGCTAC | 68497 |
rs229111474 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84960216 | TAAAAAACTAAAGTT[C/T]TTAACATAAAAAACA | 68497 |
rs229197264 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84968054 | TTTAAAATAAAAGAA[A/G]AAAAAAAAAAAACAG | 68497 |
rs229298687 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84932298 | GTGTGAGCTACCATG[C/T]GTGGCTCTTTCTTCC | 68497 |
rs229336431 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84930724 | TGTGTGGGTGTGGGG[-/T]GTGTGGGTGGGGGTG | 68497 |
rs229374864 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84921513 | GGATTTCAAAAAAAC[-/A]AAACAAAACAAAACA | 68497 |
rs229385871 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84965701 | TACCAATTCTTAGAC[A/G]TGACAGATGTACCGT | 68497 |
rs229420469 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84965048 | TCCACTCTCTTTTTT[-/A]ATGTGTGTGAGTGGT | 68497 |
rs229437563 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84965285 | ATGTAACTGAAAGGA[A/G]AACAATCTTTTTTTC | 68497 |
rs229502755 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84940789 | CGGGGGCGACTCAGG[C/G]TCATACACCAAACTT | 68497 |
rs229612127 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84959273 | CACAGACTTGTAGTT[C/T]CAACTATCGTGGAGG | 68497 |
rs229671571 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84967014 | TTGTTTTAACAATAA[C/T]TAGCATGTTGTCTGG | 68497 |
rs229781013 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84944673 | AACACGTCAGCCTAG[A/G]ACTGCAGTGAGCTTT | 68497 |
rs229817954 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84952300 | ATACAGGACTACTTA[A/T]TCAGACTTTACAGTC | 68497 |
rs229867630 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84951650 | CCTCAAACGCCCCAG[G/T]CTTTCAGCAGACGTA | 68497 |
rs229951911 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84939426 | AAGCCTGCTGGCCTG[A/C]GTGTGATCCCCAGAA | 68497 |
rs230001356 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84962026 | AAAAGTTTCATAAGG[-/A]AAAAAAACCTCTTGT | 68497 |
rs230031278 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947199 | GTCAACTGTCTGTTC[C/T]TTTCTTACCTCAGAT | 68497 |
rs230092709 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84955434 | ATTTCCAAAGGCTAA[A/G]CAAGAGGATTTTTGT | 68497 |
rs230092771 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84946147 | AAATATAACCAAAAT[A/G]TATTATATAGATATA | 68497 |
rs230203599 | in-del | -/AAAAAA | | | intron-variant | Arel1 | Mm_Celera | 12:84966788 | AAAAACAACAACAAC[-/AAAAAA]AACAAAAAAAACCAG | 68497 |
rs230219459 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84941489 | AACCAGCCTCAACAC[-/T]TTTTTTTTATTTGAA | 68497 |
rs230259075 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84941990 | ACAAACCACATTACA[A/G]CGACTACAGAACAGA | 68497 |
rs230288356 | in-del | -/GG | | | intron-variant | Arel1 | Mm_Celera | 12:84968053 | TTTAAAATAAAAGAA[-/GG]AAAAAAAAAAAAACA | 68497 |
rs230362933 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84946182 | ATTAATAATGTCAAT[-/A]AAAACTTTGTAAAAA | 68497 |
rs230380286 | in-del | -/TGTGTGTGTGTGTGTGTG | | | intron-variant | Arel1 | Mm_Celera | 12:84936686 | ATCACGAAAGGAAAA[-/TGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 68497 |
rs230397425 | in-del | -/CAAACAAAGA | | | intron-variant | Arel1 | Mm_Celera | 12:84946674 | GAGGTGAAAAGCCAT[-/CAAACAAAGA]CACTTATCAACCTTG | 68497 |
rs230403641 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84921682 | GTTGGATCCCTAGAA[C/T]GCACAGTGGAGGGGT | 68497 |
rs230558088 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84965932 | GAAGGTCTCCATTGC[A/T]TTTTCTTCCAAATAG | 68497 |
rs230826105 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84932105 | TGACTCCCCAAGCCC[A/C]CACACAGGAGCAAAC | 68497 |
rs230867840 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84942606 | GGAAGGAAGGAAGGA[A/C]GGAAGGACGGACGGA | 68497 |
rs230874496 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84942895 | CACAACCCCTCCCAC[C/T]GTCCTGCCATGCTGC | 68497 |
rs230882142 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84968388 | CGGATTTCTGAGTTC[A/G]AGGCCAGCCTGGTCT | 68497 |
rs230956490 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84941244 | TTAAGATAAGGTCAC[A/C]CAGCATAGCCCTGAC | 68497 |
rs231035439 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948727 | ACCAAAGTCCAGATT[A/G]TTCTCAATTCTGAGC | 68497 |
rs231082704 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84934526 | GAACAGATATACAAA[A/G]AGGAAATGGCTAGAA | 68497 |
rs231113247 | in-del | -/TGCAGTTCTCC | | | intron-variant | Arel1 | Mm_Celera | 12:84955919 | AAAAAAAAAAAAGAA[-/TGCAGTTCTCC]AATGTATTCTCCAAT | 68497 |
rs231130880 | snp | C/G | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947987 | TTGTTGGAAACAATG[C/G]ACAGTTCTAGAGTAT | 68497 |
rs231138057 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84944453 | CATCAGAGTACTGAC[A/C]GCTCTAAAGGCAGAG | 68497 |
rs231154209 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84931581 | AGAGTTATATGTCCA[C/T]GGCCTTTAATGAGGA | 68497 |
rs231314716 | in-del | -/GGAC | | | intron-variant | Arel1 | Mm_Celera | 12:84933973 | CAGCAGCAGCGGTGG[-/GGAC]CTCCAGTTCCATGCA | 68497 |
rs231318848 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84935342 | AGCACTCAGAAGGCA[C/G]GGGCAGGTGGATCTC | 68497 |
rs231407995 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84923786 | GACCTCCATATACCC[G/T]ACTGGCACCCGTGTG | 68497 |
rs231418366 | in-del | -/AAC | | | intron-variant | Arel1 | Mm_Celera | 12:84932646 | AAAAAACAAAAACAA[-/AAC]AAAACAAAACAAAAC | 68497 |
rs231424978 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84919091 | CTAGCAGCTCAGGAG[A/G]GCTTGTTTCTCGTGA | 68497 |
rs231424989 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84928937 | ATAAATAAATCTTTA[A/T]AAAAAAGTGTGGACC | 68497 |
rs231459689 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84930996 | TGCCTTGCTGGATAA[A/T]CACTCCAGGATGCCT | 68497 |
rs231513220 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84930286 | TGACTTACTCTCAGG[C/T]GTGCGATGGAGCACA | 68497 |
rs231524302 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84927997 | TGGCTGCTCCCTCAG[C/T]TTCTAAAGAGAACCC | 68497 |
rs231534111 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84943892 | AAAGGAGGAGTCATT[C/T]GTGACATTACCAGAT | 68497 |
rs231637537 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84949118 | ACTCGATGATGCAGG[A/G]TCACAGGCAAGCTGC | 68497 |
rs231799054 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84950123 | GTGGATCTTGTCCCA[C/T]TCTTCGCCTCACTGG | 68497 |
rs231818338 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84926531 | AAGGTGTATATATTT[-/A]AAAAGTTTTGGTCCC | 68497 |
rs231821708 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84943634 | GATTTAGTGCTAGCT[A/T]CATATGAAATGATAC | 68497 |
rs231830326 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84944150 | ACAATTTGAAAAGGG[-/A]AAAGGAGAACAGGCA | 68497 |
rs231862219 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84960436 | CCAGTAAGCTCTTTG[C/G]AATTCAATCCAGGGA | 68497 |
rs231862256 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84949550 | AATCTCACTGCAGCC[C/T]GTGTTCCCCCCGTTC | 68497 |
rs231878024 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84950991 | ACTGTTCTCCAGCCG[A/T]TAGACATTGTGGAAA | 68497 |
rs231880535 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84923020 | GAGAAACCCTGTCTC[A/G]AAAAAACAAAACAAA | 68497 |
rs231911505 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84959521 | TGGATACCAGGTGTG[A/G]GCATGATGCACTTAC | 68497 |
rs231941672 | in-del | -/AA | | | intron-variant | Arel1 | Mm_Celera | 12:84923038 | AAAACAAAACAAAAC[-/AA]AAAAAAAATGGTATT | 68497 |
rs232019876 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84918754 | TGTGTAGTCTGCAGA[-/G]GGGTGCTGGAGCCTG | 68497 |
rs232050926 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84945346 | TCCTCTCCATCTCCC[G/T]CCCTCTCCTTCCTCC | 68497 |
rs232062540 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84923215 | CACTAGCATAGAGCC[C/T]GGAGGGACTTCTGTC | 68497 |
rs232121754 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84922435 | GATGTGTTGTCTCCA[A/G]TGCTCACACTACAAC | 68497 |
rs232140920 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84956907 | TGTCCTCTGCCAAAG[G/T]CCTTAAAGCTCTTGT | 68497 |
rs232177621 | in-del | -/CCTGTTAA | | | intron-variant | Arel1 | Mm_Celera | 12:84945990 | TTGCATATGATGGAG[-/CCTGTTAA]CATCCTAGCATGGAG | 68497 |
rs232183371 | in-del | -/CGCA | | | intron-variant | Arel1 | Mm_Celera | 12:84961793 | GTGTGTGTGTGTGTG[-/CGCA]TGCGCAGCACCTAAG | 68497 |
rs232231966 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84955767 | ACCAAGCCATCTTTC[C/T]AGTCTTTAAAATGCT | 68497 |
rs232235760 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84965369 | TTAGCCTCAAGCTCG[A/T]TATGTAGCTGAGGAT | 68497 |
rs232324099 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84964653 | GTTATTTTATTAACC[A/G]CCGTGAAATGGCAGG | 68497 |
rs232440406 | in-del | -/TT | | | intron-variant | Arel1 | Mm_Celera | 12:84963017 | AGCTGGTCTGCTTGA[-/TT]TTTTTTTAGAAGTCT | 68497 |
rs232456790 | in-del | -/AAA | | | intron-variant | Arel1 | Mm_Celera | 12:84958900 | TAGATTTTAAGCAAC[-/AAA]AAAAAAAAAATATTT | 68497 |
rs232484572 | in-del | -/AAAAC | | | intron-variant | Arel1 | Mm_Celera | 12:84921508 | GTGTGGGATTTCAAA[-/AAAAC]AAAACAAAACAAAAC | 68497 |
rs232494925 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84950007 | CACGCACGCATGTGT[A/G]TTGCACAGTAGTTTC | 68497 |
rs232578094 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84967235 | TGTGTGTGTGTATGT[A/G]TGTGGTTTTTTTGTG | 68497 |
rs232587019 | in-del | -/AA | | | utr-variant-5-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84951144 | TAACTTGCACATTTG[-/AA]AAAAAAAAAAAAAGA | 68497 |
rs232632871 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84966248 | ATGAACACAGACACA[A/T]GTGTACACACACCCT | 68497 |
rs232678928 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84953414 | AGGCCTTGACCTGAT[A/G]TGTACCACTATGCAT | 68497 |
rs232690948 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84965512 | CAAACCCCGACAGAT[C/T]GGAAGCTATGGAGAG | 68497 |
rs232737967 | in-del | -/GCTG | | | intron-variant | Arel1 | Mm_Celera | 12:84962923 | CTCTCTCTCCTCAGA[-/GCTG]GCATCACAGACCTGT | 68497 |
rs232747541 | in-del | -/GTAT | | | intron-variant | Arel1 | Mm_Celera | 12:84955592 | AGGGTTTGCCTGCAG[-/GTAT]GTATGTATGTATGTA | 68497 |
rs232778907 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84930844 | GATTGAACCGGCTCA[C/T]TAGGCTTGGCTGGCA | 68497 |
rs232794614 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84952151 | GTGGGTGCACATATA[C/G]AAAGAGCTACCATAA | 68497 |
rs232831506 | in-del | -/ACAAAAC | | | intron-variant | Arel1 | Mm_Celera | 12:84956273 | ACAAACAAAAAAAAA[-/ACAAAAC]AAAAAACAAAACCAA | 68497 |
rs232846897 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961911 | AGTGCTCTTAACCAC[C/T]GAGTCATTTATGCAG | 68497 |
rs233079863 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84924691 | ACAATTACCCTGGAG[A/G]GTCTGTATGGAAACC | 68497 |
rs233099558 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84933402 | TCTACAGGAAGGCTC[A/G]ATTTGTTAATACATA | 68497 |
rs233165778 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84924366 | TCTCTCAGGCAGTGA[A/G]CGGTGCTGATGCAAC | 68497 |
rs233259169 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84919627 | GCTAAAGACAGCTCT[A/T]AACAAACTATGTAAG | 68497 |
rs233294740 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84926571 | GCACCGTCTGTAGCG[C/T]TCAGGCTACTGAGGT | 68497 |
rs233318490 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84933944 | TTTTTATCCTCACAC[A/G]AAACAAACCACTTCA | 68497 |
rs233462683 | in-del | -/CCTCAGGTTACGG | | | intron-variant | Arel1 | Mm_Celera | 12:84956956 | ACACACTTCTTCTGA[-/CCTCAGGTTACGG]CCCACTACCACCTAT | 68497 |
rs233503580 | in-del | -/A | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942068 | TAAGAACGAAGGAGG[-/A]GAGGGAGGGAGGAAA | 68497 |
rs233539531 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84928700 | CCAGCAACCACATGG[C/T]GGCTTACAATCACCT | 68497 |
rs233573822 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84945764 | CTATACTCATGGCTA[C/G]TCAAATGATAAGAAT | 68497 |
rs233597805 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84954038 | GTCCTCGGGGAAAGC[A/C]GTACACATTCTTAAT | 68497 |
rs233600389 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947490 | TACTGGGATTAAAAG[C/T]GTGTGGCCACCACAT | 68497 |
rs233651385 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84963596 | GGCAAGTGGACTGCT[G/T]TTCCGTGTACAGGGC | 68497 |
rs233651430 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84953070 | AAAAATCAGAAGAGG[A/G]GGGCTGGCTCAGCAG | 68497 |
rs233709844 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84962779 | CGGGGGGTGCCTGTG[A/G]AAGCCAGAGGTCACA | 68497 |
rs233774970 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84953822 | CTCTGCCTCCTTCAG[C/T]AAATCCTACTGGCAT | 68497 |
rs233792172 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84961267 | GCTTCTGTCTTCCAC[A/G]TGCTGGAATTAAAGG | 68497 |
rs233847826 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84963514 | TACAGAATGGCACGA[C/T]ATAATGCTGCTTTAG | 68497 |
rs233859575 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84926705 | AAACCCAAAAGCAAG[A/G]AGGCTGGCCAGCCAT | 68497 |
rs233915972 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84925635 | ACTGCAGAAGGTCCT[A/G]CCGGAGCAGCCTAGA | 68497 |
rs233918372 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84958990 | GGTGGCAGTGCCAGC[C/T]GTCCCTGCAAGTCAG | 68497 |
rs233969541 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84944027 | CCAGAGTCTGAGGGG[A/G]AATTTTCACTGTTAC | 68497 |
rs234025735 | in-del | -/TT | | | intron-variant | Arel1 | Mm_Celera | 12:84932955 | AAAGATAATGCAAGA[-/TT]TTTTTTTTTAAATCT | 68497 |
rs234123774 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84921933 | AAGGTGGCTTTGTCA[C/T]TACAGAATGAAATGA | 68497 |
rs234153595 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84918309 | GGTCTCCTTCAAGGA[C/T]ACCAAAAAGCCAAAA | 68497 |
rs234155016 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84932472 | GAGAAGTAGAGTGGG[A/G]CTTCACAAAAAAATC | 68497 |
rs234297565 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84942622 | GGAAGGACGGACGGA[A/C]GGACGGACACTGTAA | 68497 |
rs234485911 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84952621 | CCAGTTTAAAGGATC[A/T]GCAAACACGGGAATA | 68497 |
rs234518656 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971642 | CCGGGCGGTGGTGGC[A/G]CACGCCTTTAATCCC | 68497 |
rs234544704 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84953233 | TACATAAAATAATAA[-/T]TTTTTTTTAAAAATC | 68497 |
rs234719636 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84937203 | AAAACCTATACATGA[A/G]TGTTAACAGTAGCTT | 68497 |
rs234728843 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84960733 | CTGAAACCAGGTCGG[C/T]CCTCTGAGAGCAGCA | 68497 |
rs234728985 | snp | A/G | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84970007 | TGATCGTCTAAAAAA[A/G]GCCACTGCGACTGGG | 68497 |
rs234751518 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84933839 | ATTACAATCTTCAAG[C/T]CTGTTAGTGACAACC | 68497 |
rs234791682 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84968855 | CATCCTATAGATGAC[A/G]GTGAGCATCCACTTC | 68497 |
rs234803106 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84955149 | AAAATTATTTTCTTC[C/T]CATTCTACTATACCT | 68497 |
rs234916653 | in-del | -/AA | | | intron-variant | Arel1 | Mm_Celera | 12:84956264 | AACAAACAAACAAAC[-/AA]AAAAAAAACAAAACA | 68497 |
rs234927358 | in-del | -/TTTATT | | | intron-variant | Arel1 | Mm_Celera | 12:84964389 | TAACTCAATAACAAA[-/TTTATT]TTTATTTTTAAAGGA | 68497 |
rs234969144 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84962888 | GATAAACTGGCTGGC[C/T]GTCACCACTCCCTAC | 68497 |
rs234984679 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84960892 | GAGGCTGCTTATCCA[-/T]TCACCAGATGGACAC | 68497 |
rs235020492 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84932956 | AAAGATAATGCAAGA[-/T]TTTTTTTTAAATCTG | 68497 |
rs235027958 | in-del | -/ATT | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972621 | ATAACAATAGATATC[-/ATT]ATGTTATTTTTCAAG | 68497 |
rs235028246 | snp | C/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972449 | ATGTAAACCAGACCT[C/T]GAATTTTTAGGGCTC | 68497 |
rs235035433 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948446 | TTGGCTCTGGTCCAC[A/C/G]TGTCCTCTGCAATCT | 68497 |
rs235047492 | in-del | -/AG | | | intron-variant | Arel1 | Mm_Celera | 12:84958456 | GCTATACTCTCCCCA[-/AG]AGATTAGCTGGTTTT | 68497 |
rs235089712 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84957666 | GCTCACAGATGAACG[C/T]GATTCACTGTGGAAA | 68497 |
rs235191255 | in-del | -/AAAAACAAAAAC | | | intron-variant | Arel1 | Mm_Celera | 12:84935423 | AATGACCATATCTCA[-/AAAAACAAAAAC]AAAAACAAAAAGCCA | 68497 |
rs235192256 | in-del | -/GAAA | | | intron-variant | Arel1 | Mm_Celera | 12:84931782 | AGAGAATTGCTGGGG[-/GAAA]GACCACACAGAGAAT | 68497 |
rs235225195 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84929407 | TTTTTTTTTTTTTTT[A/T]AACAAATTTCATTTT | 68497 |
rs235228172 | in-del | -/TG | | | intron-variant | Arel1 | Mm_Celera | 12:84961490 | ACTTGTATGAATATT[-/TG]TGTGTGTGTGATACC | 68497 |
rs235304001 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84924858 | TATCCATAATTATAG[-/A]AAAAAAAAGTTCTAC | 68497 |
rs235328705 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84930094 | TTCTTAGCTGCAGAA[A/C]CTGCATAGGAAGACA | 68497 |
rs235448778 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84968586 | CTATTCCCTCCCCCC[A/G]CCCTGCTCCCCTACC | 68497 |
rs235495391 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84923272 | TCAGCACACAGCTCA[G/T]AGTTCACACACCCCT | 68497 |
rs235544204 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84931673 | CAGCCCAGAGCCGAG[C/T]CTGCTCAGCACAAGG | 68497 |
rs235679233 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84921469 | TGCTAGAATGAACTG[C/T]AATAGGCCAATGATT | 68497 |
rs235694074 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84924945 | AACTGTGAACAAAGT[C/T]CTGTTCACTAGCTAT | 68497 |
rs235709543 | in-del | -/G | | | intron-variant | Arel1 | Mm_Celera | 12:84922004 | GATTGCCCAGGGGAA[-/G]GGCCCTTTATGAGTG | 68497 |
rs235741217 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84924514 | CTCTATCACCCAAGT[A/G]CACAGATGGAAAGAG | 68497 |
rs235754717 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84929836 | TGCTTCTCCAACTAC[A/G]ACTTCTGCTCCCTAC | 68497 |
rs235785738 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84958088 | AGAGGCAGGTAAAAA[C/T]ACCATGCCAAAAAGG | 68497 |
rs235787929 | in-del | -/AC | | | intron-variant | Arel1 | Mm_Celera | 12:84934089 | AGAGTTTCCATTACT[-/AC]ACACTGGCCAGACTG | 68497 |
rs235822783 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84926756 | CTGTGGTTAAGTGAC[A/G]TGTTCTCTTTATAAG | 68497 |
rs235837091 | in-del | -/AG | | | intron-variant | Arel1 | Mm_Celera | 12:84955915 | GTAAAAAAAAAAAAA[-/AG]AATGCAGTTCTCCAA | 68497 |
rs235909173 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84935762 | AAAGAAAACTGATTT[A/T]AAAATACAGAATTTA | 68497 |
rs236032558 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84945732 | GAGAACTTTTGATTG[A/G]CTGTGGACAAGGGTA | 68497 |
rs236058478 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84938391 | ACTTGTATTTTATTC[A/G]TATGTGTGCTATGCC | 68497 |
rs236107300 | in-del | -/CCA | | | intron-variant | Arel1 | Mm_Celera | 12:84955880 | GTCACCTACTGGTTT[-/CCA]CCACAAAACAAGATG | 68497 |
rs236107694 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84953166 | CAACCATCTGTAATG[A/G]AATCTGATGCCCCCT | 68497 |
rs236157373 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84937067 | AGTGAAGAAATAGAG[C/T]CCAAATGCTACAGCC | 68497 |
rs236170604 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84962338 | TAGAACCCAGAACAC[A/G]TTCCTTGGGACAAAG | 68497 |
rs236174394 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84952486 | ACTGGAGGCCAGCAG[A/G]TCAAATAAGTTGGCA | 68497 |
rs236181077 | in-del | -/AA | | | intron-variant | Arel1 | Mm_Celera | 12:84966791 | AACAACAACAACAAC[-/AA]AAAAAAAACCAGGTA | 68497 |
rs236223879 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84935836 | TAATACCAGCACTTT[A/C]AAGGCAAAGGCAGGC | 68497 |
rs236296031 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84945604 | AGTGAGGTCTCAGAC[C/T]CCAGCAGAGAAGCTA | 68497 |
rs236360221 | snp | A/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948627 | TGCTCAGCTATTGGC[A/T]GAATCAGTTCTTTAT | 68497 |
rs236581534 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84925270 | ACTATTATCATTTGA[-/T]TATCACATAACTCCA | 68497 |
rs236753428 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84963860 | GAGTCCAGTTCCCGG[C/T]ACCCATGCCAGGTGG | 68497 |
rs236788501 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84957115 | TGGTTTCTCTGCACG[A/G]CATACTCTTCATTGT | 68497 |
rs236811403 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84967266 | AAGGCTAGAAGAAGG[C/T]GACAAACCCCCTGGA | 68497 |
rs236867234 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84965489 | AGCTCAACACTCACA[A/C]ACACACCCAAACCCC | 68497 |
rs236895418 | in-del | -/AAAAG | | | intron-variant | Arel1 | Mm_Celera | 12:84955912 | AATGTAAAAAAAAAA[-/AAAAG]AATGCAGTTCTCCAA | 68497 |
rs236940813 | snp | C/T | | | missense, nc-transcript-variant | Arel1 | Mm_Celera | 12:84921319 | TTGAAGTCAGATACA[C/T]TGATGTCTCCAGTCC | 68497 |
rs237032051 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84961599 | GGGAACTGAACTCAG[A/G]TCCCCTGGAAAAGCA | 68497 |
rs237087180 | in-del | -/TTTTG | | | intron-variant | Arel1 | Mm_Celera | 12:84941342 | TGCTGGGATTGAAAA[-/TTTTG]TTTTGTTTTGTTTTG | 68497 |
rs237095292 | snp | A/G | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84970109 | GTTAGAAAACAAGCC[A/G]GGGAGTAGTGGGCTT | 68497 |
rs237126580 | in-del | -/AC | | | intron-variant | Arel1 | Mm_Celera | 12:84921583 | CACACACACACACAC[-/AC]ACACACACACACATA | 68497 |
rs237168296 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84929262 | CACTGGGGTAACTTC[A/G]CCCTGGACAAAACAC | 68497 |
rs237258002 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84938675 | TCCCCTATCTCTTAT[C/T]TATCATGCATGAGAA | 68497 |
rs237307361 | in-del | -/TG | | | intron-variant | Arel1 | Mm_Celera | 12:84936474 | AACTCTCTCAACACA[-/TG]GTCCTTGGGCAACCA | 68497 |
rs237314534 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84932552 | GAGGCAGAGGCAGGC[A/G]GATGTCTGAGTTTGA | 68497 |
rs237367179 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84922630 | ATGATACTGACAATA[A/G]CGGTTTCCTTACACA | 68497 |
rs237399827 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84943281 | GATAGGGAGGCAAAC[A/G]GGAACTCGACAACAT | 68497 |
rs237408859 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84931059 | GTGCCTCCTGTCCTG[C/G]AGTGAGTGCTGGGGC | 68497 |
rs237485410 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84959358 | AGGATGTTATAAGGT[A/G]GGGGTGGTTGCTGGA | 68497 |
rs237626917 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84921856 | GAAGTTGGATTATAC[A/G]TTAATACAGCTGAAG | 68497 |
rs237655764 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84932965 | GCAAGATTTTTTTTT[-/A]AATCTGTTATGTAAA | 68497 |
rs237696020 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947455 | AACTTACAGAGTTCC[A/G]CCTGCCTCTGCCACC | 68497 |
rs237761483 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84946556 | CTGCAACCCCAGCCC[C/T]GTGGGGGCAAAACCA | 68497 |
rs237814621 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84928390 | CAGGCACAGCCTGGT[A/G]GGAGTAGCCAGCAGT | 68497 |
rs237824260 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84955004 | TCGTTCATATACCCA[A/G]TCTATACTCAGTTTT | 68497 |
rs237847485 | in-del | -/TTTGTGT | | | intron-variant | Arel1 | Mm_Celera | 12:84962758 | TGCTGTGTGTGTGTG[-/TTTGTGT]TGGGGCGGGGGGTGC | 68497 |
rs237949209 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84937147 | AACATCAACTGTCTT[A/G]GCAAACATCTTCCAG | 68497 |
rs237979714 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84919357 | AGATGCTATCTTCCT[C/G]GAGACTGAGAAGTTC | 68497 |
rs237996638 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84924238 | CAAGTTTCTCATCTG[C/T]ATTAGCCTTTTTAAC | 68497 |
rs238022665 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84946103 | ATTCTTCTGTGACGT[A/G]GACACTGGTAAAGTG | 68497 |
rs238201950 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84958703 | CATTGATAAAGCCAC[C/T]TATTTGATAGCTGAG | 68497 |
rs238218920 | snp | C/G | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948216 | GCCTAGAAAAGTTAA[C/G]CTGATGAGGCTCTCC | 68497 |
rs238242383 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84949420 | GGCTCACAACCATCT[C/G]TAATGGGATCCAATG | 68497 |
rs238280327 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84957404 | CTTTGGTTTTTTTCT[A/C]AAGTGCCTTAACCAT | 68497 |
rs238292597 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84940459 | GAGAACCACTTCCCA[C/T]GTGGCCAGGGTGTGG | 68497 |
rs238324870 | in-del | -/C | | | intron-variant | Arel1 | Mm_Celera | 12:84945923 | GTTGGCCAGACGTGG[-/C]AGGGCTGCCACACTT | 68497 |
rs238370079 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947868 | AGTAACTCATGGGTA[C/T]GTACACCTGCAGCCA | 68497 |
rs238374986 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84940563 | GTCTTAGAAACACAG[C/G]GAGAGACATGTTTAT | 68497 |
rs238436037 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84939195 | GGTTTGGGCCAAGGT[G/T]CTTTTACTTAAAAAG | 68497 |
rs238443543 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84944080 | GTACATCAGCATCCC[A/G]CACTCAGAGACTAGA | 68497 |
rs238504651 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84951561 | AAGCTTTCCAACACA[A/C]ACGTCATAGTTCTGC | 68497 |
rs238534643 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84953553 | CTCAGAACCTCTGCT[C/T]GCTCTGGCCCTGCTT | 68497 |
rs238594008 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84963384 | CGTGGACCTGGCCTG[A/G]CATTCTTCATCACTA | 68497 |
rs238639329 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84942696 | CAGGACAAACCCCAC[C/T]CTGGTGTTACACCTC | 68497 |
rs238709483 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84945669 | TTAAACTCCTTCTAA[A/G]GAATGTTTACAGTCA | 68497 |
rs238724595 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947254 | AGGGAACAACCTGTC[-/TT]TTAGATACAGCTTAG | 68497 |
rs238766762 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84927066 | TTTTTCTTTGGATAA[C/T]AGCTTAATTACTATA | 68497 |
rs238831719 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Arel1 | Mm_Celera | 12:84926276 | TTGGGCCAGGAAAGA[C/T]CGAGTGAACCGGGCA | 68497 |
rs238918461 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84966515 | TTCAAAGGTAAAATG[A/T]GGGCCTCTGGCTATA | 68497 |
rs238962505 | snp | A/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971807 | CAGAACCTTCGAACA[A/T]GCTAGTATGATATTC | 68497 |
rs239080261 | in-del | -/C | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969928 | ACGAAGAGCACTGTT[-/C]CCCCATCACATTCCA | 68497 |
rs239102855 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84964913 | CATGGCTTATATAGC[A/G]GTCACAGGACCGTTT | 68497 |
rs239130060 | in-del | -/CA | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84919742 | GACACGGCCCTTCCC[-/CA]CGAGAGAAGCGTACC | 68497 |
rs239166217 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84964262 | TTCTTTTATTTTTTT[A/G]AGCTCCTTTTTTTAT | 68497 |
rs239325649 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84960577 | TTACAGATTTATTTT[A/G]TGTATATGAGTGTTT | 68497 |
rs239326568 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84954626 | CTGTGTTCAGCTACT[G/T]GGTTATTATAACTAG | 68497 |
rs239527831 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84952320 | ACTTTACAGTCCAGA[A/C]GTAACGAGTAAGATA | 68497 |
rs239562669 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947308 | ATGGACACCAAGGCC[-/T]TGTACATCATCAAAA | 68497 |
rs239565740 | in-del | -/AAAAAAAAAGAAAAGAAAAAG | | | cds-indel | Arel1 | Mm_Celera | 12:84951149 | TTGCACATTTGAAAA[-/AAAAAAAAAGAAAAGAAAAAG]AAAAGGCCAAAAAGT | 68497 |
rs239586955 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84958380 | TCTAAAGGTCGCTGA[A/C]TTGCCAAATATGACT | 68497 |
rs239602000 | in-del | -/AC | | | intron-variant | Arel1 | Mm_Celera | 12:84921599 | CACACACACACACAT[-/AC]ACACACACACACACA | 68497 |
rs239676360 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84924817 | GCTTATTCACAAAAA[A/C]CATACCAAATTATAG | 68497 |
rs239683313 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84926921 | AGAACCTTAGATCTG[-/T]TTGTGGTCCTTAGTT | 68497 |
rs239794498 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84923794 | TATACCCGACTGGCA[C/T]CCGTGTGTCCTCACA | 68497 |
rs239794511 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84932992 | TAAATGTTATCATAC[A/C]CAGTTCCTTGTTTTA | 68497 |
rs239809054 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84949812 | CTACCTAGACCACCC[A/G]TGAGCATACCCTGAC | 68497 |
rs239811115 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84960947 | ATTATGGATAAAGTC[A/G]CAATGACCCTTCAGG | 68497 |
rs239816382 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84924776 | TTAAGGACCTAATAA[A/C]ATTTTCTTAGGCCAT | 68497 |
rs239864604 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84921824 | ATGAGTACACTAGGT[A/C]CTGAAGCAGAATCTC | 68497 |
rs239876469 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84960101 | GATAGCTCACAGCCA[C/T]CTGTAACTCCAATTC | 68497 |
rs240027081 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84923552 | GTCTTTCTGGCTACA[C/G]AGTGAGACTGTCTCA | 68497 |
rs240055145 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84968468 | TAATCTCCCACCCCC[-/A]AAAAACGGCTAAATG | 68497 |
rs240076014 | in-del | -/CTA | | | intron-variant | Arel1 | Mm_Celera | 12:84938855 | GGCCAGTTTCCTTTG[-/CTA]CTCTAGAAAAAGAGA | 68497 |
rs240083852 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84926939 | GTGGTCCTTAGTTGA[C/T]TTGAGTACAGGTGAT | 68497 |
rs240090509 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84922888 | AAATGGTGTTTAGCC[A/G]GGCGGTGGTGGCACA | 68497 |
rs240186476 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84923387 | GATAAATATTAATGA[C/T]TACTCTTCATAACTA | 68497 |
rs240249437 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84962427 | CCTGTCTAGTTTAAG[C/T]GTCACTCTGGCCTAT | 68497 |
rs240263704 | in-del | -/AA | | | intron-variant | Arel1 | Mm_Celera | 12:84937114 | AGCAATTTCTTTCTT[-/AA]AAAAAAAATAAAAAT | 68497 |
rs240307865 | in-del | -/CCAG | | | intron-variant | Arel1 | Mm_Celera | 12:84946034 | TGAACTCACAAGGCC[-/CCAG]CCCTTACTGAGGATT | 68497 |
rs240316157 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961856 | GTTACAGGTGTGACG[C/T]GCCTGACAAGGTAGT | 68497 |
rs240378187 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Fcf1, Arel1 | GRCm38.p3 | 12:84970752 | GGTCCGAGGAAGCAG[A/C]GGCCTCATCCAGCAC | 68497 |
rs240612586 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84964616 | TCCTGACAAGCCGCC[-/T]CCCTCCACAAGTCTA | 68497 |
rs240612594 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84942808 | CGTATGTTTGCAAAA[C/G]GAGGAATGTATTTGT | 68497 |
rs240613146 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84944623 | GAGAGTACTCACAGG[C/T]ACCTCACTTGGGTGT | 68497 |
rs240626038 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84954442 | CAGAGGCAGGCGGAT[C/T]TCTGAGTTCAAGGTC | 68497 |
rs240661057 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84966770 | TACACTAGACCTTTT[C/T]TTTAAAAACAACAAC | 68497 |
rs240676937 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84949647 | CACAGTCTATTAGCT[C/T]GGTGTGGAGATCAGG | 68497 |
rs240695316 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84952254 | CCTTCAGGATTTCCA[A/G]TGCATATACAGTTCT | 68497 |
rs240735893 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84949036 | CTTTTTTGTTATCTT[C/T]TGAAGTAAAAATAAC | 68497 |
rs240795951 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84964585 | CAGCAGGAATATTTC[-/A]AAAGCAAAACTCTGA | 68497 |
rs240814361 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84970944 | GCGATTCCGGAAGAA[A/G]CAGGAGTGCGGCGTG | 68497 |
rs240823480 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84931101 | CACCTGCCCTTTTAC[A/G]TGGGTTCTGGGGATC | 68497 |
rs240876319 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84941368 | TTTTGAGCCAGAGTC[C/G]CATATAGTTTAGAAT | 68497 |
rs241055481 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84933046 | CCTTAGACATGTTCT[A/G]CCTTGAACTACATCT | 68497 |
rs241057291 | in-del | -/ACAA | | | intron-variant | Arel1 | Mm_Celera | 12:84933736 | GAGGACTAGAAAAAC[-/ACAA]ACAGTCAAAAAGCCT | 68497 |
rs241136833 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84968057 | AAAATAAAAGAAAAA[A/G]AAAAAAAAACAGATT | 68497 |
rs241150701 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84943466 | AAAGCAGAGCACGTG[C/T]CGTAAGCCTACCAGC | 68497 |
rs241271903 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84960020 | TAAGGCATGGCTGGA[C/G]AGATGATTCAGCCTT | 68497 |
rs241293647 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84935299 | AGCTGCAGTCCCTCA[A/G]AGAGCCTGGAGGAGC | 68497 |
rs241408133 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84935343 | GCACTCAGAAGGCAG[A/G]GGCAGGTGGATCTCT | 68497 |
rs241422210 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84932503 | AAATACCGTCCGGGC[-/A]GTGGTGGCGCACACC | 68497 |
rs241481764 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971416 | TAGAAACATTTGATG[-/T]TTTTTTTGTTTTGCT | 68497 |
rs241650794 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84932887 | AATATCTTACCATGA[C/T]AAATTAGTTATCTAA | 68497 |
rs241657300 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84928307 | GAGCAAGCAAGTGGT[A/G]GGGAGATGGAAGAGA | 68497 |
rs241708201 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961900 | CAAGAACAGTAAGTG[C/T]TCTTAACCACCGAGT | 68497 |
rs241786709 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84936420 | CACCCACCCACCCAG[A/C]TGACGAAGGTGCAAA | 68497 |
rs241830255 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84945752 | GGACAAGGGTAGCTA[C/T]ACTCATGGCTAGTCA | 68497 |
rs241836662 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84956073 | ATTTTTTTTCCCCAT[C/T]CCAAACCACACCATA | 68497 |
rs241915586 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84964880 | ATTCTCAGCGTGTGT[A/G]CATAGGTACGCATGG | 68497 |
rs241961445 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84959918 | GAACTATGAAGACCA[C/G]GCAGGCCTTAAACTC | 68497 |
rs241962139 | in-del | -/GAAGG | | | intron-variant | Arel1 | Mm_Celera | 12:84968050 | CGATTTAAAATAAAA[-/GAAGG]GAAAAAAAAAAAAAA | 68497 |
rs242033324 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84944261 | GAAAGTGCCTACCTG[C/T]CTCTGACAATTACAA | 68497 |
rs242127905 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84962661 | CAGTCTGGACCAGTG[C/T]ACTAATCACTCTTAG | 68497 |
rs242165404 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84928192 | CTCCATGTAGCCAGG[C/T]GGGCAGACCACACCT | 68497 |
rs242280725 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84923253 | CTGCAGTTTCTCTGG[A/T]ATCTCAGCACACAGC | 68497 |
rs242367854 | in-del | -/G | | | intron-variant | Arel1 | Mm_Celera | 12:84954138 | ACGAATATTAATTTT[-/G]GGAGACCTACTTTCT | 68497 |
rs242387265 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84925572 | CAGTTTAGGCACGGA[C/T]GCTGCATCAGCGTCA | 68497 |
rs242396789 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84921917 | CTAGTTAAGAACTGC[C/T]AAGGTGGCTTTGTCA | 68497 |
rs242463395 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84930332 | GCCCCCATGGCTCAC[C/T]GCCTTCCCACCCTTA | 68497 |
rs242464448 | snp | C/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972504 | TAGGAGGGCCACCAT[C/G]CCTACCTTGGGATAT | 68497 |
rs242501075 | in-del | -/TCTACAAGGATT | | | intron-variant | Arel1 | Mm_Celera | 12:84931138 | GGTGGTTGGGTTTGG[-/TCTACAAGGATT]TCTACCACTGAGCCA | 68497 |
rs242520229 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972078 | TTTCTCTGTATCGGT[A/G]AGGACTGGGTAAACA | 68497 |
rs242597526 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84944471 | TCTAAAGGCAGAGTG[G/T]AACAAATAGTGAAAC | 68497 |
rs242712526 | snp | A/T | | | utr-variant-5-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84951222 | AAATCTTCATTGAGG[A/T]TAAGTGTGTCCCAGG | 68497 |
rs243013380 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84952966 | GGGATCTGGTGTCTT[C/T]TGGCACCCATGGGTA | 68497 |
rs243106771 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84936035 | CACAGGTCCCTCACT[A/G]CTCCGTGTCCTCCTT | 68497 |
rs243128826 | in-del | -/G | | | intron-variant | Arel1 | Mm_Celera | 12:84940418 | ATGGAAGAGAGGGGT[-/G]GGCACCCATTAGTAC | 68497 |
rs243154782 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84963073 | TCTGGATTCTCCTGC[A/G]TCTACCACCCAAGGG | 68497 |
rs243341352 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84955635 | ATGTGTGCTTGGGGG[A/G]GATCAGAAGAGGGCA | 68497 |
rs243347618 | in-del | -/G | | | intron-variant | Arel1 | Mm_Celera | 12:84925840 | AGATAGGAAGACACA[-/G]AAGCACATGGACACC | 68497 |
rs243355460 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84919763 | AGAAGCGTACCCAGC[A/C]CTGGAGGCTGCAGCG | 68497 |
rs243502483 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947359 | CCTAACCCTAATACA[A/G]TGTTTGTTTGTTTTG | 68497 |
rs243687376 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84931303 | GTGATCTTTACAAAC[C/T]ACACATCCAGGTTAA | 68497 |
rs243753130 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84941395 | GAATGGGCTTTGAGA[C/T]CCCCATGTACACAGG | 68497 |
rs243811259 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84934108 | CTGGCCAGACTGGGC[A/G]GGGTGGTGGTGGTGG | 68497 |
rs243891414 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84944141 | AGAGCACAGAACAAT[C/T]TGAAAAGGGAAAGGA | 68497 |
rs243909768 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84964509 | AGGAGGACAGGGCCC[C/T]GTGTCCCCACCCCAC | 68497 |
rs243990503 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84919690 | AAGAACAATTCAGAG[A/G]AAAGCATCAGTAGTC | 68497 |
rs244049840 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84945892 | AGGCAAAGATGGAAG[A/G]AAGTGGTAGCATACT | 68497 |
rs244073585 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84927204 | TCATTACACACAGCA[C/T]ATGAAGAGCAAAGTT | 68497 |
rs244077658 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84965613 | GGAATTCTGGATTGG[A/G]TTCTGCACAGAAAAG | 68497 |
rs244102737 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84927530 | CACTACCTGTTTCTT[C/T]AATGCAGCTCACTTA | 68497 |
rs244107029 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84953622 | AAGTACACTGTAGCT[A/T]TCTTCAGACACGACC | 68497 |
rs244108571 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84945473 | TCATCATTTCTCCTC[G/T]GATTCCTGTTACCCA | 68497 |
rs244151051 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84936171 | ATGTTGAAACACAGG[C/T]TTAAGACAATTTTTA | 68497 |
rs244161662 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84926710 | CAAAAGCAAGAAGGC[C/T]GGCCAGCCATAAACG | 68497 |
rs244170367 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84952893 | TTGCAGAGGACCCAA[A/T]TTCCATTCCCTGCAC | 68497 |
rs244224437 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84964633 | CTCCACAAGTCTAGG[-/A]AGTTGTTATTTTATT | 68497 |
rs244337160 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84956058 | AATTTTACTCTTGGA[-/T]TTTTTTTTCCCCATC | 68497 |
rs244386827 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84967798 | AACCATGCTACCTTC[C/T]ATCCCTATCAAAGGA | 68497 |
rs244471065 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84962477 | CATTCCTCAGCAGTT[C/T]AATTAAAACTTAGCC | 68497 |
rs244528933 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84956580 | ACTTCTGAGTGGGCA[A/G]TCCCCCAAATCACAG | 68497 |
rs244545689 | snp | C/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972052 | AAAATAAATAAAGAA[C/T]ACTCAACCAGTTTCT | 68497 |
rs244576641 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84955285 | CAGGCTAGCCTGAAA[C/T]TCACCACCCTCCTGT | 68497 |
rs244759988 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84952830 | TATATAAAGACTTTA[C/G]AAGGATGGTGGGAGA | 68497 |
rs244794055 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948080 | AGGGCTGCTTTAGCA[C/T]TAAGAACTAAGCCAA | 68497 |
rs244812941 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84962534 | TAAGCAAGTCCACAT[C/T]CCTTAAGTCTCTTTA | 68497 |
rs244818150 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84964166 | AAGCTGCTTTGAACT[C/T]CTGATCCTCACGTCT | 68497 |
rs244884019 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84961937 | TGCAGCTCTGTCCTG[C/G]GTTCTATAGTTTTAA | 68497 |
rs245104690 | in-del | -/ACAA | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969811 | ATCCTAAAAGCAAAG[-/ACAA]ACAAGCAAACGGAAA | 68497 |
rs245128104 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84965669 | TATCCAAGTCTGTAG[C/T]TTAGTAAGAAATCAT | 68497 |
rs245209011 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84920657 | AAGAGACTCCCCCAC[A/C]AGGGATGCTTCGGGC | 68497 |
rs245266150 | in-del | -/GA | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84970338 | CGTACACACACACGG[-/GA]AGAGAGAGAGAGAGA | 68497 |
rs245269347 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84963517 | AGAATGGCACGATAT[A/C]ATGCTGCTTTAGCTT | 68497 |
rs245383416 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84929746 | GTGTTCCATTTCTAC[C/T]AGACCAGAGTAACAA | 68497 |
rs245465669 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84921522 | AAAAACAAAACAAAA[A/C]AAAACAAAAATCACA | 68497 |
rs245517669 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84929991 | AACAAATAGTCTCTA[A/G]TATGTTTCAAGGGAG | 68497 |
rs245576617 | in-del | -/AAAAAC | | | downstream-variant-500B | Arel1 | Mm_Celera | 12:84917868 | GTCTCGAAAAAAACA[-/AAAAAC]AAAAACAAAAAGACA | 68497 |
rs245681157 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84959360 | GATGTTATAAGGTAG[A/G]GGTGGTTGCTGGAGA | 68497 |
rs245733082 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972624 | ACAATAGATATCATT[A/G]TGTTATTTTTCAAGT | 68497 |
rs245736072 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84967247 | TGTATGTGGTTTTTT[G/T]GTGAAGGCTAGAAGA | 68497 |
rs245785615 | snp | C/T | | | downstream-variant-500B | Arel1 | Mm_Celera | 12:84917976 | GCTATCTACAGTGAG[C/T]AGTGTGACCCTTAGG | 68497 |
rs245847863 | in-del | -/GA | | | intron-variant | Arel1 | Mm_Celera | 12:84922144 | GGAAAGAGAGAGGGG[-/GA]GAGAGAGAGAGAGAG | 68497 |
rs245884267 | snp | A/C/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84931497 | GACAGAATACACTGG[A/C/G]AACACATTCTGAACT | 68497 |
rs245924340 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948657 | TTGAACCAATCAGGG[A/G]GTAAGAGAGGGCATG | 68497 |
rs245943952 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84930862 | GGCTTGGCTGGCACA[C/T]TTAGCTGCTGAGCCA | 68497 |
rs245983828 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84957848 | GAGAGCTCGTTGCTA[C/T]GTAGAGAGGATCTGA | 68497 |
rs245995959 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84941135 | AGAAACTGGGCTGGC[G/T]TGGGCTTTCCGGCTC | 68497 |
rs246124533 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84929880 | GGAACTAATCAGCAC[C/T]GACCAGAGACCTGAT | 68497 |
rs246180511 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84928701 | CAGCAACCACATGGT[A/G]GCTTACAATCACCTG | 68497 |
rs246232380 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84938344 | TACAATGCCAGAAAT[A/G]TTTGTGTCCTTTAAA | 68497 |
rs246272948 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84942867 | GACCCTGTTGTCTAT[C/T]ACGAAGCCCAGGCAC | 68497 |
rs246285382 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84961108 | TTTACATTTAGAGCA[A/G]CACATGAGTCCGGTC | 68497 |
rs246294923 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84937073 | GAAATAGAGTCCAAA[C/T]GCTACAGCCACTCTG | 68497 |
rs246304169 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84937493 | CTTGAGCTCCTGGTC[C/T]CCCTGCCTCTACCTC | 68497 |
rs246564520 | in-del | -/AC | | | intron-variant | Arel1 | Mm_Celera | 12:84933740 | ACTAGAAAAACACAA[-/AC]AGTCAAAAAGCCTCT | 68497 |
rs246604041 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84944425 | ACCTCCTTAGCATAA[C/T]TCTGGCATAGTTCAT | 68497 |
rs246607559 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84941050 | GGTAAGGCTAGCTTA[A/G]TCTACATAGTGTGTT | 68497 |
rs246635485 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84957679 | CGCGATTCACTGTGG[A/G]AAGTGGACAATTACA | 68497 |
rs246636267 | in-del | -/C | | | intron-variant | Arel1 | Mm_Celera | 12:84936000 | CCACACACACCCAAT[-/C]CCCATCTGCCCATCT | 68497 |
rs246657640 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84939917 | GGTGATACCTGCTGC[A/G]CAATGAATTTTAAAA | 68497 |
rs246668050 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84951972 | TGGCATGGTAGTATG[A/T]GCCTGTGATCCCAGC | 68497 |
rs246668378 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948251 | AAAGTGATTCTTGGG[A/G]ATTTTCTCTGCCCCT | 68497 |
rs246702943 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84965885 | CTTGCATTTCCTTCC[A/T]TACCAAAATGTGAAA | 68497 |
rs246721370 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947675 | CTACTTTCTGTTGGC[C/T]CCACTTTCATACAAA | 68497 |
rs246764071 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84965320 | TGTTTGGTTAGTCTA[C/T]GGGGAGGAAAGGCAG | 68497 |
rs246898078 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84965017 | ACTTTCAACCTGATG[C/T]GCTGTGTTGCTGGCC | 68497 |
rs246939092 | in-del | -/ATAC | | | intron-variant | Arel1 | Mm_Celera | 12:84946348 | TCTAGATTTATATAT[-/ATAC]AACTTTTAAAAATTT | 68497 |
rs246955985 | in-del | -/G | | | intron-variant | Arel1 | Mm_Celera | 12:84949854 | TCCTCAAAGTAGAAA[-/G]GGCCCCTCTATATTG | 68497 |
rs247001767 | in-del | -/C | | | intron-variant | Arel1 | Mm_Celera | 12:84923290 | TCACACACCCCTAAA[-/C]AAATATACTCTATAA | 68497 |
rs247013460 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84931878 | TCTATATTTTCATAA[C/T]AAGAGGATACTTTAG | 68497 |
rs247069883 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84967038 | TGTCTGGGACAGAAT[A/G]GCCTCTCAATAAATG | 68497 |
rs247191765 | in-del | -/AG | | | intron-variant | Arel1 | Mm_Celera | 12:84926111 | AACACACATACACAC[-/AG]AATACAAATAAATCT | 68497 |
rs247263247 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84933230 | CCAAGTGCTGGGGTT[-/A]AAGGCGTGCACCACC | 68497 |