SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6238463 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ahctf1 | Mm_Celera | 1:179775618 | AGAAATCACTAAAGT[A/C]AAAATTAGATAAGTG | 226747 |
rs6290121 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179751558 | AATGCTTAGTTCCAG[A/G]TTCACTTTGGCTTCC | 226747 |
rs6290143 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179751576 | CACTTTGGCTTCCAC[A/G]GAGGCTAATGAGCCT | 226747 |
rs6290155 | snp | C/T | 0.5 | 0 | intron-variant | Ahctf1 | Mm_Celera | 1:179751585 | TTCCACNGAGGCTAA[C/T]GAGCCTGCTCTAACA | 226747 |
rs6290746 | snp | C/T | 0.5 | 0 | intron-variant | Ahctf1 | Mm_Celera | 1:179751690 | cagagtcttgccaca[C/T]agcccaaggtggcct | 226747 |
rs6354974 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179760844 | CCTGGGCAAGTCTGC[A/T]CTGCATGCAGTTCCG | 226747 |
rs6356510 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179761139 | GCAAAGTCTCAAATG[C/T]CCCAGAATAGTTTTT | 226747 |
rs6357059 | snp | A/C | 0.5 | 0 | intron-variant | Ahctf1 | Mm_Celera | 1:179761295 | ccacgtaagctacat[A/C]canccccAGTCAGAT | 226747 |
rs6357062 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179761298 | CGTAAGCTACATCCA[C/T]CCCCAGTCAGATGAG | 226747 |
rs13471301 | snp | A/T | 0.244898 | 0.249948 | missense | Ahctf1 | GRCm38.p3 | 1:179748643 | GAATTGGTGTCAGAT[A/T]TATCTTCTCAGTTTG | 226747 |
rs13471302 | snp | C/T | | | synonymous-codon | Ahctf1 | Mm_Celera | 1:179752519 | AAAAGATCCATCAGC[C/T]GCAGTCTCAGACCTG | 226747 |
rs13471303 | snp | C/T | 0.297521 | 0.245442 | missense | Ahctf1 | Mm_Celera | 1:179752565 | TGACATCTAAGAGGA[C/T]ACCTACAAAGAAGTC | 226747 |
rs30462187 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179772360 | AGAGTGCTCATCTAT[C/T]TAGTATGCACCAGCC | 226747 |
rs30467541 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179756222 | GGCATTTGTGAATGA[C/T]GCAAAACATGATAAC | 226747 |
rs30552463 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179767413 | TGTTGGAAACAACTA[C/T]AGCTAATGGAAAAGA | 226747 |
rs30566728 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179756598 | GCAGATAGCATTAGC[A/T]CTAGAGTAGCTGCCA | 226747 |
rs30603659 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179773949 | TACAATGGCTATCAA[C/T]CACTACCACCATCTG | 226747 |
rs30651778 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179790903 | CCACTGCTAGTGACA[A/T]CATGGCTCTTATCTT | 226747 |
rs30698227 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179756573 | TGATGATGTCATGAT[A/C]GTTACAATAGCAGAT | 226747 |
rs30752204 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179785368 | TATGTGTGTGGCTGA[C/T]TGCCAACTAAAAGGT | 226747 |
rs30764981 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179790600 | CAGGATAAAATCATA[C/T]CATACTAGCTATCAC | 226747 |
rs30853128 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Ahctf1 | Mm_Celera | 1:179759060 | AGCAAAAAATATTTG[A/G]CTGAGTTGACAAAGA | 226747 |
rs30904605 | snp | C/T | 0.48 | 0.0979796 | missense, downstream-variant-500B | Ahctf1 | GRCm38.p3 | 1:179753456 | GAAACCATGTCATCA[C/T]TCTGGCTGGTATTTA | 226747 |
rs30935257 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Ahctf1 | Mm_Celera | 1:179755842 | ACTCTTACTCTGTAT[A/G]CGTTCAACAATGTGT | 226747 |
rs30948345 | snp | A/G | 0.48 | 0.0979796 | synonymous-codon, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179753818 | AGGTGCTGCAGAGTC[A/G]CTTGCCTCAGCTTCT | 226747 |
rs31028142 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179771113 | TCTGGGCACCCCACC[A/G]CTACCCCCAACCCCA | 226747 |
rs31093006 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179774880 | AATATTCAGTATACA[A/G]CAATAGAGGAAGGCA | 226747 |
rs31109591 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179757518 | TTTGCTCTTTCATGT[C/T]CCAAAAGAAAGTATG | 226747 |
rs31147130 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179760609 | TAGCATTAATTTCAC[A/G]CTTAGCTCAGAAGAA | 226747 |
rs31283404 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179767711 | GTGAGTATGAGTACA[A/G]TTCAGGCACCCAGTG | 226747 |
rs31311753 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179776923 | CTGGCCTGCAAGGCA[A/G]TAGAATCCAGATCTT | 226747 |
rs31347114 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179770386 | TTCTCCGTGACTGAA[C/T]CTATCTGATATAATG | 226747 |
rs31351677 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179771165 | ATAGCTTTTGCTGTT[C/G]TGGAATCCACTCTAG | 226747 |
rs31382745 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179760785 | ATTACTAGCGACTAT[C/T]TAAGTATTTTAGTGG | 226747 |
rs31384542 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179795975 | TTATTACATAAACTA[A/C]TGTAAATCCCTCCTG | 226747 |
rs31418801 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179771443 | ACTTAGCATGAACAG[A/T]ACACTGGACCAAAAT | 226747 |
rs31434005 | snp | A/G | 0.5 | 0 | intron-variant | Ahctf1 | Mm_Celera | 1:179762015 | ACTTAGACAATCCCC[A/G]TCATTGAAAAATAGC | 226747 |
rs31452862 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179747822 | CCTCCATCCCTATAT[C/T]GACAGAGGCACTTGG | 226747 |
rs31473274 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179755719 | ATTCCAGACAAAAAG[C/T]TAGATTCATATAACT | 226747 |
rs31488960 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179760528 | CTTCTCCCTTTTGGC[A/G]GGTCTAACAGGACTC | 226747 |
rs31518140 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179761921 | AGCAAGTACTCTATC[C/T]GTGCATTACTGCTGA | 226747 |
rs31523974 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ahctf1 | Mm_Celera | 1:179758319 | AGTATATAAATTACA[C/T]GTCAGGCATTTTACA | 226747 |
rs31552749 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179773879 | GGGAAAACTACACAT[C/T]TTAGATAAAGAAGGG | 226747 |
rs31564574 | snp | C/G | 0.455 | 0.143091 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179771691 | TGGCAGTTACAGTCT[C/G]TCTGTGTCGATTCGA | 226747 |
rs31612611 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179762393 | AAGAAGGCAAGCCAC[G/T]TTCATAAGCTGACAT | 226747 |
rs31647853 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179764706 | TAATGTGGAAAAAAA[A/C]CAAAAACCAAAACCA | 226747 |
rs31659605 | snp | G/T | 0.375 | 0.216506 | missense, downstream-variant-500B | Ahctf1 | GRCm38.p3 | 1:179753463 | TGTCATCATTCTGGC[G/T]GGTATTTACAGTCTC | 226747 |
rs31722991 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179756108 | CAATCATCCAAATAG[A/G]TACAGATGTTTTCTC | 226747 |
rs31797886 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179762350 | CATACAAGCTGTCAT[C/T]AAATCTTACCTGCTT | 226747 |
rs31817540 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179749042 | ATCCCATGTGGCCTG[C/T]GAGTCTCCATTTCTA | 226747 |
rs31902175 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179764831 | GAAGGTTACAAATTC[A/G/T]AGGCCACTCTGAGCT | 226747 |
rs31902182 | snp | A/T | 0.487535 | 0.077957 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179760638 | AACACAAATCATGTT[A/T]AGAGGTTGAGATTTC | 226747 |
rs31903135 | snp | C/T | 0.432133 | 0.171253 | missense, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179762572 | TCACGGGTGAAGGAG[C/T]ACCTTCTGACTTAAA | 226747 |
rs31928546 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179775160 | CTTGGTGAAAGGCAC[C/T]ATGTATTTGTCTTAT | 226747 |
rs31929290 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179757624 | CTGCTCCGTCCCCTC[A/T]CCCTTCCCCTGCCCT | 226747 |
rs31971334 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179794892 | AATATGCACACACAC[A/C]CCCCAAACAAAATGT | 226747 |
rs32011260 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179765239 | TACCAGTCACTACCA[G/T]TTTGGGTTTGTTTTC | 226747 |
rs32014292 | snp | A/C | 0.487535 | 0.077957 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179767323 | ACCTGAAACCCTTAG[A/C]AGCTGTCTCCAGAGT | 226747 |
rs32020851 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179785441 | TTGTATTATTTCTCA[A/G]AAGAAACAAGAAGAA | 226747 |
rs32034146 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179760838 | AGTAGGCCTGGGCAA[C/G]TCTGCACTGCATGCA | 226747 |
rs32044532 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179780746 | GTGAGGCAATGAAGA[C/T]ACAAAAACTAGAATG | 226747 |
rs32046816 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179792760 | GTCCTCTGACCCTCA[A/C]ATGTACACCATGACA | 226747 |
rs32078279 | snp | A/G | 0.32 | 0.24 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179802429 | TTCTAAAGAATCCAC[A/G]CTCTTTAAAAAATGT | 226747 |
rs32090783 | snp | C/T | 0.48 | 0.0979796 | downstream-variant-500B, intron-variant | Ahctf1, Gm1305 | GRCm38.p3 | 1:179744594 | CACATGTGGCAAGAC[C/T]TACTTTTAAGATAAA | 226747 |
rs32099146 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179761865 | TATCCAGAACAGCTA[A/C]GTGTCTGTCAATACA | 226747 |
rs32123384 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179756351 | GAGATGATTTTCACC[C/T]GTGTTTGCCACCATA | 226747 |
rs32156895 | snp | C/T | 0.32 | 0.24 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179798693 | TGCACCACCACCACC[C/T]GGCCCCTTATGAGTT | 226747 |
rs32173950 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179797326 | TTTTATTCTCAGCTA[C/T]ACAAACTACCTACTT | 226747 |
rs32179725 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179774323 | TTAGGTTCATCAGGC[A/G]TGCACGACAGACACT | 226747 |
rs32208066 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179771211 | CTATGTAGACAAGGC[C/T]GCCCTTGGACTTGAG | 226747 |
rs32223507 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179764666 | AGACGGAACCTCTTC[A/T]CCTCAAACCAATAAA | 226747 |
rs32226370 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179772236 | TTTACTCTTGCTTAA[C/T]TATGAAAACTAAAAT | 226747 |
rs32226935 | snp | A/G | 0.32 | 0.24 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179762461 | TTATTTAGTCTTGAC[A/G]TTTTACTATGGTAGG | 226747 |
rs32230434 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179757642 | CTTCCCCTGCCCTTC[C/T]CCACTCTCTCCAACA | 226747 |
rs32243143 | snp | A/G | 0.32 | 0.24 | intron-variant | Ahctf1 | Mm_Celera | 1:179771734 | CCCAGAGACTCATGG[A/G]CTAACATGTGCTCAC | 226747 |
rs32262309 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179770772 | GACCCTACATTTCTT[C/T]TGAAGTTCATACTGG | 226747 |
rs32266872 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179761883 | GTCTGTCAATACAGC[A/C]CACCACACTCTATAG | 226747 |
rs32302393 | snp | C/T | 0.484429 | 0.0868505 | missense, downstream-variant-500B | Ahctf1 | GRCm38.p3 | 1:179753483 | TTTACAGTCTCTGCA[C/T]GTGGTTCCTTAACAG | 226747 |
rs32315768 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179797507 | CCAGTCTCAGAAGGC[A/G]AAGACATTCAAATCT | 226747 |
rs32330734 | snp | A/C | 0.487535 | 0.077957 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179767267 | CACAGTTAATAGGAT[A/C]TGTCCTCTGAGTTAA | 226747 |
rs32363444 | snp | A/C | 0.487535 | 0.077957 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179790506 | AAATCTGGGTTAAGG[A/C]GAAACTGTTTTTACA | 226747 |
rs32375796 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179771148 | AGACAGGATCTCATT[C/G]TATAGCTTTTGCTGT | 226747 |
rs32382692 | snp | A/T | 0.487535 | 0.077957 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179784543 | ACACTGAGCTATATA[A/T]TCTCAGTCAGTCCTT | 226747 |
rs32400718 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179757177 | TCTGCAGCTCCTGTG[C/T]ATCAGTCTCAATCTT | 226747 |
rs32402518 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179796561 | AATTAAAAAAAATTA[A/T]GCATATATCCTAAAC | 226747 |
rs32407184 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179748077 | CTGGCAAGCACTTTA[A/G]TTTTAAACCTTGACT | 226747 |
rs32422936 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179770377 | CCTTTCATTTTCTCC[A/G]TGACTGAATCTATCT | 226747 |
rs32424340 | snp | C/T | 0.375 | 0.216506 | synonymous-codon, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179776029 | GTCATTATGATCTAG[C/T]AGCCAAAATCCTTGA | 226747 |
rs32425436 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179759348 | TGCTAGTGTATACTT[C/T]AAGGTAACCTTACAC | 226747 |
rs32439477 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Ahctf1 | Mm_Celera | 1:179764588 | AAACTATTTTCATAT[C/T]AGCATTTAGTGAAAT | 226747 |
rs32476239 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179772361 | GAGTGCTCATCTATT[C/T]AGTATGCACCAGCCT | 226747 |
rs32482229 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179756142 | TATGTCATAATTTTA[G/T]AGCCCAATTAAAAAG | 226747 |
rs32498434 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179771219 | ACAAGGCCGCCCTTG[A/G]ACTTGAGATCTGTCT | 226747 |
rs32498442 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179756136 | CTCAGATATGTCATA[A/G]TTTTATAGCCCAATT | 226747 |
rs32505334 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179755748 | CTCAAAAAGCAAAGA[A/C]TTACCTAGACTTAAA | 226747 |
rs32545224 | snp | C/T | 0.32 | 0.24 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179771735 | CCAGAGACTCATGGA[C/T]TAACATGTGCTCACC | 226747 |
rs32547688 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179765012 | AACCATATGGTGGCT[C/T]ACAACCACCCATAAT | 226747 |
rs32553084 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179760593 | TAGGTGAAAAAACCC[A/G]TAGCATTAATTTCAC | 226747 |
rs32572812 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179748988 | CACAAAGCTACTGAA[C/T]ATTAGTTTGACCCTC | 226747 |
rs32575544 | snp | A/G | 0.484429 | 0.0868505 | missense, downstream-variant-500B | Ahctf1 | GRCm38.p3 | 1:179753544 | AATGTGCAGCCTTTG[A/G]GACTATCACTGCTCC | 226747 |
rs32583582 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179757245 | CACTGTGACAGGGCA[A/T]AAAGTTTAATAGTGG | 226747 |
rs32607388 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179767018 | TTTGATTAAGAAATG[G/T]TATATAAAGGAAATG | 226747 |
rs32628969 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ahctf1 | Mm_Celera | 1:179765098 | TAGTAAATAAATCTT[A/T]AAAAAAAACAAAAAA | 226747 |
rs32629277 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179757630 | CGTCCCCTCTCCCTT[C/T]CCCTGCCCTTCCCCA | 226747 |
rs32641699 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ahctf1 | Mm_Celera | 1:179761989 | TGATTTTCTACTAGC[A/G]CACATAAAATACTTA | 226747 |
rs32648254 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179777140 | CAGCTCGCTCCCAGC[A/T]GTATTCTGAGTAGCT | 226747 |
rs32648257 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179777211 | CTGGGCCACCACTCA[C/T]GCACTGACTCCTCTC | 226747 |
rs32648260 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179777684 | CTGTCAATGGCTCCG[A/T]GTCACTGTGACCTAC | 226747 |
rs32648263 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Ahctf1 | Mm_Celera | 1:179777872 | TCAATGTTAACTGTT[A/C]ATAACAAAACAGGAA | 226747 |
rs32648885 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179777934 | AAGACAGGTGAAAAC[A/G]GGCTTCATTTAGTAT | 226747 |
rs32648888 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Ahctf1 | Mm_Celera | 1:179777963 | ATCACGGGACTGTAG[A/C]GCTCAAAGGAGCATT | 226747 |
rs32648891 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179777994 | AGTTAGAAAAAAATC[C/T]CTAAGTTGCCTTAAG | 226747 |
rs32649509 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B, intron-variant | Ahctf1, Gm1305 | Mm_Celera | 1:179744851 | CACCGCACATCTCTA[C/T]TTAGCAAACTGCACT | 226747 |
rs32649512 | snp | A/T | 0.497778 | 0.0332592 | utr-variant-3-prime, intron-variant | Ahctf1, Gm1305 | GRCm38.p3 | 1:179744980 | TTAGAGCTTTTGTGA[A/T]TCATTTGACAAATCC | 226747 |
rs32649694 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179778074 | CAAAACGGCTGACTG[C/T]TCTATTTTCCACCAT | 226747 |
rs32649697 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179778408 | TTAACAGCTACCAAC[A/G]TTTAGAATATGCATG | 226747 |
rs32649700 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Ahctf1 | Mm_Celera | 1:179778459 | TAGCACATTAAAGAC[G/T]GAGGTAGGAGAATCA | 226747 |
rs32649703 | snp | C/T | 0.32 | 0.24 | intron-variant | Ahctf1 | Mm_Celera | 1:179778521 | GAACACCCTGAGCAA[C/T]TTACTGTTTCAAGAT | 226747 |
rs32650415 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179778651 | CATTCAGTGTATTAG[C/T]ATTACAGGGCATTCC | 226747 |
rs32650417 | snp | A/G | 0.32 | 0.24 | intron-variant | Ahctf1 | Mm_Celera | 1:179779570 | ACAATACTTGACTAC[A/G]TGAGAATGAATATTG | 226747 |
rs32650420 | snp | A/T | 0.32 | 0.24 | intron-variant | Ahctf1 | Mm_Celera | 1:179779783 | CTGACTTTACTGTAA[A/T]TGTTTAATAAATTTT | 226747 |
rs32650423 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179780190 | AACTTTCTGTGCTTC[C/T]CAGAAATACACGGAG | 226747 |
rs32650545 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, synonymous-codon | Ahctf1, Gm1305 | Mm_Celera | 1:179745126 | ACTGACCTGGCTGAA[C/T]GGCCGCACCCGGACG | 226747 |
rs32650548 | snp | C/T | 0.401235 | 0.199068 | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | GRCm38.p3 | 1:179745390 | TTCCATCAGGCGCCA[C/T]TACCAACGGTACACA | 226747 |
rs32650551 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179745671 | AGGAAGCAGTGAAAC[C/T]GGTCAATCTAACCTG | 226747 |
rs32651216 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179780289 | ACATTACTAGACTAA[A/C]AGAAACACTTAATTG | 226747 |
rs32651219 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179780776 | GAAGACTAGTCAACA[C/T]AGTGTAAAGGCTCAG | 226747 |
rs32651221 | snp | C/T | 0.415225 | 0.187619 | synonymous-codon, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179780875 | GCCTTCGGGCAGAAG[C/T]CCCGAGTGGCAGAAC | 226747 |
rs32651284 | snp | G/T | 0.231111 | 0.249285 | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | GRCm38.p3 | 1:179745777 | GCAGTACTGGAAAAT[G/T]ACTCATTTGAGGTAG | 226747 |
rs32651287 | snp | C/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179746891 | AAGCACAGCCTGAGA[C/G]TCCTGCTACACAAAG | 226747 |
rs32651290 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179747120 | GAGAAGTGGTCTCAC[C/T]CTTTCTAGCACCCTC | 226747 |
rs32651293 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179747137 | TTTCTAGCACCCTCT[C/T]GGCTCCAGGGGATGA | 226747 |
rs32652026 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Ahctf1 | Mm_Celera | 1:179747763 | TTTCCACAGAAACTA[C/T]TCAAAGCCTACACCA | 226747 |
rs32652031 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Ahctf1 | Mm_Celera | 1:179748136 | CCCTGTCTTAAAGAC[A/C]GCAAACACAGGGTTG | 226747 |
rs32652204 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ahctf1 | Mm_Celera | 1:179781020 | AATCATGAACAACAA[C/T]CAAAATAATCAACAG | 226747 |
rs32652206 | snp | C/G/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179781761 | GTCAATAAAACGACA[C/G/T]GAACCGTCAAACAGC | 226747 |
rs32652209 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179781823 | GTTTCAACACAGTAA[C/T]TTACAATCAATGTGC | 226747 |
rs32652212 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179781847 | AATGTGCATTTTTCT[G/T]AAGTCCCATTACTCT | 226747 |
rs32652305 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179783325 | CCAAAACAGTCCAAA[C/T]CAACAACAAAAAAGG | 226747 |
rs32652554 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Ahctf1 | Mm_Celera | 1:179756744 | CCTGTGCAGCTTGTA[A/G]TCACCTACTATCTTC | 226747 |
rs32652557 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Ahctf1 | Mm_Celera | 1:179756850 | GTTTTACTTTACATG[A/T]TGAGAATCTTCCCTA | 226747 |
rs32652563 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ahctf1 | Mm_Celera | 1:179757298 | AAATGCCATCAAAGT[A/G]CAGTGCTAAGATTAA | 226747 |
rs32652576 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179770409 | ATATAATGGTAAATG[A/C]AGAAAATGTAAGTAG | 226747 |
rs32652579 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179770488 | TCAGGACAATGTAAA[C/G]TAAGATGGTTATGAG | 226747 |
rs32652583 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179771641 | AGTGCTTCTTACTTA[A/G]GTGTCCTGGCGTCAG | 226747 |
rs32652754 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ahctf1 | Mm_Celera | 1:179748422 | TTAGGGAAAAAAAAT[C/T]GCTTAAACATCCTTT | 226747 |
rs32652758 | snp | C/T | 0.260355 | 0.249785 | missense | Ahctf1 | GRCm38.p3 | 1:179748673 | CTTTCAGCTGGGCTG[C/T]GGCCTCCATGTTCTC | 226747 |
rs32652763 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ahctf1 | Mm_Celera | 1:179749072 | AGATGAGGTTTTCAT[C/T]ACACTGTGAATTTTA | 226747 |
rs32652884 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179801163 | TCAGACAGGATTTCT[A/G]AACTCCTGGCCTTAA | 226747 |
rs32652886 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179801362 | ATAAGATGCAGGAAT[A/G]AAAGCTACAATAGAG | 226747 |
rs32652889 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179801566 | GATTTGAAATGTGAG[A/G]ATTTTAAAACGTTAA | 226747 |
rs32652890 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179801605 | GCCTCAAAAGATGAG[C/T]ACCCAACATTAAACA | 226747 |
rs32652893 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179801629 | TTAAACACCTTTTCA[A/C]GAATATTATGAGCCC | 226747 |
rs32652914 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Ahctf1 | Mm_Celera | 1:179750626 | CAATGCAAGTCTATA[G/T]TCACAACTCTCTAGG | 226747 |
rs32652917 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Ahctf1 | Mm_Celera | 1:179750711 | GTTAAGCTTCCACAT[G/T]TACTTTTAAGACTAA | 226747 |
rs32652920 | snp | C/G | 0.426035 | 0.177515 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179750949 | GGTTTCTTTAACACA[C/G]CTCTTTTAGGGCAGA | 226747 |
rs32652922 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ahctf1 | Mm_Celera | 1:179751144 | CTTTTTGTGGTCAAA[C/T]GACTCCACTGTGGTC | 226747 |
rs32653055 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179782645 | ACTGCTGAGATTACC[A/G]ACACCTAACCTTGTC | 226747 |
rs32653057 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179783256 | GGAGCAGTTATGAGG[A/G]AGAGCAATATATACA | 226747 |
rs32653060 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179783402 | AATATTTAAAAGACC[A/C]CAAATCATGGTAGGC | 226747 |
rs32653062 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179783717 | TTGAAATGATTAAGA[A/T]ACAGGAAGCTTTCTT | 226747 |
rs32653063 | snp | A/G | 0.32 | 0.24 | intron-variant | Ahctf1 | Mm_Celera | 1:179783887 | ACGTGAATTTAAAAC[A/G]ATCTCATGCATAAAG | 226747 |
rs32653436 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ahctf1 | Mm_Celera | 1:179757386 | TCTAACTGTGAACCC[A/G]CAGAATAAAAATACC | 226747 |
rs32653441 | snp | A/G | 0.375 | 0.216506 | missense, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179757955 | TTGTGGTCTGCTGTA[A/G]GTATGGAGGTTCGGC | 226747 |
rs32653443 | snp | C/T | 0.152778 | 0.230321 | synonymous-codon, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179757993 | AGGCACGATTCCATC[C/T]AGAACTGACGTCTTG | 226747 |
rs32653678 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179773245 | GTGCACCATGTACAT[A/G]AAGAAGCCAGTGGAG | 226747 |
rs32653679 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179773364 | CTCTTCCTAGTAACT[C/T]ATCAAATAGAACAGG | 226747 |
rs32653681 | snp | G/T | 0.426035 | 0.177515 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179773378 | TCATCAAATAGAACA[G/T]GAAAAGGTCACTGAG | 226747 |
rs32653724 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Ahctf1 | Mm_Celera | 1:179751191 | CCCAACTCTCAAATA[G/T]CTCTTGTACCTCCAG | 226747 |
rs32653726 | snp | A/G | 0.495868 | 0.0452663 | synonymous-codon | Ahctf1 | GRCm38.p3 | 1:179752506 | CTGCTCCACCCGCCA[A/G]GTCTGAGACTGCCGC | 226747 |
rs32653730 | snp | A/G | 0.142012 | 0.225474 | synonymous-codon | Ahctf1 | Mm_Celera | 1:179752726 | ACCAGTTGTGCCACC[A/G]TCAGCTTCTAAGGGA | 226747 |
rs32653733 | snp | A/G | 0.375 | 0.216506 | synonymous-codon | Ahctf1 | GRCm38.p3 | 1:179753119 | AGAAGGAGTTTCTTC[A/G]GCTGCTGGCTCGGGT | 226747 |
rs32653794 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ahctf1 | Mm_Celera | 1:179763262 | GATGTCACCAAATAT[C/T]AAAATATATAGTTTC | 226747 |
rs32653797 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179763369 | TATATTGGCTTAGCT[C/T]AAATATAGGCTAAAG | 226747 |
rs32653800 | snp | A/T | 0.408163 | 0.193609 | synonymous-codon, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179763518 | CATGAATGAAATCCT[A/T]GTTTCTTTAACTCTG | 226747 |
rs32653803 | snp | A/G | 0.497778 | 0.0332592 | missense, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179763595 | AAGGTGTTGTTCGAA[A/G]ACCAGACCTAAGGAT | 226747 |
rs32653855 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179801717 | AGAATAGACATGCTA[C/T]GGAGACCTTTAAGCT | 226747 |
rs32653896 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179784103 | ACCTTCTATTATCCA[C/T]GTTCTGATGTAACCA | 226747 |
rs32653899 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179784316 | AAAGTTACAGCACTA[A/G]GGAGAGTAAGACAGG | 226747 |
rs32653901 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179784506 | TTCTTTAGCAGTACT[A/G]GAGCCTAGGACACAA | 226747 |
rs32653905 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Ahctf1 | Mm_Celera | 1:179749676 | CAAAGTAAGCCATAG[A/G]AAAGAAATGCGGCAT | 226747 |
rs32653908 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ahctf1 | Mm_Celera | 1:179749689 | AGAAAAGAAATGCGG[C/T]ATGCAGACTCTCCTT | 226747 |
rs32653911 | snp | G/T | 0.42 | 0.183303 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179749758 | GTGCAGAGATTACAC[G/T]CGGGACTCTGAACTC | 226747 |
rs32653913 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Ahctf1 | Mm_Celera | 1:179749938 | CAAATAGACAGATGA[C/T]CAATGTCAGACGTCT | 226747 |
rs32654250 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179765801 | ATATCCAGAGTTAGG[C/T]TGTAACTAGTAATAA | 226747 |
rs32654253 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179766309 | GTCATCTTCAAGTTA[C/T]AGTATCTGGTGGCCC | 226747 |
rs32654366 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Ahctf1 | Mm_Celera | 1:179758115 | TTGTTATAAAAACTA[A/G]AATTCAGAACCCACT | 226747 |
rs32654371 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Ahctf1 | Mm_Celera | 1:179758360 | TGTTTTTCAGGCAAG[C/T]CTGTCAAGTGTCCAG | 226747 |
rs32654715 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ahctf1 | Mm_Celera | 1:179750333 | TGATACAGATCTTAC[A/G]CTGGAATTTTACACA | 226747 |
rs32654804 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179773527 | GTATTCTACATAACT[A/G]CAACAAAACTAACAA | 226747 |
rs32654807 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179773550 | ACTAACAACATATCA[A/T]AAACTTAAACTCTCT | 226747 |
rs32654813 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179774137 | GAAGGTGGTACTGTT[C/T]ATAAAGTTAAAATCT | 226747 |
rs32654886 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179766734 | CTGCTGAAATTGCTT[A/G]GAAAAGTAACCAGCT | 226747 |
rs32654893 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179767295 | TAATATTCACTTTCT[C/T]ATTACACTGGAGACC | 226747 |
rs32654945 | snp | A/C | 0.277778 | 0.248452 | missense, downstream-variant-500B | Ahctf1 | GRCm38.p3 | 1:179753413 | ATTCAGGCTTAGGGC[A/C]TGCTGCCTTCTTGTG | 226747 |
rs32655047 | snp | A/G | 0.5 | 0 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179759428 | TCACTGCTGGAGAGT[A/G]TCTCCCTATAATAAC | 226747 |
rs32655049 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179759469 | CTGAAACTCACATTC[C/T]TCTCTCAGCCTCTGT | 226747 |
rs32655050 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179759510 | ACCTAAACTAGACCG[C/T]GTTTCAGACAGCAAG | 226747 |
rs32655052 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179759565 | TGCGGGTACTTCTTA[C/T]GCATATTTTTGAATG | 226747 |
rs32655226 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179785877 | TGCTAAAAACATTTA[G/T]ATGACTTCTAGCAAG | 226747 |
rs32655229 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179786149 | TAAAAAGAAAAAGAT[A/T]TTAAATTTTGAATTA | 226747 |
rs32655231 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179786545 | GACATTTTCTAAAAA[A/G]CTCAAAATTTATAAA | 226747 |
rs32655668 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179774507 | ATACTGAAACATTTT[C/T]AACTATCAGCTATTT | 226747 |
rs32655670 | snp | A/G | 0.32 | 0.24 | intron-variant | Ahctf1 | Mm_Celera | 1:179774808 | CTTACATAGCCAATG[A/G]TTGATGATGGTGGTG | 226747 |
rs32655742 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179768019 | GGCCCAGAAGAAATC[A/G]TCACCTAGTCAGCCA | 226747 |
rs32655864 | snp | C/T | 0.152778 | 0.230321 | synonymous-codon, downstream-variant-500B | Ahctf1 | GRCm38.p3 | 1:179753674 | CGGTTCAGGCACATA[C/T]GGTAAAGTCTCTACC | 226747 |
rs32655867 | snp | A/T | 0.493827 | 0.0552116 | missense, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179753766 | GGGGTTCCCTGTGGC[A/T]CACAGGTTTTTCCTT | 226747 |
rs32655869 | snp | C/T | 0.473373 | 0.11227 | synonymous-codon, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179753791 | TTCCTTGGTCGCTTT[C/T]GGTAACATATTAGGT | 226747 |
rs32655872 | snp | C/T | 0.132653 | 0.220748 | missense, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179753799 | TCGCTTTCGGTAACA[C/T]ATTAGGTGCTGCAGA | 226747 |
rs32655924 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179787426 | CCTACAATGGACGTC[C/T]GTGGTTTAATCCTTT | 226747 |
rs32655927 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179787817 | ACTTATCTATCCCTG[A/G]GATCTTTACTCTGAA | 226747 |
rs32655930 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179788089 | TGAATAAATGACATA[A/C]ACAGGACCTTAATTT | 226747 |
rs32655932 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ahctf1 | Mm_Celera | 1:179788401 | TCTAAAATGAAATAT[C/T]CCCATGCTAAAAGTT | 226747 |
rs32656254 | snp | C/G | 0.426035 | 0.177515 | missense, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179760283 | CAGACTGACGACACA[C/G]CAAAAGAAGCTTCAG | 226747 |
rs32656256 | snp | A/G | 0.489796 | 0.070696 | synonymous-codon, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179760351 | TGCTTCCACTGCAGC[A/G]TCTCCCGTGCCTGTA | 226747 |
rs32656259 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179760442 | GTTCTCGTTTTAATT[C/T]CTTGGCATCAGGCTG | 226747 |
rs32656262 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179760510 | GGCCCCTCTTAACTC[A/G]CACTTCTCCCTTTTG | 226747 |
rs32656495 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ahctf1 | Mm_Celera | 1:179774919 | TGTGCACACGTGGTA[C/T]GTACACATACTTACA | 226747 |
rs32656497 | snp | C/G | 0.32 | 0.24 | intron-variant | Ahctf1 | Mm_Celera | 1:179775073 | CCTAATCTGTCCATG[C/G]AAGAGACAAGCCATG | 226747 |
rs32656500 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179775445 | TCCCTGACTCATAAA[A/G]GCTTCAATTATCTTT | 226747 |
rs32656502 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179775784 | CACCAGAACCCAAAC[A/G]AATCTTTTAGCACAG | 226747 |
rs32656587 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Ahctf1 | Mm_Celera | 1:179754119 | AATGAATTATAAAGT[A/T]CATTTTGATCTAAAG | 226747 |
rs32656590 | snp | C/T | 0.42 | 0.183303 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179754185 | GTCCATTTTAAAATA[C/T]AAACTACACTTGACT | 226747 |
rs32656592 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ahctf1 | Mm_Celera | 1:179755153 | CAAGCAGTTAATACG[C/T]CTCAAGTAGTTAAAA | 226747 |
rs32656725 | snp | C/T | 0.124444 | 0.216185 | missense, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179789672 | AAATTTGCCCTGATG[C/T]CAAACATTTTCTATC | 226747 |
rs32656727 | snp | A/G | 0.32 | 0.24 | intron-variant | Ahctf1 | Mm_Celera | 1:179789813 | TTTACATAACACATA[A/G]AATGCATATGGCAAA | 226747 |
rs32656730 | snp | C/T | 0.32 | 0.24 | intron-variant | Ahctf1 | Mm_Celera | 1:179789870 | ATGTAACTAATGCAG[C/T]ATGTGGTATAGTCTA | 226747 |
rs32656764 | snp | C/T | 0.5 | 0 | intron-variant | Ahctf1 | Mm_Celera | 1:179768089 | TGACAGCTTGTTTTC[C/T]TCAGGGTTTTAATAT | 226747 |
rs32656767 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ahctf1 | Mm_Celera | 1:179768134 | CATTAAGCCACATGA[A/G]GTAAGTAAACAGAAA | 226747 |
rs32656769 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ahctf1 | Mm_Celera | 1:179768415 | GGACTACAAAGAAAA[A/G]ATACTCAGTTTTAAA | 226747 |
rs32656771 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179768442 | TAAATTGTGTGTCAC[A/T]TGGCTTATTGGCAAA | 226747 |
rs32656773 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179768536 | TGCACTGTTGCCAAA[C/T]AGCAATAAACAGTCA | 226747 |
rs32657293 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179761803 | AGTAGGCAATTGGTT[C/T]ATCGATTCTAAACCA | 226747 |
rs32657445 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179755154 | AAGCAGTTAATACGT[C/T]TCAAGTAGTTAAAAA | 226747 |
rs32657452 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179756016 | CTAGCCACCTTCATT[A/T]GCAGAACTCTACAAG | 226747 |
rs32657715 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179768567 | TTTGAAAATCTTACA[C/T]GGGGCCAAAAAGAAG | 226747 |
rs32657717 | snp | C/G/T | 0.459184 | 0.136902 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179768602 | AGCAGGTAGACTTCC[C/G/T]TGGGAGAGAACTGCC | 226747 |
rs32657719 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179768616 | CTTGGGAGAGAACTG[C/T]CTGGGAAAGCCTCTG | 226747 |
rs32657722 | snp | C/T | 0.48 | 0.0979796 | synonymous-codon, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179769018 | GACGCCATTTCTAGG[C/T]TCATGACTTGCCCAC | 226747 |
rs32657805 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179775976 | CTAGTATAATAATCT[A/T]CAAAAGCGTATATTC | 226747 |
rs32657808 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179776014 | GTTACTTACCTCATA[A/G]TCATTATGATCTAGC | 226747 |
rs32657813 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179776712 | TAACTTTAAAAACTC[A/G]TTTGTCGTGTGTGGG | 226747 |
rs32657858 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179790947 | CTTGAGTTTAAAGTC[A/C/G]ATTTTCTACAACAGA | 226747 |
rs32657861 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179791249 | TGCACATGTAACAAT[C/T]GCCCGGATGCTGTAT | 226747 |
rs32658510 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Ahctf1 | Mm_Celera | 1:179756352 | AGATGATTTTCACCC[A/G]TGTTTGCCACCATAA | 226747 |
rs32658516 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179776796 | AGACATCAGAAGTTA[C/G]ATACTGTGCTAATAA | 226747 |
rs32658518 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179776823 | ATAACTCACCAAATA[C/G]TGCTCACTCTCTGAT | 226747 |
rs32658521 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179777131 | TGAGAATGGCAGCTC[A/G]CTCCCAGCAGTATTC | 226747 |
rs32658563 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179762193 | AAGTCTAAAATTCCA[A/G]TAGTCCCTCAGTTTA | 226747 |
rs32658614 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179793274 | TACAGATCCATCCAC[A/G]TTCCCCTGAGCTCAC | 226747 |
rs32658617 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179793847 | CAGAATGGGATTAGA[A/G]GCTAAATCAACTGTA | 226747 |
rs32658619 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179794235 | TCAACAAACAGAATA[A/T]TTATTTTACGATAGC | 226747 |
rs32658622 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179794395 | TCAAAGCAATGCTGT[C/T]TTCAGTTTAGAGCTT | 226747 |
rs32658754 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Ahctf1 | Mm_Celera | 1:179769487 | TAATAAAGTTTTAAT[G/T]TTCCTAATTTTAGGT | 226747 |
rs32658756 | snp | A/G | 0.18 | 0.24 | intron-variant | Ahctf1 | Mm_Celera | 1:179769608 | CCTCCTTAATTGTAT[A/G]CACATTTATACATCC | 226747 |
rs32658759 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179769657 | CTCTGATACTTCACA[A/G]CTCATACAATGTAAC | 226747 |
rs32658761 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179769737 | CTGACATGGCCATGG[A/C]CGTGTCAAGACAAAA | 226747 |
rs32659245 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179794443 | CATCACCCAATGTAA[C/G]AAGAGTAAACTAATC | 226747 |
rs32659247 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ahctf1 | Mm_Celera | 1:179794481 | AAAAAAGTTTAGTTT[A/G]CCTTTCTGCAGTGCT | 226747 |
rs32659250 | snp | A/G | 0.277778 | 0.248452 | synonymous-codon, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179795874 | ACCGCTCTCCTGTTA[A/G]GGAGTTTACAACTTC | 226747 |
rs32660116 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ahctf1 | Mm_Celera | 1:179796684 | AAACTCAAACCAAAC[A/T]GATCCTACATTTTCT | 226747 |
rs32660120 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Ahctf1 | Mm_Celera | 1:179797452 | AAAGGTAGATGAAAG[A/C]TATATCTGTAGTCAG | 226747 |
rs32660123 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ahctf1 | Mm_Celera | 1:179798338 | AATATATTTTGAGAA[C/T]TTAAAACCTCTTACA | 226747 |
rs32660986 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Ahctf1 | Mm_Celera | 1:179798494 | CCTGCTGCAGGTTAC[C/T]GTAAACACTTTACTG | 226747 |
rs32660989 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179799655 | GACAAACAGGTAAAC[A/G]TGGGGAATGTCCACA | 226747 |
rs32660991 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179799786 | TTCTGTAAAAATGAA[A/G]AAAACTCCATAATGT | 226747 |
rs32661102 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179771923 | TTTAATCCCAGCACT[C/T]GGGAGGCAGAGGCAG | 226747 |
rs32661774 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179800486 | GCTCAGCCCTAAAAC[A/G]GAGCTTAATGCACTC | 226747 |
rs32661777 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahctf1 | Mm_Celera | 1:179800572 | CTCAACGTCCACTTG[A/G]AAGGCAGTAAGACTA | 226747 |
rs32670704 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179780516 | TGATTAATATTATCT[C/T]GATCTGTCTACGTGA | 226747 |
rs32685133 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179747351 | GTCTCTCTGTAGCCC[C/T]GGAACTCATTTTGTA | 226747 |
rs32690623 | snp | A/G | 0.32 | 0.24 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179791348 | GACATGAGTACACTC[A/G]GAGGGGTACCCAAGA | 226747 |
rs32707605 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179761474 | CCACAACCACCCATA[A/G]TGATATCTGATGTCC | 226747 |
rs32752268 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179798141 | GAGCACTCACTGTTC[G/T]TGTGATGACCTGGGT | 226747 |
rs32800056 | snp | G/T | 0.32 | 0.24 | intron-variant | Ahctf1 | Mm_Celera | 1:179771736 | CAGAGACTCATGGAC[G/T]AACATGTGCTCACCA | 226747 |
rs32816257 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ahctf1 | GRCm38.p3 | 1:179762475 | CATTTTACTATGGTA[A/G]GAAATATTCTATTAC | 226747 |
rs45897844 | snp | C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179763791 | CTTTGATCCCAGCAC[C/T]TGGGAGGCAGAGACA | 226747 |
rs45899424 | snp | C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179763769 | GCCGGGCAGTGGTGG[C/T]GCACACCTTTGATCC | 226747 |
rs46066043 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179763226 | CTCCACAGTCTTTCA[A/T]TAAAAACCAAACCAT | 226747 |
rs46209136 | snp | C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179760181 | GATTAAGGTGTGTAT[C/T]ACCATTCCTAGCCTC | 226747 |
rs46782354 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179772080 | GCTCCAGCCACCACA[C/T]CCCCAGCTGTGACGA | 226747 |
rs46983460 | snp | G/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179772918 | TCACTGTGGGTGCAG[G/T]CTTGAAGACCCTCAT | 226747 |
rs47028136 | snp | G/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179764442 | AATAAACCTTTAATT[G/T]TCTCTGATTGCAGTC | 226747 |
rs47284023 | snp | A/G | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179758727 | ATCTCTGAATCTGAG[A/G]ACAGCCTGGCCTTCA | 226747 |
rs47288247 | snp | A/C | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179776847 | CTCTGATTTCCCCCG[A/C]CCCCAGCCCCGGAAA | 226747 |
rs47515452 | snp | C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179758686 | AGCTTGTCCAGGTGC[C/T]GACAGAGGGAGGCAG | 226747 |
rs47737788 | snp | C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179781569 | CTCTTTATACAATGT[C/T]TTACCAAGTAAACAA | 226747 |
rs47778531 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179763804 | ACTTGGGAGGCAGAG[A/G]CAGGCGGATTTCTGA | 226747 |
rs47915876 | snp | A/G | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179763770 | CCGGGCAGTGGTGGT[A/G]CACACCTTTGATCCC | 226747 |
rs47942988 | snp | G/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179760187 | GGTGTGTATTACCAT[G/T]CCTAGCCTCAGCAGT | 226747 |
rs48226939 | snp | C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179764443 | ATAAACCTTTAATTT[C/T]CTCTGATTGCAGTCA | 226747 |
rs48363090 | snp | G/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179750416 | TTTTTTACATGGATC[G/T]TGGGGATTCAATCTC | 226747 |
rs48515903 | snp | A/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179784315 | TAAAGTTACAGCACT[A/T]AGGAGAGTAAGACAG | 226747 |
rs48536263 | snp | A/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179760242 | GTGTCTCCAACCTTC[A/T]CCTCTGCTCCAGAGC | 226747 |
rs48641814 | snp | C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179769676 | ATACAATGTAACACA[C/T]ACTCTGCTCCTTCAA | 226747 |
rs48919518 | snp | A/C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179766365 | TTTTATTTAAGAGTG[A/C/T]GTGCGTGCGTGCGTG | 226747 |
rs49000273 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179761408 | GGGCTGGTGAGATGG[C/T]TTGGTGGATAAGAGC | 226747 |
rs49016854 | snp | C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179769277 | AGTACCCTCCCTAGC[C/T]CGAGTACAAGCATTC | 226747 |
rs49255085 | snp | C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179795218 | GTAGCCCTAACTTAT[C/T]GGTAACTATACATAG | 226747 |
rs49819092 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764360 | TTAAAGTCAGCCTAG[C/T]CCACAAAGTAAGTTC | 226747 |
rs49970517 | snp | A/C | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179760243 | TGTCTCCAACCTTCT[A/C]CTCTGCTCCAGAGCT | 226747 |
rs50051803 | snp | C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179750424 | ATGGATCTTGGGGAT[C/T]CAATCTCAGGTCATC | 226747 |
rs50056629 | snp | G/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179768914 | TCTCTGCCCTCCACA[G/T]GCACCCTGACACCCA | 226747 |
rs50624045 | snp | C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179785765 | GTGAGACCCCGCCCC[C/T]TCCCATCTCTAAAAT | 226747 |
rs50978320 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179769494 | GTTTTAATGTTCCTA[A/T]TTTTAGGTGTTGCTA | 226747 |
rs51142999 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179789591 | TTGAACATAAGAGTA[A/C]CAGTACAATAAAAAA | 226747 |
rs51152221 | snp | C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179769680 | AATGTAACACATACT[C/T]TGCTCCTTCAAAGCT | 226747 |
rs51252456 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179797085 | CTGGACTCGGATGTA[A/C]CTGTTACTGTGGTCT | 226747 |
rs51527655 | snp | A/G | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179758703 | ACAGAGGGAGGCAGA[A/G]GCAGGCAGATCTCTG | 226747 |
rs51594511 | snp | C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179768084 | AAGTCTGACAGCTTG[C/T]TTTCCTCAGGGTTTT | 226747 |
rs51825941 | snp | C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179764970 | GAACCGACTGCTCTT[C/T]GGGAGGTCCTGAGTT | 226747 |
rs51938968 | snp | A/G | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179770193 | GGTCCACCCCTGGAT[A/G]TGGATATGGTGGATA | 226747 |
rs52236471 | snp | A/C | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179764256 | TCATAAAAATAAATA[A/C]ATCTTTAAAAAAAGA | 226747 |
rs52333396 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179763909 | CAAAACAAAACAAAA[A/C]AAAAAACAAAAAACA | 226747 |
rs52621710 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805930 | GGTGACCTTTTGGGC[A/G]TTTGTTCGTTAATCA | 226747 |
rs52625393 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179763868 | CAGGACAGCCAGGGC[A/T]ATACAGAGAAACCCT | 226747 |
rs52645571 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805938 | TTTGGGCGTTTGTTC[A/G]TTAATCATCTGCAGA | 226747 |
rs52646979 | snp | A/C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179763870 | GGACAGCCAGGGCAA[A/C/T]ACAGAGAAACCCTGC | 226747 |
rs107726667 | snp | A/G | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179768666 | AAATACAAGATGTTT[A/G]AAATGTGAACTTAAT | 226747 |
rs108541490 | snp | A/G | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179768659 | CACCCACAAATACAA[A/G]ATGTTTGAAATGTGA | 226747 |
rs211717209 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179777028 | TCAGGTCCTCGTGCT[C/T]CTATAACAAGCACTT | 226747 |
rs211780402 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179766943 | TGCTGGTATTAAAGG[A/C]GTGCACCACCACACC | 226747 |
rs211888200 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179757667 | CCAACATGCTCATGG[C/T]CAGCTTCTACTTCTC | 226747 |
rs211893160 | in-del | -/TG | | | intron-variant | Ahctf1 | Mm_Celera | 1:179784220 | AAAAGAAAGACACTC[-/TG]AAATCAGAGGCAGTA | 226747 |
rs211919169 | in-del | -/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179788649 | AATTCTTAAGAATAG[-/T]TTTTTTTTTGTTTTA | 226747 |
rs211920321 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179747696 | AGGCCAGGTTCTCTC[C/T]ATCTTATAGGCATTG | 226747 |
rs211920464 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179758655 | CAACTAAATCTTCAC[A/C]ACTTGCCCAATAACC | 226747 |
rs211962872 | snp | C/T | | | synonymous-codon | Ahctf1 | Mm_Celera | 1:179748671 | TTCTTTCAGCTGGGC[C/T]GCGGCCTCCATGTTC | 226747 |
rs212048091 | in-del | -/TCC | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179790863 | ACCTGACCCTCCTAA[-/TCC]TCCTCCTCCTCCTCC | 226747 |
rs212136303 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179755092 | CAGATATGCAGGGAG[A/C]TCCTGTTTACTATAT | 226747 |
rs212179748 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179745461 | TGCTCACACTCTTCC[A/G]TTCTCTGTAACCTGT | 226747 |
rs212216990 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179745979 | TCGCCCTCATTTTAA[A/G]ACAGTTCTAGTATCT | 226747 |
rs212249334 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179802640 | TTTAGGAACCGAAAA[A/T]TCACAAGATCCCATG | 226747 |
rs212276951 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179799431 | AATCTGAGGGAGAGC[A/G]AGCCCCATTCAAAAG | 226747 |
rs212313351 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179800322 | AGTTCCAAAGAGGCA[G/T]ACTCTTCAGGCTAGA | 226747 |
rs212383201 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792774 | AATGTACACCATGAC[-/A]ATACATGTCCTCTTA | 226747 |
rs212452595 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179787621 | GACAGAGAATAAGAA[A/G]AGGGATGGCATGTTA | 226747 |
rs212488520 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179789213 | AGATGGTTGTGAGCC[A/G]CCATGTGGTTGCTGG | 226747 |
rs212580722 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179751200 | CAAATATCTCTTGTA[A/C]CTCCAGCTACCTAAT | 226747 |
rs212620688 | in-del | -/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179752155 | TTTATCTGGTGGTTT[-/G]GGTTTTTTGGGAGTA | 226747 |
rs212636068 | snp | C/T | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805803 | TTCCTCTTCTGTCTA[C/T]ATTCCCATCCTTTGG | 226747 |
rs212724836 | in-del | -/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179776423 | AAATTCAAGTAACTT[-/G]TTTAGTAAATTTTTA | 226747 |
rs212772298 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179781402 | AAAAGCCAGGAGACC[A/T]AATTCAATCCCTAGG | 226747 |
rs212859774 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179804017 | CCGTCTATGACTGCT[A/G]CTCTTGCCTCCGTTT | 226747 |
rs212902916 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179790982 | GGTCTATGAGACGGC[G/T]CAGCCTGTGAATCAT | 226747 |
rs212907882 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179783096 | ACTAACTTCGAAATG[A/G]AAGTTACTAACTTTG | 226747 |
rs212978635 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805410 | CTGCAAGATGTAAAA[A/G]TGTGCTAGTTTGCGC | 226747 |
rs213015248 | in-del | -/TAAAT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179796038 | TAACTCAAAAATAAA[-/TAAAT]TAAATTAAAATAAAA | 226747 |
rs213018278 | in-del | -/AG | | | intron-variant | Ahctf1 | Mm_Celera | 1:179780724 | TAATCCAATGAATAT[-/AG]TGTCTGTGAGGCAAT | 226747 |
rs213046066 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792043 | AGCAAATGGGTCATC[A/G]AATTGACTGTAATGC | 226747 |
rs213083412 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179779118 | TGTGAAAGGCACTGT[C/T]TCCTCAGTTTCTGTC | 226747 |
rs213101477 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179787903 | AAAACAAAATAACAG[-/A]AAAAAAAAAAACCCA | 226747 |
rs213117407 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179769734 | GTGCTGACATGGCCA[C/T]GGCCGTGTCAAGACA | 226747 |
rs213119840 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179780115 | CATTTACTTAAGTGA[A/G]AATGTAAGGGAAGTG | 226747 |
rs213304358 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750184 | ACCACCAAAAAACCA[A/G]CAAAAACAAACTCCA | 226747 |
rs213349081 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179785784 | CATCTCTAAAATAAG[C/G]ACCCAGAAGATGCAA | 226747 |
rs213476754 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179774701 | ATTATGTGCTTACTA[C/T]AGGACTTGCCTTGAA | 226747 |
rs213562150 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179768905 | CTAAATAGTTCTCTG[A/C]CCTCCACAGGCACCC | 226747 |
rs213598188 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764368 | AGCCTAGCCCACAAA[G/T]TAAGTTCCAGGGTAG | 226747 |
rs213601280 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179759994 | ATGTAGGTTCTTAGA[A/G]TTGAATTTGGATCCT | 226747 |
rs213638248 | snp | A/G/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179755389 | ATTAAGTTTAAATGA[A/G/T]CAACTTTAAAGCCCA | 226747 |
rs213786938 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179799097 | TGCCCCTGCATCTAT[A/G]TATGACTATGCATAT | 226747 |
rs213875834 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179762139 | TGAGGGCAGAGAGTA[C/G]AATCAAAGTCCTGGT | 226747 |
rs214002547 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764263 | AATAAATAAATCTTT[-/A]AAAAAAGAAAAGGAA | 226747 |
rs214067251 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764898 | ATCCTATCCAAAAAA[A/C]CCAAACCAATCAAAA | 226747 |
rs214080020 | snp | A/G | | | missense | Ahctf1 | Mm_Celera | 1:179752946 | TTCTGAGTATCTTCT[A/G]AATTGGCATTCCTCA | 226747 |
rs214114218 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179756536 | TAAAAGTATTAAATA[A/C]GTTTTTTTAAATTAA | 226747 |
rs214245271 | in-del | -/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179801343 | AGGTATTCATAATCG[-/C]AATATAAGATGCAGG | 226747 |
rs214299382 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179798226 | ATGCCCTTTTCTGAC[C/T]TCTGAGGGCACTGTA | 226747 |
rs214313939 | in-del | -/TA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793439 | TAGGTACACATAATT[-/TA]AAAAAAAAAAATTCT | 226747 |
rs214377799 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179804295 | GAGAGACGAGGAGTT[A/G]GGCAGACCCTTAGTA | 226747 |
rs214412592 | snp | C/T | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805109 | AATGTGTCTTTATTA[C/T]TGAGTTGTAAGAGCA | 226747 |
rs214450112 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179759780 | TGACACTGGAGTTTA[C/T]AGACAGCTGTGAAGC | 226747 |
rs214459877 | snp | G/T | | | missense, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179762802 | CTTCCTGAATGGGTA[G/T]CCAGTGACTCTGCCA | 226747 |
rs214470270 | snp | A/T | | | intron-variant, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179746566 | TAGGAATGGGCACAA[A/T]GTGCTGTCTGGTCAA | 226747 |
rs214474066 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179772204 | CTTGATCCCACTGAC[-/A]AGACTTGTTTTAGAG | 226747 |
rs214504193 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179747356 | TCTGTAGCCCTGGAA[C/T]TCATTTTGTAGACCA | 226747 |
rs214507475 | snp | A/G | | | missense, downstream-variant-500B | Ahctf1 | Mm_Celera | 1:179753504 | TCCTTAACAGTCTTC[A/G]GTGTAGAGTTTGTCA | 226747 |
rs214683553 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179777102 | TGCTATTTATTTTCA[G/T]CACTTAACTCCATTG | 226747 |
rs214818203 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179767124 | ATAAACAAAACAAAC[A/T]GAAGCGATCATGTAA | 226747 |
rs214821951 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805836 | CAAATTTCCTTCCAT[A/G]TCAGACTCCTTGGTA | 226747 |
rs214825051 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179748761 | AAAACAAAAGGCAAT[C/T]AATATACAGCAGCAA | 226747 |
rs215069962 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179772187 | AATTAATACAGTGTT[C/T]AACTTGATCCCACTG | 226747 |
rs215081678 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179790849 | TATGTAGTGAAGCTG[A/T]CCTGACCCTCCTAAT | 226747 |
rs215159625 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792203 | CCTAAACTCACATGC[G/T]AGGTAATTTCCTTAC | 226747 |
rs215199527 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179762202 | ATTCCAGTAGTCCCT[A/C]AGTTTATAAACTTGG | 226747 |
rs215230828 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179779235 | ACAGAAGTTTCTTGT[C/T]GGAATTTGTAGGGTC | 226747 |
rs215389742 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179770202 | CTGGATGTGGATATG[C/G]TGGATATGGCAACCA | 226747 |
rs215409333 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179801452 | AAGTGCACAGCCACC[C/T]GTTGGCAGAGGCAGG | 226747 |
rs215454604 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179795992 | GTAAATCCCTCCTGA[A/G]TTAAAAGCAAAGCAT | 226747 |
rs215751624 | in-del | -/GTAA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179797038 | CTCACCCTACTCCTG[-/GTAA]GTAATTCCAATAAAC | 226747 |
rs215765981 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179756758 | AGTCACCTACTATCT[C/T]CTCTTCCCAAAGCAC | 226747 |
rs215766018 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179766407 | ACGCGCGCTCTCGGA[A/G]GATGACCCGATCCTG | 226747 |
rs215789392 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793099 | CAGCAACCACATGGT[A/G]GCTCACAACCACCTA | 226747 |
rs215832932 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179780280 | TCAGTATTTACATTA[C/T]TAGACTAACAGAAAC | 226747 |
rs215860203 | in-del | -/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179760250 | ACCTTCTCCTCTGCT[-/C]CCAGAGCTTACCCTT | 226747 |
rs215888978 | in-del | -/CC | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805202 | GGCTACATAGAGAAA[-/CC]CTATCTCAAACAAAC | 226747 |
rs215902063 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179789125 | TTTTTTTTTTTTTTT[-/A]AAGATTTATTTTATT | 226747 |
rs216032377 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179783805 | TAAAGAATGAATAAA[C/T]ATTCACACTGGGGTG | 226747 |
rs216119400 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179751430 | GTGTAGGCATGAGGA[A/G]GTCCCTGCAGTAATG | 226747 |
rs216221931 | in-del | -/ACAGAGA | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179764457 | TCTCTGATTGCAGTC[-/ACAGAGA]ATATAAAAATGTGAT | 226747 |
rs216263609 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179799376 | AAATAATGATGATTG[C/T]TCTATTACACAGTAC | 226747 |
rs216306777 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179800130 | AATTCTGGTTAAATA[A/G]AAAAGCATCTATCTG | 226747 |
rs216353457 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179759803 | TGTGAAGCATCTCAT[A/G]TATATGGATGGTAGG | 226747 |
rs216373261 | in-del | -/ATTT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179755324 | TATATGCCACAAAAC[-/ATTT]ATACTTATTTTTTGA | 226747 |
rs216419634 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750553 | CTCCCCACCAGCTGA[G/T]GAGAGGCAGACCTTA | 226747 |
rs216436099 | in-del | -/AAAC | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764912 | AACCAAACCAATCAA[-/AAAC]AAACAAACAGGGGCT | 226747 |
rs216479983 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179804541 | CTAAAGTAGGTCAGG[A/G]AGGTTTTAGAGGTTT | 226747 |
rs216509974 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805252 | ACAAACAAACAGAAG[A/G]GGGAAGAGAGAAGGA | 226747 |
rs216529429 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750707 | TCCAGTTAAGCTTCC[A/T]CATGTACTTTTAAGA | 226747 |
rs216549743 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179746663 | GTCCCCATGTGTGCC[A/G]GGGGGCATACTCAGC | 226747 |
rs216560564 | in-del | -/TAAAATTTACTCTTG | | | intron-variant | Ahctf1 | Mm_Celera | 1:179758154 | ACATTTTAAATTTTA[-/TAAAATTTACTCTTG]TAAAATTTATAAAAT | 226747 |
rs216642963 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793189 | CATTAAAGTTTAAAA[A/T]AATTTTTGCTAAAAG | 226747 |
rs216676522 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793967 | TCTAAGAAAACAGTG[A/C]AACTCTCAAATATAC | 226747 |
rs216709360 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179801594 | TAAGCTGACATGCCT[C/T]AAAAGATGAGCACCC | 226747 |
rs216746928 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179787525 | ACCACGGCAGTGGAA[C/T]GGCACCAGAAGGGGC | 226747 |
rs216793150 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179775945 | CTATGTCAAAATTAA[A/C]GTAGTTATACACGTT | 226747 |
rs216799212 | snp | C/G | | | missense, downstream-variant-500B | Ahctf1 | Mm_Celera | 1:179753648 | AGATTTTCTGCAATT[C/G]CCACTTTAACCGGTT | 226747 |
rs216830894 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179802480 | AAAAAGCACCCAAAC[C/T]CAGCGACTTGGTTAG | 226747 |
rs216917515 | in-del | -/AACAACAAA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179752248 | AACAACAACAACAAC[-/AACAACAAA]AAAACCCTCAAAATT | 226747 |
rs216929347 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179768159 | CAGAAATAAGTGTAA[C/T]TTGATTTATAGTTTC | 226747 |
rs217051997 | snp | A/G | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179758745 | AGCCTGGCCTTCAGA[A/G]TGAGATCCAGGTCAG | 226747 |
rs217081165 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179747432 | TCCAGGATTAGAGGC[A/G]CGCACCACTACCACC | 226747 |
rs217128252 | in-del | -/AGAAT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179772628 | AGTGGTTACTATATA[-/AGAAT]AGAAGGCTGGCCTGG | 226747 |
rs217195609 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179797997 | AAAGCATGCTAACTA[A/G]ACATTTTAGATGTGT | 226747 |
rs217195663 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179783410 | AAAGACCCCAAATCA[A/T]GGTAGGCATAATGGC | 226747 |
rs217231348 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179784065 | CCACCCAAAATATTC[C/T]ATTTTTACAAAGTGA | 226747 |
rs217327645 | snp | C/T | | | intron-variant, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179754496 | ATTCACCTACATAAG[C/T]TCCCTTGGGCTAGAC | 226747 |
rs217359907 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179786188 | CTGTAGGTAATTAAA[A/T]TTTTATATTGAATAA | 226747 |
rs217448583 | in-del | -/CT | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805314 | AGCCTGTCTCTACTA[-/CT]CTCTCTCTCTGCACA | 226747 |
rs217474275 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179745302 | TCAATTATTAAGCGT[C/T]CATTCATTACACACT | 226747 |
rs217643317 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179761370 | ACCTTACATAAACTC[A/G]CTCAATAAAATTTTA | 226747 |
rs217708398 | snp | A/G | | | synonymous-codon | Ahctf1 | Mm_Celera | 1:179752780 | TTTCCTAGGGGTGGC[A/G]GGTACATCGAGTCCT | 226747 |
rs217739722 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179749904 | GCACATCACTGACAC[A/G]CAAAGAGAGACAGAC | 226747 |
rs217872896 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179745844 | TCACATGCCCACAAT[C/T]CAAATTCAACACAGT | 226747 |
rs217956654 | in-del | -/TA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179758615 | CTAGATAACAGTATC[-/TA]TAGTACTGATGACTA | 226747 |
rs217991858 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179797473 | CTGTAGTCAGGTGTG[A/G]TGACATACACCTTTA | 226747 |
rs218095474 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179798627 | GACCAGGCTGACCTC[C/G]AACTCAGAAATCCAC | 226747 |
rs218129633 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179784729 | TGTTTTACTGGCATG[G/T]ATGTATAAGATAAAT | 226747 |
rs218163199 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179790233 | ACAAACTGTTGCAGT[G/T]TGACTCCTTTGCTGC | 226747 |
rs218163697 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179786324 | TATGTACCAAGCACA[C/T]TGGACAAGAATAATT | 226747 |
rs218241140 | in-del | -/AC | | | intron-variant | Ahctf1 | Mm_Celera | 1:179761311 | ACCCCCAGTCAGATG[-/AC]AGATTTTTATTGTAT | 226747 |
rs218342005 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179791373 | CCAAGAGAGCATGCC[A/G]GTACACCCGGAGGGG | 226747 |
rs218401202 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179777953 | TTCATTTAGTATCAC[A/G]GGACTGTAGCGCTCA | 226747 |
rs218423397 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179778982 | CCTACCAATCAGTGA[A/G]CATGGGAGACCTTTC | 226747 |
rs218461727 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792705 | GAATCCAATTCCTGG[A/G]ACCCACATGATACAA | 226747 |
rs218491237 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179779539 | AAGTATAGGCATCAG[C/G]TTAATGTCAGTTATG | 226747 |
rs218504053 | in-del | -/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179791414 | GAGCATGCCAGTACA[-/C]CCGGAGGGGTTACCC | 226747 |
rs218522030 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179780689 | CATGTTTTCCCCCAA[C/T]TTGCTCTCATTTTAC | 226747 |
rs218554729 | in-del | -/TTAAA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179784193 | TCCTAAACCATGTTT[-/TTAAA]AAAAAAAAAAAAAAA | 226747 |
rs218662664 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179768830 | CTTTAAAAAAACAAA[A/C]ACTTGTTGCCTCCGT | 226747 |
rs218918165 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179749432 | AAAAAAAAAAGAAGT[A/G]CAAGAAATGGAGGGA | 226747 |
rs218955041 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179774416 | AAGCAGTATCATTAA[A/G]TAGTTAAAAAGCCAC | 226747 |
rs218962708 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179773444 | CCGATGTCTTGGACA[A/G]TACTGACAGTTTACC | 226747 |
rs219014215 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179763485 | TCTATCAGTCCAGTG[C/T]GTATTCATGCCTTCT | 226747 |
rs219113527 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764206 | CAGCCACATGATGAC[A/G]CACAACCATCAGTAC | 226747 |
rs219149265 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179770325 | TTTCTGAAGGTCTGC[C/T]CTTTGGGCTGTACAA | 226747 |
rs219243607 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179781122 | TTAAGATAACTGAGA[A/G]AAATAGGCATTTTAT | 226747 |
rs219258160 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179772514 | GATACAAGAGTCCTT[C/T]ACCTGAACCTTAGCC | 226747 |
rs219292377 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179773679 | AAGAAGTTAGAAGTC[A/G]TTCAACTTGAGCTAC | 226747 |
rs219310796 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179771172 | TTGCTGTTCTGGAAT[C/T]CACTCTAGCTGTTAC | 226747 |
rs219323148 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179745614 | CAGGCACACGTCGGT[A/G]CACTGTTTTATTTCT | 226747 |
rs219613808 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750929 | AAAATGTTTGGCCTA[C/G]TCGTGGTTTCTTTAA | 226747 |
rs219646816 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179751639 | AAAATGATCATTAAG[G/T]AAGTACGTTCATAGA | 226747 |
rs219874782 | in-del | -/AAAAAAAA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179802459 | CTCCAACTGTCTATT[-/AAAAAAAA]AAAAAAAAAAGCACC | 226747 |
rs219886202 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179781994 | CAGAACTACTACATG[C/T]CAAAAGATGTATATT | 226747 |
rs219891381 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179800976 | ACTTAAAAAAAATAC[C/T]ATAAACCAGTTTATG | 226747 |
rs219914103 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179783513 | CAGAGAGAGTGCCAG[A/G]ACAGCCAGGGCTACA | 226747 |
rs219939865 | in-del | -/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179774475 | TCAGAGAAGAGGTTA[-/T]TTTTTGTATGTTTGA | 226747 |
rs220245724 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764748 | CCTGAGACTTAGTCC[A/G]TATTACTACACAAGA | 226747 |
rs220250558 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179776200 | CAAAAGAAAAACCAT[A/G]TATATAGTTAGAGTA | 226747 |
rs220256295 | in-del | -/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179789454 | CAGCTTCTCTGCTAT[-/G]GGGGAAGAATATACC | 226747 |
rs220259250 | in-del | -/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179773769 | AATAGCTGCACATAA[-/G]GGCTTTTCATTTCTC | 226747 |
rs220260314 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179777438 | ATGAGATTAGGGTTA[G/T]ATATTTGAGTCTTAT | 226747 |
rs220281827 | in-del | -/CAAACAAACAAACAAA | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805209 | AGAGAAACCCTATCT[-/CAAACAAACAAACAAA]CAAACAAACAAACAA | 226747 |
rs220289991 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179778071 | CAGCAAAACGGCTGA[C/T]TGCTCTATTTTCCAC | 226747 |
rs220375792 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179801706 | AAGGCTGGATTAGAA[A/T]AGACATGCTACGGAG | 226747 |
rs220502790 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764698 | CAATAAATAATGTGG[-/A]AAAAAAACCAAAAAC | 226747 |
rs220544677 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179774949 | AACATATAAAGCACA[A/C]ATACACAAATATACA | 226747 |
rs220585949 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179770489 | CAGGACAATGTAAAC[A/T]AAGATGGTTATGAGA | 226747 |
rs220609938 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179760890 | CCTAAGAGAAACCCT[G/T]TCTTGGAAAACAAAA | 226747 |
rs220644511 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179761546 | TAATAGTAAATCTTT[A/G]GGCCGGAGCGAGCAG | 226747 |
rs220725746 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179774154 | TAAAGTTAAAATCTA[C/T]CCTCGTCCAAAGATT | 226747 |
rs220906036 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179763828 | TTTCTGAGTTCAAGG[C/T]CAGCCTGGTCTACAG | 226747 |
rs220919903 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179760229 | CAACAAGCTGTGTGT[A/G]TCTCCAACCTTCTCC | 226747 |
rs221000293 | snp | C/T | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179804547 | TAGGTCAGGGAGGTT[C/T]TAGAGGTTTTACAAC | 226747 |
rs221055130 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179768546 | CCAAACAGCAATAAA[C/T]AGTCATTTGAAAATC | 226747 |
rs221347113 | snp | C/T | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179804749 | TTTTTTTTTTTTTTT[C/T]CTTTCAGTTTGTTCT | 226747 |
rs221396715 | snp | A/C | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805477 | ACAAGATTTTGCAGT[A/C]AGTGTTGTGTGGTCT | 226747 |
rs221497618 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764527 | TTGTAAGTCAGGAAT[A/C]GGGGACAGTATAAGT | 226747 |
rs221580055 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Ahctf1 | GRCm38.p3 | 1:179803542 | CTTCGAACTCGTCCC[A/G]CCGCCCGCGCCGCGT | 226747 |
rs221588373 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179798419 | GTAAGGCCTTTCAAA[C/T]TTACCTCCTCCTAGC | 226747 |
rs221779063 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179801856 | CGGATCTCTCAGTTC[G/T]AGGACAGCCTGAGTT | 226747 |
rs221780320 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179799762 | TCTTCAACCCTATAA[A/T]GTTAATTTTTCTGTA | 226747 |
rs221804094 | snp | A/C | | | intron-variant, upstream-variant-2KB | Ahctf1 | GRCm38.p3 | 1:179803325 | CCGCCCCGCCCTCGG[A/C]GCGCGGGCCTGCGGT | 226747 |
rs221835709 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179800788 | CAAACTGATCTCAAA[A/C]TCTCAAGACATACCC | 226747 |
rs221847386 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792615 | AATTCAATTCCTACA[C/T]TCCACATAAAGGTGT | 226747 |
rs222130812 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179766146 | CTAATTTTAGGTAAG[A/T]ATATTAATGTACAAA | 226747 |
rs222132723 | in-del | -/AAA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179799835 | TCTTTTATTGGACAG[-/AAA]AAAAAAATCTAAATT | 226747 |
rs222164623 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179767229 | ACTGGGGAATGCATT[C/T]ATCTTCTGAGAAGGC | 226747 |
rs222165368 | in-del | -/GAA | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805451 | TCTAAATTGTGAGAG[-/GAA]GAAGTTAGACAAGAT | 226747 |
rs222181685 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179761471 | ATCCCACAACCACCC[A/G]TAATGATATCTGATG | 226747 |
rs222197566 | snp | A/C | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179757789 | AAAAAACCAAAAAAA[A/C]CCCAAAAGAGTTAGT | 226747 |
rs222223911 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179772759 | AAATGTTAAACTCTT[G/T]CTAACCTAATATGTA | 226747 |
rs222276789 | in-del | -/AAAGTA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179749405 | CCTAATTAACTATAC[-/AAAGTA]AAAGTAAAAGTAAAA | 226747 |
rs222292822 | in-del | -/GAAGG | | | intron-variant | Ahctf1 | Mm_Celera | 1:179772630 | GTGGTTACTATATAA[-/GAAGG]CTGGCCTGGGAGTAT | 226747 |
rs222311584 | snp | C/T | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805585 | ACTGAGGATGACAGT[C/T]AGGGCTGGGGTTACA | 226747 |
rs222387344 | snp | A/G | | | synonymous-codon, downstream-variant-500B | Ahctf1 | Mm_Celera | 1:179753254 | TCCTCTCCTAGGAGC[A/G]GGAGGACTCTGAGCT | 226747 |
rs222491598 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179761588 | GCAGGGCCAACCAGA[C/T]AAAGAGGAGTTGACC | 226747 |
rs222523535 | snp | C/T | | | missense | Ahctf1 | Mm_Celera | 1:179752449 | GCGTGAGAGCAGCGG[C/T]GGCAAGCAGTCCGTC | 226747 |
rs222561948 | snp | A/G | | | missense | Ahctf1 | Mm_Celera | 1:179753162 | AGCCTCAGTCTTCCC[A/G]GCGTACCCTGAGGTT | 226747 |
rs222573914 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179798742 | TAGAATTCACTGTCC[C/T]ATAAATTTACTAATA | 226747 |
rs222713201 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ahctf1, Gm1305 | GRCm38.p3 | 1:179746991 | AAATTAATGAAGAGG[C/T]AGACTATCTTCTCTT | 226747 |
rs222791318 | in-del | -/TAT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179776562 | ACAAACATTGGGATA[-/TAT]ATATAGGGATCAAGA | 226747 |
rs222901567 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179801786 | GTTAGGATCTTAGCC[C/T]GGCGTGGTGGCGCAC | 226747 |
rs222947500 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179790291 | CTTAGAAGCACAGGC[A/G]TACTGACCTATCTTG | 226747 |
rs222989361 | in-del | -/GA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792722 | CCCACATGATACAAG[-/GA]GAGAACCACCTCCTC | 226747 |
rs223002582 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179757779 | ACAAACAAACAAAAA[A/C]CCAAAAAAACCCCAA | 226747 |
rs223101563 | in-del | -/TTT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179798537 | CCCCTTATGAGGTTC[-/TTT]TTTTTTTTTTTTTTT | 226747 |
rs223185227 | in-del | -/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179748394 | TTAAATAATTTTTTT[-/C]CAACAAATTTACTTA | 226747 |
rs223187484 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179799674 | GGAATGTCCACATTT[A/T]GAGTTACCCCTTTTC | 226747 |
rs223198902 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179802829 | GACTCTCCAAAAAGT[C/G]AACCAAAGGCAAAAG | 226747 |
rs223345378 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179786451 | CTAAGTGCTAGGACT[A/G]AAGGTTTGTGCCACC | 226747 |
rs223375368 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179791160 | AAAAGGCAATGAGTA[A/T]GAAACTAAAGAGTTT | 226747 |
rs223503580 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179760180 | GGATTAAGGTGTGTA[C/T]TACCATTCCTAGCCT | 226747 |
rs223532136 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750390 | TCCGCCTCTCCCTTC[C/T]ATCATGCCAGTTTTT | 226747 |
rs223638637 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179783666 | CACAACTTTTTTTAA[A/T]AAAAATAAGTGATTA | 226747 |
rs223670388 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750827 | CCAGCCTGGTCTATA[A/G]AGGTAGTTCTAGGGC | 226747 |
rs223672326 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179757114 | GGGAACTGAATCCAG[A/G]AGCTCTGGGAGAGCA | 226747 |
rs223693186 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179787849 | GGAAAGAAAAAGACA[C/T]GGGGTGGGGTTTGGG | 226747 |
rs223741875 | snp | C/T | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805497 | TTGTGTGGTCTGGTT[C/T]TGTTTTGCTGGTAGT | 226747 |
rs223784720 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793543 | TTCCAGGACAGCTGG[G/T]GCCACACAGAGAAAC | 226747 |
rs223833188 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179794566 | TTAGAATGGATTAGA[A/T]GGATTAGGAGCCCTG | 226747 |
rs223861043 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793485 | CCACTTAAACATCAA[C/T]CCAGATCTCTTGAGT | 226747 |
rs223939553 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179777693 | GCTCCGTGTCACTGT[A/G]ACCTACGTGGATGCT | 226747 |
rs223977357 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179780757 | AAGACACAAAAACTA[A/G]AATGAAGACTAGTCA | 226747 |
rs223995047 | in-del | -/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750000 | GAAGGCCCAAACCTA[-/T]TTGTTCCATCAGGAG | 226747 |
rs223996583 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179798923 | GTATTTATTTTACTT[A/G]AGTGTGGGTGTGTTT | 226747 |
rs224001336 | in-del | -/AAAG | | | intron-variant | Ahctf1 | Mm_Celera | 1:179779724 | ATTAAAGTTGGAGAA[-/AAAG]AAAAAGTTAGCAATA | 226747 |
rs224040915 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179785748 | ACAGCCACTGTTATA[C/T]TGTGAGACCCCGCCC | 226747 |
rs224073774 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179786880 | GATTCTCCTGATCTA[A/G]AAGAAAAAGTTTTAA | 226747 |
rs224086531 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179778592 | CTTCCCAAGTTCACG[G/T]TCATTAGCCTCGAAT | 226747 |
rs224139025 | in-del | -/AAAC | | | intron-variant | Ahctf1 | Mm_Celera | 1:179757757 | CTGTACAAAAAACAA[-/AAAC]AAACAAACAAACAAA | 226747 |
rs224143722 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179789943 | CAGTAAGTGCTACCT[-/A]AAAACATCAACAGCA | 226747 |
rs224223148 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179751875 | TAACACGACAAAGAG[G/T]AACTAAGGTGTTTGT | 226747 |
rs224292351 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179759439 | GAGTATCTCCCTATA[A/T]TAACCAAGATTGACC | 226747 |
rs224328660 | in-del | -/CTT | | | cds-indel, downstream-variant-500B | Ahctf1 | Mm_Celera | 1:179753230 | GCCTTGGCTAACGTC[-/CTT]CTTCTTTCCTCTCCT | 226747 |
rs224406527 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179760100 | TAGCTGTCCTAAGCT[A/C]ACTCTGCAGACCAAG | 226747 |
rs224439437 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750360 | CACAGGCCAGGCTAC[C/T]TGGCTCACAAGCATT | 226747 |
rs224472560 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179749503 | TGAATATGATCACTG[C/T]TATGTACATACATAA | 226747 |
rs224473646 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179746060 | AACTCAAACAGAAAG[C/T]TCCTCTCAAAAATCT | 226747 |
rs224634024 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179747290 | AAAATATAAATTGCT[C/T]AAGCAATTAAGAGTT | 226747 |
rs224672602 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179753856 | CACCTTCTAAAATCA[A/G]GGTAAAGTTGCTCTG | 226747 |
rs224675150 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792771 | CTCAAATGTACACCA[C/T]GACATACATGTCCTC | 226747 |
rs224760277 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179777365 | AACCATCTGAGCATG[-/A]CCACTAACTCTGAGT | 226747 |
rs224802308 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179789273 | GTCAGTGCTCTTAAC[C/T]GCTGAGCCATCTCTC | 226747 |
rs224803802 | snp | A/G | | | downstream-variant-500B, intron-variant | Ahctf1, Gm1305 | Mm_Celera | 1:179744762 | GATGAGCTACCCTAG[A/G]GATTCATGCACGGTA | 226747 |
rs224841653 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179790788 | GTCATCACCGTTTGT[C/T]TGCTCTTTCAGAGTC | 226747 |
rs224868752 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179749714 | CTCCTTTAAACAGCA[C/G]TACCATAGCAGTGGC | 226747 |
rs224964845 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179786554 | TAAAAAACTCAAAAT[G/T]TATAAACATACTCTA | 226747 |
rs224975732 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179800964 | AAGGCTAAGAAACTT[-/A]AAAAAAAATACCATA | 226747 |
rs224991108 | snp | C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179750435 | GGATTCAATCTCAGG[C/T]CATCAAGGTTGAGAG | 226747 |
rs225002330 | in-del | -/TT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179799172 | CAAGTGCCTGAGCTC[-/TT]TAGTCTCAAATTAGT | 226747 |
rs225020229 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179745779 | AGTACTGGAAAATTA[C/T]TCATTTGAGGTAGAT | 226747 |
rs225021538 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750873 | GTGAAACCCTGTCAC[-/A]AAAAAAACAAAAAGG | 226747 |
rs225023112 | in-del | -/TTGGTTGTGATG | | | cds-indel, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179753779 | CACACAGGTTTTTCC[-/TTGGTTGTGATG]TTGGTCGCTTTCGGT | 226747 |
rs225160927 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179797327 | TTTATTCTCAGCTAT[A/G]CAAACTACCTACTTA | 226747 |
rs225193391 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179783663 | AATCACAACTTTTTT[A/T]AAAAAAAATAAGTGA | 226747 |
rs225251708 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179783125 | TGTAGGAGGAGCCAG[A/G]TAGGAAGGCCAAGTT | 226747 |
rs225274391 | snp | A/T | | | missense | Ahctf1 | Mm_Celera | 1:179753003 | GCTGCCTCACTCCCT[A/T]TGAGATCATCTAGAA | 226747 |
rs225643235 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179784460 | AATGAAGCTTAACTC[A/G]TCAGCTAAGGAAACT | 226747 |
rs225708292 | in-del | -/ACGG | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793007 | AAAGAGTCTTATTAA[-/ACGG]GCAGAGCTGGGGCTG | 226747 |
rs225716275 | in-del | -/CAC | | | intron-variant | Ahctf1 | Mm_Celera | 1:179790778 | TGGGAATTTGGTCAT[-/CAC]CGTTTGTTTGCTCTT | 226747 |
rs225722784 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179779399 | TTTACTTTTTTAGGA[A/G]ACTTTTGTGTTTTGT | 226747 |
rs225765751 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179769183 | TGCATCTCTCACATG[A/T]CTTTATTAATAGAAA | 226747 |
rs225815359 | in-del | -/AT | | | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179746019 | AGAAAGGATATGAAC[-/AT]ATGTCCAGTAGCATA | 226747 |
rs225954796 | in-del | -/AC | | | intron-variant | Ahctf1 | Mm_Celera | 1:179772028 | TGTCTCGAAAAACAA[-/AC]AAACAAAAACATAAA | 226747 |
rs225964221 | in-del | -/ACTT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179798277 | ATATGCAGGTAAAAC[-/ACTT]ACAAGCATAAATCTT | 226747 |
rs225985858 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179777162 | TGAGTAGCTTCCACT[C/T]TTTCCTTCCAGCGCT | 226747 |
rs226010226 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179781010 | TTCATTTATCAATCA[C/T]GAACAACAATCAAAA | 226747 |
rs226140457 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179771020 | GAATCAAAAGATAAT[C/T]ACACATGCAACTAAA | 226747 |
rs226245259 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179774241 | TCTGTGAACATGTGC[A/G]TATATGACACGTGTC | 226747 |
rs226364354 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179775876 | TTCTTGCTGTTTAGG[C/T]GAGAACACCAGTTAA | 226747 |
rs226382509 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179776438 | GTTTAGTAAATTTTT[A/T]AAAAGTTATAGATCA | 226747 |
rs226399447 | in-del | -/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179784959 | AGGTTACAGATTCCC[-/T]TCCCCCCAAAAAAAA | 226747 |
rs226495553 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179768673 | AGATGTTTGAAATGT[A/G]AACTTAATGACAAAA | 226747 |
rs226523736 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179766385 | GTGCGTGCGTGCATG[C/T]GTGCGCACGCGCGCT | 226747 |
rs226629955 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179759788 | GAGTTTACAGACAGC[C/T]GTGAAGCATCTCATA | 226747 |
rs226630079 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179769653 | CAAACTCTGATACTT[C/T]ACAACTCATACAATG | 226747 |
rs226646268 | in-del | -/GT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793151 | TCAGGCAAGCAGGAT[-/GT]ATATGCAACAGAGCA | 226747 |
rs226705259 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179748011 | GGAACTGAACTCAAG[A/G]GAGCCTATCTCTGCC | 226747 |
rs226793406 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805141 | AGGCAGAATCAGGAG[A/G]ATCTCTGTGCGTTCA | 226747 |
rs226825721 | snp | C/T | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805615 | AGGCATGCACCCCTT[C/T]CCCAGTTTTAGGTGG | 226747 |
rs226854089 | in-del | -/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179796290 | AAGTATCACCATTCC[-/T]TTTTTTGTCTCCGAA | 226747 |
rs226867858 | in-del | -/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179778020 | TAAGTGCAGTCACTA[-/C]CACACCAGCCGGTGA | 226747 |
rs226914848 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179772308 | TAATCTACATAAACA[C/T]CAGCAAAGCAATTGT | 226747 |
rs226960387 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179762392 | AAAGAAGGCAAGCCA[C/T]TTTCATAAGCTGACA | 226747 |
rs226982907 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179745875 | ATCAGGCAAAGCCCA[A/G]TGAGCACAGGTACTG | 226747 |
rs227154516 | in-del | -/TA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179788466 | TGAAGGCTATAAAGT[-/TA]TATATATATATAAAA | 226747 |
rs227432262 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179799897 | ATCTCTTCACAACTT[C/T]TGTTGTGAACCAAAA | 226747 |
rs227529486 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179802421 | ATATTTTCTTCTAAA[A/G]AATCCACGCTCTTTA | 226747 |
rs227593113 | in-del | -/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179784039 | CATACCCTCCCCCCC[-/T]ACTCCCCTACCCACC | 226747 |
rs227595116 | snp | A/T | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805933 | GACCTTTTGGGCGTT[A/T]GTTCGTTAATCATCT | 226747 |
rs227639542 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179780819 | ACACTATGGAGCTAG[A/G]ATGTCTGAATAGCTA | 226747 |
rs227678300 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179803709 | GATCGCAGATCGCGC[G/T]GCGGGGCTCGGACTT | 226747 |
rs227715567 | in-del | -/AACT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179767121 | TACATAAACAAAACA[-/AACT]GAAGCGATCATGTAA | 226747 |
rs227913294 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179797944 | AAAAACCAAAGCTGA[C/T]TGGGAAATGGAATAG | 226747 |
rs227932248 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179762079 | GACAATAGATTCACA[A/G]GCCCGAGGACATTCA | 226747 |
rs228040024 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179798887 | TATATACATTGCAAA[C/G]CAAATTGGTAATTTA | 226747 |
rs228127678 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179775622 | ATCACTAAAGTAAAA[A/T]TTAGATAAGTGTAAA | 226747 |
rs228229483 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179771750 | CTAACATGTGCTCAC[A/C]AGTTGGTGGTCCTCT | 226747 |
rs228331001 | snp | A/T | | | synonymous-codon, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179762573 | CACGGGTGAAGGAGC[A/T]CCTTCTGACTTAAAC | 226747 |
rs228466581 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764149 | AGAGTCAGCGGGGCC[A/G]ACTGCTCGGAGTAAG | 226747 |
rs228491974 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179768656 | TCACACCCACAAATA[A/C]AAGATGTTTGAAATG | 226747 |
rs228521707 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179761737 | AGAAACCCTGTCTTG[-/A]AAAAACAACAAAAAC | 226747 |
rs228550266 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179759508 | ATACCTAAACTAGAC[C/T]GTGTTTCAGACAGCA | 226747 |
rs228551075 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179759541 | CACTGATGGACATCA[A/C]CTTTGCTTTGCGGGT | 226747 |
rs228568332 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179762708 | TTCTGGTGATGGTGC[A/G]TCATGATACTCTAAG | 226747 |
rs228649852 | snp | C/T | | | intron-variant, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179754497 | TTCACCTACATAAGC[C/T]CCCTTGGGCTAGACT | 226747 |
rs228652536 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764768 | ACTACACAAGAAACT[G/T]AGAGGAGCTGGGCAC | 226747 |
rs228798561 | in-del | -/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179777324 | AGCCTAAAATAGTAA[-/T]TTTTATATACTTTTA | 226747 |
rs228809656 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179766343 | TGTACTGGCTGTTCT[A/C]GCCGTGTTTTATTTA | 226747 |
rs228811630 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179800202 | GGGGCAGAAGAAGAT[A/G]GACAGACAATAAGAA | 226747 |
rs228843306 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179801173 | TTTCTGAACTCCTGG[C/T]CTTAAACTCCGGCTT | 226747 |
rs228878387 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179757321 | AAGATTAAGTGAGCT[A/G]ATATATAAGAAATGT | 226747 |
rs228958780 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179768066 | TTAGTGGTCAACAAA[A/G]CAAAGTCTGACAGCT | 226747 |
rs228998882 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179758665 | TTCACAACTTGCCCA[A/C]TAACCAGCTTGTCCA | 226747 |
rs229008309 | in-del | -/AAT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179765341 | TGAAACAAGTGAGAA[-/AAT]AAGCCTAAAACCAAA | 226747 |
rs229023099 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179760994 | TTCATATTAACGTCT[A/G]TATTTGTTAAAGACA | 226747 |
rs229023394 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750563 | GCTGATGAGAGGCAG[A/G]CCTTACACTGCAGGC | 226747 |
rs229201648 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179794003 | AATTAAGCTATTAGT[C/T]AACATAATAAAATAT | 226747 |
rs229214343 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179804142 | CTCAAAAAGCAGAGA[A/G]TTCAGGTCGCCTAGC | 226747 |
rs229232432 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179795554 | ACTATATATTGAAGG[G/T]GATAATTACACAAAA | 226747 |
rs229275987 | in-del | -/ACAGAGG | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805976 | GGACTGACACAGAGC[-/ACAGAGG]ACTGACACAGAGCAC | 226747 |
rs229282646 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179802102 | CACCTGTAATCCCGG[C/T]TATTCCCTGGGCTGA | 226747 |
rs229369375 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179803956 | GCGGAGCAAGGGCCG[C/G]CCTAATCTAGTGGCG | 226747 |
rs229389716 | snp | C/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179804894 | AAGACCTGAACCACC[C/G]TTTCATTCTTTTAAC | 226747 |
rs229393272 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179751228 | AATAAAAGGTGCCTA[C/T]TCTAACACAGGAATC | 226747 |
rs229401093 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179791812 | ATTTGCTGCCTTTTC[C/T]AATATTACCTGCTGA | 226747 |
rs229510613 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792785 | ATGACATACATGTCC[C/T]CTTATACACATGTAT | 226747 |
rs229627499 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179801279 | GAAAGACAGACCCCA[A/G]TAGGCAGGGAAGATC | 226747 |
rs229710475 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179783412 | AGACCCCAAATCATG[C/G]TAGGCATAATGGCAC | 226747 |
rs229736610 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179784079 | CTATTTTTACAAAGT[A/G]AAACTGTTACCTTCT | 226747 |
rs229758770 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179761806 | AGGCAATTGGTTCAT[C/T]GATTCTAAACCAAGT | 226747 |
rs229907208 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179760789 | CTAGCGACTATCTAA[A/G]TATTTTAGTGGAATA | 226747 |
rs229964984 | snp | G/T | | | missense, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179753773 | CCTGTGGCACACAGG[G/T]TTTTCCTTGGTCGCT | 226747 |
rs230095373 | snp | C/T | | | synonymous-codon | Ahctf1 | Mm_Celera | 1:179752915 | GTCACTGTGTTCATC[C/T]TGTTTATACTCCATA | 226747 |
rs230124622 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179804974 | GACTGTATCATTTCT[A/G]GACTGTATCATTTCT | 226747 |
rs230164743 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179797518 | AGGCAAAGACATTCA[A/T]ATCTCAGAGTTCAAG | 226747 |
rs230172677 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792989 | TCTTTTCATTTTTCT[C/T]GAGAAAGAGTCTTAT | 226747 |
rs230187960 | in-del | -/TG | | | intron-variant | Ahctf1 | Mm_Celera | 1:179767825 | GTCTGGGATCCTCTC[-/TG]TAGAAAAGCTTGGCC | 226747 |
rs230224483 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179796567 | AAAAAATTATGCATA[C/T]ATCCTAAACTGGACA | 226747 |
rs230284062 | in-del | -/AAC | | | intron-variant | Ahctf1 | Mm_Celera | 1:179758947 | AATTACAAAATAAGG[-/AAC]AACAACAACAACAAC | 226747 |
rs230420096 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179747716 | TATAGGCATTGGGTC[A/C]CCAAAGGTGGCTTTC | 226747 |
rs230449998 | snp | C/G | | | synonymous-codon, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179793671 | TTCATTCTGACTGCA[C/G]GACAAGTCATCCAAA | 226747 |
rs230454589 | snp | G/T | | | missense | Ahctf1 | Mm_Celera | 1:179748672 | TCTTTCAGCTGGGCT[G/T]CGGCCTCCATGTTCT | 226747 |
rs230493248 | in-del | -/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179768926 | ACAGGCACCCTGACA[-/C]CCATGCCCTCCACTC | 226747 |
rs230524973 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179761127 | GGTGGTGGGATAGCA[A/C]AGTCTCAAATGTCCC | 226747 |
rs230542467 | in-del | -/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179756441 | GTTTACCAAAAAGTA[-/G]GTACAGCATAGAACA | 226747 |
rs230579799 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179791011 | ATGTGATACCAAGTG[C/T]GGTGGCCTGAATTCA | 226747 |
rs230590883 | in-del | -/CT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179747550 | CACAGAGCCCTCTGG[-/CT]CTCTGACAGAAACTT | 226747 |
rs230652238 | in-del | -/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179801591 | CGTTAAGCTGACATG[-/C]CTCAAAAGATGAGCA | 226747 |
rs230680018 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179801059 | TTCTAAACCTAGCCA[C/T]TAAATAAGTATCTGG | 226747 |
rs230710779 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179788556 | TTTTCTAAAACACGG[G/T]AGCATTCATACATTA | 226747 |
rs230761500 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179745519 | TTAAAACCTGAATAC[C/T]AGAGAGGCTCCTGTG | 226747 |
rs230823447 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179800014 | GGCTCACAACCACCA[A/G]CATAACTCCAGTTCC | 226747 |
rs230878523 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179787295 | CATCAGAAGGTTCTC[C/T]CTTTACTAGTTTCCA | 226747 |
rs230886071 | in-del | -/T | | | utr-variant-3-prime, intron-variant | Ahctf1, Gm1305 | Mm_Celera | 1:179744906 | TATTTCTCTTGTCAG[-/T]TTTTTTTTATTGTGC | 226747 |
rs230888197 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179786366 | GTTTCTCTGTGTAGC[C/G]TTGGCTGCCCTGGAA | 226747 |
rs230896303 | in-del | -/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179799786 | TTCTGTAAAAATGAA[-/G]AAAACTCCATAATGT | 226747 |
rs231063581 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179762810 | ATGGGTAGCCAGTGA[C/T]TCTGCCACCACTTTC | 226747 |
rs231064283 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179777036 | TCGTGCTCCTATAAC[A/G]AGCACTTTACCTACT | 226747 |
rs231099506 | snp | C/T | | | missense, downstream-variant-500B | Ahctf1 | Mm_Celera | 1:179753538 | TGGACGAATGTGCAG[C/T]CTTTGAGACTATCAC | 226747 |
rs231191503 | in-del | -/GCCA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179797734 | CTATTCCATTAGGAC[-/GCCA]GCCAGCCAGCCAGGA | 226747 |
rs231225375 | in-del | -/TTTTTA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179798840 | TTTTTTTTTTTTTTT[-/TTTTTA]AAGGAACATATATCT | 226747 |
rs231263381 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179799119 | TATGCATATCTATGT[A/G]TAGTGCAATTAAGCT | 226747 |
rs231345057 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179781521 | CCCTACATATACACA[C/T]ATAAGTTAAATTTTT | 226747 |
rs231386356 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179771252 | CTCTGCATTCCCAGT[A/G]CTGGGATTAAAGGCC | 226747 |
rs231408405 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179772089 | ACCACACCCCCAGCT[A/G]TGACGATTCTCTGCA | 226747 |
rs231416804 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179763990 | AGTGGTTAAGAGCAC[C/T]AACAGCTCTTCCAGA | 226747 |
rs231453107 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179754438 | AAATTACCTAACTAT[C/G]CACACTTTCTAAACA | 226747 |
rs231513739 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750530 | GAGCATTAGCAGCAC[A/G]AGACACCCTCCCCAC | 226747 |
rs231677698 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179779708 | ATCATCTGGAGGTTT[G/T]ATTAAAGTTGGAGAA | 226747 |
rs231686424 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179758286 | AAGTACAAGTAAAAT[A/G]ATGTTTAAGTGCCTT | 226747 |
rs231725106 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179748191 | CCTTGCTTAAAATAT[G/T]TATTATTTTTATTTC | 226747 |
rs231904634 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179778046 | GGTGAAGGAAAGAAC[A/C]GGACCAACCCAGCAA | 226747 |
rs231961683 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179779150 | TACTCTGTCCTTTGT[A/G]TACTGGAAGGCTAGT | 226747 |
rs231972112 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179791657 | GCATGCCGTACACCC[A/G]GAGGGGTACCCAAGA | 226747 |
rs231981553 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179751102 | ACACAGCTCTCTGGG[A/G]AGAAGGAGAGGTAGC | 226747 |
rs232007791 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179778719 | GTGAACCATACCCTA[A/C]ATGTTACTTGGTCTT | 226747 |
rs232179219 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179747358 | TGTAGCCCTGGAACT[A/C]ATTTTGTAGACCAGA | 226747 |
rs232463107 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179773738 | GTAGAAAGAGGAAAA[A/G]AAAGGAAATAATAGC | 226747 |
rs232492195 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793902 | GCAGGTTAGTAACTT[A/G]AACAGTCTTAAATAA | 226747 |
rs232500685 | snp | A/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179790876 | TAATCCTCCTCCTCC[A/T]CCTCCATCTCTCCAC | 226747 |
rs232500829 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179774805 | GCACTTACATAGCCA[A/G]TGATTGATGATGGTG | 226747 |
rs232528809 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179781120 | TGTTAAGATAACTGA[C/G]AGAAATAGGCATTTT | 226747 |
rs232540208 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764393 | GGGTAGCCAGGGCTT[C/T]ACAGAGAAACCCTGC | 226747 |
rs232592008 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764959 | AGTGGTTAAGAGAAC[C/T]GACTGCTCTTCGGGA | 226747 |
rs232738921 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179802849 | AAAGGCAAAAGTCAT[C/G]GGCCTTACAGCTCGC | 226747 |
rs232769425 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179804486 | CAACTGTAGTGGACC[A/G]ATCAACCATCCATCC | 226747 |
rs232924311 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179777490 | AAATACTTAGTAAAA[G/T]TTTAAAGGATACAAT | 226747 |
rs232964376 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179767979 | CAACTATTACTGCAC[C/G]TAAGCAACACAAGAC | 226747 |
rs233014561 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179776235 | GCAGGATGTAGAATG[A/G]AGAGGTTTAAGAAAC | 226747 |
rs233040954 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179785493 | GCACATGCCTTTAAT[C/T]CCAGCACTTGGGAGG | 226747 |
rs233093621 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179774328 | TTCATCAGGCATGCA[C/T]GACAGACACTTTTGC | 226747 |
rs233143096 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179775549 | AGTGTTAACTATAAA[C/T]ACAGTCTTTAGTATT | 226747 |
rs233169906 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179777885 | TTAATAACAAAACAG[G/T]AAGCATCAAATGCTT | 226747 |
rs233177676 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179767129 | CAAAACAAACTGAAG[C/T]GATCATGTAAGCCTG | 226747 |
rs233209956 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179768092 | CAGCTTGTTTTCCTC[A/G]GGGTTTTAATATGGC | 226747 |
rs233216614 | in-del | -/A | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179757780 | AAACAAACAAAAAAC[-/A]CAAAAAAACCCCAAA | 226747 |
rs233320722 | in-del | -/TT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179751820 | TCTGTAATAGATGTA[-/TT]TTTTTTTTAACAGAA | 226747 |
rs233332605 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179782156 | CAAATCACCTTACAA[C/T]ACAAGGTCTCCATTA | 226747 |
rs233498195 | in-del | -/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179784630 | TGTGGCCAGACCAAC[-/T]TTTGATCTTGCTAGC | 226747 |
rs233537070 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179762241 | TACTTGTCATAGTTA[C/T]TGGATGTGTTCAGGC | 226747 |
rs233569456 | snp | G/T | | | missense | Ahctf1 | Mm_Celera | 1:179753064 | TCTTAAGTCTTCTAG[G/T]GGTTCCCTTTCTAAC | 226747 |
rs233654641 | in-del | -/TC | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179804739 | TAACAGTTCTTTTTT[-/TC]TTTTTTTTTCCTTTC | 226747 |
rs233656764 | in-del | -/AATAA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793356 | GTATATCAACACACC[-/AATAA]AATAAAATAAAATAA | 226747 |
rs233732293 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179788902 | TGCCTGCCTTTGCCA[A/G]GATTAAAGGCCATGT | 226747 |
rs233782991 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805712 | CCATCCCTCTTTCTT[A/G]TGAACTAATTTTCTG | 226747 |
rs233887834 | in-del | -/AC | | | intron-variant | Ahctf1 | Mm_Celera | 1:179751087 | AAATCCAGGGCTGGA[-/AC]ACAGCTCTCTGGGGA | 226747 |
rs234084336 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179748470 | AGCCTGAGGCAAGAT[C/T]ATGACTTCTAGACAA | 226747 |
rs234209477 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179779896 | CTGTCCTTGAACTTG[C/T]TCTGTAGACCAGGCC | 226747 |
rs234379959 | snp | G/T | | | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179745923 | CAGCATCAAAGTGCA[G/T]ACATTATAAAACAGC | 226747 |
rs234442083 | snp | A/T | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805843 | CCTTCCATATCAGAC[A/T]CCTTGGTAGTAAGAA | 226747 |
rs234482109 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179794528 | CACACATTTCAATGT[C/T]TAGTCACCAGGCAGC | 226747 |
rs234494368 | in-del | -/TAT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179774618 | TTCCCCAAATATAAC[-/TAT]TATGGTTCAAGGACA | 226747 |
rs234521983 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179796148 | ACAGTTAGTTAACAC[A/G]AGTACATACAAGCAG | 226747 |
rs234543819 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179798425 | CCTTTCAAATTTACC[G/T]CCTCCTAGCAATTCT | 226747 |
rs234544966 | snp | G/T | | | missense, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179770599 | CATACCATGAGATTA[G/T]TCTTCAGAATCTGGT | 226747 |
rs234640720 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764305 | TCTTAAAAAGCCACA[A/C]GCCTTTGATCCCAGC | 226747 |
rs234649235 | in-del | -/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179769719 | CTGAGTGAACATGTG[-/T]TGCTGACATGGCCAT | 226747 |
rs234689905 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179799427 | GATGAATCTGAGGGA[A/G]AGCGAGCCCCATTCA | 226747 |
rs234809073 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179749922 | AAGAGAGACAGACAC[A/G]CAAATAGACAGATGA | 226747 |
rs234902510 | snp | G/T | | | synonymous-codon, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179769078 | GATGAACGTAGATCG[G/T]GTTAACACTGTTCCA | 226747 |
rs234924094 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179804544 | AAGTAGGTCAGGGAG[A/G]TTTTAGAGGTTTTAC | 226747 |
rs234940551 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179770321 | CTAATTTCTGAAGGT[C/T]TGCTCTTTGGGCTGT | 226747 |
rs234964010 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792617 | TTCAATTCCTACACT[C/T]CACATAAAGGTGTAT | 226747 |
rs235114204 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793190 | ATTAAAGTTTAAAAA[A/T]ATTTTTGCTAAAAGT | 226747 |
rs235190889 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179781127 | ATAACTGAGAGAAAT[A/T]GGCATTTTATGCAAA | 226747 |
rs235201607 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179797496 | ACCTTTAGTCCCAGT[-/A]CTCAGAAGGCAAAGA | 226747 |
rs235241965 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179779073 | CTTTCTTGATGGAGT[A/G]CCCCAAGATACTGTG | 226747 |
rs235256092 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179757673 | TGCTCATGGCCAGCT[C/T]CTACTTCTCTACTCT | 226747 |
rs235298844 | in-del | -/CTAA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179773836 | AATACTAACAGTTTC[-/CTAA]CTATTGTGCACCCAC | 226747 |
rs235303803 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764562 | ACCTAACAAATACAT[C/G]AAGCTCTTTTAAACT | 226747 |
rs235345520 | in-del | -/AGGCTC | | | intron-variant | Ahctf1 | Mm_Celera | 1:179794628 | TTAAAAGCACATGAT[-/AGGCTC]AGGTTCTGTCCCTGT | 226747 |
rs235362083 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179756775 | TCTTCCCAAAGCACA[A/G]CACAGACCCAAGAAG | 226747 |
rs235410372 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179802708 | CATGTGTGAGGACCT[A/G]GATGTGATTCTTCAC | 226747 |
rs235504589 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179758787 | AGAGGAAACAAACAA[C/T]AAATGAAAAAAGAAA | 226747 |
rs235525606 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179759828 | GGTAGGAATAGAACC[A/T]GGGAACTTTGAAAGA | 226747 |
rs235596940 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179800434 | TTAAGGTCTAGATGA[A/G]CCAGTGACGTACAGC | 226747 |
rs235702288 | snp | C/T | | | missense | Ahctf1 | Mm_Celera | 1:179752476 | CGTCCCTTCGGTCAG[C/T]GGACTCTGTGTGGGC | 226747 |
rs235732415 | snp | A/G | | | missense | Ahctf1 | Mm_Celera | 1:179753180 | GTACCCTGAGGTTCC[A/G]GCTCCGGCTCCACAG | 226747 |
rs235764547 | in-del | -/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179766748 | GGAAAAGTAACCAGC[-/T]TTTGCTGCTGCCAGA | 226747 |
rs235896581 | snp | C/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805423 | AAGTGTGCTAGTTTG[C/G]GCAAGGTATTATTCT | 226747 |
rs235927326 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793419 | AGCCAAGAGGACTAG[A/G]ATGCCTAGGTACACA | 226747 |
rs236028988 | snp | C/T | | | missense, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179763489 | TCAGTCCAGTGTGTA[C/T]TCATGCCTTCTTCCA | 226747 |
rs236241252 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179765702 | AGAGAAAATGTATTG[-/A]AAAAAATTGAAAATG | 226747 |
rs236241427 | in-del | -/CAT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179768639 | GCCTCTGATCTCCAC[-/CAT]ATCACACCCACAAAT | 226747 |
rs236277217 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179771187 | CCACTCTAGCTGTTA[C/T]GGAATTTACTATGTA | 226747 |
rs236418048 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179760001 | TTCTTAGAATTGAAT[G/T]TGGATCCTCTGGAAG | 226747 |
rs236471843 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179761381 | ACTCGCTCAATAAAA[A/T]TTTAATAACATGGGC | 226747 |
rs236508255 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179789979 | TACCTTCCTTTGCAC[C/T]AAGTCCTGGCCAAGA | 226747 |
rs236510902 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179802482 | AAAGCACCCAAACTC[A/T]GCGACTTGGTTAGAT | 226747 |
rs236549648 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179790915 | ACATCATGGCTCTTA[G/T]CTTTGCCCAGCTATC | 226747 |
rs236556537 | in-del | -/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179751952 | TTTGGCTCAGAAGAC[-/T]TTTTTTTTTAAAATA | 226747 |
rs236784218 | snp | A/C | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179756957 | ATGTGGTAGTCCTGG[A/C]TATACTAGAGTTGTC | 226747 |
rs236806726 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179783667 | ACAACTTTTTTTAAA[A/T]AAAATAAGTGATTAT | 226747 |
rs236835658 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179791915 | TTCAATAATTGGTTT[-/A]AAAAAAATACCAAGA | 226747 |
rs236845981 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179784919 | AAGCCAAATTTCAAG[A/G]CCATGGCTACTGATC | 226747 |
rs237007535 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179746593 | TCAAGTGCTTCTCTC[A/G]CAGAGACCTGGAGAG | 226747 |
rs237211127 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179778642 | GAACTCCAACATTCA[A/G]TGTATTAGCATTACA | 226747 |
rs237293649 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179769540 | AATTTTAATTATGAA[C/T]GTCATCTAGTATCTT | 226747 |
rs237295376 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179778148 | TTCCAGCTCAGAGCT[-/A]AATCCTGGTTTTGTT | 226747 |
rs237305596 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179797241 | TCCTGTTTATGAGAA[C/T]AGCAAAACAAGACAC | 226747 |
rs237381391 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750838 | TATAGAGGTAGTTCT[A/G]GGGCAGTCAAAGTTA | 226747 |
rs237388784 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179799568 | AGCTAAGGATATTCT[G/T]TATTCCCACATTCTG | 226747 |
rs237484263 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179770476 | GATCCTTCAAGTTCA[C/G]GACAATGTAAACTAA | 226747 |
rs237496193 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179758711 | AGGCAGAAGCAGGCA[C/G]ATCTCTGAATCTGAG | 226747 |
rs237546935 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179765498 | ACAATCATATACAGA[C/T]GTGCATTATTTTTTA | 226747 |
rs237574449 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793546 | CAGGACAGCTGGGGC[C/G]ACACAGAGAAACATT | 226747 |
rs237610342 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179794677 | CTGGGAATCAGGATA[A/C]AGCTCTCAGGTACTT | 226747 |
rs237610665 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179780850 | TTCATACATTAACTA[C/T]GTTACCTAAGCCTTC | 226747 |
rs237650277 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179748768 | AAGGCAATCAATATA[C/T]AGCAGCAAAAATCCT | 226747 |
rs237664278 | in-del | -/TAAA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179762002 | CACACATAAAATACT[-/TAAA]TAGACAATCCCCATC | 226747 |
rs237688787 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179745859 | TCAAATTCAACACAG[C/T]ATCAGGCAAAGCCCA | 226747 |
rs237737059 | snp | A/C | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805819 | ATTCCCATCCTTTGG[A/C]ACAAATTTCCTTCCA | 226747 |
rs237772719 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179748158 | ACAGGGTTGGGCCTT[C/T]GATATAAATGTAAGT | 226747 |
rs237810667 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179749484 | AAAGGGTAGGGAGGA[C/G]AGCTGAATATGATCA | 226747 |
rs237819418 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792315 | TAAAAGAATTGATTA[A/G]TCAACAACTAAGAGA | 226747 |
rs237826422 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179746894 | CACAGCCTGAGAGTC[C/T]TGCTACACAAAGGCA | 226747 |
rs237860228 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179779277 | TTTCATATCATCTGC[A/T]AGGCCCTATGCCCAG | 226747 |
rs237875347 | in-del | -/AAACACACTG | | | intron-variant | Ahctf1 | Mm_Celera | 1:179770045 | CTGTTTCAACTGTAT[-/AAACACACTG]AGAATAAACACACTG | 226747 |
rs237967104 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179788436 | CACACAAATGCTTTT[A/G]GAGAGCAAATCGCTC | 226747 |
rs237994172 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179802460 | CTCCAACTGTCTATT[-/A]AAAAAAAAAGCACCC | 226747 |
rs238001459 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179776718 | TAAAAACTCGTTTGT[C/T]GTGTGTGGGTATGCT | 226747 |
rs238001472 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179790288 | ATTCTTAGAAGCACA[A/G]GCATACTGACCTATC | 226747 |
rs238035925 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179777293 | GATAAAAGGTAAGGT[C/T]ACCCCAAGAATAAAT | 226747 |
rs238057919 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179789770 | CAAGAAACCAAAACA[A/T]GCAGCTTACATCTCA | 226747 |
rs238082301 | in-del | -/C | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179804668 | GCAATAAACGCCTTT[-/C]TTAACTGCTAATTCT | 226747 |
rs238228168 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792044 | GCAAATGGGTCATCA[A/C]ATTGACTGTAATGCT | 226747 |
rs238261497 | in-del | -/AA | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179760711 | TCCAAGATTTCTATT[-/AA]GTCTCAACAGCTTAA | 226747 |
rs238266603 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179768511 | CTCCTCCTCACTTTG[C/T]GTATCTCTCTGCACT | 226747 |
rs238342013 | in-del | -/CTAA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179767487 | CATATTAGAAACCAT[-/CTAA]CTAAATGCAGTCCAA | 226747 |
rs238422699 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179781619 | TAAAATTTAATAAAA[C/T]ACTCATTTGTATAAA | 226747 |
rs238560035 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179760572 | AATTCTCAACATCCA[A/C]GGAGGTAGGTGAAAA | 226747 |
rs238583567 | in-del | -/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179791354 | GTACACTCAGAGGGG[-/T]TACCCAAGAGAGCAT | 226747 |
rs238604060 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750657 | CTACCTGGAGCAACA[C/T]CCATCATCTTTGGCT | 226747 |
rs238643596 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179773415 | AAAAGAATAAAACCA[C/T]ATAACAAAACAGCCC | 226747 |
rs238882455 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179801101 | CAGTCTTTCACTTGT[A/G]ATCCAAACAACCACA | 226747 |
rs238892917 | snp | C/G | | | missense, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179755478 | TATCAGAAGGAGCAG[C/G]AGAAATTCGAGGGCT | 226747 |
rs238931638 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179801798 | GCCTGGCGTGGTGGC[A/G]CACGCTTTTAATCCC | 226747 |
rs238977307 | snp | A/C | | | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179745624 | TCGGTGCACTGTTTT[A/C]TTTCTTTCTTCAATC | 226747 |
rs239174644 | snp | A/G | | | synonymous-codon | Ahctf1 | GRCm38.p3 | 1:179752947 | TCTGAGTATCTTCTA[A/G]ATTGGCATTCCTCAG | 226747 |
rs239205231 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179775957 | TAACGTAGTTATACA[C/T]GTTCTAGTATAATAA | 226747 |
rs239339551 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179774288 | CCAGACTCTGAAGTC[A/G]CCTTCCTGCCTCTGT | 226747 |
rs239372829 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179775269 | ATTTTTTTTTACTAT[A/C]TATTCCATCAATTCC | 226747 |
rs239391025 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179798253 | TGTATCCATATGGTA[C/T]ACATGCAAATATGCA | 226747 |
rs239415645 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764763 | ATATTACTACACAAG[A/G]AACTTAGAGGAGCTG | 226747 |
rs239461217 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179747486 | TACTGATTAAAAAAG[C/T]ACCCTGCTCAGACAA | 226747 |
rs239546591 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179765851 | AACAGTGCTGACTCC[C/G]TAGGGTACTAGGCAG | 226747 |
rs239738413 | snp | C/T | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179749759 | TGCAGAGATTACACT[C/T]GGGACTCTGAACTCA | 226747 |
rs239745440 | in-del | -/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179790268 | TCCTCAGCCTTAGGA[-/G]ATGAATTCTTAGAAG | 226747 |
rs239766817 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179770497 | TGTAAACTAAGATGG[C/T]TATGAGACTGTAAGT | 226747 |
rs239803675 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179771544 | AAACCAAGATCTAAG[A/T]GGAAAACGTGGATAA | 226747 |
rs239803791 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179760940 | AATTCTAGACACAAT[A/T]TTTTTTAATTTATGA | 226747 |
rs239868108 | in-del | -/AAC | | | intron-variant | Ahctf1 | Mm_Celera | 1:179752228 | TAAATAATTAACTAA[-/AAC]AACAACAACAACAAC | 226747 |
rs239879620 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179787543 | CACCAGAAGGGGCCT[C/T]GGCAGGAAGAGAAAA | 226747 |
rs239943362 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793169 | TATGCAACAGAGCAC[G/T]CATACATTAAAGTTT | 226747 |
rs239944809 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179761555 | ATCTTTAGGCCGGAG[A/C]GAGCAGGGACTGTGC | 226747 |
rs239990836 | in-del | -/AT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179801377 | AAAGCTACAATAGAG[-/AT]ATATATACACTGTGA | 226747 |
rs240023518 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179782134 | AAAAAAAAACAAAAT[A/C]AAAACCCAAATCACC | 226747 |
rs240107892 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179772564 | AGACTGGAAAGGTAC[A/T]TAGGGTGCAAATAAC | 226747 |
rs240140874 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179787882 | AACACAGCATGGTTC[A/G]AAAAGGAAAACAAAA | 226747 |
rs240269924 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179780551 | CAGGTCAGACAGGGA[C/T]ACATGGTAAGACCCT | 226747 |
rs240403725 | in-del | -/TT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179794158 | GAAACTTAAAACAAA[-/TT]TAAAAAAATCATAAA | 226747 |
rs240468179 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179757781 | AAACAAACAAAAAAC[A/C]AAAAAAACCCCAAAA | 226747 |
rs240472576 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179767879 | CTTCTGCTTCCCAAG[A/T]GCTGAGATTAAAGGC | 226747 |
rs240552930 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179768191 | TAAAATGATTATACT[A/C]CCAAAGTAGAACAGA | 226747 |
rs240714822 | in-del | -/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179775812 | AGTCAGTGCTGCACC[-/G]TGAATGACCCATTCT | 226747 |
rs240726148 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179783331 | CAGTCCAAACCAACA[A/G]CAAAAAAGGCCTACA | 226747 |
rs240881732 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179771088 | AGTCTTGCTAATGCC[-/A]AAAAAGACATCTGGG | 226747 |
rs240928158 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179772233 | AGGTTTACTCTTGCT[A/T]AACTATGAAAACTAA | 226747 |
rs240938725 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179795390 | CCAATGATGCAAGCC[C/T]GACAACCTGTATTTG | 226747 |
rs241052912 | in-del | -/TGCGTGCA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179766375 | GAGTGCGTGCGTGCG[-/TGCGTGCA]TGCGTGCGCACGCGC | 226747 |
rs241059671 | in-del | -/TT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179774474 | TCAGAGAAGAGGTTA[-/TT]TTTTTTGTATGTTTG | 226747 |
rs241254636 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179802071 | ACATTTTACTACTAA[A/G]TTACTATGTGGTTCC | 226747 |
rs241279216 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179790655 | CTGCTAAATCACATG[A/T]GTACAGCTATATTAT | 226747 |
rs241281112 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ahctf1 | GRCm38.p3 | 1:179803337 | CGGCGCGCGGGCCTG[C/T]GGTTCCCCACCCTAC | 226747 |
rs241318487 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179791292 | AAAAGCAAAGCCAAT[C/T]AAGGTTACAATGAAA | 226747 |
rs241324294 | in-del | -/GA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179799923 | CAAAAAGGAGGAATG[-/GA]GAGAGAGCTCAGTCG | 226747 |
rs241366577 | snp | G/T | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179804910 | TTTCATTCTTTTAAC[G/T]ATCAGTGAAAACAGA | 226747 |
rs241378863 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179759456 | AACCAAGATTGACCT[A/G]AAACTCACATTCCTC | 226747 |
rs241407504 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179760128 | AAGCTGGCCCTGAAA[A/T]CGTAGAGATCTGCCT | 226747 |
rs241464840 | in-del | -/TAT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179801633 | ACACCTTTTCAAGAA[-/TAT]TATGAGCCCAGGGCT | 226747 |
rs241505090 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179803907 | TCCCATAGGGCTTTG[C/T]GCGCTGGGCGTAGTG | 226747 |
rs241544977 | snp | C/T | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179804806 | CTGGCTATCTTGGAA[C/T]TCTCTTAGTAGATGG | 226747 |
rs241563507 | snp | G/T | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805490 | GTAAGTGTTGTGTGG[G/T]CTGGTTCTGTTTTGC | 226747 |
rs241565533 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179751549 | ATTCAGCCAAATGCT[G/T]AGTTCCAGATTCACT | 226747 |
rs241618394 | in-del | -/TTTTTT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179789111 | ATAATAACACTCCTC[-/TTTTTT]TTTTTTTTTAAGATT | 226747 |
rs241660872 | snp | A/G | | | missense, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179753903 | CCGTCTACTTCAGCA[A/G]CATCACATTCAGCAG | 226747 |
rs241713049 | in-del | -/TTAATA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179767606 | TGTAAAAACTCAATT[-/TTAATA]TTAATAAGTATAATT | 226747 |
rs241762987 | in-del | -/AAAC | | | intron-variant | Ahctf1 | Mm_Celera | 1:179748706 | CTAAAGACAAGCAGG[-/AAAC]AAACAAAACATCGAC | 226747 |
rs241780829 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179747158 | CAGGGGATGAACGGA[A/G]GATGGGGCTAGTGCT | 226747 |
rs241780868 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179757885 | GAAAAGAAAAATCTA[A/G]TAATAATACTCTTTT | 226747 |
rs241883171 | snp | A/T | | | intron-variant, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179746862 | ATTTGTACTTTCATT[A/T]GTCAGCCAAGCCTAA | 226747 |
rs241912468 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179799767 | AACCCTATAATGTTA[A/G]TTTTTCTGTAAAAAT | 226747 |
rs241947348 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179800877 | TAAATTTTAAGATAT[A/C]ATTTTAAATCCCTCA | 226747 |
rs241949199 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179786647 | AACATACAGCTGACA[C/T]ACTACATTTACACAT | 226747 |
rs241985028 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179788134 | TATTAATTCCAGAAA[C/T]CTGACATAAATCTTA | 226747 |
rs242034821 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179800996 | ACCAGTTTATGAAGT[A/G]AAATGCACAGTCCCA | 226747 |
rs242047006 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750615 | CCTACTGTTAACAAT[A/G]CAAGTCTATATTCAC | 226747 |
rs242131530 | in-del | -/AA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179763916 | AACAAAACAAAAAAC[-/AA]AAAAAACAAAACCAA | 226747 |
rs242207817 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179794074 | GTCATTTGCTTAGCT[A/G]GCTCATTTTATTTAT | 226747 |
rs242245637 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179795618 | TTTTAAGGTGAGCAC[A/T]TCTTGTGAGCTTTCA | 226747 |
rs242245699 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179781189 | TAAAACAGACTGAAA[A/G]TAGACTATTCAAATT | 226747 |
rs242315046 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179798657 | CTTGCCTCTGCCTCC[C/T]GAGTGCTGGGATTAA | 226747 |
rs242332404 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179781174 | ATGCAAAATGCTATT[-/A]AAAACAGACTGAAAG | 226747 |
rs242344235 | snp | A/C | | | missense, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179762590 | CTTCTGACTTAAACG[A/C]ATCTTTATCATTATC | 226747 |
rs242404430 | in-del | -/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179794766 | GAGACTGTAAGCAAG[-/C]CCCCCCCAATTACAT | 226747 |
rs242496406 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179786256 | GGTCTTACTGTGCAC[C/T]CCTGGCTGCCTTAGA | 226747 |
rs242598954 | in-del | -/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793189 | ATTAAAGTTTAAAAA[-/T]AATTTTTGCTAAAAG | 226747 |
rs242615243 | in-del | -/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179748362 | TAGTACAGTTAACTG[-/C]TGAGCCCACCTGCAT | 226747 |
rs242636828 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179755948 | TCTTGCCATTATTGT[C/T]AAAGTTTACCATAAT | 226747 |
rs242735589 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179791408 | CCAAGAGAGCATGCC[A/G]GTACACCCGGAGGGG | 226747 |
rs242798046 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805256 | ACAAACAGAAGGGGG[A/G]AGAGAGAAGGAGAAG | 226747 |
rs242849746 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179763425 | TTCAAGACTATCCAC[-/A]AAAGTTCATTAAAAA | 226747 |
rs243056519 | in-del | -/T | | | frameshift-variant | Ahctf1 | Mm_Celera | 1:179752564 | AGACTTCTTTGTAGG[-/T]CTCCTCTTAGATGTC | 226747 |
rs243094403 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750471 | TGCTTTACTGACTGA[A/G]TCACCTCCCTAGCCC | 226747 |
rs243134829 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179783067 | AGAAAGGAAAAAGAA[A/G]AAAAAGAATGATTAC | 226747 |
rs243225643 | in-del | -/CG | | | downstream-variant-500B, intron-variant | Ahctf1, Gm1305 | Mm_Celera | 1:179744572 | TGTTGGGATCACTGA[-/CG]CGTGTCCACATGTGG | 226747 |
rs243241996 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179777175 | CTCTTTCCTTCCAGC[A/G]CTGGAGATCAAACCT | 226747 |
rs243319746 | snp | G/T | | | missense, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179758011 | AACTGACGTCTTGGA[G/T]TTTGAAGTGGAGGTT | 226747 |
rs243378775 | in-del | -/AAGG | | | intron-variant | Ahctf1 | Mm_Celera | 1:179800745 | TTTGCAATTAGAAAA[-/AAGG]AAGACTGAGATTTTC | 226747 |
rs243493635 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179768832 | TTAAAAAAACAAACA[A/C]TTGTTGCCTCCGTTT | 226747 |
rs243507489 | snp | C/T | | | missense, nc-transcript-variant | Ahctf1 | GRCm38.p3 | 1:179777768 | ACTTCTCAACTTCAT[C/T]TCCTAGTTGAGAGAC | 226747 |
rs243543595 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179803576 | CCCCGCTGGCGACTC[A/G]ACTTACTGGGCTGGC | 226747 |
rs243573639 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179802483 | AAGCACCCAAACTCA[A/G]CGACTTGGTTAGATC | 226747 |
rs243650362 | in-del | -/CCT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792731 | ACAAGGAGAGAACCA[-/CCT]CCTCCTCCAAGTTGT | 226747 |
rs243653223 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179791955 | TGGTTGCCTTTAATA[A/G]ATTAGAGGGAGCAGA | 226747 |
rs243660901 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179771652 | CTTAGGTGTCCTGGC[A/G]TCAGTCTGGGAATCT | 226747 |
rs243708002 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179761604 | AAAGAGGAGTTGACC[G/T]GAGCGAGCAGAGGTC | 226747 |
rs243785699 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792788 | ACATACATGTCCTCT[C/T]ATACACATGTATACA | 226747 |
rs243787358 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179779110 | GAGGCTACTGTGAAA[G/T]GCACTGTTTCCTCAG | 226747 |
rs243820463 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179779932 | CTGCCTCCCAAGTGC[G/T]GAGATTAAAGGTGTG | 226747 |
rs243923992 | snp | A/T | | | downstream-variant-500B, intron-variant | Ahctf1, Gm1305 | Mm_Celera | 1:179744671 | CATAGCCAAGGATAA[A/T]AACTGAGCTTCTAGT | 226747 |
rs243947634 | snp | A/T | | | missense, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179746454 | GTCTTTATTTCATCC[A/T]CTGGACTCGCCAAGG | 226747 |
rs244025339 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179755761 | GACTTACCTAGACTT[-/A]AAGAGTTTTATCTTA | 226747 |
rs244100580 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179789607 | CAGTACAATAAAAAA[A/C]CACCAAATAGAAAAA | 226747 |
rs244135741 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179777057 | TTTACCTACTTAGCT[A/G]TCTCTCCAGTTCCTT | 226747 |
rs244147601 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179786959 | GGTGAGAAAACATAG[A/T]AATCATACCTTAAAG | 226747 |
rs244156920 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179774635 | ATGGTTCAAGGACAC[A/T]GAGAATAAACACTTG | 226747 |
rs244182736 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179775749 | CATGCCCATTAACTA[A/G]TTTTGTCTTCTCTGG | 226747 |
rs244234900 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805586 | CTGAGGATGACAGTC[A/G]GGGCTGGGGTTACAG | 226747 |
rs244275480 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Ahctf1 | Mm_Celera | 1:179793779 | TAAATGCTGGGTACT[C/T]GCACTGGCTCCTCCA | 226747 |
rs244358469 | in-del | -/A | | | intron-variant | Ahctf1 | Mm_Celera | 1:179755925 | GCTTCTCCAAATTGG[-/A]ATACAATTCTTGCCA | 226747 |
rs244363406 | snp | A/T | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805536 | TGTGTGAAGACTGTC[A/T]CATGTGCACCATTGG | 226747 |
rs244455016 | snp | C/T | | | missense | Ahctf1 | Mm_Celera | 1:179752940 | TCCATATTCTGAGTA[C/T]CTTCTAAATTGGCAT | 226747 |
rs244506921 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179772094 | ACCCCCAGCTGTGAC[A/G]ATTCTCTGCAAATAT | 226747 |
rs244550025 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179783655 | TTGTTTGTAATCACA[A/C]CTTTTTTTAAAAAAA | 226747 |
rs244567918 | snp | G/T | | | missense, downstream-variant-500B | Ahctf1 | Mm_Celera | 1:179753487 | CAGTCTCTGCATGTG[G/T]TTCCTTAACAGTCTT | 226747 |
rs244607089 | in-del | -/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179782209 | ACAGCAACAATGGCT[-/G]ATCTACAGCCTGGTG | 226747 |
rs244631531 | snp | C/T | | | downstream-variant-500B, intron-variant | Ahctf1, Gm1305 | Mm_Celera | 1:179744856 | CACATCTCTATTTAG[C/T]AAACTGCACTGGTTA | 226747 |
rs244638407 | in-del | -/AA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179797435 | AGACGACAGAACTAT[-/AA]AAAGGTAGATGAAAG | 226747 |
rs244702818 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179799957 | AAGAATATTTGTTGC[G/T]TTTGGGGAGGACACA | 226747 |
rs244971202 | in-del | -/AG | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750509 | CCCTGGCTCTTCCCA[-/AG]AGAAGAGCATTAGCA | 226747 |
rs245053125 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179790462 | TTCAAATTAAAACTT[C/T]ATTTTTGGAAAAAAA | 226747 |
rs245105773 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179777450 | TTAGATATTTGAGTC[C/T]TATCGCTAGAATTTT | 226747 |
rs245230647 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179774159 | TTAAAATCTATCCTC[C/G]TCCAAAGATTATCCT | 226747 |
rs245237718 | in-del | -/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179794510 | TTTGAATAAGAATGG[-/C]CCCACACATTTCAAT | 226747 |
rs245320140 | in-del | -/ACT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179763123 | AATGAATAATTTGTC[-/ACT]ACTGATTAAAACAAA | 226747 |
rs245332099 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179799696 | CCCCTTTTCTACATT[A/T]CATTCCTTTTCCTTT | 226747 |
rs245333094 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179773377 | CTCATCAAATAGAAC[A/G]GGAAAAGGTCACTGA | 226747 |
rs245365933 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179763182 | ATGATCAAGTGGGTA[G/T]ATTTCTATTAATATT | 226747 |
rs245380053 | in-del | -/AAGT | | | intron-variant | Ahctf1 | Mm_Celera | 1:179778839 | TGAGAAAAATATAAA[-/AAGT]AAAGAAAAGGAAAAA | 226747 |
rs245390583 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179786462 | GACTGAAGGTTTGTG[A/C]CACCACTGCCCAGCA | 226747 |
rs245401366 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179763991 | GTGGTTAAGAGCACC[A/G]ACAGCTCTTCCAGAG | 226747 |
rs245457417 | snp | C/T | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805825 | ATCCTTTGGAACAAA[C/T]TTCCTTCCATATCAG | 226747 |
rs245481524 | in-del | -/AGG | | | intron-variant | Ahctf1 | Mm_Celera | 1:179749352 | AAGCTGAAAAATAGT[-/AGG]AGGTTATAGATAACA | 226747 |
rs245572882 | snp | C/T | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179804570 | TTTACAACCCCCAGG[C/T]CTCAAGAAGAGACTG | 226747 |
rs245617207 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792731 | TACAAGGAGAGAACC[A/T]CCTCCTCCAAGTTGT | 226747 |
rs245725924 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179759795 | CAGACAGCTGTGAAG[C/T]ATCTCATATATATGG | 226747 |
rs245781869 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179757123 | ATCCAGGAGCTCTGG[A/G]AGAGCAGTCAGCTCT | 226747 |
rs245800292 | in-del | -/TGA | | | intron-variant, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179746839 | CCAACTGTGTCGCGT[-/TGA]TGAAGGAATTTGTAC | 226747 |
rs245820883 | in-del | -/AGTG | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764227 | CATCAGTACAGCTAC[-/AGTG]CGTGTACTCATATTC | 226747 |
rs245839562 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179747114 | TTGTGTGAGAAGTGG[C/T]CTCACCCTTTCTAGC | 226747 |
rs245843243 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179780247 | GACGATACTGATAAT[A/T]TCTCAAGTCTCTAAT | 226747 |
rs245883879 | snp | A/C | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805176 | CAGCCTGGTCTCCAT[A/C]GTCGTTCCAAGGCTA | 226747 |
rs245916373 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179760859 | ACTGCATGCAGTTCC[A/G]GGACAGCCAGTACTA | 226747 |
rs245919969 | snp | A/G | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805684 | AAGTACTCTACCAAC[A/G]GAACTACATCCCCCA | 226747 |
rs245920114 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793188 | ACATTAAAGTTTAAA[A/T]AAATTTTTGCTAAAA | 226747 |
rs245952674 | in-del | -/CAAACAAACAAA | | | upstream-variant-2KB | Ahctf1 | Mm_Celera | 1:179805210 | AGAGAAACCCTATCT[-/CAAACAAACAAA]CAAACAAACAAACAA | 226747 |
rs246011950 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179771112 | ATCTGGGCACCCCAC[C/T]GCTACCCCCAACCCC | 226747 |
rs246218358 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179775897 | CACCAGTTAAAGTGA[A/G]CTTTTCATTACTTCT | 226747 |
rs246312657 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179751112 | CTGGGGAGAAGGAGA[C/G]GTAGCTCTAGTAGCT | 226747 |
rs246314424 | in-del | -/ACAA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750101 | ACCACCACTACTCAC[-/ACAA]AAAAAAAAACCCCAA | 226747 |
rs246322467 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179768826 | AGGACTTTAAAAAAA[A/C]AAACACTTGTTGCCT | 226747 |
rs246341836 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764963 | GTTAAGAGAACCGAC[G/T]GCTCTTCGGGAGGTC | 226747 |
rs246376760 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179766397 | ATGCGTGCGCACGCG[A/C]GCTCTCGGAGGATGA | 226747 |
rs246593873 | snp | A/T | | | synonymous-codon, downstream-variant-500B | Ahctf1 | Mm_Celera | 1:179753338 | CTCAGGAGTTTCTTT[A/T]ATTTTTCTAGTTCTC | 226747 |
rs246606295 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179749635 | GGTCAGGGAAGGATC[C/G]TGGGGGGGGGGCAAT | 226747 |
rs246682627 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764193 | CTCAAATTCCCAGCA[A/G]CCACATGATGACGCA | 226747 |
rs246746953 | in-del | -/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179757610 | TTCTGTCTTGCTCCT[-/G]GCTCCGTCCCCTCTC | 226747 |
rs246764903 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793959 | CCCATGAATCTAAGA[A/G]AACAGTGCAACTCTC | 226747 |
rs246793025 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179798758 | ATAAATTTACTAATA[C/T]GTTTCAGAGCATAGT | 226747 |
rs246835147 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792776 | ATGTACACCATGACA[G/T]ACATGTCCTCTTATA | 226747 |
rs247129406 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179789190 | AAGAGGGCATCAGAT[C/T]CCATTACAGATGGTT | 226747 |
rs247165902 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179745818 | ATTTGTAAAACTACA[A/G]AAAGGCAAAATCACA | 226747 |
rs247182924 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179795000 | AATTCCCAGTACCAA[C/T]ATGATGGCTAACAAC | 226747 |
rs247251598 | in-del | -/TACA | | | intron-variant, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179746897 | GCCTGAGAGTCCTGC[-/TACA]TACACAAAGGCATCT | 226747 |
rs247327645 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179801591 | CGTTAAGCTGACATG[A/C]CTCAAAAGATGAGCA | 226747 |
rs247369175 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179747851 | GGGCAGAGACGACTG[G/T]ACTCAGCATACTAAT | 226747 |
rs247472417 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179788779 | TCTGCTCAATAAACA[A/G]AAAGAGTTTTACCTA | 226747 |
rs247500495 | in-del | -/CCT | | | intron-variant | Ahctf1 | GRCm38.p3 | 1:179784029 | AAAAGTCCCCCATAC[-/CCT]CCCCCCCTACTCCCC | 226747 |
rs247508746 | in-del | -/GCATGCA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179800067 | CTCCACAGGCACCAG[-/GCATGCA]GCATGCAGACAAAAC | 226747 |
rs247531090 | in-del | -/TCCGGC | | | cds-indel | Ahctf1 | Mm_Celera | 1:179753177 | GGCGTACCCTGAGGT[-/TCCGGC]TCCGGCTCCACAGCA | 226747 |
rs247557745 | snp | C/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179764788 | GAGCTGGGCACAGCA[C/G]TGGTTCAAACCCAGG | 226747 |
rs247559717 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179754883 | AAAGATGAATGTGGA[A/T]GAATTTATGAATTAA | 226747 |
rs247599629 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179756267 | AAGATGTCTATGTTT[A/G]GTTTGATTAAATACC | 226747 |
rs247684354 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179791223 | AAAATCAATGTCAGA[G/T]AACACAATGCTGCAC | 226747 |
rs247718450 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179796461 | AGATATAGTGAAATG[A/G]TACACTAGTCAATCT | 226747 |
rs247727162 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179800299 | CCCATCTTGTTAAAT[A/G]TACTCTGAGTTCCAA | 226747 |
rs247750642 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179797977 | CCTAAAGTCCCCCCA[A/G]GAGAAAAGCATGCTA | 226747 |
rs247758746 | in-del | -/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750598 | GGTGGCAAGGCTCCC[-/T]TCCTACTGTTAACAA | 226747 |
rs247760850 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179787612 | GAAGCCATGGACAGA[A/G]AATAAGAAGAGGGAT | 226747 |
rs247760861 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179801223 | AACTATGATTATAGG[C/T]ATGCACCACCGTTCC | 226747 |
rs247863667 | in-del | -/ACACACA | | | intron-variant | Ahctf1 | Mm_Celera | 1:179750111 | CTCACAAAAAAAAAC[-/ACACACA]CCCAAAAAACCAAAA | 226747 |
rs247877348 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179798909 | GGTAATTTAAAAAAG[A/T]ATTTATTTTACTTGA | 226747 |
rs247947403 | in-del | -/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179771614 | TGAGAAGGAACACCA[-/T]TTAAATGAAGCAGTG | 226747 |
rs248004016 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179792652 | GAGAGTGTCAAGATG[A/G]CTCACTTGATAAGAC | 226747 |
rs248048780 | snp | A/C | | | intron-variant | Ahctf1 | Mm_Celera | 1:179779516 | TATAAAAATTGTTTT[A/C]AATAAAAAAGTATAG | 226747 |
rs248050575 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179793191 | TTAAAGTTTAAAAAA[A/T]TTTTTGCTAAAAGTA | 226747 |
rs248077180 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179780593 | AGAACAAAACAATAG[A/T]AATACTGAAGACATC | 226747 |
rs248089779 | in-del | -/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179802289 | GTCTCCCCATAGCAC[-/T]AAACATCACCGCTTG | 226747 |
rs248182176 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179761333 | TTATTGTATGCATTT[A/G]GTTTTACAGACCTAA | 226747 |
rs248244411 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179768618 | TGGGAGAGAACTGCC[C/T]GGGAAAGCCTCTGAT | 226747 |
rs248368158 | snp | G/T | | | utr-variant-3-prime, upstream-variant-2KB | Ahctf1, Gm1305 | Mm_Celera | 1:179745899 | GGTACTGACCAGAGA[G/T]CCGAGGAACAGCATC | 226747 |
rs248461581 | snp | G/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179776588 | ATCAAGATATGAAAC[G/T]TGCTCTTTTCTGAAG | 226747 |
rs248464099 | snp | C/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179758895 | TGATTGTTGCAAATG[C/T]CCATCAAACCTACGA | 226747 |
rs248489305 | snp | A/G | | | intron-variant | Ahctf1 | Mm_Celera | 1:179759969 | ATTATTGGCAGTTTT[A/G]AGATGCCCAATGTAG | 226747 |
rs248498685 | snp | A/T | | | intron-variant | Ahctf1 | Mm_Celera | 1:179766159 | AGTATATTAATGTAC[A/T]AAAACTGTCAGCATT | 226747 |