SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3701810 | snp | A/T | 0.396694 | 0.202437 | utr-variant-3-prime | Kat2b | Mm_Celera | 17:53671659 | GGTGTTAGCTTGAAA[A/T]TATTTGAGGTTGAGT | 18519 |
rs3721647 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53590438 | GAGGCTTGACTCTAC[C/G]CATCCCATTGCCCTG | 18519 |
rs6225978 | snp | A/C | 0.5 | 0 | intron-variant | Kat2b | Mm_Celera | 17:53627267 | tttcgttcattactt[A/C]cctcccttcttccct | 18519 |
rs6226577 | snp | G/T | 0.5 | 0 | intron-variant | Kat2b | Mm_Celera | 17:53627396 | CACAGATGGGATGAG[G/T]TGGGTGGGNGAGTGA | 18519 |
rs6226595 | snp | G/T | 0.5 | 0 | intron-variant | Kat2b | Mm_Celera | 17:53627405 | GATGAGNTGGGTGGG[G/T]GAGTGAGTCACACAG | 18519 |
rs6227102 | snp | A/G | 0.5 | 0 | intron-variant | Kat2b | Mm_Celera | 17:53627462 | GCAGCTTGTGGACAT[A/G]GCTGTGGGGCTGGAG | 18519 |
rs6227634 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Kat2b | Mm_Celera | 17:53627563 | GAAAACAAGGGCTGC[A/G]TAACTTTAGCTGGTG | 18519 |
rs6283323 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53594450 | CTCAGCTGCTCCTGC[C/T]GGTCTCCACCTCAAG | 18519 |
rs13461575 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon, nc-transcript-variant | Kat2b | Mm_Celera | 17:53660115 | TTTGATGGGATGTGA[A/G]CTGAACCCTCAGATC | 18519 |
rs29498895 | snp | A/T | 0.375 | 0.216506 | intron-variant | Kat2b | Mm_Celera | 17:53589278 | CCAGTAGCGAGTTTT[A/T]AAAATCCTCTTAGTG | 18519 |
rs29518114 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53621880 | TGGCAGTCTATCGGG[A/G]GCCTCTAGCATCCCT | 18519 |
rs29519210 | snp | A/T | 0.5 | 0 | intron-variant | Kat2b | Mm_Celera | 17:53612501 | GAGATGTCTTAGCTT[A/T]TAGTATGCCAAGATT | 18519 |
rs29533099 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53592826 | GTTGTGAGCCACCAT[G/T]TGGTTGTGGGATTTG | 18519 |
rs29535114 | snp | C/G | 0.401235 | 0.199068 | intron-variant | Kat2b | Mm_Celera | 17:53661589 | GCTCTTCAGTCTTAA[C/G]AAGCAGGTCTAGACT | 18519 |
rs29537198 | snp | A/C | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53588862 | CCTTGGTAGTTAAGC[A/C]AGATTAAAAGACAAA | 18519 |
rs33106248 | snp | G/T | 0.375 | 0.216506 | intron-variant | Kat2b | Mm_Celera | 17:53591562 | CTACATACCCGACCC[G/T]GTCTATCAAAAGGAA | 18519 |
rs33123145 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Kat2b | Mm_Celera | 17:53587480 | AAAACCATCGTGAGT[C/T]GTAGAAGACAGCTTT | 18519 |
rs33125515 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53601927 | TTGAATTCTGTTTGG[G/T]GTGTGTGTGTGTGTG | 18519 |
rs33141880 | snp | G/T | 0.375 | 0.216506 | intron-variant | Kat2b | Mm_Celera | 17:53639334 | TTTGTTTTTGTTTTT[G/T]TTTTTTTTTTTTGTA | 18519 |
rs33149224 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Kat2b | Mm_Celera | 17:53620614 | GTGCAATAGAGCACC[A/G]GCAGTCATTACTGTT | 18519 |
rs33155363 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53614147 | AAATTTATTAATTTG[C/T]CAGGGTTCTAGAAAA | 18519 |
rs33157033 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Kat2b | Mm_Celera | 17:53611195 | TGGGGGCACAGAAGG[C/T]TAAAGTTGAAATAGG | 18519 |
rs33167582 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kat2b | Mm_Celera | 17:53592682 | ACGGGGAGAGGCGTT[A/G]TGAGTTCTTGTTTTT | 18519 |
rs33176456 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Kat2b | Mm_Celera | 17:53601353 | GGATGAAAGGTTTGG[A/G]TTCTTGAATTCTCTT | 18519 |
rs33214150 | snp | G/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53666852 | GATCACCGGGCAGAC[G/T]AGGCTGGCCTCGAAC | 18519 |
rs33255234 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53661451 | TGTTAGAGAATCAAA[A/G]TACTTTTGCTGCACG | 18519 |
rs33272518 | snp | A/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53588267 | AAGGCCACAGAAGGA[A/G]TTTAAGGCCAGCCTG | 18519 |
rs33283996 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kat2b | Mm_Celera | 17:53620301 | CCAGAAGAAGGTGTC[A/G]GAACACAACTCCACT | 18519 |
rs33316568 | snp | G/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53667799 | GTGTGTATGTGTGTG[G/T]GGGGGAATGCACGTG | 18519 |
rs33341708 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53610480 | TAGGGAAACACGATT[G/T]ATATCAAGTATTGTA | 18519 |
rs33370621 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53661469 | CTTTTGCTGCACGGT[C/T]AAAGATGTCTGCCTA | 18519 |
rs33385717 | snp | A/G | 0.5 | 0 | intron-variant | Kat2b | Mm_Celera | 17:53589033 | TCCCAAGTGCTGGGA[A/G]TAAAGGCGTGCGGCA | 18519 |
rs33435892 | snp | A/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53661819 | TTTCAGATGGCTAAC[A/G]TTTTTTCACTTTTTA | 18519 |
rs33448822 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Kat2b | Mm_Celera | 17:53621609 | ACAATATTAGGGCAC[A/T]TTTTTCTTAGGTCGT | 18519 |
rs33451147 | snp | C/T | 0.18 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53667321 | ATAGAATTTGGGCTT[C/T]ACCTATGCTGGGGGT | 18519 |
rs33469840 | snp | C/T | 0.5 | 0 | intron-variant | Kat2b | Mm_Celera | 17:53592879 | GTCAGTGCTCTTAAC[C/T]GTCGAATCATCTCAC | 18519 |
rs33498950 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53661465 | AATACTTTTGCTGCA[C/T]GGTTAAAGATGTCTG | 18519 |
rs33520239 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kat2b | Mm_Celera | 17:53667721 | GTTATTTTTTTGCTT[C/T]AAACCTGTTATCACC | 18519 |
rs33529009 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53601770 | CTGGAGTAGGCTGGT[A/G]ACTCGAAAGATCTAA | 18519 |
rs33530707 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kat2b | Mm_Celera | 17:53669819 | CCCACAGAGGTATTA[A/G]GAATCGAACTCAGGT | 18519 |
rs33552302 | snp | C/T | 0.5 | 0 | intron-variant | Kat2b | Mm_Celera | 17:53598697 | GATGGCTGCCCCTGC[C/T]CCCACTTCTAAAGCC | 18519 |
rs33587077 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kat2b | GRCm38.p3 | 17:53586692 | AGTAAGTTGTCTTTA[C/T]TTTTTTGTTTAGGAG | 18519 |
rs33603458 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53670022 | GGGGTTCTATGTCCT[C/T]TTCTGACCTCAGAGA | 18519 |
rs33629846 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Kat2b | Mm_Celera | 17:53621653 | TCCTTGAGGTCCGTC[C/G]GAAGCCTTCCAGGGA | 18519 |
rs33655889 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53600702 | ATGGGCTCAGCACTC[C/T]ATTACAGTGGCTTAA | 18519 |
rs33706820 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53661426 | TAGAAGAGCAAAACG[A/T]ATTTTGTTTTGTTAG | 18519 |
rs33719275 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Kat2b | Mm_Celera | 17:53662994 | CCGTGGAGTGTGATT[C/T]TTACATCTTAGTCCA | 18519 |
rs45651634 | snp | A/C | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53616902 | TTTTCCTGAAGGCTG[A/C]CTCCCCAGCTTCAGA | 18519 |
rs45686152 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53668970 | GATGACTAGAAGAAG[A/G]AAGACGTTATCCTTT | 18519 |
rs45699721 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Kat2b | Mm_Celera | 17:53619004 | TCTGTGCTGCTTCCA[A/G]ATTGCTTAGACACTT | 18519 |
rs45707337 | snp | A/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53636621 | ACATCTGTAGACTGG[A/G]AATCCAAGGGACGGT | 18519 |
rs45714062 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53659473 | AGACTGTGTATGCAT[A/G]TACGTGTGTGTGTGT | 18519 |
rs45765619 | snp | A/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53650216 | TGTGTAATAGTTTAG[A/G]TCAATGCAGGTAAAA | 18519 |
rs45767908 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53644586 | GAGCCACCTAACATT[C/T]TCTCCTTTTTTTTTT | 18519 |
rs45768076 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53637904 | CTGGGATTATTGGAC[A/C]TTGCTCCTGCCTATA | 18519 |
rs45819707 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Kat2b | Mm_Celera | 17:53614060 | CTGGGAATCCACCAT[C/T]ACTCCATTGCTTTCT | 18519 |
rs45864494 | snp | C/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53638721 | AGCTGTTGGCCTTTG[C/G]TGGGACAGTCTCTCA | 18519 |
rs45870461 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53641155 | TGAGGAATATTTATA[A/C]ATTTTAGAAGCTCAT | 18519 |
rs45879046 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Kat2b | Mm_Celera | 17:53634792 | ATGAAGGTAGATGCA[C/T]TCACCTCAGCGTCCT | 18519 |
rs45881799 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53634921 | CAGAACACTATTAAC[A/G]TAAAAATGAGGCAAG | 18519 |
rs45934912 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Kat2b | Mm_Celera | 17:53659256 | CTGCAAACTCCTGTA[A/C]GCTACCATTCTCTGT | 18519 |
rs45948016 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53588745 | AACTCAGGCCAGTGA[A/C]ACCCTTCTCTATCAT | 18519 |
rs45949155 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Kat2b | Mm_Celera | 17:53634833 | CTTTGATGAAAGGAA[A/G]CAGGGAGAAGAACCC | 18519 |
rs45967650 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Kat2b | Mm_Celera | 17:53612545 | GAGTTGATAGACCGG[A/G]TGCCCTTCACATTGA | 18519 |
rs45978103 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53650949 | CTTCCCAAAAGAGGC[A/G]CTAAGAATATAAATA | 18519 |
rs45995839 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53620478 | CAGACCATTAGTACC[G/T]GATTTCTTTTAAGGC | 18519 |
rs46004958 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53616861 | AGAGCAGGAAACTTG[C/G]TTTATTGTCCTTCTG | 18519 |
rs46010253 | snp | A/C/T | 0.277778 | 0.248452 | intron-variant | Kat2b | GRCm38.p3 | 17:53656648 | GATTGCTTATATACA[A/C/T]GTGTGAGGAGTGGAC | 18519 |
rs46034770 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53591900 | GCCGGGCGTGGTGGC[A/G]CACACTTTTAATCCC | 18519 |
rs46048329 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53612083 | AAGAGTGGCATTTTG[G/T]CATTGTCTTTGCCGG | 18519 |
rs46070909 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Kat2b | Mm_Celera | 17:53661573 | GTCACCTTCCCTCAC[C/T]GCTCTTCAGTCTTAA | 18519 |
rs46087912 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Kat2b | Mm_Celera | 17:53616759 | GATTGAAAGTCTACG[A/C]TATCGTAACCAGCCA | 18519 |
rs46096512 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Kat2b | Mm_Celera | 17:53650163 | TCTTTGTTGAGGAAC[C/T]TTGTTAGCAAATTAT | 18519 |
rs46097692 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53579027 | ATGTATTTCAATGGC[C/T]CTGCACTCCTGACCT | 18519 |
rs46099119 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53639681 | TGGCCTCCAGTTGCT[A/G]TTGAGATGCGGTTGG | 18519 |
rs46126162 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53639038 | GGACAAGCATTTACA[C/T]ATAGAAAACCTGGTG | 18519 |
rs46164956 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53648140 | TCCCTTCTCTTCCAC[A/C]ACCACTTTTTTCCCT | 18519 |
rs46177222 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Kat2b | Mm_Celera | 17:53601293 | GTTTTGTCTGCACAT[A/G]TGGATGTACAAGAAG | 18519 |
rs46179319 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53653622 | TATACTCTGTAAACC[C/T]TGGGAAAACCATTGG | 18519 |
rs46194085 | snp | G/T | 0.5 | 0 | intron-variant | Kat2b | Mm_Celera | 17:53617062 | TAACAATGTCAGAAC[G/T]TATAGAGAAAATAAA | 18519 |
rs46195830 | snp | A/C | 0.375 | 0.216506 | intron-variant | Kat2b | Mm_Celera | 17:53580433 | AATCCTTCTGCCTCT[A/C]TCTCCTGCCAACCCT | 18519 |
rs46209702 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53666130 | CAGTTCTGGATTACA[A/C]ACTGGCTCTTTGGAT | 18519 |
rs46240282 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53638923 | AAAAGCCATACTCTA[A/T]TCTGAACCAAGCAGC | 18519 |
rs46289516 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53655443 | TGCTTTTGGCATTCA[A/G]CAGACCTTCCTAAAG | 18519 |
rs46289545 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53650194 | GCATAATATCTCAGT[G/T]TGGATCTGTGTAATA | 18519 |
rs46301065 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53651084 | TGTGTGAGTGACTCA[C/T]TCATGCATCGAGGCT | 18519 |
rs46323649 | snp | A/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53638130 | GAGGCCAACAGGTCT[A/G]CCAGCTGCTCTTATC | 18519 |
rs46330837 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53587458 | CACATTTAAAGTCAC[G/T]TCAGAGAAAACCATC | 18519 |
rs46347511 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53653460 | CATAGAAATCCTAGG[A/G]TGTCTTACTTCATAG | 18519 |
rs46356087 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53638934 | TCTAATCTGAACCAA[G/T]CAGCATCAAGACAAT | 18519 |
rs46371029 | snp | C/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53665955 | TAGAACTGGGTGGTG[C/G]TGTGGGAGACCAGTG | 18519 |
rs46375125 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kat2b | Mm_Celera | 17:53618701 | ATCCGCCTTTTGCCC[A/G]TTAATGTGTTAACAG | 18519 |
rs46378342 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53660545 | AATCTCTTCACTTTC[A/G]TCGCCAAAAGGATCT | 18519 |
rs46384265 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53586181 | GTTCTCTTCGCTCAC[A/G]GCTGGCTTTTCTTTC | 18519 |
rs46404654 | snp | A/C | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53642726 | ATCACCTAAATTGCC[A/C]TGTCTGCACACCCGT | 18519 |
rs46433042 | snp | A/T | 0.124444 | 0.216185 | upstream-variant-2KB | Kat2b | Mm_Celera | 17:53565058 | TTTTGACCTCTTAAC[A/T]CAAAAGGTGTATCTT | 18519 |
rs46435112 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53642460 | GATGAAAGGTCTCTG[A/G]AAAATCTCTTCCTGC | 18519 |
rs46440441 | snp | A/G | 0.5 | 0 | intron-variant | Kat2b | Mm_Celera | 17:53623780 | CTCTGGATTTATTCA[A/G]TTAAGAAGATTACAG | 18519 |
rs46466085 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kat2b | Mm_Celera | 17:53654622 | GCTTCTTGCTGCTGC[A/G]GAGGAGCATGGGAGT | 18519 |
rs46469563 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53587175 | GACTGTTTCAGTGGT[A/G]GATGGTGGCAGCACT | 18519 |
rs46512665 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kat2b | Mm_Celera | 17:53640091 | GCATCTCACCAAGTA[C/T]ACATCATCTGCTTAG | 18519 |
rs46518539 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53616473 | TTTCAGTGCAAATGA[C/T]AGTCCTTTGTTATTT | 18519 |
rs46533218 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53668999 | TTTATAAGAGCAAGT[A/G]TGGAAGGAGGGATGA | 18519 |
rs46538099 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53638623 | AAGCCTGCTTAAGTA[A/C]CAAAATCATGAACAT | 18519 |
rs46538855 | snp | A/G/T | 0.32 | 0.24 | intron-variant | Kat2b | GRCm38.p3 | 17:53636839 | CTTCTTACTTCCTGC[A/G/T]CCTGACTGGGGTTTG | 18519 |
rs46548896 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53634748 | CTGTTCATTTCTAGA[C/T]CAAGAGACTCTGTTT | 18519 |
rs46551186 | snp | A/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53595603 | ACTTCCGACTTTTAT[A/T]TTTTTTTTTAATGTT | 18519 |
rs46570996 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53670644 | GAGAGGGAGGAGTCA[A/G]CAGTCGCTAATGTTG | 18519 |
rs46571412 | snp | C/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53617362 | TCTGTGAGTACAGTG[C/T]TTAAAACTGAACTGG | 18519 |
rs46572776 | snp | C/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53621713 | AAATTTTAATGTCGT[C/T]AGTTAATTGCAGAAA | 18519 |
rs46596963 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53638998 | TGAGAGCTGCCTGAC[C/T]TTCATCTTTTGGGCA | 18519 |
rs46619234 | snp | G/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53652951 | CAGAACATGGAAAGA[G/T]TTCATATTATCCAGT | 18519 |
rs46645079 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Kat2b | Mm_Celera | 17:53639700 | AGATGCGGTTGGTTG[A/C]CTTAGTGTGTTGTGA | 18519 |
rs46658591 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53654293 | TGAAGTAGGCTTGCC[A/C]TGTAGAGTCCAGGGA | 18519 |
rs46664252 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Kat2b | Mm_Celera | 17:53672792 | CACCTGGTATGAGCA[C/T]CCATTGCTCTTAGTC | 18519 |
rs46695049 | snp | C/G/T | 0.32 | 0.24 | intron-variant | Kat2b | GRCm38.p3 | 17:53633141 | TTTACAACATCTACA[C/G/T]GAGCCAAGACACATG | 18519 |
rs46698644 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53594664 | CGTTGGTGCCCAGAA[A/G]GGCCAGACGAGAGCA | 18519 |
rs46703409 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53612713 | TCAAGCTGATAATTG[C/T]ATGGTTCTATACGTG | 18519 |
rs46709354 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53639732 | GTCCATACAGCAGAT[C/T]CCCACTGGTCTCAGT | 18519 |
rs46710640 | snp | C/T | 0.142012 | 0.225474 | upstream-variant-2KB | Kat2b | Mm_Celera | 17:53565155 | CCTCGGGGCATTCTC[C/T]ACTTTTCTCTGAAGG | 18519 |
rs46717807 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53619166 | TACAGAGCTATGGGT[C/T]TGCTGTACTATGGGT | 18519 |
rs46721094 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Kat2b | Mm_Celera | 17:53649521 | CTGGAAATCGCTTTT[A/C]TGGGCTGTGTTAATT | 18519 |
rs46722451 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53582761 | TCCATTCCGTGGATC[C/T]TGCACAGGCTGTAAG | 18519 |
rs46786224 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Kat2b | Mm_Celera | 17:53613300 | TACTGAGTTCAATTG[A/G]TGTTGCTTGTTGGAA | 18519 |
rs46790325 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53640278 | GTGAAGGTTGCTACA[C/G]GTGACTGATGCTCTG | 18519 |
rs46801839 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53579297 | TATCTGGTCAGGAGG[C/T]GAGAGCTGAAAATTC | 18519 |
rs46803357 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53639800 | TGCTTGTTCCATCCC[A/T]CTGCACTTTGCATGT | 18519 |
rs46840721 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53639054 | ATAGAAAACCTGGTG[A/G]TGGACCATAGAAATG | 18519 |
rs46851625 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Kat2b | Mm_Celera | 17:53652187 | GCCACCAGATCCACT[C/T]GAAATCCTAGGCTCT | 18519 |
rs46900190 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53616455 | ATCAGCTTCAATTGA[C/T]GTTTTCAGTGCAAAT | 18519 |
rs46901232 | snp | C/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53666083 | TTTTTAGTACACTAG[C/T]TGTGGAGTGGAGGTA | 18519 |
rs46906260 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53639105 | GTTGTGATCAAATGT[G/T]TGTACCCAGCCATTA | 18519 |
rs46949395 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53658258 | TGTCGCTGCTGACTT[A/T]TATGGGACAGAGCAC | 18519 |
rs46954349 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Kat2b | Mm_Celera | 17:53635427 | CAAGCTAGCACTGCT[C/T]AGATACAGATGTGAA | 18519 |
rs46996797 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53593597 | AGTTGTGTGCTCCCC[A/C]CCCCCTTATTTCTTA | 18519 |
rs47005422 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Kat2b | Mm_Celera | 17:53618624 | TCATGGGCGCGCTGA[C/T]TCTTAGGTCTACTTT | 18519 |
rs47007398 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53647229 | GCATATGAACACCTG[C/T]TGTATAATGTGTAGA | 18519 |
rs47014364 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53612439 | TGTTTCAGGCTAAAG[A/G]CTGTCATAGTTTTAA | 18519 |
rs47024336 | snp | C/G | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53582693 | AGAGATTTCATCTTT[C/G]TAGGTACTCTGCTCT | 18519 |
rs47071510 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53653563 | CAAAGTTGTGTTGGA[G/T]CTTCAGGAGAAGTAC | 18519 |
rs47134467 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53652020 | TAAAGATAACTTTTG[C/T]GTTGATACATATGTT | 18519 |
rs47149831 | snp | G/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53571823 | GGAGCTGAGGGGGAT[G/T]GCAACCGCATAGGAA | 18519 |
rs47149986 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53620562 | GAGAGGACAGTATCT[G/T]TGGAACGTAATGGCC | 18519 |
rs47154810 | snp | A/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53659432 | TTCAAGAAGCAGGTC[A/G]GTTCCCAACGAAGCC | 18519 |
rs47164200 | snp | C/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53621782 | TGCCGATCATTCTCC[C/T]GTGTAAGCCTCTTGT | 18519 |
rs47184075 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Kat2b | Mm_Celera | 17:53628016 | GAGCCATGGTGCCCA[A/G]TTTCCAGCTCTATCC | 18519 |
rs47201776 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53655290 | GGCACGGGTCCTCTG[C/T]TCCTTTGGCGCTAAG | 18519 |
rs47240057 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53644447 | GTTCAGTGAGTTATA[A/C]TCCATGACTGTCTAG | 18519 |
rs47260008 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53643147 | GTGAACCACTATTCA[C/G]TGAGAAATGTCAGTG | 18519 |
rs47282059 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Kat2b | Mm_Celera | 17:53628912 | ATTGAGAGGTTGTTT[A/G]GCTCTGTTTAAACGC | 18519 |
rs47284753 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53654286 | GCTTTGATGAAGTAG[A/G]CTTGCCCTGTAGAGT | 18519 |
rs47305450 | snp | A/G | 0.5 | 0 | intron-variant | Kat2b | Mm_Celera | 17:53632389 | CCCATGGTAGTAGTG[A/G]TTCTTTTTAAGCAAA | 18519 |
rs47373544 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Kat2b | Mm_Celera | 17:53601609 | CAAGCCCAACCTGGT[C/G]CTTCAGCTCCCTTTT | 18519 |
rs47384005 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53614665 | TGGAAGCAGGATAAT[C/T]TGTTCAGATACGAAG | 18519 |
rs47391032 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53634555 | GTCAAGACTAATGGA[C/T]AGTTGAACGAGAGTG | 18519 |
rs47391855 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53615700 | AAAGCAAGAGATACA[C/T]GAGGCGAGCAAGTGC | 18519 |
rs47392823 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Kat2b | Mm_Celera | 17:53656702 | GAGCAAGTGGTTGCT[G/T]TTGCTACAACCGGCC | 18519 |
rs47408879 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Kat2b | Mm_Celera | 17:53655379 | TCTCTACACTCTGTC[A/G]TATTCTACTCTGTTT | 18519 |
rs47427223 | snp | A/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53650544 | GTATTGGCTTTAGGG[A/G]TTTCGTAACTTCATA | 18519 |
rs47441203 | snp | A/G | | | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53582910 | GAGGGTAAGGAATGG[A/G]GAGTTTAATTTGGAG | 18519 |
rs47481252 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53660688 | CCTGACTCACCTACT[C/T]GGATTTAATTATTTA | 18519 |
rs47487934 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Kat2b | Mm_Celera | 17:53672861 | CACAGTTGTAGGAAA[C/T]TTTATAAACAAAAGA | 18519 |
rs47504007 | snp | G/T | 0.231111 | 0.249285 | downstream-variant-500B | Kat2b | Mm_Celera | 17:53672825 | TACTTCTTAAGCTTT[G/T]GTGAACATGTCTAGA | 18519 |
rs47509453 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Kat2b | Mm_Celera | 17:53658955 | GCTAATGAGATCAGC[A/G]CCATTCATCTGCCTC | 18519 |
rs47538101 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53621944 | CAATCGGACTCCTAA[A/G]ACAATGTGTCAATCG | 18519 |
rs47557573 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Kat2b | Mm_Celera | 17:53659819 | CACTTTTACTTTTAA[A/G]TTTGCTTCCTGTTGG | 18519 |
rs47563330 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Kat2b | Mm_Celera | 17:53673160 | CTTTCGTTCACATAA[A/G]TGATGTCAGAAGTTT | 18519 |
rs47568973 | snp | A/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53642480 | TCTCTTCCTGCGTGT[A/G]AAAACTCATTGTGAC | 18519 |
rs47620199 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53582203 | ACTGCATCTTATCTC[C/T]GTGGTGGGATCTTGA | 18519 |
rs47622886 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53591905 | GCGTGGTGGCACACA[C/T]TTTTAATCCCAGCAC | 18519 |
rs47627703 | snp | A/C | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53642863 | AGAACCCTGTATGCT[A/C]GGAGCCTGTGTGCCA | 18519 |
rs47656217 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Kat2b | Mm_Celera | 17:53640161 | GGAGATGTTTATAGA[A/G]ACACAATCTGTACTT | 18519 |
rs47661920 | snp | A/T | 0.165289 | 0.235211 | synonymous-codon, nc-transcript-variant | Kat2b | Mm_Celera | 17:53624413 | CAGACTCCTGGGAAT[A/T]GTGTTGGATGTGGAG | 18519 |
rs47662713 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53668274 | TAAAACATTCAACTA[C/T]GATCTGTAAGAGTGG | 18519 |
rs47691647 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53579299 | TCTGGTCAGGAGGCG[A/T]GAGCTGAAAATTCTG | 18519 |
rs47695581 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53611956 | CTGCTCTTTTTACAC[C/T]TTTCTGCCCATGCCA | 18519 |
rs47704023 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53577053 | AGGCCTCTATAGATG[A/G]CTTCTACCTTTCTTA | 18519 |
rs47705392 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Kat2b | Mm_Celera | 17:53658064 | ATACTGAAGTTCCGT[C/T]TATAATTGTGTTTTC | 18519 |
rs47729029 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53614181 | TTTTGTGAGATTACA[C/T]CATCTTCCTCCTTCA | 18519 |
rs47730660 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53638651 | CATCCGAGTATATCA[A/G]TGCTTTCACGGACTC | 18519 |
rs47733789 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53655370 | AAGAGCACTTCTCTA[C/G]ACTCTGTCGTATTCT | 18519 |
rs47740234 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53643446 | TGTGTGTTGAGGCAG[A/C]GGACACACACACTCA | 18519 |
rs47741855 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53670356 | GCATCCATGAGTCCT[C/T]CACTGTCTCTTAGCC | 18519 |
rs47746742 | snp | A/G | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant | Kat2b | Mm_Celera | 17:53632554 | TGTGAACAACTTCGT[A/G]CAGTACAAGTTTAGT | 18519 |
rs47766857 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53638174 | TTGCTAGTAATCTTG[C/T]TGGTTGATCTTGCTG | 18519 |
rs47798880 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53616591 | TGCTTCAGCTCCTAC[G/T]ACTGAAAAGACAGAC | 18519 |
rs47811202 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53578592 | AGAATTTGATTCTGG[C/G]ACCCACCAAAAGGGC | 18519 |
rs47811428 | snp | C/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53632833 | GACAGCATGCCTATG[C/T]AGTTTAGTTTCAAGT | 18519 |
rs47811904 | snp | G/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53641604 | CTCTGTCAGGAGATA[G/T]TGACCTTTTGAAGAT | 18519 |
rs47821260 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53616282 | GGTCTCTGGGATACC[C/T]AGGAATCCGAGGTCT | 18519 |
rs47822009 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kat2b | Mm_Celera | 17:53625241 | CCTAGAATCTAGGTG[C/T]CACGAGTGTGAGGTG | 18519 |
rs47840894 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53650571 | CATACATGAGCCAGA[C/G]CTTGGCCTGCTCAGA | 18519 |
rs47850143 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53660602 | CTCTGGCTCACAATA[C/T]CCTGTCACTCAGGTA | 18519 |
rs47866036 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53638789 | CCAGTCTCTTCCCAT[A/G]CTTCTCACTTCCTAC | 18519 |
rs47897548 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53585494 | GCACTCAAAAAATAG[C/T]TGTCGAGTAAGATGA | 18519 |
rs47917365 | snp | A/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53636657 | AATCTTTTCATTTTC[A/G]AGCACTAGCGTTGAA | 18519 |
rs47926288 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53612151 | AGCCAGTCCACTGTT[A/G]AGCTGAGTCTGGTGT | 18519 |
rs47940524 | snp | C/T | 0.5 | 0 | intron-variant | Kat2b | GRCm38.p3 | 17:53614588 | TAATCAAGTTGTGAA[C/T]GAGGGACTTCTGTAA | 18519 |
rs47962507 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Kat2b | Mm_Celera | 17:53636339 | CCTACATAGGATCGT[C/T]TGGGGTCAGATACAG | 18519 |
rs47993713 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kat2b | Mm_Celera | 17:53614009 | TCAGAGGCCAGAGAT[A/G]TGATCCTCTTGCTTC | 18519 |
rs48009125 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53621314 | AATGAATGAATGAAT[A/G]AATAATTTGGGGCAT | 18519 |
rs48011057 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Kat2b | Mm_Celera | 17:53634389 | AGCCTTCTCTTTCCT[G/T]ACTCTCAGCTTCTTG | 18519 |
rs48025097 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53588446 | TTTTTGAGATTCAAA[A/C]GTGTGGCTGCATTCA | 18519 |
rs48049996 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53654664 | TCGGCTCAGAGAAGG[C/T]TCAGGATGTGAAGTT | 18519 |
rs48058729 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Kat2b | Mm_Celera | 17:53658474 | GGATACACGGCCGTC[A/G]CCACTATAGTTTTCA | 18519 |
rs48064202 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53661185 | TGTGGGTGACATCTG[C/T]TTCATCCAGTACTCC | 18519 |
rs48065596 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Kat2b | Mm_Celera | 17:53654388 | CCACAAGTGTTTTAC[A/G]TAACCAAACAAGATA | 18519 |
rs48075353 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53666233 | AAGTCACTCTTATTC[G/T]AAGGGTTGTTCAAGA | 18519 |
rs48130405 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Kat2b | Mm_Celera | 17:53584674 | GGTATTCATTTAACT[A/C]TGTGGACCATTTTTT | 18519 |
rs48139519 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53616882 | TGTCCTTCTGCACAG[C/T]ACTTTTTTCCTGAAG | 18519 |
rs48151149 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53666975 | TTTGAAGCTAACAGA[A/G]TGAGGGTAGGTTAAG | 18519 |
rs48167780 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53640009 | GTAAGGGCCTAGTCA[G/T]TACACAGTGACATTG | 18519 |
rs48175227 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53585407 | TTTGAAAACCATTTC[A/T]TGCCCATGTTCTGAG | 18519 |
rs48185052 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Kat2b | Mm_Celera | 17:53655878 | AGTATCATGAGGAAT[C/T]GTCAACAGCATCTGC | 18519 |
rs48205574 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53591888 | AAAATATTTTTGGCC[A/G]GGCGTGGTGGCACAC | 18519 |
rs48235538 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Kat2b | Mm_Celera | 17:53637974 | GTGCTATCTCATTCT[A/C]TAGAGTCCAGTGAAG | 18519 |
rs48239291 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53663442 | TAAAAACTTGTACAG[C/T]CTCAGGAGCACCATC | 18519 |
rs48258444 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Kat2b | Mm_Celera | 17:53649475 | TGTCAGCTTCTTACT[C/G]GCTAGGAGTGAAGGT | 18519 |
rs48298995 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Kat2b | Mm_Celera | 17:53660502 | CGCCACCACGCCAGG[C/T]TCGTATAGTACGAGC | 18519 |
rs48300678 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53653316 | TCAGCCCTTGGAATA[C/T]AGCTGCCTTCTGTCC | 18519 |
rs48327801 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53635013 | CCTGAGATGGCACAT[A/G]TCTATAATCTTAGTC | 18519 |
rs48331247 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53579330 | CTTTGGAGAAACATC[A/G]TATTCAAAAGTCTGA | 18519 |
rs48389046 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Kat2b | Mm_Celera | 17:53617177 | TTGCTTGCAGTTTAC[A/G]CTATATTCAGTTCCT | 18519 |
rs48400089 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kat2b | Mm_Celera | 17:53617147 | TGTTTTTCTGAACTG[C/T]GATTAAAGGTTGCAT | 18519 |
rs48445248 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53661649 | TGATCGCTTGACACT[A/G]GCATTGTGCTGACAG | 18519 |
rs48459412 | snp | A/C | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53621727 | TCAGTTAATTGCAGA[A/C]ATCCTTATTTCCTGG | 18519 |
rs48459521 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Kat2b | Mm_Celera | 17:53614682 | GTTCAGATACGAAGA[A/T]CATTCAATCAAGTGT | 18519 |
rs48533861 | snp | A/G | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant | Kat2b | Mm_Celera | 17:53641199 | TGTGCCTAGGTTTCT[A/G]TCCATGTTGGAAGAA | 18519 |
rs48535983 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53638745 | TCTCTCAGCTAGGTC[A/G]TCTAAATTTATCCTA | 18519 |
rs48547210 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53641451 | ATGAAGAACAAGTAA[A/G]TACTAACTCAAATTC | 18519 |
rs48599284 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Kat2b | Mm_Celera | 17:53634976 | GTCTGAAGCTTTATT[C/T]ATTGAAAAAAGTAAA | 18519 |
rs48617719 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Kat2b | Mm_Celera | 17:53586281 | CTTTCCAGCTTTTGT[C/T]GTTGGTTGTTGCTGA | 18519 |
rs48663562 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53615785 | GACTCCACCAGTGAG[C/T]GATGAGCTGTCAGGA | 18519 |
rs48691965 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53578611 | CACCAAAAGGGCTCA[C/G]TGGTTCCAAGCTCCA | 18519 |
rs48727468 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Kat2b | Mm_Celera | 17:53614259 | GATAGTTTAACAAAC[C/T]GTCTTGGACCCATCA | 18519 |
rs48743152 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Kat2b | Mm_Celera | 17:53655745 | GTAGCGTGTGGAAGC[C/T]GCACACACAATCCAT | 18519 |
rs48771596 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53599272 | ATTAAAATAATTTTT[A/C]GAAATAATGTTATTT | 18519 |
rs48786398 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53576814 | ACATCCATTTCTGTC[C/T]CAGCTGCATGTTTGC | 18519 |
rs48794049 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Kat2b | Mm_Celera | 17:53655294 | CGGGTCCTCTGTTCC[C/T]TTGGCGCTAAGGCTG | 18519 |
rs48797733 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Kat2b | GRCm38.p3 | 17:53656820 | TCTCTTGCAGAGTTT[A/G]ATAGTGTGGGCAGAA | 18519 |
rs48820130 | snp | C/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53637678 | GAATCTGACCTTACA[C/T]GGACAGTGACAGGAT | 18519 |
rs48830584 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53655734 | GTTGTTCAACAGTAG[C/T]GTGTGGAAGCTGCAC | 18519 |
rs48844761 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53656253 | TAGTGGCCCTGAGCT[C/T]CTGATCCTATTGCCT | 18519 |
rs48867231 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53632792 | TACTATTCACTTCTG[C/T]TCTGCTCAGTGACTC | 18519 |
rs48876969 | snp | A/G/T | 0.473373 | 0.11227 | intron-variant | Kat2b | GRCm38.p3 | 17:53643091 | TGTCACCTGGGTTGC[A/G/T]TATTGAATCCCGTGA | 18519 |
rs48877172 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53645298 | GGATGTTGTCCTGTA[C/T]ACATGTTCTTGAGAC | 18519 |
rs48897713 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53667109 | TATTGGTGTGTGTGC[A/G]AATGGTGTGTGCATG | 18519 |
rs48915238 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53591696 | GGAGGAAAGAGTTGG[C/T]ATGAGTATGATCACA | 18519 |
rs48918761 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53649098 | GAACGTTTCCATAGT[A/G]AAGAATTTCAAGCTT | 18519 |
rs48935749 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53639878 | ACTAAGGGCATCAAT[C/T]CCTCACCACACTGTC | 18519 |
rs48939856 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53668142 | TTGCTTGTTTCTACT[A/G]GAGAGGGCTATGAGC | 18519 |
rs48959907 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kat2b | Mm_Celera | 17:53614641 | ATGATGGAGACTCTT[C/T]TACATCTTTGGAAGC | 18519 |
rs48975963 | snp | C/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53642607 | GCTTGTACCCTTAAG[C/T]CAGGCCATTCATTCT | 18519 |
rs48979528 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kat2b | Mm_Celera | 17:53613329 | AATGTTGACAAAGTG[A/G]TCCTTCCCAAAGGCA | 18519 |
rs48984325 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53584278 | GTGTGTAGAACTGGA[A/G]AGCTTGGGAGGATGG | 18519 |
rs49008256 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53650968 | AGAATATAAATATGA[C/G]TGCTGCTCTATTTCA | 18519 |
rs49042067 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53588369 | TGATCCTGGGTTCCA[C/T]ATTTAGTACTGCCAC | 18519 |
rs49052652 | snp | G/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53655151 | AAAGAAGAAGAGTAT[G/T]TACGTGGACTTGGCT | 18519 |
rs49065692 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53635114 | CAAAATAAATGAAAC[A/G]GATTTAACAGAATTG | 18519 |
rs49068593 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Kat2b | Mm_Celera | 17:53660718 | ATCCTGCAGAGACAT[C/T]TCTTCTAGTGTCTAT | 18519 |
rs49078089 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Kat2b | Mm_Celera | 17:53635351 | ATATTCATAAACCAT[A/C]ATTTTTATAGCAGAA | 18519 |
rs49083434 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Kat2b | Mm_Celera | 17:53566143 | CTCTTGGCATTGCAT[C/T]ACTCTGCGTTAAAAG | 18519 |
rs49092309 | snp | A/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53668003 | CTCCTTTTTGTCCTC[A/G]CTGAGCCCTGTTGAA | 18519 |
rs49093323 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53616722 | CTTCTTTCTGGTTTT[C/T]CTGCCTTCTCCCAAA | 18519 |
rs49104370 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53612610 | TAAGGAATCTACCTA[C/T]GACTGGGCTGAGCTG | 18519 |
rs49113926 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53635135 | AACAGAATTGCTTGG[C/T]ACTCTTATGAGTAAA | 18519 |
rs49125916 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53657276 | CTGTTTCTCTGTTGG[A/C]TCACGCAGATCCTGA | 18519 |
rs49126614 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53657425 | ATCTCTCTCGCCCCA[G/T]CAACTTGACACACTC | 18519 |
rs49130167 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Kat2b | Mm_Celera | 17:53648191 | TATTAGAAAATTAGT[A/T]GGGAGACCAGTGTGA | 18519 |
rs49138550 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53645845 | TTTAAGTGAACAACC[C/T]CTCAGGTATTTCTGT | 18519 |
rs49144455 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kat2b | Mm_Celera | 17:53642412 | TTTTGACATACATGC[A/G]CTGTTTGAGGTGACA | 18519 |
rs49174254 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53638204 | GGCTGGTATTGAAGG[C/T]CTCGTTTCTTCCACT | 18519 |
rs49186517 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53636595 | TGTCTCTGGAAGTAG[C/T]AGAGTCCACCACATC | 18519 |
rs49195310 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53662680 | ACTCTCAAATGTCAG[A/G]CTCCACTTGTGGAAA | 18519 |
rs49216480 | snp | C/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53643291 | AGTGAAAAACACCAA[C/T]GCAATTTATTTGGAA | 18519 |
rs49220485 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53636412 | GCCCTTGCTTCACCT[A/T]ACCTGTTAGCGTCCT | 18519 |
rs49221522 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53649321 | TGCCTGTGTCTCATA[G/T]GAAAGCAATTCTCTT | 18519 |
rs49228692 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53618352 | AGGCGCCACCTCCTC[A/G]GGACTCCTCAGCTCT | 18519 |
rs49255145 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kat2b | Mm_Celera | 17:53622387 | CCACAAGGCAAATTT[C/T]GTCACTGATAAGCAA | 18519 |
rs49301872 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53667526 | GTCTTACATGTCTCT[C/T]CATGGCATTCATTTC | 18519 |
rs49304715 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53639901 | ACACTGTCAAGTAAT[A/G]AGAGCTGTGTAATAG | 18519 |
rs49318118 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53652618 | CAAGCCTTTTGAGAC[A/G]GGGCCTCAACCTAGG | 18519 |
rs49332055 | snp | C/G | 0.473373 | 0.11227 | intron-variant | Kat2b | Mm_Celera | 17:53634358 | CACCTTCCTCTATCT[C/G]TGTGAGCTGTAGAGC | 18519 |
rs49357468 | snp | C/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53613261 | CAGATGCATGTCCTA[C/T]TTCCATGTCCTGTCC | 18519 |
rs49385016 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53642363 | TGCTATCATCTTTAG[C/T]AGTGTTAAGTCCATC | 18519 |
rs49385363 | snp | A/C | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53636364 | ATACAGACTGAGGCC[A/C]CCTAGGTGTACAGCA | 18519 |
rs49404374 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Kat2b | Mm_Celera | 17:53638117 | AACAGAATAGGAAGA[C/G]GCCAACAGGTCTACC | 18519 |
rs49408076 | snp | C/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53654075 | CATGTGGATGTTATG[C/T]TCTTTGATGTAACGT | 18519 |
rs49420319 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Kat2b | Mm_Celera | 17:53657321 | CATCCATTGCTCATT[C/T]TTGGTCTTCCTGAAG | 18519 |
rs49446889 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Kat2b | Mm_Celera | 17:53648668 | CATCTCCTCCCCAAG[C/T]ACATTAGATCCATCA | 18519 |
rs49454433 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53633483 | CTTTCCATGATATTC[A/T]TACCATGTATGGACT | 18519 |
rs49464948 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Kat2b | Mm_Celera | 17:53641283 | TTCCAGAACCAGCCC[A/G]CTAGGAATCCAAACA | 18519 |
rs49467847 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53658467 | GATCTCTGGATACAC[A/G]GCCGTCGCCACTATA | 18519 |
rs49479615 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kat2b | Mm_Celera | 17:53615638 | CTAAACAAAACATTT[A/G]TTACTGAAGGCTGTG | 18519 |
rs49489688 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53638946 | CAAGCAGCATCAAGA[C/T]AATACCCATTCATCT | 18519 |
rs49519100 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53620723 | ACTGTGCTGATGAGA[C/T]TTCTCGAGGGGTAGG | 18519 |
rs49524045 | snp | G/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53645462 | GGTGAAGACTGCCTT[G/T]TTCTGGTACCCCAAA | 18519 |
rs49526008 | snp | A/G | 0.375 | 0.216506 | missense, nc-transcript-variant | Kat2b | Mm_Celera | 17:53624396 | TCAGAGGAAGAGATG[A/G]ACAGACTCCTGGGAA | 18519 |
rs49528234 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53618840 | TTTAATCCCAGTGCT[C/T]AGGAGGTATGGGCAG | 18519 |
rs49560626 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53618597 | TTGACCACTGTCATC[A/G]ACCACATCCTCTCAT | 18519 |
rs49578854 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53648982 | CTGGTCACCTGTAAC[C/T]TAGAGGCCACTATAG | 18519 |
rs49589016 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Kat2b | Mm_Celera | 17:53672821 | TCTTTACTTCTTAAG[C/T]TTTTGTGAACATGTC | 18519 |
rs49630344 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Kat2b | Mm_Celera | 17:53643511 | CTGCTATTTCAACAT[C/T]ATTTTTGTTGCTGTG | 18519 |
rs49633751 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53612583 | GGGAAATATGATGCA[C/G]TTAACAGAGCTTAAG | 18519 |
rs49651992 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Kat2b | Mm_Celera | 17:53671346 | AATGAACTGTGTGAT[A/G]TTTGAAGTCTCCTTG | 18519 |
rs49658538 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53638683 | TGTGGTTAAATAAGA[C/T]ACAGAAACTTCTAAT | 18519 |
rs49680145 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53647696 | GTTTTGAATTCACTG[C/T]GTAGTCAAGGAAGAC | 18519 |
rs49687110 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53612325 | ATCTCGCAGGAGAAA[C/T]CAACACACTAATAAG | 18519 |
rs49708609 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53612020 | ACCTGTCTTTAGGCA[A/G]AATGGGATCACCAAG | 18519 |
rs49713228 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53621626 | TTTTCTTAGGTCGTC[G/T]GTGCAGGGTCTTCCT | 18519 |
rs49725527 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53588465 | TGGCTGCATTCACCA[A/G]TAGCCACTTTCTGTT | 18519 |
rs49748403 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53612996 | CAATTAGGTAAGTGC[G/T]ATACTACTGAGTTAC | 18519 |
rs49768926 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Kat2b | Mm_Celera | 17:53649632 | TCTCTTGACTTTTCA[C/G]TGGAAAGTTTGCTGA | 18519 |
rs49804605 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53622197 | GTAAGTTGTTCAGAC[A/G]CATCAGAAGCTTGGA | 18519 |
rs49823253 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53640025 | TACACAGTGACATTG[C/G]TGGTGGTTTCTACGC | 18519 |
rs49839632 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53666108 | GAGGTAGGGATCTTA[C/G]TGTGGACAGTTCTGG | 18519 |
rs49859178 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53642298 | TGAGCGAGAGAAGGC[A/G]ATTCTGCTTTCAGTA | 18519 |
rs49904664 | snp | A/G | 0.5 | 0 | intron-variant | Kat2b | Mm_Celera | 17:53625303 | CCTGTCGTCATGATG[A/G]TGATCACATGATGAT | 18519 |
rs49910294 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53593897 | CCACTTCATTTGTAT[A/C]TTTATAAACTTGGCT | 18519 |
rs49910461 | snp | C/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53670462 | AGAAATCCTTTTCAG[C/T]AGAGTACTCAGGAAT | 18519 |
rs49926065 | snp | C/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53654967 | GTCTATAAAGAGAAA[C/T]GAATATTAAGGAAAT | 18519 |
rs49927336 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53627750 | TTCCAAACGACAGGA[A/G]AGATATATTTGCTTC | 18519 |
rs49928650 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53620381 | GAACTGAACCCAGAT[C/G]CTCTGGAAGAGCAGC | 18519 |
rs49928821 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Kat2b | Mm_Celera | 17:53658770 | TTTTTTTGCTGACTC[A/G]GATTCTGGGTTTCTT | 18519 |
rs49929423 | snp | A/C | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53655397 | TTCTACTCTGTTTTT[A/C]TGAGGACACTGTTTC | 18519 |
rs49939584 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53587625 | CTTCTCACCCTTCCC[A/G]GACTCGAGCTTCATG | 18519 |
rs49944633 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53632980 | CCATGTGATACAGAG[A/G]AATGTTACCCAGTCC | 18519 |
rs49945153 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Kat2b | Mm_Celera | 17:53623479 | GGGAACATAGAGCCT[A/G]GTTCATCTGTAGCAG | 18519 |
rs49954245 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Kat2b | Mm_Celera | 17:53634681 | GTGGAGCTAACCATG[A/T]GAAGAGAAACCTGCC | 18519 |
rs49954973 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53654045 | ATTCCACACATGGGG[G/T]CTTGACAGTTCCTAC | 18519 |
rs49989110 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53645438 | CAAAAGAAATAATCA[C/G]TGTCTTGAGGTGAAG | 18519 |
rs49993514 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53580733 | GTGGCCTGTTTGGAT[G/T]TAGGACAGGTATAGT | 18519 |
rs50049677 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53657204 | CCCCGTGATCAACTC[G/T]GCATAATAAACATGC | 18519 |
rs50059241 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Kat2b | Mm_Celera | 17:53657535 | TGTATAACAGAAATC[C/T]GAGTTTCACATAAAA | 18519 |
rs50085332 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53619117 | GAGAAGTCCAGGTGA[A/G]TGTACTTAGTGGAAC | 18519 |
rs50091873 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53612097 | GTCATTGTCTTTGCC[C/G]GTTTGCTGTTGGTCC | 18519 |
rs50092784 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53591904 | GGCGTGGTGGCACAC[A/G]CTTTTAATCCCAGCA | 18519 |
rs50096514 | snp | C/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53633508 | TGGACTTGTTTGAGA[C/G]AGGGTGCATGTAGCC | 18519 |
rs50116851 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53578510 | TTTGTACCTATTGAG[C/T]CATCTTCCCGGCCTT | 18519 |
rs50141779 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53612951 | ATTTTTTGGTCCTTA[C/G]TGCTAGGAATCTAGC | 18519 |
rs50144181 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53642251 | TGGCTTCTTCACCTG[G/T]GACATCTATTTTCTA | 18519 |
rs50144678 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53661049 | TGGAGAAGGCTCCAG[A/G]TGTGAGTTTACAGTG | 18519 |
rs50154001 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Kat2b | Mm_Celera | 17:53619261 | GCTGGTGTTTGTAAC[G/T]TGACAGAGAAGCGCC | 18519 |
rs50157808 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53618616 | ACATCCTCTCATGGG[C/T]GCGCTGACTCTTAGG | 18519 |
rs50165207 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Kat2b | Mm_Celera | 17:53638430 | GGTGTTTGGGAGAAC[A/G]TTGCTTCGCTCGGTC | 18519 |
rs50199590 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53649477 | TCAGCTTCTTACTCG[C/T]TAGGAGTGAAGGTGT | 18519 |
rs50210050 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB | Kat2b | Mm_Celera | 17:53565299 | TTCTGTTTACCTTTG[A/G]GCAGCTGCCAGAATT | 18519 |
rs50235989 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Kat2b | Mm_Celera | 17:53651686 | AGAGTTGGAAGATCA[C/T]GCTCCGTATTCTATA | 18519 |
rs50269218 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Kat2b | GRCm38.p3 | 17:53607761 | AGCAAAATGTTTGAG[C/T]TGTAGTTACAACCAG | 18519 |
rs50274136 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53652273 | ATCTCCTCAGCTCTT[C/T]TAAAATATTTTCTAC | 18519 |
rs50311424 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kat2b | Mm_Celera | 17:53619151 | GCGAAGGTCACAGCA[C/T]ACAGAGCTATGGGTC | 18519 |
rs50325197 | snp | A/T | 0.5 | 0 | intron-variant | Kat2b | Mm_Celera | 17:53629444 | AGAGGAGCTCTTTTT[A/T]CATGCATTTAAGGCT | 18519 |
rs50352354 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53619042 | GCTTCTGGTGCAAAG[G/T]ATCAGGGACACACTT | 18519 |
rs50374365 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Kat2b | Mm_Celera | 17:53652068 | ACATCGGTGCCCATG[C/T]ATGGCAGATTCTCTC | 18519 |
rs50381685 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kat2b | Mm_Celera | 17:53666067 | AGGGACGTTCTGTGC[A/G]TTTTTAGTACACTAG | 18519 |
rs50390976 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Kat2b | Mm_Celera | 17:53614677 | AATCTGTTCAGATAC[A/G]AAGAACATTCAATCA | 18519 |
rs50397572 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Kat2b | Mm_Celera | 17:53640004 | TGGGTGTAAGGGCCT[A/C]GTCAGTACACAGTGA | 18519 |
rs50411140 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Kat2b | Mm_Celera | 17:53602210 | TCTCTTCCATCCAGA[A/G]TTTCCACCAGTTTGC | 18519 |
rs50441595 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53642405 | CTAGGAGTTTTGACA[C/T]ACATGCGCTGTTTGA | 18519 |
rs50442597 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Kat2b | Mm_Celera | 17:53672409 | ATTAAGTGTCTCAGA[C/T]TGGTTTTAAAACAGC | 18519 |
rs50444012 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53612046 | CCAAGTCCTGTCTTA[C/G]TACTCCACCCACGAC | 18519 |
rs50478574 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Kat2b | Mm_Celera | 17:53579744 | GTTCTTTCTATACTC[A/T]GTGTGTGTGTTGCTT | 18519 |
rs50487860 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53648190 | CTATTAGAAAATTAG[G/T]AGGGAGACCAGTGTG | 18519 |
rs50496654 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53618619 | TCCTCTCATGGGCGC[A/G]CTGACTCTTAGGTCT | 18519 |
rs50523252 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kat2b | Mm_Celera | 17:53613299 | CTACTGAGTTCAATT[A/G]GTGTTGCTTGTTGGA | 18519 |
rs50532725 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Kat2b | Mm_Celera | 17:53618108 | GGAGCAAACCCTACT[C/T]ACGCCCACACTAAAT | 18519 |
rs50579201 | snp | C/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53618036 | GGTTAAAGTAGCCTT[C/T]GTCTATTTCTTTTAC | 18519 |
rs50592779 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53645569 | ATTTCAAAGTTACAT[A/G]CAAATCATGGAACAT | 18519 |
rs50595899 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53617966 | TCCGTTCTTTTTCTA[A/G]CATGGAGTATGTGAC | 18519 |
rs50597950 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Kat2b | Mm_Celera | 17:53580486 | CCGTGAAGTGTATAG[C/T]AGCCATTTGGAAGGT | 18519 |
rs50671185 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53667394 | GTCAGTGTGCTGTGA[A/C]AAGTAGCTGAAGGAA | 18519 |
rs50675944 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53667528 | CTTACATGTCTCTTC[A/G]TGGCATTCATTTCCA | 18519 |
rs50699172 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kat2b | Mm_Celera | 17:53621023 | ACTACATTGTAAGAC[C/T]TGAGAAAATCAATTC | 18519 |
rs50702946 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53663522 | TAACCACATGTTTCC[C/T]TATGCTTTTCAGATC | 18519 |
rs50705612 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, downstream-variant-500B | Kat2b | Mm_Celera | 17:53670881 | TGATTTCTTTCCCTT[A/G]GACACACATCAGCAG | 18519 |
rs50735222 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53650296 | AGGGAGGCTCAAGAC[A/G]TTTCCAGGAAATGAA | 18519 |
rs50742046 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53621934 | CCAGCAAGGTCAATC[A/G]GACTCCTAAAACAAT | 18519 |
rs50742639 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53647636 | CATTCTATTTGAGGC[A/G]ATTAAAACAGTCTTT | 18519 |
rs50745171 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53652328 | CTAATCAGAAGTGAT[A/G]TATATATTTCCTGTC | 18519 |
rs50754441 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Kat2b | Mm_Celera | 17:53655359 | TGCTGGGTACAAAGA[A/G]CACTTCTCTACACTC | 18519 |
rs50756495 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Kat2b | Mm_Celera | 17:53612120 | GTTGGTCCAAATGAC[A/G]TAGCTCCACCTCTGA | 18519 |
rs50772666 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Kat2b | Mm_Celera | 17:53618690 | GTGTTTACATGATCC[A/G]CCTTTTGCCCGTTAA | 18519 |
rs50776047 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53582159 | GTCAGTCAAGATGGC[A/G]TCTGTCTTTCATCCT | 18519 |
rs50787761 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53634673 | CCAAAAAGGTGGAGC[C/T]AACCATGAGAAGAGA | 18519 |
rs50797944 | snp | A/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53651389 | TGAACTTAGGTTCTC[A/G]GGTTTTGTATCAAGC | 18519 |
rs50812521 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53592409 | TCAGGGCAGGAACCT[A/G]GAGGCAGGAGCTGAT | 18519 |
rs50813070 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Kat2b | Mm_Celera | 17:53566096 | TGCAGTTTCACAGCA[A/G]GTGTCACTCCTTTGA | 18519 |
rs50819148 | snp | A/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53615769 | CAGCTGCGGAGGATC[A/G]GACTCCACCAGTGAG | 18519 |
rs50881938 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53629820 | TTCACTTAGACTCCA[C/T]TCTGTATGTAGGAGA | 18519 |
rs50900243 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Kat2b | Mm_Celera | 17:53656686 | GATGGTGGGAGGTCC[C/T]GAGCAAGTGGTTGCT | 18519 |
rs50919874 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53644387 | TCTTCACTGTCTTGT[A/T]TGTTCACTATTTTAT | 18519 |
rs50926116 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53656026 | CCTGGGCAGTGCAGG[A/G]CGAAGGAGTCTATTA | 18519 |
rs50991318 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53649540 | GCTGTGTTAATTGCT[A/C]ACCATTGCGCATAGC | 18519 |
rs51002562 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Kat2b | Mm_Celera | 17:53672438 | GCTTTGTACCGATTT[C/T]GCTGAAGCGTCTGTC | 18519 |
rs51050160 | snp | C/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53666016 | ACAATGAGTGTGTCT[C/T]GAGTGGGATTTGTGA | 18519 |
rs51056258 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53644438 | CATTCCTCTGTTCAG[C/T]GAGTTATACTCCATG | 18519 |
rs51060268 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53645749 | AAAGTTAGTGAGTAC[A/G]GTGTGAAAGTGTGTT | 18519 |
rs51062626 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53633999 | GAAAACAAAGTGAAG[C/T]TGGGTGTGGTGGTGT | 18519 |
rs51098598 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53656115 | AGACGCATTTTCTGT[G/T]CCAAGTGTGGTTAGG | 18519 |
rs51100469 | snp | C/G/T | 0.426035 | 0.177515 | intron-variant | Kat2b | GRCm38.p3 | 17:53655853 | ATATGTTTCATTTAA[C/G/T]GTAAAATTCAGTATC | 18519 |
rs51103376 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53659099 | GTGTTATTTTCAAAG[A/G]ACCCGGAGCTAGTGT | 18519 |
rs51128931 | snp | A/T | 0.231111 | 0.249285 | synonymous-codon, nc-transcript-variant | Kat2b | Mm_Celera | 17:53638523 | TGAGAAACGCACGCT[A/T]ATCCTCACACATTTC | 18519 |
rs51146143 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Kat2b | Mm_Celera | 17:53613372 | CAATTTTCAGTGTAC[C/T]ATGGCCTTCCTTAGG | 18519 |
rs51162689 | snp | C/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53650312 | TTTCCAGGAAATGAA[C/G]ACATGACTTGGGTAG | 18519 |
rs51194148 | snp | C/T | 0.142012 | 0.225474 | upstream-variant-2KB | Kat2b | Mm_Celera | 17:53565320 | TGCCAGAATTTACAG[C/T]TCACTATAATACAAT | 18519 |
rs51204051 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53658453 | TTGTGGTGGTCACTG[A/T]TCTCTGGATACACGG | 18519 |
rs51205193 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53653589 | AGTACAGAGGACAGC[A/T]CCATATCTGCTATGC | 18519 |
rs51215943 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53641504 | GCAGTGCAAGCACAA[A/G]CCAAACAGTTGAAAC | 18519 |
rs51221660 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53644486 | TGCTCTGCAGTTTTT[A/T]TTTTAGCATGGTGTT | 18519 |
rs51221788 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53667360 | CAATCAGTTCAGAAT[C/T]CTCAAGTTAAATTAG | 18519 |
rs51245120 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Kat2b | Mm_Celera | 17:53657084 | TTGAGAACCATTGCC[A/G]TGATATTTACAGCCT | 18519 |
rs51275377 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53634286 | CATAATAGATACTTA[A/G]AGAGTGGCAAAACCA | 18519 |
rs51292716 | snp | G/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53659935 | AGTTCCTCTGAATCC[G/T]TGGCACCAGGCTTGG | 18519 |
rs51308353 | snp | C/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53623891 | TTATGGAGTCAGACT[C/G]TTTGGAGCTGGTTCA | 18519 |
rs51312091 | snp | A/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53653281 | GTCCAAGGACGAACT[A/G]TTTATTTAGACAGTG | 18519 |
rs51313662 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kat2b | GRCm38.p3 | 17:53651233 | TCTTAAAAATGAACA[C/T]TGATTTATTTAATGT | 18519 |
rs51315891 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Kat2b | Mm_Celera | 17:53613361 | CAACAGCTATTCAAT[A/T]TTCAGTGTACCATGG | 18519 |
rs51329740 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53591815 | CTTAAACTCAGGGTT[C/T]CATCTATGTTAGACA | 18519 |
rs51335509 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kat2b | Mm_Celera | 17:53614636 | CTGCCATGATGGAGA[C/T]TCTTCTACATCTTTG | 18519 |
rs51346422 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kat2b | Mm_Celera | 17:53612624 | ACGACTGGGCTGAGC[C/T]GTGCCCATATTGATT | 18519 |
rs51350941 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53616436 | TTCTTCCAGCACCAG[A/T]GTCATCAGCTTCAAT | 18519 |
rs51358861 | snp | A/G | 0.396694 | 0.202437 | upstream-variant-2KB | Kat2b | Mm_Celera | 17:53565459 | TTGTAGAAACTTGAA[A/G]AACAAACAACCAGAG | 18519 |
rs51385908 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Kat2b | Mm_Celera | 17:53657346 | CTGAAGCAATTCTCT[A/G]GGTATTCTGGAAATT | 18519 |
rs51437919 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53637734 | GCCACATTTTGGCTT[C/T]CCACGATTCAGCAAC | 18519 |
rs51448394 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53586071 | GACTCTTGTGTTGAG[A/G]CAAAAGGAAGAGAAA | 18519 |
rs51480936 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Kat2b | Mm_Celera | 17:53632524 | TTAACATGCTGCATT[G/T]CCATCTTTTCAGGGT | 18519 |
rs51513968 | snp | G/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53667444 | TCCTCTTTTTCCTTG[G/T]GACCTGTTCCCAGTG | 18519 |
rs51528143 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53637174 | TAGGTATTTTATTAG[G/T]TTTTATTACATTTTA | 18519 |
rs51529733 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53650893 | TAGCCTGCTGTGAGT[A/T]TTAAGTCTGGATCAA | 18519 |
rs51549716 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53620780 | CCCCAGACAGGCTTG[A/G]CAGGAGCTGGGACTT | 18519 |
rs51555019 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Kat2b | Mm_Celera | 17:53634936 | GTAAAAATGAGGCAA[A/G]TGGGATTCTCTGTGG | 18519 |
rs51565077 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Kat2b | Mm_Celera | 17:53654413 | AAGATAAAACTCTGA[C/T]TGAACATTATTTTAT | 18519 |
rs51568832 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kat2b | Mm_Celera | 17:53618505 | GGCCTACTCATCACA[A/G]CATTTCTTTCGCTTT | 18519 |
rs51571158 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53670411 | AGATGACTGCTCATG[C/T]TCCTTCTAATGTCAG | 18519 |
rs51573354 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53580721 | CAAGATCTTTCTGTG[G/T]CCTGTTTGGATGTAG | 18519 |
rs51625939 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53668952 | TCAGTTCATAGAATC[C/T]AAGATGACTAGAAGA | 18519 |
rs51639101 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53649670 | CCTAATTTTCAACCT[C/T]TAGGTCCAGTGACCA | 18519 |
rs51640185 | snp | C/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53620426 | CTCGTTTAACACAGG[C/T]CCTCACAAACTCCGT | 18519 |
rs51644460 | snp | A/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53620639 | ACTGTTTTACAGCAC[A/G]GTCTGGATGAGAATC | 18519 |
rs51645715 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53636317 | ACACAGCACAGCTCC[A/G]TTGCCCCCTACATAG | 18519 |
rs51651528 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53653591 | TACAGAGGACAGCAC[A/C]ATATCTGCTATGCCA | 18519 |
rs51698400 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53641523 | AACAGTTGAAACCAC[A/G]TTAAACACAGGAAGT | 18519 |
rs51744571 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53659906 | TCAGAGCAGGGCAAC[A/G]GTGCTGGGAAGAGAG | 18519 |
rs51788449 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53650554 | TAGGGGTTTCGTAAC[C/T]TCATACATGAGCCAG | 18519 |
rs51802094 | snp | A/G | 0.132653 | 0.220748 | utr-variant-5-prime, intron-variant | Kat2b | Mm_Celera | 17:53584162 | TTCTTGGTGTTGGTC[A/G]TGATGAGTCCTGAAA | 18519 |
rs51814563 | snp | C/T | 0.5 | 0 | intron-variant | Kat2b | Mm_Celera | 17:53623537 | ATGAGGCTTTTCTTA[C/T]TATAACTATTTTTTT | 18519 |
rs51819631 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53633525 | GGGTGCATGTAGCCC[A/G]GGTATCCTTGAACTC | 18519 |
rs51834340 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53616042 | TGTATGCACATGGAT[A/G]TGGAAGTTGGATCAA | 18519 |
rs51852959 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53620799 | GAGCTGGGACTTGGC[A/T]CGATTATAAAGTTGA | 18519 |
rs51893451 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53644257 | ATGAAGTTCAGCCTC[C/T]ACGTCCAGTCTTCCT | 18519 |
rs51917147 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53621548 | TACAGTATGTGGCCA[C/T]CTCACTTATGACATC | 18519 |
rs51935670 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53594669 | GTGCCCAGAAAGGCC[A/G]GACGAGAGCATCAGA | 18519 |
rs51966201 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53653966 | TTTTGACCTAGTTAG[C/T]GAGACAGCCTATGTG | 18519 |
rs51968795 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53636384 | GGTGTACAGCAGCAC[A/G]CCATTCATTCCTGCC | 18519 |
rs51981438 | snp | C/T | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53636913 | TAAGAGAGTGTCATC[C/T]AGGCAGTTCATTCAT | 18519 |
rs51996963 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53615750 | TTGGAGTTCTGAACA[A/C]TGTCAGCTGCGGAGG | 18519 |
rs52005814 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53634534 | ACAGTCTGCCAATGT[A/G]GGGTTGTCAAGACTA | 18519 |
rs52014432 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53639648 | ACTCTGTGGTGGCAT[C/T]GGGCTATTTCCTGTT | 18519 |
rs52060493 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53612053 | CTGTCTTACTACTCC[A/G]CCCACGACCTGTAAA | 18519 |
rs52085337 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Kat2b | Mm_Celera | 17:53619269 | TTGTAACGTGACAGA[A/G]AAGCGCCAAGGAACA | 18519 |
rs52122696 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53589669 | AAGGAAGAAAGAAGA[A/G]GAGGAGGAAGAGGAA | 18519 |
rs52144056 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kat2b | Mm_Celera | 17:53610742 | TTACGCTTACATATA[C/T]AGAAATTACTTAGCT | 18519 |
rs52152132 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53599100 | GCACATATTTACGTA[G/T]AACATGATATATATC | 18519 |
rs52154973 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Kat2b | Mm_Celera | 17:53635459 | CCCAGATAGGGGCCA[C/T]ATGTGCAAAATAGTA | 18519 |
rs52160504 | snp | C/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53649270 | ATCATTGCAGAGTCC[C/G]AAACAGATATAATAA | 18519 |
rs52168180 | snp | C/G/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53578960 | GTGTGCGTTCAAGTG[C/G/T]GAGCACGCTTCCTCG | 18519 |
rs52173659 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53669174 | AATAAAAAATGTTTT[G/T]TATATCTGTCTGTAT | 18519 |
rs52197082 | snp | A/C/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53599103 | CATATTTACGTAGAA[A/C/T]ATGATATATATCTAT | 18519 |
rs52198028 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53639582 | TTTTCTTTGTTTCTG[C/T]ACTTTCCATATTTCT | 18519 |
rs52202174 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53649251 | CTCCTGTGAACCTTT[G/T]AGAATCATTGCAGAG | 18519 |
rs52213263 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kat2b | Mm_Celera | 17:53664636 | AATGCCCAGTGGTGC[C/T]AGGTATTTTTCTGTG | 18519 |
rs52245178 | snp | C/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53589989 | AAAATTAGTTTGGAA[C/T]TTTTGAATTTTGAAT | 18519 |
rs52246375 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53589697 | GAAGATGAAGAAGGA[A/G]GAAGAGGAGGAGGAG | 18519 |
rs52262440 | snp | A/C | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53583661 | TTATGAAACCCAAGA[A/C]TTACCTGGGACTTAC | 18519 |
rs52279243 | snp | A/G | 0.32 | 0.24 | intron-variant | Kat2b | Mm_Celera | 17:53649750 | TTAAGAACCAAGCAT[A/G]GAATTCAGTATTCAT | 18519 |
rs52285006 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53612763 | AGTGGCGCAAGTGAC[A/G]AAAGCTAGCTGACTT | 18519 |
rs52325160 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53612769 | GCAAGTGACAAAAGC[C/T]AGCTGACTTGGCTTG | 18519 |
rs52335018 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53590082 | GGTTTGAGAGTAAGG[A/G]ATGTGTGGGGAGAGG | 18519 |
rs52346000 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53669124 | GAAAGAGTTTGAAGA[A/G]CTTTGAACCAACTTC | 18519 |
rs52395225 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kat2b | Mm_Celera | 17:53617303 | GAGGAGGGTTAGCTG[C/T]ATTGAGTTGCATTAA | 18519 |
rs52417739 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53590068 | TTTATAAGAGGAAAG[A/G]TTTGAGAGTAAGGAA | 18519 |
rs52501654 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53668820 | CCAGGACAGCCAGGG[C/T]TATATAGAGAAACCC | 18519 |
rs52522797 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Kat2b | Mm_Celera | 17:53626392 | ATCAAAACAGAAGGC[A/C]TGGCCAGAAACATGT | 18519 |
rs52531388 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kat2b | Mm_Celera | 17:53581631 | AGTCCAGAGTGAACT[C/T]AAACATGCAGTTCTT | 18519 |
rs52539801 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kat2b | Mm_Celera | 17:53612866 | TGGCAGCAGCGCCCT[C/T]ATTTTCCAATACACA | 18519 |
rs52543936 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kat2b | Mm_Celera | 17:53612864 | GTTGGCAGCAGCGCC[A/C]TCATTTTCCAATACA | 18519 |
rs52552242 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53635626 | CTACCTACCTACCTA[C/T]CTATCTATCTATCTA | 18519 |
rs52557267 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53619305 | CCAGAGAGATATCAA[A/G]AATTTTCCTTTCCTT | 18519 |
rs52560925 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Kat2b | Mm_Celera | 17:53578859 | TACCTGAGCAAACCT[C/T]GGAGCTGCAGAGAGA | 18519 |
rs52561687 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Kat2b | Mm_Celera | 17:53626403 | AGGCATGGCCAGAAA[C/G]ATGTGCCCGAGTCTG | 18519 |
rs52564094 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53590045 | TTATTAAAATTTTAT[A/T]TTTTGTGTTTATAAG | 18519 |
rs52567271 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53623183 | CTCTCTCTCTCTCTC[A/T]CACACACACACACAC | 18519 |
rs52573783 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kat2b | Mm_Celera | 17:53614518 | TTGTTTATCCAGGCA[A/G]GGTCTCACCTTGTGC | 18519 |
rs52577188 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Kat2b | Mm_Celera | 17:53636959 | ATGTATCATAAAAAA[A/G]AAGAAAAGTGTGTGT | 18519 |
rs107595654 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53617578 | GCTGGAGAGATGGCT[C/T]AGTGGTTAAGAGCAC | 18519 |
rs107595971 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53615935 | GAGTTACAGTCCGTT[A/G]TGAGCTGCTATGTGG | 18519 |
rs107597707 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53611490 | TGGAAGTAAAGGCGC[A/G]TGCTACCATGCCTCG | 18519 |
rs107599083 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53596499 | CCTTGGATGTGTCTC[C/G]TCTGCATAGATTTGC | 18519 |
rs107599694 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53622114 | GAACATGGCTTGACT[C/T]AAACAACCCACATCT | 18519 |
rs107601305 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53643727 | CTTCAAGCCTGCCTT[C/T]AGTGACGTACCTTCT | 18519 |
rs107602117 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53615850 | TGTATGAGTGTTTTA[C/T]CTTCATGTATGCATT | 18519 |
rs107602804 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53580911 | TCACAGAGATCTGTC[A/T]GCCTCTGCTTCCCAA | 18519 |
rs107605192 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53573142 | AGGTGTTTGTCTCCT[A/G]TGCCAGAGAGTGCCC | 18519 |
rs107606813 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53645023 | CATCGGATCTCATTA[C/T]AAGTGGTTTTGAGCC | 18519 |
rs107607951 | snp | C/G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53639328 | TCCTTTTTTGTTTTT[C/G/T]TTTTTTTTTTTTTTT | 18519 |
rs107608261 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53592721 | TGTTTTTGTTTTTGT[G/T]TTTTAAAGATTTATT | 18519 |
rs107609427 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53643323 | TAAAAACTCAGACAA[A/T]CAAAGCAGTTATAAG | 18519 |
rs107609879 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53616874 | TGCTTTATTGTCCTT[C/T]TGCACAGCACTTTTT | 18519 |
rs107610296 | snp | A/T | | | utr-variant-3-prime | Kat2b | Mm_Celera | 17:53671812 | TGCACTTCCAGAGTT[A/T]TGTTTGTCTGAGGTG | 18519 |
rs107612911 | snp | A/C | | | intron-variant | Kat2b | GRCm38.p3 | 17:53592052 | CCCAAAAAAAAAAAA[A/C]AAAAAAAATTGTGTG | 18519 |
rs107615719 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53618258 | TTCCCTTTACTGAGA[G/T]GAAGGCTCTCTCATT | 18519 |
rs107615962 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53628373 | TGCAAACACACAGTG[C/T]TTACCTTTATTACAG | 18519 |
rs107617009 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53620676 | TTAAGGCAGTGGTGG[A/G]AGGCCAGAAGACCCT | 18519 |
rs107617293 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53591386 | AGTTATTAGATTCTG[C/T]GTTAACTGTCATCTT | 18519 |
rs107617587 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53635653 | TCTATCTATCTATCT[A/G]TCTATCTATCTATCA | 18519 |
rs107617876 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53593740 | TGTCACACCATGAGA[G/T]ATTCTGGGATTGATT | 18519 |
rs107618187 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53573056 | TCTCAGCTAATGAAT[C/T]TACCTATTGATAGAT | 18519 |
rs107620388 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53635537 | TCTGTCTGTCTGTCT[A/G]TCTGTCTGTCTGTCT | 18519 |
rs107620661 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53611942 | TTCAGTTGGAAAGGC[C/T]GCTCTTTTTACACTT | 18519 |
rs107621036 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53581837 | CCTCCTGCTTCTGCA[G/T]CCCAAGTGCTGGGAT | 18519 |
rs107623519 | snp | G/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53615160 | AGAGGCAGGCGGATT[G/T]CTGAGTTCGAGGCCA | 18519 |
rs107624520 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53613469 | CCCAAGGAGCTGAAG[C/G]GGTTTGCAGCCCCAT | 18519 |
rs107624807 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53595182 | TTACTCTGTCATTGA[A/G]GTGTATCCTAACTTC | 18519 |
rs107625641 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53596724 | AGGTGTTTCCAAGGG[A/G]ACCTCTTATCTCTAA | 18519 |
rs107625782 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53647957 | AGACAGGATCTGACA[C/T]CCTCATACAGACATG | 18519 |
rs107625890 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53617878 | CCAGTGACATTCTTC[C/T]TCTAACAGCGTGGCA | 18519 |
rs107626042 | snp | C/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53619324 | TTTCCTTTCCTTTCC[C/T]TTCCCTTTCCCTTCC | 18519 |
rs107626504 | snp | G/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53595204 | CCTAACTTCTTTTAG[G/T]TTTTTTTTTTTTTTT | 18519 |
rs107628228 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53615003 | ACTCTCAGCTCTACC[C/T]GTATCATACCTGCCT | 18519 |
rs107630051 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53613829 | GTGGTTCTCAACTTT[C/T]CTAAAGCTGCAACAC | 18519 |
rs107631358 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53617344 | TGGTTTCATATCTTC[A/G]GCTCTGTGAGTACAG | 18519 |
rs107632890 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53611267 | CCTGGTGGAGGGGGC[A/G]CCCTAGGGCTTTGGT | 18519 |
rs107633685 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53616629 | GGCCGGGGGGCTTTT[A/G]GTCTTTGAAAAATAC | 18519 |
rs107633687 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53600225 | CAGATTATAATTGAG[C/G]ACTACTATGCATGCT | 18519 |
rs107633826 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53646349 | TGTCAAATGCCAGAC[A/G]TGGTTACATCAGACA | 18519 |
rs107634243 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53601037 | GATTTGATTTTTATT[G/T]TTTACTCATTTATTT | 18519 |
rs107635316 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53614342 | CCTTCAGGGGATTTT[G/T]AGCAAGTTCTTTAGG | 18519 |
rs107635684 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53628535 | GGAATTAGAAGCGGT[A/G]TATTTGGTTTGTGGG | 18519 |
rs107636518 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53669984 | AGTCACTTACAACCA[A/G]CCCTCTTTAATTCTA | 18519 |
rs107637424 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53615395 | TAGCTGAAACAGTGC[A/C]GCTTCAGGTTCACTG | 18519 |
rs107637993 | snp | A/G | | | intron-variant | Kat2b | GRCm38.p3 | 17:53592051 | ACCCAAAAAAAAAAA[A/G]AAAAAAAAATTGTGT | 18519 |
rs107639263 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53570837 | CACACCCCAAACCCA[A/G]ACAAAGCCAAACCCC | 18519 |
rs107639932 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53629528 | TCATATACCATTAAG[A/C]TATATTCTAGCCTGA | 18519 |
rs107640923 | snp | C/T | | | upstream-variant-2KB | Kat2b | Mm_Celera | 17:53565838 | CTTTATATACAAGGT[C/T]TCACTGTGTAGCCCT | 18519 |
rs107642789 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53579113 | TTTCTATTTAAAGTA[C/T]CACCCTCCCCTCTTC | 18519 |
rs107646398 | snp | A/G | | | intron-variant | Kat2b | GRCm38.p3 | 17:53619799 | GGATTAAAGGCGTGC[A/G]CCACCACTGCCCGGC | 18519 |
rs107646816 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53593925 | GCTCTTCATAGAAGT[A/G]ACGTCATACAGAGTT | 18519 |
rs107649243 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53626169 | ATCCATGCAGGGTGC[A/G]TTAACAACTGCCTGG | 18519 |
rs107649965 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53586877 | TCCTGCCTGTGAGTT[C/T]TGGCATTGGAGGCAT | 18519 |
rs107652737 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53616155 | GTCACATTTTGTAGT[C/G]CTGGCTGGCCTGGAA | 18519 |
rs107656383 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53634482 | AAGATTTTGGGTTTT[A/G]TTTTCACCTGCCTCC | 18519 |
rs107656805 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53615369 | GGGACTCACTGGCTA[A/G]CCAGCCAGCCTAGCT | 18519 |
rs107660080 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53654170 | TCCCTCCAACCCCTA[G/T]AGCCCGCTGGACATT | 18519 |
rs107660954 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53652677 | GAAGCCAGCAAGCCC[C/T]AGTGACCCTTCTGTC | 18519 |
rs107661859 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53614760 | TGCCTTTCCTCTGAA[A/G]AGAAGAGGGCCTGAG | 18519 |
rs107662604 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53628354 | CATGCTTAATCTTTA[A/G]CACTGCAAACACACA | 18519 |
rs107662996 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53597858 | GACATGAGAAGAGTT[C/T]TTCTAAAGGCCCTCC | 18519 |
rs107666491 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53595576 | CCATCCTCCGACAGA[A/G]TTGTCTTATCAACTT | 18519 |
rs107666954 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53640796 | GGATTAAAGGCGTGC[A/G]CCACCACTGCCTGGC | 18519 |
rs107667410 | snp | A/G | | | intron-variant | Kat2b | GRCm38.p3 | 17:53619740 | TTGTAGACCAGACTG[A/G]CTTTGAACTCAGAAA | 18519 |
rs107667738 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53641041 | GATGCTGTGAGTTAC[C/T]GCGTGTAGTGGTTCT | 18519 |
rs107668031 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53614425 | CATACTGGGCAAGTA[C/T]TCTGCCACTGAGCCA | 18519 |
rs107668343 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53615339 | ATGATAGTAGGCAGA[G/T]ATAGGCAGATCCCAG | 18519 |
rs107671521 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53620077 | TTTTATTTTTTGTGG[G/T]TTACAGGTCCCAAAA | 18519 |
rs107671782 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53627222 | TGCTCTGTAGTTTCC[C/T]CTTCTCTTTGTTCAT | 18519 |
rs107671911 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53586735 | CTGTCCCCATCCCAT[C/T]CCCTTTTCTTCCTTT | 18519 |
rs107672700 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53575883 | GTTACATCTCTGGCC[A/G]CACCCTAAGAGGCAA | 18519 |
rs107673302 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53650055 | GTCAAGGGCTTGTTA[C/T]ATGCCATATTCCATA | 18519 |
rs107674228 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53648571 | TACTATATATATGTA[C/T]ACACACACACACACC | 18519 |
rs107674319 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53662372 | TTACAACGTTCCTCC[C/T]GATCTGCTGGCTCTT | 18519 |
rs107674573 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53571894 | CAGCCCAATGGTTGG[C/T]TGTAAGTGTCTGCAT | 18519 |
rs107679977 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53600460 | GTCTTTTTTTTTTTA[A/T]TTTGGTTTTTTTGTT | 18519 |
rs107680305 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53647412 | GGACAGCCAGGGCTA[C/T]ACAGAGAAACCCTGT | 18519 |
rs107680495 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53581369 | GGACTAACTCTAATT[C/T]TTATTTATCTTCCAA | 18519 |
rs107681970 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53616262 | TTGATTTCTTTTTGA[A/G]ACCAGGTCTCTGGGA | 18519 |
rs107682210 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53571176 | TTTTTTTTTTTTTTT[G/T]CTTTTTTTTTTTTTT | 18519 |
rs107682883 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53634474 | TTACAGGGAAGATTT[C/T]GGGTTTTGTTTTCAC | 18519 |
rs107683009 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53576318 | TTTGCCAGATGGTTC[A/G]TCTAAGATTACCTAT | 18519 |
rs107689926 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53581859 | TGCTGGGATTAAAGG[C/T]GTGCACCACCACTGC | 18519 |
rs107690965 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53590953 | TCTATTCAGGACCCC[A/G]AGGCAGGAGGATTGC | 18519 |
rs107695108 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53582066 | TGTTTTACAAAGGAA[C/G]AAAGTGAAAGTAATT | 18519 |
rs107698881 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53611723 | TCTGTGTAGCCCTGA[C/T]TGTCCTGGAACTCAC | 18519 |
rs107700361 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53584341 | CAGAAATCTGGGGAG[C/T]GGGGGGAACAACAGC | 18519 |
rs107700702 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53616907 | CTGAAGGCTGCCTCC[C/T]CAGCTTCAGATCTGG | 18519 |
rs107702714 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53570381 | TTTCCTGGGGACCAC[C/T]GAAAGAAAACAGAGA | 18519 |
rs107703528 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53617502 | TAATTGTCTTCTTTA[C/T]CTTTCTATTGCTCTG | 18519 |
rs107704495 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53574767 | GCTGGGGTAAAATAA[A/G]TGAACAGTAAAGAGT | 18519 |
rs107705585 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53660858 | TTCTCAGTTTGAGGC[C/T]AGCCTGGTCTACAGA | 18519 |
rs107705930 | snp | C/T | | | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53582432 | AGGGAACTCTTCATT[C/T]AGAGCCTTCTTGGGC | 18519 |
rs107706538 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53613098 | TATACTTGTAAATTC[A/G]CACCTGAAATTAACC | 18519 |
rs107711605 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53621310 | AATGAATGAATGAAT[A/G]AATAAATAATTTGGG | 18519 |
rs107712023 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53572558 | ATTTGCTAGGCAAGC[G/T]CTCTACCTCTGAGCT | 18519 |
rs107714889 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53629916 | AAATGAAGGCTTTGT[G/T]TTTATTTATTTATTT | 18519 |
rs107715781 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53615873 | TATGCATTTGTGTGT[A/C]TGGTGCTGCCAGAGG | 18519 |
rs107716005 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53589469 | TGAACTCAAAAAAAC[C/T]ATCACACAGCTGGAT | 18519 |
rs107716079 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53633012 | CAGGTTTGGTGGCAA[C/G]AACCATTATCCACTG | 18519 |
rs107719727 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53629884 | AAAACGTGCCTTTTC[A/T]TGCTTTTGAGATCTA | 18519 |
rs107720981 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53636705 | GATGGCCCCGATGGT[C/T]AGCTCGCTGCAGACC | 18519 |
rs107721118 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53572422 | CACATGTGATCTAGT[A/G]CAGCTGGTGCAGATG | 18519 |
rs107721161 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53600888 | ATTCTCTGCTGACTG[C/T]ACTCTAAGCCCATTG | 18519 |
rs107721338 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53624990 | GGTGCCCACAAAGGC[C/T]AGAGAGGCTGTTGGA | 18519 |
rs107721383 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53599354 | ACCTTTGAGAATCTC[A/G]CTCTCCAACATGTGG | 18519 |
rs107722252 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53586487 | AGACCAGTCAGAACG[A/G]CATAGAGAAAGCCAG | 18519 |
rs107723590 | snp | C/T | | | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53583524 | TAAAAAAAACAAAGT[C/T]AAATTTGCTAGCCAT | 18519 |
rs107725792 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53578684 | CCACAAGATCTGACG[A/C]TGCACTCTTTTGACC | 18519 |
rs107726668 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53570740 | ACTCATTCCCTACCC[C/T]GGGGAGGGAGCTTAT | 18519 |
rs107730275 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53633050 | TTACTAGCCCTGATG[A/G]TATTTTAGATAAATT | 18519 |
rs107730622 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53633564 | GCCCAGGTGAATTCT[A/G]AGATTACAGGTGTGT | 18519 |
rs107731832 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53581274 | ACTGCAATACAGCCA[C/T]CCCACCCTGTGTCCC | 18519 |
rs107733116 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53621958 | AAACAATGTGTCAAT[C/T]GGTCCTGAAATGATA | 18519 |
rs107736934 | snp | A/C | | | upstream-variant-2KB | Kat2b | Mm_Celera | 17:53566703 | CACACACACACACAC[A/C]CACACACACACCACA | 18519 |
rs107737862 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53575276 | AGCCTGGTCTACAGA[C/G]TGAGTTCCAAGACAG | 18519 |
rs107738892 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53589044 | GGGAATAAAGGCGTG[C/T]GGCACCACCGCCTGG | 18519 |
rs107740928 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53600456 | TCTTGTCTTTTTTTT[A/T]TTAATTTGGTTTTTT | 18519 |
rs107741713 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53628495 | GTCCCCTTTTTTTTT[C/T]TTTGGAGCCTTTGAT | 18519 |
rs107747924 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53628348 | TTGATTCATGCTTAA[C/T]CTTTAACACTGCAAA | 18519 |
rs107756509 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53640442 | CACTGCAACTGAAGT[C/T]TCAGATGTTTGTGAG | 18519 |
rs107758000 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53654890 | ACACACACACACACA[C/T]ACACACACACGCACA | 18519 |
rs107758637 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53642057 | AAACCTCAAAGCCAT[C/T]CCTCAGTGAGTGTAC | 18519 |
rs107758744 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53615349 | GCAGATATAGGCAGA[C/T]CCCAGGGACTCACTG | 18519 |
rs107759538 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53598629 | CTAGAGAACATATAC[C/T]GGGTGCCTCTCCTCT | 18519 |
rs107761603 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53652683 | AGCAAGCCCTAGTGA[C/G]CCTTCTGTCTATGCC | 18519 |
rs107762081 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53637959 | CTCTGTACCTTACTC[A/G]TGCTATCTCATTCTC | 18519 |
rs107765821 | snp | A/G | | | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53584066 | GGAGATAGCTGATAG[A/G]CTGTCGGGTAAGAGA | 18519 |
rs107766050 | snp | C/T | | | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53583189 | GATTTTCTGTGAGTT[C/T]AAGGCCAGCCTGGTC | 18519 |
rs107767302 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53643716 | AGGCTGTAAACCTTC[A/G]AGCCTGCCTTTAGTG | 18519 |
rs107771882 | snp | A/G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53616118 | TTTATTTGTTTTTTT[A/G/T]TTTTTTTGTTTTTGA | 18519 |
rs107772501 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53613097 | TTATACTTGTAAATT[C/T]ACACCTGAAATTAAC | 18519 |
rs107774813 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53633571 | TGAATTCTGAGATTA[C/T]AGGTGTGTACCACCA | 18519 |
rs107776719 | snp | A/C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53589996 | GTTTGGAACTTTTGA[A/C/T]TTTTGAATAGAACAA | 18519 |
rs107778819 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53634951 | GTGGGATTCTCTGTG[A/G]TGAATAAAGGTCTGA | 18519 |
rs107780250 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53623798 | AAGAAGATTACAGAG[A/G]CTGCTTTGGCCTCTG | 18519 |
rs107780333 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53593361 | AACAAAACTTAGCTT[A/G]TAAAATGAATGAACA | 18519 |
rs107782836 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53643154 | ACTATTCAGTGAGAA[A/G]TGTCAGTGAATGACC | 18519 |
rs107783123 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53656169 | CTGCCCAACACCCCT[C/T]CCCCTGCTTCCCTCC | 18519 |
rs107786267 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53640394 | TGCACCACGTGCATG[C/T]GTGGTGTCCATAGAA | 18519 |
rs107787776 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53581378 | CTAATTTTTATTTAT[C/T]TTCCAAGGATGAGGC | 18519 |
rs107788987 | snp | A/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53595797 | CCACGAGTCATTATC[A/T]CTGGCCTTTTGACTT | 18519 |
rs107790263 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53589011 | CAGAAATCCGCCTGC[C/T]TCTGCCTCCCAAGTG | 18519 |
rs107790584 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53593928 | CTTCATAGAAGTGAC[A/G]TCATACAGAGTTTGT | 18519 |
rs107791288 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53636242 | CCATTCTCCTGCCTT[A/G]GCCTACCATGTAAGG | 18519 |
rs107791754 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53600319 | GAGCCACAGCCCTAG[C/G]AGGCTTTCTCTTTAT | 18519 |
rs107794048 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53592668 | AGAGAAAGAGACTAA[C/T]GGGGAGAGGCGTTGT | 18519 |
rs107797321 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53618183 | TGTGTATGTGTGTGT[A/G]TGTTTGCGTGTGTAA | 18519 |
rs107797788 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53652350 | TTTCCTGTCCCTGGG[C/G]AAGCTGAGGTAGGAA | 18519 |
rs107798513 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53575618 | AATAAATACCTAATT[A/T]AAAAAAAAAGGAAAA | 18519 |
rs107799268 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53590122 | ATCCTTCCAACCATG[A/G]TGGCGTGAAGGAGCC | 18519 |
rs107799500 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53612512 | GCTTATAGTATGCCA[A/G]GATTATCGCCCATCT | 18519 |
rs107800186 | snp | G/T | | | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53583345 | TGGCACATGCCTTTA[G/T]TCTCCGCATTCTAGA | 18519 |
rs107801624 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53626413 | AGAAACATGTGCCCG[A/T]GTCTGTATTTTCTTT | 18519 |
rs107802056 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53621261 | AAGCTCAAGGCCAGC[A/C]TGGATTACATACTGA | 18519 |
rs107802368 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53669577 | CAACCTTGTATCAGG[A/T]CATACTTCTGCGCTC | 18519 |
rs107802553 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53652408 | ACAGAGCAAGACCCT[A/G]TCTCAGAACAACAAC | 18519 |
rs107802741 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53598797 | TCCCTCTTTTTTCTC[C/T]CCAACCTTCCCTCCT | 18519 |
rs107804128 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53615083 | CTGTAAGGCAGCCCC[A/T]ATTAAATGTTGTCCT | 18519 |
rs107805011 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53584279 | TGTGTAGAACTGGAG[A/G]GCTTGGGAGGATGGT | 18519 |
rs107806636 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53627220 | TTTGCTCTGTAGTTT[C/T]CCCTTCTCTTTGTTC | 18519 |
rs107811114 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53651915 | CCAAGTGTGTGTATT[C/T]TGTAGGACCCACACT | 18519 |
rs107811312 | snp | A/G | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | Kat2b | Mm_Celera | 17:53567305 | CGCGGGGACCCTGGC[A/G]GCTGCGGGTGACAGT | 18519 |
rs107811877 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53590722 | AGGACAGCCAGGGCT[A/G]CACAGAGAAACCCTG | 18519 |
rs107811887 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53613719 | GGGGGTGGGATAGGA[G/T]GTTTTCACAGGGGAA | 18519 |
rs107812478 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53636505 | GAAGAGGGGGGTTTG[C/T]GCAATGACACATTCC | 18519 |
rs107812715 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53600361 | CATTGTGGGGACTCT[C/T]TCATCCTGCCTTGCA | 18519 |
rs107816246 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53636010 | CTCGCTTCTCCCCAA[A/G]GAGTGACTCATGCTT | 18519 |
rs107816647 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53657652 | AGAGATAGGCAGAGA[G/T]AGGCAGAGAGGCAGA | 18519 |
rs107818323 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53617662 | CACAACCATCTGTAA[A/G]GGGATCTGATGCCCT | 18519 |
rs107819816 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53642063 | CAAAGCCATCCCTCA[A/G]TGAGTGTACTGCCTT | 18519 |
rs107822250 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53580804 | TGTTATTGTTGTTTT[C/G]TTTTTGTTTGATTGT | 18519 |
rs107823237 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53661370 | GACAGCAGTCATTCA[C/T]TGAGTGTTTTATTTA | 18519 |
rs107824113 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53623305 | AGGCTACTTAGTGGG[A/C]CGATGTCTCAGACAA | 18519 |
rs107825406 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53629114 | GTGTACGCATGCGTG[C/T]TTTAAATGCTAGATA | 18519 |
rs107826988 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53622587 | ACAGTTGGTTATGGA[C/T]CTTTATGTGGGTGCT | 18519 |
rs107827764 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53614700 | TTCAATCAAGTGTTA[A/G]GAAATAATTATTCAC | 18519 |
rs107828549 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53647660 | AGTCTTTGACATCTA[C/T]GATCATAGAAATGTA | 18519 |
rs107830997 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53601038 | ATTTGATTTTTATTG[G/T]TTACTCATTTATTTT | 18519 |
rs107831276 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53614260 | ATAGTTTAACAAACT[A/G]TCTTGGACCCATCAC | 18519 |
rs107831296 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53624776 | TAATTTTTGTTTTTC[A/G]AGACAGGGTTTCTCT | 18519 |
rs107832123 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53575048 | TTACATTGGTACTTC[G/T]CCTGATCACAAACAC | 18519 |
rs107833219 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53633395 | TTAGAAAACAATTCT[A/G]CATGTTCATTTTCCA | 18519 |
rs107833729 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53575176 | GATTAGGATTTTAGG[A/G]GCCAGCCGTGGTGGC | 18519 |
rs107834154 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53635290 | CCTATCTCAAAACCA[A/G]CCAACCAACCAGCCA | 18519 |
rs107834238 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53580705 | ACAGAGCAAAACAGA[A/G]CAAGATCTTTCTGTG | 18519 |
rs107835661 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53579473 | ACTGTTCTCCCTCTC[C/T]CTCTCTCACTCTCTC | 18519 |
rs107835832 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53581181 | TACTTCAGAATTGTT[C/T]GGCCCACCACACCTG | 18519 |
rs107836002 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53639703 | TGCGGTTGGTTGCCT[C/T]AGTGTGTTGTGAAGT | 18519 |
rs107836587 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53643340 | AAAGCAGTTATAAGC[A/T]TAACAGAGCATTGGA | 18519 |
rs107839036 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53635871 | ATCCAACACTGTGTT[C/T]CTCCTCAGGCACTAG | 18519 |
rs107839853 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53647796 | AAACGAACAAACAAA[C/T]AAACAAACATAAAAA | 18519 |
rs107839941 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53601081 | TGTTTTGCCTGCATG[C/T]ATACCTGGTGCCCGA | 18519 |
rs107841116 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53637737 | ACATTTTGGCTTCCC[A/C]CGATTCAGCAACCCA | 18519 |
rs107841281 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53651708 | TATTCTATACTAGTG[C/T]GTCTGTGTCTGCTTA | 18519 |
rs107841766 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53627452 | CCCTTAGGTGGCAGC[G/T]TGTGGACATAGCTGT | 18519 |
rs107845893 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53621148 | AGGAAAGTTACTGTT[C/T]AAAGGTGGTTGTGGT | 18519 |
rs107849089 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53646724 | GTCGGTGGCAGTGCA[C/T]GCCTTTAAATCCAAC | 18519 |
rs107849718 | snp | A/C/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53619568 | GTTGTCTTGGAACTC[A/C/T]TTATGTAGACCAGGT | 18519 |
rs107850730 | snp | C/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53652467 | AAAATATAATGCACA[C/T]GCACTTATTAACTTT | 18519 |
rs107852145 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53618232 | CTCTGAGTAGACCCA[C/G]ACCCTCAACCTTCCC | 18519 |
rs107853438 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53641130 | CTCTTCCAAGATGGT[C/T]TTTGAGCCTTGAGGA | 18519 |
rs107853517 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53640154 | GGGTAAAGGAGATGT[C/T]TATAGAGACACAATC | 18519 |
rs107855913 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53568276 | TTTGGGGACTTTAGG[C/T]ACCCAGGGCATCCAG | 18519 |
rs107858016 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53589799 | TGTGTTTCATCCATC[C/T]TCACTGTCTGATAGT | 18519 |
rs107859024 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53612780 | AAGCTAGCTGACTTG[A/G]CTTGCTTTCCTTTCC | 18519 |
rs107859153 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53579460 | GTATGAACTGCTCAC[C/T]GTTCTCCCTCTCCCT | 18519 |
rs107860294 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53642651 | GCCAGTCAGGAGTGA[A/G]CTGTCATCTCCTGTT | 18519 |
rs107861408 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53623147 | ATGTCTCTCTCTCTC[C/T]CTCTCTCTCTCTCTC | 18519 |
rs107861712 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53622624 | TGAACCTGGGTCCTG[A/G]AAAAGCAAACAGTCC | 18519 |
rs107863649 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53670045 | CTCAGAGAGCACTAG[A/G]CATGGATGTGGCACA | 18519 |
rs107865607 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53617972 | CTTTTTCTAGCATGG[A/T]GTATGTGACAATGTT | 18519 |
rs107866687 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53594343 | AAGGACATTCCTGCT[G/T]CAATTTCTTAAAATA | 18519 |
rs107867519 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53642135 | ATTGCACTACCAGCC[A/G]GGAACCGATTGTTTA | 18519 |
rs107867547 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53637349 | TTTATTTATTTATTT[A/T]CAGTTCTGGGCTCAA | 18519 |
rs107869210 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53632225 | AGAAACAATTATCCC[A/G]GAACCTCATTTATTT | 18519 |
rs107871047 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53597755 | AAAAAGAAATAAACC[C/T]GTGTAGTAAAATATA | 18519 |
rs107874333 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53626825 | CTCTGGTCACACTCT[C/G]TTTTTCTCTGTAGTG | 18519 |
rs107875176 | snp | C/G/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53614900 | CTTGTTGGAGTAGAC[C/G/T]TGTCGTTGTGGGCGT | 18519 |
rs107878117 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53575146 | CAGTTTATGATAAGT[C/T]AGTAGCTTTTATAAG | 18519 |
rs107878814 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53646331 | GACTTTGTTTTTATA[C/G]TATGTCAAATGCCAG | 18519 |
rs107879095 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53625035 | AGTTGTAGGTAGTTG[C/G]GAACTATCCAACATA | 18519 |
rs107882177 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53622489 | ATGTATGGCTATTTT[G/T]CCTTTTTATATTGTC | 18519 |
rs107882568 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53585880 | GTCAGTGCTCCCAAC[C/T]GCTGAGCCACTTCTC | 18519 |
rs107884516 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53633977 | CGAGCGATATTGCCA[A/T]ATTTTAGAAAACAAA | 18519 |
rs107884949 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53596869 | GAAATTCACTGGTTT[G/T]TTTTTTTTTTTTTAA | 18519 |
rs107885317 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53657763 | GGCAGAGAGGCAGAG[A/G]GAGAGGCAGAGAGGC | 18519 |
rs107886160 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53617013 | CCTTCCTTTCTTTTT[C/T]TTTGGGGCCAGGGAA | 18519 |
rs107888721 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53570882 | TCACAAGGCTCTCTC[A/G]GAGTTTAGTATTGAT | 18519 |
rs107890305 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53587104 | GCCTTTTGGAACCCC[A/C]TCCCCATTGCTGTGC | 18519 |
rs107893046 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53611458 | AGGAGATCTGCCTGC[C/T]GCTGCTTTCCAAGTG | 18519 |
rs107893168 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53591849 | CTTCTACCTCTGGGC[C/T]ATAGCCACACTATAG | 18519 |
rs107896033 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53589292 | TAAAAAATCCTCTTA[C/G]TGTACTGACTGGGCA | 18519 |
rs107896041 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53613806 | AGAACATAGAACACT[A/G]TAAAGGGGTGGTTCT | 18519 |
rs107897423 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53613161 | GTTAAAAGAATTTTA[C/T]ACTCACTTAAGTGTA | 18519 |
rs107897444 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53625105 | AAGTGATCTTAATCA[C/T]GTAACCATCTCTCCA | 18519 |
rs107897747 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53613576 | GGATGGATCCATGGT[A/G]GCAGAGGATGGCCTT | 18519 |
rs107898172 | snp | C/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53614886 | GGAGTAGGTGTGGCC[C/T]TGTTGGAGTAGACGT | 18519 |
rs107898683 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53572801 | TAGCAGAAGCAGAAG[A/G]GCCAAAGGCCCTGTG | 18519 |
rs107902268 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53601148 | GAGTTACAGAAGACT[C/G]TAAGCTACCATATGG | 18519 |
rs107905012 | snp | A/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53619528 | GTTTTTGTATTTTTG[A/T]AACAGTGTTTTCCTG | 18519 |
rs107905347 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53647996 | CAAAATAGCAATGTA[C/T]ACAACATAAAAGTAA | 18519 |
rs107906660 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53584580 | TCTTGGTAGCCGGCA[C/G]GGCACTGTTCACCAA | 18519 |
rs107907394 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53601029 | TTTATTTTGATTTGA[C/T]TTTTATTGTTTACTC | 18519 |
rs107907739 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53617493 | AACTAGATGTAATTG[G/T]CTTCTTTATCTTTCT | 18519 |
rs107908595 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53621294 | CAGTGTCTCAACAAT[G/T]AATGAATGAATGAAT | 18519 |
rs107909989 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53640067 | ACATAGACAGCTGGA[A/G]TCTGCTGTGCATCTC | 18519 |
rs107910021 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53620712 | ATTACTGCTTCACTG[A/T]GCTGATGAGACTTCT | 18519 |
rs107911481 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53652472 | ATAATGCACATGCAC[A/T]TATTAACTTTTCATA | 18519 |
rs107911797 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53643584 | TTTGGCTTGCTCTTC[C/T]GAGGGCAATAGTCCA | 18519 |
rs107912617 | snp | G/T | | | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53582245 | GACTGTTAGCTAATC[G/T]GCAAAAAGTGGGGGA | 18519 |
rs107915373 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53640618 | ATTTTCATCTCCACA[A/C]ACTCCTCCCAGATCC | 18519 |
rs107916132 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53595238 | TTTTGGTTTTTTGAG[A/G]CAGGGTTTCTCTGTG | 18519 |
rs107916446 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53611251 | TACAGGCCTGATTTG[A/T]CCTGGTGGAGGGGGC | 18519 |
rs107918116 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53599078 | GGACAGGGAGATGTG[G/T]GTGTGTGCACATATT | 18519 |
rs107919067 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53637576 | GGCCAGTGAGATGTG[A/G]TATACACATTTTTCA | 18519 |
rs107922526 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53613826 | GGGGTGGTTCTCAAC[C/T]TTTCTAAAGCTGCAA | 18519 |
rs107923420 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53656554 | CTGGAGCACACTGCA[C/T]AGCCTGCAGGCAGCT | 18519 |
rs107924332 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53644332 | AAAGCGCAAACATCT[G/T]TCCTTATTGACTTCG | 18519 |
rs107924339 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53633221 | ACCAGCTTAGTCTAC[A/T]TTAGTGAGTTCCATA | 18519 |
rs107931239 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53621149 | GGAAAGTTACTGTTC[A/G]AAGGTGGTTGTGGTG | 18519 |
rs107934395 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53633241 | TGAGTTCCATATTAT[A/G]TGCTCAACCAATGCT | 18519 |
rs107935257 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53622292 | GTGATTAACTTATCT[A/C]TGGACTCTAAGCATT | 18519 |
rs107935504 | snp | C/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53615275 | AAAAAAAATGTTGTC[C/T]TTTATAAGAGTTGAC | 18519 |
rs107937199 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53595237 | TTTTTGGTTTTTTGA[A/G]ACAGGGTTTCTCTGT | 18519 |
rs107937469 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53644185 | CGCTTCAGGGAAAAT[C/T]CATCCTGGGAAGAAC | 18519 |
rs107939053 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53613546 | GGACTAAACCACCAA[C/T]CAAAGAGTACACATG | 18519 |
rs107940468 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53648451 | CACACACATATATAT[A/G]TGTGTGTGTGTGTCT | 18519 |
rs107943731 | snp | G/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53593173 | GTACACATAATACAC[G/T]TAGGCACACACATAT | 18519 |
rs107945295 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53578563 | TATGTCATTTGCAAA[A/T]GAGGGGAGGCGTGAG | 18519 |
rs107946882 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53625755 | TGTAATGGGATCTGA[C/T]GTCCTCTTCTGGTGT | 18519 |
rs107950022 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53599715 | TCTACAGTATGGGCT[C/T]TGGGGTTCAGGCTCA | 18519 |
rs107950175 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53626823 | CTCTCTGGTCACACT[C/T]TCTTTTTCTCTGTAG | 18519 |
rs107950219 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53632968 | CGGCTCTCTCTACCA[C/T]GTGATACAGAGAAAT | 18519 |
rs107951249 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53626656 | TTTTTTTTTTTTTTT[C/T]TTTTGGAGACATGGT | 18519 |
rs107955071 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53573613 | GGCCGGTGAGGAAAC[A/T]TAAGCTATACTTAAC | 18519 |
rs107960322 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53647311 | GGCCGGGCGTGGTGG[C/T]GCACATCTTTAATCC | 18519 |
rs107961461 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53573655 | TGACCTGAGGGAGGT[A/G]GATCCAAGTCTTATG | 18519 |
rs107962908 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53640886 | TTGTGGGGATATCCA[A/C]TGGAACATGGTTGAC | 18519 |
rs107964131 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53634037 | TAATCAAAGCACTTG[A/G]GAGGCAGATCTCTGA | 18519 |
rs107964669 | snp | A/G | | | intron-variant | Kat2b | GRCm38.p3 | 17:53589948 | GAGAAACCCTGTCTC[A/G]AAAAACCAAAAAAAA | 18519 |
rs107966030 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53590876 | GATAAAAGTGTGTGT[A/G]TGTGTGTGTGTTTGT | 18519 |
rs107967005 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53624006 | CAGCCCCCGTACACA[C/T]GCATAGGTGTGAACA | 18519 |
rs107967146 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53614423 | TTCATACTGGGCAAG[C/T]ATTCTGCCACTGAGC | 18519 |
rs107970877 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53579193 | GCAGAAGCATTTTTT[A/T]TTTTTTTTTGGTCAT | 18519 |
rs107971269 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53665986 | CTGGCTAAGGTGGAC[G/T]TGTTGACTTCTGTGA | 18519 |
rs107973638 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53594715 | GTTAGACAGCTGGTG[C/T]GTTGCCTTCTGTGAG | 18519 |
rs107974592 | snp | A/C | | | intron-variant | Kat2b | GRCm38.p3 | 17:53570827 | CACACACACACACAC[A/C]CCAAACCCAAACAAA | 18519 |
rs107974837 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53567722 | TGCGGCTTGCACAGC[A/G]TCTCACTGGGACAGG | 18519 |
rs107974884 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53623850 | GAGTGTGTGTGTGTG[A/T]GTGTGTGTGTGTGTG | 18519 |
rs107976590 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53631852 | TTACAAATACATGAC[G/T]TTTTGTAAGAATAAT | 18519 |
rs107980370 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53570893 | TCTCAGAGTTTAGTA[G/T]TGATCTCACGTGCAC | 18519 |
rs107981184 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53588422 | ACAATACACTTTAGT[G/T]CAGCAGTGTTTTTGA | 18519 |
rs107981879 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53635835 | CTCATAACCACCTGT[A/G]TGTAACTCCAGTTCC | 18519 |
rs107984059 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53635627 | TACCTACCTACCTAC[C/T]TATCTATCTATCTAT | 18519 |
rs107986052 | snp | A/C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53576958 | GTCTTGCTATTCGCC[A/C/G]TACACGGGAGGTTAT | 18519 |
rs107989095 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53628127 | TCCCAAGGGGCTGAG[A/C]TAGGAAAGAAGATCT | 18519 |
rs107989156 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53643847 | CATTTGTCACTCAAA[G/T]TACCACACCTAGCCT | 18519 |
rs107995547 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53570692 | GGTCTCACACGTTTT[C/T]CTCTGGGATCTGAAA | 18519 |
rs107996361 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53568765 | TTTGGAATCGCTAAA[A/T]GCAAAAATCAGGAGG | 18519 |
rs107997408 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53570683 | TCCACCTCAGGTCTC[A/G]CACGTTTTTCTCTGG | 18519 |
rs108001116 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53647766 | CTCTATGTCAAAAAA[A/C]AAACAACAAACAACA | 18519 |
rs108002859 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53578461 | CAACTTTGTGGAACT[A/C]GTCTTCTCCTACTTT | 18519 |
rs108004324 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53585040 | TGTTTCCTGTGCTGG[A/G]AATGGAAAAGGATGG | 18519 |
rs108005412 | snp | A/G | | | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53584069 | GATAGCTGATAGGCT[A/G]TCGGGTAAGAGAGGT | 18519 |
rs108007304 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53637203 | TATTTATGGTGTGTG[C/T]GTGAAATGTTGGCAG | 18519 |
rs108017350 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53636206 | CCCTTCCCTGGATAG[C/T]TCAGATTGGTGTTGA | 18519 |
rs108017462 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53571873 | CATTGGGCTGAGGTC[A/T]GTGACCCTTATGGAA | 18519 |
rs108025621 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53613195 | TATTTACTCTCTGAC[A/G]CTGTAATACATAACT | 18519 |
rs108029176 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53640327 | ATTTTATTTATTTAT[G/T]TAGAAAGTTTTTATT | 18519 |
rs108029940 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53662291 | GGTAAGCACAACTTG[G/T]GTGAGTTCACGTGTG | 18519 |
rs108030082 | snp | A/G | | | intron-variant | Kat2b | GRCm38.p3 | 17:53616110 | TGCTTCTTTTTATTT[A/G]TTTTTTTGTTTTTTT | 18519 |
rs108031716 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53574646 | TCCCTTGGCAGGCAA[G/T]GCCTTTGGGACAGTC | 18519 |
rs108036684 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53600073 | CACAGAGACCCACCT[A/G]CTTTTACTTCCATAG | 18519 |
rs108042922 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53616503 | TAATATTATGTTCAT[C/T]ATTTCAGTCTTTCTA | 18519 |
rs108043927 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53611991 | AATCTGGCTTACTGT[C/T]GAGTATGGCAAGGAC | 18519 |
rs108046504 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53620136 | AAGTGATTGTGATTG[A/G]GGGAATGTATGGTGT | 18519 |
rs108048242 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53620687 | GTGGAAGGCCAGAAG[A/G]CCCTTCCACATTACT | 18519 |
rs108048392 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53586901 | GAGGCATAGACCACC[A/G]TGCACAGCTTTATAA | 18519 |
rs108049086 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53646856 | AACAACAGACAGACA[A/G]ACAAACAAGAAACTC | 18519 |
rs108051016 | snp | G/T | | | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53583142 | TGGTAGCATACACCT[G/T]CAGTCCCAACACTGA | 18519 |
rs108051147 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53585353 | ACACACACACACACA[C/T]ACACACATTTCCTGA | 18519 |
rs108057760 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53648718 | ACCATCCATTTTTTT[C/T]CTTTTGCCTTTTATT | 18519 |
rs108060985 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53634120 | CACTGTCTGCAAAAA[A/C]AAAACCAAAAACCAA | 18519 |
rs108061535 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53614483 | ATCTATCTATCTATC[G/T]ATCTATCTATCTATC | 18519 |
rs108061683 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53625435 | CAGAACTGGACAGCT[C/T]GATTCACGTACACTC | 18519 |
rs108066746 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53600705 | GGCTCAGCACTCTAT[C/T]ACAGTGGCTTAAATA | 18519 |
rs108067394 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53615605 | TTCTCAGAGCTACAT[G/T]ATGAGACTCTGCCCT | 18519 |
rs108067560 | snp | C/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53614899 | CCTTGTTGGAGTAGA[C/T]GTGTCGTTGTGGGCG | 18519 |
rs108068535 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53584794 | GTGTGCCCAAGCCAT[A/T]GCTTACATGTGGAGG | 18519 |
rs108069446 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53616691 | AGTGTCTCATGTAAT[G/T]TTGGATGGTCTTGAA | 18519 |
rs108071362 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53666844 | GACCTGGAGATCACC[A/G]GGCAGACTAGGCTGG | 18519 |
rs108074016 | snp | C/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53593596 | AAGTTGTGTGCTCCC[C/T]ACCCCCTTATTTCTT | 18519 |
rs108075730 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53577816 | ATTTTAATTCGGGCT[C/G]ATTAGGAGTTTAAGA | 18519 |
rs108075831 | snp | C/T | | | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53582333 | AAAGTTTCTCATAGT[C/T]CCCGTACTTTATTTT | 18519 |
rs108077486 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53584585 | GTAGCCGGCAGGGCA[C/T]TGTTCACCAAGAGTG | 18519 |
rs108078268 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53644084 | TCTAGACTATTAAGC[A/T]CCCCTAGAGGCTGTG | 18519 |
rs108079217 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53600606 | ATGTGTGTGACTATA[G/T]CATATGTATATATTC | 18519 |
rs108079941 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53666604 | CTGGGCCTGATAAGC[A/G]TTTTTGGAACCCCAA | 18519 |
rs108081043 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53634533 | CACAGTCTGCCAATG[A/T]AGGGTTGTCAAGACT | 18519 |
rs108081076 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53631934 | TGTATAGCTCTGGCT[A/G]TCTTGGAACTCACTG | 18519 |
rs108084275 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53632451 | ATCTTTTTTTTTTTT[G/T]CTAATAACCACTGAG | 18519 |
rs108086052 | snp | A/G/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53644322 | CTTTTTTTTAAAAGC[A/G/T]CAAACATCTTTCCTT | 18519 |
rs108086801 | snp | C/G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53634351 | CTGGTCCCACCTTCC[C/G/T]CTATCTGTGTGAGCT | 18519 |
rs108090704 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53579499 | CTCTCTCTCTCTCTC[C/T]CTCTCTCTCTCTCTC | 18519 |
rs108090910 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53571620 | TTTTCAAGCTCTCCC[C/T]CCCACCCCTTCCCTG | 18519 |
rs108092254 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53632916 | TCTCTCTGCCCTGCC[A/C]TGTATGTGGGGGTTG | 18519 |
rs108092976 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53593018 | GGGAGCTGGAGAGAT[A/G]GCTCAGTAAGAAAAC | 18519 |
rs108094118 | snp | C/T | | | upstream-variant-2KB | Kat2b | Mm_Celera | 17:53565923 | GGCCAGTCTCTGCTT[C/T]TGCAGTTCTGGGGTC | 18519 |
rs108094511 | snp | A/G | | | upstream-variant-2KB | Kat2b | GRCm38.p3 | 17:53565748 | GACCTCGAACTCAGA[A/G]ATCCACTTGCCTCTG | 18519 |
rs108094524 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53622506 | CTTTTTATATTGTCT[A/G]TGCACCACATGTGTG | 18519 |
rs108094885 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53599968 | ATTACCCCTCTTCCT[C/T]TTTCTTTTTCTTTTT | 18519 |
rs108095350 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53570749 | CTACCCCGGGGAGGG[A/G]GCTTATCACAAGGCT | 18519 |
rs108096817 | snp | A/G | | | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53582542 | AAACAAAACAAAACA[A/G]TGAACAGTGTTCTCT | 18519 |
rs108100554 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53600554 | AACTCCTGGAGTAAT[G/T]AAATTAATCAGTTTT | 18519 |
rs108102550 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53596639 | CTGTTATTGAGTTAA[A/G]GCTGCTAGGCTAACC | 18519 |
rs108102865 | snp | C/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53595052 | CTTGAAATTCTCTTC[C/T]TCTTCCTCCTCCTCC | 18519 |
rs108103926 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53571177 | TTTTTTTTTTTTTTG[C/T]TTTTTTTTTTTTTTT | 18519 |
rs108109410 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53647596 | TGCTAGGAAGAAATT[A/G]GAGATTTAATAACAA | 18519 |
rs108109412 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53616225 | GATTGCAGGTGTGTG[C/T]CCCCCCCACCCCAGA | 18519 |
rs108109589 | snp | A/G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53594529 | TGCTAATGAGGCTGC[A/G/T]GGACACCCCAGTAGG | 18519 |
rs108111785 | snp | A/C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53599465 | TTTTTGGTGTGTTTT[A/C/T]GACAGAGCTTTGCTG | 18519 |
rs108117607 | snp | C/G/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53569904 | TTAGAACTTTTGGCC[C/G/T]GTTGGAGTTGGGTGG | 18519 |
rs108118774 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53568141 | TCATTATTGTTATTA[C/T]TTATTTAGCGAAAGC | 18519 |
rs108118995 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53668962 | GAATCTAAGATGACT[A/G]GAAGAAGAAAGACGT | 18519 |
rs108121247 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53622609 | GTGGGTGCTGGCAAT[C/T]GAACCTGGGTCCTGG | 18519 |
rs108123751 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53572421 | CCACATGTGATCTAG[C/T]GCAGCTGGTGCAGAT | 18519 |
rs108124387 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53577125 | GAGCCTTGGAACATC[C/T]CTAGGCACATGCCTC | 18519 |
rs108125714 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53585590 | AGACAGGGTATAATA[G/T]CCCTGGTGTTCTGGA | 18519 |
rs108126626 | snp | A/C | | | downstream-variant-500B | Kat2b | Mm_Celera | 17:53673012 | CTATTCTCCACAGGC[A/C]TCCATACTCATGCGC | 18519 |
rs108127842 | snp | A/G | | | intron-variant | Kat2b | GRCm38.p3 | 17:53615259 | AAAAAAGAAAAAAAA[A/G]AAAAAAAATGTTGTC | 18519 |
rs108130013 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53637415 | CCTCTGAGCTACATC[C/T]CAAACCCACTTTATA | 18519 |
rs108130499 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53568582 | GGTAGATGACTTCCC[C/T]TCCGGGACATTCTGG | 18519 |
rs108130509 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53580973 | CCACAGGTTTTGATT[C/T]TGAGAGACATTATGT | 18519 |
rs108137200 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53581001 | TGTAGCCCTGGTTGG[C/T]CTGTAACTCATAGGG | 18519 |
rs108138529 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53669188 | TTTATATCTGTCTGT[A/C]TATGTATTTATATAT | 18519 |
rs108138983 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53612275 | CCCCGGAAGCTGCTG[A/C]ACTGGAAAGCTCTCC | 18519 |
rs108139566 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53599955 | ACCAAACTGAGCTAT[C/T]ACCCCTCTTCCTTTT | 18519 |
rs108139719 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53575520 | ATGCCTCAGTACAGG[A/G]GAATGCCAGGGCCAA | 18519 |
rs108139964 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53586526 | AGTCAGCCAACCAAC[A/C]GACCAAAATAAACCT | 18519 |
rs108144792 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53636994 | GTGTGTGTGTGTGTG[A/T]ATGTGTGTGTGTGTG | 18519 |
rs108148603 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53643379 | AAATGACACACTTGA[C/T]ATTAAATAAGAATTG | 18519 |
rs108152758 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53595870 | ACAATACAATTCCCA[G/T]TGCCTCCTCACCCCT | 18519 |
rs108155153 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53580097 | TTACAAACTGGAACC[C/G]AGTTAAAAGTATACT | 18519 |
rs108158438 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53632943 | GTTGTAGAAACAGGC[A/T]TGTAGGGATCGGCTC | 18519 |
rs108158461 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53610610 | AGCAAAATGTTTGAG[C/T]TGTAGTTACAACCAG | 18519 |
rs108159026 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53578348 | CTATAAGACAAAAGC[C/T]ACCACTGTGTGTGCG | 18519 |
rs108160919 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53637457 | AATTTTTTTTTTTTT[A/T]TTTTTTTTAGTTTTA | 18519 |
rs108170262 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53596432 | GTCCAGGAGCCTCTC[A/G]TGTGAACAAAGCCAC | 18519 |
rs108171136 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53635890 | CTCAGGCACTAGGCA[C/T]ACATGGTGCATATAC | 18519 |
rs108171143 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53649937 | TTTCTTTTTTTTTTC[C/T]TGGACTGGTCTCATG | 18519 |
rs108171280 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53623404 | TTAACCCGGCACAGG[G/T]GAGTTCAGCGGGATG | 18519 |
rs108171320 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53644070 | GCATTTTAATAATCT[C/G]TAGACTATTAAGCAC | 18519 |
rs108173664 | snp | C/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53662597 | TCTGTTTTTTTTTTT[C/T]TTATTCTTCATTCTT | 18519 |
rs108174351 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53595149 | TGGGCTGATCCTTAG[G/T]CCTTTCATGTGCTGC | 18519 |
rs108177369 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53633918 | GTTTGGAGGTTTGAG[A/G]TAGAATGGAAGGAGA | 18519 |
rs108177558 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53628175 | AAACACAGGGACTGG[A/G]ATTTCTTGCTTTTAA | 18519 |
rs108177940 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53634209 | ACCAACCAACCAAAC[A/C]AAACCAAACCCAAAT | 18519 |
rs108178018 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53585855 | TGAACTCAGGACCTT[C/T]GGAAGAGCAGTCAGT | 18519 |
rs108178268 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53577916 | TAGAATAACAGACTG[A/G]ATTCTATGACGAGGT | 18519 |
rs108180656 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53635996 | CATAATAACACCAAC[G/T]CGCTTCTCCCCAAGG | 18519 |
rs108181069 | snp | C/G | | | intron-variant | Kat2b | GRCm38.p3 | 17:53619464 | TCCTTCCCCTTCCCT[C/G]TCCTCCCCCTCCCTC | 18519 |
rs108182421 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53600139 | CTTGTTCGCTTGCTT[C/G]TTCTCTTGGGACACG | 18519 |
rs108185673 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53629511 | CTGGAACCAGTTAGC[C/T]ATCATATACCATTAA | 18519 |
rs108185743 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53637306 | TATATAGCTTGCTTA[C/T]TTATTTATTTATTTA | 18519 |
rs108186739 | snp | C/T | | | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53582987 | GTAAACCCAAAGCCC[C/T]GCCCCCCTTCCTCTC | 18519 |
rs108189606 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53633641 | TCATCAAGAAAAAAA[A/G]GGACAAAAGAGAAAG | 18519 |
rs108190857 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53640945 | CTTTCCTACCCAGAA[A/G]CCATCTTTTGAGCCT | 18519 |
rs108193747 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53593045 | AAACTGGCTGCTCTT[A/G]CAGAGGACCTAAGTT | 18519 |
rs108195916 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53631409 | AGTACCTGATTTCAG[C/T]TGTTGTGATAAAATA | 18519 |
rs108197170 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53640952 | ACCCAGAAGCCATCT[G/T]TTGAGCCTACTCCCA | 18519 |
rs108200341 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53575047 | ATTACATTGGTACTT[A/C]TCCTGATCACAAACA | 18519 |
rs108200905 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53592677 | GACTAACGGGGAGAG[A/G]CGTTGTGAGTTCTTG | 18519 |
rs108201742 | snp | C/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53598121 | CCTCCTCCTCCTCCT[C/T]CTTCTTCTTTTTATT | 18519 |
rs108202983 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53596011 | CAAGGTGAAGAAGGG[A/G]AGATAGAGATGCAGG | 18519 |
rs108204507 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53574988 | TGCTTTAGGCTTACC[A/C]TGGAAAACCTAATGG | 18519 |
rs108204547 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53578386 | TGTGTGTGTGTGTGT[C/G]TGGTGTACATGAGCT | 18519 |
rs108205488 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53586292 | TTGTCGTTGGTTGTT[A/G]CTGAGAACAGGGTCA | 18519 |
rs108208476 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53622406 | ACTGATAAGCAACTC[A/G]TTAAGTCCTAAAGAA | 18519 |
rs108209611 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53647985 | ATGCATGCAGGCAAA[A/G]TAGCAATGTATACAA | 18519 |
rs108210578 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53622119 | TGGCTTGACTCAAAC[A/G]ACCCACATCTCTCTG | 18519 |
rs108211566 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53642851 | ACTTCGAGATTCAGA[A/G]CCCTGTATGCTCGGA | 18519 |
rs108212003 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53611680 | GTTCTCCTAACACTA[C/T]TTTTTTTTTTTTTCG | 18519 |
rs108212010 | snp | C/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53619558 | GGTAGCCCTGGTTGT[C/T]TTGGAACTCATTATG | 18519 |
rs108212298 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53664072 | ATGTGTACTAAGTAG[C/T]GTGGAAACTCTAGAT | 18519 |
rs108213065 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53631988 | TCAGAGATCCATCTG[C/T]CTCTGCCTTCCAAGT | 18519 |
rs108214295 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53568707 | CACCTGCTGTGCCTT[C/T]CTGAGAGGGCTCCAG | 18519 |
rs108217103 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53623508 | AGCAGCAAACCTCAG[A/T]CGCTGGAGTACCAAT | 18519 |
rs108220756 | snp | A/C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53616618 | AGACACCACGGGGCC[A/C/G]GGGGGCTTTTAGTCT | 18519 |
rs108221571 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53600057 | AGGCTGTCTTTGAAC[G/T]CACAGAGACCCACCT | 18519 |
rs108221640 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53649811 | TCTCTGTCTCTCTCC[A/T]TCCTCCCTCCCTGCC | 18519 |
rs108222436 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53626369 | CTTGTAAAGATGTTA[A/G]GAAACACATCAAAAC | 18519 |
rs108225197 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53593265 | TAGGTAGGTAGGTAG[A/G]TAGATAGATAGATAG | 18519 |
rs108225401 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53642183 | GGGACATTTCATACT[C/T]AAACTGCAGTAACAG | 18519 |
rs108225528 | snp | C/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53643485 | CAAACACACACACAC[C/T]CCTCCTCATACTGCT | 18519 |
rs108225759 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53586708 | TTTTTTGTTTAGGAG[C/T]CAGCTATTCTTCTGT | 18519 |
rs108227027 | snp | A/G | | | upstream-variant-2KB | Kat2b | Mm_Celera | 17:53565131 | GAGCATAAGCATACC[A/G]CCCCTGGCCCTCGGG | 18519 |
rs108228127 | snp | C/T | | | upstream-variant-2KB | Kat2b | Mm_Celera | 17:53566645 | CATTTCGCCGACATG[C/T]AATGTTCTCAAACGA | 18519 |
rs108232284 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53632071 | TTGATTCTAAACTAG[G/T]AAGACTTCTTGATCT | 18519 |
rs108235207 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53636156 | AGCTTTTTCCTTCTC[G/T]TCTACCCATCTTCTT | 18519 |
rs108235344 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53599865 | TCTTTGCTTCCATTT[A/T]CCTTCTCTCTATTAA | 18519 |
rs108237801 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53601473 | TCTTATCTTGAGGGA[A/G]CCTTACTACTAAACT | 18519 |
rs108239709 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53598649 | GCCTCTCCTCTTTCC[C/T]TTTGTGTTCGTCATT | 18519 |
rs108240837 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53647451 | ACCAAAAAAAAAAAA[A/G]AAAAAAAAAAAGGAA | 18519 |
rs108241074 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53638943 | AACCAAGCAGCATCA[A/G]GACAATACCCATTCA | 18519 |
rs108242033 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53595620 | TTTTTTTTAATGTTT[A/G]TTTATTTCCTCCTTG | 18519 |
rs108243993 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53632441 | TTGAGAAATTATCTT[A/T]TTTTTTTTTTCTAAT | 18519 |
rs108245865 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53594195 | TTATTCACCACTTAT[C/T]GCTTCTGACTTTTGG | 18519 |
rs108246387 | snp | A/C | | | intron-variant | Kat2b | GRCm38.p3 | 17:53595043 | CTTCAACTTCTTGAA[A/C]TTCTCTTCTTCTTCC | 18519 |
rs108247399 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53632939 | GGGGGTTGTAGAAAC[A/T]GGCTTGTAGGGATCG | 18519 |
rs108247773 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53647397 | ACAGAGTGAGTTCCA[A/G]GACAGCCAGGGCTAC | 18519 |
rs108249402 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53626443 | TTCCTCTTTTTTTTT[C/T]TTTGTTGTTGTTGTT | 18519 |
rs108250018 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53576763 | CCATGAAAGCAGTTA[C/T]AGTAGCGGTGGTGGC | 18519 |
rs108251073 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53655499 | TGTTGGTGACCCCCA[A/C]ACAGAAAATTATTTT | 18519 |
rs108251210 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53642447 | TGCTTAGTTCTTTGA[A/T]GAAAGGTCTCTGGAA | 18519 |
rs108251544 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53601413 | GAGTCTCTCATATAC[C/T]AGGCAAGTGCTCTAC | 18519 |
rs108255167 | snp | A/T | | | downstream-variant-500B | Kat2b | Mm_Celera | 17:53673066 | CACATAATTAAAAAT[A/T]AGATAAAATCCAGTC | 18519 |
rs108255555 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53592239 | AGTGCTCATAACCTC[C/T]GAACCATCTCTTCAT | 18519 |
rs108259867 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53637107 | AACTTACATGATCCT[C/T]CTCTCTTGGCCACCT | 18519 |
rs108261649 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53636066 | GGTAGCAGTTTTGCC[A/G]TGAGTTCAAAGCCAG | 18519 |
rs108261722 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53637142 | ACTGCAATCACAGGG[A/G]TATGCCATCATGCCT | 18519 |
rs108262773 | snp | A/G | | | intron-variant | Kat2b | GRCm38.p3 | 17:53619795 | GCTGGGATTAAAGGC[A/G]TGCGCCACCACTGCC | 18519 |
rs108263136 | snp | C/T | | | upstream-variant-2KB, intron-variant | Kat2b | Mm_Celera | 17:53582907 | CAGGAGGGTAAGGAA[C/T]GGAGAGTTTAATTTG | 18519 |
rs108263344 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53624110 | TGAACCTGGGTCATC[A/G]GGCTTGTGTGGCCAG | 18519 |
rs108265555 | snp | A/G/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53621583 | TCAGAATTAGACTTC[A/G/T]TATAAGTAGAACAAT | 18519 |
rs108266013 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53568948 | GGCGTGCAAAAAAAA[A/T]AAATTGGAAGTATGT | 18519 |
rs108267129 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53654167 | CTCTCCCTCCAACCC[C/G]TATAGCCCGCTGGAC | 18519 |
rs108267243 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53576474 | TTATTATTATTATTA[A/T]TTATTATTATTATTA | 18519 |
rs108268600 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53586498 | AACGGCATAGAGAAA[A/G]CCAGTTTCAGAAAGT | 18519 |
rs108271079 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53599172 | GTTACAGTGAAAGAA[C/T]TAGAACTTAAATTTT | 18519 |
rs108271460 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53569820 | TGGAGCCTTTTTGGG[A/G]TGTAGGGCACGGGAC | 18519 |
rs108271868 | snp | A/C | | | intron-variant | Kat2b | GRCm38.p3 | 17:53597808 | CAAACAACCCCCCCC[A/C]CCCCCAGCTTCTGTG | 18519 |
rs108273149 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53601958 | TGTGTGTGTGTGTGT[G/T]TGTGTGCTTGTTTGA | 18519 |
rs108274461 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53611270 | GGTGGAGGGGGCGCC[A/C]TAGGGCTTTGGTGTT | 18519 |
rs108276712 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53575165 | AGCTTTTATAAGATT[A/G]GGATTTTAGGGGCCA | 18519 |
rs108277560 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53567653 | TCCCCCACCCACTCC[C/T]AGCTTCCCGCCGGCA | 18519 |
rs108277586 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53632334 | AATTCTGATTTTTTT[C/T]ATTTTGTAACTTCTT | 18519 |
rs108277958 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53633584 | TACAGGTGTGTACCA[A/C]CAATCCTGTGCTTGT | 18519 |
rs108278866 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53581781 | GCCCTGGCTGTCCTG[A/G]AACTCACTCTGTAGA | 18519 |
rs108279638 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53617762 | TAGAGGGTTAGACTC[C/T]ATGATAAAGGAGCAA | 18519 |
rs108279701 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53595202 | ATCCTAACTTCTTTT[A/T]GTTTTTTTTTTTTTT | 18519 |
rs108283105 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53639229 | TCCTGGAACTCACTC[A/G]GTAGGCTAGACTGGC | 18519 |
rs108283130 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53590567 | TTAGATATGTAGTGA[C/T]TGGTAGTGACTGGGT | 18519 |
rs108286754 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53635610 | CTACCTACCTACCTA[C/T]CTACCTACCTACCTA | 18519 |
rs108288641 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53599660 | CATGCACTACAATGT[A/C]TCTAGAGTCTAGATA | 18519 |
rs108288816 | snp | A/C/T | | | intron-variant | Kat2b | GRCm38.p3 | 17:53627762 | GGAAAGATATATTTG[A/C/T]TTCTCAAGTCAGAAT | 18519 |
rs108289985 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53623989 | CTGAGCCAGCTCACT[A/G]TCAGCCCCCGTACAC | 18519 |
rs108292965 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53591425 | GGAAGTTTCTCTGAC[C/T]CCTGCTAAGAACAGC | 18519 |
rs108297592 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53611587 | CAGATGGTTGTAAGC[A/T]TCCATGTGGTGCTGG | 18519 |
rs108301260 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53572453 | GGTCAACAAACCAAC[A/C]AACAAACAGCAACCC | 18519 |
rs108301877 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53667853 | AACCAGGCCAGAAGA[A/G]GACACTAGATCCCCT | 18519 |
rs108302286 | snp | A/C | | | intron-variant | Kat2b | Mm_Celera | 17:53614968 | GTTTTCTCCTAGCAG[A/C]CTTTAGGTGAAGATG | 18519 |
rs108302805 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53598591 | ATGTGGCCAAAGGAA[C/T]AACACCATGTTTCCC | 18519 |
rs108302856 | snp | C/G | | | intron-variant | Kat2b | Mm_Celera | 17:53637948 | CTCAAATTATACTCT[C/G]TACCTTACTCGTGCT | 18519 |
rs108303246 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53589869 | TTGGCAGAGGCAGGC[A/G]GATTTCTGAGTTCGA | 18519 |
rs108307281 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53588897 | TTTCTTTCTTTCTTC[C/T]TTTTTTTTTTTTTTT | 18519 |
rs108307805 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53599349 | AGATGACCTTTGAGA[A/G]TCTCGCTCTCCAACA | 18519 |
rs108309118 | snp | A/C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53634079 | GCCTGAATGAGTTTC[A/C/T]GGACAGCCAGAACTA | 18519 |
rs108309763 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53625466 | ATAGATTTCTTTCCG[C/T]CCACCAAACGGGTGC | 18519 |
rs108309805 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53577715 | ACGTAGACCAGGTTG[G/T]CCATAACCTTACAAA | 18519 |
rs108314251 | snp | A/T | | | intron-variant | Kat2b | Mm_Celera | 17:53635664 | ATCTATCTATCTATC[A/T]ATCATCCATCTATAG | 18519 |
rs108318826 | snp | G/T | | | intron-variant | Kat2b | Mm_Celera | 17:53584732 | TTAACTGGCTTCTAC[G/T]TCTTTAATTACATAT | 18519 |
rs108318970 | snp | A/G | | | intron-variant | Kat2b | Mm_Celera | 17:53601999 | CTCTTTGTAGCCCTG[A/G]GACATGCTGTATAGA | 18519 |
rs108319573 | snp | C/T | | | intron-variant | Kat2b | Mm_Celera | 17:53622405 | CACTGATAAGCAACT[C/T]ATTAAGTCCTAAAGA | 18519 |