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 |