SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3695859 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Btbd11 | Mm_Celera | 10:85408289 | ATCTCGTGATGTATT[C/T]CCCCAGATTTGAACT | 74007 |
rs3709139 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Btbd11 | Mm_Celera | 10:85405375 | GAGACATTGAGGTCT[A/T]CATGAACCCTCACCT | 74007 |
rs6162420 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85428461 | CCCTCCCGAATTCAG[A/G]AATAGATGAATCATT | 74007 |
rs6163532 | snp | A/C | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85428713 | tgcgcatgcaagtaa[A/C]acacccatagacaat | 74007 |
rs6164008 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85428791 | GGGGTTTTCCCCTCA[A/G]AATCAGGATACATTA | 74007 |
rs6177257 | snp | G/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85428871 | TGGAGCTGAGTGTTA[G/T]CNTAGGCATTTTGCC | 74007 |
rs6177258 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85428873 | GAGCTGAGTGTTANC[C/T]TAGGCATTTTGCCTG | 74007 |
rs6177327 | snp | A/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85428914 | TTTTTACTGTCCTAA[A/T]AACagatagacactg | 74007 |
rs6177757 | snp | A/G/T | 0.5 | 0 | intron-variant | Btbd11 | GRCm38.p3 | 10:85428965 | gtgaggaactgaggc[A/G/T]ttgagaatggtctcc | 74007 |
rs6177802 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85428984 | agaatggtctcctgc[C/T]cccaaatccccaagc | 74007 |
rs6177851 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85429016 | aggaggtgaagaagt[C/T]gggctttcagttcca | 74007 |
rs6179296 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85494890 | ATATAGGGAGTGGGG[C/T]GTGCTTGGTCAGAGT | 74007 |
rs6179822 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85494991 | AATGATAGTGAGGAA[C/T]NAGGGGAACAACTTC | 74007 |
rs6179823 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85494992 | ATGATAGTGAGGAAN[A/G]AGGGGAACAACTTCC | 74007 |
rs6180377 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Btbd11 | Mm_Celera | 10:85495105 | ACAGGGAAATGTACA[A/G]CGGGAAGAACAAGCT | 74007 |
rs6180967 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85495219 | ATCAGAATTTATGAT[A/G]CACAGGATGGAGCAA | 74007 |
rs6181424 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Btbd11 | Mm_Celera | 10:85495252 | AAAGGTACCCATTTA[G/T]AGACCACAGACTGCT | 74007 |
rs6193905 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85534939 | aagggttatatagtt[C/T]tggggaagtgggtag | 74007 |
rs6194413 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85535024 | ggaggcattccagga[A/G]tttcaggtgccggct | 74007 |
rs6194499 | snp | A/C | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85535070 | tggaaaaaaaggaag[A/C]ngaatctgtctgtca | 74007 |
rs6194501 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85535071 | ggaaaaaaaggaagn[C/T]gaatctgtctgtcat | 74007 |
rs6195990 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85535320 | TAGCATGCATGAACA[C/T]TTTCTTCATGGTGTT | 74007 |
rs6196071 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Btbd11 | Mm_Celera | 10:85535364 | CATGCATTGTCTTCT[A/G]TATGCTCCTTAGATG | 74007 |
rs6240260 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85590179 | cctggcatataacaa[A/G]ccctAGTTAATAGCT | 74007 |
rs6241369 | snp | A/T | 0.486111 | 0.0821678 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85590401 | GAACACCAGGTTTAG[A/T]GGCATGGTGGGATCC | 74007 |
rs6241819 | snp | G/T | 0.408163 | 0.193609 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85590449 | TGCCTCTAGCAAACT[G/T]TCTTTGATCATCCTT | 74007 |
rs6272553 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85630703 | CTATTTCTGTTGCCC[C/T]CTGAGGCTTGTGACA | 74007 |
rs6273597 | snp | A/C/T | 0.5 | 0 | intron-variant | Btbd11 | GRCm38.p3 | 10:85630851 | GTCCAGGCTGGGGTC[A/C/T]GAGACGCAGCCGCTT | 74007 |
rs6274770 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Btbd11 | Mm_Celera | 10:85631061 | GCATGCTGTTCAAGC[A/G]TCTCAGTGGTCACTC | 74007 |
rs6285226 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Btbd11 | Mm_Celera | 10:85473912 | GTCAACGATGATTCT[A/T]AGCTTTATACCCTCC | 74007 |
rs6285661 | snp | A/G/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85473942 | CTCTTCTGTGGCCCC[A/G/T]NGTTGAGGTTCCTTG | 74007 |
rs6285662 | snp | C/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85473943 | TCTTCTGTGGCCCCN[C/G]GTTGAGGTTCCTTGC | 74007 |
rs6285779 | snp | A/T | 0.304688 | 0.243945 | intron-variant | Btbd11 | Mm_Celera | 10:85474010 | CGACAGCTCTTTGAG[A/T]CTCTGGCAGTTCAGA | 74007 |
rs6286203 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85474028 | CTGGCAGTTCAGACC[C/T]GAGGTCTGNTGTGGT | 74007 |
rs6286220 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Btbd11 | Mm_Celera | 10:85474037 | CAGACCNGAGGTCTG[C/G]TGTGGTGTCTGCTCA | 74007 |
rs6286772 | snp | A/C | 0.207612 | 0.24638 | intron-variant | Btbd11 | Mm_Celera | 10:85474177 | GCTGAAAATTGGAAA[A/C]GCCTGTGGTCAGAAA | 74007 |
rs6286819 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Btbd11 | Mm_Celera | 10:85474208 | TTCACAGTAGATAGA[G/T]GCAGCCTACAGAAAT | 74007 |
rs6287335 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85474281 | GCACCAGGGGCAGCG[C/T]GCCTGNNCAGGGGGA | 74007 |
rs6287351 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85474287 | GGGGCAGCGCGCCTG[A/G]GCAGGGGGATGCCCT | 74007 |
rs6287352 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85474288 | GGGCAGCGCGCCTGG[C/G]CAGGGGGATGCCCTT | 74007 |
rs6385116 | snp | A/C | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85524733 | tgagccaaaagaaac[A/C]cttcctctctcaaat | 74007 |
rs13480682 | snp | A/G | 0.282481 | 0.247881 | intron-variant | Btbd11 | Mm_Celera | 10:85540810 | CTCTTCCAAGGCTCC[A/G]TCCCTCCCGTTCGCT | 74007 |
rs13480683 | snp | C/T | 0.484056 | 0.0878506 | intron-variant | Btbd11 | Mm_Celera | 10:85647373 | CCTCCTCCTCTGGAG[C/T]AAAGCTTGAACAATA | 74007 |
rs29310058 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85424909 | CCCACTGTGGGTGGC[A/G]ACATTCTCTAGAACC | 74007 |
rs29310459 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85546277 | ACATAATGATTGGGG[A/C]CAGCACCAATGGGAG | 74007 |
rs29311128 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85390504 | GCTCCTCCCATAGCT[A/C]TGTTAGTAGCTAATC | 74007 |
rs29311365 | snp | C/T | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | GRCm38.p3 | 10:85592232 | GCACAGTAGGACTGT[C/T]GCCATAGTAACCAAC | 74007 |
rs29312849 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85645174 | CCTGCCTCTGCCGCC[C/T]GAGTACTGGGATTAA | 74007 |
rs29313499 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85395351 | CTCCCTCTGTTGTTA[C/T]TTGTGTCCTCAAGCC | 74007 |
rs29313958 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85465934 | ACTCAGGAGACAGAG[G/T]CAGGGGCTGCAGGGG | 74007 |
rs29313998 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85410275 | ATGATTCTGTGTGTA[A/G]AGTGCTTGCCATGTT | 74007 |
rs29314305 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Btbd11 | Mm_Celera | 10:85560540 | AGCTTCATGGTAGGG[C/T]GTGCCTAAGAGAGTA | 74007 |
rs29314628 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85391510 | GCTTGTTTGAACACA[A/G]ATGGTCTACTTCAGT | 74007 |
rs29314656 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Btbd11 | Mm_Celera | 10:85559171 | TTATCATGTGCTGGG[G/T]TTTTTTTAAAGACGC | 74007 |
rs29314722 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85602209 | CAGGAATTACTAACT[C/T]CCTTTTGCAGGTAAC | 74007 |
rs29314924 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85457478 | TCAGAAGCCACTGGG[A/G]GACCGTCCACAACCT | 74007 |
rs29315283 | snp | C/T | 0.188366 | 0.242283 | synonymous-codon | Btbd11 | Mm_Celera | 10:85624993 | CTTCCGGATGCTGAA[C/T]TGTGGACGGACCGAC | 74007 |
rs29315331 | snp | A/T | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85453719 | CCATGCATGACTAAC[A/T]TAAGTTTCTTTTGCT | 74007 |
rs29315545 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85400585 | TCATCACTCCCAAGC[G/T]CTATAAAGGATCTTA | 74007 |
rs29315683 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85488321 | TTCAGTCCCTAATGA[C/T]CAAGCTTTCAAATCT | 74007 |
rs29315786 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85485854 | GGAAATGGAGGAAGA[A/G]TGGATTTGGAGGAGA | 74007 |
rs29315956 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85410053 | TCCCTTGGGGCAGTA[A/G]TTCCCCTTCCATGAC | 74007 |
rs29316531 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Btbd11 | Mm_Celera | 10:85608802 | GCAGAGTGGAAACAC[A/G]TTTGGTGCTCACAGC | 74007 |
rs29316591 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85641169 | CAAAGAAGAATGGGA[C/G]AGGGGGAAGGGGCTA | 74007 |
rs29316810 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Btbd11, LOC105245252 | Mm_Celera | 10:85594108 | TTTTAAGACCCTCAT[C/T]CTAGCTGCCTAGAAG | 74007 |
rs29316830 | snp | A/C | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85400841 | TTCTGAGCTTGGAAC[A/C]CTTTGACGGAAGAGA | 74007 |
rs29317004 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85600307 | CTGTGGTCCAGGCTC[C/T]CCTTGCTACAGGAGT | 74007 |
rs29317063 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Btbd11 | Mm_Celera | 10:85448918 | TGGGTTGAGTCCAAA[C/T]GCAGGGAGGAAGCCT | 74007 |
rs29317386 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | Btbd11 | Mm_Celera | 10:85401377 | GTCTGGTCAGATAGT[C/G]TGGACACTGTTCTTT | 74007 |
rs29317504 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85468984 | GTCACCCACCTGCTT[C/T]TCAGCTCTGTGCTAT | 74007 |
rs29317812 | snp | A/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85427201 | CACTGTCAAGAGATT[A/T]AAAAAGATTAACAAT | 74007 |
rs29317971 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85394290 | CTGAGTGATAGAAAT[C/G]TCCCACATGTTAATA | 74007 |
rs29318029 | snp | C/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85596174 | ATGAACAGATATTAA[C/G]GGCTTCCAACCTGCC | 74007 |
rs29318035 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85649709 | CAGCGATTTCAGCCC[A/G]TGGCTCGACCTTGAA | 74007 |
rs29318239 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85546754 | GCCAGTGAAATTAGG[A/G]AAGATGAGGGCTCTA | 74007 |
rs29318271 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85385591 | TCCTCCACACCCTTG[C/T]TGATGCTTGTAATCT | 74007 |
rs29318409 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Btbd11 | Mm_Celera | 10:85408862 | AGGTGCCCCGGGTCA[A/G]GACACAGTTGTGGTA | 74007 |
rs29318959 | snp | A/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85620805 | TACATGTACGCGTGC[A/T]CAGGCACACACAGAC | 74007 |
rs29318972 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Btbd11 | Mm_Celera | 10:85569908 | CACCCCATGCCAAAA[A/G]ATGTGCCAGATGTGC | 74007 |
rs29319031 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85652364 | GATCTCATTACGGAC[A/G]GTTGTGAGCCAACAT | 74007 |
rs29319419 | snp | C/T | 0.35503 | 0.226867 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85591568 | GGGGCTCAACAGGCT[C/T]CTCAGACAACAGGAA | 74007 |
rs29319738 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Btbd11 | Mm_Celera | 10:85626191 | GACTAGTCTTTGCAC[A/G]CCTCTAGTTATATAT | 74007 |
rs29320202 | snp | G/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85573589 | TCTTTCATCAGAACT[G/T]CTTAGCTCTTCTGAA | 74007 |
rs29320217 | snp | C/G | 0.188366 | 0.242283 | intron-variant | Btbd11 | Mm_Celera | 10:85502775 | GTCCGGGAACTCCAC[C/G]TCTCCAGGGCCAAAA | 74007 |
rs29320356 | snp | A/G | 0.290657 | 0.246672 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85578913 | GAGATTCTACAGGGA[A/G]CATTTTGCTTCTCAG | 74007 |
rs29320489 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Btbd11 | Mm_Celera | 10:85509577 | CCAGTTTTCTGCCTT[A/G]ACTGCAATACACAGG | 74007 |
rs29320530 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Btbd11 | Mm_Celera | 10:85510910 | TTATCAGCCTCAGCA[C/T]AATGCTGGTTACCAG | 74007 |
rs29320744 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Btbd11 | Mm_Celera | 10:85618277 | CCAGGTGGTGTGTGC[C/G]TGTAATCCCAGCACC | 74007 |
rs29320764 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Btbd11 | Mm_Celera | 10:85469491 | AGTCCTGCTGCCATG[C/T]TGTGAGAAAGCCTGA | 74007 |
rs29321217 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Btbd11 | Mm_Celera | 10:85643358 | GCCCTTCCTGAGAGC[A/G]TGAGTTCTGTTCCCA | 74007 |
rs29321679 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85645267 | CTCAGGTCAGCCCAC[A/G]TGCTCTGACAGAGCT | 74007 |
rs29321755 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Btbd11 | Mm_Celera | 10:85475816 | ACAGTAGAGCTGTAG[C/T]AGCTGAGAGCAGTGG | 74007 |
rs29321853 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Btbd11 | Mm_Celera | 10:85636018 | AATTTATTGAAGTAC[C/T]TTGGATTTATGTCTT | 74007 |
rs29322944 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Btbd11 | Mm_Celera | 10:85501678 | AGCTGTGTATGCAAA[A/G]CTGTAGCCTCTCCTC | 74007 |
rs29323193 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Btbd11 | Mm_Celera | 10:85456047 | TCTCCATCCTCCAGT[C/G]CATAGCTGCTCACAG | 74007 |
rs29323237 | snp | A/C | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85618748 | AGTGCTTACACAGGG[A/C]AGGACGTGTCTGCAA | 74007 |
rs29323295 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85391730 | ATCCTCCAAGCTGAA[A/G]GGCGTCCCTAACGCC | 74007 |
rs29323381 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85641159 | TCCCCCTTATCAAAG[A/G]AGAATGGGAGAGGGG | 74007 |
rs29323839 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85427576 | CAAGCTCCAACCATC[A/G]AGCTACCACGGGCCT | 74007 |
rs29324168 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85589174 | AGAAAAGCTGACGAG[A/G]CCTGGCCCCTCCTCT | 74007 |
rs29324307 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85386431 | GGGAGGAGAAACGTG[C/T]ATCTTGTATGGGCTG | 74007 |
rs29324456 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85385408 | AGGGAGAGGGGAGTA[A/G]ATAGATCTTTTAAAT | 74007 |
rs29324860 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Btbd11 | Mm_Celera | 10:85632754 | GACAAACGCCTCCTC[A/G]TTAAGACTTTTCCTC | 74007 |
rs29324872 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85611282 | TCTTTACTGGCTTGC[C/T]TCCCTTGGCTTGCTC | 74007 |
rs29325158 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Btbd11 | Mm_Celera | 10:85536060 | TTTATGATTGCTGTT[C/T]GCAAACGGTTTAGGT | 74007 |
rs29325301 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85428162 | AGAAAACCCTCACCA[A/G]ACCCCGAGTCTGCTG | 74007 |
rs29325329 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85574089 | CTCTCCTAGGTGTTA[C/T]TCCCTTTGCCATCCC | 74007 |
rs29325440 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Btbd11 | Mm_Celera | 10:85426838 | TGAGACTTTTATCAT[A/G]GGCTGTCTCGACTCT | 74007 |
rs29325493 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85499812 | GCTGGTGAGTCTCCC[A/G]CCTCTCAATTCTTCC | 74007 |
rs29325591 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85602467 | GGTTCAAACAATCCA[C/T]TTATTCTTTCTTAAT | 74007 |
rs29325614 | snp | A/C | 0.475309 | 0.108333 | intron-variant | Btbd11 | Mm_Celera | 10:85500129 | CTTGGCCAAAGAAAC[A/C]ACAAGGCCCAGCTCA | 74007 |
rs29325749 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85602247 | GAGAGTCGCTTTTGT[A/G]TGTTTGCTTGTTTTT | 74007 |
rs29325892 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Btbd11 | Mm_Celera | 10:85513567 | ACCTGAATACGTATG[C/T]ACACCCATCTGTGTA | 74007 |
rs29326004 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85437370 | CAGCTCCCTGGATGG[C/T]GGGGCTGAATCCAAA | 74007 |
rs29326146 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85395313 | GTTCTGATGGCCTCT[A/G]AAGTGGAAGAAAACT | 74007 |
rs29326636 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85635097 | GAGTCAGTAATCATG[C/T]GGACCTCTCTAGGCA | 74007 |
rs29326731 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85390515 | AGCTATGTTAGTAGC[C/T]AATCATTTTCCAAAT | 74007 |
rs29327379 | snp | A/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85573175 | TAACCCCAACAAAAA[A/T]ACCAGCTGAGGAGAG | 74007 |
rs29327398 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Btbd11 | Mm_Celera | 10:85488525 | TAGAAATTTTAATTA[A/C]TCAAACAGCTGTTGG | 74007 |
rs29327412 | snp | A/T | 0.401235 | 0.199068 | intron-variant | Btbd11 | Mm_Celera | 10:85503381 | GCTGGCCCAACAATA[A/T]AAGAAGTGGAGGGAA | 74007 |
rs29327552 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Btbd11 | Mm_Celera | 10:85625796 | GACTGTATAATGACA[A/G]CTAATCACTTTCTTG | 74007 |
rs29327638 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85454566 | GTCTTATTCGTAAAG[C/T]CCCTCCATTCACTTG | 74007 |
rs29328268 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85477630 | AATCCAGTTCCAAAG[C/T]CCTGGTCCTTGGGTG | 74007 |
rs29328284 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85385571 | ATAGAGTACACTCTT[C/T]TTTATCCTCCACACC | 74007 |
rs29328315 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85557734 | ACTGAAAAGCAGAAG[A/G]GTGTTCACAATCCAA | 74007 |
rs29328493 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Btbd11 | Mm_Celera | 10:85636504 | CCTAAAAAGAACGGC[A/G]CACCCAGGAGGAGGA | 74007 |
rs29328696 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Btbd11 | Mm_Celera | 10:85430371 | CCCTGCAGGGCTGGG[C/T]GATGTTACAGCCGTT | 74007 |
rs29329039 | snp | A/C | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85465814 | AAGTGCTGCCTTTTC[A/C]CAAGGGAACATTAGT | 74007 |
rs29329116 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85609793 | TTGTACGGCGAGGAC[C/T]TTTTTAAATGAGCTA | 74007 |
rs29329281 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85609698 | CCAGGAACACATTTG[C/T]CTTTACCTCCTAATG | 74007 |
rs29329325 | snp | C/T | 0.42 | 0.183303 | intron-variant | Btbd11 | Mm_Celera | 10:85647315 | GACAGCAAGTATGGG[C/T]GCAATGCTCTTGGGG | 74007 |
rs29329507 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Btbd11 | Mm_Celera | 10:85639785 | ATTCATCTAGCCCCT[A/G]TCTTAGCCAGTTGCC | 74007 |
rs29329906 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85455096 | CTTATCTTCTGTTCT[C/T]CTCCTTTTCCTCCTC | 74007 |
rs29329969 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85625325 | AAATCTCACATGATT[A/G]TCGCAGCTGAAATTT | 74007 |
rs29330394 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85452452 | GAGAGAGCCAGGGGA[C/T]GGGAGCTAACCATTG | 74007 |
rs29330552 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85560106 | CTCAGGGTTGAGGAG[C/T]ATGGATGGCTAAGTG | 74007 |
rs29330796 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Btbd11 | Mm_Celera | 10:85637088 | ATCAGACAGGGAACC[C/T]ATTTTTAACACGTTT | 74007 |
rs29330885 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Btbd11 | Mm_Celera | 10:85575080 | AGACAGACTACCTAA[C/T]GAACACTGGTGAGGG | 74007 |
rs29330943 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Btbd11 | Mm_Celera | 10:85517071 | TAATTTTTTGTCCAC[A/G]AATGGTAGTTGTTCC | 74007 |
rs29331027 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85386127 | ATTTAAGTCTGAGCA[A/G]TCTAGAGCATTGTCC | 74007 |
rs29331131 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Btbd11 | Mm_Celera | 10:85608425 | GAAAGGGAAGGAGGA[A/G]GACAGTCAACAGAGT | 74007 |
rs29331334 | snp | A/C | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | GRCm38.p3 | 10:85592193 | TCCTACAGGAACCAC[A/C]CCATTGGCAGACAGC | 74007 |
rs29331378 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85547925 | GATGACCCAAATTCT[A/G]TCCCCAAGCCCCACA | 74007 |
rs29331379 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85635078 | ATTTCCCTGTCTGTA[A/G]AATGAGTCAGTAATC | 74007 |
rs29331396 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Btbd11 | Mm_Celera | 10:85410692 | GAAAGGCAACAGGCC[C/T]GACTATTGAAAAGTG | 74007 |
rs29331676 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85609659 | CCTGGAGCCCACTGA[C/T]TTGGCTAGGTTTGGA | 74007 |
rs29331742 | snp | A/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85634985 | GTTTCCTGGAGCCAA[A/T]TTACAAGGGTTCAAA | 74007 |
rs29332044 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85386709 | ATGGAAGGGAGGAAT[A/T]AAAAAAAAAACTAAG | 74007 |
rs29332191 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85626617 | ACCCCTTCCTCCTGT[C/T]GGTTGTGATGAGCAG | 74007 |
rs29332297 | snp | C/G | 0.375 | 0.216506 | intron-variant | Btbd11 | GRCm38.p3 | 10:85447961 | ACACACACACACACA[C/G]ACACAGAGAGAGAGA | 74007 |
rs29332361 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Btbd11 | Mm_Celera | 10:85468384 | AAACCAGAGTGGATG[A/C]TAAACCTGGTAAGGC | 74007 |
rs29332440 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85460995 | GACCTGATTAGGGCA[A/G]TCGGAAACATCTCTG | 74007 |
rs29332527 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85599864 | ATAGATGAGTACCTA[C/T]GAAGTGCTTCCCAAG | 74007 |
rs29332556 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | GRCm38.p3 | 10:85427263 | TTTAAAAATTTTTTC[C/T]CCAAATAGCTTTATA | 74007 |
rs29332924 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85386508 | TCGGACAAACACTTT[A/G]TGAACCGCAGAGTGG | 74007 |
rs29333077 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85552455 | AGAAAATAGACAACA[A/G]GTCTTAGTTCAAACG | 74007 |
rs29333174 | snp | A/C | 0.42 | 0.183303 | intron-variant | Btbd11 | Mm_Celera | 10:85491125 | GCTACTTGTATTTTA[A/C]CTGCTCCCTCTGACC | 74007 |
rs29333393 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Btbd11 | Mm_Celera | 10:85577786 | TTCCTTTCCACAATC[A/G]CAGAGAGGATCTCTT | 74007 |
rs29333537 | snp | G/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85574770 | TCTAAAGATTTTGAT[G/T]CATGAATTTGGACCT | 74007 |
rs29333542 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85489208 | GATTTCAACCTATAG[A/G]GTTTGAAGAGGGGAT | 74007 |
rs29333732 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85505033 | CTGCCTCCTCCCCAT[A/T]TGTAGGACTAAGATG | 74007 |
rs29333819 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85560383 | CCTACACAAATGTGC[A/G]CATAAATCCATGTAC | 74007 |
rs29333873 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85449823 | AGTGGGTGGGTCCTT[A/G]AGATGGAGAAGACAT | 74007 |
rs29333995 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Btbd11 | Mm_Celera | 10:85447801 | ACTAGTGCATGGGCG[C/T]GCGCGCACACACACA | 74007 |
rs29334109 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85610386 | GTCAAAGCTGAATGT[A/G]GCAGTACACATCTAT | 74007 |
rs29334494 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Btbd11 | Mm_Celera | 10:85440527 | TGCCTCTTGTCCCCA[C/G]CTGAAGACTCGTGAC | 74007 |
rs29335186 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85410131 | GTGTGATGTCACTTT[C/T]ATCTTTGGCCAGAAG | 74007 |
rs29335409 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Btbd11 | Mm_Celera | 10:85410664 | GGGGACAGGGACACA[A/G]AAGGTTCTAGAAGAA | 74007 |
rs29335522 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Btbd11 | Mm_Celera | 10:85437111 | ATCTGAAAGGAGTGC[A/G]TGTAAGTAGTTCTGG | 74007 |
rs29335717 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85388965 | CGCTAGGAAGGCATG[A/G]CTGAGGGCAGCGAAG | 74007 |
rs29335728 | snp | A/C | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85645290 | ACAGAGCTGTTGCCC[A/C]GCTGAGCCATCTTGC | 74007 |
rs29335731 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Btbd11 | Mm_Celera | 10:85620541 | TATTTGCATCCAACT[C/T]TTGCTTCGCCTATTA | 74007 |
rs29335787 | snp | A/C | 0.42 | 0.183303 | intron-variant | Btbd11 | Mm_Celera | 10:85648359 | TACCAAAGCAGAAAT[A/C]CTGTTCCCTCTGCCT | 74007 |
rs29336045 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85395520 | GCACTCACAGCGCTC[A/G]TTGCAGATCAGGCAC | 74007 |
rs29336190 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85636471 | AACACAGGTAGCGCC[A/G]TTCTCTGAAGGCACA | 74007 |
rs29336547 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Btbd11 | Mm_Celera | 10:85597510 | TCTGTGTTTCAGCAA[A/G]CCATTCAGGGAGCTG | 74007 |
rs29336804 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85577711 | CCTTTACCCTACAAG[A/G]AGCCTGGCCCGGCCA | 74007 |
rs29336974 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85492972 | CAGCCCGTTGTTTGA[A/G]AAGCCCTCTGAGCTC | 74007 |
rs29336983 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85386571 | ATAGTTCGAAAGCAG[A/G]AACTAGGGAAGCTAC | 74007 |
rs29337104 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Btbd11 | Mm_Celera | 10:85469504 | TGCTGTGAGAAAGCC[C/T]GAGACCAGCAGGCTG | 74007 |
rs29337225 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85385772 | CGTCCTTCCCTTGTC[A/G]ACTCATACATTTACC | 74007 |
rs29337332 | snp | C/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85402878 | GTCGTGGCGACTCCC[C/G]CCACAGCATTACTTC | 74007 |
rs29337334 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85595319 | AGACAGACACACAGA[C/T]GCACGTGGGTGTGCA | 74007 |
rs29337588 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85454559 | ACCAGCCGTCTTATT[C/T]GTAAAGTCCCTCCAT | 74007 |
rs29337750 | snp | C/T | 0.5 | 0 | utr-variant-5-prime | Btbd11 | GRCm38.p3 | 10:85386892 | AACCGCGGCCCGGAT[C/T]CCGGAGCCGGGGGAG | 74007 |
rs29337926 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85461077 | AGATGCTTCCTAGTT[C/T]GCCAGATTTTGGATA | 74007 |
rs29338355 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Btbd11 | Mm_Celera | 10:85616838 | AACCCCTGCCGACTC[C/T]ACACTCCTTCTGGGA | 74007 |
rs29338403 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85399381 | TATATCTGAGAGCTC[A/G]TCAGGGTGGCTGCCA | 74007 |
rs29338485 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85641117 | TGACCTGATGTGCCA[C/G]GGTGGGTTGGTATGG | 74007 |
rs29338583 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Btbd11 | Mm_Celera | 10:85544825 | TCTGGCCTTCCCTGT[C/T]TGAAAACTGAAAGGT | 74007 |
rs29338627 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85573719 | AGAGCTGCATTTGTC[A/G]AGAGGAGGCAATGCT | 74007 |
rs29338760 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85546155 | TGCTTGCCTAGCAGG[A/G]ATGACTAGGCTTGAT | 74007 |
rs29339028 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85560398 | GCATAAATCCATGTA[C/T]GCACATGGTGACAAA | 74007 |
rs29339633 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85510968 | AGCTGGGTTTCACCA[A/G]CAACCTCTCCACCTC | 74007 |
rs29339946 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Btbd11 | Mm_Celera | 10:85406061 | TTGTTTTCATAATTT[A/G]CTAGAGCCCTGGCAT | 74007 |
rs29340029 | snp | G/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85636502 | GGCCTAAAAAGAACG[G/T]CGCACCCAGGAGGAG | 74007 |
rs29340151 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Btbd11 | Mm_Celera | 10:85640621 | TGGGTGAGCAGTGGT[C/T]CGGGTATACTCAGGC | 74007 |
rs29340247 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85430523 | GGCTTCTCATGGCTT[C/T]CAAAGATACTCACCC | 74007 |
rs29340435 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85608895 | CCAGATCTGGGCTGT[C/T]GGTTAGGAGGGTGAC | 74007 |
rs29340446 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85499930 | GGTGATGGAGAAGAG[C/T]GCTTACAAAATACGA | 74007 |
rs29340819 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85509441 | GTCAGGGAACTTTAG[C/T]AGCAGAAATAAAACA | 74007 |
rs29340916 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85386104 | AAAGAATATTCTCCT[C/G]TGCACAAATTTAAGT | 74007 |
rs29340922 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85595336 | CACGTGGGTGTGCAC[A/G]TGCACACATACACAT | 74007 |
rs29341083 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85400531 | GGATGGAGGGAATGT[A/G]CCCTCTGTAGGTCAC | 74007 |
rs29341490 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Btbd11 | Mm_Celera | 10:85388324 | AACCACAGCCACCGC[C/T]GCCGCCGCCGCCAAC | 74007 |
rs29341604 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85648393 | CGACACACTGGCATT[A/G]CCTACAGATCTTTGA | 74007 |
rs29342084 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85411112 | GACCTTACATTCTAT[A/G]ATGGAGACCTGCAGA | 74007 |
rs29342119 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85472833 | CCAGCCTTTTTGTGC[C/T]CAGTGTCATCAGATG | 74007 |
rs29342315 | snp | C/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85505741 | GGGTGCTGTTTTAGG[C/G]GAGGCAGAGAAGGAA | 74007 |
rs29342404 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85467868 | ACAACTGTGAGGGGA[C/T]TCACTTTTGGAGGTG | 74007 |
rs29342531 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Btbd11 | Mm_Celera | 10:85428314 | AGACTGCAGACTGTG[C/T]GGGAGCTGGCTAGTG | 74007 |
rs29343274 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85410078 | CATGACACTGGCTTA[A/G]AAGAGCCAGGATTGG | 74007 |
rs29343649 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85590328 | CAAGTTACAAAGAAT[C/T]CATGTGCCCAGAATT | 74007 |
rs29343668 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85578276 | GGTTCTGGCATGCCC[A/G]GGAATTTTGGCCAAG | 74007 |
rs29343808 | snp | A/C | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85655179 | TTATAGAGGGAAGGG[A/C]TAATTTGGGCTTCCA | 74007 |
rs29344107 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85390873 | CTAACATACACTGAA[A/C]ACCAAGCCTGTTCCT | 74007 |
rs29344322 | snp | C/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85574866 | GAGGCAGAGAAGAGC[C/G]GCAAGTGGCTCAAGG | 74007 |
rs29345127 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Btbd11 | Mm_Celera | 10:85595568 | CTTACAAACTGCCAG[A/C]GTCCAGTGATAGACA | 74007 |
rs29345288 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85577689 | GAAATTGGCTGAGAA[A/G]TCCAGCCCTTTACCC | 74007 |
rs29345345 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Btbd11 | Mm_Celera | 10:85510935 | TACCAGGTTCCCAGG[C/G]TAGCTGCTGCATTGC | 74007 |
rs29345813 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85617720 | CTGAGGTCACGTGTC[C/T]GAAGCGGCAGAAGAT | 74007 |
rs29345965 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85386056 | AGAAATGCAGCAGAC[A/T]CACACATATATTTTG | 74007 |
rs29346028 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85627531 | TCCTAGCTCCTGACT[C/T]ATCCTTTCTAGGATG | 74007 |
rs29346240 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85483096 | AGTCCCAATAAAATC[C/T]GTTTATGACTGAGAA | 74007 |
rs29346989 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85469379 | TTCTCTTCATCTATG[C/T]CTCCCTCCCTTTCTT | 74007 |
rs29347030 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85406015 | GGGCTCCGATGCTTG[A/G]GAGGGTGGAGGGGCG | 74007 |
rs29347521 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85501164 | CTTTCTGAACTTTCT[C/T]GTTCTGAAAGTTAGA | 74007 |
rs29347870 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85513505 | CAAAAATAAGGTGTC[C/G]GGCAACTTAAGGAGT | 74007 |
rs29348167 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Btbd11 | Mm_Celera | 10:85411213 | TCTTACTTTTCTGTG[A/G]CAAAAGCAGACAGTT | 74007 |
rs29348233 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85485888 | GAGGTGGGGAGGGGA[A/G]TGGTAGAAGTAGAGG | 74007 |
rs29348258 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Btbd11 | Mm_Celera | 10:85578003 | AAAAAGAGCATGTCT[A/G]CAGCTCCAGAAAACA | 74007 |
rs29348356 | snp | A/T | 0.487535 | 0.077957 | intron-variant | Btbd11 | Mm_Celera | 10:85510953 | GCTGCTGCATTGCTC[A/T]GCTGGGTTTCACCAG | 74007 |
rs29348581 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85510241 | TTGCATCGATTCCAT[C/T]TTAGCTGGATTTTTT | 74007 |
rs29349030 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85557615 | GGGATAGGCACTGAG[C/T]CGGGAACAGAAGTTA | 74007 |
rs29349339 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85454420 | AAGGACTCCATGATG[A/G]CAATACAGGCAGGTT | 74007 |
rs29349509 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85582687 | CAACCATCTATTGAA[C/T]GCTCAAGTCTCTTTC | 74007 |
rs29349605 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Btbd11 | Mm_Celera | 10:85578096 | CATGCGCTTGGCTCC[A/G]CCTTCTTGGTGCATA | 74007 |
rs29349682 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85573404 | ACCCATAATGGACTG[A/G]ATGCTTCAGCATCAG | 74007 |
rs29349853 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85585009 | GGACAACAACTCTGT[C/T]CCCCAGGACTGGGGC | 74007 |
rs29350033 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85586794 | AGCGCCATCATCATT[A/T]CCCTCTGCTTATCCC | 74007 |
rs29350122 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Btbd11 | Mm_Celera | 10:85394839 | TCCCCAGTCATTTTA[C/T]AGACATTAATTAACG | 74007 |
rs29350418 | snp | A/G | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85592697 | TGTCAGCAACACCCT[A/G]TGTTTGTTCCCTGAG | 74007 |
rs29350700 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85619043 | AAACATTTCATTGGA[A/G]TTGGCTTACAGTTTC | 74007 |
rs29351085 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Btbd11 | Mm_Celera | 10:85629793 | TGAGTCTTGACTCTC[A/G]AGAATCGGCTCCCGG | 74007 |
rs29351446 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85612161 | TAAGAGTATTGGCTG[C/T]GTTTCCAGAGGACCC | 74007 |
rs29351628 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Btbd11 | Mm_Celera | 10:85402667 | ACCTTTAAATGCTCT[G/T]ATGCTGAGACAGGAG | 74007 |
rs29351819 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85388932 | CTTGCCCCAGGCCCT[C/T]TGGGGTCGCTGTGGA | 74007 |
rs29351893 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Btbd11 | Mm_Celera | 10:85609909 | TTCTTCATTCCCTAG[C/T]CCTTTGAGTAGCCTG | 74007 |
rs29351897 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85410069 | TTCCCCTTCCATGAC[A/G]CTGGCTTAGAAGAGC | 74007 |
rs29352271 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Btbd11 | Mm_Celera | 10:85475965 | CTCTAAGGCTTGGAT[A/G]CACAGGTGGAGATTG | 74007 |
rs29352338 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Btbd11 | Mm_Celera | 10:85544893 | TGTCTGCCAGGCTGC[A/G]ATGTTTCCCAAGCTC | 74007 |
rs29352900 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85406161 | ATCTCCTTTCCAACG[C/T]CCCACCCTGCTGCTA | 74007 |
rs29353332 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85385323 | ATTTGTTATACATGG[C/T]AAGATTTCCTTCTTT | 74007 |
rs29353678 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85515895 | AGGGGAGGCAGGACG[A/G]GGCTAGACTTGAATG | 74007 |
rs29354252 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85635061 | CTAAACTCTCTGCCT[C/T]AATTTCCCTGTCTGT | 74007 |
rs29354415 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85482146 | TATTTGCATTCCAGC[A/G]CAGCCCCATTGCCTC | 74007 |
rs29355030 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Btbd11 | Mm_Celera | 10:85638858 | TATCATCCGCACCAT[C/T]CTTGAGAAGAACCCC | 74007 |
rs29355203 | snp | A/C | 0.188366 | 0.242283 | intron-variant | Btbd11 | Mm_Celera | 10:85609088 | TAGTTCTACAGGATC[A/C]GTATCTGCCCCTAGG | 74007 |
rs29355664 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Btbd11 | Mm_Celera | 10:85401267 | TCCCAGACCCTGATG[C/T]AAGCACACAGGGACT | 74007 |
rs29355985 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85428083 | TGGCTGGAGGAGACC[C/T]CAAGAGAACCTTGCC | 74007 |
rs29356053 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85473767 | CTTCGTTTATGGATG[A/G]CCTTCCTCCTCCAGC | 74007 |
rs29356362 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85386497 | GAAAGTAACCCTCGG[A/G]CAAACACTTTATGAA | 74007 |
rs29356667 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Btbd11 | Mm_Celera | 10:85604573 | CTTTCTTCTTAGGTC[A/G]TCAACAGAGCCTGTG | 74007 |
rs29357105 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85591402 | TTTAAATGTTAATTT[C/T]AGCAACAACAAAAAG | 74007 |
rs29357157 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Btbd11 | Mm_Celera | 10:85625702 | CAGTGTGAATCCTGA[A/G]TGCTGTTACAAGGGA | 74007 |
rs29357238 | snp | C/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85447665 | AAATTATGAAAGGTT[C/G]AGAGCGCTCATTTCA | 74007 |
rs29357241 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85635170 | CCCACTATAACACCA[C/T]ATAAAAGCTTTCTTA | 74007 |
rs29357592 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85453981 | GGCTGGGCCCTCCCC[C/T]ATTGATCACTAATTG | 74007 |
rs29357610 | snp | A/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85395252 | TAGTAATAATGACCC[A/T]ATAAGCCAGGGAAGG | 74007 |
rs29357695 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85609574 | GGTGCCCTTCCTCCA[C/T]CATTCTGCTGCTCTT | 74007 |
rs29357711 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Btbd11 | Mm_Celera | 10:85461659 | TGACTATGTGAGAAG[A/C]AAACACACATATCTC | 74007 |
rs29357788 | snp | G/T | 0.304688 | 0.243945 | intron-variant | Btbd11 | Mm_Celera | 10:85595444 | AGGCCCTAAATTTCT[G/T]TCCTATCACTAACTC | 74007 |
rs29357893 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85560541 | GCTTCATGGTAGGGT[A/G]TGCCTAAGAGAGTAA | 74007 |
rs29358015 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85578026 | AGAAAACAAGCAAGA[A/G]TGTTGGCCTTGGTTT | 74007 |
rs29358089 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Btbd11 | Mm_Celera | 10:85648100 | GCGTGTACTATAACA[A/G]CTCAGGCCCAGGATG | 74007 |
rs29358126 | snp | C/G | 0.42 | 0.183303 | intron-variant | Btbd11 | Mm_Celera | 10:85646065 | TTCCACAGCAGCCTC[C/G]AGGGGCCCACTCTCC | 74007 |
rs29358412 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85385324 | TTTGTTATACATGGC[A/G]AGATTTCCTTCTTTT | 74007 |
rs29359038 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85455950 | CCCCTGCCCCCCCAC[C/G]CCCCCTTGCCCCAAG | 74007 |
rs29359407 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Btbd11 | Mm_Celera | 10:85515508 | CCAGAGGTTCCCAGG[A/G]GAAGACAGTGTTCAG | 74007 |
rs29359574 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Btbd11 | Mm_Celera | 10:85609982 | AACTTGCCTGACACT[A/G]TAACCCTTGTGGGAT | 74007 |
rs29359931 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85550583 | GCGTGCTGCAGAAAT[C/T]GTTTTTAAGGATAAT | 74007 |
rs29360346 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Btbd11 | Mm_Celera | 10:85608860 | GAGTGGCATTTGGTG[C/T]CTGTTCCCGGACTAG | 74007 |
rs29360720 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85410270 | GGGAGATGATTCTGT[G/T]TGTAGAGTGCTTGCC | 74007 |
rs29361401 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Btbd11 | Mm_Celera | 10:85424767 | CTCATGACCCGATAA[A/G]TCTGAAAATCCTGGA | 74007 |
rs29361475 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85452384 | AATCTCGCCCAGCAG[A/G]TGTCCATCTGTGGGG | 74007 |
rs29361587 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Btbd11 | Mm_Celera | 10:85602822 | GTCTGGCACTCATTT[A/G]CCATTGTTCTTCAGA | 74007 |
rs29361692 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85503668 | CCGCTCTGCTCTGTG[C/T]GGCGCGGCAAGTCTT | 74007 |
rs29361818 | snp | A/T | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85489917 | TCTGGTTTCTTAATT[A/T]TGCAGTGAAAAGGTG | 74007 |
rs29361859 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85410077 | CCATGACACTGGCTT[A/C]GAAGAGCCAGGATTG | 74007 |
rs29361904 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85643399 | CAGACAGCTCACAAC[C/T]GCCTGTAAGTCCAGA | 74007 |
rs29361933 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Btbd11 | Mm_Celera | 10:85544793 | GGGTCTCTTGCATAG[C/T]GGGCACCTTCTGTAG | 74007 |
rs29361987 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85560158 | CCCAGGTTCAAACCC[C/T]CACTCTCCTCCTCTT | 74007 |
rs29362078 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85459579 | TTTTTTCAATTATGA[A/G]TTTAAGAGCTAAGCT | 74007 |
rs29362322 | snp | A/G | 0.21875 | 0.248039 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85592435 | CTCTAGCCTGAGAAA[A/G]TCCCAGCAAATAGCA | 74007 |
rs29362533 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85608097 | AGATACACTTATCAT[A/T]CTACATGTAAACAGA | 74007 |
rs29362559 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85506610 | ACAGTGCTAGCATGC[A/G]CTCAGTGGGTTTTCT | 74007 |
rs29362602 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Btbd11 | Mm_Celera | 10:85401084 | CCTGTCCAGCCAGAC[A/G]CTTCTCAACCTCGCA | 74007 |
rs29363224 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85385273 | ACGATAAGTGAGACA[C/T]TCCCCTTAGCAGGAT | 74007 |
rs29363452 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85461046 | TTGAATTGATTTCTT[A/G]TTGTCTCATGCTCAG | 74007 |
rs29363455 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85572449 | CTCTAGTCTAATTTT[C/T]CCATAGGAAAGAAAA | 74007 |
rs29363556 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85511794 | GATTTCTTCTCCAGC[A/G]CAAACCTGTGCAGAT | 74007 |
rs29363560 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85388916 | CCATGCAGTTCTCTC[G/T]CTTGCCCCAGGCCCT | 74007 |
rs29363645 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85619975 | TGGAGCTGGAAGGCA[C/T]TGTGTTAACTGAGAT | 74007 |
rs29363652 | snp | A/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85645633 | TGGAGGATGTCTGTG[A/T]CTGTGACTGTTCTTT | 74007 |
rs29363715 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85427354 | GTCACATTCTTTGAC[A/G]GCATTAGTAAACAGA | 74007 |
rs29363773 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85574186 | AACCAAGCTGGGATA[C/T]AAAGACAGGAAGCAT | 74007 |
rs29363832 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Btbd11 | Mm_Celera | 10:85577668 | CTTGATGGCCAATGC[A/G]AGGGAGAAATTGGCT | 74007 |
rs29364146 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85461065 | TCTCATGCTCAGAGA[C/T]GCTTCCTAGTTTGCC | 74007 |
rs29364238 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85616600 | TATTGCCTGTAGAAC[A/G]GGGAAAGTGGTGGTG | 74007 |
rs29364260 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85573845 | AATATTTGAGACCGT[A/G]TCTTGCTCTGTTGCC | 74007 |
rs29364356 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85629114 | GACATCTTTTTGGTA[C/T]CTCCCTAGCCTGCGT | 74007 |
rs29364442 | snp | C/G | 0.35503 | 0.226867 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85591550 | CAATGCTCCCAACTG[C/G]CAGGGGCTCAACAGG | 74007 |
rs29364461 | snp | C/G | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85447465 | TTCTTGGATTCCTCA[C/G]AGCACTAGAATTGAG | 74007 |
rs29364486 | snp | A/C | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85427585 | ACCATCGAGCTACCA[A/C]GGGCCTTGAATGCCT | 74007 |
rs29365052 | snp | A/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85635171 | CCACTATAACACCAC[A/T]TAAAAGCTTTCTTAG | 74007 |
rs29365071 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85647134 | AGCACCCCTCTGTGG[C/T]CTCTGCATCAGCCCC | 74007 |
rs29365458 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85611929 | GTGGTGTCTCACAGC[C/T]ACATGTAAGTCCAGT | 74007 |
rs29365548 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85472819 | AAGTACTCCCAACCC[C/T]AGCCTTTTTGTGCCC | 74007 |
rs29365659 | snp | A/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85608441 | GACAGTCAACAGAGT[A/T]CTCTCAATGAAAGAG | 74007 |
rs29365735 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85608386 | ATGAGACCCTGTCTC[A/G]AGAAGGACAATGAGG | 74007 |
rs29365823 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85384941 | TGAATGACAAACAAA[A/G]ATGATAGGCATTTAA | 74007 |
rs29365904 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85448680 | TTATTTTTGTCTCAC[C/T]GTTTGAGGGTGTATC | 74007 |
rs29366062 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85626105 | ATGTTTCTTTAAAAC[A/G]GAAGTGTCTCAAATG | 74007 |
rs29366360 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85611964 | GAGGACCTGATGCCC[C/T]CCTCTGGCCTCCAAG | 74007 |
rs29366375 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85393982 | ATAATCTGGTATTGT[A/G]GCGTCTCCCTTCTCT | 74007 |
rs29366475 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85457834 | GTAGCCTTAACTACA[A/G]TGGAGAGGACATCAC | 74007 |
rs29366583 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85391383 | AAACAAACAAGCAAA[C/T]AACAAAACAAACAAA | 74007 |
rs29366711 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Btbd11 | Mm_Celera | 10:85636503 | GCCTAAAAAGAACGG[C/T]GCACCCAGGAGGAGG | 74007 |
rs29366754 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Btbd11 | Mm_Celera | 10:85532296 | GTAGATGCACGCATG[C/T]TTGTGCGCGCCCCCC | 74007 |
rs29366801 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85549238 | TCTCCTTGCAAACAG[A/G]AAGCCAAGAACAAGA | 74007 |
rs29366878 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85384881 | CAGGATGAACGGCAG[A/G]GAATCCACAGCTGCC | 74007 |
rs29366921 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Btbd11 | Mm_Celera | 10:85637221 | CTGCTACTTTTCATA[A/G]ACTTACTGGAGGCCT | 74007 |
rs29367220 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Btbd11 | Mm_Celera | 10:85461333 | AAAAAAAGGAGCTGG[C/G]TCTACACTCCATTGA | 74007 |
rs29367469 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Btbd11 | Mm_Celera | 10:85620548 | ATCCAACTCTTGCTT[C/T]GCCTATTAGCCGAGA | 74007 |
rs29367532 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85612124 | AGCAGGTCACCCATG[A/G]CTGGAGACGTGGCTC | 74007 |
rs29367625 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85647869 | CTGGCACCTGCACTT[C/T]GGGCTCCCTTACGCC | 74007 |
rs29367645 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85577809 | GATCTCTTGGAGTGA[C/T]CAAGGTGGGCCTCCA | 74007 |
rs29367924 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85608209 | GTAGCAGGTAAGTGA[A/G]TACTGCCTGCTTTGC | 74007 |
rs29368657 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85391245 | GCCATGTAATACTAG[C/T]ATGCAGAAGTGGAGG | 74007 |
rs29368888 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85611900 | CAGGGGATACAGTCA[A/G]TTCTCAGCATCACGT | 74007 |
rs29368950 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85610717 | GGGACCCTGCATCTA[C/T]TTTCAGTAATCTTGT | 74007 |
rs29369025 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Btbd11 | GRCm38.p3 | 10:85614974 | ATTAAAGAAAAGATG[A/G]TATAAGATTGTATAT | 74007 |
rs29369054 | snp | A/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85646983 | GCCTCCATGAGATCC[A/T]GCTTAAGGCATTTTC | 74007 |
rs29369164 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Btbd11 | Mm_Celera | 10:85388006 | GGACAGCCGCGTGGC[A/G]CTGCGCATCCACGAG | 74007 |
rs29369236 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85504729 | CACATGGTTTGCACG[C/T]GTGCACATGCACATA | 74007 |
rs29369648 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Btbd11 | Mm_Celera | 10:85420990 | TGCCTGCCCGCAGGA[A/G]CACAGGCTTCTCACT | 74007 |
rs29369984 | snp | C/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85560271 | GAGAGATGCCTCAGA[C/G]GACCTGGGTTTTGCT | 74007 |
rs29370120 | snp | C/T | 0.290657 | 0.246672 | intron-variant, downstream-variant-500B | Btbd11, LOC105245252 | Mm_Celera | 10:85578820 | CCAGGTATAGCAGAG[C/T]CTTGGTGATTATTCC | 74007 |
rs29370295 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85578031 | ACAAGCAAGAGTGTT[A/G]GCCTTGGTTTTTGTT | 74007 |
rs29370596 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85572945 | AAGGCTATGGATAGT[A/G]AACACTTTTATTTTT | 74007 |
rs29370629 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85509607 | GTGACACATGTATTG[C/T]AGACTCTGAGTTCTG | 74007 |
rs29370697 | snp | G/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85618424 | TCAATATGTGGTATG[G/T]GCAAATATTCACATA | 74007 |
rs29370720 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Btbd11 | Mm_Celera | 10:85466655 | CCAGCTGGGCACGGC[C/T]GGGTGCTGCTTGCAG | 74007 |
rs29370849 | snp | G/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85412675 | GTCATGGGTCCTCTG[G/T]GAACCTGCATTGTGT | 74007 |
rs29370898 | snp | A/C | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85427668 | ACCATCGAGCTACCA[A/C]GGGCCTTGAATGCCT | 74007 |
rs29371301 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Btbd11 | Mm_Celera | 10:85446975 | GGCTACTCCACATCA[C/T]ATAAAAGCTGCTCCT | 74007 |
rs29371938 | snp | C/T | 0.277778 | 0.248452 | intron-variant, downstream-variant-500B | Btbd11, LOC105245252 | Mm_Celera | 10:85578469 | CTGGGCATCATGGTG[C/T]GGATGGAAATTTTTC | 74007 |
rs29372034 | snp | A/G | 0 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85614318 | CTGAAGTCGCCTACT[A/G]GCTGAGAATCATTAA | 74007 |
rs29372156 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85647434 | CCAGACAGGAGGGAA[A/G]GCAGGGCAGGCACTC | 74007 |
rs29372301 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85459056 | GTTCATGCTGATGGC[A/G]AGTGCTCTGTTGTCC | 74007 |
rs29372611 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Btbd11 | Mm_Celera | 10:85516495 | CTTTAAAAGTAGAAA[C/G]AGACAATTATTTAGG | 74007 |
rs29372672 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85458081 | AACAAACAAGCAAAC[A/G]AAACATCCAACAATC | 74007 |
rs29372682 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85635143 | TGGTTAAAAATTGCA[A/G]TTCCCTTCCACCCCA | 74007 |
rs29372703 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Btbd11 | Mm_Celera | 10:85575175 | GAAGTAATCCAGGGA[C/T]GAAGTCAGTGCCTCT | 74007 |
rs29372777 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85574761 | CAGGAGTACTCTAAA[A/G]ATTTTGATGCATGAA | 74007 |
rs29373012 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85558109 | GCCTTCTAATGGAGC[A/G]GACTATACTCTTACC | 74007 |
rs29373206 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Btbd11 | Mm_Celera | 10:85456477 | TGAGCCCTTGGACAC[A/G]CCCTTCTCAGTCTGC | 74007 |
rs29373595 | snp | A/C | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85618563 | CACAGAAAGGAAAAT[A/C]CATGACATTAGTTTT | 74007 |
rs29373636 | snp | A/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85608519 | ATGCTTCAAGGACTT[A/T]AAAAAAAAAAAAGTC | 74007 |
rs29373666 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85611972 | GATGCCCTCCTCTGG[C/T]CTCCAAGGTCATCAA | 74007 |
rs29373800 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85386120 | TGCACAAATTTAAGT[C/T]TGAGCAATCTAGAGC | 74007 |
rs29374308 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85391209 | TCTGGGTTCAATTCC[C/T]GGCACTGAATGAACA | 74007 |
rs29374377 | snp | A/C | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85611898 | TTCAGGGGATACAGT[A/C]AGTTCTCAGCATCAC | 74007 |
rs29374572 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85385648 | AACAGGCATGAGCTG[A/G]CAGCTCCTTATGGTT | 74007 |
rs29374861 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Btbd11 | Mm_Celera | 10:85501894 | TACTAACTTTTCATT[A/C]ATATCCTTGCCCCTA | 74007 |
rs29375074 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85503171 | ATCCAGACCATAATA[A/C]CCCCACAGCTCTGTT | 74007 |
rs29375278 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85431070 | GACATGAAATCTCCC[A/G]GGTAAGCTGGCTGGC | 74007 |
rs29375543 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85458373 | GCATTCCTGTCTGCC[A/G]GAAATTCCTCCTGCT | 74007 |
rs29375807 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85639219 | ACATGCCTTTAATTC[C/T]AGCACTTGGGAGGCA | 74007 |
rs29375952 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85426605 | GAGATGGAAGGTGGA[C/T]GAGGACAGAGAAAAG | 74007 |
rs29376013 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85426867 | CTGTGCTTTGGTTAC[C/T]GTCTCCCCTCCCTGA | 74007 |
rs29376281 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85611167 | GGAAAGGGTTTATTC[A/G]GCTTACACTTCCATG | 74007 |
rs29376299 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85409596 | CACATGAAAATGATC[A/G]GCATGGCTATACACA | 74007 |
rs29376502 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85427858 | GAAGTAGGGAAGGTA[A/G]CTGGAAGATGGTGAG | 74007 |
rs29376517 | snp | G/T | 0.484429 | 0.0868505 | intron-variant | Btbd11 | Mm_Celera | 10:85552705 | TGAACATATACATGT[G/T]CTCAAATACAAACTA | 74007 |
rs29377266 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85483197 | CTGCTAGCCAACACA[A/G]CCAAATCTGCCTAGG | 74007 |
rs29377447 | snp | A/G | 0.255 | 0.24995 | intron-variant | Btbd11 | Mm_Celera | 10:85447589 | GATCAGAGCACCGGC[A/G]AACAGGCCTGGGATT | 74007 |
rs29377660 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Btbd11 | Mm_Celera | 10:85600871 | CTGAGGCTGAGGATT[C/T]AGGTACTCAGAGGGA | 74007 |
rs29377704 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Btbd11 | Mm_Celera | 10:85505795 | CTTTGTGTGGCTTAC[A/G]TGCTGCTGGGGAAAG | 74007 |
rs29377840 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85479816 | AAAGAACGTGAACCC[A/G]TTCCTCAGCTACCTG | 74007 |
rs29378132 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Btbd11 | Mm_Celera | 10:85420219 | TCTCTGAGGGACACA[G/T]TGTGTGGAGGATTGG | 74007 |
rs29378146 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85546270 | CTTGGCTACATAATG[A/T]TTGGGGACAGCACCA | 74007 |
rs29378182 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85385260 | TTTTTAGAGTCACAC[A/G]ATAAGTGAGACATTC | 74007 |
rs29378591 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85460303 | TAACAAATTGCAATC[C/T]AGAGAGTATACTGAT | 74007 |
rs29378764 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85608347 | ACTCGGCTACATGTT[A/G]AGTTTGAGACCACTC | 74007 |
rs29378765 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85537456 | GTGGGCGGATGGATG[A/G]ATGGGTAAGTGGGTG | 74007 |
rs29379810 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Btbd11 | Mm_Celera | 10:85469463 | TCACTCTCTGGAGTG[C/T]CTGCCTTCCTGGAGT | 74007 |
rs29379828 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85488093 | GTCCATTATCATCAC[A/G]GCGGGAAAGTATGGC | 74007 |
rs29379923 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85395280 | AGGGTCAGGTAGAGG[C/T]GCAAGGTCACAGGTG | 74007 |
rs29379960 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Btbd11 | Mm_Celera | 10:85524285 | ACAGCCTTGGAGGTA[A/G]AAGATTTAGGAGGCA | 74007 |
rs29380168 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Btbd11 | Mm_Celera | 10:85421666 | AATGAAGCGCTTCTC[C/T]AGCTTTCTATTACAG | 74007 |
rs29380544 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85449064 | GGCGTGGTGGAGCAG[C/T]GCTTTCAGGGGTTTG | 74007 |
rs29380581 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85409653 | GAGATGGGAGTCCCA[A/G]GGCTTGCTGGGCAGT | 74007 |
rs29380597 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85636084 | AAATGTCACTTTGAA[A/G]TATGACATACACTTA | 74007 |
rs29380735 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Btbd11 | Mm_Celera | 10:85575045 | CCCTGAAAGGGGTAC[C/T]AAGTGCCTAAGAGAG | 74007 |
rs29380767 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85634105 | TACCAATGAGTAATT[A/T]AAAGCTGTGGGTCAG | 74007 |
rs29381026 | snp | G/T | 0.33241 | 0.236027 | intron-variant | Btbd11 | Mm_Celera | 10:85649447 | ACTCCTTAGCATCAC[G/T]CGTGTACAAAAGCCA | 74007 |
rs29381362 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85512921 | TGTGCCTCTTGAATG[C/T]CTGGATGTATTCCTG | 74007 |
rs29381588 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Btbd11 | GRCm38.p3 | 10:85597363 | GCCTCTTAAACCACG[C/T]CCCTCCTCAGGTGAA | 74007 |
rs29381922 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85619821 | AGAGGGAATTGGAGT[C/G]AACCTAATTGTCCAT | 74007 |
rs29382218 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85612128 | GGTCACCCATGACTG[A/G]AGACGTGGCTCCATG | 74007 |
rs29382389 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85586725 | AGCTGTGCCAGCCTG[C/T]GCCCGTTAGAGGCTT | 74007 |
rs29382407 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Btbd11 | Mm_Celera | 10:85513210 | TGTGTATATGCTTGC[A/G]CTAACAGTGTACTTG | 74007 |
rs29382636 | snp | C/T | 0.444444 | 0.157135 | missense | Btbd11 | Mm_Celera | 10:85388329 | CAGCCACCGCCGCCG[C/T]CGCCGCCAACCATCA | 74007 |
rs29382789 | snp | C/T | 0.255 | 0.24995 | intron-variant | Btbd11 | Mm_Celera | 10:85447644 | TGCTCTGTGTTCTGC[C/T]GTCAAAAATTATGAA | 74007 |
rs29383459 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Btbd11 | Mm_Celera | 10:85461371 | ATGTGCATCTTTTCA[C/T]AGGCTCTCTGGTTTT | 74007 |
rs30141855 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85407810 | TTTAAATGCATTGGA[G/T]AGCCTAGTGCCAGAT | 74007 |
rs30141857 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85408157 | CAGGTGGGCACACTC[A/C]TGCAGCTGGGACTGG | 74007 |
rs30141860 | snp | A/C | 0.18 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85408625 | AGCAGCAGGAATTCG[A/C]GTGGGGCTGCTGAGG | 74007 |
rs30141863 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85408891 | TAGTACAGAGAAGCC[A/G]TTTGGCAGTCAGATG | 74007 |
rs30141865 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85420121 | GTATCAAGGTGATCA[C/T]TCAAAATTCTGCATC | 74007 |
rs30141868 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85420285 | GAATACATGGAACTA[C/T]GGGAGTCGTGGGAGT | 74007 |
rs30141870 | snp | G/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85420359 | GAGGTAGGAGGATTT[G/T]AACTTTTGGGTATCC | 74007 |
rs30141871 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Btbd11 | Mm_Celera | 10:85420394 | ATGCTTCGTCCTTTT[C/G]TTCCATTCCCTTGCA | 74007 |
rs30141873 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85420439 | TACCTGTATTGATTA[C/T]ATTTAATAACTACCT | 74007 |
rs30141906 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85430613 | AGCACAAGAAAGCTA[A/G]GGATATTGGAGAGTT | 74007 |
rs30141908 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85430730 | GTTCTGGCACTGCCA[A/G]CGTAGTATTTTATGT | 74007 |
rs30141910 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85430849 | ATGCTTCTCCATTAC[A/G]TAGGGTTTGCTTGGG | 74007 |
rs30141912 | snp | A/C | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85430901 | TACACACGTAGCAGG[A/C]GACATTAAAAACACG | 74007 |
rs30141926 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85400899 | TAGCTTCAAATAGCT[A/T]GATGCTTCAAAGAAG | 74007 |
rs30141929 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85401130 | TGTCATTTGTCAGGG[C/T]CAGCAGCAGCATCTG | 74007 |
rs30141931 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85401182 | AAAACTGGCTTGCCT[C/T]TGGAACTCGGAGAGG | 74007 |
rs30142365 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | GRCm38.p3 | 10:85437494 | TTGCTGTAATGGAGC[C/T]GGAGAACAGATTTCC | 74007 |
rs30142367 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Btbd11 | GRCm38.p3 | 10:85437930 | tctctctctctctct[A/C]AAAAGCCACTTTGTT | 74007 |
rs30142369 | snp | A/C | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85437980 | GACCTCTGGGAGCTA[A/C]GGTGGATATAATCTG | 74007 |
rs30142371 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85438010 | GTCCTTTCTCGCTAT[A/G]GTGCGTACCCCTGGA | 74007 |
rs30142373 | snp | G/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85438016 | TCTCGCTATAGTGCG[G/T]ACCCCTGGAGGCCAT | 74007 |
rs30142794 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85430916 | AGACATTAAAAACAC[A/G]ACATCTAGGCTGGAC | 74007 |
rs30142796 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85433750 | AAATTTAAACATGGG[C/T]TTAACATCAAACAGA | 74007 |
rs30142798 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85433755 | TAAACATGGGTTTAA[A/C]ATCAAACAGACCTGA | 74007 |
rs30142800 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85433763 | GGTTTAACATCAAAC[A/G]GACCTGAGTTAGACT | 74007 |
rs30142802 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Btbd11 | Mm_Celera | 10:85433803 | AGCAAACCTACTGAA[C/T]GTGTGTTATTTTCTA | 74007 |
rs30142965 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85409082 | TCTGTCAGGAATCTC[A/G]GATACCAGGCACAAA | 74007 |
rs30142967 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85409453 | AGTTGGACTCTTTAT[C/T]GTTGAAGAGATTTCA | 74007 |
rs30142969 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85409454 | GTTGGACTCTTTATC[G/T]TTGAAGAGATTTCAA | 74007 |
rs30142971 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85409802 | AAAACATAGTAGCAA[A/G]CTATTTTACTTTGAT | 74007 |
rs30142973 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85409888 | TCGGGTACGGTAGGG[C/T]CAAGTTGCTGGCTGG | 74007 |
rs30143015 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Btbd11 | Mm_Celera | 10:85401432 | GATGTAGTTTCTTTG[A/C]GTGGCAGTGTGGCCC | 74007 |
rs30143017 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85401749 | AAGAACCTTTTGCTC[A/G]CCATGGCCTAATTGA | 74007 |
rs30143019 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85401791 | CTGCCTCTGTGTTTC[C/T]GAATTCTCATCCCTG | 74007 |
rs30143021 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85401944 | CCAATGTCAGTACGG[C/T]AGCTTGGATCTTGAG | 74007 |
rs30143023 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85402112 | AAAGGAAGATGCTGA[A/G]CTTGAGAGACTGAAA | 74007 |
rs30143064 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85420702 | TATGGCTTCTCCAGT[C/T]GGTCATCCAGGTTGT | 74007 |
rs30143066 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85420750 | CCACCAAAGGCAATA[C/T]AGGTCCTGGTGCACC | 74007 |
rs30143068 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85420753 | CCAAAGGCAATATAG[A/G]TCCTGGTGCACCTTG | 74007 |
rs30143070 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85420875 | TTTGTGTGTGAAGGC[A/G]CAGAAAGACAGGGAC | 74007 |
rs30143072 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85420905 | CTTGGAGAAGAGGAG[A/G]CAGGGTTCCGTGGAG | 74007 |
rs30143175 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Btbd11 | Mm_Celera | 10:85438125 | CAAAGGAATAGAGGC[A/G]GCCTGCACTTTTCCT | 74007 |
rs30143177 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Btbd11 | Mm_Celera | 10:85438156 | CTTTCCTTTTCTCTA[C/T]AGCTCTCAGATACAA | 74007 |
rs30143179 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85438173 | GCTCTCAGATACAAC[A/C]GATAATTGAGTCGTA | 74007 |
rs30143181 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Btbd11 | Mm_Celera | 10:85438189 | GATAATTGAGTCGTA[A/C]GTTCATGACCGCTTC | 74007 |
rs30143183 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85438197 | AGTCGTAAGTTCATG[A/G]CCGCTTCACCGCCAT | 74007 |
rs30143521 | snp | A/C | 0.21875 | 0.248039 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85384799 | TTCTGATATTAGAGA[A/C]CAGGAAAGGGAACGT | 74007 |
rs30143523 | snp | C/T | 0.408163 | 0.193609 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85384812 | GAACAGGAAAGGGAA[C/T]GTGTTGCTATGGACG | 74007 |
rs30143634 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Btbd11 | Mm_Celera | 10:85434144 | CAAACCATAGCACCC[A/G]TTACCTGAACTTTAT | 74007 |
rs30143635 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85434280 | GGTCCGAAATGAAAT[A/G]TTCCTAGGCTATATT | 74007 |
rs30143637 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85434284 | CGAAATGAAATGTTC[C/G]TAGGCTATATTTGTT | 74007 |
rs30143639 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85434307 | TATTTGTTCCTGCTG[A/G]TCTGGAGACTTGTGG | 74007 |
rs30143641 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Btbd11 | Mm_Celera | 10:85434318 | GCTGGTCTGGAGACT[C/T]GTGGCGAGCAAGTTC | 74007 |
rs30143643 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85434483 | CTCTCCACCAAGCTC[A/G]TAAGTATATCAGGCT | 74007 |
rs30143705 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85409979 | TGGACTCTTCTCTGC[A/G]TTATATCATATTTCC | 74007 |
rs30143706 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85409988 | CTCTGCGTTATATCA[C/T]ATTTCCCAGGACTCA | 74007 |
rs30143708 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85410103 | GATTGGTTAAAAGCC[A/G]TGTCCAAAAGTAGTG | 74007 |
rs30143710 | snp | G/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85410202 | ACAAGAGACTTTGCC[G/T]CTTTGGAAAATGGTT | 74007 |
rs30143712 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85410581 | CAGTTACAATTTAGT[C/T]ACAAGGCAGAGTATT | 74007 |
rs30143725 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85402251 | TTCTCTGTCTTTACC[C/T]GTGATCTTGTCCAGT | 74007 |
rs30143727 | snp | C/T | 0.18 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85402623 | AAAGATCCACCTGCA[C/T]GCACCACCACACCTG | 74007 |
rs30143730 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Btbd11 | Mm_Celera | 10:85403214 | TGGATTCAGTGAGGT[A/C]TTTTTTTTCTCTCCC | 74007 |
rs30143732 | snp | A/C | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85403273 | TTGGGGTGAGCATGC[A/C]TTCCAGGCTGGAACT | 74007 |
rs30143874 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85420942 | GGCATGCAGAGAGGT[A/G]AACACTTCAGAACTC | 74007 |
rs30143877 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Btbd11 | Mm_Celera | 10:85421098 | GTGGGCTGACTGTGC[A/G]CTGGTCCATGCCTCC | 74007 |
rs30143879 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85421159 | CCAGCAGAAGCCTTT[C/T]TGGAAGCCTTGGAGG | 74007 |
rs30143882 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85421811 | CTTTAAAGTTACATC[A/G]CTGGCAGACCACAGG | 74007 |
rs30144025 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85438228 | TAGTACCACCTTGCT[A/C]GTTTTAGACTTCAGT | 74007 |
rs30144027 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Btbd11 | Mm_Celera | 10:85438354 | AGGCATGGCTGTGTG[C/T]GCATGTGAGCACACA | 74007 |
rs30144029 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85438443 | TTTTACCTATGTTCT[A/C]TTGTTTTCAAGATCC | 74007 |
rs30144031 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85438515 | TGGTTGAGCCAGTGA[C/T]GGTCAGTGAAGTTAC | 74007 |
rs30144033 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85438599 | CTACCTGGCCATACT[A/G]CATGTCCTTTGGTTT | 74007 |
rs30144535 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85386031 | GCCAAGCAATGATGC[C/T]GTTAGACACAGAAAT | 74007 |
rs30144537 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB | Btbd11 | Mm_Celera | 10:85386103 | AAAAGAATATTCTCC[C/T]GTGCACAAATTTAAG | 74007 |
rs30144540 | snp | G/T | 0.489796 | 0.070696 | utr-variant-5-prime | Btbd11 | Mm_Celera | 10:85386976 | GACACTGTGGCCGGC[G/T]CTCGGAGGCTTCTGC | 74007 |
rs30144542 | snp | G/T | 0.489796 | 0.070696 | synonymous-codon | Btbd11 | Mm_Celera | 10:85387352 | GAGAGGTAAGAAGCC[G/T]GTGGTGCGAACGCTG | 74007 |
rs30144685 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85434501 | AGTATATCAGGCTTT[G/T]ATCCAGACCCAACTC | 74007 |
rs30144687 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85434655 | AATCACCCATGACCA[A/G]GTTCTACAGGCTGGG | 74007 |
rs30144689 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85434689 | AGCTATTGGAAATAC[C/G]CACCAACATGGACAG | 74007 |
rs30144691 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85434719 | GAGATAGCTGCCAAA[C/T]TCCTTGCCTGGTCCT | 74007 |
rs30144693 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85434877 | CAATAAGCAGCTACT[C/G]AAAGCAATGGAAGCA | 74007 |
rs30144794 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85403348 | ATCAACATACTCAGA[C/T]TGTAATTTTGGATCC | 74007 |
rs30144796 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85403361 | GATTGTAATTTTGGA[C/T]CCTTATTTATCTTAT | 74007 |
rs30144798 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85403401 | TTCTCTACATGTGCA[C/T]GGCTTGCAACATCCT | 74007 |
rs30144800 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85403412 | TGCATGGCTTGCAAC[A/G]TCCTGCCACTCACTT | 74007 |
rs30144802 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85403682 | GGCTGCTCAGGACAC[A/G]CAGTTGGCTCTGACT | 74007 |
rs30144834 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Btbd11 | Mm_Celera | 10:85422169 | CAAGTGCTCAGAATA[A/G]GTAAGTGGTAACAAG | 74007 |
rs30144836 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85422985 | TCCGTTCCCAAACAT[A/C]GTGGCACCCTAGAGG | 74007 |
rs30144838 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Btbd11 | Mm_Celera | 10:85423060 | AGAACAATGGATGAG[A/T]AAGATTTGTCAGGAA | 74007 |
rs30144839 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85423174 | TTTGAAATCTGACCT[C/T]TGTTGAAGTTGAAGA | 74007 |
rs30144840 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Btbd11 | Mm_Celera | 10:85423217 | GTCAGCACTACCTCA[A/G]AATTCAAAACACAAT | 74007 |
rs30144841 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Btbd11 | Mm_Celera | 10:85423242 | CACAATTCAGCTCCC[A/G]TGAACTTGGCAACCA | 74007 |
rs30144843 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Btbd11 | Mm_Celera | 10:85423291 | TCCCAATGGAAAGAG[A/G]TGGCAACCCATGGGT | 74007 |
rs30144915 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85438688 | AGAGAGGAGGAAGGG[A/G]CAAGATACTTACTCT | 74007 |
rs30144917 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Btbd11 | Mm_Celera | 10:85438747 | AATGGCACAATGAGT[C/T]CTGAATCCTTCTGTC | 74007 |
rs30144919 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Btbd11 | Mm_Celera | 10:85438760 | GTTCTGAATCCTTCT[A/G]TCCAAAAGGGGTCCA | 74007 |
rs30144921 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85438768 | TCCTTCTGTCCAAAA[A/G]GGGTCCAAAATAAAT | 74007 |
rs30144923 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85438877 | AATTGGCAAATGGAT[C/T]TGATGACTGTCATAC | 74007 |
rs30145046 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Btbd11 | Mm_Celera | 10:85410697 | GCAACAGGCCTGACT[A/C]TTGAAAAGTGAATAG | 74007 |
rs30145048 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85410830 | AGAAAGCCTTCCTCC[A/G]TACTTCGTTGCTTAT | 74007 |
rs30145050 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85410882 | TGTTTTCCATATGCA[C/T]ATTCAGTGTGTATGC | 74007 |
rs30145052 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85410935 | GTGCACAAAATATAT[A/G]CAAACCCATAGATAT | 74007 |
rs30145565 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85434892 | CAAAGCAATGGAAGC[A/G]TCACAGAGTGAAAGG | 74007 |
rs30145566 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Btbd11 | Mm_Celera | 10:85434997 | AGGTGCCCATGGGAG[A/C]CTGAACAGGAATATC | 74007 |
rs30145567 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85435030 | ATTGTGAGAACACAC[C/T]GCACCACGTTGTCGT | 74007 |
rs30145569 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85435037 | GAACACACTGCACCA[C/T]GTTGTCGTAACGTAG | 74007 |
rs30145570 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85435054 | TTGTCGTAACGTAGC[G/T]GCTGTGAGCCTCTTT | 74007 |
rs30145572 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85435104 | GGAAGCTTCTGAGAA[C/T]GGGCCGCATCCTTTT | 74007 |
rs30145573 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85435286 | AAGGGAGGAAATAAG[A/G]AACCTCAAGAAGGCA | 74007 |
rs30145614 | snp | C/T | 0.408163 | 0.193609 | synonymous-codon | Btbd11 | Mm_Celera | 10:85387374 | CGAACGCTGGAAGAT[C/T]TGACGCTGGACTCGG | 74007 |
rs30145617 | snp | A/C | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85388640 | TCCGCGTGGTTGACA[A/C]TGGTAGTAATGTTCC | 74007 |
rs30145619 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Btbd11 | Mm_Celera | 10:85391690 | CTGACGATCTAAACC[A/G]GCAGCACTAATTTTG | 74007 |
rs30145621 | snp | G/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85392861 | CTATCTTGCCAGTAC[G/T]TGAATCCTCTTTTGA | 74007 |
rs30145623 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85393409 | CTTGTATTAATTTTT[A/G]GGTGCTTTAAAAGCC | 74007 |
rs30145694 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85403774 | CCCAATGGAGTCTGC[C/T]GTAGCTAGCCTCACC | 74007 |
rs30145696 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85403844 | GAACCCTGAAGGCAG[C/T]GGACTTTGAGCCTTA | 74007 |
rs30145698 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85403888 | ATGGTCAGGAAGCCC[G/T]TGCTTGAAACATGCT | 74007 |
rs30145700 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85404020 | GAAGGAATGTGTCAC[A/C]ACCTCAAGCTCCCTG | 74007 |
rs30145702 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85404092 | ATTCTGATCAGACTT[C/G]TCCTGAAGGAACACA | 74007 |
rs30145855 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Btbd11 | GRCm38.p3 | 10:85423813 | GAGCCCTGAGGTATG[G/T]GAATGAGGGAGCCCT | 74007 |
rs30145857 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Btbd11 | Mm_Celera | 10:85423963 | GATGCATTGATTTGG[A/G]CCTTAATGAAGCGGC | 74007 |
rs30145859 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85423975 | TGGACCTTAATGAAG[C/T]GGCTGGCTGGAGTGA | 74007 |
rs30145861 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Btbd11 | Mm_Celera | 10:85424034 | GTTTATGGGATGTAG[C/T]GGATCTCAGAAAGGA | 74007 |
rs30145863 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Btbd11 | Mm_Celera | 10:85424153 | CCACAGTCCATTTTA[A/G]GATTGTGAAGGCCCC | 74007 |
rs30145875 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Btbd11 | Mm_Celera | 10:85438932 | TCTGTTCATTCATTA[C/T]CTCCAGTTCCTCACC | 74007 |
rs30145877 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85438948 | CTCCAGTTCCTCACC[A/G]CTACAGACTCAGTGC | 74007 |
rs30145879 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85439037 | CCACACCCAGAATTG[A/G]GCTTGTTGTCTGTTA | 74007 |
rs30145881 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Btbd11 | Mm_Celera | 10:85439100 | TTCTGGTCTTCCCAG[G/T]CCATTGACTAGAATA | 74007 |
rs30145883 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85439177 | ATGGGTTTAAGCATC[A/G]TTTTAGATAGTCACT | 74007 |
rs30146134 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85411050 | ATGCCACATGCCTAC[C/T]AGACAATATTTTAAG | 74007 |
rs30146137 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85411158 | GGGGTGTTATTTCAC[A/G]TGGAGCTACATGATA | 74007 |
rs30146140 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85411243 | TTATTATGAAAGAGT[A/G]TACTTCTGAGAGAGG | 74007 |
rs30146142 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85411387 | TTTGGGATCATTTGT[A/G]TAATGCAAAAAGGAT | 74007 |
rs30146544 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85404136 | TCATGGGTCTAGTGG[A/G]CAATCCATTCTCTGT | 74007 |
rs30146545 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85404299 | TGCTGTGGTTCGCAG[G/T]CATGCACAGGGTTTT | 74007 |
rs30146547 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85404386 | CATACTGGGAGCCAT[C/T]AAGAACAGCTGTGTG | 74007 |
rs30146549 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85405331 | TCAGGTTGAGTTTCG[C/T]TGGCTAACATTTGTA | 74007 |
rs30146551 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85405350 | CTAACATTTGTATAC[A/T]ACTGTGGAGGAGACA | 74007 |
rs30146615 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85424256 | TATGAGTAGCCACTG[A/G]TGTGGTCCAAGATGG | 74007 |
rs30146617 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85424440 | GGTATAGGCTTACAC[A/G]ATGGAGTCATTGGCG | 74007 |
rs30146618 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Btbd11 | Mm_Celera | 10:85424572 | CTGTGGATGGCCACA[A/G]GTCTTCCTGTTTCTG | 74007 |
rs30146620 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85424653 | AGAGAACCCACTGTC[C/T]TCCAGAAGTCATGAT | 74007 |
rs30146622 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85424753 | CTTATCACTGGCTTC[A/T]CATGACCCGATAAAT | 74007 |
rs30146685 | snp | C/G | 0.197531 | 0.244432 | intron-variant | Btbd11 | Mm_Celera | 10:85393433 | AAAAGCCTGGGCAGC[C/G]TGGAAGAGACCCCAA | 74007 |
rs30146687 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85393578 | CCCTCAGAATTAGTC[A/G]TTTTCCGCTCAACCT | 74007 |
rs30146690 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85398284 | GTGTAGTGGCTATTA[G/T]GTTTAAATGGTTATG | 74007 |
rs30146692 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85398427 | AAGCATGGACTGACC[G/T]CAGGGTATAGGGTAA | 74007 |
rs30146725 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85435344 | TAATGAGTCTCCTGG[A/G]AATCAAGAAGTGAAC | 74007 |
rs30146727 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Btbd11 | Mm_Celera | 10:85435398 | TTTAAAAAAGGAAAA[A/G]GGAAAAACCCTAACA | 74007 |
rs30146729 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85435470 | AATGCTGCGGCGAAG[A/G]AGAAATGTGCATGAT | 74007 |
rs30146731 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85435642 | AGCTCCTAATTGGGA[A/G]GTTTAGCAAATACAT | 74007 |
rs30146733 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85435680 | TGAAAATGAAAGTGA[A/G]GTGGAAAATACACAA | 74007 |
rs30146815 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85439237 | TCTTATCACTCAGCC[A/G]TTTTCCTGTCCCATG | 74007 |
rs30146817 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85439265 | ATGTCCTACCTTTGC[C/T]GTCCATTGATTGTAA | 74007 |
rs30146819 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85439770 | ATGGTATATGGGAAG[A/G]ATCCAAGTTCATCCA | 74007 |
rs30146822 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85440882 | AAGAAAAAAATCTCT[A/G]GCTCTAGGAGTTAAA | 74007 |
rs30147264 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85411829 | CTTGGGTAGCACGTT[C/T]CCCACGAGCTGTGGG | 74007 |
rs30147266 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85411879 | GGGATGCTGATCACC[C/T]TAATAACTTCTTACT | 74007 |
rs30147268 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85411956 | CTCTGTCCATTCATC[A/G]AGGATCTGGATTGGC | 74007 |
rs30147270 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85412010 | CCCACATCACAGCCA[C/G]TTTAGTCTGGAGCTG | 74007 |
rs30147272 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85412101 | AACTAGCTTATGCCA[A/G]TCACTGGCCCCAGAA | 74007 |
rs30147615 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85435829 | ACATAATGGCAGGCA[C/T]GCAAGGAGGAGGGCC | 74007 |
rs30147617 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85435938 | CACTTTCCATATCCT[C/T]GCCACATTTTTTCTT | 74007 |
rs30147619 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85435954 | GCCACATTTTTTCTT[C/T]CTGCTGCACAATTTA | 74007 |
rs30147621 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85436219 | CTCTATGCGTTGTGT[C/T]ATCTTCATCTCAATA | 74007 |
rs30147623 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85436240 | CATCTCAATATGGTG[A/G]CTCTTACTCCAAGAC | 74007 |
rs30147644 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Btbd11 | Mm_Celera | 10:85398754 | GGAGAGTCCGTGATT[A/C]AATCTGTGTCGTAAG | 74007 |
rs30147646 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85398811 | GAACAAAAGACTGAA[C/T]GCTGGAAGGCTAGTT | 74007 |
rs30147648 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85398953 | CGTTTTCCTCATCCC[A/T]AGGAAGTTTATGGTT | 74007 |
rs30147650 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85399106 | TGGGAAGGTGACCAC[C/T]GTCTATTTCCTCCTG | 74007 |
rs30147653 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85399398 | CAGGGTGGCTGCCAA[A/G]GAAAGGGACTGAAAT | 74007 |
rs30147724 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Btbd11 | Mm_Celera | 10:85425065 | GCTACCAGATTGACC[C/T]GTATGTCACTTAACG | 74007 |
rs30147726 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85425074 | TTGACCTGTATGTCA[C/T]TTAACGACTTTTGTC | 74007 |
rs30147728 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85426798 | CACGCAGTGGAGTCA[A/G]ACCCCAGAGTCAAGG | 74007 |
rs30147731 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85426957 | GCCTGAACATCCAGG[C/T]TCTAAGAGAGTGAAA | 74007 |
rs30147733 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Btbd11 | Mm_Celera | 10:85426995 | GGGTACTGGAATAGC[C/T]GAGCCTGATCCTGTT | 74007 |
rs30147734 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85405406 | CCAACAAACAGACCT[C/T]ATTGCATTCACTGTG | 74007 |
rs30147736 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85405473 | CATTAATTACTGCAT[A/G]ATCATATTCTTGCTG | 74007 |
rs30147738 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85405783 | GTCAAGGAGCCTAGT[G/T]GAGGCTGGCCTGAAA | 74007 |
rs30147740 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85405837 | CCGCAACTGAGGCAT[C/T]GCCAACATTCTCACA | 74007 |
rs30147743 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85406108 | TGGTCAGGCCAACTT[C/T]CCATTGTAGTGAGCA | 74007 |
rs30148124 | snp | A/C | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85412138 | AAATCTAGGAAATAA[A/C]TGGCCCTGTGTATTC | 74007 |
rs30148126 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85412229 | GTTAGTATGGTTTTT[C/T]AGTTCAAGAGTGGGA | 74007 |
rs30148128 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85412313 | TCATGGCAACAGCAG[A/G]CAGTGAGGGAGCAGG | 74007 |
rs30148130 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Btbd11 | Mm_Celera | 10:85412659 | CTCACCTTTTCCTTG[A/T]GTCATGGGTCCTCTG | 74007 |
rs30148133 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85412758 | TCAAGGCCCCCTTGA[C/T]CAGTAGCTGACGTGT | 74007 |
rs30148545 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85436260 | TACTCCAAGACCATT[A/G]TTACAACCAGAGATC | 74007 |
rs30148547 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Btbd11 | Mm_Celera | 10:85436333 | AGCAATTTTGGAGTC[C/T]TTATGTGATTTTCCT | 74007 |
rs30148549 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Btbd11 | Mm_Celera | 10:85436352 | TGTGATTTTCCTCAC[A/G]TGTCACATGACTGAC | 74007 |
rs30148551 | snp | A/G | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85436395 | GTAGAGAATCTAAGA[A/G]CCAAAGTATTCCATT | 74007 |
rs30148553 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85436870 | ATGGTTCCTTCCATG[A/G]TGACTAGCTCAAATT | 74007 |
rs30148635 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Btbd11 | Mm_Celera | 10:85427076 | TGTTCTCAGTGTTGG[C/T]TGCCAGGCACCTGGC | 74007 |
rs30148637 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85427777 | TGCCTTCTGGAAAGA[C/T]TGCAATGACTTGATA | 74007 |
rs30148642 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85429499 | CACAACGTAAAATTT[C/G]CAAAGACTCCATTTT | 74007 |
rs30148645 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85399450 | TCAGAGGCAAAGGTC[A/C/G]TGTGGATTAACTGCT | 74007 |
rs30148647 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85399470 | GATTAACTGCTTTTC[A/T]TTGTGTGGCTTGTCT | 74007 |
rs30148649 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85399577 | CAACTTCTCTTTTCC[C/T]TGATGTCTCTAGGAA | 74007 |
rs30148651 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85399804 | ATGGGACTTTCAAGG[C/T]CTATTCCTTGTCAGC | 74007 |
rs30148653 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85399997 | CCTGTCTTGCTCTGC[C/T]CCTGCTTCAGTCTTT | 74007 |
rs30148745 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Btbd11 | Mm_Celera | 10:85406197 | CTTCTGGAAGGTTCA[A/C]CAGAGAACTTCTAGG | 74007 |
rs30148747 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85406639 | AGCTCCTGTAAACCT[G/T]CACATCCCCACGTGT | 74007 |
rs30148749 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85406656 | ACATCCCCACGTGTG[C/T]TTGCAGAACTGTCCA | 74007 |
rs30148751 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85406795 | TAGTGGGTGCCTGGG[C/T]ATTTCTGAAGATGAG | 74007 |
rs30148753 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85406871 | CGATGACATGCTGTG[C/G]ACTTGCCCGGTCCCT | 74007 |
rs30149035 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Btbd11 | Mm_Celera | 10:85412995 | TGTGAGTGATATTAC[A/G]ACTCAGGAAGCGGAC | 74007 |
rs30149037 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85413007 | TACAACTCAGGAAGC[A/G]GACTGGGGTTCCCAA | 74007 |
rs30149039 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85413024 | ACTGGGGTTCCCAAC[A/G]GGAATGGTGACTCAT | 74007 |
rs30149041 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85413296 | TTTATTGTGTTCTGA[A/G]TGTTACGTTTTACTG | 74007 |
rs30149043 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Btbd11 | Mm_Celera | 10:85419771 | CACAGAGAGCTGGGA[C/T]GCACCTGTCTCATCT | 74007 |
rs30149385 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85436909 | TGTGGGTTGATGGTG[C/T]ATGCTTTTGCAGTTT | 74007 |
rs30149387 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85436921 | GTGTATGCTTTTGCA[G/T]TTTGTCTTACTTATC | 74007 |
rs30149389 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85437035 | GGGTTTGATCATTGA[A/G]ATTCCTTATTTACAT | 74007 |
rs30149392 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85437173 | GCTTCTACTGAATGC[C/T]CATACAGTTGCTAGA | 74007 |
rs30149435 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85406940 | CTACCAGACTTATTC[C/T]ATCTGCCACGATGTC | 74007 |
rs30149437 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85406951 | ATTCCATCTGCCACG[A/C]TGTCTGAGAACCACT | 74007 |
rs30149439 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Btbd11 | Mm_Celera | 10:85407011 | ACCAAGAACCTCTGG[A/G]CCACAGGAAGCCTTC | 74007 |
rs30149441 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Btbd11 | Mm_Celera | 10:85407044 | CCTTCTCCTAATCTC[A/G]GTCCATCATGACTGA | 74007 |
rs30149443 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85407092 | AAGGACTGCAGGGTC[A/G]AGCGAAAACTCTTCA | 74007 |
rs30149465 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85400094 | GGAGATGCTCTCATT[A/G]ACAGAAACGGATGGT | 74007 |
rs30149467 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85400102 | TCTCATTGACAGAAA[C/T]GGATGGTGTTCAGGA | 74007 |
rs30149469 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85400307 | ACACCTCATGAGAAG[C/T]CTGAGTGGTCCGTGG | 74007 |
rs30149471 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85400358 | AAAGAGGGCAGATAG[C/T]GGTAGGTGACACTGA | 74007 |
rs30149473 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85400385 | CTGAGGTATCAATTC[A/C]ACAGCCTGGGAGAGT | 74007 |
rs30149654 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Btbd11 | Mm_Celera | 10:85429927 | CCTTTTTAAGGCAAG[C/T]GACTTTGGTGTTTCT | 74007 |
rs30149656 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Btbd11 | Mm_Celera | 10:85429953 | TTTCTTTGTTGCATG[C/T]TGTTTGATTCTCTTA | 74007 |
rs30149658 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | Mm_Celera | 10:85430034 | TTGTCATTAGTATTT[C/T]GGATGGGTTAAAAAA | 74007 |
rs30149835 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Btbd11 | Mm_Celera | 10:85419772 | ACAGAGAGCTGGGAC[A/G]CACCTGTCTCATCTA | 74007 |
rs30149837 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85419891 | GTGTGACGGATGTCA[C/T]GAAGCATTTGCTTTT | 74007 |
rs30149839 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85420016 | TCACTTTCTGCAGCC[C/T]GTTTCAATGTAGAAT | 74007 |
rs30149841 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85420087 | TTGCTTTCCATTTGG[C/T]GATCCCTGTATCTCT | 74007 |
rs30150335 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85407772 | AGGTGAATGTGTCAC[A/G]CTTGACCAACAGTGA | 74007 |
rs30150425 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85400472 | GCCCATCAGACCCAC[A/G]TTATCTGCCATGAAC | 74007 |
rs30150464 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Btbd11 | Mm_Celera | 10:85437304 | TTATTACTTTAATCA[A/T]TAGATAAACTGAGGA | 74007 |
rs30150466 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Btbd11 | Mm_Celera | 10:85437456 | AACTTTACTTGTCAC[A/G]CACACTCTTGTTTTC | 74007 |
rs30574683 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Btbd11 | GRCm38.p3 | 10:85541895 | ACCTGGGTCAGGGAT[A/G]TACTTCCCCATGAGG | 74007 |
rs30674584 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | GRCm38.p3 | 10:85541838 | CCTTCCCCCACCCAC[C/T]CTCAGGGACGATGCT | 74007 |
rs30879832 | snp | G/T | 0.5 | 0 | intron-variant | Btbd11 | GRCm38.p3 | 10:85541684 | TTCAGTCTAAGCTCC[G/T]CCCCACAGTTATCTG | 74007 |
rs31020874 | snp | C/T | 0.5 | 0 | intron-variant | Btbd11 | GRCm38.p3 | 10:85541704 | CACAGTCAGACTTGT[C/T]AGCATTCAGTCTAAG | 74007 |
rs31092425 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | GRCm38.p3 | 10:85606250 | AATAAATAAATATAA[A/C/T]AATAATAATAATAAT | 74007 |
rs33849664 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Btbd11 | Mm_Celera | 10:85639911 | GGATGAAGGTCACCC[A/G]GAGCAGTCTCCTTCC | 74007 |
rs33850323 | snp | A/G | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85427190 | TATGCATGACCCACT[A/G]TCAAGAGATTTAAAA | 74007 |
rs33850552 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85519995 | GTAAGACTTTGCCCC[A/C]AAAATCATCCAACCA | 74007 |
rs33850682 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | Mm_Celera | 10:85574752 | CTTATGGGGCAGGAG[C/T]ACTCTAAAGATTTTG | 74007 |
rs33880961 | snp | G/T | 0.375 | 0.216506 | intron-variant | Btbd11 | GRCm38.p3 | 10:85648917 | GCGGGGGTTGGGGGG[G/T]TGTCATGAGCTGAAG | 74007 |
rs33881211 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85486299 | AAACCCAGGGCTTCA[C/T]ATAAATAAGCCAAGC | 74007 |
rs33881247 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85648854 | CCTGGGGACATGAGT[C/T]GGCTCTGGAGTCACC | 74007 |
rs45635470 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85624203 | GCAGTAGGTTCTGCA[C/T]TCGGGAGCTAGAGTG | 74007 |
rs45638497 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85397678 | CTAGTATTCTTACAC[A/G]TGGTCTTAACTCCAT | 74007 |
rs45641824 | snp | C/T | | | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85587617 | AGCTCTTCATCTCAA[C/T]AGTTTTGGTTTTCTT | 74007 |
rs45643572 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85397569 | TGTTTTTCATGTATA[A/G]TCTAGTTAATGACAG | 74007 |
rs45644463 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85613698 | CAAGCGGGTGCAATT[C/T]CTGGACTGGGATTTC | 74007 |
rs45646477 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Btbd11 | Mm_Celera | 10:85525285 | ATTGACAAACAGAGA[A/T]TGGCACAGAAATGGC | 74007 |
rs45652571 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85542150 | ACCTTGGAAGGAGGA[C/T]CCTCACTGAATCCAG | 74007 |
rs45655998 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Btbd11 | Mm_Celera | 10:85546403 | GATGAATGGAAAAGT[A/G]ACTAGTTGTCTTGCC | 74007 |
rs45659816 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85492250 | AAAGACAGTTATCCC[A/G]TGCCCACGGAGTGCT | 74007 |
rs45662948 | snp | C/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85442971 | CATTCCTCCAGTCTC[C/T]CCTCCTTTAGGTCTC | 74007 |
rs45667086 | snp | C/T | | | intron-variant | Btbd11 | GRCm38.p3 | 10:85545783 | TATAGAAATCCTAGC[C/T]CCAACCCCATATACA | 74007 |
rs45670473 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Btbd11 | Mm_Celera | 10:85452453 | AGAGAGCCAGGGGAC[A/G]GGAGCTAACCATTGG | 74007 |
rs45675315 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85471363 | ATAGTCCCTCTCTTT[A/G]TTCTTACAGTGGTGG | 74007 |
rs45675890 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Btbd11 | GRCm38.p3 | 10:85449999 | GCCTTCAGGCAAATG[A/C]CCCTCCAAAGTCAGA | 74007 |
rs45684170 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85512524 | TGGAGGTTTTGGTGT[C/T]CTTAAAAGTCACCCA | 74007 |
rs45687217 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Btbd11 | Mm_Celera | 10:85561650 | CTTCATGCACTGCCC[A/G]CAGATGGAGTGGGAG | 74007 |
rs45691375 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Btbd11 | Mm_Celera | 10:85574680 | CTTGTTCCTCAGTTA[A/C]TGCATCGGATGTCTG | 74007 |
rs45699873 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85556148 | GCCTCGGTTTTGCAT[C/G]TCAGCTGTATGGCCC | 74007 |
rs45699991 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85456773 | TTAGAACTCAACCTC[A/C]GCTCTCGCCGTGCCC | 74007 |
rs45700555 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Btbd11 | Mm_Celera | 10:85524411 | TGTTAGGGGATGATG[A/G]AAATGCCGTGTAATC | 74007 |
rs45703648 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85529321 | ACCCGGCTCTGCTGA[C/T]AGCAGCTGGTGGGGT | 74007 |
rs45704291 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85515611 | GACCCAAAGGGCACC[A/G]GTATTTTCTCACTGG | 74007 |
rs45707741 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85493018 | TGAAGAGGTAGCACA[C/T]AACACATTTGGTATG | 74007 |
rs45709594 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85552942 | GCCCTCATTGGACTG[G/T]GTGATCTTTTTCCAG | 74007 |
rs45710438 | snp | C/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85563393 | AGACATGAAATGATT[C/T]CACACAGATCTAGCT | 74007 |
rs45717410 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85644464 | TATTTGGTGAGTCAA[A/G]CCAGAGAACCGAATG | 74007 |
rs45717886 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85514454 | TGTTAACCCAGCTTG[C/G]CAACAGGCTCTGGGG | 74007 |
rs45723470 | snp | C/T | 0.277778 | 0.248452 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85592597 | TGCTGCTGCCACCAT[C/T]GCCTCCGCTGCTGCT | 74007 |
rs45728889 | snp | G/T | 0.260355 | 0.249785 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85592333 | TGCTATAGAAACCAA[G/T]TTATGCCCCTTGAGC | 74007 |
rs45733624 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Btbd11 | Mm_Celera | 10:85642892 | CTGCTTCCCATGGCC[A/G]CCGAGGGAAGAGAAT | 74007 |
rs45739241 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85397354 | AATCATGTCACGTAC[A/G]TTAAGCTACCTCATT | 74007 |
rs45740681 | snp | A/C/G | 0.5 | 0 | intron-variant | Btbd11 | GRCm38.p3 | 10:85522199 | TCCCAGCCCAGGGGG[A/C/G]ATTATTCCTGCAGGG | 74007 |
rs45741239 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85465670 | TTGGAAATCCTCTCC[A/G]TCAATGGAACAATCT | 74007 |
rs45748195 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85443567 | ACCCTTCAAAACTGG[C/T]AGCCCTGATGTTCTG | 74007 |
rs45749775 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85539449 | GGAAGAGAGGATGGA[A/G]ATGCAGTGTGAGATC | 74007 |
rs45751393 | snp | C/T | | | intron-variant | Btbd11 | GRCm38.p3 | 10:85389245 | GTTATCAGCTACAGG[C/T]ACCCTTTTTCTGGAG | 74007 |
rs45753608 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85518482 | CTGGTTCACAGCTAG[C/T]ACAGGAGAGTTCCAA | 74007 |
rs45763435 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85646555 | AAAATGAACCTTCCA[C/T]GTGGGTTTTTGATTG | 74007 |
rs45764505 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Btbd11 | Mm_Celera | 10:85641859 | TAGATCCGATGAGAT[G/T]CAATACCTCTGGCCT | 74007 |
rs45770287 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Btbd11 | Mm_Celera | 10:85608887 | CTAGGGCTCCAGATC[C/T]GGGCTGTCGGTTAGG | 74007 |
rs45778450 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85626950 | TGGTTGTAAAGACAC[A/G]CATAGGTTTGTTGTA | 74007 |
rs45780799 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85604607 | CTGGGCCTTGGCTCT[C/G]GGTGGCCTGGAACAC | 74007 |
rs45794942 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85490286 | GAGAGATGCAAGCCA[C/T]GATGAGAGCCAAGCT | 74007 |
rs45796294 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Btbd11 | Mm_Celera | 10:85635674 | CAGAGCATCTGGGAG[A/C]CTTGGGGCCAGAGCA | 74007 |
rs45797110 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85478843 | AGATAAGGCCCCGCT[A/G]GCTACTGAAGTCCTC | 74007 |
rs45799378 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Btbd11 | Mm_Celera | 10:85525618 | ATTTAGAGGCAGAAT[A/T]TGGAGGAATCTCTCT | 74007 |
rs45801766 | snp | C/T | 0.165289 | 0.235211 | intron-variant, upstream-variant-2KB | Btbd11, LOC105245252 | Mm_Celera | 10:85594612 | CTTTCATTCCCTGGC[C/T]CTCACCTTGTCACCT | 74007 |
rs45802575 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Btbd11 | Mm_Celera | 10:85607706 | AATTACAAGGCTCCT[A/G]AGCCTGACTCGGGTT | 74007 |
rs45805699 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85461356 | TCCATTGACAGACAT[A/G]TGTGCATCTTTTCAT | 74007 |
rs45805789 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85459114 | CTGCCATTGCCATCC[A/T]TCCTGCAGAAGTGCC | 74007 |
rs45809891 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85432902 | GCCACACCTCCAAAT[A/G]GTGCCACTCCCTGGG | 74007 |
rs45810519 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85469105 | CTGAACTAATGGTAA[C/G]TATACAGTGTGCCAG | 74007 |
rs45813944 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85458416 | GAGTTAAGCTCACGT[C/T]CAAAACCTCTGCAGA | 74007 |
rs45815379 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Btbd11 | Mm_Celera | 10:85538001 | TTCCTTCACTAAAGA[C/T]ATGGGGGAACTGGAA | 74007 |
rs45820351 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85644436 | AAACTAAGGGGAATA[C/T]GTAGGAGCCTTGTAT | 74007 |
rs45823655 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85453428 | CCCAGGGCCCTAGGT[A/G]CTGTCATCCTAACTC | 74007 |
rs45824927 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85540280 | TAAGATCTCTGAAAA[A/G]GAAACTCGTGCTTGG | 74007 |
rs45830882 | snp | A/G | | | intron-variant | Btbd11 | GRCm38.p3 | 10:85545787 | GAAATCCTAGCCCCA[A/G]CCCCATATACATCAC | 74007 |
rs45836916 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85606666 | AGGTGTCTTCCAGGA[A/G]GGGAATTTGCAGCAG | 74007 |
rs45841645 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85530136 | ACTCTGTGCCAAGAT[C/T]GTTTCTCTGCCTCTG | 74007 |
rs45847793 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Btbd11 | GRCm38.p3 | 10:85522303 | TATAAGGCAATATTT[C/T]CAAGACCATACAAAA | 74007 |
rs45848321 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85451223 | CTTCCATAACCCCAG[C/T]TCAGCCCAGTGAGTT | 74007 |
rs45848990 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85438812 | CCACCTTCCTAAGGG[A/G]TTGGAATGGCAACTC | 74007 |
rs45850961 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85503654 | TCTGTGGCCACATCC[A/C]GCTCTGCTCTGTGCG | 74007 |
rs45851068 | snp | C/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85438795 | AAATCACATGGCCAT[C/T]CCCACCTTCCTAAGG | 74007 |
rs45852252 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85613816 | GTATGACTTCCTTCA[A/G]CACAAAGAGCCATTG | 74007 |
rs45855590 | snp | C/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85536712 | GAACAGTGTGGATGT[C/T]GCATTGCTCTGAGCT | 74007 |
rs45864792 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85504451 | TCTGCTGTCACACCC[A/G]TATTCTAGCCAGGGT | 74007 |
rs45865522 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85640111 | GTGGGACACAGTCAC[A/G]GGACCACAAGGGCTT | 74007 |
rs45867707 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85419639 | AATTCTGTGGTTGGA[A/G]GTCACCACAACCTGA | 74007 |
rs45870708 | snp | A/C | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Btbd11 | Mm_Celera | 10:85596963 | CCTTGCCTCAGTGAC[A/C]TCCAGGCCCTGACAA | 74007 |
rs45878710 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85652796 | CTTTGGCCAAGGAGA[A/G]AGTTGTAGGGCTCTG | 74007 |
rs45879910 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85628082 | CACCAATCAACTGCC[C/T]GGAAACCTTTTAGCT | 74007 |
rs45881195 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85398748 | TAGGAGGGAGAGTCC[A/G]TGATTCAATCTGTGT | 74007 |
rs45886837 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85507841 | CTTTTCATTACAATT[A/G]CTTGCATAAGTTTGG | 74007 |
rs45890000 | snp | A/C | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85490391 | AAGCAGTGAAACATG[A/C]AGTTGTAGCATTCAC | 74007 |
rs45891062 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85486488 | GGAAAGTGCTTACAT[C/T]TCTCCCGGGTATCTC | 74007 |
rs45892608 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85445654 | TGACCTTCAGATGGC[A/G]GGCTCTGTTTTGATT | 74007 |
rs45893458 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Btbd11 | Mm_Celera | 10:85525129 | CTCAGATCTGCATGA[C/T]TATTCATCTGAGTAA | 74007 |
rs45896213 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85630535 | TTCTGCAGCTTTTGT[C/T]CCATTACCGGATCTT | 74007 |
rs45910154 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85517424 | CCCTGAGCCCAGTCC[A/G]CCCCAGCTCTGTCCT | 74007 |
rs45913524 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85656340 | TCCTCTGTGCTTCAG[A/G]GAAGTACTTGAGACA | 74007 |
rs45924030 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85624263 | CACATGCTTCTCTGG[C/T]TCAAATCCAAGCTAT | 74007 |
rs45929186 | snp | G/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85657173 | TTGGTTGTGCGGAGA[G/T]GATAAGAAGGTGCTG | 74007 |
rs45936322 | snp | G/T | | | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85586927 | CTAAGAGTATCTGTT[G/T]CTCTTATGGGAGACC | 74007 |
rs45936754 | snp | A/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85423228 | CTCAGAATTCAAAAC[A/T]CAATTCAGCTCCCGT | 74007 |
rs45943184 | snp | A/G | | | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85587024 | CAAGGACCTCTTCTG[A/G]GTTTGTAGTACCAGG | 74007 |
rs45945079 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85482386 | GGAAGAGGCGGGGCA[C/T]GCCTAGTGCAGTAGT | 74007 |
rs45948922 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85650009 | TACCAGGCAGCTGGA[C/T]GCAGAAACCCCAAGT | 74007 |
rs45957230 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85451487 | TGAGAGTAGGAATTT[A/G]TAGAAGACAGGGTCT | 74007 |
rs45958450 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85642718 | ATTGACCATCAAGGT[A/G]ACAGGTTGGAAAGGC | 74007 |
rs45959604 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85534887 | TAATGACTCACAGGG[A/G]CTCAGGGAGGAAGAT | 74007 |
rs45963287 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85458095 | CAAAACATCCAACAA[C/T]CTTAAAATTCAGGTT | 74007 |
rs45971938 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85557617 | GATAGGCACTGAGTC[A/G]GGAACAGAAGTTAGT | 74007 |
rs45972362 | snp | A/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85635578 | CCCTAAATTTATCTC[A/T]ATTTAACAAACAGGA | 74007 |
rs45972593 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85614052 | TCACACTCATGGAAT[C/T]CTGGGATGGGAAGCT | 74007 |
rs45974378 | snp | A/C/T | 0.152778 | 0.230321 | intron-variant | Btbd11 | GRCm38.p3 | 10:85546385 | GTTTGGCACCTCTCG[A/C/T]TTGATGAATGGAAAA | 74007 |
rs45982075 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85584826 | TAATGGCTGGGTGCT[A/G]GATTGCACAGGCGTG | 74007 |
rs45982309 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Btbd11 | Mm_Celera | 10:85546063 | ATATAACGCCCAGAC[A/G]AAAGCTCGCATGGCT | 74007 |
rs45984600 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Btbd11 | Mm_Celera | 10:85459560 | TGGTTTAATTGATCT[A/T]TTTTTTTTTCAATTA | 74007 |
rs45986819 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85540156 | CACGCCCTTCCTTAA[A/G]CAGGTTTTAGACTCC | 74007 |
rs45989421 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85477549 | TAAGGGACCCCCACG[A/G]ATCAGTTCAATTTCA | 74007 |
rs45994290 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85547366 | GTCAAGAGCCCCCAA[A/G]CCCATAACAGTCCCC | 74007 |
rs45998143 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85543323 | AACAAATACTTGACC[A/G]GCTGAACCATCTCTC | 74007 |
rs45998931 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85463524 | TCTCCCTCCGTCTCA[C/T]CTGAGCTGCCACAGT | 74007 |
rs46004565 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85448270 | CTGCAGAGCCCTGTG[A/G]CTTGAGTCATTGGAC | 74007 |
rs46007301 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85398609 | CCCGTGTCTGAGCCT[A/G]CTTCAGTGCCTCCAA | 74007 |
rs46010998 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85607975 | GTTGGTTTTCTTCTC[A/C]TTTTAGGGCTAAGAC | 74007 |
rs46012648 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85639951 | CGTGGGCAGCTGGAG[C/G]TCGCAAGCACAGGAC | 74007 |
rs46015734 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Btbd11 | Mm_Celera | 10:85526945 | CCAGGAAGCCAGGTG[A/G]CCCAGCTATCAAATG | 74007 |
rs46022133 | snp | A/G/T | | | intron-variant | Btbd11, LOC105245252 | GRCm38.p3 | 10:85588254 | TCTTCCACAGCCTGG[A/G/T]GATAACGATATAAAG | 74007 |
rs46022444 | snp | A/C | | | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85591269 | CCCGAAAAAGACAGA[A/C]AAGCAGAGAGAAGTG | 74007 |
rs46031004 | snp | C/T | | | intron-variant | Btbd11 | GRCm38.p3 | 10:85414173 | CTGTATGGCCAGGGA[C/T]GTAGCTCAGGGGTAG | 74007 |
rs46031883 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85474758 | GAACAGTGGTGCCAA[C/T]CTGCCAGAGCTTCAT | 74007 |
rs46035085 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Btbd11 | Mm_Celera | 10:85642605 | CTAAAAATGGAAACA[C/T]TGGCGGCAGAGTCAA | 74007 |
rs46039789 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85622924 | ACACACGCATGCACG[C/T]GTACTTTAGACTAAC | 74007 |
rs46042387 | snp | A/C | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85442219 | TCAGACTTCTACACG[A/C]TCCTGATCAGAACTG | 74007 |
rs46042929 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Btbd11 | Mm_Celera | 10:85444181 | CATCATAGGCTTTGC[A/G]CCCTCCTGTAAATTC | 74007 |
rs46044101 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Btbd11 | Mm_Celera | 10:85596884 | GGGAGCAGATGCCTC[A/G]TAATCACCTTTTACG | 74007 |
rs46045847 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Btbd11 | Mm_Celera | 10:85658542 | GAAGAACCGTCCACG[C/T]GTCTGCAGGTTAGAT | 74007 |
rs46048525 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Btbd11 | Mm_Celera | 10:85624379 | TGGGACCCGAATGTA[A/T]CAACTCAGATAAAAC | 74007 |
rs46052658 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85530811 | TCCTCCAGGCAAGAG[A/G]GAGCCACTACAGGTT | 74007 |
rs46054392 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85538098 | ATACAGTGGAGGCAG[A/G]ACCCTAGGACAGAAG | 74007 |
rs46056765 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85583917 | CTGCGGCCATGTTGA[C/T]TATGTATTCTGTGCC | 74007 |
rs46063542 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Btbd11 | GRCm38.p3 | 10:85545529 | GCACTTTTCAGGCTC[C/T]GAGTCTGTCTTCTCT | 74007 |
rs46066350 | snp | A/C | | | intron-variant | Btbd11 | Mm_Celera | 10:85488286 | AACAAGGCCACACCT[A/C]CTAATCCCTGTCAAG | 74007 |
rs46068898 | snp | C/T | 0.165289 | 0.235211 | intron-variant, upstream-variant-2KB | Btbd11, LOC105245252 | Mm_Celera | 10:85594960 | GCAAAGCTTGGGAGC[C/T]GTGGAAGATGTCACT | 74007 |
rs46071402 | snp | A/G | 0.18 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85526958 | TGGCCCAGCTATCAA[A/G]TGCCAGGAACCAAGA | 74007 |
rs46080176 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85475273 | CACTGTAATTGTGCT[G/T]CGAGGAGGTTTCCTC | 74007 |
rs46085137 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85479252 | ATACCATAGGCTACT[A/G]TCTTTCCTCATGGGT | 74007 |
rs46086293 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85501292 | TGAGGCTGTACCTTG[C/T]CCATCTCCCTTTCCC | 74007 |
rs46091984 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Btbd11 | Mm_Celera | 10:85537058 | ATTCTCTCTTTATCC[A/G]TGAAGCCTTTCTTGG | 74007 |
rs46099986 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85553451 | GAAGCACTTATAGAG[C/T]GAATAGTTTCAAGCA | 74007 |
rs46104524 | snp | C/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85397671 | CCAGTGACTAGTATT[C/T]TTACACGTGGTCTTA | 74007 |
rs46113300 | snp | C/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85389928 | CCAAAGCCCATCCCC[C/T]ACCCACCCCTCTGTT | 74007 |
rs46115244 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85604743 | TGCAGCACTGGCAGG[C/T]TAAGTCCCTTCTTCA | 74007 |
rs46116320 | snp | A/G | 0.18 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85563980 | TCTAAAGAGGCCCAC[A/G]AGGAAATGCAGAACT | 74007 |
rs46118347 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85494154 | AAGAGTAGAGAAGAC[C/T]GTGGACATGATTTTC | 74007 |
rs46118626 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85393303 | CCCAGCATTAGCTGG[A/G]CGGGGCTTGGGTTTC | 74007 |
rs46119461 | snp | C/T | | | intron-variant | Btbd11 | GRCm38.p3 | 10:85534911 | GGAAGATCAACTTTA[C/T]TCGGGGTGAATCAAG | 74007 |
rs46122487 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85467959 | TTGGTGGTCACTTGG[G/T]CACGTTCCAAGTGAT | 74007 |
rs46128726 | snp | G/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85498968 | TAGGGACCAAACTCA[G/T]GTCCCTGGACTTGTA | 74007 |
rs46135513 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85620330 | CTGAACTGCTCTCAC[C/T]GCAGACAGGCAAGGC | 74007 |
rs46140739 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Btbd11 | Mm_Celera | 10:85612799 | ATAGGATATATATTC[A/G]TTATCTACAAGAGAG | 74007 |
rs46144127 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85587455 | AAGGGCTGGCCTTTG[C/T]ACCACGCCACACACA | 74007 |
rs46144634 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85545713 | TGTTTCCAGAGCAAA[A/C]AGGGAGGAAGAGTAG | 74007 |
rs46145141 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Btbd11 | Mm_Celera | 10:85635301 | GAATACCTGGGTCAC[A/G]TGTCACCTCCTGCCC | 74007 |
rs46148128 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85455819 | GCATGAACAGGGACA[C/T]GCCTCAGGGCGTCAC | 74007 |
rs46153099 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B | Btbd11 | Mm_Celera | 10:85660486 | GGGGTGATTCTCCAG[A/G]TTTCCTTTCCTTAGG | 74007 |
rs46154023 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85514020 | AAGCCAAATAATAAG[A/G]TTTATTTAAGGGCCT | 74007 |
rs46156449 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85646646 | GTAGCTGTGGCCCTG[C/G]AGGTTTTAGTCCTGA | 74007 |
rs46156743 | snp | C/T | | | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85588881 | CAACCCCATCCTTCA[C/T]CCCACTCCCGTGATT | 74007 |
rs46164207 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85603799 | TACAGGTTTGTGTAT[A/G]GTGTGCCGTGCTGAT | 74007 |
rs46165871 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85533289 | CCCTAAGGGGCTTCG[C/T]GATGCATAGAAATAA | 74007 |
rs46169454 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85474163 | TTCAAGCAGGCCCCG[C/G]TGAAAATTGGAAAAG | 74007 |
rs46172277 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85651588 | TGGGGTCTTGCTCAC[A/G]GTGTCTTATTCCTTC | 74007 |
rs46174026 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85520309 | TTTCTGGCTTCCTGA[A/G]GAAGGGCCACCATCT | 74007 |
rs46177399 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85451553 | TTCTCTACCATCTCT[C/T]GGACACCTTACTCAT | 74007 |
rs46182886 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Btbd11 | Mm_Celera | 10:85628564 | GTGCTTTCAGTTACA[C/T]GAGAGCCCTTGTCAA | 74007 |
rs46184409 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85543592 | CATTGTTAGGAGGTG[A/T]GTCCTTGGTATGGCC | 74007 |
rs46185678 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85532347 | TCCATGTGGTCAGCT[G/T]TAGGGTATTTAGGGT | 74007 |
rs46187950 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85628408 | CCAGAAAACACCACG[C/T]GCTGGTGCTAATATC | 74007 |
rs46192100 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85653748 | CATCAGAGTAGAGAT[A/C]CAGGGAACACAGGCA | 74007 |
rs46192949 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85556077 | AAGACTCAGGCACTA[A/G]CAAGAGACGGAACCT | 74007 |
rs46206741 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85458996 | ATTTTTTTTTCACCC[C/T]ACATTGTTTTGCAAG | 74007 |
rs46213515 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85604828 | GCCACTGCCTCCCAC[A/G]TGCTGATGCCAACGC | 74007 |
rs46220303 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85528045 | GACCAGCCTGAACCT[A/G]CCCTGGAAGTGATAG | 74007 |
rs46224367 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85611140 | CATCATGACCAAGAA[A/G]CAAGTTGGGGAGGAA | 74007 |
rs46237028 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Btbd11 | Mm_Celera | 10:85642255 | ACTACTACAGGCAGG[A/G]CAGAATGGAAAAGAC | 74007 |
rs46237582 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85585311 | TGTCGCCCAAGAAAC[C/T]AAGGACATTTTCTTC | 74007 |
rs46240944 | snp | C/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85407337 | CCTCTGGAAGAGCAG[C/T]CAGTGCTCTTAACCC | 74007 |
rs46241098 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85629481 | TTATACTGAAGCATC[C/T]ATTTGGCCAAGCATT | 74007 |
rs46243353 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85549459 | TAGCTGCTTTCCTGG[C/T]CTCTGTGCTGAGAGG | 74007 |
rs46243512 | snp | G/T | 0.426035 | 0.177515 | intron-variant | Btbd11 | GRCm38.p3 | 10:85545945 | GCTTGGGCTGTCTCT[G/T]GAAGAAAGAACGAGG | 74007 |
rs46243956 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85506320 | CTGGCAGCAGGTAGT[A/G]TGGCACTCTGAATGA | 74007 |
rs46245460 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85607244 | CCCTGGGTTTGTTGT[G/T]GAAAGTGTTGTTTAT | 74007 |
rs46245765 | snp | C/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85643932 | CCAAGCAGTTCATAA[C/T]GTGTATGTATGTGCA | 74007 |
rs46248459 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85443821 | AAGAAGGGTGACCCT[A/G]CAGCTAGCATCCTTC | 74007 |
rs46259812 | snp | G/T | 0.473373 | 0.11227 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85590658 | CCCACACTTCCTCCA[G/T]ACCTCAGACACTCAT | 74007 |
rs46266344 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Btbd11 | Mm_Celera | 10:85546071 | CCCAGACGAAAGCTC[A/G]CATGGCTGGTTAATT | 74007 |
rs46270744 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85393277 | CAGCATCATCTGGGC[A/G]GGGCTTGGGTCCCAG | 74007 |
rs46274636 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85604841 | ACGTGCTGATGCCAA[C/T]GCTTTCGCGCCTCTG | 74007 |
rs46276011 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85648227 | AGACAAGAATGCATG[G/T]AAAGGACTTCAATGA | 74007 |
rs46281331 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85482800 | ACCCGCATCACTCTG[C/T]TCTTTGTCTTCCTAT | 74007 |
rs46281561 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85444945 | GCCAACCTGACATGC[A/G]CTAAATGTGTGAGAC | 74007 |
rs46295956 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85553476 | CAAGCAGAGGTAGTG[A/G]TGGTCTCACATAGAC | 74007 |
rs46298404 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85503336 | AGCACATACCTCACC[C/T]GAGAAAGCATCTTTG | 74007 |
rs46298532 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85455830 | GACACGCCTCAGGGC[A/G]TCACATGCAGATCAC | 74007 |
rs46301710 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85489591 | AGATGCTCACAGATA[C/T]TGATTCTAGGGTCAC | 74007 |
rs46302959 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85443323 | GTTACCTCTGGTTGA[A/G]AACCACTGTCCTGGG | 74007 |
rs46306299 | snp | C/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85577014 | CACATCCTTCGAAGG[C/T]CCACTCCACAGCACA | 74007 |
rs46309129 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85498130 | GTGTGGAATTTTCCA[C/T]AGCAGCAAAAAGGAT | 74007 |
rs46312344 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85509031 | ATAAGAAGACTAGGT[A/G]CAAATGCAATTTTCT | 74007 |
rs46314267 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85457157 | TGATTGAAGCCCAGG[C/T]AAGCCATATATACAC | 74007 |
rs46322580 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85554774 | GTCTCTGTCATTACT[A/G]GCACCACTCCCATTT | 74007 |
rs46326530 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85647675 | GGGTAAGCCACAGGG[A/G]CATGGATGAGTCTTT | 74007 |
rs46326698 | snp | C/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85534913 | AAGATCAACTTTATT[C/T]GGGGTGAATCAAGGG | 74007 |
rs46326828 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85624183 | TCAGTCAAGTGAACA[A/G]GAAAGCAGTAGGTTC | 74007 |
rs46329440 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85515691 | AATGGTCAACTGTGA[A/G]TATATACTGATCCAT | 74007 |
rs46349512 | snp | C/T | 0.18 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85481447 | TTTCTCTCTTGCCTC[C/T]CTGCCTGCCTGCTCC | 74007 |
rs46351054 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85606777 | GCAATGAAGACCTCA[C/T]GTCCAAGACCAAGGT | 74007 |
rs46357046 | snp | C/T | 0.260355 | 0.249785 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | GRCm38.p3 | 10:85591885 | TCCTGGACCTCAGAT[C/T]CCCTCTGAAGCGTTT | 74007 |
rs46359719 | snp | A/T | | | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85588867 | AAGTCCAGTATCACC[A/T]ACCCCATCCTTCATC | 74007 |
rs46365533 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85503185 | ACCCCCACAGCTCTG[C/T]TTTTTCCTGGGAATG | 74007 |
rs46370615 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85581533 | TCACAATTTTCTATC[C/T]GAGCTGGGTATTTGG | 74007 |
rs46376261 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85640334 | GTAGACAGTGAGCTC[A/G]TAGAGCAAGCAGGTC | 74007 |
rs46377114 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Btbd11 | Mm_Celera | 10:85607891 | AGCAGAAGCTAGGGG[A/G]ACAACTAAGAGGCAG | 74007 |
rs46386105 | snp | A/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85441242 | TAGGATGATCTGATT[A/T]TGACTGGAAACACCT | 74007 |
rs46386701 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd11 | GRCm38.p3 | 10:85522319 | CAAGACCATACAAAA[C/T]GATGGTGGAAATTAT | 74007 |
rs46387613 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85651033 | CCAGTCACATGGAAG[A/G]CAGTTGAAAATGGAG | 74007 |
rs46387970 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85644884 | GTGTGCAGGATGTCA[C/T]AGTTCATCTCAGCTG | 74007 |
rs46392063 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85476558 | ATCAAGCTTCTTTGT[C/T]CTTCTTTTGTGCTTT | 74007 |
rs46393499 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85514747 | ATGAGAACACAGCAA[C/T]GGAGACACAAGGGAG | 74007 |
rs46398406 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85485697 | TTTCAAATATTAAGG[C/G]AGATTTTTAAAAGTC | 74007 |
rs46398920 | snp | A/C | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85649794 | GTGTGGGCGGTGGGC[A/C]TTACAGTGGTGTTTC | 74007 |
rs46403214 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85504980 | GCTAGCTCCAGAGGC[A/T]CCAGATGTGTCTACC | 74007 |
rs46403987 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85465471 | CAGGATGCTCAGGCG[A/G]TATGGGGAACTTCTC | 74007 |
rs46404216 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85589728 | TCAACTACAATTCTA[A/G]CAAAGGAAGAACTAA | 74007 |
rs46407116 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85509816 | ACTACGATGCCTCCT[A/C]TAGAAAGGGATACCT | 74007 |
rs46411450 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85485445 | TGTTGGAACAAAGCA[C/T]GCTGGAAAAGGCAGC | 74007 |
rs46414688 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85608898 | GATCCGGGCTGTCGG[C/T]TAGGAGGGTGACTAG | 74007 |
rs46417126 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85476949 | ATATAAGTTAGAGTC[C/G]TTGAGGGGAGGATGT | 74007 |
rs46417303 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Btbd11 | Mm_Celera | 10:85630096 | GTTGGTTCCTGGCTC[C/T]GGGGAATCCTTGTGA | 74007 |
rs46421360 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85441916 | GGAGTTCTGGGATTA[A/C]AGGTATTTGTCACAA | 74007 |
rs46421645 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85438654 | GGGGCTCTTGGAGCC[A/G]CCACCATCATCATGG | 74007 |
rs46424095 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85602786 | CAGTCAGTAAGGATC[A/G]GCCTCGTCCAGGATT | 74007 |
rs46426384 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85581421 | TGAAGCCTTAGGTAG[A/G]CTTCAATTTTTAGAA | 74007 |
rs46427202 | snp | A/G | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85590807 | GAGAAGAGGATAATC[A/G]GATAGATACATGAGA | 74007 |
rs46436750 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85514626 | AAATATATATAAAGA[C/T]TTAACCCTCAGTAGT | 74007 |
rs46445418 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85504577 | TCTTGTCCTTGGCAC[A/G]TGAACCAGGATCCTC | 74007 |
rs46448970 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Btbd11 | Mm_Celera | 10:85546730 | TGCTTGCTGTGTACA[C/T]AAAGCAGTGCCAGTG | 74007 |
rs46460070 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85541932 | ATAAAAAACAGAGGA[A/C]GGTGGGGCACTCTGT | 74007 |
rs46462569 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85604878 | CAAAATGCTGCCCTC[C/T]TTCTGGTCCTAAGGG | 74007 |
rs46466311 | snp | G/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85444901 | TAAGGGCTATATCAC[G/T]CAATGTATCAAGGGT | 74007 |
rs46475595 | snp | C/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85502320 | CTGAGGTTGGGGATC[C/T]CGGGTGGGATCAAAT | 74007 |
rs46478370 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85649478 | GCCCCCACTGAGGCC[A/G]CAGCTGGAGCTAGGC | 74007 |
rs46480121 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Btbd11 | Mm_Celera | 10:85607235 | GTAAGATGGCCCTGG[A/G]TTTGTTGTTGAAAGT | 74007 |
rs46489280 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Btbd11 | Mm_Celera | 10:85544615 | GTCCATGTGTTAGAG[A/C]CACAGACATCAGAGA | 74007 |
rs46490266 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85511143 | AAAGAGGTTCATGTA[C/T]ACTGGCTCCCACTCT | 74007 |
rs46492553 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85631913 | CAAGTTGCCCTCCAG[A/G]AAACATGGCCAGCCA | 74007 |
rs46492636 | snp | C/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85575893 | AAGTTCTAACCCTTG[C/T]CCAAGGTCACAGAGC | 74007 |
rs46496091 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85608619 | GAGGTTGCCATGCCA[G/T]CATAGGCCATGCAGA | 74007 |
rs46497428 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85397708 | TGCAAAGGGATTGGG[A/G]ATTATAGCTTCTTGA | 74007 |
rs46498172 | snp | C/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85598999 | TAGGTCGCAGCCACC[C/G]GGGTGTACGTGCACT | 74007 |
rs46502766 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85442425 | TGATCTTCATACCTG[C/T]TTGTTGCATCAATGG | 74007 |
rs46527149 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85486801 | ACATGAGTAAGTCTG[A/G]TCTATATAGCCAGAC | 74007 |
rs46530447 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85481813 | CCTGCCACGGTGGCC[A/C]TATTTCCATCACTTG | 74007 |
rs46535999 | snp | G/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85614431 | TGCCTCCAGTTTCCA[G/T]ACCTTAGGGAGAGGC | 74007 |
rs46536003 | snp | G/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85433547 | ATGGCTTCTGCATCA[G/T]CTCTGGCCTTCAGGT | 74007 |
rs46538082 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85502599 | GAGAAACTTACTTCT[C/T]TTTCACTTTCTTGCC | 74007 |
rs46543985 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85614748 | TGCTTAGGAATCCTG[A/G]TAGCATTGAACTCAC | 74007 |
rs46551290 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85606564 | AGCGGAGCGGTATGG[A/G]AGATGTCACCCTTGT | 74007 |
rs46561207 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Btbd11 | Mm_Celera | 10:85655882 | TAAGAGTCCTTAGCA[C/T]GTTCCGTCAGCAGCA | 74007 |
rs46562913 | snp | A/T | 0.152778 | 0.230321 | intron-variant, upstream-variant-2KB | Btbd11, LOC105245252 | Mm_Celera | 10:85594681 | GCTGCTTATGCCCTG[A/T]ACTGGCTCCTTGGGC | 74007 |
rs46564609 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Btbd11 | Mm_Celera | 10:85550185 | TCCTTCTGGGAAATG[C/T]TCTTGTCCCTCAAGC | 74007 |
rs46565827 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85620644 | ATTAATGAATTAAAC[C/T]AGGGGCTGGCAACAT | 74007 |
rs46570051 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85492452 | GTGTAGGAAATCCTC[A/G]AGCCAATTAACATTT | 74007 |
rs46573481 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85487942 | CAATGAGATTATGTT[A/G]GGGAAATCTTCCTCA | 74007 |
rs46574071 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Btbd11 | Mm_Celera | 10:85525257 | CCTGAGAACGCCTGA[A/G]CCCTGGCCTGCCATT | 74007 |
rs46574765 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85488846 | GCAAAGTGGGGTAAG[C/T]ATGTCTAGACAGGCA | 74007 |
rs46576369 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85456134 | TGACTCAACCCAGGT[A/G]GACTCTGCTCCAGGG | 74007 |
rs46584233 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85538998 | CTTGACTTTCTTGCT[C/T]CTCCAGTTAATTCTC | 74007 |
rs46590471 | snp | C/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85393781 | GGAGCCTCTGTAGAG[C/T]AGTTGCTATGATATC | 74007 |
rs46592886 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85556472 | TATTCCTAAAAACAG[C/T]GGGGACAGCAGTTTA | 74007 |
rs46595600 | snp | C/T | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85641398 | GTGGGTGAGTACTTG[C/T]TCACTGTGGGTGAGT | 74007 |
rs46600492 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85510761 | AGGCTGAGCTGTAGG[A/G]TGTTAGAAAGAGGGA | 74007 |
rs46601868 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85504688 | GGCGGTGGTAGTCCT[C/T]CGTTCTGGTGCACAC | 74007 |
rs46603304 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85613735 | GAACTTTGCAAGCAT[C/T]GCATGTTCTATTCGA | 74007 |
rs46604573 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Btbd11 | Mm_Celera | 10:85641990 | GCTCTGGAATCCAGT[A/G]AGGATAACTGATCAC | 74007 |
rs46606260 | snp | C/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85398590 | AAGGCTGGCTCTAGC[C/G]AACCCCGTGTCTGAG | 74007 |
rs46620684 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85544136 | TTAGCACTTGAAAGA[A/C]AGCCTAGCCCATCGG | 74007 |
rs46634237 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Btbd11 | Mm_Celera | 10:85442906 | AGGCCTTGTACACCC[C/T]GCCCAGGGTCTCTGC | 74007 |
rs46635622 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85445069 | TCAACCACCCCTCTT[A/G]TGTTTTAGCTCTTCA | 74007 |
rs46639401 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85471513 | ATACGTGTCTACTGT[C/T]ACAAACTCACACTGA | 74007 |
rs46640104 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85505699 | CCCTTGTTCCATGAA[A/T]TTTTAGAGTGCCTGC | 74007 |
rs46640409 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Btbd11 | Mm_Celera | 10:85527392 | CCATATTCAATTTGC[G/T]CTACTTGCATGAGCA | 74007 |
rs46643156 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Btbd11 | GRCm38.p3 | 10:85538353 | TGCGATTAGACTCTT[C/T]TCTTTTTTTCTTACA | 74007 |
rs46647481 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85587392 | CCAAAAACACATCCT[A/G]GGCTTGTATTGTCCA | 74007 |
rs46650496 | snp | A/C/T | 0.132653 | 0.220748 | intron-variant | Btbd11 | GRCm38.p3 | 10:85473587 | TCCTGAATACTCTTC[A/C/T]GGCTACCTTTGGGCT | 74007 |
rs46651303 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85393092 | GCTTGGCGGGACTTG[A/G]GTCCAGCATCCACTG | 74007 |
rs46651663 | snp | C/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85561474 | AAGATCTCCAGGTTG[C/G]TGTCTTCTGAAATTT | 74007 |
rs46654752 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85476726 | CCTATGACACTGAAA[C/T]GCTATGATGCCTCCT | 74007 |
rs46661737 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85628982 | GCTTTCAGAAAGCTG[C/T]TTCGAATCTCTCCTA | 74007 |
rs46662258 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85640385 | AAACTCAGTGTCTAT[A/G]CTCCAGGAGGACAGT | 74007 |
rs46666859 | snp | C/T | | | intron-variant | Btbd11 | GRCm38.p3 | 10:85541243 | TAATAATAATAATAA[C/T]AACAACAACAGGTTC | 74007 |
rs46670707 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Btbd11 | Mm_Celera | 10:85529257 | AACCAACCTTCGGAC[A/G]TGTGTTTGGGGGATG | 74007 |
rs46673657 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | GRCm38.p3 | 10:85441794 | TCTTCCCTATGTTAC[A/G]GTATTAATAGCATGA | 74007 |
rs46677627 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85448722 | CCTAAAAAGATGAGC[A/G]AGGAGCAAGTAGGCC | 74007 |
rs46681861 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85457607 | CTCTGCTTCCCAGAA[A/G]TGCTCTCTTCATCTG | 74007 |
rs46685372 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Btbd11 | Mm_Celera | 10:85528101 | GAAACCTAAATTGGT[A/G]ACTAAGAACAGACAC | 74007 |
rs46687631 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85481125 | TTAATACTGCTGTGG[C/T]CAGTCCCCTTCTGTG | 74007 |
rs46693394 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Btbd11 | Mm_Celera | 10:85645519 | CAATAAAGAGATGTC[C/T]GACGTGACCTTTCTG | 74007 |
rs46697252 | snp | G/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85567042 | GGCCATTTCAACAGG[G/T]ATTATAATACCTTTT | 74007 |
rs46701677 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85503910 | TCGTCCAGTGCTTCA[C/T]CCTGGATCCTCTGCA | 74007 |
rs46705593 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85467001 | CTGGCCCTGGCCAGC[C/T]TAAGATTCCACCCAA | 74007 |
rs46708951 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85540248 | CTCATTCTGAGGTGC[C/T]CTGGGTCCAATATTT | 74007 |
rs46719932 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Btbd11 | Mm_Celera | 10:85528449 | GTGGCTCAGCCTAAC[C/T]TGAATGCTGAGTCTC | 74007 |
rs46720728 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Btbd11 | Mm_Celera | 10:85659928 | CTGTCAAGGACCCAC[A/G]TCAAGTCTCGTTTCA | 74007 |
rs46721255 | snp | G/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85648961 | AGCACATGTAAATGT[G/T]TGTGTGTGTGTGTGT | 74007 |
rs46723270 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85443306 | TGATAGGTGAGGAAT[A/G]AGTTACCTCTGGTTG | 74007 |
rs46728951 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85494480 | CCAGAAGTGGGCGAG[C/G]AATGGGAAGACGCTC | 74007 |
rs46734861 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Btbd11 | Mm_Celera | 10:85565907 | TGCTTACTTGCCTAA[A/G]TTAAGCCCAGGGGGA | 74007 |
rs46737747 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85583267 | ATTCCAAAACGGAGA[A/G]TGATTTCTGTCTGTC | 74007 |
rs46742028 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85481388 | AGCTTAATTCCAAGC[C/T]TCTAAGCCCTTCCTA | 74007 |
rs46743702 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85618746 | ATAGTGCTTACACAG[A/G]GCAGGACGTGTCTGC | 74007 |
rs46748419 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85607353 | CTTAGAGAAAGCAGA[A/G]TAGAGTGAGTTGGAA | 74007 |
rs46752840 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85622305 | TATTGGTGGATATCA[G/T]TTATACACACTGGAC | 74007 |
rs46788538 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85528726 | CACCACAATTCTGAT[C/T]CCTTTCACGTTTGAT | 74007 |
rs46789932 | snp | A/C | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85489672 | GAAATACAGTCAGTG[A/C]ATACCAGTCATTTCT | 74007 |
rs46796370 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85483361 | CCTTTGCATTATCTA[A/G]TAGTCTTGGTATCCC | 74007 |
rs46797803 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85462352 | CCCAAGAAGCTTTAT[C/G]AAAGGGGCACAGCAT | 74007 |
rs46819490 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85448806 | AAGGGCTTTCAGAAG[A/T]TTCTCCAAGGTTGGT | 74007 |
rs46828461 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85606596 | TGAAATATGCATACA[C/T]GTCTTTGCTACACTT | 74007 |
rs46831345 | snp | C/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85561807 | AATGAAGATAGGTTG[C/T]GGGTGGGGATGGGAG | 74007 |
rs46831630 | snp | A/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85438094 | AGCTAAATGTGTACA[A/T]GAAGAATTTAACATG | 74007 |
rs46839750 | snp | C/T | | | intron-variant | Btbd11 | GRCm38.p3 | 10:85545813 | ATCACTACAGAGAAA[C/T]CCTGAAGCCTTGTCT | 74007 |
rs46842428 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85483722 | TGAGTTTTTCAGCTG[A/G]CAGGCATCATGCTCA | 74007 |
rs46849409 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85604971 | CCAGATGCCAAACTA[A/G]CTACACAGCCTGGCA | 74007 |
rs46850088 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85483311 | TGATGAATCTATCAT[A/G]GGTGCCATACCCTAG | 74007 |
rs46850288 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85450045 | CTACTAGCTCTTGCA[C/T]GTGTGACCTGGCCTG | 74007 |
rs46851014 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85489541 | GTGCTGATCTAAATG[C/T]TCTTATTTGAACGAA | 74007 |
rs46851173 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85463329 | GGTAATTTGTATGTA[A/G]TCATCACTCAGGTGG | 74007 |
rs46851812 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85503300 | ACACATTGAACAAGG[A/G]GCCAAGTGGGTATCA | 74007 |
rs46853899 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Btbd11 | Mm_Celera | 10:85542208 | TCAGGTTTGGTAGGG[C/T]GGTGTCTGTGAAGCT | 74007 |
rs46857658 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Btbd11 | Mm_Celera | 10:85448856 | GGATGGCAGGTGAAG[A/C]CGGGAAGAGTAGAGC | 74007 |
rs46858378 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85483656 | TTCCTGTGTGGACCA[A/C]GGGTAGGAGTGTGCT | 74007 |
rs46868316 | snp | A/G | | | intron-variant | Btbd11 | Mm_Celera | 10:85398624 | ACTTCAGTGCCTCCA[A/G]TGCTAATATTATAGG | 74007 |
rs46869165 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Btbd11 | Mm_Celera | 10:85529145 | GTACGTCTGTGTAAA[C/T]GTTCAGGGTTTATGT | 74007 |
rs46877694 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd11 | Mm_Celera | 10:85445048 | CAGAACTCAGAGGCC[A/G]ACATCTCAACCACCC | 74007 |
rs46877958 | snp | A/C | | | intron-variant | Btbd11 | Mm_Celera | 10:85390331 | CAGGGATTCCCACCC[A/C]CCCCCTTCCCAACCC | 74007 |
rs46882528 | snp | C/T | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Btbd11, LOC105245252 | Mm_Celera | 10:85594528 | CATCTGAATCCACCC[C/T]AGTTGTTAGCCAGAG | 74007 |
rs46887722 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Btbd11, LOC105245252 | Mm_Celera | 10:85583736 | AGAGTTTGTGACAGC[C/T]TTTTAAGTTTTTATT | 74007 |
rs46892761 | snp | C/T | | | intron-variant | Btbd11 | Mm_Celera | 10:85463415 | CACTTAGACTCCTGC[C/T]TGGAAAGGTCTGCAT | 74007 |
rs46896000 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Btbd11 | Mm_Celera | 10:85446155 | GCGCCCTTTGTGCAA[A/T]GCCAATGCCAGGGGC | 74007 |
rs46898136 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85554667 | GAAAACAGGGAGATA[A/G]GGAGACTATGAAGTA | 74007 |
rs46898959 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btbd11 | Mm_Celera | 10:85465837 | ACATTAGTGGGACAG[C/T]GAGAGATGCCCTTTT | 74007 |
rs46899562 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85530848 | GTGGGAGAGGAAGAA[C/G]GTCATGGGCTCAAAG | 74007 |
rs46900701 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Btbd11 | Mm_Celera | 10:85512435 | GAGCTTCCTAGGGCA[C/T]GAGGGCATATTCAAT | 74007 |