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 |