SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3657281 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Asb9 | Mm_Celera | X:164513168 | ACCTCTGTGAAGGCT[G/T]TGAGGACACTGGGCA | 69299 |
rs4136868 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Asb9 | Mm_Celera | X:164513552 | AAGGAACAAGTAACA[C/T]CAGACAGTTGCACCT | 69299 |
rs13484100 | snp | A/G | 0.396694 | 0.202437 | synonymous-codon | Asb9 | Mm_Celera | X:164533536 | TCTCGGAACACCTCT[A/G]TATGTGGCTTGTAAA | 69299 |
rs31026875 | snp | G/T | 0.375 | 0.216506 | intron-variant | Asb9 | Mm_Celera | X:164509681 | CTTAAGTTTAAAAGC[G/T]TACATTTAAAAGTTG | 69299 |
rs31027228 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Asb9 | Mm_Celera | X:164514163 | ATACAGTTCTGTTTA[A/G]ATTTTATTACAAGCC | 69299 |
rs31041269 | snp | A/G | 0.5 | 0 | intron-variant | Asb9 | Mm_Celera | X:164499506 | TATACATGTATACAT[A/G]TATACATACATACAT | 69299 |
rs31070478 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb9 | Mm_Celera | X:164505793 | GCATGAACTTGCAGC[A/G]CCCCCACCCTCAATT | 69299 |
rs31090740 | snp | A/G | 0.375 | 0.216506 | intron-variant | Asb9 | Mm_Celera | X:164509720 | TCCTTTTGTGTGCGT[A/G]TGTGTGCCTCTACCT | 69299 |
rs31091928 | snp | C/G | 0.5 | 0 | intron-variant | Asb9 | Mm_Celera | X:164534995 | GATGTTGTTCCCCTG[C/G]AGCCATCCAGTTTGA | 69299 |
rs31103288 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb9 | Mm_Celera | X:164504283 | GTGGCTTTCTCCGCT[C/T]TGGAGAGAAACAGCA | 69299 |
rs31121093 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Asb9 | Mm_Celera | X:164507449 | GAAAGTAGACAATAC[A/G]AAATGCCTTCCCTCA | 69299 |
rs31128113 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Asb9 | Mm_Celera | X:164531764 | TATTTAGGGGTTTCA[C/T]CCAGTCCTTCAAGGA | 69299 |
rs31162720 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Asb9 | Mm_Celera | X:164531513 | CATACAGTGAAAGTG[A/G]AAGGATTAAGCTTGA | 69299 |
rs31166743 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Asb9 | Mm_Celera | X:164505522 | AACCCAGGGATGGTA[A/G]CAACACCAGCGATTG | 69299 |
rs31191248 | snp | A/G | 0.5 | 0 | intron-variant | Asb9 | GRCm38.p3 | X:164532253 | GAGGAGAGAGAGGGG[A/G]GGAAAGAGAGAGAGG | 69299 |
rs31201825 | snp | A/T | 0.5 | 0 | intron-variant | Asb9 | Mm_Celera | X:164499110 | GTCCTGACTTTTTTT[A/T]ATGATGAACAGTGAT | 69299 |
rs31204298 | snp | A/T | 0.375 | 0.216506 | intron-variant | Asb9 | Mm_Celera | X:164512215 | AGCTTGGAGCAGTGC[A/T]TCGCGTAGAGTTTCA | 69299 |
rs31205595 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Asb9 | Mm_Celera | X:164513652 | CCGTAGTAGCTTCTC[A/G]CATCTGTTTGTTCTG | 69299 |
rs31216263 | snp | C/T | 0.5 | 0 | intron-variant | Asb9 | Mm_Celera | X:164534286 | CAGGGCAGGGCCATA[C/T]TTGGCATCTCTCACA | 69299 |
rs31218874 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb9 | Mm_Celera | X:164509719 | TTCCTTTTGTGTGCG[C/T]ATGTGTGCCTCTACC | 69299 |
rs31253848 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb9 | Mm_Celera | X:164512219 | TGGAGCAGTGCATCG[C/T]GTAGAGTTTCATTTA | 69299 |
rs31325209 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Asb9 | Mm_Celera | X:164532937 | TCCACTTCTGTGTTT[G/T]CCAGGCACTGGCATA | 69299 |
rs31340837 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb9 | Mm_Celera | X:164498437 | ATATATATGTATGTG[C/T]ACTACATGTGTGCCT | 69299 |
rs31357485 | snp | C/T | 0.5 | 0 | intron-variant | Asb9 | Mm_Celera | X:164499495 | ATGTATATATGTATA[C/T]ATGTATACATATATA | 69299 |
rs31397381 | snp | A/G/T | 0.5 | 0 | intron-variant | Asb9 | GRCm38.p3 | X:164538240 | TTTCTGGAGTGGGAC[A/G/T]CAGCTTCATATAAAC | 69299 |
rs31453946 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb9 | Mm_Celera | X:164501575 | TCTCTCACACCTTTC[C/T]CAAGAGCACAGAGAT | 69299 |
rs31453949 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Asb9 | Mm_Celera | X:164501619 | ACAGTGCAGCAATGA[C/T]AGGGTGGAGGTGAGA | 69299 |
rs31453952 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Asb9 | Mm_Celera | X:164501693 | ACAACTGGGCCACCG[A/G]TGCCTTTCTCATCTT | 69299 |
rs31454386 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb9 | Mm_Celera | X:164526454 | CTGTGTGTGGCCATG[A/G]GCTGAGCAGAGTTGA | 69299 |
rs31454389 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Asb9 | Mm_Celera | X:164528049 | AACAAGTATCCCCAG[A/T]GGGTGATGGATCCTA | 69299 |
rs31454392 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Asb9 | Mm_Celera | X:164528088 | CATATAGACATTGTG[A/C]TTTTCCAGATTTCAA | 69299 |
rs31454395 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Asb9 | Mm_Celera | X:164510696 | TAGCAGGAATCTTCT[C/T]CAGTGATTGAGTATT | 69299 |
rs31454398 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Asb9 | Mm_Celera | X:164510724 | ATTTGTTCATGCCCC[C/T]GAATGCACCTTTTTC | 69299 |
rs31454401 | snp | A/C | 0.32 | 0.24 | intron-variant | Asb9 | Mm_Celera | X:164510745 | CACCTTTTTCACATC[A/C]CAGATACTCCATTCT | 69299 |
rs31455095 | snp | A/G | 0.375 | 0.216506 | intron-variant | Asb9 | Mm_Celera | X:164501744 | ATCAAGGACCAGATA[A/G]CCATCAAGACTCTTC | 69299 |
rs31455098 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Asb9 | Mm_Celera | X:164501787 | CATAGAAAGCTGCTC[A/C]TTTGGCCTTGTGGGC | 69299 |
rs31455101 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Asb9 | Mm_Celera | X:164502102 | AAGAATACCCCATTA[C/T]GTTAACTTTTTAAAA | 69299 |
rs31455244 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Asb9 | Mm_Celera | X:164510891 | GAATGGAGCAATTAG[A/T]GCACTTTAAATCTCT | 69299 |
rs31455247 | snp | C/G | 0.32 | 0.24 | intron-variant | Asb9 | Mm_Celera | X:164511016 | TTTCCTTTTTAAAGG[C/G]CAAGTTTAATGACAC | 69299 |
rs31455250 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Asb9 | Mm_Celera | X:164511075 | TCATAAGAGGTCCAT[C/T]CCCTAGTTTACCCAT | 69299 |
rs31455253 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Asb9 | Mm_Celera | X:164511096 | GTTTACCCATAAGCT[A/G]CACTGATTGATCCAT | 69299 |
rs31455375 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Asb9 | Mm_Celera | X:164528129 | TGGGAATGCAATTGT[C/T]CCTTTGCTTTGGGGA | 69299 |
rs31455377 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Asb9 | Mm_Celera | X:164528959 | GGGATGTTACCGCCA[A/G]GAGACATGAGTCACT | 69299 |
rs31455380 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb9 | Mm_Celera | X:164529115 | AGCAGAATGCCAAGT[A/G]CTCCACAAACAAGAA | 69299 |
rs31455383 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Asb9 | Mm_Celera | X:164529253 | CCCTTCTTGCCTTTT[G/T]TGTTTTTACATTATA | 69299 |
rs31455744 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Asb9 | Mm_Celera | X:164515642 | ATGAACACATGTGCT[C/T]ACACAGAAGTACACA | 69299 |
rs31455747 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Asb9 | Mm_Celera | X:164515658 | ACACAGAAGTACACA[C/T]AGACTTGCAACATAT | 69299 |
rs31455750 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Asb9 | GRCm38.p3 | X:164520376 | TTAAATTAGTAGAAT[C/T]CTATGCAAAGACACC | 69299 |
rs31455753 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb9 | GRCm38.p3 | X:164520402 | ACACCATTTAAAAAG[C/T]AGTTTACATCCTAAC | 69299 |
rs31456044 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Asb9 | Mm_Celera | X:164502142 | TGTTTGACTCTTCCG[A/C]TACTCCTTGGCAGAC | 69299 |
rs31456047 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Asb9 | Mm_Celera | X:164502211 | CTCGGCTTGCAGCAC[C/T]TGCATCGCCCGCTGA | 69299 |
rs31456050 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Asb9 | Mm_Celera | X:164502557 | GGGTGACCCACCATA[C/T]TTCTTCATTGGAAGT | 69299 |
rs31456053 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb9 | Mm_Celera | X:164502689 | TCTTGTGAAAAATGC[C/T]CCTTGGAATGTGTGT | 69299 |
rs31456136 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Asb9 | Mm_Celera | X:164511282 | GTTGATGAAAAAGGG[A/G]TAGTGTGGCCTTGGA | 69299 |
rs31456139 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Asb9 | Mm_Celera | X:164511316 | CTCTGTCATGCCATG[A/G]ATAGTCTCCTACCAT | 69299 |
rs31456142 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Asb9 | Mm_Celera | X:164511526 | GGCATTTCTAGGTCT[C/T]TCCTCTATTGGCTGT | 69299 |
rs31456316 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb9 | Mm_Celera | X:164529935 | TGGGGTCTATTTTAA[A/G]CCACTCCAAAATCTG | 69299 |
rs31456319 | snp | G/T | 0.32 | 0.24 | intron-variant | Asb9 | Mm_Celera | X:164530093 | AGCTTGGGATGGCTG[G/T]CATGCTGGAGTAAGA | 69299 |
rs31456322 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Asb9 | Mm_Celera | X:164530584 | CAAAAGTCTGGAAGT[A/G]AAATTGGGCAAATTT | 69299 |
rs31456554 | snp | C/G | 0.32 | 0.24 | downstream-variant-500B | Asb9 | Mm_Celera | X:164539856 | AGAGTGTGAAGACTG[C/G]TTGTCCTCTGCTTAA | 69299 |
rs31456557 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B | Asb9 | Mm_Celera | X:164540172 | TGACATGGAACAGGA[A/G]ATGAAGGAGGACAGT | 69299 |
rs31456576 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb9 | Mm_Celera | X:164520525 | TGTGTGTCTGTCTCA[C/T]ACATGCTTGTATGTA | 69299 |
rs31456579 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb9 | Mm_Celera | X:164520562 | GGTGGAACCCAGGAC[C/T]TTCTATAGAACAATA | 69299 |
rs31456582 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb9 | Mm_Celera | X:164520797 | TTAATGATTACTATT[C/T]ACTGAAGATGTCTGT | 69299 |
rs31457026 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Asb9 | Mm_Celera | X:164503082 | GAAAAGATTCAAAGT[A/G]TTAGTGTAGCAAGCT | 69299 |
rs31457029 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb9 | Mm_Celera | X:164503292 | GTTGGAAGTACATTT[C/T]TTACTTTCCACCAAA | 69299 |
rs31457032 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Asb9 | Mm_Celera | X:164504582 | TCTCTAGAGAGACTT[C/T]CAAGTGCAGCCAAAG | 69299 |
rs31457105 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb9 | Mm_Celera | X:164511781 | CCTGAGATTTGCTGA[A/G]GCATTTTTTTTTGTA | 69299 |
rs31457108 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Asb9 | Mm_Celera | X:164511818 | TAACATAAGTTTAGG[A/C]TCAGGGCCTATGTTT | 69299 |
rs31457111 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb9 | Mm_Celera | X:164511849 | TTCTTCAAGGAAGGA[A/G]CATGGGCTTAACAAA | 69299 |
rs31457125 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb9 | Mm_Celera | X:164530900 | TGACAAGATAGAAGC[A/G]TCCATGTGGATTTGG | 69299 |
rs31457128 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb9 | Mm_Celera | X:164531546 | TCAGTTCACATCAGT[C/T]CCTCTCTTTACCCTG | 69299 |
rs31457131 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Asb9 | Mm_Celera | X:164531716 | GGCCTCTCCCATCCA[C/T]GAGGCTGCTAAAAGA | 69299 |
rs31457485 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb9 | Mm_Celera | X:164520966 | AAAATTTATACTACC[C/T]CAAGACACTGCTTTA | 69299 |
rs31457488 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb9 | Mm_Celera | X:164521004 | TTTGCAAGCAGCAGC[C/T]TATTATAGATTCTAT | 69299 |
rs31457491 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb9 | Mm_Celera | X:164521056 | AGTTAGTTTACTCAG[A/G]TTAAAAGAAGATTTG | 69299 |
rs31457854 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Asb9 | Mm_Celera | X:164512551 | CACTCTCTACTTCTA[A/C]AAGACACAAGGTGTC | 69299 |
rs31457857 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Asb9 | Mm_Celera | X:164512628 | AGACTTGCTTTTGAT[A/C]TTGGGAGGAACGTTA | 69299 |
rs31457860 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Asb9 | Mm_Celera | X:164512654 | CGTTATTCTGTATTT[G/T]CTGTAACAAAGAAAA | 69299 |
rs31457863 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Asb9 | Mm_Celera | X:164512818 | CCTGTCAAGTATTAT[A/G]ATCTGAGACAGCATT | 69299 |
rs31457905 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Asb9 | Mm_Celera | X:164504606 | GCCAAAGCAATATGC[A/G]CAGAGACACTGATTA | 69299 |
rs31457908 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb9 | Mm_Celera | X:164504837 | GCACCACCACTGTCC[A/G]GTGCAAAGAAATGCT | 69299 |
rs31457910 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb9 | Mm_Celera | X:164505314 | CAGCTCAGAGGCTTC[C/T]GAGGATAAAGCATTC | 69299 |
rs31457913 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Asb9 | Mm_Celera | X:164505533 | GGTAACAACACCAGC[G/T]ATTGACTGAAACCAA | 69299 |
rs31457984 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb9 | Mm_Celera | X:164531800 | TAACTACAGAAATAG[A/G]AAAGCAGAGGGATAT | 69299 |
rs31457987 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Asb9 | Mm_Celera | X:164531933 | TATGTTTGAGAATCA[C/T]CCTTTCAGAGCTATA | 69299 |
rs31457990 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Asb9 | Mm_Celera | X:164532078 | AACATTTTCTTTCAA[A/G]GTTATCATGTACCTC | 69299 |
rs31457993 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb9 | Mm_Celera | X:164533026 | ATTAGCCTTGTTTCT[C/T]CATGTCTCTTCCCTG | 69299 |
rs31458025 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb9 | Mm_Celera | X:164534500 | TTGTCAGCTTTCCTG[C/T]GGTAACAGAATCAAT | 69299 |
rs31458028 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb9 | Mm_Celera | X:164534603 | TCCCATAGCTTTAAA[C/T]GCAGTGCTGCCCAGT | 69299 |
rs31458030 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb9 | Mm_Celera | X:164534760 | TTGTACCATGCCCAT[A/G]CATAATACTCTGTGG | 69299 |
rs31458033 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Asb9 | Mm_Celera | X:164534774 | TGCATAATACTCTGT[A/G]GTGGTGAATTGCTAA | 69299 |
rs31458314 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Asb9 | Mm_Celera | X:164521071 | GTTAAAAGAAGATTT[A/G]CACTATTTGGATAGT | 69299 |
rs31458317 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Asb9 | Mm_Celera | X:164521347 | CCTCTCCAGCCCTAT[G/T]TATCTCTTGTTAACA | 69299 |
rs31458320 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Asb9 | Mm_Celera | X:164521462 | TAAGTGAGTTGTCAT[A/G]TTTGGACATCAATTC | 69299 |
rs31458323 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Asb9 | Mm_Celera | X:164521552 | GAGCAAATGCTCATC[C/G]CAATATTCAGTGGCA | 69299 |
rs31458515 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Asb9 | Mm_Celera | X:164512933 | AGAGAGCGATTGGCG[A/T]CCAGTTGTGCATGTA | 69299 |
rs31458518 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb9 | Mm_Celera | X:164513036 | TCCATTATCAGCACC[C/T]GAAGAGTGGTATTGC | 69299 |
rs31458523 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb9 | Mm_Celera | X:164513198 | ATGTACCAAGCCCAA[A/G]ATTTTTAGAGCCAGG | 69299 |
rs31458656 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Asb9 | Mm_Celera | X:164533053 | CCTGATCAGACTAGT[C/T]ATAAACACACGATCC | 69299 |