SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6171543 | snp | C/T | 0.5 | 0 | intron-variant | Map3k3 | Mm_Celera | 11:106135880 | agcatttctttagtc[C/T]tgcctgtcctggaac | 26406 |
rs6172146 | snp | A/G | 0.5 | 0 | intron-variant | Map3k3 | Mm_Celera | 11:106136020 | tttattgctctgtga[A/G]ttgagttcacggcag | 26406 |
rs6272882 | snp | A/G | 0.5 | 0 | intron-variant | Map3k3 | Mm_Celera | 11:106120470 | GAACATTGTGCTGGT[A/G]TTTATTCTTCATAAT | 26406 |
rs6273434 | snp | A/G | 0.5 | 0 | intron-variant | Map3k3 | Mm_Celera | 11:106120563 | GGTGGTTTACTATTG[A/G]NAAATTTAAACTGTT | 26406 |
rs6273437 | snp | C/T | 0.5 | 0 | intron-variant | Map3k3 | Mm_Celera | 11:106120564 | GTGGTTTACTATTGN[C/T]AAATTTAAACTGTTT | 26406 |
rs6335935 | snp | A/G | 0.5 | 0 | intron-variant | Map3k3 | Mm_Celera | 11:106136206 | TGGTTGAGACAGGAA[A/G]TACACAAAATTCTTT | 26406 |
rs6336516 | snp | C/T | 0.5 | 0 | intron-variant | Map3k3 | Mm_Celera | 11:106136335 | atacactctagggga[C/T]atagcttagacctca | 26406 |
rs13481209 | snp | A/G | 0.402042 | 0.198452 | intron-variant | Map3k3 | Mm_Celera | 11:106114327 | GAAGGACAGCTATGC[A/G]CATTTTCTTACATTT | 26406 |
rs27010932 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106152140 | GCCTTCCCACAGTTT[C/T]CAGGCACCTGGAAGG | 26406 |
rs27010933 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106151392 | GCACAGCCTTTCCCT[A/C]GAGCAGTGGAGTCCC | 26406 |
rs27010934 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106151380 | CATGTCAGGTAAGCA[C/G]AGCCTTTCCCTCGAG | 26406 |
rs27010935 | snp | A/G/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | GRCm38.p3 | 11:106151335 | AACGGCCCAGGTTCC[A/G/T]TCTAACTTGAGAGTC | 26406 |
rs27010936 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106150571 | TCAGTGTCCCAAAGC[A/G]ACTGGAGCCCATGGG | 26406 |
rs27010937 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106149753 | GTGCGCTGCTCTGGC[C/G]CATCCTTCCCACTCT | 26406 |
rs27010938 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Map3k3 | Mm_Celera | 11:106149453 | GCCAGGCTCTGACTT[G/T]CTCTGTCCTCACTCT | 26406 |
rs27010939 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106149316 | CTGAGGAGCAGTCTT[A/G]TGCCTTCCCTGTGTT | 26406 |
rs27010940 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106149183 | TGTATACTCCAGGGT[A/G]CCACCTTTTTGACGT | 26406 |
rs27010941 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106149139 | GTCCATGAAAATGCT[A/G]CCACTGCGAATGTTG | 26406 |
rs27010942 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106148957 | GTCAAAGACCAAACT[C/T]TGCCTGGAAAAAACA | 26406 |
rs27010943 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106148722 | ATTGGAAAGCCAAAA[C/T]GATAGAGTAATTTTC | 26406 |
rs27010944 | snp | A/C/G | 0.142012 | 0.225474 | intron-variant | Map3k3 | GRCm38.p3 | 11:106147998 | GTCCTAAGTTACAGA[A/C/G]GTATGAGGATTAAAT | 26406 |
rs27010945 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106146997 | TAGGGAGCAAAAAGG[C/T]ACAAGTACACATAGC | 26406 |
rs27010946 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106146103 | AAACAGGGATTCTCA[C/T]ACATAGGTTGGTCTG | 26406 |
rs27010947 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Map3k3 | Mm_Celera | 11:106145566 | TAACCCTTCCTCCAC[C/T]ACATGGGGAAACAAA | 26406 |
rs27010948 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106145482 | TTGGCAGAGCCCTAA[A/G]GAAGCCAGCCAAACA | 26406 |
rs27010949 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Map3k3 | Mm_Celera | 11:106145288 | TGTGAAATGAGGTGA[C/T]CTTATCTGTATAAAC | 26406 |
rs27010950 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Map3k3 | GRCm38.p3 | 11:106144700 | GCATATTTCTTCCCT[A/G]GGTTTTTTACTGACC | 26406 |
rs27010951 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Map3k3 | Mm_Celera | 11:106143634 | TAACCCATTTTGATG[A/G]CTAGTTGTTTGTTTG | 26406 |
rs27010952 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106143044 | GTTTTGCTATTTCTT[C/G]GTGAAGAGGGGGTTA | 26406 |
rs27010953 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Map3k3 | Mm_Celera | 11:106142920 | TACTATGAAGAGCCC[C/G]GAACTGACAGATGAT | 26406 |
rs27010954 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106142821 | TTAGGTGAGCACTTA[A/G]TGATAATTCACCTTT | 26406 |
rs27010955 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106142389 | CTGCGCCACATCTTG[G/T]CTCTGTTGTTAAAGG | 26406 |
rs27010956 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106142300 | CTTCCTCAAGCTGAA[A/C]ATGCTGAATTGCATG | 26406 |
rs27010957 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106142196 | CAGAGTTAGTTATGA[C/T]TCATGTTTTGTGTCA | 26406 |
rs27010958 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Map3k3 | Mm_Celera | 11:106139291 | TAGCGCAGCCAGAAA[A/G]TTTTATTATTATACA | 26406 |
rs27010959 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106136797 | GAAGCTGTCCTTTAA[A/T]CACTGAATGTGAGAC | 26406 |
rs27010960 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106136105 | ACCTAGATAAATTGT[C/G]TCCTGCAGGCTGCTG | 26406 |
rs27010961 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Map3k3 | Mm_Celera | 11:106134248 | CCAAGTAGAGGGTGA[A/G]TTCAGATGAAGGGAA | 26406 |
rs27010962 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106134168 | ACAGATATGTGAACT[G/T]CAGCAGGAGGTGCTT | 26406 |
rs27010963 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106133858 | TCTACCTGAGCTATA[C/T]CTTTCTTGCTTTTCC | 26406 |
rs27010964 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106133105 | GCAGCATGTGTACAG[C/T]TGGAGGAGTACAAAG | 26406 |
rs27010965 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106132914 | GAGGTAAAGGGACAT[G/T]GGAAGAGACCAAGAG | 26406 |
rs27010966 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106131989 | GCATTTTATGCTGAA[C/T]GCTCTTGTGTGATGT | 26406 |
rs27010967 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106131247 | AATATACCCCAGCAT[G/T]GTTCTTTGACTCCTA | 26406 |
rs27024768 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106129684 | AAAAAAAGTTTGCTT[A/G]TCATAATCTGGTCAG | 26406 |
rs27024769 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106129305 | CTGGAGGAGTCCCAT[A/T]GGCGTTGAAGAGAGA | 26406 |
rs27024770 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106129291 | CACCTAACAAGCTTC[C/T]GGAGGAGTCCCATAG | 26406 |
rs27024771 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106128979 | TTCACCGTGTGTGCT[C/T]GAGGTAAAAGACAAA | 26406 |
rs27024772 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106128900 | GTTGAGGCTAGCATC[C/G]CAGGCATGGGAAAGA | 26406 |
rs27024773 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106126330 | ATCATGGCACCATGA[A/G]TGACTTAGGTGGGAA | 26406 |
rs27024774 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106125830 | TTAAAAGTAAACTCT[A/C]AAACACGGGTATGAT | 26406 |
rs27024775 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106125214 | AGAGGCAAGATTGCA[A/G]TAGACCCTGTGCAGA | 26406 |
rs27024776 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106124915 | GCCACTAGGAAGCCA[A/G]GTTTTCCTTTTCACA | 26406 |
rs27024777 | snp | A/G | 0.18 | 0.24 | intron-variant | Map3k3 | Mm_Celera | 11:106124872 | TTGCATGTGCCTGCT[A/G]CCCTGATGATCTGAG | 26406 |
rs27024778 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Map3k3 | Mm_Celera | 11:106123881 | CTACCAAGCTCCTGA[A/G]CCCAGAAGCAGGCAC | 26406 |
rs27024779 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106123678 | AAACCTGGTAGCTAA[C/T]GCATTAAAAGGTGCC | 26406 |
rs27024780 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106123625 | TGAACATACAGCAAG[C/G]ATAGTGATGTGGCAA | 26406 |
rs27024781 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106123524 | GTGACGGATTACTAC[A/G]TGGATGTCTGTTACT | 26406 |
rs27024782 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106123328 | GGATTAATGATGAAT[A/G]CAGGAGGCCAGAGAG | 26406 |
rs27024783 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106123252 | CATCCTCAGTTTTCA[A/G]TTTTAAGCTTTCTCA | 26406 |
rs27024784 | snp | A/G | 0.32 | 0.24 | intron-variant | Map3k3 | Mm_Celera | 11:106121922 | TTCCAGAATTACTGT[A/G]CATTACTGGTTACCA | 26406 |
rs27024785 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106119975 | CACTCATGGTCTGAC[A/G]TAGGACAAGTGCTAC | 26406 |
rs27024786 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Map3k3 | Mm_Celera | 11:106119909 | GCGTAAGGTGACAGA[G/T]AGAGCTGTGGTACAG | 26406 |
rs27024787 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106119800 | TGAGAACTATCACCT[C/G]TGACTGACTGTGATG | 26406 |
rs27024788 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Map3k3 | Mm_Celera | 11:106118199 | CTGTGTGTGCATTGT[A/G]TGCTTGCAATCTTGA | 26406 |
rs27024789 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106118168 | TCCCTCTGGATGTAC[A/G]TTCTGTAATTGCATT | 26406 |
rs27024790 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106118063 | ACTTCTGTTCACTGG[A/G]GAAAAATGGCTGTAG | 26406 |
rs27024791 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106117473 | TTTGTATGATTTTCT[A/G]TGTCCTGTTGTTGTA | 26406 |
rs27024792 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106117328 | GGAATTACTTCACAT[A/T]GAGAGGAAACAAAAC | 26406 |
rs27024793 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106115201 | GAGCCACGTGCCTAA[C/T]CTCTTACTGTGTAGT | 26406 |
rs27024794 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106115155 | GTTGGGGACAATTGG[C/T]GTGAGTGAGCCATCC | 26406 |
rs27024795 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106115007 | CACCCAGGAAGAAGT[G/T]TTTTTGAAGATGACT | 26406 |
rs27024796 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106114522 | GGTGGGGTAAGATAT[A/G]GTACCAGAGCCAAGG | 26406 |
rs27024797 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106114463 | GAGATTATTTAGCTA[C/T]TTTCACCATCCTTAT | 26406 |
rs27024798 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Map3k3 | Mm_Celera | 11:106114322 | GCCAAGAAGGACAGC[C/T]ATGCGCATTTTCTTA | 26406 |
rs27024799 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Map3k3 | Mm_Celera | 11:106114214 | CCGGCCTGTGAGATA[C/T]GAAGATGTGGAGCAC | 26406 |
rs27024800 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106113490 | TCAATCCCAGCCTTT[A/G]TTGGTTTTCTTGACT | 26406 |
rs27024801 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106112785 | GGTTGCTTTCCCTTA[C/T]ACTGAGGCTCGAGAG | 26406 |
rs27024802 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Map3k3 | GRCm38.p3 | 11:106112705 | ATAACCAGACTTTGA[A/G]GCAGTTTAGGGTGAC | 26406 |
rs27024803 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106112648 | CAGTGCAGTGGCAGC[A/G]GCTTGGCTCTTATTA | 26406 |
rs27024804 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106111570 | TTGGAAGAGCTTCCT[A/G]GTGAAAGTACTGTGG | 26406 |
rs27024805 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106111432 | TGCCCCAGTACCTCT[A/G]CTCCTTTTCTTCTGA | 26406 |
rs27024806 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106111103 | CTTCCCTTTGTGTGT[C/T]TCCTTAGTTACTTGT | 26406 |
rs27024807 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106111076 | CTGCTGTTCCTTCCC[A/G]TACCTCCTCTCCTTC | 26406 |
rs27024808 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106110635 | ATTTGGAACAGGAGC[C/T]ATTAGGTGTTTTATT | 26406 |
rs27024809 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106108443 | TAATAGAACTAACAG[C/T]AGCAGCTATAGAAGC | 26406 |
rs27024810 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106107960 | CTGGGACTACATAAG[C/T]CTACACCACCACACC | 26406 |
rs27024811 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106107555 | TTTGAGAGCTGCAGT[A/G]GTTTTTAAGGTATGT | 26406 |
rs27024812 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106106528 | TAGTGTGGGAGTTGA[A/G]CATTAGTTGTCTTAA | 26406 |
rs27024813 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106106391 | TTGGGGGAAGGGTGA[A/G]AGAGGCCATGAAAGA | 26406 |
rs27024814 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Map3k3 | Mm_Celera | 11:106106314 | TGAGAACTCTCTGTT[A/T]AGAGGTTGACTAAAG | 26406 |
rs27024815 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Map3k3 | GRCm38.p3 | 11:106104691 | AACTCCTGGAAATAG[C/T]GTGAGGGTGTTCTTT | 26406 |
rs27024816 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | GRCm38.p3 | 11:106102588 | TGTCCAGCTTGAAAA[C/T]AAGATACATGTGAGC | 26406 |
rs27024817 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | GRCm38.p3 | 11:106102523 | TTCCTGTGGTACCCA[C/T]TGTAACTCCTCAGAA | 26406 |
rs27024818 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Map3k3 | Mm_Celera | 11:106101713 | CCAGGAGAGGTTATC[C/T]TTACCAGGCCAGAGA | 26406 |
rs27024819 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106100875 | GGCTTTGCTACACCG[C/T]ATCTCTTTAGCACTC | 26406 |
rs27024820 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106100849 | TTGGATGTACGACAC[A/G]TCCAGTGCATGGCTT | 26406 |
rs27024821 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106100809 | CCCTGGAAGCCAAGA[A/G]CATATTGAGATCTGG | 26406 |
rs27024822 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Map3k3 | Mm_Celera | 11:106100622 | AGGACTCTAGACATC[C/T]GCTTCCCTAAATAAA | 26406 |
rs27024823 | snp | A/C/T | 0.124444 | 0.216185 | intron-variant | Map3k3 | Mm_Celera | 11:106099810 | TCTGGGAAATGTAGA[A/C/T]GTTTCTGGAAAATAT | 26406 |