SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3726746 | snp | A/G | 0.5 | 0 | intron-variant | Tnip1 | GRCm38.p3 | 11:54912396 | AGCCCTGACTGTCCT[A/G]GAACTCACTCTGTAG | 57783 |
rs6250846 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tnip1 | GRCm38.p3 | 11:54914001 | CAGTTCTAACTGGCA[A/G]TAGATGTTGGCACTG | 57783 |
rs6307427 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Tnip1 | GRCm38.p3 | 11:54910905 | GGAGGCCGGAGTCAT[C/T]TCAGTCTGGGGCCCT | 57783 |
rs6308086 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Tnip1 | GRCm38.p3 | 11:54911074 | ACTCCTCACAGAGGG[A/G]CAAGGAGCAGGGGGC | 57783 |
rs6308561 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Tnip1 | GRCm38.p3 | 11:54911149 | GCACATGAGTTGGGT[A/G]TGGTCTCTGGAGAGC | 57783 |
rs13462994 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Tnip1, Gpx3 | Mm_Celera | 11:54910305 | TGAGAGGATAGCATG[C/T]CCTCCAGAGGCGCGG | 57783 |
rs26973808 | snp | C/T | 0.336735 | 0.234472 | upstream-variant-2KB | Tnip1 | Mm_Celera | 11:54964901 | CACCATTGCAGAGGG[C/T]GTTGTTGGATGGCAC | 57783 |
rs26973809 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB | Tnip1 | Mm_Celera | 11:54964017 | CTCTGTCTGCTTTCT[A/G]CAACTGTACCAGAAG | 57783 |
rs26973810 | snp | A/G | 0.486111 | 0.0821678 | upstream-variant-2KB | Tnip1 | GRCm38.p3 | 11:54963497 | AACCTGCCAGCTGCA[A/G]TCTGAGCATGCCACT | 57783 |
rs26973811 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB | Tnip1 | Mm_Celera | 11:54963476 | GGAAACCCTTGGCCC[A/G]TTCTGAACCTGCCAG | 57783 |
rs26973812 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Tnip1 | Mm_Celera | 11:54963474 | TTGGAAACCCTTGGC[C/T]CGTTCTGAACCTGCC | 57783 |
rs26973813 | snp | A/G | 0.197531 | 0.244432 | utr-variant-5-prime | Tnip1 | Mm_Celera | 11:54962897 | TGCCCAGTGAGTGCG[A/G]CCATGCCTCCCTGTG | 57783 |
rs26973814 | snp | A/G | 0.124444 | 0.216185 | utr-variant-5-prime | Tnip1 | Mm_Celera | 11:54962867 | TCCGAGAATGCACGA[A/G]GTGATCTGAAGATGT | 57783 |
rs26973815 | snp | C/G | 0.152778 | 0.230321 | utr-variant-5-prime | Tnip1 | Mm_Celera | 11:54962844 | CTACCTTCAGCCCAG[C/G]TCACTCATCCGAGAA | 57783 |
rs26973816 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tnip1 | Mm_Celera | 11:54962817 | ACGCTCCTGGAATCT[A/G]CCTTGTCACACCTAC | 57783 |
rs26973817 | snp | A/G | 0.32 | 0.24 | intron-variant | Tnip1 | Mm_Celera | 11:54962789 | GGTCTGGTGGCCTTG[A/G]CATTACCGTGTGACG | 57783 |
rs26973818 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Tnip1 | Mm_Celera | 11:54962607 | GAAGATTGGTCAGAA[C/G]AAGTACGAGGGAGAG | 57783 |
rs26973819 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tnip1 | Mm_Celera | 11:54962445 | TCCTGGGAGCCTGAC[A/G]CAAATGCAAACATGT | 57783 |
rs26973820 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tnip1 | Mm_Celera | 11:54961974 | CCTCATTCTGCAGTC[C/T]AGAGGTCACTGTCAA | 57783 |
rs26973821 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tnip1 | Mm_Celera | 11:54961485 | CTGGGGCTCACTTTG[C/T]CTGGATCTCACTGAG | 57783 |
rs26973822 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tnip1 | Mm_Celera | 11:54961457 | CCTCTCTCAGGGGAT[C/T]TCAGGCCTACTGCTG | 57783 |
rs26973823 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tnip1 | Mm_Celera | 11:54960488 | TTTGAGTGCTGGTGA[C/T]GATTACAGACGGTGC | 57783 |
rs26973824 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tnip1 | Mm_Celera | 11:54959312 | CAGGCTCTTATGCAT[C/T]GTATCACCACATCTC | 57783 |
rs26973825 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tnip1 | Mm_Celera | 11:54958427 | ATGTGGGTTACACGA[A/C]TCGCTAGACCTCACT | 57783 |
rs26973826 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Tnip1 | Mm_Celera | 11:54958400 | ACACAGTAGGCATCT[A/G]AAAAATGCCAGATGT | 57783 |
rs26973827 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tnip1 | Mm_Celera | 11:54958282 | TTTAACTTTACCTCC[A/G]CATCTTTCTCAGTTA | 57783 |
rs26973828 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tnip1 | Mm_Celera | 11:54958281 | CTTTAACTTTACCTC[C/T]GCATCTTTCTCAGTT | 57783 |
rs26973829 | snp | A/G | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Tnip1 | Mm_Celera | 11:54957170 | TGCAGGAGGAAGTGG[A/G]TCCTTGGTCCCTCCC | 57783 |
rs26973830 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Tnip1 | Mm_Celera | 11:54957077 | CACATTATGGAAAGA[C/T]GTGTGCATATACCTT | 57783 |
rs26973831 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Tnip1 | Mm_Celera | 11:54956324 | TGTTTTAGTTCCCAG[C/T]TGCAGGACCTGCTGT | 57783 |
rs26973832 | snp | A/G | 0.429688 | 0.173817 | intron-variant, upstream-variant-2KB | Tnip1 | Mm_Celera | 11:54956276 | ACCTCCCAGCGGGAC[A/G]GCACTAAGCGTCCGC | 57783 |
rs26973833 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Tnip1 | Mm_Celera | 11:54956201 | GTAAACAGCCGCAGT[A/G]GCTCCTCTGGGTGGA | 57783 |
rs26973834 | snp | C/G | 0.456747 | 0.140554 | intron-variant | Tnip1 | Mm_Celera | 11:54954437 | ACAGAAACATAGAAC[C/G]GTCCCACGGTGCACG | 57783 |
rs26973835 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tnip1 | GRCm38.p3 | 11:54954228 | TGAGGCATCGGGAAT[C/T]CACACGGTTCCCACA | 57783 |
rs26973836 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tnip1 | Mm_Celera | 11:54954019 | CTAGATACAAAGGAA[C/T]GCTGAGCCTGCTTAG | 57783 |
rs26973837 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Tnip1 | Mm_Celera | 11:54953519 | GAGGGTCCAGCTAAA[A/C]TATGAGACACTATCA | 57783 |
rs26973838 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Tnip1 | Mm_Celera | 11:54953491 | TGAATACATGTAAAA[C/T]TGAAATCGGACAGAG | 57783 |
rs26973839 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tnip1 | Mm_Celera | 11:54953098 | AAGCCAGCAGCAGAA[A/C]ATAGCCCTTGGGACT | 57783 |
rs26973840 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Tnip1 | Mm_Celera | 11:54952945 | CCCACAGGTCACCCA[C/T]GTGGAGGGGACAACA | 57783 |
rs26973841 | snp | A/G | 0.5 | 0 | intron-variant | Tnip1 | GRCm38.p3 | 11:54952916 | CTACGGGCATCCAGG[A/G]ACAGGCACCCACACC | 57783 |
rs26973842 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Tnip1 | Mm_Celera | 11:54952837 | GACATCCGGGCCAGA[G/T]ACACAGTACTGGGGG | 57783 |
rs26973843 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Tnip1 | Mm_Celera | 11:54952707 | AAAAAGCAGGTAGCA[A/G]GGCCTGCCAAATCAC | 57783 |
rs26973844 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Tnip1 | Mm_Celera | 11:54952659 | GGCATAAGGGCTCAG[C/T]GTGAGAACAGGCTGA | 57783 |
rs26973845 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Tnip1 | GRCm38.p3 | 11:54952275 | AAACAAGCTCTGGCA[C/T]ACAGATACAGCCTGA | 57783 |
rs26973846 | snp | A/C/G | 0.32 | 0.24 | intron-variant | Tnip1 | GRCm38.p3 | 11:54952223 | CTCCTGATGCTGTCA[A/C/G]AAAGAGCTCCCAGCC | 57783 |
rs26973847 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Tnip1 | Mm_Celera | 11:54952216 | CCCCTGGCTCCTGAT[A/G]CTGTCACAAAGAGCT | 57783 |
rs26973848 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Tnip1 | Mm_Celera | 11:54952158 | CAATCAGGTGCTCCT[G/T]AAAGACTTTATACCC | 57783 |
rs26973849 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Tnip1 | Mm_Celera | 11:54951895 | AGTAGGAGACAGTTC[C/T]AGCCTCACAGTTAGC | 57783 |
rs26973850 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Tnip1 | GRCm38.p3 | 11:54951880 | TGTCAGTCACAGGGG[A/T]GTAGGAGACAGTTCT | 57783 |
rs26973851 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Tnip1 | GRCm38.p3 | 11:54951746 | CGCCTGGGGCTAAGA[C/T]TCTAACAGCCTCAGC | 57783 |
rs26973852 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tnip1 | Mm_Celera | 11:54951677 | GCACAGAACGCAGGC[C/T]AGGAAAGGGTTTGAG | 57783 |
rs26973853 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Tnip1 | Mm_Celera | 11:54951304 | AAGCCAGAGATATCA[A/C]CAGAGGGCACAGAAA | 57783 |
rs26973854 | snp | C/G | 0.426035 | 0.177515 | intron-variant | Tnip1 | Mm_Celera | 11:54951260 | ATGACACCTCTCCTG[C/G]GTTCAAGATAGACAG | 57783 |
rs26973855 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Tnip1 | Mm_Celera | 11:54951149 | ACCCTTTCCAGTCTC[C/T]GGTGTGATCGTCCTG | 57783 |
rs26973856 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Tnip1 | Mm_Celera | 11:54951137 | TCCTCAGCAGTCACC[C/T]TTTCCAGTCTCTGGT | 57783 |
rs26973857 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Tnip1 | Mm_Celera | 11:54951114 | GCCATCAGAAAGGAC[A/G]CAGACAGTCCTCAGC | 57783 |
rs26973858 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Tnip1 | Mm_Celera | 11:54951100 | GCCCTTCAGGGACAG[A/C]CATCAGAAAGGACGC | 57783 |
rs26973859 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Tnip1 | Mm_Celera | 11:54951072 | GACAAGGTTAGTGAG[C/G]GAAGGATAGCCAGCC | 57783 |
rs26973860 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Tnip1 | Mm_Celera | 11:54950933 | GAATCATCTCAGGGT[C/T]CAGTGACTGGGCCCC | 57783 |
rs26973861 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Tnip1 | Mm_Celera | 11:54950688 | AGTTCCAGCATGAAT[G/T]CAAGGCCAGCCTGGG | 57783 |
rs26973862 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Tnip1 | Mm_Celera | 11:54950336 | CAGGGGAAGATGCCA[A/G]GTTTTGAGAACTCTC | 57783 |
rs26973863 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Tnip1 | GRCm38.p3 | 11:54949825 | TTAAATCACAGTATC[A/C]CTTCACAGTCCCAAT | 57783 |
rs26973864 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tnip1 | Mm_Celera | 11:54949762 | AGAAAGCCAAGTCCA[A/G]AGGGCAAGGCCTAAC | 57783 |
rs26973865 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Tnip1 | GRCm38.p3 | 11:54949078 | TTCCTTAACTCTGTA[A/G]GGCAGATCTAGACTC | 57783 |
rs26973866 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Tnip1 | Mm_Celera | 11:54948772 | AGTGGGACTGGTGTA[C/T]GCTTCATAAGAGCAA | 57783 |
rs26973867 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Tnip1 | Mm_Celera | 11:54948515 | CAGTGCCAAGACTGC[A/G]CAACAATGCAGACCT | 57783 |
rs26973868 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Tnip1 | Mm_Celera | 11:54948361 | TCTCCCAAAGCCCCA[A/C]ATGTCACAAAGCTTG | 57783 |
rs26973869 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Tnip1 | Mm_Celera | 11:54948309 | CAGTTGGGTCTCCTA[A/T]AGAAAAAAAGTAGCT | 57783 |
rs26973870 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Tnip1 | Mm_Celera | 11:54948270 | TTTGTTGACAGAGCC[C/T]TGGCATTCACATGTG | 57783 |
rs26973871 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tnip1 | Mm_Celera | 11:54948146 | CTATCACCTGCCAAT[C/T]GACTACCCTAGCTGC | 57783 |
rs26973872 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Tnip1 | Mm_Celera | 11:54948120 | GACCAGGTCTTGTTC[C/T]TGGCATTGCCCTATC | 57783 |
rs26973873 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Tnip1 | Mm_Celera | 11:54948119 | TGACCAGGTCTTGTT[C/G]CTGGCATTGCCCTAT | 57783 |
rs26973874 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tnip1 | Mm_Celera | 11:54948046 | AGGAACAAGATGTCA[C/T]GTTTCTCATGCTAGC | 57783 |
rs26973875 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tnip1 | Mm_Celera | 11:54947878 | CCAAAATGCAGTTTC[A/G]GAAGTTCTAAGGGGA | 57783 |
rs26973876 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tnip1 | Mm_Celera | 11:54947723 | TATCACCGTTACATC[C/T]GAAAATATAATCACT | 57783 |
rs26973877 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Tnip1 | Mm_Celera | 11:54947645 | GTCTCCATCTGAGGT[C/G]GGATCTTGTCTAGTG | 57783 |
rs26973878 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Tnip1 | Mm_Celera | 11:54947619 | ACAGAGAATGCCCCT[A/T]CACTGGTAATGTCTC | 57783 |
rs26973879 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Tnip1 | Mm_Celera | 11:54947136 | TCCCTGCTTTCCAAC[A/C]AGGAGGCCAATCCAC | 57783 |
rs26973880 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Tnip1 | Mm_Celera | 11:54946716 | AACAGAGCTGTCATC[A/G]GTCCCCAGGTCATCC | 57783 |
rs26973881 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Tnip1 | Mm_Celera | 11:54946683 | ATTCCTACTGCCGCA[A/G]CCCACCTTTCTGGCC | 57783 |
rs26973882 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tnip1 | Mm_Celera | 11:54945204 | CACTGGCACGGTCTT[A/G]TATATTACAATGCAC | 57783 |
rs26973883 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Tnip1 | Mm_Celera | 11:54945087 | AAGGACGGGAGTGAC[A/C]CAAGCCTCATGACTT | 57783 |
rs26973884 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Tnip1 | Mm_Celera | 11:54945082 | GGCCAAAGGACGGGA[C/G]TGACCCAAGCCTCAT | 57783 |
rs26973885 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tnip1 | Mm_Celera | 11:54944793 | GGTTTCTGGCTGTAT[C/T]AGGGGAGAGGCCTGG | 57783 |
rs26973886 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Tnip1 | GRCm38.p3 | 11:54944703 | TGACTGTCCCAAAAG[C/T]CCTGGGAAGAAGGCA | 57783 |
rs26973887 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Tnip1 | GRCm38.p3 | 11:54944592 | TGGGATCAGGCACCA[A/T]GAACAACGGGGGAGT | 57783 |
rs26973888 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Tnip1 | Mm_Celera | 11:54944563 | CTGCATTGCCATAGT[A/C]GTGGCTGAGAAGGTG | 57783 |
rs26973889 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Tnip1 | Mm_Celera | 11:54944350 | ACGACCTACACTCAC[A/T]GATCAACCAACAATA | 57783 |
rs26973890 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Tnip1 | GRCm38.p3 | 11:54944104 | AACTCTCCATTCACC[A/C]GAGCACAGTAGGAGG | 57783 |
rs26973891 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Tnip1 | Mm_Celera | 11:54943720 | GGTCCCTGCTTCGCT[A/G]AAGTTTCTACCTACT | 57783 |
rs26973892 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Tnip1 | GRCm38.p3 | 11:54943369 | AGCCAGAGGAACTTA[A/C]CCTACCTCCCAAGAG | 57783 |
rs26973893 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Tnip1 | Mm_Celera | 11:54943349 | ACATCCATTTCAAGG[C/T]CCAGAGCCAGAGGAA | 57783 |
rs26973894 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Tnip1 | Mm_Celera | 11:54943321 | AAAGCAGTTAAGTGT[A/G]GAGGTTCAATACACA | 57783 |
rs26973895 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Tnip1 | Mm_Celera | 11:54943140 | GCTGGATACATCCTG[A/G]GTGGCAAGTAGCTGC | 57783 |
rs26973896 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Tnip1 | Mm_Celera | 11:54943014 | CCACGTGACTGCACC[C/G]GGCTGGAGCCAGCAT | 57783 |
rs26973897 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Tnip1 | GRCm38.p3 | 11:54942565 | GTGTTAAGAACCTTC[A/T]ATGCTGGAGATGGAA | 57783 |
rs26973898 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tnip1 | Mm_Celera | 11:54942041 | CATGATGGCAATCCA[C/T]AGCTCCCACAATACA | 57783 |
rs26973899 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Tnip1 | GRCm38.p3 | 11:54941916 | CTCTGATGCATTCTG[C/T]TGGGTGCCCAGCAAC | 57783 |
rs26973900 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Tnip1 | Mm_Celera | 11:54941813 | GAACCTCAATGGCCA[A/T]GTTGACCTCCACACT | 57783 |
rs26973901 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tnip1 | Mm_Celera | 11:54941800 | CTGCTTCAGACAGGA[A/G]CCTCAATGGCCATGT | 57783 |