SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3685533 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Tle3 | Mm_Celera | 9:61386262 | TAAATATTTAATGGT[G/T]TTGTAGTTATATATA | 21887 |
rs3722895 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tle3 | Mm_Celera | 9:61403826 | GAGTGACCTCCAAAG[C/T]CCCCCTTACAAAGAG | 21887 |
rs6189241 | snp | C/T | 0.5 | 0 | intron-variant | Tle3 | Mm_Celera | 9:61406701 | CTCAGGCTTGTCATC[C/T]CTAGGGATTCCCCTC | 21887 |
rs6202438 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Tle3 | Mm_Celera | 9:61406889 | TTGTGACACTGGCTT[C/G]TCTTCCGTTTGTGGG | 21887 |
rs6202922 | snp | C/T | 0.5 | 0 | intron-variant | Tle3 | Mm_Celera | 9:61406940 | CCGGGCTCAGGGTTG[C/T]TCATCTCTGCTTAGG | 21887 |
rs6202966 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Tle3 | Mm_Celera | 9:61406966 | TTAGGGCTTTATCTG[C/T]AGCTCAGCACCTTTT | 21887 |
rs6203003 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Tle3 | Mm_Celera | 9:61406989 | CACCTTTTCTCATTC[A/G]CTGCCCAACTTAAAA | 21887 |
rs6222933 | snp | C/T | 0.5 | 0 | intron-variant | Tle3 | Mm_Celera | 9:61408351 | GGCAGGCCCCAGTTG[C/T]AGGTGGGNTGNTTTG | 21887 |
rs6222951 | snp | A/G | 0.5 | 0 | intron-variant | Tle3 | Mm_Celera | 9:61408359 | CCAGTTGNAGGTGGG[A/G]TGNTTTGGGACAGAT | 21887 |
rs6222954 | snp | A/G | 0.5 | 0 | intron-variant | Tle3 | Mm_Celera | 9:61408362 | GTTGNAGGTGGGNTG[A/G]TTTGGGACAGATCCT | 21887 |
rs6222980 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Tle3 | Mm_Celera | 9:61408383 | GACAGATCCTCTGTA[A/G]TAAGGTCTCTTCTGC | 21887 |
rs6223606 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle3 | Mm_Celera | 9:61408515 | GTCTAGGGTGGCCCT[A/G]TCTTCCCTCTCCAGG | 21887 |
rs6224042 | snp | C/T | 0.5 | 0 | intron-variant | Tle3 | GRCm38.p3 | 9:61408532 | CTTCCCTCTCCAGGG[C/T]TGGGGGANTATGCTT | 21887 |
rs6224057 | snp | A/G | 0.5 | 0 | intron-variant | Tle3 | Mm_Celera | 9:61408540 | TCCAGGGNTGGGGGA[A/G]TATGCTTTCCTGGAG | 21887 |
rs6224147 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Tle3 | Mm_Celera | 9:61408595 | ACCTTGCTGGTTAGC[A/G]TTCTGGACTTGTATG | 21887 |
rs6224665 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Tle3 | Mm_Celera | 9:61408661 | GGGCTCAGGGTCTAG[A/G]TTGTTCAGAGCTAAT | 21887 |
rs6394473 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Tle3 | Mm_Celera | 9:61403353 | GTGAGAGGTGGCTTT[A/G]ATAAACCACAAAGGT | 21887 |
rs6395061 | snp | C/T | 0.5 | 0 | intron-variant | Tle3 | Mm_Celera | 9:61403486 | AAGTGAAGGTGCTTT[C/T]GGTGTAGGGATGGGG | 21887 |
rs29641666 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle3 | Mm_Celera | 9:61378756 | GAGGCGTGGTGCTGG[A/G]GGAAGCCAGCCGGGA | 21887 |
rs29691708 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Tle3 | Mm_Celera | 9:61409542 | CAGGTCTGCCTGGTG[A/G]TCTTTCTTGTCAGGT | 21887 |
rs29740427 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Tle3 | Mm_Celera | 9:61406265 | GATAAGATAACTGGA[G/T]CGAGGAAGGATTATT | 21887 |
rs29831124 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Tle3 | Mm_Celera | 9:61376331 | ATCCTTTGATGGATA[C/T]GTAAACTACCTCACA | 21887 |
rs29837933 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Tle3 | Mm_Celera | 9:61383427 | TTGAGCTCTTAACAG[C/T]GCTTGCCTCTGCCTG | 21887 |
rs29893392 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Tle3 | Mm_Celera | 9:61408570 | GAGAATTTCCCATAA[A/G]GCCCTGTGAACCTTG | 21887 |
rs29987568 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle3 | Mm_Celera | 9:61375765 | GCTCTGCTGGGTTAT[A/G]TTGGGCTTTTAGCAT | 21887 |
rs29993648 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Tle3 | Mm_Celera | 9:61414904 | GAGAGCCAGCATGGG[A/G]AGCCTGGTCCAGTAG | 21887 |
rs30033979 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Tle3 | Mm_Celera | 9:61377317 | AGAAGTCACCTTGGC[C/T]GACAGAGCAAAGCTA | 21887 |
rs30035679 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Tle3 | Mm_Celera | 9:61396645 | CTGAGTGAATGCGGC[C/T]GTCGCCCTGTCATTA | 21887 |
rs30077441 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle3 | Mm_Celera | 9:61410397 | ACTTGAAGGCAGGAG[A/G]TGATGCAGAGGCCAT | 21887 |
rs30080076 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle3 | Mm_Celera | 9:61381644 | GCTGACACCAGCACT[A/G]GAGCAGAGACAAGTG | 21887 |
rs30224101 | snp | C/T | 0.387812 | 0.208586 | synonymous-codon | Tle3 | Mm_Celera | 9:61414794 | GGTCCTGCACCACAC[C/T]AAGCCCGACAAATAC | 21887 |
rs30228473 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle3 | Mm_Celera | 9:61381643 | TGCTGACACCAGCAC[C/T]GGAGCAGAGACAAGT | 21887 |
rs30233497 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Tle3 | Mm_Celera | 9:61385172 | ACCCCCAAAATTTAA[C/T]GAGCTGCCTCAGCAA | 21887 |
rs30233825 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Tle3 | Mm_Celera | 9:61409894 | CACTCTCACGGATGC[C/T]TCCTCCCCACTCATC | 21887 |
rs30235150 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Tle3 | GRCm38.p3 | 9:61401342 | GCCAAGGGCATCAGC[G/T]TTGATTCCACCAGTC | 21887 |
rs30290225 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Tle3 | Mm_Celera | 9:61381945 | GAAAGATTGTACCAC[A/G]CTTGAGGGGAGCCAG | 21887 |
rs30334815 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle3 | Mm_Celera | 9:61375873 | CAGGAGCTGTGTGAC[A/G]CCCGGAGGTAGAGAG | 21887 |
rs30381318 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Tle3 | Mm_Celera | 9:61417180 | AGGGAGGAACCCCAT[C/T]CCACCATTGCTCGCC | 21887 |
rs30426862 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Tle3 | Mm_Celera | 9:61377582 | GTATCCAGGAAGCCC[G/T]CATGGCAAGACCTAG | 21887 |
rs30437033 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Tle3 | Mm_Celera | 9:61414104 | AGGTGTGTAACCCAA[A/G]CACTGTGTGCTTCCT | 21887 |
rs32813634 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61384428 | AGGGTTTGGATGACG[A/T]GTGTGGTTGAAAGGT | 21887 |
rs32813636 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61384508 | TATCATGATCATGAA[C/T]CACTCTGGGCTTTGG | 21887 |
rs32813638 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Tle3 | Mm_Celera | 9:61384789 | CTGGGAGATGTGGTT[A/T]CCTTCGTCTTGATCT | 21887 |
rs32813640 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Tle3 | Mm_Celera | 9:61384797 | TGTGGTTACCTTCGT[C/G]TTGATCTGTGGAGAG | 21887 |
rs32813642 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Tle3 | Mm_Celera | 9:61384850 | CTCATCTTTGGCTTC[A/C]GAGAGGTGGGAGGTT | 21887 |
rs32813884 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Tle3 | Mm_Celera | 9:61399958 | TAAAAATTCATTTTT[A/T]AAAAAGGGAAAGTGG | 21887 |
rs32813886 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61400005 | TCCCATCGGAGAGGA[A/G]TCCAATCTTAGCTGA | 21887 |
rs32813888 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61400111 | GTCACATCGCTAAGA[C/T]CTGTGGCCACCAAAA | 21887 |
rs32813890 | snp | A/C/G | 0.231111 | 0.249285 | intron-variant | Tle3 | GRCm38.p3 | 9:61400267 | GTAAGACTGCCAGAA[A/C/G]AGCCTTAACTTGGAG | 21887 |
rs32813892 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61400320 | TCTGCAGCTCCGTTC[A/G]TTGAGGGGAATGTGG | 21887 |
rs32813934 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61392072 | CTGTACTGGGCAGGT[A/T]CTCTGGGTTGCATCA | 21887 |
rs32813936 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61392089 | TCTGGGTTGCATCAT[C/T]TGGCCCCACAGGATA | 21887 |
rs32813938 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61392141 | GGCTCCCGTCAGGGC[C/T]TGTTCTCTCCATAAA | 21887 |
rs32813940 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61392690 | TGTAGGAAACCTTTG[G/T]GTTCCATTCTTAGAC | 21887 |
rs32813942 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61392743 | CACCATACTGCAGGG[G/T]TTAGAAGCAACCGTC | 21887 |
rs32814264 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61384877 | GGTTTCCTGTCTGTC[A/T]GAGCAGTCGGTTTGC | 21887 |
rs32814267 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61385317 | GAATTTTTCCTCCTC[A/T]CAGGAGTTGGCCAGT | 21887 |
rs32814268 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61385824 | CTCGTCAGTGCTGCG[G/T]AAAGGCCCAGTGGGA | 21887 |
rs32814269 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61385990 | AGTGCCTAGAAGGGT[C/T]ATGTCACCACTCAGA | 21887 |
rs32814271 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61386080 | CTGTTCCTCCCTCTC[A/T]TGGGAAGGGCACAGG | 21887 |
rs32814273 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61386166 | TAAGACAGAGATCTT[A/C]GGGGTCATGCGGAGA | 21887 |
rs32814535 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61409554 | GTGATCTTTCTTGTC[A/G]GGTTTAAGGATATGG | 21887 |
rs32814537 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61409669 | GCTAAGTGTGAGGAA[A/C]GAGCATCTAACAGGT | 21887 |
rs32814539 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61409697 | GGTTGTTACCTTAGA[C/T]CTGTGTTCACTGTCT | 21887 |
rs32814541 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61409832 | TTGGGTAGCTTCAGA[A/T]CGTAAGAGGGCTATG | 21887 |
rs32814543 | snp | C/G | 0.387812 | 0.208586 | intron-variant | Tle3 | Mm_Celera | 9:61409861 | TGGCCTCAGCTTTGT[C/G]TATCAGAAGGGTGAG | 21887 |
rs32814544 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61392771 | GTCAAAGTAGAGGAC[A/G]AGGGCCACATGCCAC | 21887 |
rs32814546 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61392883 | TAGTGGGCAGCGCAG[A/T]TCTCTCAGCACTGGA | 21887 |
rs32814548 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61392925 | CGGGTTTTCTGGACT[A/G]TGGAGAGGTCTTTGT | 21887 |
rs32814550 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61392986 | TGCGAGCCATTGACC[C/T]GAGTCCCCTGTGAAA | 21887 |
rs32814552 | snp | G/T | 0.231111 | 0.249285 | synonymous-codon | Tle3 | Mm_Celera | 9:61393214 | GCAGACAGAGATTGC[G/T]AAGAGACTGAACACA | 21887 |
rs32814564 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61400346 | TGTGGGCAGCTTTTT[A/C]ATCCTTGGCCAGATC | 21887 |
rs32814566 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61400577 | GAGCTTGGGCTGCCC[A/G]TTCCAGTGCCTCTCT | 21887 |
rs32814568 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61400659 | ACGGGTTTTATTTGG[A/T]TAGTATCCAGGAGTT | 21887 |
rs32814570 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61400675 | TAGTATCCAGGAGTT[C/T]ATATGCACATACAGG | 21887 |
rs32814572 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61400740 | GAAGAAAACTGTGTG[C/T]ACAAATGGGGACAAG | 21887 |
rs32814639 | snp | C/G | 0.124444 | 0.216185 | upstream-variant-2KB | Tle3, Gm34157 | Mm_Celera | 9:61370609 | AATTACTAGTCGAGA[C/G]TCTCTTTGCTGGTCT | 21887 |
rs32814641 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61382314 | TCGTGCAAATGTCAG[A/C]GACGAGAGTAACATG | 21887 |
rs32814643 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61382357 | TCCTGTAGCACTTGA[C/T]TGCCAAGCAGGTGAG | 21887 |
rs32815014 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61393475 | ACCTGAGGAGGGAGG[C/T]TGAGCCCTGTGACCA | 21887 |
rs32815016 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61393565 | TTCAAGTAAGGCTGG[C/T]TGGTTGGTGCCAAAG | 21887 |
rs32815018 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61393763 | TGTGCAGACCTCTGG[C/T]CCCCATTTCTATCCT | 21887 |
rs32815020 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61393787 | CTATCCTGTCTGATC[C/T]CACTCCAGCAGGGCC | 21887 |
rs32815022 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61393823 | CTACCCTACATTTAT[C/T]CCCTAAGGTGGCTCG | 21887 |
rs32815066 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Tle3 | Mm_Celera | 9:61409931 | CCTCATTCACATCCT[A/C]ACAGCCTCGGCCCTG | 21887 |
rs32815068 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tle3 | Mm_Celera | 9:61410221 | TATAGTACATATCCC[C/T]GCATGCTGAGGGGAT | 21887 |
rs32815070 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61410665 | TCTGTGGACACCTGA[C/T]AGCTGCTCTGGGAAG | 21887 |
rs32815071 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61410884 | GGTGGTGACAAACAG[A/G]ATTAAGGCTGGCAGA | 21887 |
rs32815073 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61410939 | TTTCTCTACTCTTCT[A/G]TACTTGGGGTGGCCC | 21887 |
rs32815144 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61400793 | CCCAAGAAATACTTC[C/T]ATCCCTGAGAAATAG | 21887 |
rs32815146 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61400840 | TGCCCTACAATGCCA[A/G]TGGTTGTTGGCAATC | 21887 |
rs32815148 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61400879 | AACAGGGCATTCTGT[C/T]TTGGCTGCTGGGGAA | 21887 |
rs32815150 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61400921 | TCTGAGCTAGGAACT[C/T]GGGCACGGGAGCAGA | 21887 |
rs32815152 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61400962 | GAGCCTTGACGTTAG[C/T]AATGGGAAGAGGTGC | 21887 |
rs32815275 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61382663 | CTGCTGACCAAGGTT[A/G]TGGTTGTAAAAGGGA | 21887 |
rs32815277 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61383147 | GTGAAAGAGAGAAGA[A/G]GGGCCAAGGTCACTA | 21887 |
rs32815279 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61383315 | TACCATTGTTTTTCC[C/T]AGCAGAGCCCCTTCT | 21887 |
rs32815281 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61383355 | TCTCAAGGAGGAGAC[C/G]GCAGCCCAATTTAGC | 21887 |
rs32815283 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle3 | Mm_Celera | 9:61383382 | TAGCTTTGCCTCAGA[A/G]TAGAAGTCCTGGGGG | 21887 |
rs32815395 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle3 | Mm_Celera | 9:61386221 | CTTCCTAGCAGAAAG[A/G]CTCCAGCAGGCTTTC | 21887 |