SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1253 | snp | A/G | 0.133435 | 0.221162 | intron-variant | TLE1 | GRCh38.p7 | 9:81664878 | GGCCTGAGAATATTC[A/G]TTTCTAACAAGTTCC | 7088 |
rs2591 | snp | C/T | 0.198324 | 0.244601 | intron-variant | TLE1 | GRCh38.p7 | 9:81673438 | TTTGCAAAAACAAAA[C/T]GGAAGTATCAGTGAA | 7088 |
rs8782 | snp | C/T | 0.380121 | 0.213468 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590945 | CCTGGCGGCTCCAAC[C/T]CCGCGCATCAAGGCG | 7088 |
rs10420 | snp | A/C | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81584003 | CCTGTCTACATAGAC[A/C]AAATGGAGCACCAAG | 7088 |
rs747151 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81655757 | GGATTTCTACTTTGT[C/G]TTTTTCCATTCTCTA | 7088 |
rs753484 | snp | A/G | 0.366885 | 0.220993 | intron-variant | TLE1 | GRCh38.p7 | 9:81673244 | CGCCATTGCACTCCA[A/G]CCTGGGGGACAAGAG | 7088 |
rs815843 | snp | A/G | 0.122411 | 0.214991 | intron-variant | TLE1 | GRCh38.p7 | 9:81626393 | GCAGGGTGATGGCTT[A/G]ATTGACACCAGGTGT | 7088 |
rs815844 | snp | C/T | 0.142609 | 0.225759 | intron-variant | TLE1 | GRCh38.p7 | 9:81601890 | CAGGAAACAAATGTT[C/T]GTTGCCTTGAATAGG | 7088 |
rs815845 | snp | G/T | 0.275999 | 0.248644 | intron-variant | TLE1 | GRCh38.p7 | 9:81601175 | TGTTTTTGTCTAGAT[G/T]CCACAGCTCGCTTAT | 7088 |
rs815846 | snp | C/T | 0.402806 | 0.197864 | intron-variant | TLE1 | GRCh38.p7 | 9:81607990 | GCTTTTTAGGAAAGC[C/T]GATTCCCATTGCTCT | 7088 |
rs815847 | snp | A/G | 0.5 | 0.00019968 | intron-variant | TLE1 | GRCh38.p7 | 9:81607703 | AGATAGGAAATGCTC[A/G]CAAGTGCCCCAAGGA | 7088 |
rs815848 | snp | A/G | 0.290201 | 0.246747 | intron-variant | TLE1 | GRCh38.p7 | 9:81607021 | GCCTAGGCTGGTTTC[A/G]AACTCCTGGGCTCAA | 7088 |
rs815849 | snp | A/C | 0.0829062 | 0.185956 | intron-variant | TLE1 | GRCh38.p7 | 9:81606802 | ACTGCCTCTCTCTCT[A/C]TATATATATATATGG | 7088 |
rs815850 | snp | G/T | 0.301932 | 0.244547 | intron-variant | TLE1 | GRCh38.p7 | 9:81606787 | ATATATATATATATG[G/T]ttttttttttaatta | 7088 |
rs815851 | snp | A/G | 0.395087 | 0.203592 | intron-variant | TLE1 | GRCh38.p7 | 9:81606417 | AGTATTCCATGGTGT[A/G]TATGTGCCACATTTT | 7088 |
rs815852 | snp | C/G | 0.249886 | 0.25 | intron-variant | TLE1 | GRCh38.p7 | 9:81606164 | acagtcccatcaaca[C/G]tgtaaaagtgttctt | 7088 |
rs815853 | snp | C/T | 0.256897 | 0.249905 | intron-variant | TLE1 | GRCh38.p7 | 9:81605785 | cgtgcagaaactctt[C/T]agtttaattagatcc | 7088 |
rs815854 | snp | A/T | 0.298651 | 0.24522 | intron-variant | TLE1 | GRCh38.p7 | 9:81604642 | GCCTCGTGCAGTGAC[A/T]GTGTGCCTCTGACCG | 7088 |
rs815855 | snp | A/C | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583878 | GATCACGCCTTGCCC[A/C]AGTGTGAGATTACCT | 7088 |
rs815857 | snp | C/T | 0.428937 | 0.17459 | intron-variant | TLE1 | GRCh38.p7 | 9:81595798 | AGACAGAGTCTCTGT[C/T]GCCCAGGCTGGAGTG | 7088 |
rs815858 | snp | A/G | 0.163892 | 0.234703 | intron-variant | TLE1 | GRCh38.p7 | 9:81595750 | ctcaccacaagctcc[A/G]cctcccaggttcacg | 7088 |
rs815859 | snp | A/G | 0.163236 | 0.234461 | intron-variant | TLE1 | GRCh38.p7 | 9:81595556 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 7088 |
rs815860 | snp | A/G | 0.278664 | 0.248351 | intron-variant | TLE1 | GRCh38.p7 | 9:81594634 | CACTTATTGTTTATG[A/G]TTTGAACTTCTAGCT | 7088 |
rs815861 | snp | A/T | 0.293551 | 0.246177 | intron-variant | TLE1 | GRCh38.p7 | 9:81593782 | GAAAGTTGAAGTCCA[A/T]ACCATAAACTGGTAT | 7088 |
rs843816 | snp | C/T | 0.183568 | 0.241012 | intron-variant | TLE1 | GRCh38.p7 | 9:81604701 | AGGGACCTTAATGTC[C/T]CTTTAGTATAAATGC | 7088 |
rs864179 | snp | A/G | 0.36955 | 0.219562 | intron-variant | TLE1 | GRCh38.p7 | 9:81596905 | ATACCATACACATAC[A/G]GAAAAGTGCATGAAT | 7088 |
rs870713 | snp | A/C | 0.415399 | 0.187465 | intron-variant | TLE1 | GRCh38.p7 | 9:81612243 | AATTAAGAGTATTCC[A/C]TACCCAATTTACAGA | 7088 |
rs873755 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TLE1 | GRCh38.p7 | 9:81612451 | CTGTTGCCTATTTTC[C/T]TTTGGGCCCAGGTTG | 7088 |
rs874754 | snp | C/T | 0.46014 | 0.13543 | intron-variant | TLE1 | GRCh38.p7 | 9:81635690 | TTTGCGTGCACTGAA[C/T]ATATTAAATCTTCAT | 7088 |
rs911638 | snp | A/G | 0.174932 | 0.238463 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589485 | ATAGAATGGGGTAGC[A/G]TCTTACAAATCTTTC | 7088 |
rs911639 | snp | C/T | 0.364609 | 0.222182 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589459 | CTTTCTCTGGACCAC[C/T]CACAGGTGGCTAGTG | 7088 |
rs944592 | snp | A/G | 0.439918 | 0.162576 | intron-variant | TLE1 | GRCh38.p7 | 9:81613140 | TTTTTTTCTTGAGAC[A/G]AAGTCTCGCTCTTGT | 7088 |
rs944593 | snp | C/G | 0.484421 | 0.0868729 | intron-variant | TLE1 | GRCh38.p7 | 9:81611625 | ACAAAGACGCCCAGT[C/G]TCCCAGCCACACACT | 7088 |
rs947672 | snp | A/T | 0.428786 | 0.174744 | intron-variant | TLE1 | GRCh38.p7 | 9:81640218 | AGAACATGAATTCTA[A/T]TTAATGGCACAGAAT | 7088 |
rs947673 | snp | A/C | 0.141258 | 0.225111 | intron-variant | TLE1 | GRCh38.p7 | 9:81640202 | TTAATGGCACAGAAT[A/C]TCAGCTTAGGTCTAA | 7088 |
rs1047377 | snp | A/C | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81633522 | AATTTTCAGGAAATC[A/C]CTGTATTAGGAATGT | 7088 |
rs1159642 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | TLE1 | GRCh38.p7 | 9:81658335 | TCCTCCTGTTTCAGG[A/C]TTATCCAGTCTAACC | 7088 |
rs1331865 | snp | A/G | 0.314301 | 0.241589 | intron-variant | TLE1 | GRCh38.p7 | 9:81624785 | TTTGTTTATTTGTTT[A/G]TTTTTTTAATTTTAA | 7088 |
rs1342477 | snp | C/T | 0.406296 | 0.19512 | intron-variant | TLE1 | GRCh38.p7 | 9:81632305 | TCCTTCAACCATTCC[C/T]CACTCCTCCACGCAC | 7088 |
rs1342478 | snp | A/G | 0.286825 | 0.247273 | intron-variant | TLE1 | GRCh38.p7 | 9:81632511 | TACCATATTAAACAC[A/G]GTCAAAATACTGCTA | 7088 |
rs1385041 | snp | A/C | 0.230603 | 0.249246 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690747 | GGTTTTTCAGGTCTC[A/C]GTGCTGGTTTATTAC | 7088 |
rs1385042 | snp | C/T | 0 | 0 | synonymous-codon, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687360 | GATTAAAGAGGAATT[C/T]CAGTTCCTGCAGGCG | 7088 |
rs1484112 | snp | C/T | 0.0562307 | 0.157967 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81691199 | GTCTGTTTAAATAAG[C/T]TCCTTCCCGTAAGTC | 7088 |
rs1484113 | snp | A/C | 0.316726 | 0.240931 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690817 | CCCATTTAGCTCTTC[A/C]CACAGCTCAGCTCAG | 7088 |
rs1539375 | snp | A/G | 0.435837 | 0.167226 | intron-variant | TLE1 | GRCh38.p7 | 9:81607079 | aaaaaaaaaaaaTGG[A/G]GAGAGAGAGAGATTT | 7088 |
rs1539377 | snp | A/T | 0.455144 | 0.142885 | intron-variant | TLE1 | GRCh38.p7 | 9:81597507 | CTATCCAAACGTCCA[A/T]CTCTACTCTTTGGGC | 7088 |
rs1573077 | snp | A/T | 0.392325 | 0.205532 | intron-variant | TLE1 | GRCh38.p7 | 9:81597748 | TTAATGGGTTTTTAT[A/T]TCATTCATGTTTTAC | 7088 |
rs1573078 | snp | G/T | 0.457737 | 0.139088 | intron-variant | TLE1 | GRCh38.p7 | 9:81597621 | TAGGTGGGGGCTGGG[G/T]CTCAGTTCTGAGGCT | 7088 |
rs1804529 | snp | C/T | 0 | 0 | missense | TLE1 | GRCh38.p7 | 9:81593251 | CCTTCCACGTTACTG[C/T]AGACGGTCAGATGCA | 7088 |
rs1804530 | snp | G/T | | | missense | TLE1 | GRCh38.p7 | 9:81616660 | GACAACTTAGTTGTG[G/T]ATGTGTCTAATGAGG | 7088 |
rs1804531 | snp | A/G/T | 1.65097e-05 | 0.00287308 | synonymous-codon, missense | TLE1 | GRCh38.p7 | 9:81593037 | GAGCCCTGTCTCCCA[A/G/T]CTCGACTGTCTGAAC | 7088 |
rs1872196 | snp | A/G | 0.195837 | 0.244062 | intron-variant | TLE1 | GRCh38.p7 | 9:81673222 | AGGTTGCAGTGAACC[A/G]AGATTGCGCCATTGC | 7088 |
rs1888812 | snp | C/T | 0.471863 | 0.115225 | | | GRCh38.p7 | 9:81621814 | ATTGCCTTCCGGTCC[C/T]CAGTTTTGATTTCCT | 7088 |
rs2004967 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | TLE1 | GRCh38.p7 | 9:81673642 | ATCCCACTCACCTGT[C/T]TTCTCTTTTTCAAGG | 7088 |
rs2018988 | snp | A/T | 0.197703 | 0.244469 | intron-variant | TLE1 | GRCh38.p7 | 9:81636855 | CCACCACACCTGGCT[A/T]ATTGTTGTATTTTTA | 7088 |
rs2129105 | snp | C/T | 0.317451 | 0.240729 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687574 | CCCCATAGTGAAGGG[C/T]AAACTCGAGTTTGGG | 7088 |
rs2129106 | snp | A/C | 0.27278 | 0.24896 | intron-variant | TLE1 | GRCh38.p7 | 9:81679510 | ACCTCACGGGGAAAA[A/C]AAATCAGAAAACCTC | 7088 |
rs2228172 | snp | A/G | 0.109578 | 0.206837 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585614 | CGGGGAGTGGCTGGC[A/G]GTGGGCATGGAGAGC | 7088 |
rs2228173 | snp | A/G | 0.166621 | 0.235686 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81652232 | GGTGACCATGGCAGA[A/G]TTGAATGCCATCATC | 7088 |
rs2229270 | snp | C/T | 4.96307e-05 | 0.00498125 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585629 | GGGGTACTGCCCCAC[C/T]GGGGAGTGGCTGGCA | 7088 |
rs2244337 | snp | G/T | 0.324855 | 0.23853 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685779 | ATATTAGCAAACGTG[G/T]TAGCAGAGTGTAAAA | 7088 |
rs2244732 | snp | C/T | 0.316726 | 0.240931 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688527 | AGCGCTGCCCCCGCG[C/T]ACAGTCCCCGAGCGC | 7088 |
rs2265659 | snp | A/G | 0.409721 | 0.192325 | intron-variant | TLE1 | GRCh38.p7 | 9:81657927 | GCGAGACTCTGTCTT[A/G]AAAAAAAAAAAAAAA | 7088 |
rs2277162 | snp | C/T | 0.363985 | 0.222503 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690785 | CACACCCCACCCCCA[C/T]AGTCTGGGTGGTACT | 7088 |
rs2279353 | snp | C/T | 0.161267 | 0.233723 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688111 | GGCGGACCTTCTCGC[C/T]CTCAGCGGTGTAAGG | 7088 |
rs2291300 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685783 | TATGATATTAGCAAA[C/T]GTGTTAGCAGAGTGT | 7088 |
rs2310105 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675872 | cgcccagctaatttt[A/C]gtattttcagcagag | 7088 |
rs2378591 | snp | G/T | 0.390277 | 0.206936 | intron-variant | TLE1 | GRCh38.p7 | 9:81638512 | TCCTTTGTTGAAGGT[G/T]ATAAGTACAAGATTG | 7088 |
rs2488274 | snp | C/G | 0.275197 | 0.248727 | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689743 | CGCTGCGCTGCCATA[C/G]GCTCCGGGGAGGAGC | 7088 |
rs2506124 | snp | A/G | 0.322007 | 0.239405 | intron-variant | TLE1 | GRCh38.p7 | 9:81685443 | TGGAAATATAAACTA[A/G]CCTCTTTATTGACAG | 7088 |
rs2506125 | snp | C/T | 0.481319 | 0.0948228 | intron-variant | TLE1 | GRCh38.p7 | 9:81678538 | gcgtgagccactgct[C/T]ccagccCCTAAATTT | 7088 |
rs2627002 | snp | G/T | 0.172997 | 0.237846 | intron-variant | TLE1 | GRCh38.p7 | 9:81660099 | TTGAGAAGGCTTTTA[G/T]GTAGAAAGCTGTTAA | 7088 |
rs2627003 | snp | G/T | 0.499816 | 0.0095829 | intron-variant | TLE1 | GRCh38.p7 | 9:81659007 | GAAGGAGAATTGCTT[G/T]AACCAGGGAGTCGGA | 7088 |
rs2627004 | snp | G/T | 0.180383 | 0.240111 | intron-variant | TLE1 | GRCh38.p7 | 9:81658524 | AAGCTGGCTTGTCAG[G/T]ATAGTTTAAGATTAG | 7088 |
rs2627005 | snp | A/G | 0.420733 | 0.18262 | intron-variant | TLE1 | GRCh38.p7 | 9:81652826 | ATCAACGGATTTAAT[A/G]TTAAAGTTTTAGGTA | 7088 |
rs2627007 | snp | C/G | 0.420255 | 0.183066 | intron-variant | TLE1 | GRCh38.p7 | 9:81651297 | GTTCGTCCCCTTCCA[C/G]ACTAAGCCAAAGAAG | 7088 |
rs2627008 | snp | A/C | 0.428937 | 0.17459 | intron-variant | TLE1 | GRCh38.p7 | 9:81649968 | TGGATTAGTATATGA[A/C]TTTATGTCCGAAGGC | 7088 |
rs2627009 | snp | C/T | 0.175897 | 0.238765 | intron-variant | TLE1 | GRCh38.p7 | 9:81649349 | CCTGTGGGTGCTCTT[C/T]GAGGAGACAGAGAGA | 7088 |
rs2627010 | snp | A/C | 0.428786 | 0.174744 | intron-variant | TLE1 | GRCh38.p7 | 9:81649347 | TGTGGGTGCTCTTCG[A/C]GGAGACAGAGAGAGG | 7088 |
rs2627016 | snp | A/G | 0.321769 | 0.239477 | intron-variant | TLE1 | GRCh38.p7 | 9:81684521 | GGAGTTACAAAAGCA[A/G]AATTCAACTCTGAAA | 7088 |
rs2627017 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671624 | cactccaacctgggc[A/G]acagagtgagactcc | 7088 |
rs2627018 | snp | A/G | 0.413416 | 0.189196 | intron-variant | TLE1 | GRCh38.p7 | 9:81662951 | ttcctgggcttaagc[A/G]attctcatgcctcag | 7088 |
rs2777772 | snp | G/T | 0.180383 | 0.240111 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589417 | GACATTCAATAGGCT[G/T]TACATGGCCCTATTA | 7088 |
rs2777773 | snp | C/T | 0.151334 | 0.229706 | intron-variant | TLE1 | GRCh38.p7 | 9:81592230 | gggcgtggtggtggg[C/T]gcccgtagtcccagc | 7088 |
rs2777774 | snp | A/C | 0.268995 | 0.249277 | intron-variant | TLE1 | GRCh38.p7 | 9:81593432 | TTGAAGCATTTACTG[A/C]TGGTGCAAATTTAAA | 7088 |
rs2777775 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | TLE1 | GRCh38.p7 | 9:81597425 | TGAGGCAACAAAAAA[C/T]ACAAAATTCTTAAGT | 7088 |
rs2777776 | snp | A/G | 0.45692 | 0.1403 | intron-variant | TLE1 | GRCh38.p7 | 9:81598031 | AAACAATAATGAAGA[A/G]CCACAGACCCCAGAG | 7088 |
rs2777777 | snp | C/T | 0.459801 | 0.135955 | intron-variant | TLE1 | GRCh38.p7 | 9:81598245 | AAACTCCCAGCCACA[C/T]AGGACAACAGGCCAG | 7088 |
rs2777778 | snp | C/G | 0.193028 | 0.243422 | intron-variant | TLE1 | GRCh38.p7 | 9:81598381 | CCCTCTGCCTGCCAC[C/G]AACTCCCCAGCCTTG | 7088 |
rs2777779 | snp | C/G | 0.192401 | 0.243274 | intron-variant | TLE1 | GRCh38.p7 | 9:81598384 | TCTGCCTGCCACGAA[C/G]TCCCCAGCCTTGATG | 7088 |
rs2777780 | snp | C/G | 0.462582 | 0.131564 | intron-variant | TLE1 | GRCh38.p7 | 9:81598880 | CTGTGGCAGAAGCAA[C/G]CAGAGGTCACATGGA | 7088 |
rs2777781 | snp | A/T | 0.420266 | 0.183056 | intron-variant | TLE1 | GRCh38.p7 | 9:81600119 | AGGAACAAGGCTCCT[A/T]AACAGGACAAAGATA | 7088 |
rs2796442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81671570 | gaatggcgtgaaccc[A/G]ggaggcggagcttgc | 7088 |
rs2796443 | snp | C/T | 0.455263 | 0.142713 | intron-variant | TLE1 | GRCh38.p7 | 9:81677392 | AACATGATGAAATCC[C/T]GTCTCTACTAAAAAT | 7088 |
rs2796444 | snp | A/G | 0.304438 | 0.244001 | intron-variant | TLE1 | GRCh38.p7 | 9:81680082 | TCAATTTGCACGCAC[A/G]AGGTGCTGGGTTCTG | 7088 |
rs2796446 | snp | C/T | 0.405429 | 0.195811 | intron-variant | TLE1 | GRCh38.p7 | 9:81664165 | AAAATGGTGGGATTA[C/T]AGGCATGAGCCACCA | 7088 |
rs2796447 | snp | A/G | 0.376288 | 0.215757 | intron-variant | TLE1 | GRCh38.p7 | 9:81653963 | TTTAACAGCTGAACA[A/G]TTTTACTTACTTCCT | 7088 |
rs2796448 | snp | A/C | 0.495855 | 0.045338 | intron-variant | TLE1 | GRCh38.p7 | 9:81655246 | GTGGGCGCCTGTAAT[A/C]CCAGCTACTCGGGAG | 7088 |
rs2796449 | snp | C/T | 0.175576 | 0.238665 | intron-variant | TLE1 | GRCh38.p7 | 9:81655485 | ACTCTACTTCTAGCC[C/T]AGGGAAGGGTCCACC | 7088 |
rs2796450 | snp | C/T | 0.179105 | 0.239737 | intron-variant | TLE1 | GRCh38.p7 | 9:81660180 | GACACATTTCTTTGC[C/T]GTACCTCCCCTACTA | 7088 |