SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3024157 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tle4 | GRCm38.p3 | 19:14456802 | GCTCCAGGTCCTCCT[C/T]ATTTGACTCAGAGAA | 21888 |
rs3024158 | snp | G/T | | | intron-variant | Tle4 | GRCm38.p3 | 19:14456764 | TATTCACTTCCCAGC[G/T]TCTCCACCCTTTCCT | 21888 |
rs3024159 | snp | G/T | | | intron-variant | Tle4 | GRCm38.p3 | 19:14456713 | CAGTGCTGGGCTGCT[G/T]TTTGTAAACATGACC | 21888 |
rs3024160 | snp | A/G | | | intron-variant | Tle4 | GRCm38.p3 | 19:14456705 | GGCTGCTTTTTGTAA[A/G]CATGACCAGCTTAGA | 21888 |
rs4232065 | snp | G/T | 0.21875 | 0.248039 | utr-variant-3-prime | Tle4 | Mm_Celera | 19:14449501 | AGATTCCATTCACTG[G/T]TAGGTATTCCATGTT | 21888 |
rs4232066 | snp | A/T | 0.244898 | 0.249948 | utr-variant-3-prime | Tle4 | Mm_Celera | 19:14449525 | CCATGTTCTTCCAAG[A/T]CGATAGCTGAAGATT | 21888 |
rs4232067 | snp | A/G | 0.21875 | 0.248039 | utr-variant-3-prime | Tle4 | Mm_Celera | 19:14449603 | GAAGTGGGGCTATGG[A/G]AAGGGATTAAACTCC | 21888 |
rs4232068 | snp | A/T | 0.21875 | 0.248039 | utr-variant-3-prime | Tle4 | Mm_Celera | 19:14449631 | TCCACAACTGCAATG[A/T]GTATTGGAAATCCTT | 21888 |
rs6209538 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Tle4 | Mm_Celera | 19:14552231 | GATGAAAACACATGG[C/T]CAGGTGAAGCAAGAC | 21888 |
rs6210077 | snp | A/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14552353 | CCTGCATATACCTAA[A/T]TGTNAAATTCACAAA | 21888 |
rs6210091 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Tle4 | Mm_Celera | 19:14552357 | CATATACCTAANTGT[A/T]AAATTCACAAATTGG | 21888 |
rs6210643 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Tle4 | Mm_Celera | 19:14552457 | ACTGGAACCCATTTC[C/G]GAAACTGACAAACTG | 21888 |
rs6211156 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Tle4 | Mm_Celera | 19:14552542 | CTCCTAGTTTGAGCA[A/G]TTCAGCCAAGCCCAC | 21888 |
rs6211167 | snp | A/G | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14586072 | GACACTGAGGGTGGC[A/G]GGAAGGGGAACAGTT | 21888 |
rs6211261 | snp | C/G | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14552610 | TAAAACGTAAAGAAG[C/G]AATATGAGCAATTAG | 21888 |
rs6211696 | snp | A/T | 0.304688 | 0.243945 | intron-variant | Tle4 | Mm_Celera | 19:14552651 | TTACAGACCAATAAC[A/T]CTGCTACCAGTGCAT | 21888 |
rs6296654 | snp | C/G | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14596926 | GCCCGCGGTCCGAGA[C/G]GTGGGGGGGTTGGTC | 21888 |
rs6306622 | snp | G/T | 0.304688 | 0.243945 | intron-variant | Tle4 | Mm_Celera | 19:14552088 | TACAAGGCTGTCAAT[G/T]CGGCCTTTGGAGGGA | 21888 |
rs6307035 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Tle4 | Mm_Celera | 19:14552128 | TTAATTAAACCTGCA[A/G]GAGAAACAGAAAATG | 21888 |
rs6307076 | snp | C/T | 0.49926 | 0.0192165 | intron-variant | Tle4 | Mm_Celera | 19:14552147 | AAACAGAAAATGACC[C/T]CCTGAGAGTTATCTT | 21888 |
rs6307159 | snp | G/T | 0.304688 | 0.243945 | intron-variant | Tle4 | Mm_Celera | 19:14552191 | TCAAACAGATCATAC[G/T]GCTACCATTATGCCA | 21888 |
rs6332026 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Tle4 | Mm_Celera | 19:14598820 | AGAGGGAGGATCGCG[C/T]TGATCCCACTCCGTG | 21888 |
rs6333703 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Tle4 | Mm_Celera | 19:14599169 | AAGGAACCTCTGACC[C/T]CTGGGCAATCAAAAG | 21888 |
rs6341573 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Tle4 | Mm_Celera | 19:14481926 | GACAAACCAGTAAGG[A/G]ATAAGCATTCTGAGT | 21888 |
rs6341596 | snp | G/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14481942 | ATAAGCATTCTGAGT[G/T]CTCCGTACTGGCTCT | 21888 |
rs6341625 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Tle4 | Mm_Celera | 19:14481958 | CTCCGTACTGGCTCT[G/T]AGCCATTGGAGCACA | 21888 |
rs6341678 | snp | A/G | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14481993 | AAGAGACTACGAGGG[A/G]ACAggagggagggag | 21888 |
rs6342134 | snp | C/G | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14482045 | aggcagggaAATGGG[C/G]TGTGTTGTGGTGGGG | 21888 |
rs6342178 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Tle4 | Mm_Celera | 19:14482075 | GATGACACCCTGGCC[C/G]TATCCCAGAGCAATT | 21888 |
rs6371376 | snp | G/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14561230 | GAAACAGCCAAAAAG[G/T]GGGGGAGGGGGGCAC | 21888 |
rs6371918 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Tle4 | Mm_Celera | 19:14561347 | ATAGTTACTCTGTTA[C/T]TTACTTTTGGCAGCA | 21888 |
rs6372493 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Tle4 | Mm_Celera | 19:14561487 | AATTTTAAAACTGTA[C/T]ATCAACCTTAAGTAT | 21888 |
rs30304570 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14589532 | AACAAAAAAACACAC[A/G]AACAAACATGAGCCC | 21888 |
rs30307764 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14498945 | CATGTTCCCCCCCCC[A/C]CCCACACACACACAT | 21888 |
rs30312892 | snp | A/C | 0.42 | 0.183303 | intron-variant | Tle4 | GRCm38.p3 | 19:14481680 | TTTTTTTTAGACAAT[A/C]GAAAAATGATGGTAA | 21888 |
rs30315772 | snp | G/T | 0.375 | 0.216506 | intron-variant | Tle4, Gm31441 | GRCm38.p3 | 19:14566074 | ATGGAGAGGTGGGGA[G/T]AGAAATAAAAGATAA | 21888 |
rs30319902 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Tle4 | Mm_Celera | 19:14584747 | CTTTCTGTGCGGAGT[A/C]TAGTTCAGGAACAGA | 21888 |
rs30321729 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14457793 | AACATCCCCCACACT[A/G]ATACTAGCACTATTG | 21888 |
rs30322732 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Tle4 | GRCm38.p3 | 19:14554755 | CTCTAAGCTGTAACT[A/G]ATTTGTACCAGAAAG | 21888 |
rs30322734 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | GRCm38.p3 | 19:14465782 | TCAGGATACACCCAC[A/G]CAGGAATCACCATAG | 21888 |
rs30323350 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Tle4 | GRCm38.p3 | 19:14549123 | CAGTTCCAGTGGATC[C/T]AATACCCTTTTCTGA | 21888 |
rs30324508 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14543954 | ATTTTAATGAAAGTA[A/G]ATGGAATAATTAGCA | 21888 |
rs30325400 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14482558 | AGAATTTAAGCAAAC[A/T]GTGGTAAAAGCCAAG | 21888 |
rs30349940 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14583508 | GAATACTGGCTGCTC[C/T]TCCTGAGGACCCAGA | 21888 |
rs30354443 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14545183 | ACTCATCCCCTGTTC[A/C]TTTCTGCAGCTCCCT | 21888 |
rs30354691 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14581483 | CTACTTAGAAAACTC[G/T]GGATTTTATTGTATT | 21888 |
rs30355293 | snp | A/C | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14502174 | ACATATATATATTCC[A/C]CCCCCCCCCCCCATT | 21888 |
rs30355853 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Tle4 | Mm_Celera | 19:14455891 | TACATTGATCAGACT[C/T]GAAAATCACAAATTC | 21888 |
rs30357574 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14581419 | GCTCCCTCCTTGCAG[A/G]TAACTCTATTTTGTG | 21888 |
rs30357760 | snp | G/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14596648 | TCTGCCCACAGGGGG[G/T]AAATGGTAATACCTT | 21888 |
rs30359646 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14500007 | TCCTTCCACTGCTTC[C/T]TCATTTACATCCTGA | 21888 |
rs30363015 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14555652 | AGTGGACAGCCCATG[C/G]TAAAAAATATATTTG | 21888 |
rs30364756 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14576343 | CCCCCCAGATTATCA[C/T]CAATCAGCAGGACAG | 21888 |
rs30367184 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14574837 | CACTGAACGACAAGC[A/G]AGCTTGTGGGAGAGC | 21888 |
rs30371814 | snp | C/T | 0.487535 | 0.077957 | intron-variant, upstream-variant-2KB | Tle4 | GRCm38.p3 | 19:14550107 | AAAACCAAATGCTGT[C/T]TGGGTTGGTATGGGA | 21888 |
rs30372504 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14453477 | AGACGGAGACAAACA[A/C]ACAAACATACGACAC | 21888 |
rs30372619 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14581481 | AGCTACTTAGAAAAC[C/T]CGGGATTTTATTGTA | 21888 |
rs30372695 | snp | G/T | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14458505 | ACACTCAAAGAGTCT[G/T]CCAGAATAGCCTTGA | 21888 |
rs30376763 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Tle4 | Mm_Celera | 19:14576218 | TTTAAGATGACAATT[A/T]AAAAAATCACTTTAT | 21888 |
rs30400476 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Tle4 | GRCm38.p3 | 19:14543289 | CACTGTGTACATTAT[A/G]CTCCATGAAGTGGCA | 21888 |
rs30402227 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | GRCm38.p3 | 19:14524255 | TAAAGGGAACTGCAA[C/T]CCTATAGGTGGAACA | 21888 |
rs30402881 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14572409 | ACAGAATGTAGATGC[A/G]ACATAAATACCTTTA | 21888 |
rs30406075 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tle4 | GRCm38.p3 | 19:14578564 | CAAATTTAACTCAAG[C/T]TTCATGTTTACTATG | 21888 |
rs30408567 | snp | A/T | 0.32 | 0.24 | intron-variant | Tle4 | GRCm38.p3 | 19:14524248 | AAGTAGCTAAAGGGA[A/T]CTGCAACCCTATAGG | 21888 |
rs30409949 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | GRCm38.p3 | 19:14557949 | AGCTACTGTCCAAAC[A/G]CCTTTAATCCCAGCA | 21888 |
rs30410733 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Tle4 | GRCm38.p3 | 19:14569166 | TTAACCTGAGCTTTC[A/C]GAGTATAGGGTGGAA | 21888 |
rs30414690 | snp | G/T | 0.484429 | 0.0868505 | intron-variant | Tle4 | GRCm38.p3 | 19:14576379 | CAATTTTGGTCAGGA[G/T]GTAAATCAATTAGTT | 21888 |
rs30414754 | snp | A/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14574555 | ACAGCCTGTGTGTAA[A/T]GTGTGTTACTACTTA | 21888 |
rs30415478 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Tle4 | GRCm38.p3 | 19:14480910 | CTGAGCCCTACTCTG[C/T]GGCAGGCACTGTGCT | 21888 |
rs30417610 | snp | G/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14572658 | ACTACCTGGTATTCA[G/T]TCTCCAAGTATTTAT | 21888 |
rs30418421 | snp | C/G | 0.456747 | 0.140554 | intron-variant | Tle4 | GRCm38.p3 | 19:14577985 | TCATTACTGTGTTTA[C/G]AGAAAGCACTCAGAA | 21888 |
rs30425446 | snp | C/G | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14461243 | GGGGGGGGGGGGGGC[C/G]CTATTGTGGGTGGTG | 21888 |
rs30426596 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Tle4 | GRCm38.p3 | 19:14582098 | TATTCAAAAAAGTCA[C/T]AATGCGCCCAAGCAT | 21888 |
rs30444659 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | GRCm38.p3 | 19:14532194 | ACTTCTAGATTCCAA[A/G]TTGTGTTTCATTATT | 21888 |
rs30446462 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Tle4 | GRCm38.p3 | 19:14536294 | ACACAAGAAATTATC[A/T]CAGAAAAGTGGAAGA | 21888 |
rs30447526 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14544329 | GTTCATCTACTATTT[A/G]TCCTAAAAATGGACA | 21888 |
rs30454034 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14574694 | CAAGCAGGAATAGCA[A/G]GGGGCAGATTGTAGA | 21888 |
rs30455881 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14555779 | AGAGATGATATATAA[A/G]GGGTATGATCAAAAC | 21888 |
rs30503305 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14457772 | TGCCACACCCTGTCA[C/T]CCTCCAACATCCCCC | 21888 |
rs30512691 | snp | A/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14462982 | TGTCTCGAAAAAACC[A/T]AAATAAATAAATAAA | 21888 |
rs30512798 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14558374 | CTCCTTGATAAGCTA[C/T]AGTACAGCAAAATTT | 21888 |
rs30515572 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14525433 | AATCTCAACAGCGAA[C/G]TTCTCAAACACTATG | 21888 |
rs30518577 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14473135 | GAACTGTCCCCAGGT[C/T]CACTGAAAGAACAGT | 21888 |
rs30520970 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Tle4 | GRCm38.p3 | 19:14574723 | GAAAACCTGTGGCCT[C/G]GATACATGGTGTGGC | 21888 |
rs30545330 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Tle4 | Mm_Celera | 19:14457573 | CACAAAGATTCCAAA[C/T]TGATAACACCTCAAG | 21888 |
rs30554390 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14525571 | GAGCAAGAAATCTAT[C/T]CAGACAAACTGTATC | 21888 |
rs30555350 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14561790 | GAACTCACACACACA[C/T]ACACACACACACACA | 21888 |
rs30555668 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Tle4 | Mm_Celera | 19:14581463 | CACTATGTTTTAGAC[C/T]TTAGCTACTTAGAAA | 21888 |
rs30563468 | snp | A/C | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14593683 | ACAAAAAACAAAAAA[A/C]AAAAAAAAAAAACAC | 21888 |
rs30564028 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Tle4 | GRCm38.p3 | 19:14480943 | GCCCAAGACAACAGG[A/G]AAAAGAACAGGCAAA | 21888 |
rs30566930 | snp | C/G | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14583145 | CACTTGGGAGGCAGA[C/G]GCAGGTGGATTTCTG | 21888 |
rs30612622 | snp | G/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14529525 | ATAGAACCAACAGAT[G/T]CTCATGATCCTGATA | 21888 |
rs30614512 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14556305 | TCTTTCCTGATTTGG[A/G]GGAGGAAAATATTTA | 21888 |
rs30617509 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Tle4 | GRCm38.p3 | 19:14572961 | ATCATCTCCCAATGC[A/G]GTTCCATATCACACC | 21888 |
rs30619490 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14519416 | CCCTCCGTTAACCTA[A/G]CCTCGCACTCCATGC | 21888 |
rs30648924 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Tle4 | GRCm38.p3 | 19:14589579 | CCCGCTGGAGTTTAC[A/G]TTTAAGCATCAGAAT | 21888 |
rs30651608 | snp | A/G | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14529026 | TCTGTAGATCAGGCT[A/G]GCCTCAAACTCAGAA | 21888 |
rs30652807 | snp | A/T | 0.42 | 0.183303 | intron-variant | Tle4 | GRCm38.p3 | 19:14500191 | AAGTAGTGGGAAAAG[A/T]GGAGGAGTGGTATCA | 21888 |
rs30661465 | snp | C/T | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14487233 | TATTCTTTGTGTTAT[C/T]TCAAACATGAGAGGT | 21888 |
rs30666833 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14589478 | TATCAGTAATCTTAC[A/G]TTATAAAATGCTGCT | 21888 |