SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3683124 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Rhobtb1 | Mm_Celera | 10:69189201 | TTAGTAACATGACAA[A/G]AAGACAAGAATAGAA | 69288 |
rs3702150 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rhobtb1 | Mm_Celera | 10:69162651 | GGCGGGCTAAATTCA[C/T]CTGTCTCGGGTGTGT | 69288 |
rs6218121 | snp | C/T | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Rhobtb1 | Mm_Celera | 10:69218185 | CTCTCCTCCCAGCTC[C/T]TTTGTTCCACAGNCA | 69288 |
rs6218138 | snp | C/G | 0.231111 | 0.249285 | intron-variant, utr-variant-5-prime | Rhobtb1 | Mm_Celera | 10:69218198 | TCNTTTGTTCCACAG[C/G]CACCTTAGGGCAGAG | 69288 |
rs6218168 | snp | A/G | 0.48 | 0.0979796 | intron-variant, utr-variant-5-prime | Rhobtb1 | Mm_Celera | 10:69218219 | TAGGGCAGAGGTTGG[A/G]AAATCAGCCAATCAA | 69288 |
rs6218178 | snp | A/G | 0.48 | 0.0979796 | intron-variant, utr-variant-5-prime | Rhobtb1 | Mm_Celera | 10:69218225 | AGAGGTTGGAAAATC[A/G]GCCAATCAAGACACA | 69288 |
rs6325036 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Rhobtb1 | Mm_Celera | 10:69196450 | TCCTTCAATTCTCCT[C/T]AGCTTCAAATGTGAA | 69288 |
rs29313176 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rhobtb1 | Mm_Celera | 10:69173107 | AAATCAATACTAACT[A/T]ATATAGGGTTGTAGG | 69288 |
rs29314487 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69191589 | TGGCTATGAATCCCA[A/G]GAGTCTAAGACAAGG | 69288 |
rs29315040 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rhobtb1 | GRCm38.p3 | 10:69204010 | ATAGATAGATAGATA[A/G]ATAGATAGATAGATA | 69288 |
rs29316458 | snp | C/T | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69161748 | TTAATGAGTACATCA[C/T]CACCTCACAGGAGTG | 69288 |
rs29317957 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Rhobtb1 | Mm_Celera | 10:69161228 | TAACTCCTGCTACTA[C/T]GAGGAGCCTTCTGGT | 69288 |
rs29318053 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rhobtb1 | Mm_Celera | 10:69205213 | TGTACACCAGGGTAC[C/T]TAAGATTTGCTAGCT | 69288 |
rs29318069 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Rhobtb1 | Mm_Celera | 10:69289889 | GAAAGCTGACTGACT[C/T]TGAAGTCCTTCAACC | 69288 |
rs29318254 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rhobtb1 | Mm_Celera | 10:69222222 | GACCCAAAAGCATAT[C/T]GGGGAGGAAAGGATT | 69288 |
rs29318470 | snp | A/G | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69242564 | GTTTGGAAGGTGTAA[A/G]CTTCAACTAAGAAGA | 69288 |
rs29318640 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Rhobtb1 | Mm_Celera | 10:69264929 | CCACCCCCACTCCCC[A/C]GGCGTGGGCAAATAC | 69288 |
rs29320144 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rhobtb1 | Mm_Celera | 10:69203952 | GAGAAAGAGAGGGAT[A/G]TTGATAGATGGATGG | 69288 |
rs29321041 | snp | C/G | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69281171 | CAGGCTTCTCACATG[C/G]CGACATAAAATCCTG | 69288 |
rs29322272 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant, nc-transcript-variant | Rhobtb1, A930033H14Rik | Mm_Celera | 10:69212121 | AGCTGTCTCGTCTCG[A/T]TGCAGGACTAGAGTG | 69288 |
rs29322322 | snp | C/T | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69276352 | GAGCAGTTCTGAGGA[C/T]GCAGGGGACCAGGGC | 69288 |
rs29322368 | snp | A/G | 0.48 | 0.0979796 | intron-variant, downstream-variant-500B | Rhobtb1, A930033H14Rik | Mm_Celera | 10:69209161 | AACATCTCTTTTAGC[A/G]ATTAGTAGTTAAGGG | 69288 |
rs29322463 | snp | A/G | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69227871 | TCAACAGAAAGATGA[A/G]CGGCGGTCAAGGTGG | 69288 |
rs29322516 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rhobtb1 | Mm_Celera | 10:69265314 | CATTTTAACGTACCC[C/T]TGCCTGCCACCCACC | 69288 |
rs29322771 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69173672 | TTGTTCTGCCCCCCC[C/T]ACCCCACCCCATTCC | 69288 |
rs29322852 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Rhobtb1 | Mm_Celera | 10:69180738 | GAGACCATGGAAAAA[A/G]TAAAAGGTAAACAGA | 69288 |
rs29323828 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Rhobtb1 | Mm_Celera | 10:69280839 | CTGAAGTCATAGATC[C/T]AAACGAGTGTGTTAC | 69288 |
rs29325357 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Rhobtb1 | Mm_Celera | 10:69244278 | CATCACTCCGAGCAC[A/G]GGCACACTTGTCCTG | 69288 |
rs29325569 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69191288 | ATAGGATACAAAGCT[A/G]AAGGAAGCAGGAGCT | 69288 |
rs29326020 | snp | A/G | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69278545 | TCCATCTAGGACTTA[A/G]GCCTCAGGTCATTCC | 69288 |
rs29326315 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rhobtb1 | Mm_Celera | 10:69175771 | TGTCCATGCAGTTTG[G/T]TTTGATGATGTTTCA | 69288 |
rs29326387 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Rhobtb1 | Mm_Celera | 10:69252144 | AAAGAAGCATCAGTT[A/G]GGAATGAAGTTTTTG | 69288 |
rs29326705 | snp | A/T | 0 | 0 | intron-variant, utr-variant-5-prime | Rhobtb1 | Mm_Celera | 10:69218426 | ACAAGTTCCCAGTGT[A/T]TATGGGTTTTGATCT | 69288 |
rs29327420 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Rhobtb1 | Mm_Celera | 10:69279153 | GCCTCAGAACGGTGT[A/G]CCTGCAGTTGCCAGG | 69288 |
rs29327606 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69166737 | GTGGGGTGACGAATG[C/T]GTCTTTCTGCCTTCT | 69288 |
rs29327712 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Rhobtb1 | Mm_Celera | 10:69278756 | TGTGGGAGAAAGAAC[A/T]GAAGTATAGACAAAG | 69288 |
rs29327823 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69221160 | GACAGTCTGATTCAG[A/G]AGCTCTAAGGTAGGA | 69288 |
rs29328561 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Rhobtb1 | Mm_Celera | 10:69281003 | AAAAGGCAACTTGGA[A/G]CCAGATACTTTGAAC | 69288 |
rs29329960 | snp | C/T | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69263389 | CCTTCTTGAACTAGG[C/T]TAAAAAAAATGGGGG | 69288 |
rs29330644 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69192566 | CCCCCTACCCCCTCC[A/G]CAGCATAATAAACTG | 69288 |
rs29331069 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69241816 | GCCTTGTCACACTCC[G/T]TTTATCCCTCTGGAG | 69288 |
rs29331454 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rhobtb1 | Mm_Celera | 10:69222102 | ACACAGTGACGAGTC[A/T]GACAGAAGTGAAACC | 69288 |
rs29333328 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Rhobtb1 | Mm_Celera | 10:69226192 | AAATAGCGTGGCTGC[C/T]GATTGATTTCTGTAG | 69288 |
rs29333762 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rhobtb1 | Mm_Celera | 10:69166998 | CAAGTTCTTTTGCTT[C/T]CTCCTCAGCACTATC | 69288 |
rs29333875 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69168516 | CCCTCGGTTCTAGTA[C/T]GAGAGAACCCTCCTT | 69288 |
rs29333887 | snp | C/T | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69278656 | AACTAAAACAGAGTC[C/T]CCACATGTACCACAG | 69288 |
rs29335548 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rhobtb1 | Mm_Celera | 10:69205135 | ATGGTAAGTGTCCTG[C/T]AAGGGCCTTAGTGAT | 69288 |
rs29336038 | snp | A/T | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69278441 | GCCACACCTCCTAAA[A/T]GTGCCACTCCTCACG | 69288 |
rs29336140 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69286139 | TGTACATGCCCCCCC[A/T]CCCTGAAAACGAACA | 69288 |
rs29336776 | snp | A/G | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69278546 | CCATCTAGGACTTAG[A/G]CCTCAGGTCATTCCT | 69288 |
rs29336785 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Rhobtb1 | Mm_Celera | 10:69262323 | AAAGCAGCTTTTGAG[A/T]CTGCTGTTGAGTCTG | 69288 |
rs29337142 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Rhobtb1 | Mm_Celera | 10:69185472 | GCTTAATGGATGGGC[A/G]ATAGATGTACTGAAA | 69288 |
rs29337985 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rhobtb1 | Mm_Celera | 10:69269188 | GCATGCGCCACCACC[A/G]GGCTTATCAAGCGTT | 69288 |
rs29341388 | snp | G/T | 0.473373 | 0.11227 | intron-variant, upstream-variant-2KB | Rhobtb1 | Mm_Celera | 10:69265056 | CTGCATATATTTGTT[G/T]GCCCCCATTGATATG | 69288 |
rs29342877 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69221527 | CTGAATCTGGGACCC[C/T]GGAGCATGGGCTGAC | 69288 |
rs29343115 | snp | C/T | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69179137 | GGGTTCTGACAAGAG[C/T]GAGCAAGGTTGACCA | 69288 |
rs29343664 | snp | C/T | 0.42 | 0.183303 | intron-variant | Rhobtb1 | Mm_Celera | 10:69263065 | CTACCATTCTTTCTA[C/T]AACTGAAATAGACCC | 69288 |
rs29344329 | snp | A/T | 0.265928 | 0.249492 | intron-variant | Rhobtb1 | Mm_Celera | 10:69160021 | TAGTCTCCTGAATTA[A/T]GGTAGCCTGATGCAT | 69288 |
rs29345593 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69289120 | GATAAACCCCTTGGG[A/G]GGGGCCAGACTCGGT | 69288 |
rs29345800 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rhobtb1 | Mm_Celera | 10:69158978 | GGAAACATGGCATCC[A/G]CCAGCAGAAAACAGC | 69288 |
rs29345850 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69184246 | TCAGACACACCAGAA[A/G]AGGGCATCAGGTCCC | 69288 |
rs29346626 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rhobtb1 | Mm_Celera | 10:69272087 | AGCGATAGATGAACA[C/T]GGCTTGTATATGCCA | 69288 |
rs29348713 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rhobtb1 | Mm_Celera | 10:69248311 | CCTTTGTCATTGTCA[C/T]CTTAGCCATTATGAA | 69288 |
rs29349767 | snp | C/T | 0.32 | 0.24 | intron-variant | Rhobtb1 | Mm_Celera | 10:69289378 | AGCATAGAGTCTACA[C/T]ATTAGACTTTAGTCT | 69288 |
rs29349818 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69182510 | AGCAGAGGACCCCGG[C/G]ATTTTAGAGATGCCA | 69288 |
rs29350656 | snp | C/T | 0.32 | 0.24 | intron-variant | Rhobtb1 | Mm_Celera | 10:69159251 | GAAAGAAATGGCACC[C/T]TAAAATGAAGACAAG | 69288 |
rs29350959 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69184169 | AAAGCAATTGTATTT[G/T]TTTTTAGAGATTTAT | 69288 |
rs29351539 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rhobtb1 | Mm_Celera | 10:69205134 | CATGGTAAGTGTCCT[A/G]TAAGGGCCTTAGTGA | 69288 |
rs29352672 | snp | C/T | 0.277778 | 0.248452 | intron-variant, upstream-variant-2KB | Rhobtb1 | Mm_Celera | 10:69264862 | TGTGTAATTTGAGAA[C/T]ATCTTATTCTTAGGA | 69288 |
rs29354183 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Rhobtb1 | Mm_Celera | 10:69286921 | TATGTGCATGCGTGC[A/G]TAAGGTGCATTTGTA | 69288 |
rs29354338 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Rhobtb1 | Mm_Celera | 10:69182147 | ACAATGGATAGCTGG[C/G]CAGCTGGGGCTGAAG | 69288 |
rs29354389 | snp | C/T | 0.188366 | 0.242283 | synonymous-codon | Rhobtb1 | Mm_Celera | 10:69285718 | GGAGCTCACCAAGGC[C/T]GCTGTCAGTGGTGTG | 69288 |
rs29355563 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69173162 | GCCAGGGCAGGTACC[C/G]GGCTATAGGGAAGCA | 69288 |
rs29355930 | snp | G/T | 0.498615 | 0.0262793 | intron-variant, upstream-variant-2KB | Rhobtb1, A930033H14Rik | Mm_Celera | 10:69214970 | AATGACAATTTTTTT[G/T]AAGAAAATCTCCCAC | 69288 |
rs29356081 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Rhobtb1 | Mm_Celera | 10:69207210 | AGTGCATTTAAATAA[G/T]AAAAAATAAGAAAAT | 69288 |
rs29357144 | snp | A/G | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69247841 | CACACATGCACATGC[A/G]CACGCACGCGTGCAC | 69288 |
rs29357186 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rhobtb1 | Mm_Celera | 10:69223952 | GCTTTACAGCGCCTA[A/G]CTGCCTTCCCTTTGG | 69288 |
rs29357630 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69161616 | CAGGGGGGAAAAAAA[A/G]AAGAAGAAGAAGAAT | 69288 |
rs29357881 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Rhobtb1 | Mm_Celera | 10:69236322 | ACACAAAGCACGACT[A/C]TGATGCTCTTTCCCG | 69288 |
rs29358348 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Rhobtb1 | Mm_Celera | 10:69276123 | TAGCTAATTATAAGC[A/G]TGGAGATCACAGAAA | 69288 |
rs29358640 | snp | G/T | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69261600 | TGGTTCGGAAATTTT[G/T]CTGGAAAGAACCTAC | 69288 |
rs29359326 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rhobtb1 | Mm_Celera | 10:69268912 | ACTTCTTGCCTGTTT[C/T]TTCTCACTACAGAAA | 69288 |
rs29359868 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Rhobtb1 | Mm_Celera | 10:69289071 | GTAAGAGCATGTCTG[C/T]GAGCTCCCTGCCATC | 69288 |
rs29360191 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Rhobtb1 | Mm_Celera | 10:69288167 | TCAGAAAAGCTGGGT[A/G]GTGTATTCAGATTCC | 69288 |
rs29360238 | snp | A/G | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69279259 | CCCCAGGTCTCCCAC[A/G]TCCCATTTGAGCCCT | 69288 |
rs29360597 | snp | G/T | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69280188 | ATAAAATGAGTTAGA[G/T]AACAAGCCTTCCTAT | 69288 |
rs29360667 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Rhobtb1 | Mm_Celera | 10:69187112 | AGGGTAGCAGACTGA[C/T]TTGATATACGGAGGA | 69288 |
rs29361051 | snp | C/T | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69280760 | ATTCGTGTTTCTTCC[C/T]CAGTTTAAAAGAAAG | 69288 |
rs29361436 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69192686 | GAGACCCTGACTCAC[A/C]AAAAAAAAAAAAAAA | 69288 |
rs29364133 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Rhobtb1 | Mm_Celera | 10:69172857 | TCTCTGTATTAAATA[A/G]ACACAGGACTACTAG | 69288 |
rs29364581 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69226061 | CAGGAGCAGGCGTCA[A/G]TATACGCCTGTGACT | 69288 |
rs29364915 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Rhobtb1 | Mm_Celera | 10:69264898 | GCGTTTGCTATGTCT[A/G]GTGCAGTCCCCCCAC | 69288 |
rs29365830 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rhobtb1 | Mm_Celera | 10:69205065 | TTATATTAAAAGCAC[A/G]TTTGAAAGGCACTAC | 69288 |
rs29366406 | snp | C/T | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69179120 | CCTGGGGGAGGGGAG[C/T]GGGGTTCTGACAAGA | 69288 |
rs29366809 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Rhobtb1 | Mm_Celera | 10:69286211 | TTAGTATCCGTGTCT[A/G]TGATCCCTACACAAA | 69288 |
rs29368094 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69176698 | GGTGAGGAACAGGAA[A/T]GCTTCACTGGGGTTA | 69288 |
rs29368579 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69158643 | TCCCGTGAGAAATCA[C/T]GCCTAATAAAGCTAT | 69288 |
rs29368804 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69176697 | AGGTGAGGAACAGGA[A/G]TGCTTCACTGGGGTT | 69288 |
rs29370118 | snp | C/T | 0.5 | 0 | intron-variant | Rhobtb1 | Mm_Celera | 10:69203683 | AAGCCCATCACAGAC[C/T]ATGGTGGCCACTGTT | 69288 |
rs29370542 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rhobtb1 | Mm_Celera | 10:69191891 | AAGTTCTGTGACTCT[A/T]GAGAACCCTGACTAA | 69288 |