SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs251954410 | in-del | -/C | | | intron-variant | Tep1 | Mm_Celera | 14:50864456 | AGTACACTTAAATAG[-/C]ATATGTGTTCAGGGC | 21745 |
rs251962448 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50829353 | CTGCACTGATCGCTT[A/T]ATAGTGGTGCACTCC | 21745 |
rs251987150 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50848329 | TCTTCCCAAGGAAGG[C/T]TTCCATCACCCACAT | 21745 |
rs252082368 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50862019 | AAAGATAAATATTTT[A/T]AAAGCTTTATATGGA | 21745 |
rs252132366 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50842655 | GCTTCCTCACCATGA[G/T]GAACTATACCCGTGA | 21745 |
rs252173982 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50847981 | GATCATATAATGAGA[C/T]CCATCTCAAAAAGAC | 21745 |
rs252216775 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50834218 | GACAGTGAGTCACCA[A/G]AACGGGCAGAGGCCC | 21745 |
rs252251018 | in-del | -/GGAGAACACT | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839545 | TGCTGGTGCCGGACA[-/GGAGAACACT]GGAGAACACTGGAGA | 21745 |
rs252264787 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50848989 | TACAAGGAACACCAA[A/C]TGAGCTGAGCTAGTT | 21745 |
rs252272828 | in-del | -/ACACACAC | | | intron-variant | Tep1 | Mm_Celera | 14:50826255 | ACAAGTGCCCCCCAA[-/ACACACAC]ACACACACACACACA | 21745 |
rs252278148 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50859017 | TATCAACAGAGGCAC[C/T]GGTACAGAGAGACTA | 21745 |
rs252311742 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50850841 | GAAAGGAAAGTGCAG[C/T]TCCTGAGAATGCTTA | 21745 |
rs252312845 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50859812 | TCAAACCCAGAACCT[C/T]TTGAAGAACAACCAA | 21745 |
rs252371306 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50825752 | ACTTTAGTAGGTATC[A/C]GATTAGGATTTCTTA | 21745 |
rs252395713 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50856008 | TTGACCTTGCTTGGT[A/G]AAGGAAATTACCTAA | 21745 |
rs252423207 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50827688 | GACCAAGGAACTTTG[C/T]TTCTTGCCTTGTTTG | 21745 |
rs252560095 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50853811 | TTTAATACTAAATCC[C/T]CTCTCTCTCTCTCCT | 21745 |
rs252624341 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50858210 | TTGAGTAAGAATGGC[C/T]TCATAGGCTCATATA | 21745 |
rs252625676 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50855027 | TGAATGATGTGAAAG[A/G]GGGATTAACAGGAGC | 21745 |
rs252774498 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50825332 | ATGCATCAAGTGAAT[G/T]CATGTAAGATCTACC | 21745 |
rs252843931 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50826283 | ACACACACACACACA[C/T]ACACACACACACAAA | 21745 |
rs252876865 | snp | A/C | | | downstream-variant-500B | Tep1 | GRCm38.p3 | 14:50824034 | GTTGATCTAAAATCA[A/C]CAGCGAACACAATCG | 21745 |
rs252936723 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832182 | AACACGGGCTTTGGG[G/T]CTAGAAATGGCTACC | 21745 |
rs253049381 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50851851 | AGCCTCAGCTACAGT[A/T]GACAACAAAAAAGAG | 21745 |
rs253134420 | in-del | -/GTGTGTGT | | | intron-variant | Tep1 | Mm_Celera | 14:50856867 | TGTGTGTGTGTGTGC[-/GTGTGTGT]GTGTGTGTGTGAGAG | 21745 |
rs253185274 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50844200 | TGTGAAGAGGCCGGG[A/G]TCAGAAGTAGGGAAG | 21745 |
rs253227125 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50857984 | CTCTATCTTGAAAAT[-/A]AAAAGGGGGGAGGGG | 21745 |
rs253238530 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50834318 | AACTCAGTCAAGTGT[G/T]GCTCCGTGTGTATAA | 21745 |
rs253423632 | in-del | -/ACACATACG | | | intron-variant | Tep1 | Mm_Celera | 14:50839916 | CACAAACACACACAC[-/ACACATACG]ACATACACATACACA | 21745 |
rs253496967 | in-del | -/A | | | intron-variant | Tep1 | GRCm38.p3 | 14:50864981 | TAAGAACATCCCTCC[-/A]ATGGCTTCTGCATCA | 21745 |
rs253545533 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50848801 | TGTATATGTCTCTGT[A/G]TGGCAACCTAAACAA | 21745 |
rs253547538 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50870336 | CCAGCCGCCCGGAAG[A/G]ACTAAGCGGCTGCAC | 21745 |
rs253559838 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50833583 | CTGGGAAGGTAAGGA[C/T]AGGGCTTCTTCAGGA | 21745 |
rs253591901 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50828638 | ACTATAAAGGCACTA[C/T]TTTGGCTAACCTCCC | 21745 |
rs253616230 | in-del | -/CACACACACA | | | intron-variant | Tep1 | Mm_Celera | 14:50863063 | CTCAGCAGAACCCAC[-/CACACACACA]CACACACACACACAC | 21745 |
rs253656736 | in-del | -/TCAG | | | intron-variant | Tep1 | Mm_Celera | 14:50825234 | AAAGCTCTAAGACAG[-/TCAG]GATATATATGACACA | 21745 |
rs253658355 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50825662 | GGCCTGGCATTTGGG[A/G]ACTATGTATACTTCT | 21745 |
rs253685998 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50830368 | GACTGCACTAGTTTG[-/A]AAGTGTGCATACAGT | 21745 |
rs253689111 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50863886 | CATTCCAACATCTAA[C/G]AAGAACTCACTGATT | 21745 |
rs253760963 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50846363 | ACATCTGGTAGAGTC[A/G]TCTGCCAGCGTTTCA | 21745 |
rs253761545 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50861429 | AAGAAAGAAAGAAAG[A/G]AAGAAAGGAAGAAAG | 21745 |
rs253809522 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50836882 | TACAGACAGAGGGTC[C/T]GGGGGCCCCTAGTTC | 21745 |
rs253840855 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50827523 | CTTTTGCTTCCATCA[A/G]TAAGTTCTGCGGATG | 21745 |
rs253917232 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50827992 | ACAAAGAAACAAAAA[C/T]CACCAAATCCACCAC | 21745 |
rs254160481 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50839198 | GAAGCTAGTTTCAAa[A/G]agagagagagagaga | 21745 |
rs254290618 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839368 | GCGCACACCTTTAAT[C/T]TCAGTGCTTGGGGGG | 21745 |
rs254471587 | in-del | -/GTTGAGTT | | | intron-variant | Tep1 | Mm_Celera | 14:50866193 | CTGCAGAGGACCCAG[-/GTTGAGTT]CCTAGTACCCACATT | 21745 |
rs254483162 | snp | C/G | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869820 | TAGGATTAAGACATA[C/G]ACAGCCACATCTGGC | 21745 |
rs254505824 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50856746 | TAAACTCACAGAGAT[C/T]GACCTGACTCTGCCT | 21745 |
rs254594829 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50857221 | TTGAATCCCCAAATT[C/T]GTTACTCAATGCCAA | 21745 |
rs254596781 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50865397 | AAGAAAAATAAAAAA[A/G]GAAAGAAGAAAGCCA | 21745 |
rs254624712 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50846169 | CATTAAAAGCAGGAG[C/T]CAGATGACTTTTTGC | 21745 |
rs254638750 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50857768 | CTCTGGGTGACCACA[C/T]GCGGAAGCATGATTT | 21745 |
rs254763504 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50844065 | TGAAATCAGCTGCCC[A/G]TTACGATCCACCAAC | 21745 |
rs254788712 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50828405 | ACTGCTCTTCCAGAG[A/G]TCCTAAGTTCAATTC | 21745 |
rs254830186 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50832338 | TCACATGCACAAACC[A/C]AGAAAGATATATAAA | 21745 |
rs254932236 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869449 | AGTCTATGACTGTAA[C/T]CCCAACACTGAAAGG | 21745 |
rs254940243 | in-del | -/AAAC | | | intron-variant | Tep1 | GRCm38.p3 | 14:50852488 | TATAATCAATTAAAA[-/AAAC]AAAAACAAAAAACAA | 21745 |
rs255031211 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50860079 | AGGAGCCTTTCATAG[C/T]TAAAAATAGACAATC | 21745 |
rs255034721 | in-del | -/T | | | intron-variant | Tep1 | Mm_Celera | 14:50829841 | CACCTTCTCTATCGC[-/T]TCCCCACTCCAGTTC | 21745 |
rs255069611 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50860506 | ATCTAAAATACAGGC[A/G]TAGGAAGGGAGAAGT | 21745 |
rs255129066 | snp | A/G | | | synonymous-codon, utr-variant-3-prime | Tep1 | Mm_Celera | 14:50831765 | CACGGCACTCTGGTG[A/G]CCTGAGAACTGGCCA | 21745 |
rs255131188 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50855520 | GACTGCTTCAGGCAT[A/G]TGGAAGAGTCTGGCC | 21745 |
rs255169713 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50850026 | TCCGATGCCCAATGT[A/G]GACTCACTTCAGGAT | 21745 |
rs255233451 | in-del | -/TCGC | | | intron-variant | Tep1 | Mm_Celera | 14:50857735 | CAGCTCCATCCGTGT[-/TCGC]TCTGGCCTTTCTGTG | 21745 |
rs255250196 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50824765 | CTTTAAATTTGTGGG[A/G]TCAATCCAGCAATCA | 21745 |
rs255429664 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50857674 | GAAACATGAATTCGG[C/T]TGTGGAGCTAAATCG | 21745 |
rs255430599 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855484 | CTCTTACATCCCACA[C/T]AGAAACAAGCTGGTA | 21745 |
rs255506343 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50847667 | CTCCTCCAGCGGCCG[A/G]AGAGACGGTGCCTGT | 21745 |
rs255518165 | in-del | -/GAACAA | | | intron-variant | Tep1 | Mm_Celera | 14:50863097 | CCTAGAGTTACATAG[-/GAACAA]GAACAAGAACAATTT | 21745 |
rs255568741 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50868917 | GGTCGGTATTGCAGT[A/G]TTGTACAGCCATCAC | 21745 |
rs255606543 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50825603 | CTGAGAATTGCATGT[C/T]CAGGTTGGGCTATGT | 21745 |
rs255674472 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50860457 | ATTAAGTTGAAAATT[A/C]ACTGCACCATTTTGT | 21745 |
rs255706991 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50840402 | AACTGAGAAAGTCTA[C/G]TGAAGAGGTCTAAGC | 21745 |
rs255718919 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50839802 | GGATTAAAGGCGTGC[A/G]CCACCACTGCCCTGC | 21745 |
rs255719041 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50850900 | GGTGGCATCAAAGAA[C/T]CAGGGACAGCAGGGA | 21745 |
rs255758174 | snp | A/G | | | intron-variant, downstream-variant-500B | Tep1 | Mm_Celera | 14:50840821 | AAAGAACCGGAGGGA[A/G]GACAGCAGGAAAAGT | 21745 |
rs255843199 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50857655 | AAAAAAAGAAACAAA[A/G]AGGGAAACATGAATT | 21745 |
rs256186090 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50825535 | TTGCAGAAGGACATG[C/T]CTGTATTTCCCTACT | 21745 |
rs256187899 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855751 | ACACATACAAAGTTA[C/T]AGTCCCCAGCAGGAA | 21745 |
rs256232346 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50830688 | CTGTATCACTATTTG[C/G]TGTGCACATAATTAA | 21745 |
rs256232695 | snp | C/T | | | synonymous-codon | Tep1 | Mm_Celera | 14:50844942 | ATAGGGCCGGCCAGC[C/T]GCTACACCTCCCCAT | 21745 |
rs256403133 | in-del | -/TTTC | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871219 | AAACCCTTTTGATTG[-/TTTC]TTTCTTTCTTTTTCA | 21745 |
rs256446472 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50867200 | TTCCCCAGAAGCCCC[A/G]AGCTTCTTCATTCAC | 21745 |
rs256514316 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50833805 | TAGACCTGCCTGCAG[C/T]TCTGGTAGATCAAAA | 21745 |
rs256536758 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50858871 | TCAGTCCCCAATCAC[A/T]ATGATTACAAGTGTG | 21745 |
rs256600296 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50834605 | ACATAGCATTGTAAT[A/G]TTTATTCCAAATCTC | 21745 |
rs256635170 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50827023 | CTCTTTTCTTCTTTT[C/T]AACACAAGAGGAAAA | 21745 |
rs256688402 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50829816 | AGGAGGGCTGCAGAG[C/G]TTGCCCTGTACACCT | 21745 |
rs256787926 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50841734 | AACCCTCTGGCAGCT[A/C]AAACCACACAGGGAG | 21745 |
rs256826102 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50861905 | TGACTCACAAATGTC[G/T]GTAACTCTAATCCCA | 21745 |
rs256845308 | in-del | -/CAC | | | intron-variant | Tep1 | Mm_Celera | 14:50852325 | CCGTGTGTGTTTCCA[-/CAC]CACATCTCCTGCCCT | 21745 |
rs256860358 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50862566 | GTTCTGTCTTCTACA[A/G]GGAGGAATAGGAGAA | 21745 |
rs257057688 | snp | G/T | | | intron-variant, downstream-variant-500B | Tep1 | Mm_Celera | 14:50831512 | GAGGGATGCAGAACT[G/T]TGGAGTTGAGTGGCT | 21745 |
rs257112065 | snp | A/C | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871749 | TACCCTTATAATTCC[A/C]GAGATTTTAAAGGCT | 21745 |
rs257118105 | in-del | -/TTC | | | intron-variant | Tep1 | Mm_Celera | 14:50830397 | GTTGTCTTGTAATAA[-/TTC]TTCTCCTGGCAGCCT | 21745 |
rs257241818 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50834888 | GGGAAAAAACATCTG[A/C]AGCAGAGAGAGCTAG | 21745 |
rs257455450 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855452 | CTGTCTTTCCCAACA[C/T]CTGTAGGTTTTCACA | 21745 |
rs257469687 | in-del | -/AGCAAGCAC | | | intron-variant | Tep1 | Mm_Celera | 14:50854115 | AATTTCCCCCCAGCT[-/AGCAAGCAC]ATACCTGGCCTTGTG | 21745 |
rs257488682 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50828243 | TATCTAGGAGTACAC[A/G]GAAACTCTGTCTTGA | 21745 |
rs257492147 | in-del | -/AC | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839906 | CACAGAGACACACAA[-/AC]ACACACACACACATA | 21745 |
rs257511866 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50825184 | GGGATAGGTAGAGAG[C/G]TAACTTTGTTTAGTT | 21745 |
rs257521996 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50837333 | GTCATGCCACGTGGA[A/G]CAACAAAATCAGTTT | 21745 |
rs257837955 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50840189 | GGACTCCATTAACTT[C/T]AGCACCAAGTATAAT | 21745 |
rs257931313 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50831216 | GACACACATGGTATT[A/G]GGAATTGATCTCAGG | 21745 |
rs257955119 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50866511 | ATAAATAGGTACAGA[A/G]AATGTGGACCAAGGT | 21745 |
rs257963593 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50825549 | GTCTGTATTTCCCTA[C/T]TTATCATGTTCTACT | 21745 |
rs257987132 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50828013 | AATCCACCACAGCTT[C/T]AGCACTGGCTGGAAT | 21745 |
rs257994782 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50858389 | GCCTCCCCCACTGCC[C/T]CCCTCCCCCTTTTAC | 21745 |
rs258028519 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50828810 | TGACATCCTCTCACA[G/T]CCTTGCCCGAAAGCA | 21745 |
rs258034891 | in-del | -/CCTTTATTTAGA | | | intron-variant | Tep1 | Mm_Celera | 14:50826619 | TACAACTCTGTTTTG[-/CCTTTATTTAGA]CACAATGAAATCTTA | 21745 |
rs258119587 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50829099 | CCCCTCCGACATGCA[G/T]GCAAAACTCCAGCCC | 21745 |
rs258182909 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839395 | GGGGCAGAGGCAGGT[A/G]AATTTCTGAGTTCGA | 21745 |
rs258402571 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50858543 | CACTCACATCTACAA[G/T]TAAATGCTTTCTTCT | 21745 |
rs258456587 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50838199 | ACTCAAAGGGAAGCC[A/G]CACAGTCATGGTGCA | 21745 |
rs258489104 | in-del | -/TATA | | | intron-variant | Tep1 | Mm_Celera | 14:50827417 | ACTCTAGCACTGAGC[-/TATA]TATATTCCCAACACC | 21745 |
rs258496407 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50849776 | GAGTGACAGTGGACT[C/T]ATACACATGGACTAA | 21745 |
rs258544946 | snp | A/G | | | synonymous-codon | Tep1 | GRCm38.p3 | 14:50839032 | GAGCAGGGGGGCCTG[A/G]CAGCAAACAGGTGAC | 21745 |
rs258652224 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50870867 | GAAAGAAAGATCGCT[A/G]AGAGTGTGCCCTTGG | 21745 |
rs258718325 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50846143 | GTGAAAACCATTAAA[A/G]CCATTAAAACCATTA | 21745 |
rs258809432 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872336 | GGATGATGAGTCTAC[A/G]ATTCTTACCACAAGA | 21745 |
rs258856097 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50861699 | ACAAGGCAGGAATGA[A/G]AACGTAGAAGATCCT | 21745 |
rs258917999 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50842383 | GACTCGGGTTTAACT[C/T]CCAGACCCACATGAT | 21745 |
rs258938428 | in-del | -/TTGT | | | intron-variant | Tep1 | GRCm38.p3 | 14:50859556 | CAACATAGAGAGAAA[-/TTGT]TTGAATTTCCAAAGA | 21745 |
rs258975184 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855300 | CACAGAGCCCCATTG[C/T]TTTTTATATTACACT | 21745 |
rs259050222 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50825929 | GCTAATACTGACAGA[A/G]ACCAAAAAAAAAAAA | 21745 |
rs259061932 | snp | A/C | | | intron-variant | Tep1 | GRCm38.p3 | 14:50859428 | AATGAGGCCACACCC[A/C]CTCCAACAAGGCCAC | 21745 |
rs259285984 | in-del | -/CG | | | intron-variant | Tep1 | Mm_Celera | 14:50863922 | TGGGTGCGTTGTAAA[-/CG]TGAGAGAAATAACAG | 21745 |
rs259408717 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50866269 | GACAGATGCAGGGGG[A/C]AGTCTCAGTTTGTAG | 21745 |
rs259472509 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50847420 | ACAGACATTTTTTTT[C/T]TCTCTCTAGTAAAGC | 21745 |
rs259488894 | snp | G/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839451 | TCCAGGACAGCCAGG[G/T]ATACACAGAGAAACC | 21745 |
rs259508462 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50845304 | CTAGAGTCGGAGTGG[-/A]AAAAAACGGATCTGA | 21745 |
rs259579534 | in-del | -/G | | | intron-variant | Tep1 | Mm_Celera | 14:50826432 | AACAACTGGAAAGGA[-/G]GAAGGAAGGAAGGAA | 21745 |
rs259600148 | snp | C/G | | | synonymous-codon, intron-variant | Tep1 | Mm_Celera | 14:50841280 | TTTAATTGTTGTCCT[C/G]AGGGGCCCATCAGAG | 21745 |
rs259678517 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50832500 | TGGGAATTGAACTCA[A/G]GAAGAAGCAGCCAGT | 21745 |
rs259743671 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50867805 | CCTACCTACCATGTG[C/T]ATGCCTCTGGGTTCA | 21745 |
rs259804876 | in-del | -/AGT | | | intron-variant | Tep1 | Mm_Celera | 14:50826178 | ATCTCTAGATCAAAC[-/AGT]AGAAGAAGAGAACCA | 21745 |
rs259926514 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50825529 | CTTCCTTTGCAGAAG[A/G]ACATGTCTGTATTTC | 21745 |
rs259959905 | snp | A/T | | | missense | Tep1 | Mm_Celera | 14:50844599 | TCCCATGGGGCAGCA[A/T]CAGCTGCTGCACTGT | 21745 |
rs259992247 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50870250 | CCCTCCTAGGATTCT[C/T]TAAGGCAAAAGGAAC | 21745 |
rs260058304 | snp | A/T | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823563 | GATCCATCTCTCAGC[A/T]CCATGAACTTCAATT | 21745 |
rs260106293 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871589 | TTGGTAACTCTAATT[A/G]CCCATGGTGACCTCT | 21745 |
rs260142501 | snp | C/G | | | downstream-variant-500B | Tep1 | GRCm38.p3 | 14:50824037 | GATCTAAAATCACCA[C/G]CGAACACAATCGGGC | 21745 |
rs260160177 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50842585 | TTCATGATATTTTTA[A/G]AGTAAGGAAGCTGAG | 21745 |
rs260173157 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832171 | ATCGTGTTAGGAACA[C/T]GGGCTTTGGGGCTAG | 21745 |
rs260356148 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50845086 | AACCTCTTTCTGTTC[A/G]TGTAGATATCTCTTC | 21745 |
rs260472842 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50837774 | CATTGCAGGCCCCAG[A/C]CATAAAAAGGGGTTT | 21745 |
rs260480474 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50827205 | CAGATGAAGACTGTA[A/G]TGCAGAAGACACACA | 21745 |
rs260564235 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50845726 | TGGGTATTTTTTTTT[A/T]AAGATTTATTTATTA | 21745 |
rs260671740 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855814 | ATGCAATCTGCTCTA[C/T]TCAAAAGATTTTAAA | 21745 |
rs260700048 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50856595 | GAGAGAACTGATTAC[C/T]ACAAGTTGTCCTTTG | 21745 |
rs260797947 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50857156 | TGACCTCTACACTTT[G/T]CAGTGATCTAATATT | 21745 |
rs260829185 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50846672 | ACAGAGGCGGCAGGG[C/T]CCTGAATCGAACTGG | 21745 |
rs260987455 | snp | A/G | | | missense | Tep1 | Mm_Celera | 14:50868186 | GACCCTGGAGCAAGG[A/G]GCTGGTCAATGCAGT | 21745 |
rs260991776 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50858844 | TGATCTCAAACTAGT[C/T]CTCCTCCTGCCTCAG | 21745 |
rs261071913 | in-del | -/C | | | intron-variant | Tep1 | Mm_Celera | 14:50840301 | ACAAAGCTCTGGGTT[-/C]CACTGAAGACCTAGG | 21745 |
rs261117028 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50853677 | GCTGTTTCCAGGGCC[C/T]GGCGATAGCGCTCCA | 21745 |
rs261210971 | in-del | -/C | | | intron-variant | Tep1 | Mm_Celera | 14:50839656 | AGTAAGAGACCTTTT[-/C]TCTCTTTTGTTTTTG | 21745 |
rs261229421 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50858479 | GGCATGCCACCATGC[A/T]TCCCTTCATGGTAAT | 21745 |
rs261238408 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50866907 | ATTGCACCACGAATG[C/G]ATGCACAGCCCTCCA | 21745 |
rs261294624 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50862063 | TGACATTTTAAATTC[A/T]TGGATCCAGCTGGAT | 21745 |
rs261330136 | snp | G/T | | | missense | Tep1 | Mm_Celera | 14:50855617 | TCTCTGGAGAACGAG[G/T]TCATGGTGGCGGGCA | 21745 |
rs261423267 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50845819 | CGGGTGGTTGTGAGC[C/T]ACCATGTGGTTGCTA | 21745 |
rs261445488 | in-del | -/TGT | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | GRCm38.p3 | 14:50872218 | AGAAATAAATGTGTG[-/TGT]GGGGGGGAGAGAGAG | 21745 |
rs261728508 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50858006 | GGGGAGGGGTAGAGA[A/G]ATGTCTGAGCAGTTA | 21745 |
rs261771190 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50827737 | TAAGAACTGACTCTA[C/G]CTGGGCGTGGTGGCG | 21745 |
rs261850430 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50825607 | GAATTGCATGTCCAG[A/G]TTGGGCTATGTTGAA | 21745 |
rs261886193 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50860358 | GATCGACCTATGATA[G/T]CAACACTATTTAAAG | 21745 |
rs261929856 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50852885 | GGGTGTGTTCTATTA[A/C]ACCTGGCTACTCATG | 21745 |
rs261987973 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855508 | GCTGGTAGCCATGAC[C/T]GCTTCAGGCATGTGG | 21745 |
rs261991753 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50826183 | tagatcaaacagtag[A/G]agaagagaaccaacc | 21745 |
rs262135229 | in-del | -/AGAG | | | intron-variant | Tep1 | GRCm38.p3 | 14:50835437 | GAGACAGAGAGAGAC[-/AGAG]AGACTGTCTCAATGA | 21745 |
rs262204347 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50866873 | CACCATTGACCCTAC[A/G]AACAGTGGCTGTTAT | 21745 |
rs262229063 | in-del | -/AGAGAGAGAGAGAGAGAGAG | | | intron-variant | Tep1 | Mm_Celera | 14:50839197 | AGAAGCTAGTTTCAA[-/AGAGAGAGAGAGAGAGAGAG]AGAGAGAGAGAGAGA | 21745 |
rs262294363 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50829394 | GCACTAGGGACACAG[A/T]GGAAGGTACATCTCT | 21745 |
rs262305737 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50837896 | CATAGCACAGATTTT[C/T]GGGGCTCTAGGGAAA | 21745 |
rs262326177 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50828560 | GATCCCCAGAACCCA[C/T]ATGCTGGTAAGGTGA | 21745 |
rs262390872 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50863279 | ATTAATTAAAAAAAT[A/G]AAGAAAGTCCAGAAT | 21745 |
rs262398131 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50824215 | GTGTGTCTCCCACAG[C/T]AAGCTGCAGGGGAGA | 21745 |
rs262456690 | in-del | -/AGA | | | intron-variant | Tep1 | Mm_Celera | 14:50826181 | TCTAGATCAAACAGT[-/AGA]AGAAGAGAACCAACC | 21745 |
rs262586623 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832087 | GATTAGTTTTATGCC[G/T]TAGGAGCAAATAAAT | 21745 |
rs262646881 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50827895 | GAAAAAAAAAAAAAA[A/C]ACTGAACTGATTCTA | 21745 |
rs262676932 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50865562 | GTGGCTTTTGTTTAG[A/G]GTAACTTACTGCAGG | 21745 |
rs262727700 | snp | A/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871377 | CCAACCACCACGCCC[A/T]GCAACAAATTTTTTT | 21745 |
rs262743541 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50834915 | CTAGAATAATACTAA[A/C]CTGCAAGTATCATGG | 21745 |
rs262748908 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50861289 | AGCGTCAGCAACTTG[A/G]GAGACTAAGGCAAAA | 21745 |
rs262821262 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50833267 | CTACTTTACAGGGCA[C/T]AGTAAAGATTAACTG | 21745 |
rs262958210 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50864660 | TATATGTAAGTATAT[A/G]TATATAAAATTGAGA | 21745 |
rs262976048 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50857243 | CAATGCCAAGTGCTC[A/C]GCCTTGAAATCATGT | 21745 |
rs263041408 | snp | A/T | | | missense | Tep1 | Mm_Celera | 14:50841599 | AATGGACACAAGGGG[A/T]AAGGGTTTCCACTGT | 21745 |
rs263086931 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832683 | ACCCTTTCACGGGGT[C/T]ACATATCAGATATCC | 21745 |
rs263136762 | snp | C/T | | | synonymous-codon | Tep1 | Mm_Celera | 14:50836389 | TGGGTTGAGAGCCAC[C/T]GAGAGTGCAGGAGAA | 21745 |
rs263218425 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50860876 | TGGAGCCATGAATGA[G/T]CCAGAATGACCAGGT | 21745 |
rs263409636 | snp | C/G | | | missense, downstream-variant-500B | Tep1 | Mm_Celera | 14:50840627 | GGACTAGACCCACTT[C/G]CAGATATGCAGCAAC | 21745 |
rs263451452 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50865701 | ATCCAAGTTTCATCA[A/T]GTTAACAAGACTCCC | 21745 |
rs263516214 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50838180 | CAAAAGACTAAGTCA[C/T]ACGACTCAAAGGGAA | 21745 |
rs263646726 | snp | A/C | | | missense | Tep1 | Mm_Celera | 14:50845535 | CCCTGAAGGGTACTC[A/C]TGGGTCTGCATGGAG | 21745 |
rs263673355 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50837287 | ATCTTATCTAGTCCC[C/T]TGATTCAGCAAGGCT | 21745 |
rs263690159 | snp | G/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872218 | AGAAATAAATGTGTG[G/T]GTGGGGGGGAGAGAG | 21745 |
rs263835963 | in-del | -/ATACAGAACT | | | intron-variant | Tep1 | Mm_Celera | 14:50866109 | AGAAGAAAGGAGTAA[-/ATACAGAACT]ATACAGACCAACTTG | 21745 |
rs263837122 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50839762 | CGAACTCAGAAATCC[A/G]CCTGTCTCTGCCCCC | 21745 |
rs263887286 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50836648 | TCCCTACTTTTGCTA[A/C]TCTGTCCCAGAACCC | 21745 |
rs264005254 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50842619 | CATTCATCCTCTGAT[C/T]CCTGATTCAAGCTCC | 21745 |
rs264030186 | in-del | -/GAGAGAGAGAGAGAGAGAGT | | | intron-variant | Tep1 | Mm_Celera | 14:50839214 | AGAGAGAGAGAGAGA[-/GAGAGAGAGAGAGAGAGAGT]GAGAATAGCTGAGGA | 21745 |
rs264126878 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50846901 | AAGACTGATGCGGTG[A/G]GGGAACACTCTGGCC | 21745 |
rs264128142 | in-del | -/AGAC | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823608 | TTTGTGATCTCTGTA[-/AGAC]AGAGTGCCAATTAGT | 21745 |
rs264134428 | snp | A/G | | | intron-variant, utr-variant-3-prime | Tep1 | Mm_Celera | 14:50841089 | TGAGAAGGGCTTCCC[A/G]CTGCAGCATATCCGA | 21745 |
rs264188433 | snp | C/G | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50824010 | AAAGGAATATCCAGA[C/G]CCCTCCCCGTTGATC | 21745 |
rs264309890 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50851090 | CTTGTTTTTGAGGAT[C/T]TCTGTGTAGTCCTGT | 21745 |
rs264332091 | snp | G/T | | | intron-variant, downstream-variant-500B | Tep1 | Mm_Celera | 14:50840879 | TAAATGACACGGGTG[G/T]GGTTGGTGTGAAAGG | 21745 |
rs264407326 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50854617 | GTAAAACAAGAAGGA[C/T]GGTGAGCAGAGGAGG | 21745 |
rs264454357 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50843062 | AAAGCCTTCCTTCCC[A/G]AGGCAGGCTGCTTGT | 21745 |
rs264610536 | in-del | -/ACAT | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839511 | CAGCCAGGTGTGGCC[-/ACAT]GCACCTGTAAGCCCA | 21745 |
rs264727165 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50857376 | GAAGGGTTGGAGGAA[A/G]GAAAGGAAAAAGGGA | 21745 |
rs264750572 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50847390 | TCGATGTGGAGTCTT[C/T]TCTCCTCCCTACATA | 21745 |
rs264851859 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50860618 | TTTGTTTCCCCGTAA[A/G]CTCAGCTCCCGCTCC | 21745 |
rs264861799 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50853887 | AGAGCCTTTCCTTTT[C/T]CTCCATACCACAGGA | 21745 |
rs264906834 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50855790 | CCACACAGAAGCTCA[A/G]ATGGGAGAATGCAAT | 21745 |
rs264915882 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50845034 | ACGCCTCTAACGGAG[A/G]GGTGCCTCGGCCTCC | 21745 |
rs264927415 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50826077 | GAGTCCCCAGACAGG[A/G]CAGCAAGAGCTGCAC | 21745 |
rs264985806 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50858189 | GCAAAACTCCCTTGA[A/G]GTGGTTTGAGTAAGA | 21745 |
rs265109928 | snp | A/C | | | missense | Tep1 | Mm_Celera | 14:50824916 | GATAAGTTCCACAGC[A/C]TCCCATCAGAGGTGG | 21745 |
rs265191385 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50827291 | ATGAATGAAGTATAA[A/C]GCACAAGGACTGCCC | 21745 |
rs265291053 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50836779 | GGGAAGGCCGCCAGC[C/T]GGGCACCCTCTTGCC | 21745 |
rs265356231 | in-del | -/GACC | | | intron-variant | Tep1 | Mm_Celera | 14:50855555 | GGTGCACAGTCTCCT[-/GACC]GAGCCACACACTCCC | 21745 |
rs265387376 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50856643 | CCTCACACACAAATA[A/T]ATAAGTATAACCTTC | 21745 |
rs265455925 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50865018 | GCTTCATGACCTGCT[G/T]AGTTCCAGTCCTGAC | 21745 |
rs265495942 | snp | G/T | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | GRCm38.p3 | 14:50869567 | AGTCTCCACATACCC[G/T]TATATATATCCGCAT | 21745 |
rs265526089 | snp | A/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871691 | AGTGGAGTGTGTGGG[A/T]GGAGGTCTGTTTTGT | 21745 |
rs265547908 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50861820 | AAGGGGCTGGAGAGA[C/T]TACTCAATTGTAAAA | 21745 |
rs265570919 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50833728 | GAGATTAAGGTAGGT[A/G]CCACCACACCAGGTT | 21745 |
rs265630766 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50864985 | AACATCCCTCCAATG[C/G]CTTCTGCATCAGCTC | 21745 |
rs265668682 | in-del | -/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839552 | GCCGGACAGGAGAAC[-/T]ACTGGAGACAGGAGA | 21745 |
rs265685054 | in-del | -/G | | | intron-variant | Tep1 | Mm_Celera | 14:50859045 | CTATTACATAGCAAA[-/G]CAATTCAGGCTGCCT | 21745 |
rs265749348 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50831929 | TCTCACTCACTATGA[A/G]GCACTGGTTGGCCTG | 21745 |
rs265797719 | in-del | -/CTAAA | | | intron-variant | Tep1 | Mm_Celera | 14:50866971 | GAAAGGTCCAAATCT[-/CTAAA]CTAATAAACCCTCTC | 21745 |
rs265799775 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839369 | CGCACACCTTTAATT[C/T]CAGTGCTTGGGGGGC | 21745 |
rs265843322 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50834733 | TGGACTTCTCCCAGC[C/T]AGGGGAGGAGGGAGA | 21745 |
rs265969956 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50846027 | TTGTGTGTGTGTGTG[G/T]GGGGGGGGGTCCTCA | 21745 |
rs266181735 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871015 | GCTTTGCCACAGGCC[A/G]AAGCAAGAGGGTCAA | 21745 |
rs266221867 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50841488 | TGGGGCTTTACCGAA[A/G]GACGGGTGGGATGAA | 21745 |
rs386835041 | in-del | -/AA | | | intron-variant | Tep1 | Mm_Celera | 14:50849846 | AAAAGTGCTCTATTT[-/AA]AAAAAAAAAAAGGCA | 21745 |
rs386862992 | in-del | -/C | | | intron-variant | Tep1 | Mm_Celera | 14:50825020 | TCCCCTAAGCCACCC[-/C]AGAAAGAGCACTCTG | 21745 |
rs386906958 | in-del | -/TT | | | intron-variant | Tep1 | Mm_Celera | 14:50851016 | TTTTGGGTTTTTTTT[-/TT]GGTTTTTTAAATTTT | 21745 |
rs386935809 | in-del | -/CA | | | intron-variant | Tep1 | Mm_Celera | 14:50839919 | AAACACACACACACA[-/CA]TACGACATACACATA | 21745 |
rs386947605 | in-del | -/T | | | intron-variant | Tep1 | Mm_Celera | 14:50845726 | TGGGTATTTTTTTTT[-/T]AAGATTTATTTATTA | 21745 |
rs386992383 | in-del | -/T | | | intron-variant | Tep1 | Mm_Celera | 14:50857127 | TGTAATTTTTTTTTT[-/T]AAAGGAAGAGTAGTG | 21745 |
rs387017324 | in-del | -/GA | | | intron-variant | Tep1 | Mm_Celera | 14:50826550 | AGAAAGAATGAAAGA[-/GA]AAGGAAGAACGAAGG | 21745 |
rs387034875 | in-del | -/AA | | | intron-variant | Tep1 | Mm_Celera | 14:50863927 | GCGTTGTAAATGAGA[-/AA]GAAATAACAGGCTGA | 21745 |
rs387070088 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50861433 | AAGAAAGAAAGAAAG[A/G]AAGGAAGAAAGGAAG | 21745 |
rs387110067 | in-del | -/CGCCGCCGCCGCCGCCGC | | | intron-variant | Tep1 | Mm_Celera | 14:50828879 | CTTGCCATGCGCAGC[-/CGCCGCCGCCGCCGCCGC]AGCCGCCGCCGCCGC | 21745 |
rs387110593 | in-del | -/GAG | | | intron-variant | Tep1 | Mm_Celera | 14:50834829 | GAGGAGGAGGAGGAG[-/GAG]AAGAGAAGCAAGCCA | 21745 |
rs387144661 | in-del | -/TTT | | | intron-variant | Tep1 | Mm_Celera | 14:50839680 | TTTTTGTTTTTTTTT[-/TTT]CCGAGACAGGGTTTC | 21745 |
rs387167482 | in-del | -/GTATATATATCCGCATATGCACATACTC | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | GRCm38.p3 | 14:50869567 | AGTCTCCACATACCC[-/GTATATATATCCGCATATGCACATACTC]TTGCACACACAAACA | 21745 |
rs387173123 | in-del | -/GTGTGTGTGTGT | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50868754 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGT]ATTGAGAGAGGGAGA | 21745 |
rs387176715 | in-del | -/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50845717 | AACAGGTACTGGGTA[-/T]TTTTTTTTTAAGATT | 21745 |
rs387244024 | in-del | -/C | | | intron-variant | Tep1 | Mm_Celera | 14:50847321 | CAATCAAGCAAGCCC[-/C]ATGTGAAAAGCCAGA | 21745 |
rs387251452 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50842124 | AGGTTAAAAAAAAAA[-/A]CAAAAAACAGGAAAG | 21745 |
rs387364221 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50857646 | TCTTTAAAAAAAAAA[-/A]GAAACAAAAAGGGAA | 21745 |
rs387399879 | in-del | -/CTGGCTC | | | intron-variant | Tep1 | GRCm38.p3 | 14:50838144 | GTGAACAACTGGATC[-/CTGGCTC]TCAGCCCTGTTCCTC | 21745 |
rs387421809 | in-del | -/A | | | intron-variant | Tep1 | GRCm38.p3 | 14:50867951 | AACAGAACATATAGC[-/A]AAAAAAAAGGCTAGA | 21745 |
rs387427489 | in-del | -/GAGAGAGA | | | intron-variant | Tep1 | GRCm38.p3 | 14:50852757 | AGAGGCAGAAAGAGA[-/GAGAGAGA]CAGAGAGACAGAGAG | 21745 |
rs387457558 | in-del | -/TGT | | | intron-variant | Tep1 | Mm_Celera | 14:50830384 | AAGTGTGCATACAGT[-/TGT]CTTGTAATAATTCTT | 21745 |
rs387461047 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50861441 | AAGAAAGAAAGGAAG[A/G]AAGGAAGAAAGGAAG | 21745 |
rs387476709 | in-del | -/GTATGTATGTAT | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869699 | TATGTATGTATGTAT[-/GTATGTATGTAT]TGAAACAAGGTCTCA | 21745 |
rs387485898 | in-del | -/ATAA | | | intron-variant | Tep1 | Mm_Celera | 14:50866489 | GGCATAAATAAATAA[-/ATAA]TAAATAAATAGGTAC | 21745 |
rs387497254 | in-del | -/GTGTGTGTGTGTGTGTGTGT | | | intron-variant | Tep1 | Mm_Celera | 14:50842517 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGTGTGT]TGAACACTCACACAT | 21745 |
rs387502096 | in-del | -/CC | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50868958 | CTTGCTGCCCCCCCC[-/CC]TTTTAGATTTATCCA | 21745 |
rs387628841 | in-del | -/CAGA | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823611 | GTGATCTCTGTAAGA[-/CAGA]GTGCCAATTAGTCTA | 21745 |
rs387632010 | in-del | -/GACA | | | intron-variant | Tep1 | Mm_Celera | 14:50839854 | AGGTGGAGAGCAACA[-/GACA]ATTAACAGCTCCTCT | 21745 |
rs387663025 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50832607 | CAACAACAAAAAAAA[-/A]CCCCAGCATGCTCTA | 21745 |
rs387669792 | in-del | -/GGAACAA | | | intron-variant | Tep1 | Mm_Celera | 14:50863109 | TAGGAACAAGAACAA[-/GGAACAA]TTTCCTACTCCCATG | 21745 |
rs387680942 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50842114 | AGGAATGAAGAGGTT[-/A]AAAAAAAAAACAAAA | 21745 |
rs387791401 | in-del | -/CTTT | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871230 | ATTGTTTCTTTCTTT[-/CTTT]TTCAGACAGGGTCTC | 21745 |
rs387798319 | in-del | -/TATATATCTCA | | | intron-variant | Tep1 | Mm_Celera | 14:50825247 | AGGATATATATGACA[-/TATATATCTCA]CAAAATATTAGTATT | 21745 |
rs387816541 | in-del | -/TCGC | | | intron-variant | Tep1 | Mm_Celera | 14:50826722 | CTGCCTTTCCCTCGC[-/TCGC]CTTACACTCCATGGT | 21745 |
rs387820548 | in-del | -/AA | | | intron-variant | Tep1 | Mm_Celera | 14:50849857 | ATTTAAAAAAAAAAA[-/AA]GGCAGTGAAGGTTGG | 21745 |
rs387832205 | in-del | -/GAGAGAGACAGA | | | intron-variant | Tep1 | Mm_Celera | 14:50856914 | AGAGAGAGAGAGAGA[-/GAGAGAGACAGA]CCAGACAGACAGACA | 21745 |
rs387865045 | in-del | -/AAAA | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869370 | AAAAAAAAAAAAAAA[-/AAAA]GGTGGGAAGCTAGAA | 21745 |
rs387880931 | in-del | -/ACACTGGAGA | | | intron-variant | Tep1 | Mm_Celera | 14:50839560 | GGAGAACACTGGAGA[-/ACACTGGAGA]CAGGAGACAGACTGG | 21745 |
rs387885706 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50861449 | AAGGAAGAAAGGAAG[A/G]AAGGAAGGAAGGAAG | 21745 |
rs387891031 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50867959 | ATATAGCAAAAAAAA[-/A]GGCTAGAGTCAAGAT | 21745 |
rs578351833 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50827825 | CCAGCCTGGTCTACA[A/G]AGTGAGTTCCAGGAC | 21745 |
rs578369908 | snp | C/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50855725 | GGGGGACAGGATAAA[C/G]CAAGTGAGTGACACA | 21745 |
rs578370744 | snp | A/C | | | intron-variant | Tep1 | GRCm38.p3 | 14:50865008 | ATCAGCTCCTGCTTC[A/C]TGACCTGCTTAGTTC | 21745 |
rs578585411 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839923 | ACACACACACACATA[C/T]GACATACACATACAC | 21745 |
rs578612445 | snp | A/C | | | intron-variant | Tep1 | GRCm38.p3 | 14:50859080 | TACAATATATAACAA[A/C]CAACAAAGGCATTTG | 21745 |
rs578714993 | snp | A/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50853407 | ATAATCAAGGCTGAC[A/T]AAAACTGTCCCAGGG | 21745 |
rs578829596 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | GRCm38.p3 | 14:50868718 | GTTATTATTATTATC[A/G]TGTGTGTGTGTGTGT | 21745 |
rs578856216 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50832458 | ACAGATCCCATTACA[A/G]ATGGTTGTGAGCCAC | 21745 |
rs578921480 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839699 | AGACAGGGTTTCTCT[A/G]TGTAGCCCTGGCTGT | 21745 |
rs578937274 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50860423 | CAAACTTCAAAAATC[C/T]AGTTTTTTGGTTATG | 21745 |
rs579193836 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50829839 | GTACACCTTCTCTAT[C/T]GCTCCCCACTCCAGT | 21745 |
rs579203042 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50866894 | TGGCTGTTATAAAAT[C/T]GCACCACGAATGCAT | 21745 |
rs579287640 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50856228 | CACTCTCTTAGTAAA[C/T]GGAGAGCCTTGAACA | 21745 |
rs579306152 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839437 | TCTACAGAGTGAGTT[C/T]CAGGACAGCCAGGGA | 21745 |
rs579383326 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50859423 | ACTCCAATGAGGCCA[C/T]ACCCACTCCAACAAG | 21745 |
rs579514098 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50835084 | CGCTTGGGAGGCAGA[A/G]GCAGGTGGATTTTTG | 21745 |
rs579592597 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50857641 | ATAAATCTTTAAAAA[A/G]AAAAAGAAACAAAAA | 21745 |
rs579719571 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50848514 | CTCTCTCTCTCTCTC[C/T]CTCTCCCTCTCCCTC | 21745 |
rs580000666 | snp | A/C | | | intron-variant | Tep1 | GRCm38.p3 | 14:50857632 | AATAAATAAATAAAT[A/C]TTTAAAAAAAAAAAG | 21745 |
rs580149676 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50846298 | TTAACTTTCAACCCT[C/T]TGAGAACGCAGGGAA | 21745 |
rs580300079 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50856359 | TACAACAGTTCAACT[A/G]GTACAATATACTCTT | 21745 |
rs580410878 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50836504 | TACTTCTCTGCCCCG[C/T]CCCTGCCCCCGCCCC | 21745 |
rs580502589 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50861822 | GGGGCTGGAGAGACT[A/G]CTCAATTGTAAAAAA | 21745 |
rs580647031 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50825961 | AAAAAAAAATCACAA[C/T]TAGGAAACCTAGGAG | 21745 |
rs580670429 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50842533 | TGTGTGTGTGTGTGT[A/G]TGTTGAACACTCACA | 21745 |
rs580807638 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839408 | GTAAATTTCTGAGTT[C/T]GAGGCCAGCCTGGTC | 21745 |
rs580812272 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50827805 | GTGGATTTCTGAGTT[C/T]GAGGCCAGCCTGGTC | 21745 |
rs580992807 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50864790 | GATACAAGCTGGAGT[C/T]ATCACAGAGAAAGGA | 21745 |
rs581138440 | snp | C/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50838756 | CAGTAGTTCTGGTCT[C/G]TTCTGCCTCTTTCTC | 21745 |
rs581217386 | snp | A/C | | | intron-variant | Tep1 | GRCm38.p3 | 14:50859030 | ACCGGTACAGAGAGA[A/C]TATTACATAGCAAAG | 21745 |
rs581458606 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50862382 | CGCCCAGCGCTGCTG[A/G]GATTTCTAAAACTGA | 21745 |
rs581467997 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50857748 | TGTTCTGGCCTTTCT[A/G]TGCACTCTGGGTGAC | 21745 |
rs581484134 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50826445 | GGAGAAGGAAGGAAG[A/G]AAGGAAGGAAGGAAG | 21745 |
rs581648788 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839496 | AAACAAACAAACAAA[C/T]AGCCAGGTGTGGCCA | 21745 |
rs581798671 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50859096 | CAACAAAGGCATTTG[A/G]GCTCAAAAATTCCAA | 21745 |
rs581807756 | snp | C/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50855726 | GGGGACAGGATAAAG[C/G]AAGTGAGTGACACAT | 21745 |
rs582028814 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50842479 | ACCAAGCATATACAA[A/G]TGTGTGTGTGTGTGT | 21745 |
rs582040478 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50833286 | AAAGATTAACTGTGG[C/T]GATAATGATTGAGCC | 21745 |
rs582174168 | snp | A/C | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | GRCm38.p3 | 14:50868770 | TGTGTGTGTGTATTG[A/C]GAGAGGGAGAGGGGA | 21745 |
rs582282870 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839761 | TCGAACTCAGAAATC[C/T]ACCTGTCTCTGCCCC | 21745 |
rs582283900 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50854629 | GGACGGTGAGCAGAG[A/G]AGGAAGAAGGATGAG | 21745 |
rs582477033 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50861277 | AAAGGCCCCGGCAGC[A/G]TCAGCAACTTGAGAG | 21745 |
rs582585009 | snp | A/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50832405 | TTTTATGTATATGAA[A/T]ACACTGTAGCTGTCT | 21745 |
rs582586968 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50866895 | GGCTGTTATAAAATT[A/G]CACCACGAATGCATG | 21745 |
rs582754911 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50859426 | CCAATGAGGCCACAC[C/T]CACTCCAACAAGGCC | 21745 |
rs582975404 | snp | A/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50857643 | AAATCTTTAAAAAAA[A/T]AAAGAAACAAAAAGG | 21745 |
rs583046499 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | GRCm38.p3 | 14:50872136 | GTGCTCTGCACAGTT[A/G]CTAAGGGTCTAGCAC | 21745 |
rs583069757 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50835097 | GAGGCAGGTGGATTT[C/T]TGAGTTCGAGGCCAG | 21745 |
rs583128881 | snp | C/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50838878 | CAGTAGTTCTGGTCT[C/G]TTCTGCCTCTTTCTC | 21745 |
rs583297951 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50848620 | CCCTCTTTCCCCCCC[C/T]CTCTCTCCAGGGTCT | 21745 |
rs583412377 | snp | A/C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50857636 | AATAAATAAATCTTT[A/C/T]AAAAAAAAAAGAAAC | 21745 |
rs583559807 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50848484 | ATAATTTTTTCATAT[C/T]GCTCCTCTCTCTCGC | 21745 |
rs583607484 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50862387 | AGCGCTGCTGAGATT[C/T]CTAAAACTGATGGAG | 21745 |
rs583644302 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50827752 | CCTGGGCGTGGTGGC[A/G]CATGCCTTTAATCCC | 21745 |
rs583685199 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50837977 | GAAGAAAAAGCTGTG[A/G]CTCTCTCCAGTCTGG | 21745 |
rs583988134 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50825964 | AAAAAATCACAACTA[A/G]GAAACCTAGGAGACA | 21745 |
rs583990381 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50862200 | TACCACACTGGCTGC[C/T]GGGATTTTTTTTTTT | 21745 |
rs584100079 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50859420 | CCCACTCCAATGAGG[C/T]CACACCCACTCCAAC | 21745 |
rs584151191 | snp | C/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50864947 | GAGCAGGCTGAGCAA[C/G]CCAAGGGAAGCAAGC | 21745 |
rs584223528 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839422 | TCGAGGCCAGCCTGG[C/T]CTACAGAGTGAGTTC | 21745 |
rs584390093 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50827810 | TTTCTGAGTTCGAGG[C/T]CAGCCTGGTCTACAG | 21745 |
rs584462663 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50854638 | GCAGAGGAGGAAGAA[A/G]GATGAGGAGCCATGG | 21745 |
rs584698259 | snp | A/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50859034 | GTACAGAGAGACTAT[A/T]ACATAGCAAAGCAAT | 21745 |
rs584716117 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50853404 | TCCATAATCAAGGCT[A/G]ACTAAAACTGTCCCA | 21745 |
rs584820687 | snp | G/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50852755 | AGAGAGGCAGAAAGA[G/T]AGAGAGAGACAGAGA | 21745 |
rs584955297 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839686 | GTTTTTTTTTCCGAG[A/G]CAGGGTTTCTCTGTG | 21745 |
rs585063833 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50857978 | AAAGAAACTCTATCT[C/T]GAAAATAAAAGGGGG | 21745 |
rs585081871 | snp | A/C | | | intron-variant | Tep1 | GRCm38.p3 | 14:50849831 | AAAAAAAAAGAAAAC[A/C]AAAGTGCTCTATTTA | 21745 |
rs585305440 | snp | A/C | | | intron-variant | Tep1 | GRCm38.p3 | 14:50829502 | ATAAATAAATACATA[A/C]ATAAATAAATAAATA | 21745 |
rs585311490 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50865111 | GCTTCTTGGTCATGA[C/T]GTTTGTGCAGGAATA | 21745 |
rs585380922 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50842531 | TGTGTGTGTGTGTGT[A/G]TGTGTTGAACACTCA | 21745 |
rs585439643 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50861821 | AGGGGCTGGAGAGAC[C/T]ACTCAATTGTAAAAA | 21745 |
rs585479359 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839775 | CCACCTGTCTCTGCC[C/T]CCCAAGTGCTGGGAT | 21745 |
rs585545461 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50833829 | ATCAAAAAGTTCAAG[A/G]AAGCAATGGGAAATA | 21745 |
rs586023559 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50866898 | TGTTATAAAATTGCA[C/T]CACGAATGCATGCAC | 21745 |
rs586112475 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50845292 | TGAAACTTTGTACTA[A/G]AGTCGGAGTGGAAAA | 21745 |
rs586146696 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50857431 | AAGTAAAAAATATTT[C/T]TAAAGATTAAGAAAC | 21745 |
rs586255601 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50859436 | CACACCCACTCCAAC[A/G]AGGCCACACCCACTC | 21745 |
rs586389201 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | GRCm38.p3 | 14:50872226 | ATGTGTGTGTGGGGG[A/G]GAGAGAGAGAGAGAG | 21745 |
rs586413607 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50835293 | GAGACAGAGAGAGAG[A/G]CAGAGAGAGAGACAG | 21745 |
rs586549459 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50863096 | ATCCTAGAGTTACAT[A/G]GGAACAAGAACAATT | 21745 |
rs586728421 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50849414 | GGTTACTGGGTACTG[A/G]GTACTGAGTACTGGG | 21745 |
rs586842781 | snp | A/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50857637 | ATAAATAAATCTTTA[A/T]AAAAAAAAAGAAACA | 21745 |
rs586848090 | snp | A/C | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839354 | AGCCGGGCGTGGTGG[A/C]GCACACCTTTAATTT | 21745 |
rs586979255 | snp | A/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50827804 | GGTGGATTTCTGAGT[A/T]CGAGGCCAGCCTGGT | 21745 |
rs587081469 | snp | A/G/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50848498 | TCGCTCCTCTCTCTC[A/G/T]CTCTCTCTCTCTCTC | 21745 |
rs587138622 | snp | A/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50857644 | AATCTTTAAAAAAAA[A/T]AAGAAACAAAAAGGG | 21745 |
rs587195286 | snp | A/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50858383 | CCCCCTGCCTCCCCC[A/T]CTGCCCCCCTCCCCC | 21745 |
rs587282840 | snp | A/C | | | intron-variant | Tep1 | GRCm38.p3 | 14:50825969 | ATCACAACTAGGAAA[A/C]CTAGGAGACAGGCAT | 21745 |
rs587285688 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50862380 | CACGCCCAGCGCTGC[C/T]GAGATTTCTAAAACT | 21745 |
rs587403806 | snp | C/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50852775 | AGAGACAGAGAGACA[C/G]AGAGACAGAGAGAGA | 21745 |
rs864256824 | snp | A/C/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50852803 | AGACAGAGCGAGAAC[A/C/G]AGAACACTTTGTATC | 21745 |
rs864271111 | snp | C/T | | | utr-variant-3-prime | Tep1 | GRCm38.p3 | 14:50824065 | GGCATACACTCTAGA[C/T]CTCTCAACATTTTAG | 21745 |