SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4173870 | snp | A/G | 0.497654 | 0.0341661 | missense | Hcls1 | GRCm38.p3 | 16:36946692 | ATGGCTATGGCGGTC[A/G]GTTTGGAGTGGAGAG | 15163 |
rs4173871 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hcls1 | Mm_Celera | 16:36948149 | ACATTGGAAAGTTCA[A/G]AATTCACTTCTACAC | 15163 |
rs4173872 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hcls1 | GRCm38.p3 | 16:36953744 | GTGTGTGTGTGTGTG[C/T]GCGCATGCGCATGCG | 15163 |
rs4173873 | snp | A/G | 0.5 | 0 | intron-variant | Hcls1 | GRCm38.p3 | 16:36954329 | GCGCTAGAATCCCAG[A/G]CACACACTAGCACAC | 15163 |
rs6153976 | snp | A/G | 0.5 | 0 | intron-variant | Hcls1 | Mm_Celera | 16:36956071 | TACGGTAAAGTGGGT[A/G]CAAGGGAAGAGAGAA | 15163 |
rs6154576 | snp | G/T | 0.5 | 0 | intron-variant | Hcls1 | Mm_Celera | 16:36956185 | CTCTGAGGTTTAAGT[G/T]AGAANAGTGTAGGGT | 15163 |
rs6154578 | snp | C/G | 0.5 | 0 | intron-variant | Hcls1 | Mm_Celera | 16:36956190 | AGGTTTAAGTNAGAA[C/G]AGTGTAGGGTGGCTG | 15163 |
rs6155101 | snp | A/G | 0.5 | 0 | intron-variant | Hcls1 | Mm_Celera | 16:36956264 | GCTTTTCTTAATCCT[A/G]TCTTGAGTCTCTCCT | 15163 |
rs6156304 | snp | A/G | 0.5 | 0 | intron-variant | Hcls1 | Mm_Celera | 16:36956520 | CAGGTACTGTCTTAT[A/G]GATCACTACTCCCTT | 15163 |
rs6312645 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Hcls1 | Mm_Celera | 16:36944440 | GAATTTTGCTAGATT[C/T]GCTTGCTCCNTCAAT | 15163 |
rs6312667 | snp | A/G | 0.5 | 0 | intron-variant | Hcls1 | Mm_Celera | 16:36944450 | AGATTNGCTTGCTCC[A/G]TCAATACAAGCCATG | 15163 |
rs6312772 | snp | C/T | 0.5 | 0 | intron-variant | Hcls1 | Mm_Celera | 16:36944504 | TGTGTCAAAAGTCTC[C/T]TAGGTATGACACTTG | 15163 |
rs6327324 | snp | C/T | 0.5 | 0 | intron-variant | Hcls1 | Mm_Celera | 16:36951465 | AGTTTAAATTTAAAG[C/T]TAATCATGTCTTTGT | 15163 |
rs6328352 | snp | A/G | 0.5 | 0 | intron-variant | Hcls1 | Mm_Celera | 16:36951643 | gagggagaggcaggt[A/G]aatcaaggccagcct | 15163 |
rs6328959 | snp | C/T | 0.5 | 0 | intron-variant | Hcls1 | GRCm38.p3 | 16:36951747 | GCAAAGCcatacaca[C/T]acacacacacacaca | 15163 |
rs6329055 | snp | C/T | 0.5 | 0 | intron-variant | Hcls1 | Mm_Celera | 16:36951795 | acacacacacacaca[C/T]anacatatatatata | 15163 |
rs6329058 | snp | C/T | 0.5 | 0 | intron-variant | Hcls1 | Mm_Celera | 16:36951797 | acacacacacacana[C/T]acatatatatataga | 15163 |
rs31747075 | snp | C/G | 0.32 | 0.24 | intron-variant | Hcls1 | Mm_Celera | 16:36959669 | AGATCCTGGGTAGAT[C/G]TCATACAGACCTTAA | 15163 |
rs32286714 | snp | A/G | 0.32 | 0.24 | intron-variant | Hcls1 | GRCm38.p3 | 16:36959569 | AGATATTCCATGACA[A/G]AAACCAAATTTACAC | 15163 |
rs32420463 | snp | A/T | 0.32 | 0.24 | intron-variant | Hcls1 | Mm_Celera | 16:36959674 | CTAGAAGATCCTGGG[A/T]AGATCTCATACAGAC | 15163 |
rs45641614 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36941119 | GCTGGGAATGGGCTA[A/G]GTGACCTTGGACAAA | 15163 |
rs45749448 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, downstream-variant-500B | Hcls1, Fbxo40 | Mm_Celera | 16:36963199 | AAAACTGAAAATAAA[A/G]TGAGACTGTGGCTAA | 15163 |
rs45895858 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36954150 | CTTTCTCTGTGTATG[A/C]ATGCACAAGCATGTA | 15163 |
rs45897242 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hcls1 | Mm_Celera | 16:36949160 | AAAGGAAAAGACAGT[A/G]CTAAGCAAGTACAGG | 15163 |
rs45959380 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36957017 | TTCGTCACATGGAAT[A/C]TGGGCTTCAGTGCCC | 15163 |
rs46116852 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Hcls1 | Mm_Celera | 16:36949126 | CTAGAGGCTCCTGCA[A/T]ACACAAGGGTAGTTT | 15163 |
rs46153936 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36936322 | AGGCTTCCAGATGGG[G/T]ATAGAAAGTGGAGAC | 15163 |
rs46273220 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hcls1 | Mm_Celera | 16:36945479 | ATAACGCTATGCGGT[C/T]CCAGGAGTCCTTGCA | 15163 |
rs46287129 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36958969 | TTACTAAAGCTTAAA[A/G]CACACATTGTAACCC | 15163 |
rs46320560 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36942128 | TCGCCGTGAAGAGCC[G/T]CGGCTATGCCATGAG | 15163 |
rs46401267 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36948812 | GTCAGGTCTCATGAC[G/T]TCTCTTGCTGGTGCT | 15163 |
rs46435835 | snp | C/G/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | GRCm38.p3 | 16:36939868 | TCAAGGCAAATACAG[C/G/T]GAATGACATAATATG | 15163 |
rs46436940 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36958923 | TCCATTGCTGAGAGT[G/T]GGGTGTTGAAGTCTC | 15163 |
rs46548770 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36948033 | TTTTTTTTTTGTGGG[G/T]GCTAAAGATTTGATC | 15163 |
rs46564134 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36941840 | AGCAGGTCAGCTCCC[A/T]GACTGTGCTGTGAGC | 15163 |
rs46743666 | snp | C/T | 0.231111 | 0.249285 | utr-variant-5-prime | Hcls1 | Mm_Celera | 16:36935054 | GTAGATGTGAAAAGC[C/T]GTAACCAGGAACCAG | 15163 |
rs46751725 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36958925 | CATTGCTGAGAGTGG[A/G]GTGTTGAAGTCTCCC | 15163 |
rs46762034 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36948108 | CCCTCTTCAGCCCCT[C/T]GGCCATTTAGTGATC | 15163 |
rs46955880 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hcls1 | Mm_Celera | 16:36948758 | CCATGCTTCTCAGGT[A/G]ACAGACAGGACAGCA | 15163 |
rs47034707 | snp | A/C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36958879 | TGCAAACTAAACAGA[A/C/G]ACAAATTGAAATTAA | 15163 |
rs47082306 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Hcls1, Fbxo40 | Mm_Celera | 16:36963152 | TTTCTTCCCTTAGCA[A/G]ACAAATTGGAACTGC | 15163 |
rs47140827 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36935289 | AGCATGATTGAGCAC[A/C]TATCTAGGACCCTGG | 15163 |
rs47161735 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36954396 | TGGGACCCAAACCCA[G/T]GTCCTCATAGTTGCA | 15163 |
rs47195130 | snp | A/T | 0.231111 | 0.249285 | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934389 | AGGCCAGTAGTCAGA[A/T]CTCTGTAAGTGAGCT | 15163 |
rs47365200 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hcls1 | Mm_Celera | 16:36961425 | GTGTAGCAATGTCTC[A/C]TTCTTCAGGTCTGGC | 15163 |
rs47376730 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36954239 | AACTTAACTCTTGAG[A/G]CTGGGTCTCTCTTAA | 15163 |
rs47393143 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36958874 | TTCTATTAGTTTCAA[C/T]GTGTCTCTGTTCAGT | 15163 |
rs47419669 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Hcls1 | Mm_Celera | 16:36946820 | TATCCTAAATATGGT[A/T]TGCATGGTGTCCATT | 15163 |
rs47551854 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36938285 | ATCTAAACTTTTACA[A/G]AAGTGTAGAACATGT | 15163 |
rs47585421 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36953990 | ACTAGATTTGATGCC[A/G]GTGTATTTATTCCTG | 15163 |
rs47653640 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36958931 | AATAGTGGGAGACTT[C/T]AACACCCCACTCTCA | 15163 |
rs47997944 | snp | C/G | | | missense | Hcls1 | Mm_Celera | 16:36962174 | CAGGATGAGGATGCA[C/G]AGGGAGACTATGAGG | 15163 |
rs48035154 | snp | A/G | 0.231111 | 0.249285 | utr-variant-5-prime | Hcls1 | Mm_Celera | 16:36935068 | CCGTAACCAGGAACC[A/G]GTAAAGGTGGGTGCT | 15163 |
rs48059108 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36937415 | GTGAAGTGGTCAGGA[A/G]CACCTCAGCCACTCT | 15163 |
rs48143901 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36953893 | ATTCTTTTTGTTCCA[C/T]GGGTTTAATTTTCCA | 15163 |
rs48203082 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36958933 | GTAATAGTGGGAAAC[A/T]TCAATACCCCACTCT | 15163 |
rs48231875 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36937062 | CAAGCTGTGGACATA[A/G]TGAACAATCCCAACA | 15163 |
rs48358405 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36948190 | CAGGAAAGATCCAGC[A/T]CAAAGATACCTGGTT | 15163 |
rs48398361 | snp | G/T | 0.231111 | 0.249285 | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934682 | GTACCCCTAAGTGCT[G/T]GGATCACAGAAGTTC | 15163 |
rs48516663 | snp | G/T | 0.124444 | 0.216185 | synonymous-codon | Hcls1 | Mm_Celera | 16:36962197 | CTATGAGGATGTGCT[G/T]GAGCCCGAGGACACC | 15163 |
rs48528022 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36940518 | GTGTTCTGGGAAGTG[C/T]TGACCTGAGAGAGCA | 15163 |
rs48585804 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36935218 | CTAAGGACTGTGTGC[A/C]GTGGTTGACAATGAA | 15163 |
rs49071180 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36948868 | CAAATCATCAATTTA[C/T]GTTCAGCAGGGCTCA | 15163 |
rs49285393 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36954099 | TTCATGTTGTATTCA[A/T]GTTACCTTTCATAGG | 15163 |
rs49286794 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36941107 | AGCTGGGACCCTGCT[A/G]GGAATGGGCTAAGTG | 15163 |
rs49368355 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36957039 | TCAGTGCCCTAGGAT[C/T]CCCAGGCCTTATGGC | 15163 |
rs49390375 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36953919 | TTCCAACACTGGCTG[A/C]ATCTATTTGTCTTAC | 15163 |
rs49419264 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36942284 | AGGCTATAGACATAA[A/T]ATAGACAGATAATAA | 15163 |
rs49436459 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36935272 | ATGGCCTGCACTCGG[A/G]GAGCATGATTGAGCA | 15163 |
rs49456279 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB, downstream-variant-500B | Hcls1, Golgb1 | Mm_Celera | 16:36933556 | TTTCATAGCTCATGC[A/G]GGTTGGGTAGACATC | 15163 |
rs49468677 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36937802 | ACAGAGCACATTTCT[C/T]GCTGACACTGTTGCC | 15163 |
rs49502208 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934566 | CATACAGATCATTTT[C/T]CCACTAAGCCTTTTT | 15163 |
rs49529878 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36958924 | GGAAACTTCAATACC[C/T]CACTCTCATCAATGG | 15163 |
rs49598531 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36954100 | TCATGTTGTATTCAT[G/T]TTACCTTTCATAGGC | 15163 |
rs49648682 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36933729 | TGTGAGGGGGAAGTG[A/G]GTTTCCTTGGTGTCA | 15163 |
rs49969807 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36940776 | TGGATTGAATAGTAT[A/G]TGTGACTGACTGTCT | 15163 |
rs49996560 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hcls1 | Mm_Celera | 16:36949062 | TGATTAGGGCTGCAA[C/T]ACTTCGAGAAGGTGA | 15163 |
rs49998521 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36935183 | GGTCTTTACTAATAG[A/G]TGCTGAACTCTTGAT | 15163 |
rs50020455 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36940087 | TGGAATGTCTCTGAA[C/T]ACGGTAGAGACCTAA | 15163 |
rs50046007 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36954316 | CTCTGCCTCTCCAGC[A/G]CTAGAATCCCAGGCA | 15163 |
rs50055454 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36940365 | AGTGTTACTCTTAAA[C/T]GAATCAAGCAATACT | 15163 |
rs50096076 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Hcls1 | Mm_Celera | 16:36962062 | GGAAGAGCCAGTGTA[C/T]GAAGCAGCACCCGAG | 15163 |
rs50115119 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, downstream-variant-500B | Hcls1, Golgb1 | Mm_Celera | 16:36933191 | TCTGAGACTCCTTCA[C/T]CTCACTGGCCAGCAC | 15163 |
rs50158024 | snp | A/C/G | 0.231111 | 0.249285 | intron-variant | Hcls1 | GRCm38.p3 | 16:36937035 | GTGTTGTATGACCAC[A/C/G]GGTCACCCCTACAAG | 15163 |
rs50241626 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hcls1 | Mm_Celera | 16:36946466 | TGCTTATACCAACCT[C/T]TTACTCTAAGCCTGT | 15163 |
rs50255460 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36948169 | CACTTCTACACTTAT[C/T]CAGGCCAGGAAAGAT | 15163 |
rs50601691 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36935384 | CCTGAAGGCGACCCA[C/T]GGAAGATGAGGACAA | 15163 |
rs50603736 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hcls1 | Mm_Celera | 16:36939795 | CCATAGGCTAGTCAG[A/G]ATCATCTAACCAGGA | 15163 |
rs50606442 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36948221 | GATGGAGGAAAAACA[G/T]CAGTTGCTTGCGGTA | 15163 |
rs50642300 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36954196 | AGGAGCCAAAGGTCA[A/G]TGTTGGGTGTATTCT | 15163 |
rs50786053 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36936809 | TGTGAGTAGTTCAAC[C/T]AGTCTGTCCCACTGG | 15163 |
rs50814034 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Hcls1 | Mm_Celera | 16:36962901 | TTAAGAGCTTTAGGT[A/G]GAATCGCTCCAGGTG | 15163 |
rs50815245 | snp | A/C | 0.231111 | 0.249285 | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934357 | GTATGTCAGAGTTCA[A/C]TTCACCAGCTTAGAG | 15163 |
rs50883497 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36933852 | CTATAAATAGCCTTA[C/T]TAGAACAAATAAAGT | 15163 |
rs50949782 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36953906 | CACGGGTTTAATTTT[C/T]CAACACTGGCTGCAT | 15163 |
rs51089765 | snp | A/C | 0.231111 | 0.249285 | missense | Hcls1 | Mm_Celera | 16:36957253 | GCAAAATTTGAGTCC[A/C]TGGCTGAGGAGAAGA | 15163 |
rs51119517 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36941039 | GTAAATGTTGGAGAT[A/G]GTTTCACAAAAGCTT | 15163 |
rs51131993 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36936753 | TAGTTGAACATTTAC[A/G]TAATAAAAATAAAGC | 15163 |
rs51321604 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hcls1 | Mm_Celera | 16:36949113 | AGCTGGAGTGTTGCT[A/G]GAGGCTCCTGCAAAC | 15163 |
rs51359997 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hcls1 | Mm_Celera | 16:36941978 | TTTACACAAAGTGCA[A/C]ATAAAGAACTGCAGA | 15163 |
rs51401942 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36954454 | CAGCACCTGCCATGT[A/G]TGTATTTTCTGAGAT | 15163 |
rs51462395 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36948029 | TTTTTTTTTTTTTTG[G/T]GGGTGCTAAAGATTT | 15163 |
rs51484955 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36954355 | CACACTATCACACTA[G/T]CACATGTAGTTTTGT | 15163 |
rs51489823 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934768 | AGGACACAGAGCAGT[C/T]CTGCAGCATTCTTAT | 15163 |
rs51517990 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Hcls1 | Mm_Celera | 16:36937844 | GTAGAATGACATCTC[C/T]GAGAAGGAGCAACGG | 15163 |
rs51555518 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36936057 | AGTTTCCTTCTGTGG[C/T]AGAGTAGCCTGAGAG | 15163 |
rs51557219 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B | Hcls1, Fbxo40 | Mm_Celera | 16:36963179 | CTGCCCTTCTGTTTA[A/G]TCCTAAAACTGAAAA | 15163 |
rs51562021 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36954277 | GATCACATATTTGAC[A/C]ACACCAGCACTCAGG | 15163 |
rs51660068 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Hcls1 | Mm_Celera | 16:36949038 | AAATAAGCGAATACG[A/C]CAGCCAATTGATTAG | 15163 |
rs51755527 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36942378 | AATAAACATAATTTG[C/T]CATGTCCACAATTCT | 15163 |
rs51768435 | snp | A/T | 0.231111 | 0.249285 | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36933628 | GTATCACAGGGTAGA[A/T]GAGGATTAATGGGAA | 15163 |
rs51799159 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36954339 | CCCAGGCACACACTA[G/T]CACACTATCACACTA | 15163 |
rs51811245 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36935745 | GGGGTCTCACAGGGG[C/T]TGTCATATTACTGCA | 15163 |
rs51917172 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934782 | TCCTGCAGCATTCTT[A/G]TTGTGTCTTAACTGA | 15163 |
rs51936940 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36953996 | TTTGATGCCGGTGTA[C/T]TTATTCCTGGTGGAC | 15163 |
rs52032562 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hcls1 | Mm_Celera | 16:36936184 | CAGATGTTCTTAATA[G/T]CTCACAGTGACTCTG | 15163 |
rs52219628 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hcls1 | Mm_Celera | 16:36949264 | ATCCTTTTTCATGGT[A/G]CAGATTGGAGTCTCA | 15163 |
rs52411926 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Hcls1 | Mm_Celera | 16:36949499 | GGGAAGTGCTAGGAT[G/T]GTAATTATTTGGAGA | 15163 |
rs52698907 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36951811 | ATACATATATATATA[G/T]AGAGAGATTATATAT | 15163 |
rs52698909 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36951813 | ACATATATATATAGA[G/T]AGAGATTATATATAA | 15163 |
rs211915569 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36947734 | ATGCATGGTATATGC[A/G]TATGTTGTATATGGT | 15163 |
rs211919946 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36936133 | TCTTTATGTGTCTTA[C/G]CCCCTGTTAGTAGCT | 15163 |
rs212059073 | in-del | -/TCA | | | intron-variant | Hcls1 | Mm_Celera | 16:36950246 | CAGTAGCCTACAGAG[-/TCA]TGGAAACTGGGAAGA | 15163 |
rs212125921 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36940632 | CTGCTGTGAGCCGGT[A/G]GGAAGAGCTTGCGTT | 15163 |
rs212187099 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36941543 | TCTCTGTGTTTGTCT[A/C]TGCCTGGAAGAGGAA | 15163 |
rs212301414 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36956865 | TCAGAGACACGCAGG[A/G]AAGAGAGAGGAAATG | 15163 |
rs212343730 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36951105 | AAGCAGAGAGCCTGG[A/C]TAATCATTTATCTTT | 15163 |
rs212408501 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36939968 | TCCCAACTCCTCCTT[A/C]CACACATGACAATAT | 15163 |
rs212555598 | in-del | -/AA | | | intron-variant | Hcls1 | Mm_Celera | 16:36956836 | GAGGTGGCATTAGGG[-/AA]AAAAAACTGAGGATC | 15163 |
rs212571769 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36952755 | CCTGTCTCCATGTGG[A/G]TGCCCCCACCTCCCA | 15163 |
rs212589243 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Hcls1, Golgb1 | Mm_Celera | 16:36933584 | ATCATGCTCTTATAC[A/G]AAGTTGCCACTTGGG | 15163 |
rs212589998 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36955925 | AATTCCCAGCCTTCT[A/C]ATCTCCTGTTTTCAC | 15163 |
rs212616182 | snp | A/G | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934394 | AGTAGTCAGAACTCT[A/G]TAAGTGAGCTCAGAC | 15163 |
rs212698907 | snp | C/T | | | synonymous-codon | Hcls1 | Mm_Celera | 16:36961533 | ACGAGGCAGTCTCCA[C/T]TGCAGAATCACTTGG | 15163 |
rs212815683 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36943678 | TGAGTTAAGGCTCTT[C/T]TTCTCTATGGATATC | 15163 |
rs212901167 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36953209 | TTTGAAAGTGTGTGT[A/G]TGTGTGTGTGTATAT | 15163 |
rs213113442 | snp | C/T | | | synonymous-codon | Hcls1 | Mm_Celera | 16:36962719 | TGGCCACTTTGGACT[C/T]TTCCCTGCAAACTAT | 15163 |
rs213401609 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36935847 | TCATTGCCTGTCTCC[A/G]GCCTCCTACTTTAAG | 15163 |
rs213431389 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36946886 | GCCTTTTTTTCTCTC[C/T]GGATCTCAATACCCA | 15163 |
rs213516948 | in-del | -/ACCTTCCTCTCAATTCTCTTTTTC | | | intron-variant | Hcls1 | Mm_Celera | 16:36937229 | TTAGCATCCTTACCA[-/ACCTTCCTCTCAATTCTCTTTTTC]ACTCCTAATTATTTC | 15163 |
rs213617561 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36952543 | TGTGGGCTTCTCTTC[C/T]TCCTCCTCCTCCTTC | 15163 |
rs213630416 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36944543 | AAAGCTTCCCTGTAT[A/C]CCTTCCATCTGTCCA | 15163 |
rs213712984 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36955012 | TTTGTCCCAGAGATG[A/T]TCTCTCACGGGCTCT | 15163 |
rs213791584 | snp | A/G | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934982 | CCTGAAAACGGAACT[A/G]GAGCAGCTGCTCTGT | 15163 |
rs213959290 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36948728 | CTTGCCGCCACCCAG[C/T]CCTGAAGTGTTGGCC | 15163 |
rs214035889 | in-del | -/T | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934461 | CCTCCACGTTCTGCC[-/T]TCTCCCTTCCTCGTG | 15163 |
rs214091064 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36960698 | GTCAGCTCCACAGTG[A/C]AGTGGGAAACCAGAA | 15163 |
rs214142652 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36945523 | TGTGAACCTTTGTTG[A/T]CTGTCATTTGTTGGT | 15163 |
rs214278507 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36958754 | GTGACCAAATATATG[A/G]TCAGTTTTGGAAAAG | 15163 |
rs214287598 | in-del | -/CTAT | | | intron-variant | Hcls1 | Mm_Celera | 16:36938205 | TGAAGTTCTATAAGG[-/CTAT]CTGTCATATATCTAG | 15163 |
rs214305744 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36947792 | GGGTGGGTGCAGCTG[C/T]GTGTGCACAAGGAGA | 15163 |
rs214398656 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36950571 | TACTTAGAAACCCAT[A/T]GTTACCGAGCAAATG | 15163 |
rs214407253 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36958120 | CAGTTGTATTGAATA[C/T]AGGCTTTTGTACTAG | 15163 |
rs214425465 | in-del | -/A | | | intron-variant | Hcls1 | Mm_Celera | 16:36951711 | GAGAAACCCATTCTC[-/A]AAAAATCCAAATGAA | 15163 |
rs214468759 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36942890 | GGTCTTTTATTTCCC[A/G]TTACTGTCAAACAGT | 15163 |
rs214611289 | snp | A/G | | | utr-variant-3-prime | Hcls1 | Mm_Celera | 16:36962836 | TGCTGCAAGGACCTG[A/G]CTGAACATCATGAGA | 15163 |
rs214852469 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36951313 | CGGTTCCAATTGTGG[G/T]CAGGCTTCTTTCTCA | 15163 |
rs214926858 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36944384 | TGTCAGAACTGCTCC[A/G]CTTTATGCCTTTATT | 15163 |
rs215076077 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36960714 | AGTGGGAAACCAGAA[A/G]GATCCTATCCCGAGC | 15163 |
rs215182439 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36961228 | CACTAAGATTTATAG[A/T]CTCTACCTGTTTGAG | 15163 |
rs215184331 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36950575 | TAGAAACCCATAGTT[A/C]CCGAGCAAATGGGGA | 15163 |
rs215302746 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36943662 | ATGTGCGGCATGCAA[A/T]TGAGTTAAGGCTCTT | 15163 |
rs215421204 | in-del | -/CT | | | intron-variant | Hcls1 | Mm_Celera | 16:36954062 | TTGCCTTTTGGGATA[-/CT]CTCTCTCTCTTGAAG | 15163 |
rs215475474 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36943508 | ATGAAGTCTGATTTA[C/T]ATAAAAAGATTATTT | 15163 |
rs215736175 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36957004 | AGACTAGTGGTCCTT[C/G]GTCACATGGAATATG | 15163 |
rs215773135 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Hcls1, Fbxo40 | Mm_Celera | 16:36963013 | CTGCCTCCTTCAGCC[A/G]CACCCCAGCTCTGCC | 15163 |
rs215854687 | in-del | -/A | | | intron-variant | Hcls1 | Mm_Celera | 16:36943960 | AGTCAGCTTCTCGGG[-/A]AAAAAAAATGCCTCT | 15163 |
rs216177305 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36949482 | AGGACTGAGTCCAAG[A/T]TGGGAAGTGCTAGGA | 15163 |
rs216185367 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36949813 | ACCAGGCATGTGGTA[C/T]ATACTAACACCCAGG | 15163 |
rs216249269 | in-del | -/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36949422 | TGATGATGATGATGA[-/T]TGATGATGATGATGA | 15163 |
rs216303359 | in-del | -/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36946242 | TATTTAAAGTTATTT[-/G]GGGGGGCAGACTCTT | 15163 |
rs216355456 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36950468 | GCCTACAGAGAGAAT[C/G]TGAGGTCAGCCTTAG | 15163 |
rs216418256 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36949536 | AGCCAAAACAAAGTC[A/G]AGAAAATTCAAAATA | 15163 |
rs216491709 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36949913 | ACAGGATGAGAACAG[A/C]TGCAGCCAACCCCTC | 15163 |
rs216496162 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Hcls1, Golgb1 | Mm_Celera | 16:36933416 | CAGCACTGAGGAGGC[C/T]GAGGCAGGAGGACCA | 15163 |
rs216510140 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36939774 | TGAGAGATTCATACT[A/G]CTCGTCCATAGGCTA | 15163 |
rs216729878 | in-del | -/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36957549 | GCATTTCTTTTTTCC[-/T]TTTTTTATTAAACTA | 15163 |
rs216893483 | in-del | -/CGCGCATGCGCATGCGCGCGCGCGCGTCC | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36953744 | GTGTGTGTGTGTGTG[lengthTooLong]TATGCACATAGAGTC | 15163 |
rs216915167 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36941868 | AGCATTACATTGGAC[A/G]AGGCCTTTGGTGCGT | 15163 |
rs216925274 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36942705 | TGTGTCTGTAGTCAG[G/T]GCCCCTTGCTGAATA | 15163 |
rs216926809 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36950789 | CTCAGTGCAGGTACT[A/G]TAGATACCTTGTTTA | 15163 |
rs217067275 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36949602 | TTAAAGTCAATAATG[C/T]CATGTAGAGCTTGTA | 15163 |
rs217227324 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36946056 | AATACACAAATACTA[A/G]TAAATTTACCCCAAA | 15163 |
rs217240856 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36941716 | ACGAAGAAAATACAA[A/G]CACAATTTTTATCTT | 15163 |
rs217482558 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36948791 | GGCTATCAGTGCCTA[C/G]TAACGGTCAGGTCTC | 15163 |
rs217495083 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36939893 | AATATGGGTGAAAGT[C/T]GGAAAATCATGAATC | 15163 |
rs217500280 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36940696 | TCATTAGTGGTGTGA[A/T]CTCAGTCACAGCTAA | 15163 |
rs217502099 | in-del | -/A | | | intron-variant | Hcls1 | Mm_Celera | 16:36949131 | GGCTCCTGCAAACAC[-/A]AGGGTAGTTTTCGAA | 15163 |
rs217502195 | in-del | -/AAGC | | | intron-variant | Hcls1 | Mm_Celera | 16:36937636 | TGGGTGATTCAGAGT[-/AAGC]AAGGACATGTCTAGG | 15163 |
rs217558924 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36940378 | AACGAATCAAGCAAT[A/T]CTGGAAAGCATGTAG | 15163 |
rs217566875 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36957833 | AGAATATGTATTGTA[A/T]CTGTGGCTTTATAGA | 15163 |
rs217588082 | in-del | -/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36942429 | TCCCGTGATCAACTG[-/T]CCCCCTTTCCCTAGG | 15163 |
rs217704841 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36957060 | GCCTTATGGCTCTCT[C/G]ACTACCTCTGTGCCT | 15163 |
rs217796338 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36953020 | TTCCCTAATTCAACA[A/G]CAGGGGTCAGATGCT | 15163 |
rs217807087 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36947863 | TACCTTAGCCCCTTG[A/G]GACCGGCTTTCCCTC | 15163 |
rs217832854 | snp | A/G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36953421 | TTTCATGGAACAAAC[A/G/T]AACAAAACAAAACAA | 15163 |
rs217886604 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36951912 | TATTCTTCACATTTT[A/C]TCATTTCTTCCTGCT | 15163 |
rs218360842 | in-del | -/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36944007 | GGTCCACTGGAGTTG[-/T]TAGACCATTTAGAGG | 15163 |
rs218400613 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36939340 | AACCTCTCTGGTGGG[A/T]TTTAGGAAGTTGCTT | 15163 |
rs218727967 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36945033 | GGGGACCTCACACAG[C/T]CATTCAGAAGCTCCG | 15163 |
rs218732979 | snp | A/G | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934000 | AGCCAGGCAAGTCAG[A/G]GTCCACAGATGACTG | 15163 |
rs218736427 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36946185 | ATTAGTTGGTTTTCT[A/G]TTATCTGTAATATTT | 15163 |
rs218762051 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36943180 | TGTCAGCACTTGTTA[G/T]TGTTGGTATTTTGAA | 15163 |
rs218788169 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36935116 | TGAGGGGTTGGGAGC[A/G]CAGGGAAGTATGGAA | 15163 |
rs219031186 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36935955 | TGATGGGAGAGATGA[A/G]CTGAGACCTGGAGAA | 15163 |
rs219402455 | snp | A/G | | | intron-variant, utr-variant-3-prime | Hcls1, Fbxo40 | Mm_Celera | 16:36963471 | AAGCAGCTCGGAGAG[A/G]AAAGGGTTTATTTCA | 15163 |
rs219438140 | in-del | -/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36954721 | TCCCTATTCCTTACA[-/T]TTCGTCTTTAAAGCT | 15163 |
rs219457112 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Hcls1, Golgb1 | Mm_Celera | 16:36933116 | TGTTGGCACAGAAGT[C/T]ACATGCCTGTGTTTG | 15163 |
rs219458385 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36955071 | AATATTGCGATGCTC[A/G]TTTGGGATGGAAATG | 15163 |
rs219758858 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36952852 | TGAACACAGACCTGG[A/C]AGTCCTCAACTGTAT | 15163 |
rs219799462 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36955786 | CAACCCCCATACCCT[A/G]ACCCTTTTTATTTTC | 15163 |
rs219815804 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36953403 | AACTTCATGTTCTTT[C/T]TCTTTCATGGAACAA | 15163 |
rs220000978 | in-del | -/A | | | intron-variant | Hcls1 | Mm_Celera | 16:36936479 | GAGCCAGGAAGTCCC[-/A]AAAAGCTACCAGACC | 15163 |
rs220042008 | in-del | -/CTAT | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934730 | TTCTGAATTCTTTTA[-/CTAT]CTTAGATGCAACTGT | 15163 |
rs220049657 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36960852 | TGGGAGATCAGTTAT[C/T]TCTGGGAGGAATTTG | 15163 |
rs220116266 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36961903 | CAAGGAAAGGCTTTT[A/G]AATGGAAGGGAAGGG | 15163 |
rs220139609 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36955136 | CCCGAGCCCAGAGCC[C/T]TTCCCTGGCCTATCA | 15163 |
rs220187569 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36957120 | TCTCCTCCTGTATAT[C/T]TAACAGATCTCGCTC | 15163 |
rs220484375 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36947150 | CTCTAGGCCTGTGTT[A/G]TATAAATGTAGGGAC | 15163 |
rs220571368 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36949717 | GCACAAATTACATCG[A/C]CTCAGCAACCCATGT | 15163 |
rs220698255 | in-del | -/GATAGATAGATA | | | intron-variant | Hcls1 | Mm_Celera | 16:36957497 | CAAGTGATAGGCATG[-/GATAGATAGATA]GATAGATAGATAGAT | 15163 |
rs220783093 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36947870 | GCCCCTTGGGACCGG[A/C]TTTCCCTCTGAGTGT | 15163 |
rs220839506 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36952721 | CTGCTCCATATCCCA[C/T]ACCTCCTCCCCTCCC | 15163 |
rs220840920 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36944075 | TATGAACCCGTGGCA[C/T]TCCTCTACTTATTTA | 15163 |
rs220867029 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36958340 | ACTTGGTTGATTTCA[A/G]CCTTGCGTTTGATTA | 15163 |
rs220925483 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36950060 | TAGACGTGTTAACAG[A/G]CTGTGGAGCAAAGCT | 15163 |
rs220942545 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36944734 | TCAGTTGGGTGTGGC[C/T]ACAGATACCTATAAG | 15163 |
rs221132335 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36955418 | GTCGCACAGGGCCCG[A/C]ATTCCTTCTGTTTTG | 15163 |
rs221190887 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36956146 | TGTGCTGGGCTTCAA[C/T]ATCTAAGGAGTATGA | 15163 |
rs221296268 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36948921 | AGCATAGGAGAGGCC[A/C]GGGTTCATCAGCACA | 15163 |
rs221317345 | in-del | -/TATTTTT | | | intron-variant | Hcls1 | Mm_Celera | 16:36959396 | GCCAGCCCATCCTGG[-/TATTTTT]TATTTTTTATTTTTA | 15163 |
rs221446548 | snp | C/T | | | downstream-variant-500B | Hcls1, Fbxo40 | Mm_Celera | 16:36963374 | CTTTTTTTAATTTGT[C/T]TGTACCTTAGCCCCA | 15163 |
rs221598502 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36952772 | GCCCCCACCTCCCAC[A/C]TCATCTAACCTCTAA | 15163 |
rs221748240 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36948978 | ATCACTAAACTCGGA[A/C]TAAGACTTTCTTAAG | 15163 |
rs221754612 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36940149 | TTTTTATTTCATTTA[C/T]TTATTTTTATATGTA | 15163 |
rs221796424 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36940866 | GAGCTTTATCTGATT[G/T]CTATCCCCAAAACCT | 15163 |
rs221915825 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36962321 | AGGAATCTCCCCTCT[A/G]TCTGTTTGCCTTCTC | 15163 |
rs221961065 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36943880 | TAGGCCTCCAACTGC[A/G]TGTTCCTTCAAAAGC | 15163 |
rs222085658 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36957187 | GATCCCGGACACCCT[A/T]AATTTTCCTTGTTTG | 15163 |
rs222186045 | in-del | -/ATA | | | intron-variant | Hcls1 | Mm_Celera | 16:36950881 | GATTCATTTAATATT[-/ATA]ATATCAAAGAGCCAG | 15163 |
rs222346664 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36951505 | AGAAACATTTTAGCG[A/G]TATTCTTTCTACCAT | 15163 |
rs222630682 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36947055 | CTAGATCAGGTTGAT[C/T]TGTGGGCATGTCTGC | 15163 |
rs222650665 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36946204 | TCTGTAATATTTTAA[C/T]CATTAGACATTAAGC | 15163 |
rs222657088 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36936201 | TCACAGTGACTCTGG[C/T]CACGGTAACTCACCA | 15163 |
rs222689941 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36953116 | ATGCTGCACTTGACC[A/T]ATTCTATGTATATTT | 15163 |
rs222947495 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36956429 | CCTTCTGTCTTCCAA[A/G]AGACAATATTGGAGG | 15163 |
rs223012230 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36940949 | CAAATGGCTGTATTG[C/T]ATACCACGTCATTTT | 15163 |
rs223021113 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36949042 | AAGCGAATACGACAG[C/T]CAATTGATTAGGGCT | 15163 |
rs223135309 | in-del | -/TTGCCCAG | | | intron-variant | Hcls1 | Mm_Celera | 16:36949673 | TTCTCCTGGTCCTCT[-/TTGCCCAG]TCCCTTATTGTTAGT | 15163 |
rs223292661 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36953541 | CAGATATCCTGAGCA[C/T]GGGGTCTGCAGTAGA | 15163 |
rs223351788 | snp | C/T | | | utr-variant-3-prime | Hcls1 | Mm_Celera | 16:36962769 | CAGCCCATTGTCTTC[C/T]GACTTCCCGAATTCG | 15163 |
rs223508596 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36951299 | GTTTGGCTACTTTGC[A/G]GTTCCAATTGTGGGC | 15163 |
rs223520660 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36938815 | GTTTCCTAGCACTGC[A/G]TGGTGGAGGGAGGTG | 15163 |
rs223557694 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36950019 | TAGAGAGGCAACATC[A/G]TCTGCTCCCAAAGAG | 15163 |
rs223674576 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36946336 | TAATTGGTTGAAGGC[A/G]GGTCTTTTGTTAGCA | 15163 |
rs223679779 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36943221 | TCTGTGGGTATGCAG[A/T]GATGTTAATTTGTGT | 15163 |
rs223723562 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36947117 | GGGAAGACCCAGCCT[C/G]CTGTGGATGGCACCA | 15163 |
rs223754886 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36943114 | CCAAAAAGAAATTTG[C/T]CATAGATCATTTCTA | 15163 |
rs223926079 | snp | C/T | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934461 | CCTCCACGTTCTGCC[C/T]TCTCCCTTCCTCGTG | 15163 |
rs224043581 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36935821 | CATCAGGTATTGGAT[A/G]TGCCCAGCATTCATT | 15163 |
rs224130218 | in-del | -/AGA | | | intron-variant | Hcls1 | Mm_Celera | 16:36942659 | ATACGGTGAGGACAG[-/AGA]AGATTTCAGGCACAC | 15163 |
rs224217637 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36942264 | TGATTTTAACAATTT[A/G]TCTAAGGCTATAGAC | 15163 |
rs224352365 | in-del | -/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36944827 | TAAAATATTTTGTAC[-/T]TTTTTTTTTTTTGGT | 15163 |
rs224374354 | in-del | -/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36938694 | CAAGAGAACTTTCTC[-/T]TTTTTTTTCTGAAAT | 15163 |
rs224400333 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Hcls1, Golgb1 | Mm_Celera | 16:36933181 | AGGAGAAAGTTCTGA[A/G]ACTCCTTCATCTCAC | 15163 |
rs224457699 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Hcls1, Golgb1 | Mm_Celera | 16:36933216 | CAGCACCACATGGCT[A/G]TGAACATCCTTCTAG | 15163 |
rs224544649 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36960946 | CCAGGCTGCTTCTAA[A/G]TTCCTGTGTCTTGAG | 15163 |
rs224592715 | in-del | -/TGTT | | | intron-variant | Hcls1 | Mm_Celera | 16:36942975 | CAAATATATTCTGAG[-/TGTT]TGAGCACATCTCTCT | 15163 |
rs224605495 | in-del | -/AG | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934181 | GGAATGGAGGGTGGA[-/AG]AGCAGGGAGGTGGTT | 15163 |
rs224709960 | snp | C/T | | | synonymous-codon | Hcls1 | Mm_Celera | 16:36962203 | GGATGTGCTGGAGCC[C/T]GAGGACACCCCTTCT | 15163 |
rs224731015 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36943456 | CTCTTTTAATTTTCT[A/G]GTGGTATTGTTTGAA | 15163 |
rs224854014 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36944265 | ATCGACTTTGATAAT[A/G]GCGACTCTGTATCCT | 15163 |
rs224955562 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36939495 | ATGGCAAGTAAGTCC[C/T]GTTGTTACATTGTTC | 15163 |
rs224960139 | in-del | -/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36939843 | CCCCAGGCTGCCATA[-/T]TTTTTAGGATCAAGG | 15163 |
rs225391526 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36961140 | GAACAGAGTCTATTA[C/T]ACTTGTCTTTGCAAA | 15163 |
rs225514575 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36962506 | GGGGTGGGTTCTGAG[A/G]GTCAAGAAAGGACCT | 15163 |
rs225574936 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36951970 | GTTTCCGGATCATTA[A/T]TTTAAGGCTATGAAA | 15163 |
rs225843195 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36958625 | GTTCAGCTTCCATGT[G/T]TATGTGGACTTTCTG | 15163 |
rs225982277 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36939622 | TGAGATCAGGCAAAA[C/G]ATTCAAAATCTTAGG | 15163 |
rs226061881 | in-del | -/AAGA | | | intron-variant | Hcls1 | Mm_Celera | 16:36942660 | ACGGTGAGGACAGAG[-/AAGA]AAGATTTCAGGCACA | 15163 |
rs226065215 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36955513 | ACTGATGGAATGGAC[A/G]GTGGGATTGGAAGTG | 15163 |
rs226083259 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36940228 | GCCCATGGTACAGAT[C/G]CTCTGGAGCTGGAGT | 15163 |
rs226325224 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36956867 | AGAGACACGCAGGGA[A/G]GAGAGAGGAAATGCC | 15163 |
rs226424760 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36957480 | ACAGGTGTCTCAGAG[A/G]CCCAAGTGATAGGCA | 15163 |
rs226438103 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36960770 | AGCTCAGGGTGGTTC[C/T]CTCTTGGGCCAGCAA | 15163 |
rs226671771 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36957806 | AGACAGAAACTGTTC[C/T]ATCTCCAAGGGAGAA | 15163 |
rs226760737 | in-del | -/ACTGTCTCTGGG | | | intron-variant | Hcls1 | Mm_Celera | 16:36951054 | TGGGGGGTTCCTAAA[-/ACTGTCTCTGGG]ACTGAGATGGAAGTA | 15163 |
rs226870867 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36943378 | TGAGTTCCCTGTATA[G/T]TTTAGAAACAGATCT | 15163 |
rs226990323 | snp | A/C | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36933901 | ATCCCCTGGGAAGTG[A/C]CTTTAGATGCTTTCT | 15163 |
rs227221504 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36951194 | CTCAGAAAGGCAAGT[A/G]CCCAGAGCCTTGGCC | 15163 |
rs227225458 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36953772 | GCGCGCGCGCGCGTC[C/G]TATGCACATAGAGTC | 15163 |
rs227231631 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36949313 | ATGGGGAGGGGAAGC[A/G]AGAAGAGTAGGAAGG | 15163 |
rs227266277 | in-del | -/GTGCTGTGAACA | | | intron-variant | Hcls1 | Mm_Celera | 16:36941844 | GTCAGCTCCCTGACT[-/GTGCTGTGAACA]GTGCTGTGAGCATTA | 15163 |
rs227302800 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36946418 | AACAGACAACAGGAT[C/G]TTAGCTTCTCGAGAG | 15163 |
rs227586529 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36954531 | TTGAAAACAAAATTA[C/T]ATTCCCCAATTGAAC | 15163 |
rs227659717 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36936375 | CTTGGGGATGAGTGG[A/G]TAAAGGTGTCTCCTT | 15163 |
rs227692428 | in-del | -/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36954828 | GCCAGGATTCTTTCC[-/T]CTCCCCTTCCCCTCC | 15163 |
rs227694805 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36945420 | CCAGACCCTTGCTAA[C/T]TGCAGAAAGCTGGAT | 15163 |
rs227734868 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36954537 | ACAAAATTACATTCC[A/C]CAATTGAACACAGGG | 15163 |
rs227872972 | in-del | -/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36951040 | CCTGTGAACCTTGCT[-/G]GGGGGGTTCCTAAAA | 15163 |
rs227943340 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36955591 | GGCCAGGTGATGGGC[C/T]GAGATGGCTTGGTGT | 15163 |
rs227991038 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36939575 | GAAGCAGGTTTAACA[G/T]GCTAAGTGTTAAGTA | 15163 |
rs228117302 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36955684 | ACAGCTAAATGGCTC[A/G]CCTTGTTTTCCTGTT | 15163 |
rs228136910 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36950382 | GATCTCATCCAGGAC[C/G]GCTCTCCCTGCTATC | 15163 |
rs228179536 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36948754 | TGGCCCATGCTTCTC[A/G]GGTGACAGACAGGAC | 15163 |
rs228180930 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36956656 | GTTAGTCTTCATGGT[A/T]CCCTTCTCTGTGCCC | 15163 |
rs228202549 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36953012 | TTTCAGCCTTCCCTA[A/G]TTCAACAGCAGGGGT | 15163 |
rs228272012 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36947641 | GAGGTCACCACAACA[C/T]GAGAAACTGTATTAA | 15163 |
rs228417273 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36954889 | TTCCCTTCTCTTCTT[C/T]CTCTTCCTCCTTTCT | 15163 |
rs228425152 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36937523 | GATTTTATTAGTAGG[A/G]ATGTGTGTTAGCTGA | 15163 |
rs228429451 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36960534 | TCTGTTTCTTATGTT[A/C]TTGCCCTTGCCGTTT | 15163 |
rs228519456 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36947739 | TGGTATATGCATATG[C/T]TGTATATGGTGCATA | 15163 |
rs228690916 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36941472 | AAGCAATTCTACCCG[A/T]CTCTTATCAGTGTAT | 15163 |
rs228902967 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36952078 | ATTATATCATCATTC[A/G]GGGTCTCTCATGTCA | 15163 |
rs228910609 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36952224 | ACTGAGGCAAGGAAA[C/T]TGCAAGTTCAAGGCC | 15163 |
rs228954947 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36944406 | GCCTTTATTGCTCCT[G/T]TTTCACATTGGAAGC | 15163 |
rs228956058 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36952912 | CAAGCTGTCTGTTTG[C/G]TGGTCCAGTGTTTGA | 15163 |
rs228963078 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36950577 | GAAACCCATAGTTAC[C/T]GAGCAAATGGGGATA | 15163 |
rs229024832 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36961042 | CCTGGGAGACCAGCT[C/T]TCTCCCAGTGGTATT | 15163 |
rs229054272 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36945233 | CTCTAAAATTAACCA[C/T]GGCTAAAGCTGAAAG | 15163 |
rs229220103 | in-del | -/A | | | intron-variant | Hcls1 | Mm_Celera | 16:36950776 | TTCCTTGTGTGACTC[-/A]AGTGCAGGTACTGTA | 15163 |
rs229528145 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36951233 | CCAGCTTCCCTGCCC[A/G]CATCTGCTGCCTACA | 15163 |
rs229550580 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36951284 | TCCAGCTCCCCACTG[C/G]TTTGGCTACTTTGCG | 15163 |
rs229558437 | in-del | -/ATC | | | intron-variant | Hcls1 | Mm_Celera | 16:36960402 | CTTCTTAAAGTCCCT[-/ATC]ATCATCATCATGAGA | 15163 |
rs229613127 | snp | C/T | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36933606 | CCACTTGGGAAAAGC[C/T]GACCCAGTATCACAG | 15163 |
rs229652723 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36943612 | GATTATCTCAAACAT[C/T]TGGCTCAATTTAAAA | 15163 |
rs229840906 | in-del | -/TTAGAATCCAA | | | intron-variant | Hcls1 | Mm_Celera | 16:36940765 | ACAGCTACTCTGGAT[-/TTAGAATCCAA]TGAATAGTATATGTG | 15163 |
rs229855961 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36943762 | TGACCTTCTGTATGG[C/T]TGACTTTTGGACTCT | 15163 |
rs229925097 | in-del | -/A | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36933693 | AGCACTGTTCTGCTC[-/A]AGGGATGAACATGGG | 15163 |
rs229940242 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36952470 | ttatcaattgtttat[A/C]tgttcttaaaataca | 15163 |
rs230196046 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36936173 | TGGGGGAGGCACAGA[C/T]GTTCTTAATAGCTCA | 15163 |
rs230252725 | in-del | -/TA | | | intron-variant, utr-variant-3-prime | Hcls1, Fbxo40 | Mm_Celera | 16:36963675 | ATCAACCACTAATTT[-/TA]AAAATGCCTTACAGA | 15163 |
rs230356520 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36945047 | GCCATTCAGAAGCTC[C/G]GGGCGCCCGCCCGCC | 15163 |
rs230447956 | in-del | -/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36961788 | TCCATACATGCCCCT[-/C]CCCCCCCTCATACCT | 15163 |
rs230486666 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36944302 | TTAGTGGTTCCAGTA[A/G]CTTCTTTGTGGATAA | 15163 |
rs230543675 | snp | G/T | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934064 | AGTTCTTAGTAGGAT[G/T]ATTTTTCAACCAGAG | 15163 |
rs230546981 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36941951 | GGCTTAGCCAATATT[A/G]TGCCCTACAACTTTA | 15163 |
rs230565587 | snp | C/G | | | upstream-variant-2KB, downstream-variant-500B | Hcls1, Golgb1 | Mm_Celera | 16:36933312 | AGGAGCAGAACCATA[C/G]GATGTAAATTTGTGA | 15163 |
rs230678239 | in-del | -/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36945096 | TTCAGACCCTGGCAG[-/C]CCCAAGGCTGTTGAG | 15163 |
rs230737374 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36948434 | CTGGTACCACTGCCA[A/G]AGGTACCAAGAATGG | 15163 |
rs230929190 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36942761 | CATGTGGCATAGGTA[C/T]TAGGGTCTCTCTAAA | 15163 |
rs230930985 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36941602 | CCTTAAACTCTCTGT[G/T]GGAGAGGACAAATGC | 15163 |
rs230973587 | in-del | -/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36952077 | TATTATATCATCATT[-/C]AGGGTCTCTCATGTC | 15163 |
rs231028840 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36952935 | GTGTTTGAGAGATCT[C/T]GGGGGTCTAGATTAA | 15163 |
rs231125372 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36951246 | CCGCATCTGCTGCCT[A/G]CAGCTTGTCATAGCT | 15163 |
rs231280221 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36942469 | CTCTTTAAAGCCGCT[A/G]AGTATATTTAGTCCG | 15163 |
rs231299755 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36949764 | CTAAAGGGTGGGGAC[A/G]TAGCTCCGTTGGAAG | 15163 |
rs231499457 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36940260 | ACAGATTGTTGTAAG[A/C]TGTCATGTGGGTGCC | 15163 |
rs231509115 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36961953 | GCAACCTCATTAAAC[C/T]ATCACTGAATCTTCC | 15163 |
rs231564055 | snp | C/T | | | utr-variant-3-prime | Hcls1 | Mm_Celera | 16:36962879 | TGGCAGTCTGTCTCC[C/T]GCCTCTTTAAGAGCT | 15163 |
rs231565353 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36951660 | ATCAAGGCCAGCCTA[G/T]TCTACATAATAATTC | 15163 |
rs231576696 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36952696 | AATTTTTTATTCTAT[A/G]TTTTTTCAACTGCTC | 15163 |
rs231692938 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36958154 | CTGATGATTTTTAAA[A/C]ATTTCTTGAGTTTCT | 15163 |
rs231695477 | in-del | -/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36947685 | TAGGAAGGTTGAGAA[-/C]CACTGCTTTACTGTG | 15163 |
rs231705359 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36960699 | TCAGCTCCACAGTGC[A/G]GTGGGAAACCAGAAG | 15163 |
rs231841129 | in-del | -/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36937951 | GCAGGCTGGGGCTCA[-/G]GGGGTGCAGAAAGGA | 15163 |
rs231923770 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36955159 | GCCTATCACTCTGCA[C/T]TCCTTCCTTCAGACC | 15163 |
rs232033526 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36942612 | AATAATTATAAACCA[A/G]TGAATTTTGATAACA | 15163 |
rs232042765 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36947291 | CCTGGAATGGTAGCC[A/C]AATAAAACCTCTCTC | 15163 |
rs232238140 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36950198 | TTGAAATTGCAGGGA[A/T]GAAAGCCCACAGACT | 15163 |
rs232414140 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36959267 | GCAAAATGCTGAGTA[C/T]TGTTTATGTATCCAG | 15163 |
rs232444669 | in-del | -/G | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934781 | TCCTGCAGCATTCTT[-/G]ATTGTGTCTTAACTG | 15163 |
rs232539492 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36956172 | TATGAATTCCACACT[C/T]TGAGGTTTAAGTTAG | 15163 |
rs232639206 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36948955 | TCAATGGTCACTCAT[A/G]GGTAAAGATCACTAA | 15163 |
rs232662736 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36935887 | TTCCTGATTAGTAAT[C/T]GACAGTACAAGAATA | 15163 |
rs232695383 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36949484 | GACTGAGTCCAAGTT[A/G]GGAAGTGCTAGGATT | 15163 |
rs232964529 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36954700 | AGGACAGATCCTAGG[C/T]CCTAATCCCTATTCC | 15163 |
rs233060762 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36949880 | CCACAGATCCATTTG[C/T]CCGTCAAATAAAGAA | 15163 |
rs233119294 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36946555 | CAGTCTGTCGATCTC[A/C]CTGACTGTGGAGAGT | 15163 |
rs233482122 | in-del | -/GCTCCCTGAGC | | | intron-variant | Hcls1 | Mm_Celera | 16:36940433 | AGGAGTTTCCCAGAA[-/GCTCCCTGAGC]GCTCACAGATGAAGA | 15163 |
rs233510166 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36956755 | ATTAGCCAAGAAAGA[C/T]GAGCTCCCTGCTCTC | 15163 |
rs233654523 | in-del | -/TT | | | intron-variant | Hcls1 | Mm_Celera | 16:36938001 | CTTTGCATTTATTTA[-/TT]TTTTTCTAGAATCTC | 15163 |
rs233962192 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36953058 | ATTGGGACTCTCTTT[A/C]TGATACAGGTAAATC | 15163 |
rs234118053 | snp | C/T | | | missense | Hcls1 | Mm_Celera | 16:36957364 | GAAGTCCAGCAGCCA[C/T]CCATGCCTGTGGAAG | 15163 |
rs234136505 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36946804 | TTGGTACTTTAAAAT[G/T]TATCCTAAATATGGT | 15163 |
rs234192438 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36936055 | CCAGTTTCCTTCTGT[G/T]GTAGAGTAGCCTGAG | 15163 |
rs234300760 | in-del | -/CC | | | intron-variant | Hcls1 | Mm_Celera | 16:36945716 | TGTCCTAAGAGTCTG[-/CC]CCCCCCCCCCCAAAT | 15163 |
rs234821093 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36947826 | CACAGCAGGATGTCA[A/G]ATGTCATCCTGTACA | 15163 |
rs234829040 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36946907 | TCAATACCCAAGATA[C/T]AGAAAAGAGAGTCAA | 15163 |
rs234839025 | in-del | -/A | | | intron-variant | Hcls1 | Mm_Celera | 16:36942477 | GCCGCTGAGTATATT[-/A]TAGTCCGGCTTTAAC | 15163 |
rs234949172 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36949592 | GAAACCATGTTTAAA[A/G]TCAATAATGCCATGT | 15163 |
rs235012854 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36962604 | CTAATGTCTCCTCAA[C/T]TTCCTCCCCAGAGGG | 15163 |
rs235142333 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36949535 | CAGCCAAAACAAAGT[C/T]AAGAAAATTCAAAAT | 15163 |
rs235156561 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36954311 | CCTGTCTCTGCCTCT[A/C]CAGCGCTAGAATCCC | 15163 |
rs235177219 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36955013 | TTGTCCCAGAGATGA[C/T]CTCTCACGGGCTCTA | 15163 |
rs235238248 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36952723 | GCTCCATATCCCACA[C/T]CTCCTCCCCTCCCAA | 15163 |
rs235367604 | snp | A/G | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934213 | TTTGAAAGGCAGCCA[A/G]TAAAAGCATAGCAAA | 15163 |
rs235389603 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36946059 | ACACAAATACTAGTA[A/C]ATTTACCCCAAACTA | 15163 |
rs235441541 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36957072 | TCTCACTACCTCTGT[A/G]CCTTCCCCTCCACAC | 15163 |
rs235556941 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36939899 | GGTGAAAGTTGGAAA[A/G]TCATGAATCGGCACT | 15163 |
rs235581541 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36960788 | CTTGGGCCAGCAATT[A/T]GAGCAGAAGTGGTGG | 15163 |
rs235860946 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36942118 | TCTCCTTACCTCGCC[A/G]TGAAGAGCCGCGGCT | 15163 |
rs235917437 | snp | G/T | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934019 | CACAGATGACTGGGA[G/T]AAGGAGAGCCAGGCT | 15163 |
rs235928633 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36947865 | CCTTAGCCCCTTGGG[A/G]CCGGCTTTCCCTCTG | 15163 |
rs235987665 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36938840 | GAGGTGGCTGTGGGA[A/G]AGTAATGGATGCTGA | 15163 |
rs235999720 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36948795 | ATCAGTGCCTAGTAA[C/T]GGTCAGGTCTCATGA | 15163 |
rs236019147 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36943665 | TGCGGCATGCAATTG[A/G]GTTAAGGCTCTTCTT | 15163 |
rs236101053 | in-del | -/TTAATGTAC | | | intron-variant | Hcls1 | Mm_Celera | 16:36943339 | TATATTTACTCAGTT[-/TTAATGTAC]TTAATGTACTTTTAT | 15163 |
rs236290622 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36946191 | TGGTTTTCTATTATC[C/T]GTAATATTTTAATCA | 15163 |
rs236329941 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36940178 | TATGGGTCTTTTTTC[A/G]GTATACGTGTTTATG | 15163 |
rs236340753 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36950615 | CAGTATATATTAGGT[C/T]TTGGAACCTACAAAA | 15163 |
rs236404572 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36943120 | AGAAATTTGTCATAG[A/T]TCATTTCTACCAGAA | 15163 |
rs236404640 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36951398 | AGGGTAGAAGATATA[G/T]TTCTTTTTTGTTCTA | 15163 |
rs236432064 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36950828 | ATTATTCCAAATGAG[G/T]AAAGATCATGTCCCT | 15163 |
rs236432995 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36940924 | TCCTACTTCCTAAAT[A/G]GCTTTTAATCAAATG | 15163 |
rs236648566 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36951949 | ATTTTCCTCTTGCTG[A/G]AATATGTTTCCGGAT | 15163 |
rs236668461 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36948996 | AGACTTTCTTAAGGC[A/T]TTAGCAGAGAGGAGA | 15163 |
rs236810021 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36957888 | TTTCTATTTTGTGGA[A/G]TAGTTTGAAGAGTAT | 15163 |
rs236985655 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36962334 | CTGTCTGTTTGCCTT[C/T]TCCATGTTGATGTTT | 15163 |
rs236992538 | in-del | -/TATATATAC | | | intron-variant | Hcls1 | Mm_Celera | 16:36951533 | CATCTATATTACTGT[-/TATATATAC]TGGCTAGTATATTGT | 15163 |
rs237032752 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36943200 | GGTATTTTGAATGTT[A/G]GCCACTCTGTGGGTA | 15163 |
rs237098807 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36959556 | TGGGGAAAGATATTA[C/T]GTAAATTTGTTTCTG | 15163 |
rs237237134 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36948904 | TAGGGCAGCTCTGGC[C/T]TAGCATAGGAGAGGC | 15163 |
rs237390168 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36939973 | ACTCCTCCTTCCACA[A/C]ATGACAATATTTTAG | 15163 |
rs237407846 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36961578 | CCAGAGATTCTCTGT[C/G]CCCACCTCATCTTCG | 15163 |
rs237458437 | in-del | -/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36951850 | TATATATATATATAT[-/G]ATACCAATGAATAAT | 15163 |
rs237483501 | in-del | -/TG | | | intron-variant | Hcls1 | Mm_Celera | 16:36941085 | TTAAAGCCTTCTACA[-/TG]CGCAAAAGCTGGGAC | 15163 |
rs237563212 | snp | C/T | | | downstream-variant-500B | Hcls1, Fbxo40 | Mm_Celera | 16:36963435 | TAAGGTTTTTAGTGC[C/T]AGGATAAAGTACATG | 15163 |
rs237593029 | in-del | -/AATCCACCATGA | | | intron-variant | Hcls1 | Mm_Celera | 16:36953507 | TCAAACAATTTATGG[-/AATCCACCATGA]AATCCACCTCATGTT | 15163 |
rs237605916 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36950572 | ACTTAGAAACCCATA[A/G]TTACCGAGCAAATGG | 15163 |
rs237626808 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36950857 | CTCAATTTACTGTCG[G/T]GGTGGGTAAGATTCA | 15163 |
rs237751599 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36942902 | CCCGTTACTGTCAAA[A/C]AGTATCTATTGTGTA | 15163 |
rs237953086 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36958877 | TATTAGTTTCAATGT[A/G]TCTCTGTTCAGTTTC | 15163 |
rs237964851 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36950217 | AGCCCACAGACTCCA[C/T]AGGGGTCTCATTTTC | 15163 |
rs237965966 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36960903 | AGGGTCAGCTCTGGG[C/T]GCAGACGGACACTTG | 15163 |
rs238096446 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36949943 | CATGAGATTCATTGC[A/C]GCAGAGCTAGCACAC | 15163 |
rs238111847 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36940809 | TGGCCCTCTTAGTAC[A/T]ACTTAGCACTTTGGT | 15163 |
rs238242967 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36942403 | AATTCTCTTTTGAAA[G/T]GCAATCTGAATTCCC | 15163 |
rs238480560 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36949608 | TCAATAATGCCATGT[A/G]GAGCTTGTAAGGATC | 15163 |
rs238594946 | in-del | -/GCA | | | intron-variant | Hcls1 | Mm_Celera | 16:36943825 | GCACACTACCACAGT[-/GCA]GCTGTTATTATAGCT | 15163 |
rs238640562 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36945565 | GCTGTCAACTCATGT[C/T]TTCAGGATGTCTACC | 15163 |
rs238701198 | snp | C/T | | | utr-variant-5-prime | Hcls1 | Mm_Celera | 16:36934998 | GAGCAGCTGCTCTGT[C/T]ACTTACCCTGAAGTG | 15163 |
rs238760390 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36957127 | CTGTATATCTAACAG[A/C]TCTCGCTCATTTATA | 15163 |
rs238825957 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36938288 | TAAACTTTTACAGAA[A/G]TGTAGAACATGTGTA | 15163 |
rs238834704 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36948133 | GTGATCTTTTATATA[A/C]ACATTGGAAAGTTCA | 15163 |
rs238835252 | in-del | -/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36941468 | GCTTAAGCAATTCTA[-/C]CCGTCTCTTATCAGT | 15163 |
rs238874180 | in-del | -/CT | | | intron-variant | Hcls1 | Mm_Celera | 16:36940673 | TGATTTCGTTCCCAG[-/CT]CTGTCATCATTAGTG | 15163 |
rs239037399 | in-del | -/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36955760 | TCTTTCCATTCCTTT[-/C]TTTTCTCTCCCAACC | 15163 |
rs239172868 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36953140 | TATATTTCAATTTTA[A/G]TTAAATTAAAACATT | 15163 |
rs239212417 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36947302 | AGCCAAATAAAACCT[C/T]TCTCCTTTCAAGTTT | 15163 |
rs239212475 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36955489 | AAGAGGGGCATGAGG[C/G]GGCTCAACACTGATG | 15163 |
rs239220240 | in-del | -/CTA | | | intron-variant | Hcls1 | Mm_Celera | 16:36935588 | GAGGGAGCTTTGGAT[-/CTA]CTGTGTTAACCCCTT | 15163 |
rs239406664 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36949471 | GTTAATTAGGTAGGA[A/C]TGAGTCCAAGTTGGG | 15163 |
rs239491625 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36936813 | AGTAGTTCAACTAGT[C/T]TGTCCCACTGGTGAC | 15163 |
rs239499290 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36940671 | TTTGATTTCGTTCCC[A/T]GCTCTGTCATCATTA | 15163 |
rs239614571 | in-del | -/CACGGTA | | | intron-variant | Hcls1 | Mm_Celera | 16:36940953 | GGCTGTATTGCATAC[-/CACGGTA]CACGTCATTTTCACA | 15163 |
rs239745401 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36955124 | AGCTCACCTCTACCC[A/G]AGCCCAGAGCCCTTC | 15163 |
rs239855929 | in-del | -/AAATCTTT | | | intron-variant | Hcls1 | Mm_Celera | 16:36939236 | ATGGATGCTTAGCAG[-/AAATCTTT]AACTATCAGCAATAA | 15163 |
rs239910440 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36956458 | GGCCCCAGTTCAACT[A/G]TTGCTTACCACATGG | 15163 |
rs239966662 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36939407 | ACATGCATTAGTCTG[G/T]GTTGGGGACGTGGAA | 15163 |
rs240113282 | in-del | -/G | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36933968 | ACCTGGGACCCTTGT[-/G]GGGTTCATTCTCTGT | 15163 |
rs240113716 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Hcls1, Golgb1 | Mm_Celera | 16:36933437 | AGGAGGACCATAAGT[C/T]CAAGGCCAGTCTTGT | 15163 |
rs240238956 | in-del | -/GA | | | intron-variant | Hcls1 | Mm_Celera | 16:36952486 | GTTCTTAAAATACAT[-/GA]GGTTTTGACTCTATT | 15163 |
rs240269537 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36961320 | CTCCATCACCTTCCA[C/T]GTGGTACCCATCTTG | 15163 |
rs240342227 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36941720 | AGAAAATACAAGCAC[A/G]ATTTTTATCTTGTAA | 15163 |
rs240479680 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36953185 | GTGAATTTTCTCTGA[C/G]ATAAATTGTTTGAAA | 15163 |
rs240627728 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36956692 | CCTCCTTTCTCTTCT[A/G]GCTTCCTCTCCTCCC | 15163 |
rs240676739 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36950038 | GCTCCCAAAGAGCCT[A/G]AGTTTGTAGACGTGT | 15163 |
rs240820080 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36944697 | AGCTATATGGTAAAG[A/G]AATTTATAAGAAGTT | 15163 |
rs240977992 | in-del | -/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36943536 | TTTATCATTAGTGGG[-/T]TTTTTTGGTTTATTT | 15163 |
rs241014290 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36962521 | GGTCAAGAAAGGACC[C/T]AGAAGACCAGGTCTG | 15163 |
rs241075954 | snp | A/T | | | intron-variant, utr-variant-3-prime | Hcls1, Fbxo40 | Mm_Celera | 16:36963635 | CCAGGGATGGTTACC[A/T]CCCACAGCAGGCCAG | 15163 |
rs241082743 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36952868 | AGTCCTCAACTGTAT[A/G]TGTGTTGGGGGCCTC | 15163 |
rs241110603 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36936267 | AGATGTCTTCGGGGC[G/T]AATCTTCTAGAGGTT | 15163 |
rs241476926 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36953409 | ATGTTCTTTCTCTTT[C/T]ATGGAACAAACGAAC | 15163 |
rs241597314 | in-del | -/ACACAC | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36951748 | CAAAGCCATACACAT[-/ACACAC]ACACACACACACACA | 15163 |
rs241604211 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36944113 | TTTGAGTTAGTTTTT[C/T]AGAAGTATTATTCAG | 15163 |
rs241628300 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36947056 | TAGATCAGGTTGATC[G/T]GTGGGCATGTCTGCT | 15163 |
rs241648911 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36952810 | GGAGCCTCCAGTCTC[C/T]TGAGGGTTAGATTCA | 15163 |
rs241661575 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36945036 | GACCTCACACAGCCA[A/T]TCAGAAGCTCCGGGC | 15163 |
rs241715439 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36944867 | TTTCATTTAAAAACT[A/G]TCATCTGTTGGTACA | 15163 |
rs241802237 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36946368 | AGAGGGCTCATTGGT[C/T]CTGTGACACACAGGT | 15163 |
rs241877103 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36935107 | GGGGTTTTGTGAGGG[C/G]TTGGGAGCACAGGGA | 15163 |
rs241909832 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36951210 | CCCAGAGCCTTGGCC[A/G]CGGCTGGCCAGCTTC | 15163 |
rs241919217 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36951883 | AATTGGGTAACAATG[C/G]ACACCTTCTTAGCTA | 15163 |
rs242073795 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36955524 | GGACAGTGGGATTGG[A/G]AGTGAAGCAGAAAAG | 15163 |
rs242121646 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36942789 | AAAGTTTCAGTAAAT[A/G]AATAACAAAGACTGT | 15163 |
rs242229083 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36935618 | CTTAATTATTTAACA[C/T]TGGGAAACAATATCA | 15163 |
rs242239686 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36947127 | AGCCTGCTGTGGATG[G/T]CACCATTCTCTAGGC | 15163 |
rs242338840 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36936530 | TACCTCTCCTCAAAA[A/C]CCCACAGTGTGACCG | 15163 |
rs242466302 | in-del | -/AG | | | intron-variant | Hcls1 | Mm_Celera | 16:36940407 | GAGTGACAAAGAAAA[-/AG]AGCAGAAACAAGGAG | 15163 |
rs242523399 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36955906 | GCTGCTCCCTCTCCC[C/T]ACCAATTCCCAGCCT | 15163 |
rs242604958 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36943472 | GTGGTATTGTTTGAA[C/T]GGCACAAGATTTGAA | 15163 |
rs242619246 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36950072 | CAGGCTGTGGAGCAA[A/C]GCTTGTTTCCATTTC | 15163 |
rs242636618 | snp | A/G | | | synonymous-codon | Hcls1 | Mm_Celera | 16:36957381 | CATGCCTGTGGAAGA[A/G]CCAGCGGCACCAGCC | 15163 |
rs242678509 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Hcls1, Golgb1 | Mm_Celera | 16:36933253 | CTGCTGGAGCCAAAG[A/G]AGATGAGGTTCAGAT | 15163 |
rs242773413 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36949355 | GAGACAAAAAGGAGA[G/T]GTGGGGGGGATCGAG | 15163 |
rs242867663 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36960721 | AACCAGAAGGATCCT[A/G]TCCCGAGCTGTTCCT | 15163 |
rs242932388 | in-del | -/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36946834 | TTTGCATGGTGTCCA[-/T]TTGGGCTTTGATGCA | 15163 |
rs242984786 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36947717 | TATGTGATTATTTGT[A/G]TATGCATGGTATATG | 15163 |
rs243047811 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36937680 | TAATTTTAATTTTCA[A/T]GTGGCTTTGAGATAA | 15163 |
rs243059364 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36939598 | GTTAAGTAGTGTCAA[C/T]TTTGGTTATGAGATC | 15163 |
rs243091281 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36950466 | TTGCCTACAGAGAGA[A/G]TCTGAGGTCAGCCTT | 15163 |
rs243104593 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36940229 | CCCATGGTACAGATG[C/T]TCTGGAGCTGGAGTT | 15163 |
rs243186612 | in-del | -/TCTA | | | intron-variant | Hcls1 | Mm_Celera | 16:36943716 | AAACACAATCCAAAC[-/TCTA]TCTTTTTCCCACTGA | 15163 |
rs243271163 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36961087 | TGTGGCACAGGATCA[A/G]CTACGGGTGCACATG | 15163 |
rs243356089 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36944068 | TCCAATCTATGAACC[C/T]GTGGCATTCCTCTAC | 15163 |
rs243359190 | in-del | -/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36954676 | CCCACTCTTGTATAG[-/T]AGTTGATAAGGACAG | 15163 |
rs243364063 | in-del | -/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36943632 | CAATTTAAAATTTTA[-/C]TTTTTTTAATATTTA | 15163 |
rs243515830 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Hcls1, Fbxo40 | Mm_Celera | 16:36963058 | GTGCTGGGATTCCCT[C/T]GCCCCGACCCTGGGT | 15163 |
rs243630974 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36956968 | ATAAAGATGCTGGTT[A/C]AAGGACTCATAATTT | 15163 |
rs243847692 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36947167 | ATAAATGTAGGGACA[G/T]AGAGTTGAACAGTAA | 15163 |
rs244113163 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36957669 | ATGATATCTTCTGAA[A/G]CTAAAAGTATTATGC | 15163 |
rs244220878 | in-del | -/CTCTCTCTCT | | | intron-variant | Hcls1 | Mm_Celera | 16:36955173 | CTCCTTCCTTCAGAC[-/CTCTCTCTCT]CTCTCTCTCTCTCTC | 15163 |
rs244385938 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36940554 | ATGCTGCTTTCCCTC[C/T]CATGTGCCTGCATCT | 15163 |
rs244400034 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36951939 | TGCTGTTTCTATTTT[C/T]CTCTTGCTGGAATAT | 15163 |
rs244437374 | snp | A/T | | | utr-variant-3-prime | Hcls1 | Mm_Celera | 16:36962781 | TTCCGACTTCCCGAA[A/T]TCGAAGCTGCTCTGC | 15163 |
rs244442233 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36941486 | GTCTCTTATCAGTGT[A/G]TAGAGAAATGACCCC | 15163 |
rs244480397 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36944273 | TGATAATGGCGACTC[C/T]GTATCCTGAAAGCTT | 15163 |
rs244887545 | in-del | -/TTC | | | intron-variant | Hcls1 | Mm_Celera | 16:36940473 | AAGGTCAAAGCTCTT[-/TTC]TCCTCTGAGTGAAGC | 15163 |
rs244887820 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36939515 | TTACATTGTTCTCTT[A/G]AAGCAGGTTTAACAG | 15163 |
rs244991774 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36952347 | ACAGAGCATTTGGGT[A/G]GCCTTGACCCACCCG | 15163 |
rs245026456 | in-del | -/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36945717 | TGTCCTAAGAGTCTG[-/C]CCCCCCCCCCAAATA | 15163 |
rs245047700 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36950720 | GCACACAAGGCTTTT[A/G]GTTACAAGGTTGTGA | 15163 |
rs245186704 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36945912 | TAGGAACTTGAAGCT[C/G]TTCTAACAGATAATG | 15163 |
rs245220137 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36950181 | GACCCTGCTGGGGAC[C/T]TTTGAAATTGCAGGG | 15163 |
rs245238929 | snp | A/G | | | synonymous-codon | Hcls1 | Mm_Celera | 16:36946621 | GAGGAACAAAGTGTC[A/G]GAGGAGCACGACATC | 15163 |
rs245507810 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36958405 | TTCTTTTTGTTCTAG[A/G]GCTTTCAAATCTGCT | 15163 |
rs245520654 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36935838 | GCCCAGCATTCATTG[C/T]CTGTCTCCAGCCTCC | 15163 |
rs245823416 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36955011 | TTTTGTCCCAGAGAT[C/G]ATCTCTCACGGGCTC | 15163 |
rs245840841 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36950203 | ATTGCAGGGAAGAAA[A/G]CCCACAGACTCCATA | 15163 |
rs245843393 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36955603 | GGCCGAGATGGCTTG[A/G]TGTAAGTCTCATGGG | 15163 |
rs246160498 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36943248 | GTGTTTCTTGGGTGA[A/G]TAAACCTATTAAGCA | 15163 |
rs246201655 | snp | G/T | | | upstream-variant-2KB, downstream-variant-500B | Hcls1, Golgb1 | Mm_Celera | 16:36933129 | GTTACATGCCTGTGT[G/T]TGCACACTATGGGAG | 15163 |
rs246382096 | in-del | -/AG | | | intron-variant | Hcls1 | Mm_Celera | 16:36954026 | AGGGCTTTTCCTTAT[-/AG]AGTACTTCACAGTGT | 15163 |
rs246614150 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36947948 | TTCGCCTGTCTCTAC[C/T]TTCTCATGCTGGGAT | 15163 |
rs246827549 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36955062 | AGGAGGGAAAATATT[G/T]CGATGCTCATTTGGG | 15163 |
rs246857730 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36946224 | AGACATTAAGCTTTG[C/T]CGTATTTAAAGTTAT | 15163 |
rs246884164 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36955776 | TTTTCTCTCCCAACC[A/C]CCATACCCTGACCCT | 15163 |
rs247057166 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36952048 | TCATGCTATTCCCTT[C/T]ATTATTTTGAAAATA | 15163 |
rs247132012 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36953566 | AGTAGACTGTGACTA[A/G]TGAGCTGAAAGAGCA | 15163 |
rs247190222 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36960708 | CAGTGCAGTGGGAAA[C/T]CAGAAGGATCCTATC | 15163 |
rs247240605 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36961150 | TATTATACTTGTCTT[G/T]GCAAAGATTCAGTAT | 15163 |
rs247245074 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36949883 | CAGATCCATTTGCCC[A/G]TCAAATAAAGAATCA | 15163 |
rs247321438 | in-del | -/TT | | | intron-variant | Hcls1 | Mm_Celera | 16:36946438 | TTCTCGAGAGCGTAA[-/TT]ATCAGGCTACATTGC | 15163 |
rs247579977 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36940089 | GAATGTCTCTGAATA[C/T]GGTAGAGACCTAAAT | 15163 |
rs247728393 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36941816 | TATCTGATTTCATTG[A/T]GGAAAAGAAGCAGGT | 15163 |
rs247772838 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36945323 | CATGAAAGGAGAAGG[C/T]CTCTCCTGTGACACG | 15163 |
rs247790206 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36942679 | ATTTCAGGCACACTA[A/G]CAGTCCTGTGTGTGT | 15163 |
rs247798026 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36943394 | TTTAGAAACAGATCT[C/T]ATGTAAAATGAGTAT | 15163 |
rs247910162 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36940940 | GCTTTTAATCAAATG[A/G]CTGTATTGCATACCA | 15163 |
rs247922395 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36941954 | TTAGCCAATATTATG[C/T]CCTACAACTTTACAC | 15163 |
rs248096426 | in-del | -/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36947944 | AGAATTCGCCTGTCT[-/C]TACCTTCTCATGCTG | 15163 |
rs248274751 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36960844 | GGCACTCCTGGGAGA[C/T]CAGTTATCTCTGGGA | 15163 |
rs248288180 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36961674 | TGGAATCTCCCCAGT[C/T]CTGGGCAAACCTGGG | 15163 |
rs248353118 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36952943 | GAGATCTCGGGGGTC[C/T]AGATTAATTAAGACT | 15163 |
rs248569072 | snp | C/T | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36933909 | GGAAGTGACTTTAGA[C/T]GCTTTCTGTTGGTAC | 15163 |
rs248750472 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36962286 | AAGTTTGGTCAGTTT[G/T]GGGGCAGCAGAGAAA | 15163 |
rs248830782 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36936056 | CAGTTTCCTTCTGTG[G/T]TAGAGTAGCCTGAGA | 15163 |
rs248928708 | in-del | -/TCC | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36933931 | GTTGGTACAGAATGT[-/TCC]TCCCTTCTGTCTAGT | 15163 |
rs249172231 | in-del | -/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36960975 | GGTCTCCAGGCAGGT[-/C]CGTTGGACCTAAAGT | 15163 |
rs249376367 | in-del | -/AATC | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36933881 | GTGCTCCAAGTCTAG[-/AATC]AATCCCCTGGGAAGT | 15163 |
rs249418059 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36955396 | TTGGAAGGAAGGAGG[C/T]CACTAGGTCGCACAG | 15163 |
rs249430168 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36956132 | GGTCCTGAGCCTGGT[A/G]TGCTGGGCTTCAACA | 15163 |
rs249440308 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36945059 | CTCCGGGCGCCCGCC[C/T]GCCCCGCCCCGCCCC | 15163 |
rs249591281 | snp | C/G | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934133 | CAGTGCTCCAGGCTG[C/G]CAGAGGAGCCATGCT | 15163 |
rs249996558 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36949745 | TGTGTTCTGTAAATC[A/C]AGACTAAAGGGTGGG | 15163 |
rs250136695 | in-del | -/A | | | intron-variant | Hcls1 | Mm_Celera | 16:36944468 | AATACAAGCCATGTG[-/A]AAAACGTGAAGCAGA | 15163 |
rs250208718 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36955910 | CTCCCTCTCCCTACC[A/G]ATTCCCAGCCTTCTC | 15163 |
rs250683538 | in-del | -/A | | | intron-variant | Hcls1 | Mm_Celera | 16:36952695 | AATTTTTTATTCTAT[-/A]GTTTTTTCAACTGCT | 15163 |
rs250697488 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36947141 | GGCACCATTCTCTAG[A/G]CCTGTGTTATATAAA | 15163 |
rs250752583 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36942535 | GGACCTCTTTAGGAG[C/T]ACGTAAAAGCCATCA | 15163 |
rs250787729 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36938926 | GTGTTAAAGATACTC[G/T]GAGTTGCCAAGAATG | 15163 |
rs250848988 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36939910 | GAAAATCATGAATCG[A/G]CACTTCTAAACTTGG | 15163 |
rs251011364 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36949472 | TTAATTAGGTAGGAC[G/T]GAGTCCAAGTTGGGA | 15163 |
rs251058342 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36949593 | AAACCATGTTTAAAG[C/T]CAATAATGCCATGTA | 15163 |
rs251333822 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36952595 | cagttgatttgggCT[C/T]tcttttcttttcttt | 15163 |
rs251680680 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36947774 | TATGCACGTGTGGAG[A/G]TGGGGTGGGTGCAGC | 15163 |
rs251690980 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36938237 | AGCTATCACCCATCT[A/C]TACCCTATAAATTAT | 15163 |
rs251782142 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36961015 | ACCTGTGCTCACAGG[C/T]TTGTCAGCACTCCTG | 15163 |
rs251997500 | snp | A/C | | | synonymous-codon | Hcls1 | Mm_Celera | 16:36962074 | GTACGAAGCAGCACC[A/C]GAGCTGGAGCCGGAG | 15163 |
rs252023141 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | Hcls1, Golgb1 | Mm_Celera | 16:36933066 | CTGTAAAATAATAAA[A/G]TTATTTTCAGAATAA | 15163 |
rs252066324 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36952714 | TTTTCAACTGCTCCA[C/T]ATCCCACACCTCCTC | 15163 |
rs252097627 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36960626 | CCTATGTGTAGGTAC[G/T]TCTGGGAGACCAGTT | 15163 |
rs252127362 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36950543 | GAGAGTCTGAAGATG[A/C]GAAACTGACCCTTAC | 15163 |
rs252250042 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36935932 | TCTTAAACATGAGCA[C/T]GAGGGGCTGATGGGA | 15163 |
rs252299059 | snp | A/G | | | intron-variant, utr-variant-3-prime | Hcls1, Fbxo40 | Mm_Celera | 16:36963461 | ACATGACCAAAAGCA[A/G]CTCGGAGAGGAAAGG | 15163 |
rs252708909 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36945011 | TCCTCACTTGGATTC[C/T]TCAGTTGGGGACCTC | 15163 |
rs252717892 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36946082 | CCAAACTACATTTCT[C/T]TAAGCATCAGTCTTA | 15163 |
rs252722050 | snp | A/T | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36933996 | TGTAAGCCAGGCAAG[A/T]CAGAGTCCACAGATG | 15163 |
rs252764947 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36935115 | GTGAGGGGTTGGGAG[C/T]ACAGGGAAGTATGGA | 15163 |
rs252932811 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36944319 | TTCTTTGTGGATAAT[G/T]TAGGATTTTCTAAAC | 15163 |
rs252972547 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36948975 | AAGATCACTAAACTC[A/G]GACTAAGACTTTCTT | 15163 |
rs252979709 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36949485 | ACTGAGTCCAAGTTG[C/G]GAAGTGCTAGGATTG | 15163 |
rs252986830 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36940124 | TAATGTAAGTAGCTA[G/T]ACTGAATACTTTTTA | 15163 |
rs253029166 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36940843 | ATCTATACGCTGTTA[A/T]TGTAGATGAGCTTTA | 15163 |
rs253165233 | in-del | -/TTTTTTTT | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934576 | TTTTTCCACTAAGCC[-/TTTTTTTT]TTTTTTTTTTTTTTT | 15163 |
rs253188913 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36947077 | CATGTCTGCTGAGCA[C/T]GGTCTTAATTACTTT | 15163 |
rs253244781 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36947849 | CCTGTACAGCTCTCT[A/G]CCTTAGCCCCTTGGG | 15163 |
rs253393275 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Hcls1, Golgb1 | Mm_Celera | 16:36933403 | TTGCCTGTAATTCCA[A/G]CACTGAGGAGGCTGA | 15163 |
rs253480471 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36957140 | AGATCTCGCTCATTT[A/C]TACAAGTACCATTCC | 15163 |
rs253539184 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36958230 | CTGTCTCTGTGCCCT[C/T]TGGTTAGTCTGGCTA | 15163 |
rs253546566 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36950049 | GCCTGAGTTTGTAGA[C/T]GTGTTAACAGGCTGT | 15163 |
rs253564791 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36957805 | TAGACAGAAACTGTT[C/T]CATCTCCAAGGGAGA | 15163 |
rs253594121 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36940184 | TCTTTTTTCAGTATA[C/T]GTGTTTATGTACCAC | 15163 |
rs253603326 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36950573 | CTTAGAAACCCATAG[C/T]TACCGAGCAAATGGG | 15163 |
rs253836811 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36939611 | AACTTTGGTTATGAG[A/G]TCAGGCAAAACATTC | 15163 |
rs253849187 | snp | C/T | | | synonymous-codon | Hcls1 | Mm_Celera | 16:36962626 | CCCAGAGGGAAGCGA[C/T]GAGCTTTCCTTTGAT | 15163 |
rs253950395 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36958816 | CTTTTGTTTTAGGAT[A/G]AAATATCCTATAGAT | 15163 |
rs254223568 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36950152 | TAAGTAACAACAGGG[A/G]CCTGACTGGGTAAGA | 15163 |
rs254308862 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36950671 | CATACTGAGACCAGT[A/G]AAGTTCCGAGGGAGT | 15163 |
rs254323208 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36943159 | GTTGCACTTGTTCCG[A/T]GTCCTTGTCAGCACT | 15163 |
rs254343284 | in-del | -/AATAAATA | | | intron-variant | Hcls1 | Mm_Celera | 16:36946009 | ATGTTAATGCTTGAT[-/AATAAATA]AATAAATAAATAAAT | 15163 |
rs254396904 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36943673 | GCAATTGAGTTAAGG[C/T]TCTTCTTCTCTATGG | 15163 |
rs254488276 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36949959 | GCAGAGCTAGCACAC[A/G]GCACACAAAGCCAGA | 15163 |
rs254611312 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36956860 | GAGGATCAGAGACAC[A/G]CAGGGAAGAGAGAGG | 15163 |
rs254738095 | in-del | -/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36961791 | ATACATGCCCCTCCC[-/T]CCCCTCATACCTGGA | 15163 |
rs254861078 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36951275 | CTCCCTGCCTCCAGC[C/T]CCCCACTGGTTTGGC | 15163 |
rs254950781 | in-del | -/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36953698 | TTTGAAATATATTAA[-/G]GGGTTAGCACATGGT | 15163 |
rs255054135 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36954509 | TTAGAATTCCTGAGT[C/T]CTATAATTGAAAACA | 15163 |
rs255134841 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36939682 | CACCACAATACATGC[A/G]ACTGTTTCCAAAAGA | 15163 |
rs255160720 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36958106 | TCATCCAGATTTTCC[A/T]GTTGTATTGAATACA | 15163 |
rs255679403 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36951609 | GCTAGGCATGGTGGT[C/T]TTTACTCCTAGCATG | 15163 |
rs255691072 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36953379 | CCTTCCTCACTTTTT[C/T]ACCCACCCAACTTCA | 15163 |
rs255730854 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36949782 | GCTCCGTTGGAAGCA[C/T]GCTAGCACCTCATAA | 15163 |
rs255742336 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36941622 | AGGACAAATGCTTTT[A/G]TCTGCTGTTTTCCTA | 15163 |
rs255960434 | in-del | -/AA | | | intron-variant | Hcls1 | Mm_Celera | 16:36943828 | CACTACCACAGTGCT[-/AA]GTTATTATAGCTGTG | 15163 |
rs256472990 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36945338 | CCTCTCCTGTGACAC[A/G]GCCACTTTGCCTGGA | 15163 |
rs256518362 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36948695 | GTCTCTCCACCATAC[C/G]CCTTAAGTTATGTGG | 15163 |
rs256526046 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36946411 | AAAAGACAACAGACA[A/G]CAGGATGTTAGCTTC | 15163 |
rs256614283 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36950855 | CCCTCAATTTACTGT[C/T]GTGGTGGGTAAGATT | 15163 |
rs256685117 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Hcls1, Golgb1 | Mm_Celera | 16:36933258 | GGAGCCAAAGGAGAT[A/G]AGGTTCAGATTAGAA | 15163 |
rs256767654 | in-del | -/GTC | | | intron-variant | Hcls1 | Mm_Celera | 16:36950001 | CATGAACAGGCATGT[-/GTC]TAGAGAGGCAACATC | 15163 |
rs256770901 | snp | C/T | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934055 | GCAAAAGCAAGTTCT[C/T]AGTAGGATTATTTTT | 15163 |
rs256826445 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36947956 | TCTCTACCTTCTCAT[A/G]CTGGGATTAAAGGCA | 15163 |
rs256926234 | in-del | -/CCGGGT | | | cds-indel | Hcls1 | Mm_Celera | 16:36962113 | GACTATGAGCCAGAG[-/CCGGGT]CCAGAGACAGAGCCT | 15163 |
rs256950555 | in-del | -/TGATGATGATGATGATTGA | | | intron-variant | Hcls1 | Mm_Celera | 16:36949407 | CACTTGGATAAGAAG[-/TGATGATGATGATGATTGA]TGATGATGATGATGA | 15163 |
rs257438704 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36940684 | CCAGCTCTGTCATCA[C/T]TAGTGGTGTGAACTC | 15163 |
rs257557110 | in-del | -/CAG | | | intron-variant | Hcls1 | Mm_Celera | 16:36949720 | CAAATTACATCGCCT[-/CAG]CAACCCATGTGTTCT | 15163 |
rs257628295 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36955642 | CCTCAGGGAGGACTG[A/G]GAACTTTCTCCTGGG | 15163 |
rs257771928 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36943769 | CTGTATGGTTGACTT[C/T]TGGACTCTGTTCTGC | 15163 |
rs257958508 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36943653 | TTAATATTTATGTGC[A/G]GCATGCAATTGAGTT | 15163 |
rs258036408 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36961103 | CTACGGGTGCACATG[A/G]AAACCATATATATTT | 15163 |
rs258048454 | in-del | -/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36953792 | ACATAGAGTCAAGGA[-/G]GTATCTTGTGTAGTT | 15163 |
rs258093362 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36962444 | AGGTAAGTTTGAAGC[C/T]ACCTGAAGGGCCTGG | 15163 |
rs258184929 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36953389 | TTTTTTACCCACCCA[A/G]CTTCATGTTCTTTCT | 15163 |
rs258195850 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36949613 | AATGCCATGTAGAGC[A/T]TGTAAGGATCTATAA | 15163 |
rs258243743 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36946192 | GGTTTTCTATTATCT[A/G]TAATATTTTAATCAT | 15163 |
rs258396070 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36958928 | TGTTGACAGTGGGAT[A/G]TTGAATTTTCCCACT | 15163 |
rs258460948 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36950288 | GGCATGGAGTTTGCC[C/T]GGCCATGTGGGAACT | 15163 |
rs258470678 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36960944 | TCCCAGGCTGCTTCT[A/C]AGTTCCTGTGTCTTG | 15163 |
rs258552147 | snp | G/T | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36933853 | TATAAATAGCCTTAT[G/T]AGAACAAATAAAGTG | 15163 |
rs258787796 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36952077 | TATTATATCATCATT[C/T]AGGGTCTCTCATGTC | 15163 |
rs258847795 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36952875 | AACTGTATATGTGTT[A/G]GGGGCCTCCTATCAG | 15163 |
rs259009012 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36952135 | TGTATTTTTCTTTTT[A/T]AAAAATAAAAATAAA | 15163 |
rs259065280 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36944179 | CCTAAAGCATTTCAT[A/G]TTATGTTATGACTAT | 15163 |
rs259128034 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36943054 | TAATTGCTTATTCAT[A/G]CAGTCAGTGAGTGTT | 15163 |
rs259142301 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Hcls1, Golgb1 | Mm_Celera | 16:36933204 | CATCTCACTGGCCAG[C/T]ACCACATGGCTGTGA | 15163 |
rs259159402 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36961353 | GGATGTGTTGTACTG[C/G]ACTAGCAGAATGGAT | 15163 |
rs259367543 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36945193 | GCCAGCACTGGGATC[C/T]GGTTCATCTGATTCC | 15163 |
rs259385847 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36954701 | GGACAGATCCTAGGT[C/T]CTAATCCCTATTCCT | 15163 |
rs259397304 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36943441 | CAAGAGGAATGATTG[A/C]TCTTTTAATTTTCTG | 15163 |
rs259429638 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36946313 | TATGATTCTTGAGAC[A/G]GACCGCCTAATTGGT | 15163 |
rs259606850 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36951489 | TCTTTGTGAATAATA[C/T]AGAAACATTTTAGCG | 15163 |
rs259656065 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36944727 | TGGATTTTCAGTTGG[A/G]TGTGGCTACAGATAC | 15163 |
rs259712091 | in-del | -/GCTTAC | | | intron-variant | Hcls1 | Mm_Celera | 16:36945980 | CCCAGAAATTATCAG[-/GCTTAC]GTTGGAGAATGTTAA | 15163 |
rs259739319 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36954667 | ACCCCTCCCTCCCAC[G/T]CTTGTATAGAGTTGA | 15163 |
rs259805844 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36947458 | TGTATTCTGTCTGTA[C/T]TGCAACATCTCTTAT | 15163 |
rs259805884 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36955509 | CAACACTGATGGAAT[A/G]GACAGTGGGATTGGA | 15163 |
rs259838924 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36957816 | TGTTCCATCTCCAAG[A/G]GAGAATATGTATTGT | 15163 |
rs259975840 | in-del | -/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36955175 | TCCTTCCTTCAGACC[-/T]CTCTCTCTCTCTCTC | 15163 |
rs260116267 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36960743 | GCTGTTCCTTGGTTC[C/T]TGTGTCCTGACAGCT | 15163 |
rs260511032 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36941461 | GAGACTAGCTTAAGC[A/G]ATTCTACCCGTCTCT | 15163 |
rs260575390 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36942315 | TTTGAATTCAGCTCA[A/G]TCTGAATCTAAGGGC | 15163 |
rs260701235 | in-del | -/TGTTCCCT | | | intron-variant | Hcls1 | Mm_Celera | 16:36954579 | ATGTTACTTGCAAAA[-/TGTTCCCT]TGTTCCCTTGTCAAA | 15163 |
rs260752233 | in-del | -/TTTT | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934577 | TTTTTCCACTAAGCC[-/TTTT]TTTTTTTTTTTTGAT | 15163 |
rs260842683 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36957073 | CTCACTACCTCTGTG[C/T]CTTCCCCTCCACACG | 15163 |
rs261081878 | in-del | -/ATGGAATCCACC | | | intron-variant | Hcls1 | Mm_Celera | 16:36953503 | ACTTTCAAACAATTT[-/ATGGAATCCACC]ATGGAATCCACCTCA | 15163 |
rs261378751 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36949691 | CCTTATTGTTAGTTG[C/T]TACTTTACAAGCACA | 15163 |
rs261440378 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36956269 | TCTTAATCCTGTCTT[A/G]AGTCTCTCCTTGCTC | 15163 |
rs261603603 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36942443 | TGCCCCCTTTCCCTA[A/G]GATTGCTCTCCTCTT | 15163 |
rs261702735 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36955130 | CCTCTACCCGAGCCC[A/G]GAGCCCTTCCCTGGC | 15163 |
rs261737279 | snp | A/C | | | intron-variant | Hcls1 | Mm_Celera | 16:36947867 | TTAGCCCCTTGGGAC[A/C]GGCTTTCCCTCTGAG | 15163 |
rs261898505 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36948919 | TTAGCATAGGAGAGG[C/T]CCGGGTTCATCAGCA | 15163 |
rs262015508 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36954778 | ACATTCACCCACACA[C/T]ATACATAGCTCTGTC | 15163 |
rs262171017 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36940024 | TAAGAAGTGTCAGTG[A/G]TGACCACATTGCACC | 15163 |
rs262196543 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36946493 | CTGTCAACTGATACA[G/T]TCAGGGACTCAGAGT | 15163 |
rs262263574 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36939417 | GTCTGTGTTGGGGAC[A/G]TGGAAGAGAATGTAA | 15163 |
rs262296907 | in-del | -/TTTGCTCACTTGT | | | intron-variant | Hcls1 | Mm_Celera | 16:36948266 | CTGACATGCCCTAGC[-/TTTGCTCACTTGT]TTTGCTCCAGCCTGA | 15163 |
rs262414117 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36944530 | ACTTGCCACTCTGAA[A/T]GCTTCCCTGTATCCC | 15163 |
rs262680050 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36946985 | CTTGTGACGGTTAGT[A/T]TTAATTGTCACAATC | 15163 |
rs262746167 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36950372 | GGATTAGCCTGATCT[C/T]ATCCAGGACGGCTCT | 15163 |
rs262936809 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36944278 | ATGGCGACTCTGTAT[C/T]CTGAAAGCTTAGTGG | 15163 |
rs262956849 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36938345 | CATCAATTCTGGGTG[G/T]GGTCATACACACCTT | 15163 |
rs263006977 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36962559 | CCCTAAGGCTTAGAG[A/T]GGGCACAGAGGAATT | 15163 |
rs263136579 | in-del | -/GCTTGC | | | intron-variant | Hcls1 | Mm_Celera | 16:36948227 | GGAAAAACAGCAGTT[-/GCTTGC]GGTATCTAGCCAGTG | 15163 |
rs263337190 | snp | C/G | | | upstream-variant-2KB | Hcls1 | Mm_Celera | 16:36934154 | GAGCCATGCTTGGGA[C/G]GGGGGTGGGTGAGGA | 15163 |
rs263401055 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36953060 | TGGGACTCTCTTTAT[A/G]ATACAGGTAAATCAC | 15163 |
rs263432162 | snp | A/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36944070 | CAATCTATGAACCCG[A/T]GGCATTCCTCTACTT | 15163 |
rs263437289 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36952394 | GCTGGGATCAGAGGT[A/G]TGCACCACCACTGCC | 15163 |
rs263533736 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36941058 | TCACAAAAGCTTGTT[C/T]CATTCCTATTTGTTA | 15163 |
rs263653451 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36943373 | TTTATTGAGTTCCCT[A/G]TATAGTTTAGAAACA | 15163 |
rs263795465 | in-del | -/GTATGCCCTT | | | intron-variant | Hcls1 | Mm_Celera | 16:36935311 | GGACCCTGGGCCCTA[-/GTATGCCCTT]GATGATCTACACAGC | 15163 |
rs263814121 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36953205 | ATTGTTTGAAAGTGT[G/T]TGTATGTGTGTGTGT | 15163 |
rs263925968 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36962302 | GGGGCAGCAGAGAAA[C/G]GGGAGGAATCTCCCC | 15163 |
rs264156049 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36961025 | ACAGGCTTGTCAGCA[C/T]TCCTGGGAGACCAGC | 15163 |
rs264163559 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36951213 | AGAGCCTTGGCCACG[G/T]CTGGCCAGCTTCCCT | 15163 |
rs264298123 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36958439 | AAGCTGCTAGTGTAA[A/G]CGCTCTCCAGTTTCT | 15163 |
rs264465653 | snp | A/C | | | synonymous-codon | Hcls1 | Mm_Celera | 16:36957348 | GGTAAAGATGAGCCG[A/C]GAAGTCCAGCAGCCA | 15163 |
rs264595955 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36955569 | GGTACTGGGGAAGGA[A/G]TAACTAGGCCAGGTG | 15163 |
rs264630195 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36948431 | TTCCTGGTACCACTG[C/T]CAGAGGTACCAAGAA | 15163 |
rs264667060 | snp | C/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36949760 | CAGACTAAAGGGTGG[C/G]GACATAGCTCCGTTG | 15163 |
rs264702878 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36943217 | CCACTCTGTGGGTAT[A/G]CAGAGATGTTAATTT | 15163 |
rs264743217 | snp | A/G | | | synonymous-codon | Hcls1 | Mm_Celera | 16:36957387 | TGTGGAAGAGCCAGC[A/G]GCACCAGCCCAGTTG | 15163 |
rs264778110 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36953771 | TGCGCGCGCGCGCGT[C/T]CTATGCACATAGAGT | 15163 |
rs264938352 | in-del | -/A | | | intron-variant | Hcls1 | Mm_Celera | 16:36949889 | ATTTGCCCGTCAAAT[-/A]AAAGAATCACAGGAT | 15163 |
rs264997940 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36947284 | ACCCTAACCTGGAAT[A/G]GTAGCCAAATAAAAC | 15163 |
rs264999389 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36936892 | CAGTCTTCCACAGAC[A/G]GGGAGCATTTTCAAT | 15163 |
rs265250641 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36951906 | CTTAGCTATTCTTCA[C/T]ATTTTCTCATTTCTT | 15163 |
rs265366742 | in-del | -/TCTC | | | intron-variant | Hcls1 | Mm_Celera | 16:36955815 | TCTTCCCATCATCCA[-/TCTC]TCTCTCTCTCTCTGA | 15163 |
rs265375219 | snp | G/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36952829 | GGGTTAGATTCATCA[G/T]CTCTGAATGAACACA | 15163 |
rs265378481 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36945046 | AGCCATTCAGAAGCT[C/T]CGGGCGCCCGCCCGC | 15163 |
rs265592970 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36935378 | TGCTAACCTGAAGGC[A/G]ACCCACGGAAGATGA | 15163 |
rs265678062 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36949068 | GGGCTGCAACACTTC[A/G]AGAAGGTGAAGGGTA | 15163 |
rs265691753 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36940239 | AGATGCTCTGGAGCT[A/G]GAGTTACAGATTGTT | 15163 |
rs265727260 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36942569 | CCTTAATACAGCTTA[C/T]TTTAAAAACTCAGTG | 15163 |
rs265763370 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B | Hcls1, Golgb1 | Mm_Celera | 16:36933160 | GGATGGAGGAGTGGC[A/T]ACTGGAGGAGAAAGT | 15163 |
rs265767857 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36950174 | TGGGTAAGACCCTGC[C/T]GGGGACCTTTGAAAT | 15163 |
rs265872418 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36960237 | TTGTTTCTATTTCCA[C/T]TTTTAGTTCCTGGAA | 15163 |
rs266063638 | snp | A/G | | | intron-variant | Hcls1 | Mm_Celera | 16:36939560 | TTACATTGTTCTCTT[A/G]AAGCAGGTTTAACAT | 15163 |
rs266157409 | snp | C/T | | | intron-variant | Hcls1 | Mm_Celera | 16:36956706 | TGGCTTCCTCTCCTC[C/T]CAGACTATGCCTTGT | 15163 |
rs578467111 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36946435 | TAGCTTCTCGAGAGC[A/G]TAAATCAGGCTACAT | 15163 |
rs578544483 | snp | A/C | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36946037 | ATAAATAAATAAATA[A/C]ATAAATACACAAATA | 15163 |
rs578572586 | snp | G/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36959961 | TGGCCCTTTAAGTTG[G/T]GAATCTTCACTCTCT | 15163 |
rs578800162 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36940775 | CTGGATTGAATAGTA[C/T]ATGTGACTGACTGTC | 15163 |
rs578823911 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36952976 | TGGTCCTCCTACAGG[A/G]TCACCCTTCTCCTCA | 15163 |
rs579019898 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36939829 | TTGGTTCTGGGTAGC[C/T]CCAGGCTGCCATATT | 15163 |
rs579041891 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36957497 | CCAAGTGATAGGCAT[A/G]GATAGATAGATAGAT | 15163 |
rs579173742 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36954668 | CCCCTCCCTCCCACT[C/T]TTGTATAGAGTTGAT | 15163 |
rs579411530 | snp | C/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36959750 | TGCCTTTATATGTTA[C/G]TTGACCTTTTTCCCT | 15163 |
rs579481286 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36951726 | CAAAAATCCAAATGA[A/G]ACAAAGCAAAGCCAT | 15163 |
rs579510025 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36960464 | GTGTGTTGGAGTATC[C/T]AGGGTTCACTGTGTT | 15163 |
rs579570605 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36943334 | GTTCATATATTTACT[C/T]AGTTTTAATGTACTT | 15163 |
rs579751628 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36949715 | AAGCACAAATTACAT[C/T]GCCTCAGCAACCCAT | 15163 |
rs579972135 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36957656 | CTCTTAAATATACAT[A/G]ATATCTTCTGAAGCT | 15163 |
rs580027991 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36944012 | ACTGGAGTTGTTAGA[C/T]CATTTAGAGGGATAG | 15163 |
rs580119976 | snp | A/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36943704 | ATATCCAATTTCCAA[A/T]CACAATCCAAACTCT | 15163 |
rs580418831 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36957960 | TAAACCCATCTGGTC[C/T]TGGGCTTTTTTTGTT | 15163 |
rs580508563 | snp | A/G | | | upstream-variant-2KB | Hcls1 | GRCm38.p3 | 16:36933698 | CTGTTCTGCTCAGGG[A/G]TGAACATGGGGTGTT | 15163 |
rs580596589 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36948288 | ACTTGTTTTGCTCCA[A/G]CCTGATCCTGTCTGA | 15163 |
rs580631428 | snp | A/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36954569 | TAGAACTCCAAATGT[A/T]ACTTGCAAAATGTTC | 15163 |
rs580723191 | snp | C/T | | | upstream-variant-2KB | Hcls1 | GRCm38.p3 | 16:36934455 | TTTCTCCCTCCACGT[C/T]CTGCCTTCTCCCTTC | 15163 |
rs580956963 | snp | A/C | | | upstream-variant-2KB | Hcls1 | GRCm38.p3 | 16:36933891 | TCTAGAATCAATCCC[A/C]TGGGAAGTGACTTTA | 15163 |
rs581021957 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36959233 | TGTCTTTGACACTGA[A/G]GTGCATTTCCTCTAT | 15163 |
rs581185996 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36958678 | CCAGCCTTAGTCCGT[A/G]GTGATCTGATAGGAT | 15163 |
rs581390632 | snp | A/C | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36946025 | ATAAATAAATAAATA[A/C]ATAAATAAATAAATA | 15163 |
rs581506302 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36945974 | GTTATTCCCAGAAAT[C/T]ATCAGGCTTACGTTG | 15163 |
rs581523043 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36937965 | CAGGGGTGCAGAAAG[A/G]AAACAGCCATGGCTG | 15163 |
rs581581381 | snp | G/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36959634 | TGGGTATAGTAGCCT[G/T]GGCTGGAATTTGTGT | 15163 |
rs581878798 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36941477 | ATTCTACCCGTCTCT[C/T]ATCAGTGTATAGAGA | 15163 |
rs581978368 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36946844 | GTCCATTTGGGCTTT[A/G]ATGCAGAATGCCTTT | 15163 |
rs582090610 | snp | A/C | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36946041 | ATAAATAAATAAATA[A/C]ATACACAAATACTAG | 15163 |
rs582325290 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36960181 | TGATCTCTTTCCTAG[A/G]TTTTCTATCTTCAGA | 15163 |
rs582328084 | snp | A/C | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36959832 | TATGTGACAGGAAGA[A/C]TTTCTTTTCTGGTCC | 15163 |
rs582551029 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36949681 | GGTCCTCTTCCCTTA[C/T]TGTTAGTTGCTACTT | 15163 |
rs582585981 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36957534 | ATAGATAGGGCAGAT[A/G]CATTTCTTTTTTCCT | 15163 |
rs582887321 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36955022 | AGATGATCTCTCACG[A/G]GCTCTATACATAGCC | 15163 |
rs582945747 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36944461 | CTCCGTCAATACAAG[C/T]CATGTGAAAAACGTG | 15163 |
rs583014167 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36957867 | ATTTGGGTTGTGTTC[C/T]TTCCATTTCTATTTT | 15163 |
rs583193578 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36951841 | TAACAAAGAATATAT[A/G]TATATATATATACCA | 15163 |
rs583246800 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36961783 | TTGCTTTCCATACAT[A/G]CCCCTCCCCCCCTCA | 15163 |
rs583250418 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36951064 | CCTAAAACTGAGATG[A/G]AAGTAAGGCTAACTG | 15163 |
rs583529163 | snp | A/G | | | upstream-variant-2KB | Hcls1 | GRCm38.p3 | 16:36934153 | GGAGCCATGCTTGGG[A/G]CGGGGGTGGGTGAGG | 15163 |
rs583532980 | snp | A/G | | | upstream-variant-2KB | Hcls1 | GRCm38.p3 | 16:36933873 | CAAATAAAGTGCTCC[A/G]AGTCTAGAATCAATC | 15163 |
rs583786266 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36958715 | GATAATTTCAATCTT[C/T]TTGTATCTGTTGAGG | 15163 |
rs583872680 | snp | C/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36943974 | GAAAAAAAAATGCCT[C/G]TTGAGAGTTTGACTG | 15163 |
rs584107351 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36958509 | GCTTTCACTGTGTCC[C/T]ATAAGTTTAGGTATG | 15163 |
rs584144303 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36946225 | GACATTAAGCTTTGC[C/T]GTATTTAAAGTTATT | 15163 |
rs584153082 | snp | A/C | | | upstream-variant-2KB | Hcls1 | GRCm38.p3 | 16:36934465 | CACGTTCTGCCTTCT[A/C]CCTTCCTCGTGAGTT | 15163 |
rs584237565 | snp | C/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36959245 | TGAAGTGCATTTCCT[C/G]TATGCAGCAAAATGC | 15163 |
rs584256127 | snp | G/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36952634 | TTTCTTTTCTTTTCA[G/T]GTGAACATTCTATTT | 15163 |
rs584490130 | snp | C/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36954571 | GAACTCCAAATGTTA[C/G]TTGCAAAATGTTCCC | 15163 |
rs584580356 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36940688 | CTCTGTCATCATTAG[C/T]GGTGTGAACTCAGTC | 15163 |
rs584720446 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36939228 | GAAAGAATGATGGAT[A/G]CTTAGCAGAACTATC | 15163 |
rs584807313 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36952484 | TCTGTTCTTAAAATA[C/T]ATGGTTTTGACTCTA | 15163 |
rs584810366 | snp | A/C | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36946017 | GCTTGATAATAAATA[A/C]ATAAATAAATAAATA | 15163 |
rs585050569 | snp | A/C | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36946033 | ATAAATAAATAAATA[A/C]ATAAATAAATACACA | 15163 |
rs585157387 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36942475 | AAAGCCGCTGAGTAT[A/G]TTTAGTCCGGCTTTA | 15163 |
rs585196809 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36959697 | TCTTCTAGCTTTCAT[A/G]GCCTCTGGTGAGAAG | 15163 |
rs585387894 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36957652 | ATGCCTCTTAAATAT[A/G]CATGATATCTTCTGA | 15163 |
rs585416445 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36960340 | TTTAAGGGCTTCTAG[C/T]TGTTTACCTGTGTTC | 15163 |
rs585526767 | snp | A/C | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36957870 | TGGGTTGTGTTCCTT[A/C]CATTTCTATTTTGTG | 15163 |
rs585948670 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36943335 | TTCATATATTTACTC[A/G]GTTTTAATGTACTTA | 15163 |
rs585955929 | snp | A/C | | | missense | Hcls1 | GRCm38.p3 | 16:36962120 | GAGCCAGAGCCAGAG[A/C]CAGAGCCTGACTATG | 15163 |
rs586041931 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36959934 | TTCTATAATTTTGTT[A/G]AAGATATCTACTGGC | 15163 |
rs586064183 | snp | A/C | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36955771 | CCTTTTTTTCTCTCC[A/C]AACCCCCATACCCTG | 15163 |
rs586171471 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36949704 | TGCTACTTTACAAGC[A/G]CAAATTACATCGCCT | 15163 |
rs586288584 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36945077 | CCCGCCCCGCCCCGT[C/T]CTTTTCAGACCCTGG | 15163 |
rs586406608 | snp | C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36947755 | TGTATATGGTGCATA[C/T]ATATATGCACGTGTG | 15163 |
rs586543989 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36959112 | TTTTTGATAACTTTT[A/G]ATTGAAAGTTGATTT | 15163 |
rs586559415 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36951523 | TTCTTTCTACCATCT[A/G]TATTACTGTTATATA | 15163 |
rs586845115 | snp | C/T | | | upstream-variant-2KB | Hcls1 | GRCm38.p3 | 16:36933876 | ATAAAGTGCTCCAAG[C/T]CTAGAATCAATCCCC | 15163 |
rs587034665 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36944011 | CACTGGAGTTGTTAG[A/G]CCATTTAGAGGGATA | 15163 |
rs587147348 | snp | A/C | | | upstream-variant-2KB | Hcls1 | GRCm38.p3 | 16:36934396 | TAGTCAGAACTCTGT[A/C]AGTGAGCTCAGACTC | 15163 |
rs587255183 | snp | A/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36952633 | TTTTCTTTTCTTTTC[A/T]TGTGAACATTCTATT | 15163 |
rs587488483 | snp | A/G | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36958529 | GTTTAGGTATGTTGT[A/G]CCTTCATTTTCATTA | 15163 |
rs587496463 | snp | A/C | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36946021 | GATAATAAATAAATA[A/C]ATAAATAAATAAATA | 15163 |
rs864279793 | snp | C/T | | | utr-variant-3-prime | Hcls1 | GRCm38.p3 | 16:36962915 | TAGAATCGCTCCAGG[C/T]GGGGGTGGGGGTGGG | 15163 |
rs864303084 | in-del | -/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36954538 | AAAATTACATTCCCC[-/T]AATTGAACACAGGGC | 15163 |
rs864306742 | snp | A/C/T | | | intron-variant | Hcls1 | GRCm38.p3 | 16:36946029 | ATAAATAAATAAATA[A/C/T]ATAAATAAATAAATA | 15163 |