SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3724626 | snp | A/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Six4, Mnat1 | Mm_Celera | 12:73110255 | GTGGCCTTGTCACTA[A/T]CAGACTCCTGCCCTG | 17420 |
rs3725726 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Six4, Mnat1 | Mm_Celera | 12:73110400 | AAGCAGTTTGGAAGC[C/T]TGGTGAGACTTGGTC | 17420 |
rs6210064 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73149393 | tttcaatgctatctg[A/G]gcagcttggttaaat | 17420 |
rs6210156 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73149441 | AGTAAAAGCTGAGGG[A/C]TGGTGGGATTGCTCA | 17420 |
rs6210653 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73149513 | tgatctcagaagcct[C/T]atggtggaagcagag | 17420 |
rs6224615 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73149781 | acacacacatacatg[A/G]atatgcacacataca | 17420 |
rs6225653 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73149956 | AAAAGGGCTCTATAT[A/C]TTATGGTATGTTTTT | 17420 |
rs6260915 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73185223 | TCTAGAGACATGCTT[A/G]TCACCACAACCCATG | 17420 |
rs6278611 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | GRCm38.p3 | 12:73186186 | tcaaactcaggtacc[C/T]gggcctttgggcaag | 17420 |
rs6279595 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Mnat1 | Mm_Celera | 12:73186393 | ACTTGTTGCAGACAC[A/G]CACAGCAATGCAGTG | 17420 |
rs6308785 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73193731 | AGTAGAGCATTATGG[A/G]AATGCAAGCACAAAT | 17420 |
rs6309780 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Mnat1 | Mm_Celera | 12:73193877 | AATTATGTGTCTGTT[A/G]CTACTATTTCCAGTT | 17420 |
rs6309869 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Mnat1 | Mm_Celera | 12:73193940 | GACAGTCTAAGTAGA[C/G]GACACAGAGCTCATC | 17420 |
rs6310323 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73193996 | TCCCACCTGCTACCT[A/G]TAGCAACCTGAGTAT | 17420 |
rs6311516 | snp | G/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73194261 | cagaagagggagtca[G/T]atctcattacngatg | 17420 |
rs6311535 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73194272 | gtcanatctcattac[A/G]gatggttgtgaccca | 17420 |
rs6312539 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Mnat1 | Mm_Celera | 12:73194427 | AAGGATGATGACAAA[C/T]AAGCAACATTGAAAA | 17420 |
rs6344555 | snp | A/T | 0.444444 | 0.157135 | downstream-variant-500B, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73274272 | CGTCTCCCGTGTTCT[A/T]GCAGATAGAGGTGTC | 17420 |
rs6345120 | snp | C/T | 0.5 | 0 | downstream-variant-500B, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73274365 | GCCAGGAGTTAAACT[C/T]CAGTGCCAAGGCTCC | 17420 |
rs6356996 | snp | G/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73208948 | TATGTTTGTTTGTTT[G/T]TTGTTTTTTGTTTTG | 17420 |
rs6357488 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73209053 | CTGTACAAGTTGTCA[C/T]CATCACTGGCCAACT | 17420 |
rs6357519 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Mnat1 | Mm_Celera | 12:73209069 | CATCACTGGCCAACT[A/G]TGAGTTCANTTCTGG | 17420 |
rs6357912 | snp | C/G | 0.207612 | 0.24638 | intron-variant | Mnat1 | Mm_Celera | 12:73209078 | CCAACTNTGAGTTCA[C/G]TTCTGGTGTCACAAT | 17420 |
rs6394401 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73139151 | AACTCAAGTTGtctc[C/T]ccttcccctctcttt | 17420 |
rs6394962 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73139256 | ccaccccTGCTGGGT[C/T]AGGATGGGATCCATT | 17420 |
rs6395389 | snp | A/G/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73139288 | CCACATGCATATTAG[A/G/T]CTAGCACTGTNTTAC | 17420 |
rs6395411 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73139299 | TTAGNCTAGCACTGT[A/G]TTACTGACTTAATGT | 17420 |
rs29122859 | snp | A/C | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73118447 | GTACTTGCTGAAGTA[A/C]TTATGTTTCTGGGTT | 17420 |
rs29124329 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73257120 | TTAGCAGTGGCAGCT[C/T]GATCCACTCACAAAA | 17420 |
rs29124673 | snp | G/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73224985 | CGACTGAAGATAGTA[G/T]GCGACTGTCTTAGCC | 17420 |
rs29125002 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73161127 | TGTATTTATTTATTT[A/G]TTTATTGTTTTGTTT | 17420 |
rs29125443 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73191541 | GTTGCCTGGAAGTCC[A/G]TCTTCCACTAGCAGC | 17420 |
rs29125984 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73205030 | GTGAATATTTCAGGT[A/G]AATAATAATTTTCTT | 17420 |
rs29126515 | snp | A/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73161135 | TTATTTGTTTATTGT[A/T]TTGTTTTGTTTTTGT | 17420 |
rs29126694 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73224929 | AGGGCATACAGGGAG[C/T]CCCATCCTGTATCTC | 17420 |
rs29127160 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73125020 | GACAGCGTAACTGTG[A/T]CTGGATGGTTTAAGA | 17420 |
rs29127163 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Mnat1 | Mm_Celera | 12:73195387 | TTCACTGGGAAGATG[C/T]GCCATTTTATTTTAA | 17420 |
rs29127193 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73124960 | TCTTTTTTTTTTTTT[C/T]CCACGACAGGGTCTC | 17420 |
rs29127491 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73219247 | CCTAAGTTAAGTTTT[A/G]GTCAGTGTATCGACT | 17420 |
rs29128187 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73205568 | CAAAATAATTTAATA[G/T]TAAATTATTTAAAAA | 17420 |
rs29128309 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73138090 | AGGTGCTCTTACCCA[C/T]TGAGCCATCTCACCA | 17420 |
rs29129575 | snp | A/G | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73153512 | GACAATTTAATTAAT[A/G]TAATAGGAGTTCATT | 17420 |
rs29129832 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73230663 | CTAATATTTTTTCTG[C/T]TCCAGGTTCTTTTCG | 17420 |
rs29130119 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73144980 | TCCTACAACATTCAT[A/G]CCCCACTCTTTCATA | 17420 |
rs29130443 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73173521 | CATATAACAATAAAT[A/G]AATCTTAAAAAATAA | 17420 |
rs29130541 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73218956 | GCGGAGCCATCTCTC[A/G]AAAATTACTACAAAT | 17420 |
rs29130576 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73177129 | TGGCCGAGTTATAGG[C/T]CAGCCTGGATTGCAA | 17420 |
rs29130607 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73260337 | CCTCTACTCTCCTAA[C/T]CCTTCCATATCCACC | 17420 |
rs29131232 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73132706 | GGTGAGTACTTAGGA[A/G]ACTGACTAGGTTATG | 17420 |
rs29131425 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | GRCm38.p3 | 12:73166367 | TGCATGGGAAATGAA[A/C/T]AAAGCAGATTTTTAA | 17420 |
rs29132000 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Mnat1 | Mm_Celera | 12:73226524 | CACTTTCCACTGTCA[C/T]TGGACTGTAACTGAC | 17420 |
rs29132084 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | GRCm38.p3 | 12:73154731 | TGTGTGAGAGAGAGT[G/T]TGTGTGAGTGTGTGA | 17420 |
rs29132984 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Mnat1 | Mm_Celera | 12:73205837 | TTTTGCTAGATCAAT[G/T]ATCAAGTGTGGTAAT | 17420 |
rs29133176 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Mnat1 | Mm_Celera | 12:73198900 | ATAACAGCACATGTT[A/G]ATGAGGTGTGTCTGT | 17420 |
rs29133196 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73153995 | AAATTTTAGGGCAAG[C/T]CTGGGCTACATAGTG | 17420 |
rs29133522 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Mnat1 | GRCm38.p3 | 12:73218515 | TAAAACAAAACAAAA[A/C]ACCGATTACCAAATA | 17420 |
rs29133562 | snp | A/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73128854 | GTTTTTTGTTTTTTT[A/T]AATTTAACTAAGTTG | 17420 |
rs29133755 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Mnat1 | Mm_Celera | 12:73236171 | TTTGTTATGTAAATA[A/C]ATTTTGTAAACTTAA | 17420 |
rs29133844 | snp | A/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73233970 | TCTCTGGGCTGGTAG[A/T]CTTGGGTTCTATAAG | 17420 |
rs29134002 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73219890 | ATGGATAATATTCTA[C/T]ATATGATTACTGAGG | 17420 |
rs29134072 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73169511 | CCTCTTAGTTCTTAT[A/T]TTTGGGGGTATACAT | 17420 |
rs29134475 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73176446 | TTGCCCTTTGTACTC[C/T]ACATCCATGCACACA | 17420 |
rs29134794 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73273675 | CTTCCTTGCTAGAAG[C/T]CACACTTCTCATCTT | 17420 |
rs29134892 | snp | C/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73199117 | TGTTGCTAGTGAGAA[C/G]AGGAAATGCTAGTGA | 17420 |
rs29134910 | snp | C/T | 0.265928 | 0.249492 | utr-variant-3-prime, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73272624 | GTTCCAGCCCCGCAG[C/T]TGCACAGCACACCAC | 17420 |
rs29135350 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Mnat1 | Mm_Celera | 12:73224142 | ATGCTCACGAGACTG[C/T]AGGTCACTGAGGAAA | 17420 |
rs29135729 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73227152 | CAATTAATTGTTCAC[C/T]TTATATGGTTTTCTT | 17420 |
rs29136183 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73256930 | CCTCCCGAGTGCTGG[A/G]ATCAAAGGTGTGCAC | 17420 |
rs29136912 | snp | A/C | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73146362 | TTGAAGGAAGTAAGC[A/C]TTCTAGTTAGATATG | 17420 |
rs29136996 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73272312 | TGAACATTTCAATCT[C/T]GGAATTCCTTTCCAA | 17420 |
rs29137025 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73143231 | AAATATCAACCCTTT[C/T]CCCCTTGAGTTGCAT | 17420 |
rs29137321 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Mnat1 | Mm_Celera | 12:73203065 | GGCTAGATAGCTTCT[C/T]CACAATGGCAGCTTT | 17420 |
rs29137513 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73179750 | AGGCTCATAGACTCT[C/T]CCGGCTGCCTCTTCT | 17420 |
rs29137606 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73125815 | AATTAGTAAGTGGTG[G/T]TTATTTATTTTGAGT | 17420 |
rs29137880 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73200152 | TTCACTAAGTACAAG[A/G]TATAGGGGGAAGGCA | 17420 |
rs29138837 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73144108 | CCTCCCCCCAGGGGG[A/G]AAAAATCTCATGAAA | 17420 |
rs29139167 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | GRCm38.p3 | 12:73139636 | GTTTTTGTGACAGGG[G/T]TTGTCTGTGTAGCCC | 17420 |
rs29139427 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73156699 | GAGGTCCCATTTATC[A/G]ATTCTTGATTTTACA | 17420 |
rs29139535 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Mnat1 | Mm_Celera | 12:73200788 | CACAGTCACATTGTG[C/T]GGGTTCAGATTCTGG | 17420 |
rs29139693 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73251233 | GTATGAGTGGGTGTC[C/T]AACCCACACCTTGCT | 17420 |
rs29140112 | snp | A/G | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73199274 | ATAAAGCCGGTCGCC[A/G]CCAGGTGTAAGACTT | 17420 |
rs29140324 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Mnat1 | Mm_Celera | 12:73230243 | GGTTTTATAGTAAGT[C/G]TGAATATGACAGCAG | 17420 |
rs29140442 | snp | A/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73198061 | CTTTTTTTCTAGATT[A/T]AAAAAAAAAGATTTA | 17420 |
rs29140477 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73239736 | AGACCTCAAAGCCCC[A/C]CCACCACAGTGATGC | 17420 |
rs29140969 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73166155 | ATCAGTATATAGCTC[C/T]CAGCTATTTCTCCAG | 17420 |
rs29141284 | snp | A/C/G | 0.375 | 0.216506 | intron-variant | Mnat1 | GRCm38.p3 | 12:73208307 | AGCACCTGCATGGTG[A/C/G]CTTGTTACAAACTCC | 17420 |
rs29141355 | snp | A/C | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73154884 | TTTCTGACTCAACTA[A/C]TGCAGCTAGCTAGCT | 17420 |
rs29141392 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73257177 | TTGGAATAGCAAACA[C/T]GAATCAGCAGCAGTG | 17420 |
rs29141465 | snp | G/T | 0.265928 | 0.249492 | intron-variant | Mnat1 | Mm_Celera | 12:73230513 | GCAGCTTTGGAGTTT[G/T]AAAGTTAATATTGAG | 17420 |
rs29141925 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Mnat1 | Mm_Celera | 12:73223602 | TATACTTTGGTAAAG[A/G]GCTTTGCCTGTTGAA | 17420 |
rs29142984 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73229503 | GGTCCAGTGACCTCA[C/T]TCATTGGCACTTGTT | 17420 |
rs29143209 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Mnat1 | Mm_Celera | 12:73200221 | TGTTTTATTTTAGCA[C/G]TGTGTCTCTTGTGTC | 17420 |
rs29143446 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73209595 | GCCACCCCTAACCTT[C/T]CACTCCTAAATAAGT | 17420 |
rs29143952 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73198126 | CACTCCAGAAGAGGG[C/T]GTCAGATCTCATTAT | 17420 |
rs29144096 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73261686 | ATTTTTATAGTTTCC[A/G]TTGTTATATCTCCCT | 17420 |
rs29144501 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73160971 | ATTAGTCTTTTTTTT[A/C/T]AACATGATTTAAAGT | 17420 |
rs29144696 | snp | C/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73217574 | ACCCTTCAGGTACAG[C/G]TGGTGCCCGCACCTC | 17420 |
rs29145160 | snp | C/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73186443 | TATGAAAGGAAGGCA[C/G]TGAAGACTAGTCTTA | 17420 |
rs29146099 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Mnat1 | Mm_Celera | 12:73236321 | GCTAGAGTTTACGTC[C/T]TGACTCATAGCACTA | 17420 |
rs29146405 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73126034 | GCACTTGAGGCCATG[C/T]GCAGCTTTTTGTGTG | 17420 |
rs29146648 | snp | G/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73152962 | CTGTTTAGTTTTTTG[G/T]TTTTGTTTTTGTTTT | 17420 |
rs29146653 | snp | A/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73134872 | CTGAGGTGTGACTTT[A/T]AAAAAATTACAAATT | 17420 |
rs29146785 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Mnat1 | Mm_Celera | 12:73187775 | AGGTGAAATCTAATG[A/G]GAACCATTTCAAATG | 17420 |
rs29146966 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Mnat1 | Mm_Celera | 12:73158480 | CCACTTTTTTATTTT[C/G]AAGGATTCACACGAA | 17420 |
rs29147469 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73169693 | TCACAGATACATTAC[A/C]CCCCCCCCCCCCTTG | 17420 |
rs29147582 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73190977 | TCACCTAACCCATGG[C/T]GGCTTCTCCCTCTCG | 17420 |
rs29148497 | snp | C/G | 0.375 | 0.216506 | utr-variant-3-prime, downstream-variant-500B, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73272879 | GATTTTTTTTTCTTC[C/G]TCCTCCTCCTTGTGT | 17420 |
rs29149277 | snp | A/C | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73136052 | CTGGTTTTGTTGATT[A/C]TTTGTGTAGTTCTTT | 17420 |
rs29149410 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73172059 | CAAGCAGAACAGCCA[C/T]GACAAAGAAAGTTTC | 17420 |
rs29150348 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73182619 | TCTGTCCCTCTGTGG[A/G]TCGATGATGGCCACT | 17420 |
rs29151032 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73241056 | ACCTTGAGAACCTCC[A/G]GTCTATCATGTGGGT | 17420 |
rs29151185 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73175341 | ATCCTATACATATAT[C/T]CAGTTATTCTTTGTT | 17420 |
rs29151946 | snp | C/G | 0.387812 | 0.208586 | utr-variant-3-prime, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73273851 | TAATTGGTAGTTCAC[C/G]CTTCTGTATTCAATC | 17420 |
rs29152293 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73135204 | TGAATTAGATAGTGT[C/T]CCTTCTGTTTCTTTT | 17420 |
rs29153122 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Mnat1 | GRCm38.p3 | 12:73227659 | TAAATTAAAATTTGT[C/T]TTAAATAGCAAATAA | 17420 |
rs29153447 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73204272 | GCTCTGTCTCTCTCT[C/G]TTTTGCTCTCTGTCT | 17420 |
rs29153500 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | GRCm38.p3 | 12:73200699 | TCTCATTTTTTTTTT[A/T]AGTCGGATAGTACAA | 17420 |
rs29153843 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73208110 | AGGTGATTCATGCTA[C/T]ATTATAGCTTCACAG | 17420 |
rs29154451 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73224957 | CTCAGGACTTGGCAA[C/T]CTGCAATACTGACGA | 17420 |
rs29154615 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Mnat1 | Mm_Celera | 12:73145654 | TGGGGTTCTTTTAGT[C/T]CCTGCCTTCTTCTGC | 17420 |
rs29154620 | snp | G/T | 0.33241 | 0.236027 | intron-variant | Mnat1 | Mm_Celera | 12:73120261 | GTTTCAAGCCATTTG[G/T]TGACAGTGAGCTTCT | 17420 |
rs29155448 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73147975 | TAACACTCATACAGA[C/T]ACATGCACACACACA | 17420 |
rs29155830 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Mnat1 | Mm_Celera | 12:73190043 | TGAATTGGTTTTAGT[A/G]TCTAATTATAAGATT | 17420 |
rs29155950 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73203046 | TGAATTTTCTGGAAC[A/G]GAAGGCTAGATAGCT | 17420 |
rs29156141 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Mnat1 | Mm_Celera | 12:73200242 | CTCTTGTGTCGAACA[G/T]GTTAAGCATGAGAGA | 17420 |
rs29156569 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73125846 | AATATATAGAGATGT[A/G]CACATTAGGAAACAG | 17420 |
rs29157975 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73170847 | TTAAATCACAGTAAC[A/G]GGCATTCTTGAATTT | 17420 |
rs29158518 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Mnat1 | Mm_Celera | 12:73206488 | GCAAAGCGCACAACT[A/G]CTTTGTAGAGGTCAC | 17420 |
rs29158820 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Mnat1 | Mm_Celera | 12:73126702 | TTTTGGGGCCTGCAA[C/T]ATGGTTAGCTTGAGT | 17420 |
rs29159120 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73252678 | TTTAAAGACATGATG[C/T]CATTTAGCTCAGGCT | 17420 |
rs29159399 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73156124 | TTCTTTCCAACTTCT[A/G]GCTATTATAAACAAG | 17420 |
rs29159930 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73176862 | TTAGCCCTCTTGTAT[A/G]TGGAGAACAAGCACA | 17420 |
rs29159983 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73132818 | ATTTTCTCTTCTGCA[A/G]GAATATCCAGTTGAC | 17420 |
rs29161372 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73213801 | TGGTCCAGTCTATTT[A/G]GAGTTCTGTAGGCTT | 17420 |
rs29161497 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269634 | AGTAAAAGTTTTGTG[C/T]AGTTCTGGAGATCAA | 17420 |
rs29161600 | snp | A/T | 0.465374 | 0.126941 | intron-variant | Mnat1 | Mm_Celera | 12:73206517 | ACAGTGGTCACAGGC[A/T]TGTGCAACAGAGTCA | 17420 |
rs29161830 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Mnat1 | Mm_Celera | 12:73207343 | TAGGTTTTTCATTGC[C/T]CTTAGGTTACTGTTT | 17420 |
rs29161891 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73153031 | GGCTGTCCTGGAACT[C/T]ACTCTGTATACCAGG | 17420 |
rs29162320 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Mnat1 | Mm_Celera | 12:73208007 | TACATAAATAAGAAC[C/T]TTATACTTTATAATT | 17420 |
rs29162378 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73257206 | TGGCACTACCTAGCA[A/G]TGACAGCCGGCCTCA | 17420 |
rs29163800 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Mnat1 | Mm_Celera | 12:73195398 | GATGCGCCATTTTAT[G/T]TTAAGGGTCTTGAAT | 17420 |
rs29163968 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73225815 | GGGATTAAAGGCGTG[C/T]GCTACCATGCCTGGC | 17420 |
rs29164741 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Mnat1 | Mm_Celera | 12:73227526 | TCTTCATTTTGGGGG[A/G]TTTTGTAGTATTGCG | 17420 |
rs29164889 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73199382 | AATGAATACTGAATG[A/G]TAATATTAATACTAG | 17420 |
rs29165063 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73186522 | GGATTTATTTTATGA[A/G]TAAAATTGAGTCCTT | 17420 |
rs29166328 | snp | G/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73234728 | TTGGCGGTGTGTGTG[G/T]GGGGTACTTTAAGTT | 17420 |
rs29166511 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73136390 | CCATGTGTATGTGTG[C/T]TTTCTGTTGTTTTTG | 17420 |
rs29167154 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73202478 | AAATAATCCTTAGTC[C/T]GTTTTAAAAAGAACT | 17420 |
rs29167802 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Mnat1 | Mm_Celera | 12:73256308 | TCACCTGGCCAGACT[A/G]TGGCAAAGGATATGC | 17420 |
rs29167940 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Mnat1 | Mm_Celera | 12:73209564 | CACTCTTCCCTGAAT[A/G]CACAGCCTACAGGTA | 17420 |
rs29168016 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Mnat1 | Mm_Celera | 12:73161985 | TTGAGTATAATGTTT[C/T]TTATTTTAGTTCTCT | 17420 |
rs29168283 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73239213 | AGTTGTATCTTGGGT[A/G]TTCTAGGTATGGATA | 17420 |
rs29168284 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73260215 | TTGCTAACCAAAGCC[C/T]TGATGTGTTGTTTTA | 17420 |
rs29168671 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73126075 | TCTGAGCTCAGGACC[G/T]TCTGTTTGCACAGCA | 17420 |
rs29169166 | snp | G/T | 0.473373 | 0.11227 | intron-variant | Mnat1 | Mm_Celera | 12:73169559 | AACTTCTTGCTGGAT[G/T]GTGTCTTGGTAATAC | 17420 |
rs29169317 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73272036 | CTTGTCTGGAAAAAC[C/G]GAAACAAAACAAAAC | 17420 |
rs29169952 | snp | G/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73213610 | TAGATTTTTTCCTTG[G/T]ACCAGTATGGAGTGT | 17420 |
rs29170701 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Mnat1 | Mm_Celera | 12:73209717 | TTTTTCTATGTAGTA[G/T]TTGAACACTAAATGA | 17420 |
rs29171144 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73244755 | GACCAGGCTGGCCTC[A/G]AACTCAGAAATCCAC | 17420 |
rs29171475 | snp | C/G | 0.492188 | 0.0620098 | intron-variant | Mnat1 | Mm_Celera | 12:73229010 | CTTGGAAAGTTCCCT[C/G]CTCTGACTTGTGCTT | 17420 |
rs29171665 | snp | A/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73153135 | ATTGTCTAATTTTTT[A/T]AACTTTTGTTGTGTG | 17420 |
rs29172128 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73241836 | AAAAAGAAAAAAAAA[A/T]TTTTAAAGCTCAAGA | 17420 |
rs29172218 | snp | C/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73259012 | CCAGGGATGGCACCA[C/T]CCCTAATGGACTGGG | 17420 |
rs29172306 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73204685 | AAAGAAGATATATTG[A/G]TAAAGCTATTTTGGT | 17420 |
rs29172419 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73197250 | ATACCATATGTTTGC[A/G]CAGCTGATATTCTAT | 17420 |
rs29173194 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73238737 | GCTAGACCAAGGGGC[C/T]TCTCTTCCCAGTGAT | 17420 |
rs29174812 | snp | C/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73224992 | AGATAGTATGCGACT[C/G]TCTTAGCCCCAACCT | 17420 |
rs29174967 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Mnat1 | Mm_Celera | 12:73199004 | ATTTTATTACATTTA[A/G]ACTTGGAGACTAAAT | 17420 |
rs29175316 | snp | G/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73224953 | GTATCTCAGGACTTG[G/T]CAATCTGCAATACTG | 17420 |
rs29176499 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73133723 | TTTTCCTAAGGATTT[C/T]TTGGTTCTATTGCTT | 17420 |
rs29177389 | snp | A/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73154883 | CTTTCTGACTCAACT[A/T]CTGCAGCTAGCTAGC | 17420 |
rs29177476 | snp | A/C | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73173961 | GTTTTTCTTTAAAAA[A/C]TAGAAACAGCACTGT | 17420 |
rs29178187 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73139277 | GGGATCCATTGCCAC[A/G]TGCATATTAGGCTAG | 17420 |
rs29178766 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73161131 | TTTATTTATTTGTTT[A/G]TTGTTTTGTTTTGTT | 17420 |
rs29179088 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73138004 | AAGAGGGAGTCAGAT[C/T]ACATTACGGATGGTT | 17420 |
rs29179496 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73238810 | CGAGCTCTGGGGGTA[C/T]TGGTTAGTTCACATT | 17420 |
rs29180473 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73133899 | TTATAAATATGACAG[A/G]TTTTTATTGTTCATT | 17420 |
rs29180731 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73238813 | GCTCTGGGGGTACTG[A/G]TTAGTTCACATTGTG | 17420 |
rs29181241 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73148293 | AATTTAATGTGTGTG[C/T]GCACACATGTGCCAC | 17420 |
rs29182020 | snp | A/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73176649 | TGTTATTGTAGGAAT[A/T]AAACTCTTTCAGAAT | 17420 |
rs29182291 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73144443 | TCTTTCACTCACACC[A/G]CTGCGGCTGGCTCAC | 17420 |
rs29182654 | snp | A/T | 0.5 | 0 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269551 | TACAACCAAATAGTA[A/T]GATCAACTATATTTC | 17420 |
rs29182898 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73175634 | ACCAAGTTGGCCTCG[A/G]ACTCACAGAGATCTG | 17420 |
rs29183241 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Mnat1 | Mm_Celera | 12:73223222 | TTTTCTAGATTGTTG[C/T]TTAAAGTAGTATTTT | 17420 |
rs29185062 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Mnat1 | Mm_Celera | 12:73224159 | GGTCACTGAGGAAAT[A/G]TAATTATGCAGTCTG | 17420 |
rs29185276 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73143324 | TATTCCTATTGATTC[A/G]TACATATACATATAC | 17420 |
rs29186595 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73184506 | TGTGTTTTCATGTTA[A/G]ATTTTTATAAAAAGG | 17420 |
rs29186724 | snp | C/G | 0.265928 | 0.249492 | utr-variant-3-prime, downstream-variant-500B, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73272902 | CCTTGTGTTTTTCTG[C/G]AACATATTTCCAAAT | 17420 |
rs29187581 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73144999 | CACTCTTTCATACGC[C/T]AGCTGGCTAGGGGCA | 17420 |
rs29189431 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Mnat1 | Mm_Celera | 12:73202941 | CACCCGCTCCCGCCT[C/T]GGCCCTGCTCGTTTG | 17420 |
rs29189904 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Mnat1 | Mm_Celera | 12:73223419 | GCATCTACGTTCCCA[C/T]GAGTGCTGACAAAGG | 17420 |
rs29190365 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73213785 | AGAAGAATTTCTTTT[C/T]TGGTCCAGTCTATTT | 17420 |
rs29190663 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73183543 | AGACATTTCTTGAGT[A/G]TTGACATGCTTCCAG | 17420 |
rs29191399 | snp | G/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73265148 | AGGACCATTTATGGT[G/T]GCTCACAACCACCTA | 17420 |
rs29191543 | snp | G/T | 0.487535 | 0.077957 | utr-variant-3-prime, downstream-variant-500B, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73272997 | TTTCCCCTTAATGTC[G/T]TATTGATAGTGGTAC | 17420 |
rs29191871 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73126021 | GCTGGGGTTACTGGC[A/G]CTTGAGGCCATGTGC | 17420 |
rs29192589 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73139639 | TTTGTGACAGGGGTT[C/G]TCTGTGTAGCCCTGG | 17420 |
rs29192824 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Mnat1 | Mm_Celera | 12:73202472 | ATAAGTAAATAATCC[C/T]TAGTCTGTTTTAAAA | 17420 |
rs29192920 | snp | C/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Six4, Mnat1 | Mm_Celera | 12:73111943 | GCCGGCAGCCCCTGC[C/G]GGCCCAGAGCTGCCG | 17420 |
rs29193059 | snp | A/G | 0.444444 | 0.157135 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | Mnat1 | Mm_Celera | 12:73123829 | AAAATCCAAAGCCGA[A/G]GAGACGCCATGGACG | 17420 |
rs29193373 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73192139 | AGAAGAGACCAGCAT[C/T]GTTGAGGTGACATCT | 17420 |
rs29193419 | snp | A/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73243555 | TAGCTGGAAAAAAAA[A/T]TTTTTTTCCTTTCCA | 17420 |
rs29194117 | snp | G/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73149015 | TCATAAATTGTGTGT[G/T]TTTTTTTTAAATCAT | 17420 |
rs29194131 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Mnat1 | Mm_Celera | 12:73200000 | GAATTGTTTACAACT[A/G]CCTGTGTTCCTAGAT | 17420 |
rs29194537 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Mnat1 | Mm_Celera | 12:73216694 | TGCACTGAGGGTCTC[A/G]GGTTACCAAGATATG | 17420 |
rs29194549 | snp | A/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73148002 | CACAAACACACACAC[A/T]CTGGCACATGCACAG | 17420 |
rs29195312 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Mnat1 | Mm_Celera | 12:73205900 | AGGAGCCGCTGAGGA[C/T]GCTCTAAGCTGAGGT | 17420 |
rs29196717 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73186810 | CTCTATAATCTGTTT[C/G]ACACACACACACACA | 17420 |
rs29196943 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73202402 | TTATGAGGATAAAAT[A/G]TATAAAGATAATTTC | 17420 |
rs29197090 | snp | A/T | 0.465374 | 0.126941 | intron-variant | Mnat1 | Mm_Celera | 12:73210268 | CCAGACATACATTCA[A/T]TTGGAGGACAATCTT | 17420 |
rs29197226 | snp | A/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73203085 | ATGGCAGCTTTCCCC[A/T]GGAACTGCTGTCCTT | 17420 |
rs29197342 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73176480 | GTGTACCTGCACTCT[C/T]TACACGCCCCTTTCC | 17420 |
rs29197403 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73118725 | CCCCAGTGATCCACT[C/T]CCCTCAACTTGGCCT | 17420 |
rs29197545 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Mnat1 | Mm_Celera | 12:73210080 | TTAAAAGATAAAGGG[C/T]CATAAAGGCTGATTC | 17420 |
rs29198956 | snp | G/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73161117 | TATTTATTTATGTAT[G/T]TATTTATTTGTTTAT | 17420 |
rs29199167 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Six4, Mnat1 | Mm_Celera | 12:73110677 | TGAAGTCAGCAGAGC[A/G]TGGCTCAGGATATGT | 17420 |
rs29199921 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Mnat1 | Mm_Celera | 12:73244333 | TTTTACAGTTTGTTT[C/T]AGATCTTGATTTGAA | 17420 |
rs29200636 | snp | G/T | 0.5 | 0 | intron-variant | Mnat1 | GRCm38.p3 | 12:73149013 | CCTCATAAATTGTGT[G/T]TTTTTTTTTTAAATC | 17420 |
rs29200719 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Six4, Mnat1 | Mm_Celera | 12:73113851 | CCTCCCCCCACCCCC[C/T]AAACTAAGGGATGTC | 17420 |
rs29201330 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Mnat1 | Mm_Celera | 12:73226583 | CAATGGGAAAAATAG[C/T]TCTCCCTACCATATG | 17420 |
rs29202088 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73144772 | GGCCCGATCTTCTGA[A/G]TGCTGCAGCTGGTGA | 17420 |
rs29202175 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73187237 | GCATCACTGAGCTGC[A/G]TCCCTTTCTCTTTTT | 17420 |
rs29202450 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Mnat1 | Mm_Celera | 12:73235124 | CACTGTAATCCTCTG[A/G]TGCAGTTTGGGTAAA | 17420 |
rs29202965 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73198995 | AGTTTAAACATTTTA[C/T]TACATTTAGACTTGG | 17420 |
rs29203426 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73260123 | TCCAGCTTCACAGGT[C/T]GTGGTGATAATTGGT | 17420 |
rs29203821 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | Mnat1 | Mm_Celera | 12:73246317 | CATGTTCCTCAGGTA[C/G]TAACTTAAGCTGCAA | 17420 |
rs29203934 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Mnat1 | Mm_Celera | 12:73197179 | AACCACCCTCTGCAT[A/C]TATTGGATCAGTTAC | 17420 |
rs29204142 | snp | C/T | 0.498615 | 0.0262793 | utr-variant-3-prime, downstream-variant-500B, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73272943 | TTATAACATTCAGTG[C/T]TATTATCCAAGTCTA | 17420 |
rs29204176 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73144437 | CAGCTCTCTTTCACT[C/T]ACACCGCTGCGGCTG | 17420 |
rs29204498 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73233669 | AAATAAAGGATCGGC[A/T]TGAGGATGGCCTAGT | 17420 |
rs29204897 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73241837 | AAAAGAAAAAAAAAA[A/T]TTTAAAGCTCAAGAA | 17420 |
rs29205084 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Mnat1 | Mm_Celera | 12:73209938 | AGGAATTCTTTGATA[A/G]ATTGAAGCATATTAT | 17420 |
rs29205419 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Mnat1 | Mm_Celera | 12:73199349 | GGTCTGTATCATCTT[A/G]ATTACACATTTTATT | 17420 |
rs29205608 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73256762 | TTGATGCTGACAATG[A/G]TAATGAAAATCAGTT | 17420 |
rs29205668 | snp | C/G | 0.484429 | 0.0868505 | intron-variant | Mnat1 | Mm_Celera | 12:73169990 | TTCATTTCCAAATCC[C/G]TGAAGTATGTTATTA | 17420 |
rs29207477 | snp | A/C | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73199462 | AGCTGTTTCTGTCAG[A/C]AAACACTGGGCAGTG | 17420 |
rs29208105 | snp | G/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73179066 | GATAGGAGAGATAGA[G/T]AAAAGACACAATAGA | 17420 |
rs29209242 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73200615 | TCCTTGTGTCCTACA[A/T]GGTAACGAATTGTAC | 17420 |
rs29209291 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73138391 | TGATTTTGTTCAATT[C/T]TTTCACCTGTTTGGT | 17420 |
rs29209306 | snp | G/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73198945 | TTCAACTTGTACGAT[G/T]CTGTCATGTGCTTGA | 17420 |
rs29209362 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Six4, Mnat1 | Mm_Celera | 12:73110689 | AGCATGGCTCAGGAT[A/G]TGTGTGTGTGTGTGT | 17420 |
rs29209579 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73198134 | AAGAGGGTGTCAGAT[C/T]TCATTATGGATGTTT | 17420 |
rs29209687 | snp | C/G | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73152038 | CTCTGCTATTAGCTG[C/G]TCAGGTAGTAGAGCT | 17420 |
rs29209759 | snp | C/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73177026 | GTACTGAGAAATAGT[C/T]AGAGATAAGAGAGTA | 17420 |
rs29210702 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Mnat1 | Mm_Celera | 12:73250806 | AGCCCTACTTAGTGT[A/G]TTGTCTCCGTGTCTA | 17420 |
rs29210810 | snp | G/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73161149 | TTTTGTTTTGTTTTT[G/T]TTTTTTTTTTCCGAG | 17420 |
rs29211134 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Mnat1 | Mm_Celera | 12:73200423 | TAAGGCTTTGTAAAA[C/T]AATTTTTTAAATTCC | 17420 |
rs29211350 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Mnat1 | Mm_Celera | 12:73211198 | TGAAAAGTTCTTGAT[C/T]CCAGTTTCATAGCCA | 17420 |
rs29212134 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Mnat1 | Mm_Celera | 12:73202024 | TGTACTTAGAAGATT[A/T]GTTTAGAGACAAAGA | 17420 |
rs29212461 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Mnat1 | Mm_Celera | 12:73249626 | ATTTTGTCTTGGTAA[A/G]ACCGATTGGCATGTG | 17420 |
rs29212793 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73222869 | AGATAGAGATCCAAA[A/G]CAAGTAAGGTTGCAG | 17420 |
rs29213029 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73119866 | CTGCTTTGAGAAAAA[G/T]TATTTTCTTCTTTTC | 17420 |
rs29213071 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73134795 | GATTACTTTTCTCTT[C/T]CCACTTTGTGGGTGG | 17420 |
rs29213145 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73165119 | TGTGGTGCACATACA[C/T]ACATGCAGGCAAAAC | 17420 |
rs29213210 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73235677 | GTGCCGCAAGCAGCC[A/G]CACTGGGGCTGGGGA | 17420 |
rs29213626 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Mnat1 | Mm_Celera | 12:73147310 | TGACCGTGGGATCTA[A/C]GTTTTGGGCAGCTGG | 17420 |
rs29214127 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Mnat1 | Mm_Celera | 12:73146306 | CCCAAAAGATCATCC[C/T]GTACTTATTTAAATT | 17420 |
rs29215019 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Mnat1 | Mm_Celera | 12:73202244 | AGAGTCCTTGGAGTT[C/T]GTTATTTCTAGGCCC | 17420 |
rs29215149 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73229748 | TTTTGTCTATTCTAC[A/G]TTTAATATGCCTGAT | 17420 |
rs29216139 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | GRCm38.p3 | 12:73240095 | AATTTAGAATGTTGG[A/G]TGCTTTTGTTTGTTT | 17420 |
rs29216169 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73124595 | TTCTCAGGATTGTGG[A/G]TCGTAGGAGTATGGA | 17420 |
rs29216367 | snp | G/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73267346 | AAGCCTTGCTTTTGA[G/T]ATGGCTTAGACATCT | 17420 |
rs29217446 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73177130 | GGCCGAGTTATAGGC[C/T]AGCCTGGATTGCAAA | 17420 |
rs29217514 | snp | A/C/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73213546 | CTTTTATGAATGTGG[A/C/G]TGCCCTTGCATTTGG | 17420 |
rs29218574 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Mnat1 | Mm_Celera | 12:73195061 | ACATTATGTTAATAT[C/T]AATGGAGCCCAAAGA | 17420 |
rs29218724 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Mnat1 | Mm_Celera | 12:73119391 | GTTCAGGTAGTTTTC[A/G]GAGGCAGGAAGCTTG | 17420 |
rs29218781 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Mnat1 | Mm_Celera | 12:73184107 | TCAAATCCAGTGAGG[C/T]GTGAAGTAAGACGTC | 17420 |
rs29218820 | snp | C/T | 0.455 | 0.143091 | intron-variant | Mnat1 | Mm_Celera | 12:73153611 | CATATACAGGACAAT[C/T]GGTAGGCTAATGAAT | 17420 |
rs29219337 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73232981 | CACATTTTAGTCATT[A/G]GTATTTAATGTTTTC | 17420 |
rs29220461 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Mnat1 | Mm_Celera | 12:73235749 | TTATAAATAGACTCC[G/T]GATAGGGTTGTGTGT | 17420 |
rs29220462 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73191851 | GATCCATTCGGGTGT[A/T]AAGAGCTCTGTTAGA | 17420 |
rs29220677 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Mnat1 | Mm_Celera | 12:73188354 | ACACTAAAGTGAATG[A/G]TTTAGATATTTAAGA | 17420 |
rs29220819 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Mnat1 | Mm_Celera | 12:73265335 | TACTTGTTCAGAATT[A/G]AGTGGCTGATACATG | 17420 |
rs29221163 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Mnat1 | Mm_Celera | 12:73219736 | TTTCTGAACAAAAGA[A/C]TATAATATGAAATAA | 17420 |
rs29222190 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Mnat1 | Mm_Celera | 12:73251868 | TTCCAGATTTAAACT[A/G]AAAATCGTCTTGTGA | 17420 |
rs29222245 | snp | A/C | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73216455 | GCTGTAGCCAGGTGT[A/C]CAGGCATGCTTCTGA | 17420 |
rs29222885 | snp | C/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73176493 | CTTTACACGCCCCTT[C/T]CCCCAACAAAAGGCA | 17420 |
rs29486012 | snp | A/G | 0.498615 | 0.0262793 | utr-variant-3-prime, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73273459 | GTGTGAGTCTGTCGC[A/G]TGGGCCCCTGGGTAT | 17420 |
rs29486994 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Mnat1 | Mm_Celera | 12:73124392 | TACGTGTCCTGATGA[A/G]TTATGTTAGACTTAA | 17420 |
rs29488159 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Six4, Mnat1 | Mm_Celera | 12:73115986 | AAGTAGATAAGAAGT[C/T]GCATGGTTTCATGGA | 17420 |
rs29488590 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73189900 | ATATAATATATTCTA[C/T]ATGTATCTAGTATTT | 17420 |
rs29488780 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Mnat1 | Mm_Celera | 12:73202571 | AGTAACTAAACCTAG[A/G]TGTTTATCAAATAAA | 17420 |
rs29489573 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Mnat1 | Mm_Celera | 12:73163985 | GCGTAACTGACGTAA[A/T]CAGGTATTTTTTCTT | 17420 |
rs29489860 | snp | A/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73230952 | CACACACACAGAATT[A/T]TCTGGGTGTTGAGGC | 17420 |
rs29489914 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73272204 | TTTTAACATTTCATC[C/T]AAATGTACAGGTTAT | 17420 |
rs29491071 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73228610 | AATTGGTATAATTGT[C/T]GTGATTCATTTAACT | 17420 |
rs29491632 | snp | A/T | 0.265928 | 0.249492 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269389 | ATGATCACAGAAGAA[A/T]AAACAGGTGTGGAGG | 17420 |
rs29492164 | snp | A/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73140150 | TTTTGTTTCTAGTGC[A/T]GGGGTTAAAACATGA | 17420 |
rs31023024 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73238973 | GAGACAGCTATATCA[A/G]GGTCCTTTCAGCAAA | 17420 |
rs33843334 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73252886 | AGTTCAGAGCTCTTT[A/G]TTAGGGAAAATATAG | 17420 |
rs33845015 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Mnat1 | Mm_Celera | 12:73236449 | TTCCATTTATACTTG[C/T]AATAAGCAAAGTTAA | 17420 |
rs33845097 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Mnat1 | Mm_Celera | 12:73199714 | TTCTACCGTAAATCA[C/T]TCATATAACAGAAAC | 17420 |
rs33845243 | snp | A/C | 0.475309 | 0.108333 | intron-variant | Mnat1 | Mm_Celera | 12:73202721 | AGCTGCTTTCTCCTT[A/C]ACTTCTTTGAGTTAC | 17420 |
rs33845866 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73241419 | TTTAAGGTTGAATGC[A/G]TGCTAATAGCATACA | 17420 |
rs33847363 | snp | G/T | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73260065 | CACCTGTCTTCTTCA[G/T]TCTTGATGGACAGCC | 17420 |
rs33847642 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73245005 | AGCCTTGCCTGTTGG[A/G]AGGGGCAGTGAGAAA | 17420 |
rs33882895 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | GRCm38.p3 | 12:73185960 | TTTAAATGAGAAGTG[C/T]TTACTTCTAAAAGTT | 17420 |
rs45639255 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | GRCm38.p3 | 12:73205892 | TCCCGAGGAGGAGCC[A/C/G]CTGAGGATGCTCTAA | 17420 |
rs45697295 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73130281 | TTTCATAGTAGGAAT[C/T]CCGTGGATGATAACA | 17420 |
rs45721436 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73160039 | CTCAAAACCTGAGAT[G/T]TCTGATTGGAGGCAG | 17420 |
rs45803956 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73159267 | TCATAGCATGGGCCT[A/T]ACCTGCCAGTAGTGT | 17420 |
rs45816674 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73272919 | ACATATTTCCAAATG[C/T]CTTTTTGATTATAAC | 17420 |
rs45835778 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73159020 | ATGCTATCTATACAT[A/T]ATGGTTGGAGCATGA | 17420 |
rs45838265 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73159230 | GGCCTCTGGAGGATA[G/T]TCAAGATTTAAACCA | 17420 |
rs45854351 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73214524 | CTGGAGCCCGTCCTT[C/G]CTGTGTCAGAACTCC | 17420 |
rs45857409 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73145704 | CTGTGCAGAACCCTG[A/C]ATTGGTTGTCTCATT | 17420 |
rs45872559 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73214764 | AAGGAACCTATGCCA[C/G]TGGTCTGGCGGAGTT | 17420 |
rs45881993 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Mnat1 | Mm_Celera | 12:73240592 | TGGCTATGAAATAAA[G/T]ACTAAGGCCAATCAG | 17420 |
rs45889345 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73214481 | CCATCTGAATATCTC[C/T]AGTGCTACCTGCTCT | 17420 |
rs45904089 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73209960 | GCATATTATCAAAAC[A/G]AGCATTGCTGATGAG | 17420 |
rs45948316 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73206415 | AGCTGTGTGCTCAGC[A/G]AAAGGGCTCAGTGCC | 17420 |
rs45961320 | snp | A/C | | | intron-variant | Mnat1 | Mm_Celera | 12:73239021 | CCATAAACAACTACC[A/C]AACCCAGACACTACT | 17420 |
rs45979176 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73200763 | CAGAGTTGTGATGGC[A/C]ATACGGCTTCACAGT | 17420 |
rs45979755 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73194049 | TTCAGAATTTATCCA[C/G]CCCCCCCCCCCCAAC | 17420 |
rs46030647 | snp | C/T | 0.18 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73167543 | TTTTTTTGGAAGGGT[C/T]ATGACAGTGCATTGG | 17420 |
rs46052028 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73228555 | TACCACCTAGCGAAG[G/T]TGTGCATAACTGGGC | 17420 |
rs46059032 | snp | C/G | 0.231111 | 0.249285 | downstream-variant-500B, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73274051 | AGAAAGAGCATGTCA[C/G]TGAAAAATGGCCATA | 17420 |
rs46060937 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73249378 | CACACTGGTTCCTCA[A/G]TGGCAAAGCCAGGGA | 17420 |
rs46072352 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73219200 | TACTTATAGAACTGA[A/T]TCCTGCTTCTCAAGA | 17420 |
rs46074419 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73231335 | AGTGATTCTTCACCT[A/T]ATCTTTTGAGGCAGA | 17420 |
rs46086739 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269933 | CTCAATGAGTATGAC[C/T]GTTTATTACATTTTC | 17420 |
rs46100712 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269812 | CGTTAATAACTCAAC[C/T]TTAACAATATTTGCT | 17420 |
rs46136643 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73205876 | TTAGAGAATAATCAG[C/T]TCCCGAGGAGGAGCC | 17420 |
rs46139037 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73273115 | GGGGACTGTTTTGAG[C/T]CATGCAAAGTGAGGC | 17420 |
rs46156091 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73130548 | GGCTTTGTTCCTTCC[A/C]GGCGTTGGAGCCCTG | 17420 |
rs46162109 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73214407 | GGTGGGAGAATTGGG[A/T]TCTGATGATGCCAAG | 17420 |
rs46231069 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, downstream-variant-500B, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73273077 | CAACTGTGATGTGGC[C/T]CTTCCTCAGCAGTAA | 17420 |
rs46247465 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73186940 | TGTTTATCGTCACAC[A/G]GTTCTGTTAGATTGA | 17420 |
rs46253708 | snp | C/T | 0.35503 | 0.226867 | utr-variant-3-prime, downstream-variant-500B, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73272985 | TAAAAACTTCTTTTT[C/T]CCCTTAATGTCGTAT | 17420 |
rs46268152 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73250899 | TCTGATTGTTTTAAA[C/T]GTTACTATTTACAGA | 17420 |
rs46274376 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73170500 | TTAAACCTGGCATAA[A/G]AACACAGTGTTGAAT | 17420 |
rs46281997 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Mnat1 | Mm_Celera | 12:73219659 | TGGATGTAAAGAATC[A/G]TTTTTTGGTCTGGTT | 17420 |
rs46282190 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73169562 | TTCTTGCTGGATGGT[A/G]TCTTGGTAATACTTT | 17420 |
rs46291959 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73244134 | TGATAACTCTCACAG[C/T]AATAAAACCTATCAT | 17420 |
rs46293419 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73209242 | AGGAAAGAGGTTTTT[C/G]TCTCACCAGATAGTC | 17420 |
rs46295912 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73164695 | TATGTAAACAAAATT[A/G]GCAGTGTGTTATAAG | 17420 |
rs46305361 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73223958 | AGCTTAGAAATGAGC[G/T]TGAACCTTGTGCTCT | 17420 |
rs46306985 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73241349 | GTATATAGAATAGCA[G/T]AATGCTGGAGTGGCT | 17420 |
rs46335880 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73199041 | TATTTGATGCCTTTT[C/T]CTCAAGCCTCACGGC | 17420 |
rs46350512 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73168333 | AGAACTGTGTGGTAT[C/T]TAACCTTTGCTGTTT | 17420 |
rs46350999 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73272616 | TTTGTAAAGTTCCAG[C/T]CCCGCAGCTGCACAG | 17420 |
rs46371326 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269744 | GCAGTCTTCAGTGCT[A/G]TGCAAAGAAACTTTA | 17420 |
rs46411937 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73244151 | ATAAAACCTATCATA[A/G]CTAACTTCATATGCT | 17420 |
rs46414856 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73241222 | GTATAGTGGATAGTG[C/T]CCAGTACCAAGATCT | 17420 |
rs46449967 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73181185 | ATATTGACTTATGTA[A/G]CAGGGGTTTAGGAAT | 17420 |
rs46458429 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73117247 | TAAGGAGTTGTTGTC[G/T]TCGTTGTTGTTATCA | 17420 |
rs46468299 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73169792 | CTCACAGAGATCCAC[C/T]TGCCTCTACTTCCCG | 17420 |
rs46482837 | snp | G/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73206662 | GTCTGATTCCAGATG[G/T]ACTTAAAGTAACTTC | 17420 |
rs46493327 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73195692 | CTGGAGCATGTGGCT[A/C]TTCAGGCAAGATAAC | 17420 |
rs46496989 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73145869 | ACTGATGCACATGTG[A/T]CACAGCAGCCACACC | 17420 |
rs46505019 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73129658 | CACATAAAGTAAAAA[G/T]TTTAAAAAAACATTA | 17420 |
rs46506769 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269613 | AAATATTTTGAAACA[A/G]TTAACAGTAAAAGTT | 17420 |
rs46525655 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73201297 | TGTTAACAGTGCTAA[C/T]TGATACAAGTGAGTT | 17420 |
rs46531966 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73214392 | TCCAAGACTTGCTAT[G/T]GTGGGAGAATTGGGA | 17420 |
rs46542683 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Mnat1 | Mm_Celera | 12:73205925 | TGAGGTACAGAGTGT[G/T]TGGAGGCTCACAGGA | 17420 |
rs46545120 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73190654 | TCTTAAAATGTCAAA[C/G]TGGGAGGTCTTTGAG | 17420 |
rs46561606 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73238478 | TATATTGGAAGTTTC[A/G]TTGAAATATGGTTTA | 17420 |
rs46565752 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73201180 | GTACCTGAAATTTAT[A/G]TTTTTGAAGTCTTTA | 17420 |
rs46568598 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73125349 | CCCTTCGAACTTCAT[C/T]CCAAATTCTCCACCA | 17420 |
rs46577142 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73271303 | GTTATTATGTTAGAA[A/G]TAGGAAGTTGCTCAT | 17420 |
rs46581118 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73200253 | AACAGGTTAAGCATG[A/G]GAGAGATCAGCCAAG | 17420 |
rs46624774 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Mnat1 | Mm_Celera | 12:73218560 | ATAGAAAGTAGGAAA[C/T]GTAAGGTTGAACTGA | 17420 |
rs46647044 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Mnat1 | Mm_Celera | 12:73201351 | AAGATGTACAAAATT[A/T]AAAAAAATGGTTATA | 17420 |
rs46671328 | snp | A/C/T | | | intron-variant | Mnat1 | GRCm38.p3 | 12:73138054 | CTGGGATTTGAACTC[A/C/T]GGACCTTCAGAAGAG | 17420 |
rs46672252 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Mnat1 | Mm_Celera | 12:73169865 | TAATATTTTTAAGGT[C/T]ATATTGTCATGAAAA | 17420 |
rs46679356 | snp | A/C | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73145734 | TAGCTTTCTGTCCAG[A/C]CTCCTGGTGCCCGTC | 17420 |
rs46684550 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73243474 | GACTGCTCTTCATTT[A/C]ATAATTTCAAATGAA | 17420 |
rs46687065 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73241555 | AAGAGCACAGGGTTC[A/T]TAGCAGAGAATATCA | 17420 |
rs46692200 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73200513 | AGCTCAGTGTTCCTG[A/G]AAATGGTAAGTGATT | 17420 |
rs46699894 | snp | C/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73152071 | TTGTCTTTGACTCAA[C/T]TCTATCCACTAGCTG | 17420 |
rs46739238 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73252539 | TAATTTCTTGAACAA[A/G]GTGAACTTTAAGAAC | 17420 |
rs46743542 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73151783 | AACCAACTTATTCTC[A/G]TTTAGTGTAACATGA | 17420 |
rs46751776 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73200719 | CGGATAGTACAAGCA[A/G]TAGAACCTGAACCCC | 17420 |
rs46786238 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73177260 | TTTGACTTTGGTTGT[G/T]TAGTAGAAGTGTAAA | 17420 |
rs46811836 | snp | G/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Mnat1 | Mm_Celera | 12:73123073 | AACAGGTACTAGATA[G/T]TATTTATAGAAGTAT | 17420 |
rs46813269 | snp | A/C | 0.231111 | 0.249285 | utr-variant-3-prime, downstream-variant-500B, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73273025 | TACAGACAAGTGGAG[A/C]TGTTTCATCTTAGCA | 17420 |
rs46823686 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73124561 | ATAGTTTCTTCCTCA[C/T]CGGAAATGATCCTGA | 17420 |
rs46827583 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73220802 | TAGCACAGACGTTGG[C/T]TTAAAAGAACTTTGG | 17420 |
rs46839971 | snp | A/G | 0.5 | 0 | intron-variant | Mnat1 | Mm_Celera | 12:73200583 | ACTACCCTTTCCTCA[A/G]AGGTTGTCAAGCTAG | 17420 |
rs46868937 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Mnat1 | Mm_Celera | 12:73173214 | GATGTATCTTTAAAG[C/T]AGGTAGAAATTCTCT | 17420 |
rs46910273 | snp | C/T | | | intron-variant | Mnat1 | GRCm38.p3 | 12:73167008 | TAGTTGAGGTTACTT[C/T]TAACCTCAAGATGTA | 17420 |
rs46924914 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73117331 | TCAAAGGACATTTCT[A/G]TGGAATCAGTTAGCA | 17420 |
rs46937106 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Mnat1 | Mm_Celera | 12:73118917 | TCAGGAACAGAGCTG[A/G]TAGACTAAGACCTGC | 17420 |
rs46937750 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Mnat1 | Mm_Celera | 12:73171034 | GTTCACTGTCACTTA[C/T]GCTGTCGTGCAGCAG | 17420 |
rs46944469 | snp | A/G/T | 0.132653 | 0.220748 | intron-variant | Mnat1 | GRCm38.p3 | 12:73164707 | ATTAGCAGTGTGTTA[A/G/T]AAGTGAGGTCTAGAG | 17420 |
rs46950198 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Mnat1 | Mm_Celera | 12:73181371 | TAATGAGGCTATAGT[A/G]TTAGAGTGCAGCTCC | 17420 |
rs46973054 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Mnat1 | Mm_Celera | 12:73211319 | TGTAAATAACCCTAA[C/T]GAATACAAGTAGAAA | 17420 |
rs46997266 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73226515 | GGAGCCTCTCACTTT[C/G]CACTGTCATTGGACT | 17420 |
rs47005271 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73152742 | GGAGTGTAATCAAAT[A/G]GGCTGATAACCTCCA | 17420 |
rs47005310 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73243513 | TTCTGTTTTTCGCTT[G/T]ACTGCTTTTTAAAAG | 17420 |
rs47006278 | snp | C/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73206117 | TAAAGACAGCAAGGC[C/T]GGTAATTGTTTGAGG | 17420 |
rs47011221 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73200816 | TGGCGCTGTGACTTA[A/G]AGCCTATGGGACCTG | 17420 |
rs47025994 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73181932 | ATGAGCTGGTAAGCA[C/T]GATGCAGTTACCTCT | 17420 |
rs47026125 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73242531 | AGAACTTGGGTGTTA[C/G]TAGAACATTGGCTTG | 17420 |
rs47066839 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73225555 | CTTAGGAGGGAAGGC[C/T]TAGTTGTTGAAGGCT | 17420 |
rs47093247 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73142726 | TAGAGTGTTACTTTG[C/T]ATTGGATTTAAATTA | 17420 |
rs47094167 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73228963 | ACGGTGAGCTTTTGT[A/G]AGCATAGCCAAGATA | 17420 |
rs47096601 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73244845 | TTACACATTTTAAAC[G/T]TCAATATACTTTAAA | 17420 |
rs47098590 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Mnat1 | Mm_Celera | 12:73228936 | CTTTACCCGCATGAT[G/T]AAAGGCTAGGGACGG | 17420 |
rs47117004 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Mnat1 | Mm_Celera | 12:73184129 | TAAGACGTCCTTCCC[A/G]GTGCCGTCCGTTGTG | 17420 |
rs47162406 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73236971 | TCAGTTTTTGCCCAC[C/T]AACCGCGACTACTGA | 17420 |
rs47170309 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Mnat1 | Mm_Celera | 12:73223468 | AGCCACAGCCACAGT[C/T]ACAGCAGTGACTGTT | 17420 |
rs47210464 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Mnat1 | Mm_Celera | 12:73184265 | TAACAGGGTGGTTAA[A/T]TAATTCTTAGTAATT | 17420 |
rs47222767 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Mnat1 | Mm_Celera | 12:73152919 | ACATAAAAATGCTAG[A/C]TATCTTGCAGATCTG | 17420 |
rs47227924 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73178452 | ACTCAGCTAGGCAAG[C/T]ATTTGCAGAAACAAC | 17420 |
rs47236306 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Mnat1 | Mm_Celera | 12:73147790 | TCAGATTGTACTCTG[C/G]GCTCTCAGTCAATTG | 17420 |
rs47251312 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Mnat1 | Mm_Celera | 12:73168496 | AAATTTACAATAAAG[A/C]CTAAAGAGGCAACAT | 17420 |
rs47275106 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73146958 | GTGTAGGAAGCCAGA[C/T]TTTGGGTAGCTCTTC | 17420 |
rs47331845 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Mnat1 | Mm_Celera | 12:73166351 | CTTGGGCATGTTGCT[C/T]TGCATGGGAAATGAA | 17420 |
rs47340661 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73189795 | TTAACTGCTCCTTCA[C/G]ATTTATATAGTATTC | 17420 |
rs47354859 | snp | G/T | 0.18 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73167041 | AGAAATGAAATATTC[G/T]TTTGCCTTGAAGTTC | 17420 |
rs47373764 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Mnat1 | Mm_Celera | 12:73178247 | AGAAAGTGGACAAGC[G/T]GAAGAGACTGCTAAG | 17420 |
rs47378502 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73214966 | CACTGGTCCAGATCT[G/T]CTTTAAACTCTTGAA | 17420 |
rs47400767 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73244389 | GGGGAAACCTCTCAG[C/T]CAGGTTTGCAGTGAG | 17420 |
rs47418087 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Mnat1 | Mm_Celera | 12:73172089 | CCACATACAAGAAGT[C/T]GGTGTGATTAGTATG | 17420 |
rs47421931 | snp | C/G | | | upstream-variant-2KB, intron-variant | Six4, Mnat1 | Mm_Celera | 12:73116769 | ATGCTGTGTTGTGAT[C/G]TTGAAGAGTGGAAGA | 17420 |
rs47432900 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Mnat1 | Mm_Celera | 12:73176838 | TTCTAAAACAGGCCC[A/T]CTAAGCTTTTAGCCC | 17420 |
rs47433101 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73196176 | AGCCTCTGCTTACCC[A/T]CCCCCAACCACCGGG | 17420 |
rs47452629 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73164163 | AGGTTTTGAAGGTAG[A/G]GTTTGCTCTATAAAC | 17420 |
rs47458976 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73117424 | CAATCCCAGAAAGGG[C/T]GTTTCCATTTCCAAG | 17420 |
rs47500149 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73209528 | TGCCCTCCATAGTGC[C/T]CAGGCTTACTGTGGT | 17420 |
rs47500296 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73142624 | GTCTGGTTTGTCCCT[G/T]CCTACTACGTTTTTC | 17420 |
rs47511270 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73124167 | ACCCTCATCCACCTT[C/T]CCAGCCAGTGAAAAT | 17420 |
rs47518916 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269479 | CTTAAAGAGCTTCGG[A/T]ATACCAGAATTATTA | 17420 |
rs47528599 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73241230 | GATAGTGCCCAGTAC[C/T]AAGATCTTCTTCCTC | 17420 |
rs47530099 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73193645 | TGGCAGAAGCTGAAA[A/G]ATTAGTTCAGTCATT | 17420 |
rs47554912 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Mnat1 | Mm_Celera | 12:73123398 | CACAACTATGAAGAC[A/G]TCTACAGTACAGACT | 17420 |
rs47558046 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73242444 | CAATGTCAGTCTTGC[C/T]GTGTAACCGAGAACC | 17420 |
rs47569879 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73234916 | CATGGATTTCATCAG[A/G]ATCTCAGAGGGATCC | 17420 |
rs47608729 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73207241 | AGGCAGCTGATTGGC[A/G]GCAGCACCTGTCCTA | 17420 |
rs47612824 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Mnat1 | GRCm38.p3 | 12:73167106 | GAATGGCTGCTATAC[C/T]TGTAGAACTTTTTGT | 17420 |
rs47644960 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73227270 | TTTAACAGGGTATAC[A/G]ATTGCCCTTCTTGTT | 17420 |
rs47657096 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73128733 | AATTCGTGTACATGT[A/G]TTACATATGCACAAA | 17420 |
rs47671714 | snp | A/G | 0.18 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73169229 | AGAGCCAAGCACACC[A/G]CCCTCACAGCCAGCA | 17420 |
rs47672211 | snp | A/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73203466 | GCATTAGGTTCTAGA[A/T]TGGGACTGCAGAGGA | 17420 |
rs47672415 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269845 | CTGCATTGGATTATG[A/G]CTGTTCAAGAAGTAC | 17420 |
rs47677842 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73130522 | AGTCCCAGGAACAGA[C/T]AAGCTCCAGAGGCTT | 17420 |
rs47700111 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73165525 | TAATAAGGAACCCAT[C/T]TGCTCTATATATGTC | 17420 |
rs47702514 | snp | A/C/G | | | intron-variant | Mnat1 | GRCm38.p3 | 12:73223582 | GGAGAGTATGGCATG[A/C/G]TATGTATACTTTGGT | 17420 |
rs47724361 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73199583 | GCAAAGGCAAGAAAA[A/G]AGGGGGGTGGCAGAT | 17420 |
rs47724708 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73210241 | TTGTTTTTTTTTTTT[A/T]AAATATGTAAACCAG | 17420 |
rs47752848 | snp | G/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73159795 | TCTTGCCAAGAGTCC[G/T]ACTTATAGGAAAAGA | 17420 |
rs47766088 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73161932 | CAGCAAATGTGTTTA[C/T]TGTCAAAATATTCTT | 17420 |
rs47769630 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73252744 | CTCTTAAACTTCTGA[C/T]CCTGATGTCTCAGTC | 17420 |
rs47770486 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73235133 | CCTCTGGTGCAGTTT[G/T]GGTAAATTGCCATCT | 17420 |
rs47787824 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73195485 | GTTAAGGTCAGCTTT[A/G]AAAATCCTAGAAGAA | 17420 |
rs47801325 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | GRCm38.p3 | 12:73236925 | TCTGGGCAATTTGAC[A/G]AAGGGCCAGCAGACT | 17420 |
rs47813168 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Six4, Mnat1 | Mm_Celera | 12:73114554 | TTGTTTGCATATGCT[C/T]CTTCTCAAACTCTTA | 17420 |
rs47826629 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73225217 | TGCTTTGTATTCTAA[A/G]ATATTTCAGAGTGGG | 17420 |
rs47858279 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Mnat1 | Mm_Celera | 12:73188744 | TTTCAGAAATATTTT[C/T]AAAGCTTTTTTAATT | 17420 |
rs47875349 | snp | C/G | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73242470 | GAACCCATTATTTAT[C/G]CTGAGGAACCCAGCA | 17420 |
rs47894386 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73148867 | ATAAAATGACCTAGT[C/G]TTTGAATTTATATTA | 17420 |
rs47894802 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269824 | AACTTTAACAATATT[C/T]GCTCACTGCATTGGA | 17420 |
rs47895552 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Mnat1 | Mm_Celera | 12:73172060 | AAGCAGAACAGCCAT[C/G]ACAAAGAAAGTTTCC | 17420 |
rs47902538 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Mnat1 | GRCm38.p3 | 12:73211941 | TTGATATACATATTT[A/G]TAAACACAACACTGC | 17420 |
rs47910187 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73201350 | AAAGATGTACAAAAT[A/T]TAAAAAAATGGTTAT | 17420 |
rs47919581 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73164111 | TGGGCCACCAGAAAG[C/T]GGTTAGTCAGGGCTG | 17420 |
rs47920867 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73270041 | AGGTATTTTACGGGG[C/T]CTGGGCTTGCCTGCC | 17420 |
rs47921298 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Mnat1 | Mm_Celera | 12:73170269 | GTGATACCATTCTCT[C/T]CTGATTCTACAGTTT | 17420 |
rs47946585 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73208868 | CCTAATGTACCAAGC[A/G]CTGCATCAGACATGG | 17420 |
rs47958193 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73164258 | TGGTTCAAATTTACG[A/G]TGATTCTACTGCCTC | 17420 |
rs47964162 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73164762 | GTATGCTTTATGTTG[C/T]TTGAACATTAATGGC | 17420 |
rs47999878 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73273889 | CTGATGAAGAAGTGA[C/T]GAAAATGAGCCCACG | 17420 |
rs48003519 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Mnat1 | Mm_Celera | 12:73185555 | ATAAAAGGGTTAGCT[A/T]CCTAGTGTAAGTGCT | 17420 |
rs48041394 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73175733 | CTTATTAAATAAATA[C/T]ATGCATTTTCAAGAG | 17420 |
rs48047405 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73221188 | TCTGAGCAATCCGAG[G/T]AGCCTCAGAGTAGTG | 17420 |
rs48047836 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73173200 | GTATATTTTATGAGG[A/G]TGTATCTTTAAAGTA | 17420 |
rs48063539 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73193429 | CACTTATAGCAACGT[C/G]CATTTTATAGTGTAT | 17420 |
rs48083906 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73215137 | GGGCGTGGTACATGC[C/T]TTTAATCCCAGCACT | 17420 |
rs48084419 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73199543 | CTGCTTTACTCCTGT[A/T]AGTGTCACTGTGAAC | 17420 |
rs48096580 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Mnat1 | Mm_Celera | 12:73222177 | TCAATTGAAAACATT[A/G]AAGTTCACTAAATGT | 17420 |
rs48121993 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73207902 | ACCAATGTAGCTTGC[A/C]TAAGTCTAAATGTAT | 17420 |
rs48147879 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73244520 | TTAATGAGGAGACTA[A/G]GCTAAATAATTATGA | 17420 |
rs48149689 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Mnat1 | Mm_Celera | 12:73207773 | ATTGACAAGTCATCA[C/G]TTTCTGTTGATGACT | 17420 |
rs48160975 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Mnat1 | Mm_Celera | 12:73238395 | AGGAGCAGAGAGGTC[A/T]TTGTGCTTACTCAGC | 17420 |
rs48168155 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73165425 | CTTGCTAGGAAGGGG[G/T]ACATCCTTTTTTTAT | 17420 |
rs48184878 | snp | A/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73225379 | TCTCCTCACACCACA[A/T]CTTTGAACAGGTCCT | 17420 |
rs48192823 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73227755 | TGTGTGTCAAGAAAT[A/G]CTGTAATGCCTTAAT | 17420 |
rs48194809 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73211863 | TAGATCAGGCTGGCT[C/G]TGCCTACCAAATGCT | 17420 |
rs48200500 | snp | G/T | 0.124444 | 0.216185 | downstream-variant-500B, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73274109 | TCACCCTCCCAGTGA[G/T]GTCCTCCTAGAGACA | 17420 |
rs48204184 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73145743 | GTCCAGACTCCTGGT[A/G]CCCGTCTTCTCAGGC | 17420 |
rs48214140 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73226301 | CACCGTAGCTGTGTG[C/T]ATGCAGGCCTGTGTC | 17420 |
rs48251140 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73229121 | CATTGTGCAGATAAA[A/G]TAAATAATAGATGCT | 17420 |
rs48279263 | snp | C/T | 0.18 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73176619 | TATCACTTTGTTGTG[C/T]GGCATTGTTCTGGTT | 17420 |
rs48295800 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73251585 | GCATACAAATAATAT[A/G]TGTGAGTGTATTGCT | 17420 |
rs48298047 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73205950 | ACAGGAGAACCACTC[C/G]CAAAGGAAAGTCAGA | 17420 |
rs48307792 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73117287 | ATTGTGTGTCGGTGT[A/G]TATATGTGCTACAGA | 17420 |
rs48320339 | snp | C/G | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73201732 | GCCTTGTTTTCTTGA[C/G]TGAAATACTAGAGTT | 17420 |
rs48324138 | snp | C/T | 0.165289 | 0.235211 | upstream-variant-2KB, intron-variant | Mnat1 | Mm_Celera | 12:73123356 | ATTCTAATCTTCATA[C/T]ATGTGAATCAAATTA | 17420 |
rs48324304 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73215112 | ACTTTAAGAAGGTAT[C/T]TTATAGGCCGGGCGT | 17420 |
rs48326281 | snp | C/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73148675 | GGACTGGGTTTATCG[C/T]TACAGAGTGAGCTTT | 17420 |
rs48327575 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73246301 | GAAATTTTACTTTAA[A/G]CATGTTCCTCAGGTA | 17420 |
rs48330963 | snp | G/T | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73273831 | TATGTTAGTTAGGTT[G/T]TTGCTAATTGGTAGT | 17420 |
rs48341944 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73246475 | CTGTCATAAAAAGTC[A/G]TAAGTGATTTGTTAT | 17420 |
rs48372601 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73194832 | AAAGAGTTTTCATTG[C/T]GGGAGTGAGACACTG | 17420 |
rs48389929 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73186933 | ATGTGCATGTTTATC[A/G]TCACACAGTTCTGTT | 17420 |
rs48399550 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269416 | GAGGCAGGCGGGGAA[A/G]TAGGCAAACCCCTAA | 17420 |
rs48443765 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73124992 | TTTCCTAATTAACTT[A/T]TATTTTGCTTTAGAC | 17420 |
rs48457695 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73160141 | AAGGGTATTTGATGT[C/T]CTCAACTGATAGGAT | 17420 |
rs48486195 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Mnat1 | Mm_Celera | 12:73219933 | CATAAAGTGAAAATG[A/G]CATATTATTTGATTA | 17420 |
rs48512013 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73208880 | AGCGCTGCATCAGAC[A/G]TGGAGTATGTATGAC | 17420 |
rs48521942 | snp | A/C | | | intron-variant | Mnat1 | Mm_Celera | 12:73117237 | TCTTTAAAATTAAGG[A/C]GTTGTTGTCGTCGTT | 17420 |
rs48524183 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Mnat1 | Mm_Celera | 12:73189064 | TAGTTGTATATGAAT[C/T]AGTAGTTTTATTTTT | 17420 |
rs48542183 | snp | A/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73159128 | TTTGCCATGCAAGCA[A/T]GAAGACAGAGCCCTT | 17420 |
rs48552257 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73247832 | TATTTCATTGTAATA[A/G]TATTTTTTAAATGTA | 17420 |
rs48561144 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73236985 | CCAACCGCGACTACT[A/G]AACGCCAAAAATCAA | 17420 |
rs48561271 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73249274 | AGAGTAGGCCATACA[A/T]TCATAGAAGTATGCC | 17420 |
rs48566466 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73117313 | ACAGATCATGTGTGG[C/G]AGTCAAAGGACATTT | 17420 |
rs48573943 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73139674 | CCTGGAACTCACTCT[G/T]TAGACCAGGCTGGCT | 17420 |
rs48579165 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73172123 | AGAAACCCTGGGATA[A/C]AAAAAGGCAAAAGAG | 17420 |
rs48585831 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73207512 | TGTGTGAGCTGCACT[C/T]ATGCTGAGCGATATG | 17420 |
rs48600219 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73232830 | AATCCTAAAGAGTGG[A/G]AATGGAAAACAGGGA | 17420 |
rs48620978 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73240430 | CCTGACCTTCTAATG[C/T]CAAAAGGTCTACATT | 17420 |
rs48623897 | snp | A/G | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73126900 | AAGATGGTATATGGA[A/G]TGAGAATAATGAGAA | 17420 |
rs48639714 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73206470 | GTGAGGATTTGCACC[A/G]CAGCAAAGCGCACAA | 17420 |
rs48647832 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Mnat1 | Mm_Celera | 12:73170964 | GCAACAGGAAGTGCC[C/T]TGATTGACTTGGTAG | 17420 |
rs48650944 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73227268 | CCTTTAACAGGGTAT[A/G]CGATTGCCCTTCTTG | 17420 |
rs48678025 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73245935 | AGACATTGCCAGGTG[C/T]GAGGGAAGAAAGGCC | 17420 |
rs48699051 | snp | G/T | | | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73270551 | TGTTTGCCCTTTTTT[G/T]GGGGGGGGGACAGGG | 17420 |
rs48701308 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269783 | ATTTTGGCAATGAGA[A/G]TCACACAACTTACCG | 17420 |
rs48702351 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73239104 | CATGGAACAAGTTAC[A/G]GAGTCAAAGTTTAGA | 17420 |
rs48711545 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73203140 | TATAAATTGTGCCTA[A/G]TTGGGTTCTGTCGTT | 17420 |
rs48711561 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73238967 | GAAAGGACCCAGATA[G/T]AGCTGTCTCTTGTGA | 17420 |
rs48718797 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73199451 | ACACTCTCTGTAGCT[A/G]TTTCTGTCAGCAAAC | 17420 |
rs48725808 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73240798 | CAGACTTACCATAGC[A/G]TGTCACCTCACCTCT | 17420 |
rs48729446 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73161759 | TAAAGACAAGGAAAT[G/T]TTTCATCAGTTTTTT | 17420 |
rs48739156 | snp | C/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73246776 | GTCAATGCATCGTTA[C/T]TGAGCAATATTGGTA | 17420 |
rs48757334 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73178286 | TTTTTGGCATTCACA[A/G]AAGGGGAATTGTCAG | 17420 |
rs48762607 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73199636 | GTTCTGCGGCCTTGT[C/T]TGTTTTGGCTAGTTC | 17420 |
rs48777234 | snp | A/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73148229 | GTGCCTCCTGCTTTT[A/T]GAGTGTCTCCTTTTC | 17420 |
rs48778066 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73226318 | TGCAGGCCTGTGTCT[A/G]TGTATGCATACCACA | 17420 |
rs48779394 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73239018 | TAATCAGCCACCAAA[C/T]GCAGACACTATTGCA | 17420 |
rs48782320 | snp | C/T | 0.35503 | 0.226867 | upstream-variant-2KB, intron-variant | Mnat1 | Mm_Celera | 12:73123350 | AGCATTATTCTAATC[C/T]TCATATATGTGAATC | 17420 |
rs48798086 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Six4, Mnat1 | Mm_Celera | 12:73110365 | TCCTCTTTGGTTTGA[A/G]TCTGGGCGGGGCAGG | 17420 |
rs48828808 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73270876 | CTCAGAGGCGGGTAG[C/T]ATGGCATGATTCATG | 17420 |
rs48833815 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73209301 | TTTATAGAAACAGAC[A/G]TGATTTGCTGGACAC | 17420 |
rs48850350 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269849 | ATTGGATTATGACTG[C/T]TCAAGAAGTACTATT | 17420 |
rs48850760 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73272316 | CATTTCAATCTTGGA[A/C]TTCCTTTCCAAATGT | 17420 |
rs48854943 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73124598 | TCAGGATTGTGGGTC[G/T]TAGGAGTATGGATCC | 17420 |
rs48881220 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73221248 | CTATTGTAACATCTT[A/C]TAGCAAAACAGGAAT | 17420 |
rs48910341 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73248594 | CCTAGGAGCAGCCAG[C/T]TTGGATTGCCTGTTT | 17420 |
rs48914982 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73232544 | TATAACTGGTTTCTG[A/T]CCTGAGTAACAGTTG | 17420 |
rs48935606 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Mnat1 | Mm_Celera | 12:73152141 | TTTAGAAGTTAATGG[A/G]CTGTTTTGTTTGGAA | 17420 |
rs49000115 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73147796 | TGTACTCTGCGCTCT[C/T]AGTCAATTGATTGAC | 17420 |
rs49002163 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73126811 | TTCTCCAAGTAAGTA[A/C]ACATACGTAATAAAA | 17420 |
rs49012041 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73214935 | TGTGGAGTTCACACC[C/T]AAGGTCTGCTCAGGG | 17420 |
rs49012605 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73167665 | GGTATCCTCTCAGTT[A/G]TCTGAAAAGTAATTG | 17420 |
rs49013466 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73127538 | GCCAGGTGTGATGCA[C/T]GCTTTTAACCTTAGC | 17420 |
rs49043183 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73190105 | TGTAATTATTTTCTT[A/G]CACCACCACTGTCCC | 17420 |
rs49049988 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73134728 | TTTTTGAGGTAGGGT[C/T]CTAATTTGTTTTTTA | 17420 |
rs49050546 | snp | A/T | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73273420 | TTGGGTGTGTGTTGG[A/T]CAGAAGCATGAGCAT | 17420 |
rs49085805 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73246849 | TTAAAATTGTGTATC[C/T]AATGTAGGTTTTAAT | 17420 |
rs49112136 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Mnat1 | Mm_Celera | 12:73181725 | TAAAGTAGAAGACCA[C/T]GGTAAAGGGTTGCTA | 17420 |
rs49115505 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73252639 | TTTGAGAGATGAGTA[A/G]TAATCCCTGGAATTC | 17420 |
rs49139178 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Mnat1 | Mm_Celera | 12:73225962 | TTTCACATTGTATAT[C/T]TGTTTTTGTTTGTTT | 17420 |
rs49146534 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, downstream-variant-500B, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73273035 | TGGAGATGTTTCATC[C/T]TAGCAGCAGGCCGTG | 17420 |
rs49148622 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73207647 | CAGCTTAAAGAACTG[A/C]TTAGCCAAGTGGCTC | 17420 |
rs49220410 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73206678 | ACTTAAAGTAACTTC[A/G]ACAGCACCTTGTAGC | 17420 |
rs49249694 | snp | C/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73207953 | ATTTTCTGCCAATGG[C/T]ATTTTATCATTTTCA | 17420 |
rs49259057 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73151947 | CTTGTCTAGAGCTTC[C/T]GTTAGTCTTGAGAGC | 17420 |
rs49277004 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Mnat1 | Mm_Celera | 12:73201378 | TATAGAATCTTAAGC[C/T]TTTTAGAGAATGGAG | 17420 |
rs49282531 | snp | A/G | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73154228 | ATGAACATTTAAGCT[A/G]TAGGAACAGATCAGG | 17420 |
rs49284997 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73243191 | CTGCCTTTAGGTGGT[A/G]GTTCCTTTTGGATGA | 17420 |
rs49296913 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Mnat1 | Mm_Celera | 12:73184031 | GGTGGACTTCCGGAG[C/T]TGTCAGTCCTCAGCA | 17420 |
rs49297902 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73249921 | CCATCATCCGTGGTC[C/T]AGAAACTGAAGTCAG | 17420 |
rs49312690 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73197658 | CTTACATGGTGGTTA[G/T]TTGTATATTCAAGAG | 17420 |
rs49318351 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73191256 | AATATCTAATGTAAC[A/G]TCAAGGATCCATAAA | 17420 |
rs49324516 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73127197 | TTATCATCTCTCTCT[A/C]TATATGTTATCCTTA | 17420 |
rs49364771 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73197212 | AATGTCCTCAAGTTC[C/T]ATTCATGCTGCTGAG | 17420 |
rs49389968 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73215132 | AGGCCGGGCGTGGTA[C/T]ATGCCTTTAATCCCA | 17420 |
rs49409958 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73230332 | ACTACTACAAAAAAT[C/T]TGCTAGAATTAAACA | 17420 |
rs49418044 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73211305 | TCTTTCCTGTGCCAT[A/G]TAAATAACCCTAATG | 17420 |
rs49421512 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73140975 | GTGCAGATTGGAATC[A/G]CCCCAAAGAACTTTC | 17420 |
rs49424696 | snp | A/C/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73172579 | TAACAGGACAGAGTA[A/C/T]GCTTGGATAAGTATG | 17420 |
rs49450783 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73238972 | TTGCTGAAAGGACCC[A/T]GATATAGCTGTCTCT | 17420 |
rs49450839 | snp | C/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73158240 | AGGTGTTTTGTTAAG[C/T]GTAGTATTAAGAAAC | 17420 |
rs49464588 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73194968 | TATTTCTGTGTTTGA[C/T]GTATAAACTTTGCAA | 17420 |
rs49470629 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73124814 | AGCACAATATTCCTA[A/T]AGGCTCAGTCTTCCT | 17420 |
rs49476501 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73170318 | TTTAAGAATAGTGTT[G/T]TTGGGTTGCATGCAT | 17420 |
rs49515583 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73193547 | TGGATGGGATTTGCA[G/T]CTTTTTGGTTGACAG | 17420 |
rs49522117 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73142824 | GAAAAGATAAGTCCA[C/T]TCCACATATATTTTG | 17420 |
rs49527134 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73195680 | TAACCAGTTTCACTG[G/T]AGCATGTGGCTCTTC | 17420 |
rs49595019 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73235210 | TGACCTGGATTCAGG[C/T]TTTCCTATTTCATCT | 17420 |
rs49607779 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73200858 | TGGTCATCTTTACAC[C/T]GTACCTTGCAGTGTG | 17420 |
rs49619470 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73152782 | AAGAGAATGATGAGA[A/G]AGCTAAACACAAGAA | 17420 |
rs49647301 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Mnat1 | Mm_Celera | 12:73181171 | AGCTTGTGTGAAGTA[C/T]ATTGACTTATGTAAC | 17420 |
rs49648523 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73119125 | GTTTTCCTTTTGAGG[A/G]CCTGCATCCTCCTAG | 17420 |
rs49652875 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73117706 | GGTTGAATTCTCATG[A/G]GGGAGAGAAGACATA | 17420 |
rs49656170 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73250875 | ACTGTAACCACCAAC[A/G]CTTCACTATCTGATT | 17420 |
rs49661889 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73251929 | ATAGGAAAAAATGCA[G/T]CAGGTAACAGGATGT | 17420 |
rs49693078 | snp | C/G/T | | | intron-variant | Mnat1 | GRCm38.p3 | 12:73170098 | GGAGGCAGAGGCAGG[C/G/T]GGATTTCTGAGTTCA | 17420 |
rs49719535 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Mnat1 | Mm_Celera | 12:73183425 | TACTTATTATAACCA[C/T]TTGTGATACTGATGA | 17420 |
rs49728281 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Mnat1 | Mm_Celera | 12:73181641 | AATAACAAGTGTCCT[A/G]GTTGCTCTGTACAGA | 17420 |
rs49736077 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73239065 | GTGGGGCAGTCTCTG[A/T]ATGGTCCTTCCTTCT | 17420 |
rs49738343 | snp | G/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Mnat1 | Mm_Celera | 12:73123028 | AATTCAGCTTGCCTG[G/T]CAGTCTTGAGGGGAA | 17420 |
rs49742986 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73203531 | TTGAAAGCCTTGCCT[A/G]AGTACCAGCCATGCT | 17420 |
rs49784731 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73200587 | CCCTTTCCTCAAAGG[C/T]TGTCAAGCTAGTTCC | 17420 |
rs49795771 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73270916 | ATCTCTTCAGGTTTT[C/T]ATTTCTATACATTTC | 17420 |
rs49801152 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73160643 | GACTTTAGAGTGGGA[C/T]GATGCCAGTAATGGC | 17420 |
rs49823379 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73167505 | TAGCCCCATTCTGGC[A/G]TTTGCATTGGGAGTG | 17420 |
rs49826431 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269688 | ACTCTTAAAGACCCC[A/G]GCCAGACATGCTCAG | 17420 |
rs49834935 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mnat1 | Mm_Celera | 12:73215029 | TAATTTTATGATTCA[A/G]TGAATTTTAATTAGT | 17420 |
rs49853587 | snp | A/G | 0.18 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73167691 | AATTGCCAAATAAAA[A/G]TGGTATTCCAAAGTT | 17420 |
rs49867096 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73223741 | AAAGCAAAGAAAAAA[C/T]CCTAGGCAAACACAA | 17420 |
rs49876510 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73224124 | CTGTTTAGTCTAGAG[C/T]AAATGCTCACGAGAC | 17420 |
rs49890774 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73178099 | AATGAATTTCATCTA[G/T]CCATATACATTTCAC | 17420 |
rs49907999 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73190149 | CATGAACATGTTTTT[A/C]TATTAAGGCCTTCAG | 17420 |
rs49910457 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Mnat1 | Mm_Celera | 12:73170925 | GATGTGTGTGCATGT[A/G]TCAGCTCTACCCAAG | 17420 |
rs49912219 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73162024 | TATTTTGAAATGCCA[A/G]TATTTTGTCTTTAAT | 17420 |
rs49914477 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73247485 | GTGACCATTGGCTAT[A/G]TTTAGAGATTTTGTC | 17420 |
rs49942808 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73228473 | TGAGCTGAGAACAAG[A/G]TTCCGAGTTAAGCAT | 17420 |
rs49989728 | snp | G/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73157699 | GTGAGTACTTCTACA[G/T]CTCTTCCAGGTGAAG | 17420 |
rs49991511 | snp | A/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73207161 | TGGTGATTTTATCGA[A/T]GCAACAGGCAGCCGT | 17420 |
rs49994421 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73242396 | GATCTTAGATGAGTA[G/T]TAAGTGTTATGATTG | 17420 |
rs49996130 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73130593 | AGCACCTGCTGCACA[C/T]TGTAAATGTGTCCCT | 17420 |
rs50002607 | snp | C/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73118412 | TCGAATGGGCTTAAG[C/T]GAGAGGACTACTTGC | 17420 |
rs50022664 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73233547 | AAAAGTTTGACAAGT[A/T]CAGATGCTCTAATCA | 17420 |
rs50050182 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73217999 | TTTCACCAGCCTTTT[G/T]CCATAACACACCTGT | 17420 |
rs50056959 | snp | A/G | 0.32 | 0.24 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73271306 | ATTATGTTAGAAATA[A/G]GAAGTTGCTCATGCA | 17420 |
rs50068596 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73151704 | GTCGGGTACTCTTAC[C/T]AACTGAGCCATCTCA | 17420 |
rs50090368 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73217448 | GGCACCACTGAGGTA[C/T]TGCACCATGTGAGGT | 17420 |
rs50102952 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73191954 | agggaaaattaaaga[C/G]tttttgcagggccat | 17420 |
rs50130957 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73159656 | CAGCACATTTATTTA[C/T]TGAGTTTACACATTT | 17420 |
rs50143306 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73157748 | CTATAGGAACTCCCT[A/G]ATAGAACAGAACTAG | 17420 |
rs50168048 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | GRCm38.p3 | 12:73190024 | ACAGATCCATAGCTT[C/G]TTGTGAATTGGTTTT | 17420 |
rs50171761 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Mnat1 | Mm_Celera | 12:73168304 | GTGTTTTACAGCATT[G/T]TTTGAGTTTATAGAG | 17420 |
rs50224087 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269822 | TCAACTTTAACAATA[C/T]TTGCTCACTGCATTG | 17420 |
rs50232745 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Mnat1 | Mm_Celera | 12:73188709 | CTTTTCTCCTGACAG[A/T]TTTTTTCTATACAAA | 17420 |
rs50233339 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73206157 | TTAAGAGTGCTACTG[C/T]TTCGAATGTATGTTA | 17420 |
rs50247965 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73201836 | TCTCTGCTGTCAGAA[G/T]CATGTCTTATGAAAC | 17420 |
rs50250295 | snp | C/T | 0.18 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73164770 | TATGTTGTTTGAACA[C/T]TAATGGCATTCTTTT | 17420 |
rs50257464 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73205073 | TTTTCAAGTTGTAAT[A/G]CCCATAAAATACTTA | 17420 |
rs50267304 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73118886 | TAATGCTAATAGATA[C/G]CAAACAATGTGGAGG | 17420 |
rs50324963 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Mnat1 | Mm_Celera | 12:73183698 | CAAATTAGATGTGGG[C/T]AAGAAAATAGAGGAT | 17420 |
rs50330360 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73239035 | ACCGGGGGTCCATCC[C/T]ATAATCAGCCACCAA | 17420 |
rs50331393 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Mnat1 | GRCm38.p3 | 12:73195856 | TTTATGTGATCATTT[C/T]GGGGTTGAGAATGGT | 17420 |
rs50345535 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73208209 | TGGCAGTGAAGGGTT[C/T]AAAACCTGGGTAGAG | 17420 |
rs50362374 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Mnat1 | Mm_Celera | 12:73198716 | TGGTATATCTGAATA[A/G]CTTAAATCTATTTTC | 17420 |
rs50371658 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73154354 | GAGCATGTCACGGTT[A/G]TATTTACAAGTAACC | 17420 |
rs50373996 | snp | C/T | 0.42 | 0.183303 | intron-variant | Mnat1 | Mm_Celera | 12:73167568 | CATTGGGAAGCAAGC[C/T]ATTCCTCATTTCTTC | 17420 |
rs50383484 | snp | A/G | 0.18 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73164769 | TTATGTTGTTTGAAC[A/G]TTAATGGCATTCTTT | 17420 |
rs50384234 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73241192 | TAACTTTTTAAACTG[A/T]GGAGAAATTAATAAG | 17420 |
rs50390092 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73249478 | AGCTTCATGTGGTCA[C/T]TCACTAGAAGCAGTA | 17420 |
rs50390674 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73157630 | AAGTACATGCTTTTA[A/G]CCACTGAACCACCTC | 17420 |
rs50394697 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Mnat1 | Mm_Celera | 12:73238125 | TATTGGGTACAGGAA[A/G]GAAGGGTGACTGAGT | 17420 |
rs50411185 | snp | C/T | 0.18 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73265622 | ATTAATGTCTATTTA[C/T]GTAAGAGTCGGGGAG | 17420 |
rs50422006 | snp | A/G | | | upstream-variant-2KB, intron-variant | Mnat1 | Mm_Celera | 12:73122441 | CTGTCACCCTGTCTC[A/G]AAAAACAAAATAAAC | 17420 |
rs50424514 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73117531 | TAAAGTCACCCCTTT[C/T]CGTTGCTACTTAACG | 17420 |
rs50435973 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Mnat1 | Mm_Celera | 12:73246342 | CTGCAAGAGAAAAAG[G/T]GTCTTTCCTTCTCTC | 17420 |
rs50455275 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73241945 | GCTGGCTTCAGGAAA[A/C]GGTGTGGCAAGGAAG | 17420 |
rs50459382 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73215146 | ACATGCCTTTAATCC[C/T]AGCACTTGGGAGGCA | 17420 |
rs50474572 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Mnat1 | Mm_Celera | 12:73267002 | TACATTCAGAACACC[A/G]TAGTGCCCAATTCTT | 17420 |
rs50477592 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73145415 | AGGAGTTCTATGACC[C/T]GCTTGGGCATTTTGG | 17420 |
rs50481074 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Mnat1 | Mm_Celera | 12:73220995 | ATAAATAATAGAAGT[A/G]CATTGTTGGATTTAT | 17420 |
rs50486181 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Mnat1 | Mm_Celera | 12:73267258 | TAGTTTACTTCAGCT[A/G]ATGTTAGAATCTGTG | 17420 |
rs50503718 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73203443 | GGGACATACAGGGCC[C/T]AAGAAAGGCATTAGG | 17420 |
rs50563035 | snp | A/G | 0.18 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73171229 | TAGGGGTTGATGTTT[A/G]TTTCATTTTTGCTAA | 17420 |
rs50564181 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73212181 | AGGATTTTTTTCTTA[A/T]TTTTTCTATGATTTA | 17420 |
rs50566413 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73214391 | ATCCAAGACTTGCTA[C/T]GGTGGGAGAATTGGG | 17420 |
rs50590306 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73270871 | GCATCCTCAGAGGCG[A/G]GTAGCATGGCATGAT | 17420 |
rs50593508 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73155105 | TTGGTCTTTATAAAT[A/G]ATGTGACCTACTGAA | 17420 |
rs50600875 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73227811 | ACTACGCTAAGGGAG[G/T]AGGCTCACTTTGTAG | 17420 |
rs50632106 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Mnat1 | Mm_Celera | 12:73195515 | ACAATCACTAATTAG[C/T]AAATGTAATAAATGC | 17420 |
rs50635158 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73207526 | TTATGCTGAGCGATA[C/T]GTAGGCTTTCAGAGG | 17420 |
rs50639056 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73168418 | TGATGTAGAAAATAG[C/T]GATAATCCTTCTTCT | 17420 |
rs50646729 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73195740 | TGGCTTTGGCCAGCA[A/G]TATTGAAGACTGTCA | 17420 |
rs50690257 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73270852 | ACAGTTTCTGAAGTC[A/G]GATGCATCCTCAGAG | 17420 |
rs50701646 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73251972 | ACAGGAAGGTTGATT[A/G]GGCATGTTAATGCTT | 17420 |
rs50707130 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73219794 | ATTAAAATTAACAAC[A/G]ATAGCAGCAGAGATA | 17420 |
rs50721271 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73158539 | ATGTACTTTTGCATA[C/T]GTTAAGACCTTTTAC | 17420 |
rs50741485 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Mnat1 | Mm_Celera | 12:73170899 | AGAGGAAGCATTCTT[G/T]AGCTGGGATGGATGT | 17420 |
rs50790582 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269096 | ATTTTTTAAAAAATT[A/G]AATTTAGTCTGTTTT | 17420 |
rs50806655 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73188420 | GACACATGTAGTGTA[A/G]AGAGAGTGGAAAGCA | 17420 |
rs50835391 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73225351 | TTTCTCTCCTTGTCC[C/T]TGCCTCCTTCTGTCT | 17420 |
rs50853288 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73246747 | CCTCTCTCTCATTTT[C/T]TCTTCGATCACTAGT | 17420 |
rs50853479 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73241744 | GTGGGGAGCTTAAAG[C/T]TGACATGTTGGGTAG | 17420 |
rs50853531 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73209106 | AATAACAATGTCTTC[C/T]TGAAAATTACTCTTA | 17420 |
rs50869922 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73117361 | AGCTCTCTCTTTCTA[C/T]GTATACATGAATTCC | 17420 |
rs50890302 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73231939 | AATGCATTTCCATTT[A/G]AAGAGACTAAAGAAA | 17420 |
rs50919637 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73208189 | AGATACATGCTTAGT[A/G]TCTTTGGCAGTGAAG | 17420 |
rs50950546 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73124079 | AAAAGGTTCGTAGCC[G/T]CTCGCCCCTATCTTT | 17420 |
rs50965923 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73172017 | GCAGCATTAGGACAC[C/T]GACTGAGAAGATGCT | 17420 |
rs50974240 | snp | C/G | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73273358 | GATGTAGTTTTCCAC[C/G]CACCAAAGCTTCAAG | 17420 |
rs50991800 | snp | A/G | | | intron-variant, upstream-variant-2KB | Six4, Mnat1 | Mm_Celera | 12:73111782 | CCCATCTGAGCCACT[A/G]GTCTCCATTAACTCT | 17420 |
rs50996991 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73206343 | TAGACTTGGCTATAT[A/G]TGAAGGATAAATGTT | 17420 |
rs50997975 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73248617 | GCCTGTTTGTTCTGA[A/G]TATTTTATGTAGATA | 17420 |
rs51011052 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73197642 | TGCGGGGCCCTTCTC[A/G]CTTACATGGTGGTTA | 17420 |
rs51032238 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Mnat1 | Mm_Celera | 12:73181961 | CTTAGAGACTAAGCT[C/T]CCAGGGACTCTGCAG | 17420 |
rs51080111 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73256453 | TCAGATGGACCATTG[C/G]ACTGGGACTTGATCT | 17420 |
rs51086507 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Mnat1 | Mm_Celera | 12:73185277 | AAAGGCCTTCAGGCT[C/T]CAGCATTTAGAGTGC | 17420 |
rs51098061 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73203220 | CAAACTGGCTTGTCT[C/T]CCATCCTGGAGTCAC | 17420 |
rs51108268 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73245609 | CAATATCACTGTTCA[A/G]TCTTAAAATGTCCGT | 17420 |
rs51110478 | snp | C/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73151121 | TCGAATTGCTTATTG[C/T]CAAAACAAAGAAGTG | 17420 |
rs51114388 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Mnat1 | Mm_Celera | 12:73170983 | TTGACTTGGTAGAAG[G/T]TCTTTTAACTCTGTC | 17420 |
rs51124811 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73239086 | GACAAAGTTTGGAGC[A/T]AAGACGAAAGGATGG | 17420 |
rs51135045 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Mnat1 | Mm_Celera | 12:73182001 | AACAGCAGTTCAGAG[G/T]GTTCCTGCTCTAGTT | 17420 |
rs51139697 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73159395 | CATTAAAATTTCTGG[A/G]TTCAAGTTTCTACTC | 17420 |
rs51147549 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73227908 | ACTTTAAGTGTTAAG[C/T]AGAGTAATACTTAGA | 17420 |
rs51151395 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Mnat1 | Mm_Celera | 12:73155073 | AAAAGCTTTGCTTAA[C/T]CTGTTATCATTTTGT | 17420 |
rs51155876 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73204046 | ACTGATAATAAAGGG[C/T]ATTTTGTTGCCACTT | 17420 |
rs51181197 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73248707 | AGAACTCCATTTTTT[G/T]TAGATCAAATAATAT | 17420 |
rs51187981 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Mnat1 | Mm_Celera | 12:73169386 | AAGTTAAATGAGGGA[C/T]GAAGAGAAAGAAGGT | 17420 |
rs51199229 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73142144 | AGCTGGGCAGTGGTG[A/G]TGCACGCCTTTAATC | 17420 |
rs51212483 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73125985 | CAGCCGCACAAACTT[C/T]CCCACACTTGCTCTC | 17420 |
rs51222603 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | GRCm38.p3 | 12:73249713 | TGATCTCTTATACTT[A/G]TTTTGTTTAACTAAA | 17420 |
rs51226548 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73146189 | TTTTAAGTAACACTG[C/T]TTTATGCATAACACT | 17420 |
rs51229641 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73215107 | TCATTACTTTAAGAA[G/T]GTATTTTATAGGCCG | 17420 |
rs51266809 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Mnat1 | Mm_Celera | 12:73196527 | TTATGAGACATGATG[A/G]TCAAGGGACAGAAAA | 17420 |
rs51284345 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73224473 | TTTTAGTCTTTTCAG[A/G]GTTTTAAGAAACTGA | 17420 |
rs51286010 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Mnat1 | Mm_Celera | 12:73167656 | TTTATAACTGGTATC[C/T]TCTCAGTTGTCTGAA | 17420 |
rs51293938 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73238822 | GTACTGGTTAGTTCA[C/T]ATTGTGTTCCACCTA | 17420 |
rs51313053 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73242421 | TGATTGTGGAGTTGT[A/G]ACAAACCCAATGTCA | 17420 |
rs51314735 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73239115 | AATAAAATATCCATG[A/G]AAGGAGTTGCAGAGA | 17420 |
rs51319599 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73159715 | TAGATTTGATTGTCT[C/G]TCTACTGCCAATACT | 17420 |
rs51342874 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73251743 | CATCTTTACATGGAG[C/T]CACCTTTCTGACCCC | 17420 |
rs51356219 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73229065 | CACCAGGAAGACCCA[C/G]CACTGTGCTTTCTGA | 17420 |
rs51399213 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73274486 | TAAATGATGGTCAAT[A/G]GATGATCTCATTGAT | 17420 |
rs51421161 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73216583 | TCAAACTGAACAGTG[C/T]GTGGTTTGTCCCCAA | 17420 |
rs51423948 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73166933 | TACTTTGTAATATTT[C/T]ATGATTCCTTTCTTC | 17420 |
rs51429421 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73236988 | ACCGCGACTACTGAA[C/T]GCCAAAAATCAAAAA | 17420 |
rs51443716 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73226371 | GTAAAATAAATTGCT[A/C]CTTGTGGTATGAACA | 17420 |
rs51451898 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Mnat1 | Mm_Celera | 12:73184547 | TTGGCACCTGTAAGT[A/C]TGTCTAAAAGGGTCA | 17420 |
rs51479090 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73226205 | CCACATGCCCAGCCT[A/G]TCTCCATGATTAAGA | 17420 |
rs51484257 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73273447 | GCATCCCAGCCTGTG[C/T]GAGTCTGTCGCATGG | 17420 |
rs51503191 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73214474 | CCTCCCGCCATCTGA[A/T]TATCTCCAGTGCTAC | 17420 |
rs51527072 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73253060 | TAGATTTTGTCAAAG[G/T]CTTTTTCAGCATCTA | 17420 |
rs51542397 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Mnat1 | Mm_Celera | 12:73240639 | TAGGAAGTTGCCCTC[C/T]TTGAAGATGGTTTTG | 17420 |
rs51561464 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73269155 | ATAAGCAATCCCACA[C/T]TGGTTTCTATGTATA | 17420 |
rs51564747 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Mnat1 | Mm_Celera | 12:73185905 | ACCAAGCAGAGGTCC[A/T]TAGGCTCGACAGGTA | 17420 |
rs51570551 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73203988 | TTGAATGACAATATG[A/G]CATGAAAGACCCTCC | 17420 |
rs51575471 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Mnat1 | Mm_Celera | 12:73123700 | TGGCTTCCAGCCGGT[A/G]CTCTTTCGCGAAGGA | 17420 |
rs51580287 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73142897 | ACTCTAGTTGGGTAG[C/G]TTGAGGAATCTTAAA | 17420 |
rs51599511 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73271318 | ATAGGAAGTTGCTCA[A/T]GCATTAAGATCTTGA | 17420 |
rs51613821 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Mnat1 | Mm_Celera | 12:73188226 | GCTCGAGAAGCCCAG[A/G]TCCATGAAGCCAGTG | 17420 |
rs51658051 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73188652 | TATATTTAGGGAACA[A/T]TTTATCTACTGGTGT | 17420 |
rs51676031 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73146135 | GTAGGTATCCTTAAT[C/G]TTGGCTATATAATCA | 17420 |
rs51683574 | snp | C/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73204570 | CTCATGGAACCATTT[C/T]CCCAGTCAAAAGTCT | 17420 |
rs51691946 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73145553 | GTGGTTGTCTTGGGC[G/T]CATTCCTTACCCAGT | 17420 |
rs51716285 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Mnat1 | Mm_Celera | 12:73169277 | TTTTTTAAACTGAAA[A/G]TGGCAAATTCTTCCT | 17420 |
rs51716480 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73241872 | AAGTCTAAGCACTAA[A/G]CACAGGCCTGAGAGG | 17420 |
rs51728801 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73249443 | CTTCTCTCCAGGCTA[A/G]AGTGCCCTTTCCTTG | 17420 |
rs51739300 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73246629 | TCCCACTCTATTCCT[A/G]TTACTGGCTGATAGT | 17420 |
rs51796481 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73271730 | TAGGCTCTGTCCCAC[A/G]CTTCTTAGACGTGTA | 17420 |
rs51812321 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73235235 | TCATCTGCAATATCT[C/G]TTTAAATAAAAATGC | 17420 |
rs51898426 | snp | A/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73187996 | GCAGTCTTTTTTTTT[A/T]TTACAGAATGTTAAT | 17420 |
rs51910527 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73241203 | ACTGTGGAGAAATTA[A/G]TAAGTATAGTGGATA | 17420 |
rs51921692 | snp | A/C | 0.375 | 0.216506 | intron-variant | Mnat1 | Mm_Celera | 12:73259601 | AGATTTTTTTCCACG[A/C]TCACCAATGTTTTGG | 17420 |
rs51941956 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73245619 | GTTCAGTCTTAAAAT[G/T]TCCGTTTCTCTTGTG | 17420 |
rs51947228 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73130504 | TGTACTATGTCATAA[A/G]AGAGTCCCAGGAACA | 17420 |
rs51976431 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73151909 | ATCAAACACTTAAGT[C/T]GTACAGTGTTGTTGT | 17420 |
rs51981679 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mnat1 | Mm_Celera | 12:73230457 | CTTGGGCCAGAACAT[A/G]AGACTGTCTTTTCCC | 17420 |
rs51986909 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73270799 | GTCCAGCTCCTGTGA[G/T]ACTTAAGGCTCTACC | 17420 |
rs52032720 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Mnat1 | Mm_Celera | 12:73163984 | AGCGTAACTGACGTA[A/T]TCAGGTATTTTTTCT | 17420 |
rs52050320 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mnat1 | Mm_Celera | 12:73164801 | CTCGGTAAAATCAGA[A/G]AGAGAAAGGCTGGGT | 17420 |
rs52087351 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73186896 | AGGAATAAAGAAAGG[C/T]AATTTAAAAAAATTA | 17420 |
rs52095297 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73161113 | tatttatttatttat[G/T]tatgtatttatttat | 17420 |
rs52096125 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73167204 | GAGGGAGGGAGGGAG[A/G]GAGGGAGAGAAGGAG | 17420 |
rs52099667 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73237986 | AGACAGACAGACACA[C/T]ACATACATACATACA | 17420 |
rs52107876 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73170145 | CAGAGTGAGTTCCAG[A/G]ACAGCCAGGGCTACA | 17420 |
rs52176547 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73237984 | ACAGACAGACAGACA[C/G]ATACATACATACATA | 17420 |
rs52179089 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73237966 | AGATAGATAGACAGA[C/T]AGACAGACAGACAGA | 17420 |
rs52306683 | snp | A/T | | | intron-variant | Mnat1 | GRCm38.p3 | 12:73173769 | AAATAAATAAATCTT[A/T]AAAAAAAAAAAAAAA | 17420 |
rs52345444 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73215214 | CTACAGAGTGAGTTC[C/T]AGGACAACCAGGGCT | 17420 |
rs52352697 | snp | C/T | | | upstream-variant-2KB, intron-variant | Mnat1 | Mm_Celera | 12:73122573 | TGCCTTTTTCTCTCT[C/T]TCTTTCTTTCTTTCT | 17420 |
rs52362309 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73170239 | AGAGAGAGAGAGAGA[G/T]AGAGATTTGTGCATG | 17420 |
rs52380543 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Mnat1 | Mm_Celera | 12:73238051 | GACCATACAGAGAAA[A/T]CAATAATCTGAATGG | 17420 |
rs52388591 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73167192 | GAGGGAGGGAGGGAG[A/G]GAGGGAGGGAGGGAG | 17420 |
rs52401901 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Six4, Mnat1 | Mm_Celera | 12:73114713 | AATTTGGTGAGGTTT[G/T]CTTTCTTCCCATTTC | 17420 |
rs52401925 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73167215 | GGAGGGAGGGAGAGA[A/T]GGAGGGAGAGAAGGA | 17420 |
rs52434040 | snp | A/G | | | intron-variant | Mnat1 | GRCm38.p3 | 12:73173762 | ATATAATAAATAAAT[A/G]AATCTTTAAAAAAAA | 17420 |
rs52472415 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73237962 | AGATAGATAGATAGA[C/T]AGACAGACAGACAGA | 17420 |
rs52475290 | snp | A/G | | | intron-variant | Mnat1 | GRCm38.p3 | 12:73173745 | AGCTACAGTGTACTT[A/G]CATATAATAAATAAA | 17420 |
rs52493644 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73156817 | CTGTTTCTTTCTTTT[C/T]TTTTTTTTTTTTAAA | 17420 |
rs52519186 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73167195 | GGAGGGAGGGAGGGA[A/G]GGAGGGAGGGAGGGA | 17420 |
rs52583391 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73227616 | TGGAAGAACTTGGGT[A/G]AGGGGAAGAATATGA | 17420 |
rs52585068 | snp | C/G | | | intron-variant | Mnat1 | GRCm38.p3 | 12:73204262 | TCTGTTTTGCTCTCT[C/G]TCTCTCTCTCTCTCT | 17420 |
rs52606939 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Mnat1 | Mm_Celera | 12:73171533 | ATGAATGAATGTAAA[A/G]CACACATTAAGTAAA | 17420 |
rs52612069 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Mnat1 | GRCm38.p3 | 12:73151492 | ATTCTCAACTTGTTG[C/T]TTGGCATGGAAAATG | 17420 |
rs52615265 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mnat1 | Mm_Celera | 12:73127967 | GAAGAAATCAAAAGC[A/G]TGAAATCTGCAGCCA | 17420 |
rs52618359 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mnat1 | GRCm38.p3 | 12:73151488 | AAGAATTCTCAACTT[A/G]TTGTTTGGCATGGAA | 17420 |
rs52622238 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mnat1 | Mm_Celera | 12:73211973 | ATCAAATCAATAAAC[A/G]TTTCCAAGACCTTAA | 17420 |
rs52622679 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Mnat1 | Mm_Celera | 12:73211972 | AATCAAATCAATAAA[C/T]GTTTCCAAGACCTTA | 17420 |
rs52623497 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73218688 | TGTGGTTTGTGATGG[C/T]AATACACTATACTCA | 17420 |
rs52643624 | snp | C/G | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73149192 | TGTTATAGTAATCAT[C/G]TTCTTTTGTGTTACA | 17420 |
rs52643754 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73225639 | TGACTCTGTCCTTTT[C/T]TTGACTCTGAAAGTG | 17420 |
rs52646781 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mnat1 | Mm_Celera | 12:73227557 | TTCTTGTTCATTTTT[C/T]GAGAAAGATCTTAAG | 17420 |
rs52651643 | snp | C/T | 0.32 | 0.24 | intron-variant | Mnat1 | Mm_Celera | 12:73237534 | CCGGAGCAGTGGCTT[C/T]AGATTTAAGCGCACT | 17420 |
rs52651743 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Mnat1 | Mm_Celera | 12:73170373 | TTTGTGAACAGAAAT[C/G]AACCTTCCACACCCT | 17420 |
rs108311684 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73239081 | ATGGTCCATCCTTTC[A/G]TCTTAGCTCCAAACT | 17420 |
rs108572319 | snp | C/T | | | intron-variant | Mnat1 | GRCm38.p3 | 12:73186092 | ACACACACACACACA[C/T]ACACACACACACACA | 17420 |
rs108647456 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73239127 | CTTAGAATAGGGAAC[A/T]AAATACCCATAGAAG | 17420 |
rs211703523 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73235297 | GCTCTATCATTAAAC[A/G]TGCTTATCTAGTGCA | 17420 |
rs211753830 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73181593 | GGTTTGGTGTCGGTT[C/T]TCCCCTAGGATAGTA | 17420 |
rs211807571 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73173852 | CAGCTCAGTTATGCA[C/T]CATAAATTATTTGTA | 17420 |
rs211815155 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73172945 | ATTTCCTGTCTCTGA[A/G]TCTCAGTGCTGGGGT | 17420 |
rs211837456 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73226106 | GGTGATGGTAGTACA[G/T]ACTTGAGTCATGGCA | 17420 |
rs211838115 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73162884 | AGGAAATGCAGCATC[C/T]GTTCTCAGCCTCACT | 17420 |
rs211838207 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73147921 | TAGCTCAGTGTAATA[A/G]TACTTGCCTAATATG | 17420 |
rs211854212 | in-del | -/TT | | | intron-variant | Mnat1 | Mm_Celera | 12:73227881 | TCAAAATGGGTTTTG[-/TT]TTTTTTATATAACTT | 17420 |
rs211870861 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73218503 | TAGTTAGAACTTTAA[A/T]ACAAAACAAAACACC | 17420 |
rs211875278 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73226519 | CCTCTCACTTTCCAC[C/T]GTCATTGGACTGTAA | 17420 |
rs211877156 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73162134 | AATTCTGGTTCTGAC[C/T]GACTCATTGATTAGT | 17420 |
rs211907217 | in-del | -/CCAG | | | intron-variant | Mnat1 | Mm_Celera | 12:73226760 | AAATACCCTTTGGCT[-/CCAG]CCAAACTGATTGATA | 17420 |
rs211936299 | in-del | -/TATG | | | intron-variant, upstream-variant-2KB | Six4, Mnat1 | Mm_Celera | 12:73110688 | GAGCATGGCTCAGGA[-/TATG]TGTGTGTGTGTGTGT | 17420 |
rs211958437 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73190983 | AACCCATGGCGGCTT[C/T]TCCCTCTCGTAGTTC | 17420 |
rs211972692 | in-del | -/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73211253 | TACATTTACCACGGT[-/G]GGAGGAGCTGGTTAC | 17420 |
rs211972927 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73253019 | CTATTACTACTCTCT[C/T]GTGGACTTTTATCAT | 17420 |
rs211980072 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73266804 | GAAGCAGGTGGCTGA[A/G]AGATCAGATTCTCTC | 17420 |
rs211985875 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73180931 | AAAAATAAAGTTATA[C/T]TTATTAGTACCAGGA | 17420 |
rs211988485 | snp | C/T | | | upstream-variant-2KB, intron-variant | Mnat1 | Mm_Celera | 12:73122140 | CATTAAAAATGTCCA[C/T]ATTTCACTGTTATTT | 17420 |
rs211999033 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73192295 | AAGGTGTCACACAGA[A/G]CAGCTGAGGCTCAGC | 17420 |
rs212010174 | snp | C/T | | | intron-variant, upstream-variant-2KB | Six4, Mnat1 | Mm_Celera | 12:73111918 | CGCGGAGGCAGGGAC[C/T]CCGGCCGGCGCCGGC | 17420 |
rs212013595 | in-del | -/C | | | intron-variant | Mnat1 | GRCm38.p3 | 12:73253906 | AGTCATTCATTTGTG[-/C]CCCCCCCCCTTTTTT | 17420 |
rs212034899 | in-del | -/CCCCC | | | intron-variant | Mnat1 | Mm_Celera | 12:73119617 | CACCATCATCATCAT[-/CCCCC]CCCCACCACCACCGT | 17420 |
rs212050900 | snp | C/G | | | intron-variant, upstream-variant-2KB | Six4, Mnat1 | GRCm38.p3 | 12:73111119 | GCTTCCATGGCTCCC[C/G]GGTTCCTTCCCAGAG | 17420 |
rs212055219 | snp | C/T | | | upstream-variant-2KB, intron-variant | Mnat1 | Mm_Celera | 12:73123060 | GCCTTTGTGTAGGAA[C/T]AGGTACTAGATATTA | 17420 |
rs212077121 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73145097 | TCTGCACAGTCCTCA[A/G]GCATCAACATGTCTC | 17420 |
rs212079417 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73217157 | CAGGGGGACTGGGTG[C/G]ATGGACTGGAGAATG | 17420 |
rs212105218 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73160453 | TCTGGCACTCAGAGG[A/G]GCCTCTGGAATGTCT | 17420 |
rs212107345 | snp | A/C | | | intron-variant | Mnat1 | Mm_Celera | 12:73210377 | TTCCAGTCTCCCCCC[A/C]ACCTCATTATAGATA | 17420 |
rs212111557 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73225339 | CTGAATGTAATTTTT[C/T]TCTCCTTGTCCCTGC | 17420 |
rs212169120 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73253963 | CTATAAATTTCCTTA[A/G]TAGGGTGACTTTCAT | 17420 |
rs212179245 | in-del | -/TGAAGGAGGAC | | | intron-variant | Mnat1 | Mm_Celera | 12:73117966 | GACCACTCTCATTGA[-/TGAAGGAGGAC]TGATCCAAAATCATA | 17420 |
rs212219794 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73133173 | GGGCGTGGTGGCGCA[C/T]GCCTTTACTTCCAGC | 17420 |
rs212226561 | in-del | -/GCAGAGG | | | intron-variant | Mnat1 | Mm_Celera | 12:73127569 | ACTTGGGAGGCAGAA[-/GCAGAGG]GCAGAGGGCAGAGGC | 17420 |
rs212228825 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73245003 | CCAGCCTTGCCTGTT[A/G]GGAGGGGCAGTGAGA | 17420 |
rs212241290 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Six4, Mnat1 | GRCm38.p3 | 12:73114241 | acacacacacacaca[C/T]acacacacacacaca | 17420 |
rs212260432 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73265410 | GCAGACACAACAGGA[C/G]TAAGTGTGTAGAAAG | 17420 |
rs212268314 | in-del | -/ACCTGCCTCT | | | intron-variant | Mnat1 | Mm_Celera | 12:73161239 | CGAACTCAGAAATCC[-/ACCTGCCTCT]GCCTGCTAAGTACTG | 17420 |
rs212285251 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73179178 | AAAACTATTAAAGTT[C/G]ATGACATTGTTTCCT | 17420 |
rs212382932 | in-del | -/TGCT | | | intron-variant | Mnat1 | Mm_Celera | 12:73255648 | TTGAATTCTGTCTTC[-/TGCT]TGCTTGATCCATCCT | 17420 |
rs212408521 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73170770 | TGATGGATTTTGATG[A/T]GGTAGTGGTTGCCAA | 17420 |
rs212418942 | in-del | -/T | | | intron-variant | Mnat1 | GRCm38.p3 | 12:73248555 | AAGGCTTCTCTCCAG[-/T]TTTTTTTTTTTTGCT | 17420 |
rs212442126 | snp | A/C | | | intron-variant | Mnat1 | Mm_Celera | 12:73159084 | GAAGCATAGAGAGTT[A/C]ATTGGGAGATGGCTC | 17420 |
rs212447034 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73232449 | CATTATTGAAAAACT[A/G]AGATATAAGTAGGTA | 17420 |
rs212447806 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73134285 | CTTATGCTTTGTCTC[C/T]CTCAGTGCCTGCGCA | 17420 |
rs212484824 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73224918 | GCTGGAGGTGGAGGG[C/G]ATACAGGGAGTCCCA | 17420 |
rs212516479 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73211408 | CAGTAGGTGTTCCTA[A/G]CCTCTGTACCATCTC | 17420 |
rs212535906 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73209200 | GCAAATACTGTATTT[A/T]AAAAAAAAATTAGCA | 17420 |
rs212542940 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73242761 | TTTATGATTCACTGC[G/T]TTTAGAAGATCAAAT | 17420 |
rs212575711 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73251189 | ATGCTATGCTGCTTA[C/G]GTGTGCATCAGAGTG | 17420 |
rs212577710 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73189773 | TGAGGATTGAATAAT[A/G]TGTTCCTTAACTGCT | 17420 |
rs212585671 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73262321 | ATTTCTTCCTTGACC[A/G]AAATATCATTGAGTA | 17420 |
rs212593103 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73118413 | CGAATGGGCTTAAGC[A/G]AGAGGACTACTTGCT | 17420 |
rs212625040 | in-del | -/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73182697 | TATAGAATACATTAA[-/T]TTAATACCCAATTTC | 17420 |
rs212642987 | in-del | -/AC | | | intron-variant | Mnat1 | Mm_Celera | 12:73243659 | TACTTAAAAAAAAAA[-/AC]CAAAACACCAAATCA | 17420 |
rs212656805 | snp | A/C | | | intron-variant | Mnat1 | Mm_Celera | 12:73119625 | ATCATCATCCCCACC[A/C]CCACCGTCTTCATCA | 17420 |
rs212668063 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73222433 | CATATTGTTGTGTAA[C/T]CCATTATCTGTACTA | 17420 |
rs212673346 | in-del | -/TTT | | | intron-variant | Mnat1 | Mm_Celera | 12:73259881 | TGTGCAATCTTTAGC[-/TTT]TTTTTTTTTTAACCC | 17420 |
rs212704677 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73215356 | AAGTGCTCCTAGCCT[A/G]TAACAATTGTAGTGT | 17420 |
rs212705410 | in-del | -/G | | | intron-variant | Mnat1 | GRCm38.p3 | 12:73221408 | CTCATAAATACAGGT[-/G]GGTGTGATAACCCAC | 17420 |
rs212749728 | in-del | -/ACACACACAT | | | intron-variant | Mnat1 | GRCm38.p3 | 12:73186083 | TTAGTAAATACACAC[-/ACACACACAT]ACACACACACACACA | 17420 |
rs212787894 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73129357 | GTGGATTTCTGAGTT[C/T]GAGGCTAGCCTAGTC | 17420 |
rs212811938 | in-del | -/GGA | | | intron-variant | Mnat1 | Mm_Celera | 12:73238806 | ACACGAGCTCTGGGG[-/GGA]GTACTGGTTAGTTCA | 17420 |
rs212814660 | in-del | -/ATTTAC | | | intron-variant | Mnat1 | Mm_Celera | 12:73246648 | TGGCTGATAGTTTAT[-/ATTTAC]GAGTTGATTATTAGT | 17420 |
rs212828791 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73143147 | ACATAATGTGACCCA[C/T]TGCTTCAAGCTCCTG | 17420 |
rs212848453 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73260524 | GACACACCCTTAGCA[A/G]CTGTCATGTACTCTT | 17420 |
rs212893575 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73185248 | CCCATGCTTAGTTCT[G/T]TTTTAACACTCATAA | 17420 |
rs212903424 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73208627 | CTCTGTGAGTTCGAG[A/G]CCAGCCTGGTCTACA | 17420 |
rs212908827 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73240163 | TATATTGTTGCCCTG[A/G]TTGGTCTCTATCTCA | 17420 |
rs212919582 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73130613 | AATGTGTCCCTACGC[A/G]AGCTATTTCTCTTAC | 17420 |
rs212947921 | in-del | -/AC | | | intron-variant | Mnat1 | Mm_Celera | 12:73204887 | TATGTACATGAGAGA[-/AC]ACACACACACACACA | 17420 |
rs213012387 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73251932 | GGAAAAAATGCAGCA[A/G]GTAACAGGATGTTTC | 17420 |
rs213035686 | in-del | -/AATAAGTAAATGAATG | | | intron-variant | Mnat1 | Mm_Celera | 12:73171493 | ATAAGTAAATAAGTA[-/AATAAGTAAATGAATG]AATGAATGAATGAAT | 17420 |
rs213041070 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73229006 | TAGACTTGGAAAGTT[C/T]CCTGCTCTGACTTGT | 17420 |
rs213068419 | in-del | -/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73157680 | TTCTAATAGCTCTGA[-/T]TTCGTGAGTACTTCT | 17420 |
rs213071747 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73167903 | CTACCCTAGTTCTCC[C/T]TCTCTCCACCACCAT | 17420 |
rs213079864 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73229559 | CTATTTTCATAGGTG[G/T]GTGATGGTACCGTGT | 17420 |
rs213111433 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73217814 | GTGTGTGTGTGTGTA[C/T]GTACGTACGTACGTA | 17420 |
rs213122662 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73126489 | ACTTTTTGAAAAGGA[A/G]GCATGAAGTATATCT | 17420 |
rs213197545 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73259224 | AACATATGCATGGTT[G/T]CAAGGCATTGCCAGA | 17420 |
rs213208994 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73144241 | TCTGCTATTCTATCA[A/G]TAGTGGCACCTCACT | 17420 |
rs213210888 | snp | C/T | | | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73271664 | CTTTTGAGATGGGTT[C/T]GTCCTTCTGTACTTA | 17420 |
rs213219514 | in-del | -/A | | | intron-variant | Mnat1 | Mm_Celera | 12:73203489 | GCAGAGGACAAAATG[-/A]AAAAAAGAAATCAAA | 17420 |
rs213235822 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73117425 | AATCCCAGAAAGGGT[A/G]TTTCCATTTCCAAGT | 17420 |
rs213255265 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73248647 | ATAATCATAGAGTAG[A/G]TCCCTTTGTGTTTCC | 17420 |
rs213263741 | in-del | -/A | | | intron-variant | Mnat1 | Mm_Celera | 12:73119822 | ACGGAGGTTAGGGCT[-/A]AAAAAAAATTAGGCT | 17420 |
rs213275161 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73127237 | TATATTACTTATCCA[A/G]GGAAAGCTTGTGCTC | 17420 |
rs213275261 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73116833 | GAGGAAAACCAAATT[C/T]TTGTTTCAGAAAGCA | 17420 |
rs213285661 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73216252 | CTGATTTCCTTCTGG[A/G]CATGTTACTGGTATA | 17420 |
rs213288864 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73135969 | taatttggatacttt[C/T]tctgtgccctctggt | 17420 |
rs213321065 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73228271 | ACAGTTAAATGCATC[C/T]ATAAACATGTGCATA | 17420 |
rs213343503 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73214018 | TTTTGCGTTTTCTTT[G/T]ACAGTTGTGTCAATG | 17420 |
rs213368285 | in-del | -/AT | | | intron-variant | Mnat1 | Mm_Celera | 12:73209878 | TAGCTCCTTAGGACC[-/AT]ATTTGATTGCTAATG | 17420 |
rs213376589 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73165595 | GCTAATGGGAGGTCT[C/T]ATAATTGGAGATCTG | 17420 |
rs213420649 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73177577 | TCTCAAACACTTGCT[C/G]TTAGCTTCATAATAA | 17420 |
rs213428336 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73181592 | TGGTTTGGTGTCGGT[C/T]CTCCCCTAGGATAGT | 17420 |
rs213454550 | snp | A/T | | | intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73270577 | CAGGGTCTGTGTAGC[A/T]CTGGCTGTCCTGGAC | 17420 |
rs213461084 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73153297 | CTCATTAACTGCTGA[C/G]CCATCTTGTTTAGCC | 17420 |
rs213465333 | in-del | -/TTTTTTTT | | | intron-variant | Mnat1 | Mm_Celera | 12:73135321 | TTTTGGTTGGGAGAC[-/TTTTTTTT]TTTTTTTTTTTTTTT | 17420 |
rs213474752 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73140368 | TTATTTTAAAGATAG[A/G]CTTTTGTTTTATTGC | 17420 |
rs213494337 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73221924 | TAGATCTGGTATCTA[C/T]AGGTACTGAACAGAA | 17420 |
rs213555271 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73174218 | ATTTGAGTCTTTTGA[C/T]GCCTCAGAGCCTGCT | 17420 |
rs213587516 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73174950 | CACTTGTTACAACAA[A/G]GCTATATCTTTAAGC | 17420 |
rs213607943 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73195174 | AGAATTAGTCATATT[C/T]GGTTGTCATTGAGAC | 17420 |
rs213609640 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73196637 | TTCTCAGTTTGTTTC[C/T]GCCCTGTGAATTCTG | 17420 |
rs213625399 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73164399 | AGGGAGGGTCTCACC[A/G]TGGCCTTTAGTAAAG | 17420 |
rs213647077 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73182731 | TCCAAAGAGAGATAA[A/G]TGATAGAATCATGGT | 17420 |
rs213651471 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73258475 | TGTCTCTATGGAGTC[C/T]CGACCAATGCATGCG | 17420 |
rs213663976 | in-del | -/TC | | | intron-variant | Mnat1 | Mm_Celera | 12:73154618 | CAAGCAGTAATTTCA[-/TC]TGTGACCCTTTAGTC | 17420 |
rs213665363 | snp | A/C | | | upstream-variant-2KB, intron-variant | Six4, Mnat1 | Mm_Celera | 12:73115779 | ATACTTGTCCCTAAT[A/C]CTTACACCTTATAGC | 17420 |
rs213676416 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73137909 | TCTTCACTCTCTTCT[A/G]TACCTATTTTCTTTT | 17420 |
rs213688040 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73247626 | ATTACTCTTTGATTT[G/T]TGAGCTTAGTTGATA | 17420 |
rs213697024 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73202552 | TAAAAAATATCAATA[A/G]TGAAGTAACTAAACC | 17420 |
rs213700666 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73213361 | TGCTTTAGAATGAAA[C/T]GTTCTATAGATATTT | 17420 |
rs213725584 | in-del | -/TACA | | | intron-variant | Mnat1 | Mm_Celera | 12:73230159 | ACACACACACACACG[-/TACA]TGTGTGTCTTTGATG | 17420 |
rs213731442 | in-del | -/A | | | intron-variant | Mnat1 | Mm_Celera | 12:73125279 | CTTATTTTAGCTCTG[-/A]AAAAAATATTGAGAT | 17420 |
rs213771098 | in-del | -/CAGCCACAGCCA | | | intron-variant | Mnat1 | Mm_Celera | 12:73223446 | AAGGCATAGCATGCG[-/CAGCCACAGCCA]CAGCCACAGTCACAG | 17420 |
rs213775322 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73150861 | ACTTGGCAAGCTCTC[C/T]GCTTACTAATGTGTC | 17420 |
rs213779364 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73220075 | CTTTATCATCAAGGT[A/G]GGAGCAGGGTGGCAT | 17420 |
rs213832939 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73124435 | AAGAAAATACAGACT[C/T]AAGGCAGTTACTTTG | 17420 |
rs213833889 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73246126 | GGAGGGTTTACTTCA[C/T]CTTACTCCCAGGTGA | 17420 |
rs213907966 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73172548 | CAGGTTTGTGTTTAG[A/G]AGTAGGCACTAGTAT | 17420 |
rs213918830 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73254302 | GTTGAATAAAATGTG[C/T]ACTCTTTGGTGTTTA | 17420 |
rs213929414 | in-del | -/TTAATA | | | intron-variant | Mnat1 | Mm_Celera | 12:73238450 | TCCCAGCCCCCATCC[-/TTAATA]TCTTGTCTTTAATAT | 17420 |
rs213945630 | in-del | -/ACATACATACAT | | | intron-variant | Mnat1 | Mm_Celera | 12:73237983 | GACAGACAGACAGAC[-/ACATACATACAT]ACATACATACATACA | 17420 |
rs213963547 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73139418 | TAAGCCAGCACAAAC[C/T]TTTTTTGTCTATTAC | 17420 |
rs213982333 | in-del | -/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73228194 | TTCCTGGAAAAAAAA[-/T]ATGGTGGTGAATGGT | 17420 |
rs213984995 | in-del | -/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73194391 | TCTATTTTATAAACC[-/T]TTTAGGTGGTTCCCC | 17420 |
rs213988286 | in-del | -/AG | | | intron-variant | Mnat1 | Mm_Celera | 12:73210569 | TTCTGTGTGGCTGTC[-/AG]GGGTGGGGATGAATT | 17420 |
rs213991548 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73135864 | CCAGATTTTTCAGTT[A/G]TGTTGAATATGGACT | 17420 |
rs214030093 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73212695 | TAATATTTTCAACTG[C/T]TGATATTCACCAAAC | 17420 |
rs214035390 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73182223 | AGGCAAGTCAGGGCC[A/G]TTATTTGCTGAGCAA | 17420 |
rs214044305 | in-del | -/CAAAAC | | | intron-variant | Mnat1 | Mm_Celera | 12:73170430 | CAAAACAAAACAAAA[-/CAAAAC]TAAACAAAGCCAACA | 17420 |
rs214050140 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73243880 | CTTTCTAGTACAAAT[C/T]GTCTTCCTCATAGTG | 17420 |
rs214076706 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73179868 | CCTGGCCAGTTGTGG[A/G]ACACTGTCAATCTCT | 17420 |
rs214103624 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73217709 | AATAATTTTCTTGAT[A/T]GTTTACAGTAATATC | 17420 |
rs214111224 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73180850 | ATTGCAAATGAGACA[C/T]ACACACACAACTAAC | 17420 |
rs214144174 | snp | A/C | | | intron-variant | Mnat1 | Mm_Celera | 12:73160686 | TGCAGCATCGAGGCT[A/C]TAGGCTGTTCCCTTT | 17420 |
rs214145708 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73181520 | AATTAACCCAGCCCC[A/G]CCCCTGCTACCCACT | 17420 |
rs214145867 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73171246 | TTCATTTTTGCTAAA[C/G]AGAGTTCTAGAACTG | 17420 |
rs214172004 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73234482 | AGAGAAACCCTGTCT[C/T]GGAAAAACAAAAAAC | 17420 |
rs214192625 | in-del | -/TT | | | intron-variant | Mnat1 | Mm_Celera | 12:73210229 | AGAAATAAGTGCTTG[-/TT]TTTTTTTTTTTAAAT | 17420 |
rs214208211 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73235217 | GATTCAGGTTTTCCT[A/G]TTTCATCTGCAATAT | 17420 |
rs214210709 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73227459 | TGTTGTTGTTGTGTG[G/T]TTTGTTGGTTTTGTT | 17420 |
rs214227813 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73133053 | TTTTTCAGAAAGAAT[C/T]GAATTAAAGGGAAAA | 17420 |
rs214238724 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73192528 | TGACCCAAGCCCTTG[A/G]AGGAGCCCAGAAGAT | 17420 |
rs214248967 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73148554 | TGGGAATTGAACCTC[G/T]TGCATACTATGCAAG | 17420 |
rs214294339 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73211250 | TGATACATTTACCAC[C/G]GTGGGAGGAGCTGGT | 17420 |
rs214315348 | snp | G/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73218916 | ACTGAACTATCCTCC[G/T]CAAGAGCAGCGAGTA | 17420 |
rs214340739 | snp | A/G | | | intron-variant, downstream-variant-500B | Mnat1, Trmt5 | Mm_Celera | 12:73268098 | CCATAGGGTAGTGCA[A/G]TGCGCGGGATTGAAA | 17420 |
rs214344123 | in-del | -/GTGTGTGTGTGTGTGTGC | | | intron-variant | Mnat1 | Mm_Celera | 12:73165201 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGTGC]GTGTGTGTACAGGAA | 17420 |
rs214345720 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73194100 | TCTAGGCTCCTTGCC[A/G]TCAGTGGATCTCTAG | 17420 |
rs214346796 | in-del | -/TTTC | | | intron-variant | Mnat1 | Mm_Celera | 12:73126244 | ACTTTGGTATCAGAG[-/TTTC]TTTCATAGGGTTTTG | 17420 |
rs214350661 | in-del | -/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73173544 | AAAAATAAGAACACA[-/G]TAAAAAAAAACCAAC | 17420 |
rs214351933 | snp | C/T | | | upstream-variant-2KB, intron-variant | Mnat1 | Mm_Celera | 12:73121883 | ACCTGTCACCAAGCC[C/T]AATGATCTGAGTTCC | 17420 |
rs214381619 | snp | G/T | | | upstream-variant-2KB, intron-variant | Six4, Mnat1 | Mm_Celera | 12:73114855 | CCCTTCCCTTTTCCT[G/T]TTCCCTTTCCTTTTC | 17420 |
rs214389261 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73255321 | CTCTTTCAGCTTTCA[A/G]TGCTCTCCTTTGTTC | 17420 |
rs214391562 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73120847 | GGTGTCAAGCCTTGA[A/G]CCATCATGGCCTGCT | 17420 |
rs214428452 | in-del | -/CCAA | | | intron-variant | Mnat1 | Mm_Celera | 12:73142285 | AAACCAACCAAACAT[-/CCAA]CCAACCAACCAACCA | 17420 |
rs214472677 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73216491 | TGTGGAAAAAGTGAA[C/G]ACCTTTCATAGTACA | 17420 |
rs214484312 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73225918 | GTACTGAGATATTTT[A/T]AAATGATTTATTGAG | 17420 |
rs214530236 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73218301 | CATAGATTTTTAAAG[A/G]AGACTTTATGTATGT | 17420 |
rs214538708 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73225498 | AAACTTTTATTCTGT[A/G]CTTCAGGAGCTCTAT | 17420 |
rs214549369 | snp | A/G | | | downstream-variant-500B, intron-variant | Mnat1, Trmt5 | Mm_Celera | 12:73274182 | AGTACAGAAATAGCC[A/G]TTGTATGGCTTTTGT | 17420 |
rs214561326 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73133769 | gatatttgctactaa[C/T]ccaagaattcagctt | 17420 |
rs214563513 | snp | C/T | | | intron-variant | Mnat1 | GRCm38.p3 | 12:73131314 | TCCAGTCTCTTCTTC[C/T]CTTCCTTCTCCTTTC | 17420 |
rs214605678 | snp | A/C | | | intron-variant | Mnat1 | Mm_Celera | 12:73217123 | AAGAGCAATTAGAGC[A/C]CTGGCAGCAGGGGAT | 17420 |
rs214605964 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73209466 | AATAAATTCCATGGG[A/T]TCTCTCTTCCCTCCC | 17420 |
rs214628219 | in-del | -/T | | | intron-variant | Mnat1 | GRCm38.p3 | 12:73249788 | ATTCAGTAACAAATG[-/T]AAAAAGTTTATCTAT | 17420 |
rs214632458 | snp | A/C | | | intron-variant | Mnat1 | Mm_Celera | 12:73250973 | CATGGCCATCCCAAC[A/C]CAGTTTTAATGTATT | 17420 |
rs214642937 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73200505 | CTGATACAAGCTCAG[A/T]GTTCCTGGAAATGGT | 17420 |
rs214678179 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73264596 | TTTCTCAATATTGTC[C/G]GTTTCTTGCCTTATG | 17420 |
rs214680530 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73189928 | TTTATTAATATATTT[A/G]CTATGTAGAATTTTT | 17420 |
rs214686400 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73178023 | TTTCTAAGTGAAAAT[A/G]AAATAAACAGTCTGT | 17420 |
rs214718932 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73252172 | ACAACTCAGCAGTTT[C/T]CTATGTGAAGTTATC | 17420 |
rs214722267 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73168419 | GATGTAGAAAATAGC[A/G]ATAATCCTTCTTCTC | 17420 |
rs214722446 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73179039 | AGAGTCAAAGGTAGT[C/T]GTGAGTGACTTGATA | 17420 |
rs214743717 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73190941 | TCCAATTGGTCAGCC[C/T]TCAGGGCTACATTTT | 17420 |
rs214760714 | in-del | -/TTTTC | | | intron-variant | Mnat1 | Mm_Celera | 12:73127613 | TCTCTGTGATTTTTT[-/TTTTC]TTTTCCTTTTGCATA | 17420 |
rs214770792 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73241891 | AGGCCTGAGAGGATG[A/T]CTTTAGAGATTTAAA | 17420 |
rs214804366 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73213227 | TTGTTGGTATTTAAG[A/G]CCAGCCTTCATCTGT | 17420 |
rs214806639 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73157765 | TAGAACAGAACTAGC[A/T]GGTCATACTTAGTGC | 17420 |
rs214809309 | snp | A/C | | | intron-variant, upstream-variant-2KB | Six4, Mnat1 | Mm_Celera | 12:73110961 | TATGGTTACCCGCAA[A/C]AAGGGTCAGGGCTGC | 17420 |
rs214810657 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73223640 | TGTGACTTGCTTGCT[C/T]AACAACAGACAAACA | 17420 |
rs214814029 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73142978 | CTGCAGGAATCTAGA[A/G]TCACCTGGGAGCTTA | 17420 |
rs214850164 | snp | A/C | | | intron-variant | Mnat1 | Mm_Celera | 12:73215279 | ACCAAAAAAAAAAAA[A/C]AAAAAAAAACAACAA | 17420 |
rs214889475 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73208484 | TCTAGATAAGCTAGT[A/G]CTATTTGCTGGCCTC | 17420 |
rs214911035 | in-del | -/ACCCCC | | | intron-variant | Mnat1 | GRCm38.p3 | 12:73118677 | CCATAATGCAATGCT[-/ACCCCC]ACCCCCACCCCCACC | 17420 |
rs214981220 | in-del | -/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73262781 | GTTCATCTTGGTAGA[-/T]TTTTTTCCTTTGACC | 17420 |
rs214981489 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73129295 | ATTAGTGGGGCGGGG[C/T]GTGGTGGCACACGCC | 17420 |
rs214985139 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73144475 | AGCAAGCACACAATC[C/G]CAGCTAGCCCTATCT | 17420 |
rs214986123 | in-del | -/C | | | intron-variant | Mnat1 | Mm_Celera | 12:73248096 | TGGCCTCCATAGGCA[-/C]GTGAATGCACGTGGT | 17420 |
rs214996160 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73249910 | GCTCTCTTCTCCCAT[C/T]ATCCGTGGTCCAGAA | 17420 |
rs215038148 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73221141 | TCAGTTCTCTTCTTC[C/T]GCCACGTGGCTTTGA | 17420 |
rs215055203 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73200937 | GGATTAAACCTCTTA[A/G]TCCTGTGTTTTGAAT | 17420 |
rs215068150 | snp | A/C | | | intron-variant | Mnat1 | Mm_Celera | 12:73177176 | AAACAAACAAACAAA[A/C]ACATCAATGGCTACT | 17420 |
rs215068989 | in-del | -/A | | | intron-variant | Mnat1 | Mm_Celera | 12:73194154 | ATTTTATTTTATTTT[-/A]TTTATTTATTTATTT | 17420 |
rs215144781 | snp | C/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73252764 | ATGTCTCAGTCTCCT[C/G]TCCCAGTCTCCCAGG | 17420 |
rs215148526 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73141820 | GCATGCTCTCTGTCT[A/G]CCTGCCTGTCTGTCT | 17420 |
rs215159745 | in-del | -/CAACAACAGCAGCAGCAGCAGCAG | | | intron-variant, upstream-variant-2KB | Six4, Mnat1 | Mm_Celera | 12:73111238 | CAACAACAACAACAA[-/CAACAACAGCAGCAGCAGCAGCAG]CAGCAGCAGCAACAA | 17420 |
rs215200724 | snp | A/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73232244 | AAACACTAGAAATTC[A/T]TAATTTTGTATGAGC | 17420 |
rs215202969 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73214880 | TGGGAGTGTTGGAGC[A/G]CCTGGGAGTGGGTCT | 17420 |
rs215212106 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73247448 | GTCCTGCTTTGCATC[A/G]GGTCCAGGGGCAAGA | 17420 |
rs215220556 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73230551 | ACATAGCCTACCTCA[C/T]TTCCCACTAACAGCT | 17420 |
rs215223556 | in-del | -/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73253916 | TTGTGCCCCCCCCCC[-/T]TTTTTATTTTCTTAA | 17420 |
rs215246072 | snp | A/C | | | intron-variant | Mnat1 | Mm_Celera | 12:73183019 | CCTACTCCTCACTTT[A/C]CTTTTCCTCTTCTTT | 17420 |
rs215246399 | snp | A/G | | | intron-variant | Mnat1 | Mm_Celera | 12:73224817 | AGAGTGCTGGTGATA[A/G]AACTCGGAGTCTTCA | 17420 |
rs215285344 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73183849 | ATATATGCAGTCAGA[C/T]GAAATAAATAACAAT | 17420 |
rs215318681 | snp | C/T | | | intron-variant | Mnat1 | Mm_Celera | 12:73176235 | AAACAAGGTGGACAC[C/T]AGGTGGTGACGATGC | 17420 |