SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6190365 | snp | C/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140730788 | atgtagctagctgtc[C/T]ccaggtntatctgct | 23947 |
rs6190369 | snp | C/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140730795 | tagctgtcnccaggt[C/T]tatctgctgtcatcc | 23947 |
rs6190447 | snp | G/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140730836 | atgtacactggaact[G/T]tgagccaaagcaagc | 23947 |
rs6192000 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Mid2 | GRCm38.p3 | X:140731100 | AAAGGAGCTGTTGAA[A/G]GGTAAACAGTTGACA | 23947 |
rs6285993 | snp | A/G | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140670432 | TTTAAAAACAAAACA[A/G]AACAAAGAGAAACTA | 23947 |
rs6301063 | snp | A/C | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140670838 | GAAAACTTTAAGAAC[A/C]CTTTAGTAAAAGAAT | 23947 |
rs6346537 | snp | C/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140718788 | ATCCATTTTCAATTT[C/T]AATGGAATTTTGTTA | 23947 |
rs13484034 | snp | A/G | 0.457278 | 0.13977 | synonymous-codon | Mid2 | GRCm38.p3 | X:140678432 | TGAGCAGGACCCTCC[A/G]AGAGATGCTGTAAAG | 23947 |
rs29253584 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140734189 | TGAAATAGCAAGCAG[C/T]ATTACTGAATTATAT | 23947 |
rs29253585 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140734087 | TCTAGGATGCATCGT[C/T]CACTATTCTGGAGAT | 23947 |
rs29253586 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140734059 | GTTCACTCCAACAGA[C/T]ACTGACATAATGTCT | 23947 |
rs29253587 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140733987 | ATACTAACACAGAGA[A/G]CCATTTGCACATATT | 23947 |
rs29253588 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140733388 | TTGGGACTATTGAGA[A/G]TTTACATGGACTATT | 23947 |
rs29253589 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140733341 | TTACTAGAGGAACTT[C/T]AGGGAGATCCAAATG | 23947 |
rs29253590 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140733003 | CGTGACTCAGTTGGT[A/T]CTTATGCTACCTTGA | 23947 |
rs29253591 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140732570 | TTCATTAAAAAAAAA[A/G]GTCAACTGAGGACTT | 23947 |
rs29253592 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140731855 | CTTGATTTGGAGTTT[C/T]GCCTCTTCAGCCAAC | 23947 |
rs29253593 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140731256 | GGAAAACAATATGCA[A/G]GTCAAGTTCTTGCTG | 23947 |
rs29253724 | snp | A/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140763318 | TAGGAGATGGGAAGT[A/G]CTGCATCACTCTAGT | 23947 |
rs29253725 | snp | G/T | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140763298 | TTTTGGAAAATATAC[G/T]GGGCTAGGAGATGGG | 23947 |
rs29253726 | snp | A/C | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140763201 | AATTGAACAGCTAAA[A/C]AAAAATACTAGGAAG | 23947 |
rs29253727 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140762537 | TCAATGATGGATGGA[G/T]GATGGAGGATGAGAG | 23947 |
rs29253728 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mid2 | Mm_Celera | X:140762522 | AGAAGGTGAAGCTCC[C/T]CAATGATGGATGGAG | 23947 |
rs29253729 | snp | A/C | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140762300 | TGCACTCCGATTTCA[A/C]GAAAGCAAACGTCTC | 23947 |
rs29253730 | snp | C/G/T | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140762271 | CCACTCTAACAAAGT[C/G/T]ACCTAATTATATGTG | 23947 |
rs29253731 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140762220 | GAGTCTCTGAACTGA[A/C]GCACATGCTATCTTT | 23947 |
rs29253732 | snp | A/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140762206 | TCGCATGGTTATAAG[A/G]GTCTCTGAACTGAAG | 23947 |
rs29253733 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Mid2 | Mm_Celera | X:140762116 | ATAAACACACAGTGT[C/T]TATCACAGAGGCATA | 23947 |
rs29253974 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140730479 | CAGAGAGAAGGCAGA[C/T]GCACTTTAAACACAG | 23947 |
rs29253975 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140730178 | TGCAGAAACAAAAAG[G/T]TCTCCATGTGATCTT | 23947 |
rs29253976 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140730036 | ATTGTATAACTTGAG[C/T]GTTCTTTAAATTCTA | 23947 |
rs29253977 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140729917 | TGTTTAACCCCACTT[C/T]TTCATGCCCAACTGT | 23947 |
rs29253978 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140729384 | TTCACTCTGTTGCCC[A/G]GGCAATCTGATCTGC | 23947 |
rs29253979 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140728390 | TTGGGTCCTGTGCCT[A/G]TTTTCTCTCCCTACA | 23947 |
rs29253980 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140728312 | TATGGAGTGTGAGAC[A/G]AAGGAGCAAAACAGT | 23947 |
rs29253981 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140728277 | GAATGACTTCCAACT[C/T]AGGCTCTTTTGTCTG | 23947 |
rs29253982 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140728275 | GTGAATGACTTCCAA[C/T]TTAGGCTCTTTTGTC | 23947 |
rs29253983 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140728258 | ACAGAAAGCAACTGA[A/C]TGTGAATGACTTCCA | 23947 |
rs29254004 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140762036 | CTTCCTATTAACTAT[C/T]CCTAGCAGCAAGGGT | 23947 |
rs29254005 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Mid2 | Mm_Celera | X:140761771 | GTTTGTCTTTTTTTT[A/T]AACTTCCTGTCACAC | 23947 |
rs29254006 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140761699 | GCTCTTGAGCAAAAC[C/T]GACAAGAGTCCTAGC | 23947 |
rs29254007 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140761672 | CCACAGAGAAGCCAT[A/T]GTTTTAGGAGTGCTC | 23947 |
rs29254008 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Mid2 | Mm_Celera | X:140761261 | AGTTCATGGACTCCA[A/G]AGTGGGACACGCTAC | 23947 |
rs29254009 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140761174 | TACTTTTGTCTTTCC[C/T]TACTTCACAGGCCTG | 23947 |
rs29254010 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140761083 | AAGAAAATGAATTCA[C/T]GTAGGTGGTTTATAA | 23947 |
rs29254011 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140761053 | GTTCATCTCATTATA[G/T]CTTTCAAGGCTCAAA | 23947 |
rs29254012 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140760910 | ATAACTGTGAGGATT[C/T]TACTATTTGTGTTCT | 23947 |
rs29254013 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mid2 | Mm_Celera | X:140760137 | GCCAAAGAGAAAAAA[A/G]GAAGAACCCATCAGA | 23947 |
rs29254374 | snp | A/T | 0.375 | 0.216506 | intron-variant | Mid2 | Mm_Celera | X:140727585 | TTCAACAACTATTTC[A/T]CATCCATATCCTAAT | 23947 |
rs29254375 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Mid2 | Mm_Celera | X:140727504 | TCAATATCTGTCTGG[C/T]GCTCAACTCATTAGC | 23947 |
rs29254376 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mid2 | Mm_Celera | X:140718426 | CCTGGTCCGGGATGT[C/T]CCACAAAACAAAGCA | 23947 |
rs29254377 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Mid2 | GRCm38.p3 | X:140704679 | AATATGGAAAGGAAG[A/G]GGAAACAAAACAAGG | 23947 |
rs29254378 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Mid2 | GRCm38.p3 | X:140704588 | TTAGTAGGAAAGCAT[C/T]AGGCCAGGGACATTC | 23947 |
rs29254379 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140704550 | GGAATGGGGCAGCAG[A/G]CATCTGAATGCCCAA | 23947 |
rs29254380 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140704448 | CCTCAAAGAGCCATT[A/G]TACCAATTGGAGTCC | 23947 |
rs29254381 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Mid2 | GRCm38.p3 | X:140704428 | TTTAAGCCTATAAGA[C/T]TTTTCCTCAAAGAGC | 23947 |
rs29254382 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140704398 | ATCAAAGGCCCCAAA[C/T]GGTTTTGGAATAGTT | 23947 |
rs29254383 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140704373 | CCCTGTTCACCTTCT[C/T]CTCACTAAAATCAAA | 23947 |
rs29254484 | snp | A/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140760098 | ATGTTAAACCAACTG[A/G]GAAACGGATAACAGA | 23947 |
rs29254485 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140760042 | GTCCTCATTTTCCAT[G/T]CCCTTTCCTTTCCAT | 23947 |
rs29254486 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140760001 | CTCAATTCTTCATTC[A/G]AACTCTATAACAATG | 23947 |
rs29254487 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140759695 | TTTCTGTAGTACATC[C/T]TTTTGTTCCCTCATT | 23947 |
rs29254488 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140759662 | CTCCAGCCTCCTCTC[A/C]ATCAATGCTTTGTCC | 23947 |
rs29254489 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140759638 | GTTATGGGAATTAAA[C/G]AGCCATCTCTCCAGC | 23947 |
rs29254490 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Mid2 | Mm_Celera | X:140759548 | TCTCAATCAATTCTT[C/T]TTTAATTTACTTACT | 23947 |
rs29254491 | snp | A/T | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140754927 | CCAAGTCTTATTGAT[A/T]CCCACAGAATCATAT | 23947 |
rs29254492 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140754888 | TATTTTTTTTTACAT[A/T]ATTCATGTGCTGGTC | 23947 |
rs29254493 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140754850 | ATTTCCATATTTTGA[A/C]ATTTTTTGTTGACTA | 23947 |
rs29254764 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140704281 | ATGGCCTTTGTTTAT[C/T]CTAGTTTAAAGTATT | 23947 |
rs29254765 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140704266 | ACAACACTGGGAAAC[A/G]TGGCCTTTGTTTATT | 23947 |
rs29254766 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140704208 | GCTTTTCCCATGGTG[A/G]TCAATTCCTTAGCGT | 23947 |
rs29254767 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140704112 | ATGACCATTGACTGG[A/G]CATGTTAGCTACTTG | 23947 |
rs29254768 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140704047 | AGAGAATGAAAATGG[A/G]TGGTGGTGGTGAATT | 23947 |
rs29254769 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Mid2 | Mm_Celera | X:140703938 | TCTGCAAGAGTGAAT[A/G]CATGTGTGCATGTGT | 23947 |
rs29254770 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Mid2 | Mm_Celera | X:140703640 | GACCATGAAAGTACA[G/T]AAAAATAAAGTAGTC | 23947 |
rs29254771 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Mid2 | Mm_Celera | X:140703473 | ACTTGGCATTCCTTA[A/G]TCTAAGCCTCATAGA | 23947 |
rs29254772 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Mid2 | Mm_Celera | X:140703401 | CAGCTCTGGAGAGCC[C/T]ACTTTTCCCTCCGCT | 23947 |
rs29254773 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Mid2 | Mm_Celera | X:140703367 | ATCTGTTCACTGGCC[G/T]CTGATTCATAAAAGG | 23947 |
rs29254914 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140754796 | TATCTTTTCAGTAAT[A/T]CATTTGTCTCCATCA | 23947 |
rs29254915 | snp | C/T | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140754571 | AGGCAGTCTGTAGCA[C/T]ATTGCCACAAAGATA | 23947 |
rs29254916 | snp | A/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140754548 | TTAGACAGAAAGTTT[A/G]TCTAGTCAGGCAGTC | 23947 |
rs29254917 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140754404 | CCCCTGGATTCTGAG[C/T]GTTCCTATCATCTCT | 23947 |
rs29254918 | snp | A/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140753905 | GGTCTGCCGAGGATG[A/G]CCGAGCACCAGCACT | 23947 |
rs29254919 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140753880 | AAGTCCTGGTCTCCC[C/T]AGCTGGTCAGGTCTG | 23947 |
rs29254920 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140753865 | AAGAAATATCATTCC[A/G]AGTCCTGGTCTCCCC | 23947 |
rs29254921 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140753597 | TTTTCCTTACATTTG[C/T]TTTCCCTCTCAGCCT | 23947 |
rs29254922 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140753497 | GCTCAAACTCAGCAC[C/T]TTTGACTTTCTGCTT | 23947 |
rs29254923 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140753459 | CTGAGATTCCCATGT[A/G]TGATAAGTTCTGTCT | 23947 |
rs29255184 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140703051 | TCGAGACATCCTTTT[A/T]AAAAAATCTGTCTTT | 23947 |
rs29255185 | snp | C/T | 0.5 | 0 | intron-variant | Mid2 | GRCm38.p3 | X:140703037 | TGCACACACAGCTGT[C/T]GAGACATCCTTTTAA | 23947 |
rs29255186 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140702846 | AAGTCTTCACACTTT[G/T]CCCGAATTCTCCATT | 23947 |
rs29255187 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Mid2 | GRCm38.p3 | X:140702416 | TGTTCCCTATTTGTT[C/T]ACTGTCTTAGAGTTT | 23947 |
rs29255188 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Mid2 | GRCm38.p3 | X:140701750 | GTTTCAAAGGACAGG[C/G]AGTTATTTAGGATTT | 23947 |
rs29255189 | snp | C/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140701610 | CAAGAATAGCTAAGG[C/G]ATTCTTTCCATTGGC | 23947 |
rs29255190 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140701522 | CTAATGTTTTATGAT[C/T]AGTGAGCTGGCACTT | 23947 |
rs29255191 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140700907 | TACAACTCGCTTCTC[C/T]GAGACATGCTCTGTA | 23947 |
rs29255192 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Mid2 | GRCm38.p3 | X:140700817 | TGCCTCCAATCATGC[A/T]AGCTCAACCTCCCCT | 23947 |
rs29255193 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Mid2 | GRCm38.p3 | X:140700605 | AGATTGAGAGAGGTC[C/T]AGGAGAAAGCAAGCT | 23947 |
rs29255314 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140753384 | TGGGTTATATTTCTT[A/G]TACTGTACCTTTTTT | 23947 |
rs29255315 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Mid2 | Mm_Celera | X:140753082 | CTTTTAAAACATGCA[G/T]CCATCGTGTCAAAAG | 23947 |
rs29255316 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Mid2 | Mm_Celera | X:140752440 | AATGACAAGGTTATA[C/T]ACATCTTAACCTTGG | 23947 |
rs29255317 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140752257 | CTTACTTATAAGTTT[C/T]TTCTTACAGTACACT | 23947 |
rs29255318 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140752231 | GATTATGAAGTCACA[A/T]GCTCTAAGGCCTTAC | 23947 |
rs29255319 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140751702 | TGCCACAAAGTTAAA[C/G]ATGTTTAAAAGGCTG | 23947 |
rs29255320 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Mid2 | Mm_Celera | X:140750525 | TTTGCTATCTATAGA[C/T]GCATTTTTACAAGCA | 23947 |
rs29255321 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Mid2 | Mm_Celera | X:140750502 | GTAATGAGAAAGCAG[C/T]ATTTTGCTTTGCTAT | 23947 |
rs29255322 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140750347 | TGTAAATTGATTTTG[C/T]ATCATTATTCCTCAT | 23947 |
rs29255323 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140750053 | TCACATGATTCTCCT[G/T]AGCTGTTAGGACTCA | 23947 |
rs29255624 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140700549 | AGAATGTGCAGGAGA[A/G]GCAGATGTTTTGGGA | 23947 |
rs29255625 | snp | C/T | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140699443 | ATAAAAGTGAAGTTA[C/T]CTTGAAAATGAATAA | 23947 |
rs29255627 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140699260 | AGTAGAAAATGGTTC[C/T]TGCCTCCAAGGCACA | 23947 |
rs29255628 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140699167 | CTCTGGAGAGGCAGG[C/T]AGCAGTGATATTAAT | 23947 |
rs29255629 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Mid2 | Mm_Celera | X:140699075 | ATGAGTAATTACAGC[A/G]AAGTACATCCAATCA | 23947 |
rs29255630 | snp | G/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140698959 | AAGTAGTGCTATCAT[G/T]ATTTCAGCAGTAATC | 23947 |
rs29255631 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140698879 | AAGATGTGTTTGACT[A/G]GAGTCTGAACATTTC | 23947 |
rs29255633 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Mid2 | Mm_Celera | X:140697866 | TCAGAGAGTAAACAA[A/G]GTTTGAGTCTTCCTA | 23947 |
rs29255794 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140749895 | TCATGTGTACCTTTA[A/G]AAACAATTTTGTTTT | 23947 |
rs29255795 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mid2 | Mm_Celera | X:140749830 | GCTTTTTCTGGTACA[C/T]GTAGTTTTCCAGACA | 23947 |
rs29255796 | snp | G/T | 0.231111 | 0.249285 | synonymous-codon | Mid2 | Mm_Celera | X:140749683 | GAAACTATTGGAGGG[G/T]CTAGACTATTTAACA | 23947 |
rs29255797 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140749320 | AGAGGGGAAAAAATC[C/T]TGTATTTACTTCTCA | 23947 |
rs29255798 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140748819 | AGCCCTATTGCTGTG[C/T]CTTAAAGTTAGTTGG | 23947 |
rs29255799 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140748763 | TATGTGTTCAACATT[C/G]TTTTAGGAACCATAG | 23947 |
rs29255800 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140747078 | TATTCCACATGATTC[A/T]GCTTCATTCTTTACC | 23947 |
rs29255801 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140746958 | TACAGCTTTAAAACT[C/G]TCGTTAAAATATATT | 23947 |
rs29255802 | snp | A/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140746906 | AAGGCATTCAAGGGG[A/G]ATTCTCGCGTGCGAC | 23947 |
rs29255803 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140746865 | ACTTACTGCTTATTC[A/C]TAGGTGACTTAAAAA | 23947 |
rs29256164 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Mid2 | Mm_Celera | X:140697825 | TGCCTCCCCATTCTA[C/G]TTTTTCTTTCGCTTC | 23947 |
rs29256165 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140697715 | CTCTGGCAAGAACAG[A/G]ATGAGGTTTTATTCC | 23947 |
rs29256166 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140697102 | TATAATAGTGTTGAA[C/T]ATGATGTGTATTTTA | 23947 |
rs29256167 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Mid2 | GRCm38.p3 | X:140697081 | CAACAAAGAACAGTG[A/G]GGCAGTATAATAGTG | 23947 |
rs29256168 | snp | A/C | 0.487535 | 0.077957 | intron-variant | Mid2 | GRCm38.p3 | X:140697055 | GATAATGAGATAAAT[A/C]CACTGAGAAGCAACA | 23947 |
rs29256169 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Mid2 | GRCm38.p3 | X:140696912 | TCTGATCTGGTTACA[C/G]AAAAGATCAGCTTTT | 23947 |
rs29256170 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Mid2 | GRCm38.p3 | X:140696547 | TTATTATTTGCTCTG[C/T]TCTTTTGATATGGTA | 23947 |
rs29256171 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140696009 | CCATCTGTTCGCAAG[C/T]CATGCTAGAAACCAG | 23947 |
rs29256172 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Mid2 | Mm_Celera | X:140695351 | CAAGAAGGATCATTG[A/G]AGTGTTAGTGGAAAA | 23947 |
rs29256173 | snp | G/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140695309 | AAAATAGGATGGTGT[G/T]GGTGTAGGGAGAAGC | 23947 |
rs29256284 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140746796 | AACAGTTGACAGCTT[C/T]GAGAAGATAGTCCCT | 23947 |
rs29256285 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mid2 | Mm_Celera | X:140746782 | TTGTGAGATTCCTTA[A/G]CAGTTGACAGCTTCG | 23947 |
rs29256286 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140746393 | TCAGATGGAGTCAGT[C/T]TGAAGCAGAGTTGGA | 23947 |
rs29256287 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140746280 | ACAGTGGGATTCTGG[A/C]AGGAGACAAGGCACT | 23947 |
rs29256288 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140746244 | TTTCACTTTTGATTA[C/T]ACTCTTGTGCCCTGT | 23947 |
rs29256289 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140745505 | AGTCTCCAGTGCTAG[A/G]GAATTAGCTTACATA | 23947 |
rs29256290 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140744714 | TTTAATTCTCAAAAA[A/C]ATCTAAGCAAATGAA | 23947 |
rs29256291 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140744595 | ACACTTATACAAATA[C/T]ACATACAGACTTCAC | 23947 |
rs29256292 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140744473 | AATCTGAAATTCATC[A/G]CCATCCTTATTCATT | 23947 |
rs29256293 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140744445 | GAAACACTTTTTCTC[C/T]GCTCTCTCACAGAAT | 23947 |
rs29256614 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140695209 | ACATACTTAAATGAT[A/G]AACATCTCTAGCTGT | 23947 |
rs29256615 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140695124 | GGCAATGAGTCATTA[C/T]GAATAACTAAATCCA | 23947 |
rs29256616 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140693801 | AGTTCAGTGCTTCTT[C/T]GCAGGAAAGAGTAAT | 23947 |
rs29256617 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140693667 | GTCTACTTAGCCTTT[C/T]TTATTATCAACAAAT | 23947 |
rs29256618 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140693632 | CCTTACTCATCATCT[G/T]GTCACTTATTTTCAA | 23947 |
rs29256619 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140693551 | CCATTCTTCCCTCTC[A/G]TCACTCTTTCCCCAC | 23947 |
rs29256620 | snp | C/T | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140692384 | AGTTACAAAATTTGG[C/T]ATTGGTGAATATCAC | 23947 |
rs29256621 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Mid2 | GRCm38.p3 | X:140692296 | ACCAGGAAATGATGG[C/T]AAATAGATATTTTCA | 23947 |
rs29256622 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Mid2 | Mm_Celera | X:140692042 | TGAGGTAGTGGAAAG[G/T]AAAGTAAAATATACT | 23947 |
rs29256623 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140691970 | AGGGAAAGAATAGGA[C/T]CAGAGCGAGGGTCAG | 23947 |
rs29256754 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140744354 | GATGATTCCAAATCT[C/G]TATGTAAATCTTTTC | 23947 |
rs29256755 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140744285 | AGCTTTCCTTACAAA[C/T]CCATTAGTGTTTAAG | 23947 |
rs29256756 | snp | G/T | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140743919 | ACGTTATTGAATGTG[G/T]TTTTTCAAGGCCACC | 23947 |
rs29256757 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140743094 | CTCTGATAGCTGAAG[G/T]GAGAGGCCCAAGTAT | 23947 |
rs29256758 | snp | A/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140743063 | TGATACGTCTTTGCA[A/G]GTCCTTATTTCAGTC | 23947 |
rs29256759 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Mid2 | Mm_Celera | X:140742955 | AGGAAATATACATAG[A/G]TTAAGGTATCAGAAC | 23947 |
rs29256760 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140742607 | AACAAACAAAAAAAG[A/C]ATTTAGGAGACAAGT | 23947 |
rs29256761 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Mid2 | Mm_Celera | X:140742418 | ATGCCTCCTTTAAAA[A/G]GAATTTAGGAAGCTG | 23947 |
rs29256762 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140741842 | AGCATATCTGTCTGT[C/T]TGTCTGTCTACCAGG | 23947 |
rs29256763 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140741795 | GCTTGCTGTCTACTG[C/T]TAGAAAACATCATAT | 23947 |
rs29257064 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140691679 | GGTTCTTAAAATTCC[C/G]TTTGAGAACAAGTGA | 23947 |
rs29257065 | snp | C/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140690713 | CACTGCACCTTAACA[C/G]AGTAGATGAGCAATG | 23947 |
rs29257066 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Mid2 | Mm_Celera | X:140690037 | GTATTGCAGAATCCA[C/T]ACAACCAGTGTTCCT | 23947 |
rs29257067 | snp | C/T | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140689504 | TTGAATGGAAACACA[C/T]TGTAGTGGGAAACAC | 23947 |
rs29257068 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140689256 | TGTGATGGTAACCCA[A/C]GGCCTGTAGTCTAAC | 23947 |
rs29257069 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Mid2 | Mm_Celera | X:140688993 | TCCTTACAAATGACT[A/G]GAAGTAAGTAAACGT | 23947 |
rs29257070 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140688822 | CACATCATTCAAACC[A/G]AGAGTGTCCCCGAAA | 23947 |
rs29257071 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140688791 | ATAGACAAGATAATC[C/T]CGTGGCCAAAGCAAT | 23947 |
rs29257072 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Mid2 | Mm_Celera | X:140688724 | GAGAAGATTTTTGTG[C/T]GCATGCACACACAAA | 23947 |
rs29257073 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140688608 | GCTCGGACGGAGGGA[A/G]CCTAGCCCAGTCCTT | 23947 |
rs29257244 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140741205 | AACTTTTAGCACTTG[C/T]ATTTTTATTTCCAAG | 23947 |
rs29257245 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140740264 | GAACATGTGTTTTCC[C/T]ACTCATAATTGTATG | 23947 |
rs29257246 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140740213 | CTTTCTATTTTTGGG[A/T]TTAATGGTTTGTATA | 23947 |
rs29257247 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140739819 | GGATGAATCACAGTA[C/T]TTAGTGCAAAGTACT | 23947 |
rs29257248 | snp | C/T | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140739746 | CCAACCATCTCTACT[C/T]TTTTTCATGCCTATA | 23947 |
rs29257249 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140738993 | CCATTGAGTTCATTT[A/G]TTGTTGTCTGTATGT | 23947 |
rs29257250 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140738774 | ACAAACTCCGGGCTA[A/C]ACTGATAGGATGTGC | 23947 |
rs29257251 | snp | C/T | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140738617 | GCCTTAGTGACAAAT[C/T]ACCCTGCAGATTTCT | 23947 |
rs29257252 | snp | A/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140738073 | TTGCTTTTACAATCA[A/G]AACAATGTTATTGAA | 23947 |
rs29257253 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140737992 | TAAAATGTAAACAAT[A/G]ATGATCTCCAGGTGG | 23947 |
rs29257484 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140688596 | TGTACTGACTGGGCT[A/C]GGACGGAGGGAACCT | 23947 |
rs29257485 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140688554 | TTTGGCTCTCTTGCT[A/G]TGATGGTTCAACTGT | 23947 |
rs29257486 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140688514 | TCCTCCCAGCAGATA[G/T]CTCCATTCCAATCTC | 23947 |
rs29257487 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140688185 | AAGGCCAAGGCTATA[C/T]AACACAAATGAAATG | 23947 |
rs29257488 | snp | A/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140688172 | TGGAGAGCTCAAAAA[A/G]GCCAAGGCTATACAA | 23947 |
rs29257489 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140688038 | GAAGTGAGATTTTTT[A/T]AAAAGCAATTATTTA | 23947 |
rs29257490 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140687979 | CTAAGTTTCTTGAGA[G/T]ACTAAATAAAAAAGA | 23947 |
rs29257491 | snp | A/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140687870 | AATGGATCGTGGCAA[A/G]TATAGAGTCCGGACA | 23947 |
rs29257492 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140687861 | CCTCCCTGGAATGGA[G/T]CGTGGCAAGTATAGA | 23947 |
rs29257537 | snp | A/G | 0.489796 | 0.070696 | downstream-variant-500B | Mid2 | Mm_Celera | X:140768181 | AGGGTCATGTAACAT[A/G]GAGTGAATCAGTCAA | 23947 |
rs29257538 | snp | G/T | 0.197531 | 0.244432 | downstream-variant-500B | Mid2 | Mm_Celera | X:140768152 | TTCAGAGTTGCCATT[G/T]CACTGAGACTAAAAG | 23947 |
rs29257539 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Mid2 | Mm_Celera | X:140767551 | ACTATTTTTTATCAA[A/G]TGCTTTACCCCAGGC | 23947 |
rs29257540 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Mid2 | Mm_Celera | X:140767205 | AGCTCAGACATTCTA[A/G]GTGAATTCTCAGTTT | 23947 |
rs29257541 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Mid2 | Mm_Celera | X:140767183 | AAATCACTTATATAT[A/G]CTTTTCAGCTCAGAC | 23947 |
rs29257542 | snp | A/G | 0.21875 | 0.248039 | utr-variant-3-prime | Mid2 | Mm_Celera | X:140766526 | TTGTCTTTGGAGCAC[A/G]TGGTATCATTCTACC | 23947 |
rs29257543 | snp | A/G/T | 0.21875 | 0.248039 | utr-variant-3-prime | Mid2 | Mm_Celera | X:140766420 | GGGGGCAAGTTGGTT[A/G/T]CTTTAGTCTGTATTG | 23947 |
rs29257684 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140737802 | TTATAGGGCTCACTT[A/G]ATGATCAGTACTTTG | 23947 |
rs29257685 | snp | A/C | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140737783 | CCATGGTAAATGTGT[A/C]AAGTTATAGGGCTCA | 23947 |
rs29257686 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Mid2 | Mm_Celera | X:140737330 | AAAGCATAATAACTG[A/C]TAGAGAGAAAATGAT | 23947 |
rs29257687 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140737261 | GACCTACAGCGATTT[C/T]TGGTATGAGTTATGG | 23947 |
rs29257688 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140737249 | GGAAAGCTTGGAGAC[A/C]TACAGCGATTTCTGG | 23947 |
rs29257689 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140737174 | TGATTCTGTAAAAGG[A/G]TGCATTCTGATATAG | 23947 |
rs29257690 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140736752 | AACATTCTATACCTC[A/G]ACCTGGATGCTGGTT | 23947 |
rs29257691 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140735740 | ACCAACCAATATTAC[C/T]AGTTGAGGAAAGGAG | 23947 |
rs29257692 | snp | A/C | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140735281 | AACCATTGTCTATTT[A/C]TCGGCTTTCTAGAGT | 23947 |
rs29257693 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140734263 | TAGTTACCAATGAGG[A/G]AAAGGTAAAGAAGAG | 23947 |
rs29257974 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | Mid2 | Mm_Celera | X:140766358 | AGAAATGAATAATTC[G/T]AATTGCTGTTTGACT | 23947 |
rs29257975 | snp | A/C | 0.48 | 0.0979796 | utr-variant-3-prime | Mid2 | Mm_Celera | X:140765939 | TCTTCTCAGCTAACT[A/C]GTGACCTCTGGAATT | 23947 |
rs29257976 | snp | A/G | 0.165289 | 0.235211 | utr-variant-3-prime | Mid2 | Mm_Celera | X:140765904 | ATGGACTGCAGCTTA[A/G]ACTACCTTTCCTCAT | 23947 |
rs29257977 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime | Mid2 | Mm_Celera | X:140764676 | AGAGAAGTGTCTCGT[A/G]TAGCCTAATTTCATT | 23947 |
rs29257978 | snp | C/T | 0.18 | 0.24 | utr-variant-3-prime | Mid2 | Mm_Celera | X:140764215 | CTAGTAATGGCTAGT[C/T]TGACCAGGTAGAATT | 23947 |
rs29257979 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Mid2 | Mm_Celera | X:140764037 | TTGTGCATTAAAAAT[C/T]ATGTTTGAATTCATG | 23947 |
rs29257980 | snp | A/G | 0.21875 | 0.248039 | utr-variant-3-prime | Mid2 | Mm_Celera | X:140763992 | CCATTGGAAGCACTC[A/G]AAATAACTAGATATC | 23947 |
rs29257981 | snp | C/T | 0.408163 | 0.193609 | synonymous-codon | Mid2 | Mm_Celera | X:140763644 | GCGTCTAGGTGTCCT[C/T]CTGGATTATGACAAC | 23947 |
rs29257982 | snp | C/G | 0.277778 | 0.248452 | synonymous-codon | Mid2 | Mm_Celera | X:140763641 | GAAGCGTCTAGGTGT[C/G]CTTCTGGATTATGAC | 23947 |
rs29257983 | snp | C/T | 0.18 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140763462 | AATAAAAGTTTCTGT[C/T]GTCTCCACTGTCTTA | 23947 |
rs31038056 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mid2 | Mm_Celera | X:140727173 | TTAACACGCGCGCGC[A/G]CGCGCGCGCGCACAC | 23947 |
rs31043577 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Mid2 | Mm_Celera | X:140712076 | AAATGATTTTTCAAC[G/T]GTGTGTCATAAGTTT | 23947 |
rs31068444 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mid2 | GRCm38.p3 | X:140713272 | TATACTTTGCCAAGC[C/T]TAGCTTTTATGTGGG | 23947 |
rs31069945 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mid2 | Mm_Celera | X:140673638 | TTTTGATTTTCATAT[A/G]TCAGACAATGTGGTT | 23947 |
rs31083298 | snp | A/C | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140757341 | AAAAACAAAAAAAAA[A/C]CCAAAAACAAAAACA | 23947 |
rs31096217 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Mid2 | GRCm38.p3 | X:140734584 | ACTAGTCTTGTCTCT[C/G]TCACTCCTAACTGTG | 23947 |
rs31101349 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Mid2 | GRCm38.p3 | X:140718149 | TCCCTCCTGCCATTG[A/C]CCCTTTGCTCTGAAT | 23947 |
rs31108451 | snp | A/G | 0.5 | 0 | intron-variant | Mid2 | GRCm38.p3 | X:140672232 | GGAAGAGGATTGAGC[A/G]TAACCCAGGTTACTC | 23947 |
rs31114293 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Mid2 | GRCm38.p3 | X:140719635 | TAAATTTTCCCTGCA[G/T]CCCAGTCCAAGAATA | 23947 |
rs31117294 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mid2 | GRCm38.p3 | X:140705845 | CCTGGTCACAAAGGA[C/T]TGTAATCATGTTAAG | 23947 |
rs31121906 | snp | A/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140675268 | CCTACTTTGACCTTA[A/T]ATAAGGCCATTGTGA | 23947 |
rs31123127 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Mid2 | Mm_Celera | X:140733069 | CTCTCTCTCTCTCAC[A/T]CACACACACACACAC | 23947 |
rs31126204 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Mid2 | Mm_Celera | X:140705642 | AGTAGCTAACACTTA[C/T]TAATATTTAATATGC | 23947 |
rs31127243 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mid2 | GRCm38.p3 | X:140714844 | CCCTTTTGTTAGTCA[C/T]ATTCCAAAGAGCTTA | 23947 |
rs31147262 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Mid2 | GRCm38.p3 | X:140704884 | GAGTCGATTGGCTTT[C/G]TAATGGAATGGAATT | 23947 |
rs31158669 | snp | C/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140715293 | TTAAAAATATGTACA[C/T]AATGTCTAAGTAATA | 23947 |
rs31167977 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Mid2 | GRCm38.p3 | X:140733067 | CTCTCTCTCTCTCTC[A/T]CACACACACACACAC | 23947 |
rs31168836 | snp | A/G | 0.5 | 0 | intron-variant | Mid2 | GRCm38.p3 | X:140715630 | TTCCTGGAATAAGAT[A/G]GCTAAGAGACCTTGT | 23947 |
rs31174489 | snp | C/T | 0.432133 | 0.171253 | upstream-variant-2KB, intron-variant | Mid2 | GRCm38.p3 | X:140677648 | GAATTTGGGAGGAAA[C/T]GATCCATGCTGAGTG | 23947 |
rs31174934 | snp | A/T | 0.5 | 0 | intron-variant | Mid2 | GRCm38.p3 | X:140667742 | ATCCCTCCTCTAAAA[A/T]CAGGGCAACTTGCTC | 23947 |
rs31177139 | snp | A/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140708639 | AGCAACCCCTCTTAT[A/T]GTTGACCAGGCCTAC | 23947 |
rs31200544 | snp | A/C | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140715896 | TTTATTTACATTTCA[A/C]TGTTATCCCCTTCCA | 23947 |
rs31200812 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140677309 | TAGGATAAAACAGAT[C/T]TCCATGTGTGCTAAT | 23947 |
rs31203123 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mid2 | Mm_Celera | X:140715086 | TTCTTTCCTAGACTG[C/T]CCATTTGGAATCTAG | 23947 |
rs31225822 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mid2 | GRCm38.p3 | X:140690337 | GACTAATGGTGTATA[C/T]AACCGTACTCAACAA | 23947 |
rs31259359 | snp | C/T | 0.5 | 0 | intron-variant | Mid2 | GRCm38.p3 | X:140715994 | CCCACCCATCCACTC[C/T]CATTCTCCCGCCCTG | 23947 |
rs31264223 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mid2 | GRCm38.p3 | X:140705847 | TGGTCACAAAGGATT[A/G]TAATCATGTTAAGAA | 23947 |
rs31272168 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mid2 | Mm_Celera | X:140727174 | TAACACGCGCGCGCA[C/T]GCGCGCGCGCACACA | 23947 |
rs31286248 | snp | C/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140705683 | GTGTTAAGTATTTTA[C/T]ATGTATTATTTCATT | 23947 |
rs31298834 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Mid2 | GRCm38.p3 | X:140663504 | GGTTTTAAAACATTT[C/T]CTCCCATTCCCAATG | 23947 |
rs31302824 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Mid2 | GRCm38.p3 | X:140718010 | TCTTTTGGCCCTCAA[A/C]GCCTGGGGATTGTGT | 23947 |
rs31303462 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Mid2 | GRCm38.p3 | X:140672784 | TCTTTTTGTTGTGTC[C/T]CTTCCTCTGCTAAAA | 23947 |
rs31304937 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mid2 | Mm_Celera | X:140715090 | TTCCTAGACTGCCCA[C/T]TTGGAATCTAGTTCT | 23947 |
rs31307104 | snp | C/T | 0.5 | 0 | intron-variant | Mid2 | GRCm38.p3 | X:140704863 | TGCTCCAAACCAATT[C/T]AGGAGGAGTCGATTG | 23947 |
rs31309088 | snp | A/G | 0.5 | 0 | intron-variant | Mid2 | GRCm38.p3 | X:140715469 | CCAAAGACCTACCAA[A/G]AGATTATGGAAGGCT | 23947 |
rs31309773 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Mid2 | GRCm38.p3 | X:140713275 | ACTTTGCCAAGCTTA[G/T]CTTTTATGTGGGTGC | 23947 |
rs31310005 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Mid2 | GRCm38.p3 | X:140662467 | ACCTGTCATGGTTTG[A/G]GTTTGAAATGTCCCA | 23947 |
rs31311843 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mid2 | GRCm38.p3 | X:140715030 | TAAGCCACATTGGCT[A/G]TCTAAATCTGATCCA | 23947 |
rs31316392 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mid2 | GRCm38.p3 | X:140705915 | GATATTTAGCATGAA[A/G]GTATTTTAAGAGTGG | 23947 |
rs31318463 | snp | A/T | 0.5 | 0 | intron-variant | Mid2 | GRCm38.p3 | X:140740408 | GGTATCTGGGTACTG[A/T]GCCTCAGGGATCTAC | 23947 |
rs31323140 | snp | C/T | 0.5 | 0 | synonymous-codon | Mid2 | GRCm38.p3 | X:140678678 | CCGAGACCATCAGGT[C/T]GCTTCTCTGAATGAT | 23947 |
rs31323769 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mid2 | Mm_Celera | X:140674627 | CTTTTATTTTTTCTA[C/T]GTTTGACTATTTGCT | 23947 |
rs31335751 | snp | C/T | 0.5 | 0 | intron-variant | Mid2 | GRCm38.p3 | X:140684612 | GGGTGGGGGTCACTG[C/T]GAGTTTGAAGCCTGC | 23947 |
rs31348296 | snp | C/T | 0.497041 | 0.0383476 | upstream-variant-2KB | Mid2 | GRCm38.p3 | X:140663630 | AACTTTTACATCTCT[C/T]GGTGCTGTACTTCCT | 23947 |
rs31351428 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mid2 | GRCm38.p3 | X:140715954 | CATCCCCTCTCCTCT[A/G]TGCCTCTATGAGGGT | 23947 |
rs31353310 | snp | G/T | 0.415225 | 0.187619 | intron-variant | Mid2 | GRCm38.p3 | X:140681125 | TGACTAATCAGTAAT[G/T]TTTGGAGAAAGAGTG | 23947 |
rs31359009 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Mid2 | Mm_Celera | X:140705821 | TGAGACTACAGAGGC[A/T]TGGAGAGACCTGGTC | 23947 |
rs31372212 | snp | A/G | 0.5 | 0 | intron-variant | Mid2 | GRCm38.p3 | X:140704969 | ATTACAGATGAGTAG[A/G]CAAACTGCACAGTGT | 23947 |
rs31394762 | snp | C/T | 0.5 | 0 | intron-variant | Mid2 | GRCm38.p3 | X:140704486 | ATAGAACCACACGTT[C/T]CCACCCTTTGCTCTT | 23947 |
rs31398236 | snp | C/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140721833 | CTGGGTTACCTCACT[C/T]GGGATGATTTTTTTT | 23947 |
rs33847734 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Mid2 | GRCm38.p3 | X:140687733 | AAACAGGCTTTGATG[G/T]CAATACTTGATGTCT | 23947 |
rs33847735 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140687656 | ATATCAAAGCCCCAG[A/T]GTTGTGATCTTGCCT | 23947 |
rs33847736 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140687522 | CTGTCTCTTGCTTTT[C/T]GCGACTAAATGACAT | 23947 |
rs33847737 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140686510 | AGCATTCCTGGTCAC[A/G]ATAGAAGTGGAGGTT | 23947 |
rs33847738 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140685926 | CATGGTTACAAAACA[A/G]TGTAAGCACAAGAAG | 23947 |
rs33847739 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140685728 | TGTCTTCAAAAGAAA[A/G]GCACTGAAGACAGAA | 23947 |
rs33847740 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140685006 | GCTGTTTTGTCACTG[A/G]TCTTTTAGTCACTAG | 23947 |
rs33847741 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140684294 | TTGCTTATAAAGCTG[A/G]CATCTCTGTTGTCTC | 23947 |
rs33847742 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140684171 | GTTGGGATTTATGTT[C/T]GTTGAGGTATGGATT | 23947 |
rs33847743 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Mid2 | Mm_Celera | X:140684140 | TCTGTCAAACTTAAA[A/T]AAAAATGAAAAAAAA | 23947 |
rs33847794 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140684128 | TTTAATAAAATTTCT[A/G]TCAAACTTAAATAAA | 23947 |
rs33847795 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Mid2 | Mm_Celera | X:140683981 | GACCTCTATGCTAAA[A/T]TAGAAAAATCTTTAG | 23947 |
rs33847796 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Mid2 | Mm_Celera | X:140683819 | ATATGAAGATGAACA[G/T]CTGTGATATCTACTG | 23947 |
rs33847797 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140683707 | GCATAAATATGTAGG[C/T]ACTGTCATCTGCGAG | 23947 |
rs33847798 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mid2 | GRCm38.p3 | X:140683512 | CTCATTCTGTCACTG[A/C]TTTTCCCCAGTCAAT | 23947 |
rs33847799 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Mid2 | GRCm38.p3 | X:140683205 | GCTATATTTACATAT[C/G]AAGACTCTTGTTATT | 23947 |
rs33847800 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140682333 | CAGCTTCATCTACTC[G/T]GGTGAACTTCCTAAC | 23947 |
rs33847801 | snp | G/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140682315 | CACGACTCTCAATTT[G/T]GCCAGCTTCATCTAC | 23947 |
rs33847802 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140681001 | GCTATTCCAGAATAG[C/T]GAAAAACATGGGGTG | 23947 |
rs33847803 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Mid2 | Mm_Celera | X:140680146 | GGAAGGTCCCAGTAG[C/T]ATGGAGGAAGGCGGG | 23947 |
rs33847844 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Mid2 | Mm_Celera | X:140680142 | AGAAGGAAGGTCCCA[A/G]TAGCATGGAGGAAGG | 23947 |
rs33847845 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140679578 | TTACCTTACTTTGAC[A/G]GTCACAAATGTCAGA | 23947 |
rs33847846 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Mid2 | Mm_Celera | X:140679556 | GTGCCTGGTTTTGAA[A/G]GGCCTTTTACCTTAC | 23947 |
rs33847847 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mid2 | Mm_Celera | X:140679469 | GGTTCTATCTTACAA[A/G]TCTCCAGGCCTTTGT | 23947 |
rs33847848 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Mid2 | GRCm38.p3 | X:140679452 | TAACACACTGGTTTG[C/T]AGGTTCTATCTTACA | 23947 |
rs33847849 | snp | C/G | 0.5 | 0 | intron-variant | Mid2 | GRCm38.p3 | X:140679309 | AAAATTGCCAGTGAG[C/G]ACTTCACTTAGAGCT | 23947 |
rs33847850 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140679145 | GGAGGACATTAGTAT[A/G]TGCGTGTGTTTGCAA | 23947 |
rs33847851 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140679076 | ATTTGGCTGGGTCTC[C/T]GTGGAGGTGTGGGTG | 23947 |
rs33847852 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Mid2 | Mm_Celera | X:140678891 | ATAAGGCTGCTTGTA[C/G]TTCTGGGGAAGTAAG | 23947 |
rs33847853 | snp | A/G | 0.297521 | 0.245442 | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140677930 | TCCCTTGGTTACAAT[A/G]TAATTATTCTGCAAT | 23947 |
rs33847874 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140677682 | GAGCTGGAATGGTAA[G/T]GGTAATCAGGAAACC | 23947 |
rs33847875 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140676873 | AACGACTGTGGGAAA[A/G]TGGAGAGAATGACAG | 23947 |
rs33847876 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140676655 | AAATACCAGTGGAAG[A/G]ATCAAATTTTCAGGT | 23947 |
rs33847877 | snp | A/G | 0.260355 | 0.249785 | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140676581 | ATAATTGTACTCAAT[A/G]TTGGTGATTCCCATG | 23947 |
rs33847878 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140676243 | TTATCTAAGGAAATA[A/G]TCCTACCCTGTGTGG | 23947 |
rs33847879 | snp | C/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140676178 | TTGCAAGGATGGTCA[C/G]AGAGTGTCAGTTCAT | 23947 |
rs33847880 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Mid2 | Mm_Celera | X:140675924 | CTATGTGCCTTCTTA[G/T]GTTTGCTCTGAGCAA | 23947 |
rs33847881 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140675539 | GTTGTAATAGAAGTA[C/T]AGTGTCAGATGGAGA | 23947 |
rs33847882 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140675447 | ACGGAACATGTAAAC[G/T]CGACTTTCTGCAATG | 23947 |
rs33847883 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140674812 | GGCTAGAACAGCACT[A/G]ATGAGAATCAGGGGC | 23947 |
rs33847914 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140672879 | AAGAACTGAGGCTTA[A/G]GAATTTTCTGACACT | 23947 |
rs33847915 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140672014 | GAATTCTGTCAAGTG[C/T]AGATCACAGCTGCTT | 23947 |
rs33847916 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Mid2 | Mm_Celera | X:140671806 | CCAGCTCTTTTCTCA[A/G]TCTATAGAACAAAGG | 23947 |
rs33847917 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Mid2 | GRCm38.p3 | X:140671441 | CAGTGCTTACCACTT[C/T]TTAGCCTTCCTAGTT | 23947 |
rs33867144 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mid2 | GRCm38.p3 | X:140718266 | GGGAAGTGTGATAGC[A/G]TGGCACCAGGAGGAT | 23947 |
rs33870022 | snp | G/T | 0.5 | 0 | intron-variant | Mid2 | GRCm38.p3 | X:140667519 | GATGCAGTCAGGGTG[G/T]GTGATGTGTGGAGTA | 23947 |
rs33870048 | snp | A/G | 0.5 | 0 | intron-variant | Mid2 | GRCm38.p3 | X:140715785 | GAGCAGCACTCCCCT[A/G]TGTGTGCCTACAGAC | 23947 |
rs33870442 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mid2 | GRCm38.p3 | X:140718182 | TGATACTAAATAGGT[A/G]ATGATGTGGTTCCTG | 23947 |
rs33874235 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Mid2 | Mm_Celera | X:140715046 | TCTAAATCTGATCCA[A/T]GGGAAACTGATAGTC | 23947 |
rs33875595 | snp | A/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140718768 | TTATGCTCATTTTTT[A/T]AAAAATCCATTTTCA | 23947 |
rs33876486 | snp | A/C | 0.375 | 0.216506 | intron-variant | Mid2 | Mm_Celera | X:140675863 | ATTTAATGTACATAA[A/C]GTGCTTAACATAGCA | 23947 |
rs33879522 | snp | A/G | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140715241 | GACTTTCTGGGTTTA[A/G]CTTAATAAATGGGAG | 23947 |
rs33879681 | snp | G/T | 0.5 | 0 | intron-variant | Mid2 | GRCm38.p3 | X:140682789 | AGAATTATGTTATAG[G/T]AAGTATATTAGTGCA | 23947 |
rs45700236 | snp | C/G | | | intron-variant | Mid2 | GRCm38.p3 | X:140665531 | CCTGCCGCTGCCCTC[C/G]TGGGAAGGAGTTTGC | 23947 |
rs45726936 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140740695 | ACAGAGCCATATTAA[C/T]TAAAATAACTAACAT | 23947 |
rs45895872 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140740746 | GAAACATAAATTAAT[G/T]AAATTAGAATAAAAA | 23947 |
rs45896292 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140714050 | TCAATGGCACTGAAA[C/T]TTACAATGCTCTGCA | 23947 |
rs46363005 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140713261 | GCTACTAGAGCTATA[C/T]TTTGCCAAGCCTATC | 23947 |
rs46482784 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140706792 | CATGGGCATCTACAT[A/G]CACATGCATGCACAC | 23947 |
rs46676228 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140711283 | TTAAAATGCAGCTGG[A/G]GAAAGCTTTTGATTT | 23947 |
rs46832259 | snp | A/G | | | utr-variant-3-prime | Mid2 | Mm_Celera | X:140766874 | TGACCATTTAACATC[A/G]TCAAGAAAGATGATT | 23947 |
rs46894511 | snp | A/G | | | intron-variant | Mid2 | GRCm38.p3 | X:140680263 | TCAGAATAGATTCAC[A/G]ATCTTGTCTGTAATT | 23947 |
rs46997159 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140718687 | TATTTCTATTATCCT[A/G]TATAGAGTAGAGGAA | 23947 |
rs47003082 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140706759 | GCTCCAAAGCATCCA[A/G]TGCCCTCTTCTGGCT | 23947 |
rs47127922 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140710852 | TCCAGTCCAGCCACA[C/T]CTACACAGGGAAAGC | 23947 |
rs47243812 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140706847 | CTTTTAAAGATTGGA[C/T]TTTGCAAATGGTTGC | 23947 |
rs47328271 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140711257 | AATGTGTTGCTTTTC[C/T]ATTTTCACTTTTAAA | 23947 |
rs47351389 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140740633 | TCCATGAGATCCCAT[G/T]TATCCACTGTTCACA | 23947 |
rs47557597 | snp | C/G | | | intron-variant | Mid2 | GRCm38.p3 | X:140665635 | AGCGGCTCAGCTCTC[C/G]TGGCGCCTAGGCGCA | 23947 |
rs47771655 | snp | A/G | | | intron-variant | Mid2 | GRCm38.p3 | X:140716457 | TTGGTTTTCACAACT[A/G]CTTCTGAGATAGTGT | 23947 |
rs47845622 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140673622 | ATAAGGATAAACCAT[A/G]TTTTGATTTTCATAT | 23947 |
rs47848272 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140740403 | GTTAGGGTATCTGGG[C/T]ACTGTGCCTCAGGGA | 23947 |
rs48034966 | snp | A/G | | | intron-variant | Mid2 | GRCm38.p3 | X:140716506 | CAGAAAGATAAGCTC[A/G]GAGAAAAGTGATTAG | 23947 |
rs48235029 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140716132 | ATCCCTCCATGTGTA[C/T]TCCTTGGTTGGTGGT | 23947 |
rs48260310 | snp | G/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140718281 | GTGGCACCAGGAGGA[G/T]AGTCTGTCTTCCTTT | 23947 |
rs49044619 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140740616 | TACAAGTTCCTTTTA[A/G]TTCCATGAGATCCCA | 23947 |
rs49208067 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140707707 | CAACTGAGGAATGGC[C/T]GAGAAGCACCTAAAG | 23947 |
rs49245772 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140669683 | TTTAAAAATCACCAG[A/G]TATTTAAAAATGCAT | 23947 |
rs49248564 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140740444 | TGCCTTTCCAGCACT[C/T]GAATATTAAGTGTGT | 23947 |
rs49289174 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140740754 | AATTAATGAAATTAG[A/G]ATAAAAAATTCAGGT | 23947 |
rs49307932 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140706014 | GAATTCTGCAGGAGA[A/G]CTAGGGATATAGCTC | 23947 |
rs49384858 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140668748 | TGTTAGTGCCCTTTC[C/T]CACTTCTCACCTTCA | 23947 |
rs49403478 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140740560 | AAGGGTTTTATCCTA[G/T]TCTGTCTATCTCTTC | 23947 |
rs49597949 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140740669 | TCCTGAATGACTGGT[A/C]AAGTTGTACTACAGA | 23947 |
rs49630055 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140674402 | GCCCCACCTCTCAAG[A/T]GTTGGGATTGCAGGC | 23947 |
rs49696511 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140714893 | ATTTTTATTAACGTC[C/T]TATATGACCATCCCA | 23947 |
rs50228440 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140705961 | GTGGGGGGGGGGCAG[A/G]AGTGGAGGTAAATTT | 23947 |
rs50436605 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140740484 | CCTAGATGGCTTTTT[A/T]TAAAATTTGGGCTCT | 23947 |
rs50565164 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140710506 | TCTTAAAACATTAAT[A/G]CACCTGATATTATTT | 23947 |
rs50776585 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140691595 | CCTCTTCCAGCAGTG[C/T]TAAACTGTTTAAATG | 23947 |
rs50846713 | snp | A/G | | | intron-variant | Mid2 | GRCm38.p3 | X:140716611 | AAAAGTACTAATAAA[A/G]CACAGAAACAGCACA | 23947 |
rs50900038 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140740485 | CTAGATGGCTTTTTT[A/T]AAAATTTGGGCTCTG | 23947 |
rs50971286 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140707407 | AAATGCCAGTGGATT[C/T]TTCTACATGCTAACC | 23947 |
rs51087604 | snp | A/G | | | intron-variant | Mid2 | GRCm38.p3 | X:140713307 | AAGGCTTCAAGCTCT[A/G]GTCCCCTTACTTATG | 23947 |
rs51090218 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140714278 | TTTGGGCAAGTCTGA[C/T]CAAAATTTTGGGATG | 23947 |
rs51188336 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140710362 | TGTGCCACCGCACCC[A/G]GTTTAGGTGGTGGTA | 23947 |
rs51212566 | snp | A/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140716511 | AGATAAGCTCAGAGA[A/T]AAGTGATTAGAATCC | 23947 |
rs51241695 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140714155 | CTTTCCTGCAGTGGA[C/T]TCCAGCATCTTGAGC | 23947 |
rs51292085 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140717105 | TATAGACATGAAATA[G/T]CTTACAGAGCTCTCT | 23947 |
rs51495324 | snp | G/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140707022 | GAGGCTAGGCATGGA[G/T]AGCCACTTAAGAGAC | 23947 |
rs51586728 | snp | G/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140707632 | GAGTTCAAGAAGTTA[G/T]ACTCCAGAGAATCAA | 23947 |
rs51668565 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140710833 | TGACTTCAATACTAC[A/G]TAATCCAGTCCAGCC | 23947 |
rs51756416 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140714124 | AGGGCAAGGTAAGTG[C/T]TACCACCATGGTTCT | 23947 |
rs52092235 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140707270 | GCATTTAAAATGTGC[C/G]GGAGAGACTTGGAAT | 23947 |
rs52113964 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140707214 | AGCAAACTGAAACAA[A/G]ATAAAAATTCCAATC | 23947 |
rs52198164 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140707228 | AGATAAAAATTCCAA[C/T]CCTGAAACCACTAAA | 23947 |
rs52230921 | snp | C/G | | | intron-variant | Mid2 | GRCm38.p3 | X:140681698 | AAAGAACTATTGtct[C/G]tctctctctctctct | 23947 |
rs52241607 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140708615 | GTAAGAGAGAAATAA[A/G]AGAGGGCAAGCAACC | 23947 |
rs52320291 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140708612 | AGAGTAAGAGAGAAA[G/T]AAAAGAGGGCAAGCA | 23947 |
rs52508635 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140707229 | GATAAAAATTCCAAT[A/C]CTGAAACCACTAAAA | 23947 |
rs52526159 | snp | A/G | | | intron-variant | Mid2 | GRCm38.p3 | X:140686915 | AGAAGAGGAGGAAGA[A/G]GAGGGGAAGAAGGAG | 23947 |
rs211747115 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140692998 | CATATTATATTGGTT[C/G]TCAAGTTCATTGTTC | 23947 |
rs211767777 | snp | C/T | | | downstream-variant-500B | Mid2 | Mm_Celera | X:140767913 | AGTATATAGTTAATA[C/T]ATCTAATGAAATGAA | 23947 |
rs211876376 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140734154 | AAGTGGAAAAGACTC[-/TG]TAATACAATTGCAGT | 23947 |
rs211891964 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140722390 | ACTTTTGGGCATCTA[C/G]CAAATGGATGCTCCC | 23947 |
rs211903032 | in-del | -/AAA | | | intron-variant | Mid2 | Mm_Celera | X:140674155 | TTTTGTTGTGATCTT[-/AAA]TAAAAAAACCCAAAA | 23947 |
rs211953026 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140705004 | TTGCCAGAGAATAGA[A/T]TTAAGCACCTTCACG | 23947 |
rs211954426 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140723330 | TGTGGATTCAGTTGT[A/G]AGCAAAACAATGGCC | 23947 |
rs211983963 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140668689 | GTTCAGATGACTGGT[A/G]GCAAGAAAAGACAAT | 23947 |
rs212000850 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140745646 | TTGCTGTGTAATCAT[A/G]AAGATTAGAGTTCAT | 23947 |
rs212060324 | in-del | -/G | | | intron-variant | Mid2 | Mm_Celera | X:140705192 | TGTTGATAATTTTAT[-/G]GTTTTTTTTAAAATA | 23947 |
rs212078844 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140712378 | TGCCTCCCTCCCTCC[C/T]TCCTTCTCTTCCTTC | 23947 |
rs212095312 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140733450 | TGATCTCAGATGCTA[C/T]ATAAAGTCTTACCAA | 23947 |
rs212109594 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140725269 | GGACAGTCCCCCGTT[C/T]CTTCCAGTTTGGGAC | 23947 |
rs212111379 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140714253 | AACCCAGGGCGATAT[A/G]GAACTCACTTTTGGG | 23947 |
rs212183669 | in-del | -/AT | | | intron-variant | Mid2 | GRCm38.p3 | X:140710243 | CCTTTTCCATCTGAG[-/AT]ATAGGGCCTTCATGT | 23947 |
rs212257089 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140747675 | ATACTACAAAAATAG[A/C]TGTTCAATGTGAAAC | 23947 |
rs212309687 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140724152 | ATGTGCTACCAATTT[A/G]TAGTATAGTCACATC | 23947 |
rs212340066 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140672231 | GGGAAGAGGATTGAG[C/T]GTAACCCAGGTTACT | 23947 |
rs212431920 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140756194 | CTCACCCGACTCTTT[A/C]CCCTAACTGAGCATC | 23947 |
rs212444362 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140756839 | GTTGATAGCTCACAT[C/T]ATGAACTATAAACAG | 23947 |
rs212462671 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140740262 | GTGAACATGTGTTTT[A/C]CTACTCATAATTGTA | 23947 |
rs212524590 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140674570 | CCTGGAACCTTTGTC[A/C]AAAACGAGTTGGTTA | 23947 |
rs212525304 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140751987 | ATGAATAGACTTTTT[A/T]AAATAAACCCTCCTC | 23947 |
rs212613781 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140685174 | CAAGAATTATTGAAG[A/T]TAGAGTAGTGACATT | 23947 |
rs212652424 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140758292 | GGTAAAAGGTTACTT[G/T]GAAAAACAGGGATGG | 23947 |
rs212665190 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140750498 | CCATGTAATGAGAAA[A/G]CAGTATTTTGCTTTG | 23947 |
rs212673069 | in-del | -/GCGCGCGC | | | intron-variant | Mid2 | GRCm38.p3 | X:140718901 | TGTTCTGGGTGATAT[-/GCGCGCGC]GCGCGCGCGTGTGTG | 23947 |
rs212673621 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140693878 | TAAATTAGAGACTGT[A/C]TTTATTTACATTTCA | 23947 |
rs212700692 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140696137 | TCCATCTACTCCTCC[C/T]CTGTTTCCATTTAGA | 23947 |
rs212724910 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140747045 | GTTAAAGGCTCAAGT[G/T]AAATACATAACATAT | 23947 |
rs212753153 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140684317 | GTTGTCTCTGAACTG[G/T]TCAAGACTTCTCCCC | 23947 |
rs212796450 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140757761 | ATATGATAAGGTCCT[A/G]TCTCAAATCTTTAAA | 23947 |
rs212840960 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140707670 | TATTAGAAATGGGGT[A/T]CAGAGCTAAACAAAG | 23947 |
rs212911460 | in-del | -/C | | | upstream-variant-2KB | Mid2 | Mm_Celera | X:140664066 | TAGGGACATTGTATT[-/C]CTGGATGGCTAGCAT | 23947 |
rs212970727 | in-del | -/AA | | | intron-variant | Mid2 | Mm_Celera | X:140673109 | CTGGAAAAAAAGTAG[-/AA]AAAAAAAAAAGAAGC | 23947 |
rs212978356 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140760794 | CCCTTCTGCTCTGAA[C/T]TTTCATGATACTGAG | 23947 |
rs213036064 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140711512 | TTTAGTATGATATTC[A/G]TTATTTGTTTTTAGC | 23947 |
rs213082233 | in-del | -/A | | | downstream-variant-500B | Mid2 | Mm_Celera | X:140768163 | CATTGCACTGAGACT[-/A]AAAGGGTCATGTAAC | 23947 |
rs213087019 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140709493 | TGTGAAGGCTTGATG[C/T]CCCAGTGTGAGGGAA | 23947 |
rs213091267 | in-del | -/A | | | intron-variant | Mid2 | Mm_Celera | X:140750222 | GTTGTTTTCAGGATT[-/A]AAAAAACAGTCACTT | 23947 |
rs213102986 | snp | C/G/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140708132 | AGGACCTAGCTATAC[C/G/T]ACTGCTGGGCATATA | 23947 |
rs213111521 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140716939 | AACATAGATAATCTG[C/T]TTCAGAGTTGGCAGC | 23947 |
rs213182521 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140718037 | GTGTTAATTATGGGG[C/T]ATCCTAGAGCAGAAA | 23947 |
rs213184088 | snp | A/G | | | intron-variant | Mid2 | GRCm38.p3 | X:140709021 | TTCTTAGAAGGGAGA[A/G]CAAAATACCCATGGG | 23947 |
rs213197573 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140726349 | ACTTCCCTACCCACT[C/T]CTTCCCATTTTTTTG | 23947 |
rs213352593 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140701401 | ATACTGGAGCCTCCC[A/G]TGGGGAGACATGGTG | 23947 |
rs213402986 | in-del | -/A | | | upstream-variant-2KB | Mid2 | Mm_Celera | X:140663150 | TAGATGCACACACAT[-/A]AAATATACATATATA | 23947 |
rs213408694 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140695986 | CTTCACCTAAGCATA[A/G]CACTCTTCCATCTGT | 23947 |
rs213485680 | in-del | -/A | | | intron-variant | Mid2 | Mm_Celera | X:140690174 | CTCATTTGTACATTC[-/A]AAAATCCTCAAAACA | 23947 |
rs213498068 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140757669 | TTTTGTAAATAGTTA[C/T]TATATTGTTAATGTT | 23947 |
rs213522837 | in-del | -/G | | | intron-variant | Mid2 | Mm_Celera | X:140708526 | ATGACCATCTGGAGA[-/G]GGGGGGGAAGGGAAT | 23947 |
rs213537621 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140695131 | AGTCATTATGAATAA[C/G]TAAATCCACATCCCC | 23947 |
rs213659095 | snp | C/T | | | upstream-variant-2KB | Mid2 | Mm_Celera | X:140663062 | CACTACTAGACGTAT[C/T]GCCCTTAGTTTCCTA | 23947 |
rs213678311 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140741015 | GATACGATATTCTGT[C/G]TCTTTGAGACAGGCT | 23947 |
rs213721844 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140700509 | CTGGAAGTTACCACT[A/G]TCTCAGTAGCACTTG | 23947 |
rs213761368 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140714201 | TGGCTTTGGTATTGC[C/T]GAATAGCCCAGGTTC | 23947 |
rs213790096 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140758172 | CACAAACACACACTA[C/T]ATTCACCCCAGAGAG | 23947 |
rs213812460 | in-del | -/T | | | intron-variant | Mid2 | Mm_Celera | X:140728599 | CTCCTCCTTGCCTTA[-/T]TTTTTTTAATGGGGT | 23947 |
rs213866505 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140726082 | AACATGGCCTACAGA[A/G]TCAACTAATCTGGGC | 23947 |
rs213914097 | in-del | -/ATA | | | intron-variant | Mid2 | Mm_Celera | X:140737320 | ATGGAAAGGAAAAGC[-/ATA]ATAACTGATAGAGAG | 23947 |
rs213930967 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140727267 | CTGCCTAGTTTAAAA[C/T]CCTGATTTTGACTCT | 23947 |
rs213987968 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140738901 | TCTCCATACTTCACG[C/T]GACCGACCTCCCTCC | 23947 |
rs214023357 | in-del | -/C | | | intron-variant | Mid2 | Mm_Celera | X:140713227 | GCCAACTGTCTCTGA[-/C]CCCCTCCCTAGTGCT | 23947 |
rs214036804 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140718335 | ACAGTGTGGAGGTCA[C/T]TGTGTTCTCGAATGG | 23947 |
rs214037528 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140740173 | AGTTGAACATTTTTC[A/C]TGATTATTGCTGCTT | 23947 |
rs214038120 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140729385 | TCACTCTGTTGCCCG[G/T]GCAATCTGATCTGCT | 23947 |
rs214055015 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140707526 | TGTATGTGGGTTCAT[C/T]TCTGGGTCTTCAATT | 23947 |
rs214055669 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140708397 | CCACACTATGGTATA[A/G]GGTATAGTATAGAAA | 23947 |
rs214070811 | in-del | -/T | | | intron-variant | Mid2 | Mm_Celera | X:140691043 | TTAGAGAACAAAGAG[-/T]GGATTTTGATTTACA | 23947 |
rs214098621 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140719512 | ACCTTCCAGTAGAGA[C/T]TGCTGGCTCTGAATG | 23947 |
rs214107323 | in-del | -/T | | | intron-variant | Mid2 | Mm_Celera | X:140697602 | ACTCCCCCCCCCCAA[-/T]TTTATCTTATCCAGA | 23947 |
rs214162583 | in-del | -/CACCAC | | | intron-variant | Mid2 | Mm_Celera | X:140719968 | TCTGATCCATTCTGT[-/CACCAC]CACCACCCTGCCCCT | 23947 |
rs214163481 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140715978 | TGAGGGTGTTCCCCA[A/G]CCCACCCATCCACTC | 23947 |
rs214215644 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140728711 | TCTCAACACTAGCCC[C/T]GAGAGTGCCCACCAC | 23947 |
rs214252418 | in-del | -/TT | | | intron-variant | Mid2 | GRCm38.p3 | X:140698766 | AGTTCTTCATTGCAA[-/TT]TTTTTTTTTTGAAAT | 23947 |
rs214253245 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140687880 | GGCAAGTATAGAGTC[C/G]GGACAGCTCTGTGCC | 23947 |
rs214283625 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140708859 | AATATCATTGTGAGT[C/G]AGGTAATCCAGTCAC | 23947 |
rs214299475 | in-del | -/TGTT | | | intron-variant | Mid2 | Mm_Celera | X:140681913 | GGAAGGTAGTTTGTC[-/TGTT]TGTGTGCTTGTTTGT | 23947 |
rs214346038 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140701178 | GAGGGAGGAAGGAGG[A/G]AGGGAGGAAGGAAGA | 23947 |
rs214362608 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140759369 | GCTGTTTTTGTTTTT[A/T]AAATTTTTGAGAGAC | 23947 |
rs214418656 | snp | G/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140708055 | GTAGAATTGCAAGCT[G/T]GTACAACCACTCTGG | 23947 |
rs214438198 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140716628 | ACAGAAACAGCACAT[G/T]AAACTCCTCAAAAGA | 23947 |
rs214450435 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140678951 | AGTCTTTCTCATCTG[C/T]GACACATTGTGCATT | 23947 |
rs214465940 | in-del | -/AAAA | | | intron-variant | Mid2 | Mm_Celera | X:140684718 | GATTCTAAATTAGGC[-/AAAA]AAAAAAAAAAAGTCT | 23947 |
rs214509853 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140679605 | CAGATGTAGCCAACT[A/G]TTGGTTTCCTATTGC | 23947 |
rs214522935 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140666281 | CACTTTGATTTTTTT[G/T]GAAGATTTTGGAGGG | 23947 |
rs214535024 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140690158 | AAGCAAATAGGTACA[C/T]ACTCATTTGTACATT | 23947 |
rs214562347 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140742484 | GGAGGCAGAGGCAGG[C/T]CGATTTCTGAGTTTG | 23947 |
rs214583617 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140674460 | ATGATTTTTCTATGT[C/T]GTAATATAGCTTTCT | 23947 |
rs214592918 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140675486 | ACCTGGGTAGTTTTC[A/G]ACACAGGCATTGTGG | 23947 |
rs214618259 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140750340 | CATACACTGTAAATT[A/G]ATTTTGTATCATTAT | 23947 |
rs214765918 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140717986 | ATTTCTTTTAGATTC[C/T]AGCGAATATCTTTTG | 23947 |
rs214790573 | in-del | -/AAC | | | intron-variant | Mid2 | Mm_Celera | X:140715652 | GACCTTGTTTCAATA[-/AAC]AACAACAACAACAAC | 23947 |
rs214806565 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140755521 | GCTGCATAATGGGAC[C/T]CTTGTCTCAAAAAGT | 23947 |
rs214819351 | snp | C/T | | | utr-variant-5-prime, intron-variant | Mid2 | GRCm38.p3 | X:140665152 | TGGTGGCGGCGGCGG[C/T]GGCGGCAGCAGCGAC | 23947 |
rs214840401 | in-del | -/G | | | intron-variant | Mid2 | Mm_Celera | X:140760137 | CCAAAGAGAAAAAAA[-/G]GAAGAACCCATCAGA | 23947 |
rs214855239 | in-del | -/T | | | intron-variant | Mid2 | Mm_Celera | X:140756225 | TACTCATGATCTTGC[-/T]TCTCTCCAGTCTTTA | 23947 |
rs214855552 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140741903 | TTACAGACTCTTGCT[A/G]TTACTTTTGGTTACC | 23947 |
rs214865817 | in-del | -/GCTATATAT | | | intron-variant | Mid2 | Mm_Celera | X:140711070 | TTTGATGATAATATA[-/GCTATATAT]TTTTATTTAGTTATA | 23947 |
rs214909717 | snp | C/T | | | utr-variant-5-prime, intron-variant | Mid2 | Mm_Celera | X:140664703 | TTGCTCGGGTTTCTC[C/T]GGTCACTCCTGCCAG | 23947 |
rs214961258 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140753372 | ATCCTCAGTCAATGG[A/G]TTATATTTCTTATAC | 23947 |
rs215017236 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140753241 | TGGGTCTTCTGTCAC[C/G]ACAGCCTGAGTGCTG | 23947 |
rs215017357 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140741092 | GTCATCAAATACTGG[A/G]CAATAATCCTGCCTC | 23947 |
rs215038628 | snp | A/G | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140676474 | AATTTACTGTAGGAC[A/G]TTCATTAAATACCTG | 23947 |
rs215044238 | in-del | -/A | | | intron-variant | Mid2 | Mm_Celera | X:140738879 | CCTATCCCCCATGCT[-/A]ATTTTTTCTCCATAC | 23947 |
rs215057599 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140711284 | TAAAATGCAGCTGGA[A/G]AAAGCTTTTGATTTA | 23947 |
rs215064864 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140700368 | TGAGGAAATACAGAA[A/G]GAGTTCTTTTTAAAG | 23947 |
rs215075412 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140703755 | GTCCTTCTGCTAAAG[A/G]CTGGGCATGACGACA | 23947 |
rs215104371 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140706287 | GTTATACTTAGTAAG[C/T]GCCATATATGGAATG | 23947 |
rs215140636 | snp | A/G | | | intron-variant | Mid2 | GRCm38.p3 | X:140707916 | CTTAGTCATCAGGGA[A/G]ATTTAAATCAAAACA | 23947 |
rs215156332 | in-del | -/A | | | intron-variant | Mid2 | Mm_Celera | X:140673110 | CTGGAAAAAAAGTAG[-/A]AAAAAAAAAGAAGCA | 23947 |
rs215193547 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140697151 | GGTTAGTTTAGGATT[A/T]TGTCCTGAATGAAGT | 23947 |
rs215195245 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140744337 | CAATCAACTGCTCTG[C/T]TGATGATTCCAAATC | 23947 |
rs215245751 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140727688 | ACCACCAAGGACCTA[A/T]GGCTGTTAGAATTGT | 23947 |
rs215285084 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140667818 | ATCCAAGCAGTGTCC[G/T]GAGTGGTGAGCCTTT | 23947 |
rs215286644 | snp | A/C | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140676217 | ATGTTTAATTTGACT[A/C]TCAGATGAAATTATC | 23947 |
rs215365898 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140754909 | TGTGCTGGTCCCATC[C/G]CACCAAGTCTTATTG | 23947 |
rs215438428 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140709541 | AGGAATGGGAGGGTT[C/G]GTGAGCAGGGGAAGG | 23947 |
rs215449586 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140701552 | TTTCAGCTCTTAAGT[A/T]AAGTAGTTTTTATTT | 23947 |
rs215457370 | in-del | -/AA | | | intron-variant | Mid2 | Mm_Celera | X:140705342 | TCCATATTTTGTACT[-/AA]AAAAAAAATAATAAA | 23947 |
rs215481178 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140703022 | CTATGACAACTACCA[C/T]GCACACACAGCTGTC | 23947 |
rs215491995 | in-del | -/T | | | intron-variant | Mid2 | Mm_Celera | X:140713415 | CATATCTTTCACCTC[-/T]TTGTCCTTTCTTCTG | 23947 |
rs215527954 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140685270 | ATTCTTTGTCTCAGT[C/T]GATGATATAAGAAAC | 23947 |
rs215677973 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140710685 | TGCTTTCTGTTTCAC[C/T]GATTTAATTTTTAAT | 23947 |
rs215711058 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140758374 | TGCAAGCCTGGAGCC[C/T]TGAGCACAGCTTGCA | 23947 |
rs215711599 | in-del | -/AGACATGCTTTCT | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140676776 | CAGTTTCATCCAGGG[-/AGACATGCTTTCT]ATTTGTCCTTAGTGA | 23947 |
rs215747300 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140731514 | ATAAAATCATTTAGC[C/T]AAGCCCACTAACTCG | 23947 |
rs215780610 | in-del | -/T | | | intron-variant | Mid2 | Mm_Celera | X:140761763 | TTTTGTTTGTTTGTC[-/T]TTTTTTTTAACTTCC | 23947 |
rs215785783 | snp | C/T | | | missense | Mid2 | Mm_Celera | X:140763107 | ACTGGGAGGTGGTCA[C/T]GGGTTCTTCAACATG | 23947 |
rs215786112 | in-del | -/T | | | intron-variant | Mid2 | Mm_Celera | X:140684155 | AAAAATGAAAAAAAA[-/T]GTTGGGATTTATGTT | 23947 |
rs215789916 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140728518 | ATAAGCATGTATATG[A/T]TACATGTACATGTAT | 23947 |
rs215796237 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140667695 | TATCATCTGAACAGC[A/G]CAAATTGACTTAGAT | 23947 |
rs215834730 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140689948 | CATTTGACAGTGATC[A/G]GTCTTTTCCTGAAAC | 23947 |
rs215856259 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140675309 | GTTTCCCTAAGTTTA[A/T]TTTCATAGTGAGGTT | 23947 |
rs215869813 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140742787 | GCTGTCCTGGAACTC[A/C]CCATGTAGACCAGAC | 23947 |
rs215879113 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140666525 | GCTAAATGGAGAGTT[C/T]ACATTCTTGCTCACT | 23947 |
rs215931107 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140744272 | TCTCTCCCCACACAG[C/T]TTTCCTTACAAACCC | 23947 |
rs215940052 | in-del | -/CAAT | | | intron-variant | Mid2 | Mm_Celera | X:140681626 | AAGCTATGGGGGAGA[-/CAAT]CTAAGCACTTTCCCC | 23947 |
rs215958967 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140737149 | TACAAAAAGTGTTGT[A/G]AAACTATTATGATTC | 23947 |
rs215980044 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140759008 | ATTGATAGAGTTTTA[C/G]TTTTTGCACTTATTT | 23947 |
rs215995113 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140719383 | TGCCTTTTCTGAACA[C/T]GGACCGAGGATTTTC | 23947 |
rs216032751 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140686431 | TCCACCTGTTTAAGC[C/T]AAATATTTACTGAAC | 23947 |
rs216134933 | snp | A/T | | | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140735477 | CTTTTGGTACTTAAT[A/T]AAGCATTATGACAAG | 23947 |
rs216166430 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140692809 | TTTTTAGGCACTTGC[G/T]TTGCATGTGTGAGGC | 23947 |
rs216201746 | in-del | -/TTT | | | intron-variant | Mid2 | Mm_Celera | X:140700017 | AAATATCCAATAAAC[-/TTT]TTTTTTTTTTAAATA | 23947 |
rs216222866 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140754395 | AGACGTTTCCCCCTG[A/G]ATTCTGAGTGTTCCT | 23947 |
rs216244285 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140705695 | TTACATGTATTATTT[C/T]ATTTAATCCTCTCAA | 23947 |
rs216268815 | snp | A/G | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140677295 | CAGCTTATTAGAGAT[A/G]GGATAAAACAGATTT | 23947 |
rs216282460 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140712309 | TATGTATAGTTCTTA[A/G]TATATCTCCTTTCCA | 23947 |
rs216300365 | snp | A/G | | | utr-variant-3-prime | Mid2 | Mm_Celera | X:140767391 | AGCCTTAGAGCCATT[A/G]GGCTGTATTTGGCTG | 23947 |
rs216325757 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140710849 | TAATCCAGTCCAGCC[A/T]CACCTACACAGGGAA | 23947 |
rs216327588 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140720818 | AACACCAAGCCAACA[A/G]CCATAACATATGTGC | 23947 |
rs216364576 | snp | A/G/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140717518 | tatatgtatatgtat[A/G/T]tgtatatgtatatgt | 23947 |
rs216390133 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140761709 | AAAACCGACAAGAGT[C/T]CTAGCGAGATTTCCA | 23947 |
rs216450982 | snp | A/C/G | | | intron-variant | Mid2 | Mm_Celera | X:140722014 | AAACTAGACATAAAA[A/C/G]GAACCCCAAACAATC | 23947 |
rs216504311 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140719678 | ACTTTCCATTACTTG[C/T]CCTGTCTTTCCCTCC | 23947 |
rs216520262 | in-del | -/TCTGTCTCTCTCTCTCTCTCTCTCTCTCTC | | | intron-variant | Mid2 | GRCm38.p3 | X:140681695 | GGGAAAGAACTATTG[lengthTooLong]TCTCTCTCTCTCTCT | 23947 |
rs216541358 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140665484 | GCAATGGCAGGGCCC[C/T]GGTTGTCTGTCACAC | 23947 |
rs216542847 | snp | C/T | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140677155 | AGCTGGAGGGGCACT[C/T]GGTACAGATTAAGTC | 23947 |
rs216598260 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140666408 | TGGGGATTAATTAAT[C/T]TGATTCTCGAATTGG | 23947 |
rs216659692 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140761670 | TACCACAGAGAAGCC[A/G]TAGTTTTAGGAGTGC | 23947 |
rs216670978 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140753977 | CTAGAACTTACTTTT[C/T]CCCTTTGTCCCTTCT | 23947 |
rs216676439 | in-del | -/TGCC | | | intron-variant | Mid2 | Mm_Celera | X:140712334 | TTCCATTGTTAGTAT[-/TGCC]TGCCTGCCTGCCTGC | 23947 |
rs216691882 | in-del | -/CCTGT | | | intron-variant | Mid2 | Mm_Celera | X:140719235 | TCACTCTTGACCTGA[-/CCTGT]CCTGTCCAGCTCCGA | 23947 |
rs216737611 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140680621 | CTGTTTAGTAATTGC[A/T]CTGGCACTGAAAAGC | 23947 |
rs216737658 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140668749 | GTTAGTGCCCTTTCC[C/T]ACTTCTCACCTTCAA | 23947 |
rs216790427 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140669750 | AATGGATGAAAATTT[G/T]CACTAGTAGCCTAGG | 23947 |
rs216804102 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140723959 | TGTGTATGATGTTTT[A/G]CCTGCATTCATATCT | 23947 |
rs216811411 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140679882 | AAATGTTAAATGTCT[A/C]GGGACTTTTGGAAAA | 23947 |
rs216822498 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140755568 | CTCTTATATAGCCTC[C/T]CATTTGCATTCTAGG | 23947 |
rs216836677 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140745729 | CTGAGGTGTATGGAT[A/C]CAGAAGGATTTTTTA | 23947 |
rs216846179 | in-del | -/GCG | | | utr-variant-5-prime, intron-variant | Mid2 | GRCm38.p3 | X:140665085 | GATCCCGGCTGTTGC[-/GCG]GCGGCGGCGGCGGCG | 23947 |
rs216852667 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140670040 | TATTCATTTTAATAT[A/T]TATGATGATTGAATT | 23947 |
rs216936010 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140711485 | ACTGGAAAGAGCCTT[C/T]GCGTGTTGCCATTTA | 23947 |
rs216945685 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140755020 | CACTTGATTAGTTCC[A/C]CACCACTGAGAGACT | 23947 |
rs217027115 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140721145 | GATTGGGCTAGACAC[C/T]GATCTCTGAATATCA | 23947 |
rs217056355 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140756146 | TGATGCTTTAAAATT[A/T]TACAAAATATCCTGC | 23947 |
rs217071437 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140756882 | GTGACCTCTGAATGG[A/C]ACATAGCTTTAAAAA | 23947 |
rs217141344 | in-del | -/CA | | | intron-variant | Mid2 | Mm_Celera | X:140703947 | GTGAATACATGTGTG[-/CA]TGTGTGCGTGTGTGT | 23947 |
rs217153186 | in-del | -/TCTTGTGAGTAAGAG | | | intron-variant | Mid2 | Mm_Celera | X:140681350 | CACACACACACACAC[-/TCTTGTGAGTAAGAG]ACACTCTTGTGAGTA | 23947 |
rs217162468 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140680816 | GTGGGAGTAAGAAGA[C/G]TGGGGGATATGGAGA | 23947 |
rs217205865 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140723501 | CACCTGCCTCTGCCT[C/T]CCAAGTGCTGGGATT | 23947 |
rs217234962 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140706748 | CTGTAAGTCTAGCTC[C/T]AAAGCATCCAATGCC | 23947 |
rs217312098 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140714132 | GTAAGTGTTACCACC[A/G]TGGTTCTCTTTCCTG | 23947 |
rs217388003 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140708194 | ACATACTCCACTATG[C/T]TAATAGCAGCCATAT | 23947 |
rs217428090 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140747594 | GATGAGTAAAAGAAG[A/T]TTGGGAAGGCCAGGA | 23947 |
rs217464574 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140680025 | ACATATTTAATTATG[C/T]GTTCATTATAAAATA | 23947 |
rs217468827 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140715215 | TCACCTAGCCAAATA[A/G]AGGCAACCCAGACTT | 23947 |
rs217496887 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140673481 | GGAATTTCATATAAA[A/T]GGAATCACACAATAT | 23947 |
rs217566253 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140672388 | TCCTTCCCCTCTCTT[C/T]CTACTTCTTAAAAAA | 23947 |
rs217568516 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140740028 | ACATTCCCACTATCA[G/T]TATATAAGGGTTTTC | 23947 |
rs217587467 | snp | A/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140667002 | ATTGGGTTACTGGAT[A/T]GACTGGGTATAAATG | 23947 |
rs217598168 | snp | G/T | | | utr-variant-3-prime | Mid2 | Mm_Celera | X:140765881 | AAGCTTTAGTTCCCC[G/T]TTCTACTATGGACTG | 23947 |
rs217606705 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140755601 | TGACAGTTAGTTCAA[C/T]AATATTGATTATAAT | 23947 |
rs217635009 | in-del | -/T | | | intron-variant | Mid2 | Mm_Celera | X:140712402 | TCCTTCTTTTCTTCA[-/T]TTTTTGAGACAAGAT | 23947 |
rs217657462 | in-del | -/G | | | intron-variant | Mid2 | Mm_Celera | X:140743402 | GGGGGTGTATATGCA[-/G]GGGGCGGGGGAGGAG | 23947 |
rs217663339 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140738880 | CTATCCCCCATGCTA[A/T]TTTTTTCTCCATACT | 23947 |
rs217667215 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140719359 | ttgttttgttttCTA[C/G]TGGTCCCCTGCCTTT | 23947 |
rs217670650 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140692057 | GAAAGTAAAATATAC[C/T]GAGACTACAGGAAGC | 23947 |
rs217674536 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140679186 | TGCGGCTCAGTGATA[C/G]AGTGCTTACATAGCA | 23947 |
rs217683396 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140680130 | ATAAGCCAGGCTAGA[A/T]GGAAGGTCCCAGTAG | 23947 |
rs217685145 | in-del | -/AGGCACT | | | intron-variant | Mid2 | Mm_Celera | X:140723297 | TACCTACAGTATGTC[-/AGGCACT]AGGCTACATGTTGTG | 23947 |
rs217750967 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140731442 | GTTTGCAGAATTACC[C/T]CAGTGGTATCTTCAA | 23947 |
rs217763069 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140747940 | CTCAGCACTAAGGAG[A/G]TATTAGAAGAGGATC | 23947 |
rs217784100 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140748531 | TTATGTGTGATCTTG[A/G]CAGCCTACTTAGCTT | 23947 |
rs217796226 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140690470 | ATTACTATGTTGTTC[A/T]GTACATAGTAACTGA | 23947 |
rs217886924 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140755800 | ACAAGAAGTTTGATT[C/T]AGGAGTATTATAGCT | 23947 |
rs217934403 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140688802 | AATCCCGTGGCCAAA[A/G]CAATCACATCATTCA | 23947 |
rs217963054 | snp | A/G | | | utr-variant-3-prime | Mid2 | Mm_Celera | X:140766179 | CAAGCTTCTCAGGTT[A/G]TTCTGAATCACACAA | 23947 |
rs217966138 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140755276 | AACTGACAAGCCCTG[A/G]ACTCTGACAGGCCCG | 23947 |
rs217980851 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140742035 | GTGGCACAAGTTCTG[C/T]GGCTATAACCAATCA | 23947 |
rs218047649 | in-del | -/TCCCCTTTCTTTC | | | intron-variant | Mid2 | Mm_Celera | X:140690829 | ATTGCTGCCGTTTGT[-/TCCCCTTTCTTTC]TCCCCAATCCCTTCT | 23947 |
rs218100530 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140712807 | TTTGATTTTTTTAGA[C/G]TTATCTAAGAGCCAG | 23947 |
rs218100579 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140723527 | GGATTAAAGGCGTGC[A/G]CCACCACTGCCTGGC | 23947 |
rs218127057 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140720248 | AGTGATGGACATAGA[A/C]CTTGTCTACGCAGGA | 23947 |
rs218153100 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140713631 | ACAAAAATAGAACAA[C/T]ACACTGGTGGGGCTT | 23947 |
rs218158656 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140733646 | ACTGATTGAGCATAT[C/T]GTATTTAGGAACACA | 23947 |
rs218176147 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140721290 | TAATGGAATGGCCTT[C/G]AATTAGACCAGTCAC | 23947 |
rs218178667 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140722909 | CCTTCAGTATCCATG[A/G]AGGATTGGCTCAGAT | 23947 |
rs218409716 | in-del | -/CCT | | | intron-variant | Mid2 | Mm_Celera | X:140700825 | ATCATGCAAGCTCAA[-/CCT]CCCCTTCCCGACTTA | 23947 |
rs218437861 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140691509 | CACTCCCTATGGGCC[C/T]ATGAGACCATTTTTA | 23947 |
rs218438926 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140690219 | CCCCCCGACCTAAGA[C/T]AGGTTCTACTTATGT | 23947 |
rs218472031 | snp | G/T | | | utr-variant-3-prime | Mid2 | Mm_Celera | X:140765534 | AAGATTATATGTACC[G/T]TATAGCTCATTAGGA | 23947 |
rs218491576 | in-del | -/A | | | intron-variant | Mid2 | Mm_Celera | X:140687027 | TATCTAGATAGGATG[-/A]AAAAAAAGGGTGATG | 23947 |
rs218553569 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140725579 | TTCTGTCTGCAAGCA[G/T]AACAGAGTATCATTA | 23947 |
rs218586765 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140763463 | ATAAAAGTTTCTGTC[G/T]TCTCCACTGTCTTAG | 23947 |
rs218598551 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140756612 | AGGAGCCCTGGCTAT[G/T]TTTAGTAGGACAGTG | 23947 |
rs218616209 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140703852 | GTTGCCTCAAGTATA[C/T]GTAATATTATAACGT | 23947 |
rs218637388 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140673692 | ATGAATATTGCTGCT[A/G]TGAACATTGGTGTTC | 23947 |
rs218655326 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140757002 | GTTGTGAGCCACCAT[A/G]TGGTTGCTGGGATTT | 23947 |
rs218668715 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140725014 | ACTTCCTGGCTGCAT[C/G]TATGTATTCTTACTT | 23947 |
rs218708309 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140695788 | TGGAGTAATAGATAA[C/T]AGTGAATAAAGTGAG | 23947 |
rs218720726 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140694938 | GATTTCTCATGGGCA[G/T]TGATTGGGCCATTTT | 23947 |
rs218726504 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140674781 | GAGGTAGGGAAATGG[A/G]GACTAGTTTCAGGCA | 23947 |
rs218734694 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140675690 | AGGAGGTGAGATGAT[A/G]GAATAAAGGTGTAGG | 23947 |
rs218742868 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140682400 | CACATTCACCAGTGT[C/T]GTTCTCTTGGCTTGC | 23947 |
rs218747600 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140682843 | TTAGTAGACATAAAT[C/T]ATTCTTGCCATTATG | 23947 |
rs218753678 | snp | A/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140708706 | CCCACTATTGCCAGG[A/T]AACTGTGGGGTGGAG | 23947 |
rs218783268 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140687201 | gtgtgtgtgtgcgtg[C/T]gtgtgtgtgtgtATT | 23947 |
rs218808124 | snp | C/T | | | downstream-variant-500B | Mid2 | Mm_Celera | X:140768073 | CTTACTGTTAAACAT[C/T]TGGACTGTAGGAGGA | 23947 |
rs218850028 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140685636 | CTCCACGAGGAAAGG[A/C]CTGAATAGGACTTAA | 23947 |
rs218853332 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140693430 | ATGGTATGAGAGCCA[A/T]CCAGGAAGTGATCCT | 23947 |
rs218870687 | in-del | -/TT | | | intron-variant | Mid2 | Mm_Celera | X:140754874 | TGACTATGAAGTGTA[-/TT]TTTTTTTTTACATTA | 23947 |
rs218871419 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140681673 | AACAGTAAATTCTGT[A/C]AGAAAAGGGAAAGAA | 23947 |
rs218888694 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140723926 | AAAAATTAGATTTAG[G/T]TATTTATTTCTACTT | 23947 |
rs218906287 | in-del | -/CCTGTTG | | | intron-variant | Mid2 | Mm_Celera | X:140674202 | ACAACAACAACAAAA[-/CCTGTTG]TCTAATCTAAAGCAT | 23947 |
rs218947559 | in-del | -/A | | | intron-variant | Mid2 | Mm_Celera | X:140727667 | AAAAACAAAGCAAAC[-/A]AAAAAACCACCAAGG | 23947 |
rs218959190 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140752573 | ATTTGATTTCTGGAC[C/T]GCTATAAATGATCTC | 23947 |
rs218982313 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140758638 | TCAAGACCACCCACT[C/T]CTAACTCATCTCCAC | 23947 |
rs219036182 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140751441 | CCATTGCTTCCTTTA[C/T]TCTACCTATTTGTGT | 23947 |
rs219043377 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140722580 | AGCACTGTTAAGAAA[A/T]CGATGATTAAGTAAA | 23947 |
rs219134013 | snp | A/T | | | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140735207 | CAGAGAACTCTTTTC[A/T]GTTACCAGATGCTAC | 23947 |
rs219181663 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140715353 | TCTTCCTGTTCACCC[A/C]CATGACTGTGTATGT | 23947 |
rs219217174 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140723460 | GGCTCACTCTGTAGA[C/G]CAGGCTGGACTCAAA | 23947 |
rs219233792 | in-del | -/CT | | | intron-variant | Mid2 | Mm_Celera | X:140739280 | TCTTTACATATTCCC[-/CT]CTCATTCATTGAAGA | 23947 |
rs219268995 | in-del | -/TGGGTACT | | | intron-variant | Mid2 | Mm_Celera | X:140680168 | AAGGCGGGAAAGTAA[-/TGGGTACT]TGGGTACTTTTCTTC | 23947 |
rs219375748 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140725958 | AAAGGGCATATTGAT[A/G]GAAACAGATGCAGCA | 23947 |
rs219381446 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140736626 | TGATTGCAGTTTGGA[A/G]TTGAAAAATAAAATC | 23947 |
rs219429082 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140698388 | AGTAAGAAGAGAAGA[A/G]TATAAAGCAGCGAGC | 23947 |
rs219433944 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140684521 | CCATCAAAACCAAAT[A/T]AAAAAAACATAAAAG | 23947 |
rs219439613 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140725303 | CATGAAGACCAAGCT[A/G]CACATTTGCTGCATA | 23947 |
rs219445629 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140685432 | CTTTGTCACAATTGG[A/G]GCTTTGAGCTTAGTA | 23947 |
rs219451184 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140693523 | TTAGGGTAGGGTGAT[A/G]TGCACTCAATAGCCA | 23947 |
rs219538219 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140696542 | TCTTTTTATTATTTG[C/G]TCTGCTCTTTTGATA | 23947 |
rs219539292 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140683925 | AACCTACCCTAAAGC[C/T]AGGCCATACATGGTT | 23947 |
rs219563728 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140757626 | TAAGTCATTTCTAGA[C/T]TATTTATAGTGTCTA | 23947 |
rs219572408 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140692344 | GTGATTGAAATTCTT[A/C]GTGTCTATCGAAAGA | 23947 |
rs219629431 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140737351 | AGAAAATGATCTTAT[C/T]CAACTTATTAGCTAC | 23947 |
rs219710240 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140668190 | GTATTGACTTTTTGT[C/T]CTGTCTTCTGTGCAA | 23947 |
rs219836289 | in-del | -/GGTGGGG | | | intron-variant | Mid2 | Mm_Celera | X:140665905 | TGAAAGCAGCCCCGT[-/GGTGGGG]GGGGGGGGGGGGGGT | 23947 |
rs219849774 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140727841 | AAATCAAAAGGAAAA[C/T]ACCAGGTATATTGGA | 23947 |
rs219866814 | in-del | -/GTGTGGG | | | intron-variant | Mid2 | Mm_Celera | X:140705944 | GGAATTAATGTGTGT[-/GTGTGGG]GGGGGGGCAGAAGTG | 23947 |
rs219869324 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140724898 | TTTCTCTGTGTACCC[A/C]TGGCTGTCCTGGAAC | 23947 |
rs219919735 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140725482 | CTATAAGAGTCCCCA[A/C]GCTCCTTCCACTGTT | 23947 |
rs219921409 | in-del | -/TGTC | | | intron-variant | Mid2 | Mm_Celera | X:140666324 | ATGGCATTAGTTGTG[-/TGTC]TGTCTCTAAGGAGGA | 23947 |
rs219934680 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140726717 | CTGAAGAGACACAGC[A/G]GAGGAATGGATGGGC | 23947 |
rs220030740 | in-del | -/A | | | intron-variant | Mid2 | Mm_Celera | X:140684148 | ACTTAAATAAAAATG[-/A]AAAAAAAGTTGGGAT | 23947 |
rs220113156 | in-del | -/TG | | | intron-variant | Mid2 | Mm_Celera | X:140687799 | GGTGTTAAGACTGGC[-/TG]TGTCTGGTCCATGTG | 23947 |
rs220142299 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140711128 | TTCATACACACAGAC[A/C]CACACACATATATAT | 23947 |
rs220154656 | in-del | -/TTTATGCATG | | | intron-variant | Mid2 | Mm_Celera | X:140728739 | CACCATGCATGGCTT[-/TTTATGCATG]TTCTAGGGATCCAAA | 23947 |
rs220169727 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140711495 | GCCTTCGCGTGTTGC[C/T]ATTTAGTATGATATT | 23947 |
rs220321552 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140730394 | CTTCTGAACTCCTGC[A/C]CAACTCTCTATAGGA | 23947 |
rs220322482 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140759767 | AGCCTTGCCTGAGCC[C/T]AGAAGTTGCTCTATA | 23947 |
rs220385828 | snp | G/T | | | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140735592 | GATATTTTAATACAT[G/T]AACTACTGCTACTGT | 23947 |
rs220394565 | in-del | -/GCGCGCGC | | | intron-variant | Mid2 | Mm_Celera | X:140718907 | GGGTGATATGCGCGC[-/GCGCGCGC]GCGTGTGTGTGTGTG | 23947 |
rs220413508 | snp | A/G | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140677360 | AGTCTGGAGGAAAAT[A/G]TATTATTCCGCTCTG | 23947 |
rs220460253 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140728875 | CTCATGGTGCCCTTA[A/G]TCTCAGAAACCTCCT | 23947 |
rs220537638 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140693557 | TTCCCTCTCATCACT[A/C]TTTCCCCACTGCCTA | 23947 |
rs220614899 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140739502 | CACTTAAAATCACAG[C/T]CATAAGTTAAAGCAT | 23947 |
rs220616045 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140750527 | TGCTATCTATAGATG[C/T]ATTTTTACAAGCATT | 23947 |
rs220727985 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140748144 | AAAGCTATTGTTTGT[A/C]GATCTGCAACAGAGC | 23947 |
rs220736413 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140749439 | AATGGAAACTGTTTC[C/T]GTTAGAAAGGCAGAG | 23947 |
rs220739691 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140708625 | AATAAAAGAGGGCAA[A/G]CAACCCCTCTTATTG | 23947 |
rs220788698 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140749044 | ATGTGAAAATTATTT[C/T]AAATAAATACATAAA | 23947 |
rs220799993 | snp | C/T | | | upstream-variant-2KB | Mid2 | Mm_Celera | X:140664197 | CCTGAACAACTTGTG[C/T]CCAAGTCCAATAGAA | 23947 |
rs220803543 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140739433 | AGACTTCCAACTCAG[A/G]TCACTCACTTCCTAG | 23947 |
rs220821254 | in-del | -/TAA | | | intron-variant | Mid2 | Mm_Celera | X:140745770 | CTTCCAGTAAACATT[-/TAA]AAAAAAAAAAGCTCC | 23947 |
rs220853029 | in-del | -/TGG | | | intron-variant | Mid2 | Mm_Celera | X:140740565 | TTTATCCTAGTCTGT[-/TGG]CTATCTCTTCACTCA | 23947 |
rs220876068 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140669171 | TGATGATGAACAGTA[C/T]CCTCTGGCTCTGCAT | 23947 |
rs220881003 | in-del | -/G | | | intron-variant | Mid2 | Mm_Celera | X:140683105 | AGCTGATAAAAACCA[-/G]GGGGGGGATGGAGGA | 23947 |
rs220898882 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140746002 | ACCACTTCTGAGAGC[C/T]GATGGTGTGCTTTCA | 23947 |
rs220906208 | in-del | -/A | | | intron-variant | Mid2 | Mm_Celera | X:140671285 | TGAGACTCACAAGGC[-/A]ATTCCCTTCCCCTTT | 23947 |
rs220908199 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140673949 | GTATTATTACAGCTA[C/T]TCTAGTGTGTTTATT | 23947 |
rs220918982 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140674598 | TTATAAATACACAGG[C/T]TTATTTCTAGAGGCT | 23947 |
rs220954521 | in-del | -/A | | | intron-variant | Mid2 | Mm_Celera | X:140748615 | CACTGTGGTAAGGAG[-/A]AAAATTAGATAATTT | 23947 |
rs221029870 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140672918 | GGTTGTAGATGTCTC[C/T]GAGCATTGCAAGACC | 23947 |
rs221063076 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140742079 | CAAAGGCCTGCTTCC[G/T]GAGATGGGAGCCATA | 23947 |
rs221098377 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140695222 | ATGAACATCTCTAGC[A/T]GTATAATCCCCACTG | 23947 |
rs221140213 | in-del | -/AAAAC | | | intron-variant | Mid2 | Mm_Celera | X:140670420 | TGAATAAATTGTTTA[-/AAAAC]AAAACAAAACAGAAC | 23947 |
rs221162301 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140689451 | GCAACAGGTTGCAAG[A/T]ACTTGTTCAAAAACA | 23947 |
rs221162772 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140752744 | GATTCCATTTTTATA[C/T]GAGAAATTGGTGCTG | 23947 |
rs221168542 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140704050 | GAATGAAAATGGGTG[C/G]TGGTGGTGAATTCTT | 23947 |
rs221170010 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140741439 | GAGTTGATCGACCAG[A/G]GGTTACACTGTTAAA | 23947 |
rs221243364 | in-del | -/TTTT | | | intron-variant | Mid2 | Mm_Celera | X:140695021 | AGAGATCTAGTTTTG[-/TTTT]TTTTTTTTTTTTTGT | 23947 |
rs221251471 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140700723 | ATATACATATGCAAT[A/C]TCCTAGCTGTTTATT | 23947 |
rs221298106 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140703215 | ATAGGTGACATCCCC[A/G]TTTTCAAGCAATGAA | 23947 |
rs221320066 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140709906 | GGAATGCCTATTTTG[A/T]CTGTGAAGTAGGAGT | 23947 |
rs221357079 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140748010 | GGTCAGCCTAAAGCA[C/T]ACCAGATTCTGTTAA | 23947 |
rs221365430 | in-del | -/ATGTATATGTAT | | | intron-variant | Mid2 | Mm_Celera | X:140717502 | ATATGTGTGAATGTA[-/ATGTATATGTAT]TATATGTATATGTAT | 23947 |
rs221371139 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140708519 | GGCCGGCCATGACCA[C/T]CTGGAGAGGGGGGGA | 23947 |
rs221415265 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140709130 | CATACAGTCACCAAA[C/T]CCAGACACTATTGTG | 23947 |
rs221415488 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140699911 | GGGTATGTGGGGGAA[C/T]ATCCCCATACAAGCA | 23947 |
rs221544154 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140734023 | AGCAGTAGGAGTTGC[C/T]GTTTTTAGGATTATC | 23947 |
rs221598749 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140732217 | ATTTTTGAGCAAAGA[A/G]TATATTAGTTATGTT | 23947 |
rs221603864 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140745887 | AGGTATGCAACACAT[C/T]TGGCTTGTTTTTGTG | 23947 |
rs221649763 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140687336 | ATTGAGGTTTGAACA[C/T]AGGACCTTGTACATG | 23947 |
rs221665560 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140672650 | CTAGAGAAAGCTTCA[C/T]GATTATCTCTCATTG | 23947 |
rs221667971 | snp | C/T | | | upstream-variant-2KB | Mid2 | Mm_Celera | X:140662310 | GTACGCTTTAAAGGA[C/T]GTTTCATTTCCTTCT | 23947 |
rs221756981 | in-del | -/G | | | intron-variant | Mid2 | Mm_Celera | X:140713802 | TATGTGTTATCCCAT[-/G]GGGGCTAGTATCCTG | 23947 |
rs221782852 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140728823 | CGTTTCCCCAGTTCC[A/G]TTTCTTTCTTTAATA | 23947 |
rs221791613 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140682529 | TGGTTTTTTTCTTCA[A/G]TATCCTTCTTTGTGT | 23947 |
rs221806138 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140709302 | AGGACTGAAGGAGCT[C/G]AAGGGGTTTGCATCC | 23947 |
rs221806196 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140718396 | AAAGGGTAAAAATGG[C/T]AAAAACAAATCATGC | 23947 |
rs221821617 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140756964 | GACACACCAGAAGAG[A/G]GCTTCAGATTTCAGT | 23947 |
rs221841154 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140709783 | GTGGGATGACCTCTC[A/C]GGAGGAAGTGCCAGT | 23947 |
rs221849419 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140747972 | AAGGTTCAAGGTCAC[C/T]CTCAGCTACATAGGA | 23947 |
rs221879287 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140730064 | CTAATTAGTTGTATT[C/T]ACACTTCATTCTTTC | 23947 |
rs221909975 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140696685 | AGGCAAGTGCTATAC[A/C]TCATAGCAACAAGCA | 23947 |
rs221957100 | in-del | -/T | | | intron-variant | Mid2 | Mm_Celera | X:140674313 | TTAGATTGAGGTGGG[-/T]TTTTTTTTTGTAACC | 23947 |
rs221961791 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140705167 | GATCAGTTTCTGAGT[A/G]GGGGTAGGTGTGTTG | 23947 |
rs222027521 | in-del | -/AC | | | intron-variant | Mid2 | Mm_Celera | X:140745433 | TATGGAATTTCTCAT[-/AC]ACACACACACACACA | 23947 |
rs222161712 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140743354 | TGAGTCTCTTTTTCT[A/G]GGAAGGAATCCTGCA | 23947 |
rs222227575 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140758479 | TTATAGAACTGCCAA[C/T]GTGAGGGCGGGAGGC | 23947 |
rs222274950 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140753803 | ATTCCCTTGTCTCTG[C/T]GTCCTGAGTGCTGGG | 23947 |
rs222306567 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140671320 | GTTCACTGGAAAGTT[A/T]GATAAATCTCCCTGA | 23947 |
rs222344049 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140747168 | TGGCACAGTGGCGCA[C/T]GACTTTAATCTCAGT | 23947 |
rs222376489 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140669262 | TGACAACTCTTCCTG[A/T]AACCTAAACTCCTAA | 23947 |
rs222447229 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140681428 | AGAGAAAAAGGGAGG[C/T]GAGGAATTTCCTCCA | 23947 |
rs222490498 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140756408 | GATTTAGAATTCTTT[A/T]GTACCTTCATTTTTC | 23947 |
rs222502260 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140707843 | GAGTTTCAAGATCGC[C/T]AGGGCTCCACAGAGA | 23947 |
rs222549197 | in-del | -/T | | | intron-variant | Mid2 | Mm_Celera | X:140759310 | AGAGCATCCTCAGTC[-/T]TTCTTTTACAACTAT | 23947 |
rs222651341 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140674095 | TTCTAGCCCTAAAGG[C/T]TTAAGTTTAGATGAA | 23947 |
rs222671048 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140749825 | AATAAGCTTTTTCTG[A/G]TACACGTAGTTTTCC | 23947 |
rs222682699 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140709254 | GCCAACTATTGGACT[A/G]AGCACAGAGGCCCCA | 23947 |
rs222708681 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140706470 | TTTGGAAACTCAGTC[C/T]GTAGTGCCTGTTTTT | 23947 |
rs222725653 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140707738 | AAATGTTCAATAGCC[G/T]GGTAGTGGTAGAACA | 23947 |
rs222748055 | in-del | -/G | | | intron-variant | Mid2 | Mm_Celera | X:140715054 | GATCCAAGGGAAACT[-/G]GATAGTCGCAAGTGT | 23947 |
rs222757558 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140758006 | AAAGAAATCTTTTTT[A/T]TAAAAACACATTAAA | 23947 |
rs222783621 | in-del | -/TTTT | | | intron-variant | Mid2 | GRCm38.p3 | X:140668877 | GCTACCTTTTTCATC[-/TTTT]TTTTTTTTTTCATGA | 23947 |
rs222826060 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140667947 | ATTGTCTCTGGTTGT[C/T]AGGTTTTCCTTAGAA | 23947 |
rs222919997 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140717280 | CAACTATTGGGGTGG[A/G]GAAAACAGGCTTACT | 23947 |
rs222932910 | snp | C/G/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140713775 | CCACTTGGTTAGGGT[C/G/T]TATACTGACAAATAT | 23947 |
rs222961079 | snp | C/T | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140677436 | CTCTCTCCATGCAGG[C/T]ACTTAGAAAGGAATC | 23947 |
rs222963914 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140714300 | TTTGGGATGACAGGC[A/G]CAATCCATCATGTCC | 23947 |
rs222972868 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140666955 | AAACCTCAGCATTAT[A/G]CTCTTCAATGAAAGC | 23947 |
rs222994949 | in-del | -/C | | | intron-variant | Mid2 | Mm_Celera | X:140691535 | TTTTATTTAACCCCA[-/C]CCCCCCAATAATACA | 23947 |
rs223002103 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140706400 | GCTACTTCATTCATT[A/G]CATTTTAGGACCATT | 23947 |
rs223038687 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140709709 | CAGGAACCGGGAAGA[A/G]CATTAAGTAAACAAA | 23947 |
rs223073504 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140674672 | CAAGTATGACCTTGG[A/T]CAAACTACTTTCTTT | 23947 |
rs223083504 | in-del | -/ACACACAC | | | intron-variant | Mid2 | Mm_Celera | X:140733656 | ATATTGTATTTAGGA[-/ACACACAC]ACACACACACACACA | 23947 |
rs223102280 | snp | A/G | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140676972 | ATTGAAAGTTTTCTG[A/G]CTGCTCACCTCACAA | 23947 |
rs223102532 | snp | A/G | | | synonymous-codon | Mid2 | Mm_Celera | X:140750850 | ATCTATCCGAGAAGA[A/G]CTCTGTACTGCTTCC | 23947 |
rs223114738 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140716445 | CTATTAGTTCATTTG[G/T]TTTTCACAACTACTT | 23947 |
rs223134208 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140747152 | AGAGTAGCTTCTAGC[C/T]TGGCACAGTGGCGCA | 23947 |
rs223216233 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140741112 | AATCCTGCCTCAGCC[C/T]CCTAAGTGCTACGAT | 23947 |
rs223225481 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140731330 | GGGCCTGGCCAGGGC[C/T]GCCTGGGTACCTAGA | 23947 |
rs223260452 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140755822 | ATTATAGCTCAAGAC[C/T]TGCCTGGGCTACATA | 23947 |
rs223264938 | in-del | -/CATC | | | intron-variant | Mid2 | Mm_Celera | X:140753080 | TGCTTTTAAAACATG[-/CATC]CATCGTGTCAAAAGG | 23947 |
rs223272172 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140746066 | GAGGCAACAAACACC[G/T]TGACTCATTGCCCAT | 23947 |
rs223273207 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140756297 | TCCCATACTTACAAA[A/C]TGTCACTCGATATTT | 23947 |
rs223314396 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140665842 | CTCCCTGCTGGGGAA[A/C]CGATCTTCAGGTCTC | 23947 |
rs223318490 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140705113 | CATTGCCAAGTTCTG[A/T]GCTAACCTGGTGACA | 23947 |
rs223322311 | snp | A/G | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140677867 | GATTAATTTTCGAAT[A/G]ATCCCTATTGCTTAA | 23947 |
rs223338236 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140742215 | TTATAATGACTCCCA[A/G]TGAGTTATTGCTATG | 23947 |
rs223405099 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140689548 | GCTTTTTTTCTTCTC[C/T]GGGGTTTTCAATCAA | 23947 |
rs223405262 | snp | G/T | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140677066 | GAGACGAGGTTTTTT[G/T]TTTGTTTGTTTGTTT | 23947 |
rs223436314 | snp | A/G | | | intron-variant | Mid2 | GRCm38.p3 | X:140709503 | TGATGTCCCAGTGTG[A/G]GGGAATGCTAGGGTG | 23947 |
rs223445953 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140716971 | CAGCTTACGTTGGAA[C/T]CAACACTAACAAGCT | 23947 |
rs223455085 | snp | C/T | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140676913 | CACCGTCAGTTGGGG[C/T]GTTTCTTTTACTCTC | 23947 |
rs223480251 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140666664 | GCTATTTTTATATAT[C/T]CCTGCTCAATCAATT | 23947 |
rs223483241 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140712428 | AAGATCTCAGATGTA[G/T]TAATGGCTAGCCTGT | 23947 |
rs223483288 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140704370 | AAGCCCTGTTCACCT[C/T]CTCCTCACTAAAATC | 23947 |
rs223498847 | snp | C/G/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140753701 | TCAGACTACAGCGAG[C/G/T]AATTTGTTTTAGACG | 23947 |
rs223549400 | snp | C/T | | | utr-variant-3-prime | Mid2 | Mm_Celera | X:140766783 | ATTTACTTCAGTAAA[C/T]TTAAAAGACTTTCAT | 23947 |
rs223551765 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140755534 | ACTCTTGTCTCAAAA[A/C]GTTAACAACCATATA | 23947 |
rs223583525 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140690196 | CTCAAAACAGGGCTT[C/T]CCCCCCACCCCCCGA | 23947 |
rs223599905 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140755994 | CTTCTTAGAATGTCA[C/T]ATCCAGAGGTATGTA | 23947 |
rs223618343 | snp | A/G | | | utr-variant-3-prime | Mid2 | Mm_Celera | X:140765234 | TAGCCTTGATACAGT[A/G]TCAAACGTTAGCCCC | 23947 |
rs223624753 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140754479 | GCCCTTAGCTGAATG[A/G]GAATTCCAACAGGTC | 23947 |
rs223671284 | in-del | -/CG | | | intron-variant | Mid2 | Mm_Celera | X:140692942 | CATGCCTCCTCCCGT[-/CG]AGAAAGAGAGAGAGA | 23947 |
rs223671297 | in-del | -/T | | | intron-variant | Mid2 | Mm_Celera | X:140720454 | ACTTTTGTGTATTAA[-/T]TTTTTTTCTCTCCAC | 23947 |
rs223703968 | in-del | -/TATGTATGTATG | | | intron-variant | Mid2 | Mm_Celera | X:140732032 | ATACATACACACATA[-/TATGTATGTATG]TATGTATGTATGTAT | 23947 |
rs223838670 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140701626 | ATTCTTTCCATTGGC[G/T]ATTGAGTAAACTTGT | 23947 |
rs223847259 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140720670 | ACTGTAAATACACAA[C/T]AAGTTACAATAAGAC | 23947 |
rs223870206 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140721756 | TGTGGGTCGCAATAT[A/G]ATTATCCTTTGCTTT | 23947 |
rs223916669 | snp | A/G | | | intron-variant | Mid2 | GRCm38.p3 | X:140717073 | CCATATACCTCTTGG[A/G]TTGCTGTAAAGATAG | 23947 |
rs223962283 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140726565 | CTTTCTCTTGGCTCT[A/G]ACCCTCTTAACTGCC | 23947 |
rs223968849 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140725614 | TGTCAGAGATTGATG[C/T]TTGCACATAAGATGG | 23947 |
rs224024859 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140715368 | ACATGACTGTGTATG[C/T]GTGTGTCTCCCACTG | 23947 |
rs224092842 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140761528 | CTAAGAGATGTATAG[C/T]GTAGCTCGTGGCTTG | 23947 |
rs224129429 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140762317 | AAAGCAAACGTCTCC[C/T]GTTGCTGAGTTTTTC | 23947 |
rs224159150 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140757929 | ACTCTCTTCTAGTCT[C/T]TGTGGGTACTCCATA | 23947 |
rs224213781 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140684440 | CAAGGTCAATCTTGG[C/G]TCATAGTGGGTTTGC | 23947 |
rs224227070 | in-del | -/GAGCATCTGA | | | intron-variant | Mid2 | Mm_Celera | X:140730518 | AAAGACTTGGAGAAT[-/GAGCATCTGA]GAGATTTCCCCTTAA | 23947 |
rs224245707 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140679606 | AGATGTAGCCAACTA[C/T]TGGTTTCCTATTGCT | 23947 |
rs224308130 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140680578 | TGAGACTTTCTTCCA[C/G]TAAGTGATGTGGTAA | 23947 |
rs224345316 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140688179 | CTCAAAAAGGCCAAG[C/G]CTATACAACACAAAT | 23947 |
rs224370011 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140675796 | TCTGTGCCTCATTTT[C/T]CTAAGTCTGTGATGG | 23947 |
rs224375164 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140761003 | CAACTCTTTAAGTGC[A/G]TGGAAAATAGTCATT | 23947 |
rs224403372 | in-del | -/G | | | intron-variant | Mid2 | Mm_Celera | X:140701856 | TCCCAGGAAGGACTT[-/G]GGGCTACCAATACAT | 23947 |
rs224421839 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140691379 | TAGTGCTGAAAAGGT[A/G]ATTGAGAGTTCCACA | 23947 |
rs224537710 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140708821 | AATTTATGAAATTCC[C/T]AGGCAAATGGATGGA | 23947 |
rs224586446 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140758751 | ATATTTGCTCAACCC[G/T]GCAAATATGTCTAAA | 23947 |
rs224622172 | snp | A/G/T | | | intron-variant | Mid2 | Mm_Celera | X:140674219 | TGTTGTCTAATCTAA[A/G/T]GCATGTCAGATTTAC | 23947 |
rs224633289 | in-del | -/AAGT | | | intron-variant | Mid2 | Mm_Celera | X:140729457 | TTTCTAAAGAAAGTA[-/AAGT]AAGTATCTAAGTATT | 23947 |
rs224636727 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140714673 | TGACGGCTTTTGAAG[C/T]GAAAGGATGAGCACG | 23947 |
rs224665487 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140711762 | AAATGTATTCAGAAG[C/T]GAAACAATCCTATAG | 23947 |
rs224733304 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140673422 | CCCTCTTTTAGACCT[C/T]GGCTACTATTATGCT | 23947 |
rs224758257 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140723916 | ACCTCCTTTTAAAAA[G/T]TAGATTTAGGTATTT | 23947 |
rs224771016 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140714060 | TGAAACTTACAATGC[C/T]CTGCAAATGAATGAA | 23947 |
rs224782457 | snp | A/G | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140677617 | ATCACAGTCTCAGAG[A/G]AGAGATGCCAGTGGA | 23947 |
rs224811498 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140719904 | TCCTGAAGGCAGGAG[C/T]CATGGCTTTGCCATA | 23947 |
rs224830684 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140754664 | GTTTCTCTGTATAGC[C/T]CTGGCTGTCCTGGAA | 23947 |
rs224857357 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140671543 | TAAATAGAAAGGACT[C/G]TATAATAATAGGATA | 23947 |
rs224872319 | snp | A/G | | | intron-variant | Mid2 | GRCm38.p3 | X:140718367 | ATCAAGAGCTACAGA[A/G]GGAAGAGTAAGGGAA | 23947 |
rs224872726 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140711034 | AAATATATTTTTATG[A/G]TAGGGCTTTTTATCA | 23947 |
rs224892705 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140723351 | AACAATGGCCCCACC[A/G]TTAAGGAGCTTGCAT | 23947 |
rs224935247 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140762298 | TGTGCACTCCGATTT[C/T]AAGAAAGCAAACGTC | 23947 |
rs225002028 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140712583 | ATAGTTACCTATGGC[A/C]ATTTTATTCCAAAAG | 23947 |
rs225059501 | in-del | -/T | | | intron-variant | Mid2 | Mm_Celera | X:140705948 | TAATGTGTGTGTGTG[-/T]GGGGGGGGGCAGAAG | 23947 |
rs225070231 | in-del | -/GTGT | | | intron-variant | Mid2 | Mm_Celera | X:140736774 | ATGCTGGTTATGTAC[-/GTGT]GTGTGTGTGTGTGTG | 23947 |
rs225099974 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140750024 | AAAAAATCAAATTTA[C/T]TTCTTATAATGCATC | 23947 |
rs225179021 | in-del | -/ACAC | | | intron-variant | Mid2 | Mm_Celera | X:140733657 | ATATTGTATTTAGGA[-/ACAC]ACACACACACACACA | 23947 |
rs225182797 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140722720 | ATTTTAAAATATGTG[C/G]TCTCCTAAAACCTAT | 23947 |
rs225216511 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140668087 | TCATTCGGTCTTTAT[A/T]CAGCTTGCTAAATTT | 23947 |
rs225230434 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140718487 | TCAGATGATAAAATG[A/G]TACTTGCTTCTTTCT | 23947 |
rs225267290 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140748395 | CCTATTAATCATTAG[A/C]TCATAAGAATTGCTG | 23947 |
rs225267412 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140758123 | GTGAGCAGCTTTTCT[C/T]GAGCAACAGCACTCA | 23947 |
rs225322744 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140713495 | CTATCACATACTTGC[A/G]GCTCTAGGTTTTCTC | 23947 |
rs225329912 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140755194 | CAAAGAACACTCTTC[A/C]CTTTTTCATATATAT | 23947 |
rs225354045 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140757523 | GTTACATGACCTCCT[A/G]AGGATACCAGAATCT | 23947 |
rs225359327 | in-del | -/CA | | | intron-variant | Mid2 | Mm_Celera | X:140744265 | AGTCTCCTCTCTCCC[-/CA]CACAGCTTTCCTTAC | 23947 |
rs225368852 | in-del | -/TT | | | intron-variant | Mid2 | Mm_Celera | X:140714375 | AGTAAAAATGAAAGC[-/TT]TTTTTTTTCACTATA | 23947 |
rs225390730 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140723854 | TTCTCATGATCACTA[C/T]TGGAATTAAGTCATT | 23947 |
rs225401432 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140721682 | TATTCTGTTTCCCTG[A/T]CCCAGGGAGATCCAT | 23947 |
rs225406000 | in-del | -/CCC | | | intron-variant | Mid2 | Mm_Celera | X:140721547 | ACTCGGTTTCTATGT[-/CCC]CCCCCCATATGCCCT | 23947 |
rs225449848 | in-del | -/T | | | intron-variant | Mid2 | Mm_Celera | X:140738930 | CCCTCTCTCTCTCTC[-/T]TTCTCTCTCTCTCTC | 23947 |
rs225457057 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140703093 | CAGCTGCATGGTATG[C/T]TTAGCCAGGATTGAG | 23947 |
rs225525871 | snp | A/G | | | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140734654 | TTTCTTATCTGCTGA[A/G]TGGAAACAATGATAC | 23947 |
rs225550238 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140723168 | TTAAATCCACAGGTA[C/T]GGAACTTACAGATGT | 23947 |
rs225559542 | in-del | -/G | | | intron-variant | Mid2 | Mm_Celera | X:140718670 | AATCTTCTGAGATTA[-/G]GTATTTCTATTATCC | 23947 |
rs225562739 | in-del | -/TGTG | | | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140735176 | AGTGGTTAAGAGCAC[-/TGTG]TGTGTGCACTTGCAG | 23947 |
rs225579935 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140668825 | AGAAAGTTTTCTGTG[C/G]ACTGTAGAAGGCTGT | 23947 |
rs225602650 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140728777 | AACTGGGGTCCTCAT[C/T]CTTGCATGGCAGGCA | 23947 |
rs225613000 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140695463 | CCTTCTAAAATGTAA[A/G]TTGAAATGCCGCCGT | 23947 |
rs225614365 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140682067 | TGAATTCAAACAATA[C/T]TCATGGTTCTTACTT | 23947 |
rs225652707 | in-del | -/CAAT | | | intron-variant | Mid2 | Mm_Celera | X:140758140 | AGCAACAGCACTCAC[-/CAAT]ACACACACACATACA | 23947 |
rs225689706 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140705696 | TACATGTATTATTTC[A/G]TTTAATCCTCTCAAA | 23947 |
rs225727257 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140702022 | TAGATGGAGAAGCTA[A/G]ATCTATTGTGCAGTC | 23947 |
rs225786003 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140758257 | AATGCATTTTTATTG[C/G]AGTAAATAATAAGAG | 23947 |
rs225797180 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140721614 | TCCATATCTCTTCCA[A/G]TTTGATCCTTCCTCT | 23947 |
rs225827864 | snp | C/T | | | synonymous-codon | Mid2 | Mm_Celera | X:140761249 | GAACCATTACACAGT[C/T]CATGGACTCCAGAGT | 23947 |
rs225849684 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140758815 | TATATAGTTGCATGG[A/T]AGAGTACTTAAACAG | 23947 |
rs225928584 | in-del | -/TCCTC | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140677413 | TCTGTCTTTTTTTTT[-/TCCTC]TCTCTCTCTCCATGC | 23947 |
rs225934811 | in-del | -/A | | | intron-variant | Mid2 | Mm_Celera | X:140743498 | CAGATTTTTTTTTTT[-/A]TTAAATAAGATGTCA | 23947 |
rs225963131 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140732002 | AAAATATATTTACGA[A/T]GGCATAACTACATAC | 23947 |
rs225967610 | in-del | -/TTTTTTCTTT | | | intron-variant | Mid2 | Mm_Celera | X:140675111 | TATCTATCCTTTCTG[-/TTTTTTCTTT]TTTTTTCTTTATGTT | 23947 |
rs226045732 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140739714 | TCACCCTGACAAAAT[C/T]CTATACCTGAGTCAG | 23947 |
rs226054988 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140725238 | AACATAGCCCATGGA[C/T]AGGCAACAGCTTTTG | 23947 |
rs226067668 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140725699 | CCCATTCCTGCATTT[C/G]TTGTAGACGGGATAA | 23947 |
rs226134292 | snp | A/C | | | upstream-variant-2KB | Mid2 | Mm_Celera | X:140663877 | GGAGCTAGAAAGAAT[A/C]TCCTCTGAGGTGGCT | 23947 |
rs226176210 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140728053 | GTGATCTGGCTTAAC[A/C]CCTTAGCTTTGATGC | 23947 |
rs226207420 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140685021 | GTCTTTTAGTCACTA[G/T]TGGCTGAGCTAAATA | 23947 |
rs226207550 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140699992 | GATAACATTCAAAAT[A/G]TAAATAAAGAAAATA | 23947 |
rs226228590 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140689356 | GGTTCAGGGCCATAA[A/G]TGAGGAACACACAGC | 23947 |
rs226245384 | in-del | -/C | | | intron-variant | Mid2 | Mm_Celera | X:140683512 | CTCATTCTGTCACTG[-/C]TTTTCCCCAGTCAAT | 23947 |
rs226277060 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140685990 | ACTTCCTTATTGGGG[A/T]ATTGGGGCAAAGTCA | 23947 |
rs226394135 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140696764 | ATTCAGAAGTTAACC[C/T]GTGCCTTAAGGATGT | 23947 |
rs226402962 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140720342 | CCCAGGAAAGCCATG[A/G]CCCATGTTCCATCCA | 23947 |
rs226480583 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140680237 | ATTAGTGTTGGTAAG[G/T]GTAGCAGCAGTCAGA | 23947 |
rs226574788 | in-del | -/TGTGTGTGTGTA | | | intron-variant | Mid2 | Mm_Celera | X:140669380 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTA]TGTGTATACAGTCCA | 23947 |
rs226588002 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140692087 | CAGCTCTCAACGCTA[A/G]CATTTGGTGATAAGG | 23947 |
rs226606107 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140718709 | GTAGAGGAAACTGAG[C/T]CCACTTGTTGTAAAG | 23947 |
rs226635920 | in-del | -/GTGCGTGC | | | intron-variant | Mid2 | Mm_Celera | X:140687194 | TGTGTGTGTGTGTGT[-/GTGCGTGC]GTGTGTGTGTGTATT | 23947 |
rs226734861 | snp | A/G | | | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140734277 | GAAAAGGTAAAGAAG[A/G]GATGATTGCAGAGTT | 23947 |
rs226742531 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140695293 | TCATATGTGAAACTG[A/G]AAAATAGGATGGTGT | 23947 |
rs226769523 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140681388 | GTGAGTAAGAGAGAG[A/G]GGTGAGGGAGGAAGG | 23947 |
rs226779073 | in-del | -/TT | | | intron-variant | Mid2 | GRCm38.p3 | X:140710181 | CTCCCTCCCTCCTTC[-/TT]CCTCCCTCTCTTCTT | 23947 |
rs226822142 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140737028 | TCGTTACTCTTAACA[A/G]CTGAACTCTGTCTCT | 23947 |
rs226824439 | snp | A/C/T | | | intron-variant | Mid2 | Mm_Celera | X:140757128 | CTTCTTCCAGCAAGA[A/C/T]TATACCTCCTAAACC | 23947 |
rs226830532 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140738278 | TTTTTAATTAAGCGC[A/G]GTATGTTTTATGTCA | 23947 |
rs226868747 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140727391 | TAGGTTAACCAAAGC[A/C]GCTAAAATCCACGAG | 23947 |
rs226948477 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140690886 | CAGAATTAAAGAAAG[A/G]CGAGAAAGACACCTC | 23947 |
rs226954484 | snp | C/T | | | upstream-variant-2KB | Mid2 | Mm_Celera | X:140662541 | AGTGGGTGTTCCAAG[C/T]GGGTCCTTTGGGAAT | 23947 |
rs226963696 | in-del | -/GAACATCCCA | | | intron-variant | Mid2 | Mm_Celera | X:140666240 | TCTCTGTCAACCTGT[-/GAACATCCCA]GCAATGCGGCTTCTT | 23947 |
rs226998984 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140695926 | ATGTTAGAATCTCTC[A/T]AAAATCGCCTTTTCT | 23947 |
rs226999090 | snp | A/G | | | intron-variant | Mid2 | GRCm38.p3 | X:140708042 | TCCTCCACTGTTGGT[A/G]GAATTGCAAGCTGGT | 23947 |
rs227022032 | in-del | -/A | | | intron-variant | Mid2 | Mm_Celera | X:140717576 | TGTATATGTATATAT[-/A]ATGGCTTTTCACAGC | 23947 |
rs227060366 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140696695 | TATACATCATAGCAA[C/G]AAGCAACAACATAGC | 23947 |
rs227085845 | in-del | -/AAACAAACAAAC | | | intron-variant | Mid2 | Mm_Celera | X:140742567 | AAACCCTGTCTTGAA[-/AAACAAACAAAC]AAACAAACAAACAAA | 23947 |
rs227132844 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140736369 | TAGCTGTCAGTCCGA[A/T]CCTTTTAGAGCCAGC | 23947 |
rs227156686 | snp | C/T | | | utr-variant-3-prime | Mid2 | Mm_Celera | X:140764537 | CTTTCCTCCCTCTTG[C/T]CTCATGTACAAACAC | 23947 |
rs227164183 | in-del | -/CA | | | intron-variant | Mid2 | Mm_Celera | X:140720989 | TACCACAATTCTGCC[-/CA]TCCCCATCTTCTGTG | 23947 |
rs227169858 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140707502 | CTTGTCAAAGATCAA[A/G]TGACCATATGTATGT | 23947 |
rs227206943 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140723552 | CCTGGCAAACATTTT[A/T]AAAACATATTCTTAT | 23947 |
rs227272395 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140667388 | TTCAAAGCACCTTTA[A/G]TGTACAGAAGCCTCT | 23947 |
rs227282035 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140696335 | AGTAATGCCAAGATA[C/T]ACAACTATAATATAT | 23947 |
rs227356770 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140754691 | GGAATTCATTCTGTA[G/T]ACCAGGCTGGCCTAG | 23947 |
rs227370703 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140741894 | TTCAGGACATTACAG[A/G]CTCTTGCTGTTACTT | 23947 |
rs227405814 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140701049 | ACCGGAACCTTGAAA[A/G]GTAGGATAATTTGGG | 23947 |
rs227431234 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140744029 | ATGTGTCCCCATTGA[C/T]CACTTTTACTTGCAG | 23947 |
rs227443122 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140724350 | TATGGTTGGGAGGGC[A/G]TTCTGTTATATGAAT | 23947 |
rs227467159 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140702191 | ACATGTTAAGTGTTG[C/T]ATTGGGAATATTTTG | 23947 |
rs227582494 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140709326 | TGCATCCCCATAAGA[A/G]GAACAACAGTATCAA | 23947 |
rs227582555 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140700454 | GCAGCTGGCTGGCTG[A/C]GTCTGGATGTCAGGA | 23947 |
rs227594045 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140710087 | CTTTCCAAGGCGACC[G/T]AACTGATTAGGTGAG | 23947 |
rs227652696 | in-del | -/CAGGCTTA | | | intron-variant | Mid2 | Mm_Celera | X:140669794 | TCTTCATTTGTTCCT[-/CAGGCTTA]CAGCTCTGCCAGTGT | 23947 |
rs227673139 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140751592 | ATAATCCCAACATGC[A/G]GGAAGTTGAGGCAAT | 23947 |
rs227674573 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140740093 | TTTTTAAGTGGATAC[C/T]ATTCTGACTTGGATA | 23947 |
rs227701085 | in-del | -/A | | | upstream-variant-2KB | Mid2 | Mm_Celera | X:140662865 | AGACTGAAAACTCTG[-/A]AAATCATAATCCAAA | 23947 |
rs227748716 | in-del | -/GAAAA | | | intron-variant | Mid2 | Mm_Celera | X:140759412 | GTGATAAAGGTTTTC[-/GAAAA]CCGTGATTTATTGCC | 23947 |
rs227774922 | in-del | -/TTTT | | | intron-variant | Mid2 | Mm_Celera | X:140666593 | CCCAGCATCCCCACC[-/TTTT]TTTTTTTAACCTCCT | 23947 |
rs227811343 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140742485 | GAGGCAGAGGCAGGT[C/T]GATTTCTGAGTTTGA | 23947 |
rs227814384 | snp | A/T | | | utr-variant-5-prime, intron-variant | Mid2 | GRCm38.p3 | X:140664756 | CTCCAGAGGAGGGGC[A/T]CGGGGAGTTGGGAGT | 23947 |
rs227891942 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140729324 | GCAGTTTACTCACCA[A/G]ACTAGACTGTCTCCC | 23947 |
rs227902452 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140666318 | TGCTGAATGGCATTA[C/G]TTGTGTGTCTGTCTC | 23947 |
rs227903378 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140743838 | AGCAAAGATGAAATA[C/T]ATATTTAAACCACTA | 23947 |
rs227906023 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140730918 | AGTAGTTAATACAAC[A/C]TCTCTGAAAGGAGCT | 23947 |
rs227910175 | in-del | -/G | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140677754 | GAAAACAAAACAAAA[-/G]TAAAACAAAACAAAA | 23947 |
rs227924178 | in-del | -/G | | | intron-variant | Mid2 | Mm_Celera | X:140691445 | AGACCTCAAATACTA[-/G]CTCCTAGTGACAAAC | 23947 |
rs228008726 | in-del | -/AA | | | intron-variant | Mid2 | Mm_Celera | X:140684147 | ACTTAAATAAAAATG[-/AA]AAAAAAAAGTTGGGA | 23947 |
rs228028049 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140753228 | GACCTTGAACTTCTG[A/G]GTCTTCTGTCACCAC | 23947 |
rs228043562 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140753910 | GCCGAGGATGGCCGA[A/G]CACCAGCACTGACAG | 23947 |
rs228052074 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140758973 | CTGCTATGTAATTTT[A/T]AAATGTGAAATTATA | 23947 |
rs228112400 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140701267 | GGGTACCACATTTAT[C/T]GCCAGAGATTTCACT | 23947 |
rs228139811 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140752153 | AAAAAAAACCACTTG[C/T]CTCTTGCAGCTCCAT | 23947 |
rs228139857 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140759921 | CATACCTTGAATTAA[G/T]TATGAATCACTTGAT | 23947 |
rs228208918 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140708710 | CTATTGCCAGGAAAC[C/T]GTGGGGTGGAGCTTA | 23947 |
rs228212937 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140692511 | ATAAATTCCTACACC[C/T]GTCTACAAAGTTATG | 23947 |
rs228218449 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140703632 | TATTTGGGGACCATG[A/C]AAGTACATAAAAATA | 23947 |
rs228261719 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140706713 | GCACGGGGGCGGGGG[C/T]GGGCGCAGATCAGAA | 23947 |
rs228290425 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140667155 | ATATATACAATTAGG[C/T]ATAGAAAGTAATGGT | 23947 |
rs228311359 | in-del | -/C | | | intron-variant | Mid2 | Mm_Celera | X:140679624 | GTTTCCTATTGCTTT[-/C]CCGATATGTGGTATA | 23947 |
rs228332167 | in-del | -/CCA | | | intron-variant | Mid2 | Mm_Celera | X:140682504 | TTAAATCCCTTGAGG[-/CCA]GATACAATGGTTTTT | 23947 |
rs228344283 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140675275 | TGACCTTATATAAGG[C/T]CATTGTGACCTAGAG | 23947 |
rs228363860 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140707839 | GAGTGAGTTTCAAGA[C/T]CGCCAGGGCTCCACA | 23947 |
rs228393959 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140708159 | TATACCTAGAAGATG[C/T]TCCAACATGTAATAG | 23947 |
rs228474409 | in-del | -/C | | | intron-variant | Mid2 | Mm_Celera | X:140741513 | GCTCCTCAGCTGGGG[-/C]TGGGACTTCATGCCC | 23947 |
rs228509060 | in-del | -/A | | | intron-variant | Mid2 | Mm_Celera | X:140710884 | GTTACAAAACAAACC[-/A]AGAAAAAACAAAGCA | 23947 |
rs228542584 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140705232 | AATACTTAACCCAGG[C/T]TAGTCTTAGCTCACA | 23947 |
rs228570930 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140711158 | TGCATGTGTGTATAT[A/G]TGTGTGTGTGTGTGT | 23947 |
rs228642520 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140718975 | TGTAGTGTAATATAT[A/G]TGGACAGACACCAAT | 23947 |
rs228670250 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140746604 | CAAGGTGTTTCAAAG[A/G]GAACACCACTCCTCT | 23947 |
rs228704636 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140710368 | ACCGCACCCGGTTTA[G/T]GTGGTGGTACGGATA | 23947 |
rs228729666 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140718039 | GTTAATTATGGGGTA[C/T]CCTAGAGCAGAAAAA | 23947 |
rs228735776 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140732632 | ACATTTGATGGAGAG[A/G]TGGTTCAGTGGTTAG | 23947 |
rs228745711 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140711320 | TTTTCTTACTATACT[G/T]ATAATTTTGGATCTA | 23947 |
rs228746592 | snp | A/G | | | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140734847 | GAAATCTAATGGATT[A/G]TGTCTATGTTTCCAG | 23947 |
rs228758148 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140665961 | CATAGGACACACTGC[A/G]ACTGAAGCAGGGACA | 23947 |
rs228758520 | in-del | -/TG | | | intron-variant | Mid2 | Mm_Celera | X:140697309 | GGACAGGATGGCTTA[-/TG]TGGCAGTCCATGGCT | 23947 |
rs228770554 | in-del | -/T | | | intron-variant | Mid2 | Mm_Celera | X:140672851 | GCAACAATTTCAATA[-/T]TTTTAAGTAAATAAG | 23947 |
rs228772359 | in-del | -/TATAAC | | | intron-variant | Mid2 | Mm_Celera | X:140692204 | TGTTAAAGTTATACA[-/TATAAC]TATACTAGTAAAACT | 23947 |
rs228860668 | in-del | -/TT | | | intron-variant | Mid2 | Mm_Celera | X:140762459 | AAACATTCTTTTACA[-/TT]TTTTTTTTCAGGCCA | 23947 |
rs228882843 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | Mid2 | Mm_Celera | X:140664490 | CGCTTCACACACACC[A/C]CCCGGTCGTGGACGC | 23947 |
rs228926699 | in-del | -/TT | | | intron-variant | Mid2 | Mm_Celera | X:140722758 | TTAGACATTTCTCCG[-/TT]TTTTTTCATATTTCA | 23947 |
rs228972023 | in-del | -/GT | | | intron-variant | Mid2 | GRCm38.p3 | X:140669348 | ACTTAGGAGAGCAAA[-/GT]GTGTGTGTGTGTGTG | 23947 |
rs229007279 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140738816 | CTATGCATGGTTTTA[C/T]TTTTTTGAAATCAAT | 23947 |
rs229021972 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140745195 | TTGCAGATCCCTTTA[C/G]TTCCTTGGGTACTTT | 23947 |
rs229064184 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140668424 | CTTGTGGAAATCTAC[A/T]CTTTTCTTCCACTGC | 23947 |
rs229115388 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140736899 | TTTGCCTGGATGTAT[A/G]TCTGTGCACCATGTG | 23947 |
rs229121178 | snp | A/G | | | intron-variant | Mid2 | GRCm38.p3 | X:140717502 | tatatgtgtgaatgt[A/G]tatatgtatatgtat | 23947 |
rs229142973 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140667544 | GGAGTAGGGAGAGAG[A/G]GTTATGGCACATGAA | 23947 |
rs229144756 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140755374 | CCCAGAACACTTGGT[C/T]GCCATCTTCTGGCTC | 23947 |
rs229144804 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140744222 | TATTTCCTTAATAAT[A/G]CTGTTCTTCCTTATT | 23947 |
rs229222615 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140754767 | AGGCGTGCGCCACCA[C/T]GCCCGGCTCAATTTA | 23947 |
rs229223675 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140747381 | TGTCTTTGCTCCCAT[C/G]TTTCTGTTAGATGAC | 23947 |
rs229223746 | in-del | -/TTTG | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140677067 | GACGAGGTTTTTTTT[-/TTTG]TTGTTTGTTTGTTTT | 23947 |
rs229277584 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140693997 | AGACATTACCCTATA[A/C]TGGGGCATAGAACCT | 23947 |
rs229283302 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140669917 | CATTTTTAAATAATA[C/T]TTTTATTCTGTGAAA | 23947 |
rs229296758 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140671737 | CTAATACCCTGAAAG[A/G]TTAAAGCTAATATCC | 23947 |
rs229297391 | in-del | -/TT | | | intron-variant | Mid2 | Mm_Celera | X:140721841 | CCTCACTCGGGATGA[-/TT]TTTTTTTTCTAGTTG | 23947 |
rs229330037 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140747475 | TCATTGAACACGTGC[A/G]TCACAGCAAACTTGT | 23947 |
rs229365190 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140725865 | TAATTGTGTACATAC[A/G]TAAAACACTAGATGC | 23947 |
rs229474466 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140739837 | AGTGCAAAGTACTGA[C/T]TAGAGTAAGTTGGTT | 23947 |
rs229546905 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140712119 | CTCTAGTAAATATGT[C/T]AGTATTTATCCAGTA | 23947 |
rs229601973 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140713167 | TTTCTGAATTTGGAC[A/C]TTGCCATTGCTCAGC | 23947 |
rs229628489 | in-del | -/ACGGGCAGTC | | | intron-variant | Mid2 | Mm_Celera | X:140753040 | CATGAGATTTGTCTT[-/ACGGGCAGTC]TTCTGTTGGTCAAAG | 23947 |
rs229657682 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140707331 | AAGCTGGCAGAAGAC[C/T]GTATTTCTAGAAGTA | 23947 |
rs229704305 | snp | C/G | | | intron-variant | Mid2 | Mm_Celera | X:140728755 | TTATGCATGTTCTAG[C/G]GATCCAAACTGGGGT | 23947 |
rs229729604 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140668628 | GGTAACAGAGGAGGC[A/T]AGAAAAGTGCTTCTC | 23947 |
rs229731295 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140695744 | ATTGGATAAGGGGAC[A/G]CTCAGCTTAGAATTT | 23947 |
rs229758409 | in-del | -/ACACACACACAC | | | intron-variant | Mid2 | GRCm38.p3 | X:140681308 | AAAGGAAAAGGGAGT[-/ACACACACACAC]ACACACACACACACA | 23947 |
rs229766879 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140718363 | TGGGATCAAGAGCTA[A/C]AGAAGGAAGAGTAAG | 23947 |
rs229769787 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140729993 | TAGATGCTTCCTGGT[A/G]TGTTCTCATAGGGCT | 23947 |
rs229814547 | snp | A/G | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140676508 | AGTTTAGTACATTGA[A/G]TGGATTTGATTTAGA | 23947 |
rs229838641 | in-del | -/T | | | intron-variant | Mid2 | Mm_Celera | X:140761958 | AAAACGTTGGCAATC[-/T]TTTTAATCAACGAAA | 23947 |
rs229840393 | snp | A/C | | | intron-variant | Mid2 | Mm_Celera | X:140755407 | ACATTATTCCTGCTT[A/C]CTCTTTTCCAGTGTC | 23947 |
rs229849818 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140760416 | ACAACAAACAAAAAA[G/T]AAATAAAAACAAAAC | 23947 |
rs229955990 | snp | A/G | | | intron-variant | Mid2 | Mm_Celera | X:140687061 | GCGAGTGGTAGCACC[A/G]ACTGACATATTTGCT | 23947 |
rs230010427 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140675531 | TGAAAGGGGTTGTAA[C/T]AGAAGTACAGTGTCA | 23947 |
rs230010482 | snp | G/T | | | intron-variant | Mid2 | Mm_Celera | X:140687903 | TCTGTGCCAGAAGAG[G/T]AACCTCTCTTCCTTT | 23947 |
rs230026684 | snp | C/T | | | upstream-variant-2KB, intron-variant | Mid2 | Mm_Celera | X:140677411 | TGTCTGTCTTTTTTT[C/T]TTCCTCTCTCTCTCT | 23947 |
rs230035478 | snp | C/T | | | intron-variant | Mid2 | GRCm38.p3 | X:140691307 | GCTGCCTTACAGTTT[C/T]AGATCTTTTAGTCCA | 23947 |
rs230049191 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140680278 | AATCTTGTCTGTAAT[A/T]TACTGCACACAGTAT | 23947 |
rs230063518 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140669313 | TAGGAACATAAAGTG[C/T]AGGCATGGAAGACAG | 23947 |
rs230081390 | snp | C/T | | | intron-variant | Mid2 | Mm_Celera | X:140678981 | TATATATCTTTGCTA[C/T]GATCTCCCCACCTCG | 23947 |
rs230101000 | snp | A/T | | | intron-variant | Mid2 | Mm_Celera | X:140689168 | TGTCAGCTCTAGAAC[A/T]GTGTTGTTAAAATGG | 23947 |