SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6172242 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Kbtbd12 | Mm_Celera | 6:88620516 | GAATTGTGCCCAGGG[A/T]ATCACAGGTGCTGTT | 74589 |
rs6174943 | snp | C/T | 0.5 | 0 | intron-variant | Kbtbd12 | Mm_Celera | 6:88620926 | GTTCAAGTTAAATAA[C/T]TAATGGATCTATGTT | 74589 |
rs13478880 | snp | G/T | 0.447971 | 0.152668 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88587087 | TCTGGCCTTGACTTG[G/T]TTTTGCTGCCTATTT | 74589 |
rs29869230 | snp | C/T | 0.5 | 0 | intron-variant | Kbtbd12 | Mm_Celera | 6:88623979 | CTAGAATACATGCTG[C/T]ATTCATAATGTGTTT | 74589 |
rs29875293 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88589304 | TCAATAAGTCAGCGC[C/T]GTGGCTTTCATTTAT | 74589 |
rs29876985 | snp | C/G | 0.5 | 0 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88577537 | ATTGGATGTGGGTGG[C/G]TGGGAGGGATGTAGG | 74589 |
rs29882095 | snp | G/T | 0.5 | 0 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88577219 | TAGGCATCTAGCTTT[G/T]GGTAATGTGTGTTAG | 74589 |
rs29921386 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88575760 | ACGCTGGGTGTGCAG[A/G]AGTGTATCGGCCTCT | 74589 |
rs29930955 | snp | A/G | 0.5 | 0 | synonymous-codon | Kbtbd12 | GRCm38.p3 | 6:88586904 | CCAGAAGTCCCCATC[A/G]GGGTTGTAGATCTCC | 74589 |
rs29937498 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88584369 | TTTTATAGCTTCCAC[C/T]GCCCCGCTCTCGATG | 74589 |
rs29967375 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Kbtbd12 | Mm_Celera | 6:88597592 | CCACCACCACCACCA[A/C]CAACAACAACAACAA | 74589 |
rs30015488 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88595212 | GTACAGTCACACAAG[C/T]CGCAGGAGAGGCAGA | 74589 |
rs30019951 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88578451 | CAGGAGCTGGGAATG[A/G]GGAGGATCTGATGCG | 74589 |
rs30022423 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88577344 | AATCAAGGCACAGTA[C/T]TGGTTATATATAAAT | 74589 |
rs30028285 | snp | A/T | 0.5 | 0 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88557393 | CTTTGATCATAAATT[A/T]AAAAAAAATAAAATT | 74589 |
rs30029715 | snp | A/T | 0.5 | 0 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88626087 | GTAAAGTGAGTAAAT[A/T]AAAAAAAAAAGAGTT | 74589 |
rs30033444 | snp | A/G | 0.5 | 0 | intron-variant | Kbtbd12 | Mm_Celera | 6:88586002 | AAAGAAAGAAAGAAG[A/G]AAAAAGAAAGAAAGA | 74589 |
rs30062610 | snp | C/G | 0.5 | 0 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88579026 | AATGGCGGAGCCTTT[C/G]GGGTCTGGGTTTTGA | 74589 |
rs30074031 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Kbtbd12 | Mm_Celera | 6:88590937 | GCCTTGGCTTCATAG[A/C]GCTTAGGTTGATGGT | 74589 |
rs30125273 | snp | C/T | 0.5 | 0 | intron-variant | Kbtbd12 | Mm_Celera | 6:88592249 | AGACCAAACTCCTAC[C/T]GATGCCTCTACAAAG | 74589 |
rs30168129 | snp | A/G | 0.5 | 0 | intron-variant | Kbtbd12 | Mm_Celera | 6:88585741 | TAATTCACAAAGAAA[A/G]CTGGGCAGTGGTGGC | 74589 |
rs30170054 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88577069 | CCATGTGACTCTTCC[C/T]TCTGCATACACTGCC | 74589 |
rs30209980 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88622910 | ATCTTTAGCTCTCAA[A/T]TTGACAATAGGTTGA | 74589 |
rs30215676 | snp | A/G | 0.5 | 0 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88580242 | TAACATGAGTCAACT[A/G]GGTGGTATTAGACAT | 74589 |
rs30218747 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kbtbd12 | Mm_Celera | 6:88596990 | TAAGAATAATAATAG[A/G]AATATCCCCAGCTCG | 74589 |
rs30222877 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88621345 | GGTGCAACACCCAAG[A/G]GTGTCTATAGCAATG | 74589 |
rs30225945 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88549643 | CATGTGTTCCTCCAC[A/G]CAGCCATGGTTGAGT | 74589 |
rs30316053 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88590155 | TGGCTATTTTCTTTC[A/G]TGTTTGAAAGCCACT | 74589 |
rs30316291 | snp | C/T | 0.5 | 0 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88566712 | TGCCTGCTCGTCGTG[C/T]GATCCAAAGCCACAG | 74589 |
rs30326843 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88612319 | CAATAGCCTGCTTTC[A/G]TGTGCTGTGTCTGAG | 74589 |
rs30349789 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88577572 | AAATATGTCAAGATG[A/T]ACGCTTCTTCCTGAT | 74589 |
rs30361465 | snp | C/T | 0.5 | 0 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88573653 | TAAACTTTAAATCAT[C/T]TTACTAAACTGACTA | 74589 |
rs30367067 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88595373 | TTATACATTCCGTGA[A/T]GTTGAAGTGGATTCT | 74589 |
rs30368579 | snp | A/G | 0.5 | 0 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88554919 | TGTGTGTGCGCGCGC[A/G]CGCACATGCGTGCAC | 74589 |
rs30410781 | snp | A/G | 0.5 | 0 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88622226 | TTTTAAAACCCGTTC[A/G]TAGCTCATAGACTGT | 74589 |
rs30414613 | snp | C/T | 0.5 | 0 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88586325 | ATTCAGTAATAAGCA[C/T]ACACACTAGGCATCA | 74589 |
rs30416337 | snp | G/T | 0.5 | 0 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88626042 | GAGGGAGGGGGGAAA[G/T]ATTGTGGGAGGGGTG | 74589 |
rs30417550 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88579677 | GCTATGGCAGGGAGA[A/G]AAGAGCAAATTAGAA | 74589 |
rs30426670 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Kbtbd12 | Mm_Celera | 6:88595791 | AAAAAAACCAACCAA[A/C]CAAACAAACAAACAA | 74589 |
rs30446467 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88617007 | CCCCATTTTTTTTCC[A/G]TCACAAAGAATTGTA | 74589 |
rs30455600 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88580154 | AAAAAACAGTGTTTG[C/T]TAAATAAGACATTAA | 74589 |
rs30481317 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88586529 | ATTTTTTTTTTTCTC[C/T]CCATACTCAACTACT | 74589 |
rs30509036 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88583416 | TGGAGGGAATGTTAC[A/T]GTGAAGTGGTAAACC | 74589 |
rs30513373 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88607100 | CCAGTTCCAGGGCTT[C/T]TGACATTCTGACACA | 74589 |
rs30517214 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kbtbd12 | Mm_Celera | 6:88580126 | GAAAACAAAGTTTAT[A/G]AAAGATAGATTTAAA | 74589 |
rs30550310 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88577009 | TTTCACAAAACAGAC[A/G]TAAGAGTGAGAATAA | 74589 |
rs30551005 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88589397 | TACCTTTATAGGTCA[C/T]ACCCAAATACACCCC | 74589 |
rs30557987 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88585587 | AGCACAGCCCGAGCA[C/T]GCACTACCCAGCTCT | 74589 |
rs30562256 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88584337 | TGGAAGGAGGAACTC[A/G]TGTTGTTTTTTTATG | 74589 |
rs30563215 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Kbtbd12 | Mm_Celera | 6:88566464 | ATTATATTATAATCT[A/C]AAAAAAATAAAAGAA | 74589 |
rs30617458 | snp | A/T | 0.5 | 0 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88576768 | AGGTGGAGAGCTTTT[A/T]AAGAAGCGGGGCTTT | 74589 |
rs30659900 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88628946 | ATATCAATATATAAA[C/T]TATAACTTACTATAG | 74589 |
rs30758242 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88608108 | GAAGATAGGGTTACT[A/G]TGCTTGCTCCATTTA | 74589 |
rs30765017 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | Kbtbd12 | GRCm38.p3 | 6:88628672 | TAAAGGCAGGGGAAT[A/C]AGGAATTTAAGGGGC | 74589 |
rs30802610 | snp | A/G | 0.5 | 0 | intron-variant | Kbtbd12 | Mm_Celera | 6:88585993 | GAAAGAAAGAAAGAA[A/G]GAAAGAAGGAAAAAG | 74589 |
rs30806233 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88625696 | AGTAAAGGACTTCAT[A/G]TTTTATTCACTTCTC | 74589 |
rs30812446 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kbtbd12 | Mm_Celera | 6:88566497 | TTTAAAAGTTAGCGC[A/G]CTTGGGATAGCATTG | 74589 |
rs30850149 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88593139 | GGAAGACTGGAGTAA[A/G]AAAACATGAATTAGG | 74589 |
rs30860670 | snp | C/G | 0.475309 | 0.108333 | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88629131 | TGGTTCTCTTCCTCT[C/G]CTACTTCAGTTTGCC | 74589 |
rs30869683 | snp | C/T | 0.5 | 0 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88583590 | CCCCCGCAAATTTAA[C/T]AGTAACATACAAATA | 74589 |
rs30894814 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Kbtbd12 | Mm_Celera | 6:88597595 | CCACCACCACCAACA[A/C]CAACAACAACAACAA | 74589 |
rs30899872 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88577570 | GGAAATATGTCAAGA[C/T]GAACGCTTCTTCCTG | 74589 |
rs30916155 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88584551 | TGCTACTCCTCAGCT[C/T]GGTGCACAGCAGCTG | 74589 |
rs30957170 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Kbtbd12 | Mm_Celera | 6:88588425 | ACGCAGGATGTGCTT[A/G]GCTGCCTTCTCTCCT | 74589 |
rs30987811 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88577835 | AAAAAGTATTCCACC[C/T]AAATTCTGCTGAAGC | 74589 |
rs31001079 | snp | C/T | 0.5 | 0 | intron-variant | Kbtbd12 | Mm_Celera | 6:88577696 | GGATCTGGTCAGAGA[C/T]AATCATCTTGGCCGT | 74589 |
rs36242543 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88556210 | GAATTCAGATTTTAC[C/T]GCAGAAGGACAAACA | 74589 |
rs36243669 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88619216 | CTCAGAGTGAAGGAA[A/G]AAAGAAGTAAAAAGA | 74589 |
rs36266630 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612170 | ACTTCAAGCTAAGGA[C/T]TGAGGTGTCTCTTGT | 74589 |
rs36268429 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88594551 | CAGTCTCACAATGTC[G/T]GTGTTTCCAAAGTTC | 74589 |
rs36270386 | snp | C/T | 0.336735 | 0.234472 | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88628039 | CATTTAGAAGCAACT[C/T]ATTGTTTTGAAACCA | 74589 |
rs36272215 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88602571 | TCTGTTGCTATGAAG[G/T]TCCATGCCACTGTGG | 74589 |
rs36272237 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Kbtbd12 | Mm_Celera | 6:88550586 | ATCTGTGAACTCAAT[C/T]AACCCTGGATGTAAA | 74589 |
rs36277692 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88554526 | GGAGGAAGCTGTTCA[C/T]TTCATGGCAGCTGGG | 74589 |
rs36283645 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Kbtbd12 | Mm_Celera | 6:88608476 | TTTCACAATGATAAA[C/G]TATTTATTAGACCAG | 74589 |
rs36283901 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88563228 | TTGCCACTTTAAGTG[A/G]AGTATAAGAATCTTT | 74589 |
rs36290052 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88560289 | TGTGATGAAAGGGCA[G/T]GTACCACAAAGTCCA | 74589 |
rs36297888 | snp | A/C | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88563699 | TTTGATATCTGTCCT[A/C]TCACACATTATCTGT | 74589 |
rs36299791 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88557728 | GAGGCGTGGCCAACC[A/G]ACAGCAGCCCTGCAC | 74589 |
rs36322967 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88587086 | TTCTGGCCTTGACTT[C/G]TTTTTGCTGCCTATT | 74589 |
rs36337492 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88579199 | TATGGAAGATACCAG[A/G]GCAGCAAACCCTTAG | 74589 |
rs36340203 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88556851 | AGTTGAAAACTGTTT[C/G]TGAGAGTTTCTCTGG | 74589 |
rs36366497 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88611595 | CCCTGAGACTTGGGG[C/T]TGTAAGTACTCTGTC | 74589 |
rs36370673 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88555895 | ATTAGCTGTTGAGAT[A/C]ATGACCTGGTCCTTT | 74589 |
rs36387376 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88608177 | AGTAGATTTTGTCTA[C/T]CATCAATACAGCTAA | 74589 |
rs36390603 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88587310 | TCTTCCGTGACTCAT[C/T]ATGGCAGGCTGGCTT | 74589 |
rs36392144 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88564149 | GTTTCATCCTTAGGG[C/T]CTGCATGGTTAAGGA | 74589 |
rs36392632 | snp | G/T | 0.375 | 0.216506 | synonymous-codon | Kbtbd12 | Mm_Celera | 6:88547911 | GGAGATAACCTCATG[G/T]CGATCTGAAAGACAG | 74589 |
rs36398320 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88578732 | TTAGGAGAGGCCCAG[A/T]GTGGGACATCAGGCA | 74589 |
rs36408286 | snp | A/G | 0.260355 | 0.249785 | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88628015 | TTCAGAGATCGCATG[A/G]CCAGTCCACATTTAG | 74589 |
rs36411904 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88586603 | ATCCCACAGAATCCT[C/T]GTCATCTCATAGAGG | 74589 |
rs36412389 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Kbtbd12 | Mm_Celera | 6:88559561 | AAAACAGTGCCAGCA[A/G]CCGGGGACCAAGTCT | 74589 |
rs36414530 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88611215 | ATACAAGAGGAAGGG[A/C]TCCTTTTGCTTTTGC | 74589 |
rs36417068 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88587824 | AATAAGGAGCAGATA[A/G]AATATGTACAGAGTT | 74589 |
rs36428297 | snp | C/T | 0.18 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88600403 | CTCAATAAATATTAT[C/T]CTGCATGGAAAAAAT | 74589 |
rs36429878 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88582891 | CCTGTAGTGTCATAC[C/T]AATTGGCATAGCAGG | 74589 |
rs36430502 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88608449 | CAATGCAGGTATCCT[A/G]AATACATCTTATTTC | 74589 |
rs36431931 | snp | A/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88616742 | GCTGCTCCTCCTGAA[A/T]GGTCTTCATATCCAC | 74589 |
rs36432067 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88614961 | GTTTAGAAGGGATCT[C/T]AGATGTGGATCCTTA | 74589 |
rs36434452 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88611583 | AAACGTGCCGAGCCC[C/T]GAGACTTGGGGTTGT | 74589 |
rs36434666 | snp | C/T | 0.48 | 0.0979796 | synonymous-codon | Kbtbd12 | GRCm38.p3 | 6:88618433 | TGCTCCGATTTGTTT[C/T]GCAAAGTAATAAATT | 74589 |
rs36436524 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88622765 | ATCAGCTACCACACT[A/C]CAAAAAATATTCTTT | 74589 |
rs36437785 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88626879 | CCCCGCTGATGTCGT[C/T]TCCCTGATTTGTTTA | 74589 |
rs36444355 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88580798 | ACATTTTATAGGTGT[A/C]AGATATTTTATTATG | 74589 |
rs36446512 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88564874 | TGGGATCTAGGCATC[C/T]AGGGATGGGCTGAAC | 74589 |
rs36449199 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88562225 | AACTCATAAAGCTGG[A/G]AGCTCATTTGTTTAG | 74589 |
rs36452138 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88556134 | AACCATGGCTTGGGG[C/T]GAGAGAAAATCTCAA | 74589 |
rs36460386 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88549642 | TCATGTGTTCCTCCA[C/T]GCAGCCATGGTTGAG | 74589 |
rs36460491 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88562813 | TATTTAGTCTTAACA[A/C]TATTTGTCTTTTAGT | 74589 |
rs36461354 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88564527 | AGGCTCAGTCAACAC[C/T]AGCATCAGTCTTACA | 74589 |
rs36463440 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Kbtbd12 | Mm_Celera | 6:88549805 | CTGAGAATTCTGACT[A/C]TCCAGATTGGCCCTT | 74589 |
rs36464503 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88556379 | CCAGTAAAAGATGTC[G/T]GCTGAAGTATAGGTG | 74589 |
rs36481450 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Kbtbd12 | Mm_Celera | 6:88608012 | AGTGCTTCAGCAGCT[A/C]CAGTGCTCCTTCCCA | 74589 |
rs36481866 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88556212 | ATTCAGATTTTACCG[C/T]AGAAGGACAAACAGC | 74589 |
rs36483177 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88556081 | AAACAAGTAAAAGTA[C/T]GCATCCACCCAAAAA | 74589 |
rs36483544 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88564544 | GCATCAGTCTTACAC[A/T]GCACCTGAGAGTCGG | 74589 |
rs36492558 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88590085 | GGGAACTTTCTTTTA[C/T]TTAGTTCCTCTTGTG | 74589 |
rs36497957 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612807 | GACCCCAAAAGGACA[C/T]AAGGACACTGTGGCC | 74589 |
rs36499291 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88556832 | GACAGAGTCCTTTGC[A/G]CCAAGTTGAAAACTG | 74589 |
rs36516643 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88608581 | CTCTCTGGTAAGGAG[C/G]TACCACTGACTGCTT | 74589 |
rs36517498 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612473 | GCATGTAAATTCACT[A/G]TGAAGGTGGATAGTT | 74589 |
rs36518647 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88592296 | TATCCCACCTCAAAA[A/G]CAAAGGCGGCACAAG | 74589 |
rs36519957 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88582495 | TAAGATTTTCCTTTA[A/C]GATCCTAAACTTTAT | 74589 |
rs36526247 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88563084 | TGAATATTTTCAATT[G/T]CCATTTTCAAGTTAT | 74589 |
rs36528422 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88619906 | GACTATATAAGAAAG[A/G]AAGGCGGCAGTTATA | 74589 |
rs36536018 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88588185 | TCCCTGTCTGTCCAG[C/T]TCTTGGTCCTGTAAA | 74589 |
rs36539636 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88608309 | ATACGTCTATGATTT[C/T]ATAACAGTCTACATG | 74589 |
rs36545536 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Kbtbd12 | Mm_Celera | 6:88558964 | CTCTGTCTCTCTTGC[A/T]TCCATCTGTCTGTCT | 74589 |
rs36546854 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88561361 | CTGGTTACTTCTTGC[C/T]GCTTCCATGGACTTG | 74589 |
rs36548187 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88591823 | GACTTTTTCCTTTGA[A/G]CAGAAATCAAGGTTT | 74589 |
rs36555663 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88549503 | TCTTCCACTTACTAG[C/T]CTGTACATCTGCTAT | 74589 |
rs36557323 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88586402 | CAGTGTCAGGGTCAT[C/T]TGCTAGCTGAAAGCA | 74589 |
rs36562597 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Kbtbd12 | Mm_Celera | 6:88614041 | TGTTATGAGGTACTG[A/G]TTTTTAATTTTCATC | 74589 |
rs36564955 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88553780 | AAGGCCTTGAACATA[G/T]GAGGAGCTGGGCTGC | 74589 |
rs36566190 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88592335 | TCCACAAGGCCTGGT[A/G]TATTTCCTGAGGTGC | 74589 |
rs36573071 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88603252 | CACTGAAGGGCAGTT[C/T]GTTGACTCACACTAC | 74589 |
rs36574933 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Kbtbd12 | Mm_Celera | 6:88556172 | GAGATTACAGAGGGC[A/G]TGTACCTGCCCAGAA | 74589 |
rs36587169 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88560606 | TGTGTGTTATAATTC[A/C]TCTCCTCTCTTGGGA | 74589 |
rs36588399 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88559623 | CAGAAAAACTGTAAC[A/G]TAGATTTATTTCAAT | 74589 |
rs36590058 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88562250 | GTTTAGCTCTTCCCA[A/G]ATACAGATCTTCAAC | 74589 |
rs36591831 | snp | A/C | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88554679 | GACGAAGCCTTTAGC[A/C]TACAACTTTTGGGGC | 74589 |
rs36595625 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88557718 | AAGAATAGGAGAGGC[A/G]TGGCCAACCGACAGC | 74589 |
rs36617357 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612211 | GTTTACAACAAAGAC[A/G]CAATTGCCACCCTTA | 74589 |
rs36626649 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88554320 | TCCATGCCAAAAAGG[A/C]ACACAGCACAGTCAT | 74589 |
rs36632236 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88589353 | AGCATGACTTCCCCT[C/T]ACTCAAAACCAAGCA | 74589 |
rs36633681 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88621295 | TGGGGAAAGCCGACC[C/T]GATATCCCTTATTAG | 74589 |
rs36636030 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88556999 | ATTTACAGGGTTTCT[C/G]GGATGACTCTGAACT | 74589 |
rs36641776 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88615655 | ATTTATCAAACTTTC[C/T]AGCGGCTGTCTTCTA | 74589 |
rs36655468 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88587868 | CCAATTGCATAAGAT[A/T]TTCCAATCCACTGTG | 74589 |
rs36657404 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88611896 | CAAAATACTTTTGCT[A/C]TTTTAGTAATTAGAG | 74589 |
rs36666632 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88587853 | TTAGGACTTTGAAGT[C/T]CAATTGCATAAGATT | 74589 |
rs36673309 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88558842 | TGGGGAGACTGTACA[C/T]TGTTTTCCACTGATT | 74589 |
rs36678873 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Kbtbd12 | Mm_Celera | 6:88613720 | AGCAACACATTTTTT[A/T]AAAAAAAGATCAATT | 74589 |
rs36710506 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88606580 | CTGTCTGAACCACTT[C/T]CCTCAACAGACACAT | 74589 |
rs36717247 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88579147 | GTGTGGAAGTCTGCA[A/G]CAGGCCCTGATGCAG | 74589 |
rs36718758 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88585515 | AGGACAAATGGAGAA[A/C]AAGCGAAGCCTTTGA | 74589 |
rs36718957 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88617114 | TGTATATTTCATACT[A/C]ATGTAGTTAGCTTTA | 74589 |
rs36735266 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88559657 | CACCTCACTGTGAGG[C/T]GTGATCTGCATTCTT | 74589 |
rs36736151 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88559799 | TTCTCAGTCAGGGAT[A/G]TGACCTGCTCTTCTG | 74589 |
rs36736370 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88553990 | GAACACGTATGATGC[A/G]GGTGGTGTAACTTTC | 74589 |
rs36736533 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88565076 | TTTTACAAAGATGCC[A/G]TCGGTTCAATCCCCA | 74589 |
rs36742970 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88611728 | TATAAAAAAGCAAAG[C/T]GTGTTCTCTTGAGCA | 74589 |
rs36747761 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612600 | TATATAAGTACAAGA[A/T]TTTCAAGCTTATGAG | 74589 |
rs36750367 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88588654 | TGTGTGGCAGCAGAG[A/C]CCTGCAAGGTAAGAA | 74589 |
rs36755302 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88588447 | TTCTCTCCTATCTGC[C/T]CTGAGAAGTAATTTA | 74589 |
rs36762416 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88566708 | GACTTGCCTGCTCGT[C/T]GTGCGATCCAAAGCC | 74589 |
rs36773189 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88578862 | CATTATTGTCTTAGG[C/T]TTTCTGTTGTCATTT | 74589 |
rs36776980 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88590267 | GTAACTGAATTATTG[A/G]ATTGTTGCTGGTTTA | 74589 |
rs36778036 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612849 | CTCCGCTTTGACTTG[C/T]CATCACTTTGCTGGG | 74589 |
rs36788918 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88554803 | TACAGGCGCCCTGGC[A/G]TTTGTACTTTAGATT | 74589 |
rs36791758 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88556050 | GTTTAATCACAGAAA[C/T]ACGGAACCCTGTGTC | 74589 |
rs36800354 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88562971 | AATCCCTGGTTTAGA[C/T]TATTATTTTTTGTTG | 74589 |
rs36802144 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88590854 | TATTTTCAGTTAAAA[A/G]GTTCTTATCTGTCTC | 74589 |
rs36806874 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88610128 | GCTCACCCAGTGGAC[A/G]CTCTGCATGCCATGG | 74589 |
rs36812367 | snp | C/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88588877 | GACACAAGCAGAGTG[C/G]TTATAAGTCTTGACT | 74589 |
rs36812679 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88627833 | ATCTTTTAAGGGGAC[A/G]CGTCTTTCATTTAAT | 74589 |
rs36816154 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88563814 | GTCCTTCATAGCTCA[C/T]AGGCTTTGACAATAG | 74589 |
rs36817846 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Kbtbd12 | Mm_Celera | 6:88553667 | CTATCCCTAGGGTCA[G/T]GTGAACTCAAGGGTG | 74589 |
rs36821765 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88626457 | ACATCTACTTTTGAC[A/C]TCCACCCTCAAAGTT | 74589 |
rs36827863 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88559812 | ATGTGACCTGCTCTT[C/T]TGGTGGTAAGTGAAT | 74589 |
rs36838827 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88562246 | ATTTGTTTAGCTCTT[C/G]CCAGATACAGATCTT | 74589 |
rs36841661 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88592193 | TGCTTACCAGGAGGA[A/T]TAACCTCTCCTGATT | 74589 |
rs36843981 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612891 | ACAGTATTCTCTTGA[A/T]ATTGCTTATGCCCAG | 74589 |
rs36844166 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Kbtbd12 | Mm_Celera | 6:88584278 | AACATTGTGGAACTG[C/G]TCTTTTTCCTGTGAT | 74589 |
rs36859927 | snp | A/C | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612913 | TATGCCCAGCAAGAA[A/C]AGTTAACGTTTAGTC | 74589 |
rs36860644 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88587483 | TGCTCACTAACTCCT[C/T]GTTGATGGCAAGATA | 74589 |
rs36863798 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Kbtbd12 | Mm_Celera | 6:88562267 | TACAGATCTTCAACA[C/T]GTTTTGTTAGCCTTA | 74589 |
rs36877407 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88619138 | CATCAATTATTAACT[A/G]CTGCTGCAATAGTTT | 74589 |
rs36877947 | snp | A/C | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88559578 | CGGGGACCAAGTCTT[A/C]ACACATACGATCCTG | 74589 |
rs36883941 | snp | G/T | 0.231111 | 0.249285 | synonymous-codon | Kbtbd12 | Mm_Celera | 6:88617985 | CATAGCTCCTGTGCC[G/T]TGATCTGATTCCAGA | 74589 |
rs36892833 | snp | A/C | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612737 | GTTATCTGTACCGGG[A/C]TAAATTGGAAGGCAA | 74589 |
rs36901340 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88598287 | AGGGATGCCCTCTCA[G/T]GTGGTTGTAGAGGTG | 74589 |
rs36908845 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88562383 | TCTCTGTGTAGCTTG[A/T]GGATGGTGGTGAACC | 74589 |
rs36909581 | snp | A/G | 0.336735 | 0.234472 | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88628316 | GCTAGCTTAAAACGA[A/G]CCAGAATGGCTTTAG | 74589 |
rs36921603 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88623157 | ACTTGGGATTTCTTC[C/T]GAGAATTATATAAGA | 74589 |
rs36932022 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Kbtbd12 | Mm_Celera | 6:88618265 | CCATCTCAGAACCAA[A/G]TCCAGAATGCTCTCT | 74589 |
rs36935546 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Kbtbd12 | Mm_Celera | 6:88556908 | TTCCCTGTCCTCTGA[C/T]CCGGGTGCTGAATCC | 74589 |
rs36936848 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88589222 | ATTAATAAGTCAGTG[C/G]TGGCTCTACAAGTAC | 74589 |
rs36937640 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Kbtbd12 | Mm_Celera | 6:88558039 | AAAATCACTGTATTA[A/G]TCTTAAACGGAAGGT | 74589 |
rs36945504 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88565365 | ATATGCAAAACCCCC[A/G]CTTTTTTCACATACA | 74589 |
rs36950424 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88603007 | AGGAGAATGAGCAAC[C/T]GTGATGGGATCTGGA | 74589 |
rs36954508 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88558003 | ATTGTTCCCAGGAGC[C/T]TGTTATTCCAGACAT | 74589 |
rs36957639 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Kbtbd12 | Mm_Celera | 6:88594469 | CTGGTCTCTTCTATA[C/T]CAGCCCAGGGCTGGC | 74589 |
rs36995038 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88589767 | CAAAATCCCAAAGTT[G/T]CTTGCCTTGCTAAAC | 74589 |
rs36996855 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88611979 | AAGATAATAGGATTA[A/G]CATAAATTACTTGAG | 74589 |
rs37003734 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88565386 | TTCACATACAGGGAG[G/T]AAACGTCATATGAAT | 74589 |
rs37008144 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88591430 | CAAAGGTCTGCGTTG[A/G]GTCCCTAAATGAGAA | 74589 |
rs37009927 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88590042 | AGGGAGAAAGCCAGG[A/G]CCTCTGAGCACTCGT | 74589 |
rs37012946 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88594088 | GGTCTGGTCTTCTTC[A/G]AACTGCTAAGGATGC | 74589 |
rs37023205 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88578785 | AGTTGAAGCTGCTTT[C/G]TAGTTGTTAAATTCT | 74589 |
rs37024249 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88563748 | TCTACGGTGTTTCTT[G/T]GCTTTTCACGTTCAG | 74589 |
rs37026893 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88560380 | GGATGGCTCAGCAGT[A/G]CTCTTCCAGAGGTCC | 74589 |
rs37028597 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88585609 | CCCAGCTCTAATAAC[A/G]ACCGCATCCATCTCT | 74589 |
rs37029560 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88615069 | ACTAGTTTATGGCTA[C/T]CTTTTGACTTTCTTC | 74589 |
rs37030263 | snp | C/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88594446 | TGAGTAGACATACTG[C/G]ACTCATCCTGGTCTC | 74589 |
rs37030297 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88606548 | TTGCCTGGGTTTGTA[C/G]TTGGCACCCTTCCCT | 74589 |
rs37037416 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88595487 | GCATATATTATTCAA[A/G]AAGCATAATCACTAG | 74589 |
rs37041570 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88611604 | TTGGGGTTGTAAGTA[C/T]TCTGTCAATATCAGA | 74589 |
rs37042835 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88589485 | TCCCTATTCTTTCTT[C/T]ATTTTATTCCTACAA | 74589 |
rs37052073 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88584197 | GACCATTTCCTGGGA[A/T]TCTAGAGGTGGTCAG | 74589 |
rs37061392 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88616800 | AGGATGCTCCTTTAG[C/T]CTGTGACATGCTTGA | 74589 |
rs37062176 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88588675 | AAGGTAAGAAGATGG[C/T]GAGTCCCTTCTCTGA | 74589 |
rs37066940 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88564139 | GGGAACTTGAGTTTC[A/C]TCCTTAGGGCCTGCA | 74589 |
rs37071630 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Kbtbd12 | Mm_Celera | 6:88558265 | GAAATATCATCACAC[C/T]AGCAAGGAAAAGGCA | 74589 |
rs37076257 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88566562 | ATATAAAAAAGTTAG[C/T]ACGCTATCTTTTTGT | 74589 |
rs37080378 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88549901 | CAGGGAGAATGAAGC[A/G]CATAAACCGTCCGTA | 74589 |
rs37080439 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88614578 | AATATGGAAGAAATC[A/G]GGGTTTTAAGGCAGA | 74589 |
rs37081926 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88619356 | AGGCTATACTCAAGT[C/T]CTCTACAACATGTAA | 74589 |
rs37088742 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Kbtbd12 | Mm_Celera | 6:88553878 | AATCTAAATAAGCCC[A/G]AACACTCACTTGTCC | 74589 |
rs37090166 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88557782 | ATTCTGCAAGCTGAT[A/G]TAACTGCTCCTGCTC | 74589 |
rs37097633 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612653 | ATAATGAGGCAAATT[A/T]TATAGAATAAGAGAA | 74589 |
rs37111040 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88573623 | GGAGTTATTCATGTG[C/T]TGGCCAGCTCCATTT | 74589 |
rs37118803 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88576594 | CTCCTTCCTACTCGG[C/T]TGCTTCTCCAGGCAC | 74589 |
rs37129231 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612687 | ACAGGCAAAAATAAA[A/T]TTATATTACAGAGAC | 74589 |
rs37133219 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88585472 | AATGCAATAAGACAT[A/T]TAAAGACCTTTTGGG | 74589 |
rs37133723 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88558456 | GGCTCTGCTATACCA[A/G]GGAGTAAATGAGATA | 74589 |
rs37143813 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88611106 | AAGATGCCATAAAAA[C/T]AGTTTTGCCCTCTAC | 74589 |
rs37153609 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Kbtbd12 | Mm_Celera | 6:88554610 | CTGAAAGACCTACCC[A/G]TAGGCCTCATACATC | 74589 |
rs37168840 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Kbtbd12 | Mm_Celera | 6:88602379 | GAGAATTTAAAGTGA[A/T]AAGCCCTCCCTGAGA | 74589 |
rs37188763 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88548752 | CCTCCAAAGTCAGGC[A/G]TCTATCTTTACTGTC | 74589 |
rs37189062 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88599343 | ATACATGGCTGTCTG[C/T]AGTGTGATCTTATCT | 74589 |
rs37195503 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88564100 | AAGATTGCTCAGTGG[A/G]TAAAGGTACTTGCCA | 74589 |
rs37196411 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88554370 | CTAGCACTGTGATGA[A/G]ACATCCAAGGCAAAT | 74589 |
rs37197530 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88625372 | TTCCAGTTCCAAAGC[A/G]AAATGTTTTATTAAG | 74589 |
rs37203244 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88583255 | TGTTTGTTTCTGGTA[C/G]TTACTGTTGGCTCTT | 74589 |
rs37204755 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88594632 | GTTCAGACCTTCTGA[C/T]AGGTATCTGCCAAGT | 74589 |
rs37224934 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Kbtbd12 | Mm_Celera | 6:88548423 | TCTGTGTGCACGGGC[A/G]GAAGCACAGTCTGAG | 74589 |
rs37235227 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Kbtbd12 | Mm_Celera | 6:88584157 | GGTTTTGCCTTTTTC[A/G]GCCTCTGCATGAAAC | 74589 |
rs37235772 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88559761 | GCGAATCAACAGAGA[A/G]GTGTCCAGCCTACTT | 74589 |
rs37256623 | snp | G/T | 0.231111 | 0.249285 | synonymous-codon | Kbtbd12 | Mm_Celera | 6:88618544 | GGCAGCCATGGCTAC[G/T]GTCTGAACGTTGGCG | 74589 |
rs37259240 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88580871 | AAGTTAAAAATTAGG[A/G]TCACAGATATGAGGA | 74589 |
rs37281955 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88588735 | TTGCAACTAGTTAGA[C/T]CAGGGAGTGAAGCAA | 74589 |
rs37283290 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88586677 | TCCGAAAGCCAGACT[C/T]TTGCCAGTGCCTCAC | 74589 |
rs37297067 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88563757 | TTTCTTGGCTTTTCA[C/T]GTTCAGAAGTTTGGT | 74589 |
rs37307629 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Kbtbd12 | Mm_Celera | 6:88553860 | AAGATGGTTGCTGAG[A/T]GAAATCTAAATAAGC | 74589 |
rs37309132 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88626925 | CCTCAGATGTACATA[A/C]GGCTTGCAATAATGA | 74589 |
rs37310299 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88561849 | ATGTCTACACAGTCA[C/T]ATCCTGTTTCAAAGC | 74589 |
rs37319081 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88556033 | GATAGTATGATCAGT[A/G]AGTTTAATCACAGAA | 74589 |
rs37359025 | snp | C/G | 0.142012 | 0.225474 | missense | Kbtbd12 | Mm_Celera | 6:88547862 | CCACAACGTTCCACT[C/G]GTTCTCCCAAGGGTC | 74589 |
rs37359118 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Kbtbd12 | Mm_Celera | 6:88559379 | CTGAGCTCAGAGTTT[C/G]AGGGAACATAGTCCA | 74589 |
rs37359952 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88588623 | CTAGCCAAGAAGTCA[C/T]GTAGAAGAGGGTTTG | 74589 |
rs37360105 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88588131 | GGAATGAATGAATGA[A/G]TATGAAATGTCCCTT | 74589 |
rs37362745 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88587521 | GTGACAAGGAGTTTG[A/G]AAAGATTGACAAGGC | 74589 |
rs37364450 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88616542 | GAACAGAATAAAACA[C/T]GTGACAGCATTGATA | 74589 |
rs37375533 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88617584 | AGATGTGATCCCTCA[C/T]AGTACTTCTTCAACT | 74589 |
rs37376562 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88586177 | TCAGAATCAGCTAGT[C/T]AGTCTACTATGAAGG | 74589 |
rs37378260 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88621613 | AAGTTGCTTAGGGTA[G/T]CTGTAATTATGTACA | 74589 |
rs37378353 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88588028 | TCACTGAATTCATCA[A/G]GCAGACCTTCATTAT | 74589 |
rs37392226 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88617268 | TTCTTCAAAAGCTCT[A/G]TAATGCTGAAGGTTT | 74589 |
rs37402804 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Kbtbd12 | Mm_Celera | 6:88554246 | CAGCCTCAAGATGGT[A/G]CCCCACTACAGCCTT | 74589 |
rs37405791 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88595009 | TTTAAAAAATTGCCA[C/T]GAGACCTTTACTGTG | 74589 |
rs37409986 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Kbtbd12 | Mm_Celera | 6:88623908 | CTCAAAAGAATATTG[C/T]ATAATGGAAAAATGA | 74589 |
rs37412639 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88615696 | GAAAGGAAGCCAGAG[A/T]TCCTGGAATTGCAAA | 74589 |
rs37413385 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Kbtbd12 | Mm_Celera | 6:88580776 | CTTAAATTTATAAGC[C/T]TATGGGACATTTTAT | 74589 |
rs37419466 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Kbtbd12 | Mm_Celera | 6:88554192 | CTCCCTCTGTTTGAG[A/G]AGCAGCCTGCTCCCC | 74589 |
rs37432976 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88621700 | AATCTTGGATCCTTA[C/T]TCCTCCTTCATAGAA | 74589 |
rs37434648 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Kbtbd12 | Mm_Celera | 6:88584297 | TTTTCCTGTGATTTT[C/T]GGGATTAATAAGCGA | 74589 |
rs37438594 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88560075 | AGTTAAGAATTTCAT[A/C]AAATTGAAAGAATGC | 74589 |
rs37447962 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88584085 | ATGTAGGCAGGAAAT[A/T]TGTCAACATGTATGC | 74589 |
rs37464543 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612347 | GAGGCCCAGTGAGAC[C/T]GACTCAGAGACTACA | 74589 |
rs37464545 | snp | C/G | 0.18 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88553726 | TCCTGGTGTAAGGCT[C/G]ACAGATGTGTGCCAA | 74589 |
rs37468194 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88583429 | ACTGTGAAGTGGTAA[A/G]CCTCACTGCCCAAGG | 74589 |
rs37470346 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88608545 | GAGGCTAAAGCTTTC[C/T]TCACATTAACATACT | 74589 |
rs37470352 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88578280 | CTGAGGCTCCAGAGA[A/C]GTGCTTTCCACTCTG | 74589 |
rs37502796 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88577483 | CTTGGGAAATATCAA[A/G]TCACATGGTTTTGCT | 74589 |
rs37504161 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Kbtbd12 | Mm_Celera | 6:88557362 | TTAAAGATGAACACA[A/T]TGGTATTTGTCTATC | 74589 |
rs37559700 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612770 | ATAAAGGACACCACT[A/G]TAAATGCCAAAGATC | 74589 |
rs37559862 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88611643 | TATGTGCAGGGGGCT[A/C]ACATGCTGATTTATA | 74589 |
rs37563198 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88561259 | GAGTGGCTTTTGCAT[C/T]GGTTCACCTCGCAAC | 74589 |
rs37579785 | snp | C/T | 0.336735 | 0.234472 | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88628001 | TTCGTATAATATGTT[C/T]CAGAGATCGCATGGC | 74589 |
rs37587712 | snp | A/G | 0.260355 | 0.249785 | downstream-variant-500B | Kbtbd12 | Mm_Celera | 6:88547661 | TTTGCATTCTGAGCA[A/G]CCCAAGCATCGCTGC | 74589 |
rs37590144 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612837 | CCCACTGCTGACCTC[C/T]GCTTTGACTTGCCAT | 74589 |
rs37597581 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88554074 | GCTCAGGCACCCAGA[C/T]TCCTTTGGTTTCTCA | 74589 |
rs37598455 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88561813 | CTCTGTAAGTTCAAG[A/G]CTGGCCTGGTCTACA | 74589 |
rs37603659 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88591612 | CTAGATAATCCAGGT[A/C]CTGCCCTCCTAACAT | 74589 |
rs37607660 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88587133 | TGTCACTGTAATGCC[A/G]CATTTCCTGTTACTG | 74589 |
rs37613834 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88615651 | GAAGATTTATCAAAC[C/T]TTCCAGCGGCTGTCT | 74589 |
rs37614861 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88559311 | TGCCATTGTTGTCAT[A/C]GATGTGACTGAACAC | 74589 |
rs37622359 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88603159 | CAGAACTAGTTTTTG[A/G]TAAGGTTACTCAATT | 74589 |
rs37622441 | snp | A/C/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88602909 | GCTGACCTAGCAAAT[A/C/G]TTTCCACAAATGCTT | 74589 |
rs37637969 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Kbtbd12 | Mm_Celera | 6:88561971 | TGTCTGCTTGTCACC[A/G]GATCCCACTGGGTTA | 74589 |
rs37651374 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88621436 | CCTGAGACAGCAGCA[A/G]GACAAAATAAATTCA | 74589 |
rs37670869 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88588183 | CTTCCCTGTCTGTCC[A/T]GTTCTTGGTCCTGTA | 74589 |
rs37696257 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88626349 | TAGCTTTGGAGATTC[C/T]GATTTTGCTTAAACC | 74589 |
rs37715148 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88555866 | AAGACGACGTTAATG[A/G]GCACTAGTTGGTAAT | 74589 |
rs37717291 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88620847 | CTACCTGATGGGCTG[C/T]TTGGTACTACATTTG | 74589 |
rs37722616 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88602452 | GCCACAGGCATGCTC[A/G]ACTTTGGTGGTCCTC | 74589 |
rs37722919 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612383 | ACAACCACCTTCTTT[A/G]CTGCTTTAACTTTCC | 74589 |
rs37755287 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Kbtbd12 | Mm_Celera | 6:88557910 | ATGAAAGTAGGCAGA[C/G]CTCTCATTGCTGCCT | 74589 |
rs37755598 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88562783 | CTTTTAGACACCATA[C/T]AGTTAGATGCAGTTT | 74589 |
rs37764726 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88603403 | TTGTTCACAGAACAT[C/T]GATAGTTTGCCTTGT | 74589 |
rs37797400 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88562124 | TTGTCTACATGCACA[A/G]GCAGTCTGAACAAGA | 74589 |
rs37800736 | snp | A/G | 0.142012 | 0.225474 | synonymous-codon | Kbtbd12 | Mm_Celera | 6:88586796 | TGCTCCATGAAATCC[A/G]CCGCAGACATAGAGC | 74589 |
rs37816545 | snp | A/C | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88609147 | CTATGTTAAGTCTTC[A/C]TGGCCTCCATAATGT | 74589 |
rs37816637 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88611877 | TTTCTAACCTATAAA[A/G]TTTCAAAATACTTTT | 74589 |
rs37819322 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88588503 | TGCTGTGTTTTGGAG[A/G]AAGGGTCACATCGGC | 74589 |
rs37823829 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88598187 | AGCAGTAGGTTGTGT[A/G]AATGTGTAGCATGAC | 74589 |
rs37841102 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88613748 | ATTTTCTAAAACTGC[G/T]TTGACATATTCAAGA | 74589 |
rs37843670 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88558067 | GGTGATAGCAGATAG[G/T]CTCTCCCTCAGAGAG | 74589 |
rs37856658 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88616665 | AGATAGAAAGGGCAC[C/T]AGCACAAATCCTGTG | 74589 |
rs37862375 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Kbtbd12 | Mm_Celera | 6:88626788 | TTCTGCCATCACCAG[A/C]TTTCCCCAGTCCTAC | 74589 |
rs37871878 | snp | G/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88615035 | TGATTACTAGGTATA[G/T]TATAAAGCCCCTGAG | 74589 |
rs37878058 | snp | G/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88620215 | CACTGCCTCTTCAGT[G/T]TTGCTTCCATAACAC | 74589 |
rs37880672 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88588839 | TTCCACCTTAAATCC[C/T]CTCAGAGAGGTTGCC | 74589 |
rs37892918 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88615308 | GAAATTAAATGTCTC[A/C]GAAAAATATAGAAAA | 74589 |
rs37898118 | snp | G/T | 0.336735 | 0.234472 | downstream-variant-500B | Kbtbd12 | Mm_Celera | 6:88547336 | CCAGCTTTCCTACTT[G/T]ACAACCTTTGACTGT | 74589 |
rs37908509 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88580972 | TGGCAAACGGTCTCT[C/T]CTTCCCCAAGGTCTA | 74589 |
rs37909403 | snp | A/C | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88597892 | CCAGAAGCTCTTTCC[A/C]TTGAAACTCAGTGTC | 74589 |
rs37914324 | snp | C/T | 0.5 | 0 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582354 | CCCAGGCTGCAGCTA[C/T]GTTGTTAGCTCATTT | 74589 |
rs37924400 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88611121 | TAGTTTTGCCCTCTA[A/C]GAATTAATCTTATTT | 74589 |
rs37924909 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88625238 | AAAGAGCAGAAAAGT[A/T]ACAAGGACAGGGCTC | 74589 |
rs37927462 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88555190 | TTTTGCTTACTACCA[C/T]GAGAACATCTAAAGG | 74589 |
rs37934475 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88580964 | AAGCTGTCTGGCAAA[C/T]GGTCTCTCCTTCCCC | 74589 |
rs37937187 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88554725 | GTAATAGAAAGGACA[C/T]GGAGGTACAGGCCTC | 74589 |
rs37943669 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Kbtbd12 | Mm_Celera | 6:88550365 | CATATTTGGTGATTC[C/T]TCCCTTTGGAGAGTG | 74589 |
rs37950357 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Kbtbd12 | Mm_Celera | 6:88558494 | GAGGTTTGAGGTAAA[G/T]AAGGCAGTGGAAGCC | 74589 |
rs37958469 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88615725 | AAGAGTATTTTCACT[A/C]ATTTTTAGTTGTATG | 74589 |
rs37964437 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Kbtbd12 | Mm_Celera | 6:88624993 | GTAAAAATGATCAAC[A/G]TCAAAGCTTTGGATT | 74589 |
rs37969440 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88550335 | CCTAAATAATGCAGA[A/G]CTAGAGTAGACAGAC | 74589 |
rs37975013 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88620864 | TGGTACTACATTTGG[C/T]TATTGTAATTAAAAA | 74589 |
rs37976942 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88609101 | AAACATCCTTTAATC[A/G]GCTTGCTTCCGTGTG | 74589 |
rs37977394 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88549988 | GACAGGCAGGCATAT[C/T]ACCCCTTCTCACTCA | 74589 |
rs37977409 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88610699 | GAGAAAGAAGATTCA[C/T]GCTCTGAAGACTAAG | 74589 |
rs37981412 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88562999 | TTGTAATATTAATGG[A/T]CTTGAGTTTAGGTCT | 74589 |
rs37982649 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88617461 | AATTTTAAAATATGA[A/C]TGACTTATAAATATT | 74589 |
rs37983850 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Kbtbd12 | Mm_Celera | 6:88606122 | ATGTATTTACTGAAA[A/T]TTTTACATTATTCCC | 74589 |
rs37984589 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88594179 | ATGCAATGGTGAACC[A/T]TTCACCCCAGCTGAG | 74589 |
rs37986251 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612509 | AAATGTACCTACCTC[A/C]AGGTAATGGCAATAC | 74589 |
rs38004221 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Kbtbd12 | Mm_Celera | 6:88624040 | AAAGTATAGGTCACA[C/T]ATTATGATGACATAA | 74589 |
rs38004535 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88584121 | CCTGATTGGACCTGA[C/T]AGGAAATTCGGTGGC | 74589 |
rs38033017 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88610604 | CCAAACACAGTAGCC[A/G]TCCAATCAGCCTCAT | 74589 |
rs38034997 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88608682 | AGGTTCATAGTAATT[A/T]GCAGGGATCTCCAAG | 74589 |
rs38051693 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88608332 | TCTACATGGTGATGC[C/G]TAGGCCTTCAACACA | 74589 |
rs38064029 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88598096 | AAGCTTTTGTCTTCA[C/G/T]GGCCTGCAGCAAGAG | 74589 |
rs38068159 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88558519 | GAAGCCCATGTATGC[A/G]GCAGACTGCCTTGGG | 74589 |
rs38072279 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88584272 | TGGCTCAACATTGTG[A/G]AACTGGTCTTTTTCC | 74589 |
rs38088710 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Kbtbd12 | Mm_Celera | 6:88618343 | GTGAGCTTCGATGTC[A/G]AGTATTTCTCCATGA | 74589 |
rs38090300 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Kbtbd12 | Mm_Celera | 6:88550561 | CCACGTGCACATACA[C/T]TGATTCTGCATCTGT | 74589 |
rs38103039 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88615233 | GTACTTTTCCAATTG[C/T]AATTTGAGACATTCG | 74589 |
rs38108233 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88625600 | TAACAATTCTAATGC[A/G]TACACGTAATACTCT | 74589 |
rs38124766 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88563677 | TTGGCTTGAGAAATC[C/T]GGCCATTTTGATATC | 74589 |
rs38140948 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88615507 | CAGTTAGTCATCTAA[A/G]CAGAGTTTCTCCCAC | 74589 |
rs38148462 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88603348 | GGTGATAGCAACCCA[C/T]TCCCTGTTTGGTAAC | 74589 |
rs38159430 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88575971 | ATGCTGGCTTCCTCA[A/G]CCTATGTTAGGTGGG | 74589 |
rs38159570 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88619159 | GCAATAGTTTCTAAT[C/T]GTCAGTGGTTCCCAC | 74589 |
rs38175902 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88624587 | CTGGAAAATACAGAA[A/G]CCTCCTCTCTGGTCT | 74589 |
rs38183386 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88554144 | GATGATGGTTGTTCA[C/T]TAGTCAATCCCAGAA | 74589 |
rs38222126 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88558339 | CCCCAAAAATAGATG[C/T]ACCACATGCGGCAGT | 74589 |
rs38232126 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88617159 | AGAAATATTTACAAT[G/T]AGATCATAAAGTAAA | 74589 |
rs38233605 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88577797 | ACTAACATTTGGAGG[C/T]CTCCGTGAGATTAAA | 74589 |
rs38236538 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88593633 | AGCTTCCTAACATCC[C/T]GAATCAGAAGCATTT | 74589 |
rs38237369 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Kbtbd12 | Mm_Celera | 6:88623080 | CCAGAATCTGACTCC[G/T]TATCTACTGTAATGA | 74589 |
rs38240331 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88586245 | CATTGGCCTCTAGAT[C/T]CATGCATGCTTAAAA | 74589 |
rs38244669 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88559298 | AGTTTCTGTTCTGTG[C/T]CATTGTTGTCATCGA | 74589 |
rs38256323 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88556305 | CAAGGCAGTAGGATC[A/G]TTAGGTAATACAGCA | 74589 |
rs38259531 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88611852 | TCTTTATATTTTTAC[C/T]CTATAAAAGTTTCTA | 74589 |
rs38280648 | snp | A/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88617244 | GTTCCTTTTACTATA[A/T]TTGAGGCATTCTTCA | 74589 |
rs38288609 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88560305 | GTACCACAAAGTCCA[A/G]CTAGGAATGTTTCTA | 74589 |
rs38331959 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88624562 | TGTAGGCAGCTCTAC[G/T]TATGAGTGACTGGAA | 74589 |
rs38382048 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88588301 | ATTTACTATGAGTGG[A/G]TCTTAAGCCAGGTTT | 74589 |
rs38395047 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88583387 | GATTTAGCTCAGGAT[A/T]CAACTCAAGGGTGTG | 74589 |
rs38409851 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612960 | GAAGTGATTGTGCCA[C/T]TACGGAATCAATATT | 74589 |
rs38469713 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88594610 | CTGCTATCAGGCTCT[C/T]AGCTCCGTTCAGACC | 74589 |
rs38489475 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88601240 | GCCTTTAAGAAATGA[A/G]GCCTTGGCACCTGGG | 74589 |
rs38556458 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88616772 | CTTTGCAGTCTACGG[A/G]TAATTCTGAGGAAGG | 74589 |
rs38575816 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88608949 | TTATAGGTGGCAAGA[C/T]TTACTGGGACGGTTA | 74589 |
rs38579577 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88579371 | AATAAACGAGCTTAC[C/T]GCGTTCTGTGCCTCT | 74589 |
rs38661036 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88559837 | GTGAATTGCCTGTCA[A/G]TGAAAGCAAAGGATT | 74589 |
rs38720278 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88561776 | TTTAATCCCAGGACA[C/T]GAATGGCAGAGTCAG | 74589 |
rs38731991 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88563158 | ATTTTAGTAGCTACT[A/G]TAAGGCTCATTATAC | 74589 |
rs38745442 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612556 | TGTACTATGTCTGAC[C/T]TACAGCACAGGTAGA | 74589 |
rs38762178 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd12 | Mm_Celera | 6:88594029 | TTAGGGCATTAGTGA[C/T]AGAATCTGCTGCAGC | 74589 |
rs38791479 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88560848 | CTTTTCAGATAGTTT[A/G]TAGCGTAGTATCTCA | 74589 |
rs38794292 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88565113 | CCTTTGAAAAGCAGG[C/G]TTCTTGGGTACCAAA | 74589 |
rs38837372 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612013 | GTATTTACATATTTA[C/T]TAACTTTATATATTT | 74589 |
rs38920247 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88619882 | GTGAGATGGTGACTG[C/T]GGCAGAGTGACTATA | 74589 |
rs38930251 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88594493 | GGCTGGCTAATGCTG[A/C]ACAGGGTTAGTAAAT | 74589 |
rs38977622 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88548355 | GTACCGACAGAATAC[G/T]CGGCTGTTGTCAGGG | 74589 |
rs39048755 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88612926 | AACAGTTAACGTTTA[C/G]TCACAACACACTTTC | 74589 |
rs39088956 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88625251 | GTAACAAGGACAGGG[C/T]TCCAAAAATCTAGTT | 74589 |
rs39093837 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88616421 | ACAGGACCCTGGCTG[A/C]ATCTAAGATAGTTTA | 74589 |
rs39128651 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Kbtbd12 | Mm_Celera | 6:88598084 | CCTTGCTGTTGAAAG[A/C]TTTTGTCTTCACGGC | 74589 |
rs39137904 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88567147 | TTTTCAGATTCTCTC[A/T]CTGTTGCGGCCGCCA | 74589 |
rs39180039 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kbtbd12 | Mm_Celera | 6:88603112 | GCACTCCTAGGAAAA[A/G]GCGATGGTCCTTAGA | 74589 |
rs39217045 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88577860 | TGAAGCTTGGATCTT[C/T]AAGAGGCTGGTAAGC | 74589 |
rs39328274 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kbtbd12 | Mm_Celera | 6:88583039 | AATTATTGTTTCTAT[A/G]CAAACCATTCAGGAT | 74589 |
rs39374070 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88550306 | GGAAGTATGTGTGGC[G/T]TCTACTGAAAGAGCC | 74589 |
rs39407614 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Kbtbd12 | Mm_Celera | 6:88548392 | GATGTTCTGATGCCA[G/T]GGAGTTGTCTTGATT | 74589 |
rs39408027 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88556286 | CACCTGGGATCTGGT[A/G]TGACAAGGCAGTAGG | 74589 |
rs39445590 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88564291 | ATGTTCAGCCTCCAT[C/T]TCAAATTCTATACTT | 74589 |
rs39462162 | snp | G/T | 0.124444 | 0.216185 | utr-variant-5-prime | Kbtbd12 | Mm_Celera | 6:88618911 | TTCCTGAGGAGCTAT[G/T]TGCATTTCTGATTAC | 74589 |
rs39470335 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88560485 | TGTTGAGTTCTATTC[C/T]CTCCGTGGAGTCTAC | 74589 |
rs39572895 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88565321 | GATGTTGTGAAAGTA[C/T]CCGGCAGGGTGCCAC | 74589 |
rs39605597 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88562391 | TAGCTTGAGGATGGT[A/G]GTGAACCCAGACTTT | 74589 |
rs39730442 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Kbtbd12 | Mm_Celera | 6:88625676 | GCGCAGATAACATTT[C/T]CTGAAGTAAAGGACT | 74589 |
rs39749490 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Kbtbd12 | Mm_Celera | 6:88563580 | TGGCTTGGCTTTGCC[C/T]TGGTTCCTAAGCAGC | 74589 |
rs39832517 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88596092 | GCACCTGCATGGTTG[G/T]TCAGTATACCTGTAC | 74589 |
rs39845718 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd12 | Mm_Celera | 6:88615911 | TCACTTATTTCATAA[A/G]CCAAAGTGGGAAGAT | 74589 |
rs45904453 | snp | C/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88609655 | CTGGAATAGAAACCC[C/T]GACTAAGACACTGGC | 74589 |
rs45907015 | snp | C/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582723 | GCCTGACTCCCCTGA[C/T]AGTTTCTGACAATTT | 74589 |
rs46150507 | snp | C/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88580570 | GGGATTAAAGGCGTG[C/T]ACCACCACGCCCAGC | 74589 |
rs46457858 | snp | A/G | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582623 | AACTTACTGAAAGCC[A/G]AGGCAAACCAGTCCA | 74589 |
rs46504938 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88582611 | TGCTGAGCTCTGAAC[C/T]TACTGAAAGCCAAGG | 74589 |
rs46565459 | snp | A/C | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582641 | GCAAACCAGTCCAGC[A/C]GATGTGATTGTGCCC | 74589 |
rs46913475 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88581137 | TGCATGGACTGTATT[C/T]GTGATTTAAGAACTG | 74589 |
rs46947035 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88564596 | AGTGCATTTTCTGCC[A/C]GTTGATTTGGGTCTG | 74589 |
rs47058920 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88564477 | TGTTGTGGGAATAAA[C/T]GAACAAACTTGTGCA | 74589 |
rs47459032 | snp | C/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582652 | CAGCCGATGTGATTG[C/T]GCCCTGTGCCTTCAG | 74589 |
rs47667668 | snp | C/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582584 | TCCAGGAATCAGCTG[C/T]AGACTGTAAACTGCT | 74589 |
rs47785762 | snp | A/C | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88581342 | AGCCTAAAGCAAGTA[A/C]CTAAAAACAAGCAAG | 74589 |
rs47789352 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88619473 | ATTAAACTTTGACAT[C/G]GGAAAGATTATCCAG | 74589 |
rs47980343 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88554469 | CCATTGTTTTTGGTC[C/T]TATGGTGACAGCAGA | 74589 |
rs48005595 | snp | C/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88625516 | CCTGCCTCTGTCTCC[C/T]AAGTGCTGGGATTAA | 74589 |
rs48038897 | snp | C/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582622 | GAACTTACTGAAAGC[C/T]AAGGCAAACCAGTCC | 74589 |
rs48150611 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88624068 | TAAATATATGATGAT[C/T]TTGGTAGAGTGTATC | 74589 |
rs48339410 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609035 | CTCCCCACTTCTGGC[C/T]TCTCCTGGCCTTTGC | 74589 |
rs48407516 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88581172 | TTGAAACTAGAAGAG[C/T]TTTAATTCAGAAATT | 74589 |
rs48493490 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88564762 | TGGAAGGAATGAGAA[C/T]GAGGTGGGAGCGTTG | 74589 |
rs48557690 | snp | C/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88592552 | ATTCCAGGACTCCTA[C/T]AGGGGAGTGGGAGGC | 74589 |
rs48710198 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88624794 | TGCTCTTCCAGAGGT[C/T]CTGAGTTCAAATCCC | 74589 |
rs48750926 | snp | A/G | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88581283 | ATTTGATTAAATTAC[A/G]GAAATATGTTTTATT | 74589 |
rs49104514 | snp | A/G/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582687 | GTCAGCTACCCAGAT[A/G/T]CGGGTGGTGAATACA | 74589 |
rs49156374 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609584 | ACAGCAATGTGGAAA[C/T]ATAAGCTGAATAAAC | 74589 |
rs49228664 | snp | A/G | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88609796 | CGTGCCTTCTATAGT[A/G]GACTGAAATCCCTCT | 74589 |
rs49247041 | snp | A/G | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582321 | GCTTTGTCAACAACA[A/G]GCAACTAGCTCCTTC | 74589 |
rs49394933 | snp | A/G | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582613 | CTGAGCTCTGAACTT[A/G]CTGAAAGCCAAGGCA | 74589 |
rs49480404 | snp | A/C | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88601941 | GTCAGAGGGTGGATC[A/C]GGAGGGGGATAAAGT | 74589 |
rs49560745 | snp | A/G | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88580571 | GGATTAAAGGCGTGC[A/G]CCACCACGCCCAGCA | 74589 |
rs49639420 | snp | C/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582520 | CTTTATCTTTTGTTC[C/T]CCGTCTATATCCGTC | 74589 |
rs49717770 | snp | C/G | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582829 | GTCCCCATCAGACTG[C/G]AATGCTGTCAAAAGG | 74589 |
rs49735513 | snp | A/G | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88605729 | AGGACCAACACCCAG[A/G]GCTGTCCTCTGACTT | 74589 |
rs50122324 | snp | A/C | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582522 | TTATCTTTTGTTCCC[A/C]GTCTATATCCGTCTC | 74589 |
rs50122462 | snp | C/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582337 | GCAACTAGCTCCTTC[C/T]ACCCAGGCTGCAGCT | 74589 |
rs50223262 | snp | C/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88609997 | GCCACCCTTGTCTTA[C/T]CCCAAACTGCCACTC | 74589 |
rs50337111 | snp | A/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88581359 | TAAAAACAAGCAAGG[A/T]TTATTTAGCTCAGAT | 74589 |
rs50654475 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88602726 | TAGACCTGGAAAGAC[C/T]TAGATCACTCCACCA | 74589 |
rs50683963 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609585 | CAGCAATGTGGAAAC[A/G]TAAGCTGAATAAACC | 74589 |
rs50691263 | snp | A/G | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582287 | TCTCAGATCTCTGAT[A/G]GCATTGATGGCTAGG | 74589 |
rs50742448 | snp | G/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88589808 | GGTGGGGAATGACTG[G/T]GGGGGGGGGGTGAGG | 74589 |
rs51179694 | snp | A/C | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88609611 | AAACCCTTTCCTCCC[A/C]AACTTGCTTCTTGGT | 74589 |
rs51394372 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88624067 | ATAAATATATGATGA[A/T]TTTGGTAGAGTGTAT | 74589 |
rs51478779 | snp | A/G | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88625517 | CTGCCTCTGTCTCCC[A/G]AGTGCTGGGATTAAA | 74589 |
rs51855627 | snp | A/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582318 | CTGGCTTTGTCAACA[A/T]CAGGCAACTAGCTCC | 74589 |
rs51856381 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88613353 | CTGGCCACTGGTCAC[A/T]CAGTGGTCAGAGGGA | 74589 |
rs107654469 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609575 | TGGTGATGAACAGCA[A/G]TGTGGAAACATAAGC | 74589 |
rs108159701 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88555397 | GGGTTTCTGTCCTGA[C/T]TCCATTCAGTGATGA | 74589 |
rs108844174 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609556 | TTCCAGTCCTGACTT[C/T]CTTTGGTGATGAACA | 74589 |
rs211719880 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88584488 | TTTCAGCTCCTAGCA[C/T]CCATGTTGGATCCCG | 74589 |
rs211738161 | in-del | -/GG | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88589808 | GTGGGGAATGACTGT[-/GG]GGGGGGGGGGTGAGG | 74589 |
rs211807818 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88578360 | TTTATGGAGGCCTCC[A/T]TTTGCTAAGTCACAG | 74589 |
rs211816107 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88625539 | GGGATTAAAGGCGTG[G/T]GTCACCACACCTGGC | 74589 |
rs211846421 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88563126 | AAATTCCATGTTTTT[A/G]CATAGTTTTTGGTCA | 74589 |
rs211930698 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88549225 | AGAAAAAAAAAAGTT[C/T]TTTCAGTATAAAAAG | 74589 |
rs211966908 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88597989 | AAAAAAAGTTAGAGC[A/G]AATTTTAACTGAAGG | 74589 |
rs212059714 | in-del | -/AAAAAAAA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88626564 | TTCCCGCATTTATAG[-/AAAAAAAA]AAAAAAAAAATGGCA | 74589 |
rs212086150 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88590034 | ACAAAGAAAGGGAGA[A/G]AGCCAGGGCCTCTGA | 74589 |
rs212136897 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88598555 | TTAATTTTGGATTCT[G/T]GGTCTTCATCTATAG | 74589 |
rs212146993 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88550617 | CTATGCAAAGAAGGC[G/T]CTGCTCTGTGTGAGC | 74589 |
rs212271837 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88584158 | GTTTTGCCTTTTTCG[C/G]CCTCTGCATGAAACA | 74589 |
rs212305772 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88585396 | AACCAGCTCCCCAAA[A/G]TTGCCCTTGGACTTC | 74589 |
rs212353997 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88555653 | GATAACTTAAGCTTG[A/T]GTCAAACTGACATAA | 74589 |
rs212356326 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88616549 | ATAAAACATGTGACA[C/G]CATTGATACTTATTA | 74589 |
rs212359906 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88600808 | TCCCAGCACCCTGGC[G/T]GGCTCACTGTGACTC | 74589 |
rs212393688 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88608721 | GTGTATGTAGCTACC[C/T]TAATACAGACAGTCA | 74589 |
rs212433507 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88599913 | TACTGAGAACCATCA[A/T]GCCTGCCCGGCTTCT | 74589 |
rs212492605 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88550041 | ATCCCCCACAGATGC[A/C]GACAGGACTTAGTTG | 74589 |
rs212532384 | snp | C/T | | | synonymous-codon | Kbtbd12 | Mm_Celera | 6:88618664 | AGTGCACTCGAGTAG[C/T]CCACAGGTGAACATA | 74589 |
rs212539869 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88557470 | CACCCTTGTCCCACT[A/G]TATGGGTTCCAAGTA | 74589 |
rs212564215 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88551418 | GGAGAGAGAGCTTGG[C/T]TTGCTGGTACAACTA | 74589 |
rs212570768 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609797 | GTGCCTTCTATAGTG[A/G]ACTGAAATCCCTCTG | 74589 |
rs212576171 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88557892 | CCCTGAGTCTACATT[C/T]AGATGAAAGTAGGCA | 74589 |
rs212584633 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88563837 | GACAATAGTAAGGTA[C/T]CCTGAGTTCCCCTTG | 74589 |
rs212594762 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88602000 | AATTTTAAAAAGATA[C/G]CCCTAATGGTATTTT | 74589 |
rs212661534 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88610156 | TGGAGAGAGGGCTTC[C/T]GAGATTGCTTCTAGG | 74589 |
rs212678352 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88551882 | TTAAAACTTGTCTTT[C/T]ATCTTTTCCTTTCCT | 74589 |
rs212739496 | in-del | -/A | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88557558 | TATTTAACTAGCTTT[-/A]AAAAATGTTAGCATT | 74589 |
rs212750439 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88585865 | AGGGCTATGCAGAGA[A/T]ACCCTGTCTTGAAAA | 74589 |
rs212766203 | in-del | -/CCTGA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88553384 | CCACCTTCCCTGCAC[-/CCTGA]ACTGGAGCCAAAGCA | 74589 |
rs212775307 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609247 | CTATTTTGAAGGTGG[A/T]GGACCCAGGGTCTGC | 74589 |
rs212803184 | in-del | -/TCT | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88558185 | TGTCACTCTTGGTAC[-/TCT]TCTAAGCTCAGGGCT | 74589 |
rs212920322 | in-del | -/AAC | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88550921 | GTTTTCAGTGCCTGA[-/AAC]AACACCTCAGTCCAG | 74589 |
rs212984560 | snp | A/C | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88629293 | TCACCACTTCCATTT[A/C]TATATTTTAAAATCA | 74589 |
rs213014098 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88575561 | AGAAGAGGGTGTCAG[C/T]GCTTCTGGAGTTGGG | 74589 |
rs213023881 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88602759 | CTGCAGTCATCTATA[G/T]CTATACCTACACGTG | 74589 |
rs213034253 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88621193 | TCTTAGCTGCTGAGG[C/T]ATCTCTCCAGGTAAT | 74589 |
rs213063009 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88549522 | TACATCTGCTATAAA[-/T]CCCTTTTTTTTGTTG | 74589 |
rs213098141 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88591908 | TTCTCTCCTTCCCCC[-/T]CTCCTTTCCCCCTCC | 74589 |
rs213168613 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88594753 | AAAGTCTTGTTACCG[C/T]GAAGCTTGGTACTCT | 74589 |
rs213200334 | snp | A/G | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88627550 | GTGCAAGGGACAGGC[A/G]GCGTCCCAGCGAGGA | 74589 |
rs213212227 | snp | A/G | | | synonymous-codon | Kbtbd12 | Mm_Celera | 6:88586823 | GAGCTTCCCGTCCAC[A/G]GCGCCAGCACTGGTG | 74589 |
rs213249415 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88566331 | TCCCCAGGGAGAGCA[C/T]ACCAGTTGGTCAGCC | 74589 |
rs213288483 | in-del | -/A | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88574056 | TAGTACCAATAAGTT[-/A]AAAAAAAAACTTTTC | 74589 |
rs213289044 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88582030 | AGCAGGACAGTAGAG[A/T]TGATTGCCCTACTTT | 74589 |
rs213343193 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88548344 | TATTGTATCAAGTAC[C/T]GACAGAATACGCGGC | 74589 |
rs213380971 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88597075 | AGAAGGACATGCTTA[G/T]AAAGGTACAAGAAGC | 74589 |
rs213399455 | snp | A/T | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88628840 | TCATATTTTTCCTTT[A/T]AAAAAAATCTTTGTG | 74589 |
rs213431561 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88574613 | CTCCAACCAGGCCAC[C/T]CCCTGGCCACGCATA | 74589 |
rs213454024 | in-del | -/TA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88583071 | ATAATCTGGCTATAC[-/TA]TAATAATAATAATAA | 74589 |
rs213475537 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88559085 | GTGTAGTGCCCACAG[A/G]AGCCAGAAGAGGATG | 74589 |
rs213482240 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88548042 | TTTGAGAGCCAAGGG[-/T]TAATCAACAAACCAA | 74589 |
rs213491539 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88552548 | TGGTTAAATAAAATT[A/G]GCAACCATCAATTAC | 74589 |
rs213502690 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88621945 | CTGACCCCAAAGTCT[A/G]TATCCTTCTTCCTTC | 74589 |
rs213539311 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88612012 | TGTATTTACATATTT[A/T]CTAACTTTATATATT | 74589 |
rs213546157 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88553219 | CTTGTGAGTGAGGGA[A/G]TTCCTACACAGGGCT | 74589 |
rs213611660 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88559525 | CAGAGACCCTCCCAC[C/T]TAAAAGTGACATAGT | 74589 |
rs213619763 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88593902 | CAGACACCATGCATC[C/T]GGTTTCTGTGTTTTG | 74589 |
rs213649728 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88553739 | CTCACAGATGTGTGC[A/C]AACTGTGCAAATAGT | 74589 |
rs213649816 | snp | C/T | | | downstream-variant-500B | Kbtbd12 | Mm_Celera | 6:88547640 | CACACTATGCCTATG[C/T]CCTGCTTTGCATTCT | 74589 |
rs213649880 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88590213 | TTACATACACAAGTG[-/T]TTTTTGGAAATTGTT | 74589 |
rs213655291 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88606004 | ATGTTGAATCAGAAA[A/G]CCCGCATGATGTTAT | 74589 |
rs213689550 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88613833 | TCTTTACTACTCAAT[A/G]ACTGCTACATTTTTC | 74589 |
rs213730365 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88615243 | AATTGCAATTTGAGA[C/T]ATTCGGTAGGAGAAA | 74589 |
rs213730386 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88607310 | CTCCTACAATACATG[C/T]TTGCATTTCTTGACT | 74589 |
rs213738371 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88549376 | TGCCACTGGTGTGGG[A/G]ATTCTTAGAGTCCAG | 74589 |
rs213763569 | in-del | -/GCTGG | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88615776 | ATCATATGTCTATAT[-/GCTGG]GCTGGTGTCTCTTAA | 74589 |
rs213844665 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88549625 | GAAGGGCATCCTGGT[A/G]GTCATGTGTTCCTCC | 74589 |
rs213891928 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88584073 | TGGATGGGAGGGATG[C/T]AGGCAGGAAATATGT | 74589 |
rs213989618 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88589276 | AGGGTGGGATCGGCA[G/T]AGCTGCAGAATGTCA | 74589 |
rs214065563 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88602094 | CATTGCTTGGGTGGC[-/T]TAGTTTGGAATGTGG | 74589 |
rs214067643 | snp | C/G/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88598655 | TGGAGGAAGAGTACT[C/G/T]GAGGGAGAGTAAGTA | 74589 |
rs214077512 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88579149 | GTGGAAGTCTGCAAC[A/T]GGCCCTGATGCAGCT | 74589 |
rs214157234 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88580022 | TATTGAAAGTAACCA[C/T]GTAATGTGTGGCCCA | 74589 |
rs214169083 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88604985 | CCAACAAAATAAAAT[A/G]AGGGCCAATATTCAA | 74589 |
rs214215677 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88596419 | TGCCCAAATGTCAGC[A/G]TAAGAACATAATCAA | 74589 |
rs214242356 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88624745 | ATATTTGGTACAGGA[C/T]TGGAGACATGGCTAA | 74589 |
rs214260022 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88625441 | AGGGTTTCTCTGTAC[A/T]GCCCTGGCTGTCCTG | 74589 |
rs214325202 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88555395 | ATTCATCATTGAAGG[A/G]AGTCAGGACAGGAAC | 74589 |
rs214337417 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88584560 | TCAGCTTGGTGCACA[A/G]CAGCTGATTTTCTGG | 74589 |
rs214419217 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88584918 | TCTGTTTGTCTCTAA[C/T]GTCACAGTGATGTGC | 74589 |
rs214580440 | in-del | -/TTAAG | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88588399 | GCATGAACCCAGAGA[-/TTAAG]ATATCTACGCAGGAT | 74589 |
rs214604830 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88560740 | CAGAGCGGCTGTTTT[A/G]CTTGGCATTCTCACC | 74589 |
rs214613864 | in-del | -/GTGTGT | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88559039 | TCTCTCTCTCTGGGA[-/GTGTGT]GTGTGTGTGTGTGTG | 74589 |
rs214646912 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88590068 | CTCGTGGGTATCACC[A/G]AGGGAACTTTCTTTT | 74589 |
rs214652206 | in-del | -/CACACACACA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88603990 | CTACAGGCATGCATG[-/CACACACACA]CACACACACACAACA | 74589 |
rs214679422 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609422 | GTGGGTGGTGCCATC[C/T]CTGGGCTGGTAGTCT | 74589 |
rs214681073 | in-del | -/CCTGAGAC | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88579725 | GGTTTCACTTAATTG[-/CCTGAGAC]AATTATATGAACTTT | 74589 |
rs214689352 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88550835 | GTGTGTGGCACTGTG[A/G]CCTCATGGCAGTCCT | 74589 |
rs214715274 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88600844 | TTAGGGGATCTGATG[C/G]CGTCTTCTGCCTTCT | 74589 |
rs214722339 | in-del | -/GTA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88582589 | AATCAGCTGTAGACT[-/GTA]GTAAACTGCTGAGCT | 74589 |
rs214757951 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609664 | AAACCCTGACTAAGA[C/T]ACTGGCTAAAGTAGG | 74589 |
rs214794817 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88601539 | TATCATGACTGCTCT[C/T]TGAAAAGCCCAACAA | 74589 |
rs214805691 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88551314 | TTGCCGCTTCCAAGC[A/G]CTCGGACTGACTGGA | 74589 |
rs214867742 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88626647 | CACATCTGCCCACCC[A/G]TGCTAAGCCCTAAGT | 74589 |
rs214886881 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88564862 | TCAGGCTCTGGGTGG[A/G]ATCTAGGCATCCAGG | 74589 |
rs214897459 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88602801 | ACACGCACACGCACA[C/T]GCACACTCACACACA | 74589 |
rs214914496 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88626256 | AATCTTGCCTGCCTC[-/T]TGTCTCCTGTGTGCT | 74589 |
rs214932601 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88603433 | TACAATAAGCTAATT[A/C]TTTTTATTTTTTATA | 74589 |
rs215012773 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88599325 | CATGTATGGTTTGTA[C/G]AGATACATGGCTGTC | 74589 |
rs215053961 | snp | C/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88581302 | ATATGTTTTATTTAG[C/T]CTCCTGTATATATTT | 74589 |
rs215056093 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88566365 | CAAACATCCACACAA[A/G]TAACAGTGACCAGCG | 74589 |
rs215060955 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88590639 | CTTGGAGAAAAAGTA[A/G]CCCACCGCTCTGAGT | 74589 |
rs215083283 | in-del | -/TTTT | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88582391 | AAAAATTAGGTCTAG[-/TTTT]TTTTTTTTTTTTTCC | 74589 |
rs215085621 | in-del | -/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88598013 | CTGAAGGGCAAATTC[-/G]ATTTTTTTTTTTTAC | 74589 |
rs215140085 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88567128 | CTTTTTCCCTCCCCT[A/G]TTCTTTTCAGATTCT | 74589 |
rs215191896 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88610230 | GCATCCAGCCTAGAT[A/G]AGGTTCCTTGTAAGG | 74589 |
rs215225935 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88592232 | ACTACCTAACAGGAT[A/T]CAGACCAAACTCCTA | 74589 |
rs215244871 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88575652 | TTACAAGAGCAGTGC[A/G]TGTCTTTAACCCTGG | 74589 |
rs215263359 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88592688 | CAACTCCTGAAAGTT[G/T]TCTTCCACATGTGTG | 74589 |
rs215283183 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88613713 | TCTAGAAGCAACACA[-/T]TTTTTTTAAAAAAAG | 74589 |
rs215298505 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88558550 | ATACACCCCATGCTT[C/T]TTAGGGCGTGCTCTG | 74589 |
rs215313022 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88586123 | CTCTGGGGCGTGTGT[C/G]TCACAGGTATATATT | 74589 |
rs215315838 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88552308 | TGATTGTGAGCTGCT[C/T]TGTGGAACTCAAACC | 74589 |
rs215324723 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88576238 | GTACTAGAGAGAAAT[A/C]CTGGGCTTAGGAATC | 74589 |
rs215402427 | in-del | -/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88573516 | TTTAGAAAAAAAAAA[-/C]CCACAAAAATACAAA | 74589 |
rs215447729 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88593449 | TTTCCCAGTTGACAG[-/T]TTTTTTTTTTTAACA | 74589 |
rs215490568 | snp | C/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88556831 | TGACAGAGTCCTTTG[C/T]GCCAAGTTGAAAACT | 74589 |
rs215493693 | snp | A/G | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88627803 | ACACCTTTGAAAAGA[A/G]AATTTGGAAATCGGA | 74589 |
rs215506529 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88582355 | CCAGGCTGCAGCTAT[A/G]TTGTTAGCTCATTTC | 74589 |
rs215538677 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88582626 | TTACTGAAAGCCAAG[A/G]CAAACCAGTCCAGCC | 74589 |
rs215654699 | in-del | -/GTACGTGTGTAC | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88612991 | TGTGTGTGTGTGTGT[-/GTACGTGTGTAC]GTGTGTACGTGTGTA | 74589 |
rs215706980 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88552057 | CTATCCTGGAACCCG[A/C]TATGCAGACCAGGCT | 74589 |
rs215739180 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88621048 | GTGCACTGTGTCTGC[C/G]TCTGCGGTACCTACA | 74589 |
rs215821331 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88548357 | ACCGACAGAATACGC[A/G]GCTGTTGTCAGGGTG | 74589 |
rs215839544 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88607054 | GTTCAATTCCCAGCA[A/C]CCACATGGCAGCTCA | 74589 |
rs215842353 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88597154 | ATAATGATCAAAGTA[C/T]TAAATTCACAGAACA | 74589 |
rs215860906 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88584635 | TTCTGCGATCTACTA[-/T]TTCTTGGTTTACATA | 74589 |
rs215927333 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88597837 | GAAATATATCTATGT[A/G]AAACCAATATACCTG | 74589 |
rs215930270 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88622915 | TAGCTCTCAAATTGA[C/T]AATAGGTTGATTTTA | 74589 |
rs215946771 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88595280 | TCTGGGGTTCAGGAT[A/G]CAGTGACATATGGGA | 74589 |
rs215965053 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88612718 | ATCCAAAGAGCAAGC[G/T]AGAGTTATCTGTACC | 74589 |
rs216012094 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88598803 | TATTATCTCAGAGTC[A/G]CTTAAAATACATATT | 74589 |
rs216029542 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88596123 | AGACTATTTAGATTA[C/G]TTTATGCTTTCTAGG | 74589 |
rs216030933 | snp | C/T | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88628340 | GCTTTAGTGTAGTAA[C/T]ACACATTTGTGTGAG | 74589 |
rs216046995 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88599427 | GGATGATGGCAGCAA[A/G]GACTGAGGACTCAGG | 74589 |
rs216096565 | in-del | -/GA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88548829 | TATCTATATGTGTGT[-/GA]GAGTGAGACACATGT | 74589 |
rs216130952 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88587992 | TGCCTCTCTTTCTCA[C/T]TGCTACTTAGACTCT | 74589 |
rs216132505 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88590680 | CCTTCTGACTCACGA[C/T]CTGAGCCTCTGCCTA | 74589 |
rs216136342 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88619955 | CAGTGAGAAATGGTA[A/G]CGAGTCCCCAAATTT | 74589 |
rs216157274 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88557983 | TTAAATACATGTGTG[C/T]TGCCATTGTTCCCAG | 74589 |
rs216177212 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88561874 | CAAAGCAAAACAAAG[C/T]AAATTGAAATAATTT | 74589 |
rs216178747 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88578341 | AAGGAAATAGTAAGA[A/C]TGTTTTATGGAGGCC | 74589 |
rs216195417 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88625485 | AGACCAGGCTGGCCT[C/T]GAACTCAGAAATCTG | 74589 |
rs216209395 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88562946 | TACCAGGATTAGGCT[A/G]CAGTTTTCAAATCCC | 74589 |
rs216266807 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88622061 | CTTATGGCACAAAGG[A/C]AGCCACAGGGAAAGA | 74589 |
rs216269095 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88589321 | TGGCTTTCATTTATG[C/T]GCTACCAGAATCTCT | 74589 |
rs216352222 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88559563 | AACAGTGCCAGCAGC[C/T]GGGGACCAAGTCTTA | 74589 |
rs216369530 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88612071 | ATAATTTTATTCTTA[C/T]AGAGATACAGAGTTT | 74589 |
rs216372835 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88584131 | CCTGATAGGAAATTC[A/G]GTGGCCATGAGGTTT | 74589 |
rs216378053 | snp | A/C | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88627511 | CTGGGCTGACAAGCA[A/C]TATAAATAGACCAAG | 74589 |
rs216406776 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88566132 | TTCCCTGCCCCCACC[C/T]TGAGCTGAGGACTGA | 74589 |
rs216408823 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88556867 | TGAGAGTTTCTCTGG[C/T]GCTCTTCGGAGCTCC | 74589 |
rs216435077 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88553271 | TCTAAGCGTGGGCAG[C/T]ACCATCCCATGGGAA | 74589 |
rs216476924 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88553834 | TTCCCCAAGGATGCC[A/G]TCAGAGAAATAAGAT | 74589 |
rs216486672 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88587581 | AGTGAAGGCAGAACA[C/T]GGTGGCACATGACTT | 74589 |
rs216541254 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88592141 | AGCAGACCGTGTTCC[A/G]CAGAGACTGTAGCTG | 74589 |
rs216587713 | in-del | -/T | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88628953 | TATATAAACTATAAC[-/T]TACTATAGTTTGGAT | 74589 |
rs216816632 | snp | C/T | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88628448 | ACATGAGAGTCTGTA[C/T]TAAAGGGTCACAGCA | 74589 |
rs216834612 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88573516 | TTTAGAAAAAAAAAA[A/C]CCACAAAAATACAAA | 74589 |
rs216877105 | in-del | -/AAACAAAC | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88624909 | ATGTATAAGTATAAT[-/AAACAAAC]AAACAAACAAACAAA | 74589 |
rs216906261 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88584412 | AAAAGCATTGTGAGT[C/T]AGGGGCTGGGGAGAT | 74589 |
rs216928439 | in-del | -/TTTTT | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88620458 | ACAAAAAACCCTATG[-/TTTTT]GTTTATGTTTGTTTG | 74589 |
rs216940483 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88601870 | GTCTGGTGGGGTGGG[A/G]GTGGGGGGACATCTT | 74589 |
rs216973136 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88592826 | ATTTTTAATATATTT[A/G]TTTTGTTTTATATAT | 74589 |
rs216973180 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88602483 | AAACTTCACCCCAGG[C/T]CTCTCAGGACACAGG | 74589 |
rs217044225 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88593788 | GTGATAGGAACGAAA[C/T]TCTAGTGTTCTTAAC | 74589 |
rs217110363 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88595368 | TCACTTTATACATTC[C/T]GTGATGTTGAAGTGG | 74589 |
rs217137404 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88596357 | TCCATTCAACAAAGA[C/T]AAACCCAGAAATTGG | 74589 |
rs217171368 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88549141 | ATTTTTACACAATTA[C/T]CTTATGACTAAAATG | 74589 |
rs217196156 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88588516 | AGAAAGGGTCACATC[A/G]GCCTTAGCACAGTTC | 74589 |
rs217213217 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88558908 | GGAATAGTATTACTA[-/T]TTAATTTTTTTTTAG | 74589 |
rs217225717 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88574381 | AGGAACAAGGCAACT[C/T]TTATAAAGGACAACA | 74589 |
rs217244727 | in-del | -/ATAT | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88599660 | GATATCTCCCCCTCC[-/ATAT]ATATATATATGTGTA | 74589 |
rs217253867 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88558729 | AGAACTCAGAAATCC[A/G]CCTGCCTTTGCCTCC | 74589 |
rs217270242 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88550014 | ACTCAAGAGATTGGG[C/T]TCCCACTAGAGATCC | 74589 |
rs217272826 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88608659 | AGAGAGTGATGAGAG[A/G]CCTTATAAGGTTCAT | 74589 |
rs217273142 | snp | C/T | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88628812 | TCTCAGGTTGGATCA[C/T]TCTGGTGCACACTCA | 74589 |
rs217282949 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88615323 | AGAAAAATATAGAAA[A/C]GTTTATGTGAAACAT | 74589 |
rs217295371 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88621146 | TAGATGTTAGAAATA[A/G]AACCTGGATCCTTTG | 74589 |
rs217314244 | in-del | -/AATA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88623923 | TATAATGGAAAAATG[-/AATA]AATGTGATCTACATG | 74589 |
rs217336179 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88555519 | CTTTCTTATAGAACT[C/T]GGAACCACCAGCTCA | 74589 |
rs217345800 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88623082 | AGAATCTGACTCCGT[A/G]TCTACTGTAATGAAG | 74589 |
rs217357040 | in-del | -/TA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88573654 | AACTTTAAATCATCT[-/TA]TACTAAACTGACTAC | 74589 |
rs217360319 | in-del | -/AAAAAAA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88577809 | GGCCTCCGTGAGATT[-/AAAAAAA]AAAAAAAAAAAAAAA | 74589 |
rs217360339 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88608243 | TCCAGTAAAGCCCTG[A/C]AACACCACAGTCTAA | 74589 |
rs217431639 | in-del | -/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609209 | GTCTCCAAAGGCTCA[-/C]AGTTGGTCTCCAGCC | 74589 |
rs217438000 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88613782 | AAGTTTATAGTGTAT[A/G]GGGTTAAAAGCATGT | 74589 |
rs217481425 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88560466 | GTTGGTGTGCTCGCT[A/G]CACTGTTGAGTTCTA | 74589 |
rs217515054 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88553928 | ACTATTTTGGGGGTC[A/C]CACAGATGGGGGCTG | 74589 |
rs217515150 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88561641 | AAGGGAGGTTGAAGC[A/C]TTTAAGAACACTTAT | 74589 |
rs217544529 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88617400 | TAGCACCGCCTAAAT[G/T]CAGCCAAACAAAAAC | 74589 |
rs217598807 | in-del | -/CTAACC | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88553578 | CTCTTAATTCACACT[-/CTAACC]CTTAATAACAGACAA | 74589 |
rs217612925 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88554278 | TCTGTATTCCTGATC[C/T]ACAATTTCTGTCTCA | 74589 |
rs217616477 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88616228 | ATCTTAGGGAGACAG[A/C]ACTCTCTCAGGGCTT | 74589 |
rs217652605 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88573866 | GAGAGCACTTTGCAC[-/T]TTTTCAATGTACAAG | 74589 |
rs217663851 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88561177 | GTCTTATGAGAGGAT[G/T]TTTTGCTGAGGCAGG | 74589 |
rs217672305 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609494 | AGCCAGTAAGTAACA[C/T]CCCTCAATGGCCTCT | 74589 |
rs217733690 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88550968 | ACTGTGTGTTAGGAA[C/G]TGTAGGTTTGAAGTG | 74589 |
rs217797950 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88584959 | CCTCTTTTATCTGCT[C/T]CCCAGGGCATTTGGT | 74589 |
rs217813677 | in-del | -/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88625639 | ATACCCTCCTTCCCC[-/G]GGTCCAGTTCTTCAG | 74589 |
rs217818229 | snp | C/G | | | synonymous-codon | Kbtbd12 | Mm_Celera | 6:88618370 | ATGAAGGCTTACCTC[C/G]GCGAAGTGCTGGTAT | 74589 |
rs217825210 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88624038 | ATAAAGTATAGGTCA[C/T]ATATTATGATGACAT | 74589 |
rs217858580 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609775 | TTCCACCACAGACCA[C/T]CATCACGTGCCTTCT | 74589 |
rs217866225 | in-del | -/CCAGTTCTAATGTTT | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88625344 | TCAGAAAATAATGTC[-/CCAGTTCTAATGTTT]CCAGTTCCAAAGCGA | 74589 |
rs217897405 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88624970 | ACAGTAAATAGGTTA[C/T]AATTATGGTAAAAAT | 74589 |
rs217903544 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88613065 | TGCATATGCAAACCA[G/T]ATGTTAAGCCCAAGT | 74589 |
rs217925793 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88579362 | GCTCAACTGAATAAA[C/T]GAGCTTACTGCGTTC | 74589 |
rs217938389 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88614562 | TAATTTACTTTAGTA[A/C]AATATGGAAGAAATC | 74589 |
rs218040377 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88585369 | GTGCCAGTCCCCAGG[A/T]CCCACATAGACAACC | 74589 |
rs218046238 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88584771 | GTCAAACTGCGCAGG[C/T]TGACAATGGTTCTCT | 74589 |
rs218066483 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88588648 | GGTTTGTGTGTGGCA[G/T]CAGAGACCTGCAAGG | 74589 |
rs218074573 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88585048 | GACACACCCCGTCCA[C/T]TTTCTCTGTTCTTTT | 74589 |
rs218081943 | in-del | -/CTATGA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88616012 | CACTTGCATGGACAT[-/CTATGA]ACCATGCAACCTAGG | 74589 |
rs218084006 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88580079 | AGATAGATTATATTA[G/T]GATGAATTTTTAAGT | 74589 |
rs218129528 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88625744 | GATACCTGGTATGGA[A/C]GAGTTGCTTGGTCTC | 74589 |
rs218250993 | in-del | -/CTCTCCAGCATCCATCCACCCTGCTCCTTCAGCAGGAACT/GCAGGAACTCTCTCCCCCATCCATCCACCCTGCTCCTTCA | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88585222 | CCTAAATCTTAATTC[lengthTooLong]GCAGGAACTCTCTCC | 74589 |
rs218288451 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88581933 | ATTGGGCACAACAAC[A/G]ACTCTATCTGGATTG | 74589 |
rs218289431 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88589709 | TTCTACTCTGATCTG[A/G]GCTTGATCCAAAGCA | 74589 |
rs218322204 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88590297 | AGGGTCAAATGCTCA[G/T]AGACATTTCTTTTGA | 74589 |
rs218335143 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88595646 | TTAAAATTTTGATCG[-/T]TTTTTTTTTTCTCCT | 74589 |
rs218384951 | in-del | -/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609567 | CTTTCTTTGGTGATG[-/G]ACAGCAATGTGGAAA | 74589 |
rs218445808 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88551333 | GGACTGACTGGATGC[A/G]TGTGCTGAGGCAGGG | 74589 |
rs218507189 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88626227 | GGTAGCCTTAGCTGG[C/T]CTCTGATTCACAGCA | 74589 |
rs218537469 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88551075 | TCCTGAAGTGGACAC[A/G]GGTGAAAGACTAAGG | 74589 |
rs218589906 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88616912 | GCCATGACTGTGCAA[A/G]AGAGACAGAAAAGGC | 74589 |
rs218622952 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88617494 | ATGCTATATTGATAT[C/T]GTACATATATAATAT | 74589 |
rs218652001 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88586168 | TTGGTGAGGTCAGAA[C/T]CAGCTAGTTAGTCTA | 74589 |
rs218656267 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88592488 | CCAAGTTTGCACACA[A/G]GATGACCTCAGTTTG | 74589 |
rs218695772 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88585723 | AACCCATTAAGTCTC[C/T]TCTAATTCACAAAGA | 74589 |
rs218716347 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88557674 | ATGGAGTATGGGTGC[A/G]GCAGGAGGGAGCCTT | 74589 |
rs218723678 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88553158 | GTGGTGGTTAATATC[A/G]TCAGCCTGACAGGAT | 74589 |
rs218740082 | snp | A/G | | | downstream-variant-500B | Kbtbd12 | Mm_Celera | 6:88547595 | CTTTGCACAGGGTCT[A/G]CTATGCATGCGATAA | 74589 |
rs218743124 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88604914 | CCTGAGGTACTAACA[A/G]AAGACCAAAACAGAC | 74589 |
rs218761012 | in-del | -/TAAA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88551819 | CTTAAGAACCATCAT[-/TAAA]TATAGGATTTGAAAA | 74589 |
rs218798865 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88551719 | AGTTGCTCCAAAGAA[A/C]CTTTCTAATCAAGTA | 74589 |
rs218815438 | in-del | -/TTT | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88612352 | CAGTGAGACTGACTC[-/TTT]AGAGACTACAAAGTA | 74589 |
rs218857974 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88552134 | GACATTAAAGGCATG[C/T]ATCACCATACACAGA | 74589 |
rs218880792 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88550309 | AGTATGTGTGGCTTC[C/T]ACTGAAAGAGCCTAA | 74589 |
rs218892739 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88619239 | TAAAAAGATAAACAC[A/G]TTTTGCAATTCCATT | 74589 |
rs218916930 | in-del | -/TTA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88555580 | TCCCACACCAGTCAC[-/TTA]TTAAGGAAATGCCAG | 74589 |
rs218972538 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88620478 | ATGTTTGTTTGTTTT[G/T]GTTTGTTTTGGTTCA | 74589 |
rs218973692 | snp | A/C | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88595816 | AAACAAAAAACCCCC[A/C]AAAAAACAAAAGACC | 74589 |
rs218997058 | in-del | -/GAA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88559871 | CAAACCCTGACTCAG[-/GAA]GAAGGAGGGGGAAGA | 74589 |
rs219004907 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88610483 | CTCCGTTAGAGGCCT[A/G]GTTTGCTTTTACTCA | 74589 |
rs219085291 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88603665 | CCTGAGGCCAGTGCT[A/G]TACTCAGCGAGGAGG | 74589 |
rs219095538 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88552424 | TTTGGTCTATTGTTA[C/T]GTATTGTAATGCTAC | 74589 |
rs219126676 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88586248 | TGGCCTCTAGATTCA[C/T]GCATGCTTAAAAGCC | 74589 |
rs219180836 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88625869 | GTTGCTGTATCTCAG[-/T]TACGTTCTTCTAGCT | 74589 |
rs219283374 | in-del | -/CTTA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88581023 | TTTACGAGTGAATGT[-/CTTA]CTAACTCTGTTAAGC | 74589 |
rs219291156 | snp | C/G | | | downstream-variant-500B | Kbtbd12 | Mm_Celera | 6:88547283 | TCCTGTGTGTAAGCT[C/G]TGTGGCAGGCTGGAC | 74589 |
rs219302666 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88606191 | ATTTTTTGGTCTTAT[C/T]GTTTGAGACTGTCTT | 74589 |
rs219352602 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88587169 | GCAAGATTTATTCCT[C/T]GCAGACCCTGCAAAG | 74589 |
rs219412335 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88582642 | CAAACCAGTCCAGCC[A/G]ATGTGATTGTGCCCT | 74589 |
rs219415205 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88606409 | TTATCTACCTACACC[A/G]AAAACTGTAAAATAT | 74589 |
rs219513849 | in-del | -/TTTACTTTGTGTCTAAGTAAAATGATCTC | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88593042 | AAGAATCTTGGTCTA[lengthTooLong]TATAGAGTAGTCCTT | 74589 |
rs219520759 | snp | A/C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88607157 | GACAAAAAATAAAAA[A/C/T]AAATTTCATATTAAA | 74589 |
rs219537484 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88575705 | CTGAACATACCGATT[C/T]AGCCAGACTGGCTGG | 74589 |
rs219592362 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88548544 | GTCACAGATGCCACA[C/G]TGTTCCTTAAGGATG | 74589 |
rs219675078 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88577501 | ACATGGTTTTGCTCC[C/G]CTAAAGTTTGTTTGT | 74589 |
rs219686925 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88605523 | TCAGAGGGCAGAATA[A/C]GTGCTGTACAAATCC | 74589 |
rs219744489 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88583863 | GACTGAAGGAAGGAC[C/T]ATCCAGAGACTGCCC | 74589 |
rs219766021 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88576384 | CGGTGCAGAAGAAAT[A/G]AGGACCCCACGAGAC | 74589 |
rs219851491 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88549458 | AAAAATGGAACTATT[C/T]AATTTCCAAGCATTT | 74589 |
rs219870697 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88553502 | CGAGCAAGATTGCAT[C/T]CTTCATGCAAAACCA | 74589 |
rs219895956 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88553981 | TGCTGTATAGAACAC[A/G]TATGATGCAGGTGGT | 74589 |
rs219919696 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88548037 | TCCTCTTTGAGAGCC[A/G]AGGGTTAATCAACAA | 74589 |
rs219943925 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88614801 | CACCTTGCCTGGTTG[C/T]TATTTAAGTTGTAGT | 74589 |
rs219976022 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88607724 | ACCCTAGTGATAACA[A/G]TGGTCCTCTGTCCTC | 74589 |
rs219977569 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88615701 | GAAGCCAGAGATCCT[A/G]GAATTGCAAAGAGTA | 74589 |
rs220006100 | in-del | -/AG | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88583223 | CTGATGTCAACCATC[-/AG]AGTCTTTGAACCTTC | 74589 |
rs220060607 | in-del | -/A | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88565938 | AGCAGCTTCACATGT[-/A]AAGCCCTCACAGCAG | 74589 |
rs220071761 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88579564 | TTCTTTTTTTATGCT[C/G]TTCTGCCTTATTGAA | 74589 |
rs220098213 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88608877 | TCACTACAAAGCTTA[C/T]ATATGAGCTTAAATT | 74589 |
rs220186190 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88576924 | CAGAGGCAGGGTCCC[C/T]GAAAATTCAAGGCCA | 74589 |
rs220221665 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88577571 | GAAATATGTCAAGAC[A/G]TACGCTTCTTCCTGA | 74589 |
rs220228932 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88565455 | ACTACCATTGTCCTG[C/T]TTTGGTGGTCTGCTT | 74589 |
rs220232659 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88550066 | TAGTTGACAACAGAA[A/G]ACCTGAGACCACCAG | 74589 |
rs220316093 | snp | C/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88583673 | AAACTCTAGAACGTT[C/T]GAGGAGGGGATCATG | 74589 |
rs220322586 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88584804 | AGAGCTTCTGAATAC[A/G]CTTGCTCCGCTTCCC | 74589 |
rs220369023 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88579413 | TACTGCTTCGGCTGC[C/T]ACCAGCTGCCAGCCA | 74589 |
rs220406389 | snp | A/C | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88585219 | CTGGCCTAAATCTTA[A/C]TTCGCAGGAACTCTC | 74589 |
rs220436474 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88608272 | AATGATGTAATCTCT[C/T]CCCACTAGGACTCAT | 74589 |
rs220443322 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88576861 | CTCTGACTAGTGCCC[C/T]GGAGTACTTGACTGC | 74589 |
rs220447463 | snp | A/C/G | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88549770 | TTTAACCTGGAGGGG[A/C/G]TGAGTCGAGTCATGT | 74589 |
rs220499640 | in-del | -/A | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88580139 | ATGAAAGATAGATTT[-/A]AAAAACAGTGTTTGC | 74589 |
rs220500055 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88550026 | GGCTCCCACTAGAGA[-/T]TCCCCCACAGATGCA | 74589 |
rs220549270 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88598864 | ACTTAACCATCACCC[C/T]TACCCCAGTGCCAAG | 74589 |
rs220559178 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88599966 | TCTTCAAACTTATCA[A/G]TAAGCACTTTATCCA | 74589 |
rs220575575 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88578649 | CCTGGCACCTGGGTG[C/T]CTGTCAGCAGGGTTC | 74589 |
rs220657370 | in-del | -/TG | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88599696 | GTACATATATGTTTA[-/TG]TGTGTGTGTGGTGTG | 74589 |
rs220681237 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88601050 | AGTCTCAGAAAAAAA[A/C]CACATCATGGGGTTG | 74589 |
rs220689897 | snp | A/G | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88582151 | CTGGTACCTCTGCCC[A/G]CAAAGCGAAGCCATG | 74589 |
rs220714934 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88563279 | CTCCTCATGGAGAGG[A/G]AGATGGGGATATTTT | 74589 |
rs220722526 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609823 | CTCTGAAACAATGAG[C/T]CTCAGTAAACCACGA | 74589 |
rs220724691 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88601132 | CGGATGCATGCCCAC[C/T]AGGGAGTGATACAAT | 74589 |
rs220728901 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88549420 | AGGTGTTGAGCTACA[A/C]TCCCACCATGAATAC | 74589 |
rs220750587 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88607686 | CTGGGTATTCTGATC[A/T]CAATGCTCTGGGGCT | 74589 |
rs220757141 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88602118 | AATGTGGTATAGAGA[C/T]ATTTACACCAATGCT | 74589 |
rs220798612 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88598268 | TTGACAAATGCCCCA[A/G]CACAGGGATGCCCTC | 74589 |
rs220845648 | in-del | -/GC | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88559297 | CAGTTTCTGTTCTGT[-/GC]CATTGTTGTCATCGA | 74589 |
rs220852333 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88581059 | TAGCTCCTTTGATAA[A/G]CTGAGTCATATAAGG | 74589 |
rs220894761 | snp | A/G | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88564360 | TTGGGGCCAGACTCT[A/G]TATGTGACTCTGAAT | 74589 |
rs220976780 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88551169 | GCACGTGAAAGGATA[C/T]GTGATGAAGGATTCT | 74589 |
rs220987062 | in-del | -/A | | | downstream-variant-500B | Kbtbd12 | Mm_Celera | 6:88547374 | CCCAACCTCATCATC[-/A]AAAAAAGCACCCATG | 74589 |
rs221016828 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88600159 | AAGGGTGTGTATACA[A/T]GAGTGCAGTGTCAAT | 74589 |
rs221046620 | snp | C/G/T | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88628512 | GAAGCTGTCAGTGGA[C/G/T]GTGTATTTCTAGGAG | 74589 |
rs221077159 | snp | A/G | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88628901 | CTAGTCATTTTAAGT[A/G]TTCAATCTAGCATCA | 74589 |
rs221152644 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88575967 | AAACATGCTGGCTTC[C/T]TCAACCTATGTTAGG | 74589 |
rs221154702 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88604047 | TTTTTAGAGAGAGAA[A/G]ACAGATGAGAAATGG | 74589 |
rs221184412 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88595626 | TTTTCTTTGAGAATT[G/T]TTCTATTAAAATTTT | 74589 |
rs221187498 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88605114 | TACGGTATCCAACAT[A/G]AGGAAAGGCACGCAC | 74589 |
rs221198136 | in-del | -/CCAT | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88583932 | ACACTATTGTGGATG[-/CCAT]CCAACAAAATTTTGC | 74589 |
rs221216648 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88575838 | GCCTCTGAGCTTTGA[-/T]TTTTTTTTTTTTAAA | 74589 |
rs221236430 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88582042 | GAGTTGATTGCCCTA[C/T]TTTGCTTAGACAAAG | 74589 |
rs221241940 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88592993 | CTCCAGCTTGAATAT[A/T]TTTGTTTAAAAAAAA | 74589 |
rs221272383 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88561062 | CTTGGGGGCAAGTTC[C/T]ACTGAGCTATCCAAT | 74589 |
rs221316486 | snp | A/G | | | synonymous-codon | Kbtbd12 | Mm_Celera | 6:88547764 | TTCCTCGATCAGATC[A/G]GAGGGTGGTGGGATG | 74589 |
rs221333535 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88573738 | TACAGTGTTTTCACT[A/G]TGTACACTTATGTAC | 74589 |
rs221383418 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88574908 | TTTGGGGTGTCTACG[A/T]GTGCTGTCTGTACGG | 74589 |
rs221392693 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88580396 | GAGCTTGGTTTTGCC[G/T]TGTATAGATTGTGGG | 74589 |
rs221440491 | in-del | -/GTTG | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88580430 | TGGGTTGTTTGTTTG[-/GTTG]GTTGGTTTTGGTTTT | 74589 |
rs221448525 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609041 | ACTTCTGGCTTCTCC[C/T]GGCCTTTGCTCTGTT | 74589 |
rs221489954 | in-del | -/AC | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88548282 | TGTACATACAAGTAG[-/AC]ACTCATAATACACAT | 74589 |
rs221578631 | snp | A/C | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88627950 | ATCCAGTTAAATATA[A/C]AATTCAGACATACAA | 74589 |
rs221581110 | snp | A/G | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88628477 | CATTAGGAAGGGTGA[A/G]GATCTCGATAGGTTA | 74589 |
rs221611480 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88566498 | TTAAAAGTTAGCGCG[C/T]TTGGGATAGCATTGG | 74589 |
rs221678033 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88597380 | AGAAAACAAGATATT[C/G]TGTGAAAAAGTTAAA | 74589 |
rs221678199 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88607547 | GCATTTTAGAGGAAC[A/G]GTTTTAAGGCCTTTG | 74589 |
rs221703394 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88598178 | GCCACACAGAGCAGT[A/G]GGTTGTGTAAATGTG | 74589 |
rs221711487 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88596577 | TCCTTCAAGAGGAAA[A/T]AAATGAATCCCTTAA | 74589 |
rs221730049 | in-del | -/TCTG | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88558969 | TCTCTCTTGCATCCA[-/TCTG]TCTGTCTGTCTGTCT | 74589 |
rs221767027 | snp | C/G | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88629076 | TAAGTCCTTAGATTA[C/G]TGGAGGGCATGCCTC | 74589 |
rs221767746 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88558123 | TGTGACCCCAGGTTG[C/T]CACCACCCCCAACAG | 74589 |
rs221787996 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88575345 | CATATGAGTACACTG[C/T]CACTGTCTTCAGACA | 74589 |
rs221805720 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88621444 | AGCAGCAAGACAAAA[C/T]AAATTCAGGGAAGGA | 74589 |
rs221835068 | in-del | -/A | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88604936 | AAAACAGACTGCATC[-/A]AAACAGAAAGCTTCT | 74589 |
rs221874121 | in-del | -/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88607141 | AGGAAAAACAACAAT[-/G]GACAAAAAATAAAAA | 74589 |
rs221887509 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88559320 | TGTCATCGATGTGAC[C/T]GAACACCTGACAAGA | 74589 |
rs221917853 | in-del | -/C | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88628761 | ACTCCGTTACTCCCT[-/C]CCCCCAAAGCTTTGG | 74589 |
rs221920283 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88602881 | TTTATCAAGTCTTAA[A/G]TCTAGACAGCCAGCT | 74589 |
rs221926643 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88626144 | AATGCTTTGTTTAGT[A/T]CTACATCATTCCTAA | 74589 |
rs221968406 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88594432 | CTCAGAGCTAGCTAT[A/G]AGTAGACATACTGGA | 74589 |
rs221994518 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88565807 | GGGCTGTTACAACAC[C/T]GCTGTGTGGACACTC | 74589 |
rs222068353 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88566446 | GGCAGGGAAAATGAT[A/G]CAATTATATTATAAT | 74589 |
rs222068706 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88557166 | CAGGTTCAGTTCCTA[A/G]CAGCAAGTTGGAGGG | 74589 |
rs222087166 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88577590 | GCTTCTTCCTGATTG[A/G]ACCTGATGGGAAATT | 74589 |
rs222098151 | in-del | -/GTGT | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88554893 | TCTTATAAAGTGTGC[-/GTGT]GTGTGTGTGTGTGTG | 74589 |
rs222103598 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88557570 | TTTAAAAAATGTTAG[C/T]ATTGTGGACAGATGT | 74589 |
rs222378200 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88589435 | AAATATATGTCTAGA[A/T]TATTCAGGTGTGGAA | 74589 |
rs222392818 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88575790 | TTACACAGGTTCATA[A/C]AGCAAGCACTTTACT | 74589 |
rs222396426 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88587094 | TTGACTTGTTTTTGC[C/T]GCCTATTTCAAAGAC | 74589 |
rs222422213 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88587696 | GCCAGGGCCACATCA[C/T]GAAACACTGTCTCCA | 74589 |
rs222429620 | in-del | -/TT | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88598014 | GAAGGGCAAATTCGA[-/TT]TTTTTTTTTTTTACA | 74589 |
rs222437464 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88600021 | GTAGTGACATATTTT[A/T]AAAAATTATTTAACT | 74589 |
rs222456750 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88603735 | TTCTTCCTATTTCTA[A/T]GCAGCAGGACACGGG | 74589 |
rs222471718 | snp | C/G/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88591496 | AGTTTAGGAGATGAA[C/G/T]GGTAAAGACCACAAC | 74589 |
rs222471858 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88600892 | TGGTTCAGAAAAGGC[A/G]CAGGAAAAGCACATA | 74589 |
rs222519726 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88578528 | CTTTTTGGGAATTCG[G/T]CCAGTTTTGTTTTGT | 74589 |
rs222544452 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88595522 | TGATTTTAAAACATG[C/G]CTACTTTTTATCTTC | 74589 |
rs222607699 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88563248 | TAAGAATCTTTTTAC[G/T]ATGCAAGTCCCTTTC | 74589 |
rs222640416 | in-del | -/A | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88591046 | CCAAAATCCCAGGGG[-/A]AAAAAGGCAGAAAGA | 74589 |
rs222649918 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88564278 | AAATGATATATTGAT[A/G]TTCAGCCTCCATCTC | 74589 |
rs222653560 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88597358 | AACTTTAAATCACCA[C/T]AGGTGGAGAAAACAA | 74589 |
rs222656215 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88596847 | TAATATAGGACATGG[A/C]AGAGAGAATTTCAGG | 74589 |
rs222658922 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88593364 | TGTAGCAGTATGGCT[A/G]GCCTTCCGTGTGCAT | 74589 |
rs222700215 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88594173 | ACGTACATGCAATGG[C/T]GAACCATTCACCCCA | 74589 |
rs222700989 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88627348 | CGGCCGCTGACCCCA[C/T]ACCGGCCGGCCGACC | 74589 |
rs222723684 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88563217 | TGCAGAACAAATTGC[C/T]ACTTTAAGTGAAGTA | 74589 |
rs222791467 | snp | A/G | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88627908 | TTGAGTACGGCCTAT[A/G]GTAGGGTTGCTGAAG | 74589 |
rs222808716 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88622625 | GACATTAAATGGACA[G/T]ACAAGTACCTATTCC | 74589 |
rs222823487 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88559710 | AGAGGGGAAGGAGCC[A/C]CCTCACTGCCTGTGA | 74589 |
rs222834757 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88555715 | AGGTGGGAGATCATT[A/G]CAGCCCATACATTCA | 74589 |
rs222884611 | in-del | -/TTTAT | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88575303 | TTATTTATTTATTTA[-/TTTAT]TTATTTATTTATATA | 74589 |
rs222929307 | snp | C/T | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88629002 | GTTTGCATGTTGAAC[C/T]GGTGAGTTCCAGAAT | 74589 |
rs222977108 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88592255 | AACTCCTACCGATGC[C/T]TCTACAAAGACCCAT | 74589 |
rs223010061 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88554950 | GTACACATGCATGTG[C/T]ACCTATGTGAATTCC | 74589 |
rs223032814 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88621361 | GTGTCTATAGCAATG[A/G]CATTCAGGTCTTGGC | 74589 |
rs223066208 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88622214 | TTTTAAAAGCTATTT[A/T]AAAACCCGTTCATAG | 74589 |
rs223154326 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88553686 | AACTCAAGGGTGAAA[A/G]GGGCTATAGAGAGTG | 74589 |
rs223165117 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88599025 | AATGGACCTTGGAGC[C/T]CCCTCCCTGAGGACC | 74589 |
rs223178654 | in-del | -/GCCCACC | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88590639 | CTTGGAGAAAAAGTA[-/GCCCACC]GCTCTGAGTCCCCAG | 74589 |
rs223332046 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88627209 | GGCTCCGGGAAGGCA[A/G]GAGAGCCCTTACCTC | 74589 |
rs223343502 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88625130 | GACTGCCAGGGCAGT[A/T]GTACAGAGAAACCCT | 74589 |
rs223400568 | in-del | -/CT | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88557794 | ATGTAACTGCTCCTG[-/CT]CTCTCTGGGACTGTC | 74589 |
rs223444670 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88562247 | TTTGTTTAGCTCTTC[C/T]CAGATACAGATCTTC | 74589 |
rs223448256 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88559433 | TGGGAGTGAACAGTG[G/T]CTTGCTCTGTCATGT | 74589 |
rs223491319 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88553435 | CCTTTGTCAGGCATT[C/T]GATTACAGCTGTCGG | 74589 |
rs223491880 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88553187 | ATCTAGAGTCACCCA[A/G]GAGAAAAGCCATGGG | 74589 |
rs223524083 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88559946 | AAAGAGCAGCAAGCG[C/T]TCTGCAGGCAGAGTG | 74589 |
rs223551133 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88591272 | TTGAAAGTCTCATCC[C/T]GTCAGACTGTAGCAA | 74589 |
rs223574770 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88626274 | TCTCCTGTGTGCTAG[A/G]ATTAAAGGCATGTGT | 74589 |
rs223592568 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88625386 | CGAAATGTTTTATTA[A/G]GAAAGCCTTTTTGTT | 74589 |
rs223620606 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88596759 | GCAATAAATAAAACA[C/G]AAACTGAGGGAATTC | 74589 |
rs223638130 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609720 | CATATCTACCACGGG[-/T]TTCTGTCATTTTTTG | 74589 |
rs223655418 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88615221 | TGGTTTATAAGTGTA[C/T]TTTTCCAATTGCAAT | 74589 |
rs223659213 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88597202 | GCTGTGAGAGAAAAA[A/G]GCCAAGTGACATATA | 74589 |
rs223660049 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88588230 | AGGTCACATGGTTTT[A/G]GTTGAGCCTGCCATA | 74589 |
rs223727467 | in-del | -/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88593331 | TGCCTCTCAAGTACT[-/G]GGGGCACAGGGTTCA | 74589 |
rs223766128 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88559273 | TGTTGTGCTGATTTC[C/T]ACTTTATTCAGTTTC | 74589 |
rs223772211 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88590406 | CTATGGCAGAAGGAC[A/G]GTCCTGAATTTGAAC | 74589 |
rs223798439 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88593106 | ACTTGCTTCTTTATA[C/T]AGGAAACCTCAGATG | 74589 |
rs223844814 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88586339 | ACACACACTAGGCAT[C/T]ATCTTAGAAATGCTT | 74589 |
rs223854959 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88583979 | GGCTTTGCCAATACC[C/T]GGCAAATACAGAAGT | 74589 |
rs223861341 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88552826 | ACATTGGCTGTACTA[C/G]AGAACGGTTTAAGTT | 74589 |
rs223876144 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88612551 | AAACCTGTACTATGT[C/T]TGACCTACAGCACAG | 74589 |
rs224023843 | snp | C/T | | | synonymous-codon | Kbtbd12 | Mm_Celera | 6:88586955 | AACTTGTCCCTTGTC[C/T]CGGCCCACACAGCCA | 74589 |
rs224029774 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88557106 | GGGCTGGAGATGGCT[C/T]AGCAGTTAAGAGTGA | 74589 |
rs224081404 | snp | C/G | | | utr-variant-5-prime | Kbtbd12 | Mm_Celera | 6:88618870 | CCTTGAAATTGGTAA[C/G]TAAGGTTTCTTTGAG | 74589 |
rs224121814 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88621659 | TCTATATTTTCAGAT[A/T]CCGTACTGTCAAGTA | 74589 |
rs224165971 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88557505 | ATTTGGGTTGTCAGT[A/C]TTGGTGACAAGGACA | 74589 |
rs224173376 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88615960 | GGAATGGCCTACAAA[A/G]CTATTTGTCCATTTT | 74589 |
rs224209989 | in-del | -/TAAAAAC | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88607151 | AACAATGACAAAAAA[-/TAAAAAC]AAATTTCATATTAAA | 74589 |
rs224221316 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88551572 | TTGCTAGGTCGTGTC[A/C]CTCACTGCTGCTGCT | 74589 |
rs224246187 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88552219 | ATTTTTATGTGCGTT[A/G]TACACCACGTATGTG | 74589 |
rs224248627 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88610511 | TCAAGAGTTTATCTC[C/T]TTGCTGTCATTTCTT | 74589 |
rs224269803 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88559182 | AAGAGTGGTACCCAC[G/T]ACCGAGCCAAGCCAG | 74589 |
rs224307657 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88552746 | TGACCCCTAGTAGTG[C/T]CAAAGCCAAATAAAT | 74589 |
rs224424550 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88555343 | CCAAAAGCAGGTTGG[A/G]AGGAAGGGTTTGCTT | 74589 |
rs224430249 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88551301 | GTGCTGCAGTCTGTT[A/G]CCGCTTCCAAGCGCT | 74589 |
rs224618306 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88585890 | TGAAAACCAAAAAAA[A/C]CCAAAAAAACCAAAA | 74589 |
rs224635464 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88590613 | AAGATGGTTCTAGAA[A/C]GCCTCAGCTTCTTGG | 74589 |
rs224639142 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88620618 | AGTATTTTATTTGTA[G/T]TGACATGTAAGAATC | 74589 |
rs224660072 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88558273 | ATCACACTAGCAAGG[A/G]AAAGGCACAGGAGGC | 74589 |
rs224666096 | in-del | -/CTT | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88551503 | AGGCACAGCTAAGAA[-/CTT]CTTCTGCTGTTCCTC | 74589 |
rs224675505 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88591745 | TTGACATACTCCTGA[A/T]CCTTTAAGGCCTAGT | 74589 |
rs224677712 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88584839 | CTTCCACCATCACAG[C/T]TCGGAACTCTGACTC | 74589 |
rs224744808 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88623915 | GAATATTGTATAATG[A/G]AAAAATGAATAAATG | 74589 |
rs224752718 | snp | G/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88583476 | AATTTATCTCTGTGG[G/T]TCTTGAGAAATAGCA | 74589 |
rs224758184 | in-del | -/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88595766 | AAACGCCAGAACCAA[-/C]AAAAAAAAAAAAAAA | 74589 |
rs224760106 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88585288 | TGCTTGCATCTCTCT[A/G]ACTTCGACTTCTACT | 74589 |
rs224776189 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88556708 | TTGCCAATCTTGGGA[C/G]CTGGGGAGGCTTTAT | 74589 |
rs224820266 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88550634 | TGCTCTGTGTGAGCA[C/T]GCGTAGTGTTTACCG | 74589 |
rs224827455 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88549596 | TGGTTTCTGGGGCAG[A/G]CTGCCTTTTCTTAGA | 74589 |
rs224844967 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88555904 | TGAGATAATGACCTG[A/G]TCCTTTGTATAACCA | 74589 |
rs224846250 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88622730 | TTGAAATTATGGGAG[C/T]GGGGAAGCCTAGGAG | 74589 |
rs224866593 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88557277 | GAACACACACAGACA[C/T]GCTCGTGAACACACA | 74589 |
rs224934831 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88549958 | GAGCCTCAGTTCCCC[A/C]GGGTGTGGGGTCCAG | 74589 |
rs224975474 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88620979 | GGTATTTAAATTTTT[A/T]AAATTTATTGTTTTT | 74589 |
rs225015316 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88610597 | AGAGGACCCAAACAC[A/G]GTAGCCGTCCAATCA | 74589 |
rs225017093 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609641 | TCATGATGTTTGTGC[A/T]GGAATAGAAACCCTG | 74589 |
rs225044375 | in-del | -/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88558464 | ATACCAAGGAGTAAA[-/G]TGAGATATGGGCATG | 74589 |
rs225061591 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88589513 | CAAAGATGAAGATGG[A/C]CTCTTCTGATGTTGG | 74589 |
rs225062424 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88587867 | TCCAATTGCATAAGA[A/T]TTTCCAATCCACTGT | 74589 |
rs225102567 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88584310 | TTTGGGATTAATAAG[C/T]GACACTGGATATGGA | 74589 |
rs225113519 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88559355 | CTTAAGGAGGAAGGA[-/T]TTTTTTTCCTGAGCT | 74589 |
rs225161924 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88586580 | GGGCTAGATGCGTTA[C/T]AAACTTCATCCCACA | 74589 |
rs225225925 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88554020 | CAGAGATCTGGAGGC[C/T]ACTGACTGCCTGTTG | 74589 |
rs225260324 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88548725 | GCAGTGGAAGTGGAA[C/T]GGGCAGGCTTCCCTC | 74589 |
rs225264480 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88581194 | TCAGAAATTGTTATC[G/T]TTTATTATAAACTGT | 74589 |
rs225301712 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88582168 | AAAGCGAAGCCATGG[A/G]GACCACAGGAGCCTG | 74589 |
rs225313322 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609255 | AAGGTGGTGGACCCA[A/G]GGTCTGCCTGGCTGT | 74589 |
rs225313345 | snp | C/T | | | missense | Kbtbd12 | Mm_Celera | 6:88617975 | CTGGCATCCCCATAG[C/T]TCCTGTGCCTTGATC | 74589 |
rs225367777 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88590093 | TCTTTTATTTAGTTC[C/T]TCTTGTGGATGGCAT | 74589 |
rs225389187 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88549904 | GGAGAATGAAGCGCA[G/T]AAACCGTCCGTAGGA | 74589 |
rs225405010 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88608403 | AACATCAAGAGGCTC[A/G]TGAAAGGCTGTTACA | 74589 |
rs225463406 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88584638 | CTGCGATCTACTATT[C/T]TTGGTTTACATATTC | 74589 |
rs225478018 | in-del | -/A | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88549211 | CACAGGCTTTCTTAG[-/A]AAAAAAAAAAGTTCT | 74589 |
rs225530084 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88614185 | AGGAGAGAGAGAGAG[A/G]GAGAGAGAGATCCAG | 74589 |
rs225539161 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88552293 | AACTAAAGTTACAGA[C/T]GATTGTGAGCTGCTC | 74589 |
rs225566577 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88554707 | GGCACACTGCAGATT[C/T]AAGTAATAGAAAGGA | 74589 |
rs225601988 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88604521 | AAGGAACCTGGCACA[C/T]AGTTTCCTGATTTTA | 74589 |
rs225627885 | in-del | -/CT | | | downstream-variant-500B | Kbtbd12 | Mm_Celera | 6:88547544 | GACCCTGAACCACCC[-/CT]CCCCCCGACCCCGCC | 74589 |
rs225652441 | in-del | -/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88578465 | GGGGAGGATCTGATG[-/C]GGTCTACTCCCCCCT | 74589 |
rs225662649 | in-del | -/A | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88605810 | CACACACACACACAC[-/A]CACACACACACACAC | 74589 |
rs225697084 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88549394 | TCTTAGAGTCCAGGG[C/T]CTCACATGCTAGGTG | 74589 |
rs225720381 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88615746 | TAGTTGTATGGATTT[C/T]TAAAGATGAGGATGA | 74589 |
rs225733372 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88616795 | GAGGAAGGATGCTCC[C/T]TTAGTCTGTGACATG | 74589 |
rs225734482 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88555804 | ATATGATTGTTAATA[G/T]AAGGACAAACACTTT | 74589 |
rs225767040 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88556227 | CAGAAGGACAAACAG[C/T]GGGATGGAGATGGGA | 74589 |
rs225768085 | snp | A/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88548976 | ACTGCTGATACATCT[A/C]TTCATTCTCCTAATA | 74589 |
rs225780855 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88608959 | CAAGACTTACTGGGA[C/T]GGTTATGGATCCAGT | 74589 |
rs225805188 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88580814 | AGATATTTTATTATG[G/T]CCATCTTTATTAATA | 74589 |
rs225809269 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88550173 | AGGCCTCTGGTGTGC[G/T]TGGAACATGGAGATC | 74589 |
rs225883067 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88617694 | ACCCCAGTCTACACA[A/G]AGAGTATTCGGACAG | 74589 |
rs225904627 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88582929 | GCTCAGATTGACCAC[G/T]AGAGAGATTCATTAA | 74589 |
rs225925570 | in-del | -/TTCTGGCA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88610759 | GGACCTACAGGAGAT[-/TTCTGGCA]TTCTTACCATCCATA | 74589 |
rs225992792 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88576189 | TGAGCTCCTAATCTC[C/T]CAGGACCTGAAGTGT | 74589 |
rs226014298 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88552972 | AATTTCATTTAAAAA[A/G]ATCATTAAATGAACT | 74589 |
rs226033846 | in-del | -/AA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88561670 | TTAGAGTAGGTTTTG[-/AA]AAAAAAAATCTAAGC | 74589 |
rs226090074 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88585239 | CAGGAACTCTCTCCC[C/G]CATCCATCCACCCTG | 74589 |
rs226126391 | snp | A/C | | | downstream-variant-500B | Kbtbd12 | Mm_Celera | 6:88547553 | CCACCCCTCCCCCCG[A/C]CCCCGCCCCACCACC | 74589 |
rs226173914 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88587970 | GAAGTTTTTCACATG[A/G]TCTCCTTGCCTCTCT | 74589 |
rs226215511 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88606827 | CCTGCTTGCTCTTCT[C/T]CCACTTTGGTTTTCT | 74589 |
rs226217698 | in-del | -/A | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88612623 | TTATGAGGGGAATGC[-/A]AAAGCATAAGTTTTA | 74589 |
rs226219706 | in-del | -/AAAAT | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88557398 | ATCATAAATTTAAAA[-/AAAAT]AAAATTTACTTATTG | 74589 |
rs226271249 | in-del | -/C | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88559812 | ATGTGACCTGCTCTT[-/C]TGGTGGTAAGTGAAT | 74589 |
rs226373922 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88584370 | TTTATAGCTTCCACT[A/G]CCCCGCTCTCGATGT | 74589 |
rs226403038 | snp | C/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88577884 | GGTAAGCCACCCCAG[C/T]GGTGCGCCACCTTGG | 74589 |
rs226490573 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88582454 | TCCCCCATCTAGCAG[A/G]ACTGTGAGCCTGAGA | 74589 |
rs226514070 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88613611 | GATGCTGCTGTAACT[A/G]CTCCTTGACATGAGG | 74589 |
rs226514412 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88606025 | ATGATGTTATGGCTA[C/T]CAGAGCCGGAGAGGT | 74589 |
rs226575106 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88610415 | TGTCCCATGCTGTGA[A/G]AACAGCCCAAGATAA | 74589 |
rs226587545 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88552093 | CAGACTCTCAGGGTT[A/G]CACCCGCCCTTGTCT | 74589 |
rs226615234 | in-del | -/AAG | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88591198 | AGAAAAAGGAGAAAA[-/AAG]AAAGAAAGAACTCAG | 74589 |
rs226675958 | snp | A/C/T | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88602831 | ACACACGAACACACA[A/C/T]ACAAGTTAACTAGAG | 74589 |
rs226692856 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609112 | AATCGGCTTGCTTCC[A/G]TGTGGTTTCTCAATG | 74589 |
rs226728175 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88600295 | CACTCTTAACCACTG[C/T]GCTATCTCTCCAGCC | 74589 |
rs226772808 | snp | C/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88549982 | GGTCCAGACAGGCAG[C/G]CATATTACCCCTTCT | 74589 |
rs226792441 | in-del | -/AGGTG | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88550488 | ACTGCATGTTATCAT[-/AGGTG]ATCTCCAAGAGCAGT | 74589 |
rs226798419 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88605264 | TGACAGTTGGTACAG[C/T]CTATGGAAGACAGTA | 74589 |
rs226832126 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88582100 | CAAAGGAAAGCCTCT[C/T]ACCTTCTGGGTCTGG | 74589 |
rs226925793 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88573794 | AAAGAGCACTGGATT[C/T]TATAGTTCTGGAGCT | 74589 |
rs226945412 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88551659 | AGCTGCCAGTGCCTG[C/T]TAAACTGTGAACTGA | 74589 |
rs226950813 | in-del | -/A | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88586198 | ACTATGAAGGTATCC[-/A]TCTGCTTTATTTACT | 74589 |
rs226963980 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609916 | AGAGCCAGGGAACAG[C/T]GCGCCTGCACTGCCG | 74589 |
rs227006920 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88602217 | TCCTGGAATAGAATG[A/G]TGACCATTATGAGAC | 74589 |
rs227014179 | snp | G/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88574925 | TGCTGTCTGTACGGG[G/T]AAATGCATATATATG | 74589 |
rs227056292 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88580054 | TCAAGGAAGAAATAA[C/T]AGGTATCCAAGATAG | 74589 |
rs227088161 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88580485 | GTAACTCTGGCTGAC[C/T]TGGAACTCACTTTGT | 74589 |
rs227167549 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88566087 | TTGACCACTGGTTTA[C/T]ATTTATAGGAGAAAT | 74589 |
rs227188327 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88550429 | CTCTTTTTCATTCTC[C/T]GTAATGTTGGCCCCA | 74589 |
rs227196910 | snp | C/G | | | downstream-variant-500B | Kbtbd12 | Mm_Celera | 6:88547459 | GCACTCTGTCCTACC[C/G]CCATGAATCCTCACT | 74589 |
rs227217462 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88604377 | ATATGTGTTCATCAC[A/T]TGGAGTGACATAAAA | 74589 |
rs227336402 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88604696 | GGTGGAGATAGGAGA[A/G]ATTCTTCAACAAATG | 74589 |
rs227362332 | in-del | -/AA | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88553904 | TGTCCTTTGTTGATT[-/AA]AAAAATCACTATTTT | 74589 |
rs227372471 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88602401 | TCCCTGAGACAAATG[A/G]ATACTGACAATAGAT | 74589 |
rs227391531 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88548312 | TAAAATGAAAATCGA[A/T]ACACCTTTAAATTAT | 74589 |
rs227391698 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88597050 | ATAGAAGAAAAGTTT[C/T]CTAACCTAAAGAAGG | 74589 |
rs227415836 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88602985 | CACAAGCAAACCCCC[A/G]TCTTTAAGGAGAATG | 74589 |
rs227425453 | in-del | -/A | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88617738 | ATGAGACCCTATCTT[-/A]ACAAAACAAAACAAA | 74589 |
rs227463408 | in-del | -/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88608050 | TGCCTCTCAAGCGTC[-/T]TTTGCATACATTTCG | 74589 |
rs227466968 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88582253 | CATTTGGAGCACATT[C/T]CCTCCTATAACGTAG | 74589 |
rs227502750 | snp | A/G | | | upstream-variant-2KB | Kbtbd12 | Mm_Celera | 6:88629242 | CATCTCAGATATTTC[A/G]TTATAGTAACTGGAA | 74589 |
rs227503329 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88574265 | CAGTTTTTCACCAGT[A/G]AGTATGATGTTAGCT | 74589 |
rs227516165 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88594472 | GTCTCTTCTATACCA[A/G]CCCAGGGCTGGCTAA | 74589 |
rs227528043 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88575529 | TATGCATGTGAATGC[A/G]GGTGCCTGTGGAAGC | 74589 |
rs227545585 | in-del | -/ATCTGTCT | | | intron-variant | Kbtbd12 | GRCm38.p3 | 6:88558968 | GTCTCTCTTGCATCC[-/ATCTGTCT]GTCTGTCTGTCTGTC | 74589 |
rs227586571 | snp | A/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88575478 | ACCTCTGAGCCATCT[A/T]AATGATGTGTCTGTG | 74589 |
rs227606212 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88611549 | ATGAATGGAGGCTAA[C/T]GGTCTCCTTCAGACT | 74589 |
rs227676564 | snp | C/T | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88609711 | TTAGAAAGTCATATC[C/T]ACCACGGGTTTCTGT | 74589 |
rs227710791 | snp | A/G | | | intron-variant | Kbtbd12 | Mm_Celera | 6:88610081 | TTATGCCCTTCCTCC[A/G]CTGACATGAATGCTC | 74589 |