SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3670396 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44130878 | ATTCTACTAAAAAAA[A/C]CTCAAAACTGACTAT | 73469 |
rs3671467 | snp | C/G | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44130999 | AGCCATCCTGACAGA[C/G]CACTGCTATTCTGAA | 73469 |
rs3671483 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Rnf38 | Mm_Celera | 4:44131011 | AGACCACTGCTATTC[C/T]GAATCTTTGGGGGTT | 73469 |
rs3671524 | snp | C/T | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44131031 | CTTTGGGGGTTTCTA[C/T]ATGCATAGGAGAAGA | 73469 |
rs3706338 | snp | C/T | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44138414 | TCTAAGTTAAGTAAT[C/T]CTCTGTGCTTCTACC | 73469 |
rs3725792 | snp | A/G | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44232801 | AAAAAGACACTGTAT[A/G]AACAGGCCTCCTTCC | 73469 |
rs6152318 | snp | G/T | 0.304688 | 0.243945 | intron-variant | Rnf38 | Mm_Celera | 4:44155525 | AACTGGTCACCAAAG[G/T]TCATAAATGACAAAA | 73469 |
rs6153428 | snp | A/G | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44155758 | TATAGTAAAGTGTTT[A/G]CCTTACAAGCTTAGG | 73469 |
rs6307101 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Rnf38 | Mm_Celera | 4:44143082 | ATGAAGCCCCAGTAA[A/G]GGCTAAGATCGTTAT | 73469 |
rs6307180 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Rnf38 | Mm_Celera | 4:44143122 | GCTACATTACTAAGT[A/C]TGATGCAAACCTTTA | 73469 |
rs6307704 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf38 | Mm_Celera | 4:44143211 | TATATATTTTAATCA[C/T]TCTAAATAAAATGTA | 73469 |
rs6308192 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Rnf38 | Mm_Celera | 4:44143276 | AATACTTATGCTGAG[A/C]TTTTTCTTATAGTAA | 73469 |
rs6308317 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Rnf38 | Mm_Celera | 4:44143357 | GTTAGCTATCCTAAG[C/T]GAGGACTGAAGAGCC | 73469 |
rs6312998 | snp | A/G | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44224609 | acagggtttctctgt[A/G]tagccctggctgtcc | 73469 |
rs6313053 | snp | C/G | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44224641 | ggaactcactctgta[C/G]accaggctggcctng | 73469 |
rs6313076 | snp | C/T | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44224655 | anaccaggctggcct[C/T]gaactcagaaatccg | 73469 |
rs6313445 | snp | C/T | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44224675 | tcagaaatccgcctg[C/T]ctctgcctcccaagt | 73469 |
rs6313472 | snp | A/G | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44224691 | ctctgcctcccaagt[A/G]ctgggattaaaggtg | 73469 |
rs6314523 | snp | G/T | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44224878 | TCAATCCTGACACAG[G/T]CACTAAGCCCAGAGT | 73469 |
rs6344903 | snp | C/T | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44138913 | AGGTCATTGTTGATA[C/T]ATCAAACTGAAAAAA | 73469 |
rs6344941 | snp | A/G | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44138936 | TGAAAAAATATATAA[A/G]TGGACCCAAGATTTC | 73469 |
rs6344978 | snp | A/G | 0.49324 | 0.0577452 | intron-variant | Rnf38 | Mm_Celera | 4:44138954 | GACCCAAGATTTCCT[A/G]TCTTTAATTATATTT | 73469 |
rs6345471 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Rnf38 | Mm_Celera | 4:44139043 | ACCCAAACTCTCAAA[A/T]TAGGAAATTAAAAGT | 73469 |
rs6345577 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Rnf38 | Mm_Celera | 4:44139102 | GAGATTTCCAGACAC[C/T]GAGCCTCCCTGAAGA | 73469 |
rs6346616 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Rnf38 | Mm_Celera | 4:44139213 | ACAGGCTGTAGTGTC[A/G]ATCAGTATGTGACTT | 73469 |
rs6363634 | snp | C/T | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44146678 | actgaccttaggtgg[C/T]catgtgtctttacct | 73469 |
rs6377242 | snp | A/G | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44146928 | ccctcttctgacctc[A/G]gcaggcactaggtat | 73469 |
rs27847714 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Rnf38 | Mm_Celera | 4:44226081 | GTATGAATGAAAAAC[C/T]GAGATAGAAAAATAA | 73469 |
rs27847715 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rnf38 | Mm_Celera | 4:44225576 | CATTCTACCCCAAAT[A/G]GCACTCCTATCCAGT | 73469 |
rs27847716 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Rnf38 | Mm_Celera | 4:44225491 | AACAGTCCTCTGCGT[G/T]CTAGCTTGCCCTAAA | 73469 |
rs27847717 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44225210 | AAGGCAACTCTGAAA[C/T]GAAACGTGTTTTACT | 73469 |
rs27847718 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44224331 | TACAGTGGTCCCGCC[G/T]CTCAGAACATCCGCA | 73469 |
rs27847719 | snp | A/C | 0.345679 | 0.230967 | upstream-variant-2KB, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44222760 | gaaagaaagaaagaT[A/C]ATTTTCACTAAAAGT | 73469 |
rs27847720 | snp | A/G | 0.46875 | 0.121031 | upstream-variant-2KB, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44221653 | GTCCTTTATCCACAC[A/G]CTAAAAAGACTCCAG | 73469 |
rs27847721 | snp | A/G | 0.152778 | 0.230321 | nc-transcript-variant, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44221239 | CCTAGATAGGCTCTC[A/G]GGTTGTTGCTGTTGT | 73469 |
rs27847722 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Rnf38 | Mm_Celera | 4:44219926 | CCATTGTCATACCCC[A/T]TCAATGAGGTGCTAT | 73469 |
rs27847723 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf38 | Mm_Celera | 4:44217824 | GAGGTTCTATAAAAA[A/G]ATTCCAGGACTTATG | 73469 |
rs27847724 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44217571 | CACACACATTCGGAA[A/G]GTCCTACAAGCACAG | 73469 |
rs27847725 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44217326 | CTGCGCACCTCTATC[C/T]TGCCACAGAAGTCAC | 73469 |
rs27847726 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44216949 | ACTGACAGGAACAGC[A/G]AGCCCTGAGAGCAGT | 73469 |
rs27847727 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44216942 | CCTGACTACTGACAG[A/G]AACAGCGAGCCCTGA | 73469 |
rs27847728 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44216746 | ATTCAGAACTCAAAA[G/T]CAGGCCATTTTTCTA | 73469 |
rs27847729 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44216583 | TCTTCTCAACTGCCC[G/T]CGTTAACCGGTCCTC | 73469 |
rs27847730 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44216523 | ATTCTGAAGCTAGAT[C/T]TGTTAAGAAACTCAA | 73469 |
rs27847731 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Rnf38 | Mm_Celera | 4:44216250 | AACACAGTTAACAGC[A/G]TCTTCACTAAGAACC | 73469 |
rs27847732 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44216173 | TAACTGCTCCCAACA[G/T]TACATGCAGTTTTAG | 73469 |
rs27847733 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Rnf38 | Mm_Celera | 4:44215750 | TGTTAACAGCAGCTT[C/T]TAGCTAAGTCTTTTT | 73469 |
rs27847734 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44215648 | TTTTTATCTCAACCG[A/C]AACTTAACAGAGTTA | 73469 |
rs27847735 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44215639 | TCACCTCTGTTTTTA[C/T]CTCAACCGCAACTTA | 73469 |
rs27847736 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44215563 | TGACTTCAGAGGTTG[C/T]TGCTGTTTGGGGTAA | 73469 |
rs27847737 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Rnf38 | Mm_Celera | 4:44215205 | CACACAGATGAGTGT[C/T]TGGAGTGTGTGTACG | 73469 |
rs27847738 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44214185 | TTTTAAATGATTTTG[C/G]TATGAGGCTGGTGAG | 73469 |
rs27847739 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Rnf38 | Mm_Celera | 4:44214057 | AAGGGAGTTTAATAG[C/T]CTTAAAATCAATTTG | 73469 |
rs27847740 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44213035 | CTCATTTTGTACTGG[A/G]AATCCATCATCTTAA | 73469 |
rs27847741 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Rnf38 | Mm_Celera | 4:44212802 | TCTCTAACTGTGAGC[C/G]GATCTCTGAGCAGTC | 73469 |
rs27847742 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44212666 | GGTAAAGCTGAGAGG[C/T]GCTGCCTAACTCAGA | 73469 |
rs27847743 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44210852 | CCAGTCTTGAGCTCC[C/T]GACTTTAGGTGTCTG | 73469 |
rs27847744 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44210840 | AGAGCGCTTAAGCCA[A/G]TCTTGAGCTCCCGAC | 73469 |
rs27847745 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44210331 | CCTGGCACACTGGCT[C/G]TGGACTGACTGAAAG | 73469 |
rs27847746 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44210310 | CATGGTGGAGTGGAC[A/G]GCTTGCCTGGCACAC | 73469 |
rs27847747 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44210244 | ACATGGACACACCAC[A/G]AAGACCAGTAAATAC | 73469 |
rs27847748 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44210104 | GAAGCAGAGGACAAG[C/G]TGTGGGTAAAGGTTT | 73469 |
rs27847749 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44209571 | CAAATAAAAAGTATT[A/T]TACGATCAGCAGCTA | 73469 |
rs27847750 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44209372 | AAACATCCCAAGAAA[G/T]TCAGGTTATCAAGTC | 73469 |
rs27847751 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf38 | Mm_Celera | 4:44209267 | AAACAGAGGAAAATA[A/G]TAAAAGGAGTCTAAA | 73469 |
rs27847752 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf38 | Mm_Celera | 4:44209218 | CTCAAAAGCCTAAAG[C/T]TATAGTTTAACTGCA | 73469 |
rs27847753 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44209062 | AATTAGCGGCAATAC[C/T]ATACTGAGAATAAAA | 73469 |
rs27847754 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf38 | Mm_Celera | 4:44209025 | CAATAAGTAAATCCA[A/G]AATGGTAAGACTTAT | 73469 |
rs27847755 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Rnf38 | Mm_Celera | 4:44208954 | TATCCTAATTAGCAT[A/G]GGAAAAAATATAAAA | 73469 |
rs27847756 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf38 | Mm_Celera | 4:44208902 | AACAAAATAGAGATG[A/G]GTATTACCTCTTACC | 73469 |
rs27847757 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44206994 | ATCCATGCAACCAAA[C/T]GCAACATTTAAGAAC | 73469 |
rs27847758 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44206753 | ATGTGGGGATCTAGA[A/G]CGCAATCTTGAGTGT | 73469 |
rs27847759 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44206733 | CTATGTAAGTGAACC[A/C]TGTCATGTGGGGATC | 73469 |
rs27847760 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44206659 | TCAGGGCTGTCTTTG[A/G]GCAGTGAAAATGTGT | 73469 |
rs27847761 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Rnf38 | Mm_Celera | 4:44206373 | AGAAGGATAGGCTAT[A/C]TATTTTGTTAATGGA | 73469 |
rs27847762 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rnf38 | Mm_Celera | 4:44206027 | ACTCTGTTCCTGACA[A/G]TGAGAAAGCCTTCAT | 73469 |
rs27847763 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44205278 | CATGAGAAAAGAATG[C/T]GTTCGATTATGTCAC | 73469 |
rs27847764 | snp | A/T | 0.487535 | 0.077957 | intron-variant | Rnf38 | Mm_Celera | 4:44205205 | AGGCCCGTCTCTGTC[A/T]GTTCTTCCAAAGGTA | 73469 |
rs27847765 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44205193 | ATTCTCTACAAAAGG[C/T]CCGTCTCTGTCAGTT | 73469 |
rs27847766 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44205107 | ATCACATCGGAACAA[C/G]GGTAAATGTGCTGAT | 73469 |
rs27847767 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44204907 | TGGGGAGAAAGGATC[A/G]AGCTGAAGGGGCTGA | 73469 |
rs27847768 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44204906 | ATGGGGAGAAAGGAT[C/T]GAGCTGAAGGGGCTG | 73469 |
rs27847769 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44204877 | ACTGATGACAGCAAA[C/G]AGCAGCTTCCGAGAT | 73469 |
rs27847770 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44204823 | CTGTTAAAGACCCAG[C/T]GAGAAGTGGCCTGGG | 73469 |
rs27847771 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44204805 | CCTGGGAAGGTAAAA[A/G]CTCTGTTAAAGACCC | 73469 |
rs27847772 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44204123 | CATGTAAAGTATGAA[C/T]TTCTTGTAAAATACA | 73469 |
rs27847773 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Rnf38 | Mm_Celera | 4:44203976 | TGGAGAATGATGTGG[C/T]GGAGAGAGATATACA | 73469 |
rs27847774 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44203460 | CCTGGCTCCCTCTGC[A/G]TTCTCAGAGCTGCAC | 73469 |
rs27847775 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44203355 | AAACTGAAAAGACAT[C/T]GGGTAAGTTCAAATG | 73469 |
rs27847776 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44203320 | AGCAGGAGCTATAGT[C/G]TCAAGTCAGAGAAAG | 73469 |
rs27847777 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Rnf38 | Mm_Celera | 4:44203262 | GAAGGGAAGAGGGCA[A/G]TAAGAAAGGAGGCTT | 73469 |
rs27847778 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44203079 | CAGGGACTGGAGAAA[C/T]GGCTCTGTACTTAAG | 73469 |
rs27847779 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44203045 | ATTGTCATCCAACAG[C/T]TACAAATATGAACAA | 73469 |
rs27847780 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44202747 | TCTCCCAATTGCAAA[A/G]ATTATAGGCACAGGT | 73469 |
rs27847781 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44201184 | TGAACAGTGTGTTCG[A/C]TTAGCAAACACTCAT | 73469 |
rs27847782 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Rnf38 | Mm_Celera | 4:44201098 | ATTAAAAGTTTTAAT[C/T]CGATACCAAATAATT | 73469 |
rs27847783 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rnf38 | Mm_Celera | 4:44201031 | GAAAAGGACTCTAAG[C/T]TAGTGACTGTGTCAC | 73469 |
rs27847784 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Rnf38 | Mm_Celera | 4:44200639 | GGGAAAATGTTTAAC[A/G]TGAGGCTGGAGAGGT | 73469 |
rs27847785 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Rnf38 | Mm_Celera | 4:44200555 | AGTATGTGGTTCAGT[A/C]CCAACAAGTACCATA | 73469 |
rs27847786 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44200521 | GCTAAAGTATGGATT[A/G]GTGGTAGAGTTACTA | 73469 |
rs27847787 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44200503 | AAGGGAACATACTGA[G/T]AAGCTAAAGTATGGA | 73469 |
rs27847788 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Rnf38 | Mm_Celera | 4:44200168 | ATGCTGCCACCAGGT[A/G]GCAAGAGCATGTTAT | 73469 |
rs27847789 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44199900 | CATGTACTTACATGC[C/T]ATCATACACTGTCCT | 73469 |
rs27847790 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44199881 | TTACACTATCCAGCC[C/T]GCTCATGTACTTACA | 73469 |
rs27847791 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44199804 | CTGACTTAAAAAGCC[G/T]GGTCTGTTTTCTTCC | 73469 |
rs27847792 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44199655 | GCTGCTGCAACTACA[A/C]ATGGCTTAAAACTTT | 73469 |
rs27847793 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44199460 | TGAATGAGTACTTTA[C/T]GTTACTAAAAATTTT | 73469 |
rs27847794 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44199395 | TCTGGTCAGGCACAC[C/T]AGCAAACACTCAACA | 73469 |
rs27847795 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Rnf38 | Mm_Celera | 4:44199334 | AGCCCATTAGCATAC[A/C]CTGGGCTACATCCTA | 73469 |
rs27847796 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44199298 | TTAAGCATTTGTTTA[C/G]AGAGATGTGATTTAT | 73469 |
rs27847797 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44199271 | GCTGCTTCCAGCTCT[G/T]GAAAATTATTTTTAA | 73469 |
rs27847798 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44198676 | ACAAATTAGGAATGC[A/C]TTATCAAGCAAGGAT | 73469 |
rs27847799 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Rnf38 | Mm_Celera | 4:44198642 | TTAATAAGCAAACTT[A/G]TCCCAAGCAGAAACT | 73469 |
rs27847800 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Rnf38 | Mm_Celera | 4:44198555 | AAAACCTCAATAACT[G/T]GATTAATTCTATAGA | 73469 |
rs27847801 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Rnf38 | Mm_Celera | 4:44198304 | AACTCTTTTTGCGGG[C/T]TTGTTGGTTTGTTTG | 73469 |
rs27847802 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44198272 | CCAAATAAAAAACAA[C/G]CCCAAACCTATTGGT | 73469 |
rs27847803 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44195130 | AAGACAAGGTGTCAG[A/T]GGGACTCTAGGACAC | 73469 |
rs27847804 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44195013 | CAGAAGCAAAGAAAA[A/G]GGAGGAAAAGACATA | 73469 |
rs27847805 | snp | A/C/G/T | 0.391111 | 0.206368 | intron-variant | Rnf38 | GRCm38.p3 | 4:44194689 | AGATTTCCTAGGCTA[A/C/G/T]GGTGGGAATATAGCT | 73469 |
rs27847806 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Rnf38 | Mm_Celera | 4:44193713 | TAGATGTTTAACCAC[C/T]AACTTTAAATACCAT | 73469 |
rs27847807 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Rnf38 | GRCm38.p3 | 4:44193297 | CCTAGTACTAGAAAC[A/G/T]TGGCCAAAGGCTCAG | 73469 |
rs27847808 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Rnf38 | Mm_Celera | 4:44193262 | CACCAGATACTTCCT[C/T]ACTCATACAACTACA | 73469 |
rs27847809 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44193130 | AAATCGGCTGATACA[C/T]AAGATGTCAATCACT | 73469 |
rs27847810 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44193069 | CCTCGAAGATATCTA[C/T]TGTGACCTCAACTCT | 73469 |
rs27847811 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44193000 | GGGAAGGGAAAAGCA[A/T]GCCCTTCTCTGTGAT | 73469 |
rs27847812 | snp | C/G/T | 0.244898 | 0.249948 | intron-variant | Rnf38 | GRCm38.p3 | 4:44192953 | GCGGATACTCGCCTA[C/G/T]GTGCCCAGGGACCTG | 73469 |
rs27847813 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44192928 | AAAGGCAGGCACAGC[A/G]CTATGACGGGCGGAT | 73469 |
rs27847814 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44192493 | GCCCTCCACACCCAT[A/G]CCATGGCACAACCAC | 73469 |
rs27847815 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44192431 | GTAACACAACGGAAA[A/G]ATGCTGCCTCAAACA | 73469 |
rs27847816 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44192360 | TAAGGGCACATCTGA[C/T]GACGGGAACTGACCT | 73469 |
rs27847817 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44192354 | AGCACTTAAGGGCAC[A/G]TCTGATGACGGGAAC | 73469 |
rs27847818 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44192335 | AGATCTCTCGGTGGG[C/T]AAAAGCACTTAAGGG | 73469 |
rs27847819 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf38 | Mm_Celera | 4:44192245 | AAGATAATGGGACAG[C/T]GACATGTCTTTGTAT | 73469 |
rs27847820 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44191805 | CCTTTCTCTACATCT[C/T]CCAAAACTGTCATAG | 73469 |
rs27847821 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44191792 | ACAGTGCCAACTTCC[C/T]TTCTCTACATCTTCC | 73469 |
rs27847822 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44191373 | TAAGATTAAGCAAAT[G/T]AAAAAGCTAGTAACA | 73469 |
rs27847823 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44191295 | AAATCCCATGCCTCT[C/T]TCACTGGAAAACTAG | 73469 |
rs27847824 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | GRCm38.p3 | 4:44190740 | ACAATTATCGAAGGA[A/G]CAAATATACAAACTC | 73469 |
rs27847825 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44189792 | CAAATCTGAACAAAA[A/G]CCTTACTTATACGTG | 73469 |
rs27847826 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44189375 | GCCTATCTCAAGGTG[A/G]AAGGCAAGGACTGAA | 73469 |
rs27847827 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44188839 | GAGGGTAAGACAGGA[A/G]TATTGAAAGTTAAAG | 73469 |
rs27847828 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44188706 | GTGTATTGACTGTGG[A/T]TGGGTCCATAATGCA | 73469 |
rs27847829 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44188009 | TAACTTTTCAGACAC[A/G]CAAGAGCTTCCTAAT | 73469 |
rs27847830 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44187331 | CCCTGTACTGTGCAT[A/C]TCAACATTATACCCT | 73469 |
rs27847831 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44187199 | GAGGAAGGACAGAGA[C/T]ACAAACGGGGGATTG | 73469 |
rs27847832 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44187127 | AACTGCTTTGCTGCT[A/G]AGAGAGCACATGTTC | 73469 |
rs27847833 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf38 | Mm_Celera | 4:44186536 | GATAGGTTACATTCT[C/T]AATAACCAAGGTTTA | 73469 |
rs27847834 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44186478 | TGAAACAACTTGGGC[C/T]CAAAGTAACACACAC | 73469 |
rs27847835 | snp | C/G | 0.33241 | 0.236027 | intron-variant | Rnf38 | Mm_Celera | 4:44185736 | ACTCTGGAAGGCTAT[C/G]AACAGAGCTGACAAA | 73469 |
rs27847836 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Rnf38 | Mm_Celera | 4:44185461 | AGACAGAATCTCATC[C/T]CCAGACTGTACGGCC | 73469 |
rs27847837 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Rnf38 | Mm_Celera | 4:44184948 | AGATGCCCTTTGGTA[C/T]GTTGACAAAACATAA | 73469 |
rs27847838 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44184828 | ACTACTTGCTGGCTC[A/G]AATCAACAGAATAAG | 73469 |
rs27847839 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44184788 | ATATTCTCTAAATGA[C/T]TCACCACATAGCTAC | 73469 |
rs27847840 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Rnf38 | Mm_Celera | 4:44184165 | GTTGGAAAGCCCCAA[C/T]TCCACATACACTTCC | 73469 |
rs27847841 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44182602 | CCTGTTTTCTAGTGT[A/G]TTAGACAAGTAACAG | 73469 |
rs27847842 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Rnf38 | Mm_Celera | 4:44182330 | GGACACAAGCCCTTG[A/G]CTCTCAGAAGAGACA | 73469 |
rs27847843 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44182259 | CTTTAAGGCAGTTCT[A/G]TGTTGGTGCCTCATG | 73469 |
rs27847844 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44182246 | GGGTAAGCTGAATCT[A/T]TAAGGCAGTTCTATG | 73469 |
rs27847845 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Rnf38 | Mm_Celera | 4:44182108 | AGGAGTCTGTGAGTG[A/G]CTCAAACTGGGACTC | 73469 |
rs27847846 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44182067 | TGTCTGTGTGAGTAT[A/C]CCTTCATTCTTTGGT | 73469 |
rs27847847 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Rnf38 | Mm_Celera | 4:44181884 | TGTGTAATCAGCTGC[A/G]GCTTCTTCCTCCTAG | 73469 |
rs27847848 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Rnf38 | Mm_Celera | 4:44181746 | GCGTGCCTGGCATGG[C/T]CACAGCCACATCAAG | 73469 |
rs27847849 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44181553 | TTTTCTCACTATCAA[C/T]CTATGAGTACCTTAA | 73469 |
rs27847850 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Rnf38 | Mm_Celera | 4:44181245 | GGGATCCATCTTACT[C/T]TTAACTGCTATTTTT | 73469 |
rs27847851 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44181005 | AGCTTCCCAAGGGCC[A/G]GGCTCTGAGGTACTC | 73469 |
rs27847852 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44180909 | TGTGCTCACGCCCAC[A/G]TTACACCCTCTTTGC | 73469 |
rs27847853 | snp | A/C | 0.465374 | 0.126941 | intron-variant | Rnf38 | Mm_Celera | 4:44180760 | TTCTACTAAAAGTGT[A/C]GCCTCTATTTGGGTA | 73469 |
rs27847854 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Rnf38 | Mm_Celera | 4:44180646 | CATTAACACAAAGCA[C/T]GTACCATAATAGCAA | 73469 |
rs27847855 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44180570 | ATGGCCAGCTCGAAG[G/T]CAGAGACAAAATTAG | 73469 |
rs27847856 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44180289 | TACTCCAAGCCTGGC[C/T]ACTGGATTCTCTCAT | 73469 |
rs27847857 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44179803 | CGGTACTTCACCTCA[A/G]CTCTCTCTGTCTCCC | 73469 |
rs27847858 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44179629 | AGTACACTTTTTCCC[C/T]GGGCTTTTATCATTT | 73469 |
rs27847859 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44179498 | CTGTTTAGCCATTGT[A/G]GCAACATTGTAAGGA | 73469 |
rs27847860 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44179287 | TTAGCAGAGAGGCAC[A/G]CTGTGATCACATGAC | 73469 |
rs27847861 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44178886 | CATGGAAAAATGATA[A/G]GTGTAATTCAAAACA | 73469 |
rs27847862 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44178873 | ATGTACACACACACA[C/T]GGAAAAATGATAAGT | 73469 |
rs27847863 | snp | A/G | 0.18 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44178597 | CCTAACTAAGACCCT[A/G]AGTTTGTTTGTTTGT | 73469 |
rs27847864 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44176808 | ATAATAAATATGTCA[C/T]GTAACAAACAATAGT | 73469 |
rs27847865 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44176075 | GCCTAAGCAGAATTA[A/T]AATTACCACAAATCA | 73469 |
rs27847866 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44175930 | CCTGCCACTGATACA[G/T]TTTTATAATGCAGCC | 73469 |
rs27847867 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf38 | Mm_Celera | 4:44175926 | AGCTCCTGCCACTGA[C/T]ACAGTTTTATAATGC | 73469 |
rs27847868 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44175922 | CAGTAGCTCCTGCCA[C/T]TGATACAGTTTTATA | 73469 |
rs27847869 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Rnf38 | Mm_Celera | 4:44175884 | GTATCACACACAGGA[A/C]ATGTAACCTGCTCAG | 73469 |
rs27847870 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44175849 | TGTGTCAGCATCATC[A/G]CAACACTGCAGGGGG | 73469 |
rs27847871 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44175736 | GATACAAGGCATAGG[A/G]CATGTTCTTGGTGGA | 73469 |
rs27847872 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44175709 | CGGGGATGAGGTCCT[A/G]GAAGGGTTTTAGATA | 73469 |
rs27847873 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44175689 | CAGGGGTAATCACCG[A/G]AACACGGGGATGAGG | 73469 |
rs27847874 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44175530 | AGCCAGAAGCAGCAA[A/G]ACATTAAGGAAAAAT | 73469 |
rs27847875 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44175461 | GACCTGCTGGAAAGA[C/T]AATCCTCAGGGCAGA | 73469 |
rs27847876 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44164140 | ACAGTCTTCTGTGCC[A/G]GCTTTTTTGTCTGTT | 73469 |
rs27847877 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44163881 | AACTCACCCGGTGTA[C/G]CTGGAAAGTAAGACT | 73469 |
rs27847878 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44163452 | GTTTAATTGAACTGA[C/T]TAAAAAGGCATGCAC | 73469 |
rs27847879 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Rnf38 | Mm_Celera | 4:44162665 | GGGACTCAAACTTTC[C/T]TTACGGAAGCATAAA | 73469 |
rs27847880 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf38 | Mm_Celera | 4:44162323 | AATGATTTTAAAAGA[A/G]AACAACCAAGGAAAG | 73469 |
rs27847881 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44162293 | GGCCAGAGCAGTTAC[C/T]ATAATCTGTCAACCA | 73469 |
rs27847882 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44161268 | AAAGAGATAAGACGT[A/C]TATTTGCCATTCTTG | 73469 |
rs27847883 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44161059 | ACAGTATGATATTCA[C/T]GCACTATAAAGCAGG | 73469 |
rs27847884 | snp | C/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44161018 | TAAGCGTGAAAAGGG[C/G]AGGACAGAATGGATG | 73469 |
rs27847885 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44160499 | TAGTACTGCCATGCT[A/T]TGATCATCTCTGACC | 73469 |
rs27847886 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44160415 | AAAAAAGAAAACACA[A/G]CTCTCAGAATGGCAG | 73469 |
rs27847887 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44159990 | TTTTACAGTTTTTTC[C/T]CTCAGTCTTAGATCT | 73469 |
rs27847888 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44159886 | TGTGACAGTGAAATT[C/T]TCCTTGGGGACTCCA | 73469 |
rs27847889 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44159794 | GTAACGTAAAAATCT[A/G]GACTGTAGTTTAAAT | 73469 |
rs27847890 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44159679 | AAAGCAAATGAAAAT[C/T]CTCAAACAGTAACAA | 73469 |
rs27847891 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf38 | Mm_Celera | 4:44159482 | CAGCTGAAAGACTGT[A/G]TGTACTTCATGTACA | 73469 |
rs27847892 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Rnf38 | Mm_Celera | 4:44159379 | GAGTGATGAATGTTT[A/G]CCTACACTGTATTTT | 73469 |
rs27847893 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44159208 | AAATACAGGCTGCAC[A/G]AACGGTCTCTAGCAA | 73469 |
rs27847894 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44159164 | GTTCTGTCAGCAGAC[A/G]GGGCAGGGCAAGAGG | 73469 |
rs27847895 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44159138 | GGAGAGCTGAGGTTT[C/T]GAGTGTGATAGTTCT | 73469 |
rs27847896 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44159103 | GCTGGCCATACTGAC[A/T]TGGAGAACAAGCCTA | 73469 |
rs27847897 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44158547 | ATGTTCTGGGCACTA[A/C]GCAAGCAGTGATGGC | 73469 |
rs27847898 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44158141 | AAATCAGATGAGGCC[C/T]TTGCTCTACAAATAA | 73469 |
rs27847899 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Rnf38 | Mm_Celera | 4:44157990 | ACAAACAAACAACAA[C/T]CCAGTAGTCAATGTG | 73469 |
rs27847900 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44157209 | GAATATGGAGAACAC[A/G]GAAAATGAGAAGTAT | 73469 |
rs27847901 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44157026 | ACTAACATGGGCAAA[A/G]ATCTCAATTCAACTG | 73469 |
rs27847902 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44156958 | AGGGATTAGAGTATA[C/T]GATATGACTAGTTAG | 73469 |
rs27847903 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rnf38 | Mm_Celera | 4:44156844 | GAGAAAACTCTCTGG[C/T]TCTCCCCTAAAGAAT | 73469 |
rs27847904 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rnf38 | Mm_Celera | 4:44156518 | CTTCTCGTGTAGTAA[C/T]AAGGTTTTATTTTTA | 73469 |
rs27847905 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44156450 | AAAGTAAAAGGTATC[G/T]ATGGAAAGCCAGTCA | 73469 |
rs27847906 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44155886 | CTGCCTTGTCTCCAC[A/G]CTAGTGAAAACTATC | 73469 |
rs27847907 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44154984 | TAGAAACCACTGAAC[G/T]TTTTGAGGACTACAT | 73469 |
rs27847908 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44154902 | CTGGGAATCAAGGGT[A/G]GAAAGGAGGCAGGAA | 73469 |
rs27847909 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44154859 | TAAAACCTACAGCTA[C/T]TACCTCTACTATCCA | 73469 |
rs27847910 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44154744 | TGGGCCTGTCTTTTC[A/G]AAAAAATTTGTTTTG | 73469 |
rs27847911 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44154718 | ACTCAGAAAACGACT[A/G]AATTATTAGATGGGC | 73469 |
rs27847912 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44154701 | GGTGCTACTAGAACC[A/G]AACTCAGAAAACGAC | 73469 |
rs27847913 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Rnf38 | Mm_Celera | 4:44154647 | CCCACCTACCTAATA[C/T]GAATTGCTACTTCTG | 73469 |
rs27847914 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44154357 | CCAGCACACATGCAC[A/G]CATGCACACGTATGT | 73469 |
rs27847915 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44153817 | TTAAGAAGACAAGCA[A/C]AGAAAACAACTGATT | 73469 |
rs27847916 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44152779 | TGTTTGGAAAAACCA[A/C]ATTAGATGACAACAT | 73469 |
rs27847917 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Rnf38 | Mm_Celera | 4:44151265 | AGGTACCTCAACTCA[C/T]ACTGATTTTCTTGAA | 73469 |
rs27847918 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44150074 | ATGACTATTAACCAA[A/T]AGCAGGTGAATAAAT | 73469 |
rs27847919 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44149799 | TTGACCACTTGTATG[A/G]AATCATGGGTAGATA | 73469 |
rs27847920 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf38 | Mm_Celera | 4:44148914 | GAGAACTCAAGCAAG[C/T]TACATTTCAGGAATT | 73469 |
rs27847921 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44148811 | CTAACTCGTTTCATG[G/T]TCCTTTATTTTCTCT | 73469 |
rs27847922 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf38 | Mm_Celera | 4:44148787 | TTTGAAGTACTCTTC[A/G]AAATAACACTAACTC | 73469 |
rs27847923 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Rnf38 | Mm_Celera | 4:44148671 | TTACTTAAGAACTGT[A/C]AGGTTTTACAAAACT | 73469 |
rs27847924 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44148524 | TACAAAAACAACTAG[C/T]AACAGCTTGCTTTCA | 73469 |
rs27847925 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rnf38 | Mm_Celera | 4:44148354 | CACACATTAAAAAGG[A/G]AAAAAATCATGAGAG | 73469 |
rs27847926 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44147742 | GTGGTTAGATGTTTG[G/T]CTTAAGTACAAAAAC | 73469 |
rs27847927 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44147700 | TCCTAAAAATTGAAA[A/G]TAAAACTGGAAATGT | 73469 |
rs27847928 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44147596 | TCTTCCAAATTCAAC[C/T]ATCGCCATATATCAA | 73469 |
rs27847929 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44147485 | TTTGCTTACTTTTTA[C/T]GTGCTCTTATTTAAG | 73469 |
rs27847930 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44147318 | ATGGAGCCAGAGTTC[A/C]AACTCATTCACATGG | 73469 |
rs27847931 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44146178 | TCTCCTCAAAGATCC[A/G]TGTTACTAACATGCT | 73469 |
rs27847932 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44146177 | CTCTCCTCAAAGATC[C/T]GTGTTACTAACATGC | 73469 |
rs27847933 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44145092 | AAAACTTAGTGCTAT[A/G]TTAACTCTTTCAGCC | 73469 |
rs27847934 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44144564 | CTTTCTCTAGTAGTG[C/T]CAATAGAAAGGTTTT | 73469 |
rs27847935 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44144399 | TTCACACTCACATTG[C/T]ACTTTCGCCATATTT | 73469 |
rs27847936 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44144365 | TATCAAACAAATTTA[C/T]TGATTCCCTTATTTG | 73469 |
rs27847937 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Rnf38 | Mm_Celera | 4:44143574 | CCCATGGGGTGCCAC[C/T]GTAGTTACCGTGTAG | 73469 |
rs27847938 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44142854 | ACTTAAGATTTTTTC[C/T]AAGTGCTTTCCCCTT | 73469 |
rs27847939 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44142001 | TAGAAAAAACCCTAG[A/T]ACCAATTAGAGAAGA | 73469 |
rs27847940 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Rnf38 | Mm_Celera | 4:44141745 | ATTAAGGACAGACAA[G/T]TAAAAGGTTTCCAAC | 73469 |
rs27847941 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44141326 | ACTTCGTAGCATGCA[C/G]TGTGTTAATAAATAA | 73469 |
rs27847942 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Rnf38 | Mm_Celera | 4:44141252 | aaaactagccaatac[A/G]ACACACAAGGAGAAT | 73469 |
rs27847943 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44139159 | AGAAGTAGAACCAGG[A/G]GGCACAGTACAGTAC | 73469 |
rs27847944 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44139135 | TAACATATAGTATGT[G/T]TGTAAGTCAGAAGTA | 73469 |
rs27847945 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44138608 | ATTTCCAGAATTATA[C/T]TGAAAACTCAAAATA | 73469 |
rs27847946 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44137706 | TTCTATGTTTAAAAT[C/T]AGTGTCAAATAATAT | 73469 |
rs27847947 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44137488 | ACACATAGTAAGTCA[C/T]AGGCCACAGCGAGGG | 73469 |
rs27847948 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44137449 | CTCAAGTCCAACTTA[A/C]CATCAAGCAAAAGCA | 73469 |
rs27847949 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44137426 | ATCTTCTTCCTTAAT[C/G]ACTGGCTCTCAAGTC | 73469 |
rs27847950 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44136825 | CTACCATGTTTAACC[A/G]ATGATGTTCATTACA | 73469 |
rs27847951 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44136749 | AGAAGAATCCACTCC[C/T]ACAGACACAAGGGGA | 73469 |
rs27847952 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44136440 | GAAAAATAACCTGTA[G/T]TTTAAAGATGACATT | 73469 |
rs27847953 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Rnf38 | Mm_Celera | 4:44136391 | GAGAGAACGGTGTGC[A/G]GTAAGGGAAAAGAGG | 73469 |
rs27847954 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Rnf38 | Mm_Celera | 4:44134917 | AACTTCTCCGTCTTC[C/T]ACATCTAATTCAAAG | 73469 |
rs27847955 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44134828 | CCTCATAAATATTTA[C/T]GTGAAAGTACAGGAC | 73469 |
rs27847956 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44134592 | CACTTTCCTCTCTCA[A/G]CCATATGCAAAAATC | 73469 |
rs27847957 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44134434 | AATCTCCATTTTCTC[C/T]CATTTTTAAGACAAG | 73469 |
rs27847958 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44134341 | TTAGGCTGCCTTTTT[A/T]AATAAAGATTAAGTA | 73469 |
rs27847959 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44134248 | TTGATGTATCTTATT[A/G]TGTTTATCGATTTTA | 73469 |
rs27847960 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rnf38 | Mm_Celera | 4:44134162 | TGGGTAACTTATCTA[C/T]ACCAAATTGTAAAAA | 73469 |
rs27847961 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Rnf38 | Mm_Celera | 4:44133788 | GAGACAGATTTTCAT[A/C]TTTACCTTTTCTATT | 73469 |
rs27847962 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44133622 | CTAAAGGTAGAAGTG[C/T]CACAGAAACATACTT | 73469 |
rs27847963 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44133290 | TATCAGTCACTTGCT[A/G]TTGTAACATTGGGAA | 73469 |
rs27847964 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44132748 | AGTATGAGGAGCACT[A/G]TGTTACAGGGTTCCA | 73469 |
rs27847965 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44132733 | TACCACAAACACATA[A/G]GTATGAGGAGCACTA | 73469 |
rs27847966 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf38 | Mm_Celera | 4:44132553 | GTTGTATAAATGTAA[A/G]GACCAGAGTTCACAT | 73469 |
rs27847967 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44132253 | ATTACCCTTACAAGT[A/C]CTGGAATAAGGTTGA | 73469 |
rs27862968 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44132206 | AATTAACATCCCAGT[C/T]GGTCTGAAAACTAGA | 73469 |
rs27862969 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Rnf38 | Mm_Celera | 4:44131792 | CTTTCTGAAGGTTCT[C/T]TGATTTACTGACGAC | 73469 |
rs27862970 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44131744 | TCACTTTAAAAAAAT[G/T]ACCACTTTCCTAAAC | 73469 |
rs27862971 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf38 | Mm_Celera | 4:44131697 | TTGTTATGACTATTA[C/T]GTTTGCAAGGCTATT | 73469 |
rs27862972 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf38 | Mm_Celera | 4:44131443 | GCTTCCAGTTCATCT[C/G]CTGTACCCTCAGCCT | 73469 |
rs27862973 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44131232 | GTGTGAAACTGCCAC[C/T]CTGTTGATGGCAACA | 73469 |
rs27862974 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Rnf38 | Mm_Celera | 4:44130588 | AGCATGAGCTCCTCC[A/G]TGCTTCAGAATGACT | 73469 |
rs27862975 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Rnf38 | Mm_Celera | 4:44130546 | TTTGTAAAACAGCTG[C/T]GGTAGGTAGCGCCCT | 73469 |
rs27862976 | snp | A/G/T | 0.244898 | 0.249948 | intron-variant | Rnf38 | GRCm38.p3 | 4:44130510 | TTTCCTGTCTCATTC[A/G/T]CTACACTGTGGCCAG | 73469 |
rs27862977 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Rnf38 | Mm_Celera | 4:44130344 | AAGGCATCACTTACT[A/C]TCTTAGCTGCTACGG | 73469 |
rs27862978 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf38 | Mm_Celera | 4:44129725 | GCCCAGTTCTCCTGT[C/T]CCTCCCAGATGGTCT | 73469 |
rs27862979 | snp | A/T | 0.18 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44129691 | ACGCTCACTGAAGCC[A/T]TGTCTCATGCAGTGA | 73469 |
rs27862980 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44128847 | AGTGACCCACTCAGG[A/G]TCACCAAGGAAGAGA | 73469 |
rs27862981 | snp | C/T | 0.475309 | 0.108333 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44128819 | GGAGTGAGAATCTGA[C/T]ACTTTTTCCTTAAGT | 73469 |
rs27862982 | snp | G/T | 0.244898 | 0.249948 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44128372 | AGAGCAGCTCAGGAC[G/T]GGAGTGTGTCAACTC | 73469 |
rs27862983 | snp | A/C | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44128267 | ACATCAAAGCAAACC[A/C]GGCCTGAGAAATGAG | 73469 |
rs27862984 | snp | A/C | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44127964 | CTGCACACGTGCTGA[A/C]AACTCACAGAGGCTG | 73469 |
rs27862985 | snp | C/T | 0.33241 | 0.236027 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44127297 | AGGCTACTTTCCAGT[C/T]GTGAGCACAGTGTGC | 73469 |
rs27862986 | snp | A/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44127153 | TTCCCAGGAGACAGC[A/T]GTCATCTGCACAGCA | 73469 |
rs27862987 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44127097 | AGCCTAAGCCCTCCA[C/T]GAGCAGGTCTGCACA | 73469 |
rs27862988 | snp | C/G | 0.32 | 0.24 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44127045 | TACAAAGATGCTCAC[C/G]GAGGCCATGGAGACC | 73469 |
rs27862989 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44126981 | TCTGTCGCCTGGTGC[A/G]CCTCCCCACGTGATG | 73469 |
rs27862990 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44126972 | ACCACATCCTCTGTC[A/G]CCTGGTGCGCCTCCC | 73469 |
rs27862991 | snp | G/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44126947 | GCCAATCAGTCCTAG[G/T]AGGAAGGCCACCACA | 73469 |
rs27862992 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44126929 | CTGGGTTAGGACGGC[A/G]ACGCCAATCAGTCCT | 73469 |
rs27862993 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44126926 | CAGCTGGGTTAGGAC[A/G]GCGACGCCAATCAGT | 73469 |
rs27862994 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44126746 | AGTTGTTTTGTGGAA[A/G]TTGGAGTTTTTAAAA | 73469 |
rs27862995 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44126725 | TCTTGATACTTGGAG[A/G]CCTTGAGTTGTTTTG | 73469 |
rs27862996 | snp | C/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44126547 | ATGCACGGTGGGACA[C/G]ACTAAGGAAGGCCTG | 73469 |
rs27862997 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Rnf38 | Mm_Celera | 4:44126203 | CACGCCTTACATGAA[A/G]CACGACTTAGGTTTG | 73469 |
rs27862998 | snp | G/T | 0.124444 | 0.216185 | downstream-variant-500B | Rnf38 | Mm_Celera | 4:44125914 | TACTTCCTTTTCCGG[G/T]TACCTGGGATGTTTC | 73469 |
rs27862999 | snp | A/T | 0.124444 | 0.216185 | downstream-variant-500B | Rnf38 | Mm_Celera | 4:44125777 | TTTGCTCAAGTTACC[A/T]GGTCAGCATATTGCT | 73469 |
rs31746895 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44213314 | AGTATACCAACACTG[C/T]CCACCCTTTTAGGGG | 73469 |
rs31757220 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44224721 | GTGTGCCACCACTGC[C/T]GGGCTCTTTTCCTTT | 73469 |
rs31761367 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44223530 | TTTTTGTTTTTTTTT[C/T]CTACTGTTACAAATT | 73469 |
rs31774484 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44163290 | CAGTCTCTACTTCTG[C/T]TCCTGGCCTAACTTC | 73469 |
rs31799385 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44151842 | CTGCTCAGACACTGG[C/T]TGATCAGCTTTTATT | 73469 |
rs31847293 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44203860 | AGAGAGAGAGAGAGA[C/G]AGACAGACAGACAGA | 73469 |
rs31890239 | snp | C/T | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44196721 | AGTAGTGGCTGACTT[C/T]AATATCCAACTAATC | 73469 |
rs31910434 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44156835 | AAATGAGTAGAGAAA[A/G]CTCTCTGGTTCTCCC | 73469 |
rs31919275 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44202327 | AGATAGATAGACAGA[C/T]AGACAGACAGACAAT | 73469 |
rs31943868 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44135247 | GATGATGAGAGAACC[C/T]AACTCTCACAAGTTG | 73469 |
rs31949246 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44158677 | AAAGATTTTTTTTTT[A/T]AAAAAACAGAGTATT | 73469 |
rs31990176 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44151760 | GCCTCAGATGTGTCT[A/C]CCCAACCTTCCTTGA | 73469 |
rs32004932 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44221749 | ATCCCCTTGTTGCCC[A/G]AGCTACCCTCAACTC | 73469 |
rs32022531 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44208560 | CCTGGAACTCAGAAC[C/T]GCCTGCTTTGCACTA | 73469 |
rs32086460 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44181437 | TAACTAGCCCTCTCC[C/T]GCCTACTTGTAGGCT | 73469 |
rs32101642 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44134467 | CTTACTATGTAGTTC[A/G]AACTTACTTTAAATG | 73469 |
rs32109031 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44219920 | GCTAGCCCATTGTCA[G/T]ACCCCTTCAATGAGG | 73469 |
rs32139660 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44203618 | AGCTATCAGGCTTAG[A/G]GACAAAACAATTACC | 73469 |
rs32155425 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44203381 | AAATGTGGTAATGGG[A/G]GGGCAGGTGTGGCTC | 73469 |
rs32161141 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44165887 | CAAGCAGAAAATTTG[A/T]AAACAGCACCAGAGA | 73469 |
rs32180759 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44162458 | GTCTTACTATATATA[A/T]AACTTAGGCTGGCCT | 73469 |
rs32231137 | snp | C/G | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44203836 | ACACACACACACACA[C/G]AGAGAGAGAGAGAGA | 73469 |
rs32244984 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44200063 | AACCAAAAAAAAAAA[A/G]AAAAAAAAATCTGTA | 73469 |
rs32282547 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44151057 | ACAAATTCTATTAGA[C/T]AAGGGCCCCGTCCTT | 73469 |
rs32321422 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44184641 | CCACCTTTTCTTTTA[A/T]CTAGTTCTTATTGTA | 73469 |
rs32371441 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44219051 | CCAGCCTGGTCTACA[A/G]AGTGAGTTCCAGGAC | 73469 |
rs32371464 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Rnf38 | Mm_Celera | 4:44169932 | GAACTAACATTTTTA[A/G]AGCTGCATATCCAGC | 73469 |
rs32385124 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44207791 | GCCACATGGTTGCTG[A/G]GAACTGAACCCATGT | 73469 |
rs32415033 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44131278 | AAAAAAACCCAAAAA[A/C]CCAAAAAACCCAAAA | 73469 |
rs32424487 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44218973 | GCATGAATAGTAGTG[A/G]TGGCACACGCCTTTA | 73469 |
rs32536038 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Rnf38 | Mm_Celera | 4:44168493 | GCCCGGCGGCAGCTC[C/T]CGCTCCCGCCAGCAA | 73469 |
rs32546865 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44210490 | AGCACCAAAAACCAA[C/T]GTGGTGTAAGACATG | 73469 |
rs32563174 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44184374 | ACTCACTTTATAGGC[C/T]AGGCTGGCCTCAAAC | 73469 |
rs32616000 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44171107 | TCTTTATATTCAGCT[A/G]AAAATAACAAAACTA | 73469 |
rs32628658 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44182497 | CACACACATAGATAC[A/C]GACACACACACACAT | 73469 |
rs32665214 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Rnf38 | Mm_Celera | 4:44168956 | GAAAGAGGACGAATA[C/G]GAGCTTTAGGTCCGC | 73469 |
rs32672972 | snp | A/C | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44194315 | AACCCTGTCTCAAAA[A/C]AAAACAAAACAAAAC | 73469 |
rs32674008 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44159662 | AAAAAAAAAAAAAAA[A/G]AAAAGCAAATGAAAA | 73469 |
rs32679137 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44184540 | AAACTTGCTATGTCA[A/G]TCAGGCTGGCCTGGA | 73469 |
rs32697642 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44208721 | CTCTCTCTTCTACAA[A/G]GCATACATATTTAAT | 73469 |
rs32700055 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44149599 | AAAAAAACTGGGGGT[G/T]GGGGGAAGAGGTGTG | 73469 |
rs32736916 | snp | G/T | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44196621 | CACAGCGGACATCAC[G/T]ACTCTAGCATGTGTG | 73469 |
rs32739202 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44208653 | AGTTCTGTTTCCAGC[A/G]CCCACATCAGGCAGC | 73469 |
rs32781203 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44195240 | TGTAGCCCTTGCTAT[C/T]CTGGAATTCCATTTA | 73469 |
rs32784859 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Rnf38 | Mm_Celera | 4:44168478 | CGCAGGGAGTGCCTA[A/G]CCCGGCGGCAGCTCC | 73469 |
rs32788499 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44133405 | TCTGTAATGAGATCC[G/T]GTGACCTCTTCTGGC | 73469 |
rs32806654 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44186254 | CAAAACAAAAACCAC[A/G]CACAAGCAAAAACAA | 73469 |
rs32836318 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44218978 | AATAGTAGTGGTGGC[A/G]CACGCCTTTAATCCC | 73469 |
rs32852415 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44221732 | TTGTTTTGAGCAGCG[A/G]AATCCCCTTGTTGCC | 73469 |
rs32858599 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44204649 | GAGCCTGTCTCAAAA[A/C]TGTACATCAGTGGTA | 73469 |
rs32862528 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44133849 | TGTGTGCACCTGAAT[A/G]CACACATGTGGCACC | 73469 |
rs32867958 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44196104 | CACAGAATATACTTA[C/T]AGCAATCTTTTTGAC | 73469 |
rs32893805 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Rnf38 | Mm_Celera | 4:44168651 | TTGTCCAACCCTCAG[A/G]ACGACGGTGACAGAT | 73469 |
rs32922792 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44138095 | TCTGCCTCAATGCTA[A/G]AATAAAATACAACTT | 73469 |
rs32928014 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44231520 | AAACGCTCACACATG[C/T]AAAATAAACCTATTA | 73469 |
rs32928016 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44181438 | AACTAGCCCTCTCCT[A/G]CCTACTTGTAGGCTG | 73469 |
rs32930786 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44219690 | TAAGGGCCAAGAATC[C/T]CTGGGGGCTGGCGAG | 73469 |
rs32988910 | snp | C/T | 0.5 | 0 | intron-variant | Rnf38 | Mm_Celera | 4:44196633 | CACGACTCTAGCATG[C/T]GTGCCAGCACAGGTG | 73469 |
rs32998778 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44202323 | AGATAGATAGATAGA[C/T]AGACAGACAGACAGA | 73469 |
rs33003541 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf38 | Mm_Celera | 4:44172351 | CTTGTTGTCACAGGT[A/G]CCCATGTTGGAGGTA | 73469 |
rs33006804 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf38 | Mm_Celera | 4:44216358 | GATGACCCCAATATG[C/T]TACTTCATAACTGTA | 73469 |
rs33026763 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44131980 | GTCTGAGGGTTCCTG[A/G]CTGGCCTATCTAGGA | 73469 |
rs33035192 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf38 | Mm_Celera | 4:44153261 | CGACAATTCTTTTCT[A/G]AGTGTCACAGCACTT | 73469 |
rs46344205 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44146728 | CATTTAATTTTTATC[G/T]TAATGAAGTCCACTT | 73469 |
rs46351214 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44195359 | ACATGTAAACTTTTT[A/T]AAAAAATCATTAACA | 73469 |
rs46370826 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44208093 | TGAGGGGAGTTGACC[A/G]GAGCGAGCAGAGGTC | 73469 |
rs46457071 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44197020 | TCTTTCCAGTGATGG[C/T]CGACTATGCCATCTT | 73469 |
rs46580530 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44223887 | CTCACAGGTGTGATA[C/T]ATTCATACACACATA | 73469 |
rs46942769 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44197099 | CATAATGTTGTTCCA[C/T]CGATAGATAGGGTTA | 73469 |
rs47016583 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44166563 | AAATACAATTCTTTC[C/T]TAACTTACAGAGAAT | 73469 |
rs47067253 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44197027 | AGTGATGGTCGACTA[G/T]GCCATCTTTTGATAC | 73469 |
rs47171301 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44146795 | GAAATCTTTGCTGGG[A/C]CTGAGAGAAAGCTGA | 73469 |
rs47202593 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44138392 | CTTTTTAGACCAACC[A/T]GGCCTTTCTAAGTTA | 73469 |
rs47227344 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44167008 | GTTAAAGAAACTTCG[A/T]TAAGTAAATGTTACT | 73469 |
rs47235990 | snp | A/C | | | upstream-variant-2KB, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44222825 | GAGTAGTGGATATTA[A/C]GAGTTTATACCTGGG | 73469 |
rs47273588 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44194060 | GTTCCCAGCATACAA[C/T]TGCCTATGCTCCAGG | 73469 |
rs47555723 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44167089 | GAGTCATGTATGAGC[C/G]CTGAATACATTTCAA | 73469 |
rs47569739 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44217845 | AGGACTTATGATACG[A/G]CATGTCCAAAACTCT | 73469 |
rs47633479 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44178415 | CATCTTCATCTGAAG[A/G]CTGCTAGAAGAAACC | 73469 |
rs47638312 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44207624 | ACCCAGTCCTACAAG[C/T]CCACTCTGACCTCTA | 73469 |
rs47670423 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44232508 | ATCCCCTCGCCTTTT[A/C]TAAGATGCACGCAGA | 73469 |
rs47845548 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44211293 | GTGAGCAGACACCAT[A/G]ACCAAGGCAAGTCTT | 73469 |
rs48153960 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44139464 | AGGAAAGGGTTTATT[C/T]GGCTTACACTTCCAT | 73469 |
rs48325539 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44167144 | ATCGCTATCCAACGA[C/T]TATATTTAAGTATTC | 73469 |
rs48673950 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44175464 | CTGCTGGAAAGACAA[C/T]CCTCAGGGCAGAGTT | 73469 |
rs48806874 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44228819 | CTATGCCTGTACTCA[A/G]AAGCTGGCGGCATGG | 73469 |
rs48883359 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44199122 | CGCATGTGCATTTGC[A/G]CACGTGTACACACAC | 73469 |
rs48888824 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44215279 | GGTTTTTTGTTTTTT[G/T]GGGGGGGGGTTTTGC | 73469 |
rs48988182 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44214960 | TGGACTACCTAGCAA[A/G]ACTTTATCTCAAAAA | 73469 |
rs49091771 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44191396 | TAGTAACACATGCAG[A/G]GCATGTGCATAAGCA | 73469 |
rs49548848 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44215000 | CGGGGTTGAGGGAAT[A/G]GCTCAGGGTTGAGGA | 73469 |
rs49727317 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44176777 | GATTTCTTGTCCCAA[C/T]AGTCTTATAAATAAG | 73469 |
rs49795971 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44208144 | TAAAAATTCAATGCC[C/T]AACAACCACATGAAG | 73469 |
rs50058367 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44192605 | CCTTAAATACTAGTT[A/T]AAAAAACCGGGCGTG | 73469 |
rs50446390 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44189972 | GTAACCCTAGCACTG[A/G]GGGACAGAAACGGAT | 73469 |
rs50844944 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44147883 | GAAGTACATACTTCA[A/T]CTACCTAGAAAGCCT | 73469 |
rs50907583 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44137966 | TGCTGGCCCCAACTT[A/G]GTTTTTGTTGGTTGT | 73469 |
rs50960585 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44178414 | ATCTTCATCTGAAGA[C/T]TGCTAGAAGAAACCT | 73469 |
rs50991733 | snp | A/G | | | intron-variant | Rnf38 | GRCm38.p3 | 4:44174396 | GAGGGGATTAGGGTG[A/G]AGTAAGGGTTGGAAG | 73469 |
rs51566983 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44207363 | TTGTTTGTTTTGAGA[C/T]ATGATTTCTCTGCAT | 73469 |
rs51633481 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44178433 | TAGGAGCTGAAAGTT[C/T]TACATCTTCATCTGA | 73469 |
rs51949650 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44167203 | CAACTTTTACTGAAT[A/G]GCCTCTAACACAAAA | 73469 |
rs52068546 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44196958 | TTTTTTGGCCCTGGC[A/G]TTCCCCTGTACTGGG | 73469 |
rs52096273 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44192073 | CAGAGGAGCAGAGGG[A/G]CAGAGGCAGAGGCAA | 73469 |
rs52338733 | snp | A/G | | | upstream-variant-2KB, intron-variant | Mir5106, Rnf38 | GRCm38.p3 | 4:44222684 | AAGAAAGAAAGAAAG[A/G]AAGGAAGGAAGGAAG | 73469 |
rs52460172 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44157492 | ttgttttTGGGATAA[A/G]GCtatatacatacat | 73469 |
rs52461161 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44157609 | acacacacacacaca[C/T]agccttggcagttcc | 73469 |
rs52520455 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44203802 | GGGCAGCCAGGGCTA[C/T]ACACACACACACACA | 73469 |
rs52534439 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44192114 | ATGAGTTTGAAACCA[C/T]CCTAGTTTAAACAGT | 73469 |
rs52574973 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44197496 | aaacaaaacaaaaaa[A/C]caccttcaatcaaat | 73469 |
rs108453578 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44206618 | TAAGGACAGCCTAAG[A/G]CTGTCTATAAGTGAC | 73469 |
rs108828558 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44178396 | CTAAGAGAATACTGG[C/T]TTTCAGGCAGCTAGG | 73469 |
rs211697433 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44132933 | GGCTACACAGACAAA[C/T]TCTGTCTCAGGAAAG | 73469 |
rs211717819 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44145045 | TGGAACTGGAGTACA[A/G]TGTGAAACTCACAAT | 73469 |
rs211735396 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44202359 | AGTTCATAAAAGCAA[A/G]AAAAAATGTTCAACA | 73469 |
rs211770994 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44201330 | AATTATAGGTGCACA[A/C]CATCATTCCTATTGA | 73469 |
rs211775658 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44210558 | CATCTTCAGCTGTTT[A/G]TGGAGTTCAGGACAG | 73469 |
rs211793111 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44193804 | ACGCCTTTAATCCCA[A/G]CACTCGGGAGGCAGA | 73469 |
rs211797644 | in-del | -/TG | | | intron-variant | Rnf38 | Mm_Celera | 4:44228420 | CACTATAATGAGTAT[-/TG]TGTGTGTGTGTGGTA | 73469 |
rs211876737 | in-del | -/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44207256 | AACTCAGATACAGAG[-/C]CTTTTGTTTCCCCAG | 73469 |
rs211925674 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44166023 | GAACTAAAGATAAAC[A/G]TCTTGACTAACAGTC | 73469 |
rs211955828 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44175123 | GCGTGTAGTAGAAAA[A/G]GGCAGTGTTCATTCA | 73469 |
rs211967271 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44165224 | GCTCCTGTGGTAAAC[C/T]GAGCAACAGACAGGA | 73469 |
rs211984360 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44226520 | CAGCACAAGTGAAAG[A/C]AGAACTATAATTCCA | 73469 |
rs212053361 | in-del | -/AT | | | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44128077 | ACCTATTTTTAAAAA[-/AT]ATATATATACACACA | 73469 |
rs212076587 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44188355 | TGAGTCAGGCACCCC[C/T]ACAATGGAAGGAGAG | 73469 |
rs212083188 | in-del | -/AG | | | intron-variant | Rnf38 | Mm_Celera | 4:44136064 | GCTGAGCAGCCAGCC[-/AG]ACTCCGAGAGAGCTA | 73469 |
rs212093099 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44155991 | CCATATGTAAACGTT[A/T]ACAATATAAATAGTT | 73469 |
rs212115556 | in-del | -/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44189632 | TAGTAAGAGCCTATC[-/T]CTATAAAATGAAATG | 73469 |
rs212156969 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44210207 | CCCTCTGAGCGCCAC[A/G]TGTTGTGTGGCATGT | 73469 |
rs212186879 | in-del | -/TTTA | | | intron-variant | Rnf38 | Mm_Celera | 4:44171749 | TTTAGATTCTTAGCC[-/TTTA]TTTATTTATTTAGGT | 73469 |
rs212187871 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44192353 | AAGCACTTAAGGGCA[C/T]ATCTGATGACGGGAA | 73469 |
rs212220564 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44217461 | CTAAAATCCCCACAC[A/T]AAAATATCTATTCTT | 73469 |
rs212245367 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44225712 | ATTACTATTTACATA[C/T]AATTTCTTCAAATTT | 73469 |
rs212276627 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44157965 | AAAAAACAAAAAAAC[-/A]AAAAAACAAACAAAC | 73469 |
rs212287903 | in-del | -/G | | | upstream-variant-2KB, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44223142 | ACAGAATGATTAGAA[-/G]TTCAAAGTCGGGGCT | 73469 |
rs212328526 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44183971 | TGCTTTTGTCTGCCA[C/T]GGTTCCCTGTCTGAG | 73469 |
rs212350431 | in-del | -/TT | | | intron-variant | Rnf38 | Mm_Celera | 4:44216677 | GAAAGACAGAATTCA[-/TT]TTTTTTTTCTAAGTA | 73469 |
rs212413377 | in-del | -/GAGC | | | upstream-variant-2KB, intron-variant | Rnf38 | Mm_Celera | 4:44169253 | TGTCAACCAGTACCA[-/GAGC]GAGCACCACTGCTCT | 73469 |
rs212415951 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44174463 | ACCCAATGAAGTAGC[A/T]CCAAAAAAGTACATC | 73469 |
rs212422635 | snp | C/T | | | synonymous-codon | Rnf38 | Mm_Celera | 4:44131607 | TAAGACTCTAAGAAG[C/T]TGCCTTGACTCAAAA | 73469 |
rs212430529 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44191788 | GTTAACAGTGCCAAC[C/T]TCCTTTCTCTACATC | 73469 |
rs212458281 | in-del | -/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44145200 | TTTATGTGTACGGTG[-/T]TTTTTTCCCCCTGCC | 73469 |
rs212545610 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44162790 | CCCACAATTTTTTTA[A/T]AAATTGAAACAAAAT | 73469 |
rs212547514 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44173122 | CTCATTCTCCTTTCT[A/T]TAAGTATTTTTCCAC | 73469 |
rs212552691 | in-del | -/CTT | | | intron-variant | Rnf38 | Mm_Celera | 4:44197659 | CTCACACAGAAAAAC[-/CTT]CTGGTCTCAAAACAA | 73469 |
rs212552829 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44155318 | CCACAAAAAGCACAT[-/A]AAAAAAAGCAAAGCT | 73469 |
rs212584483 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44172587 | AGGGTTGCATATTGA[A/G]AGCCTGTCTCAAAAA | 73469 |
rs212589522 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44223646 | AAGGCGCTGAGGCAG[A/G]ATGCCCACAAGTTCC | 73469 |
rs212602388 | in-del | -/AAAA | | | intron-variant | Rnf38 | Mm_Celera | 4:44194560 | AATTTTAAAATCTTT[-/AAAA]AAAAAAAAAAAAAAA | 73469 |
rs212602461 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44153182 | TCTACCATTCTTGTC[A/G]TCTGGGCAGTTATTT | 73469 |
rs212646428 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44208102 | TTGACCGGAGCAAAC[A/T]GGGTGGACTGGATGG | 73469 |
rs212649275 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44151838 | TCCCCTGCTCAGACA[C/T]TGGTTGATCAGCTTT | 73469 |
rs212662283 | in-del | -/TAAGACACAAC | | | intron-variant | Rnf38 | Mm_Celera | 4:44165567 | TCCATAGCACAATGG[-/TAAGACACAAC]TAAGACACAACTAAG | 73469 |
rs212664488 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44224498 | GGTTTTCTCTTCTGT[A/G]TCCCACAGCCCTTTC | 73469 |
rs212678565 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44183017 | GCTAAGAAATATCTC[-/A]AAAATTCCCAAATAT | 73469 |
rs212685095 | in-del | -/GA | | | intron-variant | Rnf38 | Mm_Celera | 4:44212733 | CCACACAGTGCTCAT[-/GA]GAGGCTTCTCTGGAT | 73469 |
rs212691286 | in-del | -/GGAT | | | intron-variant | Rnf38 | Mm_Celera | 4:44214443 | CTAAGATGACTTCTG[-/GGAT]GGATGAAATAGCTTA | 73469 |
rs212701022 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44180802 | TCTTTAATTCGTGCA[A/C]TTGAGAGGCTGACTT | 73469 |
rs212711579 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44163401 | CCAACAGGAAGCAAA[C/T]CAGGACAGTCTCTCT | 73469 |
rs212736855 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44190113 | TGGCTCCAAACACAC[C/G]GGTATGGGCAATGTC | 73469 |
rs212753660 | in-del | -/ACAT | | | intron-variant | Rnf38 | Mm_Celera | 4:44157607 | CACACACACACACAC[-/ACAT]ACAGCCTTGGCAGTT | 73469 |
rs212775035 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44198300 | GGTTAACTCTTTTTG[C/T]GGGCTTGTTGGTTTG | 73469 |
rs212806241 | in-del | -/AAACAAAC | | | intron-variant | Rnf38 | Mm_Celera | 4:44219097 | AGAAACCCTGTCTCG[-/AAACAAAC]AAACAAACAAACAAA | 73469 |
rs212859871 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44137244 | CCATAGGTACTGTAT[A/G]CACACGATATACATA | 73469 |
rs212890165 | in-del | -/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44183123 | CAAGTGACAATGAGA[-/G]GGAGTGTGCGGAGGG | 73469 |
rs212913348 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44148252 | TCCAGCTGTGACTTC[A/G]GGTTCAGGAGACTGG | 73469 |
rs212913676 | in-del | -/ACAC | | | intron-variant | Rnf38 | Mm_Celera | 4:44199129 | CATTTGCGCACGTGT[-/ACAC]ACACACACACCATAT | 73469 |
rs212956713 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44161599 | TCAACAATCGTGGTC[A/G]GTTTTACAAATCTCA | 73469 |
rs212959895 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44215885 | CCATGTGGTTGCTGA[C/G]ATTTGAACTCAGGAC | 73469 |
rs212974754 | in-del | -/AATGTA | | | intron-variant | Rnf38 | Mm_Celera | 4:44162603 | ATACAACAGAAAGCT[-/AATGTA]ACATACTACATCTAA | 73469 |
rs213017869 | snp | C/T | | | intron-variant | Rnf38 | GRCm38.p3 | 4:44197677 | CTGGTCTCAAAACAA[C/T]AACAACAAAAACAAG | 73469 |
rs213061719 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44206192 | AAGTGTCACTGCAGG[A/T]AGTAACAATGATACA | 73469 |
rs213084356 | in-del | -/ATGCTGAG | | | intron-variant | Rnf38 | Mm_Celera | 4:44201315 | CTTTTTCTTCCCCAA[-/ATGCTGAG]ATTATAGGTGCACAC | 73469 |
rs213096312 | snp | A/C | | | intron-variant | Rnf38 | GRCm38.p3 | 4:44190664 | TGTCTCAAAAAAAAA[A/C]ACAAAAGCCAACCAA | 73469 |
rs213119539 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44201421 | CCTAAAAGCTGGAAT[-/A]AAAAAAATGTCCAAT | 73469 |
rs213125099 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44232796 | CCTGGAAAAAGACAC[A/T]GTATAAACAGGCCTC | 73469 |
rs213133278 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44170454 | TTACGTGAAACTCAG[C/T]GCTGGAACACACGTC | 73469 |
rs213173451 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44181493 | ACCTTCCATTTAGAA[C/T]GGCTACACCTAGAGA | 73469 |
rs213180941 | snp | A/T | | | upstream-variant-2KB, intron-variant | Rnf38 | Mm_Celera | 4:44169412 | TCACCCCCATTATGT[A/T]TCCTTCTCTTTTCTT | 73469 |
rs213194306 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44213077 | AGAGAGCTGGAGAGA[G/T]GGCCTGGCAGTTAAG | 73469 |
rs213246673 | snp | C/G | | | nc-transcript-variant, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44221262 | GCTGTTGTTGTTGCT[C/G]GAGTGTTTTTGTTTG | 73469 |
rs213291001 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44160890 | CACCAACTCTGATGG[C/T]CTGGATTAGATTCCT | 73469 |
rs213294618 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44164904 | AACATGTGCCATAAA[G/T]CTGAGATAAATTTTA | 73469 |
rs213304865 | in-del | -/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44196116 | TATAGCAATCTTTTT[-/G]GACTGAAAAACAAAT | 73469 |
rs213320952 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44153336 | AGCTAGAAAATTTAT[G/T]CAACCATGTAACTGC | 73469 |
rs213326663 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44149806 | CTTGTATGGAATCAT[A/G]GGTAGATATCTGTTG | 73469 |
rs213372346 | in-del | -/AA | | | intron-variant | Rnf38 | Mm_Celera | 4:44227114 | TGCTTAAAATTAACT[-/AA]AAAAAAAAAAAAAAA | 73469 |
rs213377953 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44215983 | GACATCATTACTGAC[A/G]GTAGCAATGCCTTTT | 73469 |
rs213387940 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44225592 | GCACTCCTATCCAGT[G/T]AAGGAAACAAGAAAG | 73469 |
rs213405258 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44213933 | CCCCCCAATCTCTGC[C/T]TCCCAAGCACAGGCA | 73469 |
rs213430486 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44143417 | ACTTTTAACTAGTTA[A/C]AATCAAATGAGAATA | 73469 |
rs213449857 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44216454 | GGTCTTCACCCCCCC[A/C]ACCCACAGGCTCACC | 73469 |
rs213484755 | snp | A/G | | | synonymous-codon | Rnf38 | Mm_Celera | 4:44142349 | TGGTGGTGGCAAGTG[A/G]GGAGGATGATGGGGA | 73469 |
rs213489069 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44208194 | GATACAGTAGACTCA[A/G]ATACATAAAATACAT | 73469 |
rs213512337 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44182364 | AGTATGGATCCTGAT[A/G]ACTAAGAGGGAAATA | 73469 |
rs213515627 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44138054 | ACCAGGCTAGTGTCC[A/C]ACTCAGAGCTCCATC | 73469 |
rs213542623 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44181624 | AATTAGCAATGAAAA[A/G]AATGCTATCTGCCAA | 73469 |
rs213591904 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44172635 | ATTTGTCCTAATACT[G/T]AAGAAATTCATATGG | 73469 |
rs213605333 | in-del | -/AA | | | intron-variant | Rnf38 | Mm_Celera | 4:44159641 | CTTGTCTCAAGATTT[-/AA]AAAAAAAAAAAAAAA | 73469 |
rs213615812 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44179545 | TAAAAAGCCTCTGAG[A/G]CAATGTATTTAACAG | 73469 |
rs213682764 | snp | A/G | | | upstream-variant-2KB, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44222005 | TTTATGCATTTGAGT[A/G]GTGTGTCTGCATGTA | 73469 |
rs213734299 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44151354 | AGTACCACACTCCTT[C/T]CACAAGATGAACTTT | 73469 |
rs213780330 | snp | A/C | | | intron-variant | Rnf38 | GRCm38.p3 | 4:44190688 | CAACCAACCAAACAA[A/C]CAAACAAAAGAATAT | 73469 |
rs213820671 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44163642 | TAAAAAACTGTTAGG[C/T]ATAATTTCACTGATT | 73469 |
rs213830152 | snp | C/T | | | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44127208 | TGAATCCTAAATTGC[C/T]AACCACCTCTTTTAA | 73469 |
rs213843819 | in-del | -/AA | | | intron-variant | Rnf38 | Mm_Celera | 4:44172377 | GGTATGCTGGATGGC[-/AA]AAAAAAAAAAAAATT | 73469 |
rs213864368 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44197484 | AAAGGAAAGGAAAAC[-/A]AAAACAAAAAACCAC | 73469 |
rs213880254 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44161810 | GTCAGAAACTCCATT[C/T]ATCTCTAAAGACAAA | 73469 |
rs213886636 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44209012 | GAGCCCCAAATACCA[A/C]TAAGTAAATCCAGAA | 73469 |
rs213895843 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44197943 | TTGGTACTTTGAAAA[A/G]TATGATTGACAAACC | 73469 |
rs213917269 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44161066 | GATATTCACGCACTA[C/T]AAAGCAGGAAATACT | 73469 |
rs213922201 | in-del | -/CACG | | | intron-variant | Rnf38 | Mm_Celera | 4:44179836 | GACAGTGCCAGATCC[-/CACG]CACGGGCTTAGGGCT | 73469 |
rs213951645 | snp | C/T | | | upstream-variant-2KB, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44222206 | TAGCCAGGGGACTCT[C/T]GCCAGCGTGGGAACC | 73469 |
rs213965870 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44215059 | GCATAAGGACCCAAA[G/T]TTAGATCCCTAGCAG | 73469 |
rs213987854 | in-del | -/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44133182 | AAATACCCTAACCTG[-/C]CCCCCCCCCACAAAA | 73469 |
rs213998653 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44214295 | TGTCTTCTAACTCAG[A/G]TGCACACACATACAC | 73469 |
rs214017822 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44149889 | TTTGTTCTGCCATGA[A/G]TGAAGAGTATGATTC | 73469 |
rs214096372 | in-del | -/CTA | | | intron-variant | Rnf38 | Mm_Celera | 4:44178595 | CCCTAACTAAGACCC[-/CTA]GTTTGTTTGTTTGTT | 73469 |
rs214102627 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44189091 | GTGTCTTGCTCCCAC[A/C]TTGATGATAATGGAC | 73469 |
rs214167589 | snp | A/G | | | upstream-variant-2KB, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44221481 | CTGCCAGCAGTATTT[A/G]TGCAGAAATAGGTTT | 73469 |
rs214223304 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44206286 | TTGCTCCAAGGCAGG[C/T]TTATAGGCACAGTGG | 73469 |
rs214224639 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44173417 | CAGGCTGTGGCTGTT[C/G]CAACTGTGCAAGTGA | 73469 |
rs214238100 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44139085 | TAATACCCTGATCAA[C/G]AGAGATTTCCAGACA | 73469 |
rs214240003 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44174935 | TCTAATGATAAATTT[-/A]TTTAAAAAAGAAGAA | 73469 |
rs214270081 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44196142 | CAAATCCATCCACAA[A/G]CCCACAGGAAAGAAC | 73469 |
rs214273803 | in-del | -/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44138378 | CAGCCAGAACCTTGC[-/T]TTTTAGACCAACCAG | 73469 |
rs214288912 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44147202 | TAATAAAACTGCAGG[C/T]GCACCACACATCTGG | 73469 |
rs214289257 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44198360 | AACCTTGGCTGTCCT[C/G]AAGCTCTCTTGTCGA | 73469 |
rs214322128 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44207299 | ACATTTTTCACAATA[C/T]TTATTTTGGTAACCA | 73469 |
rs214332207 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44196737 | AATATCCAACTAATC[C/G]ACACATCGCTCTAAC | 73469 |
rs214363467 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44179632 | ACACTTTTTCCCTGG[A/G]CTTTTATCATTTCCT | 73469 |
rs214417080 | in-del | -/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44175860 | CATCACAACACTGCA[-/G]GGGGTCCTGTATCAC | 73469 |
rs214452959 | snp | C/G | | | synonymous-codon | Rnf38 | Mm_Celera | 4:44129606 | TGGTCACTCTGAATC[C/G]CGATGCACTTCTGAA | 73469 |
rs214464726 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44159116 | ACATGGAGAACAAGC[C/T]TATGAAGGAGAGCTG | 73469 |
rs214481922 | in-del | -/AAA | | | intron-variant | Rnf38 | Mm_Celera | 4:44192176 | ACCCCATCTTGGGGG[-/AAA]AAAAAAATAATAAAA | 73469 |
rs214498092 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rnf38 | Mm_Celera | 4:44168384 | GCCGGTGCGCAGCGC[C/T]CCTGCGCAGCCCCGC | 73469 |
rs214513903 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44231445 | GTAACTGGACTTCCA[A/G]AGTTTCTGACACTCT | 73469 |
rs214514036 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44219315 | GTCTGTGCTTTAAAG[G/T]ATTAATTATCAGGGT | 73469 |
rs214525651 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44171366 | TAGAAATAACTTGGT[A/G]GTTTAATTGTACCAA | 73469 |
rs214529409 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44232877 | GCTGACCTGGAGAGG[A/G]CCAAACGGTCCCCGA | 73469 |
rs214552984 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44170603 | GAGGTAGTCATCAAA[C/T]TGGCTTTCTTGGCAG | 73469 |
rs214564558 | snp | A/C/G | | | intron-variant | Rnf38 | GRCm38.p3 | 4:44136091 | AGCTAGAAAGGATGA[A/C/G]CTTCTTCAGCAGCGA | 73469 |
rs214572835 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44219993 | CTAGTACACTGTAGA[C/T]AGGTTTACCCAGTCA | 73469 |
rs214605046 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44211414 | GCATGGTGCAGGAGG[-/A]GCTGAGAGTTCTACA | 73469 |
rs214622295 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44159572 | TATTCAGTACTAGGG[A/C]GGCTGAGGCAAGAAC | 73469 |
rs214657264 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44204445 | ACAACAAAACAAAAC[A/C]AAAAACAGATAAATG | 73469 |
rs214658969 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44187310 | GAAACTAGTTAAGAC[A/C]CCCTGCCCTGTACTG | 73469 |
rs214694322 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44194907 | ACCAGAATGAACCAG[C/T]CCACTATTAGTAAAA | 73469 |
rs214696565 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44138093 | TTCTGCCTCAATGCT[-/A]AGAATAAAATACAAC | 73469 |
rs214745151 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44230121 | GGCCCTGGGCGTGTG[C/T]GTTCACTGTTCAATG | 73469 |
rs214774751 | in-del | -/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44137929 | CTTCCATGGCGAGCA[-/C]CCTTACCCTCTGAGT | 73469 |
rs214816703 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44218054 | ACACAAACCCTATCT[G/T]GAAGGAGGAGGAGGA | 73469 |
rs214822764 | in-del | -/CA | | | intron-variant | Rnf38 | Mm_Celera | 4:44214576 | ATTTGCTCATAGAGT[-/CA]CACACACACACACAC | 73469 |
rs214853537 | snp | A/G | | | upstream-variant-2KB | Rnf38 | Mm_Celera | 4:44234178 | GGCCGCGGGCCTCGG[A/G]GGCCAGGCCGACCGC | 73469 |
rs214859161 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44171474 | CCATTCAGGTCTTAT[A/G]ATTGTTCTTTTTAAA | 73469 |
rs214897558 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44180787 | GGTAGCAGGAGACAC[C/T]CTTTAATTCGTGCAC | 73469 |
rs214913429 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44212200 | ATCTGAAGATAGCTA[C/G]AGTGTACTTAGATAT | 73469 |
rs214984378 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44205099 | TTATTCAGATCACAT[C/G]GGAACAAGGGTAAAT | 73469 |
rs215000053 | in-del | -/TATATG | | | intron-variant | Rnf38 | Mm_Celera | 4:44207050 | AAAAAGGTTTTGTTT[-/TATATG]TATACACACACACAC | 73469 |
rs215000142 | in-del | -/AATTCAAAATGTAAGCATGC | | | intron-variant | Rnf38 | Mm_Celera | 4:44163574 | CCACCATTAGTCTGT[-/AATTCAAAATGTAAGCATGC]TTCCAGTTAATTAAA | 73469 |
rs215013738 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44172365 | TACCCATGTTGGAGG[A/T]ATGCTGGATGGCAAA | 73469 |
rs215044040 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44137977 | ACTTAGTTTTTGTTG[G/T]TTGTTTGTTATGTCT | 73469 |
rs215048798 | in-del | -/AAA | | | intron-variant | Rnf38 | Mm_Celera | 4:44194561 | AATTTTAAAATCTTT[-/AAA]AAAAAAAAAAAAACT | 73469 |
rs215088067 | snp | C/T | | | downstream-variant-500B | Rnf38 | Mm_Celera | 4:44126021 | ATGCACATACCCATG[C/T]GTGGCTACATTTTCT | 73469 |
rs215145322 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44177585 | ACTTAAAACACAATC[G/T]AAGTCGGGCGGTGAT | 73469 |
rs215147174 | in-del | -/AA | | | intron-variant | Rnf38 | Mm_Celera | 4:44160393 | TAATAAATAAATCTT[-/AA]AAAAAAAAAAAGAAA | 73469 |
rs215163415 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44136986 | CGAAATTCAGAGTAA[A/G]GAGAACAGACATCCC | 73469 |
rs215227008 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44147507 | TTATTTAAGAAAGCC[C/T]TTCTTCCTGAAGGGA | 73469 |
rs215243901 | snp | C/T | | | upstream-variant-2KB | Rnf38 | Mm_Celera | 4:44234237 | GGGCGGTGTCTGCGC[C/T]GGGGAGTGTACCCCG | 73469 |
rs215253082 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44210656 | AACCCTAGCTCTGAG[C/T]CAGGGACAATAGCTG | 73469 |
rs215265180 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44185771 | TGAGGCCAACAAGAG[-/A]AACAATTACAGCTCA | 73469 |
rs215303548 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44212320 | CACTGAGCCCCACCC[C/T]GCCCTGTGACCATGT | 73469 |
rs215326609 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44205174 | TCACCAAGAAACGCC[A/G]TTCATTCTCTACAAA | 73469 |
rs215344119 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44137187 | GTGGCTCACAACCAT[C/T]TGTAACTCCAGGTCC | 73469 |
rs215369642 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44211375 | CACTATCATCAAGGT[A/G]GGAGCATGGCAACAT | 73469 |
rs215383976 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44148199 | TACTGAAGAGGACCC[C/T]GGTTTGATTCTGGCA | 73469 |
rs215426540 | in-del | -/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44175905 | CCTGCTCAGTGAGCC[-/G]ACAGTAGCTCCTGCC | 73469 |
rs215428023 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44178481 | GGATGCTGCCATGCT[C/T]CCACCTTGATGATAA | 73469 |
rs215429717 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44146447 | CAACTGATTCTTATG[A/G]ACATCCTACATAACT | 73469 |
rs215430274 | snp | C/T | | | upstream-variant-2KB, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44222316 | CAGCTCTTCCGCAGC[C/T]GTATCCAGCGTGGGA | 73469 |
rs215434026 | in-del | -/AG | | | intron-variant | Rnf38 | Mm_Celera | 4:44159196 | CTTTAAACACAAAAT[-/AG]ACAGGCTGCACGAAC | 73469 |
rs215461272 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44177746 | AAAACAAAACAAAAA[A/C]AAAAACAAAAACAAA | 73469 |
rs215462106 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44161955 | GAATATATGATAAGC[A/T]GACTTCCTATATAAC | 73469 |
rs215466943 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44176254 | GCTAGTTTTATGACA[C/T]AAACTAGAGTCATTT | 73469 |
rs215493716 | snp | A/G | | | downstream-variant-500B | Rnf38 | Mm_Celera | 4:44126085 | CCTTCTGTGAGTCTG[A/G]GTTGTTTACCGTCAG | 73469 |
rs215512084 | in-del | -/TTTGGT | | | intron-variant | Rnf38 | Mm_Celera | 4:44198062 | TTAAGGTTTTTTTTG[-/TTTGGT]TTTTTGTTTTTTTGA | 73469 |
rs215524264 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44189218 | AAGACAGTAGGCAAA[A/T]GTCACTCAAGCATGA | 73469 |
rs215575656 | in-del | -/AAG | | | intron-variant | Rnf38 | Mm_Celera | 4:44157974 | AAAAACAAAAAACAA[-/AAG]ACAAACAAACAACAA | 73469 |
rs215584148 | in-del | -/A | | | intron-variant | Rnf38 | GRCm38.p3 | 4:44191000 | AAATAAATAAATCTT[-/A]AAAAAAAAAAAAAAA | 73469 |
rs215597209 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44186986 | GCATGCAATACCCCC[A/C]CACACACACACATAC | 73469 |
rs215608205 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44196920 | CCCCACCCCACCCCC[A/G]CTCCCCTACCCACCC | 73469 |
rs215646384 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44187407 | CAGTACAATAAGGGT[A/G]GCATGCATTTCCACG | 73469 |
rs215756640 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44157055 | TGCCAACAGCTTTGG[A/G]AAAAAAAAAAGCAAA | 73469 |
rs215781891 | in-del | -/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44170478 | CACGTCTAACATGTT[-/C]AAGGCCTTGAGCTGG | 73469 |
rs215794867 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44156398 | TACATGCCCACACAC[A/G]TGCACACAATCATTT | 73469 |
rs215814278 | in-del | -/AAAAA | | | intron-variant | Rnf38 | Mm_Celera | 4:44145908 | TCTTAAAAACAAAAC[-/AAAAA]AAAAGAGATTTATTT | 73469 |
rs215826616 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44159754 | GGAAATGAAGACAAA[C/T]TCCTAAGTCTGAAAG | 73469 |
rs215857241 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44218195 | GACTTCATATTCTTG[C/G]TAGGTTTAGTAGTGC | 73469 |
rs215858866 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44223448 | TTTTAAAGAAAATAC[C/T]TGATTGATTACTTTA | 73469 |
rs215871350 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44211304 | CCATGACCAAGGCAA[C/G]TCTTATAAAGGACAA | 73469 |
rs215872842 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44145940 | TCATTTGAATGAACG[C/T]GTAATGTGTGTGTCT | 73469 |
rs215901928 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44210600 | GAGGACCCTGTCCTG[A/G]ATGGATGGACAGACG | 73469 |
rs215910484 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44145223 | CCCCTGCCTGTAGAT[C/T]ATGTAATCAGAGTGC | 73469 |
rs215914800 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44219011 | CACTCGGGAGGCAGA[A/G]GCAGGCAGATTTCTG | 73469 |
rs215916630 | snp | A/G | | | upstream-variant-2KB | Rnf38 | Mm_Celera | 4:44235599 | ACTGAAACACAGTGA[A/G]ATTATCTTTGACCAA | 73469 |
rs215925656 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44207060 | TGTTTTATATGTATA[C/T]ACACACACACACACA | 73469 |
rs215981792 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44185620 | CTCACATGCTCATTT[C/T]TAAACTGTGGCATAT | 73469 |
rs215990938 | in-del | -/AAAA | | | intron-variant | Rnf38 | Mm_Celera | 4:44149416 | TTCCAAATTAACTGT[-/AAAA]AAAAAAAAAAAAAGC | 73469 |
rs216003931 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44197537 | ACACAGAACAGCAGG[A/G]CATCATGACAGGAGT | 73469 |
rs216067140 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44217620 | AGTTTGCATACACAG[C/T]CAAACAAGCATTTGG | 73469 |
rs216157094 | snp | A/C | | | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44127044 | CTACAAAGATGCTCA[A/C]GGAGGCCATGGAGAC | 73469 |
rs216162294 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44144313 | TCTCTATATAGCCCT[A/G]GCTATCCTGGAACTC | 73469 |
rs216177141 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44192361 | AAGGGCACATCTGAT[G/T]ACGGGAACTGACCTG | 73469 |
rs216186782 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44231599 | GAGGTAGGTGGATCT[A/G]TGAGTTCGATGCCAG | 73469 |
rs216216580 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44160853 | CGGTCAACAAGATGG[C/T]TCAGTAGGTAAAAGG | 73469 |
rs216220937 | snp | G/T | | | upstream-variant-2KB, intron-variant | Rnf38 | Mm_Celera | 4:44169104 | AATCAAACCTCTAGA[G/T]GGCTTAACCCTTCCC | 73469 |
rs216232853 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44184156 | CATGGAAAGGTTGGA[A/T]AGCCCCAATTCCACA | 73469 |
rs216232934 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44192939 | CAGCGCTATGACGGG[C/T]GGATACTCGCCTAGG | 73469 |
rs216258630 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44135176 | ACACAGCTCAGCAGG[C/T]AGGGGAGAGCCGTCA | 73469 |
rs216260167 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44170399 | CCTTGAAGTTTTTAA[C/G]TATAGCTACAGGTTT | 73469 |
rs216260572 | in-del | -/AAAC | | | intron-variant | Rnf38 | Mm_Celera | 4:44197716 | AAAACAAAAAAAAAA[-/AAAC]AAAAAAACACACACA | 73469 |
rs216271425 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44212233 | TAATAAATAAATCTT[-/A]AAAAAAAAAACAATT | 73469 |
rs216305210 | snp | C/T | | | nc-transcript-variant, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44221230 | GACCTAGGCCCTAGA[C/T]AGGCTCTCGGGTTGT | 73469 |
rs216381540 | in-del | -/CTAT | | | intron-variant | Rnf38 | Mm_Celera | 4:44131985 | GGGTTCCTGGCTGGC[-/CTAT]CTATCTAGGAGGAAA | 73469 |
rs216387175 | in-del | -/ACACAC | | | intron-variant | Rnf38 | Mm_Celera | 4:44203803 | GGCAGCCAGGGCTAT[-/ACACAC]ACACACACACACACA | 73469 |
rs216398453 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44196038 | AAAGAAAAATAAAAA[C/G]TTTCCATGATAAAAA | 73469 |
rs216403532 | in-del | -/TTTGT | | | intron-variant | Rnf38 | Mm_Celera | 4:44157461 | TTCCAGTTTTGTTTC[-/TTTGT]TTTGTTTTGTTTTGT | 73469 |
rs216455365 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44231733 | AAACACATACATACA[C/T]ACATACATACACACA | 73469 |
rs216455472 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44230184 | CTGCTCATGTGGATG[A/C]GAGAGGCAGTTTAGG | 73469 |
rs216539645 | in-del | -/GA | | | intron-variant | Rnf38 | Mm_Celera | 4:44205608 | TATCTTGGGGGGGGG[-/GA]TGCCCCTTTAATTCC | 73469 |
rs216545699 | in-del | -/TGGCCACCC | | | intron-variant | Rnf38 | Mm_Celera | 4:44189600 | GAACCTACACGTTTG[-/TGGCCACCC]TGGCCAAGTTAGTAA | 73469 |
rs216596561 | in-del | -/TT | | | intron-variant | Rnf38 | Mm_Celera | 4:44223514 | GGTTTTTTGCTTTTG[-/TT]TTTTTGTTTTTTTTT | 73469 |
rs216608965 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44232630 | ACTTCCTTCCCCCTT[C/T]TAGGACAGCTGCTCT | 73469 |
rs216624556 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44204396 | GGACTATGCAGAGTG[A/C]CAAGTCAGGACTGCA | 73469 |
rs216625536 | in-del | -/CC | | | intron-variant | Rnf38 | Mm_Celera | 4:44213913 | CCCAATGCAGCACAG[-/CC]CCCCCCCCCCAATCT | 73469 |
rs216648922 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44136019 | TTTGACTCAGCCAGC[A/T]TGGAGAGGAGTCTGA | 73469 |
rs216658592 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44203533 | GTGCCACATGTAGAG[G/T]TCTGAAGACAACTTG | 73469 |
rs216701432 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44135228 | CCATGCCTAGAACCT[G/T]TGTGATGATGAGAGA | 73469 |
rs216707350 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44222975 | CATACACAATATTTT[-/AA]AAAAAAAAAAGTTTA | 73469 |
rs216722548 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44177527 | ACCACTGGCGATACA[A/G]TAAAACTAATGATGC | 73469 |
rs216723847 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44167142 | AAATCGCTATCCAAC[A/G]ATTATATTTAAGTAT | 73469 |
rs216730817 | in-del | -/AGCTAGAC | | | intron-variant | Rnf38 | Mm_Celera | 4:44135881 | TACAGAGAAAGAACA[-/AGCTAGAC]ACAGGTGATAATAGA | 73469 |
rs216760661 | in-del | -/ACT | | | intron-variant | Rnf38 | Mm_Celera | 4:44230743 | CTAGCTATTTGTTAC[-/ACT]ACTACTACTACTCTC | 73469 |
rs216814875 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44194106 | TGGTCTCTGTGGGTA[C/T]CTCCACACACATGGC | 73469 |
rs216840635 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44195981 | TCTGACTGGACTGCC[A/G]ACCCAGACCATTATC | 73469 |
rs216853377 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44229821 | TACATTACTATGTAT[A/G]TATATAACCACAAAT | 73469 |
rs216873529 | snp | C/G | | | intron-variant, upstream-variant-2KB | Rnf38 | Mm_Celera | 4:44168084 | AACCGCAGAACTCGA[C/G]AGCCTCCCACCTCGG | 73469 |
rs216894437 | snp | C/T | | | synonymous-codon | Rnf38 | Mm_Celera | 4:44133744 | CTCTCCCAGTCTCTC[C/T]GCCAAGTTTAACAGG | 73469 |
rs216903980 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44228400 | GGAATAAAGGTGTGA[G/T]CCACCACTATAATGA | 73469 |
rs216958664 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44202157 | GGCATAGCTTTAATC[C/T]CAGCACTCAGGAAGT | 73469 |
rs217091634 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44202368 | AAGCAAAAAAAAATG[A/T]TCAACATCTCTAGTC | 73469 |
rs217103448 | in-del | -/AA | | | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44126687 | ATTTCAGATTCTGCT[-/AA]AAAAAAAAAAATTTC | 73469 |
rs217132081 | in-del | -/ATACACACAC | | | intron-variant | Rnf38 | Mm_Celera | 4:44203801 | AGGGCAGCCAGGGCT[-/ATACACACAC]ACACACACACACACA | 73469 |
rs217146021 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44209714 | GAGAAACCATGTCTC[A/G]AAAAAACAACCTATT | 73469 |
rs217154339 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44132812 | TTAAGAGGCTGATAG[A/G]CAGGCAGGCAGGCAG | 73469 |
rs217166241 | in-del | -/ACAA | | | intron-variant | Rnf38 | Mm_Celera | 4:44202711 | GAAACAAAAAAACTC[-/ACAA]AAAAAAAATGTCTTT | 73469 |
rs217176791 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44201159 | AGTTAACTGGGGACT[A/G]ATTCCACGGTGAACA | 73469 |
rs217183991 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44144490 | CAAGAATGGCCTTGA[A/G]TTCCTGACCCTCTGC | 73469 |
rs217190153 | in-del | -/GGG | | | intron-variant | Rnf38 | Mm_Celera | 4:44182761 | TCTTTTTCAAAAGTT[-/GGG]GGGGGGGGGGCAGAG | 73469 |
rs217213465 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44209844 | AGTAAGGTGAAAATG[A/G]AAATGTTAACCATTT | 73469 |
rs217235185 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44175272 | CTTCATACACAAATG[A/C]TAAGTTCTCTCTGTC | 73469 |
rs217245335 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44152861 | GACTGTTCTTCCAGA[A/G]GTCCTGAGTTCAATT | 73469 |
rs217280689 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44174382 | ATGTTGTGGTGTTGG[A/G]GGGGATTAGGGTGAA | 73469 |
rs217311975 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44173655 | ACAGCATCTGAGATG[G/T]AAGAGCAGAGAGACA | 73469 |
rs217312247 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44183858 | TCCCTCCCACAGCCA[G/T]ACAATTTAACAAAAC | 73469 |
rs217369536 | in-del | -/AC | | | intron-variant | Rnf38 | Mm_Celera | 4:44186486 | CTTGGGCCCAAAGTA[-/AC]ACACACACACACACA | 73469 |
rs217392029 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44226993 | CATCCACTGAGCCAC[C/T]GTGCCAGCCCTTAGT | 73469 |
rs217422016 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44166089 | ATTTTTATTTTAAAG[A/G]CTTCTCACCCACATT | 73469 |
rs217461953 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44130448 | TTGTTACTACTCAGT[A/T]TGCCTGGCTCACCCT | 73469 |
rs217491631 | in-del | -/CC | | | intron-variant | Rnf38 | Mm_Celera | 4:44213873 | GACATTCACGTCTAA[-/CC]CCCCACCCCCGCAGG | 73469 |
rs217494941 | in-del | -/AA | | | intron-variant | Rnf38 | GRCm38.p3 | 4:44190664 | GTCTCAAAAAAAAAC[-/AA]ACAAAAGCCAACCAA | 73469 |
rs217541663 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44188313 | GTTCGGTAGTAAATA[G/T]TAAAGCTACTTGCTG | 73469 |
rs217545787 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44182570 | TGGCACCGGAAGTCA[C/T]ACTTGGTTCTACAGG | 73469 |
rs217546242 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44215162 | ACAAGGAGTGACAGA[C/G]GAAGACCCAGTGTCA | 73469 |
rs217549100 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44157938 | AAACCCTGTCTCAGG[-/A]AAAAAAAAAAACAAA | 73469 |
rs217567569 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44208032 | CTACAATGTACTTAT[A/G]TATAATAATAAATAA | 73469 |
rs217600494 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44207476 | TGGGATTAAAAGAGT[A/G]TACCACCAGTCAGTT | 73469 |
rs217601933 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44215803 | TTTATTTATATGTGT[A/G]CACTGTTGCTGTCTT | 73469 |
rs217624250 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44178527 | AACCTGTAAGCCAGC[C/T]CCAATGAAAATGTTG | 73469 |
rs217629996 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44173587 | CCCCTCCCCACCCCC[-/A]AAAAAGACTCAATCT | 73469 |
rs217763332 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44141948 | TACAGAATGCACACA[C/G]GGAAGAACAGACTTA | 73469 |
rs217763519 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44129710 | CTCATGCAGTGAAGC[A/G]CCCAGTTCTCCTGTT | 73469 |
rs217772710 | in-del | -/CAGTCTAAG | | | intron-variant | Rnf38 | Mm_Celera | 4:44163252 | GCAGGTTGGGCAAGA[-/CAGTCTAAG]CAGTGTAAGTACCAC | 73469 |
rs217851216 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44158856 | ACAAGCTAGAATGTA[C/T]CTGTGACTTTCAGCC | 73469 |
rs217860846 | snp | A/T | | | upstream-variant-2KB, intron-variant | Rnf38 | Mm_Celera | 4:44169638 | CTAATGTGGTGGGGC[A/T]GAAATTATGTCTTAG | 73469 |
rs217889570 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44192534 | AGAGGAACAGAGAGA[C/G]ACAGAGAGAGATAAC | 73469 |
rs217905837 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44211352 | CTTACAGGTTCAGAG[G/T]TTCAGTCCACTATCA | 73469 |
rs217994678 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44224323 | ACTATAATTACAGTG[A/G]TCCCGCCTCTCAGAA | 73469 |
rs218026846 | in-del | -/AAG | | | intron-variant | Rnf38 | Mm_Celera | 4:44203951 | GAGGAAGAGAAAAGA[-/AAG]AAGAACTTGGAGAAT | 73469 |
rs218027626 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44155063 | TCTAAACTAACACGA[G/T]GGGATAGAGCCACGC | 73469 |
rs218048201 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44195322 | ATGCTGAGATTAAAG[A/G]TGTGAAGAATCAAGT | 73469 |
rs218068039 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44153778 | CAGGTAAGCCGCCGT[A/T]CTAGCACCAACAATG | 73469 |
rs218082159 | in-del | -/AT | | | intron-variant | Rnf38 | Mm_Celera | 4:44158065 | GCTAAATACTTACAA[-/AT]ATATTTACAGAAATA | 73469 |
rs218093391 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44211974 | GAGGTAGGAGGATCC[G/T]AAGTTTAAAGTTACC | 73469 |
rs218116330 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44146930 | CTCTTCTGACCTCGG[C/T]AGGCACTAGGTATAC | 73469 |
rs218169290 | in-del | -/AACT | | | intron-variant | Rnf38 | Mm_Celera | 4:44217021 | CTCAAACATCAACAC[-/AACT]AACTCCAGGCCCCCT | 73469 |
rs218196369 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44191039 | ACTGGTCAATTCTGA[A/G]CGTGCATCTTTCTTC | 73469 |
rs218198812 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44163222 | TGGGCAAGTGGTCCT[A/G]GACTGCATTAGAAAG | 73469 |
rs218226521 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44198599 | TTAATAATGGATATT[A/G]GGGGCAATTTTTTTT | 73469 |
rs218248843 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44219171 | AATATTAAACAAAAA[A/G]TGTAAGCTGTCTCAA | 73469 |
rs218345257 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44218413 | TAGAGGCAGTGCTGC[A/G]TGCGAGCCAGGGCCT | 73469 |
rs218356554 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44129736 | CTGTTCCTCCCAGAT[A/G]GTCTTTGCATTCTAG | 73469 |
rs218375644 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44157174 | TTAAAAGTTAATATT[C/T]ATTCCTGAAACCTTC | 73469 |
rs218400040 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44162241 | GAGAAAAGGGAGCCA[C/T]AGAGCAGGGAACTGG | 73469 |
rs218421986 | snp | G/T | | | intron-variant | Rnf38 | GRCm38.p3 | 4:44193555 | CCTAACTACTGGCTG[G/T]CCTGGGTTACACATC | 73469 |
rs218436640 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44198121 | GTCCTGGAACTCACT[C/T]TGTAGATCAGGCCAG | 73469 |
rs218445905 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44184936 | GGAGGTCAGTCCAGA[C/T]GCCCTTTGGTACGTT | 73469 |
rs218493483 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44192976 | GGGACCTGGCTGCAC[A/G]GGGATACGGGGAAGG | 73469 |
rs218520854 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44186075 | CTTCCCACAGCCCAG[A/G]TTGGTTGGAACTTGC | 73469 |
rs218547905 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44170817 | AAAAAGTTTTAGTAA[C/T]TGTAAAGAAGAACAA | 73469 |
rs218551835 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | Rnf38 | Mm_Celera | 4:44232180 | TACCAAAACAAAACC[-/AAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 73469 |
rs218603954 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44171665 | AAGGACTGTAGGACC[A/G]CTGTTACACTTTCTT | 73469 |
rs218604065 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44161259 | ACCAACCCAAAAGAG[A/G]TAAGACGTATATTTG | 73469 |
rs218684901 | in-del | -/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44130267 | CTTCCCGAGTGCTGA[-/T]ATGAACAGAGTGAGG | 73469 |
rs218713423 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44233227 | GTTCTCAGCCAAGAC[A/T]CGACTCTAGCTGGCT | 73469 |
rs218732562 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44165900 | TGTAAACAGCACCAG[A/T]GACACCATGCAACAA | 73469 |
rs218742293 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44136304 | GTTTACATGGAGATA[C/T]AGAAGATTAAATAGA | 73469 |
rs218830635 | snp | A/G | | | upstream-variant-2KB, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44222449 | GACCCCATGGAAAGC[A/G]TACGGCAGTCTCCCA | 73469 |
rs218860213 | snp | C/T | | | upstream-variant-2KB | Rnf38 | Mm_Celera | 4:44234410 | AGGAAAGAAACTCTC[C/T]CTTCGCTTCTGAGGC | 73469 |
rs218883779 | in-del | -/AAAA | | | upstream-variant-2KB | Rnf38 | Mm_Celera | 4:44235308 | AAAACAAAACAAAAC[-/AAAA]AAAAAAAAACCACAC | 73469 |
rs218936545 | in-del | -/AT | | | intron-variant | Rnf38 | Mm_Celera | 4:44194718 | TCAGTTATAAAGTAC[-/AT]ATATGTATCATACAT | 73469 |
rs218958401 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44129834 | AGTCCTGAGTCAAGC[-/A]AGCCTCAGGTACGTG | 73469 |
rs218974924 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44196562 | GACAACAGCAGAACT[A/G]GTGAGAAAACATACA | 73469 |
rs219029948 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44135686 | CCAAACAATGAAAGT[A/C]TAAAGCTACTTTGTA | 73469 |
rs219032992 | in-del | -/GACA | | | intron-variant | Rnf38 | Mm_Celera | 4:44202555 | GGGCCAGCATTCAAG[-/GACA]GACAGAGATAGATGA | 73469 |
rs219040374 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44216473 | CACAGGCTCACCCCC[C/G]CAACCCACAGGCTGA | 73469 |
rs219064645 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44141453 | GGGTTAAAGGAGACT[A/G]TTTCAAAAAACTTTA | 73469 |
rs219074324 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44225639 | TTTGGATGAGGTCTA[C/T]AGTAAGATCTGTAGA | 73469 |
rs219099840 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44151877 | AATCAGAGACTAAGT[A/G]GGGAGCAGTGTTCAC | 73469 |
rs219109714 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44165013 | ATCTCCCAAACTAAT[C/T]GAATGATACAACAGT | 73469 |
rs219127141 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44226444 | CCAAACCGAGGACTG[A/G]GGATATAACTAAATT | 73469 |
rs219148332 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44191102 | CTCTCCTCCTTAAAA[C/T]TGTCACGTGGCACCT | 73469 |
rs219178750 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44191448 | TATGTTACCTGAACA[G/T]GGGTTGTTACAGGTG | 73469 |
rs219201841 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44203957 | GAGAAAAGAAAGAAG[A/G]ACTTGGAGAATGATG | 73469 |
rs219252942 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44162301 | CAGTTACCATAATCT[A/G]TCAACCAATGATTTT | 73469 |
rs219387327 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44150967 | GAGCTCTGTTCCTGG[C/T]TTGCAGATACTCTGC | 73469 |
rs219395588 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44192322 | AGAAGGATGGAGGAG[A/C]TCTCTCGGTGGGTAA | 73469 |
rs219399175 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44151689 | TCTATTCTAATGCTC[C/T]AGCCAACCTTGCTAC | 73469 |
rs219441781 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44162708 | TATAGGGCTTGGATA[C/T]CACTCAATGGTAGGG | 73469 |
rs219447152 | in-del | -/GGGC | | | intron-variant, utr-variant-5-prime, frameshift-variant, upstream-variant-2KB | Rnf38 | Mm_Celera | 4:44167484 | GTCTCGTCCAGGCAG[-/GGGC]GGGCGGGCCGGCTCC | 73469 |
rs219456410 | in-del | -/ATAAATAA | | | intron-variant | Rnf38 | Mm_Celera | 4:44214839 | AAAAACAGAAATAAC[-/ATAAATAA]ATAAATAAATAAATA | 73469 |
rs219473000 | in-del | -/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44205990 | TGTCTTTAAGTTATG[-/C]GGAGTAAAGATACTA | 73469 |
rs219493596 | in-del | -/CGCGCGCACACACACACACA | | | upstream-variant-2KB, intron-variant | Rnf38 | Mm_Celera | 4:44169753 | GCGCACACACACACG[-/CGCGCGCACACACACACACA]CACACACACACACAC | 73469 |
rs219496510 | in-del | -/AAAAC | | | intron-variant | Rnf38 | Mm_Celera | 4:44145899 | ATTAAATAGATCTTA[-/AAAAC]AAAACAAAAGAGATT | 73469 |
rs219524155 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44215288 | TTTTTTTGGGGGGGG[G/T]TTTTGCTGGGGGTTA | 73469 |
rs219556840 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44214753 | TTACCCTGTGGGTTC[C/T]CAGATCAAACTCTTG | 73469 |
rs219567802 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44223774 | GCTCTTGCTCTTGCA[A/G]AGGACGCAGGCTCTG | 73469 |
rs219621846 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44190275 | CCCCCCAACATTATC[A/G]CCTTAAATCTGAGAC | 73469 |
rs219638725 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44213138 | TTCAATTCTCAGCAC[A/C]CACATGGCAGCTCAC | 73469 |
rs219655725 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44189577 | AATGTTGAGTAAGAG[A/G]ATCACTTGAACCTAC | 73469 |
rs219688917 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44184437 | CGAGCCTCCCGAGTG[C/T]TGGGATTAAAGGCGT | 73469 |
rs219716857 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44198466 | CCAGCCTGGTCTACA[A/G]AGTTCCACGATAGCC | 73469 |
rs219748049 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44219636 | TAAAGGCGTGCGCCA[C/T]CACACCCGGCTAGTC | 73469 |
rs219748260 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44231839 | GCTTCCCACTTGCTG[C/T]GGTGACCAGCTGGCC | 73469 |
rs219767201 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44174690 | GTCTGAAGACAGCTA[C/T]AGTGTACTTATTTAT | 73469 |
rs219768415 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44148474 | CCTGAGTGCTGAATA[A/C]AGTTGCTGCAGATGG | 73469 |
rs219776691 | in-del | -/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44157980 | CAAAAAACAAACAAA[-/C]AAACAACAATCCAGT | 73469 |
rs219806645 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44147829 | TTGCTACTTCTGCTC[A/G]TGTTCTTTTTCCTCA | 73469 |
rs219828610 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44205609 | ATCTTGGGGGGGGGG[-/A]TGCCCCTTTAATTCC | 73469 |
rs219857047 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44197184 | ATGATATAGCTGTCT[C/G]TTGTGAGACTAGGCC | 73469 |
rs219865680 | in-del | -/AGG | | | intron-variant | Rnf38 | Mm_Celera | 4:44192896 | CCCCCAGAGGGCTAA[-/AGG]AGTAGAAAAAAAGAG | 73469 |
rs219873602 | in-del | -/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44171211 | GAGGGAGACAGCCAC[-/G]GGACAACCTTGTTTT | 73469 |
rs219879285 | in-del | -/ATAT | | | intron-variant | Rnf38 | Mm_Celera | 4:44150415 | CTGTTCTGTTTACGA[-/ATAT]ATATATATATAGGCA | 73469 |
rs219885068 | in-del | -/AT | | | intron-variant | Rnf38 | Mm_Celera | 4:44137509 | ACAGCGAGGGCACTC[-/AT]AAAGCAAAGCCTCTC | 73469 |
rs219889439 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44196592 | AGACGGTCCCGTCAC[A/G]CTGAGTAAGGGAACA | 73469 |
rs219893414 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44220577 | AGCCTGGCAATCTGA[A/G]TCTGATTCCCAAAAT | 73469 |
rs219935270 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44132179 | CAAGTGACAAAAAGG[A/G]ACATTTCTTCTAATT | 73469 |
rs219948746 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44187740 | TGGTTCTCCTTCTAA[C/T]GTGTGGCACCTAGGG | 73469 |
rs219952390 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44159358 | CTGAGGTAAAACACT[G/T]AAGTGGAGTGATGAA | 73469 |
rs219975385 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44195517 | GAAAACAAAACAAAG[G/T]CTGGAGAGATGTTAT | 73469 |
rs219975651 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44186866 | GATGGAAGCTGAAAT[G/T]GTCATGGAAGCACAG | 73469 |
rs219999842 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44208532 | TGGAACTCAAATATG[C/G]AGACCAGACTGGCCT | 73469 |
rs220019959 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44230630 | TTCTTACTCACTGAC[C/T]CTTTTCTCCAGCCCC | 73469 |
rs220046918 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44185067 | AAAAATGGGGCTGGC[A/G]AGATGGCTCAGTGGG | 73469 |
rs220057966 | in-del | -/AC | | | intron-variant | Rnf38 | Mm_Celera | 4:44231741 | CATACATACATACAT[-/AC]ACACACACACACACA | 73469 |
rs220074007 | in-del | -/TT | | | intron-variant | Rnf38 | Mm_Celera | 4:44215289 | TTTTTTGGGGGGGGG[-/TT]TTGCTGGGGGTTAGC | 73469 |
rs220093443 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44157363 | TCAATAGATCTGCCT[A/G]TCTCTGCCTCCCAAA | 73469 |
rs220108601 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44160135 | AAATCAATCGCTGTT[A/T]AGTAAGTTTCTGATG | 73469 |
rs220155595 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44194532 | GACAGGGACAGTGTA[C/T]TCATATAAATAAAAA | 73469 |
rs220213190 | in-del | -/AT | | | intron-variant | Rnf38 | Mm_Celera | 4:44164468 | AATTGATATAATCAA[-/AT]TTGTGACATTTCTTC | 73469 |
rs220224342 | in-del | -/AA | | | intron-variant | Rnf38 | GRCm38.p3 | 4:44207867 | ACCCATAAAATAATT[-/AA]AAAAAAAAAAAAATT | 73469 |
rs220225798 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44172795 | CCTATCCAACCGGCC[A/C]GGCCTCTGGTCCTGA | 73469 |
rs220255562 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44166596 | GAGGCCAAGATCTCT[C/T]AGAGCAGAACCTAAT | 73469 |
rs220290854 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44216577 | GACAACTCTTCTCAA[C/T]TGCCCGCGTTAACCG | 73469 |
rs220300398 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44216207 | AGCCATGAGGTCAGA[G/T]AAGTTCTTAGCTCGT | 73469 |
rs220318941 | in-del | -/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44224281 | TCTTTACCCTGCCTG[-/C]CCCCGTTACTTGCTT | 73469 |
rs220386651 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44209141 | CTGAGAGAAAAGCTC[C/T]GCGTGACTAAAACTG | 73469 |
rs220404538 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44156698 | CTACATCACAGCAGG[G/T]TTTCTAAGAGGAGAG | 73469 |
rs220406066 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44167209 | TTACTGAATGGCCTC[C/T]AACACAAAAGCGTTG | 73469 |
rs220414588 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44143700 | GGGGGAGGTAGCTCA[A/G]GTAGTAGGGTATGTA | 73469 |
rs220422609 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44212771 | AGGTGAGGCCAGCAA[A/C]GAGAGCTGTCTGTAA | 73469 |
rs220503953 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44227511 | GGTACTGTGGTAACC[C/T]CCGTGGAACCCCTGG | 73469 |
rs220508254 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44173833 | ACAGCACACATGTTG[A/G]GTACTGACTGGGGAG | 73469 |
rs220539346 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44214434 | CCAAAACTGCTAAGA[G/T]GACTTCTGGGATGGA | 73469 |
rs220539353 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44205299 | ATTATGTCACTGAAA[C/T]AAAACCTTTTTGTTT | 73469 |
rs220552377 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44182762 | CTTTTTCAAAAGTTG[C/G]GGGGGGGGGGGCAGA | 73469 |
rs220621341 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44218542 | CTCTCCATGCTCCAG[G/T]TTCTTCATCTGTACA | 73469 |
rs220641280 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44179084 | CCCCCTTCAACTACG[G/T]GCATACCCTGAGGTG | 73469 |
rs220653096 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44217668 | GCAGTAGTAGGCAGT[A/G]CACACCTTTAATCCC | 73469 |
rs220653101 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44228825 | CTGTACTCAGAAGCT[G/T]GCGGCATGGACATGG | 73469 |
rs220656092 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44150660 | CAGATATTTAAGATA[C/T]AACTTTTATTTTAAA | 73469 |
rs220672457 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44178022 | CAAGCAAATATTATT[C/T]GCCCATTAAACAATA | 73469 |
rs220674915 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44188471 | AGTATACTATTAAGT[C/T]ATATTCCTATTACTA | 73469 |
rs220728445 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44214495 | CTAGTCCCAGACCCA[G/T]GTAGAGGTGGCAGCC | 73469 |
rs220738224 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44215289 | TTTTTTGGGGGGGGG[G/T]TTTGCTGGGGGTTAG | 73469 |
rs220782435 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44135385 | TAGACTTAATAAGGT[A/G]TACGCAAGAACTATA | 73469 |
rs220802601 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44139345 | CTTATAATTTTAACA[C/T]TTGAGGTGAAGGCAG | 73469 |
rs220819309 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44190519 | GAATAATCTCAGCCG[A/G]GCGGTGATGGCACAC | 73469 |
rs220827355 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44146477 | TGATGAGCATCTGAA[C/T]CCACTCCTCAGAGTT | 73469 |
rs220840802 | in-del | -/TGCTTAGCA | | | intron-variant | Rnf38 | Mm_Celera | 4:44230987 | CTGTGACAGAGGACT[-/TGCTTAGCA]TATAGGAGGCTGGGT | 73469 |
rs220842120 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44134638 | CTTTCAAGATTCAGC[G/T]TAAACATCTTTGCTT | 73469 |
rs220857251 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44148546 | TTGCTTTCAATTATA[C/G]GTTCAAAAAACATAT | 73469 |
rs220911214 | in-del | -/AGC | | | intron-variant | Rnf38 | Mm_Celera | 4:44175637 | AAGGAGAAACTAAGG[-/AGC]AGAGCAGCACGGACG | 73469 |
rs220956184 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44136147 | GCCTAGAGAAGATTG[C/T]ACGGAGGCTGGAAGC | 73469 |
rs220965018 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44180023 | CCCACGTCAGATGCT[A/G]GCTGGCACGAGCCTC | 73469 |
rs220993976 | in-del | -/AA | | | intron-variant | Rnf38 | Mm_Celera | 4:44131816 | TGACGACACATTATC[-/AA]AAGTTTCTGGTTAAG | 73469 |
rs221009247 | in-del | -/AC | | | intron-variant | Rnf38 | Mm_Celera | 4:44197329 | CAAGCCTCGACAAAT[-/AC]ACAAGAAGCACTTGC | 73469 |
rs221125696 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44145669 | TGTTTTATATTAATA[G/T]TAGCTATTTATCTCA | 73469 |
rs221149825 | in-del | -/T | | | intron-variant | Rnf38 | GRCm38.p3 | 4:44184295 | CCTACCATGATCAAC[-/T]TTTTTTTTTTTTTTT | 73469 |
rs221161921 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44207547 | ACAGCTCACTGGATC[C/T]AGGGACTTCCCACCA | 73469 |
rs221193824 | in-del | -/GGCCCCACACAG | | | upstream-variant-2KB, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44222543 | TCCCCTGGCGCCCAC[-/GGCCCCACACAG]GACACCCAGGCCTAC | 73469 |
rs221208267 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44218664 | TAAGCACACTTTAAC[A/G]GGCCAATGTTATGTG | 73469 |
rs221307533 | in-del | -/TTTGGGGGGGGG | | | intron-variant | Rnf38 | Mm_Celera | 4:44215277 | TTGGTTTTTTGTTTT[-/TTTGGGGGGGGG]TTTTGCTGGGGGTTA | 73469 |
rs221361162 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44211502 | TTAAAGCCCACACCC[A/T]CAGTGACAAACTTAT | 73469 |
rs221363029 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44220322 | GAACTCAGGTAGGTT[C/T]TGTGAGTTCCAGTCC | 73469 |
rs221396463 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44219419 | ATATAATGATAGCCT[A/G]TTTCACCTGCCTCCA | 73469 |
rs221408234 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44211119 | GAAAGTAAGACAGTA[C/T]TCAAGTGTGGGTATA | 73469 |
rs221435311 | in-del | -/TTT | | | intron-variant | Rnf38 | Mm_Celera | 4:44170944 | TTTGATTTGCTCTAA[-/TTT]TTTTTTTTTTAAATC | 73469 |
rs221442709 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44213426 | GCTGTCTTCAGACAC[A/T]CCAGAAGAGAGCATC | 73469 |
rs221452675 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44216249 | TAACACAGTTAACAG[C/T]ATCTTCACTAAGAAC | 73469 |
rs221476531 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44186342 | CAGGCAGATGTTTAA[A/G]TTCAAGGCCATCCCT | 73469 |
rs221511737 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44185279 | GAGCGAGCAGAGGTC[A/C]TAAATTCAATTCCCA | 73469 |
rs221538741 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44176367 | AATAATGTGAGAAGG[A/G]CCCAGCCCTTTGTAG | 73469 |
rs221545093 | in-del | -/ACGAAAGGGCA | | | intron-variant | Rnf38 | Mm_Celera | 4:44145250 | GTGCCCATGGAAGCC[-/ACGAAAGGGCA]ACAGTTACCCCTACA | 73469 |
rs221545256 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44209230 | AAGTTATAGTTTAAC[G/T]GCAATAGGAAAGAAA | 73469 |
rs221564018 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44216585 | TTCTCAACTGCCCGC[A/G]TTAACCGGTCCTCAC | 73469 |
rs221579868 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44212452 | TGTATGGGTGTTTTG[A/C]ATGCATGTATGTCTT | 73469 |
rs221617495 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44182866 | GTATACTATTGGTAG[C/T]TAAAATGGAATATAT | 73469 |
rs221655123 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44144629 | ACCTGCGCAGAGTGG[A/G]AGAGCTCACCCTGGG | 73469 |
rs221656500 | in-del | -/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44227985 | AGACCCTGTCACACA[-/C]AAAAAAATAGCAAGA | 73469 |
rs221723619 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44229147 | GTTCTCCAGAATAAA[A/G]TAAATTCCAAAATAG | 73469 |
rs221760145 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44207640 | CCACTCTGACCTCTA[A/C]ACCATGGCAATCATA | 73469 |
rs221768144 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44179142 | AATCCCCTCCTACTG[A/G]AGTACACTAGGAACC | 73469 |
rs221828576 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44230398 | TATCTCTTCAGACTG[C/T]GCAAGGGTCTTTCTA | 73469 |
rs221829911 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44188638 | AACCTATTTGTTCCC[A/C]TTAGTCACCTGACAA | 73469 |
rs221885233 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44129873 | CTTCAAAACAAAAAT[A/G]CAAAAACAAAACAAA | 73469 |
rs221903196 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44202525 | TCATAGCAGCACTAT[A/G]AAGGCAGAAGCAAGA | 73469 |
rs221925557 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44190396 | AAGCTATATGTCTGA[C/T]TCTTTATATAGATGC | 73469 |
rs221927775 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44153827 | AAGCACAGAAAACAA[C/T]TGATTTTAGGAACAA | 73469 |
rs221952028 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44146555 | CCTCCCTCCACCACC[A/G]TCACCATCGTCTATA | 73469 |
rs221979091 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44171836 | TAGACCAGGCTGGCC[A/T]CGAACTCAGAAATCA | 73469 |
rs222024657 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44166263 | GCTCTAGTAAAGAAA[A/G]GAATTTATACATACG | 73469 |
rs222043653 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44211718 | AGGGAGGAAGGGAGA[A/G]AGGGGCCAAGATGGA | 73469 |
rs222082151 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44201647 | AGGCACAGGCATGGA[A/G]CGTGACCCACAGAGT | 73469 |
rs222084993 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44155175 | GACTGAACCAAAGAA[A/G]GAAGCTGAGCAACTC | 73469 |
rs222181492 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44174645 | GGCTCACAGCCATCC[G/T]TAATGAGATCTGACT | 73469 |
rs222236646 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44175334 | TACTATGGTTTATAT[A/G]AACTGTAGTAACCTA | 73469 |
rs222236785 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44165520 | AAACAACTAAAGACT[A/C]CTTGCTCCCTCTCCT | 73469 |
rs222273516 | in-del | -/TG | | | intron-variant | Rnf38 | Mm_Celera | 4:44174074 | TCTCTAAAAACTCAC[-/TG]TATGTTTTTGCTTTA | 73469 |
rs222283234 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44138448 | CCAGTGCTGGGATTA[C/T]AGGCCTGTGCTACCA | 73469 |
rs222308529 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44199471 | TTTACGTTACTAAAA[A/T]TTTTCTTTGATGAAT | 73469 |
rs222313095 | snp | C/T | | | upstream-variant-2KB | Rnf38 | Mm_Celera | 4:44234771 | TCAAAACACCATCAT[C/T]CCCCCTCCCCCCGGT | 73469 |
rs222329594 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44130801 | ATCACAGGTATGTAC[C/T]AGCACAGCAACTCTA | 73469 |
rs222339015 | snp | C/T | | | intron-variant, upstream-variant-2KB, synonymous-codon, utr-variant-5-prime | Rnf38 | Mm_Celera | 4:44167748 | GCCGTCCCCGATCGT[C/T]CTTGCCCTCGGAACC | 73469 |
rs222340607 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44177758 | AAACAAAAACAAAAA[A/C]AAAACCACAATCTAA | 73469 |
rs222368246 | in-del | -/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44172793 | GCCCTATCCAACCGG[-/C]CCGGCCTCTGGTCCT | 73469 |
rs222393442 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44142503 | TTTAAGTAAAAAATG[A/C]CAGAATATAAAATTT | 73469 |
rs222426883 | in-del | -/TT | | | intron-variant | Rnf38 | Mm_Celera | 4:44205845 | ATAATGGCACGAGGC[-/TT]TTTTTTTTTTTTTTA | 73469 |
rs222496830 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44134342 | TAGGCTGCCTTTTTA[A/T]ATAAAGATTAAGTAT | 73469 |
rs222501219 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44131953 | TAACCCCAGCACTAG[C/G]AGGTAGGGGAAGTCT | 73469 |
rs222527764 | in-del | -/GTTTTTGTTT | | | intron-variant | Rnf38 | Mm_Celera | 4:44164085 | TTTCTACTATATTCA[-/GTTTTTGTTT]TTTTTTTTTTCATAA | 73469 |
rs222555698 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44133231 | GTGAACTTTATGATA[C/T]GAATTTCAGCTCATT | 73469 |
rs222586958 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44141908 | CTCTGACTTCCATAT[A/G]CCATGCACCCCTCCC | 73469 |
rs222587085 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44162909 | CATCTAGGGAGGGAA[C/T]CTCAGTAGAGAAAAT | 73469 |
rs222631166 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44205265 | ATGCCAGACAAGTCA[C/T]GAGAAAAGAATGCGT | 73469 |
rs222635762 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44180116 | GGTATGATCACTTTT[A/G]CTTGATTGGCTTACA | 73469 |
rs222679338 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44137289 | CAAGACTCACACAAA[A/G]TTAAATCTAAAAAAA | 73469 |
rs222695904 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44141680 | CACCTGCACATATGG[C/T]GACACATGTGTATAC | 73469 |
rs222700359 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44170854 | TTTAAATTGGGACTT[C/T]GCTGAACCTGGAGAT | 73469 |
rs222710942 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rnf38 | Mm_Celera | 4:44169632 | GACAATCTAATGTGG[C/T]GGGGCAGAAATTATG | 73469 |
rs222717343 | in-del | -/AAAAAA | | | intron-variant | Rnf38 | Mm_Celera | 4:44198508 | GAAAAACCCAGTGTC[-/AAAAAA]AAAAAAAAAAAAAAA | 73469 |
rs222758860 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44178840 | GTTGTCATCTGACCT[C/T]CATCATGGTATGTGT | 73469 |
rs222767524 | snp | A/G | | | utr-variant-5-prime | Rnf38 | Mm_Celera | 4:44233565 | GGGCGCTCTGCCGCA[A/G]GCACCGACACCCTGC | 73469 |
rs222775200 | in-del | -/ATAC | | | intron-variant | Rnf38 | Mm_Celera | 4:44231729 | TTTAAACACATACAT[-/ATAC]ACATACATACATACA | 73469 |
rs222779847 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44198535 | AAAAACCAAACAAAC[-/A]AAAAAAAACCTCAAT | 73469 |
rs222871146 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44204723 | CCTCGAGTTCAATGA[C/T]AGCCTAGGTTACAGA | 73469 |
rs222945790 | in-del | -/AGGAGG | | | intron-variant | Rnf38 | Mm_Celera | 4:44224397 | GTGCTCCCGGCTTTC[-/AGGAGG]AGGAGGAGGAGGAGG | 73469 |
rs222955804 | in-del | -/AA | | | upstream-variant-2KB | Rnf38 | Mm_Celera | 4:44235558 | GATGAGTAGTTCACC[-/AA]AAGAAGGACAGCTCG | 73469 |
rs222975726 | snp | A/C | | | downstream-variant-500B | Rnf38 | Mm_Celera | 4:44125733 | GCTCTTTTCCAGGTA[A/C]TGGTTCATAATTAGG | 73469 |
rs223036596 | snp | C/G | | | upstream-variant-2KB, intron-variant | Rnf38 | Mm_Celera | 4:44168517 | CCAGCAACTCTAAAA[C/G]TCAGCAGTAGAGCAG | 73469 |
rs223068860 | in-del | -/CGTCACCATCGTCAT | | | intron-variant | Rnf38 | GRCm38.p3 | 4:44146553 | TCCTCCCTCCACCAC[-/CGTCACCATCGTCAT]CGTCACCATCGTCTA | 73469 |
rs223103413 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44212642 | TTCACCAGTTCTTCA[C/T]ACTGAGGAGGTAAAG | 73469 |
rs223210635 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44199529 | TATTTAGTATGCATA[G/T]GCATATGTGCAGGCA | 73469 |
rs223221718 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44144779 | CTTCATGACTGGGCA[A/G]TAACAGCATATCTAA | 73469 |
rs223243845 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44164668 | AAGCAAAATCACAAA[A/G]CCATTGAATCTAAAA | 73469 |
rs223274736 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44200367 | CTCCTATACCTGGAG[C/T]TACAGAGAGTTGAGA | 73469 |
rs223299986 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44177834 | GGTGGGAATATAAAG[A/G]ATATAGCCCTTTGGA | 73469 |
rs223311768 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44203659 | GCACATTTTGGAGGT[A/G]GAATGAAAATGGAAA | 73469 |
rs223354259 | in-del | -/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44225541 | ATCACCCTACACCTG[-/C]CCCTCATCACCTCAG | 73469 |
rs223372568 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44130040 | GGGGGGTTTGGAGGG[A/G]GGATAACAGGGCTGG | 73469 |
rs223421498 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44173325 | CCATTCGAGCTTCTT[-/A]AAAAAAAACCAGAAG | 73469 |
rs223430041 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44208476 | CTTTTGTTTCATTTT[A/G]TTCTTTGAGGTAGGG | 73469 |
rs223459214 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44145489 | GTTCCATTACCAGCA[A/C]CCAGCATAAAAATGT | 73469 |
rs223462273 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44207773 | TACAGATGATTCTGA[A/G]CTGCCACATGGTTGC | 73469 |
rs223478912 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44224074 | TAATTTCAGATTAGG[-/A]AAAAAAAAATGTCCC | 73469 |
rs223479410 | in-del | -/AAAACA | | | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44126791 | ATTCATGCAAAAACG[-/AAAACA]AAAACAAAAACAAAA | 73469 |
rs223519928 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44172054 | ACATTATAAATATAT[C/T]TTTAAGCACAGTATA | 73469 |
rs223531727 | in-del | -/AAAAAG | | | intron-variant | Rnf38 | Mm_Celera | 4:44137743 | TTTAAACTAAAAAAA[-/AAAAAG]AAAAAGAAAAACAAA | 73469 |
rs223548436 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44181079 | AGACATCTGGGTGCG[C/T]ATGCACACACACATA | 73469 |
rs223568898 | in-del | -/ACACACACAG | | | intron-variant | Rnf38 | Mm_Celera | 4:44214597 | CACACACACACACAC[-/ACACACACAG]AGACATATAAACACA | 73469 |
rs223584682 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44210441 | TGTGCTAGTACAGAG[C/T]TTGCTAGCATGCACA | 73469 |
rs223642356 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44202664 | ATTGAAAGTTCAAAG[C/T]CAACCTGGGCTATAA | 73469 |
rs223694207 | snp | A/G | | | upstream-variant-2KB | Rnf38 | Mm_Celera | 4:44234063 | TCTAGGGGGATCCTC[A/G]GCAGCCGCGGCCCGC | 73469 |
rs223699903 | snp | A/G | | | upstream-variant-2KB, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44221550 | AAAGCAAGAATCAAA[A/G]TCAAACTGTGAATTT | 73469 |
rs223700790 | in-del | -/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44188494 | ATTACTAGTTTCATA[-/T]TAATACAGATATTGG | 73469 |
rs223701435 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44177492 | TGACAGAAAAAGCAG[-/A]AAAACGTTCACCATC | 73469 |
rs223708045 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44134469 | TACTATGTAGTTCAA[A/G]CTTACTTTAAATGTG | 73469 |
rs223739318 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44161157 | CGTGCAAGTGGCTTG[C/T]GCCTCTGACCAGAGC | 73469 |
rs223798265 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44170713 | TGTGTACAAGACAGT[C/T]TCAAAAAGAAAAACG | 73469 |
rs223849784 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44203882 | acagacagacagaca[C/G]agaggcagagagaca | 73469 |
rs223850707 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44223376 | AAGTTTAAAGTCATT[C/T]TACATAGCAAGTTTG | 73469 |
rs223863999 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Rnf38 | Mm_Celera | 4:44168284 | GTAGCTCCGCCTCTT[-/C]CCCCCGCGCCGAGCC | 73469 |
rs223899339 | snp | C/T | | | upstream-variant-2KB, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44222055 | TTCTACCTTTTCTCT[C/T]TCCCCCCACTTTTCT | 73469 |
rs223899347 | snp | A/G | | | upstream-variant-2KB | Rnf38 | Mm_Celera | 4:44235372 | GATCTTAAGAGCCGG[A/G]CGTGGTGGCACACGC | 73469 |
rs223918111 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44160360 | GTCTGAAGACAGCTA[C/T]GGTGTACTTACATAT | 73469 |
rs223949553 | in-del | -/AAC | | | intron-variant | Rnf38 | Mm_Celera | 4:44152998 | TAAAAAAAAAAAAAA[-/AAC]ACCACCAAACAGCTA | 73469 |
rs224010502 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44226303 | GAATCTTTGATTAGG[A/G]TTAATGTAGTGTTAA | 73469 |
rs224022223 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44205350 | TGCACCCGTAGCTGT[C/T]CTGGAACTCAATGTG | 73469 |
rs224024751 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44196702 | AGAGTAACTCCAGCA[C/T]AGCAGTAGTGGCTGA | 73469 |
rs224054227 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44225589 | ATGGCACTCCTATCC[A/C]GTGAAGGAAACAAGA | 73469 |
rs224096062 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44197278 | AATGGAGGAGCTAGA[G/T]AAAGTATCCAAGGAG | 73469 |
rs224144768 | in-del | -/ACACAC | | | intron-variant | Rnf38 | Mm_Celera | 4:44182446 | TACCTACCTACCTAT[-/ACACAC]ACACACACACACACA | 73469 |
rs224151589 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44192219 | CACAAACTATTCAGA[C/G]ACTCTTGAAAAAGAT | 73469 |
rs224153558 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44232998 | CCAGCTCCCAAAATC[A/G]GCTCCCCAGGGCACT | 73469 |
rs224154291 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rnf38 | Mm_Celera | 4:44169680 | TAGTTTCAGCTAAAG[C/T]TTTGCTTGCTGTCTT | 73469 |
rs224179663 | snp | C/G | | | downstream-variant-500B, intron-variant | Mir5106, Rnf38 | Mm_Celera | 4:44220871 | TCCTCTAGAACTGAA[C/G]CCTGGTCCTCTGCAA | 73469 |
rs224194662 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44191387 | TGAAAAAGCTAGTAA[A/C]ACATGCAGGGCATGT | 73469 |
rs224211346 | in-del | -/TTT | | | intron-variant | Rnf38 | Mm_Celera | 4:44223520 | TTGCTTTTGTTTTTG[-/TTT]TTTTTTTTTCCTACT | 73469 |
rs224212253 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44232056 | TTTGTCAAGCCTTAC[G/T]TTCAAGACAATACCT | 73469 |
rs224219134 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44160487 | AAGTGAATGCTGTAG[C/T]ACTGCCATGCTTTGA | 73469 |
rs224261948 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44159505 | CATGTACAAATGTTA[A/C]GTTTAACTGAGGATG | 73469 |
rs224330378 | snp | G/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44203938 | AGGGAGAAAAAGAGA[G/T]GAAGAGAAAAGAAAG | 73469 |
rs224376361 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44196295 | CCAAAGGACAGGGAG[C/T]CCGCACCACTGCACT | 73469 |
rs224382737 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44195552 | ATTGTAAACAAAGTG[A/G]TTTAAAGCACTGACT | 73469 |
rs224432805 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44204522 | ACAAATAAATATAAA[A/G]AAGAAAAACAGAAGA | 73469 |
rs224444035 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44157820 | GACAGTGGTGGCGCA[A/C]GCCTTTTATCCCAGC | 73469 |
rs224444485 | in-del | -/TAGATAAA | | | intron-variant | Rnf38 | Mm_Celera | 4:44231689 | AAACACACAAATAAG[-/TAGATAAA]TAGATAAATAAATAA | 73469 |
rs224478581 | snp | A/G | | | intron-variant, utr-variant-5-prime | Rnf38 | Mm_Celera | 4:44167429 | AGGACCCCTCCAACC[A/G]GGTTCTGAGTTCTCC | 73469 |
rs224504273 | in-del | -/CACC | | | intron-variant | Rnf38 | Mm_Celera | 4:44159964 | ATAAAACGTGCTTAA[-/CACC]CACCGTGTGCTTTTA | 73469 |
rs224514490 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rnf38 | Mm_Celera | 4:44168436 | GCTCGGGCGGCGAAG[A/G]TGGGGAGGTGGGGCA | 73469 |
rs224523973 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44161610 | GGTCGGTTTTACAAA[A/T]CTCAAGTACAAGCAC | 73469 |
rs224525992 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44172174 | TTATACTAAAGGTTA[C/T]CACAATAATGGTTAT | 73469 |
rs224550135 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rnf38 | Mm_Celera | 4:44168948 | AAAGCTGAGAAAGAG[A/G]ACGAATAGGAGCTTT | 73469 |
rs224593563 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44141457 | AAAGGAGACTGTTTC[-/A]AAAAAACTTTACTAA | 73469 |
rs224644386 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44202764 | TTATAGGCACAGGTG[A/C]ACACACCTAACACTC | 73469 |
rs224711642 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44159163 | AGTTCTGTCAGCAGA[C/T]GGGGCAGGGCAAGAG | 73469 |
rs224750512 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44229009 | TCTAGCAAGTGAGCC[C/T]GTGACTCGGGTGGCT | 73469 |
rs224787585 | snp | C/T | | | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44126967 | AGGCCACCACATCCT[C/T]TGTCGCCTGGTGCGC | 73469 |
rs224823388 | in-del | -/ATATATATATA | | | intron-variant | Rnf38 | Mm_Celera | 4:44230469 | ATTATATATATATAT[-/ATATATATATA]TATTTTATTTTATAT | 73469 |
rs224837434 | in-del | -/ACA | | | intron-variant | Rnf38 | Mm_Celera | 4:44145607 | ACTTGTACTAGGTAC[-/ACA]ACAACAACTGTCACT | 73469 |
rs224838769 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44157547 | gtatatatatatata[C/T]atatatatatatata | 73469 |
rs224852701 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44166759 | CATATATACTAGTAT[C/G]TTTCTAAAGTAAAAG | 73469 |
rs224933926 | in-del | -/AAAAA | | | intron-variant | Rnf38 | Mm_Celera | 4:44223351 | TTTTAAAAATACATT[-/AAAAA]AAAAAAAAGAAGTTT | 73469 |
rs224941752 | snp | A/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44227847 | CCAACTGGATTAAGA[A/T]GGGCATGGCCAATCA | 73469 |
rs224952611 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44201483 | ATCTAGATCCATTTC[A/G]TGGGAAAGATCTTTG | 73469 |
rs224982560 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44189948 | AGCCATGCAAAGTAC[C/T]ACACACCCGTAACCC | 73469 |
rs224999646 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44132965 | AAGGAAGAAAGGAAG[A/G]AAGAAAGGAAGGAAG | 73469 |
rs225000772 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44181370 | ACATGACCAGCACAC[A/G]TCCTTAAGAAGCTGC | 73469 |
rs225001866 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44225892 | GAAAGCACTCTGCCA[C/T]CATTTGCAAAGGCAG | 73469 |
rs225012890 | in-del | -/A | | | intron-variant | Rnf38 | Mm_Celera | 4:44194345 | AAAACAAAACAAAAC[-/A]AAAAGAAACAAAAAA | 73469 |
rs225030468 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44165295 | AGCAGTGGGCAAGAG[A/C]GCCTGTCTCAAGACA | 73469 |
rs225037966 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44190535 | GCGGTGATGGCACAC[A/G]CCTTTAATCCCAGTA | 73469 |
rs225053556 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44180674 | CAAACATGTTTTGGC[C/T]CATGGTCCTATATTA | 73469 |
rs225066489 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44174595 | CTGACTGCTCTTCCG[A/G]AGGTCCTGAGTTCAA | 73469 |
rs225066684 | in-del | -/AGAAATAACATAA | | | intron-variant | Rnf38 | Mm_Celera | 4:44214831 | CCCTACTCTAAAAAC[-/AGAAATAACATAA]ATAAATAAATAAATA | 73469 |
rs225093122 | in-del | -/AC | | | intron-variant | Rnf38 | Mm_Celera | 4:44130538 | AGGGAGGTTTGTAAA[-/AC]ACAGCTGCGGTAGGT | 73469 |
rs225103862 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44200605 | CTAAACTCATACAAA[C/G]TTTAAATAAATGAAG | 73469 |
rs225129286 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44149658 | TATCTGTGCAGATCC[A/G]AGGCCAACGTGCAGA | 73469 |
rs225139386 | snp | A/C | | | intron-variant | Rnf38 | Mm_Celera | 4:44232156 | GTCTATAACATATTA[A/C]AACTGTCCTTACCAA | 73469 |
rs225167677 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44148153 | AAAAATGATTTGCAG[A/G]GGGTAGAGAGATGGT | 73469 |
rs225167701 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44161271 | GAGATAAGACGTATA[C/T]TTGCCATTCTTGATC | 73469 |
rs225171737 | snp | A/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44231218 | CACATATACATATAG[A/G]TGGAAATACATGCTA | 73469 |
rs225191911 | in-del | -/AG | | | utr-variant-3-prime | Rnf38 | Mm_Celera | 4:44127062 | GGCCATGGAGACCGT[-/AG]GCAAGTGTGCACCTA | 73469 |
rs225236014 | snp | C/G | | | intron-variant | Rnf38 | Mm_Celera | 4:44214606 | ACACACACACACACA[C/G]AGACATATAAACACA | 73469 |
rs225279670 | in-del | -/CT | | | intron-variant | Rnf38 | Mm_Celera | 4:44160881 | AGGGCTTGCCACCAA[-/CT]CTGATGGCCTGGATT | 73469 |
rs225299815 | snp | C/T | | | intron-variant | Rnf38 | Mm_Celera | 4:44195658 | CCCTCTTCTGGTGTG[C/T]CTGAAAGTAGCATAT | 73469 |