SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6152772 | snp | A/T | 0.49827 | 0.0293608 | intron-variant | Dcaf17 | Mm_Celera | 2:71096634 | TGTCTTCTTGACTAA[A/T]AATGTTTTTATTAAA | 75763 |
rs6168080 | snp | A/G | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71097143 | tgttgaaggacattg[A/G]ggttctttatattcc | 75763 |
rs6168147 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71097180 | GTCTTGAATAGAGCA[A/G]CAGTATGGCTGAATG | 75763 |
rs6169828 | snp | C/G | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71097452 | ctgcctctacctccc[C/G]aatgctgggattatg | 75763 |
rs6169924 | snp | C/T | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71097503 | atttctgcttattct[C/T]ttgagaagtctgttc | 75763 |
rs6184186 | snp | A/G | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71097795 | cacacctccacaccc[A/G]tgtcatgttgggtac | 75763 |
rs6400729 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054779 | TTCCATTTAAAACAA[C/T]AAAATGAAACGGNTA | 75763 |
rs6400763 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054792 | AANAAAATGAAACGG[C/T]TAACGTTTGATCCAG | 75763 |
rs6401211 | snp | A/C | 0.456747 | 0.140554 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054854 | CAGAAAGCTGGTGTG[A/C]TTACTGACTTTTTCT | 75763 |
rs6401865 | snp | G/T | 0.49827 | 0.0293608 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71055021 | AGTAATTTTGAACAC[G/T]CAGGCTGAGCTAGTT | 75763 |
rs6402365 | snp | C/T | 0.456747 | 0.140554 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71055092 | ATTATCTTAGGCAGT[C/T]CAATAAGAATGCAAA | 75763 |
rs6402844 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71055136 | ATTCCCTATAAGGGG[A/G]AAAAATGGAAGGAGG | 75763 |
rs6403489 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71055270 | CAGCAACTTTCACCA[A/C]TAATTACCATACAAA | 75763 |
rs6412540 | snp | C/T | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71096377 | catgaccaccggagc[C/T]ngaccaagtggcact | 75763 |
rs6412542 | snp | G/T | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71096378 | atgaccaccggagcn[G/T]gaccaagtggcacta | 75763 |
rs13472434 | snp | C/T | 0.456747 | 0.140554 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71055911 | CCGCGTCAGCCTTCC[C/T]TTGAGGTTCGCAGGT | 75763 |
rs13472435 | snp | A/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090479 | AACAAAACATAAAGA[A/T]ATACTATATACTCTA | 75763 |
rs27971666 | snp | C/G | 0.401235 | 0.199068 | downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71114613 | CACAATAAGGCAAAA[C/G]GTGAGCCATCCATTA | 75763 |
rs27971667 | snp | C/T | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71114273 | GAAAGTGTAGTCTAC[C/T]CATTAGCAGGGTTCT | 75763 |
rs27971668 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Dcaf17 | Mm_Celera | 2:71113920 | ATAGCCCGGTTCCTT[A/G]CACTGTTTAATGTCC | 75763 |
rs27971669 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Dcaf17 | Mm_Celera | 2:71113753 | AAACGATTTCTGAGG[A/T]CTTGTTGCCTATGAA | 75763 |
rs27971670 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Dcaf17 | Mm_Celera | 2:71113690 | CATGCTTACACAATC[C/T]TTTCACACTTCAATA | 75763 |
rs27971671 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dcaf17 | Mm_Celera | 2:71113292 | AGAGATATGGTTTAG[C/T]CTTCCCATGATCCAG | 75763 |
rs27971672 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Dcaf17 | Mm_Celera | 2:71112227 | GTGGCTCGTCCCAAA[C/T]TTCTTCCTGTTGTCT | 75763 |
rs27971673 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71112162 | ACTTCTCCTGCTCCT[A/G]GTTAACAAATTACAG | 75763 |
rs27971674 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Dcaf17 | Mm_Celera | 2:71111402 | ATCAGAATGGTAACC[A/G]GACTTTGTAAGACAG | 75763 |
rs27971675 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Dcaf17 | Mm_Celera | 2:71111387 | ATATACTCCTGTCAC[A/G]TCAGAATGGTAACCG | 75763 |
rs27971676 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Dcaf17 | Mm_Celera | 2:71111205 | TGCATGCCAATCACC[A/G]TCCATAAACAAAAAC | 75763 |
rs27971677 | snp | A/G | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71111187 | CAGGCCCTGAGTGCC[A/G]ACTGCATGCCAATCA | 75763 |
rs27971678 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Dcaf17 | Mm_Celera | 2:71111093 | CCTCATCTGGGGCTT[C/T]GGCAAGGAGGTATTA | 75763 |
rs27971679 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Dcaf17 | Mm_Celera | 2:71111036 | GCATGAGAGCCATGC[A/G]TCGTGCTGTATTAGT | 75763 |
rs27971680 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Dcaf17 | Mm_Celera | 2:71110942 | AGCATTAAACCGACG[C/G]AAACATGCATCTGAT | 75763 |
rs27971681 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Dcaf17 | Mm_Celera | 2:71110382 | TGTTTCTGATAAGGA[C/T]ATAACAAGGCCGATT | 75763 |
rs27971682 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71110290 | GGAAGCTCACAGGAC[A/C]GTGGGCCTTAGACAT | 75763 |
rs27971683 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Dcaf17 | Mm_Celera | 2:71110226 | TCCCTCAGGCAGTAA[G/T]GGCTGCTCTGTATCT | 75763 |
rs27971684 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Dcaf17 | Mm_Celera | 2:71110224 | GTTCCCTCAGGCAGT[A/G]AGGGCTGCTCTGTAT | 75763 |
rs27971685 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dcaf17 | Mm_Celera | 2:71110008 | TAAACTGGTCCTCCT[C/T]TCCTacacacacaca | 75763 |
rs27971686 | snp | C/T | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71109967 | AGACTCTGACATGAG[C/T]CTATGTAAATGCTGC | 75763 |
rs27971687 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71108745 | GATCTCGTTCCTTTC[A/T]TGACCTGAGACAGAT | 75763 |
rs27971688 | snp | A/G | 0.49827 | 0.0293608 | intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71107585 | GAACCCAGTCGAGTC[A/G]CCCATTGCTGACATC | 75763 |
rs27971689 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dcaf17 | Mm_Celera | 2:71107423 | TGCTTCTAGTACCTT[C/T]TAACCAATAACAGCT | 75763 |
rs27971690 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Dcaf17 | Mm_Celera | 2:71107218 | CTCCAGCAGTCATCC[A/G]GGAATTTTAAAAAGC | 75763 |
rs27971691 | snp | A/G | 0.489796 | 0.070696 | intron-variant, utr-variant-3-prime, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71106219 | CAGGACATGCCAAGC[A/G]AGCCCAGTGCTACTG | 75763 |
rs27971692 | snp | A/G | 0.48 | 0.0979796 | intron-variant, utr-variant-3-prime, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71106190 | TTTTTCAGTTGGAGT[A/G]CTGGGATCCAACCCA | 75763 |
rs27971693 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Dcaf17 | Mm_Celera | 2:71105636 | CTCACCAGCTGTTCA[A/G]TCTTTCCTGTTTGTG | 75763 |
rs27971694 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Dcaf17 | Mm_Celera | 2:71105517 | TCACAGAATTGCCAA[A/T]GTCGGGAAGGCAAAT | 75763 |
rs27971695 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Dcaf17 | Mm_Celera | 2:71104997 | CCTGGGAGAGAAGAG[G/T]CCAAGGCTGTGATCT | 75763 |
rs27971696 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71104936 | AGGCCCACAGCAAAT[C/T]GGAGAAACCCATGCT | 75763 |
rs27971697 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Dcaf17 | Mm_Celera | 2:71104756 | TTAGCTTAGAACATC[A/G]TGTAGTTAAAGATTC | 75763 |
rs27971698 | snp | A/G | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71104615 | GGTTACTCTAATTTT[A/G]CATATAGCTGGCCCT | 75763 |
rs27971699 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71104284 | CTGGCACCTAGCCCA[A/G]CATCCTTTGGAGATT | 75763 |
rs27971700 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Dcaf17 | Mm_Celera | 2:71104254 | CCTTTACATATATCA[C/T]AACTGACTTGAAGTC | 75763 |
rs27971701 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Dcaf17 | Mm_Celera | 2:71104169 | TAGTACAGTAGATGC[A/C]TTACAGGGATCTCTT | 75763 |
rs27971702 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Dcaf17 | Mm_Celera | 2:71104140 | AAGGTGGTCAGTTCC[C/G]TGTTGGGGTCCTATA | 75763 |
rs27971703 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Dcaf17 | Mm_Celera | 2:71104034 | AGATGGGATATGTAG[C/T]CCTTAGAACTTTAAA | 75763 |
rs27971704 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Dcaf17 | Mm_Celera | 2:71103926 | GTGTTTGAATTGGCA[C/T]TAAATGAAGAGAAGC | 75763 |
rs27971705 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Dcaf17 | Mm_Celera | 2:71103889 | TCAGCATTCCAGCAG[A/G]AGGGAGAAGTCATGT | 75763 |
rs27971706 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Dcaf17 | Mm_Celera | 2:71103661 | TCCAATCTAGGGTTT[C/T]TGAGTCCTCTGTCTT | 75763 |
rs27971707 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Dcaf17 | Mm_Celera | 2:71103609 | ATAAAGGCTAAAACA[A/G]TTACTCTCTTGTCTT | 75763 |
rs27971708 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Dcaf17 | Mm_Celera | 2:71103541 | CGACAGCTGCATTTG[C/T]GCCACACTGAGAGCT | 75763 |
rs27971709 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Dcaf17 | Mm_Celera | 2:71103521 | TGTACCTCTGATTGT[A/G]CTGTCGACAGCTGCA | 75763 |
rs27971710 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Dcaf17 | Mm_Celera | 2:71103499 | GCCTGTTTGAGGAAG[C/T]GAAATTTGTACCTCT | 75763 |
rs27971711 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Dcaf17 | Mm_Celera | 2:71103437 | AGGGAGGCCAAGATC[A/T]TACAGCGAAGGCTGT | 75763 |
rs27971712 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71103409 | ATGAAGGCTCTGAGG[C/T]ATAGGCTCATACAGG | 75763 |
rs27971713 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Dcaf17 | Mm_Celera | 2:71103370 | TTGTTAAAGAATTGA[A/G]ACCCAGTTTAAGTCT | 75763 |
rs27971714 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71103333 | ATAGTAACCAATGGG[A/C]TGAAATTGTAGAACC | 75763 |
rs27971715 | snp | A/T | 0.495868 | 0.0452663 | intron-variant | Dcaf17 | Mm_Celera | 2:71103311 | TATTCTGCCTAGAAG[A/T]GTGGAGATAGTAACC | 75763 |
rs27971716 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Dcaf17 | Mm_Celera | 2:71103254 | AGTGAGAAGGTTTGC[A/C]GTGTTTCAGAAATCA | 75763 |
rs27971717 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Dcaf17 | Mm_Celera | 2:71103240 | CTGAGATGCTCTGAA[A/G]TGAGAAGGTTTGCAG | 75763 |
rs27971718 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dcaf17 | Mm_Celera | 2:71103006 | AGAAACAGTCTCCAT[C/T]TTCCTCCCAGGTGGT | 75763 |
rs27971719 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Dcaf17 | Mm_Celera | 2:71102983 | AACCATGCTGTGGGC[A/G]TTCCTACAGAAACAG | 75763 |
rs27971720 | snp | A/G | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71102974 | TACTTAGTAAACCAT[A/G]CTGTGGGCATTCCTA | 75763 |
rs27971721 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71101648 | AACGGGCAGAGTGGT[A/G]TTAGTCCAGGACCCA | 75763 |
rs27971722 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Dcaf17 | Mm_Celera | 2:71101424 | CATCACATGGAAATC[A/G]GCTTCAAGGCAGAAG | 75763 |
rs27971723 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Dcaf17 | Mm_Celera | 2:71101382 | AAAAGGAGAGATGGT[C/T]CTACTGTATCAGTGA | 75763 |
rs27971724 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Dcaf17 | Mm_Celera | 2:71101291 | TCTTGGATGAGGCCT[A/G]AGAAAATCTGTTTGG | 75763 |
rs27971725 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Dcaf17 | Mm_Celera | 2:71101211 | GTGCGCAAGACCTGA[A/G]CTTCATCCCAGTAGT | 75763 |
rs27971726 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71101200 | AGATGCATACTGTGC[A/G]CAAGACCTGAGCTTC | 75763 |
rs27971727 | snp | G/T | 0.486111 | 0.0821678 | intron-variant | Dcaf17 | Mm_Celera | 2:71101165 | CAGGATGTGGACCCA[G/T]GGATGAGACTCTGTT | 75763 |
rs27971728 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Dcaf17 | Mm_Celera | 2:71100871 | GTTTTCATCACACAT[A/T]GCTTGGTTGAAGGCT | 75763 |
rs27971729 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Dcaf17 | Mm_Celera | 2:71100840 | TGGACACTATGTAGC[A/T]GGGAGAAAGCTTAGT | 75763 |
rs27971730 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71100748 | TGCTCCTGCAGTAGT[A/G]TAGGCACCCATGGAT | 75763 |
rs27971731 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Dcaf17 | Mm_Celera | 2:71100692 | CACCATGGACACGCA[C/T]CATGGGACCCTACAT | 75763 |
rs27971732 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Dcaf17 | Mm_Celera | 2:71100633 | GGAAGCTCAAAACCA[A/T]TTAAGACTGGTGGTT | 75763 |
rs27971733 | snp | C/T | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71100630 | TGAGGAAGCTCAAAA[C/T]CAATTAAGACTGGTG | 75763 |
rs27971734 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Dcaf17 | Mm_Celera | 2:71100600 | ATGGAGACATGGCTG[A/C]TACTGCCTGCTGAAT | 75763 |
rs27971735 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71100559 | AAGGCTGAGCCAACT[C/G]GCTGACTGGAAGAAG | 75763 |
rs27971736 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Dcaf17 | Mm_Celera | 2:71100293 | TTCAGTCCCACATAT[C/T]CATTCATTATGTATC | 75763 |
rs27971737 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Dcaf17 | Mm_Celera | 2:71100123 | CTGCATGTACAAAAC[A/G]TGTGAGACATATGCT | 75763 |
rs27971738 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Dcaf17 | Mm_Celera | 2:71099977 | GCCTGAGCTACATGG[C/T]GACACCTCATCTAGA | 75763 |
rs27971739 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71099936 | GCATGTTGCAATCCT[A/G]ACACTGAGTCATGAG | 75763 |
rs27971740 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71099931 | GTGAGGCATGTTGCA[A/G]TCCTAACACTGAGTC | 75763 |
rs27971741 | snp | C/T | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71099759 | AGGATATCCACAGTC[C/T]ATAAGTTAGTGACTC | 75763 |
rs27971742 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Dcaf17 | Mm_Celera | 2:71099729 | CTTCCTCTGCAGGGA[C/T]CAGGTGACCTAGCCA | 75763 |
rs27971743 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Dcaf17 | Mm_Celera | 2:71098679 | CTTTGCCATGTATCC[A/G]GGTTCCTCTGTTGGA | 75763 |
rs27971744 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Dcaf17 | Mm_Celera | 2:71098600 | GTTATAGAAACATTT[C/T]CTCCTAAGTTAGATT | 75763 |
rs27971745 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Dcaf17 | Mm_Celera | 2:71098473 | AAAAGTTTACAAAAG[C/T]TCACATTGTTCTCAA | 75763 |
rs27971746 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Dcaf17 | Mm_Celera | 2:71098392 | AGTAAGTTAACCTAT[C/T]ATTAGATTGTAACAT | 75763 |
rs27971747 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Dcaf17 | Mm_Celera | 2:71098347 | CTTATCACATTAAAA[G/T]TCCAATGTTAAAAAT | 75763 |
rs27971748 | snp | A/G | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71098264 | TCTAAGTGCTCCACA[A/G]TAGCAATATTCGCAG | 75763 |
rs27971749 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Dcaf17 | Mm_Celera | 2:71096677 | TTTGATTTATTTTTA[C/T]AGAATTGTGGATAAG | 75763 |
rs27971750 | snp | A/G | 0.132653 | 0.220748 | downstream-variant-500B, intron-variant | Dcaf17 | Mm_Celera | 2:71096274 | ATTGTTCCTTATCAG[A/G]CACAGAACACTTTGG | 75763 |
rs27971751 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B, intron-variant | Dcaf17 | Mm_Celera | 2:71096140 | GATGTTTCTCCATGT[A/G]TCCATCAGCCCTCTT | 75763 |
rs27971752 | snp | A/C | 0.487535 | 0.077957 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71095638 | ATTGGGTCATGCATT[A/C]CCAGCGTATGCAGGC | 75763 |
rs27971753 | snp | G/T | 0.498615 | 0.0262793 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71095473 | TCTTTTATTACCAAT[G/T]TTCAGTGCATTTCAA | 75763 |
rs27971754 | snp | C/T | 0.487535 | 0.077957 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71095315 | CTGTGGGTGTGATCT[C/T]TGTCTCACATGGAAA | 75763 |
rs27971755 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71094896 | AGCACCTAGAAAGTT[A/G]TGTGTGTGATAATTG | 75763 |
rs27971756 | snp | A/G | 0.493827 | 0.0552116 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71094803 | CTTTGTTTGTTTTGC[A/G]TGGTCTGTATTCCGC | 75763 |
rs27971757 | snp | G/T | 0.459184 | 0.136902 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71094797 | GGTGGTCTTTGTTTG[G/T]TTTGCATGGTCTGTA | 75763 |
rs27971758 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71094670 | CCTGTTGAAAATAAC[A/C]ACTTGAGGTATAAAT | 75763 |
rs27971759 | snp | C/T | 0.475309 | 0.108333 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71094617 | TGTGAGTCTGAATGG[C/T]TTGTGTCTGCTGCTG | 75763 |
rs27971760 | snp | C/T | 0.493827 | 0.0552116 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71094574 | ATCTTCTGTGCCGTC[C/T]AGGCTATGATGAGCC | 75763 |
rs27971761 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71094431 | ATTTGAGCAGCTTAG[C/T]AACCCTTCCTTATGT | 75763 |
rs27971762 | snp | A/C | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71093946 | AATAATAGCAGTAGC[A/C]ACAACAAAGCCAACG | 75763 |
rs27971763 | snp | C/T | 0.493827 | 0.0552116 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71093936 | CCAGTGCTGGAATAA[C/T]AGCAGTAGCAACAAC | 75763 |
rs27971764 | snp | C/T | 0.497778 | 0.0332592 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71093681 | AACACACACACAGAG[C/T]AAAAGAGAGAGCCAG | 75763 |
rs27971765 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71093364 | GAGACATTTCTTAGA[C/T]ACGTGGTAAGAAAAA | 75763 |
rs27971766 | snp | G/T | 0.48 | 0.0979796 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71092902 | TTTGTTGTTTGAGTG[G/T]TTTTTGTTTGGATAG | 75763 |
rs27971767 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71092722 | AAGTCTAATACTCAC[A/G]TCTAGAGACTGAAGA | 75763 |
rs27971768 | snp | A/G | 0.498615 | 0.0262793 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71092436 | AAGGTGCTTTTATGC[A/G]GTATCTTAACTGTAC | 75763 |
rs27971769 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71092411 | ATTTGTGTCTTGTAT[A/G]CATAACCTGAAGGTG | 75763 |
rs27971770 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091894 | TTTTGTCCTGACCCC[A/G]TGTTAAGAATGGTGT | 75763 |
rs27971771 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091516 | CCCGGTCATCTCATT[C/T]TTCCAAGTCGTCCTC | 75763 |
rs27971772 | snp | C/T | 0.459184 | 0.136902 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091487 | TTCTGAGAAACCCAG[C/T]TGCTCAGAATCTCCC | 75763 |
rs27971773 | snp | C/G | 0.497778 | 0.0332592 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091433 | AATGTTAGTTAAAAG[C/G]AACCTGCGTGTAGGG | 75763 |
rs27971774 | snp | C/G | 0.132653 | 0.220748 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091373 | TTTTCTTCTGTGTTA[C/G]AACAGATTTAAACAT | 75763 |
rs27971775 | snp | A/C | 0.497778 | 0.0332592 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091303 | GGAGTTCTTTCCTGC[A/C]TGGGAGTAACCTCAT | 75763 |
rs27971776 | snp | C/T | 0.48 | 0.0979796 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090651 | TCATCAGTTCTTATG[C/T]GGTCTTATTGACTGT | 75763 |
rs27971777 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090563 | TTTGAGCCAAAAATT[A/G]CCACAGCTTCTTTGT | 75763 |
rs27971778 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090245 | TTGATGCAGGGATAA[C/T]TAATTCTTAAAGACT | 75763 |
rs27971779 | snp | C/G | 0.48 | 0.0979796 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090159 | ATTTTGAAACATTTC[C/G]ATTAGGTGCTAACGT | 75763 |
rs27971780 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090132 | CTAGGATGCTGTCCC[A/G]AGAGACCAAGCATTT | 75763 |
rs27971781 | snp | C/T | 0.497041 | 0.0383476 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090116 | CTTATGTAAAAGCTC[C/T]CTAGGATGCTGTCCC | 75763 |
rs27971782 | snp | C/T | 0.486111 | 0.0821678 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090107 | GGACTCCATCTTATG[C/T]AAAAGCTCCCTAGGA | 75763 |
rs27971783 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71089732 | GCTATGGGATTTTGG[C/T]GACACTGTGAATATA | 75763 |
rs27971784 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Dcaf17 | Mm_Celera | 2:71089724 | GGGTAGGTGCTATGG[G/T]ATTTTGGTGACACTG | 75763 |
rs27971785 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Dcaf17 | Mm_Celera | 2:71089687 | CAAGTCTTCTGCATC[A/G]GTGTGCATATGTAGG | 75763 |
rs27971786 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Dcaf17 | Mm_Celera | 2:71089602 | CCAGAGCTCTTTCTA[G/T]TCTCTACATTTTCTG | 75763 |
rs27971787 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71089560 | AGTGCTGTTCTGACA[C/T]TGAACTGCATAGCTA | 75763 |
rs27971788 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Dcaf17 | Mm_Celera | 2:71089534 | TTGTACGTGCTCCTG[C/G]GTCAGACAGAAGTGC | 75763 |
rs27971789 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Dcaf17 | GRCm38.p3 | 2:71089417 | TCCACACACATGTGA[A/C/G]CATACTCACGTTCCA | 75763 |
rs27971790 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71089155 | AAGAAGTTTCAAGAG[G/T]ACTGGGGAGATGGTT | 75763 |
rs27971791 | snp | C/T | 0.48 | 0.0979796 | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71089034 | CAAGCAATGATTAAG[C/T]AAGTTGGGTTCTAGC | 75763 |
rs27971792 | snp | G/T | 0.497778 | 0.0332592 | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71088924 | GTGATTCTTAAGACA[G/T]GTTATTTCCTTACCA | 75763 |
rs27971793 | snp | C/T | 0.48 | 0.0979796 | intron-variant, missense | Dcaf17 | Mm_Celera | 2:71088513 | ATGTGGTATGTATAA[C/T]GTCTGGGACACTAAG | 75763 |
rs27971794 | snp | A/G | 0.497778 | 0.0332592 | synonymous-codon, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71088490 | CATCCCACTAGTGGA[A/G]TCATGGGATGTGGTA | 75763 |
rs27971795 | snp | A/G | 0.48 | 0.0979796 | synonymous-codon, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71088454 | TTTCCACTGTAATGA[A/G]TATGGAACCTTACTC | 75763 |
rs27971796 | snp | A/G | 0.48 | 0.0979796 | synonymous-codon, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71088385 | AGATGAGTTGGACTT[A/G]CTTTCCGTAGTAGCT | 75763 |
rs27971797 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71088342 | ACTTTCATCTGTTCC[A/C]CAAGACTTTCAAAAT | 75763 |
rs27971798 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Dcaf17 | Mm_Celera | 2:71088150 | TTTGCCAAGTCCATG[A/G]GCTACTGCTTAACAT | 75763 |
rs27971799 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71088145 | AGTTGTTTGCCAAGT[C/T]CATGGGCTACTGCTT | 75763 |
rs27971800 | snp | G/T | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71087622 | TATTGTTTTTGTAAG[G/T]TATGCATTTTGTTTG | 75763 |
rs27971801 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Dcaf17 | Mm_Celera | 2:71087412 | AGGTATTCCTTAGCC[A/C]AAGATAACCAACAGT | 75763 |
rs27971802 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71087234 | CAGCTGGTTTGCCCG[C/T]ACTTGGGGACTGTTG | 75763 |
rs27971803 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71087022 | CTTTTAGTTTTCTGT[C/T]CTGTGTTAAGGCAAA | 75763 |
rs27971804 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Dcaf17 | Mm_Celera | 2:71086973 | GTGTATAAGCTGAGG[A/C]CCTTAAAGAGGGAGG | 75763 |
rs27971805 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71086759 | ACATGAGGAACTAGT[C/T]GTACTCCCACTTACA | 75763 |
rs27971806 | snp | G/T | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71086723 | AACATCATAACTCTT[G/T]GGAATCTGTTCTCTT | 75763 |
rs27971807 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Dcaf17 | Mm_Celera | 2:71086693 | TGTAATATGGATGTT[C/T]GCCTCATAGCTGCAA | 75763 |
rs27971808 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Dcaf17 | Mm_Celera | 2:71086328 | ACCTGTGTAAGCACC[A/T]CGACTCATAGCTGCA | 75763 |
rs27971809 | snp | C/T | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71086275 | GAGATGAGCTTTGCA[C/T]TGTAGTGTCATTCAC | 75763 |
rs27971810 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71086268 | AGAGGGAGAGATGAG[C/T]TTTGCACTGTAGTGT | 75763 |
rs27971811 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71086201 | TGTGTGTTCTACAGA[A/C]ACAACAGTGCAACTC | 75763 |
rs27971812 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Dcaf17 | Mm_Celera | 2:71086186 | AGTACTATGCTTAGC[C/T]GTGTGTTCTACAGAC | 75763 |
rs27971813 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Dcaf17 | Mm_Celera | 2:71086145 | TCCAATTAATTGCTG[C/T]CCTGTCTCTCTCATT | 75763 |
rs27971814 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Dcaf17 | Mm_Celera | 2:71086133 | AAAGTCTAGCATTCC[A/G]ATTAATTGCTGCCCT | 75763 |
rs27971815 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71086043 | ATGAGATCATTTATA[A/C]TCTGCAAATCCGAAT | 75763 |
rs27971816 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Dcaf17 | Mm_Celera | 2:71085925 | CCTATGGGACTTGGA[G/T]CTTTGAGAACATTGT | 75763 |
rs27971817 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Dcaf17 | Mm_Celera | 2:71085239 | GCTGTTGGCTGTTGA[C/T]CTTCTGCTTAAAATG | 75763 |
rs27971818 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71085238 | TGCTGTTGGCTGTTG[A/T]CCTTCTGCTTAAAAT | 75763 |
rs27971819 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Dcaf17 | Mm_Celera | 2:71085171 | CAGTCTCCGGGCCCT[C/T]CAGGCAGGATGATGA | 75763 |
rs27971820 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Dcaf17 | Mm_Celera | 2:71084588 | GCAATTTTTGTAATG[C/T]TTATTGACATTGTTG | 75763 |
rs27971821 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Dcaf17 | Mm_Celera | 2:71084330 | ACTTTAGCTGCTTCA[A/G]TTTTCTTCCCTGTAC | 75763 |
rs27971822 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71084300 | TCAGGTTGATTTGGC[C/G]CTCACACCTGTCCCA | 75763 |
rs27971823 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71084278 | GACTGTAAGTGTTCA[A/G]AATGTCTCAGGTTGA | 75763 |
rs27971824 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Dcaf17 | Mm_Celera | 2:71084240 | GGTCTACGCATGGCA[C/T]GGAGCAAATCCATGC | 75763 |
rs27971825 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71084228 | ACAGGAGCCTCAGGT[C/G]TACGCATGGCACGGA | 75763 |
rs27971826 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Dcaf17 | Mm_Celera | 2:71084205 | AACACAAAGTGCATG[C/T]GTGAGATACAGGAGC | 75763 |
rs27971827 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71084056 | CTATTTAATAGGTTC[C/T]AAACATTGGGCTAAT | 75763 |
rs27971828 | snp | C/T | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71084018 | TAGTATTGGAAAGTT[C/T]GTGGACTTTGGAGTC | 75763 |
rs27971829 | snp | A/G | 0.152778 | 0.230321 | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71083920 | TTTGGTTACGTGCTT[A/G]TGTGAGTGTTCCCTA | 75763 |
rs27971830 | snp | G/T | 0.244898 | 0.249948 | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71083772 | TTCCTTTATTTTGAT[G/T]TCTAAGCATACCTAC | 75763 |
rs27971831 | snp | C/G | 0.489796 | 0.070696 | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71083769 | TTTTTCCTTTATTTT[C/G]ATGTCTAAGCATACC | 75763 |
rs27971832 | snp | A/G | 0.498615 | 0.0262793 | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71083547 | GCCAAAGCTGGTATT[A/G]GTTCCTGGTGCTGCT | 75763 |
rs27971833 | snp | A/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71083545 | TTGCCAAAGCTGGTA[A/T]TAGTTCCTGGTGCTG | 75763 |
rs27971834 | snp | A/G | 0.465374 | 0.126941 | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71083336 | TTTCTGCAGTCACCA[A/G]TGCCTCTTTCTCTCC | 75763 |
rs27971835 | snp | C/G | 0.456747 | 0.140554 | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71083039 | TTGCACAGTCAGCCA[C/G]TGTGGGCTCCATTTA | 75763 |
rs27971836 | snp | A/T | 0.493827 | 0.0552116 | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71082828 | CTACCATGGTCAGGC[A/T]TACATTTTCTTCCTT | 75763 |
rs27971837 | snp | C/T | 0.492188 | 0.0620098 | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71082812 | AATCATTTGTTGAGG[C/T]CTACCATGGTCAGGC | 75763 |
rs27971838 | snp | C/T | 0.487535 | 0.077957 | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71082633 | CAGAACCAGATGGAG[C/T]TCACAGTGTTGGCGC | 75763 |
rs27971839 | snp | A/T | 0.152778 | 0.230321 | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71082563 | AACTGTTGCTAGAGT[A/T]GGCTTAGGCTGCCTC | 75763 |
rs27971840 | snp | C/G | 0.473373 | 0.11227 | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71082561 | GGAACTGTTGCTAGA[C/G]TAGGCTTAGGCTGCC | 75763 |
rs27971841 | snp | C/G | 0.408163 | 0.193609 | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71082287 | CTTAAAACAACAACT[C/G]TTTGAAAGGTCTTAG | 75763 |
rs27971842 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71082050 | CCTAAAAGATAATTC[C/T]TTGGTAATTCATGAG | 75763 |
rs27971843 | snp | C/T | 0.48 | 0.0979796 | synonymous-codon, missense, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71081963 | GAACGCATTCCAGAT[C/T]GGAGGCCATCCTTGG | 75763 |
rs27971844 | snp | A/C | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71081829 | TATGTATATGAACCA[A/C]GAAAGGTTGAACCTA | 75763 |
rs27971845 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Dcaf17 | Mm_Celera | 2:71081797 | CAGTAATTTTTCATT[A/C]ATGGAACTTTGTAAA | 75763 |
rs27971846 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Dcaf17 | Mm_Celera | 2:71081556 | TACGTAGATCCTCGG[C/T]GATGGGTGCACCTTT | 75763 |
rs27971847 | snp | A/G | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71081544 | CCCAGAGTCTTGTAC[A/G]TAGATCCTCGGCGAT | 75763 |
rs27971848 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Dcaf17 | Mm_Celera | 2:71081521 | CAAGGAGTTGACACT[G/T]TGGCTAACCCAGAGT | 75763 |
rs27971849 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71081343 | TAAGGTCTCCATTGT[A/G]CCAGACCCCATCCTA | 75763 |
rs27971850 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71081236 | AAAGCACCAACAACA[A/G]ACCCTTTGATGTCCA | 75763 |
rs27971851 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Dcaf17 | Mm_Celera | 2:71081177 | CAGTGCTAGAGCAAA[C/T]CTATTACACTATAAT | 75763 |
rs27971852 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Dcaf17 | Mm_Celera | 2:71081149 | ATGGCAACCTCACTG[C/T]AGGGCCTCCTTACAG | 75763 |
rs27971853 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Dcaf17 | Mm_Celera | 2:71081123 | GTTGTCTGTCTACAG[A/C]CACGAAAGACATGGC | 75763 |
rs27971854 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Dcaf17 | Mm_Celera | 2:71080929 | GTGAGCTACTTTTCA[A/T]GATCCATTTTCTCCT | 75763 |
rs27971855 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Dcaf17 | Mm_Celera | 2:71080925 | GTTTGTGAGCTACTT[C/T]TCAAGATCCATTTTC | 75763 |
rs27971856 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Dcaf17 | Mm_Celera | 2:71080569 | CAGTATAAACATGCT[C/T]ACATAGCTCTTTTAA | 75763 |
rs27971857 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf17 | Mm_Celera | 2:71080487 | AAGCTGACTCATTTC[C/T]AAGTGAATTAGGCAG | 75763 |
rs27971858 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Dcaf17 | Mm_Celera | 2:71080341 | ATAGTCAACAAAATA[A/G]GTTAGGAAAAAGAAG | 75763 |
rs27971859 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Dcaf17 | Mm_Celera | 2:71080214 | TCCAGCCCTTTCATC[C/T]GTTCCTAACCATTGA | 75763 |
rs27971860 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Dcaf17 | GRCm38.p3 | 2:71079736 | CAATTTGATGACTGC[A/T]GTGTGGTTAAAAGAG | 75763 |
rs27971861 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71079735 | ACAATTTGATGACTG[C/T]AGTCTGGTTAAAAGA | 75763 |
rs27971862 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf17 | Mm_Celera | 2:71079661 | AGCAGACCTTTGAGT[A/G]TCTGTTGAACTCTGT | 75763 |
rs27971863 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Dcaf17 | Mm_Celera | 2:71079633 | TTGTGTGTCTGTTGC[A/G]CTCTGTGGAGACAGC | 75763 |
rs27971864 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Dcaf17 | Mm_Celera | 2:71079586 | GATTTGGGAGGTCAT[C/T]TGCCTAAGGGAATTA | 75763 |
rs27971865 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Dcaf17 | Mm_Celera | 2:71079473 | GCTAGCCTGAGCTAC[A/G]TGAGATCTTGTCCCA | 75763 |
rs27971866 | snp | A/C | 0.487535 | 0.077957 | intron-variant | Dcaf17 | Mm_Celera | 2:71079449 | TTAATAAAAAGCCAG[A/C]AATTGAAGGCTAGCC | 75763 |
rs27971867 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Dcaf17 | Mm_Celera | 2:71078895 | TGTGTATTCCTTACT[A/T]TTGAATGAAGGTCAG | 75763 |
rs27986568 | snp | A/C | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71078204 | AGTACACTTGGTGTG[A/C]GGCTTGGGCGCAAAG | 75763 |
rs27986569 | snp | C/T | 0.497778 | 0.0332592 | synonymous-codon, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71078158 | CTTCCAAGCCATCAT[C/T]GAACAGGTAGAGGAA | 75763 |
rs27986570 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Dcaf17 | Mm_Celera | 2:71077986 | ATTTAAAGCATAAAA[C/T]ACAGGCATTCTGAAG | 75763 |
rs27986571 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Dcaf17 | Mm_Celera | 2:71077883 | ATTGATGCTCCAGTC[C/T]GAGGCTTGCTGCTTG | 75763 |
rs27986572 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Dcaf17 | Mm_Celera | 2:71077729 | TGGATATACCTGATA[C/T]TCATCTAAAATTACA | 75763 |
rs27986573 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf17 | Mm_Celera | 2:71077107 | CACGAGATTCAAAGA[C/T]AGAACATTTAGGGAA | 75763 |
rs27986574 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Dcaf17 | Mm_Celera | 2:71076900 | AATATACAGGGGTGA[A/G]GCCCTCAAGCAGTTG | 75763 |
rs27986575 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71076854 | TGTGATGCAGGATTA[A/G]AGCACGTCTTTCACT | 75763 |
rs27986576 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71076823 | ATAGTCGGTTGAGGG[A/T]TTTGGCTTTGATTAA | 75763 |
rs27986577 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Dcaf17 | Mm_Celera | 2:71076278 | CTTTAAAAGTGGTTG[C/T]TCTGTGGGAAACCAT | 75763 |
rs27986578 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Dcaf17 | Mm_Celera | 2:71076168 | TCTTTCTAAGTCATA[C/G]AGTTTGGGTTTTTAT | 75763 |
rs27986579 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Dcaf17 | Mm_Celera | 2:71075725 | GTGCTCTACCATACT[A/G]CAATTACTTAATTGC | 75763 |
rs27986580 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71075249 | CTATGTTTGTAAGAA[C/G]CTGGAAGATTAGTGA | 75763 |
rs27986581 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Dcaf17 | Mm_Celera | 2:71074830 | TCCTGTGGTTTTGAT[A/T]GGTAGTCTTGATAGT | 75763 |
rs27986582 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Dcaf17 | Mm_Celera | 2:71074768 | GGTCTCTAGGGCTTT[A/G]AACATCACATTCTGC | 75763 |
rs27986583 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71074668 | GAAGCAGTAGTTCTT[G/T]GTGAAGATATACAAA | 75763 |
rs27986584 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71074052 | CCTTCTCGGTCCTTA[C/T]GTATGCCACTGAGCC | 75763 |
rs27986585 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71074014 | ATTCCTTTACCCTCT[A/G]CATTCTGTTCCTCTC | 75763 |
rs27986586 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71073242 | TGGCATTTGCACACT[C/T]GTGAAAGCAAGTGCT | 75763 |
rs27986587 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71073203 | GCGGCTCGCCAGGTC[C/G]GCAGCATTTGGCACG | 75763 |
rs27986588 | snp | C/T | 0.231111 | 0.249285 | missense, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71073189 | ACAAAGGCTCCGCAG[C/T]GGCTCGCCAGGTCCG | 75763 |
rs27986589 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71073100 | ATCCAAATGTTAAAT[A/T]CCTCTCCATTCCTTC | 75763 |
rs27986590 | snp | A/C | 0.495 | 0.0497494 | intron-variant | Dcaf17 | Mm_Celera | 2:71073063 | AAAGTGTAATGTTTC[A/C]ATTTTGAGTCTAAGG | 75763 |
rs27986591 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Dcaf17 | Mm_Celera | 2:71072998 | AAAGAGTCACAGGCC[A/G]GATTTTATCCCCAAA | 75763 |
rs27986592 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Dcaf17 | Mm_Celera | 2:71071954 | TAACATTCTACTAAG[A/G]GGAAGATCAAGCTTT | 75763 |
rs27986593 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71071889 | AAATGCTACAGATGA[A/G]TTCCTCCAATGTTCT | 75763 |
rs27986594 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71071856 | CTGAATCGGCTGAGC[A/G]TCAGGCCTTGCATTG | 75763 |
rs27986595 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71071759 | CTCCAACCACGGCTC[C/T]TCTTCCAAGAATTTG | 75763 |
rs27986596 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Dcaf17 | Mm_Celera | 2:71063704 | TTATTTATGTACAAA[A/G]ATTCCATATAAGTAA | 75763 |
rs27986597 | snp | C/G | 0.465374 | 0.126941 | intron-variant | Dcaf17 | Mm_Celera | 2:71063601 | TCCCCAGTTTTCCCT[C/G]TGTATTTTATGATCC | 75763 |
rs27986598 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71063334 | GTTTTCACACCCTGG[C/T]TTAGTTTGTTTGTTT | 75763 |
rs27986599 | snp | C/T | 0.497778 | 0.0332592 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71063199 | TAACAGGCACAGCCT[C/T]GTCTGTCCCACTTTC | 75763 |
rs27986600 | snp | A/C | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71063147 | ATGATAATGATGATA[A/C]AATGTAAACGCATTA | 75763 |
rs27986601 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062853 | TTTCCCTTCTGCAGT[C/T]GAGCTGTACTAGTGG | 75763 |
rs27986602 | snp | A/G | 0.473373 | 0.11227 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062657 | ACAGGGCCTGCCTGA[A/G]AAACAACAAAAATAA | 75763 |
rs27986603 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062647 | TCTGCACTGCACAGG[A/G]CCTGCCTGAGAAACA | 75763 |
rs27986604 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062640 | TTCCCAGTCTGCACT[A/G]CACAGGGCCTGCCTG | 75763 |
rs27986605 | snp | A/G | 0.46281 | 0.131194 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062515 | AAATCTACATGAAAT[A/G]ACACATAAGTCATGT | 75763 |
rs27986606 | snp | C/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062459 | GTTTTAAATGTCTCT[C/G]TAATGGGCTAAATAG | 75763 |
rs27986607 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062227 | GCAGTCCTGAAAAAA[C/T]AAAGTTAACCTACTC | 75763 |
rs27986608 | snp | A/C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Dcaf17 | GRCm38.p3 | 2:71061877 | AGAGAAGAGAACTTC[A/C/T]AGTCTGTAACCCAGA | 75763 |
rs27986609 | snp | G/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71061875 | CAAGAGAAGAGAACT[G/T]CTAGTCTGTAACCCA | 75763 |
rs27986610 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71061689 | GCTGTTTCTAATACT[A/G]CCTGCATGCACAGTG | 75763 |
rs27986611 | snp | A/G | 0.497778 | 0.0332592 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71061668 | TCCTCCTCAGTCTTT[A/G]ACATGGCTGTTTCTA | 75763 |
rs27986612 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71061649 | CCAAGGATGCTTGTC[C/T]GTCTCCTCCTCAGTC | 75763 |
rs27986613 | snp | A/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71061621 | GAAAAATAAATACGG[A/G]ACATTGAAAGTTCCA | 75763 |
rs27986614 | snp | C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71061537 | TGTTGCCCTGGCACG[C/T]GCCCTCCTGCACACT | 75763 |
rs27986615 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71061519 | GTCATGCCGTGAGGC[C/T]GGTGTTGCCCTGGCA | 75763 |
rs27986616 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71061505 | GCTACATAGTGAAAG[C/T]CATGCCGTGAGGCCG | 75763 |
rs27986617 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71060662 | TCATCTTGATTATGG[C/G]ACACACACACTATAT | 75763 |
rs27986618 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71060266 | GTCTGAGCAAAGACT[A/G]CCTCAGTTTAAAACA | 75763 |
rs27986619 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71060238 | CTGGGTGCTACAGGC[A/G]TGCAAAAGAAATGTC | 75763 |
rs27986620 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Dcaf17 | Mm_Celera | 2:71059783 | GCAAGAGGATAAACT[C/T]AGTGAATTCAACAGA | 75763 |
rs27986621 | snp | C/G/T | 0.493827 | 0.0552116 | intron-variant | Dcaf17 | GRCm38.p3 | 2:71058900 | TAGTTTGGGGGATGG[C/G/T]GGCCTGAGAGAGGGG | 75763 |
rs27986622 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf17 | Mm_Celera | 2:71058483 | CATTGATTGCTGTCG[C/T]AGTGATAAATGATGC | 75763 |
rs27986623 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Dcaf17 | Mm_Celera | 2:71058433 | AAGTCAGAGACAGTT[A/G]TTTTGATTTTAAAAA | 75763 |
rs27986624 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Dcaf17 | Mm_Celera | 2:71058268 | CCTTTCATTTCTTCA[A/G]TTTTCCAGAAGGCAG | 75763 |
rs27986625 | snp | C/T | 0.493827 | 0.0552116 | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71057187 | TTTCTGTGTGCCAAG[C/T]TTCAGTGGTGTTGTT | 75763 |
rs27986626 | snp | A/G | 0.475309 | 0.108333 | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71057114 | TCACCTGGATTAAGG[A/G]ATTATGGAATTGCCG | 75763 |
rs27986627 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71057068 | GTCAGACTGAAGAGA[A/C]CGACACAGTGAATTG | 75763 |
rs27986628 | snp | C/T | 0.475309 | 0.108333 | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71056902 | TCAGAGTCCAGAAAA[C/T]GGGTTGTGAAATAAT | 75763 |
rs27986629 | snp | C/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71056895 | TTAAAGATCAGAGTC[C/G]AGAAAATGGGTTGTG | 75763 |
rs27986630 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71056833 | ACAAAATTATAGCAC[A/G]GGCAAAATAATACGT | 75763 |
rs27986631 | snp | A/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71056607 | TCAGCAGGTAAATTC[A/T]TGGTGATGATTTTTT | 75763 |
rs27986632 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71056542 | TCATTCCAAGTCACC[C/T]ATAGCCTATGAGAGA | 75763 |
rs27986633 | snp | A/G | 0.487535 | 0.077957 | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71056454 | GTTCCATAGCAGGGG[A/G]CTGAGTTCTTTCCTA | 75763 |
rs27986634 | snp | C/T | 0.473373 | 0.11227 | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71056353 | CCAACTAAACCGACA[C/T]CTATGGGCAGAGGGA | 75763 |
rs27986635 | snp | C/T | 0.497778 | 0.0332592 | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71056296 | AGTTTTTAAAAAGCT[C/T]CTTTTGCCTTCCTGC | 75763 |
rs27986636 | snp | A/C | 0.124444 | 0.216185 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71055984 | TGGGCCCTGCGGACC[A/C]CTAGTCTCCATGGGC | 75763 |
rs27986637 | snp | A/G | 0.132653 | 0.220748 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71055980 | CTCCTGGGCCCTGCG[A/G]ACCCCTAGTCTCCAT | 75763 |
rs27986638 | snp | A/G | 0.475309 | 0.108333 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71055866 | TGTCGCTACCTCTTG[A/G]TCTCTGCCCCGAGTC | 75763 |
rs27986639 | snp | C/T | 0.475309 | 0.108333 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71055840 | TTCTGTTCCTTTGCG[C/T]CAAATCCGTGTGTCG | 75763 |
rs27986640 | snp | A/G | 0.132653 | 0.220748 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71055804 | CGAGAGCAGAAAGAA[A/G]GGCCAGGAAGGCGCC | 75763 |
rs27986641 | snp | A/C | 0.456747 | 0.140554 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71055757 | CGGGAGAGGGAGTGG[A/C]TACGGAGGGCCGCGA | 75763 |
rs27986642 | snp | G/T | 0.46875 | 0.121031 | upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71055709 | CTGAAAAAGAAGCCA[G/T]AGGGGCGGAAAAGGC | 75763 |
rs27986643 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, utr-variant-5-prime | Dcaf17, Mettl8 | Mm_Celera | 2:71055589 | CCCGACCCACTGCGC[A/G]GCCCTACGGCGCAGC | 75763 |
rs27986644 | snp | A/T | 0.493827 | 0.0552116 | upstream-variant-2KB, utr-variant-5-prime | Dcaf17, Mettl8 | Mm_Celera | 2:71055478 | AGGGCAGAAAGGGAC[A/T]GCTTCCTGGGACACA | 75763 |
rs27986645 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71055246 | TCAATCCTACTTTGA[C/T]GGGAAAAACAGCAAC | 75763 |
rs27986646 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71055180 | AATTACCACAAAACC[A/G]GTCAGGGTCCCCGCT | 75763 |
rs27986647 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054996 | CAGTTACGGAAATTT[C/T]TAGTATGTTAGTAAT | 75763 |
rs27986648 | snp | A/C | 0.489796 | 0.070696 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054991 | GTATACAGTTACGGA[A/C]ATTTTTAGTATGTTA | 75763 |
rs27986649 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054562 | TTTCTGGGTTCCAGC[A/G]TTTCAGTGACAGCTG | 75763 |
rs27986650 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054431 | AACCAAAGCTCAGCC[A/G]TGGTGGGAGAGCACA | 75763 |
rs27986651 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054375 | GTGGTAATAGTGGAG[C/T]ATAGTGGCATCTTAG | 75763 |
rs27986652 | snp | A/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054330 | GCGGAAGGTATGATC[A/T]CAATATGCCCACTAC | 75763 |
rs27986653 | snp | A/C | 0.391111 | 0.206368 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054210 | TGGTCCAAACCAAGA[A/C]AGACAGCGCCATTAC | 75763 |
rs27986654 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054149 | CTCAAGCGCACAGAG[C/T]TTCCAGAGGTTAAGC | 75763 |
rs27986655 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054069 | GAAAAACACTGAGAG[A/G]CAACTGGCCTTGAAG | 75763 |
rs27986656 | snp | A/G | 0.497778 | 0.0332592 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054029 | ATGATTTAGGGGCCA[A/G]GCTTGATGCCTCGTG | 75763 |
rs27986657 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71053985 | AGCTCACTGGCTGTC[A/G]ACTGTGAGGAAAGAA | 75763 |
rs27986658 | snp | A/G | 0.408163 | 0.193609 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71053970 | TGCAGTCCCTCAGCC[A/G]GCTCACTGGCTGTCG | 75763 |
rs27986659 | snp | C/T | 0.497778 | 0.0332592 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71053881 | TAGGGATCCCAGTGG[C/T]AAGATCAATAGCACA | 75763 |
rs27986660 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71053789 | GGCATAAAACTACTG[A/G]GATGAAAAGACTGGA | 75763 |
rs29498354 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71087484 | CACCCTGCAGGCAGG[A/G]TGGGGAAGGGAGTGT | 75763 |
rs29501766 | snp | A/T | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71106463 | ATCTGCATTGTCAGA[A/T]GATCAGCAGTTCAGT | 75763 |
rs29502435 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B, intron-variant | Dcaf17 | Mm_Celera | 2:71096051 | GTTGTTCTTTATTTT[C/T]TTAACGTTTGCTCAG | 75763 |
rs29522475 | snp | A/G | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71078875 | TGTGTGTGTGTGTGT[A/G]TGTGTATTCCTTACT | 75763 |
rs29525936 | snp | C/T | 0.444444 | 0.157135 | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71082881 | CAAAGATTCTTACCC[C/T]TTCCTGACCCATGCT | 75763 |
rs29553260 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf17 | Mm_Celera | 2:71078397 | CTCGGTCATGTACAT[A/G]TAAATTTTATTTTTT | 75763 |
rs29554949 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71058989 | TGTTCAAAGATAGTA[A/G]AAATAGACATATATT | 75763 |
rs29572441 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf17 | Mm_Celera | 2:71077991 | AAGCATAAAATACAG[A/G]CATTCTGAAGATCAG | 75763 |
rs29573103 | snp | C/G | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71061231 | AGCTTGAACCTTGGA[C/G]TTCATCCACCCCTGA | 75763 |
rs29573601 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcaf17 | Mm_Celera | 2:71081465 | GGAAGGTCTCTCTGC[C/T]TATAAAAATTTATTA | 75763 |
rs29578455 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71108699 | AGAGCCAGCACTCTG[A/T]ACTGCTGAGTCAGTT | 75763 |
rs29579868 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71092045 | GGCTACACAGAGAAA[C/T]TTTGTCTGGGGTAAT | 75763 |
rs29587269 | snp | G/T | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71083752 | GCACCACCACACTTG[G/T]CTTTTTCCTTTATTT | 75763 |
rs29620205 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71096370 | TTACTCACATGACCA[C/T]CGGAGCCTGACCAAG | 75763 |
rs29622163 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71056380 | GGGAGAAAAAAAAAA[A/G]AAAAAAAGGAGAAAC | 75763 |
rs29673174 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71095730 | CCATGCTGGAACATC[A/G]CTCGTTCATTACGTT | 75763 |
rs29675512 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71080654 | CCACAATAGGGTGCT[A/G]GATTCCCTGGAACTT | 75763 |
rs29715393 | snp | C/T | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71077313 | GTGTGCTCATGAGAA[C/T]ATGAGTTTAGATTCC | 75763 |
rs29717473 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71101743 | TTACCTGGCCAGGCT[G/T]TTTGGGACCTATGTG | 75763 |
rs29717712 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71080687 | GTTGTAGATAATTAT[A/G]ATGTAAGTGCTGGGA | 75763 |
rs29811504 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf17 | Mm_Celera | 2:71072699 | TTCTTTTGTGATTGG[A/G]TTACCTCACTAAGGA | 75763 |
rs29824305 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091721 | GACAATGAAGAATTC[C/T]GTGTCAGCTTGGCAT | 75763 |
rs29859122 | snp | A/T | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71072593 | ATTGGTCTTCCCTCT[A/T]CTTGATTTTCTTGTG | 75763 |
rs29872697 | snp | A/T | 0.32 | 0.24 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091812 | AGAGCAACAGGCCAT[A/T]CTTGATTCAAGTTTA | 75763 |
rs29873717 | snp | A/G | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71077314 | TGTGCTCATGAGAAC[A/G]TGAGTTTAGATTCCT | 75763 |
rs29883191 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71107436 | TTTTAACCAATAACA[A/G]CTCCTCTTCCTCATT | 75763 |
rs29884207 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf17 | Mm_Celera | 2:71058037 | CAGAGATTGCCTTCC[A/G]AGTCAGAGCAGCAGG | 75763 |
rs29909187 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71102551 | CTGTAATGGAGTCCA[A/G]TGCCCTCTTCTGGTG | 75763 |
rs29909578 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71059173 | ATTTCTCCATCACTA[C/T]TCATCTCTGAAGAAA | 75763 |
rs29958194 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf17 | Mm_Celera | 2:71076394 | CAAGACAAATCTATT[A/G]AAACATTTCCTATTC | 75763 |
rs29966080 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcaf17 | Mm_Celera | 2:71074321 | TATATCTTGCCCAGT[C/T]ATCTCAACAGCATGA | 75763 |
rs32846025 | snp | A/T | 0.32 | 0.24 | intron-variant | Dcaf17 | Mm_Celera | 2:71074320 | CTATATCTTGCCCAG[A/T]CATCTCAACAGCATG | 75763 |
rs32867244 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71095116 | GCCACAAGTAAAGGC[C/T]AGCCTGGGCAGCTTA | 75763 |
rs32902003 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf17 | Mm_Celera | 2:71058057 | AGAGCAGCAGGGGAC[A/G]GATCCTGGCACTCAG | 75763 |
rs32902156 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71075673 | TTGGGTTCAGAGATC[C/T]ACCAGTTTCTGCCTC | 75763 |
rs32932920 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Dcaf17 | GRCm38.p3 | 2:71061594 | CCCGAGAAGCTAGGA[A/G]TGATTGGTCTGGGGA | 75763 |
rs32961586 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71077793 | GAAGTAGAATCTGTA[A/G]TTACTGTGTATTGAC | 75763 |
rs32976334 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71080658 | AATAGGGTGCTGGAT[C/T]CCCTGGAACTTGAGT | 75763 |
rs32981075 | snp | A/T | 0.32 | 0.24 | intron-variant | Dcaf17 | Mm_Celera | 2:71084854 | GTAGTTCATACTGGC[A/T]GCTAGTTTTGTGTAG | 75763 |
rs32982558 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71057708 | GGGGCTGTTTCATGG[C/T]CTGCTTCTTTTCCCA | 75763 |
rs33014716 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71102205 | GAGTTCCAGGCCAAC[A/C]AGGGCCATATAGCAA | 75763 |
rs33015179 | snp | A/C | 0.32 | 0.24 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091822 | GCCATACTTGATTCA[A/C]GTTTAAGGTTAAAAT | 75763 |
rs33038588 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091800 | AAGCATAGGAGAAGA[A/G]CAACAGGCCATACTT | 75763 |
rs33067506 | snp | A/G | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71077310 | GCTGTGTGCTCATGA[A/G]AACATGAGTTTAGAT | 75763 |
rs33092258 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71056371 | ATGGGCAGAGGGAGA[A/G]AAAAAAAAAAAAAAA | 75763 |
rs33110350 | snp | G/T | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71079953 | TGTGAGCCACCATGT[G/T]GTTGCTCGGATTTGA | 75763 |
rs33138099 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71097046 | CCATCCATTTACCTG[A/C]AATTTTCATGATGTC | 75763 |
rs33141794 | snp | G/T | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant | Dcaf17 | Mm_Celera | 2:71099108 | CACACCACCATACCA[G/T]GCTTACTTAATAAAC | 75763 |
rs33172954 | snp | A/G | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71101385 | AGGAGAGATGGTCCT[A/G]CTGTATCAGTGATGT | 75763 |
rs33174507 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71099791 | TAGGCTACACTTACA[A/G]TCATAAATAAGAAAA | 75763 |
rs33222051 | snp | G/T | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71079974 | TCGGATTTGAACTCA[G/T]AACCTTCGGAAGAGC | 75763 |
rs33238724 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71079739 | TTTGATGACTGTAGT[C/G]TGGTTAAAAGAGCCA | 75763 |
rs33251435 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf17 | Mm_Celera | 2:71081819 | CTTTGTAAATTATGT[A/G]TATGAACCAAGAAAG | 75763 |
rs33251586 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71078624 | TTAAGAAAGTAAGTG[C/T]TCATATAAATAGTCA | 75763 |
rs33274860 | snp | C/T | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71083705 | CAGAGCTCTGCCTGC[C/T]TCTGCCTCCAAAGTG | 75763 |
rs33280988 | snp | A/C | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090932 | TGTCTCTTTCCCAGC[A/C]CTGGGACTAAAGGCA | 75763 |
rs33283568 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71078600 | GCTGCTATACAGTAT[C/T]TTTTCTCCTTAAGAA | 75763 |
rs33319393 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71101915 | TGATGGAGAAGATCT[C/T]TGATCTTGTTGTGGC | 75763 |
rs33326358 | snp | C/T | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Dcaf17 | GRCm38.p3 | 2:71106488 | TTCAGTTTACAGGAG[C/T]GAGCAGCAGCGGCTT | 75763 |
rs33330437 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf17 | Mm_Celera | 2:71081482 | ATAAAAATTTATTAG[A/G]CCTGATTAGCCGCTA | 75763 |
rs33342584 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71101800 | CACAAAATCCACATC[C/G]TAGATTGACAGGATA | 75763 |
rs33344783 | snp | C/T | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71083615 | AAACAGGCGGTGTTT[C/T]TTTCTTTCTCTCCCA | 75763 |
rs33347754 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71080705 | GTAAGTGCTGGGAAC[C/T]GAACATGAGTTTATT | 75763 |
rs33350050 | snp | G/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062949 | AGAACCCACAGAAAG[G/T]CAGGAGAGCTGAGCA | 75763 |
rs33359538 | snp | A/T | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71099719 | CAGCCTCTGCCTTCC[A/T]CTGCAGGGATCAGGT | 75763 |
rs33379805 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71057895 | GGGCCCTGTTACTCT[A/G]CACTGTAGTTATACC | 75763 |
rs33412385 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71095559 | AATGAAATACACATA[C/T]ATTGTATAATTTTGC | 75763 |
rs33436379 | snp | G/T | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71107743 | ACAGAGCAACTCTCA[G/T]CTTCCTTCCCTGATG | 75763 |
rs33496437 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71097007 | GTGTCTGGGTTACCT[C/T]ACTCAAAGTGGCCTT | 75763 |
rs33501938 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71087498 | GATGGGGAAGGGAGT[A/G]TGTGGTCCACTCAGT | 75763 |
rs33509961 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcaf17 | Mm_Celera | 2:71072703 | TTTGTGATTGGATTA[C/T]CTCACTAAGGATGAT | 75763 |
rs33545959 | snp | G/T | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71080174 | CTGGAAGAGCAGTCA[G/T]TGCTCTTACTCCCTG | 75763 |
rs33565181 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71080228 | CTGTTCCTAACCATT[A/G]AACTGAGCTTTTTTT | 75763 |
rs33574971 | snp | C/G | 0.32 | 0.24 | intron-variant | Dcaf17 | Mm_Celera | 2:71085068 | AGCCTAGGCAACTTT[C/G]TGAGACCTCTTACTA | 75763 |
rs33627167 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf17 | Mm_Celera | 2:71102491 | ACTGTTCTTCCAGAG[A/G]TCCTGAGTTCAATTC | 75763 |
rs33632118 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71072256 | CTATAGGGTTGCAGA[C/T]CCCTTCAGCTCCTTG | 75763 |
rs33633102 | snp | A/G | 0.5 | 0 | intron-variant | Dcaf17 | Mm_Celera | 2:71087793 | AAGGGGTGCACCACC[A/G]TTGCATTTGAGAGCA | 75763 |
rs33658661 | snp | A/T | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant | Dcaf17 | Mm_Celera | 2:71099107 | ACACACCACCATACC[A/T]TGCTTACTTAATAAA | 75763 |
rs33692742 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf17 | Mm_Celera | 2:71076728 | ATTAAGTAATTATAT[A/G]TGTATTACATTCTTC | 75763 |
rs33696218 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71077804 | TGTAGTTACTGTGTA[C/T]TGACAAAGTTGTACA | 75763 |
rs33731519 | snp | C/G | 0.375 | 0.216506 | intron-variant | Dcaf17 | Mm_Celera | 2:71087303 | TTCTCCCCACCCCCG[C/G]CCCCCCATCAGAAGG | 75763 |
rs45674129 | snp | A/G | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054658 | CGTATGCTATAAGCA[A/G]GTCATGAAATATCAG | 75763 |
rs45705066 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110693 | ATTTGCCTCGAAAAG[C/T]ACCCGGAAATATATA | 75763 |
rs45750667 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71087434 | ACCAACAGTCCATTT[A/C]CATTCAGTTTAATGC | 75763 |
rs45808314 | snp | C/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110539 | CTTATTTAAAAAACA[C/G]CTTTAAAATAGAGAA | 75763 |
rs45841217 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112099 | AAAATGCTTTCCCTG[G/T]CTCTGTTTTGTTCAC | 75763 |
rs45846563 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060065 | ATGTGAGGGTAGGAA[C/T]CAAACTTGAGTCCTC | 75763 |
rs45865212 | snp | A/T | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71061983 | AGCTATAATTTTTTT[A/T]AACTATCACTCCCCC | 75763 |
rs45880828 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105587 | CTGGAAAGACACACA[A/G]TACAGCTGACGAGAC | 75763 |
rs45936855 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71103177 | CCCCGTCCTTGGGGC[A/G]GGGGTGGCAATTGTT | 75763 |
rs45948711 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71079961 | ACCATGTTGTTACTC[A/G]GATTTGAACTCATAA | 75763 |
rs46117124 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110163 | CCTTGAGAGGCATGC[A/G]TCATAGGTTTTCCAG | 75763 |
rs46161502 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111158 | GCAGCCAACAGCCCG[G/T]CTGAGGCTCTGGCCA | 75763 |
rs46164340 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110863 | GAATCATGGTCATTT[C/T]CTTGCTGTAAGCACT | 75763 |
rs46230967 | snp | A/G | | | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71082393 | CTTCAAACTCAGTAC[A/G]TAGGCAAGACTGGCC | 75763 |
rs46267747 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105592 | AAGACACACAATACA[A/G]CTGACGAGACCATGG | 75763 |
rs46392344 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111575 | AGACCAGGCTGGCCT[C/T]GAACTCAGAAGCCGC | 75763 |
rs46442177 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090356 | CACACTTGTAATATC[A/G]GTGCATGGCGGGTAG | 75763 |
rs46580233 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104867 | AATCTGAGCACAACA[C/T]GGTTGTGTTTGAATG | 75763 |
rs46619242 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111802 | aaattcaaagctatc[A/G]gaaaccagtcacatt | 75763 |
rs46626465 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Dcaf17, Mettl8 | Mm_Celera | 2:71055409 | AACGCCCCTCTGGAC[A/G]CGTGGCCAGAGCCTT | 75763 |
rs46653667 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098089 | CCAGTACCATATTGT[C/T]TTTATTACTATGGTT | 75763 |
rs46784422 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112082 | AGAAGTTAATACAAA[C/T]AAAAATGCTTTCCCT | 75763 |
rs46799110 | snp | A/G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060124 | GAACCATCTCTCTTG[A/G/T]TTTTTTTTTTAACAT | 75763 |
rs46817035 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71100460 | ATGGTCATATAATCA[A/C]CAAGGTTGTCCCTAC | 75763 |
rs46921818 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71097898 | CAAGGTGATGGATGG[A/G]GATATAATTCCATTC | 75763 |
rs46937110 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71063916 | GGCGTATGTCTTTAA[C/T]CCCAGCACTCAGGAG | 75763 |
rs46958073 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104527 | TGCTGGGACTTGAAC[A/T]CCGGACCTTCGGAAG | 75763 |
rs46995759 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71063923 | GTCTTTAACCCCAGC[A/G]CTCAGGAGACAGGAG | 75763 |
rs47031247 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059759 | ATCTGTATATTATCT[C/T]TCTTAAGAGCAAGAG | 75763 |
rs47047671 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104322 | GATACTGAGAGATGC[C/T]CCTCAGCCTTTTTTT | 75763 |
rs47063775 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71103744 | ATATCAGACATCCTG[A/C]ATATCAGATATTGAT | 75763 |
rs47183559 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110687 | TTAGAAATTTGCCTC[A/G]AAAAGTACCCGGAAA | 75763 |
rs47233194 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090287 | TTAATTAGTAAGGCT[A/G]GGAGAGAAAAACAAA | 75763 |
rs47240697 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098103 | TTTTTATTACTATGG[C/T]TCTAGTATAACTTGA | 75763 |
rs47371866 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71087433 | AACCAACAGTCCATT[A/T]CCATTCAGTTTAATG | 75763 |
rs47409675 | snp | C/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091712 | CAGAGGCAGGACAAT[C/G]AAGAATTCCGTGTCA | 75763 |
rs47526989 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104880 | CACGGTTGTGTTTGA[A/T]TGGGAAACAGAAGCA | 75763 |
rs47578217 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71057985 | CAACAACTCATGGCT[G/T]GGGCTGGATGAAAAC | 75763 |
rs47819114 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104487 | GTCAGATCTCGTTAC[A/G]GATGGTTGTGAGCCA | 75763 |
rs47889411 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060825 | GCTCTTCACCTAGGG[G/T]TGGGGCTTTGTGAGA | 75763 |
rs47951148 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71097518 | TTTGAGAAGTCTGTT[C/T]AGCTCCCAGGCCCAT | 75763 |
rs48069709 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112812 | CGAGCCACGTTATTT[C/T]GGAACAAAAGTAAAG | 75763 |
rs48158858 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71063998 | ACAGCCAGGGCTACA[C/T]AGAGAAACCCTGTCT | 75763 |
rs48183526 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71100689 | TGGCACCATGGACAC[A/G]CACCATGGGACCCTA | 75763 |
rs48188301 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105605 | CAGCTGACGAGACCA[C/T]GGACCTTACTCAGGT | 75763 |
rs48220825 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71097626 | AAACGTCTGCCAGGT[A/G]TACGGTTGGCAGAGA | 75763 |
rs48421748 | snp | C/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110893 | TCTCTTCCTTATGGT[C/G]TGGTTTTCTCACCTA | 75763 |
rs48507394 | snp | A/G | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71053919 | AGCATTCAGAAGGCC[A/G]GGTAAGAATGGGGAC | 75763 |
rs48540613 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71085900 | CAGTGGCTTCTTGCT[A/G]TTCTCTTTGCCTATG | 75763 |
rs48624974 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71088271 | TTTCAGAAGTGATAG[A/G]ATAATTAAATTTAGA | 75763 |
rs48665659 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71089191 | GCTGTGCAAATGTGA[A/G]AACTTTGGGTTTCGG | 75763 |
rs48670866 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112090 | ATACAAACAAAAATG[C/T]TTTCCCTGTCTCTGT | 75763 |
rs48852097 | snp | A/G | | | intron-variant, missense | Dcaf17 | Mm_Celera | 2:71088593 | AGTCCAGATTCACCT[A/G]TGCTGTGACCACACG | 75763 |
rs48871643 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111157 | AGCAGCCAACAGCCC[G/T]GCTGAGGCTCTGGCC | 75763 |
rs48917347 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112406 | CAGGGCTTTGAGTTG[G/T]CCCACCCTAACATCC | 75763 |
rs48927072 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090339 | AGCCAGGTATGGTGG[A/C]ACACACTTGTAATAT | 75763 |
rs48927215 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104663 | TGAGTAGGCTTCAAG[G/T]GGGGAGAGGAGGAAA | 75763 |
rs48936201 | snp | A/C | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054690 | GGGGGAAAAAAAAAA[A/C]CTCCAACAAAACAAC | 75763 |
rs49085567 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110854 | CTTGAGTTTGAATCA[C/T]GGTCATTTCCTTGCT | 75763 |
rs49254357 | snp | C/T | | | downstream-variant-500B, intron-variant | Dcaf17 | Mm_Celera | 2:71095895 | tataggtaatatgta[C/T]atatatttgtcttta | 75763 |
rs49288411 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059557 | GTACACCACCACGCC[C/T]GGCTTTTAAATGCTA | 75763 |
rs49310338 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104016 | ACCACCCAATTCAGG[G/T]AGAGATGGGATATGT | 75763 |
rs49331745 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104391 | ATCAGAAACAATGTT[C/T]CATTTTATTTTTTTT | 75763 |
rs49412743 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060796 | TCTCTCTTAGAAGCC[A/G]TTAATTGCCTATAGC | 75763 |
rs49502503 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71089189 | TTGCTGTGCAAATGT[A/G]AGAACTTTGGGTTTC | 75763 |
rs49600103 | snp | C/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71102998 | ATTCCTACAGAAACA[C/G]TCTCCATCTTCCTCC | 75763 |
rs49801988 | snp | G/T | | | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71088612 | TGTGACCACACGAAA[G/T]AAGTTATTGTCCAAT | 75763 |
rs49847076 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104998 | CTGGGAGAGAAGAGT[C/T]CAAGGCTGTGATCTG | 75763 |
rs49992192 | snp | A/T | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054130 | GAAGCAAGTAAACAG[A/T]CTTCTCAAGCGCACA | 75763 |
rs49995660 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71103853 | TGTATTAAAGGGTCG[C/T]AGCATTAGGAAGGTT | 75763 |
rs50074822 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112294 | AACATTTAAGTGATG[G/T]GCGCCTGCCCCTTGC | 75763 |
rs50195531 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090872 | TTCACTAGGGCCTGC[A/G]GCTTACTGATACTGC | 75763 |
rs50207969 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71057988 | CAACTCATGGCTTGG[A/G]CTGGATGAAAACAGG | 75763 |
rs50272754 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098032 | AGTAGTCATGTTTGG[A/G]TCTTTGATTTTGTTC | 75763 |
rs50321997 | snp | A/G | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71081576 | GGTGCACCTTTTGTT[A/G]TATATCTGCCTCCCT | 75763 |
rs50357650 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71087456 | GTTTAATGCTTCCCC[G/T]GCCCAGGGCAGGCAC | 75763 |
rs50500653 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112557 | TATTGATAGTGTAGC[A/G]GACTCACTGCAATGA | 75763 |
rs50515242 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71101121 | CTCGTTGGAAATTTT[C/T]CCCCCCATTTCTTTG | 75763 |
rs50524196 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098194 | CATGTTATTTTGTGG[C/T]TCCATCTTAATGGTG | 75763 |
rs50577860 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71103986 | CACATTCCAATAGGG[G/T]TTGCCAGTTACAAGA | 75763 |
rs50627451 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71079392 | GAACACTAACTAAAC[A/G]AAATTCACTTATAAT | 75763 |
rs50640456 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111923 | TCTCAGCAGTAATTA[A/G]TGTTGATTTGAAAAA | 75763 |
rs50647880 | snp | G/T | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054141 | ACAGTCTTCTCAAGC[G/T]CACAGAGTTTCCAGA | 75763 |
rs50649306 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110162 | GCCTTGAGAGGCATG[C/T]ATCATAGGTTTTCCA | 75763 |
rs50700608 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104651 | AATAGTCAACTATGA[A/G]TAGGCTTCAAGTGGG | 75763 |
rs50779780 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098097 | ATATTGTTTTTATTA[C/T]TATGGTTCTAGTATA | 75763 |
rs50905197 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104869 | TCTGAGCACAACACG[A/G]TTGTGTTTGAATGGG | 75763 |
rs51027554 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104313 | TTTGAGTCAGATACT[A/G]AGAGATGCCCCTCAG | 75763 |
rs51034420 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71108858 | AAACAGATTGTTTCA[G/T]TAACATTCTGGGTAG | 75763 |
rs51059971 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71106267 | CTCATCTTTATAAGT[C/T]ACATTGGATGAACAG | 75763 |
rs51090837 | snp | C/G | | | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71088693 | GTACCTACCAGCCGG[C/G]CGTGGTGGCGCACGC | 75763 |
rs51094595 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104426 | ATTTATTTATTCATT[A/G]TATGTAAGTACACTG | 75763 |
rs51105575 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098058 | TGTTCCACTCATCTA[C/T]GTTTCTGGTTTTGTA | 75763 |
rs51120916 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112323 | GCCTGGGCAAAGTGG[A/G]AGAGCTAGCCTGGGG | 75763 |
rs51126765 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71089224 | CCCAGAACCCACCAC[A/C]TAAATGCTGGCAGGT | 75763 |
rs51342598 | snp | C/T | | | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71088607 | TATGCTGTGACCACA[C/T]GAAATAAGTTATTGT | 75763 |
rs51451631 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71089207 | AACTTTGGGTTTCGG[A/T]CCCCAGAACCCACCA | 75763 |
rs51467030 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71053906 | AGCACAGGAAGGGAG[C/T]ATTCAGAAGGCCGGG | 75763 |
rs51517430 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71089250 | CAGGTGTGTCAGCCC[A/G]ACTTAGAAGTGAAGA | 75763 |
rs51721858 | snp | A/G | | | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71088848 | AAAAAAGAAAGAAAG[A/G]GTACCTACCATCTTA | 75763 |
rs51724345 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111628 | GGGATTAAAGGTGTG[C/T]GCCACCACGCCCGGC | 75763 |
rs51731259 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71100614 | GATACTGCCTGCTGA[A/G]TGAGGAAGCTCAAAA | 75763 |
rs51741194 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110698 | CCTCGAAAAGTACCC[A/G]GAAATATATAAAGAT | 75763 |
rs51753813 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090082 | GAACTCTTACCACAT[A/G]TGGTAGAAAGGACTC | 75763 |
rs51785630 | snp | C/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111510 | TGTTTTTTTGTTTTT[C/G]GAGACAGGGTTTCTC | 75763 |
rs51816053 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71097940 | GACATCCCGTTTTCC[A/C]ATTTGTTAAAGATGC | 75763 |
rs51906811 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71089249 | GCAGGTGTGTCAGCC[C/T]AACTTAGAAGTGAAG | 75763 |
rs51932144 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112446 | ATGAACTGTTGGAGT[G/T]CGTGAAGGGGCCAGT | 75763 |
rs51963577 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060850 | GTGAGATTTCCCCAT[C/T]CACGTGCAGATGTCA | 75763 |
rs52016372 | snp | C/T | | | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71088690 | AGAGTACCTACCAGC[C/T]GGGCGTGGTGGCGCA | 75763 |
rs52084985 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71089381 | TCTGGCCTGTCTACA[A/G]CACACATGCACACAC | 75763 |
rs52089432 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71064146 | TGCTTGCTTGCTTGC[G/T]TGCTTGCGTGCGTGC | 75763 |
rs52099434 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71064103 | AAGCGTGTAGGGGGC[A/G]TTTTGTTTGTGTGCT | 75763 |
rs52102177 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105387 | GCCAACCATGACCTG[C/T]CCCAATGTAGCCCAC | 75763 |
rs52132425 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71085545 | TCTTCTTTCCTTTCC[C/T]TTCCCTTCCCCTTCC | 75763 |
rs52143789 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71064162 | TGCTTGCGTGCGTGC[G/T]TGCTTGCTTGCTTGC | 75763 |
rs52194129 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71064021 | CCCTGTCTCAAAAAA[A/C]CAAAATAAGTGAAGA | 75763 |
rs52226615 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105412 | GCCCACTGCCCCTCC[C/T]CCCTCCATCCCTCCC | 75763 |
rs52234049 | snp | A/C | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71060292 | AAACAACTACTACta[A/C]taataatgataataa | 75763 |
rs52410159 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71064130 | TGCTTGCTTGCTTGC[G/T]TGCTTGCTTGCTTGC | 75763 |
rs52415181 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71064142 | TGCTTGCTTGCTTGC[G/T]TGCTTGCTTGCGTGC | 75763 |
rs52442441 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71064154 | TGCTTGCTTGCTTGC[G/T]TGCGTGCTTGCTTGC | 75763 |
rs52506447 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060290 | TAAAACAACTACTAC[A/T]aataataatgataat | 75763 |
rs52521145 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105393 | CATGACCTGTCCCAA[G/T]GTAGCCCACTGCCCC | 75763 |
rs52575286 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71089349 | AGAGGAACTGAGGAA[A/G]ACATCTAACATCACT | 75763 |
rs107618429 | snp | C/G | | | utr-variant-3-prime, intron-variant | Dcaf17 | Mm_Celera | 2:71099093 | ACTGAGTTTCAGGCA[C/G]ACACCACCATACCAT | 75763 |
rs107663200 | snp | A/G | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71071524 | GGGGCAGAGGCAGGT[A/G]GATTTCTGAGTTCGA | 75763 |
rs107689611 | snp | C/T | | | utr-variant-3-prime, intron-variant | Dcaf17 | Mm_Celera | 2:71099079 | TCAGCGTCTCAAGTA[C/T]TGAGTTTCAGGCACA | 75763 |
rs107773857 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105433 | CATCCCTCCCTCCTT[A/G]TCTCCCCCGACTCAC | 75763 |
rs107981302 | snp | C/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105759 | TCCGTTAGCGTCCTA[C/G]CAGTGTCTTCCTCCA | 75763 |
rs108106287 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105753 | TGCTCTTCCGTTAGC[A/G]TCCTAGCAGTGTCTT | 75763 |
rs108121406 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111175 | TGAGGCTCTGGCCAG[A/G]CCCTGAGTGCCGACT | 75763 |
rs108130923 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060326 | tgaataatattaata[A/C]taGTGCTTTTTTTCT | 75763 |
rs108164010 | snp | A/T | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71071430 | TTTGTCTCAAAAAAA[A/T]TTTTTTTTACCAAAA | 75763 |
rs108374997 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111716 | CTCAACCATCTGTGT[A/G]ACAGGGACTCCTTCA | 75763 |
rs108398586 | snp | C/G/T | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71071523 | GGGGGCAGAGGCAGG[C/G/T]AGATTTCTGAGTTCG | 75763 |
rs108610989 | snp | C/T | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71071537 | GTAGATTTCTGAGTT[C/T]GAGGCCAGCCTGGTC | 75763 |
rs108810697 | snp | A/T | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71071428 | ATTTTGTCTCAAAAA[A/T]ATTTTTTTTTACCAA | 75763 |
rs108856114 | snp | C/T | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71071266 | CCTTCTCCAAACCAG[C/T]TTTTAACTGGTATGA | 75763 |
rs211852498 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105784 | CCTCCAGATGCTGCT[C/T]GGCCCTGACTGCTGT | 75763 |
rs211858485 | in-del | -/A | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71089961 | ACTTGAGACTTGGTT[-/A]AAAAAAACGAGCCTC | 75763 |
rs211903996 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71087772 | TGCTTCCCAAGTGCT[A/G]GATTAAAGGGGTGCA | 75763 |
rs211906485 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077982 | ATAGATTTAAAGCAT[A/G]AAATACAGGCATTCT | 75763 |
rs211940270 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71078629 | AAAGTAAGTGCTCAT[A/G]TAAATAGTCATGCGC | 75763 |
rs211971965 | in-del | -/GTGGCACACAACTTTA | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091930 | CCAGGCCAGTAAGTG[-/GTGGCACACAACTTTA]GTCCCAGCATTTAGT | 75763 |
rs211985775 | in-del | -/AA | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111112 | AGGAGGTATTAAAAA[-/AA]GGGGGGGGGGTCAAA | 75763 |
rs211998945 | snp | C/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71058762 | GAGGTGGGGTAGGGG[C/G]CTGTAGCGTCAGCCC | 75763 |
rs212002119 | in-del | -/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091767 | CCAGCCTGGACTGCA[-/T]TGAGACTCTGCTTAA | 75763 |
rs212009163 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062968 | GAGAGCTGAGCATGC[A/G]CACCTTCAGTCTCAG | 75763 |
rs212030504 | in-del | -/A | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112898 | ACTAGCGCCCATAGG[-/A]AAAAAAAAGGCCAAA | 75763 |
rs212114326 | in-del | -/AGT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71103472 | TTCTTGGACCCACTA[-/AGT]AGTCCCTCACTGCCT | 75763 |
rs212234815 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71086333 | TGTAAGCACCTCGAC[A/T]CATAGCTGCACTTTC | 75763 |
rs212240586 | snp | C/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71064081 | GTGTTTGTGTGTTTG[C/G]ACATGCAAGCGTGTA | 75763 |
rs212439755 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71097629 | CGTCTGCCAGGTGTA[C/T]GGTTGGCAGAGATTG | 75763 |
rs212460369 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71113063 | GTCTCAAAAAATAAA[A/G]GTCAAACATGCTGGC | 75763 |
rs212487854 | in-del | -/AC | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71094546 | GTCTTCCCCCCCTCT[-/AC]CCCCCCCTGAAATCT | 75763 |
rs212579420 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71092441 | GCTTTTATGCAGTAT[C/T]TTAACTGTACCTGTC | 75763 |
rs212587117 | in-del | -/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71080299 | CCAGAATAAACAGGA[-/T]TTTTTTCTATCATCA | 75763 |
rs212599152 | in-del | -/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71102611 | AAATAAAAATAAATC[-/T]TTTTTTAAAAAATTG | 75763 |
rs212620697 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71103159 | ATTGTCCTCTTTACT[C/T]TTCCCCGTCCTTGGG | 75763 |
rs212770841 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71109388 | CCTACCTTGTTAAGA[C/T]TCATGATACCTCCTC | 75763 |
rs212818984 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71100208 | CTACTCTAACTTTTA[A/G]AAAAATTAAATTGGT | 75763 |
rs212858349 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110078 | CAGTGTCAAAAAGCT[A/T]GTTGATACATGAAAT | 75763 |
rs212908077 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71071830 | CTGTCTTCACAGCAG[C/T]ATGGAAAGAACTGAA | 75763 |
rs212910923 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71079957 | AGCCACCATGTTGTT[A/G]CTCAGATTTGAACTC | 75763 |
rs212998062 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71057129 | GATTATGGAATTGCC[A/G]CTCTTTATCTTTCAC | 75763 |
rs213043968 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71072945 | ACTGGAGATACTCAG[A/C]AATAGAACAGCAAGT | 75763 |
rs213063437 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098408 | ATTAGATTGTAACAT[A/C]CAAAGCTACATTTGA | 75763 |
rs213120250 | snp | A/G | | | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71106380 | CAACAGAGGTAGTGG[A/G]AAAGAAAGGTTACTA | 75763 |
rs213201454 | snp | C/T | | | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71088702 | AGCCGGGCGTGGTGG[C/T]GCACGCCTTTAATCC | 75763 |
rs213226464 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71089379 | TCTCTGGCCTGTCTA[C/T]AACACACATGCACAC | 75763 |
rs213387659 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71100009 | AAATTTATTTTAAAG[C/T]CTCCTCTAAACAAAC | 75763 |
rs213422556 | snp | A/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090536 | GTAGGATTTGTAATG[A/T]AAAATCATACTTTTG | 75763 |
rs213747607 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71106963 | CCCTTCATCACTCGT[C/T]CTTTCACGTGTCTGC | 75763 |
rs213767432 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71109310 | GTGGAGCCAGTCTGA[G/T]ATGGAGAGGAGTCTC | 75763 |
rs213803350 | in-del | -/TG | | | intron-variant | Dcaf17 | Mm_Celera | 2:71102073 | ACTACATACAGGGAC[-/TG]TGTTCCAAACAAAAC | 75763 |
rs213859472 | in-del | -/A | | | intron-variant | Dcaf17 | Mm_Celera | 2:71075594 | ACTCCCTTTTTTTTT[-/A]AATGCAGAATCTCAC | 75763 |
rs214038372 | in-del | -/GAC | | | intron-variant | Dcaf17 | Mm_Celera | 2:71103412 | AGGCTCTGAGGTATA[-/GAC]GGCTCATACAGGGAG | 75763 |
rs214092411 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105092 | TCACTGATTCTTGTT[G/T]GAAGGAGGCCTCTGT | 75763 |
rs214353178 | snp | G/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71094011 | CAGCTGCTCACTCCG[G/T]AGAGTTGCTTCTCAG | 75763 |
rs214371237 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098961 | TTAGTTTGGGGGTTG[G/T]Gtttttttttttttt | 75763 |
rs214404229 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71079825 | GTTACTTCTTATGAT[A/G]CTGAGAACATTTTCA | 75763 |
rs214449311 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71071692 | CCCCCCATGGTCTTA[C/T]CTATTCTCTTGATGT | 75763 |
rs214489969 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077338 | GATTCCTAGTCCATG[A/G]GTAACTGCAACCCTA | 75763 |
rs214575337 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105747 | GCTGCCTGCTCTTCC[A/G]TTAGCGTCCTAGCAG | 75763 |
rs214645735 | snp | C/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091222 | ATAAAGGGGCCTCTG[C/G]TAGGCCCCTTCTGTG | 75763 |
rs214669863 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71102479 | TTAAGAGCACTGACT[A/G]TTCTTCCAGAGATCC | 75763 |
rs214757024 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71076197 | ATTATGTTCCCACTT[A/T]TCTCAATTTGTGGAG | 75763 |
rs214798784 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059066 | TGTATCCACAAGTGC[G/T]CAGTCAAAATAATAT | 75763 |
rs214830441 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71092703 | ACAAGATAGTAACGT[A/G]TTAAAGTCTAATACT | 75763 |
rs214855691 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060556 | GAATTCTATACATGA[A/G]TACTGTATTTACATA | 75763 |
rs214870649 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059576 | TTTTAAATGCTAAGG[A/G]CCAGAGACATGGCTC | 75763 |
rs215014628 | in-del | -/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71061387 | GAGATCATCCCACCC[-/T]TGTACTAAGACAAAT | 75763 |
rs215071240 | in-del | -/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105409 | TAGCCCACTGCCCCT[-/C]CCCCCCTCCATCCCT | 75763 |
rs215202774 | in-del | -/GCATGCCT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077012 | GTGCTATGAAAAAAG[-/GCATGCCT]GCCTTACTTTTTATT | 75763 |
rs215204281 | in-del | -/CT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71101174 | GACCCATGGATGAGA[-/CT]CTGTTAGAAAGATGC | 75763 |
rs215277550 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71073808 | TGACTGTCAGATAAT[G/T]TACTTAGAATTCTTG | 75763 |
rs215310304 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059015 | ATATTTAATATTTAT[A/G]AAAGGAATAAAGTAG | 75763 |
rs215426650 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71099943 | GCAATCCTAACACTG[A/G]GTCATGAGTTCTAAA | 75763 |
rs215440017 | in-del | -/TCCACACC | | | intron-variant | Dcaf17 | Mm_Celera | 2:71097778 | TTCAGAAAGTCCTTT[-/TCCACACC]TCCACACCCATGTCA | 75763 |
rs215450625 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71076085 | CAAGGTACAGCTCTC[A/T]GACTTGCAGGTACGG | 75763 |
rs215546022 | in-del | -/AAT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71076441 | TTTTACCAACTAAAG[-/AAT]AATAATAATAGCATT | 75763 |
rs215618359 | snp | A/G | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71053844 | GTTGTGGGAGAGGCA[A/G]AGATGGTCTAATGAC | 75763 |
rs215623368 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062917 | GGTGCAAGCCAGACA[A/G]CCTGAGTTTGAGCCT | 75763 |
rs215637681 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110597 | GGAAGGACCACCATG[A/G]TTTAGTTATAGTAAA | 75763 |
rs215653360 | snp | G/T | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054313 | TATGTTAAAGTGAAT[G/T]CGCGGAAGGTATGAT | 75763 |
rs215764296 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71103303 | ATTAAATCTATTCTG[C/T]CTAGAAGAGTGGAGA | 75763 |
rs215778573 | snp | C/T | | | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71082936 | GCTGAGTTAATATAG[C/T]TTATTCTGAAATCTC | 75763 |
rs215892957 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71074897 | ATGGGTCTGACAACT[G/T]TTCCATCCCTAAATT | 75763 |
rs215919055 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71061899 | TAACCCAGAAGTACT[A/G]TTTAAGCCATGAGCA | 75763 |
rs215945766 | in-del | -/TTG | | | intron-variant | Dcaf17 | Mm_Celera | 2:71081630 | CAGCCTCCTTTATTA[-/TTG]TTGTTGTTGTTGTCT | 75763 |
rs215964138 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110104 | GAAATGAGATGTCAC[G/T]TTATGTCCTACAGGG | 75763 |
rs215996179 | in-del | -/CCC | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71071670 | CTATAAGAATTAAAT[-/CCC]CCCCCCCCCCATGGT | 75763 |
rs216203384 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060490 | AAGCTTCCCCCATAC[C/T]TAAATGTTTGTTCAT | 75763 |
rs216211103 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71081493 | TTAGGCCTGATTAGC[C/T]GCTACAATTGTTCAA | 75763 |
rs216240629 | snp | A/G | | | downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71114771 | GCTCACGTGTCACTT[A/G]CACACCTGCAGGTCA | 75763 |
rs216354334 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077379 | GGAGAGCTTATCTTC[G/T]GGCTTGCTGGACAGC | 75763 |
rs216388615 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077822 | ACAAAGTTGTACAGT[A/G]CACATGTGCTGACAC | 75763 |
rs216390596 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71061212 | TCAGGTATAGCTGAG[C/T]GTGAGCTTGAACCTT | 75763 |
rs216449276 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110237 | GTAAGGGCTGCTCTG[C/T]ATCTCTCCATAGGTC | 75763 |
rs216466279 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71061846 | AACGTCTGAAAGTCT[A/G]GTTGGTTGCTCTTCA | 75763 |
rs216635013 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71080727 | GAGTTTATTATTACA[C/T]GGTGTTTGAATTTCT | 75763 |
rs216647958 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077881 | CTATTGATGCTCCAG[C/T]CCGAGGCTTGCTGCT | 75763 |
rs216683956 | in-del | -/TTATA | | | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71082955 | TTCTGAAATCTCTTG[-/TTATA]TTAGATAAATTTACT | 75763 |
rs216701736 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110823 | GCATCTGTAAGCGAG[A/G]CCGTGACCTAAGCTG | 75763 |
rs216724744 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112262 | GGAACCTCAAGGACT[G/T]AGGCTTGTATATAAA | 75763 |
rs216746633 | in-del | -/GAGTG | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71061593 | GACCCGAGAAGCTAG[-/GAGTG]ACTTGGTCTGGGGAA | 75763 |
rs216762168 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111478 | CACTATATAGATTTT[G/T]TTTTGTTTTGTTTTT | 75763 |
rs216845799 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71102618 | AAATAAATCTTTTTT[A/T]AAAAATTGACCCTTG | 75763 |
rs216889415 | in-del | -/A | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110632 | CGACAATCTTTTGTG[-/A]GACAGCTTATCTATT | 75763 |
rs216891390 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71074100 | TCTCTTTAAACATCA[C/T]TAAACAACTTTTAAG | 75763 |
rs216905597 | in-del | -/GGTTT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098961 | TTAGTTTGGGGGTTG[-/GGTTT]TTTTTTTTTTTAATT | 75763 |
rs216925014 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71074812 | TGTGTTTTAACTTTT[A/G]CTTCCTGTGGTTTTG | 75763 |
rs216984570 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71085216 | GACTGATGGGCTAGC[A/G]TTTGTTTGCTGTTGG | 75763 |
rs217061185 | snp | C/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105976 | ACCACAGTTTTCAGC[C/G]ACTCCCCAACGCGTT | 75763 |
rs217209064 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71079315 | TTGTCCACATAATGA[A/G]TTTGAGGCCAGCCTG | 75763 |
rs217313973 | in-del | -/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105341 | TGGGAATGCCAACAA[-/G]GGAAGAGCCCTTTCA | 75763 |
rs217379988 | snp | A/C | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71064789 | GTAACAAGTGCTCTT[A/C]ACCACTGAGCCATCT | 75763 |
rs217428096 | in-del | -/GTGTGTGTGTGTGTGTGTGTGT | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | GRCm38.p3 | 2:71092931 | AGTTTGTTTTCTGGG[-/GTGTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 75763 |
rs217435256 | snp | C/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71078812 | ATATATACACACACA[C/G]ACACATAAAAATTAT | 75763 |
rs217459944 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71063159 | ATAAAATGTAAACGC[A/G]TTAAAACATAAAGAC | 75763 |
rs217474336 | in-del | -/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090893 | CTGATACTGCTAGCC[-/T]GGTTGGCTGGTCAGG | 75763 |
rs217522609 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110394 | GGATATAACAAGGCC[A/G]ATTGCTCTCAATAAA | 75763 |
rs217538862 | in-del | -/TTTA | | | downstream-variant-500B, intron-variant | Dcaf17 | Mm_Celera | 2:71095906 | GTATATATATTTGTC[-/TTTA]TTTATCTTGGATAGT | 75763 |
rs217627296 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71093366 | GACATTTCTTAGATA[C/T]GTGGTAAGAAAAAGG | 75763 |
rs217730739 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71114204 | CCACCCCTCCCAGTG[C/T]AAACTCATTCCTGGA | 75763 |
rs217827892 | in-del | -/AAAAAC | | | cds-indel, intron-variant | Dcaf17 | Mm_Celera | 2:71090608 | AAAAGAAAAAAAAAA[-/AAAAAC]ATATCAATTCTAGTT | 75763 |
rs217901956 | snp | A/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71095184 | CTATCAACAAAAGAT[A/T]ACAATGATGATAGTG | 75763 |
rs217909358 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112734 | TACAGAGGCATGATC[A/G]GGTTTGGGGTGCATG | 75763 |
rs217935082 | in-del | -/TGAT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71075746 | CTTAATTGCAATATC[-/TGAT]TGACAATTAGAAATA | 75763 |
rs217944421 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71113458 | TTGAAGAGGAGAAGA[A/G]TCAGCTCTGATATTT | 75763 |
rs218092104 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077663 | CAAGATACAGTATAA[A/T]ATTTTGTCCTTGTGA | 75763 |
rs218096120 | in-del | -/AA | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060177 | CAAATTTGTGATTAG[-/AA]AAAAAAAAAGACAGA | 75763 |
rs218272857 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71056616 | AATTCTTGGTGATGA[-/T]TTTTTTTTTTTTTTT | 75763 |
rs218305586 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71094760 | AGAACAGTGAGGACC[C/T]GGGAGCTGTTATTGA | 75763 |
rs218345393 | in-del | -/GTTTGTTTGTTT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71079036 | TCCTTATAGCTTAGG[-/GTTTGTTTGTTT]GTTTGTTTGTTTGTT | 75763 |
rs218416622 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71081127 | TCTGTCTACAGACAC[A/G]AAAGACATGGCAACC | 75763 |
rs218417089 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71072071 | TATACCCTCCCCCCG[C/T]CCTGCTCCCCTACCC | 75763 |
rs218513729 | in-del | -/TTTC | | | intron-variant | Dcaf17 | Mm_Celera | 2:71086820 | AATTTATCTCACTTA[-/TTTC]TTTTTTTTTCTTTTC | 75763 |
rs218560439 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059636 | TGTTGTTGCCTACAG[C/T]CTAATCTTATAGACT | 75763 |
rs218676632 | in-del | -/CATGACCA | | | intron-variant | Dcaf17 | Mm_Celera | 2:71074332 | CAGTCATCTCAACAG[-/CATGACCA]CATGCCTTTATTGGG | 75763 |
rs218682507 | snp | C/T | | | downstream-variant-500B, intron-variant | Dcaf17 | Mm_Celera | 2:71099333 | GGTACATTCTCCTGA[C/T]TGATGATTGATGTGG | 75763 |
rs218898795 | in-del | -/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111240 | CAATGGAGAAGTAGA[-/T]TTTTTTTCTTCCATT | 75763 |
rs219057425 | snp | A/G | | | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71088942 | TATTTCCTTACCATA[A/G]TCTTTTATTTTGCTC | 75763 |
rs219072205 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71088106 | GCCTGTAACGCCAAC[C/T]CCAAGGGATCCAGTG | 75763 |
rs219128702 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71089680 | TTTCTGACAAGTCTT[A/C]TGCATCGGTGTGCAT | 75763 |
rs219146464 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71078976 | CTGGTCCTTGATTTT[G/T]TTGTCTGGAAAATGC | 75763 |
rs219149825 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Dcaf17, Mettl8 | Mm_Celera | 2:71055557 | TCCAGGTTTACCGCG[C/T]GCAGCCCGGAAGGCT | 75763 |
rs219228352 | in-del | -/CGCACACACACACA | | | intron-variant | Dcaf17 | Mm_Celera | 2:71061009 | CCCCATGTGTGTGCG[-/CGCACACACACACA]CACACACACACACAC | 75763 |
rs219252259 | snp | C/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71097816 | TGTTGGGTACTGCCT[C/G]TGTTTCTTCCAGCAG | 75763 |
rs219310367 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71087896 | GTGAGTAATAAATAT[A/T]GCTGAACGGTAGAGT | 75763 |
rs219367373 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098665 | TGGAGATAGCCTGTC[G/T]TTGCCATGTATCCGG | 75763 |
rs219492319 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71056387 | AAAAAAAAAAAAAAA[A/G]GGAGAAACAATGTAC | 75763 |
rs219518201 | snp | A/C | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054796 | AAATGAAACGGCTAA[A/C]GTTTGATCCAGCACA | 75763 |
rs219556365 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71096962 | CTCCCTTCCTGTGGC[A/G]ACTAACTTCAGTCAG | 75763 |
rs219764769 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71097059 | TGAAATTTTCATGAT[A/G]TCACCTTGTTCTTTA | 75763 |
rs219820899 | in-del | -/AT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71102421 | ACTGACTTTAGTTCA[-/AT]ATAAAAATATTGACC | 75763 |
rs219837845 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098024 | AAGTTCTGAGTAGTC[A/G]TGTTTGGGTCTTTGA | 75763 |
rs219842754 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71086774 | CGTACTCCCACTTAC[A/G]TGTGAGATTTGAAGA | 75763 |
rs219875536 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71087990 | AGCTAAACAGAAAAC[A/G]GGAGAGGTGGCTTGC | 75763 |
rs219916514 | in-del | -/TCTA | | | intron-variant | Dcaf17 | Mm_Celera | 2:71108326 | CTCTCTCTCTCTCTC[-/TCTA]TCTCTTTGTCTTTTT | 75763 |
rs219946644 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062140 | TCATTTTCTTGAGGG[A/G]AGATTAGAGAGATGA | 75763 |
rs219995899 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71057579 | GTGCTGGTGAATCTA[-/C]CCATGTCCCTCGATT | 75763 |
rs220081073 | snp | A/C | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71053968 | TGTGCAGTCCCTCAG[A/C]CAGCTCACTGGCTGT | 75763 |
rs220115508 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091599 | TGTAATCCAGCACTC[A/G]GGGAGCTGCAGCAGG | 75763 |
rs220144618 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71095743 | TCACTCGTTCATTAC[A/G]TTTTATTCCTGAATC | 75763 |
rs220201398 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71081893 | AAGCTAATAAATTTC[C/T]CTTGCTCATCCCTAC | 75763 |
rs220237672 | snp | A/T | | | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71083115 | GGGGTCCTGTTCCCG[A/T]CTTCTACTGATGTCA | 75763 |
rs220322609 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062976 | GCATGCACACCTTCA[-/C]GTCTCAGCACTAGGC | 75763 |
rs220433960 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71073366 | GCTCTAGTGCTAAGC[C/T]TCACCCTCAGCTGTT | 75763 |
rs220461720 | snp | A/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090910 | GTTGGCTGGTCAGGG[A/T]TGCTGCTGTCTCTTT | 75763 |
rs220543035 | snp | C/G | | | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71057591 | CTACCCATGTCCCTC[C/G]ATTCGCCCTTGGATG | 75763 |
rs220549639 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059383 | CTACAGGCTTTCCTA[C/T]AGCCTGATCTTTTTT | 75763 |
rs220582603 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059660 | ATAGACTTTTTCTTA[C/T]TTGAGGTTCGCTCTT | 75763 |
rs220634161 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71058220 | GCTTCTCCCTATGCT[C/T]TTACGAAAACAGCCA | 75763 |
rs220868659 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71100432 | CCTTCAATTTCTCTG[A/G]CTGAGACTGACAATG | 75763 |
rs220954508 | snp | A/G | | | downstream-variant-500B, intron-variant | Dcaf17 | Mm_Celera | 2:71099622 | TGAGCAAATTGACTG[A/G]CTCTCCTTACTGAAA | 75763 |
rs221002060 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71061487 | AATAGTATAAAAGTT[-/A]AAGCTACATAGTGAA | 75763 |
rs221164674 | in-del | -/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71095816 | GGGTTGTTTCTGCTA[-/T]TTTTTTTTCTTACTG | 75763 |
rs221178702 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71109572 | TTATACTTTGAATAT[A/G]CTCGTGTTGAAGGTC | 75763 |
rs221178936 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71099661 | AATGCTGCTTCAGAT[A/T]CCACTGAATCCAGGC | 75763 |
rs221272897 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098843 | TTGCTTTTGGGTTTA[A/G]TACAAGTATCTAGGC | 75763 |
rs221289113 | in-del | -/C | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71109782 | CTCACGCCTCTCCCT[-/C]TCCCCTCCCCCTCCC | 75763 |
rs221345578 | in-del | -/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111113 | AGGAGGTATTAAAAA[-/G]GGGGGGGGGTCAAAA | 75763 |
rs221418493 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71057358 | TGGGGATCTAAATTC[C/T]GGTCCTCATGCTTGC | 75763 |
rs221457661 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71102772 | GGCTCGGGGGAAGCA[A/G]CTTGCTCCCGAAACA | 75763 |
rs221458679 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71093567 | CAGCCACTTTTAAAC[A/C]CAGCTCCATCCAAGA | 75763 |
rs221519011 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71094701 | TGCCATTGTCTTTCC[C/T]CTTGTACACCCGGGG | 75763 |
rs221599242 | snp | C/T | | | downstream-variant-500B, intron-variant | Dcaf17 | Mm_Celera | 2:71096045 | TTTGCAGTTGTTCTT[C/T]ATTTTTTTAACGTTT | 75763 |
rs221704416 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060719 | TTACTGTGCTCATGT[A/G]CATATGTGTTTAGGG | 75763 |
rs221802223 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71080073 | TTCTATCTGCATGTA[C/T]ACCTGCATGCCAGAA | 75763 |
rs221814830 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71064679 | ATGTATGCCCAGTGG[-/C]CATGGAGGTCAGAAG | 75763 |
rs221815344 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71061369 | TAGTCGTTCTTCCTG[C/T]TCGAGATCATCCCAC | 75763 |
rs221893435 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104318 | GTCAGATACTGAGAG[A/G]TGCCCCTCAGCCTTT | 75763 |
rs221982881 | in-del | -/AAAAAA | | | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71056704 | TGAAATTGGAAGATG[-/AAAAAA]AAAAAAAAAATGAGT | 75763 |
rs221992746 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71106090 | CCAGATGTCCCTGAC[G/T]AGAGTCAGCATCAGC | 75763 |
rs222049615 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71102055 | AGTTCAAGGTAATAA[G/T]GGACTACATACAGGG | 75763 |
rs222090815 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71063669 | TGCTCTAGTTGAAGA[C/T]TTGAGGCTCATGACC | 75763 |
rs222217542 | snp | C/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71063439 | GCTGCTTCGTATATC[C/T]GCAACTACAGGGGAA | 75763 |
rs222219971 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71109859 | CTCCCAGATGAGCAG[C/T]TTTGAGCAGCTTTGC | 75763 |
rs222293704 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71079628 | GATGCTTGTGTGTCT[G/T]TTGCGCTCTGTGGAG | 75763 |
rs222294413 | in-del | -/A | | | intron-variant | Dcaf17 | Mm_Celera | 2:71103844 | ATGGGGAACTGTATT[-/A]AAGGGTCGTAGCATT | 75763 |
rs222298778 | in-del | -/A | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71092287 | AAGATGCTTAGCACG[-/A]AAAGTGTTTTGTAAG | 75763 |
rs222302180 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060649 | CGAGTTCTTGGCTTC[A/G]TCTTGATTATGGGAC | 75763 |
rs222303978 | in-del | -/ACAGACAGACAG | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71061050 | CACACGCACACAAAC[-/ACAGACAGACAG]ACAGACAGACAGACA | 75763 |
rs222336868 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098059 | GTTCCACTCATCTAC[A/G]TTTCTGGTTTTGTAC | 75763 |
rs222379038 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111891 | GCATTGTTTCAGTAG[G/T]AAGATCTAATTATAA | 75763 |
rs222407651 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71085952 | TTGTACTTTTGAAGT[A/G]TTTTAATGATGTGAA | 75763 |
rs222469983 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71103017 | CCATCTTCCTCCCAG[A/G]TGGTGCCTCTGATCA | 75763 |
rs222547026 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71075402 | GAAGGTAGTGTTTTC[A/G]GAAGTGCTTTGGAGA | 75763 |
rs222589059 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104657 | CAACTATGAGTAGGC[A/T]TCAAGTGGGGAGAGG | 75763 |
rs222699517 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059427 | TTTTTTTGGTTTTTC[A/G]AGACAGGGTTTCTCT | 75763 |
rs222777014 | snp | G/T | | | missense, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71078150 | CTCTACAGCTTCCAA[G/T]CCATCATCGAACAGG | 75763 |
rs222869683 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062249 | AACCTACTCTTATTC[C/T]ATAAACACTTAAGTG | 75763 |
rs222874237 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110970 | GATATGTACTAAGGG[A/G]TGCATACCCAGTCAC | 75763 |
rs222949134 | in-del | -/A | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71093259 | GCAAAGAGTCTTTCT[-/A]AAGGTAGGAATTGAA | 75763 |
rs222989370 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71075104 | TTTGTTGGTGACATA[A/G]CCATAGTAACCATAG | 75763 |
rs223024109 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059715 | TTGATATAAAACTAG[C/T]TGACACATTACAGGA | 75763 |
rs223034052 | in-del | -/TTTT | | | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71056958 | TTGTTTTAGAAGTAC[-/TTTT]TTTTTTTTTTTTCCC | 75763 |
rs223084927 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71074367 | GGGTTCTCTTGGGCC[A/G]TGTTTCACACTGTTA | 75763 |
rs223162008 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71113409 | AAAGGAGCCAAGATT[A/G]ATGGCCTGAGTTCAA | 75763 |
rs223214886 | snp | A/G | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71109715 | TGGAAAGAAGTAGGC[A/G]GGACTAAGTTGAAGG | 75763 |
rs223258310 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71100512 | CTGCACACGAGAGAG[A/G]ACTTAAGGAAGAGAA | 75763 |
rs223409998 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71072055 | TATCCCGAAAGTTCC[C/T]TATACCCTCCCCCCG | 75763 |
rs223474557 | in-del | -/CACACACA | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077575 | CACATAGCTCGCATG[-/CACACACA]CACACACACACACAC | 75763 |
rs223705049 | in-del | -/TTT | | | intron-variant, utr-variant-3-prime | Dcaf17 | GRCm38.p3 | 2:71082782 | GAGGTTTTTAATTGA[-/TTT]TTTTTTTCCCTTTTA | 75763 |
rs223757823 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71093654 | TTCACACACATACAT[A/G]CAAATATACACAACA | 75763 |
rs223769325 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71073108 | GTTAAATTCCTCTCC[A/G]TTCCTTCAAAAGGTA | 75763 |
rs223884304 | in-del | -/A | | | intron-variant | Dcaf17 | Mm_Celera | 2:71073509 | AGACCCTGTTTAATT[-/A]AAAAAAACATGACCG | 75763 |
rs223907547 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71084751 | TCCTTGACAGATGAT[A/C]CGTGAATGAATGAAA | 75763 |
rs223933955 | snp | A/T | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71071620 | AAAAAAAAAAAAAAA[A/T]TTTTTTTTTCATTAG | 75763 |
rs224040455 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090023 | TGGAACATTCTGCAG[C/T]ATTTTCCAGAACAAG | 75763 |
rs224105635 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090733 | ACATATTTGCATGTT[C/T]ATGTGTATGTGGGTG | 75763 |
rs224117671 | snp | A/T | | | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71106430 | CCTGTTTAGAAATTG[A/T]TCTTTGGAGCAAATC | 75763 |
rs224151240 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71081326 | TGGTGTCTACTCTCT[A/G]CTAAGGTCTCCATTG | 75763 |
rs224160831 | in-del | -/TCCCCATCTCCC | | | intron-variant | Dcaf17 | Mm_Celera | 2:71113477 | GCTCTGATATTTCTG[-/TCCCCATCTCCC]TCCCTCTCTCCCTCC | 75763 |
rs224218994 | snp | C/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110144 | GGTAGCCTTGACCCA[C/G]CTGCCTTGAGAGGCA | 75763 |
rs224270614 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71079255 | CATCCCTAAATGCCA[A/G]CTCCTGAGAGGTAGA | 75763 |
rs224356550 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71079726 | CATCCAATGACAATT[C/T]GATGACTGCAGTGTG | 75763 |
rs224404097 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71064124 | TTTGTGtgcttgctt[A/G]cttgcttgcttgctt | 75763 |
rs224654378 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112664 | TTTTTTTAATTTTTA[A/C]TTTTAATCTCTCTTT | 75763 |
rs224690088 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71103782 | CTCATAACAGTAGAC[A/G]CAGTTATACAGTAGC | 75763 |
rs224826793 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71076483 | TTTATTTTATACTAG[A/G]TACTTTTAAGTATTT | 75763 |
rs224921830 | in-del | -/A | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | GRCm38.p3 | 2:71095486 | TTTTCAGTGCATTTC[-/A]AAATAAGTCACCCAA | 75763 |
rs224934976 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104406 | TCATTTTATTTTTTT[A/T]AAAGATTTATTTATT | 75763 |
rs224956545 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71085441 | CGTTCTCACCCCCAG[C/T]TTGTATACTAGCCCA | 75763 |
rs225046438 | snp | G/T | | | downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71114875 | TAGGGTCGAAGTTCT[G/T]TCAGGTCAGTATTTT | 75763 |
rs225054559 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077504 | GTGTCCTCCTCTTAT[C/T]CCTCACACATAGGCA | 75763 |
rs225183991 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098102 | GTTTTTATTACTATG[A/G]TTCTAGTATAACTTG | 75763 |
rs225184431 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111970 | GTCATCTGTGAAAAT[C/T]CTATGACATAAAAGT | 75763 |
rs225191503 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71078317 | TAGAAACAAAAAAAA[A/C]ACACAGTAACCTTGG | 75763 |
rs225255102 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71101957 | TCTACATGCTGGGTT[A/C]CAAGGTCTAAATGGA | 75763 |
rs225279169 | snp | A/G | | | missense, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71088392 | TTGGACTTACTTTCC[A/G]TAGTAGCTGTCACTC | 75763 |
rs225327160 | in-del | -/TTTTTTTTTTTTTTT | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71059393 | TCCTACAGCCTGATC[-/TTTTTTTTTTTTTTT]TTTTTTTTTTTGGTT | 75763 |
rs225344617 | snp | C/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71114025 | GCATTCCATCCCTTG[C/G]TGACTCCTGGCTCTC | 75763 |
rs225361654 | snp | A/G | | | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71083462 | AATCTTTAATCATAG[A/G]TATTGCATACTCTAT | 75763 |
rs225378764 | snp | A/G | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054086 | AACTGGCCTTGAAGT[A/G]CCACCCTGGTAAGAG | 75763 |
rs225411043 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71075678 | TTCAGAGATCTACCA[A/G]TTTCTGCCTCCCAAG | 75763 |
rs225467882 | in-del | -/GAA | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077241 | GAACGTAATAGTGAT[-/GAA]GAAGATCTGGAGTTG | 75763 |
rs225503821 | in-del | -/TGT | | | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71057196 | GCCAAGCTTCAGTGG[-/TGT]TGTTCCTCCGGAGCA | 75763 |
rs225638965 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060924 | TTGAGATTTCATGGG[A/T]ACGAGTCCCTGTCAC | 75763 |
rs225666965 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062062 | AAGTTAGAAGCCTGG[-/T]TTTTTTCCTCTTTAA | 75763 |
rs225858872 | in-del | -/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077027 | GCATGCCTGCCTTAC[-/T]TTTTATTGAATATTA | 75763 |
rs225898782 | in-del | -/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060122 | TGAACCATCTCTCTT[-/G]GATTTTTTTTTTAAC | 75763 |
rs225936089 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71093274 | TAAGGTAGGAATTGA[A/G]TTTCTTCTCCTTTGT | 75763 |
rs225991799 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71053845 | TTGTGGGAGAGGCAG[-/A]GATGGTCTAATGACT | 75763 |
rs226077816 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059199 | AGAAAGTCAGGACAG[A/G]AACTCACACGTGACA | 75763 |
rs226153222 | in-del | -/TTTT | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71106164 | GACTTTTTCTTGACC[-/TTTT]TTTTTTTTTTTTCAG | 75763 |
rs226179129 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71064579 | GTTTGAATGTTCTTA[G/T]GTTAAAAATGGTTTT | 75763 |
rs226187808 | in-del | -/TTTTTTTTTTT | | | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71057498 | ACTCCAGGAGGTATC[-/TTTTTTTTTTT]TTTTTTTTTTTTTTT | 75763 |
rs226297373 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dcaf17 | GRCm38.p3 | 2:71061993 | TTTTTTAACTATCAC[C/T]CCCCCCCCCCCATAA | 75763 |
rs226396955 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71081398 | TGTTCCTTCTATACA[A/G]GAAATGTAACACAGG | 75763 |
rs226412426 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71079007 | TGAGTTACACTGATT[C/T]ATACCTTCTTAACTT | 75763 |
rs226505676 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71057868 | GGGACCTTACAAAGA[A/G]AAGTGTAGTTAGGGC | 75763 |
rs226556679 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71113831 | CCTTTTTCTGTTATT[A/T]TAAAGCCCAAAGGAA | 75763 |
rs226570556 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71089703 | GTGTGCATATGTAGG[A/G]GCATAGGGTAGGTGC | 75763 |
rs226626459 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71089291 | GAGGCAAGATGACCA[A/G]ACTAGCTAAATCCCT | 75763 |
rs226633276 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71099960 | TCATGAGTTCTAAAC[C/T]AGCCTGAGCTACATG | 75763 |
rs226776177 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71071689 | CCCCCCCCCATGGTC[C/T]TATCTATTCTCTTGA | 75763 |
rs226788089 | snp | A/T | | | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71056287 | GCCTGGCGTAGTTTT[A/T]AAAAAGCTTCTTTTG | 75763 |
rs226803144 | in-del | -/CAGTGAGTTC | | | intron-variant | Dcaf17 | Mm_Celera | 2:71063978 | CCATGCTGGTCTGCA[-/CAGTGAGTTC]CAAGACAGCCAGGGC | 75763 |
rs226857611 | snp | A/G | | | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71088839 | AAAACCAAAAAAAAA[A/G]AAAGAAAGGGTACCT | 75763 |
rs226946122 | in-del | -/GG | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054673 | GGTCATGAAATATCA[-/GG]GGGGGAAAAAAAAAA | 75763 |
rs226956010 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054018 | CACTTACTATGATGA[C/T]TTAGGGGCCAAGCTT | 75763 |
rs226977988 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71061831 | TGCAGCGAATTAATC[-/A]ACGTCTGAAAGTCTA | 75763 |
rs227018497 | snp | A/C | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | GRCm38.p3 | 2:71054709 | CAACAAAACAACCAA[A/C]CAAACAAACAAAAAA | 75763 |
rs227033897 | snp | A/G | | | downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71114687 | TGATTTGTGGCTCTC[A/G]TTTATTGATCTTCTC | 75763 |
rs227086925 | snp | A/T | | | downstream-variant-500B, intron-variant | Dcaf17 | Mm_Celera | 2:71095933 | TAGTTTCTAGGAATA[A/T]GCTAGAGTTTTGCTG | 75763 |
rs227132823 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71085711 | ACAGAGATCTACGTG[C/T]CTCTGCCTCCCAAGT | 75763 |
rs227179920 | in-del | -/CAGACATGGAGT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71087464 | TTCCCCTGCCCAGGG[-/CAGACATGGAGT]CAGGCACCCTGCAGG | 75763 |
rs227240104 | in-del | -/AT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71073281 | TTGAGCAGACTACTC[-/AT]ATGGGCTTCTCTCTA | 75763 |
rs227331391 | in-del | -/ACACACACACACACACACACAC | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110012 | TGGTCCTCCTCTCCT[-/ACACACACACACACACACACAC]ACACACACACACACA | 75763 |
rs227383590 | in-del | -/A | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090811 | GGCCAGATGTCAGCC[-/A]AATGGTGTTCTCAAG | 75763 |
rs227409617 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098244 | AATTCAGTCACCTGG[A/G]GGATTCTAAGTGCTC | 75763 |
rs227411254 | snp | C/T | | | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71106303 | TGTAGGTTTAAATTT[C/T]TCTCCACCCCACCTT | 75763 |
rs227450092 | in-del | -/TGGGATGCC | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71105302 | GCTGGTAACATTTGA[-/TGGGATGCC]TGGGATGCCTCAGAA | 75763 |
rs227489018 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71064437 | CCTGCTTCCTCCCCT[-/C]AAGTTGTGGGATTTT | 75763 |
rs227608039 | snp | C/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71095142 | GCTTAGTATCACCCA[C/G]ACCAGTAAGGACTAT | 75763 |
rs227609605 | snp | C/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71063815 | AGTTTATAAGTACAT[C/G]CAAATGGATGTGAGT | 75763 |
rs227645491 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71113582 | TTTTTGAAGGGgaga[A/G]ggagagagagagaga | 75763 |
rs227668454 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71075820 | CTGTCTATGAAATGT[C/T]TCCTGATGTGTCTTA | 75763 |
rs227742357 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105700 | CAGAACAACCCAATC[A/T]GTCACGACGGGGAAG | 75763 |
rs227812087 | snp | C/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71093944 | GGAATAATAGCAGTA[C/G]CAACAACAAAGCCAA | 75763 |
rs227814316 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71103147 | CTACCCTTGATAATT[A/G]TCCTCTTTACTCTTC | 75763 |
rs227822924 | in-del | -/A | | | intron-variant | Dcaf17 | Mm_Celera | 2:71079350 | ACAACGGCCTCCCTC[-/A]AAAAAGGAAGGAAGG | 75763 |
rs227844219 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091074 | AAAGATTCCAGGCAA[A/G]TTTCAAATGAAAGCT | 75763 |
rs227846374 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71095008 | ATTGAATATAGTTCA[A/G]AAATGATAAGTTTGT | 75763 |
rs227901292 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71109832 | CTCCATCTCCATCTC[C/T]GGCTACCCACCCTCC | 75763 |
rs227974758 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059932 | GTTTGTTTTAAGTGA[C/T]TTATTATTTTTATTA | 75763 |
rs228084461 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71102379 | AAGGAGTTGGTTCTA[C/T]TGGTTCCAGTGTGGC | 75763 |
rs228237474 | in-del | -/A | | | intron-variant | Dcaf17 | Mm_Celera | 2:71078172 | TCGAACAGGTAGAGG[-/A]AAGCACAGTGGGGCA | 75763 |
rs228266670 | in-del | -/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059129 | TGATCAAATAAACTT[-/G]GGGGAGGAAAGAGGT | 75763 |
rs228316975 | in-del | -/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71078972 | CGTTCTGGTCCTTGA[-/T]TTTTTTGTCTGGAAA | 75763 |
rs228363038 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71101708 | TTCAGACATGAGTTC[A/G]AGCTAACAGAAAGTC | 75763 |
rs228365797 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111113 | AGGAGGTATTAAAAA[A/G]GGGGGGGGGTCAAAA | 75763 |
rs228386212 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71102290 | GTATAACATGCTTAT[A/G]ACTCTAGCACTCAGA | 75763 |
rs228423307 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71057742 | AGTCTTCAAGTCGAC[C/T]CCACGGAGCTGGTCA | 75763 |
rs228424296 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060795 | CTCTCTCTTAGAAGC[C/T]ATTAATTGCCTATAG | 75763 |
rs228459047 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71074466 | ATGAAAGACTCTAAC[A/T]AAGTAACACATTTCA | 75763 |
rs228612657 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71081477 | TGCCTATAAAAATTT[A/G]TTAGGCCTGATTAGC | 75763 |
rs228644135 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71073642 | AATACAGATTTTTTT[C/T]CTCATATTTTCTGTT | 75763 |
rs228749362 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71109010 | TGCATTCCACATTGA[C/T]CTCAAACTCACTAAA | 75763 |
rs228905309 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077837 | GCACATGTGCTGACA[C/T]ATCAGTTTGAGTCCT | 75763 |
rs228913791 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71097756 | TTCTTGGGCAAATGG[A/C]GTCTTATTCAGAAAG | 75763 |
rs228944012 | in-del | -/A | | | intron-variant | Dcaf17 | Mm_Celera | 2:71103359 | AACCATGGAGTTGTT[-/A]AAAGAATTGAAACCC | 75763 |
rs228970284 | in-del | -/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098514 | CTGTATGATGAACTG[-/T]GCCCTAGATGGGTCT | 75763 |
rs228981546 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71078433 | CAGACAGCAAATAAA[C/T]AGGCTCTAAAGCCAC | 75763 |
rs229012205 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062813 | TCAGAACTTTACTAA[G/T]TGAAAGTCAGCACAT | 75763 |
rs229230873 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71097325 | GATGGACATTTTTTG[A/G]GACATTATCCATTAT | 75763 |
rs229273037 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060830 | TCACCTAGGGTTGGG[A/G]CTTTGTGAGATTTCC | 75763 |
rs229374103 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062940 | TTGAGCCTCAGAACC[C/T]ACAGAAAGGCAGGAG | 75763 |
rs229391975 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112855 | GGGAGATGGCATTGT[C/T]AGCAAAACATGGAGA | 75763 |
rs229508009 | in-del | -/CTTAT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71102683 | TAGCACTAATAAAGG[-/CTTAT]CTTCTGCTTAAGACA | 75763 |
rs229516048 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71075928 | CAGGTGGTTTGTGTT[C/T]TGAGTGTTGGAAAAC | 75763 |
rs229532798 | in-del | -/TTTA | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71079055 | GTTTGTTTGTTTTTT[-/TTTA]AATTTTGTTAAATCT | 75763 |
rs229548660 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077168 | GTCTGAAGGAATGTG[G/T]TTTTTATGGTGTTGC | 75763 |
rs229695242 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077346 | GTCCATGGGTAACTG[C/T]AACCCTAGCACTGGA | 75763 |
rs229740122 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71079091 | TTTCTAAGGATAGTG[C/T]TTTCAAAGGAAATAT | 75763 |
rs229828129 | snp | C/T | | | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71083179 | TTTGTAAGAAAACTT[C/T]TCTCTCCATTTTCTC | 75763 |
rs229919995 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71078611 | GTATCTTTTCTCCTT[A/T]AGAAAGTAAGTGCTC | 75763 |
rs230023097 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112988 | GATCTCTGTGAGTTC[A/G]AAGCCAGCCTGATCT | 75763 |
rs230237000 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71081549 | AGTCTTGTACGTAGA[C/T]CCTCGGCGATGGGTG | 75763 |
rs230288053 | in-del | -/CT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105003 | GAGAAGAGTCCAAGG[-/CT]CTGTGATCTGGGAGG | 75763 |
rs230297733 | snp | C/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110220 | CTGTGTTCCCTCAGG[C/G]AGTAAGGGCTGCTCT | 75763 |
rs230379128 | in-del | -/TT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71080237 | ACCATTGAACTGAGC[-/TT]TTTTTTTTTTTTTCA | 75763 |
rs230384139 | snp | C/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71113923 | GCCCGGTTCCTTGCA[C/G]TGTTTAATGTCCCAT | 75763 |
rs230406193 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105400 | TGTCCCAATGTAGCC[C/T]ACTGCCCCTCCCCCC | 75763 |
rs230431568 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104803 | CAAAATCCCCCCCAA[A/G]CAGAAGGTTAAAAGT | 75763 |
rs230484872 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71105825 | GTAACAGTTACATAA[A/G]TCAGATCATAGAGCC | 75763 |
rs230564797 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71078631 | AGTAAGTGCTCATAT[A/T]AATAGTCATGCGCTG | 75763 |
rs230589650 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077781 | TTCTATGAAATAGAA[A/G]TAGAATCTGTAGTTA | 75763 |
rs230694476 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71101476 | CTGCTCTATAGAACT[A/G]GGGTAGTGTAGCCAT | 75763 |
rs230742528 | snp | C/T | | | downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71114619 | AAGGCAAAAGGTGAG[C/T]CATCCATTACTTAGG | 75763 |
rs230756212 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71109963 | GGAGAGACTCTGACA[A/T]GAGTCTATGTAAATG | 75763 |
rs230818172 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71073374 | GCTAAGCCTCACCCT[C/T]AGCTGTTCTCTTTAA | 75763 |
rs230819303 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71086452 | GCCACAGATCGATTC[C/T]CTTTGTTGAGCTTCG | 75763 |
rs230853215 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71058857 | ATCCAGGATACAGTT[G/T]TCACTGTTTAGGTAA | 75763 |
rs230861568 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71100716 | CCTACATGAGCAGCC[C/T]CACAGACAGGTGTGA | 75763 |
rs230963957 | in-del | -/TT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71073000 | GAGTCACAGGCCGGA[-/TT]TTTTATCCCCAAAAC | 75763 |
rs230964912 | in-del | -/TCAGTT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71097725 | TATTAAGAAGTCTTG[-/TCAGTT]GTTGGCCTTATTCTT | 75763 |
rs230975220 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71072891 | CCTTAATTATAAAAT[A/G]GCACACCAAGCATGG | 75763 |
rs230975997 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112360 | GAGAGCCAGTGGGCT[A/C]ACCAACTGATCTACC | 75763 |
rs231000496 | in-del | -/TTTCG | | | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71083811 | GAATAAGACTATTCT[-/TTTCG]TGTCTTAAATGCTAA | 75763 |
rs231022013 | in-del | -/CA | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077576 | CACATAGCTCGCATG[-/CA]CACACACACACACAC | 75763 |
rs231025811 | in-del | -/AAAAAA | | | cds-indel, intron-variant | Dcaf17 | Mm_Celera | 2:71090598 | AAAACAAACCAAAAG[-/AAAAAA]AAAAAAAAACATATC | 75763 |
rs231066713 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71057984 | CCAACAACTCATGGC[C/T]TGGGCTGGATGAAAA | 75763 |
rs231068402 | in-del | -/ACACACACACACAC | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110013 | TGGTCCTCCTCTCCT[-/ACACACACACACAC]ACACACACACACACA | 75763 |
rs231096115 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71113108 | CCAGCACTGGGGAGG[C/T]AGAAACAAGCAGAAC | 75763 |
rs231172436 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71072372 | TGGCATAGCCTCATA[C/T]GAAACAGCTATGCCA | 75763 |
rs231209095 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71081126 | GTCTGTCTACAGACA[C/T]GAAAGACATGGCAAC | 75763 |
rs231300067 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71086291 | TGTAGTGTCATTCAC[A/G]GGCTGAGCCAGCTGC | 75763 |
rs231421008 | in-del | -/ATAA | | | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71083432 | TCTATATGTTTTCTC[-/ATAA]ATAAATAAATAAATC | 75763 |
rs231453294 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71109915 | TCTGCCTCACCATAG[C/T]GCCCCCTACCCCCAG | 75763 |
rs231467304 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71094706 | TTGTCTTTCCCCTTG[C/T]ACACCCGGGGACGTG | 75763 |
rs231573189 | snp | A/C | | | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71106367 | CTAGCGCAGCACCCA[A/C]CAGAGGTAGTGGAAA | 75763 |
rs231616229 | snp | G/T | | | utr-variant-3-prime, intron-variant | Dcaf17 | Mm_Celera | 2:71099057 | TCCAACTCAGGGTGG[G/T]CCTGCCTCAGCGTCT | 75763 |
rs231618473 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060535 | ACTTACTTCATTTTT[C/T]AAAAAGAATTCTATA | 75763 |
rs231662514 | in-del | -/CTG | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71063012 | GAGGCAGGCAGACCT[-/CTG]AGTATGCGGCCAGCC | 75763 |
rs231686304 | in-del | -/T | | | intron-variant, utr-variant-3-prime | Dcaf17 | Mm_Celera | 2:71083250 | CTCGGTGAAACCCTC[-/T]TTTGTAACATTTTAC | 75763 |
rs231737325 | in-del | -/GAAAA | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111817 | GAAACCAGTCACATT[-/GAAAA]GAAGTTACTAACATA | 75763 |
rs231818658 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71109146 | CTTAAGTATCCTGAG[G/T]AGATCTCTTTATCTC | 75763 |
rs231874734 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71054249 | AGCAAGTGAGGGGCA[C/T]GGCCCTCATGTCTGA | 75763 |
rs231883459 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71114237 | TAACCTGCCCTCCTG[C/T]CTTTGATATGCCTCC | 75763 |
rs231900595 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090605 | ACCAAAAGAAAAAAA[A/G]AAAAAAACATATCAA | 75763 |
rs231928276 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71079779 | ATTCCATTATCCTAG[G/T]AATTTTGTCTCTATT | 75763 |
rs231977947 | snp | C/G | | | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71057098 | GATGCTTCCATGCCC[C/G]TCACCTGGATTAAGG | 75763 |
rs232021417 | in-del | -/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71095553 | ACATGTAATGAAATA[-/C]ACATACATTGTATAA | 75763 |
rs232062800 | in-del | -/A | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71093812 | GATGTTGAAGATAAG[-/A]AAAAAAATGAAGAAA | 75763 |
rs232119987 | in-del | -/GTGTGTGTGA | | | intron-variant | Dcaf17 | Mm_Celera | 2:71078735 | TGTGTGTGTGTGTGT[-/GTGTGTGTGA]GTATACCTTATAAAT | 75763 |
rs232139403 | in-del | -/AAGA | | | upstream-variant-2KB, intron-variant | Dcaf17, Mettl8 | Mm_Celera | 2:71053922 | TTCAGAAGGCCGGGT[-/AAGA]AAGAATGGGGACTGC | 75763 |
rs232261135 | in-del | -/TGTGTA | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71078859 | GTGTGTATGTGTGTG[-/TGTGTA]TGTGTGTGTGTGTGT | 75763 |
rs232429436 | in-del | -/GCTCCTCA | | | intron-variant | Dcaf17 | Mm_Celera | 2:71103063 | GGCCTGTGAGAATCC[-/GCTCCTCA]GCTCCTTTCATAGCT | 75763 |
rs232501380 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71074620 | TGTAAGCATTTCTGC[A/G]TTCAAGACTGTGTTC | 75763 |
rs232710815 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71064104 | AGCGTGTAGGGGGCA[G/T]TTTGTTTGTGTGCTT | 75763 |
rs232734927 | snp | C/T | | | intron-variant, downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71083714 | GCCTGCTTCTGCCTC[C/T]AAAGTGGTGGGATTA | 75763 |
rs232868958 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71106041 | GTGATCTCTCCCTCT[G/T]GCTCATGGGCTTGGC | 75763 |
rs232911279 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110608 | CATGGTTTAGTTATA[G/T]TAAAAGTGCGACAAT | 75763 |
rs232926809 | snp | A/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71093916 | TGAGGCCCTAGGTTC[A/T]GTTCCCAGTGCTGGA | 75763 |
rs233009532 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059542 | GCTGGGATTAAAGGC[A/G]TACACCACCACGCCC | 75763 |
rs233115570 | in-del | -/GC | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71061006 | CCTCCCCATGTGTGT[-/GC]GCGCACACACACACA | 75763 |
rs233132242 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71073869 | GATCCTCCTGCTTCA[A/G]CCTGCCAAATGCTGT | 75763 |
rs233147553 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090971 | ATCATGCCCAGATAC[A/G]TACATGGGTGGGCAT | 75763 |
rs233172908 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71097994 | TTGGCATCTTTGTCA[A/C]ATATTAAGTGGCTGA | 75763 |
rs233286751 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098383 | TTTCCAGCCAGTAAG[G/T]TAACCTATCATTAGA | 75763 |
rs233288534 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71087999 | GAAAACGGGAGAGGT[A/G]GCTTGCCAGCTAAGG | 75763 |
rs233388180 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059669 | TTCTTATTTGAGGTT[C/T]GCTCTTGTCTGGTCA | 75763 |
rs233579664 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71081494 | TAGGCCTGATTAGCC[A/G]CTACAATTGTTCAAG | 75763 |
rs233636747 | in-del | -/GAC | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060187 | GATTAGAAAAAAAAA[-/GAC]AGAACAGTTAAGGAA | 75763 |
rs233655064 | in-del | -/TT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71085494 | CAGAAATCTGAAATC[-/TT]TTTTTTTTCTTCCTT | 75763 |
rs233727171 | snp | C/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71092506 | GTGTTGAATTTTGTA[C/G]TCATTACATCATGTT | 75763 |
rs233775205 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71096363 | TGTCTCATTACTCAC[A/T]TGACCACCGGAGCCT | 75763 |
rs233823863 | in-del | -/TA | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71078737 | GTGTGTGTGTGTGTG[-/TA]TACCTTATAAATACA | 75763 |
rs233853320 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71106921 | ACATGTAAGATGAAC[C/T]AATACGTGCATGTTG | 75763 |
rs233885319 | in-del | -/AT | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090614 | AAAAAAAAAAAAAAC[-/AT]ATCAATTCTAGTTTT | 75763 |
rs233946872 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71061085 | ACAGACAGACACATG[C/T]ACACATACAGATACA | 75763 |
rs234026366 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71081604 | CCTAACCCCCCCACA[A/G]TAAGTACCTTCAGCC | 75763 |
rs234104307 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71074138 | AATATATCTATGCAT[A/G]TGTGGCTTGGGGCAC | 75763 |
rs234182066 | in-del | -/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71085533 | CTTCCTCATCCTCTT[-/C]CTTTCCTTTCCTTTC | 75763 |
rs234238837 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104346 | TTTTTTTTTTTAATG[C/T]TCTTTATTTGAATTT | 75763 |
rs234293238 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71062220 | TATAGAGCAGTCCTG[-/A]AAAAAATAAAGTTAA | 75763 |
rs234364209 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060570 | AATACTGTATTTACA[C/T]AATTTCTGCCTCACC | 75763 |
rs234420950 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71099903 | CAAATAAAAATCTAG[A/G]TACCTTGAGATAGTG | 75763 |
rs234507605 | in-del | -/AAAAAAA | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71090597 | AAAACAAACCAAAAG[-/AAAAAAA]AAAAAAAAAAAAAAA | 75763 |
rs234544784 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71093060 | AACTCTGCCTGCTTC[C/T]ACCTTTCATTGCTGG | 75763 |
rs234634137 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71100992 | ATAAAGACTTAAACA[A/G]TAGGGACACACTTAA | 75763 |
rs234715160 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091559 | TAAAACAAGAAAAGA[A/G]CAGTCAGAGCAGGTA | 75763 |
rs234721824 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71101896 | TTTCCCAGAACTATA[G/T]CGTTGATGGAGAAGA | 75763 |
rs234727669 | in-del | -/CACA | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71071295 | ACAGCAGATGCTCTT[-/CACA]CACACACACACACAC | 75763 |
rs234739655 | in-del | -/A | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111117 | GTATTAAAAAGGGGG[-/A]GGGGGTCAAAAGAAG | 75763 |
rs234804505 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71058068 | GGACAGATCCTGGCA[C/T]TCAGTCAGTCATAAC | 75763 |
rs234865185 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71101949 | TGGGGCTGTCTACAT[A/G]CTGGGTTCCAAGGTC | 75763 |
rs234891989 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059052 | AGAGTGTTTCTTTTT[A/G]TATCCACAAGTGCGC | 75763 |
rs235070221 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059101 | TAGAGTTACTGTGCT[G/T]TTAGGAAACACCATG | 75763 |
rs235098949 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71071992 | TTTCTACTTCTTTTT[C/T]TTTCTTAATTAGATA | 75763 |
rs235137902 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Dcaf17, Mettl8 | Mm_Celera | 2:71055516 | AGCGACACCACCAGG[C/T]GGCTGCACAGCACCC | 75763 |
rs235236043 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112689 | ctctttttcttttgc[A/G]gggggggggttgcaa | 75763 |
rs235248061 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111483 | TATAGATTTTGTTTT[G/T]TTTTGTTTTTTTGTT | 75763 |
rs235248224 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71102100 | AAAACAAAACAGCTA[A/G]GTGTGGCGACACACA | 75763 |
rs235270417 | snp | C/T | | | downstream-variant-500B | Dcaf17 | Mm_Celera | 2:71114830 | ATTTCTACCGAGTGG[C/T]CCAGGGACTCAAGGT | 75763 |
rs235327655 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71102645 | CTTGAATTTACATTG[A/G]TCAGAGCTGGGGCAG | 75763 |
rs235333638 | in-del | -/CAAAAAAAAAAAAAAC | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71071608 | CCCTGTCTTGAAAAA[-/CAAAAAAAAAAAAAAC]AAAAAAAAAAATTTT | 75763 |
rs235383332 | in-del | -/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71080137 | GCCACCATGTGGTTG[-/C]TGAGATTTGAACTCA | 75763 |
rs235414981 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71109392 | CCTTGTTAAGACTCA[G/T]GATACCTCCTCAAAA | 75763 |
rs235467063 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059639 | TGTTGCCTACAGCCT[A/G]ATCTTATAGACTTTT | 75763 |
rs235468089 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059472 | GTCCTGGAACTCACT[C/T]TGTAGACCAGGCTGG | 75763 |
rs235486800 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71110079 | AGTGTCAAAAAGCTT[G/T]TTGATACATGAAATG | 75763 |
rs235605399 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Dcaf17, Mettl8 | Mm_Celera | 2:71057068 | TCAGACTGAAGAGAA[-/C]CGACACAGTGAATTG | 75763 |
rs235637906 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71072968 | CAGCAAGTTCAGCAT[C/T]AGCCTGGGCTACCTA | 75763 |
rs235734306 | in-del | -/A | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091591 | TCACACCTGTAATCC[-/A]AGCACTCGGGGAGCT | 75763 |
rs235800815 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71095805 | CTCCCTATCGATGGG[C/T]TGTTTCTGCTATTTT | 75763 |
rs235868316 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71079495 | CTTGTCCCAAAGGGG[A/G]AAAAAAAGCAAAATG | 75763 |
rs235869946 | in-del | -/GCATTG | | | cds-indel, intron-variant | Dcaf17 | Mm_Celera | 2:71095621 | TTCTCAAAATTGAAA[-/GCATTG]GGTCATGCATTACCA | 75763 |
rs235885650 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71113432 | GAGTTCAATTCCTAA[A/G]ACCTACATGGTTGAA | 75763 |
rs235960772 | in-del | -/TGA | | | intron-variant | Dcaf17 | Mm_Celera | 2:71081295 | AAACATCAACTTGTT[-/TGA]TGATAATACTAGTGG | 75763 |
rs235994857 | in-del | -/A | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077660 | TCCAAGATACAGTAT[-/A]AATATTTTGTCCTTG | 75763 |
rs236002004 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71061161 | ATTTATTTATTTTGA[A/G]CACGTTCATGTATGA | 75763 |
rs236081855 | snp | C/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077506 | GTCCTCCTCTTATCC[C/G]TCACACATAGGCATG | 75763 |
rs236108086 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71061872 | CTTCAAGAGAAGAGA[A/G]CTTCTAGTCTGTAAC | 75763 |
rs236109008 | snp | G/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71094139 | ACAGAAAGCAAATCC[G/T]GTCACTGCTGCTATT | 75763 |
rs236271897 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71059588 | AGGGCCAGAGACATG[G/T]CTCAGTAGTTAAGAG | 75763 |
rs236296357 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71076433 | TATACTAAATTTTAC[A/C]AACTAAAGAATAATA | 75763 |
rs236383153 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077417 | GCTGCTAAAGTGGAA[A/T]ACTCCAAATTCAGAA | 75763 |
rs236386090 | in-del | -/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112808 | ATGCGAGCCACGTTA[-/T]TTTCGGAACAAAAGT | 75763 |
rs236511515 | snp | G/T | | | intron-variant | Dcaf17 | GRCm38.p3 | 2:71111586 | GCCTCGAACTCAGAA[G/T]CCGCCTGCCTCTGCC | 75763 |
rs236511708 | in-del | -/AAGGTCT | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71092364 | CCTGAGAATGGGTCC[-/AAGGTCT]AAGCATGAAGTTCGT | 75763 |
rs236581386 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71073163 | GGTCATCGCAGTGAA[A/G]TCGGCTCAGAACAAA | 75763 |
rs236590214 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71112761 | CATGATGTGAAAGTC[A/G]CAAAGAATCAATAGA | 75763 |
rs236600814 | snp | G/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71102782 | AAGCAGCTTGCTCCC[G/T]AAACACAAGGACAGA | 75763 |
rs236642546 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71100205 | TGGCTACTCTAACTT[A/T]TAGAAAAATTAAATT | 75763 |
rs236764322 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71085695 | GGATGGTCTCAGATT[C/T]ACAGAGATCTACGTG | 75763 |
rs236803257 | snp | A/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71077664 | AAGATACAGTATAAT[A/T]TTTTGTCCTTGTGAA | 75763 |
rs236986012 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098431 | ACATTTGAATAAATA[A/C]AATTAGGTCAAATAT | 75763 |
rs237011755 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71109329 | GAGAGGAGTCTCACA[A/G]ACCTTTGAACACGCC | 75763 |
rs237019935 | in-del | -/A | | | intron-variant | Dcaf17 | Mm_Celera | 2:71111581 | GCTGGCCTCGAACTC[-/A]AGAAGCCGCCTGCCT | 75763 |
rs237069445 | in-del | -/TTTTTT | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060124 | AACCATCTCTCTTGA[-/TTTTTT]TTTTTTTTTTAACAT | 75763 |
rs237083935 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71084262 | AATCCATGCCATCTC[A/G]GACTGTAAGTGTTCA | 75763 |
rs237101206 | in-del | -/A | | | intron-variant | Dcaf17 | Mm_Celera | 2:71060030 | CCCTGGAATTGGATT[-/A]CAGAGTTGTGAGCTT | 75763 |
rs237131005 | in-del | -/TTCGCAGC | | | intron-variant | Dcaf17 | Mm_Celera | 2:71098273 | TCCACAATAGCAATA[-/TTCGCAGC]TTCTATACCTACCAC | 75763 |
rs237168652 | snp | A/T | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71063121 | GGGGCTTGTGCACCC[A/T]CAGGTACACAATGAT | 75763 |
rs237191549 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71071777 | TTCCAAGAATTTGTT[C/T]TTACATACTGCTCCC | 75763 |
rs237249475 | in-del | -/A | | | intron-variant | Dcaf17 | Mm_Celera | 2:71086076 | TAAAATATAATCCTT[-/A]AAAAAAATGGAATTG | 75763 |
rs237400904 | snp | C/T | | | intron-variant | Dcaf17 | Mm_Celera | 2:71081447 | GCTGTTAGCCTATAA[C/T]ATGGAAGGTCTCTCT | 75763 |
rs237401096 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Dcaf17 | Mm_Celera | 2:71091629 | GAGGATTGCTGCAAA[C/T]TTAAGGCCAACTTGT | 75763 |
rs237415786 | snp | A/C | | | intron-variant | Dcaf17 | Mm_Celera | 2:71078914 | AATGAAGGTCAGCAA[A/C]ATTCTACCCATTCAT | 75763 |
rs237520926 | snp | C/G | | | downstream-variant-500B, intron-variant | Dcaf17 | Mm_Celera | 2:71099464 | ACTCCTCCATGGACG[C/G]CGCATCAGTTCCTGC | 75763 |
rs237535638 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dcaf17 | Mm_Celera | 2:71064452 | CAAGTTGTGGGATTT[C/T]AGGCATCCATAGCAC | 75763 |
rs237545295 | snp | A/G | | | intron-variant | Dcaf17 | Mm_Celera | 2:71104274 | GACTTGAAGTCTGGC[A/G]CCTAGCCCAACATCC | 75763 |