| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs243268911 | snp | A/G | | | utr-variant-3-prime | Nfx1 | Mm_Celera | 4:41025893 | CCTCCTGAGTGCTGG[A/G]ATTAAAGGCATGCGC | 74164 |
| rs243275814 | snp | A/G | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969414 | CCTTTGCTGTGCTCC[A/G]AGGTTCTGGAGTACG | 74164 |
| rs243286898 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41017420 | CTGGGCAGCCATATG[A/G]TTGTACAAGGATCTG | 74164 |
| rs243289453 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40991692 | GAAGGGCTTGGGCTT[C/T]AGTCTGTGTAGTGGG | 74164 |
| rs243429280 | snp | A/G | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40970176 | GGGGGGAGGGGGGGG[A/G]CGCTTGGGGGCGTCT | 74164 |
| rs243443311 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41017963 | TCAATCCTTTTTTTT[A/T]AATTTCAGAATAGTT | 74164 |
| rs243450108 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41001664 | CACTTTATCGATGTA[C/T]TGCATATTCTTTATC | 74164 |
| rs243498224 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40984282 | GGTGTAGTGGTGCAT[A/G]TCTGCAGTTGGAGCC | 74164 |
| rs243529440 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Nfx1 | Mm_Celera | 4:40970896 | CGCCATTTCACTGTG[C/T]GCTCAGGTAGCACCA | 74164 |
| rs243533245 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40981217 | GTTAGGATTAAAGGC[A/G]AATACCACCACTCCT | 74164 |
| rs243627787 | in-del | -/A | | | intron-variant | Nfx1 | Mm_Celera | 4:40980431 | CACTGTCAGTGCTGT[-/A]ACCTACCTACTAAAG | 74164 |
| rs243662656 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40989194 | TTCCATTTGCCTTCA[A/G]TTGTCAAAGGATTAC | 74164 |
| rs243698778 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40997190 | AAGGCCAGTGGGCCC[A/G]GGACCACTTACAACG | 74164 |
| rs243752685 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41006544 | AGGTCCTAAGGATCA[C/G]TCTCAGGTTGTTGGA | 74164 |
| rs243781317 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40998858 | TGAATTCAAAGCCTG[C/T]CTCAGCTCTGAAATG | 74164 |
| rs243786582 | in-del | -/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41022723 | TTGAAAACATGCAAG[-/C]CCCCCCCCCCACCAG | 74164 |
| rs243816648 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41007525 | TACTCCCCCAGATAG[A/G]GGATCCACAACAGAT | 74164 |
| rs243820549 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40989881 | AACCCTGGGATCTAC[A/T]TGGTGAAGGAAGAGA | 74164 |
| rs243869746 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41009592 | TGCCATACCAGACTT[A/G]CATGCACACACACAG | 74164 |
| rs243870933 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41023235 | TTTCCCTCGCCTACT[A/T]CGCCTCCCTCAGCTC | 74164 |
| rs243908021 | in-del | -/TGTT | | | intron-variant | Nfx1 | Mm_Celera | 4:41020486 | GTAGCACTATCCAAG[-/TGTT]TGTGTCCCTTGCAAT | 74164 |
| rs243934230 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41023803 | GCTAGCTCTTCAGCA[A/G]GACAGGCAAGACACT | 74164 |
| rs244034365 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40985963 | TCGGAAGAGCAGTCG[G/T]GTGCTCTTACCCACT | 74164 |
| rs244116711 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40972157 | AACAGGAGGATCTTT[C/T]GAGTTGGAGTCCAGC | 74164 |
| rs244162856 | snp | A/C | | | utr-variant-3-prime, intron-variant | Nfx1 | Mm_Celera | 4:41013765 | ATTTTACCCCCCCCC[A/C]AAAAAAGTCATCTTT | 74164 |
| rs244239835 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41006361 | CTTCTGCCTCTGTGT[C/T]GGTTGCTGAGGTTAC | 74164 |
| rs244308034 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41019891 | CTATTGTGTTTATGT[A/G]TCTGTGTGAATGTAT | 74164 |
| rs244376868 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40979302 | CCATAGATTACATAC[A/G]TGACAGTGCGACTAG | 74164 |
| rs244394674 | snp | A/C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41008143 | ACTAAGAAAAAAATA[A/C/T]TTGTTTTTTGAGACA | 74164 |
| rs244402986 | in-del | -/CATC | | | intron-variant | Nfx1 | Mm_Celera | 4:40990963 | TGGTAGGTATAAAGT[-/CATC]CATCCCCTGCTATCC | 74164 |
| rs244503782 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40975713 | GAGAGAGACTGCATA[C/T]TCACTGTGCTAATAC | 74164 |
| rs244568905 | snp | A/C | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Nfx1 | Mm_Celera | 4:41011793 | GAGAGACCCCACAGT[A/C]CTGGAGATGCCAGAA | 74164 |
| rs244602933 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40983876 | ATTACTCTGTGTCAA[A/G]CAGGTCACAAACTTG | 74164 |
| rs244608574 | in-del | -/ACACACACACAC | | | intron-variant | Nfx1 | Mm_Celera | 4:41010490 | TGGCACATGTGCATT[-/ACACACACACAC]ACACACACACACACA | 74164 |
| rs244673570 | in-del | -/CC | | | intron-variant | Nfx1 | Mm_Celera | 4:40988173 | ATCCCACAGCCTCTT[-/CC]TGGTCCAATCCCTTT | 74164 |
| rs244717656 | in-del | -/GGTCATCT | | | intron-variant | Nfx1 | Mm_Celera | 4:40976148 | TTTGGGTAAATGCTA[-/GGTCATCT]GTGGCTATCAGTGTC | 74164 |
| rs244769118 | in-del | -/CTGC | | | intron-variant | Nfx1 | Mm_Celera | 4:40982278 | TGTAAACCTTAACAG[-/CTGC]CTGTAGAGAAGAGTG | 74164 |
| rs244798928 | in-del | -/CAAT | | | intron-variant | Nfx1 | Mm_Celera | 4:41006500 | AGGTCAGGGGACAAC[-/CAAT]CTTCAAGAATTGGTT | 74164 |
| rs244807539 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40974053 | TTCTCTATGGCCTTT[A/G]TGAACTCACCAGTTC | 74164 |
| rs244846273 | snp | A/G | | | utr-variant-3-prime | Nfx1 | Mm_Celera | 4:41025472 | GGGACCAGCTCTCTC[A/G]CCATGTTCACAATGT | 74164 |
| rs244854713 | in-del | -/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40998592 | GCTTGCCTATCTCTG[-/C]CTCCCAGGTGCTGGG | 74164 |
| rs244870850 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40995089 | TAGGATTTTATTACA[A/G]GCTTTCTGAGGCTTT | 74164 |
| rs244894894 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41003194 | GAAATCAACTGGAGG[A/G]GCCCTAAACGGCCAT | 74164 |
| rs244902033 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40994513 | CTTTTACTCAAACTA[A/C]ACTTGTGAAAATACA | 74164 |
| rs245053282 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41001306 | TTGGGAGGAGAGCAG[G/T]GTTGAGGATGGTTCT | 74164 |
| rs245112871 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40972900 | AATACAGTTCCTCAG[A/G]TTGTGGTGACCCCAA | 74164 |
| rs245143865 | snp | G/T | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40992787 | CACTTGAGGTTTTCC[G/T]CTTGCCATGTGCTAG | 74164 |
| rs245145289 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41000930 | CCTTAGAAAATGTTA[C/T]AAGTTGTGGGTGCAA | 74164 |
| rs245204303 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40984735 | GGCTTCTATCAGCCA[C/T]ATCTGCCCTTTTTTA | 74164 |
| rs245269947 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40973776 | ATTCAATATGAAACG[C/T]CCTTTATCAGGCTTT | 74164 |
| rs245317748 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40975532 | CCTCTGCCCTGGCAG[C/T]TGATTTCCTTGGGTT | 74164 |
| rs245327136 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41008396 | TTCTTCTGTTTGTCT[A/G]TGTGTGTCTTTCTAA | 74164 |
| rs245333575 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40976238 | AGACCAATCTCATCA[A/T]GTCTGTTTTATTCAC | 74164 |
| rs245336003 | in-del | -/TC | | | intron-variant | Nfx1 | Mm_Celera | 4:40977450 | GATAACACAGTGAAA[-/TC]TCTACCTGCTTGGAT | 74164 |
| rs245350431 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40974597 | CTCATTGGAGTCTGA[A/G]TTCAGATAGTCCATA | 74164 |
| rs245352054 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40985164 | GCCTGGTCTCTAGAG[A/T]GAGTTGCGGGACAGC | 74164 |
| rs245365157 | in-del | -/GT | | | intron-variant | Nfx1 | Mm_Celera | 4:40984454 | TGGAGACAGGAAAAG[-/GT]GTGATTTTATAAAAT | 74164 |
| rs245473212 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41008649 | CAGTGTTTTCTATGG[A/G]TGGGTGGTTTGCCTT | 74164 |
| rs245502690 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41001425 | CACTTAGGATGTTAT[A/G]TAACATCACTCTGTC | 74164 |
| rs245523846 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41000614 | TGTGCATGTGTTCAC[A/T]AACAAAAGCACAAAT | 74164 |
| rs245561516 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41009820 | AGCCACCTCTAACCC[C/T]GCAGCATCTTAATCT | 74164 |
| rs245581624 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41002211 | TCCTGCCTAAACCTT[C/T]TGAGTTCTGGGATTA | 74164 |
| rs245595926 | in-del | -/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40988302 | TTCTTTCCTTCTGAT[-/C]TTTACCACAGATACT | 74164 |
| rs245610622 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41010003 | AAGACGGCTTAGTGG[A/G]TAAGGGCACGTGGTG | 74164 |
| rs245681654 | snp | C/T | | | synonymous-codon | Nfx1 | Mm_Celera | 4:41023625 | CCAGGGCAAGAATAA[C/T]AAGAAAAGCCACTGC | 74164 |
| rs245749886 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40982830 | GTTTTGCACATTAGA[C/T]ATGCTTTGATAAAAC | 74164 |
| rs245754509 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41020439 | CACACTGAATAAACT[C/G]CACACAGGCATCTCA | 74164 |
| rs245762987 | in-del | -/AAA | | | intron-variant | Nfx1 | Mm_Celera | 4:41014720 | CCACCCCATCCCCCC[-/AAA]AAAAAAAGAAAGCCA | 74164 |
| rs245807186 | in-del | -/GTT | | | intron-variant | Nfx1 | Mm_Celera | 4:41002417 | CTTTTTAAAAGCTGG[-/GTT]GTTCTTTCTGTTGTC | 74164 |
| rs245898650 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41016844 | ACCTGAGTTCGGATT[C/G]CAGGCAGCTCCTGAT | 74164 |
| rs246196505 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41016288 | AGCCCGAGGAGGTTG[C/G]TGGGTTTCTTGTTAT | 74164 |
| rs246218544 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41008601 | TGGATGGCAAGAAAA[C/T]ACTCAGTGGCAGCAT | 74164 |
| rs246223870 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40988615 | TCTCCCATTTGATCT[G/T]TTGTAGGCAAAGTAA | 74164 |
| rs246255575 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41008326 | CACACGCAGGATTAT[A/G]GGTGATGTGCAAATC | 74164 |
| rs246259527 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40985079 | TGTCTCCTGGGTGGA[A/C]ACAGTAATGCACACC | 74164 |
| rs246272305 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40980666 | GGGTTGACCCTGGGG[C/G]ACCCGCATGCTACCC | 74164 |
| rs246275787 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40996370 | TGCAGGCCAAGAGGC[A/G]AGAAGATTATGACTT | 74164 |
| rs246299471 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40992655 | CACCACATGGGGGCT[A/G]AGGAATCAAACCTAG | 74164 |
| rs246581396 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41009927 | GCAGTGTCTTCTCTG[A/T]CCTGGTGAACCGTGT | 74164 |
| rs246606845 | in-del | -/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40977587 | TATCCCCATATCTTT[-/C]TTTTTTTTTTTTTGA | 74164 |
| rs246620253 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41018848 | CATGCGGCCTGAGGC[C/T]CAGTCCCGGGTACAA | 74164 |
| rs246632212 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41022542 | GTATATTAAGAATAA[C/T]CCTCAGTTGGACATG | 74164 |
| rs246934247 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40978083 | TTGCCTTACTCTGCC[A/G]TCTTATTGCACAGTC | 74164 |
| rs246950412 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40986162 | CCTACCTGATTTACC[A/G]CGTCAGTAAGTCTGG | 74164 |
| rs246976743 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40986572 | CTAGAGCCTTGTGTA[A/G]ACAAAGCCATTCCCT | 74164 |
| rs247016919 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40977478 | GGATTCCACAGTGAC[C/T]CATTGCTGTTCTCAA | 74164 |
| rs247030755 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41009946 | GGTGAACCGTGTCCC[A/G]GCCCCCAACACAAAG | 74164 |
| rs247124865 | snp | C/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969226 | AGAGAACCAACTTTC[C/T]CAAGTTGTGTGATGA | 74164 |
| rs247125439 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40980459 | AAGACCCTTCCCCTC[A/G]TAAGGATAAGGAAGT | 74164 |
| rs247157448 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40978463 | ATTAACCCCTCCTCA[A/G]GCTAAAGGTATATAT | 74164 |
| rs247161057 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40988976 | TTACTGTGCTAGGAT[A/G]TGATGGAGCTGGGTG | 74164 |
| rs247209302 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41022143 | GGTCTGGCAACTCCT[C/G]TCTTCTGCACTTTAT | 74164 |
| rs247212055 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41010893 | AAATTACTTAGACCA[A/G]GTTGGCCTGTAGCTT | 74164 |
| rs247235420 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41020473 | GTCACCTCAGCTCGT[A/G]GCACTATCCAAGTGT | 74164 |
| rs247257812 | snp | A/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40970007 | AACAAGACCTGAAGT[A/T]AAAGTGGTTTATTGG | 74164 |
| rs247307734 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41011062 | ACTGAGCTCCTCTAA[C/G]CTCTCTGCCATAATG | 74164 |
| rs247342034 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41003552 | CCCAAGACAACTTCA[A/G]ATTAGAATGGTCCTT | 74164 |
| rs247353016 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41011212 | AGCACTGAGTAGTGA[C/G]GTTGAGGCTGTGATA | 74164 |
| rs247353672 | snp | A/G | | | utr-variant-3-prime, intron-variant | Nfx1 | Mm_Celera | 4:41013138 | GCCTCTGTGTCTTAG[A/G]TACTGGGATTACAGG | 74164 |
| rs247356378 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41022763 | AATGTTGCCTGTGAG[A/G]GAGCACACTCTTATT | 74164 |
| rs247381191 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41005145 | GCTATCCCGAAATTC[C/T]CCTAAACCCTCCCCC | 74164 |
| rs247421634 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41003986 | AATTCACACACGCAC[A/G]TGCACCCTTAAATAC | 74164 |
| rs247423253 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41014212 | CCCTGCAGCAGTGCC[A/C]AGTGTATCCCCATCC | 74164 |
| rs247512457 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40980204 | ATTAAAAGTGTGTGC[C/T]ACCATGCCTAACTTT | 74164 |
| rs247540747 | snp | A/G | | | downstream-variant-500B | Nfx1 | Mm_Celera | 4:41026315 | GTGATTTGTGCATGC[A/G]AGAAAGGGAACTCTG | 74164 |
| rs247717876 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41001914 | CAGTTTTTAAACAAG[C/T]TTTTACTTAAATGTG | 74164 |
| rs247726857 | snp | C/T | | | upstream-variant-2KB | Nfx1 | Mm_Celera | 4:40970418 | CCTACCGGTTTGTGG[C/T]TCATTTGCTATTAGT | 74164 |
| rs247759762 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40994385 | AGATTTTATTTTTTT[A/T]AAAATGTAAATGTTT | 74164 |
| rs247759879 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40985301 | AGCCAAAAATATGAA[A/G]GGCATAATAATGAAA | 74164 |
| rs247794227 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40993204 | GGGATCAAAGGCGTG[C/T]GCCATCACGCCCGGC | 74164 |
| rs247859994 | in-del | -/CC | | | intron-variant | Nfx1 | Mm_Celera | 4:40995553 | GTTCCATCCTCAGCT[-/CC]ACACACTCCACACAC | 74164 |
| rs247903481 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41006148 | TTTTATGTATATTCC[C/T]TTTTTTCTAAAAATG | 74164 |
| rs247956753 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41020230 | AGGGTGTCAGGTCTT[C/G]TGACCTGGAATAGTA | 74164 |
| rs247963411 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41019475 | TTTTCATTTTAGTCA[A/G]CACTTGTGACTGTAT | 74164 |
| rs248044506 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41019913 | TGAATGTATGTCTCA[C/T]ATGTACAGGTACCTG | 74164 |
| rs248059057 | in-del | -/AT | | | intron-variant | Nfx1 | Mm_Celera | 4:41002677 | GTGTATATATAAAAC[-/AT]AGAGCTACATACTGT | 74164 |
| rs248074510 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40997435 | TTAGAATGTATATTG[C/T]CATCCTGGTATGGCC | 74164 |
| rs248160814 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41011168 | GCAGTATACCTAAGT[A/G]ACACATAAATGAGTC | 74164 |
| rs248194424 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40972497 | AAAGAGTGCAAGAAC[A/G]CATTGCATTGGTGTG | 74164 |
| rs248194978 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41010838 | AACACAACTGATTTT[A/T]TATATATATATATTC | 74164 |
| rs248239431 | in-del | -/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40980704 | TGGTGTGTTTGTGTA[-/T]TGTGTGTGGTGTGTA | 74164 |
| rs248245685 | snp | A/G | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40968776 | TATCATCTTTCTGGT[A/G]TATATATATATATAC | 74164 |
| rs248321349 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41023584 | GATCCCAGGGCATGG[A/G]AATGATCAGTCTTCT | 74164 |
| rs248412137 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41019842 | TTATGCGTCTGTGTG[A/G]ATGTATGTCTCACAT | 74164 |
| rs248444071 | in-del | -/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40972412 | GAATTACAATTGCAC[-/T]TCTGACAGATTGATG | 74164 |
| rs248464320 | snp | A/C | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40970349 | AAAAAAAAAAAAAAC[A/C]CAGTAACTTCAAACT | 74164 |
| rs248486501 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40999388 | TGCTCATCTTCAATA[C/T]CCACTCTTACATCTG | 74164 |
| rs248514300 | in-del | -/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40997953 | ATTTGGAAGATGTAA[-/T]TAGTTTAATGGATAA | 74164 |
| rs248585530 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40995940 | AGGCCAACTAGGTCT[A/G]TTACATACATTGACA | 74164 |
| rs248676135 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40998289 | TCTCTCCAGCAGTCC[C/T]GTCTCTGCTTTCTTG | 74164 |
| rs248678377 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40989527 | GTGTGGAACATTATC[A/G]TGTGGAAGCCAGAGG | 74164 |
| rs248712528 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40997389 | ATAGAGAGAATATTC[A/C]AGCCAGGAAGGTTCA | 74164 |
| rs248725953 | in-del | -/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41021962 | GCCAGGTAAAGTAAG[-/C]CTTATGATGTAAGAA | 74164 |
| rs248808112 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40988105 | TGCAGCCCCTTTATG[C/T]CTCCTGGGAAGCTTC | 74164 |
| rs248840996 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40990327 | GTAGTCTTGGTAGAC[A/G]TGAGCACTGTTGGCT | 74164 |
| rs248859959 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40988135 | CGGAACCAGGCTCGT[C/T]GTGTGTGGGTTTCTG | 74164 |
| rs248875475 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40990182 | CTCTTGCCCCTGTGC[C/T]GGGATTACGGACCAC | 74164 |
| rs248917910 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40979670 | CACAACTCTTGAAAC[A/G]TAGTTGTTAGTCAGC | 74164 |
| rs248932886 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40981647 | AGATCTTCTTACCCC[C/T]GCCTCCCAAGTGCTG | 74164 |
| rs248950100 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40990642 | AATCTGATGACTGCA[A/G]TCCTCTTCCCTGTTG | 74164 |
| rs248951059 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41024271 | TGAAGGGTGGCGTTG[A/G]AGGAGGTGGGCTGCA | 74164 |
| rs249058667 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41016455 | CATTGGGGGGAGTTG[A/G]CTTTCTCCCTCTACT | 74164 |
| rs249107078 | snp | C/T | | | utr-variant-3-prime, intron-variant | Nfx1 | Mm_Celera | 4:41012658 | CAGAAATGGCAAGGG[C/T]CCTGTGACTGATGTA | 74164 |
| rs249251939 | in-del | -/TGTGTG | | | intron-variant | Nfx1 | Mm_Celera | 4:41016355 | TATTTATTTATTGCC[-/TGTGTG]TGTGTGTGTGTGTGC | 74164 |
| rs249330519 | snp | C/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, missense | Nfx1 | Mm_Celera | 4:41011738 | CTACAGAGAGTCGTG[C/G]AGAAGCCATTGGTGA | 74164 |
| rs249345121 | in-del | -/CC | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40970321 | CCCTTTCCCCACTCT[-/CC]CCCCCCCCCTCCAAA | 74164 |
| rs249365413 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40981479 | CCCCCTTCTCCACCT[C/T]CCCCAGATATACTCT | 74164 |
| rs249426790 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40971854 | AAATGTGAACCGAGA[A/G]GCTGGGGCGCTAGTT | 74164 |
| rs249435239 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41002915 | CACCATTAATTTATT[A/T]ATATTACGTTTGTAT | 74164 |
| rs249458679 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41005974 | TGTGTGTACATGAGT[A/G]AAGAGGCCAGAAATC | 74164 |
| rs249463843 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40997506 | TGTGTGACCAAAGCC[G/T]CAAGCCTAAAACTGT | 74164 |
| rs249485978 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41004726 | ATAATGAAGGTAGGG[C/G]GAACAATTAAATCAC | 74164 |
| rs249547874 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40989741 | CTTCCTTAGTGCTGG[C/G]ATTGCAAGTGTGAGC | 74164 |
| rs249570997 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40995593 | TAGAGGCAGAGAATT[C/T]TGCAGTTCATAGTTA | 74164 |
| rs249603027 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41003473 | CTGTGGGCCAGCTGA[A/C]ATGGCAACTGGCAAC | 74164 |
| rs249606586 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40997288 | AGAATTAGTCGATTG[A/T]AAAAACATGTAGGAA | 74164 |
| rs249649478 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41007771 | TGTCTCCTCCAGGCA[A/G]CTGGCCTTGTGTCGG | 74164 |
| rs249684376 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41015052 | GCTACAGTGTTTACC[C/T]AGAATGCCTTCCTGA | 74164 |
| rs249687635 | in-del | -/G | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40970125 | AGAGAGAAGGGGACC[-/G]GGACGCTGACAATAG | 74164 |
| rs249733604 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40996197 | ATGTGGACTGGCAGT[A/G]TAACTCCTCAGTAGA | 74164 |
| rs249799630 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40988365 | TTAATAAGTATTTTT[A/T]AAAAATAGATTGTGT | 74164 |
| rs249811822 | in-del | -/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41007143 | GGTGACCCCTAACCA[-/G]GAAATTATTCTCACT | 74164 |
| rs249822893 | in-del | -/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41017858 | TTAATAATACGGTTT[-/C]CCGAGGTCACACAAA | 74164 |
| rs249866842 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41010517 | CACACACACGTCATT[C/T]ATTTTTATTATTTAT | 74164 |
| rs249965218 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40973825 | TTTATCTAGCCCCCT[C/T]CTCCATCCTTGCTTC | 74164 |
| rs250004629 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40983509 | TAGACAAGAGGCTAC[A/G]GAGGTGACTCCACAT | 74164 |
| rs250031764 | snp | C/T | | | synonymous-codon | Nfx1 | Mm_Celera | 4:41022281 | CTTAAAGTTTGTCAG[C/T]GACGTTGAGAAGGAA | 74164 |
| rs250158693 | in-del | -/GT | | | upstream-variant-2KB, utr-variant-5-prime | Nfx1 | Mm_Celera | 4:40970820 | CTCCTCCAGCCACTC[-/GT]GTCCCCCCCGCAAAC | 74164 |
| rs250239560 | snp | C/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969874 | GTGCTGGAATTAAAG[C/T]CTAAGTCACCACACC | 74164 |
| rs250253990 | in-del | -/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40981611 | CCTGGAGCTCACTCT[-/G]GTAGACCAGGCTGGC | 74164 |
| rs250286730 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41008786 | TAAGAATTGAACCTG[C/T]ATCCCCTGGAAGAAC | 74164 |
| rs250292736 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40979339 | ACTAGTTAAAAAAGA[A/G]AATGCTTTCCTTTTT | 74164 |
| rs250357177 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40974730 | ACATATAAGAAAAAA[A/G]GGGGGGCTGGTGAGA | 74164 |
| rs250401187 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40974029 | CAAAGCCTGGATTGA[A/G]TGTGAGGTTTCTCTA | 74164 |
| rs250465897 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41014305 | TCATAGAGGTTGGAG[A/G]GAGGGAAGTTAGAAT | 74164 |
| rs250506770 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41022960 | TTCTGTGAGTTGGAG[A/G]ACAGCCTGATCTACA | 74164 |
| rs250588562 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40996719 | TGCTGGGTGGAGGGA[A/C]GCTGAGGATGAGGAC | 74164 |
| rs250615130 | in-del | -/CA | | | intron-variant | Nfx1 | Mm_Celera | 4:41005661 | GTGCACACGTACATG[-/CA]CACACACACACACAC | 74164 |
| rs250625307 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41001808 | AGCCAGGATGTCTAC[A/G]CTCAAGCTGGCCTCT | 74164 |
| rs250631280 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40992663 | GGGGGCTGAGGAATC[A/G]AACCTAGATCCTCTT | 74164 |
| rs250652728 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41005049 | TAGGTATGTGTGATC[A/T]AAGCCACATGGTGCC | 74164 |
| rs250663462 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41000788 | ATACCCTGCTCTTCT[A/G]ACTTCCATAGGCACC | 74164 |
| rs250729904 | in-del | -/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41010588 | CACCAGGCATTAGAT[-/C]CCCATTACAGATGGT | 74164 |
| rs250775094 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40982602 | AGTTATTTCAGTGGG[C/T]GTGTCATTTGACTGG | 74164 |
| rs250792433 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40993441 | CCCTCTGCATCTCAG[C/T]CTAGCTTGCCGGCAC | 74164 |
| rs250810702 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40990756 | ATACACAGAAATGGC[C/T]TACCTCATTGAAGCT | 74164 |
| rs250812266 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40991527 | GAGCTGGTCACTCCA[A/G]CTCTGGGGACATGAC | 74164 |
| rs250867884 | in-del | -/TGGACGTATC | | | intron-variant | Nfx1 | Mm_Celera | 4:40983324 | TAAGGGGCTGAGCCA[-/TGGACGTATC]TGGCAAGTCTTCTCA | 74164 |
| rs251088021 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41016385 | CGCGCGCGCATGTAC[A/G]TGTATATGTGTGTAC | 74164 |
| rs251088729 | in-del | -/ATTTTTTT | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41000964 | AGGCTGGATTGATTG[-/ATTTTTTT]TTTTTTTTTTTTTTT | 74164 |
| rs251107747 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40983621 | GGTTGCAGGGTATCT[A/G]ACATTTTCTTCTAGC | 74164 |
| rs251110101 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40973261 | CTACTACTTAAAATA[C/T]TGAAATGTGTCTCAC | 74164 |
| rs251144121 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40982812 | GAATTCCACAGCTAT[A/C]TTGTTTTGCACATTA | 74164 |
| rs251167601 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40980900 | AAACAGCCTCATGTA[A/G]CCCTGACTGGCCTTG | 74164 |
| rs251168143 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40973905 | CACTTGTAAGTTTAT[A/C]TCATCTTCCCAGAAT | 74164 |
| rs251227831 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41024320 | AGACAAACAAAGTGG[C/G]ATGCAGGTTGGCCAC | 74164 |
| rs251255504 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41016817 | TTAAGAGCACTCATT[A/G]CTCTTCTGAGAACCT | 74164 |
| rs251260312 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40992121 | TAGCATCTTCATACA[A/G]TGTTGACAGGTGTTT | 74164 |
| rs251274810 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40972102 | CAGTGCTATCAGACA[G/T]GGTAGCGCACATCTT | 74164 |
| rs251308568 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40971343 | TTCCCGAGGCCGCGC[A/G]GAGCAGAGTCCGGCG | 74164 |
| rs251412806 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41008487 | GTTCTCTTCAAAACC[C/G]GTGCGTGTAGATGGG | 74164 |
| rs251413915 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41017545 | GATGTCTGATTGGCT[A/G]TTGGTTGCTTTTGTT | 74164 |
| rs251424269 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41007167 | TCTCACTACTATGTC[A/G]TTACTATAATTTTGT | 74164 |
| rs251525550 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41007341 | CCATATTATGTTATT[A/G]GATATTTGTTTTTAG | 74164 |
| rs251540740 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41018348 | CCTCCTAACTGCGCC[C/T]GGGCCTAAGCTGATG | 74164 |
| rs251571791 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41008060 | GCCACACTAAGTCTA[A/G]CCGTGTGGTTTGAAC | 74164 |
| rs251602910 | snp | A/G | | | missense | Nfx1 | Mm_Celera | 4:40977198 | AAGTCAGCCTGTGAC[A/G]CTGGGAATTTGGCAG | 74164 |
| rs251642993 | in-del | -/TTA | | | intron-variant | Nfx1 | Mm_Celera | 4:40973340 | CTTTTAAAGATTTAT[-/TTA]TTATATTTAAGTACT | 74164 |
| rs251672360 | in-del | -/TA | | | intron-variant | Nfx1 | Mm_Celera | 4:40985819 | ATTTTTTTTTTTTTT[-/TA]AAGATTTACTTATTC | 74164 |
| rs251694725 | in-del | -/TTAGA | | | intron-variant, downstream-variant-500B | Nfx1, Mir3094 | Mm_Celera | 4:40993882 | TTCCTTTTTTTACCT[-/TTAGA]TTAAAGTTTCTTTTA | 74164 |
| rs251715552 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40999854 | CATTTATAATTCTTA[C/T]GGTAAAAGGAGAAAA | 74164 |
| rs251736894 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40991569 | CCATGGCCACCTGCA[C/T]ACCTGTTTACAAACA | 74164 |
| rs251777287 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41000066 | GCCTCTAACAGCATT[G/T]CAGGCCCACCGGCAT | 74164 |
| rs251872945 | snp | A/G | | | utr-variant-3-prime | Nfx1 | Mm_Celera | 4:41025294 | ACTATGTCTGCAATC[A/G]TGTGTCTTAAACCTA | 74164 |
| rs252014660 | in-del | -/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40990088 | TTAGTAATTTTTTTT[-/C]CTTGTTCTAGCTTCT | 74164 |
| rs252015978 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40978528 | TATGTATGTGTACTA[C/T]GAGTGTGCCTGGTGC | 74164 |
| rs252029977 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40999574 | ACACTGACATAATTG[A/G]GGCAGCTCCAGGCTG | 74164 |
| rs252057808 | snp | A/G | | | downstream-variant-500B | Nfx1 | Mm_Celera | 4:41026089 | AGCCTAAGTGCTGGC[A/G]TTGCAGGCTCTCACC | 74164 |
| rs252080736 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40987175 | CCTGTCTTTGGTTCC[A/G]TGCTAGACTTAGACA | 74164 |
| rs252113676 | in-del | -/TGTG | | | intron-variant | Nfx1 | Mm_Celera | 4:41016356 | TATTTATTTATTGCC[-/TGTG]TGTGTGTGTGCGCGC | 74164 |
| rs252175749 | in-del | -/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40972909 | CTCAGGTTGTGGTGA[-/C]CCCCAACCATAAAAT | 74164 |
| rs252176299 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40991381 | GAAGGAGGGAAGGGA[A/G]GCAGTGAGGAGAATA | 74164 |
| rs252180133 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40979949 | GAGTTTGAGGATAAG[C/G]TGTAGTACTTGTCCA | 74164 |
| rs252180146 | snp | A/G | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969627 | CCGATTTTCAAATAT[A/G]ATTCCTGAAGGATTC | 74164 |
| rs252218569 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40979057 | TTCCTGGTTGGTGTG[A/G]AAGTCCCTGTTTAGA | 74164 |
| rs252239572 | snp | C/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40970254 | GTGGTTGCTAGGGTC[C/T]TGGGGGCAGGCCAGC | 74164 |
| rs252304469 | snp | A/G | | | downstream-variant-500B | Nfx1 | Mm_Celera | 4:41026024 | TTGAGACAGGATCTC[A/G]CTAAGTTGCTTAAGC | 74164 |
| rs252329409 | in-del | -/CT | | | intron-variant | Nfx1 | Mm_Celera | 4:40986682 | CTTCTCCCCCCCCCC[-/CT]CCCCTCCAGATGGCC | 74164 |
| rs252407080 | in-del | -/CT | | | intron-variant | Nfx1 | Mm_Celera | 4:41003509 | TGTCCTCTGTAAAGA[-/CT]CTAACTATTGAGCCA | 74164 |
| rs252498271 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41004186 | TCTGCTCAGTCTCGG[C/G]GTCCCTGGTTCCCCT | 74164 |
| rs252547731 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41007946 | GAACTTCCCTACAGG[A/G]TGGGATGTTTCTATC | 74164 |
| rs252557169 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41011382 | TTGAGGTTTCCAAGG[A/G]AAACAAGAACTTTAT | 74164 |
| rs252616994 | in-del | -/TTCCTTCCTTCCTTCCTTCCTTCC | | | intron-variant | Nfx1 | Mm_Celera | 4:40998699 | TTGAACAAGTGTTGT[-/TTCCTTCCTTCCTTCCTTCCTTCC]TTCCTTCCTTCCTTC | 74164 |
| rs252637929 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41019213 | TGACTTTGGACTCCC[A/T]ATATAGGCTATGCCT | 74164 |
| rs252642072 | in-del | -/ACAA | | | intron-variant | Nfx1 | Mm_Celera | 4:40985683 | CATAGTAAGACCTTG[-/ACAA]ACAAACACCCAGATA | 74164 |
| rs252709726 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41001685 | ATTCTTTATCCATTC[A/G]TTAGCTGATATCTAT | 74164 |
| rs252729016 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40985613 | ATCCCAGCACTTGGG[A/T]GGGGAGTTTGAGGCT | 74164 |
| rs252755069 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40993563 | ATCTTCTGCAGCAGC[A/G]CTAAGGCACTGGCAG | 74164 |
| rs252766107 | in-del | -/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41004172 | CTCCAGGGAGTGCTC[-/T]TGCTCAGTCTCGGGG | 74164 |
| rs252799191 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40994960 | AAGATAATTTCATTT[A/G]CATTGTTGATTGATC | 74164 |
| rs252819848 | in-del | -/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41019683 | TCAGATATCAGAATA[-/G]GGGCCTAAGATTCCT | 74164 |
| rs252837373 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40986345 | CTTTCTTAAATGTCT[A/G]ATAATAGTATTTTTA | 74164 |
| rs252859715 | in-del | -/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40986386 | TTCTATAAGTTTACC[-/T]TTTTTTCTCTTTTTT | 74164 |
| rs252864690 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40986948 | TTCTAGATTTAAGGA[A/G]CATGAGTAAAAATGG | 74164 |
| rs252890671 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40987355 | AGGTTTTTGCATCTG[C/T]CTTTGTTGTCTCACT | 74164 |
| rs252920880 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41020343 | TCCAGCCCCCGTTGC[A/G]CACTGTGTGAAGTAA | 74164 |
| rs252964731 | in-del | -/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40968662 | ATTTTCCAAGCCCAG[-/T]TTTCCTTCTCAGTTT | 74164 |
| rs252989959 | in-del | -/TTGATTTTTT | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41000961 | ATGAGGCTGGATTGA[-/TTGATTTTTT]TTTTTTTTTTTTTTT | 74164 |
| rs253000548 | snp | C/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Nfx1 | Mm_Celera | 4:41011685 | AAAGGTCATGGAAAC[C/G]AGCTGAAGCCAGACA | 74164 |
| rs253026242 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41021466 | TCCAGGGCCAAGGAG[G/T]CAGGGATGGGGTCTT | 74164 |
| rs253027811 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41010973 | TGTGTAAGAGTGGGG[A/G]AATCAAGCTGAGCAG | 74164 |
| rs253136097 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41021108 | GTAATCGCAGTCAGC[A/G]ATAGGAGGATCACAG | 74164 |
| rs253241354 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40980756 | ATGCACATGCTCAGA[A/G]ATCAGAGGAGGATGG | 74164 |
| rs253300969 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40976048 | GTTATAGGTTCCCCT[A/G]CAGCTCAAGCTCTCC | 74164 |
| rs253310401 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40982424 | GGCTTACTACAGACA[C/T]ATATGGTTTTGAAAG | 74164 |
| rs253333668 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40975067 | TACAGTATACTCATA[C/T]ATAAAATGAATCTTA | 74164 |
| rs253336963 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40985396 | ACTGATGAAGTGGCT[A/G]CTGAAGGGGAAAGGG | 74164 |
| rs253415181 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40989038 | CTCCTGGCTCTAAGA[A/G]GAAAACTTATAGGCA | 74164 |
| rs253455479 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40996922 | ACAAAGGTAAGGCTA[A/G]AACTGTTTAACATGG | 74164 |
| rs253506315 | in-del | -/AAGAAGAAGAAGAAGAAGAAG | | | intron-variant | Nfx1 | Mm_Celera | 4:41023070 | AATAATAATAATAAT[-/AAGAAGAAGAAGAAGAAGAAG]AAGAAGAAGAAGAAG | 74164 |
| rs253604795 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41010224 | GGCCACTCAAAACCA[C/T]TTGTCACTCCAGTTC | 74164 |
| rs253616073 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40972729 | CTGGGACTGCGCTCT[A/T]GGTTACCACCGACAC | 74164 |
| rs253719558 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41016221 | TGTGCCTCCTCTCTG[A/C]TGCTAGAGACATGCT | 74164 |
| rs253722650 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41002039 | TCAAACTTGTGCTGG[A/T]CTTCTTGTCTTGGCC | 74164 |
| rs253723490 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41003430 | AGCTACAAGGGTGAG[A/G]TCTCTCTGGAACTGC | 74164 |
| rs253782028 | in-del | -/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41003803 | CGAATACCAAGTAAA[-/G]ATGTTGTAGATGGTG | 74164 |
| rs253787916 | in-del | -/ATATATAAAAAA | | | intron-variant | Nfx1 | Mm_Celera | 4:41020160 | TTTTTAAAAAAATAT[-/ATATATAAAAAA]ATATAGGTGTTTTTA | 74164 |
| rs253798566 | in-del | -/GGTCTC | | | intron-variant | Nfx1 | Mm_Celera | 4:41019105 | GCTGGCTGACTAGGA[-/GGTCTC]AAGCCTTCAGTCCAC | 74164 |
| rs253824568 | in-del | -/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40977362 | GTAAGTGTGCCTGGA[-/G]GGGGGAAGGCGGCAC | 74164 |
| rs253856578 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40978213 | TTGTTTTTTGTTTTT[G/T]TTTTTTTTTTTTCTG | 74164 |
| rs253901724 | in-del | -/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41006775 | TGGGGTCCTCTAGTC[-/T]TTTTTTTTTTAAGAT | 74164 |
| rs254010049 | snp | A/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969069 | AATAGACAACAGATA[A/T]AAAATGAGAAGTCTA | 74164 |
| rs254026334 | snp | C/G | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969654 | ATTCCTAAATGTGCT[C/G]GGTTAGGGGCAGGCT | 74164 |
| rs254059265 | snp | A/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969011 | GAGAAATATTTTTTT[A/T]AAAAGTCCATAGCAA | 74164 |
| rs254082902 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41008301 | AGTTCCCACCCAGCC[C/T]GTGTTCTACCACACG | 74164 |
| rs254085731 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40983919 | GAGAGTGCCAAGTAG[C/T]TAGGATTTCGGGCAT | 74164 |
| rs254100973 | in-del | -/AG | | | downstream-variant-500B | Nfx1 | Mm_Celera | 4:41026484 | CACTCAGGTCTGGGA[-/AG]AGTGTGTCTTTTGTC | 74164 |
| rs254108114 | in-del | -/CCTGTGC | | | intron-variant | Nfx1 | Mm_Celera | 4:40986052 | GCAGATGTTGCTGAT[-/CCTGTGC]CCTGTGCTGGGGCTT | 74164 |
| rs254112380 | in-del | -/ATGTCC | | | intron-variant | Nfx1 | Mm_Celera | 4:41010088 | GCAACTCCACAAGTG[-/ATGTCC]ATGTGTGTGGAACTC | 74164 |
| rs254135319 | snp | A/G | | | downstream-variant-500B | Nfx1 | Mm_Celera | 4:41026283 | AAGTCAACAGCTGTC[A/G]TCCAGGGTCTGAGAG | 74164 |
| rs254146560 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40984859 | GTGAGGGGTAGTTTC[A/T]TATGTTTCAGTTTGT | 74164 |
| rs254198789 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41017664 | CTGAGGTCTACCAAC[A/C]TCTGCCTCCCAAGGG | 74164 |
| rs254228383 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41003969 | CCTCTGGAATCTACA[C/T]GAATTCACACACGCA | 74164 |
| rs254240728 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40996055 | AGCTCACTCTCTCCA[A/G]CTTCATACTCAGAGA | 74164 |
| rs254285734 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40988144 | GCTCGTTGTGTGTGG[A/G]TTTCTGTCTGTTCAT | 74164 |
| rs254286609 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40996118 | CTAAAGGTGTGTGCC[A/C]TTCTACCTGGCTTGA | 74164 |
| rs254286774 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40996570 | CAGATAACTTTCAGA[A/G]CCTAGAGCATTTCAT | 74164 |
| rs254368129 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40974497 | TAAAGACGTTAACTC[A/G]TGCAAAGTGCTTAGG | 74164 |
| rs254405579 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41018657 | GGGTGGTGGGACACG[A/C]CTGTACTGTCAACCA | 74164 |
| rs254423177 | in-del | -/CATG | | | intron-variant | Nfx1 | Mm_Celera | 4:41004755 | ACACATCTAGGCATA[-/CATG]TTATTATATTCATGT | 74164 |
| rs254447654 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Nfx1 | Mm_Celera | 4:40970789 | GGGGGCAGTAGATCC[C/T]GCGGTCCGGGTGGGT | 74164 |
| rs254449421 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40988834 | GGGGAAAGAGTGATA[C/T]CAACCATTTGTTGAG | 74164 |
| rs254488904 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41022134 | ACAGCTCCTGGTCTG[G/T]CAACTCCTCTCTTCT | 74164 |
| rs254513828 | in-del | -/TC | | | intron-variant | Nfx1 | Mm_Celera | 4:40977505 | CAATTGGTAATCTCT[-/TC]TCTCTCTCTCTCTTT | 74164 |
| rs254635295 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41022652 | GACTAAGCAGAGAAA[C/T]CCTGTCTCATGGGGA | 74164 |
| rs254643988 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41009792 | AAAGAGCTGGTGAGC[G/T]TCTGAATTACTGAGC | 74164 |
| rs254659362 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41014737 | AAAAAAGAAAGCCAG[C/G]CACAATGGTGTGCAC | 74164 |
| rs254661895 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41006415 | TAATGTACATAAAAT[A/G]TAATACCAATTTGTA | 74164 |
| rs254787130 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41022200 | GTGGGCAGAAGGGGG[A/T]GGAAGAGGTTCCCAG | 74164 |
| rs254806846 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40997936 | ACAACTGATTCCTAG[A/G]TTATTTGGAAGATGT | 74164 |
| rs254877864 | in-del | -/GTC | | | intron-variant | Nfx1 | Mm_Celera | 4:40982037 | GATAGGAAAGCAGTG[-/GTC]GTCCATCATGGCTTC | 74164 |
| rs254969161 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40972815 | ATAGTCTTTGTTCTT[A/T]CTTTAACATCATTTC | 74164 |
| rs255017978 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41003837 | GAATCTTAGTGCTGG[A/G]GAGACAAAGACAGGA | 74164 |
| rs255059700 | in-del | -/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41024292 | TGGGCTGCAGGGGGC[-/G]GAGGCGGGGGGTAGA | 74164 |
| rs255158507 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41015014 | TTTTCTAAAGAGTCT[A/C]AGGTCTAGGAACGTA | 74164 |
| rs255212136 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40988498 | TTGTTTCAGAATGTA[C/T]GATAACATGGGTGTT | 74164 |
| rs255212748 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40977693 | CTCCTGCCTCAGCAT[C/T]CTGAGTAGCTTGTAC | 74164 |
| rs255219438 | in-del | -/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41016745 | ATAAATAAATATCTA[-/T]AAAAAAAAAATTTAA | 74164 |
| rs255327860 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40991148 | TGTTGTGCTTCTGGT[C/G]TGAGTTAACAGATCT | 74164 |
| rs255337980 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40980784 | TGGCAGATTGATCCC[C/G]CTCTTCTGTCCTCCT | 74164 |
| rs255338658 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41010931 | GGAGAGCTGACACTT[A/G]ATAGGTGTGAGGAAA | 74164 |
| rs255374816 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40980206 | TAAAAGTGTGTGCCA[C/T]CATGCCTAACTTTCA | 74164 |
| rs255376100 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40989257 | ATACAAATCACAGAC[A/T]GACACTTGTAAGCTG | 74164 |
| rs255453787 | in-del | -/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41003693 | TTAAATGCAGATTCT[-/C]CCATCTATTGCCTGA | 74164 |
| rs255475620 | in-del | -/TCTG | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40992373 | AAGGACTGATTGTTC[-/TCTG]TCTGTATGAATTCAT | 74164 |
| rs255485473 | snp | C/T | | | utr-variant-3-prime, intron-variant | Nfx1 | Mm_Celera | 4:41013539 | GAGGAAGGTTGGGAG[C/T]TTGAGGCCAGCCTGG | 74164 |
| rs255536974 | in-del | -/ACACACAT | | | intron-variant | Nfx1 | Mm_Celera | 4:41005665 | CACGTACATGCACAC[-/ACACACAT]ACACACACACACACT | 74164 |
| rs255605522 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41007111 | GCTGAAACCCTTTAC[A/G]TCAGTTCCTTGTGTT | 74164 |
| rs255646772 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41014557 | GGACATTTGGACTTT[A/T]AAAGTCTTAACTGTT | 74164 |
| rs255664562 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40992707 | CTCTTAACCATTGTG[-/CA]CTCTCTCTCTCTCCA | 74164 |
| rs255701430 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41017362 | TGTCACAAGCACGTG[C/G]TTTCTGACTGTTCTG | 74164 |
| rs255811048 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41002005 | GCCTACAGTTCACTA[G/T]TTGTAACCCATGCTA | 74164 |
| rs255846413 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41001458 | ACGCCAAAATGACTG[C/T]TTTATTCCAAAAGGA | 74164 |
| rs255872767 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40994280 | AGAGGATCCAGGTTC[A/T]ATTTTAAACACCAAC | 74164 |
| rs255908681 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41006132 | ATTTTGTGTGTGTGT[A/G]TTTTATGTATATTCC | 74164 |
| rs256014292 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40973386 | ACACACCAGAAGAGG[A/G]CGTCAGATCTCATTA | 74164 |
| rs256021523 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40994776 | CTCCCCATAGGTGGG[A/G]ATGACGCCTCTGAGC | 74164 |
| rs256053872 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40972635 | TCGTTTTCTCCTCCT[C/T]GCCCTGACTTATTTC | 74164 |
| rs256116145 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40985223 | AAAAAAAAGAAAAAA[A/G]AAAAGAAAATGTCTT | 74164 |
| rs256148467 | in-del | -/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41002743 | CTGCATAGGCAACCT[-/G]GGTGCTTCTCCAGGG | 74164 |
| rs256219657 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41019900 | TTATGTGTCTGTGTG[A/G]ATGTATGTCTCACAT | 74164 |
| rs256223140 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40972268 | GAGGTTTCTTTTACT[A/C]TCAACAACATACTCT | 74164 |
| rs256261687 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40981855 | TCTTCTAGAGGACTC[A/G]GGTTCTGTTTCCCAG | 74164 |
| rs256284210 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41020518 | ATAGCTCCAGAGTAG[G/T]AGTGCTTTTTCATTG | 74164 |
| rs256304980 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40992750 | TTATTTTTAAAATGT[-/AA]AAAAAAAAATATTTT | 74164 |
| rs256317526 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41008271 | GTAGTCACACCAGCA[A/T]GAAGTGCCCAGGCCA | 74164 |
| rs256341755 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41000202 | AGAGCCAGATGTGGT[A/T]TATCTCCACCATCCT | 74164 |
| rs256436704 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41008145 | TAAGAAAAAAATACT[G/T]GTTTTTTGAGACAGG | 74164 |
| rs256468316 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41010095 | CACAAGTGATGTCCA[C/T]GTGTGTGGAACTCTT | 74164 |
| rs256511617 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40999340 | ATTGTCCTGGTCCTG[C/G]TCCCCAAGTGCAGGC | 74164 |
| rs256514998 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41019390 | TCTACCAAACTGTAT[G/T]TCACTTCCTCTAGCA | 74164 |
| rs256539809 | in-del | -/A | | | intron-variant | Nfx1 | Mm_Celera | 4:40984520 | TTGTAGAAAACTCTT[-/A]AAGTCTATTCAGTGC | 74164 |
| rs256542507 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40991703 | GCTTCAGTCTGTGTA[A/G]TGGGAACTTCGGAGT | 74164 |
| rs256605138 | snp | A/T | | | utr-variant-3-prime | Nfx1 | Mm_Celera | 4:41025676 | AGTTTACGCCAAGCA[A/T]CCTACTGTAGGCCTT | 74164 |
| rs256621143 | in-del | -/TA | | | intron-variant | Nfx1 | Mm_Celera | 4:41010836 | TAACACAACTGATTT[-/TA]TATATATATATATAT | 74164 |
| rs256649125 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41000635 | AAGCACAAATCTTTA[A/T]AAAATAAATAAATAA | 74164 |
| rs256887486 | in-del | -/TC | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969538 | CACTCCCTCCTCTTG[-/TC]TCTCTCTCATCATCA | 74164 |
| rs256905912 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40989690 | CATGCTATAGCCCTG[A/G]CTACCTTCAGCCACT | 74164 |
| rs256925437 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40998621 | GGACTAAAGACATGT[A/G]CTACCATGTCTGACT | 74164 |
| rs256935679 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40982124 | TAAAATAACCCATTT[C/T]CTCCCCAGGTTGCTT | 74164 |
| rs256941561 | in-del | -/AAAAAAAAAAAAAAAAAAG | | | intron-variant | Nfx1 | Mm_Celera | 4:40971778 | CAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAAAG]GAACGTTTTGCATGG | 74164 |
| rs256958764 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40997834 | TCATTTCAGTTCATG[G/T]CAGGACTTCCTCTAA | 74164 |
| rs256972349 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40981055 | CTCGTGCAGGGTAGG[C/T]AAGCACTTTCCCTAC | 74164 |
| rs257079339 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40990636 | CAGGACAATCTGATG[A/G]CTGCAATCCTCTTCC | 74164 |
| rs257119759 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40982931 | GTCTTAGTATTGTGG[C/G]TGCCCACTATGTCCA | 74164 |
| rs257130124 | in-del | -/CCAA | | | intron-variant | Nfx1 | Mm_Celera | 4:41014925 | GCCAGAGAACCAACT[-/CCAA]CCAAACTGTTCTTGG | 74164 |
| rs257138403 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41000421 | GACTCAGCATGCAGT[A/C]ATGAGAACAAGAGTT | 74164 |
| rs257153994 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40991096 | TTAACTATTACGGCT[A/T]TATGCAGTATGAACG | 74164 |
| rs257191074 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41015929 | CCTCAGTTTACTTGT[A/G]TGGTGGTTAGCAGCT | 74164 |
| rs257211865 | in-del | -/CCCCCC | | | intron-variant | Nfx1 | Mm_Celera | 4:41021589 | CCTCTGCCCTCCACA[-/CCCCCC]CCCCCGTGTGCTCCT | 74164 |
| rs257234041 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41014817 | CCGGCCTTGACTATT[A/G]CAGATACTGTTTCAA | 74164 |
| rs257240103 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41014612 | TTAATCCCAACACTC[A/G]GGAGACAGAGACAGG | 74164 |
| rs257272831 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41008174 | GGGTTTCTCTGTGTA[A/G]CCCTGGCTGTCCTGG | 74164 |
| rs257466795 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40979581 | CCTCTGGATGCTGGG[A/T]TAGAGACATGGGACA | 74164 |
| rs257491906 | snp | A/G | | | upstream-variant-2KB | Nfx1 | Mm_Celera | 4:40970543 | GCCTCCCAGGTCCTG[A/G]AGTCGTGGGCTACCT | 74164 |
| rs257524735 | in-del | -/AAG | | | intron-variant | Nfx1 | Mm_Celera | 4:41021354 | AATAGTTTTTTTAAA[-/AAG]TAGCTAGCTAAGTTG | 74164 |
| rs257526312 | snp | A/G | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40970024 | AAGTGGTTTATTGGG[A/G]GAAGAGGAGTGAGGG | 74164 |
| rs257592446 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40991057 | CTAGAACAAGCTAGA[A/G]TCAGAGTCCTGTCTC | 74164 |
| rs257655508 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40982876 | TATTGCCAGTGAGAT[A/G]GTTTTATTTCTCTAG | 74164 |
| rs257705621 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41006359 | TCCTTCTGCCTCTGT[C/G]TCGGTTGCTGAGGTT | 74164 |
| rs257726375 | in-del | -/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41008625 | GCAGCATCTAAGTCC[-/T]TTTCCAAACAGTGTT | 74164 |
| rs257738876 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41005227 | TGTACTGGGGCATAT[A/G]ATCTCCACAAAACCA | 74164 |
| rs257867223 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41016888 | AACTTCAGAGTCCAG[C/T]GCCCCCTGTGGCCTC | 74164 |
| rs257944127 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40992506 | TGAAGACAGAATGTA[-/T]TTTTTTAATGTGTAT | 74164 |
| rs257945113 | in-del | -/CCACCCATCT | | | intron-variant | Nfx1 | Mm_Celera | 4:41018232 | CCTATATCCGGGAGG[-/CCACCCATCT]CCCTTGAGGAGGACC | 74164 |
| rs257966463 | in-del | -/GA | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Nfx1 | Mm_Celera | 4:41011776 | GCTTCAGTAGCAATG[-/GA]GAGAGACCCCACAGT | 74164 |
| rs258049428 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41009836 | GCAGCATCTTAATCT[A/G]ATTACAGCCCAGAGA | 74164 |
| rs258198723 | in-del | -/TTATT | | | intron-variant | Nfx1 | Mm_Celera | 4:40985803 | TCTTCAAGGCTACAG[-/TTATT]TTTTTTTTTTTTAAG | 74164 |
| rs258222261 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41024390 | GCGGCGATGGCAGCA[C/T]TGCCCGAGCAAATGC | 74164 |
| rs258247506 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41019993 | ACCTGAGCATCTCCC[A/T]AGCTCCAGTACTCCT | 74164 |
| rs258253634 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40978026 | TGTTGAGGATCACCC[A/G]TGGTCTCCAGCTTCT | 74164 |
| rs258373241 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40998325 | ATTCACGCTGTCCTC[A/G]CGCTCACAACCCATG | 74164 |
| rs258422692 | snp | A/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40968962 | CATGTACATACATAC[A/T]CTCAGACAATCATGT | 74164 |
| rs258429422 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40990344 | GAGCACTGTTGGCTC[A/C]CTCTTTTCCTTCTTT | 74164 |
| rs258431371 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40996169 | TAGTAAAATTAATAT[A/G]AGCGCGACACTGATG | 74164 |
| rs258488334 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41011040 | TTGCTCTCAGCTTTG[C/G]TCAGCTACTGAGCTC | 74164 |
| rs258490764 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41003149 | CATTCATTTGGAAGC[C/T]TCAGCCCTCTGGAAT | 74164 |
| rs258530044 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41010670 | GAGTCAGTGCTGGTA[A/T]CCGCTGAGCCATCTC | 74164 |
| rs258641895 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40974488 | TAAACAGAATAAAGA[A/C]GTTAACTCATGCAAA | 74164 |
| rs258642661 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40988322 | CCACAGATACTTGTC[A/C]GTTTAAGAAGATTTG | 74164 |
| rs258655648 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41024326 | ACAAAGTGGGATGCA[A/G]GTTGGCCACACTTGA | 74164 |
| rs258793975 | in-del | -/TTT | | | intron-variant | Nfx1 | Mm_Celera | 4:40994487 | AATTTGGATAGATAC[-/TTT]TTTTTTTTCTTTTAC | 74164 |
| rs258800228 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41000086 | CCCACCGGCATTATA[C/T]GCCTATATTGTCACC | 74164 |
| rs258889945 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41001610 | TTTATTTCATTTATC[A/T]TTTTTTTTTGAAGTT | 74164 |
| rs258953157 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40991723 | AACTTCGGAGTGATG[C/T]ATTTGTGTCTATCTT | 74164 |
| rs259092129 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40977395 | GGGACTCATTTTTAA[A/G]CAATACAGTTGCACA | 74164 |
| rs259135628 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40992729 | CTCTCTCCAGCACTA[A/G]AATGTTTATTTTTAA | 74164 |
| rs259210187 | in-del | -/C | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Nfx1 | Mm_Celera | 4:41011783 | AGCAATGGAGAGAGA[-/C]CCCCACAGTCCTGGA | 74164 |
| rs259231349 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40985145 | ATCTCTGAGTTTGGG[A/G]ACAGCCTGGTCTCTA | 74164 |
| rs259275040 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41019713 | TTGGAACTGGAGTTG[C/T]GGGTGATTGTGAGCC | 74164 |
| rs259306871 | snp | C/T | | | missense | Nfx1 | Mm_Celera | 4:41017977 | TAAATTTCAGAATAG[C/T]TGCTATTTCTATGGC | 74164 |
| rs259320516 | in-del | -/A | | | intron-variant | Nfx1 | Mm_Celera | 4:40999361 | AAGTGCAGGCTTTAC[-/A]GGTGTGTAGCATGCT | 74164 |
| rs259367910 | in-del | -/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40970331 | CACTCTCCCCCCCCC[-/T]CCAAAAAAAAAAAAA | 74164 |
| rs259386028 | in-del | -/A | | | utr-variant-3-prime, intron-variant | Nfx1 | Mm_Celera | 4:41013766 | TTTTACCCCCCCCCC[-/A]AAAAAGTCATCTTTG | 74164 |
| rs259428558 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41009954 | GTGTCCCGGCCCCCA[A/G]CACAAAGTTTTTTAA | 74164 |
| rs259429717 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40983137 | CTGCCTTAGCATCCT[A/G]GGATTTCAGGAATGC | 74164 |
| rs259456438 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40974292 | ATAGATGCTCAGCTG[C/T]TAAGAGCACTGTCTG | 74164 |
| rs259492259 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40973659 | ATTGACCGTGGCTTC[C/T]CTGGAAGGGCAGCCA | 74164 |
| rs259492305 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40984242 | ACGAACTGCAACTGG[A/T]CTATAAAACAGTTGT | 74164 |
| rs259492316 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41010541 | TATTTATTTAATTTA[C/T]TTATATGAGTATACC | 74164 |
| rs259557009 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40995323 | GAGACAGGATCTTGT[A/C]TGTAGCTCAGGCTGG | 74164 |
| rs259601087 | in-del | -/TCCTCCTCT | | | intron-variant | Nfx1 | Mm_Celera | 4:41019541 | TCTTCCTCCTCCTCC[-/TCCTCCTCT]TCCTCCTCCTCTAGC | 74164 |
| rs259604950 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40987785 | TGTTAGTCCCTTCTC[A/G]CTTTAGCTTCTCTTT | 74164 |
| rs259634866 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40995495 | GCTGGGCTGAGGTTG[C/T]AGCTCAGTTAGTAGA | 74164 |
| rs259673848 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41009584 | CACATACATGCCATA[C/G]CAGACTTGCATGCAC | 74164 |
| rs259710420 | in-del | -/AGA | | | intron-variant | Nfx1 | Mm_Celera | 4:40978555 | GTGCCCATGGAGGCC[-/AGA]AGAAGGAGTCAGACC | 74164 |
| rs259711298 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41008621 | AGTGGCAGCATCTAA[A/G]TCCTTTTCCAAACAG | 74164 |
| rs259740405 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41001314 | AGAGCAGTGTTGAGG[A/G]TGGTTCTGAAAGTAA | 74164 |
| rs259773002 | snp | A/G | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40970198 | GGGGCGTCTCTTTAG[A/G]CGCAGCACACACCTA | 74164 |
| rs259875079 | in-del | -/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41002790 | AGATATATATGCACT[-/C]CCATCTACAGAATAT | 74164 |
| rs259922606 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41001920 | TTAAACAAGCTTTTA[C/T]TTAAATGTGTTTTAA | 74164 |
| rs260047979 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40974106 | GCTGCCTTGCCTCTG[C/T]CAGGGTGCAGTGTGA | 74164 |
| rs260108603 | in-del | -/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41002105 | CAACACCCAATACTG[-/T]TTTTTGTTCTTTTTT | 74164 |
| rs260168626 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41005859 | CAAAAATGTAAGCCA[C/T]ACGATCGGTGTTGTG | 74164 |
| rs260171428 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40975864 | AGACTTTAAACCCAT[C/T]TTAGCTCATTTCAAA | 74164 |
| rs260225029 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40989001 | TGGGTGTCAAAGCCA[A/G]TGATCCTTCTGTTGT | 74164 |
| rs260260695 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41009460 | AGAATGAATCAGCAG[C/T]GGGTAAAGAAACTTC | 74164 |
| rs260346318 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41024415 | AAATGCCGGGTTTCT[A/G]GCTCTGCTGTTTCTG | 74164 |
| rs260365775 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41010159 | GGAGAGATGGCTCAT[C/T]TGTTAGAAGCACTCG | 74164 |
| rs260381509 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40998834 | TCACTGTACTGCCCA[A/G]GCTAGCCTTGAATTC | 74164 |
| rs260414471 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41002553 | TTTCATACACAAAAG[C/G]TTTTTATTTTATTGA | 74164 |
| rs260443055 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41016995 | TGCTTTATGGTGCCT[C/T]TATGGGCTGGTGAGA | 74164 |
| rs260472211 | snp | A/T | | | utr-variant-3-prime | Nfx1 | Mm_Celera | 4:41025316 | TTAAACCTACCCATC[A/T]TATCCAAAAGCTCCC | 74164 |
| rs260517099 | in-del | -/TTG | | | intron-variant | Nfx1 | Mm_Celera | 4:41006205 | TTAAACTTGCTTTTT[-/TTG]TTGTTGTTATTATTA | 74164 |
| rs260518560 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40973657 | AAATTGACCGTGGCT[C/T]CCCTGGAAGGGCAGC | 74164 |
| rs260533671 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40978911 | GCATCAGATCCCCTG[A/G]AACTGAAGTTACAAG | 74164 |
| rs260535980 | snp | C/T | | | synonymous-codon | Nfx1 | Mm_Celera | 4:41024483 | CCACAGAGGGAAGTC[C/T]GTTTGTCCTCCTACC | 74164 |
| rs260576220 | in-del | -/A | | | intron-variant | Nfx1 | Mm_Celera | 4:41014982 | TACTAAATTCATGTC[-/A]AAACAACAGACAGCT | 74164 |
| rs260662257 | snp | C/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969506 | CAACTTGCCCACAAA[C/T]GTCTGTTCTCTCCCC | 74164 |
| rs260699547 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41010410 | AACCTGACAGCTTAA[A/G]CTCAGCCCCTGGATC | 74164 |
| rs260730097 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41019759 | AGAACTGAATCTAGG[C/T]TGTCTGCAAGAGCAA | 74164 |
| rs260824659 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41004461 | TTCACTCTGGACTTG[C/T]CTTTATTCCCAGCAC | 74164 |
| rs260869094 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40996242 | TGCACAGTTCCCTGA[C/G]CTTGGCTTTCAGTGC | 74164 |
| rs260942852 | in-del | -/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41018996 | TTAAGGCAGACTGAT[-/C]TTAAACTCCCAGAGA | 74164 |
| rs260984952 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40971271 | AGAGCGGGCGGGTCC[A/C]GGCGCCAAGGGAGCG | 74164 |
| rs260990818 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40987900 | ATTCTTGATTGAGTA[A/T]AATACTGGGAAGATA | 74164 |
| rs260994638 | in-del | -/CAC | | | intron-variant | Nfx1 | Mm_Celera | 4:40995574 | TCCACACACTCCACA[-/CAC]AAGTAGAGGCAGAGA | 74164 |
| rs261021214 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41022451 | GTTGCATATTTTCAG[C/T]ACCAAGCCATTATCA | 74164 |
| rs261040438 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40979307 | GATTACATACATGAC[A/G]GTGCGACTAGTCTTA | 74164 |
| rs261113483 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40971121 | GTCCGAAGGGTGCGG[A/G]CCATTGCGGTGGCAA | 74164 |
| rs261224564 | snp | C/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Nfx1 | Mm_Celera | 4:41011825 | TGCTGAGAGCTGCTG[C/G]TGTGGCGTCGATCCA | 74164 |
| rs261225064 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41018894 | TCTGTTCTTGTGCCT[C/T]TCCCACCCTAGTTCC | 74164 |
| rs261225618 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40979393 | GCCTCTGGGTTTAGG[A/G]ACTGAAGATATGTAC | 74164 |
| rs261252834 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40987953 | CACTGGGAAGTTGGG[C/T]AGACAGAAAATAGCA | 74164 |
| rs261254423 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40978242 | TGTTGGGTTTTTGTG[A/G]TTTTGCTTTTTTGGC | 74164 |
| rs261306996 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41020696 | CAGGGGAATCCTGCC[A/G]TACAATGTTTCAATG | 74164 |
| rs261326320 | in-del | -/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41002841 | TCTTACCATACCATG[-/T]ATTAATCAGCTTCAG | 74164 |
| rs261351646 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41009928 | CAGTGTCTTCTCTGT[A/C]CTGGTGAACCGTGTC | 74164 |
| rs261381335 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41007034 | TCTCTCCCACCCCCA[A/G]CATTGATTTTTAAAA | 74164 |
| rs261391579 | in-del | -/A | | | intron-variant | Nfx1 | Mm_Celera | 4:41014409 | ACCACCGTCATGCTT[-/A]ACAGCATTGTAAAAG | 74164 |
| rs261402831 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Nfx1 | Mm_Celera | 4:41011921 | GAGCCTGGAAGATAA[C/T]ATTATGATTGAGTTC | 74164 |
| rs261434834 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41021927 | GTATAGTAATCAGTT[A/G]TGTGTTTCCCCCATA | 74164 |
| rs261434909 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41011187 | CATAAATGAGTCTAG[A/G]ACAGAGGTCAGCACT | 74164 |
| rs261472151 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40986598 | TCCCTACCAATGAGC[C/T]ATATCCCTAATCCAG | 74164 |
| rs261504165 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40982643 | AATTAGAATCATACA[A/G]TAGACACAGTCGTGG | 74164 |
| rs261580021 | in-del | -/TAAAG | | | intron-variant | Nfx1 | Mm_Celera | 4:41016758 | CTAAAAAAAAAAATT[-/TAAAG]TAGAGTTTTACATCT | 74164 |
| rs261596047 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40978138 | GCTGGATGCAGTTCC[C/T]TCTATAGAGTGCCTA | 74164 |
| rs261625207 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40973042 | TCTATGCTCCCAAAG[A/G]CCTCACAACCCACAG | 74164 |
| rs261661853 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41011099 | ACCTGGAATTGTAAG[C/G]CAAACAGAAACCATT | 74164 |
| rs261688637 | in-del | -/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40988095 | ACCATGAAAGTGCAG[-/C]CCCTTTATGCCTCCT | 74164 |
| rs261689852 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41008466 | TAAAAAAATTCCCAT[C/T]ATGAGGTTCTCTTCA | 74164 |
| rs261745982 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41003935 | TATCTAAAGGAGGCA[A/G]AAAATATTATGAGTT | 74164 |
| rs261780018 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41000035 | AGGATAGTTGAGAAT[C/T]TGAAGCCTTGTCTCA | 74164 |
| rs261784405 | in-del | -/CCTAC | | | utr-variant-3-prime | Nfx1 | Mm_Celera | 4:41025306 | ATCGTGTGTCTTAAA[-/CCTAC]CCATCTTATCCAAAA | 74164 |
| rs261819793 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40980454 | TACTAAAGACCCTTC[C/T]CCTCGTAAGGATAAG | 74164 |
| rs261879586 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40996396 | GACTTTGAGGCCATC[C/T]TGGACTACATAATAA | 74164 |
| rs261899519 | snp | C/T | | | utr-variant-3-prime, intron-variant | Nfx1 | Mm_Celera | 4:41013304 | TCACACCCCTGCCTT[C/T]ATGGATCAATCGTTC | 74164 |
| rs261903705 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Nfx1 | Mm_Celera | 4:40970735 | AAAGGCGTAGCAGCT[A/G]GAGAACCCAGCAGCT | 74164 |
| rs261941520 | in-del | -/ACACACAC | | | intron-variant | Nfx1 | Mm_Celera | 4:41010491 | TGGCACATGTGCATT[-/ACACACAC]ACACACACACACGTC | 74164 |
| rs261960959 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41006389 | TACAAGCATACAGCA[G/T]CATATCTGTATAATG | 74164 |
| rs261971451 | in-del | -/AGAT | | | intron-variant | Nfx1 | Mm_Celera | 4:40982556 | GAAAAGTTTACAGTC[-/AGAT]AGCACTTCAGTTAGG | 74164 |
| rs261981458 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40990294 | TCACCAGCTGATGAG[A/G]ACAGTTCTGTGCTTC | 74164 |
| rs262075115 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40981720 | TTCTTTATAAATGTA[A/G]TTGATGTGGTGGGCC | 74164 |
| rs262130258 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41015642 | GCTAAGTGATGGCTC[A/G]GGTCATCAGGACCAT | 74164 |
| rs262134363 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40972738 | CGCTCTAGGTTACCA[C/T]CGACACGCCCCAAAG | 74164 |
| rs262153726 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40982425 | GCTTACTACAGACAT[A/T]TATGGTTTTGAAAGA | 74164 |
| rs262190238 | in-del | -/A | | | intron-variant | Nfx1 | Mm_Celera | 4:40979331 | AGTCTTAGACTAGTT[-/A]AAAAAGAAAATGCTT | 74164 |
| rs262200674 | in-del | -/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41007138 | TGTTGGGGTGACCCC[-/T]AACCAGAAATTATTC | 74164 |
| rs262248700 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40988106 | GCAGCCCCTTTATGC[C/T]TCCTGGGAAGCTTCG | 74164 |
| rs262267719 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40995950 | GGTCTATTACATACA[C/T]TGACATGTGTGCATA | 74164 |
| rs262303452 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40993517 | GACTGGATCGGGCCC[-/T]TCTGACGCCTGAGGT | 74164 |
| rs262309699 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40983849 | CCCTAAGTTGCCTAG[G/T]CTGGCTTCCCTATTA | 74164 |
| rs262332364 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40991427 | TGGTACGAGAGGCCA[A/G]TGAGATTGCTCAGTG | 74164 |
| rs262391917 | snp | A/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | Nfx1 | Mm_Celera | 4:41012235 | GTAACATGTTTGTGT[A/G]CTAAGTTGACATGGG | 74164 |
| rs262432368 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41017609 | TTGTAATTGTGACTT[A/G]CCAGAGCTCACTGCG | 74164 |
| rs262464720 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41009327 | TATAATTTAATTGCT[A/T]AAACATTGTTAGTCT | 74164 |
| rs262557188 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40981458 | TCAGACCCCTTGACT[A/G]TCCATCCCCCTTCTC | 74164 |
| rs262575111 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40989758 | TTGCAAGTGTGAGCC[A/G]CTTCATCCAGCAGAA | 74164 |
| rs262647699 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40976191 | ATACTAATCGTCCTT[C/T]ACAGGGACTGATAGT | 74164 |
| rs262666094 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40985588 | TTAGGCATTGTGGTG[C/T]GCATGGATAATCCCA | 74164 |
| rs262688350 | snp | C/T | | | synonymous-codon | Nfx1 | Mm_Celera | 4:41023634 | GAATAACAAGAAAAG[C/T]CACTGCTTCCCCCCC | 74164 |
| rs262719467 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41015027 | CTCAGGTCTAGGAAC[A/G]TAACTCAGTGCTACA | 74164 |
| rs262754892 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40991029 | GGGTAAGCCAGCAGA[A/G]TCAGGATACTTACTA | 74164 |
| rs262761038 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41008507 | GTGTAGATGGGCCAG[A/G]AAACAAGGAGGCAAG | 74164 |
| rs262779286 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40999097 | AGCAAATGGCATGTG[A/G]TAGGCCTTTGGGGCT | 74164 |
| rs262794609 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40991166 | AGTTAACAGATCTGG[A/G]CGCACATTGACTCCT | 74164 |
| rs262847157 | in-del | -/CTGCT | | | intron-variant | Nfx1 | Mm_Celera | 4:40972356 | ATTTGACATAATGGC[-/CTGCT]CTTCCTGAAAATCAC | 74164 |
| rs262895889 | in-del | -/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40987280 | TAGGTATATGTCTTC[-/T]TTTTTCCCCTTTTAG | 74164 |
| rs262935777 | in-del | -/GCCAGCCA | | | intron-variant | Nfx1 | Mm_Celera | 4:41003872 | CCTTGGAGCTTGCTT[-/GCCAGCCA]TTCTAACCTAATTGA | 74164 |
| rs262938183 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40985085 | CTGGGTGGAAACAGT[A/G]ATGCACACCTTTAAT | 74164 |
| rs262967921 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40975288 | AGACAGATGATTTAA[A/C]ACAATAAATAGTAGA | 74164 |
| rs263046481 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40971658 | CACTCTCCCTCCTGG[A/G]GCTACCCCTGTGGTA | 74164 |
| rs263078803 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41000684 | GAGATTGCTCAGCAG[G/T]ATTGGCTGCTCTTAG | 74164 |
| rs263115963 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41022766 | GTTGCCTGTGAGGGA[A/G]CACACTCTTATTTTC | 74164 |
| rs263197775 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40998835 | CACTGTACTGCCCAG[A/G]CTAGCCTTGAATTCA | 74164 |
| rs263218952 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41018743 | TCTTAGGCATCTGAG[A/G]CCAGACTGGGCTACC | 74164 |
| rs263332219 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40991616 | ATTAAAAATTTGAAG[A/G]AAACACTTAGAAAAA | 74164 |
| rs263390709 | snp | A/G | | | downstream-variant-500B | Nfx1 | Mm_Celera | 4:41026319 | TTTGTGCATGCAAGA[A/G]AGGGAACTCTGACTT | 74164 |
| rs263419545 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40994670 | TATAATAGGAACATG[C/T]AAAAACAACACTGGA | 74164 |
| rs263432333 | in-del | -/A | | | intron-variant | Nfx1 | Mm_Celera | 4:40991271 | GGTTCTCCTTCCTGC[-/A]TGCTGCTCAGTGAAC | 74164 |
| rs263443269 | in-del | -/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40974710 | TGTAGGGATTGTTCT[-/C]CATTACATATAAGAA | 74164 |
| rs263459591 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40986505 | GTACTTGGCCAGAGT[G/T]TCAGTCTTTTGTAAA | 74164 |
| rs263465991 | in-del | -/TG | | | intron-variant | Nfx1 | Mm_Celera | 4:40975159 | CATGATAGCACACAC[-/TG]TAATCATATCACTCA | 74164 |
| rs263468297 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41017777 | CATGTTAACTCTTCT[C/T]GTGCAGCTACTTAGA | 74164 |
| rs263546365 | snp | A/G | | | intron-variant, downstream-variant-500B | Nfx1, Mir3094 | Mm_Celera | 4:40993865 | ATGTGGCAAGTAAGG[A/G]TTTCCTTTTTTTACC | 74164 |
| rs263581928 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41020440 | ACACTGAATAAACTC[A/C]ACACAGGCATCTCAG | 74164 |
| rs263626789 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40985642 | CTAGCCCTGTCTACA[C/T]AACAGGTTTCATGAC | 74164 |
| rs263635675 | in-del | -/TT | | | intron-variant | Nfx1 | Mm_Celera | 4:41016741 | TAAAATAAATAAATA[-/TT]TCTAAAAAAAAAAAT | 74164 |
| rs263649923 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40974985 | CAAGCAGGGCTGACC[A/G]GAGCGAGCAGAGGTC | 74164 |
| rs263751318 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41019864 | GTCTCACATGTACAG[A/G]GAGATTTATTTCTAT | 74164 |
| rs263764084 | in-del | -/C | | | intron-variant | Nfx1 | Mm_Celera | 4:40971911 | ACAGAGCAGTCACGT[-/C]TCGCTTGCACAACCA | 74164 |
| rs263820112 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41001849 | ATAATCAAAGATGCA[C/T]TTGCAACAACCTGCA | 74164 |
| rs263874794 | in-del | -/TC | | | intron-variant | Nfx1 | Mm_Celera | 4:40985767 | TTTGCATTTCACAAA[-/TC]TCTGTAGTATTCTAG | 74164 |
| rs263890769 | in-del | -/TGTTTG | | | intron-variant | Nfx1 | Mm_Celera | 4:40989364 | TACTTTTTTGGGTAT[-/TGTTTG]TTTTTGTTTTTGTTG | 74164 |
| rs263906396 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41008304 | TCCCACCCAGCCTGT[G/T]TTCTACCACACGCAG | 74164 |
| rs263917805 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40977842 | AGGACCTGGTAACAA[A/G]CATATCAGTGCCTCT | 74164 |
| rs263940102 | in-del | -/CCCCC | | | intron-variant | Nfx1 | Mm_Celera | 4:40986672 | TTCATTCTCTCTTCT[-/CCCCC]CCCCCCTCCCCTCCA | 74164 |
| rs263998447 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41000935 | GAAAATGTTATAAGT[G/T]GTGGGTGCAAATGAG | 74164 |
| rs264081329 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41003585 | GGGTGACTTTTGCCC[C/T]GGCACAGACTGGTAT | 74164 |
| rs264175892 | snp | A/T | | | missense | Nfx1 | Mm_Celera | 4:40976691 | AAAGCACAAGGGCTC[A/T]CTGAGCAGACGTCAG | 74164 |
| rs264299506 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40994873 | GGTAAAACCGGCAGC[C/T]TCTCCAGGGCTGGGA | 74164 |
| rs264335589 | in-del | -/GAACT | | | intron-variant | Nfx1 | Mm_Celera | 4:41019745 | CCTTGCGGGTAAGGA[-/GAACT]GAATCTAGGCTGTCT | 74164 |
| rs264350175 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41023399 | GACAACTTTAGTTTC[A/G]TCCCAGGAACCCACA | 74164 |
| rs264380973 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40972019 | TGTCCCCCCAAAGCA[C/T]CCTTGCTAAAACAGG | 74164 |
| rs264469672 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41009694 | GTGTCCATGGAGCCC[A/G]GAAGAGGACATCAGA | 74164 |
| rs264477894 | snp | C/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969985 | CCTTGAGAAATTACG[C/T]CATGCAAACAAGACC | 74164 |
| rs264539467 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41005071 | CATGGTGCCTCCTCA[A/G]CAGTATGCTCATCTC | 74164 |
| rs264613344 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40996728 | GAGGGAAGCTGAGGA[C/T]GAGGACACAGCGTTG | 74164 |
| rs264640318 | snp | C/T | | | missense | Nfx1 | Mm_Celera | 4:40977285 | GATCCCCAAGTGCTA[C/T]CTCCTTTTCCCAGAG | 74164 |
| rs264650738 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40985989 | CCACTGAGCCATCTC[A/T]CCAGCCCCTCTAGGC | 74164 |
| rs264696364 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41010798 | GGCTTTGCACATGTT[A/T]AGTATACTGGTTAGT | 74164 |
| rs264704590 | in-del | -/ACA | | | intron-variant | Nfx1 | Mm_Celera | 4:41006416 | ATGTACATAAAATGT[-/ACA]AATACCAATTTGTAT | 74164 |
| rs264749036 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41004989 | GCCTACTCATACCTT[A/G]TCATTCAGAATGTTG | 74164 |
| rs264840474 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40980952 | GGAGGATGGCCTTAA[A/G]CTATTGGTCCTCTTG | 74164 |
| rs264856960 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40971537 | AGGGGGTGTGAAATC[C/G]CATATTGAGGTGCGT | 74164 |
| rs264899523 | in-del | -/CTTCGAG | | | intron-variant | Nfx1 | Mm_Celera | 4:40994829 | TTTTCTAAACTTTTC[-/CTTCGAG]CAGGCTCTAACTAAG | 74164 |
| rs264912174 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41007275 | CCATCTACTTCCCCC[A/C]AAAAGAGGCAACAAC | 74164 |
| rs264975008 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40995002 | CCTGTTACCCTGACT[A/G]AAGTGATGATGTGGG | 74164 |
| rs265040709 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40992841 | ATTTTATGGATATGA[-/T]TTTTTTTAAAACTAT | 74164 |
| rs265082030 | snp | G/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41022608 | TTCAAGGTCAGCCTG[G/T]TCTACAGAGTGAGTT | 74164 |
| rs265090916 | in-del | -/TTGCT | | | intron-variant | Nfx1 | Mm_Celera | 4:40990770 | CTACCTCATTGAAGC[-/TTGCT]TTTTTTTTTTTCTTT | 74164 |
| rs265125171 | snp | A/G | | | utr-variant-3-prime, intron-variant | Nfx1 | Mm_Celera | 4:41013706 | TTGGGGAAGTGTAAG[A/G]AGGAGGATCAGGAGT | 74164 |
| rs265167171 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40990421 | CAGGGTCTCCCACAT[A/G]TCAGTAAGTGCTCTT | 74164 |
| rs265210558 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40982300 | TAGAGAAGAGTGGCT[A/G]TAGGGAGCACAGCCA | 74164 |
| rs265243473 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41016177 | AGAAATGCTCAAAAA[A/C]CGGGTGGCCTTGGTG | 74164 |
| rs265330532 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40984431 | CTGGGTGTGGTAACA[C/G]TCAAGAAATGGAGAC | 74164 |
| rs265462276 | in-del | -/TA | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40968777 | ATCATCTTTCTGGTG[-/TA]TATATATATATACGT | 74164 |
| rs265463004 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41023588 | CCAGGGCATGGAAAT[A/G]ATCAGTCTTCTCTCC | 74164 |
| rs265478485 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40972529 | CCCAGTCTTGACTTG[A/G]ATGTAAAAATCTTCT | 74164 |
| rs265556519 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40999429 | GGTCAGGAAATCATG[C/T]TTGATACCTTTAGAC | 74164 |
| rs265570653 | in-del | -/TTG | | | intron-variant | Nfx1 | Mm_Celera | 4:41024724 | GGGCATCAGACACAC[-/TTG]TTGAAGCCTTAATTC | 74164 |
| rs265620254 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41017173 | CCGTACATACATCAT[A/G]CATACACAGTAATAA | 74164 |
| rs265704158 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40985179 | TGAGTTGCGGGACAG[C/T]CAGAGCTACACAGAC | 74164 |
| rs265714135 | snp | A/T | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | Mm_Celera | 4:40992842 | ATTTTATGGATATGA[A/T]TTTTTTAAAACTATT | 74164 |
| rs265786177 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:41019261 | GGGATCATAGGTGTA[C/T]GCCACCATGCGTAGG | 74164 |
| rs265850295 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40973477 | GTCAGTGCTCTTAAC[C/T]ATTGAGCCATCTCTC | 74164 |
| rs265857229 | in-del | -/CTGTATG | | | intron-variant | Nfx1 | Mm_Celera | 4:41009674 | TGCCTGCACATATAT[-/CTGTATG]CCTGGTGTCCATGGA | 74164 |
| rs265880519 | snp | C/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41008587 | ATACTTAACTCGCAT[C/G]GATGGCAAGAAAACA | 74164 |
| rs265923451 | snp | A/C | | | intron-variant | Nfx1 | Mm_Celera | 4:41000264 | AAGGGACGGCTCAGT[A/C]GAGAGTCTCTTAAAG | 74164 |
| rs265962033 | snp | C/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40975389 | TTCCTCCCTCCCTCC[C/T]GCCTTCTCTTTCTCA | 74164 |
| rs266027102 | in-del | -/TCCTCC | | | intron-variant | Nfx1 | Mm_Celera | 4:41019529 | GCTCGGTAACTCTCT[-/TCCTCC]TCCTCCTCCTCCTCC | 74164 |
| rs266039842 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41002098 | TAAAATACAACACCC[A/G]ATACTGTTTTTTGTT | 74164 |
| rs266082011 | snp | A/T | | | intron-variant | Nfx1 | Mm_Celera | 4:40994386 | GATTTTATTTTTTTA[A/T]AAATGTAAATGTTTA | 74164 |
| rs266116363 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40995800 | CACTGGGTTAAAAAG[A/G]AGAGAACTGACTCAG | 74164 |
| rs266123805 | snp | A/G | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969132 | TTCAACCAGAAGGCT[A/G]ACAAGGAGTCAGCAG | 74164 |
| rs266157466 | snp | C/T | | | upstream-variant-2KB | Nfx1 | Mm_Celera | 4:40970442 | TATTAGTCCTTTAGA[C/T]ACTGTGTTTCGTTTT | 74164 |
| rs266187195 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41003970 | CTCTGGAATCTACAC[A/G]AATTCACACACGCAC | 74164 |
| rs266237112 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:40997448 | TGTCATCCTGGTATG[A/G]CCTACAAAGCCAATG | 74164 |
| rs266249529 | snp | A/G | | | intron-variant | Nfx1 | Mm_Celera | 4:41006219 | TTTGTTGTTGTTATT[A/G]TTATCTTTACATGTG | 74164 |
| rs387582687 | in-del | -/GT | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40968833 | TGTGTGTGTGTGTGT[-/GT]TTGTGTGAGAGAGAC | 74164 |
| rs578283843 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40981602 | CTGTCCTGTCCTGGA[A/G]CTCACTCTGGTAGAC | 74164 |
| rs578286707 | snp | C/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41013974 | TGTGTGATGGGAGAA[C/G]GTGAGTGTCACAGTG | 74164 |
| rs578295226 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41023118 | GAAGAAGAAGAAGAA[G/T]AAGAAGAAGAAGCCA | 74164 |
| rs578658843 | snp | A/C | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41023125 | AAGAAGAAGAAGAAG[A/C]AGAAGCCAGTACAGC | 74164 |
| rs578684928 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40995669 | CCATGTCTCTAAAAA[C/T]GGAAAGTTTTTTTTC | 74164 |
| rs578770470 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41019855 | TGGATGTATGTCTCA[C/T]ATGTACAGGGAGATT | 74164 |
| rs578771253 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41005185 | TCCCAACCCACCCAC[C/T]CCCACTTCCTGACCC | 74164 |
| rs578786307 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40990095 | TTTTTTTTCCTTGTT[C/T]TAGCTTCTCTCCAAC | 74164 |
| rs578819651 | snp | A/C/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40971376 | CGGGCGGGCGGGCGG[A/C/G]CGGCCGGCCGGCCGG | 74164 |
| rs578866458 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41005215 | CTGGCATTCCCCTGT[A/G]CTGGGGCATATAATC | 74164 |
| rs579249732 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41005652 | CACATGCATGTGCAC[A/G]CGTACATGCACACAC | 74164 |
| rs579267319 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40973508 | TAGTCCCCTCCTCAA[A/G]TCTCTTTATAGATCT | 74164 |
| rs579279662 | snp | A/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40989255 | GAATACAAATCACAG[A/T]CAGACACTTGTAAGC | 74164 |
| rs579319527 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41000961 | ATGAGGCTGGATTGA[G/T]TGATTTTTTTTTTTT | 74164 |
| rs579358980 | snp | C/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | Nfx1 | GRCm38.p3 | 4:41012296 | ACAACCTAGAGTCAC[C/G]CAGAGTCTTAGTGAG | 74164 |
| rs579361341 | snp | A/G | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969547 | CCTCTTGTCTCTCTC[A/G]TCATCATCATCTCAC | 74164 |
| rs579371445 | snp | A/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40980697 | TTGTGTGTGGTGTGT[A/T]TGTGTATTGTGTGTG | 74164 |
| rs579440706 | snp | A/G | | | utr-variant-3-prime | Nfx1 | GRCm38.p3 | 4:41025579 | GTTGCTTTTTTCCTA[A/G]GCTTTCAGCAGCCAT | 74164 |
| rs579442434 | snp | A/G | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969556 | TCTCTCATCATCATC[A/G]TCTCACTACTGCAGG | 74164 |
| rs579655203 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40985901 | CAGATCTCATTACGG[A/G]TGGTTGTGAGCCACC | 74164 |
| rs579690758 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41016692 | GATGCCCTCTTCTGG[C/T]GTGTCTGAGGACAGC | 74164 |
| rs579771717 | snp | C/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969772 | TGTTTGAGACAGTGT[C/T]GTACTGTTGCTCTGG | 74164 |
| rs579789048 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41003302 | ACATACATATAGGAA[A/G]ACAGAGAAGGCCTCC | 74164 |
| rs579838206 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41014934 | ACCAACTCCAAACTG[C/T]TCTTGGACCTCTTCA | 74164 |
| rs579909419 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40974830 | TGGCTCACAACCATC[C/T]ATAATGAGATCTGAT | 74164 |
| rs579958532 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40991218 | AGGACAGGCAGCTGG[C/T]AGAGGAGGACAAGTG | 74164 |
| rs579995651 | snp | A/C | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40991394 | GAGGCAGTGAGGAGA[A/C]TATTGAAATTAAAAA | 74164 |
| rs580007618 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41020303 | AGTCCTGCAAGAGCA[A/G]CAGTGCTTCAGCTGC | 74164 |
| rs580032130 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40974845 | CATAATGAGATCTGA[C/T]GCCCGCTTCTGGAGT | 74164 |
| rs580238994 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41019783 | AGAGCAACAAGTGAC[G/T]TAACCATCTCTCCTG | 74164 |
| rs580321060 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41007589 | GAATCAATCAATGAC[C/T]TTTATTGGTGTTATT | 74164 |
| rs580321948 | snp | A/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41021351 | ATAAATAGTTTTTTT[A/T]AAAAGTAGCTAGCTA | 74164 |
| rs580526207 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41016353 | ATTTATTTATTTATT[A/G]CCTGTGTGTGTGTGT | 74164 |
| rs580573514 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40989934 | GTGTGTGTGCACTCG[C/T]GTGTGCAAACACAAA | 74164 |
| rs580873960 | snp | C/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40972430 | TGACAGATTGATGGG[C/G]CACTATTAGGATGTG | 74164 |
| rs580890289 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41004178 | GGGAGTGCTCTGCTC[A/G]GTCTCGGGGTCCCTG | 74164 |
| rs580904342 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40971364 | GAGTCCGGCGGGCGG[A/G]CGGGCGGGCGGACGG | 74164 |
| rs580937591 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41005197 | CACTCCCACTTCCTG[A/G]CCCTGGCATTCCCCT | 74164 |
| rs580978868 | snp | C/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41010388 | TAGTGCGTAAAGGTG[C/G]GTGACAAACCTGACA | 74164 |
| rs581042085 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40977517 | CTCTTCTCTCTCTCT[C/T]TTTTTCTTCTTGGTT | 74164 |
| rs581048464 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41018227 | TGACTCCCTATATCC[A/G]GGAGGCCCTTGAGGA | 74164 |
| rs581062862 | snp | A/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40986094 | TAACAGCATGTGTCT[A/T]CTCAAGTCAGTCTCC | 74164 |
| rs581072281 | snp | C/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40995539 | TGAGTGAAGCTACTG[C/G]TTCCATCCTCAGCTA | 74164 |
| rs581075732 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41023121 | GAAGAAGAAGAAGAA[G/T]AAGAAGAAGCCAGTA | 74164 |
| rs581350092 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | GRCm38.p3 | 4:40992855 | GATTTTTTTAAAACT[A/G]TTCTCACTATATAGC | 74164 |
| rs581435989 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41023061 | TAATAATAATAATAA[G/T]AATAATAATAAGAAG | 74164 |
| rs581531435 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41019269 | AGGTGTACGCCACCA[C/T]GCGTAGGTTCCACTT | 74164 |
| rs581534329 | snp | A/C | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Nfx1 | GRCm38.p3 | 4:41011790 | GGAGAGAGACCCCAC[A/C]GTCCTGGAGATGCCA | 74164 |
| rs581546806 | snp | A/C | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40980681 | CACCCGCATGCTACC[A/C]TTGTGTGTGGTGTGT | 74164 |
| rs581589856 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | GRCm38.p3 | 4:40993163 | CTCGAACTCAGAAAT[C/T]CGCCTGCCTCTGCCT | 74164 |
| rs581620012 | snp | A/C | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40986679 | TCTCTTCTCCCCCCC[A/C]CCCTCCCCTCCAGAT | 74164 |
| rs581702945 | snp | C/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40970199 | GGGCGTCTCTTTAGA[C/T]GCAGCACACACCTAT | 74164 |
| rs581705127 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41003405 | ACACATGAGTGCAGG[G/T]GTCTGCAGAAGCTAC | 74164 |
| rs581995484 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41019802 | CCATCTCTCCTGATT[C/T]TTTAGAGATTTATTT | 74164 |
| rs582004405 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40973519 | TCAAGTCTCTTTATA[A/G]ATCTTTCTTTTTAAA | 74164 |
| rs582088170 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41005654 | CATGCATGTGCACAC[A/G]TACATGCACACACAC | 74164 |
| rs582164045 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41019890 | TCTATTGTGTTTATG[C/T]GTCTGTGTGAATGTA | 74164 |
| rs582170497 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40991192 | CTCCTTTCTTTCCTG[A/G]CTGGTAGAGGAGGAC | 74164 |
| rs582198293 | snp | A/C | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40982349 | AGTGTGGAGGTTAGC[A/C]ATGGTCAGCAGAAGC | 74164 |
| rs582343193 | snp | A/C | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41020427 | GTCCCATGTATCCAC[A/C]CTGAATAAACTCCAC | 74164 |
| rs582444389 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40997943 | ATTCCTAGGTTATTT[G/T]GAAGATGTAATAGTT | 74164 |
| rs582560735 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40981524 | TTTTGTTTTCCATCT[G/T]TTTGTTTGTTTGTTT | 74164 |
| rs582584223 | snp | A/C | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41023128 | AAGAAGAAGAAGAAG[A/C]AGCCAGTACAGCTTT | 74164 |
| rs582609263 | snp | C/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40968734 | GACCTGCTGTTTACA[C/T]GCATAATTTCACTTC | 74164 |
| rs582643007 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41014991 | TCATGTCAAACAACA[G/T]ACAGCTCTTTTCTAA | 74164 |
| rs582659917 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40985836 | AGATTTACTTATTCA[C/T]TATATGTAAGTACAC | 74164 |
| rs582703036 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | Nfx1 | GRCm38.p3 | 4:41012537 | ACTAGCTGCTTGAGT[C/T]CCTGCCTTGACTTAA | 74164 |
| rs582769489 | snp | A/G | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969550 | CTTGTCTCTCTCATC[A/G]TCATCATCTCACTAC | 74164 |
| rs582769660 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41001494 | GTGCTTCTCAGGCAC[G/T]CACCCCTCACTCAGC | 74164 |
| rs582882177 | snp | A/C | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40972916 | TTGTGGTGACCCCAA[A/C]CATAAAATTGTTTTG | 74164 |
| rs582882807 | snp | A/C | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41016743 | AAAATAAATAAATAT[A/C]TAAAAAAAAAAATTT | 74164 |
| rs582914426 | snp | A/C | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969735 | AGAAGCCCTGTAACC[A/C]AAATGGTCACATCGT | 74164 |
| rs583095116 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40974831 | GGCTCACAACCATCC[A/G]TAATGAGATCTGATG | 74164 |
| rs583126151 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40985967 | AAGAGCAGTCGGGTG[C/T]TCTTACCCACTGAGC | 74164 |
| rs583135624 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41001938 | AAATGTGTTTTAAAC[C/T]TTTTGATTTTATTTA | 74164 |
| rs583139724 | snp | C/T | | | utr-variant-3-prime | Nfx1 | GRCm38.p3 | 4:41025732 | TGTGGCCCCTCTTCT[C/T]CATAGGCTGGACTTA | 74164 |
| rs583159762 | snp | A/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41021352 | TAAATAGTTTTTTTA[A/T]AAAGTAGCTAGCTAA | 74164 |
| rs583162943 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40974859 | ATGCCCGCTTCTGGA[A/G]TGTCTGAAGACAGCT | 74164 |
| rs583238691 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40991325 | TTTTGTTTCACCACT[A/G]ATTAGAAACAGCAAA | 74164 |
| rs583270499 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41007124 | ACGTCAGTTCCTTGT[A/G]TTGGGGTGACCCCTA | 74164 |
| rs583320508 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40991416 | AATTAAAAAAATGGT[A/G]CGAGAGGCCAGTGAG | 74164 |
| rs583322567 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41022419 | GAAACAGTTAGCCTA[A/G]AGGGTTGTAGGAGAA | 74164 |
| rs583434682 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41023064 | TAATAATAATAATAA[G/T]AATAATAAGAAGAAG | 74164 |
| rs583559952 | snp | C/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41003325 | AGGCCTCCAACCCTA[C/G]TCCTGAGAAAGTTTG | 74164 |
| rs583633853 | snp | G/T | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | GRCm38.p3 | 4:40993093 | TTTTTTCCGAGACAG[G/T]GTTTCTCTGTGTAGC | 74164 |
| rs583650251 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40985884 | ACACCAGAAGAGGGC[A/G]TCAGATCTCATTACG | 74164 |
| rs583736225 | snp | C/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41007708 | CTAAAACACACCTCA[C/G]AGCCTGCAGGCAGCT | 74164 |
| rs583742516 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40974846 | ATAATGAGATCTGAT[A/G]CCCGCTTCTGGAGTG | 74164 |
| rs583752560 | snp | A/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969946 | CAGAGAAGATCCTAC[A/T]GCAAGGCCCGTGCCA | 74164 |
| rs583842707 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41016368 | GCCTGTGTGTGTGTG[C/T]GCGCGCGCGCATGTA | 74164 |
| rs583874758 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40991262 | TCCGTCCACGGTTCT[C/T]CTTCCTGCATGCTGC | 74164 |
| rs583929545 | snp | G/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40970212 | GACGCAGCACACACC[G/T]ATCACACACGGTGGA | 74164 |
| rs583935044 | snp | A/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41003512 | CCTCTGTAAAGACTC[A/T]AACTATTGAGCCATC | 74164 |
| rs584013331 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40971368 | CCGGCGGGCGGGCGG[A/G]CGGGCGGACGGCCGG | 74164 |
| rs584084259 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41013912 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 74164 |
| rs584189016 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40978010 | GAGCTCCTCAATCCT[C/T]TGTTGAGGATCACCC | 74164 |
| rs584286686 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40981600 | GCCTGTCCTGTCCTG[A/G]AGCTCACTCTGGTAG | 74164 |
| rs584290554 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41019853 | TGTGGATGTATGTCT[C/T]ACATGTACAGGGAGA | 74164 |
| rs584301248 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40990073 | TAACTAAAATTCCAT[G/T]TAGTAATTTTTTTTC | 74164 |
| rs584399621 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41023115 | GAAGAAGAAGAAGAA[G/T]AAGAAGAAGAAGAAG | 74164 |
| rs584408378 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41010584 | AGACACACCAGGCAT[C/T]AGATCCCATTACAGA | 74164 |
| rs584411938 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40994401 | AAAATGTAAATGTTT[A/G]GGAATAATGACGTTT | 74164 |
| rs584648317 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41005205 | CTTCCTGACCCTGGC[A/G]TTCCCCTGTACTGGG | 74164 |
| rs584791936 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40995663 | ATGACACCATGTCTC[C/T]AAAAACGGAAAGTTT | 74164 |
| rs584794269 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41023124 | GAAGAAGAAGAAGAA[G/T]AAGAAGCCAGTACAG | 74164 |
| rs584868537 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Nfx1 | GRCm38.p3 | 4:41011866 | GAAGCTCTGTGCCTG[C/T]GGATGCGAGTTGAAG | 74164 |
| rs584884569 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40980691 | CTACCCTTGTGTGTG[A/G]TGTGTTTGTGTATTG | 74164 |
| rs584886392 | snp | A/C | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40972566 | GTGGAGAACTTAGGC[A/C]GATACGTTGTCACTC | 74164 |
| rs584983314 | snp | A/C | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41018538 | GAGGAGGCAACCCCA[A/C]TTCCCCTCACCCTCT | 74164 |
| rs584990788 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40986095 | AACAGCATGTGTCTT[C/T]TCAAGTCAGTCTCCA | 74164 |
| rs584998326 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41019611 | TTTAATTTATTTATT[C/T]TGTGTAAGTGTTTTG | 74164 |
| rs585096632 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40974818 | GCAACCACATGGTGG[C/T]TCACAACCATCCATA | 74164 |
| rs585368477 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41005658 | CATGTGCACACGTAC[A/G]TGCACACACACACAC | 74164 |
| rs585387381 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40985883 | CACACCAGAAGAGGG[C/T]ATCAGATCTCATTAC | 74164 |
| rs585522368 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41002787 | TGTTAGATATATATG[C/T]ACTCCATCTACAGAA | 74164 |
| rs585524843 | snp | A/T | | | utr-variant-3-prime | Nfx1 | GRCm38.p3 | 4:41025078 | TGGCCACTGGATTTT[A/T]AATCATGTGTTTGAA | 74164 |
| rs585530311 | snp | A/G | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969553 | GTCTCTCTCATCATC[A/G]TCATCTCACTACTGC | 74164 |
| rs585532837 | snp | A/C | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41001528 | CCTGTATAACTACTG[A/C]TGCTGCCAGCATCCG | 74164 |
| rs585635064 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41023439 | TAGAACCAACCGCTA[A/G]CACCATCATCTGACG | 74164 |
| rs585652456 | snp | A/C | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969034 | CATAGCAAGAAAAAC[A/C]CAGCAACTCAACAGA | 74164 |
| rs585719079 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41007274 | TCCATCTACTTCCCC[C/T]AAAAAGAGGCAACAA | 74164 |
| rs585843705 | snp | A/G | | | utr-variant-3-prime | Nfx1 | GRCm38.p3 | 4:41025738 | CCCTCTTCTCCATAG[A/G]CTGGACTTATCTTTG | 74164 |
| rs585866447 | snp | G/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40969769 | GAATGTTTGAGACAG[G/T]GTTGTACTGTTGCTC | 74164 |
| rs585919597 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41005483 | TTTCAAAATTGAACA[C/T]TGTTTTTACAGAATT | 74164 |
| rs585976519 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40997946 | CCTAGGTTATTTGGA[A/G]GATGTAATAGTTTAA | 74164 |
| rs585985179 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41014714 | CCCTACCCCACCCCA[C/T]CCCCCCAAAAAAAGA | 74164 |
| rs585991845 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40983262 | TTTTTGTAAGTGGCT[G/T]AGTAATGCTTCATGG | 74164 |
| rs586076784 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41015448 | GGTAAGTGTTAACCC[A/G]CTGCTAGAGAGTCCA | 74164 |
| rs586087611 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40991258 | CCCATCCGTCCACGG[C/T]TCTCCTTCCTGCATG | 74164 |
| rs586177536 | snp | A/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40974837 | CAACCATCCATAATG[A/T]GATCTGATGCCCGCT | 74164 |
| rs586189603 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41019895 | TGTGTTTATGTGTCT[A/G]TGTGAATGTATGTCT | 74164 |
| rs586271477 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41016373 | TGTGTGTGTGTGCGC[A/G]CGCGCATGTACGTGT | 74164 |
| rs586448081 | snp | A/C | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41020730 | CAAAGCAAAACAGAA[A/C]AGCCAAAAGGCCAGT | 74164 |
| rs586492320 | snp | C/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41005485 | TCAAAATTGAACACT[C/G]TTTTTACAGAATTAA | 74164 |
| rs586498423 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40973237 | GAGGACATCTCACTA[A/G]TGGAGGAACTACTAC | 74164 |
| rs586542940 | snp | A/C | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41009719 | ATCAGATTCCCTGGT[A/C]CTGGAGTCACAGAGC | 74164 |
| rs586570517 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40991392 | GGGAGGCAGTGAGGA[A/G]AATATTGAAATTAAA | 74164 |
| rs586655415 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40985894 | AGGGCATCAGATCTC[A/G]TTACGGATGGTTGTG | 74164 |
| rs586734602 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40986665 | ATTCCTATTCATTCT[C/T]TCTTCTCCCCCCCCC | 74164 |
| rs586761746 | snp | C/T | | | upstream-variant-2KB | Nfx1 | GRCm38.p3 | 4:40970493 | CCCAGGACCTGGAAC[C/T]CACTACATCCCACTC | 74164 |
| rs586925362 | snp | A/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41010842 | CAACTGATTTTATAT[A/T]TATATATATTCTGAC | 74164 |
| rs586931469 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40978188 | CTGTTTGGATTGTTG[A/G]TTTTTGTGTTTGTTT | 74164 |
| rs587039804 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40986087 | TTTCCTGTAACAGCA[G/T]GTGTCTTCTCAAGTC | 74164 |
| rs587115437 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41018548 | CCCCACTTCCCCTCA[C/T]CCTCTGTCCTGGGTC | 74164 |
| rs587151875 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41003386 | GGTCAGTGTGGAGGC[A/G]TGTACACATGAGTGC | 74164 |
| rs587204723 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nfx1, Mir3094 | GRCm38.p3 | 4:40993100 | CGAGACAGTGTTTCT[C/T]TGTGTAGCCCTGGCT | 74164 |
| rs587223805 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41022829 | CTAAAGATGAAGATC[A/G]GGGGGACAGACTGCC | 74164 |
| rs587243549 | snp | C/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40991417 | ATTAAAAAAATGGTA[C/G]GAGAGGCCAGTGAGA | 74164 |
| rs587527824 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41023067 | TAATAATAATAATAA[G/T]AATAAGAAGAAGAAG | 74164 |
| rs587547762 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41004169 | CCAGCTCCAGGGAGT[A/G]CTCTGCTCAGTCTCG | 74164 |
| rs587582184 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41007726 | CCTGCAGGCAGCTCA[A/G]CAGATTGGAGCTTTC | 74164 |
| rs587586680 | snp | G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40974850 | TGAGATCTGATGCCC[G/T]CTTCTGGAGTGTCTG | 74164 |
| rs864257138 | in-del | -/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41002104 | CAACACCCAATACTG[-/T]TTTTTTGTTCTTTTT | 74164 |
| rs864274698 | snp | A/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40999866 | TTATGGTAAAAGGAG[A/G]AAAAAATTACCCATT | 74164 |
| rs864275969 | snp | A/G/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41024303 | GGGGCGAGGCGGGGG[A/G/T]TAGACAAACAAAGTG | 74164 |
| rs864286387 | snp | A/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41015776 | TTGGTTGGACCTGCG[A/T]CAGATCTGTACACTG | 74164 |
| rs864289839 | snp | A/C/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41019763 | CTGAATCTAGGCTGT[A/C/G]TGCAAGAGCAACAAG | 74164 |
| rs864293958 | snp | C/T | | | intron-variant | Nfx1 | GRCm38.p3 | 4:41001136 | TATGCTCTTGATGCC[C/T]GACCCCTTGGTGCCG | 74164 |
| rs864297132 | snp | A/C/G | | | intron-variant | Nfx1 | GRCm38.p3 | 4:40971380 | CGGGCGGGCGGACGG[A/C/G]CGGCCGGCCGGGCGT | 74164 |
| rs864297696 | snp | A/T | | | utr-variant-3-prime, intron-variant | Nfx1 | GRCm38.p3 | 4:41013739 | AAAGCCAGCCTGTAC[A/T]GCAAGAGCCTATTTT | 74164 |