SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6284127 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Ncf2 | Mm_Celera | 1:152817795 | GGACAACTTCTTCCC[A/G]CTATTACTAAAAAGG | 17970 |
rs13466541 | snp | C/T | 0.497778 | 0.0332592 | synonymous-codon | Ncf2 | Mm_Celera | 1:152831634 | TACCTCTCCAGAATC[C/T]GATATTCCACCACCT | 17970 |
rs31171944 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ncf2 | Mm_Celera | 1:152828107 | GCAAGCCATCTTCCT[C/T]CTCCAATAAAGGGGG | 17970 |
rs31171945 | snp | A/C | 0.5 | 0 | intron-variant | Ncf2 | Mm_Celera | 1:152828069 | agaaaaaagaaaaaa[A/C]CAAAATCCTTCTAAG | 17970 |
rs31171946 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152827823 | TCACTCAGTAAACCC[A/G]AGAAGCAGAGCGGCC | 17970 |
rs31171947 | snp | C/T | 0.5 | 0 | intron-variant | Ncf2 | Mm_Celera | 1:152827757 | AGCTATCACAGTCTC[C/T]TTCCTGTGTGCGTTT | 17970 |
rs31171948 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152827663 | ATTGCTTCGAAGCCC[A/G]GGTCAGAGGTGAGAG | 17970 |
rs31171949 | snp | C/G/T | 0.48 | 0.0979796 | intron-variant | Ncf2 | GRCm38.p3 | 1:152827655 | GGGAGGTCATTGCTT[C/G/T]GAAGCCCAGGTCAGA | 17970 |
rs31171950 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ncf2 | Mm_Celera | 1:152827577 | AGACCCAAATGATGC[C/G]ATTGTGCTGAGACCA | 17970 |
rs31171951 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152827576 | TAGACCCAAATGATG[C/T]GATTGTGCTGAGACC | 17970 |
rs31171952 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152827505 | ATACCCTCACTCTAC[A/G]TCTGACTTGACGGCA | 17970 |
rs31171953 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ncf2 | Mm_Celera | 1:152827504 | AATACCCTCACTCTA[C/T]GTCTGACTTGACGGC | 17970 |
rs31172484 | snp | G/T | 0.142012 | 0.225474 | utr-variant-5-prime, intron-variant | Ncf2 | Mm_Celera | 1:152807431 | ATGGACACTGAAGAT[G/T]CTCCATCCTGTCTCA | 17970 |
rs31172485 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ncf2 | Mm_Celera | 1:152807254 | CTAAATCTGTGTTTA[C/T]AGAGACTAGTGAACT | 17970 |
rs31172486 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152807212 | TAAATTAACTTTGAC[A/T]TTACCAGGGCAGTAA | 17970 |
rs31172487 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ncf2 | Mm_Celera | 1:152806879 | CCAGGCAAAGAAGTG[A/G]GATAGGAAGGCCTGC | 17970 |
rs31172488 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152806835 | ACATAGGAGACTGGA[C/T]GAATGAGCCTGGAAG | 17970 |
rs31172489 | snp | A/G | 0.42 | 0.183303 | intron-variant | Ncf2 | Mm_Celera | 1:152806796 | CGTAATGTAGAGTGC[A/G]GAGTGGACTGTCGCA | 17970 |
rs31172490 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Ncf2 | Mm_Celera | 1:152806777 | AAAGGGACAATACTC[C/T]CTCCGTAATGTAGAG | 17970 |
rs31172491 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152806354 | GCTTATAAAAAGCCT[A/T]GTTTGGCTACAAGTC | 17970 |
rs31172492 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Ncf2 | Mm_Celera | 1:152806257 | AAATCACTTGGAAGT[C/T]TAAATGTCAGGCTAG | 17970 |
rs31172493 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Ncf2 | Mm_Celera | 1:152806243 | CTGAGAAGCCAAGGA[A/G]ATCACTTGGAAGTTT | 17970 |
rs31172814 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152827488 | TTAGGTCTGCATGCG[A/G]AATACCCTCACTCTA | 17970 |
rs31172815 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152827311 | GTTTTTGGATCTGGA[A/G]CAGTATTCCAAATTA | 17970 |
rs31172816 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152827291 | CACCCAGAAAAGAAG[G/T]CTTTGTTTTTGGATC | 17970 |
rs31172817 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152827252 | GGCTTTTGGTTTCCC[A/G]AATTGTGCCCTTGCC | 17970 |
rs31172818 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152827212 | AGCAGCTTCACTGGC[A/G]AGGGTCAGGCCCAGG | 17970 |
rs31172819 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ncf2 | Mm_Celera | 1:152827148 | ATACTGGGGAAGGGT[C/T]GAGTTGAGGTCAATA | 17970 |
rs31172820 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ncf2 | Mm_Celera | 1:152827121 | TTAATTGTAGACCAG[C/T]GCTTTTGGAAAATAC | 17970 |
rs31172821 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ncf2 | Mm_Celera | 1:152827098 | AATGTCACATATTGT[A/G]GCAAACATTAATTGT | 17970 |
rs31172822 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ncf2 | Mm_Celera | 1:152827054 | TCTTGTCTGGCCAGG[A/G]GATGCTGAGTTGATT | 17970 |
rs31172823 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152826292 | CCATTTGCTCCTGTA[C/T]AAGAGACTCCTTTGG | 17970 |
rs31173304 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152806145 | CTAGCTCTGAAGGCT[A/G]GGTTGGGTAAGTCTC | 17970 |
rs31173305 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Ncf2 | Mm_Celera | 1:152806070 | GGACTTGGGAAAGAA[A/G]ACGAGGTCATGGGCT | 17970 |
rs31173306 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152806009 | GACACAAGAGCATAT[A/G]TAACTGCATGGGTGG | 17970 |
rs31173307 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ncf2 | Mm_Celera | 1:152805870 | TTCAGCCTATATGGT[A/G]ACAGGGACTAGAGAA | 17970 |
rs31173308 | snp | C/T | 0.5 | 0 | intron-variant | Ncf2 | Mm_Celera | 1:152805855 | GTTAACTGATGGTAT[C/T]TCAGCCTATATGGTG | 17970 |
rs31173309 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152805726 | ACCTGCCAGTCCCAC[A/G]AGGAGTCTGGAAAGA | 17970 |
rs31173310 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ncf2 | Mm_Celera | 1:152805148 | GAGGGAGTGGCCCTT[A/G]CAGCTGGGACACAAG | 17970 |
rs31173311 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ncf2 | Mm_Celera | 1:152805064 | ACTGTGTGCTGTGTG[A/G]GTCATGGCGGCCAGT | 17970 |
rs31173312 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Ncf2 | Mm_Celera | 1:152805028 | CATCATTACGAGCTG[A/G]CCCACAGGCTGTCGG | 17970 |
rs31173313 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152804922 | AGAACTTGGGTTCTG[A/T]CATAAGGACGCTTGG | 17970 |
rs31173634 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152826153 | GACCACCTCATGGGA[C/G]CTTGCGCAGCCTCTG | 17970 |
rs31173635 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ncf2 | Mm_Celera | 1:152826116 | TCTCCCGTCCTCTGC[C/T]GGTGGTCCTAAGAGA | 17970 |
rs31173636 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ncf2 | Mm_Celera | 1:152826099 | CGGCCCTGTCAGCTC[C/T]GTCTCCCGTCCTCTG | 17970 |
rs31173637 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152826010 | AAACTGATCACAGGG[A/G]TTCAGCCGCCTCTCA | 17970 |
rs31173638 | snp | C/T | 0.5 | 0 | intron-variant | Ncf2 | Mm_Celera | 1:152825866 | AGCAGCACGCTCACC[C/T]TCTTGTCTGTTTCAG | 17970 |
rs31173639 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152825859 | GCCTGGCAGCAGCAC[C/G]CTCACCTTCTTGTCT | 17970 |
rs31173640 | snp | A/G | 0.5 | 0 | intron-variant | Ncf2 | Mm_Celera | 1:152825674 | TGATGTTGTATGACT[A/G]CCAGCAGTTTTTCAT | 17970 |
rs31173641 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152824824 | TATTTGGCTTTGACA[A/G]TTTGGACATGTGAGT | 17970 |
rs31173642 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152824809 | ACCTTATCTGATCTG[C/T]ATTTGGCTTTGACAA | 17970 |
rs31173643 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Ncf2 | Mm_Celera | 1:152824629 | GAGTCGGGAGAGGGC[C/T]AGCAGGAGATGCCCT | 17970 |
rs31174184 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ncf2 | Mm_Celera | 1:152804856 | TGGGGCATTGTGGGA[A/G]ATGTGATATGACTGA | 17970 |
rs31174185 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Ncf2 | Mm_Celera | 1:152804790 | CCAACCCTACATCCC[C/T]GACTTGGATTGGGGA | 17970 |
rs31174186 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ncf2 | Mm_Celera | 1:152804755 | ACCACGCTCGGCTGT[A/G]CATCAGTTTTACATT | 17970 |
rs31174187 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152802697 | GTCATGGGTCGATAA[G/T]GCTTCAGGAGTTACA | 17970 |
rs31174188 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152802629 | ATCACATGGTTTTTA[A/C]AGCATTCTTACATTC | 17970 |
rs31174189 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Ncf2 | Mm_Celera | 1:152801737 | GCCAACCAAATAAAA[C/T]AGCAGTCATGATTTT | 17970 |
rs31174190 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152801720 | TGTGACTAGGGTAGT[A/C]TGCCAACCAAATAAA | 17970 |
rs31174191 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152801567 | AATTACCCATTCAGC[C/T]AATCATGAGAGTTTT | 17970 |
rs31174192 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152801547 | TCTCAATTGTTTATT[C/T]GGTTAATTACCCATT | 17970 |
rs31174193 | snp | G/T | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152801029 | CTCAGAATGTTAGGT[G/T]CTAGGTTCTGTGGGA | 17970 |
rs31174494 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152824561 | GGTTTCTACTGGGAT[G/T]CTGAGTCTTGGGACA | 17970 |
rs31174495 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152824517 | TCTCTCCAGCTTCTT[C/T]CATAACCCTGACCAT | 17970 |
rs31174496 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152824147 | TGCTCACATGAGCTC[A/G]CCTAATAACGTCTGG | 17970 |
rs31174497 | snp | C/T | 0.5 | 0 | intron-variant | Ncf2 | Mm_Celera | 1:152823955 | TGGTTGGAAAGGACT[C/T]TTCTTTTGATATGTT | 17970 |
rs31174498 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ncf2 | Mm_Celera | 1:152822488 | GAGAGTGTTGGGTAA[A/G]TAATACCAATATAAG | 17970 |
rs31174499 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ncf2 | Mm_Celera | 1:152821926 | CCTGAAGTCCTGGCT[A/G]TCCAGCACAGTGCCA | 17970 |
rs31174500 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152821878 | GGGGATGTGCAGCCT[A/C]TAAACACGGTGAAGA | 17970 |
rs31174501 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152821799 | AAGCCACACCCTAGC[A/G]AATGGAACAGTACAG | 17970 |
rs31174502 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Ncf2 | Mm_Celera | 1:152821479 | GGTGCCTGGTTTTGG[A/T]GCAGATTCAAGATTT | 17970 |
rs31174503 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152821168 | GCAAGAGCAGGAATT[C/T]GACATCACACACTCA | 17970 |
rs31175104 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ncf2 | Mm_Celera | 1:152800826 | CATATGCGATCCCAG[C/T]GCAATCATGAAAGAA | 17970 |
rs31175105 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Ncf2 | Mm_Celera | 1:152800814 | CCGAAGAAACTGCAT[A/C]TGCGATCCCAGCGCA | 17970 |
rs31175106 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ncf2 | Mm_Celera | 1:152800768 | AGCCTTAGATGTCCT[C/T]GGTGCGAGAGTCCTT | 17970 |
rs31175107 | snp | A/G | 0.197531 | 0.244432 | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800325 | GTGTGTTTCTAACTC[A/G]TCACACTCTTCCTTT | 17970 |
rs31175108 | snp | C/T | 0.396694 | 0.202437 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799786 | ACCACATGCTTTCAG[C/T]TGCTACAACAGAGGA | 17970 |
rs31175109 | snp | C/G | 0.32 | 0.24 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799783 | ATGACCACATGCTTT[C/G]AGCTGCTACAACAGA | 17970 |
rs31175110 | snp | C/T | 0.473373 | 0.11227 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799777 | TGCAGAATGACCACA[C/T]GCTTTCAGCTGCTAC | 17970 |
rs31175111 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799748 | TCACTTACTGTCATA[C/T]GTTGGCAGACACATG | 17970 |
rs31175112 | snp | C/T | 0.489796 | 0.070696 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799691 | TGCTTTTGCTGTGGT[C/T]CAGACAACAGATCCC | 17970 |
rs31175113 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799663 | GGGAGTGTTTCGGTC[C/T]AAATGTGGGCCGTGC | 17970 |
rs31175364 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152820491 | TAATAAAGCAGACAC[C/T]GAGGAACCCACAATT | 17970 |
rs31175365 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Ncf2 | Mm_Celera | 1:152820446 | ATGTACAAAAGTGTA[A/G]TTGGTTCTTGTATGC | 17970 |
rs31175366 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152820352 | CTAGCATGGTAGAAT[C/T]GTTTGTTGGCAAGGA | 17970 |
rs31175367 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152818652 | TTTCTGTCACCTGTA[A/G]TAAATAGTAACGGGC | 17970 |
rs31175368 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152818210 | TCCCTCCATAAGTTG[A/G]AGCAAACGCTTTGTT | 17970 |
rs31175369 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152818140 | CAAGGGAAGACTTGC[A/C]TTTGCTTTGGGAATT | 17970 |
rs31175370 | snp | A/G/T | 0.497041 | 0.0383476 | intron-variant | Ncf2 | GRCm38.p3 | 1:152818136 | CTCACAAGGGAAGAC[A/G/T]TGCATTTGCTTTGGG | 17970 |
rs31175371 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152817675 | GAACCTGCTGTAACC[C/T]GCCTAGGTACTTGAT | 17970 |
rs31175372 | snp | A/T | 0.495868 | 0.0452663 | intron-variant | Ncf2 | Mm_Celera | 1:152817652 | ATCATGGGTTCTCTG[A/T]CTGTGAGGAACCTGC | 17970 |
rs31175373 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152817293 | CCAGGATCTGACACC[A/G]GCATTGACAAAGGGA | 17970 |
rs31175872 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152837455 | GGACTGGAGCAGCAC[A/G]GACAGTTTCTTTTGC | 17970 |
rs31175873 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152837335 | GAATCAGTGACATTT[C/T]CAACCTCGGAATGCT | 17970 |
rs31175984 | snp | C/G/T | 0.497041 | 0.0383476 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799618 | GAACTTCACAGGCCT[C/G/T]GCTGTGTGTCCATTG | 17970 |
rs31175985 | snp | A/G | 0.497041 | 0.0383476 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799259 | AAATCCAAAACAAAA[A/G]GCAAGCTTGATGGCA | 17970 |
rs31175986 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799176 | AGGTTTGGTCTCTCA[A/G]ATGGCCAGTCTGGCC | 17970 |
rs31175987 | snp | A/G | 0.408163 | 0.193609 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799096 | AAGTAGCCAGGAAGT[A/G]TCCTCTGGCCAAGGA | 17970 |
rs31175988 | snp | A/G | 0.18 | 0.24 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799080 | ATTAACTATTGATAG[A/G]AAGTAGCCAGGAAGT | 17970 |
rs31175989 | snp | G/T | 0.497041 | 0.0383476 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799059 | AAACAGTCAGACTAA[G/T]CTTTGATTAACTATT | 17970 |
rs31175990 | snp | C/T | 0.459184 | 0.136902 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798999 | AAGCTGAGAGGTGGG[C/T]GCTCTGAAATAAGGC | 17970 |
rs31175991 | snp | C/T | 0.486111 | 0.0821678 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798855 | CCAATCCTGACACAG[C/T]AAGGACAGAAAGGGA | 17970 |
rs31175992 | snp | G/T | 0.497041 | 0.0383476 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798817 | CTCTTTATTACAAGC[G/T]CAGGCTTGGGCTCTC | 17970 |
rs31175993 | snp | C/T | 0.489796 | 0.070696 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798755 | CCAGGAACCACGAAC[C/T]CCAAAAGATCACCAA | 17970 |
rs31176374 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ncf2 | Mm_Celera | 1:152817220 | TGTTAAGAAAACACT[A/G]AGATGCGTGTAGCTT | 17970 |
rs31176375 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Ncf2 | Mm_Celera | 1:152817195 | TCTGTGCCTCGAGCC[A/G]CATGCTGTCTGTTAA | 17970 |
rs31176376 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Ncf2 | Mm_Celera | 1:152817073 | TACAAGATCCTGGGG[C/T]TGCAGTTCAAGCTGT | 17970 |
rs31176377 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ncf2 | GRCm38.p3 | 1:152816967 | CCTGCATGGGACCAG[C/T]TCTCTTCTCCTCCTG | 17970 |
rs31176378 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ncf2 | Mm_Celera | 1:152816807 | CATAGACGGAAGGTC[C/T]CCACAAGCTGTGCTG | 17970 |
rs31176379 | snp | C/G | 0.42 | 0.183303 | intron-variant | Ncf2 | Mm_Celera | 1:152816565 | GGCAGGAGGATGGTA[C/G]CCACAGCTATAGCTG | 17970 |
rs31176380 | snp | G/T | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152816335 | AATTGTATCTGCTCA[G/T]AGAACAGGACACCTG | 17970 |
rs31176381 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152816232 | TCTGCAGGGAGCAAG[A/G]CACGATTGTACTGTT | 17970 |
rs31176382 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Ncf2 | Mm_Celera | 1:152816055 | CTCCTTCTTACAAAA[C/T]AAGCACTCTGGGTAA | 17970 |
rs31176383 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ncf2 | GRCm38.p3 | 1:152815643 | CCTCTTTCAAAACTG[A/G]TCCTACTCAGACCTG | 17970 |
rs31176704 | snp | A/G | 0.408163 | 0.193609 | utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152837203 | AAGGCGAGGAACCCC[A/G]CCGAGAGAGTCATAA | 17970 |
rs31176705 | snp | A/C | 0.497778 | 0.0332592 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152836990 | AAATCCTCTACACAC[A/C]GATCTGCTTGGAGAG | 17970 |
rs31176706 | snp | C/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152836939 | CAGTTGAAGTTCTAA[C/G]CTGTATTTTTACTGC | 17970 |
rs31176707 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152836599 | TCAGGTTCCCATGAA[A/G]CACACCATCCAGTCC | 17970 |
rs31176708 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152836579 | TAAAGAAAAGGCAGA[C/T]TGAATCAGGTTCCCA | 17970 |
rs31176709 | snp | A/G | 0.48 | 0.0979796 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152836578 | TTAAAGAAAAGGCAG[A/G]TTGAATCAGGTTCCC | 17970 |
rs31176710 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime | Ncf2 | Mm_Celera | 1:152836314 | ACAAATTTTCTGCAA[A/G]GGAAATGAAGGTTTG | 17970 |
rs31176711 | snp | A/C | 0.497778 | 0.0332592 | utr-variant-3-prime | Ncf2 | Mm_Celera | 1:152836210 | AGTTTGGAAATGTGG[A/C]CTAACTTACCATTTC | 17970 |
rs31176712 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Ncf2 | Mm_Celera | 1:152836178 | CCCATCTCTGCTGTG[C/T]GCTATACAGACACAC | 17970 |
rs31176713 | snp | A/G/T | 0.387812 | 0.208586 | utr-variant-3-prime | Ncf2 | GRCm38.p3 | 1:152836137 | AAAGCTGAAGCAAAG[A/G/T]GTTGTTTTTCCCCTT | 17970 |
rs31176864 | snp | C/G | 0.497778 | 0.0332592 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798723 | AGGAGGCAGATCTCT[C/G]AGTTAGATGTGTTGT | 17970 |
rs31176865 | snp | A/G | 0.459184 | 0.136902 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798561 | CCTATTTTTTCCCTC[A/G]GGAGGATAAACATTT | 17970 |
rs31176866 | snp | A/G | 0.426035 | 0.177515 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798337 | TCCCCAAACAGGTTC[A/G]GTTGAGCCAACTACA | 17970 |
rs31176867 | snp | C/T | 0.497778 | 0.0332592 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798278 | TACTTCCTGAAATGA[C/T]GGAGGCTATTGTTTA | 17970 |
rs31176868 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798237 | AAAAAAGTGCCTCGG[A/G]CCTGTAAACCCTGGC | 17970 |
rs31177414 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Ncf2 | GRCm38.p3 | 1:152815586 | GAAGCCTCCAGATGG[C/T]AGAGGAGGGCACTTG | 17970 |
rs31177415 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ncf2 | GRCm38.p3 | 1:152815301 | AGGAGGTAAAGCCTT[C/T]TTCCTGCTGGGCTGA | 17970 |
rs31177416 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | GRCm38.p3 | 1:152815243 | TGGAAATAAAAGCAG[A/G]GTGAGACCTTTCAGA | 17970 |
rs31177417 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Ncf2 | GRCm38.p3 | 1:152815023 | CTTCAGTGTTGCTTG[C/T]CTTAAATTCTAGCAG | 17970 |
rs31177418 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ncf2 | GRCm38.p3 | 1:152814925 | GGTTAGGCATTCCTT[C/T]CCATTGCACTGGGGC | 17970 |
rs31177419 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Ncf2 | GRCm38.p3 | 1:152813183 | TACACCAGAAGATGT[A/G]GCTGCGGCTTTTCTT | 17970 |
rs31177420 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ncf2 | GRCm38.p3 | 1:152812346 | TTTGATAGAGGGTGG[C/T]GCCTTAAGGATAACA | 17970 |
rs31177421 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Ncf2 | GRCm38.p3 | 1:152812314 | GCAGCTGGATACTTA[C/T]AGACCGAGCTGAGTG | 17970 |
rs31177422 | snp | C/T | 0.5 | 0 | intron-variant | Ncf2 | GRCm38.p3 | 1:152812284 | CATATTTTGAGTGGA[C/T]TCTGTCATGCAGCAG | 17970 |
rs31177423 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Ncf2 | Mm_Celera | 1:152812270 | AGGCACAGGGCTGGC[A/G]TATTTTGAGTGGATT | 17970 |
rs31177614 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152835797 | GAGGCTTCATGTTCA[A/G]TCTTATTCATTCTAC | 17970 |
rs31177615 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152835713 | GCTTACCACCATGCC[C/T]TTTCATGTTATCAAA | 17970 |
rs31177616 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152835564 | CAGGAAGGGTACCAT[C/T]CTTGTGAAAATCTGG | 17970 |
rs31177617 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152835495 | TGCAGAGGCAGCCAA[C/T]TGTCAGTGACTTACC | 17970 |
rs31177618 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152835438 | CTGTCTCTGCTAGAA[A/C]CCATCAAGTACTTTC | 17970 |
rs31177619 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ncf2 | Mm_Celera | 1:152835293 | ACACCAACTCTTAGC[C/T]AATCTCTTCCTAGAT | 17970 |
rs31177620 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ncf2 | Mm_Celera | 1:152834949 | TATAAGGAAGTATTG[A/C]GCATCAATTGCTTCC | 17970 |
rs31177621 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152834783 | TTATTTGTGGCTCAA[A/T]ATCATTTCCCAATCT | 17970 |
rs31177622 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152834742 | ATATGATAAAAACTA[C/G]TTGAATTTATACCAC | 17970 |
rs31177623 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152834366 | TACGGCTGCCTTCAC[A/T]AGACTGACTGGGTCA | 17970 |
rs31178304 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152812181 | CAGACGTCCTCAGGA[A/G]CAATGAGGGTCAGAA | 17970 |
rs31178305 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152812102 | CAGATCACTGAGGGA[A/T]TAAGTCACTCTAGAC | 17970 |
rs31178306 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152811988 | AAGAATTTCCCATCA[A/G]TGAAACTGGACAAGT | 17970 |
rs31178307 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152811865 | ACATGTACACACAGA[C/T]ATATCAAAAGGATAA | 17970 |
rs31178308 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152811603 | CAAAACCCATTTGTT[A/G]CACAGTCTGGAAGGG | 17970 |
rs31178309 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ncf2 | Mm_Celera | 1:152811479 | CTGTTAGCAGCAGAT[A/G]TATAAGTTAATACAG | 17970 |
rs31178310 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152811358 | GGCTCATCATGAAAG[C/T]GAATCAATCCTGGCT | 17970 |
rs31178311 | snp | C/T | 0.5 | 0 | intron-variant | Ncf2 | Mm_Celera | 1:152811310 | GGACGTTCACTGTGC[C/T]TCTCTGTGCGGGACT | 17970 |
rs31178312 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Ncf2 | Mm_Celera | 1:152811224 | ATCATTAGCGCACAG[C/T]GGCAAGGAGCCTGAA | 17970 |
rs31178313 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Ncf2 | Mm_Celera | 1:152811221 | GTCATCATTAGCGCA[C/G]AGCGGCAAGGAGCCT | 17970 |
rs31178384 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ncf2 | Mm_Celera | 1:152834295 | GTTATAGCAGGCATC[A/G]GATAGCAGTTATAGA | 17970 |
rs31178385 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ncf2 | Mm_Celera | 1:152834227 | TTTTAACATCTCCTG[C/T]ATGCCACACATTGGC | 17970 |
rs31178386 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ncf2 | Mm_Celera | 1:152834214 | GACCTAAGGCCATTT[C/T]TAACATCTCCTGTAT | 17970 |
rs31178387 | snp | A/C/G | 0.497778 | 0.0332592 | synonymous-codon | Ncf2 | GRCm38.p3 | 1:152834108 | GCTTCTGCTCCTGTC[A/C/G]GAAGAAAGCATGAAG | 17970 |
rs31178388 | snp | A/G | 0.497778 | 0.0332592 | missense | Ncf2 | Mm_Celera | 1:152834074 | TCCCTACCAGCTACC[A/G]GCGTCGGGACAGCCA | 17970 |
rs31178389 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ncf2 | Mm_Celera | 1:152834032 | GTTTTTTGTGTTGAT[A/G]CTTTCTGCCTTGGTC | 17970 |
rs31178390 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152833944 | GTAAACCCCATGAAG[C/T]CGGGAGCTGGGGATG | 17970 |
rs31178391 | snp | C/T | 0.497778 | 0.0332592 | synonymous-codon | Ncf2 | Mm_Celera | 1:152833920 | CTCGCCAGAACACAC[C/T]AAACTGAGGTAAACC | 17970 |
rs31178392 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Ncf2 | Mm_Celera | 1:152833599 | ATATACAGTTGTCTA[C/T]TGATTTTTTAACTTA | 17970 |
rs31178393 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ncf2 | Mm_Celera | 1:152833490 | TCCTAGCCCCTAGCT[A/G]AGCACATAGCTCAGT | 17970 |
rs31179174 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152811094 | TTCAATCAGGACCTC[C/G]AGCTTTTGTGGGTAG | 17970 |
rs31179175 | snp | C/T | 0.18 | 0.24 | intron-variant | Ncf2 | Mm_Celera | 1:152811093 | ATTCAATCAGGACCT[C/T]CAGCTTTTGTGGGTA | 17970 |
rs31179176 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Ncf2 | Mm_Celera | 1:152811034 | CTCAGGCTGTGGGAG[C/T]GTGACAGCGCCTGAT | 17970 |
rs31179177 | snp | A/C | 0.497041 | 0.0383476 | synonymous-codon | Ncf2 | Mm_Celera | 1:152810926 | CCTGCAGGCCTTCAC[A/C]AAAAGCATCAACAGA | 17970 |
rs31179178 | snp | C/T | 0.42 | 0.183303 | intron-variant | Ncf2 | Mm_Celera | 1:152810872 | ACAAGTCTTGCCTCT[C/T]CCTGGCAATACTCTG | 17970 |
rs31179179 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152809968 | AAAAAACACATCCAC[A/G]TCCTGACAGGAGGAG | 17970 |
rs31179180 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152809955 | TGACCAGCCAGTGAA[A/C]AAACACATCCACATC | 17970 |
rs31179181 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152808634 | GAATTCTGAGGCTAG[C/T]TGAGGAAACTCACAC | 17970 |
rs31179182 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ncf2 | Mm_Celera | 1:152808613 | CAAGGCAGGGTTCTT[C/T]TTTAAGAATTCTGAG | 17970 |
rs31179183 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152808552 | CTTCCAGGAACTTAC[A/G]CAACATCCTATCAGT | 17970 |
rs31179204 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Ncf2 | Mm_Celera | 1:152833239 | CCTCTAGATCCACCC[C/T]GGATGTTAAAGGGTA | 17970 |
rs31179205 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ncf2 | Mm_Celera | 1:152833096 | GGGTTATCACACGTC[C/T]ATCTTCCCTCTGTCT | 17970 |
rs31179206 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Ncf2 | Mm_Celera | 1:152832989 | ATACACACTTTGCTG[C/T]GCTAACATAGTGTGC | 17970 |
rs31179207 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ncf2 | Mm_Celera | 1:152832981 | CTTCACTTATACACA[C/T]TTTGCTGTGCTAACA | 17970 |
rs31179208 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Ncf2 | Mm_Celera | 1:152832959 | CTCAGTAGTAAAGGG[C/T]CTCAGACTTCACTTA | 17970 |
rs31179209 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Ncf2 | Mm_Celera | 1:152832956 | ATCCTCAGTAGTAAA[C/G]GGTCTCAGACTTCAC | 17970 |
rs31179210 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Ncf2 | Mm_Celera | 1:152832924 | ATTCGAATAATCAGC[A/T]GCACAGAGGTTCTTC | 17970 |
rs31179211 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ncf2 | Mm_Celera | 1:152832690 | AGGATAGAAGTCCCC[C/T]GGGAACAAGCATGGC | 17970 |
rs31179212 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ncf2 | Mm_Celera | 1:152832538 | TGTCAGGGCGTGTGC[C/T]CTTGCATCACAAACA | 17970 |
rs31179213 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152832420 | CTCCACAGTCAAAGA[C/T]GCTTGCTGCACAGTC | 17970 |
rs31180024 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152832318 | TTATTTGGAAAGCTG[C/T]GAACCTACAGAGAAG | 17970 |
rs31180025 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Ncf2 | Mm_Celera | 1:152832146 | GGATGGTGTGGATGG[A/G]AGATCTTCCCAGAAG | 17970 |
rs31180026 | snp | G/T | 0.18 | 0.24 | intron-variant | Ncf2 | Mm_Celera | 1:152832103 | TGTCTGCAGAGCAGA[G/T]CCCCCAGGGCTTGAA | 17970 |
rs31180027 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152832018 | TAACTACCTAAAGCC[G/T]GTGGGAGGAAAAAGG | 17970 |
rs31180028 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152831994 | AGCAGTCACCAGGTG[A/G]TCCTTTGCTAACTAC | 17970 |
rs31180029 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152831980 | GTGGCCATCATCAGA[A/G]CAGTCACCAGGTGAT | 17970 |
rs31180030 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152831958 | GTGCAGGTAATGGGG[C/T]CCGCCAGTGGCCATC | 17970 |
rs31180031 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Ncf2 | Mm_Celera | 1:152831953 | AATGAGTGCAGGTAA[A/T]GGGGCCCGCCAGTGG | 17970 |
rs31180032 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152831906 | CATCCCCCTGAAACA[C/T]GATGGCAGTGCCCTG | 17970 |
rs31180033 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ncf2 | Mm_Celera | 1:152831873 | TTTCCAGAGCCCTGT[C/G]TTGCTTGCACCATCC | 17970 |
rs31180144 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ncf2 | Mm_Celera | 1:152808510 | CACCATAAACCCTTG[C/T]ATCCAGTTGTAAAAT | 17970 |
rs31180145 | snp | A/C | 0.486111 | 0.0821678 | intron-variant | Ncf2 | Mm_Celera | 1:152808469 | TGTGTTTTCTTTTAC[A/C]TCGCCTCCTGGATAA | 17970 |
rs31180146 | snp | C/T | 0.18 | 0.24 | intron-variant | Ncf2 | Mm_Celera | 1:152808410 | TATGAGATCTCCTTA[C/T]TACCCAAGATCATCT | 17970 |
rs31180147 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ncf2 | Mm_Celera | 1:152808349 | GCAGTTTTAAAAGCT[C/T]CCAGGGCAGGTTTTC | 17970 |
rs31180148 | snp | C/T | 0.497041 | 0.0383476 | synonymous-codon | Ncf2 | Mm_Celera | 1:152808175 | AGGCTGCGTGAACAC[C/T]ATCCTGGAAAACTTG | 17970 |
rs31180149 | snp | G/T | 0.5 | 0 | missense | Ncf2 | Mm_Celera | 1:152808100 | CAAGAAGGACTGGAA[G/T]GGTGCCCTGGAGGCC | 17970 |
rs31180150 | snp | C/T | 0.497041 | 0.0383476 | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152807900 | AACTTCCTGACGCTA[C/T]GAAGTCGCCCAAAGG | 17970 |
rs31180151 | snp | C/T | 0.497041 | 0.0383476 | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152807856 | TCTCTCTCATGCTAG[C/T]TTATGCGTCAGTTCC | 17970 |
rs31180152 | snp | A/G | 0.142012 | 0.225474 | utr-variant-5-prime, intron-variant | Ncf2 | Mm_Celera | 1:152807631 | GCAAGTCTTCCAAGG[A/G]TGAAAAAGAGTCAAG | 17970 |
rs31180904 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152831860 | TTATGACTACATTTT[C/T]CCAGAGCCCTGTCTT | 17970 |
rs31180905 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152831770 | GAGTCATTTAGGAAA[G/T]TCTCGTTTCTTTTGC | 17970 |
rs31180906 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152831702 | CAGGTTGGTGGCCCC[A/G]AGGAAGGAGCTCTCT | 17970 |
rs31180907 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ncf2 | Mm_Celera | 1:152831525 | TGTCATAGCGTTCCA[C/T]TTTAGGAAGCCATTT | 17970 |
rs31180908 | snp | A/G/T | 0.5 | 0 | intron-variant | Ncf2 | GRCm38.p3 | 1:152831519 | TTCCTGTGTCATAGC[A/G/T]TTCCACTTTAGGAAG | 17970 |
rs31180909 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ncf2 | Mm_Celera | 1:152831468 | GTTTTGTATGTGGGC[A/G]TTAGGGTTCTTATTG | 17970 |
rs31180910 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152831406 | AGAAGCGTGCCATGT[C/T]ACCTGACGCTGATGG | 17970 |
rs31180911 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152830945 | TCTACTGGACTGGCC[C/T]ACCTCTGTTAGTCCT | 17970 |
rs31180912 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152830910 | GAGCTGAGCCTGTGT[C/T]GAGTGGAGGCAACAG | 17970 |
rs31180913 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152830585 | TTGCAGAACTCCCAA[A/C]GGTCATCATCTGTGT | 17970 |
rs31181874 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152830546 | GAGATGCTAAGGGCA[C/T]AGAGACAGTATCTGC | 17970 |
rs31181875 | snp | A/G | 0.48 | 0.0979796 | synonymous-codon | Ncf2 | Mm_Celera | 1:152830367 | GGCTCTGGAAGGTGA[A/G]GCACACCGCGTATTG | 17970 |
rs31181876 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152830278 | CAAGCTAAGTCTCTG[A/G]CCTCAAGTGCTTCCC | 17970 |
rs31181877 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Ncf2 | Mm_Celera | 1:152830249 | GCAGTAAGATGTGGA[A/G]TTAGAGTGAGTGCCA | 17970 |
rs31181878 | snp | C/G | 0.32 | 0.24 | intron-variant | Ncf2 | Mm_Celera | 1:152830218 | TGGGTGGCAGCACCC[C/G]ACACTGGTCTTGTAG | 17970 |
rs31181879 | snp | C/T | 0.32 | 0.24 | intron-variant | Ncf2 | Mm_Celera | 1:152830055 | GGAATTTATTCTGGA[C/T]CTGCTGTCACACCAC | 17970 |
rs31181880 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ncf2 | Mm_Celera | 1:152829335 | CATATGCCCCCCAGA[C/T]ATGATAACTAAAGCT | 17970 |
rs31181881 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152829175 | AACAAAACCAAAACC[C/T]TGGTCATGAGACGCT | 17970 |
rs31181882 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152829094 | GATCAACAAAATCAA[A/G]TTTCATTTGAAAAAA | 17970 |
rs31181883 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ncf2 | Mm_Celera | 1:152828639 | AGGCCAGCCTCAGGT[A/G]CATGGTGGGTGGAGG | 17970 |
rs31182744 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152828543 | CCACCTATGTTACTC[C/T]CCTGCTCATACTTCC | 17970 |
rs31182745 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152828508 | TCTGAGGTGGTCTCT[C/T]CCCTGGTGTTCACTG | 17970 |
rs31182746 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152828445 | GTGCTGCAGTTTCTC[C/T]ACTGTGCCTTCCATT | 17970 |
rs31182747 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152828402 | AGGGGTCAATGAAGC[A/G]GAAAGGACATGGCTA | 17970 |
rs31182748 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152828312 | GTGTATGGGTAGTTT[C/T]GCAGACAGCTTCCCT | 17970 |
rs31182749 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ncf2 | Mm_Celera | 1:152828261 | AGGGACTTTGCAAAC[A/G]AGGGCAGGGCTGAGC | 17970 |
rs31182750 | snp | A/T | 0.5 | 0 | intron-variant | Ncf2 | Mm_Celera | 1:152828212 | TTCCCCAATTCTCTA[A/T]ACTAAAGAGGCTGCA | 17970 |
rs31182751 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ncf2 | Mm_Celera | 1:152828200 | TGAAGGAGCTCATTC[C/T]CCAATTCTCTAAACT | 17970 |
rs47373647 | snp | A/C/G | | | utr-variant-5-prime | Ncf2 | GRCm38.p3 | 1:152807978 | AGCGCCTACCCGGCA[A/C/G]CTCTGAGAGAGACAC | 17970 |
rs49691055 | snp | A/G | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152807974 | CTGGAGCGCCTACCC[A/G]GCAGCTCTGAGAGAG | 17970 |
rs211695886 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152823151 | CTCATCAGACAAGTT[G/T]TTTTTTGTGCAGTGA | 17970 |
rs211725195 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816048 | CCACCAGCTCCTTCT[C/T]ACAAAACAAGCACTC | 17970 |
rs211850600 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152810551 | AGGCCATCAGAGCCC[A/G]TAGAACTAGAATTTC | 17970 |
rs211854998 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802556 | TCGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 17970 |
rs211901519 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152828098 | AGGAACAAAGCAAGC[C/T]ATCTTCCTCCTCCAA | 17970 |
rs211901640 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152834486 | CTGAAGCTTTAGAGA[A/G]TATCAGAACTACCTA | 17970 |
rs211961875 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799714 | CAGATCCCAGAAAAG[A/G]GGAGGGAGCATGGAT | 17970 |
rs212057190 | in-del | -/AG | | | intron-variant | Ncf2 | Mm_Celera | 1:152825166 | TCAGAAGGTGGAGAC[-/AG]GGGATCCTCAAGCAA | 17970 |
rs212080897 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804387 | CTTGCCCGCTTACAC[C/T]TTGTTAGTCTATAAC | 17970 |
rs212094877 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152800594 | GACACCATGATTTAT[C/T]CACCATCATGGACTG | 17970 |
rs212112807 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152809808 | GTTTGTTTTGGTTTT[A/G]GTTTGTTTGTTTGTT | 17970 |
rs212124820 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819015 | CTACCCCACGTGCAT[C/T]ATTGCTTTCTGACAC | 17970 |
rs212210493 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826292 | CCATTTGCTCCTGTA[-/T]AAGAGACTCCTTTGG | 17970 |
rs212250605 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152818770 | GAAAGTTGCCAGGCA[-/G]AGGTGGTGCGCGCCT | 17970 |
rs212420593 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815530 | GGAGCCAAGAGCCTG[C/T]CTGCTCTGGGGGTGT | 17970 |
rs212422927 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152809359 | GGAGGAAAGGGTTTA[C/T]TCGGCTTACACTTCC | 17970 |
rs212453063 | snp | C/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799309 | AGACTTTGGCTGGAA[C/T]TCAGAAGAGCCCTGG | 17970 |
rs212471408 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152804896 | CTGACTCTGGAGACA[A/G]GAACTTGAACAGAAC | 17970 |
rs212530248 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820745 | CCCCTTGTGGGTGGG[A/G]CCATCTCTGGGCTGG | 17970 |
rs212549387 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152832519 | CATGGCTTGCCTCCG[C/T]GCATGTCAGGGCGTG | 17970 |
rs212606818 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827369 | CCCCGCCCCCTCACT[C/T]TTTCTCTTGTCATCT | 17970 |
rs212627883 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827026 | GCTGAGCCATCTCAC[C/T]AGCTTGAGAGACTCT | 17970 |
rs212667684 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152817173 | AGCTGGCCCAAGTCA[A/C]GTGATCTCTGTGCCT | 17970 |
rs212680730 | in-del | -/AAAAAAAAA | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813639 | AGGATAAGGGACAAG[-/AAAAAAAAA]AAAAAAAAAAAAAGG | 17970 |
rs212734379 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808456 | AGACTTCTTCATTTG[G/T]GTTTTCTTTTACCTC | 17970 |
rs212808459 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802834 | TCCAAGTTAGCATGG[G/T]TTTGTCAAGAGACAA | 17970 |
rs212838514 | in-del | -/TT | | | intron-variant | Ncf2 | Mm_Celera | 1:152804601 | TTTTTTTTCTTTTGG[-/TT]TTTGGTTTGGTTTTT | 17970 |
rs212855813 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818717 | ATGACAAGTTCTGTC[C/T]ATATATGAGCCACAT | 17970 |
rs212866156 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152808874 | GAGTTGAACATGCTC[A/G]ATTCTCTTTATTTTA | 17970 |
rs212887018 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798160 | AGCCTGGTCTACAGA[A/G]TGAGTTCCAGGACAG | 17970 |
rs212917159 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152825721 | ACTAAAAGAGAGGGT[A/G]AGAGTAAGATAAGAG | 17970 |
rs212966451 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152811278 | CTACCCAGCCCTCTC[A/G]ACAATGTCCTTAATG | 17970 |
rs213051357 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813754 | GCAAATGGCACTTTA[C/T]AAAGGTAAAGGGGAA | 17970 |
rs213133998 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812722 | aaggaaggaagaaag[A/G]aTCACAAATGGGCTT | 17970 |
rs213141018 | snp | A/G | | | synonymous-codon | Ncf2 | Mm_Celera | 1:152830454 | CTTTGTCTTGAAGAA[A/G]GGCAGTGATAACTGG | 17970 |
rs213216307 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152803610 | TAGCACAACTAGTGT[G/T]CCTCAGTGAGGCGGA | 17970 |
rs213270553 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152831380 | TTCTCAGTACACTCC[A/G]CAGCTGAGACAGAAG | 17970 |
rs213304790 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152812203 | GGGTCAGAACCAGGG[A/C]AGCACCAGTGACAAG | 17970 |
rs213411080 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152833659 | GCTGTTTATTAAACA[C/T]CCCCCTTTCCCTGAG | 17970 |
rs213509191 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819237 | CACCATAAGCTTGTT[C/T]TTCTCAGCCAATCTT | 17970 |
rs213519766 | in-del | -/CTC/CTCTC | | | intron-variant | Ncf2 | Mm_Celera | 1:152827348 | CAGTCTGTTCTCTCT[-/CTC/CTCTC]TCCCCCCCCGCCCCC | 17970 |
rs213539756 | in-del | -/GCCTACGGCT | | | intron-variant | Ncf2 | Mm_Celera | 1:152834348 | AGAAGTGCACAGCAA[-/GCCTACGGCT]GCCTTCACTAGACTG | 17970 |
rs213600044 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152811623 | GTCTGGAAGGGCATC[A/G]GCCAATGCACTATTC | 17970 |
rs213606233 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818070 | GAGTCCCTGGGGACG[C/T]GTGGCCCATGGCCCG | 17970 |
rs213638454 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152829876 | GTAGACCAGGCTGGC[C/G]TCGAACTCAGAAATC | 17970 |
rs213665144 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152817238 | ATGCGTGTAGCTTAG[A/G]GGTGAAAAAGTGTTT | 17970 |
rs213710902 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152835348 | ATGCGTGGCTTTCTC[C/T]TGTCCTTGACTTTAC | 17970 |
rs213740655 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152833966 | CTGGGGATGCAGCAG[A/G]GGTGGATGATGGGGT | 17970 |
rs213777474 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152806332 | AGAGGAGGAAGATCA[A/C]AACATTGCTTATAAA | 17970 |
rs213990004 | snp | A/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799774 | ACATGCAGAATGACC[A/T]CATGCTTTCAGCTGC | 17970 |
rs214042421 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152821863 | TATGTGCAGCTTCTC[A/G]GGGATGTGCAGCCTA | 17970 |
rs214075754 | in-del | -/TCCTCCTCCTTCTCT | | | intron-variant | Ncf2 | Mm_Celera | 1:152806933 | ATAGCACCTTCCTCC[-/TCCTCCTCCTTCTCT]TCCTCCTCCTCCTCC | 17970 |
rs214220523 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815560 | TGGCTGTTTCTCGGC[A/C]GATGTCTTAGGAAGC | 17970 |
rs214220626 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822521 | GAGGTTAAAGCCAAC[C/T]GCTTCCAGTAGGCAA | 17970 |
rs214251562 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152805822 | AAGAGAATTAGCCAG[A/G]GATGGCCAGAAGACT | 17970 |
rs214270717 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152829316 | CCGCTTGTGCACTGC[C/G]GCACATATGCCCCCC | 17970 |
rs214316567 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798567 | TTTTCCCTCGGGAGG[A/G]TAAACATTTGAGGCC | 17970 |
rs214338914 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152828362 | GGAGACTCTCTCTAG[A/G]AGTGGAGAAGTAACC | 17970 |
rs214356657 | snp | A/C | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152836988 | ATAAATCCTCTACAC[A/C]CCGATCTGCTTGGAG | 17970 |
rs214401003 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799137 | GGTCCTTCCTGGTAC[A/G]TGGGTACAGTCCCAA | 17970 |
rs214483964 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152810431 | CTAACTATATCACTA[C/T]TATTTTATTTTTATT | 17970 |
rs214641067 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152805196 | GTGAGTGCAGGACAC[A/C]GGGTGGACCTGCCTA | 17970 |
rs214663981 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804873 | TGTGATATGACTGAA[C/T]CCTCACGCTGACTCT | 17970 |
rs214686149 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809020 | TGTTCAACATGACCA[C/G]CAGGCCTCTTGATTG | 17970 |
rs214739296 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820689 | CTTCCATGAGATCCA[A/G]CTATAAGGCATTTTC | 17970 |
rs214775934 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152827884 | GGCGTGGTGGTGCAC[A/G]CCTTTAATCCCAGCA | 17970 |
rs214780475 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152810873 | CAAGTCTTGCCTCTC[C/T]CTGGCAATACTCTGA | 17970 |
rs214801073 | in-del | -/TTTCTCGGCAGA | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815551 | CTGGGGGTGTGGCTG[-/TTTCTCGGCAGA]TGTCTTAGGAAGCCT | 17970 |
rs214898252 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802786 | TTATGGTTCTACAAG[A/T]TCATTATAAGTTTAA | 17970 |
rs214930538 | in-del | -/A | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799451 | CTGATTCTCCCCCCC[-/A]CCCCCCAAGACAGGG | 17970 |
rs215038999 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827396 | TCTTCCCCTTCTTCA[-/T]TTTTTCCTGAATGTT | 17970 |
rs215097167 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152826234 | TGCAGGGGATAGGGT[A/G]CCAGGGCTTGGAGCC | 17970 |
rs215100051 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804377 | AGAAAATTACCTTGC[C/T]CGCTTACACTTTGTT | 17970 |
rs215150189 | snp | A/G | | | missense | Ncf2 | Mm_Celera | 1:152833867 | CTTGGCCTCCCCTAC[A/G]GCCAGCTTCGGAACA | 17970 |
rs215213515 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825029 | CCAGAAGAAATACAG[A/T]TGCCATGGCCAAGTG | 17970 |
rs215344247 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818663 | TGTAGTAAATAGTAA[C/T]GGGCAGCCAAGTTTG | 17970 |
rs215367922 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809305 | TCTTAGTCAGGGTTT[C/G]TATTCCTGCACAAAC | 17970 |
rs215439555 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826984 | TTGAACTCAGGACCT[C/T]TGGAAGAGCAGTCGG | 17970 |
rs215495813 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813117 | CCCTCAGATTTTTTT[A/T]TAAAAGATTTATTTA | 17970 |
rs215585381 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152817190 | TGATCTCTGTGCCTC[A/G]AGCCGCATGCTGTCT | 17970 |
rs215712161 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806299 | TGCCGCTGCCGCTGC[C/T]GCTAAGGAGGAGGAG | 17970 |
rs215713288 | snp | A/T | | | utr-variant-5-prime, intron-variant | Ncf2 | Mm_Celera | 1:152807559 | GGCCGGAGTACTGGG[A/T]GTTCAGACAAGCCTG | 17970 |
rs215751562 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822758 | CATGGAGAAATCATG[C/T]TGCTACTGAGCAAGA | 17970 |
rs215751925 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806073 | CTTGGGAAAGAAGAC[A/G]AGGTCATGGGCTGCA | 17970 |
rs215784261 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152831442 | CAGCATGGTCGAAAA[-/G]ATGGCAAAGGGTTTT | 17970 |
rs215844790 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152830332 | TGAATGGTGGGCTCA[C/G]TCTTCTGTGTACCCC | 17970 |
rs215891079 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152829639 | GTTTTTTGTATGTGA[C/G]TAGACTGTAGCTGTC | 17970 |
rs215931323 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152823292 | AAGGCTCAGGGCCAT[A/G]GCAGATGAGGGGGAC | 17970 |
rs215993295 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152802121 | TGGGGAGGGAGGGTG[C/G]TGGTGGCAAAAGCTG | 17970 |
rs216016498 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152805151 | GGAGTGGCCCTTGCA[G/T]CTGGGACACAAGGAG | 17970 |
rs216018425 | snp | A/C | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799412 | CATGGCAGAACCTAC[A/C]GCTCCCTCTCCTGAC | 17970 |
rs216045967 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152831758 | CAGCTGTTTTCAGAG[C/T]CATTTAGGAAATTCT | 17970 |
rs216097422 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799724 | AAAAGAGGAGGGAGC[A/G]TGGATGCTTCACTTA | 17970 |
rs216142888 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152808387 | CCCATGGGTGGGGCT[A/C]TGCTCTTTATGAGAT | 17970 |
rs216157045 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813702 | AGAGGGGCAAAGGAC[C/T]GCCTCTGGATAGAGA | 17970 |
rs216158684 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819196 | TGACCTTTGTGTGCT[G/T]TGTGCCCAGACCACA | 17970 |
rs216388875 | in-del | -/AG | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813623 | ACAAAGACTGGAGAC[-/AG]AGGATAAGGGACAAG | 17970 |
rs216425293 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152811550 | GTTTACAGTTGATGG[C/T]AAAATTTAAACAATG | 17970 |
rs216445528 | snp | A/C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152821774 | CTTCCATCCTGTATT[A/C/T]GAAACTAAGAAGCCA | 17970 |
rs216502303 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820786 | TTCTATAAGAAAGCA[A/G]GCTGAGCAAGCCAGG | 17970 |
rs216504270 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152827782 | GCGTTTTTTCTAAAG[A/C]AGGGGAAAGACTCAA | 17970 |
rs216505118 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152836500 | GGTTCCAGAAGCTTA[A/G]AGCAAATTTATATGT | 17970 |
rs216510755 | in-del | -/CT | | | intron-variant | Ncf2 | Mm_Celera | 1:152826820 | TACATTAAAGAGAGA[-/CT]CTTTTTTCAAAATAT | 17970 |
rs216553318 | in-del | -/ACCC | | | intron-variant | Ncf2 | Mm_Celera | 1:152819164 | GCTGGGGTGGGTGTG[-/ACCC]TTTAATCGCCTGGTG | 17970 |
rs216555449 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152835281 | AGACAAAGGAAAACA[C/T]CAACTCTTAGCTAAT | 17970 |
rs216586463 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152803754 | GGGGGTTTCCAGTTC[C/T]GCGCTGGACAGTATC | 17970 |
rs216679073 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152830009 | GACAGGAGGATTGCT[A/G]GAAGTACAGGCCAGC | 17970 |
rs216746664 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152811062 | GATGGATCGGGCTTT[C/G]TTCTGTAGTCTTGGT | 17970 |
rs216781045 | in-del | -/TCTGCTTGTTGTCCTCCAGG | | | intron-variant | Ncf2 | Mm_Celera | 1:152803676 | GTTATAGAGTTTTGC[-/TCTGCTTGTTGTCCTCCAGG]TCACCATGTCCCTCC | 17970 |
rs216838142 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152808588 | CTGCTCAAAGAACAA[C/G]TCTGATCAACAAGGC | 17970 |
rs216906741 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152802237 | GCTGTCCAGGTGAGA[A/G]GCCCAGAGATCCTTA | 17970 |
rs216991308 | in-del | -/TTTGTTTC | | | intron-variant | Ncf2 | Mm_Celera | 1:152822046 | GAGTGTTTTTTTTTT[-/TTTGTTTC]TTCTTTATTTGGAGA | 17970 |
rs217044298 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152804132 | TAATTTCTTGTACCC[A/C]TTTTTGCCCTCAGCT | 17970 |
rs217052578 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152826211 | TCCATGGGTTCAGGC[A/G]TGTGAGTTGCAGGGG | 17970 |
rs217110658 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816658 | CTGCTTTGAGACTCT[G/T]CCAGAGAGAAGCAGG | 17970 |
rs217223469 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152802113 | GAGTTGGGTGGGGAG[A/G]GAGGGTGCTGGTGGC | 17970 |
rs217288987 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152810281 | CATTTTTCTGTCACC[A/G]GGCCTCTCATCTCAT | 17970 |
rs217326638 | in-del | -/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152836589 | GCAGATTGAATCAGG[-/T]TCCCATGAAGCACAC | 17970 |
rs217342702 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152829940 | GATTAAAGGCATGTG[C/T]CACCACCACCCAGCG | 17970 |
rs217354899 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152817123 | GGCAGGGATGGCCCG[A/C]GAGGGAAGCACAAAG | 17970 |
rs217382862 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815427 | CTAGACTGTGTGTGT[A/G]TTGGTAGCAGAAGGC | 17970 |
rs217384312 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806783 | ACAATACTCTCTCCG[A/T]AATGTAGAGTGCGGA | 17970 |
rs217409985 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152834569 | TTTGTGCTATGGAAA[A/G]GGGGTGAATTCAATG | 17970 |
rs217427721 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152824859 | CAATCTGAGTAAGCT[A/G]GACCTGGCAGAATCA | 17970 |
rs217457597 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815537 | AGAGCCTGCCTGCTC[C/T]GGGGGTGTGGCTGTT | 17970 |
rs217465485 | snp | C/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798844 | TCTCCTCCATCCCAA[C/T]CCTGACACAGCAAGG | 17970 |
rs217472160 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152830280 | AGCTAAGTCTCTGGC[C/T]TCAAGTGCTTCCCCA | 17970 |
rs217575740 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806316 | CTAAGGAGGAGGAGG[A/T]AGAGGAGGAAGATCA | 17970 |
rs217606781 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152809879 | GGCCAGCATTTTACC[C/T]ACAGAACGTCTCCCC | 17970 |
rs217615238 | in-del | -/AAAG | | | utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152837569 | AAAAAACAAAAAAAA[-/AAAG]AAAGAAAAAAGAAAA | 17970 |
rs217622501 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152835537 | AACCTAGGGATTACA[G/T]GGTAACATGGGCAGG | 17970 |
rs217656032 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152810002 | AAGGTACTGGATAGG[C/T]TCAGACTCTTCCGGT | 17970 |
rs217723811 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152829100 | CAAAATCAAATTTCA[C/T]TTGAAAAAAAAAATG | 17970 |
rs217736636 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152833022 | TTCAGACCATAAACA[C/T]ACACAAAACAGGGCC | 17970 |
rs217761938 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152805294 | GATCCTCACATACAC[C/T]AAGTGTTGCTATGTA | 17970 |
rs217773100 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804986 | AGTGGGGAGTATTGA[C/T]TAAACACACTGTCCC | 17970 |
rs217928710 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809547 | ATGACACCACCCACA[A/G]GGGCCTTTCCCCCTT | 17970 |
rs217975934 | in-del | -/A | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812909 | CTCAGATTTTTTTAA[-/A]GGTTCTTTTTCTTTT | 17970 |
rs218009519 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798227 | AAAAAAAAAAAAAAA[A/G]GTGCCTCGGGCCTGT | 17970 |
rs218080504 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813865 | TGGTAGTCAGCCTCA[G/T]GAGGAGGAAGTGGCC | 17970 |
rs218096410 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152835463 | ACTTTCCAGAGAGAA[-/G]GGGAGGTCCATTCTG | 17970 |
rs218164642 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152820321 | TGGAAATGGCAGTCC[C/T]GTCACCCAGGTGCGT | 17970 |
rs218218494 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152832883 | CTCCTAGGCCTTTGA[C/T]TGATTTTAGCAAAAG | 17970 |
rs218288622 | in-del | -/AAAAAAA/AAAAAAAA | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798209 | CCTTATCTCGAAAAC[-/AAAAAAA/AAAAAAAA]CAAAAAAAAAAAAAA | 17970 |
rs218314858 | in-del | -/GCTGCC | | | intron-variant | Ncf2 | Mm_Celera | 1:152806282 | GGCTAGGATGCTGCT[-/GCTGCC]GCTGCCGCTGCTGCT | 17970 |
rs218342946 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152827234 | AGGCCCAGGTGGGCG[C/G]CAGGCTTTTGGTTTC | 17970 |
rs218356676 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814556 | AGGCAAACATCATAC[C/T]ATCTACATCTTGATC | 17970 |
rs218372619 | in-del | -/AA | | | intron-variant | Ncf2 | Mm_Celera | 1:152829020 | TGTGTGTGTGTGTGT[-/AA]GTAAGTAAAAGGCCC | 17970 |
rs218372825 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152808685 | CACCAAGGGTATGGG[A/G]TAGGGCATTTCAGCA | 17970 |
rs218445591 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152821360 | ACCGCTTATGTCTGA[C/T]ATAACTCAGTAGTTA | 17970 |
rs218525034 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809090 | GGTGGGGGTGGCTAC[A/G]TATGTCATGACGCAC | 17970 |
rs218553391 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819510 | TCATGTCCTCTAGAG[A/T]TCCTATGTAGTCACC | 17970 |
rs218649165 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814093 | TGGGGCTATGGATGG[A/G]TATGAGCCACCATGT | 17970 |
rs218675314 | snp | A/C | | | synonymous-codon | Ncf2 | Mm_Celera | 1:152831664 | TCCTAATTCTAGCCC[A/C]CCAGGAAGACTCCAG | 17970 |
rs218689507 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812396 | CCTTAGAGGATAAGA[G/T]CACTGGCTGCTCTTC | 17970 |
rs218723972 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819547 | CTTTACTTAGCTTAC[-/T]TTATGCTTTATTGTG | 17970 |
rs218735083 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152801758 | TCATGATTTTAAAGG[C/T]TACCTGTGGCTATCT | 17970 |
rs218740954 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818190 | CCCTGAGGACAGGGG[C/T]TATCTCCCTCCATAA | 17970 |
rs218772555 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819271 | aacccatctttcctt[C/T]cttcctttctttctt | 17970 |
rs218801170 | snp | C/T | | | utr-variant-5-prime, intron-variant | Ncf2 | Mm_Celera | 1:152807659 | AAGTACAGGACCAGG[C/T]CCAGACCTGCTGAGG | 17970 |
rs218997100 | in-del | -/GGA | | | intron-variant | Ncf2 | Mm_Celera | 1:152822595 | TTTGCGGGGGGGGGG[-/GGA]GTGTCTCCTGGATAC | 17970 |
rs219035645 | in-del | -/TA | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815427 | TAGACTGTGTGTGTG[-/TA]TTGGTAGCAGAAGGC | 17970 |
rs219038340 | in-del | -/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152821424 | AAGGGAACTATGTCA[-/C]CAGTCAGCATTCCCT | 17970 |
rs219053009 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813059 | GAACTCAGGACCTTC[A/G]GAAGAGCAGTCAGTG | 17970 |
rs219087315 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152809160 | CCATTTTGACCTGGA[-/T]TCCAGTGACCGACCC | 17970 |
rs219108824 | in-del | -/TT | | | intron-variant | Ncf2 | Mm_Celera | 1:152825953 | ACAGGTGAGACTGGC[-/TT]TCTCTGGGAAGTAGA | 17970 |
rs219279922 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814208 | GCCTTTGTTACGTGA[A/G]TCCTTGAGATCTGAG | 17970 |
rs219288607 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152835738 | ATCAAAATGAATTCT[A/C]GCAGAGCTCAGATAA | 17970 |
rs219291565 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152817350 | GAGGAAAGGAGAGAG[A/G]AGGGGAGGGAGATTT | 17970 |
rs219330094 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152815959 | TGAGTTTAACACCAG[C/T]TTTGGATACATCAGA | 17970 |
rs219339956 | snp | C/G | | | utr-variant-3-prime | Ncf2 | Mm_Celera | 1:152836300 | TGGAGGAGGGGGAGA[C/G]AAATTTTCTGCAAAG | 17970 |
rs219412943 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152816907 | AGAAGGTCAAACAGA[A/G]CAGGAGGGCTTCTTG | 17970 |
rs219416756 | in-del | -/AGG | | | intron-variant | Ncf2 | Mm_Celera | 1:152806304 | CTGCCGCTGCTGCTA[-/AGG]AGGAGGAGGAAGAGG | 17970 |
rs219417287 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152810715 | ATCACTTATTTTACA[A/G]AGGAAAACAAGGAGG | 17970 |
rs219417834 | in-del | -/ACAAAACAAAACAAAACAAAACAAAACAAA | | | intron-variant | Ncf2 | Mm_Celera | 1:152803430 | TAGATGACTTCTGAC[lengthTooLong]ACAAAACAAAACAAA | 17970 |
rs219469820 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816221 | GCTCAGCCAACTCTG[C/T]AGGGAGCAAGACACG | 17970 |
rs219523888 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152837508 | TCAGACCTTTcaaaa[A/G]caaaacaaaacaaaa | 17970 |
rs219576881 | snp | A/G | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800374 | GGTGTGAAGCTTTGT[A/G]TTTCGAGCTTGACAG | 17970 |
rs219583418 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152833527 | TTCTGTCTCAGTGTG[C/T]TGGATTGGAGCCCTC | 17970 |
rs219606717 | in-del | -/AC | | | intron-variant | Ncf2 | Mm_Celera | 1:152809050 | CTTAGGTGTGTGTGT[-/AC]GTGTACATGTGCGTG | 17970 |
rs219652167 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809887 | TTTTACCTACAGAAC[A/G]TCTCCCCAGCCTCCA | 17970 |
rs219655205 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152832570 | TTTAAATGGAAACAA[C/T]CCGTCAGCTACTTAC | 17970 |
rs219660760 | snp | C/T | | | synonymous-codon | Ncf2 | Mm_Celera | 1:152834090 | GCGTCGGGACAGCCA[C/T]GAGCTTCTGCTCCTG | 17970 |
rs219737879 | in-del | -/TATT | | | intron-variant | Ncf2 | Mm_Celera | 1:152802766 | TGAATAAATAGTCAC[-/TATT]TATTTTATGGTTCTA | 17970 |
rs219741004 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815331 | AGAGGATTGGCCCTG[A/T]CCACCAGGGGCAGCA | 17970 |
rs219742060 | snp | C/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799935 | CTCTCTGTAATCCTC[C/T]ACCCTCTACGTGTCA | 17970 |
rs219768585 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798851 | CATCCCAATCCTGAC[A/G]CAGCAAGGACAGAAA | 17970 |
rs219796471 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814697 | GTCATATTCTCTATT[G/T]GTATGGTCTATGGGG | 17970 |
rs219800317 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820897 | ACTTCCTGTGGTGAT[A/G]CACAGCAGTGTGGAA | 17970 |
rs219811344 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799559 | GCTGGGATTAAAGGC[A/G]TGCACAACTACTGCC | 17970 |
rs219890538 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799509 | GACCAGGCTGGTCTC[A/G]AACTCAGAAATCCAC | 17970 |
rs219995679 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819607 | GCTGTGCTTAAATAT[G/T]CCTGAAATAAACTAC | 17970 |
rs220035108 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152820587 | CTGTGCATGCTGACT[A/C]TCTTTCTACCTTGTC | 17970 |
rs220142526 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815413 | TGAGCTCTGGGACTC[A/T]AGACTGTGTGTGTGT | 17970 |
rs220150737 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152834781 | ATTTATTTGTGGCTC[-/A]ATATCATTTCCCAAT | 17970 |
rs220178172 | snp | C/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798239 | AAAAGTGCCTCGGGC[C/G]TGTAAACCCTGGCCA | 17970 |
rs220339551 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152823058 | TGAACCCACTACTAT[C/T]ACTTGGCTAAAAGGG | 17970 |
rs220344926 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152802597 | GGATTAAAGGTGTGC[A/G]CCACCACGCCCGGCT | 17970 |
rs220360794 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815606 | GAGGGCACTTGGAAG[A/G]GGGCCAGCCAGAAGG | 17970 |
rs220403798 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825852 | AAACAGAGCCTGGCA[G/T]CAGCACGCTCACCTT | 17970 |
rs220408638 | in-del | -/AGACCCAGAGCCTG | | | utr-variant-5-prime, intron-variant | Ncf2 | Mm_Celera | 1:152807586 | CTGGGTTACATCCCT[-/AGACCCAGAGCCTG]AGACCCAGAGCCTGA | 17970 |
rs220465717 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813546 | CAGGACACACCAAGA[C/T]CAAGTTCTCAACACA | 17970 |
rs220523589 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152803881 | GTAGATGGTTGGTAA[C/T]GTCAACCACCCTTAG | 17970 |
rs220560842 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818812 | ACTCGGGAGGCAGAG[G/T]CAGGCGGATTTCTGA | 17970 |
rs220667717 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813930 | AACTGAACCCAAGGG[A/T]TTTTAGCAGGGGGAG | 17970 |
rs220717160 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825276 | GGATGATACTTAGAT[G/T]AACCTGCAACCTCTA | 17970 |
rs220730718 | in-del | -/AGAAGC | | | intron-variant | Ncf2 | Mm_Celera | 1:152816664 | GAGACTCTTCCAGAG[-/AGAAGC]AGAAGCAGGGTGGTT | 17970 |
rs220778034 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152817544 | GGAGAGTAGTCACAG[A/C]AATTTGCATATTTTA | 17970 |
rs220781317 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152815818 | AGCTCAGTTGGTAGC[A/G]CTTGCCTAGCTTGCA | 17970 |
rs220840789 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152824369 | CCTGTGCCCTGGATT[A/G]CATGGGGCCTGGTGG | 17970 |
rs220845219 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825954 | CAGGTGAGACTGGCT[C/T]TCTCTGGGAAGTAGA | 17970 |
rs220845292 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152818348 | CAAACTGTCACTCAC[C/G]CTGCCGAGGGCCGCT | 17970 |
rs220855578 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819756 | TCCCGCCCCCACATG[C/T]CACACCAACCTTCTC | 17970 |
rs220874746 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152802543 | GACCAGGCTGGCCTC[C/G]AACTCAGAAATCCGC | 17970 |
rs220876562 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152801243 | GGTGGGCTCTGGTTG[C/T]ACAGGCCTGGAATTC | 17970 |
rs220923864 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809171 | ctggatccagtgacc[A/G]accccaaatctctga | 17970 |
rs220976460 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152803139 | GTATTAGTTTAGGAG[A/T]ATAAAATCATTATCA | 17970 |
rs221001959 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152819040 | TGACACAGCACACCA[C/G]TGTGTTGTACCCGTG | 17970 |
rs221008411 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152801781 | GGCTATCTAAAGTCA[A/C]GTAGAATCTAGATCA | 17970 |
rs221077710 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152805690 | GTGGGGTAGAGACCC[A/G]TAATTAATATTTACC | 17970 |
rs221116771 | snp | A/C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152823471 | GTTCATGAGCCATCC[A/C/T]TAACTGAAGAGCTAT | 17970 |
rs221147887 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152805416 | GTTCCCAGGCTTGGG[A/G]TCTGAGACAGGATCA | 17970 |
rs221183352 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152809787 | GATGTGACTCCACCC[C/T]TGTTGGTTTGTTTTG | 17970 |
rs221189760 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802804 | ATTATAAGTTTAAAG[C/T]AATAGTTTTTATGTT | 17970 |
rs221203113 | in-del | -/AAAAA | | | utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152837561 | AAAAAACAAAAAAAC[-/AAAAA]AAAAAAAAAAAGAAA | 17970 |
rs221221073 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152829973 | GGCTCACATTTCTGA[C/T]CCCCACCTTTGAGAG | 17970 |
rs221267404 | snp | C/G | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800438 | GATCGTCTGCCTTAG[C/G]TTAACTGAGGTAGAG | 17970 |
rs221315502 | in-del | -/AAAACCAAAAA | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798205 | AGAAACCTTATCTCG[-/AAAACCAAAAA]AAAAAAAAAAAAGTG | 17970 |
rs221350379 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819935 | TCTTTCTTCTGAATG[C/T]ATTTCTCTTTTGTAC | 17970 |
rs221387720 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152801778 | TGTGGCTATCTAAAG[C/T]CACGTAGAATCTAGA | 17970 |
rs221715911 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822115 | AGAATGGGCACATGT[G/T]GGTATGTGGCCGTAG | 17970 |
rs221723749 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820537 | GATGTTCAGTCACCC[C/G]CTTCCCTGGTGCCAT | 17970 |
rs221776508 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152830151 | GAAGGGGAACTCCTG[-/T]GTGCTACAGAACACA | 17970 |
rs221833344 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152800940 | CTGAAAAGGATGACT[A/G]TAGCCCCAAAGAGAG | 17970 |
rs221873113 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152803011 | GAATGTTTTCCCTGA[A/G]TGTAAATTTGTTCCA | 17970 |
rs221886575 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806993 | CTTCTTCTCAGTCCT[C/T]CTACCTTACAAACTC | 17970 |
rs221956090 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152826426 | GTGAAGTAGATTAAG[A/G]AGACCTCAGGCTTGG | 17970 |
rs221988177 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152830062 | ATTCTGGACCTGCTG[C/T]CACACCACAGGCTAC | 17970 |
rs222093668 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152802904 | GTAAACTAGTTCATC[A/G]CTTATTTTCTGTCCT | 17970 |
rs222105511 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802574 | CTGCCTCTGCCTCCC[G/T]AGTGCTGGGATTAAA | 17970 |
rs222120792 | in-del | -/G | | | utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152837576 | AAAAAAAAAAAGAAA[-/G]AAAGAAAAAAAATCC | 17970 |
rs222195161 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822206 | GTCTGATGTGGATGC[C/T]GAGAACCAAACTCTA | 17970 |
rs222234625 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152804606 | TTTTCTTTTGGTTTG[C/G]TTTGGTTTTTCAAGA | 17970 |
rs222264137 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152807218 | AACTTTGACATTACC[A/G]GGGCAGTAAGTAAAG | 17970 |
rs222358954 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152821776 | TCCATCCTGTATTTG[-/A]AACTAAGAAGCCACA | 17970 |
rs222398858 | in-del | -/CT | | | intron-variant | Ncf2 | Mm_Celera | 1:152832195 | GTGGGAAAATGATGA[-/CT]CTTTGTTCCTGGTGA | 17970 |
rs222406970 | in-del | -/ACTCTGTGGAGTTCCC | | | intron-variant | Ncf2 | Mm_Celera | 1:152809125 | GTCAATCAAAGGACG[-/ACTCTGTGGAGTTCCC]TCCTTCCATTTTGAC | 17970 |
rs222617815 | in-del | -/TGG | | | intron-variant | Ncf2 | Mm_Celera | 1:152802460 | TGTTTTGTTTTGTTT[-/TGG]TTTGGTTTTGGTTTT | 17970 |
rs222634028 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152828626 | AGGATAAGAGTTGAG[A/G]CCAGCCTCAGGTGCA | 17970 |
rs222765684 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152822870 | AGCCTGGTGAACTGA[A/G]GTGAAGATTGGGGTT | 17970 |
rs222801373 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804959 | AGAGTGGCAGAAAGG[C/T]CGTCGGCTAGCAGTG | 17970 |
rs222840078 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152804733 | GCTGGGATTAAAGGC[A/G]TGCGACACCACGCTC | 17970 |
rs222919833 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152809481 | TACTGGCTTGCTTCC[A/C]TTGGCTTGCTCAGCC | 17970 |
rs222966194 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152811719 | AGGCTATTTACTGTC[G/T]TAAGTAAAAAGAAAA | 17970 |
rs222983472 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152825204 | CTACCCATAGTAGTC[A/C]GCTCGGAGTTTGATT | 17970 |
rs222987657 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152801287 | TGTGGCGAATTCAAG[A/C]CAGACCTAGGCTGCA | 17970 |
rs222991004 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806526 | TTTTATATTAAGACA[G/T]AATCTTACTAGATTG | 17970 |
rs223036058 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813293 | TGGTTGCTCTTAGCA[A/G]CAGCTGAGCACCCCA | 17970 |
rs223158409 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152830158 | AACTCCTGTGTGCTA[C/T]AGAACACACTCACAT | 17970 |
rs223167978 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152832999 | TGCTGTGCTAACATA[G/T]TGTGCATTTCAGACC | 17970 |
rs223264063 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152805179 | GAGGGATAGAGATCT[C/T]GGTGAGTGCAGGACA | 17970 |
rs223291871 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152824601 | GAAAAAGGACATAGT[A/G]GGGGCTCACTGAGAG | 17970 |
rs223327489 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806116 | TTCAGGCCAACTGGG[A/G]GAAGCTAGATGAGCT | 17970 |
rs223343096 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808922 | GGAGACCTGGTTATC[C/T]TAAAACACAGTCTAC | 17970 |
rs223349486 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814735 | CCATTCAAACTATCA[C/T]ACCCATATGTGTTGA | 17970 |
rs223410683 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814203 | GCTTGGCCTTTGTTA[C/T]GTGAGTCCTTGAGAT | 17970 |
rs223419302 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152827517 | TACGTCTGACTTGAC[A/G]GCAGTAAGGATGTAA | 17970 |
rs223524120 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809208 | ACAGCAAGTGCCTTT[A/G]TCTGCTGAACTCGAT | 17970 |
rs223600197 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152811162 | AGTAGTAAGCAAGAG[A/G]CTTTTCTGGGAAGGG | 17970 |
rs223657407 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152835982 | TTTTAGTAATCAGTG[-/T]ATATTTTGCTTTTTA | 17970 |
rs223709619 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813507 | TTTAAGATTATTTTA[C/T]ATATGGAAGGACCAG | 17970 |
rs223849895 | snp | A/C | | | missense | Ncf2 | Mm_Celera | 1:152808123 | TGGAGGCCTTCAGCG[A/C]GGTGCAGGACCCCCA | 17970 |
rs223903718 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152830790 | GAGGCCTAGCCTGTT[G/T]CTCTCACCCTTCACA | 17970 |
rs224011506 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806803 | TAGAGTGCGGAGTGG[A/G]CTGTCGCACAGTAGG | 17970 |
rs224053949 | in-del | -/A | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815618 | AAGGGGGCCAGCCAG[-/A]AGGGCTGGACCTCTT | 17970 |
rs224195983 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820908 | GATACACAGCAGTGT[-/G]GGAAGTGTAAGCTGA | 17970 |
rs224298159 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152832269 | ACGACCACCTGATGA[C/G]CAAAGACTGCTTTGG | 17970 |
rs224406522 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152811741 | AAAAGAAAAACCAAA[A/T]CAAACAAAACACCCA | 17970 |
rs224455461 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152829507 | GACCTGCAATTTGTT[A/T]ACGCCAAAGCTATAA | 17970 |
rs224468429 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152835658 | ATGTACTAAACCTAT[C/T]ACTAGCTCCAATTTT | 17970 |
rs224537984 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152832415 | GGTGGCTCCACAGTC[-/A]AAGACGCTTGCTGCA | 17970 |
rs224543830 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152828861 | AGCCGTCTGTCCACA[C/T]AGGATCGGCTGTCAG | 17970 |
rs224547160 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152831870 | ATTTTTCCAGAGCCC[C/T]GTCTTGCTTGCACCA | 17970 |
rs224551745 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152829878 | AGACCAGGCTGGCGT[C/T]GAACTCAGAAATCTG | 17970 |
rs224623514 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812928 | TCTTTTTCTTTTTTT[A/T]AAGATTTATTTATTT | 17970 |
rs224656787 | snp | A/G | | | synonymous-codon | Ncf2 | Mm_Celera | 1:152810992 | AATGCTCTACTACAG[A/G]ATGGAGAAGTAAGTG | 17970 |
rs224663563 | in-del | -/AAACAAAACAAAACA | | | intron-variant | Ncf2 | Mm_Celera | 1:152803429 | TAGATGACTTCTGAC[-/AAACAAAACAAAACA]ACAAAACAAAACAAA | 17970 |
rs224689551 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152817136 | CGCGAGGGAAGCACA[A/C]AGGTCTAGCTGTTGT | 17970 |
rs224730747 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152816433 | AGGGGTCCAGGAAGC[C/G]TACCTTCTCATTCTT | 17970 |
rs224747641 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152808264 | AAACCTCATCCCCCA[A/G]AGCCGGAAAGGAACA | 17970 |
rs224762882 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152803528 | GCCTGAACCAATTAG[-/A]ACACTTGCCAGGATG | 17970 |
rs224806886 | snp | G/T | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152807330 | CAGACAGAGCGATGG[G/T]AATTGCTGTCATGTC | 17970 |
rs224867796 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152834848 | GTAAGGTTTATTATG[C/T]AAGGCAATTTAAAGC | 17970 |
rs224870597 | in-del | -/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152806613 | GGTGGCAGGCCTCCG[-/C]CATCAGGCTAGACTC | 17970 |
rs224937136 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152810657 | ATAGGTCCTCTGGAC[A/G]TGCAGCAAGCACTCT | 17970 |
rs224990352 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152815757 | GGGGGGTGAGGAGGG[A/C]AGCCAGGCAAATGAT | 17970 |
rs224998137 | snp | A/C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816094 | TTTTCTAAAACAAAA[A/C/T]AAAACAAAACATTGT | 17970 |
rs225135733 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152801451 | ATCTTCAGTACCGGT[-/G]GGGGTGGGGTGGGGT | 17970 |
rs225215410 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152809377 | GGCTTACACTTCCAT[A/C]CTGCTGTTCATCACC | 17970 |
rs225236617 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152810033 | CAGCAAGCAGATGGT[A/G]CAGAGCACGGCCCCC | 17970 |
rs225266502 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825371 | CACACACACACACAC[-/T]ACACACACACACACA | 17970 |
rs225288040 | in-del | -/ACTATGCATACAAC | | | intron-variant | Ncf2 | Mm_Celera | 1:152816749 | ATCAGAAAGGTGGGA[-/ACTATGCATACAAC]ACTTAGAGAAGAATA | 17970 |
rs225314030 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152833422 | CTCTTAGAATATGGA[A/C]TATCAATGAAAGGGT | 17970 |
rs225344028 | snp | C/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798367 | ACGAATGTGCTAGAT[C/G]ACATGTGGGCAGGAG | 17970 |
rs225389017 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814125 | AGTGCTTGGAATCAA[A/G]CCGCAGTCTTCAGTG | 17970 |
rs225462278 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152819785 | TCGCCTCCTACAGAG[A/G]GCCACTTGCTTTCCT | 17970 |
rs225511289 | in-del | -/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152833460 | TTGCTACCTGACTCT[-/C]CCATCTACACGTCAT | 17970 |
rs225544182 | in-del | -/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152808241 | ATTATAGCCTTTCCG[-/C]CCTCTGGAAACCTCA | 17970 |
rs225634510 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152828764 | TTCCATTCTGAGCAG[C/T]GTGATGAAACAATCC | 17970 |
rs225655318 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152810064 | ATCCAGCCTCCGCCT[G/T]GAGGGAGGAATGCCT | 17970 |
rs225667861 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822896 | GGGTTGTCAGATCTG[C/T]CCAGGGGTGCAATAG | 17970 |
rs225712045 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152834410 | AGCTACAACAAGAAA[C/T]AGGACTTCCTGGCAA | 17970 |
rs225842396 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152821387 | GTTAGAATAAGTGTT[C/G]GCTATCCCCTCAATC | 17970 |
rs225917469 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152809123 | GTGTCAATCAAAGGA[A/C]GACTCTGTGGAGTTC | 17970 |
rs225945868 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819995 | TCCAGATCCTGAGTC[C/T]TTGGGCCTGATGAGA | 17970 |
rs225950204 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813720 | CTCTGGATAGAGAGG[A/G]GATGGATGTGGCCCA | 17970 |
rs225981202 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152815856 | AGCTTAGCTCACTTG[A/T]TTCCCCCATCATACA | 17970 |
rs225981709 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814653 | CCCACAGTGACCCTC[G/T]TCCTCTAACAAGCCC | 17970 |
rs226026534 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818278 | CATCTCTGGCCTCTC[C/T]CCTCTAGATGGCCAG | 17970 |
rs226036937 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152832108 | GCAGAGCAGAGCCCC[C/T]AGGGCTTGAACAAAG | 17970 |
rs226041379 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825144 | GGTAGCCATGGCAAC[A/T]CCAGAGTCAGAAGGT | 17970 |
rs226083335 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814173 | TAACCACTAAGCCAT[C/T]TCTCCAACCACCATG | 17970 |
rs226113630 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820692 | CCATGAGATCCAGCT[A/G]TAAGGCATTTTCTCA | 17970 |
rs226189528 | in-del | -/AGGAACTGAA | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813912 | CTTGGGGCTAGCTTT[-/AGGAACTGAA]CCCAAGGGTTTTTAG | 17970 |
rs226242972 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812552 | ATAAAACTAAAAAAG[A/G]AAAGAAGAAAGAGAG | 17970 |
rs226300809 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152818078 | GGGGACGCGTGGCCC[A/G]TGGCCCGTCCTGCTC | 17970 |
rs226309716 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152836682 | AAACAGGAAGAGAAA[C/T]CAACCACCCCCCAGA | 17970 |
rs226311528 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152801549 | TCAATTGTTTATTTG[A/G]TTAATTACCCATTCA | 17970 |
rs226314838 | in-del | -/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812907 | TTCTCAGATTTTTTT[-/T]AAGGTTCTTTTTCTT | 17970 |
rs226329846 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798391 | GCAGGAGGTACGGAG[A/G]CAGGAAATGGGTCAG | 17970 |
rs226337145 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152812021 | GTGAGGCTGGGGTGC[-/T]GGGAAGCAGGGGGGA | 17970 |
rs226475906 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152801991 | GAGATGGAGCACGGA[A/G]AGGCAGAGCAGAGGT | 17970 |
rs226530386 | in-del | -/GT | | | intron-variant | Ncf2 | Mm_Celera | 1:152804582 | ACACGTGCATCAGTG[-/GT]TTTTTTTTTTTTCTT | 17970 |
rs226603280 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808609 | TCAACAAGGCAGGGT[A/T]CTTCTTTAAGAATTC | 17970 |
rs226618029 | in-del | -/TTAA | | | intron-variant | Ncf2 | Mm_Celera | 1:152810457 | TTATTATTAATTTTT[-/TTAA]TTAATGTGAGCGGTT | 17970 |
rs226618883 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813265 | AGAAACTTTGAAGGT[C/T]TATGAGCACTAGTGG | 17970 |
rs226659066 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820501 | GACACTGAGGAACCC[A/G]CAATTCAACTCGAGG | 17970 |
rs226670251 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152800973 | AAGATGTGTGGGGCG[G/T]GACACCATTTTATTA | 17970 |
rs226699376 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818786 | AGGTGGTGCGCGCCT[G/T]TAATCTCAGCACTCG | 17970 |
rs226744606 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152823424 | CTGTAGAGGATTAAG[C/T]CAGCCAACCTTCTAG | 17970 |
rs226799222 | in-del | -/GCT | | | intron-variant | Ncf2 | Mm_Celera | 1:152801469 | GGTGGGGTGGGGTAG[-/GCT]GGGAGGATGGATAAC | 17970 |
rs226831942 | in-del | -/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152811673 | GGATAATAATGAAGT[-/C]CCTTTCCCTCCATCA | 17970 |
rs226914110 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819053 | CAGTGTGTTGTACCC[G/T]TGTGCTCACAGACAA | 17970 |
rs226978993 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816930 | GCTTCTTGACGTGGG[C/T]TCTGCATTTCTCTCT | 17970 |
rs227029502 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818011 | AGTGAAGCGTTCCCA[C/T]GGTTGCTTAGAGATG | 17970 |
rs227042702 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152824786 | CTGACTTGAGGTGAG[A/G]CCGTAGGACCTTATC | 17970 |
rs227073302 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799791 | ATGCTTTCAGCTGCT[A/G]CAACAGAGGAATCAA | 17970 |
rs227092559 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152822483 | AAAAAGAGAGTGTTG[A/G]GTAAGTAATACCAAT | 17970 |
rs227183823 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152825960 | AGACTGGCTTTCTCT[-/G]GGAAGTAGACCCCGA | 17970 |
rs227267701 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152800847 | ATGAAAGAAACCACA[-/G]TAACGTTATCTGAAA | 17970 |
rs227284900 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152823817 | TATAAAGATTAAGGA[A/G]GTAAGAGTGGATCTG | 17970 |
rs227382232 | in-del | -/GGGTGAGGTA | | | intron-variant | Ncf2 | Mm_Celera | 1:152801462 | CGGTGGGGTGGGGTG[-/GGGTGAGGTA]GGGTAGGCTGGGAGG | 17970 |
rs227440828 | snp | A/C | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800327 | GTGTTTCTAACTCGT[A/C]ACACTCTTCCTTTTC | 17970 |
rs227447223 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804015 | TTCTTGAGTGAAGGA[C/T]GTTTACTTTTAAGGT | 17970 |
rs227501352 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152800622 | CTGTACCCTGGAGAC[C/T]AGTGAGCCCAAATCA | 17970 |
rs227532524 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820609 | TACCTTGTCCTGGCT[A/G]GTTTTGTGTCAACTT | 17970 |
rs227544820 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152832645 | GAGAGCCACTTAAAT[A/C]TAAGTTAGAGATCCA | 17970 |
rs227563011 | snp | C/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798699 | CACATGCCATTAATC[C/T]CAGAAGTCAGGAGGC | 17970 |
rs227568574 | snp | C/T | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800236 | CTCTCCTCCACCATA[C/T]CTGGGAACAGTCATG | 17970 |
rs227629096 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152823148 | TCCTCATCAGACAAG[-/T]TTTTTTTTTGTGCAG | 17970 |
rs227698085 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152823377 | TAGACATGGCAGGAC[A/C]TCTGCACATAACTCG | 17970 |
rs227705978 | snp | C/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798427 | TTGCTCACCCCTGAT[C/T]GGATCTGATCAAAAC | 17970 |
rs227709295 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802149 | CTGACAATTAACTCC[C/T]GCTAATAGCAGCAGA | 17970 |
rs227740366 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152826159 | CTCATGGGACCTTGC[A/G]CAGCCTCTGCACTCA | 17970 |
rs227745041 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152821202 | TTCTCCCCAACTCTG[G/T]CTCTGCCTCCCCAGG | 17970 |
rs227863835 | in-del | -/TG/TTG | | | intron-variant | Ncf2 | Mm_Celera | 1:152802441 | TGGTGGTTTTTGTTT[-/TG/TTG]TTTTGTTTTGTTTTG | 17970 |
rs227938016 | in-del | -/TT | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813109 | TCACCAGCCCTCAGA[-/TT]TTTTTTTTTAAAAGA | 17970 |
rs228030656 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814984 | GAGGGTTTGTCCCCT[A/C]GACCAGACCACTCAC | 17970 |
rs228103540 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804086 | ACCTGCCTTTCTTGC[G/T]AAAGCTGGATTGAGG | 17970 |
rs228130012 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820635 | AACTTGACACAGGTT[A/G]GAGTTATCACAGAGA | 17970 |
rs228239420 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826060 | CCCTACTCTCAGCCC[C/T]AGTTTACATGGCTGG | 17970 |
rs228251415 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152825648 | CACTTAAAATGGTCA[A/C]TTTGATGATTTGATG | 17970 |
rs228275063 | in-del | -/ATTT | | | intron-variant | Ncf2 | Mm_Celera | 1:152833619 | TTTTTAACTTATTAG[-/ATTT]ATTATTAACTGGTAA | 17970 |
rs228281060 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826767 | AAGGAAAGTCCCAGA[C/T]GACAGACTCTATGGC | 17970 |
rs228292455 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152801915 | TAACATTCAAATTGA[C/T]TGGACCTGGAAAATT | 17970 |
rs228344987 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808351 | AGTTTTAAAAGCTCC[C/T]AGGGCAGGTTTTCAG | 17970 |
rs228384748 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808257 | CCTCTGGAAACCTCA[-/T]CCCCCAGAGCCGGAA | 17970 |
rs228406068 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152812069 | GGAATTGACAGTAAA[A/T]TCCTGGAAGTTTTCA | 17970 |
rs228412862 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152803306 | AGACCTATCAGCAGC[A/G]AGAAGCAATCCTGGT | 17970 |
rs228446589 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152808746 | AGGGTTTCTCTGTAT[A/G]GCCCTGGCTGTCCTG | 17970 |
rs228446856 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802773 | AATAGTCACTATTTT[A/T]TGGTTCTACAAGATC | 17970 |
rs228497719 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152830307 | CCCAGTAAGGGGATA[C/T]GGTCCAAGCTGAATG | 17970 |
rs228517016 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820200 | GGTACCAGCTCACCT[A/G]TCCTCAGAGCTGACT | 17970 |
rs228603209 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152824846 | CATGTGAGTTGCCCA[A/G]TCTGAGTAAGCTAGA | 17970 |
rs228625937 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152800569 | CTTGTGACCAGCTGC[C/T]TCAGGGTCTGACACC | 17970 |
rs228711138 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806272 | TTAAATGTCAGGCTA[G/T]GATGCTGCTGCTGCC | 17970 |
rs228786403 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152800661 | TTCATTACGATGTTT[C/T]TGTCGGAGTGTTTTA | 17970 |
rs228828278 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152801506 | AAGTCTTCAGAAAAA[C/T]GTATGATGAGAATCC | 17970 |
rs228871785 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152818386 | TACAGGTATGAAGGC[C/G]GTGAGCAGGCAGCGC | 17970 |
rs228888384 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806236 | GTAGAAACTGAGAAG[C/G]CAAGGAAATCACTTG | 17970 |
rs228889011 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806661 | TCTTAAGAATCAGTG[C/T]CAAGGATCTGAGACT | 17970 |
rs228900320 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152831098 | GTAAGAGTTGGGGAT[A/G]TAGCTCCAATGGGAG | 17970 |
rs228936501 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152823705 | CAGACAGATCTCTGT[A/G]AACTGCAGGCCAGTC | 17970 |
rs228939242 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798387 | GTGGGCAGGAGGTAC[A/G]GAGACAGGAAATGGG | 17970 |
rs228944204 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152829813 | TTTTTCTTTTTTTTC[C/T]AAGACAGGGTTTCTC | 17970 |
rs228973674 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152810822 | CTGTACCCCGGGGCC[A/G]GTTTTGTCACCTTGA | 17970 |
rs229175879 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152828928 | GGTGATGGGACACTT[A/G]TGACATGAAAGTGGA | 17970 |
rs229211398 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812377 | AATGGGAGCTGGAGA[A/G]ATGCCTTAGAGGATA | 17970 |
rs229214741 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152823686 | AGCACTCCAGAGGCT[A/G]TGACAGACAGATCTC | 17970 |
rs229248060 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825585 | TGGCACCAGATAACA[C/T]GTAGCATTGCAAAGT | 17970 |
rs229261050 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152810183 | CCATAGGCCCTGGAT[A/G]CTTATAACCTGGCCT | 17970 |
rs229268064 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152806594 | AGCATCTTAAAATAG[A/C]CAGGGTGGCAGGCCT | 17970 |
rs229314611 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804312 | AATAAAATAATTGAT[C/T]CTTTCTTTGTGGTTG | 17970 |
rs229368602 | in-del | -/TTGAGGC | | | intron-variant | Ncf2 | Mm_Celera | 1:152827151 | TGGGGAAGGGTTGAG[-/TTGAGGC]TTGAGGTCAATAAAA | 17970 |
rs229369324 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152805655 | TTTGTGTCTTTTATC[G/T]GGGAACTAAATGATC | 17970 |
rs229461030 | in-del | -/AC | | | intron-variant | Ncf2 | Mm_Celera | 1:152831254 | CGTGGCACTCTGATG[-/AC]AGACAGCCTATAGTC | 17970 |
rs229472727 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152828239 | TGCATCCCTCACAAC[A/G]TCAGGCAGGGACTTT | 17970 |
rs229484434 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152827762 | TCACAGTCTCTTTCC[C/T]GTGTGCGTTTTTTCT | 17970 |
rs229508764 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152810669 | GACGTGCAGCAAGCA[A/C]TCTTATCTGCTGAGC | 17970 |
rs229601856 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152823636 | TTTAAAATAAAAAAG[G/T]TTGGATACTGTAGGT | 17970 |
rs229635853 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827031 | GCCATCTCACCAGCT[C/T]GAGAGACTCTTGTCT | 17970 |
rs229640086 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152823070 | TATCACTTGGCTAAA[A/T]GGGCACAGTATCAAC | 17970 |
rs229671186 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152805071 | GCTGTGTGGGTCATG[A/G]CGGCCAGTTGGGGAA | 17970 |
rs229715163 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827384 | TTTTCTCTTGTCATC[C/T]TCCCCTTCTTCATTT | 17970 |
rs229800179 | snp | C/G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822584 | TTTTTTTTTTTTTTG[C/G/T]GGGGGGGGGGGGAGT | 17970 |
rs229819402 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152828381 | GGAGAAGTAACCAGG[A/T]CCTTGAGGGGTCAAT | 17970 |
rs229821339 | in-del | -/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152815788 | TCGTGCAATGGACAT[-/C]GGGGCTGGGGGTGTA | 17970 |
rs229837635 | in-del | -/AAGTAGCACACACACTG | | | intron-variant | Ncf2 | Mm_Celera | 1:152822717 | AGACCACACTGCTTC[-/AAGTAGCACACACACTG]GTCACAGGACATGGA | 17970 |
rs229934464 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152832022 | TACCTAAAGCCGGTG[A/G]GAGGAAAAAGGCTGC | 17970 |
rs229983494 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152827378 | CTCACTTTTTCTCTT[-/G]TCATCTTCCCCTTCT | 17970 |
rs230078386 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804879 | ATGACTGAACCCTCA[C/T]GCTGACTCTGGAGAC | 17970 |
rs230104563 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152832346 | AAGTTGGAGGTGGGG[C/T]ACACTGAGTGCCACA | 17970 |
rs230155329 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799983 | CATACCCTGCCTCCT[A/G]TCCTGAACTCTTGGG | 17970 |
rs230170045 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152830513 | GGGGGTGGGGTGGGG[G/T]GGGGTGGGTGGTTCG | 17970 |
rs230186062 | snp | A/G | | | utr-variant-5-prime, intron-variant | Ncf2 | Mm_Celera | 1:152807689 | GTCCCCCTGACCTGA[A/G]GCTCCCACAGAGGGT | 17970 |
rs230186370 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813791 | AGTTAGGGTGGGTTG[C/T]TTTGTTTTGGTTGGG | 17970 |
rs230264526 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806781 | GGACAATACTCTCTC[C/T]GTAATGTAGAGTGCG | 17970 |
rs230361899 | in-del | -/T/TTTT/TTTTT | | | intron-variant | Ncf2 | Mm_Celera | 1:152822035 | TTGGAAGCAAGAGTG[-/T/TTTT/TTTTT]TTTTTTTTTTTTTGT | 17970 |
rs230423347 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827706 | TGACTACAGTGCACT[C/T]CCCTCCCGCTCAGTG | 17970 |
rs230476516 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152811119 | GGGTAGGAAGGCTGG[C/T]TTGCTTTCTCTAGGC | 17970 |
rs230489044 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816922 | GCAGGAGGGCTTCTT[G/T]ACGTGGGCTCTGCAT | 17970 |
rs230514366 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827349 | CAGTCTGTTCTCTCT[C/T]CCCCCCCCGCCCCCT | 17970 |
rs230530280 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152808451 | TGTGAAGACTTCTTC[A/G]TTTGTGTTTTCTTTT | 17970 |
rs230597036 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152811672 | GGGATAATAATGAAG[C/T]CCCTTTCCCTCCATC | 17970 |
rs230619524 | in-del | -/GCACT | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815179 | GGAGGGAGTGGGGAG[-/GCACT]GTAAGTTATCATTCA | 17970 |
rs230678947 | snp | A/G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152832505 | ACACCACAAAGGAGC[A/G/T]TGGCTTGCCTCCGTG | 17970 |
rs230704167 | in-del | -/AGCTGC | | | intron-variant | Ncf2 | Mm_Celera | 1:152815757 | GGGGGTGAGGAGGGA[-/AGCTGC]AGCCAGGCAAATGAT | 17970 |
rs230732463 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152803566 | GAACAGAAAACAGCT[C/T]TAGAACTGATGGAGT | 17970 |
rs230799124 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152808860 | TTTTCTCTGGCCCGG[A/G]GTTGAACATGCTCGA | 17970 |
rs230945156 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825700 | TTCATATTGTTTGTT[A/T]ATTTAACTAAAAGAG | 17970 |
rs230960688 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802013 | AGCAGAGGTTGATGA[C/T]CTCTGGCCTTTAACC | 17970 |
rs230982110 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152810503 | TGCTTGTTTTGACAA[C/T]ATGTGCGTACCTGAT | 17970 |
rs231008970 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152834714 | CCTCTGATCTGCCGC[C/T]CCCCCCACCCCCATA | 17970 |
rs231011086 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152831283 | GTCTCTCTTCACACT[C/G]AAGAACAGCGTGTGC | 17970 |
rs231129640 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815563 | CTGTTTCTCGGCAGA[C/T]GTCTTAGGAAGCCTC | 17970 |
rs231180230 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806734 | AGGTTGAGAGGAAAT[G/T]CGGTCATTATTTCGG | 17970 |
rs231234198 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152831812 | CTTGCTTTACCTAGC[A/G]TGCTCCTTGTTTTAC | 17970 |
rs231248852 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809967 | GAAAAAACACATCCA[C/G]ATCCTGACAGGAGGA | 17970 |
rs231251110 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816037 | AGCTGCCCCATCCAC[C/T]AGCTCCTTCTTACAA | 17970 |
rs231325708 | snp | A/C | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798625 | ATACCCAGGGCTACA[A/C]AGAAAAACCCTGTCC | 17970 |
rs231329264 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152803786 | TTGGCACTTAGAATA[A/G]CAGTGATTGATCTTT | 17970 |
rs231400514 | in-del | -/GCT | | | intron-variant | Ncf2 | Mm_Celera | 1:152820293 | CCAGCACCAGCACCA[-/GCT]ATTACCTCCATGGAA | 17970 |
rs231470797 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152812131 | ACTATGAACAAAGAA[A/G]ACTGGTGCTTGGGAA | 17970 |
rs231517546 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152829833 | CAGGGTTTCTCTGTG[C/T]AGCCCTGGCTGTCCT | 17970 |
rs231616800 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152806582 | TCTTTTGGTCTTAGC[A/C]TCTTAAAATAGCCAG | 17970 |
rs231626949 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152833192 | CTGGAAGCAGACACC[A/G]GCTCTGCTCACACAT | 17970 |
rs231701696 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809100 | GCTACGTATGTCATG[A/G]CGCACATGTGTCAAT | 17970 |
rs231862823 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152828900 | AAGGAAGGTTAGAGA[A/G]AGGGAGGGACAGGGT | 17970 |
rs231878577 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822120 | GGGCACATGTGGGTA[G/T]GTGGCCGTAGCATCC | 17970 |
rs231961726 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152828232 | AAGAGGCTGCATCCC[C/T]CACAACGTCAGGCAG | 17970 |
rs232025077 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813118 | CCTCAGATTTTTTTT[A/T]AAAAGATTTATTTAT | 17970 |
rs232053041 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152830196 | TCGCCTTGTCTTCTC[A/G]GGGTCCTGGGTGGCA | 17970 |
rs232113177 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813948 | TTAGCAGGGGGAGAA[A/G]GGTAAAAGCCAAAGC | 17970 |
rs232115217 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820483 | CAGCATTATAATAAA[A/G]CAGACACTGAGGAAC | 17970 |
rs232217483 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152809631 | AACTGAAGCTCCTTT[C/T]TCTGTGATAACTCCA | 17970 |
rs232240897 | in-del | -/TGGTT | | | intron-variant | Ncf2 | Mm_Celera | 1:152804580 | GCACACGTGCATCAG[-/TGGTT]TGTTTTTTTTTTTTC | 17970 |
rs232255584 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152818702 | GCTTCTCAACTTATG[A/G]TGACAAGTTCTGTCC | 17970 |
rs232272886 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815470 | CAGAGGTTACCAAGG[A/G]GTCCCTATGGGGTTG | 17970 |
rs232311586 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814460 | TACCGCTCCAGCCCT[C/T]AAGGCAACATTTAAT | 17970 |
rs232389222 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152800890 | ACTGCGATGGGATAG[C/T]GTGTGGGGGTTCAGC | 17970 |
rs232443608 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816011 | TTAACAAATGGGCAA[G/T]ACGTTAGCAGAGCTG | 17970 |
rs232444444 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152824428 | GAAGACACGCCCCCT[C/T]TCCCTGCCCTGTGGC | 17970 |
rs232463246 | in-del | -/CTGTTGGAATTT | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815335 | ATTGGCCCTGACCAC[-/CTGTTGGAATTT]CAGGGGCAGCATGCT | 17970 |
rs232469872 | in-del | -/TT | | | intron-variant | Ncf2 | Mm_Celera | 1:152832809 | CAGTGTCCCTCATAG[-/TT]TTTTTTTTCTTACCT | 17970 |
rs232558834 | in-del | -/TT | | | intron-variant | Ncf2 | Mm_Celera | 1:152829793 | GGAGGCTCACATTTC[-/TT]TTTTTTTTCTTTTTT | 17970 |
rs232616553 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152810293 | ACCAGGCCTCTCATC[C/T]CATCTGTCATAGTCT | 17970 |
rs232645699 | in-del | -/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152821900 | CGGTGAAGACAGAGG[-/C]TGTTTGCTTGCCTGA | 17970 |
rs232746001 | snp | C/T | | | missense | Ncf2 | Mm_Celera | 1:152833781 | TCCTGCCTCAGGAAC[C/T]GAAGCTCAGCGTGCC | 17970 |
rs232849978 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822647 | GGGAAGTATCCCACA[C/T]TTGGCACTGAGCTTC | 17970 |
rs232861684 | in-del | -/AA | | | intron-variant | Ncf2 | Mm_Celera | 1:152810136 | GAGAGCTGTGGAGAC[-/AA]ACGGAGGCAGCTCTC | 17970 |
rs232952707 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809257 | CTTCACCTGCTTCTT[C/G]TTGTTGTTGTTGTTT | 17970 |
rs232995245 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152818485 | GGTCAAAATGACCCA[A/G]GGGTCAAGAAACTAG | 17970 |
rs233042115 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152832518 | GCATGGCTTGCCTCC[-/G]TGCATGTCAGGGCGT | 17970 |
rs233064162 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152836989 | TAAATCCTCTACACA[C/T]CGATCTGCTTGGAGA | 17970 |
rs233119024 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813082 | AGTCAGTGCTCTTAC[C/T]GGCTGAGCCATCTCA | 17970 |
rs233262099 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152820788 | CTATAAGAAAGCAGG[C/T]TGAGCAAGCCAGGGG | 17970 |
rs233285646 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152818952 | aacaaaacaaaaaaa[A/C]aaaaaaaaGGAgaaa | 17970 |
rs233294518 | in-del | -/CTGGGAAGGGGAGGCAAG | | | intron-variant | Ncf2 | Mm_Celera | 1:152811168 | AAGCAAGAGGCTTTT[-/CTGGGAAGGGGAGGCAAG]CCTGACCTCATTGTA | 17970 |
rs233351594 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814903 | AGAGGTGAGTTGATA[C/T]TGAATGGGTTAGGCA | 17970 |
rs233392184 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152811453 | CCCTGTCACAAAAAT[A/T]AGAATACAAACTGTT | 17970 |
rs233422359 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798230 | AAAAAAAAAAAAAGT[A/G]CCTCGGGCCTGTAAA | 17970 |
rs233477500 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152803761 | TCCAGTTCCGCGCTG[A/G]ACAGTATCATTGGCA | 17970 |
rs233509911 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827072 | TGCTGAGTTGATTTT[A/T]AATATCCAGAAATGT | 17970 |
rs233585591 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798538 | TGACTCAAAATTGTG[A/G]TAGTGGTCCTATTTT | 17970 |
rs233684779 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813249 | CTGACCACGTCTAAG[A/G]AGAAACTTTGAAGGT | 17970 |
rs233703292 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813598 | AGAGACAAAGGGCAG[A/G]GAATAAAAGACAAAG | 17970 |
rs233714082 | snp | A/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152800060 | TGCTGTCTTTGTGCC[A/T]TTGGGCCTCCTGGCT | 17970 |
rs233723817 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816133 | TGATGAGACAGAGAA[C/T]TGCACGGAGAACTTT | 17970 |
rs233724789 | snp | A/G | | | missense | Ncf2 | Mm_Celera | 1:152835079 | AAAACTCAGACGCCA[A/G]TAAGCAGACTACGGA | 17970 |
rs233729682 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815292 | AGAAAGGGGAGGAGG[C/T]AAAGCCTTCTTCCTG | 17970 |
rs233811959 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152822761 | GGAGAAATCATGTTG[A/C]TACTGAGCAAGAAGC | 17970 |
rs233815203 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814670 | CCTCTAACAAGCCCA[C/T]ACCTTCTAATAGTCA | 17970 |
rs233917063 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152832573 | AAATGGAAACAACCC[A/G]TCAGCTACTTACATT | 17970 |
rs233951855 | snp | C/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799729 | AGGAGGGAGCATGGA[C/T]GCTTCACTTACTGTC | 17970 |
rs234030605 | snp | C/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799490 | TGTCCTAGAACACTC[C/T]GTAGACCAGGCTGGT | 17970 |
rs234088587 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819084 | GCAGTAGGGAAACCC[G/T]GGATGTTAAACACAG | 17970 |
rs234204460 | in-del | -/CTC | | | intron-variant | Ncf2 | Mm_Celera | 1:152811275 | TGGCTACCCAGCCCT[-/CTC]AACAATGTCCTTAAT | 17970 |
rs234218486 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152817137 | GCGAGGGAAGCACAA[A/C]GGTCTAGCTGTTGTG | 17970 |
rs234259646 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152822418 | GTGCCCTCTATGCTG[A/G]GACAGAAATTCAAGA | 17970 |
rs234308807 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819221 | ACCACACTTGGTTTC[C/T]CACCATAAGCTTGTT | 17970 |
rs234365594 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152812052 | TACCCTGAAGGGGGA[G/T]GGGAATTGACAGTAA | 17970 |
rs234372806 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152824153 | CATGAGCTCACCTAA[C/T]AACGTCTGGCTCAGA | 17970 |
rs234377367 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152801031 | CAGAATGTTAGGTGC[A/T]AGGTTCTGTGGGAAA | 17970 |
rs234392427 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804933 | TCTGTCATAAGGACG[C/T]TTGGAAAGGAAGAGT | 17970 |
rs234416391 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152817821 | AAAGGACAGGCATGG[A/C]TGGCTTTGACTTGTG | 17970 |
rs234453862 | in-del | -/AAAAA | | | intron-variant | Ncf2 | Mm_Celera | 1:152827849 | GGCCTAATCTCAGCT[-/AAAAA]AAAAAAATCCTTCTA | 17970 |
rs234474101 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152829953 | TGTCACCACCACCCA[G/T]CGGAGGCTCACATTT | 17970 |
rs234499167 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152824916 | TGAGACATCAATTCA[C/T]GAATGGATATATGCA | 17970 |
rs234635086 | snp | A/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798169 | TACAGAGTGAGTTCC[A/T]GGACAGCCAGGGCTA | 17970 |
rs234667344 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152805984 | GGTTTGAGGTCTGTC[A/C]TGGGGTAAAGACACA | 17970 |
rs234696655 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152803622 | TGTGCCTCAGTGAGG[C/T]GGAACCCTGAGGAGT | 17970 |
rs234699677 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152829396 | AAATAAAGTAAAAAT[A/G]TTATCTTTTGGGAAG | 17970 |
rs234710463 | in-del | -/A | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152807986 | CCCGGCAGCTCTGAG[-/A]GAGACACCTTGAACT | 17970 |
rs234745062 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819420 | AGAAATTCACTGCCC[C/T]TGCCTCCCAAGTGCT | 17970 |
rs234799645 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152800779 | TCCTCGGTGCGAGAG[C/T]CCTTGCCTGAGGAAG | 17970 |
rs234821311 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812732 | GAAAGGATCACAAAT[A/G]GGCTTCCAAATGCAA | 17970 |
rs234848628 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152810576 | AATTTCAGATGGTTG[G/T]GAGCCACTATGTGGG | 17970 |
rs234878307 | in-del | -/CT | | | intron-variant | Ncf2 | Mm_Celera | 1:152831711 | GCCCCGAGGAAGGAG[-/CT]CTCTCTCTCTCAGAT | 17970 |
rs234922596 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152835821 | ATTCTACATTTTACT[A/G]TGTATTTATTGCATC | 17970 |
rs234933460 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825202 | GACTACCCATAGTAG[C/T]CAGCTCGGAGTTTGA | 17970 |
rs234993020 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152811057 | CGCCTGATGGATCGG[C/G]CTTTCTTCTGTAGTC | 17970 |
rs234993307 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152805339 | CCCCAAGTCATTCCC[A/G]ATTGGTTAATAAAGA | 17970 |
rs235051820 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152826222 | AGGCGTGTGAGTTGC[A/C]GGGGATAGGGTGCCA | 17970 |
rs235127415 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152800963 | AAAGAGAGCTAAGAT[A/G]TGTGGGGCGTGACAC | 17970 |
rs235135496 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799720 | CCAGAAAAGAGGAGG[A/G]AGCATGGATGCTTCA | 17970 |
rs235185839 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152806334 | AGGAGGAAGATCACA[A/C]CATTGCTTATAAAAA | 17970 |
rs235208039 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152808744 | ACAGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTCC | 17970 |
rs235244235 | in-del | -/TTGTT | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813788 | CTGAGTTAGGGTGGG[-/TTGTT]TTGTTTTGGTTGGGC | 17970 |
rs235275461 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152801772 | GCTACCTGTGGCTAT[C/T]TAAAGTCACGTAGAA | 17970 |
rs235277867 | snp | C/T | | | utr-variant-5-prime, intron-variant | Ncf2 | Mm_Celera | 1:152807438 | CTGAAGATTCTCCAT[C/T]CTGTCTCAGAAATAT | 17970 |
rs235332227 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152801348 | AGTGAGATCCTGTCT[C/T]AAAATCATTTTTTAA | 17970 |
rs235367678 | snp | C/T | | | synonymous-codon | Ncf2 | Mm_Celera | 1:152821605 | AACCAACATGAAGTC[C/T]GAGCCCAGGCATTCC | 17970 |
rs235388624 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825622 | GGTATATGAAATACC[A/T]CAGAAATGTTCACTT | 17970 |
rs235497078 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152829238 | CGACTCACTGCGCTG[C/G]AGCCTCAAACTCACA | 17970 |
rs235536930 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806785 | AATACTCTCTCCGTA[A/T]TGTAGAGTGCGGAGT | 17970 |
rs235565538 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152823417 | TGGTTGCCTGTAGAG[A/G]ATTAAGTCAGCCAAC | 17970 |
rs235633576 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152805214 | GTGGACCTGCCTATT[C/G]AGGATTGGTCTGTTA | 17970 |
rs235651107 | in-del | -/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152817255 | GTGAAAAAGTGTTTT[-/C]CCCGGCATGGCATGC | 17970 |
rs235685751 | in-del | -/TATTTATT | | | intron-variant | Ncf2 | Mm_Celera | 1:152826833 | ACTCTTTTTTCAAAA[-/TATTTATT]TATTTATTTATTTAT | 17970 |
rs235778053 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152830994 | GGCAGCAAAGCCTAA[C/T]GGTTTAGGGCTAGGT | 17970 |
rs235778389 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815531 | GAGCCAAGAGCCTGC[C/T]TGCTCTGGGGGTGTG | 17970 |
rs235946655 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152807084 | TCATCAACTATATTT[C/T]GCCTACCAAGAAGTC | 17970 |
rs235952848 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152820512 | ACCCACAATTCAACT[C/T]GAGGCCTGGGATGTT | 17970 |
rs235957136 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806653 | CAATCATTTCTTAAG[A/G]ATCAGTGTCAAGGAT | 17970 |
rs235958933 | snp | A/G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812442 | CAGTTCCCAGCAACC[A/G/T]CGTGGTGGCTCACAA | 17970 |
rs236022554 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152828205 | GAGCTCATTCCCCAA[-/T]TCTCTAAACTAAAGA | 17970 |
rs236033424 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802859 | AGACAAATCATCTGC[C/T]TTGTGTCTTATTATT | 17970 |
rs236163907 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827885 | GCGTGGTGGTGCACG[C/T]CTTTAATCCCAGCAC | 17970 |
rs236228851 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152811996 | CCCATCAATGAAACT[A/G]GACAAGTGTGGTGAG | 17970 |
rs236238212 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152828443 | AAGTGCTGCAGTTTC[C/T]CTACTGTGCCTTCCA | 17970 |
rs236240528 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152830119 | GTTCTTGGATCCCAT[C/G]GTGGTGTTCCCTGGG | 17970 |
rs236257029 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819338 | TTGTTTTGTGACAGA[-/T]TTTTTTTTTCTGTGT | 17970 |
rs236272733 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809339 | ATGACCAAGAAGCAA[A/G]CTGGGGAGGAAAGGG | 17970 |
rs236302469 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152828099 | GGAACAAAGCAAGCC[A/G]TCTTCCTCCTCCAAT | 17970 |
rs236303658 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152834535 | GCTGTCTTAGTAGGT[A/T]TGAGATAGATCTTCA | 17970 |
rs236352759 | in-del | -/CT | | | intron-variant | Ncf2 | Mm_Celera | 1:152803501 | TAGCATAAAAACAAA[-/CT]CAGCATTTATGCCTG | 17970 |
rs236353519 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818736 | TATGAGCCACATCCT[C/T]AGTGGCTCCTCAATA | 17970 |
rs236419515 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152804899 | ACTCTGGAGACAAGA[A/G]CTTGAACAGAACTTG | 17970 |
rs236475220 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152827009 | AGTCGGCACTCTTAA[A/C]GGCTGAGCCATCTCA | 17970 |
rs236522189 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152833979 | AGGGGTGGATGATGG[A/G]GTGGGTCTTGTCTGA | 17970 |
rs236551650 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152809181 | TGACCGACCCCAAAT[A/C]TCTGAGATTGCACAG | 17970 |
rs236675850 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825769 | TCCCTCCAAAAGCTA[C/T]CTGAGTGACAATGGC | 17970 |
rs236804241 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809362 | GGAAAGGGTTTATTC[A/G]GCTTACACTTCCATC | 17970 |
rs236830035 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152832957 | TCCTCAGTAGTAAAG[C/G]GTCTCAGACTTCACT | 17970 |
rs236845747 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813568 | CTCAACACAAAGGAG[G/T]TTTATTTGCCCCAGA | 17970 |
rs236933714 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152808269 | TCATCCCCCAGAGCC[A/G]GAAAGGAACAAAAGC | 17970 |
rs236939208 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814094 | GGGGCTATGGATGGA[G/T]ATGAGCCACCATGTG | 17970 |
rs236991777 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152834643 | ATTTGCTGTCTGGCC[C/T]GATGACTTGAGCCCG | 17970 |
rs237001298 | in-del | -/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798549 | GTGGTAGTGGTCCTA[-/T]TTTTTTCCCTCGGGA | 17970 |
rs237094650 | in-del | -/A | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152807992 | AGCTCTGAGAGAGAC[-/A]CCTTGAACTACCATC | 17970 |
rs237126545 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152824061 | GAGAGATACAAAGAT[A/G]TTTTAGCCAACCAAT | 17970 |
rs237140197 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812361 | CGCCTTAAGGATAAC[A/T]AATGGGAGCTGGAGA | 17970 |
rs237176953 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152809482 | ACTGGCTTGCTTCCA[C/T]TGGCTTGCTCAGCCT | 17970 |
rs237192079 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815360 | CATGCTGGGGGTGCG[A/G]CCTGTTTCGACTCCT | 17970 |
rs237201333 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806341 | AGATCACAACATTGC[C/T]TATAAAAAGCCTTGT | 17970 |
rs237264103 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152830015 | AGGATTGCTGGAAGT[A/C]CAGGCCAGCAAGTGC | 17970 |
rs237271469 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152828877 | AGGATCGGCTGTCAG[A/G]CCAGGAGAAGGAAGG | 17970 |
rs237341557 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152836527 | ATGTAATCCTGAAGG[C/T]ACACACAGACAACTC | 17970 |
rs237478622 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152820049 | TGTGGCTAAAGGCCG[A/T]TGACCTTAGTTAAAA | 17970 |
rs237484583 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804961 | AGTGGCAGAAAGGTC[G/T]TCGGCTAGCAGTGGG | 17970 |
rs237501193 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152802276 | AAAagagagagagag[A/G]gagagagagagagag | 17970 |
rs237502928 | in-del | -/TT | | | intron-variant | Ncf2 | Mm_Celera | 1:152825691 | CAGCAGTTTTTCATA[-/TT]GTTTGTTTATTTAAC | 17970 |
rs237518792 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814707 | CTATTTGTATGGTCT[A/T]TGGGGGCCAATTCCA | 17970 |
rs237527160 | snp | A/G | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800359 | TGTGATGACAAGGTC[A/G]GTGTGAAGCTTTGTG | 17970 |
rs237542134 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806040 | AGAATGACTGTCTTA[C/T]GGGAGGTGACTGCTG | 17970 |
rs237558879 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152811085 | GTCTTGGTATTCAAT[C/T]AGGACCTCCAGCTTT | 17970 |
rs237753908 | in-del | -/CCCATTA | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814375 | AAGAGGGCATCAGAT[-/CCCATTA]CAGATGGTTGTGAGC | 17970 |
rs237771034 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152835758 | AGCTCAGATAAAACT[A/G]CTTCTTAAAAACAAT | 17970 |
rs237813944 | in-del | -/CTTTCTTT | | | intron-variant | Ncf2 | Mm_Celera | 1:152819275 | ATCTTTCCTTCCTTC[-/CTTTCTTT]CTTTCTTTCTTTCTT | 17970 |
rs237884719 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152827529 | GACGGCAGTAAGGAT[C/G]TAAAGGATGGTAGGC | 17970 |
rs237952052 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152810723 | TTTTACAGAGGAAAA[C/T]AAGGAGGTTCAAGAA | 17970 |
rs237998089 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152821010 | ACACCTCCCTTAGAC[G/T]TTGACCACGGAGTTG | 17970 |
rs238030619 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152835001 | CTGGCTATGAATGAG[C/T]AAAAACAGGCCCTTT | 17970 |
rs238048482 | in-del | -/TGTGTC | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799666 | GTGTTTCGGTCCAAA[-/TGTGTC]TGTGGGCCGTGCTTT | 17970 |
rs238069283 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152834586 | GGGTGAATTCAATGC[C/T]GAGCTTAGTTAAGGA | 17970 |
rs238111466 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152803834 | GAACATATTAATGAT[G/T]CAACCCCCAGCCTCA | 17970 |
rs238161887 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815556 | GGTGTGGCTGTTTCT[A/C]GGCAGATGTCTTAGG | 17970 |
rs238190112 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152809028 | ATGACCAGCAGGCCT[C/T]TTGATTGCTTAGGTG | 17970 |
rs238323258 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152819657 | GTTTGCACCAACACC[A/G]GCTACTTAGTCGTGC | 17970 |
rs238359643 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818229 | AAACGCTTTGTTACA[G/T]GGCCTGCCCTGTGCC | 17970 |
rs238376734 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152803060 | GAGCAATAAGCTCAT[-/A]GAACCTGAAGGTTTA | 17970 |
rs238453435 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152817586 | GCATATTTTACTCAT[A/C]AATTTGCATATGACA | 17970 |
rs238610998 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152833031 | TAAACACACACAAAA[C/T]AGGGCCATGAAATGG | 17970 |
rs238641361 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152823495 | GAGCTATGGACAGTT[C/G]GTGGCTTCTAGGGGA | 17970 |
rs238661344 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152829033 | TAAGTAAGTAAAAGG[-/T]CCCAGGGCAGGGGGA | 17970 |
rs238708203 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152823007 | CTGCAGAACTGAGCA[C/T]GGACCCATCACTGGG | 17970 |
rs238745250 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814225 | CCTTGAGATCTGAGC[A/T]CAGGTCTCATGCTTG | 17970 |
rs238773663 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152804378 | GAAAATTACCTTGCC[C/G]GCTTACACTTTGTTA | 17970 |
rs238788577 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152826260 | GAGCCTGGGGGCTTT[A/G]ACTTCCTTGGTGCTG | 17970 |
rs238858775 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799945 | TCCTCCACCCTCTAC[A/G]TGTCACAGAGCCTCC | 17970 |
rs238867449 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808981 | ATCCGCCTGCCTCTG[C/T]TTCCCAAGTGCTGGG | 17970 |
rs238906960 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152823080 | CTAAAAGGGCACAGT[A/G]TCAACTGCCCTCTAA | 17970 |
rs238911425 | in-del | -/TT | | | intron-variant | Ncf2 | Mm_Celera | 1:152819337 | TTGTTTTGTGACAGA[-/TT]TTTTTTTTTTCTGTG | 17970 |
rs239032611 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152837580 | AAAAAAAGAAAAAAG[-/A]AAAAAAAATCCAAAT | 17970 |
rs239061228 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820259 | GGGTTGATCCTGGCT[A/G]ccagcgccagcgcca | 17970 |
rs239113951 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825043 | GATGCCATGGCCAAG[G/T]GCTGAAGATAGCTCA | 17970 |
rs239128668 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152821961 | CAATGTGGTTCCCAC[-/A]AAAAATGTTCCAGTT | 17970 |
rs239187691 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813508 | TTAAGATTATTTTAC[A/G]TATGGAAGGACCAGA | 17970 |
rs239188822 | snp | A/G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152802915 | CATCACTTATTTTCT[A/G/T]TCCTTGCACCTACAA | 17970 |
rs239224890 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152801828 | TTTTCCTTCCTTCTC[C/T]TCTGTCTCTGTCTCC | 17970 |
rs239284828 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152819455 | TAAAGGCATGCACTA[C/G]CACCCAGCTCGCTCA | 17970 |
rs239362118 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152815865 | CACTTGATTCCCCCA[G/T]CATACACTGGGTACA | 17970 |
rs239365936 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152811732 | TCGTAAGTAAAAAGA[A/T]AAACCAAATCAAACA | 17970 |
rs239369117 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818353 | TGTCACTCACCCTGC[C/T]GAGGGCCGCTTGTCA | 17970 |
rs239373500 | snp | G/T | | | synonymous-codon | Ncf2 | Mm_Celera | 1:152830364 | CAGGGCTCTGGAAGG[G/T]GAGGCACACCGCGTA | 17970 |
rs239402294 | snp | A/G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152818771 | GAAAGTTGCCAGGCA[A/G/T]GGTGGTGCGCGCCTT | 17970 |
rs239452329 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812806 | GGATCTCTCAGCAAT[A/T]GAGTTAGGGTTGAGA | 17970 |
rs239458075 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152819009 | ACACACCTACCCCAC[C/G]TGCATCATTGCTTTC | 17970 |
rs239553203 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152803410 | TTGTTTGCCCTGGTC[-/T]TTCCTAGATGACTTC | 17970 |
rs239579403 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152801798 | TAGAATCTAGATCAT[C/T]TTTCTCTTGCTCCAT | 17970 |
rs239623268 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152811802 | AAAGAACACACACAC[-/A]AACACATACACACAC | 17970 |
rs239634828 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152817366 | AGGGGAGGGAGATTT[C/G]ATGATTTCGCACTCC | 17970 |
rs239735597 | snp | A/G | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800379 | GAAGCTTTGTGTTTC[A/G]AGCTTGACAGGATCT | 17970 |
rs239857492 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815487 | TCCCTATGGGGTTGG[C/T]GACAGAAACGCCAAG | 17970 |
rs239927612 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826083 | ATGGCTGGTTGGGAG[C/T]CGGCCCTGTCAGCTC | 17970 |
rs240014256 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152826435 | ATTAAGGAGACCTCA[A/G]GCTTGGTTGCATAAC | 17970 |
rs240093010 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802592 | TGCTGGGATTAAAGG[C/T]GTGCGCCACCACGCC | 17970 |
rs240099985 | in-del | -/AAAACAAAAC | | | intron-variant | Ncf2 | Mm_Celera | 1:152816084 | ACTTGTCCTTTTTCT[-/AAAACAAAAC]AAAACAAAACAAAAC | 17970 |
rs240110909 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152801960 | TGCTGGGGTCCCACC[C/T]CCACATTCAGGTACT | 17970 |
rs240130229 | in-del | -/TTCCTG | | | intron-variant | Ncf2 | Mm_Celera | 1:152806957 | CTCCTCCTCTTCTTC[-/TTCCTG]CTCCTCCTCCTCTTT | 17970 |
rs240254742 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822686 | GCATCATGCTCTGTG[C/T]AGGGTAGCTCCAACA | 17970 |
rs240323495 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152809411 | GAAGTCAGGACTGGA[A/C]CTCAAGCAGGTCAGG | 17970 |
rs240378173 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152807243 | GTAAAGAAATCCTAA[A/G]TCTGTGTTTACAGAG | 17970 |
rs240434489 | snp | C/G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152810075 | GCCTGGAGGGAGGAA[C/G/T]GCCTCCTCCTACTTC | 17970 |
rs240493751 | in-del | -/GGG | | | intron-variant | Ncf2 | Mm_Celera | 1:152835578 | TTCTTGTGAAAATCT[-/GGG]TGTGGCCACCATTCA | 17970 |
rs240543335 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799339 | GGAAAAACTGAGCTC[A/G]GGTGCTTCTCAGTCT | 17970 |
rs240595164 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815110 | CTCCCATCAAACTTC[C/T]CTGTCCCGACCTTGT | 17970 |
rs240609548 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152820751 | GTGGGTGGGACCATC[C/T]CTGGGCTGGTAGTCT | 17970 |
rs240706068 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152821354 | CTTAACACCGCTTAT[A/G]TCTGATATAACTCAG | 17970 |
rs240779920 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798378 | AGATGACATGTGGGC[A/G]GGAGGTACGGAGACA | 17970 |
rs240781420 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152804659 | GGCTGTCCTGGAACT[C/G]ACTCTGTAGACCAGG | 17970 |
rs240792318 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819771 | CCACACCAACCTTCT[C/T]GCCTCCTACAGAGAG | 17970 |
rs240793604 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152803961 | TTAGTGATTCTGATG[G/T]AGAGAATCTTGGGGA | 17970 |
rs240821119 | in-del | -/GG | | | intron-variant | Ncf2 | Mm_Celera | 1:152822563 | AAAATAGTCTGTATT[-/GG]GTTTTTTTTTTTTTT | 17970 |
rs240884093 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813585 | TTATTTGCCCCAGAG[A/G]GACAAAGGGCAGGGA | 17970 |
rs240948060 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814212 | TTGTTACGTGAGTCC[C/T]TGAGATCTGAGCACA | 17970 |
rs240948182 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152823425 | TGTAGAGGATTAAGT[C/T]AGCCAACCTTCTAGG | 17970 |
rs241031386 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152832617 | TTGGACTCTTCTCTA[C/T]CCCTCCTCCCCTGAG | 17970 |
rs241094703 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152816014 | ACAAATGGGCAATAC[A/G]TTAGCAGAGCTGCCC | 17970 |
rs241128430 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822926 | GTGGCATGCGTGCTC[C/T]GGGGTAACCAACTGC | 17970 |
rs241169049 | snp | C/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813914 | TGGGGCTAGCTTTAG[C/G]AACTGAACCCAAGGG | 17970 |
rs241244701 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152805013 | TCCCTGCTCTGAGAA[A/C]ATCATTACGAGCTGA | 17970 |
rs241257611 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152810031 | GTCAGCAAGCAGATG[A/G]TGCAGAGCACGGCCC | 17970 |
rs241262853 | in-del | -/TG | | | intron-variant | Ncf2 | Mm_Celera | 1:152819188 | TCGCCTGGTGACCTT[-/TG]TGTGCTTTGTGCCCA | 17970 |
rs241284507 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152801368 | TCATTTTTTAAAAGC[C/T]GGGGAAGGGGCTGGA | 17970 |
rs241291428 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152829451 | TTCAAGTACCCTCTG[-/T]GTTCATTAACAATGG | 17970 |
rs241326217 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152810700 | CATCTCTCTGTCCCC[A/T]TCACTTATTTTACAG | 17970 |
rs241336190 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809846 | AAACTTGGACTCTGT[A/G]GGCTGTGAGGCTTGT | 17970 |
rs241374780 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827683 | GAGGTGAGAGGTCAG[-/T]TTTGTACTGACTACA | 17970 |
rs241494010 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826543 | CATCTGCATATATAC[A/T]GTCTCTGGGGTAGCA | 17970 |
rs241503094 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152809559 | ACAAGGGCCTTTCCC[A/C]CTTGATCACTAACTG | 17970 |
rs241543735 | in-del | -/CA | | | intron-variant | Ncf2 | Mm_Celera | 1:152800701 | GAAAATTGACTACTT[-/CA]CAGCTTCTCCTCCTG | 17970 |
rs241732017 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152830182 | CTCACATGGTGTTCT[C/T]GCCTTGTCTTCTCGG | 17970 |
rs241745787 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798525 | TTTGCTTTAAATTTG[A/G]CTCAAAATTGTGGTA | 17970 |
rs241754996 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152825209 | CATAGTAGTCAGCTC[A/G]GAGTTTGATTGAGAG | 17970 |
rs241765332 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152831518 | TTTCCTGTGTCATAG[A/C]GTTCCACTTTAGGAA | 17970 |
rs241803939 | snp | C/G | | | synonymous-codon | Ncf2 | Mm_Celera | 1:152830704 | GCAGAAGGGGCTTGT[C/G]CCCTGCAACTACCTG | 17970 |
rs241873587 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806487 | GCATGCTGGATAAGA[C/G]CTCTAGCTCTGAACT | 17970 |
rs241883547 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806120 | GGCCAACTGGGAGAA[A/G]CTAGATGAGCTAGCT | 17970 |
rs241908266 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152830251 | GTAAGATGTGGAATT[-/A]AGAGTGAGTGCCAAG | 17970 |
rs241919557 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812319 | TGGATACTTACAGAC[C/T]GAGCTGAGTGCTTTG | 17970 |
rs241933782 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818123 | AGCTACGCCATTGCT[C/T]ACAAGGGAAGACTTG | 17970 |
rs241999697 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152801217 | CAAAACTGATTCTCT[A/G]AGGACAGGCAGGTGG | 17970 |
rs242045874 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152805509 | GAAGGCTGGCCAATC[A/G]GAGTGAGAGCAGTGC | 17970 |
rs242094618 | in-del | -/A | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798210 | CTTATCTCGAAAACC[-/A]AAAAAAAAAAAAAAA | 17970 |
rs242165391 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152804952 | GAAAGGAAGAGTGGC[A/G]GAAAGGTCGTCGGCT | 17970 |
rs242199987 | snp | G/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152800007 | TCTTGGGCCTTGAGG[G/T]CTGCTCTTCCCTACA | 17970 |
rs242324146 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822347 | GTATGCCTGTGTACA[C/T]GAATAATACTTGTTC | 17970 |
rs242350683 | snp | A/G | | | utr-variant-3-prime | Ncf2 | Mm_Celera | 1:152836251 | TTGAACCTGTCACAC[A/G]GCAATATGACAACTC | 17970 |
rs242368230 | snp | C/G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152801922 | CAAATTGATTGGACC[C/G/T]GGAAAATTCTGCTAC | 17970 |
rs242445309 | in-del | -/TTC | | | intron-variant | Ncf2 | Mm_Celera | 1:152802037 | TTTAACCCTCTCTTG[-/TTC]TTCTGGGCCAACAGC | 17970 |
rs242483653 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152829917 | TGCTTTTGCCTCCCG[A/C]GTGCTGGGATTAAAG | 17970 |
rs242503518 | in-del | -/TC | | | intron-variant | Ncf2 | Mm_Celera | 1:152800660 | CTTCATTACGATGTT[-/TC]TGTCGGAGTGTTTTA | 17970 |
rs242527776 | in-del | -/GAGTGAGGCTC | | | intron-variant | Ncf2 | Mm_Celera | 1:152827153 | GGGAAGGGTTGAGTT[-/GAGTGAGGCTC]GAGGTCAATAAAACC | 17970 |
rs242566957 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152828216 | CCAATTCTCTAAACT[A/G]AAGAGGCTGCATCCC | 17970 |
rs242570027 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813441 | ggatctgtctctgca[G/T]ccccagatctgggat | 17970 |
rs242874008 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816040 | TGCCCCATCCACCAG[C/T]TCCTTCTTACAAAAC | 17970 |
rs242879939 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152822023 | AGTTTGATTCCATTT[A/G]GAAGCAAGAGTGTTT | 17970 |
rs242892600 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152827624 | GGTGCCCCAGTGGGC[A/G]TGGTCACCTTACAAT | 17970 |
rs242897130 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804744 | AGGCATGCGACACCA[C/T]GCTCGGCTGTACATC | 17970 |
rs242950532 | snp | C/G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827243 | TGGGCGGCAGGCTTT[C/G/T]GGTTTCCCAAATTGT | 17970 |
rs242956766 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152820594 | TGCTGACTCTCTTTC[C/T]ACCTTGTCCTGGCTG | 17970 |
rs242993692 | in-del | -/GG | | | intron-variant | Ncf2 | Mm_Celera | 1:152812030 | GGGGTGCGGGAAGCA[-/GG]GGGGATACCCTGAAG | 17970 |
rs243033535 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808736 | TGTTTGGGACAGGGT[G/T]TCTCTGTATAGCCCT | 17970 |
rs243106206 | in-del | -/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152824404 | CTTCGAGAAGACACG[-/C]CCCCCCAAGAAGACA | 17970 |
rs243151101 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152803888 | GTTGGTAACGTCAAC[C/T]ACCCTTAGAAAGAGT | 17970 |
rs243189561 | snp | C/G | | | utr-variant-5-prime, intron-variant | Ncf2 | Mm_Celera | 1:152807425 | ACCTGAATGGACACT[C/G]AAGATTCTCCATCCT | 17970 |
rs243253133 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812931 | TTTTCTTTTTTTAAA[G/T]ATTTATTTATTTATT | 17970 |
rs243253235 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806782 | GACAATACTCTCTCC[A/G]TAATGTAGAGTGCGG | 17970 |
rs243282501 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152829644 | TTGTATGTGACTAGA[A/C]TGTAGCTGTCTTCAG | 17970 |
rs243374255 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152803914 | AGAGTTTGGAGATGT[A/G]GATTGTTAGTGAAGC | 17970 |
rs243397481 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814559 | CAAACATCATACCAT[C/T]TACATCTTGATCTAT | 17970 |
rs243501253 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152831240 | GTCATCTTTAGCTAC[A/G]TGGCACTCTGATGAC | 17970 |
rs243538476 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152829232 | GCCTGGCGACTCACT[A/G]CGCTGGAGCCTCAAA | 17970 |
rs243607707 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152832982 | TTCACTTATACACAC[A/T]TTGCTGTGCTAACAT | 17970 |
rs243611038 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806067 | GCTGGACTTGGGAAA[A/G]AAGACGAGGTCATGG | 17970 |
rs243617426 | snp | A/G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152832506 | CACCACAAAGGAGCA[A/G/T]GGCTTGCCTCCGTGC | 17970 |
rs243655914 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808660 | CACACTGTAATTAAG[C/T]CATGAAGTTCACCAA | 17970 |
rs243687827 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814180 | TAAGCCATTTCTCCA[A/G]CCACCATGCTTGGCC | 17970 |
rs243718863 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826005 | CTGACAAACTGATCA[C/T]AGGGGTTCAGCCGCC | 17970 |
rs243752846 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813724 | GGATAGAGAGGAGAT[A/G]GATGTGGCCCATAGG | 17970 |
rs243919938 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826057 | GATCCCTACTCTCAG[C/T]CCTAGTTTACATGGC | 17970 |
rs243933456 | in-del | -/AC | | | intron-variant | Ncf2 | Mm_Celera | 1:152828066 | AAAGAAAAAAGAAAA[-/AC]AACCAAAATCCTTCT | 17970 |
rs243956748 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819222 | CCACACTTGGTTTCC[C/T]ACCATAAGCTTGTTT | 17970 |
rs243999922 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152828907 | GTTAGAGAGAGGGAG[A/G]GACAGGGTGATGGGA | 17970 |
rs244014513 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152818708 | CAACTTATGATGACA[A/G]GTTCTGTCCATATAT | 17970 |
rs244066136 | snp | A/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152800033 | CTACATAATCCAATC[A/T]TTTCTGTAACCTGCT | 17970 |
rs244210100 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806153 | GAAGGCTAGGTTGGG[G/T]AAGTCTCATGCACAG | 17970 |
rs244239553 | in-del | -/GCTGCT | | | intron-variant | Ncf2 | Mm_Celera | 1:152806294 | GCTGCTGCCGCTGCC[-/GCTGCT]GCTAAGGAGGAGGAG | 17970 |
rs244259376 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152834436 | GGCAACCCTGAGCTC[C/T]TCAAAAGCCTGTCTC | 17970 |
rs244284722 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152801903 | TTCTTGTTGTATTAA[C/G]ATTCAAATTGATTGG | 17970 |
rs244341608 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152817680 | TGCTGTAACCCGCCT[A/G]GGTACTTGATTAACA | 17970 |
rs244358470 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152825273 | TGAGGATGATACTTA[-/G]ATTAACCTGCAACCT | 17970 |
rs244397091 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815508 | AAACGCCAAGTAAAA[A/G]TACTCTGGAGCCAAG | 17970 |
rs244398560 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152809340 | TGACCAAGAAGCAAA[C/T]TGGGGAGGAAAGGGT | 17970 |
rs244426474 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152824545 | CATCACTCACTCCTG[A/T]GGTTTCTACTGGGAT | 17970 |
rs244518360 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152828692 | GCCAAATATCCTCCC[A/C]ACCCCCCTTGTCTGA | 17970 |
rs244662931 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152800571 | TGTGACCAGCTGCTT[C/T]AGGGTCTGACACCAT | 17970 |
rs244701491 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798158 | CCAGCCTGGTCTACA[A/G]AGTGAGTTCCAGGAC | 17970 |
rs244710383 | snp | A/C | | | utr-variant-3-prime | Ncf2 | Mm_Celera | 1:152836165 | CTTGCAAGACTTACC[A/C]ATCTCTGCTGTGCGC | 17970 |
rs244789672 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816394 | AGGGGACCAGACAGC[C/T]ACACACAGCCTGTGC | 17970 |
rs244815518 | snp | A/G/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798407 | CAGGAAATGGGTCAG[A/G/T]ATGGTTGCTCACCCC | 17970 |
rs244932165 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152803360 | GCACATGCATTGCAG[G/T]CATGCAGAATGGTGG | 17970 |
rs244939454 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152834852 | GGTTTATTATGTAAG[G/T]CAATTTAAAGCTACA | 17970 |
rs245032713 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152810059 | CCCCCATCCAGCCTC[C/T]GCCTGGAGGGAGGAA | 17970 |
rs245085517 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152821817 | TGGAACAGTACAGCC[C/T]CTGAATCTCTTCTAG | 17970 |
rs245103649 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152822880 | ACTGAGGTGAAGATT[A/G]GGGTTGTCAGATCTG | 17970 |
rs245121067 | snp | A/G | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800478 | TGAAAAGTGACCAGG[A/G]CTTGGGTCCTCCCTG | 17970 |
rs245140168 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804870 | AGATGTGATATGACT[G/T]AACCCTCACGCTGAC | 17970 |
rs245161920 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152805042 | GACCCACAGGCTGTC[A/G]GAGGGAACTGTGTGC | 17970 |
rs245162564 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804325 | ATTCTTTCTTTGTGG[C/T]TGCAAACCGCAGCCT | 17970 |
rs245195672 | in-del | -/TGTT | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813430 | TAGATCCCCAGGATC[-/TGTT]TGTCTCTGCATCCCC | 17970 |