SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13468067 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Ncf4 | Mm_Celera | 15:78250448 | CATCGAGGAGAAGAG[A/G]GGCTTCACCAGCCAC | 17972 |
rs31520004 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Ncf4 | Mm_Celera | 15:78244225 | CCGCAGGAAAAGCCC[A/G]GAGAGTGGCAGGGAG | 17972 |
rs31520005 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Ncf4 | Mm_Celera | 15:78244314 | AGATAGGAGAGGAGC[A/G]TTGGGAATGTGGTGG | 17972 |
rs31520006 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Ncf4 | Mm_Celera | 15:78244504 | ATGTGGTATCTCAGA[A/G]CCCAGAGCCCCAGAT | 17972 |
rs31520007 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Ncf4 | Mm_Celera | 15:78244769 | TCCCCAAAGCCAGTG[G/T]CCTCACGCAAGCCCA | 17972 |
rs31520008 | snp | C/T | 0.231111 | 0.249285 | utr-variant-5-prime, intron-variant | Ncf4 | Mm_Celera | 15:78244861 | GAGGGCCAGGCAGCT[C/T]AAAGCCTGAAGGAGG | 17972 |
rs31520009 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ncf4 | Mm_Celera | 15:78245484 | CCTTCAGACTGAAAC[G/T]GGCCTCTGCGTTTTC | 17972 |
rs31520010 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ncf4 | Mm_Celera | 15:78245502 | CCTCTGCGTTTTCCT[A/G]TCTTTAGGTTCAGAT | 17972 |
rs31520011 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf4 | Mm_Celera | 15:78245532 | TAGCCCAGGCTCTGC[C/T]GTCTGACCCCTCACT | 17972 |
rs31520012 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ncf4 | Mm_Celera | 15:78245574 | TCCTGAACAGGTCTT[A/G]GATGCTTGGCACAAT | 17972 |
rs31520013 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf4 | Mm_Celera | 15:78245606 | TTGGGGGCCGGGTCT[C/T]TGCTCTGCCTGCTCT | 17972 |
rs31520204 | snp | A/G | 0.32 | 0.24 | intron-variant | Ncf4 | Mm_Celera | 15:78249907 | GGCAGAGTAAACCAG[A/G]TGCAAGCAGAGGAGC | 17972 |
rs31520206 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ncf4 | Mm_Celera | 15:78249927 | AGCAGAGGAGCTGGA[A/G]AAGAACATGGTCCCT | 17972 |
rs31520207 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ncf4 | Mm_Celera | 15:78250322 | TGCAGGCCTCCATCA[C/G]CTGGCTGTGTCCAGA | 17972 |
rs31520209 | snp | C/T | 0.32 | 0.24 | intron-variant | Ncf4 | Mm_Celera | 15:78250333 | ATCAGCTGGCTGTGT[C/T]CAGAGCAGGCAAGGT | 17972 |
rs31520212 | snp | C/T | 0.32 | 0.24 | intron-variant | Ncf4 | Mm_Celera | 15:78250507 | TTGACCTCGAACCTC[C/T]AATCTTCCACCTTGA | 17972 |
rs31520864 | snp | A/C | 0.32 | 0.24 | intron-variant | Ncf4 | Mm_Celera | 15:78245697 | CACACTGAGAGCTCA[A/C]TACATCTGCTAAGAG | 17972 |
rs31520865 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf4 | Mm_Celera | 15:78245752 | TGGACAATGCTGACA[C/T]TATACAGGTAGGGAC | 17972 |
rs31520866 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Ncf4 | Mm_Celera | 15:78245813 | CCTCATTCAGTCAGC[A/C]CTTGCTCAGTGTCTC | 17972 |
rs31520867 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ncf4 | Mm_Celera | 15:78245837 | GTGTCTCTTATGGAG[A/C]CAGCCCTGTGTTCCC | 17972 |
rs31520868 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf4 | Mm_Celera | 15:78245869 | TCTGCATGTGGAGAC[C/T]CAAATGACAGAACCG | 17972 |
rs31520869 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ncf4 | Mm_Celera | 15:78245932 | AGCCAAGTGTCCATG[G/T]GAACTGCTTGAGAGT | 17972 |
rs31520870 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ncf4 | Mm_Celera | 15:78245965 | CCAGAACAGGTCTGA[C/T]TGACAAGACCCAGGT | 17972 |
rs31520871 | snp | A/G | 0.32 | 0.24 | intron-variant | Ncf4 | Mm_Celera | 15:78246251 | CTTGTTTCTTGGGGT[A/G]CAGAGTTCAGATGGT | 17972 |
rs31520872 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Ncf4 | Mm_Celera | 15:78246485 | ATATAGTGTCTCTTC[C/G]AGGGCAGCTGCAGAG | 17972 |
rs31521344 | snp | C/T | 0.32 | 0.24 | intron-variant | Ncf4 | Mm_Celera | 15:78250614 | GCATGGGACACCACA[C/T]TGAAGGCTTACCCCA | 17972 |
rs31521346 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ncf4 | Mm_Celera | 15:78251041 | CTCTGTCCAACGCCC[A/G]GAGCTGGCCCTGACC | 17972 |
rs31521348 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Ncf4 | Mm_Celera | 15:78252373 | GCCTGCTGAAAGGAA[A/C]CTTACAGAGCCCTCC | 17972 |
rs31521350 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ncf4 | Mm_Celera | 15:78253058 | TCCTTCTGCCTTCTC[C/G]TGATGGTATGATGGG | 17972 |
rs31521352 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Ncf4 | Mm_Celera | 15:78253678 | GCACCCTGTCAACAG[A/T]AGCATCCAAGCCATG | 17972 |
rs31521754 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Ncf4 | Mm_Celera | 15:78246492 | GTCTCTTCCAGGGCA[C/G]CTGCAGAGTTTAGCT | 17972 |
rs31521756 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ncf4 | Mm_Celera | 15:78246577 | CAGTTTTCAGGACTC[A/C]CCTAGATCAGGTCCC | 17972 |
rs31521758 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Ncf4 | Mm_Celera | 15:78246599 | TCAGGTCCCCAAGCG[G/T]ACCTCCATGTGTAGC | 17972 |
rs31521759 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Ncf4 | Mm_Celera | 15:78246626 | TAGCTCCCGTGTGCA[C/T]GGAGCCTGGTATCCA | 17972 |
rs31521760 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ncf4 | Mm_Celera | 15:78246627 | AGCTCCCGTGTGCAC[A/G]GAGCCTGGTATCCAC | 17972 |
rs31521762 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Ncf4 | Mm_Celera | 15:78246797 | TAGGCGCCTGGCGCC[G/T]CTCTGGGTGCTTAGG | 17972 |
rs31522264 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ncf4 | Mm_Celera | 15:78254918 | CACGCGCAAAATGTA[A/G]GTGGCCATCCCTGCA | 17972 |
rs31522266 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Ncf4 | Mm_Celera | 15:78255249 | TGGAGACTTAAGGGC[A/G]CTGAGCCGTGATCCC | 17972 |
rs31522268 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Ncf4 | Mm_Celera | 15:78255961 | ACTGGGAACAGCAAA[C/T]TGGAGCTAAGTTTCA | 17972 |
rs31522269 | snp | C/T | 0.5 | 0 | intron-variant | Ncf4 | Mm_Celera | 15:78257752 | ATGTTACTTCCCTAA[C/T]CAGCAGCAAGGATGA | 17972 |
rs31522271 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ncf4 | Mm_Celera | 15:78257941 | GGTTTCCTTTCCTGT[A/G]AATGATGAAAACAGT | 17972 |
rs31522273 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Ncf4 | Mm_Celera | 15:78259672 | CATATAAATATAGAT[A/G]CCAAAAAGAATGCAT | 17972 |
rs31522624 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ncf4 | Mm_Celera | 15:78246984 | CCTGTCTGGCCTAGT[A/T]TGTCTTCTGACACTA | 17972 |
rs31522626 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ncf4 | Mm_Celera | 15:78247026 | ACACTTCTGGTTTCT[C/T]CTACCCCAGAGAAAG | 17972 |
rs31522628 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ncf4 | Mm_Celera | 15:78247102 | GTCTGCTTCTGGCCT[C/G]TTTTCCCTTGCTCTG | 17972 |
rs31522629 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ncf4 | Mm_Celera | 15:78247137 | CTGTCCTGCCTCTGA[C/T]CATGCCTGCCTTCCT | 17972 |
rs31522631 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ncf4 | Mm_Celera | 15:78247160 | GCCTTCCTGAAGTTT[A/C]TTGAAATTGTCCCTC | 17972 |
rs31522633 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ncf4 | Mm_Celera | 15:78247240 | GATAGGACCTCCCTG[C/G]TGCCGTAGCCGGCTC | 17972 |
rs31523235 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Ncf4 | Mm_Celera | 15:78260150 | ACTAGAGTGCAGGTC[G/T]CTGGGTTAGGCAGCC | 17972 |
rs31523237 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Ncf4 | Mm_Celera | 15:78260590 | ACTCTGAGACGTGAC[A/C]CTGGGTCTCACCAGC | 17972 |
rs31523239 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Ncf4 | Mm_Celera | 15:78262024 | CAAGAAGCTTCAGGC[C/T]GTACCATTATTGGAT | 17972 |
rs31523240 | snp | A/G | 0.188366 | 0.242283 | intron-variant, missense | Ncf4 | Mm_Celera | 15:78262111 | AGGCTGTTGGATGAT[A/G]GGCCCCGGTACCACT | 17972 |
rs31523242 | snp | C/T | 0.359862 | 0.224567 | synonymous-codon, downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262220 | CCAGAGAGAAGACAT[C/T]GCCCTTAGCTACCAG | 17972 |
rs31523575 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Ncf4 | Mm_Celera | 15:78247245 | GACCTCCCTGGTGCC[A/G]TAGCCGGCTCTCTGT | 17972 |
rs31523577 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ncf4 | Mm_Celera | 15:78247251 | CCTGGTGCCGTAGCC[A/G]GCTCTCTGTGCTTTC | 17972 |
rs31523579 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ncf4 | Mm_Celera | 15:78247371 | TGGTGTCTTGAAGAA[C/T]GTGATGAGGGTCACC | 17972 |
rs31523581 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Ncf4 | Mm_Celera | 15:78247378 | TTGAAGAACGTGATG[A/C]GGGTCACCCGTGGAA | 17972 |
rs31523583 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ncf4 | Mm_Celera | 15:78247387 | GTGATGAGGGTCACC[C/T]GTGGAAAGTCCTTGG | 17972 |
rs31524144 | snp | C/T | 0.484429 | 0.0868505 | utr-variant-3-prime, downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262442 | GCAAAGGGCCTTTAC[C/T]TTCCAAGAACACGGA | 17972 |
rs31524146 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262536 | TCTATTAAGTTTTTG[A/G]CACTCTACCTTTTGG | 17972 |
rs31524148 | snp | A/G | 0.244898 | 0.249948 | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262653 | ACCTCTTACCTTTCT[A/G]AACGACGTTATGGGG | 17972 |
rs31524149 | snp | C/T | 0.244898 | 0.249948 | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262735 | TCTAAAAGTGCACAG[C/T]AGGGAGAAAAGAGTC | 17972 |
rs31524445 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ncf4 | Mm_Celera | 15:78247492 | CAGAGAGCAGGACCC[C/T]GTGATGCTAAGAAGT | 17972 |
rs31524447 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ncf4 | Mm_Celera | 15:78247504 | CCCCGTGATGCTAAG[A/T]AGTGTCTGTTCTGTG | 17972 |
rs31524449 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ncf4 | Mm_Celera | 15:78247524 | TCTGTTCTGTGCTCC[A/G]GGCTGCAGAATGCGG | 17972 |
rs31524450 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ncf4 | Mm_Celera | 15:78247536 | TCCGGGCTGCAGAAT[A/G]CGGGGAACAGGCCCA | 17972 |
rs31524452 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ncf4 | Mm_Celera | 15:78247611 | CCCACTCACCTCACC[C/T]GGGCAAGCTCCATAA | 17972 |
rs31525324 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ncf4 | Mm_Celera | 15:78247632 | AGCTCCATAACCTCT[C/T]GGTGCCTCACCATCA | 17972 |
rs31525326 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ncf4 | Mm_Celera | 15:78247687 | CCAAGGAGTAGGTGC[C/T]CAGTTCCTGGTGTGG | 17972 |
rs31525327 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ncf4 | Mm_Celera | 15:78247702 | CCAGTTCCTGGTGTG[C/G]TGTGAGCACTCTCAG | 17972 |
rs31525329 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf4 | Mm_Celera | 15:78247857 | GGACATGTTGAAAAG[C/T]GAGTGGGAAGGCCCC | 17972 |
rs31525331 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ncf4 | Mm_Celera | 15:78248070 | GTGAGGTGTGGGACA[A/T]GTCCTATCTGTCTCT | 17972 |
rs31525332 | snp | A/G | 0.5 | 0 | intron-variant | Ncf4 | Mm_Celera | 15:78248674 | CACTTAAGGGTCTTA[A/G]GTCTTAGCCACAGCC | 17972 |
rs31526234 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ncf4 | Mm_Celera | 15:78248685 | CTTAAGTCTTAGCCA[C/T]AGCCATAAGCCACAG | 17972 |
rs31526235 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Ncf4 | Mm_Celera | 15:78248862 | AGGCATCACTCTTGT[C/T]GTGGCTCTTTCTTTC | 17972 |
rs31526237 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf4 | Mm_Celera | 15:78248887 | TCTTTCAGTCCAGGT[C/T]GGCTGCTATACCTTG | 17972 |
rs31526239 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ncf4 | Mm_Celera | 15:78248930 | TTGGAAATGCATTAG[A/G]CTGCAGGGAAAGGCT | 17972 |
rs31526240 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf4 | Mm_Celera | 15:78249395 | ATCACCCTTCACTGT[C/T]GGAGCTTCTCATGGA | 17972 |
rs31526241 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ncf4 | Mm_Celera | 15:78249408 | GTCGGAGCTTCTCAT[A/G]GAGCTGTCTCATTAA | 17972 |
rs31526243 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ncf4 | Mm_Celera | 15:78249531 | CCTTAAGACCCACCA[C/G]GCTCTCAGCAAATCT | 17972 |
rs31526566 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242466 | CTTGTGACGTCACCA[C/T]TCTCCGAGTCAGAGG | 17972 |
rs31526567 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242768 | TTCTCTTGTGGAAGC[A/G]ATGTCACCATTTCCT | 17972 |
rs31526568 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243010 | GGATTTGCAGTTTTG[C/T]GTAGTGCTGACTCCG | 17972 |
rs31526569 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243029 | GTGCTGACTCCGAAC[C/T]GCTTCCTCAGCACAG | 17972 |
rs31526570 | snp | A/G | 0.475309 | 0.108333 | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243115 | TCCCTCTGTCTACCC[A/G]TGGCTGGAGAACTTC | 17972 |
rs31526571 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243133 | GCTGGAGAACTTCCT[C/T]CGCTTCCTCGGGCAC | 17972 |
rs31526572 | snp | C/T | 0.188366 | 0.242283 | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243176 | CTGAGAAACCCTCTT[C/T]GGTGTTTGCTGTGAT | 17972 |
rs31526573 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243308 | ACACATGTGTTTGCC[A/G]TTCCCTAGGCCTGGG | 17972 |
rs31527285 | snp | A/C | 0.32 | 0.24 | intron-variant | Ncf4 | Mm_Celera | 15:78249693 | TTGGGCATAGTCAAC[A/C]AACCGATCTCTTGGC | 17972 |
rs31527287 | snp | A/G | 0.32 | 0.24 | intron-variant | Ncf4 | Mm_Celera | 15:78249782 | AGTCAATTAATATAT[A/G]AAGTAAAAAGGTTTA | 17972 |
rs31527288 | snp | A/G | 0.32 | 0.24 | intron-variant | Ncf4 | Mm_Celera | 15:78249824 | GGTTCCATGGATCCC[A/G]CCTAAAAGCACGGCA | 17972 |
rs31527289 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ncf4 | Mm_Celera | 15:78249835 | TCCCGCCTAAAAGCA[C/T]GGCAACCCCTTTGCC | 17972 |
rs31527290 | snp | A/G | 0.32 | 0.24 | intron-variant | Ncf4 | Mm_Celera | 15:78249884 | AGTGAAGTGAAGCAG[A/G]AGTGCATGGCAGAGT | 17972 |
rs31527474 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243319 | TGCCGTTCCCTAGGC[C/T]TGGGTATCAGTCTCC | 17972 |
rs31527475 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243493 | ATTCTACGTTCCTCT[A/G]CCACCCTGATCTATC | 17972 |
rs31527476 | snp | C/G | 0.124444 | 0.216185 | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243856 | GTGAGAAACATAGGC[C/G]GTTCCAGATTCCTCA | 17972 |
rs31527477 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78244048 | TGTAGGCTTTGGAGA[A/G]CTCCCTACAGAACCA | 17972 |
rs31527478 | snp | A/C | 0.391111 | 0.206368 | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78244061 | GAGCTCCCTACAGAA[A/C]CAAGCATTAGAAGGA | 17972 |
rs31527479 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78244079 | AGCATTAGAAGGAGC[C/T]GACGAAGAACTTCCT | 17972 |
rs31527480 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78244126 | TCTGGGTGTCCGCAG[C/T]GTAGTGCTGGCCTGG | 17972 |
rs31527481 | snp | A/G/T | 0.35503 | 0.226867 | upstream-variant-2KB, intron-variant | Ncf4 | GRCm38.p3 | 15:78244195 | GGGGTAGGGAACCCC[A/G/T]CTGGTGAGAGCTTGC | 17972 |
rs31551042 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ncf4 | Mm_Celera | 15:78252730 | GTATACTATATGTGT[A/G]TGTGGTGCATATATA | 17972 |
rs31575973 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ncf4 | Mm_Celera | 15:78257835 | CCTAGTGTGCAAGGC[C/T]CTGGGTCCCACTCAC | 17972 |
rs31586117 | snp | C/G | 0.5 | 0 | intron-variant | Ncf4 | Mm_Celera | 15:78247314 | CATGGCAATCCTAAC[C/G]TCCCCACCCCCACCC | 17972 |
rs31587929 | snp | A/G | 0.32 | 0.24 | intron-variant | Ncf4 | Mm_Celera | 15:78255373 | AGAGCAACCAACCAT[A/G]ACTGGTGGCTGCGCA | 17972 |
rs31596963 | snp | A/C | 0.444444 | 0.157135 | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78263059 | CTAAAAGACAGAAAG[A/C]AACTGCCTTGTAGTT | 17972 |
rs31648461 | snp | C/G | 0.444444 | 0.157135 | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262589 | TAAGGGCCACAGTTG[C/G]GAAATGGGATTTTGT | 17972 |
rs31653179 | snp | A/G | 0.5 | 0 | intron-variant | Ncf4 | Mm_Celera | 15:78258958 | CCCCCCACATCAATC[A/G]TTAATAATAATAATA | 17972 |
rs31704358 | snp | A/G | 0.444444 | 0.157135 | missense | Ncf4 | Mm_Celera | 15:78250998 | GCCCTTTCACCTGCA[A/G]CCTGCCCACATTGCC | 17972 |
rs31716629 | snp | A/G | 0.5 | 0 | intron-variant | Ncf4 | Mm_Celera | 15:78257551 | GGGGTCGTGGAGACA[A/G]ATAATTCCTGGGAAA | 17972 |
rs31740335 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ncf4 | Mm_Celera | 15:78252160 | TCACAGGTGCCCACC[C/T]TTCCTGCCCTATTGC | 17972 |
rs31822735 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ncf4 | Mm_Celera | 15:78252603 | CTGTGTGCATTTGTG[C/T]ATATACATATACATA | 17972 |
rs31888785 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ncf4 | Mm_Celera | 15:78254765 | CTTTTCGTCGACTGC[C/T]CACCTGTCCCTCCTC | 17972 |
rs31892056 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ncf4 | Mm_Celera | 15:78251867 | CCCTGTCTGATGAGC[A/G]TTAACCAAGCAGCGC | 17972 |
rs32005373 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ncf4 | Mm_Celera | 15:78261977 | CCTTGCTTTCTCTTA[A/G]GAAACTCCTAAACCT | 17972 |
rs32008427 | snp | G/T | 0.444444 | 0.157135 | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262975 | CTGGCCTGTGGAGAT[G/T]CAAGGCCAGGCAGTT | 17972 |
rs32023903 | snp | A/G | 0.32 | 0.24 | intron-variant | Ncf4 | Mm_Celera | 15:78255377 | CAACCAACCATAACT[A/G]GTGGCTGCGCATAAT | 17972 |
rs32028298 | snp | C/T | 0.32 | 0.24 | intron-variant | Ncf4 | Mm_Celera | 15:78255611 | GCACAGCATGAAATG[C/T]CATGGCAAAGAACAG | 17972 |
rs32041411 | snp | A/G/T | 0.5 | 0 | intron-variant | Ncf4 | GRCm38.p3 | 15:78253901 | CTCTATTGAGAAAAT[A/G/T]AAGGGAAGGGGGTTT | 17972 |
rs32078493 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ncf4 | Mm_Celera | 15:78255407 | TCTTTCTCTCCCTGC[A/C]TCTCCAGGGACCCAC | 17972 |
rs32107730 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262660 | ACCTTTCTAAACGAC[A/G]TTATGGGGAACATAG | 17972 |
rs32120381 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242682 | TGCTCTGCATCCCAG[C/T]CCCAAACCAGCACAT | 17972 |
rs32124704 | snp | A/C | 0.5 | 0 | intron-variant | Ncf4 | Mm_Celera | 15:78250828 | CCCCCCCACCCCGTT[A/C]TAGCTCCCCTCCCCC | 17972 |
rs32182048 | snp | A/G | 0.5 | 0 | intron-variant | Ncf4 | Mm_Celera | 15:78252989 | TGCATACATATGAGT[A/G]TGTGTGTACCTGTAC | 17972 |
rs32208706 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ncf4 | Mm_Celera | 15:78261711 | GTCCCCCTGGCCATA[G/T]CTACCATTCTCAAGA | 17972 |
rs32240494 | snp | C/T | 0.5 | 0 | intron-variant | Ncf4 | Mm_Celera | 15:78250580 | TAGAATTCAGCGGTG[C/T]TTCTAAACACATCCA | 17972 |
rs32326353 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime, downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262421 | GTGGCAAGGACGGGG[C/T]GCTCAGCAAAGGGCC | 17972 |
rs32331094 | snp | C/T | 0.32 | 0.24 | intron-variant | Ncf4 | Mm_Celera | 15:78253459 | TTCCTGAGGCCTCCA[C/T]GATCCCATCTTCAAT | 17972 |
rs32352153 | snp | C/T | 0.32 | 0.24 | intron-variant | Ncf4 | Mm_Celera | 15:78253445 | TGAAAACTGACATTT[C/T]CCTGAGGCCTCCACG | 17972 |
rs32384999 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ncf4 | Mm_Celera | 15:78251880 | GCGTTAACCAAGCAG[C/T]GCTGTGGGGAGCCTC | 17972 |
rs32395073 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78263039 | AGAGTACCACAAAAT[A/G]GAGACTAAAAGACAG | 17972 |
rs32440250 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ncf4 | Mm_Celera | 15:78261461 | ACATTCACACACACA[A/C]AAAAAACAAACACAC | 17972 |
rs32529598 | snp | C/T | 0.5 | 0 | intron-variant | Ncf4 | Mm_Celera | 15:78250554 | CTGGGTGGTTGCTGA[C/T]ATTTGCTGGATAGAA | 17972 |
rs32531327 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ncf4 | Mm_Celera | 15:78259698 | TGCATCTTCTGTCTC[A/G]TGACCATGGAGGTTT | 17972 |
rs32537022 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ncf4 | Mm_Celera | 15:78259701 | ATCTTCTGTCTCGTG[A/G]CCATGGAGGTTTTAA | 17972 |
rs33858784 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ncf4 | Mm_Celera | 15:78261443 | GCACACTAACACACA[A/G]ACACATTCACACACA | 17972 |
rs50463490 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Ncf4 | Mm_Celera | 15:78244166 | AACACACAAACACAC[A/G]TTTGGAACACACTGG | 17972 |
rs50868866 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78257159 | AAGGCAGAGGCAAGG[G/T]TAGAAGAAAGGTATT | 17972 |
rs50880908 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Ncf4 | Mm_Celera | 15:78244168 | CACACAAACACACGT[C/T]TGGAACACACTGGGG | 17972 |
rs52265471 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78261617 | AAAACAAACATGTAC[A/G]CAGAAACACAAATAT | 17972 |
rs107663081 | snp | A/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243931 | ATAGGAGCCTGATTC[A/G]GGCAGGCTGGGCAGG | 17972 |
rs107664495 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78248512 | TCAGCCTCTTCATTT[C/T]TGAGATCACAGACAT | 17972 |
rs107698384 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78245321 | CCAGTAAGAAGCCTA[A/C]GGCTCAGAATGGGGA | 17972 |
rs107707734 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78247193 | ATACGATTTCCAGGG[A/G]GTCTTTGTGCTGTCC | 17972 |
rs107735900 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78245356 | CTTGGATGTGGCCAA[A/G]GACCACAGGGTGAGT | 17972 |
rs107777882 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78258877 | ACTCTCCATGGCTTG[C/T]TCAGACTGCTTTCTT | 17972 |
rs107778630 | snp | A/C | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243904 | CCACAGCCACGTTCC[A/C]AAGTTGGGGAGATAG | 17972 |
rs107781843 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78249579 | TCAGAACCTTAGCAC[A/G]AGCCATTTCCACTAC | 17972 |
rs107788077 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78246011 | GTGGGATCTGGAAAA[A/G]GGGATGGGATTCCTG | 17972 |
rs107800310 | snp | A/C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78250819 | CCGGTATATCCCCCC[A/C/T]ACCCCGTTCTAGCTC | 17972 |
rs107830686 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78247658 | CATCACCCTACCCCA[A/G]GGTGGCTCTATCTCC | 17972 |
rs107865950 | snp | G/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243995 | AAGTGGAGCTGGGGG[G/T]TGGGGGACATTCTCT | 17972 |
rs107894509 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78246716 | TCCCCACACCACAGC[C/T]TCCTTGGCAGCTCAG | 17972 |
rs107917256 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78250356 | GGCAAGGTGGTAACC[A/G]ATCCCCTCCCTCTGG | 17972 |
rs107925663 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78246666 | ACCCGTGTGGGGTCC[A/G]AGGGGGACAGCTATC | 17972 |
rs107928135 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78245358 | TGGATGTGGCCAAGG[A/G]CCACAGGGTGAGTGG | 17972 |
rs107973259 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78246712 | CCTCTCCCCACACCA[C/T]AGCCTCCTTGGCAGC | 17972 |
rs107973435 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78246349 | GCCCTCTGAGGGGGG[C/T]GGCTCTCCTCCTCTG | 17972 |
rs107989558 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78245672 | TCTGGGAGGCCGAAC[A/G]GCCCTGGGACACACT | 17972 |
rs108007386 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252333 | TGTGAGTGGGGCTTG[G/T]AGCTCATGGTTTCTA | 17972 |
rs108075846 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78254754 | GCTGTCTAGATCTTT[C/T]CGTCGACTGCCCACC | 17972 |
rs108082683 | snp | G/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243802 | TTGGAGCCAGATCCT[G/T]AGGAGTCTGAGACTG | 17972 |
rs108119274 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78261078 | CTTTGGAGGGCAATG[C/G]GCTAGGAGGGGACCT | 17972 |
rs108124553 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78248039 | GGTGTGTGGGCTCCT[A/G]GGGATCCCATACTTT | 17972 |
rs108125067 | snp | A/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78245336 | AGGCTCAGAATGGGG[A/T]GTGGCTTGGATGTGG | 17972 |
rs108159453 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78246684 | GGGGACAGCTATCTT[C/T]CCAGTCCCCTTCCCT | 17972 |
rs108203845 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78248738 | ACACGTCAGCCCCAC[C/T]CTGCCATCTCCACAC | 17972 |
rs108246499 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78249292 | AAAAAAACAACAACA[A/G]CAACAAAACACCAAA | 17972 |
rs108317887 | snp | A/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243801 | CTTGGAGCCAGATCC[A/T]GAGGAGTCTGAGACT | 17972 |
rs108367055 | snp | C/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243374 | TGCTCGTCTTAGACC[C/T]CTCAGATCACCTTTC | 17972 |
rs108381390 | snp | C/T | | | utr-variant-5-prime, intron-variant | Ncf4 | Mm_Celera | 15:78244935 | CTCAAAGGCTGCCCC[C/T]GGGGACACCCCAAGC | 17972 |
rs108409111 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78258284 | GATATAACACTTTGA[G/T]CTTCTGCCTCCTTGT | 17972 |
rs108434372 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78246356 | GAGGGGGGTGGCTCT[C/T]CTCCTCTGCCCCTGA | 17972 |
rs108455402 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78254442 | CTCTGGATGCCCCAG[C/T]TGTGTTACTAAGCTG | 17972 |
rs108504991 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78245375 | CACAGGGTGAGTGGG[C/T]GGCAGAGCCTGGGAG | 17972 |
rs108531923 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78246140 | GCTGCATAATATGAC[C/T]CCAGCCTTTCTCACC | 17972 |
rs108532280 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78248040 | GTGTGTGGGCTCCTG[A/G]GGATCCCATACTTTG | 17972 |
rs108538827 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78245892 | CAGAACCGTCCCCTG[A/G]ATCAAGCAGAAAGCA | 17972 |
rs108561204 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78245311 | GTGTTATGCACCAGT[A/G]AGAAGCCTAAGGCTC | 17972 |
rs108567819 | snp | A/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78246219 | GAAACTGTAGCCACT[A/T]GAAGCTTGGGTCCCT | 17972 |
rs108605995 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78257434 | GCACCCTCTTTATCC[A/C]CTGAGCCATTTCACA | 17972 |
rs108674832 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78245160 | GGGTGGGTATGGGGA[A/G]GTAAGAGGCTGTCCC | 17972 |
rs108714116 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78250537 | ACAGTGGTTTCTCTG[A/G]ACTGGGTGGTTGCTG | 17972 |
rs108818535 | snp | A/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242589 | CTCCACGTCCTGAGA[A/G]CTGGGATTACATGTG | 17972 |
rs108828215 | snp | A/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243879 | ATTCCTCAGGGGGAA[A/G]GCCCTGTCCCCACAG | 17972 |
rs108873745 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78249667 | TCCACCTTTCTGAAG[C/T]TTTTCCTTACTTGGG | 17972 |
rs211707202 | snp | G/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242191 | TTGTGTGTGTGTGCA[G/T]TGTGTGCATGTGTGT | 17972 |
rs211910359 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78255758 | AAAGGACCACCCACT[C/T]TGTAGTTGGGGGAGA | 17972 |
rs212081003 | snp | A/G | | | missense | Ncf4 | Mm_Celera | 15:78250413 | CCAGACGATGTGGCC[A/G]TCTCAGCCAACATCG | 17972 |
rs212450482 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78258087 | TGTGACCCTGAAGCT[A/G]GGCCCCCTTGGGTGT | 17972 |
rs212452984 | snp | A/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78244004 | TGGGGGTTGGGGGAC[A/T]TTCTCTGGGCTGCTG | 17972 |
rs212605730 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78259690 | AAAAAGAATGCATCT[G/T]CTGTCTCATGACCAT | 17972 |
rs212667300 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78260165 | TCTGGGTTAGGCAGC[C/T]TGGTGAATCTCCTCA | 17972 |
rs213137049 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78252459 | AAAAGCTCCTATGGT[A/G]ACCTGAGTGTTATCC | 17972 |
rs213199410 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78252915 | GGCTTATGCATGTCT[A/G]AGCTTTGCATGGGTA | 17972 |
rs213370480 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78247560 | AGGCCCAGTGCTGGG[C/T]TTCATCCAAGGTCTC | 17972 |
rs213599308 | in-del | -/A | | | intron-variant | Ncf4 | Mm_Celera | 15:78258987 | AATAGTAATAGTAAT[-/A]AATACTCCAAGGACT | 17972 |
rs213629068 | snp | A/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78253743 | CCTTTACAGCTGGAG[A/T]GCTCTGGCTTTGGAG | 17972 |
rs213661524 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78261520 | AAATGAGCACAAACA[C/T]ACAGTGTACACACAA | 17972 |
rs213726435 | in-del | -/TT | | | intron-variant | Ncf4 | Mm_Celera | 15:78261440 | AGGCACACTAACACA[-/TT]CAAACACATTCACAC | 17972 |
rs213759493 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78256092 | AGAAGGAGGGTGATG[G/T]CAGAGTACATGGATG | 17972 |
rs213816438 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78257308 | TGATCCAGATGTGTT[A/G]GTGAAGCAGAACATT | 17972 |
rs213832752 | snp | C/T | | | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262908 | CCTGTGGCTCCTGGT[C/T]CCCTGTACAATGGGT | 17972 |
rs214180258 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78261988 | CTTAGGAAACTCCTA[A/G]ACCTTCCACCCACTT | 17972 |
rs214306184 | snp | A/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78250298 | ATGGACAGTGTTCAG[A/T]ATGGGGTGTGCAGGC | 17972 |
rs214318620 | in-del | -/GCT | | | intron-variant | Ncf4 | Mm_Celera | 15:78248119 | CCAATCACTTCTTCA[-/GCT]ACTCCTCCTCCTCAC | 17972 |
rs214764433 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78251368 | AGGGTGGCTCTCCAG[C/T]CACACAGCCTCAGCC | 17972 |
rs214918351 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252558 | TTTTATGCAAGTGTA[C/T]GTATTTTTGTGTGTT | 17972 |
rs215100533 | snp | C/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243229 | AAGGTGGACTTCCTG[C/T]CAGCAGTGGGACATG | 17972 |
rs215174777 | in-del | -/TCC | | | intron-variant | Ncf4 | Mm_Celera | 15:78248296 | CTCTTCCTCCTCTCT[-/TCC]TCCTCCTCCTCCTTT | 17972 |
rs215185948 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78259615 | AAGTGCATGTATGTA[C/T]TTACACACATACAAA | 17972 |
rs215339472 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78260868 | CCCTGCAGCTGCTGC[G/T]GTGGCTCCCAGATAA | 17972 |
rs215413116 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252971 | AGCATGTATGTGTGT[G/T]CATGCATACATATGA | 17972 |
rs215544315 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78259054 | CTGAGGTTCCCTCTT[C/T]CTAGACAACTCTCTT | 17972 |
rs215575407 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78248544 | TGCCACCTATGCCTG[C/G]CTACACCCACTTCCT | 17972 |
rs215735573 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78260298 | CTCCAATTCCTGCGC[C/T]GAGGTCCTGCATCCT | 17972 |
rs215879105 | in-del | -/ACG | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243897 | CCTGTCCCCACAGCC[-/ACG]TTCCAAAGTTGGGGA | 17972 |
rs216151711 | in-del | -/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242191 | TGTGTGTGTGTGCAT[-/G]TGTGTGCATGTGTGT | 17972 |
rs216399725 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78261624 | ACATGTACACAGAAA[C/T]ACAAATATACGTAAA | 17972 |
rs216450523 | in-del | -/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78251635 | TCTGTGGGTGTGCTG[-/T]TCCCCCAAACACATT | 17972 |
rs216506376 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78262043 | CCATTATTGGATTAC[C/T]CAGTGTCCTCTTCCT | 17972 |
rs216519204 | snp | C/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243352 | CCTCAGTCATGGGTA[C/T]AATTCCTGCTCGTCT | 17972 |
rs216580907 | snp | A/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243982 | TTAGCATACCATCAA[A/G]TGGAGCTGGGGGTTG | 17972 |
rs216745536 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78257364 | AGCTTGCAGAAGTTG[A/G]CCCTCTCCTGTCAGG | 17972 |
rs216894627 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78259638 | CATACAAATACATAA[A/G]TATACACATGCCCAC | 17972 |
rs217071418 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78261494 | ACCAATACACACCCA[A/C]AACATATAACAAATG | 17972 |
rs217219099 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78261737 | CAAGACCTCCCGATG[A/G]CTTAGCCCCCATACC | 17972 |
rs217314481 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78257973 | TCTTCAGTGGTTCCC[A/G]TCAGGGACAAGGGAG | 17972 |
rs217378225 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78250338 | CTGGCTGTGTCCAGA[A/G]CAGGCAAGGTGGTAA | 17972 |
rs217394792 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78260925 | TTCTGGCACCACACA[C/T]GTCCCTCTTCCACCC | 17972 |
rs217441806 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78254925 | AAAATGTAGGTGGCC[A/G]TCCCTGCACTTCTGA | 17972 |
rs217442795 | snp | A/G | | | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262839 | TGGGGTACAAATCCC[A/G]CCCCAGCCACTTTGC | 17972 |
rs217695847 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78259099 | AGAAACCAGTCAGTA[C/G]GGATGAGTCCCAGGT | 17972 |
rs218080791 | in-del | -/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78247327 | ACGTCCCCACCCCCA[-/C]CCCCACCAACTGTCT | 17972 |
rs218359173 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78250647 | CAGTACACTGCAGGG[C/T]TTGAGAAAGCCTGTC | 17972 |
rs218360975 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78259263 | TGGCGTTCCCCTATA[C/T]TGAGTCATATAAAGT | 17972 |
rs218379584 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78256242 | GTGATGAGAATGGAG[A/G]TGAAGGTGGCAATGA | 17972 |
rs218417055 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78251512 | ATCTCCCATGCCACC[C/T]CCTCCCGAGCTTGCC | 17972 |
rs218468098 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78251985 | TTCCTGAGTCCCGTC[C/T]ACCTTTCTTGCTGCA | 17972 |
rs218486492 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78251905 | AGCCTCTGTTCTGAG[C/T]CTCCTATCCTGAGGG | 17972 |
rs218534867 | in-del | -/CCCCAC | | | intron-variant | Ncf4 | Mm_Celera | 15:78247315 | TGGCAATCCTAACGT[-/CCCCAC]CCCCACCCCCACCCC | 17972 |
rs218651613 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252998 | ATGAGTGTGTGTGTA[C/T]CTGTACACACCTTTG | 17972 |
rs218652206 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78258434 | CACTGGCAGACCTCA[A/G]GCTGCAGGAAGGGCC | 17972 |
rs218772085 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78253525 | GCAGACGGGATCAAG[A/G]AGCTGGGTCACAAAA | 17972 |
rs218987432 | snp | A/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242333 | TGTCTGTGTCTGCAT[A/G]TGCATGTATGTGTGT | 17972 |
rs219028389 | in-del | -/AC | | | intron-variant | Ncf4 | Mm_Celera | 15:78261237 | AAGCCTTGTACTTGG[-/AC]ACACACACACACACA | 17972 |
rs219033846 | snp | A/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78260395 | ATTAATTAATTAATT[A/T]AAAAAGAGGAAAGGA | 17972 |
rs219137736 | in-del | -/AAA | | | intron-variant | Ncf4 | Mm_Celera | 15:78249273 | ACTTGAATGGCCAGG[-/AAA]AAAAAAAAAACAACA | 17972 |
rs219417277 | in-del | -/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78245501 | GCCTCTGCGTTTTCC[-/T]ATCTTTAGGTTCAGA | 17972 |
rs219419696 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78255187 | GGCAGGGTCTGAATT[C/T]CGGCTTTGCAGGAGA | 17972 |
rs219473554 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78247824 | GGTGAGGCCACTCTT[C/T]CAGAGGATGTCCTCA | 17972 |
rs219706336 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78254422 | GATATGAGCACCTCC[A/G]GTGTCTCTGGATGCC | 17972 |
rs219777124 | in-del | -/TCTTCTGGAAGTAATGC | | | intron-variant | Ncf4 | Mm_Celera | 15:78261808 | TATACCGTCTCATTA[-/TCTTCTGGAAGTAATGC]TCAAGAAGTGGGATT | 17972 |
rs220102607 | in-del | -/TA | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242352 | ATGTATGTGTGTGTG[-/TA]TATTCGTGTCTGTGC | 17972 |
rs220161027 | snp | C/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242606 | TGGGATTACATGTGT[C/T]CTTACCCTTGTTTTA | 17972 |
rs220259717 | in-del | -/CTGCTCTC | | | intron-variant | Ncf4 | Mm_Celera | 15:78252004 | TTCTTGCTGCAGGCT[-/CTGCTCTC]CTGCTCACCTTGGGA | 17972 |
rs220334752 | in-del | -/C | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78244066 | CCCTACAGAACCAAG[-/C]ATTAGAAGGAGCTGA | 17972 |
rs220433676 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78252079 | ACAACTGGTGCCTGT[A/G]ACTTTGTCTCGTCTT | 17972 |
rs220491361 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78245398 | CCTGGGAGCAGAGGT[A/G]TCCTGGGTGCTAGGC | 17972 |
rs220545324 | snp | A/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243410 | CTTGAGCAGGGATTT[A/G]TATGCTTAAAAGAGC | 17972 |
rs220551674 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78245909 | TCAAGCAGAAAGCAA[A/C]GTTAGGAAGCCAAGT | 17972 |
rs220637416 | snp | C/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243639 | TGCCCTGCCTGGCCA[C/T]GGGGAGGGCAGTTCT | 17972 |
rs220740573 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78251794 | TTTCCCTGAGCTCTA[A/G]TCATTTTCCTTGACA | 17972 |
rs221037052 | in-del | -/CTCTC | | | intron-variant | Ncf4 | Mm_Celera | 15:78248367 | CTCCTCCTCCTCTTT[-/CTCTC]CTCCTCCTCTTCCTC | 17972 |
rs221108121 | in-del | -/CC | | | intron-variant | Ncf4 | Mm_Celera | 15:78251757 | CACCACTCTCCATCT[-/CC]CCCCCCCCTTTCCTA | 17972 |
rs221553112 | snp | C/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242521 | GCATACCTGCCCACA[C/T]ACAGTTGTACTCGTC | 17972 |
rs221689653 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78247981 | CCATCCTGGGACAGA[C/T]CAGGTCCCAGGGGAC | 17972 |
rs221929371 | snp | G/T | | | synonymous-codon | Ncf4 | Mm_Celera | 15:78261029 | CAAAGACCTGCTAGC[G/T]CTCATGAGGTGAGAG | 17972 |
rs222002421 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78246191 | TGACAGACATGCAAA[C/G]TTGAATCTTCTAGAA | 17972 |
rs222179214 | snp | G/T | | | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262995 | GCCAGGCAGTTGTGG[G/T]TGATAGCCTGAATCC | 17972 |
rs222642271 | snp | A/G | | | missense, downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262228 | AAGACATTGCCCTTA[A/G]CTACCAGGATGCTGA | 17972 |
rs222747819 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78261707 | CAATGTCCCCCTGGC[A/C]ATATCTACCATTCTC | 17972 |
rs222814903 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78254084 | TGCTCCATGTCCTCA[C/T]GCCTTAGTCACACTG | 17972 |
rs222881185 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78261726 | TCTACCATTCTCAAG[A/G]CCTCCCGATGACTTA | 17972 |
rs222888751 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78257482 | CTGCCATTCTCTTTA[A/G]TTTCTTGATCACTAA | 17972 |
rs222934772 | snp | C/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243799 | TTCTTGGAGCCAGAT[C/T]CTGAGGAGTCTGAGA | 17972 |
rs223001709 | snp | A/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78244160 | AAGCCTAACACACAA[A/G]CACACGTTTGGAACA | 17972 |
rs223103887 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78261340 | CTCACGATTCAAAAC[A/G]GCGCAGTCTGTATGA | 17972 |
rs223339216 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78259887 | TTTCCCCTTTACACG[C/T]GTAGCCATTGACCAC | 17972 |
rs223399154 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78260344 | GAGTAAAATTCTTGC[A/G]TTGTGGTTAGAAAGA | 17972 |
rs223737122 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78258238 | TCCCGGTATCCTGAG[A/G]CTGGGCAGGAGTGGG | 17972 |
rs223907315 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78261944 | GTTGTCACTGGTTCC[C/T]ACAGGCCTCCTGGGC | 17972 |
rs223966264 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78254599 | TCCCCTCCCCACTAC[C/T]CGCTCACGCTGGGCC | 17972 |
rs224103948 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78259291 | AGTTTACACGACCAA[G/T]GGGCCTCTCTTTCCA | 17972 |
rs224196493 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78259791 | GAGGCCCAAGCCTCC[A/G]GGTGACACCCAAAAC | 17972 |
rs224206012 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78257173 | GTTAGAAGAAAGGTA[G/T]TTTTGAGTGTTTTAC | 17972 |
rs224215014 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78261498 | ATACACACCCAAAAC[A/G]TATAACAAATGAGCA | 17972 |
rs224273028 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78260478 | TTTCTATTAGTATCT[A/G]TTTCTCCAAGCTCCC | 17972 |
rs224280074 | snp | A/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78257716 | TTCTCCACTGAGAGA[A/T]GTGAAGGCTCATATG | 17972 |
rs224328712 | snp | A/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78261109 | GTGACAGCTCCAGTC[A/T]CTGCAGTACACGGTG | 17972 |
rs224351283 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78250151 | GGGCACCAGGACCTG[A/G]CAAGTTCTTGGGTAG | 17972 |
rs224382839 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78253223 | AGGAGCATTGGGGAG[A/G]AGCACTGATTGGTGG | 17972 |
rs224526179 | in-del | -/TCAGATGGCCT | | | intron-variant | Ncf4 | Mm_Celera | 15:78246081 | AGTGTTGGGTGGGGG[-/TCAGATGGCCT]TCCTTCCATAGCTAT | 17972 |
rs225008225 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78253868 | CCCGGCTCTCAGCTC[C/T]CAATGAGTGGAGCTG | 17972 |
rs225036933 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78259598 | TATGCATTCGCACAC[A/G]TAAGTGCATGTATGT | 17972 |
rs225096397 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78259992 | CCCGGACCCATAGAT[C/T]GGGCATAGTGGTGCT | 17972 |
rs225096608 | snp | A/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78251868 | CCTGTCTGATGAGCG[A/T]TAACCAAGCAGCGCT | 17972 |
rs225155719 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78252226 | TGCCAAAGGCTCCTG[A/G]CGGACCTTCATCATT | 17972 |
rs225264687 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78249173 | TGAGCCTCAAGGGCA[A/G]GTGGGAATAGGAATA | 17972 |
rs225282902 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78255257 | TAAGGGCGCTGAGCC[A/G]TGATCCCCATTCCTT | 17972 |
rs225349145 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78247372 | GGTGTCTTGAAGAAC[A/G]TGATGAGGGTCACCC | 17972 |
rs225355960 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78258952 | GCTGGGCCCCCCACA[C/T]CAATCGTTAATAATA | 17972 |
rs225417024 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78257567 | ATAATTCCTGGGAAA[A/G]GGCAGGCTATTTAGG | 17972 |
rs225585758 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252948 | TAGAGTGTGTGTGTG[C/T]TGTGATGAGCATGTA | 17972 |
rs225648671 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78253455 | CATTTCCCTGAGGCC[C/T]CCACGATCCCATCTT | 17972 |
rs225662051 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78256142 | GGAGGTGAGGGTGGA[A/G]GTCAGATGGAGATGA | 17972 |
rs225714804 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78246886 | AGGGGTGGGAGGAGC[C/T]GGAGGATGGGGAGAG | 17972 |
rs225922557 | in-del | -/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78258051 | TCCCACTGCATGTGA[-/G]GGGGACTGGGAAGTC | 17972 |
rs226038074 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78251467 | CCCACCCCTGTCCCC[C/T]ATCTCCTTCCCATAT | 17972 |
rs226233085 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78255574 | TGCTGTGTGCCACTG[C/T]GCACTTTGGATGGTG | 17972 |
rs226303554 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78248462 | TGCAGCCTGGGCTGA[C/G]CTAGAACTCCTCATT | 17972 |
rs226683530 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78252604 | TGTGTGCATTTGTGT[A/G]TATACATATACATAT | 17972 |
rs226712933 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78250316 | GGGGTGTGCAGGCCT[C/T]CATCAGCTGGCTGTG | 17972 |
rs227133470 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78245483 | CCCTTCAGACTGAAA[C/T]TGGCCTCTGCGTTTT | 17972 |
rs227191397 | in-del | -/GA | | | upstream-variant-2KB, intron-variant | Ncf4 | GRCm38.p3 | 15:78244450 | GAGGCAGATTGTAAG[-/GA]GAGAGCCTCTGTGTG | 17972 |
rs227230012 | snp | A/G | | | synonymous-codon | Ncf4 | Mm_Celera | 15:78253346 | TGAGACTCGGATCCC[A/G]GCCCTCAATGCCTAC | 17972 |
rs227535860 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78246232 | CTAGAAGCTTGGGTC[A/C]CTTCTTGTTTCTTGG | 17972 |
rs227767002 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78247795 | CTGCCCCACCCCAGC[C/T]TCTGGGGGAAGTGGG | 17972 |
rs227806137 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78247001 | GTCTTCTGACACTAG[C/T]GCTGCCCAGACACTT | 17972 |
rs227855630 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78247477 | ATGGAGTACAAGAAG[A/C]AGAGAGCAGGACCCC | 17972 |
rs228010206 | in-del | -/AC | | | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78263023 | CCCAGAGCTGCCATG[-/AC]AGAGTACCACAAAAT | 17972 |
rs228237801 | snp | A/G | | | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262778 | CAGAGTTTGGGAACT[A/G]TTGGGTCTATGGTAT | 17972 |
rs228588975 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78248044 | GTGGGCTCCTGGGGA[C/T]CCCATACTTTGTGAG | 17972 |
rs228617139 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78258782 | TTATAACGTTTCCAT[C/T]CCTGAGCGAAGTCAG | 17972 |
rs228679764 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78259526 | TGTACACATACACAG[A/G]CACATGTATGTACAC | 17972 |
rs228825511 | snp | C/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243154 | CCTCGGGCACCCAGG[C/T]CAATGGCTGAGAAAC | 17972 |
rs228852823 | in-del | -/TA | | | intron-variant | Ncf4 | Mm_Celera | 15:78252640 | GTATATGTATGTATG[-/TA]TATATATATATGCAT | 17972 |
rs228908304 | in-del | -/A | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78245353 | GGCTTGGATGTGGCC[-/A]AAGGACCACAGGGTG | 17972 |
rs228927041 | in-del | -/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252694 | GGCCTTACATGTGTA[-/T]TTGCATATATGTGTA | 17972 |
rs229100915 | snp | A/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243987 | ATACCATCAAGTGGA[A/G]CTGGGGGTTGGGGGA | 17972 |
rs229152310 | in-del | -/A | | | intron-variant | Ncf4 | Mm_Celera | 15:78249274 | ACTTGAATGGCCAGG[-/A]AAAAAAAAACAACAA | 17972 |
rs229315294 | in-del | -/A | | | intron-variant | Ncf4 | Mm_Celera | 15:78245708 | CTCACTACATCTGCT[-/A]AGAGCTCAAAAATGA | 17972 |
rs229467330 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78260149 | AACTAGAGTGCAGGT[C/T]TCTGGGTTAGGCAGC | 17972 |
rs229626704 | snp | C/T | | | synonymous-codon | Ncf4 | Mm_Celera | 15:78260689 | CCTTAAGGACTTTCC[C/T]GAGGACGAGGACACC | 17972 |
rs229808161 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78260350 | AATTCTTGCATTGTG[A/G]TTAGAAAGAAAAATA | 17972 |
rs229847588 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78260931 | CACCACACACGTCCC[C/T]CTTCCACCCTGATGC | 17972 |
rs229885475 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78252999 | TGAGTGTGTGTGTAC[C/G]TGTACACACCTTTGT | 17972 |
rs230062750 | snp | A/G | | | intron-variant, missense | Ncf4 | Mm_Celera | 15:78262168 | GAGAAGCCAGGATCC[A/G]TAGACTAATCCTGGT | 17972 |
rs230118344 | snp | A/C | | | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262844 | TACAAATCCCGCCCC[A/C]GCCACTTTGCTTTGG | 17972 |
rs230118489 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78255107 | CGTTCGAGCCACTTC[C/T]TTAAGAAGCCAAGGA | 17972 |
rs230174610 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78255827 | TGTATCAGCACCCTT[C/T]CAAACCCTCAGTTTC | 17972 |
rs230525822 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78261417 | GTCAGCACATGCACA[A/C]ACATGTGTAGGCACA | 17972 |
rs230660922 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78251221 | TGCTACAGTTTCTGC[A/G]TCATAACCCTTGACC | 17972 |
rs230664222 | in-del | -/AGCATTGGGGAGA | | | intron-variant | Ncf4 | Mm_Celera | 15:78253211 | TCTGGGCTGGGGAGG[-/AGCATTGGGGAGA]AGCACTGATTGGTGG | 17972 |
rs230838079 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78262008 | TCCACCCACTTATAC[A/G]CAAGAAGCTTCAGGC | 17972 |
rs230992189 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78257458 | TTTCACAGCCTCCTC[C/T]CCCCACCCCTGCCAT | 17972 |
rs231075307 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78258095 | TGAAGCTGGGCCCCC[C/T]TGGGTGTTTCTTTGC | 17972 |
rs231185173 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78251986 | TCCTGAGTCCCGTCC[A/G]CCTTTCTTGCTGCAG | 17972 |
rs231242767 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252533 | GTCCTGAGTTCAGAG[C/T]GTGCATCTGTTTTAT | 17972 |
rs231410511 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78257892 | ATGCATTTCTAGCTG[G/T]CCTTGTGTACCTCAG | 17972 |
rs231524182 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78258662 | GGACTTGCTGTCCAG[C/T]CGCAAACCAGCTACA | 17972 |
rs231706136 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252264 | TCATGCACTCCGCTC[C/T]GCGTTAGAGGCATGG | 17972 |
rs231729307 | in-del | -/TGTGTGCAT | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242183 | GTGTGTGTTTGTGTG[-/TGTGTGCAT]TGTGTGCATGTGTGT | 17972 |
rs232013111 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78260033 | TGCTGAAGGAAAGAA[C/T]GGATGAGGAAGAGAA | 17972 |
rs232136946 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78261467 | ACACACACAAAAAAA[A/C]CAAACACACGAACCA | 17972 |
rs232165968 | in-del | -/AA | | | intron-variant | Ncf4 | Mm_Celera | 15:78259476 | TGTAGATAAAGACTG[-/AA]GAGTGACATCTGAAG | 17972 |
rs232189400 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78253501 | TGGCTGGAGAGAGAA[A/G]CAAGGTATGCAGACG | 17972 |
rs232248319 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78248938 | GCATTAGACTGCAGG[A/G]AAAGGCTGGTCTGGT | 17972 |
rs232284912 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78252861 | CATGCATATGAGTGT[A/G]TATTCATGTGTCTAT | 17972 |
rs232526988 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78259626 | TGTACTTACACACAT[A/G]CAAATACATAAGTAT | 17972 |
rs232634060 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78253117 | CACTTGGTACCATGA[C/T]AGAAGGCAGGAGGAA | 17972 |
rs232724423 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78253777 | TTTGTTTGGATGGGT[G/T]CTTTGGAGCGAGTAA | 17972 |
rs232829261 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78254755 | CTGTCTAGATCTTTC[C/T]GTCGACTGCCCACCT | 17972 |
rs232836619 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78261770 | GGTTACCACTGACAA[C/G]AATATTGTAAATCTT | 17972 |
rs232861457 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78249999 | CATGAGGCTCCCTAC[C/G]TAGAGGTCCACAACA | 17972 |
rs233054243 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78255623 | ATGCCATGGCAAAGA[A/G]CAGTGGGATGGATGC | 17972 |
rs233203870 | in-del | -/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78253185 | CTGGGGAGGAGCACT[-/G]GGGGAGGAGCTCTGG | 17972 |
rs233236111 | in-del | -/CTC | | | intron-variant | Ncf4 | Mm_Celera | 15:78248120 | CAATCACTTCTTCAA[-/CTC]CTCCTCCTCCTCACC | 17972 |
rs233334364 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78245928 | AGGAAGCCAAGTGTC[C/T]ATGTGAACTGCTTGA | 17972 |
rs233349628 | in-del | -/ACACACAC | | | intron-variant | Ncf4 | Mm_Celera | 15:78261236 | AAGCCTTGTACTTGG[-/ACACACAC]ACACACACACACACA | 17972 |
rs233416500 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78254513 | TTACAGGTTTCTGGT[A/G]TAATCAGCCTCCTTA | 17972 |
rs233659514 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78249441 | CTCTCCCCCTCCTTC[A/G]TGGCTGGCCACCTGT | 17972 |
rs233698558 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78261635 | GAAACACAAATATAC[A/G]TAAATACCTAAAACA | 17972 |
rs233721835 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78251834 | CCTCTGGAGCATGTG[A/C]AGAGGTCCCCCATCA | 17972 |
rs233757881 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78262044 | CATTATTGGATTACC[C/G]AGTGTCCTCTTCCTT | 17972 |
rs233779987 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ncf4 | Mm_Celera | 15:78244396 | TTCTGAAGCCAGCAG[C/T]GGGGGCTTGGGGCTT | 17972 |
rs234071679 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78257104 | TGGGGTTGAAGTTAG[A/G]GATGAGGATGGAGGT | 17972 |
rs234244899 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252902 | GTGTATGTGCATAGG[C/T]TTATGCATGTCTAAG | 17972 |
rs234310666 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78250839 | CGTTCTAGCTCCCCT[C/T]CCCCAGTCTCTCTCC | 17972 |
rs234315596 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78246633 | CGTGTGCACGGAGCC[C/T]GGTATCCACCCAACA | 17972 |
rs234318691 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78251433 | TTGGGGAAGCAGGGA[C/G]CCACACATAGCTTCT | 17972 |
rs234327797 | in-del | -/CTGCAA | | | intron-variant | Ncf4 | Mm_Celera | 15:78259402 | AGGGGCTAAAGGGAT[-/CTGCAA]CCCTATAGGTGGAAC | 17972 |
rs234488742 | snp | C/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242580 | TCCTCCTGCCTCCAC[C/G]TCCTGAGAACTGGGA | 17972 |
rs234665578 | in-del | -/TCTATTTGTG | | | intron-variant | Ncf4 | Mm_Celera | 15:78252824 | ATAAGTTCTTGTGTA[-/TCTATTTGTG]TGCATTTGTGTGCAT | 17972 |
rs234879754 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78247769 | GCTATTTTTCCCTTT[C/G]CAGTTCCCTCCTGCC | 17972 |
rs234918233 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78259169 | TATTTTATTTATTTA[C/T]ATTTCCAGTGCTATC | 17972 |
rs234985329 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78259668 | CACACATATAAATAT[A/G]GATACCAAAAAGAAT | 17972 |
rs235093371 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78246768 | ACAAGTGGAAGTAGC[C/T]GCTCAGGACCTTCTA | 17972 |
rs235928198 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78247058 | TTGCTGTTCTTCCAC[A/G]AGGCAGGAAGGCCCC | 17972 |
rs235946545 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78254233 | TCCTTATGATTCATT[G/T]GATAGAGTGCTTGCC | 17972 |
rs236230224 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78261343 | ACGATTCAAAACAGC[A/G]CAGTCTGTATGAGGA | 17972 |
rs236294454 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78261710 | TGTCCCCCTGGCCAT[A/G]TCTACCATTCTCAAG | 17972 |
rs236396751 | in-del | -/GAGGTTG | | | intron-variant | Ncf4 | Mm_Celera | 15:78261041 | GCGCTCATGAGGTGA[-/GAGGTTG]GAGGTTGGGAAGGGA | 17972 |
rs236401578 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78261062 | TGGGAAGGGAGGGAG[A/C]CTTTGGAGGGCAATG | 17972 |
rs236862983 | in-del | -/GCTCTGACCCTGTGCATTA | | | upstream-variant-2KB | Ncf4 | GRCm38.p3 | 15:78243097 | GGCTTCAGGCTCGAG[-/GCTCTGACCCTGTGCATTA]GCTCCCTCTGTCTAC | 17972 |
rs237130823 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78257335 | CATTCATGCCACAGC[A/G]TATGTGAGGGAACAG | 17972 |
rs237178978 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78251657 | AAACACATTCTCTTC[A/C]TCCATCTCCAAAAAG | 17972 |
rs237368581 | snp | A/G | | | synonymous-codon, downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262259 | GGGGGACTTGGTTAG[A/G]CTGCTGTCAGATGAG | 17972 |
rs237513587 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78258611 | CTTGTGCTTATCATC[C/T]AGCTCTGGGGGAGAC | 17972 |
rs237589976 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78250721 | GTCTCTACCTCCCAG[C/G]CCCTCCCCAGCCCCC | 17972 |
rs237592167 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78259268 | TTCCCCTATATTGAG[G/T]CATATAAAGTTTACA | 17972 |
rs237728209 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78260225 | TCACTATAATAGAAC[A/G]CCCGAGGCATCTAGC | 17972 |
rs237875413 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78256330 | TGATGATGGGGTAAG[A/G]GTGGGGGATGGTGGT | 17972 |
rs238027723 | in-del | -/AGG | | | intron-variant | Ncf4 | Mm_Celera | 15:78254330 | ATAATCCCAACACTT[-/AGG]AGGTAGAGGCAAGAT | 17972 |
rs238150089 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78259061 | TCCCTCTTTCTAGAC[A/G]ACTCTCTTTGTGTCA | 17972 |
rs238345709 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78249309 | AACAAAACACCAAAA[C/T]AGCAGGAACATATGG | 17972 |
rs238350475 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252563 | TGCAAGTGTACGTAT[G/T]TTTGTGTGTTAAAGC | 17972 |
rs238405665 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78249844 | AAAGCACGGCAACCC[C/T]TTTGCCTGAGTCTCT | 17972 |
rs238573474 | in-del | -/A | | | intron-variant | Ncf4 | Mm_Celera | 15:78254295 | AGTATCAAATAAAAT[-/A]GACATGGTGGCCCAC | 17972 |
rs238688153 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78260323 | CATCCTGACAGGAGC[A/G]TGTGAGAGTAAAATT | 17972 |
rs238796963 | in-del | -/GTGTG | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78246054 | AGAGGAGGTTTGTCT[-/GTGTG]GTAACAAGAGTTAGT | 17972 |
rs238914338 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78261556 | CACAAACACACAAAG[A/C]TATAACACACAAACA | 17972 |
rs239046471 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78252228 | CCAAAGGCTCCTGGC[A/G]GACCTTCATCATTTG | 17972 |
rs239062080 | in-del | -/AGCCACTAGA | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78246212 | TCTTCTAGAAACTGT[-/AGCCACTAGA]AGCTTGGGTCCCTTC | 17972 |
rs239065543 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78256119 | GATGATGGGGTGGAA[C/G]TGGAATTGGAGGTGA | 17972 |
rs239111965 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252848 | GTGCATTTGTGTGCA[C/T]GCATATGAGTGTGTA | 17972 |
rs239556934 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78257993 | GGACAAGGGAGAGGC[A/G]GATGTCCTCCAGGCC | 17972 |
rs239581252 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78246198 | CATGCAAACTTGAAT[C/T]TTCTAGAAACTGTAG | 17972 |
rs239693758 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78245438 | GGGTTCCTGGTTCCA[C/T]ACTGCAATCAGGAGC | 17972 |
rs239736427 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78258243 | GTATCCTGAGGCTGG[A/G]CAGGAGTGGGAGTGG | 17972 |
rs240096798 | in-del | -/GACACACACACACACA | | | intron-variant | Ncf4 | Mm_Celera | 15:78261236 | AAAGCCTTGTACTTG[-/GACACACACACACACA]CACACACACACACAC | 17972 |
rs240463069 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78251881 | CGTTAACCAAGCAGC[C/G]CTGTGGGGAGCCTCT | 17972 |
rs240572342 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78260870 | CTGCAGCTGCTGCTG[C/T]GGCTCCCAGATAAAC | 17972 |
rs240587712 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78251980 | CAGCCTTCCTGAGTC[C/G]CGTCCACCTTTCTTG | 17972 |
rs240784516 | snp | C/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242878 | CCACTGCACCCCTCC[C/T]TGCTCCCCTGGTTGT | 17972 |
rs240846120 | snp | A/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243647 | CTGGCCACGGGGAGG[A/G]CAGTTCTCACTGGGC | 17972 |
rs241019073 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252202 | TGGGTGGCAGCTCCT[C/T]TAAGTGTCTGCCAAA | 17972 |
rs241257475 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78258306 | CCTCCTTGTGCACTG[A/G]GTCTCAGAAGCCATG | 17972 |
rs241280701 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78246772 | GTGGAAGTAGCCGCT[C/G]AGGACCTTCTAGGCG | 17972 |
rs241441749 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78246734 | CTTGGCAGCTCAGCT[A/G]CAGACGGCTCACACT | 17972 |
rs241569690 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78257637 | TTCCCACTAGGTGTC[A/G]CCAGTGCACCTGGTC | 17972 |
rs241775655 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78261781 | ACAAGAATATTGTAA[A/C]TCTTCATTCACATAT | 17972 |
rs241896681 | snp | C/G | | | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78263075 | AACTGCCTTGTAGTT[C/G]TGGATGGCAGAAGTC | 17972 |
rs241921893 | snp | A/G | | | synonymous-codon | Ncf4 | Mm_Celera | 15:78254900 | CCGCAGGCTCCGACC[A/G]CGCACGCGCAAAATG | 17972 |
rs242172758 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78249823 | GGGTTCCATGGATCC[C/T]GCCTAAAAGCACGGC | 17972 |
rs242247140 | in-del | -/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78253843 | TATGAGACGAACAGT[-/C]CCCACCCTCCCCGGC | 17972 |
rs242580145 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78257375 | GTTGACCCTCTCCTG[C/T]CAGGCTGGTTGTGGA | 17972 |
rs242586844 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78252433 | GGGGAGCCCTATCTA[A/G]TGGGATGCTCAAAAG | 17972 |
rs242588481 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78260616 | CCAGCCTCTTCTTTC[A/G]CTTCCAGGGCACCTC | 17972 |
rs242641413 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252908 | GTGCATAGGCTTATG[C/T]ATGTCTAAGCTTTGC | 17972 |
rs242653502 | snp | A/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242666 | ACTCACGCTACACAA[A/G]TGCTCTGCATCCCAG | 17972 |
rs242813508 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ncf4 | Mm_Celera | 15:78244208 | CCGCTGGTGAGAGCT[C/T]GCCGCAGGAAAAGCC | 17972 |
rs242820380 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78251469 | CACCCCTGTCCCCCA[C/T]CTCCTTCCCATATGC | 17972 |
rs242910184 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78259559 | TCACATAAATGCACA[C/T]ACATGCTCACATGCA | 17972 |
rs242971913 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78259950 | GCCATCAGGAGTGCT[G/T]CATGAGGGAACAGTG | 17972 |
rs243067346 | in-del | -/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78258823 | ACCTGGAGGCAGAAA[-/C]TGAAGCTGAGGCCAT | 17972 |
rs243207043 | in-del | -/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78253909 | AGAAAATTAAGGGAA[-/G]GGGGTTTTAGAACTG | 17972 |
rs243242438 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78260008 | GGGCATAGTGGTGCT[C/T]GAGAACCTCTGCTGA | 17972 |
rs243280783 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78257264 | GGAGGTCCTGGCAGG[G/T]TTGGGTGACCTGTGG | 17972 |
rs243521372 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78245765 | CATTATACAGGTAGG[A/G]ACAAGGAGACCTGAT | 17972 |
rs243712370 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78249605 | ACTACCCGGAAGAAC[C/T]TTCCTAGATTCCAGT | 17972 |
rs243777755 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78250193 | AGCCAGCTGGTGACA[A/C]CAATTCCAGCTCCGC | 17972 |
rs243930494 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252605 | GTGTGCATTTGTGTA[C/T]ATACATATACATATG | 17972 |
rs243981766 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78254624 | TGGGCCAGGAGCAAA[G/T]CTTGGGAATTGTCTC | 17972 |
rs244240051 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78261508 | AAAACATATAACAAA[C/T]GAGCACAAACACACA | 17972 |
rs244298889 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78253696 | CATCCAAGCCATGGT[C/G]TGCTGGAAAGCCTTC | 17972 |
rs244299034 | snp | A/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78261955 | TTCCTACAGGCCTCC[A/T]GGGCAGCCTTGCTTT | 17972 |
rs244406139 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78252953 | TGTGTGTGTGCTGTG[A/C]TGAGCATGTATGTGT | 17972 |
rs244667180 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78255222 | GGCTCTGAGAGCCAG[A/G]TTGAGGTCTGGTGGA | 17972 |
rs244806398 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78246516 | TTTAGCTCCCATGGC[C/T]ACATGTCATTCCAGC | 17972 |
rs244867373 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78246970 | GGGTATTATCTGGCC[C/T]TGTCTGGCCTAGTAT | 17972 |
rs244874024 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78257543 | GGTGGGGTGGGGTCG[G/T]GGAGACAGATAATTC | 17972 |
rs245074145 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78251879 | AGCGTTAACCAAGCA[G/T]CGCTGTGGGGAGCCT | 17972 |
rs245129387 | snp | A/G | | | utr-variant-5-prime, intron-variant | Ncf4 | Mm_Celera | 15:78244884 | GAAGGAGGTACTTCA[A/G]GGAGGGTCCAGAGAA | 17972 |
rs245323319 | in-del | -/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78246284 | CTGTAAGGACTATCA[-/G]GGCTCAGTGTTTCCT | 17972 |
rs245387237 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78251302 | GGAGCCTGGGCTGGG[A/C]GCACTCAGCACCTGG | 17972 |
rs245928729 | snp | A/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243977 | CTGTCTTAGCATACC[A/G]TCAAGTGGAGCTGGG | 17972 |
rs246135467 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78260453 | GCCCTCTCCCTAGCA[A/G]GAAAGGACATTTCTA | 17972 |
rs246260331 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78259348 | ATATATATTGGATGG[A/G]TCCCAGGGCCCCCAA | 17972 |
rs246345486 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78251813 | TTTTCCTTGACACAC[C/T]GCCCCCCTCTGGAGC | 17972 |
rs246517170 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252888 | CTATGTGAGTGAGGG[C/T]GTATGTGCATAGGCT | 17972 |
rs246829554 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78248311 | TCCTCCTCCTCCTCC[C/T]TTTCCTCCCCTTTCT | 17972 |
rs246900984 | snp | C/G | | | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262808 | TTACATCCACAGCTG[C/G]CCTGCCCCAGACCCA | 17972 |
rs246925954 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78260564 | ACAATCGTTGTTGTA[A/G]AGAGTGTGGGACTCT | 17972 |
rs247124114 | in-del | -/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78261083 | GAGGGCAATGCGCTA[-/G]GAGGGGACCTGTGAC | 17972 |
rs247418441 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78257079 | ATGGAGGTGAGGATA[G/T]AGGTGAAGATGGGGT | 17972 |
rs247656514 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78260887 | GCTCCCAGATAAACC[A/G]TAGTGCTTTAGCAAG | 17972 |
rs247710001 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78261491 | CGAACCAATACACAC[C/T]CAAAACATATAACAA | 17972 |
rs247890524 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78259180 | TTTACATTTCCAGTG[A/C]TATCCCAAAAGTCCC | 17972 |
rs247898712 | snp | A/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78256167 | AGATGAGATTGGAGG[A/T]AGGGCTGAGGTGGAG | 17972 |
rs247989388 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78249189 | GTGGGAATAGGAATA[A/G]GAGCAATGTTTGGTC | 17972 |
rs248099833 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78250585 | TTCAGCGGTGCTTCT[A/G]AACACATCCAAAAGC | 17972 |
rs248866813 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78259839 | GCACTTTCAGGTCTC[C/T]CTGCAGTCCCCAATG | 17972 |
rs248898206 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78258795 | ATCCCTGAGCGAAGT[C/G]AGGACAAGAAATAAC | 17972 |
rs248964859 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78252090 | CTGTGACTTTGTCTC[A/G]TCTTGGTGTGTGGCT | 17972 |
rs248999307 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78255145 | GCAGGAATCTTGAGC[C/T]CTGACCTCCGCCAAA | 17972 |
rs249207277 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78261329 | CTGTCCCATCTCTCA[C/T]GATTCAAAACAGCGC | 17972 |
rs249232822 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78258061 | ATGTGAGGGGACTGG[A/G]AAGTCTTGAATGTGA | 17972 |
rs249291578 | snp | C/T | | | synonymous-codon | Ncf4 | Mm_Celera | 15:78253313 | CAAAGTCTACATGGG[C/T]GCAAAACAAGAGATC | 17972 |
rs250189527 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78252033 | GATGGGACTCTCCCC[A/C]ATCCTTGCCTGTCTC | 17972 |
rs250250990 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78252553 | ATCTGTTTTATGCAA[A/G]TGTACGTATTTTTGT | 17972 |
rs250261710 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78260367 | TAGAAAGAAAAATAA[A/G]TAAGTAAAATAGATT | 17972 |
rs250324048 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78252714 | ATATATGTGTATGTC[A/G]GTATACTATATGTGT | 17972 |
rs250326044 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78260947 | CTTCCACCCTGATGC[G/T]TGTCTCTTCTACTGT | 17972 |
rs250397006 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78253057 | CTCCTTCTGCCTTCT[C/T]CTGATGGTATGATGG | 17972 |
rs250504391 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78255317 | GGAGAGCAACCTCAC[C/T]TGGGGCAGTGGTGAG | 17972 |
rs250504398 | in-del | -/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243743 | GGGTGACAGGATGGA[-/G]GGGGGGACATTTTAA | 17972 |
rs250581720 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78248030 | TCTGTGCAGGGTGTG[C/T]GGGCTCCTGGGGATC | 17972 |
rs250767192 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78250023 | CACAACACTCCCCAG[G/T]GGTGATGTCCATTAA | 17972 |
rs251180231 | in-del | -/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242192 | GTGTGTGTGTGCATT[-/G]GTGTGCATGTGTGTG | 17972 |
rs251207313 | snp | A/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78260272 | TTTGCTATGGCTCAC[A/T]ATGCTGGAAGCTCCA | 17972 |
rs251313180 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78249131 | CCAACTCCATCTCAT[G/T]GACCAGAGCTAGTCA | 17972 |
rs251373334 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78249740 | CTCTCTGTCTGTCAG[C/T]CTCATGGTACTATGA | 17972 |
rs251395199 | snp | A/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242281 | TGTGTATCTGTGACT[A/G]TATGTGCGTGTCTCT | 17972 |
rs251425707 | snp | C/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242515 | AAACAGGCATACCTG[C/T]CCACACACAGTTGTA | 17972 |
rs251426695 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78257459 | TTCACAGCCTCCTCC[C/T]CCCACCCCTGCCATT | 17972 |
rs251486095 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78258232 | CAGGGTTCCCGGTAT[C/T]CTGAGGCTGGGCAGG | 17972 |
rs251998049 | in-del | -/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78257543 | GGTGGGGTGGGGTCG[-/T]GGAGACAGATAATTC | 17972 |
rs252083719 | in-del | -/TCAGGTCACAG | | | intron-variant | Ncf4 | Mm_Celera | 15:78258776 | TTAAGTTATAACGTT[-/TCAGGTCACAG]TCCATCCCTGAGCGA | 17972 |
rs252175433 | in-del | -/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78254664 | TGAGGACTAGTAACG[-/T]TTTTTGTTTTTGTTT | 17972 |
rs252289484 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78255577 | TGTGTGCCACTGTGC[A/C]CTTTGGATGGTGTTG | 17972 |
rs252326201 | in-del | -/TCT | | | intron-variant | Ncf4 | Mm_Celera | 15:78258065 | GAGGGGACTGGGAAG[-/TCT]TGAATGTGACCCTGA | 17972 |
rs252632183 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78253132 | TAGAAGGCAGGAGGA[A/G]CCCTGAGCTGGGGAG | 17972 |
rs252696846 | snp | A/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78261681 | AAGAAGCACACACAC[A/T]CACTCACTCACAATG | 17972 |
rs252741655 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78262049 | TTGGATTACCCAGTG[C/T]CCTCTTCCTTTGAGG | 17972 |
rs252783293 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78247181 | ATTGTCCCTCTTATA[C/T]GATTTCCAGGGAGTC | 17972 |
rs253231869 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Ncf4 | Mm_Celera | 15:78244167 | ACACACAAACACACG[C/T]TTGGAACACACTGGG | 17972 |
rs253439321 | snp | A/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78259629 | ACTTACACACATACA[A/T]ATACATAAGTATACA | 17972 |
rs253452658 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78246350 | CCCTCTGAGGGGGGT[A/G]GCTCTCCTCCTCTGC | 17972 |
rs253500762 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78251892 | CAGCGCTGTGGGGAG[A/C]CTCTGTTCTGAGCCT | 17972 |
rs253569787 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78258375 | AAGAGGAACTGTTGA[C/T]CGCTTTACTGTCTTC | 17972 |
rs253660396 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78257078 | GATGGAGGTGAGGAT[A/G]TAGGTGAAGATGGGG | 17972 |
rs253752459 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78254564 | AGGTGATTTCAGATG[A/C]CCTCTTAAGCCAGCA | 17972 |
rs253870139 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78257647 | GTGTCACCAGTGCAC[C/T]TGGTCACAGCAATCA | 17972 |
rs253873284 | snp | C/G | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243727 | GCCAGAAGATCCCTT[C/G]AGGGTGACAGGATGG | 17972 |
rs253926350 | snp | A/G/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78244147 | GCTGGCCTGGAAGAA[A/G/T]CCTAACACACAAACA | 17972 |
rs253987109 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78245292 | TTGACTTAGTAGGTC[A/G]GCAGTGTTATGCACC | 17972 |
rs254080672 | in-del | -/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78258943 | ATACAGTGGGCTGGG[-/C]CCCCCACATCAATCG | 17972 |
rs254325159 | snp | G/T | | | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262850 | TCCCGCCCCAGCCAC[G/T]TTGCTTTGGGTAGGT | 17972 |
rs254382071 | in-del | -/CCC | | | intron-variant | Ncf4 | Mm_Celera | 15:78251756 | CACCACTCTCCATCT[-/CCC]CCCCCCCCCCTTTCC | 17972 |
rs254654833 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78254269 | TTTGAGAAGTCCTGG[A/G]TTTGTTCCCCAGTAT | 17972 |
rs254667210 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78257106 | GGGTTGAAGTTAGGG[A/G]TGAGGATGGAGGTGA | 17972 |
rs254726304 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78249528 | CCACCTTAAGACCCA[C/G]CAGGCTCTCAGCAAA | 17972 |
rs254835746 | snp | A/C | | | synonymous-codon | Ncf4 | Mm_Celera | 15:78260629 | TCACTTCCAGGGCAC[A/C]TCCCAGGGAGCCACA | 17972 |
rs254898054 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78261369 | GAGGACTATATTGCA[C/T]TCCTATCGTTAGCTG | 17972 |
rs254960697 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78253447 | AAAACTGACATTTCC[C/T]TGAGGCCTCCACGAT | 17972 |
rs255166959 | in-del | -/TTA | | | intron-variant | Ncf4 | Mm_Celera | 15:78259136 | AGACCCTGTTTCTTT[-/TTA]TTATTATTATTATTA | 17972 |
rs255197666 | snp | G/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242329 | TGTGTGTCTGTGTCT[G/T]CATGTGCATGTATGT | 17972 |
rs255265943 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78251489 | TTCCCATATGCCCCT[C/T]GTCCCAAATCTCCCA | 17972 |
rs255485246 | snp | C/G | | | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78263044 | ACCACAAAATGGAGA[C/G]TAAAAGACAGAAAGA | 17972 |
rs255545986 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78256168 | GATGAGATTGGAGGA[A/C]GGGCTGAGGTGGAGG | 17972 |
rs255607379 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78257417 | GGTTGTCAGACATGG[C/T]AGCACCCTCTTTATC | 17972 |
rs255790604 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78259608 | CACACATAAGTGCAT[A/G]TATGTACTTACACAC | 17972 |
rs255877026 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78251756 | ACACCACTCTCCATC[C/T]CCCCCCCCCCTTTCC | 17972 |
rs255956809 | snp | G/T | | | upstream-variant-2KB, intron-variant | Ncf4 | Mm_Celera | 15:78244212 | TGGTGAGAGCTTGCC[G/T]CAGGAAAAGCCCGGA | 17972 |
rs255977103 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78260858 | CTCTCCCCTCCCCTG[A/C]AGCTGCTGCTGTGGC | 17972 |
rs256130427 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78259592 | TCTGCATATGCATTC[A/G]CACACATAAGTGCAT | 17972 |
rs256185059 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78259958 | GAGTGCTGCATGAGG[C/G]AACAGTGCTTGTGTA | 17972 |
rs256265844 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78250776 | GTCCACCTCTCAGCT[A/C]TCCTACCTTATAAAG | 17972 |
rs256619774 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252213 | TCCTTTAAGTGTCTG[C/T]CAAAGGCTCCTGGCG | 17972 |
rs257200105 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78254756 | TGTCTAGATCTTTCC[A/G]TCGACTGCCCACCTG | 17972 |
rs257229127 | in-del | -/CTC | | | intron-variant | Ncf4 | Mm_Celera | 15:78248278 | CATTGGAATTCTATT[-/CTC]CTCTTCCTCCTCTCT | 17972 |
rs257255801 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78255413 | TCTCCCTGCATCTCC[A/G]GGGACCCACAAGGCT | 17972 |
rs257261020 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78247948 | GTCACTGCCTGGTGA[C/T]TTCTGAATCCAGATA | 17972 |
rs257316344 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78256388 | GATGGGGGTGAGGAT[A/G]GAGGTGAGGATGAGG | 17972 |
rs257316426 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78248180 | TCCCTTCTCCTTCCT[C/T]TATCTCGCCCTCCTT | 17972 |
rs257360698 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78257336 | ATTCATGCCACAGCA[C/T]ATGTGAGGGAACAGC | 17972 |
rs257485505 | snp | C/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243600 | GACTTTCTTCATCCT[C/T]GTTTCTGTCTCCCCA | 17972 |
rs257527808 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78258695 | TTGGCCAAGTTCCAG[C/T]TTGCTTTCTGTCCCT | 17972 |
rs257763738 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78249377 | TTGCATGTCCTGGCC[C/G]ATATCACCCTTCACT | 17972 |
rs257831279 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78259281 | AGTCATATAAAGTTT[A/G]CACGACCAATGGGCC | 17972 |
rs258112949 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78248120 | CCAATCACTTCTTCA[A/G]CTCCTCCTCCTCACC | 17972 |
rs258429902 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252259 | GACCTTCATGCACTC[C/T]GCTCCGCGTTAGAGG | 17972 |
rs258493190 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78245609 | GGGGCCGGGTCTTTG[C/T]TCTGCCTGCTCTGAG | 17972 |
rs258494495 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78252859 | TGCATGCATATGAGT[A/G]TGTATTCATGTGTCT | 17972 |
rs258502417 | in-del | -/CGG | | | intron-variant | Ncf4 | Mm_Celera | 15:78246632 | CGTGTGCACGGAGCC[-/CGG]TGGTATCCACCCAAC | 17972 |
rs258540734 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78253811 | GTCCTCTCTCAGGAA[C/G]TCTCAGCTTCCTTCT | 17972 |
rs258672465 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78256127 | GGTGGAAGTGGAATT[A/G]GAGGTGAGGGTGGAG | 17972 |
rs258702258 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78260125 | CAGATAAGTTCAGGG[A/C]TCTTATAAAACTAGA | 17972 |
rs258777309 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252266 | ATGCACTCCGCTCCG[C/T]GTTAGAGGCATGGCT | 17972 |
rs258927976 | snp | A/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78253514 | AAGCAAGGTATGCAG[A/T]CGGGATCAAGGAGCT | 17972 |
rs258963596 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ncf4 | Mm_Celera | 15:78244388 | CTTGGGGATTCTGAA[A/G]CCAGCAGCGGGGGCT | 17972 |
rs259001333 | snp | C/T | | | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262976 | TGGCCTGTGGAGATG[C/T]AAGGCCAGGCAGTTG | 17972 |
rs259006522 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78247020 | GCCCAGACACTTCTG[G/T]TTTCTCCTACCCCAG | 17972 |
rs259032217 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78245470 | GCTCTTCCATCTGCC[C/T]TTCAGACTGAAACTG | 17972 |
rs259045038 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78261336 | ATCTCTCACGATTCA[A/G]AACAGCGCAGTCTGT | 17972 |
rs259178287 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78258259 | CAGGAGTGGGAGTGG[A/C]AGGTGTAGGGATATA | 17972 |
rs259361712 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78260141 | TCTTATAAAACTAGA[A/G]TGCAGGTCTCTGGGT | 17972 |
rs259371301 | in-del | -/GGCCCTG | | | intron-variant, frameshift-variant | Ncf4 | Mm_Celera | 15:78262145 | ATCCACAGACTCAAA[-/GGCCCTG]GGAGAAGCCAGGATC | 17972 |
rs259427374 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78260576 | GTAAAGAGTGTGGGA[A/C]TCTGAGACGTGACAC | 17972 |
rs259614579 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78249430 | TCTCATTAAGTCTCT[C/G]CCCCTCCTTCATGGC | 17972 |
rs259687171 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78250575 | CTGGATAGAATTCAG[C/G]GGTGCTTCTAAACAC | 17972 |
rs259816555 | in-del | -/TAA | | | intron-variant | Ncf4 | Mm_Celera | 15:78258959 | CCCCACATCAATCGT[-/TAA]TAATAATAATAATAA | 17972 |
rs259907114 | in-del | -/GAAT | | | upstream-variant-2KB, intron-variant | Ncf4 | GRCm38.p3 | 15:78244607 | TCCACCAGACCTTAG[-/GAAT]GAATGGCAGGTCTTG | 17972 |
rs259953579 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78252996 | ATATGAGTGTGTGTG[C/T]ACCTGTACACACCTT | 17972 |
rs260014822 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78246619 | CCATGTGTAGCTCCC[A/G]TGTGCACGGAGCCTG | 17972 |
rs260037547 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78255694 | AGCAGGGCAAGCTAG[A/G]CACAGAGTTTGGATT | 17972 |
rs260122047 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78248727 | TCACTTTAACCACAC[A/G]TCAGCCCCACCCTGC | 17972 |
rs260164858 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78259886 | ATTTCCCCTTTACAC[A/G]CGTAGCCATTGACCA | 17972 |
rs260226179 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78252133 | CAACCTTTATATACC[A/C]CCCTCCTGGCATCAC | 17972 |
rs260406752 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78251844 | ATGTGAAGAGGTCCC[C/T]CATCACACCCTGTCT | 17972 |
rs260745525 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78251981 | AGCCTTCCTGAGTCC[C/T]GTCCACCTTTCTTGC | 17972 |
rs260797430 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78247691 | GGAGTAGGTGCCCAG[C/T]TCCTGGTGTGGTGTG | 17972 |
rs260805406 | in-del | -/C | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242640 | GGTGCTGGGACTGAG[-/C]CCAGGGCTTCACTCA | 17972 |
rs261040247 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78261865 | TTAGACTGGGATGGC[A/G]CATGGGGAGTTAGTT | 17972 |
rs261090241 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262490 | ATGTAAGATGCAAAC[C/T]TCCTGGCCCAGAGTG | 17972 |
rs261221224 | snp | A/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78250080 | AAACCCCTTCAGGAG[A/T]CCCAGCACACACTTC | 17972 |
rs261440163 | in-del | -/TG | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242391 | GTCTCTCTGTGTATA[-/TG]TGTGTGTGTGTGTAC | 17972 |
rs261563824 | in-del | -/TGCA | | | intron-variant | Ncf4 | Mm_Celera | 15:78259909 | TTGACCACAGAGGGC[-/TGCA]TGCTCATGTGTCCCT | 17972 |
rs261567904 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78246642 | GGAGCCTGGTATCCA[C/T]CCAACAAAACCCGTG | 17972 |
rs262064565 | snp | A/C | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78244063 | GCTCCCTACAGAACC[A/C]AGCATTAGAAGGAGC | 17972 |
rs262827281 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78260460 | CCCTAGCAAGAAAGG[A/G]CATTTCTATTAGTAT | 17972 |
rs263067282 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262416 | ACCCTGTGGCAAGGA[C/T]GGGGCGCTCAGCAAA | 17972 |
rs263296357 | snp | A/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78261766 | CCCCGGTTACCACTG[A/T]CAAGAATATTGTAAA | 17972 |
rs263324374 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78254485 | CAGATCCTTTTCCCT[C/T]TCTGATCCTAGCTTA | 17972 |
rs263388573 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78257102 | GATGGGGTTGAAGTT[A/G]GGGATGAGGATGGAG | 17972 |
rs263489777 | snp | G/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78259077 | ACTCTCTTTGTGTCA[G/T]CTTAACAGAAACCAG | 17972 |
rs263523038 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78251451 | ACACATAGCTTCTAA[C/T]CCCACCCCTGTCCCC | 17972 |
rs263714658 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78258699 | CCAAGTTCCAGCTTG[C/T]TTTCTGTCCCTGTGA | 17972 |
rs263728280 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78260330 | ACAGGAGCGTGTGAG[A/G]GTAAAATTCTTGCAT | 17972 |
rs263843666 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78254022 | CCTCAGCGCTCCAGG[A/G]TACCTGAGCCCTGTG | 17972 |
rs263939560 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78250832 | CCCACCCCGTTCTAG[C/T]TCCCCTCCCCCAGTC | 17972 |
rs264070685 | snp | C/T | | | synonymous-codon | Ncf4 | Mm_Celera | 15:78253328 | CGCAAAACAAGAGAT[C/T]GCTGAGACTCGGATC | 17972 |
rs264103292 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78246740 | AGCTCAGCTGCAGAC[A/G]GCTCACACTGGGACA | 17972 |
rs264154426 | in-del | -/CCTCTGGCTCCCCG | | | intron-variant | Ncf4 | Mm_Celera | 15:78251963 | ATTAGGCCTCCTCCA[-/CCTCTGGCTCCCCG]CCAGCCTTCCTGAGT | 17972 |
rs264260808 | in-del | -/TTCTGCCGTGAAG | | | intron-variant | Ncf4 | Mm_Celera | 15:78260601 | GACACTGGGTCTCAC[-/TTCTGCCGTGAAG]CAGCCTCTTCTTTCA | 17972 |
rs264266463 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78250359 | AAGGTGGTAACCGAT[C/T]CCCTCCCTCTGGCCT | 17972 |
rs264303251 | snp | G/T | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243403 | TCCTTGTCTTGAGCA[G/T]GGATTTGTATGCTTA | 17972 |
rs265132827 | in-del | -/TTCATTTT | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78248505 | CCTCTCCTCAGCCTC[-/TTCATTTT]TGAGATCACAGACAT | 17972 |
rs265260002 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78258641 | CAGAGACAGAGACAA[A/G]CCCTGGGACTTGCTG | 17972 |
rs265297011 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78260014 | AGTGGTGCTCGAGAA[C/T]CTCTGCTGAAGGAAA | 17972 |
rs265566955 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78253491 | CTGAAAGGCCTGGCT[A/G]GAGAGAGAAGCAAGG | 17972 |
rs265652636 | snp | C/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78249980 | TGGGGACCCAAGGAC[C/G]TCCCATGAGGCTCCC | 17972 |
rs265691029 | snp | A/G | | | downstream-variant-500B | Ncf4 | Mm_Celera | 15:78262736 | CTAAAAGTGCACAGT[A/G]GGGAGAAAAGAGTCA | 17972 |
rs265881262 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78259351 | TATATTGGATGGATC[A/C]CAGGGCCCCCAATGG | 17972 |
rs265897288 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78251816 | TCCTTGACACACCGC[C/T]CCCCTCTGGAGCATG | 17972 |
rs265933870 | snp | A/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78252899 | AGGGTGTATGTGCAT[A/G]GGCTTATGCATGTCT | 17972 |
rs265950685 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78246321 | ACTCTGCCCTTTCCA[C/T]AGCTGTTCCCCCGCC | 17972 |
rs266076803 | snp | C/T | | | intron-variant | Ncf4 | Mm_Celera | 15:78254570 | TTTCAGATGACCTCT[C/T]AAGCCAGCATCCCTC | 17972 |
rs266239591 | snp | A/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78249284 | CCAGGAAAAAAAAAA[A/C]AACAACAACAACAAA | 17972 |
rs386891287 | in-del | -/C | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78242642 | TGCTGGGACTGAGCC[-/C]AGGGCTTCACTCACG | 17972 |
rs386960344 | in-del | -/G | | | intron-variant | Ncf4 | Mm_Celera | 15:78258055 | ACTGCATGTGAGGGG[-/G]ACTGGGAAGTCTTGA | 17972 |
rs387041453 | in-del | -/AATG | | | upstream-variant-2KB, intron-variant | Ncf4 | Mm_Celera | 15:78244612 | CAGACCTTAGGAATG[-/AATG]GCAGGTCTTGGATGC | 17972 |
rs387049615 | in-del | -/CCT | | | intron-variant | Ncf4 | Mm_Celera | 15:78248309 | CTTCCTCCTCCTCCT[-/CCT]TTTCCTCCCCTTTCT | 17972 |
rs387229861 | in-del | -/TGACCCTGTGCATTAGCTC | | | upstream-variant-2KB | Ncf4 | Mm_Celera | 15:78243101 | TCAGGCTCGAGGCTC[-/TGACCCTGTGCATTAGCTC]CCTCTGTCTACCCGT | 17972 |
rs387311783 | in-del | -/AGATGGCCTTC | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78246083 | TGTTGGGTGGGGGTC[-/AGATGGCCTTC]CTTCCATAGCTATAG | 17972 |
rs387380917 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78248336 | CTTTCTCCTTCTCCT[C/T]TTTCTCCTCTTCTTC | 17972 |
rs387390902 | in-del | -/AA | | | intron-variant | Ncf4 | Mm_Celera | 15:78249283 | CCAGGAAAAAAAAAA[-/AA]CAACAACAACAACAA | 17972 |
rs387395762 | snp | A/G/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256878 | GAGGTGAGGATGGAG[A/G/T]TGAGGATGGGGGTGA | 17972 |
rs387414834 | in-del | -/CA | | | intron-variant | Ncf4 | Mm_Celera | 15:78261240 | CCTTGTACTTGGACA[-/CA]CACACACACACACAC | 17972 |
rs387567581 | in-del | -/ATA | | | intron-variant | Ncf4 | Mm_Celera | 15:78258976 | ATAATAATAATAATA[-/ATA]GTAATAGTAATAATA | 17972 |
rs387595084 | in-del | -/C | | | intron-variant | Ncf4 | Mm_Celera | 15:78247331 | CCCCACCCCCACCCC[-/C]ACCAACTGTCTTCTG | 17972 |
rs387754805 | in-del | -/AG | | | upstream-variant-2KB, intron-variant | Ncf4 | Mm_Celera | 15:78244455 | AGATTGTAAGGAGAG[-/AG]CCTCTGTGTGGATGG | 17972 |
rs387793554 | in-del | -/GGTGAGGATGGAGGTGAGGATGGGGGTGAGGATAGAGGTGAGGATGA | | | intron-variant | Ncf4 | Mm_Celera | 15:78256355 | GGTGGTAAGGATGGG[lengthTooLong]GGTGAGGATGGAGGT | 17972 |
rs387848791 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78248346 | CTCCTCTTTCTCCTC[C/T]TCTTCCTCCTCCTCC | 17972 |
rs387856673 | in-del | -/CC | | | intron-variant | Ncf4 | Mm_Celera | 15:78251765 | TCCATCTCCCCCCCC[-/CC]TTTCCTACACCCTTT | 17972 |
rs387874602 | in-del | -/CACACA | | | intron-variant | Ncf4 | Mm_Celera | 15:78261267 | ACACACACACACACA[-/CACACA]GAGCTGGGGAAATTC | 17972 |
rs578326658 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256460 | TGGGGGTGAGGATGG[A/G]GGTGAGGATGGAGGT | 17972 |
rs578529415 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78252622 | TACATATACATATGT[A/G]TATGTATATGTATGT | 17972 |
rs578541741 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78247388 | TGATGAGGGTCACCC[A/G]TGGAAAGTCCTTGGC | 17972 |
rs578740934 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78252690 | CATAGGCCTTACATG[C/T]GTATTTGCATATATG | 17972 |
rs578942207 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256948 | TGGGGGTGAGGATGG[A/G]GGTGAGGATGGGGGT | 17972 |
rs578951408 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78248328 | TTCCTCCCCTTTCTC[C/T]TTCTCCTCTTTCTCC | 17972 |
rs579121179 | snp | C/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78253230 | TTGGGGAGAAGCACT[C/G]ATTGGTGGGGCAGCT | 17972 |
rs579145429 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78261219 | GAACATCTCTCTAGC[A/G]AAAAGCCTTGTACTT | 17972 |
rs579272876 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78257050 | TGAGGATGGAGGTGA[A/G]GATGTGGGTGAAGAT | 17972 |
rs579643841 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78248381 | TCTCTCCTCCTCCTC[C/T]TCCTCCTCCTCCTCC | 17972 |
rs579811905 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256698 | TGGAGGTGAGGATGG[A/G]GGTGAGGATGGAGGT | 17972 |
rs580093985 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78259213 | ATACCCTCCCCCACC[C/T]ACTCCCCTACCCACC | 17972 |
rs580282063 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256734 | TGGAGGTGAGGATGG[A/G]GGTGAGGATGGAGGT | 17972 |
rs580394110 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78259386 | GCTAGAGAAAATACC[C/T]AAGGGGCTAAAGGGA | 17972 |
rs580620939 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256828 | TGGGGGTGAGGATGG[A/G]GGTGAGGATGGAGGT | 17972 |
rs580646544 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78246059 | GAGGTTTGTCTGTAA[C/T]AAGAGTTAGTGTTGG | 17972 |
rs580929058 | snp | A/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78259397 | TACCCAAGGGGCTAA[A/T]GGGATCCCTATAGGT | 17972 |
rs581112268 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256864 | TGGGGGTGAGGATGG[A/G]GGTGAGGATGGAGAT | 17972 |
rs581278902 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78260585 | GTGGGACTCTGAGAC[A/G]TGACACTGGGTCTCA | 17972 |
rs581473806 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256972 | TGGGGGTGAGGATGG[A/G]GGTGAGGATGGAGGT | 17972 |
rs581474412 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78261696 | TCACTCACTCACAAT[A/G]TCCCCCTGGCCATAT | 17972 |
rs581647132 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78251911 | TGTTCTGAGCCTCCT[A/G]TCCTGAGGGCTCCCC | 17972 |
rs581752174 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78257086 | TGAGGATATAGGTGA[A/G]GATGGGGTTGAAGTT | 17972 |
rs581818589 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256520 | TGGGGGTGAGGATGG[A/G]GGTGAGGATGGAGGT | 17972 |
rs581987856 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78257098 | TGAAGATGGGGTTGA[A/G]GTTAGGGATGAGGAT | 17972 |
rs582168014 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78248320 | TCCTCCTTTTCCTCC[C/T]CTTTCTCCTTCTCCT | 17972 |
rs582211629 | snp | A/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78257100 | AAGATGGGGTTGAAG[A/T]TAGGGATGAGGATGG | 17972 |
rs582376602 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78252773 | ACTGCAGGTGTATCT[A/G]TGCATATGTGTGTGC | 17972 |
rs582409767 | snp | G/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78248329 | TCCTCCCCTTTCTCC[G/T]TCTCCTCTTTCTCCT | 17972 |
rs582946359 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256840 | TGGGGGTGAGGATGG[A/G]GGTGAGGATGGGGGT | 17972 |
rs583300621 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78248525 | TTTTGAGATCACAGA[C/T]ATGTGCCACCTATGC | 17972 |
rs583350963 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78259898 | CACGCGTAGCCATTG[A/G]CCACAGAGGGCTGCT | 17972 |
rs583596367 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256710 | TGGGGGTGAGGATGG[A/G]GGTGAGGATGGAGGT | 17972 |
rs583789106 | snp | A/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78251481 | CCATCTCCTTCCCAT[A/T]TGCCCCTCGTCCCAA | 17972 |
rs583815710 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78259251 | ACTTCTTGGCCCTGG[C/T]GTTCCCCTATATTGA | 17972 |
rs583993395 | snp | A/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256794 | GGGTTGAAGTTGGGG[A/T]TGAGGATGGAGGTGA | 17972 |
rs584094240 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78259391 | AGAAAATACCCAAGG[A/G]GCTAAAGGGATCCCT | 17972 |
rs584354421 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78247383 | GAACGTGATGAGGGT[C/T]ACCCGTGGAAAGTCC | 17972 |
rs584419763 | snp | A/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78248323 | TCCTTTTCCTCCCCT[A/T]TCTCCTTCTCCTCTT | 17972 |
rs584605011 | snp | C/T | | | missense | Ncf4 | GRCm38.p3 | 15:78261028 | TCAAAGACCTGCTAG[C/T]GCTCATGAGGTGAGA | 17972 |
rs584941654 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78252813 | AGCATGTATATATAA[A/G]TTCTTGTGTATCTAT | 17972 |
rs585030042 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78257044 | TGTGGGTGAGGATGG[A/G]GGTGAAGATGTGGGT | 17972 |
rs585139187 | snp | G/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78257094 | TAGGTGAAGATGGGG[G/T]TGAAGTTAGGGATGA | 17972 |
rs585241167 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78261799 | TTCATTCACATATAC[C/T]GTCTCATTATCAAGA | 17972 |
rs585375844 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78251938 | CCCCCTTGTGCCCAG[C/T]CTCTTCCCCCATTAG | 17972 |
rs585500666 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78248378 | CTTTCTCTCCTCCTC[C/T]TCTTCCTCCTCCTCC | 17972 |
rs585613222 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256532 | TGGAGGTGAGGATGG[A/G]GGTGAGGATGGGGGT | 17972 |
rs585944132 | snp | A/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78259130 | CAATGAAAGACCCTG[A/T]TTCTTTTTATTATTA | 17972 |
rs586128202 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256722 | TGGAGGTGAGGATGG[A/G]GGTGAGGATGGGGGT | 17972 |
rs586213846 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78259381 | GAGGAGCTAGAGAAA[A/G]TACCCAAGGGGCTAA | 17972 |
rs586237639 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78259396 | ATACCCAAGGGGCTA[A/G]AGGGATCCCTATAGG | 17972 |
rs586281648 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78248330 | CCTCCCCTTTCTCCT[C/T]CTCCTCTTTCTCCTC | 17972 |
rs586438127 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256373 | GAGGATGGAGGTGAG[A/G]ATGGGGGTGAGGATA | 17972 |
rs586590432 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78251958 | TCCCCCATTAGGCCT[C/T]CTCCACCAGCCTTCC | 17972 |
rs586604057 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78250572 | TTGCTGGATAGAATT[C/T]AGCGGTGCTTCTAAA | 17972 |
rs586805967 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256852 | TGGAGGTGAGGATGG[A/G]GGTGAGGATGGAGGT | 17972 |
rs586970675 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78259985 | TGTAACTCCCGGACC[C/T]ATAGATCGGGCATAG | 17972 |
rs587174306 | snp | A/G | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78256804 | TGGGGTTGAGGATGG[A/G]GGTGAGGATGGGGGT | 17972 |
rs587455118 | snp | C/T | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78251631 | CACCTTCTGTGGGTG[C/T]GCTGTCCCCCAAACA | 17972 |
rs587566983 | snp | A/C | | | intron-variant | Ncf4 | GRCm38.p3 | 15:78245716 | ATCTGCTAAGAGCTC[A/C]AAAATGACCCAGATC | 17972 |