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 |