SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs27186454 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB | Noxa1 | Mm_Celera | 2:25097203 | ATAATGGCCAGGTAG[C/T]TTATGTTTAAGTAGA | 241275 |
rs27186455 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Noxa1 | Mm_Celera | 2:25097193 | ATGGATCACCATAAT[A/G]GCCAGGTAGTTTATG | 241275 |
rs27186456 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Noxa1 | Mm_Celera | 2:25096551 | CTCCCTCTTGCTACT[C/T]ACTGCCCCTTCCTGG | 241275 |
rs27186457 | snp | C/G | 0.124444 | 0.216185 | upstream-variant-2KB | Noxa1 | Mm_Celera | 2:25096447 | TTGCTAACCTGACTT[C/G]TTTAAGTCCTAGTGC | 241275 |
rs27186458 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Noxa1 | Mm_Celera | 2:25096341 | GTTGGTGCTCAGCAG[C/T]GCTTGTCATCCTGAG | 241275 |
rs27186459 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Noxa1 | Mm_Celera | 2:25095931 | GACTCTGCAGGACAC[C/T]CAGAAGTTGATGTCC | 241275 |
rs27186460 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Noxa1 | Mm_Celera | 2:25095757 | CGCGAGGGCTTTCTC[C/T]ACTAGTGGGCGCTGG | 241275 |
rs27186461 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Noxa1 | Mm_Celera | 2:25095683 | ATGCCATGTGGCTAG[A/G]CCTTAGAAGCCGGAT | 241275 |
rs27186462 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Noxa1 | Mm_Celera | 2:25095660 | AGCAACAAGATGGGC[C/T]GGACTGGATGCCATG | 241275 |
rs27186463 | snp | A/C | 0.336735 | 0.234472 | upstream-variant-2KB | Noxa1 | Mm_Celera | 2:25095654 | CTCTGGAGCAACAAG[A/C]TGGGCCGGACTGGAT | 241275 |
rs27186464 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Noxa1 | Mm_Celera | 2:25095575 | AAAGGAGAAACAATC[C/T]AAAGGCTGGTAGAGC | 241275 |
rs27186465 | snp | A/C | 0.231111 | 0.249285 | upstream-variant-2KB | Noxa1 | Mm_Celera | 2:25095542 | AGAGGTCAGCGTGGT[A/C]AGGCAAGTGGGCGGC | 241275 |
rs27186466 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Noxa1 | Mm_Celera | 2:25095521 | GCATTGCAGAGCTGC[C/T]TGCTCAGAGGTCAGC | 241275 |
rs27186467 | snp | A/G | 0.124444 | 0.216185 | utr-variant-5-prime | Noxa1 | Mm_Celera | 2:25095042 | AGGGCCAAGGGGACC[A/G]GGACAGCAATGAGAA | 241275 |
rs27200568 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25094299 | ACACTATCAGAGGAC[C/G]TGCAGAGCCCCTGAC | 241275 |
rs27200569 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Noxa1 | Mm_Celera | 2:25094180 | GTGTGCTCCCCTGAG[G/T]AGGTCTGCTTTGAGA | 241275 |
rs27200570 | snp | C/T | 0.32 | 0.24 | intron-variant | Noxa1 | Mm_Celera | 2:25094112 | TGAGGGCTTCTATCA[C/T]ACACCCAGGAATGGT | 241275 |
rs27200571 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Noxa1 | Mm_Celera | 2:25094060 | CTTTGCTTTCCATCT[A/G]TGGTGTCCAGGTAGG | 241275 |
rs27200572 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25093438 | TTCTTCTTATGATAG[A/T]GCATTTCAAACTCTC | 241275 |
rs27200573 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25093357 | CTTCTCAACGTTTCC[A/G]GGTCTGGCCAGTGTG | 241275 |
rs27200574 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Noxa1 | Mm_Celera | 2:25092781 | CTGCCCCAAGCACCT[C/G]ACAACAGACTCAGGG | 241275 |
rs27200575 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25092754 | AAGTGTGTTACTGCA[C/T]AGATTTCTCAGCTGC | 241275 |
rs27200576 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25092739 | CAGTTAAAGCCTGGA[A/G]AGTGTGTTACTGCAT | 241275 |
rs27200577 | snp | C/T | 0.32 | 0.24 | intron-variant | Noxa1 | Mm_Celera | 2:25092665 | ACTAAACTCAGTAAC[C/T]GAGGAACCCAAAGCC | 241275 |
rs27200578 | snp | C/T | 0.32 | 0.24 | intron-variant | Noxa1 | Mm_Celera | 2:25092452 | ACCAGAGCATTCTCA[C/T]TGAGGCTGGAGGGGA | 241275 |
rs27200579 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Noxa1 | Mm_Celera | 2:25092382 | AGCCAGGGATGTTGA[A/G]AAAGTACTATAAATT | 241275 |
rs27200580 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Noxa1 | Mm_Celera | 2:25092328 | ATCTGCAAATTGGCT[A/T]TAAATACAGTGACCT | 241275 |
rs27200581 | snp | G/T | 0.32 | 0.24 | intron-variant | Noxa1 | Mm_Celera | 2:25092316 | CCTGGTTTTCACATC[G/T]GCAAATTGGCTATAA | 241275 |
rs27200582 | snp | G/T | 0.32 | 0.24 | intron-variant | Noxa1 | Mm_Celera | 2:25092284 | AGCTGGGTAGCCATG[G/T]GTATCTTGGGATAAG | 241275 |
rs27200583 | snp | A/T | 0.32 | 0.24 | intron-variant | Noxa1 | Mm_Celera | 2:25092182 | GAAATCTCTGTCCCT[A/T]ACCAGATATTCCACT | 241275 |
rs27200584 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25092155 | CTAATCTCTGAACTT[C/T]CAACTGTGGATGAAA | 241275 |
rs27200585 | snp | A/G | 0.32 | 0.24 | intron-variant | Noxa1 | Mm_Celera | 2:25092035 | GCCACTTGAACACCT[A/G]CTCTCTGCACCTGAC | 241275 |
rs27200586 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Noxa1 | Mm_Celera | 2:25091910 | GATATTCCACCCATC[C/T]TTCTCTCTGTGTCAG | 241275 |
rs27200587 | snp | C/T | 0.32 | 0.24 | intron-variant | Noxa1 | Mm_Celera | 2:25091670 | AGAGCACCTCTAAGC[C/T]CAGTGACACTGCTTG | 241275 |
rs27200588 | snp | A/G | 0.32 | 0.24 | intron-variant | Noxa1 | Mm_Celera | 2:25091592 | AGACTACATTATAGG[A/G]CCCTTATTGCAAATC | 241275 |
rs27200589 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Noxa1 | Mm_Celera | 2:25091344 | TCCTCTGGCTCAGCT[A/G]TAGGTACTGCTGAGC | 241275 |
rs27200590 | snp | A/G | 0.32 | 0.24 | intron-variant | Noxa1 | Mm_Celera | 2:25091315 | TCTCTTCCTACTGCT[A/G]TGTTCCAACTGTTTC | 241275 |
rs27200591 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Noxa1 | Mm_Celera | 2:25091291 | TGCTACAAGGAGAGA[A/C]ACCTACCTTCTCTTC | 241275 |
rs27200592 | snp | C/G | 0.32 | 0.24 | intron-variant | Noxa1 | Mm_Celera | 2:25091193 | TATCTTAAACCCTCT[C/G]TGACAGGCAGATAAA | 241275 |
rs27200593 | snp | C/T | 0.32 | 0.24 | intron-variant | Noxa1 | Mm_Celera | 2:25090661 | TGACTGGCACTGTGC[C/T]GATGCCATGTTGTAT | 241275 |
rs27200594 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Noxa1 | Mm_Celera | 2:25090606 | TGCCTGGCACTGTGC[C/T]GATGCCATGTTGTAT | 241275 |
rs27200595 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Noxa1 | Mm_Celera | 2:25090513 | TTTGTCCATGGCAAT[A/G]TCCAGGATGTCTTGA | 241275 |
rs27200596 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25090443 | TTTTGAAGGAGTAAG[C/G]TAGAGAACCTGACCC | 241275 |
rs27200597 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Noxa1 | Mm_Celera | 2:25090366 | GGACTCCATTCATAC[A/G]TGATGATACAGGAAG | 241275 |
rs27200598 | snp | A/C | 0.231111 | 0.249285 | missense | Noxa1 | Mm_Celera | 2:25090227 | GTATCGCCTGGGAGG[A/C]TGGAAGACCTCACCC | 241275 |
rs27200599 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Noxa1 | Mm_Celera | 2:25090176 | GCGTTTTACCTTAGC[C/T]TTGCCAAGGAAATCC | 241275 |
rs27200600 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Noxa1 | Mm_Celera | 2:25090146 | AGCTGAGTCCCTGAG[C/T]TGGAAAATACCCTAG | 241275 |
rs27200601 | snp | A/C | 0.32 | 0.24 | intron-variant | Noxa1 | Mm_Celera | 2:25089736 | AGGTGGGATACTCCG[A/C]CATAGCCTGTGGTTT | 241275 |
rs27200602 | snp | G/T | 0.32 | 0.24 | intron-variant | Noxa1 | Mm_Celera | 2:25089548 | TTTGCATCAGGGCAG[G/T]TTCACAAGCAGTGTG | 241275 |
rs27200603 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Noxa1 | Mm_Celera | 2:25089479 | CAGTCTTCTGCTGTG[A/G]TAAGTGGACTCTGAT | 241275 |
rs27200604 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25089368 | TGCAGCTAAAACAAA[A/G]CAAAGCAGCCCAAAG | 241275 |
rs27200605 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25089340 | TACATCTAGCTCAAG[A/C]CTGCTGAACCACTGC | 241275 |
rs27200606 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Noxa1 | Mm_Celera | 2:25089298 | AATTCCCGGCACCTC[C/T]ATGGCTTTATGCTGC | 241275 |
rs27200607 | snp | A/G | 0.231111 | 0.249285 | missense | Noxa1 | Mm_Celera | 2:25089187 | ACCTGCTGAGGCTGG[A/G]CGTTGTGGTCATCAG | 241275 |
rs27200608 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25089146 | AGACAAAGTTAGGCC[C/T]GGATCTGCTTGCTGC | 241275 |
rs27200609 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Noxa1 | Mm_Celera | 2:25089103 | GGGCTCAAGCCCATC[C/T]GACCTAAATCTTGTT | 241275 |
rs27200610 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Noxa1 | Mm_Celera | 2:25089054 | CAGGTTACAGGAGGA[G/T]ATGTACTCTTATTCT | 241275 |
rs27200611 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Noxa1 | Mm_Celera | 2:25088999 | ATGTCTCAGGGAGAG[A/G]AGGATGTTGTGGGTG | 241275 |
rs27200612 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Noxa1 | Mm_Celera | 2:25088929 | GTTGTTGAGGAAGCT[G/T]CCTGTTCTCTCAGCT | 241275 |
rs27200613 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25088847 | TGGTGGGTTTCAATG[A/T]GTGCCAGTGAGTAGG | 241275 |
rs27200614 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25088831 | CACCATCTGGTCCCT[G/T]TGGTGGGTTTCAATG | 241275 |
rs27200615 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25088768 | CCAGACTATCAAGTG[A/G]TCTGATCACCACACA | 241275 |
rs27200616 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Noxa1 | Mm_Celera | 2:25088758 | CTATCTTTCCCCAGA[C/T]TATCAAGTGGTCTGA | 241275 |
rs27200617 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25088728 | GGAAGGAAGACATTG[C/T]TTGGTCCTTCCGACC | 241275 |
rs27200618 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25088663 | TCCAGGGAAGCAAGG[A/G]TTCCTGCCTAACTCC | 241275 |
rs27200619 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25088323 | AGAGTCTTAGGAGGT[G/T]CCCAGCCTAGGGTGC | 241275 |
rs27200620 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Noxa1 | Mm_Celera | 2:25088043 | GCAGAAACTCCCTGG[A/G]CTCTGTCCTAGCACG | 241275 |
rs27200621 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25087793 | TGCATCCTTGAGTGC[C/T]CTTGTTAAAGGATGC | 241275 |
rs27200622 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25087505 | CACGAGCATTTTGTA[A/G]GTAAGGGTAAAGTAT | 241275 |
rs27200623 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Noxa1 | Mm_Celera | 2:25087504 | ACACGAGCATTTTGT[A/G]GGTAAGGGTAAAGTA | 241275 |
rs27200624 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25087420 | TTCAGGTGTGATAGG[A/G]GCTACACTCTTCTAC | 241275 |
rs27200625 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25087378 | AACACATACCAGGGC[G/T]TTTACTATTTACATT | 241275 |
rs27200626 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Noxa1 | Mm_Celera | 2:25087228 | CAGTGGTCAAAGGGA[C/T]CTCACAAGTGTGGGT | 241275 |
rs27200627 | snp | A/G | 0.231111 | 0.249285 | missense | Noxa1 | Mm_Celera | 2:25087156 | AGGACCCTCTTACAC[A/G]TAGATGAGGATGGCT | 241275 |
rs27200628 | snp | C/T | 0.124444 | 0.216185 | intron-variant, synonymous-codon | Noxa1 | Mm_Celera | 2:25087131 | GAGGCTCCTCCTACC[C/T]GTAGTGCTCAGGACC | 241275 |
rs27200629 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Noxa1 | Mm_Celera | 2:25086811 | CTTAGCCTTTGAAGG[A/C]AGGTTTATTCTTGGA | 241275 |
rs27200630 | snp | C/T | 0.124444 | 0.216185 | missense | Noxa1 | Mm_Celera | 2:25086768 | CAGGGTCCTTTGTAG[C/T]TGCTCCCTGAGGACA | 241275 |
rs27200631 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Noxa1 | Mm_Celera | 2:25086666 | GGGCTTGAGCTAGTA[A/G]TGTCTGAAAACTGGA | 241275 |
rs27200632 | snp | A/C | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Noxa1, Entpd8 | Mm_Celera | 2:25086146 | TTCCAACTGTCTGGG[A/C]TGCCCACAGCAGGCA | 241275 |
rs27200633 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, downstream-variant-500B | Noxa1, Entpd8 | Mm_Celera | 2:25086043 | TTGGGCACGATAGTT[A/G]TACTGAGCTACTACT | 241275 |
rs27200634 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon, downstream-variant-500B | Noxa1, Entpd8 | Mm_Celera | 2:25085983 | TTTACCTTCACACAG[A/G]ACATCCACCGTGTCC | 241275 |
rs27200635 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, downstream-variant-500B | Noxa1, Entpd8 | Mm_Celera | 2:25085850 | CTCCAGCCATGCTTC[A/G]TCCACTGTGGAGACA | 241275 |
rs27200636 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, downstream-variant-500B | Noxa1, Entpd8 | Mm_Celera | 2:25085814 | CTTAGGGAAAATGCC[A/G]ACGCAGCCATCTCGG | 241275 |
rs27200637 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon, downstream-variant-500B | Noxa1, Entpd8 | Mm_Celera | 2:25085778 | GGCTTCCACATAGGC[A/G]CCAGCTGGGACCACA | 241275 |
rs27200638 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B, utr-variant-3-prime | Noxa1, Entpd8 | Mm_Celera | 2:25085661 | AAGTTGGGAATGAGG[A/G]AATCATTTTTGTTTG | 241275 |
rs27200639 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B, utr-variant-3-prime | Noxa1, Entpd8 | Mm_Celera | 2:25085590 | GGCCAGCCCAGCTTC[C/T]TCACACAAGAGCCTG | 241275 |
rs211789796 | snp | C/T | | | intron-variant | Noxa1 | Mm_Celera | 2:25093270 | ACTACAGCTTCACAC[C/T]GACACGTTCAAGTGC | 241275 |
rs211853838 | snp | C/T | | | intron-variant | Noxa1 | Mm_Celera | 2:25093864 | TACTTGCCACCATGC[C/T]TAATGACCTGCGTTT | 241275 |
rs212144854 | snp | A/C | | | upstream-variant-2KB | Noxa1 | Mm_Celera | 2:25095280 | AACCACGGTTATCTC[A/C]ATATGGACACGCCTT | 241275 |
rs212415157 | snp | C/T | | | upstream-variant-2KB | Noxa1 | Mm_Celera | 2:25095909 | ACAGGTGGGGCAGCC[C/T]AATGTAGACTCTGCA | 241275 |
rs212473975 | snp | C/T | | | intron-variant | Noxa1 | Mm_Celera | 2:25088262 | TCTTCTATCAATCCT[C/T]AAATCTCAATGCTGG | 241275 |
rs213003549 | snp | A/G | | | intron-variant | Noxa1 | Mm_Celera | 2:25089413 | AACATTTGTGCTAAT[A/G]ATATCAACTTAATTT | 241275 |
rs213070937 | snp | A/T | | | intron-variant | Noxa1 | Mm_Celera | 2:25090384 | ATGATACAGGAAGTA[A/T]GAGGCACCCAGGCTA | 241275 |
rs213342940 | snp | C/T | | | intron-variant | Noxa1 | Mm_Celera | 2:25091364 | TACTGCTGAGCCAAA[C/T]CCTTTCCCCCTAAAC | 241275 |
rs213516759 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Noxa1, Entpd8 | Mm_Celera | 2:25085581 | CAGCTCTGGGGCCAG[C/T]CCAGCTTCTTCACAC | 241275 |
rs213572442 | snp | A/G | | | intron-variant | Noxa1 | Mm_Celera | 2:25092374 | AGGGAGAGAGCCAGG[A/G]ATGTTGAGAAAGTAC | 241275 |
rs213901131 | snp | A/C | | | intron-variant | Noxa1 | Mm_Celera | 2:25093911 | ATGGGAAAGAGAAAA[A/C]TGACTCCCACAAGTT | 241275 |
rs213956787 | snp | A/G | | | intron-variant | Noxa1 | Mm_Celera | 2:25086882 | AGAATCTGAGATATG[A/G]CCTTCCTTGCTCCAA | 241275 |
rs214196888 | snp | A/C | | | intron-variant | Noxa1 | Mm_Celera | 2:25087542 | GGTAAGACACTTGGC[A/C]AAGTTTCAATAGAGT | 241275 |
rs214448011 | snp | G/T | | | synonymous-codon | Noxa1 | Mm_Celera | 2:25094750 | CTGGGGTGCTTACCC[G/T]CAGCGCAGCCTCGGG | 241275 |