| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs245205524 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152822920 | GCAATAGTGGCATGC[C/G]TGCTCCGGGGTAACC | 17970 |
| rs245301076 | snp | C/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799525 | AACTCAGAAATCCAC[C/T]TGCCTCTGCCTCCCA | 17970 |
| rs245309031 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815368 | GGGTGCGGCCTGTTT[C/T]GACTCCTCCCTCTCA | 17970 |
| rs245347921 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820546 | TCACCCCCTTCCCTG[A/G]TGCCATTAAAGTGTT | 17970 |
| rs245378045 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152819057 | GTGTTGTACCCGTGT[A/G]CTCACAGACAAGCAG | 17970 |
| rs245455907 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152817111 | TGAGGTGAGGAGGGC[A/T]GGGATGGCCCGCGAG | 17970 |
| rs245489702 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827731 | TCAGTGAAAGCTCTC[C/T]AGATTCCACGAGCTA | 17970 |
| rs245579874 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152804051 | AACAAGAATAATGGC[A/G]GCTTAATTAACATTA | 17970 |
| rs245593746 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809186 | GACCCCAAATCTCTG[A/G]GATTGCACAGCAAGT | 17970 |
| rs245746941 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152833464 | CTACCTGACTCTCCA[G/T]CTACACGTCATCCTA | 17970 |
| rs245785365 | in-del | -/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812900 | ATTATTTTTCTCAGA[-/T]TTTTTTTAAGGTTCT | 17970 |
| rs245829606 | in-del | -/AA | | | intron-variant | Ncf2 | Mm_Celera | 1:152804553 | TTTGCTCCATCCACC[-/AA]GTGTGTACATGTGCA | 17970 |
| rs245913050 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152800652 | AACCCTGCCTTCATT[A/G]CGATGTTTCTGTCGG | 17970 |
| rs245970285 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819122 | CCTTCAAAGGTAGGG[G/T]TGTCTAACCTGATAT | 17970 |
| rs246041713 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152809142 | TCTGTGGAGTTCCCT[C/T]CTTCCATTTTGACCT | 17970 |
| rs246118348 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826663 | GGGGCAGAAAGAGGG[C/T]CAGCATCTAGATTCC | 17970 |
| rs246132046 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825649 | ACTTAAAATGGTCAA[C/T]TTGATGATTTGATGT | 17970 |
| rs246141961 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152805181 | GGGATAGAGATCTTG[A/G]TGAGTGCAGGACACA | 17970 |
| rs246189946 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152832219 | CCTGGTGAGCTTCAG[A/C]AGATGCTCCAGTAGA | 17970 |
| rs246211178 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806671 | CAGTGTCAAGGATCT[A/G]AGACTTAAAGACACT | 17970 |
| rs246264957 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806297 | GCTGCCGCTGCCGCT[A/G]CTGCTAAGGAGGAGG | 17970 |
| rs246268996 | in-del | -/GAAC | | | intron-variant | Ncf2 | Mm_Celera | 1:152828278 | GGGCAGGGCTGAGCA[-/GAAC]GAACATCCCCATCCC | 17970 |
| rs246286629 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152801531 | GAATCCACATTTAGG[A/G]TCTCAATTGTTTATT | 17970 |
| rs246288481 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152832142 | CACTGGATGGTGTGG[A/G]TGGAAGATCTTCCCA | 17970 |
| rs246317442 | in-del | -/TGT | | | intron-variant | Ncf2 | Mm_Celera | 1:152800939 | ACTGAAAAGGATGAC[-/TGT]AGCCCCAAAGAGAGC | 17970 |
| rs246431371 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802604 | AGGTGTGCGCCACCA[C/T]GCCCGGCTGATCACA | 17970 |
| rs246545683 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825525 | GGAGACTGTAGTCTT[C/T]TTAGTAGTTCCAACA | 17970 |
| rs246614904 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820667 | AGGAGCTTCAGTTGG[A/G]GAAGTGCTTCCATGA | 17970 |
| rs246616683 | in-del | -/AGAT | | | intron-variant | Ncf2 | Mm_Celera | 1:152833257 | TGTTAAAGGGTAGGG[-/AGAT]AGATGGGCACTGTGG | 17970 |
| rs246826114 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152820443 | AATATGTACAAAAGT[G/T]TAGTTGGTTCTTGTA | 17970 |
| rs246884067 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826904 | GTAGCTGTCTTCAGA[C/T]ACTCCAGAAGATGGC | 17970 |
| rs246937205 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152802776 | AGTCACTATTTTATG[A/G]TTCTACAAGATCATT | 17970 |
| rs247046790 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152817838 | GGCTTTGACTTGTGA[G/T]TTTATGAACTTTTCT | 17970 |
| rs247059722 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152822444 | CAAGATACCACACAG[A/G]ATGGAAAAGAGTCAG | 17970 |
| rs247093103 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806294 | gctgctgccgctgcc[A/G]ctgctgctAaggagg | 17970 |
| rs247100733 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152833009 | ACATAGTGTGCATTT[C/T]AGACCATAAACACAC | 17970 |
| rs247114798 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806548 | ACTAGATTGCCCAAG[A/G]CAGGTCTTGAATTTG | 17970 |
| rs247214865 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152827768 | TCTCTTTCCTGTGTG[C/G]GTTTTTTCTAAAGCA | 17970 |
| rs247225228 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152833670 | AACACCCCCCTTTCC[C/T]TGAGGCACTCCTGGT | 17970 |
| rs247226620 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152827487 | TTTAGGTCTGCATGC[A/G]AAATACCCTCACTCT | 17970 |
| rs247246271 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152829572 | TAACAGGGAAATGAG[C/T]AAGGTACAGAGGCTC | 17970 |
| rs247252883 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152811012 | AGAAGTAAGTGGTCC[A/G]CTGCCACTCAGGCTG | 17970 |
| rs247292451 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152803665 | GACTTCATGCTGTTA[C/T]AGAGTTTTGCTCTGC | 17970 |
| rs247292534 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152809220 | TTTGTCTGCTGAACT[A/C]GATCTCACAGCTCCG | 17970 |
| rs247348740 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808937 | CTAAAACACAGTCTA[C/T]AGATCAGGCTGGTTT | 17970 |
| rs247374910 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152804108 | GGATTGAGGTGATCA[A/G]ATGATAATTAATTTC | 17970 |
| rs247399807 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816244 | AAGACACGATTGTAC[C/T]GTTAGTGCTGATGAC | 17970 |
| rs247416463 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152805423 | GGCTTGGGGTCTGAG[A/T]CAGGATCAGGAGAGA | 17970 |
| rs247422147 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152835936 | ACTAATAGGGTCAAT[A/G]GACCACTCACGATGG | 17970 |
| rs247478412 | in-del | -/GAG | | | intron-variant | Ncf2 | Mm_Celera | 1:152811533 | ATAGATAGATAGATA[-/GAG]TTTACAGTTGATGGC | 17970 |
| rs247484348 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152835697 | TGATGAACCTTATGG[C/T]GCTTACCACCATGCC | 17970 |
| rs247499553 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152810759 | GGTAATTTACCACAG[A/G]CTATGCAAAGAGGAA | 17970 |
| rs247570830 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816270 | ATGACACTTAAAGTG[C/T]CCCCTCTGAGATTGT | 17970 |
| rs247720293 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152823732 | AGTCTGGTCTACATC[A/G]TGAGCTCTAAACCAG | 17970 |
| rs247740105 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152811751 | CCAAATCAAACAAAA[A/C]ACCCAAAATGAGTGT | 17970 |
| rs247740751 | in-del | -/AAAAACAAGCAA | | | intron-variant | Ncf2 | Mm_Celera | 1:152828707 | CACCCCCCTTGTCTG[-/AAAAACAAGCAA]AGAAACAACTCTAAG | 17970 |
| rs247879551 | snp | A/G | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800171 | TCAGCACTCTCCCGG[A/G]GGTCCCTGACTCTGG | 17970 |
| rs247928373 | in-del | -/TAAT | | | utr-variant-3-prime | Ncf2 | Mm_Celera | 1:152836449 | AGTTCAGTGGAAAAA[-/TAAT]TAATAAAGGGTTCTT | 17970 |
| rs247948679 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815477 | TACCAAGGGGTCCCT[A/G]TGGGGTTGGTGACAG | 17970 |
| rs247967638 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152829814 | TTTTCTTTTTTTTCC[A/G]AGACAGGGTTTCTCT | 17970 |
| rs247969713 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152823273 | TATGTTACATCCTAT[C/T]ACCAAGGCTCAGGGC | 17970 |
| rs247981655 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152829037 | GTAAGTAAAAGGCCC[A/G]GGGCAGGGGGAGTAG | 17970 |
| rs248025231 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152828138 | TCAGGAAAAGTGTGT[A/G]TGGGTGGGTGGTGGG | 17970 |
| rs248068237 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152805150 | GGGAGTGGCCCTTGC[A/G]GCTGGGACACAAGGA | 17970 |
| rs248123540 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152810249 | CTTCTACCCTTACTG[C/G]TCAAGATCTTTCTTT | 17970 |
| rs248151104 | snp | A/C | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799563 | GGATTAAAGGCATGC[A/C]CAACTACTGCCAGGC | 17970 |
| rs248440580 | snp | C/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798343 | AACAGGTTCAGTTGA[C/G]CCAACTACACGAATG | 17970 |
| rs248495028 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152816728 | GTTTGAAGGTCACTC[-/A]AGGTCATCAGAAAGG | 17970 |
| rs248498404 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808804 | TCAAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 17970 |
| rs248541981 | in-del | -/ATTTGATG | | | intron-variant | Ncf2 | Mm_Celera | 1:152825648 | CACTTAAAATGGTCA[-/ATTTGATG]ATTTGATGTTGTATG | 17970 |
| rs248567516 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152834721 | TCTGCCGCTCCCCCC[A/C]CCCCCATATGATAAA | 17970 |
| rs248567936 | snp | C/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814128 | GCTTGGAATCAAACC[C/G]CAGTCTTCAGTGAGA | 17970 |
| rs248646693 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806508 | CTCTGAACTACTCAA[-/T]TTTTTTATATTAAGA | 17970 |
| rs248738653 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152829194 | CATGAGACGCTCAGA[-/G]GGGGGAGAAGCTGTC | 17970 |
| rs248785430 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152829594 | AGAGGCTCACGTTTC[-/T]TTTTTTTTTTTTCTT | 17970 |
| rs248912905 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826805 | GCAGAACAGGGAATA[G/T]ACATTAAAGAGAGAC | 17970 |
| rs248997398 | in-del | -/TTTTTTC | | | intron-variant | Ncf2 | Mm_Celera | 1:152832817 | CTCATAGTTTTTTTT[-/TTTTTTC]CTTACCTTTTCTGTC | 17970 |
| rs249031182 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152831413 | TGCCATGTCACCTGA[C/T]GCTGATGGGTTTTCA | 17970 |
| rs249088746 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152818449 | AAGTCCTTCACAGGA[A/G]GACGTTTTCCCTGTT | 17970 |
| rs249165311 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826169 | CTTGCGCAGCCTCTG[C/T]ACTCAGGAAGTTTTG | 17970 |
| rs249171252 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152804061 | ATGGCAGCTTAATTA[A/G]CATTAGCTCACCTGC | 17970 |
| rs249194352 | in-del | -/AAG | | | cds-indel, intron-variant | Ncf2 | Mm_Celera | 1:152807742 | GTGCCCAGGACATAG[-/AAG]AAGCTCTTAGAGGAA | 17970 |
| rs249217896 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802202 | TATTTGGGCTCTTTA[C/T]TCTTTGACTCAGGCC | 17970 |
| rs249234385 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152836618 | ACCATCCAGTCCCAA[A/G]GAGAATGGAACTCTT | 17970 |
| rs249259189 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152824093 | ACATATTCCACAATG[A/G]TTGAACCACCAAGGT | 17970 |
| rs249267983 | in-del | -/ATTT | | | intron-variant | Ncf2 | Mm_Celera | 1:152830043 | TGCTAAGGGAAAGGA[-/ATTT]ATTCTGGACCTGCTG | 17970 |
| rs249319176 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152831807 | TGCACCTTGCTTTAC[C/T]TAGCATGCTCCTTGT | 17970 |
| rs249364542 | in-del | -/TGCA | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814027 | TGAATGTGTAGCATG[-/TGCA]TGCCTGAGGCCCATG | 17970 |
| rs249382152 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152822405 | TTGGCTCTTGAGTGT[A/G]CCCTCTATGCTGGGA | 17970 |
| rs249440588 | snp | A/T | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800371 | GTCGGTGTGAAGCTT[A/T]GTGTTTCGAGCTTGA | 17970 |
| rs249454033 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812565 | AGAAAAGAAGAAAGA[A/G]AGAGAGAAAAAGAAA | 17970 |
| rs249483417 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152805922 | CTTGATTGCTGATAC[C/T]CTAAGGACAGAGAGT | 17970 |
| rs249509364 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152811154 | ATGCAAGGAGTAGTA[A/T]GCAAGAGGCTTTTCT | 17970 |
| rs249509424 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152804422 | TGCTTAGTCACAAAC[A/G]TTTGTGGGTTCTTAA | 17970 |
| rs249595939 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152822597 | TGCGGGGGGGGGGGG[A/G]GTGTCTCCTGGATAC | 17970 |
| rs249611472 | in-del | -/TGTTTC | | | intron-variant | Ncf2 | Mm_Celera | 1:152822048 | GTGTTTTTTTTTTTT[-/TGTTTC]TTCTTTATTTGGAGA | 17970 |
| rs249671346 | in-del | -/AGT | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800507 | GCATAAAGAGAAGAA[-/AGT]GGCTACGTGAGTATG | 17970 |
| rs249712884 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819668 | CACCAGCTACTTAGT[C/T]GTGCTGAACTAAACT | 17970 |
| rs249795957 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152818097 | CCCGTCCTGCTCTGT[A/G]GCAGGCACACAGCTA | 17970 |
| rs249806716 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818178 | CTGAGGCTGGTTCCC[G/T]GAGGACAGGGGTTAT | 17970 |
| rs249837171 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813119 | CTCAGATTTTTTTTT[A/T]AAAGATTTATTTATC | 17970 |
| rs249865043 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152828401 | GAGGGGTCAATGAAG[C/G]GGAAAGGACATGGCT | 17970 |
| rs249941594 | in-del | -/CT | | | intron-variant | Ncf2 | Mm_Celera | 1:152809241 | ACAGCTCCGCGGGAG[-/CT]CTTCACCTGCTTCTT | 17970 |
| rs250041174 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804888 | CCCTCACGCTGACTC[G/T]GGAGACAAGAACTTG | 17970 |
| rs250061472 | in-del | -/TAGA | | | intron-variant | Ncf2 | Mm_Celera | 1:152811515 | TTAAATATGTGTGTT[-/TAGA]TAGATAGATAGATAG | 17970 |
| rs250087316 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152836787 | GCTGGGATTAAAGGC[A/G]TGCGCCACCACTGTC | 17970 |
| rs250189460 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818169 | TGGCTGGCCTGAGGC[-/T]TGGTTCCCTGAGGAC | 17970 |
| rs250198029 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827350 | AGTCTGTTCTCTCTT[C/T]CCCCCCCGCCCCCTC | 17970 |
| rs250242322 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152800897 | TGGGATAGCGTGTGG[G/T]GGTTCAGCATTCTGA | 17970 |
| rs250259251 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152817146 | GCACAAAGGTCTAGC[A/T]GTTGTGACAGCAGCT | 17970 |
| rs250287143 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152820744 | GCCCCTTGTGGGTGG[G/T]ACCATCTCTGGGCTG | 17970 |
| rs250336696 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152811173 | AGAGGCTTTTCTGGG[A/G]AGGGGAGGCAAGCCT | 17970 |
| rs250354753 | in-del | -/GGCTTGG | | | intron-variant | Ncf2 | Mm_Celera | 1:152827155 | GAAGGGTTGAGTTGA[-/GGCTTGG]GGTCAATAAAACCTT | 17970 |
| rs250380065 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152803582 | TAGAACTGATGGAGT[A/G]TGGCCCACCAGTTAG | 17970 |
| rs250534705 | snp | C/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799804 | CTACAACAGAGGAAT[C/T]AACAGAGAATCTTAG | 17970 |
| rs250556801 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152832500 | AATCAACACCACAAA[A/G]GAGCATGGCTTGCCT | 17970 |
| rs250596558 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808496 | TAAAGTTTCTCTGCA[-/T]CCATAAACCCTTGTA | 17970 |
| rs250597551 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152833212 | TGCTCACACATTTGC[A/G]CTCTCTATGCTCCTC | 17970 |
| rs250615732 | in-del | -/GAACT | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813914 | TGGGGCTAGCTTTAG[-/GAACT]GAACCCAAGGGTTTT | 17970 |
| rs250652658 | in-del | -/TGCTTGAAAATTTT | | | intron-variant | Ncf2 | Mm_Celera | 1:152804478 | TTGTGATTTTTGTAC[-/TGCTTGAAAATTTT]TGCTTGAAAATTTTT | 17970 |
| rs250654254 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152832695 | AGAAGTCCCCTGGGA[A/G]CAAGCATGGCTTCTG | 17970 |
| rs250659276 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808869 | GCCCGGAGTTGAACA[G/T]GCTCGATTCTCTTTA | 17970 |
| rs250724116 | in-del | -/AAAC | | | utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152837565 | AACAAAAAAACAAAA[-/AAAC]AAAAAAAGAAAAAAG | 17970 |
| rs250755071 | snp | C/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814074 | GTACCAGATCCCCTC[C/G]GACTGGGGCTATGGA | 17970 |
| rs250789136 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809039 | GCCTCTTGATTGCTT[A/G]GGTGTGTGTGTGTGT | 17970 |
| rs250798194 | in-del | -/CTTTTT | | | intron-variant | Ncf2 | Mm_Celera | 1:152816077 | CTGGGTAACTTGTCC[-/CTTTTT]TTTTTCTAAAACAAA | 17970 |
| rs250817502 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152831854 | CTTGCTTTATGACTA[C/T]ATTTTTCCAGAGCCC | 17970 |
| rs250849135 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814473 | CTCAAGGCAACATTT[A/G]ATCAGGCTGGCATAC | 17970 |
| rs250880010 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152830131 | CATCGTGGTGTTCCC[C/T]GGGAGAAGGGGAACT | 17970 |
| rs250894613 | in-del | -/GCCAGC | | | intron-variant | Ncf2 | Mm_Celera | 1:152820259 | GGGTTGATCCTGGCT[-/GCCAGC]GCCAGCGCCAGCACC | 17970 |
| rs250961699 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820883 | GAGTTCTAGTCCTGA[C/G]TTCCTGTGGTGATAC | 17970 |
| rs250977443 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152802004 | GAGAGGCAGAGCAGA[A/G]GTTGATGATCTCTGG | 17970 |
| rs250987296 | snp | G/T | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152807272 | AGACTAGTGAACTCA[G/T]TAGTCATCAACACGA | 17970 |
| rs250988045 | snp | C/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815557 | GTGTGGCTGTTTCTC[C/G]GCAGATGTCTTAGGA | 17970 |
| rs251064857 | in-del | -/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813825 | GTTAATTAGCCAAAA[-/G]GGGGGGGCTTTAATA | 17970 |
| rs251069012 | in-del | -/GGGGG | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813824 | GTTAATTAGCCAAAA[-/GGGGG]GGGGGGGGCTTTAAT | 17970 |
| rs251073183 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152800774 | AGATGTCCTCGGTGC[A/G]AGAGTCCTTGCCTGA | 17970 |
| rs251078033 | in-del | -/ATGT | | | intron-variant | Ncf2 | Mm_Celera | 1:152811852 | CACACACACACACAC[-/ATGT]ACACACAGATATATC | 17970 |
| rs251197651 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152820583 | GGCTCTGTGCATGCT[G/T]ACTCTCTTTCTACCT | 17970 |
| rs251238401 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152811622 | AGTCTGGAAGGGCAT[C/T]GGCCAATGCACTATT | 17970 |
| rs251281354 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152802924 | TTTTCTGTCCTTGCA[A/C]CTACAATAAATTGCC | 17970 |
| rs251306288 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813254 | CACGTCTAAGAAGAA[A/C]CTTTGAAGGTCTATG | 17970 |
| rs251477235 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152815902 | CATTCAAGAGGTAGA[A/C]GCAGAAGGACCAGAA | 17970 |
| rs251541241 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152820610 | ACCTTGTCCTGGCTG[G/T]TTTTGTGTCAACTTG | 17970 |
| rs251595383 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152811718 | CAGGCTATTTACTGT[C/T]GTAAGTAAAAAGAAA | 17970 |
| rs251638887 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152834724 | GCCGCTCCCCCCACC[C/G]CCATATGATAAAAAC | 17970 |
| rs251682297 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152829223 | TCTGTGCAAGCCTGG[C/T]GACTCACTGCGCTGG | 17970 |
| rs251693082 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152835336 | AGGCAAAAGCAAATG[C/T]GTGGCTTTCTCCTGT | 17970 |
| rs251742036 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152803166 | ATCAGGAATTATGAA[A/C]TCATCAGTTCATCTA | 17970 |
| rs251757341 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152810302 | CTCATCTCATCTGTC[A/G]TAGTCTTTCTGTTTA | 17970 |
| rs251850794 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826266 | GGGGGCTTTGACTTC[C/T]TTGGTGCTGTCCATT | 17970 |
| rs251915395 | in-del | -/CTCT | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800192 | CTGACTCTGGCTGTG[-/CTCT]CTCTCCCACACAGCT | 17970 |
| rs251965173 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816212 | AAACCACCTGCTCAG[C/T]CAACTCTGCAGGGAG | 17970 |
| rs251993500 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827879 | AGCCAGGCGTGGTGG[C/T]GCACGCCTTTAATCC | 17970 |
| rs252041909 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152824339 | GGTAGGTGGGCCGTC[C/T]ATCTTCCTACTTCTC | 17970 |
| rs252052706 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152816832 | GTGCTGGTTAGCCCC[A/G]GTGTGCAAAAGTCAT | 17970 |
| rs252066345 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818125 | CTACGCCATTGCTCA[C/T]AAGGGAAGACTTGCA | 17970 |
| rs252149460 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152802090 | CTCTCTCTTGGTATT[A/G]GGGGCGGGAGTTGGG | 17970 |
| rs252213474 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822845 | GGGAGAAAAGTCTTA[C/T]TCAGCTGTGAGCCTG | 17970 |
| rs252233563 | snp | A/C | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800397 | CTTGACAGGATCTAG[A/C]TGAGCCTCAGGTCAC | 17970 |
| rs252244090 | snp | C/T | | | synonymous-codon | Ncf2 | Mm_Celera | 1:152833854 | CATGGAGACGCGGCT[C/T]GGCCTCCCCTACAGC | 17970 |
| rs252266510 | in-del | -/ACACACACACACACATACACACACACACACACAC | | | intron-variant | Ncf2 | Mm_Celera | 1:152825332 | GTGCCCCCAGGCATA[lengthTooLong]ACACACACACACACA | 17970 |
| rs252283733 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152823428 | AGAGGATTAAGTCAG[C/T]CAACCTTCTAGGTTG | 17970 |
| rs252380535 | snp | C/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799505 | CGTAGACCAGGCTGG[C/T]CTCGAACTCAGAAAT | 17970 |
| rs252418561 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806001 | GGGGTAAAGACACAA[A/G]AGCATATGTAACTGC | 17970 |
| rs252419507 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152824851 | GAGTTGCCCAATCTG[A/G]GTAAGCTAGACCTGG | 17970 |
| rs252419566 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799890 | GCTTAGGTGGCTATA[A/G]CATATCAAAGCAGAG | 17970 |
| rs252421888 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152809279 | TTGTTGTTTTCTAGG[A/T]AGGGTCCCTGTCTTA | 17970 |
| rs252470641 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152805343 | AAGTCATTCCCAATT[A/G]GTTAATAAAGATTCC | 17970 |
| rs252513314 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808969 | GAACTCACAGAGATC[C/T]GCCTGCCTCTGCTTC | 17970 |
| rs252568387 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818084 | GCGTGGCCCATGGCC[C/T]GTCCTGCTCTGTGGC | 17970 |
| rs252586985 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819267 | ttagaacccatcttt[C/T]cttccttcctttctt | 17970 |
| rs252587139 | snp | A/C | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799569 | AAGGCATGCACAACT[A/C]CTGCCAGGCTTAAAT | 17970 |
| rs252614266 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818068 | CTGAGTCCCTGGGGA[C/T]GCGTGGCCCATGGCC | 17970 |
| rs252622975 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152832484 | AAAACAGGAACTGGA[A/G]AATCAACACCACAAA | 17970 |
| rs252848065 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152808352 | GTTTTAAAAGCTCCC[A/G]GGGCAGGTTTTCAGA | 17970 |
| rs252895498 | in-del | -/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814636 | AGACCTCAAGCCCCA[-/C]CCCCACAGTGACCCT | 17970 |
| rs252923324 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827053 | CTCTTGTCTGGCCAG[G/T]GGATGCTGAGTTGAT | 17970 |
| rs253078610 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804343 | CAAACCGCAGCCTGC[C/T]AGTAAGAGAACCTGG | 17970 |
| rs253094395 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813683 | GGGAAGGGATGTTTG[A/C]CCCAGAGGGGCAAAG | 17970 |
| rs253107207 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152802894 | TCTTGTATAGGTAAA[A/C]TAGTTCATCACTTAT | 17970 |
| rs253140429 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826330 | AGGCAGGCTGCCAGC[C/T]CAAGCTGGGCTCAGA | 17970 |
| rs253153653 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804799 | CATCCCCGACTTGGA[C/T]TGGGGACAGACTGTC | 17970 |
| rs253163626 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152826232 | GTTGCAGGGGATAGG[A/G]TGCCAGGGCTTGGAG | 17970 |
| rs253165902 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152818801 | TTAATCTCAGCACTC[A/G]GGAGGCAGAGTCAGG | 17970 |
| rs253187897 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802985 | AGAGTGGCCTCATTC[C/T]TAACCTACAAGAATG | 17970 |
| rs253331727 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152831186 | GGAAGCCATATGCTC[C/T]TAACACATGGGATGT | 17970 |
| rs253360570 | snp | G/T | | | utr-variant-5-prime, intron-variant | Ncf2 | Mm_Celera | 1:152807709 | CCACAGAGGGTGTGG[G/T]AAGCAGACATGTAGG | 17970 |
| rs253402529 | snp | A/G | | | synonymous-codon | Ncf2 | Mm_Celera | 1:152825938 | CGCCCCTCTGCAGCC[A/G]CAGGTGAGACTGGCT | 17970 |
| rs253408285 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152803975 | TAGAGAATCTTGGGG[-/A]ACATTTGGAAAGGCA | 17970 |
| rs253467134 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809122 | TGTGTCAATCAAAGG[A/G]CGACTCTGTGGAGTT | 17970 |
| rs253498009 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152829476 | CAATGGACCCAAAAC[A/G]CAAGGGTAGTACTGA | 17970 |
| rs253499774 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806611 | agggtggcaggcctc[C/T]gccatcaggctagac | 17970 |
| rs253513818 | snp | C/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812446 | TCCCAGCAACCGCGT[C/G]GTGGCTCACAACCAT | 17970 |
| rs253535942 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806501 | ACCTCTAGCTCTGAA[C/T]TACTCAATTTTTTAT | 17970 |
| rs253652619 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152816585 | AGCTATAGCTGTAAC[A/G]AGGAACCCCTGGCAG | 17970 |
| rs253658908 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152816505 | GGAGGGGGCAAGAGG[C/G]CACAAACCTCAAACT | 17970 |
| rs253697798 | in-del | -/CTGC | | | intron-variant | Ncf2 | Mm_Celera | 1:152808238 | GTAATTATAGCCTTT[-/CTGC]CCGCCTCTGGAAACC | 17970 |
| rs253764419 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812508 | tgcaggcatacatga[A/G]ggcagaatgctgtat | 17970 |
| rs254027953 | in-del | -/TTTT | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813474 | GCTATCAGGCTTGGC[-/TTTT]TTTTTTTTCTTTTTC | 17970 |
| rs254035568 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152805075 | TGTGGGTCATGGCGG[C/T]CAGTTGGGGAAGTGA | 17970 |
| rs254052437 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799721 | CAGAAAAGAGGAGGG[A/G]GCATGGATGCTTCAC | 17970 |
| rs254064581 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152834552 | GAGATAGATCTTCAG[C/T]GTTTGTGCTATGGAA | 17970 |
| rs254086843 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152833590 | TGTTTATTAATATAC[A/T]GTTGTCTACTGATTT | 17970 |
| rs254101713 | snp | A/G | | | synonymous-codon | Ncf2 | Mm_Celera | 1:152834177 | GTGGTGTGAGCATAC[A/G]GTGGTGAGTGGAGGG | 17970 |
| rs254145534 | in-del | -/ACAG | | | utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152837055 | AGCTGCAGATCTTGC[-/ACAG]ACAGACAGACAGACA | 17970 |
| rs254212272 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152821699 | CCACTTGTTTCCCAG[A/G]ACACCATGATGGGGA | 17970 |
| rs254233591 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152818961 | aaaaaacaaaaaaaa[A/G]GAgaaagttattata | 17970 |
| rs254292203 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815532 | AGCCAAGAGCCTGCC[A/T]GCTCTGGGGGTGTGG | 17970 |
| rs254302966 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822069 | TTCTTTATTTGGAGA[C/T]GTTTCATTCAAAATT | 17970 |
| rs254337331 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152828908 | TTAGAGAGAGGGAGG[A/G]ACAGGGTGATGGGAC | 17970 |
| rs254354532 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152809545 | AGATGACACCACCCA[A/C]AAGGGCCTTTCCCCC | 17970 |
| rs254388234 | snp | C/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798521 | AACGTTTGCTTTAAA[C/T]TTGACTCAAAATTGT | 17970 |
| rs254404604 | in-del | -/GCAGA | | | intron-variant | Ncf2 | Mm_Celera | 1:152832093 | GAGTTGCACATGTCT[-/GCAGA]GCAGAGCCCCCAGGG | 17970 |
| rs254408090 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152800591 | TCTGACACCATGATT[C/T]ATCCACCATCATGGA | 17970 |
| rs254429773 | in-del | -/CA | | | intron-variant | Ncf2 | Mm_Celera | 1:152832721 | TCTGCCTACAGAGTG[-/CA]CACTTCTCATCCAGA | 17970 |
| rs254483066 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814186 | ATTTCTCCAACCACC[A/G]TGCTTGGCCTTTGTT | 17970 |
| rs254542284 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804911 | AGAACTTGAACAGAA[C/T]TTGGGTTCTGTCATA | 17970 |
| rs254591461 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809196 | CTCTGAGATTGCACA[A/G]CAAGTGCCTTTGTCT | 17970 |
| rs254601063 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152828100 | GAACAAAGCAAGCCA[C/T]CTTCCTCCTCCAATA | 17970 |
| rs254603921 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814731 | AATTCCATTCAAACT[A/C]TCACACCCATATGTG | 17970 |
| rs254615945 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152827630 | CCAGTGGGCGTGGTC[A/G]CCTTACAATGGGAGG | 17970 |
| rs254617753 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152821440 | CAGTCAGCATTCCCT[A/G]TGTGTACATGTGAAC | 17970 |
| rs254653976 | in-del | -/AA | | | intron-variant | Ncf2 | Mm_Celera | 1:152819962 | TACTATAGTTAAGTT[-/AA]AAAAAAAAAATCTTG | 17970 |
| rs254723311 | in-del | -/G | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152807984 | ACCCGGCAGCTCTGA[-/G]GAGAGACACCTTGAA | 17970 |
| rs254770962 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804583 | ACACGTGCATCAGTG[G/T]TTTTTTTTTTTCTTT | 17970 |
| rs254843156 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152809376 | CGGCTTACACTTCCA[C/T]CCTGCTGTTCATCAC | 17970 |
| rs254858850 | in-del | -/TTTTTTTTTTTTTTT | | | intron-variant | Ncf2 | Mm_Celera | 1:152817413 | TACCTGAGAGGAAAC[-/TTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 17970 |
| rs254890237 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152820234 | AAAGGGAAGCGAGAG[C/T]TTTGTTCTGGGGTTG | 17970 |
| rs254951439 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152827010 | GTCGGCACTCTTAAC[C/G]GCTGAGCCATCTCAC | 17970 |
| rs255049436 | in-del | -/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152825246 | CTTCACTGAATTAGG[-/C]GGAAAAGCATCTGAG | 17970 |
| rs255109821 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152823392 | ATCTGCACATAACTC[A/G]CAGCATCTGTGGTTG | 17970 |
| rs255155562 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152801742 | CCAAATAAAACAGCA[A/G]TCATGATTTTAAAGG | 17970 |
| rs255199958 | in-del | -/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813870 | TCAGCCTCAGGAGGA[-/G]GGAAGTGGCCAAATA | 17970 |
| rs255204600 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802819 | TAATAGTTTTTATGT[C/T]CCAAGTTAGCATGGG | 17970 |
| rs255222647 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818330 | CATGATCAAAATGGT[C/T]CCCAAACTGTCACTC | 17970 |
| rs255267825 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152837374 | CTGAATGCAGAGCTT[A/G]CATACACAAACTGGG | 17970 |
| rs255271722 | snp | C/G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152816584 | CAGCTATAGCTGTAA[C/G/T]GAGGAACCCCTGGCA | 17970 |
| rs255281547 | in-del | -/ACACACACACACACACAC | | | intron-variant | Ncf2 | Mm_Celera | 1:152825348 | CACACACACACACAT[-/ACACACACACACACACAC]ACACACACACACACA | 17970 |
| rs255292441 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802028 | TCTCTGGCCTTTAAC[C/T]CTCTCTTGTTCTTCT | 17970 |
| rs255389002 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152825716 | ATTTAACTAAAAGAG[A/G]GGGTGAGAGTAAGAT | 17970 |
| rs255410955 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152817310 | CATTGACAAAGGGAG[A/G]AAAGAAAGGGAGAGG | 17970 |
| rs255445043 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152815753 | GGGGGGGGGGTGAGG[-/A]GGGAAGCCAGGCAAA | 17970 |
| rs255479668 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152824637 | AGAGGGCCAGCAGGA[-/G]ATGCCCTTGGCTCAA | 17970 |
| rs255479893 | snp | A/G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152801278 | TACTTAGGTTGTGGC[A/G/T]AATTCAAGCCAGACC | 17970 |
| rs255623499 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825771 | CCTCCAAAAGCTACC[C/T]GAGTGACAATGGCTT | 17970 |
| rs255670203 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152816420 | TGTGCTTACAGACAG[A/G]GGTCCAGGAAGCCTA | 17970 |
| rs255729144 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152831311 | TGCTGAGTCACAGAA[C/T]TGAGGTGCTTTGAAG | 17970 |
| rs255798901 | snp | G/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799552 | CCCAAGTGCTGGGAT[G/T]AAAGGCATGCACAAC | 17970 |
| rs255800639 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152811283 | CAGCCCTCTCAACAA[C/T]GTCCTTAATGAGGAC | 17970 |
| rs255939060 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152805627 | TGCTTTAAAGCTTAT[G/T]ATAAATATAGGGTTT | 17970 |
| rs255962000 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806736 | GTTGAGAGGAAATTC[A/G]GTCATTATTTCGGAG | 17970 |
| rs255987325 | snp | C/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799964 | CACAGAGCCTCCTAT[C/T]AGGCATACCCTGCCT | 17970 |
| rs256002146 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804971 | AGGTCGTCGGCTAGC[A/T]GTGGGGAGTATTGAT | 17970 |
| rs256026403 | snp | C/T | | | synonymous-codon | Ncf2 | Mm_Celera | 1:152835032 | ACCATTTCAGGGTGA[C/T]CAAGGTCTTATTGAT | 17970 |
| rs256038705 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802431 | ATTGATCACATGGTG[G/T]Tttttgttttgtttt | 17970 |
| rs256165818 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152829859 | GTCCTGGAACTCTCT[C/T]TGTAGACCAGGCTGG | 17970 |
| rs256183030 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152810735 | AAACAAGGAGGTTCA[A/C]GAAGATTAGGTAATT | 17970 |
| rs256195091 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152810150 | CAAACGGAGGCAGCT[A/C]TCCCAGACAAGGCTC | 17970 |
| rs256236728 | snp | C/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799643 | CCATTGTATTCCAAC[C/T]GGCTGGGAGTGTTTC | 17970 |
| rs256251702 | in-del | -/CCTCA | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799619 | ACTTCACAGGCCTTG[-/CCTCA]CTGTGTGTCCATTGT | 17970 |
| rs256259391 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152821053 | TGCTATGTCACTGTC[C/T]GGCTATTCATGGCAT | 17970 |
| rs256271642 | snp | A/C | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798703 | TGCCATTAATCTCAG[A/C]AGTCAGGAGGCAGAT | 17970 |
| rs256280141 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152823841 | GGATCTGGTAGGAGT[C/T]AAGAGGAGGAGTTAG | 17970 |
| rs256339377 | snp | G/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798282 | TCCTGAAATGACGGA[G/T]GCTATTGTTTATGGA | 17970 |
| rs256344835 | in-del | -/GAGT | | | intron-variant | Ncf2 | Mm_Celera | 1:152830253 | TAAGATGTGGAATTA[-/GAGT]GAGTGCCAAGCTAAG | 17970 |
| rs256380965 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152805754 | AGAGCTTCACAAATG[C/T]GGTATGACCCATTTG | 17970 |
| rs256405451 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152803844 | ATGATGCAACCCCCA[C/G]CCTCAGAAAGAACTT | 17970 |
| rs256451454 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804283 | GTTTTATAAGGTTTC[-/T]TTTTAAGATAAATAA | 17970 |
| rs256525477 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813491 | TTTTTTTCTTTTTCC[A/T]TTTAAGATTATTTTA | 17970 |
| rs256533338 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812871 | AGTTGCAGACCTAAA[G/T]ATTAATTTTGGTGGA | 17970 |
| rs256588180 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808703 | GGGCATTTCAGCATC[-/T]TTTTTTGTTTTTTGT | 17970 |
| rs256604961 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152828708 | ACCCCCCTTGTCTGA[A/G]AAACAAGCAAAGAAA | 17970 |
| rs256644622 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826900 | CACTGTAGCTGTCTT[C/T]AGATACTCCAGAAGA | 17970 |
| rs256729435 | in-del | -/ACTCTA | | | intron-variant | Ncf2 | Mm_Celera | 1:152806625 | CCGCCATCAGGCTAG[-/ACTCTA]ACTCCTTCAATCATT | 17970 |
| rs256787644 | in-del | -/TC | | | intron-variant | Ncf2 | Mm_Celera | 1:152829602 | ACGTTTCTTTTTTTT[-/TC]TTTTCTTTTTAATAA | 17970 |
| rs256805358 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152832252 | ACAGAGTCATCCTGC[G/T]CACGACCACCTGATG | 17970 |
| rs256856777 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152819669 | ACCAGCTACTTAGTC[A/G]TGCTGAACTAAACTG | 17970 |
| rs256890223 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152834317 | AGTTATAGAGGACTT[C/T]GGATGAGTGGGACCC | 17970 |
| rs256894770 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814696 | AGTCATATTCTCTAT[G/T]TGTATGGTCTATGGG | 17970 |
| rs256945219 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802505 | CTCTGTATAGCCCTG[G/T]CTGTCCTGGAGCTCA | 17970 |
| rs257003302 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152828359 | ATGGGAGACTCTCTC[C/T]AGGAGTGGAGAAGTA | 17970 |
| rs257008557 | snp | A/G | | | utr-variant-5-prime, intron-variant | Ncf2 | Mm_Celera | 1:152807652 | AAGAGTCAAGTACAG[A/G]ACCAGGCCCAGACCT | 17970 |
| rs257054962 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152826511 | GGAAAGGACCTTGGA[A/C]CTCGTCACCTTCTTG | 17970 |
| rs257148876 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809670 | AAGCTGACACACAAA[A/G]CCAGCCAGTACAGTC | 17970 |
| rs257161389 | in-del | -/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152810812 | TCCAAGATCTCTGTA[-/C]CCCGGGGCCAGTTTT | 17970 |
| rs257199102 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818360 | CACCCTGCCGAGGGC[C/T]GCTTGTCACTTACAG | 17970 |
| rs257201789 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152819984 | AAAATCTTGAGTCCA[A/G]ATCCTGAGTCCTTGG | 17970 |
| rs257259828 | in-del | -/ACACACACAC | | | intron-variant | Ncf2 | Mm_Celera | 1:152811810 | CACACACAAACACAT[-/ACACACACAC]ACACACACACACACA | 17970 |
| rs257312780 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813509 | TAAGATTATTTTACA[A/T]ATGGAAGGACCAGAG | 17970 |
| rs257365177 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802596 | GGGATTAAAGGTGTG[C/T]GCCACCACGCCCGGC | 17970 |
| rs257405852 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814281 | CTTACATAGGGTTTC[A/G]TTGCTGTGAAGAAAC | 17970 |
| rs257405973 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826084 | TGGCTGGTTGGGAGC[C/T]GGCCCTGTCAGCTCT | 17970 |
| rs257430143 | in-del | -/GGGGT | | | intron-variant | Ncf2 | Mm_Celera | 1:152830499 | CAATGGACAGGTATG[-/GGGGT]GGGGTGGGGTGGGGT | 17970 |
| rs257442768 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152825048 | CATGGCCAAGTGCTG[A/G]AGATAGCTCAGTTGT | 17970 |
| rs257474884 | in-del | -/CAG | | | intron-variant | Ncf2 | Mm_Celera | 1:152831976 | GCCAGTGGCCATCAT[-/CAG]AGCAGTCACCAGGTG | 17970 |
| rs257500543 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152810509 | TTTTGACAACATGTG[C/T]GTACCTGATTCTCAA | 17970 |
| rs257530084 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152806330 | GAAGAGGAGGAAGAT[A/C]ACAACATTGCTTATA | 17970 |
| rs257557788 | in-del | -/GTTT | | | intron-variant | Ncf2 | Mm_Celera | 1:152809808 | TTTGTTTTGGTTTTG[-/GTTT]GTTTGTTTGTTTGTT | 17970 |
| rs257676425 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152802043 | CTCTCTTGTTCTTCT[-/G]GGGCCAACAGCTGAT | 17970 |
| rs257903051 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152828183 | TCCCAAAGAGAAGGG[C/T]TTGAAGGAGCTCATT | 17970 |
| rs257905687 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152828896 | GGAGAAGGAAGGTTA[A/G]AGAGAGGGAGGGACA | 17970 |
| rs257959969 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152831955 | TGAGTGCAGGTAATG[G/T]GGCCCGCCAGTGGCC | 17970 |
| rs257979041 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152834923 | TCAGTATTCATAGAA[C/T]GTGTTAGGCCTATAA | 17970 |
| rs258053933 | in-del | -/TC | | | intron-variant | Ncf2 | Mm_Celera | 1:152819283 | CTTCCTTCCTTTCTT[-/TC]TTTCTTTCTTTCTTT | 17970 |
| rs258163318 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813837 | aaaggggggggcttt[A/G]atagctggaccctgg | 17970 |
| rs258164453 | snp | C/T | | | utr-variant-5-prime, intron-variant | Ncf2 | Mm_Celera | 1:152807506 | AAACAGTCAGTGTAG[C/T]GGCTGCACATCTATC | 17970 |
| rs258171188 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804696 | TCAAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 17970 |
| rs258207904 | snp | A/C | | | missense | Ncf2 | Mm_Celera | 1:152834089 | GGCGTCGGGACAGCC[A/C]CGAGCTTCTGCTCCT | 17970 |
| rs258239713 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813090 | CTCTTACTGGCTGAG[C/T]CATCTCACCAGCCCT | 17970 |
| rs258260833 | in-del | -/TC | | | intron-variant | Ncf2 | Mm_Celera | 1:152808562 | TTACGCAACATCCTA[-/TC]TCAGTTTGGCCTGCT | 17970 |
| rs258365674 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152828859 | GTAGCCGTCTGTCCA[C/T]ACAGGATCGGCTGTC | 17970 |
| rs258367737 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822465 | AAAGAGTCAGTGCTC[C/T]AGAAAAAGAGAGTGT | 17970 |
| rs258382634 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809426 | CCTCAAGCAGGTCAG[A/G]AAGCAGGAGCTGATG | 17970 |
| rs258397307 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152830317 | GGATATGGTCCAAGC[C/T]GAATGGTGGGCTCAG | 17970 |
| rs258403023 | in-del | -/CTTC | | | intron-variant | Ncf2 | Mm_Celera | 1:152833756 | AGCCGCTAAGGTGGT[-/CTTC]CTTCCTTCCTCCTGC | 17970 |
| rs258500685 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152815842 | GCTTGCAAGAAGCAA[A/G]CTTAGCTCACTTGAT | 17970 |
| rs258513411 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822146 | CATCCAGAAGGGTGA[C/T]GGATCCTCTGGAGCT | 17970 |
| rs258514128 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152822964 | TTGGATTTAAGGCCC[A/G]CTGCATAGGAGGAAA | 17970 |
| rs258627909 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827085 | TTAAATATCCAGAAA[C/T]GTCACATATTGTGGC | 17970 |
| rs258642413 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152805015 | CCTGCTCTGAGAACA[C/T]CATTACGAGCTGACC | 17970 |
| rs258647206 | in-del | -/CAGCT | | | intron-variant | Ncf2 | Mm_Celera | 1:152816964 | TGACCTGCATGGGAC[-/CAGCT]CTCTTCTCCTCCTGT | 17970 |
| rs258663591 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152820041 | GAGATGCTTGTGGCT[-/A]AAGGCCGATGACCTT | 17970 |
| rs258689899 | in-del | -/TTTTT | | | intron-variant | Ncf2 | Mm_Celera | 1:152822565 | AAATAGTCTGTATTG[-/TTTTT]TTTTTTTTTTTTTGC | 17970 |
| rs258703970 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152828273 | AACGAGGGCAGGGCT[A/G]AGCAGAACGAACATC | 17970 |
| rs258742572 | snp | A/C | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799565 | ATTAAAGGCATGCAC[A/C]ACTACTGCCAGGCTT | 17970 |
| rs258754783 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152816026 | TACGTTAGCAGAGCT[A/G]CCCCATCCACCAGCT | 17970 |
| rs258788030 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814304 | GAAGAAACACTATGA[C/T]CAAATCAACTATTTA | 17970 |
| rs258847477 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152803975 | GTAGAGAATCTTGGG[A/G]ACATTTGGAAAGGCA | 17970 |
| rs258867319 | in-del | -/AACTTGG | | | intron-variant | Ncf2 | Mm_Celera | 1:152805842 | CCAGAAGACTATGTT[-/AACTTGG]AACTGATGGTATTTC | 17970 |
| rs258882112 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152832640 | CCCCTGAGAGCCACT[G/T]AAATATAAGTTAGAG | 17970 |
| rs258888303 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809235 | CGATCTCACAGCTCC[A/G]CGGGAGCTTCACCTG | 17970 |
| rs258902534 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152803371 | GCAGTCATGCAGAAT[A/G]GTGGGCCATCTGCAG | 17970 |
| rs258929099 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827770 | TCTTTCCTGTGTGCG[-/T]TTTTTCTAAAGCAGG | 17970 |
| rs258968857 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813918 | GCTAGCTTTAGGAAC[G/T]GAACCCAAGGGTTTT | 17970 |
| rs259004933 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152809591 | GAAAATGCCTTACAG[C/T]TGGATCTCATGGAGG | 17970 |
| rs259036373 | snp | A/G | | | synonymous-codon | Ncf2 | Mm_Celera | 1:152835092 | CAGTAAGCAGACTAC[A/G]GAGCCTCAGCCTAAG | 17970 |
| rs259188969 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827305 | GTCTTTGTTTTTGGA[-/T]CTGGAACAGTATTCC | 17970 |
| rs259214208 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814916 | TATTGAATGGGTTAG[G/T]CATTCCTTTCCATTG | 17970 |
| rs259388296 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812338 | CTGAGTGCTTTGATA[A/G]AGGGTGGCGCCTTAA | 17970 |
| rs259499745 | in-del | -/CT | | | intron-variant | Ncf2 | Mm_Celera | 1:152821281 | TTGTCCCCTCCTGAC[-/CT]CTACTTGGTTGTTGA | 17970 |
| rs259528783 | in-del | -/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798505 | CTGGCCAGTATTTAA[-/T]AACGTTTGCTTTAAA | 17970 |
| rs259563390 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152824755 | TTCTGAACACAGGTC[A/T]TAAGTTCTTTCAGAC | 17970 |
| rs259570416 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152815977 | TGGATACATCAGACC[C/G]TATTTCAACATAACA | 17970 |
| rs259575467 | snp | C/T | | | synonymous-codon | Ncf2 | Mm_Celera | 1:152817067 | ATAGACTACAAGATC[C/T]TGGGGCTGCAGTTCA | 17970 |
| rs259685484 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152818334 | ATCAAAATGGTCCCC[A/G]AACTGTCACTCACCC | 17970 |
| rs259692481 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152817978 | GTCTTCTTTTGCTTC[A/G]GTTTCTCAGGCACGA | 17970 |
| rs259697324 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825242 | CCTGCTTCACTGAAT[C/T]AGGCGGAAAAGCATC | 17970 |
| rs259700635 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152801881 | TTTTCCCTGTCCAAT[C/T]ACAGGCTTCTTGTTG | 17970 |
| rs259706394 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825632 | ATACCACAGAAATGT[C/T]CACTTAAAATGGTCA | 17970 |
| rs259739197 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152800529 | GTGAGTATGAGTTGG[C/T]CCCCTGCATCCTGAC | 17970 |
| rs259774538 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152801230 | CTGAGGACAGGCAGG[G/T]GGGCTCTGGTTGCAC | 17970 |
| rs259839356 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152800601 | TGATTTATCCACCAT[C/G]ATGGACTGTACCCTG | 17970 |
| rs259849742 | snp | G/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152836497 | TTGGGTTCCAGAAGC[G/T]TAAAGCAAATTTATA | 17970 |
| rs259854271 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826058 | ATCCCTACTCTCAGC[C/T]CTAGTTTACATGGCT | 17970 |
| rs259878091 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152823736 | TGGTCTACATCGTGA[A/G]CTCTAAACCAGCTAA | 17970 |
| rs259882312 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820763 | ATCTCTGGGCTGGTA[C/G]TCTTGGGTTCTATAA | 17970 |
| rs259933462 | in-del | -/TC | | | intron-variant | Ncf2 | Mm_Celera | 1:152827349 | CAGTCTGTTCTCTCT[-/TC]CCCCCCCGCCCCCTC | 17970 |
| rs259965463 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152803947 | TTAAGATGTTTTTGT[G/T]AGTGATTCTGATGTA | 17970 |
| rs259978515 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825970 | TCTCTGGGAAGTAGA[C/T]CCCGATAAGAGGAGC | 17970 |
| rs260003031 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152823228 | CAGAGAATCAATGGC[C/T]GAGTAGTGCTCAGAT | 17970 |
| rs260022587 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152834837 | CCTGGGTCTGTGTAA[A/G]GTTTATTATGTAAGG | 17970 |
| rs260056032 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152811058 | GCCTGATGGATCGGG[C/G]TTTCTTCTGTAGTCT | 17970 |
| rs260056808 | snp | A/G | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800173 | AGCACTCTCCCGGAG[A/G]TCCCTGACTCTGGCT | 17970 |
| rs260056838 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806142 | GAGCTAGCTCTGAAG[A/G]CTAGGTTGGGTAAGT | 17970 |
| rs260078584 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814839 | GTCTGTGACTGTGGT[A/G]TAAAGCAAAGTTGGG | 17970 |
| rs260112896 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798199 | ACACAGAGAAACCTT[A/G]TCTCGAAAACCAAAA | 17970 |
| rs260115847 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152811368 | GAAAGCGAATCAATC[C/T]TGGCTTCACCCATGC | 17970 |
| rs260120255 | in-del | -/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152803520 | GCATTTATGCCTGAA[-/C]CAATTAGAACACTTG | 17970 |
| rs260140403 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152805487 | TGAATTATGAAACCA[C/T]GGCCATGAAGGCTGG | 17970 |
| rs260199137 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152810032 | TCAGCAAGCAGATGG[C/T]GCAGAGCACGGCCCC | 17970 |
| rs260238139 | in-del | -/TTTTTGTTTC | | | intron-variant | Ncf2 | Mm_Celera | 1:152822044 | AAGAGTGTTTTTTTT[-/TTTTTGTTTC]TTCTTTATTTGGAGA | 17970 |
| rs260239292 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806654 | AATCATTTCTTAAGA[A/G]TCAGTGTCAAGGATC | 17970 |
| rs260251534 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152812046 | GGGGGATACCCTGAA[A/G]GGGGAGGGGAATTGA | 17970 |
| rs260265113 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815728 | CTGAGGTCACAAGCG[C/T]GGGGGGGGGGGGGGG | 17970 |
| rs260294623 | in-del | -/TTG | | | intron-variant | Ncf2 | Mm_Celera | 1:152802459 | TTGTTTTGTTTTGTT[-/TTG]TTTTGGTTTTGGTTT | 17970 |
| rs260308027 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152829673 | AGACACACATCAGAT[C/T]CCATTACAGATGGTT | 17970 |
| rs260309486 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152833406 | GTCTAGCATGAGATA[G/T]CTCTTAGAATATGGA | 17970 |
| rs260387392 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813849 | TTTAATAGCTGGACC[C/T]TGGTAGTCAGCCTCA | 17970 |
| rs260429203 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809752 | CTCTGCCTCCCCAGC[A/G]CTAAGATTAGAAAGG | 17970 |
| rs260437479 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152821346 | AGTGTTTTCTTAACA[C/T]CGCTTATGTCTGATA | 17970 |
| rs260485075 | in-del | -/CGGCAT | | | intron-variant | Ncf2 | Mm_Celera | 1:152817258 | AAAAAGTGTTTTCCC[-/CGGCAT]GGCATGCTTGAGGCC | 17970 |
| rs260556915 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152816254 | TGTACTGTTAGTGCT[-/G]ATGACACTTAAAGTG | 17970 |
| rs260560029 | in-del | -/GCA | | | intron-variant | Ncf2 | Mm_Celera | 1:152825848 | GGCAAACAGAGCCTG[-/GCA]GCAGCAGCACGCTCA | 17970 |
| rs260563694 | in-del | -/CTCGC | | | intron-variant | Ncf2 | Mm_Celera | 1:152830180 | CACTCACATGGTGTT[-/CTCGC]CTTGTCTTCTCGGGG | 17970 |
| rs260655498 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152800972 | TAAGATGTGTGGGGC[G/T]TGACACCATTTTATT | 17970 |
| rs260675707 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152827244 | GGGCGGCAGGCTTTT[A/G]GTTTCCCAAATTGTG | 17970 |
| rs260695834 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152805748 | CTGGAAAGAGCTTCA[A/C]AAATGCGGTATGACC | 17970 |
| rs260703865 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814595 | GCAGGAGGTGACTGA[A/G]CCACTGGGCATGTCT | 17970 |
| rs260714051 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152820531 | GCCTGGGATGTTCAG[C/T]CACCCCCTTCCCTGG | 17970 |
| rs260773590 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152821225 | TCCCCAGGGGGCCCC[A/G]GGGAAGCTCTTCTTT | 17970 |
| rs260873709 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152802430 | AATTGATCACATGGT[-/G]GTTTTTGTTTTGTTT | 17970 |
| rs260879093 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152803223 | CTCCATATTTATTCT[A/G]CAAGAGAGCTTCCCA | 17970 |
| rs260888323 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152824931 | TGAATGGATATATGC[A/C]GTGTGATATGTCCAT | 17970 |
| rs260923456 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826885 | TATTATTTGTAAGTA[C/T]ACTGTAGCTGTCTTC | 17970 |
| rs261001763 | in-del | -/TC | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800283 | TTTCTTTTCTTTCTT[-/TC]TTTCTTTTTTTTTTT | 17970 |
| rs261028449 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816923 | CAGGAGGGCTTCTTG[A/T]CGTGGGCTCTGCATT | 17970 |
| rs261037701 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152823420 | TTGCCTGTAGAGGAT[C/T]AAGTCAGCCAACCTT | 17970 |
| rs261087188 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152802766 | CTGAATAAATAGTCA[C/T]TATTTTATGGTTCTA | 17970 |
| rs261145794 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152805257 | ATGCTCACTACTAGC[C/T]CTGGTTGCCTAGGGA | 17970 |
| rs261253656 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819567 | GCTTTATTGTGCACA[C/T]AGGACTAAGTTTCCA | 17970 |
| rs261304102 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152833964 | GCTGGGGATGCAGCA[-/G]GGGGTGGATGATGGG | 17970 |
| rs261389197 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152801414 | TAAAGTACTTGCACA[A/G]CATGTGAGAGGCTCT | 17970 |
| rs261414149 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152803781 | TATCATTGGCACTTA[C/G]AATAACAGTGATTGA | 17970 |
| rs261446328 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152800572 | GTGACCAGCTGCTTC[A/G]GGGTCTGACACCATG | 17970 |
| rs261520733 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152821879 | GGGATGTGCAGCCTA[C/T]AAACACGGTGAAGAC | 17970 |
| rs261531816 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152827902 | TTTAATCCCAGCACT[A/C]GGGAGGCAGAGGCAG | 17970 |
| rs261621615 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152805119 | GCAGCAGGGCTGGGT[G/T]GAGGACTGGAGCAGA | 17970 |
| rs261647004 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798678 | GGTTACTTATTTGCT[A/G]GGTGGCACATGCCAT | 17970 |
| rs261651686 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822991 | GAAACACATGCAGGT[A/T]CTGCAGAACTGAGCA | 17970 |
| rs261749496 | snp | A/G | | | synonymous-codon | Ncf2 | Mm_Celera | 1:152821590 | GCAGTTGGCATTGGC[A/G]ACCAACATGAAGTCC | 17970 |
| rs261776433 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808669 | ATTAAGTCATGAAGT[C/T]CACCAAGGGTATGGG | 17970 |
| rs261788453 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815503 | GACAGAAACGCCAAG[G/T]AAAAGTACTCTGGAG | 17970 |
| rs261810377 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152826007 | GACAAACTGATCACA[A/G]GGGTTCAGCCGCCTC | 17970 |
| rs261837023 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798418 | TCAGGATGGTTGCTC[A/G]CCCCTGATTGGATCT | 17970 |
| rs261872555 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814975 | CCTACCAAGGAGGGT[C/T]TGTCCCCTCGACCAG | 17970 |
| rs261990507 | snp | C/T | | | synonymous-codon | Ncf2 | Mm_Celera | 1:152831661 | ACCTCCTAATTCTAG[C/T]CCCCCAGGAAGACTC | 17970 |
| rs262020030 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820094 | CAGTAGAAGGAAAGG[A/G]CTGACCCCTACAAGT | 17970 |
| rs262053483 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826740 | CAGGCTCAGCCCAGC[A/T]AGAGGACAAGGAAGG | 17970 |
| rs262099939 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808240 | TAATTATAGCCTTTC[C/T]GCCTCTGGAAACCTC | 17970 |
| rs262158499 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152802613 | CCACCACGCCCGGCT[A/G]ATCACATGGTTTTTA | 17970 |
| rs262217138 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152824431 | GACACGCCCCCTCTC[C/T]CTGCCCTGTGGCATT | 17970 |
| rs262295162 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806060 | GGTGACTGCTGGACT[G/T]GGGAAAGAAGACGAG | 17970 |
| rs262346541 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825577 | AAATGTCTTGGCACC[A/T]GATAACATGTAGCAT | 17970 |
| rs262376318 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152830923 | GTCGAGTGGAGGCAA[A/C]AGTTATTCTACTGGA | 17970 |
| rs262408996 | in-del | -/CGGGGCTC | | | intron-variant | Ncf2 | Mm_Celera | 1:152830526 | GTGGGGTGGGTGGTT[-/CGGGGCTC]CGGGGAGATGCTAAG | 17970 |
| rs262430741 | in-del | -/AA | | | intron-variant | Ncf2 | Mm_Celera | 1:152833607 | TGTCTACTGATTTTT[-/AA]TAACTTATTAGATTT | 17970 |
| rs262474383 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152834630 | AGTAGGAATAGCCAT[G/T]TGCTGTCTGGCCTGA | 17970 |
| rs262496710 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152823635 | ATTTAAAATAAAAAA[A/G]GTTGGATACTGTAGG | 17970 |
| rs262497208 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809855 | CTCTGTAGGCTGTGA[A/G]GCTTGTGAGGCCAGC | 17970 |
| rs262551496 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152828607 | CCTCCTTAGAGGAGA[A/G]AGGAGGATAAGAGTT | 17970 |
| rs262629587 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152809949 | ATCCTCTGACCAGCC[A/T]GTGAAAAAACACATC | 17970 |
| rs262655105 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152829624 | TTTTAATAATTATTT[A/G]TTTTTTGTATGTGAC | 17970 |
| rs262689995 | in-del | -/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812521 | GAGGGCAGAATGCTG[-/T]ATATATAGTAAACAA | 17970 |
| rs262746313 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152805451 | AGAAGGTGGAGAGAG[A/G]AGAAGACACCATAGA | 17970 |
| rs262860123 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152809712 | CAGATCTTGCACATT[A/C]GGTTCAGCTGGCTAG | 17970 |
| rs262892838 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152833072 | CCTGGTGCTTCTGCC[C/T]GGGGCCTGGGGTTAT | 17970 |
| rs262933576 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152809001 | CAAGTGCTGGGATCA[A/G]AGGTGTTCAACATGA | 17970 |
| rs262985994 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808397 | GGGCTCTGCTCTTTA[C/T]GAGATCTCCTTATTA | 17970 |
| rs263032179 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808825 | CCTCTGCCTCCCGAT[C/T]AGCATCTTTTTAAAA | 17970 |
| rs263060272 | in-del | -/GG | | | intron-variant | Ncf2 | Mm_Celera | 1:152817327 | AGAAAGGGAGAGGGT[-/GG]GTGGGGGGAGGAAAG | 17970 |
| rs263107948 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152833238 | TCCTCTAGATCCACC[C/T]TGGATGTTAAAGGGT | 17970 |
| rs263149847 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152830786 | TGCTGAGGCCTAGCC[C/T]GTTGCTCTCACCCTT | 17970 |
| rs263163201 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814139 | AACCGCAGTCTTCAG[C/T]GAGAGCAGATACCAC | 17970 |
| rs263288477 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152831811 | CCTTGCTTTACCTAG[C/T]ATGCTCCTTGTTTTA | 17970 |
| rs263327494 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812573 | AGAAAGAGAGAGAGA[A/G]AAAGAAAGAAAGGAA | 17970 |
| rs263367175 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152807248 | GAAATCCTAAATCTG[G/T]GTTTACAGAGACTAG | 17970 |
| rs263430827 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152811737 | AGTAAAAAGAAAAAC[C/T]AAATCAAACAAAACA | 17970 |
| rs263472291 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152817371 | AGGGAGATTTCATGA[C/T]TTCGCACTCCTTATA | 17970 |
| rs263484188 | in-del | -/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815153 | GGGAGCAGGGTATGT[-/G]GGGGGCGGGGGGAGG | 17970 |
| rs263501291 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152835633 | CTATTATAATGCATA[A/G]TTTTTACAAATGTAC | 17970 |
| rs263550398 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152830193 | TTCTCGCCTTGTCTT[A/C]TCGGGGTCCTGGGTG | 17970 |
| rs263590652 | in-del | -/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152825437 | GTACCATGAAAAACA[-/C]GGAAAAAAGGCACAT | 17970 |
| rs263637289 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152810585 | TGGTTGGGAGCCACT[A/G]TGTGGGTGCTGGGAA | 17970 |
| rs263704356 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152816094 | TTTCTAAAACAAAAC[-/A]AAAACAAAACATTGT | 17970 |
| rs263727698 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152811218 | TAAGTCATCATTAGC[A/G]CACAGCGGCAAGGAG | 17970 |
| rs263729230 | snp | A/C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816083 | TAACTTGTCCTTTTT[A/C/T]TAAAACAAAACAAAA | 17970 |
| rs263770842 | in-del | -/AAA | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813640 | AGGATAAGGGACAAG[-/AAA]AAAAAAAAAAGGAAC | 17970 |
| rs263779123 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799341 | AAAAACTGAGCTCGG[A/G]TGCTTCTCAGTCTCC | 17970 |
| rs263798608 | in-del | -/TTTT | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800288 | TTTTCTTTCTTTTTC[-/TTTT]TTTTTTTTCCCATTC | 17970 |
| rs263825019 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152816007 | AACATTAACAAATGG[G/T]CAATACGTTAGCAGA | 17970 |
| rs263851168 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152833673 | ACCCCCCTTTCCCTG[A/G]GGCACTCCTGGTGCC | 17970 |
| rs263855201 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152834018 | ACTGGCTATGGGATG[C/T]TTTTTGTGTTGATAC | 17970 |
| rs263865861 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152831022 | GGTATTCCCAAGCCC[G/T]CCTCTTCACCAGGGA | 17970 |
| rs263883143 | snp | A/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799074 | TCTTTGATTAACTAT[A/T]GATAGGAAGTAGCCA | 17970 |
| rs263925867 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152810749 | AAGAAGATTAGGTAA[C/T]TTACCACAGGCTATG | 17970 |
| rs263936030 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815159 | AGGGTATGTGGGGGG[C/T]GGGGGGAGGGAGTGG | 17970 |
| rs264014473 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152819783 | TCTCGCCTCCTACAG[A/T]GAGCCACTTGCTTTC | 17970 |
| rs264077256 | in-del | -/TA | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813118 | CTCAGATTTTTTTTT[-/TA]AAAAGATTTATTTAT | 17970 |
| rs264108734 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814900 | TAGAGAGGTGAGTTG[A/G]TATTGAATGGGTTAG | 17970 |
| rs264114404 | snp | A/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152820624 | GGTTTTGTGTCAACT[A/T]GACACAGGTTAGAGT | 17970 |
| rs264128352 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152822694 | CTCTGTGCAGGGTAG[C/T]TCCAACAAGACCACA | 17970 |
| rs264196502 | in-del | -/A | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814809 | AGGAAGGTGTAGATT[-/A]AAAGGGGGAACTAAG | 17970 |
| rs264234886 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152826271 | CTTTGACTTCCTTGG[C/T]GCTGTCCATTTGCTC | 17970 |
| rs264292444 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152802557 | CGAACTCAGAAATCC[A/G]CCTGCCTCTGCCTCC | 17970 |
| rs264350469 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152825203 | ACTACCCATAGTAGT[C/T]AGCTCGGAGTTTGAT | 17970 |
| rs264366744 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152820271 | GCTGccagcgccagc[A/G]ccagcaccagcacca | 17970 |
| rs264468973 | in-del | -/CG | | | intron-variant | Ncf2 | Mm_Celera | 1:152811858 | ACACACACATGTACA[-/CG]CACAGATATATCAAA | 17970 |
| rs264533722 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152817138 | CGAGGGAAGCACAAA[A/G]GTCTAGCTGTTGTGA | 17970 |
| rs264563720 | in-del | -/AAA | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152829103 | ATCAAATTTCATTTG[-/AAA]AAAAAAAAAATGCCA | 17970 |
| rs264568471 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152823697 | GGCTGTGACAGACAG[A/G]TCTCTGTGAACTGCA | 17970 |
| rs264697215 | in-del | -/TAATTAAT | | | utr-variant-3-prime | Ncf2 | Mm_Celera | 1:152836448 | AGTTCAGTGGAAAAA[-/TAATTAAT]TAATTAATAAAGGGT | 17970 |
| rs264710280 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152801988 | ACTGAGATGGAGCAC[G/T]GAGAGGCAGAGCAGA | 17970 |
| rs264790474 | snp | A/G | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798926 | TAGAAAAATAGGAGC[A/G]AGGGAGGGGGTGAGG | 17970 |
| rs264806203 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152804747 | CATGCGACACCACGC[C/T]CGGCTGTACATCAGT | 17970 |
| rs264820503 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152820602 | CTCTTTCTACCTTGT[A/C]CTGGCTGGTTTTGTG | 17970 |
| rs264867862 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152816264 | GTGCTGATGACACTT[A/G]AAGTGTCCCCTCTGA | 17970 |
| rs264901543 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827174 | CAATAAAACCTTCTC[C/T]AGACACCTGCTCTGG | 17970 |
| rs264946249 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152803088 | TTACAAAACTCTATT[G/T]GCAGCTTTTATTCTA | 17970 |
| rs265009003 | snp | C/T | | | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152807304 | GAGTCATGTCTTCAG[C/T]TTCTCACAGACAGAC | 17970 |
| rs265026633 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152830246 | TAGGCAGTAAGATGT[A/G]GAATTAGAGTGAGTG | 17970 |
| rs265099017 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152806196 | AGCTGGCAGCAGGAG[C/T]CAGCCAGTAGAAGCC | 17970 |
| rs265121929 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152800654 | CCCTGCCTTCATTAC[A/G]ATGTTTCTGTCGGAG | 17970 |
| rs265144946 | in-del | -/GCAC | | | intron-variant | Ncf2 | Mm_Celera | 1:152825854 | CAGAGCCTGGCAGCA[-/GCAC]GCACGCTCACCTTCT | 17970 |
| rs265261867 | snp | C/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152810060 | CCCCATCCAGCCTCC[C/G]CCTGGAGGGAGGAAT | 17970 |
| rs265306527 | in-del | -/TA | | | intron-variant | Ncf2 | Mm_Celera | 1:152826828 | GAGAGACTCTTTTTT[-/TA]CAAAATATTTATTTA | 17970 |
| rs265357684 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152805943 | GACAGAGAGTAGGTT[A/G]TCCCCACCCTCAACA | 17970 |
| rs265385262 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152827705 | CTGACTACAGTGCAC[C/T]CCCCTCCCGCTCAGT | 17970 |
| rs265406383 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152819886 | GTCAATAGTGTGGGG[-/A]GAAAAAAAATCAAAA | 17970 |
| rs265450387 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152809143 | CTGTGGAGTTCCCTC[C/T]TTCCATTTTGACCTG | 17970 |
| rs265487142 | in-del | -/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152827242 | TGGGCGGCAGGCTTT[-/C]TGGTTTCCCAAATTG | 17970 |
| rs265545825 | snp | G/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152832145 | TGGATGGTGTGGATG[G/T]AAGATCTTCCCAGAA | 17970 |
| rs265556550 | in-del | -/TTGTTGTTG | | | intron-variant | Ncf2 | Mm_Celera | 1:152809254 | AGCTTCACCTGCTTC[-/TTGTTGTTG]TTGTTGTTGTTGTTG | 17970 |
| rs265586319 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152806682 | ATCTGAGACTTAAAG[A/G]CACTGTCCCAAATTT | 17970 |
| rs265591505 | snp | G/T | | | synonymous-codon | Ncf2 | Mm_Celera | 1:152808103 | GAAGGACTGGAAGGG[G/T]GCCCTGGAGGCCTTC | 17970 |
| rs265638442 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152816859 | TCATACATAGTCTGT[-/A]AAAGTCTTTGCGCTC | 17970 |
| rs265670655 | snp | A/G | | | missense | Ncf2 | Mm_Celera | 1:152836071 | AGGCTTTTGTTGAAG[A/G]ATGTGCAGCCAAGAA | 17970 |
| rs265719779 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152829832 | ACAGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTCC | 17970 |
| rs265758527 | in-del | -/AGT | | | intron-variant | Ncf2 | Mm_Celera | 1:152824974 | CCACAAGAAGGATAA[-/AGT]ACTAATGCATGCTAC | 17970 |
| rs265811638 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152816319 | TGTGGAACACAGTGG[A/G]AATTGTATCTGCTCA | 17970 |
| rs265820051 | in-del | -/ATGACCC | | | intron-variant | Ncf2 | Mm_Celera | 1:152805758 | CTTCACAAATGCGGT[-/ATGACCC]ATTTGGGGTGGGCTT | 17970 |
| rs265841261 | in-del | -/ATGTTAGGTGCT | | | intron-variant | Ncf2 | Mm_Celera | 1:152801020 | CCATATTTACTCAGA[-/ATGTTAGGTGCT]AGGTTCTGTGGGAAA | 17970 |
| rs265877347 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152834294 | AGTTATAGCAGGCAT[C/T]AGATAGCAGTTATAG | 17970 |
| rs265900674 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815465 | AGCTTCAGAGGTTAC[C/T]AAGGGGTCCCTATGG | 17970 |
| rs265991153 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152823400 | ATAACTCGCAGCATC[C/T]GTGGTTGCCTGTAGA | 17970 |
| rs266012121 | snp | C/T | | | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152798353 | GTTGAGCCAACTACA[C/T]GAATGTGCTAGATGA | 17970 |
| rs266020342 | snp | A/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152832939 | AGCACAGAGGTTCTT[A/C]CATCCTCAGTAGTAA | 17970 |
| rs266034022 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152819887 | TCAATAGTGTGGGGG[-/A]AAAAAAAATCAAAAT | 17970 |
| rs266078424 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814095 | GGGCTATGGATGGAT[A/G]TGAGCCACCATGTGA | 17970 |
| rs266134962 | snp | A/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152818451 | GTCCTTCACAGGAAG[A/G]CGTTTTCCCTGTTGT | 17970 |
| rs266198655 | snp | C/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152818792 | TGCGCGCCTTTAATC[C/T]CAGCACTCGGGAGGC | 17970 |
| rs266221874 | in-del | -/G | | | intron-variant | Ncf2 | Mm_Celera | 1:152804796 | CTACATCCCCGACTT[-/G]GATTGGGGACAGACT | 17970 |
| rs386842840 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152832417 | TGGCTCCACAGTCAA[-/A]GACGCTTGCTGCACA | 17970 |
| rs386846398 | in-del | -/CCCAGAGCCTGAGA | | | utr-variant-5-prime, intron-variant | Ncf2 | Mm_Celera | 1:152807603 | ACCCAGAGCCTGAGA[-/CCCAGAGCCTGAGA]GGACCAGAGCTAGCA | 17970 |
| rs386866553 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152826876 | TTATTTATTTATTAT[A/T]TGTAAGTACACTGTA | 17970 |
| rs386919828 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152828206 | AGCTCATTCCCCAAT[-/T]CTCTAAACTAAAGAG | 17970 |
| rs386948536 | in-del | -/A | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812550 | AATAAAACTAAAAAA[-/A]GAAAAGAAGAAAGAG | 17970 |
| rs386965318 | in-del | -/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152817258 | AAAAAGTGTTTTCCC[-/C]GGCATGGCATGCTTG | 17970 |
| rs386971621 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152837561 | AAAAAAACAAAAAAA[A/C]AAAAAAAAAAAGAAA | 17970 |
| rs387008961 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152832505 | ACACCACAAAGGAGC[-/A]TGGCTTGCCTCCGTG | 17970 |
| rs387028351 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812678 | AAGGAAGGAAGGAAG[A/G]AAGGAAGGAAGGAAG | 17970 |
| rs387059809 | in-del | -/TTTTTTT | | | intron-variant | Ncf2 | Mm_Celera | 1:152822048 | TGTTTTTTTTTTTTT[-/TTTTTTT]GTTTCTTCTTTATTT | 17970 |
| rs387078205 | in-del | -/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813832 | AGCCAAAAGGGGGGG[-/G]CTTTAATAGCTGGAC | 17970 |
| rs387129883 | in-del | -/ATTTGATG | | | intron-variant | Ncf2 | Mm_Celera | 1:152825656 | ATGGTCAATTTGATG[-/ATTTGATG]TTGTATGACTACCAG | 17970 |
| rs387146311 | in-del | -/AAACAAAACAAAACAAAACAAAACA | | | intron-variant | Ncf2 | Mm_Celera | 1:152803458 | AAACAAAACAAAACA[-/AAACAAAACAAAACAAAACAAAACA]GCATAGCATAAAAAC | 17970 |
| rs387183041 | in-del | -/TGAGGCTCGAG | | | intron-variant | Ncf2 | Mm_Celera | 1:152827156 | AAGGGTTGAGTTGAG[-/TGAGGCTCGAG]GTCAATAAAACCTTC | 17970 |
| rs387234382 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812586 | GAAAAAGAAAGAAAG[A/G]AAGGAAGGAAGGAAG | 17970 |
| rs387238513 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152837588 | AAAAAAGAAAAAAAA[-/A]TCCAAATACCATGTC | 17970 |
| rs387252799 | in-del | -/AAAACAAGCAAA | | | intron-variant | Ncf2 | Mm_Celera | 1:152828708 | ACCCCCCTTGTCTGA[-/AAAACAAGCAAA]GAAACAACTCTAAGA | 17970 |
| rs387257798 | in-del | -/GACCCAT | | | intron-variant | Ncf2 | Mm_Celera | 1:152805760 | TCACAAATGCGGTAT[-/GACCCAT]TTGGGGTGGGCTTTA | 17970 |
| rs387300200 | in-del | -/C | | | intron-variant | Ncf2 | Mm_Celera | 1:152808243 | TATAGCCTTTCCGCC[-/C]TCTGGAAACCTCATC | 17970 |
| rs387326116 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152818851 | CCAGCCTGGTCTACA[A/G]AGTGAGTTCCAGGAC | 17970 |
| rs387335557 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152832209 | ACTCTTTGTTCCTGG[A/T]GAGCTTCAGCAGATG | 17970 |
| rs387345750 | in-del | -/TGCAGCCAGGTGGGAGGGGGCAGC | | | intron-variant | Ncf2 | Mm_Celera | 1:152815760 | GGTGAGGAGGGAAGC[-/TGCAGCCAGGTGGGAGGGGGCAGC]CAGGCAAATGATTCG | 17970 |
| rs387358245 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812642 | AAGGAAGGAAGGAAG[A/G]AAGGAAGAAAGAAAG | 17970 |
| rs387397400 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152818905 | CTGTCTCGAAAAAAA[-/A]CAAAAACAAAAACAA | 17970 |
| rs387417240 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152809553 | CCACCCACAAGGGCC[C/T]TTCCCCCTTGATCAC | 17970 |
| rs387457667 | in-del | -/TTTT | | | intron-variant | Ncf2 | Mm_Celera | 1:152822579 | GTTTTTTTTTTTTTT[-/TTTT]GCGGGGGGGGGGGGA | 17970 |
| rs387482790 | in-del | -/TGAAAATTTTTGCT | | | intron-variant | Ncf2 | Mm_Celera | 1:152804496 | TTGAAAATTTTTGCT[-/TGAAAATTTTTGCT]GGGATATATAAGCTG | 17970 |
| rs387485244 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152820289 | AGCACCAGCACCAGC[A/G]CCAGCTATTACCTCC | 17970 |
| rs387606864 | in-del | -/AA | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813651 | CAAGAAAAAAAAAAA[-/AA]GGAACAAGTGAAAGG | 17970 |
| rs387617717 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152829802 | CATTTCTTTTTTTTT[-/T]CTTTTTTTTCCAAGA | 17970 |
| rs387627080 | in-del | -/ACGC | | | intron-variant | Ncf2 | Mm_Celera | 1:152825860 | CTGGCAGCAGCACGC[-/ACGC]TCACCTTCTTGTCTG | 17970 |
| rs387643215 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152808709 | TTCAGCATCTTTTTT[-/T]GTTTTTTGTTTTGTT | 17970 |
| rs387660789 | in-del | -/T | | | intron-variant | Ncf2 | Mm_Celera | 1:152803412 | GTTTGCCCTGGTCTT[-/T]CCTAGATGACTTCTG | 17970 |
| rs387679286 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152827856 | TCTCAGCTAAAAAAA[-/A]TCCTTCTAGCCAGGC | 17970 |
| rs387687152 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152804591 | ATCAGTGTTTTTTTT[G/T]TTTCTTTTGGTTTGG | 17970 |
| rs387700097 | snp | A/G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152818873 | TTCCAGGACAGCCAG[A/G/T]GCTACACAGAGAAAC | 17970 |
| rs387720337 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812674 | AAGGAAGGAAGGAAG[A/G]AAGAAAGGAAGGAAG | 17970 |
| rs387741423 | in-del | -/A | | | intron-variant | Ncf2 | Mm_Celera | 1:152816862 | TACATAGTCTGTAAA[-/A]GTCTTTGCGCTCAGG | 17970 |
| rs387744088 | in-del | -/ACACACACACACACACAC | | | intron-variant | Ncf2 | Mm_Celera | 1:152825376 | CACACACACACACAC[-/ACACACACACACACACAC]GCATACACTCACTAC | 17970 |
| rs387749302 | in-del | -/TGGAACT | | | intron-variant | Ncf2 | Mm_Celera | 1:152805846 | AAGACTATGTTAACT[-/TGGAACT]GATGGTATTTCAGCC | 17970 |
| rs387767053 | in-del | -/TG | | | intron-variant | Ncf2 | Mm_Celera | 1:152819192 | CTGGTGACCTTTGTG[-/TG]CTTTGTGCCCAGACC | 17970 |
| rs387794367 | in-del | -/TT | | | intron-variant | Ncf2 | Mm_Celera | 1:152804604 | TTTTTCTTTTGGTTT[-/TT]GGTTTGGTTTTTCAA | 17970 |
| rs387794820 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152802501 | GTTTCTCTGTATAGC[C/T]CTGGCTGTCCTGGAG | 17970 |
| rs387821820 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812622 | GAGAAAGAAAGAAAG[A/G]AAGGAAGGAAGGAAG | 17970 |
| rs387852813 | in-del | -/TTATTTATTTATTTATTTATTT | | | intron-variant | Ncf2 | Mm_Celera | 1:152826837 | CTTTTTTCAAAATAT[-/TTATTTATTTATTTATTTATTT]ATTTATTTATTTATT | 17970 |
| rs387896163 | in-del | -/ACT | | | intron-variant | Ncf2 | Mm_Celera | 1:152832508 | CACAAAGGAGCATGG[-/ACT]CTTGCCTCCGTGCAT | 17970 |
| rs578320902 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152803539 | TTAGAACACTTGCCA[A/G]GATGTGGAAAGGAAC | 17970 |
| rs578333186 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814371 | CCAGAAGAGGGCATC[A/G]GATCCCATTACAGAT | 17970 |
| rs578352589 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152821858 | GGTAATATGTGCAGC[C/T]TCTCGGGGATGTGCA | 17970 |
| rs578360602 | snp | C/T | | | upstream-variant-2KB | Ncf2 | GRCm38.p3 | 1:152799444 | CTAAATTCTGATTCT[C/T]CCCCCCACCCCCCAA | 17970 |
| rs578414857 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152809518 | CTTATAGAACCAAGA[C/T]TACCAGCCCAGAGAT | 17970 |
| rs578430775 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152818870 | GAGTTCCAGGACAGC[C/T]AGGGCTACACAGAGA | 17970 |
| rs578435990 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152801478 | GGGTAGGCTGGGAGG[A/C]TGGATAACAGTAAAG | 17970 |
| rs578439382 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152828262 | GGGACTTTGCAAACG[A/T]GGGCAGGGCTGAGCA | 17970 |
| rs578808732 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152801470 | GTGGGGTGGGGTAGG[C/T]TGGGAGGATGGATAA | 17970 |
| rs578834815 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152818780 | CAGGCAAGGTGGTGC[A/G]CGCCTTTAATCTCAG | 17970 |
| rs578910913 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152809536 | CCAGCCCAGAGATGA[C/T]ACCACCCACAAGGGC | 17970 |
| rs578969037 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152818927 | CAAAAACAAAAAAAA[A/C]AAAAAACAAAACAAA | 17970 |
| rs579001560 | snp | C/T | | | upstream-variant-2KB | Ncf2 | GRCm38.p3 | 1:152798490 | GTCAGAGTCTATCAT[C/T]CTGGCCAGTATTTAA | 17970 |
| rs579005357 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813081 | CAGTCAGTGCTCTTA[A/C]TGGCTGAGCCATCTC | 17970 |
| rs579023430 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152825241 | CCCTGCTTCACTGAA[C/T]TAGGCGGAAAAGCAT | 17970 |
| rs579062872 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152804803 | CCCGACTTGGATTGG[A/G]GACAGACTGTCGGAG | 17970 |
| rs579418353 | snp | C/G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152804595 | GTGTTTTTTTTTTTT[C/G/T]TTTTGGTTTGGTTTG | 17970 |
| rs579440819 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152822745 | ACTGGTCACAGGACA[C/T]GGAGAAATCATGTTG | 17970 |
| rs579510415 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152816852 | GCAAAAGTCATACAT[A/C]GTCTGTAAAAGTCTT | 17970 |
| rs579536089 | snp | C/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152806962 | CCTCTTCTTCTTCCT[C/G]CTCCTCCTCCTCTTT | 17970 |
| rs579543692 | snp | A/G | | | upstream-variant-2KB | Ncf2 | GRCm38.p3 | 1:152799675 | GTCCAAATGTGGGCC[A/G]TGCTTTTGCTGTGGT | 17970 |
| rs579703186 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152831723 | GGAGCTCTCTCTCTC[A/T]GATGCTTCATGAAAA | 17970 |
| rs579713541 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152819261 | CAATCTTTAGAACCC[A/C]TCTTTCCTTCCTTCC | 17970 |
| rs579718095 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152819159 | AGAAGGCTGGGGTGG[A/G]TGTGACCCTTTAATC | 17970 |
| rs579726817 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152802479 | GGTTTTGGTTTTTCG[A/G]GACAGGGTTTCTCTG | 17970 |
| rs579751576 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152833267 | GTAGGGAGATGGGCA[C/T]TGTGGGTGGCAGGTG | 17970 |
| rs579938592 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152802467 | GTTTTGTTTTTTGGT[G/T]TTGGTTTTTCGAGAC | 17970 |
| rs580109178 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152802462 | GTTTTGTTTTGTTTT[G/T]TGGTTTTGGTTTTTC | 17970 |
| rs580219062 | snp | C/T | | | upstream-variant-2KB | Ncf2 | GRCm38.p3 | 1:152799450 | TCTGATTCTCCCCCC[C/T]ACCCCCCAAGACAGG | 17970 |
| rs580382500 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152827675 | CCCAGGTCAGAGGTG[A/G]GAGGTCAGTTTGTAC | 17970 |
| rs580394760 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152809169 | ACCTGGATCCAGTGA[C/T]CGACCCCAAATCTCT | 17970 |
| rs580516349 | snp | C/T | | | upstream-variant-2KB | Ncf2 | GRCm38.p3 | 1:152799447 | AATTCTGATTCTCCC[C/T]CCCACCCCCCAAGAC | 17970 |
| rs580555974 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815161 | GGTATGTGGGGGGCG[A/G]GGGGAGGGAGTGGGG | 17970 |
| rs580737720 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152809496 | ATTGGCTTGCTCAGC[C/T]TGCTCTCTTATAGAA | 17970 |
| rs580745314 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152834786 | TTTGTGGCTCAATAT[C/T]ATTTCCCAATCTGAA | 17970 |
| rs580765340 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152828026 | AAAAAACAAAAAAAA[A/C]AAAAAAAAGAAAAGA | 17970 |
| rs580816551 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152803068 | AAGCTCATGAACCTG[A/C]AGGTTTACAAAACTC | 17970 |
| rs580846423 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152804572 | TGTACATGTGCACAC[A/G]TGCATCAGTGTTTTT | 17970 |
| rs580872389 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152822568 | TAGTCTGTATTGTTT[G/T]TTTTTTTTTTTTTTG | 17970 |
| rs580891679 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152820796 | AAGCAGGCTGAGCAA[A/G]CCAGGGGAAGCAAGC | 17970 |
| rs581223917 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813002 | AAGAGCATCAGATCT[C/T]GTTACAGATGTTTGT | 17970 |
| rs581292829 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | GRCm38.p3 | 1:152836600 | CAGGTTCCCATGAAG[C/T]ACACCATCCAGTCCC | 17970 |
| rs581305983 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152827883 | AGGCGTGGTGGTGCA[C/T]GCCTTTAATCCCAGC | 17970 |
| rs581362960 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152809238 | TCTCACAGCTCCGCG[A/G]GAGCTTCACCTGCTT | 17970 |
| rs581390566 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152819872 | AGGGTTTTGCAGTGT[G/T]TCAATAGTGTGGGGG | 17970 |
| rs581410160 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152809530 | AGATTACCAGCCCAG[A/G]GATGACACCACCCAC | 17970 |
| rs581488265 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152817275 | GCATGGCATGCTTGA[G/T]GCCCAGGATCTGACA | 17970 |
| rs581491830 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152818777 | TGCCAGGCAAGGTGG[C/T]GCGCGCCTTTAATCT | 17970 |
| rs581560583 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152829045 | AAGGCCCAGGGCAGG[A/G]GGAGTAGGGTTTGAG | 17970 |
| rs581595077 | snp | A/G | | | utr-variant-5-prime | Ncf2 | GRCm38.p3 | 1:152800502 | CTCCCTGCATAAAGA[A/G]AAGAAGGCTACGTGA | 17970 |
| rs581769627 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152818796 | CGCCTTTAATCTCAG[A/C]ACTCGGGAGGCAGAG | 17970 |
| rs581886266 | snp | C/T | | | upstream-variant-2KB | Ncf2 | GRCm38.p3 | 1:152799445 | TAAATTCTGATTCTC[C/T]CCCCCACCCCCCAAG | 17970 |
| rs581892343 | snp | A/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152801471 | TGGGGTGGGGTAGGC[A/T]GGGAGGATGGATAAC | 17970 |
| rs581986995 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152814393 | ATTACAGATGGTTGT[A/G]AGCCACCATGTGGTT | 17970 |
| rs581996227 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152805827 | AATTAGCCAGGGATG[A/G]CCAGAAGACTATGTT | 17970 |
| rs582116675 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152825331 | TGTGCCCCCAGGCAT[A/C]ACACACACACACACA | 17970 |
| rs582177804 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813083 | GTCAGTGCTCTTACT[A/G]GCTGAGCCATCTCAC | 17970 |
| rs582186056 | snp | C/T | | | upstream-variant-2KB | Ncf2 | GRCm38.p3 | 1:152798508 | GGCCAGTATTTAAAA[C/T]GTTTGCTTTAAATTT | 17970 |
| rs582289971 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152831701 | CCAGGTTGGTGGCCC[C/T]GAGGAAGGAGCTCTC | 17970 |
| rs582483967 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152804783 | ATTATCACCAACCCT[A/G]CATCCCCGACTTGGA | 17970 |
| rs582594547 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152809537 | CAGCCCAGAGATGAC[A/C]CCACCCACAAGGGCC | 17970 |
| rs582657477 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152802464 | TTTGTTTTGTTTTTT[G/T]GTTTTGGTTTTTCGA | 17970 |
| rs582683608 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152818943 | AAAAAACAAAACAAA[A/C]CAAAAAAACAAAAAA | 17970 |
| rs582703440 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152832206 | ATGACTCTTTGTTCC[C/T]GGTGAGCTTCAGCAG | 17970 |
| rs582857462 | snp | C/T | | | upstream-variant-2KB | Ncf2 | GRCm38.p3 | 1:152799448 | ATTCTGATTCTCCCC[C/T]CCACCCCCCAAGACA | 17970 |
| rs583027215 | snp | A/T | | | utr-variant-5-prime | Ncf2 | GRCm38.p3 | 1:152800180 | TCCCGGAGGTCCCTG[A/T]CTCTGGCTGTGCTCT | 17970 |
| rs583129101 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152809308 | TAGTCAGGGTTTCTA[C/T]TCCTGCACAAACATC | 17970 |
| rs583259192 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152826929 | GATGGCATCAGATTT[C/T]GTTACGGATGGTTGT | 17970 |
| rs583328286 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152827980 | GGACAGCCAGGGCTA[C/T]ACAGAGAAACCCTGT | 17970 |
| rs583376504 | snp | A/C/T | | | upstream-variant-2KB | Ncf2 | GRCm38.p3 | 1:152799451 | CTGATTCTCCCCCCC[A/C/T]CCCCCCAAGACAGGG | 17970 |
| rs583398182 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815775 | CCAGGCAAATGATTC[A/G]TGCAATGGACATCGG | 17970 |
| rs583406655 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152802477 | TTGGTTTTGGTTTTT[C/T]GAGACAGGGTTTCTC | 17970 |
| rs583510008 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812650 | AAGGAAGAAAGGAAG[A/G]AAGAAAGAAAGGAAG | 17970 |
| rs583514147 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152833949 | CCCCATGAAGTCGGG[A/C]GCTGGGGATGCAGCA | 17970 |
| rs583616366 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152832807 | ATCCAGTGTCCCTCA[C/T]AGTTTTTTTTCTTAC | 17970 |
| rs583622430 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152802777 | GTCACTATTTTATGG[C/T]TCTACAAGATCATTA | 17970 |
| rs583674945 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152811854 | CACACACACACACAT[A/G]TACACACAGATATAT | 17970 |
| rs583902785 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152801477 | GGGGTAGGCTGGGAG[A/G]ATGGATAACAGTAAA | 17970 |
| rs583959725 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152819275 | CATCTTTCCTTCCTT[C/T]CTTTCTTTCTTTCTT | 17970 |
| rs583975403 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152809234 | TCGATCTCACAGCTC[C/T]GCGGGAGCTTCACCT | 17970 |
| rs584217455 | snp | A/C/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152828035 | AAAAAAAAAAAAAAA[A/C/G]AAAAGAAAAGAAAAG | 17970 |
| rs584485878 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152809501 | CTTGCTCAGCCTGCT[C/T]TCTTATAGAACCAAG | 17970 |
| rs584499036 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152801462 | CCGGTGGGGTGGGGT[A/G]GGGTAGGCTGGGAGG | 17970 |
| rs584505206 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152831436 | GGTTTTCAGCATGGT[C/T]GAAAAGATGGCAAAG | 17970 |
| rs584579353 | snp | C/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152803532 | GAACCAATTAGAACA[C/G]TTGCCAGGATGTGGA | 17970 |
| rs584580400 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152818778 | GCCAGGCAAGGTGGT[A/G]CGCGCCTTTAATCTC | 17970 |
| rs584707095 | snp | C/T | | | upstream-variant-2KB | Ncf2 | GRCm38.p3 | 1:152798510 | CCAGTATTTAAAACG[C/T]TTGCTTTAAATTTGA | 17970 |
| rs584795090 | snp | A/C | | | upstream-variant-2KB | Ncf2 | GRCm38.p3 | 1:152798209 | ACCTTATCTCGAAAA[A/C]CAAAAAAAAAAAAAA | 17970 |
| rs584799447 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152813058 | TGAACTCAGGACCTT[C/T]AGAAGAGCAGTCAGT | 17970 |
| rs584944780 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152829650 | GTGACTAGACTGTAG[C/T]TGTCTTCAGACACAC | 17970 |
| rs585205352 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152809535 | ACCAGCCCAGAGATG[A/G]CACCACCCACAAGGG | 17970 |
| rs585229189 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152822572 | CTGTATTGTTTTTTT[G/T]TTTTTTTTTTGCGGG | 17970 |
| rs585339134 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152819175 | TGTGACCCTTTAATC[A/G]CCTGGTGACCTTTGT | 17970 |
| rs585387295 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152831703 | AGGTTGGTGGCCCCG[A/G]GGAAGGAGCTCTCTC | 17970 |
| rs585414973 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152818944 | AAAAACAAAACAAAA[A/C]AAAAAAACAAAAAAA | 17970 |
| rs585487641 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152826299 | CTCCTGTATAAGAGA[C/T]TCCTTTGGGAACACA | 17970 |
| rs585587893 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152804791 | CAACCCTACATCCCC[A/G]ACTTGGATTGGGGAC | 17970 |
| rs585709793 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152802465 | TTGTTTTGTTTTTTG[G/T]TTTTGGTTTTTCGAG | 17970 |
| rs585825541 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152806922 | AGAGGCTATGCAATA[A/G]CACCTTCCTCCTCCT | 17970 |
| rs585921756 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152824633 | CGGGAGAGGGCCAGC[A/G]GGAGATGCCCTTGGC | 17970 |
| rs585951661 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152815138 | TGTCAACCCAAAAAA[A/G]GGAGCAGGGTATGTG | 17970 |
| rs586034757 | snp | C/T | | | upstream-variant-2KB | Ncf2 | GRCm38.p3 | 1:152799449 | TTCTGATTCTCCCCC[C/T]CACCCCCCAAGACAG | 17970 |
| rs586160024 | snp | C/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152802478 | TGGTTTTGGTTTTTC[C/G]AGACAGGGTTTCTCT | 17970 |
| rs586271329 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152817271 | CCCGGCATGGCATGC[G/T]TGAGGCCCAGGATCT | 17970 |
| rs586310122 | snp | C/T | | | upstream-variant-2KB | Ncf2 | GRCm38.p3 | 1:152799446 | AAATTCTGATTCTCC[C/T]CCCCACCCCCCAAGA | 17970 |
| rs586374680 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152808698 | GGATAGGGCATTTCA[G/T]CATCTTTTTTTGTTT | 17970 |
| rs586412551 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812014 | CAAGTGTGGTGAGGC[G/T]GGGGTGCGGGAAGCA | 17970 |
| rs586512441 | snp | A/G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152802282 | GAGAGAGAGGGAGAG[A/G/T]GAGAGAGAGAGAGAG | 17970 |
| rs586543160 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152818888 | GGCTACACAGAGAAA[C/T]CCTGTCTCGAAAAAA | 17970 |
| rs586626756 | snp | A/G | | | upstream-variant-2KB | Ncf2 | GRCm38.p3 | 1:152799659 | GGCTGGGAGTGTTTC[A/G]GTCCAAATGTGGGCC | 17970 |
| rs586655073 | snp | A/G | | | utr-variant-5-prime | Ncf2 | GRCm38.p3 | 1:152800185 | GAGGTCCCTGACTCT[A/G]GCTGTGCTCTCTCTC | 17970 |
| rs586661357 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152827999 | GAGAAACCCTGTCTC[A/G]AAAAACAAAAAAAAA | 17970 |
| rs586677430 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812658 | AAGGAAGAAAGAAAG[A/G]AAGGAAGGAAGGAAG | 17970 |
| rs586720856 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152809237 | ATCTCACAGCTCCGC[A/G]GGAGCTTCACCTGCT | 17970 |
| rs586828120 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152820296 | GCACCAGCACCAGCT[A/G]TTACCTCCATGGAAA | 17970 |
| rs587050992 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152812607 | AGGAAGGAAGAAAGA[A/G]AGAAAGAAAGAAAGG | 17970 |
| rs587131032 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152827871 | ATCCTTCTAGCCAGG[C/T]GTGGTGGTGCACGCC | 17970 |
| rs587138324 | snp | A/G | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152800669 | GATGTTTCTGTCGGA[A/G]TGTTTTACCACAGCA | 17970 |
| rs587158994 | snp | A/C | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152809370 | TTTATTCGGCTTACA[A/C]TTCCATCCTGCTGTT | 17970 |
| rs587216529 | snp | A/G | | | utr-variant-3-prime | Ncf2 | GRCm38.p3 | 1:152836444 | CCAACAGTTCAGTGG[A/G]AAAATAATTAATAAA | 17970 |
| rs587350689 | snp | G/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152833245 | GATCCACCCTGGATG[G/T]TAAAGGGTAGGGAGA | 17970 |
| rs587498008 | snp | C/T | | | intron-variant | Ncf2 | GRCm38.p3 | 1:152819311 | CTTTCTTTCTTTCTT[C/T]CTTTCTTTCTTTTGT | 17970 |