SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3674858 | snp | C/G | 0.495868 | 0.0452663 | intron-variant | Nod2 | GRCm38.p3 | 8:88654038 | TGGACAGAAAAGTAT[C/G]GCTGTGTATGTCTGA | 257632 |
rs3674878 | snp | C/G | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88654048 | AGTATGGCTGTGTAT[C/G]TCTGAAACTTATATT | 257632 |
rs3700029 | snp | A/G | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88658528 | acctatctgtccatc[A/G]tccatccatctgccc | 257632 |
rs3700594 | snp | C/T | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88658623 | TACTGCCTCTGTCAT[C/T]GGGACTAAATCAGTG | 257632 |
rs3700655 | snp | A/G | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88658662 | AGAAAACTTTGTTGT[A/G]ATGTTCATACCTCAG | 257632 |
rs3701099 | snp | A/G | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88658682 | TCATACCTCAGCTGG[A/G]GATAGATCATAGCAG | 257632 |
rs3701243 | snp | C/G | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88658751 | TGGAAGATTAATAAA[C/G]GAGTGGATCTGTCTG | 257632 |
rs3701800 | snp | A/G | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88658812 | TTCACCTTCCTGAAA[A/G]GTTGTTAGAGTATTC | 257632 |
rs4136007 | snp | C/T | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88658554 | tgcccatccatccat[C/T]catccatccatccat | 257632 |
rs6155594 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Nod2 | Mm_Celera | 8:88653488 | CCGTGGCAGCCCAGA[A/G]CTTGGCCTCAGTTGC | 257632 |
rs13479904 | snp | A/G | 0.393491 | 0.20472 | missense | Nod2 | GRCm38.p3 | 8:88663745 | AGGACCATGGTGTTG[A/G]CTCAGTCTCGCTTCC | 257632 |
rs32536897 | snp | A/C | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88661294 | ATATAACTGGGAAGA[A/C]ACCTAATATAGACTT | 257632 |
rs32572980 | snp | A/T | 0.5 | 0 | intron-variant | Nod2 | Mm_Celera | 8:88678995 | TTTTTTTTTTTTTTT[A/T]ACTGAAGGTTGGACT | 257632 |
rs32574918 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Nod2 | GRCm38.p3 | 8:88674287 | GAGCTCTTGCTAACA[C/G]CCGCAGGGGCAGGCT | 257632 |
rs32577206 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Nod2 | GRCm38.p3 | 8:88647985 | CACCCACGGTTGATA[C/T]CCTGCAGGGGAAATG | 257632 |
rs32581751 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88655629 | GGGACTGAGGTAGCA[A/G]TGTGAGCTCTGACTT | 257632 |
rs32583224 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Nod2 | Mm_Celera | 8:88673758 | GATTGGGTGGCTTTA[C/T]GTAATCTATTTGACA | 257632 |
rs32584185 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Nod2 | GRCm38.p3 | 8:88679320 | TTCCTCTAAACCTTT[A/C]ACTGTTTTCAGGGGA | 257632 |
rs32595398 | snp | G/T | 0.432133 | 0.171253 | intron-variant | Nod2 | GRCm38.p3 | 8:88675069 | AGTTCATTGAACTTT[G/T]TGTATGCACTCCATT | 257632 |
rs32600928 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Nod2 | GRCm38.p3 | 8:88680056 | CTGGTCTGGTTTCAG[A/C]ACCTTCTTTGTAGTT | 257632 |
rs32602113 | snp | C/G | 0.401235 | 0.199068 | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88647220 | ACTGCAGGCAGGCCT[C/G]TTCCCGGATACCTGT | 257632 |
rs32608202 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Nod2 | GRCm38.p3 | 8:88675362 | CTTCATTTGCTTGTC[C/T]GTCACTCGCCCTTCA | 257632 |
rs32613962 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88673408 | CTTTTATGGTTTTTC[C/G]AGACAGAGTTTCTCT | 257632 |
rs32619247 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Nod2 | GRCm38.p3 | 8:88648102 | GCTCCCAGTTTCTTG[A/G]CCACTTAATGCCAGT | 257632 |
rs32621110 | snp | A/G | 0.5 | 0 | missense | Nod2 | GRCm38.p3 | 8:88663830 | ACATCTTGGAGCTGC[A/G]GACTGAAGTGGGCAC | 257632 |
rs32630558 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Nod2 | Mm_Celera | 8:88679702 | TATGGTGTGTGACAC[A/C]ACTTCTCCTGGTGAG | 257632 |
rs32631169 | snp | G/T | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88660402 | TGTCAGCACTTAGAA[G/T]GGTTGGGATTTAAGA | 257632 |
rs32636356 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88661049 | CAGTGAGAGAGGCTC[C/G]GGTGACACGGCTAAA | 257632 |
rs32639911 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88674521 | ACATGATAGAAACAG[A/G]GGGGATTAAGAAGGA | 257632 |
rs32653748 | snp | A/G | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88669138 | GGTGAAATTAATGAT[A/G]CTACTGTTGGGGGGG | 257632 |
rs32656069 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88661583 | CCAATTAAGCAGGTG[A/G]ACATGGTTGTACACA | 257632 |
rs32657909 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nod2 | Mm_Celera | 8:88666811 | ACAGACACCTTTGTG[A/C]AACTGTGTGTTGACT | 257632 |
rs32664746 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Nod2 | GRCm38.p3 | 8:88656475 | AGAAGGCTAAGCAGG[C/T]GTATAGAAAATGTAA | 257632 |
rs32674247 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Nod2 | GRCm38.p3 | 8:88679426 | CCTGGGATTCTTCCC[A/G]TAGACACTCCTAATT | 257632 |
rs32682906 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Nod2 | GRCm38.p3 | 8:88671086 | GTGGTACCCAGGTGC[C/T]GGAATGTTCCCCAGA | 257632 |
rs32690189 | snp | A/T | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88653650 | GCTCTTCCCCAGCCA[A/T]AACCTCTACCCTTCA | 257632 |
rs32694333 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88682177 | AACCTGGCAGTTGCA[A/T]CCCTTTTGGGGGTTC | 257632 |
rs32698083 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nod2 | Mm_Celera | 8:88667266 | TTTGGCTAGGAAAAT[G/T]AATGAACATGATCTG | 257632 |
rs32698902 | snp | A/G | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88661228 | TACTTGGGAGAAGAA[A/G]CCACCAGTTGCAGAA | 257632 |
rs32724915 | snp | C/T | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88686577 | ACTTTCCTTGCAAGC[C/T]TTCACTCACACCTCC | 257632 |
rs32745202 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88652715 | TCATGGCAACTGCAG[C/T]TAGCTTTTGATATCC | 257632 |
rs32753404 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88674856 | CGGAGTGGCGCTATG[A/G]AAGCACATGAACACG | 257632 |
rs32759574 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88666147 | CCACAACCATGCTGG[A/G]CTCAGCAGGGCTCTT | 257632 |
rs32773589 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88668957 | TGAAAACCACTTCCC[C/T]GAGAGCCCTAGAAAA | 257632 |
rs32791473 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88682247 | AGCACAGATGTTTAC[A/G]TTAAGACTTATAACA | 257632 |
rs32799724 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88682020 | CTCGACACATATCCA[A/C]TCCAAGAGTGGAGCT | 257632 |
rs32800817 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Nod2 | Mm_Celera | 8:88679082 | TTATCCAATTAAATC[A/G]TCAAATCAGAGGCCA | 257632 |
rs32807483 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88660951 | GGATCTCTCAATCCA[C/T]GAAACGTAGTTTCTC | 257632 |
rs32810926 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Nod2 | GRCm38.p3 | 8:88674386 | GAGAGTGCTATGCAG[A/G]CCCAGTGCAGATGTC | 257632 |
rs32848034 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Nod2 | GRCm38.p3 | 8:88652655 | CTGTAGCAAGAGTAC[A/G]GGAGCCCAGGGACTC | 257632 |
rs32848035 | snp | A/G | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88682603 | TGTGTTCAGACATTG[A/G]TTGGAAAAATATTGG | 257632 |
rs32854334 | snp | C/T | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88648010 | GAAATGCCCCCTCCC[C/T]CATCTCTGCCCTCCT | 257632 |
rs32855240 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Nod2 | GRCm38.p3 | 8:88679268 | GCTGCTTGCCAACCG[C/T]CTTGACTCTTGTATG | 257632 |
rs32858426 | snp | C/T | 0.5 | 0 | synonymous-codon | Nod2 | GRCm38.p3 | 8:88664365 | CCTCAGGAAGTTCGT[C/T]CGTACAGAGTGCCAA | 257632 |
rs32861288 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Nod2 | GRCm38.p3 | 8:88674851 | TGGGGCGGAGTGGCG[C/T]TATGGAAGCACATGA | 257632 |
rs32868886 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nod2 | Mm_Celera | 8:88666911 | TAGCTCTGTTGCACA[C/T]AATAACTGTATAATA | 257632 |
rs32903994 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nod2 | Mm_Celera | 8:88653337 | GTCTCAGAGGGTAAG[C/G]TGTGGCCTGTGTCAG | 257632 |
rs32914338 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88661062 | TCCGGTGACACGGCT[A/G]AAATGTACCAGGCAG | 257632 |
rs32923110 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88661082 | GTACCAGGCAGCCTG[C/G]CATACACTCTATGGA | 257632 |
rs32926486 | snp | A/G | 0.375 | 0.216506 | synonymous-codon | Nod2 | Mm_Celera | 8:88663780 | TACTTACGATGGGTC[A/G]GAGAATCTTTGCCTG | 257632 |
rs32929914 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Nod2 | GRCm38.p3 | 8:88673328 | AGAAACAAGGCCTTA[C/T]TGCCATGGAGCTCTC | 257632 |
rs32933916 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nod2 | GRCm38.p3 | 8:88673846 | ACAATGCCTTATCTA[C/T]AGAGCAGTGTTCCCA | 257632 |
rs32934188 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88666874 | TAACATAATATGGTG[A/T]GTTGTATATGCAGTT | 257632 |
rs33005423 | snp | A/G | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88674041 | AATACCATGGTGGCA[A/G]GAGGTTGTGGGAGAG | 257632 |
rs33025491 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Nod2 | GRCm38.p3 | 8:88652303 | TACAGAGGCAGGGCT[A/G]CGGGGATAACCAAAG | 257632 |
rs33029774 | snp | A/C | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88652250 | TTGGCATCTTTACAG[A/C]AATCCCCAGATCTAT | 257632 |
rs33110890 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88673387 | GGACATTTATGTACC[A/G]CCTAGCTTTTATGGT | 257632 |
rs33112860 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nod2 | Mm_Celera | 8:88674373 | TTTCAGAGTGCGTGA[A/G]AGTGCTATGCAGACC | 257632 |
rs33148979 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nod2 | Mm_Celera | 8:88675150 | AACTTGAGGGTTTGG[C/G]GGTGAATTTGGAGGT | 257632 |
rs33149135 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88655585 | TGATGCCAGCTGTCC[C/G]TGTGACTCATGCAGA | 257632 |
rs33152263 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Nod2 | GRCm38.p3 | 8:88674992 | TAAAGTGGCTCAGGT[A/G]AGTTGCAAGATGTGT | 257632 |
rs33173211 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Nod2 | GRCm38.p3 | 8:88680202 | TTGTTTACCTTCTTG[C/T]TTAAGGAGTCTCCCT | 257632 |
rs33177612 | snp | C/T | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88679424 | ATCCTGGGATTCTTC[C/T]CGTAGACACTCCTAA | 257632 |
rs33204454 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Nod2 | GRCm38.p3 | 8:88652609 | GGAGGGAACTGACCC[A/G]CAGAAGCTGGCTTCT | 257632 |
rs33208275 | snp | C/T | 0.5 | 0 | synonymous-codon | Nod2 | GRCm38.p3 | 8:88664368 | CAGGAAGTTCGTCCG[C/T]ACAGAGTGCCAACTG | 257632 |
rs33209427 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88673415 | GGTTTTTCGAGACAG[A/G]GTTTCTCTGTGTAGT | 257632 |
rs33210632 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Nod2 | GRCm38.p3 | 8:88680051 | GGCAACTGGTCTGGT[C/T]TCAGAACCTTCTTTG | 257632 |
rs33218695 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88682668 | TACCACAATTCTTAG[A/G]TCAGGTGGCTAGGAC | 257632 |
rs33219591 | snp | C/G | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88680609 | TAGGAACTAGGAGGG[C/G]TTTAGGTAGCTCCAC | 257632 |
rs33236045 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Nod2 | GRCm38.p3 | 8:88673951 | ATAAGCAGCTTTAGG[A/G]AAGATATGTTTATTT | 257632 |
rs33296163 | snp | A/G | 0.5 | 0 | downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88688728 | CTCCTGGTGGCTGTC[A/G]AAGTGAGTAGATGTC | 257632 |
rs33306176 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nod2 | Mm_Celera | 8:88666941 | AGAAATATGAATAGC[A/T]CCATCAGGGTCTTGA | 257632 |
rs33307887 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nod2 | GRCm38.p3 | 8:88667062 | GGGAAAAGCCTGAAG[C/T]GAGAGAGGATTTGCT | 257632 |
rs33318219 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Nod2 | Mm_Celera | 8:88679719 | CTTCTCCTGGTGAGA[C/T]GTAATGTACAAGTCT | 257632 |
rs33321591 | snp | A/G | 0.5 | 0 | synonymous-codon | Nod2 | GRCm38.p3 | 8:88660616 | GCACGTCAGGGAACT[A/G]CCAGCTCCACTGCCT | 257632 |
rs33338846 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88674309 | GGGCAGGCTGTATTT[C/T]TTAAGTATTTCTTGG | 257632 |
rs33344760 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nod2 | GRCm38.p3 | 8:88667524 | ATGCGCCACCACGCC[C/T]GGCAGGGCCACTCCT | 257632 |
rs33403077 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88681920 | CAGAAAGGGCTGGCG[A/C]CTGTGGAAGGTGGAT | 257632 |
rs33425875 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nod2 | GRCm38.p3 | 8:88655656 | ACTTGCTTGCTTCTG[C/T]CATAGAACCACTAAG | 257632 |
rs33427249 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Nod2 | GRCm38.p3 | 8:88681995 | AGCCTTCGGGAGTTG[A/G]CAGAACAAGCTCGAC | 257632 |
rs33437194 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nod2 | GRCm38.p3 | 8:88660807 | AAAAGATGAGGGCAT[A/G]GCGGCTCTCCCCCTT | 257632 |
rs33450100 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Nod2 | Mm_Celera | 8:88668992 | TCGGGGAGGCTGCAC[C/T]GTGCTGTGCTTAAGC | 257632 |
rs33471863 | snp | A/G | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88669133 | CTTGGGGTGAAATTA[A/G]TGATACTACTGTTGG | 257632 |
rs33480353 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88655209 | TTGACCTTTTAATTT[C/T]TTTATAGAGGTGGCT | 257632 |
rs33494486 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Nod2 | GRCm38.p3 | 8:88682597 | TATGTGTGTGTTCAG[A/C]CATTGATTGGAAAAA | 257632 |
rs33498355 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nod2 | Mm_Celera | 8:88661770 | CCAAATTTCATTTTG[C/T]CTACTTATTTTTTTT | 257632 |
rs33500855 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Nod2 | GRCm38.p3 | 8:88679174 | TCTCTGATTTACACA[A/G]CCAAGCTCCTGATTG | 257632 |
rs33503962 | snp | C/G | 0.396694 | 0.202437 | intron-variant | Nod2 | GRCm38.p3 | 8:88673392 | TTTATGTACCACCTA[C/G]CTTTTATGGTTTTTC | 257632 |
rs33573501 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Nod2 | Mm_Celera | 8:88669007 | TGTGCTGTGCTTAAG[C/G]GCAGGTTGGCAGCCC | 257632 |
rs33576011 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Nod2 | GRCm38.p3 | 8:88675381 | ACTCGCCCTTCATAG[G/T]TCAGTTGACCAGTCT | 257632 |
rs33580812 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88661092 | GCCTGGCATACACTC[C/T]ATGGAAATTTTCTGC | 257632 |
rs33596403 | snp | A/G | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88661302 | GGGAAGAAACCTAAT[A/G]TAGACTTCTGGTCCA | 257632 |
rs33607338 | snp | G/T | 0.375 | 0.216506 | downstream-variant-500B | Nod2 | Mm_Celera | 8:88688823 | CAGACACAAGACTTA[G/T]TCTTGCTATGCCCAT | 257632 |
rs33611291 | snp | A/G | 0.5 | 0 | intron-variant | Nod2 | Mm_Celera | 8:88660194 | GGTTGTATTGTTGGT[A/G]GTTTTTACTTTATCC | 257632 |
rs45639741 | snp | G/T | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650940 | GAGACCTTCTCTCCT[G/T]CGCTGCCAGATACTC | 257632 |
rs45695672 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Nod2 | GRCm38.p3 | 8:88668596 | AGAAGGGGTCAGCTT[C/T]TCTCCCACAGTATGA | 257632 |
rs45781190 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88678125 | ACATAGCTATTTAGC[C/T]TGTCTTACAAGGATC | 257632 |
rs45786439 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88678465 | TCAATCAGGTCCTTG[A/C]TGCATCAACCTTCTC | 257632 |
rs45792107 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Nod2 | Mm_Celera | 8:88670693 | ACTCACGGATGCGTG[C/T]GCCTGCTCCATGGCC | 257632 |
rs45798350 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662957 | TTCATTACAACAATG[A/G]ATGGGAGGCAGAGAG | 257632 |
rs45820839 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662630 | CAAGAAGGAAGTATC[A/G]GAAGGTTTTGACGAG | 257632 |
rs45825508 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662889 | ACAATGTGGCCAGGA[A/G]GGTTGGTGGCTGGTG | 257632 |
rs45883803 | snp | G/T | 0.444444 | 0.157135 | synonymous-codon | Nod2 | GRCm38.p3 | 8:88665229 | CATCCCGCCTGCCGT[G/T]CCCGGTGAGACCAAG | 257632 |
rs45902770 | snp | C/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88672066 | ACAGGTCTTGGGTTA[C/G]CTTCTTGGTACCACA | 257632 |
rs45917843 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Nod2 | GRCm38.p3 | 8:88659111 | GAGTGTTTACCATTG[G/T]ACTCAGGCCATGGCT | 257632 |
rs45929016 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88685080 | GGTTTAGTTGCCGGG[C/T]ATGGTGGAGCACGCC | 257632 |
rs45944626 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88657968 | AGGCAGGGACAGTGA[A/G]TGGCTGGGTCATGCT | 257632 |
rs45974196 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nod2 | Mm_Celera | 8:88672199 | GAAAGCTTGCCTTGT[G/T]GGTGACAGCTCTGAA | 257632 |
rs45976970 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88656896 | GAAATTTCACTGATG[A/G]GTCTACTGATGATTT | 257632 |
rs45978800 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661048 | GCAGTGAGAGAGGCT[C/T]CGGTGACACGGCTAA | 257632 |
rs45984388 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88657149 | AGTACTGAGATTACA[A/G]GCATAATCCACCACA | 257632 |
rs45990546 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nod2 | Mm_Celera | 8:88654359 | TTCACAGAACACGCA[C/T]AGTCTTCTCATTCCT | 257632 |
rs46019695 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Nod2 | Mm_Celera | 8:88675633 | GGCTTTGAGTCGTGC[A/G]CCTGCAGACCCTGGT | 257632 |
rs46037902 | snp | C/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88659427 | TATGTTGACCGTGTG[C/G]TGAAATGGCAGGATT | 257632 |
rs46060809 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Nod2 | Mm_Celera | 8:88651970 | GTTACAAACTGGCCT[A/C]TTTCTCTGCCGCGTA | 257632 |
rs46087709 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88655495 | CTTTGTGTCATAAGA[C/T]ATGAGAGCTTTGTAT | 257632 |
rs46099036 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88649276 | AGAGCAGCTGGGAAG[C/T]AGGGAAGAATATCAG | 257632 |
rs46105686 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nod2 | GRCm38.p3 | 8:88678462 | CCATCAATCAGGTCC[C/T]TGCTGCATCAACCTT | 257632 |
rs46107257 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88678161 | CTGCTTAAAGCCCTC[A/G]TGAGCCTTTTTGTCC | 257632 |
rs46112995 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88681052 | TACCAGGGCCTCGCC[C/T]GTCTCCATCTCTTCC | 257632 |
rs46133603 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Nod2 | GRCm38.p3 | 8:88657573 | GTAAGCCTTGGTTAT[C/G]TGTCTTATTATTAAA | 257632 |
rs46169263 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88655449 | AGGAACTGGATCTCT[C/G]TCTGTTTCTTTCCAA | 257632 |
rs46185906 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Nod2 | GRCm38.p3 | 8:88675751 | CAAACTCTGGAATCA[A/C]ACAGGCAGATTAAAG | 257632 |
rs46214279 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nod2 | GRCm38.p3 | 8:88677940 | AACTGTTAGAGATTT[C/T]ACCTCTTGCAGTTGC | 257632 |
rs46238403 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662699 | GTTAGCCTTTCAGTC[C/T]GACTAATCCATTTAG | 257632 |
rs46247349 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88668380 | AGAGAAAGCTGAATG[C/T]GGCGCTTAAAGCCCT | 257632 |
rs46260981 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88670245 | TCACCAGCTCCCCTG[A/G]CCAGGGATTTTGGAT | 257632 |
rs46270618 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662491 | GATGTCCTGTGACGT[C/T]CTGCCAGCCTGAGCC | 257632 |
rs46273238 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88674177 | CATACTCCTATTTCA[C/T]CGCCTGCCACTAATG | 257632 |
rs46298970 | snp | G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88657216 | CCTGAATTCTTGAGG[G/T]TTCCATCTATGCTTT | 257632 |
rs46354676 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88657643 | CTGTCTACAGTGACT[A/T]TCACCGTAGATGGTT | 257632 |
rs46365999 | snp | C/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650040 | TCTTCTTTTCCAGCT[C/G]TTTGGGATGAGATAG | 257632 |
rs46376016 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88679626 | ACCTAGAGCTAGGAC[A/C]TTGCATTTGCTCCTC | 257632 |
rs46409399 | snp | A/C | | | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88645626 | ATGGTGAAAAGAGAA[A/C]TGAGTCCTCCAAGTT | 257632 |
rs46431499 | snp | A/G | | | synonymous-codon | Nod2 | GRCm38.p3 | 8:88665148 | GGTCTCCGAGAGGGT[A/G]CTGCTCCAGCGTCAG | 257632 |
rs46447251 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nod2 | Mm_Celera | 8:88669747 | TGGGCTGGTAACCAC[C/T]TATGCAAGGATTACT | 257632 |
rs46450454 | snp | A/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88649981 | CTGGGACTAACTAAT[A/G]AAGAACTTCTTCAGC | 257632 |
rs46476621 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nod2 | Mm_Celera | 8:88678474 | TCCTTGCTGCATCAA[C/T]CTTCTCTTTAATTTC | 257632 |
rs46483315 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88672002 | TTTGGTGCCACTCTG[C/T]AAGAATTCATGAGGC | 257632 |
rs46518032 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88665535 | GTGACAAGGTCTTGC[C/T]GATTGGGCCTGTGGC | 257632 |
rs46518263 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nod2 | Mm_Celera | 8:88673204 | AGATGTTTTGACCCA[C/T]TGCTCTGGCAAGTTA | 257632 |
rs46520281 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88671762 | AACGCACGCAACGAG[C/T]TGGTACAGTACAGTG | 257632 |
rs46526992 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88672067 | CAGGTCTTGGGTTAG[C/T]TTCTTGGTACCACAT | 257632 |
rs46537276 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88678766 | TTTCTGCCTCCACAG[A/C]AGACTGATGGATCCT | 257632 |
rs46552613 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nod2 | Mm_Celera | 8:88669968 | GCAGTGCTCGTTAAC[A/T]TAGGCCTGTTTCCAA | 257632 |
rs46579993 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nod2 | Mm_Celera | 8:88672065 | CACAGGTCTTGGGTT[A/T]GCTTCTTGGTACCAC | 257632 |
rs46599733 | snp | A/G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88684262 | GAAGCCTGGCAATGA[A/G/T]CTGTGGCTCCTCAGC | 257632 |
rs46607366 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650941 | AGACCTTCTCTCCTT[A/C]GCTGCCAGATACTCA | 257632 |
rs46632764 | snp | A/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685088 | TGCCGGGTATGGTGG[A/C]GCACGCCTTTAATCC | 257632 |
rs46633300 | snp | C/T | 0.473373 | 0.11227 | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650973 | GTAGCTTCGCTGCCT[C/T]GGCTTTTCCCTGTCT | 257632 |
rs46635585 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88648448 | GCTGGGACAGGGCTT[A/G]GGGGCTACAGTTTTG | 257632 |
rs46647920 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662472 | GAAGGTGTTGACATC[C/T]TATGATGTCCTGTGA | 257632 |
rs46657266 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Nod2 | GRCm38.p3 | 8:88678636 | TCAGACGCTGATAAC[A/C]AATTGTCCTTACGGC | 257632 |
rs46686292 | snp | A/G/T | 0.132653 | 0.220748 | intron-variant | Nod2 | GRCm38.p3 | 8:88652027 | GGTCCCTTCCTCACC[A/G/T]AGTCCCCAGCACTCG | 257632 |
rs46691768 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88681207 | AGCACCTCCCTTTCC[A/G]AAGCGTTCCTGGAAG | 257632 |
rs46700321 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88646732 | TCCTCATATCTACAA[C/T]ACAAATCTTCGGAAC | 257632 |
rs46714434 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Nod2 | GRCm38.p3 | 8:88657520 | TTCTCTATTAATTTG[A/T]CTCTGATCTCCCATT | 257632 |
rs46717106 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88674634 | AGATGATAGCTACCA[A/G]GAAGCAAATCTTGAC | 257632 |
rs46734485 | snp | G/T | 0.495868 | 0.0452663 | intron-variant | Nod2 | GRCm38.p3 | 8:88676399 | CCAGATAGGAGCCCA[G/T]GATGGATGCCACTGA | 257632 |
rs46742708 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685749 | CAGACTGGCTTCAAA[C/T]TCACTGTGTAGCCAA | 257632 |
rs46754075 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Nod2 | Mm_Celera | 8:88676484 | GAGGGCTTACTTACA[A/G]GAACAGAAATGACTC | 257632 |
rs46844556 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nod2 | GRCm38.p3 | 8:88670769 | TGGACTTCCCTTCTT[C/T]TCTGAATCCGACATT | 257632 |
rs46925012 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88647160 | GTTCCCAGGACTCTG[A/G]TTCCCTTGTGATTGA | 257632 |
rs46946811 | snp | A/G | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650387 | AGCCAGTGTAGATGT[A/G]CCAGTTTTTGTGCCA | 257632 |
rs46989866 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685156 | TCAAGGTCTTCAAAG[C/T]GAGTTCCAGGACAGC | 257632 |
rs47044770 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88669067 | CAGCAAAGTCACCCC[A/C]TTTTGTTTGTGTCTC | 257632 |
rs47053829 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88663581 | GGCAGGACAGATGCC[C/T]ACTAGGACAGATGCC | 257632 |
rs47074997 | snp | C/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88649867 | TAAGAGTGACTCCAA[C/T]GTGGCACTAGCCTGG | 257632 |
rs47094628 | snp | A/G/T | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650677 | GGCAAGAGTGCTAAC[A/G/T]TCACCTCTGTGCTTT | 257632 |
rs47101855 | snp | C/T | | | synonymous-codon | Nod2 | GRCm38.p3 | 8:88665466 | CTCTGTGGGAGATGT[C/T]GGAGTGGAACAGCTG | 257632 |
rs47130395 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650871 | TCCTCCTGGGCTGAG[C/T]ACAGGGTACAGGTGA | 257632 |
rs47136293 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88669536 | ACCTGCTGCCAATGC[C/T]TCCCTGCTAGTGTAG | 257632 |
rs47156375 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nod2 | Mm_Celera | 8:88673588 | GTCTGGGTCAGGGAT[A/G]GCACCAGGAACTGAA | 257632 |
rs47159462 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nod2 | Mm_Celera | 8:88655857 | CTGGTGCTTTTCTTT[A/G]TGGTTTCTATGCCTT | 257632 |
rs47169787 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Nod2 | Mm_Celera | 8:88669493 | GTCTTTGTGCTTACC[G/T]TTGGAGATGTAAGCT | 257632 |
rs47190661 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Nod2 | GRCm38.p3 | 8:88676551 | GTGGCAGCTCATCTG[C/T]GCACACTGCACAGCC | 257632 |
rs47202982 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88649283 | CTGGGAAGCAGGGAA[A/G]AATATCAGTGAAACC | 257632 |
rs47229205 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88672033 | TACTGGGGTGGTCTC[A/G]AAGCTAACTTGCCCA | 257632 |
rs47239952 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nod2 | Mm_Celera | 8:88676883 | TACCTTCTTTTTGTC[A/C]CTCTTTGAGCCTTGG | 257632 |
rs47248380 | snp | A/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662511 | CAGCCTGAGCCTCTG[A/C]CCAGCACTTCCCCAT | 257632 |
rs47255608 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Nod2 | Mm_Celera | 8:88658009 | GAAGACATACTTGAT[A/G]CTGCCATGCCAGAGC | 257632 |
rs47267373 | snp | C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650878 | GGGCTGAGTACAGGG[C/T]ACAGGTGACATGCTT | 257632 |
rs47269743 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nod2 | GRCm38.p3 | 8:88683340 | AGCATACCATGCATG[C/T]GTGAAGCAGCAAGTG | 257632 |
rs47290241 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88677097 | CTATGATGACCTCCT[C/G]GACCATCCTGACGTA | 257632 |
rs47324982 | snp | A/G | | | synonymous-codon | Nod2 | GRCm38.p3 | 8:88665067 | GCCACACAACCTGCA[A/G]ATCACAGCAGCCTTC | 257632 |
rs47342648 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nod2 | Mm_Celera | 8:88652654 | ACTGTAGCAAGAGTA[C/T]GGGAGCCCAGGGACT | 257632 |
rs47350757 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88671906 | AAAATGCCCACGGGT[A/G]GTGGGAGAATGAGGA | 257632 |
rs47363666 | snp | C/T | | | utr-variant-3-prime | Nod2 | GRCm38.p3 | 8:88687700 | GAATGGCCAGGATTC[C/T]GAAGGGTTCAGTGGA | 257632 |
rs47365765 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88675616 | AGTCATCAGCCGATT[C/T]TGGCTTTGAGTCGTG | 257632 |
rs47412488 | snp | A/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650082 | TCTTAGAGGCAGAGG[A/G]CTGGCAGAATTGGTC | 257632 |
rs47423345 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Nod2 | Mm_Celera | 8:88675748 | CCACAAACTCTGGAA[G/T]CACACAGGCAGATTA | 257632 |
rs47430096 | snp | G/T | 0.391111 | 0.206368 | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88646863 | TTTTTAGAAGTAACA[G/T]TAAGAATGGGAACTA | 257632 |
rs47498576 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685904 | GCCCTTCTTAGGTGG[A/G]CAGACTCTTAGAGCT | 257632 |
rs47525180 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685422 | GTTTGAAGAAGGCAT[C/T]CAGAGTCAACCTGAT | 257632 |
rs47531579 | snp | A/G | | | synonymous-codon | Nod2 | GRCm38.p3 | 8:88665178 | GGCACGTGCCCGCTC[A/G]TGTCTGGCCCACAGC | 257632 |
rs47538495 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88672667 | GATCTTCTGTGTCTT[C/T]CTGCCAGGGTGGGGA | 257632 |
rs47549639 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Nod2 | GRCm38.p3 | 8:88678027 | AGAACCATTTGTCAG[G/T]CTGTTTTTGCCATTG | 257632 |
rs47572763 | snp | A/G | 0.124444 | 0.216185 | missense | Nod2 | Mm_Celera | 8:88653110 | AAGCTCCTCGAAGCT[A/G]TGCAGGAGGCACAGG | 257632 |
rs47585701 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Nod2 | GRCm38.p3 | 8:88669465 | TTTAGAGTCTTGTCA[C/G]ATGGAGTTCACTGTC | 257632 |
rs47587088 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88681761 | TAGGGTCTGAGATCA[A/G]GCTCTGGCTAGCTCT | 257632 |
rs47613430 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nod2 | Mm_Celera | 8:88670077 | CACAGGCCAGCTCCT[C/G]TCCATCTTAACAGCC | 257632 |
rs47619635 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88676147 | TTTGGGATCACTGAA[C/T]GAGCCACCAAGTGCT | 257632 |
rs47632235 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88654432 | CATTCAAAAGCACAT[A/G]AATAAATCCTCAGTG | 257632 |
rs47674783 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88648366 | TGGGTGATGCACAGG[A/G]ATATGGTGAATACAT | 257632 |
rs47679401 | snp | A/G | | | synonymous-codon | Nod2 | GRCm38.p3 | 8:88665394 | TGCAGAGTGTGCTGC[A/G]CTGGCCTTTGTACTG | 257632 |
rs47705058 | snp | A/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645387 | GTGTGTGTGGGGGGG[A/G]GGCAGCTGGTAGAAA | 257632 |
rs47724652 | snp | C/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645316 | GGCTTTTTTTATTGA[C/T]AGGCAATGCTTTTAC | 257632 |
rs47726661 | snp | A/G | 0.493827 | 0.0552116 | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88645733 | AAACTATTTAAAATC[A/G]AAACTGTTGGGTTTG | 257632 |
rs47744808 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Nod2 | GRCm38.p3 | 8:88657225 | TTGAGGTTTCCATCT[A/C]TGCTTTAACACCTGC | 257632 |
rs47776211 | snp | G/T | | | synonymous-codon | Nod2 | GRCm38.p3 | 8:88665283 | CATTTGGCTCATCCG[G/T]AGCCTGTACGAGATG | 257632 |
rs47806650 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Nod2 | GRCm38.p3 | 8:88678062 | CAGCTATAACCTTTT[A/G]GGCTCTTGGTGATTT | 257632 |
rs47810495 | snp | C/T | 0.165289 | 0.235211 | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646870 | AAGTAACATTAAGAA[C/T]GGGAACTAAACAACG | 257632 |
rs47817074 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658969 | CATGCTCATTAAATG[A/G]GAGGGAGGCCAATGC | 257632 |
rs47846174 | snp | A/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645380 | AAAGCGTGTGTGTGT[A/G]GGGGGGAGGCAGCTG | 257632 |
rs47849356 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nod2 | Mm_Celera | 8:88654682 | AACCAGTGGATGCCT[A/G]TAGATACCCAGAAAG | 257632 |
rs47931469 | snp | A/G | 0.32 | 0.24 | intron-variant | Nod2 | Mm_Celera | 8:88654199 | GGTGAGTGCTTGTTG[A/G]TGAAATAAGTGAGCT | 257632 |
rs47976872 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88649009 | AGGCAGCGTCAAGCA[C/T]GACTCTGAGAGTTCG | 257632 |
rs47990904 | snp | C/G/T | 0.497041 | 0.0383476 | intron-variant | Nod2 | GRCm38.p3 | 8:88670017 | CTAGCTAGCTAGTCT[C/G/T]CAGTCTGCTTTCTAG | 257632 |
rs47996117 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88676866 | CTCTTGTTTTTGACT[C/T]TTACCTTCTTTTTGT | 257632 |
rs48000532 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88678007 | GCCAGCACCCAAACC[C/G]TATGAGAACCATTTG | 257632 |
rs48017015 | snp | A/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88669712 | AAGGTCAGCGCATCC[A/T]GCTGAGGGGGACCAT | 257632 |
rs48021307 | snp | A/G | 0.18 | 0.24 | intron-variant | Nod2 | Mm_Celera | 8:88669531 | TGCTTACCTGCTGCC[A/G]ATGCCTCCCTGCTAG | 257632 |
rs48057574 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Nod2 | GRCm38.p3 | 8:88678595 | CCTCCTCTGTGGTCA[C/T]CCAGTTCCTGATGTT | 257632 |
rs48063609 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88677875 | CCTTGCTCAGGAGAC[A/G]TTCAATCCAGCCCTT | 257632 |
rs48081862 | snp | C/T | 0.32 | 0.24 | missense | Nod2 | Mm_Celera | 8:88653149 | CATACCTTTGAACTG[C/T]ATGGGTCCTGGGACA | 257632 |
rs48094268 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88653534 | CAAGGCCAGTGTGGT[A/G]TGACAGGATGTTTCT | 257632 |
rs48115351 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88685076 | TAGTGGTTTAGTTGC[C/T]GGGTATGGTGGAGCA | 257632 |
rs48123461 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88685089 | GCCGGGTATGGTGGA[A/G]CACGCCTTTAATCCC | 257632 |
rs48204609 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nod2 | GRCm38.p3 | 8:88659380 | AGACATAACAGAAAA[A/G]AGATTAAAAAGCAGC | 257632 |
rs48208465 | snp | C/T | 0.493827 | 0.0552116 | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650880 | GCTGAGTACAGGGTA[C/T]AGGTGACATGCTTGG | 257632 |
rs48224979 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88649931 | AGCCTGGGGAGAGCA[A/G]GTCTGACAAGGGAGG | 257632 |
rs48246560 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88656654 | CATACAATCAAATAA[A/G]TATACATTCTGGCCA | 257632 |
rs48266287 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88672153 | GGTTTCAAGTGCCCT[A/G]GAAAGATGAATTTGA | 257632 |
rs48289163 | snp | C/T | | | synonymous-codon | Nod2 | GRCm38.p3 | 8:88665268 | TGCTATGCCGGGCTT[C/T]ATTTGGCTCATCCGT | 257632 |
rs48307521 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nod2 | GRCm38.p3 | 8:88676270 | GAGAGAAAACAAATG[C/T]TGAGTGATTTCTCCA | 257632 |
rs48325442 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88669692 | CAGTTAGTGACTAGC[C/T]GATCAAGGTCAGCGC | 257632 |
rs48336567 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650012 | CTGTCAGGAGGACAG[C/T]TTCAAGCCCAGGTCT | 257632 |
rs48350454 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Nod2 | GRCm38.p3 | 8:88657169 | AATCCACCACAGCTA[C/T]CTTTTGCTGTTTTCT | 257632 |
rs48359423 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88675262 | CTAATCCATTGAGAA[C/T]GGCTGGCCAGTTGGG | 257632 |
rs48384076 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88662877 | TTTTAGGACTGTACA[A/T]TGTGGCCAGGAGGGT | 257632 |
rs48388447 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88656358 | TCTCTCTTCTATTTT[G/T]TAGACAATTTAGGAA | 257632 |
rs48396237 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88676513 | TCAAAGACAGCTGCA[C/T]CACCAAAACGCACCC | 257632 |
rs48436459 | snp | A/G | | | missense | Nod2 | GRCm38.p3 | 8:88665134 | TTGGCTGCATGCCAG[A/G]TCTCCGAGAGGGTAC | 257632 |
rs48457168 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88684084 | TATGTCCCCGAACAT[C/T]GCTGTTTATGAGTTA | 257632 |
rs48492251 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nod2 | Mm_Celera | 8:88679208 | GCCATCTCAGTTTTC[A/G]ATGCATTGCTAACCA | 257632 |
rs48557526 | snp | A/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685855 | GAGCCCCGTTCCCAG[A/T]GTCAGACATTTAAGC | 257632 |
rs48575014 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88656975 | AATGCTGGAATTTCT[A/G]GATGAATCCTCCAGT | 257632 |
rs48606370 | snp | C/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650800 | AGACTCAGTCCACGA[C/T]TTGGCCCCAGCTCAT | 257632 |
rs48618557 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88659211 | TCCTCTGACTGTGGT[A/G]TGGGGGATGGAATAG | 257632 |
rs48644532 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Nod2 | GRCm38.p3 | 8:88654315 | TCTGGGTTCAGTGTC[A/G]CGCTCGTGCTGCTTG | 257632 |
rs48686626 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88672668 | ATCTTCTGTGTCTTC[C/T]TGCCAGGGTGGGGAA | 257632 |
rs48707559 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88676522 | GCTGCATCACCAAAA[C/T]GCACCCCAGCATGGT | 257632 |
rs48744021 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Nod2 | Mm_Celera | 8:88662192 | AGAGGTCTCTAATAC[C/T]GACTGCAGCAGCACG | 257632 |
rs48744581 | snp | A/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662986 | AGCTCAGGTGGCAGT[A/C]GGCCGGGACATAGCC | 257632 |
rs48750955 | snp | A/G | | | synonymous-codon | Nod2 | GRCm38.p3 | 8:88665142 | ATGCCAGGTCTCCGA[A/G]AGGGTACTGCTCCAG | 257632 |
rs48752811 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nod2 | Mm_Celera | 8:88654614 | GCATTAATATCAAAA[A/G]TATCTAGACTGTCTA | 257632 |
rs48782568 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Nod2 | GRCm38.p3 | 8:88657286 | TATTACAGCAACTTG[A/C]TCTTGTTTTAGGGAA | 257632 |
rs48804122 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88656508 | CTTATGTATACTACA[G/T]AGTGAGTGAGTTTAA | 257632 |
rs48805532 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Nod2 | GRCm38.p3 | 8:88676957 | ACCATGCCACAGAAC[A/G]GTCACTTGTTCTTTG | 257632 |
rs48808431 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Nod2 | Mm_Celera | 8:88653576 | GAGCACATGTCAAGC[A/G]CTTCATCTGTTCCTT | 257632 |
rs48816549 | snp | C/T | | | synonymous-codon | Nod2 | Mm_Celera | 8:88664549 | TGCCACCGGGAACTT[C/T]TGCTGCAGAACAGGG | 257632 |
rs48817184 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88656451 | GCACATCTATAATTC[C/T]AGCTTCCTAGAAGGC | 257632 |
rs48869671 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88670266 | GATTTTGGATGGGGG[C/G]GGGGGGTCTCTATCT | 257632 |
rs48890209 | snp | C/G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685128 | GGAGGCAGAGGCAGG[C/G/T]GGATTTCTGAGTTCA | 257632 |
rs48892915 | snp | A/G | | | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88645647 | CCTCCAAGTTGTCCT[A/G]TGACCTCCACTCATG | 257632 |
rs48932596 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88679956 | TGCAGGGAGTTTAAT[A/G]GGTTGAATCATGCCC | 257632 |
rs49019879 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nod2 | Mm_Celera | 8:88654881 | taagactacatagtt[A/T]gagactccatcaaaa | 257632 |
rs49021304 | snp | A/G/T | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88648717 | AGGAAAGGGGTGGCA[A/G/T]CTGAGGTCTCTTGTA | 257632 |
rs49024987 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88681559 | GGAGGTCAACCCATT[C/T]TGACATCCTCCTCCA | 257632 |
rs49033188 | snp | C/G | 0.408163 | 0.193609 | missense | Nod2 | GRCm38.p3 | 8:88675481 | GGCAGCATGGGTGCC[C/G]AAGCCCTAGCACTGA | 257632 |
rs49044024 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nod2 | Mm_Celera | 8:88653816 | TGCTGTCATGTCGTG[C/T]TGAGTGGCTCTCTGT | 257632 |
rs49044759 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88677915 | AAGTGTTTTTCATTC[A/G]CAGAGGTGGAACTGT | 257632 |
rs49055106 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nod2 | GRCm38.p3 | 8:88670916 | CTCTGTGGAGGCTAA[A/G]GAGCTCCTGTCTTTT | 257632 |
rs49078356 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Nod2 | Mm_Celera | 8:88673774 | GTAATCTATTTGACA[C/G]TCACCTGTTGATATG | 257632 |
rs49097036 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88655089 | TGTCTTTGTTCCCTT[C/T]AGCTCTGGAGTCTTG | 257632 |
rs49098175 | snp | A/G | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88688146 | CCGGAGTCGGTGCCT[A/G]TGAACTGAACTCTGA | 257632 |
rs49104823 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88668057 | CTTTTAGTCCTGAGT[A/G]GTTACCATGTGTGGA | 257632 |
rs49124897 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650879 | GGCTGAGTACAGGGT[A/G]CAGGTGACATGCTTG | 257632 |
rs49176590 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88677824 | CGTATGTATGTCACC[G/T]CTGTAGAATTTGATT | 257632 |
rs49227888 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Nod2 | Mm_Celera | 8:88669990 | TGTTTCCAAGGTCTG[A/G]GATACTTGTGTCTAG | 257632 |
rs49233925 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88668068 | GAGTGGTTACCATGT[A/G]TGGATGTATGTCCCT | 257632 |
rs49259843 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88668263 | GCCTTGACGCAGGTT[C/T]CAAAGCAGGAAGGCC | 257632 |
rs49264769 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88671678 | TGGATCAGTTGTTTT[C/T]GTTCCCGTCTCTTTC | 257632 |
rs49271099 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Nod2 | GRCm38.p3 | 8:88678739 | AGGGATGGGAAATTA[A/T]ATTGCTCAGCGTTTC | 257632 |
rs49273753 | snp | C/T | 0.32 | 0.24 | intron-variant | Nod2 | GRCm38.p3 | 8:88659271 | CAGCTGTGCAGTTTC[C/T]GGGTAAGCCATGATG | 257632 |
rs49293406 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88678097 | CAGGAAGGGACATTT[A/G]AAGTAGTGGGGCACA | 257632 |
rs49324964 | snp | A/C/T | 0.486111 | 0.0821678 | intron-variant | Nod2 | GRCm38.p3 | 8:88678648 | AACAAATTGTCCTTA[A/C/T]GGCTTTAATAAGCCA | 257632 |
rs49328239 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88671755 | TGGAGTTAACGCACG[C/T]AACGAGCTGGTACAG | 257632 |
rs49331170 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88676408 | AGCCCAGGATGGATG[C/T]CACTGAACTCCAACT | 257632 |
rs49343034 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88672549 | TGACTCCTGCCCAGA[C/T]CTATTTGGAAAACCA | 257632 |
rs49356305 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88672003 | TTGGTGCCACTCTGC[A/G]AGAATTCATGAGGCT | 257632 |
rs49358699 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88665570 | GCTACTGTCAAGGCT[A/G]GACGTAGAAGCATAG | 257632 |
rs49369712 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88649127 | CACATGATGTTGAAT[A/G]GTGTCCAGTAACATT | 257632 |
rs49412699 | snp | G/T | | | missense | Nod2 | GRCm38.p3 | 8:88664376 | TCGTTCGCACAGAGT[G/T]GCAACTGAAGGGCTT | 257632 |
rs49422990 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nod2 | Mm_Celera | 8:88671062 | GAATCTGCGCTAACT[C/G]TCACAGCTGTGGTAC | 257632 |
rs49436024 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88649921 | CAGTGTGTTTAGCCT[A/G]GGGAGAGCAAGTCTG | 257632 |
rs49447087 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88678527 | ACCCAGTGAACTGGG[C/G]TTCAAACACAGCCAC | 257632 |
rs49457374 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88657853 | TCATTTAAACTCTGG[C/T]TTTGGGGGAATGGCA | 257632 |
rs49508144 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88680691 | GGCAATGGCTCTCCA[C/T]TTGCCTCATTTGGAT | 257632 |
rs49515807 | snp | C/T | | | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88646425 | GGTGGCCTCCAGGCT[C/T]CCTCATAACCTGTAG | 257632 |
rs49536848 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Nod2 | Mm_Celera | 8:88668155 | TAATTGGAGGTGTGC[A/T]CTTGTAAGGGATTAT | 257632 |
rs49541744 | snp | C/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650158 | GGGAATTTCCAGCTT[C/T]AATAGAAGACAGAGT | 257632 |
rs49558800 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662689 | AGGTCTCAGAGTTAG[C/T]CTTTCAGTCTGACTA | 257632 |
rs49590621 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685884 | GCAGAGGAAAGGAAC[C/T]GGTGGCCCTTCTTAG | 257632 |
rs49622061 | snp | C/T | | | utr-variant-3-prime | Nod2 | GRCm38.p3 | 8:88687893 | CAACAGGACTCAACT[C/T]CGACAACCAACATAA | 257632 |
rs49639833 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88655768 | TCCAGATGAAGAAAC[G/T]ACCTTATTGATACCC | 257632 |
rs49666468 | snp | A/T | | | utr-variant-3-prime | Nod2 | GRCm38.p3 | 8:88687230 | TGATGGAACGTGAGG[A/T]GTCGAGCTTCTCCAG | 257632 |
rs49668074 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Nod2 | GRCm38.p3 | 8:88654653 | AACTGGGATAACTTA[C/T]AGGCCAAAGAAGCAA | 257632 |
rs49675314 | snp | C/T | 0.32 | 0.24 | intron-variant | Nod2 | Mm_Celera | 8:88670392 | CTACTTTTAACTGAA[C/T]CCATGATGTCTTTTT | 257632 |
rs49726269 | snp | G/T | 0.5 | 0 | intron-variant | Nod2 | Mm_Celera | 8:88673484 | CCTTGAAACCAGAGA[G/T]TCACCTGCCTCTGCC | 257632 |
rs49748791 | snp | A/C | 0.32 | 0.24 | intron-variant | Nod2 | Mm_Celera | 8:88673232 | TTAGTTGCCTGTAAA[A/C]TCAGTGTGAGCCAGG | 257632 |
rs49757467 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88678859 | ACCTTCCCTAATTAC[A/G]TCAGTGCAAGTATTG | 257632 |
rs49787604 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685172 | GAGTTCCAGGACAGC[C/T]GAGGCTACACAGAGA | 257632 |
rs49800979 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88654990 | AGGAGTGAGCTGAGG[A/G]ATAGGACAGTGGGTA | 257632 |
rs49803184 | snp | C/G | 0.231111 | 0.249285 | missense | Nod2 | Mm_Celera | 8:88653173 | TGGGACACTCACTCC[C/G]TTCATCCAACCAGAG | 257632 |
rs49863852 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88671797 | CTTTATATAGTAAGC[C/T]GAGAGACTGAACGAT | 257632 |
rs49866960 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nod2 | Mm_Celera | 8:88682777 | GGAGGAGGATGTGGA[A/G]CCATGGgtgtgtgtg | 257632 |
rs49874986 | snp | C/G | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88654317 | TGGGTTCAGTGTCGC[C/G]CTCGTGCTGCTTGAG | 257632 |
rs49877137 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nod2 | Mm_Celera | 8:88653707 | GCAGGATACTGTTAA[C/T]CTCTGATGTTCAAGG | 257632 |
rs49889941 | snp | A/G | 0.489796 | 0.070696 | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88647040 | AACACCACCCAGCAC[A/G]GCCTTCTGGGAATGC | 257632 |
rs49890464 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88686406 | GTCATGGAGCCTTGC[C/T]CATTCTTTGGGCTGG | 257632 |
rs49920465 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685222 | AATGTATAGTGGTTT[A/G]GTTAGACAATTAAAA | 257632 |
rs49930960 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Nod2 | GRCm38.p3 | 8:88672641 | AGGTGCCAGCATGCT[A/G]TACCTTCCTTGATCT | 257632 |
rs49931525 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88677035 | GTAGGTGTAACACAC[A/T]GGTTTAGAGGGCAGT | 257632 |
rs49954674 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88673163 | TGAGATCCAAGATGT[A/G]GGAAGAGAGGGTAAC | 257632 |
rs49960334 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88668029 | GAGAATCCTGCCCTG[C/T]AGAAATCAGCTTCTT | 257632 |
rs49966429 | snp | C/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646254 | TTCAGTTTCTTCATC[C/T]GTAAGCCTGGGACAA | 257632 |
rs49988755 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88657734 | CTTCTTCAGATAAAA[A/G]GCCTCCTGCCTGTGG | 257632 |
rs49997989 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88669561 | GTGTAGACTCTTACC[C/T]TTTTGGGACCATAAG | 257632 |
rs50000383 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88654213 | GGTGAAATAAGTGAG[C/T]TGTTAGGAACATGTC | 257632 |
rs50017589 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88668025 | CTGTGAGAATCCTGC[C/T]CTGCAGAAATCAGCT | 257632 |
rs50032996 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88676172 | AGTGCTCACATGACA[C/T]CTGAAGCAGACCCTA | 257632 |
rs50044998 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88662987 | GCTCAGGTGGCAGTA[G/T]GCCGGGACATAGCCT | 257632 |
rs50077131 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nod2 | Mm_Celera | 8:88671404 | CTCAGGGCTACAAAG[A/G]CCAAAGCCACAGGTG | 257632 |
rs50096886 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Nod2 | Mm_Celera | 8:88677944 | GTTAGAGATTTTACC[A/T]CTTGCAGTTGCTGGT | 257632 |
rs50120784 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88665549 | CCGATTGGGCCTGTG[A/G]CAAATGCTACTGTCA | 257632 |
rs50121270 | snp | A/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88657468 | GTGACATCACTCACT[A/C]CTTGTATAAACCTTT | 257632 |
rs50129556 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662415 | TGAGTTGAGGCCAAA[C/T]GGGCTGGTGCTTTCC | 257632 |
rs50163432 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88656389 | TTGAGTGTCTAAAGC[G/T]TCCCTCATAGTTGAT | 257632 |
rs50171930 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nod2 | Mm_Celera | 8:88672233 | TTAGAGGAGACTAGA[C/T]CTAGCTATGCTGCAG | 257632 |
rs50181097 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88683261 | GGTTGTTGTCATTCG[A/G]ACAAGGCCTCTATAA | 257632 |
rs50195199 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88676910 | TTGGAGGAGGTCACT[A/G]TATATGGCCACCTAT | 257632 |
rs50216145 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88651281 | CAGCATCTTAGAATG[C/T]CCCAGATTTTGAAAG | 257632 |
rs50225280 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88657440 | ACATGCTAAACAATC[A/G]TTCTACCACTGTGTG | 257632 |
rs50239730 | snp | A/G | | | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88646162 | AAGCAGTGTGAGGCA[A/G]TGGTTAGCGCACAGT | 257632 |
rs50246316 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88657406 | CATTTCTGTGCTAGT[A/G]ATGGAACCCAGAGCA | 257632 |
rs50264909 | snp | A/G | 0.32 | 0.24 | intron-variant | Nod2 | Mm_Celera | 8:88676487 | GGCTTACTTACAGGA[A/G]CAGAAATGACTCAAA | 257632 |
rs50265778 | snp | C/T | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88688270 | GGACAAAACCAAGCC[C/T]TTCTTTCTGAGCAAG | 257632 |
rs50354736 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88647050 | AGCACGGCCTTCTGG[G/T]AATGCCTCCATTAAG | 257632 |
rs50401072 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88682274 | AACAGCAGGAGAATT[G/T]CAGTTCGGAGGTAGC | 257632 |
rs50412793 | snp | G/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650643 | TTCCCCATAACTTCC[G/T]GCTGTACCTCAGGCC | 257632 |
rs50421438 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nod2 | Mm_Celera | 8:88653751 | CTCCCCGATCACCCA[C/T]ATATCAATTAGAGAT | 257632 |
rs50431018 | snp | A/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685316 | AGACCCTTAGCACTT[A/C]TAAATTCTGGAGGTT | 257632 |
rs50480744 | snp | C/T | 0.32 | 0.24 | intron-variant | Nod2 | Mm_Celera | 8:88672456 | CGTGTACACTGAGGA[C/T]GGCTAAGACCAAGAA | 257632 |
rs50489708 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88681389 | TGAGACATTCATAAT[C/G]TAGGACAGCAAGAGT | 257632 |
rs50505202 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88672185 | TTGTATTTATTCTGG[A/T]AAGCTTGCCTTGTGG | 257632 |
rs50548092 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88663106 | GGACCAAGCATTCAG[A/G]CACACAAGCTAATGG | 257632 |
rs50565592 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88669870 | TTTAGGAAAGCTCTC[A/G]GATGACCTTGTGACC | 257632 |
rs50566006 | snp | A/C/T | 0.152778 | 0.230321 | intron-variant | Nod2 | Mm_Celera | 8:88659908 | ATGGGACTTGGTACA[A/C/T]CACCAGCCTTCCAGG | 257632 |
rs50575111 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nod2 | GRCm38.p3 | 8:88659237 | AATAGGCTGTAGGCA[A/G]GGATTGTGCAGAGAC | 257632 |
rs50586050 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88681463 | TGGACCACCTTTGCA[C/T]GGCTGTCCTGGGACT | 257632 |
rs50594472 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650465 | CAGGCTTCCTGCTGA[A/G]GCTTTTGGGATTTCC | 257632 |
rs50616127 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88657502 | CCTTCAAGTTACCAT[C/T]CCTTCTCTATTAATT | 257632 |
rs50627009 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685846 | CCTGGCTTGGAGCCC[C/T]GTTCCCAGAGTCAGA | 257632 |
rs50628465 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nod2 | Mm_Celera | 8:88648839 | TTGGCAGGGTTCATC[A/G]AGTTGTGAGGCTGAG | 257632 |
rs50630684 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88675905 | GTGTGTATGTGCTTA[A/G]TATAGACCCTGCCAT | 257632 |
rs50634206 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nod2 | Mm_Celera | 8:88673655 | CCTGCTCTGTAAGTC[C/T]GATCTCGTCTCTGGC | 257632 |
rs50657701 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88681319 | ATACCATCTCCTTCA[C/T]GAAGTACATAGCTTC | 257632 |
rs50677616 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88676402 | GATAGGAGCCCAGGA[C/T]GGATGCCACTGAACT | 257632 |
rs50678016 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88682359 | GGGTTGCAGCATCAC[A/G]AGGGTTGAGAACTGC | 257632 |
rs50682657 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685386 | TCCATAGAATTAAAA[A/G]CCAAAGACAGCCCTT | 257632 |
rs50683711 | snp | A/C | 0.5 | 0 | intron-variant | Nod2 | GRCm38.p3 | 8:88671550 | GCCTAGGTTTAGGGC[A/C]AGTCCACGGTGCTTT | 257632 |
rs50709008 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88663307 | CACTAAAGGGTGTCT[C/T]GGGCCACCCAACAGG | 257632 |
rs50731608 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88674552 | AAAAAGAGATGAAAG[G/T]CTGGCTTGTCCGGGA | 257632 |
rs50774596 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Nod2 | GRCm38.p3 | 8:88675448 | ACAATTCTGTCTAGC[C/T]TGGTAGGAAACAACA | 257632 |
rs50803677 | snp | C/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645748 | AAAACTGTTGGGTTT[C/G]AAACTGTTTCAAACA | 257632 |
rs50805370 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88671557 | TTTAGGGCCAGTCCA[C/T]GGTGCTTTCATCATG | 257632 |
rs50816767 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88657976 | ACAGTGAGTGGCTGG[C/G]TCATGCTTTGGAGTG | 257632 |
rs50830502 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88667799 | CTGTGACATGATGGG[A/T]CCAGAGGTCTGGGAG | 257632 |
rs50834263 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88672355 | GATTCCTCTTTTCTG[A/G]GTCCCTTCAGAATAG | 257632 |
rs50881513 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88683765 | TGCCAAGTGTTGGTT[A/G]GAGTCCAGGCTTCAC | 257632 |
rs50889572 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88657639 | AAACCTGTCTACAGT[A/G]ACTTTCACCGTAGAT | 257632 |
rs50900103 | snp | A/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88659242 | GCTGTAGGCAAGGAT[A/T]GTGCAGAGACTGGCA | 257632 |
rs50905799 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88685150 | CTGAGTTCAAGGTCT[A/T]CAAAGTGAGTTCCAG | 257632 |
rs50939130 | snp | A/C/G | 0.486111 | 0.0821678 | intron-variant | Nod2 | GRCm38.p3 | 8:88675649 | CCTGCAGACCCTGGT[A/C/G]CTTCACTGCTAATTC | 257632 |
rs50962885 | snp | A/G | | | synonymous-codon | Nod2 | GRCm38.p3 | 8:88664917 | CAGTGCTGACACATC[A/G]GTGGCCTCTCTCAAG | 257632 |
rs51021600 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nod2 | GRCm38.p3 | 8:88673154 | TGAGGATTGTGAGAT[C/T]CAAGATGTGGGAAGA | 257632 |
rs51029148 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nod2 | Mm_Celera | 8:88675228 | GCTGTGAGCTGAACC[C/T]ACCAGATAAGGACTT | 257632 |
rs51067974 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650991 | CTTTTCCCTGTCTGG[C/T]CAGCCCCAGGCTTCC | 257632 |
rs51072966 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88657666 | AGATGGTTAGACAAT[A/G]GTAGTGTATATAGTA | 257632 |
rs51104916 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88672018 | AAGAATTCATGAGGC[C/T]ACTGGGGTGGTCTCG | 257632 |
rs51112432 | snp | C/G | | | utr-variant-3-prime | Nod2 | GRCm38.p3 | 8:88686919 | CACTGACTTAAGAGA[C/G]TCATGAGCCGAGAGG | 257632 |
rs51121515 | snp | A/T | | | utr-variant-3-prime | Nod2 | GRCm38.p3 | 8:88687046 | TGCCCCGTGGGAGGA[A/T]GATGGAGGAGGAGGA | 257632 |
rs51135726 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88671213 | CCAAGTACTTAATGC[C/T]TCTCTCTTTAGTTGC | 257632 |
rs51139055 | snp | A/G | | | utr-variant-5-prime | Nod2 | GRCm38.p3 | 8:88647350 | GGAGTAGATCACTGA[A/G]GGAGTCCTAGTGTGG | 257632 |
rs51165187 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nod2 | Mm_Celera | 8:88676808 | TTTAAAGAGCTTTCC[C/T]GTAGGATGGAATGTT | 257632 |
rs51171657 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88679775 | ACAGACTAAAGTATG[A/G]ATTTCACCACTGGTG | 257632 |
rs51172310 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nod2 | Mm_Celera | 8:88669548 | TGCCTCCCTGCTAGT[A/G]TAGACTCTTACCCTT | 257632 |
rs51185603 | snp | C/T | | | utr-variant-3-prime | Nod2 | GRCm38.p3 | 8:88687838 | ACTCACTCTCTAAGG[C/T]CATCCCACTCTGATA | 257632 |
rs51194824 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Nod2 | Mm_Celera | 8:88668352 | ATTAATCACCTCAGG[C/G]ATTATGTTAGTAAGA | 257632 |
rs51214579 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88656867 | AATCCAGAAACTTGC[A/G]TCTTGGTGCTTGAGA | 257632 |
rs51216025 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88672810 | GAATGTGGGGCTTTC[A/C]CAGATTTAGGGGCAG | 257632 |
rs51230609 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88675733 | CCGTAATGGTGAAGA[C/T]CACAAACTCTGGAAT | 257632 |
rs51251857 | snp | G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88684105 | TTATGAGTTACTTCC[G/T]GTCAGTGAGGTGCTG | 257632 |
rs51269863 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nod2 | Mm_Celera | 8:88676412 | CAGGATGGATGCCAC[C/T]GAACTCCAACTTGGA | 257632 |
rs51299316 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685854 | GGAGCCCCGTTCCCA[A/G]AGTCAGACATTTAAG | 257632 |
rs51307513 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88657822 | AAGGTAACCTTGGCA[C/T]ATATTTTACACACAG | 257632 |
rs51317776 | snp | C/G | | | missense | Nod2 | GRCm38.p3 | 8:88664377 | CGTTCGCACAGAGTT[C/G]CAACTGAAGGGCTTC | 257632 |
rs51325547 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88675916 | CTTAGTATAGACCCT[A/G]CCATATGTGTACGTG | 257632 |
rs51327670 | snp | A/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88657544 | TCCCATTTTGACACT[A/T]TCTTTGGGCATAGGT | 257632 |
rs51338274 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650843 | TGTCATCTGCCTCTT[C/T]CCCATCCTTGGCTCC | 257632 |
rs51340019 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685229 | AGTGGTTTAGTTAGA[C/T]AATTAAAACAAGAGC | 257632 |
rs51345327 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658958 | AGCACACTGGGCATG[C/T]TCATTAAATGAGAGG | 257632 |
rs51351124 | snp | C/T | | | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88646228 | TGACAGGCTAGTGAA[C/T]TTTTTTGTGCTTCAG | 257632 |
rs51368738 | snp | C/T | 0.32 | 0.24 | intron-variant | Nod2 | Mm_Celera | 8:88652736 | TTTGATATCCCAGGG[C/T]TTCACTTTGGGGACA | 257632 |
rs51369260 | snp | A/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88675652 | GCAGACCCTGGTGCT[A/T]CACTGCTAATTCTTT | 257632 |
rs51375120 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651174 | GGAGACCTAGCCTGC[A/G]GTGTGGGCCTGCTGT | 257632 |
rs51395058 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nod2 | Mm_Celera | 8:88673051 | ACTGGGCTATCCTGG[A/G]AAGTACCTTCTGCTT | 257632 |
rs51395556 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88667823 | CTGGGAGGCTGTGGG[C/T]CTGTCTGTTTTCAGA | 257632 |
rs51407849 | snp | C/T | | | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88646233 | GGCTAGTGAATTTTT[C/T]TGTGCTTCAGTTTCT | 257632 |
rs51414345 | snp | C/G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88672441 | GGAGGGTTATGCTGG[C/G/T]GTGTACACTGAGGAT | 257632 |
rs51416929 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88654625 | AAAAGTATCTAGACT[A/G]TCTAAGAAAAGAAAC | 257632 |
rs51419994 | snp | A/G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88652151 | AGGGTATGTGTGTGT[A/G/T]TGTGTGTGTTGCTAT | 257632 |
rs51420212 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88676103 | CTACCTCAGAAGTCA[A/G]AGATCACATCAGATG | 257632 |
rs51421243 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88655797 | CCTATCCTTCACATG[A/T]AACCAGTAGAGGCAA | 257632 |
rs51421492 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651315 | GTCTTTCTTCCGCTT[C/T]CTCCTTGCCTGTGCT | 257632 |
rs51523127 | snp | A/G/T | 0.132653 | 0.220748 | intron-variant | Nod2 | GRCm38.p3 | 8:88673662 | TGTAAGTCTGATCTC[A/G/T]TCTCTGGCTTCCCAA | 257632 |
rs51570727 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nod2 | GRCm38.p3 | 8:88677143 | ACTCCCTTTTGCAGA[A/G]TGGGCCTAAAATCCA | 257632 |
rs51608244 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685668 | TCTGGGATCCTATTT[C/T]CTCTGTCCCCTGCTT | 257632 |
rs51637754 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Nod2 | GRCm38.p3 | 8:88677417 | TGTCTTCAGCAATAG[A/G]GTCGTACTGTCTGCT | 257632 |
rs51650089 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88653569 | ATCCCAAGAGCACAT[A/G]TCAAGCGCTTCATCT | 257632 |
rs51657741 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88676165 | GCCACCAAGTGCTCA[C/T]ATGACACCTGAAGCA | 257632 |
rs51673536 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon | Nod2 | Mm_Celera | 8:88674978 | CGACCACCAGAACCT[A/G]AAGTGGCTCAGGTAA | 257632 |
rs51711548 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88648808 | AACAGATAAGGCTCC[G/T]GCTCTGACTTAAGGT | 257632 |
rs51732438 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88672447 | TTATGCTGGCGTGTA[C/T]ACTGAGGATGGCTAA | 257632 |
rs51766474 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88678826 | GCCAGGCTCAGACAG[A/G]CTCTTGCATTATTTA | 257632 |
rs51789877 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nod2 | Mm_Celera | 8:88672111 | AGATGGTCATGCCTA[C/T]CCTATAAGATGGTTG | 257632 |
rs51801918 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88672336 | TGGTGTTGCTGAAGA[C/T]TCTGATTCCTCTTTT | 257632 |
rs51833082 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88675917 | TTAGTATAGACCCTG[C/T]CATATGTGTACGTGT | 257632 |
rs51839341 | snp | A/G | | | utr-variant-3-prime | Nod2 | GRCm38.p3 | 8:88686777 | CAGAATCCCTCTGCT[A/G]CGCAGGGCTGGTTTG | 257632 |
rs51849758 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nod2 | Mm_Celera | 8:88649157 | TTCAGTCATCGTTAT[C/T]TCACAGTTGGGAATT | 257632 |
rs51861364 | snp | A/C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88663070 | AGGTGCTACCTCTAC[A/C/T]GAGGCAGTACTATTA | 257632 |
rs51873078 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88657528 | TAATTTGTCTCTGAT[C/T]TCCCATTTTGACACT | 257632 |
rs51875090 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88654796 | TGGATGGGCAAAGAC[C/T]CCATCCCAAGAAAGA | 257632 |
rs51884543 | snp | G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685886 | AGAGGAAAGGAACCG[G/T]TGGCCCTTCTTAGGT | 257632 |
rs51889636 | snp | A/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685664 | CAACTCTGGGATCCT[A/T]TTTTCTCTGTCCCCT | 257632 |
rs51921037 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88673759 | ATTGGGTGGCTTTAC[A/G]TAATCTATTTGACAG | 257632 |
rs51955820 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88669462 | GAGTTTAGAGTCTTG[C/T]CACATGGAGTTCACT | 257632 |
rs51961015 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88663483 | TCAAAGTTCCCGGCT[A/G]TATTCCTGCTTTGCA | 257632 |
rs51961035 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88678805 | CCATGTCCCATGGCC[G/T]CACAAGCCAGGCTCA | 257632 |
rs51993373 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Nod2 | GRCm38.p3 | 8:88678142 | GTCTTACAAGGATCT[A/T]AGCCTGCTTAAAGCC | 257632 |
rs52009211 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88657891 | TCTAGTTGTGCCTGG[A/G]TTCTCCCAGTCCTGG | 257632 |
rs52023377 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88667637 | TGGGGCTTCAGCTAA[C/T]TCACACTGATCTCAA | 257632 |
rs52033843 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88671750 | CAGGATGGAGTTAAC[A/G]CACGCAACGAGCTGG | 257632 |
rs52052976 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nod2 | GRCm38.p3 | 8:88654233 | AGGAACATGTCAGGG[C/T]GAGGATGAGCAAGTT | 257632 |
rs52061091 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nod2 | Mm_Celera | 8:88671284 | CCTTTTATGATTTGC[A/G]AAGCAACAGTGAAGA | 257632 |
rs52152127 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88655983 | AGCATACTTTTGTCA[A/G]GAAACAGAAGCATTA | 257632 |
rs52193810 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Nod2 | Mm_Celera | 8:88655880 | TATGCCTTTTGCAAG[A/T]AATTTCCAAAAAGTG | 257632 |
rs52229482 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88678976 | CAATTTTTTCTTTTT[C/T]TTTTCTTTTTTTTTT | 257632 |
rs52274342 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88659756 | GTGTTTGTGTGTGCA[C/T]GCACGCGCACATACT | 257632 |
rs52282235 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88668507 | GTGTGTGTGTGTGTG[C/T]GCGCGCGTGCGTGCT | 257632 |
rs52296200 | snp | C/T | | | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88646599 | tctctcttctccctc[C/T]ccccaccccacattg | 257632 |
rs52352290 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88669564 | TAGACTCTTACCCTT[C/T]TGGGACCATAAGGCA | 257632 |
rs52381185 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88668505 | GTGTGTGTGTGTGTG[C/T]GTGCGCGCGTGCGTG | 257632 |
rs52459062 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88656005 | GAAGCATTATTGTTT[C/T]TTCTTAGATGGAAGC | 257632 |
rs52517123 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88678981 | TTTTCTTTTTCTTTT[C/T]TTTTTTTTTTTTTAA | 257632 |
rs52623468 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Nod2 | GRCm38.p3 | 8:88683743 | TTTCTTTTTCCAGTG[A/T]CTTCTCTGCCAAGTG | 257632 |
rs52630693 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nod2 | Mm_Celera | 8:88671173 | AATTTGAATTGCTTT[C/T]CTACCCAAGATTGAC | 257632 |
rs52633805 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Nod2 | Mm_Celera | 8:88668527 | GCGTGCGTGCTCTCG[A/C]GAGTGCATGTGCATA | 257632 |
rs107886113 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88676159 | GAACGAGCCACCAAG[C/T]GCTCACATGACACCT | 257632 |
rs108246188 | snp | G/T | | | missense | Nod2 | Mm_Celera | 8:88664565 | TGCTGCAGAACAGGG[G/T]CTTCCCAACAACCAG | 257632 |
rs108328192 | snp | C/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88672826 | CAGATTTAGGGGCAG[C/G]TGAGCACTTCACCCG | 257632 |
rs108812715 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88676142 | TGGAGTTTGGGATCA[C/T]TGAACGAGCCACCAA | 257632 |
rs211791646 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88657892 | CTAGTTGTGCCTGGA[A/T]TCTCCCAGTCCTGGG | 257632 |
rs211816409 | in-del | -/TC | | | intron-variant | Nod2 | Mm_Celera | 8:88656932 | TGTTGTTCCTTTTCT[-/TC]TCTCTCTATGGAATT | 257632 |
rs211844813 | in-del | -/CCTGCG | | | intron-variant | Nod2 | Mm_Celera | 8:88675639 | AGTCGTGCGCCTGCA[-/CCTGCG]GACCCTGGTGCTTCA | 257632 |
rs211966680 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88685584 | TCAGGAGGCTAGAGT[C/G]TGGGCAAGCTCCTGT | 257632 |
rs212042203 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88677377 | AGCTTAATTTCTCCA[C/T]GTTCTGTCAAGCATG | 257632 |
rs212219848 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88673653 | GACCTGCTCTGTAAG[C/T]CTGATCTCGTCTCTG | 257632 |
rs212225323 | in-del | -/CCACCCACCTAC | | | intron-variant | Nod2 | Mm_Celera | 8:88658160 | TGTTCATCTGTCCAT[-/CCACCCACCTAC]CCACCCACCCACCCA | 257632 |
rs212257359 | in-del | -/ATCCATCCATCCATCCATCCATCCATCCATCTATCCATCTGTCCATTCCATCT | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658403 | CCCACCCACCTGTCC[lengthTooLong]ATCCATCCATCCATC | 257632 |
rs212418115 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88673893 | TCCATATCCAATCTA[A/C]TGTATTGGTTAGCTC | 257632 |
rs212507019 | snp | C/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645346 | CACAGTGAGATTCTC[C/T]TTGCAGAAGCGCCTT | 257632 |
rs212697504 | in-del | -/A | | | intron-variant, downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88684543 | GGTAAGGGCCCTGGG[-/A]GGGAACTTCTGTGCC | 257632 |
rs212734100 | in-del | -/ATCT | | | intron-variant | Nod2 | Mm_Celera | 8:88658216 | ACCCATCTATCCCAC[-/ATCT]ATCTATCCATCCATC | 257632 |
rs212761963 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651350 | CGCTTTCCTTTTCTC[C/T]GGGTGTACTGGCTGG | 257632 |
rs212764593 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88667257 | GAGCATGAATTTGGC[C/T]AGGAAAATTAATGAA | 257632 |
rs212775739 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88652181 | TCAATGAGTGGCATA[A/C]CAATGGGCTCTGAAC | 257632 |
rs212836874 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88652765 | CAGTGCCTGAGAACA[C/T]CTGGCTCACTTGGAG | 257632 |
rs212900464 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88659766 | GTGCATGCACGCGCA[A/C]ATACTTATGACACAT | 257632 |
rs212946524 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88661467 | ATTCACTGTGTAGAT[A/G]CCACTGTGGCCCTTG | 257632 |
rs213016576 | snp | C/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645961 | AGACATCTGCATGCT[C/T]GTTCTTCTTATCTCT | 257632 |
rs213022380 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88654560 | AGGGAGTCTCTAAAG[A/G]GTTTGAGGAAGGAAG | 257632 |
rs213088473 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88654105 | GCCTGTGAAGCATGG[A/G]AAATGGTAACATTCT | 257632 |
rs213088751 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88662012 | AGGCTATCGTGCCAG[C/T]ACTAGGTTTGTTTGG | 257632 |
rs213094985 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88674690 | ACACCCCTGTGTGAT[A/C]CCTGAGGTGGATTCC | 257632 |
rs213150320 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88652186 | GAGTGGCATACCAAT[A/G]GGCTCTGAACCAACT | 257632 |
rs213161459 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88682399 | GAGTGGCAGGTCTCA[A/G]CAAGCAACTCCCGGA | 257632 |
rs213186925 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650876 | CTGGGCTGAGTACAG[A/G]GTACAGGTGACATGC | 257632 |
rs213208685 | in-del | -/G | | | intron-variant | Nod2 | Mm_Celera | 8:88666300 | CGTTTCCACTGCTCT[-/G]GGGGAATCCTTGAGG | 257632 |
rs213217718 | snp | A/G | | | intron-variant, downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88684695 | CTGTGAAGGAAATCT[A/G]TATCTCCCAGTAGGG | 257632 |
rs213220272 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88667269 | GGCTAGGAAAATTAA[C/T]GAACATGATCTGTAC | 257632 |
rs213247802 | in-del | -/ATGTATATT | | | intron-variant | Nod2 | Mm_Celera | 8:88683580 | TATCTATATCTATAC[-/ATGTATATT]ATTTATATTATTTAT | 257632 |
rs213257867 | in-del | -/GGGGGG | | | intron-variant | Nod2 | Mm_Celera | 8:88675538 | AACTCTGGTGAGTTA[-/GGGGGG]TGGGGGGTTTGCCTA | 257632 |
rs213342242 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88651521 | CTCTGGGCTGGTTGT[A/C]TTGGGTTCTATAAGA | 257632 |
rs213394936 | in-del | -/TGG | | | intron-variant | Nod2 | Mm_Celera | 8:88648024 | TCATCTCTGCCCTCC[-/TGG]TGAAGACCAAAGAGT | 257632 |
rs213572569 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88667136 | TCTGAGGTAAGAAGG[C/T]GCTTTTCCTCTGCCC | 257632 |
rs213631937 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88672617 | CACTACTACACCCCA[A/G]GAGAGGCCAGGTGCC | 257632 |
rs213679931 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88659044 | AGTCAAGAAGAGATG[C/T]AGTCTGGGTTTACAT | 257632 |
rs213750529 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88662751 | GGGGGGCCGGGGGGG[C/T]GTCTGGGAATCAGAT | 257632 |
rs213762129 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88674599 | TGGGTAGTCCCTGAG[A/G]ATAGTTAGAGACTTG | 257632 |
rs213970176 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88652070 | GAGCTCCTGAGGATT[A/G]TGGCAGAGGGGCTGC | 257632 |
rs214043266 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88660829 | CTCCCCCTTCCTTGC[G/T]CCCCAAACCACATGA | 257632 |
rs214088659 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88679432 | ATTCTTCCCGTAGAC[A/C]CTCCTAATTGTGAGG | 257632 |
rs214095600 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88680445 | TAAGTGTATGGCTTC[C/T]CACAACAGAACAAGG | 257632 |
rs214117987 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88670984 | CTCCCTGCCCGCACC[A/G]CCCTCCGAGTGCCCT | 257632 |
rs214286157 | in-del | -/GGA | | | intron-variant | Nod2 | Mm_Celera | 8:88672426 | GGGTAGGGATTGGGG[-/GGA]GGGTTATGCTGGCGT | 257632 |
rs214342873 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88661304 | GAAGAAACCTAATAT[A/G]GACTTCTGGTCCATG | 257632 |
rs214402405 | snp | A/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646899 | CGCTGGCGAATTCCG[A/T]TTAGGATGGTGGCAG | 257632 |
rs214409132 | in-del | -/A | | | intron-variant, downstream-variant-500B | Nod2 | Mm_Celera | 8:88684905 | GAGGGAGAGGGAGAG[-/A]AGGAAGAAGAAGAAG | 257632 |
rs214438942 | in-del | -/GGGGG | | | intron-variant | Nod2 | Mm_Celera | 8:88669146 | AATGATACTACTGTT[-/GGGGG]GGGGGGGTACACAGA | 257632 |
rs214588806 | in-del | -/AA | | | intron-variant | Nod2 | Mm_Celera | 8:88685199 | AGAAACCCTGTCTTG[-/AA]AAAAAAAAATGTATA | 257632 |
rs214699060 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88647460 | TGATCGGGGTGGGTG[A/G]ATATGTGGAAAGGAG | 257632 |
rs214712565 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88684019 | TTACAAGGCAAGGAG[C/T]AAAAGTTTCCATTGT | 257632 |
rs214726485 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88663204 | CCAAATGGCTTGCCA[A/G]GCAAATGGTGGGCCT | 257632 |
rs214769920 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88654537 | AGTGTTCAGCAGTGT[A/G]TCCAGGGAGGGAGTC | 257632 |
rs214790101 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88662747 | ACATGGGGGGCCGGG[C/G]GGGCGTCTGGGAATC | 257632 |
rs214832571 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88656528 | AGTGAGTTTAAGGAT[A/G]GTCTAGTCAGTTTGG | 257632 |
rs214892171 | snp | C/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646833 | CTCTCTCAAATGAGA[C/G]TTCATGTACAAGTCT | 257632 |
rs214977910 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88653921 | GAATTTAATCGTGTA[G/T]CCCACTGTGTGCCAA | 257632 |
rs214983140 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88649413 | TGGGTGTGGGAGGGG[A/G]TGAAGGAGATGGGGT | 257632 |
rs215099133 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88678963 | ATAGATTTTTTTCAA[-/T]TTTTTTCTTTTTCTT | 257632 |
rs215134205 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88653742 | GGGGGAGAGCTCCCC[A/G]ATCACCCATATATCA | 257632 |
rs215138173 | snp | C/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646059 | GAACCTGCTCTAGAG[C/T]GGCTCCCAAATAAAC | 257632 |
rs215323325 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88648328 | AAACACATCCTCAGC[C/T]CATGCAGACCCCATC | 257632 |
rs215486246 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88675161 | TTGGCGGTGAATTTG[A/G]AGGTGACTTTCCCTC | 257632 |
rs215511090 | snp | C/T | | | missense | Nod2 | Mm_Celera | 8:88670445 | TCAGACCGAGGTGCC[C/T]GCACGCTGGTTGAGT | 257632 |
rs215565243 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88669767 | CAAGGATTACTTACA[C/T]GTGCCAGTGGAGGGC | 257632 |
rs215571354 | in-del | -/TATATTATT | | | intron-variant | Nod2 | Mm_Celera | 8:88683583 | CTATATCTATACATG[-/TATATTATT]TATATTATTTATATC | 257632 |
rs215597807 | in-del | -/G/GGG/GGGGG/GGGGGG/GGGGGGG | | | intron-variant | Nod2 | Mm_Celera | 8:88675539 | ACTCTGGTGAGTTAT[-/G/GGG/GGGGG/GGGGGG/GGGGGGG]GGGGGGTTTGCCTAG | 257632 |
rs215603286 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88678010 | AGCACCCAAACCCTA[C/T]GAGAACCATTTGTCA | 257632 |
rs215710781 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88672117 | TCATGCCTACCCTAT[A/C]AGATGGTTGTGAGCC | 257632 |
rs215741034 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661280 | CCAGTCTTGTTCTCA[C/T]ATAACTGGGAAGAAA | 257632 |
rs215890765 | snp | G/T | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650744 | GGACCCAGGCAGGGG[G/T]GCTGGAGTAGCACCC | 257632 |
rs215912220 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88667750 | ATTTTTAAATGGTCC[C/T]TTTTTTTTAATGATT | 257632 |
rs215931652 | in-del | -/AGGTAG | | | intron-variant | Nod2 | Mm_Celera | 8:88648600 | TGTGTGTGTGTGTGT[-/AGGTAG]GTAGGTAGGGAGGGA | 257632 |
rs215950679 | in-del | -/CCCCCACCCCCG | | | cds-indel | Nod2 | GRCm38.p3 | 8:88687604 | CCACCCCCACCCCCA[-/CCCCCACCCCCG]CCCCCATTACTATGT | 257632 |
rs215966209 | in-del | -/A | | | intron-variant | Nod2 | Mm_Celera | 8:88648551 | TGACTATCTAGGGGG[-/A]GCTAGAGAAAGCCCC | 257632 |
rs216012915 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88660768 | ATCTGAAGCCTAGCA[C/G]CAACCTGACAGCAGT | 257632 |
rs216069456 | in-del | -/GGAGGCCTG | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88649654 | TCTCTCCCGTCTGCT[-/GGAGGCCTG]GGGGCACTGCAAAGG | 257632 |
rs216092521 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88683768 | CAAGTGTTGGTTGGA[A/G]TCCAGGCTTCACAGG | 257632 |
rs216142611 | in-del | -/G | | | intron-variant | Nod2 | Mm_Celera | 8:88671352 | CTGCCTTTGGAATGA[-/G]GGAGGCCATTTTAAA | 257632 |
rs216299875 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650345 | GTTTATTGGAGACAC[A/C]TCACACCACCAGGGT | 257632 |
rs216331086 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88686179 | AAAATAATTGCATAG[C/T]CCCAAGATATGTCCC | 257632 |
rs216362639 | snp | C/T | | | synonymous-codon | Nod2 | Mm_Celera | 8:88664335 | GACCAGCCGTCCGGA[C/T]GCTGTGTCAGCGCTC | 257632 |
rs216486487 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88685033 | CCAGGAGTATTTATT[C/T]TGAAACTTTGGTGTT | 257632 |
rs216505319 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88648508 | TCACCACTGAGCAAA[A/G]TCTTAAGGAGGGGAT | 257632 |
rs216582927 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88662077 | GGCATTCTAAGTCAT[G/T]GCGTTGGAAAGGGGC | 257632 |
rs216609022 | in-del | -/TGG | | | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88646572 | TCTCTCTCTCTCTCT[-/TGG]CTCTCTCTCTCTCTC | 257632 |
rs216673750 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88685452 | TCTAGGCTCCTTGGT[C/T]CTCGTGCAGAAAGCA | 257632 |
rs216732020 | snp | C/G | | | synonymous-codon | Nod2 | Mm_Celera | 8:88686672 | GGAAATCCAAACACT[C/G]AGCTCCAGGGACGCC | 257632 |
rs216777808 | in-del | -/TGG | | | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88646576 | TCTCTCTCTCTCTCT[-/TGG]CTCTCTCTCTCTCTT | 257632 |
rs216858798 | in-del | -/G | | | intron-variant | Nod2 | Mm_Celera | 8:88663499 | TATTCCTGCTTTGCA[-/G]GGGAAGAACCAGGTT | 257632 |
rs216919718 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88663386 | CTTCAGGAGTGCATA[A/C]TAAGAATGACTGTGG | 257632 |
rs216978719 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650973 | GTAGCTTCGCTGCCT[-/C]GGCTTTTCCCTGTCT | 257632 |
rs216985664 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88657281 | TTCTTTATTACAGCA[A/C]CTTGATCTTGTTTTA | 257632 |
rs216985681 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88649561 | GAGAGGAGTTAGTTA[A/G]TGCTCCAGGGAGATC | 257632 |
rs217079366 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88657432 | GAGCATTCACATGCT[A/T]AACAATCATTCTACC | 257632 |
rs217172630 | snp | G/T | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88651500 | GCCCCGTGTGGGTGG[G/T]ACCATCTCTGGGCTG | 257632 |
rs217182449 | in-del | -/ACACACACACACAC | | | intron-variant | Nod2 | Mm_Celera | 8:88683647 | AGGGAAACAGGATGG[-/ACACACACACACAC]ACACACACATACACA | 257632 |
rs217227352 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88678750 | ATTAAATTGCTCAGC[A/G]TTTCTGCCTCCACAG | 257632 |
rs217398080 | snp | C/T | | | utr-variant-3-prime | Nod2 | GRCm38.p3 | 8:88687579 | CAAGCACTGGATGAG[C/T]TCAAGCAGGCCACCC | 257632 |
rs217472851 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88674000 | GGGCTCAGTTCACGA[C/T]TGTCTGGCCCCGTAA | 257632 |
rs217482783 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88681256 | CCTTGTGTACCCATG[A/G]CTGCCGTGTGTCACT | 257632 |
rs217516470 | snp | G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88680223 | GAGTCTCCCTGCAGA[G/T]AATGTTTCAATCTCA | 257632 |
rs217617477 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88674503 | AGAAGGTAAAGGGTG[C/T]GGACATGATAGAAAC | 257632 |
rs217699487 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88652003 | ATCTTAGTGCCTAAA[A/G]CCTCTGATGGTCCCT | 257632 |
rs217737060 | in-del | -/GCGCGC | | | intron-variant | Nod2 | Mm_Celera | 8:88668508 | TGTGTGTGTGTGTGT[-/GCGCGC]GTGCGTGCTCTCGCG | 257632 |
rs217886665 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88651227 | CAGGAAAGACCTGGG[A/C]TCCCCAGGCCATTTC | 257632 |
rs217956680 | in-del | -/A | | | intron-variant | Nod2 | Mm_Celera | 8:88661682 | ATGAGACCCTCTCTC[-/A]AAAAAAAAAAGTAAA | 257632 |
rs217979294 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88647556 | GTCACAAGTCCCATC[A/G]CGGGGACGCTGTTAA | 257632 |
rs218016175 | snp | A/G | | | missense | Nod2 | Mm_Celera | 8:88664651 | GACTCCTCCCCACTC[A/G]GTCTGGGACCTGGAC | 257632 |
rs218047583 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88648180 | CTCTCTCCCACCCAG[G/T]TCAGCATTGTAGGGT | 257632 |
rs218080044 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88658113 | AAGTCTTCTACCATC[C/T]ATCCATGTGTCCATC | 257632 |
rs218102913 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88663479 | CATATCAAAGTTCCC[A/G]GCTATATTCCTGCTT | 257632 |
rs218132903 | snp | A/G | | | synonymous-codon | Nod2 | Mm_Celera | 8:88665457 | GGATTACAACTCTGT[A/G]GGAGATGTTGGAGTG | 257632 |
rs218156511 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88663053 | GAGATTCTGTATCCT[A/T]AAGGTGCTACCTCTA | 257632 |
rs218338506 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88679825 | GTTACTTGTAGGAAT[A/G]TGGGTGAGGGGTTAC | 257632 |
rs218416743 | snp | C/T | | | downstream-variant-500B | Nod2 | Mm_Celera | 8:88688705 | GCCTTCCTTAGTTCC[C/T]TAGTTCTCTCCTGGT | 257632 |
rs218435608 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88685816 | GTGCTGGGATTGCAG[C/G]TGTGCACCGCCATGC | 257632 |
rs218478103 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88680583 | GCAAAGACTGATCCA[C/T]AGATTGGTACTAGGA | 257632 |
rs218521078 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88652301 | TGTACAGAGGCAGGG[C/T]TGCGGGGATAACCAA | 257632 |
rs218547777 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88659216 | TGACTGTGGTGTGGG[A/G]GATGGAATAGGCTGT | 257632 |
rs218608094 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88663397 | CATAATAAGAATGAC[A/T]GTGGCTAATGTCCTT | 257632 |
rs218613030 | snp | C/T | | | missense | Nod2 | Mm_Celera | 8:88664076 | AATGCGTGGCCAAAC[C/T]GCTGTCCCTGAGGAC | 257632 |
rs218681288 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88666017 | AGCAATTCCTCAATT[A/G]AGACTCCCTTGTCCC | 257632 |
rs218842204 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88676724 | GGGTGGGAATGGGGG[-/T]GATGGAGGAGAGGAG | 257632 |
rs218916334 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88672321 | CTCCTGCAGTATCCT[C/T]GGTGTTGCTGAAGAC | 257632 |
rs218976825 | in-del | -/AG | | | intron-variant | Nod2 | Mm_Celera | 8:88648598 | TGTGTGTGTGTGTGT[-/AG]GTGTAGGTAGGGAGG | 257632 |
rs219158831 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88652608 | AGGAGGGAACTGACC[C/T]GCAGAAGCTGGCTTC | 257632 |
rs219216125 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88660230 | GCTTGATGCCAGGAG[C/T]GTTTCAGAAAATTTT | 257632 |
rs219303656 | in-del | -/C | | | intron-variant | Nod2 | Mm_Celera | 8:88668862 | CTCTCTTTCAGCTGT[-/C]CCTATTTCAGCGTTG | 257632 |
rs219326580 | in-del | -/GCCT | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646404 | TACCAAAGCACCAAA[-/GCCT]GTGGTGGCCTCCAGG | 257632 |
rs219483031 | snp | A/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645618 | GACCCCACATGGTGA[A/G]AAGAGAACTGAGTCC | 257632 |
rs219499642 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88667389 | GGCCAAGCCTTTTTT[G/T]TTTCAAGACACAGTT | 257632 |
rs219556993 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650792 | CACAGTGGAGACTCA[A/G]TCCACGATTTGGCCC | 257632 |
rs219667277 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88667565 | AACCTCAGAAGACCA[C/T]ATATACTGGCCTGGA | 257632 |
rs219714119 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88674870 | GAAAGCACATGAACA[C/T]GTACATGCCTAAAAC | 257632 |
rs219743344 | in-del | -/GGA | | | intron-variant | Nod2 | Mm_Celera | 8:88670355 | GAGGGTCTCCTTGGG[-/GGA]GGGGGGGTTGTCTCA | 257632 |
rs219761396 | in-del | -/CCTCTC | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646806 | GGTCAATTATTCTCT[-/CCTCTC]CCTCTCCCTTTCTCT | 257632 |
rs219767382 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650434 | GCAAGTTCTTCTGGG[C/T]GCTGGCCTGCCACCT | 257632 |
rs219768398 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88673732 | TAAGAAGAGTTGTAT[A/C]GCCTTCCCCTGATTG | 257632 |
rs219867575 | in-del | -/C | | | intron-variant | Nod2 | Mm_Celera | 8:88660674 | TCTGGTTAACACAGA[-/C]CCCCTGGTTAAAGAG | 257632 |
rs219871345 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88669453 | GGCTTTTGAGAGTTT[A/T]GAGTCTTGTCACATG | 257632 |
rs220016300 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88656355 | TATTCTCTCTTCTAT[A/T]TTGTAGACAATTTAG | 257632 |
rs220031925 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88683669 | ACATACACACACACa[C/G]agagagagagaggga | 257632 |
rs220139359 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88649891 | AGCCTGGTAGAGAAG[A/G]CAAGGATGACAAAGC | 257632 |
rs220257167 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88676688 | ATGTGAGAGGGACTC[A/C]CGGCTTTTGTTGTTT | 257632 |
rs220263033 | in-del | -/GCTGTGGC | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88687743 | AACTGAACGCCTGTT[-/GCTGTGGC]GCTGTGGATCCACAT | 257632 |
rs220277457 | in-del | -/G | | | intron-variant | Nod2 | Mm_Celera | 8:88678083 | TGGTGATTTCTAACA[-/G]GGAAGGGACATTTGA | 257632 |
rs220311907 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661600 | CATGGTTGTACACAC[C/T]TGTAAGTAGAGGCAG | 257632 |
rs220351445 | in-del | -/TTT | | | intron-variant | Nod2 | Mm_Celera | 8:88681526 | TTATGCATGTTGGGA[-/TTT]TTTTTTTTTTAAAAA | 257632 |
rs220428015 | in-del | -/GGC | | | intron-variant | Nod2 | Mm_Celera | 8:88668122 | GCAATGTTTAAGAAG[-/GGC]GGCACTATCTGTAGG | 257632 |
rs220430633 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88674336 | TTGGCCTATTGAAGT[C/T]GGCAACCAACTTCAT | 257632 |
rs220493490 | in-del | -/G | | | intron-variant | Nod2 | Mm_Celera | 8:88666535 | TCCATGTCTGGGGTT[-/G]GGGCAAAGGCAGAGA | 257632 |
rs220555918 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88674719 | CCCCCTCGCCAAGGG[A/G]TGGGTCCACACACCT | 257632 |
rs220760876 | snp | C/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645473 | TTCCTGGTCCAGAAT[C/G]GAGGTGAACAGTCTC | 257632 |
rs220874420 | in-del | -/TTTTC | | | intron-variant | Nod2 | Mm_Celera | 8:88680937 | GCTTTTTTTTTTTTT[-/TTTTC]CATCTGTGAGGCTTA | 257632 |
rs220936648 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88678519 | TCTATCTGACCCAGT[G/T]AACTGGGGTTCAAAC | 257632 |
rs221079531 | snp | C/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88647094 | AAGGGCTTACAAATC[C/T]CTGAGAGGGTGCATC | 257632 |
rs221098419 | snp | A/T | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88651575 | AAGCAAGCCAGTAAG[A/T]AACATCCCTCCATGG | 257632 |
rs221115164 | in-del | -/TGCTC | | | intron-variant | Nod2 | Mm_Celera | 8:88670888 | TTAGCTCCCATGCTG[-/TGCTC]TGCTCTGCTCTGCTC | 257632 |
rs221186151 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88647709 | GTAACTGAGAAGGAA[G/T]AGGGTATTGGGACCA | 257632 |
rs221401992 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88667682 | TGCCTCCCCCCATTC[A/G]TACCAGAGTTACAGA | 257632 |
rs221454189 | in-del | -/TTTTTTTTTTT | | | intron-variant | Nod2 | Mm_Celera | 8:88659988 | TGTATTTGTTTGGTC[-/TTTTTTTTTTT]TTTTTTTTTTTTTTT | 257632 |
rs221461902 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88672016 | GCAAGAATTCATGAG[A/G]CTACTGGGGTGGTCT | 257632 |
rs221524358 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88670990 | GCCCGCACCGCCCTC[C/T]GAGTGCCCTCCCCCT | 257632 |
rs221560773 | in-del | -/GTGTGC | | | intron-variant | Nod2 | Mm_Celera | 8:88661842 | TAAGTGCACGTGTGT[-/GTGTGC]GTGTGTGTGTGTGTG | 257632 |
rs221617405 | snp | G/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88649773 | GCCAAGAAACAGACA[G/T]GGGCCTTTGTTGATA | 257632 |
rs221621691 | in-del | -/CACCTT | | | intron-variant | Nod2 | Mm_Celera | 8:88675631 | TGGCTTTGAGTCGTG[-/CACCTT]CGCCTGCAGACCCTG | 257632 |
rs221647930 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88672946 | TCACCTCCTCACCTG[C/G]TAAGTGGGAGATTCA | 257632 |
rs221716538 | in-del | -/GTGCGT | | | intron-variant | Nod2 | GRCm38.p3 | 8:88668514 | TGTGTGTGTGCGCGC[-/GTGCGT]GCTCTCGCGAGTGCA | 257632 |
rs221742275 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661809 | TGTGCCTGTATGCAA[G/T]TGTGCATGCACGTGT | 257632 |
rs221765548 | snp | C/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646968 | TACACTTAGACCTCT[C/T]TCCTCAGCTTGCATG | 257632 |
rs221807948 | snp | C/T | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88688303 | CTTTCTGTGGTTTTT[C/T]AAAATGTCACCTTTG | 257632 |
rs221809947 | snp | A/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88683295 | GGTGGTGTTTGAATT[A/C]AAACTGGGAAGGCTC | 257632 |
rs221931842 | in-del | -/CTCCCT | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646815 | TTCTCTCCTCTCCCT[-/CTCCCT]TTCTCTCTCAAATGA | 257632 |
rs221942703 | in-del | -/A | | | intron-variant | Nod2 | Mm_Celera | 8:88648659 | CAGGGTGTAAATGGA[-/A]GGATGAATTGGAGGG | 257632 |
rs222115376 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88677420 | CTTCAGCAATAGAGT[C/T]GTACTGTCTGCTTCT | 257632 |
rs222144580 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88668316 | GACATGTGTGTCAAA[A/G]TGGATCTTTTTGCTT | 257632 |
rs222183225 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88655974 | AAAAAAATAAGCATA[C/T]TTTTGTCAGGAAACA | 257632 |
rs222352421 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88652352 | TGTCAGGCAAGGAGT[C/T]CCACTCCTTGGGTTC | 257632 |
rs222562456 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88679739 | TGTACAAGTCTACTC[A/G]CCCCTGATAGGGAGC | 257632 |
rs222686319 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88659334 | TGCATACAGGGCTCC[A/G]TAGCCATCAGCTAAA | 257632 |
rs222797872 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88676199 | CCTATCCCCCCTGTA[A/G]ACGCTGCCAGTGTCT | 257632 |
rs222831828 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88651719 | CTTCTTGGTCATGAT[A/G]TTTGTGCAGGAATAG | 257632 |
rs222989269 | in-del | -/GGGGC | | | intron-variant | Nod2 | Mm_Celera | 8:88670262 | CAGGGATTTTGGATG[-/GGGGC]GGGGGGTCTCTATCT | 257632 |
rs223096005 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88651021 | CAGCCTGCGTGTCCG[C/T]AATGTGGTGTTGAGT | 257632 |
rs223176274 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88684415 | GAAAACTAAGCCTTG[C/T]AGTAACTCATCTTGT | 257632 |
rs223292754 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651069 | CCCAGAGCATTCCAG[C/T]CCCAGGCTTCTCTGG | 257632 |
rs223364191 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88676160 | AACGAGCCACCAAGT[A/G]CTCACATGACACCTG | 257632 |
rs223410101 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88649963 | AGGTACAAGAACGAG[A/G]TTCTGGGACTAACTA | 257632 |
rs223410271 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88657541 | ATCTCCCATTTTGAC[A/G]CTTTCTTTGGGCATA | 257632 |
rs223462289 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88657142 | CCTCTCAAGTACTGA[G/T]ATTACAAGCATAATC | 257632 |
rs223557173 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88657240 | ATGCTTTAACACCTG[C/T]AGCATGTAAAAGCTA | 257632 |
rs223558611 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88673682 | TGGCTTCCCAACATA[C/G]TATGGGCATATTTCA | 257632 |
rs223658767 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88657692 | TAGTAGTTTATTTCT[A/G]TAGAATTTTTCTCAT | 257632 |
rs223659636 | in-del | -/G | | | intron-variant | Nod2 | Mm_Celera | 8:88654819 | AAGAAAGAATGAAGT[-/G]GGGGTCAGATGCCTT | 257632 |
rs223744419 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88678599 | CTCTGTGGTCATCCA[A/G]TTCCTGATGTTTATG | 257632 |
rs223790740 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88647830 | CCTTACCCAGAGGGA[A/G]AAAACCCTGCTTTGG | 257632 |
rs223836693 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88679685 | CCTGTTCAGGTGTCA[A/G]TTATGGTGTGTGACA | 257632 |
rs223870205 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88663205 | CAAATGGCTTGCCAA[A/G]CAAATGGTGGGCCTG | 257632 |
rs223883931 | snp | C/T | | | intron-variant, downstream-variant-500B | Nod2 | Mm_Celera | 8:88684667 | TCTGCACACAGTAGG[C/T]TTACATCTCTGGCTG | 257632 |
rs224048899 | snp | A/G | | | downstream-variant-500B | Nod2 | Mm_Celera | 8:88688749 | AGTAGATGTCTTTTA[A/G]CAGGAAGAAGGCAGG | 257632 |
rs224096395 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88662550 | AGGAGAACTAAGCTC[C/T]CATTAGGAAGTGCTT | 257632 |
rs224121811 | in-del | -/TT | | | intron-variant | Nod2 | Mm_Celera | 8:88657339 | TGATATTAATGGCTG[-/TT]TTTTTTTATTTATAT | 257632 |
rs224132098 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88670111 | TATGGGGTGACTGTC[A/G]TGGTCATTATCCGTC | 257632 |
rs224185414 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88686428 | TTGGGCTGGTTGGGA[A/G]CAACCCTGGGTGGCT | 257632 |
rs224442216 | snp | A/C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88669352 | CACACACACACGCGC[A/C/G]CCAATAGGGGCAGGT | 257632 |
rs224521642 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88652189 | TGGCATACCAATGGG[C/T]TCTGAACCAACTTTG | 257632 |
rs224527675 | snp | C/T | | | missense | Nod2 | Mm_Celera | 8:88664648 | CCGGACTCCTCCCCA[C/T]TCGGTCTGGGACCTG | 257632 |
rs224579185 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661544 | CATTAGACAGTTCCC[G/T]GACACAAGATGCTTC | 257632 |
rs224769856 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88665840 | AGAAACAGTGGAGGG[A/G]TTCTGTTTACTGCCT | 257632 |
rs224775954 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88656067 | CTTCCTTGGGAGTCT[A/G]TTAGGGACCTTCTAG | 257632 |
rs224853077 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88656805 | CCATAATATGCTGAA[A/C]TTTGTAATCATCTAC | 257632 |
rs224867562 | in-del | -/TCAGA | | | intron-variant | Nod2 | Mm_Celera | 8:88662752 | GGGGCCGGGGGGGCG[-/TCAGA]TCTGGGAATCAGATC | 257632 |
rs224900523 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88684339 | TACAGAAGCATTGAC[C/T]CTCATGGGTCATCTC | 257632 |
rs224974364 | in-del | -/C | | | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88646569 | GCTCTCTCTCTCTCT[-/C]TCTCTCTCTCTCTCT | 257632 |
rs225018415 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88680221 | AGGAGTCTCCCTGCA[G/T]ATAATGTTTCAATCT | 257632 |
rs225043581 | in-del | -/GAGTA | | | upstream-variant-2KB, utr-variant-5-prime | Nod2 | Mm_Celera | 8:88647336 | TGGGGCGATGGGCGG[-/GAGTA]GATCACTGAGGGAGT | 257632 |
rs225124131 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88681172 | GGTCTCTGCATGGTA[C/T]AAGAGCAAGAGACCA | 257632 |
rs225161075 | in-del | -/TGTGTTTGTGCA | | | intron-variant | Nod2 | Mm_Celera | 8:88661839 | ACGTAAGTGCACGTG[-/TGTGTTTGTGCA]TGTGTGTGTGTGTGT | 257632 |
rs225277909 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88658752 | GGAAGATTAATAAAG[A/G]AGTGGATCTGTCTGT | 257632 |
rs225317987 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88685763 | ACTCACTGTGTAGCC[A/G]AGGATAAACTCCTAA | 257632 |
rs225361765 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88686161 | TTGTTTTGGTTTTTT[A/T]AAAAAATAATTGCAT | 257632 |
rs225373781 | in-del | -/TCCATCCA | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658400 | CCACCCACCCACCTG[-/TCCATCCA]TCCATCCATCCATCC | 257632 |
rs225389629 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658480 | atccatccacctact[C/T]acccacccagccact | 257632 |
rs225401509 | in-del | -/TGTG | | | intron-variant | Nod2 | Mm_Celera | 8:88659730 | CGTGTGTGACCAGCA[-/TGTG]TGTGTGTGTGTTTGT | 257632 |
rs225465809 | in-del | -/GGCAGGGT | | | intron-variant, downstream-variant-500B | Nod2 | Mm_Celera | 8:88684542 | TGGTAAGGGCCCTGG[-/GGCAGGGT]GGGGAACTTCTGTGC | 257632 |
rs225550323 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88672653 | GCTATACCTTCCTTG[A/T]TCTTCTGTGTCTTCC | 257632 |
rs225685661 | in-del | -/GGGAGGGAGGGAGG | | | intron-variant, downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88684844 | TGAAAAACAGAGAGA[-/GGGAGGGAGGGAGG]GAGAGAGAGAGGGAG | 257632 |
rs225793412 | snp | C/T | | | synonymous-codon | Nod2 | Mm_Celera | 8:88660596 | CTGGCTGCCTTCCTT[C/T]TACAGCACGTCAGGG | 257632 |
rs225793656 | in-del | -/CGCGCG | | | intron-variant | Nod2 | Mm_Celera | 8:88669347 | ACACACACACACACA[-/CGCGCG]CCAATAGGGGCAGGT | 257632 |
rs225928742 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88673878 | AAAGCCCTACCTCAG[G/T]CCATATCCAATCTAA | 257632 |
rs225933424 | snp | C/T | | | downstream-variant-500B | Nod2 | Mm_Celera | 8:88688932 | GGCCATCTCCCTGGG[C/T]GTTTGTGTGAGGTAT | 257632 |
rs225940987 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88663661 | AGGTCCCGCTGTGAC[A/C]GTGGCTTCACCCTCA | 257632 |
rs226012088 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88665778 | GAAAAAGTTTATTTT[A/T]TTTCGCAGGGTACAG | 257632 |
rs226068910 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88667177 | CAGTGCTGTGCCTTC[A/T]GCTGGCTGAGCCTAC | 257632 |
rs226099745 | snp | A/G | | | synonymous-codon | Nod2 | Mm_Celera | 8:88664920 | TGCTGACACATCGGT[A/G]GCCTCTCTCAAGCAC | 257632 |
rs226310794 | in-del | -/GAT | | | intron-variant | Nod2 | Mm_Celera | 8:88654285 | CAACTTCCCTGGGCA[-/GAT]GAAATGAGCATCTCT | 257632 |
rs226312673 | snp | C/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645841 | CAGCATCCTTCAGTT[C/T]CTACCTATTTCTGGG | 257632 |
rs226322031 | in-del | -/GT | | | intron-variant | Nod2 | Mm_Celera | 8:88652091 | GAGGGGCTGCATGCA[-/GT]GTGTGCTGCTGAATT | 257632 |
rs226402853 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88671283 | GCCTTTTATGATTTG[C/T]AAAGCAACAGTGAAG | 257632 |
rs226409530 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88686251 | AAGGGCTCTAATGTG[C/T]CTTGCTGACTCTTGA | 257632 |
rs226512796 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88647917 | TGTGTCTTTTTCAGA[A/G]CCTGCAGGGTCCTGG | 257632 |
rs226549353 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88675620 | TCAGCCGATTTTGGC[-/T]TTTGAGTCGTGCGCC | 257632 |
rs226554028 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88662789 | TGCTCTCTGTGGCCA[-/T]TTTTTTTCTTGTGGT | 257632 |
rs226558842 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88673829 | GTTGTTGTTGTCTTA[C/T]CACAATGCCTTATCT | 257632 |
rs226678136 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88658131 | CCATGTGTCCATCCA[C/T]CTGTCTATCCATCTG | 257632 |
rs226704808 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88651931 | CCTGACTAAGACACC[A/G]GGCTCTGCCCCAGGC | 257632 |
rs226810531 | in-del | -/AGAAGCATTGACT | | | intron-variant | Nod2 | GRCm38.p3 | 8:88684327 | AAGGGCTCTCTTTAC[-/AGAAGCATTGACT]CTCATGGGTCATCTC | 257632 |
rs226841847 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88665546 | TTGCCGATTGGGCCT[A/G]TGGCAAATGCTACTG | 257632 |
rs226861308 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88659877 | TGTGGAGAGAGAGAG[C/T]TTAAGCATCCAGGCC | 257632 |
rs226957433 | snp | A/T | | | intron-variant, downstream-variant-500B | Nod2 | Mm_Celera | 8:88684588 | CTTTTAGATCTGTGA[A/T]ATGAGATGAGGGGAG | 257632 |
rs227077889 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88662206 | CTGACTgcagcagca[C/T]ggcctttaatcccag | 257632 |
rs227156328 | snp | G/T | | | synonymous-codon | Nod2 | Mm_Celera | 8:88664383 | CACAGAGTTGCAACT[G/T]AAGGGCTTCTCTGAA | 257632 |
rs227227233 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88666513 | CTTGGAACATCTGTG[A/G]GCCTCTTTCCATGTC | 257632 |
rs227247813 | snp | A/G | | | utr-variant-5-prime | Nod2 | Mm_Celera | 8:88647373 | TAGTGTGGAGTCACC[A/G]CAAAACTGGCGAGGG | 257632 |
rs227376227 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88647982 | TCTCACCCACGGTTG[A/C]TACCCTGCAGGGGAA | 257632 |
rs227488684 | in-del | -/TTC | | | intron-variant | Nod2 | Mm_Celera | 8:88659991 | ATTTGTTTGGTCTTT[-/TTC]TTTTTTTTTTTTTTT | 257632 |
rs227516303 | snp | G/T | | | synonymous-codon | Nod2 | Mm_Celera | 8:88674927 | GGGCAACAGCGTGGG[G/T]GATAAGGGCACCCAA | 257632 |
rs227556360 | snp | C/T | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88686876 | CTTTTCCCGAGGAGT[C/T]GTGATGGTTGGTCTT | 257632 |
rs227569212 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88648062 | ATTGGCTCTGGTCTG[C/T]TCAGTCTGTTGTGAG | 257632 |
rs227587892 | snp | C/T | | | missense | Nod2 | Mm_Celera | 8:88660624 | GGGAACTACCAGCTC[C/T]ACTGCCTCTGCCTTA | 257632 |
rs227632632 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88655510 | TATGAGAGCTTTGTA[C/T]AGTTTTGCTCAGTTG | 257632 |
rs227688005 | snp | C/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646279 | GGACAAGAGGAGTGC[C/G]CTACAGGTGGGGTTA | 257632 |
rs227729848 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88648927 | ACATCATGGCATAGA[G/T]AGAACCTGTGGCTTT | 257632 |
rs227889819 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88676918 | GGTCACTATATATGG[A/C]CACCTATAGCTAAGA | 257632 |
rs227891750 | snp | A/G | | | synonymous-codon | Nod2 | Mm_Celera | 8:88670690 | CAAACTCACGGATGC[A/G]TGCGCCTGCTCCATG | 257632 |
rs227905065 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88678954 | TTGTTGGATTATAGA[-/T]TTTTTTCAATTTTTT | 257632 |
rs227962414 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88679010 | AACTGAAGGTTGGAC[-/T]TAGAGGGTATCTTTT | 257632 |
rs227966970 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88669545 | CAATGCCTCCCTGCT[A/G]GTGTAGACTCTTACC | 257632 |
rs227971516 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88654550 | GTGTCCAGGGAGGGA[G/T]TCTCTAAAGGGTTTG | 257632 |
rs228025612 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88668917 | TGTCTGTGGAGCTCA[C/G]TAATAGGGCAGAAGA | 257632 |
rs228114666 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88686136 | TTGTTTGTATTGCTG[C/T]TGTTTTATTTTGTTT | 257632 |
rs228154103 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88666105 | TTAGGCACTGTGCTA[G/T]ACTTTCTGAAATAAC | 257632 |
rs228348741 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88672773 | GGTAGGTTTGCTTCA[A/G]AGATAGAGGGTGTGC | 257632 |
rs228390717 | snp | G/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650802 | ACTCAGTCCACGATT[G/T]GGCCCCAGCTCATGC | 257632 |
rs228391825 | snp | C/T | | | synonymous-codon | Nod2 | Mm_Celera | 8:88660640 | ACTGCCTCTGCCTTA[C/T]GAGGGTACGTATTTG | 257632 |
rs228642556 | snp | C/T | | | synonymous-codon, downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88684489 | GGTGCAGAAGCCCTC[C/T]TGCAGGCCCTCAGCA | 257632 |
rs228747702 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88672062 | CAGCACAGGTCTTGG[A/G]TTAGCTTCTTGGTAC | 257632 |
rs228819852 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88673389 | ACATTTATGTACCAC[A/C]TAGCTTTTATGGTTT | 257632 |
rs228826090 | snp | A/C | | | missense, downstream-variant-500B | Nod2 | Mm_Celera | 8:88684492 | GCAGAAGCCCTCCTG[A/C]AGGCCCTCAGCAGGA | 257632 |
rs228863057 | snp | G/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645707 | AATACCCACAGACAA[G/T]AAATAAATGTAAACT | 257632 |
rs228898356 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88679275 | GCCAACCGCCTTGAC[C/T]CTTGTATGCTTGCCT | 257632 |
rs228914430 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88677109 | CCTGGACCATCCTGA[C/T]GTACAGCACCAGACA | 257632 |
rs229097252 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88648286 | CTCTGGTTCCACAGC[C/T]ACCCCCGCCCCCACG | 257632 |
rs229101686 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88656401 | AGCTTCCCTCATAGT[C/T]GATTGACAGTTTGAC | 257632 |
rs229131328 | snp | G/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651366 | GGGTGTACTGGCTGG[G/T]TTTGTGTGTCAATTT | 257632 |
rs229218070 | snp | A/G | | | synonymous-codon | Nod2 | Mm_Celera | 8:88675525 | CAAGTCACTAGAGGA[A/G]CTCTGGTGAGTTATG | 257632 |
rs229218709 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88666981 | TGCAGCCCTTAAGTT[A/G]GGAAATAGGGGGAAA | 257632 |
rs229503516 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88658165 | ATCTGTCCATCCACC[C/T]ACCTACCCACCCACC | 257632 |
rs229674511 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88684027 | CAAGGAGTAAAAGTT[C/T]CCATTGTGGATCAGC | 257632 |
rs229702392 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88651906 | AAAAAAAAACACACA[A/C]AAAAAAAAACCTGAC | 257632 |
rs229851597 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88683079 | AGGCCCGGGTTAGAG[A/G]GAGGATTATTATTCG | 257632 |
rs229860646 | snp | C/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88686262 | TGTGCCTTGCTGACT[C/G]TTGATGAAGCTGGGT | 257632 |
rs230005358 | in-del | -/GGG | | | downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88688556 | TTTAAAGTACCACAA[-/GGG]GGGGGGGGGACAATG | 257632 |
rs230005660 | snp | A/G | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88687696 | CTCTGAATGGCCAGG[A/G]TTCTGAAGGGTTCAG | 257632 |
rs230023234 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88651883 | GAGAAACCCTGTCTC[A/G]AAAAACCAAAAAAAA | 257632 |
rs230103655 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88657191 | CTGTTTTCTGTATGG[C/T]ATTTTAAACCCTGAA | 257632 |
rs230144716 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88685622 | CAAGACAAGCATGTT[C/T]TTCAGTATTTTCTCA | 257632 |
rs230262815 | in-del | -/GG | | | intron-variant | Nod2 | Mm_Celera | 8:88670353 | GGTGAGGGTCTCCTT[-/GG]GGGGGGGGTTGTCTC | 257632 |
rs230342742 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88655876 | TTTCTATGCCTTTTG[C/T]AAGAAATTTCCAAAA | 257632 |
rs230354125 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651318 | TTTCTTCCGCTTCCT[C/T]CTTGCCTGTGCTCTT | 257632 |
rs230403946 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88657898 | GTGCCTGGATTCTCC[C/T]AGTCCTGGGATCCTT | 257632 |
rs230435782 | snp | C/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88674705 | CCCTGAGGTGGATTC[C/G]CCCTCGCCAAGGGGT | 257632 |
rs230473447 | in-del | -/A | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646735 | TCATATCTACAATAC[-/A]AATCTTCGGAACCTC | 257632 |
rs230473631 | in-del | -/A | | | intron-variant | Nod2 | Mm_Celera | 8:88671577 | CTTTCATCATGGCTG[-/A]AAGCAGGGACTCTGG | 257632 |
rs230603819 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88685940 | CAGACCCACAAGGCC[C/T]ATTACCTAGACTGGG | 257632 |
rs230720910 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88679656 | CCCCAACTCATCTGT[A/G]GTTCTGTCGTGTCCC | 257632 |
rs230923967 | snp | A/G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88675546 | GTGAGTTATGGGGGG[A/G/T]TTGCCTAGCCTCGTC | 257632 |
rs231013037 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88683392 | CTCGGGACATCACTG[A/G]TTGGGTGTGGATGTG | 257632 |
rs231027666 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662002 | CTTACCCATTAGGCT[A/G]TCGTGCCAGCACTAG | 257632 |
rs231066524 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88680183 | TTCCTGAAGTGATTT[A/T]GAATTGTTTACCTTC | 257632 |
rs231168276 | in-del | -/TGATA | | | intron-variant | Nod2 | Mm_Celera | 8:88649050 | GTCTGCGAGGGGAGC[-/TGATA]TGATAGGAGGGAGAG | 257632 |
rs231180929 | snp | C/T | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88686840 | AGCAGAGAAAGTCAC[C/T]CCATTGCCGTCTGGA | 257632 |
rs231209089 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88671022 | ACCCCGTGTCTATGA[G/T]CTCAAGTTCTTTGTG | 257632 |
rs231305670 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88675006 | TAAGTTGCAAGATGT[A/G]TGCCATGTCATTGTC | 257632 |
rs231383874 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88666062 | GACAACCAAGATTAG[C/G]CATCGCAGCCAGACT | 257632 |
rs231424872 | snp | A/G | | | synonymous-codon | Nod2 | Mm_Celera | 8:88664347 | GGATGCTGTGTCAGC[A/G]CTCCTCAGGAAGTTC | 257632 |
rs231468635 | in-del | -/A | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645387 | GTGTGTGTGGGGGGG[-/A]GGCAGCTGGTAGAAA | 257632 |
rs231568696 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88673141 | GGTTGTTGAGAACTG[A/G]GGATTGTGAGATCCA | 257632 |
rs231696729 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88682219 | TCACAGGGCTTGCCT[A/G]AGACCATCAGAAAGC | 257632 |
rs231698874 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88667115 | GGAGCTTTAGGAAGG[A/G]ATGCATCTGAGGTAA | 257632 |
rs231723810 | in-del | -/CGGAGAT | | | intron-variant | Nod2 | Mm_Celera | 8:88651970 | TTACAAACTGGCCTA[-/CGGAGAT]TTTCTCTGCCGCGTA | 257632 |
rs231846312 | in-del | -/ATCCATCCATCA | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658415 | TCCATCCATCCATCC[-/ATCCATCCATCA]ATCCATCTATCCATC | 257632 |
rs231867941 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88659606 | AGGTGGAGACTACAG[A/G]ATGTGCTGACAATGT | 257632 |
rs231993031 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88687498 | CCCTCTGCCCCCATT[A/G]GGTCTGTTCTTCAGG | 257632 |
rs231994030 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88666115 | TGCTATACTTTCTGA[A/G]ATAACCCCATCCATC | 257632 |
rs232051725 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88673544 | AGCCACCATGCCTGG[C/T]TTCCATTTAACATCT | 257632 |
rs232120213 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88654471 | GACCAGTAGTGGGGA[C/T]AGAACCAGCCCACCC | 257632 |
rs232240565 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88681259 | TGTGTACCCATGACT[G/T]CCGTGTGTCACTTGG | 257632 |
rs232413890 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88663169 | GTTTCTACAGCTAAG[A/G]ACACTGGATCCTGGG | 257632 |
rs232750991 | in-del | -/CCT | | | intron-variant | Nod2 | Mm_Celera | 8:88685709 | ACCCCTACCCCACCA[-/CCT]CAAGATAGAACCTCA | 257632 |
rs232811476 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650707 | TTCTCTTAGTAGGAA[-/G]GGGCACTGGTTACTT | 257632 |
rs232862874 | in-del | -/AT | | | intron-variant | Nod2 | Mm_Celera | 8:88677801 | CACTGTTTTAAGTAC[-/AT]ATGTCACGTATGTAT | 257632 |
rs232877388 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661820 | GCAAGTGTGCATGCA[C/T]GTGTACGTAAGTGCA | 257632 |
rs232892597 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88660871 | GCCAAGGCGTGTGGA[A/G]AGAGCCAGCTATGGG | 257632 |
rs232904053 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88668963 | CCACTTCCCTGAGAG[C/G]CCTAGAAAAGCCCTC | 257632 |
rs232975637 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88674869 | TGAAAGCACATGAAC[A/G]CGTACATGCCTAAAA | 257632 |
rs232986294 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88668239 | TTTACCCCTTTATCA[C/T]GATGTGCTGCCTTGA | 257632 |
rs232996130 | in-del | -/C | | | intron-variant | Nod2 | Mm_Celera | 8:88668963 | CCACTTCCCTGAGAG[-/C]CCTAGAAAAGCCCTC | 257632 |
rs233003972 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88659603 | tgaaggtggagacta[A/C]aggatgtgctgacaa | 257632 |
rs233020931 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88677140 | TGAACTCCCTTTTGC[A/G]GAATGGGCCTAAAAT | 257632 |
rs233046260 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88662537 | CCCATTTCTTGAAAG[A/G]AGAACTAAGCTCTCA | 257632 |
rs233083121 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661309 | AACCTAATATAGACT[C/T]CTGGTCCATGAACTA | 257632 |
rs233099453 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88668655 | CCATGCCAACTGAAA[C/T]CCTGGTCTCTAAGAA | 257632 |
rs233317350 | snp | C/T | | | missense | Nod2 | Mm_Celera | 8:88663721 | TGTCAGAAGTTCATA[C/T]CTAAGCTGAGGACCA | 257632 |
rs233353384 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88675226 | TGGCTGTGAGCTGAA[A/C]CTACCAGATAAGGAC | 257632 |
rs233382840 | snp | A/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88686246 | CACCTAAGGGCTCTA[A/C]TGTGCCTTGCTGACT | 257632 |
rs233409104 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88685161 | GTCTTCAAAGTGAGT[C/T]CCAGGACAGCCGAGG | 257632 |
rs233415034 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651084 | CCCCAGGCTTCTCTG[A/G]CTGGGCTTGGAGTTA | 257632 |
rs233516424 | in-del | -/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88678684 | CTTGGGGACGGACTT[-/C]CCTCATAATGTCTTG | 257632 |
rs233555911 | snp | G/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646060 | AACCTGCTCTAGAGC[G/T]GCTCCCAAATAAACC | 257632 |
rs233609191 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88651504 | CGTGTGGGTGGGACC[A/G]TCTCTGGGCTGGTTG | 257632 |
rs233629613 | in-del | -/ACAT | | | intron-variant | Nod2 | Mm_Celera | 8:88683654 | ACAGGATGGACACAC[-/ACAT]ACACACACACAGAGA | 257632 |
rs233679525 | in-del | -/A | | | intron-variant | Nod2 | Mm_Celera | 8:88674535 | GGGGGATTAAGAAGG[-/A]AAAAAAGAGATGAAA | 257632 |
rs233774445 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88669809 | GACGTCACTGGGTAC[C/T]TATCCCCAGGCTACC | 257632 |
rs233827518 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88675720 | TTGCCTGCACATGCC[A/G]TAATGGTGAAGACCA | 257632 |
rs233828169 | snp | A/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646688 | TTTTCCCTGCTCTGG[A/G]CTCTTCCAGATGCCT | 257632 |
rs233848851 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88669408 | CAGTGATGTTTCAGG[A/G]GGTTTAGGAGGTACG | 257632 |
rs233874733 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88672461 | ACACTGAGGATGGCT[A/G]AGACCAAGAACGAAA | 257632 |
rs233959784 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88674452 | CAGAACGTGAGGACT[A/C]TTTCCAACCTATTGT | 257632 |
rs234034340 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88686586 | GCAAGCCTTCACTCA[A/C]ACCTCCCTCTCCACT | 257632 |
rs234036024 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88652856 | CTGACCTCCCCTGCT[C/T]TCTTACAGGTTGTGA | 257632 |
rs234081645 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88681451 | ACAGTGGAAGCATGG[A/G]CCACCTTTGCACGGC | 257632 |
rs234099517 | snp | C/G | | | missense | Nod2 | Mm_Celera | 8:88664082 | TGGCCAAACCGCTGT[C/G]CCTGAGGACGCTGCT | 257632 |
rs234144187 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88659779 | CACATACTTATGACA[C/T]ATTTAAAAGGAAAAA | 257632 |
rs234208594 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88659230 | GGGATGGAATAGGCT[A/G]TAGGCAAGGATTGTG | 257632 |
rs234293217 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88675894 | GAGCCTGCCATGTGT[A/G]TATGTGCTTAGTATA | 257632 |
rs234332223 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658423 | ATCCATCCATCCATC[C/T]ATCCATCTGTCCATT | 257632 |
rs234336779 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88673691 | AACATAGTATGGGCA[C/T]ATTTCAGACCAGTAT | 257632 |
rs234364926 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88680240 | ATGTTTCAATCTCAG[A/G]GGGAACTGTTTCATA | 257632 |
rs234428233 | in-del | -/GGC | | | intron-variant | Nod2 | Mm_Celera | 8:88670264 | GGGATTTTGGATGGG[-/GGC]GGGGGGTCTCTATCT | 257632 |
rs234496152 | in-del | -/CAGAATGGACACACACACACACACACACACACACACACACACACAGAGAGAGAGAGAGA | | | intron-variant | Nod2 | Mm_Celera | 8:88683682 | AGAGAGAGAGAGAGG[lengthTooLong]GAGAGAGAGAGAGAG | 257632 |
rs234531261 | snp | A/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646904 | GCGAATTCCGATTAG[A/G]ATGGTGGCAGAGCCC | 257632 |
rs234653552 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88682443 | GTTGGAGCACGGATG[A/G]GAAGGCTGATAAGTG | 257632 |
rs234817106 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88647717 | GAAGGAATAGGGTAT[A/T]GGGACCAAATTGAAG | 257632 |
rs234896759 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88663086 | GAGGCAGTACTATTA[A/G]CTGGGGACCAAGCAT | 257632 |
rs234958061 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88648332 | ACATCCTCAGCCCAT[A/G]CAGACCCCATCTGTA | 257632 |
rs234979339 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88654416 | GTGTACCTTCCATTA[A/G]CATTCAAAAGCACAT | 257632 |
rs235223956 | in-del | -/C | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645531 | GGTTTCCACCATGCT[-/C]CCCCAACCCCTCCTC | 257632 |
rs235285186 | in-del | -/GCACC | | | intron-variant | Nod2 | Mm_Celera | 8:88675636 | TTGAGTCGTGCGCCT[-/GCACC]GCAGACCCTGGTGCT | 257632 |
rs235300564 | snp | C/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650208 | CTGCCTCGCCCTGCC[C/G]GTGTCCACACTGCTG | 257632 |
rs235318449 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88671901 | AGCAGAAAATGCCCA[C/T]GGGTAGTGGGAGAAT | 257632 |
rs235357687 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88677407 | GCACACGTGGTGTCT[C/T]CAGCAATAGAGTCGT | 257632 |
rs235404046 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88656745 | CTGAGACTTCAAAGA[C/G]CATTTGCTATCTCTT | 257632 |
rs235513437 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88649606 | CTAGGACAGCTCAGG[C/G]CTGCATTCTGCTCTC | 257632 |
rs235557528 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661083 | TACCAGGCAGCCTGG[C/T]ATACACTCTATGGAA | 257632 |
rs235571961 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88654191 | AGGTGTTTGGTGAGT[A/G]CTTGTTGGTGAAATA | 257632 |
rs235614992 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88668594 | GAAGAAGGGGTCAGC[A/T]TTTCTCCCACAGTAT | 257632 |
rs235624678 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661494 | CTTGGGGAGTATTTA[C/T]TGACAATGTCATCAA | 257632 |
rs235682145 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661644 | TCAAGGTCATCTTCC[A/T]TTACAATATCAAGTT | 257632 |
rs235827227 | in-del | -/AGAG | | | intron-variant | Nod2 | Mm_Celera | 8:88655914 | TAATGAAAGAAAGAA[-/AGAG]AGAGAGAAAGAAAAG | 257632 |
rs235892211 | in-del | -/A | | | intron-variant | Nod2 | Mm_Celera | 8:88655957 | AAGAAAGCAACTAAG[-/A]AAAAAAAATAAGCAT | 257632 |
rs235917929 | snp | C/T | | | intron-variant, downstream-variant-500B | Nod2 | Mm_Celera | 8:88684711 | TATCTCCCAGTAGGG[C/T]CAGTTCTGCTTCAAA | 257632 |
rs235967239 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88684420 | CTAAGCCTTGTAGTA[A/G]CTCATCTTGTCTACG | 257632 |
rs235972506 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88656855 | AGAGGCCATTTGAAT[C/T]CAGAAACTTGCGTCT | 257632 |
rs236067541 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88676488 | GCTTACTTACAGGAA[C/G]AGAAATGACTCAAAG | 257632 |
rs236094528 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88685063 | TCAAAGTAAAGAATA[C/G]TGGTTTAGTTGCCGG | 257632 |
rs236184947 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88682688 | GTGGCTAGGACAGAG[C/T]GGGCTCACATTCTCC | 257632 |
rs236221980 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88647505 | GAGACCGAGGACTCC[C/T]GGGCAACAGCGCTTG | 257632 |
rs236324263 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88649487 | AATGAAGGATGAATT[A/G]ATCTGTTTGTTCTCT | 257632 |
rs236350693 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88679450 | CCTAATTGTGAGGGC[A/G]CAGCCTTAGTTGCTC | 257632 |
rs236364356 | in-del | -/A | | | intron-variant | Nod2 | Mm_Celera | 8:88679035 | TCTTTTTTTTTTTTT[-/A]AATCACTTTTACTGT | 257632 |
rs236393688 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88684121 | GTCAGTGAGGTGCTG[A/G]GCCAAGAGCTCTTGC | 257632 |
rs236552550 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88686162 | TGTTTTGGTTTTTTA[A/T]AAAAATAATTGCATA | 257632 |
rs236629024 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88670778 | CTTCTTTTCTGAATC[C/T]GACATTCCCAGAGCT | 257632 |
rs236649085 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88652081 | GATTGTGGCAGAGGG[A/G]CTGCATGCAGTGTGT | 257632 |
rs236706314 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88663446 | ACTAGGTGGCATGCA[-/T]CACCATCCTTGTTTA | 257632 |
rs236712605 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88659760 | TTGTGTGTGCATGCA[C/T]GCGCACATACTTATG | 257632 |
rs236724174 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88657705 | CTGTAGAATTTTTCT[C/T]ATGGGTTTACCAGCT | 257632 |
rs236785847 | snp | G/T | | | missense | Nod2 | Mm_Celera | 8:88664826 | GTGCCCAAAGTAGTG[G/T]GCCCGGGAGCAAGGC | 257632 |
rs236826299 | snp | C/T | | | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88646557 | tgctctctcttggct[C/T]tctctctctctctct | 257632 |
rs236840559 | in-del | -/ATCC | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658444 | CTGTCCATTCCATCT[-/ATCC]ATCCATCCATCCATC | 257632 |
rs236910380 | in-del | -/TCCTT | | | intron-variant | Nod2 | GRCm38.p3 | 8:88678574 | CTAGTAATATTTGCT[-/TCCTT]CCTCCTCTGTGGTCA | 257632 |
rs236928496 | in-del | -/AAGGA | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650557 | TGTGCTTTGCAGAAG[-/AAGGA]AAGGAAACAGTAAGT | 257632 |
rs237069454 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88678124 | CACATAGCTATTTAG[C/T]TTGTCTTACAAGGAT | 257632 |
rs237225032 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88648524 | TCTTAAGGAGGGGAT[A/T]GGCAAGTCATGTGAC | 257632 |
rs237230633 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88667383 | CTAGTGGGCCAAGCC[-/T]TTTTTTTTTCAAGAC | 257632 |
rs237238890 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88681371 | TGTTGAGCTAGGAAA[A/G]AATGAGACATTCATA | 257632 |
rs237278556 | in-del | -/ACGG | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650257 | GGATGGTTTGGGTAT[-/ACGG]CAGGCAGGCTCTTAA | 257632 |
rs237293514 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88648828 | TGACTTAAGGTTTGG[C/T]AGGGTTCATCAAGTT | 257632 |
rs237517285 | in-del | -/TGGGGAGTC | | | intron-variant | Nod2 | Mm_Celera | 8:88686345 | AGCAATAGCTGGCCT[-/TGGGGAGTC]TGTAGCTGGCCTGGC | 257632 |
rs237554885 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88665895 | gctttttagtacaca[A/C]caggcccacctgtct | 257632 |
rs237615176 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88672442 | GAGGGTTATGCTGGC[A/G]TGTACACTGAGGATG | 257632 |
rs237694355 | in-del | -/GGT | | | intron-variant | Nod2 | Mm_Celera | 8:88662750 | GGGGGGCCGGGGGGG[-/GGT]CGTCTGGGAATCAGA | 257632 |
rs237704534 | snp | A/C/G | | | synonymous-codon | Nod2 | GRCm38.p3 | 8:88664488 | AGCCACCTCAGCCCT[A/C/G]CATGGTTTGTGCCAC | 257632 |
rs237752272 | snp | A/G | | | synonymous-codon | Nod2 | Mm_Celera | 8:88664572 | GAACAGGGGCTTCCC[A/G]ACAACCAGCACGGAC | 257632 |
rs237773081 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88656953 | TCTATGGAATTGCAG[A/C]TGCTTGAATGCTGGA | 257632 |
rs237855319 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88685455 | AGGCTCCTTGGTCCT[C/T]GTGCAGAAAGCAGAG | 257632 |
rs237863545 | in-del | -/TT | | | intron-variant | Nod2 | Mm_Celera | 8:88661712 | AATTGGGTTTATTTA[-/TT]TTTTTTTAATGAAAA | 257632 |
rs237873841 | in-del | -/TGTG | | | intron-variant | Nod2 | Mm_Celera | 8:88652142 | CTTCCGTCAAGGGTA[-/TGTG]TGTGTATGTGTGTGT | 257632 |
rs237896574 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88663055 | GATTCTGTATCCTAA[A/C]GGTGCTACCTCTACT | 257632 |
rs237898224 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88667759 | TGGTCCTTTTTTTTT[A/G]ATGATTAAGAACGTT | 257632 |
rs237921820 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651020 | CCAGCCTGCGTGTCC[A/G]CAATGTGGTGTTGAG | 257632 |
rs237947195 | snp | A/G | | | intron-variant, downstream-variant-500B | Nod2 | Mm_Celera | 8:88684845 | GAAAAACAGAGAGAG[A/G]GAGGGAGGGAGGGAG | 257632 |
rs238002842 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88677235 | TTGCCTAGCATGTTG[A/G]CATTTCAGCAGGCAG | 257632 |
rs238028740 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88663482 | ATCAAAGTTCCCGGC[C/T]ATATTCCTGCTTTGC | 257632 |
rs238043518 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88668121 | TGCAATGTTTAAGAA[A/G]GGCGGCACTATCTGT | 257632 |
rs238078036 | snp | A/G | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88686988 | TTAGTGACTGGAAGG[A/G]GAAAGGCCCTCACTG | 257632 |
rs238120940 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88678819 | CGCACAAGCCAGGCT[C/T]AGACAGGCTCTTGCA | 257632 |
rs238165387 | snp | C/T | | | synonymous-codon | Nod2 | Mm_Celera | 8:88686684 | ACTGAGCTCCAGGGA[C/T]GCCAGACTCTTGTTG | 257632 |
rs238180130 | in-del | -/TA | | | intron-variant | Nod2 | Mm_Celera | 8:88661862 | GTGTGTGTGTGTGTG[-/TA]GATGCATGTGAGTGT | 257632 |
rs238192546 | snp | A/G | | | downstream-variant-500B | Nod2 | Mm_Celera | 8:88688587 | TGTTGTTTTATACCG[A/G]ATAATATATTGCCTA | 257632 |
rs238317397 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88682606 | GTTCAGACATTGATT[A/G]GAAAAATATTGGCAC | 257632 |
rs238366877 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88686218 | TTCAAGGAGTAGAGC[A/G]GCCTCAGGCTGACAC | 257632 |
rs238415674 | snp | C/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650365 | ACCACCAGGGTCTTT[C/G]AGTGAAAGCCAGTGT | 257632 |
rs238518511 | in-del | -/TGTGCCT | | | intron-variant | Nod2 | Mm_Celera | 8:88659284 | CTGGGTAAGCCATGA[-/TGTGCCT]TGTGCCTTGGAGCAA | 257632 |
rs238582861 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88660806 | GAAAAGATGAGGGCA[C/T]GGCGGCTCTCCCCCT | 257632 |
rs238744012 | in-del | -/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645304 | TTATTGGCAATAGGC[-/T]TTTTTTATTGATAGG | 257632 |
rs238759804 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651557 | GGCTGAGCAAGCCAG[A/G]TGAAGCAAGCCAGTA | 257632 |
rs238776797 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88654964 | ACAGCAAAAGCCAAC[A/C]CTGAAGATGAAGGAG | 257632 |
rs238845900 | in-del | -/CTCCCC | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646809 | CAATTATTCTCTCCT[-/CTCCCC]CTCCCTTTCTCTCTC | 257632 |
rs238846516 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88683682 | CAGAGAGAGAGAGAG[A/G]GAGAGAGAGAGAGAG | 257632 |
rs239051161 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88662163 | AGCCACAAGGATCCT[C/T]GCCTTTGGGAACAAG | 257632 |
rs239148420 | snp | A/C | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645991 | TCTGCCTCCACCCCC[A/C]TCCCCTCCTTGTCTG | 257632 |
rs239200052 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88653349 | AAGCTGTGGCCTGTG[A/T]CAGCAGAATCCACAG | 257632 |
rs239259522 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88674205 | ATGCTGTCATATTAC[A/G]ACTCCATGAAGGGAT | 257632 |
rs239278359 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651311 | GGAAGTCTTTCTTCC[A/G]CTTCCTCCTTGCCTG | 257632 |
rs239312331 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88680463 | CAACAGAACAAGGTG[G/T]TTTTAAAATTATTAT | 257632 |
rs239345456 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662385 | AGAGCTCTCTGACAA[A/G]AACTAGCTTGCCTCT | 257632 |
rs239350261 | in-del | -/C | | | intron-variant | Nod2 | Mm_Celera | 8:88672283 | TTGCTAATTGCTGTG[-/C]CCCTGTGACCCTGCC | 257632 |
rs239387898 | in-del | -/GCTT | | | intron-variant | Nod2 | Mm_Celera | 8:88648212 | GCCCAGTGAGCAGAC[-/GCTT]ACTGCTAACAAAGTG | 257632 |
rs239505790 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88673124 | CTTCCAAGGGAGGGG[C/T]TGGTTGTTGAGAACT | 257632 |
rs239601225 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88658001 | GGAGTGGGGAAGACA[G/T]ACTTGATACTGCCAT | 257632 |
rs239663587 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88674811 | GTGTGGTAGGTCCAC[A/G]TTGCTGGGACCCCTG | 257632 |
rs239719508 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88674354 | CAACCAACTTCATTA[A/C]CTATTTCAGAGTGCG | 257632 |
rs239743439 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88675122 | TGAAAGACCTATGCG[C/T]TTGGGATCAGGAAAC | 257632 |
rs239796506 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88668515 | GTGTGTGTGCGCGCG[C/T]GCGTGCTCTCGCGAG | 257632 |
rs239804545 | in-del | -/GT | | | intron-variant | Nod2 | GRCm38.p3 | 8:88668517 | TGTGTGCGCGCGTGC[-/GT]GTGCTCTCGCGAGTG | 257632 |
rs239823156 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88660080 | TTGGCTGTGTGTTTG[C/T]TTCACAAACCACGAC | 257632 |
rs239865480 | snp | C/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645582 | TGACGCTAAGCCTGA[C/T]AAGCTAAATTCGATC | 257632 |
rs239997417 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88667400 | TTTTTTTTCAAGACA[C/G]AGTTTCTCTGTATAG | 257632 |
rs240090339 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88659360 | CTAAATGTACCAACT[C/G]TAGAAGACATAACAG | 257632 |
rs240092012 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88667615 | TCTCTGGATTTTTAT[G/T]TTTAAGTGGGGCTTC | 257632 |
rs240096235 | in-del | -/CACAC | | | intron-variant | Nod2 | Mm_Celera | 8:88651900 | AAAACCAAAAAAAAA[-/CACAC]ACAAAAAAAAACCTG | 257632 |
rs240171758 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88659887 | GAGAGTTTAAGCATC[C/T]AGGCCATGGGACTTG | 257632 |
rs240225166 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650678 | GCAAGAGTGCTAACA[C/T]CACCTCTGTGCTTTT | 257632 |
rs240226914 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88647592 | TCTGGAGCTGGCCTG[G/T]CTGAGCTCCTGAAAG | 257632 |
rs240254970 | snp | A/G | | | utr-variant-3-prime | Nod2 | GRCm38.p3 | 8:88686965 | CTAAAGAGGATCACC[A/G]TGCAGAATTAGTGAC | 257632 |
rs240288344 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88678623 | GTTTATGGGGACTTC[A/G]GACGCTGATAACAAA | 257632 |
rs240348231 | snp | C/T | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88688278 | CCAAGCCCTTCTTTC[C/T]GAGCAAGGTCTTTCT | 257632 |
rs240490536 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88649979 | TTCTGGGACTAACTA[A/G]TAAAGAACTTCTTCA | 257632 |
rs240536270 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88679826 | TTACTTGTAGGAATG[C/T]GGGTGAGGGGTTACT | 257632 |
rs240582374 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88681722 | CTGTGATGGTACAAT[A/G]ATGCCCAGTGTGGGG | 257632 |
rs240600670 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88677982 | CATAGCTTTTGCTTC[-/T]TTTTTTATGGCCAGC | 257632 |
rs240614331 | in-del | -/A | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88688258 | AGGCTTGCAGGGGAC[-/A]AAAACCAAGCCCTTC | 257632 |
rs240678245 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88683929 | GACACCTATTGGTGG[C/T]GTTCTCATCCTGGCC | 257632 |
rs240681380 | snp | A/T | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88651593 | CATCCCTCCATGGCC[A/T]CTGCATCAGCGCCTG | 257632 |
rs240741662 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651263 | GCCCCCACCCCTTCT[C/T]CTCAGCATCTTAGAA | 257632 |
rs240774088 | snp | G/T | | | downstream-variant-500B | Nod2 | Mm_Celera | 8:88688709 | TCCTTAGTTCCTTAG[G/T]TCTCTCCTGGTGGCT | 257632 |
rs240787546 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88679108 | GGCCAACATGGAGGA[C/T]GCCAGTCACATCTCC | 257632 |
rs240809203 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88672634 | AGAGGCCAGGTGCCA[A/G]CATGCTATACCTTCC | 257632 |
rs240856248 | snp | C/T | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88687288 | TTGGACTACTCTATC[C/T]GGATGGTGTAAGTGA | 257632 |
rs240895849 | in-del | -/CA | | | intron-variant | Nod2 | Mm_Celera | 8:88661849 | ACGTGTGTGTGTGTG[-/CA]TGTGTGTGTGTGTAG | 257632 |
rs241100717 | in-del | -/TA | | | intron-variant | Nod2 | Mm_Celera | 8:88681536 | TGGGATTTTTTTTTT[-/TA]AAAAAGAGGAGGTCA | 257632 |
rs241128722 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88674854 | GGCGGAGTGGCGTTA[C/T]GAAAGCACATGAACA | 257632 |
rs241191687 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88681986 | TGCAACTGGAGCCTT[C/T]GGGAGTTGACAGAAC | 257632 |
rs241205590 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88662702 | AGCCTTTCAGTCTGA[A/C]TAATCCATTTAGCAT | 257632 |
rs241212472 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88654463 | CCTCCTGTGACCAGT[A/C]GTGGGGATAGAACCA | 257632 |
rs241330837 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88687329 | ttccctttctcctcc[C/T]tccctccctccctcc | 257632 |
rs241335569 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88655225 | TTTATAGAGGTGGCT[C/T]TCATTGCTGAAAACA | 257632 |
rs241378809 | snp | C/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88647125 | GGCTCCTACTGACAC[C/T]GAGGGCTTTCCTAGC | 257632 |
rs241393319 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88670124 | TCGTGGTCATTATCC[A/G]TCTGCAAAGATGGGA | 257632 |
rs241401711 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661568 | ATGCTTCTAAAGATG[C/T]CAATTAAGCAGGTGG | 257632 |
rs241462754 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88676161 | ACGAGCCACCAAGTG[C/T]TCACATGACACCTGA | 257632 |
rs241510276 | snp | C/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88647207 | CAGAACACAAAGCAC[C/T]GCAGGCAGGCCTGTT | 257632 |
rs241533921 | snp | G/T | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88651228 | AGGAAAGACCTGGGC[G/T]CCCCAGGCCATTTCC | 257632 |
rs241546469 | in-del | -/ACAGTGAAG | | | intron-variant | Nod2 | Mm_Celera | 8:88671290 | ATGATTTGCAAAGCA[-/ACAGTGAAG]ACAGTGAAGAGTAGC | 257632 |
rs241613174 | snp | C/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646286 | AGGAGTGCCCTACAG[C/G]TGGGGTTAAGAGACT | 257632 |
rs241685850 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88661933 | GAGTTGGCTGTCTCT[C/T]CCATCGTAGTTTTGG | 257632 |
rs241748355 | snp | G/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645381 | AAGCGTGTGTGTGTG[G/T]GGGGGAGGCAGCTGG | 257632 |
rs241764490 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88677421 | TTCAGCAATAGAGTC[A/G]TACTGTCTGCTTCTG | 257632 |
rs241782421 | in-del | -/CACGGAG | | | intron-variant | Nod2 | Mm_Celera | 8:88651968 | AGTTACAAACTGGCC[-/CACGGAG]TATTTCTCTGCCGCG | 257632 |
rs241791434 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88648664 | GTGTAAATGGAGGGA[C/T]GAATTGGAGGGCTGG | 257632 |
rs241797208 | in-del | -/TT | | | intron-variant | Nod2 | Mm_Celera | 8:88655077 | AGAATCTCCCTTGTC[-/TT]TTTGTTCCCTTCAGC | 257632 |
rs241840838 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88647919 | TGTCTTTTTCAGAAC[C/T]TGCAGGGTCCTGGCC | 257632 |
rs241843206 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88648932 | ATGGCATAGAGAGAA[C/T]CTGTGGCTTTCAGAT | 257632 |
rs241934304 | snp | C/G | | | intron-variant, downstream-variant-500B | Nod2 | Mm_Celera | 8:88684562 | AACTTCTGTGCCTCT[C/G]CAAGCCTTGGCTTTT | 257632 |