SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs241980958 | in-del | -/GGCAGTAG | | | intron-variant | Nod2 | Mm_Celera | 8:88649209 | CAGTGATTTGTACTT[-/GGCAGTAG]GGGGGTGGGGTGGGG | 257632 |
rs242023857 | snp | A/G | | | missense | Nod2 | Mm_Celera | 8:88660605 | TTCCTTCTACAGCAC[A/G]TCAGGGAACTACCAG | 257632 |
rs242221941 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88660265 | GTTTTAGAATATTTA[C/T]ATAAACAATGAATAC | 257632 |
rs242269849 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88659761 | TGTGTGTGCATGCAC[A/G]CGCACATACTTATGA | 257632 |
rs242287887 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88673182 | AGAGAGGGTAACTAT[A/G]GGGCCCAGATGTTTT | 257632 |
rs242328134 | snp | C/T | | | missense | Nod2 | Mm_Celera | 8:88664919 | GTGCTGACACATCGG[C/T]GGCCTCTCTCAAGCA | 257632 |
rs242328894 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88667191 | CAGCTGGCTGAGCCT[A/G]CCTGAGGTCACCTTA | 257632 |
rs242355161 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88660957 | CTCAATCCACGAAAC[C/G]TAGTTTCTCATGATC | 257632 |
rs242359776 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88668337 | CTTTTTGCTTTTTAA[A/G]TTAATCACCTCAGGG | 257632 |
rs242437278 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88674710 | AGGTGGATTCCCCCT[C/T]GCCAAGGGGTGGGTC | 257632 |
rs242530697 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88677923 | TTCATTCACAGAGGT[A/G]GAACTGTTAGAGATT | 257632 |
rs242531690 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662217 | AGCACGGCCTTTAAT[C/T]CCAGCGCACACTGGG | 257632 |
rs242599904 | in-del | -/TATATGCACGTG/TGCACGTG | | | intron-variant | Nod2 | Mm_Celera | 8:88669340 | ACACACACACACACA[-/TATATGCACGTG/TGCACGTG]CACACACGCGCGCCA | 257632 |
rs242631866 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88683610 | ATTATTTATATCTCT[C/T]TTCCATGTGAGGTGT | 257632 |
rs242646283 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88674871 | AAAGCACATGAACAC[A/G]TACATGCCTAAAACA | 257632 |
rs242710945 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88682372 | ACAAGGGTTGAGAAC[C/T]GCTGCTCCAGAGAGT | 257632 |
rs242736169 | snp | C/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88656721 | TATCTTCCCTGTTTA[C/G]GGGTTGCACTGAGAC | 257632 |
rs242774534 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88671684 | AGTTGTTTTCGTTCC[A/C]GTCTCTTTCCTTAAA | 257632 |
rs242785619 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88655480 | GGAGTATACACTTCC[C/T]TTTGTGTCATAAGAT | 257632 |
rs243091103 | snp | A/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658292 | attcatccatccacc[A/C]atctatctaccatcc | 257632 |
rs243161719 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88657279 | GTTTCTTTATTACAG[C/T]AACTTGATCTTGTTT | 257632 |
rs243210119 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88686062 | AGTCTGCTTCCTGTG[C/T]GACTGCAGTCCCATT | 257632 |
rs243307324 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88686128 | CTTTTGTCTTGTTTG[G/T]ATTGCTGCTGTTTTA | 257632 |
rs243359446 | in-del | -/CTTGGCACTGGC | | | intron-variant | Nod2 | Mm_Celera | 8:88655314 | CAGGGAAAGTGTGCA[-/CTTGGCACTGGC]CTAGTGTTCTCTCTA | 257632 |
rs243360449 | in-del | -/G | | | intron-variant | Nod2 | Mm_Celera | 8:88685834 | TGCACCGCCATGCCT[-/G]GCTTGGAGCCCCGTT | 257632 |
rs243404237 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88656712 | TTACTCCATTATCTT[C/T]CCTGTTTACGGGTTG | 257632 |
rs243406545 | snp | A/T | | | missense | Nod2 | Mm_Celera | 8:88663837 | GGAGCTGCAGACTGA[A/T]GTGGGCACAGCCGGG | 257632 |
rs243420771 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88663335 | AGGAATAGACAATCA[A/G]GATACAGATCCTGCA | 257632 |
rs243460234 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88663264 | AAGCCCTGCCCCCTT[A/C]TATTTTCCATCAGAA | 257632 |
rs243539870 | snp | C/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88649800 | GATACCCTTGACCCT[C/G]TGTTTCAGAAAGGAA | 257632 |
rs243552814 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88647441 | TGGTTCTGTGGTCTG[C/T]GGGTGATCGGGGTGG | 257632 |
rs243621263 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88675277 | TGGCTGGCCAGTTGG[A/G]GAGGGTTTGGAGGCT | 257632 |
rs243647077 | in-del | -/G | | | intron-variant | Nod2 | Mm_Celera | 8:88651985 | TTTCTCTGCCGCGTA[-/G]GGATCTTAGTGCCTA | 257632 |
rs243651594 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88676922 | ACTATATATGGCCAC[C/T]TATAGCTAAGAAACA | 257632 |
rs243668435 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88662004 | TACCCATTAGGCTAT[C/T]GTGCCAGCACTAGGT | 257632 |
rs243729546 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88663423 | TCCTTTGTGTTGGAT[A/G]CTATACTGACTAGGT | 257632 |
rs243847899 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88679744 | AAGTCTACTCGCCCC[A/T]GATAGGGAGCCCACA | 257632 |
rs243876778 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88681080 | TCCTGTCCCATCATG[C/T]TTAGTGTATGTCTTC | 257632 |
rs243922779 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88663184 | AACACTGGATCCTGG[A/G]AAGGCCAAATGGCTT | 257632 |
rs243933731 | in-del | -/GGG | | | intron-variant | Nod2 | Mm_Celera | 8:88672421 | AAGGGGGTAGGGATT[-/GGG]GGGGGGAGGGTTATG | 257632 |
rs243938969 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88658017 | ACTTGATACTGCCAT[A/G]CCAGAGCTCTTGGCA | 257632 |
rs243960699 | snp | A/G | | | intron-variant, downstream-variant-500B | Nod2 | Mm_Celera | 8:88684679 | AGGCTTACATCTCTG[A/G]CTGTGAAGGAAATCT | 257632 |
rs244039621 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88686276 | TCTTGATGAAGCTGG[G/T]TGGGCACAGACTTAA | 257632 |
rs244113943 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88655584 | GTGATGCCAGCTGTC[C/T]CTGTGACTCATGCAG | 257632 |
rs244161603 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88662731 | ATGTAAGATAACACA[G/T]ACATGGGGGGCCGGG | 257632 |
rs244175970 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88654557 | GGGAGGGAGTCTCTA[A/G]AGGGTTTGAGGAAGG | 257632 |
rs244176072 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88662625 | AGGGGCAAGAAGGAA[A/G]TATCGGAAGGTTTTG | 257632 |
rs244181828 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88652380 | TTCAAACCCTAGCCC[C/T]ATCTTTCCCAGCTAT | 257632 |
rs244231725 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88676690 | GTGAGAGGGACTCCC[A/G]GCTTTTGTTGTTTAC | 257632 |
rs244327217 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88655099 | CCCTTCAGCTCTGGA[C/G]TCTTGGGATCTCTGG | 257632 |
rs244406917 | in-del | -/GA | | | intron-variant, downstream-variant-500B | Nod2 | Mm_Celera | 8:88684872 | GAGAGAGAGAGGGAG[-/GA]AGAGAGAGAGAGAGA | 257632 |
rs244486491 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88673738 | GAGTTGTATAGCCTT[C/G]CCCTGATTGGGTGGC | 257632 |
rs244501238 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88647845 | GAAAACCCTGCTTTG[A/G]GTCTTAGCAGGAACT | 257632 |
rs244602315 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88662749 | ATGGGGGGCCGGGGG[C/G]GCGTCTGGGAATCAG | 257632 |
rs244617827 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88678734 | TAAGGAGGGATGGGA[A/G]ATTAAATTGCTCAGC | 257632 |
rs244957091 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88670950 | AGTTTTTGGTTCCTG[A/G]GGTGGAGAGTTTCTA | 257632 |
rs245026022 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88686254 | GGCTCTAATGTGCCT[C/T]GCTGACTCTTGATGA | 257632 |
rs245199232 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88652042 | GAGTCCCCAGCACTC[A/G]GGTCTGAAGGCTGAG | 257632 |
rs245277175 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88659255 | ATTGTGCAGAGACTG[G/T]CAGCTGTGCAGTTTC | 257632 |
rs245367281 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88666764 | TCCTGTCCGTATTAG[A/G]TGACTTATCTGCTCT | 257632 |
rs245386364 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88678776 | CACAGAAGACTGATG[A/G]ATCCTGTTCATTCCC | 257632 |
rs245442070 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88672172 | AGATGAATTTGATTT[A/G]TATTTATTCTGGAAA | 257632 |
rs245558093 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88656149 | AATCTGGAGCATCTG[A/G]CAGAGCTGGTGTGAG | 257632 |
rs245602282 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650323 | TTGTTTCTGTCTGGG[A/C]AAGCACGTTTATTGG | 257632 |
rs245659578 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88649662 | GTCTGCTGGAGGCCT[-/G]GGGGCACTGCAAAGG | 257632 |
rs245990544 | in-del | -/A | | | intron-variant | Nod2 | Mm_Celera | 8:88651904 | CAAAAAAAAACACAC[-/A]ACAAAAAAAAACCTG | 257632 |
rs245992125 | in-del | -/C | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645696 | TCCACATACATAATA[-/C]CCACAGACAATAAAT | 257632 |
rs245995538 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88665782 | AAGTTTATTTTATTT[C/T]GCAGGGTACAGTCCA | 257632 |
rs246002120 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88673416 | GTTTTTCGAGACAGA[A/G]TTTCTCTGTGTAGTC | 257632 |
rs246251578 | in-del | -/C | | | intron-variant | Nod2 | Mm_Celera | 8:88675791 | GATTATAGCTTTCTA[-/C]CCTGAGAACTGAAAT | 257632 |
rs246269630 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88668480 | TGTGTGTGTGTGTGT[G/T]TGTGTGTGTGTGTGT | 257632 |
rs246295176 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88671749 | TCAGGATGGAGTTAA[C/T]GCACGCAACGAGCTG | 257632 |
rs246300433 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88649154 | CATTTCAGTCATCGT[C/T]ATCTCACAGTTGGGA | 257632 |
rs246361812 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88648300 | CCACCCCCGCCCCCA[C/T]GCTGTGTGGAACAAA | 257632 |
rs246377179 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88680712 | TCATTTGGATGTGGT[A/T]TGAGTTGCCAGCCTG | 257632 |
rs246384430 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88677874 | CCCTTGCTCAGGAGA[C/T]ATTCAATCCAGCCCT | 257632 |
rs246425905 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88685773 | TAGCCAAGGATAAAC[G/T]CCTAATTCTTCTGCT | 257632 |
rs246552000 | in-del | -/TT | | | intron-variant | Nod2 | Mm_Celera | 8:88652156 | TGTGTGTGTATGTGT[-/TT]GTGTTGCTATCAATG | 257632 |
rs246573810 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88686498 | TATCTGCTGAGTCTG[A/G]GGTGGGGACTGAGCA | 257632 |
rs246643747 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88679238 | ACACACAGCAGAGGC[C/T]AGGCAATCCCTGCTG | 257632 |
rs246686488 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650797 | TGGAGACTCAGTCCA[C/T]GATTTGGCCCCAGCT | 257632 |
rs246721172 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88678744 | TGGGAAATTAAATTG[C/T]TCAGCGTTTCTGCCT | 257632 |
rs246778671 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661057 | GAGGCTCCGGTGACA[C/T]GGCTAAAATGTACCA | 257632 |
rs247001681 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88651896 | TCAAAAAACCAAAAA[A/C]AAACACACACAAAAA | 257632 |
rs247092761 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88674299 | ACAGCCGCAGGGGCA[C/G]GCTGTATTTTTTAAG | 257632 |
rs247143722 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88653731 | TTCAAGGTTTTGGGG[A/G]AGAGCTCCCCGATCA | 257632 |
rs247149484 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88686178 | AAAAATAATTGCATA[A/G]CCCCAAGATATGTCC | 257632 |
rs247218251 | snp | C/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88647225 | AGGCAGGCCTGTTCC[C/G]GGATACCTGTCTCAC | 257632 |
rs247374454 | in-del | -/GGT | | | intron-variant | Nod2 | Mm_Celera | 8:88672429 | AGGGATTGGGGGGAG[-/GGT]GGTTATGCTGGCGTG | 257632 |
rs247390411 | snp | A/G | | | missense | Nod2 | Mm_Celera | 8:88652927 | CTGGTGGCACTGCTG[A/G]TCTCAGGGTCCTTGG | 257632 |
rs247391218 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88668950 | TGCAGCTTGAAAACC[A/G]CTTCCCTGAGAGCCC | 257632 |
rs247455733 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88660705 | CAAAGCACAAGGCAG[C/T]TAGCGTCCATGGATG | 257632 |
rs247457715 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88668124 | AATGTTTAAGAAGGG[C/T]GGCACTATCTGTAGG | 257632 |
rs247482583 | snp | A/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645744 | AATCAAAACTGTTGG[A/G]TTTGAAACTGTTTCA | 257632 |
rs247487675 | snp | A/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646255 | TCAGTTTCTTCATCC[A/G]TAAGCCTGGGACAAG | 257632 |
rs247490640 | snp | A/G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662013 | GGCTATCGTGCCAGC[A/G/T]CTAGGTTTGTTTGGA | 257632 |
rs247500081 | in-del | -/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88677623 | TCCCCTCCCCTCTCC[-/T]CCCCCACTTCCTTCC | 257632 |
rs247537306 | snp | C/T | | | intron-variant, downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88684577 | CCAAGCCTTGGCTTT[C/T]AGATCTGTGATATGA | 257632 |
rs247562374 | in-del | -/TGTGTGTGAG | | | intron-variant | Nod2 | Mm_Celera | 8:88652169 | GTGTGTTGCTATCAA[-/TGTGTGTGAG]TGAGTGGCATACCAA | 257632 |
rs247598230 | in-del | -/CT | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88687022 | GTGGGTGACACAATC[-/CT]CTCTGGTTGCCCCGT | 257632 |
rs247781024 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88676193 | GCAGACCCTATCCCC[C/T]CTGTAAACGCTGCCA | 257632 |
rs247805662 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88653532 | TTCAAGGCCAGTGTG[A/G]TGTGACAGGATGTTT | 257632 |
rs247833860 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88667730 | AGCACCCATCCATCC[C/T]TGGAATTTTTAAATG | 257632 |
rs247872853 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661713 | AATTGGGTTTATTTA[-/T]TTTTTTAATGAAAAT | 257632 |
rs247873563 | snp | A/G | | | downstream-variant-500B | Nod2 | Mm_Celera | 8:88688593 | TTTATACCGGATAAT[A/G]TATTGCCTAATGCCA | 257632 |
rs248069068 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88666137 | CCATCCATCCCCACA[A/G]CCATGCTGGGCTCAG | 257632 |
rs248069690 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88658086 | ATTTTGGTCTTAGGA[A/C]TTAGCCTTAAGAAGT | 257632 |
rs248101571 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88680222 | GGAGTCTCCCTGCAG[A/G]TAATGTTTCAATCTC | 257632 |
rs248143933 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88674469 | TTCCAACCTATTGTG[A/G]ATCAGAGGAGAGTAG | 257632 |
rs248223399 | in-del | -/TGCCCCTGTGACCCTGCC | | | intron-variant | Nod2 | Mm_Celera | 8:88672281 | CCTTGCTAATTGCTG[-/TGCCCCTGTGACCCTGCC]TGCCTCCCTCCTGCA | 257632 |
rs248224873 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88651918 | ACACAAAAAAAAACC[C/T]GACTAAGACACCGGG | 257632 |
rs248269868 | in-del | -/AAAA | | | intron-variant | Nod2 | Mm_Celera | 8:88661681 | ATGAGACCCTCTCTC[-/AAAA]AAAAAAAAAAAGTAA | 257632 |
rs248285914 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651483 | AATGATCAAGGGGGA[A/G]GGCCCCGTGTGGGTG | 257632 |
rs248285989 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88659446 | AATGGCAGGATTTTG[C/G]GTGTTGTGGTAAAGT | 257632 |
rs248656855 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88660440 | GACTTGGGACCTTCA[G/T]ATTAGGGGTGTCCAA | 257632 |
rs248804143 | snp | A/G | | | downstream-variant-500B | Nod2 | Mm_Celera | 8:88688766 | AGGAAGAAGGCAGGT[A/G]TGTGGCTTGCCTCTG | 257632 |
rs248811104 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88652761 | GGGACAGTGCCTGAG[A/T]ACACCTGGCTCACTT | 257632 |
rs248950399 | snp | A/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645938 | AGAGGCTCTTCCCTA[A/T]ATAATCCAGACATCT | 257632 |
rs249045343 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88673884 | CTACCTCAGTCCATA[C/T]CCAATCTAATGTATT | 257632 |
rs249117957 | in-del | -/G | | | intron-variant | Nod2 | Mm_Celera | 8:88683833 | TGCCTCAAGTATAAA[-/G]GGGTAGTAACTGGCC | 257632 |
rs249161706 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88655109 | CTGGAGTCTTGGGAT[A/C]TCTGGCTTTCTTTCC | 257632 |
rs249369847 | snp | A/C/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88674850 | CTGGGGCGGAGTGGC[A/C/G]TTATGAAAGCACATG | 257632 |
rs249432918 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88675029 | TCATTGTCATGGGGG[A/G]CCGAGGGGGTTGGGG | 257632 |
rs249439860 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88669452 | TGGCTTTTGAGAGTT[G/T]AGAGTCTTGTCACAT | 257632 |
rs249517334 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88675230 | TGTGAGCTGAACCTA[C/T]CAGATAAGGACTTGT | 257632 |
rs249532703 | snp | G/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646120 | GTTATTTCATCCGCA[G/T]AAGTACTGCATAGGT | 257632 |
rs249590947 | snp | A/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645594 | TGACAAGCTAAATTC[A/G]ATCCTCAGGACCCCA | 257632 |
rs249629614 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88658120 | CTACCATCCATCCAT[A/G]TGTCCATCCATCTGT | 257632 |
rs249691097 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88660918 | AATTGCATTCTAGAC[C/T]AGACACAGATAGGGC | 257632 |
rs249721853 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88647530 | CGCTTGGTTTTGTGG[A/C]GATCACGACCGTCAC | 257632 |
rs249831755 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661466 | AATTCACTGTGTAGA[C/T]GCCACTGTGGCCCTT | 257632 |
rs249957733 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88679020 | TGGACTTAGAGGGTA[-/T]CTTTTTTTTTTTTTA | 257632 |
rs249984576 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88669830 | CCAGGCTACCAGCTC[C/T]GGGTTGGGGCTTGAG | 257632 |
rs249997248 | in-del | -/CC | | | intron-variant | Nod2 | Mm_Celera | 8:88662285 | GGCTCCAGAATGAGA[-/CC]CTGTGTCAGAAAAGA | 257632 |
rs250041036 | in-del | -/CTAT | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650516 | CAGAGACTGCCTGTG[-/CTAT]CTATGCCTCTGGGAT | 257632 |
rs250063921 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650813 | GATTTGGCCCCAGCT[C/T]ATGCTGCCCCTTGCT | 257632 |
rs250294749 | snp | A/C | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645730 | TGTAAACTATTTAAA[A/C]TCAAAACTGTTGGGT | 257632 |
rs250426927 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88682752 | CAAACAAAAGGCTCA[C/T]TTTTAGTTGGGAGGA | 257632 |
rs250525506 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88683952 | TCCTGGCCTTAATGG[G/T]AGATGTGCAACAGGC | 257632 |
rs250564965 | snp | A/G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88661829 | CATGCACGTGTACGT[A/G/T]AGTGCACGTGTGTGT | 257632 |
rs250615209 | snp | A/C | | | missense | Nod2 | Mm_Celera | 8:88665410 | CTGGCCTTTGTACTG[A/C]AACATCTCCAGCGGC | 257632 |
rs250691779 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88660057 | GTGGGTTTTGGGAGG[A/G]AGCCAGGTTGGCTGT | 257632 |
rs250727412 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658588 | TCTATCTGTCTGTTT[A/G]TCTAGTAGGAGTCCT | 257632 |
rs250761740 | snp | C/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662228 | TAATCCCAGCGCACA[C/G]TGGGGCTCAGGCAGG | 257632 |
rs250806349 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88655826 | AAGCAATGATCTAAC[G/T]TGTCTGTTAATCATT | 257632 |
rs250811194 | in-del | -/TT | | | intron-variant | Nod2 | Mm_Celera | 8:88667750 | ATTTTTAAATGGTCC[-/TT]TTTTTTTAATGATTA | 257632 |
rs250836019 | in-del | -/CTAAGCAG | | | intron-variant | Nod2 | Mm_Celera | 8:88685048 | TGAAACTTTGGTGTT[-/CTAAGCAG]CAAAGTAAAGAATAG | 257632 |
rs250903202 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88663364 | CAACTCATACCCTCC[A/C]TGGTCCCTTCAGGAG | 257632 |
rs251069653 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88667873 | GTGTCATGAAAAGTC[A/G]CTTGTTGAATTGGAG | 257632 |
rs251094893 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88683357 | TGAAGCAGCAAGTGC[C/T]GTTGGAGCACTTGGG | 257632 |
rs251184397 | in-del | -/TC | | | intron-variant | Nod2 | Mm_Celera | 8:88648342 | CCCATGCAGACCCCA[-/TC]TGTACACTGGGTGAT | 257632 |
rs251277094 | snp | A/C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88677629 | TCCCCTCTCCCCCCC[A/C/G]CTTCCTTCCTTTCTT | 257632 |
rs251304734 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88647820 | CAGGTGAGGTCCTTA[C/T]CCAGAGGGAGAAAAC | 257632 |
rs251315515 | snp | C/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88668093 | GTCCCTCAAGGGTCT[C/G]TGTGTTGGGAGGTGC | 257632 |
rs251372004 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88685482 | AGAGCAGGATGCTCT[A/G]GCTTAACACATCCTG | 257632 |
rs251425028 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650021 | GGACAGCTTCAAGCC[C/T]AGGTCTTCTTTTCCA | 257632 |
rs251427688 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88678182 | CTTTTTGTCCCCATC[C/G]CACATAACAGGCTTT | 257632 |
rs251447703 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88649608 | AGGACAGCTCAGGGC[G/T]GCATTCTGCTCTCCT | 257632 |
rs251477052 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88648551 | TGACTATCTAGGGGG[A/G]GCTAGAGAAAGCCCC | 257632 |
rs251500811 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88648694 | GGGGTGGATGGTGGG[C/T]GGCAAGGAGGAAAGG | 257632 |
rs251509482 | in-del | -/TGTT | | | intron-variant | Nod2 | Mm_Celera | 8:88669614 | TTATGTTTTTGTTGC[-/TGTT]TGTTTGTTTGTTTTG | 257632 |
rs251603198 | snp | A/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646386 | agggagtatctatta[A/G]cataccaaagcacca | 257632 |
rs251613594 | in-del | -/AG | | | intron-variant | Nod2 | Mm_Celera | 8:88658705 | ATAGCAGAAGCAAGC[-/AG]ATTGCAGAGTTTGGA | 257632 |
rs251648857 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88680198 | TGAATTGTTTACCTT[C/T]TTGCTTAAGGAGTCT | 257632 |
rs251867121 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651335 | TTGCCTGTGCTCTTT[C/T]GCTTTCCTTTTCTCC | 257632 |
rs251971362 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88685858 | CCCCGTTCCCAGAGT[C/T]AGACATTTAAGCAGA | 257632 |
rs251996706 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88663008 | GACATAGCCTTTGAG[A/T]CCTATCCTCAATGAA | 257632 |
rs252061565 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88671054 | TATACACTGAATCTG[C/T]GCTAACTGTCACAGC | 257632 |
rs252193981 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88653606 | TCCCCTTTCTTTTCT[G/T]TTTCTTGTTTGCAGT | 257632 |
rs252380281 | snp | C/T | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88686703 | AGACTCTTGTTGTGA[C/T]GTCTCCGTTTGTGAG | 257632 |
rs252399328 | snp | C/T | | | utr-variant-3-prime | Nod2 | GRCm38.p3 | 8:88687564 | TTCTTTTCTAGACTC[C/T]AAGCACTGGATGAGC | 257632 |
rs252403408 | in-del | -/ACAG | | | downstream-variant-500B | Nod2 | Mm_Celera | 8:88688880 | GCTCCCTGCTTCCGT[-/ACAG]ACAGGTTCTTTGGTG | 257632 |
rs252519273 | in-del | -/TCCA | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658401 | CCACCCACCCACCTG[-/TCCA]TCCATCCATCCATCC | 257632 |
rs252532025 | in-del | -/AGGG | | | intron-variant | Nod2 | Mm_Celera | 8:88680134 | TTTGTTTATGGTGGC[-/AGGG]AGGGGCCTAGTGAAT | 257632 |
rs252634434 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88674443 | TGGATGGGTCAGAAC[G/T]TGAGGACTATTTCCA | 257632 |
rs252697170 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88657752 | CTCCTGCCTGTGGTA[A/G]AGGTATGATTGTAGA | 257632 |
rs252748684 | snp | A/G | | | synonymous-codon | Nod2 | Mm_Celera | 8:88664914 | TGTCAGTGCTGACAC[A/G]TCGGTGGCCTCTCTC | 257632 |
rs252751092 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88676511 | ACTCAAAGACAGCTG[C/T]ATCACCAAAACGCAC | 257632 |
rs252766291 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88659617 | ACAGGATGTGCTGAC[A/G]ATGTGCAGAGAAGGG | 257632 |
rs252780411 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88675563 | TGCCTAGCCTCGTCC[A/G]TGGAAGGCTGTGTGG | 257632 |
rs252828290 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88667118 | GCTTTAGGAAGGGAT[A/G]CATCTGAGGTAAGAA | 257632 |
rs252935401 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88680674 | AAAGGAAATAACTAG[C/T]TGGCAATGGCTCTCC | 257632 |
rs252993438 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88674711 | GGTGGATTCCCCCTC[A/G]CCAAGGGGTGGGTCC | 257632 |
rs253059852 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88669647 | TTTGGTTCATAGTGT[G/T]TTATCACAGCAATGG | 257632 |
rs253067722 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88687331 | ccctttctcctccct[C/T]cctccctccctccct | 257632 |
rs253082921 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88659830 | GGTCCCAGACTCAGA[A/G]CATAGTTTAGGCTGG | 257632 |
rs253096515 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88651686 | TATAAGCTGAATAAA[C/T]CCTTTCCTCCCCAAC | 257632 |
rs253185008 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661349 | GAAGGGACTATCATT[C/T]TGGCCTTGCCTTCTG | 257632 |
rs253205915 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88651755 | CTGACTAAGAGTGGG[C/T]GTGGTGGCACATGCC | 257632 |
rs253240270 | snp | C/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646428 | GGCCTCCAGGCTCCC[C/T]CATAACCTGTAGCTC | 257632 |
rs253274767 | snp | A/T | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88651518 | CATCTCTGGGCTGGT[A/T]GTATTGGGTTCTATA | 257632 |
rs253326562 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651107 | TGGAGTTAACATCCC[C/T]AGGGCTTCCAGTGAG | 257632 |
rs253422283 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88687325 | AAGTTCCCTTTCTCC[-/T]TCCCTCCCTCCCTCC | 257632 |
rs253481794 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88681261 | TGTACCCATGACTGC[C/T]GTGTGTCACTTGGCC | 257632 |
rs253587510 | in-del | -/GC | | | intron-variant | Nod2 | Mm_Celera | 8:88668516 | TGTGTGTGCGCGCGT[-/GC]GTGCTCTCGCGAGTG | 257632 |
rs253668640 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88677045 | CACACTGGTTTAGAG[A/G]GCAGTTGGACATGCA | 257632 |
rs253752469 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88665997 | CCACGGGCCAGTCTG[A/G]TGGAAGCAATTCCTC | 257632 |
rs253882974 | in-del | -/TCCCCC | | | intron-variant | Nod2 | GRCm38.p3 | 8:88674703 | ATCCCTGAGGTGGAT[-/TCCCCC]TCGCCAAGGGGTGGG | 257632 |
rs253920182 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88674131 | AATACTTGGCCCAAA[A/G]GACACTTACCCCAGG | 257632 |
rs253981117 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88673700 | TGGGCATATTTCAGA[C/T]CAGTATGAGCTCATT | 257632 |
rs253998667 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88679035 | tcttttttttttttt[A/T]aatcacttttactgt | 257632 |
rs254003089 | in-del | -/TTAT | | | intron-variant | Nod2 | Mm_Celera | 8:88661775 | TTTCATTTTGCCTAC[-/TTAT]TTTTTTTAATTTGTG | 257632 |
rs254158055 | in-del | -/ATCCATCCATCC | | | intron-variant | Nod2 | Mm_Celera | 8:88658221 | ATCTATCCCACATCT[-/ATCCATCCATCC]ATCCATCCATCCATC | 257632 |
rs254364915 | snp | A/G | | | intron-variant, downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88684738 | CAAATAGTAGTATTG[A/G]GTGTGGTGGTGTATA | 257632 |
rs254403166 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88654396 | GGGCCCAAAGGTATG[C/T]CCCTGTGTACCTTCC | 257632 |
rs254419870 | in-del | -/TTTT | | | intron-variant | Nod2 | Mm_Celera | 8:88680924 | AGAAAGCCAGGAGGC[-/TTTT]TTTTTTTTTTTTTCC | 257632 |
rs254451158 | in-del | -/CTTTAAAGAG | | | intron-variant | Nod2 | Mm_Celera | 8:88676791 | TATTTGAGTTGTTTA[-/CTTTAAAGAG]CTTTAAAGAGCTTTC | 257632 |
rs254454291 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88661801 | AATTTGTGTGTGCCT[A/G]TATGCAAGTGTGCAT | 257632 |
rs254498011 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651208 | GGAAGGTATCAGAAT[C/T]TAACAGGAAAGACCT | 257632 |
rs254536513 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88671595 | GCAGGGACTCTGGAG[C/T]GAGGCTGTCCCCTGG | 257632 |
rs254562965 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88665896 | ctttttagtacacac[C/T]aggcccacctgtcta | 257632 |
rs254594302 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88668081 | GTGTGGATGTATGTC[C/T]CTCAAGGGTCTGTGT | 257632 |
rs254683531 | snp | C/G | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88686868 | GGAATTGACTTTTCC[C/G]GAGGAGTCGTGATGG | 257632 |
rs254764400 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88679673 | TTCTGTCGTGTCCCT[A/G]TTCAGGTGTCAGTTA | 257632 |
rs254800244 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88662062 | TAATGGCTAGAAGCT[G/T]GCATTCTAAGTCATG | 257632 |
rs254970395 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88683657 | GGATGGACACACACA[C/T]ACACACACACAGAGA | 257632 |
rs254991535 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650643 | TCCCCATAACTTCCT[-/G]GCTGTACCTCAGGCC | 257632 |
rs255002841 | in-del | -/TTTA | | | intron-variant | Nod2 | Mm_Celera | 8:88679032 | GTATCTTTTTTTTTT[-/TTTA]AATCACTTTTACTGT | 257632 |
rs255014655 | in-del | -/TTTTTTTTTTTT | | | intron-variant | Nod2 | Mm_Celera | 8:88680923 | AGAAAGCCAGGAGGC[-/TTTTTTTTTTTT]TTTTTTTTTTTTTTT | 257632 |
rs255061403 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88667940 | GGGTGGGAAGGGGGT[G/T]CCTGGGGGAATTGGG | 257632 |
rs255125744 | in-del | -/G | | | intron-variant | Nod2 | Mm_Celera | 8:88673770 | TTACGTAATCTATTT[-/G]ACAGTCACCTGTTGA | 257632 |
rs255170711 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88668525 | GCGCGTGCGTGCTCT[C/T]GCGAGTGCATGTGCA | 257632 |
rs255203899 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88657999 | TTGGAGTGGGGAAGA[A/C]ATACTTGATACTGCC | 257632 |
rs255237654 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88654515 | TGTAATTCATCACCT[G/T]TGATCTAGTGTTCAG | 257632 |
rs255247302 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88680520 | GGGTATTGAATAGCT[A/G]GGCATAAAGGAACTT | 257632 |
rs255285424 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88656515 | ATACTACATAGTGAG[G/T]GAGTTTAAGGATGGT | 257632 |
rs255377033 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88673870 | GTTCCCATAAAGCCC[C/T]ACCTCAGTCCATATC | 257632 |
rs255431534 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88647676 | GGGATGTCTCGAGGG[A/G]AGCCACGGCAGGCTT | 257632 |
rs255452314 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88651558 | GCTGAGCAAGCCAGG[A/G/T]GAAGCAAGCCAGTAA | 257632 |
rs255471761 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88649330 | GAAGTGCTCCAGGGA[A/G]GAAGGTGACAGAAAG | 257632 |
rs255674625 | snp | C/T | | | intron-variant, downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88684621 | AGGAATGGTGGAATT[C/T]TGAAGATCAGTTTTG | 257632 |
rs255748424 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88674226 | ATGAAGGGATTTATT[A/C]ATTGGTTAGCTCATT | 257632 |
rs255773548 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88665837 | AGAAGAAACAGTGGA[A/G]GGGTTCTGTTTACTG | 257632 |
rs255916034 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88672101 | TTCTGGAATGAGATG[C/G]TCATGCCTACCCTAT | 257632 |
rs256006461 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661777 | CATTTTGCCTACTTA[-/T]TTTTTTTTAATTTGT | 257632 |
rs256013389 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88670846 | CCTTGACTGCATCCA[A/G]GAAAAGGTCTCACTT | 257632 |
rs256156055 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88681089 | ATCATGCTTAGTGTA[G/T]GTCTTCGTCTCATGA | 257632 |
rs256227760 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88675337 | AATTATGTCTAAGAT[A/G]GAGGACACCCTTCAT | 257632 |
rs256301109 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88685896 | AACCGGTGGCCCTTC[C/T]TAGGTGGGCAGACTC | 257632 |
rs256367074 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88649535 | TGGGGAGCAACTCAG[A/T]CATGGGGCAGGAGAG | 257632 |
rs256441594 | in-del | -/CTCAG | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88687823 | CTGGCCGTGTCTGGA[-/CTCAG]CTCACTCTCTAAGGC | 257632 |
rs256540069 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88679623 | GCTACCTAGAGCTAG[A/G]ACCTTGCATTTGCTC | 257632 |
rs256766009 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88671552 | CTAGGTTTAGGGCCA[A/G]TCCACGGTGCTTTCA | 257632 |
rs256805670 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88679425 | TCCTGGGATTCTTCC[C/T]GTAGACACTCCTAAT | 257632 |
rs256869956 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88654464 | CTCCTGTGACCAGTA[A/G]TGGGGATAGAACCAG | 257632 |
rs256952797 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88647976 | ATGTAATCTCACCCA[C/G]GGTTGATACCCTGCA | 257632 |
rs257025353 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88655280 | AAGTGCCTTCTTTCC[C/T]CTGCTTTCTGAGCAT | 257632 |
rs257125861 | in-del | -/GGCA | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650259 | ATGGTTTGGGTATAC[-/GGCA]GGCAGGCTCTTAACA | 257632 |
rs257231842 | snp | A/G | | | intron-variant, downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88684857 | GAGGGAGGGAGGGAG[A/G]GAGAGAGAGAGGGAG | 257632 |
rs257258591 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88684412 | GTGGAAAACTAAGCC[C/T]TGTAGTAACTCATCT | 257632 |
rs257307667 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88671312 | AGACAGTGAAGAGTA[A/G]CTCCTCTTATTTCTT | 257632 |
rs257531649 | snp | A/G | | | synonymous-codon | Nod2 | Mm_Celera | 8:88686669 | GGAGGAAATCCAAAC[A/G]CTGAGCTCCAGGGAC | 257632 |
rs257632285 | snp | A/G | | | synonymous-codon | Nod2 | Mm_Celera | 8:88664332 | GCTGACCAGCCGTCC[A/G]GATGCTGTGTCAGCG | 257632 |
rs257693039 | in-del | -/TCCCT | | | intron-variant | Nod2 | Mm_Celera | 8:88652013 | TAAAACCTCTGATGG[-/TCCCT]TCCCTTCCTCACCGA | 257632 |
rs257880801 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88677292 | TGACAGTCCTCCACC[A/G]TCAAGCCTGTAATGC | 257632 |
rs257883997 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88658994 | CAATGCTAAGTGGAG[A/C]ATTCAAGGGGAGGAG | 257632 |
rs257901232 | snp | C/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88647145 | GCTTTCCTAGCTCTT[C/G]TTCCCAGGACTCTGG | 257632 |
rs257962786 | snp | C/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646302 | TGGGGTTAAGAGACT[C/T]ACTGAGAGCAGAGGC | 257632 |
rs258062758 | in-del | -/C | | | intron-variant | Nod2 | Mm_Celera | 8:88670761 | GGTGAGCCTGGACTT[-/C]CCTTCTTTTCTGAAT | 257632 |
rs258140898 | in-del | -/CTCTCTCTCTCTCTCTCTCTCT | | | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88646555 | TGTGCTCTCTCTTGG[-/CTCTCTCTCTCTCTCTCTCTCT]CTCTCTCTCTCTCTT | 257632 |
rs258191236 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88657340 | TGATATTAATGGCTG[-/T]TTTTTTATTTATATG | 257632 |
rs258201419 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88666063 | ACAACCAAGATTAGG[C/T]ATCGCAGCCAGACTT | 257632 |
rs258209540 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661983 | AGGCTTGGTATCAAG[C/T]GCTCTTACCCATTAG | 257632 |
rs258209584 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88670108 | TTATATGGGGTGACT[A/G]TCGTGGTCATTATCC | 257632 |
rs258563407 | in-del | -/TG | | | intron-variant | Nod2 | Mm_Celera | 8:88647614 | TCCTGAAAGGGACTC[-/TG]TTTCTCCTGGAAGCA | 257632 |
rs258593604 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88670061 | TTCTGACTGCTTCTG[C/T]CACAGGCCAGCTCCT | 257632 |
rs258939175 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88656766 | GCTATCTCTTTCTTA[A/C]ACCTGTTAAAGTTTC | 257632 |
rs258951324 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88675405 | CCAGTCTCTGAAGTC[C/T]GCCTCTATTCTGATT | 257632 |
rs259030576 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651566 | AGCCAGGTGAAGCAA[A/G]CCAGTAAGAAACATC | 257632 |
rs259098656 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88657714 | TTTTCTCATGGGTTT[A/G]CCAGCTTCTTCAGAT | 257632 |
rs259141912 | in-del | -/TGTGTG | | | intron-variant | Nod2 | Mm_Celera | 8:88659729 | CGTGTGTGACCAGCA[-/TGTGTG]TGTGTGTGTGTGTGT | 257632 |
rs259158613 | snp | G/T | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88688297 | CAAGGTCTTTCTGTG[G/T]TTTTTCAAAATGTCA | 257632 |
rs259180934 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651269 | ACCCCTTCTCCTCAG[C/T]ATCTTAGAATGTCCC | 257632 |
rs259253660 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88668511 | gtgtgtgtgtgtgcg[C/T]gcgtgcgtgCTCTCG | 257632 |
rs259357275 | snp | C/T | | | intron-variant, downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88684583 | CTTGGCTTTTAGATC[C/T]GTGATATGAGATGAG | 257632 |
rs259396168 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88673999 | AGGGCTCAGTTCACG[A/G]CTGTCTGGCCCCGTA | 257632 |
rs259401368 | in-del | -/TG | | | intron-variant | Nod2 | Mm_Celera | 8:88648570 | AGAGAAAGCCCCCAC[-/TG]TGTGTGTGTGTGTGT | 257632 |
rs259423647 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88658002 | GAGTGGGGAAGACAT[A/C]CTTGATACTGCCATG | 257632 |
rs259533779 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88673806 | ACTTTGGACATTTCC[A/T]GATTTTTGTTGTTGT | 257632 |
rs259692515 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88678628 | TGGGGACTTCAGACG[C/T]TGATAACAAATTGTC | 257632 |
rs259725624 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88687308 | GGTGTAAGTGAATCC[A/G]AGAAGTTCCCTTTCT | 257632 |
rs259808375 | in-del | -/TTA | | | intron-variant | Nod2 | Mm_Celera | 8:88679033 | TATCTTTTTTTTTTT[-/TTA]AATCACTTTTACTGT | 257632 |
rs259846147 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88679350 | ACTTCCATATTCACG[C/T]GGTGGACCCCACTCA | 257632 |
rs259890418 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662222 | GGCCTTTAATCCCAG[C/T]GCACACTGGGGCTCA | 257632 |
rs260116645 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88654430 | AGCATTCAAAAGCAC[A/G]TGAATAAATCCTCAG | 257632 |
rs260127997 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661230 | CTTGGGAGAAGAAGC[C/T]ACCAGTTGCAGAAGG | 257632 |
rs260188170 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88673322 | TAGGCAAGAAACAAG[A/G]CCTTACTGCCATGGA | 257632 |
rs260211293 | in-del | -/TT | | | intron-variant | Nod2 | Mm_Celera | 8:88654432 | ATTCAAAAGCACATG[-/TT]AATAAATCCTCAGTG | 257632 |
rs260211505 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88668812 | GAAACAAGAGCTTTG[G/T]GAGATGACTTCCCTC | 257632 |
rs260244686 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88662694 | TCAGAGTTAGCCTTT[C/G]AGTCTGACTAATCCA | 257632 |
rs260339964 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658340 | tccatctgtttgtcc[A/G]tctgtccacccaccc | 257632 |
rs260361972 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88685327 | ACTTCTAAATTCTGG[A/C]GGTTACACAGGGGAG | 257632 |
rs260443954 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88666414 | TCATTATGGGACTTC[C/T]GTCACTTGAGATAAA | 257632 |
rs260756287 | in-del | -/TCTGG | | | intron-variant | Nod2 | Mm_Celera | 8:88670805 | GCTGAGTTTACATGA[-/TCTGG]TCTGTGACCAATGGT | 257632 |
rs260922512 | in-del | -/C | | | intron-variant | Nod2 | Mm_Celera | 8:88678966 | GATTTTTTTCAATTT[-/C]TTTCTTTTTCTTTTC | 257632 |
rs261072472 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88659497 | CCCAATACTTGTCAC[C/T]GAGGCATGTGGCTGT | 257632 |
rs261101724 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88681374 | TGAGCTAGGAAAAAA[A/T]GAGACATTCATAATC | 257632 |
rs261220842 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88674687 | ATCACACCCCTGTGT[A/G]ATCCCTGAGGTGGAT | 257632 |
rs261271734 | snp | C/G | | | intron-variant | Nod2 | Mm_Celera | 8:88673236 | TTGCCTGTAAACTCA[C/G]TGTGAGCCAGGAGGG | 257632 |
rs261337992 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88673388 | GACATTTATGTACCA[C/T]CTAGCTTTTATGGTT | 257632 |
rs261343066 | snp | A/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646277 | TGGGACAAGAGGAGT[A/G]CCCTACAGGTGGGGT | 257632 |
rs261370311 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650305 | CTTCTGCTCTCTCAA[-/C]AGTTGTTTCTGTCTG | 257632 |
rs261371409 | snp | C/T | | | synonymous-codon | Nod2 | Mm_Celera | 8:88674918 | TAGGTTCTGGGGCAA[C/T]AGCGTGGGTGATAAG | 257632 |
rs261377558 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88683314 | CTGGGAAGGCTCCTA[A/T]TACACTGGGAAGCAT | 257632 |
rs261409642 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88682215 | CCTTTCACAGGGCTT[A/G]CCTGAGACCATCAGA | 257632 |
rs261434919 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88684388 | GCATCCTGGAACTGG[A/G]TGGGCTCAGTGGAAA | 257632 |
rs261459497 | snp | G/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646935 | AGCCTAGGAGGCTAC[G/T]TTGGAGGCAAGTGCT | 257632 |
rs261548200 | snp | A/C | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645732 | TAAACTATTTAAAAT[A/C]AAAACTGTTGGGTTT | 257632 |
rs261551890 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88653545 | TGGTGTGACAGGATG[C/T]TTCTGAGCATCCCAA | 257632 |
rs261712032 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88651902 | AACCAAAAAAAAACA[A/C]ACACAAAAAAAAACC | 257632 |
rs261810857 | snp | G/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646640 | TCTCTTCCTCTCATG[G/T]TCATGTCCCCGCTGA | 257632 |
rs261820385 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88682607 | TTCAGACATTGATTG[A/G]AAAAATATTGGCACA | 257632 |
rs261879951 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88674444 | GGATGGGTCAGAACG[C/T]GAGGACTATTTCCAA | 257632 |
rs261954374 | snp | C/G | | | missense | Nod2 | Mm_Celera | 8:88653266 | GAGCTGGCAAGGGAG[C/G]GGGGGTTTCTGAGCC | 257632 |
rs262081341 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88670092 | CTCCATCTTAACAGC[C/T]TTATATGGGGTGACT | 257632 |
rs262173787 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88647872 | AACTATTCCTGGTTC[A/G]GTTCCCCCCACCCCC | 257632 |
rs262238214 | snp | A/C | | | intron-variant | Nod2 | Mm_Celera | 8:88652729 | GTTAGCTTTTGATAT[A/C]CCAGGGCTTCACTTT | 257632 |
rs262270540 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88660474 | TTAATAGAAACCTTC[C/T]CACACTGTTCCTCTT | 257632 |
rs262304409 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88680100 | AGTCTTCTTTACTCT[G/T]CTGGGACAGAGGCCC | 257632 |
rs262324247 | snp | C/G | | | downstream-variant-500B | Nod2 | Mm_Celera | 8:88688919 | TTGCTAAATGCTGGG[C/G]CATCTCCCTGGGTGT | 257632 |
rs262433944 | in-del | -/CCAT | | | intron-variant | Nod2 | Mm_Celera | 8:88658542 | CATCCATCCATCTGC[-/CCAT]CCATCCATCCATCCA | 257632 |
rs262450021 | in-del | -/CCAC | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658313 | CTACCATCCATCCAT[-/CCAC]CCACCCATCAGTCCA | 257632 |
rs262616890 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88656352 | ATATATTCTCTCTTC[C/T]ATTTTGTAGACAATT | 257632 |
rs262723920 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88651019 | TCCAGCCTGCGTGTC[C/T]GCAATGTGGTGTTGA | 257632 |
rs262912339 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88685812 | CCAAGTGCTGGGATT[A/G]CAGGTGTGCACCGCC | 257632 |
rs262987824 | in-del | -/TGTGGT | | | intron-variant | Nod2 | Mm_Celera | 8:88656189 | GAATGTCACTGGGAA[-/TGTGGT]TTGAGGAAGTGGGGC | 257632 |
rs263090933 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88685753 | CTGGCTTCAAACTCA[C/T]TGTGTAGCCAAGGAT | 257632 |
rs263113219 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88668899 | TGCTCAGACTTTCAG[A/T]ATTGTCTGTGGAGCT | 257632 |
rs263209740 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88653552 | ACAGGATGTTTCTGA[A/G]CATCCCAAGAGCACA | 257632 |
rs263224541 | snp | C/T | | | utr-variant-3-prime | Nod2 | Mm_Celera | 8:88686939 | GAGCCGAGAGGACCG[C/T]GTTTCTGCCTCTAAA | 257632 |
rs263251878 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88663693 | TTGCCTCTTCTGTAT[C/T]CTAGCTGCTGAGTGT | 257632 |
rs263264754 | in-del | -/CCCG | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650611 | AAATGAGCCAGGCCA[-/CCCG]ATCTCAAATCTTTTC | 257632 |
rs263368717 | in-del | -/TT | | | intron-variant | Nod2 | Mm_Celera | 8:88652155 | ATGTGTGTGTATGTG[-/TT]TGTGTTGCTATCAAT | 257632 |
rs263404789 | snp | A/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88686256 | CTCTAATGTGCCTTG[A/C]TGACTCTTGATGAAG | 257632 |
rs263420407 | snp | A/T | | | intron-variant | Nod2 | Mm_Celera | 8:88658856 | aggagctgggaaaag[A/T]ctaaagtgggtgaga | 257632 |
rs263522416 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88662999 | GTAGGCCGGGACATA[A/G]CCTTTGAGTCCTATC | 257632 |
rs263575235 | in-del | -/TG | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88647068 | TGCCTCCATTAAGAC[-/TG]TAGCTGACTAAGGGC | 257632 |
rs263589889 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88680331 | CATCTCTTCTTGATA[A/G]AGAAGCACCTCATTG | 257632 |
rs263685607 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88671903 | CAGAAAATGCCCACG[A/G]GTAGTGGGAGAATGA | 257632 |
rs263693985 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88653412 | CTTGTTGAGTCAGCC[C/T]CATGGAATAATGCGG | 257632 |
rs263806674 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88658629 | CTCTGTCATTGGGAC[C/T]AAATCAGTGAATACA | 257632 |
rs263846877 | in-del | -/TCTA | | | intron-variant | Nod2 | Mm_Celera | 8:88659925 | CCAGCCTTCCAGGGG[-/TCTA]TCTATAGCTTCCAAA | 257632 |
rs263870310 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88649959 | AGGAAGGTACAAGAA[C/T]GAGATTCTGGGACTA | 257632 |
rs263935092 | in-del | -/CCA | | | intron-variant | Nod2 | Mm_Celera | 8:88659401 | AAAAAGCAGCACGTT[-/CCA]CTACTTCTTATGTTG | 257632 |
rs263982282 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88651249 | GGCCATTTCCAGCTG[C/T]CCCCACCCCTTCTCC | 257632 |
rs263984053 | in-del | -/GC | | | intron-variant | Nod2 | Mm_Celera | 8:88670265 | GGATTTTGGATGGGG[-/GC]GGGGGGTCTCTATCT | 257632 |
rs264043353 | snp | C/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88646041 | CTATTCCTTGGCATC[C/T]GTGAACCTGCTCTAG | 257632 |
rs264196416 | snp | C/T | | | missense | Nod2 | Mm_Celera | 8:88664843 | CCCGGGAGCAAGGCG[C/T]CCCTGGAGTTCCTGC | 257632 |
rs264202212 | in-del | -/CA | | | intron-variant | Nod2 | Mm_Celera | 8:88653446 | GTGGGATTTCCTGTG[-/CA]CAGTGGGCCAGGCAG | 257632 |
rs264326420 | in-del | -/C | | | intron-variant | Nod2 | Mm_Celera | 8:88677983 | ATAGCTTTTGCTTCT[-/C]TTTTTATGGCCAGCA | 257632 |
rs264331768 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88667098 | AGAGGAAGACCCAGG[A/G]AGGAGCTTTAGGAAG | 257632 |
rs264345469 | in-del | -/G | | | intron-variant | Nod2 | Mm_Celera | 8:88669147 | AATGATACTACTGTT[-/G]GGGGGGTACACAGAG | 257632 |
rs264419680 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661521 | TCAAGTATAGCTGGC[C/T]ACATAGGCATTAGAC | 257632 |
rs264455403 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88669227 | TGTACAGTGCATGGG[C/T]AGAGTTTGCTGAGGT | 257632 |
rs264616519 | in-del | -/TAACAAGCATCACCCT | | | intron-variant | Nod2 | Mm_Celera | 8:88667984 | TTGGGAACCTGTGTG[-/TAACAAGCATCACCCT]TTATTCAGACACCAG | 257632 |
rs264671549 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88652576 | CGTGCTCTCTGGTGG[A/G]ACTCGTCACCCTGCC | 257632 |
rs264831458 | in-del | -/TTT | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645303 | TTATTGGCAATAGGC[-/TTT]TTTTTTTATTGATAG | 257632 |
rs264916246 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88670217 | GGGTCCCCAGTCCTT[A/G]GACTGTCCTCTATCA | 257632 |
rs264934091 | snp | A/G | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88647216 | AAGCACTGCAGGCAG[A/G]CCTGTTCCCGGATAC | 257632 |
rs264967975 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88686088 | CCATTGCTGGTGAGG[C/T]CCAGTAGCCTAGCAT | 257632 |
rs265067168 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88681026 | GAGCTGGAATGATGT[C/T]GACAGCAGGTTACCA | 257632 |
rs265090720 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88683358 | GAAGCAGCAAGTGCT[G/T]TTGGAGCACTTGGGG | 257632 |
rs265109598 | in-del | -/TGTGTG | | | intron-variant | Nod2 | Mm_Celera | 8:88648569 | AGAGAAAGCCCCCAC[-/TGTGTG]TGTGTGTGTGTGTGT | 257632 |
rs265123151 | in-del | -/GG | | | intron-variant | Nod2 | Mm_Celera | 8:88662743 | CAGACATGGGGGGCC[-/GG]GGGGGGGCGTCTGGG | 257632 |
rs265145465 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88653575 | AGAGCACATGTCAAG[C/T]GCTTCATCTGTTCCT | 257632 |
rs265324104 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650035 | CCAGGTCTTCTTTTC[A/C]AGCTCTTTGGGATGA | 257632 |
rs265427358 | in-del | -/TT | | | intron-variant | Nod2 | Mm_Celera | 8:88681527 | TTATGCATGTTGGGA[-/TT]TTTTTTTTAAAAAGA | 257632 |
rs265489397 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661826 | GTGCATGCACGTGTA[C/T]GTAAGTGCACGTGTG | 257632 |
rs265529091 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88651763 | GAGTGGGCGTGGTGG[C/T]ACATGCCTTTAATCC | 257632 |
rs265558611 | snp | C/T | | | intron-variant | Nod2 | Mm_Celera | 8:88663152 | AAGCCTTAATAGTCC[C/T]TGTTTCTACAGCTAA | 257632 |
rs265706839 | in-del | -/TCTA | | | intron-variant | Nod2 | Mm_Celera | 8:88658573 | CCATCCATCCATCTG[-/TCTA]TCTGTCTGTTTATCT | 257632 |
rs265990492 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88652155 | TATGTGTGTGTATGT[G/T]TGTGTTGCTATCAAT | 257632 |
rs266017464 | in-del | -/TGCACC | | | intron-variant | Nod2 | Mm_Celera | 8:88675629 | TTTGGCTTTGAGTCG[-/TGCACC]TGCGCCTGCAGACCC | 257632 |
rs266166771 | snp | A/G | | | intron-variant | Nod2 | Mm_Celera | 8:88666314 | CTGGGGAATCCTTGA[A/G]GTCCCACACAAAGTT | 257632 |
rs266218573 | snp | G/T | | | intron-variant | Nod2 | Mm_Celera | 8:88660389 | TGTTGTGACATTGTG[G/T]CAGCACTTAGAATGG | 257632 |
rs386863121 | in-del | -/TTTT | | | intron-variant | Nod2 | Mm_Celera | 8:88680940 | TTTTTTTTTTTTTTT[-/TTTT]CCATCTGTGAGGCTT | 257632 |
rs386863215 | in-del | -/CT | | | intron-variant | Nod2 | Mm_Celera | 8:88656939 | CCTTTTCTTCTCTCT[-/CT]ATGGAATTGCAGCTG | 257632 |
rs386911613 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88677988 | TTTTGCTTCTTTTTT[-/T]ATGGCCAGCACCCAA | 257632 |
rs386912165 | in-del | -/GTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCGC | | | intron-variant | Nod2 | Mm_Celera | 8:88668476 | TGTGTGTGTGTGTGT[lengthTooLong]GTGCGTGCTCTCGCG | 257632 |
rs386932787 | in-del | -/ATCT | | | intron-variant | Nod2 | Mm_Celera | 8:88658576 | TCCATCCATCTGTCT[-/ATCT]GTCTGTTTATCTAGT | 257632 |
rs386945551 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88679011 | ACTGAAGGTTGGACT[-/T]AGAGGGTATCTTTTT | 257632 |
rs386960001 | in-del | -/AACAAGCATCACCCTT | | | intron-variant | Nod2 | Mm_Celera | 8:88667985 | TGGGAACCTGTGTGT[-/AACAAGCATCACCCTT]TATTCAGACACCAGA | 257632 |
rs387031830 | snp | A/G | | | intron-variant, downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88684853 | GAGAGAGGGAGGGAG[A/G]GAGGGAGAGAGAGAG | 257632 |
rs387045422 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661785 | CTACTTATTTTTTTT[-/T]AATTTGTGTGTGCCT | 257632 |
rs387152997 | in-del | -/C | | | intron-variant | Nod2 | Mm_Celera | 8:88675793 | TTATAGCTTTCTACC[-/C]TGAGAACTGAAATCC | 257632 |
rs387159282 | in-del | -/AGG | | | intron-variant | Nod2 | Mm_Celera | 8:88672428 | GTAGGGATTGGGGGG[-/AGG]GTTATGCTGGCGTGT | 257632 |
rs387166387 | in-del | -/TGGCACTGGCCT | | | intron-variant | Nod2 | Mm_Celera | 8:88655316 | GGGAAAGTGTGCACT[-/TGGCACTGGCCT]AGTGTTCTCTCTAGT | 257632 |
rs387167146 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88649666 | GCTGGAGGCCTGGGG[-/G]CACTGCAAAGGGATT | 257632 |
rs387204122 | in-del | -/C | | | intron-variant | Nod2 | Mm_Celera | 8:88678685 | TTGGGGACGGACTTC[-/C]CTCATAATGTCTTGG | 257632 |
rs387223350 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88657346 | TAATGGCTGTTTTTT[-/T]ATTTATATGATTAGT | 257632 |
rs387236262 | in-del | -/AAAAAAC | | | intron-variant | Nod2 | Mm_Celera | 8:88651916 | CACACAAAAAAAAAC[-/AAAAAAC]CTGACTAAGACACCG | 257632 |
rs387237416 | in-del | -/TTGTGCATGTGT | | | intron-variant | Nod2 | Mm_Celera | 8:88661844 | AGTGCACGTGTGTGT[-/TTGTGCATGTGT]GTGTGTGTGTGTGTG | 257632 |
rs387280071 | in-del | -/TTCCT | | | intron-variant | Nod2 | GRCm38.p3 | 8:88678578 | GTAATATTTGCTCCT[-/TTCCT]CCTCTGTGGTCATCC | 257632 |
rs387283549 | in-del | -/CACACACACACACA | | | intron-variant | Nod2 | Mm_Celera | 8:88683656 | GGATGGACACACACA[-/CACACACACACACA]TACACACACACAGAG | 257632 |
rs387299148 | in-del | -/GA | | | intron-variant | Nod2 | Mm_Celera | 8:88658706 | TAGCAGAAGCAAGCA[-/GA]TTGCAGAGTTTGGAA | 257632 |
rs387461621 | in-del | -/AGGC | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650266 | GGGTATACGGCAGGC[-/AGGC]TCTTAACATATCTGG | 257632 |
rs387477665 | in-del | -/A | | | intron-variant | Nod2 | Mm_Celera | 8:88655965 | AACTAAGAAAAAAAA[-/A]TAAGCATACTTTTGT | 257632 |
rs387479172 | in-del | -/C | | | intron-variant | Nod2 | Mm_Celera | 8:88678686 | TGGGGACGGACTTCC[-/C]TCATAATGTCTTGGG | 257632 |
rs387500229 | in-del | -/CCCCTC | | | intron-variant | Nod2 | GRCm38.p3 | 8:88674705 | CCCTGAGGTGGATTC[-/CCCCTC]GCCAAGGGGTGGGTC | 257632 |
rs387507015 | snp | A/G | | | intron-variant, downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88684894 | AGAGAGAGAGAGAGG[A/G]AGAGGGAGAGAAGGA | 257632 |
rs387513533 | in-del | -/G | | | intron-variant | Nod2 | Mm_Celera | 8:88670362 | CTCCTTGGGGGGGGG[-/G]TTGTCTCATCAGCTC | 257632 |
rs387515448 | in-del | -/GAT | | | intron-variant | Nod2 | Mm_Celera | 8:88680221 | GGAGTCTCCCTGCAG[-/GAT]ATGTTTCAATCTCAG | 257632 |
rs387544809 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88667758 | ATGGTCCTTTTTTTT[-/T]AATGATTAAGAACGT | 257632 |
rs387576974 | in-del | -/CGCGCG | | | intron-variant | Nod2 | GRCm38.p3 | 8:88668509 | GTGTGTGTGTGTGTG[-/CGCGCG]TGCGTGCTCTCGCGA | 257632 |
rs387632711 | in-del | -/GCGCGC | | | intron-variant | Nod2 | Mm_Celera | 8:88669348 | ACACACACACACACG[-/GCGCGC]AATAGGGGCAGGTAT | 257632 |
rs387640304 | in-del | -/AAAGAGCTTT | | | intron-variant | Nod2 | Mm_Celera | 8:88676805 | ACTTTAAAGAGCTTT[-/AAAGAGCTTT]CCTGTAGGATGGAAT | 257632 |
rs387668220 | in-del | -/GG | | | downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88688556 | TTTAAAGTACCACAA[-/GG]GGGGGGGGGGACAAT | 257632 |
rs387683380 | in-del | -/T | | | intron-variant | Nod2 | Mm_Celera | 8:88661719 | GTTTATTTATTTTTT[-/T]AATGAAAATGAGAGA | 257632 |
rs387691389 | in-del | -/CTTCC | | | intron-variant | Nod2 | Mm_Celera | 8:88652021 | CTGATGGTCCCTTCC[-/CTTCC]TCACCGAGTCCCCAG | 257632 |
rs387728760 | in-del | -/GGGAGTCTG | | | intron-variant | Nod2 | Mm_Celera | 8:88686347 | CAATAGCTGGCCTTG[-/GGGAGTCTG]TAGCTGGCCTGGCCC | 257632 |
rs387743499 | in-del | -/G | | | intron-variant | Nod2 | Mm_Celera | 8:88670353 | GGTGAGGGTCTCCTT[-/G]GGGGGGGGGTTGTCT | 257632 |
rs387746059 | in-del | -/GGGGGG | | | intron-variant | Nod2 | Mm_Celera | 8:88675545 | GTGAGTTATGGGGGG[-/GGGGGG]TTTGCCTAGCCTCGT | 257632 |
rs387760654 | in-del | -/CCTGTGACCCTGCCTGCC | | | intron-variant | Nod2 | Mm_Celera | 8:88672285 | GCTAATTGCTGTGCC[-/CCTGTGACCCTGCCTGCC]TCCCTCCTGCAGTAT | 257632 |
rs387766799 | in-del | -/T | | | upstream-variant-2KB | Nod2 | Mm_Celera | 8:88645310 | GCAATAGGCTTTTTT[-/T]ATTGATAGGCAATGC | 257632 |
rs387803502 | snp | A/G | | | intron-variant, downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88684849 | AACAGAGAGAGGGAG[A/G]GAGGGAGGGAGAGAG | 257632 |
rs387835103 | in-del | -/CATCCATCCATC | | | intron-variant | Nod2 | Mm_Celera | 8:88658236 | ATCCATCCATCCATC[-/CATCCATCCATC]TACCCATCCATTCAT | 257632 |
rs387843320 | in-del | -/CTAT | | | intron-variant, upstream-variant-2KB | Nod2 | Mm_Celera | 8:88650520 | GACTGCCTGTGCTAT[-/CTAT]GCCTCTGGGATTTTT | 257632 |
rs387869570 | in-del | -/G | | | intron-variant | Nod2 | Mm_Celera | 8:88669153 | ACTACTGTTGGGGGG[-/G]TACACAGAGCAGTGC | 257632 |
rs578337125 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88651537 | TTGGGTTCTATAAGA[A/G]AGCAGGCTGAGCAAG | 257632 |
rs578344128 | snp | A/G | | | intron-variant, downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88684870 | AGGGAGAGAGAGAGG[A/G]AGAGAGAGAGAGAGA | 257632 |
rs578421738 | snp | A/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658302 | CCACCCATCTATCTA[A/C]CATCCATCCATCCAC | 257632 |
rs578832117 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88668447 | AAGAGGTTAGCATTT[C/T]GTGTGTGTGTGTGTG | 257632 |
rs578854226 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88651579 | AAGCCAGTAAGAAAC[A/G]TCCCTCCATGGCCTC | 257632 |
rs578942263 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658564 | TCCATCCATCCATCC[A/G]TCCATCTGTCTATCT | 257632 |
rs578951586 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88677583 | CTTCTCCTCTCCCCT[C/T]TCCCTCCCCTCCCCT | 257632 |
rs579019529 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88668873 | GCTGTCCTATTTCAG[C/T]GTTGACATCCTGCTC | 257632 |
rs579034643 | snp | A/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88683706 | GAGAGAGAGAGAGAG[A/T]GAGAGGATGCTCTCC | 257632 |
rs579415136 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88655922 | AGAAAGAAAGAGAGA[A/G]AGAAAAGAAAGGAAG | 257632 |
rs579513213 | snp | A/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88651889 | CCCTGTCTCAAAAAA[A/C]CAAAAAAAAACACAC | 257632 |
rs579545693 | snp | A/C/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88669350 | CACACACACACACGC[A/C/G]CGCCAATAGGGGCAG | 257632 |
rs579610081 | snp | G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88682789 | GGAACCATGGGTGTG[G/T]GTGTGTGTGTGTGTG | 257632 |
rs579629293 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88659981 | TAGGTTTATGTATTT[A/G]TTTGGTCTTTTTTTT | 257632 |
rs580113974 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88682852 | CGGCAGTCCCAAAGG[C/T]GCCAGAGACTGCAGC | 257632 |
rs580264469 | snp | G/T | | | intron-variant, utr-variant-5-prime | Nod2 | GRCm38.p3 | 8:88651663 | GTGATCAACAGCAAT[G/T]TGGAAGGTATAAGCT | 257632 |
rs580295392 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658701 | AGATCATAGCAGAAG[C/T]AAGCATTGCAGAGTT | 257632 |
rs580380469 | snp | C/T | | | upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88646579 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTTCTC | 257632 |
rs580410698 | snp | C/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88682859 | CCCAAAGGCGCCAGA[C/G]ACTGCAGCTAAGTCA | 257632 |
rs580644109 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88655928 | AAAGAGAGAAAGAAA[A/G]GAAAGGAAGGAAGAA | 257632 |
rs580736448 | snp | A/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88682943 | CAGGTGTACCAGGAT[A/T]CAGGTGAATCCAATT | 257632 |
rs580810516 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88648581 | CCACTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 257632 |
rs580820309 | snp | C/T | | | utr-variant-3-prime | Nod2 | GRCm38.p3 | 8:88687035 | TCCTCTCTGGTTGCC[C/T]CGTGGGAGGAAGATG | 257632 |
rs580913662 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88675632 | TGGCTTTGAGTCGTG[C/T]GCCTGCAGACCCTGG | 257632 |
rs580929116 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88667973 | AGTTGGGGAGGGTTG[A/G]GAACCTGTGTGTTAT | 257632 |
rs580944764 | snp | G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88652133 | AGCAAGGGCCTTCCG[G/T]CAAGGGTATGTGTGT | 257632 |
rs581223676 | snp | A/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88649196 | GGGCAGAGACGCATC[A/C]GTGATTTGTACTTGG | 257632 |
rs581296108 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88683012 | CTGCGTGCCTGGTGA[A/G]GTGGCGTGGCCTGCT | 257632 |
rs581329142 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662274 | AGGCAAGTCTGGGCT[C/T]CAGAATGAGACCCTG | 257632 |
rs581440840 | snp | A/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88654831 | AGTGGGGGTCAGATG[A/C]CTTTAATCCAGCACT | 257632 |
rs581554234 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650633 | AATCTTTTCATTCCC[C/T]ATAACTTCCTGCTGT | 257632 |
rs581869819 | snp | A/G | | | intron-variant, downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88684877 | GAGAGAGGGAGAGAG[A/G]GAGAGAGAGAGAGAG | 257632 |
rs582079026 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88669603 | ATCTCGATTCTATTA[C/T]GTTTTTGTTGCTGTT | 257632 |
rs582082445 | snp | G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88668472 | TGTGTGTGTGTGTGT[G/T]TGTGTGTTTGTGTGT | 257632 |
rs582100385 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88682829 | GTGTGTGTGGGGAGC[A/G]GGTGTGGCGGCAGTC | 257632 |
rs582178063 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658350 | TGTCCGTCTGTCCAC[C/T]CACCCACCCATTCAT | 257632 |
rs582287655 | snp | G/T | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88651604 | GGCCTCTGCATCAGC[G/T]CCTGCTTCCTGACCT | 257632 |
rs582316079 | snp | A/G | | | intron-variant, downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88684913 | GGGAGAGAAGGAAGA[A/G]GAAGAAGAAGAAGAA | 257632 |
rs582695384 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658567 | ATCCATCCATCCATC[C/T]ATCTGTCTATCTGTC | 257632 |
rs582704609 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88669139 | GTGAAATTAATGATA[C/T]TACTGTTGGGGGGGT | 257632 |
rs583047776 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685831 | GTGTGCACCGCCATG[C/T]CTGGCTTGGAGCCCC | 257632 |
rs583217567 | snp | G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88671335 | TATTTCTTGCCTGCT[G/T]GCTGCCTTTGGAATG | 257632 |
rs583225510 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88651983 | CTATTTCTCTGCCGC[A/G]TAGGATCTTAGTGCC | 257632 |
rs583227131 | snp | G/T | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650974 | TAGCTTCGCTGCCTC[G/T]GCTTTTCCCTGTCTG | 257632 |
rs583328116 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88682961 | GGTGAATCCAATTTG[A/G]TGGAGATTTGCCCCT | 257632 |
rs583500825 | snp | A/T | | | utr-variant-3-prime | Nod2 | GRCm38.p3 | 8:88687729 | GAAAGCATGGATGTT[A/T]ACTGAACGCCTGTTG | 257632 |
rs583622674 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88682855 | CAGTCCCAAAGGCGC[C/T]AGAGACTGCAGCTAA | 257632 |
rs583783621 | snp | A/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88659409 | GCACGTTCCACTACT[A/T]CTTATGTTGACCGTG | 257632 |
rs583798132 | snp | A/C/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662742 | CACAGACATGGGGGG[A/C/G]CGGGGGGGCGTCTGG | 257632 |
rs583971769 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88684994 | AGAAGAAGAAGAGAG[A/G]AAGGAAAGTATAAAA | 257632 |
rs583975897 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88651672 | AGCAATGTGGAAGGT[A/G]TAAGCTGAATAAACC | 257632 |
rs584044715 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nod2 | GRCm38.p3 | 8:88650242 | TCATTGCCTGGGTGT[A/G]GATGGTTTGGGTATA | 257632 |
rs584063599 | snp | A/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88648198 | AGCATTGTAGGGTGG[A/C]CCAGTGAGCAGACGC | 257632 |
rs584092915 | snp | A/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88682915 | ATAAGACACAAACAT[A/C]TTGAGTGATGCGCAG | 257632 |
rs584102855 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88657326 | TAATGTAGACAAGAT[A/G]ATATTAATGGCTGTT | 257632 |
rs584281373 | snp | G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88648606 | GTGTGTGTGTGTAGG[G/T]AGGGAGGGAGGAGCT | 257632 |
rs584718322 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88668850 | CTGACTCACCCTGCT[C/T]TCTTTCAGCTGTCCT | 257632 |
rs584800910 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88683017 | TGCCTGGTGAGGTGG[C/T]GTGGCCTGCTGTGCG | 257632 |
rs584807226 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88649218 | TGTACTTGGGGGTGG[A/G]GTGGGGGACTAGGAA | 257632 |
rs584832726 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88655921 | AAGAAAGAAAGAGAG[A/G]AAGAAAAGAAAGGAA | 257632 |
rs585227446 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88680146 | TGGCAGGGGCCTAGT[A/G]AATCTAGTCTGTTTC | 257632 |
rs585332540 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88659716 | GAAAGGCGTGTGTGC[A/G]TGTGTGACCAGCATG | 257632 |
rs585433977 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88682778 | GAGGAGGATGTGGAA[C/T]CATGGGTGTGTGTGT | 257632 |
rs585489710 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88682846 | GTGTGGCGGCAGTCC[C/T]AAAGGCGCCAGAGAC | 257632 |
rs585736817 | snp | A/G | | | intron-variant, downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88684878 | AGAGAGGGAGAGAGA[A/G]AGAGAGAGAGAGAGG | 257632 |
rs585845341 | snp | A/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658498 | CCACCCAGCCACTCA[A/T]GTATCCAACCATCCA | 257632 |
rs585955085 | snp | C/G | | | intron-variant, utr-variant-5-prime | Nod2 | GRCm38.p3 | 8:88651653 | ACTTCCTTTGGTGAT[C/G]AACAGCAATGTGGAA | 257632 |
rs585975027 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658571 | ATCCATCCATCCATC[C/T]GTCTATCTGTCTGTT | 257632 |
rs585992332 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88684967 | AGAAGAAGAAGAAGA[A/G]GAAGAAGAAGAAGAA | 257632 |
rs586056862 | snp | A/C/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88669348 | CACACACACACACAC[A/C/G]CGCGCCAATAGGGGC | 257632 |
rs586151680 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88648349 | AGACCCCATCTGTAC[A/G]CTGGGTGATGCACAG | 257632 |
rs586444123 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88651688 | TAAGCTGAATAAACC[C/T]TTTCCTCCCCAACTG | 257632 |
rs586465475 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685044 | TATTCTGAAACTTTG[A/G]TGTTCAAAGTAAAGA | 257632 |
rs586556204 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88667029 | CAGAGTTGTGGGTGG[A/G]AATTAGGAAGGGCTC | 257632 |
rs586557333 | snp | G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88658835 | GAGTATTCTCAGTGA[G/T]AAGATAGGAGCTGGG | 257632 |
rs586570276 | snp | A/C | | | intron-variant | Nod2 | GRCm38.p3 | 8:88682923 | CAAACATCTTGAGTG[A/C]TGCGCAGGTGTACCA | 257632 |
rs586645654 | snp | C/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88685840 | GCCATGCCTGGCTTG[C/G]AGCCCCGTTCCCAGA | 257632 |
rs586656448 | snp | A/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88682969 | CAATTTGGTGGAGAT[A/T]TGCCCCTGCTGCCCT | 257632 |
rs586825885 | snp | C/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88662743 | ACAGACATGGGGGGC[C/G]GGGGGGGCGTCTGGG | 257632 |
rs587126995 | snp | G/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88672436 | TGGGGGGAGGGTTAT[G/T]CTGGCGTGTACACTG | 257632 |
rs587230126 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88682858 | TCCCAAAGGCGCCAG[A/G]GACTGCAGCTAAGTC | 257632 |
rs587264718 | snp | G/T | | | downstream-variant-500B | Nod2 | GRCm38.p3 | 8:88688865 | GCTGCTGGCCACAGT[G/T]GCTCCCTGCTTCCGT | 257632 |
rs587269901 | snp | A/G | | | intron-variant | Nod2 | GRCm38.p3 | 8:88653435 | TAATGCGGTTGGTGG[A/G]ATTTCCTGTGCACAG | 257632 |
rs587570864 | snp | C/T | | | intron-variant | Nod2 | GRCm38.p3 | 8:88654824 | AGAATGAAGTGGGGG[C/T]CAGATGCCTTTAATC | 257632 |