SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3684502 | snp | C/T | 0.5 | 0 | intron-variant | Snx9 | GRCm38.p3 | 17:5899534 | AGCAAGATCAGCCTA[C/T]GCCCCCTGCCTGTCA | 66616 |
rs3686322 | snp | G/T | 0.5 | 0 | intron-variant | Snx9 | GRCm38.p3 | 17:5899228 | GAGACTTAGAGGAAA[G/T]CACAATCAGCCTACT | 66616 |
rs3686338 | snp | A/G | 0.5 | 0 | intron-variant | Snx9 | GRCm38.p3 | 17:5899224 | CTTAGAGGAAAGCAC[A/G]ATCAGCCTACTCCCC | 66616 |
rs3692285 | snp | A/G | 0.5 | 0 | intron-variant | Snx9 | GRCm38.p3 | 17:5888866 | GGCTGCAAATACTAT[A/G]GGTTTAGCATATAGG | 66616 |
rs3694565 | snp | A/C/G | 0.35124 | 0.228584 | intron-variant | Snx9 | GRCm38.p3 | 17:5885430 | GCAAAGCGATGGGTG[A/C/G]AAACTGCTTCGCACT | 66616 |
rs3694705 | snp | A/C/T | 0.429688 | 0.173817 | intron-variant | Snx9 | GRCm38.p3 | 17:5885354 | GCCCTTCAAAGCTCA[A/C/T]GTTCAGCCATCACCC | 66616 |
rs6169874 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Snx9 | GRCm38.p3 | 17:5912150 | TAGCTATGACTTTGC[A/G]TGGTATTTTATGCTT | 66616 |
rs6172158 | snp | C/T | 0.5 | 0 | intron-variant | Snx9 | GRCm38.p3 | 17:5911718 | GCCGCCTTTTAAAAC[C/T]GCTTAGTGTGGAGGG | 66616 |
rs6253312 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Snx9 | GRCm38.p3 | 17:5895154 | CCAGGAAGTGCTCAA[A/G]GTCTGCAGAGGAACA | 66616 |
rs6255006 | snp | C/G | 0.5 | 0 | intron-variant | Snx9 | Mm_Celera | 17:5894844 | tcagcaaggtaaaat[C/G]acaaagtctggcatc | 66616 |
rs6255579 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Snx9 | Mm_Celera | 17:5894724 | CAAGGGAGCACTCCT[C/G]TTTGTGGATGGAGAG | 66616 |
rs6357443 | snp | C/T | 0.5 | 0 | intron-variant | Snx9 | GRCm38.p3 | 17:5909837 | AAGATGATTTGTGGT[C/T]CCTCCCTAAGTCCCT | 66616 |
rs6358406 | snp | A/C | 0.5 | 0 | intron-variant | Snx9 | GRCm38.p3 | 17:5909690 | AAGCCTGACTCTCCC[A/C]CTCAGTCCACTGCCC | 66616 |
rs6371602 | snp | C/T | 0.5 | 0 | intron-variant | Snx9 | GRCm38.p3 | 17:5909514 | GAGGACACTCAGCTC[C/T]GCCATGCCNAGTTTC | 66616 |
rs6371614 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Snx9 | GRCm38.p3 | 17:5909505 | CAGCTCCGCCATGCC[A/G]AGTTTCTGAGAGCAG | 66616 |
rs6371977 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Snx9 | GRCm38.p3 | 17:5909498 | GCCATGCCAAGTTTC[C/T]GAGAGCAGAGGCAAA | 66616 |
rs6372075 | snp | A/G | 0.5 | 0 | intron-variant | Snx9 | GRCm38.p3 | 17:5909441 | GATTGCTTAGCAGCA[A/G]GTTGTTCATTTGTAA | 66616 |
rs6372634 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Snx9 | GRCm38.p3 | 17:5909306 | GAAATTGCAAAGTGT[C/T]CATCACAAGTGCTAG | 66616 |
rs6389371 | snp | A/G | 0.5 | 0 | intron-variant | Snx9 | GRCm38.p3 | 17:5908513 | GGAGAAAGGGCCAGC[A/G]GCAGCCAGCTTNGTT | 66616 |
rs6389795 | snp | C/T | 0.5 | 0 | intron-variant | Snx9 | GRCm38.p3 | 17:5908501 | AGCNGCAGCCAGCTT[C/T]GTTCTGAGAGCAGAT | 66616 |
rs6389906 | snp | A/G | 0.46875 | 0.121031 | synonymous-codon | Snx9 | GRCm38.p3 | 17:5908440 | GTAGCTCTTCAGACC[A/G]TACATTTTGGAACCT | 66616 |
rs6390880 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Snx9 | GRCm38.p3 | 17:5908290 | AACACAGGCGCAACA[A/G]GGGAGAGAAATTCCG | 66616 |
rs6390940 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Snx9 | GRCm38.p3 | 17:5908260 | GTTGGGAACTGGCAG[A/C]CCTATGGAGGACACG | 66616 |
rs6390943 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Snx9 | GRCm38.p3 | 17:5908259 | TTGGGAACTGGCAGA[C/T]CTATGGAGGACACGT | 66616 |
rs6391020 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Snx9 | GRCm38.p3 | 17:5908217 | GGAGAACTGGCACCC[A/G]CTTACAGCGCCCATC | 66616 |
rs6392051 | snp | A/C | 0.5 | 0 | intron-variant | Snx9 | GRCm38.p3 | 17:5908059 | GGCTGGCTCACATTC[A/C]GAAAGCTGGAGTACA | 66616 |
rs6392087 | snp | A/G | 0.5 | 0 | intron-variant | Snx9 | GRCm38.p3 | 17:5908041 | AAGCTGGAGTACAGA[A/G]GATCTCCCTGGAGAC | 66616 |
rs6393719 | snp | A/C | 0.5 | 0 | intron-variant | Snx9 | GRCm38.p3 | 17:5914368 | GATGGCTAACTGGCC[A/C]CATGGGCAATGCAGG | 66616 |
rs6394314 | snp | C/T | 0.5 | 0 | intron-variant | Snx9 | GRCm38.p3 | 17:5914239 | aggctggagagatgg[C/T]acactggttaggggc | 66616 |
rs13470482 | snp | C/T | 0.375 | 0.216506 | synonymous-codon | Snx9 | Mm_Celera | 17:5927310 | TGGCACCATGTCTTA[C/T]GCTCTGCAAGGTAAG | 66616 |
rs13470484 | snp | A/C | | | utr-variant-3-prime | Snx9 | Mm_Celera | 17:5930623 | GGTTATGTAAACCAG[A/C]ATGGAACACAAGAGA | 66616 |
rs13470486 | snp | C/T | | | synonymous-codon | Snx9 | Mm_Celera | 17:5891839 | CGACCAAGCTTTCCT[C/T]GATTCCCTGACAGCT | 66616 |
rs13470487 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Snx9 | Mm_Celera | 17:5902380 | AACTGGTGATGATGA[C/T]GAATGGGATGAAGAC | 66616 |
rs29499039 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5871783 | ACATTGATACTCAAA[C/T]AGACACATGACTTTT | 66616 |
rs29499877 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Snx9 | Mm_Celera | 17:5896744 | AATGCCTAGCGTCAT[C/T]TCCTTATTTAAACAT | 66616 |
rs29500832 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Snx9 | Mm_Celera | 17:5905095 | TATCCTGTCCTGCAT[A/G]GTTGGTGATGTGTTC | 66616 |
rs29501268 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5896440 | GCTAAGAAACAGAGC[A/G]GGTTACCGAATGCCC | 66616 |
rs29501664 | snp | A/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5860848 | TTCTTTTTTTTTCTT[A/T]ATTGGATATTTTCTT | 66616 |
rs29503613 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5893254 | TGTCAGGTTGCAGCT[C/G]TCTGCTCAGTCCCAG | 66616 |
rs29515684 | snp | C/T | 0.5 | 0 | intron-variant | Snx9 | Mm_Celera | 17:5890633 | GCCTGAGCATTTGCC[C/T]CTCTTGGGTGACAGA | 66616 |
rs29518128 | snp | C/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5870774 | TGGAAATATAGTTTG[C/T]GATGATGAATGTTGA | 66616 |
rs29519748 | snp | A/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5879510 | GTGTATAGGAAGTAG[A/T]CAGTTACACTGGACC | 66616 |
rs29521239 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5912717 | CATCTGGTCTTCCTT[G/T]CTGTAATTCCCCTTT | 66616 |
rs29522684 | snp | A/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5842605 | AAGTTGGGGCCCAGA[A/T]AAATTCATTTTCTCT | 66616 |
rs29534106 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5890344 | CTTACCTATGAGCCT[A/G]AGCTACAGAGGGTTT | 66616 |
rs29535820 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Snx9 | Mm_Celera | 17:5904156 | CATACTTGCTCCTCC[A/G]GTTTCAACCTGTTTC | 66616 |
rs29536419 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Snx9 | Mm_Celera | 17:5903776 | TTTTCCAGAAAGCCT[A/G]GTGTTTAGCACGTGT | 66616 |
rs29537068 | snp | A/G | 0.455 | 0.143091 | intron-variant | Snx9 | Mm_Celera | 17:5887217 | GAAGCTGTCACATGC[A/G]CACCTAGAGAAGTTC | 66616 |
rs29538024 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5871752 | TTATGTGAGTCCTTC[C/T]AGCTGTTTCTGAAAC | 66616 |
rs29539867 | snp | C/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5896722 | TCAGCTAGCAGAAAA[C/T]AGCCTAAATGCCTAG | 66616 |
rs33052280 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Snx9 | Mm_Celera | 17:5927262 | AACTAGTAAAATTAC[C/T]CCCCAAGACAAGCAG | 66616 |
rs33055402 | snp | C/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5870379 | GCCAGTGCAGTGGCA[C/T]ACAGCTAGTTCTAGA | 66616 |
rs33062094 | snp | C/G | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5873170 | AGCACACTGAGCAAG[C/G]CAGGGGAAGCAAGCC | 66616 |
rs33066918 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5918693 | GTCAGCTCAGGGTGG[C/T]GGGGCACAGATGAAG | 66616 |
rs33073924 | snp | C/G | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5906596 | CCGTCTGCTCCTCTT[C/G]TGCACGTCCTCATCG | 66616 |
rs33087960 | snp | A/G | 0.24 | 0.271948 | intron-variant | Snx9 | Mm_Celera | 17:5860496 | CTGGCTTAGCGTGTG[A/G]GTCCCTGGGTCGGTC | 66616 |
rs33088936 | snp | A/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5860498 | GGCTTAGCGTGTGAG[A/T]CCCTGGGTCGGTCTA | 66616 |
rs33096829 | snp | A/G | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5921552 | CTGAAGAGACCCTGC[A/G]GCTGAGCTCAGCAGT | 66616 |
rs33100988 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5886491 | TCGAAAATCAGAGCT[A/G]TTTGGGAGAACTGGC | 66616 |
rs33110228 | snp | A/G | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5896718 | ATCTTCAGCTAGCAG[A/G]AAACAGCCTAAATGC | 66616 |
rs33112827 | snp | C/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5918617 | TTATTTGTCAGTCCA[C/T]GAGAAGCATGCAGTG | 66616 |
rs33128413 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5915147 | AATGCAGCATGAAAA[A/C]CCACAAGCTAAAGAG | 66616 |
rs33144880 | snp | C/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5886563 | GTGTGGAAGAGTGTC[C/T]GTGTCTGCTGTGTGA | 66616 |
rs33162592 | snp | A/G | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5905547 | TCATCCCGTACTTCG[A/G]TTGTTAGTATGTTTT | 66616 |
rs33162617 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5915681 | CACACACACACACAC[A/C]CCTTCTGGTGATGTA | 66616 |
rs33165179 | snp | A/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5860559 | GAATCCAGGCACCTG[A/T]GAGGCTGGTGCAGGA | 66616 |
rs33166605 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5856786 | CTACTTTTTAATGCA[A/T]TCTTCTCTATGGAAT | 66616 |
rs33168487 | snp | A/G | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5923088 | CCTTAATTCCACCAG[A/G]TAAATCTCTGGCTGC | 66616 |
rs33175449 | snp | A/C/G | 0.375 | 0.216506 | intron-variant | Snx9 | GRCm38.p3 | 17:5879524 | GACAGTTACACTGGA[A/C/G]CTGAGGCCGTGTGTA | 66616 |
rs33177009 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Snx9 | Mm_Celera | 17:5858296 | GCAGGGTCAGACAGA[C/T]GACCTGGCCTGAATC | 66616 |
rs33193119 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5857625 | GGCATGTGCCACATA[C/G]CCAGCAGGAGTCCAA | 66616 |
rs33211282 | snp | A/G | 0.5 | 0 | intron-variant | Snx9 | Mm_Celera | 17:5867240 | GCTCAGCAGGGGTTA[A/G]TCAGGTGTAAAGAGG | 66616 |
rs33214552 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5923833 | AAAAGACAGGGGTGA[C/G]AAGAGCCCCAGGTTA | 66616 |
rs33220860 | snp | A/G | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5892748 | ACATAGTTAGACTCT[A/G]TTTCAAAAAATGAAA | 66616 |
rs33225572 | snp | A/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5871648 | TAAACATTTTATTTT[A/T]AAAAAACTACAACAA | 66616 |
rs33225583 | snp | C/T | 0.5 | 0 | downstream-variant-500B | Snx9 | Mm_Celera | 17:5930788 | CTACGTGCGCTGTTG[C/T]CCAGGATGGCCTTTC | 66616 |
rs33243487 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Snx9 | Mm_Celera | 17:5890036 | ACAGAATTTCTAAGC[A/G]AGTCCTAACATAGCA | 66616 |
rs33244818 | snp | A/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5870239 | TTGACGGTGTCTTCC[A/T]AGGGAGTGTTAGGGC | 66616 |
rs33245252 | snp | A/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5879515 | TAGGAAGTAGACAGT[A/T]ACACTGGACCTGAGG | 66616 |
rs33245370 | snp | C/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5857677 | ACCCCTAATTACTTA[C/T]GTCAGAGTATAGTTC | 66616 |
rs33246306 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Snx9 | Mm_Celera | 17:5905454 | CTAGCAGGTAAAGCC[A/G]GAGTTGATGGCACCA | 66616 |
rs33251981 | snp | A/G | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5863118 | GTAACATCCTTCAGG[A/G]TACAGAGTTCACGAC | 66616 |
rs33263145 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5886159 | TGTTAAAATAGTTGG[A/G]ATTGAAGCAGCTCTG | 66616 |
rs33273104 | snp | A/C | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5862931 | AATTCAAATTTGCAT[A/C]AAAACAAATGGTTCT | 66616 |
rs33288587 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Snx9 | GRCm38.p3 | 17:5908154 | TTAGATGTGATGTTG[G/T]CTAGAACTACAGACC | 66616 |
rs33310171 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Snx9, LOC105246186 | Mm_Celera | 17:5849840 | TCCTGAAAGCACACT[A/G]GAACGCGAAGGAAGC | 66616 |
rs33311343 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Snx9 | Mm_Celera | 17:5919619 | AGACACCAAGAAGAG[C/T]GAACAATGGGAGCTG | 66616 |
rs33312671 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Snx9 | Mm_Celera | 17:5859278 | CCGAGGACCATCTCC[A/C]TCATAAAGTGCGTCT | 66616 |
rs33321474 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5909102 | ATGGAGCAGCCAGCA[C/T]CGCTGCTCATTTCTG | 66616 |
rs33346375 | snp | A/G | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5906726 | CAAGGATGCCTGCAC[A/G]TTTGAAGCCTGTGTA | 66616 |
rs33351423 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5896181 | GAGAGGTATGCTTTT[C/T]CTATGCGGTAATGTG | 66616 |
rs33361851 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Snx9 | Mm_Celera | 17:5915201 | GTTTAAGACTGTCAT[C/T]GTAAATTTGTTCCTC | 66616 |
rs33378813 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5870573 | GAGCTGGATATTGGC[C/T]AACAGGTACCCATTT | 66616 |
rs33380542 | snp | A/G | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5870404 | TCTAGAGGAGGAAGA[A/G]GATACAGAGAGCCAT | 66616 |
rs33381897 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Snx9 | Mm_Celera | 17:5916503 | GCTCAGCGGTTAAGA[A/G]CACTGACTGCTCTTC | 66616 |
rs33382331 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Snx9 | Mm_Celera | 17:5905490 | AGTGCAATCTGTAGT[A/G]GTGAGATGATTGCTA | 66616 |
rs33405068 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Snx9 | Mm_Celera | 17:5885806 | CGTGGTTTCTTTGTC[C/G]GTTGTCCTGGGCTGT | 66616 |
rs33413472 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5915785 | GGTAAGGAAGACCCA[C/T]GGGAGGACACATGAT | 66616 |
rs33415810 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5896375 | CAGAAAGTGTTGCTC[A/G]GTGGGCATGACTGGG | 66616 |
rs33440030 | snp | A/G | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5877781 | ATGTTTCTACCAACT[A/G]GGAACCAAACATTCC | 66616 |
rs33458681 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5920876 | GGTCTGTATAGTCCA[C/T]GCTGGCTTCTAACGC | 66616 |
rs33478295 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Snx9 | Mm_Celera | 17:5903383 | GGTTCATGGGCACCT[C/T]AGATCCCCGGGTAGA | 66616 |
rs33480957 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Snx9 | Mm_Celera | 17:5904989 | GTAAGTCTGCTTGTT[C/T]TTGCCTCTTTGTCTT | 66616 |
rs33490396 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Snx9 | Mm_Celera | 17:5855305 | TTTAATCCCAGCACT[C/T]GGGAGGCAGAGGCAG | 66616 |
rs33507566 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5896206 | AATGTGAAGCTCTAC[C/T]GGGCCTGGTCAGGCA | 66616 |
rs33508112 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Snx9 | Mm_Celera | 17:5857034 | GATGGCACCTCTTTA[A/G]GGTCTGTTTTGTATA | 66616 |
rs33519034 | snp | C/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5879595 | ATAGGAAGTAGTCAG[C/T]AGACACTGGAGCTGA | 66616 |
rs33525165 | snp | A/C | 0.5 | 0 | intron-variant | Snx9 | Mm_Celera | 17:5906924 | ATGTGTTCTTAAAGC[A/C]ATAAGGACTTGTGCT | 66616 |
rs33528047 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Snx9 | Mm_Celera | 17:5912981 | AGCTTGTTACTTAAC[C/T]AGGCTGACCTCAGGG | 66616 |
rs33533181 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Snx9 | Mm_Celera | 17:5912865 | AAAGACATTGGAGCC[C/T]CTAATTCTAGGCAAT | 66616 |
rs33535640 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Snx9 | Mm_Celera | 17:5919787 | CACGCCCTCTTACTC[C/T]ATGTGTCCCGTATAG | 66616 |
rs33539922 | snp | A/G | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5842708 | ATAATTGCCTTGTTA[A/G]TAGTATATCTGAGCA | 66616 |
rs33549390 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5900107 | CAAGGAAATGGCAGA[A/G]CATGCCGCCTGGCTC | 66616 |
rs33551658 | snp | A/G | 0.5 | 0 | intron-variant | Snx9 | Mm_Celera | 17:5863618 | TATGTATATATATAT[A/G]TATATATATATATAT | 66616 |
rs33565704 | snp | C/G | 0.46875 | 0.121031 | intron-variant | Snx9 | Mm_Celera | 17:5906831 | CTTGTGAACGTGGCT[C/G]TCTTTGCTAGAAACA | 66616 |
rs33566283 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Snx9 | Mm_Celera | 17:5860069 | CACAAGTACCATTAA[A/T]GTCCGTGTGTCTCCT | 66616 |
rs33596420 | snp | C/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5872510 | AGGCTCCTGCAGTCT[C/T]CGTCCTCCTGTGGTT | 66616 |
rs33598311 | snp | G/T | 0.401235 | 0.199068 | intron-variant | Snx9 | Mm_Celera | 17:5916702 | AACAGGAGCAGCAGT[G/T]CGAGCATGGCTGTTA | 66616 |
rs33598711 | snp | A/G | 0.5 | 0 | intron-variant | Snx9 | Mm_Celera | 17:5862241 | GACTAAGGTATCTGT[A/G]TTGAGGACTGAGCCA | 66616 |
rs33600946 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5855784 | AAGAGAGTCTTAAAG[C/T]CCACAGCCATAGTGG | 66616 |
rs33618804 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5892450 | GAGGGCCTGCGGAGA[A/G]GGAAGGAAGCAGACA | 66616 |
rs33622990 | snp | A/G | 0.5 | 0 | intron-variant | Snx9 | Mm_Celera | 17:5863612 | TATGTATATGTATAT[A/G]TATATGTATATATAT | 66616 |
rs33623261 | snp | A/G | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Snx9, LOC105246186 | Mm_Celera | 17:5845391 | AGGGAAAGTAGAGTC[A/G]GGGAGATCCACATTC | 66616 |
rs33626792 | snp | A/T | 0.304688 | 0.243945 | intron-variant | Snx9 | Mm_Celera | 17:5858201 | AAGCAAAACCAATGC[A/T]ATCTCTATTCTTATT | 66616 |
rs33635975 | snp | C/T | 0.5 | 0 | intron-variant | Snx9 | Mm_Celera | 17:5862178 | TTGAGAATTCTTTGT[C/T]TAGCTCTGTACCTTT | 66616 |
rs33651091 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Snx9 | Mm_Celera | 17:5859309 | GAGACCCAGTAAGGG[C/T]GGGTGTGAAGCCTGC | 66616 |
rs33659350 | snp | G/T | 0.432133 | 0.171253 | intron-variant | Snx9 | Mm_Celera | 17:5903584 | TTGGAGACTCACTGC[G/T]TGTGGATTTGGACAG | 66616 |
rs33672021 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Snx9 | Mm_Celera | 17:5886968 | ACTTAACATTTGTAA[C/T]GTCCTCTTTTCCTGC | 66616 |
rs33679987 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Snx9, LOC105246186 | Mm_Celera | 17:5846848 | AAATACAGCATGCCA[C/T]GTGTGAAATATTCCC | 66616 |
rs33682721 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Snx9 | Mm_Celera | 17:5903994 | TCTTAGGAAGATTGG[C/T]TGTGATGGGCATTGC | 66616 |
rs33684232 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5903887 | AGCTCTCAGACCACA[A/C]ACTCTCCTGCTGCCC | 66616 |
rs33689026 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5844417 | ACATTATATGTATGT[G/T]TTATGCAGCCTTTTG | 66616 |
rs33709929 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Snx9 | Mm_Celera | 17:5859888 | GGCTCTGCGGCAAGG[C/T]GAGCTACGTGAAGTT | 66616 |
rs33714948 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Snx9 | Mm_Celera | 17:5869829 | AGAGGAGGTAGGGAT[C/T]GTGTCCTCTGCAGCA | 66616 |
rs33715545 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5920744 | GGTAGCTCAGGAAAC[A/G]TCATAAAAAACACCA | 66616 |
rs33716483 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5900120 | GAGCATGCCGCCTGG[C/G]TCAGGAGGCTGTGCT | 66616 |
rs33726010 | snp | C/G | 0.33241 | 0.236027 | intron-variant | Snx9 | Mm_Celera | 17:5905053 | GCTAGGAACATTAGT[C/G]CTTTTGGAAGTATTT | 66616 |
rs33726663 | snp | A/G | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5927530 | TTACTTCTAAGTGAC[A/G]CATTCTGTTAACAGC | 66616 |
rs33854505 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5851608 | GGAAGTGTGTATGTG[A/T]GAGAGAGAGAGTTGG | 66616 |
rs33886601 | snp | G/T | 0.5 | 0 | intron-variant | Snx9 | Mm_Celera | 17:5924968 | TGGGTTTTTTTTTTT[G/T]ATTTTTCGAGACAGG | 66616 |
rs33887072 | snp | C/T | 0.5 | 0 | intron-variant | Snx9 | Mm_Celera | 17:5888330 | ATGTCCTCCTAGTTC[C/T]CCCCACAGCCCCTAG | 66616 |
rs45635849 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Snx9 | Mm_Celera | 17:5886003 | TTTTCCACTGAACAT[A/T]ATGAAGCACCCGTTA | 66616 |
rs45641919 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Snx9 | Mm_Celera | 17:5879002 | TAGGGAACACAGAAG[G/T]CGAGATGGAACAGAC | 66616 |
rs45687898 | snp | G/T | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5854667 | AAGACTCGGGATCAA[G/T]TAGGCCTGACAGCAT | 66616 |
rs45688571 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Snx9 | Mm_Celera | 17:5900735 | TGGTATCCTTTTCTC[C/T]CTAATGTCTTTGAAT | 66616 |
rs45714931 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5860449 | CCAACAACTGAGGAC[A/G]CCTGAGCTGGGCTGA | 66616 |
rs45768444 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Snx9 | Mm_Celera | 17:5887748 | TGTTGCTCAGAAGTA[A/C]ACAATACCATTATTA | 66616 |
rs45856827 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Snx9 | Mm_Celera | 17:5893811 | CTGGTCCAGGTGCTC[C/T]AACCATGTAGCTAGG | 66616 |
rs45903466 | snp | A/C/G | 0.231111 | 0.249285 | intron-variant | Snx9 | GRCm38.p3 | 17:5890754 | CCGTTAAAATCGAGC[A/C/G]GTGAGGAGTCTTAAA | 66616 |
rs45913750 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Snx9 | Mm_Celera | 17:5874623 | TCTTTGACAGAACTC[C/T]TGTACTCCCAGAATC | 66616 |
rs45974745 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5873047 | TCAGTTGAGGAAATG[C/T]CTCCATGAGATCCAA | 66616 |
rs45984370 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Snx9 | Mm_Celera | 17:5911518 | ATTTTTTTGAGCTCG[A/G]CATTTGTTTCCAGTT | 66616 |
rs45993697 | snp | A/C | | | intron-variant | Snx9 | Mm_Celera | 17:5896926 | CGACAGCCTCTAAAA[A/C]TTGCTATGTAGCAGG | 66616 |
rs46006134 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Snx9 | Mm_Celera | 17:5912314 | TATGTCTGCCAGGTC[C/T]CTTCTGCGGTGATGA | 66616 |
rs46009393 | snp | C/T | 0.5 | 0 | intron-variant | Snx9 | Mm_Celera | 17:5868560 | AAGCAGCCTTCAGGA[C/T]GGCTCCCAGTGCAGA | 66616 |
rs46028006 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5866485 | TAGTGAGCATGGGAA[C/T]GCAGACACATATGCA | 66616 |
rs46068219 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Snx9 | Mm_Celera | 17:5897338 | GACTGTGTATGTGAG[G/T]GACCACGTAAGATGA | 66616 |
rs46145031 | snp | A/G | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5897872 | ACATGAGTGTACAGC[A/G]CCCATACCTGCCTCT | 66616 |
rs46167428 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Snx9 | GRCm38.p3 | 17:5916729 | GTTAGCTCTAGGCTA[C/G/T]GTATGGTCGGGGGTG | 66616 |
rs46168632 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Snx9 | Mm_Celera | 17:5887902 | TTTGAAATAAAAGTT[A/C]TGAGGAAAATTATCT | 66616 |
rs46192198 | snp | A/G | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5860020 | CATCTTCATGTGAGG[A/G]ACTTACGTGCGCAGT | 66616 |
rs46224813 | snp | G/T | | | intron-variant | Snx9 | Mm_Celera | 17:5872719 | CCTCCCCTGTGGGTG[G/T]ACACACTGCACCGGC | 66616 |
rs46233879 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Snx9 | Mm_Celera | 17:5923126 | GCAGTATGGATAGTG[A/G]CACTAGAACAGTGTA | 66616 |
rs46244069 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Snx9 | Mm_Celera | 17:5907263 | CACCTCTCTAGCCTT[A/G]GTTGCAATTTGAAAC | 66616 |
rs46251457 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Snx9 | Mm_Celera | 17:5890514 | TTCAATGGGACACCC[C/T]AAAGTCCTGCGGGTG | 66616 |
rs46285097 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5878802 | CGGGCATCTTTAGCC[C/T]TACGCTGCAGAGTTG | 66616 |
rs46295886 | snp | A/G | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5872475 | GTATAGCTTAATGTC[A/G]TCAGCAAACTCGTAC | 66616 |
rs46296427 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5868345 | TGCAAATTAGACGTC[A/G]CAGCAATGCATGCGC | 66616 |
rs46306316 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Snx9 | Mm_Celera | 17:5878112 | CTCTCAGGGCTCTAT[C/G]TACTTCCTTCTAGAC | 66616 |
rs46369963 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Snx9 | Mm_Celera | 17:5874932 | AGGTGTAAAAAGACA[A/T]AGTGCTTCTCCTCTA | 66616 |
rs46425697 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5913949 | GGTCACGCTTCACTT[C/G]TTTGCCTCAGATGCT | 66616 |
rs46430720 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Snx9 | Mm_Celera | 17:5897470 | TCTTGCACAGGCAGG[C/T]GTGATGGTTTACGGC | 66616 |
rs46437118 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Snx9 | Mm_Celera | 17:5915076 | ATATGGAATTGGCCT[A/G]ACTTGAACGGCAGAG | 66616 |
rs46492366 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Snx9 | Mm_Celera | 17:5929209 | TTTAAAGCCTTGAGC[A/C]GTCCTGACTGTGTGA | 66616 |
rs46494421 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5895442 | TGACAAGTTTCCTTT[C/T]GTTTGCATCTCTGAA | 66616 |
rs46525844 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5843562 | TTGGGATTGCCTTAG[C/T]GCTTATGGGAAAATG | 66616 |
rs46553029 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5873010 | ACTTGACACAGCTGG[A/G]GTTATCACAGAGAAA | 66616 |
rs46567283 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Snx9 | Mm_Celera | 17:5878523 | TATGTTCAGTTGCTG[C/T]TTGTGTTTTTCTCCA | 66616 |
rs46674223 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Snx9 | Mm_Celera | 17:5902431 | CTCACCTTACTTCAA[A/G]GATTCAGAACCAGCT | 66616 |
rs46683110 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5859078 | TGACTGAGAGAGCCT[C/T]TAGCCTTAGTGCACA | 66616 |
rs46719475 | snp | G/T | 0.5 | 0 | intron-variant | Snx9 | Mm_Celera | 17:5869627 | CCAGGATAATTCCTC[G/T]GTGACCCACGTTCCT | 66616 |
rs46735246 | snp | C/T | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5922707 | TTCTCTTGTGGCTCT[C/T]CATAAAGCATACAGT | 66616 |
rs46739054 | snp | C/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5870935 | TACCAAGCTGGACTT[C/T]GTAATCATGTGGCTC | 66616 |
rs46788732 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5885452 | TCGCTTTGCGTGTCA[C/T]TGTCTCGCATTCCAC | 66616 |
rs46821078 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Snx9 | Mm_Celera | 17:5922200 | GTTCAGCTCCAGCGG[C/T]TATCAAGGTACGGGG | 66616 |
rs46822140 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Snx9 | Mm_Celera | 17:5898998 | TACTGTAGAGCCATT[A/T]GGTCAGTGGTAAGGG | 66616 |
rs46832041 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Snx9 | Mm_Celera | 17:5907783 | CGGCTGATGATGGCT[G/T]TCAGGCTGTGGCCAG | 66616 |
rs46847122 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5905907 | GTCTTCTGAGTAGTT[A/G]AAGAAGAGTTGAATC | 66616 |
rs47005099 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5916054 | ACTTCTCACTTCTTC[C/T]CCAGGCTCTTCTCTG | 66616 |
rs47005516 | snp | A/T | | | intron-variant | Snx9 | Mm_Celera | 17:5879480 | AGTAGACAGTTACAC[A/T]GGAGCTGAGGCCGTG | 66616 |
rs47028837 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5876843 | GTTGTGTTAATTTAC[C/G]ATGTAAAGACTGTGA | 66616 |
rs47035486 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5906253 | GTCGGCTGACAACTA[C/G]TATTACTCACTGATG | 66616 |
rs47104507 | snp | A/G | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5886826 | ATGTGCAGGGGCTCT[A/G]GTCATTGGGTTCTGA | 66616 |
rs47147684 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Snx9 | Mm_Celera | 17:5887123 | CTGTGGATGTGCGTT[A/C]ATGTGGTGCCTTTCT | 66616 |
rs47152244 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Snx9 | Mm_Celera | 17:5887594 | ACGAGCAGCTCTGAC[C/T]ACACCGCTCTTCCCT | 66616 |
rs47171732 | snp | C/T | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5887136 | TTCATGTGGTGCCTT[C/T]CTTCTACATGCTCAG | 66616 |
rs47172410 | snp | C/T | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5887658 | CTGGGTTCAGACTCC[C/T]TCTGGTGGAAATTTA | 66616 |
rs47176116 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5926705 | TGGAGCTGTCTTTGC[A/G]GGGGACATAAGTACT | 66616 |
rs47211704 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Snx9 | Mm_Celera | 17:5918568 | GGTACAGTCACAGGG[A/T]ATTTATGTCTGAAAC | 66616 |
rs47212388 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5898553 | ACTCGGGAAACTCGG[A/G]AAACCCCAGGAACTC | 66616 |
rs47217745 | snp | C/G | | | intron-variant | Snx9 | Mm_Celera | 17:5898570 | AACCCCAGGAACTCT[C/G]AGGAGACAGGGAGAG | 66616 |
rs47242930 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Snx9 | Mm_Celera | 17:5899416 | GGGCTCCAGGACAGA[C/T]GGAACTAGCGCTCAG | 66616 |
rs47260717 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Snx9 | Mm_Celera | 17:5878160 | ATAAATCAGTGTTTA[A/G]AACCCAAACCACAGC | 66616 |
rs47273194 | snp | A/G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5891681 | CTGCAGCCCTGAAGC[A/G/T]TCGGCCCCTCCCCAG | 66616 |
rs47275020 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Snx9 | Mm_Celera | 17:5887513 | CCCAGCAGGGCCACA[A/T]CACCGTGTTCATAAA | 66616 |
rs47338728 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Snx9 | Mm_Celera | 17:5906079 | GCAGAACAGGAAGGC[C/T]AGCCTGTGCGCTGCC | 66616 |
rs47398591 | snp | A/T | | | intron-variant | Snx9 | Mm_Celera | 17:5862636 | TAGAATTCAACCTAA[A/T]TGATGCCTCCTTAAC | 66616 |
rs47422031 | snp | C/T | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5874011 | GATTGAGCTGGGCAG[C/T]CAGTACCTTTGCCTA | 66616 |
rs47468248 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5897424 | GTGTGTGTGACCTGC[G/T]TGCTGCCATCATGTA | 66616 |
rs47496475 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5921629 | GGATGCACGGGTGGC[C/T]TGAGATGAGGGTCTC | 66616 |
rs47518463 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5893030 | GCTTGGTTCTCGATC[A/C]CTTTCTAGTCCAGCT | 66616 |
rs47680842 | snp | G/T | | | intron-variant | Snx9 | Mm_Celera | 17:5899102 | TTTTCCCCTGGGTCA[G/T]GGCATGGAGACTTAA | 66616 |
rs47694740 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Snx9 | Mm_Celera | 17:5917268 | GCTGGCCACTAACTT[C/T]TTCTGACAGCCTCCT | 66616 |
rs47725817 | snp | C/G | 0.297521 | 0.245442 | intron-variant | Snx9 | Mm_Celera | 17:5899118 | GGCATGGAGACTTAA[C/G]TCCATTTCCAGTGAC | 66616 |
rs47751039 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Snx9 | Mm_Celera | 17:5906308 | ACCCAAGCAGTTGCC[A/C]TTTGTCCTCTTCACA | 66616 |
rs47756265 | snp | C/T | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5920003 | AAGTATCCGTGGCTA[C/T]GCAGTGATGCTGAGT | 66616 |
rs47773192 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Snx9 | Mm_Celera | 17:5874688 | TAGCTCCTTCTCTCA[A/G]TTTCAGTAAGGAGTT | 66616 |
rs47778309 | snp | A/G | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5885527 | CCTGGGGAGCAACTG[A/G]ATTTAGCTGAACTGA | 66616 |
rs47807185 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5860686 | GTCATGGAGAGAAGA[C/T]GCTTAATAATAATGC | 66616 |
rs47826731 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5900768 | AAACAGTTTTCATTC[A/G]TTAGTTTGTTTCTTA | 66616 |
rs47829522 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5862345 | GGTGTCTTAATCATC[A/G]CATCTGCTTTTAGGT | 66616 |
rs47834364 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Snx9 | Mm_Celera | 17:5922800 | GCATGTGGGTTTACT[C/T]TTCCTGAGCAGAGTG | 66616 |
rs47859942 | snp | A/G | 0.142012 | 0.225474 | synonymous-codon | Snx9 | Mm_Celera | 17:5920660 | GCAGGAGCACTGGAA[A/G]CGCTGCACAGGGCGT | 66616 |
rs47874247 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5897922 | CGACTTCATTCTCAG[C/G]TCCTTCTGGTGTGAT | 66616 |
rs47881781 | snp | G/T | | | intron-variant | Snx9 | Mm_Celera | 17:5904205 | CTGAAGCAAAAAGGT[G/T]GTCTTTAGTTAAGAG | 66616 |
rs47883787 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5905840 | AGATAGAAGTGTAAC[A/G]TCATCCAAAGCCCTG | 66616 |
rs47992009 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5895617 | CACGTCGGAGGACCC[A/G]CACTTTTGTCTCTCA | 66616 |
rs48009677 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Snx9 | Mm_Celera | 17:5893345 | AGAGGTGGAGCCTTG[C/T]ACGCACAGCAAGCCT | 66616 |
rs48009959 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Snx9 | Mm_Celera | 17:5889261 | TCACACATGACCACA[G/T]TTCCCATGGACACCC | 66616 |
rs48015153 | snp | A/T | | | intron-variant | Snx9 | Mm_Celera | 17:5898225 | GCAGGGAGAGAGAGG[A/T]TTCTGGGCAATAGTG | 66616 |
rs48074255 | snp | A/T | | | intron-variant | Snx9 | Mm_Celera | 17:5898445 | GCAGCCCTGAGGAGG[A/T]GATGGCTATAGAGCA | 66616 |
rs48096336 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5903861 | CTATTTACATAACAC[A/G]GGGCTAAAAGAGCTC | 66616 |
rs48111669 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5924860 | GCTTTGTAGCTTACA[C/T]CTGTAGCTTACACCT | 66616 |
rs48128378 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5923653 | TCTGTCAGAGACGAT[C/T]GAGGCCGCTTCTGGA | 66616 |
rs48148052 | snp | A/C | 0.375 | 0.216506 | intron-variant | Snx9 | Mm_Celera | 17:5891086 | TTTCTAAAGAGGTAT[A/C]GTTTCAGCTTCTTAG | 66616 |
rs48175062 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5897241 | TGGGAAGCAGCCTTG[A/G]CCCCATGGTCACAGA | 66616 |
rs48202037 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Snx9 | Mm_Celera | 17:5929587 | GGTGCTCAGCCTGCC[A/G]TTGCCTCCATGCATT | 66616 |
rs48237411 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Snx9 | Mm_Celera | 17:5888690 | GTCTGAGGTTTGTTC[C/T]CCAGTGTTCTTCCTG | 66616 |
rs48241136 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5901074 | AAGACAGTGATTATT[A/G]CAACTTGAAATTGAC | 66616 |
rs48242629 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5896902 | TGGGACAGGGTCTCC[C/T]TGTGTAGCCGACAGC | 66616 |
rs48262102 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5864310 | AGCATGGGAACCAGA[C/T]ACATAGTGAGCATGG | 66616 |
rs48357166 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5891413 | CAGGGGTGTGTGCTC[G/T]CGTCCATGTGTGTCT | 66616 |
rs48357855 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Snx9 | Mm_Celera | 17:5899032 | AGCAGTAGCCTGCAC[A/G]GTGGCTTTCTAGCTC | 66616 |
rs48381277 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5897104 | GAGGAAGGTAGTGTT[C/T]CAGGTCCCATTTAAC | 66616 |
rs48408445 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5880978 | GTGTATAGGAAGTAG[A/G]CAGTTACACAGGAGC | 66616 |
rs48411806 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Snx9 | GRCm38.p3 | 17:5896519 | TTGATGGCCAAAGGA[G/T]CTTTAAAACAGATCT | 66616 |
rs48434120 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5898504 | AGGGAAGACACTGAC[A/G]AAGAAGCAGGCCAGA | 66616 |
rs48437828 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Snx9 | Mm_Celera | 17:5891716 | GATTGTGTGTCACCT[A/C]CTCAAGCTCTCACTG | 66616 |
rs48488958 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Snx9 | Mm_Celera | 17:5926885 | TGTCATAGCAGCAGA[C/G]AGGACACGTGCCCCT | 66616 |
rs48506199 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5897372 | CGGGGCTGAACAGTC[C/T]CATCGGTGATACATG | 66616 |
rs48547348 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5926630 | TCAGGAGGTTGGCTC[A/G]TCAGAACTTGAGCAG | 66616 |
rs48549446 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5900918 | AGGCAGGGCCAAGTG[A/G]ATCTCTTGTTAGTTC | 66616 |
rs48559488 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5897582 | AAAACCCTCTGCTGT[C/T]ACCCCAGCAGTGGTG | 66616 |
rs48568101 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Snx9 | Mm_Celera | 17:5900207 | TTCACTGATCTAGAA[A/G]GCTATCTGTAACCCC | 66616 |
rs48578066 | snp | A/C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5880952 | GACAGTTACACTGGA[A/C/G]CTGAGGCCGTGTGTA | 66616 |
rs48603893 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5923671 | GGCCGCTTCTGGAAG[C/T]GCAAAAACTAGACTC | 66616 |
rs48606946 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5886893 | CTGGTCAGCCACAGG[C/T]ACTGTCAGGTTCACA | 66616 |
rs48609226 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Snx9 | Mm_Celera | 17:5902172 | GTTTCCAATGTGTCA[C/T]TTGCATTCAAAGAAC | 66616 |
rs48628113 | snp | A/C/T | 0.32 | 0.24 | intron-variant | Snx9 | GRCm38.p3 | 17:5897137 | AGTAGCTAAGAAGGG[A/C/T]GAATTGCTCATATGC | 66616 |
rs48628826 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Snx9 | Mm_Celera | 17:5915240 | CTGGCAGGAAGCCTG[C/T]GATGGATTGGACAAA | 66616 |
rs48630410 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Snx9 | Mm_Celera | 17:5926801 | AGTACAGGACCCAGG[A/G]CCTCTCACAAACAAC | 66616 |
rs48632126 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5929050 | AGGGTCTCATGCCCT[C/T]TTCTGACCTCTGCGG | 66616 |
rs48632803 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Snx9 | Mm_Celera | 17:5877909 | GATTCACAGTCTGGA[A/G]GTCCTGGGCCGAGGC | 66616 |
rs48666131 | snp | C/T | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5887544 | CCCTCTTTGAACTTG[C/T]GTGTGCACATAGAGG | 66616 |
rs48702032 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Snx9 | Mm_Celera | 17:5856082 | GCTCCCTGCTCCATG[C/G]TGCCTGAAGTTGTTT | 66616 |
rs48706293 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Snx9 | Mm_Celera | 17:5875459 | TTGCAGCTCAGCCTA[G/T]TGTGCACAGAGCCCG | 66616 |
rs48755794 | snp | A/T | | | intron-variant | Snx9 | Mm_Celera | 17:5843528 | GGAAATGAATGCATC[A/T]CGTGGACAGCTGGTA | 66616 |
rs48764113 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5923360 | CCTGGCCAAGGAAGA[A/T]AATTGGACCATTGGT | 66616 |
rs48797436 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5898148 | TCTTAAAAATATTAC[C/T]TGTCAATAAAAAAAG | 66616 |
rs48800864 | snp | A/C | | | intron-variant | Snx9 | Mm_Celera | 17:5899075 | GACCAGTGCTCACAT[A/C]GTATGCCCCTGTTTT | 66616 |
rs48807426 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Snx9 | Mm_Celera | 17:5904857 | ATTTTAATGAAGACG[A/G]ACAGAGACTCACAGA | 66616 |
rs48837376 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5899956 | AAACCCGACTACATC[A/T]GCAGCCCTTCTCCAG | 66616 |
rs48841423 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5891257 | TCTGAACTATAAAAC[A/G]CACAATGTGTTTAAA | 66616 |
rs48867837 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5862637 | AGAATTCAACCTAAT[C/T]GATGCCTCCTTAACT | 66616 |
rs48897855 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5904715 | TGTCCCTCTGCCCGT[C/G]CTCAAGCTCCACTGA | 66616 |
rs48930153 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Snx9 | Mm_Celera | 17:5898283 | TGCTGAGGAAGGAGG[C/T]CGGGACTGCAGGAGA | 66616 |
rs48946352 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5905114 | GGTGATGTGTTCTTA[G/T]GAGCACTACGGATAA | 66616 |
rs48956051 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Snx9 | Mm_Celera | 17:5913992 | TTTCCCAAATAAACC[A/G]CATCTGCTCTTTGTA | 66616 |
rs48967123 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5856157 | TCAGCTTACCTGAAT[A/G]TGGAAGCATCCATGT | 66616 |
rs48987074 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Snx9 | Mm_Celera | 17:5887333 | ATCTGTTGTGGTTCT[C/G]AAATCAACTCCCAGT | 66616 |
rs48987517 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Snx9 | Mm_Celera | 17:5901461 | CTTCAGGAAGGAAAC[C/T]CTGAGTAAGGAGGCC | 66616 |
rs48990240 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Snx9 | Mm_Celera | 17:5908783 | AGTGTGAGTGGTGAC[A/G]ACTGACGCTGTGAAG | 66616 |
rs48995411 | snp | C/T | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5920468 | AATCTCTTTTGTGCT[C/T]GTCCTTGGAATCAAA | 66616 |
rs49008062 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Snx9 | Mm_Celera | 17:5858266 | TACTCCAGCACCATG[C/G]TAAATGCCCAAGCGG | 66616 |
rs49017039 | snp | C/G | | | intron-variant | Snx9 | Mm_Celera | 17:5843798 | AATCCTGTTCCTCTG[C/G]AAGAGCAGTGGTGCT | 66616 |
rs49032043 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5862063 | GCCATTCTGACTGGT[A/G]TGAGGTGGAATCTCA | 66616 |
rs49038893 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Snx9 | Mm_Celera | 17:5899425 | GACAGACGGAACTAG[C/T]GCTCAGAGGAACAGC | 66616 |
rs49061890 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5929565 | AGTGAGCGCTTGCGG[G/T]AGCCTTGGTGCTCAG | 66616 |
rs49131458 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5879085 | AGAGCTGTGCACTCA[A/G]CAGCACATGTGTTGT | 66616 |
rs49211240 | snp | G/T | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5921724 | CCCATAGCTGAGGCT[G/T]CATATACCCTCCTCT | 66616 |
rs49225705 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5890293 | GCTAATTAAATAAAG[C/T]GCGGGAAATACATTG | 66616 |
rs49233237 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Snx9 | Mm_Celera | 17:5898088 | ATATATTCCTCTGCA[C/T]CTTAGGAGGCTTTGA | 66616 |
rs49264361 | snp | C/G | | | intron-variant | Snx9 | Mm_Celera | 17:5895976 | ATTAAAAGCTTTGCT[C/G]TGCCTTGTCCCCTGC | 66616 |
rs49328581 | snp | A/G/T | 0.32 | 0.24 | intron-variant | Snx9 | GRCm38.p3 | 17:5877999 | ACGGAACCACTCACC[A/G/T]CTGCAAACAAGAGGA | 66616 |
rs49384461 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5919278 | AGCCAGTGCCCATCG[C/T]TTCCCTGCCTCCCGG | 66616 |
rs49423656 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5879176 | GGCCCTAGATTGATG[C/T]CCACCAGCCATACCT | 66616 |
rs49423790 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Snx9 | Mm_Celera | 17:5857298 | GAGCACTAATTCAGT[G/T]GCATAGCTCCAATGG | 66616 |
rs49439193 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5916590 | TGGGATCTGATGCCC[C/T]CTTCTGGTGTGTGTG | 66616 |
rs49462401 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Snx9 | Mm_Celera | 17:5899861 | GACTGACCGTGGTCG[C/T]TACCACCACCAGCGT | 66616 |
rs49483256 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5893055 | CCAGCTACTAAATGT[C/T]TACCCAATGCCTGAT | 66616 |
rs49536474 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Snx9 | Mm_Celera | 17:5887455 | TGTTCTTAGCCTGAC[C/T]CTGTAGTAGGATTAC | 66616 |
rs49612952 | snp | A/C | | | intron-variant | Snx9 | Mm_Celera | 17:5898233 | AGAGAGGTTTCTGGG[A/C]AATAGTGAGAAGCAG | 66616 |
rs49618276 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Snx9 | Mm_Celera | 17:5906136 | GAATCTGTGGGCAGG[C/T]GTGGGCAGGCCACTG | 66616 |
rs49623104 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Snx9 | Mm_Celera | 17:5885807 | GTGGTTTCTTTGTCC[G/T]TTGTCCTGGGCTGTG | 66616 |
rs49708097 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Snx9 | Mm_Celera | 17:5858895 | AGTGCTGGTACTCAG[A/G]GTGAGAGAAGGCAGT | 66616 |
rs49709425 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5881032 | GACAGTTACACTGGA[G/T]CTGAGGCCGTGTGTA | 66616 |
rs49727640 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Snx9 | Mm_Celera | 17:5886708 | GTGGACCCATTACCA[A/G]TGCCTGCATCTGCTT | 66616 |
rs49745489 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5859463 | TAGAGACCCGCTCGG[A/G]CGGCTTCTGGCTTTG | 66616 |
rs49803968 | snp | A/C | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5918629 | CCACGAGAAGCATGC[A/C]GTGCAGTGAGAAGAG | 66616 |
rs49829800 | snp | A/C | | | intron-variant | Snx9 | Mm_Celera | 17:5860431 | ATAAGGGGCAGGGGA[A/C]AGCCAACAACTGAGG | 66616 |
rs49830637 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5902090 | ACTGATTGAAGGAAG[A/G]TACAGTCTGTTGTGT | 66616 |
rs49851958 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Snx9 | Mm_Celera | 17:5860780 | TAAACAGGCTTCTCT[C/G]AGTTAGAAATCTCTG | 66616 |
rs49926881 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5890174 | ACCCACGACCAGCTA[C/T]GCTCATCTTCGCTGC | 66616 |
rs50045435 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Snx9 | Mm_Celera | 17:5910918 | TGTCTCATTGTACAT[C/T]ATTCCAGCAGTCCTA | 66616 |
rs50053740 | snp | A/C | | | intron-variant | Snx9 | Mm_Celera | 17:5898742 | GAGAATCTTGGATTT[A/C]TTTTTTATACAGATA | 66616 |
rs50067882 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Snx9 | Mm_Celera | 17:5879019 | GAGATGGAACAGACG[C/T]GAGCAGTGTGGGCGA | 66616 |
rs50074328 | snp | A/G/T | 0.142012 | 0.225474 | intron-variant | Snx9 | GRCm38.p3 | 17:5904820 | TAAAACTGGTGTGGT[A/G/T]AGGTCACATGGTGAG | 66616 |
rs50084499 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Snx9 | Mm_Celera | 17:5897690 | TTGTGGCCCTAGGCA[A/G]TAGGCCATAGCATTT | 66616 |
rs50088251 | snp | A/G/T | 0.165289 | 0.235211 | intron-variant | Snx9 | GRCm38.p3 | 17:5921988 | AAGAAATCAGTAGTT[A/G/T]AAAAATCATTTCATC | 66616 |
rs50120531 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5862397 | CCTTTGAGCGACTTT[C/T]ATTCTTAGGTTATAT | 66616 |
rs50149106 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Snx9 | Mm_Celera | 17:5885335 | GCTCAGAACACCGGA[C/T]CCGGGGTGATGGCTG | 66616 |
rs50158755 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5890636 | TGAGCATTTGCCTCT[C/T]TTGGGTGACAGACAC | 66616 |
rs50200110 | snp | A/G | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5926241 | CCTACGTGTATCCAC[A/G]AGAAATGTGGTGGTG | 66616 |
rs50204762 | snp | C/G | | | intron-variant | Snx9 | Mm_Celera | 17:5862742 | ATTTATTTATTATAT[C/G]TAAGTATACTGTGGC | 66616 |
rs50326273 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Snx9 | Mm_Celera | 17:5912426 | ACTGCCATTTCAGTC[A/G]CACACTGTTGGTAGA | 66616 |
rs50361303 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5872689 | CCAGAGCGTACGCTT[C/T]CTTTACTGTGCTGTC | 66616 |
rs50364261 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Snx9 | Mm_Celera | 17:5892951 | CCTTTTGAGAGAAAC[A/G]GTTAAATCTCCATCA | 66616 |
rs50397347 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5897453 | TAAAAGAGCGCGTTC[A/G]GTCTTGCACAGGCAG | 66616 |
rs50403675 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5891189 | TGGTTGAACCATCAG[A/G]ACCATTCACCAACAG | 66616 |
rs50406465 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5875893 | CACCTGTTAGTGCCT[C/G]TGCCCTTTGACTAGG | 66616 |
rs50408029 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5902323 | TCACTCAGAGTTAAG[C/T]TTCTCACATGCGTGG | 66616 |
rs50422901 | snp | C/T | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5894141 | ACATCTTAGTCCCTG[C/T]GTGAACATGAGAAGT | 66616 |
rs50438235 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Snx9 | Mm_Celera | 17:5909688 | GAGGGCAGTGGACTG[A/T]GTGGGAGAGTCAGGC | 66616 |
rs50494855 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Snx9 | Mm_Celera | 17:5907800 | CAGGCTGTGGCCAGT[C/T]TCACACTGCTCCAAG | 66616 |
rs50495471 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5862416 | CTTAGGTTATATTCG[C/T]GGCACTCTCTTTGCT | 66616 |
rs50504326 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5898258 | AAGCAGGAGAGACCC[A/G]AGAGCCATTTGCTGA | 66616 |
rs50543200 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Snx9 | Mm_Celera | 17:5897505 | TGCTGGTTTGTTGTT[C/T]ACTACTCTTCACAGC | 66616 |
rs50607941 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5897857 | CCTGTGGTTATAGAT[A/G]CATGAGTGTACAGCA | 66616 |
rs50664717 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Snx9 | Mm_Celera | 17:5860270 | AGAGGGGAGAGCAGA[C/T]GTCACAGGTTGTCCT | 66616 |
rs50665412 | snp | A/G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5872702 | TTTCTTTACTGTGCT[A/G/T]TCCTCCCCTGTGGGT | 66616 |
rs50694610 | snp | A/T | | | intron-variant | Snx9 | Mm_Celera | 17:5898732 | AGGCTGGAAAGAGAA[A/T]CTTGGATTTCTTTTT | 66616 |
rs50747943 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Snx9 | Mm_Celera | 17:5874873 | GGTAATAGCTGTGAC[A/G]TTTGCTTTGCCTGGA | 66616 |
rs50768456 | snp | G/T | | | intron-variant | Snx9 | Mm_Celera | 17:5916592 | GGATCTGATGCCCCC[G/T]TCTGGTGTGTGTGAA | 66616 |
rs50784011 | snp | C/T | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5877977 | TTCACAGTAGGACTG[C/T]GTGCTGACGGAACCA | 66616 |
rs50803983 | snp | G/T | | | intron-variant | Snx9 | Mm_Celera | 17:5900747 | CTCCCTAATGTCTTT[G/T]AATTAAAACAGTTTT | 66616 |
rs50826914 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5887106 | CGGGCGAGCGTACAG[C/T]GCTGTGGATGTGCGT | 66616 |
rs50839391 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5930203 | GCACATAGCAGATTC[C/T]CAGTGCACCCTGGGC | 66616 |
rs50934868 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Snx9 | Mm_Celera | 17:5906386 | CTGCGGCAGCTTAAT[C/T]GTGTATTCTTGGAGA | 66616 |
rs51035013 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Snx9 | Mm_Celera | 17:5902204 | GGGCAGGATTCATAG[C/G]TCAAGCCTTAATGCC | 66616 |
rs51045049 | snp | A/T | 0.5 | 0 | intron-variant | Snx9 | Mm_Celera | 17:5878568 | GCCTGTTTTCCTGTT[A/T]GGCTGCTATTTCTTG | 66616 |
rs51056880 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5900396 | ACTGCGTGCACATGG[C/T]ACACAGAAACCCAGA | 66616 |
rs51077288 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Snx9 | Mm_Celera | 17:5920750 | TCAGGAAACGTCATA[A/C]AAAACACCATAGTAG | 66616 |
rs51084311 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Snx9 | Mm_Celera | 17:5878823 | TGCAGAGTTGCTTAT[A/G]GCTTGTTTTGTATTA | 66616 |
rs51092553 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5922099 | CACTTCAGACCGCTC[C/T]GAGAACTAATCAGTT | 66616 |
rs51105881 | snp | C/G | | | intron-variant | Snx9 | Mm_Celera | 17:5875046 | TTCCTCATTCAAGTC[C/G]CAGGCACATGCTGTT | 66616 |
rs51119246 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Snx9 | Mm_Celera | 17:5885759 | AAGCAGAATTCTATC[A/G]ACTGTGCAGCTGTGT | 66616 |
rs51132043 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Snx9 | Mm_Celera | 17:5875364 | GCAGCCCTGGGGGTT[A/C]AGAAGAGTAGTGAGA | 66616 |
rs51158053 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Snx9 | Mm_Celera | 17:5921106 | CAGTAGATGTGTCAG[A/G]CAGACTAGGCCACTA | 66616 |
rs51199100 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Snx9 | GRCm38.p3 | 17:5885180 | CAAATTCAAGACTCT[A/G]TTAGCCCTCCTTCTG | 66616 |
rs51228819 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5865169 | GCATGGGAACCAGAC[A/G]CATAGTGAGCATGGG | 66616 |
rs51252293 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5893411 | GTGGCTAGGGAGGTT[C/T]CCTGGTGGACTTACC | 66616 |
rs51268232 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Snx9 | Mm_Celera | 17:5877682 | TGTCTACTCATGAGA[C/T]CTTTTCCTGGGTTGC | 66616 |
rs51297524 | snp | C/T | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5904354 | CATTAAAGCCTTATG[C/T]AGTATCTTGAAGTAG | 66616 |
rs51302164 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5898224 | AGCAGGGAGAGAGAG[A/G]TTTCTGGGCAATAGT | 66616 |
rs51329545 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5843775 | AGTCACGTGGATTCT[A/G]GGAACCAAATCCTGT | 66616 |
rs51348511 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5872983 | GTTCATGTACTGGCT[A/G]GTTTTGTGTCAACTT | 66616 |
rs51429676 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5887779 | AATCATCCAGGCCAC[A/G]CACGCTCTGTTATCT | 66616 |
rs51431637 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5885551 | GAACTGAAAAATGCA[A/G]CAGGCATCTCAAGGA | 66616 |
rs51506674 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Snx9 | Mm_Celera | 17:5858383 | TCCTCCTCACAGGGC[A/G]TGTTTTACCCGAGCA | 66616 |
rs51523794 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Snx9 | Mm_Celera | 17:5895847 | GTGTTAGTGCTTCAG[C/T]CGTGGTACCAAGCAC | 66616 |
rs51531476 | snp | G/T | | | intron-variant | Snx9 | Mm_Celera | 17:5873117 | GCCCCTTGTGGGTGG[G/T]ACCATCTCTGGGCTG | 66616 |
rs51555273 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Snx9 | Mm_Celera | 17:5887411 | TCATGCCGACGGTCC[C/T]AAACAGCTTAGTTTC | 66616 |
rs51569769 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Snx9 | Mm_Celera | 17:5902224 | GCCTTAATGCCGACT[A/G]CAAAGCCTGTGCTCT | 66616 |
rs51570872 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5900546 | CACAAACCGCACCCC[A/G]CCCCGCCCGAGAAGG | 66616 |
rs51629421 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5865657 | GAGCATGGGAACCAG[A/C]CACATAGTGAGCATG | 66616 |
rs51672896 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5907016 | GTGTAGCTGACATAG[C/T]GCCTTGGACCCCTCA | 66616 |
rs51684143 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5893927 | CATGAGTTCAATTCC[C/T]AGCAACCACATGGTG | 66616 |
rs51705621 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5899135 | CCATTTCCAGTGACT[A/G]TACCAGCACTTATGT | 66616 |
rs51723443 | snp | G/T | | | intron-variant | Snx9 | Mm_Celera | 17:5891185 | AATATGGTTGAACCA[G/T]CAGAACCATTCACCA | 66616 |
rs51828524 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Snx9 | Mm_Celera | 17:5923972 | GAGCCATGACCTTTT[C/T]CTAGGTGTGCCGCAG | 66616 |
rs51851378 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Snx9 | Mm_Celera | 17:5893630 | AGAAAGTCATGGAAG[C/T]CAAAGCCCTTCTTCT | 66616 |
rs51881320 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5872685 | AGTGCCAGAGCGTAC[A/G]CTTTCTTTACTGTGC | 66616 |
rs51915210 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Snx9 | Mm_Celera | 17:5907309 | TGGGATAGCAGAGAT[A/G]GTCAGAGGTCAAGAC | 66616 |
rs51922178 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Snx9 | Mm_Celera | 17:5925605 | TGCCTGCCCTCTCTA[A/G]CTTGCTTTCCTCATC | 66616 |
rs52004219 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Snx9 | Mm_Celera | 17:5897269 | AGAACAGTTCAAAAG[C/T]CACCTAGGTGGCCAG | 66616 |
rs52021702 | snp | C/G | | | intron-variant | Snx9 | Mm_Celera | 17:5862415 | TCTTAGGTTATATTC[C/G]CGGCACTCTCTTTGC | 66616 |
rs52034022 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5899078 | CAGTGCTCACATCGT[A/G]TGCCCCTGTTTTCCC | 66616 |
rs52039112 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5878958 | TCCTTAAGTGAGACA[C/T]GAGTGATTTTTCAGT | 66616 |
rs52064014 | snp | G/T | | | intron-variant | Snx9 | Mm_Celera | 17:5896380 | AGTGTTGCTCGGTGG[G/T]CATGACTGGGGAGGG | 66616 |
rs52079506 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5918169 | GCGCACACACACACA[C/T]ACACACACACACACA | 66616 |
rs52222245 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Snx9 | Mm_Celera | 17:5901448 | ATAGAGAATGAAACT[A/T]CAGGAAGGAAACTCT | 66616 |
rs52239246 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Snx9 | Mm_Celera | 17:5875987 | ACCCTGTCCTGAAAA[C/T]CCACCAAATAAAGGT | 66616 |
rs52293609 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Snx9 | Mm_Celera | 17:5876058 | AGAGTTGCAGGAACC[A/G]TTTAACCGCGTGATA | 66616 |
rs52316471 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Snx9 | Mm_Celera | 17:5917233 | TTAATTTCTAGGTAC[A/G]GTTTGCCTGTGTAAC | 66616 |
rs52323352 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5906982 | GTATTTTTGCTTTTA[C/T]TTTTGAGACAGGGTC | 66616 |
rs52367775 | snp | A/C | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5886206 | GAGTTCAGGCTGGTC[A/C]TTCTCTGCTGGCTGC | 66616 |
rs52384803 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5906904 | AAAGTCCATTTTGTA[A/G]GACAATGTGTTCTTA | 66616 |
rs52393976 | snp | C/T | 0.32 | 0.24 | intron-variant | Snx9 | Mm_Celera | 17:5874372 | ATTGCCTCACTTTGG[C/T]ATACACACACACACA | 66616 |
rs52396649 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5918171 | GCACACACACACATA[C/T]ACACACACACACACA | 66616 |
rs52508334 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5901270 | AGCTGCACTGTTTAC[C/T]TTCCCATCCACATCC | 66616 |
rs107625073 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5928740 | ATCCCCCCATGTACA[C/T]GTGTGAAGGGAGGGA | 66616 |
rs107697632 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5930361 | CCCCACCACCAGGCA[C/T]GGCCTGGCCTTGGAC | 66616 |
rs107772279 | snp | G/T | | | intron-variant | Snx9 | Mm_Celera | 17:5929947 | AAGGTGCTCATACTG[G/T]GGATTTATTAATTAT | 66616 |
rs107793920 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5930165 | TGAGCCTAAGGGTAT[C/T]GAGTACCCTTATGGG | 66616 |
rs107827273 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5929758 | TACATTTAAACAGGT[A/G]CATTTAAAACACATG | 66616 |
rs107855971 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5930553 | GAAATGTCTCAACTG[C/T]TCTGTTTTTTCACCA | 66616 |
rs107886006 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5855724 | GAGAGTTATACATCT[C/T]GTTCTGAAGGCAAAC | 66616 |
rs107920161 | snp | C/G | | | intron-variant | Snx9 | Mm_Celera | 17:5928357 | CCCAACACCCCCCAT[C/G]CACAGGTGTGTCCCC | 66616 |
rs107942222 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5927872 | TTAGTTAGAAAGAAA[A/G]CAGCTGATTTCTAGA | 66616 |
rs108041191 | snp | C/T | | | utr-variant-3-prime | Snx9 | Mm_Celera | 17:5930630 | TAAACCAGAATGGAA[C/T]ACAAGAGAACTCCGA | 66616 |
rs108094681 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5928760 | GAAGGGAGGGAGGTT[C/T]TGGCCTAGTGCCCTT | 66616 |
rs108107848 | snp | G/T | | | intron-variant | Snx9 | Mm_Celera | 17:5928694 | CATCCCCCATCCACA[G/T]GTGTGAGGGCAGTGA | 66616 |
rs108197891 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5883588 | GTAGACAGTTACACA[A/G]GAGCTGAGGCCGTGT | 66616 |
rs108212366 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5930460 | GAGCCTAACAGACCA[A/G]CTAAAGGGTTTGATA | 66616 |
rs108238139 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5883627 | AGTAGACAGTTACAC[A/T]GGAGCTGAGGCCGTG | 66616 |
rs108269925 | snp | A/G | | | synonymous-codon | Snx9 | Mm_Celera | 17:5930617 | CTTCCCGGTTATGTA[A/G]ACCAGAATGGAACAC | 66616 |
rs108301771 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5929864 | GTCGCTGCTGGGCTT[A/G]GCCCCTCTGTGTGTT | 66616 |
rs108336350 | snp | G/T | | | intron-variant | Snx9 | Mm_Celera | 17:5928362 | CACCCCCCATCCACA[G/T]GTGTGTCCCCTCCCA | 66616 |
rs108425160 | snp | C/T | | | downstream-variant-500B | Snx9 | GRCm38.p3 | 17:5931148 | AGGGAAATAGAGTCC[C/T]CAGATCACCTACACC | 66616 |
rs108483774 | snp | G/T | | | intron-variant | Snx9 | Mm_Celera | 17:5929755 | ATGTACATTTAAACA[G/T]GTGCATTTAAAACAC | 66616 |
rs108524518 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5928317 | TGTCCCCTCCCAACA[C/T]CCCCCATCCACAGGT | 66616 |
rs108574960 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5929790 | ACCTGATGTGTGGGG[A/G]TGGACTCACTCTGGA | 66616 |
rs108619893 | snp | C/G | | | intron-variant | Snx9 | Mm_Celera | 17:5841758 | CGGAGACGGGCGCCC[C/G]GGCACGCGGAGTTCC | 66616 |
rs108634270 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5930113 | TACTGTACACTTGCA[C/T]TTCAAATGTTTAAGG | 66616 |
rs108635389 | snp | A/G | | | missense | Snx9 | Mm_Celera | 17:5930597 | CTGAGGCAGGCCCTC[A/G]GCCGCTTCCCGGTTA | 66616 |
rs108635863 | snp | C/G | | | intron-variant | Snx9 | Mm_Celera | 17:5928689 | CCCAACATCCCCCAT[C/G]CACAGGTGTGAGGGC | 66616 |
rs108670110 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5891631 | AAAACTATTGAAATT[A/G]TAGAGTGCAGCAAAA | 66616 |
rs108682983 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5928915 | ATTGGATCAAAAAAG[C/T]TTTCCTGGGCCTGGA | 66616 |
rs108697517 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5929970 | TTAATTATCAAGCCC[A/G]CACATGCTATAATTT | 66616 |
rs108728003 | snp | C/G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5891624 | ATAAATGAAAACTAT[C/G/T]GAAATTGTAGAGTGC | 66616 |
rs108835392 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5928862 | GAGTTTAGTGGTTTG[A/G]TTTTTTTTTTAATCT | 66616 |
rs108849706 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5930254 | TGCCCGCTACCTCCA[C/T]AACAGGGAGTCTTAG | 66616 |
rs108850466 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5882888 | ATAGGAAGTAGTCAG[C/T]AGACACTGGAGCTGA | 66616 |
rs108871545 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5852694 | AAAATTTAAAAAAAA[A/G]AAAAAAAAAAAAAAG | 66616 |
rs108913817 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5928337 | CATCCACAGGTGTGT[C/T]CCCTCCCAACACCCC | 66616 |
rs108917929 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5929637 | TCAGAACACATCTCT[A/G]CATGTGTCGCTTTTG | 66616 |
rs211732965 | in-del | -/C | | | intron-variant | Snx9 | Mm_Celera | 17:5928044 | TGCTGCAGGGGTCAG[-/C]CTGTGTTTCTAGGCT | 66616 |
rs211914288 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5928736 | CAACATCCCCCCATG[C/T]ACATGTGTGAAGGGA | 66616 |
rs213069439 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5929254 | AGCCTCTCCACGCAC[A/G]GGGACAGTGCCAGAG | 66616 |
rs213181195 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5865382 | ATAGTGAGCATGGGA[A/C]CGCAGACACATAGTG | 66616 |
rs213259995 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5930406 | AGACAGGAGCAGGGG[C/T]ACTGAGTCAAACGGC | 66616 |
rs214207582 | in-del | -/TT | | | intron-variant | Snx9 | Mm_Celera | 17:5928862 | AGTTTAGTGGTTTGA[-/TT]TTTTTTTTTTAATCT | 66616 |
rs214892812 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5929482 | TGTGCTGTTCTCCTT[C/T]GTTACACACTTCCAC | 66616 |
rs216328942 | snp | A/T | | | intron-variant | Snx9 | Mm_Celera | 17:5930304 | AAGAAGGGGACTCTG[A/T]GCACTTGCTTTCCGG | 66616 |
rs216649696 | snp | G/T | | | intron-variant | Snx9 | Mm_Celera | 17:5929561 | GAGCAGTGAGCGCTT[G/T]CGGTAGCCTTGGTGC | 66616 |
rs216674483 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5883823 | ATAGGAAGTAGTCAG[C/T]AGACACTGGAGCTGA | 66616 |
rs217036146 | snp | G/T | | | intron-variant | Snx9 | Mm_Celera | 17:5928574 | ACACCCCCATCCACA[G/T]GTGTGAGGGCAGTGA | 66616 |
rs220322069 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5864636 | GGGGACGCAAACACA[A/T]AGAGAGCATGGGAAC | 66616 |
rs221037341 | in-del | -/AG | | | intron-variant | Snx9 | Mm_Celera | 17:5930390 | CCTGACTGGGCAGGT[-/AG]AGACAGGAGCAGGGG | 66616 |
rs221857590 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5928125 | AGTCCTGCTGATGAC[A/G]AGTCTTAGGCAAGCA | 66616 |
rs221958986 | snp | A/T | | | intron-variant | Snx9 | Mm_Celera | 17:5928818 | CTTTACTCCTGAGTG[A/T]TAAACCAAAGGGGCT | 66616 |
rs222655994 | snp | A/G | | | downstream-variant-500B | Snx9 | Mm_Celera | 17:5930942 | ATTTATATATTACCT[A/G]TGATCTTCCAGTTCT | 66616 |
rs223102815 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5864630 | AAACATGGGGACGCA[A/G]ACACAAAGAGAGCAT | 66616 |
rs223336604 | in-del | -/AG | | | downstream-variant-500B | Snx9 | GRCm38.p3 | 17:5931141 | CCGGGATAGGGAAAT[-/AG]AGTCCTCAGATCACC | 66616 |
rs223501909 | snp | A/G | | | downstream-variant-500B | Snx9 | Mm_Celera | 17:5930725 | GAGAGAAAAGGAAGA[A/G]AACCAAAAAGAAAGA | 66616 |
rs227215215 | in-del | -/C | | | utr-variant-3-prime | Snx9 | Mm_Celera | 17:5930684 | GCGATTCAATTCCCT[-/C]CCCCTCCCCGCCCCC | 66616 |
rs227829433 | snp | A/G | | | downstream-variant-500B | Snx9 | GRCm38.p3 | 17:5931069 | AGTCCTTTGGGGATC[A/G]TTGTCTGTTTGGGGG | 66616 |
rs229052701 | snp | C/G | | | intron-variant | Snx9 | Mm_Celera | 17:5928325 | CCCAACACCCCCCAT[C/G]CACAGGTGTGTCCCC | 66616 |
rs230287390 | snp | A/C | | | intron-variant | Snx9 | Mm_Celera | 17:5930140 | AAGGTCCCCAGATGA[A/C]TAAGGAACCTGAGCC | 66616 |
rs230542235 | snp | G/T | | | intron-variant | Snx9 | Mm_Celera | 17:5929306 | CCACAAGTTGTATCG[G/T]TTTCAGTTAGAGAAA | 66616 |
rs230618463 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5865433 | AGTGAGCATGGGAAC[A/G]CAGACACATAGTGAG | 66616 |
rs231698178 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5929064 | TCTTCTGACCTCTGC[A/G]GGCACCAACCACACA | 66616 |
rs232240507 | snp | A/C | | | intron-variant | Snx9 | Mm_Celera | 17:5928550 | GAGGGCAGTGAGTGT[A/C]CCCTCCCAACACCCC | 66616 |
rs232550022 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5929483 | GTGCTGTTCTCCTTC[A/G]TTACACACTTCCACA | 66616 |
rs232583482 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5928786 | CCCTTGACTAGATAG[A/G]CTTGGTCAGTTATAA | 66616 |
rs233812557 | in-del | -/GTCA | | | intron-variant | Snx9 | Mm_Celera | 17:5929848 | TCTTCTGACTTTCCT[-/GTCA]GTCGCTGCTGGGCTT | 66616 |
rs234856320 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5930345 | AGTCTGAAAATGTAG[C/T]CCCCACCACCAGGCA | 66616 |
rs236651103 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5928681 | TGTCCCCTCCCAACA[C/T]CCCCCATCCACAGGT | 66616 |
rs237588462 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5930105 | TGAGTATCTACTGTA[C/T]ACTTGCACTTCAAAT | 66616 |
rs237716954 | in-del | -/A | | | intron-variant | Snx9 | Mm_Celera | 17:5928143 | CTTAGGCAAGCAGAG[-/A]AATGTCATGTTGTTA | 66616 |
rs241365023 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5929139 | AGAAAATGAATAGGT[A/G]TAATCTTTGGAAATG | 66616 |
rs241419462 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5928825 | CCTGAGTGATAAACC[A/G]AAGGGGCTTACATTT | 66616 |
rs241460095 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5928178 | AAGTCTTGCTGGGAA[C/T]TAATCCCTGTGATAA | 66616 |
rs243298943 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5928912 | AATATTGGATCAAAA[A/G]AGCTTTCCTGGGCCT | 66616 |
rs243776749 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5929229 | TGACTGTGTGACTTC[C/T]TTCTTTCTGAGCCTC | 66616 |
rs244404132 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5864639 | GACGCAAACACAAAG[A/T]GAGCATGGGAACGCA | 66616 |
rs244456402 | snp | C/T | | | downstream-variant-500B | Snx9 | Mm_Celera | 17:5931009 | TAAAAATATGAAAAA[C/T]GGCAGAATAAAAAGT | 66616 |
rs245848327 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5929732 | TACACACAAGGTACA[C/T]GTGTTACATGTACAT | 66616 |
rs247570524 | snp | C/G | | | intron-variant | Snx9 | Mm_Celera | 17:5928569 | TCCCAACACCCCCAT[C/G]CACAGGTGTGAGGGC | 66616 |
rs250450372 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5929351 | CGTTGCTTGTGACCC[A/G]GGTTTTACAGTTACC | 66616 |
rs251684423 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5929548 | GGGCAGCACAGAGGA[A/G]CAGTGAGCGCTTGCG | 66616 |
rs251898454 | snp | G/T | | | intron-variant | Snx9 | Mm_Celera | 17:5928813 | ATAATCTTTACTCCT[G/T]AGTGATAAACCAAAG | 66616 |
rs252510989 | snp | A/T | | | missense | Snx9 | Mm_Celera | 17:5899351 | GGCAATGACCCCTGG[A/T]CAGCCTGGAATGCTC | 66616 |
rs253118831 | in-del | -/AG | | | intron-variant | Snx9 | Mm_Celera | 17:5930222 | GCACCCTGGGCTGTC[-/AG]AGATGCAAACTCCAC | 66616 |
rs253290014 | in-del | -/T | | | intron-variant | Snx9 | Mm_Celera | 17:5929048 | AGGGGTCTCATGCCC[-/T]TCTTCTGACCTCTGC | 66616 |
rs253830271 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5928836 | AACCAAAGGGGCTTA[C/T]ATTTTGAACAGAGTT | 66616 |
rs254040645 | snp | A/G | | | missense | Snx9 | Mm_Celera | 17:5928234 | TTTCACAGTAACCGG[A/G]TCTATGATTACAACA | 66616 |
rs255277378 | in-del | -/CATTTAAACAGGTG | | | intron-variant | Snx9 | Mm_Celera | 17:5929745 | CACGTGTTACATGTA[-/CATTTAAACAGGTG]CATTTAAAACACATG | 66616 |
rs255337799 | snp | A/T | | | intron-variant | Snx9 | Mm_Celera | 17:5928443 | CCATCCACAGGTGTG[A/T]CCCCTCCCAACATCC | 66616 |
rs255866731 | in-del | -/CCTC | | | intron-variant | Snx9 | Mm_Celera | 17:5929445 | AAGGAAAACATAAAT[-/CCTC]CCTCCCTCCCTTCCT | 66616 |
rs256645691 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5930154 | ACTAAGGAACCTGAG[C/T]CTAAGGGTATTGAGT | 66616 |
rs258753474 | snp | A/T | | | downstream-variant-500B | Snx9 | GRCm38.p3 | 17:5931169 | CACCTACACCCTCAA[A/T]CTTGGTGGTGGGTAG | 66616 |
rs259886200 | in-del | -/CC | | | intron-variant | Snx9 | Mm_Celera | 17:5928381 | GTCCCCTCCCAACAT[-/CC]CCCCATGCACATGTG | 66616 |
rs260727110 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5929898 | CATAGTAGGTTACAT[A/G]TGTCTCTGAGAAAAC | 66616 |
rs260887565 | snp | C/T | | | utr-variant-5-prime | Snx9 | GRCm38.p3 | 17:5841435 | GCGCCGGGCCGCAGC[C/T]ACCGAACCGCAGACG | 66616 |
rs260915306 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5929197 | TTGGTTCCTAGTTTT[A/G]AAGCCTTGAGCAGTC | 66616 |
rs261890935 | snp | A/G | | | intron-variant | Snx9 | Mm_Celera | 17:5928747 | CATGTACATGTGTGA[A/G]GGGAGGGAGGTTTTG | 66616 |
rs262143322 | snp | C/T | | | downstream-variant-500B | Snx9 | Mm_Celera | 17:5930790 | ACGTGCGCTGTTGCC[C/T]AGGATGGCCTTTCTT | 66616 |
rs262834683 | snp | C/T | | | intron-variant | Snx9 | Mm_Celera | 17:5928487 | TGTCCCCTCCCAACA[C/T]CCCCATCCACAGGTG | 66616 |
rs265587653 | snp | A/G | | | downstream-variant-500B | Snx9 | Mm_Celera | 17:5931023 | ACGGCAGAATAAAAA[A/G]TATATCTTTGTATAT | 66616 |
rs387204379 | in-del | -/T | | | intron-variant | Snx9 | Mm_Celera | 17:5914747 | ACTGTTTCTGTTGAC[-/T]TTTTTTTTTCTCCTT | 66616 |
rs387725721 | in-del | -/C | | | intron-variant | Snx9 | Mm_Celera | 17:5928045 | GCTGCAGGGGTCAGC[-/C]TGTGTTTCTAGGCTC | 66616 |
rs578268356 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5897803 | AGAAACTAGGTTATT[A/G]GACACCATGTTGCCT | 66616 |
rs578268992 | snp | C/T | | | synonymous-codon | Snx9 | GRCm38.p3 | 17:5899392 | GAACTGGGACAGCTC[C/T]GATGCCTGGGGCTCC | 66616 |
rs578337846 | snp | A/T | | | intron-variant, upstream-variant-2KB | Snx9, LOC105246186 | GRCm38.p3 | 17:5848554 | CCTTCTCCCTCAAAC[A/T]TTTTAGCTCCACCTT | 66616 |
rs578342003 | snp | C/T | | | intron-variant, downstream-variant-500B | Snx9, LOC105246186 | GRCm38.p3 | 17:5845275 | GTTTTTGCTATCTCT[C/T]GCCTTTATCACCTGA | 66616 |
rs578351304 | snp | A/T | | | upstream-variant-2KB | Snx9 | GRCm38.p3 | 17:5840343 | CACACAAACATCCAC[A/T]GAAAACTCTGAATTA | 66616 |
rs578356064 | snp | A/G | | | intron-variant, upstream-variant-2KB | Snx9, LOC105246186 | GRCm38.p3 | 17:5850203 | AGTCTGCCTGGCTGG[A/G]CTCTCAAATTTTATG | 66616 |
rs578363667 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5852076 | ATCTGAAACGAGCCT[C/T]GTTAGCGTGCTGCAG | 66616 |
rs578366341 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5843292 | CCTCGTTAAAGGGAA[C/T]TCCTCTGCGCTTTTC | 66616 |
rs578370211 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5856628 | TCCTTGAGTCCAGTT[G/T]ATACTCCCTCCAAAC | 66616 |
rs578374773 | snp | A/G | | | intron-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5847214 | ACCACAAAATCCCCT[A/G]TGTCTCTTTCCACTG | 66616 |
rs578384422 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5924086 | AGCTGGTCACTGTCT[C/G]AGTTAGAGTTTCTAT | 66616 |
rs578385513 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5927599 | GAGCTGGTGGGATGG[C/T]TCAGTGGTTAAGAAC | 66616 |
rs578387794 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5918120 | AGATGTGGGCACGCA[C/T]GTGTGTGCGCACACA | 66616 |
rs578389251 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5925930 | AGGCCAGCCAGACCC[G/T]AAACAGTGAGAGCAT | 66616 |
rs578391069 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5860376 | TCTTAGCCTGCACAC[C/G]TGCACAGCAGCACAT | 66616 |
rs578394056 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5919354 | ACTGTGTTCTTCACT[A/G]TACCCCTATTCTCCA | 66616 |
rs578394310 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5853989 | TCAAGACTTTCTCCC[G/T]TGGAATACACCTTCC | 66616 |
rs578396751 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5862358 | TCGCATCTGCTTTTA[C/G]GTGTGCTTAAATCCT | 66616 |
rs578397842 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5921159 | TTAGGTTACCCATGG[C/T]TCTGCTCACCTCCCT | 66616 |
rs578398719 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5871094 | TACTATAATCACAAA[G/T]CCATATATATGATTT | 66616 |
rs578406488 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5868148 | AAACTGTTTCTATGG[C/T]GAGAGATATCTGCTA | 66616 |
rs578407567 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5915012 | CTAAGTACCTGTTTT[C/T]GCAGCTCTGGATGCT | 66616 |
rs578414561 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5922100 | ACTTCAGACCGCTCC[A/G]AGAACTAATCAGTTA | 66616 |
rs578442583 | snp | A/G | | | intron-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5848058 | TAACCCAGTAAATCA[A/G]AACTCTAGAAGCTTA | 66616 |
rs578454831 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5844090 | AGGCCTTGAGAGTGT[C/T]TCAGTCTTGACCTGT | 66616 |
rs578464180 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5857370 | CACTGGCTCTTTGCA[C/T]GCATGTGATTCACTG | 66616 |
rs578468578 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5923231 | AGTAAGACAGCCAGC[C/T]GTGAGAAGGCGTAAG | 66616 |
rs578469294 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5851206 | AGAGATGGCAGTGTG[A/T]GTGCCTGAGAGAGAT | 66616 |
rs578472242 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5854442 | TCATCCACTCAGACC[C/T]TGATATCCCAGTCCG | 66616 |
rs578477036 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5926781 | CTGCTTCCATCCAGA[A/G]TGAGAGTACAGGACC | 66616 |
rs578477606 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5863292 | ACCTGAGTGTGGAAG[C/G]CCAGGAGCCATGTGA | 66616 |
rs578482721 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5859693 | TCAGAGGGCAGCTTT[G/T]GGGAGTTGGTTCTCT | 66616 |
rs578483568 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5921668 | TCAGAGTGCTCCTCA[A/G]ATCCAAACCTGGACC | 66616 |
rs578487451 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5925067 | TCCGACTGCCTCTGC[C/T]TCCCAAGTGCTGGGA | 66616 |
rs578491317 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5918794 | ACTTGCTGCACAAAC[A/C]TGAGGCCCTGAGTTC | 66616 |
rs578495929 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5871983 | AGTGAATCCTTGGGA[C/T]GCACCTGTCCCCACC | 66616 |
rs578501663 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5915459 | GAAACTTAGGGTTTT[C/T]TTTGGGCAGATGATG | 66616 |
rs578502319 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5867558 | TAGTAACGTTCAGAC[A/C]TAGCTTATGTAGTGT | 66616 |
rs578507434 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5877704 | CTGGGTTGCTACACC[A/G]TGTACTATGGTGGTA | 66616 |
rs578509273 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5913122 | ATAGATCATTTGGTT[C/T]GCATCGTACTTAGGA | 66616 |
rs578512749 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5870692 | CCCGCACTTGGCTTT[C/T]GCTTTTAAAAGAAGA | 66616 |
rs578514767 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5868883 | ACCCAGGGAAGGCTC[C/T]GAGCCCCACCCTGGG | 66616 |
rs578516595 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5860971 | CACCCACTCCTGCTT[C/T]CTGGCCCTGGCATTT | 66616 |
rs578523850 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5907052 | CTGTCTTCACTTTCC[A/G]TGTTCTAGGATTACA | 66616 |
rs578525169 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5873286 | AACAGCAGGGTGGAA[A/G]TGTAAGCCGAATAAA | 66616 |
rs578527570 | snp | C/G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5888187 | CTATGTCCTCCTAGT[C/G/T]CCCCCCACAGCCCCT | 66616 |
rs578529099 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5879403 | GACAGTTACACTGGA[A/G]CTGAGGCCGTGTGTA | 66616 |
rs578531301 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5876413 | TGTCCCAATTTCATC[C/T]CCTCCTCTTACTACT | 66616 |
rs578533101 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5861855 | TTCTTACCAGTTGGA[G/T]CATCTTCTGGGTCTA | 66616 |
rs578533342 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5892063 | GGTGTGTGCAGTGTG[A/G]GGGTGTGTACAGTGG | 66616 |
rs578535047 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5874626 | TTGACAGAACTCTTG[C/T]ACTCCCAGAATCCTT | 66616 |
rs578535581 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5887095 | CCCGGTAAGAGCGGG[C/T]GAGCGTACAGTGCTG | 66616 |
rs578538099 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5900679 | TGCTCACTGCCCTTC[C/T]CCCACGTCTGTCTCC | 66616 |
rs578541660 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5894470 | TAGCTAGCTACCCTC[A/G]TCCAGTTTTTAGAGT | 66616 |
rs578547826 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5890339 | AAGAGCTTACCTATG[A/G]GCCTAAGCTACAGAG | 66616 |
rs578547945 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5905202 | TTAATGTTGAACCGT[C/T]ACTCATACATTTCAG | 66616 |
rs578549083 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5885077 | TTTGTGAGTCTGCAT[C/T]CATTTGTGCTGCCAC | 66616 |
rs578550227 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5893448 | GTAATCTGTATTAAT[G/T]GGGCTGGCCTTTGAG | 66616 |
rs578552028 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5902346 | ATGCGTGGTTGTTCT[C/T]GTTCTCCCTCCCTAT | 66616 |
rs578557062 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5856794 | TAATGCAATCTTCTC[G/T]ATGGAATCCCAACAA | 66616 |
rs578558362 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5855052 | GGTCCAGTGGGCCGT[C/T]ACAGGCCGCACAGTA | 66616 |
rs578559362 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5903395 | CCTTAGATCCCCGGG[A/T]AGAATGTGGCATTCC | 66616 |
rs578565205 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5858297 | CAGGGTCAGACAGAC[C/G]ACCTGGCCTGAATCC | 66616 |
rs578566462 | snp | C/T | | | intron-variant, upstream-variant-2KB | Snx9, LOC105246186 | GRCm38.p3 | 17:5848659 | CTCTGGAGGCAGAGG[C/T]AGGCGGATTTCTGAG | 66616 |
rs578569050 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5866866 | CCAGACACATAGTGA[G/T]CATGGGAACCAGACA | 66616 |
rs578569149 | snp | C/G | | | intron-variant, upstream-variant-2KB | Snx9, LOC105246186 | GRCm38.p3 | 17:5850300 | TGCCCTGGCCTATTC[C/G]AGATTCCCCAGTGAC | 66616 |
rs578571101 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5854124 | CGATCTGAAGGAGGG[A/G]GTGGTCCTGGCTGCG | 66616 |
rs578573369 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5861354 | GCATCCACAACAGTG[C/T]TTGGGTTTGGTGATT | 66616 |
rs578578873 | snp | A/G | | | utr-variant-3-prime | Snx9 | GRCm38.p3 | 17:5930672 | TACCTGGGGCAATGC[A/G]ATTCAATTCCCTCCC | 66616 |
rs578579648 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5869383 | ATTCTATTCTGCCTT[C/T]GCTGTGGAAAAGGCT | 66616 |
rs578580449 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5926676 | AGGCCTGGAGCCTCG[C/T]TTACACTTCACAGTG | 66616 |
rs578583658 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5875348 | TGAACTTGTATTCCT[A/G]GCAGCCCTGGGGGTT | 66616 |
rs578584798 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5921728 | TAGCTGAGGCTTCAT[A/G]TACCCTCCTCTTGAG | 66616 |
rs578589360 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5852322 | GAAGGTCTTGACATG[C/T]GGGGTGCCTACAGTT | 66616 |
rs578590168 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5915573 | TGATACTAAGAAGGA[C/T]CCAGTAGACTTTGGA | 66616 |
rs578591058 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5922925 | GGCATTAAATGTACT[A/C]AGTATATTTTATGAC | 66616 |
rs578593744 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5925263 | CGGATTTCTGAGTTC[A/G]AGGCCAGCCTGGTCT | 66616 |
rs578594931 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5860393 | GCACAGCAGCACATG[C/T]TTCCTGTCCCCGCTC | 66616 |
rs578597910 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5872770 | GCCATAGCCTAGGTC[A/G]GCTCAGCTTGTTTCC | 66616 |
rs578598346 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5868162 | GTGAGAGATATCTGC[C/T]ACAGTGAGGCCATGG | 66616 |
rs578601361 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5920027 | GCTGAGTGTGCTAGG[C/T]GTCGGCCTGTGGTGC | 66616 |
rs578606915 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5914591 | ACTCTAGAACTTCCA[A/T]TCTGTAATTCTGCCT | 66616 |
rs578607467 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5874367 | ATGAGATTGCCTCAC[C/T]TTGGTATACACACAC | 66616 |
rs578607651 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5909914 | CACCCTGTCTCCGGG[A/G]GCCAGCACTCTGTGT | 66616 |
rs578608154 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5878653 | TTCTAATTTTGATTA[A/T]TTGATTTGGGAAGGT | 66616 |
rs578610898 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5907213 | AGTTGCTGTGAGCCC[A/G]AGTGTTAGCCTGGGG | 66616 |
rs578610913 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5916759 | GATTGCCTTTGCCAT[G/T]TAACCTAAGACAAAG | 66616 |
rs578613185 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5911066 | GTGCGCCACCATGCC[C/T]GGCTGAAAATTTTAG | 66616 |
rs578614494 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5918901 | CTGACTACCGTCCTA[C/G]CTCCAGGGTCAGTGA | 66616 |
rs578617339 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5903610 | GACAGTCCGCTGAGG[A/G]ATCTGGGGGCTGGGG | 66616 |
rs578618528 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5913276 | AGGCATGTGGTGGCG[C/T]TCTGTCTCTGTTGCC | 66616 |
rs578619753 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5889083 | AATAGGTTTAGTTTT[C/T]AGACAGAATGACAAT | 66616 |
rs578623948 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5883192 | CACAGGAGCTGAGGC[C/T]GTGTGTATAGGAAGT | 66616 |
rs578624902 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5862535 | GTGTGGCTGCTGTTT[G/T]TTTTCCCACTTGACT | 66616 |
rs578625568 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5908508 | CTCAGAACGAAGCTG[G/T]CTGCTGCTGGCCCTT | 66616 |
rs578630254 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5905268 | CTTACAGCACATTCA[C/T]GTTCTGTTTCCATGC | 66616 |
rs578631154 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5871320 | AGTCTCACTGTATGG[C/T]CCTGGCTGGCTTGGA | 66616 |
rs578633644 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5887783 | ATCCAGGCCACGCAC[A/G]CTCTGTTATCTCTGT | 66616 |
rs578635093 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5891164 | GACCCAGCAGGCTAA[C/T]GTTAGAATATGGTTG | 66616 |
rs578636162 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5876954 | TGGCTAGGTTTATAG[G/T]ATCAGACACGCCTAT | 66616 |
rs578637765 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5885596 | GCAGGTTGCTCCCCA[G/T]CCTGGAGCTGGGCCA | 66616 |
rs578641585 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5894006 | GAAGACAGCTACAGT[C/G]TACTCACATAAAATA | 66616 |
rs578642218 | snp | A/G | | | missense | Snx9 | GRCm38.p3 | 17:5899423 | AGGACAGACGGAACT[A/G]GCGCTCAGAGGAACA | 66616 |
rs578648020 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5898799 | GAGCAGTGCTGAAAT[G/T]TAGTTGGGGTTAGGT | 66616 |
rs578648826 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5892465 | AGGAAGGAAGCAGAC[A/C]CTGAGGTGGCCAGTT | 66616 |
rs578656868 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5902553 | ATGCAGGGACCTGTG[C/T]GTGCGTGCGTGCGTG | 66616 |
rs578698734 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5872142 | TTGACCTGTGGTTCA[C/T]CTTCATTTAAGGCTT | 66616 |
rs578701715 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5876156 | GTTCTCTCTCTCTCT[A/C]TCTCTCTCTCTCTCT | 66616 |
rs578702633 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5879224 | ATTTCTGTTGAGGTG[A/G]TTGATTGTGGTTGAC | 66616 |
rs578704849 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5868906 | ACCCTGGGATAGGTG[G/T]CGAGGAAGGCCTGCC | 66616 |
rs578708791 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5874790 | TGGCTGACCCCACCC[A/T]GTTGGGTGGAGGTCT | 66616 |
rs578710489 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5916257 | CTAGCGAGCGAGCAT[A/G]GTCGTCTCTCCCTCT | 66616 |
rs578711622 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5913875 | AAGTTTGATAGTTGG[A/G]TTCTGCATGCGTGTC | 66616 |
rs578714936 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5886564 | TGTGGAAGAGTGTCC[A/G]TGTCTGCTGTGTGAG | 66616 |
rs578718046 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5885189 | GACTCTATTAGCCCT[C/T]CTTCTGTGCATCAGG | 66616 |
rs578719267 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5910496 | TATTTATTTATTCAT[G/T]TATTTATTTATTTAT | 66616 |
rs578721775 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5907747 | ATTACAGGTGTGTAC[C/T]ACCACACCCAACACA | 66616 |
rs578722593 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5877823 | CTGTGCGGCCCATCC[A/T]CGGCCAGACCAGCAT | 66616 |
rs578728911 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5904517 | CGTAATAATAATTAC[C/T]GTTCATAGATGTGAA | 66616 |
rs578731839 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5892086 | TACAGTGGTTGGGGG[C/G]ATGGGGTGTGGCGTG | 66616 |
rs578738255 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5901420 | CCTGCTGTGTCTCAG[A/G]CCATGGTTACCCATA | 66616 |
rs578750639 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5888581 | GTTCCCCCCACAGCC[C/T]CTAGGCTCCACACCA | 66616 |
rs578760944 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5894616 | CTCCATCTGCATAGT[G/T]TCCATGCCTATGGTC | 66616 |
rs578825323 | snp | A/G | | | upstream-variant-2KB | Snx9 | GRCm38.p3 | 17:5840499 | GAAGCTACAAATTTG[A/G]CAGTAAAATTAAATA | 66616 |
rs578839467 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5894058 | AACTATAAACTGAGA[A/G]CTCCTCACTGTGTAG | 66616 |
rs578858191 | snp | A/G | | | intron-variant, downstream-variant-500B | Snx9, LOC105246186 | GRCm38.p3 | 17:5845344 | GTAGCTTTCAACACA[A/G]TTTAGTGATGTCCAC | 66616 |
rs578882844 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5898838 | AGGCATAATCCGTGA[A/G]TTACAGACCAAGGAC | 66616 |
rs578921230 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5844410 | GTATCTGACATTATA[C/T]GTATGTTTTATGCAG | 66616 |
rs578937044 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5841788 | CCGTAGCCCCGGAGC[A/T]GCGCGCGGGCCACTC | 66616 |
rs578939582 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5861764 | GTATCCATTCCTCTG[C/T]TGAGGGACATCTGGG | 66616 |
rs578942438 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5854592 | CAGGCAGGTTGCCCT[G/T]TCATCCTGACCTCAC | 66616 |
rs578945388 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5855774 | GGCAGCTTGGAAGAG[A/G]GTCTTAAAGTCCACA | 66616 |
rs578949577 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5851413 | GTGTGAGAGAGATGG[C/T]TGTGTGTGTGTGAGA | 66616 |
rs578951895 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5920184 | AGAAATGTAAGAGTC[A/G]CTCCCTGGCATCCTT | 66616 |
rs578952005 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5870468 | ATGATCTTTAAAAAA[C/T]AGTGGTAACTGTAGT | 66616 |
rs578957831 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5924727 | ATTGGTTGTTTAAAC[C/T]CAAACAGCTGTCCCC | 66616 |
rs578960094 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5864013 | CCAGCAAGACACGCA[A/G]ACACCTACGTAAGCG | 66616 |
rs578966498 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5857463 | TTGTGGCTTATAACG[C/T]GTAGAGCACACCTTG | 66616 |
rs578967281 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5853050 | TCTGTCTGTCTCTCT[C/G]TCTCTCTTTCTCTCT | 66616 |
rs578968625 | snp | C/T | | | intron-variant, upstream-variant-2KB | Snx9, LOC105246186 | GRCm38.p3 | 17:5849201 | TTAAGATCTGATTCG[C/T]TACTCATTGTTTTCA | 66616 |
rs578970469 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5861002 | CCCTACATGGGCATA[A/G]AGCCTTCATAGGAGC | 66616 |
rs578971329 | snp | C/T | | | intron-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5848130 | CACAAGCTGCCCACA[C/T]AATAATTTCAGAGCC | 66616 |
rs578972708 | snp | C/T | | | intron-variant, nc-transcript-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5846384 | GGGATGGAAATCTCA[C/T]CCTGCCCCACCCGCA | 66616 |
rs578977734 | snp | A/C | | | upstream-variant-2KB | Snx9 | GRCm38.p3 | 17:5839477 | CTTTGCTGACGTGTC[A/C]CAGTCTGAATGGAGA | 66616 |
rs578981065 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5926740 | GGTGTCTGGAGCTGC[A/G]TGAGGACCAGCGCCA | 66616 |
rs579000239 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5859453 | GGTGTCTAGTTAGAG[A/C]CCCGCTCGGGCGGCT | 66616 |
rs579004754 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5923173 | CCCTGCCAAACCATG[A/T]AACATCCCATAGTCT | 66616 |
rs579007598 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5867399 | ATCCTGGCCATAGAC[A/G]TCTGCTGAGTAGAGT | 66616 |
rs579010683 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5916864 | CCAGCACTCAGATGG[C/T]GGCTCACAATTGCCT | 66616 |
rs579012515 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5873178 | GAGCAAGGCAGGGGA[A/G]GCAAGCCAGTAAGTA | 66616 |
rs579017096 | snp | A/G | | | intron-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5847105 | GATCTCTGTGAGTTT[A/G]AGGCCAGCCTAGTCT | 66616 |
rs579027565 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5852530 | TGCAAAGAGAGGCCC[A/C]TTGGACTTGCAAACT | 66616 |
rs579041305 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5843048 | TCCAGTGAAAAAGCA[C/T]GGCTGTCCTTGGGCT | 66616 |
rs579051115 | snp | A/G | | | intron-variant, downstream-variant-500B | Snx9, LOC105246186 | GRCm38.p3 | 17:5845588 | GGTGGCTGCCTCCTT[A/G]AGGATGCTGTGGGTC | 66616 |
rs579052406 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5853928 | CACACAGACATATAT[A/G]CGTGCAAAACACCAA | 66616 |
rs579052847 | snp | C/T | | | intron-variant, upstream-variant-2KB | Snx9, LOC105246186 | GRCm38.p3 | 17:5849906 | CTTTGGGGATGTTTG[C/T]GTGAGCATTTGGATG | 66616 |
rs579054036 | snp | A/G | | | upstream-variant-2KB | Snx9 | GRCm38.p3 | 17:5840695 | TACAGATCCAACTGC[A/G]GACAAACTACTCTCA | 66616 |
rs579056765 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5858314 | CCTGGCCTGAATCCT[C/T]TCCATGCTTGCTGCT | 66616 |
rs579064470 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5860265 | GTGGTAGAGGGGAGA[A/G]CAGACGTCACAGGTT | 66616 |
rs579067776 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5923815 | CACTCCTAACACCCC[A/C]CAAAAAGACAGGGGT | 66616 |
rs579067947 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5866892 | AGACACATAGTGAGC[A/G]TGGGAACGCAGACAC | 66616 |
rs579069993 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5917884 | ACATGGCACAAGGAC[C/T]TGAGCTCAGATCTCC | 66616 |
rs579072417 | snp | A/G | | | intron-variant, upstream-variant-2KB | Snx9, LOC105246186 | GRCm38.p3 | 17:5848761 | AAACAAGTTAAGGTG[A/G]GGAGAAGGTTCTTAA | 66616 |
rs579077153 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5872871 | ATTCCTTTTTGAGTG[A/G]AAATTTTTAAAAGCA | 66616 |
rs579077407 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5855060 | GGGCCGTTACAGGCC[A/G]CACAGTAGCCATCGT | 66616 |
rs579081006 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5856535 | TCTCTCAACAAAGTA[A/G]AGATCAGGGAAGACG | 66616 |
rs579082588 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5868083 | TTAGTTCTGTTCCAG[G/T]GCTGAGAAGATGGAG | 66616 |
rs579082756 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5922241 | TACTTTTCTTGTTAG[G/T]AACTGTACAGTGATT | 66616 |
rs579084693 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5927332 | CAAGGTAAGAGAAAG[A/G]GTGGTGAGTAACTGG | 66616 |
rs579085404 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5878695 | GGTGTATGTGTGGAA[G/T]TCAAAGGGTAACGTG | 66616 |
rs579088262 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5861432 | CCTCAGTCTCTACTC[C/T]ACACTTCGTCTCTGT | 66616 |
rs579089467 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5911912 | GCATCAGCTCTGTGC[A/G]CAGACTACCTCACTG | 66616 |
rs579090350 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5862317 | AGGCAGGAGGGCTGA[A/G]TACCTGCATCCTGGT | 66616 |
rs579090513 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5926171 | CACAAGGTAAGTCAC[C/T]GTGCTCTCAGGGCCT | 66616 |
rs579092404 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5919456 | GTAGCAGCAAGTGCT[A/G]CATACAGTATGACCC | 66616 |
rs579094662 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5875418 | GAGAGTGGCCTGGGA[C/T]TAAGTAAGAAGCCAG | 66616 |
rs579096235 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5871034 | ATAATAATAATACCA[A/G]TAATACTTACGCTTT | 66616 |
rs579096941 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5901533 | GTTGGGGGTGGGTTG[C/T]TCTTTTGGAGATTTT | 66616 |
rs579098389 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5906410 | TTGGAGACCTCTTTA[A/G]TGCCATGTTACTGGT | 66616 |
rs579104593 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5920975 | GCTCGGGACTGCTTC[C/T]TGTCTTTATGTGCCT | 66616 |
rs579104998 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5885686 | ATCTCCCCCTGCCCT[C/T]GCCGCAGAGGGCTGA | 66616 |
rs579105708 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5914131 | GCCTCATGCCCACAG[A/G]AGCCAGAAAAGGGCT | 66616 |
rs579106804 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5869472 | TATGTTGTTGGCAGG[G/T]AGCCACAGCAAAGCT | 66616 |
rs579109348 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5889389 | CAATGGGAAGACAGG[C/T]CCTTTGGGAAAGCAC | 66616 |
rs579109835 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5916562 | CCACATGGTGGCTCA[C/T]AACCATCTGTAATGG | 66616 |
rs579114254 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5892644 | GCCTAGCGTGAGCCC[C/G]TGTTTTAGAGAATGT | 66616 |
rs579114285 | snp | A/G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5902929 | ACAGCTGCACACAGC[A/G/T]GCACACAGCAGCACA | 66616 |
rs579117367 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5910552 | AGCTGTCTTCAGACA[C/T]CCCAGAAGAGGGCAT | 66616 |
rs579119469 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5895415 | CCGTGATTATCTTTT[A/C]TGTGCCTTGACTGAC | 66616 |
rs579120562 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5907935 | CACTGACAAGTCTTG[A/T]TATGTAAATTTTTAT | 66616 |
rs579120888 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5900136 | TCAGGAGGCTGTGCT[C/T]ATGACTCCTGGCTCT | 66616 |
rs579121637 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5860920 | CCAGAAAACACCCTC[C/T]CCTTATACCCTCCCT | 66616 |
rs579127732 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5914865 | TTTGAGACAGGGTTA[C/T]TTTGTATAGCCCTGG | 66616 |
rs579131082 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5854394 | CAGTCATGGCTGTGC[A/G]CGCCGATCAGTGGGC | 66616 |
rs579131895 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5904673 | CTAAGCAGGTGGAGG[A/G]CCTGTGCGCCACACC | 66616 |
rs579133112 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5927388 | TCAAACCTGCTTGCT[G/T]GTAGAAATCCAAATG | 66616 |
rs579137415 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5909423 | AAAAGACAAAACTAT[C/T]TCTTACAAATGAACA | 66616 |
rs579157063 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5921002 | GCCTGTTCTAGGATG[G/T]GAGAGGCTTTGGTGA | 66616 |
rs579161978 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5857083 | TTGCCTACAGCTTCC[A/G]TTTTAGTTTGTTGTA | 66616 |
rs579162857 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5873275 | CTTTGGTGATGAACA[G/T]CAGGGTGGAAGTGTA | 66616 |
rs579163503 | snp | C/T | | | intron-variant, upstream-variant-2KB | Snx9, LOC105246186 | GRCm38.p3 | 17:5849331 | CTTAGTTCTGATCCT[C/T]ATACTAAAATTGTGT | 66616 |
rs579163660 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5853095 | CTCTCTCTTCTCTCA[A/G]TATTCTCACAGGTGG | 66616 |
rs579168843 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5914909 | TGCTCTGTAGACCAA[A/G]CCAGCCTTGAACTCA | 66616 |
rs579172768 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5918064 | AGGCACAGAGTGATG[A/G]AACAAGATGCTCAGC | 66616 |
rs579173918 | snp | C/T | | | intron-variant, nc-transcript-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5846466 | CTCTAGGGACAAGAC[C/T]CTTGCCGGGCTGGTT | 66616 |
rs579177702 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5859509 | CTTTGCCTCTTGTTT[A/G]CTTGCTTGAAAGACC | 66616 |
rs579183564 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5916056 | TTCTCACTTCTTCCC[C/T]AGGCTCTTCTCTGTC | 66616 |
rs579185027 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5912115 | TTACAAGTCTCTGGA[A/G]CCTGGTTTAAAAACC | 66616 |
rs579185608 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5879296 | GGAACTTTGTGGAAA[C/T]TTAGCTCCATGATGT | 66616 |
rs579185770 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5861846 | CATGTGTCCTTCTTA[C/T]CAGTTGGATCATCTT | 66616 |
rs579186689 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5923948 | GCTGCTCTGCTCCTC[A/G]TGAGAGCAGAGCCAT | 66616 |
rs579187096 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5910442 | TTTGTTTGCTTGTGG[A/G]GATGAAAATTTTAAG | 66616 |
rs579187420 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5855937 | GAAAGGGTTGGTGTA[G/T]AGTGATACCTAGAGG | 66616 |
rs579190209 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5890294 | CTAATTAAATAAAGT[G/T]CGGGAAATACATTGA | 66616 |
rs579196273 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5867475 | AAGAAGGGTGTTGCT[A/G]AGTATTGCTAAGATA | 66616 |
rs579197037 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5909452 | CAACCTGCTGCTAAG[C/T]AATCCTGACCTCCTA | 66616 |
rs579199284 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5906442 | TGCAGTCCTCCGCCA[C/G]CTCCTGACATAGGGA | 66616 |
rs579199831 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5904488 | ATGCTCAAACGTTAA[C/T]ATATTACTGTTTACG | 66616 |
rs579201978 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5897449 | CATGTAAAAGAGCGC[A/G]TTCGGTCTTGCACAG | 66616 |
rs579207065 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5870636 | TTGCAAATGAAACCG[G/T]GTTATTTCTCTGTCT | 66616 |
rs579209395 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5902969 | ACAGCTGCACACAGC[A/T]GCACACAGCTGCACA | 66616 |
rs579211743 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5876345 | CATAAGTACATACAT[A/G]ATTATATTCACCCTA | 66616 |
rs579212901 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5885287 | GTTTGTAGCAATGCA[A/T]TCTGAGTGTAGTAGC | 66616 |
rs579213255 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5900240 | GGTGGCCAGGCATGG[A/G]GATATGGCTCAGTGG | 66616 |
rs579221666 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5913795 | TTAGCATCTGTAGGT[C/T]GGGGGTTTATGAACT | 66616 |
rs579223325 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5888603 | TCCACACCAGCTGCT[A/G]TGTCCTCCTAGTTCC | 66616 |
rs579225203 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5892091 | TGGTTGGGGGGATGG[A/G]GTGTGGCGTGGGGGT | 66616 |
rs579231136 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5886674 | CATGCCTGCCTGTGT[A/G]CAATGCCTCCATTCC | 66616 |
rs579237175 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5893389 | GTAATAAAGCTGTGG[C/T]TAGCCTGTGGCTAGG | 66616 |
rs579238497 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5907694 | TGTGTAGCCCTCTAA[C/T]TCAAAGATTTCGGTT | 66616 |
rs579243175 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5894653 | TGGCTCCACCTAGGC[C/T]CTGGAGTTTCCTTTG | 66616 |
rs579248801 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5901314 | CCATCCCATCCACAT[C/T]CCTGCATCCCCTCCC | 66616 |
rs579261370 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5914664 | TTAATTTTTCTAGTA[G/T]TTCTTTGAACATACA | 66616 |
rs579265825 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5908713 | AGGTGAGTTGGAGCA[C/G]TACCGATCAGTATGA | 66616 |
rs579267814 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5869591 | AGCCTTAGGTCTGAC[A/C]CAGAAGTCAAGGTAA | 66616 |
rs579276924 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5875572 | CCTGGACTACCTGAG[A/G]TAGAGTGTGTGTGTG | 66616 |
rs579279224 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5902614 | TGTGTGAGCCCGTGC[A/G]CGTGCATGCATGCAT | 66616 |
rs579283146 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5886014 | ACATTATGAAGCACC[C/T]GTTAAAGCGTGTCGG | 66616 |
rs579289547 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5918684 | GCTGGAGCAGTCAGC[C/T]CAGGGTGGTGGGGCA | 66616 |
rs579293018 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5898633 | ATAAAAGGGATAAGT[C/T]TAAGCAAGTCCAAGA | 66616 |
rs579297251 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5915280 | AGTGTGGGCTCTTTG[C/T]CCTCTTGATGTCACT | 66616 |
rs579300047 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5874221 | TTCATCTTTAAAGTC[G/T]ACTGATTTCTCCCCT | 66616 |
rs579300792 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5892706 | CCTTAATCCCAGGCT[C/T]TCTGTGAGTCCAGGC | 66616 |
rs579306563 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5921652 | AGGGTCTCTGAAGGC[A/G]TCAGAGTGCTCCTCA | 66616 |
rs579308436 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5872886 | AAAATTTTTAAAAGC[A/G]CCCTTGAGATTAGGC | 66616 |
rs579310745 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5911208 | TAGATAGATTCCTCC[C/T]AAGGGTCCTCTGATG | 66616 |
rs579311538 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5912975 | GCCTGGAGCTTGTTA[C/T]TTAACCAGGCTGACC | 66616 |
rs579314545 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5882843 | CTGTATAGGAAGTAG[A/G]CAGCAGACACTGGAG | 66616 |
rs579315406 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5909740 | GGCCTGGGGGAGAGG[C/T]CAGAGGGCCTTGGAG | 66616 |
rs579317744 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5876899 | AGTGGTAGTAGGTTC[A/C]CCACCCCAGCCAGGG | 66616 |
rs579318509 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5899533 | GTGACAGGCAGGGGG[A/C]ATAGGCTGATCTTGC | 66616 |
rs579320238 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5906879 | GTTCTGCACCTTATT[C/T]CCAAATTACAAAGTC | 66616 |
rs579320909 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5905378 | AATAAGGGGCTTTTC[C/T]AGCATGCTGGAGATA | 66616 |
rs579322515 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5903271 | AGAAATATTTTTAGC[C/T]ATAGAAAGCTAAAAA | 66616 |
rs579327465 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5887561 | TGTGCACATAGAGGC[A/G]TTCATCTTCATACAT | 66616 |
rs579329344 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5891108 | GCTTCTTAGATTTGT[G/T]TAATCTTTCAAGACT | 66616 |
rs579330406 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5900555 | CACCCCACCCCGCCC[A/G]AGAAGGATGTTTGTG | 66616 |
rs579333377 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5878758 | TTGGAAGGGTCTTAG[A/G]GTCTTACTCAGGTTG | 66616 |
rs579339048 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5893882 | AGAGATGGCTCAGCG[A/G]GTAAGAGCACTGACT | 66616 |
rs579345205 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5889443 | AGGTTCAATCCCGGA[A/G]ACATAGGACAAAGCC | 66616 |
rs579353776 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5896830 | TGCTGTAGCACGGGG[G/T]AGGCGTGAGGGACAT | 66616 |
rs579381013 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5841920 | CACGCTCCCTCCGCG[C/T]CCACTGCCTTCCAGG | 66616 |
rs579383218 | snp | A/G | | | intron-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5847862 | ATTCTTATTAAAGAA[A/G]GTTTGTTATTATTGC | 66616 |
rs579395709 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5888646 | TAGGCTCCACACCAG[C/T]AGCTGTGTCTCTTGC | 66616 |
rs579433422 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5851036 | CTTTCATATACTGTG[C/T]TGAGTGAGATGGCAG | 66616 |
rs579438352 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5879591 | GTGTATAGGAAGTAG[A/T]CAGTAGACACTGGAG | 66616 |
rs579438477 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5876692 | CTGCAAGCTCATGGA[C/T]ACACTGACCCCGTTC | 66616 |
rs579443628 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5844025 | GAGCTCTGCTTAAGT[G/T]CGCACACAGCTTAGA | 66616 |
rs579448518 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5887277 | AAATTTATTGCGCCT[C/T]TTTTTTGCTGGTGTT | 66616 |
rs579448670 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5894779 | GCTGAGTTTTCCCTT[C/T]GCTATGGTCACAGTT | 66616 |
rs579451296 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5890603 | CGCCCCCTGCTGGTT[A/G]CCTGTAGGTCTCAAG | 66616 |
rs579458637 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5892193 | GGATTGGGGTGTGGC[A/G]TGGGGCTATGCATTG | 66616 |
rs579460357 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5893664 | AAAGTTGTGTCTGTG[G/T]ATGAGAGACAGTACC | 66616 |
rs579483357 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5926327 | CAAGCCAGACAGGAC[C/T]ACACACTGAGACCCT | 66616 |
rs579485821 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5898219 | CATCCAGCAGGGAGA[A/G]AGAGGTTTCTGGGCA | 66616 |
rs579500885 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5919650 | GGGAGACACAGAGCA[G/T]ACACCAAGAAGAGCA | 66616 |
rs579531060 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5850654 | TGAAGCAGATGGTCA[C/T]ATCCTGCCTACTGTG | 66616 |
rs579542133 | snp | A/T | | | upstream-variant-2KB | Snx9 | GRCm38.p3 | 17:5840897 | CCCATGCAGCCTAGA[A/T]GCAGGAAGCCATTGC | 66616 |
rs579560488 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5843793 | AACCAAATCCTGTTC[C/T]TCTGCAAGAGCAGTG | 66616 |
rs579560757 | snp | C/G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5852651 | CATTGAAAATGTAAA[C/G/T]GAGGAAAATACCTAA | 66616 |
rs579563833 | snp | A/G | | | intron-variant, upstream-variant-2KB | Snx9, LOC105246186 | GRCm38.p3 | 17:5848807 | TGTGATTCACTCCTC[A/G]CCAGCAACCCCTCCT | 66616 |
rs579564125 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5922394 | CCCCCCAGACCCCAA[C/T]CCTCCCTCCGATTGC | 66616 |
rs579565265 | snp | C/T | | | intron-variant, nc-transcript-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5845721 | ATAATGTGAAGTGAC[C/T]TACACACTATAGCTT | 66616 |
rs579570139 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5916618 | GTGAAGGCAGCTGCA[A/G]TGCACTCACATACAT | 66616 |
rs579572258 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5861475 | GTGTGTTTTGTTCCC[A/C]TCTTCTAAGATGGAT | 66616 |
rs579575346 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5855194 | TTCATACATATATGT[C/T]TCAAAGTAAAGACTT | 66616 |
rs579576554 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5854256 | TTTACCACACCCAGA[C/T]GACTGGCTCCTTTGC | 66616 |
rs579579952 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5858486 | AGGGCAGCCATGGAC[A/G]TATCAGGGAGTGATG | 66616 |
rs579582113 | snp | A/C | | | intron-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5847501 | ACAGCTCCCCAATGA[A/C]GAATGTTAGTCAAGT | 66616 |
rs579592735 | snp | A/G | | | intron-variant, nc-transcript-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5846530 | TATATATGAGTAATA[A/G]TAAATGCACTGAGGT | 66616 |
rs579594317 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5919168 | CAGCACCATGAAGGA[A/G]GGTAGGATCCAAGAT | 66616 |
rs579599327 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5913567 | GGGTCGTGCTTCGCC[A/T]TTCTCTTGTGACAAA | 66616 |
rs579606832 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5853323 | AGTCAGAACGCCCCA[C/G]TGGGCTTACCAATGT | 66616 |
rs579612015 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5916960 | TGTGCAGGCAAACAC[A/T]CACACACATACAACA | 66616 |
rs579613397 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5925503 | AAGGTAGGGGATGGA[A/T]CTGAAGTGAGTTGGC | 66616 |
rs579613888 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5907527 | GAGTTCTGGGGTCCT[A/G]GCAGACACTGCTTGA | 66616 |
rs579621577 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5901183 | AAAATCTCTTGGCAA[A/G]CTTCCAGTATATAAT | 66616 |
rs579623459 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5921816 | TCTGGTGACTGTGAT[A/G]GCCACATGCACGTGA | 66616 |
rs579623597 | snp | G/T | | | upstream-variant-2KB | Snx9 | GRCm38.p3 | 17:5839970 | ATGGAAAGAAATCAG[G/T]GCAGAAACTCAGGTC | 66616 |
rs579630296 | snp | A/C | | | intron-variant, upstream-variant-2KB | Snx9, LOC105246186 | GRCm38.p3 | 17:5849413 | CTCCCAGTCATCCCC[A/C]CTTTGTCTGCTTCCT | 66616 |
rs579637379 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5851706 | ATGGCTGTGTGTGTG[A/T]GAGAGAGATGACTGT | 66616 |
rs579637464 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5842250 | AAAATTAGTTTCTCC[G/T]GTTCCTTTTTCTTGT | 66616 |
rs579638795 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5910645 | CTAGAAGAGCAGTTA[G/T]TGCTCTTAACCGCTG | 66616 |
rs579639571 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5872322 | TGCAGTTCCTCTCCA[A/G]AGCAATGGACACTCT | 66616 |
rs579640679 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5914372 | CATTGCCCATGGGGC[C/T]AGTTAGCCATCAGAT | 66616 |
rs579644126 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5920380 | TAGGCATCATGCTGG[C/T]TGTCTTCTGTAAAGT | 66616 |
rs579646492 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5915868 | AGCTAGCTTTACAAC[A/G]AACGCCTCGTTGGTC | 66616 |
rs579647403 | snp | A/T | | | intron-variant, nc-transcript-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5848276 | TCGTCTTCTTCTTCC[A/T]CCGTCTTCCTCCTCC | 66616 |
rs579648669 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5908208 | TGAGAATGGGATGGG[C/T]GCTGTAAGTGGGTGC | 66616 |
rs579650393 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5909982 | CGCTGTTCTTACAGG[A/C]AGGCACTTTCTTTCT | 66616 |
rs579651618 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5844943 | GGTGGAATGGTTTTG[A/T]TTTTTGAGGCAGGGT | 66616 |
rs579654306 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5855976 | TATGTGCATGTGTAC[A/G]TGTGTGCACATACTA | 66616 |
rs579660432 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5861144 | GCTCTGGGATACTGG[C/T]TAGTTCATATTGTTG | 66616 |
rs579663772 | snp | C/T | | | upstream-variant-2KB | Snx9 | GRCm38.p3 | 17:5841047 | GGGATCACCGTTCTC[C/T]GGCTCGCAGAGAGCC | 66616 |
rs579664305 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5904239 | CTTTGTGCTCTAAAT[C/G]TCATTCCAGGTTGAA | 66616 |
rs579664920 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5854635 | AGATAAGAAGTCAAC[A/G]ATTTCCACACCGCCG | 66616 |
rs579666300 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5921926 | GTTCAGAATAAAGTG[C/T]GCTGCTAGTTGAGCA | 66616 |
rs579671091 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5857509 | TGATGTGAAGTATAC[A/G]TTTCATGCTAGCCTT | 66616 |
rs579673431 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5869072 | TGAGTCCTGTGCATG[C/G]AAAGCTGAAAGGCAA | 66616 |
rs579683187 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5864124 | TCAGACACATAGTGA[G/T]CATGGGAACCAGACA | 66616 |
rs579685053 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | Snx9, LOC105246186 | GRCm38.p3 | 17:5848869 | AACACCAGGACTCCA[A/C/G]GACACGTTGTTGATG | 66616 |
rs579696342 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5874968 | TGGGTTTTACAAACT[A/G]AGGAGCACAGTAGCT | 66616 |
rs579703413 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5885309 | TGTAGTAGCAGCTCC[C/G]TTAGGTTCCTGCTCA | 66616 |
rs579708070 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5919213 | CGTAGGGAGGTGCCA[A/C]GTCCACAGTAAAGGC | 66616 |
rs579710789 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5905539 | CTTTGGTTTCATCCC[A/G]TACTTCGGTTGTTAG | 66616 |
rs579714904 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5855286 | AGGCGTGGTGGCGTA[C/T]GCCTTTAATCCCAGC | 66616 |
rs579725088 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5899854 | CCAGGCTGACTGACC[A/G]TGGTCGCTACCACCA | 66616 |
rs579728189 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5852686 | AATAAAATAAAATTT[A/T]AAAAAAAGAAAAAAA | 66616 |
rs579732325 | snp | C/T | | | intron-variant, nc-transcript-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5845837 | GTATTAGTAATGCTT[C/T]GAAATATAACTGATC | 66616 |
rs579737889 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5858818 | GACACTAACAAAATG[G/T]GGTAGAGGGGCAGTA | 66616 |
rs579741690 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5868283 | CCCAACCATATCCTC[C/T]CTGGAGCTAGTTCCT | 66616 |
rs579747865 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5909024 | CAGACCCCAACATGA[C/G]TCAGGCTCTGCCGCC | 66616 |
rs579750421 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5914708 | TTTTTGTCCACTAAG[C/T]TTGACATCTAGCAAC | 66616 |
rs579750851 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5911300 | GCACATCCATCCCAG[G/T]GGTCCCGTGGGTGCT | 66616 |
rs579756108 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5902830 | CAGCGGCACACAGCT[G/T]CACACAGCAGCACAC | 66616 |
rs579756531 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5908944 | AGTACATTTTTTTTA[A/T]GTGTGAGATGGTACC | 66616 |
rs579763374 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5874452 | ACCTACACACACACA[C/T]ATATGCACTTACACA | 66616 |
rs579763471 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5889636 | CCAAGCCAGTGGCCT[G/T]GGCTGATGACCGCAG | 66616 |
rs579764789 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5905488 | ACAGTGCAATCTGTA[A/G]TAGTGAGATGATTGC | 66616 |
rs579770620 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5902799 | AAAAAGTCTTCAAAC[C/T]GGGCACAGCAGCACA | 66616 |
rs579775485 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5884829 | GTGTATAGGAAGTAG[A/G]CAGTAGACACTGGAG | 66616 |
rs579776019 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5899729 | ATTTGACTTCCTGTC[A/G]CCCGTTTATTGCTAA | 66616 |
rs579777010 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5867143 | TGGAGAGTGTGCAGG[C/T]CGTCTGTGGGAAGGG | 66616 |
rs579779153 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5897066 | CTGTATGCATTTATC[C/T]GTTCATACTTAACAG | 66616 |
rs579782959 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5861654 | CTCACTCAGGATGAT[A/G]TCCTCCAGATCCATC | 66616 |
rs579785690 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5871811 | TTTTCTCTAGGATGT[A/G]TGTGGTTAATGCGTT | 66616 |
rs579791410 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5877349 | TAATTCATTTTTTTA[A/G]CTAGGAAATTTCTTA | 66616 |
rs579796660 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5869823 | AAAGGAAGAGGAGGT[A/G]GGGATTGTGTCCTCT | 66616 |
rs579800807 | snp | C/T | | | intron-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5847310 | TGAGACTAGGGATTT[C/T]TATTTACTCTTGATT | 66616 |
rs579803210 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5893026 | TATTGCTTGGTTCTC[G/T]ATCACTTTCTAGTCC | 66616 |
rs579804182 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5875757 | GCCCTGAGCTATCCC[A/G]TACCTGCTGTCCCAG | 66616 |
rs579804248 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5900818 | AGTTTAGAAGTTACT[C/T]GGAGCAGAAAAAACA | 66616 |
rs579804625 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5843573 | TTAGTGCTTATGGGA[A/G]AATGGCTTTAATTCT | 66616 |
rs579806959 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5923299 | GCACCCTTCACCAAA[A/G]TGAGCCAGGTGCCTC | 66616 |
rs579807791 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5857522 | ACGTTTCATGCTAGC[C/T]TTCTATAAGTGAGTC | 66616 |
rs579810500 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5926827 | ACAACAAAGGAAAGC[A/C]CTGCAGTCTGCACAG | 66616 |
rs579810810 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5872995 | GCTAGTTTTGTGTCA[A/G]CTTGACACAGCTGGG | 66616 |
rs579811141 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5878806 | CATCTTTAGCCCTAC[A/G]CTGCAGAGTTGCTTA | 66616 |
rs579811399 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5888052 | AGAGAGTGCAGGCCC[A/C]CAGCCTTCTGCCTGT | 66616 |
rs579814672 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5917124 | CGTCCCCCTCATCCT[A/G]CCCCTGTGTGTGCGT | 66616 |
rs579820685 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5920525 | GTGTTTGGTCTGTGT[G/T]TCTCTGGCATTGCTG | 66616 |
rs579820852 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5914716 | CACTAAGCTTGACAT[C/T]TAGCAACACTTGGTG | 66616 |
rs579821351 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5886027 | CCCGTTAAAGCGTGT[C/T]GGAGCTTTAAGTACC | 66616 |
rs579823409 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5861868 | GATCATCTTCTGGGT[A/C]TATTCCCAGGAGTGG | 66616 |
rs579826367 | snp | A/G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5903019 | ACAGCAGCACACAGC[A/G/T]GCACACAGCAGCACA | 66616 |
rs579829584 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5870808 | TCCACCACGGAACAG[C/T]GGCCGTGCATTAGGT | 66616 |
rs579833634 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5911408 | ATCCTCAGTGTCAGC[A/G]CACCTACAGACCTCT | 66616 |
rs579839136 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5876493 | CACTGAATGCAATTA[A/G]TGCTGTCCATATATG | 66616 |
rs579844417 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5912276 | TTTTTTTCTCCAGTC[C/G]AGTTCAGTGTGTCCC | 66616 |
rs579850836 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5854796 | AGAACTGGGTCAGAA[G/T]GTTCCTCTGAGCTTA | 66616 |
rs579856163 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5867657 | TTTCCTCAAGAGAGG[C/T]ACACTCAGTTTGCAC | 66616 |
rs579856347 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5906499 | CCTGCACAGAATGAG[A/G]GGTGGATATTCTTCC | 66616 |
rs579862604 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5873376 | CTAAGACAGTACCTG[C/T]CAGAGATCATTAGCA | 66616 |
rs579867116 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5900314 | TTTTCCAGTACTCAC[A/G]CAGCAGCTAAGATTT | 66616 |
rs579868822 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5892201 | GTGTGGCATGGGGCT[A/G]TGCATTGTGAGGGTG | 66616 |
rs579880090 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5879437 | GAAGTAGACAGCAGA[C/T]ACTGGAGCTGAGGCC | 66616 |
rs579889483 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5861166 | ATATTGTTGTTCCTC[C/T]TATGGAGCTGCAAAC | 66616 |
rs579899579 | snp | A/G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5888838 | GATTATTCTCATAGC[A/G/T]TTGCTTTTTGGCCCT | 66616 |
rs579908978 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5872535 | GTGGTTCTAATCTCT[C/G]TGTCTCTCACTCCAT | 66616 |
rs579911304 | snp | C/G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5864305 | TAGTGAGCATGGGAA[C/G/T]CAGATACATAGTGAG | 66616 |
rs579913010 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5869159 | TGGGATTCCTCTGCA[C/T]AAGGAAGGCCAGTGT | 66616 |
rs579914991 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5894790 | CCTTTGCTATGGTCA[C/T]AGTTCCCTGCTGTTT | 66616 |
rs579917570 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5875059 | TCGCAGGCACATGCT[A/G]TTATCCTTATCTTAT | 66616 |
rs579922068 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5887176 | TCGGTGTTTCAGCTG[G/T]TGCTTATGAAATGCT | 66616 |
rs579925831 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5894264 | CCTGGGTTGGCTGGA[C/T]GATAGTCTCCCTCCA | 66616 |
rs579931683 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5890403 | CGCCCGCCCGCCTCC[A/G]GCTTGGAGGTGGATT | 66616 |
rs579932740 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5899203 | TTCTGCCTGAGTGAC[A/T]AGCAGGGGGAGTAGG | 66616 |
rs579933541 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5878293 | AAAACAGTCTCACAC[A/T]CACACTCACACACAC | 66616 |
rs579937731 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5893570 | ATTCTCACTAATTCT[C/G]AGCCATGGTCCACTT | 66616 |
rs579943139 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5898042 | GGATGTTATGCACAG[A/G]CAATCGCTTCCTGTT | 66616 |
rs579952580 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5905071 | TTTGGAAGTATTTTT[A/G]AGCATACGTATCCTG | 66616 |
rs579956590 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5901900 | TTATCTTTGCTTCAG[G/T]TCCCTGACTCTGGTG | 66616 |
rs579981973 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5925746 | TTTTATTGATTAAAA[A/G]TGGCCCAGGACACAT | 66616 |
rs579988672 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5891456 | ATTAACCAGTCACAG[A/C]GTGCTTCTCAGAGTA | 66616 |
rs580036386 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5886241 | TACTGGCTGCTGGCT[A/G]CTGGCTGCTGCCTGC | 66616 |
rs580039639 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5889676 | GGAGAAGGAGAGAAC[C/T]TACCTCCTGAGTTGT | 66616 |
rs580045494 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5920698 | GTGACTCGGCCTTCA[C/T]GAGTTAAAACCAGAA | 66616 |
rs580047235 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5893149 | GTTGTGAGCAGGAAA[C/T]GCTAACTTTCCACTC | 66616 |
rs580050429 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5926850 | CTGCACAGCCAAGCC[C/T]GGCTCGCTCGTAAAT | 66616 |
rs580074455 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5914757 | TTGACTTTTTTTTTT[C/T]TCCTTCAATTTAGAG | 66616 |
rs580076305 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5856239 | CTCCCTTCTGGCCCA[C/T]CACTTACCAGAGGTA | 66616 |
rs580085645 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5909178 | CCCAGCCTTTCTTGT[C/T]TATTTAAAAGGCTCC | 66616 |
rs580093482 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5923499 | GCAGTTCTGAAACTG[A/T]AACGACAGGCACACG | 66616 |
rs580097541 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5917167 | GTGTGTGTGTGCGTG[C/T]GTGTCTGTGTGTGCG | 66616 |
rs580109754 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5911489 | TCCTTCCTTCTAGCC[A/G]TCCTGTTTGCTTTAT | 66616 |
rs580122871 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5859869 | TGCAGGAAAACCCAG[C/T]GTCGGCTCTGCGGCA | 66616 |
rs580128749 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5905807 | ATATGTAAAAAGCTT[C/T]AAACTCTAGGAACCT | 66616 |
rs580145552 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5924296 | GGTGGAGCCACCCAC[A/G]GTGAGCTGGGCCCTC | 66616 |
rs580145855 | snp | C/G | | | intron-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5847439 | TTGCCTCTCCTAGTC[C/G]CTAGGCTTTGGGGAG | 66616 |
rs580148835 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5925397 | GTGTGTGTGTGTGTG[G/T]GTGGGGGTCCTGTGG | 66616 |
rs580152744 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5919077 | ACCCGGCTGTGGGGA[A/G]GGTAAACCCCAAATG | 66616 |
rs580160716 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5921794 | CCTTCCATATGGAGA[C/T]GGTGTGTCTGGTGAC | 66616 |
rs580169233 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5915692 | ACACACCTTCTGGTG[A/G]TGTAGTGGCAGCGAC | 66616 |
rs580172164 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5918147 | CACACACTTCGCACA[C/T]GTGCGCGCGCACACA | 66616 |
rs580177281 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5913401 | TTTTTAAAATAGAAT[G/T]TATTAGTCTATTTGT | 66616 |
rs580177326 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5909968 | CCGGGTACTTTCCTC[A/G]CTGTTCTTACAGGCA | 66616 |
rs580180164 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5912493 | AGATTTACTTCTGAA[G/T]GAAAGTTGAGGCTGC | 66616 |
rs580190060 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5858945 | ACTGTGGAATGGGGC[G/T]GGGCTAGGTTTTCAG | 66616 |
rs580192951 | snp | G/T | | | intron-variant, upstream-variant-2KB | Snx9, LOC105246186 | GRCm38.p3 | 17:5849505 | ATACCCTCCTTCCCC[G/T]GCTCCACACCTCAGC | 66616 |
rs580193930 | snp | A/G | | | intron-variant, nc-transcript-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5846738 | CGCATGGGTGTCTGT[A/G]CTCACATCAGTAACA | 66616 |
rs580198094 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5843717 | TGTTCCAAGAAGAGG[C/G]ATCTGGATTCCCTGG | 66616 |
rs580201373 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5842311 | AGCCACCGGGAAAAG[C/T]CTAAGCCTTGGAAGT | 66616 |
rs580202178 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5927895 | TTTCTAGAGGTGTGC[A/G]TGTGTCAGAGAAAAG | 66616 |
rs580204334 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5921230 | GCCTGAGCTTTTACT[C/T]CCCCTGCATTCCCCA | 66616 |
rs580218658 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5850447 | AGGGACAGGGTTCTC[A/T]GCTCGGATTTCAGAT | 66616 |
rs580220034 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5867161 | TCTGTGGGAAGGGCA[G/T]AGGAATGACAAACTT | 66616 |
rs580221658 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5853457 | CAGTGCGTCTGGTGT[C/T]GTCCAAACATGTAGG | 66616 |
rs580222416 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5873066 | CATGAGATCCAACTG[C/T]AAGGCATTTTCTCAA | 66616 |
rs580222984 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5915084 | TTGGCCTGACTTGAA[C/G]GGCAGAGCTCTACCT | 66616 |
rs580226446 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5877073 | GCCCATCAGAAACTG[C/G]TAAGACTGTTGCTGA | 66616 |
rs580227137 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5909516 | AACTTGGCATGGCGG[A/C]GCTGAGTGTCCTCCG | 66616 |
rs580229099 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5855529 | AAACAGCGCCATCTC[A/G]TTAATTTAGATATTC | 66616 |
rs580232369 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5887895 | AAAGCTGTTTGAAAT[A/C]AAAGTTCTGAGGAAA | 66616 |
rs580253262 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5870046 | ATTTGTAGTGATGGA[A/G]GCAATTGAGTGAGTG | 66616 |
rs580255215 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5861661 | AGGATGATATCCTCC[A/G]GATCCATCCATTTGC | 66616 |
rs580262697 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5854622 | CCGGGGTCCACCCAG[A/T]TAAGAAGTCAACGAT | 66616 |
rs580264476 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5926447 | ATTTAATGCTGGTTA[C/G]CATTTCCTCTCAGGG | 66616 |
rs580265672 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5916603 | CCCCTTCTGGTGTGT[C/G]TGAAGGCAGCTGCAG | 66616 |
rs580265957 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5842464 | GATTTATTTTTGACA[C/T]GTCTAAGCTACTTCT | 66616 |
rs580267950 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5884569 | CACTGGAGCTGAGGC[C/T]GTGTGTATAGGAAGT | 66616 |
rs580269291 | snp | C/T | | | intron-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5848225 | ATAAGATATTCATAG[C/T]TACCTGTGGCTGTTT | 66616 |
rs580271390 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5861089 | TGGAGCCATGAGTCC[C/T]ACCATGTGTGCTCTT | 66616 |
rs580274112 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5922545 | CTCTGAATGAACACA[C/G]ACCCGGCAGTCCTCT | 66616 |
rs580280767 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5910619 | GTTGCTGGGAATTGA[A/G]CTCAGGACCTCTAGA | 66616 |
rs580280809 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5875842 | GTGAGGCCAGGCTGG[C/G]CCACGCGAGACCCTG | 66616 |
rs580285192 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5924525 | CTAAAACTATCAATA[A/G]AGTCTGTAACAAAAA | 66616 |
rs580285764 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5906521 | TATTCTTCCTGCCCC[C/T]AGCGTGTACTGGCCT | 66616 |
rs580288423 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5919796 | TTACTCTATGTGTCC[C/T]GTATAGAGTGCACAT | 66616 |
rs580288574 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5900460 | TCTTGAGGAACAGTA[C/T]CCAAGGTTGTCCCCC | 66616 |
rs580290581 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5868988 | TCTCAGCACTTCCTC[C/T]TCCTCACACAGTCAC | 66616 |
rs580291733 | snp | A/G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5903039 | ACAGCAGCACACAGC[A/G/T]GCACACAGCTGCACA | 66616 |
rs580292608 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5904815 | AGGGTTAAAACTGGT[A/G]TGGTAAGGTCACATG | 66616 |
rs580294449 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5914512 | TTACAGAGCTGGGCT[C/T]TGCCAGCTTGTGTTT | 66616 |
rs580295988 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5900384 | GGCTGTGTGGGCACT[G/T]CGTGCACATGGCACA | 66616 |
rs580298015 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5916627 | GCTGCAGTGCACTCA[C/G]ATACATAAAAGTCTT | 66616 |
rs580301623 | snp | C/G | | | intron-variant, upstream-variant-2KB | Snx9, LOC105246186 | GRCm38.p3 | 17:5848941 | GTGTGATGAGTTCTG[C/G]ACTGCTCAGCGTCTC | 66616 |
rs580301817 | snp | A/T | | | intron-variant, nc-transcript-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5846791 | TTGAGTCGGTGAGAG[A/T]GTCTGGGCTGTAGAA | 66616 |
rs580303438 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5851490 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 66616 |
rs580305963 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5854195 | GTAGGCCGTGGCTGG[A/G]GCCTTGTATTGATTT | 66616 |
rs580308212 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5856893 | TGCTTGCTTTAGTAG[A/T]GCATCCTTTCACCCG | 66616 |
rs580312084 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5910682 | CTCCAGCCCCTGAAA[A/G]TTTTAGTTTTTATTT | 66616 |
rs580315442 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5919589 | TGGACAATGGGAGCT[A/G]GGGAAACCCAGAGCA | 66616 |
rs580316120 | snp | C/T | | | intron-variant, nc-transcript-variant | Snx9, LOC105246186 | GRCm38.p3 | 17:5846093 | AAAAATTTGTCGAGC[C/T]TAAGCTTATGCTTAG | 66616 |
rs580317386 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5914238 | AGCCCCTAACCAGTG[A/T]ACCATCTCTCCAGCC | 66616 |
rs580322564 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5862782 | ACATTCCAGAAGAGG[C/G]CGTCAGATCTCATTA | 66616 |
rs580323013 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5878900 | GTGTATGTGTGTGGG[A/G]GTAAGGATCAGACCC | 66616 |
rs580323610 | snp | A/G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5864075 | GCAGACACATAGTGA[A/G/T]CATGGGAACGCAGAC | 66616 |
rs580327741 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5844579 | AAACCCCTATCTGAA[A/G]CTTCTTAAGAATTAA | 66616 |
rs580328343 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5857495 | ATCTGATAAGTTGCT[A/G]ATGTGAAGTATACGT | 66616 |
rs580330608 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5908053 | ATCTTCTGTACTCCA[A/G]CTTTCTGAATGTGAG | 66616 |
rs580333715 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5926259 | AAATGTGGTGGTGCA[C/T]GCCTGTAATCCCAGC | 66616 |
rs580334352 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5868178 | ACAGTGAGGCCATGG[A/G]TGGGAAGGCCATGCT | 66616 |
rs580335391 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5890465 | GGCCAGGCTTCACGC[A/T]TCCTTCTGCTGCTTT | 66616 |
rs580336092 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5852918 | CCAGCTGTACACTCT[C/T]GGGCTTCACCATTGT | 66616 |
rs580337594 | snp | C/T | | | upstream-variant-2KB | Snx9 | GRCm38.p3 | 17:5839817 | TCCTCTGACTTCACA[C/T]GTGCTATATGCATGT | 66616 |
rs580338020 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5918150 | ACACTTCGCACATGT[A/G]CGCGCGCACACACAC | 66616 |
rs580339741 | snp | G/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5860421 | CTCCCCATAAATAAG[G/T]GGCAGGGGACAGCCA | 66616 |
rs580340657 | snp | A/C | | | intron-variant | Snx9 | GRCm38.p3 | 17:5921266 | GTGGGGCTGTGGGTT[A/C]CCAGAACAGAATAAG | 66616 |
rs580345162 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5915111 | ACCTAGCTTACCTTT[A/T]GGCAATGGAAAGACA | 66616 |
rs580346046 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5871495 | TTTTTGTCAATATTA[C/T]TGATTTGTGTTTTTG | 66616 |
rs580346571 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5901656 | GGATCCTCTAGAGCC[A/G]GAGTTACATACCACT | 66616 |
rs580349113 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5922268 | GATTGTCCCCCTTGA[A/G]TCACGTGAGCACGTG | 66616 |
rs580352368 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5872240 | TTCTGTGTGTATGTG[C/T]ACATGGCTGCATGTG | 66616 |
rs580352970 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5898189 | GTGAGCTGAGGCAGG[A/G]AATAGGAGGTGGGAC | 66616 |
rs580360167 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5874404 | ATGCACCTACACACA[C/T]ACATATATGCACTTA | 66616 |
rs580361627 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5912666 | TGGTGCTCAGTGTTA[C/G]ATTTTAGCTCCTTCC | 66616 |
rs580362913 | snp | C/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5876601 | TAGGAGCTAGCAACT[C/G]TGAGCAGGTCCTTAG | 66616 |
rs580366007 | snp | A/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5909643 | GAGTAGTAGGTAGAA[A/T]GTGTTCAGATGGCGA | 66616 |
rs580367234 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5906601 | TGCTCCTCTTCTGCA[C/T]GTCCTCATCGCTGCT | 66616 |
rs580373193 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5903087 | ACAGCTGCAATGCCA[A/G]CACTCGGCAGGTACA | 66616 |
rs580381987 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5887221 | CTGTCACATGCACAC[C/T]TAGAGAAGTTCAGCC | 66616 |
rs580386025 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5862799 | GTCAGATCTCATTAC[A/G]GATGGTTGCTGGGAT | 66616 |
rs580392232 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5893651 | CCCTTCTTCTCCTAA[A/G]GTTGTGTCTGTGTAT | 66616 |
rs580394015 | snp | C/T | | | intron-variant | Snx9 | GRCm38.p3 | 17:5856947 | TTCACTCCTTTAAGT[C/T]CCCACATCACATCCG | 66616 |
rs580421160 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5856255 | CACTTACCAGAGGTA[A/G]TGGGAAGAAAGGATA | 66616 |
rs580427241 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5853702 | TCTCTCAGTAGTTTC[A/G]TCAAACACTTATTGG | 66616 |
rs580429166 | snp | A/G | | | intron-variant, upstream-variant-2KB | Snx9, LOC105246186 | GRCm38.p3 | 17:5849626 | CTGACGCTGCAGCTC[A/G]GGTTGTAGGCGCTGC | 66616 |
rs580431260 | snp | A/G | | | intron-variant | Snx9 | GRCm38.p3 | 17:5861931 | ACTTTCTGAGGAACC[A/G]CCAGACTGATTTCCA | 66616 |