SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs27087115 | snp | C/T | 0.426035 | 0.177515 | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | GRCm38.p3 | 11:95844067 | CAGGCAGTACGAATG[C/T]TTTCCGTGCGTTATT | 66610 |
rs27087116 | snp | A/C | 0.493827 | 0.0552116 | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | GRCm38.p3 | 11:95843971 | CAGGCTGGCTCTCTC[A/C]TGGTTGCCTGGAGTT | 66610 |
rs27087117 | snp | C/G | 0.495868 | 0.0452663 | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | GRCm38.p3 | 11:95843680 | TGGCCTGTTTTAGAA[C/G]GTTAGTGTCTGCTGT | 66610 |
rs27087118 | snp | G/T | 0.426035 | 0.177515 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Gngt2, Abi3 | GRCm38.p3 | 11:95843388 | GTTGAGCATTGGAAC[G/T]GAGGGTGTGTCTTTA | 66610 |
rs27087119 | snp | A/G | 0.197531 | 0.244432 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Gngt2, Abi3 | Mm_Celera | 11:95843315 | CTCCAGGGAGGACAC[A/G]GAGGCCAAGAAGCAA | 66610 |
rs27087120 | snp | A/G | 0.426035 | 0.177515 | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | GRCm38.p3 | 11:95842849 | GTAGGAGAAGGTGAA[A/G]TTGACCAAATAACTA | 66610 |
rs27087121 | snp | C/G | 0.429688 | 0.173817 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | Gngt2, Abi3 | GRCm38.p3 | 11:95842761 | GACACAGCTAGAGTT[C/G]CTGAATAACTGTGGG | 66610 |
rs27087122 | snp | A/C | 0.408163 | 0.193609 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Gngt2, Abi3 | GRCm38.p3 | 11:95842456 | GATTGCTCCCTGGTC[A/C]TGGAGAGGAAGCTAG | 66610 |
rs27087123 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Gngt2, Abi3 | GRCm38.p3 | 11:95842263 | CTCTGCGTGAGAGAC[C/T]CAAACCTGCCTGTAA | 66610 |
rs27087124 | snp | A/G | 0.260355 | 0.249785 | upstream-variant-2KB, intron-variant, synonymous-codon | Gngt2, Abi3 | Mm_Celera | 11:95842072 | TAGCAGGGCGCTGTG[A/G]TTGCCCCGCAGAGCC | 66610 |
rs27087125 | snp | C/T | 0.459184 | 0.136902 | upstream-variant-2KB, intron-variant | Gngt2, Abi3 | GRCm38.p3 | 11:95841983 | CTATGCTGCAGGTCC[C/T]TGTGAGGTGTATCCT | 66610 |
rs27087126 | snp | A/G | 0.260355 | 0.249785 | upstream-variant-2KB, intron-variant | Gngt2, Abi3 | Mm_Celera | 11:95841861 | CTGAGGCTATGGCCC[A/G]AGAACAAGGGCTATG | 66610 |
rs27087127 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Gngt2, Abi3 | GRCm38.p3 | 11:95841756 | TGTTCTGGTTCCCCT[A/G]GAGCCAGCTTAAAGA | 66610 |
rs27087128 | snp | A/T | 0.345679 | 0.230967 | upstream-variant-2KB, intron-variant | Gngt2, Abi3 | GRCm38.p3 | 11:95840924 | TGCTTTGCTTTGCTC[A/T]GTAAGAGGTTGCAGA | 66610 |
rs27087129 | snp | C/T | 0.391111 | 0.206368 | upstream-variant-2KB, intron-variant | Gngt2, Abi3 | GRCm38.p3 | 11:95840830 | TTTGCTCTGCCATTT[C/T]CCATAGGCCTTCGGG | 66610 |
rs27087130 | snp | G/T | 0.497778 | 0.0332592 | upstream-variant-2KB, intron-variant | Gngt2, Abi3 | GRCm38.p3 | 11:95840712 | GTCCCTTTCCAAAGG[G/T]CAGCTTTCTCATTGT | 66610 |
rs27087131 | snp | C/T | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Abi3, Gngt2 | GRCm38.p3 | 11:95840357 | AACCACATGTCAGAT[C/T]ATCAGGCTGGTCACT | 66610 |
rs27087132 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Abi3 | GRCm38.p3 | 11:95840207 | ATCCTGCGTGCACAC[A/G]AATTACACATGTGGG | 66610 |
rs27087133 | snp | A/G | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Abi3 | GRCm38.p3 | 11:95839813 | ACTTGTAACCAGCCT[A/G]GAGAAGGTATAGAGT | 66610 |
rs27087134 | snp | C/T | 0.493827 | 0.0552116 | intron-variant, upstream-variant-2KB | Abi3 | GRCm38.p3 | 11:95839442 | GTCAACCCTGACCTA[C/T]GCTGACCCATCTGCC | 66610 |
rs27087135 | snp | C/T | 0.165289 | 0.235211 | intron-variant, upstream-variant-2KB | Abi3 | Mm_Celera | 11:95839421 | ATGACCCTGTTTTTA[C/T]GCTCAGTCAACCCTG | 66610 |
rs27087136 | snp | C/T | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Abi3 | Mm_Celera | 11:95839081 | TGTTCATTTGTGTGC[C/T]GATTTACATGTCATC | 66610 |
rs27087137 | snp | C/T | 0.359862 | 0.224567 | intron-variant, upstream-variant-2KB | Abi3 | GRCm38.p3 | 11:95838951 | AAGAGTTGTATCCTC[C/T]GTGAGATTCCTCTGG | 66610 |
rs27087138 | snp | A/G | 0.260355 | 0.249785 | intron-variant, utr-variant-5-prime | Abi3 | Mm_Celera | 11:95837762 | TAGGAACCGAGAGAT[A/G]GGCAGCGTGTCCCAG | 66610 |
rs27087139 | snp | A/G | 0.459184 | 0.136902 | synonymous-codon | Abi3 | GRCm38.p3 | 11:95835895 | AGAGGGCAGCCGCAC[A/G]ACAGTGGCCAAAGTG | 66610 |
rs27087140 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Abi3 | GRCm38.p3 | 11:95832898 | GGCAAGAAGAGAACC[G/T]TGTGAGGTGTCCCCT | 66610 |
rs27087141 | snp | C/T | 0.495868 | 0.0452663 | utr-variant-3-prime | Abi3 | GRCm38.p3 | 11:95832699 | GGGTTGGTGCAGGGA[C/T]AGATCCTGGGCTGTC | 66610 |
rs27087142 | snp | A/T | 0.46875 | 0.121031 | utr-variant-3-prime, downstream-variant-500B | Abi3, Phospho1 | Mm_Celera | 11:95831893 | AAAGTCAGAAGGAAC[A/T]ACCGCCTCCTGCTGG | 66610 |
rs27087143 | snp | C/T | 0.35503 | 0.226867 | utr-variant-3-prime, downstream-variant-500B | Abi3, Phospho1 | Mm_Celera | 11:95831892 | AAAAGTCAGAAGGAA[C/T]TACCGCCTCCTGCTG | 66610 |
rs27087144 | snp | A/G | 0.426035 | 0.177515 | utr-variant-3-prime, downstream-variant-500B | Abi3, Phospho1 | Mm_Celera | 11:95831735 | CCTATGATGCTCTCA[A/G]AAGACAGCTCTAGGT | 66610 |
rs27087145 | snp | C/T | 0.429688 | 0.173817 | utr-variant-3-prime | Abi3, Phospho1 | GRCm38.p3 | 11:95831333 | GCCTGCCAGGGGTGC[C/T]CGGGACAACCGACGG | 66610 |
rs27087146 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime, synonymous-codon | Abi3, Phospho1 | GRCm38.p3 | 11:95831267 | CTGGGAAACAGCCGC[C/T]GATGTGCGCCAACAT | 66610 |
rs27087147 | snp | C/T | 0.415225 | 0.187619 | utr-variant-3-prime, synonymous-codon | Abi3, Phospho1 | GRCm38.p3 | 11:95830730 | GTACATGCAACGAGT[C/T]TTTAAGTACCTGGGT | 66610 |
rs27087148 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, synonymous-codon | Abi3, Phospho1 | GRCm38.p3 | 11:95830652 | CTCGATCGTGCGTGC[C/T]GCGCCAGGCCAGCAA | 66610 |
rs27087149 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime, intron-variant | Abi3, Phospho1 | GRCm38.p3 | 11:95830481 | CGCTAATCAGCTTCT[C/T]CCTGGCCGGCTCCCG | 66610 |
rs27087150 | snp | A/G | 0.142012 | 0.225474 | downstream-variant-500B, intron-variant | Abi3, Phospho1 | Mm_Celera | 11:95829919 | CTCCCAGGGTCTTGT[A/G]TGGTTTGCATACCTA | 66610 |
rs29392269 | snp | A/G | 0.444444 | 0.157135 | missense | Abi3 | Mm_Celera | 11:95833735 | GGTGCTACAGGTGGA[A/G]GAGGCGGGGTTGCAG | 66610 |
rs29395389 | snp | G/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Abi3 | GRCm38.p3 | 11:95838891 | CCCCTGTGGCCTCCT[G/T]GCTTGGGATTTTGTG | 66610 |
rs29397516 | snp | A/C | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Gngt2, Abi3 | GRCm38.p3 | 11:95841416 | TCCCAGCACTGAGGG[A/C]AGGCTGAGACAGGAG | 66610 |
rs29404719 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant | Abi3, Phospho1 | GRCm38.p3 | 11:95830110 | CCTGGCTCCTCCATT[C/T]ATTCTTGATCCCAGG | 66610 |
rs29406198 | snp | A/G | 0.444444 | 0.157135 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | Gngt2, Abi3 | GRCm38.p3 | 11:95842676 | GGGGGGTGGGGCTGG[A/G]CTGGCAGTACAGCTC | 66610 |
rs29412223 | snp | A/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Abi3, Gngt2 | GRCm38.p3 | 11:95840488 | GATTTTGCTTTGCTG[A/T]GTTTGGTTTATTGGA | 66610 |
rs29412315 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Abi3 | GRCm38.p3 | 11:95835473 | CCCCTCTTCCCCTTC[A/C/T]CACACACACACACAC | 66610 |
rs29412439 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Abi3 | GRCm38.p3 | 11:95834847 | TCCCCAAATTCAAGG[C/T]AGAGGGATGGCAGAA | 66610 |
rs29412838 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Abi3 | Mm_Celera | 11:95833554 | TGTAAAATAGTCTAT[C/T]TACTGCTTCTCTGGG | 66610 |
rs29413305 | snp | A/G | 0.5 | 0 | intron-variant | Abi3 | GRCm38.p3 | 11:95836441 | CTGTCCCCTTCAGGG[A/G]ACAAGTACGGGAATT | 66610 |
rs29418656 | snp | A/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Abi3 | GRCm38.p3 | 11:95839529 | AGACATCACCCCAAA[A/T]TTTTCCTCTGTAGAC | 66610 |
rs29423206 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Gngt2, Abi3 | GRCm38.p3 | 11:95841553 | GCCACACAGTGAGAC[C/G]CTGTCTCAAAATCCA | 66610 |
rs29427696 | snp | A/G | 0.375 | 0.216506 | intron-variant | Abi3 | GRCm38.p3 | 11:95835676 | GGAGAGGAAGAAGGG[A/G]ATGTGAGGTCGTACA | 66610 |
rs29429863 | snp | A/G | 0.5 | 0 | intron-variant | Abi3 | GRCm38.p3 | 11:95836633 | TGAGAGTATTTATGA[A/G]CCAAGGGTAGGTATT | 66610 |
rs29429896 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Abi3 | Mm_Celera | 11:95833883 | CAGACCTCATAGTAA[A/G]ATCTGCATTAATTTT | 66610 |
rs29433396 | snp | A/C | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | Abi3, Phospho1 | GRCm38.p3 | 11:95832520 | TATGCCATCTGCAGC[A/C]GTCCCCCCTGAGTAC | 66610 |
rs29434345 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant | Abi3, Phospho1 | GRCm38.p3 | 11:95830297 | ACCGAAGCCAAGGAA[A/G]CTTTTGGCTTCAAGA | 66610 |
rs29435527 | snp | G/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Abi3 | Mm_Celera | 11:95839443 | TCAACCCTGACCTAC[G/T]CTGACCCATCTGCCT | 66610 |
rs29439469 | snp | A/C | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant | Abi3, Phospho1 | GRCm38.p3 | 11:95830189 | GTCTACTCTGCTCTG[A/C]CACCAGAAACCTCCA | 66610 |
rs29439591 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Abi3 | GRCm38.p3 | 11:95835925 | GCCGATCTCCCTTCT[A/G]GCTACCTTCTCCATA | 66610 |
rs29441897 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Abi3, Phospho1 | GRCm38.p3 | 11:95831379 | GGGGATTGGTTAGGA[C/T]CACCTAGTTTTACTA | 66610 |
rs29448317 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime, synonymous-codon | Abi3, Phospho1 | GRCm38.p3 | 11:95830805 | CATCCCCCTGTCGCC[A/G]GGCATGGGCGATTTG | 66610 |
rs29448596 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Gngt2, Abi3 | GRCm38.p3 | 11:95841398 | GGTGGTGGGAGCCTG[C/T]AGTCCCAGCACTGAG | 66610 |
rs29452174 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Abi3 | Mm_Celera | 11:95839890 | ATAGTCTTTGGGGGG[A/C/G]TTTGGGGGGAAGCTG | 66610 |
rs29453837 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Gngt2, Abi3 | GRCm38.p3 | 11:95842371 | CAGGAGAAGGGGGAA[A/G]CCAGGGGCCTGTTGG | 66610 |
rs29457608 | snp | A/G | 0.375 | 0.216506 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | Gngt2, Abi3 | GRCm38.p3 | 11:95842685 | GGCTGGGCTGGCAGT[A/G]CAGCTCCAGTGGTAA | 66610 |
rs29467942 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Abi3 | GRCm38.p3 | 11:95839423 | GACCCTGTTTTTACG[C/T]TCAGTCAACCCTGAC | 66610 |
rs29469742 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Abi3 | Mm_Celera | 11:95839861 | CCACCCCCAAATGGT[A/G]GCACAGGCCTGGAAT | 66610 |
rs29469944 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Abi3, Phospho1 | GRCm38.p3 | 11:95832135 | AATAAAGGAGGTGAA[A/G]GGGGACAAAGGGACT | 66610 |
rs29472672 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Abi3 | GRCm38.p3 | 11:95833090 | AAGATAGGGTCGCCC[C/G]CACCTTGGTAGGGAA | 66610 |
rs29481679 | snp | A/T | 0.375 | 0.216506 | intron-variant | Abi3 | Mm_Celera | 11:95835217 | TCCTGGGGGTCTGGC[A/T]TAGTATCAAGGGGTT | 66610 |
rs29483431 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Abi3 | GRCm38.p3 | 11:95836210 | GAGTCCCATGGCCAT[A/G]CAGCCATTGGAGAAA | 66610 |
rs29483540 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Abi3, Phospho1 | GRCm38.p3 | 11:95831447 | GCATATCTGGAATTC[A/G]GTCTGCTTGTGGGCT | 66610 |
rs45910518 | snp | C/G | | | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | GRCm38.p3 | 11:95843506 | AGAAAGCTAGGAGCT[C/G]TTGGCATGGGGAGGA | 66610 |
rs46266138 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | Mm_Celera | 11:95844378 | AGAATGCTTGCCCAG[C/T]ATCCTCAGTGTCCTG | 66610 |
rs46445165 | snp | C/T | | | utr-variant-3-prime | Abi3, Phospho1 | GRCm38.p3 | 11:95831482 | GCAGGGGTTCAGAGC[C/T]GTCCCTATCTATGCA | 66610 |
rs46861444 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | GRCm38.p3 | 11:95843699 | AGTGTCTGCTGTGGA[C/T]GAGCGGAGGACTGAC | 66610 |
rs46918792 | snp | G/T | | | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | GRCm38.p3 | 11:95842950 | GCTGGAGGCAGCGCT[G/T]GTGAACAGAGCGCTG | 66610 |
rs46943657 | snp | C/T | | | intron-variant | Abi3 | Mm_Celera | 11:95836265 | CTTTGGAGCGACTTC[C/T]GGGTAGAAGAGAATG | 66610 |
rs48024085 | snp | A/G | | | utr-variant-3-prime | Abi3, Phospho1 | GRCm38.p3 | 11:95831529 | TGCCTTCCCTCCAGG[A/G]AGGTGAGCACCCCTT | 66610 |
rs48226904 | snp | C/T | | | upstream-variant-2KB, intron-variant | Gngt2, Abi3 | GRCm38.p3 | 11:95841836 | AGCGTTATACACATA[C/T]CCTCTACCTCTGAGG | 66610 |
rs48257602 | snp | G/T | | | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | GRCm38.p3 | 11:95844415 | ACCCCCCGTAGCATA[G/T]CAACTAGGTACATGC | 66610 |
rs48982789 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | GRCm38.p3 | 11:95842954 | GAGGCAGCGCTGGTG[A/G]ACAGAGCGCTGAGTG | 66610 |
rs48988097 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | GRCm38.p3 | 11:95844224 | GTTGTGAGCCACGAG[A/G]AGGATGCTGGGAATC | 66610 |
rs49095963 | snp | A/G | | | intron-variant | Abi3 | GRCm38.p3 | 11:95835400 | ACAGAGGAAGTCGCT[A/G]TTCTCATGTGGCTGA | 66610 |
rs49374536 | snp | C/T | | | intron-variant, upstream-variant-2KB | Abi3 | GRCm38.p3 | 11:95838257 | TCCCTTGCTTCTCTC[C/T]AGCCACACTAGCTCC | 66610 |
rs49869266 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | GRCm38.p3 | 11:95843784 | GCAGCAGAGATTTGG[C/T]TTTGCCAACCATCTG | 66610 |
rs50060432 | snp | A/G | | | intron-variant, upstream-variant-2KB | Abi3 | GRCm38.p3 | 11:95838181 | GATCAAAGGTGTGTG[A/G]CATCTCCACCCGCCC | 66610 |
rs50238451 | snp | C/G | | | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | GRCm38.p3 | 11:95843587 | TAGGCTAGAGGGAAG[C/G]TGTGGGGCGGGGAGA | 66610 |
rs50368507 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | GRCm38.p3 | 11:95844262 | TATCCTCTGCGAGAG[C/T]AATAAGTGCTCTAAA | 66610 |
rs50380317 | snp | C/T | | | intron-variant, upstream-variant-2KB | Abi3 | GRCm38.p3 | 11:95838328 | TCAGGGCCTTGGCGC[C/T]TACACTTCTTAGAGC | 66610 |
rs50440847 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | Mm_Celera | 11:95843905 | TAACAGGTAAGGAGG[C/T]CTTGGGGCACTGGGC | 66610 |
rs50552157 | snp | A/C | | | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | GRCm38.p3 | 11:95843646 | TGATGGAGTTTGCTC[A/C]GGGGGCCCACAATGG | 66610 |
rs50696512 | snp | C/T | | | intron-variant | Abi3 | Mm_Celera | 11:95835380 | CAATGACCTCAAACC[C/T]CCAGACAGAGGAAGT | 66610 |
rs50910742 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | Abi3, Phospho1 | GRCm38.p3 | 11:95832326 | CTTCTGGGGCAGACT[G/T]CAGGGCTTCCGTGTT | 66610 |
rs50967477 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | Mm_Celera | 11:95843477 | AATGGAAAGCACAGG[A/G]GGCTTCAGGAGGGAG | 66610 |
rs51033990 | snp | C/T | | | intron-variant, upstream-variant-2KB | Abi3, Gngt2 | GRCm38.p3 | 11:95840280 | ATGGAACGGAAAGGC[C/T]TATTTCCATCCCTGC | 66610 |
rs51243833 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gngt2, Abi3 | GRCm38.p3 | 11:95843932 | GGGCTGGGATCTAGT[C/T]TTAGCATGACTCAGT | 66610 |
rs51936780 | snp | C/T | | | intron-variant, upstream-variant-2KB | Abi3 | GRCm38.p3 | 11:95838070 | TACTACTATGTTTTT[C/T]GAGACAGAGTAGCCT | 66610 |
rs52108039 | snp | C/G | | | intron-variant, upstream-variant-2KB | Abi3 | GRCm38.p3 | 11:95838091 | AGAGTAGCCTTGGCT[C/G]TCCTGGAACTCACTC | 66610 |
rs52317580 | snp | A/G | | | intron-variant | Abi3 | Mm_Celera | 11:95836865 | GAGAGAGAGAGAGAG[A/G]GGGAGAGAGAGAGAG | 66610 |
rs52355802 | snp | A/G | | | intron-variant | Abi3 | GRCm38.p3 | 11:95840085 | AAGGAAGGAAGGAAG[A/G]AAGGAAGGAAGGAAG | 66610 |
rs52358950 | snp | A/G | | | intron-variant | Abi3 | GRCm38.p3 | 11:95840090 | AGGAAGGAAGAAAGG[A/G]AGGAAGGAAGAGAGA | 66610 |
rs52414358 | snp | A/G | | | intron-variant | Abi3 | Mm_Celera | 11:95840038 | AGAAAGAGAGAGAGA[A/G]AGAAAGAAAGAAAGA | 66610 |