SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs26969781 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Grap | GRCm38.p3 | 11:61670737 | TTATTAGCGCAGCAC[A/G]GTGTTTTGCTTAGAG | 71520 |
rs26969782 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Grap | GRCm38.p3 | 11:61659620 | ACTTGGTGATGGCAG[C/T]TTCTTCAGCTTGTTT | 71520 |
rs26969783 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Grap | GRCm38.p3 | 11:61658200 | ACTTCTCCTCAGACC[C/T]GTGGCCTCTTTTCAA | 71520 |
rs26969784 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Grap | GRCm38.p3 | 11:61658085 | ATGGTACCATGCACC[C/G]TAGCCGCCTGCCCCT | 71520 |
rs26969785 | snp | C/T | 0.375 | 0.216506 | intron-variant | Grap | GRCm38.p3 | 11:61657227 | GAAAAACTGCACAGA[C/T]AAAAGGGGACATCCT | 71520 |
rs26969786 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Grap | GRCm38.p3 | 11:61656629 | CTGAATGGGCGTGGT[A/G]GAACAGCCACGATCT | 71520 |
rs26969787 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Grap | GRCm38.p3 | 11:61655841 | CTTTGCTTTAAAAAC[A/G]ACTTGCTTTTGAAAA | 71520 |
rs26969788 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Grap | GRCm38.p3 | 11:61655476 | GGAAAGAGGGAGCAC[C/T]GAGTCCAGAAACAGC | 71520 |
rs26969789 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Grap | GRCm38.p3 | 11:61655382 | CCTGGGTGACAGGGG[A/G]TATCCAGCCCAGAGC | 71520 |
rs26969790 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Grap | GRCm38.p3 | 11:61655163 | AGAGTGAAGAATTGT[C/T]CTCAAAAGAGGTGTG | 71520 |
rs26969791 | snp | A/G | 0.375 | 0.216506 | intron-variant | Grap | GRCm38.p3 | 11:61655013 | ATGGGTAGTTGGCAG[A/G]CCTTGGGGTGCAGCT | 71520 |
rs26969792 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Grap | GRCm38.p3 | 11:61654977 | TTTCAGTGAGGGAGC[A/G]GAAGGAAAGCACAAG | 71520 |
rs26969793 | snp | C/T | 0.375 | 0.216506 | intron-variant | Grap | GRCm38.p3 | 11:61654800 | GTACAGTCCCTGGGG[C/T]ACCTACTGTGCAGAG | 71520 |
rs26969794 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Grap | GRCm38.p3 | 11:61654719 | CACTTGAGGCTGGAG[A/G]GTAGCTGGCCTATTA | 71520 |
rs26969795 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Grap | GRCm38.p3 | 11:61654310 | GTGGAAGACCATGGC[C/T]TGGCTGCAGTGAGCG | 71520 |
rs26969796 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Grap | GRCm38.p3 | 11:61653976 | CTCACCTGAGCCACT[C/T]TCACTCACAGTGGTT | 71520 |
rs26969797 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Grap | Mm_Celera | 11:61653880 | AAAATAAGCAGACAT[C/T]CTAACTTAATTGGGC | 71520 |
rs26969798 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Grap | Mm_Celera | 11:61653379 | GTACAGCTTCCAGGC[C/T]ACCGAGAGTGACGAG | 71520 |
rs26969799 | snp | G/T | 0.493827 | 0.0552116 | upstream-variant-2KB | Grap | Mm_Celera | 11:61652580 | TGAGAGGAGACGGTT[G/T]GAAGTGTCTTGAACG | 71520 |
rs26969800 | snp | A/G | 0.489796 | 0.070696 | upstream-variant-2KB | Grap | Mm_Celera | 11:61652338 | CACAGCCTTCCCTTA[A/G]CAATCGCAGAGCTGT | 71520 |
rs26969801 | snp | C/T | 0.336735 | 0.234472 | upstream-variant-2KB | Grap | Mm_Celera | 11:61652194 | CACAGCCTGGGTTCT[C/T]TAGCTGTCCCTGTGT | 71520 |
rs30525608 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Grap | GRCm38.p3 | 11:61662914 | ACACTTTTAATCCAG[A/G]TCTTTGGAACTAGGA | 71520 |
rs45635535 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61654214 | CCACCCTGAGCCCTG[A/G]CTCGAAGATTCAAGC | 71520 |
rs45666083 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656628 | CCTGAATGGGCGTGG[A/T]GGAACAGCCACGATC | 71520 |
rs45700728 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61665040 | GGTCAGGGCCTGGTG[A/G]CATGGCTTAGGACTC | 71520 |
rs45709701 | snp | C/G | | | intron-variant | Grap | Mm_Celera | 11:61663998 | TTGCCTGGCCTGGTA[C/G]GGACAGCAGGGACAG | 71520 |
rs45724140 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655656 | AATAATATATAAAGA[A/G]CTCTTTTGTCTTGTT | 71520 |
rs45865769 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61666457 | GCTCTCTGGAAGACA[A/T]ATTGGTTGGGGACAT | 71520 |
rs45870391 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61669774 | AACTCCAGATTTCCC[C/T]CAGATCAGGGTCTGG | 71520 |
rs45886244 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656383 | CGATTGCCTGGACAG[A/G]ATTGGAAATCCTATC | 71520 |
rs45906989 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61670240 | GAATGTATGTCTGGG[C/T]GCCTGCTGAGTCCCA | 71520 |
rs45962531 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61669670 | AAGGTAAATAAGTTG[C/T]TGGAAGTCACACAGT | 71520 |
rs46001105 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61662151 | AACAAACGAACGAAC[A/G]AACAAACAAACAATG | 71520 |
rs46063044 | snp | G/T | | | intron-variant | Grap | Mm_Celera | 11:61664614 | CTGTTTCCACACAGA[G/T]AAAATAGGTCATTGG | 71520 |
rs46099667 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61666801 | CCCTGAGACCCTTCT[C/T]TCATGGCTGATGGGA | 71520 |
rs46128926 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656590 | GGGGGGTGCACAGAG[C/T]ATGAATTAGATACAG | 71520 |
rs46397891 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61663099 | TGTAGATTTTGGAGC[C/T]ATGTCCAGGCATGGC | 71520 |
rs46421952 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61666558 | TGGTCATCCCTCACC[C/T]GTGATGATGAGGTCA | 71520 |
rs46437353 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Slc5a10, Grap | GRCm38.p3 | 11:61672975 | CTGAGAACTTGAAGC[A/G]CCTGTCTTCCCACTG | 71520 |
rs46471614 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61665570 | AGGATAGCCCAGCCT[C/T]AGTAACTCCTGGAAG | 71520 |
rs46523250 | snp | C/G | | | intron-variant | Grap | Mm_Celera | 11:61663226 | GGGTCAGTAAGCGAG[C/G]GGCTGGCTGGAAAGG | 71520 |
rs46566879 | snp | C/G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61666397 | GGACCTGAAGGGGAG[C/G/T]CCCCTGTTCAGAGGC | 71520 |
rs46708763 | snp | G/T | | | synonymous-codon | Grap | Mm_Celera | 11:61664194 | CCACAGGTGGTACTC[G/T]GGCAGGATCTCTCGA | 71520 |
rs46722868 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61667215 | ACCTGGCAGGGAACT[A/G]TCTCCCCATCGCCCA | 71520 |
rs46786111 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661911 | GTATGCATCATGTTA[C/T]GAAAGTGGGAGGTAG | 71520 |
rs46843192 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61667097 | ATGAGCAGGGCTGGG[C/T]TGCCAGATCCCAGTG | 71520 |
rs46851888 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61663638 | GAGAACTGACTGGTT[A/G]TCCTCTGGTCTACAT | 71520 |
rs46883631 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661959 | ACTATAGCTGCCCAC[C/T]GCCTGCCTAGGTGGG | 71520 |
rs46929606 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61666825 | GATGGGAGATAGATC[C/T]CAATTAAAGTGTCTT | 71520 |
rs47116186 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656312 | TGATCTAAAAAACAA[A/T]TTTTTTTTTTTTTTT | 71520 |
rs47217620 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655704 | ATTTTTCTACATAGG[G/T]TTCCTCCATGTAGCC | 71520 |
rs47230966 | snp | A/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651895 | TAGAAAACCACCGTC[A/T]TGAAAAAAAAAAAAA | 71520 |
rs47320288 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61670577 | TGTGACCCTCAGGGA[C/T]AAGGCCGGGCTGGGC | 71520 |
rs47357905 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61663198 | CTAGCCTAGGACTCA[A/G]TACAATGCCCTGGGG | 71520 |
rs47472803 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670129 | AGGGCAAGGGGGAAA[A/G]ACAGCATAGAAGGTG | 71520 |
rs47480501 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61662007 | TATAGGCTGGGCGGC[A/G]GTGGCACACACCTTT | 71520 |
rs47660284 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655931 | GTGGCAGACAATGAA[G/T]TGACATAATGATCTA | 71520 |
rs47675953 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61665913 | GGGGTCTGAGGGGTG[C/T]CAGGCACGGGAAACA | 71520 |
rs47705489 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61671167 | GCTTCTTCCTTCCTG[A/G]GCTGAGCCCAATAAT | 71520 |
rs47751013 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61663205 | AGGACTCAATACAAT[A/G]CCCTGGGGTCAGTAA | 71520 |
rs47789171 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61658815 | GTTCTCTGGGGAAGG[A/G]GGTCCCACAGCTCCA | 71520 |
rs47858710 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670331 | GGTCTTTCTGTGTGT[C/G]TCTCCCTGGTCTGAA | 71520 |
rs47884472 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656197 | GAATTTAAAAAGCTT[A/T]AAATTTTTGCACTAG | 71520 |
rs47928913 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61670848 | GGGGAGGAGGTTCTC[C/T]GACTTCCCACAATCA | 71520 |
rs48178252 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61663157 | ACCACCACCACCTCC[C/T]AAAGAATCCTTCTAG | 71520 |
rs48181464 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61663098 | ATGTAGATTTTGGAG[C/T]TATGTCCAGGCATGG | 71520 |
rs48422803 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61667847 | GTTGGAAAGTTCTAG[A/G]ACTCCTGGCCCCATG | 71520 |
rs48469719 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661211 | GAGAGAAAAGCATAT[C/T]GTGATGCCTGGGTGC | 71520 |
rs48484106 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670359 | GAAATGCACTGTGTA[A/G]TACAGATGGGCCTTG | 71520 |
rs48503638 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61663797 | CCTGTAACTCCCTCT[C/T]TGGGAGACCTGACAC | 71520 |
rs48506277 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61669827 | GAGGTATTGGGTTTT[C/T]CCCCCCAGTTATGGT | 71520 |
rs48561543 | snp | A/C | | | intron-variant | Grap | Mm_Celera | 11:61665854 | CACTCCGAGACGAGA[A/C]GGGGCAGCAGAGTCC | 71520 |
rs48767457 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61663134 | AGCCTCCCGTTCCTG[A/G]GGACCCCACCACCAC | 71520 |
rs48801068 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61653966 | TTCATTTGTTCTCAC[C/T]TGAGCCACTTTCACT | 71520 |
rs48801573 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656296 | GAGTTTGAGGTCAGC[C/G]TGATCTAAAAAACAA | 71520 |
rs48880665 | snp | C/G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61669572 | GGGAGGGCTCAGAGG[C/G/T]GCCCAGGGACGATGC | 71520 |
rs48896374 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656143 | TGTTTGACTCATAAA[G/T]GGGCTGTAGCCTACA | 71520 |
rs49003432 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61664935 | GAAGGGGATGATGAA[A/G]TTCCATCCATAGCAG | 71520 |
rs49017614 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61654216 | ACCCTGAGCCCTGGC[C/T]CGAAGATTCAAGCAC | 71520 |
rs49152455 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655313 | AGCCCAGAGCCTGGG[A/G]GAGAGGGAGCACCCA | 71520 |
rs49161900 | snp | A/T | | | intron-variant | Grap | Mm_Celera | 11:61663177 | AATCCTTCTAGGCCC[A/T]GCGCTCTAGCCTAGG | 71520 |
rs49195722 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61670895 | CCTCTTTCTTGATAG[C/T]CTGCTATGTAGCCTG | 71520 |
rs49231558 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61664005 | GCCTGGTACGGACAG[C/T]AGGGACAGATTGCCT | 71520 |
rs49236193 | snp | A/T | | | intron-variant | Grap | Mm_Celera | 11:61663581 | CTTCTCACCAAGCCC[A/T]GTGACTTGATTTCAG | 71520 |
rs49279554 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655097 | CATGGGGAGTGAGGC[A/T]GGAGGCTAAGGGTTG | 71520 |
rs49294266 | snp | A/C | | | intron-variant | Grap | Mm_Celera | 11:61665692 | ACTCCTCTTGAGCTC[A/C]CCACAGACCCAGGCT | 71520 |
rs49305099 | snp | C/G | | | intron-variant | Grap | Mm_Celera | 11:61665849 | GGACACACTCCGAGA[C/G]GAGACGGGGCAGCAG | 71520 |
rs49540093 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61667086 | GGCTGGGGAATATGA[A/G]CAGGGCTGGGCTGCC | 71520 |
rs49690780 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656587 | TCTGGGGGGTGCACA[C/G]AGTATGAATTAGATA | 71520 |
rs49752851 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61671082 | GGTTTCTGAGACCCC[A/G]TCTCCCAAACCCCTG | 71520 |
rs49832572 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656013 | CATGTTGTGGTGACC[C/T]CCAACCATGGAATTA | 71520 |
rs49915810 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61669550 | GACACTGAAGAGGTG[G/T]GAGAGAGGGAGGGCT | 71520 |
rs50019586 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670128 | CAGGGCAAGGGGGAA[A/G]AACAGCATAGAAGGT | 71520 |
rs50041782 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61660640 | ACACAGGGACAGGGG[A/G]TCAGAATAGTGGGAT | 71520 |
rs50045600 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61668586 | CTTTCCGACTGGAAG[G/T]CCGAGTGAGATGCTT | 71520 |
rs50111507 | snp | A/G | | | intron-variant, downstream-variant-500B | Slc5a10, Grap | GRCm38.p3 | 11:61673127 | CTAGAGGAGGGTGAA[A/G]TAGGCCAGTGAGGGA | 71520 |
rs50203369 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656299 | TTTGAGGTCAGCCTG[A/G]TCTAAAAAACAATTT | 71520 |
rs50263490 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670807 | TGCTGTGGAGAGGGA[A/G]GGAAGTGTGACTCCA | 71520 |
rs50388019 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61667633 | GCCTCTTTTCCAGAA[C/T]TCAGCTCTTGGGTTT | 71520 |
rs50492435 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61659526 | GCATTGCCAATGCTC[C/T]ATACCAACTATAGGG | 71520 |
rs50512311 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61662972 | TAGATCTTTCCACTT[C/T]GGATTAAGCAAAGCT | 71520 |
rs50554868 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61669563 | TGTGAGAGAGGGAGG[A/G]CTCAGAGGTGCCCAG | 71520 |
rs50642454 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61660697 | AAAGGCAGGCAGCAT[C/T]AGGGTGCCTCTCAGA | 71520 |
rs50657732 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61666319 | AACCTCAGCTTCTCT[A/G]TCCATGAAGTAGGCA | 71520 |
rs50673591 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61661262 | CATGCAGGAGCGAGG[A/G]CTGAGGTCGCCTGGG | 71520 |
rs50771364 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61663255 | GGGCCTTGAGGCCTC[A/G]CTGCAGAAGCTGGCT | 71520 |
rs50870018 | snp | G/T | | | intron-variant | Grap | Mm_Celera | 11:61666057 | CAGCCAACGCACGAT[G/T]CGTAAAGAAACCCTG | 71520 |
rs50927561 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670435 | TGAGCCCGCTACCCT[A/G]CAGTATGAGCACCTC | 71520 |
rs50959590 | snp | C/G | | | intron-variant | Grap | Mm_Celera | 11:61663242 | GGCTGGCTGGAAAGG[C/G]CCTTGAGGCCTCGCT | 71520 |
rs50961680 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670109 | ACAGGAGTTAAGGAC[A/G]GGACAGGGCAAGGGG | 71520 |
rs51025954 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61667311 | CCCCAGTGGACAGAG[C/T]GGTGAGCGCCTAGAT | 71520 |
rs51079189 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61661385 | GGGCTGCAGTCGTCA[A/G]TCAGGCTGTCATGGA | 71520 |
rs51085207 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656242 | TGGTGCATGCCTTTA[A/G]TCCCAGCACTTGGGA | 71520 |
rs51111791 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61662899 | TTAGAGGTCGGGTTA[C/T]CCTAGTTCCAAAGAC | 71520 |
rs51138769 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655551 | GTTTGACTGAAGTGT[A/G]AGAGGGAAGAGAGGA | 71520 |
rs51400160 | snp | C/G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61669483 | CTGTGAGGACTGAGG[C/G/T]GGGAGGGTGATGGGA | 71520 |
rs51529954 | snp | A/T | | | intron-variant | Grap | Mm_Celera | 11:61664760 | ACTGTGCGGTGGCTT[A/T]CTAGGATGAACACGG | 71520 |
rs51555500 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61664416 | GGTTTCTTGGTTAGA[A/G]AGTAGGGGAGGATGC | 71520 |
rs51556965 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61664470 | CCAGAAAGTTCTGCC[A/G]ACAGGGTCCCACTTG | 71520 |
rs51592463 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61664165 | GGATACCTCCAGACA[C/T]GGTCCCCCTCTCCCC | 71520 |
rs51689839 | snp | A/T | | | intron-variant, downstream-variant-500B | Slc5a10, Grap | GRCm38.p3 | 11:61673128 | TAGAGGAGGGTGAAA[A/T]AGGCCAGTGAGGGAT | 71520 |
rs51887136 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670810 | TGTGGAGAGGGAGGG[A/G]AGTGTGACTCCAGCC | 71520 |
rs52014229 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61657412 | TTTTTTTTTAGCATC[A/G]TTTTGAATTTGACCC | 71520 |
rs52059863 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61669779 | CAGATTTCCCTCAGA[A/T]CAGGGTCTGGCTCCA | 71520 |
rs52100540 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61662634 | CTCCTCTCTCGCTCT[C/T]CCTCTCCATCTCTTC | 71520 |
rs52114998 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655296 | GGGGAGAGGGAGCAC[C/T]CAGCCCAGAGCCTGG | 71520 |
rs52121043 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655253 | AACCCAGAGCCTGGG[A/G]GAGAGGGAGCACTCA | 71520 |
rs52147211 | snp | A/T | | | intron-variant | Grap | Mm_Celera | 11:61663893 | ATGAAAATGAATATT[A/T]AAAAAGAAAGATAAT | 71520 |
rs52175933 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656810 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTAAAA | 71520 |
rs52222079 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655344 | GCCCAGAGCCTGGGG[A/G]AGAGGGGGTACCCAG | 71520 |
rs52225710 | snp | A/C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61653806 | GTGTGTGTGTGTGTG[A/C/T]GAGAGAGAGAGAGAG | 71520 |
rs52478760 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655338 | CACCCAGCCCAGAGC[C/T]TGGGGGAGAGGGGGT | 71520 |
rs52487313 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655283 | AGCCCAGAGCCTGGG[A/G]GAGAGGGAGCACCCA | 71520 |
rs107788519 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656806 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 71520 |
rs108267098 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655326 | GGGGAGAGGGAGCAC[C/T]CAGCCCAGAGCCTGG | 71520 |
rs211759785 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61658372 | GTAGTCCAAACAGAC[A/C]TGGAACTCAAAAATC | 71520 |
rs211821571 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61671520 | TACCGGAGCAGCAGA[A/G]GGTCCTTGGCCCCCC | 71520 |
rs211873094 | snp | A/C | | | intron-variant | Grap | Mm_Celera | 11:61665808 | AGAAGTTCCACCATG[A/C]GCAGGTGCGGAAGGA | 71520 |
rs212099973 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61667273 | CCTGTGTGCTGCAGG[A/G]CCAACTTTGCTCTCC | 71520 |
rs212318230 | snp | A/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61653067 | ACTCCATTTAAAACA[A/G]ATAAGAAATGTGAAG | 71520 |
rs212380329 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61660907 | AAGCCATGGGGGTGC[C/T]GGGCCAGGGTGGAGC | 71520 |
rs212492925 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61660494 | TCTTAGGTCTGGGAC[C/G]TAGGTCAGGCTCTTT | 71520 |
rs212728726 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656044 | TTTTTGTTGCTACTC[C/T]ATACCTCCAATTTTG | 71520 |
rs212771111 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61668071 | CTACACCTGAGGGCA[A/G]AGAGGTGGACAGACT | 71520 |
rs212840748 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61671313 | ATGAGCCGATGCCAC[G/T]GCCAGACCCGAGAGC | 71520 |
rs212898391 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61663161 | CCACCACCTCCCAAA[A/G]AATCCTTCTAGGCCC | 71520 |
rs212964599 | in-del | -/A | | | intron-variant | Grap | GRCm38.p3 | 11:61669277 | AGGGAAAAGGAAGGG[-/A]CCATGGTGACAGAGA | 71520 |
rs212985777 | in-del | -/TTT | | | intron-variant | Grap | GRCm38.p3 | 11:61656312 | TGATCTAAAAAACAA[-/TTT]TTTTTTTTTTTTTTT | 71520 |
rs213002470 | in-del | -/G | | | intron-variant | Grap | GRCm38.p3 | 11:61671528 | CAGCAGAGGGTCCTT[-/G]GCCCCCCTCCCCCTC | 71520 |
rs213006568 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61660855 | ATGACCCCTGGCCCT[C/T]TAGTACAGAGGACAG | 71520 |
rs213529793 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61668275 | GCTCAAGGCCAGGTC[A/G]CCTGGTGGTTACAAC | 71520 |
rs213544751 | snp | C/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652496 | TGCCCACCACAATGG[C/T]TCTCCAGCCTGGAGT | 71520 |
rs213602599 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Slc5a10, Grap | GRCm38.p3 | 11:61672725 | TGTGAGCCTGGCATA[C/T]CCTATGCTCCTAACC | 71520 |
rs213687638 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61662359 | GACTCCCTAAGCAGC[C/T]TCTCGGGAGACCTCG | 71520 |
rs213745244 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61661797 | ATTGTAGGGGCAGGG[A/G]GGGCTCCTCAGCAAC | 71520 |
rs213745405 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61669769 | CTTCCAACTCCAGAT[C/T]TCCCTCAGATCAGGG | 71520 |
rs213812557 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61654687 | TGGAAACCAGCATGG[A/G]CCATATCTTTCACAC | 71520 |
rs213852624 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61668891 | GGCATATCTGGGACA[G/T]ATTGTCCCAAAGGGA | 71520 |
rs213915111 | snp | C/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652997 | ATAATCTAAGCCAAA[C/T]AAACCTTTTCCTCCC | 71520 |
rs213949293 | in-del | -/TAG | | | intron-variant | Grap | GRCm38.p3 | 11:61656982 | CTACGTAGCCCAGAC[-/TAG]CTGCAAACCTGCAGT | 71520 |
rs214079536 | snp | A/C | | | intron-variant | Grap | Mm_Celera | 11:61665671 | GAGAGGAACCTGTCC[A/C]GTCCCACTCCTCTTG | 71520 |
rs214091472 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61664866 | AGAGGACTGGTACAC[A/G]GCTTGGGCTTTCTCT | 71520 |
rs214148290 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | Slc5a10, Grap | GRCm38.p3 | 11:61672643 | GTCTTTAAGTCCCTC[A/G]AAGAGCCCAGGTTGC | 71520 |
rs214697634 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655123 | GGTTGGGAGGGCTGC[C/T]TGTAGGTGAAGAAAT | 71520 |
rs214737042 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661625 | CTCTTAGGTGTGAAG[G/T]CTCTGAATGTGGTGG | 71520 |
rs214743653 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656681 | CCTACCCCTCCGAGG[A/G]AGGGCTGGGTGGAGG | 71520 |
rs214767087 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61658171 | CCCTTCCCCTATGGC[C/T]ATGTAGCTAGTGCAC | 71520 |
rs214974462 | in-del | -/ATATAT | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651464 | TATATATGCATGTAC[-/ATATAT]ATATACACATATAGT | 71520 |
rs215012062 | in-del | -/C | | | intron-variant | Grap | GRCm38.p3 | 11:61661049 | TTTTTTTTTTTTCTG[-/C]CTTGTTTCCAAAGCT | 71520 |
rs215028939 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61660463 | GATAGGCTAGAAGTC[C/T]AGTTTGGCCCAGATA | 71520 |
rs215070015 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61670782 | AGATCTGGACATATT[C/T]GAACTTGAGTGCTGT | 71520 |
rs215128033 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61670085 | CAAAGTGACATGAGT[G/T]TGGTTCCTACAGGAG | 71520 |
rs215523411 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61659843 | GCCTCATCAGAACAT[A/G]GGATCTTTTGTTTGT | 71520 |
rs215535860 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61662570 | CACTTCTCGCCTCTG[C/T]TGTAGAGACTGTATT | 71520 |
rs215572630 | snp | G/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652390 | ACAGAAAGCTCAGGT[G/T]GTACTCGATGTTTAA | 71520 |
rs215621800 | snp | A/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651668 | CTCCCAAGTGCTGGG[A/T]TTAAAGGCGTGCGCC | 71520 |
rs215856455 | in-del | -/TA | | | intron-variant | Grap | GRCm38.p3 | 11:61656804 | GTGTGTGTGTGTGTG[-/TA]TGTGTGTGTGTGTGT | 71520 |
rs215921185 | in-del | -/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656574 | GGCAGCTGTCCTTCT[-/G]GGGGGGTGCACAGAG | 71520 |
rs215978252 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61668689 | TGACGCTCTCTCCAG[A/C]CTTTAGACTGGGCTG | 71520 |
rs216001889 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61663121 | AGGCATGGCAGGCAG[C/T]CTCCCGTTCCTGGGG | 71520 |
rs216060746 | in-del | -/GATGCAGGGACCCAA | | | intron-variant | Grap | GRCm38.p3 | 11:61668463 | ATAAGGCTAGATAAG[-/GATGCAGGGACCCAA]GTTGAACCCTGACCC | 71520 |
rs216297617 | snp | G/T | | | intron-variant | Grap | Mm_Celera | 11:61653454 | AGCTGGGCTGAGTGG[G/T]CCAACAGGGTTGGTA | 71520 |
rs216450853 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61659543 | TACCAACTATAGGGG[A/C]TGTGTATGCTGTGCT | 71520 |
rs216679503 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656126 | TGACCCTGTAAAAGG[A/G]TTGTTTGACTCATAA | 71520 |
rs216769061 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661056 | TTTTTTCTGCTTGTT[C/T]CCAAAGCTGCTGCCA | 71520 |
rs216784947 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61668133 | AGTCACTGCAAACAC[C/T]ATGCTGTCAGCTCAT | 71520 |
rs216802888 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61660437 | GCACTGGCTGACTGG[A/T]CTGGGACTTGGATAG | 71520 |
rs217355482 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61671003 | CTCTGTGGTTTCAGA[C/T]CCCAAAAGTGCTCAC | 71520 |
rs217437481 | in-del | -/TTTCTCTCCTC | | | intron-variant | Grap | Mm_Celera | 11:61662611 | TCACACTCTCTCTCA[-/TTTCTCTCCTC]TTTCTCTCTCCTCTC | 71520 |
rs217451894 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655404 | GCCCAGAGCTTGGGA[A/G]AGAGGGAGCAATCAG | 71520 |
rs217503533 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655224 | CAAAGAGCCTTGGGA[A/G]AGACAGAGCACCCAA | 71520 |
rs217532497 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Slc5a10, Grap | GRCm38.p3 | 11:61672495 | TCAGACTTGGCAAGG[C/T]CTGGCATGGTAATGG | 71520 |
rs217615208 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661716 | CTGAGTCCCAGGATG[A/T]TCTCTGTCCCTGGAT | 71520 |
rs217696598 | snp | A/C | | | intron-variant | Grap | Mm_Celera | 11:61663915 | AAAGATAATCTCCAT[A/C]TACAAGCCAGACAGG | 71520 |
rs217713313 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61671470 | AGGTCTCAGAGAGAA[C/T]CAGGCACCTAACCCA | 71520 |
rs217980498 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61657052 | GCATGCACTGAAGCC[C/G]TGCCCTTTTTTCTTG | 71520 |
rs218021510 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61659949 | GGGCCTTCATGTCAT[A/G]TCTCAGTGGTCATTG | 71520 |
rs218026404 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61664752 | GACTGGGGACTGTGC[A/G]GTGGCTTACTAGGAT | 71520 |
rs218032917 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61658750 | CAGGGCCAGTGGTGG[A/G]ACAGACAGGCTCTGA | 71520 |
rs218306272 | snp | C/T | | | utr-variant-3-prime | Grap | GRCm38.p3 | 11:61672202 | CCAACAGCTTGGGGC[C/T]TCCTGGCTTTACCCC | 71520 |
rs218318826 | snp | C/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651840 | GAATCAAAGCCTCTG[C/G]AAGAGTAGCCTGTGC | 71520 |
rs218376176 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61662666 | AGTTAATCTAACAAT[A/G]GCTGGCTATGACCAG | 71520 |
rs218411308 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61666466 | AAGACATATTGGTTG[A/G]GGACATATTGGTAGT | 71520 |
rs218439663 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61669494 | GAGGCGGGAGGGTGA[C/T]GGGAGGCAGGGGAAG | 71520 |
rs218452884 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61665842 | CCACAGAGGACACAC[C/T]CCGAGACGAGACGGG | 71520 |
rs218483137 | in-del | -/CTTT | | | intron-variant | Grap | GRCm38.p3 | 11:61657392 | ATCTTCATTCTGAGA[-/CTTT]TTTTTTTTTTAGCAT | 71520 |
rs218507371 | in-del | -/GTGT | | | intron-variant | Grap | GRCm38.p3 | 11:61656838 | AAATTAGACTTATTA[-/GTGT]GTGTGTGTGTCCCAG | 71520 |
rs218759090 | in-del | -/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656201 | TTAAAAAGCTTAAAA[-/T]TTTTGCACTAGGAGT | 71520 |
rs218833267 | snp | A/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651539 | AGTCATTTTTTAAAA[A/G]TTTTTTTGTTTTTGT | 71520 |
rs218888290 | snp | C/T | | | utr-variant-3-prime | Grap | GRCm38.p3 | 11:61671974 | CAGGCCTGACTGCTT[C/T]CCATTGGTCTCTATG | 71520 |
rs219009682 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61669305 | AGAGGCCAGCAAAGA[C/T]AAGAAGCCAGATCTT | 71520 |
rs219106281 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61665000 | TTTTGGGGGGAGGTA[A/G]CACGAAGCAGGAGGA | 71520 |
rs219170025 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61663381 | ACTCGGGAGGGACAC[A/G]AGGCAGGGAGGGAGG | 71520 |
rs219358908 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61662482 | TCAACTGCCCTTCAA[G/T]CAGGTGAACCCTTCC | 71520 |
rs219452108 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61660691 | ATGTAGAAAGGCAGG[C/T]AGCATCAGGGTGCCT | 71520 |
rs219518487 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61666941 | TTGTCTATACCATCA[A/G]AACGGTGCCACACGG | 71520 |
rs219972484 | in-del | -/CA | | | intron-variant | Grap | GRCm38.p3 | 11:61658492 | ATGTGTGTGTGCGCG[-/CA]CACATGCTTTTCTTG | 71520 |
rs220102738 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61665279 | CCGTTCTGATTGCCC[A/G]TGGAGCTATAAGACC | 71520 |
rs220105062 | snp | A/T | | | intron-variant | Grap | Mm_Celera | 11:61664010 | GTACGGACAGCAGGG[A/T]CAGATTGCCTCAACT | 71520 |
rs220163588 | snp | C/T | | | missense, downstream-variant-500B | Slc5a10, Grap | GRCm38.p3 | 11:61673070 | CGTTGACATTACACA[C/T]GCGGGCCCAGAAAGC | 71520 |
rs220213073 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61666761 | ACCTGTCTGCCTAAC[G/T]TTCCCTTCATATTTC | 71520 |
rs220435597 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61669349 | TGGGTTTTTCATGAA[C/G]GCAATGGCAGCCGTG | 71520 |
rs220442965 | in-del | -/CC | | | intron-variant | Grap | GRCm38.p3 | 11:61657795 | GCATGCTCTCTCTCT[-/CC]CTCCCTCTCTCTCTC | 71520 |
rs220465970 | in-del | -/TCTT | | | intron-variant | Grap | GRCm38.p3 | 11:61666837 | ATCTCAATTAAAGTG[-/TCTT]GCTTCCTTTCTGGCC | 71520 |
rs220469826 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61668466 | AGGCTAGATAAGGAT[A/G]CAGGGACCCAAGTTG | 71520 |
rs220553192 | in-del | -/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652536 | GTGGAATACCCAAAA[-/G]GGTACATGAGGGAGC | 71520 |
rs220593382 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61666082 | ACCCTGGCACACACC[C/T]ACCAGTCCCTTCTCA | 71520 |
rs221274566 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61670960 | AGTTTCCCTTCCATT[C/T]AATGGGTTTGCTTAA | 71520 |
rs221487729 | snp | A/C | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652070 | AAACTAACTAACTAA[A/C]TAAATAAATAATAAA | 71520 |
rs221656473 | in-del | -/GTG | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651499 | CTCTTGAGATTTGTT[-/GTG]TGTGTTTATGAATGT | 71520 |
rs221754543 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655351 | GCCTGGGGGAGAGGG[A/G]GTACCCAGCCCAGAG | 71520 |
rs221992114 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Slc5a10, Grap | GRCm38.p3 | 11:61672820 | TTTGTTTAAAGTGCT[A/G]TTTTTGAAATGATTC | 71520 |
rs222041790 | snp | C/T | | | utr-variant-3-prime | Grap | GRCm38.p3 | 11:61672143 | GGAACTGGCTTAGCC[C/T]TGGGCAACCTCAACG | 71520 |
rs222225683 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61653542 | AGGTTAGCTGCCTCT[A/G]CCCTCTTCAGTTTCC | 71520 |
rs222565487 | snp | C/T | | | utr-variant-3-prime | Grap | GRCm38.p3 | 11:61672091 | TTCCCTTGAGCAGTT[C/T]ATCTTCCAAACGCCT | 71520 |
rs222772603 | snp | C/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652640 | GTGCTTAGGAATCTC[C/G]CTACAGGTATCAGCA | 71520 |
rs222913861 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655713 | CATAGGTTTCCTCCA[C/T]GTAGCCCTGGCTGTC | 71520 |
rs222981724 | snp | C/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652531 | TTGTAGTGGAATACC[C/T]AAAAGGGTACATGAG | 71520 |
rs223219205 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61657602 | ACCAAGTGATGCCAG[C/T]TTGCAGGTGGCACAC | 71520 |
rs223366330 | snp | A/C | | | intron-variant | Grap | Mm_Celera | 11:61665410 | CCATTGGCTACTCCA[A/C]GAGGGTCCCCCACAC | 71520 |
rs223366510 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656623 | GTGAACCTGAATGGG[C/T]GTGGTGGAACAGCCA | 71520 |
rs223429457 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61664736 | CAAAGCAGGGGTGCT[A/G]GACTGGGGACTGTGC | 71520 |
rs223618223 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61657714 | GTGACTCTTAACAGG[A/G]ATGAAGGCCCTCTTT | 71520 |
rs223849716 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61658490 | CATATGTGTGTGTGC[A/G]CGCACATGCTTTTCT | 71520 |
rs224054813 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61661438 | TCAGGATACTCCAGA[A/G]TCAAGGACCCCAAGC | 71520 |
rs224055130 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61654888 | TACTGAGAAAGAGGA[A/G]GGGGTATGCATCATA | 71520 |
rs224447189 | in-del | -/CAGACCTG | | | intron-variant | Grap | GRCm38.p3 | 11:61659347 | TTTTCACTTGCAGAT[-/CAGACCTG]CAGACATGCAGATAT | 71520 |
rs224757668 | snp | G/T | | | intron-variant | Grap | Mm_Celera | 11:61664344 | GTGGGAGCAGGGGGG[G/T]GGGGCAGGCCTGGCA | 71520 |
rs224765890 | in-del | -/CC | | | utr-variant-3-prime | Grap | GRCm38.p3 | 11:61671948 | GGCTGGGAGCGGAAG[-/CC]CCCCCGCCCGCAGGC | 71520 |
rs224831281 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61666806 | AGACCCTTCTCTCAT[A/G]GCTGATGGGAGATAG | 71520 |
rs225029618 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61662985 | TTTGGATTAAGCAAA[A/G]CTCTCTCACAAGTAT | 71520 |
rs225086551 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61662364 | CCTAAGCAGCTTCTC[A/G]GGAGACCTCGGTCCT | 71520 |
rs225111948 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61660038 | TACTTCCTTTCCCCG[A/G]GGCCCCTGGGGGTCT | 71520 |
rs225243408 | snp | A/C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655797 | GCTCCTGCTGTAACC[A/C/G]ACTGTGTTCACCACT | 71520 |
rs225299910 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655385 | GGGTGACAGGGGGTA[C/T]CCAGCCCAGAGCTTG | 71520 |
rs225306298 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61660625 | GTTTCAGGGAGCCAG[A/T]CACAGGGACAGGGGA | 71520 |
rs225506331 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670865 | ACTTCCCACAATCAG[A/G]CTTTGTGTTTTTCTC | 71520 |
rs225581603 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61668494 | TTGAACCCTGACCCC[A/G]ACGAGGGTAGTAATA | 71520 |
rs225581702 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61660864 | GGCCCTTTAGTACAG[A/G]GGACAGGCACTGAGA | 71520 |
rs225644425 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61667983 | GAGCCGGCCCTGCCC[A/C]ACCCCATCCTGCCTT | 71520 |
rs225645175 | snp | C/G | | | synonymous-codon | Grap | GRCm38.p3 | 11:61660275 | TGAGCTCCGAGGAGC[C/G]GAGGGTTTTGTTCCC | 71520 |
rs225867373 | in-del | -/TT | | | intron-variant | Grap | GRCm38.p3 | 11:61657393 | TCTTCATTCTGAGAC[-/TT]TTTTTTTTTTTAGCA | 71520 |
rs225878006 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61662774 | AGAAGCAGGCTCTGA[C/T]GCCAATCAATGAAGG | 71520 |
rs225941660 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61663724 | TTGAGAGTGCATACT[A/G]CTCTTGCAGGGGATC | 71520 |
rs226005421 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61671232 | AGGCCAAGAAGAGCC[C/T]TGTGCTGGGCACTGC | 71520 |
rs226015001 | in-del | -/G | | | utr-variant-3-prime | Grap | GRCm38.p3 | 11:61672127 | GTTGTGCAAGTTACC[-/G]GGAACTGGCTTAGCC | 71520 |
rs226146615 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61665191 | TTGGTCAGTGGCTTT[C/T]CACAACAGCATACTG | 71520 |
rs226226110 | snp | A/C | | | intron-variant | Grap | Mm_Celera | 11:61664442 | GATGCCCAATGAGGC[A/C]CTAGGCTGGTGACCA | 71520 |
rs226250039 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61664381 | CTGGCTGGGTAAAGG[A/G]CTCAGCAAGCAAGTG | 71520 |
rs226274741 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61667772 | GGCAGAAAGGACAAG[A/C]CAAGCCACATACAGC | 71520 |
rs226510656 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61658394 | TCAAAAATCCTCCTG[C/T]TCCAGCTTTCTAAGG | 71520 |
rs226605108 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61667899 | TGGGATCCAAGAACA[C/T]TCCCCTGCAAAACTC | 71520 |
rs226671829 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61667665 | GGGACAGGGTGGAGT[A/C]CTGATGAGCAGTGTG | 71520 |
rs227076007 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61668377 | GCACAGAGAGCTGTT[C/T]GGACCCTGGGGGAAG | 71520 |
rs227378076 | in-del | -/C | | | intron-variant | Grap | GRCm38.p3 | 11:61658276 | TACCTTGGAAACTGT[-/C]CCCCTATCTTTTCAT | 71520 |
rs227393134 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61669650 | AGGAAAGCAGAGGTT[C/T]GGAGAAGGTAAATAA | 71520 |
rs227470335 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61668722 | CAGGGAGCGTCCTCA[A/G]ATTCATCCTAAATCT | 71520 |
rs227485869 | in-del | -/GGGCTCCTGGGGACA | | | intron-variant | Grap | GRCm38.p3 | 11:61671588 | CTCACTTCTCCCACC[-/GGGCTCCTGGGGACA]GGGCTCCTGGGGACA | 71520 |
rs227561687 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Slc5a10, Grap | GRCm38.p3 | 11:61672391 | AGCACTGAGTGAATG[C/T]ACAGTGCATGGGGGT | 71520 |
rs227700577 | snp | A/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651461 | CGTGTATATATGCAT[A/G]TACATATACACATAT | 71520 |
rs227808321 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61667161 | GAAATTTGCTAGTGA[A/G]CTCAAGTGTCCTAGT | 71520 |
rs227810139 | snp | A/G | | | intron-variant, downstream-variant-500B | Slc5a10, Grap | GRCm38.p3 | 11:61673148 | CAGTGAGGGATGAAG[A/G]CTATACTTTCAGTCC | 71520 |
rs227864442 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | Slc5a10, Grap | GRCm38.p3 | 11:61672625 | GAGAGAACCTCTGTG[A/G]CTGTCTTTAAGTCCC | 71520 |
rs228045568 | snp | C/T | | | missense, downstream-variant-500B | Slc5a10, Grap | GRCm38.p3 | 11:61673105 | TTCTGGGGTGTTTGG[C/T]CATCACCTAGAGGAG | 71520 |
rs228057992 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655057 | ATTTGACAAGCACCA[G/T]GCTTAGCCAAGCTTC | 71520 |
rs228161176 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61671423 | TGCCTGGCATCAGTT[A/G]CCGTGTGTATGTGGG | 71520 |
rs228409142 | snp | A/C | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61653000 | ATCTAAGCCAAATAA[A/C]CCTTTTCCTCCCAAG | 71520 |
rs228575405 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655863 | TTTTGAAAACAACAG[A/T]GAAACCTCCAAGGTT | 71520 |
rs228819164 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656454 | GAAACTCCCTTTATA[A/G]CCAGATAGGGCTCTG | 71520 |
rs228857422 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61654075 | CATATGACAGGAGAG[C/T]TGAGGGGGCACAGGA | 71520 |
rs228921433 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61660425 | CCAAGAAGATGGGCA[C/G]TGGCTGACTGGTCTG | 71520 |
rs229121770 | snp | A/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652772 | TGAGAATTGGCTTGT[A/G]GACAAGTCTGTGGGG | 71520 |
rs229173796 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61660744 | GAGATGCTGAGGGAT[A/C]CATGGGAGTTGGCTG | 71520 |
rs229173842 | snp | C/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652350 | TTAACAATCGCAGAG[C/T]TGTAATGCCTTCAGA | 71520 |
rs229922889 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656108 | TTTTTCAATGGTCTT[A/G]GTTGACCCTGTAAAA | 71520 |
rs229932668 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61663831 | CTTCTGGACTCACAT[A/G]CACATACCCCACCCC | 71520 |
rs229932960 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655577 | GAGGACTCTGGGCCT[A/G]TTGGGCAAGCAGAAG | 71520 |
rs230251311 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661700 | CAGCTCCACTCTTTC[C/T]CTGAGTCCCAGGATG | 71520 |
rs230509695 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61668281 | GGCCAGGTCACCTGG[C/T]GGTTACAACCCCCAT | 71520 |
rs230551671 | snp | C/T | | | synonymous-codon | Grap | GRCm38.p3 | 11:61671798 | ACACTGGTGGCGGGG[C/T]CGGGCAGGCGGGCGC | 71520 |
rs230725447 | in-del | -/TTG | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652706 | TGTTTGTTTGGTTTT[-/TTG]TTGTTGTTGTTGTTG | 71520 |
rs230796261 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61661857 | ACAGAAGTTTGCCAG[C/G]GATGTCAGAAACAGG | 71520 |
rs230869573 | in-del | -/TGGAGAACTC | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652242 | CTCTGTGGTTCCATG[-/TGGAGAACTC]TGGTTGCAAATGTAT | 71520 |
rs230977852 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656576 | GCAGCTGTCCTTCTG[A/G]GGGGTGCACAGAGTA | 71520 |
rs231230244 | in-del | -/AGAGTCATCTGGGA | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652741 | AACTTGACACAAGCC[-/AGAGTCATCTGGGA]AGAGGCAGCTTGAGT | 71520 |
rs231342668 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655979 | TTTCCCAGTACTGCG[A/G]CCCTTTAATACAGTT | 71520 |
rs231350264 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61664924 | TGAGGGGTACGGAAG[A/G]GGATGATGAAGTTCC | 71520 |
rs231423326 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61660442 | GGCTGACTGGTCTGG[A/G]ACTTGGATAGGCTAG | 71520 |
rs231436703 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61664023 | GGACAGATTGCCTCA[A/G]CTCTGATTTGCCTCT | 71520 |
rs231439770 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | Slc5a10, Grap | GRCm38.p3 | 11:61672667 | AGGTTGCAGGAACTC[A/G]GGGTTCTCCCTGAGC | 71520 |
rs231661134 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61653991 | TTCACTCACAGTGGT[G/T]GTCTTCCAAGTCATT | 71520 |
rs231699181 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61660482 | TTGGCCCAGATATCT[C/T]AGGTCTGGGACGTAG | 71520 |
rs231709983 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61659894 | TGTCATCCCAAACAC[C/T]AAATATATGTGACCC | 71520 |
rs231711900 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61667257 | GGTCATCCCTGTTCT[C/T]CCTGTGTGCTGCAGG | 71520 |
rs231738906 | snp | A/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652979 | TGGCTTTCCTGATAG[A/T]CTATAATCTAAGCCA | 71520 |
rs231753319 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61660815 | GTGGAAAAAGGGAGG[A/G]AGCCAGAACGAGGCA | 71520 |
rs231769757 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61666703 | ACAGCCAGTTCATTG[A/C]GCAGCTTTCAGAGAG | 71520 |
rs231903908 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655373 | AGCCCAGAGCCTGGG[G/T]GACAGGGGGTATCCA | 71520 |
rs231913817 | snp | A/C | | | intron-variant | Grap | Mm_Celera | 11:61662867 | TTTATATAGGCTTTC[A/C]GTAGGTGTGGCCCAG | 71520 |
rs232069471 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61662577 | CGCCTCTGCTGTAGA[A/G]ACTGTATTAGGGTTC | 71520 |
rs232128295 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61670090 | TGACATGAGTGTGGT[C/T]CCTACAGGAGTTAAG | 71520 |
rs232217264 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61659497 | GAGCCAGTGGGCCAT[A/G]GCCCCTAAGGCCAGC | 71520 |
rs232243336 | in-del | -/CG | | | intron-variant | Grap | Mm_Celera | 11:61653760 | CACAGAGGTAGAAAT[-/CG]TGTGTGTGTGTAAGA | 71520 |
rs232268514 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61658078 | GAAGCTGATGGTACC[A/G]TGCACCCTAGCCGCC | 71520 |
rs232545504 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61662201 | TATAGACCAGCAGAG[A/G]CACAGAGAGACTGGG | 71520 |
rs232691208 | in-del | -/C | | | intron-variant | Grap | GRCm38.p3 | 11:61659867 | GTTTGTCCCCCTATT[-/C]CTAATCCTCACTGTC | 71520 |
rs232979746 | snp | A/C | | | intron-variant | Grap | Mm_Celera | 11:61666267 | AGTCCCAGCTCCCAC[A/C]CCCCCTAGCCTTGAA | 71520 |
rs233001067 | in-del | -/A | | | intron-variant | Grap | Mm_Celera | 11:61664840 | CTCAGAGAGAGGGGG[-/A]ACCATAGGGCAGAGG | 71520 |
rs233221309 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61663552 | CTAGTGAGACGGCTC[A/G]GTGATTAAAGGCACT | 71520 |
rs233478853 | snp | C/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652420 | AAGCACAACAGGGGC[C/T]TTATTAGTGAGGTTT | 71520 |
rs233575956 | snp | C/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651689 | GGCGTGCGCCACCAC[C/T]GCCTAGCCATTTATG | 71520 |
rs233608852 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61666438 | CCCATTGCTCTTGCC[C/T]AGGGCTCTCTGGAAG | 71520 |
rs234089678 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61668145 | CACCATGCTGTCAGC[C/T]CATAAGCAGTTTTGT | 71520 |
rs234109791 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61662058 | AGAGGCAGATGGATG[C/T]CTTGAGTTTGAGGCC | 71520 |
rs234143680 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61670974 | TCAATGGGTTTGCTT[A/T]ACCAGGAGAGATACT | 71520 |
rs234177079 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61667319 | GACAGAGCGGTGAGC[G/T]CCTAGATCTGGCCCA | 71520 |
rs234306747 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61670734 | GGGTTATTAGCGCAG[A/C]ACGGTGTTTTGCTTA | 71520 |
rs234495577 | in-del | -/C | | | intron-variant | Grap | GRCm38.p3 | 11:61661120 | ACACCTGTTCCGGGT[-/C]CCCATCCCTAACCAC | 71520 |
rs234519994 | in-del | -/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652709 | TTTGTTTGGTTTTTT[-/G]TTGTTGTTGTTGTTT | 71520 |
rs234626402 | snp | C/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651715 | TTATGAATGTTTTGA[C/T]GGCATGTGCACATAC | 71520 |
rs234643168 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61667112 | CTGCCAGATCCCAGT[G/T]TGCAGGTAAGGAAAC | 71520 |
rs235262472 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | Slc5a10, Grap | GRCm38.p3 | 11:61672410 | GTGCATGGGGGTGGT[A/G]CCTGGCTATGGGGGA | 71520 |
rs235461138 | snp | A/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61653122 | AGACAGCTCTGCATC[A/G]TCCTAATGGGGACTC | 71520 |
rs235469781 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61660913 | TGGGGGTGCTGGGCC[A/G]GGGTGGAGCTCAGTC | 71520 |
rs235471776 | snp | C/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652556 | CATGAGGGAGCTGTG[C/T]GGAGCAGGTGAGAGG | 71520 |
rs235521148 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61660547 | CTCAGAATGTCTGGA[C/G]AGCTAAACGATCCTT | 71520 |
rs235600088 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61668967 | CCTGAGCATTTTTGA[C/T]GAGAGGCAGCCCCAC | 71520 |
rs235621117 | snp | G/T | | | intron-variant | Grap | Mm_Celera | 11:61662671 | ATCTAACAATGGCTG[G/T]CTATGACCAGAAAGT | 71520 |
rs235631452 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655446 | GGAGAGAGGGAGCAC[C/T]CAGTCCAGAGCCTGG | 71520 |
rs235643159 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655228 | GAGCCTTGGGAAAGA[C/T]AGAGCACCCAACCCA | 71520 |
rs235659290 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61661647 | ATGTGGTGGTGGGGA[A/G]AGAGAGGGGTGTAGC | 71520 |
rs235677956 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61662050 | TGGTAGGTAGAGGCA[A/G]ATGGATGTCTTGAGT | 71520 |
rs235747783 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61654215 | CACCCTGAGCCCTGG[C/T]TCGAAGATTCAAGCA | 71520 |
rs235908455 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656849 | ATTAGTGTGTGTGTG[G/T]GTCCCAGGGATCAAA | 71520 |
rs236048377 | snp | A/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651580 | ACAGGGTTTCTCTGT[A/G]TAGCTCTGGCTGTCC | 71520 |
rs236099498 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61659506 | GGCCATGGCCCCTAA[A/G]GCCAGCATTGCCAAT | 71520 |
rs236109852 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61658373 | TAGTCCAAACAGACC[C/T]GGAACTCAAAAATCC | 71520 |
rs236503695 | snp | A/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651786 | GAGCTTCTAGAGCTG[A/G]AGTTTACAGATGTCT | 71520 |
rs236591255 | in-del | -/G | | | intron-variant | Grap | GRCm38.p3 | 11:61657894 | ACACACACACACACA[-/G]CACACACACGCATAC | 71520 |
rs236852752 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655477 | GAAAGAGGGAGCACT[C/G]AGTCCAGAAACAGCT | 71520 |
rs236855260 | in-del | -/ATGAGTGTGGTT | | | intron-variant | Grap | GRCm38.p3 | 11:61670079 | GGTCACCAAAGTGAC[-/ATGAGTGTGGTT]CCTACAGGAGTTAAG | 71520 |
rs236892299 | snp | A/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652550 | AGGGTACATGAGGGA[A/G]CTGTGTGGAGCAGGT | 71520 |
rs237368022 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Slc5a10, Grap | GRCm38.p3 | 11:61672363 | GTTCAGGAGGAACAG[C/T]CAGGCTATGGCCAGC | 71520 |
rs237369342 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61654689 | GAAACCAGCATGGGC[C/T]ATATCTTTCACACAC | 71520 |
rs237626469 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655798 | CTCCTGCTGTAACCG[A/G]CTGTGTTCACCACTA | 71520 |
rs237638232 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61663397 | AGGCAGGGAGGGAGG[C/T]CACTATTATTGATGT | 71520 |
rs237687484 | snp | A/T | | | intron-variant | Grap | Mm_Celera | 11:61666011 | AAGGGGAGATGGCAG[A/T]GTGCTGGAATAGGTT | 71520 |
rs237747897 | snp | G/T | | | intron-variant | Grap | Mm_Celera | 11:61665329 | TGCTCTAAGGCCACA[G/T]CCCGATGCATCATCA | 71520 |
rs237752652 | snp | C/T | | | utr-variant-3-prime | Grap | GRCm38.p3 | 11:61672002 | ATGTGTGACATCACC[C/T]GCCATTGACCAGGCC | 71520 |
rs237942837 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661717 | TGAGTCCCAGGATGA[C/T]CTCTGTCCCTGGATC | 71520 |
rs237973630 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61658615 | CTTTAAGGCATCCCT[A/G]GGGACAGGCTCCTAG | 71520 |
rs238025706 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61660355 | CCATCCACCTGGAGG[C/T]GATGCGACCCCACCT | 71520 |
rs238037903 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61667000 | CTGGGAGCACCACAG[A/C]ATAGGACAAAGGTCC | 71520 |
rs238089768 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61669464 | GGGCTCAGCCCCCAG[A/G]GTACTGTGAGGACTG | 71520 |
rs238153067 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61668480 | TGCAGGGACCCAAGT[C/T]GAACCCTGACCCCGA | 71520 |
rs238200579 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime | Slc5a10, Grap | GRCm38.p3 | 11:61672299 | AATGTAGTGGGTCCC[C/G]TCCTGTTAGCTACAG | 71520 |
rs238227889 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61654452 | TTGCTTTAATTCTTG[A/G]GCCTTTCTTTGTTCG | 71520 |
rs238343565 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670849 | GGGAGGAGGTTCTCT[A/G]ACTTCCCACAATCAG | 71520 |
rs238787858 | in-del | -/AGACA | | | intron-variant | Grap | GRCm38.p3 | 11:61660194 | AGCAGGTGGCTGAGT[-/AGACA]AGACATATTGTTCCT | 71520 |
rs238910116 | snp | A/G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661271 | GCGAGGACTGAGGTC[A/G/T]CCTGGGTGGCCACAG | 71520 |
rs238937447 | snp | C/G | | | utr-variant-3-prime | Grap | GRCm38.p3 | 11:61672102 | AGTTTATCTTCCAAA[C/G]GCCTTTCAGGTTGTG | 71520 |
rs239013728 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61658454 | TAGCTGGTCCTTTCT[G/T]ATAAATCGGGGCATC | 71520 |
rs239391220 | snp | C/T | | | synonymous-codon | Grap | GRCm38.p3 | 11:61669986 | GATCTTCCTGTGTGA[C/T]GAGCAACCACTGATC | 71520 |
rs239682548 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61662563 | GTGTTCCCACTTCTC[A/G]CCTCTGCTGTAGAGA | 71520 |
rs239747869 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655711 | TACATAGGTTTCCTC[C/T]ATGTAGCCCTGGCTG | 71520 |
rs239759181 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655353 | CTGGGGGAGAGGGGG[C/T]ACCCAGCCCAGAGCC | 71520 |
rs240045395 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61653475 | AGGGTTGGTAGGGTT[A/G]GAACCAGCACCTCAG | 71520 |
rs240103496 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670364 | GCACTGTGTAGTACA[C/G]ATGGGCCTTGAAGTC | 71520 |
rs240117489 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61661183 | CCAGAGACAGGAGGA[A/G]GACACAGGGGAAGAG | 71520 |
rs240140700 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Slc5a10, Grap | GRCm38.p3 | 11:61672965 | GAAGGTGGTCCTGAG[A/G]ACTTGAAGCGCCTGT | 71520 |
rs240483171 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61666775 | CTTTCCCTTCATATT[C/T]CTATCCAGGCCCCTG | 71520 |
rs240494910 | snp | A/C | | | intron-variant | Grap | Mm_Celera | 11:61666270 | CCCAGCTCCCACCCC[A/C]CCTAGCCTTGAAATC | 71520 |
rs240584503 | in-del | -/TGTG | | | intron-variant | Grap | GRCm38.p3 | 11:61656775 | TATTTGCATGTTCTT[-/TGTG]TGTGTGTGTGTGTGT | 71520 |
rs240720074 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61668112 | CACCCTCGGCACCTA[C/T]AGCTTAGTCACTGCA | 71520 |
rs240970952 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656644 | GGAACAGCCACGATC[G/T]GAGCACTGGAGAGGC | 71520 |
rs240987334 | in-del | -/ACAGAC | | | intron-variant | Grap | GRCm38.p3 | 11:61654176 | TGACCCCCTGGAGCA[-/ACAGAC]ACAGGGCTAGATGGC | 71520 |
rs241234164 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61671028 | GCTCACCTGGCTCCA[A/G]TGCCCAGCCTGGTGA | 71520 |
rs241501997 | snp | C/G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61666470 | CATATTGGTTGGGGA[C/G/T]ATATTGGTAGTCTCC | 71520 |
rs241552814 | in-del | -/GC | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651452 | CACGCGTGCGTGTAT[-/GC]ATATGCATGTACATA | 71520 |
rs241659029 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61659954 | TTCATGTCATATCTC[A/C]GTGGTCATTGATTGG | 71520 |
rs241691636 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61658755 | CCAGTGGTGGGACAG[A/G]CAGGCTCTGAGCTTG | 71520 |
rs241924356 | snp | A/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651892 | CTCTAGAAAACCACC[A/G]TCTTGAAAAAAAAAA | 71520 |
rs241940721 | snp | A/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652773 | GAGAATTGGCTTGTG[A/G]ACAAGTCTGTGGGGA | 71520 |
rs241989341 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661922 | GTTACGAAAGTGGGA[G/T]GTAGAAACACCTTCA | 71520 |
rs242006203 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61669316 | AAGACAAGAAGCCAG[A/C]TCTTGAATCTGAAGA | 71520 |
rs242096017 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61654084 | GGAGAGCTGAGGGGG[C/T]ACAGGAGAGTGGCCA | 71520 |
rs242106467 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661613 | GAGGGTCACCCTCTC[C/T]TAGGTGTGAAGGCTC | 71520 |
rs242338457 | snp | C/G | | | intron-variant | Grap | Mm_Celera | 11:61653570 | TCCTCATTTAGGAAA[C/G]TGGAATAGTATTTAT | 71520 |
rs242810545 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61665816 | CACCATGAGCAGGTG[C/T]GGAAGGAAGTCCACA | 71520 |
rs242878253 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655727 | ATGTAGCCCTGGCTG[G/T]CCTGGAACTCACTCT | 71520 |
rs243170841 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61667274 | CTGTGTGCTGCAGGG[C/T]CAACTTTGCTCTCCT | 71520 |
rs243267607 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61657629 | ACACAACTTCCTCTC[C/T]AGGTGCTGCTCAGAA | 71520 |
rs243298077 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61660872 | AGTACAGAGGACAGG[C/T]ACTGAGACAAGGGAG | 71520 |
rs243459400 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61667270 | CTCCCTGTGTGCTGC[A/T]GGGCCAACTTTGCTC | 71520 |
rs243555230 | snp | A/C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61666479 | TGGGGACATATTGGT[A/C/G]GTCTCCTCCTGTCTT | 71520 |
rs243589634 | in-del | -/ACTCT | | | intron-variant | Grap | GRCm38.p3 | 11:61661133 | TCCCCATCCCTAACC[-/ACTCT]ACTCTGCTGGCTTTC | 71520 |
rs243629534 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655174 | TTGTCCTCAAAAGAG[A/G]TGTGGAAATCTGGAG | 71520 |
rs243629640 | snp | C/G | | | intron-variant | Grap | Mm_Celera | 11:61663073 | TAGCCACCACTGAGA[C/G]CAAGTTCCAATGTAG | 71520 |
rs243644219 | in-del | -/C | | | intron-variant | Grap | Mm_Celera | 11:61664951 | TTCCATCCATAGCAG[-/C]CCCCCCCTGCTGGCT | 71520 |
rs243670922 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61663755 | CATGTCTGGTTCCTA[A/G]CACCTACATCTGGCA | 71520 |
rs243688186 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61662379 | GGGAGACCTCGGTCC[C/T]CCCTGGGTTTCAGTT | 71520 |
rs243784391 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61671283 | AGGGAAGACACTGGA[A/G]CCAAAGAGGTAGAGA | 71520 |
rs243842279 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670808 | GCTGTGGAGAGGGAG[C/G]GAAGTGTGACTCCAG | 71520 |
rs243900322 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655398 | TATCCAGCCCAGAGC[C/T]TGGGAAAGAGGGAGC | 71520 |
rs243942768 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61666362 | GAGCTGTGATCTGGA[C/T]GCACACTGCGGCCCA | 71520 |
rs243942781 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61658302 | TTCATCATTGAATTC[C/T]TTTTCTTTTCCTTTT | 71520 |
rs244042051 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61665741 | GGGTGGTCCTGGCTA[A/G]CCACCCTGGGACAGG | 71520 |
rs244051007 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61654940 | CTGAAGGCACAAGGC[A/G]GGAGCAGTGTGCACA | 71520 |
rs244120687 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661963 | TAGCTGCCCACTGCC[C/T]GCCTAGGTGGGAACT | 71520 |
rs244256257 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61659308 | GGGGCTCAGGACTGG[A/G]CTGAGGCACAAGCCT | 71520 |
rs244356661 | in-del | -/A | | | intron-variant | Grap | Mm_Celera | 11:61665484 | GTTCTCTACCCGAGT[-/A]CTGGCCTGGACATCC | 71520 |
rs244371084 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61667905 | CCAAGAACATTCCCC[C/T]GCAAAACTCTCCAAG | 71520 |
rs244740528 | in-del | -/T | | | intron-variant | Grap | GRCm38.p3 | 11:61667755 | GCAGCTATGGGCAAG[-/T]TGGCAGAAAGGACAA | 71520 |
rs245184271 | in-del | -/TTTTTT | | | intron-variant | Grap | GRCm38.p3 | 11:61661007 | GTATTTCCTCTTTGG[-/TTTTTT]TTTTTTTTTTTTTTT | 71520 |
rs245231559 | in-del | -/AGCT | | | intron-variant | Grap | GRCm38.p3 | 11:61655596 | GCAAGCAGAAGAGAC[-/AGCT]ACAGAAGTAGCTCAG | 71520 |
rs245252293 | snp | C/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652650 | ATCTCGCTACAGGTA[C/T]CAGCAGTTGTCCTGC | 71520 |
rs245312101 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61668496 | GAACCCTGACCCCGA[C/T]GAGGGTAGTAATATT | 71520 |
rs245414135 | snp | C/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652575 | GCAGGTGAGAGGAGA[C/T]GGTTGGAAGTGTCTT | 71520 |
rs245427448 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61660628 | TCAGGGAGCCAGACA[C/G]AGGGACAGGGGATCA | 71520 |
rs245444502 | snp | C/T | | | upstream-variant-2KB | Grap | GRCm38.p3 | 11:61651481 | TATACACATATAGTT[C/T]TCTCTCTTGAGATTT | 71520 |
rs245488382 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61667170 | TAGTGAGCTCAAGTG[A/T]CCTAGTGAACCATTT | 71520 |
rs245673758 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | Slc5a10, Grap | GRCm38.p3 | 11:61672548 | gagagagagagagag[A/G]gagagagagagagag | 71520 |
rs245768976 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661745 | ATCTGGAGATGCAGG[C/T]CCTCTATTCTCAGGG | 71520 |
rs245800705 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655081 | AAGCTTCATGCAAGG[G/T]CATGGGGAGTGAGGC | 71520 |
rs245864394 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61668851 | GTCTCTCTGGAGGGC[A/G]CAGCCCTGGGAGCAG | 71520 |
rs245942196 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670059 | TTGCATTCCCCTGCA[A/G]CCCAGGTCACCAAAG | 71520 |
rs246125220 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61662793 | AATCAATGAAGGAAT[A/G]GACTTGCTAGCAAGT | 71520 |
rs246133487 | snp | A/G | | | intron-variant, downstream-variant-500B | Slc5a10, Grap | GRCm38.p3 | 11:61673166 | ATACTTTCAGTCCCC[A/G]TACCTCCAGCCCCAG | 71520 |
rs246169462 | snp | A/G | | | synonymous-codon, downstream-variant-500B | Slc5a10, Grap | GRCm38.p3 | 11:61673071 | GTTGACATTACACAC[A/G]CGGGCCCAGAAAGCA | 71520 |
rs246227628 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Slc5a10, Grap | GRCm38.p3 | 11:61672629 | GAACCTCTGTGGCTG[C/T]CTTTAAGTCCCTCGA | 71520 |
rs246526488 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61661434 | TTCATCAGGATACTC[A/C]AGAGTCAAGGACCCC | 71520 |
rs246542708 | in-del | -/TGAGTA | | | intron-variant | Grap | GRCm38.p3 | 11:61656659 | GAGCACTGGAGAGGC[-/TGAGTA]TGTAGCCCTACCCCT | 71520 |
rs246867247 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61653993 | CACTCACAGTGGTTG[C/T]CTTCCAAGTCATTAG | 71520 |
rs246905062 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656534 | TGAGAAAGCAAACAG[C/T]CAGGCAGACAGGATG | 71520 |
rs246983690 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61654280 | GGTCCCAGGCTCAGT[G/T]TGGATCTCCTGGCTG | 71520 |
rs247446956 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61668385 | AGCTGTTCGGACCCT[C/G]GGGGAAGCTCTGTCT | 71520 |
rs247639033 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61658037 | TGATTAGCTTGCCCC[A/G]GGGACTCAGACTGAT | 71520 |
rs247695708 | in-del | -/TTTTT | | | intron-variant | Grap | GRCm38.p3 | 11:61656311 | TGATCTAAAAAACAA[-/TTTTT]TTTTTTTTTTTTTTT | 71520 |
rs247731089 | snp | A/C/T | | | upstream-variant-2KB | Grap | GRCm38.p3 | 11:61651585 | GTTTCTCTGTATAGC[A/C/T]CTGGCTGTCCTGGAA | 71520 |
rs247852909 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61670313 | AGTTTTGTTTTTAGG[C/T]AGGGTCTTTCTGTGT | 71520 |
rs247954419 | snp | A/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652087 | AAATAAATAATAAAA[A/T]ATAATTTAGAAATAA | 71520 |
rs248036718 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61660116 | TGAGATGCCATAGGT[A/C]CCCATCCAGGGCTCT | 71520 |
rs248239443 | snp | C/G | | | intron-variant | Grap | Mm_Celera | 11:61665475 | GTACAGGAAGGTTCT[C/G]TACCCGAGTCTGGCC | 71520 |
rs248283028 | snp | G/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651499 | TCTCTTGAGATTTGT[G/T]TGTGTTTATGAATGT | 71520 |
rs248590791 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61663222 | CCTGGGGTCAGTAAG[C/T]GAGCGGCTGGCTGGA | 71520 |
rs248966230 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61666753 | TGGCTGGTACCTGTC[C/T]GCCTAACTTTCCCTT | 71520 |
rs249255443 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61660492 | TATCTTAGGTCTGGG[A/T]CGTAGGTCAGGCTCT | 71520 |
rs249287455 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61659942 | CATCTGGGGGCCTTC[A/G]TGTCATATCTCAGTG | 71520 |
rs249453207 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661258 | GGGGCATGCAGGAGC[G/T]AGGACTGAGGTCGCC | 71520 |
rs249505319 | in-del | -/C | | | intron-variant | Grap | Mm_Celera | 11:61653496 | AGCACCTCAGAGAGT[-/C]CTGGGAGTCTGGGCT | 71520 |
rs249553371 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61657505 | CCCTGTGTATGGGCT[C/T]CTTCCTCTCTGGCCA | 71520 |
rs249641438 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61665255 | CCTGTGGACTGCCGT[C/T]CTTCCTCTCCGTTCT | 71520 |
rs249784259 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61654704 | CATATCTTTCACACA[C/T]ACTTGAGGCTGGAGG | 71520 |
rs249788973 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61667795 | CATACAGCCATGACT[A/G]TTACACTGCCCAGCC | 71520 |
rs249792222 | snp | C/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652265 | AAATGTATAGCTGTG[C/T]TTCTCCGTGTTGTGC | 71520 |
rs249802006 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61653628 | AGAGTCTGAGGCCAC[A/G]GAGTCTGGTGGGAGT | 71520 |
rs249802057 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61661905 | GGTGGGGTATGCATC[A/C]TGTTACGAAAGTGGG | 71520 |
rs249905135 | in-del | -/C | | | intron-variant | Grap | GRCm38.p3 | 11:61655347 | AGAGCCTGGGGGAGA[-/C]GGGGGTACCCAGCCC | 71520 |
rs250162153 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61660778 | AGACAAGGGCAATGA[C/T]TTTTGGAATTTTCGG | 71520 |
rs250179009 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656998 | CTGCAAACCTGCAGT[A/G]ATCCTCCCGCCTCAC | 71520 |
rs250241090 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61664933 | CGGAAGGGGATGATG[A/G]AGTTCCATCCATAGC | 71520 |
rs250244128 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61668050 | TAATGACCCCTCCCC[G/T]CACAGCTACACCTGA | 71520 |
rs250547646 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61662128 | ACACAGAGAAATCCT[G/T]TCTCAGAAACAAACG | 71520 |
rs250556710 | in-del | -/G | | | intron-variant | Grap | GRCm38.p3 | 11:61654231 | CGAAGATTCAAGCAC[-/G]GGAGACAGACTCTTT | 71520 |
rs250582969 | in-del | -/TT | | | intron-variant | Grap | GRCm38.p3 | 11:61664054 | CCTATGTGACCTTGA[-/TT]TTTTTTTCCCTATTT | 71520 |
rs250640570 | in-del | -/G | | | intron-variant | Grap | GRCm38.p3 | 11:61671530 | CAGAGGGTCCTTGGC[-/G]CCCCCTCCCCCTCCC | 71520 |
rs250643494 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61669588 | GCCCAGGGACGATGC[C/T]GGCCAATGTTTTTCA | 71520 |
rs250726641 | in-del | -/A | | | intron-variant | Grap | GRCm38.p3 | 11:61656303 | AGGTCAGCCTGATCT[-/A]AAAAACAATTTTTTT | 71520 |
rs251217405 | snp | A/C | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652982 | CTTTCCTGATAGACT[A/C]TAATCTAAGCCAAAT | 71520 |
rs251250281 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61665265 | GCCGTCCTTCCTCTC[C/T]GTTCTGATTGCCCGT | 71520 |
rs251422389 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61664024 | GACAGATTGCCTCAA[C/T]TCTGATTTGCCTCTC | 71520 |
rs251649978 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61666162 | CCCAGCTCAGCCCTG[C/T]GATTGCACTTAGGGC | 71520 |
rs251663927 | in-del | -/A | | | intron-variant | Grap | Mm_Celera | 11:61662855 | TTCCTCCATATCTTT[-/A]TATAGGCTTTCCGTA | 71520 |
rs251849023 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61667510 | AGTGGGGGTTGGGGT[C/T]GGGGTCACAAAGTAC | 71520 |
rs251865005 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655105 | GTGAGGCTGGAGGCT[A/G]AGGGTTGGGAGGGCT | 71520 |
rs251889508 | in-del | -/TTTGTTTTTTT | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651553 | ATTTTTTTGTTTTTG[-/TTTGTTTTTTT]TTTTTTTCAAGACAG | 71520 |
rs251929674 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61664819 | GGCTGAGGGCAGCAG[A/G]GTCACACTCAGAGAG | 71520 |
rs252004827 | in-del | -/TA | | | intron-variant | Grap | GRCm38.p3 | 11:61662082 | GAGGCCAGCCCAGTT[-/TA]TACAGAGCAAATTCT | 71520 |
rs252145724 | snp | C/T | | | utr-variant-3-prime | Grap | GRCm38.p3 | 11:61672157 | CCTGGGCAACCTCAA[C/T]GTCCATAAGAGTGCA | 71520 |
rs252181728 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61658912 | CAAAGAGATGGATGG[A/T]TGCAGAACAGTACAT | 71520 |
rs252200974 | snp | A/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61653059 | CAATAGAAACTCCAT[A/T]TAAAACAGATAAGAA | 71520 |
rs252260936 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61668194 | CACCTCTGGCAGAAC[C/T]TTCCTTTTGGGGGAA | 71520 |
rs252532638 | snp | C/T | | | utr-variant-3-prime | Grap | GRCm38.p3 | 11:61671878 | ACAAGACCAGAGGAG[C/T]GATGCTCTGGGCTCA | 71520 |
rs252625631 | snp | A/G | | | synonymous-codon | Grap | GRCm38.p3 | 11:61671810 | GGGCCGGGCAGGCGG[A/G]CGCCTGGGCTTCTTC | 71520 |
rs252891365 | snp | C/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652565 | GCTGTGTGGAGCAGG[C/T]GAGAGGAGACGGTTG | 71520 |
rs253000137 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61662757 | ACACACTGGAATCCT[A/G]CAGAAGCAGGCTCTG | 71520 |
rs253086992 | in-del | -/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652686 | TGTTTTGTTTGTTTG[-/T]TTTTTTGTTTGTTTG | 71520 |
rs253161098 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656117 | GGTCTTAGTTGACCC[C/T]GTAAAAGGGTTGTTT | 71520 |
rs253325415 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655464 | GTCCAGAGCCTGGGA[A/G]AGAGGGAGCACTGAG | 71520 |
rs253337446 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61663117 | GTCCAGGCATGGCAG[A/G]CAGCCTCCCGTTCCT | 71520 |
rs253464410 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61654854 | TTCCAACAAGCCGGG[C/G]ATCACTTTGCTAAGA | 71520 |
rs253595898 | in-del | -/GGGC | | | intron-variant | Grap | Mm_Celera | 11:61664338 | AGTGGGTGGGAGCAG[-/GGGC]GGGGGTGGGGCAGGC | 71520 |
rs253663026 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61660428 | AGAAGATGGGCACTG[A/G]CTGACTGGTCTGGGA | 71520 |
rs253718075 | in-del | -/AGAGAC | | | intron-variant | Grap | Mm_Celera | 11:61653846 | GACAGAGAGAGACAG[-/AGAGAC]AGAGAGAGAGTCTAA | 71520 |
rs253718294 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61667141 | ACCAACACTCTGAGT[A/G]GCGAGAAATTTGCTA | 71520 |
rs253818692 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670919 | TAGCCTGGGGGAGGG[A/G]TCATTTCAACCCTTA | 71520 |
rs254142284 | in-del | -/CGCGTG | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651440 | ACATACACACACACA[-/CGCGTG]CGTGTATATATGCAT | 71520 |
rs254148990 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61658378 | CAAACAGACCTGGAA[C/T]TCAAAAATCCTCCTG | 71520 |
rs254159744 | snp | A/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651521 | TATGAATGTTTTTTT[A/T]AAAGTCATTTTTTAA | 71520 |
rs254188575 | in-del | -/A | | | intron-variant | Grap | GRCm38.p3 | 11:61662168 | CAAACAAACAATGAC[-/A]AAACCCATCCATCAC | 71520 |
rs254289159 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61668649 | TTCTGGGGTTACAAA[C/T]CCTGCTGGGGCTACA | 71520 |
rs254353323 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61671453 | GCCCAGAGGGAGGGA[A/G]TAGGTCTCAGAGAGA | 71520 |
rs254671186 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61658677 | GTCTGTACCCAGTAG[A/G]TGCTCAAGCAAGCTG | 71520 |
rs254765800 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61657667 | GTGGAAACCCCCTAG[A/G]CCATAGGCTTTCTCA | 71520 |
rs254816069 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61665333 | CTAAGGCCACAGCCC[A/G]ATGCATCATCATGTG | 71520 |
rs254828590 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61661253 | GGGCTGGGGCATGCA[A/G]GAGCGAGGACTGAGG | 71520 |
rs254943170 | in-del | -/TGG | | | intron-variant | Grap | GRCm38.p3 | 11:61659811 | TAAGTATCTGGGAAC[-/TGG]GACTCTCAGAACTGG | 71520 |
rs255017781 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61662006 | TTATAGGCTGGGCGG[C/T]GGTGGCACACACCTT | 71520 |
rs255082559 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61661435 | TCATCAGGATACTCC[A/G]GAGTCAAGGACCCCA | 71520 |
rs255168015 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61668487 | ACCCAAGTTGAACCC[C/T]GACCCCGACGAGGGT | 71520 |
rs255187932 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61660863 | TGGCCCTTTAGTACA[A/G]AGGACAGGCACTGAG | 71520 |
rs255457570 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61668284 | CAGGTCACCTGGTGG[C/T]TACAACCCCCATGGA | 71520 |
rs255493938 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61657282 | GCTAGCCATGGTCCC[A/G]GTGAACTGGTTTGAT | 71520 |
rs255888498 | snp | A/C | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652762 | CAGCTTGAGTTGAGA[A/C]TTGGCTTGTGGACAA | 71520 |
rs255988888 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61660724 | CAGAAAAGGTGGCAA[G/T]GAGTGAGATGCTGAG | 71520 |
rs255992346 | snp | C/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652437 | TATTAGTGAGGTTTT[C/G]ATAGGTGAATAGGAG | 71520 |
rs256007210 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61660449 | TGGTCTGGGACTTGG[A/C]TAGGCTAGAAGTCTA | 71520 |
rs256050018 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61660409 | TGGGGTACAATACAC[C/T]CCAAGAAGATGGGCA | 71520 |
rs256523411 | snp | A/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652567 | TGTGTGGAGCAGGTG[A/G]GAGGAGACGGTTGGA | 71520 |
rs256525867 | snp | A/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652534 | TAGTGGAATACCCAA[A/G]AGGGTACATGAGGGA | 71520 |
rs256587326 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61667975 | GGAGTCCGGAGCCGG[C/T]CCTGCCCCACCCCAT | 71520 |
rs256639046 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655376 | CCAGAGCCTGGGTGA[C/G]AGGGGGTATCCAGCC | 71520 |
rs257074389 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61671224 | CTCAGCAGAGGCCAA[A/G]AAGAGCCCTGTGCTG | 71520 |
rs257172724 | in-del | -/GT | | | intron-variant | Grap | Mm_Celera | 11:61653761 | ACAGAGGTAGAAATC[-/GT]GTGTGTGTGTAAGAG | 71520 |
rs257222552 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61658122 | TTCCAGCTCTGGACT[C/T]CTGTCTGGAATCTGA | 71520 |
rs257235931 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61665627 | CCAAACAGGGGCACC[C/T]GGCACAGATCAGGCC | 71520 |
rs257302932 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime | Slc5a10, Grap | GRCm38.p3 | 11:61672713 | GACCCTCTAAGCTGT[C/G]AGCCTGGCATACCCT | 71520 |
rs257576801 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670427 | GGCTGGGGTGAGCCC[A/G]CTACCCTGCAGTATG | 71520 |
rs257591997 | in-del | -/TACT | | | intron-variant | Grap | Mm_Celera | 11:61665310 | ACACCAGGCTGGGGC[-/TACT]TACTGCTCTAAGGCC | 71520 |
rs257648631 | snp | A/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651690 | GCGTGCGCCACCACC[A/G]CCTAGCCATTTATGA | 71520 |
rs257668369 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670995 | GAGAGATACTCTGTG[A/G]TTTCAGACCCCAAAA | 71520 |
rs257902150 | snp | C/G | | | intron-variant | Grap | Mm_Celera | 11:61663325 | GGCCTTGCAAGAGTC[C/G]CAAGACCTAGCGGGT | 71520 |
rs257902678 | snp | A/T | | | intron-variant | Grap | Mm_Celera | 11:61653521 | TGGGCTGTGAGGGAC[A/T]GGCTCAGGTTAGCTG | 71520 |
rs257920556 | in-del | -/CAT | | | intron-variant | Grap | GRCm38.p3 | 11:61657335 | TCCACACTTCCTATG[-/CAT]CATTTCAATTTGTTA | 71520 |
rs258016173 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661210 | AGAGAGAAAAGCATA[G/T]CGTGATGCCTGGGTG | 71520 |
rs258027905 | snp | A/G | | | intron-variant, downstream-variant-500B | Slc5a10, Grap | GRCm38.p3 | 11:61673200 | GAGGAAGGATGAGGA[A/G]CGATTGCTGGGTTAC | 71520 |
rs258230016 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61666876 | TGCCTTGGAGTTATA[A/G]CACACACTTGTCTAT | 71520 |
rs258332903 | snp | C/G | | | intron-variant | Grap | Mm_Celera | 11:61666280 | ACCCCCCCTAGCCTT[C/G]AAATCCAGGCACGTT | 71520 |
rs258388990 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655913 | CTGTGTCTTCCCGTT[A/G]GGGTGGCAGACAATG | 71520 |
rs258395458 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61662240 | CCAGGATCACTTAGC[C/T]TGCAAGAAGTAGACT | 71520 |
rs258403195 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655712 | ACATAGGTTTCCTCC[A/G]TGTAGCCCTGGCTGT | 71520 |
rs258543224 | in-del | -/TG | | | intron-variant | Grap | Mm_Celera | 11:61665345 | CCCGATGCATCATCA[-/TG]TGTTCTGTCTCCTGC | 71520 |
rs258551261 | in-del | -/CTCTCTCTCTCT | | | intron-variant | Grap | GRCm38.p3 | 11:61657923 | CACACACACACACAG[-/CTCTCTCTCTCT]CTCTCTCTCACACAC | 71520 |
rs258592168 | in-del | -/G | | | intron-variant | Grap | GRCm38.p3 | 11:61671136 | GGTCACCCATTGGCA[-/G]GGGGGCAGGGTGAGA | 71520 |
rs258624324 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656645 | GAACAGCCACGATCT[A/G]AGCACTGGAGAGGCT | 71520 |
rs258789042 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61658063 | CTGATATCTCCCTGG[A/G]AAGCTGATGGTACCA | 71520 |
rs258881932 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61659710 | GCTTTCCACCCTTCA[A/G]TGGTTCACCCAGTGA | 71520 |
rs259072504 | in-del | -/TCAAGCAGGG | | | intron-variant | Grap | GRCm38.p3 | 11:61661495 | CTGCCTATGCTTGGA[-/TCAAGCAGGG]TCATGATCAGGTTCT | 71520 |
rs259178820 | snp | C/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651446 | ACACACACACGCGTG[C/T]GTGTATATATGCATG | 71520 |
rs259228545 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61668114 | CCCTCGGCACCTACA[A/G]CTTAGTCACTGCAAA | 71520 |
rs259267224 | in-del | -/A | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652083 | AACTAAATAAATAAT[-/A]AAAAATAATTTAGAA | 71520 |
rs259421300 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61661944 | ACACCTTCAGCTGTT[A/C]CTATAGCTGCCCACT | 71520 |
rs259487520 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61669335 | TGAATCTGAAGAGCT[G/T]GGTTTTTCATGAAGG | 71520 |
rs259504131 | snp | A/G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655343 | AGCCCAGAGCCTGGG[A/G/T]GAGAGGGGGTACCCA | 71520 |
rs259620577 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655015 | GGGTAGTTGGCAGGC[C/T]TTGGGGTGCAGCTTC | 71520 |
rs259672486 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61660925 | GCCAGGGTGGAGCTC[A/T]GTCAGCAGGTGGAAG | 71520 |
rs259680933 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61662057 | TAGAGGCAGATGGAT[G/T]TCTTGAGTTTGAGGC | 71520 |
rs259941106 | snp | C/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652800 | GGGACGTTTTCCTGA[C/T]TAATGACTGGTGTGG | 71520 |
rs260012825 | in-del | -/A | | | intron-variant | Grap | GRCm38.p3 | 11:61670805 | GTGCTGTGGAGAGGG[-/A]AGGGAAGTGTGACTC | 71520 |
rs260157783 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61664737 | AAAGCAGGGGTGCTG[A/G]ACTGGGGACTGTGCG | 71520 |
rs260306809 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61660592 | TATTCTTTAAATGGC[A/G]TCTGGGTCATTGATC | 71520 |
rs260315075 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61669595 | GACGATGCCGGCCAA[A/T]GTTTTTCAGCTTTCT | 71520 |
rs260394982 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61667293 | CTTTGCTCTCCTTTT[C/G]TTCCCCAGTGGACAG | 71520 |
rs260453843 | in-del | -/TGTG | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651495 | CTCTCTCTTGAGATT[-/TGTG]TGTTTGTGTTTATGA | 71520 |
rs260473442 | in-del | -/G | | | intron-variant | Grap | GRCm38.p3 | 11:61660681 | CAGAAAGTATATGTA[-/G]AAAGGCAGGCAGCAT | 71520 |
rs260670081 | in-del | -/GGATA | | | intron-variant | Grap | GRCm38.p3 | 11:61657185 | GTGTTGACTGTAACT[-/GGATA]GGCTTTAGACCTGTT | 71520 |
rs260747902 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61670149 | CATAGAAGGTGGGGG[A/C]AGTTCAGAAACTCCA | 71520 |
rs260765571 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61669040 | GGGCCTCAGTTTCCC[C/T]ACTGTGCATTAGGCC | 71520 |
rs260888060 | in-del | -/GTGT | | | intron-variant | Grap | GRCm38.p3 | 11:61662925 | AGACCTGGATTAAAA[-/GTGT]GTCTTCCTGCCTCAG | 71520 |
rs261076568 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61665839 | AGTCCACAGAGGACA[C/T]ACTCCGAGACGAGAC | 71520 |
rs261514492 | in-del | -/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652702 | TTTTTGTTTGTTTGG[-/T]TTTTTTGTTGTTGTT | 71520 |
rs261548055 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656453 | AGAAACTCCCTTTAT[A/G]GCCAGATAGGGCTCT | 71520 |
rs261596401 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655815 | TGTGTTCACCACTAT[G/T]TCCAGCACCACTTTG | 71520 |
rs261690371 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61668501 | CTGACCCCGACGAGG[A/G]TAGTAATATTGGCTC | 71520 |
rs261695511 | in-del | -/CT | | | intron-variant | Grap | GRCm38.p3 | 11:61654631 | ACCTGGGGTGGGAGA[-/CT]CTGTCCAGATCCAAG | 71520 |
rs261765860 | snp | A/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651804 | TTTACAGATGTCTGC[A/G]AGCCACTATGTAGGG | 71520 |
rs261861121 | snp | A/G | | | missense, downstream-variant-500B | Slc5a10, Grap | GRCm38.p3 | 11:61673088 | GGGCCCAGAAAGCAC[A/G]TTTCTGGGGTGTTTG | 71520 |
rs261923034 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655544 | TTGAAGAGTTTGACT[G/T]AAGTGTAAGAGGGAA | 71520 |
rs262139134 | in-del | -/AGAG | | | intron-variant | Grap | Mm_Celera | 11:61653738 | AACACAGAGAGAAAC[-/AGAG]AGACACAGAGGTAGA | 71520 |
rs262180937 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61654014 | AAGTCATTAGACACA[C/T]GAGTGTGTGAAATCT | 71520 |
rs262663174 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61654466 | GAGCCTTTCTTTGTT[C/T]GGTCCCCTGGGTGTC | 71520 |
rs262691765 | snp | C/T | | | synonymous-codon | Grap | GRCm38.p3 | 11:61660260 | GAACTGGTACAAAGC[C/T]GAGCTCCGAGGAGCG | 71520 |
rs262880660 | snp | A/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652180 | TCTGGTACCCATCCC[A/T]CAGCCTGGGTTCTTT | 71520 |
rs262947257 | in-del | -/G | | | intron-variant | Grap | GRCm38.p3 | 11:61663370 | AGTCTGCTCCTACTC[-/G]GGAGGGACACAAGGC | 71520 |
rs263098385 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61658459 | GGTCCTTTCTTATAA[A/T]TCGGGGCATCTCCCA | 71520 |
rs263141914 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61668417 | CTCATTCTGGTGCCT[A/G]TATGCAAAGCCTTTG | 71520 |
rs263258233 | snp | G/T | | | intron-variant | Grap | Mm_Celera | 11:61662569 | CCACTTCTCGCCTCT[G/T]CTGTAGAGACTGTAT | 71520 |
rs263321426 | snp | A/G | | | utr-variant-3-prime | Grap | GRCm38.p3 | 11:61672015 | CCCGCCATTGACCAG[A/G]CCCATCCTCTCCAGA | 71520 |
rs263379308 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61657567 | CCCCTGGTGGGCTCT[G/T]GTGGGTGTAACTATG | 71520 |
rs263384827 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61660808 | GGGGAAAGTGGAAAA[A/G]GGGAGGAAGCCAGAA | 71520 |
rs263463799 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655229 | AGCCTTGGGAAAGAC[A/G]GAGCACCCAACCCAG | 71520 |
rs263746930 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655087 | CATGCAAGGGCATGG[A/G]GAGTGAGGCTGGAGG | 71520 |
rs263749344 | in-del | -/GA | | | downstream-variant-500B, utr-variant-3-prime | Slc5a10, Grap | GRCm38.p3 | 11:61672529 | TTGATGTGGGGGTGG[-/GA]GAGAGAGAGAGAGAG | 71520 |
rs263841084 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61659987 | ACTCTGTGTTCCTGC[A/G]AACATAGCTCAGTCA | 71520 |
rs263936653 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61666266 | GAGTCCCAGCTCCCA[C/T]CCCCCCTAGCCTTGA | 71520 |
rs264111903 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime | Slc5a10, Grap | GRCm38.p3 | 11:61672380 | AGGCTATGGCCAGCA[C/G]TGAGTGAATGTACAG | 71520 |
rs264132953 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61658759 | TGGTGGGACAGACAG[A/G]CTCTGAGCTTGACCT | 71520 |
rs264220203 | in-del | -/AACC | | | intron-variant | Grap | Mm_Celera | 11:61665381 | CTTAGCAGCCACCGT[-/AACC]AACCATGCAGCAGCC | 71520 |
rs264233351 | in-del | -/GGGGCG | | | intron-variant | Grap | GRCm38.p3 | 11:61664337 | GAGTGGGTGGGAGCA[-/GGGGCG]GGGGGGTGGGGCAGG | 71520 |
rs264419021 | snp | A/G | | | intron-variant | Grap | Mm_Celera | 11:61665186 | GACCTTTGGTCAGTG[A/G]CTTTCCACAACAGCA | 71520 |
rs264453480 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | Slc5a10, Grap | GRCm38.p3 | 11:61672808 | CCCATATCTGACTTT[G/T]TTTAAAGTGCTATTT | 71520 |
rs264525377 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61670678 | CATCAGGGAGCCAGG[A/G]GCAGCTCTCACTCTC | 71520 |
rs264657836 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61667754 | GGGCAGCTATGGGCA[A/G]GTGGCAGAAAGGACA | 71520 |
rs265075968 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61654963 | TGTGCACAGTCGGCT[G/T]TCAGTGAGGGAGCGG | 71520 |
rs265137457 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655734 | CCTGGCTGTCCTGGA[A/G]CTCACTCTGCAGCCC | 71520 |
rs265174384 | snp | A/G | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61652354 | CAATCGCAGAGCTGT[A/G]ATGCCTTCAGACCAC | 71520 |
rs265239095 | snp | G/T | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651495 | TCTCTCTCTTGAGAT[G/T]TGTTTGTGTTTATGA | 71520 |
rs265256355 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61659084 | GAGACAACAGAAGTA[A/G]CCAGAGCTCAAAAGC | 71520 |
rs265402335 | in-del | -/AG | | | intron-variant | Grap | GRCm38.p3 | 11:61656837 | AAAATTAGACTTATT[-/AG]TGTGTGTGTGTGTCC | 71520 |
rs265446165 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61659146 | CACATTGGGGAAATT[A/G]TTTCATTTAGAGTGA | 71520 |
rs265455312 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655356 | GGGGAGAGGGGGTAC[C/T]CAGCCCAGAGCCTGG | 71520 |
rs265510966 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656539 | AAGCAAACAGCCAGG[C/T]AGACAGGATGGGCTC | 71520 |
rs265527425 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61664431 | GAGTAGGGGAGGATG[C/T]CCAATGAGGCCCTAG | 71520 |
rs265546079 | in-del | -/AAAA | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651898 | AAAACCACCGTCTTG[-/AAAA]AAAAAAAAAAATCTG | 71520 |
rs265662944 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61667157 | GCGAGAAATTTGCTA[C/G]TGAGCTCAAGTGTCC | 71520 |
rs265718896 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661380 | TGCAAGGGCTGCAGT[C/T]GTCAATCAGGCTGTC | 71520 |
rs265773841 | snp | A/C | | | intron-variant | Grap | Mm_Celera | 11:61662837 | GCAGAGAGCCAAGCC[A/C]TCTTCCTCCATATCT | 71520 |
rs265808289 | snp | A/G | | | downstream-variant-500B | Slc5a10, Grap | GRCm38.p3 | 11:61672780 | CATTAACCAGTGGAC[A/G]TCAATCTTTCTCCCC | 71520 |
rs265895865 | snp | C/G | | | intron-variant | Grap | Mm_Celera | 11:61665493 | CCCGAGTCTGGCCTG[C/G]ACATCCCTTAACTCC | 71520 |
rs266042032 | in-del | -/TGT | | | intron-variant | Grap | GRCm38.p3 | 11:61656357 | AGATGGCACTCTTGA[-/TGT]TGTTGAAGCGATTGC | 71520 |
rs266147785 | snp | C/T | | | intron-variant | Grap | Mm_Celera | 11:61663441 | TTGTGGTGCCGAGGA[C/T]GAACGTGGAGTGTCG | 71520 |
rs266165256 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61671081 | TGGTTTCTGAGACCC[C/T]ATCTCCCAAACCCCT | 71520 |
rs386886834 | in-del | -/TT | | | intron-variant | Grap | GRCm38.p3 | 11:61657404 | AGACTTTTTTTTTTT[-/TT]AGCATCGTTTTGAAT | 71520 |
rs386908549 | snp | C/T | | | upstream-variant-2KB | Grap | GRCm38.p3 | 11:61651428 | ACACACACACACACA[C/T]ACACACACACACGCG | 71520 |
rs386960890 | in-del | -/TCTCTCTCTCTC | | | intron-variant | Grap | GRCm38.p3 | 11:61657932 | ACACAGCTCTCTCTC[-/TCTCTCTCTCTC]ACACACACACACATG | 71520 |
rs386988625 | in-del | -/G | | | intron-variant | Grap | Mm_Celera | 11:61663372 | TCTGCTCCTACTCGG[-/G]AGGGACACAAGGCAG | 71520 |
rs387046321 | in-del | -/C | | | intron-variant | Grap | Mm_Celera | 11:61664958 | CATAGCAGCCCCCCC[-/C]TGCTGGCTGTGAGGA | 71520 |
rs387089560 | in-del | -/ATGTGT | | | intron-variant | Grap | GRCm38.p3 | 11:61656819 | TGTGTGTGTGTGTGT[-/ATGTGT]GTAAAATTAGACTTA | 71520 |
rs387172568 | in-del | -/GA | | | intron-variant | Grap | Mm_Celera | 11:61653831 | AGAGAGAGAGAGAGA[-/GA]CAGAGAGAGACAGAG | 71520 |
rs387269406 | in-del | -/TT | | | intron-variant | Grap | Mm_Celera | 11:61664061 | GACCTTGATTTTTTT[-/TT]CCCTATTTCTCAATT | 71520 |
rs387306057 | in-del | -/CC | | | intron-variant | Grap | GRCm38.p3 | 11:61657796 | CATGCTCTCTCTCTC[-/CC]TCCCTCTCTCTCTCT | 71520 |
rs387321500 | in-del | -/C | | | intron-variant | Grap | GRCm38.p3 | 11:61661050 | TTTTTTTTTTTCTGC[-/C]TTGTTTCCAAAGCTG | 71520 |
rs387374084 | in-del | -/GTTTTTTTTTT | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651556 | TTTTTGTTTTTGTTT[-/GTTTTTTTTTT]TTTTCAAGACAGGGT | 71520 |
rs387410069 | in-del | -/CA | | | intron-variant | Grap | GRCm38.p3 | 11:61666470 | CATATTGGTTGGGGA[-/CA]TATTGGTAGTCTCCT | 71520 |
rs387521128 | in-del | -/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656205 | AAAGCTTAAAATTTT[-/T]GCACTAGGAGTCAGG | 71520 |
rs387549755 | in-del | -/GTGT | | | intron-variant | Grap | GRCm38.p3 | 11:61656848 | TATTAGTGTGTGTGT[-/GTGT]CCCAGGGATCAAACC | 71520 |
rs387577460 | in-del | -/GTGTA | | | intron-variant | Grap | GRCm38.p3 | 11:61654350 | AAGGTGTCTGTACGT[-/GTGTA]GTGTAGTGTAGTGTA | 71520 |
rs387586998 | in-del | -/ACACAC | | | intron-variant | Grap | GRCm38.p3 | 11:61657848 | CACACACACACACAC[-/ACACAC]GCATACACACAGCTC | 71520 |
rs387714236 | in-del | -/AAAA | | | upstream-variant-2KB | Grap | Mm_Celera | 11:61651909 | CTTGAAAAAAAAAAA[-/AAAA]TCTGCCAGGCAGTGG | 71520 |
rs387776055 | in-del | -/CGGG | | | intron-variant | Grap | Mm_Celera | 11:61664341 | GGGTGGGAGCAGGGG[-/CGGG]GGTGGGGCAGGCCTG | 71520 |
rs387803730 | in-del | -/G | | | intron-variant | Grap | Mm_Celera | 11:61663371 | GTCTGCTCCTACTCG[-/G]GAGGGACACAAGGCA | 71520 |
rs387807874 | in-del | -/G | | | intron-variant | Grap | GRCm38.p3 | 11:61671141 | CCCATTGGCAGGGGG[-/G]CAGGGTGAGAGCTTC | 71520 |
rs387832318 | in-del | -/GTGT | | | intron-variant | Grap | Mm_Celera | 11:61662927 | ACCTGGATTAAAAGT[-/GTGT]CTTCCTGCCTCAGAG | 71520 |
rs387875796 | in-del | -/GAGCCC | | | intron-variant | Grap | GRCm38.p3 | 11:61666477 | TTGGGGACATATTGG[-/GAGCCC]TAGTCTCCTCCTGTC | 71520 |
rs387899320 | in-del | -/AT | | | intron-variant | Grap | GRCm38.p3 | 11:61656809 | TGTGTGTGTGTGTGT[-/AT]GTGTGTGTGTGTAAA | 71520 |
rs578410855 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655441 | GCCTGGGAGAGAGGG[A/G]GCACCCAGTCCAGAG | 71520 |
rs578650619 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655420 | AGAGGGAGCAATCAG[C/T]CCAGAGCCTGGGAGA | 71520 |
rs578815706 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61659794 | AGGGTATCTGTGGGG[C/T]CTAAGTATCTGGGAA | 71520 |
rs578859915 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61653802 | GTGTGTGTGTGTGTG[A/T]GTGAGAGAGAGAGAG | 71520 |
rs579028320 | snp | C/T | | | upstream-variant-2KB | Grap | GRCm38.p3 | 11:61652226 | TTTGGAGAATACTGG[C/T]TCTCTGTGGTTCCAT | 71520 |
rs579031328 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61664322 | AGTGAGCTCCAGGGC[A/G]GAGTGGGTGGGAGCA | 71520 |
rs579259887 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61662093 | CAGTTTACAGAGCAA[A/G]TTCTAGGACAGCCAA | 71520 |
rs579687652 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656971 | GCCTTGAATTCACTA[C/T]GTAGCCCAGACCTGC | 71520 |
rs579710872 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61656643 | TGGAACAGCCACGAT[A/C]TGAGCACTGGAGAGG | 71520 |
rs579796600 | snp | C/T | | | upstream-variant-2KB | Grap | GRCm38.p3 | 11:61651623 | TGTAGACCAGGCTGG[C/T]CTCAAACTCAGAAAT | 71520 |
rs579915043 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61654347 | AGCAAGGTGTCTGTA[C/T]GTGTGTAGTGTAGTG | 71520 |
rs580217000 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61653827 | AGAGAGAGAGAGAGA[C/G]AGAGACAGAGAGAGA | 71520 |
rs580282916 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61653808 | GTGTGTGTGTGTGAG[A/T]GAGAGAGAGAGAGAG | 71520 |
rs580435604 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61671541 | TTGGCCCCCCTCCCC[A/C]TCCCCACCCCCACCC | 71520 |
rs580621385 | snp | C/T | | | upstream-variant-2KB | Grap | GRCm38.p3 | 11:61651931 | GCCAGGCAGTGGTGG[C/T]GCACACCTTTAATCC | 71520 |
rs580751333 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61659808 | GCCTAAGTATCTGGG[A/C]ACTGGGACTCTCAGA | 71520 |
rs580802329 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61657947 | CACACACACACACAT[A/G]GCTCTCTCTCTCTCT | 71520 |
rs581413796 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61655415 | GGGAAAGAGGGAGCA[A/C]TCAGCCCAGAGCCTG | 71520 |
rs581722266 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61653804 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 71520 |
rs581801325 | snp | A/C | | | upstream-variant-2KB | Grap | GRCm38.p3 | 11:61652074 | TAACTAACTAACTAA[A/C]TAAATAATAAAAAAT | 71520 |
rs581803564 | snp | A/C | | | intron-variant | Grap | GRCm38.p3 | 11:61657195 | GTAACTGGCTTTAGA[A/C]CTGTTTCAGACTGGC | 71520 |
rs582144284 | snp | C/G | | | upstream-variant-2KB | Grap | GRCm38.p3 | 11:61652755 | CCAGAGGCAGCTTGA[C/G]TTGAGAATTGGCTTG | 71520 |
rs582246028 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655433 | AGCCCAGAGCCTGGG[A/T]GAGAGGGAGCACCCA | 71520 |
rs582500298 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655450 | AGAGGGAGCACCCAG[C/T]CCAGAGCCTGGGAAA | 71520 |
rs582728159 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655443 | CTGGGAGAGAGGGAG[C/T]ACCCAGTCCAGAGCC | 71520 |
rs582865424 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655291 | GCCTGGGGGAGAGGG[A/G]GCACCCAGCCCAGAG | 71520 |
rs582924590 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61653819 | TGAGAGAGAGAGAGA[C/G]AGAGAGAGAGAGACA | 71520 |
rs583267139 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61656985 | ACGTAGCCCAGACCT[G/T]CAAACCTGCAGTGAT | 71520 |
rs583377583 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61657821 | CTCTCTCTCTCTCTC[A/T]CACACACACACACAC | 71520 |
rs583445475 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61656814 | TGTGTGTGTGTGTGT[A/G]TGTGTGTAAAATTAG | 71520 |
rs583481221 | snp | C/T | | | upstream-variant-2KB | Grap | GRCm38.p3 | 11:61651646 | TCAGAAATCCGCCTG[C/T]CTCTGCCTCCCAAGT | 71520 |
rs583718396 | snp | A/G | | | upstream-variant-2KB | Grap | GRCm38.p3 | 11:61651589 | CTCTGTATAGCTCTG[A/G]CTGTCCTGGAACTCA | 71520 |
rs583894127 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61653833 | AGAGAGAGAGAGAGA[C/G]AGAGAGAGACAGAGA | 71520 |
rs583959052 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61671543 | GGCCCCCCTCCCCCT[C/T]CCCACCCCCACCCCC | 71520 |
rs583970219 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655436 | CCAGAGCCTGGGAGA[C/G]AGGGAGCACCCAGTC | 71520 |
rs584375244 | snp | A/G | | | upstream-variant-2KB | Grap | GRCm38.p3 | 11:61651936 | GCAGTGGTGGCGCAC[A/G]CCTTTAATCCCAGCA | 71520 |
rs584439308 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61661517 | GGGTCATGATCAGGT[G/T]CTCAACAGATCCTAG | 71520 |
rs584561039 | snp | A/T | | | intron-variant | Grap | GRCm38.p3 | 11:61657980 | CTCTCTCTCTCTCTC[A/T]CTCTCTCTCTCTCTC | 71520 |
rs584663003 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61653787 | TAAGAGTGTGTGTAT[A/G]TGTGTGTGTGTGTGT | 71520 |
rs584823451 | snp | A/C | | | upstream-variant-2KB | Grap | GRCm38.p3 | 11:61652078 | TAACTAACTAAATAA[A/C]TAATAAAAAATAATT | 71520 |
rs584920440 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655416 | GGAAAGAGGGAGCAA[C/T]CAGCCCAGAGCCTGG | 71520 |
rs585216015 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61655381 | GCCTGGGTGACAGGG[A/G]GTATCCAGCCCAGAG | 71520 |
rs585542925 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61671536 | GGTCCTTGGCCCCCC[C/T]CCCCCTCCCCACCCC | 71520 |
rs585624312 | snp | A/G | | | intron-variant | Grap | GRCm38.p3 | 11:61662934 | ATTAAAAGTCTTCCT[A/G]CCTCAGAGATTCAGA | 71520 |
rs585710172 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61668446 | TGTGAATTATGTGAG[C/T]AATAAGGCTAGATAA | 71520 |
rs585969161 | snp | A/T | | | upstream-variant-2KB | Grap | GRCm38.p3 | 11:61651534 | TTAAAAGTCATTTTT[A/T]AAAAATTTTTTTGTT | 71520 |
rs586025949 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61653821 | AGAGAGAGAGAGAGA[C/G]AGAGAGAGAGACAGA | 71520 |
rs586414536 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655445 | GGGAGAGAGGGAGCA[C/T]CCAGTCCAGAGCCTG | 71520 |
rs586520283 | snp | A/C | | | upstream-variant-2KB | Grap | GRCm38.p3 | 11:61651680 | GGGATTAAAGGCGTG[A/C]GCCACCACCGCCTAG | 71520 |
rs586535726 | snp | C/G | | | intron-variant | Grap | GRCm38.p3 | 11:61653835 | AGAGAGAGAGAGACA[C/G]AGAGAGACAGAGAGA | 71520 |
rs586684911 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655295 | GGGGGAGAGGGAGCA[C/T]CCAGCCCAGAGCCTG | 71520 |
rs586706635 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | Slc5a10, Grap | GRCm38.p3 | 11:61672523 | TGGGCTTTGATGTGG[A/G]GGTGGGAGAGAGAGA | 71520 |
rs587035580 | snp | A/G | | | upstream-variant-2KB | Grap | GRCm38.p3 | 11:61652027 | TTCCAGGACAGCCAG[A/G]GCTACACAGAGAAAA | 71520 |
rs587103301 | snp | C/T | | | intron-variant | Grap | GRCm38.p3 | 11:61655383 | CTGGGTGACAGGGGG[C/T]ATCCAGCCCAGAGCT | 71520 |
rs587289996 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61657946 | TCACACACACACACA[G/T]GGCTCTCTCTCTCTC | 71520 |
rs587377550 | snp | G/T | | | intron-variant | Grap | GRCm38.p3 | 11:61657180 | CTTTCTGTGTTGACT[G/T]TAACTGGCTTTAGAC | 71520 |
rs587381117 | snp | C/T | | | upstream-variant-2KB | Grap | GRCm38.p3 | 11:61651607 | GTCCTGGAACTCACT[C/T]TGTAGACCAGGCTGG | 71520 |