SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3692649 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Rnf212 | Mm_Celera | 5:108732801 | CTGTTGTTGGAGAAG[A/C]CAAGCCTCGGAAGGA | 671564 |
rs3693219 | snp | A/G | 0.5 | 0 | intron-variant | Rnf212 | Mm_Celera | 5:108732868 | TTCTATACGACCACC[A/G]TAACTAGAACCCTTT | 671564 |
rs6161637 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B, upstream-variant-2KB | Tmed11, Rnf212 | Mm_Celera | 5:108776852 | CAATATTAAAGGCAG[A/G]TTTATTGGGAAGCTG | 671564 |
rs6162623 | snp | G/T | 0.5 | 0 | downstream-variant-500B, upstream-variant-2KB | Tmed11, Rnf212 | Mm_Celera | 5:108776987 | atagagatagataga[G/T]aGAGAGAGATAAAGA | 671564 |
rs29523509 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf212 | GRCm38.p3 | 5:108739666 | GCTACCTATGAGCTG[A/G]CAAGTATTCATGCAA | 671564 |
rs29524388 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108743879 | GGTGTATACTGATGC[A/C]TGGTTGTTTGATCTG | 671564 |
rs29525794 | snp | G/T | 0.5 | 0 | intron-variant | Rnf212 | Mm_Celera | 5:108748447 | AATATTCTCAATACA[G/T]ATATCTACTCTACAT | 671564 |
rs29545037 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Rnf212 | Mm_Celera | 5:108746083 | ACACCAGGAGCACAG[A/G]TAATATCACCGTCTT | 671564 |
rs29560272 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf212 | Mm_Celera | 5:108750521 | CCTACACTGGGGCAT[C/T]GAGCCTTCACATGAC | 671564 |
rs29564985 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Rnf212 | Mm_Celera | 5:108759429 | AGAGAGACATAGAAA[A/G]AGAGAACACAAAGGA | 671564 |
rs29565498 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Rnf212 | Mm_Celera | 5:108731531 | TACCTTGGATTAAAA[A/G]CACAATCTATAAAGT | 671564 |
rs29567306 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108731037 | GGCTACATGGTCTAA[A/G]CAATGTGCCTAGTAC | 671564 |
rs29578539 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf212 | Mm_Celera | 5:108744711 | GCTTCTACAGCAAGC[A/G]CTTGATTCACTGAGA | 671564 |
rs29583854 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf212 | Mm_Celera | 5:108744695 | GAACTTAGGTCCTCA[C/T]GCTTCTACAGCAAGC | 671564 |
rs29583921 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Rnf212 | Mm_Celera | 5:108749343 | CATTAGTGCCTACTT[G/T]TTGTGGCTTACCATC | 671564 |
rs29630134 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108739652 | CTAGAGCCATGCTTG[C/G]TACCTATGAGCTGAC | 671564 |
rs29632535 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108743806 | GAAGCCCTGCTCTGC[C/T]TTGCCCCAAAATAAA | 671564 |
rs29636631 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108738199 | GATACAGCCAACCAT[C/T]ATACTGAACATGGGG | 671564 |
rs29684608 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Rnf212 | Mm_Celera | 5:108746946 | CACTTGGTAATGACC[C/T]AGCCTTGTGAAAGAG | 671564 |
rs29726806 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf212 | Mm_Celera | 5:108745059 | CATTATCTTAAGAGT[C/T]TCTCCTAAAATGGTT | 671564 |
rs29730664 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108737531 | ACAGAAGTGGATGCT[C/T]ACAGCCATCCATTGT | 671564 |
rs29768280 | snp | C/T | 0.265928 | 0.249492 | downstream-variant-500B | Rnf212 | Mm_Celera | 5:108727614 | ATCTGCTGAATTCCT[C/T]GGCATGGCTTTCAAC | 671564 |
rs29774798 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108739647 | GCCTGCTAGAGCCAT[G/T]CTTGCTACCTATGAG | 671564 |
rs29778801 | snp | A/T | 0.455 | 0.143091 | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728665 | ACTGGAGTAGTCCAG[A/T]GGGCAGCCTGCCTGC | 671564 |
rs29780229 | snp | A/G | 0.401235 | 0.199068 | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775944 | GGCCCTTAAAAAATT[A/G]GAGGTCCAAATTATG | 671564 |
rs29813001 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Rnf212 | Mm_Celera | 5:108730774 | AGATACTCAGCAACA[C/T]ACTTGCTCTGTGTGT | 671564 |
rs29825086 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108749004 | AGACTATAACATGGA[A/G]TAATATGATTGTCCA | 671564 |
rs33069806 | snp | C/T | 0.498615 | 0.0262793 | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728834 | TCCTGTGGTGTTGAA[C/T]TCTGAGAGATGCAAG | 671564 |
rs33069833 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108749527 | CAAAGTATATAAAGG[C/T]TTGGAAATAGTTAAT | 671564 |
rs33139812 | snp | C/T | 0.455 | 0.143091 | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728569 | GAAATGAGGCTTATC[C/T]CTGCTCAGCAGCCCA | 671564 |
rs33145282 | snp | G/T | 0.5 | 0 | intron-variant | Rnf212 | Mm_Celera | 5:108746236 | TTTCCAGCTGTAAGG[G/T]ATCAGCTGTGACTGT | 671564 |
rs33167470 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Rnf212 | Mm_Celera | 5:108750161 | ACTTCTGTTCTAAAG[C/T]CATATCCTGGAACCT | 671564 |
rs33184928 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Rnf212 | Mm_Celera | 5:108749007 | CTATAACATGGAATA[A/C]TATGATTGTCCAGTG | 671564 |
rs33192125 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf212 | Mm_Celera | 5:108738722 | ATGCTAGAAAAAGCC[C/T]TTGAAAAACTCCAAC | 671564 |
rs33193420 | snp | C/G | 0.32 | 0.24 | utr-variant-5-prime | Rnf212 | Mm_Celera | 5:108775034 | GAGGCCACTGAAGTA[C/G]GAACGCACGGCTCAG | 671564 |
rs33219444 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Rnf212 | Mm_Celera | 5:108773243 | ATTTAAGAAATTTGT[G/T]TTACCTGAAAAAGTC | 671564 |
rs33221507 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108741269 | CAGAAAATTGAGACT[C/T]GATCTACCTCAAGAC | 671564 |
rs33266120 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf212 | Mm_Celera | 5:108746545 | GAGAAAGTGAGCATA[C/T]ACAAGAGGCAAGCTG | 671564 |
rs33291154 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf212 | Mm_Celera | 5:108750533 | CATCGAGCCTTCACA[C/T]GACCAAGATACCTCC | 671564 |
rs33299391 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rnf212 | Mm_Celera | 5:108744172 | AGCTGTAATAGCAGC[C/T]ACTGTCAAGGGCTGG | 671564 |
rs33302662 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108734637 | CCTCAAAGATAGAGG[G/T]CTAATGTCCAATGTA | 671564 |
rs33306843 | snp | C/G | 0.484429 | 0.0868505 | intron-variant | Rnf212 | Mm_Celera | 5:108731296 | GCCAAACCAGTCTGT[C/G]TCTGCTTCTGTGAAG | 671564 |
rs33313542 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108744012 | GAGAACTCGGCCTTG[C/T]GCCCCCTAGTGTCTA | 671564 |
rs33319338 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf212 | Mm_Celera | 5:108731921 | GGTCCATTAAGTACC[C/G]CAAGCCCATTTGAGT | 671564 |
rs33349669 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108737546 | TACAGCCATCCATTG[G/T]ACTGAGCACAGGGCC | 671564 |
rs33351395 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf212 | Mm_Celera | 5:108750480 | TCCTCCACCCACCTA[C/T]CCCCTCCCTCCTCCC | 671564 |
rs33358296 | snp | C/T | 0.48 | 0.0979796 | utr-variant-5-prime | Rnf212 | Mm_Celera | 5:108775076 | AGCTCTGCGCCTGCG[C/T]TCATTCCAGCGCATG | 671564 |
rs33358627 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108746845 | GGTCCTAGAAGTAAC[A/G]CACAATAATGAACTC | 671564 |
rs33361551 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf212 | Mm_Celera | 5:108758346 | TGAAAGAAGCTTTTG[C/T]CCCTCAAAGTCCATC | 671564 |
rs33395470 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108749207 | GGGTTACTCAATTTT[C/T]ACAAATTCTTACACC | 671564 |
rs33409090 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Rnf212 | Mm_Celera | 5:108745576 | TAAGTAGGTAAGCAA[C/T]GACAGCTTTGGTGAA | 671564 |
rs33423094 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108741163 | ACAAGTGACAGCTCA[C/T]GCTGGTAGGATGTGG | 671564 |
rs33469227 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Rnf212 | Mm_Celera | 5:108729476 | CCTAGGGGATGCTGA[C/T]CCTGTGGGAAGCATT | 671564 |
rs33525392 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108738774 | TAGAGAGATTAGGGA[C/T]AAAAGGGACATACCT | 671564 |
rs33533587 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Rnf212 | Mm_Celera | 5:108744923 | CTGGAAAGATCACTA[C/G]ACAAGACCCGTCAGG | 671564 |
rs33541655 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108741240 | CAGCCATGAAAATCA[A/C]TATGGCAGTTTCCCA | 671564 |
rs33555012 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108734770 | TGAGGAGCATCTAAA[A/G]AAATGTTCATCAGGG | 671564 |
rs33583257 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf212 | Mm_Celera | 5:108744655 | CACTCTTGTGCCTGG[G/T]TTTCATGTGGGTTTT | 671564 |
rs33600086 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf212 | Mm_Celera | 5:108740700 | AACAAGTACACTAAA[C/T]CTAATAGAAGAGAAA | 671564 |
rs33608852 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Rnf212 | Mm_Celera | 5:108773306 | GAACATGGATCATAA[A/C]ATGAGCTAAGTTAAG | 671564 |
rs33638115 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Rnf212 | Mm_Celera | 5:108747442 | AGGAGTCAGGTCAAT[A/G]TCCATTGACTCTATT | 671564 |
rs33649025 | snp | C/G | 0.32 | 0.24 | intron-variant | Rnf212 | Mm_Celera | 5:108749876 | TAATATCCCTGCTTA[C/G]TGTCTGCTGCATGTT | 671564 |
rs33675311 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Rnf212 | GRCm38.p3 | 5:108746743 | ACAAGTGCACACGTT[A/C/T]GTAGCTACCTTGGAT | 671564 |
rs33675474 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762493 | TTATGTTGATTATAT[A/G]CTATTCATGATTTTA | 671564 |
rs33707706 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Rnf212 | Mm_Celera | 5:108739921 | TGGGGAGCTCCATCT[C/G]CTGTCCTTCCCTCAA | 671564 |
rs33721445 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Rnf212 | Mm_Celera | 5:108744255 | ACCGATAACAAAGCC[C/T]GAGTCCTGCACTTAA | 671564 |
rs33725433 | snp | A/T | 0.32 | 0.24 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764373 | TTTATTTTTATTTTT[A/T]TTTTTGGTACTAAGT | 671564 |
rs33742105 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf212 | Mm_Celera | 5:108772727 | GCTGGGATTAACAGC[A/G]AAGGTAGTTTGTGCC | 671564 |
rs33745667 | snp | A/C | 0.455 | 0.143091 | intron-variant | Rnf212 | Mm_Celera | 5:108729704 | GGAGCCAGTACTGGC[A/C]GGAGTGTGAGGTTTC | 671564 |
rs33760444 | snp | G/T | 0.48 | 0.0979796 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108765786 | ATTTTCTGAGGAACC[G/T]CCAGACTGATTTCCA | 671564 |
rs45657082 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf212 | Mm_Celera | 5:108757142 | GACAACATATTTCAG[C/T]TGTAGAGGACACAGG | 671564 |
rs45658369 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108733574 | TCAACATACACCACT[C/T]ACAACTCCAGTATCA | 671564 |
rs45678667 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108743076 | AGCATTTCATGGATG[C/T]CTCGTAGAAAATATA | 671564 |
rs45689966 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108756239 | TTAGATCTGGTCTTG[C/T]CACAAGGAAATAGGA | 671564 |
rs45712136 | snp | C/G/T | 0.35503 | 0.226867 | intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108768113 | TCTCAAACACACAAA[C/G/T]GTAACAAGGGCACAT | 671564 |
rs45722035 | snp | C/T | 0.244898 | 0.249948 | nc-transcript-variant, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763868 | AGGTCCTGATGCCAA[C/T]ACTCCTGCTACCTTC | 671564 |
rs45729478 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108750078 | AGATTAAGATAGTCT[A/G]TGCTTGCAACCAGTC | 671564 |
rs45733971 | snp | A/G | 0.124444 | 0.216185 | nc-transcript-variant, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108768809 | GTGCTGCAGAGGTTT[A/G]TAAACAGTACGATAT | 671564 |
rs45748391 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B | Rnf212 | Mm_Celera | 5:108727792 | CATCTTAGCATTTAG[C/T]CATCAGGTATTTATT | 671564 |
rs45829773 | snp | C/T | 0.231111 | 0.249285 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108768209 | ATAAAATATCTCAGG[C/T]TAACTTATTCTTTGG | 671564 |
rs45837593 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108744473 | GTGTGTATGTACCTA[A/G]AGCCCAGAGACCTAA | 671564 |
rs45842875 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108776548 | AGGCCCATGTCACAT[A/G]CTCTGCCTGATAGTA | 671564 |
rs45852484 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf212 | Mm_Celera | 5:108745569 | CAGCCCTTAAGTAGG[C/T]AAGCAATGACAGCTT | 671564 |
rs45863048 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf212 | Mm_Celera | 5:108758761 | TTTCTGTAGCATTGT[A/G]TCCACACCAATCAGG | 671564 |
rs45914570 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108733696 | CAACAGTCTTGCTGG[C/T]TACAGAGTCCTTATA | 671564 |
rs45918796 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf212 | Mm_Celera | 5:108757214 | CTTTAAGTGCGGGTC[A/G]CAGCATGTTCTACTT | 671564 |
rs45928960 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108756837 | AAGGAAAACAAACCT[C/T]CCAGGTGCTGGTAAA | 671564 |
rs45949150 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Rnf212 | Mm_Celera | 5:108744933 | CACTAGACAAGACCC[A/G]TCAGGGCAATGGACT | 671564 |
rs45962641 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108732067 | AGAGTTTTAGTCTCA[C/T]GAAGTTGCCCCTGAG | 671564 |
rs45981975 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108742093 | CGTGACACTGCCTGG[A/C]TGACCAGGAATCAGA | 671564 |
rs46036161 | snp | A/C/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | GRCm38.p3 | 5:108729051 | CTATGCCACTGGAGA[A/C/T]TCACAGCACAAGGAA | 671564 |
rs46081173 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728442 | TGAATGAAAACAACT[C/T]AGAACAGGTATGTTA | 671564 |
rs46142152 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108731180 | TGGCCTTTGATGCTC[A/C]AAATGTGTGTGAGAG | 671564 |
rs46181531 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744638 | CTCAGTACCAGGCTG[C/T]GCACTGTTGTGCCTG | 671564 |
rs46217655 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762414 | TTTTCAAAAAGGCGA[A/C]TGTATTCTCCACTAC | 671564 |
rs46232570 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf212 | Mm_Celera | 5:108757209 | AGGAACTTTAAGTGC[A/G]GGTCACAGCATGTTC | 671564 |
rs46275942 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108758159 | ACCTGAGCTCTGGCT[C/T]TATATTTTTCATGTG | 671564 |
rs46368315 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108742339 | GTTGGGGAAAGAATG[A/C]AGGAGCCAGAGGGAA | 671564 |
rs46381408 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108733396 | ATTTGATTAAGACTC[C/T]TTCCTGGATATCCTG | 671564 |
rs46388378 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108748797 | AAGGAATAGCCAGAG[C/T]TTCCCAAGGCTGAGT | 671564 |
rs46390122 | snp | G/T | 0.231111 | 0.249285 | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775164 | CAGGGCCAAAAGTAC[G/T]GAGGCAAAGAAAGGC | 671564 |
rs46458169 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108743631 | GGAAGCAATTTCAGT[A/G]GGAGCCATAGGAGCA | 671564 |
rs46466042 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108747930 | AGTTGCTCCAATTTA[A/C]ATTTGGTTTTCCTGG | 671564 |
rs46482687 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf212 | Mm_Celera | 5:108759102 | GAACAAGCTGGACTC[C/T]AAGCATCTGTGTCAC | 671564 |
rs46576241 | snp | C/T | 0.32 | 0.24 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766200 | TCAGCCATGTTTCTG[C/T]CTCTTCTGAAGTTCT | 671564 |
rs46592874 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108733271 | GGGATCAAACTGAGG[C/T]TCTCATGCTTCTACA | 671564 |
rs46615601 | snp | C/T | 0.132653 | 0.220748 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766243 | AGCACAAGGAGTTTG[C/T]CTTACTTTGGTCTTT | 671564 |
rs46638633 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108755626 | TCATTCCATGGAAAT[C/G]TCTTGAAGAACACAT | 671564 |
rs46749149 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108747775 | ACTGCTGTTAACATA[C/T]ATCACTAGCCCACAC | 671564 |
rs46780428 | snp | C/T | 0.132653 | 0.220748 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764281 | AGAGGTGTGAGAGCA[C/T]TTGAACAAAACACAC | 671564 |
rs46796368 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742553 | ATATGTTTTTGTTTT[A/T]ATCCTAGGTGTGGGA | 671564 |
rs46916846 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108741543 | CAAAAGTATAAACAT[A/G]ATATGTACTCATTTG | 671564 |
rs46922111 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728711 | CAGAGTGGAAAGTTA[C/T]TTCTTTCTGCTGTTA | 671564 |
rs46923640 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Rnf212 | Mm_Celera | 5:108729285 | AAAAAAACTCCACAA[A/G]GCTATCCAGACAGCT | 671564 |
rs46929767 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108732846 | CTTACAAAGCTAAGC[A/G]TGTTCTTTCTATACG | 671564 |
rs47095397 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742199 | TCCTAATGATATTTT[G/T]CTATATTCATAGATT | 671564 |
rs47121576 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108758975 | GGCAAATGGAAAATA[A/G]CACTGTAACCCAGAT | 671564 |
rs47208341 | snp | A/T | 0.132653 | 0.220748 | synonymous-codon | Rnf212 | Mm_Celera | 5:108760083 | CTGGATATTGGAGTT[A/T]GTCTGAAGAGGAAGC | 671564 |
rs47253145 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108759611 | CTTCCCTTCATGTTG[A/G]GTATATTGCAGGTAA | 671564 |
rs47263038 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108735144 | TGTCGTTCAACAGAA[C/G]AATGGATACAGAAGA | 671564 |
rs47273444 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf212 | Mm_Celera | 5:108758363 | CCTCAAAGTCCATCT[C/T]CAAGGGCCTTGTCAT | 671564 |
rs47274875 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775796 | TCCTGGGCTATTTAC[C/T]TGTATGGAGAAAAGT | 671564 |
rs47321367 | snp | A/T | 0.260355 | 0.249785 | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762441 | CTACATAATCAAAAT[A/T]TGGTAAAAGAGTATT | 671564 |
rs47383586 | snp | A/G | 0.124444 | 0.216185 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767381 | GAACAAAGAAGATAC[A/G]CTTTCTACAAACAGC | 671564 |
rs47441266 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728543 | GGTCATATACACTTC[C/T]TGGGACAGCAGAAAT | 671564 |
rs47459598 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108742215 | CTATATTCATAGATT[A/G]GTGCCTAGCCCAATT | 671564 |
rs47540663 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108769943 | AATAAATTAATGTGA[C/T]CTATTTTATAGGTAG | 671564 |
rs47561237 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108756572 | GCTTTATAAATAGGC[G/T]CATTTGTCAGATAAC | 671564 |
rs47574550 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108757859 | CTAACTCTTCCACCA[C/T]TAAGTGCTAGTTCCA | 671564 |
rs47576439 | snp | C/T | 0.260355 | 0.249785 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766781 | GATACACACTGAGTG[C/T]TTTACAGAGGCCTTC | 671564 |
rs47673588 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf212 | Mm_Celera | 5:108732745 | GTAGTTAGTGTGTTA[C/T]GTTGTTTTGTTCTTA | 671564 |
rs47679618 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108760392 | CAGAGTCTGTGAGGC[A/G]GTAAAGAGCAAGAGA | 671564 |
rs47752770 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108732878 | CCACCATAACTAGAA[C/T]CCTTTGTATTTACTT | 671564 |
rs47760624 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108743388 | CACTTTGGAATCAGC[C/T]TGGACATGTTTTTAT | 671564 |
rs47785344 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108755762 | CAATGCCTCAGGAAT[C/T]ATTTGGAAGCCTCCA | 671564 |
rs47859254 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108760525 | AAGGATGCTGAAAAG[A/G]TCAATGGACTGAAAC | 671564 |
rs47908584 | snp | C/T | 0.124444 | 0.216185 | nc-transcript-variant, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108768714 | GAAGATACAACTGGT[C/T]TAAACATTCAACCCA | 671564 |
rs47948056 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741555 | CATAATATGTACTCA[C/T]TTGTAAATGGACATT | 671564 |
rs47950420 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108732165 | GGTGATCAGTAAATA[C/T]TGGAGAGTCACATAT | 671564 |
rs47965555 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108746949 | TTGGTAATGACCTAG[C/T]CTTGTGAAAGAGTTC | 671564 |
rs48002350 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741312 | ACCCAAATGACACTC[A/T]GTCTTACCATATGGA | 671564 |
rs48005075 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108745952 | AAATAGTAAACGATT[G/T]GGGACTCCACTACAT | 671564 |
rs48039963 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108757618 | CTGGCAGATACCAAG[A/G]CAGTCCTGTACAGAT | 671564 |
rs48078568 | snp | C/T | 0.231111 | 0.249285 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766350 | TAGAGTTAGTTGCTC[C/T]TTTCCACCTCTGCTT | 671564 |
rs48101619 | snp | A/C | 0.277778 | 0.248452 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766456 | TCCTTCTGCTTTGAT[A/C]TGAGGTCACCAGAGG | 671564 |
rs48125846 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108733359 | AATAAGCTAAGATAC[G/T]GAGAGATGGGAAAAT | 671564 |
rs48130960 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108747048 | CTTATGGTGCATTCC[C/T]AGGTTTGGGTTTCAT | 671564 |
rs48182250 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108730788 | ATACTTGCTCTGTGT[A/G]TATAACCACACAGTC | 671564 |
rs48297019 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742604 | TCCAGAGCCATTAAC[C/T]ATGATTGTCTCAAGC | 671564 |
rs48404714 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108742025 | GAACTTGTGGGAGTG[A/G]CCAACCTATGACTGG | 671564 |
rs48406286 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf212 | Mm_Celera | 5:108757401 | TGGGCTTATCCAATA[C/T]GAACTCTAAACAATA | 671564 |
rs48478612 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108747247 | CCACTTTTGCTTAAC[A/T]ATACAAGGGACCCTG | 671564 |
rs48506882 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108729799 | TTGGGATCAAAAAGC[C/T]GACTGAGCACTTGCC | 671564 |
rs48528913 | snp | A/C | 0.152778 | 0.230321 | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762334 | TTTGGCAGTTCACAA[A/C]TACCTGTAACTCCTA | 671564 |
rs48568065 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf212 | Mm_Celera | 5:108758210 | AAAAGGAACTTTAGC[C/T]TTCTGAGACAAAACA | 671564 |
rs48580693 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108758333 | CCTCCTTCAACTGTG[A/C]AAGAAGCTTTTGCCC | 671564 |
rs48617567 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf212 | Mm_Celera | 5:108759687 | GGGGACACTGACACA[C/T]GAAGTCAAGTGAGAG | 671564 |
rs48645781 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108774380 | AATGAATAAGTTGGC[A/G]TGTGATCACACAGTA | 671564 |
rs48653908 | snp | G/T | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763785 | CGGATTCTGGGAATA[G/T]GGCAGCTGTTGTCTT | 671564 |
rs48689524 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf212 | Mm_Celera | 5:108758128 | TTCAGGTCAGCAGTG[A/G]CAATATCTTCCCTAG | 671564 |
rs48722751 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rnf212 | Mm_Celera | 5:108733525 | CCCACTCCCCCATTG[C/T]CTGCACAGCCTACCC | 671564 |
rs48773851 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108773402 | TTTCTACATGCAGTA[A/C]CTGTGGTTTTGGAAG | 671564 |
rs48843091 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108742530 | AAAAATTCAGTCTTC[C/G]TATATTAATATGTTT | 671564 |
rs48890251 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108748878 | TATATGAGGCGGAAG[A/G]ACCATACCATTATAC | 671564 |
rs48962034 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108742463 | GGTCTGAGTTAGGTA[A/C]TTATGGACTCCTAAC | 671564 |
rs48984193 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Rnf212 | Mm_Celera | 5:108747570 | TTTCCCAGCCCTTTC[A/T]TGGGGTTGTTAGGGT | 671564 |
rs49009666 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108747738 | CCACTGACTAGATAC[C/T]TATGAACAGGAACAT | 671564 |
rs49046172 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775492 | AAGTACCCAGGGAAC[A/G]ATGAATGCTTGGGAG | 671564 |
rs49099570 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf212 | Mm_Celera | 5:108757996 | GGACCATAGCTGCAT[C/T]AGCGTCTGTATCTTC | 671564 |
rs49102533 | snp | A/T | 0.132653 | 0.220748 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766302 | GAGTCTAAAAGCCAG[A/T]GATTTTCCAATATCA | 671564 |
rs49155570 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763257 | AAGACTAAAATTCTG[A/G]CCATGAAGTTAAGAG | 671564 |
rs49182280 | snp | C/T | 0.142012 | 0.225474 | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762738 | GCTGCATATACAGTC[C/T]GAGTTGGAGGAGGCA | 671564 |
rs49251701 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108760162 | CTATACATAGCACAA[A/G]CAAACAGCAATTCAC | 671564 |
rs49268661 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108746778 | ATTAGAAGAATGGTC[C/T]TCATTTACAAAGCTC | 671564 |
rs49316781 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108749809 | CAGCAAAGCAAGCCC[C/T]GAGTTTCTATGACAG | 671564 |
rs49350428 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728437 | AATTGTGAATGAAAA[C/T]AACTTAGAACAGGTA | 671564 |
rs49383082 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108748873 | AATGGTATATGAGGC[A/G]GAAGAACCATACCAT | 671564 |
rs49391481 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108742988 | TCCTCCCTGGTCTCA[A/C]AGCTGCCTTGAATGA | 671564 |
rs49434241 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108746713 | TCCCTTAGAAGTGGA[C/T]ATAACTCCTGATGAA | 671564 |
rs49466297 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108744154 | TGGCATCCTAGACAC[C/T]GAAGCTGTAATAGCA | 671564 |
rs49475995 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf212 | Mm_Celera | 5:108756761 | CAGTGGAACTCTTTG[A/G]TCGGTCAGGCAAACA | 671564 |
rs49529052 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108743608 | GGACAGAAGAGAATG[G/T]TAACTGTGGAAGCAA | 671564 |
rs49565694 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108741799 | ACTGGGGGCATTTGG[A/G]GGGTGGTGTGGAAAC | 671564 |
rs49594838 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Rnf212 | Mm_Celera | 5:108733427 | GCCCACAACTTTGGA[G/T]GTGCAAGCCCTCTGC | 671564 |
rs49709897 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108744997 | ACAAGACAACTTTTG[A/G]CTAAACCACAGGAGA | 671564 |
rs49746449 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108733431 | ACAACTTTGGAGGTG[C/G]AAGCCCTCTGCTCCA | 671564 |
rs49788865 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108733896 | ACAAATTAAAGGTCA[A/G]AGTTTAATATACAAG | 671564 |
rs49795070 | snp | A/G | 0.152778 | 0.230321 | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762615 | GAGAAGCGGCACCAT[A/G]AGACTGGGGTGCTGC | 671564 |
rs49818236 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf212 | Mm_Celera | 5:108729000 | CCATGATACACAACA[C/T]CACATAGTAGCTGGC | 671564 |
rs49928214 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108747967 | ATGTTACTTCAACAG[C/T]TTCCAGATTCCTTCC | 671564 |
rs49933410 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108759960 | ATCACAGGGTCTCTG[A/G]ACTAATGTGCTCTGG | 671564 |
rs49973300 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rnf212 | Mm_Celera | 5:108774704 | ATGCGAAATATGCAG[C/T]TGGCTTTCTGGAGTT | 671564 |
rs50007177 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf212 | Mm_Celera | 5:108747993 | CTTCCTTCCTCTTGG[C/T]CTTCAGTGTCTTCAA | 671564 |
rs50023753 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108760098 | TGTCTGAAGAGGAAG[C/T]AAATGATTATGTCGA | 671564 |
rs50043624 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108744644 | ACCAGGCTGTGCACT[C/G]TTGTGCCTGGTTTTC | 671564 |
rs50044592 | snp | A/C | 0.142012 | 0.225474 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766068 | AATAGGACCTAGGTA[A/C]GACACTGAAGAAATG | 671564 |
rs50044724 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Rnf212 | Mm_Celera | 5:108747036 | GGGAAGGTGACCCTT[A/C]TGGTGCATTCCCAGG | 671564 |
rs50054737 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108759007 | TTTGTCATAGAAATG[A/G]GCTAAGGCTTCTTAG | 671564 |
rs50086064 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf212 | Mm_Celera | 5:108757262 | TAGACCTGCCATCTC[C/T]TCCCACAGGGACAGT | 671564 |
rs50120804 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775248 | TGTTGCCCACCACGA[A/G]GAAGTTTGTTGCTAA | 671564 |
rs50130618 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108743011 | TTGAATGAAGAACTG[C/T]CAGTCAAGCAGCCAG | 671564 |
rs50177984 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108739946 | CCTCAACCCTGCCTG[C/T]AGGGAGAAAACTCTA | 671564 |
rs50187514 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf212 | Mm_Celera | 5:108732186 | AGTCACATATGAAGG[C/T]CTGGAAAGTACCTCC | 671564 |
rs50204344 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763299 | TGCTTGCTGTAGTCT[A/G]CATTTCTAAACAGCA | 671564 |
rs50435845 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108755922 | AAACTGCATTATTAG[A/G]CAACTATTCCAAGAG | 671564 |
rs50483570 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741765 | ATAGAGGGAGACAGT[A/T]CTGGGAGAGACAACT | 671564 |
rs50550901 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775553 | GTCAGAGCAGGACAG[A/G]GATTCCTGGTTGTTA | 671564 |
rs50596632 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108730118 | CAGAATGAATGAGGC[C/T]TGCTCTAGGCTGAGG | 671564 |
rs50626805 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108732901 | ATTTACTTCATAGAG[C/T]TATAAAATCCATGCT | 671564 |
rs50686384 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108758093 | TACTTCTAGAGATAG[A/G]ACCATGTATAGCATG | 671564 |
rs50699967 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108739965 | GAGAAAACTCTAGGC[C/T]AACACATCTTCACAC | 671564 |
rs50704085 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108743591 | CACCAACAGTATAAG[C/T]AGGACAGAAGAGAAT | 671564 |
rs50708632 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108744306 | CACCTGCTCCTGCCT[A/T]CAGCTTTGGTGAAGA | 671564 |
rs50717628 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108757789 | AGAGAGCTGGTAGAC[A/G]GTTTGAAAAAAATGG | 671564 |
rs50766072 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108741589 | TGTTAAATAAGGTTA[A/C]TCATGCTACAGTCCA | 671564 |
rs50809435 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108747393 | TGTGCCTTGAGCAAT[G/T]TGATAGCCCAGGCAT | 671564 |
rs50853214 | snp | A/C | 0.124444 | 0.216185 | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775835 | TTTCAAGGAATTAGG[A/C]AAAAGTAGAGATTCA | 671564 |
rs50855829 | snp | C/T | 0.124444 | 0.216185 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767930 | AACTCTAAAACTATT[C/T]TTTGAAGCAATTTTT | 671564 |
rs50905070 | snp | C/T | 0.231111 | 0.249285 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767359 | TTTGCTTGTTTTCTC[C/T]TACATAGAACAAAGA | 671564 |
rs51069135 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108730237 | TCTATTATTGCAGCA[C/T]GCTTCAGCATGTATC | 671564 |
rs51100834 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108743034 | GCAGCCAGTTGGATG[A/G]CCCTTATGTCAGCAC | 671564 |
rs51110778 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108746930 | CCTACTGTTTACAGC[A/C]CACTTGGTAATGACC | 671564 |
rs51125463 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108730603 | GCATGGACTGCAGTA[A/C]GCCCAGAGTCCACAG | 671564 |
rs51127654 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf212 | Mm_Celera | 5:108756857 | GTGCTGGTAAACCCT[A/G]TTCAGCCTGGACTAA | 671564 |
rs51142445 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108744295 | CTACAGAATGCCACC[C/T]GCTCCTGCCTTCAGC | 671564 |
rs51145199 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108743087 | GATGCCTCGTAGAAA[A/C]TATATGGAAACTATA | 671564 |
rs51154085 | snp | A/G | 0.408163 | 0.193609 | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728606 | ATTTCCTGAGGACTG[A/G]GAAGATGCAATTCTA | 671564 |
rs51163460 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108756599 | TAACCTTTGGAGTTT[A/T]AAAAAAAGGCTTTTA | 671564 |
rs51197939 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108760207 | CCACACCTCTAGGGA[A/G]CATGCAGGGCAATGG | 671564 |
rs51237290 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742489 | CTAACAGTAGAATAA[G/T]ATATAGTGAGAGTTT | 671564 |
rs51269645 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108756717 | GCCCAAGTTGCCAGA[A/G]TAAGTTGCTTCATGA | 671564 |
rs51307299 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108759803 | GCACAAACAACACAG[A/G]TAAGACAGAGAATGT | 671564 |
rs51378070 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775741 | CTTTTCTCCCTTCTT[C/T]GTAAGTGTGCATGGA | 671564 |
rs51424164 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108733618 | CCAGAGGCCATGCCA[A/G]CCACCAGACTCCAAT | 671564 |
rs51430972 | snp | A/G | 0.124444 | 0.216185 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766626 | CTTAAAGAGTATCCA[A/G]GGTCACCTCTTGAAT | 671564 |
rs51431200 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742562 | TGTTTTTATCCTAGG[C/T]GTGGGATATGGGGCT | 671564 |
rs51538269 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762300 | AGTAAATGAAGGGTC[A/G]GAGAGTTGGGCACCC | 671564 |
rs51556111 | snp | C/T | 0.152778 | 0.230321 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766568 | GTAAACTAGTAATGG[C/T]CCATTTTAATGACAA | 671564 |
rs51577475 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf212 | Mm_Celera | 5:108759526 | GCTAGACCAGGCCTG[C/T]TCAGAGCCAAGAGCA | 671564 |
rs51592895 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742214 | TCTATATTCATAGAT[C/T]GGTGCCTAGCCCAAT | 671564 |
rs51608000 | snp | G/T | 0.32 | 0.24 | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766427 | TGCAGGGAGGCAAAT[G/T]TCAAACAAACACATC | 671564 |
rs51714898 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108744427 | GAACTGGCTGGTAAC[A/G]TTTTATGAACCATGT | 671564 |
rs51727123 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108729308 | AGACAGCTGCTTTAT[C/T]AGAAAGCTACTTTAT | 671564 |
rs51803411 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108742101 | TGCCTGGATGACCAG[A/G]AATCAGAGGCTAGAT | 671564 |
rs51825249 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742526 | CTTGAAAAATTCAGT[C/T]TTCGTATATTAATAT | 671564 |
rs51832518 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108756401 | AAGGCTGGATTCTGG[A/G]TAGCTGTTAGGGTAA | 671564 |
rs51842896 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf212 | Mm_Celera | 5:108733837 | AGAGAGCAAAGAATC[A/T]TTTTTTTTTAGAGTT | 671564 |
rs51921164 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108770653 | TTACATTACACTGAC[C/T]AGTGTTGTGAACTAT | 671564 |
rs51931531 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762775 | AGTACTATGCCCTGA[A/G]ATTGGACGTGGGGAA | 671564 |
rs51935726 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108760236 | GGCACATGGCAGCTA[C/T]TGAGCAACTCTGGAC | 671564 |
rs51954561 | snp | A/C | 0.48 | 0.0979796 | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108776583 | GATATGTCACATTAA[A/C]TATATAATATATGCC | 671564 |
rs51969086 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742372 | AGGACACCATGAGAA[C/T]ACTGCCCACAGAATC | 671564 |
rs52032082 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf212 | Mm_Celera | 5:108746521 | CCAGTGTAGAGTAGG[C/T]AGACACTGGAGAAAG | 671564 |
rs52044931 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Rnf212 | GRCm38.p3 | 5:108748013 | AGTGTCTTCAATACA[G/T]ATATCTACTCTACAT | 671564 |
rs52087963 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf212 | Mm_Celera | 5:108759453 | CAAAGGAATTATAAA[C/T]CTTTAACTTGCATTG | 671564 |
rs52176666 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108738512 | GGGTGGGGTAGAGAG[C/T]TTGTGGAGGGGAAAC | 671564 |
rs52401615 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108748385 | AATAGTCTCAATACA[G/T]ATATCTACTCTACAT | 671564 |
rs52526911 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108745372 | GGAGCAGAAGCACGT[A/G]GCCTGGAGAAACTGC | 671564 |
rs52562996 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf212 | Mm_Celera | 5:108770418 | ACCAAATCCTATTAC[A/G]CTTTATTACTTACAA | 671564 |
rs107883964 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108737223 | TTAGCCCAGAAGTTC[A/G]GAATACCTAAGATAC | 671564 |
rs107928152 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741868 | TCCTAGCAAAAACTC[C/T]TAGTAATGGGGGATA | 671564 |
rs108072652 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108752293 | TTTGATTTGCATTTC[C/T]CTGATGATTAAGATG | 671564 |
rs108360806 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108748467 | CTACTCTACATAATA[G/T]TCTCTTGGTGGTAGC | 671564 |
rs108742688 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108730307 | TCACTTCCAACAATT[A/C]TAGGCAGCTCTAGCA | 671564 |
rs211807050 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108729270 | AAGGATACAACAGCC[-/A]AAAAAACTCCACAAG | 671564 |
rs211820087 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108732736 | ATTTTTGCTGTAGTT[A/G]GTGTGTTACGTTGTT | 671564 |
rs211885386 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742306 | CACTAGTGGAGCCAG[A/T]GGAACTCCACAGAAG | 671564 |
rs211922315 | snp | C/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108768618 | CTGATCTTATGAAGG[C/T]ATTTTTTCAGTTTAG | 671564 |
rs211980304 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108770338 | AAATTAAAAAGAAAC[-/A]AAAAAAATACAAACA | 671564 |
rs211983349 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108774538 | CTGGTGGTGTACCTG[C/T]CCCTTTACTCGCCAA | 671564 |
rs212089611 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108769480 | AGAGACTTGATGTGC[C/T]AGGCTGGGGGGATAC | 671564 |
rs212104839 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108731008 | AATGACCCCAGGACC[C/T]AAGGTGCACATATGG | 671564 |
rs212154710 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108747906 | CAGAGGGAAGAAACA[C/T]CCTTTCTGAGTTGCT | 671564 |
rs212166817 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108729697 | AAAGACAGGAGCCAG[C/T]ACTGGCAGGAGTGTG | 671564 |
rs212270618 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108757208 | AAGGAACTTTAAGTG[C/T]GGGTCACAGCATGTT | 671564 |
rs212311172 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108756141 | CTCTTTAGAGATTCT[A/G]ATGTAAAGTTTGAGA | 671564 |
rs212426401 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741122 | GATTCCATCTTACAC[C/T]TGTCAGAATGGCTAA | 671564 |
rs212465981 | in-del | -/AAAC | | | intron-variant | Rnf212 | Mm_Celera | 5:108738687 | CTGAAAGAAACAAAA[-/AAAC]CACATGGTCATTTTA | 671564 |
rs212475376 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108748421 | TCTCAATACATATAT[C/T]TACTCTACATAATAT | 671564 |
rs212487220 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108740451 | GCGTGGTACTGGCAT[A/G]AAAAAGACAGGCTGA | 671564 |
rs212542063 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764005 | CCAGCCCAATCAAAT[A/G]TTTGTCTTTATAAGA | 671564 |
rs212547312 | in-del | -/AG | | | downstream-variant-500B, upstream-variant-2KB | Tmed11, Rnf212 | Mm_Celera | 5:108776983 | GAGATAGAGATAGAT[-/AG]AGAGAGAGAGAGATA | 671564 |
rs212557314 | in-del | -/AT | | | intron-variant | Rnf212 | Mm_Celera | 5:108745802 | TATTTGTAAGGACTC[-/AT]GTCCTGGAGCTCTAG | 671564 |
rs212598033 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108746441 | TCCAAGGAACTAATA[C/T]ATGTGGCAGGGATCT | 671564 |
rs212788638 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108739550 | GAAGTAGTTATATAA[C/G]GGAATAGACCTTGGT | 671564 |
rs212868519 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108749045 | AGTCCTAACTCTGGG[-/A]ACCCAAGCTTCACAC | 671564 |
rs212929878 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108755255 | GACTAGTGATGTCTA[A/T]TATTATCAACTTTAC | 671564 |
rs213042591 | snp | C/G | | | downstream-variant-500B | Rnf212 | Mm_Celera | 5:108728091 | TAAAAAACCAACTAA[C/G]CAACCAATCAAACAA | 671564 |
rs213052643 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108738725 | CTAGAAAAAGCCCTT[A/G]AAAAACTCCAACACC | 671564 |
rs213131667 | snp | C/T | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775131 | CAAACCGATACAGAA[C/T]CAATCCTGTGGGGAA | 671564 |
rs213163600 | snp | A/C | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108752495 | GTAAAGATCTTTTCC[A/C]AATCTGTTGGTTGCC | 671564 |
rs213274368 | snp | A/G | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762312 | GTCAGAGAGTTGGGC[A/G]CCCATGTTTGGCAGT | 671564 |
rs213284910 | snp | A/G | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108776115 | GAAGTGGTTTGAGTA[A/G]GAATAGTCTCCATAG | 671564 |
rs213303546 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108737413 | GGATCCATTCCAAAT[A/T]CAGTTTCTAAACCCA | 671564 |
rs213334152 | in-del | -/CAT | | | intron-variant | Rnf212 | Mm_Celera | 5:108760226 | CAGGGCAATGGCACA[-/CAT]TGGCAGCTATTGAGC | 671564 |
rs213358561 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108734456 | ATATGGCAGTCTCTA[C/G]ATGGTCCATCCTTTC | 671564 |
rs213370038 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108753608 | GCTAAGAGGGTCTTG[G/T]ACTGAAAGGAGAAAG | 671564 |
rs213524621 | in-del | -/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767941 | TATTCTTTGAAGCAA[-/T]TTTTTGAGTTAAAAT | 671564 |
rs213659165 | snp | A/G | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762739 | CTGCATATACAGTCT[A/G]AGTTGGAGGAGGCAA | 671564 |
rs213668522 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108742941 | TTAGGGTGAAATAAA[A/G]GTTGGAAGGGAGATA | 671564 |
rs213852142 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108772002 | CTGCATGTTCCTATG[C/T]TACCTTTCTTACTGC | 671564 |
rs214096061 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108732555 | AAACTACTCTAGTTT[C/T]TTTCTGGATGCTGTT | 671564 |
rs214167424 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108748773 | TGATATGATGAATGT[A/G]CACTTTCTAAGGAAT | 671564 |
rs214167443 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741867 | ATCCTAGCAAAAACT[C/T]TTAGTAATGGGGGAT | 671564 |
rs214278030 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108769955 | TGACCTATTTTATAG[A/G]TAGAACTAAAGGCAC | 671564 |
rs214279546 | in-del | -/CT | | | intron-variant | Rnf212 | Mm_Celera | 5:108738842 | TTAAATAGAGAGAAA[-/CT]CAATTTTTTACTAAA | 671564 |
rs214406313 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108756971 | GTCTACACAGTGAGG[C/T]CTTGTTGAGAGGGGG | 671564 |
rs214550365 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108731437 | CTTTTACAGGAAACA[C/T]CTGTGACCCTAGCCT | 671564 |
rs214676067 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108754169 | AAATTCCAAGACAGA[A/C]TAGTTCCCAGGCTGT | 671564 |
rs214680541 | snp | C/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108768540 | CCAGGGTCACTATCC[C/T]AGGAGCTGTGCCCTC | 671564 |
rs214747449 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108746254 | CAGCTGTGACTGTTA[C/T]CTTCAATATCTCTAG | 671564 |
rs214769517 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108761017 | TTGTGATAAGTACAT[-/A]AAAAATGTAATTATA | 671564 |
rs214787250 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108754977 | ATTTTTCTTTGCTTT[A/G]CCCTCATTATTTTCT | 671564 |
rs214804438 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740976 | AACAAATCAAACAAC[C/T]ATGTTTAAAAATATG | 671564 |
rs214809465 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108745817 | CGTCCTGGAGCTCTA[G/T]CTCTGAAGTCCTGTC | 671564 |
rs214947225 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108729608 | AGTTCACTGATTTAC[A/G]TATGTGTTTTTAAAA | 671564 |
rs215056824 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108756403 | GGCTGGATTCTGGGT[A/G]GCTGTTAGGGTAATG | 671564 |
rs215092064 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744848 | GGTAATGAGAGCTCC[C/T]ACACCCAGACAGGAG | 671564 |
rs215092723 | snp | C/G | | | intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108765845 | CAACAATGGAGGAGT[C/G]TTGTTGGAGGCTACT | 671564 |
rs215266256 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108740427 | TACAGAGCTATAGCA[A/G]TAAAAACTGCGTGGT | 671564 |
rs215315732 | snp | C/T | | | downstream-variant-500B | Rnf212 | Mm_Celera | 5:108727958 | CTAGGAAAGAAGAGG[C/T]AGGCATATCTCTGTG | 671564 |
rs215348147 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744456 | GTAAATTGCTTTTCT[C/T]TGTGTGTATGTACCT | 671564 |
rs215348188 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108753504 | TTTAGAATCACCTAA[A/T]CCTTTGGCATGTCAG | 671564 |
rs215381725 | snp | A/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108752390 | CTGTACCCCATTTTT[A/T]AATATAGGGTTGTTT | 671564 |
rs215578454 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108737704 | CATGGAGGGACCCAG[C/T]CTCCAGCGGCATATA | 671564 |
rs215706039 | in-del | -/GG | | | intron-variant | Rnf212 | Mm_Celera | 5:108743392 | TGGAATCAGCCTGGA[-/GG]CATGTTTTTATGCTG | 671564 |
rs215786472 | in-del | -/TC | | | intron-variant | Rnf212 | Mm_Celera | 5:108738843 | TAAATAGAGAGAAAC[-/TC]AATTTTTTACTAAAA | 671564 |
rs215794103 | in-del | -/AAACAAAACAAAACAAAACA | | | intron-variant | Rnf212 | Mm_Celera | 5:108772251 | TAGAAACCTCATCTC[-/AAACAAAACAAAACAAAACA]AAACAAAACAAAACA | 671564 |
rs215830970 | snp | A/G | | | nc-transcript-variant, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763925 | CTTCTCCAACACCAC[A/G]TCTGCCTGTATGTTG | 671564 |
rs215850945 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108749595 | TGTTCATTCCCAACT[A/G]GAAAGCAAAGTAATA | 671564 |
rs215913580 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108742688 | AGTACATGAATGCCA[A/G]GGCCTCCAGAGGTGT | 671564 |
rs215935201 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108759539 | TGCTCAGAGCCAAGA[A/G]CAGCACAGCTAAGAA | 671564 |
rs216080725 | in-del | -/A | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766100 | CAGTGGCACAGATAC[-/A]AAAGAACACAGCCTC | 671564 |
rs216114690 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108760799 | AAAAAAACAGTGGGT[A/G]TGGTGACACATGACT | 671564 |
rs216185684 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108738625 | CCCCCCAAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 671564 |
rs216217664 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108774064 | TGTATTAAAGGGCTG[C/T]AGCATTAGGAAGATT | 671564 |
rs216272623 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108761570 | AGCTGTAGTATGACA[C/T]CACAACTTGCCATTA | 671564 |
rs216355290 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767320 | AAGGAATCTCTCAAC[A/G]GTTTGGGCAGCTTCA | 671564 |
rs216459553 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108733192 | CACACACAGCAAAGC[A/G]CACTGGGAATACAGA | 671564 |
rs216507698 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108756249 | TCTTGTCACAAGGAA[A/C]TAGGAAACCTCCAGG | 671564 |
rs216730901 | in-del | -/TT | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764368 | TTTTATTTATTTTTA[-/TT]TTTATTTTTGGTACT | 671564 |
rs216812491 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | Rnf212 | Mm_Celera | 5:108728141 | ACTATACCAAATAAC[A/T]AGAAAAAGAATGCTT | 671564 |
rs216852701 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108769513 | AGGTGAAGGGTCTCT[A/G]CCCTCTCAGAGGAGA | 671564 |
rs216879554 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108733854 | TTTTTTTTAGAGTTT[A/G]ATTACTTTAATTTCT | 671564 |
rs216913950 | in-del | -/CA | | | intron-variant | Rnf212 | Mm_Celera | 5:108733415 | CTGGATATCCTGGCC[-/CA]CAACTTTGGAGGTGC | 671564 |
rs216914625 | snp | C/T | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762914 | CATTGTGCTTATTGA[C/T]AGCACACTGTACCGG | 671564 |
rs216933450 | in-del | -/AT | | | intron-variant | Rnf212 | Mm_Celera | 5:108759396 | CACACACACACAAAC[-/AT]ACACACACAGAGGGA | 671564 |
rs216980005 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108754128 | GAGGCTGAATTAAAA[G/T]GAATAGACTAATTTG | 671564 |
rs216997324 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108771673 | ATAAGAATTTCTTAC[A/G]ATTAAACTTCCTATC | 671564 |
rs217052544 | snp | C/T | | | nc-transcript-variant, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763907 | ATGTAGAATTGTCAG[C/T]TCCTTCTCCAACACC | 671564 |
rs217052558 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108753692 | GGTACTACTACCCCC[A/G]TGCTTTCCTACTGTG | 671564 |
rs217098158 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108747619 | GCTACTTCCTGTGTA[C/T]TCTACTGGCTGCTCC | 671564 |
rs217115756 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108738498 | AAGCAGGGGGGAAGG[A/G]GTGGGGTAGAGAGTT | 671564 |
rs217232284 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108740166 | CTGGTGAACCGGCTC[-/A]GAAGCTGCATCTAAT | 671564 |
rs217358971 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108773671 | AAAATCTAGGTCATC[A/G]AGACCTTTACTTCCT | 671564 |
rs217432004 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108734607 | AACCAGAAAAACAGC[C/T]ATGACAAGATTCACC | 671564 |
rs217469042 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108760698 | AGCTTTCTGAAAATG[C/T]TTGTTCATATTTCTC | 671564 |
rs217490416 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741253 | CACTATGGCAGTTTC[C/T]CAGAAAATTGAGACT | 671564 |
rs217523943 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108733097 | GAACCATAGTGTATA[A/T]TAGGAAGTCAAAGAA | 671564 |
rs217540913 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108759866 | TACAAGTAAGATAGT[-/A]AAAAAAAAAAAAACC | 671564 |
rs217566136 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108772613 | TTTTTTGTTGTTGTC[A/G]TTTTGTTTCTTGAGA | 671564 |
rs217681710 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741914 | CCATCCTCTAAAACC[C/T]GGCAAGACAGTGGGA | 671564 |
rs217683767 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108730521 | TGTGTGCTGCTCCTT[A/C]ATCCCTGTTGTCCCT | 671564 |
rs217744001 | in-del | -/TT | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108765960 | GGCAACATCTGGTCC[-/TT]TTTTTTTTTTTTCCA | 671564 |
rs217784913 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108746841 | TAAAGGTCCTAGAAG[C/T]AACGCACAATAATGA | 671564 |
rs217801556 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108731537 | GGATTAAAAACACAA[A/T]CTATAAAGTGCAACA | 671564 |
rs217909678 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108741477 | TATGAAATTTGCAGG[A/C]AAAGGGATAGAATTA | 671564 |
rs218248785 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740402 | CACCATCCATGGCTT[C/T]AAGCTGTACTACAGA | 671564 |
rs218285097 | snp | C/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767576 | ACACCATCTTCTGGC[C/T]TCTGTGGGCACCAGG | 671564 |
rs218321980 | snp | A/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766591 | AATGACAAACAAATT[A/T]ATACATGAATATATA | 671564 |
rs218331194 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108746112 | TTTGCTTGACCCAGA[A/G]AAGACCTTCTGCCTT | 671564 |
rs218464116 | in-del | -/A | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108738106 | ACTATTGATGATGCC[-/A]AAGAAGCACTTGCAG | 671564 |
rs218524547 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108744986 | TAAAGAAAGAGACAA[A/G]ACAACTTTTGGCTAA | 671564 |
rs218525316 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Rnf212 | Mm_Celera | 5:108728281 | CAGAGTCCTATTCTT[C/T]ACACGTACAGATACT | 671564 |
rs218546035 | snp | C/T | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775682 | ATTTTATTTCAAAAT[C/T]AAAATTACTTTAATA | 671564 |
rs218612657 | snp | A/G | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763395 | GATTCATGTGTTTGA[A/G]TGCTTAGCCCATAGG | 671564 |
rs218634165 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108739122 | AAAATCAGTAGATCT[C/T]CTGTACACAAATGGC | 671564 |
rs218645634 | snp | C/T | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108776726 | AATCAGAGATCCACC[C/T]GTCTCTGCCTCCCAA | 671564 |
rs218689315 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108745098 | CTCTGCTGAGGCGAA[C/G]CAAACTCTCAGCCAA | 671564 |
rs218695093 | in-del | -/CT | | | intron-variant | Rnf212 | Mm_Celera | 5:108741309 | TATACCCAAATGACA[-/CT]CTGTCTTACCATATG | 671564 |
rs218734752 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744559 | CCAAGTGGCCAAATC[A/T]GAAACTTTACAACTA | 671564 |
rs218736116 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108734910 | TGTGGAGAAAGAGGA[A/C]CACTCTTCCATTGTT | 671564 |
rs218787620 | snp | A/G | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108776329 | TGCTCCTGCCTGCAT[A/G]CCGCCATGCTCCCCA | 671564 |
rs218860727 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108737851 | GTGAGCAAAGGGAGC[A/G]GGGAAGGGATAGGGT | 671564 |
rs218866655 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108742850 | TCCCTAATCAGCAGG[A/C]AGTAGTCAAAAGAGA | 671564 |
rs218886759 | snp | C/T | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775261 | GAAGAAGTTTGTTGC[C/T]AAGGAAGCTGGGTGA | 671564 |
rs218967111 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108751851 | CAGGATGATACCCTC[C/T]AGATCCATCCATTTG | 671564 |
rs218973490 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108744008 | CTCTGAGAACTCGGC[C/G]TTGTGCCCCCTAGTG | 671564 |
rs218981287 | in-del | -/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108772701 | GGATCTCCCGTGTAT[-/G]GGTCCCAAGAGCTGG | 671564 |
rs219007231 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108743903 | TGATCTGCAAACACA[A/G]ATCCATTATATGGGA | 671564 |
rs219035281 | in-del | -/AAACAAAACAAAACA | | | intron-variant | Rnf212 | Mm_Celera | 5:108772252 | TAGAAACCTCATCTC[-/AAACAAAACAAAACA]AAACAAAACAAAACA | 671564 |
rs219104599 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108744364 | ATCAGCACCAGTAGA[A/G]TTTCTCACTTACCCA | 671564 |
rs219214783 | in-del | -/AA | | | intron-variant | Rnf212 | Mm_Celera | 5:108749313 | AAGGAAGAAATGATT[-/AA]AAAATAGTCTTCACA | 671564 |
rs219341214 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108774389 | GTTGGCGTGTGATCA[C/T]ACAGTAGAGTTCCAT | 671564 |
rs219377968 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108773030 | ATTGCCATCAAGAGC[C/T]AGAGAGATGACTCAG | 671564 |
rs219395299 | snp | G/T | | | intron-variant, utr-variant-5-prime | Rnf212 | Mm_Celera | 5:108750636 | TTGGTTGCTGGTTTA[G/T]TTCCTGGGAACTCTG | 671564 |
rs219577637 | in-del | -/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108773524 | ACACAGAACAGTGTT[-/G]GGGGCTTTGTAATTT | 671564 |
rs219690898 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742059 | AACTTAAGGCCTGTG[C/T]CATGAGAGGAAGCTC | 671564 |
rs219691157 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108749080 | GTAAGCTAAGTACCC[A/C]GGGTAGCTGGACATG | 671564 |
rs219792875 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108740627 | AAAATGTGAATAGAT[A/C]CACATCTATCACCCT | 671564 |
rs219916659 | in-del | -/CAA | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762403 | ACATAATTTTTTTTT[-/CAA]AAAGGCGAATGTATT | 671564 |
rs219933565 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108746644 | TGCTTCATTCCCTGT[G/T]AAACTCCTATTTACT | 671564 |
rs219999536 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108746629 | TCCTCAAGGCATGGA[G/T]GCTTCATTCCCTGTT | 671564 |
rs220029787 | in-del | -/CTTCT | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763094 | TTCTAGCAGGGCAAA[-/CTTCT]CTTCCGTATTGCCTC | 671564 |
rs220121999 | in-del | -/TAA | | | intron-variant | Rnf212 | Mm_Celera | 5:108758399 | TCTCCTTGCCTGCCG[-/TAA]TAATAGTCCTGATCT | 671564 |
rs220202009 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108756582 | TAGGCTCATTTGTCA[A/G]ATAACCTTTGGAGTT | 671564 |
rs220287342 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108755683 | TGGCTGCCCTGCCAT[A/G]CACAAAAGAGAATGC | 671564 |
rs220651626 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108753937 | TTATCACAAGCAGAG[A/G]TTAATGGGCTAGTCT | 671564 |
rs220731391 | in-del | -/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108743223 | TTCACCCAAGCCAGA[-/G]GGAAGCATATTCCCT | 671564 |
rs220771801 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108753732 | CACTTCATAATGTGG[A/G]TAAAAATAAACTTAT | 671564 |
rs220855648 | snp | G/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108752744 | AAGGATATAAGAATG[G/T]TTCAATTGCATTCTT | 671564 |
rs221161948 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108745876 | TGATAGCCAGCCCTA[C/T]AGGCTGAGATAGAAC | 671564 |
rs221255659 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108754284 | TTGGCCTTTAGCAGG[A/G]AAAAGAAGTAGTTTA | 671564 |
rs221399145 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108760878 | GAAGCTGGGTCTAAA[C/T]ACTGAGTTACAGAGC | 671564 |
rs221495737 | snp | C/T | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762576 | TCTCTTTCTAGCCAG[C/T]GCTCAGCCATGAGCA | 671564 |
rs221608962 | snp | A/T | | | intron-variant, utr-variant-5-prime | Rnf212 | Mm_Celera | 5:108750820 | TTCTTGGCATCCACA[A/T]TAGGGTATGGATTTT | 671564 |
rs221679803 | in-del | -/AC | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764129 | AAAGTCAATGATGTA[-/AC]ACATTTTTACATACT | 671564 |
rs221743296 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108755357 | GGTGGAAAGACCTTA[A/T]ATTTGGGTAGTACTA | 671564 |
rs221860336 | snp | C/T | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763483 | GGCTTTGAGGTCTCC[C/T]ATATTCAAGCTCTAC | 671564 |
rs221919874 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108754463 | TGTGAAAGTCAACTA[C/T]GTCCGAGGGAAGAGT | 671564 |
rs221941977 | snp | C/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764346 | TAGATGTCAATTGTC[C/T]CTTAATTTTTATTTA | 671564 |
rs221960658 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108754009 | GACAGAAATGTAGAT[A/G]GTGGAGCTCAGTTCA | 671564 |
rs222023225 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108747324 | TATTTCTAGCTACAA[C/T]CCACCCATTCACCCT | 671564 |
rs222082945 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108756675 | CATGCCCCTGTGGCC[C/T]TAGTATGGGCCAGTG | 671564 |
rs222243787 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108737984 | CAGGGACAAAAAGTC[C/G]AGTAGAGACTGAAGA | 671564 |
rs222258541 | snp | C/T | | | missense | Rnf212 | Mm_Celera | 5:108729976 | TCTGCAATGGTGGGA[C/T]TCTAACAAATTAAAC | 671564 |
rs222288252 | in-del | -/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108741768 | GAGGGAGACAGTTCT[-/G]GGAGAGACAACTGGA | 671564 |
rs222411369 | snp | C/T | | | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728416 | ATTACAGTATTTTTA[C/T]AATCAAATTGTGAAT | 671564 |
rs222594622 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108732844 | TTCTTACAAAGCTAA[A/G]CGTGTTCTTTCTATA | 671564 |
rs222636507 | snp | A/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767963 | AGTTAAAATAGAAAT[A/T]AAGAAAGTCCAGGAA | 671564 |
rs222823756 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108742961 | GAAGGGAGATAAAGG[-/A]AAAAAAAAGAGTCCT | 671564 |
rs222896004 | snp | C/T | | | downstream-variant-500B, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108769078 | CCAGGAAAAAAAAAC[C/T]CTCAACAGGCTTTTG | 671564 |
rs222949491 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108752637 | TCCTGTGCCCATGTG[C/T]TGGAGGTTTTTCCTC | 671564 |
rs222975803 | snp | C/T | | | downstream-variant-500B, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108769217 | CCACAAGAAGACAGA[C/T]AGTCAAATAACCTGG | 671564 |
rs222976480 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108754611 | ATGAAAGATGTATCA[A/G]TAAGGAAACCACTGA | 671564 |
rs223098131 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108770078 | TTGCCTGACTAGGAA[G/T]TCAGTGTTGTACTAA | 671564 |
rs223098202 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108757624 | GATACCAAGACAGTC[C/T]TGTACAGATTGCTAG | 671564 |
rs223101409 | in-del | -/TT | | | intron-variant | Rnf212 | Mm_Celera | 5:108760309 | AGGCAAAAGGGTGAG[-/TT]TTTTTTTTCCCAGAC | 671564 |
rs223160783 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108774520 | ACAAGAATTTTCCGA[C/G]GGCTGGTGGTGTACC | 671564 |
rs223198496 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108773223 | ATGTATAAAAATAAG[G/T]AAAGATTTAAGAAAT | 671564 |
rs223222998 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766471 | ATGAGGTCACCAGAG[A/G]GTGTCCTCCTAGAGG | 671564 |
rs223275126 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108760936 | CAAAAAACCCAAAAT[A/C]AATAAATAAAGCAAA | 671564 |
rs223312980 | snp | G/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767248 | GGGTTCACAAAAGAC[G/T]GCTGAAGGAGGAGCC | 671564 |
rs223314275 | snp | C/G | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764564 | TCATCTATTATGTTG[C/G]TAAGACATTTCTTCA | 671564 |
rs223362624 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108733468 | GCCACATCAGCTGCC[A/C]GAACCTCAGGTAAGC | 671564 |
rs223372718 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108740398 | GTACCACCATCCATG[A/G]CTTCAAGCTGTACTA | 671564 |
rs223434473 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108755576 | CTCAAGTTGCTATTG[C/T]CACAAAAAGGAAAAT | 671564 |
rs223458862 | snp | C/G | | | synonymous-codon | Rnf212 | Mm_Celera | 5:108729458 | CTTCTCAGTATCCAT[C/G]CCCCTAGGGGATGCT | 671564 |
rs223507878 | snp | C/T | | | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728567 | CAGAAATGAGGCTTA[C/T]CCCTGCTCAGCAGCC | 671564 |
rs223510197 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740651 | TCACCCTGCACAAAA[C/T]GCAAGTCCAAGTGGA | 671564 |
rs223537371 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | Rnf212 | Mm_Celera | 5:108728242 | TCCACCTCTAAGGGA[A/C]CCGATGCCCTCTTCT | 671564 |
rs223687311 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108739028 | ACATAAGTAATCCCC[A/G]AAATTCTACCAGGGA | 671564 |
rs223748485 | in-del | -/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108742758 | TGCTGCTCCTGGTTG[-/C]TGTTGCTGTAGTTTG | 671564 |
rs223809275 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108739860 | ATTTTACCAAGAGCA[A/G]TCTGTTTGGATGGAA | 671564 |
rs223885451 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108759478 | GCATTGAGACTGCAG[-/A]AAAGGCCAACACCGA | 671564 |
rs224023939 | snp | A/G | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763031 | ATTCAAAAGAAATAC[A/G]ATGAAAGGAAAAAGA | 671564 |
rs224190232 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108774579 | TCGGTCACTTCCCAC[G/T]GCTTTGTACGCATGC | 671564 |
rs224286820 | snp | C/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764657 | AATCCACCAGGACTA[C/T]AGAATCAGATTTGGA | 671564 |
rs224293121 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108743070 | GTTCTAAGCATTTCA[C/T]GGATGCCTCGTAGAA | 671564 |
rs224323590 | snp | C/T | | | nc-transcript-variant, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763865 | GGGAGGTCCTGATGC[C/T]AACACTCCTGCTACC | 671564 |
rs224416860 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108733560 | CACCTCTTTTCTCAT[C/T]AACATACACCACTCA | 671564 |
rs224423755 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108738170 | TCTGCCAGAGCCTGA[C/T]CAATATAGATGCAGA | 671564 |
rs224437353 | snp | C/T | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108776169 | CAAGAGGGAGTGGCA[C/T]TATTTGAAAGGATTA | 671564 |
rs224478904 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108741683 | GGGAAAAGAGAATAG[A/G]TTTTGTGGATGGTCT | 671564 |
rs224481576 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108743949 | TACAGCTTGTGGTTC[A/G]TGTCTGACATGTGTT | 671564 |
rs224512772 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108772829 | CCACAGGCCAGCAAA[C/T]TGGCTCATCTTTGGT | 671564 |
rs224614137 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108773413 | AGTAACTGTGGTTTT[A/G]GAAGAATAACTTCAG | 671564 |
rs224659436 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108737419 | ATTCCAAATTCAGTT[A/T]CTAAACCCATACACT | 671564 |
rs224660532 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744697 | ACTTAGGTCCTCATG[C/T]TTCTACAGCAAGCAC | 671564 |
rs224694956 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742665 | AGATAGTTTTGGGGA[C/T]TCTGGAGAGTACATG | 671564 |
rs224724723 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108770372 | ATCAACCAAAACCAA[A/T]CAACAATAAAACCAA | 671564 |
rs224789363 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108738419 | TAATGGGAGGGGAGG[C/T]CCTTGGTCCTGTGGA | 671564 |
rs224847815 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108732975 | GCAAATTTGAAAACA[G/T]TCAGGATGTCATTAA | 671564 |
rs224849660 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108743082 | TCATGGATGCCTCGT[A/G]GAAAATATATGGAAA | 671564 |
rs224937186 | snp | A/C | | | missense | Rnf212 | Mm_Celera | 5:108731668 | ATGGGGACTTACCTG[A/C]TAGCCTTTGTCATGC | 671564 |
rs224953219 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108739672 | TATGAGCTGTTGCAT[A/G]AGTATTCATGCAACA | 671564 |
rs225000946 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108741968 | AACATTTGACCTACA[A/G]TCTGTCCCACTTGCA | 671564 |
rs225018683 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108739097 | GATACAAGATCAACT[-/A]AAAAAAAAAAAAATC | 671564 |
rs225026343 | snp | C/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767873 | CTGATTTTGAACCCA[C/T]AGCAATCTTCCTGCC | 671564 |
rs225094443 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108745006 | TTTTGGCTAAACCAC[-/A]AGGAGACAGGAAAAC | 671564 |
rs225122173 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108742399 | AATCAATGAAGCAGG[A/G]CTCATAGAGGATCAC | 671564 |
rs225359667 | in-del | -/A | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775405 | ACCACAAAAATCAAG[-/A]AGAACCATAGGTTCC | 671564 |
rs225427651 | snp | C/T | | | missense | Rnf212 | Mm_Celera | 5:108770595 | GAGCTTGACAGATTA[C/T]GCATTCATTCTTTGT | 671564 |
rs225458536 | snp | C/T | | | nc-transcript-variant, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108768894 | AAAAATAAGGTACTC[C/T]TTATTAAAATTTTAA | 671564 |
rs225469495 | snp | A/G | | | downstream-variant-500B, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108769367 | CCAAACAACTGGAGC[A/G]AGAGGCTATCCCAAA | 671564 |
rs225503565 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740504 | CCAGACTTAAGTCCA[C/T]ACTCCTATGAGTACC | 671564 |
rs225520251 | in-del | -/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108756558 | ACAGAATGCTATGGC[-/T]TTTATAAATAGGCTC | 671564 |
rs225560665 | snp | A/C/G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108746581 | AGGTGCAGTTTATCT[A/C/G/T]TGTGCCAATGTCCAA | 671564 |
rs225648785 | in-del | -/A | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767300 | ATGTGTGGAAGAAAG[-/A]GCAGAAGGAATCTCT | 671564 |
rs225765039 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108745947 | CCATGAAATAGTAAA[C/T]GATTGGGGACTCCAC | 671564 |
rs225814247 | in-del | -/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108754677 | AAGCAATGTGTAGTA[-/C]AGTTGGATTCTATGC | 671564 |
rs225826769 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108738788 | ATAAAAGGGACATAC[C/T]TAAACACATAATTAC | 671564 |
rs225834066 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108741005 | TGGGGTATAGATCTA[A/G]ATAGAGAATTCTCAA | 671564 |
rs225953989 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108745308 | GTTTTAGGGAGAAGG[C/T]GGAGAGAAGAGGAGA | 671564 |
rs225985267 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108741566 | CTCATTTGTAAATGG[A/G]CATTAGCTGTTAAAT | 671564 |
rs226059634 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744153 | CTGGCATCCTAGACA[C/T]TGAAGCTGTAATAGC | 671564 |
rs226090469 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108745981 | ATTCTGTTAGAATTA[C/T]CAGCAGAGGAAAGGA | 671564 |
rs226223756 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108754071 | TTTGTGTTATGTTCT[A/G]GCAAAATGGCTGTAT | 671564 |
rs226266132 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108753588 | GGTGTGGTAGCATCC[A/G]GTGAGCTAAGAGGGT | 671564 |
rs226379846 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108751016 | GTATCTTGGGTATTC[C/T]AGGCTAACATTCACT | 671564 |
rs226526631 | in-del | -/AA | | | intron-variant | Rnf212 | Mm_Celera | 5:108729581 | AAGAAAAATAAGTTG[-/AA]AAAAAAAAAGAGTTC | 671564 |
rs226677263 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744615 | CTAGGGATCCCTCTC[C/T]CTGCTCCCTCAGTAC | 671564 |
rs226777407 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108749168 | TAGGAGAAGAAATGT[A/T]CATGTGTCCATAGGT | 671564 |
rs227022514 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751176 | AAAGTCCCCTATACC[A/C/G]CCCCCCCACTCCCCT | 671564 |
rs227048227 | in-del | -/TTT | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764367 | TTTTATTTATTTTTA[-/TTT]TTTTTATTTTTGGTA | 671564 |
rs227085263 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108748646 | GAAAAAGCCTGTTCA[G/T]AGAACATCCTGAGCC | 671564 |
rs227288894 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108750432 | TCAGAAACCCCCATC[A/G]CATCCCCCATCCCTC | 671564 |
rs227329496 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108757902 | GATTGTAGATAAATG[A/C]TATTTTAAGGTTCTA | 671564 |
rs227362030 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108756934 | CAGAAGCAGGTAAAT[C/T]CCGGAGTTTGAGGGC | 671564 |
rs227408261 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108749850 | GACAACCTTGTCTGA[A/G]GTCTTATGTCTAATA | 671564 |
rs227460385 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108729603 | AAAAGAGTTCACTGA[C/T]TTACGTATGTGTTTT | 671564 |
rs227903057 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108754813 | GTAGGCATGGAGTAG[A/G]GCCATCCTAAAAGAA | 671564 |
rs228001834 | in-del | -/TTGC | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108739666 | GGTACCTATGAGCTG[-/TTGC]ATGAGTATTCATGCA | 671564 |
rs228014547 | snp | C/T | | | downstream-variant-500B | Rnf212 | Mm_Celera | 5:108727644 | CACTGAGCAGCACTA[C/T]GGCCATGAGTGTGCA | 671564 |
rs228214639 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108753019 | TGATAAGTACTAACA[C/T]CTGCCTTCCAGTCCC | 671564 |
rs228216337 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108746700 | AGGTTCAGGCGACTC[C/T]CTTAGAAGTGGACAT | 671564 |
rs228246989 | snp | C/T | | | nc-transcript-variant, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763919 | CAGTTCCTTCTCCAA[C/T]ACCACATCTGCCTGT | 671564 |
rs228277341 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108754122 | TTCAGTGAGGCTGAA[A/T]TAAAAGGAATAGACT | 671564 |
rs228290310 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108754911 | TTCTAGCTCTGCATA[C/G]TGGACATGGACCAAT | 671564 |
rs228483731 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108745433 | AGAGTAGTGTAGAGG[C/T]AGATCTGCCCAATCT | 671564 |
rs228618485 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108751860 | ACCCTCCAGATCCAT[C/T]CATTTGCCTAAGAAT | 671564 |
rs228656986 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108761489 | AACTTTCAACTTCAG[A/C]TTGTATATGAACATG | 671564 |
rs228689341 | snp | G/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108752790 | CAGATGCCCATGGTG[G/T]TTTGAAGAGAGTACT | 671564 |
rs228759292 | in-del | -/AA | | | intron-variant | Rnf212 | Mm_Celera | 5:108760565 | TCTTTCCATTGACAG[-/AA]AAAAAATCTAACTTA | 671564 |
rs228905204 | in-del | -/AAATAT | | | intron-variant | Rnf212 | Mm_Celera | 5:108738550 | TGGGATAACATTTTG[-/AAATAT]AAATAAATAAAATAA | 671564 |
rs229078624 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108761338 | TGGATCTTGCTATAT[A/T]GACAAGACTGGCCTA | 671564 |
rs229106063 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108769484 | ACTTGATGTGCCAGG[C/G]TGGGGGGATACCCAG | 671564 |
rs229205658 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108770964 | AATGTTAGCAACAGT[A/C]CCTAAAAAAACTTTC | 671564 |
rs229214074 | snp | C/G | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108751361 | GTTCATACTGTTGTT[C/G]TACCTATATGGTTGC | 671564 |
rs229436920 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108757952 | GCACAGACAAAAGGG[C/T]GGTCTTCATTCACCA | 671564 |
rs229508811 | snp | G/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108768058 | AGCAGGCAGATATCT[G/T]TGAGCTCAAGGCTAG | 671564 |
rs229518206 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108741741 | AATCAGGTAGGGTGA[A/G]TGGAAGGCATAGAGG | 671564 |
rs229591218 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108771737 | ACACACACACACACA[A/C]ACACACACACACACA | 671564 |
rs229677209 | snp | A/C | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764107 | CTAGAAGAATAGGAC[A/C]TTTAGCAAAGTCAAT | 671564 |
rs229854639 | snp | C/T | | | downstream-variant-500B | Rnf212 | Mm_Celera | 5:108728095 | AAACCAACTAAGCAA[C/T]CAATCAAACAAACCA | 671564 |
rs229884790 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108749486 | AGTAGATTAATTAAT[G/T]AAATTGATTTCTCCT | 671564 |
rs229946739 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108759349 | TAAGCTTGGGTTGTA[G/T]AGCAATTTCTATGTT | 671564 |
rs229954301 | in-del | -/ATTTTCCG | | | intron-variant | Rnf212 | Mm_Celera | 5:108774511 | CCGCAGTCTACAAGA[-/ATTTTCCG]AGGGCTGGTGGTGTA | 671564 |
rs230067811 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108731798 | TACCAGATCATACCT[C/T]CTGGTGCTTCTCTAA | 671564 |
rs230131887 | in-del | -/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108738463 | ATGAGGTGGGAGTGT[-/G]GGGGGGAAGACCCTC | 671564 |
rs230165153 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108738760 | TATGATAAAAGTCTT[A/G]GAGAGATTAGGGATA | 671564 |
rs230329349 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766932 | GTGAGAACAATAGAG[A/G]TGAGAGTTACAGAGA | 671564 |
rs230380697 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108774491 | GGCTGGACAACAAAA[C/T]GAAACCGCAGTCTAC | 671564 |
rs230459543 | in-del | -/CTAATTTGGC | | | intron-variant | Rnf212 | Mm_Celera | 5:108740211 | TACTTTTAATCTGGT[-/CTAATTTGGC]CTATACTACATAGGT | 671564 |
rs230462102 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108742958 | TTGGAAGGGAGATAA[A/G]GGAAAAAAAAAGAGT | 671564 |
rs230492436 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108756035 | AGAGCTGAGTCATGT[C/T]AGATCTCTAGAGAAA | 671564 |
rs230529217 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108734523 | TAACTGACTTGTGCA[C/T]ATTCCATACATATAC | 671564 |
rs230582874 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108743864 | ATGGTCCTTCCACCT[A/G]GTGTATACTGATGCC | 671564 |
rs230622007 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108756727 | CCAGAGTAAGTTGCT[C/T]CATGAAGGTTGCCCA | 671564 |
rs230709375 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108737094 | ctcagctattaaaaa[A/C]aatgaattcatgaag | 671564 |
rs230754422 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108772016 | GTTACCTTTCTTACT[C/G]CATGTTGCTTTATTG | 671564 |
rs230832036 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108769967 | TAGGTAGAACTAAAG[A/G]CACTGGTTTAAGCCC | 671564 |
rs230848923 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740307 | CTTAAAAGGATAATA[C/T]TCAACTTCACATAGA | 671564 |
rs231080371 | snp | A/G | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763698 | GGTGGTGGCAGAAAG[A/G]GAAGGGGAAAAGAGA | 671564 |
rs231106027 | snp | A/C | | | downstream-variant-500B | Rnf212 | Mm_Celera | 5:108727962 | GAAAGAAGAGGCAGG[A/C]ATATCTCTGTGAGTT | 671564 |
rs231113068 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108747795 | CTAGCCCACACATTA[C/G]AGAATTCATTAGTCA | 671564 |
rs231183328 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108739467 | TATTAGGTGAGCCAA[A/G]GGGGGATTTTTATTG | 671564 |
rs231254975 | snp | A/G | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762723 | CTAAGATTGGCCCTC[A/G]CTGCATATACAGTCT | 671564 |
rs231495252 | in-del | -/AAG | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763242 | GTGTAAAAAAAAAAA[-/AAG]AGACTAAAATTCTGA | 671564 |
rs231565816 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108771847 | GTCACTTCCAAGAGT[C/T]AGCTCTTATAGTAGG | 671564 |
rs231566388 | in-del | -/CA | | | intron-variant | Rnf212 | Mm_Celera | 5:108771697 | TCCTATCTCATACAC[-/CA]CACACACACACACAC | 671564 |
rs231584485 | in-del | -/CT | | | intron-variant | Rnf212 | Mm_Celera | 5:108732806 | TTGGAGAAGACAAGC[-/CT]CTCGGAAGGACAGCC | 671564 |
rs231597040 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108761130 | TGGAAGACAGTGATG[A/C]TGAGGGTGATTTGAA | 671564 |
rs231667936 | in-del | -/AA | | | intron-variant | Rnf212 | Mm_Celera | 5:108742960 | GAAGGGAGATAAAGG[-/AA]AAAAAAAAAGAGTCC | 671564 |
rs231741071 | in-del | -/TTTTT | | | intron-variant | Rnf212 | Mm_Celera | 5:108733837 | GAGAGCAAAGAATCA[-/TTTTT]TTTTTTTTTAGAGTT | 671564 |
rs231817481 | in-del | -/ATAGATAGATAT | | | downstream-variant-500B, upstream-variant-2KB | Tmed11, Rnf212 | Mm_Celera | 5:108776989 | GAGATAGATAGAGAG[-/ATAGATAGATAT]AGAGAGATAAAGAAT | 671564 |
rs231823573 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108737338 | CCATTGGAGGAAATA[C/T]AGAGACAAATTTTGA | 671564 |
rs231882631 | snp | A/G | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108776647 | CCACCCCCTTTTTGG[A/G]GAAAGGTCTTTTGTG | 671564 |
rs231970723 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108773303 | GTATGAACATGGATC[A/T]AACATGAGCTAAGTT | 671564 |
rs231971164 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108732212 | CCTCCAGAAGAATGC[C/T]CCCTTTGCACTTTAG | 671564 |
rs232026756 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742197 | ATTCCTAATGATATT[G/T]TTCTATATTCATAGA | 671564 |
rs232089227 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108745835 | CTGAAGTCCTGTCAC[C/T]TCTAATAAAACCCCC | 671564 |
rs232168951 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108742831 | GGCCCCAAGAAACAC[-/A]ATGTCCCTAATCAGC | 671564 |
rs232183101 | snp | A/G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108743969 | TGACATGTGTTCTAC[A/G/T]TTTGCTATGTGACTG | 671564 |
rs232195583 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108752412 | GGGTTGTTTGATTCT[C/T]TGGAGTCTAACTTCT | 671564 |
rs232197103 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108740438 | AGCAATAAAAACTGC[A/G]TGGTACTGGCATGAA | 671564 |
rs232227114 | snp | C/T | | | intron-variant, utr-variant-5-prime | Rnf212 | Mm_Celera | 5:108750725 | CTTTCTCTAACTCCT[C/T]AAGCATCTGCCTTTG | 671564 |
rs232249490 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108744896 | GAGGACCCATATGAG[A/G]AGAACTAGGGTCTGG | 671564 |
rs232276328 | snp | G/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108748044 | AATATTCTCAATACA[G/T]ATATCTACTCTACAT | 671564 |
rs232282350 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108746344 | CTTCTTCACCATTAA[C/T]ATGGGAATCTGGAGG | 671564 |
rs232523219 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108740935 | TAATATCCAAAAGAA[A/G]TAAAGAACTCAAGAA | 671564 |
rs232545690 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742593 | GCTTCAGTTTGTCCA[G/T]AGCCATTAACCATGA | 671564 |
rs232818098 | snp | A/C | | | downstream-variant-500B, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108769298 | TTGGACCTAGGCTTC[A/C]TCCCCTAACACACAA | 671564 |
rs232828325 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108739336 | ATTTGTTTTGGAGGG[C/G]GTCTGCCTCTGGATA | 671564 |
rs232950156 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741534 | ACCCAGGCCCAAAAG[G/T]ATAAACATAATATGT | 671564 |
rs232965130 | in-del | -/CCTT | | | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728808 | TGAGCACCACAACCC[-/CCTT]CCTTCTTAGTTCCTG | 671564 |
rs233070466 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108745118 | CTCTCAGCCAACCAG[C/T]TGTTGTGGATTGCCC | 671564 |
rs233130504 | in-del | -/AAA | | | intron-variant | Rnf212 | Mm_Celera | 5:108759865 | TACAAGTAAGATAGT[-/AAA]AAAAAAAAAAAAAAC | 671564 |
rs233194578 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108746121 | CCCAGAGAAGACCTT[C/T]TGCCTTGCAAAGTTT | 671564 |
rs233267771 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108746619 | AAGCATCTCCTCCTC[A/G]AGGCATGGATGCTTC | 671564 |
rs233275893 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108756368 | CTAACCAAGACTTGA[C/G]TGGAGGTAAGAATCC | 671564 |
rs233290864 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108748631 | AAACTAAACTCATAG[-/A]AAAAAGCCTGTTCAT | 671564 |
rs233300533 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108760958 | AAAGCAAAACAAAAC[-/A]AAACAAATCAAATCA | 671564 |
rs233303336 | in-del | -/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744449 | AACCATGTAAATTGC[-/T]TTTTCTCTGTGTGTA | 671564 |
rs233311766 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108755380 | TAGTACTATTCCATG[C/T]GCTGAGGTTTTAGAT | 671564 |
rs233363381 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740414 | CTTCAAGCTGTACTA[C/T]AGAGCTATAGCAATA | 671564 |
rs233558448 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108749538 | AAGGTTTGGAAATAG[C/T]TAATTGCATGATTTT | 671564 |
rs233686866 | snp | A/C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108742695 | GAATGCCAAGGCCTC[A/C/T]AGAGGTGTGATAGGC | 671564 |
rs233707970 | snp | A/T | | | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728618 | CTGGGAAGATGCAAT[A/T]CTAGCAACAGCATCC | 671564 |
rs233730234 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108749017 | GAGTACTATGATTGT[C/T]CAGTGAAGATCTAAG | 671564 |
rs233762970 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | Rnf212 | Mm_Celera | 5:108728193 | GAGCTCAGATGCCAG[A/C]ATCCATGTTAGGCTG | 671564 |
rs233911474 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108749596 | GTTCATTCCCAACTG[A/G]AAAGCAAAGTAATAC | 671564 |
rs234090697 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744756 | CGTAAGTCATTTTTC[G/T]ATTGTTCCACCTATA | 671564 |
rs234244883 | in-del | -/ATTATTTACC | | | intron-variant | Rnf212 | Mm_Celera | 5:108770030 | TGAACAACCCTCTTA[-/ATTATTTACC]ATGACTTTTATGAAA | 671564 |
rs234387310 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108760761 | AGAACTCACAATAGC[C/T]ACTTTCAAAATTAGG | 671564 |
rs234457107 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108759743 | ATAGCAAGTGTGTCA[A/C]TAGGGAGAAGAGTAG | 671564 |
rs234471423 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108755272 | ATTATCAACTTTACA[C/G]AATCTATAATTTAAT | 671564 |
rs234537355 | snp | C/T | | | intron-variant, utr-variant-5-prime | Rnf212 | Mm_Celera | 5:108750638 | GGTTGCTGGTTTATT[C/T]CCTGGGAACTCTGGT | 671564 |
rs234658997 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108743538 | GACAGCAGTGGAACA[A/G]TAAAGAACAATAACC | 671564 |
rs234728253 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108744945 | CCCGTCAGGGCAATG[A/G]ACTAGCAATCTAAGT | 671564 |
rs234746762 | in-del | -/TACCAAATTTATAGGTC | | | intron-variant | Rnf212 | Mm_Celera | 5:108744192 | TCAAGGGCTGGGGAA[-/TACCAAATTTATAGGTC]TACATAATCACTATA | 671564 |
rs234763191 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108772658 | GTCTTACAACTCAAT[A/C]TGTAAACCAGTCTGG | 671564 |
rs234788312 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108753659 | ACCTGTTTTCTGACT[A/G]CAGAAGCAATATGAC | 671564 |
rs234903329 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108733130 | CTGTCTGAAAAGACT[A/G]CATTCTCGATAACTC | 671564 |
rs235065821 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108753717 | ACTGTGAAGGACTGC[C/T]ACTTCATAATGTGGA | 671564 |
rs235101967 | snp | A/G | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762962 | GGCCACAAGAAGGGG[A/G]CCAAGCTGACTCTTG | 671564 |
rs235176714 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108754129 | AGGCTGAATTAAAAG[A/G]AATAGACTAATTTGT | 671564 |
rs235654891 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108756174 | TGTCCTCCTAAAGGA[C/T]ATAAAATATCTACAC | 671564 |
rs235666460 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108743512 | GAGCTGGTTAACATT[-/A]AGAAGGACAAGACAG | 671564 |
rs235732707 | snp | C/T | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762596 | AGCCATGAGCATCTC[C/T]TGGGAGAAGCGGCAC | 671564 |
rs235732784 | snp | A/T | | | downstream-variant-500B, upstream-variant-2KB | Tmed11, Rnf212 | Mm_Celera | 5:108776754 | CAAGTGATGGGATTA[A/T]AGGCATTGCCAGCAG | 671564 |
rs235764556 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751176 | AAGTCCCCTATACCA[-/C]CCCCCCCACTCCCCT | 671564 |
rs235843974 | snp | C/T | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763417 | GCCCATAGGGAAGGG[C/T]ACTATTAGGAGGTGT | 671564 |
rs235848943 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108754348 | AAGTAGCTGTAATTT[C/T]TAAAGAGATTAACAT | 671564 |
rs235918687 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108731476 | AAAGAGCTACTGTGC[A/T]TCTATCTATTCACTA | 671564 |
rs235919816 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108737856 | CAAAGGGAGCGGGGA[A/T]GGGATAGGGTAGTTT | 671564 |
rs235986707 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108734929 | TCTTCCATTGTTGGT[A/G]GGATTAGAAGTTGGT | 671564 |
rs236036821 | snp | C/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767399 | TTCTACAAACAGCCA[C/T]AGAATAGTCATAATT | 671564 |
rs236211577 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108756445 | TGGATAGAGTGCTGG[A/T]TAACAGAGTGAGGTC | 671564 |
rs236271854 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108760944 | CCAAAATCAATAAAT[-/A]AAGCAAAACAAAACA | 671564 |
rs236358667 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108757998 | ACCATAGCTGCATTA[G/T]CGTCTGTATCTTCCC | 671564 |
rs236402155 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108744581 | TTACAACTAAGCTGG[A/G]CTGGCCGGCTAGTGC | 671564 |
rs236495724 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108754200 | GCCATGGTTACTGCT[C/T]ACTGCTCTTATCTTT | 671564 |
rs236582755 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767714 | CCCAACACCAAAGAC[A/G]CTGGTCACAGTGCTA | 671564 |
rs236645472 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740477 | GCTGATAAATGAAAT[C/T]GAGTAGAAGATCCAG | 671564 |
rs236747540 | snp | A/C | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108752557 | CTTTGCAAATGTATG[A/C]GATCCCATTTGTCAA | 671564 |
rs236782624 | snp | C/T | | | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728939 | GAGCAACAGGTCTCA[C/T]CTGCAACTTGACTTC | 671564 |
rs236789937 | snp | G/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763962 | TTCCTGTCTTAATGA[G/T]AATAGACCAAACCTC | 671564 |
rs236866165 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108738713 | TTTTATTAGATGCTA[A/G]AAAAAGCCCTTGAAA | 671564 |
rs236914932 | in-del | -/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108738625 | CCCCCCAAAAAAAAA[-/G]AAAAAAAAAAAAAAA | 671564 |
rs236927767 | snp | A/G | | | downstream-variant-500B | Rnf212 | Mm_Celera | 5:108727646 | CTGAGCAGCACTACG[A/G]CCATGAGTGTGCAGC | 671564 |
rs236947657 | snp | G/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767971 | TAGAAATAAAGAAAG[G/T]CCAGGAAAGGTGGGA | 671564 |
rs236993745 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108739172 | TGGGGGAAACAATAT[C/T]CTTCACAACTGAAAG | 671564 |
rs237063742 | snp | C/T | | | downstream-variant-500B, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108769090 | AACCCTCAACAGGCT[C/T]TTGGAAAGGATAACA | 671564 |
rs237105288 | snp | A/G | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762293 | ATTTAAAAGTAAATG[A/G]AGGGTCAGAGAGTTG | 671564 |
rs237158327 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741362 | CAACAGCTTTATTCA[C/T]AAGAACCTGGAAACA | 671564 |
rs237163374 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108749812 | CAAAGCAAGCCCTGA[A/G]TTTCTATGACAGAAG | 671564 |
rs237224083 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740634 | GAATAGATCCACATC[C/T]ATCACCCTGCACAAA | 671564 |
rs237240475 | in-del | -/A | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766388 | GTTACACTTCACTTG[-/A]AAATTCATTATTCCT | 671564 |
rs237336078 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108772852 | TCTTTGGTAAAGACA[C/T]TTGCTACTAAGTATG | 671564 |
rs237367615 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108746005 | GAAAGGACAAGTAAT[A/C]TCCTGAATGATCTTG | 671564 |
rs237423297 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108759632 | TTGCAGGTAATCCAG[G/T]GAATCAAGTCAAATG | 671564 |
rs237440541 | snp | C/T | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775111 | CAAGGCCGCGCCTTC[C/T]CGCCCAAACCGATAC | 671564 |
rs237448846 | in-del | -/AG | | | intron-variant | Rnf212 | Mm_Celera | 5:108738624 | CCCCCCCAAAAAAAA[-/AG]AAAAAAAAAAAAAAA | 671564 |
rs237468425 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108732714 | TTAGTCTATGCCACT[C/G]CAGGTAATTTTTGCT | 671564 |
rs237560443 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108746630 | CCTCAAGGCATGGAT[A/G]CTTCATTCCCTGTTA | 671564 |
rs237690646 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108773045 | CAGAGAGATGACTCA[A/G]CAGTTAAGAACTAGT | 671564 |
rs237696903 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108756984 | GGCCTTGTTGAGAGG[A/G]GGAGGGCGGGGAACT | 671564 |
rs237702182 | in-del | -/TT | | | intron-variant | Rnf212 | Mm_Celera | 5:108732809 | GAGAAGACAAGCCTC[-/TT]GGAAGGACAGCCTGA | 671564 |
rs237744205 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108759548 | CCAAGAGCAGCACAG[C/T]TAAGAAAGAAAGAAC | 671564 |
rs237793495 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108755129 | AGTGTTGGAACCATT[-/A]AAAATTATGCAGACT | 671564 |
rs237811807 | snp | C/G/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108732821 | CCTCGGAAGGACAGC[C/G/T]TGACAGCTTCTTACA | 671564 |
rs237914878 | snp | A/T | | | nc-transcript-variant, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108768905 | ACTCCTTATTAAAAT[A/T]TTAAACAGCTAAATA | 671564 |
rs238006349 | in-del | -/AAG | | | intron-variant | Rnf212 | Mm_Celera | 5:108738623 | CCCCCCCCAAAAAAA[-/AAG]AAAAAAAAAAAAAAA | 671564 |
rs238064381 | snp | C/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108768582 | CTAATTAAGAAAATG[C/T]ACAACAGGTCGTCCT | 671564 |
rs238066308 | in-del | -/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108741186 | GGATGTGGAGCAAGA[-/G]GAACACTCCTCCATT | 671564 |
rs238072759 | in-del | -/TTA | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764371 | TATTTATTTTTATTT[-/TTA]TTTTTGGTACTAAGT | 671564 |
rs238241631 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742078 | GAGAGGAAGCTCACA[C/T]GTGACACTGCCTGGA | 671564 |
rs238337215 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108729610 | TTCACTGATTTACGT[A/G]TGTGTTTTTAAAAAT | 671564 |
rs238428416 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108755085 | ATGAACTATGACTCA[G/T]AAGAGACTCTACACT | 671564 |
rs238623280 | snp | A/G | | | synonymous-codon | Rnf212 | Mm_Celera | 5:108749413 | TGAAACTGAATTTTT[A/G]ATTTTGTTGAAAGCT | 671564 |
rs238748874 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108739774 | CTCTGAAGAAAGAAA[C/T]TGAAGATATCAGAAG | 671564 |
rs238766105 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742603 | GTCCAGAGCCATTAA[C/T]CATGATTGTCTCAAG | 671564 |
rs238767499 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108749895 | CTGCTGCATGTTAAG[A/T]TGTCTGTTCATAGTA | 671564 |
rs238822679 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108733837 | AGAGAGCAAAGAATC[-/A]TTTTTTTTTAGAGTT | 671564 |
rs239024244 | snp | C/G | | | missense | Rnf212 | Mm_Celera | 5:108745691 | GAGGTGGACTAATCA[C/G]AGAGATTCTTGAAGG | 671564 |
rs239131777 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108737757 | ACATCAATGAGAGGA[A/G]AGGCCCTTGGTCTTG | 671564 |
rs239221824 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108745082 | AAATGGTTCATAGTA[C/T]CTCTGCTGAGGCGAA | 671564 |
rs239259623 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108774323 | AGTAGCAGCATTTGC[C/T]ACTTACAAATCTGGA | 671564 |
rs239283010 | snp | C/T | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108776331 | CTCCTGCCTGCATGC[C/T]GCCATGCTCCCCAAC | 671564 |
rs239341474 | snp | A/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108752745 | AGGATATAAGAATGT[A/T]TCAATTGCATTCTTC | 671564 |
rs239363726 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744365 | TCAGCACCAGTAGAG[C/T]TTCTCACTTACCCAC | 671564 |
rs239429405 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108751221 | ACTTCATGGCTCTAG[C/T]GACCCCTGTATTGGG | 671564 |
rs239464165 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108760824 | ATGACTTTAATCCCA[A/G]CACTCAGTAGGCAGA | 671564 |
rs239487263 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744678 | TGGGTACCTGGGGAA[C/T]GGAACTTAGGTCCTC | 671564 |
rs239502311 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108737649 | GAACCAACCAGTACC[C/T]CCAGATTCCCAGGGA | 671564 |
rs239524520 | in-del | -/CAGACAAAAGGGCGGTCTT | | | intron-variant | Rnf212 | Mm_Celera | 5:108757940 | CTCTAGGTAACAGCA[-/CAGACAAAAGGGCGGTCTT]CATTCACCAAACAAC | 671564 |
rs239551239 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108749866 | GTCTTATGTCTAATA[G/T]CCCTGCTTACTGTCT | 671564 |
rs239592782 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108773879 | TCTCTAGAGAGCTCA[A/C]ACAAAACAGGGTCTA | 671564 |
rs239690246 | in-del | -/ATGAC | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108742174 | TGAATGAATGAATGA[-/ATGAC]ATAATTCCTAATGAT | 671564 |
rs239810765 | in-del | -/CTC | | | intron-variant | Rnf212 | Mm_Celera | 5:108774606 | ATGCGGCCCCCGGCT[-/CTC]TCCCCCCACCCCCCA | 671564 |
rs239854463 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108754025 | GTGGAGCTCAGTTCA[C/T]GAGGGCTCAGAGGAG | 671564 |
rs239944523 | snp | A/G | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763502 | TTCAAGCTCTACCCA[A/G]TGTTAATCCAGTCTC | 671564 |
rs240020353 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108754464 | GTGAAAGTCAACTAC[A/G]TCCGAGGGAAGAGTT | 671564 |
rs240080059 | in-del | -/AA | | | intron-variant | Rnf212 | Mm_Celera | 5:108760780 | TTCAAAATTAGGGAG[-/AA]AAAAAAAAACAGTGG | 671564 |
rs240209041 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108769572 | AGATGACTGGGAAGA[A/G]GGGCAGTGAGCAGTG | 671564 |
rs240248858 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741936 | ACAGTGGGATTGAGA[C/T]ACCAACCTGGCCACA | 671564 |
rs240308454 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741815 | GGGTGGTGTGGAAAC[C/T]TAGTAGAATGGAAAC | 671564 |
rs240445191 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108747978 | ACAGCTTCCAGATTC[C/T]TTCCTTCCTCTTGGT | 671564 |
rs240481938 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108731237 | GGAAAAAGGTGTGGC[C/T]GAGAGAAAGATATGT | 671564 |
rs240555282 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108756705 | GTAGCTGAGGGAGCC[C/T]AAGTTGCCAGAGTAA | 671564 |
rs240615707 | snp | A/C | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767335 | AGTTTGGGCAGCTTC[A/C]CTGGTTCATTTGCTT | 671564 |
rs240637516 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108755955 | AGTTCAGACAACATA[C/T]TTGATTTGTTTACAT | 671564 |
rs240638763 | in-del | -/GA | | | intron-variant | Rnf212 | Mm_Celera | 5:108750521 | CTACACTGGGGCATC[-/GA]GAGCCTTCACATGAC | 671564 |
rs240698103 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108747357 | GGTCAACACAGTAAA[C/G]AGCTTTGCTAGACAC | 671564 |
rs240794589 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108745115 | AAACTCTCAGCCAAC[C/T]AGTTGTTGTGGATTG | 671564 |
rs240833309 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108753977 | CAATGGTGGGGAATT[A/G]GAAGAAAAAGAACAC | 671564 |
rs241043003 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108770198 | ATGAGGGTTTAAAAG[C/G]AAATCCTGATGGTAT | 671564 |
rs241094369 | snp | G/T | | | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728425 | TTTTTACAATCAAAT[G/T]GTGAATGAAAACAAC | 671564 |
rs241115641 | snp | C/G | | | downstream-variant-500B, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108769255 | GGGCTCTCCGAGACT[C/G]AACTACCAACCAAAG | 671564 |
rs241173741 | in-del | -/TTTC | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108744667 | GGTTTTCATGTGGGT[-/TTTC]ACCTGGGGAACGGAA | 671564 |
rs241182884 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108758573 | ACACTGTATTATCCA[A/T]GTTATAGCTCCATCT | 671564 |
rs241253066 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108731640 | GGTTTTGTTTGGCTT[A/G]TGTTTTGCCCCAATG | 671564 |
rs241271426 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108739314 | GAGGGAACCAGGGAG[A/G]AGGGGTATTTGTTTT | 671564 |
rs241495671 | in-del | -/CCAGAGT | | | intron-variant | Rnf212 | Mm_Celera | 5:108730606 | TGGACTGCAGTAAGC[-/CCAGAGT]CCACAGGGTTATTCA | 671564 |
rs241496637 | snp | C/T | | | intron-variant, utr-variant-5-prime | Rnf212 | Mm_Celera | 5:108750935 | AGTATTTTGTTCCCC[C/T]TTTGAAGAAGGATGA | 671564 |
rs241500513 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108730571 | CAACTTTTCTCTTGC[C/T]TATGCATTCTAGATG | 671564 |
rs241515839 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108738815 | TTACAGCAAGCCACT[A/G]GCCAACATCAAATTA | 671564 |
rs241540974 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108752721 | CAACTTTGAGTTGAG[C/T]TTTGTACAAGGATAT | 671564 |
rs241604836 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108760892 | ACACTGAGTTACAGA[A/G]CAGTCAGAACTGCAT | 671564 |
rs241640566 | snp | A/G | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775332 | ATCAGGCCTCACGGT[A/G]GAGACAGGCCCAGGG | 671564 |
rs241648242 | in-del | -/ACAA | | | downstream-variant-500B, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108769043 | TGAACAAACAAACAT[-/ACAA]ACAAACAAACAAAAA | 671564 |
rs241662227 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108760962 | GCAAAACAAAACAAA[A/C]AAATCAAATCAAATA | 671564 |
rs241806769 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108751108 | TTTTCTTTCTTTTTT[C/T]CCCCAACTTTTTATT | 671564 |
rs242131330 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108733519 | ACTACTCCCACTCCC[C/T]CATTGTCTGCACAGC | 671564 |
rs242189318 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108732872 | ATACGACCACCATAA[C/T]TAGAACCCTTTGTAT | 671564 |
rs242232183 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108761401 | TTAAAGGTATTGGCT[A/T]CTACTCTGTACTCTA | 671564 |
rs242257694 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108743908 | TGCAAACACAAATCC[A/C]TTATATGGGAAACAT | 671564 |
rs242348049 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108773494 | CTGTGTACCACCCAA[A/G]GCCTCAAACTAGTCA | 671564 |
rs242391693 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108749122 | CAGGCACTTAGTAGG[A/T]GTGATTTGGTGATTT | 671564 |
rs242456859 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108774801 | CTCTGTCCCACCCAC[A/G]GGAGTGAAGCCACGC | 671564 |
rs242458778 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108760623 | TTTTAATTTAATTAT[A/G]TGTATAATGTGTGTG | 671564 |
rs242562436 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108733040 | ATGAAATATTATTAA[A/C]CACTACAAAAATTAG | 671564 |
rs242599831 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108756749 | GGTTGCCCAAAGCAG[A/T]GGAACTCTTTGATCG | 671564 |
rs242624303 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742675 | GGGGACTCTGGAGAG[G/T]ACATGAATGCCAAGG | 671564 |
rs242690734 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108733598 | AGTATCAGCTCCCTG[C/T]CCCACCAGAGGCCAT | 671564 |
rs242709242 | in-del | -/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108758757 | CAGATTTCTGTAGCA[-/T]TGTATCCACACCAAT | 671564 |
rs242721253 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108729326 | AAAGCTACTTTATTT[A/C]GTTACATCATCTCTC | 671564 |
rs242870805 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742285 | ATGCAAAGACCTGTA[G/T]ACAAACACTAGTGGA | 671564 |
rs242879040 | snp | C/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764727 | GATTCTAAGCCTTTC[C/T]ATTGTGAGATAGCCA | 671564 |
rs242950428 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108755759 | TACCAATGCCTCAGG[A/G]ATCATTTGGAAGCCT | 671564 |
rs242972866 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108748921 | GCCTTCAATTTTAGG[C/T]AGGGCAGGGCTTTCT | 671564 |
rs243021936 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Rnf212 | Mm_Celera | 5:108728309 | ACTCATACAGATACT[C/T]ATATAAATGAAGTAA | 671564 |
rs243046851 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108754679 | GCAATGTGTAGTACA[C/G]TTGGATTCTATGCAA | 671564 |
rs243194381 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108738448 | GACAAATGGGAGGGC[C/T]ATGAGGTGGGAGTGT | 671564 |
rs243218071 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742713 | AGGTGTGATAGGCAC[G/T]CTGAAGAATAAGGAA | 671564 |
rs243326152 | snp | A/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764622 | TTTCTACATAGACTG[A/T]TGGCCAGTGTCTCCT | 671564 |
rs243332746 | in-del | -/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108739383 | GGCGCATAGGAAAAT[-/G]GAAGTTTATAAAGGT | 671564 |
rs243356694 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108746834 | TATCTATTAAAGGTC[C/T]TAGAAGTAACGCACA | 671564 |
rs243430227 | in-del | -/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108737796 | TGATGTCCCAGTGTA[-/G]GGGGAATGCCAGGAT | 671564 |
rs243436438 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108739062 | CCTCCAGCTGATAAA[C/T]ACCTTCAATTCAGTG | 671564 |
rs243529434 | in-del | -/TG | | | intron-variant | Rnf212 | Mm_Celera | 5:108732527 | TTTTAAAATTTAGTT[-/TG]TCTATTAATAAAAAC | 671564 |
rs243657348 | in-del | -/CAA | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108776436 | ATGGTCTCTTCACAT[-/CAA]TAGAACAGTGACTAA | 671564 |
rs243669028 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108739485 | GGGATTTTTATTGCT[A/G]GACTTTAATACTTTT | 671564 |
rs243730852 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108745360 | TGGAAGGAAAATGGA[A/G]CAGAAGCACGTGGCC | 671564 |
rs243765041 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108745883 | CAGCCCTATAGGCTG[A/G]GATAGAACAGGGCAG | 671564 |
rs243790782 | snp | C/T | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762497 | GTTGATTATATGCTA[C/T]TCATGATTTTAAAAA | 671564 |
rs243807936 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740369 | AATCCTGTACAATAA[G/T]AGAACTCCTGGAGGT | 671564 |
rs243879149 | in-del | -/CT | | | intron-variant | Rnf212 | Mm_Celera | 5:108758267 | ATAGACAAGTATAGA[-/CT]CTTTTGAGGTCATCC | 671564 |
rs244002414 | snp | A/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108752792 | GATGCCCATGGTGGT[A/T]TGAAGAGAGTACTGG | 671564 |
rs244124672 | snp | C/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108768597 | TACAACAGGTCGTCC[C/T]ACAGCCTGATCTTAT | 671564 |
rs244232242 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108769461 | GAGGATGTTCCTACC[C/T]TGCAGAGACTTGATG | 671564 |
rs244354058 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108734797 | AGGGAGCATTAGTCA[C/T]CAGGGAAATGCAAAT | 671564 |
rs244378633 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741043 | ATCTCAAATGGCTGA[G/T]AGATTATTACAGAAG | 671564 |
rs244404421 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108759862 | ATTTTACAAGTAAGA[C/T]AGTAAAAAAAAAAAA | 671564 |
rs244429000 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108750126 | CTAAGAATGAACATT[A/C]ATCAACAACTGTGAC | 671564 |
rs244517694 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108746387 | TGTAAAACCATGAAA[C/T]AAGACCTCAGATAGA | 671564 |
rs244628964 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108746769 | TGGATGGCTATTAGA[A/G]GAATGGTCTTCATTT | 671564 |
rs244732207 | snp | C/T | | | downstream-variant-500B, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108769300 | GGACCTAGGCTTCCT[C/T]CCCTAACACACAAAT | 671564 |
rs244774794 | snp | A/C | | | missense | Rnf212 | Mm_Celera | 5:108760016 | TCTAACTCACCTGAG[A/C]GGTCTCCTGGGAATA | 671564 |
rs244829330 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108748744 | CCTTCCAAAATCAGG[C/T]CTTAGGACTCTAATG | 671564 |
rs244953836 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108756970 | GGTCTACACAGTGAG[A/G]CCTTGTTGAGAGGGG | 671564 |
rs245032891 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108730742 | CTATCTTACCACAGG[A/T]GATTCAAACAGAGCC | 671564 |
rs245057217 | snp | A/C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108747757 | GAACAGGAACATTCC[A/C/T]TTACTGCTGTTAACA | 671564 |
rs245082214 | snp | G/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108748075 | AATATTCTCAATACA[G/T]ATATCTACTCTACAT | 671564 |
rs245119736 | in-del | -/A | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108740921 | ACCTGACAGAGGGCT[-/A]ATATCCAAAAGAAAT | 671564 |
rs245125362 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108772985 | gtgtgtgtgtgtgtg[A/T]gagagagagagagag | 671564 |
rs245167497 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108757561 | GCAGGGTTAAAGAGG[C/T]AGAAAGAGTTGAAAC | 671564 |
rs245227931 | snp | C/G | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775112 | AAGGCCGCGCCTTCC[C/G]GCCCAAACCGATACA | 671564 |
rs245346558 | snp | C/T | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108776021 | ATAAGATACAAAATA[C/T]CTTCTTTTTATTGAG | 671564 |
rs245462784 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108743715 | TGGCAAGAACCATAG[C/T]AATACCTATAATGTA | 671564 |
rs245569697 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108749760 | CAGCTAAAGGAGAAA[C/T]GGAGACAAGTAAATG | 671564 |
rs245706605 | in-del | -/ACAC | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108761261 | CATTACAACAAACTT[-/ACAC]ACACACACACACACA | 671564 |
rs245720336 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108730316 | ACAATTCTAGGCAGC[G/T]CTAGCACCTTCTCAC | 671564 |
rs245772568 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766847 | ACATGTTCAATCAGG[A/G]GTAGAATTGCTTGGT | 671564 |
rs245847804 | in-del | -/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108770311 | ATAAATGCATTTTAA[-/T]TTTCCTTAGCAAAAT | 671564 |
rs245872412 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766567 | TGTAAACTAGTAATG[A/G]TCCATTTTAATGACA | 671564 |
rs245906252 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108753070 | CATGCCTTCAGGCCA[A/C]CTTCAGGTGCTTGGT | 671564 |
rs245934507 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740028 | AATGCCCACCCAGGA[A/T]TTTAGCTTTTGACTG | 671564 |
rs246023851 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108761565 | GAAAAAGCTGTAGTA[G/T]GACACCACAACTTGC | 671564 |
rs246126686 | snp | C/T | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762640 | TGCTGCCTTATGAGA[C/T]GGGGCTACCACAGTT | 671564 |
rs246339665 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Rnf212 | Mm_Celera | 5:108728244 | CACCTCTAAGGGACC[C/T]GATGCCCTCTTCTAG | 671564 |
rs246621806 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108749632 | CTGGCCACCATGTAC[-/A]TAACTGGCACTTCTG | 671564 |
rs246630849 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108753849 | AAGTTGATCATGTGG[C/T]TCTTAGGCCTTTAAA | 671564 |
rs246700044 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108774595 | GCTTTGTACGCATGC[A/G]GCCCCCGGCTCTCTC | 671564 |
rs246713884 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744631 | CTGCTCCCTCAGTAC[C/T]AGGCTGTGCACTGTT | 671564 |
rs246745063 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108754134 | GAATTAAAAGGAATA[C/G]ACTAATTTGTTTGTG | 671564 |
rs246826450 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108761135 | GACAGTGATGCTGAG[A/G]GTGATTTGAACTGCG | 671564 |
rs246845055 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108754967 | TATTGGTCTTATTTT[C/T]CTTTGCTTTACCCTC | 671564 |
rs246906963 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108738126 | AGCACTTGCAGATAG[A/G]AGCCAGGTGTAGCTG | 671564 |
rs246936504 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108733561 | ACCTCTTTTCTCATC[A/C]ACATACACCACTCAC | 671564 |
rs246940502 | snp | C/T | | | downstream-variant-500B | Rnf212 | Mm_Celera | 5:108727842 | TGTCATAAATATTGG[C/T]TTTATAACATTTTAT | 671564 |
rs246992227 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108756847 | AACCTCCCAGGTGCT[A/G]GTAAACCCTATTCAG | 671564 |
rs247038224 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108771747 | ACACAAACACACACA[A/C]ACACACACACACACA | 671564 |
rs247103670 | snp | A/C | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767271 | GAGGAGCCCACATTT[A/C]TGGCTTGGGATGTGA | 671564 |
rs247203723 | snp | C/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108768071 | CTGTGAGCTCAAGGC[C/T]AGCCTGTTTTACCCA | 671564 |
rs247358851 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740399 | TACCACCATCCATGG[C/T]TTCAAGCTGTACTAC | 671564 |
rs247637298 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741987 | GTCCCACTTGCAAGC[A/T]ATGCTGTGGTAATGG | 671564 |
rs247674995 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108750351 | GCCTTTTGTTTTTTC[C/T]TTTTTCTTGGATATT | 671564 |
rs247712036 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108748374 | CTACTCTACATAATA[G/T]TCTCAATACATATAT | 671564 |
rs247727596 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108749542 | TTTGGAAATAGTTAA[C/T]TGCATGATTTTCTGC | 671564 |
rs247798863 | snp | A/G | | | synonymous-codon | Rnf212 | Mm_Celera | 5:108731706 | GCTGGGTGTCAAGCT[A/G]AGATGCTGGGGTCCC | 671564 |
rs247852269 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108758036 | CTGTTGTGGAAAGCA[A/G]TAACTCACCACAGAG | 671564 |
rs247964339 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108748488 | TGGTGGTAGCTCCCT[A/C]TGTGGCAGCTAGAGA | 671564 |
rs248044807 | in-del | -/CT | | | intron-variant | Rnf212 | Mm_Celera | 5:108771875 | GGTTCTGGGGATTAA[-/CT]ACTCAGGTTATCAGG | 671564 |
rs248073951 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108732166 | GTGATCAGTAAATAC[A/T]GGAGAGTCACATATG | 671564 |
rs248128644 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108731144 | AAGCAGCTGAAAGAG[A/G]AGGGCTTGCCTTAGG | 671564 |
rs248173015 | in-del | -/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108733962 | TCCAACCTATTGTGA[-/T]TTTTTTAATTAGGTA | 671564 |
rs248234468 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108772151 | TTTAATCCCAGCACT[C/T]CCAAGGCAGAGGCAG | 671564 |
rs248253470 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108746646 | CTTCATTCCCTGTTA[A/G]ACTCCTATTTACTCT | 671564 |
rs248475192 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108732715 | TAGTCTATGCCACTG[A/C]AGGTAATTTTTGCTG | 671564 |
rs248521250 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108769973 | GAACTAAAGGCACTG[G/T]TTTAAGCCCATGGAG | 671564 |
rs248559050 | snp | C/G | | | downstream-variant-500B, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108769168 | TGTGTTTCAGTTGGG[C/G]CAAGGATTGTAAGCC | 671564 |
rs248571610 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742185 | ATGAATGACATAATT[C/T]CTAATGATATTTTTC | 671564 |
rs248601588 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108741871 | TAGCAAAAACTCTTA[A/G]TAATGGGGGATACAG | 671564 |
rs248603136 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108730409 | CAAGGGCTACAGGTT[C/T]CATTCTTAGCATTCT | 671564 |
rs248647156 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741419 | AGAAAATATGGTACA[A/T]TTATATAATGGAGTA | 671564 |
rs248691108 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740523 | CCTATGAGTACCTGA[A/T]TTTTGATAAAGAAGC | 671564 |
rs248789976 | in-del | -/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108732762 | TGTTTTGTTCTTATT[-/C]CCTTTGATCTCTTTC | 671564 |
rs248934870 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108745125 | CCAACCAGTTGTTGT[A/G]GATTGCCCTGATGCT | 671564 |
rs248936446 | in-del | -/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108741601 | TACTCATGCTACAGT[-/C]CCACAGACCTAGAGA | 671564 |
rs248997681 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108732120 | AGTGGTTGGTCAGGG[-/A]AGGGCCAGCATGAAT | 671564 |
rs249004196 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108751846 | TCACTCAGGATGATA[C/T]CCTCCAGATCCATCC | 671564 |
rs249032791 | snp | G/T | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762868 | CATTCAATAATGAGC[G/T]TGTCCACACCAAGAC | 671564 |
rs249063503 | snp | C/T | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108776316 | AACTCTCAGCTACTG[C/T]TCCTGCCTGCATGCC | 671564 |
rs249129389 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744356 | TCTCAAAGATCAGCA[C/T]CAGTAGAGTTTCTCA | 671564 |
rs249157579 | snp | C/G | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775843 | AATTAGGAAAAAGTA[C/G]AGATTCAGGTGAATG | 671564 |
rs249373184 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108760928 | CACTGTCTCAAAAAA[C/T]CCAAAATCAATAAAT | 671564 |
rs249407537 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108774497 | ACAACAAAATGAAAC[C/T]GCAGTCTACAAGAAT | 671564 |
rs249515447 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108769675 | AAGATATTATTTGGG[-/A]AAAAAATCCATAAAA | 671564 |
rs249517029 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108742960 | GGAAGGGAGATAAAG[A/G]AAAAAAAAAGAGTCC | 671564 |
rs249520296 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108759400 | CACACACAAACATAC[A/G]CACACAGAGGGACAG | 671564 |
rs249540358 | in-del | -/CA | | | intron-variant | Rnf212 | Mm_Celera | 5:108739096 | GATACAAGATCAACT[-/CA]AAAAAAAAAAAAAAT | 671564 |
rs249596580 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108734538 | CATTCCATACATATA[C/T]TAATACAGAAACATG | 671564 |
rs249656280 | snp | C/T | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108776696 | AACTTACTCTGTAGA[C/T]TCACCTGGCCTTGAA | 671564 |
rs249679605 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108749501 | GAAATTGATTTCTCC[C/T]TCACTCATCCCAAAG | 671564 |
rs249692378 | snp | A/C | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775617 | GGTCATTCTCCCCCC[A/C]CCCCCCATTTAAAAC | 671564 |
rs249716304 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744477 | GTATGTACCTAGAGC[C/T]CAGAGACCTAATGCT | 671564 |
rs249810854 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108744005 | CTGCTCTGAGAACTC[A/G]GCCTTGTGCCCCCTA | 671564 |
rs249863523 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108737800 | GTCCCAGTGTAGGGG[A/G]AATGCCAGGATAGGG | 671564 |
rs249935565 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108729653 | TAGTTTTTTTCAGAG[C/T]ACCACTGACTAATGT | 671564 |
rs250054719 | snp | A/G | | | intron-variant, utr-variant-5-prime | Rnf212 | Mm_Celera | 5:108750726 | TTTCTCTAACTCCTC[A/G]AGCATCTGCCTTTGT | 671564 |
rs250076791 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108773227 | ATAAAAATAAGGAAA[A/G]ATTTAAGAAATTTGT | 671564 |
rs250139614 | snp | C/G | | | intron-variant, utr-variant-5-prime | Rnf212 | Mm_Celera | 5:108750693 | TGGGGTTACAAACCC[C/G]TTCAGCTCCTTCAGT | 671564 |
rs250204641 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108755097 | TCAGAAGAGACTCTA[A/C]ACTGATACTTTTGAA | 671564 |
rs250235497 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108742558 | TTTTTGTTTTTATCC[C/T]AGGTGTGGGATATGG | 671564 |
rs250293145 | in-del | -/TTT | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108765959 | GGCAACATCTGGTCC[-/TTT]TTTTTTTTTTTTTTC | 671564 |
rs250307150 | snp | A/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767411 | CCACAGAATAGTCAT[A/T]ATTAGCATGTATTAT | 671564 |
rs250454052 | snp | C/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766164 | CTCATTGATGTTTGA[C/T]GTACTTTTGCCTCTT | 671564 |
rs250459576 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108745855 | TAAAACCCCCTGCTC[-/A]CTGGATGATAGCCAG | 671564 |
rs250685698 | snp | A/G | | | downstream-variant-500B | Rnf212 | Mm_Celera | 5:108728015 | GTGAGTTTCAGGATA[A/G]CCAGGGCTATGGGAG | 671564 |
rs250692450 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108739870 | GAGCAGTCTGTTTGG[A/T]TGGAACCCCTGCTAA | 671564 |
rs250758039 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108753589 | GTGTGGTAGCATCCA[A/G]TGAGCTAAGAGGGTC | 671564 |
rs250764055 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108745864 | CCTGCTCCTGGATGA[C/T]AGCCAGCCCTATAGG | 671564 |
rs250840691 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740444 | AAAAACTGCGTGGTA[C/T]TGGCATGAAAAAGAC | 671564 |
rs250945224 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108746627 | CCTCCTCAAGGCATG[A/G]ATGCTTCATTCCCTG | 671564 |
rs251009643 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108745094 | GTACCTCTGCTGAGG[C/T]GAACCAAACTCTCAG | 671564 |
rs251015909 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108771717 | acacacacacacaca[A/C]acacacacacacaca | 671564 |
rs251082554 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108747213 | CAAGGGAAGGTGAAG[C/T]ATAGGGTTATGAGCC | 671564 |
rs251201478 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108755529 | GTACTGCTGTACCCT[C/T]AAATTGGGAGACAAA | 671564 |
rs251295675 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108737403 | TCCCACTTGGGGATC[C/T]ATTCCAAATTCAGTT | 671564 |
rs251300662 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741505 | TTAGAAAAAAGATCA[G/T]TTTGAGTGAAGTAAC | 671564 |
rs251347424 | in-del | -/AATG | | | intron-variant | Rnf212 | Mm_Celera | 5:108742157 | AATACAATTGGCCAA[-/AATG]AATGAATGAATGAAT | 671564 |
rs251362870 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108760383 | GACAGACAACAGAGT[C/T]TGTGAGGCGGTAAAG | 671564 |
rs251481973 | in-del | -/GATT | | | intron-variant | Rnf212 | Mm_Celera | 5:108754308 | TAGTTTAAAGTTATA[-/GATT]GACAAGGTGTGAGTG | 671564 |
rs251573450 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108742956 | GGTTGGAAGGGAGAT[-/A]AAGGAAAAAAAAAGA | 671564 |
rs251600766 | in-del | -/AAAAACAAAAACAAAAAC | | | downstream-variant-500B | Rnf212 | Mm_Celera | 5:108728041 | GGAGAGACTCCGTCT[-/AAAAACAAAAACAAAAAC]AAAAACAAAAACAAA | 671564 |
rs251632921 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108732915 | GCTATAAAATCCATG[C/G]TTACACAATAGCTAT | 671564 |
rs251804009 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741844 | ACTTCCTGAAATCTA[G/T]GAGAGTGATCCTAGC | 671564 |
rs251863517 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108744335 | GAAGTCAAGGGTTAT[-/A]AAAGCTCTCAAAGAT | 671564 |
rs251942194 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108749064 | CAAGCTTCACACTAA[C/T]GTAAGCTAAGTACCC | 671564 |
rs251983395 | snp | A/G | | | intron-variant, utr-variant-5-prime | Rnf212 | Mm_Celera | 5:108750681 | TTGTTCTTCCTTTGG[A/G]GTTACAAACCCGTTC | 671564 |
rs252018117 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108760790 | GGGAGAAAAAAAAAA[A/C]CAGTGGGTGTGGTGA | 671564 |
rs252026782 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108749874 | TCTAATATCCCTGCT[C/T]ACTGTCTGCTGCATG | 671564 |
rs252041169 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108757913 | AATGATATTTTAAGG[C/T]TCTATATATCCCTCT | 671564 |
rs252092781 | in-del | -/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108756982 | GAGGCCTTGTTGAGA[-/G]GGGGAGGGCGGGGAA | 671564 |
rs252280476 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108759780 | AGAGAAAGGCAAGTG[C/T]CACAGGAGCACAAAC | 671564 |
rs252310756 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740425 | ACTACAGAGCTATAG[C/T]AATAAAAACTGCGTG | 671564 |
rs252344640 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108732783 | GATCTCTTTCCTTGT[C/T]AGCTGTTGTTGGAGA | 671564 |
rs252400431 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108731652 | CTTGTGTTTTGCCCC[A/C]ATGGGGACTTACCTG | 671564 |
rs252435775 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108750534 | ATCGAGCCTTCACAT[A/G]ACCAAGATACCTCCC | 671564 |
rs252452186 | in-del | -/TA | | | intron-variant | Rnf212 | Mm_Celera | 5:108747519 | TTATAAACATCAGTT[-/TA]TAAACATCCCTGCAT | 671564 |
rs252458155 | snp | A/G | | | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728659 | CATACCACTGGAGTA[A/G]TCCAGTGGGCAGCCT | 671564 |
rs252465789 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108734701 | TAAAATAACCCTATT[-/A]AAAATGGGGTACAGA | 671564 |
rs252569741 | snp | C/T | | | nc-transcript-variant, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763924 | CCTTCTCCAACACCA[C/T]ATCTGCCTGTATGTT | 671564 |
rs252864980 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108739861 | TTTTACCAAGAGCAG[A/T]CTGTTTGGATGGAAC | 671564 |
rs252927170 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108755329 | GAGAGAATTTGTAGG[C/T]TGAATTAAATGAGGT | 671564 |
rs252952608 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108754433 | GCAAGACTTCCACCA[C/T]CAAAGGTTCCATTTT | 671564 |
rs253004862 | in-del | -/A | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762997 | GAAGAGATTTTAAAC[-/A]AAAAAATGAGCAAAG | 671564 |
rs253008779 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108744805 | GAACTGTGAGGAAAG[A/G]CAGTATGTTTTGAAC | 671564 |
rs253061474 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108745214 | AGGTGACTTCTTGTG[-/A]ACCTTTTCCCTATTT | 671564 |
rs253082304 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108745025 | AGACAGGAAAACAAG[A/G]GCAGTTTTTCCCATG | 671564 |
rs253111270 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Rnf212 | Mm_Celera | 5:108728117 | AACAAACCAATACCC[C/T]GCCCCTCAACTATAC | 671564 |
rs253141187 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108753731 | CCACTTCATAATGTG[A/G]ATAAAAATAAACTTA | 671564 |
rs253153004 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108738616 | TGCCCTCCCCCCCCC[A/C]AAAAAAAAGAAAAAA | 671564 |
rs253214560 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108745779 | CTGCCACTTGTGAGA[A/G]TCCAGTTCTATTTGT | 671564 |
rs253249142 | snp | A/C | | | utr-variant-5-prime | Rnf212 | Mm_Celera | 5:108775065 | CTTAGAAAGGCAGCT[A/C]TGCGCCTGCGTTCAT | 671564 |
rs253283400 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108737911 | ATAAAGTTTGCAATG[C/T]AAATAAAGAAAACAT | 671564 |
rs253400615 | snp | A/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108752724 | CTTTGAGTTGAGCTT[A/T]GTACAAGGATATAAG | 671564 |
rs253474152 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108733811 | GACAGAGTTCTCTCA[C/T]CTACTCAATCAGAGA | 671564 |
rs253635990 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108757990 | CTCCTTGGACCATAG[C/T]TGCATTAGCGTCTGT | 671564 |
rs253676011 | in-del | -/TT | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108733838 | GAGAGCAAAGAATCA[-/TT]TTTTTTTAGAGTTTA | 671564 |
rs253776437 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108771626 | TAAGCCCTGGACCTC[C/G]TTAGTACCCTATGTA | 671564 |
rs253943318 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108771715 | ACACACACACACACA[A/C]AAACACACACACACA | 671564 |
rs253960844 | in-del | -/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767658 | AAAATCAGTAAAAAA[-/T]AAACCACAATGAAAA | 671564 |
rs254008473 | in-del | -/TA | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767686 | AAATCCTGATTAACT[-/TA]AAAAAAAATACCCCA | 671564 |
rs254033557 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742136 | CAGAGGCCTAGGATA[G/T]AACCAAATACAATTG | 671564 |
rs254163069 | snp | C/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108768016 | AAATCTTTTTTTTTA[C/T]TAAAGATTAAATGCT | 671564 |
rs254218965 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108746837 | CTATTAAAGGTCCTA[A/G]AAGTAACGCACAATA | 671564 |
rs254267971 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108757213 | ACTTTAAGTGCGGGT[C/T]ACAGCATGTTCTACT | 671564 |
rs254317137 | in-del | -/AG | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763709 | AAAGAGAAGGGGAAA[-/AG]AGAGAGAGAGGGAGG | 671564 |
rs254361346 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108729348 | TCATCTCTCTAGAGT[A/G]AACTCTACCGTGATA | 671564 |
rs254391353 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767138 | GAGACTTATAAAGGT[A/G]AGATATCCCCTAGAC | 671564 |
rs254395052 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108730858 | ACACAATATACTACC[A/G]ACCAGGGGATACAAA | 671564 |
rs254466108 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108756089 | GTGGATCTAAGCTAG[C/T]CAGTAGGAGCCTAGA | 671564 |
rs254479367 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108740385 | AGAACTCCTGGAGGT[A/G]CCACCATCCATGGCT | 671564 |
rs254484520 | in-del | -/A | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108761509 | TATGAACATGGGTGC[-/A]AAAAAATCCCAAGAG | 671564 |
rs254530936 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108746048 | TGGCTGAATCCTGCT[C/T]AGGTCCCCTTTTCCC | 671564 |
rs254573151 | in-del | -/TATA | | | intron-variant | Rnf212 | Mm_Celera | 5:108749780 | CAAGTAAATGAGGGT[-/TATA]TATATTTTTTCCCCA | 671564 |
rs254588960 | snp | C/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766976 | CTGTGGGTGAGAGAC[C/T]ATAGCCATCTGAAAT | 671564 |
rs254596498 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108756608 | GAGTTTTAAAAAAAG[A/G]CTTTTATGTAAAAAA | 671564 |
rs254597204 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740639 | GATCCACATCTATCA[C/T]CCTGCACAAAACGCA | 671564 |
rs254622196 | in-del | -/G | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775851 | AAAAGTAGAGATTCA[-/G]GTGAATGTTTCTTAA | 671564 |
rs254638766 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767850 | CCTTTATTTCACTGT[A/G]GCCCAAGCTGATTTT | 671564 |
rs254667596 | snp | C/T | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775604 | TTACTTTAGGGAGGG[C/T]CATTCTCCCCCCACC | 671564 |
rs254680251 | snp | C/T | | | missense | Rnf212 | Mm_Celera | 5:108728969 | CAGGGCAGAACACAG[C/T]TCTGCAGAGATCTGT | 671564 |
rs254752705 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108745452 | TCTGCCCAATCTAGG[C/T]GCACAGCTTGTATTC | 671564 |
rs254815530 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108754123 | TCAGTGAGGCTGAAT[G/T]AAAAGGAATAGACTA | 671564 |
rs254833744 | in-del | -/A | | | downstream-variant-500B, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108769067 | AAACAAAAAACCAGG[-/A]AAAAAAAAACCCTCA | 671564 |
rs254885756 | snp | A/T | | | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728534 | CCATGCCTGGGTCAT[A/T]TACACTTCCTGGGAC | 671564 |
rs255269660 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108774621 | CTCTCCCCCCACCCC[C/T]CAGGCTTTACTTCAA | 671564 |
rs255460077 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108754092 | ATGGCTGTATTCTAG[C/T]TATGTTCTAAGAACT | 671564 |
rs255529181 | snp | C/T | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762351 | ACCTGTAACTCCTAC[C/T]CCAGGGAATCCAATT | 671564 |
rs255531658 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108759666 | TGGAACTTTGGGCTC[A/G]GCATAGGGGACACTG | 671564 |
rs255658845 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108749846 | CAGAGACAACCTTGT[C/T]TGAGGTCTTATGTCT | 671564 |
rs255663150 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108749931 | CACCCTGGCTGCCCC[A/C]ACCTGCTTGACCTAG | 671564 |
rs255727890 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108749460 | TCATACTAAATAGAT[A/G]GAATAAAGGTAGTAG | 671564 |
rs255744972 | in-del | -/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108773825 | ATTCCTGACTCTTTT[-/G]AATTCCAGATTTCCC | 671564 |
rs255745632 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108773090 | ACCTGAGTTCAACTC[C/T]CAGGATCCATATGGT | 671564 |
rs255813359 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108743079 | ATTTCATGGATGCCT[C/T]GTAGAAAATATATGG | 671564 |
rs255822335 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108734378 | CTGGGTCCTTTCAGC[A/T]AAATCTTGCTAGTGT | 671564 |
rs255941085 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108732867 | TTTCTATACGACCAC[A/C]ATAACTAGAACCCTT | 671564 |
rs255963214 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108770878 | TCACCCCACATCCAG[A/G]GCATTCAGGTATGAG | 671564 |
rs255984055 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108747798 | GCCCACACATTACAG[A/C]ATTCATTAGTCAAAA | 671564 |
rs256061397 | in-del | -/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764757 | ATTGTTGGAGGCTAC[-/T]TTTTTTTTCTCCATT | 671564 |
rs256137585 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108759604 | AGGACAACTTCCCTT[C/G]ATGTTGAGTATATTG | 671564 |
rs256153970 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108755641 | GTCTTGAAGAACACA[C/T]GCCATGTCAAGCTCA | 671564 |
rs256187051 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108742552 | AATATGTTTTTGTTT[A/T]TATCCTAGGTGTGGG | 671564 |
rs256497712 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108771884 | GGATTAAACTCAGGT[C/T]ATCAGGCTCAGCAGC | 671564 |
rs256679881 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Rnf212 | Mm_Celera | 5:108728249 | CTAAGGGACCCGATG[C/T]CCTCTTCTAGACTTG | 671564 |
rs256728683 | in-del | -/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108753885 | TTTTAGGGAGAATGT[-/G]GAAGAGTCTAGAATT | 671564 |
rs256728811 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108732467 | TCCTATTATAGTAAG[C/T]ATTTGGCATTATAAA | 671564 |
rs256730706 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108753862 | GGCTCTTAGGCCTTT[A/G]AAACCAGTTTTTAGG | 671564 |
rs256853882 | snp | C/G | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108768423 | GTTAGGGCAGGAACT[C/G]AAATAGGCAGGAATC | 671564 |
rs256969270 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764647 | TCTCCTCAGGAATCC[A/G]CCAGGACTATAGAAT | 671564 |
rs257071262 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108739119 | AAAAAAATCAGTAGA[C/T]CTCCTGTACACAAAT | 671564 |
rs257111288 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108754064 | GAGGTCATTTGTGTT[A/G]TGTTCTGGCAAAATG | 671564 |
rs257146314 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108729607 | GAGTTCACTGATTTA[A/C]GTATGTGTTTTTAAA | 671564 |
rs257169712 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108745965 | TTGGGGACTCCACTA[A/C]ATTCTGTTAGAATTA | 671564 |
rs257236428 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108754468 | AAGTCAACTACGTCC[G/T]AGGGAAGAGTTTCCT | 671564 |
rs257236648 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108745255 | AATAAAGGTTAGAGC[C/T]GGTGATTGGGCAATG | 671564 |
rs257315546 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108760856 | GCAGGCAGATCTCTG[A/T]GACTTTGAAGCTGGG | 671564 |
rs257322143 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108738201 | TACAGCCAACCATTA[G/T]ACTGAACATGGGGGC | 671564 |
rs257483045 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740952 | AAAGAACTCAAGAAA[C/T]TAGACATCAACAAAT | 671564 |
rs257566906 | snp | A/C | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108765822 | GTTGTACAAGCCTGC[A/C]ATCCCACCAACAATG | 671564 |
rs257570270 | in-del | -/AGAGAA | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108739309 | AGAGGAGGGAACCAG[-/AGAGAA]GGAGGAGGGGTATTT | 671564 |
rs257829139 | in-del | -/CAGAAGTAGCACCAGGT | | | nc-transcript-variant, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767047 | GGAGTTATCCTGCTA[-/CAGAAGTAGCACCAGGT]CAGAGATGCTGACCT | 671564 |
rs257911163 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108739419 | GGGAAACCCAATGTT[A/T]GTATGAGGTGTTTAA | 671564 |
rs257965952 | in-del | -/TT | | | downstream-variant-500B, upstream-variant-2KB | Tmed11, Rnf212 | GRCm38.p3 | 5:108776824 | CCTTTTGTAAGATCC[-/TT]TTTTTTTTTTTCAAT | 671564 |
rs258277267 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108740595 | GGTGCTGGTCTATCT[C/G]GATGTTAGCACATAG | 671564 |
rs258368824 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108747370 | AACAGCTTTGCTAGA[C/G]ACCACAATGTGCCTT | 671564 |
rs258429482 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108746726 | GACATAACTCCTGAT[A/G]AACAAGTGCACACGT | 671564 |
rs258476693 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108749222 | TACAAATTCTTACAC[A/C]ATCCCACCAGGCCCA | 671564 |
rs258535635 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108758673 | CTAACTGCCTGCCTC[C/T]TGCCTCCTGCCTTCT | 671564 |
rs258544589 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108748602 | GGAACCCACACCAGC[C/T]TGCTGCAGACCCATA | 671564 |
rs258550578 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764547 | TTTGCATCCTGGAAA[A/G]TTCATCTATTATGTT | 671564 |
rs258627629 | in-del | -/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108768006 | TTGCTTTTTAAAATC[-/T]TTTTTTTTATTAAAG | 671564 |
rs258722918 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108774002 | GACTCTAACCCTGAA[A/G]TAGCAACAAAAATAA | 671564 |
rs258792475 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108729531 | TTGACATGACTTCTA[C/T]ACTGCTGAAGAAAAC | 671564 |
rs258814073 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108742697 | ATGCCAAGGCCTCCA[A/G]AGGTGTGATAGGCAC | 671564 |
rs258965348 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108733190 | CACACACACAGCAAA[A/G]CACACTGGGAATACA | 671564 |
rs258969584 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108730572 | AACTTTTCTCTTGCC[A/T]ATGCATTCTAGATGA | 671564 |
rs259003528 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108738912 | ATTCAATATAGTACT[C/T]GAAGTTCTAGTTAGA | 671564 |
rs259024793 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108769835 | TGTTGTATTTTTTTT[-/A]AAATTGTGATGTTTA | 671564 |
rs259113411 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108769511 | CCAGGTGAAGGGTCT[C/T]TACCCTCTCAGAGGA | 671564 |
rs259221681 | in-del | -/CAGGG | | | intron-variant | Rnf212 | Mm_Celera | 5:108745891 | TAGGCTGAGATAGAA[-/CAGGG]CAGGGCAGGGCAAAG | 671564 |
rs259252271 | snp | A/G | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762482 | AATCAATATAGTTAT[A/G]TTGATTATATGCTAT | 671564 |
rs259372302 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108734764 | AATGGCTGAGGAGCA[C/T]CTAAAAAAATGTTCA | 671564 |
rs259457439 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108747583 | TCTTGGGGTTGTTAG[A/G]GTGTGGTTGGTTATA | 671564 |
rs259593393 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108750415 | CCAGGTCCCCCAAGC[C/T]CTCAGAAACCCCCAT | 671564 |