SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3663149 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116257911 | CCATAATTATTACAG[A/G]GCCCATTCATTTGGC | 217935 |
rs3663667 | snp | A/T | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116257954 | TACTATTACCAAATT[A/T]AAAAAAAAAGCAAAG | 217935 |
rs3663683 | snp | A/G | 0.5 | 0 | intron-variant | Wdr60 | GRCm38.p3 | 12:116257960 | TACCAAATTTAAAAA[A/G]AAAGCAAAGTTACAA | 217935 |
rs3663714 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116257981 | AAAGTTACAATGGCA[C/G]ATAAGTACCAGAGCA | 217935 |
rs3664943 | snp | C/T | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116258199 | AAAAAGGCAAGTATG[C/T]GGTACACAGACAACA | 217935 |
rs3689311 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Wdr60 | Mm_Celera | 12:116217238 | AAAGGGCAGCTTCAA[A/G]CGTACTGCAAGACCT | 217935 |
rs6160755 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116257896 | ACTCACTAAAGTAAT[C/T]CATAATTATTACAGG | 217935 |
rs6200816 | snp | C/T | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116225912 | AATCTGTTATCTCTG[C/T]CCCTCCTTGTGGGAC | 217935 |
rs6214666 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Wdr60 | Mm_Celera | 12:116226204 | TACCCACATAAAATC[C/T]AACTCAATGAGGAAG | 217935 |
rs6215249 | snp | C/T | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116226328 | CACGCTAGGAAAGCA[C/T]TATACCCAATGAGCT | 217935 |
rs6215306 | snp | A/G | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116226363 | CCTCAATCCCCAAAC[A/G]CCAGTCTTCCTCCAC | 217935 |
rs6215346 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Wdr60 | Mm_Celera | 12:116226386 | TCCTCCACGCCTACA[G/T]CCTAAACCTAAATTC | 217935 |
rs30531247 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Wdr60 | Mm_Celera | 12:116243503 | ACAAGAATGATACAC[C/T]AGAATAAGAAAAGTA | 217935 |
rs30533450 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Wdr60 | Mm_Celera | 12:116227717 | AACTTCCCAATGTTT[C/T]CTTGGTCACTTTTTC | 217935 |
rs30533877 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116243052 | GAGCAGGGGAAGAAG[C/T]TCACTACGGAGGAAG | 217935 |
rs30538800 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116209180 | AAGGTATAAAGGCGG[A/G]GATATGGGAGATAGT | 217935 |
rs30564574 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116211669 | GTGGTGTTAAATGTA[A/C]TTTTGAACCTGTAAT | 217935 |
rs30567828 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Wdr60 | Mm_Celera | 12:116215519 | ACACATCATTCTCAT[A/C]ACTACACACAGAAGG | 217935 |
rs30569603 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Wdr60 | Mm_Celera | 12:116219137 | GGAAAAACAAGAAAT[G/T]AATACCAAGGCTTGT | 217935 |
rs30573299 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr60 | Mm_Celera | 12:116259774 | AAGACAATACACCTT[C/T]TCCAGAAGCCAGCAA | 217935 |
rs30574214 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116255247 | CCAAAGGTAAAGTAT[A/C]CACGAAAACCTCAGA | 217935 |
rs30574838 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116206654 | GGTGCTGAGCCATCA[C/T]GAGCAGATTGGTTAG | 217935 |
rs30578027 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116241163 | TTGTTGGGTCATGGA[A/C]GCTTCTACCTATATT | 217935 |
rs30579504 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Wdr60 | Mm_Celera | 12:116211717 | GAGGGTGACTGGCCT[A/G]TACTCACTTATCTGG | 217935 |
rs30583880 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116243106 | AACTGCGATGAAGTC[A/G]GACTCTTCTGAAAGA | 217935 |
rs30584507 | snp | C/G | 0.401235 | 0.199068 | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116206451 | TATCCAGGCCCAAGA[C/G]ATTGCAGTTCTCGCT | 217935 |
rs30584759 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116224818 | GCATAATCTGAATGA[A/G]TAAAAGCAGATAAAG | 217935 |
rs30589381 | snp | A/T | 0.465374 | 0.126941 | intron-variant | Wdr60 | Mm_Celera | 12:116241192 | TTTTAAGAGATCAGT[A/T]CCACAGAGCGACAGT | 217935 |
rs30603577 | snp | A/T | 0.46875 | 0.121031 | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235285 | AACCTTGTATCCCTA[A/T]TTCTTAGGTGTTACC | 217935 |
rs30615269 | snp | A/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116211670 | TGGTGTTAAATGTAC[A/T]TTTGAACCTGTAATT | 217935 |
rs30618805 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr60 | Mm_Celera | 12:116209511 | CCTATATAACTCACT[A/G]AACTTGTAGAAGTCA | 217935 |
rs30623390 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Wdr60 | Mm_Celera | 12:116243612 | GAACAAACAAATCAA[A/T]GTGTAGGTATGTGTC | 217935 |
rs30626731 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr60 | Mm_Celera | 12:116209625 | ATATAAACACTAGCC[C/T]AGCTATAAACCTTGC | 217935 |
rs30627248 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116244651 | CACAACTGAATAATT[A/G]TGTGTATCAGGTTTA | 217935 |
rs30631415 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Wdr60 | Mm_Celera | 12:116227961 | CAAATGAATGAATAA[A/G]CAGGCCGATGCTGGC | 217935 |
rs30632538 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116219277 | TCCAGAAAGAGAGGA[C/T]ATGATTCTGGGGCCA | 217935 |
rs30637869 | snp | A/G | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116208693 | GTTCATATGTGACCA[A/G]CAGCTAGAGTGAGTG | 217935 |
rs30639728 | snp | A/C | 0.32 | 0.24 | intron-variant | Wdr60 | Mm_Celera | 12:116217763 | ATCCAAAGCCACAGA[A/C]GAAAACTCCAAATGC | 217935 |
rs30649731 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116224493 | AGACAAGGTCTCTTG[C/T]TGGGCCTAGAGCAGT | 217935 |
rs30651812 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116257398 | TCATGTGACTCCCAC[A/G]CCAAGTCTTTAAAAT | 217935 |
rs30668069 | snp | A/C | 0.32 | 0.24 | intron-variant | Wdr60 | GRCm38.p3 | 12:116209626 | TATAAACACTAGCCC[A/C]GCTATAAACCTTGCA | 217935 |
rs30670202 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Wdr60 | Mm_Celera | 12:116234019 | ACCCTAAAGGCGATG[A/G]CACTGGATTCAATGT | 217935 |
rs30671608 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr60 | Mm_Celera | 12:116259769 | ACCACAAGACAATAC[A/G]CCTTCTCCAGAAGCC | 217935 |
rs30674060 | snp | C/T | 0.432133 | 0.171253 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116207042 | CAATTAGTAAGCCCC[C/T]ATTATTCCATTCTCA | 217935 |
rs30674756 | snp | C/G | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116215339 | ATGGGCTTCTATAAT[C/G]TCAGAGCCCAACCAT | 217935 |
rs30676373 | snp | G/T | 0.432133 | 0.171253 | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116207064 | CCATTCTCAAAAAAT[G/T]TATTTACTTGTATTA | 217935 |
rs30676847 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116215631 | GGCAGAAGAGAAGAC[A/G]AAGACCTGGTATGTC | 217935 |
rs30677732 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr60 | Mm_Celera | 12:116209414 | GGGGCTCCATAGAAA[C/T]CCCCAAACAATCCAG | 217935 |
rs30677869 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116263379 | ACTTAGGAAGTATCT[A/G]GATCGTATGTTAGCA | 217935 |
rs30681276 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116215706 | TAAGTTAGGACTCTT[C/G]TTATAATCCAGTCTG | 217935 |
rs30682278 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116208862 | TGTTGATATAGTTTT[G/T]GTTTCCTTTTCTTTT | 217935 |
rs30686874 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116219596 | ATTCTCCCACTGCCC[A/C]ACCCCATCCCCGAGA | 217935 |
rs30687105 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Wdr60 | Mm_Celera | 12:116228055 | TATCACTGTATCTGA[C/G]CAGAGATTGGGACAT | 217935 |
rs30712710 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Wdr60 | Mm_Celera | 12:116219355 | GAAAGTGCTGCTCAC[A/G]GGCAACTGATAAGGG | 217935 |
rs30713211 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Wdr60 | Mm_Celera | 12:116244426 | GCCTAGCACTCATGC[A/T]TGTGGGTTCATTATA | 217935 |
rs30718044 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Wdr60 | Mm_Celera | 12:116228093 | ATGAAATTCTAACTG[C/T]GCACTGTGAGCCTAT | 217935 |
rs30719254 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116221121 | ACCAGAAAACAAGAA[C/T]TTTAAGATGGGACAA | 217935 |
rs30719516 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116215206 | CTTACAGTTTTAAAA[G/T]ATTAGTGCATGATCA | 217935 |
rs30719603 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116224804 | TGATCTCTTCCTCTG[C/G]ATAATCTGAATGAGT | 217935 |
rs30722643 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Wdr60 | Mm_Celera | 12:116216845 | AGTTAAAATGCCAAA[C/T]CCAGTGCTGTAGATA | 217935 |
rs30725737 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116254595 | TTTACTGTTATTGCA[C/T]GTATGTTCATTAATT | 217935 |
rs30728282 | snp | A/C | 0.465374 | 0.126941 | intron-variant | Wdr60 | Mm_Celera | 12:116244223 | CTTTTTCAAGCACTA[A/C]GGATGACTCTGACGC | 217935 |
rs30730659 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr60 | Mm_Celera | 12:116217768 | AAGCCACAGAAGAAA[A/G]CTCCAAATGCAGGAG | 217935 |
rs30735481 | snp | A/G | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116221997 | TAATCCCAGGACTCA[A/G]GAAGCAGAGGCAGGC | 217935 |
rs30762614 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116243259 | GCATAATCAGAGGAC[C/G]GTAAACTATTCTAAC | 217935 |
rs30768197 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Wdr60 | Mm_Celera | 12:116216990 | TCTGCTCCAACATCA[C/T]AGCACTCCAGCTCCC | 217935 |
rs30773323 | snp | C/T | 0.5 | 0 | intron-variant, missense, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116262645 | TGACACTCAGCCTCG[C/T]CTCTGGATGAGTCCA | 217935 |
rs30773367 | snp | C/T | 0.415225 | 0.187619 | downstream-variant-500B | Wdr60 | GRCm38.p3 | 12:116205845 | GGAGATTCCAGTCCT[C/T]TGTTTAGCACGGGTT | 217935 |
rs30776453 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116244468 | ATGTAATTAACAATC[C/G]AGGGAGGTCTTACCC | 217935 |
rs30778747 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116254669 | CAAGGGCAACAAGTG[C/T]CAGGATCTAAACTTA | 217935 |
rs30779622 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116224823 | ATCTGAATGAGTAAA[A/T]GCAGATAAAGATAAA | 217935 |
rs30781360 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116243018 | AACTGTTCAGATAGC[A/G]CTTAGGCCACGCAGG | 217935 |
rs30817483 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235144 | ATAAAAATATTCTTA[C/T]TAGGTGAAATTCCAC | 217935 |
rs30817509 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116208913 | AGCCCAAGTTGATCA[A/G]GAATCCCCTATAAGC | 217935 |
rs30818296 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Wdr60 | Mm_Celera | 12:116239398 | ATTCCTTTATACAGA[A/G]CAGAGCAGAAGGTCC | 217935 |
rs30819294 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116259681 | AAAAGCTAGAGCAGA[C/T]ATCTACACCAAGAAA | 217935 |
rs30820534 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116257205 | TCAAACTGATGGGAC[G/T]ACCAGACTGGGTTAC | 217935 |
rs30820871 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116206546 | CAGGCAGTTTTCCCA[C/T]GAGCTCACCCTCAGA | 217935 |
rs30822245 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116243016 | TTAACTGTTCAGATA[A/G]CGCTTAGGCCACGCA | 217935 |
rs30826707 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Wdr60 | Mm_Celera | 12:116231913 | CAACTTCACACTGCT[C/T]TACAGGAAGTTCAGA | 217935 |
rs30829635 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116258561 | AGTGGCCAGAATGTG[A/T]GGCAGTCCACCCAAT | 217935 |
rs30830180 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116244762 | TCCCAAGCTAGTAGT[C/T]CTGGGCTAGCTAAGG | 217935 |
rs30850716 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116241157 | CAAGAATTGTTGGGT[C/T]ATGGAAGCTTCTACC | 217935 |
rs30855132 | snp | A/C | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116209109 | AATATAACCTTTACA[A/C]TCTATCAAACATTTC | 217935 |
rs30862457 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116259868 | GGAATTGCAAATATG[C/T]TCAAGGTCCTTAAAG | 217935 |
rs30865240 | snp | A/G | 0.401235 | 0.199068 | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116206495 | AAGAGCTTTAAATAC[A/G]CTGCTTGTGTTCCCT | 217935 |
rs30866235 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116215997 | GCTGTATATGTAGAT[A/G]AGGATGGCCTAGTTG | 217935 |
rs30868310 | snp | C/T | 0.432133 | 0.171253 | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116211799 | GACATAGATCCTAGA[C/T]GCATCGTCCTGGACC | 217935 |
rs30870948 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Wdr60 | Mm_Celera | 12:116244369 | AAGCAGGATACAGTT[C/T]GCTACAAATGTGGTG | 217935 |
rs30871767 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116206412 | CCCATGGATCAGAGG[C/T]AGACAGCAGAGTTTT | 217935 |
rs30872524 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116244668 | GTGTATCAGGTTTAT[C/T]AGTGGACATGTCTGT | 217935 |
rs30872569 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Wdr60 | Mm_Celera | 12:116231995 | GTTTGGTGTGAGTTT[C/T]AGGTTACAGATCAAG | 217935 |
rs30874447 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | GRCm38.p3 | 12:116238853 | ATAGGTCTGTAAGCA[A/G]AGAATTCTCATGGTT | 217935 |
rs30878134 | snp | A/C/G | 0.375 | 0.216506 | intron-variant | Wdr60 | GRCm38.p3 | 12:116254508 | CTTGCTAAAAAAAAA[A/C/G]CACAACAGCATATTT | 217935 |
rs30878561 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116217027 | GGCTTTACTTCCCAT[C/T]CCTTCCCTTGCTCTT | 217935 |
rs30878597 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116221802 | CCCCATTTAGCATGC[A/C]TCCAGGATTATCTCA | 217935 |
rs30879831 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Wdr60 | Mm_Celera | 12:116229333 | ATCTCAGTTTCCACT[C/T]ACTAAATAAGTTCAC | 217935 |
rs30880849 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Wdr60 | Mm_Celera | 12:116217733 | ACACTTAGCGCACTC[A/G]TGTGCACTGAGTAAA | 217935 |
rs30898332 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116242717 | CCTGCAAAAGTTTCC[A/G]CACTGTTGCATGATG | 217935 |
rs30908482 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116258661 | TAAGCAGCCTGAGGG[A/G]TATGTGTTCTCCAAT | 217935 |
rs30913987 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116259441 | GTTGGGACAGAATAA[A/G]GGTCCCCCTAGTTCC | 217935 |
rs30917758 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Wdr60 | Mm_Celera | 12:116220881 | ATACTCTCCATAGCA[A/G]CAGTATCTCCCCAAA | 217935 |
rs30919984 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116244794 | AGCTAGTTAAGCATG[A/G]GCCTGGTGATGAGTC | 217935 |
rs30920132 | snp | A/G | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116221963 | AAACTGATAAACTGG[A/G]CAGTGATGGTGCATG | 217935 |
rs30927642 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Wdr60 | Mm_Celera | 12:116244395 | TGGTGATTAAACAGT[A/G]GTCATGGCCAACACC | 217935 |
rs30943625 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116224826 | TGAATGAGTAAAAGC[A/T]GATAAAGATAAACCT | 217935 |
rs30953744 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Wdr60 | Mm_Celera | 12:116233967 | TAGGTGTCCTCTTGC[C/T]TCACAGTCTTCTTTC | 217935 |
rs30957960 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr60 | GRCm38.p3 | 12:116216202 | GAAAATATCTAATAA[A/T]AAAAAAAAAAGAGCC | 217935 |
rs30959597 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116243097 | CAAATCTTCAACTGC[A/G]ATGAAGTCAGACTCT | 217935 |
rs30960643 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116208834 | GTGATGGGCATGAGC[C/T]GCCATGCTCAGATGT | 217935 |
rs30960734 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116243291 | GAGCCAAGTCCCCGC[C/G]CAGCCAGCTTTGGTT | 217935 |
rs30960759 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116224575 | TAGTGACCTCTGATC[A/G]TAAATTTATTTTTGT | 217935 |
rs30973207 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116244669 | TGTATCAGGTTTATC[A/G]GTGGACATGTCTGTG | 217935 |
rs30975098 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Wdr60 | Mm_Celera | 12:116243780 | TTCCTGGTTTTACTT[A/G]TCAACACATTTAATT | 217935 |
rs30999003 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Wdr60 | Mm_Celera | 12:116229477 | ATTTTATAGAAAATA[A/G]ATCCCATCACATTTA | 217935 |
rs31001730 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Wdr60 | Mm_Celera | 12:116227881 | TCCCAAAGTGAAGGA[C/T]TTCTGTCTTACCTAC | 217935 |
rs31010454 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235427 | GCTAGACATCCAAAC[A/G]ACTTATCATTTCATT | 217935 |
rs31012361 | snp | C/T | 0.5 | 0 | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116256030 | TTTCTCACGGTCTTT[C/T]GCATCTTTCCTCCTT | 217935 |
rs31018102 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116224764 | ATCACAGTGTGTACT[A/G]CAAATGCCTCTTTTG | 217935 |
rs31020019 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116253654 | CCTATAGGAGGAACA[A/G]CAATATGAACTAACC | 217935 |
rs31021875 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116225213 | CTGCCCAAGTGTGAG[C/T]TTCTTCACACAGACA | 217935 |
rs31022412 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Wdr60 | Mm_Celera | 12:116232031 | AAAGATGAGAAATCT[A/G]CAACACCTAGGGTGC | 217935 |
rs31022472 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235271 | ATTAATGTTAACCCA[A/G]CCTTGTATCCCTATT | 217935 |
rs31022636 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Wdr60 | Mm_Celera | 12:116215096 | CTTTTAAGGACCAAG[C/T]CCAGTTATTACGTCT | 217935 |
rs31022931 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116263692 | CTGGTTCTTGCCTAT[A/G]GCCATTTCTGCCTCA | 217935 |
rs31026053 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116243465 | GTTTTGGGGGAAACG[A/G]GGTAGGTGGTGTGTG | 217935 |
rs31027631 | snp | A/G | 0.401235 | 0.199068 | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235198 | ACTACACTAAGTGTT[A/G]ACTATGTTATTGTTG | 217935 |
rs33864615 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr60 | Mm_Celera | 12:116254104 | ATGGACTACAATGTG[A/G]AAATGTAAGCCAAAT | 217935 |
rs33864915 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116242860 | CTGGTTTGGTTCCCA[A/G]CACTCATGTGGCAGC | 217935 |
rs33866229 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116243270 | GGACGGTAAACTATT[C/T]TAACTGAGCCAAGTC | 217935 |
rs33866546 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116259317 | TATGTATAGCCCTTT[C/T]TCCCTTCCTGTCATC | 217935 |
rs33866619 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116257565 | GCTTAGGCAGGAAGA[C/T]TCTAAATTCCAAGCC | 217935 |
rs33866944 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116209251 | TATAGTGAAAACTTT[A/T]AAAAAAAACATGTAC | 217935 |
rs33900036 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Wdr60 | Mm_Celera | 12:116220201 | ACGTCATACGCAGTC[A/T]TCTAGAAATGATGTC | 217935 |
rs45649078 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116246641 | AAATAATTACTACAT[A/C]TGCACTAATTTTTAA | 217935 |
rs45683877 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116226221 | ACTCAATGAGGAAGA[A/G]CACATGGGTTGTTCA | 217935 |
rs45686372 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116211555 | TGCACAACTGGGGGG[A/T]GGGGGTCCAAGTACA | 217935 |
rs45723690 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116210836 | ATATGGTTATAAAAT[A/G]CCAAGAACAAAATAT | 217935 |
rs45727778 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116211203 | CACAGTGGGAAGGGT[A/G]CGTGGGGACTGGTGA | 217935 |
rs45735424 | snp | A/T | 0.32 | 0.24 | intron-variant | Wdr60 | GRCm38.p3 | 12:116230334 | TGAAAAGACTTAAGA[A/T]TTAGCAGAAATGGGG | 217935 |
rs45749550 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116229291 | ACTACCTGAGAGAAA[C/T]TATAGGACTTAAAAC | 217935 |
rs45752213 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116245587 | TAACTTGATTCATTG[A/T]GGACTACAAGATCTT | 217935 |
rs45753632 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116240882 | GCAGAATCCACTTTA[A/G]TCATTTGAAAGCCTG | 217935 |
rs45758519 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116207207 | GAAGGCTGATGGAGG[C/T]CACCTCCAAAGTGAG | 217935 |
rs45761958 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116259848 | AAGACAGGGGTTTCA[A/G]AAGAGGAATTGCAAA | 217935 |
rs45769642 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116229904 | TGTATAAGCAGGCAA[C/T]ATCCATACACATAAA | 217935 |
rs45783719 | snp | A/G | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116216231 | CCAGGCAGTGGTGGC[A/G]CACACCTTTAATCCC | 217935 |
rs45801238 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116222888 | TGATGCCCTCTTATG[A/G]AGTGTCTGAAGTCAG | 217935 |
rs45817158 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116231027 | GACTTCCTCATGCTG[C/T]TGTATCCCTCCTACC | 217935 |
rs45851311 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264960 | CTCAAGACCTTGGCT[A/G]TATCTGATGCCCTGT | 217935 |
rs45857969 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116213365 | TTAACCAAAAAGTGA[C/T]TTTCTTACCAAGAAT | 217935 |
rs45864558 | snp | A/T | 0.444444 | 0.157135 | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116207269 | ATTTTATGCATGGCT[A/T]AAAAAATAGTCCATT | 217935 |
rs45868458 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116247869 | TAAGGCTGATGCTTC[A/G]TCATGGCAACCAAAA | 217935 |
rs45868761 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116246360 | TTTTAATGTTGCTGG[A/T]CTGTAAATCTATAAT | 217935 |
rs45892214 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Wdr60 | GRCm38.p3 | 12:116250214 | TGACATGTGCTGCCA[G/T]TGTGTATTACAGTGA | 217935 |
rs45897390 | snp | A/C | 0.495868 | 0.0452663 | intron-variant | Wdr60 | Mm_Celera | 12:116211988 | ATTGTTCTTTCTTTT[A/C]ATTTCCATCCTAACA | 217935 |
rs45912095 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Wdr60 | Mm_Celera | 12:116211622 | CTAAAACTACTGTTA[A/G]AAACATTTTTGACTA | 217935 |
rs45915563 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264404 | ACATTCCTGTGTTGG[C/T]CCAGCACCACTTTCC | 217935 |
rs45919209 | snp | C/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116245369 | ATAGTACAATCCACA[C/T]AGTAAAAAGACTGGG | 217935 |
rs45927221 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116226857 | TCCTTCCGCATCGCC[C/T]CACCCACTCACAGCC | 217935 |
rs45949135 | snp | A/G | 0.473373 | 0.11227 | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264462 | TATGTACTTGTTGCT[A/G]TCCTCCGTTCTCTTT | 217935 |
rs45992007 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116223585 | AGAAGAGTGGCAGTG[G/T]ACACACATACAACAC | 217935 |
rs46012428 | snp | C/G | | | downstream-variant-500B | Wdr60 | Mm_Celera | 12:116206008 | GCTCCTTGTGACTCA[C/G]TGGCCAGTATGACAG | 217935 |
rs46049952 | snp | C/T | 0.459184 | 0.136902 | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264545 | ATTTATAATTTCACA[C/T]TATTATGGATACAAA | 217935 |
rs46059622 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116245042 | ACTCCATGAGCACCA[C/T]TAAACAACTTCTGAG | 217935 |
rs46064559 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116241907 | ATTGATAAATCACAC[C/T]AGTAAGAACTTTAGA | 217935 |
rs46067771 | snp | A/G | | | intron-variant, upstream-variant-2KB | Wdr60 | GRCm38.p3 | 12:116234950 | ATCTTAGTTTTACAT[A/G]TAGATTTTAAAATTC | 217935 |
rs46083974 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116247671 | AAAGCACATCAGACG[A/G]TCATGAAGATGTGTC | 217935 |
rs46084570 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Wdr60 | Mm_Celera | 12:116224202 | TTAGACAAACAGTTC[A/G]CCTTTCTCAGCATCA | 217935 |
rs46090157 | snp | C/G | 0.459184 | 0.136902 | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116234701 | ATCAGCTTTCTGAAA[C/G]GTATGAATTCACACA | 217935 |
rs46110404 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116260083 | ACCTCAAGGTAAGCC[C/T]CCCCCCCCCCAGTGG | 217935 |
rs46122242 | snp | A/G | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235485 | TGTGATGATGTCTGG[A/G]GCACTGACACCTTTG | 217935 |
rs46127601 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116213074 | AAGGAATGGTGATTG[C/T]TTTGTGGACTGGGTT | 217935 |
rs46136164 | snp | C/G | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116214002 | CGCTCCTATCAGGCT[C/G]CCTCCAATGAGGAGC | 217935 |
rs46147504 | snp | A/G | 0.18 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116207202 | AAACAGAAGGCTGAT[A/G]GAGGCCACCTCCAAA | 217935 |
rs46153720 | snp | A/G | 0.18 | 0.24 | intron-variant | Wdr60 | Mm_Celera | 12:116214050 | CGCCAATAAGGAGCC[A/G]CTCCTATCAGGCTGC | 217935 |
rs46210515 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116218683 | GCCTGCCATTTCTAA[C/T]GAAAGCAGAAACAAA | 217935 |
rs46253723 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Wdr60 | Mm_Celera | 12:116241490 | GTTCAATCCCTAAAC[A/C]ATCAACAATGAAAAT | 217935 |
rs46260079 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116240931 | AGGGTTCTCCACTAC[A/T]TAGGGCTGCCCGCAT | 217935 |
rs46301578 | snp | A/T | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116246937 | GGATTATTTTAAGAG[A/T]TGCCCTTGTAAGAAC | 217935 |
rs46301788 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116222866 | CACAACCATCCATAA[C/T]GAGATCTGATGCCCT | 217935 |
rs46324493 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116232388 | AGGGATCAGACTAGG[A/G]TTCAGGCCAATTTAA | 217935 |
rs46325536 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116252151 | GTGTATACAGTGACA[C/T]GTGCTGCCTGTGTGT | 217935 |
rs46331790 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116223928 | GATTCTCATCTTCCC[A/G]AATCTGGACAGAGCA | 217935 |
rs46339732 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116259938 | ACGTATACATACATT[C/T]GTGCACACACACAAC | 217935 |
rs46341160 | snp | G/T | 0.42 | 0.183303 | missense, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116218785 | GGATCTCGTACCTTC[G/T]TGAGTAGAAAAGGGT | 217935 |
rs46349366 | snp | A/T | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116236520 | CAGAGTCTCATTTAA[A/T]GTTTGTTAGCTCTGC | 217935 |
rs46352404 | snp | A/T | 0.441482 | 0.160732 | intron-variant | Wdr60 | GRCm38.p3 | 12:116248864 | TGTGCTGCTTGTGTA[A/T]TACAGTGACACGTGC | 217935 |
rs46354763 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116206344 | AGGGGGTAGTTACAC[A/G]AGAACTAAAAGAGAA | 217935 |
rs46357192 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116232115 | TATAGAAAATTCCTT[A/T]TAAAAAAATTTTTTT | 217935 |
rs46367882 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116245324 | CTGAGGCCATAGTAC[C/T]AGTACCTGGGTACCA | 217935 |
rs46380306 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116252096 | TGCATTATAGTGACA[C/T]GTGCTGCTTGTGTGT | 217935 |
rs46390998 | snp | G/T | | | downstream-variant-500B | Wdr60 | Mm_Celera | 12:116205786 | AGTGCCTCATCCAAC[G/T]CCCACATCTGTAACT | 217935 |
rs46391012 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Wdr60 | GRCm38.p3 | 12:116251753 | AATGACATGTGCTGC[C/T]TGTGTAATACAGTGA | 217935 |
rs46394112 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116259988 | ACGAAAACAATTCAA[A/G]ACATGAAGAAATTGA | 217935 |
rs46401155 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116210135 | ACACACACAGCCTTT[C/T]GGGCACAACAGGCCT | 217935 |
rs46435707 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116232216 | GCTAAACTGCACTGA[A/T]GGAACACATCTTGAA | 217935 |
rs46460694 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116213067 | TCTCAGGAAGGAATG[A/G]TGATTGTTTTGTGGA | 217935 |
rs46474749 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116232910 | CTGCCTAAAAGCAGC[C/T]GACACAATCCCTGGG | 217935 |
rs46500771 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116214044 | GGCTGCCGCCAATAA[A/G]GAGCCACTCCTATCA | 217935 |
rs46506512 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116206911 | CCTAGCCCTCGACTC[A/C]TAGCCCTAGAGTCCC | 217935 |
rs46519231 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116231022 | GCACAGACTTCCTCA[C/T]GCTGTTGTATCCCTC | 217935 |
rs46531913 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116209896 | TATACCGATAGATCA[A/G]TGTCTTGCTCAGCCA | 217935 |
rs46561845 | snp | A/G | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116213982 | GGCTGCCTCCAATGA[A/G]GAGCCGCTCCTATCA | 217935 |
rs46562153 | snp | A/C/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116260999 | GCTAGAAAAGGTATT[A/C/T]CAAGCAAATCGGCCC | 217935 |
rs46581257 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116241198 | GAGATCAGTACCACA[A/G]AGCGACAGTGCTAGC | 217935 |
rs46582525 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116260617 | CCAGCAAAACTATCA[A/G]TCACAATCCATTCAG | 217935 |
rs46619694 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Wdr60 | GRCm38.p3 | 12:116248720 | TGACATGTGCTGCCA[G/T]TGTGTATTACAGTGA | 217935 |
rs46626745 | snp | C/T | 0.459184 | 0.136902 | intron-variant, utr-variant-5-prime | Wdr60 | Mm_Celera | 12:116234512 | TCAGTGTGTCAAGGC[C/T]GATGTTCCCCACCCT | 217935 |
rs46643018 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116240342 | TTTGTTTCTTCAATA[C/T]AAACTGTTCATCATA | 217935 |
rs46654708 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116214491 | TCACATCCCAAACTT[G/T]TAGGTTCCTGAGCCC | 217935 |
rs46654808 | snp | G/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116210407 | AATGGACTGTTTTGT[G/T]TTTTTTTTTGTCTTT | 217935 |
rs46702847 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Wdr60 | Mm_Celera | 12:116245513 | ACACAGCGTGACTGC[C/T]GATTACTCTTCCAGA | 217935 |
rs46703243 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116238033 | GGTTCGGCTTGATCT[A/G]TGATGCTTGCAAACC | 217935 |
rs46719101 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116239778 | TGTCTAGTAATTTAC[C/T]GTATATTAGACATTG | 217935 |
rs46787499 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116252498 | AAGGCTGAGGGGACT[A/C]TGGGCTTTGTTTTCC | 217935 |
rs46793613 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Wdr60 | Mm_Celera | 12:116245667 | GGTGATAGGCCTTGC[A/T]AGCTCCACAGAAGCC | 217935 |
rs46794870 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Wdr60 | Mm_Celera | 12:116208383 | TGCCAAAGCCCACAA[A/G]TCCACTCTCCAGCTG | 217935 |
rs46807770 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Wdr60 | GRCm38.p3 | 12:116206761 | CTTGGAGGCTGACAG[C/T]AGCCTAAGCAGAACC | 217935 |
rs46814596 | snp | C/G | 0.124444 | 0.216185 | downstream-variant-500B | Wdr60 | Mm_Celera | 12:116206057 | CCTTATGGAGAGAAA[C/G]CAGCCAACTACAGCA | 217935 |
rs46816684 | snp | A/C | | | downstream-variant-500B | Wdr60 | Mm_Celera | 12:116206006 | CTGCTCCTTGTGACT[A/C]AGTGGCCAGTATGAC | 217935 |
rs46826839 | snp | C/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116214004 | CTCCTATCAGGCTGC[C/T]TCCAATGAGGAGCCG | 217935 |
rs46854807 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116247944 | CTGAGCAACACAAGC[A/G]CTACCTGTTGACTTC | 217935 |
rs46871145 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116208257 | ATACCTCCAACAATG[A/G]GACCTTCAAACTGCT | 217935 |
rs46879710 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116233257 | TCTAATATTGCAGAG[C/T]AGACACAAGGCACAT | 217935 |
rs46884442 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116245755 | GCACTCACAGCATGT[C/T]GGGAAGCATACTGGC | 217935 |
rs46886762 | snp | C/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116249628 | AGTGACATGTGCTGC[C/T]TGTGTGCATTACAGT | 217935 |
rs46893658 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116232925 | TGACACAATCCCTGG[G/T]CTTGGGTCCTGAACT | 217935 |
rs46905831 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116242137 | TGAGTAGCTTGAAAA[C/T]CTCACAACGTTTTGT | 217935 |
rs46909407 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116207953 | ATCCCAGCACTTGGG[A/T]GGCAGGGGCAGGCAG | 217935 |
rs46917834 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116230349 | ATTAGCAGAAATGGG[C/G]AAAGGAAGCAAAAGA | 217935 |
rs46930066 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116213413 | TGAAAAGTCAATCAC[A/G]TTAACTTTTATGGGT | 217935 |
rs46937071 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Wdr60 | Mm_Celera | 12:116219080 | CCGTGATTTTCAGCA[C/T]CTCTAGCAAACAGAG | 217935 |
rs46947918 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116240313 | CTTTTGGTTTTTTGG[G/T]TTTTTTTTGTTTGTT | 217935 |
rs46953872 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264061 | TTAATGAGCAGAGCA[C/T]ACCTGTAACAAAGGG | 217935 |
rs46959566 | snp | C/G | 0.18 | 0.24 | intron-variant | Wdr60 | Mm_Celera | 12:116219889 | CTTCACAGTTTCACA[C/G]TCCTGCGTTCTGCTC | 217935 |
rs46962572 | snp | A/G | 0.426035 | 0.177515 | downstream-variant-500B | Wdr60 | Mm_Celera | 12:116206041 | AACAAAGACAGTGCC[A/G]CCTTATGGAGAGAAA | 217935 |
rs46969632 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116212599 | AGATTAATTCTTCCT[C/T]GCTCTTTAATCCCTT | 217935 |
rs46986231 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116206475 | TCTCGCTGGGAAAGG[A/G]CAGAAAGAGCTTTAA | 217935 |
rs47001520 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr60 | Mm_Celera | 12:116246324 | TCAGCAAAACTCTTA[C/T]AGCTAATTATAATTC | 217935 |
rs47010022 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116246027 | GGGCTCCTTTGTATA[C/T]TCCGTCCAACCTTGC | 217935 |
rs47023980 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116259794 | GAAGCCAGCAACCCT[C/T]TGTCACAGACAAGGA | 217935 |
rs47033603 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Wdr60 | GRCm38.p3 | 12:116250277 | AGCTGCCTCTGTGTA[A/T]TACAGTGACATGTAC | 217935 |
rs47057654 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116239779 | GTCTAGTAATTTACT[A/G]TATATTAGACATTGT | 217935 |
rs47063985 | snp | A/C | 0.46281 | 0.131194 | intron-variant | Wdr60 | Mm_Celera | 12:116213616 | GCAAACAGTAAATTA[A/C]TCTGATATAAAGTTA | 217935 |
rs47069012 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116262218 | AAAAGAGTAGATGGC[A/C]CAAAAAAAAAAAAAT | 217935 |
rs47118338 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116260964 | ATGAATGACAGACAT[C/T]ACCTTAGGGATTTAA | 217935 |
rs47119259 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Wdr60 | Mm_Celera | 12:116246612 | CAAATCTTACCAGAC[A/G]CGAACAAGAGAGAAA | 217935 |
rs47123111 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116253621 | GAAAGGACCCAAGGA[A/G]CTAAAGGGGTCTGCA | 217935 |
rs47154832 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Wdr60 | Mm_Celera | 12:116245812 | CTTTATGAAATTAAA[A/G]TTCTTACTTGGTGAA | 217935 |
rs47172868 | snp | A/C | 0.486111 | 0.0821678 | intron-variant | Wdr60 | GRCm38.p3 | 12:116213179 | TTTCTAAAGAGAGTT[A/C]AATTTCTGAGTCAAT | 217935 |
rs47186194 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116232116 | ATAGAAAATTCCTTT[A/T]AAAAAAATTTTTTTT | 217935 |
rs47246824 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116218920 | AAGATCCACAGCACC[C/T]ACTGTAAGTCTCACA | 217935 |
rs47253638 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116230965 | ACCTTTATGCTTGTC[C/T]TTATGACTAAGACTG | 217935 |
rs47273862 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116246247 | TAGGAAGGTGTGGGG[C/T]GGCTTAAGGCAAGTG | 217935 |
rs47290670 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Wdr60 | Mm_Celera | 12:116207840 | AGTGTGTGACTTTCC[A/G]TTACCAGAGTAAATA | 217935 |
rs47313322 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr60 | Mm_Celera | 12:116252728 | TACACACAGCAAAAC[A/G]AACAGCATTTGACTT | 217935 |
rs47316299 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr60 | Mm_Celera | 12:116245514 | CACAGCGTGACTGCC[A/G]ATTACTCTTCCAGAC | 217935 |
rs47360624 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116241530 | TAGTTTTAAGATTAT[A/G]TTGATGAAGAGTACA | 217935 |
rs47376150 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116253642 | GGGGTCTGCAACCCT[A/C]TAGGAGGAACAACAA | 217935 |
rs47397151 | snp | A/G | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264522 | GTCCCTAATTAGATT[A/G]TACACTAATTTATAA | 217935 |
rs47397951 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116246876 | ATGTGTTTTCTAGGA[G/T]TCATGTGATGCTGAT | 217935 |
rs47403346 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116223732 | TTAGTTCTTCTGAGT[A/G]CAAGTTGAAACCACA | 217935 |
rs47405470 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116233139 | CAATTATTTATCATG[C/T]CCCAAGAGGCTATGT | 217935 |
rs47421425 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116262386 | GAAGACCTAAATTAA[C/T]TAAAGCAGACAAGGG | 217935 |
rs47470503 | snp | G/T | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Wdr60 | GRCm38.p3 | 12:116234909 | ACATCTTTGCTAAAT[G/T]CATTCATTATTCACA | 217935 |
rs47516933 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116208488 | CTGTGTGCCCTCTGC[A/C]TGCCATTGCCCTACC | 217935 |
rs47528275 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Wdr60 | Mm_Celera | 12:116240613 | CCTTTGCGTGTGAAT[A/G]CATGCTTCTGACTTA | 217935 |
rs47544556 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116228104 | ACTGTGCACTGTGAG[C/G]CTATCTGCCTCCTAT | 217935 |
rs47562705 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116237275 | ATAATGTTTAATTTC[C/G]CAACTTCTGGCAATT | 217935 |
rs47571246 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Wdr60 | Mm_Celera | 12:116252083 | TGTGCTGCCTGTGTG[C/T]ATTATAGTGACATGT | 217935 |
rs47583182 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr60 | GRCm38.p3 | 12:116249965 | ACACGTGCTGCCTGT[A/G]TTACAGTGACATGTG | 217935 |
rs47605134 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Wdr60 | GRCm38.p3 | 12:116249942 | TGTGCTGCTTGTGTA[A/T]TACAGTGACACGTGC | 217935 |
rs47615200 | snp | A/T | 0.48 | 0.0979796 | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116233395 | ATCCAGGAGAGAAAA[A/T]GTGAACGAAAAGTCT | 217935 |
rs47626963 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116206389 | TCTTTGGGAAATAAG[A/G]ATATGTCCCCATGGA | 217935 |
rs47630879 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116260391 | CAAACCAGAAAGAAA[C/T]TCCCTACAACACATA | 217935 |
rs47635274 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116260361 | CTATCAAGTTATAAC[A/G]GGTATGCAGAATACC | 217935 |
rs47655199 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116259684 | AGCTAGAGCAGATAT[C/T]TACACCAAGAAACAC | 217935 |
rs47665992 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116241785 | AATCATTTGCATCTG[C/T]ATAAGAAAAATAAAA | 217935 |
rs47673691 | snp | A/C | 0.444444 | 0.157135 | downstream-variant-500B | Wdr60 | Mm_Celera | 12:116206035 | ACAGTGAACAAAGAC[A/C]GTGCCGCCTTATGGA | 217935 |
rs47678517 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116231115 | TAACTAGAAACTTAG[C/T]GGAAATGTTCACCAT | 217935 |
rs47684216 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Wdr60 | Mm_Celera | 12:116227545 | TACTGACAAAAGTTT[A/G]TAACTGCTGTATTCT | 217935 |
rs47744682 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116247062 | CAATATACATGTGAC[C/T]GATACAGGACAACTG | 217935 |
rs47753274 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116247558 | ACTCTCCCTCTATTA[A/G]TTACAAAATATTGAT | 217935 |
rs47755991 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr60 | Mm_Celera | 12:116211466 | TGTAAAATGGAATAG[A/G]ATGTGCATGACATGT | 217935 |
rs47766404 | snp | A/G | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116238127 | TCACTACGACATAAC[A/G]TGACATAGCCTTCTC | 217935 |
rs47798148 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116222828 | CGGTCCAGAGTTCAA[A/T]TCCCAGCAACCACAT | 217935 |
rs47806853 | snp | A/G/T | 0.5 | 0 | intron-variant | Wdr60 | GRCm38.p3 | 12:116240712 | CCGAGTCATTTCTCA[A/G/T]GGGAAAGAAAGCAAG | 217935 |
rs47812289 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116244947 | CTCCTGCCCTAAGGC[A/G]CTTATATTATAGTCT | 217935 |
rs47813097 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116247085 | GACAACTGTTTCAGG[C/T]TCTATAAAAGCAGCA | 217935 |
rs47830032 | snp | C/T | 0.422832 | 0.180636 | intron-variant | Wdr60 | GRCm38.p3 | 12:116250247 | TGTGCTGCCTGTGTG[C/T]ATTATAGTGACATGT | 217935 |
rs47860571 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116259967 | ACCAGACAGTTCAAA[G/T]AAATAACGAAAACAA | 217935 |
rs47888118 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116222793 | GGCTCAGCAGTTAAG[A/C]GCACTGACTGTTCCT | 217935 |
rs47893698 | snp | A/G | 0.46875 | 0.121031 | downstream-variant-500B | Wdr60 | Mm_Celera | 12:116206084 | AGCAGTACCTGACTG[A/G]ATCAGCATCTGGATG | 217935 |
rs47894208 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116230424 | TGTGCCATGCACAGA[C/T]ACCATGGGAGCACAG | 217935 |
rs47910144 | snp | G/T | | | intron-variant, upstream-variant-2KB | Wdr60 | GRCm38.p3 | 12:116234963 | ATGTAGATTTTAAAA[G/T]TCTATCTATATAATC | 217935 |
rs47947452 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116245511 | GCACACAGCGTGACT[A/G]CCGATTACTCTTCCA | 217935 |
rs47954173 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Wdr60 | Mm_Celera | 12:116222752 | TTATGTACACTGACC[C/T]AAAAGTAAACCCTAG | 217935 |
rs47976787 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116231669 | AATTCCCAGAAGAGG[A/G]CACGCAGCACAGAAA | 217935 |
rs47982345 | snp | C/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116223639 | TTTTTTTTTTAAAAA[C/T]GGGCAAACATTTAAA | 217935 |
rs48001170 | snp | G/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116234583 | TGATAACTGGGTTCC[G/T]TAACTAACTTTGGCA | 217935 |
rs48004553 | snp | A/C/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116208053 | CCTGTCTCAAAAAAA[A/C/T]CAAAAAAAAAAAAAA | 217935 |
rs48005133 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr60 | Mm_Celera | 12:116243801 | ACATTTAATTATGTA[C/T]TAATCTGCCTCCTCA | 217935 |
rs48010188 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116260131 | AATTCCAGGTCTGTA[C/T]ACAAGGTAGAAGAAA | 217935 |
rs48023538 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Wdr60 | Mm_Celera | 12:116236745 | TCTCCAAGGCTCCTG[C/G]CGCCTACTTGGACCT | 217935 |
rs48028867 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116222862 | GGCTCACAACCATCC[A/G]TAACGAGATCTGATG | 217935 |
rs48031974 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116238122 | TCTTATCACTACGAC[A/G]TAACATGACATAGCC | 217935 |
rs48059419 | snp | C/T | 0.124444 | 0.216185 | missense, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116248005 | AATACCTTCAATTCC[C/T]TTTTCTTGTGCTCTT | 217935 |
rs48059631 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr60 | Mm_Celera | 12:116236949 | GCAGCACCCAAGATG[A/G]AAAATTTAAATTCTC | 217935 |
rs48068698 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116252292 | GATCCAGAAGAAGAA[G/T]AATCCTCATTCACAC | 217935 |
rs48084102 | snp | C/T | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116263739 | AAGCAGGCTGCCCCA[C/T]CTGACTTTTACGTGG | 217935 |
rs48088309 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116244998 | AGAAAGGTCACACTG[C/T]TAGCCAATGCTAAAA | 217935 |
rs48095714 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116230408 | GTAGGTTGGACAGAG[A/G]TGTGCCATGCACAGA | 217935 |
rs48101599 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116241030 | AGGAGTTCAAGGGAG[C/T]CTAATTAATGTCTGA | 217935 |
rs48111119 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116208402 | ACTCTCCAGCTGAGG[C/T]CTGCCCTGAGCTCCA | 217935 |
rs48127652 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116225699 | AAATATCCTGGCCTT[A/G]TGGCCATCCTGACCA | 217935 |
rs48133054 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116226689 | GCAGAGCTGCTTTCC[A/G]TACGGTTCTCATTAG | 217935 |
rs48134141 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116247546 | ACTACAATTACTACT[C/G]TCCCTCTATTAGTTA | 217935 |
rs48148273 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116252770 | CACCACATTCTTAAT[C/T]TGTCCCCTCAATTTA | 217935 |
rs48155288 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116240698 | AATCACTGGTCATTC[C/T]GAGTCATTTCTCAAG | 217935 |
rs48192131 | snp | C/G | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116234747 | TATAATAGAAAGGCA[C/G]TTTTTTTGTTTCCTA | 217935 |
rs48196161 | snp | C/T | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116263299 | ACCTTTAGTTAATTC[C/T]ATTACAATGGAGACA | 217935 |
rs48211988 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116240126 | ACCCAAAGAGTCCCT[A/G]GAATAGGAAAATAGA | 217935 |
rs48228072 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116211554 | TTGCACAACTGGGGG[G/T]AGGGGGTCCAAGTAC | 217935 |
rs48229631 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116232190 | CTGCAGATGCCTGTA[A/T]CTTAGAGACTGCTAA | 217935 |
rs48230913 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | Wdr60 | GRCm38.p3 | 12:116235778 | TTAATCCCAGCACTC[A/G/T]GGAGACAGAGGCAGG | 217935 |
rs48230970 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Wdr60 | Mm_Celera | 12:116231916 | CTTCACACTGCTTTA[A/C]AGGAAGTTCAGAGAC | 217935 |
rs48253122 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Wdr60 | GRCm38.p3 | 12:116248781 | TGTGCTGCCTGTGTG[C/T]ATTATAGTGACATGA | 217935 |
rs48268353 | snp | C/T | 0.297521 | 0.245442 | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116226046 | GTGCCTGCTATCCAG[C/T]GATGGGGCAAAAGCC | 217935 |
rs48281217 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116210980 | GGTTCAGCCAGTAAC[A/G]GCACTTGCTATCAAA | 217935 |
rs48314083 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116247847 | ATAAGTCCTTCCTCC[C/G]TTGACTTAAGGCTGA | 217935 |
rs48325815 | snp | G/T | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Wdr60 | Mm_Celera | 12:116234407 | GACAGGGCTCAGCTT[G/T]CGGTTTCCACACCTT | 217935 |
rs48334156 | snp | A/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116223633 | TAAATCTTTTTTTTT[A/T]AAAAACGGGCAAACA | 217935 |
rs48338064 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116212619 | TTTAATCCCTTCCAT[A/G]CTCAAAAAAGATACA | 217935 |
rs48339108 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116245355 | TGGTACAGTACCACA[C/T]AGTACAATCCACACA | 217935 |
rs48358733 | snp | A/G | 0.493827 | 0.0552116 | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264816 | CACCTTTGATAGTTG[A/G]AACTACTTAGGCTAG | 217935 |
rs48359289 | snp | A/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116213169 | AAACAAAGTATTTCT[A/T]AAGAGAGTTCAATTT | 217935 |
rs48377156 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116232704 | ATTGTACTGAACATA[C/T]GCCTTAGAGGCAAAA | 217935 |
rs48406128 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116257644 | AATTTTGCATTCTCA[A/T]TATACTATTTATATC | 217935 |
rs48447142 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116241826 | GACAATTAAATAATT[C/T]CTTCAAGGAAAAAAA | 217935 |
rs48456002 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | Wdr60 | GRCm38.p3 | 12:116235755 | GCTGGGCGTGGTGGC[A/C/G]CATGCCTTTAATCCC | 217935 |
rs48458149 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116223384 | CTTAAGACAGCCAGA[C/G]TCCATAATTAGACCT | 217935 |
rs48512755 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116210928 | AAGAATAAAGGCAAA[A/G]AATTATTTCAAAGTA | 217935 |
rs48531126 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116229859 | CCTCTGGCCTCTGCA[A/G]GACCAGAATGCACAC | 217935 |
rs48537415 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116247646 | ACGGAGAAGCATTGA[C/G]AATATTTATAAAGCA | 217935 |
rs48542695 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116207535 | CATATTCTATGTACA[C/G]AGAATCACATGAACA | 217935 |
rs48553043 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116212402 | AGCAGCCGTCAGTGC[A/G]CCCAATGGAAACTGT | 217935 |
rs48577345 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116208181 | CTCCAGATGACAACT[C/T]CCACCACTTCACACA | 217935 |
rs48582375 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116208296 | CTCCCAGCCACACAG[A/G]CAGTGGGAGGATCCC | 217935 |
rs48603979 | snp | C/T | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116240738 | GCAAGACAAAAAGCC[C/T]TCTTCTTCCTTGCCT | 217935 |
rs48636339 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116232854 | GTTGGGATAAGGTTA[A/G]CCTGTGGGGGACTTT | 217935 |
rs48670323 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Wdr60 | Mm_Celera | 12:116241639 | GTTTCATCCACAAAC[A/G]CACACATACAACCCT | 217935 |
rs48704898 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Wdr60 | Mm_Celera | 12:116218288 | TGCTTCATAAAAAAA[C/G]ACTAATCATCTGCTT | 217935 |
rs48710300 | snp | C/T | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116247129 | GTATGAGAACAAAAG[C/T]CACCACAGTGGTCTC | 217935 |
rs48716749 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116246087 | AACCCTTTCATTCTC[C/T]GCACTGATCGCCTTT | 217935 |
rs48722740 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116252219 | GCATGATGCTATCGA[G/T]GTATATTACAGTGAA | 217935 |
rs48723093 | snp | C/G | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Wdr60 | Mm_Celera | 12:116234338 | TTTCCTGCCACAGAA[C/G]AACATTCCACACTTC | 217935 |
rs48763762 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116245485 | CCCAATAGCTGGCTA[A/C]TTCTGCAGCAGCACA | 217935 |
rs48774562 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Wdr60 | Mm_Celera | 12:116241668 | CTGTGACAAATTCTT[C/T]ATATACCTACTTTTG | 217935 |
rs48781591 | snp | A/C/G | 0.165289 | 0.235211 | intron-variant | Wdr60 | GRCm38.p3 | 12:116208486 | CCCTGTGTGCCCTCT[A/C/G]CATGCCATTGCCCTA | 217935 |
rs48802115 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116228720 | CTCTGTCTCCTGAAG[C/G]AAGCATCACTGCTGG | 217935 |
rs48814180 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116260497 | AAGGCAGGCCCACTA[A/G]AGTAACATCTTGACT | 217935 |
rs48814841 | snp | A/G | | | downstream-variant-500B | Wdr60 | Mm_Celera | 12:116206085 | GCAGTACCTGACTGA[A/G]TCAGCATCTGGATGT | 217935 |
rs48818826 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Wdr60 | GRCm38.p3 | 12:116250989 | TGTGCTGCCTGTGTG[C/T]ATTATAGTGACATGA | 217935 |
rs48823298 | snp | G/T | 0.444444 | 0.157135 | downstream-variant-500B | Wdr60 | Mm_Celera | 12:116206230 | TGAATGAGCTCTGAG[G/T]CAACACGATGAAAAA | 217935 |
rs48823820 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116237016 | CCAGTTCTTGCAGAG[A/G]ACCCAAGGTCAATTC | 217935 |
rs48838472 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116228774 | TTCACAGCCAGAACC[A/G]TGACAGCTCAGCTAC | 217935 |
rs48864451 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116259928 | CTGTGAACACACGTA[C/T]ACATACATTCGTGCA | 217935 |
rs48871405 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Wdr60 | Mm_Celera | 12:116208156 | AGGCAGCAGCTCACA[A/G]ACTGTGTAGCTCCAG | 217935 |
rs48873367 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116214980 | CATGGCAAGACCAGC[C/T]CCAACTCCCATTTTT | 217935 |
rs48880546 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116213556 | TTAGACACAAGACTG[A/G]ACAACACAATATTCA | 217935 |
rs48892161 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116260636 | CAATCCATTCAGAAA[A/G]AAAAACATGATACAA | 217935 |
rs48903935 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116246859 | GCAGAGAAGTTGGAA[A/G]TATGTGTTTTCTAGG | 217935 |
rs48928734 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116213259 | ATCACTGAGGTCCAA[C/G]TAATGATTAGTTTGT | 217935 |
rs48931304 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116226271 | CCTGAACCATTCTGA[A/G]ACAAGTTATTCAGTA | 217935 |
rs48950586 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116206717 | CTGTCCTTCACCTTT[A/G]CCAAGTAAGGACATG | 217935 |
rs48953860 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Wdr60 | GRCm38.p3 | 12:116249175 | AGCTGCCTCTGTGTA[A/T]TACAGTGACATGTAC | 217935 |
rs48975285 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Wdr60 | Mm_Celera | 12:116211647 | TGACTATATAGTACA[C/T]ACAAATGTGGTGTTA | 217935 |
rs48985673 | snp | A/G/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116262706 | AAGAAGTGAGAGGCA[A/G/T]CAGCAGAGCTGAGAC | 217935 |
rs49002239 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116238190 | GGTAAAGGTATGTTT[A/G]CTTGACACAGCTTCC | 217935 |
rs49035163 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Wdr60 | Mm_Celera | 12:116223847 | ACAGTGTGCAATAGA[A/G]CAGCAAGCCGCTGAG | 217935 |
rs49039345 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116208255 | CAATACCTCCAACAA[C/T]GGGACCTTCAAACTG | 217935 |
rs49043845 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr60 | Mm_Celera | 12:116232275 | TGAGAATAAACTGTG[C/T]TGTTCTCAGAGCAGA | 217935 |
rs49048844 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116220039 | AGAACAACTGTCCTG[A/T]GCTACGCATGAACAG | 217935 |
rs49068849 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116238663 | AAGTAGTAAAGAAGA[A/T]ATTTATTCTATCTAA | 217935 |
rs49104599 | snp | A/T | 0.124444 | 0.216185 | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264572 | CAAACAAAGCCTTTT[A/T]ATTTCACAGTGAAAA | 217935 |
rs49115400 | snp | A/G | 0.165289 | 0.235211 | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264424 | CACCACTTTCCTACA[A/G]ATTTAATTCAAAGTT | 217935 |
rs49116544 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116239865 | CAGAATCCAAATAGG[C/G]CACACTCAACAGGTC | 217935 |
rs49156493 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116257327 | TCTGAAATGAACTTG[G/T]AAGCAAAGCTATGTA | 217935 |
rs49177337 | snp | C/T | 0.5 | 0 | intron-variant | Wdr60 | GRCm38.p3 | 12:116251067 | AATGACATGTGCTGC[C/T]TGTGTAATACAGTGA | 217935 |
rs49209788 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116209697 | TAGTGGCATAAATGT[G/T]GTTGGAGTAACCACA | 217935 |
rs49232035 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Wdr60 | Mm_Celera | 12:116224247 | TGACAGTCATGGATA[C/T]AAAACACTTAGAAGA | 217935 |
rs49237825 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116252740 | AACAAACAGCATTTG[A/C]CTTCTTTGTTTCTCC | 217935 |
rs49238732 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Wdr60 | Mm_Celera | 12:116213834 | ACAAAGTGACAAGCC[A/G]CTCCTATCAGCTCCC | 217935 |
rs49250915 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Wdr60 | Mm_Celera | 12:116212057 | GTACAATAACATTTT[A/G]GCTTGCTCTTGTTTT | 217935 |
rs49281825 | snp | C/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116249635 | TGTGCTGCCTGTGTG[C/T]ATTACAGTGACATGT | 217935 |
rs49288099 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116210779 | AAAACTATTTTTAAT[A/T]TAAAAAAAAGACCCC | 217935 |
rs49297504 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116226287 | ACAAGTTATTCAGTA[C/G]TAAGGACTTTATCCC | 217935 |
rs49340832 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116240772 | TCGTTACCCTGCTTG[C/T]AACATTTCTCTGTGG | 217935 |
rs49346025 | snp | A/T | 0.444444 | 0.157135 | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116206309 | TTGCTGGAGGGGTAG[A/T]TACACAAGGATGAGA | 217935 |
rs49354468 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116232817 | CTAATACACTTTTTT[A/T]AAAAAGTAAAGTATA | 217935 |
rs49402561 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116223920 | ACATGTGTGATTCTC[A/G]TCTTCCCGAATCTGG | 217935 |
rs49427733 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116232134 | AAAAATTTTTTTTTT[A/T]AAAAAAAGGTCAATG | 217935 |
rs49444425 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116252584 | TGTGCATCCCTACAA[C/T]GTGCTACCTCTCTAC | 217935 |
rs49447868 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116223019 | CTGTGACTTTTAGTT[A/G]AATAAAAACTGTTCA | 217935 |
rs49496420 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Wdr60 | Mm_Celera | 12:116226674 | AGTAAGACTTCTTTG[A/G]CAGAGCTGCTTTCCA | 217935 |
rs49520381 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116262952 | GCCGTCGCTCAGCTC[G/T]ACCAGCCAGCCAGGC | 217935 |
rs49526368 | snp | A/T | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116263081 | GCGCCTGCGCGCCCG[A/T]GTTTTCTGCAAACAC | 217935 |
rs49538420 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116237097 | TCTTCTAGCATGTAG[A/G]CATAATGCAGATAGA | 217935 |
rs49552675 | snp | C/T | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235710 | CCACCAGCTCTCACA[C/T]TGTATCTGGTGTAAG | 217935 |
rs49597474 | snp | C/T | 0.340265 | 0.233136 | intron-variant | Wdr60 | GRCm38.p3 | 12:116249221 | AATGACATGTGCTGC[C/T]TGTGTAATACAGTGA | 217935 |
rs49603287 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr60 | GRCm38.p3 | 12:116229963 | CCACCCCCAAGGTAA[A/G]CCATACTTCTTAAAA | 217935 |
rs49629242 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116262883 | CTCCTCGAGGCCGGG[A/G]CAGCCGCGTGTCCTC | 217935 |
rs49637229 | snp | A/C | 0.5 | 0 | intron-variant | Wdr60 | GRCm38.p3 | 12:116232191 | TGCAGATGCCTGTAT[A/C]TTAGAGACTGCTAAA | 217935 |
rs49650339 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Wdr60 | Mm_Celera | 12:116212715 | GAGACACATTTTAAA[C/T]GCTAATTTCATATAA | 217935 |
rs49652539 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116212823 | TCAGACACAAAAAGC[A/G]TCTTGGATACTGAAA | 217935 |
rs49687233 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264434 | CTACAGATTTAATTC[A/G]AAGTTTATAACTTAT | 217935 |
rs49702977 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116213880 | CTCCTATCAGGCTCC[C/T]TCCAATGAGGAGCCG | 217935 |
rs49718545 | snp | C/T | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235758 | GGGCGTGGTGGCGCA[C/T]GCCTTTAATCCCAGC | 217935 |
rs49756066 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116213058 | GGCTTGTGGTCTCAG[A/G]AAGGAATGGTGATTG | 217935 |
rs49764745 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116252608 | TCTCTACAACAGGGC[C/T]GACCAGTCATGGGCT | 217935 |
rs49777592 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116233563 | CTAAAGTATTCAAAA[A/T]TTATTTTAAATAATT | 217935 |
rs49780854 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116259709 | AAACACTTCAAATAT[C/T]TGAATTCCAGATGCC | 217935 |
rs49787972 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116263032 | CGGGCCGAAGGCGCT[A/G]GCCCAGCATGCCCCG | 217935 |
rs49800939 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116240186 | TCTTGTGGAGCTTGA[C/T]CCTTTGCGTCCTGGT | 217935 |
rs49803087 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116231240 | CAACAAAAGATCTTT[C/T]TCTTTTAGAAATTTA | 217935 |
rs49809654 | snp | A/G | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264833 | ACTACTTAGGCTAGT[A/G]GAAAGGCTGGACTGA | 217935 |
rs49815884 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Wdr60 | Mm_Celera | 12:116225294 | ACTATCCATGTACAC[A/G]GGTACACACCATCAA | 217935 |
rs49829534 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116226829 | GCTGACTAGTTCCTG[A/C]GGATCAGAGTTGTCC | 217935 |
rs49829834 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116245585 | ATTAACTTGATTCAT[C/T]GTGGACTACAAGATC | 217935 |
rs49842758 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116228390 | CGATGCAAGTACAAT[A/G]ATTTACGGTTTTCTT | 217935 |
rs49852518 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116206269 | AGACGGATGAGATGC[C/T]GGGGGTAGTTTTATA | 217935 |
rs49858452 | snp | A/G | | | intron-variant, utr-variant-5-prime | Wdr60 | Mm_Celera | 12:116234244 | AGAGGCCTCACAACC[A/G]CTGTCACTCTTACAT | 217935 |
rs49881903 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116239539 | TAATTTGTTATTGAA[C/T]TAACTCATCTATTCA | 217935 |
rs49902639 | snp | C/T | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264440 | ATTTAATTCAAAGTT[C/T]ATAACTTATGTACTT | 217935 |
rs49904636 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Wdr60 | Mm_Celera | 12:116228688 | TCTGGCTTTACAGGT[A/G]CCAAAGTATGTTTTC | 217935 |
rs49905116 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116210279 | CTATCTCCAGTTCAT[A/G]TCCATCCACAGGAGG | 217935 |
rs49927242 | snp | C/T | 0.42 | 0.183303 | intron-variant | Wdr60 | Mm_Celera | 12:116223876 | AGGGAGTGCATTCTG[C/T]AACTCTCAGCAGTGA | 217935 |
rs49946436 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116237068 | ACAACCATCTAGACT[A/G]GGATCTGATGCCCTC | 217935 |
rs49967318 | snp | C/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116213113 | TGAGAGCCAGTTGAC[C/T]ATGGGTTATCTTCCT | 217935 |
rs49980605 | snp | A/C | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116247126 | CATGTATGAGAACAA[A/C]AGTCACCACAGTGGT | 217935 |
rs49988676 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116246387 | TAATATACTGCTACC[A/T]TTGTTTTTCTGAAAA | 217935 |
rs50027424 | snp | C/G | | | intron-variant, upstream-variant-2KB | Wdr60 | GRCm38.p3 | 12:116234947 | TATATCTTAGTTTTA[C/G]ATGTAGATTTTAAAA | 217935 |
rs50054858 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116223719 | AATCTTGGGATCATT[A/G]GTTCTTCTGAGTACA | 217935 |
rs50063883 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116225864 | TTTTGTCTAGAGACA[A/C]GGCACTAGAAACAGG | 217935 |
rs50068146 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116213106 | GTTGCCATGAGAGCC[A/G]GTTGACCATGGGTTA | 217935 |
rs50075352 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr60 | GRCm38.p3 | 12:116247559 | CTCTCCCTCTATTAG[C/T]TACAAAATATTGATT | 217935 |
rs50075627 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Wdr60 | Mm_Celera | 12:116246915 | ATTTGTAAAACATAA[A/C]AATTTAGGATTATTT | 217935 |
rs50077507 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Wdr60 | Mm_Celera | 12:116210815 | CCTGGCACACATATC[C/T]ACCTAATATGGTTAT | 217935 |
rs50099516 | snp | A/G | | | intron-variant, upstream-variant-2KB | Wdr60 | GRCm38.p3 | 12:116234976 | AATTCTATCTATATA[A/G]TCATGTAGCTAGTAA | 217935 |
rs50113604 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116236712 | TCATTCCTTTATAAT[G/T]TCTAATTAGTTTCTG | 217935 |
rs50168521 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116245833 | ACTTGGTGAAAATTC[A/G]AGGACATTACCAAAG | 217935 |
rs50169872 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116208221 | TTCCTATCTGATGCT[C/T]CTCCCTGCCCATGGG | 217935 |
rs50177746 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116223154 | AGAGTCTGATTTTTT[A/T]AAATAAAAATGTAAA | 217935 |
rs50206373 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116245648 | AGACCTGTTCCACAG[A/G]GCAGGTGATAGGCCT | 217935 |
rs50213511 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116242342 | TGCCAAAGAGGAACC[A/C]TTAGTACCTTCTTCT | 217935 |
rs50235448 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116260145 | ATACAAGGTAGAAGA[A/C]ATGGATAGCTCAGTC | 217935 |
rs50241199 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116246279 | GTTGATGCTCATATA[C/T]AACAAAACATTACAA | 217935 |
rs50311556 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116241363 | ACACAAAAGGGTGTG[A/T]ACTAATCAGACTAAC | 217935 |
rs50314335 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Wdr60 | Mm_Celera | 12:116239638 | TTGTTAATTTGCTTA[A/T]ACACACATTAATCAC | 217935 |
rs50320624 | snp | A/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116249018 | TGTAATACAGTGACA[A/T]GTGCTGCCTGTGTGC | 217935 |
rs50338452 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116255789 | AAACTAACAAGCAGC[C/T]TGGGTTACACTATAG | 217935 |
rs50338828 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116212612 | CTCGCTCTTTAATCC[C/T]TTCCATACTCAAAAA | 217935 |
rs50349003 | snp | A/T | | | utr-variant-5-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116262947 | AACCCGCCGTCGCTC[A/T]GCTCTACCAGCCAGC | 217935 |
rs50349578 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116248052 | TTTTTTATCTGCATG[A/G]CTTCGGCGCCTCTCG | 217935 |
rs50352788 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116261076 | TCAAGCCAAAACTAA[C/T]CAGAAGAGATAGAAA | 217935 |
rs50355316 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116234015 | TTTCACCCTAAAGGC[A/G]ATGGCACTGGATTCA | 217935 |
rs50389344 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116242340 | TGTGCCAAAGAGGAA[C/T]CCTTAGTACCTTCTT | 217935 |
rs50391770 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116240187 | CTTGTGGAGCTTGAC[C/G]CTTTGCGTCCTGGTG | 217935 |
rs50397823 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116226264 | TATCAGACCTGAACC[A/G]TTCTGAAACAAGTTA | 217935 |
rs50418970 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116212355 | AAACAGTGAGGTGAG[C/T]GACCATGAGCAATCA | 217935 |
rs50437002 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Wdr60 | Mm_Celera | 12:116232785 | TTAAAATAAAAGTAA[C/T]GACATTTTTAAAAGA | 217935 |
rs50443361 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116238210 | ACACAGCTTCCCCCA[C/T]CCATGTATTTTCAAC | 217935 |
rs50448962 | snp | A/G | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Wdr60 | Mm_Celera | 12:116234174 | TCCCAGAATCACAGT[A/G]TTAACAAGTCACTTG | 217935 |
rs50471264 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116260789 | AATCCCATTAGAGTA[A/G]ATCATCCCACAGAAA | 217935 |
rs50474238 | snp | C/T | | | downstream-variant-500B | Wdr60 | Mm_Celera | 12:116205782 | GCCCAGTGCCTCATC[C/T]AACTCCCACATCTGT | 217935 |
rs50504700 | snp | C/T | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264832 | AACTACTTAGGCTAG[C/T]GGAAAGGCTGGACTG | 217935 |
rs50511605 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116214650 | GGTCTACAACTGGGG[C/T]AAGCTCAATGCATCT | 217935 |
rs50523462 | snp | C/T | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116226613 | ATGGCCCTCAGAACT[C/T]CATGCAGAAAACTAA | 217935 |
rs50607622 | snp | A/G | 0.48 | 0.0979796 | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116207735 | CACCAGGGCCACAAA[A/G]CTACCACTGGTCTTC | 217935 |
rs50627030 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116261152 | AAAAAATAATATTGC[A/G]TTAGCATTTCTTCTA | 217935 |
rs50654615 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116228797 | TCAGCTACCTCACTG[C/G]TCACATTCTTTAAAG | 217935 |
rs50662287 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116210996 | GCACTTGCTATCAAA[A/C]CTGATGACACAAGTT | 217935 |
rs50663223 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Wdr60 | Mm_Celera | 12:116246594 | TAACTACCAGATCTA[C/T]ATCAAATCTTACCAG | 217935 |
rs50672090 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Wdr60 | Mm_Celera | 12:116228678 | ACAGCAACTCTCTGG[A/C]TTTACAGGTACCAAA | 217935 |
rs50677512 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116232323 | GGGGTGAAGTTATAT[C/T]GTGAGTATTTGGAGG | 217935 |
rs50706911 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Wdr60 | Mm_Celera | 12:116245370 | TAGTACAATCCACAC[A/G]GTAAAAAGACTGGGT | 217935 |
rs50707907 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr60 | Mm_Celera | 12:116231332 | TGAATAACAAGTCAG[A/G]TGAGGGAGGTCTGCT | 217935 |
rs50725126 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116252409 | GTCTGGATGGTCCTG[A/G]GTTAAGGCTTGGTCT | 217935 |
rs50740124 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116260826 | AACAGGAATTATAAA[C/T]ACTGCTCATTAAGAA | 217935 |
rs50761927 | snp | A/T | 0.489796 | 0.070696 | downstream-variant-500B | Wdr60 | Mm_Celera | 12:116206017 | GACTCAGTGGCCAGT[A/T]TGACAGTGAACAAAG | 217935 |
rs50788557 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116212026 | GAAGTTTTCAGAGCA[C/T]TAGCTTTCCTTGTTT | 217935 |
rs50791268 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116246615 | ATCTTACCAGACACG[A/G]ACAAGAGAGAAAATA | 217935 |
rs50802864 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116231214 | CTTTGAGACACTGTG[C/T]CTTTTTACATCAACA | 217935 |
rs50820827 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116230322 | ATCTCTAGAACGTGA[A/G]AAGACTTAAGAATTA | 217935 |
rs50846939 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116208459 | GAGCAGCCCATCCCA[C/T]CATGTGCTGACCCCT | 217935 |
rs50873363 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116246409 | TTCTGAAAATGAACC[A/G]CAGGATATAGAACCA | 217935 |
rs50876000 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116207858 | ACCAGAGTAAATATC[C/T]ATATTCAAGAGACAT | 217935 |
rs50880779 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116213327 | TGAATTACAATGTTA[C/T]ATTGCCCCAAAAGGT | 217935 |
rs50886763 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr60 | Mm_Celera | 12:116208197 | CCACCACTTCACACA[A/G]GTGTGACATTCCTAT | 217935 |
rs50890548 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116260316 | TAAAATCACGGAAGT[A/G]ACATTTCCCAACCTA | 217935 |
rs50904262 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Wdr60 | Mm_Celera | 12:116239714 | TCTCAGGATCATACA[G/T]GAATGTGCTACACTC | 217935 |
rs50922600 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116208414 | AGGTCTGCCCTGAGC[C/T]CCAGGCCCTCCACAG | 217935 |
rs50934598 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116223357 | AGGCTGAGGTCAGAG[C/T]ACTGCTATAAGCTTA | 217935 |
rs50989826 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116230980 | TTTATGACTAAGACT[A/G]TCATCAGACAGTGTC | 217935 |
rs50990005 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116246583 | CTTTGCACAGGTAAC[A/T]ACCAGATCTATATCA | 217935 |
rs51001544 | snp | C/T | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116224165 | CTCTGAGTACAGGGC[C/T]TACCCGTGCAGTCAG | 217935 |
rs51017407 | snp | A/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116223632 | GTAAATCTTTTTTTT[A/T]TAAAAACGGGCAAAC | 217935 |
rs51030480 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116246911 | AATTATTTGTAAAAC[A/G]TAAAAATTTAGGATT | 217935 |
rs51049187 | snp | A/T | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116229699 | GTCCTCTTCAAGCAA[A/T]ACAGCAACCACCTTT | 217935 |
rs51080036 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116231045 | TATCCCTCCTACCCA[C/T]TGTTCTTACAACATA | 217935 |
rs51106266 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116232816 | CCTAATACACTTTTT[A/T]TAAAAAGTAAAGTAT | 217935 |
rs51113087 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116245565 | TGCACTAGTAAGTAA[C/T]TGCTATTAACTTGAT | 217935 |
rs51145549 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr60 | Mm_Celera | 12:116238020 | TATTTTTGCTTTGGG[C/T]TCGGCTTGATCTGTG | 217935 |
rs51157222 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr60 | Mm_Celera | 12:116230284 | AGTCAGCATTAAATG[C/T]CTGCAGTGGCTCCAA | 217935 |
rs51163255 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116238667 | AGTAAAGAAGATATT[A/T]ATTCTATCTAATGTC | 217935 |
rs51223734 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116213567 | ACTGGACAACACAAT[A/C]TTCAAGAAATACGTT | 217935 |
rs51244104 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116223057 | ATCAAAAGCATGATC[A/G]TAAGAGAAAATATTG | 217935 |
rs51254112 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Wdr60 | Mm_Celera | 12:116217812 | GAAACCTAAAGTATA[C/T]TGGAAAAGAAAGAAG | 217935 |
rs51290423 | snp | A/G | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116263268 | AAATCATTTGTGGCC[A/G]ACTGCGGCAGCGCAC | 217935 |
rs51293733 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Wdr60 | GRCm38.p3 | 12:116251616 | TGACATGTGCTGCCA[G/T]TGTGTATTACAGTGA | 217935 |
rs51299780 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116262448 | GGATTTATCATGAGT[A/T]GTTAATAGGGCCATA | 217935 |
rs51301290 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116212373 | CCATGAGCAATCACC[A/G]CCGTGGACCAGACAG | 217935 |
rs51372637 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Wdr60 | Mm_Celera | 12:116211579 | AAGTACATATAGGAC[C/T]TCTGTGTATGTTTGA | 217935 |
rs51376392 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Wdr60 | Mm_Celera | 12:116218532 | TGTCTCTGACCCATT[C/G]CCCAGGGCAGGTGCA | 217935 |
rs51416153 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116247028 | TTTGAGAGGTGTTTA[C/T]TCTATAACAAACATT | 217935 |
rs51416436 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116261108 | GGACATTATATACTC[A/C]TCAAGGGGGAAAAAA | 217935 |
rs51419643 | snp | A/G | 0.48 | 0.0979796 | intron-variant, utr-variant-5-prime | Wdr60 | Mm_Celera | 12:116234471 | CATCCTTTCCCTACC[A/G]CACAACAACTACAAC | 217935 |
rs51471658 | snp | A/G | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116249207 | GCCTGTGTGTTTACA[A/G]TGACATGTGCTGCTT | 217935 |
rs51483164 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116231046 | ATCCCTCCTACCCAT[G/T]GTTCTTACAACATAT | 217935 |
rs51495991 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116260035 | CAAACTGAAATAAAT[C/T]TGGAATCCAAAGACT | 217935 |
rs51499926 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116245561 | ACACTGCACTAGTAA[C/G]TAACTGCTATTAACT | 217935 |
rs51515158 | snp | C/T | | | downstream-variant-500B | Wdr60 | Mm_Celera | 12:116205998 | GCTGCCCACTGCTCC[C/T]TGTGACTCAGTGGCC | 217935 |
rs51521778 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Wdr60 | Mm_Celera | 12:116238037 | CGGCTTGATCTGTGA[C/T]GCTTGCAAACCATGT | 217935 |
rs51531530 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116241286 | AGACCGAGGGCTCCA[C/T]GGCTTAGTCCAAAAT | 217935 |
rs51581714 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116223234 | TCTCAGTGTGTAATG[C/T]GCAGGCCTGGCAAAT | 217935 |
rs51595848 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116226379 | CCAGTCTTCCTCCAC[A/G]CCTACAGCCTAAACC | 217935 |
rs51614748 | snp | A/T | 0.32 | 0.24 | intron-variant | Wdr60 | Mm_Celera | 12:116224756 | CCATTAGATCACAGG[A/T]GTGTACTACAAATGC | 217935 |
rs51628344 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Wdr60 | Mm_Celera | 12:116218589 | CTGTATGGATGGCTG[G/T]ATGGATGGCTGTGCA | 217935 |
rs51644829 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116225567 | AGAATTCAAGGCCAG[G/T]CTGGGTTACATGCTT | 217935 |
rs51646945 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116223603 | ACACATACAACACAT[A/C]CATAAGTAAATAAGT | 217935 |
rs51669088 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116236966 | AAATTTAAATTCTCA[A/G]GCTGGAGAGATACCT | 217935 |
rs51685720 | snp | A/T | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116263133 | TTGAGTTTCTTTGTC[A/T]GATCCTTCTTTGACC | 217935 |
rs51689050 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116212091 | AACATAAAGACATAT[C/T]ATTAAACCTATCCTC | 217935 |
rs51691140 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116214124 | ATCACATACTTGATC[A/G]GTTCTGCAGATCCAC | 217935 |
rs51707956 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116210406 | CAATGGACTGTTTTG[G/T]TTTTTTTTTTGTCTT | 217935 |
rs51715564 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116226313 | ATCCCAGGTGTTATG[C/T]ACGCTAGGAAAGCAT | 217935 |
rs51722368 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Wdr60 | Mm_Celera | 12:116247272 | ATTCTGATTCAAACT[A/G]CTTTGTAATTGGATC | 217935 |
rs51724065 | snp | A/G/T | 0.459184 | 0.136902 | intron-variant | Wdr60 | GRCm38.p3 | 12:116248692 | TGACACGTGCTGCCA[A/G/T]TGTGTATTACAGTGA | 217935 |
rs51732946 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116252126 | TATTACAGTGACATG[A/T]GCTGCCTGTGTGTAT | 217935 |
rs51742955 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116228745 | TGCTGGGCACCACTC[A/G]CTCCTGCCAAGTCTT | 217935 |
rs51790638 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116210780 | AAACTATTTTTAATT[A/T]AAAAAAAAGACCCCA | 217935 |
rs51798208 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Wdr60 | Mm_Celera | 12:116213824 | CATGGCCTTTACAAA[A/G]TGACAAGCCACTCCT | 217935 |
rs51837591 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr60 | Mm_Celera | 12:116239415 | AGAGCAGAAGGTCCT[C/T]ACTCTGTGTCTGGGT | 217935 |
rs51841705 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116232929 | ACAATCCCTGGGCTT[A/G]GGTCCTGAACTGTAT | 217935 |
rs51857786 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116213055 | AGGGGCTTGTGGTCT[A/C]AGGAAGGAATGGTGA | 217935 |
rs51865640 | snp | A/T | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235787 | GCACTCGGGAGACAG[A/T]GGCAGGTGGATTTCT | 217935 |
rs51892730 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr60 | Mm_Celera | 12:116230477 | AACCTGTCACTGCCG[C/T]AGAAGCCAAGCAAGC | 217935 |
rs51899644 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116223507 | TCAGAGTTCAATTCC[C/T]AGCAACCACATGGTA | 217935 |
rs51909872 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116208608 | ATCCTTCCCAGACCA[G/T]CAGGAAGTGTCTGAC | 217935 |
rs51925341 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116257111 | AATAAATAAATCCTT[A/T]AAAAAGATAATGAAC | 217935 |
rs51940587 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Wdr60 | Mm_Celera | 12:116245304 | AAATACACTGCCTTG[C/T]CACTCTGAGGCCATA | 217935 |
rs51946272 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Wdr60 | Mm_Celera | 12:116224266 | ACACTTAGAAGAAGT[C/T]GTACGGGTGTGAAAT | 217935 |
rs51982350 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116213858 | AGCTCCCTCCAATGA[A/G]GAGCCGCTCCTATCA | 217935 |
rs51989759 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | Mm_Celera | 12:116252371 | ATCTGACTTAAAAAT[C/T]GTCTAAATTCCTCTG | 217935 |
rs52031070 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Wdr60 | Mm_Celera | 12:116228140 | ATCTCTCTTTCTCAG[A/C]CTCACTCTCCTTCTT | 217935 |
rs52038868 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116252130 | ACAGTGACATGAGCT[G/T]CCTGTGTGTATACAG | 217935 |
rs52041390 | snp | C/T | 0.35503 | 0.226867 | downstream-variant-500B | Wdr60 | Mm_Celera | 12:116206123 | ATCTGCACATGCCTG[C/T]ATGTATGTCCTGTGC | 217935 |
rs52042272 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116223329 | AAGCATGCCTGTAAT[C/T]TCACCACTTGAGAGG | 217935 |
rs52082110 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Wdr60 | GRCm38.p3 | 12:116249173 | TGTGCTGCTTGTGTG[C/T]ATTATAGTGACATGT | 217935 |
rs52097762 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wdr60 | Mm_Celera | 12:116232507 | ATACTTAAAACCTCA[C/T]CAAAAACAACACTGG | 217935 |
rs52107077 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Wdr60 | Mm_Celera | 12:116229179 | AGATAAAAATTCAAA[A/T]TTGACTCTGCAAATG | 217935 |
rs52112484 | snp | A/G | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116229100 | aaccataaatagata[A/G]atagatagatagata | 217935 |
rs52130450 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | GRCm38.p3 | 12:116250025 | TGCCTGTGTGCATTA[C/T]AGTGACATGTGCTGC | 217935 |
rs52134557 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr60 | Mm_Celera | 12:116248349 | AGGGTCACAACACAC[A/G]CTGCTGCCTGCGTGC | 217935 |
rs52137205 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116210607 | GTTTTTGTCTTATTC[A/T]GGTTTGTTTCTTTTT | 217935 |
rs52138877 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Wdr60 | Mm_Celera | 12:116247281 | CAAACTACTTTGTAA[C/T]TGGATCACTTAATTT | 217935 |
rs52140653 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Wdr60 | Mm_Celera | 12:116250956 | TGACATGTGCTGCCA[G/T]TGTGTATTACAGTGA | 217935 |
rs52146670 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116237218 | TTGTAGACGTTGATT[C/T]TCTCCTAATTTCTTC | 217935 |
rs52150531 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116210574 | TTTTGTCTTTTCTTT[A/G]GCTCTTTCCATTTGT | 217935 |
rs52162959 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116212239 | CGGGATGTAAAGTGA[A/G]TAAGTAAAAAAAAAA | 217935 |
rs52170625 | snp | C/T | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116236153 | ACATACATACATACA[C/T]ACATTCATACATTCA | 217935 |
rs52201647 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Wdr60 | GRCm38.p3 | 12:116251922 | TGTGCTGCCTGTGTG[C/T]ATTATAGTGACATGT | 217935 |
rs52226833 | snp | C/G | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116248397 | TGCCTGTGTGTATTA[C/G]AGTGACATGTGCTGC | 217935 |
rs52240311 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr60 | GRCm38.p3 | 12:116250020 | TGTGCTGCCTGTGTG[C/T]ATTATAGTGACATGT | 217935 |
rs52244395 | snp | A/T | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235850 | GTTCCAGGACAACCA[A/T]GACTATATAGAGAAA | 217935 |
rs52248107 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116237903 | TATATATATATATAT[A/G]TATGTATATATATAT | 217935 |
rs52258603 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116210600 | TTTGTTTGTTTTTGT[C/G]TTATTCTGGTTTGTT | 217935 |
rs52267318 | snp | A/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116250823 | TGCTGCCTGTGTGTA[A/T]TACAGTGACATGTGC | 217935 |
rs52269557 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116237187 | GGGGAGAGAGAGAAA[A/G]AGAGAGAGACAGAGA | 217935 |
rs52270473 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116252088 | TGCCTGTGTGCATTA[C/T]AGTGACATGTGCTGC | 217935 |
rs52277181 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116222908 | TCTGAAGTCAGCTAC[A/G]GTGTACTTAAGAAAT | 217935 |
rs52277789 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116261227 | TCACTGTAAAAGAGG[C/T]GGCTTACCCCTCCTC | 217935 |
rs52277832 | snp | A/T | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116236158 | CATACATACACACAT[A/T]CATACATTCATACAC | 217935 |
rs52289158 | snp | C/T | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116236139 | CACTCTGTatacata[C/T]atacatacatacaca | 217935 |
rs52293963 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116248217 | CTTCTCCCGATCTGC[A/G]TCTTTGGCTTTCCTG | 217935 |
rs52313772 | snp | A/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116249119 | TGCTGCCTGTGTGTA[A/T]TACAGTGACATGTGC | 217935 |
rs52329517 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116242438 | AGAACCCACAAGATG[G/T]AAAGAAAGAAGCAAC | 217935 |
rs52336158 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116261220 | GCCTGACTCACTGTA[A/G]AAGAGGCGGCTTACC | 217935 |
rs52344488 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116248247 | GTGCTTCTTCTCGCC[A/G]TCCTCCTTGTACAGC | 217935 |
rs52348835 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116210611 | TTGTCTTATTCTGGT[G/T]TGTTTCTTTTTATAT | 217935 |
rs52366750 | snp | C/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116252104 | AGTGACATGTGCTGC[C/T]TGTGTGTATTACAGT | 217935 |
rs52367011 | snp | A/C | | | intron-variant, upstream-variant-2KB | Wdr60 | GRCm38.p3 | 12:116235911 | AAGAAAAAAACAAAA[A/C]AACAACAACAACAAC | 217935 |
rs52387410 | snp | C/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116249166 | AGTGACATGTGCTGC[C/T]TGTGTGCATTATAGT | 217935 |
rs52392817 | snp | C/T | 0.5 | 0 | intron-variant | Wdr60 | GRCm38.p3 | 12:116249150 | TGCCTGTGTGCATTA[C/T]AGTGACATGTGCTGC | 217935 |
rs52401723 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116255683 | ttcacacaggagcgc[A/G]cacacacacacacac | 217935 |
rs52409658 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr60 | GRCm38.p3 | 12:116248360 | ACACGCTGCTGCCTG[C/T]GTGCAATACAGTGAC | 217935 |
rs52417104 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116212156 | ATACCCCCACCAGCT[A/C]AGAGGAGAAGGGGAG | 217935 |
rs52418369 | snp | A/T | 0.5 | 0 | intron-variant | Wdr60 | Mm_Celera | 12:116224350 | ACATACACATGCAGG[A/T]ATGTACTTATGGAAA | 217935 |
rs52435678 | snp | A/G | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235862 | CCAAGACTATATAGA[A/G]AAACCCTGTCTCGAA | 217935 |
rs52436446 | snp | A/G | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235852 | TCCAGGACAACCAAG[A/G]CTATATAGAGAAACC | 217935 |
rs52465481 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116229078 | ACTGAGAGAGTGTGT[C/T]TTGAAAAACCATAAA | 217935 |
rs52467791 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116237907 | TATATATATATGTAT[A/G]TATATATATATGAGC | 217935 |
rs52486513 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116229185 | AAATTCAAATTTGAC[C/T]CTGCAAATGAAGTTT | 217935 |
rs52502970 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Wdr60 | Mm_Celera | 12:116247304 | CTTAATTTCTCCTTT[A/C]AAAGTAGCACCTACC | 217935 |
rs52521709 | snp | C/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116249178 | TGCTTGTGTGCATTA[C/T]AGTGACATGTACTGC | 217935 |
rs52523650 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116212230 | GACAGTGAACGGGAT[A/G]TAAAGTGAGTAAGTA | 217935 |
rs52544566 | snp | A/C | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235929 | CAACAACAACAACAA[A/C]AAAAAAAACAGAATT | 217935 |
rs52544578 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Wdr60 | GRCm38.p3 | 12:116250107 | TGTGCTGCCTGTGTG[C/T]ATTATAGTGACATGT | 217935 |
rs52553761 | snp | C/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116249026 | AGTGACATGTGCTGC[C/T]TGTGTGCATTATAGT | 217935 |
rs52574086 | snp | A/G | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116229096 | gaaaaaccataaata[A/G]atagatagatagata | 217935 |
rs52582845 | snp | A/T | 0.32 | 0.24 | intron-variant | Wdr60 | GRCm38.p3 | 12:116248552 | AATGACATGTGCTGC[A/T]TGTGTAATACAGTGA | 217935 |
rs52584291 | snp | C/G/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116249038 | TGCCTGTGTGCATTA[C/G/T]AGTGACATGTGCTGC | 217935 |
rs52586387 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Wdr60 | Mm_Celera | 12:116232497 | CCACAGTCATATACT[A/T]AAAACCTCATCAAAA | 217935 |
rs107660966 | snp | A/C | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116208064 | AAAACCAAAAAAAAA[A/C]AAAAAAAAAAAAAAA | 217935 |
rs107726476 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116240314 | TTTTGGTTTTTTGGT[G/T]TTTTTTTGTTTGTTT | 217935 |
rs107995440 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116208063 | AAAAACCAAAAAAAA[A/C]AAAAAAAAAAAAAAA | 217935 |
rs108250549 | snp | C/T | 0.432528 | 0.170832 | intron-variant | Wdr60 | GRCm38.p3 | 12:116249306 | TGTGCTGCCTGTGTG[C/T]ATTATAGTGACATGT | 217935 |
rs108324945 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116232135 | AAAATTTTTTTTTTA[A/T]AAAAAAGGTCAATGA | 217935 |
rs108425190 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116208057 | TCTCAAAAAAACCAA[A/G]AAAAAAAAAAAAAAA | 217935 |
rs108493967 | snp | C/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116248867 | ACTGCTTGTGTAATA[C/T]AGTGACACGTGACAC | 217935 |
rs108738350 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116237578 | CAGGACAGCCAGGGC[A/T]ACACAGAGAAACCCT | 217935 |
rs108787456 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116251927 | TGCCTGTGTGCATTA[C/T]AGTGACATGTGCTGC | 217935 |
rs211729092 | snp | A/G/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116260717 | AAAACTACATACTGA[A/G/T]GAGAAGGTTGACTAT | 217935 |
rs211730108 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116253166 | TTTTTAAAGTAAACT[C/G]AAGACTAGCCACTAG | 217935 |
rs211732218 | in-del | -/A | | | intron-variant | Wdr60 | Mm_Celera | 12:116238464 | TATTTATTCACTTAT[-/A]ATACTCTTTCAATTA | 217935 |
rs211782177 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116253624 | AGGACCCAAGGAGCT[A/G]AAGGGGTCTGCAACC | 217935 |
rs211782687 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116242986 | CGCAGGATACTCATG[G/T]ACATAAAATAAAAAT | 217935 |
rs211839815 | in-del | -/CACTCTGTGTCAGA | | | intron-variant | Wdr60 | Mm_Celera | 12:116239414 | AGAGCAGAAGGTCCT[-/CACTCTGTGTCAGA]CACTCTGTGTCTGGG | 217935 |
rs211855761 | in-del | -/TATTATTATTATTATTAT | | | intron-variant | Wdr60 | Mm_Celera | 12:116210629 | TTCTTTTTATATTAC[-/TATTATTATTATTATTAT]TATTATTATTATTAT | 217935 |
rs211955143 | in-del | -/CT | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116238467 | TATTCACTTATAATA[-/CT]CTCTTTCAATTATCT | 217935 |
rs211970712 | snp | C/T | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235618 | TTTCCATTCAGGAGT[C/T]AGCATCCTCTTCTGC | 217935 |
rs211986029 | in-del | -/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116214880 | AGGTTGATAATCCTA[-/T]TATCACAAAAATAAC | 217935 |
rs212014181 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116226773 | GAATTTTGTAGTCAA[C/T]AAAGACAGGGTTAAT | 217935 |
rs212015646 | in-del | -/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116213843 | AAGCCACTCCTATCA[-/G]GCTCCCTCCAATGAG | 217935 |
rs212112713 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116232395 | AGACTAGGGTTCAGG[C/T]CAATTTAATGATTCC | 217935 |
rs212175587 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116233147 | TATCATGCCCCAAGA[A/G]GCTATGTTAGACTTT | 217935 |
rs212246094 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116224655 | TATCTGATATGTAGG[C/T]TCTCTGATATGTGAC | 217935 |
rs212253999 | in-del | -/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116232113 | CATATAGAAAATTCC[-/T]TTTAAAAAAATTTTT | 217935 |
rs212340266 | in-del | -/GCT | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235454 | CATTGGGCTGTCTGG[-/GCT]GCCCGGCAGTGTCTG | 217935 |
rs212373395 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Wdr60 | GRCm38.p3 | 12:116206824 | AGTCCCAGCCTTGGA[C/G]TCCTAGCCCTGTACT | 217935 |
rs212456950 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116224076 | TGATCTCTCAGCCAG[C/T]GGGACTTCAGCTCCT | 217935 |
rs212528717 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116215461 | TTCTAGACCCAACTA[A/G]TCCCCTTCTTCAGGC | 217935 |
rs212572404 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116229237 | CTGACTCCAGGCTTT[C/G]TTTGTTTACCATTTC | 217935 |
rs212592674 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116220210 | GCAGTCTTCTAGAAA[G/T]GATGTCAACTACAAA | 217935 |
rs212652638 | in-del | -/AAA | | | intron-variant | Wdr60 | Mm_Celera | 12:116254316 | AGTTAAAAATGAATT[-/AAA]TAAAAAAAAAAAAAA | 217935 |
rs212733465 | snp | G/T | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264046 | TGATTAGAAGCTTCT[G/T]TAATGAGCAGAGCAC | 217935 |
rs212752120 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116260263 | CCATGTAGAGAAGGA[A/G]AGGAGACCCACATTG | 217935 |
rs212777798 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116214042 | CAGGCTGCCGCCAAT[A/G]AGGAGCCACTCCTAT | 217935 |
rs212849551 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116236251 | GCTAAACCTCAGGGG[-/AA]AAAAAAAAAACACAA | 217935 |
rs212855752 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116218326 | AGTGACAAATGTATT[A/C]ATTCTTTTATCTTAG | 217935 |
rs212858319 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116257258 | TGCAGGACTGTACCC[C/T]AAAATTTTCCAGAAG | 217935 |
rs212889115 | in-del | -/ACACCAGAGGAT | | | intron-variant | Wdr60 | Mm_Celera | 12:116260749 | CATACACCAGAGGAC[-/ACACCAGAGGAT]TTAAGGATTAAACAA | 217935 |
rs212961047 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116209178 | AGAAGGTATAAAGGC[A/G]GGGATATGGGAGATA | 217935 |
rs213030096 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116261798 | CACACACAAATATCC[C/T]ACCCAAACTCTAAAG | 217935 |
rs213087602 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116255047 | TTTGGTAGAATACTT[C/T]TATTAAAGTGCTTTA | 217935 |
rs213125529 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116212255 | TAAGTAAAAAAAAAA[A/T]TTTTTTTTAATTTTT | 217935 |
rs213143973 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116245158 | CAAAATCATAGTTCT[A/T]CCTTTCTAGGGAGCA | 217935 |
rs213407837 | snp | C/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116236619 | GAGTTTATAAATTTG[C/T]TCCAAGAATAATTTT | 217935 |
rs213480288 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116254385 | CAAGTGCTCTGCTGA[A/C]TTGGGCCTGCAAGCC | 217935 |
rs213508940 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116219354 | GGAAAGTGCTGCTCA[C/T]GGGCAACTGATAAGG | 217935 |
rs213559630 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116210711 | ATGGATCAGGAGGTA[G/T]ATCGAGTCAGGGAGA | 217935 |
rs213751427 | snp | A/T | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116263916 | GTTATCACTTTAACG[A/T]GCAGTATATATTTGA | 217935 |
rs213819445 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116218206 | ACATTTTATCACCAT[A/G]AAACAATCTACACAA | 217935 |
rs213819548 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116208331 | GTGAGGGTTTCCCAG[C/T]ATCTCAGGCCACCAA | 217935 |
rs213840360 | in-del | -/AAA | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116219729 | CCCACATAGAAATTG[-/AAA]AAAAAAAAAAAAAGA | 217935 |
rs213849480 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116227054 | CACATATGTCCAAGT[C/T]AGAGGACAACCTTAT | 217935 |
rs213878660 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116208941 | AGCCCAAGCTGGCCT[C/T]AAAGTTGTAATCCCC | 217935 |
rs213897071 | snp | A/C/G | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116253677 | AACTAACCAGTACCC[A/C/G]CCAGAACTGTGTCTC | 217935 |
rs213954029 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116254317 | AGTTAAAAATGAATT[A/T]AAAAAAAAAAAAAAA | 217935 |
rs214003135 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116244027 | CATGCCATGGACATC[A/T]GTATGCCAACTACAA | 217935 |
rs214088917 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116220195 | ACTCACACGTCATAC[A/G]CAGTCTTCTAGAAAT | 217935 |
rs214121789 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116261611 | TGTTCATAAAAGAAA[A/C]ACTACTACAGATAAA | 217935 |
rs214127801 | snp | A/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116249403 | TGCATTATAGTGACA[A/T]GTGCTGCCTGTGTGT | 217935 |
rs214177148 | in-del | -/ATGTGTATGTGTATGTGTATGTGTATGTGTATGTGTATGTGTATGTGTATGTGT | | | intron-variant | Wdr60 | Mm_Celera | 12:116224291 | GAAATGCTTGCTCTT[lengthTooLong]TGTGTATGTGTATGT | 217935 |
rs214337802 | in-del | -/TGCA | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116208485 | CCCTGTGTGCCCTCT[-/TGCA]GCCATTGCCCTACCA | 217935 |
rs214378264 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116240808 | GCCACTACGGTTAAG[C/T]ATCCCTGGTCACAGC | 217935 |
rs214424275 | in-del | -/TCTTT | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116210458 | TTATCAGGGCTTCAC[-/TCTTT]TTTTTTTTTTTTTAC | 217935 |
rs214430584 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116261009 | GTATTCCAAGCAAAT[C/G]GGCCCACGAAAAAAG | 217935 |
rs214518829 | in-del | -/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116229988 | TTAAAACACTAACAG[-/C]ATGCTATCCTTTGGT | 217935 |
rs214589423 | in-del | -/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116241979 | TATCCTACTTACTCT[-/G]GGGGGGGGAAAAAGC | 217935 |
rs214640443 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116238512 | TAAACATTTCAACAT[A/G]GACCCTTGCCCTACT | 217935 |
rs214663345 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116254899 | CAGACACACCAGCTT[C/T]CACTGACACCTCATT | 217935 |
rs214703370 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116221977 | GGCAGTGATGGTGCA[C/T]GCCTTAATCCCAGGA | 217935 |
rs214704637 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116239590 | ATTTTGCAGTAGAGT[C/T]CTAAAATTTCTTGTT | 217935 |
rs214742827 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116251838 | TGTGCTGCCTGTGTG[C/T]ATTATAGTGACATGT | 217935 |
rs214821183 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116256275 | GCACAGAAGACCCTC[C/T]GTCACTATGAAAGCA | 217935 |
rs214828828 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116220233 | ACTACAAAGAGAACA[C/T]ACCTGAGCTACAGCA | 217935 |
rs214894307 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116221155 | CCTTAACAGGTGCTT[C/T]ACCAAAGAAGACACA | 217935 |
rs214972701 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116258594 | GTCACCATGTGCAAG[A/C]CCCAAACCCACATCT | 217935 |
rs214991566 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116210459 | TATCAGGGCTTCACT[C/T]TTTTTTTTTTTTTTT | 217935 |
rs215040699 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116247876 | GATGCTTCGTCATGG[C/T]AACCAAAAGCGCTCA | 217935 |
rs215056669 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116257352 | TATGTAGGGCTGTGA[A/G]CCTGGTCACTGTCCA | 217935 |
rs215110154 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116230476 | TAACCTGTCACTGCC[A/G]TAGAAGCCAAGCAAG | 217935 |
rs215176983 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116221222 | TCCAGTGTCACCATA[A/T]GGAGCCACTTCAACC | 217935 |
rs215279974 | in-del | -/G | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116243162 | GGCCATGAAGATGCA[-/G]GAGTAGTCTAGTATA | 217935 |
rs215318457 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116255142 | AAAAACACTAATAAA[A/T]ACTAGTTTCCTTTGT | 217935 |
rs215379195 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116255824 | AGTCCATGATGCAGA[G/T]ACACACCTTTCTTTT | 217935 |
rs215448274 | snp | A/C | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264756 | AGACAGAACAGCATC[A/C]GTATCCTACCCTTCC | 217935 |
rs215543706 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116229422 | TTAAGAAAAGAATAC[A/T]CCCCATGTATTTGCA | 217935 |
rs215719768 | in-del | -/GCTGTATGGATG | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116218573 | CCGTGGGTTCACTCT[-/GCTGTATGGATG]GCTGTATGGATGGCT | 217935 |
rs215732834 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116252978 | AAGACCCATAACAAA[A/G]CCCAAACAACTATTA | 217935 |
rs215971230 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116247856 | TCCTCCCTTGACTTA[A/T]GGCTGATGCTTCGTC | 217935 |
rs215981957 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116227117 | AATTGAACTCAGATT[A/G]CCAGTCATACATATC | 217935 |
rs216111535 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116237430 | ACTAAATTTCTATCA[C/G]CAAAAAATAAGTGTG | 217935 |
rs216181599 | in-del | -/TGA | | | intron-variant | Wdr60 | Mm_Celera | 12:116210774 | TAAAAAAACTATTTT[-/TGA]TAATTTAAAAAAAAG | 217935 |
rs216219462 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116214321 | CAGTGAGTTCCACTG[G/T]GATGACAGTTCTTAC | 217935 |
rs216219509 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116223898 | CAGCAGTGAAAAGCC[C/T]CAAATGACATGTGTG | 217935 |
rs216269524 | snp | A/C/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116215363 | CAACCATAGTGACTA[A/C/T]ACATTCAAGTAAATG | 217935 |
rs216317347 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116207238 | CAATTTCTCTTACTT[C/T]AGATATATGTACATC | 217935 |
rs216325172 | snp | A/G | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116263782 | CAGACCCTGGTCTGC[A/G]TGCTTGCATGACAAA | 217935 |
rs216418495 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116258926 | AAAGTGTGAGGAGCC[A/G]GTGAAATGAGGGCAC | 217935 |
rs216475307 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116259660 | CATACAGAACACCCA[C/T]AATATAAAAGCTAGA | 217935 |
rs216560783 | in-del | -/ACACACACAC | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116236169 | CATTCATACATTCAT[-/ACACACACAC]ACACACACACACACA | 217935 |
rs216654767 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116238226 | CCATGTATTTTCAAC[C/T]TTTCTGTGTCTGGCA | 217935 |
rs216659023 | snp | A/T | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116234995 | TGTAGCTAGTAAAAT[A/T]TTTTTTCCAATACAT | 217935 |
rs216692650 | in-del | -/C | | | upstream-variant-2KB | Wdr60 | GRCm38.p3 | 12:116263215 | TTGAACAAGGCTTTG[-/C]CTCCTCAACTCACAC | 217935 |
rs216742071 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116257822 | GCATCCTTAGAAGCA[G/T]AGGGATACTCTGTCT | 217935 |
rs216781668 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116238601 | TATCTAGCTGCAAGG[A/G]CCTGACAATGACTTA | 217935 |
rs216889491 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116231638 | CACAAGGACAACACA[G/T]TGAACCCTGAGCGCT | 217935 |
rs217072393 | snp | C/T | | | intron-variant, utr-variant-5-prime | Wdr60 | Mm_Celera | 12:116234315 | CTCCCTACAATCCAG[C/T]CTCGAGATTTCCTGC | 217935 |
rs217085659 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116254204 | ACAAAATGATACACA[C/T]ACCAATCATCCTATT | 217935 |
rs217140280 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116224850 | TAAACCTTCAGTCTG[C/T]CAAGGCTTTTCTAGA | 217935 |
rs217258272 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116218396 | ACAAGTCCTAACATA[G/T]CATCTAGCACTGATG | 217935 |
rs217260034 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116227942 | CAGCATACTACAGAT[A/G]TCACAAATGAATGAA | 217935 |
rs217299638 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116219200 | TACATGTACAGGGTT[A/T]GGAAGAAAGTCAAAA | 217935 |
rs217381438 | in-del | -/A | | | intron-variant | Wdr60 | Mm_Celera | 12:116222942 | AATAAATCTAAAAAG[-/A]AAAAAAAAAGTAAAC | 217935 |
rs217388915 | in-del | -/AC | | | intron-variant | Wdr60 | Mm_Celera | 12:116210377 | AGCAGATATGGAAGA[-/AC]CACAACAAACCCAAT | 217935 |
rs217463287 | snp | C/G | | | intron-variant, utr-variant-5-prime | Wdr60 | Mm_Celera | 12:116234243 | CAGAGGCCTCACAAC[C/G]ACTGTCACTCTTACA | 217935 |
rs217661536 | snp | A/G | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116241987 | TTACTCTGGGGGGGG[A/G]AAAAAGCAAAACCTC | 217935 |
rs217712444 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116233711 | TAGTGGTGGGAGTAT[A/G]TCATGAGCCAGTGTG | 217935 |
rs217719928 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116247983 | CATAAAGACAATCCC[A/G]TGGAGCAATACCTTC | 217935 |
rs217726632 | snp | C/G | | | downstream-variant-500B | Wdr60 | Mm_Celera | 12:116206138 | TATGTATGTCCTGTG[C/G]GTGTGCTCATGTGTC | 217935 |
rs217734752 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116260835 | TATAAATACTGCTCA[C/T]TAAGAACTCTCAACA | 217935 |
rs217766229 | snp | A/G | | | intron-variant, utr-variant-5-prime | Wdr60 | Mm_Celera | 12:116234409 | CAGGGCTCAGCTTTC[A/G]GTTTCCACACCTTTC | 217935 |
rs217907687 | in-del | -/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116259124 | AGGCCCTCCATCCCC[-/T]AGGGCTTCAGCCTTC | 217935 |
rs217965352 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116260404 | AATTCCCTACAACAC[A/G]TAATAATCAAAACAC | 217935 |
rs217992403 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116242480 | GCCCTTTGACCCTAA[C/T]ATGAACACCATTACA | 217935 |
rs218009686 | in-del | -/A | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116253408 | AAAAAAAAAAAAAAA[-/A]AAAGACGAAGAAGAA | 217935 |
rs218102144 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116214566 | TTCAACTAGGGGTGA[A/T]ACTTTCTAAATTTTC | 217935 |
rs218103516 | snp | A/C | | | downstream-variant-500B | Wdr60 | Mm_Celera | 12:116205888 | ACTTACTCAGTGGCT[A/C]TGTGCCAGTCACATA | 217935 |
rs218110911 | in-del | -/TTT | | | intron-variant | Wdr60 | Mm_Celera | 12:116213203 | GTCAATTTAATTTAG[-/TTT]TTTTTTTTTTTGTTA | 217935 |
rs218131628 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116207931 | GCAGTGGTGGCGCAC[A/G]CCTTTAATCCCAGCA | 217935 |
rs218158191 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116206306 | GAGTTGCTGGAGGGG[C/T]AGTTACACAAGGATG | 217935 |
rs218211976 | in-del | -/A | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116208196 | TCCACCACTTCACAC[-/A]AGTGTGACATTCCTA | 217935 |
rs218234548 | in-del | -/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116257952 | GCTACTATTACCAAA[-/T]TTAAAAAAAAAGCAA | 217935 |
rs218513148 | in-del | -/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116255166 | CCTTTGTTGACTGAA[-/T]TTTTTTTTAAAGTTC | 217935 |
rs218630058 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116262219 | AAAGAGTAGATGGCA[A/C]AAAAAAAAAAAAATC | 217935 |
rs218659973 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116237060 | AGTGGCTCACAACCA[A/T]CTAGACTGGGATCTG | 217935 |
rs218670670 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116243370 | CTTACAAGCTAAACT[C/T]AATCTTAAGGATGCA | 217935 |
rs218685119 | snp | C/T | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116263150 | ATCCTTCTTTGACCC[C/T]CACAGTTGACAACGA | 217935 |
rs218729742 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116261062 | TGGCAAAGGAGAGTT[A/C]AAGCCAAAACTAACC | 217935 |
rs218756270 | snp | A/G | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235250 | GTAAGGTGATGGATG[A/G]CATAAATTAATGTTA | 217935 |
rs218792448 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116243852 | GAGTTTAACAAGAGT[A/C]TAAGACACAGACCTG | 217935 |
rs218886738 | snp | C/T | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235674 | TAGAGCATTTGGACC[C/T]CAGATCTAAGGGTCA | 217935 |
rs218974625 | in-del | -/GCACAGATACCATGGGA | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116230417 | ACAGAGATGTGCCAT[-/GCACAGATACCATGGGA]GCACAGACACCATGG | 217935 |
rs219090809 | snp | C/G | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235376 | AGCCTTGTCATTCTT[C/G]ACATGTCAGGAAACA | 217935 |
rs219117517 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116217967 | CCAATAGCTGATAAA[G/T]TATACAATATACAAC | 217935 |
rs219142476 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116226378 | GCCAGTCTTCCTCCA[C/T]GCCTACAGCCTAAAC | 217935 |
rs219142538 | snp | A/G | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235783 | CCCAGCACTCGGGAG[A/G]CAGAGGCAGGTGGAT | 217935 |
rs219173174 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116218689 | CATTTCTAACGAAAG[A/C]AGAAACAAAGTGAAG | 217935 |
rs219199504 | snp | A/C | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116227294 | CTCTCTCCGCCCCCC[A/C]ACCTCTCCTCAATGC | 217935 |
rs219308876 | in-del | -/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116208056 | TCTCAAAAAAACCAA[-/G]AAAAAAAAAAAAAAA | 217935 |
rs219337925 | in-del | -/AAAAAAAC | | | intron-variant | Wdr60 | Mm_Celera | 12:116261733 | TAAAAAAGCAAATGA[-/AAAAAAAC]AAAAACAAAACAAAC | 217935 |
rs219384885 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116207657 | GCTATGCTCGTCTAC[C/T]GCTGGGGTGGTCCAC | 217935 |
rs219396693 | in-del | -/AAC | | | intron-variant | Wdr60 | Mm_Celera | 12:116246821 | ACAAACAAACAAACA[-/AAC]AAAAAAGTCAATCAT | 217935 |
rs219542275 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Wdr60 | GRCm38.p3 | 12:116206794 | GGACTCCTAGCCCTC[A/G]ACTCCTAGCCCTGGA | 217935 |
rs219543026 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116217726 | GACAGCCACACTTAG[C/T]GCACTCATGTGCACT | 217935 |
rs219729962 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116253275 | GGCGCACGCCTTTAA[A/T]CCCAGCATTTGGGAG | 217935 |
rs219782625 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116243028 | ATAACACTTAGGCCA[C/T]GCAGGCTTGAGCAGG | 217935 |
rs219818112 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116224334 | GTTTGTACATGCATA[C/T]ACATACACATGCAGG | 217935 |
rs219839138 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116243455 | GGAGTCCAGTGTTTT[A/G]GGGGAAACGAGGTAG | 217935 |
rs219908092 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116216110 | TGAGTGGGTTGAAGA[A/G]CAGAGGGAGAGGGGA | 217935 |
rs219936919 | in-del | -/AAG/AAGAAGAAGAAGAAGAAGAAGAAG/G/GAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAA | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116225616 | AAAAAGGAAGAGGAA[lengthTooLong]AAGAAGAAGAAGAAA | 217935 |
rs220020331 | snp | A/G | | | missense, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116246049 | CAACCTTGCTTCTGA[A/G]ACATTTTCAAAGATA | 217935 |
rs220134492 | in-del | -/AA | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116209251 | TATAGTGAAAACTTT[-/AA]AAAAAAAAACATGTA | 217935 |
rs220162815 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116222807 | GAGCACTGACTGTTC[C/T]TCTCACGGTCCAGAG | 217935 |
rs220194068 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116237762 | TATCCATAACACAAA[C/T]GCCCTCTTCTGACTT | 217935 |
rs220202892 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116240048 | TTCCATCGCCCCACC[A/G]TAGATGAATGTCCCA | 217935 |
rs220262983 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116217335 | CATGGTCTCAACCAC[A/G]GACACAGTAAACCTG | 217935 |
rs220428791 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116259279 | CGACTGCACTAGGAT[A/G]GGGCTCAGGTCCGAG | 217935 |
rs220433233 | in-del | -/C | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116211669 | GTGGTGTTAAATGTA[-/C]ATTTGAACCTGTAAT | 217935 |
rs220474673 | in-del | -/CGCGCACACACACACACA | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116255680 | ACATTCACACAGGAG[-/CGCGCACACACACACACA]CACACACACACACAC | 217935 |
rs220663513 | in-del | -/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116211589 | GGACCTCTGTGTATG[-/T]TTTGATTTGACTACA | 217935 |
rs220691315 | in-del | -/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116240854 | ATTTAAAAGTTATGG[-/C]CCCCCAGCCACTGCA | 217935 |
rs220711213 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116219444 | TCTTCAACAGGACAG[C/T]CACTATCAGAAGTAC | 217935 |
rs220777429 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116255637 | CACACATTCACACAG[A/G]AGCAGACACACAGAC | 217935 |
rs220819395 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116254580 | TAACTTGCTGCAGGC[G/T]TTACTGTTATTGCAC | 217935 |
rs220822209 | in-del | -/TGTTTT | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116236009 | TACTATGGATTTTTC[-/TGTTTT]TGTTTTTGTTTTTGT | 217935 |
rs220846539 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116256396 | GCAAGATGGAAGGTA[C/G]ATTCTTAGCATACTA | 217935 |
rs220906407 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116245993 | CCCAGTTACAAGTGT[C/T]CCCATGCATACCTGT | 217935 |
rs220934087 | snp | A/C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116252159 | AGTGACACGTGCTGC[A/C/T]TGTGTGTATTATAGT | 217935 |
rs220992800 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116256292 | TCACTATGAAAGCAC[A/G]CACACATGCATTTAC | 217935 |
rs221013156 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116218878 | GCTTCGGTGGTTCAC[C/T]GATGTGAGGATTCCA | 217935 |
rs221035536 | in-del | -/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116243342 | TTCTCCACTACCCTC[-/T]CCCTGTGCCGGACTT | 217935 |
rs221075217 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116245850 | GGACATTACCAAAGG[A/G]AACAAGAACACATGC | 217935 |
rs221097965 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116209874 | AAACTTCCTAATGTC[A/G]TTCTGTTATACCGAT | 217935 |
rs221155086 | snp | C/G | | | missense, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116248067 | ACTTCGGCGCCTCTC[C/G]TCATCATAGTGCAGT | 217935 |
rs221184811 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116253390 | CTGCCTCAAAAAAAC[A/C]AAAAAAAAAAAAAAA | 217935 |
rs221241349 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116227519 | CCAAATGAGGCATCT[C/T]ACCAGCCTGGTACTG | 217935 |
rs221312641 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116228704 | CCAAAGTATGTTTTC[A/G]CTCTGTCTCCTGAAG | 217935 |
rs221317545 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116218962 | AAATCAGCATTATAC[A/C]TAGAAAGATATAGGG | 217935 |
rs221320149 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116255501 | GGGCATAATGTGGTA[A/G]AAAGAGACCCCATCT | 217935 |
rs221352855 | in-del | -/GGGGT | | | intron-variant | Wdr60 | Mm_Celera | 12:116255445 | CCTACAGCAGGAGGG[-/GGGGT]GGGGTAAGGAGAGGA | 217935 |
rs221384295 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116244271 | TCAGTTTCCTATAGT[C/T]GCAGAAAAGGGTAAA | 217935 |
rs221394054 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116219631 | CACAAAGCACAAGAC[A/G]GTGGTCCAATAGGAT | 217935 |
rs221406368 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116245503 | CTGCAGCAGCACACA[A/G]CGTGACTGCCGATTA | 217935 |
rs221519010 | snp | A/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116221372 | TAGGAATGCAGATGG[A/T]GCGGCCACTGACTGA | 217935 |
rs221559937 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116222735 | TGGACTAAGGCCTCT[A/T]ATTATGTACACTGAC | 217935 |
rs221561640 | snp | G/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116212643 | AGATACAATAAATAA[G/T]AAACAATAAATAATA | 217935 |
rs221580490 | in-del | -/AAGTA | | | intron-variant | Wdr60 | Mm_Celera | 12:116223622 | AGTAAATAAGTAAAT[-/AAGTA]CTTTTTTTTTTAAAA | 217935 |
rs221657463 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116258224 | ACAACACACATACAG[A/G]CAAAACACCCATACA | 217935 |
rs221684758 | in-del | -/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116243956 | ATGGAGAGAATATGA[-/T]TTTTGGAGGAGACCA | 217935 |
rs221723206 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116215021 | CACTGGCAGGTATCT[C/T]AAAATATAAGCACAT | 217935 |
rs221734345 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116253854 | GTATAGGGGGCTTTG[A/G]GAGTAGCATTTGAAA | 217935 |
rs221745245 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116258030 | CCACATGTCAGATGT[A/G]GACTAGAAAGATAGC | 217935 |
rs221774387 | snp | C/T | | | downstream-variant-500B | Wdr60 | Mm_Celera | 12:116206257 | AAAAAGAAGCAAAGA[C/T]GGATGAGATGCCGGG | 217935 |
rs221830100 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116215879 | AATTAAAAAATAAAT[A/G]CAATGCATGATATGA | 217935 |
rs221837756 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116243515 | CACTAGAATAAGAAA[A/T]GTAGTGCATAAATAC | 217935 |
rs221863437 | in-del | -/ATAAA | | | intron-variant | Wdr60 | Mm_Celera | 12:116223604 | ACATACAACACATCC[-/ATAAA]ATAAGTAAATAAGTA | 217935 |
rs221866564 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116261247 | TACCCCTCCTCACTC[C/T]CTTCTCTCCTCTTGC | 217935 |
rs221947721 | in-del | -/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116238752 | CATAAACTTACTTTA[-/T]TTTTTTAGTCATTCT | 217935 |
rs221996216 | in-del | -/TT | | | intron-variant | Wdr60 | Mm_Celera | 12:116253149 | CTGACAAGGAGTTAA[-/TT]TTTTTTAAAGTAAAC | 217935 |
rs222049518 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116229603 | AAACGGTAGGCTTGT[A/G]TTCAGTTGAGATGAG | 217935 |
rs222101023 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116230721 | CTTAACATTATTAGG[C/T]TGTTTATGTCTGCTC | 217935 |
rs222104871 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116255323 | CTTTTAAACAAAATA[C/T]AGCCAAGAAAATGGC | 217935 |
rs222203469 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116259949 | CATTCGTGCACACAC[A/G]CAACCAGACAGTTCA | 217935 |
rs222264074 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116251682 | TGCCTGTGTGTATTA[C/G]AGTGACATGTGCTGC | 217935 |
rs222315501 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116257637 | AATAACAAATTTTGC[A/G]TTCTCATTATACTAT | 217935 |
rs222342023 | in-del | -/A | | | intron-variant | Wdr60 | Mm_Celera | 12:116253114 | AAGACTCCTCAAATT[-/A]AAAAAAAGCAACATA | 217935 |
rs222419533 | snp | A/G | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116225597 | TCCTGTCAGAGGGGG[A/G]AAAAAAAAAGGAAGA | 217935 |
rs222443274 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116262075 | ACCTACAGGGCACAA[C/T]GAACACAGTTTGTAA | 217935 |
rs222470485 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116217553 | ACAAACTAGACCATA[A/G]GATCTAATGGGACTG | 217935 |
rs222473795 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116226289 | AAGTTATTCAGTACT[A/G]AGGACTTTATCCCAG | 217935 |
rs222507320 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116254596 | TTACTGTTATTGCAC[A/G]TATGTTCATTAATTT | 217935 |
rs222523734 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116217853 | TGAGGTATGACACAC[A/G]GCAGAAGTAATGCCA | 217935 |
rs222586820 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116232508 | TACTTAAAACCTCAT[C/T]AAAAACAACACTGGG | 217935 |
rs222588251 | snp | C/G | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116222811 | ACTGACTGTTCCTCT[C/G]ACGGTCCAGAGTTCA | 217935 |
rs222694017 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116262065 | ACATAGCCAAACCTA[C/T]AGGGCACAATGAACA | 217935 |
rs222697500 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116253920 | TAAAAAAAGAAAAAA[A/G]AAAAAAAAACAAAGA | 217935 |
rs222703905 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116260360 | TCTATCAAGTTATAA[A/C]AGGTATGCAGAATAC | 217935 |
rs222808119 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116213071 | AGGAAGGAATGGTGA[C/T]TGTTTTGTGGACTGG | 217935 |
rs222930738 | snp | C/T | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235312 | TACCCATTTTGGGTG[C/T]CATTGTGTAATGGAT | 217935 |
rs222996028 | in-del | -/TTTTGT | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116236018 | TTTTTCTGTTTTTGT[-/TTTTGT]TTTTGTTTTGTTTTT | 217935 |
rs223012368 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116256600 | CCTATAATAGAAGGA[C/T]GTAATGAAGATGTAG | 217935 |
rs223063631 | in-del | -/TACA | | | intron-variant | Wdr60 | Mm_Celera | 12:116239722 | CATACATGAATGTGC[-/TACA]TACACTCTTGGTTTG | 217935 |
rs223107733 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116233897 | ATTCTCCTAGCTACA[G/T]CGGCCTATTCCCACA | 217935 |
rs223118104 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116232022 | CAAGCATCTAAAGAT[A/G]AGAAATCTGCAACAC | 217935 |
rs223160832 | in-del | -/AAAAAAAAA | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116208055 | TGTCTCAAAAAAACC[-/AAAAAAAAA]AAAAAAAAAAAAAAA | 217935 |
rs223284136 | snp | A/G | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116262823 | GGGGGCGCGGGCCGG[A/G]CCAGGCTGGGCCCCG | 217935 |
rs223414071 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116229463 | CATTGAGTGTTTCTA[G/T]TTTATAGAAAATAAA | 217935 |
rs223498577 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116220520 | GATCACCAGCCTGAA[C/G]ACCCAGCCTGAAGAA | 217935 |
rs223541424 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116212867 | CATCTGCACAAGGGG[C/T]TAAAGCTCTATACAT | 217935 |
rs223646236 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116228724 | GTCTCCTGAAGGAAG[C/T]ATCACTGCTGGGCAC | 217935 |
rs223723957 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116220002 | TTGGTGGATCCAACA[A/G]CCATGACTAGAAATA | 217935 |
rs223758210 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116253223 | TAGTGAACAGTGGTT[A/C]ATTTCCATAAGTAAA | 217935 |
rs223762393 | in-del | -/ACTCCTAGCCCTCA | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116206837 | GAGTCCTAGCCCTGT[-/ACTCCTAGCCCTCA]ACTCCTAGCCCTGGA | 217935 |
rs223789449 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116240516 | AGTTGATAAAAGCAA[A/G]ATGTTATGTTAATGC | 217935 |
rs223811335 | snp | C/G/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116237197 | agaaaaagagagaga[C/G/T]agagaTTGTAGACGT | 217935 |
rs223848110 | snp | A/C | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264317 | TGCAGTCGCCTAAAT[A/C]TTCACACACTGTTCA | 217935 |
rs223864629 | snp | A/G | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264218 | CAGGTGCTATAGTTG[A/G]ATGTTGGGATAGGTT | 217935 |
rs223875826 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116232200 | CTGTATCTTAGAGAC[C/T]GCTAAACTGCACTGA | 217935 |
rs223878312 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116210881 | ATGGTTCTCTCTTGA[A/G]AACCCTTCCAAATGA | 217935 |
rs223945691 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116208823 | CATGTACTGGGGTGA[C/T]GGGCATGAGCCGCCA | 217935 |
rs223974205 | in-del | -/AA | | | intron-variant | Wdr60 | Mm_Celera | 12:116216364 | GAAAAAAAACAAAAC[-/AA]AAAAAAAGAACGAAA | 217935 |
rs224037021 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116229627 | AGATGAGCTGTCACT[A/G]ATGTTGAGAGCTTTG | 217935 |
rs224122571 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116207062 | TTCCATTCTCAAAAA[A/T]TGTATTTACTTGTAT | 217935 |
rs224154287 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116237981 | AGATTATCTTATCAC[A/G]TCTTTTATTGCATTT | 217935 |
rs224193238 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116238673 | GAAGATATTTATTCT[A/G]TCTAATGTCTAATTC | 217935 |
rs224219156 | snp | G/T | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235635 | GCATCCTCTTCTGCC[G/T]TTGAACATCAGAACT | 217935 |
rs224290368 | snp | A/G | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116236226 | GTCATAAAATTTTGA[A/G]TCAAAGTCTGGCTAA | 217935 |
rs224367053 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116227856 | GTAGTCTATTGGGAT[A/T]CTAAGAAGTTCCCAA | 217935 |
rs224390830 | snp | A/G | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235833 | CTGGTCTACAAAGTT[A/G]AGTTCCAGGACAACC | 217935 |
rs224518652 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116236823 | TCCAGCACACCACAC[A/T]GAAGAAGGTCTGCAA | 217935 |
rs224544806 | in-del | -/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116252800 | ATTTGTCCCCGTAGT[-/C]CCCTGTAGTCCCTGC | 217935 |
rs224642311 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116240304 | GCTGAAGAGCTTTTG[G/T]TTTTTTGGTTTTTTT | 217935 |
rs224670177 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116261288 | GCTTATCCTCTGTCC[C/T]TTCTCTCCCCATTCC | 217935 |
rs224826003 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116208206 | CACACAAGTGTGACA[C/T]TCCTATCTGATGCTC | 217935 |
rs224838385 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116233542 | TGTAAGTAATTAAGA[A/G]TGAGTCTAAAGTATT | 217935 |
rs224839388 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116241132 | GATAGTTTTGCAGGT[A/G]TACATAATACAAGAA | 217935 |
rs224889517 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116217603 | GAACTGAAAGCCATA[C/T]TAAGTGGTCTGAAAA | 217935 |
rs224900577 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116224313 | TGTGTATGTGTGTGT[G/T]CATGTGTTTGTACAT | 217935 |
rs224960961 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116208168 | ACAAACTGTGTAGCT[C/G]CAGATGACAACTTCC | 217935 |
rs225046451 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116242402 | AACTTGCCTACAAGC[C/T]GGACAACCTGATTGA | 217935 |
rs225071559 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116253611 | AGGAGCTAGAGAAAG[C/G]ACCCAAGGAGCTAAA | 217935 |
rs225104236 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116234095 | AAAAGTGTTCTTTAT[C/T]TCTTCCACTTACCAG | 217935 |
rs225209655 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116243683 | TTATTGGGCTGGGAG[A/G]AAAACAGCATCTTAG | 217935 |
rs225285481 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116230925 | GCTATCTATCTTTAG[A/G]CCTCCTGAGAGCCTT | 217935 |
rs225347470 | in-del | -/CTC | | | intron-variant | Wdr60 | Mm_Celera | 12:116215727 | TCCAGTCTGCCTCTA[-/CTC]CTCCTTTCCCACAGA | 217935 |
rs225353037 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116259171 | TCCCCCGTGATCTTC[C/T]CTGTGGCCCCATTTA | 217935 |
rs225441055 | in-del | -/AGAAGAAGAAGAAGAAGAAGAAGAAGAAGA | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116225629 | AAAAGAAGAAGAAGA[lengthTooLong]AATCACAAGAATATT | 217935 |
rs225472056 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116251550 | TGTATTACAGTGACA[C/T]GTGCTGCCTGTGTGT | 217935 |
rs225492311 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116245512 | CACACAGCGTGACTG[C/T]CGATTACTCTTCCAG | 217935 |
rs225705712 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116216570 | AACCAGAAACATGCA[A/C]ATCTCTCAATGTAAG | 217935 |
rs225749881 | in-del | -/TTTAAGACCAAATC | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116246652 | ACATCTGCACTAATT[-/TTTAAGACCAAATC]GTTAAACTGAGAAAA | 217935 |
rs225832112 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116251810 | TGTGCTGCCTGTGTG[C/T]ATTACAGTGACATGT | 217935 |
rs225869166 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116247411 | TAGCAAGCACCAGTA[A/T]TCTAGGCTGATTGGA | 217935 |
rs225965747 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116220630 | TCTGACTGTAGACAT[C/T]GTGTAACCAGTTCTG | 217935 |
rs225970196 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116242322 | ACAGGAAAACAATAT[A/G]AATGTGCCAAAGAGG | 217935 |
rs226040041 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116212068 | TTTTGGCTTGCTCTT[G/T]TTTTCTGAACATAAA | 217935 |
rs226066444 | in-del | -/AAAAAA | | | intron-variant | Wdr60 | Mm_Celera | 12:116262219 | AAGAGTAGATGGCAC[-/AAAAAA]AAAAAAAAAAAAATC | 217935 |
rs226235948 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116245557 | TATTACACTGCACTA[A/G]TAAGTAACTGCTATT | 217935 |
rs226266962 | in-del | -/AAAAAAAAG | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116253409 | AAAAAAAAAAAAAAA[-/AAAAAAAAG]AAGACGAAGAAGAAG | 217935 |
rs226479050 | snp | C/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116221346 | CAGATGGTGCGGCCA[C/T]TGACTGACGGTAGGA | 217935 |
rs226551709 | snp | A/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116212639 | AAAAAGATACAATAA[A/T]TAATAAACAATAAAT | 217935 |
rs226572280 | snp | C/T | | | upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116264527 | TAATTAGATTATACA[C/T]TAATTTATAATTTCA | 217935 |
rs226599026 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116208494 | GCCCTCTGCATGCCA[C/T]TGCCCTACCAAGCTG | 217935 |
rs226602861 | in-del | -/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116258746 | TTAAATTTAAGATGA[-/T]TTTTTTTCATATAAA | 217935 |
rs226733737 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116209098 | TTTCAGATCTTAATA[A/T]AACCTTTACAATCTA | 217935 |
rs226788058 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116210153 | GCACAACAGGCCTGA[C/T]GCATGTGTGAACTCA | 217935 |
rs226833513 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116215678 | CCTATTTACCCCAGA[G/T]AGGGGAGGCTACTAA | 217935 |
rs226840965 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116220065 | AACAGACTTTTCCTG[C/T]TGTTCCCTCAACCCT | 217935 |
rs226915820 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116206870 | CTAGCCCTGGAGTCC[C/T]AGCCTTGGAGTCCTA | 217935 |
rs227035437 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116254831 | GAGGAAACGGAAGCC[G/T]ATTATGCAGTGGCTG | 217935 |
rs227091785 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116244910 | TGGACTGTAGCCTGT[A/T]AATGTACAGCAAATA | 217935 |
rs227198117 | in-del | -/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116226999 | GGTTTCTGCTGTGAC[-/C]GTGTGTGTATGCTTG | 217935 |
rs227213972 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116214727 | ATCTGGCTCAACACC[A/G]AGTTTCCACTTCTAC | 217935 |
rs227417107 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116215150 | GGAGAAATCATGACC[A/T]TGGCAACTCTTATTA | 217935 |
rs227420520 | in-del | -/AA | | | intron-variant | Wdr60 | Mm_Celera | 12:116259046 | AAACAAAAAACAAAC[-/AA]AAAAAAAACAAAAAC | 217935 |
rs227550188 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116226410 | TAAATTCTGTGTCCA[C/T]GGAGACCATGTGGCT | 217935 |
rs227572759 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116242208 | GTATGTGCTCCCTGC[C/T]ACCAATTCAGTCACT | 217935 |
rs227626576 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116220705 | GAGCCAAATAAGAAC[C/T]TTCTTCTTTAATATG | 217935 |
rs227626691 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116211549 | GGGGGTTGCACAACT[G/T]GGGGGAGGGGGTCCA | 217935 |
rs227628073 | snp | C/G | | | missense, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116218139 | GAGATATCTGCTTTT[C/G]GTAATTCAACAACCA | 217935 |
rs227683965 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116212173 | GAGGAGAAGGGGAGA[A/G]AGGATGGGGGAAGGA | 217935 |
rs227706136 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116261339 | CTGTTAATGGCTGCT[C/T]TCTCCCTCTCCCCCT | 217935 |
rs227732567 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116257217 | GACTACCAGACTGGG[C/T]TACACAGAGGACACC | 217935 |
rs227733790 | in-del | -/TTT | | | intron-variant | Wdr60 | Mm_Celera | 12:116212542 | ATAAAACAAAACTTA[-/TTT]GGCGGTTTAGTGAAA | 217935 |
rs227757848 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116254296 | AATTATTACATGTCA[A/C]TAATAAGTTAAAAAT | 217935 |
rs227759893 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116257123 | CTTTAAAAAGATAAT[G/T]AACTAATTAGTTAAT | 217935 |
rs227817258 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116257710 | AGTTTTGCTTCCTAT[C/T]GAAATGAAAGCTGAT | 217935 |
rs227925633 | in-del | -/GGACCAGGCT | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116262821 | ATGGGGGCGCGGGCC[-/GGACCAGGCT]GGGCCCCGCGGCGCA | 217935 |
rs227941311 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116258307 | GCCATAGTAAACTAT[C/G]TCCTCCCAAACACTG | 217935 |
rs227967041 | snp | C/G | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116213847 | CCACTCCTATCAGCT[C/G]CCTCCAATGAGGAGC | 217935 |
rs227990660 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116259588 | ACTAGAACCACTGTC[A/C]ACCAGGAACTCCACA | 217935 |
rs228066168 | in-del | -/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116211590 | GACCTCTGTGTATGT[-/T]TTGATTTGACTACAA | 217935 |
rs228073852 | in-del | -/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116253289 | ACCCAGCATTTGGGA[-/T]GGCAGAGGCAGGCGG | 217935 |
rs228088963 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116251843 | TGCCTGTGTGCATTA[C/T]AGTGACATGTGCTGC | 217935 |
rs228096730 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116247864 | TGACTTAAGGCTGAT[G/T]CTTCGTCATGGCAAC | 217935 |
rs228105805 | in-del | -/AAAC | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116228936 | TGACACAGTGACTCA[-/AAAC]AAACAGTCAGGCTGT | 217935 |
rs228396156 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116230348 | AATTAGCAGAAATGG[G/T]GAAAGGAAGCAAAAG | 217935 |
rs228397541 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116257807 | ATACAGAGTTTGAAG[G/T]CATCCTTAGAAGCAG | 217935 |
rs228430037 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116220972 | ACAGATATAAATATA[A/G]TACAGAGAGAAGAAA | 217935 |
rs228468279 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116221616 | CAGCATGGGTTCCTG[C/T]ACATGGGGCCTGTGA | 217935 |
rs228555362 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116257866 | GAAAGATACAAATAA[A/C]GATTTGTTTAAATTA | 217935 |
rs228734124 | in-del | -/TAAACT | | | intron-variant | Wdr60 | Mm_Celera | 12:116246835 | AAAAAAAGTCAATCA[-/TAAACT]TAAATATTGCAGAGA | 217935 |
rs228759429 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116255807 | GGTTACACTATAGAT[A/G]AAGTCCATGATGCAG | 217935 |
rs228810659 | in-del | -/AAAA | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116237448 | AAAAATAAGTGTGTT[-/AAAA]AAAAAAAAATCAGCT | 217935 |
rs228816495 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116256814 | TCAACAACAATACAG[C/T]CAAGCATGAGTGTCA | 217935 |
rs228919024 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116224467 | TTTATTTTCTTTTCT[C/T]TTGTTTTTTGAGACA | 217935 |
rs229008681 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116254756 | GTTTGTTACTGAGAC[A/G]AGCGGGTAAATGTCT | 217935 |
rs229069475 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116260001 | AAAACATGAAGAAAT[A/T]GAATCACTAGAGAAA | 217935 |
rs229127052 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116260560 | TAGACAGATATTCTA[C/T]AAGGTCTGAGAGACC | 217935 |
rs229132575 | in-del | -/ATC | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116223621 | TAAGTAAATAAGTAA[-/ATC]TTTTTTTTTTAAAAA | 217935 |
rs229133450 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116225833 | TTTCTAGAATTTCTA[A/G]ATCAGAACAAATGGG | 217935 |
rs229154686 | in-del | -/TC | | | intron-variant | Wdr60 | Mm_Celera | 12:116240121 | AACAAACCCAAAGAG[-/TC]CCTAGAATAGGAAAA | 217935 |
rs229187948 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116253432 | AGAAGAAGAAGTAAA[C/T]ACCCACATAGGGTAC | 217935 |
rs229215039 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116217643 | ACGGGAGACCCTAGT[A/G]TGTTTCCACATCTCT | 217935 |
rs229300076 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116258473 | GATGTAAAGAAGGAA[A/G]ATTGCATTGTGGGAG | 217935 |
rs229470290 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116232256 | CAAAATGACAACACA[A/C]TGATGAGAATAAACT | 217935 |
rs229620748 | in-del | -/GCA | | | intron-variant | Wdr60 | Mm_Celera | 12:116257518 | ATCAAGTCAGGCATG[-/GCA]GCACACACCCATATC | 217935 |
rs229636334 | in-del | -/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116230538 | GTCACTGCCTAGTTA[-/C]CAGCTCCTCTCCCTC | 217935 |
rs229680679 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116218059 | TTTAATCTCTATTCA[C/T]TTTAGCAAACAATAA | 217935 |
rs229736241 | snp | A/C | | | intron-variant, upstream-variant-2KB | Wdr60 | GRCm38.p3 | 12:116235889 | CGAAAAACAAACAAA[A/C]AGAAAAAAGAAAAAA | 217935 |
rs229813657 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116240075 | CCCAGTTCCCTACTC[G/T]TGCTTTCTGCCTGAC | 217935 |
rs229816421 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116260227 | CAGAACACTATGAAA[A/T]AAATCAAACCTCTGA | 217935 |
rs229854212 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116240811 | ACTACGGTTAAGCAT[C/T]CCTGGTCACAGCCTT | 217935 |
rs229920002 | snp | G/T | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235596 | CATACAAAGTCTGGA[G/T]TCTTACTTTCCATTC | 217935 |
rs230046998 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116254006 | TGAGCAAGCCAGTAA[A/G]CAGCACCTCTCCATG | 217935 |
rs230120889 | snp | G/T | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235021 | TACATATAATTTTAT[G/T]TATTCATTTTCATCT | 217935 |
rs230126404 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116237811 | CATGAGGAGCATATA[C/T]ATATATACACACATC | 217935 |
rs230183762 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116238531 | CCTTGCCCTACTATA[A/C]TATAACCTCTTATCT | 217935 |
rs230304372 | in-del | -/G | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116224754 | TCCCATTAGATCACA[-/G]GTGTGTACTACAAAT | 217935 |
rs230394839 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116224548 | GGCCCTTTAATACAG[C/T]TCCTCATGTTGTAGT | 217935 |
rs230445706 | snp | C/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116233137 | ACCAATTATTTATCA[C/T]GCCCCAAGAGGCTAT | 217935 |
rs230482011 | in-del | -/TG | | | intron-variant | Wdr60 | Mm_Celera | 12:116227773 | TGATGAGATGCCTTC[-/TG]TCTTTAACTGTTACT | 217935 |
rs230544701 | in-del | -/AAAAC | | | intron-variant | Wdr60 | Mm_Celera | 12:116229302 | GAAATTATAGGACTT[-/AAAAC]AAACATGGACAATCT | 217935 |
rs230544845 | snp | G/T | | | intron-variant, upstream-variant-2KB | Wdr60 | Mm_Celera | 12:116235181 | CTAATTTGCTAAGAT[G/T]TACTACACTAAGTGT | 217935 |
rs230577500 | in-del | -/GC | | | intron-variant | Wdr60 | Mm_Celera | 12:116255679 | GACATTCACACAGGA[-/GC]GCGCACACACACACA | 217935 |
rs230594946 | snp | A/T | | | intron-variant | Wdr60 | GRCm38.p3 | 12:116249364 | TGCTGCCTGTGTGTA[A/T]TACAGTGACATGTGC | 217935 |
rs230653477 | snp | G/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116226820 | ACTACATCTGCTGAC[G/T]AGTTCCTGCGGATCA | 217935 |
rs230686173 | snp | C/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116221592 | ATGGCTTCAGGAAGC[C/G]GTGGCAGGCAGCATG | 217935 |
rs230711547 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116233203 | AGTTGTGAAGCACAC[A/G]CTTTCTCCTGACTAC | 217935 |
rs230878116 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116221477 | TACTTTAGTTGACTT[A/T]GTGGCTTTGCATTTT | 217935 |
rs230948027 | snp | A/C/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Wdr60 | GRCm38.p3 | 12:116206863 | TCAACTCCTAGCCCT[A/C/G]GAGTCCCAGCCTTGG | 217935 |
rs231000584 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Wdr60 | Mm_Celera | 12:116207611 | TTCTCCCGACACCAA[A/G]TCTTCATTTCTGAAG | 217935 |
rs231015739 | snp | A/C | | | intron-variant | Wdr60 | Mm_Celera | 12:116259787 | TTCTCCAGAAGCCAG[A/C]AACCCTCTGTCACAG | 217935 |
rs231071861 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116220778 | TAGAGCCCAAGTCAT[A/T]TAACAAATTTTATAT | 217935 |
rs231106973 | snp | A/G | | | intron-variant | Wdr60 | Mm_Celera | 12:116260265 | ATGTAGAGAAGGAGA[A/G]GAGACCCACATTGAA | 217935 |
rs231179919 | snp | A/T | | | intron-variant | Wdr60 | Mm_Celera | 12:116262529 | TGGATTTTTGATATA[A/T]ACGACCTACCAAAGT | 217935 |