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 |