SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4223067 | snp | A/C | 0.244898 | 0.249948 | utr-variant-3-prime | Wdr5 | GRCm38.p3 | 2:27536087 | GGGACAAGCCTTGGC[A/C]AAGGCAGAGTAGAGC | 140858 |
rs4223068 | snp | A/C | 0.244898 | 0.249948 | utr-variant-3-prime | Wdr5 | GRCm38.p3 | 2:27536063 | GTAGAGCAGCTACTG[A/C]CCTGGGTGATGTGGC | 140858 |
rs4223069 | snp | G/T | 0.244898 | 0.249948 | utr-variant-3-prime | Wdr5 | GRCm38.p3 | 2:27536056 | AGCTACTGCCCTGGG[G/T]GATGTGGCTTCAATA | 140858 |
rs4223070 | snp | A/G | 0.30839 | 0.243086 | utr-variant-3-prime | Wdr5 | GRCm38.p3 | 2:27535907 | TGCAGTCTGCTCCAC[A/G]GTAGGTCACCCTGGG | 140858 |
rs27200218 | snp | A/C | 0.132653 | 0.220748 | downstream-variant-500B | Wdr5 | Mm_Celera | 2:27536665 | GGATTTCTTTAGCAG[A/C]ACAGGCAGTGGAGGA | 140858 |
rs27200219 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Wdr5 | Mm_Celera | 2:27535856 | AGTGGCCAAGCTCAG[A/G]ACTACACAGCATTTT | 140858 |
rs27200220 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime | Wdr5 | Mm_Celera | 2:27535428 | TACACACACTGTAAT[A/G]AAAGGTGGGTATGGA | 140858 |
rs27200221 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Wdr5 | Mm_Celera | 2:27535295 | AGTTTCTGGAAACAC[A/G]GAAAGGTTGTAAGTT | 140858 |
rs27200222 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Wdr5 | Mm_Celera | 2:27535050 | TCTGTCTCTGCCTGG[A/G]GAAGTTCCTGGTCTG | 140858 |
rs27200223 | snp | A/C | 0.132653 | 0.220748 | utr-variant-3-prime | Wdr5 | Mm_Celera | 2:27534964 | CCTGGTGCACCTCCT[A/C]TCTGAAGATGTCGGC | 140858 |
rs27200224 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Wdr5 | Mm_Celera | 2:27534727 | GGGACTGCTTGTCCT[A/G]GAGTGGCTCCCTGAC | 140858 |
rs27200225 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Wdr5 | Mm_Celera | 2:27534713 | GTGAGGCATGTGCTG[C/G]GACTGCTTGTCCTAG | 140858 |
rs27200226 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27534593 | CCTGCTGGGTACCCA[C/T]CAAGTGCCTTGTGCC | 140858 |
rs27200227 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr5 | Mm_Celera | 2:27534537 | GTAGGGGGCAAGTGG[A/G]CATAGTCAGTCCTGA | 140858 |
rs27200228 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Wdr5 | Mm_Celera | 2:27534479 | AGTATCCCTGCCCAG[A/G]TGTATGGTTACCTTG | 140858 |
rs27200229 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27534373 | AAAAGCAGTTGTCTT[C/T]AGCTGGGAGTGGCTT | 140858 |
rs27200230 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr5 | Mm_Celera | 2:27534341 | CAACCCTAAGGAGTG[A/G]AGAGCTCGTTTTCTG | 140858 |
rs27200231 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27534196 | CTGTAGGCTCAGCCT[C/T]TTTCAGGGATGCTGG | 140858 |
rs27200232 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27533859 | AGGGTCACACAGGTG[A/G]GTAGTTATTGCAGAT | 140858 |
rs27200233 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Wdr5 | Mm_Celera | 2:27533743 | TGCCTGTCCTCACTG[C/G]CTGCTTGTTCTTTCG | 140858 |
rs27200234 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27533607 | CTGGATAGATCCAGT[A/G]ACTGAGGGTGCCGTG | 140858 |
rs27200235 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr5 | Mm_Celera | 2:27533581 | GTTGAAGATCTAAGA[A/G]CAGGTGGTGACTGGA | 140858 |
rs27200236 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr5 | Mm_Celera | 2:27533562 | TGTGTTGCACTTGGA[C/T]ATGGTTGAAGATCTA | 140858 |
rs27200237 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr5 | Mm_Celera | 2:27533325 | GCTAACAATGCACAC[C/T]TACCTTTTCAGTGCC | 140858 |
rs27200238 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27533283 | CCCAGAATTTGGAAT[C/G]CTCTGGAATGAAAGC | 140858 |
rs27200239 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr5 | Mm_Celera | 2:27533138 | CTTGGGCATCTTCTT[C/T]TGATGAGCAAGTATG | 140858 |
rs27200240 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27532911 | TCTTTCCTGACTCAC[A/G]GTTGTTAGGATACGG | 140858 |
rs27200241 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr5 | Mm_Celera | 2:27532863 | TGCTTTTGTGTGTCA[C/T]GGAGTGGCTGGGCTT | 140858 |
rs27200242 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Wdr5 | Mm_Celera | 2:27532813 | AATCTGTTTCTTCAG[C/T]CTGTTTCTGAGCTGA | 140858 |
rs27200243 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Wdr5 | Mm_Celera | 2:27532716 | TCTCTTCCTGTGGCA[C/T]CTGTACTGGGTGTTT | 140858 |
rs27200244 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27532062 | ACCTGGCCAAGTTAG[C/T]TCTTGAGAGCTGCCT | 140858 |
rs27200245 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Wdr5 | Mm_Celera | 2:27531963 | TCTGAGCATCTTCAC[G/T]CAGCATAATCTCACT | 140858 |
rs27200246 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27531920 | TGAGAAGGATTTGAC[A/G]CCTAGTTGTTCCTGC | 140858 |
rs27200247 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr5 | Mm_Celera | 2:27531889 | AAAGGACTGTCCACT[C/T]TAGCTAGTTTTAGTA | 140858 |
rs27200248 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27531805 | TGTTTCTTCTCCCAG[C/T]TGTCCAGTTGAACTC | 140858 |
rs27200249 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdr5 | Mm_Celera | 2:27531518 | GGTGATGGCATGTCA[A/G]AGCTCTCTGGTGTCC | 140858 |
rs27200250 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Wdr5 | Mm_Celera | 2:27531334 | AGAAAGGAGAACTTG[A/C]TTGGCTGAAGAATGG | 140858 |
rs27200251 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27531172 | AAGGATATGACTTTG[G/T]TGTGCTCTGGAAAGC | 140858 |
rs27200252 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Wdr5 | Mm_Celera | 2:27531073 | CTTCCTTGGCTGGCC[A/G]AGCAGGCCCACCTCA | 140858 |
rs27200253 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Wdr5 | Mm_Celera | 2:27531029 | AGGGTACACCAGCCT[C/T]TTGTATGCACACTTT | 140858 |
rs27200254 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27530882 | GCCTGGAAAGGCGCA[C/T]AGGTGTTGCTCCATG | 140858 |
rs27200255 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Wdr5 | Mm_Celera | 2:27530674 | AGGTTTAGACATTAA[C/G]GTTTAGACATTCTTT | 140858 |
rs27200256 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Wdr5 | Mm_Celera | 2:27530193 | TGTGTTTCCCAGTAT[A/G]CACATGTCCATGTGC | 140858 |
rs27200257 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27529936 | AGTTGTCCTAGGGAA[A/C]AGTGAAATTCTGTTT | 140858 |
rs27200258 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27529883 | CATGCAGCTCCAAGA[A/G]GGAATGCTAGAGTTG | 140858 |
rs27200259 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Wdr5 | Mm_Celera | 2:27529299 | CAACTGTCTGGTGCT[A/G]AGTATGTTACTCAGC | 140858 |
rs27200260 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27529218 | TACTGATTTTTCAGA[A/G]CAGTCACAGATGTCA | 140858 |
rs27200261 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Wdr5 | Mm_Celera | 2:27529183 | TAAGCTTTTCTTGCT[C/G]TGTGTCCACTCTTGG | 140858 |
rs27200262 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Wdr5 | Mm_Celera | 2:27528918 | AGAATCAGGAGCTCA[G/T]CCTCTATGGCAGCTT | 140858 |
rs27200263 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Wdr5 | Mm_Celera | 2:27528866 | GGGAAACGAGTGTAG[C/T]GCTCTTGGCCTGCCA | 140858 |
rs27200264 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27528824 | TAGATAGGCATTGTG[C/G]TAAGTTGCTACCTCC | 140858 |
rs27200265 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr5 | Mm_Celera | 2:27528755 | CTGTTACTTGCTAGG[C/T]TGGAGTTCAGAACCT | 140858 |
rs27200266 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27528474 | CTTCCTGACTACGAA[A/C]GTTTACCAGAACTTG | 140858 |
rs27200267 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr5 | Mm_Celera | 2:27528445 | CCTTATTCTGCAGGA[C/T]TTGTGGCACCTTTCT | 140858 |
rs27216768 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27528255 | TGACTTTCTCATACC[C/T]TATCTTCTTGCTTGA | 140858 |
rs27216769 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr5 | Mm_Celera | 2:27527414 | GTCATTTTGTAACAA[C/T]TTTGTCCTCCTAACA | 140858 |
rs27216770 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr5 | Mm_Celera | 2:27527226 | GCAGATTTGGAATCT[A/G]TTCTGGCCTGCCGCT | 140858 |
rs27216771 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Wdr5 | Mm_Celera | 2:27527184 | GCTGGACAGCGCAGG[G/T]CCTGGGTTCCAGAGA | 140858 |
rs27216772 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr5 | Mm_Celera | 2:27527085 | ACTGTTAACAGAGAT[C/T]TTTCCCCATCATCTA | 140858 |
rs27216773 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr5 | Mm_Celera | 2:27527042 | TGCCCTCTCCTATTA[C/T]AGCATTCCTACATAT | 140858 |
rs27216774 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27526949 | AATGCATTCTCCACA[C/T]AGGCTCAGTGACTGA | 140858 |
rs27216775 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr5 | Mm_Celera | 2:27526926 | AAACACTAAGGAACT[A/G]AAATCCAAATGCATT | 140858 |
rs27216776 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr5 | Mm_Celera | 2:27526488 | AAGACTCTAATAGCC[C/T]TCGTCCCCTCTGTAT | 140858 |
rs27216777 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27526446 | TAGCAGTAGAGAGGT[C/G]GGTGCCCTGAGTTCA | 140858 |
rs27216778 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Wdr5 | Mm_Celera | 2:27526321 | CATAGGCAGAGCGGC[A/C]CAAGAGACCCCAGGT | 140858 |
rs27216779 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27526139 | CAGTTGGCAACATTA[C/T]TTGTTTCCTGGCCAC | 140858 |
rs27216780 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27526113 | TGCTGTTTGACTGCA[C/T]AGGGCCGGGCCAGTT | 140858 |
rs27216781 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr5 | Mm_Celera | 2:27526101 | CAGCTGGAGCTCTGC[C/T]GTTTGACTGCACAGG | 140858 |
rs27216782 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27526077 | GAGTTGAGCCTTGTT[A/G]CAGTTGCTCAGCTGG | 140858 |
rs27216783 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdr5 | Mm_Celera | 2:27526019 | AAAACCTAGACAGAA[C/T]GGAGAGAAGGTGAAC | 140858 |
rs27216784 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr5 | Mm_Celera | 2:27525995 | CACTGCCACCAAAAG[A/G]CAGAAAGGAAAACCT | 140858 |
rs27216785 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr5 | Mm_Celera | 2:27525935 | GACAGGGAAGAGTGG[C/T]CTAGAGTGAACCAAA | 140858 |
rs27216786 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr5 | Mm_Celera | 2:27525786 | GTGATGGGCTGGTTA[C/T]GTATCCTCACTCAGG | 140858 |
rs27216787 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Wdr5 | Mm_Celera | 2:27525479 | CCATGAGCTCTGGGC[A/T]GGTGAACCACCAGAT | 140858 |
rs27216788 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdr5 | Mm_Celera | 2:27525259 | GGGCCTGTGCCTCCT[C/T]ATCCTCCTGAGGCCT | 140858 |
rs27216789 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr5 | Mm_Celera | 2:27525185 | GAGTCTTCATGTAGT[C/G]GGTGACCTGTTGTTT | 140858 |
rs27216790 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27524975 | TGGGCAAGATGCCCT[C/T]GAGATTTAGATAAAC | 140858 |
rs27216791 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27524803 | ATCTAGATATCAGAA[A/G]CTCAGGCTGATGAAT | 140858 |
rs27216792 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27524737 | ACAGTTTATGGTGGC[C/T]TGGCTCTCATTGCTG | 140858 |
rs27216793 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27523871 | AGCCGTTCACTGTGT[C/T]TCATCCCCAGTAGGG | 140858 |
rs27216794 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Wdr5 | Mm_Celera | 2:27520519 | ACAAGAAGCTTGTAT[C/T]TGGAGATTCAGCCCC | 140858 |
rs27216795 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Wdr5 | Mm_Celera | 2:27520504 | TAGGTCTTCAAATGT[A/G]CAAGAAGCTTGTATT | 140858 |
rs27216796 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr5 | Mm_Celera | 2:27520164 | CTAAGAAGTTTGGTA[A/G]AGCTGAAAGTACTGG | 140858 |
rs27216797 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27520071 | CCTGCCTAAGAATCG[C/G]GCTTGCTCTACCATA | 140858 |
rs27216798 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr5 | GRCm38.p3 | 2:27519639 | GTGAAGGGTGTACTT[C/T]TGTGTGTCCATACTT | 140858 |
rs27216799 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr5 | Mm_Celera | 2:27519487 | GTCCTTTGGAGAGGC[A/G]TCTGAACTTTGTTGG | 140858 |
rs27216800 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Wdr5 | Mm_Celera | 2:27519445 | CCCAATGGGGAATGG[C/T]TGGCAAGTTCATGTG | 140858 |
rs27216801 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27519187 | CTTTCAAGAGAGGTG[C/G]TAGGCTCACACTGGC | 140858 |
rs27216802 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27519134 | CAAAAAAAATTACAA[A/G]TTCTTGGTGTGCTAA | 140858 |
rs27216803 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdr5 | Mm_Celera | 2:27518891 | ATTTCTGAGCACACA[A/G]CAGTGGTCACACAGA | 140858 |
rs27216804 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr5 | Mm_Celera | 2:27518870 | CCAGTGAGGTATGCT[A/G]CCAGTATTTCTGAGC | 140858 |
rs27216805 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27518800 | AGAGCAAGGTATGTC[C/T]CACAGGCTGGAGAGA | 140858 |
rs27216806 | snp | C/T | 0.124444 | 0.216185 | utr-variant-5-prime | Wdr5 | Mm_Celera | 2:27518633 | TTTGTTTATAGGCCC[C/T]TTACTATAGAGTTCA | 140858 |
rs27216807 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27517722 | CAGAGTGTCTGAAGC[A/G]TCAGCCCTGGGATAG | 140858 |
rs27216808 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr5 | Mm_Celera | 2:27517682 | ATACACCTGTCTGCT[A/G]CAGTGGGAAGCCTAG | 140858 |
rs27216809 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27517668 | ACTCACATCCCTGTA[C/T]ACACCTGTCTGCTAC | 140858 |
rs27216810 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr5 | Mm_Celera | 2:27517626 | AGAAAGCCTTTTAAA[C/T]ACTGTGTCAAGGGCT | 140858 |
rs27216811 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wdr5 | Mm_Celera | 2:27517463 | ATTGTTAAAGGCATG[G/T]TGCAGTTTATGAGGT | 140858 |
rs27216812 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Wdr5 | Mm_Celera | 2:27517402 | TCTTGGAGCGCTTTC[G/T]GTAGTACTTTGTGCA | 140858 |
rs27216813 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr5 | Mm_Celera | 2:27517326 | GCAGCTTATCTGCTG[C/T]TGTTTGTGCTGCTCC | 140858 |