SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6196470 | snp | C/T | 0.5 | 0 | intron-variant | Rnf182 | Mm_Celera | 13:43620520 | ggtgacaggtgtagg[C/T]cattgtccttacttt | 328234 |
rs6197125 | snp | A/G | 0.5 | 0 | intron-variant | Rnf182 | Mm_Celera | 13:43620657 | AGTTCTTAAAGGATG[A/G]AGGCAGGNAGAGAGT | 328234 |
rs6197132 | snp | C/T | 0.5 | 0 | intron-variant | Rnf182 | Mm_Celera | 13:43620665 | AAGGATGNAGGCAGG[C/T]AGAGAGTGCTGTCGA | 328234 |
rs6197188 | snp | A/G | 0.5 | 0 | intron-variant | Rnf182 | Mm_Celera | 13:43620692 | TCGAAAGAGAAAGAG[A/G]GTAAGAAAGAAGTAC | 328234 |
rs6210076 | snp | C/T | 0.5 | 0 | intron-variant | Rnf182 | Mm_Celera | 13:43620773 | CACAGTGAGGCCCCT[C/T]CATGAGACAGTGGGA | 328234 |
rs6210604 | snp | A/C | 0.5 | 0 | intron-variant | Rnf182 | Mm_Celera | 13:43620863 | TACATGTTCTTATAG[A/C]ATATGAATTCACATA | 328234 |
rs6210700 | snp | C/T | 0.5 | 0 | intron-variant | Rnf182 | Mm_Celera | 13:43620912 | CCCTTCAGAAGTTCT[C/T]CTTTTAATTAATTAA | 328234 |
rs6278786 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Rnf182 | Mm_Celera | 13:43630134 | TAGGAGTCAGTACAC[A/T]GGAGTTTCCTTCTTT | 328234 |
rs6280233 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Rnf182 | Mm_Celera | 13:43630374 | CACTGCAGTTGACCC[A/G]AGTCTAGTGTTTGGA | 328234 |
rs6280763 | snp | A/G | 0.5 | 0 | intron-variant | Rnf182 | Mm_Celera | 13:43630450 | tgatggtttgtatat[A/G]ctcaangaagggagt | 328234 |
rs6280768 | snp | C/T | 0.5 | 0 | intron-variant | Rnf182 | Mm_Celera | 13:43630456 | tttgtatatnctcaa[C/T]gaagggagtggcact | 328234 |
rs6281376 | snp | C/T | 0.5 | 0 | intron-variant | Rnf182 | Mm_Celera | 13:43630586 | gtagaactctcagtt[C/T]ctcctncaccaggcc | 328234 |
rs6281392 | snp | A/G | 0.5 | 0 | intron-variant | Rnf182 | Mm_Celera | 13:43630592 | ctctcagttnctcct[A/G]caccaggcctgcctg | 328234 |
rs13481788 | snp | C/T | 0.493416 | 0.056998 | intron-variant | Rnf182 | Mm_Celera | 13:43632644 | ATTCAATGTTTTTTT[C/T]CCCTCTGTCTCTACA | 328234 |
rs29241092 | snp | C/G | 0.5 | 0 | intron-variant | Rnf182 | Mm_Celera | 13:43640301 | GTGAGATGGCTCAGC[C/G]GTTAAGAGCACTGAC | 328234 |
rs29547592 | snp | C/T | 0.5 | 0 | intron-variant | Rnf182 | Mm_Celera | 13:43653000 | GAGCCATTGCTCAGT[C/T]ACCTCAGCTCACTAT | 328234 |
rs29805916 | snp | C/T | 0.5 | 0 | intron-variant | Rnf182 | Mm_Celera | 13:43644707 | TACAGTGCCTGTGTG[C/T]GTGCTTGCTTAGTTT | 328234 |
rs30149064 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43662241 | GTCTTCCCCACGGCA[C/T]TGGAGACTGGAGCTG | 328234 |
rs30149065 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf182 | Mm_Celera | 13:43662219 | GAAGTGTTGGCTAGC[A/G]GCAGGTGTCTTCCCC | 328234 |
rs30149066 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43662067 | TGTAACTGGAGAGCC[A/G]CAGGAAGTGATCAGA | 328234 |
rs30149067 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Rnf182 | Mm_Celera | 13:43661968 | TAGTTGTTCAAGTGA[A/C]GTGATCTGAAACACA | 328234 |
rs30149068 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf182 | Mm_Celera | 13:43661902 | GCCCATCAGGCAATC[C/T]GGTCACTGAGTGGCA | 328234 |
rs30149069 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43661829 | GGCAAGAATAGTGAG[A/C]ACATAGGAGATTTAA | 328234 |
rs30149070 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43661782 | GAACGGCTAGAGTCA[C/T]GCTTCACAGCACAGA | 328234 |
rs30149071 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43661771 | GCAGTCTACAAGAAC[A/G]GCTAGAGTCATGCTT | 328234 |
rs30149072 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf182 | Mm_Celera | 13:43661687 | TGCAGGCACATGGGT[C/T]CTACAGGAGTCACAT | 328234 |
rs30149073 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Rnf182 | Mm_Celera | 13:43661669 | TTTGATTACTCACAG[G/T]ACTGCAGGCACATGG | 328234 |
rs30149094 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43630899 | TGGCGTGCTATTCAT[C/T]CAGCCCATTTCTTCT | 328234 |
rs30149095 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43630774 | TGACGTTAATATGTT[A/G]ACAAAGCTCTAATTT | 328234 |
rs30149096 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43630763 | CCTTTGCTTCATGAC[G/T]TTAATATGTTAACAA | 328234 |
rs30149097 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43630157 | CCTTCTTTTATTGTG[A/C]CCACTGGCCAAAGAT | 328234 |
rs30149098 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43630063 | GTGCTGGTTCTAGAA[C/T]TCAAGCTGAAGGAAC | 328234 |
rs30149099 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43630038 | GGGTTGTGTTAGATC[C/T]GTCCCCTATGTGCTG | 328234 |
rs30149100 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43629974 | AAGGTGAGCCTTGTC[A/G]GTGGCTGTGCTCCAG | 328234 |
rs30149101 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43629973 | GAAGGTGAGCCTTGT[C/T]GGTGGCTGTGCTCCA | 328234 |
rs30149102 | snp | A/C/G | 0.244898 | 0.249948 | intron-variant | Rnf182 | Mm_Celera | 13:43629431 | TAGTGCATCTATCAC[A/C/G]CGACCTGTTCATAGA | 328234 |
rs30149103 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43629415 | CCTCACAGGTTCTGG[G/T]TAGTGCATCTATCAC | 328234 |
rs30149924 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43660671 | TGTCACACACATCTG[A/G]GCTGCATTCTTCCTG | 328234 |
rs30149925 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf182 | Mm_Celera | 13:43660397 | CACAGAGATGGCTTT[C/T]CTTCTGGGCCGGGCT | 328234 |
rs30149926 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43660163 | GGGATCTGGGAGCCA[C/G]CAGCTGAAGCACCTT | 328234 |
rs30149927 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43660150 | TTATAGTTGGCGAGG[C/G]ATCTGGGAGCCAGCA | 328234 |
rs30149928 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Rnf182 | Mm_Celera | 13:43660136 | ACTTGTTGCAGGAAT[G/T]ATAGTTGGCGAGGGA | 328234 |
rs30149929 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Rnf182 | Mm_Celera | 13:43659138 | CCAAATAGGAAAGAT[G/T]CGTGTGTGTGTGTGT | 328234 |
rs30149930 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf182 | Mm_Celera | 13:43659058 | GGCAAAGTGATTTAT[C/T]TACTATGGAGTCCTT | 328234 |
rs30149931 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43658917 | CTGTTGATTAAAAGA[C/T]GAGAAAACAGGTTCC | 328234 |
rs30149932 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf182 | Mm_Celera | 13:43658479 | GCTTCTGAACTCCCG[A/C]AGGCCTGCTTTGCTT | 328234 |
rs30149933 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rnf182 | Mm_Celera | 13:43658446 | TGAGAGCACAAGTGC[A/G]GGGCACCTCACGGTC | 328234 |
rs30150234 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43629387 | CTCTGTAGGTGGTCT[C/T]ACGCACAGACCACCT | 328234 |
rs30150235 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43629316 | GCTGTCCTAGATAAA[C/T]ACTTGGTGTCCTTCT | 328234 |
rs30150236 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43629227 | GTGGAACTGTAAAGA[C/T]CTAAATACAGTCTCT | 328234 |
rs30150237 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43629185 | CCAGTCAGCTTAAGT[C/T]GTCTCTGTCTCATCA | 328234 |
rs30150238 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43628993 | CTTTTACTTGGTTGG[C/T]GTTCTCTAGTTCATC | 328234 |
rs30150239 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43628881 | TCAGTAGCCCAGTTA[A/G]CGTCAGCCATTGGTT | 328234 |
rs30150240 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43628494 | TTCTTCTAATACTTA[A/G]AACAGCACTGTCCGA | 328234 |
rs30150241 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Rnf182 | Mm_Celera | 13:43628397 | CATGGGTAGTTCTGT[C/G]TCTGACAGTGATGGA | 328234 |
rs30150242 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43625180 | TTTTGCTCATTTTAA[C/G]TGCTAAGTGCATCTG | 328234 |
rs30150243 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf182 | GRCm38.p3 | 13:43623359 | CACCTCAGCTTAGGA[C/G]GCGACACCTCAGGAG | 328234 |
rs30150884 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43658206 | GACTGTCATCCTTCA[C/T]TCTTGAGTTAGCATG | 328234 |
rs30150885 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rnf182 | Mm_Celera | 13:43658160 | GTCATAAAACACACA[C/T]CTTTGAAAGCAGAAT | 328234 |
rs30150886 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf182 | Mm_Celera | 13:43657860 | TGTGGAGCTCAATCG[A/T]TGTCTCTAAAATATC | 328234 |
rs30150887 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43657818 | CTTCAGAGCAGAACC[A/G]TGGGAATTCCACATG | 328234 |
rs30150888 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf182 | Mm_Celera | 13:43657771 | GTGCTCTCTTGTATC[C/T]GGACTTCTGTCATCT | 328234 |
rs30150889 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43657622 | TCGGACTACATGAAA[C/T]CTGTCCCTGAGATAG | 328234 |
rs30150890 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Rnf182 | Mm_Celera | 13:43657334 | CCATGGAGAGAAGGA[A/C]ACTTTTGGCACTGTC | 328234 |
rs30150891 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Rnf182 | Mm_Celera | 13:43656533 | TTTCAATTACTTGGC[A/C]CTTCCCGATGAATAG | 328234 |
rs30150892 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf182 | Mm_Celera | 13:43655329 | TTGTAATTTTCTTTC[A/G]ATCTGTGTTCCTATT | 328234 |
rs30150893 | snp | C/G | 0.32 | 0.24 | intron-variant | Rnf182 | Mm_Celera | 13:43654368 | CGTGACAGTAACTAA[C/G]GCCTCTGTGTTTGAA | 328234 |
rs30151084 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43621670 | TCACAATTTGCCCTT[G/T]TTTTTCGAATGTTCA | 328234 |
rs30151085 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf182 | Mm_Celera | 13:43621409 | ACCGGCTGAGGTCCC[A/G]TGTAGCATTAGCTCA | 328234 |
rs30151086 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf182 | Mm_Celera | 13:43619201 | ACAAATGTGGACCAA[A/G]GAACTTCTTATTGAT | 328234 |
rs30151087 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf182 | Mm_Celera | 13:43618806 | GGCTGGAGAGAAGGC[A/G]ACCCTGAGACCTCGA | 328234 |
rs30151088 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf182 | Mm_Celera | 13:43618098 | AGATTGAATGCACTG[A/G]CTGCTTAACTGTATT | 328234 |
rs30151089 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf182 | Mm_Celera | 13:43617604 | GTACTAAATACTCCT[C/T]GATGAAGGCAATGAA | 328234 |
rs30151090 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Rnf182 | Mm_Celera | 13:43616886 | GGGATACCTGATAGG[A/G]AACTGCTTAAGTTGT | 328234 |
rs30151091 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Rnf182 | Mm_Celera | 13:43616697 | ACTTGGCACAGACAT[A/C]GTTGCTATTGTTTTG | 328234 |
rs30151092 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Rnf182 | Mm_Celera | 13:43616656 | TTCTAGAGCTGTTAG[A/C]TGGACCAGTACCTTG | 328234 |
rs30151093 | snp | A/G | 0.152778 | 0.230321 | utr-variant-5-prime | Rnf182 | Mm_Celera | 13:43616015 | CCGGAGTGGCTCTCG[A/G]TCCTCCCATCGATCC | 328234 |
rs30151292 | snp | A/G | 0.132653 | 0.220748 | downstream-variant-500B | Rnf182 | Mm_Celera | 13:43671444 | TAAGACGGCTCCCTG[A/G]TCCCATGTGATTATA | 328234 |
rs30151293 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Rnf182 | Mm_Celera | 13:43671392 | GTCTAAGGTGCTTCC[A/G]AAATCTTCATACAGT | 328234 |
rs30151894 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rnf182 | Mm_Celera | 13:43654322 | GGAGGAGCTAATCTG[C/T]GTGGTGCATTACTTT | 328234 |
rs30151895 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf182 | Mm_Celera | 13:43652168 | CTTAGTCTATAGTTA[C/T]ACACCGTGGAAAATG | 328234 |
rs30151896 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rnf182 | Mm_Celera | 13:43651378 | AGAGCCCACATCTAA[C/T]GCGATTGCTCATCTG | 328234 |
rs30151897 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf182 | Mm_Celera | 13:43649911 | TGGCAGTAGATAGTT[C/T]CCATTGCCTGAATGC | 328234 |
rs30151898 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Rnf182 | Mm_Celera | 13:43649057 | ACCCTTTCTCCTCTC[C/G]CATTTTTATCTCTTG | 328234 |
rs30151899 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf182 | Mm_Celera | 13:43648329 | TGCCTAAAAGCAGCC[A/G]CTGTGTGCTAGGGAC | 328234 |
rs30151900 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf182 | Mm_Celera | 13:43647836 | CCTTCAAGTCTGGCT[A/G]CCAGGATCCACCAGA | 328234 |
rs30151901 | snp | C/G | 0.5 | 0 | intron-variant | Rnf182 | Mm_Celera | 13:43642153 | TTGGTGGTTTCTCTC[C/G]GTTTTCTATTTTCTA | 328234 |
rs30151902 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf182 | Mm_Celera | 13:43638993 | AGGGGCAGTTTCCCA[A/C]TCTGTCTCCAGTCTA | 328234 |
rs30151903 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf182 | Mm_Celera | 13:43638846 | CTTTTCAACAACTAC[C/T]AACCACAGCCATGCT | 328234 |
rs30151934 | snp | C/G | 0.152778 | 0.230321 | utr-variant-5-prime | Rnf182 | Mm_Celera | 13:43616011 | GCCGCCGGAGTGGCT[C/G]TCGATCCTCCCATCG | 328234 |
rs30151935 | snp | C/G | 0.18 | 0.24 | utr-variant-5-prime | Rnf182 | Mm_Celera | 13:43615882 | CGGCCGGCCCCGGCA[C/G]TGGCGGTTGCCATGG | 328234 |
rs30151936 | snp | C/T | 0.142012 | 0.225474 | upstream-variant-2KB, utr-variant-5-prime | Rnf182 | Mm_Celera | 13:43615288 | TGTGTGTAAAAGTTG[C/T]GGTTTAACATCTCGT | 328234 |
rs30151937 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB, utr-variant-5-prime | Rnf182 | Mm_Celera | 13:43615200 | CTCTGTCACTTGGTG[C/T]CCATGGTGGATGCTT | 328234 |
rs30151938 | snp | G/T | 0.142012 | 0.225474 | upstream-variant-2KB, utr-variant-5-prime | Rnf182 | Mm_Celera | 13:43615186 | CAGCTAGACGGTGGC[G/T]CTGTCACTTGGTGCC | 328234 |
rs30151939 | snp | A/G | 0.152778 | 0.230321 | upstream-variant-2KB | Rnf182 | Mm_Celera | 13:43614373 | TGAGTTTTGATACAT[A/G]TCTTCAAATGACTTA | 328234 |
rs30151940 | snp | A/G | 0.152778 | 0.230321 | upstream-variant-2KB | Rnf182 | Mm_Celera | 13:43613353 | GGTTTTACCAAGTAC[A/G]GTGCTAGCCCTAGCC | 328234 |
rs30151941 | snp | A/C | 0.142012 | 0.225474 | upstream-variant-2KB | Rnf182 | Mm_Celera | 13:43613177 | CTGGTCCTTTCGATC[A/C]TCACTCTTGTTAGGG | 328234 |
rs30151942 | snp | C/T | 0.142012 | 0.225474 | upstream-variant-2KB | Rnf182 | Mm_Celera | 13:43613172 | TAGCGCTGGTCCTTT[C/T]GATCCTCACTCTTGT | 328234 |
rs30152154 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Rnf182 | Mm_Celera | 13:43671122 | TTTTTCCAAGTTGAG[C/T]AGATGATGAAATAAG | 328234 |
rs30152155 | snp | C/T | 0.244898 | 0.249948 | downstream-variant-500B | Rnf182 | Mm_Celera | 13:43671017 | AATGTGCACTTTCAT[C/T]AAGCCAATGCTTTTT | 328234 |