SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs36241420 | snp | A/G | 0.5 | 0 | intron-variant | Dcaf4 | Mm_Celera | 12:83535761 | AAACTGAATGCGGAA[A/G]GTGTAAAAAGTGTTA | 73828 |
rs36267260 | snp | A/C | 0.5 | 0 | intron-variant | Dcaf4 | Mm_Celera | 12:83532721 | ATACCTCCATTATAT[A/C]ATTTGTAGGAAGTGG | 73828 |
rs36283503 | snp | C/G | 0.32 | 0.24 | synonymous-codon | Dcaf4 | Mm_Celera | 12:83537963 | GTCTCGGAGGGTCCT[C/G]TTGACCAATGTGGTG | 73828 |
rs36286319 | snp | C/G | 0.375 | 0.216506 | intron-variant | Dcaf4 | Mm_Celera | 12:83532592 | CCTTTAATCCCATCC[C/G]GTGAAATAAACCTGG | 73828 |
rs36310973 | snp | A/C | 0.336735 | 0.234472 | downstream-variant-500B | Dcaf4 | Mm_Celera | 12:83542215 | ACAGCTTTGTTTCTG[A/C]GGACTCAGGACCAGG | 73828 |
rs36393630 | snp | A/G | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Dcaf4 | Mm_Celera | 12:83531468 | TTTGTGATGTCCACT[A/G]GTTAGGTCTAGTTAG | 73828 |
rs36413057 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83535623 | TGGGCATGTTATACC[A/G]CAGCCTTACCAGACT | 73828 |
rs36429592 | snp | A/C | 0.32 | 0.24 | intron-variant | Dcaf4 | Mm_Celera | 12:83534793 | CAGCCATTTTCTAGG[A/C]AAGCATCTTACAGTT | 73828 |
rs36443540 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Dcaf4 | Mm_Celera | 12:83539597 | CTCCATAAGCTTAGC[C/T]TTGTCTTGATAGAAG | 73828 |
rs36471423 | snp | A/G | 0.375 | 0.216506 | intron-variant, utr-variant-5-prime | Dcaf4 | Mm_Celera | 12:83531053 | GTTTAATAAAGACAC[A/G]GAGACATCTATATAA | 73828 |
rs36510582 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Dcaf4 | Mm_Celera | 12:83540400 | GTCCAGAAGCCTTGT[G/T]AGCTAATGTCCCTAC | 73828 |
rs36538923 | snp | C/T | 0.5 | 0 | intron-variant | Dcaf4 | Mm_Celera | 12:83528564 | AATTTAAGCCTTCTG[C/T]TGCTGTAGCCAATGA | 73828 |
rs36538977 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Dcaf4 | Mm_Celera | 12:83539523 | AAGATAGCAGGGTGC[A/G]GGTCACACAGATGTA | 73828 |
rs36539398 | snp | C/G | 0.375 | 0.216506 | intron-variant | Dcaf4 | Mm_Celera | 12:83540150 | AAGCTCACTTAACAT[C/G]AGCAGCCATTCTGCT | 73828 |
rs36570990 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon, utr-variant-5-prime | Dcaf4 | Mm_Celera | 12:83532363 | TGCTCTGGCAAGTGA[C/T]CGGTTTAACTTCATC | 73828 |
rs36595502 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83532032 | GAGGAAGGGCTACCC[A/G]GTCTGTCAGTTGTCC | 73828 |
rs36625927 | snp | C/T | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Dcaf4 | Mm_Celera | 12:83531100 | CTTTTGCTGGGAATG[C/T]CTCTCAGCTAGCCTC | 73828 |
rs36626843 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83532947 | AGCAGTGATCTGCTG[G/T]CAAGATGAGAGGCTA | 73828 |
rs36686271 | snp | C/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Dcaf4 | Mm_Celera | 12:83530256 | GTGCTATCAGAGTTT[C/G]CCTGACATGGAAATG | 73828 |
rs36709410 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83535735 | GTGACATTATGTTCC[C/T]GAAGAGACGGAAACT | 73828 |
rs36738872 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB | Dcaf4 | Mm_Celera | 12:83519031 | TTGGGGTCATACATA[A/G]CCTTTACTCTTCAGG | 73828 |
rs36746681 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Dcaf4 | Mm_Celera | 12:83540034 | GCCCTCTATCATTAG[A/G]TCAGTGGCAGGCAGC | 73828 |
rs36748449 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83528182 | GGAGCGGCAGCCCTT[A/G]GAGAGAAAGGCCAGC | 73828 |
rs36755190 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83534941 | GAATGGGTTTAGTAC[G/T]CAGCCAGGTGCTTGC | 73828 |
rs36772761 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83540423 | GTCCCTACAGAAAGT[G/T]CTCACCCGTTCCATT | 73828 |
rs36779190 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83533757 | CTTTGTTGGCGTGTA[C/G]TCACGGAGCGGGAGT | 73828 |
rs36801637 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Dcaf4 | Mm_Celera | 12:83539976 | CTTAACCAGCAGAGG[C/G]AGAAAGTGGTAAATA | 73828 |
rs36803941 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Dcaf4 | Mm_Celera | 12:83522681 | GAACTCTTGGTGAGC[C/T]ATCTGCATTTTCTCA | 73828 |
rs36829989 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf4 | Mm_Celera | 12:83538921 | CCTAAGGGGACCGTG[A/G]ATCTACCTCCAGGCA | 73828 |
rs36834708 | snp | G/T | 0.165289 | 0.235211 | upstream-variant-2KB, intron-variant | Dcaf4 | GRCm38.p3 | 12:83524667 | GACTCCAGCCCTGTA[G/T]CGAAACAAAATAGGA | 73828 |
rs36847851 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf4 | Mm_Celera | 12:83539715 | GATCATGTCACCCCT[C/T]CGGCTGCATACCTGG | 73828 |
rs36848380 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83536282 | TTGATTAAGCTCCCA[C/T]GTGTGGTATGTATGC | 73828 |
rs36858442 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83527927 | TTGGAGCCTGGAGCA[C/T]ACAGCAAGTCTCACT | 73828 |
rs36861798 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Dcaf4 | Mm_Celera | 12:83529737 | GTACGGACCTCAGTG[A/G]CTGACCAGGAATGTC | 73828 |
rs36870095 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Dcaf4 | Mm_Celera | 12:83538551 | CTCGTGAGTAGCCTG[A/G]CATTCCATCCTTGGA | 73828 |
rs36879521 | snp | A/G | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Dcaf4 | Mm_Celera | 12:83531542 | TGAGAAGAGACCCAC[A/G]TGCAGAGAGGCCGTG | 73828 |
rs36892318 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Dcaf4 | Mm_Celera | 12:83539655 | GATGGACACAAGGCT[C/T]ACAAGTCAGAGGCAT | 73828 |
rs36921475 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83538581 | AGCACACAACAAAAC[A/C]GTGCAGCTCTAACAC | 73828 |
rs36963078 | snp | C/G | 0.297521 | 0.245442 | intron-variant | Dcaf4 | Mm_Celera | 12:83537865 | GAACTCCACAGACCT[C/G]AAGACCCCATCCAGC | 73828 |
rs36997479 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Dcaf4 | Mm_Celera | 12:83537940 | CGTTTCTTGTCTCCA[C/T]CAGGTTTGTCTCGGA | 73828 |
rs37044770 | snp | C/G | 0.244898 | 0.249948 | synonymous-codon | Dcaf4 | Mm_Celera | 12:83541609 | GCTCCCTTCTGTTTC[C/G]AATGAGGACATTTTA | 73828 |
rs37057494 | snp | A/G | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Dcaf4 | Mm_Celera | 12:83531728 | TTCCTCTACATGCAC[A/G]TGAGATAGACTAGTG | 73828 |
rs37105864 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Dcaf4 | Mm_Celera | 12:83540055 | GGCAGGCAGCACCCT[A/C]GAGACAGACAGGTAG | 73828 |
rs37161195 | snp | C/T | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Dcaf4 | Mm_Celera | 12:83531832 | TCTGTCTGCTTGACC[C/T]GGAGAGGAAGCTGTC | 73828 |
rs37191876 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83533783 | GGAGTAAGTCGGGTC[C/T]CTGCCTTATTCCCTG | 73828 |
rs37237903 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf4 | Mm_Celera | 12:83527874 | CTCTGTCCCATCTTA[C/T]TCTGTCCTGTGAAGA | 73828 |
rs37288890 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf4 | Mm_Celera | 12:83540208 | ATTAAGGGTACCCAA[C/T]GAACTTGGATCCTGG | 73828 |
rs37292163 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Dcaf4 | Mm_Celera | 12:83537380 | CTGAGAGTTCTGAGC[A/C]ACAGAATTCCAGCAG | 73828 |
rs37337944 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83527269 | TTTCTTCAACACATA[A/T]GCGGTTTCCACATGT | 73828 |
rs37360501 | snp | C/T | 0.297521 | 0.245442 | downstream-variant-500B | Dcaf4 | Mm_Celera | 12:83542412 | AGCGGCAGCTTTTGG[C/T]TTGCCAGTTCCACCC | 73828 |
rs37399130 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf4 | Mm_Celera | 12:83540268 | GAGCAGCAGCTATCT[A/G]GCCACTACACCCTGA | 73828 |
rs37593959 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf4 | Mm_Celera | 12:83539000 | TCTATCCTCTTACTA[A/G]AACTCAGCTTCCTAC | 73828 |
rs37644089 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83536410 | CTCCAGGCAGAGACG[A/G]CCCAAAGTACAGCTA | 73828 |
rs37710596 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf4 | Mm_Celera | 12:83538868 | CACCAGAGCCATAGC[A/G]GATACAGGGAGACAT | 73828 |
rs37742696 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Dcaf4 | Mm_Celera | 12:83539570 | GGGGCAATCCTGGGA[A/G]CTCCTTTGCTGCTCC | 73828 |
rs37773570 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83534817 | TACAGTTGTTCTCCA[C/T]GAGCAGCAGTCAGCC | 73828 |
rs37782587 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf4 | Mm_Celera | 12:83539490 | TGGAAAGGTAGGGAA[C/T]GCTCACCTCGGGCCT | 73828 |
rs37789168 | snp | A/G | 0.444444 | 0.157135 | missense, upstream-variant-2KB, utr-variant-5-prime | Dcaf4 | Mm_Celera | 12:83529172 | TGTGTCAACAGGTAC[A/G]CCACAGGGGCATCTC | 73828 |
rs37825029 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf4 | Mm_Celera | 12:83540085 | GGGACTGAGTTGGAC[A/G]TTGGGCCTCTTTGAA | 73828 |
rs37901386 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Dcaf4 | Mm_Celera | 12:83540652 | GAGTCCCAGAGTCAC[C/T]GAGTGGTCATTTGGG | 73828 |
rs37958830 | snp | A/C/G | 0.444444 | 0.157135 | missense, upstream-variant-2KB, utr-variant-5-prime | Dcaf4 | Mm_Celera | 12:83529211 | CAAGATTCTGGCCAC[A/C/G]ATGATGCTGAGTCCC | 73828 |
rs38076326 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83541288 | TAGCCCTGAGAGGTC[A/C/G]TGAGAAGCAATGTCC | 73828 |
rs38082779 | snp | C/G | 0.32 | 0.24 | intron-variant | Dcaf4 | Mm_Celera | 12:83540238 | GCCTTCTAACATACT[C/G]ATGATCTACCAAAGG | 73828 |
rs38109649 | snp | C/T | 0.18 | 0.24 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Dcaf4 | Mm_Celera | 12:83526048 | TAAAGGCGTGGGTGG[C/T]AGCCTTAGCAGTGAC | 73828 |
rs38210328 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Dcaf4 | Mm_Celera | 12:83537344 | TTACCACTGAACAGA[A/T]AAGGAGACTGAAGTC | 73828 |
rs38342021 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf4 | Mm_Celera | 12:83538760 | TTGGGCAGGAGCAGA[A/G]CTGGCCACTTAGCCC | 73828 |
rs38375246 | snp | C/T | 0.5 | 0 | intron-variant | Dcaf4 | Mm_Celera | 12:83535023 | GGGAAAAGTCTACAC[C/T]TGGGTCCACAACAGG | 73828 |
rs38468929 | snp | A/C | 0.260355 | 0.249785 | upstream-variant-2KB | Dcaf4 | Mm_Celera | 12:83519858 | TGACCTATTTGAACC[A/C]ATTCTGCTCTCACTA | 73828 |
rs38543329 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-5-prime | Dcaf4 | Mm_Celera | 12:83531374 | CCAGCAGCTCAGTGT[A/G]GAGTTGTACTTGCTT | 73828 |
rs38811577 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Dcaf4 | Mm_Celera | 12:83537824 | GTACAGGTGAGCCAT[A/G]GCCATCTCCCTGGGT | 73828 |
rs38988595 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf4 | Mm_Celera | 12:83539670 | CACAAGTCAGAGGCA[C/T]CCGTCTTCCTAGTAT | 73828 |
rs39943004 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Dcaf4 | Mm_Celera | 12:83541648 | GCTTGCTGTATGCAA[A/G]TGGAGTCCTTCAGCC | 73828 |
rs46609551 | snp | A/G | | | intron-variant, utr-variant-5-prime | Dcaf4 | Mm_Celera | 12:83531208 | CATCTGCCTGTATCT[A/G]CCTGCAGGCTCAGCT | 73828 |
rs46686201 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dcaf4 | Mm_Celera | 12:83530492 | TCAAATTTCATTGAT[C/T]GGATTTCTGTTCATT | 73828 |
rs49480496 | snp | C/T | | | intron-variant, utr-variant-5-prime | Dcaf4 | Mm_Celera | 12:83530938 | TGTCTTTGGATGTTC[C/T]TTCTGTAGTTCACAC | 73828 |
rs50432481 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dcaf4 | Mm_Celera | 12:83529970 | AGTTGAATTCTTTTT[C/T]CTAAAGAACTTCCAG | 73828 |
rs52359995 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dcaf4 | Mm_Celera | 12:83530726 | GTTTATGCCCACATG[A/G]CTGCCTTCACTGAAT | 73828 |
rs108058240 | snp | G/T | | | intron-variant | Dcaf4 | Mm_Celera | 12:83526913 | TTTTTTTTTTTTTTT[G/T]GGTTTTTTGAGACAG | 73828 |
rs211701402 | snp | C/T | | | upstream-variant-2KB | Dcaf4 | Mm_Celera | 12:83518925 | TGTGTGGCTTCCTTT[C/T]ACCTCTGGATATTAT | 73828 |
rs211703530 | in-del | -/T | | | intron-variant | Dcaf4 | Mm_Celera | 12:83534543 | CCCTACAAGTCCGTC[-/T]TTTTTTCTGTCCCTC | 73828 |
rs211856956 | snp | A/T | | | intron-variant | Dcaf4 | Mm_Celera | 12:83526366 | CTCGAAAGCTTGACG[A/T]GTTGCCTGCCATCAG | 73828 |
rs211925701 | snp | A/C | | | intron-variant | Dcaf4 | Mm_Celera | 12:83539213 | ATCAGCCACCCTTCT[A/C]ACTCCACTAAGACCA | 73828 |
rs212005849 | in-del | -/TA | | | intron-variant, upstream-variant-2KB | Dcaf4 | Mm_Celera | 12:83529435 | TTCTTTTTTTTTTTT[-/TA]AAGATTTATTTATTT | 73828 |
rs212074467 | in-del | -/TTTTTGGGTT | | | intron-variant | Dcaf4 | Mm_Celera | 12:83526673 | TGAACTCCAAGTTGG[-/TTTTTGGGTT]TTTTTTTGGTGTGTA | 73828 |
rs212143827 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Dcaf4 | Mm_Celera | 12:83525685 | GAGGTGGACATCTGG[-/A]GGGGGAGGGGGGTGT | 73828 |
rs212264713 | in-del | -/TCTCAA | | | intron-variant | Dcaf4 | Mm_Celera | 12:83541058 | CCCCAGAGCAGTGGT[-/TCTCAA]TCTTCCTACCACTGC | 73828 |
rs212357519 | snp | A/G | | | intron-variant | Dcaf4 | Mm_Celera | 12:83532078 | AGCCCTGCTGTGGAA[A/G]TGGGTGTGGGAAAGG | 73828 |
rs212402472 | snp | C/T | | | intron-variant, utr-variant-5-prime | Dcaf4 | Mm_Celera | 12:83531802 | TCCTGCATCTCCTTC[C/T]CAAGAGGGCAGAAGT | 73828 |
rs212429167 | snp | C/T | | | intron-variant | Dcaf4 | Mm_Celera | 12:83537938 | TCCGTTTCTTGTCTC[C/T]ATCAGGTTTGTCTCG | 73828 |
rs212467618 | snp | A/G | | | intron-variant | Dcaf4 | Mm_Celera | 12:83538446 | GGAACTGCCTCCCAA[A/G]CTCCTTAGCCAGTTG | 73828 |
rs212484070 | snp | C/T | | | intron-variant | Dcaf4 | Mm_Celera | 12:83541352 | TCTCTGTGTTATTTT[C/T]CCTCTTTCTTAGTGG | 73828 |
rs212629660 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Dcaf4 | Mm_Celera | 12:83525763 | AGAATTTGTGCCGGG[C/T]GTGGTAGCGCACACC | 73828 |
rs212763342 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dcaf4 | Mm_Celera | 12:83529570 | GAACTCAGGACCCTC[A/G]GAAGAGCAGTCAGTG | 73828 |
rs212840112 | snp | A/G/T | | | intron-variant | Dcaf4 | GRCm38.p3 | 12:83535516 | ACTTGTTTCACACGT[A/G/T]TTCATGAGTTCAGTC | 73828 |
rs212874553 | snp | C/G | | | intron-variant, upstream-variant-2KB | Dcaf4 | Mm_Celera | 12:83528936 | CTGGGTTTATAGGTA[C/G]ACTGGTTTGATTCCC | 73828 |
rs212876580 | snp | A/G | | | intron-variant | Dcaf4 | Mm_Celera | 12:83535839 | AAGGATACTGATGGC[A/G]TCCTTCTCCCAGAGG | 73828 |
rs212889399 | in-del | -/GAATTACA | | | intron-variant | Dcaf4 | Mm_Celera | 12:83521166 | GATCTCCTCCAGCTG[-/GAATTACA]GATGATCGTGAGCCG | 73828 |
rs212939208 | snp | A/G | | | intron-variant | Dcaf4 | Mm_Celera | 12:83528027 | TTAGGAGAGTCACGG[A/G]TATTTTCTGGGCCTC | 73828 |
rs212941708 | snp | A/G | | | intron-variant | Dcaf4 | Mm_Celera | 12:83534639 | CTTTCTTTAATTTTA[A/G]GGGGCGTGTATGTGT | 73828 |
rs213019425 | snp | C/T | | | intron-variant | Dcaf4 | Mm_Celera | 12:83539776 | AAGTAACTGTCTGTG[C/T]TTCTACCTACAGATC | 73828 |