SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6229055 | snp | C/T | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70483518 | tctggagagacaaca[C/T]ggatatctactcacg | 93836 |
rs6229105 | snp | A/C | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70483548 | gctagatagggatcc[A/C]acaaaagaccaaagt | 93836 |
rs6365891 | snp | A/G | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70460538 | TTCTGAAAAGAGTAT[A/G]AGAGGTAATTTTAAG | 93836 |
rs6367084 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf111 | GRCm38.p3 | 9:70460780 | CAGTCAGTGCTCTAC[C/T]TCCTGAGCCATCTCA | 93836 |
rs6383197 | snp | C/T | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70497901 | AGCAGTTCTCAAGTT[C/T]TTTGACTTTTTAAGC | 93836 |
rs6383880 | snp | C/T | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70498043 | TCACACACTAAAAAG[C/T]TAACATTTATAAATG | 93836 |
rs13480264 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Rnf111 | Mm_Celera | 9:70490493 | AATTGGAAGCCAAAG[A/G]GAAATCTCAGTAGAA | 93836 |
rs29591154 | snp | G/T | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70463046 | AAGGGAATCTAACCT[G/T]GCTTTGTATCAAGTT | 93836 |
rs29592510 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf111 | Mm_Celera | 9:70505233 | GGAAATAGATATGTG[A/G]AATGTTTGTTATTTA | 93836 |
rs29595968 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Rnf111 | Mm_Celera | 9:70489964 | ACAGTCATAAAAAAT[G/T]TCAGCATCATATGGA | 93836 |
rs29597087 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rnf111 | Mm_Celera | 9:70459462 | ACACTGTTTTAGATA[C/T]TCACTTGGATTATAA | 93836 |
rs29638447 | snp | C/T | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70439126 | CAGAAATTTGCCTGC[C/T]TCTGCCTCCCAAGTG | 93836 |
rs29639061 | snp | C/T | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70474262 | GCACAGGCTTATACT[C/T]CAGGGTGGTATGTAC | 93836 |
rs29639306 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | Rnf111 | Mm_Celera | 9:70504775 | TGCCCTCTACAAGTA[G/T]AATTCTATCGGGACT | 93836 |
rs29639776 | snp | A/G | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70446200 | TAGGTTCTGAAGATG[A/G]ACCTCAGGTCCTCAA | 93836 |
rs29645404 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Rnf111 | Mm_Celera | 9:70505364 | GTAAAAAATTAGGAG[A/G]AAATTTAGCAATAAA | 93836 |
rs29648431 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Rnf111 | Mm_Celera | 9:70429326 | TTATTCTTTTGCTTA[C/G]AGAGCTGGCAATGGT | 93836 |
rs29692262 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf111 | Mm_Celera | 9:70447901 | CTTTATTTCTAACAT[C/T]TAATTGCACGGCTTT | 93836 |
rs29696462 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf111 | Mm_Celera | 9:70480572 | CAGTAACCACATGGT[A/G]GCTCAAAACCATCTG | 93836 |
rs29732981 | snp | A/G | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70427976 | CTACTTTATAAGGTG[A/G]GCTAACAGGAGATGT | 93836 |
rs29736533 | snp | G/T | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70478468 | ATATGAAAAAGAAAT[G/T]AACCAAAAACCAAAT | 93836 |
rs29736534 | snp | C/T | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70435572 | ATGGCCATTTATGGC[C/T]ATCCAGTGTGTTGAG | 93836 |
rs29736543 | snp | G/T | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70436979 | GGAGTGGATCAACCT[G/T]AGCTTAGAGTGCTAC | 93836 |
rs29738250 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf111 | Mm_Celera | 9:70500599 | GAGCATTTCTTTCTA[A/G]AGAGCTGTCCTGATA | 93836 |
rs29790050 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf111 | Mm_Celera | 9:70447176 | ATATATATATAGAGA[G/T]AGAGAGAGAGAGAGA | 93836 |
rs29840297 | snp | A/G | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70488126 | TGCATGAAGCCCCAG[A/G]CTCATTATTCAGTTT | 93836 |
rs29841670 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf111 | Mm_Celera | 9:70504859 | GGCTTGGTTAGGTTT[A/G]GTTTTTTTCGAGACA | 93836 |
rs29842925 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf111 | Mm_Celera | 9:70451763 | ATAGTAAAGATCTTA[C/T]CCCTGAACAGTGTCA | 93836 |
rs29885188 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf111 | Mm_Celera | 9:70494250 | AATCTGAAGAAAAAA[A/G]CACCAAATAAATGAC | 93836 |
rs29887468 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70440988 | TTCTTAACTTATAAA[G/T]CTAAAGCAAATAGAA | 93836 |
rs29888102 | snp | A/T | 0.5 | 0 | intron-variant | Rnf111 | GRCm38.p3 | 9:70499113 | TCTCTCTTTTTTTTT[A/T]AAAAAGATTTATTTA | 93836 |
rs29931009 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Rnf111 | GRCm38.p3 | 9:70462292 | TAAATGATAACCCCC[A/C/T]AAATTTTTATTCTTT | 93836 |
rs29934025 | snp | C/T | 0.401235 | 0.199068 | synonymous-codon | Rnf111 | Mm_Celera | 9:70443509 | AATATGGTGTGAAAT[C/T]GGCTGGTGAGCAGGA | 93836 |
rs29940825 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf111 | Mm_Celera | 9:70501803 | CCCAACTCACAAATG[C/T]CCTCAGTAATTTTTT | 93836 |
rs29979669 | snp | A/G | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70497554 | CTATACCAAGGAGGG[A/G]AAAAAAAAAAAAAAA | 93836 |
rs29986285 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70432866 | CTGACCACAAGGTCA[C/T]TAATTCCTTCATTCA | 93836 |
rs29986719 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rnf111 | Mm_Celera | 9:70501791 | CACTATCATTCACCC[A/T]ACTCACAAATGTCCT | 93836 |
rs29988500 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70436114 | GCCTCCTAAGTGCTA[A/G]GATTAAAGGCGTGCA | 93836 |
rs29994406 | snp | G/T | 0.492188 | 0.0620098 | intron-variant | Rnf111 | Mm_Celera | 9:70447014 | GTTCTTCCTAAAAGC[G/T]CCACTTGTCATAGAG | 93836 |
rs30024562 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf111 | Mm_Celera | 9:70471782 | TATCAGTCACTAGCC[C/T]ACAATGCTAACACAC | 93836 |
rs30030100 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rnf111 | Mm_Celera | 9:70491065 | GGCACATGCTTGTAA[A/T]CCCAGCAACTGAGAG | 93836 |
rs30031723 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf111 | Mm_Celera | 9:70431758 | TTTATATAGTTACTT[C/T]TGACCTTAAGATATT | 93836 |
rs30080840 | snp | C/T | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70466121 | GACAGATACCAGGTA[C/T]CAAAGTTAAATCAGG | 93836 |
rs30093036 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Rnf111 | Mm_Celera | 9:70491319 | GGCACCACAGTTATA[G/T]GTTAACGGGGAGCCA | 93836 |
rs30125066 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf111 | Mm_Celera | 9:70483603 | GGTGAACCCACGAAT[G/T]TTATTGGCGTTTCTT | 93836 |
rs30137944 | snp | C/T | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70459543 | TATTAGAAGGTGTGG[C/T]CCTGTTGCAGTAAAT | 93836 |
rs30141149 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf111 | Mm_Celera | 9:70473234 | CAAAATACCACCTCG[A/T]GATTTTAAACAGACA | 93836 |
rs30144481 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Rnf111 | Mm_Celera | 9:70473332 | AATTACATAAAACAA[C/G]CCTGAGTGCCTCCCT | 93836 |
rs30162990 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70478004 | TTTCAATGGCTATAG[A/T]AGCACTATATATGAA | 93836 |
rs30185978 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf111 | Mm_Celera | 9:70498788 | GATTCTTAAACTTTC[C/T]ATTGGTAGACAGCCA | 93836 |
rs30187830 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB | Rnf111 | Mm_Celera | 9:70504899 | TGTATTGCCCCGGCT[G/T]TCCTGGAACTCACTC | 93836 |
rs30219144 | snp | C/T | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70454645 | ATTCAAGTATATGCA[C/T]AGGCTACAAAAGTGA | 93836 |
rs30234044 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70489142 | GAAAGCAAGCAAGCA[A/T]GCATGCATGCATAGA | 93836 |
rs30234124 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Rnf111 | Mm_Celera | 9:70485930 | TATTAATGCAGGCCA[A/G]TTATATTTACAGACT | 93836 |
rs30236616 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Rnf111 | Mm_Celera | 9:70444110 | GTATACATTCTTACC[A/G]TCACAGTCAGCAATG | 93836 |
rs30276904 | snp | G/T | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70500988 | GTTTTGTTTTGTTTT[G/T]TTTGTTTTTCGAGAC | 93836 |
rs30280695 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70444388 | GTTTATTTTTATAAC[A/G]TGTATAAGTGCCCTT | 93836 |
rs30283554 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Rnf111 | Mm_Celera | 9:70505084 | CCAAAGGCTTGAACT[C/T]AGTTGGTTGTTGAGT | 93836 |
rs30327001 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf111 | Mm_Celera | 9:70491384 | CCTTTTAACAAGTAG[G/T]AACTATTGTCAAAGA | 93836 |
rs30330989 | snp | G/T | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70447172 | ATATATATATATATA[G/T]AGAGAGAGAGAGAGA | 93836 |
rs30331479 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70444254 | CATGACAGAAGAGGA[A/C]ATCAGATCCTACTAC | 93836 |
rs30332025 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70499404 | AGTAACTCTAAAACA[C/T]GGCTGTGCCACCTTT | 93836 |
rs30333679 | snp | A/G | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70462183 | TCTCTCTCTAACCCT[A/G]GTTCCAGGGGACCCG | 93836 |
rs30338007 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70498323 | TCTGAAGCTGTAATA[A/G]TCAAACTTTTCAATA | 93836 |
rs30370459 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70499324 | ATTCTTCAGTCTCTA[C/G]CTCTAAAATCTAGAC | 93836 |
rs30370879 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70449531 | AATGCACAGAACCAC[C/T]ATAAAAGACAGCTTC | 93836 |
rs30425426 | snp | A/G | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70470071 | CTTTGACCTTCACAC[A/G]CACACCCAACCACCC | 93836 |
rs30425754 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf111 | Mm_Celera | 9:70484372 | AAGGATCAATAAAAA[A/G]AATTGAAAAATAAGT | 93836 |
rs30425787 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70499350 | TAGACATGTTCCTAC[A/G]TAAGTAAACATATTA | 93836 |
rs30455381 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Rnf111 | GRCm38.p3 | 9:70470268 | AACCTGTAAAATGTG[A/G/T]AAACAGGTAGATACT | 93836 |
rs30473894 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf111 | Mm_Celera | 9:70486667 | GCAGCTGCTATTTCA[C/T]ATCAGGTTATACACA | 93836 |
rs30482727 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Rnf111 | Mm_Celera | 9:70429395 | TAAATACATGCCCTC[A/G]TGACCAGTTGATCCA | 93836 |
rs30503392 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70444359 | GGAAAGCCATCTCTC[C/T]AATGTGTGTGTGTGT | 93836 |
rs30521047 | snp | A/G | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70471598 | CCAAATAATAAAGAC[A/G]CATTAGGAGAGAACT | 93836 |
rs30523049 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70432875 | AGGTCACTAATTCCT[C/T]CATTCAATTTAATAT | 93836 |
rs30524716 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70489114 | GAAAGAAAGAAAGAA[A/C]GAAAGAAAGAAAGAA | 93836 |
rs30527116 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rnf111 | Mm_Celera | 9:70451673 | GCTGTAGTTTTCAAA[A/T]TGGATTTGACCAAGT | 93836 |
rs33630186 | snp | A/T | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70479528 | CCTGTAAATGGAAGC[A/T]CTTGTTTATCCTTGT | 93836 |
rs33633449 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf111 | Mm_Celera | 9:70472825 | TGCTTGCTTTCTTGC[C/T]TTTCTTTTTTTATGT | 93836 |
rs33636265 | snp | A/G | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70483647 | AGAGGTTGCTTACAG[A/G]AGCAGAATGACTCAA | 93836 |
rs33638796 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf111 | Mm_Celera | 9:70472875 | TGTATATAATGTATA[G/T]AAGGATGTGACTAAT | 93836 |
rs33660926 | snp | A/G | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70487902 | AAGGCCGGGCAGTGG[A/G]GAGGCAGAGGCAGGC | 93836 |
rs33676161 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Rnf111 | Mm_Celera | 9:70429159 | GCCCTTATAATCCAG[A/G]TATCAAAATCCTTTC | 93836 |
rs33678070 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf111 | Mm_Celera | 9:70497553 | ACTATACCAAGGAGG[A/G]GAAAAAAAAAAAAAA | 93836 |
rs33686670 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70445403 | GCTGGCCTGGAACTC[A/C]AGAGATCTACTTGCC | 93836 |
rs33711153 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70481490 | TGTGGAGAGAGAAAA[G/T]GCATCACTGTCTACC | 93836 |
rs33713900 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Rnf111 | Mm_Celera | 9:70441749 | CTGAGATACTCAAAA[A/C]TGATTATAAAGTGCT | 93836 |
rs33726715 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Rnf111 | Mm_Celera | 9:70479224 | TCAGTGGTTAAGAAC[A/C]CAGACTGCTCTTCCA | 93836 |
rs33727378 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf111 | Mm_Celera | 9:70456397 | TAACTCCAGTTCCAG[A/G]GGAATCTAATGTCCT | 93836 |
rs33730414 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70474526 | GGTGACACATTACAC[A/G]ATTGTAATCCCAGCA | 93836 |
rs33739468 | snp | G/T | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70456446 | ACCAAGTTTTTTGTT[G/T]GTTTGTTTTTGTTTT | 93836 |
rs33747334 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf111 | Mm_Celera | 9:70447174 | ATATATATATATAGA[G/T]AGAGAGAGAGAGAGA | 93836 |
rs33755042 | snp | A/G | 0.5 | 0 | intron-variant | Rnf111 | Mm_Celera | 9:70447587 | TGGTCTACAGAATTA[A/G]TTCCAGGACAGCCAT | 93836 |
rs33756801 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf111 | Mm_Celera | 9:70429929 | TGTTAATTCATGATG[G/T]TGATACTCTGTATAA | 93836 |
rs33765122 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf111 | GRCm38.p3 | 9:70434154 | GTCCCTCTTTTTTTT[A/T]AAAAAAAAAAAAAAA | 93836 |
rs33765229 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf111 | Mm_Celera | 9:70463365 | CCCAGGGGAGTCTAC[A/G]GACACCCACAAGGAC | 93836 |
rs33779165 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf111 | Mm_Celera | 9:70502030 | GGATTAAAGGCAACT[C/G]GAGCCATCACACACT | 93836 |
rs36250197 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Rnf111 | Mm_Celera | 9:70427262 | CAGGATGGCTCAGTG[C/G]GCAAAGTAATTGCTG | 93836 |
rs36341125 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rnf111 | Mm_Celera | 9:70444931 | ACACTTCTATTGCTG[C/T]CCTTGCCTTTCCACA | 93836 |
rs36361237 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf111 | Mm_Celera | 9:70454457 | TCATTTTCTCTTCTG[C/T]CCAAACTCAGATAAA | 93836 |