SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6153904 | snp | A/G | 0.5 | 0 | intron-variant | Ube2w | Mm_Celera | 1:16579898 | ggagacagtggtgct[A/G]acgcagactgagccc | 66799 |
rs6154478 | snp | C/T | 0.5 | 0 | intron-variant | Ube2w | Mm_Celera | 1:16580001 | acaatgtggctattt[C/T]ctgctcttgtccaaa | 66799 |
rs6160159 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ube2w | Mm_Celera | 1:16547722 | TACTAAGTATATAGT[A/G]AGTAAAAAAGGCAAA | 66799 |
rs6175597 | snp | A/T | 0.5 | 0 | intron-variant | Ube2w | Mm_Celera | 1:16548165 | GCCAGGAAGTACTTA[A/T]CACAGATGTTTAATC | 66799 |
rs6175667 | snp | A/G | 0.5 | 0 | intron-variant | Ube2w | Mm_Celera | 1:16548202 | TACCATCCTAGAATA[A/G]TATTTAAAATTGATA | 66799 |
rs13465201 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | Ube2w | Mm_Celera | 1:16570545 | TATACTCCTCAGTCT[C/T]TGAAGTGAAGGTGTG | 66799 |
rs30469187 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16544909 | TGTAATTTTGCTACT[G/T]TTATGAGTTACAACA | 66799 |
rs30599754 | snp | A/C | 0.265928 | 0.249492 | intron-variant | Ube2w | Mm_Celera | 1:16560781 | TTCACACCAATGAGC[A/C]GACATTTTTGAAACC | 66799 |
rs30617262 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Ube2w | Mm_Celera | 1:16619624 | CAGCCCACCCCCTTC[A/G]TATGTCTTTTTTACA | 66799 |
rs30770483 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16608527 | TTCTAGTCAACTGCA[C/T]GTGTGTACATAATTG | 66799 |
rs30865162 | snp | A/C | 0.32 | 0.24 | intron-variant | Ube2w | Mm_Celera | 1:16558386 | TAGAGCTGTTCAAAG[A/C]GGTTGTGAACCACTC | 66799 |
rs30916861 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16563868 | TAGAAAAACAGATGC[C/T]GGGGGCTGGAGAGAT | 66799 |
rs31044459 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16612245 | TACATATATCAGAGA[A/G]AGAGAGAGAGAGAGA | 66799 |
rs31051335 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Ube2w | Mm_Celera | 1:16557885 | TTTTTATTTGTTTTA[C/T]TAATGCTCACAATAA | 66799 |
rs31105679 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2w | Mm_Celera | 1:16567379 | AAAGGCATCAGAGGT[C/T]ACACTGGAGCAGCAC | 66799 |
rs31292858 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16601125 | AACTACTACTTTTTT[A/T]AAAAAGGTAATTTGG | 66799 |
rs31331969 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Ube2w | Mm_Celera | 1:16582142 | ACACAAGTAGCATGT[C/T]GGCCTCGATGGTTTT | 66799 |
rs31348249 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Ube2w | Mm_Celera | 1:16586457 | GCGGTTGCTCCTACC[C/T]AGTGATCACACTGTA | 66799 |
rs31360935 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16548815 | AAACAGACCCCCCCA[A/C]AAAAAAATTAGGAAG | 66799 |
rs31368459 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ube2w | Mm_Celera | 1:16581743 | CTAATTTTACTTCTC[C/T]TATGATAGGTATGAT | 66799 |
rs31388313 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16548816 | AACAGACCCCCCCAA[A/C]AAAAAATTAGGAAGA | 66799 |
rs31397826 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2w | Mm_Celera | 1:16599045 | TGTGAGCTTGTTTCA[C/T]TGGTACTCTGTAACC | 66799 |
rs31427458 | snp | A/C/T | 0.265928 | 0.249492 | intron-variant | Ube2w | GRCm38.p3 | 1:16566048 | CTGAGCTTGCCATCC[A/C/T]GAGCACACTCTACTG | 66799 |
rs31457867 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16548783 | AGAGAAACCCTGTCT[C/T]GAAAAACCAAAAAAC | 66799 |
rs31517465 | snp | A/G | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Ube2w, Gm31780 | Mm_Celera | 1:16596740 | ACAGACGCCTTTATA[A/G]TGACAGGTCATGGCA | 66799 |
rs31553969 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Ube2w | Mm_Celera | 1:16556990 | GCCAGCCATTCTGTA[C/T]TGTTACTAATATTAT | 66799 |
rs31557961 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16585631 | GGGAGGAGCCCACAG[A/G]CTGTTTCATAGATTG | 66799 |
rs31615824 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Ube2w | Mm_Celera | 1:16548305 | CAATGTAAAGGAGCT[C/G]GTATATAGCTCAGTG | 66799 |
rs31644947 | snp | A/C | 0.475309 | 0.108333 | intron-variant | Ube2w | Mm_Celera | 1:16599206 | GTAGCTGGCCAAATC[A/C]TTTCACTTCATACTT | 66799 |
rs31689315 | snp | G/T | 0.32 | 0.24 | intron-variant | Ube2w | Mm_Celera | 1:16605469 | CCCATTTCCTAGCAG[G/T]GGATGGCTGCTCTTG | 66799 |
rs31712739 | snp | A/G | 0.456747 | 0.140554 | intron-variant, utr-variant-3-prime | Ube2w, Gm31780 | Mm_Celera | 1:16595932 | TATGAAATTTTAGAA[A/G]GGTATGTACCCACAG | 66799 |
rs31716363 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2w | Mm_Celera | 1:16549736 | GAAGAGACACCATGA[C/T]CAAGGAAACTCTTAT | 66799 |
rs31721965 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2w | Mm_Celera | 1:16618377 | ATTGGATTTGCAAGG[G/T]GGGGGGGGATACATT | 66799 |
rs31729304 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16610009 | ACAAAAAAAAAAAAA[A/G]AGAGAGAGAGAGAGA | 66799 |
rs31731549 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2w | Mm_Celera | 1:16555974 | GCTGCCATGCTCCTT[G/T]CCTTGCTGGTCCTGG | 66799 |
rs31795687 | snp | A/G | 0.444444 | 0.157135 | intron-variant, utr-variant-3-prime, nc-transcript-variant | Ube2w | Mm_Celera | 1:16569236 | TTAACTTACAGCTGT[A/G]ATTTCATCGTAAAAG | 66799 |
rs31825557 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16580734 | TAGTCAACAAAGCTG[A/G]AAGGAGTTAGAGATC | 66799 |
rs31834648 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16561022 | CCATGGGAACTGAAG[A/G]TACAGATGGTCGTAA | 66799 |
rs31874472 | snp | C/G | 0.387812 | 0.208586 | intron-variant | Ube2w | Mm_Celera | 1:16582272 | CTTAACCAAGGTTGT[C/G]TGAAGAACTACAGCA | 66799 |
rs31908574 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16585623 | CATGCAGTGGGAGGA[A/G]CCCACAGGCTGTTTC | 66799 |
rs31927892 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2w | GRCm38.p3 | 1:16549638 | AGAAGAAGAAGAAGA[A/G]GAAGAAAGGTAACTT | 66799 |
rs31946938 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2w | Mm_Celera | 1:16567857 | GAGGCAGGCGGATTT[C/T]TGAATTCGAGGCCAG | 66799 |
rs31957588 | snp | A/T | 0.32 | 0.24 | intron-variant | Ube2w | Mm_Celera | 1:16558474 | CCACTGAACTATCTC[A/T]CCAGTCCCTCCTCTA | 66799 |
rs31957589 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Ube2w | GRCm38.p3 | 1:16602811 | CTGCTGAGCCATCTC[A/C/G]CCAGCCCAGGTACAG | 66799 |
rs31972990 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16572344 | CGGGGCCGACCGGAG[C/T]GAGCAGAGGTCCTAA | 66799 |
rs32044975 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16577278 | GCCATCCCGCCCGCC[C/T]CCCCCAATCCTAGCA | 66799 |
rs32133326 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16614022 | CTGAATGTTAAGAGT[C/T]CTTTGTTTTGTTCTA | 66799 |
rs32193172 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2w | Mm_Celera | 1:16620109 | AGTGAGCTTGAGTAG[A/G]AATCGCTGAGCATAC | 66799 |
rs32203433 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ube2w | Mm_Celera | 1:16549131 | CAATGCTGCCTGGAA[A/G]TGTTAGTTGCCCAGC | 66799 |
rs32221674 | snp | C/G | 0.432133 | 0.171253 | intron-variant, utr-variant-5-prime | Ube2w, Gm31780 | Mm_Celera | 1:16591798 | TACTACCTCTCAAGA[C/G]CAGTTCCACCACCAG | 66799 |
rs32226840 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16617070 | CCTAGGGTAAGATGA[A/G]TTAATGAACACATTT | 66799 |
rs32274720 | snp | A/G | 0.5 | 0 | intron-variant | Ube2w | Mm_Celera | 1:16576418 | CACTCAATCTCTCAA[A/G]ACTAAAATGCTAGCT | 66799 |
rs32284811 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2w | Mm_Celera | 1:16567935 | ACCCTGTCTCGAAAA[A/C]CCAAAAAAAAAAAAA | 66799 |
rs32296936 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16581553 | CTTCAGCCAATCACA[A/G]TGATATACATCTATA | 66799 |
rs32314760 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Ube2w | Mm_Celera | 1:16541547 | GATCTCCAAAGGCCA[A/G]ACTGGAAACAGAATT | 66799 |
rs32317821 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ube2w | Mm_Celera | 1:16581838 | ATGTTACCTCAATTA[C/T]ATCCTCTCACTACTT | 66799 |
rs32332861 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2w | Mm_Celera | 1:16567671 | AAAAAACAAAAAAAA[A/C]CAAAAAACAAAAACA | 66799 |
rs32335340 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16542521 | TCCCCCACCTCCATA[A/G]TCCTCTCATTTGAGA | 66799 |
rs32363398 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2w | Mm_Celera | 1:16581825 | TAATATTACAAAAAT[A/G]TTACCTCAATTACAT | 66799 |
rs32373889 | snp | A/T | 0 | 0 | intron-variant, utr-variant-3-prime | Ube2w, Gm31780 | Mm_Celera | 1:16595877 | CACAGAGAAACACTC[A/T]CTTTCTTGGGGGAGG | 66799 |
rs32375817 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16618828 | CCGTCCTCGGCGAGG[C/G]GCTCTGCCGGTCTCC | 66799 |
rs32378673 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB, utr-variant-5-prime | Ube2w | Mm_Celera | 1:16619395 | GTGTCCGATTGGCTA[A/G]CGCGCGGGTGCCCGG | 66799 |
rs32403545 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2w | Mm_Celera | 1:16567408 | ACACGGCATGACAGC[A/G]GCTGCCTGTGTGCTC | 66799 |
rs32412222 | snp | A/G | 0.5 | 0 | intron-variant | Ube2w | Mm_Celera | 1:16585849 | TAGCCCGGGCTACAC[A/G]CTGAAAGCATATTTA | 66799 |
rs32427719 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2w | Mm_Celera | 1:16583297 | TTCAGTAGGGAGGGG[A/G]AAAAAATGAAGCATC | 66799 |
rs32448798 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16548814 | TAAACAGACCCCCCC[A/C]AAAAAAAATTAGGAA | 66799 |
rs32460762 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16577277 | TGCCATCCCGCCCGC[C/G]TCCCCCAATCCTAGC | 66799 |
rs32492144 | snp | A/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Ube2w, Gm31780 | Mm_Celera | 1:16591013 | CGTTTGGAAGCTGAT[A/T]ATGGGGTGGATCCCT | 66799 |
rs32500763 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16557932 | CTTAGAACATCCTTG[A/G]CTGTACTCCAAATGT | 66799 |
rs32610619 | snp | A/G | 0.375 | 0.216506 | intron-variant, utr-variant-5-prime | Ube2w, Gm31780 | Mm_Celera | 1:16591521 | AAAACTAGAAAGAAG[A/G]GGGAGAATGGGGGCG | 66799 |
rs32613919 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2w | Mm_Celera | 1:16548625 | AAATGTGAAGACAGC[C/T]CATGTTTAGAATCAG | 66799 |
rs32645752 | snp | A/T | 0.265928 | 0.249492 | intron-variant | Ube2w | Mm_Celera | 1:16562896 | CCACCTGATACCTTC[A/T]TCACCTGAACCCCAA | 66799 |
rs32688719 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Ube2w | Mm_Celera | 1:16582295 | CTACAGCAACTTTCA[A/G]GTATCCACATAGGCT | 66799 |
rs32732272 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2w | Mm_Celera | 1:16583063 | CATGGTGGCTCACAA[C/T]GGATGCCCTCTTCTG | 66799 |
rs32753841 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2w | Mm_Celera | 1:16574000 | GGTTACCTCCATCAC[C/T]ACTGACATCACTGAG | 66799 |
rs32800760 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Ube2w | Mm_Celera | 1:16541549 | TCTCCAAAGGCCAAA[C/T]TGGAAACAGAATTGA | 66799 |
rs45671003 | snp | A/T | | | intron-variant | Ube2w | Mm_Celera | 1:16577881 | GGGAAAAGAAAGCAT[A/T]AAAAAACCAGAGAGC | 66799 |
rs45695237 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2w | Mm_Celera | 1:16565540 | GTCCTGAATTATTAG[C/T]GTTTGCAGAGTCGTT | 66799 |
rs45776676 | snp | A/C | | | intron-variant | Ube2w | Mm_Celera | 1:16547804 | TGGAATAGATGTATC[A/C]CCATGGGCATGGGCT | 66799 |
rs45782714 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ube2w | Mm_Celera | 1:16574335 | AGTAATTTTGTAGCC[A/G]TAAAAGGTAAAACAA | 66799 |
rs45877597 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2w | Mm_Celera | 1:16561256 | AGGCATGCTATAGAC[A/G]TAGCCTTAGCTAAAA | 66799 |
rs45989484 | snp | A/G | | | intron-variant | Ube2w | Mm_Celera | 1:16561900 | CAAAAACAAACCAGG[A/G]GGGATATCCTAGCTA | 66799 |
rs46009862 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ube2w | Mm_Celera | 1:16586009 | GGTGAAATAGAAAAT[A/T]ATAAGGCAGAGTCTA | 66799 |
rs46058757 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2w | Mm_Celera | 1:16587226 | ATGGGCTGTTTGCCT[A/G]TGAACAGCTGTTCTA | 66799 |
rs46062481 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2w | Mm_Celera | 1:16566836 | GTTTTGTCAATTAGT[C/T]GATACATTTAGCTAC | 66799 |
rs46094946 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2w | Mm_Celera | 1:16578017 | TACAGTAACAATAAG[A/G]AGCTGTTGCTCACAA | 66799 |
rs46116019 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ube2w | Mm_Celera | 1:16586052 | TTGCGTCTTCCTCTG[C/T]CTACTCCCTCAAGTC | 66799 |
rs46131084 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2w | Mm_Celera | 1:16563157 | ATGTAGTTTTTAACC[C/G]TATGTGTGTCAGACC | 66799 |
rs46160625 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ube2w | Mm_Celera | 1:16575812 | AGACAAATGCCTGTG[C/T]TAAGTGGCAACAAGG | 66799 |
rs46200747 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Ube2w | Mm_Celera | 1:16566142 | ATAATTCAATAATCT[A/C]CCCAAATCGTTCTGT | 66799 |
rs46214479 | snp | G/T | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Ube2w, Gm31780 | Mm_Celera | 1:16591607 | ATCTCCTAAAGCCTA[G/T]GAAACAGTCGCCTCC | 66799 |
rs46243209 | snp | A/G | 0.336735 | 0.234472 | intron-variant, utr-variant-5-prime | Ube2w, Gm31780 | Mm_Celera | 1:16591963 | TGATTCAACCTCTAA[A/G]AAGGTGCAAGCTGTG | 66799 |
rs46256246 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2w | Mm_Celera | 1:16565790 | TCTCATACTTATCCA[A/G]TTAGTATTCAAGTAT | 66799 |
rs46276295 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2w | Mm_Celera | 1:16563255 | GGCAAGGAATTTTGT[C/T]TCTGGGTTAAGGTAA | 66799 |
rs46291380 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2w | Mm_Celera | 1:16579277 | AAGTCTATACATTAC[C/T]CCCAGAACAAGGAAA | 66799 |
rs46292848 | snp | A/G | | | intron-variant | Ube2w | Mm_Celera | 1:16562369 | TTACGTCTTCAACCC[A/G]CTCTCCCCTTGAATA | 66799 |
rs46326802 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2w | Mm_Celera | 1:16586563 | CACCACAGGGGCACC[C/T]TCTGCAAAGTCTGAG | 66799 |
rs46343975 | snp | A/G | | | intron-variant | Ube2w | Mm_Celera | 1:16577869 | CAGGGTTCACGTGGG[A/G]AAAGAAAGCATAAAA | 66799 |
rs46360171 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ube2w | Mm_Celera | 1:16561444 | ATTATGATATGTAAC[A/C]AAAGGCATATGACAT | 66799 |
rs46385029 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2w | Mm_Celera | 1:16573094 | ACAATGCCCTCCAAA[C/G]TAGATGGATTATAAG | 66799 |