SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6217738 | snp | A/G | 0.412562 | 0.189931 | intron-variant | Ube2g1 | Mm_Celera | 11:72672817 | TATTTATAGTGGTAT[A/G]TTAAACTGCATATTT | 67128 |
rs6311759 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Ube2g1, Gm34592 | Mm_Celera | 11:72605384 | AGGTCCTGAGTTCAA[A/T]TCCCAGCAACCACAT | 67128 |
rs6312859 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Ube2g1, Gm34592 | Mm_Celera | 11:72605587 | ATAAGACCCTCTGCA[G/T]GTCCAATTCTAGAGC | 67128 |
rs6314387 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Ube2g1, Gm34592 | Mm_Celera | 11:72605883 | AAAACAAACAAACAA[A/G]CAAGCAAAACAACTA | 67128 |
rs6410120 | snp | A/G | 0.5 | 0 | intron-variant | Ube2g1 | Mm_Celera | 11:72629300 | GAGAGGTGACTATTA[A/G]AGGCATAAACAAGTC | 67128 |
rs6410781 | snp | A/G | 0.5 | 0 | intron-variant | Ube2g1 | Mm_Celera | 11:72629449 | GACTTTGTGCTTCCT[A/G]GGCAACTGCTCTGTC | 67128 |
rs6411346 | snp | A/G | 0.5 | 0 | intron-variant | Ube2g1 | Mm_Celera | 11:72629542 | GAgggctggagaaat[A/G]gctcagtggttaaga | 67128 |
rs6411381 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72629562 | AGTGGTTAAGAGCAC[C/T]GACTTCTCTTCCAGA | 67128 |
rs6411386 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72629567 | TTAAGAGCACCGACT[A/T]CTCTTCCAGAGGTCC | 67128 |
rs13471557 | snp | A/G | | | utr-variant-3-prime | Ube2g1 | Mm_Celera | 11:72683605 | GTAATAAGTTGGCAA[A/G]CTCTGGCTGGAACTG | 67128 |
rs26887941 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Ube2g1, Gm34530 | Mm_Celera | 11:72685533 | GTAACTCAGGGACAA[C/T]TATTTCTGAACTTAT | 67128 |
rs26887942 | snp | G/T | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Ube2g1, Gm34530 | Mm_Celera | 11:72684916 | AACAACTTCGGTGAT[G/T]GGTAAAATTAGTACA | 67128 |
rs26887943 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B | Ube2g1, Gm34530 | Mm_Celera | 11:72684409 | TAGCATGCGCAGCTA[C/T]AGGCTTTCTACATCT | 67128 |
rs26887944 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72681968 | TATACCGCTTTACCT[A/T]GGTTCTTTAGTGTAT | 67128 |
rs26887945 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Ube2g1 | Mm_Celera | 11:72670641 | AATCTTTTATGGACT[G/T]TTTCTTACTGCTTAC | 67128 |
rs26887946 | snp | C/T | 0.5 | 0 | intron-variant | Ube2g1 | Mm_Celera | 11:72669430 | TGTGCTAACTTCACT[C/T]CTAAAGTTTGTATAC | 67128 |
rs26887947 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g1 | Mm_Celera | 11:72668696 | GACATGCTATTTTAC[C/T]CATCTTCACCTAGCA | 67128 |
rs26887948 | snp | G/T | 0.265928 | 0.249492 | intron-variant | Ube2g1 | Mm_Celera | 11:72668224 | AAGAACACTCCACAT[G/T]ATTTACAGTCTATGT | 67128 |
rs26887949 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ube2g1 | Mm_Celera | 11:72665942 | GTCTCCATATCTCAA[C/T]CTCAGCCCTTCTGTT | 67128 |
rs26887950 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72665822 | TACATAGTGAGATCC[C/T]GTCTCAAAATAAAGT | 67128 |
rs26887951 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Ube2g1 | Mm_Celera | 11:72663986 | ACTGAGCGGTTCCCT[A/G]TGGAAATGATTTTCC | 67128 |
rs26887952 | snp | A/C | 0.32 | 0.24 | intron-variant | Ube2g1 | Mm_Celera | 11:72662892 | ATGTAAGAAGACACA[A/C]CAATTACATCTGGAT | 67128 |
rs26887953 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Ube2g1 | Mm_Celera | 11:72662767 | GATTTGAGTTTTGGT[G/T]TTCTTTCAACTAAAA | 67128 |
rs26887954 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ube2g1 | Mm_Celera | 11:72661362 | TCACACAGTTTGGAA[C/T]CAGTGAAAGGCATGT | 67128 |
rs26887955 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2g1 | Mm_Celera | 11:72660712 | CTCAGAGTTGTGGTG[C/T]TCTTCCTGCCTTTTT | 67128 |
rs26887956 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Ube2g1 | Mm_Celera | 11:72659770 | ACTTTAGATATCAGC[A/G]TCTTGATAGTGTAGG | 67128 |
rs26887957 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2g1 | Mm_Celera | 11:72659310 | TAGAAATGCGAACTT[A/G]TCATTGTTGGCTGTT | 67128 |
rs26887958 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Ube2g1 | Mm_Celera | 11:72659008 | ACATAAAAGTTTCAA[A/G]TCTACTAAGAAGAGA | 67128 |
rs26887959 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Ube2g1 | Mm_Celera | 11:72658870 | CTCAGAACATGGTCT[A/G]ACTCTATAGCCTGGA | 67128 |
rs26887960 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ube2g1 | Mm_Celera | 11:72657632 | AAAGCGACAAAGTGA[C/T]ATTTCGGAAACTTTT | 67128 |
rs26887961 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ube2g1 | Mm_Celera | 11:72657516 | ATGAGCTTGAATAGG[C/T]TCAGTTTTGCTAGGT | 67128 |
rs26887962 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Ube2g1 | Mm_Celera | 11:72654052 | TAAGGTTCATTCACA[A/G]TTTCTGTCTTCATCT | 67128 |
rs26887963 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2g1 | Mm_Celera | 11:72651568 | GCTTCTTAATGGTGA[A/G]AGGGCCTAGAACACC | 67128 |
rs26887964 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ube2g1 | Mm_Celera | 11:72650709 | TTGGTTTTCTCACTT[C/G]CACTATGATCACTTC | 67128 |
rs26887965 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Ube2g1 | Mm_Celera | 11:72648049 | GTCAGGAGTCCAGAT[C/T]AGAAGAGGATGAATA | 67128 |
rs26887966 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Ube2g1 | Mm_Celera | 11:72644692 | CAAGTGCAGCATCTG[C/T]AAAGGGGATGTAGAT | 67128 |
rs26887967 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Ube2g1 | Mm_Celera | 11:72644206 | GTTAATGTGTGAGAT[C/T]ATTACTCTGACTTGG | 67128 |
rs26900568 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Ube2g1 | Mm_Celera | 11:72644131 | GAGACTGAAGATGGT[A/G]GACAATGTGCTCCTG | 67128 |
rs26900569 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g1 | Mm_Celera | 11:72643650 | TTTTGAGAAGATGGG[C/T]TCAAAACAGTTGCAG | 67128 |
rs26900570 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ube2g1 | Mm_Celera | 11:72643625 | ATGGCAAAAGGTGAA[A/G]CTGTTTTGTTTTTGA | 67128 |
rs26900571 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2g1 | Mm_Celera | 11:72642674 | TGAACATTAACGAAC[C/T]TTTGTAGTTTGTAGT | 67128 |
rs26900572 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Ube2g1 | Mm_Celera | 11:72638644 | TTTCAGGTAACTGCG[C/T]CCTTTTAGGTAGGAA | 67128 |
rs26900573 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2g1 | Mm_Celera | 11:72638155 | GAGAAGAATTGGATT[C/T]GAATCAAAGGCCAAT | 67128 |
rs26900574 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ube2g1 | Mm_Celera | 11:72636978 | CTATTAAAGCACATC[C/T]CACAAAGAAAGAGTT | 67128 |
rs26900575 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Ube2g1 | Mm_Celera | 11:72634420 | GTCTTGATATCTTAA[A/G]TCATAGGATCATGTA | 67128 |
rs26900576 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2g1 | Mm_Celera | 11:72633031 | AGCATTCTTTTTTTC[C/T]CAAGACTGCTGGATA | 67128 |
rs26900577 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ube2g1 | Mm_Celera | 11:72631856 | GAAGTATTTAGAACA[C/G]CTTGTCATAGTAAAT | 67128 |
rs26900578 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Ube2g1 | Mm_Celera | 11:72631255 | ATCCATATTAAGTGC[A/G]TCTAACAAAGCATAT | 67128 |
rs26900579 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Ube2g1 | Mm_Celera | 11:72622265 | CCTTTTCCTCTTAGC[C/T]TTCCTCAAACTGGAA | 67128 |
rs26900580 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Ube2g1 | Mm_Celera | 11:72618694 | ACCTACTTCTGCTTT[A/T]TCCCCCTCAAGTAGC | 67128 |
rs26900581 | snp | C/G | 0.396694 | 0.202437 | intron-variant | Ube2g1 | Mm_Celera | 11:72618503 | GAGAAGCCTGAGGTG[C/G]TAAAAATCTTCCTGA | 67128 |
rs26900582 | snp | C/G | 0.396694 | 0.202437 | intron-variant | Ube2g1 | Mm_Celera | 11:72618361 | TGCCGTGGTGTGGAT[C/G]TGGGTCAATTGCTGG | 67128 |
rs26900583 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72618345 | CTTCTGCAAATTCAC[C/G]TGCCGTGGTGTGGAT | 67128 |
rs26900584 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Ube2g1 | Mm_Celera | 11:72615848 | GAGAAAAAGGGTCAA[A/T]AAGGCCTCACATGGG | 67128 |
rs26900585 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72609969 | TGTTGAACTAGTAGT[G/T]TGCCAGTGATAAAAG | 67128 |
rs26900586 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Ube2g1, Gm34592 | GRCm38.p3 | 11:72608066 | CCGGCAGCGCGGGGT[C/T]CGCGGAGTTAGGGCA | 67128 |
rs26900587 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Ube2g1, Gm34592 | Mm_Celera | 11:72606755 | TGTGCTAATCACAAC[C/T]CTGCACTTTACTCAG | 67128 |
rs26900588 | snp | A/G | 0.33241 | 0.236027 | upstream-variant-2KB, intron-variant | Ube2g1, Gm34592 | Mm_Celera | 11:72606521 | TGGGAAATGGGCAAG[A/G]AGGTTGGATAAGGTT | 67128 |
rs26900589 | snp | C/G | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Ube2g1, Gm34592 | Mm_Celera | 11:72606125 | TCACAGAAGCTTCAT[C/G]CTTTTGTGGGTAGAA | 67128 |
rs26900590 | snp | A/C | 0.33241 | 0.236027 | upstream-variant-2KB, intron-variant | Ube2g1, Gm34592 | Mm_Celera | 11:72606074 | TTTATTACATGCCTA[A/C]CGGAATCTGCTCCTC | 67128 |
rs29383269 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72625650 | TTTTCTTTTTTTCTT[C/T]TGGGACACTGGTTGA | 67128 |
rs29384917 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72669173 | TTTAATTTACAAAAA[A/T]AGTAAAAGGAGGTTT | 67128 |
rs29389834 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72656868 | GACCCTGTCTAAAAA[A/T]CCAGAATGTTTATTT | 67128 |
rs29391363 | snp | C/G | 0.32 | 0.24 | intron-variant | Ube2g1 | Mm_Celera | 11:72611053 | GGAGCCGTAGTTGAC[C/G]CAATCAATGAAGTAT | 67128 |
rs29392021 | snp | A/C | 0.5 | 0 | intron-variant | Ube2g1 | Mm_Celera | 11:72631563 | GGTTCCCAGCATCCA[A/C]ATGGGGGATAAAAGG | 67128 |
rs29392760 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72652622 | TAACTTACCACCCTT[A/G]CCCAGAAGAGGTTGT | 67128 |
rs29393479 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2g1 | Mm_Celera | 11:72627612 | GCGTCCTCTGCAAGA[A/G]CAGCTAGTTCTCTTT | 67128 |
rs29393497 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72667641 | TTCATAACAATAGCA[A/G]CAATACTATGAAGTA | 67128 |
rs29393880 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72655464 | GACAAACTCATCAGT[A/G]TATATTTAGAGTATA | 67128 |
rs29394070 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2g1 | Mm_Celera | 11:72653741 | ATATTTTGAACTGCT[A/G]AGCAATCATGTGATA | 67128 |
rs29395282 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72657955 | CAGGGTTTGATAATA[C/T]GATGCAAGGAAAACC | 67128 |
rs29396546 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Ube2g1, Gm34592 | Mm_Celera | 11:72609015 | GGATGAAGGAATTAA[A/G]ATTTTTGACTTAGTA | 67128 |
rs29396750 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72632492 | ATTAAATTATAGCAG[C/T]TGTTTTGGGGGTTCA | 67128 |
rs29397042 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72670820 | CAGTGCCTATGGAGT[C/T]CAGAAGAGGGTGTCT | 67128 |
rs29397057 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72609772 | GGCTTTTTCTTTTTT[A/C]CTTTAGCATTTTTAA | 67128 |
rs29397105 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72668320 | AAACATCTTGAAAAA[C/T]GAAACAAAAAGACTG | 67128 |
rs29398024 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72681426 | CAGATTCAAGACCAG[C/T]GAGGAATATGTGAGA | 67128 |
rs29400172 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Ube2g1, Gm34592 | Mm_Celera | 11:72606726 | ACCACCTGAATCCGA[A/G]CCATTTATCAGGTTG | 67128 |
rs29401542 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72669175 | TAATTTACAAAAATA[A/G]TAAAAGGAGGTTTTG | 67128 |
rs29404521 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72617517 | CTGGCTCCTAGTTTA[C/T]TTTTTGTTTCTCGTT | 67128 |
rs29404820 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72622660 | AAATGTTATTTTAAA[A/T]TTTTTTTTAAAAAGA | 67128 |
rs29404993 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72632209 | CCCCACTTTGGGGGA[C/G]GACGACAATGTCTCA | 67128 |
rs29405160 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72624805 | CAGGGTTTGTTTGTG[A/T]AGACCTGGCTGTCCA | 67128 |
rs29405569 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72613163 | CTTTTATATTTTGGG[A/G]GGAGCCAAGTGGTTC | 67128 |
rs29408146 | snp | C/G | 0.32 | 0.24 | intron-variant | Ube2g1 | Mm_Celera | 11:72645086 | AGGTATTTTGGCTAG[C/G]ATCTCAATATACACA | 67128 |
rs29408209 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72680291 | TCTATTGCTGTGATA[A/G]CGAACTTTGATCAAA | 67128 |
rs29408389 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72612782 | TGCTAGCTGCCCTTA[C/T]AGAGGACCAGGGTTT | 67128 |
rs29408399 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72660193 | GAAGAGCAGTCAGTG[C/T]TTTTAACTGATGAGC | 67128 |
rs29409000 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72675269 | ATTAAAGGCACAGGC[C/T]ACCACACTTATTATT | 67128 |
rs29411119 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72635690 | AATTAACCTTGGTTG[A/G]TCTGTAAGTCAAACG | 67128 |
rs29412860 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72665911 | ACTGCCCCCCCCCAC[C/G]TTTGTGTGTGTGTGT | 67128 |
rs29414474 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72626097 | TTTTATCCTTCCCTC[C/T]CTCCCCCCTTTTTCC | 67128 |
rs29415503 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72646047 | TAGCCACTGTGCCAG[C/T]GCTGGGAACTGAACC | 67128 |
rs29416166 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2g1 | Mm_Celera | 11:72616641 | AAAAGATATTTGGTA[C/T]TAGTAGACATTAGGA | 67128 |
rs29416495 | snp | C/G/T | 0.32 | 0.24 | intron-variant | Ube2g1 | GRCm38.p3 | 11:72619266 | TGTCTTTTTTTTTTT[C/G/T]GGGGGGGGGGTTTTC | 67128 |
rs29417489 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72658123 | CATGGTGGAAGAAAA[A/T]AAAAAATAATATATA | 67128 |
rs29418618 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2g1 | Mm_Celera | 11:72640749 | GCTAATGATGATGAA[C/T]TAACCTAAACAACAA | 67128 |
rs29420222 | snp | A/G | 0.5 | 0 | intron-variant | Ube2g1 | Mm_Celera | 11:72669662 | TAATTTAGAGGGGTA[A/G]TGGCAACTTTTTAGC | 67128 |
rs29420477 | snp | A/T | 0.5 | 0 | intron-variant | Ube2g1 | Mm_Celera | 11:72669034 | CCCAGTATAGTTTTT[A/T]AAAAAAATCGAAAAG | 67128 |
rs29421863 | snp | A/G | 0.5 | 0 | intron-variant | Ube2g1 | Mm_Celera | 11:72647066 | AGACACACCAGAAGA[A/G]GGAGTCAGATCTTGT | 67128 |