SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs29320250 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2d1, Gm34376 | Mm_Celera | 10:71285740 | CTTCCTTCCTTCCTT[C/T]CTTTCTTTCTTTCTT | 216080 |
rs29366636 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2d1 | Mm_Celera | 10:71267158 | AAACAAACCAAAAAC[A/G]ACTTAGTGACGTAAC | 216080 |
rs29937675 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2d1 | Mm_Celera | 10:71261224 | TGAACACTGAGCCGG[A/G]AAAGAACTTACGTTC | 216080 |
rs29937677 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Ube2d1 | Mm_Celera | 10:71261370 | TCCCCCAGTTTGGAT[G/T]ATAGGGCAAACGATT | 216080 |
rs29937679 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2d1 | Mm_Celera | 10:71261605 | GCAGTCGGTTTAAGG[C/T]AAAGCAGCAAACTCA | 216080 |
rs29937681 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2d1 | Mm_Celera | 10:71261616 | AAGGTAAAGCAGCAA[A/G]CTCAAAAGGTGACAG | 216080 |
rs29937683 | snp | A/C | 0.32 | 0.24 | intron-variant | Ube2d1 | Mm_Celera | 10:71261700 | GCAAACCGATGCTGG[A/C]CGGATGGAGCAGTTC | 216080 |
rs29938655 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Ube2d1 | Mm_Celera | 10:71261755 | AACCTCTGAGAACTG[A/T]GGATGTGTGAGGAAG | 216080 |
rs29938657 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2d1 | Mm_Celera | 10:71261778 | TGAGGAAGACTCCAC[C/T]TCCTTTAAAAACAAC | 216080 |
rs29938659 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2d1 | Mm_Celera | 10:71261945 | GAAATCACTGCAAAC[C/T]CTCAATCAGGTTTTG | 216080 |
rs29938661 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Ube2d1 | Mm_Celera | 10:71262303 | GTTAATCCTTCCATT[A/T]CCAGGGAAACAGGCA | 216080 |
rs29938663 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2d1 | Mm_Celera | 10:71263087 | AAAATAATCAGGCCA[C/T]GTCTGAAACCTACAA | 216080 |
rs29939565 | snp | C/G/T | 0.231111 | 0.249285 | intron-variant | Ube2d1 | Mm_Celera | 10:71263876 | TATACCTGAAGAACC[C/G/T]GGTTTAGTATGGAAG | 216080 |
rs29939567 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2d1 | Mm_Celera | 10:71264412 | GTCAACCTCAGAGGT[A/G]GGTGTCAGCACATCC | 216080 |
rs29939569 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2d1 | Mm_Celera | 10:71264494 | GATGTGCAAAGATTC[A/G]TTTACTGAGGTAGGG | 216080 |
rs29939571 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2d1 | Mm_Celera | 10:71264845 | TCTTCCTTCTGAGCC[A/G]CGTCCCTTCAATGCT | 216080 |
rs29939573 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2d1 | Mm_Celera | 10:71265013 | TTTAACATTGAAGCC[C/T]GGGCACCACCCCTCA | 216080 |
rs29940359 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B | Ube2d1 | Mm_Celera | 10:71254484 | AGATCAGAACTGTTC[C/T]TTAGGGTAGGGAATA | 216080 |
rs29940361 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B | Ube2d1 | Mm_Celera | 10:71254570 | ACCCCAGCGTCTAAA[C/T]TCTCATCTCCAATGA | 216080 |
rs29940363 | snp | C/G | 0.231111 | 0.249285 | downstream-variant-500B | Ube2d1 | Mm_Celera | 10:71254627 | AGACAGTCTGATAAA[C/G]AGGATGCTGACCTGC | 216080 |
rs29940385 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2d1 | Mm_Celera | 10:71265646 | TAAATCAGGTATAGA[C/T]GCAAATGCACACTAA | 216080 |
rs29940387 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2d1 | Mm_Celera | 10:71265653 | GGTATAGATGCAAAT[A/G]CACACTAATTACTTT | 216080 |
rs29940389 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2d1 | Mm_Celera | 10:71265745 | AATCTCAAATGTCAA[A/G]CTGTTCTTCAAATCT | 216080 |
rs29940391 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ube2d1 | Mm_Celera | 10:71266220 | ACAGACAGCAAGGGT[G/T]CGAGACACACGTTCC | 216080 |
rs29940393 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ube2d1 | Mm_Celera | 10:71266457 | CAAGGGTTGCTGAGC[C/G]ATATGCTCTTTCCAA | 216080 |
rs29941275 | snp | A/C/T | 0.132653 | 0.220748 | intron-variant | Ube2d1 | Mm_Celera | 10:71266493 | CTTACAATCCGAGCG[A/C/T]GTGGTACTTTCTCTG | 216080 |
rs29941277 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Ube2d1 | Mm_Celera | 10:71266630 | TCAGCTACTTAATCA[A/C]TGCAGAGACATTTAA | 216080 |
rs29941279 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2d1 | Mm_Celera | 10:71267425 | TCAGTTCCCTAAGAG[C/T]TAACACTGAATCATA | 216080 |
rs29941281 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2d1 | Mm_Celera | 10:71267475 | GGGTCCTCATGTGAG[C/T]TGACAGCGCTGTAAA | 216080 |
rs29941283 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2d1 | Mm_Celera | 10:71267590 | CCATGTGCAGCCAAA[A/G]GAGCTCGGAGTACTC | 216080 |
rs29941305 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B | Ube2d1 | Mm_Celera | 10:71254816 | CCTCTGATCTTCACC[A/G]CCAACTAAATAAGTG | 216080 |
rs29941307 | snp | A/G | 0.132653 | 0.220748 | downstream-variant-500B | Ube2d1 | Mm_Celera | 10:71254938 | CAATCCTGAAGAATA[A/G]ATCAAGCAGTTTTGA | 216080 |
rs29941309 | snp | A/C | 0.231111 | 0.249285 | utr-variant-3-prime | Ube2d1 | GRCm38.p3 | 10:71255423 | AAATTATAAAGTGAG[A/C]TAACGAAGAATGAGA | 216080 |
rs29941311 | snp | C/T | 0.277778 | 0.248452 | utr-variant-3-prime | Ube2d1 | GRCm38.p3 | 10:71255513 | GTGAAAAACGTCTCG[C/T]TTCAGAGAAAGAAAA | 216080 |
rs29941313 | snp | C/T | 0.336735 | 0.234472 | utr-variant-3-prime | Ube2d1 | GRCm38.p3 | 10:71255544 | GCGTCTGGTTGCTTT[C/T]TCAGTCACGTCACAG | 216080 |
rs29942135 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2d1 | Mm_Celera | 10:71267705 | GCAATGGGTAGAACA[C/T]CAGCCAGACCATGAC | 216080 |
rs29942137 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2d1 | Mm_Celera | 10:71268067 | GTGAAATCCTAACAG[C/T]CATAGAAAAGAATAG | 216080 |
rs29942139 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ube2d1 | Mm_Celera | 10:71268080 | AGTCATAGAAAAGAA[C/T]AGCACAGATCCCACA | 216080 |
rs29942141 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2d1 | Mm_Celera | 10:71268185 | AGTATTTACTACAGT[C/T]TCTGCTATTACAATA | 216080 |
rs29942143 | snp | C/G | 0.32 | 0.24 | intron-variant | Ube2d1 | Mm_Celera | 10:71268629 | ACCGGGCAAGCAAAT[C/G]CAGTGTTAAGATCCC | 216080 |
rs29942215 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Ube2d1 | Mm_Celera | 10:71255745 | TGGAACGAAGGACAC[A/G]GCAAACGGCGCCCGG | 216080 |
rs29942217 | snp | A/C | 0.336735 | 0.234472 | utr-variant-3-prime | Ube2d1 | GRCm38.p3 | 10:71255765 | ACGGCGCCCGGCTTA[A/C]TGCTAACGCTGGAAA | 216080 |
rs29942219 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Ube2d1 | GRCm38.p3 | 10:71255807 | TTACAGTACTCTGGC[A/G]TAAGTGAAAGTGTTT | 216080 |
rs29942221 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Ube2d1 | Mm_Celera | 10:71255862 | AGTCCATTCTCTTGC[A/G]TGCCTGTTGTATCTG | 216080 |
rs29942223 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2d1 | Mm_Celera | 10:71256731 | GGAGAGAGAACATTC[C/T]GTTAGGCGCTGCCAC | 216080 |
rs29943135 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ube2d1 | Mm_Celera | 10:71256790 | AAAAGGCTGAGCATG[A/G]CCGTACTGGGCGTAA | 216080 |
rs29943137 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2d1 | Mm_Celera | 10:71256861 | GTGGCTCAGTGACAG[A/G]TGGCTTGAGAAGCCC | 216080 |
rs29943139 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2d1 | Mm_Celera | 10:71257155 | GGAACGAGTCTGAAG[C/T]CATTTGCATCCTCAG | 216080 |
rs29943141 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2d1 | Mm_Celera | 10:71257946 | GCCTTTAGTTCCTGA[A/G]TTTTAAATCTCTGGT | 216080 |
rs29943143 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2d1 | Mm_Celera | 10:71257952 | AGTTCCTGAATTTTA[A/G]ATCTCTGGTTTCATT | 216080 |
rs29943145 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2d1 | Mm_Celera | 10:71268739 | CATGAAGTAGCTGCA[C/T]TGTGGTTTACATAAG | 216080 |
rs29943147 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2d1 | Mm_Celera | 10:71269312 | TAGAGTTGGGCACCT[A/G]TAATAGATTCTTAAT | 216080 |
rs29943149 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2d1 | Mm_Celera | 10:71269380 | TTTCATTTTTACTTA[C/T]ATTCCAAGAGAGGGT | 216080 |
rs29943151 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2d1 | Mm_Celera | 10:71269620 | GTATGATTCAAGTCA[C/T]GTTCCCGTCAAATTT | 216080 |
rs29943153 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2d1 | Mm_Celera | 10:71269799 | CATCACTGAACATCA[C/T]GGCATTTGAAAATGA | 216080 |
rs29944065 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2d1 | Mm_Celera | 10:71270269 | CAATTCAGGTTATGT[C/T]ATTTTGTCTTAGAAT | 216080 |
rs29944067 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Ube2d1 | Mm_Celera | 10:71274532 | ACAGAGGCAAGTCTC[C/T]ACTGTCATTTCTGCT | 216080 |
rs29944069 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ube2d1 | Mm_Celera | 10:71274537 | GGCAAGTCTCTACTG[C/T]CATTTCTGCTTATAC | 216080 |
rs29944071 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ube2d1 | Mm_Celera | 10:71275631 | CGAAGCTGGCCTGGG[C/T]TACACAGTAACTTGA | 216080 |
rs29944073 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2d1 | Mm_Celera | 10:71276209 | TAGAGAATGACATTA[C/T]ATCCTCCTCAACCAG | 216080 |
rs29944085 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ube2d1 | Mm_Celera | 10:71258185 | GCCTATTTTTAAATC[C/T]GAAAAACAAAATTAC | 216080 |
rs29944087 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2d1 | Mm_Celera | 10:71258334 | TGGAACAAAAAGGGT[A/G]TTGGTTGCCACAAAT | 216080 |
rs29944089 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2d1 | Mm_Celera | 10:71258354 | TTGCCACAAATAGGA[A/G]CAAACAGAACCGATC | 216080 |
rs29944091 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2d1 | Mm_Celera | 10:71258427 | CAGACTTGTATACGC[A/G]CAGCTCAGCCCCTGG | 216080 |
rs29944093 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ube2d1 | Mm_Celera | 10:71258673 | ATCTGTCAGGGCGGA[A/C]GTGGGATGCCTCAGC | 216080 |
rs29944875 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2d1 | Mm_Celera | 10:71258723 | AACCACAGAGAAGCC[A/G]GGTCTTGACAGAGCC | 216080 |
rs29944877 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2d1 | Mm_Celera | 10:71258758 | TTGTGTGACGTCATC[A/C]GTATGATTTTTAAGC | 216080 |
rs29944879 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ube2d1 | Mm_Celera | 10:71258764 | GACGTCATCCGTATG[A/T]TTTTTAAGCTGGGTG | 216080 |
rs29944881 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ube2d1 | Mm_Celera | 10:71258780 | TTTTTAAGCTGGGTG[G/T]TTTTTAAAGTGCTAT | 216080 |
rs29944883 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2d1 | Mm_Celera | 10:71259321 | CTGTAAAAACATTCC[A/G]AACAACTCATATCTC | 216080 |
rs29944975 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ube2d1 | Mm_Celera | 10:71276730 | GCTACATTAGGCAGC[G/T]CTCTCCAATTACCTG | 216080 |
rs29944977 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2d1 | Mm_Celera | 10:71276770 | ATTACCCTTAAAGGA[C/T]CAGGACACGTGTCAA | 216080 |
rs29944979 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ube2d1 | Mm_Celera | 10:71276878 | ATAATTGATCTCAAA[C/T]CAGAGGACCCACTAA | 216080 |
rs29944981 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2d1 | Mm_Celera | 10:71276960 | AACATCAGAATTTAT[C/T]TCACGTGGCTGGAGA | 216080 |
rs29944983 | snp | C/T | 0.124444 | 0.216185 | intron-variant, missense | Ube2d1 | Mm_Celera | 10:71277399 | AAGTGGTGTACTCTG[C/T]TCTTCATGATACCCA | 216080 |
rs29945695 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2d1 | Mm_Celera | 10:71259366 | CCCAGGAGCCTAGCA[A/G]GCATAGGAAAACAGC | 216080 |
rs29945697 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Ube2d1 | Mm_Celera | 10:71259955 | CAGCTTGTAAAAAAA[A/C]CCCACGATTCTTGCA | 216080 |
rs29945699 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ube2d1 | Mm_Celera | 10:71260216 | AAGTTCTAATGTCTA[A/C]ACAGGTACAACCAAA | 216080 |
rs29945701 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2d1 | Mm_Celera | 10:71260345 | TAAAACCAAGCTGGA[C/T]GAATTCAGTGTTCAT | 216080 |
rs29945703 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2d1 | Mm_Celera | 10:71261145 | CCTGAGATGTGCCTC[C/T]GTGCCACAGCTCTGA | 216080 |
rs47335455 | snp | G/T | | | intron-variant | Ube2d1 | Mm_Celera | 10:71283180 | TCAGCTGGTGGGGGG[G/T]GGGGGGGAAGGGGTG | 216080 |
rs211775260 | in-del | -/T | | | intron-variant | Ube2d1 | Mm_Celera | 10:71263563 | AAATAAATAAATAAA[-/T]AAAAGACTTGAGTTC | 216080 |
rs211795860 | snp | A/G | | | intron-variant | Ube2d1 | Mm_Celera | 10:71275336 | AGCCAAGCAAAGGTC[A/G]GGAAGGGTTGGGTCA | 216080 |
rs211815442 | snp | C/T | | | intron-variant | Ube2d1 | Mm_Celera | 10:71267168 | AAAACGACTTAGTGA[C/T]GTAACAAGATGGCCA | 216080 |
rs211846911 | snp | C/T | | | intron-variant | Ube2d1 | Mm_Celera | 10:71265905 | CAGGTGGTTGTGAGC[C/T]ACCATGTGGTTGTTG | 216080 |
rs211855755 | snp | C/T | | | intron-variant | Ube2d1 | Mm_Celera | 10:71266487 | AACTCCCTTACAATC[C/T]GAGCGCGTGGTACTT | 216080 |
rs211858309 | in-del | -/TGTGTGTA | | | intron-variant | Ube2d1 | Mm_Celera | 10:71268951 | ATTTGTGTGTGTGTG[-/TGTGTGTA]TGTGTATGGGGGGAC | 216080 |
rs211910468 | snp | A/C | | | intron-variant | Ube2d1 | Mm_Celera | 10:71283405 | GAAAGAAGATGTGGA[A/C]ATTTGCCATATTAAC | 216080 |
rs211946797 | snp | A/C | | | intron-variant | Ube2d1 | Mm_Celera | 10:71284822 | GAAGGCCGCCCGTTG[A/C]AGAGCAAGCCCCGGC | 216080 |
rs211980492 | snp | A/G | | | intron-variant | Ube2d1 | Mm_Celera | 10:71274533 | CAGAGGCAAGTCTCT[A/G]CTGTCATTTCTGCTT | 216080 |
rs212131061 | in-del | -/ACACACACACACACACACAC | | | intron-variant | Ube2d1 | Mm_Celera | 10:71267907 | AACTCCTACAAATCA[-/ACACACACACACACACACAC]ACACACACACACACA | 216080 |
rs212192540 | snp | A/G | | | intron-variant | Ube2d1 | Mm_Celera | 10:71258033 | TTACTGAAAACCAGC[A/G]TGACTAAAGAGTTCT | 216080 |
rs212328985 | snp | A/G | | | intron-variant | Ube2d1 | Mm_Celera | 10:71265060 | TGCTTTCCAGGTTTC[A/G]ATTTTCTTTTGTACA | 216080 |
rs212362711 | in-del | -/GGGGGGGGGG | | | intron-variant | Ube2d1 | Mm_Celera | 10:71263774 | AATGTAGCTGGGGGC[-/GGGGGGGGGG]GGGGGGGGGGGAGGG | 216080 |
rs212388479 | snp | A/G | | | intron-variant | Ube2d1 | Mm_Celera | 10:71257525 | ATGCTGGGATTTAAA[A/G]GTATACACCACCCCT | 216080 |
rs212464316 | snp | G/T | | | intron-variant | Ube2d1 | Mm_Celera | 10:71273379 | GGGAAGGGCAAGCCA[G/T]AGTGGCCTTATTTTC | 216080 |
rs212525926 | snp | A/G | | | intron-variant | Ube2d1 | Mm_Celera | 10:71280223 | TTATATCTCCTCAGA[A/G]AAGGAGTTTCAGAAC | 216080 |
rs212589362 | snp | A/G | | | intron-variant | Ube2d1 | Mm_Celera | 10:71280985 | GGATGTGTGCATACC[A/G]GGTGAGCACTTTGCC | 216080 |
rs212744934 | snp | C/T | | | intron-variant | Ube2d1 | Mm_Celera | 10:71263959 | GCGGGAAGGGTGAGA[C/T]GAGCCTGGGAAGATA | 216080 |
rs212796974 | snp | C/T | | | intron-variant | Ube2d1 | Mm_Celera | 10:71263113 | TACAATATTGATTCA[C/T]GACTTTTTCTAGCCT | 216080 |