SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs30459680 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134960722 | CTCCTGGCCAACTAG[A/G]GCTGCATCGTGAGAC | 67196 |
rs30702543 | snp | C/G | 0.5 | 0 | intron-variant | Ube2t | GRCm38.p3 | 1:134965400 | TCCATTATCCTGATG[C/G]CATCATCATGCAGGC | 67196 |
rs30709527 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2t | GRCm38.p3 | 1:134965494 | TTCTGCAGGTAGCCA[A/G]GAGGAGACTGGAATT | 67196 |
rs30833484 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134962081 | GACCGTGCTCGGCTA[A/G]CTTGTATCTTTAGAC | 67196 |
rs30833485 | snp | C/G | 0.426035 | 0.177515 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134962063 | ATTTCAACATGCCTG[C/G]GCGACCGTGCTCGGC | 67196 |
rs30833486 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134962022 | AATCTATGTACCCAA[A/G]GCTGGTCTCAAATTC | 67196 |
rs30833487 | snp | C/G | 0.459184 | 0.136902 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134961876 | AACCCCTAACAGGTT[C/G]AAGCTTCCATATGAA | 67196 |
rs30833488 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Ube2t | Mm_Celera | 1:134961857 | GCAGAGGATCTCTTG[C/T]GTTAACCCCTAACAG | 67196 |
rs30833489 | snp | A/G | 0.473373 | 0.11227 | upstream-variant-2KB | Ube2t | Mm_Celera | 1:134961790 | CAGTATGTAGGAAGA[A/G]CGGGCTTGTTTTCAG | 67196 |
rs30833490 | snp | C/T | 0.391111 | 0.206368 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134961734 | TTGAAAGTCATTTAT[C/T]CCGTGGTTGGTGTGT | 67196 |
rs30833491 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Ube2t | Mm_Celera | 1:134961587 | GTTCTGCTGAGTCTC[A/G]GGTCTTAAGCTTTCC | 67196 |
rs30833492 | snp | C/G | 0.459184 | 0.136902 | upstream-variant-2KB | Ube2t | Mm_Celera | 1:134961517 | AAGAGAAAGGTGATT[C/G]CTTGATTGATTTCTG | 67196 |
rs30833493 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Ube2t | Mm_Celera | 1:134961461 | AAAGACCGACTGCTA[A/G]GTCTATGCTATGGAG | 67196 |
rs30834504 | snp | C/T | 0.459184 | 0.136902 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134961257 | CTATCTACCCTCTGG[C/T]TCAGTCCTACAACTA | 67196 |
rs30834505 | snp | C/T | 0.290657 | 0.246672 | upstream-variant-2KB | Ube2t | Mm_Celera | 1:134961175 | ACAGAACCGCAACAG[C/T]AGACTGAAAAGCACG | 67196 |
rs30834506 | snp | A/G/T | 0.492188 | 0.0620098 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134961168 | CATGAATACAGAACC[A/G/T]CAACAGTAGACTGAA | 67196 |
rs30834507 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134961106 | AAAATAAGCAGTAAT[C/T]CCAAATGGTAAGCGA | 67196 |
rs30834508 | snp | A/G | 0.493827 | 0.0552116 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134961034 | CACTGTCGGAGTAGG[A/G]ACAAGAAAAGATGCT | 67196 |
rs30834509 | snp | G/T | 0.391111 | 0.206368 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134961022 | GACTAATACGGTCAC[G/T]GTCGGAGTAGGGACA | 67196 |
rs30834510 | snp | C/G | 0.459184 | 0.136902 | upstream-variant-2KB | Ube2t | Mm_Celera | 1:134960962 | GACATTTTTAACTCT[C/G]TGTTTTTCAAAGAAC | 67196 |
rs30834511 | snp | A/T | 0.391111 | 0.206368 | upstream-variant-2KB | Ube2t | Mm_Celera | 1:134960923 | CTTTGATCCAACTCA[A/T]TACGGTCTGTGCTAT | 67196 |
rs30834512 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Ube2t | Mm_Celera | 1:134960807 | TAGAGCACTCTTGTT[A/G]GCCTCTATTCCCACC | 67196 |
rs30837575 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ube2t | GRCm38.p3 | 1:134970908 | CTGGCTATTTCAACT[C/T]TTTGATTGCTAGTAA | 67196 |
rs30837576 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Ube2t | GRCm38.p3 | 1:134970612 | ATTCTTTTTAAAAAC[A/G]TTTCAAAGATATAAT | 67196 |
rs30837577 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ube2t | Mm_Celera | 1:134970595 | GCCTGGCGCAACAAG[A/G]GATTCTTTTTAAAAA | 67196 |
rs30837578 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Ube2t | Mm_Celera | 1:134970587 | GCCCCCAAGCCTGGC[A/G]CAACAAGGGATTCTT | 67196 |
rs30837579 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2t | GRCm38.p3 | 1:134970168 | CAATGTGTAAGTCTA[A/G]TTGGAGCCTGTTTGA | 67196 |
rs30837580 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ube2t | Mm_Celera | 1:134970157 | GTAACTAAATCCAAT[A/G]TGTAAGTCTAATTGG | 67196 |
rs30837581 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ube2t | GRCm38.p3 | 1:134970143 | ACTGAAGAGATATGG[C/T]AACTAAATCCAATGT | 67196 |
rs30837582 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2t | Mm_Celera | 1:134970123 | CTTTGCAAGGTTTGT[C/T]TGTCACTGAAGAGAT | 67196 |
rs30837583 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2t | GRCm38.p3 | 1:134970117 | CTGGAGCTTTGCAAG[A/G]TTTGTTTGTCACTGA | 67196 |
rs30838474 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2t | GRCm38.p3 | 1:134970061 | TTGTTAAACCTGAAT[A/G]AGTAGCTTAATAATT | 67196 |
rs30838475 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Ube2t | GRCm38.p3 | 1:134970011 | TTAACTATTAAAACT[A/G]GACATTTCTGTACCA | 67196 |
rs30838476 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2t | GRCm38.p3 | 1:134969943 | TCAGTCAAGTGTCTC[A/G]TAAGGCTCCAGTCAG | 67196 |
rs30838477 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2t | Mm_Celera | 1:134969942 | TTCAGTCAAGTGTCT[C/T]GTAAGGCTCCAGTCA | 67196 |
rs30838478 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Ube2t | GRCm38.p3 | 1:134969367 | CATTGAAAGACAGAC[A/C]GTATACTATTTAGAG | 67196 |
rs30838479 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Ube2t | GRCm38.p3 | 1:134969355 | GTAAGGCACAGCCAT[C/T]GAAAGACAGACAGTA | 67196 |
rs30838480 | snp | C/T | 0.408163 | 0.193609 | synonymous-codon | Ube2t | GRCm38.p3 | 1:134969257 | AATACTAGGTGGAGC[C/T]AATACACCTTATGAG | 67196 |
rs30838481 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ube2t | GRCm38.p3 | 1:134968700 | TTACACCCACTTCCT[C/T]TTTTCCCCTTTCGTT | 67196 |
rs30838482 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Ube2t | GRCm38.p3 | 1:134968683 | TTAACAGAATTGCTG[A/T]CTTACACCCACTTCC | 67196 |
rs30838483 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ube2t | Mm_Celera | 1:134968649 | ACAAGAAACACTGCA[A/T]GGAGACACAGTTAAA | 67196 |
rs30839034 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2t | Mm_Celera | 1:134967958 | GATATTAAAGTAGTG[C/T]GTAGTAAGGTGAAAG | 67196 |
rs30839035 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2t | GRCm38.p3 | 1:134967917 | GGTAGCCCTATCGAA[A/G]ACTGTCCTAATTTCA | 67196 |
rs30839036 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon | Ube2t | Mm_Celera | 1:134967858 | TCCCCCGGGCATCAC[A/G]TGCTGGCAGGAAAAG | 67196 |
rs30839037 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Ube2t | GRCm38.p3 | 1:134967849 | CATCGAACCTCCCCC[A/G]GGCATCACGTGCTGG | 67196 |
rs30839038 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2t | Mm_Celera | 1:134967681 | AAGCTGTGCTAAAAA[C/T]GCTAGTCAGCATGGC | 67196 |
rs30839039 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ube2t | Mm_Celera | 1:134967637 | CCTTTGTCACAGAGA[G/T]TAATAAGAATCTGTT | 67196 |
rs30839040 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2t | Mm_Celera | 1:134967570 | AAACTTTTACAGTTA[C/T]TATTTGTATGAGTAG | 67196 |
rs30839041 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ube2t | Mm_Celera | 1:134967197 | TAGGATTCTATAGAC[G/T]GCTGCTGGTTGAGTG | 67196 |
rs30839042 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2t | GRCm38.p3 | 1:134967128 | ATGTGTTCATCTAAA[C/T]TGTAGCAAAGTAAGC | 67196 |
rs30839043 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Ube2t | GRCm38.p3 | 1:134967110 | CTGCAAAAAGAAAGG[A/G]AGATGTGTTCATCTA | 67196 |
rs30839934 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Ube2t | GRCm38.p3 | 1:134967077 | GGTAAAACTTATGAA[C/T]GAGGCTCTCAGCCAG | 67196 |
rs30839935 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Ube2t | Mm_Celera | 1:134966882 | TAAAGAATATGTAGG[A/T]AAACAACTTTAAATG | 67196 |
rs30839936 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Ube2t | GRCm38.p3 | 1:134966232 | ATAATATGTGCAATA[C/T]CACCTAGTGACTGGT | 67196 |
rs30839937 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ube2t | Mm_Celera | 1:134965136 | TGAGGCAGAAGAATA[C/T]GGGACCGGATTTGGG | 67196 |
rs30839938 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Ube2t | GRCm38.p3 | 1:134964909 | CTTTTTATGTGGTTT[C/T]TGAATTAAACTCAGG | 67196 |
rs30839939 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Ube2t | Mm_Celera | 1:134964686 | TATTATAGCTCTCTC[C/T]GGCCTCACTCTCTCC | 67196 |
rs30839940 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2t | Mm_Celera | 1:134964646 | GCACCTTCTCACACC[A/G]CTTTTTTATTTTAAT | 67196 |
rs30839941 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2t | GRCm38.p3 | 1:134963480 | TAAAGATACAGTTTA[C/T]AGTTGTAGGTAGTTT | 67196 |
rs30839942 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ube2t | GRCm38.p3 | 1:134963449 | GCATGCCTTTCCACT[A/G]TGTTCTTATTTTATA | 67196 |
rs30839943 | snp | C/G | 0.486111 | 0.0821678 | intron-variant | Ube2t | GRCm38.p3 | 1:134963133 | ACATGATAACACATG[C/G]CTTTTATACCAAAGG | 67196 |
rs30840644 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Ube2t | Mm_Celera | 1:134963118 | TTATATTCATAAAAT[A/G]CATGATAACACATGG | 67196 |
rs30840645 | snp | A/G/T | 0.625 | 0.125 | intron-variant | Ube2t | Mm_Celera | 1:134962946 | GGAAAATATCTTTTG[A/G/T]AGCCGTAGTGTAAGG | 67196 |
rs30840646 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Ube2t | Mm_Celera | 1:134962942 | AAAAGGAAAATATCT[A/T]TTGAAGCCGTAGTGT | 67196 |
rs30840647 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ube2t | Mm_Celera | 1:134962884 | ACGTTTGCGGGGAGT[G/T]GTTACTGGAAAAGAG | 67196 |
rs30840648 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2t | Mm_Celera | 1:134962825 | TACCTCAGGCCTGGG[A/G]CACAAAGAATTTTAC | 67196 |
rs30840649 | snp | G/T | 0.5 | 0 | intron-variant | Ube2t | GRCm38.p3 | 1:134962801 | GGTTCTGTGCATTGA[G/T]TATTTATTTACCTCA | 67196 |
rs30840650 | snp | C/T | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Ube2t | GRCm38.p3 | 1:134962778 | CTCCAGCATCTGCCA[C/T]CTACCCAGGTTCTGT | 67196 |
rs30840651 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Ube2t | Mm_Celera | 1:134962709 | TTTCTACCCGAGCGG[C/T]CCTGGGAGGAACACG | 67196 |
rs30840652 | snp | A/C | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Ube2t | Mm_Celera | 1:134962691 | TCTGGGGAAGGAGTC[A/C]CGTTTCTACCCGAGC | 67196 |
rs30840653 | snp | A/C | 0.444444 | 0.157135 | utr-variant-5-prime | Ube2t | GRCm38.p3 | 1:134962601 | TGAGCACAGCAGAGG[A/C]GCGCCGCGGTAAGTG | 67196 |
rs30841394 | snp | C/G | 0.459184 | 0.136902 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134962481 | CGCAAGCTCTGAGCG[C/G]TGGCCAATAGGCGGG | 67196 |
rs30841395 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2t | Mm_Celera | 1:134962454 | CGCCAATTTGAGCGG[C/T]GCGTGAGCGGACGCA | 67196 |
rs30841396 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134962416 | CCACAGCGGGAACTG[A/G]GAATTCCGGATACGC | 67196 |
rs30841397 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134962384 | CTTCCCAGCTCACAG[C/T]CGATTTACAAACAAG | 67196 |
rs30841398 | snp | A/G | 0.459184 | 0.136902 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134962356 | TTTCCTCTCCTGTAG[A/G]TGACTTCCCAGCCTT | 67196 |
rs30841399 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134962304 | AGCTACTCAGCAGTC[A/G]CTTCTCCAGATTAAG | 67196 |
rs30841400 | snp | A/T | 0.408163 | 0.193609 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134962132 | GTAAAGTTTCCCCTG[A/T]CATTGCTTAAAGCCT | 67196 |
rs30841401 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134962089 | TCGGCTAACTTGTAT[C/T]TTTAGACTACTGATC | 67196 |
rs31258834 | snp | C/T | | | intron-variant | Ube2t | GRCm38.p3 | 1:134969832 | AGAACTTTTTCATCC[C/T]CCCAAACTGTAACTT | 67196 |
rs31334920 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2t | Mm_Celera | 1:134963132 | TACATGATAACACAT[A/G]GCTTTTATACCAAAG | 67196 |
rs31374405 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2t | GRCm38.p3 | 1:134966175 | TTCCTGCCTCAGCCT[C/T]CCAATTGATGAGATT | 67196 |
rs31378343 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2t | Mm_Celera | 1:134963821 | TCTTCCTTCAGCAGT[A/G]TACTGTGATGTAGAA | 67196 |
rs31430457 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2t | GRCm38.p3 | 1:134965712 | AGTATAGGCTATAGA[A/G]TCATCTAGGAGACAG | 67196 |
rs31438801 | snp | A/C | 0.32 | 0.24 | intron-variant | Ube2t | GRCm38.p3 | 1:134965683 | AGGGTGAGATGGTTA[A/C]TATTGTCAACTGAAG | 67196 |
rs31506717 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Ube2t | GRCm38.p3 | 1:134963054 | AACTGACTTCTACCT[A/C/T]GGCGCCTCCAGTGTC | 67196 |
rs31519427 | snp | C/T | 0.5 | 0 | intron-variant | Ube2t | GRCm38.p3 | 1:134973762 | TACTTTTTCCATTGA[C/T]GATGTAGATGTTGTG | 67196 |
rs31569973 | snp | C/T | 0.5 | 0 | downstream-variant-500B | Ube2t | GRCm38.p3 | 1:134974381 | TTGCCAGTGCTTTCA[C/T]TCTGGGATTTATGTA | 67196 |
rs31744931 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2t | GRCm38.p3 | 1:134960732 | ACTAGAGCTGCATCG[C/T]GAGACCCTGTCTCAA | 67196 |
rs31782126 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ube2t | GRCm38.p3 | 1:134966035 | ACAGAGGAACACCAC[A/C]CTGTGGCCCAGGCTG | 67196 |
rs31937135 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ube2t | Mm_Celera | 1:134973711 | TGCCCACTAAAATCT[A/T]AAAACAAAGAATATC | 67196 |
rs31959425 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2t | GRCm38.p3 | 1:134966060 | AGGCTGACCTCAGAC[C/T]TAGAGTAATCCTCCT | 67196 |
rs31971167 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2t | GRCm38.p3 | 1:134966345 | AGTTATATCCCCAGC[C/T]CCTGAACTGAAGACA | 67196 |
rs31993637 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2t | Mm_Celera | 1:134970572 | GATTAAAGGCGTGGT[A/G]CACGCCCAAGCCTGG | 67196 |
rs32030554 | snp | A/G | 0.5 | 0 | intron-variant | Ube2t | Mm_Celera | 1:134973611 | GAGTGTGTCACTACC[A/G]CCCGACACCTTTTGA | 67196 |
rs32161704 | snp | A/C | 0.5 | 0 | intron-variant | Ube2t | GRCm38.p3 | 1:134971713 | AGGCAAACAAAAAGT[A/C]CTTAGGTTACATACA | 67196 |
rs32274160 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2t | GRCm38.p3 | 1:134964024 | TCCAGGACAACTAGG[A/G]CTACAAAAAGAAACC | 67196 |
rs32306693 | snp | G/T | 0.375 | 0.216506 | downstream-variant-500B | Ube2t | GRCm38.p3 | 1:134974196 | CGTGTGTCTGGGAGT[G/T]AACTGCTTATAGTGC | 67196 |
rs32317769 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2t | Mm_Celera | 1:134970586 | CACGCCCAAGCCTGG[C/T]GCAACAAGAGATTCT | 67196 |
rs32322246 | snp | A/T | 0.32 | 0.24 | intron-variant | Ube2t | GRCm38.p3 | 1:134965709 | TGAAGTATAGGCTAT[A/T]GAGTCATCTAGGAGA | 67196 |