SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4229242 | snp | C/G | 0.408163 | 0.193609 | utr-variant-3-prime | Ube2f | Mm_Celera | 1:91285503 | TGTCCTGAAGAAGAC[C/G]CTCCTGACTGCCCAC | 67921 |
rs13470238 | snp | A/T | | | utr-variant-3-prime | Ube2f | Mm_Celera | 1:91285750 | ACTGGCAGATTGGCA[A/T]TAAGAAACCCGCTAT | 67921 |
rs13470239 | snp | A/G | | | utr-variant-3-prime | Ube2f | Mm_Celera | 1:91285570 | TGTCTGGGCCTCAAG[A/G]GAGTTGTCTGCTTCC | 67921 |
rs30461852 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2f | GRCm38.p3 | 1:91255296 | GGTTGAAGGCAGTGG[A/G]TTTGTGCAGATTTAA | 67921 |
rs30493989 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2f | GRCm38.p3 | 1:91259889 | GTGGTTGTTCCTTTA[C/T]AGCAGTGCTCTTCCA | 67921 |
rs30668539 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2f | Mm_Celera | 1:91264293 | TATATATATATATGT[A/G]TGTGTGTGTATATAT | 67921 |
rs30705431 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Ube2f | Mm_Celera | 1:91263590 | ATGCTTTGGAAGTCC[A/G]TGTGAGTGGTGTGAC | 67921 |
rs30716262 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2f | Mm_Celera | 1:91259055 | ATATTTTTATTGTAG[C/T]AGGCCACACAGAACA | 67921 |
rs30794138 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2f | GRCm38.p3 | 1:91254958 | TGTTTCATGTGGGAC[A/G]TAGCCTAAGGAAAAA | 67921 |
rs30819899 | snp | A/C | 0.5 | 0 | intron-variant | Ube2f | GRCm38.p3 | 1:91252113 | AGCCCGTGGGCAGCC[A/C]TGGCAGGTCTGAGCA | 67921 |
rs30843539 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Ube2f | Mm_Celera | 1:91272295 | AGTAAAATGTTTTTA[A/C]CTTAAGCAACTGTGG | 67921 |
rs30891988 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2f | Mm_Celera | 1:91253201 | TGAGAAACTAGACAG[A/C]AGAGTTGCATTTGAG | 67921 |
rs30901205 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ube2f | GRCm38.p3 | 1:91277131 | CTTCTCATATTCATA[C/T]AATGTGCTGGGACCT | 67921 |
rs31013050 | snp | A/G | 0.5 | 0 | intron-variant | Ube2f | GRCm38.p3 | 1:91252488 | TGTTCTGCTGTTTTG[A/G]TAGCTTGTGGGCTGA | 67921 |
rs31013802 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2f | Mm_Celera | 1:91277080 | TGGACAGGCTATCAC[A/G]GCACTGCCTCATGTT | 67921 |
rs31080638 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ube2f | GRCm38.p3 | 1:91278687 | TACTGTCAGAATATG[C/G]AGACTCATGCAGTTG | 67921 |
rs31092997 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Ube2f | GRCm38.p3 | 1:91280374 | GCAGGTCAGCTGTAG[C/T]CTCTGTGCTGAGCTT | 67921 |
rs31105059 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2f | GRCm38.p3 | 1:91277879 | CTTTTCTGGTGGGTG[C/T]GATGACACATACCTG | 67921 |
rs31138821 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2f | GRCm38.p3 | 1:91277841 | GCTTTTAGTCAACAC[A/G]TGTGTATACTGTTTT | 67921 |
rs31139299 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2f | Mm_Celera | 1:91249733 | AACCCCAAGGCCTCA[C/G]GAGGTAGGGTCTCTC | 67921 |
rs31150184 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2f | GRCm38.p3 | 1:91253250 | CTGAAGAGAGGAATA[G/T]TCTTGTGTTCATGGT | 67921 |
rs31191214 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2f | Mm_Celera | 1:91275734 | TAGATCAGTAGGGAA[A/G]TAAGGTGATATATAG | 67921 |
rs31238296 | snp | G/T | 0.32 | 0.24 | intron-variant | Ube2f | GRCm38.p3 | 1:91265607 | CAGGAGGAGAGTCAT[G/T]AATCCTGTCTTAGAC | 67921 |
rs31287666 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Ube2f | GRCm38.p3 | 1:91284522 | TGCATCAGAGATACT[A/G]TATGTCCTTAGTTTG | 67921 |
rs31309918 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2f | GRCm38.p3 | 1:91280184 | GCCTTAGCCCACTAT[A/G]TAGTCCAGGGAATCC | 67921 |
rs31331215 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ube2f | GRCm38.p3 | 1:91266411 | AACTAATTAAGTGAG[C/T]GGTACAGAATTTTGT | 67921 |
rs31335024 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2f | Mm_Celera | 1:91255881 | TTCCAGGGGATCCAA[C/T]ACCCTCATGAAGATG | 67921 |
rs31424152 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2f | Mm_Celera | 1:91282367 | AAAGTTCCATAACAT[C/T]TGTTTCTCAATACTT | 67921 |
rs31426156 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ube2f | GRCm38.p3 | 1:91251273 | ACACTCATGCTGTAC[G/T]GTTTAAGTCCCGATC | 67921 |
rs31444024 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ube2f | Mm_Celera | 1:91252102 | AGCATTAAGAGAGCC[C/G]GTGGGCAGCCATGGC | 67921 |
rs31483771 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2f | GRCm38.p3 | 1:91283443 | GTCTCAACTACCCCA[C/T]CCTCCAAAGAATGGT | 67921 |
rs31525113 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ube2f | GRCm38.p3 | 1:91282326 | GATATAACTCCCCCC[A/T]TTTTATTTTATGACA | 67921 |
rs31546123 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2f | Mm_Celera | 1:91281232 | GTTGGGTCTTAATTG[C/T]ATCTATTTGTCCCTA | 67921 |
rs31546218 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2f | Mm_Celera | 1:91268135 | AAGAACAGATTTTTT[C/T]CCCCTTAGTGAGTCT | 67921 |
rs31595018 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Ube2f | Mm_Celera | 1:91248705 | TGGCTATTCCTGGTT[A/G]TCAACTTGACTATAT | 67921 |
rs31602197 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2f | GRCm38.p3 | 1:91263470 | GCTCAGGAGGTGGCT[C/T]GGTAGCAGAGTACTT | 67921 |
rs31643505 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ube2f | Mm_Celera | 1:91279409 | TTGTCTTGAGGAAAA[C/T]ATATTTTGATAGCCT | 67921 |
rs31719851 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2f | Mm_Celera | 1:91283872 | GAAGCTCTTGTCAGC[A/G]CCGGGGCACTAAGAC | 67921 |
rs31731706 | snp | A/G | 0.5 | 0 | intron-variant | Ube2f | Mm_Celera | 1:91257463 | GTGTCTCCCACGCTA[A/G]GCCGACTTGCCACAC | 67921 |
rs31761462 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Ube2f | GRCm38.p3 | 1:91272808 | GCAGTGCAGAGTCAG[C/T]CAGCAAAATACAGTG | 67921 |
rs31766527 | snp | C/T | 0.255 | 0.24995 | intron-variant | Ube2f | GRCm38.p3 | 1:91265724 | CAAGTGCCTAGTCTA[C/T]AGGGGCAGCAGCATC | 67921 |
rs31808778 | snp | A/G/T | 0.56 | 0.195959 | intron-variant | Ube2f | GRCm38.p3 | 1:91272828 | AAAATACAGTGTGGC[A/G/T]GGAGGGGTGGCTGCA | 67921 |
rs31821538 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2f | Mm_Celera | 1:91251306 | TTTCTTTCAACTTGG[A/G]AGGTTAAACGGCCCT | 67921 |
rs31887465 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Ube2f | GRCm38.p3 | 1:91280726 | CCGAGTCAATTATGG[A/G]AACTGAAGCAAGATG | 67921 |
rs31888729 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2f | Mm_Celera | 1:91264265 | TATATATATGTTTGT[A/G]TATATATATGTATAT | 67921 |
rs31911607 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2f | Mm_Celera | 1:91251415 | TGCATAGGTCACACC[A/G]GCCTGATTTCAGCAC | 67921 |
rs31921327 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2f | GRCm38.p3 | 1:91252040 | AGTAGAGCAGGGTAC[A/G]CCCATCCTCTGCCTC | 67921 |
rs32027113 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2f | Mm_Celera | 1:91283332 | CACCCTAATTCTAGC[A/G]CTTGGGATGCAGAGA | 67921 |
rs32033171 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ube2f | Mm_Celera | 1:91254446 | ACAAATGAAGCTTGT[C/G]TGGAGGCTCCTTGGG | 67921 |
rs32035047 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2f | Mm_Celera | 1:91283875 | GCTCTTGTCAGCGCC[A/G]GGGCACTAAGACTTT | 67921 |
rs32054259 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2f | Mm_Celera | 1:91269166 | AGAAAAAGGGGAAAT[A/G]AGCAGTTAAGAGGAT | 67921 |
rs32059437 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ube2f | Mm_Celera | 1:91262352 | TGACATGAAGAAAAC[C/T]CATTTTGTTCTAATA | 67921 |
rs32087327 | snp | A/G | 0.5 | 0 | intron-variant | Ube2f | GRCm38.p3 | 1:91281633 | AACACATGCACTAAC[A/G]TTTGTTTGAAATCCA | 67921 |
rs32091928 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2f | Mm_Celera | 1:91252655 | TCAGTGTTCGTATAG[A/G]CTACGCCATGACCAT | 67921 |
rs32096789 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2f | Mm_Celera | 1:91264291 | TATATATATATATAT[A/G]TGTGTGTGTGTATAT | 67921 |
rs32210654 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Ube2f | GRCm38.p3 | 1:91272939 | TGCAGAGTGAAAAAA[A/C/T]CTGACATAAAAATCC | 67921 |
rs32219550 | snp | A/C | 0.5 | 0 | intron-variant | Ube2f | GRCm38.p3 | 1:91252500 | TTGATAGCTTGTGGG[A/C]TGAAGCCCCTTTGGG | 67921 |
rs32288539 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2f | Mm_Celera | 1:91256683 | CTTTCAGATAGCTAC[A/T]GGGTGATCATGGTGA | 67921 |
rs32296152 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ube2f | GRCm38.p3 | 1:91282177 | ATGCCAGCATGTGGA[G/T]CCTTCCATTTCACCT | 67921 |
rs32308370 | snp | A/G | 0.5 | 0 | intron-variant | Ube2f | GRCm38.p3 | 1:91251300 | GATCTGTTTCTTTCA[A/G]CTTGGGAGGTTAAAC | 67921 |
rs32309596 | snp | A/G | 0.408163 | 0.193609 | upstream-variant-2KB | Ube2f | GRCm38.p3 | 1:91249142 | CCACATGGGGTGGTC[A/G]AAGGATAACTTTCTT | 67921 |
rs32339456 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2f | GRCm38.p3 | 1:91259847 | CATATCTTGGCTATC[A/G]TGAAAAATAACGGCA | 67921 |
rs32353726 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2f | Mm_Celera | 1:91268921 | CACAGAGTTGGACTC[A/G]GGTGTAGCTTTAAAG | 67921 |
rs32383483 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2f | Mm_Celera | 1:91272647 | ATTTTCTGGAGAGAC[A/G]AATTCCATTAAAGGG | 67921 |
rs32414799 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2f | GRCm38.p3 | 1:91253180 | TACTGTGTACAGAAG[A/G]TGGCATGAGAAACTA | 67921 |
rs32438358 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ube2f | GRCm38.p3 | 1:91262451 | CATTTTGGTTTTTTT[G/T]GGGGGGGGGAGTTGG | 67921 |
rs32443025 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2f | GRCm38.p3 | 1:91252562 | TGTGTTCTGACTAGG[C/T]TCATCTTTTCATATA | 67921 |
rs32462149 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ube2f | Mm_Celera | 1:91277018 | AGTGATGGGTGTCTG[G/T]TCTGTGCCAGCGGCA | 67921 |
rs32476415 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2f | GRCm38.p3 | 1:91259595 | TAAGTAATGTACTTT[A/G]TATTATTACTATGTA | 67921 |
rs32496457 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2f | Mm_Celera | 1:91254973 | ATAGCCTAAGGAAAA[A/G]TCCTGTGAAAATCTG | 67921 |
rs32497396 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Ube2f | GRCm38.p3 | 1:91265461 | GGTGTGAGGCACGCA[A/G]TGTCCAGGTGACTGA | 67921 |
rs32574639 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2f | Mm_Celera | 1:91265589 | GGTGTGATTGCTTAG[C/T]TGCAGGAGGAGAGTC | 67921 |
rs32599070 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ube2f | GRCm38.p3 | 1:91266561 | TTGTAATTCTGTTTA[C/T]ATCTAGCTGCAGTGG | 67921 |
rs32608475 | snp | C/T | 0.465374 | 0.126941 | downstream-variant-500B, utr-variant-3-prime | Ube2f | GRCm38.p3 | 1:91286339 | TCTGCCACAACTCCA[C/T]TATGACTGTCTTCCA | 67921 |
rs32636708 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2f | GRCm38.p3 | 1:91259717 | TCCGTAGCATGATGT[C/T]CTTTGCTCCATCACG | 67921 |
rs32657018 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2f | Mm_Celera | 1:91267542 | TGTTGGCTTCTGTGA[C/T]CACTATTGTAGAAAT | 67921 |
rs32662146 | snp | C/T | 0.33241 | 0.236027 | downstream-variant-500B | Ube2f | GRCm38.p3 | 1:91286566 | AGTCTTCCTGCCTGT[C/T]ATCTTCTGGGTTTAG | 67921 |
rs32689428 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2f | Mm_Celera | 1:91257555 | CTAAGTCAAGTAGGG[A/G]GTCAGATGTTGACCA | 67921 |
rs32697577 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB | Ube2f | Mm_Celera | 1:91248569 | GAGGGGGTGCCGGGG[G/T]GAGGAGCCGTAAGAA | 67921 |
rs32707918 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2f | Mm_Celera | 1:91269300 | GTTTACACATAAATT[A/C]AAATCATAAATAAGT | 67921 |
rs32751887 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2f | GRCm38.p3 | 1:91283555 | ACATGGCAGCTCACA[A/G]CTTCTGTAACTTGAG | 67921 |
rs32755947 | snp | A/T | 0.5 | 0 | intron-variant | Ube2f | GRCm38.p3 | 1:91282248 | AGAGAGTTCCTTGGT[A/T]TCCAAATTTTTAAAA | 67921 |
rs32764590 | snp | A/C | 0.33241 | 0.236027 | downstream-variant-500B, utr-variant-3-prime | Ube2f | GRCm38.p3 | 1:91286278 | AGGGCTCCTTAACAG[A/C]CTCTGTCATTGCCAT | 67921 |
rs45751146 | snp | G/T | | | intron-variant | Ube2f | Mm_Celera | 1:91260062 | GGTTGTGACCCACGG[G/T]TTGAGAACTGCTACT | 67921 |
rs45755569 | snp | A/T | | | intron-variant | Ube2f | Mm_Celera | 1:91270738 | ATGGTGATGAGCTCT[A/T]ATCCCTCTGGAACCA | 67921 |
rs45763643 | snp | C/T | | | intron-variant | Ube2f | Mm_Celera | 1:91260034 | TAACTATCTTATATA[C/T]AACCCTCAAAGAGGT | 67921 |
rs45791281 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2f | Mm_Celera | 1:91274220 | CATAATGCTGGCACA[A/G]CCTCAAAGTTCTTTC | 67921 |
rs45802138 | snp | A/C | 0.260355 | 0.249785 | upstream-variant-2KB | Ube2f | Mm_Celera | 1:91248617 | GGAAAACAAGACAAG[A/C]GTTAGCTGAGCAAAG | 67921 |
rs45820369 | snp | G/T | 0.231111 | 0.249285 | downstream-variant-500B, utr-variant-3-prime | Ube2f | Mm_Celera | 1:91286231 | TCTAAGCAAGGCTGG[G/T]AGGTGATTATGCCAT | 67921 |
rs45830487 | snp | A/G | | | intron-variant | Ube2f | Mm_Celera | 1:91254493 | GTCTGTTGAATGGGA[A/G]TACTTGTTTGAAATG | 67921 |
rs45888144 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Ube2f | Mm_Celera | 1:91271500 | AGTAGTTTAAGGTTG[G/T]AGTTGTCTTTTTGTA | 67921 |
rs46022696 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2f | Mm_Celera | 1:91264583 | CAATGTTTTAGTCTG[A/C]CATGCTCATTAAACA | 67921 |
rs46057768 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2f | Mm_Celera | 1:91276573 | CAAGCTGATGCAGCT[A/G]CTTTTGGAACACATC | 67921 |
rs46192778 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2f | Mm_Celera | 1:91284043 | TGCTTCTAGGTAGGC[A/G]CGCTAGGTTAAAGGT | 67921 |
rs46223285 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2f | Mm_Celera | 1:91270178 | CATTTTGTTCCTATG[A/G]GACAAAGGAGTTGAA | 67921 |
rs46233252 | snp | G/T | 0.459184 | 0.136902 | upstream-variant-2KB | Ube2f | GRCm38.p3 | 1:91249316 | TACTTGGTCCTAATC[G/T]GAGGACTCCTCTGCC | 67921 |
rs46255724 | snp | A/G | | | intron-variant | Ube2f | Mm_Celera | 1:91272011 | CCAGTGTTAGGGTCC[A/G]TGAATCCCTAGAGAA | 67921 |
rs46352001 | snp | C/G | | | intron-variant | Ube2f | Mm_Celera | 1:91268305 | ATTGGTGTAATGTTT[C/G]CTTGTAGTGGTACCC | 67921 |
rs46375286 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2f | Mm_Celera | 1:91271735 | TGGAATGCCCAATGT[A/G]ACTCTGTCTTGAAAA | 67921 |
rs46381015 | snp | G/T | 0.244898 | 0.249948 | upstream-variant-2KB | Ube2f | Mm_Celera | 1:91250051 | CTAGTACGATATTCC[G/T]AGGGAAGCAAGCCGC | 67921 |