SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4226530 | snp | A/G | 0.42 | 0.183303 | synonymous-codon | Uba2 | GRCm38.p3 | 7:34141429 | TGAAGGGCCTTCTTC[A/G]TCTGAATCAACTATG | 50995 |
rs4226531 | snp | A/G | 0.435742 | 0.167331 | intron-variant | Uba2 | Mm_Celera | 7:34141535 | TCACCAAGGCCTCAC[A/G]CAGCAGAATCCCAGC | 50995 |
rs13472969 | snp | C/T | | | synonymous-codon | Uba2 | GRCm38.p3 | 7:34147610 | TGCACTGGATCCTCC[C/T]AACACCAACTGTTAC | 50995 |
rs13472970 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Uba2 | Mm_Celera | 7:34141164 | TGTGTTGAAGTAGGA[C/T]TAGAATTTGCAACCC | 50995 |
rs13472971 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Uba2 | Mm_Celera | 7:34141153 | AGGAATAGAATTTGC[C/T]ACCCTTTGAGCAAAG | 50995 |
rs31052409 | snp | A/G | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34158138 | AGCTACAGTAGTCCA[A/G]ATTCTTAGCAGGGAT | 50995 |
rs31059862 | snp | C/T | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34150529 | GAATCAATCTGGGAG[C/T]GGGGTGAGAGCTGCA | 50995 |
rs31135400 | snp | G/T | 0.32 | 0.24 | intron-variant | Uba2 | Mm_Celera | 7:34156888 | AGAGATGCTTCAGGG[G/T]TTAAGAACACTTTTT | 50995 |
rs31159875 | snp | A/C | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34157632 | TTGGAACTGGAGTTA[A/C]AAAAGGTTGTGAGGC | 50995 |
rs31188141 | snp | C/T | 0.5 | 0 | intron-variant | Uba2 | Mm_Celera | 7:34153588 | TTGGCAGAGTATCCC[C/T]GTAGCACTTGTGAGG | 50995 |
rs31246031 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Uba2 | Mm_Celera | 7:34146003 | AAAGTATTTCAATGT[A/G]TAAACTGCCAGAATC | 50995 |
rs31264208 | snp | C/T | 0.32 | 0.24 | intron-variant | Uba2 | Mm_Celera | 7:34154376 | AAATCAAGGCCAGCC[C/T]GGTCTACAGAGTGAG | 50995 |
rs31275486 | snp | A/G | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34144606 | ATTGGCTAGATGTGA[A/G]CAGAATGAAGATGTT | 50995 |
rs31286355 | snp | A/G | 0.32 | 0.24 | intron-variant | Uba2 | Mm_Celera | 7:34154368 | GATTTCTGAAATCAA[A/G]GCCAGCCCGGTCTAC | 50995 |
rs31302549 | snp | A/G | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34152884 | CCAGCACCACATCAC[A/G]GCTCACAACCAACCC | 50995 |
rs31352034 | snp | A/C | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34167122 | GCCCATACACGTAAA[A/C]TAAAGGAAAAAGTTT | 50995 |
rs31376825 | snp | C/T | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34150750 | GGTAACATAATGAGA[C/T]ATTACCTCAAAAACC | 50995 |
rs31382598 | snp | C/T | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34152853 | GTTTAGAACACATGC[C/T]GATTTCAAGTGCCAA | 50995 |
rs31386904 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Uba2 | Mm_Celera | 7:34151931 | CCTGGGCTCATTAGT[A/G]AAGCTGCTAGACATA | 50995 |
rs31450466 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Uba2 | Mm_Celera | 7:34163577 | GCTTCACCTCACATG[A/G]TCACCATCAGGCCGG | 50995 |
rs31468418 | snp | A/G | 0.5 | 0 | intron-variant | Uba2 | Mm_Celera | 7:34153834 | TGCAGCAGCCTCCCG[A/G]GTGCTGGGAGTCCAG | 50995 |
rs31508526 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Uba2 | Mm_Celera | 7:34152058 | GAACAGATACCTTGT[A/G]CACAGTGAGAGCTAC | 50995 |
rs31542722 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Uba2 | Mm_Celera | 7:34163734 | ATGCCCTGAGAAAGT[A/G]TAAGGCTCACTGTAA | 50995 |
rs31609737 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Uba2 | Mm_Celera | 7:34144702 | GCACTCCTTAGAAAT[C/T]GGCATTCTCAAATCC | 50995 |
rs31625695 | snp | C/T | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34156179 | CTCAGTTCTGCTGGC[C/T]ACACAGGCCCCACAA | 50995 |
rs31636221 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Uba2 | Mm_Celera | 7:34145035 | CCCACAAAGGCATCC[A/C]ATTCAAAGCAAACTG | 50995 |
rs31636317 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Uba2 | Mm_Celera | 7:34167397 | ATTCACTCCTGTCTA[C/T]TGAAAAATCTACTCT | 50995 |
rs31640852 | snp | G/T | 0.277778 | 0.248452 | synonymous-codon | Uba2 | GRCm38.p3 | 7:34165449 | GAAACAAGAACTGCC[G/T]GTTGAGGTTGCTGAC | 50995 |
rs31654099 | snp | A/C | 0.32 | 0.24 | intron-variant | Uba2 | Mm_Celera | 7:34156956 | CCCTGACTGTCCTTG[A/C]ACTCACAGAGATCCT | 50995 |
rs31699344 | snp | A/T | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34151553 | GCAAGCACAACACTT[A/T]AACATATGAAATGAA | 50995 |
rs31724898 | snp | A/G | 0.375 | 0.216506 | synonymous-codon | Uba2 | GRCm38.p3 | 7:34144594 | CTTCTTGGGGTTATT[A/G]GCTAGATGTGAGCAG | 50995 |
rs31775017 | snp | C/G | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34150558 | CACACTCTCAGGGAC[C/G]TTTTCAGATCAGCCT | 50995 |
rs31788701 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Uba2 | Mm_Celera | 7:34163778 | TATAGGGACTAGTAT[A/G]GGGGGCACACCTCTG | 50995 |
rs31789641 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Uba2 | Mm_Celera | 7:34157931 | CACCACTATTAAATA[C/G]ATCACAACCAAACAC | 50995 |
rs31794498 | snp | A/G | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34151838 | TGGTCTATAAAGCGA[A/G]TTCCAGGTTAGCCAG | 50995 |
rs31811223 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Uba2 | Mm_Celera | 7:34143625 | CACTGGCTATCCTTC[C/T]AGCAGACCTGGGCTC | 50995 |
rs31813841 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Uba2 | Mm_Celera | 7:34152763 | GAGCACTCTGTGCTC[C/T]TAACTGCTGAGCCAT | 50995 |
rs31902953 | snp | A/C | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34165277 | GATGTGCACAAGTGC[A/C]CCATAATAAGTAAAT | 50995 |
rs31925437 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Uba2 | Mm_Celera | 7:34143677 | GGCTCACAACCACTC[C/G]AGGTTTAGTGACTTT | 50995 |
rs31927160 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Uba2 | Mm_Celera | 7:34158078 | AGCAAACTTTTTAGG[C/T]ACAGGCATTTGAAAC | 50995 |
rs31929101 | snp | A/G | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34155141 | ATAAACTTTTTAAAA[A/G]TTTATTTATTATATG | 50995 |
rs31969902 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Uba2 | Mm_Celera | 7:34156434 | AGGCTTAGCTTGAAC[A/T]GTAACCAGGCGTCCC | 50995 |
rs31974330 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Uba2 | Mm_Celera | 7:34167013 | TTCAGGCTCAACATG[A/G]TGAGTCACAGCCATT | 50995 |
rs31984769 | snp | C/T | 0.32 | 0.24 | intron-variant | Uba2 | Mm_Celera | 7:34165634 | TGCATTTAAACATTA[C/T]GGGAAGAACAGCACT | 50995 |
rs31987499 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Uba2 | Mm_Celera | 7:34144698 | GACTGCACTCCTTAG[A/G]AATCGGCATTCTCAA | 50995 |
rs31987890 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Uba2 | Mm_Celera | 7:34157377 | CCCCTACAAAACAAG[C/T]ATCGTATTTTCAACA | 50995 |
rs31993656 | snp | C/T | 0.5 | 0 | intron-variant | Uba2 | Mm_Celera | 7:34143904 | ACAGAATACACATAA[C/T]TTAAAAAAATGTGAA | 50995 |
rs32045351 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Uba2 | Mm_Celera | 7:34143404 | CTTTCCTGCTGCTTT[C/T]TTTCACAAGTAAGCA | 50995 |
rs32088023 | snp | C/T | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34167374 | GAGAACAAGCATTTA[C/T]TTTTTCAATTCACTC | 50995 |
rs32111942 | snp | C/T | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34150731 | GTCCATACAGATCAG[C/T]TGGGGTAACATAATG | 50995 |
rs32169405 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Uba2 | Mm_Celera | 7:34163794 | GGGGGCACACCTCTG[A/G]AACCCTGCTCTGACA | 50995 |
rs32193138 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Uba2 | Mm_Celera | 7:34165181 | TGGTGAAGGTTCAGG[C/G]GCCTGGTCAATCCCC | 50995 |
rs32238015 | snp | A/T | 0.304688 | 0.243945 | intron-variant | Uba2 | Mm_Celera | 7:34160405 | ATTTTAGGTACTTTT[A/T]AAAATAGCTTCAAAT | 50995 |
rs32271322 | snp | C/T | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34155102 | TGACAAAGAAGTAGT[C/T]ACAATTGTTTTGTTT | 50995 |
rs32284512 | snp | A/T | 0.375 | 0.216506 | intron-variant | Uba2 | Mm_Celera | 7:34144620 | AGCAGAATGAAGATG[A/T]TATAGTTATCTTTTT | 50995 |
rs32309520 | snp | C/T | 0.32 | 0.24 | intron-variant | Uba2 | Mm_Celera | 7:34151189 | GCAATGTTGCAGTCA[C/T]ACAGCCAGAACAAGG | 50995 |
rs32349617 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Uba2 | Mm_Celera | 7:34170498 | TATTTTTATGTGTGC[A/G]TGTGCATCATGTGCA | 50995 |
rs32349742 | snp | A/G | 0.32 | 0.24 | intron-variant | Uba2 | Mm_Celera | 7:34143369 | ACTGTGCTATTTCTC[A/G]GACACTTGACCACTT | 50995 |
rs32437843 | snp | A/T | 0.207612 | 0.24638 | intron-variant | Uba2 | Mm_Celera | 7:34163626 | TCTGCTTTTAGCAGC[A/T]ATGGGAAAGAGGCAC | 50995 |
rs32445830 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Uba2 | Mm_Celera | 7:34154137 | TCCCACTGAAATAAA[C/T]TATGTTCTAGTCAAT | 50995 |
rs32479845 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Uba2 | Mm_Celera | 7:34154733 | TTGACAAAAAGAGAC[A/C]AATTTCTCAATATTG | 50995 |
rs32479847 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Uba2 | Mm_Celera | 7:34155043 | TTACTTTATTAACCA[G/T]GCTGTGAGCTGCAGC | 50995 |
rs32479850 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Uba2 | Mm_Celera | 7:34155618 | GCAGATCTGTACATA[C/T]AGCCATCAGGACACT | 50995 |
rs32480315 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Uba2 | Mm_Celera | 7:34165645 | ATTACGGGAAGAACA[A/G]CACTTAAGTCAAAGG | 50995 |
rs32480317 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Uba2 | Mm_Celera | 7:34166653 | ATTAAGCAATATGGA[A/G]CATGTTAGTTACTTT | 50995 |
rs32480319 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Uba2 | Mm_Celera | 7:34166939 | AGTCTAGGAGCCGTC[A/G]TAGATGGCTAAACAG | 50995 |
rs32480322 | snp | A/C | 0.429688 | 0.173817 | intron-variant | Uba2 | GRCm38.p3 | 7:34168106 | TATTTTAAGTTGGAG[A/C]ATATTTGAATTAAAG | 50995 |
rs32480867 | snp | C/T | 0.32 | 0.24 | intron-variant | Uba2 | Mm_Celera | 7:34158385 | ACCCTTGGCTAGCTG[C/T]TCCACAAACATTACA | 50995 |
rs32480869 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Uba2 | Mm_Celera | 7:34158722 | TTCACCATATTTAAC[C/T]ACTGTAAACACAACT | 50995 |
rs32480871 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon | Uba2 | GRCm38.p3 | 7:34158865 | GATAGGTTCTGAAGG[C/T]GTGTTCCGAATCGTA | 50995 |
rs32480873 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Uba2 | Mm_Celera | 7:34159145 | TGGGTTTTATGTTGT[C/T]AAGAAAAAATTTAAA | 50995 |
rs32481304 | snp | A/G | 0.197531 | 0.244432 | synonymous-codon | Uba2 | GRCm38.p3 | 7:34168460 | CACCAGCACCCGGCC[A/G]CCGGACACCGCCTCG | 50995 |
rs32481306 | snp | C/T | 0.277778 | 0.248452 | upstream-variant-2KB | Uba2 | Mm_Celera | 7:34168768 | TCCCAACAAAAGCTC[C/T]TTATTTAAAGGTTAA | 50995 |
rs32481308 | snp | C/G | 0.18 | 0.24 | upstream-variant-2KB | Uba2 | Mm_Celera | 7:34169382 | GGCTGGTAACACTCT[C/G]AGGATAAGCCATGGA | 50995 |
rs32481865 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Uba2 | Mm_Celera | 7:34159170 | TTTAAATTAGTGACT[A/G]CAAAATTCTTATTGT | 50995 |
rs32481867 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Uba2 | Mm_Celera | 7:34159727 | CAACGGACACCAAGA[G/T]GTTTGAAATGCTAAG | 50995 |
rs32481869 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Uba2 | Mm_Celera | 7:34159802 | GCACATCTAAACCTC[A/G]GCCTTCACACAGAAG | 50995 |
rs32481871 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Uba2 | Mm_Celera | 7:34160138 | TACCATTGTGCCCTT[C/T]ATCTTCCAATAAAAT | 50995 |
rs32481873 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Uba2 | Mm_Celera | 7:34160145 | GTGCCCTTCATCTTC[C/T]AATAAAATGTCTTGG | 50995 |
rs32482595 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Uba2 | Mm_Celera | 7:34160167 | ATGTCTTGGGTGAAG[C/T]CTCTGACAAGCTGCC | 50995 |
rs32482597 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Uba2 | Mm_Celera | 7:34160218 | GGAACAAAGAGAGCA[A/C]CTGCCTTGATGTACC | 50995 |
rs32482599 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Uba2 | Mm_Celera | 7:34160246 | ACCCATAGACATCAA[A/C]CCCTCCACTGATTCT | 50995 |
rs32482602 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Uba2 | Mm_Celera | 7:34160442 | AGGAATTCTTCAAAC[A/G]TAATCTTTAGTGTTT | 50995 |
rs32483514 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Uba2 | Mm_Celera | 7:34160652 | TCACTGACCTGGATC[C/T]AGGACTAACTAATTC | 50995 |
rs32483516 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Uba2 | Mm_Celera | 7:34160662 | GGATCCAGGACTAAC[C/T]AATTCTACAGCTGAA | 50995 |
rs32483518 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Uba2 | Mm_Celera | 7:34161418 | GACCCAAGCATCATC[A/G]TGTCTCATCTGGCAT | 50995 |
rs32483520 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Uba2 | Mm_Celera | 7:34161728 | TCAATACAGCACATG[C/T]TCATTGTGACTATGG | 50995 |
rs32483522 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Uba2 | Mm_Celera | 7:34161805 | TACAGCCTTGGTCAT[C/T]ACAGGAACACTCAAC | 50995 |
rs32483990 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Uba2 | Mm_Celera | 7:34142622 | ATGACTCATAAAACT[C/G]AAAGCCCCATTATAC | 50995 |
rs32483993 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Uba2 | Mm_Celera | 7:34143547 | ACTTTGAACACCAGG[C/G]AAGACCACATTTAAA | 50995 |
rs32484254 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Uba2 | Mm_Celera | 7:34161827 | ACACTCAACAAAACT[A/G]CAACCGAGGAATTAA | 50995 |
rs32484256 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Uba2 | Mm_Celera | 7:34161865 | AATTCACTCTAGAAA[A/C]AGACTTCTAGGAATG | 50995 |
rs32484258 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Uba2 | Mm_Celera | 7:34161876 | GAAAAAGACTTCTAG[A/G]AATGATTCCCAAGTG | 50995 |
rs32484260 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Uba2 | Mm_Celera | 7:34162424 | GTAACATGCTACTAC[C/G]CTTGCTTCTATTAAG | 50995 |
rs32484262 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Uba2 | Mm_Celera | 7:34162482 | ATGGAGCACAGTCCA[A/G]GAATCCTTCTGGCTT | 50995 |
rs32484945 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Uba2 | Mm_Celera | 7:34144192 | TACACATGTGAAGTC[A/T]GCAGGCCTGTGAGAG | 50995 |
rs32484947 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Uba2 | Mm_Celera | 7:34144962 | GTGTGCTATCAGGCA[C/T]GTAGGAATTCAGCCC | 50995 |
rs32484949 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Uba2 | Mm_Celera | 7:34145243 | CACACTTCCAAAATA[A/G]CCAGCCAACATGACC | 50995 |
rs32484951 | snp | A/G | 0.18 | 0.24 | intron-variant | Uba2 | Mm_Celera | 7:34146035 | GTGCATCAGGTCACT[A/G]ACAAGTCCCTGAGGT | 50995 |
rs32484953 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Uba2 | Mm_Celera | 7:34146132 | AGCAAATGCCATGCT[A/G]ACTCATGCAATGAGC | 50995 |