SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs714300 | snp | C/T | 0.412249 | 0.190198 | intron-variant | UBA3 | GRCh38.p7 | 3:69072692 | GGTGATCTCAGACCA[C/T]CTTGTAAGATATAGA | 9039 |
rs1837182 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | UBA3 | GRCh38.p7 | 3:69068575 | AAGAGGCTGTAACCA[C/T]GTTTTTTTCTTTTTT | 9039 |
rs1866262 | snp | A/G | 0.435263 | 0.167862 | intron-variant | UBA3 | GRCh38.p7 | 3:69057036 | TCAGATTAATAAATG[A/G]CCTGCTTCATATGGA | 9039 |
rs1866263 | snp | A/G | 0.258288 | 0.249863 | intron-variant | UBA3 | GRCh38.p7 | 3:69057060 | ATATGGAACTAAAAC[A/G]TCTCTTTACTGCAGG | 9039 |
rs1866264 | snp | C/T | 0.422 | 0.181428 | intron-variant | UBA3 | GRCh38.p7 | 3:69057153 | AGCTTAGTTACACAA[C/T]CCATCCAAGAAGATA | 9039 |
rs1866265 | snp | C/G | 0.448323 | 0.15221 | intron-variant | UBA3 | GRCh38.p7 | 3:69057154 | GCTTAGTTACACAAC[C/G]CATCCAAGAAGATAT | 9039 |
rs2009602 | snp | A/G | 0.413416 | 0.189196 | intron-variant | UBA3 | GRCh38.p7 | 3:69072490 | AATGACCAATTCTCA[A/G]TCTATCTGACCTTAC | 9039 |
rs2055684 | snp | A/T | 0.487177 | 0.0790385 | intron-variant | UBA3 | GRCh38.p7 | 3:69059165 | cctcagatattgaag[A/T]gttctatgaagaaaa | 9039 |
rs2118539 | snp | A/G | 0.479177 | 0.0998894 | intron-variant | UBA3 | GRCh38.p7 | 3:69064854 | TTTATAAATTATGCA[A/G]CTTCTCTAAAGTTAA | 9039 |
rs2289245 | snp | C/T | 0.496483 | 0.0417852 | intron-variant | UBA3 | GRCh38.p7 | 3:69062898 | CTTCTAATTAACAAT[C/T]CTAAATATTAACTAG | 9039 |
rs2289246 | snp | C/T | 0 | 0 | intron-variant | UBA3 | GRCh38.p7 | 3:69071785 | AAAATTCAGAGTTCT[C/T]GAACAGGTCAAAAGT | 9039 |
rs3755717 | snp | C/T | 0.393619 | 0.204631 | intron-variant | UBA3 | GRCh38.p7 | 3:69078638 | GCCACCATACCCAGC[C/T]AATTTTTGTATTTTT | 9039 |
rs3755718 | snp | C/T | 0.477345 | 0.103991 | intron-variant | UBA3 | GRCh38.p7 | 3:69079531 | TCTGTCTCACCAGCA[C/T]AGAATTAAGCATCTG | 9039 |
rs3755719 | snp | A/G | 0.450734 | 0.149016 | intron-variant | UBA3 | GRCh38.p7 | 3:69079592 | AAATAGGCTGTTTGA[A/G]GTCAACAACCTCTTT | 9039 |
rs3755720 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | UBA3 | GRCh38.p7 | 3:69079781 | AAGGTAGATTGCCTT[G/T]TCACAGGGTCACTGC | 9039 |
rs3772979 | snp | C/T | 0.391769 | 0.205917 | intron-variant | UBA3 | GRCh38.p7 | 3:69077982 | CCACACCTACAACTA[C/T]TATGGTATCCCCAAA | 9039 |
rs3821562 | snp | G/T | 0.392325 | 0.205532 | intron-variant | UBA3 | GRCh38.p7 | 3:69074118 | TGACTAATCTTCAGA[G/T]CTAATCTTCAATTAT | 9039 |
rs3834192 | in-del | -/GGGCTGGCGAAGCGGGGAGGGGCG | | | upstream-variant-2KB | UBA3 | GRCh38.p7 | 3:69080454 | aagcggggaggggcg[-/GGGCTGGCGAAGCGGGGAGGGGCG]agGCCAGAAACACAA | 9039 |
rs3835091 | in-del | -/G/T | | | intron-variant | UBA3 | GRCh38.p7 | 3:69056970 | AACAAATTTTACATT[-/G/T]GTTTTGTGTGATTCA | 9039 |
rs3853154 | snp | A/C | 0.467337 | 0.123551 | intron-variant | UBA3 | GRCh38.p7 | 3:69076730 | catgtatcatcatgc[A/C]cagctaatttttttt | 9039 |
rs3853155 | snp | C/T | 0.445328 | 0.156035 | intron-variant | UBA3 | GRCh38.p7 | 3:69076746 | cagctaatttttttt[C/T]cttttctttttttct | 9039 |
rs3853156 | snp | C/T | 0.47023 | 0.118317 | intron-variant | UBA3 | GRCh38.p7 | 3:69077344 | ACACTTGCCTTAAGA[C/T]AGACACTATCAGTCC | 9039 |
rs3853157 | snp | C/T | 0.410568 | 0.191619 | intron-variant | UBA3 | GRCh38.p7 | 3:69077477 | GTAAGCACACCTATA[C/T]TCCTATCAAAATTAA | 9039 |
rs4365633 | snp | C/G | 0.451732 | 0.147663 | intron-variant | UBA3 | GRCh38.p7 | 3:69073186 | tcagagtaaaagcga[C/G]agcacttacagtaac | 9039 |
rs4616647 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | UBA3 | GRCh38.p7 | 3:69065064 | AGGCAAGCAGGAGAA[C/T]GAAGCTACAGCTAGA | 9039 |
rs6549179 | snp | A/T | 0.0277723 | 0.114522 | intron-variant | UBA3 | GRCh38.p7 | 3:69055544 | AAACAGAAAAAATAT[A/T]ATTAATACAAGCAAA | 9039 |
rs6549180 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | UBA3 | GRCh38.p7 | 3:69055601 | CATGTAAACAAACTA[C/T]AGAGTATTACGGTCT | 9039 |
rs6549181 | snp | A/G | 0.390464 | 0.206809 | intron-variant | UBA3 | GRCh38.p7 | 3:69065219 | GGATAGACAAACTGA[A/G]TGCCCCCCACTAACC | 9039 |
rs6549182 | snp | A/G | 0.470424 | 0.117954 | intron-variant | UBA3 | GRCh38.p7 | 3:69070090 | TACTTGCTACATATC[A/G]TTATTACCATCTTCA | 9039 |
rs6766693 | snp | C/T | 0.472896 | 0.113214 | intron-variant | UBA3 | GRCh38.p7 | 3:69070923 | TGTTGGGATTACAGG[C/T]GTAAGCCACCATGCC | 9039 |
rs6767347 | snp | A/G | 0 | 0 | intron-variant | UBA3 | GRCh38.p7 | 3:69058417 | TCCAAGTATAGTCAG[A/G]TTTCAAAAACTTAAG | 9039 |
rs6773479 | snp | C/T | 0 | 0 | intron-variant | UBA3 | GRCh38.p7 | 3:69072931 | catcagctaatcctg[C/T]tgattccatcttcaa | 9039 |
rs6775065 | snp | A/G | 0.379354 | 0.213933 | intron-variant | UBA3 | GRCh38.p7 | 3:69070989 | AAATCACTCCTTGAT[A/G]TTCTCTATATTCCAT | 9039 |
rs6777032 | snp | C/T | 0.412249 | 0.190198 | intron-variant | UBA3 | GRCh38.p7 | 3:69074082 | GCAATAAAGAAGAGG[C/T]CACTCCTTAAAGTTG | 9039 |
rs6800465 | snp | A/T | 0.477175 | 0.104362 | intron-variant | UBA3 | GRCh38.p7 | 3:69062337 | CTATAATACAGATTA[A/T]CTGAGTCACTTCACT | 9039 |
rs6804531 | snp | A/C | 0.48818 | 0.0759629 | intron-variant | UBA3 | GRCh38.p7 | 3:69058155 | cacgatggtctcgat[A/C]tcctgaccttgtgat | 9039 |
rs6807035 | snp | C/T | 0.487049 | 0.0794222 | intron-variant | UBA3 | GRCh38.p7 | 3:69058165 | tcgatatcctgacct[C/T]gtgatccgcccgccc | 9039 |
rs6807701 | snp | C/T | 0.286042 | 0.247388 | intron-variant | UBA3 | GRCh38.p7 | 3:69073792 | aggcacctgccacca[C/T]gcccggctaattttt | 9039 |
rs7614589 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBA3 | GRCh38.p7 | 3:69071729 | GTAATAAATTCTGTG[C/T]AATTTGTATTCAATG | 9039 |
rs7622883 | snp | A/G | 0.432504 | 0.170857 | intron-variant | UBA3 | GRCh38.p7 | 3:69066483 | gagccttgctctgtc[A/G]cccaggctggggtgc | 9039 |
rs7631719 | snp | A/G | 0.26326 | 0.249648 | intron-variant | UBA3 | GRCh38.p7 | 3:69068956 | AAGCTGAATATATAA[A/G]GCCTCAAAAGGTCAC | 9039 |
rs7645663 | snp | C/T | 0.445592 | 0.155704 | intron-variant | UBA3 | GRCh38.p7 | 3:69066504 | gctggggtgcagtag[C/T]gcaatttcagctcac | 9039 |
rs9823793 | snp | A/T | | | intron-variant | UBA3 | GRCh38.p7 | 3:69056708 | ACTGTAATGAAAAAA[A/T]GTTCATCTTTATATA | 9039 |
rs9831597 | snp | A/C | 0.226779 | 0.248919 | intron-variant | UBA3 | GRCh38.p7 | 3:69062360 | ACTTCACTTAGGCTG[A/C]ACTGCCTGTAAAGAC | 9039 |
rs9846769 | snp | C/G | 0.493386 | 0.0571263 | intron-variant | UBA3 | GRCh38.p7 | 3:69070738 | GTTCACTGCAGCCTC[C/G]AGATCCTGAGCTCAA | 9039 |
rs9851078 | snp | A/C | 0.146985 | 0.227789 | intron-variant | UBA3 | GRCh38.p7 | 3:69062361 | CTTCACTTAGGCTGC[A/C]CTGCCTGTAAAGACA | 9039 |
rs9872553 | snp | G/T | 0.48679 | 0.0801892 | intron-variant | UBA3 | GRCh38.p7 | 3:69068710 | GCCTCAGTCTCTAGG[G/T]AGGTGAGATTACAGG | 9039 |
rs9874969 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBA3 | GRCh38.p7 | 3:69077687 | AAATTTAGTTTCACA[A/G]AACAATTTTATTAGT | 9039 |
rs9880312 | snp | C/T | | | intron-variant | UBA3 | GRCh38.p7 | 3:69072440 | cagaaactgtacttg[C/T]caagttcaccaataa | 9039 |
rs10707788 | in-del | -/G | 0.468249 | 0.121932 | downstream-variant-500B, upstream-variant-2KB | UBA3, TMF1 | GRCh38.p7 | 3:69054291 | GGGGGGCGGGGGGGG[-/G]TGGATCACCTGAGGT | 9039 |
rs11413559 | in-del | -/T | 0 | 0 | intron-variant | UBA3 | GRCh38.p7 | 3:69066445 | TTTGTGTTTTTTTTT[-/T]GTTTTTTTGAGATGG | 9039 |
rs11544137 | snp | A/G | 0 | 0 | missense | UBA3 | GRCh38.p7 | 3:69062110 | ATTGAGTATGTAAGG[A/G]TGTTGCAGTGGCCTA | 9039 |
rs11544139 | snp | C/T | 1.65982e-05 | 0.00288077 | missense | UBA3 | GRCh38.p7 | 3:69067928 | ATTGCAATGTAGTTC[C/T]GTATCCTTTTGACAA | 9039 |
rs11705981 | snp | C/G | 0.410399 | 0.191761 | intron-variant | UBA3 | GRCh38.p7 | 3:69058142 | TCACCGTGTTAGCCA[C/G]GATGGTCTCGATATC | 9039 |
rs11709406 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | UBA3 | GRCh38.p7 | 3:69054982 | TGGCCACAATTAAAT[C/G]AGTGTTATATCAAGA | 9039 |
rs11920517 | snp | A/C | | | intron-variant | UBA3 | GRCh38.p7 | 3:69065398 | tagtacagtaccaaa[A/C]ccatgaacagaacat | 9039 |
rs12108000 | snp | A/G | | | intron-variant | UBA3 | GRCh38.p7 | 3:69077202 | AAACCAAGAGTTTGC[A/G]CGTTAATTTATGGGA | 9039 |
rs12152468 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBA3 | GRCh38.p7 | 3:69070132 | CACAAATTAAAGGGT[A/G]TGGCCTGTATCAATA | 9039 |
rs12374198 | snp | G/T | 0 | 0 | intron-variant | UBA3 | GRCh38.p7 | 3:69072823 | cagtaacttcctcat[G/T]gcagtaactccatct | 9039 |
rs12492786 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA3 | GRCh38.p7 | 3:69059635 | TTCAAGGAACACAAA[A/G]CAGGTCCGTGTAGGG | 9039 |
rs12636843 | snp | C/T | 0.0372196 | 0.131242 | downstream-variant-500B, upstream-variant-2KB | UBA3, TMF1 | GRCh38.p7 | 3:69054241 | AAAAACATggtcagg[C/T]atggtggctcatgcc | 9039 |
rs13074589 | snp | A/T | 0 | 0 | intron-variant | UBA3 | GRCh38.p7 | 3:69063432 | ATAACAATACTAAAG[A/T]CTTTACCAGCATGCC | 9039 |
rs13089408 | snp | G/T | 0 | 0 | synonymous-codon | UBA3 | GRCh38.p7 | 3:69063463 | ATTTATCCATCTTCT[G/T]GCGATGATAGAGTCC | 9039 |
rs13090606 | snp | C/T | 0.350109 | 0.229081 | intron-variant | UBA3 | GRCh38.p7 | 3:69064002 | AATAGCTAGCAATAT[C/T]TGAATAGCTACCAAC | 9039 |
rs13090922 | snp | A/C | | | intron-variant | UBA3 | GRCh38.p7 | 3:69063523 | AAAAAAAAAAAAAAG[A/C]AACTTTAGTTTTTaa | 9039 |
rs17005291 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | UBA3 | GRCh38.p7 | 3:69064440 | AGAATGTGTGTCCTC[A/C]ATCATCAGCATCAAG | 9039 |
rs17005324 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBA3 | GRCh38.p7 | 3:69074208 | CTTTAGGAAACTTGT[A/G]CATTTATAATACCTA | 9039 |
rs17852113 | snp | C/T | 0 | 0 | missense, intron-variant | UBA3 | GRCh38.p7 | 3:69080148 | ATTCTCCTTCTTTTC[C/T]TCTCCCTAAAAGAGA | 9039 |
rs34816915 | in-del | -/A | | | intron-variant | UBA3 | GRCh38.p7 | 3:69078788 | AGGTCTTAATTTTTT[-/A]AAAGAATCTCTTAAT | 9039 |
rs34996222 | in-del | -/A | | | intron-variant | UBA3 | GRCh38.p7 | 3:69068025 | ACAGGAAAAATATTT[-/A]AAATTATAATTCATA | 9039 |
rs35294510 | in-del | -/C | | | intron-variant | UBA3 | GRCh38.p7 | 3:69065236 | CCCCCCACTAACCAA[-/C]CCCACCCCCACCAAC | 9039 |
rs35335070 | in-del | -/A | 0.435263 | 0.167862 | intron-variant | UBA3 | GRCh38.p7 | 3:69068561 | CCGTATATAAAATGG[-/A]AAAAAAAAAAAAAAA | 9039 |
rs35361133 | in-del | -/T | 0.453575 | 0.145111 | intron-variant | UBA3 | GRCh38.p7 | 3:69056968 | GTAACAAATTTTACA[-/T]TTGTTTTGTGTGATT | 9039 |
rs35368832 | in-del | -/G | | | frameshift-variant | UBA3 | GRCh38.p7 | 3:69067945 | ACTACATTGCAATTA[-/G]GGAACTCTGTCATTT | 9039 |
rs35659294 | snp | A/T | | | intron-variant | UBA3 | GRCh38.p7 | 3:69065955 | TATTTTCTAATTGAA[A/T]TTTTTTTTGTTTTAC | 9039 |
rs35714240 | in-del | -/T | | | intron-variant | UBA3 | GRCh38.p7 | 3:69071940 | GCTATTGATGGATAC[-/T]TTTAATTTTACTATG | 9039 |
rs35718539 | snp | C/T | 0.393803 | 0.204501 | intron-variant | UBA3 | GRCh38.p7 | 3:69072806 | CCAGATCTTCCTCAT[C/T]GCAGTAACTTCCTCA | 9039 |
rs35749068 | in-del | -/A | | | intron-variant | UBA3 | GRCh38.p7 | 3:69072543 | TGGGTCACTTCCTCC[-/A]CCCTAAAACATGTTC | 9039 |
rs36087535 | in-del | -/A | | | intron-variant | UBA3 | GRCh38.p7 | 3:69064624 | TTTTGTGGGGAGGAG[-/A]AAAAGTACGAATTTT | 9039 |
rs55851538 | snp | A/G/T | 0.497907 | 0.0322805 | downstream-variant-500B | UBA3 | GRCh38.p7 | 3:69054526 | GAGCGAAACTCTGTC[A/G/T]CAAAAAAAAAAAAAA | 9039 |
rs56156415 | snp | C/G | 0.391583 | 0.206044 | intron-variant | UBA3 | GRCh38.p7 | 3:69066306 | CAAGCAGCCAGGACT[C/G]TGTAGTGGTATGATA | 9039 |
rs56379162 | snp | A/G | | | intron-variant | UBA3 | GRCh38.p7 | 3:69061464 | CCTCCCGAAGTGCTA[A/G]GATTGCAGGTATAAG | 9039 |
rs57973133 | in-del | -/AA | 0 | 0 | downstream-variant-500B | UBA3 | GRCh38.p7 | 3:69054547 | AAAAAAAAAAAAAAA[-/AA]TTATATTGATACAGA | 9039 |
rs58950441 | snp | A/G | 0.393619 | 0.204631 | intron-variant | UBA3 | GRCh38.p7 | 3:69072979 | ACCACCTGTCACCAC[A/G]TCCAATGCTACCATC | 9039 |
rs59034553 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | UBA3, TMF1 | GRCh38.p7 | 3:69054290 | GGAAGCCGAGGGGGG[C/T]GGGGGGGGGTGGATC | 9039 |
rs59399074 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UBA3 | GRCh38.p7 | 3:69058074 | TAGCTGGGACTACAG[A/G]GGCCCGCCACCACGC | 9039 |
rs60272924 | in-del | -/T | 0.392696 | 0.205275 | intron-variant | UBA3 | GRCh38.p7 | 3:69075730 | TTTTCTTTTTTTTTT[-/T]CTTTTTTTTGAGACG | 9039 |
rs60502579 | snp | A/T | 0.0385879 | 0.133435 | intron-variant | UBA3 | GRCh38.p7 | 3:69064034 | AAAAAATTCTAAGAA[A/T]CTAGTGAGCATTAAT | 9039 |
rs61737489 | snp | A/G | 0.00715523 | 0.0593837 | synonymous-codon | UBA3 | GRCh38.p7 | 3:69064078 | CTTACGTCGATAGAA[A/G]GTGTCGTTAAAATCT | 9039 |
rs62254241 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBA3 | GRCh38.p7 | 3:69060396 | AGTGGCTAGTAACAT[C/T]AAAGAATCCAAAGTA | 9039 |
rs62254242 | snp | A/G | 0.394354 | 0.204112 | intron-variant | UBA3 | GRCh38.p7 | 3:69061050 | AAAATGAACTAATAC[A/G]GGGTTAAAGGAACTA | 9039 |
rs71302165 | snp | C/T | 0.5 | 0 | intron-variant | UBA3 | GRCh38.p7 | 3:69068258 | TAATTAAGAGAAAAT[C/T]TGAACAGTGTTCTTC | 9039 |
rs71302166 | snp | A/C | 0.5 | 0 | intron-variant | UBA3 | GRCh38.p7 | 3:69075386 | TAAGGTTTACTTATC[A/C]CAAAGAAGAAAAAAA | 9039 |
rs71302167 | snp | C/T | 0.5 | 0 | missense, intron-variant | UBA3 | GRCh38.p7 | 3:69075453 | TCAGGAGCTCACATC[C/T]TAAGCCGCCAGCTCC | 9039 |
rs71616848 | multinucleotide-polymorphism | AC/CA | 0 | 0 | intron-variant | UBA3 | GRCh38.p7 | 3:69062360 | ACTTCACTTAGGCTG[AC/CA]CTGCCTGTAAAGACA | 9039 |
rs71618260 | in-del | -/G/T | 0.5 | 0 | intron-variant | UBA3 | GRCh38.p7 | 3:69066443 | TTATGGTTTTTTGTG[-/G/T]TTTTTTTTTGTTTTT | 9039 |
rs72924826 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBA3 | GRCh38.p7 | 3:69077509 | TTCTCACAGTAGCAC[C/T]ACAAAAGGGGAGTAT | 9039 |
rs73110235 | snp | C/T | | | intron-variant | UBA3 | GRCh38.p7 | 3:69058355 | AAGAAAAAGTAGCCA[C/T]TTTATCTCACAGTGT | 9039 |
rs73838909 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBA3 | GRCh38.p7 | 3:69065056 | TGAATGCTAGGCAAG[C/T]AGGAGAACGAAGCTA | 9039 |
rs73838912 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBA3 | GRCh38.p7 | 3:69068128 | AAATTTAGAAGGAAT[A/G]TTTTTGCCTAAGTAT | 9039 |