SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs873255 | snp | G/T | 0.140581 | 0.224783 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059873 | AAACTAGCAGTGTAC[G/T]GTGAGCGCAAAAGTT | 10477 |
rs873256 | snp | A/T | 0.495407 | 0.0477027 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059624 | TAAATACCAGATTTC[A/T]AAGAGTTAGTACCAA | 10477 |
rs908734 | snp | C/T | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059947 | AATCACAAACACTAA[C/T]TGGATAGCTAATTCA | 10477 |
rs908735 | snp | A/G | 0.139564 | 0.224285 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059158 | AATGGTTAATACTGT[A/G]TATCTCAGCAACAGA | 10477 |
rs908736 | snp | A/G | 0.267908 | 0.249358 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059046 | AAATTACGGCAAATC[A/G]TATACAGTACTATAT | 10477 |
rs1040227 | snp | C/T | 0.221737 | 0.248397 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021297 | TCAATTTTTAACACT[C/T]GGATAAAGACAGAAA | 10477 |
rs1107786 | snp | A/G | 0.277867 | 0.248442 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999173 | TCGAATTTATTTATT[A/G]TGATAAGAGAATAAT | 10477 |
rs1401124 | snp | C/G | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007378 | TTAGCCCTACATGTT[C/G]CTCCCTATTGATAAT | 10477 |
rs1401125 | snp | A/G | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007462 | TCCGGAAAAGAAGAG[A/G]AAGTGGAGATAAGTA | 10477 |
rs1401126 | snp | A/G | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007696 | TGTGGAGGGGGCCCA[A/G]CAGTGAATGGAGGCC | 10477 |
rs1401127 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014387 | TATTTTAGGTGTATA[C/G]ATGGCAGTATGTATC | 10477 |
rs1401128 | snp | A/C | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015835 | ATACTAGAGATGATA[A/C]CCACAAAACTTAAGT | 10477 |
rs1401129 | snp | A/C | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029568 | TTGCTAGATAAAAAA[A/C]AAGTTTTTAGATAAA | 10477 |
rs1401130 | snp | A/T | 0.47023 | 0.118317 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029486 | GATGTACAATACTTG[A/T]ATACAGAAAATTACA | 10477 |
rs1401131 | snp | A/G | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026593 | TAATCCCCATTATAT[A/G]CAGCTTTCACCCCTC | 10477 |
rs1401132 | snp | A/G | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026399 | AAATGGTCTATGAGA[A/G]ACTGCAGTTATTTGT | 10477 |
rs1401134 | snp | C/T | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062633 | AGTAACATGATCATA[C/T]GTATATTTTAATATT | 10477 |
rs1401135 | snp | A/C | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062616 | TATATTTTAATATTC[A/C]AGTTAGGAAAGTCCC | 10477 |
rs1518454 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007061 | CAGTCTCAGGTCTCT[C/T]TCATCTCCCAGTCCT | 10477 |
rs1518455 | snp | C/T | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007199 | ATCAGATCTTAATGC[C/T]CACTGCCCCTTTGAG | 10477 |
rs1518456 | snp | A/T | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008221 | TTCTTCTGCATGAGG[A/T]TTGGATGGAAGCTGT | 10477 |
rs1518457 | snp | C/T | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009355 | TTTTGTTTATTTTGG[C/T]ATATACACCAAAATA | 10477 |
rs1518458 | snp | G/T | 0.257454 | 0.249889 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013097 | TTCCCGAGTAGCTGG[G/T]ACTACAGTCATGCAC | 10477 |
rs1518459 | snp | A/G | 0 | 0 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022400 | CTTTTATTTCCCCTA[A/G]GAGTAATGGTTCAGT | 10477 |
rs1829365 | snp | A/T | 0.243347 | 0.249911 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020894 | TCTAAAAACTTAATA[A/T]AAAACTTAATCCATC | 10477 |
rs1829366 | snp | A/T | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020873 | TTAATCCATCCAGTC[A/T]CCTACAACCATATCA | 10477 |
rs1850640 | snp | A/G | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009458 | AAACAAAGTAAGATG[A/G]AAGTCCACCACATAC | 10477 |
rs1949453 | snp | A/T | 0.447162 | 0.153712 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046047 | GGCAAGGACCTTGTA[A/T]GTTCTTCTGTTCATC | 10477 |
rs2030242 | snp | A/G | 0.494855 | 0.0504572 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019066 | TGAGGCACGAGAATC[A/G]CTTGAACCTGGGAGG | 10477 |
rs2048975 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025924 | CGTTTATGTGCAAAT[G/T]TCCATAAATCCATTG | 10477 |
rs2048976 | snp | C/G | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024071 | CTACAACGACAGTAT[C/G]AATAGGAGAAAAATG | 10477 |
rs2048977 | snp | A/C/G | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023870 | ACATTTATCTAGCAC[A/C/G]AACTTACGTGGAGGG | 10477 |
rs2090558 | snp | C/T | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029160 | ACTTGATGAATAGAA[C/T]GGAAGAGCCCAACAC | 10477 |
rs2102855 | snp | A/G | 0.278664 | 0.248351 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028928 | AGACCTTGGGACAGA[A/G]AGTAATTTCTTAACC | 10477 |
rs2292855 | snp | C/T | 0.21845 | 0.248001 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061058 | AGATTCCATTAATGA[C/T]GGTGACAAAATAATT | 10477 |
rs2292856 | snp | A/G | 0.140242 | 0.224618 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060987 | AGAAACTTTTGGCCT[A/G]GTCTACTTCAAATGG | 10477 |
rs2368188 | snp | A/G | 0.147656 | 0.228091 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054668 | CAAATATTTTCTCCA[A/G]GACTGTTGCCTGCCT | 10477 |
rs2368189 | snp | A/C | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059568 | TTTCAACATGTAATC[A/C]GTGTAAGAGTATTGT | 10477 |
rs2368190 | snp | C/T | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059597 | GTTAATGAAATCTTA[C/T]ACATTTTCTTTTTGG | 10477 |
rs2368191 | snp | A/G | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059928 | TTCTCGGCAACTCCA[A/G]TTATGAATTAGCTAT | 10477 |
rs2368192 | snp | A/T | 0 | 0 | missense | UBE2E3 | GRCh38.p7 | 2:181062865 | AGGATAGCCAGACAG[A/T]GGACCAAGAGATACG | 10477 |
rs2368193 | snp | A/G | | | synonymous-codon | UBE2E3 | GRCh38.p7 | 2:181062885 | CAAGAGATACGCAAC[A/G]TAATTCACATAATTT | 10477 |
rs2887186 | snp | A/G | 0.44651 | 0.154543 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030744 | TTAACTACAAGTCCC[A/G]TCTCTATATTGTATA | 10477 |
rs3060035 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007501 | AACTAAGTATAATTG[-/T]TTTTTTTTTTTTTCT | 10477 |
rs3060037 | in-del | -/T | 0 | 0 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008922 | TTTTTTTTTTTTTTT[-/T]ATCAGACTAGGGTAT | 10477 |
rs3215269 | in-del | -/C | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061506 | TATTAAAGTAGTTGC[-/C]TAAAAGCATACAGCA | 10477 |
rs3792220 | snp | A/G | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062468 | AGCAGAAATATAACC[A/G]CCTAGTATACTTCCA | 10477 |
rs3838591 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062184 | AGATAGTTTTTTTTT[-/T]ACTGGCTATGGTTTG | 10477 |
rs4018770 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018599 | GTTTCAATTTCTGTG[-/T]TTTTTTTTTTTTTTT | 10477 |
rs4018771 | snp | C/T | | | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181062957 | TGCAAATCTTTATAG[C/T]CTTTACAATACGGAC | 10477 |
rs4018772 | snp | G/T | | | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063090 | TAGATTAGTTATGTT[G/T]AAAACGCCTACTTGC | 10477 |
rs4018773 | snp | A/G | | | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063190 | CAAATATTATAGTGC[A/G]TTTTAGCCTAATTCA | 10477 |
rs4018774 | snp | G/T | | | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063203 | GCATTTTAGCCTAAT[G/T]CATTATCTGTATGAA | 10477 |
rs4018775 | snp | C/G | | | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063219 | CATTATCTGTATGAA[C/G]TTATAAAAGTAGCTG | 10477 |
rs4018776 | snp | A/G | | | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063241 | AAGTAGCTGTAGATG[A/G]CTAGGAATTATGTCA | 10477 |
rs4077213 | snp | C/T | 0.278133 | 0.248412 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999902 | GCCTGTTTATTTGTC[C/T]ATATAACTGCTTTTT | 10477 |
rs4077214 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999690 | GTCATGTGGATGTCC[C/T]TGATGTACAACAAGG | 10477 |
rs4286243 | snp | C/G | 0.495671 | 0.0463237 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016014 | AGATTAAAATTTGTT[C/G]AATTCAACTAGCTTT | 10477 |
rs4299301 | snp | A/T | 0.461148 | 0.133852 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982678 | CTAGAAAATTTGCAA[A/T]TTCAGGCCTTTGCTA | 10477 |
rs4343437 | snp | A/T | 0.0562307 | 0.157967 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994937 | agtcaagagaatcgt[A/T]aatgtaaatattaaa | 10477 |
rs4346343 | snp | A/G | 0.308414 | 0.24308 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002320 | TAATGTTTATTTTCT[A/G]TTGCTCACTGCGTTA | 10477 |
rs4362519 | snp | C/G | 0.470132 | 0.118498 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024335 | AAGACTTCATCCTAC[C/G]ATTCTACCATCCTAT | 10477 |
rs4366861 | snp | A/T | 0.277067 | 0.24853 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988301 | GTCAGTTCACCAGAT[A/T]ATTGAGTACAAGTAC | 10477 |
rs4414647 | snp | A/G | 0.494692 | 0.0512434 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018015 | TTTCTCTTTCTACCT[A/G]GAAGACCACCCTAAT | 10477 |
rs4427978 | snp | A/G | 0.0562307 | 0.157967 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991059 | tattcatacaggtgg[A/G]ataagtggaagctac | 10477 |
rs4508560 | snp | G/T | 0.479663 | 0.0987666 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002458 | AAACTTAGGAATGAT[G/T]ACGAACGAAGAAAAC | 10477 |
rs4531897 | snp | C/T | 0.277867 | 0.248442 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999216 | AGGGTATTACATGAC[C/T]GCAAAGAATGGCAGT | 10477 |
rs4563182 | snp | G/T | 0.278399 | 0.248382 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988450 | GAACATGCATAAGAT[G/T]AATGATATTTAATTC | 10477 |
rs4588146 | snp | C/T | 0.0569829 | 0.158885 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988424 | GAACAAATATTGTAT[C/T]CCTTTTAAAGGAACA | 10477 |
rs4595925 | snp | C/T | 0.296619 | 0.245615 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979589 | AGTAGCTGGAGAAGG[C/T]CTGGGTGGCAAACAG | 10477 |
rs4599066 | snp | C/T | 0.278399 | 0.248382 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988418 | ATAGATGAACAAATA[C/T]TGTATTCCTTTTAAA | 10477 |
rs4666662 | snp | A/T | 0.277867 | 0.248442 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992321 | AAGATAATCTTTAAT[A/T]CTTAAACACAAGTAT | 10477 |
rs4666663 | snp | G/T | 0.2776 | 0.248472 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992565 | TATATCTGTGTATCT[G/T]GTAGCTCTGACATTT | 10477 |
rs4666664 | snp | A/G | 0.2776 | 0.248472 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992657 | CACCCCACCATGCCT[A/G]ACTAACTTTTTTTTT | 10477 |
rs4666667 | snp | A/C | 0.277867 | 0.248442 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998339 | TGATTTAGTAGGCCA[A/C]GGGTGGCCTACTAAA | 10477 |
rs4666668 | snp | C/T | 0.257454 | 0.249889 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998537 | TAAGATCATGTTTCC[C/T]ACTTGATTTTAGTTG | 10477 |
rs4666669 | snp | G/T | 0.277867 | 0.248442 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998551 | CTACTTGATTTTAGT[G/T]GCTAGTCATTTCTTA | 10477 |
rs4666670 | snp | A/G | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005784 | GTATTTAATATTTTT[A/G]TGAATCTGAAGTTAC | 10477 |
rs4666684 | snp | G/T | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041761 | CTGTGGTAAGCTCTT[G/T]TCAAATAAGAATTAT | 10477 |
rs4666685 | snp | C/T | 0.27893 | 0.24832 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041828 | ACAACCAAACCACTG[C/T]CAGGAGGCAGCGTGG | 10477 |
rs4666991 | snp | A/C | 0.278598 | 0.24886 | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990270 | ACATTAGTAGGTAGA[A/C]GTCAGTGGTACTGCT | 10477 |
rs4666992 | snp | G/T | 0.277334 | 0.248501 | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990276 | GTAGGTAGACGTCAG[G/T]GGTACTGCTGAATAC | 10477 |
rs4666993 | snp | A/G | 0.2776 | 0.248472 | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990278 | AGGTAGACGTCAGTG[A/G]TACTGCTGAATACCC | 10477 |
rs4666996 | snp | C/G | 0.277067 | 0.24853 | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990492 | CTTCCTCAGCTGATT[C/G]TTCACTTCCTGCTAC | 10477 |
rs4666997 | snp | A/G | 0.277334 | 0.248501 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990566 | TGTGTGTTATTTTTT[A/G]TGTGAAACCACAGGA | 10477 |
rs4667004 | snp | C/T | 0.2776 | 0.248472 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997794 | TTTGTTTACATCTCT[C/T]GTTGCCTAGGATGGC | 10477 |
rs4667005 | snp | A/G | 0.290718 | 0.246662 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997852 | TTAAAGCCTATTTCA[A/G]ATGTTACATCTTTTT | 10477 |
rs4667006 | snp | A/G | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000603 | TCTGTCGCCCAGGCT[A/G]CAGTGCAGTGGCTTG | 10477 |
rs4667007 | snp | C/T | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000789 | TCGATCTCCTGATCG[C/T]GTGATCCGACCACCT | 10477 |
rs4667008 | snp | C/T | 0.288127 | 0.247076 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000876 | TGATTGAAACTGTTA[C/T]GTAAAGTAAGAATTC | 10477 |
rs4667020 | snp | A/G | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023595 | GCCGCCTGATAGAAC[A/G]GTAGCCATGCTCTTT | 10477 |
rs4667030 | snp | C/G | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030974 | AGTTTATACTATTAC[C/G]TTTGTTACCTTTTCT | 10477 |
rs4667035 | snp | A/G | 0.278133 | 0.248412 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035416 | GTATTTATAAAAAAT[A/G]TGAATTACTTTTTAA | 10477 |
rs4667036 | snp | A/G | 0.495596 | 0.0467178 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035497 | TTATATATTACTCTT[A/G]GTAATATTATATATG | 10477 |
rs4667037 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035509 | CTTAGTAATATTATA[G/T]ATGTATACTTTAATA | 10477 |
rs4667041 | snp | A/G | 0.278133 | 0.248412 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050214 | ATTGAAGGTGTTTCA[A/G]GCAAGAGTTACATAC | 10477 |
rs4990275 | snp | C/G | 0.277334 | 0.248501 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008934 | TTTTATCAGACTAGG[C/G]TATAATTTGTTTTAT | 10477 |
rs5836758 | in-del | -/T | 0.288906 | 0.246954 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006385 | GTTTGTGATTTCAGA[-/T]TTTTGTTGCCTTCCA | 10477 |
rs5836761 | in-del | -/TT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008907 | TCTTGCAGTATGTGC[-/TT]TTTTTTTTTTTTTTA | 10477 |
rs5836762 | in-del | -/G | 0.278664 | 0.248351 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009025 | TTATAGCAGTGCTAA[-/G]GATACTTATTCTAAA | 10477 |