SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs704533 | snp | A/G | 0.47614 | 0.106587 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23443336 | AGGGAACATAATCCC[A/G]AGAAGTAGAGTGAGA | 7325 |
rs704534 | snp | A/G | 0.491316 | 0.0653198 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23431855 | ATTCTTACTGAAAAT[A/G]TTTTGAATTAATTTT | 7325 |
rs704535 | snp | C/T | 0.294576 | 0.245994 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23394906 | TTGCTATTGTTACAC[C/T]AGCCTCTAAATCAGC | 7325 |
rs716456 | snp | C/G | 0.498632 | 0.0261223 | intron-variant, utr-variant-3-prime | UBE2E2 | GRCh38.p7 | 3:23338799 | ttaagtaaattcaaa[C/G]gggagaaaggaacac | 7325 |
rs716457 | snp | A/G | 0.475789 | 0.107327 | intron-variant, utr-variant-3-prime | UBE2E2 | GRCh38.p7 | 3:23338828 | ACACTTTCTTGCCAT[A/G]GAATTCCAATTAGTA | 7325 |
rs718331 | snp | A/T | 0.262159 | 0.249704 | intron-variant, utr-variant-3-prime | UBE2E2 | GRCh38.p7 | 3:23338768 | ccataaaataaaaAG[A/T]GGTATCCAGATATaa | 7325 |
rs778457 | snp | A/T | 0.288127 | 0.247076 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23403128 | AAGATAAAAAAGACT[A/T]GTGAAATTGAAATTA | 7325 |
rs778458 | snp | C/T | 0.288127 | 0.247076 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23403729 | CTCAGGAGGCTGAGG[C/T]TTGAGAATTGCTTGA | 7325 |
rs778459 | snp | A/G | 0.435407 | 0.167703 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23404418 | ATATTAGTCACCTTA[A/G]ACTTGTTACTCATAG | 7325 |
rs778460 | snp | A/G | 0.490673 | 0.0676508 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23405874 | CAAGTCTGGATCAAA[A/G]TGATAGAAATTCCAT | 7325 |
rs778461 | snp | C/G | 0.434543 | 0.168653 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23406132 | ATTGACTGCCTGGAA[C/G]GCAGAATTATAAAGT | 7325 |
rs778462 | snp | A/C | 0.43555 | 0.167544 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23406168 | ACAGTGTTAGACAAT[A/C]TTTCCAAGGCTCTCC | 7325 |
rs778463 | snp | G/T | 0.267908 | 0.249358 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23407292 | TCAGATGACATCTGA[G/T]ACAACCTGGTATAAA | 7325 |
rs778464 | snp | A/G | 0.444799 | 0.156695 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23407639 | TGTGTTTGTGTGTGC[A/G]TGCGTGCATGTGTGT | 7325 |
rs778465 | snp | A/G | 0.275999 | 0.248644 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23471370 | CTGCTAGTATTTGGG[A/G]GTTTATAAGGATACT | 7325 |
rs778466 | snp | C/G | 0.474 | 0.111014 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23469562 | TAAGCATGCAATATA[C/G]GGAGGTTCTTACTGG | 7325 |
rs778467 | snp | G/T | 0.426507 | 0.177046 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23412603 | TAATTTAAGTCCTGT[G/T]TCTGAGTTGAACTGC | 7325 |
rs778468 | snp | C/T | 0.428786 | 0.174744 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23412070 | TAGATATGGGGTCCA[C/T]ACTGTCATCTAAGTG | 7325 |
rs778469 | snp | A/G | 0.287606 | 0.247155 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23411939 | AGCAACTGTGATTTC[A/G]TTTGTACTGCAATTA | 7325 |
rs778470 | snp | A/G | 0.470521 | 0.117772 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23411169 | CTGAGGCGGAAGAGC[A/G]TGCTGCCTGAATCCT | 7325 |
rs778471 | snp | A/G | 0.423413 | 0.180077 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23410619 | ACATATTCTAATTTC[A/G]CAGGGTTATTTCGGG | 7325 |
rs778472 | snp | A/G | 0.499 | 0.0223418 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23464408 | ATGTCAATGGTTGAT[A/G]TTATGCAGATACTAA | 7325 |
rs778473 | snp | C/T | 0.356597 | 0.226135 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23463188 | CTCTGAAAGAATTAA[C/T]GTTTTAAGGGGGAAA | 7325 |
rs778474 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23462656 | GAATTGGTCTGGTCC[G/T]TTCTTCAGCCTTGTA | 7325 |
rs778475 | snp | A/T | 0.421526 | 0.181876 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23462015 | AGTGGGATATTTATG[A/T]CAAATCACTTTAGCT | 7325 |
rs778476 | snp | A/G | 0.418974 | 0.184249 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23459505 | TGGATTTGTAAAAAC[A/G]TTATGGTCCTGTTAC | 7325 |
rs778477 | snp | C/T | 0.487432 | 0.0782705 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23458519 | gaggcaggagcatgg[C/T]gtgaacccggcaggc | 7325 |
rs778478 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23457434 | aggtggctatttaag[A/T]ctagattttcagtgc | 7325 |
rs778479 | snp | C/T | 0.372794 | 0.217765 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23457023 | CAGCATTCTTCTTAT[C/T]ACAAGTAATAAAATC | 7325 |
rs778480 | snp | C/T | 0.413582 | 0.189052 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23457001 | AATAAAATCTCCTTG[C/T]TGAATCCTCGATTAT | 7325 |
rs778481 | snp | C/T | 0.236724 | 0.249647 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23456485 | accaaagagtaattt[C/T]gactttcaagtgtta | 7325 |
rs778482 | snp | A/T | 0.491783 | 0.0635686 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23456174 | gcctaaagatattga[A/T]ttgctgcaatcttat | 7325 |
rs778483 | snp | A/G | 0.374 | 0.217081 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23453549 | AGTTCTAGTCTTCAA[A/G]GATGCATACAATTTT | 7325 |
rs778484 | snp | A/G | 0.436692 | 0.166271 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23390737 | tgtgctccctctccc[A/G]caaggggtttgagct | 7325 |
rs778485 | snp | A/C | 0.492337 | 0.0614248 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23391606 | TTAATAAATAAATTA[A/C]ATTCAGGTATTTCTT | 7325 |
rs778486 | snp | A/G | 0.432063 | 0.171327 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23393043 | tgaaggaagattatc[A/G]taaaagcaagaaagt | 7325 |
rs778487 | snp | G/T | 0.491936 | 0.0629843 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23395759 | CTAGGAAGGAGAATC[G/T]GGGTATAAGTGCTCT | 7325 |
rs778488 | snp | A/T | 0.429388 | 0.174127 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23395973 | CCATATTAATTATCC[A/T]AATTTTATTAATTTG | 7325 |
rs778489 | snp | A/G | 0.329084 | 0.237162 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23478360 | TGCCATTTTCTCAGA[A/G]TTAGCCACTTTGTAA | 7325 |
rs778490 | snp | C/T | 0.48692 | 0.0798058 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23476549 | TGCCACCAGACCCCA[C/T]TAATTTTTAAATGTT | 7325 |
rs778491 | snp | A/G | 0.39009 | 0.207062 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23474609 | TAAATGTGACCATAT[A/G]TAAATTTAAACTTTT | 7325 |
rs778492 | snp | A/G | 0.258288 | 0.249863 | intron-variant, nc-transcript-variant | UBE2E2, LOC105376991 | GRCh38.p7 | 3:23426270 | tctcatcatgcatat[A/G]ATACACCTATTGTTG | 7325 |
rs778493 | snp | G/T | 0.338069 | 0.233974 | intron-variant, nc-transcript-variant | UBE2E2, LOC105376991 | GRCh38.p7 | 3:23424610 | CTGCTCCAGGCATAA[G/T]GTTTCATTTAAGAAT | 7325 |
rs778494 | snp | A/G | 0.491987 | 0.0627894 | intron-variant, nc-transcript-variant | UBE2E2, LOC105376991 | GRCh38.p7 | 3:23423644 | TTGCATGTCCAGTGC[A/G]TGTATTTATTTCTAG | 7325 |
rs778495 | snp | C/T | 0.02016 | 0.0983543 | intron-variant, nc-transcript-variant | UBE2E2, LOC105376991 | GRCh38.p7 | 3:23423024 | AAGGCTTGGTTTTTC[C/T]GTGTGTCTGCTTACA | 7325 |
rs778496 | snp | C/T | 0.474182 | 0.110646 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23438653 | TAATTAAAGTATTAA[C/T]ATTTTTCCTTTTCAT | 7325 |
rs778497 | snp | G/T | 0.288646 | 0.246995 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23437553 | TTTTACCCTTAATGA[G/T]GAAGATGAAGGTCAG | 7325 |
rs778498 | snp | C/G | 0.494057 | 0.0541878 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23436325 | AATATCATGGAACAG[C/G]AGAATGAACCTGGGC | 7325 |
rs778499 | snp | A/T | 0.475525 | 0.107882 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23434787 | CTAATAAAGCATTAC[A/T]CTGAGAGAATTTCCT | 7325 |
rs778500 | snp | A/G | 0.475965 | 0.106957 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23434207 | GCAATTTTGTTGTAC[A/G]TTAACAATCATCCAC | 7325 |
rs778501 | snp | A/G | 0.474723 | 0.109542 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23433376 | TTTATCTAGAAGCAC[A/G]CATAAAACAAAATTC | 7325 |
rs778502 | snp | C/T | 0.31014 | 0.242659 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23433120 | TAATTATTTTCTGTA[C/T]GAATAAACAACTGGG | 7325 |
rs778503 | snp | A/G | 0.422158 | 0.181278 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23431962 | AAGCTCTCACAGACA[A/G]GTCATATGAAACCAC | 7325 |
rs778504 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23397633 | ATGGGATCATATACC[A/G]TCTACATTTTGGTGT | 7325 |
rs778505 | snp | A/C | 0.436408 | 0.16659 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23398324 | TCTCAAAAAAAAAAA[A/C]AAAAAAAAACTTGGA | 7325 |
rs778506 | snp | A/G | 0.486067 | 0.0822953 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23399153 | catagatagaacatc[A/G]tttcttaccatagta | 7325 |
rs778507 | snp | C/T | 0.486984 | 0.079614 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23399214 | caagttaagaacgtt[C/T]atcttttcacttaaa | 7325 |
rs778508 | snp | C/T | 0.48692 | 0.0798058 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23399778 | CCTGCTCAACAATAC[C/T]TTACATTATAATGTA | 7325 |
rs778509 | snp | A/C | 0 | 0 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23401217 | ggagaaagatcaaga[A/C]gctagtagagtatgg | 7325 |
rs778510 | snp | C/T | 0.46885 | 0.12085 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23489408 | tgtgaagtgcacatg[C/T]gaaggatctaggctg | 7325 |
rs778511 | snp | C/T | 0.29278 | 0.246313 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23489359 | ctagtacctaatgac[C/T]tgacactgtctccca | 7325 |
rs778512 | snp | C/T | 0.295343 | 0.245854 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23489142 | aaaaactgtcttcta[C/T]gaaactggtccctag | 7325 |
rs778513 | snp | A/G | 0.25801 | 0.249872 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23489072 | GAAGACTCTTATCCT[A/G]TCACTACATCTGCCA | 7325 |
rs778514 | snp | A/G | 0.411074 | 0.191194 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23488841 | AGAACACTTGGGCCT[A/G]TGAGCTAGCAAATGT | 7325 |
rs778515 | snp | A/G | 0.427271 | 0.176281 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23487769 | CTATTACCGtaacat[A/G]gtggtaaagaaagta | 7325 |
rs778516 | snp | A/G | 0.388398 | 0.208197 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23487578 | ggtgcctagaacagt[A/G]cctggctcatagtaa | 7325 |
rs778517 | snp | G/T | 0.378765 | 0.214288 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23487486 | Gacactggccacagt[G/T]ggggaggcacatctg | 7325 |
rs778518 | snp | A/G | 0.39009 | 0.207062 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23486812 | ctttttccaggcccg[A/G]ccatggaccagtcag | 7325 |
rs778519 | snp | G/T | 0.293294 | 0.246223 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23486102 | aggtgtgggatccag[G/T]ccagtagtgcaagct | 7325 |
rs778520 | snp | C/T | 0.347914 | 0.230028 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23485628 | CCACATACTCTGAAA[C/T]AGTGGCTTTACAATT | 7325 |
rs778521 | snp | C/T | 0.485118 | 0.0849685 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23484134 | GAAAGCGGGTTGCCC[C/T]TTGGAAGAACAGCAG | 7325 |
rs778522 | snp | A/G | 0.391583 | 0.206044 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23483651 | ACTGAATGAGAAACT[A/G]CATTTTTGACAAGGT | 7325 |
rs778523 | snp | C/G | 0.41325 | 0.18934 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23453227 | AAAACACCACAACTA[C/G]GTTGATTTAACTGAC | 7325 |
rs778524 | snp | C/T | 0.418491 | 0.184691 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23453021 | TTTCTAAGGATACTA[C/T]TAAAAATGGGACATA | 7325 |
rs778525 | snp | C/T | 0.3746 | 0.216737 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23452821 | AACTCTGTTAGATCA[C/T]AGGCATTTTGTAGTA | 7325 |
rs778526 | snp | C/T | 0.419616 | 0.183658 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23452740 | CTGACATACCCTCCT[C/T]TTCACAGAATGATAA | 7325 |
rs778527 | snp | C/G | 0.356811 | 0.226034 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23452545 | TATAAATTTTAACTG[C/G]TCAGTGTGCACTAGA | 7325 |
rs801277 | snp | A/G | 0.429538 | 0.173972 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23487530 | ACTATTGATGGCGGT[A/G]GTAGCGCAACCGGAT | 7325 |
rs809640 | snp | A/C | 0.306182 | 0.243605 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23485289 | ggccaacacagtgaa[A/C]ccttgtctctattaa | 7325 |
rs875442 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23523599 | TTATTCAAGGGCCAG[A/C]TAATATTCCTATGGG | 7325 |
rs875443 | snp | C/T | 0.31721 | 0.240796 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23524585 | GATCCATGAGTTGTA[C/T]TGTGGAAAGAATATA | 7325 |
rs903518 | snp | C/T | 0.455502 | 0.142369 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23295477 | CCCGTTGGACAGAGA[C/T]CTGTTCTCTTATTAA | 7325 |
rs903519 | snp | A/G | 0.370162 | 0.219229 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23233134 | CTACAGGCTCAGGCT[A/G]TTGCCAACTCCCTCA | 7325 |
rs903520 | snp | A/G | 0.261608 | 0.24973 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23232985 | TGCTTAAAGCAATGG[A/G]CTGTGCCACTCTTAG | 7325 |
rs923995 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23209858 | GGTTATTCCAAGGTA[C/T]TAGAGTATTCAGTTT | 7325 |
rs923996 | snp | A/G | 0.312837 | 0.241974 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23209881 | TTCAGTTTCCCTTTC[A/G]TGGGGGTGTATTGCT | 7325 |
rs931609 | snp | A/G | 0.257454 | 0.249889 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23370932 | TTTAAACGTTTTCAA[A/G]TTTTATAAGCAACAG | 7325 |
rs952134 | snp | A/G | 0.4983 | 0.0291038 | intron-variant, utr-variant-3-prime | UBE2E2 | GRCh38.p7 | 3:23333068 | CTGCAGGTCCCACTG[A/G]TATCTCTATATTGGT | 7325 |
rs983288 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23431880 | TACAGTATGTGGGCC[A/G]AGTTGGCCCATTCTT | 7325 |
rs999764 | snp | A/G | 0.45866 | 0.137698 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23469847 | ACAAGAAAACAATTT[A/G]TGCTTATTTTAGAAA | 7325 |
rs1007332 | snp | C/T | 0.084364 | 0.187256 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23472368 | AGAAACAAAATTTCA[C/T]CAGTCCTTATTCTGA | 7325 |
rs1011754 | snp | A/G | 0.0797672 | 0.183087 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23499566 | TAAATTCCAGCCTTT[A/G]TGTAATTTCTAAGCA | 7325 |
rs1013460 | snp | G/T | 0.485528 | 0.0838238 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23216369 | CAAATTCTTGTTTTG[G/T]TTTTTAAAGATACTT | 7325 |
rs1027379 | snp | A/G | 0.48679 | 0.0801892 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23304297 | TTGATGTCAAAAACC[A/G]CTGTTTTTTTCCACA | 7325 |
rs1027380 | snp | A/G | 0.316 | 0.241131 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23304724 | agtggtaatttctgt[A/G]ggttaattgctatgt | 7325 |
rs1054048 | snp | A/C | 0.175576 | 0.238665 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23344450 | TATGAAGCAAACTAA[A/C]GCCTTTGAATTTTTT | 7325 |
rs1353322 | snp | A/G | 0.499104 | 0.0211472 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23348810 | GGTTTCTCTGGGTAT[A/G]GCCTGCAAAACCCAC | 7325 |
rs1390083 | snp | A/T | 0.363359 | 0.222822 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23257675 | CATGGCTGGTTTTAC[A/T]TTTTTTTTGGTTCAT | 7325 |
rs1390084 | snp | A/G | 0.262159 | 0.249704 | intron-variant, utr-variant-3-prime | UBE2E2 | GRCh38.p7 | 3:23338769 | cataaaataaaaAGT[A/G]GTATCCAGATATaat | 7325 |
rs1391756 | snp | C/G | 0.293037 | 0.246268 | intron-variant | UBE2E2 | GRCh38.p7 | 3:23506254 | TCAAGTTCTTTCTTA[C/G]ATTTTGAATTGCCTA | 7325 |