SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8568 | snp | A/G | 0.0115144 | 0.0749975 | utr-variant-3-prime | UBE2G1 | GRCh38.p7 | 17:4269288 | TGATGAGTGCTCTAT[A/G]AATCAATAAATGATG | 7326 |
rs13200 | snp | A/T | 0 | 0 | utr-variant-3-prime | UBE2G1 | GRCh38.p7 | 17:4272282 | ATATTATCCGGATCA[A/T]GTTGTGCTATGTACA | 7326 |
rs733622 | snp | A/G | 0.495135 | 0.0490805 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4277827 | CATGGTGATAAAGCC[A/G]TGAGAAAAGCCAGCC | 7326 |
rs747018 | snp | C/G | | | intron-variant | UBE2G1 | GRCh38.p7 | 17:4293496 | tgaacactcgtgttc[C/G]agtttttctggacat | 7326 |
rs893380 | snp | A/G | 0.487432 | 0.0782705 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4294739 | caacaacatggtgaa[A/G]ccccgtctttacaaa | 7326 |
rs893381 | snp | A/C | 0.0799831 | 0.183287 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4294933 | AATGGGAGAAACGTA[A/C]GTgagggagggaggg | 7326 |
rs934785 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4294069 | ATGTCATGAATTAAA[C/T]GAGTCCTCACAGCCT | 7326 |
rs986939 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4283770 | GGAGTTGGAGGAGAG[A/G]GGAAACAAAGGGAAA | 7326 |
rs1017445 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4316663 | TTTGTACCACGACAC[A/G]GGCTACCGGCTAGCT | 7326 |
rs1045734 | snp | G/T | 0 | 0 | utr-variant-3-prime | UBE2G1 | GRCh38.p7 | 17:4270114 | TCTACGGGAGTGGAA[G/T]TGAGAGCCAGGCATG | 7326 |
rs1045738 | snp | G/T | 0.487368 | 0.0784625 | utr-variant-3-prime | UBE2G1 | GRCh38.p7 | 17:4269648 | CCATATGAGGTTGAC[G/T]TGTCATACTAAGGTA | 7326 |
rs1113856 | snp | C/T | 0.166506 | 0.235645 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4343086 | GTTTTGCAGTTATTG[C/T]GGGAAGACAGATGGT | 7326 |
rs1113857 | snp | C/T | 0.0916144 | 0.193427 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4342692 | AGATGAGACATGATG[C/T]TAGCTTGGACCTGTA | 7326 |
rs1137718 | snp | A/G | 0 | 0 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4276431 | ggtgtcacgcctgta[A/G]tcccagcactttggg | 7326 |
rs1437808 | snp | C/T | 0.487049 | 0.0794222 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4272551 | ATTATATAGTCAATT[C/T]ATCAATTACAAAAGA | 7326 |
rs1806893 | snp | C/T | | | intron-variant | UBE2G1 | GRCh38.p7 | 17:4294431 | TCttttctttttttt[C/T]ttttttttttttttt | 7326 |
rs1806894 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4294145 | tataggcgtgagcca[C/T]gcgcctggtcTTAGA | 7326 |
rs1814417 | snp | A/T | 0.0799831 | 0.183287 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4294370 | GCAGTGAGCCAAGAT[A/T]GTCCCACTGCATTCC | 7326 |
rs1866174 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4302002 | TTGCTTACTTAGATG[C/T]GAGAGCAGAGAGAAT | 7326 |
rs1866175 | snp | A/C | 0.482234 | 0.0925596 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4302040 | AAAGAACAACAACAA[A/C]AAAAAAAGGGGGGGG | 7326 |
rs1866176 | snp | C/T | 0.494358 | 0.0528145 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4302150 | TGCCATGTTCCCTTT[C/T]ATTGGACTTGGGAAA | 7326 |
rs2004167 | snp | C/T | | | intron-variant | UBE2G1 | GRCh38.p7 | 17:4294324 | ggttcaaacgattct[C/T]ttgcctcagcctcct | 7326 |
rs2006746 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4283991 | TGAAACCCCATCTCA[A/T]CTAAAAGATACAAAA | 7326 |
rs2006757 | snp | C/T | 0.439085 | 0.163545 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4284029 | GGACGTGGTGGTGCA[C/T]GCCTGTAGTCCCAGC | 7326 |
rs2006762 | snp | C/G | 0.46974 | 0.119223 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4284104 | agacgttgcagtgag[C/G]caatatcgtgacact | 7326 |
rs2013273 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4277557 | ATCTCTATATAGGAC[A/G]AGGTATAAACACTAA | 7326 |
rs2013283 | snp | G/T | 0.102726 | 0.202016 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4277579 | AAACACTAACAAAAT[G/T]TGAGATAAAGCCTGG | 7326 |
rs2053255 | snp | A/G | 0.443195 | 0.158668 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4317941 | ACTTTGATCTCGCCT[A/G]TTTTATAGAAATAAA | 7326 |
rs2053258 | snp | C/T | 0.528624 | 0.111829 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4283360 | caaaaattagccagg[C/T]gtggtggcacatgcc | 7326 |
rs2304585 | snp | A/C | 0.153 | 0.230415 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4296967 | CAGTTACTTTCTCAA[A/C]TAAGTAGTTTAATAA | 7326 |
rs2325939 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4302997 | AAAACAGAAAAACAC[A/G]GGAGCTTCTTTTGAG | 7326 |
rs2325940 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4303374 | AATAAATAATAAAAC[C/T]GCAAAAGGGGAAAAA | 7326 |
rs2325941 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4303431 | AATAGAACATGGAAC[A/G]TTTGAAACATTTCCT | 7326 |
rs2325942 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4303455 | ATTTCCTAAGCATAG[A/G]GTTTTTACCCTAGAA | 7326 |
rs2325979 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4293867 | ACTATTCTTAGTTCA[A/C]GTTTTTATTGTTTTT | 7326 |
rs2325980 | snp | A/C | | | intron-variant | UBE2G1 | GRCh38.p7 | 17:4294430 | caaaaaaaaaaaaaa[A/C]aaaaaaaaaagaaag | 7326 |
rs2325981 | snp | A/G | | | intron-variant | UBE2G1 | GRCh38.p7 | 17:4294435 | aaaaaaaaaaaaaaa[A/G]aaaaagaaagaaacg | 7326 |
rs2325982 | snp | A/G | | | intron-variant | UBE2G1 | GRCh38.p7 | 17:4294440 | aaaaaaaaaaaaaaa[A/G]gaaagaaacgaaaag | 7326 |
rs2325983 | snp | A/C | 0.442655 | 0.159323 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4294449 | aaaaaaagaaagaaa[A/C]gaaaagaaaagaaaa | 7326 |
rs2325984 | snp | A/G | | | intron-variant | UBE2G1 | GRCh38.p7 | 17:4294455 | agaaagaaacgaaaa[A/G]aaaagaaaagaaaaa | 7326 |
rs2325985 | snp | A/G | | | intron-variant | UBE2G1 | GRCh38.p7 | 17:4294460 | gaaacgaaaagaaaa[A/G]aaaagaaaaaaaaGT | 7326 |
rs2325986 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4295935 | ACGTGCACAGCCATA[C/G]TAGATGCTTTCCAGG | 7326 |
rs2325987 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4295967 | TTAAAAAATGTAATA[C/T]GTTGTTTCATATGAC | 7326 |
rs2325988 | snp | A/G | 0.467337 | 0.123551 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4295989 | TCATATGACACTGCC[A/G]GTAATCTTACACCTA | 7326 |
rs2325989 | snp | A/G | 0.162253 | 0.234095 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4296025 | ACACATAGAAGAGTT[A/G]TCCATGGTATAAAAA | 7326 |
rs2875767 | snp | G/T | | | intron-variant | UBE2G1 | GRCh38.p7 | 17:4312715 | TTTTCTTGGCttttg[G/T]ttttttttttttttt | 7326 |
rs2875769 | snp | C/T | | | intron-variant | UBE2G1 | GRCh38.p7 | 17:4284843 | tcttttctttctttt[C/T]ttttttttttttttt | 7326 |
rs3169614 | snp | A/G | 0.00993419 | 0.0697739 | utr-variant-3-prime | UBE2G1 | GRCh38.p7 | 17:4270163 | AATGCAGTTAGTTTG[A/G]TAAAACCATGTGGGT | 7326 |
rs3859211 | snp | C/T | | | intron-variant | UBE2G1 | GRCh38.p7 | 17:4294441 | tcttttcgtttcttt[C/T]ttttttttttttttt | 7326 |
rs3902168 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4284473 | acagggattataggc[A/G]cgtgccaccatgcct | 7326 |
rs3966810 | snp | C/G | 0.454544 | 0.143743 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4346172 | TCTACCTTCTGAAAG[C/G]CTTTTACACTAATTA | 7326 |
rs4053438 | snp | C/T | 0.48 | 0.0979796 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4346434 | CATTTTCTTCTTCTT[C/T]TTTTTTTTTTTTTTT | 7326 |
rs4322703 | snp | C/T | 0.424659 | 0.17887 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4284645 | CTGCTAGTGTGGGTA[C/T]TGGTGCCAAAAACAA | 7326 |
rs4357975 | snp | C/T | 0.438246 | 0.16451 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4288493 | ggcctcccaaagtgc[C/T]gggattacagttgtg | 7326 |
rs4448984 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4295224 | AGCACAAGAGGCAAG[C/T]GTCACCCATTCATGC | 7326 |
rs4456561 | snp | C/T | 0.487933 | 0.0767327 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4321545 | TGGCCCAGGCTGGAG[C/T]GCAGTAGTGTGTTCA | 7326 |
rs4464134 | snp | A/G | 0.494272 | 0.053207 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4336880 | AAAATGGCTGAACAT[A/G]TGAAAGAATGAGATC | 7326 |
rs4467138 | snp | C/T | 0.439918 | 0.162576 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4321441 | CCCGTTTTTTTTACA[C/T]TGAGTGATTCTCTTT | 7326 |
rs4508454 | snp | A/G | 0.261332 | 0.249743 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4295355 | TCACTGCTGCCTTAG[A/G]TGCAATAAAATACGC | 7326 |
rs4790189 | snp | C/G | 0.0942527 | 0.195979 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4289900 | TACAATCATATAAAG[C/G]CAAAATTGTATTTTC | 7326 |
rs4790190 | snp | A/C | 0.0919752 | 0.193722 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4300937 | GACTCTGTTTTCAAA[A/C]AAAAAAAAAAGAGAG | 7326 |
rs4790191 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4301229 | TTCACTATTATTCTA[C/T]GATAGTCAGAATCAC | 7326 |
rs4790192 | snp | C/T | 0.211516 | 0.24702 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4308245 | GTAATCCCAGTTACT[C/T]GGGAGGCTGAGGCAG | 7326 |
rs4790602 | snp | G/T | 0.494526 | 0.0520291 | downstream-variant-500B | UBE2G1 | GRCh38.p7 | 17:4268822 | CTTTTGTCAGTAACT[G/T]ACTAAATGACCCCTG | 7326 |
rs4790603 | snp | C/T | 0.274661 | 0.248781 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4276000 | TTACCAAGCCAGTCT[C/T]TGTCTCTTCCTTCTG | 7326 |
rs4790604 | snp | A/C | 0.102726 | 0.202016 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4276935 | CAAGCCTTTGTACCA[A/C]CCCAACTCCACCCGT | 7326 |
rs4790605 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4297631 | CAAAAATACTAAATT[C/T]CTGTCTTGCGGCCTT | 7326 |
rs4790606 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4298134 | CATTTTTAAAAGCAG[C/G]TATTTCTAAAACAAG | 7326 |
rs4790607 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4300640 | ATCTTCATCACAGAT[A/G]CTATAGTATAAGTAC | 7326 |
rs4790608 | snp | A/C | 0.0919752 | 0.193722 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4308160 | AGAGTTTGAGACCAG[A/C]CTGACCAACATGGAG | 7326 |
rs4790609 | snp | A/G | 0.495708 | 0.0461266 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4308308 | TGGTGAGCCAAGATC[A/G]CGCCATTGCACTCCA | 7326 |
rs4790611 | snp | A/G | 0.120326 | 0.21374 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4322008 | GCCAAACAAGTCAGA[A/G]TGACAGCTTTGTCTA | 7326 |
rs4790612 | snp | A/C | 0.0755793 | 0.179102 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4324735 | TTAAATGATTTCTTG[A/C]GAAAATAATTAGAAA | 7326 |
rs4790613 | snp | A/C | 0.494774 | 0.0508504 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4328789 | TCTGTGCTGCACTAA[A/C]AACATGACAATGGTG | 7326 |
rs4790614 | snp | C/T | 0.495095 | 0.0492773 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4328911 | CTAACATGGTGAAAC[C/T]CCGTCTCTACTAAAA | 7326 |
rs5003078 | snp | C/T | | | intron-variant | UBE2G1 | GRCh38.p7 | 17:4284838 | TCTTTTCTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 7326 |
rs5818942 | in-del | -/A | 0.185472 | 0.241529 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4277792 | CATGACTGAAAACAC[-/A]AAAAAATACTCAGAA | 7326 |
rs5818947 | in-del | -/C | 0.417683 | 0.185425 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4303575 | CCCAAAGTCCATGTT[-/C]TTGAACACTACGTGA | 7326 |
rs5818953 | in-del | -/TTC | | | intron-variant | UBE2G1 | GRCh38.p7 | 17:4346422 | TATACAGCTTACATT[-/TTC]TTCTTCTTCTTTTTT | 7326 |
rs6502778 | snp | C/T | 0.470715 | 0.117409 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4327372 | agctacttgggaggc[C/T]gaggcaggagattcg | 7326 |
rs6502779 | snp | C/T | 0.494272 | 0.053207 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4335029 | AAATCTCaagAAAAT[C/T]ACATCGAGCACagca | 7326 |
rs6502780 | snp | A/G | 0.4941 | 0.0539917 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4341219 | ACAATTTCAGTCaac[A/G]cttactgggtactat | 7326 |
rs7207791 | snp | A/G | 0.388398 | 0.208197 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4337334 | TAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAGA | 7326 |
rs7208636 | snp | C/T | | | intron-variant | UBE2G1 | GRCh38.p7 | 17:4284820 | ttctttttctttttc[C/T]tttcttttcttttct | 7326 |
rs7211833 | snp | C/T | 0.455621 | 0.142197 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4361940 | gcaatccagcctggg[C/T]gacagagcaagactg | 7326 |
rs7212235 | snp | A/G | 0.0908922 | 0.192833 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4299197 | ATATGTATGCACTGC[A/G]TCATGATGTAAAGTA | 7326 |
rs7214726 | snp | A/G | 0.150667 | 0.229419 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4347617 | atagctgcaactaca[A/G]gcaaatgccaccatg | 7326 |
rs7214808 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4308468 | aggcaaatgttgcat[C/T]aagccaagatcacgc | 7326 |
rs7214818 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4326050 | aatcttcaagacatt[G/T]gatttagcaacaaac | 7326 |
rs7215376 | snp | A/G | 0.13446 | 0.221699 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4308469 | ggcaaatgttgcatc[A/G]agccaagatcacgcc | 7326 |
rs7216130 | snp | A/T | 0.417683 | 0.185425 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4303948 | AAAGAGAGATAAAAG[A/T]TATACAGTCATCATT | 7326 |
rs7216966 | snp | C/T | 0.422 | 0.181428 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4274354 | AGGCGCCTGCCACCA[C/T]GCCCGGCTAATTTTT | 7326 |
rs7218234 | snp | C/T | 0.135825 | 0.222405 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4299220 | GTAAAGTATTTCTAA[C/T]TATGGGTTTGAAAGC | 7326 |
rs7218432 | snp | C/T | 0.135825 | 0.222405 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4299393 | gccagagtgagactc[C/T]gtctcaacaacaaca | 7326 |
rs7219326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4302316 | GTTCTGCGTGTGGTT[A/G]CAGCCACTCTTGTGT | 7326 |
rs7219610 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4310935 | AATGACATGagctgg[A/G]catggtggctcaccg | 7326 |
rs7219792 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4311066 | aaaaaagaaacaaaa[A/G]agtacaaaaattagc | 7326 |
rs7220341 | snp | A/G | 0.0908922 | 0.192833 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4311410 | aaggcagaaactcaa[A/G]tgtccatcgacaaat | 7326 |
rs7221389 | snp | A/C | | | intron-variant | UBE2G1 | GRCh38.p7 | 17:4279663 | gcccgtaatcccagc[A/C]ctctgggacgctgag | 7326 |
rs7221915 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | UBE2G1 | GRCh38.p7 | 17:4311264 | aaaaaaagtaAAAtg[A/G]catatgattaaaaag | 7326 |