SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs701537 | snp | A/T | 0.474992 | 0.108989 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386017 | TGAAATGGGATGGAG[A/T]AGAACAACAGCAGGC | 337867 |
rs723090 | snp | C/T | 0.431916 | 0.171483 | intron-variant | UBAC2 | GRCh38.p7 | 13:99364851 | CAAATGCCCATCAAC[C/T]ATAGAATGGGTAAGT | 337867 |
rs727263 | snp | A/G | 0.299267 | 0.245097 | intron-variant, nc-transcript-variant | UBAC2, FKSG29 | GRCh38.p7 | 13:99351854 | TGCCCGGTGTTAACT[A/G]GTTGATTATCACCTC | 337867 |
rs731150 | snp | A/G | 0.308414 | 0.24308 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99355296 | ATTTCTGCATCGTAT[A/G]TTCTGTTTTCCCTTC | 337867 |
rs731955 | snp | A/T | 0.462472 | 0.13174 | intron-variant | UBAC2 | GRCh38.p7 | 13:99218386 | TGAGCTGTAAAATTT[A/T]AAATCCTAGTCCTGA | 337867 |
rs747847 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383679 | TTCCGGGGAGGAGCA[C/T]GCTCACTGCGTGCAT | 337867 |
rs747848 | snp | C/T | 0.421684 | 0.181726 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383928 | GCACCTTCTTCCTCA[C/T]CTTGCTGAGTCCTTA | 337867 |
rs752820 | snp | C/T | 0.311859 | 0.242226 | intron-variant | UBAC2 | GRCh38.p7 | 13:99217858 | GGTGGCAGCGTCCAC[C/T]GAGCTCGTGCCCACC | 337867 |
rs877856 | snp | C/T | 0.431916 | 0.171483 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341776 | CATTCTGATTTCTCA[C/T]ACCTTTCGCTCTTCT | 337867 |
rs912129 | snp | C/T | 0.393434 | 0.20476 | intron-variant | UBAC2 | GRCh38.p7 | 13:99381398 | CACAAACGAATCCAT[C/T]TGCTGTCCACACTCA | 337867 |
rs912130 | snp | A/C | 0.498547 | 0.0269177 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380148 | tggcagtacaaatgg[A/C]aagttccacacctga | 337867 |
rs912131 | snp | C/T | 0.496314 | 0.0427728 | intron-variant | UBAC2 | GRCh38.p7 | 13:99380092 | atgcaggccacaaca[C/T]gtagtttattcagtg | 337867 |
rs913464 | snp | A/G | 0.362523 | 0.223246 | intron-variant | UBAC2 | GRCh38.p7 | 13:99337735 | GGCCTTGGCCTTCCC[A/G]ACCCACATGGACCCT | 337867 |
rs927988 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | UBAC2 | GRCh38.p7 | 13:99333024 | CCCAGCACTTGGGGA[A/G]GCCAAGATGGGAAGA | 337867 |
rs927989 | snp | C/G | 0.498503 | 0.0273153 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335452 | ACAGAGAATGCCTCT[C/G]CCTACCCCCTACCCT | 337867 |
rs984477 | snp | C/G | 0.495818 | 0.0455352 | intron-variant | UBAC2 | GRCh38.p7 | 13:99220179 | TATAAAGTTATCATA[C/G]TTCCTTCTTATATAT | 337867 |
rs1042263 | snp | C/G/T | 3.33611e-05 | 0.00408405 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295900 | TATACTTTTTACCAC[C/G/T]GCTTTGCCTACACGA | 337867 |
rs1042273 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294936 | TTTCTTTCATTGGGC[A/G]CTTTCCCATCTCCAA | 337867 |
rs1051577 | snp | A/C | 0.0089417 | 0.0662638 | missense, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255044 | ACCTTCCTCATGAAC[A/C]TCAGCACGTGTCTGG | 337867 |
rs1058083 | snp | A/G | 0.475259 | 0.108435 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385979 | TTGCTCAGAGTATCC[A/G]GAGTTAGCCACTAGG | 337867 |
rs1058143 | snp | C/T | 0.474544 | 0.10991 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99386082 | GTGGCTGGCCTGGCA[C/T]GGGCTCAGCCCAGGA | 337867 |
rs1060436 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335697 | CTGTGTTGTATGAAT[A/G]ACCCACTCTGCAGCT | 337867 |
rs1060437 | snp | G/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335782 | GCAGTGGAATGAGCC[G/T]CAAAGCTCTACTTGG | 337867 |
rs1060438 | snp | A/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335785 | GTGGAATGAGCCTCA[A/T]AGCTCTACTTGGTGT | 337867 |
rs1060440 | snp | A/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99335786 | TGGAATGAGCCTCAA[A/T]GCTCTACTTGGTGTT | 337867 |
rs1134061 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | UBAC2 | GRCh38.p7 | 13:99325303 | AGAGACGGGGTTTCA[C/T]CGTGTTAGGCAGGAT | 337867 |
rs1160294 | snp | C/T | 0.498158 | 0.0302955 | intron-variant | UBAC2 | GRCh38.p7 | 13:99281340 | AATGGATTATATGCT[C/T]CTCTCTTAGGTAAGA | 337867 |
rs1319132 | snp | C/G | 0.498813 | 0.0243321 | intron-variant | UBAC2 | GRCh38.p7 | 13:99347347 | TATCATCTTCACTTG[C/G]CTTTTTTTTCCTGGG | 337867 |
rs1887701 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99259774 | CATAGCTTAGGACTT[C/T]TCTAAAATTAAGTAT | 337867 |
rs1887702 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | UBAC2 | GRCh38.p7 | 13:99292569 | GAAAGGAAGATGTTA[C/T]ATAATATATGGACTG | 337867 |
rs1887703 | snp | C/T | 0.308166 | 0.243139 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99297729 | GGTAAGTAGAAAACA[C/T]AAGAGGGTAGGGATG | 337867 |
rs1887704 | snp | C/G | 0.494315 | 0.0530107 | intron-variant | UBAC2 | GRCh38.p7 | 13:99322238 | AATTCCACTAATTTT[C/G]TTACACATTAATACT | 337867 |
rs1923891 | snp | C/T | 0.119281 | 0.213102 | intron-variant, upstream-variant-2KB | UBAC2, GPR183 | GRCh38.p7 | 13:99307691 | TAAGGTTTATTGCTT[C/T]AGTCTCTTTCAAAGA | 337867 |
rs1923894 | snp | A/G | 0.265453 | 0.249522 | intron-variant | UBAC2 | GRCh38.p7 | 13:99370504 | CAATTTGTTTTGTTT[A/G]CTGAAAGGGAAAAAC | 337867 |
rs1923895 | snp | C/T | 0.498437 | 0.0279115 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366338 | ctcagaattcaaaac[C/T]acaaaatccacaagg | 337867 |
rs1923896 | snp | C/T | 0.322245 | 0.239334 | intron-variant | UBAC2 | GRCh38.p7 | 13:99366033 | aaatcagagaaatac[C/T]aatcaaagaaagctg | 337867 |
rs1923897 | snp | A/G | 0.487368 | 0.0784625 | intron-variant, downstream-variant-500B | UBAC2, FKSG29 | GRCh38.p7 | 13:99352087 | CATGATTGACAGGGC[A/G]GATCTGCCTCCTGGT | 337867 |
rs1927565 | snp | A/G | 0.49823 | 0.0296997 | upstream-variant-2KB, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99198781 | TTTATGGTTCAAATT[A/G]ATCTTTTACCCACAT | 337867 |
rs1927724 | snp | A/C | 0.42357 | 0.179927 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340058 | ACAATCTTTTACCAG[A/C]ACTTTGAATACTAAA | 337867 |
rs1927725 | snp | C/T | 0.309154 | 0.242901 | intron-variant | UBAC2 | GRCh38.p7 | 13:99340233 | AAATACCGTGTGCAG[C/T]GTCTGGAGGCTGCTG | 337867 |
rs1927726 | snp | A/G | 0.357238 | 0.225832 | intron-variant | UBAC2, GPR18 | GRCh38.p7 | 13:99260629 | AAAAGAAACTGCCCA[A/G]TCATTTGACAGCAAG | 337867 |
rs1927727 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99302910 | CTTTGAGTCCTAAAT[C/T]GATAGCTATGTTTAT | 337867 |
rs1927728 | snp | C/T | 0.304937 | 0.243889 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303279 | GCTTTATATGTGTCC[C/T]GAACCCAGTGGATGT | 337867 |
rs1927729 | snp | A/G | 0.223522 | 0.248594 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99303544 | GAAACTAAGAATCCC[A/G]CCATAATACTCATTT | 337867 |
rs1927730 | snp | C/T | 0.308908 | 0.242961 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99306311 | GTTTTTTAGCACTTA[C/T]AATGAGAGGCAATGT | 337867 |
rs1927731 | snp | A/G | 0.42263 | 0.180829 | intron-variant | UBAC2 | GRCh38.p7 | 13:99273618 | CTGTTGATGAATTTA[A/G]TGTTGATCTGATTAT | 337867 |
rs1927732 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | UBAC2 | GRCh38.p7 | 13:99226485 | AGCCTTCTAACTGGT[A/T]TACTATCTTCCACCA | 337867 |
rs1964897 | snp | A/G | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344929 | TGCTCATCTATTTCA[A/G]CTACAACTGCCTGAG | 337867 |
rs1964898 | snp | C/T | 0.422787 | 0.180679 | intron-variant | UBAC2 | GRCh38.p7 | 13:99344927 | CTCATCTATTTCAGC[C/T]ACAACTGCCTGAGCT | 337867 |
rs1977252 | snp | A/C | 0.247053 | 0.249983 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382337 | ACATAAAATGCTGTC[A/C]AGTCAGGTCTCTCAA | 337867 |
rs1977253 | snp | C/T | 0.378174 | 0.214642 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382274 | catatctctgttaaa[C/T]tccatctgatcattt | 337867 |
rs1977254 | snp | C/G | 0.375996 | 0.215928 | intron-variant | UBAC2 | GRCh38.p7 | 13:99382266 | tgttaaattccatct[C/G]atcattttccagtca | 337867 |
rs1998475 | snp | C/T | 0.349671 | 0.229272 | intron-variant | UBAC2 | GRCh38.p7 | 13:99312121 | AACCAAACCAAAATA[C/T]AACACACACAAAACA | 337867 |
rs2004229 | snp | A/G | 0.305685 | 0.24372 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338300 | GAGGCCAAGGCGGGC[A/G]GATCACAAGAGGTCA | 337867 |
rs2038673 | snp | A/T | 0.0611083 | 0.163768 | intron-variant | UBAC2 | GRCh38.p7 | 13:99365139 | ATAATGGCAGATTTT[A/T]AAAAAATCACAAGAA | 337867 |
rs2093642 | snp | A/G | 0.306431 | 0.243548 | intron-variant | UBAC2 | GRCh38.p7 | 13:99379376 | ggtgagtttgccaag[A/G]tcattgctgacaaaa | 337867 |
rs2146676 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99368852 | gaatccaccgttttc[C/T]taaataggcctggtt | 337867 |
rs2146677 | snp | A/T | 0.308908 | 0.242961 | intron-variant | UBAC2 | GRCh38.p7 | 13:99359417 | TTTACTTGAATGAGT[A/T]AATGTAAAATCACAA | 337867 |
rs2146678 | snp | A/T | 0.307671 | 0.243257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331755 | TTTGTACATTCCCTA[A/T]TTTATTACCCCAAGA | 337867 |
rs2149261 | snp | C/T | 0.498253 | 0.0295011 | intron-variant | UBAC2 | GRCh38.p7 | 13:99277844 | ATCAAGCCTCTAATC[C/T]GGAGGTGGGTGGTGG | 337867 |
rs2149262 | snp | C/G | 0.445064 | 0.156365 | intron-variant | UBAC2 | GRCh38.p7 | 13:99288417 | TAGCATGCAGATAGA[C/G]AACAGCTTTAAAATT | 337867 |
rs2149263 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | UBAC2, GPR183 | GRCh38.p7 | 13:99299696 | CTTTTCAAAGCTTGC[C/T]GTTCAGTGTTCCTTT | 337867 |
rs2149264 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | UBAC2 | GRCh38.p7 | 13:99214730 | TCCTTAAGCAGATTG[C/T]CCCCCACCCCACCCT | 337867 |
rs2181500 | snp | C/T | 0.0295035 | 0.117819 | intron-variant, upstream-variant-2KB | UBAC2, FKSG29 | GRCh38.p7 | 13:99350540 | ccctgctccagcaca[C/T]attcagcaatctgga | 337867 |
rs2181501 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331103 | GAAGGATAAGAGATA[C/T]GTGATCTCAGCTGGA | 337867 |
rs2181502 | snp | C/T | 0.498059 | 0.0310896 | intron-variant | UBAC2 | GRCh38.p7 | 13:99331065 | CTGGCTCAAATAAAA[C/T]GAACCTTCCCTTATG | 337867 |
rs2182885 | snp | A/G | 0.454784 | 0.1434 | intron-variant | UBAC2 | GRCh38.p7 | 13:99202870 | GGTGCTGGGAATGCA[A/G]CAACGAACAGGTCCT | 337867 |
rs2182886 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | UBAC2 | GRCh38.p7 | 13:99215020 | GGGATATGACCTTTA[C/T]TGAGCTTATCCACCA | 337867 |
rs2182954 | snp | C/T | 0.445724 | 0.155538 | intron-variant | UBAC2 | GRCh38.p7 | 13:99284828 | CATATTCTAAGGCTG[C/T]TGGAAAATTAAAGTT | 337867 |
rs2225170 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | UBAC2 | GRCh38.p7 | 13:99219708 | atccctgtattaagc[A/C]gtcatgccctattac | 337867 |
rs2230341 | snp | A/G | 0.311859 | 0.242226 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99295007 | ATGACAAACTTTGCA[A/G]GACTTCCCTTATAAA | 337867 |
rs2230342 | snp | G/T | 0.426238 | 0.177314 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295924 | TTCAACAAATTTGGT[G/T]ATTTCTGATATACTT | 337867 |
rs2230343 | snp | C/T | 0.112385 | 0.208715 | intron-variant, synonymous-codon | UBAC2, GPR183 | GRCh38.p7 | 13:99295843 | CTGGAGAATCGGAGA[C/T]GCCTTGTGTAGGATA | 337867 |
rs2296044 | snp | A/G | 0.41325 | 0.18934 | downstream-variant-500B | UBAC2 | GRCh38.p7 | 13:99386571 | GTGCTACTTACAGGA[A/G]CAAAAGCACTTCACT | 337867 |
rs2296045 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385778 | AGTTTGAGAGAAAAA[A/G]CAGTAACTAAAAAAG | 337867 |
rs2296046 | snp | C/T | 0.371785 | 0.218331 | intron-variant | UBAC2 | GRCh38.p7 | 13:99372616 | CTTTAGACTCAGAGC[C/T]GGTGACGCCACCTGT | 337867 |
rs2296860 | snp | A/G | 0.49823 | 0.0296997 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | UBAC2, UBAC2-AS1 | GRCh38.p7 | 13:99200499 | TCGGGAGAGATTAGA[A/G]GTGGCGCTCCTGCCC | 337867 |
rs2296911 | snp | A/G | 0.498323 | 0.0289051 | intron-variant | UBAC2 | GRCh38.p7 | 13:99240059 | TGTGGTACAGGAAGC[A/G]TGCTTTGAGGCAAAC | 337867 |
rs2390236 | snp | A/T | 0.0607341 | 0.163335 | intron-variant | UBAC2 | GRCh38.p7 | 13:99236666 | accagcctggccaac[A/T]tggtgaaaccccgtc | 337867 |
rs2390237 | snp | C/G | 0.470521 | 0.117772 | intron-variant | UBAC2 | GRCh38.p7 | 13:99336050 | GAGCTTTACATTTTT[C/G]CCAGTTGCTGTATTT | 337867 |
rs2390238 | snp | C/T | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99338047 | TTTTTTTCTTTTTTT[C/T]TTTTTTTTTTTTTTT | 337867 |
rs2390239 | snp | G/T | 0.305685 | 0.24372 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341466 | GCAGAGTCTACAAGA[G/T]AAATAGAGAAGCAAA | 337867 |
rs2390240 | snp | A/T | 0.15698 | 0.23205 | intron-variant | UBAC2 | GRCh38.p7 | 13:99345981 | CCCCTGACCTCATGA[A/T]CCACTTGCCTTGGCC | 337867 |
rs2390241 | snp | C/G | 0.00475057 | 0.0485048 | intron-variant, upstream-variant-2KB | UBAC2, MIR623 | GRCh38.p7 | 13:99354481 | CTGTTCACTTGGCGG[C/G]TTGGCTGAGTTCTGT | 337867 |
rs2390276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC2 | GRCh38.p7 | 13:99383519 | TGAATCACCTGAGGG[C/T]GCCATAGTGTCCCAG | 337867 |
rs2892975 | snp | C/T | 0.308661 | 0.24302 | intron-variant | UBAC2 | GRCh38.p7 | 13:99373549 | CGGAATGTCCTGCCC[C/T]GAGGAGCTGTGAGCC | 337867 |
rs3031384 | in-del | -/GT | 0 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216113 | TGTGTGTGTGTGTGT[-/GT]ATTTTTGAGACACAG | 337867 |
rs3031409 | in-del | -/A/AA | 0 | 0 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99256723 | CCAAAAAAAAAAAAA[-/A/AA]CCGTCCATTTTAAAT | 337867 |
rs3031412 | in-del | -/T/TT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99292729 | AGGGTTTTTTTTTTT[-/T/TT]AATGTGGTCAACTGC | 337867 |
rs3031415 | in-del | -/A/AA | 0.5 | 0 | intron-variant | UBAC2 | GRCh38.p7 | 13:99341032 | GTAGATAAAAAAAAA[-/A/AA]TGCTGTGTTTTCTCA | 337867 |
rs3031440 | in-del | -/TGTGTGT | | | intron-variant | UBAC2 | GRCh38.p7 | 13:99368720 | gtgtgtgtgtgtgtg[-/TGTGTGT]acacataccctcact | 337867 |
rs3181718 | snp | A/G | 0.201727 | 0.245295 | intron-variant, utr-variant-3-prime | UBAC2, GPR183 | GRCh38.p7 | 13:99294599 | GTTTTGTTTTGTTTC[A/G]TTCTGGGTCATAAAA | 337867 |
rs3223410 | microsatellite | (CA)11/13/14/15/16/17/19 | 0.746112 | 0.121802 | intron-variant | UBAC2 | GRCh38.p7 | 13:99216111 | tgtgtctcaaaaata[(CA)11/13/14/15/16/17/19]aaaTAtaggttggta | 337867 |
rs3742127 | snp | C/T | 0.164546 | 0.234942 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99327198 | TTTTCTCTGAATGTT[C/T]CTTTACTTCAGATTG | 337867 |
rs3742130 | snp | C/T | 0.275128 | 0.248734 | synonymous-codon, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99255087 | GGGAACGGGGGAGAA[C/T]AGTTACAATCCCTGG | 337867 |
rs3759443 | snp | C/T | 0.165527 | 0.235296 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258068 | ATTTCATTTTAATAA[C/T]ACAGGCTGGGCGCAA | 337867 |
rs3759444 | snp | A/G | 0.320575 | 0.239832 | intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99258009 | GGGAGGCCAAGGCAG[A/G]AGGATCAGTTGTGCC | 337867 |
rs3809367 | snp | A/G | 0.164546 | 0.234942 | upstream-variant-2KB, intron-variant | GPR18, UBAC2 | GRCh38.p7 | 13:99260280 | TTGCATTGTTACTGC[A/G]TATTTACTTGCTTTT | 337867 |
rs3825426 | snp | C/G | 0.360421 | 0.224293 | intron-variant, utr-variant-5-prime | UBAC2 | GRCh38.p7 | 13:99326818 | ACTTTAAGAATAACT[C/G]TGTCTGTGCATCTCG | 337867 |
rs3839999 | in-del | -/T | 0.229136 | 0.249128 | utr-variant-3-prime, nc-transcript-variant | UBAC2 | GRCh38.p7 | 13:99385549 | TATTTTCTATCTATA[-/T]TTTTTATTGGGCATT | 337867 |