SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6173905 | snp | A/C | 0.5 | 0 | intron-variant | Wdr92 | Mm_Celera | 11:17223214 | agggtgtttgatgcc[A/C]cagtgtaggggaatg | 103784 |
rs6174424 | snp | A/G | 0.5 | 0 | intron-variant | Wdr92 | Mm_Celera | 11:17223267 | ggtgggtgggtgggt[A/G]agggagcaccctcac | 103784 |
rs6175020 | snp | A/G | 0.5 | 0 | intron-variant | Wdr92 | Mm_Celera | 11:17223403 | aaaCAAAAGAAAAAA[A/G]AATGTATTTCTAAAT | 103784 |
rs13461291 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon, upstream-variant-2KB | Pno1, Wdr92 | GRCm38.p3 | 11:17211487 | GACGCAAAGCACCGG[A/G]ACGGAGGACGGCTTT | 103784 |
rs26851144 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Wdr92 | Mm_Celera | 11:17234987 | GTTCTTATCAGCTAG[C/T]ATTTGGTTTGTACTA | 103784 |
rs26851145 | snp | G/T | 0.32 | 0.24 | utr-variant-3-prime | Wdr92 | Mm_Celera | 11:17234972 | ACGTTGCTGCCGTGC[G/T]TTCTTATCAGCTAGT | 103784 |
rs26851146 | snp | A/T | 0.231111 | 0.249285 | utr-variant-3-prime | Wdr92 | Mm_Celera | 11:17233922 | TTAATCATACCTGCA[A/T]TAAACCTTGTGTCTC | 103784 |
rs26851147 | snp | A/C | 0.231111 | 0.249285 | utr-variant-3-prime | Wdr92 | Mm_Celera | 11:17233721 | GTAAGTGATGACGAG[A/C]CGTTGAAGATTGAAT | 103784 |
rs26851148 | snp | C/G | 0.231111 | 0.249285 | utr-variant-3-prime | Wdr92 | Mm_Celera | 11:17233701 | TTAGTTGTCTTTTGA[C/G]TGTGGTAAGTGATGA | 103784 |
rs26851149 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Wdr92 | Mm_Celera | 11:17233641 | CAGTGTAACTGGTAA[A/G]ATACTGTGACTTCCA | 103784 |
rs26851150 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime | Wdr92 | Mm_Celera | 11:17233568 | GAGTCACTTCACTTG[C/G]TCTGTAAAGCTCCAG | 103784 |
rs26851151 | snp | G/T | 0.244898 | 0.249948 | utr-variant-3-prime | Wdr92 | Mm_Celera | 11:17233469 | AATGTAAAGCCAAAG[G/T]CAGTAGTTGTTATTT | 103784 |
rs26851152 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime | Wdr92 | Mm_Celera | 11:17233166 | TTTCTACTCAGAAAC[A/G]TTAGGGCCAGGAGTT | 103784 |
rs26851153 | snp | A/T | 0.231111 | 0.249285 | utr-variant-3-prime | Wdr92 | Mm_Celera | 11:17232925 | TTTGACTCAGACTTT[A/T]CACTTGACATTGTCC | 103784 |
rs26851154 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Wdr92 | Mm_Celera | 11:17232713 | GTCTTTTAGTGAATA[C/T]CCAACTCAGCGGTCA | 103784 |
rs26851155 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr92 | Mm_Celera | 11:17232549 | TCACCGTTGCCCGAG[A/G]ATGAAATTCTGCCTT | 103784 |
rs26851156 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr92 | Mm_Celera | 11:17232545 | AAAGTCACCGTTGCC[C/T]GAGGATGAAATTCTG | 103784 |
rs26851157 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdr92 | Mm_Celera | 11:17232411 | GGCCATCCAAATTTC[A/G]GAAAGAATTACAACA | 103784 |
rs26851158 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr92 | Mm_Celera | 11:17232355 | TTTGTAACTGTTGCT[C/T]ACAGCCCTTTCTGTG | 103784 |
rs26851159 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Wdr92 | Mm_Celera | 11:17231949 | TTTGTTGCTTGGTTG[A/C]TTGCAGTGTTTTTGC | 103784 |
rs26851160 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr92 | Mm_Celera | 11:17231764 | AAGTATCAGATATGT[A/G]CCACTGCATGCGAGA | 103784 |
rs26851161 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr92 | Mm_Celera | 11:17231452 | TGAAATAGAGTGCAC[C/T]TGAGCTTGGATTGTG | 103784 |
rs26851162 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17231416 | TTTGCGGGGAAGCTT[G/T]TGCCAGCAGAGAGAA | 103784 |
rs26851163 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Wdr92 | Mm_Celera | 11:17230890 | TTGATTCCCCATTTC[G/T]TGAGACTGCTTCCAC | 103784 |
rs26851164 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17230533 | GAGAACTGGAGCTAT[A/G]TTAACTGACAAACTT | 103784 |
rs26851165 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr92 | Mm_Celera | 11:17230464 | AGTTTACAAAGCCTT[C/T]CCTAAGCTCCTGTTA | 103784 |
rs26851166 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Wdr92 | Mm_Celera | 11:17230335 | TTTAAACAAATTGAA[A/T]GTTTGAAAACGTTAA | 103784 |
rs26851167 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr92 | Mm_Celera | 11:17229987 | TCTAGGTGTTATGTA[A/G]CTAGTTTTCAAAATA | 103784 |
rs26851168 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17229763 | CATGTGTGTATGTCT[A/G]ACTAGGCCCATAAAT | 103784 |
rs26851169 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17229725 | GAGTCTACTCTTCAG[A/G]GCTTCCATTTAGTCT | 103784 |
rs26851170 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdr92 | Mm_Celera | 11:17229585 | TTTGAGTCAGGAAGG[C/T]GCCAACAGGCCCCAC | 103784 |
rs26851171 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17229459 | AGTCTAGAAAAGCCA[C/T]GCCCGGGCATATCTC | 103784 |
rs26851172 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr92 | Mm_Celera | 11:17228830 | ACAAAAGATGTCTGG[A/G]ATAAAGTACATATAA | 103784 |
rs26851173 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17228684 | CTGGATTAGAAAGTG[A/G]GAGATATCCAGCAAT | 103784 |
rs26851174 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17228663 | AAGTGAACTTGCTTT[A/G]GAACACTGGATTAGA | 103784 |
rs26851175 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17228381 | GTACTTGTGGGATCT[G/T]AAGTGGTTTGTGTAG | 103784 |
rs26851176 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17227580 | CCTCCTGCCCTTCTG[A/T]GGACCAGCGGATGAT | 103784 |
rs26851177 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Wdr92 | Mm_Celera | 11:17227315 | CCAACATCACTGAGC[A/G]TGTTTGTACCTGCTC | 103784 |
rs26851178 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17226970 | TCTGTTTAGAATCCA[C/G]TGAACACTTTCAAGT | 103784 |
rs26851179 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17226647 | ACCGTCCCGGAGTTA[A/C]GCATGCTGAAATTAA | 103784 |
rs26851180 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17226481 | CCATCAAGAGCGCAC[A/G]GTAGAAATGCAAGCC | 103784 |
rs26851181 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17226450 | GCTTGGGACCTAGAA[A/G]AGCAAGATATTGGTA | 103784 |
rs26851182 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17226383 | AATGGAGAGAAAGAC[A/G]TTGTTCATTGAAAAG | 103784 |
rs26851183 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17225757 | GGGCACCTCCATGGC[C/T]GCCCAACTTTGGATT | 103784 |
rs26851184 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr92 | Mm_Celera | 11:17224882 | TAATAGTGTTGAGGA[A/G]CCAATGAAGTAATGT | 103784 |
rs26851185 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17224530 | TATGAATTTTGCCAA[C/T]GCCTTTTATCTATGA | 103784 |
rs26851186 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17224261 | TTGTATGTATGTGGT[A/G]CTAACCCAGACAATA | 103784 |
rs26851187 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr92 | Mm_Celera | 11:17223817 | GTTCACATGTAGGCC[A/G]TTTAGCCATCTCAGT | 103784 |
rs26851188 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17223039 | CTTTAGCTTAATGGC[C/T]GTAACATTCCATCGT | 103784 |
rs26851189 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17222001 | TGTGTTTTCCTCTAG[C/T]GTTTTCAGAGCCTCT | 103784 |
rs26851190 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr92 | Mm_Celera | 11:17221396 | AGCCAAGCGTTCATA[A/G]CCACGTCACTTTATC | 103784 |
rs26851191 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17221235 | TAAGAGGAAACATGA[C/T]TCCTTTTTTCCCCTG | 103784 |
rs26851192 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wdr92 | Mm_Celera | 11:17220879 | GAAATTATTTTCACA[C/T]TTTATTCCATGTGTG | 103784 |
rs26851193 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Wdr92 | Mm_Celera | 11:17220361 | ATTCATCATTTTACA[G/T]ATTTTGTCGTAGAGC | 103784 |
rs26851194 | snp | A/T | 0.32 | 0.24 | intron-variant | Wdr92 | Mm_Celera | 11:17219469 | AAAGGACAAAGGTTT[A/T]AAAAGATGGTTTTTG | 103784 |
rs26851195 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Wdr92 | Mm_Celera | 11:17219378 | ATGAACAAACATGCC[A/G]ACTGTGAAAGAGTAA | 103784 |
rs26851196 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Wdr92 | Mm_Celera | 11:17218500 | GTAATCACATGGTCT[C/T]TCAGTTTTAGACCAG | 103784 |
rs26851197 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Wdr92 | Mm_Celera | 11:17218275 | GTACCAACCTGGCAC[C/T]AGCAGAGATGGGAGA | 103784 |
rs26851198 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr92 | Mm_Celera | 11:17218164 | CACTGAACACCAACC[A/G]GATTCTGTAGCTAGG | 103784 |
rs26851199 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Wdr92 | Mm_Celera | 11:17216699 | GTCAGCTTAGCTCAG[C/T]GCCAGGATTCACTAA | 103784 |
rs26851200 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Wdr92 | Mm_Celera | 11:17216281 | AAGTGAGGTTAAAAC[G/T]AAAAGGCAAATTAGC | 103784 |
rs26851201 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Wdr92 | Mm_Celera | 11:17214933 | GAAGGTTGGGCACTT[C/T]GGCATACACCTTTAA | 103784 |
rs26851202 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Wdr92 | Mm_Celera | 11:17214811 | CCTGTCTCAAAGGCT[G/T]GCTCCAAACCCTATG | 103784 |
rs26851203 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Wdr92 | Mm_Celera | 11:17214314 | TTCAATAGAAAAGCA[C/T]GTGGGTTAAATCGAT | 103784 |
rs26851204 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Wdr92 | Mm_Celera | 11:17213940 | GAATAGGCTTGTGGT[C/G]TTTTGCTTTCCCAAG | 103784 |
rs26851205 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Wdr92 | Mm_Celera | 11:17213832 | AGTCAGTGTGTGGGG[A/T]AAGGACTCTGAACAC | 103784 |
rs26851206 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Wdr92 | Mm_Celera | 11:17213685 | GTCTCATTTCTAGAT[A/T]GTAAGCTGGAGAGCA | 103784 |
rs26851207 | snp | G/T | 0.260355 | 0.249785 | upstream-variant-2KB, intron-variant | Pno1, Wdr92 | Mm_Celera | 11:17213455 | GAGAGCCTGTTTTCC[G/T]GTTTAGTTCCTACTC | 103784 |
rs26851208 | snp | G/T | 0.493827 | 0.0552116 | upstream-variant-2KB, intron-variant | Pno1, Wdr92 | Mm_Celera | 11:17213395 | GAGGATAGATAAGCT[G/T]GCAGGGCAAGGTATG | 103784 |
rs26851209 | snp | A/C/T | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Pno1, Wdr92 | GRCm38.p3 | 11:17213342 | CAAATTGCAGCCACA[A/C/T]GGAGGTGTTGAGAGC | 103784 |
rs26851210 | snp | C/T | 0.260355 | 0.249785 | upstream-variant-2KB, intron-variant | Pno1, Wdr92 | GRCm38.p3 | 11:17213204 | CCTCAAACTGATAAT[C/T]CTCAAACAAGGCTCT | 103784 |
rs26851211 | snp | A/G | 0.277778 | 0.248452 | upstream-variant-2KB, intron-variant | Pno1, Wdr92 | GRCm38.p3 | 11:17213059 | TAGATTACAGGTTTC[A/G]TATCCAGCTGCCAGT | 103784 |
rs26851212 | snp | C/T | 0.396694 | 0.202437 | upstream-variant-2KB, intron-variant | Pno1, Wdr92 | GRCm38.p3 | 11:17213044 | CGGATAATGCAAGAC[C/T]AGATTACAGGTTTCG | 103784 |
rs26851213 | snp | C/T | 0.396694 | 0.202437 | upstream-variant-2KB, intron-variant | Pno1, Wdr92 | Mm_Celera | 11:17212968 | GATATGTAAGACATT[C/T]CACAGATTTGTCCTT | 103784 |
rs26851214 | snp | A/G | 0.297521 | 0.245442 | upstream-variant-2KB, intron-variant | Pno1, Wdr92 | Mm_Celera | 11:17212879 | TCAGTTTGAAACCCT[A/G]TCTGCAACAACCACA | 103784 |
rs26851215 | snp | G/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Pno1, Wdr92 | Mm_Celera | 11:17212863 | AAACAGCAGGAGAAT[G/T]TCAGTTTGAAACCCT | 103784 |
rs26851216 | snp | C/T | 0.18 | 0.24 | upstream-variant-2KB, intron-variant | Pno1, Wdr92 | Mm_Celera | 11:17212840 | CTTTACTCACGGCAA[C/T]CAAGAGAAAACAGCA | 103784 |
rs26851217 | snp | C/T | 0.396694 | 0.202437 | upstream-variant-2KB, intron-variant | Pno1, Wdr92 | Mm_Celera | 11:17212677 | AAAACAGATGCAGGA[C/T]GAGTAGAAACTAACT | 103784 |
rs26851218 | snp | G/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Pno1, Wdr92 | Mm_Celera | 11:17212484 | CTAGTAAATACCACA[G/T]CCTTTCAAGAAGTGT | 103784 |
rs26851219 | snp | A/T | 0.426035 | 0.177515 | upstream-variant-2KB, intron-variant | Pno1, Wdr92 | GRCm38.p3 | 11:17212200 | AGGGTCTGATTCCTC[A/T]ATGCTCCAGCAGAAA | 103784 |
rs26851220 | snp | C/T | 0.297521 | 0.245442 | upstream-variant-2KB | Pno1, Wdr92 | GRCm38.p3 | 11:17211784 | GTAACGGCAGTAAAT[C/T]AGCTTGTGCCATGTG | 103784 |
rs26851221 | snp | C/T | 0.297521 | 0.245442 | upstream-variant-2KB | Pno1, Wdr92 | GRCm38.p3 | 11:17211779 | TTGTGGTAACGGCAG[C/T]AAATTAGCTTGTGCC | 103784 |
rs26851222 | snp | C/G | 0.277778 | 0.248452 | upstream-variant-2KB | Pno1, Wdr92 | GRCm38.p3 | 11:17211677 | CGGAATTGCTGTCCT[C/G]GGATATGCCTGTTTG | 103784 |
rs26851223 | snp | G/T | 0.408163 | 0.193609 | utr-variant-5-prime, upstream-variant-2KB | Pno1, Wdr92 | GRCm38.p3 | 11:17211573 | TTGTACAGCGCATGC[G/T]CCAGCCTCCACCAAT | 103784 |
rs26851224 | snp | A/C | 0.260355 | 0.249785 | utr-variant-5-prime, upstream-variant-2KB | Pno1, Wdr92 | GRCm38.p3 | 11:17211518 | TCCATCTCGGCCAAG[A/C]TCAATCCCGGCAAGT | 103784 |
rs26851225 | snp | C/G | 0.260355 | 0.249785 | synonymous-codon, upstream-variant-2KB | Pno1, Wdr92 | GRCm38.p3 | 11:17211466 | CCCTCTGTGCGTGAC[C/G]GGAGTAAAGCCGTCC | 103784 |
rs26851226 | snp | A/C/G | 0.260355 | 0.249785 | synonymous-codon, upstream-variant-2KB | Pno1, Wdr92 | Mm_Celera | 11:17211373 | CGGCCGCGCCTCCTC[A/C/G]GTGTCCATGCGTCCG | 103784 |
rs26851227 | snp | G/T | 0.497041 | 0.0383476 | intron-variant, upstream-variant-2KB | Pno1, Wdr92 | Mm_Celera | 11:17210935 | ATTGTCTACTTTTAT[G/T]AAGGCTGAAACTACG | 103784 |
rs26851228 | snp | A/G | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Pno1, Wdr92 | Mm_Celera | 11:17210767 | TTGTGATATGGGAAA[A/G]TTAATTTGGCACTGA | 103784 |
rs26851229 | snp | C/T | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Pno1, Wdr92 | GRCm38.p3 | 11:17210448 | ACTAAGAACACAAAC[C/T]AATGACCCTGCAGTA | 103784 |
rs26851230 | snp | C/T | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Pno1, Wdr92 | GRCm38.p3 | 11:17210390 | AAATGATGTGGTATA[C/T]GTTAAGCTATCACTG | 103784 |
rs26851231 | snp | C/G | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Pno1, Wdr92 | GRCm38.p3 | 11:17210337 | CCAGCACTCTCATGT[C/G]TATGGGTGTATATCA | 103784 |
rs26851232 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Pno1, Wdr92 | GRCm38.p3 | 11:17210260 | GCTCTCACCCTATGT[A/G]TGACTCTCGGCAAGT | 103784 |
rs26851233 | snp | C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Pno1, Wdr92 | GRCm38.p3 | 11:17210018 | TTCAGATTTTCACAC[C/T]CAAAACCAGACCCCA | 103784 |
rs26851234 | snp | G/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Pno1, Wdr92 | GRCm38.p3 | 11:17209966 | TCCATTTGAAGAGAT[G/T]ACACATTTGACAAAT | 103784 |
rs28308237 | snp | C/G | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Pno1, Wdr92 | Mm_Celera | 11:17211250 | AACAAAACCGAGAAC[C/G]GACCCTTTCACCTGG | 103784 |
rs29405102 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr92 | Mm_Celera | 11:17219423 | AAGGGCTTGGGGGGG[C/G]GGGATACAATTGTAT | 103784 |
rs29416111 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Pno1, Wdr92 | GRCm38.p3 | 11:17213399 | ATAGATAAGCTTGCA[G/T]GGCAAGGTATGTGGA | 103784 |
rs29424575 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr92 | GRCm38.p3 | 11:17228516 | CTTGCTGATGCCAAG[A/C]ATTTGATGAGGAAAT | 103784 |
rs29434866 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr92 | Mm_Celera | 11:17215370 | TGAATGGAAGGCAGC[A/G]CTTCCTTCCCTAGTT | 103784 |