SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1908 | snp | C/T | 0.140242 | 0.224618 | utr-variant-3-prime, nc-transcript-variant | NEDD9 | GRCh38.p7 | 6:11184928 | GACAAGTTTTCTGTA[C/T]AGTTTATGTCTCAGA | 4739 |
rs1911 | snp | A/G | 0.357877 | 0.225527 | utr-variant-3-prime, nc-transcript-variant | NEDD9 | GRCh38.p7 | 6:11184951 | GTCTCAGATACTTCT[A/G]TGTATACATAAGAAC | 4739 |
rs2034 | snp | A/C | 0.390277 | 0.206936 | intron-variant, utr-variant-3-prime | NEDD9 | GRCh38.p7 | 6:11200623 | AATGAAGATTTAATC[A/C]TTCCTAAATTTAAGT | 4739 |
rs2950 | snp | A/G | 0.309401 | 0.24284 | intron-variant, upstream-variant-2KB | NEDD9, LOC107986565 | GRCh38.p7 | 6:11350032 | CTGTGAACTATGAAC[A/G]TCTCAGCCTAGAAGG | 4739 |
rs3102 | snp | C/T | 0.264084 | 0.249603 | intron-variant | NEDD9 | GRCh38.p7 | 6:11208647 | CAGCCATGGCCCCTG[C/T]GCTGATGGAGCTTGT | 4739 |
rs10601 | snp | A/T | 0.186737 | 0.241863 | utr-variant-3-prime, nc-transcript-variant | NEDD9 | GRCh38.p7 | 6:11185024 | CATTTTATGGGTCAG[A/T]CAACTTTCAGAAATT | 4739 |
rs13849 | snp | A/C | 0.189261 | 0.242509 | utr-variant-3-prime, nc-transcript-variant | NEDD9 | GRCh38.p7 | 6:11183663 | AATGCATGATCTCAG[A/C]GTGATTAAAAAAAAA | 4739 |
rs361521 | snp | A/G | 0.393803 | 0.204501 | intron-variant | NEDD9 | GRCh38.p7 | 6:11208582 | GTTCACTGGGCTGCT[A/G]TCTGTGGGCTGATGC | 4739 |
rs726230 | snp | G/T | 0.232481 | 0.249385 | intron-variant, downstream-variant-500B, nc-transcript-variant | NEDD9 | GRCh38.p7 | 6:11200341 | CTTCTGCCAGCCTCA[G/T]AGGCAAGCATACATC | 4739 |
rs729747 | snp | A/G | 0.132409 | 0.220618 | intron-variant | NEDD9 | GRCh38.p7 | 6:11217643 | ACAAAAGAAAAAAAT[A/G]AGCCTCAAGAAGTTA | 4739 |
rs738271 | snp | A/T | 0.42574 | 0.177808 | intron-variant | NEDD9 | GRCh38.p7 | 6:11367054 | GAGGTAACCCTCCTT[A/T]CTTAATGTTCAGTAC | 4739 |
rs742115 | snp | C/T | 0.447032 | 0.153878 | intron-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11326788 | TACCATCTTCCTTCC[C/T]CCTCCACTCAGGAAC | 4739 |
rs744970 | snp | A/G | 0.371987 | 0.218218 | intron-variant | NEDD9 | GRCh38.p7 | 6:11243624 | CCTGTTATGAAATCA[A/G]CTCCTTCGGTTTCCA | 4739 |
rs760678 | snp | C/G | 0.375996 | 0.215928 | intron-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11334421 | GGGCACCCTTATCTT[C/G]CCCGATTTGTACAAA | 4739 |
rs760679 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11292331 | GCTGACCAAGGTCCA[A/G]AAAATAAACAGGAGC | 4739 |
rs760680 | snp | C/T | 0.44651 | 0.154543 | intron-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11292056 | AAGTAAGTCTATTTT[C/T]CCCAAATGATCAATA | 4739 |
rs767231 | snp | A/G | 0.494855 | 0.0504572 | intron-variant | NEDD9 | GRCh38.p7 | 6:11242903 | ATGGCTGTGTCCCAT[A/G]AGCAAAGGCATGCAT | 4739 |
rs767232 | snp | A/G | 0.492966 | 0.0588865 | intron-variant | NEDD9 | GRCh38.p7 | 6:11243060 | TTACTGTGGATGAGC[A/G]AATATGAGCCACAAA | 4739 |
rs909637 | snp | A/G | 0.466308 | 0.125343 | intron-variant | NEDD9 | GRCh38.p7 | 6:11357920 | GGCGGGACCCACAGG[A/G]ACTGCCTGGGTGGAA | 4739 |
rs926314 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | NEDD9 | GRCh38.p7 | 6:11360617 | AGAAAGCTCATCTTC[C/T]ATGACTGGAGCAGGA | 4739 |
rs932309 | snp | C/T | 0.469544 | 0.119585 | intron-variant | NEDD9 | GRCh38.p7 | 6:11277527 | TCTGTCTCTTTTCCA[C/T]CCCCTGCCCATGCCT | 4739 |
rs941982 | snp | A/G | 0.184584 | 0.24129 | synonymous-codon, nc-transcript-variant | NEDD9 | GRCh38.p7 | 6:11190393 | CTGGTGGGAGTCTTC[A/G]ACTCGTTGCAGCTCC | 4739 |
rs943007 | snp | C/G | 0.130008 | 0.219321 | intron-variant | NEDD9 | GRCh38.p7 | 6:11217495 | GTAACTCTATATTCA[C/G]TTGGATGGTTAGTCT | 4739 |
rs943008 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | NEDD9 | GRCh38.p7 | 6:11219939 | GAAGATCTGGAATGT[C/T]GAATTTTTTGAGTTG | 4739 |
rs943009 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | NEDD9 | GRCh38.p7 | 6:11243658 | CAGTGGGCTCTTCTG[A/G]TTCTTCTACTTCTCT | 4739 |
rs960944 | snp | G/T | 0.158302 | 0.232576 | intron-variant | NEDD9 | GRCh38.p7 | 6:11187764 | AAACCAGAAAATAGG[G/T]GAGAGTGAAGTAGAC | 4739 |
rs960945 | snp | C/T | 0.227664 | 0.249 | intron-variant | NEDD9 | GRCh38.p7 | 6:11187779 | TGAGAGTGAAGTAGA[C/T]TGATAGAAAGAAGCA | 4739 |
rs967473 | snp | C/T | 0.219947 | 0.248187 | intron-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11329190 | CATAAAGATGTTTGC[C/T]CTTGCACGGGTGTTT | 4739 |
rs1009666 | snp | A/G | 0.18134 | 0.240387 | intron-variant | NEDD9 | GRCh38.p7 | 6:11216840 | AGATAGGTACAAAAC[A/G]TATATAATAGCATCA | 4739 |
rs1009667 | snp | A/G | 0.487746 | 0.0773096 | intron-variant | NEDD9 | GRCh38.p7 | 6:11214472 | TCGCCCTCCCCTTTC[A/G]TCACCTACTTCTTGA | 4739 |
rs1012502 | snp | C/T | 0.442926 | 0.158996 | intron-variant | NEDD9 | GRCh38.p7 | 6:11365258 | TAGGTCTATGGAATG[C/T]TGGGGTCACTTGGTT | 4739 |
rs1012503 | snp | C/T | 0.394354 | 0.204112 | intron-variant | NEDD9 | GRCh38.p7 | 6:11364886 | GGCTTATAAAGGAAC[C/T]GTACCATAATAGTTA | 4739 |
rs1013678 | snp | C/T | 0.449034 | 0.157721 | intron-variant | NEDD9 | GRCh38.p7 | 6:11363972 | caagcaggattgaga[C/T]agcagtctcagacct | 4739 |
rs1018374 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | NEDD9 | GRCh38.p7 | 6:11277673 | CTGAGATGGTTCAAC[A/G]CTGCTATGGGCAAAA | 4739 |
rs1044408 | snp | A/G | 0.473451 | 0.112115 | utr-variant-3-prime, nc-transcript-variant | NEDD9 | GRCh38.p7 | 6:11183679 | GGATTTAAAAAACAA[A/G]AATGCATGATCTCAG | 4739 |
rs1044411 | snp | A/T | 0.473451 | 0.112115 | utr-variant-3-prime, nc-transcript-variant | NEDD9 | GRCh38.p7 | 6:11183670 | AAACAAGAATGCATG[A/T]TCTCAGAGTGATTAA | 4739 |
rs1044417 | snp | A/G | 0.499824 | 0.00938333 | utr-variant-3-prime, nc-transcript-variant | NEDD9 | GRCh38.p7 | 6:11183354 | GTATTACTCTTTGCC[A/G]TCTTGTATGTAGAGG | 4739 |
rs1050775 | snp | C/T | 0.499821 | 0.00944844 | synonymous-codon, nc-transcript-variant | NEDD9 | GRCh38.p7 | 6:11185300 | CGAGCAGCTCAAGAC[C/T]ATAGTCATGGCAACC | 4739 |
rs1076051 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | NEDD9 | GRCh38.p7 | 6:11244445 | AGGTGGGAGAAAGAA[A/G]TAAAAGATCAGTCTG | 4739 |
rs1465131 | snp | C/T | 0.200815 | 0.245114 | intron-variant | NEDD9 | GRCh38.p7 | 6:11192342 | TTGTAGTCACTCACT[C/T]ACCCCTTTTGTAGGC | 4739 |
rs1475344 | snp | C/T | 0.479663 | 0.0987666 | intron-variant | NEDD9 | GRCh38.p7 | 6:11228760 | TGTGTAGGTAAGCCA[C/T]TTAGCTCTGCAAATG | 4739 |
rs1475345 | snp | A/G | 0.442926 | 0.158996 | intron-variant | NEDD9 | GRCh38.p7 | 6:11230169 | ACTTCATTTTGCTTT[A/G]TAGAGTTACTATCTT | 4739 |
rs1475346 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NEDD9 | GRCh38.p7 | 6:11230243 | TAAACTTTCTGGGAG[A/G]AGAAAACACTGGCCA | 4739 |
rs1569465 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NEDD9 | GRCh38.p7 | 6:11364444 | CCTTTGGGgggaatt[C/T]ccaaggccaccccca | 4739 |
rs1569466 | snp | G/T | 0.484561 | 0.0864924 | intron-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11309533 | caaagcaggcaaggt[G/T]ctgtgagcctgtagt | 4739 |
rs1570372 | snp | A/G | 0.499824 | 0.00938333 | utr-variant-3-prime, nc-transcript-variant | NEDD9 | GRCh38.p7 | 6:11183857 | CTCTTGGTAATATGT[A/G]AATACATTTACCCAT | 4739 |
rs1570373 | snp | A/G | 0.485731 | 0.0832509 | intron-variant | NEDD9 | GRCh38.p7 | 6:11202326 | TGCCTGTTGGAAAGG[A/G]CTTCTTTCACTTAAA | 4739 |
rs1570374 | snp | G/T | 0.429987 | 0.173507 | intron-variant | NEDD9 | GRCh38.p7 | 6:11203673 | CCAGGATGAAGTGCT[G/T]TCTTAGCTCTTGGTA | 4739 |
rs1803710 | snp | G/T | 0.210301 | 0.246828 | utr-variant-3-prime, nc-transcript-variant | NEDD9 | GRCh38.p7 | 6:11184634 | GACTTATTCTTGTTT[G/T]GAAAACTCTTTTCAA | 4739 |
rs1803711 | snp | C/T | | | missense, nc-transcript-variant | NEDD9 | GRCh38.p7 | 6:11185407 | GTCATCCTCAGTGCA[C/T]ACAAACTGGTGTTCA | 4739 |
rs1810451 | snp | C/T | 0.43655 | 0.16643 | intron-variant | NEDD9 | GRCh38.p7 | 6:11358120 | CTGGGACTACAGGCA[C/T]GCAGCACGCACGCCC | 4739 |
rs1883235 | snp | G/T | 0.403334 | 0.197456 | intron-variant | NEDD9 | GRCh38.p7 | 6:11357216 | TCCACAGGAGTAAAG[G/T]GTTAGAGCAGCCAGA | 4739 |
rs1883236 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11333163 | TGCTGATAGACAAAG[C/T]CTCGGAAAAAAATGC | 4739 |
rs1883237 | snp | C/T | 0.352721 | 0.227922 | intron-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11332893 | TATGCAGCATTTATT[C/T]TGCTGAAGAGAAAAC | 4739 |
rs1883238 | snp | C/T | 0.377582 | 0.214995 | intron-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11329582 | CAGGCACATTGTAAG[C/T]GCTCTTAAAACATTA | 4739 |
rs1883239 | snp | A/G | 0.278133 | 0.248412 | intron-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11329367 | TTCCAGCCAAGGTGA[A/G]GGAGTTGCCCCGGGC | 4739 |
rs1883240 | snp | C/T | 0.4661 | 0.125701 | intron-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11319132 | GGAATCTTTTCAAGC[C/T]GAGCAGATATTCCAC | 4739 |
rs1883241 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | NEDD9 | GRCh38.p7 | 6:11285340 | TTTATTTATATCTTC[C/T]TTAATTTTTCTCAAC | 4739 |
rs1885662 | snp | A/G | 0.152667 | 0.230274 | intron-variant | NEDD9 | GRCh38.p7 | 6:11191420 | TGCAGACTCGTATGT[A/G]CAACCCTCCTGGCTA | 4739 |
rs1967812 | snp | A/C | 0.199114 | 0.249412 | intron-variant | NEDD9 | GRCh38.p7 | 6:11228423 | TAATCCCAGCTACTC[A/C]GGAGGCCGAGACAGG | 4739 |
rs1997662 | snp | C/T | 0.440884 | 0.161442 | intron-variant | NEDD9 | GRCh38.p7 | 6:11249935 | GCAGGAATCTCTGGG[C/T]CCCTTGACCATGATC | 4739 |
rs2003663 | snp | A/C | 0.0558544 | 0.157504 | intron-variant, nc-transcript-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11334757 | ctttttgtttaacat[A/C]atttccatagtctaa | 4739 |
rs2003664 | snp | A/T | 0.34659 | 0.230587 | intron-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11334667 | ATGCCCATTAAAATG[A/T]TGTATAACATAACCA | 4739 |
rs2018334 | snp | A/G | 0.494651 | 0.0514399 | intron-variant | NEDD9 | GRCh38.p7 | 6:11217610 | CTTTAAACAATTACC[A/G]TCCAACCCTTTCACT | 4739 |
rs2018336 | snp | C/T | 0.227959 | 0.249026 | intron-variant | NEDD9 | GRCh38.p7 | 6:11217664 | CAAGAAGTTAATGAT[C/T]TGCCAGCTCACCTGG | 4739 |
rs2025676 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | NEDD9 | GRCh38.p7 | 6:11240567 | TATGGCTAATATCTT[A/G]ACTTGATGTTTAAAA | 4739 |
rs2025677 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | NEDD9 | GRCh38.p7 | 6:11223878 | GCACAACATCTTAGA[C/T]AGTTTCCTGCAAAAG | 4739 |
rs2025678 | snp | A/T | 0.093777 | 0.195178 | intron-variant | NEDD9 | GRCh38.p7 | 6:11224780 | GTGTTGGGGGGCAGA[A/T]AAGCCCAGCTCATTC | 4739 |
rs2049959 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | NEDD9 | GRCh38.p7 | 6:11289507 | caagatcgcgccact[A/G]cattccagcctgggc | 4739 |
rs2049960 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | NEDD9 | GRCh38.p7 | 6:11289256 | ATATAAAAGAGTACA[A/G]TGGAAGAATTCAATC | 4739 |
rs2049961 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | NEDD9 | GRCh38.p7 | 6:11289093 | CAATAAGATGAATGC[A/G]TTTGCTGAGCATAGG | 4739 |
rs2064111 | snp | A/G | 0.493969 | 0.05458 | intron-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11316205 | AACTCAAAGGTCTGC[A/G]TAGAGATGAATCAGA | 4739 |
rs2064112 | snp | A/G | 0.412082 | 0.190341 | intron-variant | NEDD9 | GRCh38.p7 | 6:11339536 | AGTTGCACAACAGAC[A/G]TAAGCTGCTCCACTT | 4739 |
rs2066919 | snp | A/G | 0.246485 | 0.249975 | intron-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11321386 | TTTCTGTGATGTAAC[A/G]CACACAGGTTTTCAC | 4739 |
rs2072834 | snp | C/T | 0.39527 | 0.203462 | intron-variant, upstream-variant-2KB | NEDD9, LOC105374925 | GRCh38.p7 | 6:11297428 | AGCCTGTGCTAAACT[C/T]ATAAATACTCTTAAA | 4739 |
rs2078599 | snp | A/G | 0.118235 | 0.212457 | intron-variant, downstream-variant-500B | NEDD9 | GRCh38.p7 | 6:11200188 | TGGTTTGGGGTCCCT[A/G]CCTTGGTGAGCCCTA | 4739 |
rs2092142 | snp | C/T | 0.45762 | 0.139261 | intron-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11302207 | tctgatggtagtttg[C/T]atttctgtgggatca | 4739 |
rs2094175 | snp | C/G | 0.18369 | 0.241386 | intron-variant | NEDD9 | GRCh38.p7 | 6:11225722 | TAGCCATGATGGTCT[C/G]GATCTCCTGACCTCG | 4739 |
rs2142739 | snp | C/T | 0.15698 | 0.23205 | intron-variant | NEDD9 | GRCh38.p7 | 6:11273344 | GTCTTAAGTAACTGA[C/T]ACCTCTGTGCTAGTT | 4739 |
rs2142740 | snp | A/G | 0.15698 | 0.23205 | intron-variant | NEDD9 | GRCh38.p7 | 6:11273286 | CACATTTTCAAGAAT[A/G]TATCTATTAGGTAAA | 4739 |
rs2142741 | snp | C/T | 0.402806 | 0.197864 | intron-variant | NEDD9 | GRCh38.p7 | 6:11262090 | GGCACATGTTTGGCA[C/T]CAATTTTCTACACTG | 4739 |
rs2142742 | snp | A/G | 0.198014 | 0.244535 | intron-variant, upstream-variant-2KB | NEDD9, LOC105374925 | GRCh38.p7 | 6:11295891 | CATCACACACCTAAC[A/G]TGGGTGTAATGTGTC | 4739 |
rs2146341 | snp | A/T | 0.18325 | 0.240924 | intron-variant | NEDD9 | GRCh38.p7 | 6:11196584 | AGGATGCCTGTGGTC[A/T]TCTGGTTTTTTAAAA | 4739 |
rs2146342 | snp | C/T | 0.394904 | 0.203722 | intron-variant | NEDD9 | GRCh38.p7 | 6:11202124 | CATTCATAGTACCTA[C/T]GATTCTCTGAATTTA | 4739 |
rs2179178 | snp | A/G | 0.48498 | 0.0853497 | intron-variant | NEDD9 | GRCh38.p7 | 6:11363108 | AAGTCTATGCATTGA[A/G]ATGAAGTCATTGACT | 4739 |
rs2179179 | snp | A/G | 0.428937 | 0.17459 | intron-variant | NEDD9 | GRCh38.p7 | 6:11346339 | CAGTTAAGGGCTGCC[A/G]CCATCATGACATGGA | 4739 |
rs2182335 | snp | G/T | 0.427727 | 0.175821 | intron-variant | NEDD9 | GRCh38.p7 | 6:11216744 | ATGTTTTATTTAATT[G/T]GCTAGATGGCCCTTG | 4739 |
rs2182336 | snp | C/T | 0.249038 | 0.249998 | intron-variant | NEDD9 | GRCh38.p7 | 6:11227152 | TATTAGCAAGTGGGG[C/T]CATATGCTGTTAGGG | 4739 |
rs2182337 | snp | C/T | 0.231189 | 0.249291 | intron-variant | NEDD9 | GRCh38.p7 | 6:11235449 | gaggggaggatacag[C/T]agtagcccagacaaa | 4739 |
rs2208840 | snp | A/G | 0.188946 | 0.24243 | downstream-variant-500B | NEDD9 | GRCh38.p7 | 6:11183151 | TGACACATATACAGA[A/G]AAAACCAAACCCTCA | 4739 |
rs2223292 | snp | C/T | 0.350546 | 0.22889 | intron-variant | NEDD9, LOC105374925 | GRCh38.p7 | 6:11332652 | AGTTGGGAGGTCACT[C/T]AAATAGAACACGACG | 4739 |
rs2236348 | snp | C/T | 0.465263 | 0.127129 | intron-variant | NEDD9 | GRCh38.p7 | 6:11187920 | CTTGCTTAGGCTAGC[C/T]TGAATGGGTCTTGTT | 4739 |
rs2281063 | snp | A/G | 0.457271 | 0.139781 | intron-variant, upstream-variant-2KB | NEDD9, LOC105374925 | GRCh38.p7 | 6:11298030 | GTAACAGCTATTCAG[A/G]AGGCTGAGGCATGAG | 4739 |
rs2281064 | snp | A/T | 0.493293 | 0.0575177 | intron-variant, upstream-variant-2KB | NEDD9, LOC105374925 | GRCh38.p7 | 6:11297784 | TTTCTTCATCTACAA[A/T]ATGAGAATGAGAATA | 4739 |
rs2281874 | snp | A/C | 0.459233 | 0.136827 | intron-variant | NEDD9 | GRCh38.p7 | 6:11223849 | TTGTTATTTACAAGT[A/C]AATGAAAAAAAAAGC | 4739 |
rs2281875 | snp | A/G | 0.084364 | 0.187256 | intron-variant | NEDD9 | GRCh38.p7 | 6:11223909 | GCTGCTGTAAGGGAG[A/G]TGGGATAATGCCTTC | 4739 |
rs2281876 | snp | C/T | 0.084728 | 0.187577 | intron-variant | NEDD9 | GRCh38.p7 | 6:11224354 | GAGAAAGGAGGCTGT[C/T]GGGCTGCGTTCATTT | 4739 |
rs2296567 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | NEDD9 | GRCh38.p7 | 6:11232451 | TACACAAGCACACAC[C/T]CGCAGGCACAGCTTT | 4739 |
rs2327332 | snp | C/T | 0.260227 | 0.249791 | intron-variant | NEDD9 | GRCh38.p7 | 6:11217891 | CAAGCTTCCTTGAAA[C/T]TGTCTTCTTCTGGCC | 4739 |
rs2327389 | snp | C/T | 0.144969 | 0.226867 | intron-variant | NEDD9 | GRCh38.p7 | 6:11241725 | GCATTTTCTCCCCCT[C/T]GTGCCTTAAAAGAGC | 4739 |