SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs748855 | snp | A/G | 0.357877 | 0.225527 | intron-variant | NOD2 | GRCh38.p7 | 16:50717487 | ACCTGATGCCTTTAA[A/G]TTGCCCCTCTAGCTG | 64127 |
rs749910 | snp | A/G | 0.17332 | 0.23795 | intron-variant | NOD2 | GRCh38.p7 | 16:50724938 | TCATTCTTAGCCTGT[A/G]ACTTCATTCACATGG | 64127 |
rs751271 | snp | A/C | 0.495596 | 0.0467178 | intron-variant | NOD2 | GRCh38.p7 | 16:50717264 | CGTGGAACTCAGTAA[A/C]CCCAGAAAGCTGTGA | 64127 |
rs1077861 | snp | A/T | 0.44546 | 0.155869 | intron-variant | NOD2 | GRCh38.p7 | 16:50725636 | GCGGCCCAGATCTTA[A/T]TCAGAAATGCCCCTT | 64127 |
rs1078327 | snp | C/T | 0.00258314 | 0.0358454 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711322 | GCGGACCGCCTCATC[C/T]GCCTGCTCCAAGAGA | 64127 |
rs1861756 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | NOD2 | GRCh38.p7 | 16:50724927 | AAGTCACAGGCTAAG[A/G]ATGATGGAACAGGAA | 64127 |
rs1861757 | snp | A/G | 0.319376 | 0.240181 | intron-variant | NOD2 | GRCh38.p7 | 16:50718904 | acttccccttttaGG[A/G]CTTTTCCCCAATAAA | 64127 |
rs1861758 | snp | C/T | 0.365853 | 0.221536 | intron-variant | NOD2 | GRCh38.p7 | 16:50717876 | ctctcctgcacatac[C/T]ggaggactactgTGT | 64127 |
rs1861759 | snp | A/C | 0.442351 | 0.15969 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711672 | CACGACACCTTTGGC[A/C]CGCACCAGGAAGCCA | 64127 |
rs2066842 | snp | C/T | 0.300841 | 0.244784 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710713 | GTGGGCATGGCTGGA[C/T]CCCCGCAGAAGAGCC | 64127 |
rs2066843 | snp | C/T | 0.303319 | 0.244256 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711288 | GTACCTGAGGAAGCG[C/T]CATCATGAGCCCGGG | 64127 |
rs2066844 | snp | C/T | 0.0444529 | 0.142304 | NOD2 | 16 | allele_origin=T(germline)/C(germline) | 16:50712015 | GAGAAGGCCCTGCTC[C/T]GGCGCCAGGCCTGTG | 64127 |
rs2066845 | snp | C/G | 0.0200117 | 0.0980354 | NOD2 | 16 | allele_origin=G(germline)/C(germline) | 16:50722629 | CTTTTCAGATTCTGG[C/G]GCAACAGAGTGGGTG | 64127 |
rs2066846 | in-del | A/CT | 0.375 | 0.216506 | intron-variant | NOD2 | GRCh38.p7 | 16:50725356 | GAATCCCCACAACGT[A/CT]CTTTATCTGTTCTTT | 64127 |
rs2066847 | in-del | -/C | 0.0257735 | 0.110555 | frameshift-variant | NOD2 | GRCh38.p7 | 16:50729867 | AAGCCCTCCTGCAGG[-/C]CCCTTGAAAGGAATG | 64127 |
rs2066850 | snp | A/G | 0.207559 | 0.246371 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696318 | GGGCCCACGTGGGTC[A/G]CCCCTTGACCCTCTC | 64127 |
rs2067085 | snp | C/G | 0.446189 | 0.154969 | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50699948 | GATCTTCACACCGTC[C/G]CAGAGGGTGAGGCAC | 64127 |
rs2076752 | snp | A/G | 0.242201 | 0.249878 | utr-variant-5-prime, intron-variant | NOD2 | GRCh38.p7 | 16:50697185 | CACTGGGCTTTTGGC[A/G]TTCTGCACAAGGCCT | 64127 |
rs2076753 | snp | G/T | 0.317776 | 0.240637 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50699463 | TTCTGGAGAAGTCCC[G/T]CACTGACCTTGTTCT | 64127 |
rs2076754 | snp | C/T | 0.000248602 | 0.0111463 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711206 | CGGCCGCTGTGTCGG[C/T]GTTCCTCAGGAAGTA | 64127 |
rs2076755 | snp | A/T | 0.0950001 | 0.196151 | intron-variant | NOD2 | GRCh38.p7 | 16:50723158 | aaaaaaaaaaaagaa[A/T]aaagaaaGAGCACCG | 64127 |
rs2076756 | snp | A/G | 0.175254 | 0.238565 | intron-variant | NOD2 | GRCh38.p7 | 16:50722970 | cattttatcttaagg[A/G]ccaattccaatccat | 64127 |
rs2111234 | snp | C/T | 0.499663 | 0.0129749 | intron-variant | NOD2 | GRCh38.p7 | 16:50700122 | AAAGAAAGAGTTGTA[C/T]GTTTCCTGCCAAGAG | 64127 |
rs2111235 | snp | C/T | 0.499203 | 0.0199521 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50700058 | TTAGGGGAAATCCCA[C/T]GGACCAAGTTACCCC | 64127 |
rs2357791 | snp | A/G | 0.353371 | 0.227628 | intron-variant | NOD2 | GRCh38.p7 | 16:50730925 | AAAGCTTTGCTGGGC[A/G]TGGCAGCTCACACCT | 64127 |
rs3135499 | snp | A/C | 0.459801 | 0.135955 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732216 | CACAAAAGACCCCTT[A/C]CCACTGCTCTGATGA | 64127 |
rs3135500 | snp | A/G | 0.456332 | 0.141164 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732975 | GGTTAATATTTATAG[A/G]TCACTTTGTTTTACT | 64127 |
rs3813758 | snp | C/T | 3.30153e-05 | 0.00406283 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712189 | GCTCGGAAGGCTGCA[C/T]GTGGCCTGAATGTTG | 64127 |
rs4785224 | snp | A/G | 0.387642 | 0.208697 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696535 | TAGGAAACAGATAAT[A/G]AGTGAATATTTTTTC | 64127 |
rs4785225 | snp | C/G | 0.495174 | 0.0488838 | intron-variant | NOD2 | GRCh38.p7 | 16:50712635 | CTACAACCACCCTGG[C/G]GGGTAGGCAGGAATG | 64127 |
rs4785449 | snp | C/T | 0.496905 | 0.0392151 | intron-variant | NOD2 | GRCh38.p7 | 16:50704636 | cctcctgggtttaag[C/T]gattcttcttcctca | 64127 |
rs4990643 | snp | A/T | 0.35894 | 0.225016 | intron-variant | NOD2 | GRCh38.p7 | 16:50725358 | ATCCCCACAACGTAC[A/T]TTATCTGTTCTTTCT | 64127 |
rs5743259 | snp | G/T | 0.0260105 | 0.111035 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696177 | TCCTGTCTGCAAGGG[G/T]TCAGTGGGCTGAGAT | 64127 |
rs5743260 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696236 | TGGCCCCAGAGAAAC[C/T]GGGCTGGCTGTGGTC | 64127 |
rs5743261 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696659 | GAGAACAGCACTAAG[A/G]CCAGGTTCTCCTCCC | 64127 |
rs5743262 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696881 | GCCCAACGTCACTAG[C/G]TGGGGTGTGTATGGC | 64127 |
rs5743263 | snp | C/T | 0.0325976 | 0.123435 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696954 | GGGGCCCCTACTTAC[C/T]TGTGGCCTGTCCCCT | 64127 |
rs5743264 | snp | C/T | 0.029116 | 0.117091 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697111 | CCTCCGGCTTTTCCT[C/T]TGGGAATTTCCCTTG | 64127 |
rs5743265 | in-del | -/T | 0.0162398 | 0.0886349 | utr-variant-5-prime, intron-variant | NOD2 | GRCh38.p7 | 16:50697148 | GGGTTGGTAGACAGA[-/T]CCAGGCTCACCAGTC | 64127 |
rs5743267 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697469 | CGGCGGGTTTTTTTC[C/T]CCAGGACCTGGGCAG | 64127 |
rs5743268 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | NOD2 | GRCh38.p7 | 16:50707728 | CTCATGTGGTTGTTC[A/G]GTTGTTTTTTTGACC | 64127 |
rs5743269 | snp | C/T | 0.00159675 | 0.0282103 | synonymous-codon, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50707947 | ACCAGTCCCATTGGC[C/T]CTGCCTTTGGAAGGT | 64127 |
rs5743270 | snp | A/G | 0.0520825 | 0.152737 | intron-variant, utr-variant-5-prime | NOD2 | GRCh38.p7 | 16:50708151 | TAAAAGGACAAAAGC[A/G]TGTAATGTTAGCTAT | 64127 |
rs5743271 | snp | A/G | 0.00848912 | 0.0645948 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710777 | CCCCTGGCCACCTCA[A/G]TGACGATGCGGACAC | 64127 |
rs5743272 | snp | A/G | 0.00218928 | 0.0330128 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710966 | CTCTACTCTTTGAGC[A/G]CTGCTGTTGGCCTGA | 64127 |
rs5743273 | snp | C/T | 0.000527478 | 0.0162315 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711105 | CCACTGCTCCCCGAC[C/T]GACCCCACCTCTGTC | 64127 |
rs5743274 | snp | C/T | 0.0058901 | 0.0539477 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711364 | CACGGTTTGTGCCAC[C/T]TGCCTGTCTTCTCAT | 64127 |
rs5743275 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711914 | TGCAGAAGGCCGAGC[C/T]GCACAACCTTCAGAT | 64127 |
rs5743276 | snp | C/G/T | 0.000736013 | 0.0191696 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50711961 | GCAGGGCTGTTGTCC[C/G/T]GGGAGCACTGGGGCC | 64127 |
rs5743277 | snp | C/G/T | 0.00654076 | 0.0568141 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712018 | AAGGCCCTGCTCCGG[C/G/T]GCCAGGCCTGTGCCC | 64127 |
rs5743278 | snp | C/G | 0.00809797 | 0.0631143 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712085 | ACTCCATCCCGCCAG[C/G]TGCACCGGGTGAGGC | 64127 |
rs5743279 | snp | A/G | 0.00590431 | 0.054012 | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712280 | TGCTGCAGCACCTCC[A/G]GCGGCCCGTGGCCCT | 64127 |
rs5743280 | snp | C/T | 0.000181427 | 0.00952263 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712287 | GCACCTCCNGCGGCC[C/T]GTGGCCCTGCAGCTG | 64127 |
rs5743281 | snp | C/T | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50712618 | atgacctcatctaat[C/T]tctacaaccaccctn | 64127 |
rs5743282 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | NOD2 | GRCh38.p7 | 16:50712632 | ntctacaaccaccct[-/G]ggngggtaggcagga | 64127 |
rs5743284 | snp | C/T | 0.00594539 | 0.0541973 | intron-variant | NOD2 | GRCh38.p7 | 16:50716849 | GTGCTCACTGTCCAA[C/T]GTGCTTTGCTTCTGT | 64127 |
rs5743285 | snp | G/T | 0.0024843 | 0.0351565 | intron-variant | NOD2 | GRCh38.p7 | 16:50716880 | GTCTCCTCTCTTCTG[G/T]AACTGAACAGTCTAT | 64127 |
rs5743286 | snp | C/T | 0.00402413 | 0.0446752 | intron-variant | NOD2 | GRCh38.p7 | 16:50720166 | GGCCCTTGACTGCCA[C/T]CTTCATACTTGGTCT | 64127 |
rs5743287 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | NOD2 | GRCh38.p7 | 16:50720242 | CAGTGCCCACGAGCT[C/G]GTGACAGGAAGCCCT | 64127 |
rs5743288 | in-del | -/G | 0.00462326 | 0.0478566 | intron-variant | NOD2 | GRCh38.p7 | 16:50722741 | GCAGTTTTCTTGGGG[-/G]AGATCAGGTGAAGAG | 64127 |
rs5743289 | snp | C/T | 0.0988422 | 0.199274 | NOD2 | 16 | allele_origin=T(germline)/C(germline) | 16:50722863 | TCAAGAGAGGACACT[C/T]GAGTCTTTCTGGGTG | 64127 |
rs5743290 | snp | C/T | 0.0026695 | 0.0364366 | intron-variant | NOD2 | GRCh38.p7 | 16:50723277 | CCCTGCTCTGACATA[C/T]TTTTGTTCCATGATT | 64127 |
rs5743291 | snp | A/G | 0.114777 | 0.210273 | NOD2 | 16 | allele_origin=G(germline)/A(unknown) | 16:50723365 | ATGCTGGCAAAGAAC[A/G]TCATGCTAGAAGAAC | 64127 |
rs5743292 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | NOD2 | GRCh38.p7 | 16:50725820 | CCAATAAAGGGGAGT[A/T]ATCAAGCCAGTTATC | 64127 |
rs5743293 | in-del | -/C | 0.0210502 | 0.100409 | frameshift-variant | NOD2 | GRCh38.p7 | 16:50729870 | CCCTCCTGCAGGCCC[-/C]TTGAAAGGAATGACA | 64127 |
rs5743294 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOD2 | GRCh38.p7 | 16:50729970 | tgtaaaatggggtga[C/T]gggagagaggaatgg | 64127 |
rs5743295 | snp | A/G/T | 0.000181287 | 0.00951929 | missense | NOD2 | GRCh38.p7 | 16:50731752 | TCTGCTTTAGGCTCC[A/G/T]AGGGAACACTTTCTC | 64127 |
rs5743296 | snp | A/C/G | 0.000346661 | 0.0131618 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50731839 | TCCGGGAGGATGTTC[A/C/G]TCTCAGTTTGTTTGT | 64127 |
rs5743297 | snp | C/T | 0.0240643 | 0.107019 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732340 | CCTCCTGGACTCCTG[C/T]ACACGCTCCTTCCTC | 64127 |
rs5743298 | snp | G/T | 0.0215028 | 0.101435 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732559 | TATGACCACACTCCA[G/T]CTGGGATCACATGTG | 64127 |
rs5743299 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50732842 | GAAAAAAAATTAGGC[C/T]GTTCCTTCAAAGCAA | 64127 |
rs5743300 | snp | A/C | 0.0599851 | 0.162463 | downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50733208 | ttgagaccaacctga[A/C]caacatggagaaacc | 64127 |
rs5816717 | snp | A/C | | | intron-variant | NOD2 | GRCh38.p7 | 16:50725357 | AATCCCCACAACGTA[A/C]TTTATCTGTTCTTTC | 64127 |
rs6413461 | snp | C/T | 1.65833e-05 | 0.00287948 | synonymous-codon, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50712107 | GGGTGAGGCCAAGAG[C/T]GTGCATGCCATGCCC | 64127 |
rs6500328 | snp | A/G | 0.440471 | 0.161928 | intron-variant | NOD2 | GRCh38.p7 | 16:50702745 | AAGCCTCACAAGGGT[A/G]TAGTGTGACTACACT | 64127 |
rs7187857 | snp | A/G | 0.494315 | 0.0530107 | intron-variant | NOD2 | GRCh38.p7 | 16:50726927 | gggtggatcacctga[A/G]gtggggagttccata | 64127 |
rs7190413 | snp | A/T | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50701628 | CAAGATTGTGTCTTG[A/T]CATCTTTAAAAGTTC | 64127 |
rs7198979 | snp | A/G | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50718369 | gcgtatagagcgtgg[A/G]tgcgctggacggggg | 64127 |
rs7203344 | snp | A/G | 0.206336 | 0.246157 | intron-variant | NOD2 | GRCh38.p7 | 16:50731465 | TTGACAGATTCTCTT[A/G]TTGCCTTAAAAAGAA | 64127 |
rs7203691 | snp | A/G | 0.368733 | 0.220005 | intron-variant | NOD2 | GRCh38.p7 | 16:50719513 | GCCCAGCGCTCTTGT[A/G]CAACAGGTAAAGCCT | 64127 |
rs7204911 | snp | C/T | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50704427 | actggattgatagtt[C/T]ggctgggtataaaat | 64127 |
rs7206340 | snp | C/T | 0.0260105 | 0.111035 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50698511 | TATTCTGAGTCTACC[C/T]CTTGGAGTAGCAGTG | 64127 |
rs7206582 | snp | A/G | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50701805 | tcatgatggaaatca[A/G]aaaatattcagaacc | 64127 |
rs7359452 | snp | A/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50731080 | gaggctgggatggaa[A/G]gatcccttgaaccca | 64127 |
rs7498256 | snp | C/G | | | missense, nc-transcript-variant | NOD2 | GRCh38.p7 | 16:50710916 | ATTCAGCTGCCGGCA[C/G]CTGCAGTGCATGGCC | 64127 |
rs7500036 | snp | C/T | 0.216048 | 0.247684 | intron-variant | NOD2 | GRCh38.p7 | 16:50703587 | gatgttgcagtgagc[C/T]gagatcgcactgctt | 64127 |
rs7500826 | snp | A/G | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50704520 | caatattgcttctaa[A/G]aattccaaaaccttt | 64127 |
rs8045009 | snp | C/T | 0.365646 | 0.221644 | intron-variant | NOD2 | GRCh38.p7 | 16:50702030 | AAATCACTGAAGTCT[C/T]GAACTTCTGGGCTGA | 64127 |
rs8046608 | snp | C/T | 0.0433465 | 0.140692 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50696970 | TGTGGCCTGTCCCCT[C/T]GTGAATGTGTCTCAT | 64127 |
rs8057341 | snp | A/G | 0.49934 | 0.0181589 | intron-variant | NOD2 | GRCh38.p7 | 16:50704069 | GGCAGCGGGAGTTGA[A/G]AAGAAACGATATTAG | 64127 |
rs8061316 | snp | A/G | 0.0260105 | 0.111035 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697807 | CTGTGCCCCAGCAGC[A/G]TTCTGAGAGATTGGA | 64127 |
rs8061636 | snp | C/G | 0.0260105 | 0.111035 | upstream-variant-2KB, intron-variant | NOD2 | GRCh38.p7 | 16:50697984 | GACGAGTAAGACCCA[C/G]GCTCCCACGTGGCCC | 64127 |
rs8061960 | snp | C/T | 0.36021 | 0.224397 | intron-variant | NOD2 | GRCh38.p7 | 16:50727523 | taaaaattcatgctt[C/T]gggattcaacaaact | 64127 |
rs8063130 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NOD2 | GRCh38.p7 | 16:50722918 | CAGGGTTTTGATACA[C/G]TATCTGTAAATTGAA | 64127 |
rs9921146 | snp | A/C | 0.494526 | 0.0520291 | intron-variant | NOD2 | GRCh38.p7 | 16:50726069 | TCAGGCAGAGAGTGG[A/C]AGGTCTTCTCTGCAA | 64127 |
rs9925315 | snp | A/T | 0.495445 | 0.0475058 | intron-variant, utr-variant-3-prime | NOD2 | GRCh38.p7 | 16:50715463 | ttctgttgcccaggc[A/T]gggggtacagtggca | 64127 |
rs9931711 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, downstream-variant-500B | NOD2 | GRCh38.p7 | 16:50713759 | GGGAAGGTATGGAGA[C/T]GGCTGCCTGAGCTTC | 64127 |
rs10451131 | snp | C/G | | | intron-variant | NOD2 | GRCh38.p7 | 16:50710180 | ATCCCAGCCCAGAGC[C/G]CCTTCCCGTCATCTA | 64127 |
rs10521209 | snp | G/T | 0.362523 | 0.223246 | intron-variant | NOD2 | GRCh38.p7 | 16:50721798 | TTGCTCAGCCTGACC[G/T]CATTTTTCAAAGAGC | 64127 |
rs11292073 | in-del | -/A | 0 | 0 | intron-variant | NOD2 | GRCh38.p7 | 16:50723101 | AAAAAAAAAAAAAAA[-/A]GAGCACTGCATTCAA | 64127 |