Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,096,234 C→G P131R (CCG→CGG)  ycdU → uncharacterized protein YcdU

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,096,2340CG100.0% 54.9 / NA 17P131R (CCG→CGG) ycdUuncharacterized protein YcdU
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base G (6/11);  total (6/11)

TGAGTGCAATGAGTTGGGGGCTATACCAGCTTCTACCCTCGTTATATGCGCTGTTCCTGATTTCGTTACTTGGGCCGTTGGTCATCTTTCTGCTGTTTCGGATGATCCGCACCAGTTATGTCAAGCAGGTCGCTATTTCAGTAGCGAAAA  >  NC_000913/1096159‑1096308
                                                                           |                                                                          
tGAGTGCAATGAGTTGGGGGCTATACCAGCTTCTACCCTCGTTATATGCGCTGTTCCTGATTTCGTTACTTGGGCGGTTgg                                                                       >  2:200549/1‑81 (MQ=255)
  aGTGCAATGAGTTGGGGGCTATACCAGCTTCTACCCTCGTTATATGCGCTGTTCCTGATTTCGTTACTTGGGCGGTTGGt                                                                      <  1:200527/80‑1 (MQ=255)
    tGCAATGAGTTGGGGGCTATACCAGCTTCTACCCTCGTTATATGCGCTGTTCCTGATTTCGTTACTTGGGCGGTTGGTCAt                                                                   <  1:200528/81‑1 (MQ=255)
                ggggCTATACCAGCTTCTACCCTCGTTATATGCGCTGTTCCTGATTTCGTTACTTGGGCGGTTGGTCATCTTTCTGCTGtt                                                       <  2:200529/81‑1 (MQ=255)
                   gCTATACCAGCTTCTACCCTCGTTATATGCGCTGTTCCTGATTTCGTTACTTGGGCGGTTGGTCATCTTTCTGCTGTTTCg                                                    <  1:200530/81‑1 (MQ=255)
                              ttCTACCCTCGTTATATGCGCTGTTCCTGATTTCGTTACTTGGGCGGTTGGTCATCTTTCTGCTGTTTCGGATGATCCGCa                                         >  1:200553/1‑81 (MQ=255)
                                cTACCCTCGTTATATGCGCTGTTCCTGATTTCGTTACTTGGGCGGTTGGTCATCTTTCTGCTGTTTCGGATGATCCGCAc                                        >  1:200558/1‑80 (MQ=255)
                                        gTTATATGCGCTGTTCCTGATTTCGTTACTTGGGCGGTTGGTCATCTTTCTGCTGTTTCGGATGATCCGCACCAGTTAt                                 <  1:200531/79‑1 (MQ=255)
                                         ttATATGCGCTGTTCCTGATTTCGTTACTTGGGCGGTTGGTCATCTTTCTGCTGTTTCGGATGATCCGCACCAGTTATGTc                              <  2:200532/81‑1 (MQ=255)
                                                  cTGTTCCTGATTTCGTTACTTGGGCGGTTGGTCATCTTTCTGCTGTTTCGGATGATCCGCACCAGTTATGTCAAGCAGGTc                     <  1:200533/81‑1 (MQ=255)
                                                   tGTTCCTGATTTCGTTACTTGGGCGGTTGGTCATCTTTCTGCTGTTTCGGATGATCCGCACCAGTTATGTCAAGCAGTTCg                    >  2:200561/1‑81 (MQ=255)
                                                        cTGATTTCGTTACTTGGGCGGTTGGTCATCTTTCTGCTGTTTCGGATGATCCGCACCAGTTATGTCAAGCAGGTCGCTAtt               <  2:200534/81‑1 (MQ=255)
                                                            tttCGTTGCTTGGGCGGTTGGTCATCTTTCTGCTGTTTCGGATGATCCGCACCAGTTATGTCAAGCAGGTCGCTATTTCAg           <  2:200535/81‑1 (MQ=255)
                                                                   aCTTGGGCGGTTGGTCATCTTTCTGCTGTTTCGGATGATCCGCACCAGTTATGTCAAGCAGGTCGCTATTTCAGTAGCGa     >  1:200563/1‑80 (MQ=255)
                                                                    cTTGGGCGGTTGGTCATCTTTCTGCTGTTTCGGATGATCCGCACCAGTTATGTCAAGCAGGTCGCTATTTCAGTAGCGaaa   <  2:200537/81‑1 (MQ=255)
                                                                    cTTGGGCGGTTGGTCATCTTTCTGCTGTTTCGGATGATCCGCACCAGTTATGTCAAGCAGGTCGCTATTTCAGTAGCGaa    <  1:200536/80‑1 (MQ=255)
                                                                       gggCGGTTGGTCATCTTTCTGCTGTTTCGGATGATCCGCACCAGTTATGTCAAGCAGGTCGCTATTTCAGTAGCGaaag  >  2:200560/1‑78 (MQ=255)
                                                                           |                                                                          
TGAGTGCAATGAGTTGGGGGCTATACCAGCTTCTACCCTCGTTATATGCGCTGTTCCTGATTTCGTTACTTGGGCCGTTGGTCATCTTTCTGCTGTTTCGGATGATCCGCACCAGTTATGTCAAGCAGGTCGCTATTTCAGTAGCGAAAA  >  NC_000913/1096159‑1096308

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: