Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,931,057 T→C I59I (ATT→ATC purT → phosphoribosylglycinamide formyltransferase 2

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,931,0570TC100.0% 81.3 / NA 24I59I (ATT→ATCpurTphosphoribosylglycinamide formyltransferase 2
Reads supporting (aligned to +/- strand):  ref base T (0/0);  new base C (9/15);  total (9/15)

GGCGTAGAGGTGATTGCCGTCGATCGCTATGCCGACGCACCAGCCATGCATGTCGCGCATCGCTCCCATGTCATTAATATGCTTGATGGTGATGCATTACGCCGTGTGGTTGAACTGGAAAAACCACATTATATCGTGCCGGAGATCGAA  >  NC_000913/1930983‑1931132
                                                                          |                                                                           
ggCGTAGAGGTGATTGCCGTCGATCGCTATGCCGACGCACCAGCCATGCATGTCGCGCATCGCTCCCATGTCATCAat                                                                          <  2:306795/78‑1 (MQ=255)
 gCGTAGAGGTGATTGCCGTCGATCGCTATGCCGACGCACCAGCCATGCATGTCGCGCATCGCTCCCATGTCATCAATATGc                                                                      <  1:306796/81‑1 (MQ=255)
     agagGTGATTGCCGTCGATCGCTATGCCGACGCACCAGCCATGCATGTCGCGCATCGCTCCCATGTCATCAATATGCTTGa                                                                  >  2:306833/1‑81 (MQ=255)
        ggTGATTGCCGTCGATCGCTATGCCGACGCACCAGCCATGCATGTCGCGCATCGCTCCCATGTCATCAATATGCTTGATgg                                                               >  2:306843/1‑81 (MQ=255)
               gCCGTCGATCGCTATGCCGACGCACCAGCCATGCATGTCGCGCATCGCTCCCATGTCATCAATATGCTTGATGGTGATGc                                                         <  2:306797/80‑1 (MQ=255)
                ccGTCGATCGCTATGCCGACGCACCAGCCATGCATGTCGCGCATCGCTCCCATGTCATCAATATGCTTGATGGTGATGCAt                                                       <  1:306798/81‑1 (MQ=255)
                  gTCGATCGCTATGCCGACGCACCAGCCATGCATGTCGCGCATCGCTCCCATGTCATCAATATGCTTGATGGTGATGCATTa                                                     >  1:306834/1‑81 (MQ=255)
                   tCGATCGCTATGCCGACGCACCAGCCATGCATGTCGCGCATCGCTCCCATGTCATCAATATGCTTGATGGTGATGCATTAc                                                    <  1:306799/81‑1 (MQ=255)
                      aTCGCTATGCCGACGCACCAGCCATGCATGTCGCGCATCGCTCCCATGTCATCAATATGCTTGATGGTGATGCATTACGcc                                                 >  2:306844/1‑81 (MQ=255)
                        cGCTATGCCGACGCACCAGCCATGCATGTCGCGCATCGCTCCCATGTCATCAATATGCTTGATGGTGATGCATTACGCCgt                                               >  2:306842/1‑81 (MQ=255)
                         gCTATGCCGACGCACCAGCCATGCATGTCGCGCATCGCTCCCATGTCATCAATATGCTTGATGGTGATGCATTACGCCgt                                               <  2:306800/80‑1 (MQ=255)
                               ccGACGCACCAGCCATGCATGTCGCGCATCGCTCCCATGTCATCAATATGCTTGATGGTGATGCATTACGCCGTGTGGTTg                                        <  2:306801/81‑1 (MQ=255)
                                    gCACCAGCCATGCATGTCGCGCATCGCTCCCATGTCATCAATATGCTTGATGGTGATGCATTACGCCGTGTGGTTGAACTg                                   <  1:306802/81‑1 (MQ=255)
                                           ccATGCATGTCGCGCATCGCTCCCATGTCATCAATATGCTTGATGGTGATGCATTACGCCGTGTGGTTGAACTGGAAAAAc                            >  2:306845/1‑81 (MQ=255)
                                            catgcatgTCGCGCATCGCTCCCATGTCATCAATATGCTTGATGGTGATGCATTACGCCGTGTGGTTGAACTGGAAAAAc                            >  2:306835/1‑80 (MQ=255)
                                                 atgTCGCGCATCGCTCCCATGTCATCAATATGCTTGATGGTGATGCATTACGCCGTGTGGTTGAACTGGAAAAACCACAt                       >  2:306841/1‑80 (MQ=255)
                                                    tCGCGCATCGCTCCCATGTCATCAATATGCTTGATGGTGATGCATTACGCCGTGTGGTTGAACTGGAAAAACCACATtata                   <  1:306804/81‑1 (MQ=255)
                                                    tCGCGCATCGCTCCCATGTCATCAATATGCTTGATGGTGATGCATTACGCCGTGTGGTTGAACTGGAAAAACCACATtat                    <  2:306803/80‑1 (MQ=255)
                                                      gcgcATCGCTCCCATGTCATCAATATGCTTGATGGTGATGCATTACGCCGTGTGGTTGAACTGGAAAAACCACATTATATc                 <  1:306805/81‑1 (MQ=255)
                                                        gcATCGCTCCCATGTCATCAATATGCTTGATGGTGATGCATTACGCCGTGTGGTTGAACTGGAAAAACCACATTATATCGt               <  1:306806/81‑1 (MQ=255)
                                                             gCTCCCATGTCATCAATATGCTTGATGGTGATGCATTACGCCGTGTGGTTGAACTGGAAAAACCACATTATATCGTGCCgg          <  2:306807/81‑1 (MQ=255)
                                                                 ccATGTCATCAATATGCTTGATGGTGATGCATTACGCCGTGTGGTTGAACTGGAAAAACCACATTATATCGTGCCGgag        <  1:306808/79‑1 (MQ=255)
                                                                   aTGTCATCAATATGCTTGATGGTGATGCATTACGCCGTGTGGTTGAACTGGAAAAACCACATTATATCGTGCCGGAGATc     >  1:306848/1‑80 (MQ=255)
                                                                   aTGTCATCAATATGCTTGATGGTGATGCATTACGCCGTGTGGTTGAACTGGAAAAACCACATTATATCGTGCCGGAGATCg    <  2:306809/81‑1 (MQ=255)
                                                                      tcatcaATATGCTTGATGGTGATGCATTACGCCGTGTGGTTGAACTGGAAAAACCACATTATATCGTGCCGGAGATCGaa  <  2:306810/80‑1 (MQ=255)
                                                                          |                                                                           
GGCGTAGAGGTGATTGCCGTCGATCGCTATGCCGACGCACCAGCCATGCATGTCGCGCATCGCTCCCATGTCATTAATATGCTTGATGGTGATGCATTACGCCGTGTGGTTGAACTGGAAAAACCACATTATATCGTGCCGGAGATCGAA  >  NC_000913/1930983‑1931132

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 31 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: