Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,347,878 T→C Q345Q (CAA→CAG rnb ← RNase II

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,347,8780TC100.0% 72.6 / NA 22Q345Q (CAA→CAGrnbRNase II
Reads supporting (aligned to +/- strand):  ref base T (0/0);  new base C (12/10);  total (12/10)

TTTCACCGAGAATAAAGCGGTAATCCGGGCGATCTTTAAACACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGTTGGCAAATTTGCGCTAGCAAACGGACTTGTTCGGCAATTGCTTCACTTTCAGGCTGCCAGTCACCGGTATTTTC  >  NC_000913/1347802‑1347952
                                                                            |                                                                          
tttCACCGAGAATAAAGCGGTAATCCGGGCGATCTTTAAACACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTg                                                                          <  2:260072/79‑1 (MQ=255)
  tCACCGAGAATAAAGCGGTAATCCGGGCGATCTTTAAACACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTGGCa                                                                       <  1:260073/80‑1 (MQ=255)
    aCCGAGAATAAAGCGGTAATCCGGGCGATCTTTAAACACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTGGCaaa                                                                     <  2:260074/80‑1 (MQ=255)
       gagaATAAAGCGGTAATCCGGGCGATCTTTAAACACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTGGCAAATTTg                                                                 >  2:260102/1‑81 (MQ=255)
        agaATAAAGCGGTAATCCGGGCGATCTTTAAACACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTGGCAAATTTgc                                                                <  1:260075/81‑1 (MQ=255)
                 cGGTAATCCGGGCGATCTTTAAACACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTGGCAAATTTGCGCTAGCaaa                                                       >  2:260114/1‑81 (MQ=255)
                     aaTCCGGGCGATCTTTAAACACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTGGCAAATTTGCGCTAGCAAACGGa                                                   >  2:260117/1‑81 (MQ=255)
                      aTCCGGGCGATCTTTAAACACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTGGCAAATTTGCGCTAGCAAACGGAc                                                  >  2:260100/1‑81 (MQ=255)
                            gCGATCTTTAAACACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTGGCAAATTTGCGCTAGCAAACGGACTTGTTc                                            >  2:260110/1‑81 (MQ=255)
                            gCGATCTTTAAACACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTGGCAAATTTGCGCTAGCAAACGGACTTGTTc                                            <  1:260076/81‑1 (MQ=255)
                             cGATCTTTAAACACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTGGCAAATTTGCGCTAGCAAACGGACTTGTTCg                                           <  1:260077/81‑1 (MQ=255)
                                tCTTTAAACACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTGGCAAATTTGCGCTAGCAAACGGACTTGTTCGGc                                         >  2:260106/1‑80 (MQ=255)
                                    tAAACACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTGGCAAATTTGCGCTAGCAAACGGACTTGTTCGGCAAtt                                     <  2:260078/80‑1 (MQ=255)
                                      aaCACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTGGCAAATTTGCGCTAGCAAACGGACTTGTTCGGCAATTGc                                   <  1:260079/80‑1 (MQ=255)
                                      aaCACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTGGCAAATTTGCGCTAGCAAACGGACTTGTTCGGCAATTGCt                                  >  2:260107/1‑81 (MQ=255)
                                       acacCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTGGCAAATTTGCGCTAGCAAACGGACTTGTTCGGCAATTGCtt                                 >  2:260115/1‑81 (MQ=255)
                                          ccAGTGCGTGGTTATGACGCCACTCGCCGCGGCGCTGGCAAATTTGCGCTAGCAAACGGACTTGTTCGGCAATTGCTTCAc                              <  2:260080/81‑1 (MQ=255)
                                                 gTGGTTATGACGCCACTCGCCGCGGCGCTGGCAAATTTGCGCTAGCAAACGGACTTGTTCGGCAATTGCTTCACTTTCAgg                       >  1:260112/1‑81 (MQ=255)
                                                   ggTTATGACGCCACTCGCCGCGGCGCTGGCAAATTTGCGCTAGCAAACGGACTTGTTCGGCAATTGCTTCACTTTCAGGCt                     >  2:260101/1‑81 (MQ=255)
                                                              cACTCGCCGCGGCGCTGGCAAATTTGCGCTAGCAAACGGACTTGTTCGGCAATTGCTTCACTTTCAGGCTGCCAGTCACCg          <  2:260081/81‑1 (MQ=255)
                                                                  cgccgcGGCGCTGGCAAATTTGCGCTAGCAAACGGACTTGTTCGGCAATTGCTTCACTTTCAGGCTGCCAGTCACCGGTAt      >  1:260111/1‑81 (MQ=255)
                                                                       cggcgCTGGCAAATTTGCGCTAGCAAACGGACTTGTTCGGCAATTGCTTCACTTTCAGGCTGCCAGTCACCGGTATTTTc  >  1:260108/1‑80 (MQ=255)
                                                                            |                                                                          
TTTCACCGAGAATAAAGCGGTAATCCGGGCGATCTTTAAACACCAGTGCGTGGTTATGACGCCACTCGCCGCGGCGTTGGCAAATTTGCGCTAGCAAACGGACTTGTTCGGCAATTGCTTCACTTTCAGGCTGCCAGTCACCGGTATTTTC  >  NC_000913/1347802‑1347952

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 35 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: