Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,240,439 C→T V60V (GTC→GTT
D545N (GAC→AAC) 
ymgM →
cvrA ←
protein YmgM
putative K(+):H(+) antiporter

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,240,4390CT100.0% 72.8 / NA 19V60V (GTC→GTT
D545N (GAC→AAC) 
ymgM
cvrA
protein YmgM
putative K(+):H(+) antiporter
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base T (6/13);  total (6/13)

TTCTCGGCCACCGTCCAGATCATCCCGGCAAACTCTACCTGGTCACCGACAACCGGTGCCGCGCCTAACAACTGCTGGACAATTTC  >  NC_000913/1240396‑1240481
                                           |                                          
ttctCGGCCACCGTCCAGATCATCCCGGCAAACTCTACCTGGTTACCGa                                       >  1:385055/1‑49 (MQ=255)
  ctcGGCCACCGTCCAGATCATCCCGGCAAACTCTACCTGGTTACCGAc                                      >  1:1416153/1‑48 (MQ=255)
    cGGCCACCGTCCAGATCATCCCGGCAAACTCTACCTGGTTACCGACAAc                                   >  1:1219413/1‑49 (MQ=255)
     ggCCACCGTCCAGATCATCCCGGCAAACTCTACCTGGTTACCGACAAc                                   <  1:2765279/48‑1 (MQ=255)
      gCCACCGTCCAGATCATCCCGGCAAACTCTACCTGGTTACCGACAACCg                                 <  1:1186086/49‑1 (MQ=255)
      gCCACCGTCCAGATCATCCCGGCAAACTCTACCTGGTTACCGACAACCg                                 <  1:2636351/49‑1 (MQ=255)
        cACCGTCCAGATCATCCCGGCAAACTCTACCTGGTTACCGACAACCGGt                               <  1:485163/49‑1 (MQ=255)
            gTCCAGATCATCCCGGCAAACTCTACCTGGTTACCGACAACCGGTGCcg                           <  1:1496592/49‑1 (MQ=255)
              ccAGATCATCCCGGCAAACTCTACCTGGTTACCGACAACCGGTGCcgcg                         >  1:2790531/1‑49 (MQ=255)
                aGATCATCCCGGCAAACTCTACCTGGTTACCGACAACCGGTGCCGCGcc                       <  1:2362121/49‑1 (MQ=255)
                 gATCATCCCGGCAAACTCTACCTGGTTACCGACAACCGGTGCCGCGCCt                      <  1:2736871/49‑1 (MQ=255)
                  atcatcCCGGCAAACTCTACCTGGTTACCGACAACCGGTGCCGCGCCt                      >  1:1319895/1‑48 (MQ=255)
                     atcCCGGCAAACTCTACCTGGTTACCGACAACCGGTGCCGCGCCTaaca                  <  1:452227/49‑1 (MQ=255)
                      tcCCGGCAAACTCTACCTGGTTACCGACAACCGGTGCCGCGCCTaacaa                 <  1:293459/49‑1 (MQ=255)
                         cGGCAAACTCTACCTGGTTACCGACAACCGGTGCCGCGCCTAACAActg              <  1:1526155/49‑1 (MQ=255)
                          ggCAAACTCTACCTGGTTACCGACAACCGGTGCCGCGCCTAACAActgc             >  1:1047688/1‑49 (MQ=255)
                            cAAACTCTACCTGGTTACCGACAACCGGTGCCGCGCCTAACAActgctg           <  1:263603/49‑1 (MQ=255)
                                ctctACCTGGTTACCGACAACCGGTGCCGCGCCTAACAACTGCTGGACa       <  1:408554/49‑1 (MQ=255)
                                     ccTGGTTACCGACAACCGGTGCCGCGCCTAACAACTGCTGGACAATTTc  <  1:275427/49‑1 (MQ=255)
                                           |                                          
TTCTCGGCCACCGTCCAGATCATCCCGGCAAACTCTACCTGGTCACCGACAACCGGTGCCGCGCCTAACAACTGCTGGACAATTTC  >  NC_000913/1240396‑1240481

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: