Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_007793 311,275 C→T P156L (CCG→CTG)  SAUSA300_RS01380 → hypothetical protein

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_007793311,2750CT100.0% 30.8 / NA 12P156L (CCG→CTG) SAUSA300_RS01380hypothetical protein
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base T (8/4);  total (8/4)

TTTTTAGAGAGAAAATGGTAGGTGAAGGCTTAGCAATCAAAGCTCATGAAGAATCCAAAGTAATCGCACCGTTCAATGGTTTAATATCTATGATTGTACCAACTAAGCATGCAGTTGGTATTCAATCAGAAGACGGTGTGGACATAGTCATTCATATTGGCTTGA  >  NC_007793/311206‑311370
                                                                     |                                                                                               
tttttAGAGAGAAAATGGTAGGTGAAGGCTTAGCAATCAAAGCTCATGAAGAATCCAAAGTAATCGCACTGTTCAATGGTTTAATATCTATGATTGTAcc                                                                   <  1:2901491/100‑1 (MQ=255)
        gagaAAATGGTAGGTGAAGGCTTAGCAATCAAAGCTCATGAAGAATCCAAAGTAATCGCACTGTTCAATGGTTTAATATCTATGATTGTACCAACTAAGc                                                           <  1:3969483/100‑1 (MQ=255)
           aaaaTGGTAGGTGAAGGCTTAGCAATCAAAGCTCATGAAGAATCCAAAGTAATCGCACTGTTCAATGGTTTAATATCTATGATTGTACCAACTAAGCATg                                                        <  1:5291283/100‑1 (MQ=255)
             caTGGTAGGTGAAGGCTTAGCAATCAAAGCTCATGAAGAATCCAAAGTAATCGCACTGTTCAATGGTTTAATATCTATGATTGTACCAACTAAGCATGCa                                                      >  1:5591580/2‑100 (MQ=255)
                ggTAGGTGAAGGCTTAGCAATCAAAGCTCATGAAGAATCCAAAGTAATCGCACTGTTCAATGGTTTAATATCTATGATTGTACCAACTAAGCATGCAGtt                                                   >  1:4543831/1‑100 (MQ=255)
                   aGGTGAAGGCTTAGCAATCAAAGCTCATGAAGAATCCAAAGTAATCGCACTGTTCAATGGTTTAATATCTATGATTGTACCAACTAAGCATGCAGTTGGt                                                >  1:2663714/1‑100 (MQ=255)
                              tAGCAATCAAAGCTCATGAAGAATCCAAAGTAATCGCACTGTTCAATGGTTTAATATCTCTGATTGTACCAACTAAGCATGCAGTTGGTATTCAATCaga                                     >  1:3724996/1‑100 (MQ=255)
                                        tgCTCATGAAGAATCCAAAGTAATCGCACTGTTCAATGGTTTAATATCTATGATTGTACCAACTAAGCATGCAGTTGGTATTCAATCAGAAGACGGtgtg                           >  1:4034016/2‑100 (MQ=255)
                                        aGCTCATGAAGAATCCAAAGTAATCGCACTGTTCAATGGTTTAATATCTATGATTGTACCAACTAAGCATGCAGTTGGTATTCAATCAGAAGACGGtgtg                           >  1:3140777/1‑100 (MQ=255)
                                         ccTCATGAAGAATCCAAAGTAATCGCACTGTTCAATGGTTTAATATCTATGATTGTACCAACTAAGCATGCAGTTGGTATTCAATCAGAAGACGGTGTgg                          >  1:3799379/2‑100 (MQ=255)
                                            cATGAAGAATCCAAAGTAATCGCACTGTTCAATGGTTTAATATCTATGATTGTACCAACTAAGCATGCAGTTGGTATTCAATCAGAAGACGGTGTGGACa                       >  1:1521881/1‑100 (MQ=255)
                                                                 gCACTGTTCAATGGTTTAATATCTATGATTGTACCAACTAAGCATGCAGTTGGTATTCAATCAGAAGACGGTGTGGACATAGTCATTCATATTGGCGTgg  <  1:3899543/100‑2 (MQ=255)
                                                                     |                                                                                               
TTTTTAGAGAGAAAATGGTAGGTGAAGGCTTAGCAATCAAAGCTCATGAAGAATCCAAAGTAATCGCACCGTTCAATGGTTTAATATCTATGATTGTACCAACTAAGCATGCAGTTGGTATTCAATCAGAAGACGGTGTGGACATAGTCATTCATATTGGCTTGA  >  NC_007793/311206‑311370

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap: ‑    Deleted base: ‑