Predicted mutation
evidence seq id position mutation annotation gene description
RA CP009974 1,154,311 T→C T337T (ACT→ACC RPPX_05115 → hypothetical protein

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*CP0099741,154,3110TC100.0% 30.7 / NA 17T337T (ACT→ACCRPPX_05115hypothetical protein
Reads supporting (aligned to +/- strand):  ref base T (0/0);  new base C (10/7);  total (10/7)

GTTCAGCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACTGACCTGGCCCT  >  CP009974/1154164‑1154322
                                                                                                                                                   |           
gTTCAGCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACcgaccgac          >  1:4037106/1‑151 (MQ=25)
gTTCAGCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACcgaccgac          >  2:3595361/1‑151 (MQ=25)
gTTCAGCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACcgaccgac          >  2:2365730/1‑151 (MQ=25)
 ttCAGCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTCCAGCCCCTGAACAACCgaccgacc         >  2:4127730/1‑151 (MQ=25)
 ttCAGCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCgaccgacc         >  1:352403/1‑151 (MQ=25)
  tCAGCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACCGAcct        >  1:2326420/1‑151 (MQ=21)
   cAGCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACGTCACGGCACCGGACGTCGACACCCCTGATACTACATCCCCTGAACAAACGACCGAcctg       >  2:6234793/1‑151 (MQ=255)
   cAGCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACCGAcctg       <  1:2594441/151‑1 (MQ=18)
   cAGCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACCGAcctg       >  2:5522587/1‑151 (MQ=18)
   cAGCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACCGAcctg       <  2:1310033/151‑1 (MQ=18)
   cAGCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACCGAcctg       >  2:2916973/1‑151 (MQ=18)
    aGCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACCGAcctgg      >  2:728865/1‑151 (MQ=17)
    aGCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACCGAcctgg      >  1:139443/1‑151 (MQ=17)
     gCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACCGAcctggc     <  1:714179/151‑1 (MQ=14)
     gCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACCGAcctggc     >  2:5671255/1‑151 (MQ=14)
       aTTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACCGAcctggccc   <  1:5991257/151‑1 (MQ=14)
       aTTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACCGAcctggccc   >  1:5965405/1‑151 (MQ=14)
       aTTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACCGAcctggccc   >  2:6537186/1‑151 (MQ=14)
       aTTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACCGAcctggccc   >  1:3208927/1‑151 (MQ=14)
       aTTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGGTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACCGAcctggccc   <  2:4157575/151‑1 (MQ=14)
        ttACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACCGAcctggccct  <  2:1408737/151‑1 (MQ=11)
        ttACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACCGAcctggccct  <  1:4362525/151‑1 (MQ=11)
                                                                                                                                                   |           
GTTCAGCATTACCCTGCAACCGCCACAAAGCGACGGCCAGGCCCTGGAGGTCAGCGCCGCAGATGCGGCAGGCAATAGCTCGCCAGTTGCCAACATCACGGCACCGGACGTCGACACCCCTGATACTACAGCCCCTGAACAACCGACTGACCTGGCCCT  >  CP009974/1154164‑1154322

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: