Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_007793 2,094,634 G→A P216P (CCC→CCT)  SAUSA300_RS10580 ← hypothetical protein

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0077932,094,6340GA100.0% 33.3 / NA 13P216P (CCC→CCT) SAUSA300_RS10580hypothetical protein
Reads supporting (aligned to +/- strand):  ref base G (0/0);  new base A (7/6);  total (7/6)

TATCCCCCAAATATAGCGCATAGGTAGGTTGAATTGACTTTGCGCTTCGTCATCTGTCACAACTAGCTCTAAACGCTTTCCTTTGTCATTTTCGGGTCCCACAGCAATTAATGCTGTTTTGATTTCTGACATATCAATCTTCCTAGTTAACCCAACCAAATCTTTACCATACTCAATTTCTTTACCTT  >  NC_007793/2094541‑2094728
                                                                                             |                                                                                              
tatCCCCCAAATATAGCGCATAGGTAGGTTGAATTGACTTTGCGCTTCGTCATCTGTCACAACTAGCTCTAAACGCTTCCCTTTGTCATTTTCAGGTccc                                                                                          <  1:5358958/100‑1 (MQ=255)
      ccAAATATAGCGCATAGGTAGGTTGAATTGACTTTGCGCTTCGTCATCTGTCACAACTAGCTCTAAACGCTTCCCTTTGTCATTTTCAGGTCCCACAGCa                                                                                    <  1:3144824/100‑1 (MQ=255)
      ccAAATATAGCGCATAGGTAGGTTGAATTGACTTTGCGCTTCGTCATCTGTCACAACTAGCTCTAAACGCTTCCCTTTGTCATTTTCAGGTCCCACAGCa                                                                                    >  1:5344354/1‑100 (MQ=255)
           tcaggtgcATAGGTAGGTTGAATTGACTTTGCGCTTCGTCATCTGTCACAACTAGCTCTAAACGCTTCCCTTTGTCATTTTCAGGTCCCACAGCAATTaa                                                                               >  1:2473199/7‑100 (MQ=255)
                                               cgatctCTGTCACAACTAGCTCTAAACGCTTCCCTTTGTCATTTTCAGGTCCCACAGCAATTAATGCTGTTTTGATTTCTGACATATCAATCTTCCTAGt                                           <  1:5592390/95‑1 (MQ=255)
                                                                      aaaCGCTTCCCTTTGTCATTTTCAGGTCCCACAGCAATTAATGCTGTTTTGATTTCTGACATATCAATCTTCCTAGTTAACCCGACTAAATCTTTACCAt                    >  1:3390532/1‑100 (MQ=255)
                                                                      aaaCGCTTCCCTTTGTCATTTTCAGGTCCCACAGCAATTAATGCTGTTTTGATTTCTGACATATCAATCTTCCTAGTTAACCCGACTAAATCTTTACCAt                    <  1:4182152/100‑1 (MQ=255)
                                                                      aaaCGCTTCCCTTTGTCATTTTCAGATCCCACAGCAATTAATGCTGTTTTGATTTCTGACATATCAATCTTCCTAGTTAACCCGACTAAATCTTTACCAt                    <  1:4751712/100‑1 (MQ=255)
                                                                              ccctacgTCATTTTCAGGTCCCACAGCAATTAATGCTGTTTTGATTTCTGACATATCAATCTTCCTAGTTAACCCGACTAAATCTTTACCATATTCAAtt            >  1:2573124/7‑100 (MQ=255)
                                                                              cccTTTGTCATTTTCAGGTCCCACAGCAATTAATGCTGTTTTGATTTCTGACATATCAATCTTCCTAGTTAACCCGACTAAATCTTTACCATATTCAAtt            >  1:3159980/2‑100 (MQ=255)
                                                                              cccTTTGTCATTTTCAGGTCCCACAGCAATTAATGCTGTTTTGATTTCTGACATATCAATCTTCCTAGTTAACCCGACTAAATCTTTACCATATTCAAtt            >  1:322442/2‑100 (MQ=255)
                                                                              cccTTTGTCATTTTCAGGTCCCACAGCAATTAATGCTGTTTTGATTTCTGACATATCAATCTTCCTAGTTAACCCGACTAAATCTTTACCATATTCAAtt            >  1:3566925/2‑100 (MQ=255)
                                                                                        ttttCAGGTCCCACAGCAATTAATGCTGTTTTGATTTCTGACATATCAATCTTCCTAGTTAACCCGACTAAATCTTTACCATATTCAATTTCTTTACCtt  <  1:2438474/100‑1 (MQ=255)
                                                                                             |                                                                                              
TATCCCCCAAATATAGCGCATAGGTAGGTTGAATTGACTTTGCGCTTCGTCATCTGTCACAACTAGCTCTAAACGCTTTCCTTTGTCATTTTCGGGTCCCACAGCAATTAATGCTGTTTTGATTTCTGACATATCAATCTTCCTAGTTAACCCAACCAAATCTTTACCATACTCAATTTCTTTACCTT  >  NC_007793/2094541‑2094728

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap: ‑    Deleted base: ‑