Predicted mutation
evidence	seq id	position	mutation	annotation	gene	description
RA	NC_000913	1,707,546	C→T	L210F (CTT→TTT)	rsxC →	SoxR [2Fe‑2S] reducing system protein RsxC

Read alignment evidence...
	seq id	position		ref	new	freq	score (cons/poly)	reads	annotation	genes	product
*	NC_000913	1,707,546	0	C	T	100.0%	24.1 / NA	10	L210F (CTT→TTT)	rsxC	SoxR [2Fe‑2S] reducing system protein RsxC
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base T (5/5);  total (5/5)

GTGTTGCCGGGCTGGGCGGTGCAGGATTCCCGACAGGCGTTAAATTGCAGGGTGGCGGAGATAAGATTGAAACGTT‑GATTATCAACGCGGCTGAGTGCGAGCCGTACATTACCGCCGATGACCGTTTGATGCAGGATTGCGCGGCTCAGGTCGTAGAGGGTATTCGCATTCTTGCGCATATTCTGCAGCCACGCGAAATTCTTATCGGCATTGAAGATAACAAACCGCAGGCGATTTCCATGCTGCGCGCGGTGCTGGCGGACTCTAACGATATTTCTCTGCGGGTGATTCCAACCAAATATCCTTCTGGCGGTGCTAAACAATTAACCTACATTCTGACCGGGAAGC  >  NC_000913/1707346‑1707693                                                                                                                                                                                                          |                                                                                                                                                    gtgtTGCCGGGCTGGGCGGTGCAGGATTCCCGACAGGCGTTAAATTGCAGGGTGGCGGAGATACGATTGAAACGTT‑GATTATCAACGCGGCTGAGTGCGAGCCGTACATTACCGCCGATGACCGTTTGATGCAGGCTTGCGCGGCTCAGGTCGTAGAGGGTATTCGCATTCTTGCGCATATTCTGCAGCCACGCGAAATTTTTATCGGCATTGAAGATAACAAACCGCAGGCGATTTCCATGCTGcgcgcg                                                                                                   >  1:282488/1‑251 (MQ=255)              nggCGGTGCAGGATTCCCGACAGGCGTTAAATTGCAGGGTGGCGGAGATAAGATTGAAACGTT‑GATTATCAACGCGGCTGAGTGCGAGCCGTACATTACCGCCGATGACCGTTTGATGCAGGATTGCGCGGCTCAGGTCGTAGAGGGTATTCGCATTCTTGCGCATATTCTGCAGCCACGCGAAATTTTTATCGGCATTGAAGATAACAAACCGCAGGCGATTTCCATGCTGCGCGCGGTGCTGGCGGAct                                                                                      >  1:85157/2‑251 (MQ=255)                   gTGCAGGATTCCCGACAGGCGTTAAATTGCAGGGTGGCGGAGATAAGATTGAACCGTT‑GCTTATCAACGCGGTTGAGTGCGAGCCGTACATTAACGACGATCACCGTTTGACGCAGGATTGCGCCGCTCAGGTCGCAGAGGGTATTCGCATTCTTGCGCATATTCTGCAGCCACGCGAAATTTTTATc                                                                                                                                                >  1:208735/1‑188 (MQ=255)                                  caggatttatatggCAGGGTGGCGGAAATAATATTGAA‑CGTTTGATTATCAACGCGGTTGATTGCGTGCCGTACATTACCGCCGATGACCGTTTGATGCAGGATTGCGCAGCTCAGGTCGTAGAGGGTATTCTCATTCTTGCGCATATTCTGCAGCCACGCGAAATTTTTATCGGCATTGAAGATAACAAACCGCATGCGATTTCCATGCTGCGCGCGGTGCTGGCGGACTCTAACGATATTTCTCTGctg                                                                  <  1:230781/238‑3 (MQ=255)                                  cAGGCGTTAAATTGCAGGGTGGCGGAGATAAGATTGAAGCGTT‑GATTATCACCGCGGCTGAGTGCGGGCCTTACATTACCGCCGATGACCGTTTGATGCAGGATTGCGCGGCTCAGGTCGTAGAGGGTATTCGCATTCTTGCGCATATTCTGCAGCCACGCGAAATTTTTATCGGCATTGAAGATAACAAACCGCAGGCGATTTCCATGCTGCGCGCGGTGCTGGCGGACTCTAACGATATTTCTCTGCgg                                                                  <  1:230787/251‑1 (MQ=255)                                                                                                                                                                      cGCATTCTTGCGCATCTTCTGCAGCCACGCGAAATTTTTATCGGCATTGAAGATAACAAACCGCAGGCGATTTCCATGCTGCGCGCGGTGCTGGCGGACTCTAACGATATTTctct                                                                      >  1:257034/1‑116 (MQ=255)                                                                                                                                                                       gCATTCTTGCGCATATTCTGCAGCCACGCGAAATTTTTATCGGCATTGAAGATAACAAACCGCAGGCGATTTCCATGCTGCGCGCGGTGCTGGCGGACTCTAACGATATTTCTCTGCGGGTGATTCCAACCAAATATcc                                              <  1:188341/139‑1 (MQ=255)                                                                                                                                                                       gCATTCTTGCGCATATTCTGCAGCCACGCGAAATTTTTAGCGGCATTGAAGATAACAAACCGCAGGCGATTTCCATGCTGCGCGCGGTGCTGGCGGACTCTAACGATATTTCTCTGCGGGTGATTCCAACCAAATATCCTTCTGGCGGTGCTAAACAATTAACCTAc                  <  1:289628/167‑1 (MQ=255)                                                                                                                                                                                                     aaaTTTTTATCGGCATTGAAGATAACAAACCGCAGGCGATTTCCATGCTGCGCGCGGTGCTGGCGGACTCTAACGATATTTCTCTGCGGGTGATTCCAACCAAATATCCTTCTGGCGGTGCTAAACAATTAACNTACNNNNNGann         >  2:196651/1‑144 (MQ=255)                                                                                                                                                                                                     aaaTTTTTATCGGCATTGAAGATAACAAACCGCAGGCGATTTCCATGCTGCGCGCGGTGCTGGCGGACTCTAACGATATTTCTCTGCGGGTGATTCCAACCAAATATCCTTCTGGCGGTGCTAAACAATTAACCTACATTCTGACCGGGAAgn  <  1:196651/153‑2 (MQ=255)                                                                                                                                                                                                          |                                                                                                                                                    GTGTTGCCGGGCTGGGCGGTGCAGGATTCCCGACAGGCGTTAAATTGCAGGGTGGCGGAGATAAGATTGAAACGTT‑GATTATCAACGCGGCTGAGTGCGAGCCGTACATTACCGCCGATGACCGTTTGATGCAGGATTGCGCGGCTCAGGTCGTAGAGGGTATTCGCATTCTTGCGCATATTCTGCAGCCACGCGAAATTCTTATCGGCATTGAAGATAACAAACCGCAGGCGATTTCCATGCTGCGCGCGGTGCTGGCGGACTCTAACGATATTTCTCTGCGGGTGATTCCAACCAAATATCCTTCTGGCGGTGCTAAACAATTAACCTACATTCTGACCGGGAAGC  >  NC_000913/1707346‑1707693

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 31 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap: ‑    Deleted base: ‑