Predicted mutation
evidence	seq id	position	mutation	annotation	gene	description
RA	NC_000913	4,291,502	C→A	intergenic (+70/‑10)	nrfD → / → nrfE	putative menaquinol‑cytochrome c reductase subunit NrfD/putative cytochrome c‑type biogenesis protein NrfE

Read alignment evidence...
	seq id	position		ref	new	freq	score (cons/poly)	reads	annotation	genes	product
*	NC_000913	4,291,502	0	C	A	100.0%	45.4 / NA	14	intergenic (+70/‑10)	nrfD/nrfE	putative menaquinol‑cytochrome c reductase subunit NrfD/putative cytochrome c‑type biogenesis protein NrfE
Reads supporting (aligned to +/- strand):  ref base C (0/0);  new base A (5/9);  total (5/9)

AGTCTGGTCGGCGTGTTGATGCTGCGCTTTTTCATTCTCTACGCCGGACAGTTGACGGTGGCGTAAGCCAGAAAAGAGGTGGTTTCTGGACGTATTCCTTCCTGAAGTCGGTTTTCTGGCGTTGTTGTTAAGTCTCGGGGTCAACGTGTTGACCCCGTTGACGGCCTTCGCGGGAGTGCGGTTGCGCTGGCCTGCCATGATGCGACTCACTTGCATCGGCATTCTGGCGCAGTTCGCGCTCCTGCTGCTCGCCTTTGGCG  >  NC_000913/4291367‑4291626                                                                                                                                        |                                                                                                                             aGTCTGGTCGGCGTGTTGATGCTGCGCTTTTTCATTCTCTACGCCGGACAGTTGACGGTGGCGTAAGCCAGAAAAGAGGTGGTTTCTGGACGTATTCCTTCCTGAAGTCGGTTTTCTGGCGTTGTTGTTAAGTCTAgggg                                                                                                                          <  1:327068/140‑1 (MQ=255) aGTCTGGTCGGCGTGTTGATGCTGCGCTTTTTCATTCTCTACGCCGGACAGTTGACGGTGGCGTAAGCCAGAAAAGAGGTGGTTTCTGGACGTATTCCTTCCTGAAGTCGGTTTTCTGGCGTTGTTGTTAAGTCTAgggg                                                                                                                          <  1:81983/140‑1 (MQ=255)               gtTGATGCTGCGCTTTTTCATTCTCTACGCCGGACAGTTGACGGTGGCGTAAGCCAGAAAAGAGGTGGTTTCTGGACGTATTCCTTCCTGAAGTCGGTTTTCTGGCGTTGTTGTTAAGTCTAGGGGTCAACGTGTTGAcc                                                                                                            <  1:127080/140‑1 (MQ=255)                ttGATGCTGCGCTTTTTCATTCTCTACGCCGGACAGTTGACGGTGGCGTAAGCCAGAAAAGAGGTGGTTTCTGGACGTATTCCTTCCTGAAGTCGGTTTTCTGGCGTTGTTGTTAAGTCTAGGGGTCAACGTGTTGAccc                                                                                                           <  2:34467/140‑1 (MQ=255)                      ctgcGCTTTTTCATTCTCTACGCCGGACAGTTGACGGTGGCGTAAGCCAGAAAAGAGGTGGTTTCTGGACGTATTCCTTCCTGAAGTCGGTTTTCTGGCGTTGTTGTTAAGTCTAGGGGTCAACGTGTTGACCCCGTTGa                                                                                                     <  2:89858/140‑1 (MQ=255)                                     ctctACGCCGGACAGTTGACGGTGGCGTAAGCCAGAAAAGAGGTGGTTTCTGGACGTATTCCTTCCTGAAGTCGGTTTTCTGGCGTTGTTGTTAAGTCTAGGGGTCAACGTGTTGACCCCGTTGACGGCCTTCGCGGGAg                                                                                      <  2:295253/140‑1 (MQ=255)                                                  aGTTGACGGTGGCGTAAGCCAGAAAAGAGGTGGTTTCTGGACGTATTCCTTCCTGAAGTCGGTTTTCTGGCGTTGTTGTTAAGTCTAGGGGTCAACGTGTTGACCCCGTTGACGGCCTTCGCGGGAGTGCGGTTgcg                                                                            <  1:163006/137‑1 (MQ=255)                                                  aGTTGACGGTGGCGTAAGCCAGAAAAGAGGTGGTTTCTGGACGTATTCCTTCCTGAAGTCGGTTTTCTGGCGTTGTTGTTAAGTCTAGGGGTCAACGTGTTGACCCCGTTGACGGCCTTCGCGGGAGTGCGGTTgcg                                                                            >  2:163006/1‑137 (MQ=255)                                                              cGTAAGCCAGAAAAGAGGTGGTTTCTGGACGTATTCCTTCCTGAAGTCGGTTTTCTGGCGTTGTTGTTAAGTCTAGGGGTCAACGTGTTGACCCCGTTGACGGCCTTCGCGGGAGTGCGGTTGCGCTGGCCTGCCatgat                                                             >  2:24812/1‑140 (MQ=255)                                                                             agGTGGTTTCTGGACGTATTCCTTCCTGAAGTCGGTTTTCTGGCGTTGTTGTTAAGTCTAGGGGTCAACGTGTTGACCCCGTTGACGGCCTTCGCGGGAGTGCGGTTGCGCTGGCCTGCCATGATGCGACTCACTTGCAt                                              >  2:259288/1‑140 (MQ=255)                                                                                                 ccttcctGAAGTCGGTTTTCTGGCGTTGTTGTTAAGTCTAGGGGTCAACGTGTTGACCCCGTTGACGGCCTTCGCGGGAGTGCGGTTGCGCTGGCCTGCCATGATGCGACTCACTTGCATCGGCATTCTGGCGCAGTTcg                          <  1:24812/140‑1 (MQ=255)                                                                                                    tcctGAAGTCGGTTTTCTGGCGTTGTTGTTAAGTCTAGGGGTCAACGTGTTGACCCCGTTGACGGCCTTCGCGGGAGTGCGGTTGCGCTGGCCTGCCATGATGCGACTCACTTGCATCGGCATTCTGGCGCAGTTCgcgc                       >  1:119375/1‑140 (MQ=255)                                                                                                              ggTTTTCTGGCGTTGTTGTTAAGTCTAGGGGTCAACGTGTTGACCCCGTTGACGGCCTTCGCGGGAGTGCGGTTGCGCTGGCCTGCCATGATGCGACTCACTTGCATCGGCATTCTGGCGCAGTTCGCGCTCCTgctgct             >  2:62613/1‑140 (MQ=255)                                                                                                                         gttgttgttAAGTCTAGGGGTCAACGTGTTGACCCCGTTGACGGCCTTCGCGGGAGTGCGGTTGCGCTGGCCTGCCATGATGCGACTCACTTGCATCGGCATTCTGGCGCAGTTCGCGCTCCTGCTGCTCGCCTTTGGCg  <  2:119375/140‑1 (MQ=255)                                                                                                                                        |                                                                                                                             AGTCTGGTCGGCGTGTTGATGCTGCGCTTTTTCATTCTCTACGCCGGACAGTTGACGGTGGCGTAAGCCAGAAAAGAGGTGGTTTCTGGACGTATTCCTTCCTGAAGTCGGTTTTCTGGCGTTGTTGTTAAGTCTCGGGGTCAACGTGTTGACCCCGTTGACGGCCTTCGCGGGAGTGCGGTTGCGCTGGCCTGCCATGATGCGACTCACTTGCATCGGCATTCTGGCGCAGTTCGCGCTCCTGCTGCTCGCCTTTGGCG  >  NC_000913/4291367‑4291626

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap: ‑    Deleted base: ‑