Predicted mutation
evidence	seq id	position	mutation	annotation	gene	description
RA	NC_007793	2,000,306	T→G	noncoding (392/2926 nt)	SAUSA300_RS10040 ←	23S ribosomal RNA

Read alignment evidence...
	seq id	position		ref	new	freq	score (cons/poly)	reads	annotation	genes	product
*	NC_007793	2,000,306	0	T	G	100.0%	14.4 / NA	13	noncoding (392/2926 nt)	SAUSA300_RS10040	23S ribosomal RNA
Reads supporting (aligned to +/- strand):  ref base T (0/0);  new base G (13/0);  total (13/0)

ATTTAGCCTTAGGAGATGGTCCTCCCAGATTCCGACGGAATTTCACGTGTTCCGTCGTACTCAGGATCCACTCAAGAGAGACAACATTTTCGACTACAGGATTATTACCTTCTTTGATTCATCTTTCCAGATGATTCGTCTAATGTCG  >  NC_007793/2000220‑2000367                                                                                       |                                                              aTTTAGCCTTGGGAGATGGTCCTCCCGGATTCCGACGGAATTTCACGTGTTCCGCCGTACTCAGGACCCACTCAGGAGAGAACGAAGTTTTGACTACAgg                                                  >  1:3966395/1‑100 (MQ=11)   ttAGCCTTGGGAGATGGTCCTCCCGGATTCCGACGGAATTTCACGTGTTCCGCCGTACTCAGGATCCACTCAGGAGAGAACGAAGTTTTGACTACAgggc                                                >  1:1188375/1‑98 (MQ=11)   ttAGCCTTGGGAGATGGTCCTCCCGGATTCCGACGGAATTTCACGTGTTCCGCCGTACTCAGGATCCACTCAGGAGAGAACGAAGTTTTGACTACAgggc                                                >  1:2052484/1‑98 (MQ=11)   ttAGCCTTGGGAGATGGTCCTCCCGGATTCCGACGGAATTTCACGTGTTCCGCCGTACTCAGGATCCACTCAGGAGAGAACGAAGTTTTGACTACAgggc                                                >  1:5207377/1‑98 (MQ=11)    tAGCCTTGGGAGATGGTCCTCCCGGATTCCGACGGAATTTCACGTGTTCCGCCGTACTCAGGATCCACTCAGGAGAGAACGAAGTTTTGACTACAgggct                                               >  1:1831766/1‑97 (MQ=11)    tAGCCTTGGGAGATGGTCCTCCCGGATTCCGACGGAATTTCACGTGTTCCGCCGTACTCAGGATCCACTCAGGAGAGAACGAAGTTTTGACTACAgggct                                               >  1:1987959/1‑97 (MQ=11)    tAGCCTTGGGAGATGGTCCTCCCGGATTCCGACGGAATTTCACGTGTTCCGCCGTACTCAGGATCCACTCAGGAGAGAACGAAGTTTTGACTACAgggct                                               >  1:587029/1‑97 (MQ=11)     cgCCTTGGGAGATGGTCCTCCCGGATTCCGACGGAATTTCACGTGTTCCGCCGTACTCAGGATCCACTCAGGAGAGAACGAAGTTTTGACTACAgggctg                                              >  1:4134688/2‑96 (MQ=11)     aGCCTTGGGAGATGGTCCTCCCGGATTCCGACGGAATTTCACGTGTTCCGCCGTACTCAGGATCCACTCAGGAGAGAACGAAGTTTTGACTACAgggctg                                              >  1:2431906/1‑96 (MQ=11)     aGCCTTGGGAGATGGTCCTCCCGGATTCCGACGGAATTTCACGTGTTCCGCCGTACTCAGGATCCACTCAGGAGAGAACGAAGTTTTGACTACAgggctg                                              >  1:4082830/1‑96 (MQ=11)     aGCCTTGGGAGATGGTCCTCCCGGATTCCGACGGAATTTCACGTGTTCCGCCGTACTCAGGATCCACTCAGGAGAGAACGAAGTTTTGACTACAgggcag                                              >  1:859698/1‑96 (MQ=11)     aGCCTTGGGAGATGGGCCTCCCGGATTCCGACGGAATTTCACGTGTTCCGCCGTACTCAGGATCCACTCAGGAGAGAACGAAGTTTTGACTACAgggctg                                              >  1:1710462/1‑96 (MQ=11)                                                 gtTCCGCCGTACTCAGGATCCACTCAGGAGAGAACGAAGTTTTGACTACAGGGCTGTTACCTTCTTTGATTCATCTTTCCAGATGATTCGTCTAATgtcg  >  1:4939747/1‑100 (MQ=2)                                                                                       |                                                              ATTTAGCCTTAGGAGATGGTCCTCCCAGATTCCGACGGAATTTCACGTGTTCCGTCGTACTCAGGATCCACTCAAGAGAGACAACATTTTCGACTACAGGATTATTACCTTCTTTGATTCATCTTTCCAGATGATTCGTCTAATGTCG  >  NC_007793/2000220‑2000367

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 23 ≤ ATCG/ATCG < 29 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap: ‑    Deleted base: ‑