Predicted mutation
evidence	seq id	position	mutation	annotation	gene	description
RA	NC_000913	387,234	G→T	M88I (ATG→ATT)	tauC →	taurine ABC transporter membrane subunit

Read alignment evidence...
	seq id	position		ref	new	freq	score (cons/poly)	reads	annotation	genes	product
*	NC_000913	387,234	0	G	T	100.0%	24.9 / NA	10	M88I (ATG→ATT)	tauC	taurine ABC transporter membrane subunit
Reads supporting (aligned to +/- strand):  ref base G (0/0);  new base T (4/6);  total (4/6)

GCCGCAACAGGTACTGGAAAAACTACTCACCATTGCCGGACCGCAAGGCTTTATGGACGCCACGCTGTGGCAGCATCTGGCAGCCAGTCTGACGCGCATTATGCTGGCGCTATTTGCAGCGGTGTTGTTCGGTATTCCGGTCGGGATCGCGATGGGACTTAGCCCTACGGTACGCGGCATTCTGGATCCGATAATCGAGCTTTATCGTCCGGTGCCGCCGCTGGCTTATTTGCCGCTGATGGTGATCTGGTTTGGTATTGGTGAAACCTCGAAGATCTTACTGATCTATTTAGCGATTTTTGCACCGGTGGCGATGTCGGCGCTGGCGGGGGTGAAAAGCGTGCAGC  >  NC_000913/387132‑387478                                                                                                       |                                                                                                                                                                                                                                                     gccgcAACAGGTACTGGAAAAACTACTCACCATTGCCGGACCGCAAGGCTTTATGGACGCCACGCTGTGGCAGCATCTGGCAGCCAGTCTGACGCGCATTATTCTGGCGCTATTTg                                                                                                                                                                                                                                         <  1:15903/116‑1 (MQ=255)   ngcAACAGGTACTGGCAAAACTACTCACCATTGCCGGCCCGCAAGGCTTTATGCACGCCACGCTGTGGCCGCATCTGGCAGCCAGTCTGACGCGCCTTATTCTGGCGCTATTTGCAGCGGTGTTGTTCGGTATTCCGGTCGGGATCGCGATGGGACTTAGc                                                                                                                                                                                          >  1:43848/2‑161 (MQ=255)                     aaCTACTCACAATGGCCGGACCGCAAGGCTTTATGGACGCCACGCTGTGGCAGCATCTGGCAGCCAGTCTGACGCGCATTATTCTGGCGCTATTTGCAGCGGTGTTGTTCGGTATTCCGGTCGGGATCGCGATGGGACTTAGCCCTCCGGTTCGCGGCATTCTGGATCCGATAATCGAGCTGTATCGGCCGGTGCCGCCGCTGGCTTATTTGCCGCTGATGGTGATCTGGTTCGGTATTGGTGAAACCTcn                                                                              <  1:26734/251‑2 (MQ=255)                                    ccGGACCGCAAGGCTTTATGGACGCCACGCTGTGGCAGCATCTGGCAGCCAGTCTGACGCGCATTATTCTGGCGCTATTTGCAGCGGTGTTGTTCGGTATTCCGGTCGGGATCGCGATGGGACTTAGCCCTACGGTACGCGGCATTCTGGATCCGATAATCGAGCTTTATCGTCCGGTGCCGCCGCTGGCTTATTTGCCGCTGATGGTGATCTGGTTTGGTATTGGTGAAACCTCGAAGATCTTACTGATc                                                               <  1:167121/251‑1 (MQ=255)                                         ccGCAAGGCTTTATGGACGCGACGCTGTGGCAGCATCTGGAAGCCAGTCTGACGCGCATTCTTCTGGCGCTATTTGAAGCGGTGTTGTTCGGTATTCCGGTCGGGATCGCGATGGGACTTAGCCCTACGGTACGCGGCATTCTGGATCCGATAATCGAACTTTATCGTCCGGTgccg                                                                                                                                    >  1:111675/1‑177 (MQ=255)                                           gCAAGGCTTTATGTACGCCACGCTGTGGCAGCATCTGGCAGCCAGTCTGACGCGCATTATTCTGGCGCTATTTGCAGCGGTGTTGTTCGGTATTCCGGTCGGGATcgcgct                                                                                                                                                                                                    <  1:210735/111‑3 (MQ=255)                                                    tATGGACGCCACGCTGTGGCAGCATCTGGCAGCAAGTCTGACGCGAATGATTCTGCCGTTATTGGCAGCG‑TGTTGTTCGGTATTCCGGTCGGGATCGCGATGGGACTTAGCCCTACGGTACGCGGCATTCTGGATCCGATAATCGAGCTTTATCGTCCGGTGCCGCCGCTGGCTTATTTGCCGCTGATGGTGATCTGGTTTGGTATTGGTGAAACCTCGAAGATCTGACTGATCTATTTAGCGATTTTTg                                               <  1:17906/250‑1 (MQ=255)                                                                               ggCAGCCAGTCTGACGCGCATTATTCTGGCGCTATTTGCAGCGGTGTTGTTCGGTATTCCGGTCGGGATCGCGATGGGACTTAGCCCTACGGTACGCGGCATTCTGGATCCGATAATCGAGCTTTATCGTCCGGTGCCGCCGCTGGCTTATTTGCCGCTGATGGTGATCTGGTTTGGTATTGGTGAAACCTCGAAGATCTTACTGATCTATTTAGCGATTTTTGCACCGGTGGCGATGTCGGCGCTGGCgg                    <  1:164956/251‑1 (MQ=255)                                                                                   gCCAGTCTGACGCGCATTATTCTGGCGCTATTTGCAGCGGTGTTGTTCGGTATTCCGGTCGGGATCGCGATGGGACTTAGCCCTACGGTACGCGGCATTCTGGATCCGATAATCGAGCTTTATCGTCCGGTGCCGCCGCTGGCTTATTTGCCGCTGATGGTGATCTGGTTTGGTATTGGTGAAACCTCGAAGATCTTACTGATCTATTTAGc                                                       >  1:5843/1‑212 (MQ=255)                                                                                                 cATTATTCTGGCGCGATTTGCAGCGGTGTTGTTCGGTATTCCGGTCGGGATCGCAATGGGACTTAGCCCTACGGTACGCGACATTCTGTTACAGATAATCTAGCTTTATCGTCCGGTGCCGCCGCGGGATTATTTGCCGCTGATGGTGATCTGGTTTGGTATTGGTGAAACCTCGAAGCTCTTACTGATATCTTTAGCGATTTTTGCACCGGTGGCGATGGCGGCGCTGGCTGGGGTGAAAcgcggggagc  >  1:198694/1‑245 (MQ=255)                                                                                                       |                                                                                                                                                                                                                                                     GCCGCAACAGGTACTGGAAAAACTACTCACCATTGCCGGACCGCAAGGCTTTATGGACGCCACGCTGTGGCAGCATCTGGCAGCCAGTCTGACGCGCATTATGCTGGCGCTATTTGCAGCGGTGTTGTTCGGTATTCCGGTCGGGATCGCGATGGGACTTAGCCCTACGGTACGCGGCATTCTGGATCCGATAATCGAGCTTTATCGTCCGGTGCCGCCGCTGGCTTATTTGCCGCTGATGGTGATCTGGTTTGGTATTGGTGAAACCTCGAAGATCTTACTGATCTATTTAGCGATTTTTGCACCGGTGGCGATGTCGGCGCTGGCGGGGGTGAAAAGCGTGCAGC  >  NC_000913/387132‑387478

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: ‑