Predicted mutation
evidence	seq id	position	mutation	annotation	gene	description
RA	1	92,936	G→A	T312T (ACC→ACT)	unknown ←	hypothetical protein

Read alignment evidence...
	seq id	position		ref	new	freq	score (cons/poly)	reads	annotation	genes	product
*	1	92,936	0	G	A	87.5%	12.9 / ‑5.6	8	T312T (ACC→ACT)	unknown	hypothetical protein
Reads supporting (aligned to +/- strand):  ref base G (0/1);  new base A (7/0);  total (7/1)
Fisher's exact test for biased strand distribution p-value = 1.25e-01
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 1.00e+00

TTCCGGCTGCAATCGGATAAACGGTGGTTAAAGTGCGGTCATAATTGCCCACGACCGCGCGTTTGAGCTTGATTTTGTTGGATTCAAGCGCACTAATCTCGACCATTTCTTTGTTTTTTCCTGTAATCAAAATGGCACGGCCACCGACGGCAAAATCATAGCCTGCGGTGTTAATAGCAAGCTCTGTGGCGCCCTGTTGCACATTTTGCAACAACTGGGCGCTGTCGGTAAAAATCGGCATCGACCACACGCGCGAGCCATAACCATAC  >  1/92914‑93182                       |                                                                                                                                                                                                                                                       ccgccgaacgcagcgggtAAACAGTGGTTAAAGTGCGCTCATAATTGCCCACGACCGCGCGCTTGAGCTTGATTTTACTCGGTTCAAGGGCGCTGATTTCGACCATTTCTTTGTTGCTTGCGGTCATCAAAATCGCGCGCCCGCCGATGGCAAAATCATAGCCTGCGGTGTTAATGGCAAGCTCTGTCGCCCCTTGTTGCACATTTTGCAACAACTGCGCGCTGTCGGTAAAAATc                                   >  1:839159/18‑236 (MQ=255)        ccgcagcGGATAAACGGTGTTTAAAGTGCGCTAATATTTCCCCACGCCCGCGCGTTTGAGTTTGTTTTTCCTCGGTTCAGGGGCGTTGTTTTCGACCTTTTTTTTGTTGCTTGCGGTCATAAAAACCGCGCGCCCGCCGATGGCAAAATCATAGCCTGCGGTGTTAATGGCAAGCTCTGTCGCCCCTTGTTGCACATTTTGCAACAACTGCGCGCTGTCGGTAAAAATCGGCATCGACCATACGCGCGAGc             <  1:653339/245‑1 (MQ=255)                ggtAAACAGTGGTTAAAGTGCGCTCATAATTGCCCACGACCGCGCGCTTGAGCTTGATTTTACTCGGTTCAAGGGCGCTGATTTCGACCATTTCTTTGTTGCTTGCGGTCATCAAAATCGCGCGCCCGCCGATGGCAAAATCATAGCCTGCGGTGTTAATGGCAAGCTCTGTCGCCCCTTGTTGCACATTTTGCAACAACTGCGCGCTGTCGGTAAAAATCGGCATCGACCATAcg                    >  1:187236/3‑236 (MQ=255)                ggtAAACAGTGGTTAAAGTGCGCTCATAATTGCCCACGACCGCGCGCTTGAGCTTGATTTTACTCGGTTCAAGGGCGCTGATTTCGACCATTTCTTTGTTGCTTGCGGTCATCAAAATCGCGCGCCCGCCGATGGCAAAATCATAGCCTGCGGTGTTAATGGCAAGCTCTGTCGCCCCTTGTTGCACATTTTGCAACAACTGCGCGCTGTCGGTAAAAATCGGCATCGACCATACGCGCGAGCCATAACCa     >  1:249910/3‑251 (MQ=255)                ggtAAACAGTGGTTAAAGTGCGCTCATAATTGCCCACGACCGCGCGCTTGAGCTTGATTTTACTCGGTTCAAGGGCGCTGATTTCGACCATTTCTTTGTTGCTTGCGGTCATCAAAATCGCGCGCCCGCCGATGGCAAAATCATAGCCTGCGGTGTTAATGGCAAGCTCTGTCGCCCCTTGTTGCACATTTTGCAACAACTGCGCGCTGTCGGTAAAAATCGGCATCGACCATACGCGCGAGCCATAACCa     >  1:543314/3‑251 (MQ=255)                ggtAAACAGTGGTTAAAGTGCGCTCATAATTGCCCACGACCGCGCGCTTGAGCTTGATTTTACTCGGTTCAAGGGCGCTGATTTCGACCATTTCTTTGTTGCTTGCGGTCATCAAAATCGCGCGCCCGCCGATGGCAAAATCATAGCCTGCGGTGTTAATGGCAAGCTCTGTCGCCCCTTGTTGCACATTTTGCAACAACTGCGCGCTGTCGGTAAAAATCGGCATCGACCATACGCGCGAGCCATAACCa     >  1:80681/3‑251 (MQ=255)                ggtAAACAGTGGTTAAAGTGCGCTCATAATTGCCCACGACCGCGCGCTTGAGCTTGATTTTACTCGGTTCAAGGGCGCTGATTTCGACCATTTCTTTGTTGCTTGCGGTCATCAAAATCGCGCGCCCGCCGATGGCAAAATCATAGCCTGCGGTGTTAATGGCAAGCTCTGTCGCCCCTTGTTGCACATTTTGCAACAACTGCGCGCTGTCGGTAAAAATCGGCATCGACCATACGCGCGAGCCATAACCa     >  1:886681/3‑251 (MQ=255)                   aaaCAGTGGTTAAAGTGCGCTCATAATTGCCCACGACCGCGCGCTTGAGCTTGATTTTACTCGGTTCAAGGGCGCTGATTTCGACCATTTCTTTGTTGCTTGCGGTCATCAAAATCGCGCGCCCGCCGATGGCAAAATCATAGCCTGCGGTGTTAATGGCAAGCTCTGTCGCCCCTTGTTGCACATTTTGCAACAACTGCGCGCTGTCGGTAAAAATCGGCATCGACCATACGCGCGAGCCATAACCATag  >  1:862101/1‑250 (MQ=255)                       |                                                                                                                                                                                                                                                       TTCCGGCTGCAATCGGATAAACGGTGGTTAAAGTGCGGTCATAATTGCCCACGACCGCGCGTTTGAGCTTGATTTTGTTGGATTCAAGCGCACTAATCTCGACCATTTCTTTGTTTTTTCCTGTAATCAAAATGGCACGGCCACCGACGGCAAAATCATAGCCTGCGGTGTTAATAGCAAGCTCTGTGGCGCCCTGTTGCACATTTTGCAACAACTGGGCGCTGTCGGTAAAAATCGGCATCGACCACACGCGCGAGCCATAACCATAC  >  1/92914‑93182

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 35 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap: ‑    Deleted base: ‑