BRESEQ :: Evidence
Predicted mutation
evidence seq id position mutation freq annotation gene description
RA NC_012967 3,762,741 A→T 100% K662I (AAA→ATA)  spoT → bifunctional GTP diphosphokinase/guanosine‑3',5'‑bis pyrophosphate 3'‑pyrophosphohydrolase

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0129673,762,7410AT92.2% 23.7 / ‑5.6 11K662I (AAA→ATA) spoTbifunctional GTP diphosphokinase/guanosine‑3',5'‑bis pyrophosphate 3'‑pyrophosphohydrolase
Reads supporting (aligned to +/- strand):  ref base A (0/0);  major base T (7/3);  minor base G (0/1);  total (7/4)
Fisher's exact test for biased strand distribution p-value = 3.64e-01
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 1.00e+00
Rejected as polymorphism: E-value score below prediction cutoff.
Rejected as polymorphism: Variant not supported by required number of reads on each strand.

TCGAATATTCAAAGTTTGAATACGGAAGAGAAAGATGGTCGCGTCTACAGCGCCTTTATTCG > NC_012967/3762710‑3762771
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tCGAATATTCAAAGTTTGAATACGGAAGagatagat < 1:349403/36‑1 (MQ=38)
cGAATATTCAAAGTTTGAATACGGAAGAGATAGATg < 1:51621/36‑1 (MQ=38)
gAATATTCAAAGTTTGAATACGGAAGAGATAGATgg > 2:413795/1‑36 (MQ=38)
ttCAAAGTTTGAATACGGAACAGGTAGATGGTcggt > 2:215954/1‑34 (MQ=16)
cAAAGTTTGAATACGGAAGAGATAGATGGTCGCGTc < 2:528769/36‑1 (MQ=38)
ttGAATACGGAAGAGATAGATGGTCGCGTCTATAgc > 2:544213/1‑36 (MQ=25)
ttGAATACGGAAGAGATAGATGGTCGCGTCTACAgc < 1:138356/36‑1 (MQ=38)
tGAATACGGAAGAGATAGATGGTCGCGTCTACAgcg > 2:357014/1‑36 (MQ=38)
tGAATACGGAAGAGAGAGATGGTCGCGTCTACAgcg < 1:59172/36‑1 (MQ=39)
aTACGGAAGAGATAGATGGTCGCGTCTACAGTGCCt > 2:353043/1‑36 (MQ=25)
ggAAGAGATAGATGGTCGCGTCTACAGCGCCTTTAt > 2:560346/1‑36 (MQ=39)
agagATAGATGGTCGCGTCTACAGCGCCTTTATTCg > 2:72052/1‑36 (MQ=39)
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TCGAATATTCAAAGTTTGAATACGGAAGAGAAAGATGGTCGCGTCTACAGCGCCTTTATTCG > NC_012967/3762710‑3762771

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 8 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: