Predicted mutation
evidence seq id position mutation freq annotation gene description
RA minE 2,398,903 T→C 100% E576E (GAA→GAG uvrD ← DNA‑dependent ATPase I and helicase II

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*minE2,398,9030TC100.0% 13.5 / NA 5E576E (GAA→GAGuvrDDNA‑dependent ATPase I and helicase II
Reads supporting (aligned to +/- strand):  ref base T (0/0);  new base C (5/0);  total (5/0)
Rejected as polymorphism: Frequency below/above cutoff threshold.
Rejected as polymorphism: Variant not supported by required number of reads on each strand.

TGGCTTGGGAACATGCCCTCTTCCATACCAACGATAAA  >  minE/2398883‑2398920
                    |                 
tGGCTTGGGAACATGCCCTCCTCCATACCAACGATaaa  >  1:225632/1‑38 (MQ=255)
tGGCTTGGGAACATGCCCTCCTCCATACCAACGATaaa  >  1:279292/1‑38 (MQ=255)
tGGCTTGGGAACATGCCCTCCTCCATACCAACGATaaa  >  1:335220/1‑38 (MQ=255)
tGGCTTGGGAACATGCCCTCCTCCATACCAACGATaaa  >  1:368397/1‑38 (MQ=255)
tGGCTTGGGAACATGCCCTCCTCCATACCAACGATaaa  >  1:439037/1‑38 (MQ=255)
                    |                 
TGGCTTGGGAACATGCCCTCTTCCATACCAACGATAAA  >  minE/2398883‑2398920

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: