Predicted mutation
evidence seq id position mutation freq annotation gene description
RA NC_014034 2,527,007 A→G 100% P70P (CCT→CCC)  RCAP_rcc02356 ← hypothetical protein

Read alignment evidence...
  seq id position change freq score reads annotation genes product
*NC_0140342,527,0070A→G100.0% 11.4 3P70P (CCT→CCC) RCAP_rcc02356hypothetical protein
Reads supporting (aligned to +/- strand):  new base (3/0):  ref base (0/0):  total (3/0)

CGGGGCGCAGGCGGTGCGGCAGGCGGGGGCTCGGCCGCGGGGCGGGCGACGCCCGCGGCTTCGGGCAGCGCCACGGCCTGCGCCGGGGCGGGATCG.GCGGGCGCGGTCCGGGGTG  >  NC_014034/2526987‑2527101
                    |                                                                                               
cGGGGCGCGGGCGGTGCGGCGGTCGGGGGCTCGGCCGCGGGGCGGGCGACGCCCGCGGCTTCGGGCAGCGCCACGGCCTGCGCCGGGGCGGGGTCg.gcggg                >  1:4022614/1‑101 (MQ=255)
  gggCGCGGGCGGTGCGGCGGGCGGGGGCCCGGCCGCGGGGGGGGGGGCGCCCGCGGCGTCGGGCAGCGCCACGGCCCTCGCCGGGGCGGGGTCg.gcggggg              >  2:3975400/1‑99 (MQ=255)
               gCGGCGGGCGGGGGCTCGGCCGCGGGGGGGGGGACGCCCGCGGGCTCGGGCAACGCCCCGGGCTGAGCCCGGGGGGGGTCGCGCGGGggcgcggggggggg  >  2:1517433/1‑91 (MQ=255)
                    |                                                                                               
CGGGGCGCAGGCGGTGCGGCAGGCGGGGGCTCGGCCGCGGGGCGGGCGACGCCCGCGGCTTCGGGCAGCGCCACGGCCTGCGCCGGGGCGGGATCG.GCGGGCGCGGTCCGGGGTG  >  NC_014034/2526987‑2527101

Base quality scores:  ATCG  < 3 ≤  ATCG  < 15 ≤  ATCG  < 18 ≤  ATCG  < 23 ≤  ATCG  < 37 ≤  ATCG