Predicted mutation
evidence seq id position mutation freq annotation gene description
RA NC_014034 2,526,995 A→G 100% P74P (CCT→CCC)  RCAP_rcc02356 ← hypothetical protein

Read alignment evidence...
  seq id position change freq score reads annotation genes product
*NC_0140342,526,9950A→G100.0% 11.5 3P74P (CCT→CCC) RCAP_rcc02356hypothetical protein
Reads supporting (aligned to +/- strand):  new base (0/3):  ref base (0/0):  total (0/3)

GTTCGGGTTTCGCGGGCGGCTCGGTCGCAGGCGCGGCAACGGCGGGCGGCTCGGCCCGGGGCGCGGGCGCCGAAGCCGCGGGCCGTTCCCGGGGCGCAGGCGGTGCGGCAGGCGGGGGCT  >  NC_014034/2526898‑2527017
                                                                                                 |                      
gttggggttTCGCGGGCGGCTCGGTCGCAGGCGCGGCAACGGCGGGCGGCTCGGCCCGGGGCGCGGGCGCCGAAGCCGCGGGCCGTTCCCGGGGCGCGGGc                     <  2:577084/101‑1 (MQ=255)
    gggtgccgggggcggCGCGGGCGCAGGCGCGGAAACGGCGGGCGGCTGGGCCGGGGGCGGGGGCGCCGAAGCCGCGGGCCGTTCCCGGGGCGCGGGCGGTg                 <  1:3461144/92‑1 (MQ=255)
                   ccggggggggggCGCGGCAGGGGGGGGCGCCCCGGCCGGGGGCGGGGGCCCCGAAGCCGGGGGCCGTTCCCGGGGCGCGGGCGGTGCGGCGGGCGGGGGCt  <  1:1057171/91‑1 (MQ=255)
                                                                                                 |                      
GTTCGGGTTTCGCGGGCGGCTCGGTCGCAGGCGCGGCAACGGCGGGCGGCTCGGCCCGGGGCGCGGGCGCCGAAGCCGCGGGCCGTTCCCGGGGCGCAGGCGGTGCGGCAGGCGGGGGCT  >  NC_014034/2526898‑2527017

Base quality scores:  ATCG  < 3 ≤  ATCG  < 20 ≤  ATCG  < 21 ≤  ATCG  < 33 ≤  ATCG  < 41 ≤  ATCG