Predicted mutation
evidence seq id position mutation annotation gene description
RA minE 326,795 Δ1 bp coding (272/963 nt) hemH → ferrochelatase

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*minE326,7930T.100.0% 143.0 / NA 33coding (270/963 nt)hemHferrochelatase
Reads supporting (aligned to +/- strand):  ref base T (0/0);  new base . (33/0);  total (33/0)

CAACAGCAGGCGCTGGCACAACGTTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCAC  >  minE/326770‑326842
                       |                                                 
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCAt     >  1:1503347/1‑69 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATc    >  1:2852772/1‑70 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:2270716/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:860915/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:2330113/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:2335284/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:2444919/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:289030/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:2968400/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:3028092/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:311522/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:3187978/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:3295465/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:532426/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:710987/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:776731/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:1375884/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:2234334/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:2226145/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:2147019/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:1932375/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:1906973/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:1883374/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:1877992/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:1818885/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:1796932/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:1765867/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:1763550/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:1692204/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:161651/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCa   >  1:159071/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCCCATCAc  >  1:435795/1‑71 (MQ=255)
cAACAGCAGGCGCTGGCACAACGTTACCGGAGATGCCCGTAGCGCTGGGAATGAACTACGGCTCGCCATCa   >  1:2223299/1‑71 (MQ=255)
                       |                                                 
CAACAGCAGGCGCTGGCACAACGTTTACCGGAGATGCCCGTAGCGCTGGGAATGAGCTACGGCTCGCCATCAC  >  minE/326770‑326842

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 21 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: