Predicted mutation
evidence seq id position mutation annotation gene description
RA REL606 2,031,537 A→T S421T (TCC→ACC)  manB ← Phosphomannomutase

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*REL6062,031,5370AT94.4% 46.5 / NA 18S421T (TCC→ACC) manBPhosphomannomutase
Reads supporting (aligned to +/- strand):  ref base A (0/0);  major base T (8/9);  minor base C (0/1);  total (8/10)
Fisher's exact test for biased strand distribution p-value = 1.00e+00
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 1.00e+00

TGTCTTTTCTTCCATCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTGTTGGAGGAGCGCAGGTTAAAGCGCCAGTCGGCA  >  REL606/2031463‑2031562
                                                                          |                         
tGTCTTTTCTTCCATCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGCATTGgaggag                          >  2:1056907/1‑76 (MQ=255)
   cTTTTCTTCCATCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTgcgc                       >  2:510068/1‑76 (MQ=255)
   cTTTTCTTCCATCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTgcgc                       >  2:455603/1‑76 (MQ=255)
   cTTTTCTTCCATCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTgcgc                       >  2:231553/1‑76 (MQ=255)
   cTTTTCTTCCATCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTgcgc                       >  1:439277/1‑76 (MQ=255)
   cTTTTCTTCCATCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTgcgc                       <  2:1105292/76‑1 (MQ=255)
     tttCTTCCATCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTGCGCAg                     >  2:1530243/1‑76 (MQ=255)
     tttCTCCCATCAGCGGTACACCCCCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTGCGCAg                     <  1:950435/76‑1 (MQ=14)
      ttcttcCATCATCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTGCGCAgg                    >  1:43378/1‑76 (MQ=11)
      ttcttcCATCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTGCGCAgg                    >  1:655258/1‑76 (MQ=255)
        cttcCATCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTGCGCAGGtt                  <  1:1570369/76‑1 (MQ=255)
        cttcCATCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTGCGCAGGtt                  >  2:1584203/1‑76 (MQ=255)
        cttcCATCAGCGGTACATCACCGCGCGATTCCACACTCAACCGCACCACCGGTTCGGTATTGGAGGTGCGCAGGtt                  >  1:359395/1‑76 (MQ=11)
          tcCATCAGCGGTACATCCCCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTGCGCAGGTTaa                <  1:1123992/76‑1 (MQ=11)
          tcCATCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTGCGCAGGTTaa                <  2:845780/76‑1 (MQ=255)
          tcCATCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTGCGCAGGTTaa                <  1:636921/76‑1 (MQ=255)
             aTCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTGCGCATNTTAAAgc             <  2:1433434/76‑1 (MQ=11)
             aTCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTGCGCAGGTTAAAgc             <  1:348727/76‑1 (MQ=255)
              tCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGCGCGCAGGTTAAAgcg            <  1:156940/76‑1 (MQ=255)
                  cGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTATTGGAGGTGCGCAGGTTAAAGCGCCAg        <  1:1567148/76‑1 (MQ=255)
                        aTCACCGCGCGATTCCACATTCCACCGGCCCGCCGGTACGGTGTTGTAGGAGCGCATGTTAATGCGTCAGTCGGCa  <  1:1711268/76‑1 (MQ=17)
                                                                          |                         
TGTCTTTTCTTCCATCAGCGGTACATCACCGCGCGATTCCACATTCAACCGCACCACCGGTTCGGTGTTGGAGGAGCGCAGGTTAAAGCGCCAGTCGGCA  >  REL606/2031463‑2031562

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 24 ≤ ATCG/ATCG < 31 ≤ ATCG/ATCG < 35 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: