Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_000913 1,730,552 C→T A489V (GCC→GTC)  lhr → ATP‑dependent helicase Lhr

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0009131,730,5520CT90.9% 18.0 / NA 11A489V (GCC→GTC) lhrATP‑dependent helicase Lhr
Reads supporting (aligned to +/- strand):  ref base C (0/0);  major base T (3/7);  minor base G (0/1);  total (3/8)
Fisher's exact test for biased strand distribution p-value = 1.00e+00
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.82e-01

GGGTTACAACGCATTGGTCGCGCCGGACATCAGGTTGGCGGTGTATCTAAAGGGCTGTTTTTCCCCCGTACCCGGCGTGATTTAGTCGATTCCGCAGTCATTGTAGAGTGTATGTTCGCAGGCAGGCTGGAAAACCTGACACCACCGCATAATCCTCTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGATGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGCCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTTCCGGGCGCTATCCCTCTGGCGATTTTTCTGCTTTTCGCCCCAAACTGGTCTGGAACAGGGAGACCGGGATATTGACCGCCCGACCTGGCGCTCAATTGTTGGCGGTTACCAGCGGCGGCACCATTCCGGATC  >  NC_000913/1730311‑1730740
                                                                                                                                                                                                                                                 |                                                                                                                                                                                            
gggTTACAACGCATTGGTCGCGCCGGACATCAGGTTGGCGGTGTATCTAAAGGGCTGTTTTTCCCCCGTACCCGGCGTGATTTAGTCGATTCCGCAGTCATTGTAGAGTGTATGTTCGCAGGCAGGCTGGAAAACCTGACACCACCGCATAATCCTCTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGAGGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGTCGCACCGTg                                                                                                                                                                                     <  1:104578/251‑1 (MQ=255)
                      ccGGACATCAGGTTGGCGGTGTATCTAAAGGGCTGTTTTTCCCCCGTACCCGGCGTGATTTAGTCGATTCCGCAGTCATTGTAGAGTGTATGTTCGCAGGCAGGCTGGAAAACCTGACACCACCGCATAATCCTCTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGATGCATTACAGGAAGACGAATGGTACTCCCGCGTACGCCGTGTCGCACCGTGGAAAGATc                                                                                                                                                                             >  1:60941/1‑237 (MQ=255)
                                                aaaGGGCTGTTTTTCCCCCGTACCCGGCGTGATTTAGTCGATTCCGCAGTCATTGTAGAGTGTATGTTCGCAGGCAGGCTGGAAAACCTGACACCACCACATAATCCTCTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGTATGCATTACAGGGAGACGGATGGTACTCCCGCGTACGCCGTGGCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGc                                                                                                                                         <  1:221781/247‑1 (MQ=255)
                                                    ggCTGTTTTTCCCCCGTACCCGGCGTGATTTAGTCGATTCCCCCGTCATTGTAGAGTGTATGTTCCCAGGCACGCTGGAAAAACTGACAACACCGCCTAATCCTCTCGAAGTCCTTGCGCGGCCAACCGTTGCCGCCGCGGAGATGGATGCATTACAGGTAGACGGATGGGACTCCCGCGTAAGCCGTGTCGCCCCGTGGAAAGATCTGCCACGCCGTGTTTTTGACGCCCCGCTGGATATGTTTTCCggg                                                                                                                                 >  1:98415/1‑251 (MQ=255)
                                                           tttCCCCCGTACCCGGCGTGATTTAGTCGATTCCGCAGTCATTGTAGAGTGTATGTTCGCAGGCAGGCTGGAAAACCTGACACCACCGCATAATCCTCTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGATGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGTCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGc                                                                                                                                         <  1:108677/236‑1 (MQ=255)
                                                                                    gTCGATTCCGCAGTCATTGTAGAGTGTATGTTCGCAGGCAGGCTGGAAAACCTGACACCACCGCATAATCCTCTCTACGTCCTGGCGCAGCAAACCGGTGCCGCCGCGGCGAGGGGTGCAGGACAGGTAGACTAATGGTACTCCCGCGTACGCCGTGTCGCACCGTGGaa                                                                                                                                                                                  <  1:202812/170‑1 (MQ=255)
                                                                                                                           aggcTGGAAAACCTGACACCACCGCATAATCCTCTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGATGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGTCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTTCCGGGCGCTATCCCTCTGGCGATTTTTCTGCTTTTCGCCCCAAACTGGTCTGGAACAGGGAGACCGGGATATTGAc                                                          <  1:62394/251‑1 (MQ=255)
                                                                                                                                ggAAAACCTGACACCACCGCATAATCCTCTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGATGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGTCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTTCCGGGCGCTATCCCTCTGGCGATTTTTCTGCTTTTCGCCCCAAACTGGTCTGGAACAGGGAGACCGGGATATTGACCGccc                                                     >  1:115433/1‑251 (MQ=255)
                                                                                                                                ggAAAACCTGACACCACCGCATAAGCCTCGCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGAAGCATTACAGGTAGACGAATGGTACTCCCGCGTACGGCGTGTCGCACCGGGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTTCCGGGCGCTATCCCTCTGGCGATTTTTCTGCTTTTCGCCCCAAACTGGTCTGGAACAGGGAGACCGGGATATTGACCga                                                       <  1:118731/249‑2 (MQ=255)
                                                                                                                                         gACACCACCGCATAATCCTTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGATGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGTCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTGCCGGGCGCTATCCCACTGGCGATTTTTCGGCTTTTCGCCCCAAACTGGTCTTGAACAGGGAGACCGGGATATTGACCGCCCGACCTGgcn                                            <  1:40651/250‑2 (MQ=255)
                                                                                                                                                                                   cGTTGCCGCCGCGGCGATGGATGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGTCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTTCCGGGCGCTATCCCTCTGGCGATTTTTCTGCTTTTCGCCCCAAACTGGTCTGGAACAGGGAGACCGGGATATTGACCGCCCGACCTGGCGCTCAATTGTTGGCGGTTACCAGCGGCGGCACCATTCCGGAtn  <  1:135010/251‑2 (MQ=255)
                                                                                                                                                                                                                                                 |                                                                                                                                                                                            
GGGTTACAACGCATTGGTCGCGCCGGACATCAGGTTGGCGGTGTATCTAAAGGGCTGTTTTTCCCCCGTACCCGGCGTGATTTAGTCGATTCCGCAGTCATTGTAGAGTGTATGTTCGCAGGCAGGCTGGAAAACCTGACACCACCGCATAATCCTCTCGACGTCCTTGCGCAGCAAACCGTTGCCGCCGCGGCGATGGATGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGCCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTTCCGGGCGCTATCCCTCTGGCGATTTTTCTGCTTTTCGCCCCAAACTGGTCTGGAACAGGGAGACCGGGATATTGACCGCCCGACCTGGCGCTCAATTGTTGGCGGTTACCAGCGGCGGCACCATTCCGGATC  >  NC_000913/1730311‑1730740

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: