Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_007793 613,318 T→A S724S (TCT→TCA)  SAUSA300_RS02915 → serine‑aspartate repeat‑containing protein C

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_007793613,3180TA88.9% 15.1 / ‑4.2 9S724S (TCT→TCA) SAUSA300_RS02915serine‑aspartate repeat‑containing protein C
Reads supporting (aligned to +/- strand):  ref base T (0/0);  major base A (7/1);  minor base G (1/0);  total (8/1)
Fisher's exact test for biased strand distribution p-value = 1.00e+00
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.73e-01

GTAACAATTACGGATCATGATGATTTCACACTTGATAATGGCTACTACGAAGAAGAAACATCAGATAGCGACTCAGATTCTGACAGCGATTCAGACTCAGATAGCGACTCAGATTCAGATAGCGACTCAGATTCAGACAGCGATTCAGACAGCGACTCAGACTCAGATAGCGA  >  NC_007793/613238‑613410
                                                                                |                                                                                            
gTAACAATTACGGATCATGATGATTTCACACTTGATAATGGCTACTACGAAGAAGAAACATCAGATAGCGACTCAGATTCAGACAGCGATTCAGACtcag                                                                           >  1:2724978/1‑100 (MQ=255)
                atgatgATTTCACACTTGATAATGGCTACTACGAAGAAGAAACATCAGATAGCGACTCAGATTCAGACAGCGATTCAGACtcagatagcgactcagattc                                                           <  1:6614854/100‑1 (MQ=255)
                          cacaCTTGATAATGGCTACTACGAAGAAGAAACATCAGATAGCGACTCAGATTCAGACAGCGATTCAGACtcagatagcgactcagattcagatagcgac                                                 >  1:3727239/1‑100 (MQ=255)
                                  ctAATGGCTACTACGAAGAAGAAACATCAGATAGCGACTCAGATTCAGACAGCGATTCAGACTCagatagcgactcagattcagatagcgactcagattc                                         >  1:5438779/2‑100 (MQ=255)
                                       ggCTACTACGAAGAAGAAACATCAGATAGCGACTCAGATTCAGACAGCGATTCAGACTCAGATAGCGACTCAGATTCAGATAGCGACTCAgattcagaca                                    >  1:5487822/1‑100 (MQ=255)
                                                        cgacgcAGATAGCGATTCTGATGCGGACAGCGATTCAGACGCAGATAGCGATTCAGATTCAGATAGCGATTCTgatgcggacagcgattcagccacagat                   >  1:1500651/6‑95 (MQ=0)
                                                             cAGATAGCGACTCAGATTCAGACAGCGATTCAGACTCAGATAGCGACTCAGATTCAGATAGCGACTCAGATTCAGACAGCGATTCAGACAGCgactcaga              >  1:1629896/1‑100 (MQ=255)
                                                             cAGACAGCGATTCAGACGCAGATAGCGACTCAGACGCAGATAGCGACTCTGATGCGGACAGCGACTCAgattcagacagcgattcagaccgcagatcgga              >  1:5739114/1‑92 (MQ=11)
                                                                         cAGATTCAGACAGCGATTCAGACTCAGATAGCGACTCAGATTCAGATAGCGACTCAGATTCAGACAGCGATTCAGACAGCGACTCAGACTCAGATAGCga  >  1:2081049/1‑100 (MQ=255)
                                                                                |                                                                                            
GTAACAATTACGGATCATGATGATTTCACACTTGATAATGGCTACTACGAAGAAGAAACATCAGATAGCGACTCAGATTCTGACAGCGATTCAGACTCAGATAGCGACTCAGATTCAGATAGCGACTCAGATTCAGACAGCGATTCAGACAGCGACTCAGACTCAGATAGCGA  >  NC_007793/613238‑613410

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 16 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap: ‑    Deleted base: ‑