Predicted mutation
evidence seq id position mutation annotation gene description
RA NC_007793 2,811,673 G→A S2170S (TCC→TCT)  SAUSA300_RS14395 ← serine‑rich adhesin for platelets

Read alignment evidence...
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_0077932,811,6730GA100.0% 23.8 / NA 11S2170S (TCC→TCT) SAUSA300_RS14395serine‑rich adhesin for platelets
Reads supporting (aligned to +/- strand):  ref base G (0/0);  new base A (8/3);  total (8/3)

TGCTCGTTGTTGCTTCACTTGATAAGCGAGATGTGCTCGTGCTGTGAGTATGATGCATACTCATTGAGTCTGACGGATGCATTGAGTTAGATTCGGATGTACTTGTTGAGCCGGACATACTTGTTGATGTTGAGTCAGAAATGCTTTGTGAACCAGACATAGATGTACTCAGTGATTCGGATGTGCTTGTC  >  NC_007793/2811579‑2811769
                                                                                              |                                                                                                
tGCTCGTTGTTGCTTCACTTGATAAGCGCGATGTGCTCGTGCTGTGAGTATGATGCATACTCATTGAGTCTGACGGATGCATTGAGTTAGATTCAGATGt                                                                                             >  1:2868734/1‑100 (MQ=255)
                                  gCTCGTGCTGTGAGTATGATGCATACTCATTGAGTCTGACGGATGCATTGAGTTAGATTCAGATGTACTTGTTGAGCCGGACATACTTGTTGATGTTGAg                                                           >  1:1357988/1‑100 (MQ=255)
                                   cTCGTGCTGTGAGTATGATGCATACTCATTGAGTCTGACGGATGCATTGAGTTAGATTCAGATGTACTTGTTGAGCCGGACATACTTGTTGATGTTGAGt                                                          >  1:82804/1‑100 (MQ=255)
                                    tCGTGCTGTGAGTATGATGCATACTCATTGAGTCTGACGGATGCATTGAGTTAGATTCAGATGTACTTGTTGAGCCGGACATACTTGTTGATGTTGAGTc                                                         <  1:1784946/100‑1 (MQ=255)
                                           gtgAGTATGATGCATACTCATTGAGTCTGACGGATGCATTGAGTTAGATTCAGATGTACTTGTTGAGCCGGACATACTTGTTGATGTTGAGTCAGAAATg                                                  >  1:3659667/1‑100 (MQ=255)
                                                            tCATTGAGTCTGACGGATGCATTGAGTTAGATTCAGATGTACTTGTTGAGCCGGACATACTTGTTGATGTTGAGTCAGAAATGCTTTGTGAACCAGACAt                                 <  1:4453324/100‑1 (MQ=255)
                                                                     cTGACGGGTGCATTGAGTTAGATTCAGATGTACTTGTTGAGCCGGACATACTTGTTGATGTTGAGTCAGAAATGCTTTGTGAACCAGACATAGATGTACt                        >  1:6137658/1‑100 (MQ=255)
                                                                     cTGACGGATGCATTGAGTTAGATTCAGATGTACTTGTTGAGCCGGACATACTTGTTGATGTTGAGTCAGAAATGCTTTGTGAACCAGACATAGATGTACt                        >  1:1866000/1‑100 (MQ=255)
                                                                       gACGGATGCATTGAGTTAGATTCAGATGTACTTGTTGAGCCGGACATACTTGTTGATGTTGAGTCAGAAATGCTTTGTGAACCAGACATAGATGTACTCa                      >  1:6617455/1‑100 (MQ=255)
                                                                              gCATTGAGTTAGATTCAGATGTACTTGTTGAGCCGGACATACTTGTTGATGTTGAGTCAGAAATGCTTTGTGAACCAGACATAGATGTACTCAGTGATTc               >  1:1410102/1‑100 (MQ=255)
                                                                                           ttCAGATGTACTTGTTGAGCCGGACATACTTGTTGATGTTGAGTCAGAAATGCTATATGAACCAGACATAGATGTACTCAGTGATTTGGATGTGCTTGTc  <  1:3759112/100‑1 (MQ=255)
                                                                                              |                                                                                                
TGCTCGTTGTTGCTTCACTTGATAAGCGAGATGTGCTCGTGCTGTGAGTATGATGCATACTCATTGAGTCTGACGGATGCATTGAGTTAGATTCGGATGTACTTGTTGAGCCGGACATACTTGTTGATGTTGAGTCAGAAATGCTTTGTGAACCAGACATAGATGTACTCAGTGATTCGGATGTGCTTGTC  >  NC_007793/2811579‑2811769

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 17 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap: ‑    Deleted base: ‑