num_system |
Designates the numbering system (e.g., Kabat, IMGT) used to number codon positions |
identity |
Percent of nucleotide sequence identity (e.g., 90 %) between aligned portions of a read sequence and a germline gene segment sequence |
score |
Alignment score, as defined by the aligner software |
insertions |
Number of nucleotide insertions in the read sequence relative to the germline sequence |
deletions |
Number of nucleotide deletions from the read sequence relative to the germline sequence |
substitutions |
Number of nucleotide substitutions in the read sequence relative to the germline sequence |
stop_codon |
True if a stop codon is present in the read sequence |
mutated_invariant |
True if a codon for a conserved amino acid is mutated in the read sequence |
inverted |
True if the read sequence is a reverse-complement to a germline gene segment |
out_frame_indel |
True if an insertion or deletion resulted in a frame shift |
out_frame_vdj |
True if the V(D)J recombination occurred out of frame |