Table 2.
VNII gene | CNAG | Variant type | CNAG function | Desjardins collection (13) | |||
---|---|---|---|---|---|---|---|
Sample | Lineage* | Variant type | Source | ||||
LQVO5_000317 | 00342 | Frameshift (270delC) | KOG: SWI–SNF chromatin-remodeling complex protein | 3 | VNI (1), VNII (1), and VNB (1) | Frameshift | Clinical |
LQVO5_004463 | 05940 | Premature stop codon lost (639A > T) | Pfam: ZFC3, zinc finger, C2H2 type | 24 | VNI (5) and VNB (19) | Frameshift | Clinical (50%) and environmental (50%) |
*Strain frequency for each lineage is listed in parentheses.