Table 2.
Indels and frameshifts with high or moderate impact and above the prevalence filter (>15%/<85%).
| UniProt BLAST annotation | General information | PROVEAN | GO term | SnpEff annotation | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Protein name | UniProt acc. no. | Prev. | % prot. | Prediction | No. | Asp. | Info | Variant | Cat. | Annotation (effect) | Put. imp. |
| Uncharacterized protein | A0A1G5IYU0 | 48% | 87% | Neutral | No GO | – | – | p.Leu252_Glu253insAla | I | Disruptive_inframe_insertion | M |
| Gamma-glutamylputrescine oxidoreductase | A0A1F0J8L6 | 20% | 1% | Neutral | GO:0016491 | F | Oxido-reductase activity | p.Thr4_Ser5insProTyrPro | I | Conservative_inframe_insertion | M |
| 1% | na | p.Ser5fs | FS | Frameshift_variant | H | ||||||
Cluster 2: 2 indels and frameshifts.
Only indels and frameshifts above the prevalence filter (prevalence in at least 15% of strains) are reported. Variant annotation was performed by SnpEff. Protein function prediction was performed by PROVEAN with a cutoff of −2.5 (default).
“% of protein” (general information) = percent of total protein length before frameshift or termination; “variant category” (SnpEff): manually assigned based on HGVS.c/HGVS.p annotation; “HGVS.c & HGVS.p” = variant using HGVS (Human Genome Variation Society) notation with 1- or 3-letter amino acid code. Note that in case the variant is not coding, HGVS.p (protein level) is given instead of HGVS.c (DNA level).
UniProt BLAST annotation: the best hit (by identity) is given in the table.
prev., prevalence; % prot., % of protein; asp., aspect; cat., category; put. imp., putative impact; na, not applicable; UniProt acc. no.; UniProt accession number; no., number; I, indel (category); FS, frameshift (category); M, moderate (putative impact); H, high (putative impact).