TABLE 1.
Reference position | Type | Lengtha (bp) | Reference | Allele | Countb | Coveragec (×) | Frequency (%) | Overlapping annotationsd | Average quality of variante | Coding region change | Amino acid change |
---|---|---|---|---|---|---|---|---|---|---|---|
17 | SNV | 1 | T | A | 7,705 | 7,760 | 99.29 | 35.53 | |||
18578 | Deletion | 1 | A | 3,167 | 3,335 | 94.96 | Gene: LSDV026; CDS: LSDV026 | 35.73 | AOE47602.1:c.479del | AOE47602.1:p.Leu160fs | |
22772 | Insertion | 1 | A | 3,147 | 3,437 | 91.56 | 36.39 | ||||
28073 | Insertion | 1 | T | 1,806 | 3,916 | 46.12 | 35.85 | ||||
84168 | SNV | 1 | C | A | 3,457 | 3,486 | 99.17 | Gene: LSDV089; CDS: LSDV089 | 36.6 | AOE47665.1:c.48G > T | AOE47665.1:p.Leu16Phe |
89076 | SNV | 1 | G | T | 3,881 | 3,886 | 99.87 | Gene: LSDV094; CDS: LSDV094 | 36.11 | AOE47670.1:c.254C > A | AOE47670.1:p.Pro85His |
125083 | Deletion | 1 | A | 3,771 | 4,119 | 91.55 | 33.62 |
Number of nucleotides comprised by the variants.
Number of reads mapped to the position, including the variants.
Total number of reads mapped onto the variants.
CDS, coding DNA sequence.
Average read quality score of the bases supporting a variant.