| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g28840 | A10 | 21952969 | C | T | synonymous_variant | LOW | c.633G>A|p.Leu211Leu |
S98 |
| 2 | BAA10g28840 | A10 | 21953100 | C | T | missense_variant | MODERATE | c.502G>A|p.Gly168Ser |
S142 |
| 3 | BAA10g28840 | A10 | 21953374 | G | A | splice_region_variant&intron_variant | LOW | c.232-4C>T| |
S181 |
| 4 | BAA10g28840 | A10 | 21953634 | C | T | synonymous_variant | LOW | c.120G>A|p.Gln40Gln |
S48 |
| 5 | BAA10g28840 | A10 | 21954147 | G | A | missense_variant | MODERATE | c.56C>T|p.Pro19Leu |
S245 |
| 6 | BAA10g28840 | A10 | 21955824 | C | T | upstream_gene_variant | MODIFIER | c.-1622G>A| |
S33 |
| 7 | BAA10g28840 | A10 | 21956094 | G | A | upstream_gene_variant | MODIFIER | c.-1892C>T| |
S203 S236 |
| 8 | BAA10g28840 | A10 | 21956374 | G | A | upstream_gene_variant | MODIFIER | c.-2172C>T| |
S245 |