| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g28460 | A10 | 21805841 | C | T | missense_variant | MODERATE | c.131C>T|p.Ala44Val |
S19 |
| 2 | BAA10g28460 | A10 | 21806003 | C | T | missense_variant | MODERATE | c.293C>T|p.Pro98Leu |
S40 S49 |
| 3 | BAA10g28460 | A10 | 21807202 | C | T | missense_variant | MODERATE | c.1322C>T|p.Ser441Phe |
S257 |
| 4 | BAA10g28460 | A10 | 21807297 | C | T | synonymous_variant | LOW | c.1417C>T|p.Leu473Leu |
S185 |
| 5 | BAA10g28460 | A10 | 21807874 | A | C | intron_variant | MODIFIER | c.1663+254A>C| |
S116 S45 |
| 6 | BAA10g28460 | A10 | 21808248 | G | A | missense_variant | MODERATE | c.1724G>A|p.Gly575Glu |
S7 |
| 7 | BAA10g28460 | A10 | 21809550 | G | A | downstream_gene_variant | MODIFIER | c.*79G>A| |
S264 |
| 8 | BAA10g28460 | A10 | 21810560 | C | T | downstream_gene_variant | MODIFIER | c.*1089C>T| |
S236 |